Date of introduction01.07.89

This standard applies to sand used as a filler for monolithic, prefabricated concrete and iron concrete structures, as well as material for the corresponding types construction work, and establishes test methods.

1. General Provisions

1.1. The scope of application of the sand testing methods provided for in this standard is specified in the appendix.

1.2. Samples are weighed with an error of 0.1% by weight, unless otherwise specified in the standard.

1.3. Samples or weighed portions of sand are dried to constant weight in an oven at a temperature of (105 ± 5) °C until the difference between the results of two weighings is no more than 0.1% of the mass. Each subsequent weighing is carried out after drying for at least 1 hour and cooling for at least 45 minutes.

1.4. Test results are calculated to the second decimal place unless otherwise specified regarding the accuracy of the calculation.

1.5. The arithmetic mean of the parallel determinations provided for the corresponding method is taken as the test result.

1.6. The standard set of sand sieves includes sieves with round holes diameters 10; 5 and 2.5 mm and wire sieves with standard square cells No. 1.25; 063; 0315; 016; 005 according to GOST 6613 (sieve frames are round or square with a diameter or side side of at least 100 mm).

Note. The use of sieves with meshes No. 014 is allowed before equipping enterprises with sieves with meshes No. 016.

1.7. The temperature of the room in which the tests are carried out must be (25±10) °C. Before starting the test, the sand and water must be at a temperature corresponding to the air temperature in the room.

1.8. Water for testing is used in accordance with GOST 2874 or GOST 23732, if the standard does not provide instructions on the use of distilled water.

1.9. When using hazardous (caustic, toxic) substances as reagents, one should be guided by the safety requirements set out in the regulatory and technical documents for these reagents.

1.10. In the “Equipment” sections there are links to state standards. The use of similar imported equipment is permitted. The non-standard measuring instruments used, specified in the “Equipment” section, must undergo metrological certification in accordance with GOST 8.326.

________________________________________________________________________________

Official publication Reproduction is prohibited

Reissue with Changes

S. 2 GOST 8735-88

STATE STANDARD OF THE USSR UNION

SAND FOR CONSTRUCTION WORK

TEST METHODS

GOST 8735-88

(ST SEV 5446-85)
ST SEV 6317-88

STATE CONSTRUCTION COMMITTEE OF THE USSR

STATE STANDARD OF THE USSR UNION

SAND FOR CONSTRUCTION WORK

Methodstests

Sand for construction work.
Testing methods

GOST 8735-88

(ST SEV 5446-85)
ST SEV 6317-88

Date of introduction 01.07.89

Failure to comply with the standard is punishable by law

This standard applies to sand used as a filler for monolithic, prefabricated concrete and reinforced concrete structures, as well as materials for relevant types of construction work and establishes test methods.

1. GENERAL PROVISIONS

1.1. The scope of application of the sand testing methods provided for in this standard is specified in.

1.2. Samples are weighed with an error of 0.1% by weight, unless otherwise specified in the standard.

1.3. Samples or weighed portions of sand are dried to constant weight in an oven at a temperature of (105 ± 5)° Until the difference between the results of two weighings is no more than 0.1% of the mass. Each subsequent weighing is carried out after drying for at least 1 hour and cooling for at least 45 minutes.

1.4. Test results are calculated to the second decimal place unless otherwise specified regarding the accuracy of the calculation.

1.5. The arithmetic mean of the parallel determinations provided for the corresponding method is taken as the test result.

Non-standardized measuring instruments must undergo metrological certification in accordance with GOST 8.326-89.

(Changed edition. Amendment No. 2).

2. SAMPLING

2.1. During acceptance control at the manufacturing plant, spot samples are taken, from which, by mixing, one combined sample is obtained from the replacement products of each production line.

2.2. Selection of point samples from production lines transporting products to a warehouse or directly to vehicles is carried out by crossing the flow of material on a conveyor belt or in places where the flow of material differs using samplers or manually.

To check the quality of sand shipped directly at the quarry face, spot samples are taken during loading into vehicles.

The sampling interval for spot samples during manual sampling can be increased if the manufacturer produces products of stable quality. To establish an acceptable sampling interval, the coefficient of variation of the content of grains passing through a sieve with mesh No. 016 and the content of dust and clay particles is determined quarterly. To determine the coefficient of variation of these indicators during a shift, point samples weighing at least 2000 are taken every 15 minutes. For each point sample, the content of grains passing through a sieve with mesh No. 016 and the content of dust and clay particles are determined. Then the coefficients of variation of these indicators are calculated in accordance with GOST 8269.0-97.

Depending on the obtained maximum value of the coefficient of variation for the two indicators being determined, the following intervals for taking point samples during the shift are taken:

3 hours - with a coefficient of variation of the indicator up to 10%;

2 hours»»»»»15%.

(Changed edition, Amendment No. 2).

2.4. The mass of a spot sample at a sampling interval of 1 hour must be at least 1500 g. When increasing the sampling interval in accordance with clause, the mass of the selected spot sample must be increased at an interval of 2 hours - twice, at an interval of 3 hours - twice four times.

If, when sampling with a sampler, the mass of a single sample turns out to be less than the specified one by more than 100 g, then it is necessary to increase the number of samples taken to ensure that the combined sample mass is at least 10,000 g.

To quarter the sample (after mixing), the cone of material is leveled and divided into four parts by mutually perpendicular lines passing through the center. Any two opposite quarters are sampled. By successive quartering, the sample is reduced by two, four times, etc. until a sample with a mass corresponding to p. is obtained.

When conducting periodic tests, as well as during incoming inspection and when determining the properties of sand during geological exploration, the mass of the laboratory sample must ensure that all tests required by the standard are carried out. It is allowed to carry out several tests using one sample, if during the testing the determined properties of the sand do not change, and the mass of the laboratory sample must be at least twice the total mass required for testing.

2.7. For each test, an analytical sample is taken from the laboratory sample.

Samples are taken from the analytical sample in accordance with the test procedure.

2.8. For each laboratory sample intended for periodic testing in the central laboratory of the association or in a specialized laboratory, as well as for arbitration tests, a sampling report is drawn up, including the name and designation of the material, the place and date of sampling, the name of the manufacturer, the designation of the sample and the signature of the person in charge for collecting a facial sample.

The selected samples are packaged in such a way that the mass and properties of the materials do not change before testing.

Each sample is provided with two labels indicating the sample designation. One label is placed inside the package, the other is placed in a visible place on the package.

During transportation, the packaging must be protected from mechanical damage and getting wet.

2.9. To check the quality of sand extracted and laid by hydromechanization, the alluvium map is divided in plan along the length (along the alluvium map) into three parts.

From each part, spot samples are taken from at least five different places (in plan). To take a point sample, dig a hole 0.2-0.4 m deep. A sand sample is taken from the hole with a scoop, moving it from bottom to top along the wall of the hole.

From spot samples, a combined sample is obtained by mixing, which is reduced to obtain a laboratory sample according to paragraph .

The quality of sand is assessed separately for each part of the alluvium map based on the results of testing a sample taken from it.

2.10. When arbitrating the quality of sand in warehouses, point samples are taken using a scoop in places located evenly across the entire surface of the warehouse, from the bottom of dug holes 0.2-0.4 m deep. The holes should be placed in a checkerboard pattern. The distance between the wells should not exceed 10 m. The laboratory sample is prepared according to paragraph.

Based on the sifting results, the following is calculated: the partial residue on each sieve ( A i) as a percentage according to the formula

(3)

Where t i - mass of residue on a given sieve, g;

T -weight of the sample being sifted, g;

full residue on each sieve ( A i) as a percentage according to the formula

(4)

Where a 2,5 , a 1,25 , a i- partial residues on the corresponding sieves;

sand fineness modulus ( M j) without grains larger than 5 mm according to the formula

(5)

Where A 2,5 , A 1,25 ,A 063 , A 0315 , A 016 - complete residues on a sieve with round holes with a diameter of 2.5 mm and on sieves with mesh No. 1.25; 063; 0315, 016, %.

The result of determining the grain composition of sand is drawn up in accordance with table. or depicted graphically in the form of a sifting curve in accordance with the drawing. .

Screening curve

Residues, % by weight, on sieves

Pass through a sieve with mesh No. 016(014),
% by weight

0,16
(0,14)

A 016(014)

Drying cabinet.

Sieves with mesh No. 1.25 according to GOST 6613-86

Steel needle.

4.3. Preparing for the test

An analytical sample of sand is sifted through a sieve with holes with a diameter of 5 mm, at least 100 g of sand is taken from it, dried to a constant weight and scattered on sieves with holes with a diameter of 2.5 mm and a mesh No. 1.25. From the resulting sand fractions, samples are taken weighing:

5.0 g - fractions of St. 2.5 to 5 mm;

1.0 g - fractions from 1.25 to 2.5 mm

Each sample of sand is poured thin layer on glass or a metal sheet and moisten using a pipette. Clay lumps differing in viscosity are separated from the sample using a steel needle. from sand grains, using a magnifying glass if necessary. The sand grains remaining after separating the lumps are dried to a constant mass and weighed.

4.4.Processing the results

(6)

(7)

Where m 1 , m 2 - weight of a sample of sand fraction, respectively, from 2.5 to 5 mm and from 1.25 to 2.5 mm before the release of clay, g;

T 1 ;m 3 - mass of grains of sand fractions respectively from 2.5 to 5 mm and from 1.25 to 2.5 mm after the release of clay, g.

(8)

Where A 2,5 , A 1.25 - partial residues as a percentage by weight on sieves with openings of 2.5 and 1.25 mm, calculated according to paragraph.

5. DETERMINATION OF THE CONTENT OF DUST AND CLAY PARTICLES

5.1. Elutriation method

5.1.1. Essence of the method

Drying cabinet.

A cylindrical bucket with a height of at least 300 mm with a siphon or a vessel for removing sand (drawing).

Stopwatch according to GOST 5072-79.

(Changed edition, Amendment No. 2).

5.1.3. Preparing for the test

An analytical sample of sand is sifted through a sieve with holes 5 mm in diameter, the sand that has passed through the sieve is dried to a constant weight and a sample weighing 1000 g is taken from it.

5.1.4. Carrying out the test

A sample of sand is placed in a cylindrical bucket and filled with water so that the height of the water layer above the sand is about 200 mm. The sand filled with water is kept for 2 hours, stirring it several times, and thoroughly washed to remove clay particles adhering to the grains.

After this, the contents of the bucket are vigorously mixed again and left alone for 2 minutes. After 2 minutes, siphon off the suspension obtained during washing, leaving a layer of it above the sand at least 30 mm high. Then the sand is again filled with water to the level indicated above. Washing the sand in the specified sequence is repeated until the water remains clear after washing.

When using a vessel for elutriation, the test is carried out in the same sequence. In this case, water is poured into the vessel to the top drain hole, and the suspension is drained through the two lower holes.

After elutriation, the washed sample is dried to constant weight. T 1 .

5.1.5. Processing the results

(9)

Where T - mass of the dried sample before elutriation, g;

m 1 - mass of the dried sample after elutriation, g.

Vessel for elutriation

The bucket is cylindrical with two marks (belts) on the inner wall, corresponding to a capacity of 5 and 10 liters.

The bucket is cylindrical without marks.

Drying cabinet.

Sieves with mesh No. 063 and 016 according to GOST 6613-86.

Metal cylinders with a capacity of 1000 ml with an observation window (2 pcs.).

Metal measuring pipette with a capacity of 50 ml (drawing).

Funnel with a diameter of 150 mm.

Stopwatch according to GOST 5072-79

Cup or glass for evaporation according to GOST 9147-80.

(Changed edition, Amendment No. 2).

5.2.3. Carrying out the test

A sample of sand weighing about 1000 g can be natural humidity weighed, placed in a bucket (without a label) and filled with 4.5 liters of water. In addition, prepare about 500 ml of water for subsequent rinsing of the bucket.

The sand filled with water is kept for 2 hours, stirring it several times, and thoroughly washed to remove clay particles adhering to the grains. Then the contents of the bucket are carefully poured onto two sieves: the upper one with mesh No. 063 and the lower one with mesh No. 016, placed on the bucket with marks.

The suspension is allowed to settle and the clarified water is carefully poured into the first bucket. With the drained water, the sand is washed a second time on sieves over a second bucket (with marks). After this, the first bucket is rinsed with the remaining water and this water is poured into the second bucket. In this case, such an amount of water is used so that the level of the suspension in the latter reaches exactly the 5 liter mark; if the remaining water is not enough for this, the volume of the suspension is adjusted to 5 liters by adding additional water.

After this, the suspension is thoroughly mixed in a bucket and immediately filled with it using a funnel, alternately, into two metal cylinders with a capacity of 1000 ml, while continuing to mix the suspension. The suspension level in each cylinder must correspond to the mark on the inspection window.

The suspension in each cylinder is stirred with a glass or metal rod or the cylinder is tilted several times, closing it with a lid, for better mixing.

After mixing is completed, leave the cylinder alone for 1.5 minutes. 5-10 s before the end of the holding period, lower the measuring pipette with the tube closed with a finger into the cylinder so that the support cover rests on the top of the cylinder wall, while the bottom of the pipette will be at the level of suspension selection - 190 mm from the surface. After the specified time has elapsed (5-10 s), open the pipette tube and, after filling it, close the tube again with your finger, remove the pipette from the cylinder and, having opened the tube, pour the contents of the pipette into a pre-weighed cup or glass. The filling of the pipette is monitored by changes in the level of the suspension in the viewing window.

Metal cylinder and measuring pipette

5.3. Wet sieving method

The test is carried out according to GOST 8269.0-97, using a sample of sand weighing 1000 g and sieves with mesh No. 0315 and 005.

(Changed edition, Amendment No. 2).

5.4. Photoelectric method

The method is based on comparing the degree of transparency clean water and suspension obtained by washing sand.

The test is carried out according to GOST 8269.0-97, using a sample of sand weighing 1000 g.

(Changed edition, Amendment No. 2).

5.5. The content of dust and clay particles can be determined using one of the above methods, depending on the availability of equipment. In this case, the elutriation method is allowed to be used until 01/01/95.

6. DETERMINATION OF THE PRESENCE OF ORGANIC IMPURITIES

6.1. Essence of the method

The presence of organic impurities (humic substances) is determined by comparing the color of the alkaline solution over the sand sample with the color of the standard.

Photocolorimeter FEK-56M or spectrophotometer SF-4, or other similar devices.

Glass cylinders with a capacity of 250 ml made of transparent colorless glass (internal diameter 36-40 mm) in accordance with GOST 1770-74.

Water bath.

Sodium hydroxide (sodium hydroxide) according to GOST 4328-77, 3% solution.

Tannin, 2% solution in 1% ethanol.

(Changed edition, Amendment No. 2).

6.3. Preparing for the test

From an analytical sample of sand in a state of natural moisture, take a sample of about 250 g.

Prepare a standard solution by dissolving 2.5 ml of a 2% tannin solution in 97.5 ml of a 3% sodium hydroxide solution. The prepared solution is stirred and left for 24 hours.

The optical density of the tannin solution, determined on a photocolorimeter or spectrophotometer in the wavelength region of 450-500 nm, should be 0.60-0.68.

6.4. Carrying out the test

Fill a measuring cylinder with sand to a level of 130 ml and fill it with a 3% sodium hydroxide solution to a level of 200 ml. The contents of the cylinder are stirred and left for 24 hours, repeating the stirring 4 hours after the first stirring. Then the color of the liquid settled over the sample is compared with the color of the standard solution or glass, the color of which is identical to the color of the standard solution.

Sand is suitable for use in concrete or mortars if the liquid above the sample is colorless or is significantly less colored than the reference solution.

If the color of the liquid is slightly lighter than the standard solution, the contents of the vessel are heated for 2-3 hours in a water bath at a temperature of 60-70 ° C and the color of the liquid above the sample is compared with the color of the standard solution.

If the color of the liquid is the same or darker than the color of the reference solution, it is necessary to test the aggregate in concrete or solutions in specialized laboratories.

7. DETERMINATION OF MINERALOGICAL-PETROGRAPHIC COMPOSITION

7.1. Essence of the method

Set of sieves with mesh No. 1.25; 063; 0315 and 016 according to GOST 6613-86 and with round holes with diameters of 5 and 2.5 mm.

Drying cabinet.

Binocular microscope with magnification from 10 to 50 C , polarizing microscope with magnification up to 1350 C .

Mineralogical magnifying glass according to GOST 25706-83.

Set of reagents.

Steel needle.

(Changed edition, Amendment No. 2).

7.3. Preparing for the test

An analytical sand sample is sifted through a sieve with holes 5 mm in diameter, and at least 500 g of sand is taken from the sifted part of the sample.

The sand is washed, dried to a constant weight, scattered on a set of sieves with holes with a diameter of 2.5 mm and mesh No. 1.25; 063; 0315; 016 and select samples weighing at least:

25.0 g - for sand with grain size. 2.5 to 5.0 mm;

5.0 g"""""St. 1.25 to 2.5 mm;

1.0 g"""""St. 0.63 to 1.25 mm;

0.1 g"""""St. 0.315 to 0.63 mm;

0.01 g»»»»» from 0.16 to 0.315 mm.

7.4. Carrying out the test

Each sample is poured in a thin layer onto glass or paper and viewed using a binocular microscope or magnifying glass.

Sand grains, represented by fragments of the corresponding rocks and minerals, are separated using a thin needle into groups according to rock types and types of minerals.

If necessary, the identification of rocks and minerals is clarified using chemical reagents (hydrochloric acid solution, etc.), as well as by analysis in immersion liquids using a polarizing microscope.

In sand grains, represented by mineral fragments, the content of quartz, feldspar, dark-colored minerals, calcite, etc. is determined.

Sand grains, represented by rock fragments, are divided into genetic types in accordance with Table. .

table 2

In addition, grains of rocks and minerals classified as harmful impurities are isolated in the sand.

These rocks and minerals include: containing amorphous varieties of silicon dioxide (chalcedony, opal, flint, etc.); sulfur; sulfides (pyrite, marcasite, pyrrhotite, etc.); sulfates (gypsum, anhydrite, etc.); layered silicates (micas, hydromicas, chlorites, etc.); iron oxides and hydroxides (magnetite, goethite, etc.); apatite; nepheline; phosphorite; halogen compounds (halite, sylvite, etc.); zeolites; asbestos; graphite; coal; oil shale.

In the presence of minerals containing sulfur, the amount of sulfate and sulfide compounds in terms of SO 3 determined by item.

The same samples of sand are used to determine the shape and nature of the surface of sand grains in accordance with Table. .

Table 3

7.5. Processing the results

For each type of isolated rocks and minerals, the number of grains is counted and their content is determined ( X) as a percentage in a sample according to the formula

(14)

Where n - the number of grains of a given rock or mineral;

N- total number grains in the test sample.

8. DETERMINATION OF TRUE DENSITY

8.1. Pycnometric method

8.1.1. Essence of the method

True density is determined by measuring the mass per unit volume of dried sand grains.

Piconometer with a capacity of 100 ml according to GOST 22524-77.

Desiccator according to GOST 25336-82.

Drying cabinet.

Sand bath or water bath.

Distilled water according to GOST 6709-72.

GOST 450-77.

(Changed edition, Amendment No. 2).

8.1.3. Preparing for the test

A sample of about 30 g is taken from an analytical sand sample, sifted through a sieve with holes 5 mm in diameter, dried to a constant weight and cooled to room temperature in a desiccator over concentrated sulfuric acid or anhydrous calcium chloride. The dried sand is mixed and divided into two parts.

8.1.4. Carrying out the test

Each part of the sample is poured into a clean, dried and pre-weighed pycnometer, after which it is weighed along with the sand. Then distilled water is poured into the pycnometer in such an amount that the pycnometer is filled to approximately 2/3 of its volume, the contents are mixed and placed in a slightly inclined position on a sand bath or water bath. The contents of the pycnometer are boiled for 15-20 minutes to remove air bubbles; Air bubbles can also be removed by keeping the pycnometer under vacuum in a desiccator.

After removing the air, the pycnometer is wiped, cooled to room temperature, topped up to the mark with distilled water and weighed. After this, the pycnometer is emptied of its contents, washed, filled to the mark with distilled water and weighed again. All weighings are carried out with an error of up to 0.01 g.

8.1.5. Processing the results

The true density of sand (r) in g/cm 3 is calculated using the formula

Le Chatelier device (drawing).

Weighing glass or porcelain cup according to GOST 9147-80.

Desiccator according to GOST 25336-82.

Drying cabinet.

Sieve with round holes 5 mm.

Sulfuric acid according to GOST 2184-77.

Calcium chloride (calcium chloride) according to GOST 450-77.

(Changed edition, Amendment No. 2).

Le Chatelier device

A sieve with round holes with a diameter of 5 mm.

(Changed edition, Amendment No. 2).

9.1.3. Preparing for the test

9.1.3.1. When determining bulk density in a standard uncompacted state during incoming inspection, tests are carried out in measured quantities cylindrical vessel with a capacity of 1 liter, using about 5 kg of sand, dried to a constant mass and sifted through a sieve with round holes with a diameter of 5 mm.

9.1.3.2. When determining the bulk density of sand in a batch to convert the amount of sand supplied from mass units to volumetric units at. Acceptance control tests are carried out in a measuring cylindrical vessel with a capacity of 10 liters. Sand is tested in a state of natural moisture without sifting through a sieve with holes 5 mm in diameter.

9.1.4. Carrying out the test

9.1.4.1. When determining the bulk density of sand in a standard uncompacted state, sand is scooped into a pre-weighed measuring cylinder from a height of 10 cm from the top edge until a cone forms above the top of the cylinder. The cone without sand compaction is removed flush with the edges of the vessel with a metal ruler, after which the vessel with sand is weighed.

9.1.4.2. When determining the bulk density of sand in a batch to convert the amount of sand supplied from mass units to volumetric units, sand is scooped into a pre-weighed measuring cylinder from a height of 100 cm from the top edge of the cylinder until a cone forms above the top of the cylinder. The cone without sand compaction is removed flush with the edges of the vessel with a metal ruler, after which the vessel with sand is weighed.

Bulk density of sand (r n ) in kg/m3 is calculated using the formula

(18)

Where T - mass of the measuring vessel, kg;

T 1 - mass of the measuring vessel with sand, kg;

V-volume of the vessel, m3.

Determination of the bulk density of sand is carried out twice, each time taking a new portion of sand.

Note. The bulk density of the sand-gravel mixture is determined according to GOST 8269-87.

9.2. Definition of voidness

The voidness (volume of intergranular voids) of sand in a standard uncompacted state is determined based on the values true density and bulk density of sand, previously established according to paragraphs. And .

Emptiness of sand (V m.p ) as a percentage by volume is calculated using the formula

(19)

Where r - true density of sand, g/cm 3 ;

r n - bulk density of sand, kg/m3.

10. DETERMINATION OF HUMIDITY

10.1. Essence of the method

Humidity is determined by comparing the mass of sand in a state of natural humidity and after drying.

Drying cabinet.

Baking tray.

(Changed edition, Amendment No. 2).

10.3. Carrying out the test

A sample weighing 1000 g of sand is poured into a baking sheet and immediately weighed, and then dried in the same baking sheet to a constant weight.

10.4. Processing the results

Sand moisture (W) as a percentage is calculated using the formula

(20)

Where T - weight of the sample in a state of natural humidity;

T 1 - weight of the sample in dry condition, g.

11. DETERMINATION OF REACTIVITY

The test is carried out in accordance with GOST 8269-87, using a sample of sand weighing at least 250 g.

12. DETERMINATION OF THE CONTENT OF SULPHATE AND SULPHIDE COMPOUNDS

12.1. To determine the content of harmful sulfur-containing impurities in sand, the total sulfur content is determined, then the sulfate sulfur content is determined, and the sulfide sulfur content is calculated from their difference.

If only sulfate compounds are present in the sand, the total sulfur content is not determined.

12.2. Determination of total sulfur content

12.2.1. Weight method

12.2.1.1. Essence of the method

Weight method is based on the decomposition of a sample with a mixture of nitric and hydrochloric acids, followed by the precipitation of sulfur in the form barium sulfate and determining the mass of the latter.

The furnace is a muffle furnace, providing a heating temperature of 900 °C.

Porcelain cups with a diameter of 15 cm according to GOST 9147-80.

Glass glasses with a capacity of 100, 200 300 400 ml according to GOST 23932-90.

Porcelain crucibles according to GOST 9147-80.

Desiccator according to GOST 25336-82.

Water bath.

Calcium chloride (calcium chloride) according to GOST 450-77, calcined at a temperature of 700-800 °C.

Ash paper filters according to TU 6-09-1706-82.

Nitric acid according to GOST 4461-77.

Hydrochloric acid according to GOST 3118-77.

Aqueous ammonia according to GOST 3760-79, 10% solution.

Barium chloride (barium chloride) according to GOST 4108-72, 10% solution.

Methyl orange according to TU 6-09-5169-84, 0.1% solution.

Silver nitrate (silver nitrate) according to GOST 1277-75, 1% solution.

Wire woven sieves with square cells No. 005 and 0071 according to GOST 6613-86.

(Changed edition, Amendment No. 2).

An analytical sample of sand is sifted through a sieve with holes with a diameter of 5 mm and 100 g of sand is taken from the sifted part, which is crushed to the size of particles passing through a sieve with mesh No. 016, a sample weighing 50 g is taken from the resulting sand. The selected sample is ground again to particle size passing through sieve No. 0071.

The crushed sand is dried to a constant weight, placed in a bottle, stored in a desiccator over calcined calcium chloride, and samples are taken from it for analysis ( T) weighing 0.5-2 g.

The sample, weighed with an accuracy of 0.0002 g, is placed in a glass beaker with a capacity of 200 ml or a porcelain cup, moistened with a few drops of distilled water, 30 ml of nitric acid is added, covered with glass and left for 10-15 minutes. After the reaction is complete, add 10 ml of hydrochloric acid, stir with a glass rod, cover with glass and place the glass or cup in a water bath. 20-30 minutes after the release of brown vapors of nitrogen oxides ceases, the glass is removed and the contents of the glass or cup are evaporated to dryness. After cooling, the residue is moistened with 5-7 ml of hydrochloric acid and again evaporated to dryness. The operation is repeated 2-3 times, adding 50 ml hot water and boil until the salts are completely dissolved.

To precipitate elements of the sesquioxide group, add 2-3 drops of methyl orange indicator to the solution and add ammonia solution until the color of the solution changes from red to yellow and the smell of ammonia appears. After 10 minutes, the coagulated sesquioxide precipitate is filtered through a “red ribbon” filter into a glass with a capacity of 300-400 ml. The precipitate is washed warm water with the addition of a few drops of ammonia solution. Hydrochloric acid is added to the filtrate until the color of the solution changes to pink color and add another 2.5 ml of acid.

The filtrate is diluted with water to a volume of 200-250 ml, heated to a boil, 10 ml of a hot barium chloride solution is poured into it at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense filter " blue tape" and washed 10 times in small portions cold water until chloride ions are removed.

After cooling in the desiccator, the crucible with the sediment is weighed. Calcination is repeated until a constant mass is obtained. To determine the sulfur content in the reagents used for analysis, a “blind experiment” is carried out in parallel with the analysis. The amount of barium sulfate found by "deaf experiment" T 2, subtracted from the mass of barium sulfate T 1 obtained from sample analysis.

Note. The expression “blind experiment” means that the test is carried out in the absence of the test object, using the same reagents and observing all experimental conditions.

Total sulfate sulfur content ( X 1) as a percentage based on SO 3 calculated by the formula

Permissible discrepancy, abs. %

St. 0.5 to 1.0

12.2.2. Iodometric titration method

12.2.2.1. Essence of the method

The method is based on burning a sample in a flow of carbon dioxide at a temperature of 1300-1350 °C, absorbing the released SO 2 iodine solution and titration with sodium thiosulfate solution of excess iodine that has not reacted with the resulting sulfurous acid.

Sodium thiosulfate according to GOST 27068-86, 0.005 n. solution.

Sodium carbonate (sodium carbonate) according to GOST 83-79.

Potassium dichromate (potassium dichromate) according to GOST 4220-75, fixanal.

Soluble starch according to GOST 10163-76, 1.0% solution.

Iodine according to GOST 4159-79, 0.005 N solution.

Potassium iodide (potassium iodide) according to GOST 4232-74.

Sulfuric acid according to GOST 4204-77, 0.1 N solution.

Analytical balance, measurement error 0.0002 g.

To prepare a solution of sodium thiosulfate, dissolve 1.25 g Na2S2O3 · 5 H 2 O in 1 liter of freshly boiled distilled water and add 0.1 g of sodium carbonate. The solution is stirred and left for 10-12 days, after which its titer is determined using a 0.01 N solution of potassium dichromate prepared from fixanal.

To 10 ml of a 0.01 N solution of potassium dichromate, add 50 ml of a 0.1 N solution of sulfuric acid, 2 g of dry potassium iodide and titrate with the prepared sodium thiosulfate solution until the color is straw-yellow. Add a few drops of 1% starch solution (the solution is colored Blue colour) and titrate until the solution becomes colorless. Correction factor for the titer of 0.005 N sodium thiosulfate solution determined by the formula

(22)

Where - normality of the potassium dichromate solution;

10 - volume of 0.01 N solution of potassium bichromate taken for titration, ml;

V-volume of 0.005 N sodium thiosulfate solution used for titration of 10 ml of 0.01 N solution of potassium dichromate, ml;

Normality of sodium thiosulfate solution.

The titer is checked at least once every 10 days.

The sodium thiosulfate solution is stored in dark bottles.

To prepare an iodine solution, 0.63 g of crystalline iodine and 10 g of potassium iodide are dissolved in 15 ml of distilled water. The solution is transferred to a 1-liter volumetric flask with a well-ground stopper, topped up with water to the mark, mixed and stored in the dark.

The titer of the prepared iodine solution is determined using a titrated solution of sodium thiosulfate prepared in the manner described above (p.).

10 ml of 0.005 N iodine solution is titrated with 0.005 N sodium thiosulfate solution in the presence of starch.

The correction factor for the titer of 0.005 N iodine solution () is determined by the formula

(23)

Where - volume of 0.005 N sodium thiosulfate solution used for titrating the iodine solution, ml;

Correction factor 0.005 N sodium thiosulfate solution;

- normality of iodine solution;

10 - amount of iodine solution taken for titration, ml.

12.2.2.5. Preparing for the test

Samples for testing are prepared according to clause 12.1.1.3, with the weight of the samples taken equal to 0.1-1.0 g.

Before starting work, heat the furnace to a temperature of 1300 °C and check the tightness of the installation. To do this, close the tap in front of the absorption vessel and let in carbon dioxide. The cessation of gas bubbles passing through the flushing flask indicates the tightness of the installation.

Determine the coefficient TO, establishing the relationship between the concentrations of iodine solution and sodium thiosulfate. Carbon dioxide is passed through the installation for 3-5 minutes, and the absorption vessel is filled 2/3 with water. 10 ml of titrated iodine solution is poured from a burette, 5 ml of 1.0% starch solution is added and titrated with sodium thiosulfate solution until the solution becomes colorless. Ratio of concentrations of solutions of iodine and sodium thiosulfate TO is taken equal to the average value of three determinations. Concentration ratio coefficient TO in laboratory conditions is determined daily before testing.

12.2.2.6. Testing

The sample, weighed to the nearest 0.0002 g, is placed in a pre-heated boat. 250-300 ml of distilled water are poured into the absorption vessel, the volume of iodine solution measured with a burette, 5 ml of starch solution are added and mixed with a stream of carbon dioxide.

Installation diagram for determining sulfur content

To carry out the analysis, use equipment and reagents in solutions specified in paragraph , using hydrochloric acid in accordance with GOST 3118-77, solution 1:3 (one part by volume of concentrated hydrochloric acid and three parts by volume of water).

12.3.3. Preparing for the test

The sample for testing is prepared according to clause 12.1.1.3, with the mass of the sample being taken equal to 1 g.

12.3.4. Testing

Weighed T place in a glass with a capacity of 100-150 ml, cover with glass and add 40-50 ml of hydrochloric acid. After the release of gas bubbles stops, place the glass on the stove and keep it at a low boil for 10-15 minutes. Sesquioxides are precipitated by adding 2-3 drops of methyl orange indicator and adding ammonia solution until the color of the indicator changes from red to yellow and the smell of ammonia appears. After 10 minutes, the precipitate is filtered off. The precipitate is washed with warm water with the addition of a few drops of ammonia solution.

The filtrate is neutralized hydrochloric acid until the color of the solution turns pink and add another 2.5 ml of acid. The solution is heated to a boil and 10 ml of a hot barium chloride solution is added at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense blue ribbon filter and washed 10 times with small portions of cold water until chloride ions are removed.

The complete removal of chloride ions is checked by reaction with silver nitrate: a few drops of the filtrate are placed on glass and a drop of 1% silver nitrate solution is added. The absence of the formation of a white precipitate indicates the complete removal of chloride ions.

The precipitate with a filter is placed in a porcelain crucible, pre-calcined to constant weight at a temperature of 800-850 °C, dried, ashed, avoiding ignition of the filter, and calcined in an open crucible until the filter completely burns out, and then at a temperature of 800-850 °C in for 30-40 minutes.

After cooling in the desiccator, the crucible with the sediment is weighed. Calcination is repeated until a constant mass is obtained.

In parallel with the analysis, a “deaf experiment” is carried out (see note to paragraph). Barium sulfate quantity T 2, found by “deaf experiment”, is subtracted from the mass of barium sulfate T 1 obtained from sample analysis.

12.3.5. Processing the results

Acceptable discrepancies between the results of two parallel analyzes are accepted according to clause.

12.4. Determination of sulfide sulfur content

(27)

Where X - total sulfur content in terms of SO 3,%;

X 1 - content of sulfate sulfur in terms of SO 3,%.

13. DETERMINATION OF FROST RESISTANCE OF SAND FROM CRUSHING SEEDS

13.1. Essence of the method

The frost resistance of sand is determined by the loss of mass during successive freezing and thawing.

Freezer chamber.

Drying cabinet.

Sieves with mesh No. 1.25; 016 according to GOST 6613-86 and with round holes with a diameter of 5 mm.

Vessel for thawing samples.

Fabric bags made of thick fabric with double walls.

Baking trays.

(Changed edition, Amendment No. 2).

13.3.Sample preparation

The laboratory sample is reduced to a mass of at least 1000 g, sifted on two sieves: the first with holes with a diameter of 5 mm and the second with mesh No. 1.25 or 016, depending on the size of the material being tested, dried to a constant weight, after which two samples are taken weighing 400 g.

13.4.Testing

Each sample is placed in a bag that ensures the safety of the grains, immersed in a vessel with water to saturate for 48 hours. The bag with the sample is removed from the water and placed in freezer, providing a gradual decrease in temperature to minus (20±5) °C.

The samples are kept in a chamber at a steady temperature of minus (20±5) °C for 4 hours, after which the bags with samples are removed, immersed in a vessel with water at a temperature of 20 °C, and kept for 2 hours.

STATE STANDARD OF THE USSR UNION

SAND FOR CONSTRUCTION WORK

TEST METHODS

GOST 8735-88

(ST SEV 5446-85)
ST SEV 6317-88

STATE CONSTRUCTION COMMITTEE OF THE USSR

STATE STANDARD OF THE USSR UNION

SAND FOR CONSTRUCTION WORK

Methodstests

Sand for construction work.
Testing methods

GOST 8735-88

(ST SEV 5446-85)
ST SEV 6317-88

Date of introduction 01.07.89

Failure to comply with the standard is punishable by law

This standard applies to sand used as a filler for monolithic concrete, prefabricated concrete and reinforced concrete structures, as well as material for corresponding types of construction work and establishes test methods.

1. GENERAL PROVISIONS

1.1. The scope of application of the sand testing methods provided for in this standard is specified in.

1.2. Samples are weighed with an error of 0.1% by weight, unless otherwise specified in the standard.

1.4. Test results are calculated to the second decimal place unless otherwise specified regarding the accuracy of the calculation.

1.5. The arithmetic mean of the parallel determinations provided for the corresponding method is taken as the test result.

Non-standardized measuring instruments must undergo metrological certification in accordance with GOST 8.326-89.

(Changed edition. Amendment No. 2).

2. SAMPLING

2.1. During acceptance control at the manufacturing plant, spot samples are taken, from which, by mixing, one combined sample is obtained from the replacement products of each production line.

To check the quality of sand shipped directly at the quarry face, spot samples are taken during loading into vehicles.

Depending on the obtained maximum value of the coefficient of variation for the two indicators being determined, the following intervals for taking point samples during the shift are taken:

3 hours - with a coefficient of variation of the indicator up to 10%;

2 hours » » » » » 15%.

(Changed edition, Amendment No. 2).

2.7. For each test, an analytical sample is taken from the laboratory sample.

Samples are taken from the analytical sample in accordance with the test procedure.

The selected samples are packaged in such a way that the mass and properties of the materials do not change before testing.

Each sample is provided with two labels indicating the sample designation. One label is placed inside the package, the other is placed in a visible place on the package.

During transportation, the packaging must be protected from mechanical damage and wetness.

2.9. To check the quality of sand extracted and laid by hydromechanization, the alluvium map is divided in plan along the length (along the alluvium map) into three parts.

From spot samples, a combined sample is obtained by mixing, which is reduced to obtain a laboratory sample according to paragraph .

The quality of sand is assessed separately for each part of the alluvium map based on the results of testing a sample taken from it.

2.12. During geological exploration, samples are taken in accordance with regulatory and technical documentation approved in the prescribed manner.

3. DETERMINATION OF GRAIN COMPOSITION AND FINANCY MODULE

3.1. Essence of the method

The grain composition is determined by sifting sand on a standard set of sieves.

Based on the sifting results, the following is calculated: the partial residue on each sieve ( Ai) as a percentage according to the formula

Where ti - mass of residue on a given sieve, g;

T - weight of the sample being sifted, g;

full residue on each sieve ( Ai) as a percentage according to the formula

Where a 2,5, a 1,25, ai- partial residues on the corresponding sieves;

sand fineness modulus ( M j) without grains larger than 5 mm according to the formula

(5)

Where A 2,5, A 1,25,A 063, A 0315, A 016 - complete residues on a sieve with round holes with a diameter of 2.5 mm and on sieves with mesh No. 1.25; 063; 0315, 016, %.

The result of determining the grain composition of sand is drawn up in accordance with table. or depicted graphically in the form of a sifting curve in accordance with the drawing. .

Screening curve

Table 1

Residues, % by weight, on sieves

Pass through a sieve with mesh No. 016(014),
% by weight

0,16
(0,14)

A 016(014)

Drying cabinet.

5. DETERMINATION OF THE CONTENT OF DUST AND CLAY PARTICLES

5.1. Elutriation method

5.1.1. Essence of the method

Drying cabinet.

A cylindrical bucket with a height of at least 300 mm with a siphon or a vessel for removing sand (drawing).

Stopwatch according to GOST 5072-79.

5.1.3. Preparing for the test

5.1.4. Carrying out the test

When using a vessel for elutriation, the test is carried out in the same sequence. In this case, water is poured into the vessel up to the upper drain hole, and the suspension is drained through the two lower holes.

After elutriation, the washed sample is dried to constant weight. T 1.

5.1.5. Processing the results

(9)

Where T - mass of the dried sample before elutriation, g;

m 1 - mass of the dried sample after elutriation, g.

Vessel for elutriation

Notes:

1. When testing natural sands, the grains of which are tightly cemented with clay, the sample is kept in water for less than 1 day.

2. It is allowed to test sand in a state of natural moisture. In this case, the moisture content of the sand and the content of dust and clay particles are determined in a parallel sample ( P otm) is calculated as a percentage using the formula

(10)

Where T c is the mass of the sample in a state of natural humidity, g;

T 1 - mass of sample dried after elutriation to constant mass, g;

W- moisture content of the tested sand, %.

5.2. Pipette method

5.2.1. Essence of the method

The bucket is cylindrical with two marks (belts) on the inner wall, corresponding to a capacity of 5 and 10 liters.

The bucket is cylindrical without marks.

Drying cabinet.

Metal cylinders with a capacity of 1000 ml with an observation window (2 pcs.).

Metal measuring pipette with a capacity of 50 ml (drawing).

Funnel with a diameter of 150 mm.

Stopwatch according to GOST 5072-79

Cup or glass for evaporation according to GOST 9147-80.

(Changed edition, Amendment No. 2).

5.2.3. Carrying out the test

A sample of sand weighing about 1000 g in a state of natural humidity is weighed, placed in a bucket (without a mark) and filled with 4.5 liters of water. In addition, prepare about 500 ml of water for subsequent rinsing of the bucket.

The suspension in each cylinder is stirred with a glass or metal rod or the cylinder is tilted several times, closing it with a lid, for better mixing.

Metal cylinder and measuring pipette

1 - cylinder; 2 - pipette; 3 - label (1000 ml); 4 - suspension level in the cylinder

Instead of metal cylinders with a viewing window and a special pipette, it is allowed to use ordinary glass measuring cylinders with a capacity of 1 liter and a glass pipette with a capacity of 50 ml, lowering it into the cylinder to a depth of 190 mm.

The suspension in a cup (glass) is evaporated in a drying cabinet at a temperature of (105±5) °C. The cup (glass) with the evaporated powder is weighed on a scale with an error of up to 0.01 g. A suspension sample is taken from the second cylinder in the same way.

5.2.4. Processing the results

Where T - weight of a sample of sand, g;

T 1 - mass of a cup or glass for evaporating the suspension, g;

T 2 - weight of a cup or glass with evaporated powder, g.

In the case of testing sand that is heavily contaminated with dust and clay particles, the volume of water for washing is taken equal to 10 liters instead of 5 liters. Accordingly, increase the volume of the suspension in a bucket with marks to 10 liters. In this case, the test result ( P otm) as a percentage calculated by the formula

(12)

Note. Allowed mass of sediment ( T 2-T 1) determined by the density of the suspension using the formula

(13)

Where T 3 - mass of pycnometer with suspension, g;

T 4 - mass of pycnometer with water, g;

r - sediment density, g/cm3 (assumed equal to 2.65 g/cm3).

The result of determining the mass of sediment T 2-T 1 is entered into formula ().

5.3. Wet sieving method

The method is based on comparing the degree of transparency of pure water and the suspension obtained by washing sand.

Photocolorimeter FEK-56M or spectrophotometer SF-4, or other similar devices.

Glass cylinders with a capacity of 250 ml made of transparent colorless glass (internal diameter 36-40 mm) in accordance with GOST 1770-74.

Water bath.

Sodium hydroxide (sodium hydroxide) according to GOST 4328-77, 3% solution.

Tannin, 2% solution in 1% ethanol.

(Changed edition, Amendment No. 2).

6.3. Preparing for the test

From an analytical sample of sand in a state of natural moisture, take a sample of about 250 g.

Prepare a standard solution by dissolving 2.5 ml of a 2% tannin solution in 97.5 ml of a 3% sodium hydroxide solution. The prepared solution is stirred and left for 24 hours.

The optical density of the tannin solution, determined on a photocolorimeter or spectrophotometer in the wavelength region of 450-500 nm, should be 0.60-0.68.

6.4. Carrying out the test

Sand is suitable for use in concrete or mortars if the liquid above the sample is colorless or is significantly less colored than the reference solution.

If the color of the liquid is the same or darker than the color of the reference solution, it is necessary to test the aggregate in concrete or solutions in specialized laboratories.

7. DETERMINATION OF MINERALOGICAL-PETROGRAPHIC COMPOSITION

7.1. Essence of the method

Set of sieves with mesh No. 1.25; 063; 0315 and 016 according to GOST 6613-86 and with round holes with diameters of 5 and 2.5 mm.

Drying cabinet.

Binocular microscope with magnification from 10 to 50C, polarizing microscope with magnification up to 1350C.

Mineralogical magnifying glass according to GOST 25706-83.

Set of reagents.

Steel needle.

(Changed edition, Amendment No. 2).

7.3. Preparing for the test

An analytical sand sample is sifted through a sieve with holes 5 mm in diameter, and at least 500 g of sand is taken from the sifted part of the sample.

The sand is washed, dried to a constant weight, scattered on a set of sieves with holes with a diameter of 2.5 mm and mesh No. 1.25; 063; 0315; 016 and select samples weighing at least:

25.0 g - for sand with a grain size of St. 2.5 to 5.0 mm;

5.0 g » » » » » St. 1.25 to 2.5 mm;

1.0 g » » » » » St. 0.63 to 1.25 mm;

0.1 g » » » » » St. 0.315 to 0.63 mm;

0.01 g » » » » » from 0.16 to 0.315 mm.

7.4. Carrying out the test

Each sample is poured in a thin layer onto glass or paper and viewed using a binocular microscope or magnifying glass.

Sand grains, represented by fragments of the corresponding rocks and minerals, are separated using a thin needle into groups according to rock types and types of minerals.

In sand grains, represented by mineral fragments, the content of quartz, feldspar, dark-colored minerals, calcite, etc. is determined.

Sand grains, represented by rock fragments, are divided into genetic types in accordance with Table. .

table 2

In addition, grains of rocks and minerals classified as harmful impurities are isolated in the sand.

The same samples of sand are used to determine the shape and nature of the surface of sand grains in accordance with Table. .

Table 3

7.5. Processing the results

For each type of isolated rocks and minerals, the number of grains is counted and their content is determined ( X) as a percentage in a sample according to the formula

Where n - the number of grains of a given rock or mineral;

N- the total number of grains in the test sample.

8. DETERMINATION OF TRUE DENSITY

8.1. Pycnometric method

8.1.1. Essence of the method

True density is determined by measuring the mass per unit volume of dried sand grains.

Piconometer with a capacity of 100 ml according to GOST 22524-77.

Desiccator according to GOST 25336-82.

Drying cabinet.

Sand bath or water bath.

GOST 450-77.

(Changed edition, Amendment No. 2).

8.1.3. Preparing for the test

8.1.4. Carrying out the test

8.1.5. Processing the results

Where T - mass of pycnometer with sand, g;

T 1 - mass of empty pycnometer, g;

T 2 - mass of pycnometer with distilled water, g;

T 3 - mass of the pycnometer with sand and distilled water after removing air bubbles, g;

rв is the density of water equal to 1 g/cm3.

The discrepancy between the results of two determinations of true density should not be more than 0.02 g/cm3. In cases of large discrepancies, a third determination is carried out and the arithmetic mean of the two closest values is calculated.

Notes:

1. When testing sand consisting of grains of porous sedimentary rocks using this method, they are first crushed in a cast iron or porcelain mortar to a particle size of less than 0.16 mm and then determined in the sequence described above.

2. Instead of weighing the pycnometer with distilled water during each test, it is allowed to determine the capacity of the pycnometer once and use its value for all tests. In this case, the determination of the capacity of the pycnometer and all tests are carried out at a steady temperature (20±1)°C. The capacity of the pycnometer is determined by the mass of distilled water in the pycnometer, the density of which is taken to be 1.0 g/cm3. In this case, the true density of sand is calculated using the formula

(16)

Where V- pycnometer volume, ml.

The remaining notations are based on the formula ().

8.2. Accelerated True Density Determination

8.2.1. Essence of the method

True density is determined by measuring the mass per unit volume of dried sand grains using a Le Chatelier apparatus.

Weighing glass or porcelain cup according to GOST 9147-80.

Desiccator according to GOST 25336-82.

Drying cabinet.

Sieve with round holes 5 mm.

Sulfuric acid according to GOST 2184-77.

Calcium chloride (calcium chloride) according to GOST 450-77.

(Changed edition, Amendment No. 2).

8.2.3. Preparing for the test

About 200 g of sand is taken from the analytical sample, sifted through a sieve with holes 5 mm in diameter, poured into a weighing glass or porcelain cup, dried to a constant weight and cooled to room temperature in a desiccator over concentrated sulfuric acid or anhydrous calcium chloride. After this, two samples weighing 75 g each are weighed.

8.2.4. Carrying out the test

The device is filled with water to the lower zero line, and the water level is determined by the lower meniscus. Each sample of sand is poured through the funnel of the device in small uniform portions until the liquid level in the device, determined by the lower meniscus, rises to a mark with a division of 20 ml (or another division within the upper graduated part of the device).

To remove air bubbles, the device is rotated several times around its vertical axis.

The remainder of the sand that is not included in the device is weighed, all weighings are carried out with an error of up to 0.01 g.

8.2.5. Processing the results

The true density of sand (r) in g/cm3 is calculated using the formula

Where T - weight of a sample of sand, g;

T 1 - mass of sand residue, g;

V- volume of water displaced by sand, ml.

The discrepancy between the results of two determinations of true density should not be more than 0.02 g/cm3. In cases of large discrepancies, a third determination is made and the arithmetic mean of the two closest values is calculated.

9. DETERMINATION OF BULK DENSITY AND VOIDITY

9.1. Determination of bulk density

9.1.1. Essence of the method

Bulk density is determined by weighing sand in measuring vessels.

A sieve with round holes with a diameter of 5 mm.

(Changed edition, Amendment No. 2).

9.1.3. Preparing for the test

9.1.3.1. When determining bulk density in a standard uncompacted state during incoming inspection, tests are carried out in a measuring cylindrical vessel with a capacity of 1 liter, using about 5 kg of sand, dried to a constant weight and sifted through a sieve with round holes with a diameter of 5 mm.

9.1.4. Carrying out the test

The bulk density of sand (rn) in kg/m3 is calculated using the formula

Where T - mass of the measuring vessel, kg;

T 1 - mass of a measuring vessel with sand, kg;

V- volume of the vessel, m3.

Determination of the bulk density of sand is carried out twice, each time taking a new portion of sand.

Note. The bulk density of the sand-gravel mixture is determined according to GOST 8269-87.

9.2. Definition of voidness

The voidness (volume of intergranular voids) of sand in a standard uncompacted state is determined based on the values of the true density and bulk density of sand, previously established according to paragraphs. And .

Emptiness of sand ( V m.p) as a percentage by volume is calculated using the formula

(19)

Where r- true density of sand, g/cm3;

r n - bulk density of sand, kg/m3.

10. DETERMINATION OF HUMIDITY

10.1. Essence of the method

Humidity is determined by comparing the mass of sand in a state of natural humidity and after drying.

Drying cabinet.

Baking tray.

(Changed edition, Amendment No. 2).

10.3. Carrying out the test

A sample weighing 1000 g of sand is poured into a baking sheet and immediately weighed, and then dried in the same baking sheet to a constant weight.

10.4. Processing the results

Sand moisture ( W) as a percentage is calculated using the formula

(20)

Where T - weight of the sample in a state of natural humidity;

T 1 - weight of the sample in dry condition, g.

11. DETERMINATION OF REACTIVITY

The test is carried out in accordance with GOST 8269-87, using a sample of sand weighing at least 250 g.

12. DETERMINATION OF THE CONTENT OF SULPHATE AND SULPHIDE COMPOUNDS

If only sulfate compounds are present in the sand, the total sulfur content is not determined.

12.2. Determination of total sulfur content

12.2.1. Weight method

12.2.1.1. Essence of the method

The gravimetric method is based on the decomposition of a sample with a mixture of nitric and hydrochloric acids, followed by the precipitation of sulfur in the form of barium sulfate and determination of the mass of the latter.

The furnace is a muffle furnace, providing a heating temperature of 900 °C.

Porcelain cups with a diameter of 15 cm according to GOST 9147-80.

Glass glasses with a capacity of 100, 200 300 400 ml according to GOST 23932-90.

Porcelain crucibles according to GOST 9147-80.

Desiccator according to GOST 25336-82.

Water bath.

Calcium chloride (calcium chloride) according to GOST 450-77, calcined at a temperature of 700-800 °C.

Ash paper filters according to TU 6-09-1706-82.

Nitric acid according to GOST 4461-77.

Hydrochloric acid according to GOST 3118-77.

Aqueous ammonia according to GOST 3760-79, 10% solution.

Barium chloride (barium chloride) according to GOST 4108-72, 10% solution.

Methyl orange according to TU 6-09-5169-84, 0.1% solution.

Silver nitrate (silver nitrate) according to GOST 1277-75, 1% solution.

Wire woven sieves with square cells No. 005 and 0071 according to GOST 6613-86.

(Changed edition, Amendment No. 2).

The crushed sand is dried to a constant weight, placed in a bottle, stored in a desiccator over calcined calcium chloride, and samples are taken from it for analysis ( T) weighing 0.5-2 g.

The sample, weighed with an accuracy of 0.0002 g, is placed in a glass beaker with a capacity of 200 ml or a porcelain cup, moistened with a few drops of distilled water, 30 ml of nitric acid is added, covered with glass and left for 10-15 minutes. After the reaction is complete, add 10 ml of hydrochloric acid, stir with a glass rod, cover with glass and place the glass or cup in a water bath. 20-30 minutes after the release of brown vapors of nitrogen oxides ceases, the glass is removed and the contents of the glass or cup are evaporated to dryness. After cooling, the residue is moistened with 5-7 ml of hydrochloric acid and again evaporated to dryness. The operation is repeated 2-3 times, add 50 ml of hot water and boil until the salts are completely dissolved.

To precipitate elements of the sesquioxide group, add 2-3 drops of methyl orange indicator to the solution and add ammonia solution until the color of the solution changes from red to yellow and the smell of ammonia appears. After 10 minutes, the coagulated sesquioxide precipitate is filtered through a “red ribbon” filter into a glass with a capacity of 300-400 ml. The precipitate is washed with warm water with the addition of a few drops of ammonia solution. Hydrochloric acid is added to the filtrate until the color of the solution turns pink and another 2.5 ml of acid is added.

The filtrate is diluted with water to a volume of 200-250 ml, heated to a boil, 10 ml of a hot barium chloride solution is poured into it at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense filter " blue tape" and washed 10 times with small portions of cold water until the chloride ions are removed.

Note. The expression “blind experiment” means that the test is carried out in the absence of the test object, using the same reagents and observing all experimental conditions.

Where T - sample weight, g;

T 1 - mass of barium sulfate sediment, g;

T 2 - mass of barium sulfate sediment in the “dead experiment”, g;

0.343 - conversion factor of barium sulfate to SO3.

Acceptable differences between the results of two parallel analyzes with a confidence level R= 0.95 should not exceed the values indicated in the table. . Otherwise, the analysis should be repeated until an acceptable difference is obtained.

Table 4

	Permissible discrepancy, abs. %

St. 0.5 to 1.0

12.2.2. Iodometric titration method

12.2.2.1. Essence of the method

The method is based on burning a sample in a flow of carbon dioxide at a temperature of 1300-1350 °C, absorbing the released SO2 with an iodine solution and titrating with a sodium thiosulfate solution the excess iodine that has not reacted with the resulting sulfurous acid.

Sodium thiosulfate according to GOST 27068-86, 0.005 n. solution.

Sodium carbonate (sodium carbonate) according to GOST 83-79.

Potassium dichromate (potassium dichromate) according to GOST 4220-75, fixanal.

Soluble starch according to GOST 10163-76, 1.0% solution.

Iodine according to GOST 4159-79, 0.005 N solution.

Potassium iodide (potassium iodide) according to GOST 4232-74.

Sulfuric acid according to GOST 4204-77, 0.1 N solution.

Analytical balance, measurement error 0.0002 g.

To prepare a solution of sodium thiosulfate, dissolve 1.25 g of Na2S2O3 5 H2O in 1 liter of freshly boiled distilled water and add 0.1 g of sodium carbonate. The solution is stirred and left for 10-12 days, after which its titer is determined using a 0.01 N solution of potassium dichromate prepared from fixanal.

To 10 ml of a 0.01 N solution of potassium dichromate, add 50 ml of a 0.1 N solution of sulfuric acid, 2 g of dry potassium iodide and titrate with the prepared sodium thiosulfate solution until the color is straw-yellow. Add a few drops of 1% starch solution (the solution turns blue) and titrate until the solution becomes discolored. The correction factor for the titer of a 0.005 N sodium thiosulfate solution is determined by the formula

(22)

where is the normality of the potassium dichromate solution;

10 - volume of 0.01 N solution of potassium bichromate taken for titration, ml;

V- volume of 0.005 N sodium thiosulfate solution used for titration of 10 ml of 0.01 N solution of potassium dichromate, ml;

Normality of sodium thiosulfate solution.

The titer is checked at least once every 10 days.

The sodium thiosulfate solution is stored in dark bottles.

The titer of the prepared iodine solution is determined using a titrated solution of sodium thiosulfate prepared in the manner described above (p.).

10 ml of 0.005 N iodine solution is titrated with 0.005 N sodium thiosulfate solution in the presence of starch.

The correction factor for the titer of 0.005 N iodine solution () is determined by the formula

(23)

where is the volume of 0.005 N sodium thiosulfate solution used for titrating the iodine solution, ml;

Correction factor 0.005 N sodium thiosulfate solution;

- normality of iodine solution;

10 - amount of iodine solution taken for titration, ml.

12.2.2.5. Preparing for the test

Samples for testing are prepared according to clause 12.1.1.3, with the weight of the samples taken equal to 0.1-1.0 g.

12.2.2.6. Testing

Installation diagram for determining sulfur content

1 - carbon dioxide cylinder; 2 - washing bottle with a 5% solution of copper sulfate; 3 - washing bottle with a 5% solution of potassium permanganate; 4 - block with calcined calcium chloride; 5 - rubber plugs; 6 - electric tube furnace with silit rods, providing a heating temperature of 1300 °C; 7 - porcelain tube for calcination 70-75 mm long, internal diameter 18-20 mm; 8 - porcelain boat No. 1 (length 70, width 9, height 7-5 mm) or porcelain boat No. 2 (length 95, width 12, height 10 mm) according to GOST 9147-80; 9 - tap; 10 - absorption vessel; II - burette with iodine solution; I2 - burette with sodium thiosulfate solution

Note. All parts of the installation are connected end-to-end by rubber tubes. To prevent burning of rubber plugs, the inner end surface is covered with asbestos gaskets.

A boat with a hinge is placed in a heated tube (from the carbon dioxide supply side) using a hook made of heat-resistant wire. Close the tube with a stopper and supply carbon dioxide (speed 90-100 bubbles per 1 min). The sample is calcined for 10-15 minutes, making sure that the solution in the absorption vessel retains its blue color. The solution in the absorption vessel is then titrated with sodium thiosulfate solution until colorless. After the titration is complete, remove the boat from the oven, being careful not to contaminate the walls of the porcelain tube with sample residues.

A new portion of water, a solution of iodine and starch is poured into the absorption vessel, washed with water.

12.2.2.7. Processing the results

(24)

Where V- volume of iodine solution taken for titration, ml;

V 1 - volume of sodium thiosulfate solution consumed for titration of excess iodine that did not react, ml;

TO - coefficient of ratio between the concentrations of iodine solution and sodium thiosulfate;

2.5 - conversion factor of sulfur to SO3;

T - mass of sample sample, g;

Titer of 0.005 N iodine solution for sulfur, g/ml, determined by the formula

where 0.1263 is the conversion factor for the mass of iodine to the equivalent mass of sulfur;

Titer of 0.005 N iodine solution over sodium thiosulfate solution, g/ml, determined by the formula

(26)

where is the correction factor of 0.005 N sodium thiosulfate solution;

Normality of sodium thiosulfate solution;

A - volume of 0.005 N sodium thiosulfate solution used for titrating the iodine solution, ml;

126.92 - 1 g-equiv of iodine, g;

10 - volume of 0.005 N iodine solution taken for titration, ml;

1000 - volume of sodium thiosulfate solution, ml.

Acceptable discrepancies between the results of two parallel determinations with a confidence level R= 0.95 should not exceed the values indicated in the table. . Otherwise, the experiment should be repeated until an acceptable discrepancy is obtained.

12.3. Determination of sulfate sulfur content

12.3.1. Essence of the method

The method is based on the decomposition of a sample with hydrochloric acid, followed by the precipitation of sulfur in the form of barium sulfate and determination of the mass of the latter.

12.3.3. Preparing for the test

The sample for testing is prepared according to clause 12.1.1.3, with the mass of the sample being taken equal to 1 g.

12.3.4. Testing

The filtrate is neutralized with hydrochloric acid until the color of the solution turns pink and another 2.5 ml of acid is added. The solution is heated to a boil and 10 ml of a hot barium chloride solution is added at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense blue ribbon filter and washed 10 times with small portions of cold water until chloride ions are removed.

After cooling in the desiccator, the crucible with the sediment is weighed. Calcination is repeated until a constant mass is obtained.

Acceptable discrepancies between the results of two parallel analyzes are accepted according to clause.

12.4. Determination of sulfide sulfur content

Where X - total sulfur content in terms of SO3, %;

X 1 - content of sulfate sulfur in terms of SO3, %.

13. DETERMINATION OF FROST RESISTANCE OF SAND FROM CRUSHING SEEDS

13.1. Essence of the method

The frost resistance of sand is determined by the loss of mass during successive freezing and thawing.

Freezer chamber.

Sieves with mesh No. 1.25; 016 according to GOST 6613-86 and with round holes with a diameter of 5 mm.

Vessel for thawing samples.

Fabric bags made of thick fabric with double walls.

Baking trays.

(Changed edition, Amendment No. 2).

13.3.Sample preparation

13.4.Testing

Each sample is placed in a bag that ensures the safety of the grains, immersed in a vessel with water to saturate for 48 hours. The bag with the sample is removed from the water and placed in a freezer, which ensures a gradual decrease in temperature to minus (20±5) °C.

After the required number of freezing and thawing cycles, the sample from the bag is poured onto a control sieve with mesh No. 1.25 or 016, carefully washing off the remaining grains from the walls of the bag. The sample placed on the control sieve is washed, and the residue is dried to a constant weight.

GOST 8735-88

(ST SEV 5446 ¾ 85)

ST SEV 6317 ¾ 88

UDC 691.223.001.4.006.354 Group Zh19

STATE STANDARD OF THE USSR UNION

SAND FOR CONSTRUCTION WORK
Test methods

Sand for construction work.

Testing methods

OKSTU 5711

Date of introduction 01.07.89

Failure to comply with the standard is punishable by law

1. GENERAL PROVISIONS

1.1. The scope of application of the sand testing methods provided for in this standard is specified in the appendix.

1.2. Samples are weighed with an error of 0.1% by weight, unless otherwise specified in the standard.

1.3. Samples or weighed portions of sand are dried to constant weight in an oven at a temperature of (105 ± 5) ° Until the difference between the results of two weighings is no more than 0.1% of the mass. Each subsequent weighing is carried out after drying for at least 1 hour and cooling for at least 45 minutes.

1.4. Test results are calculated to the second decimal place unless otherwise specified regarding the accuracy of the calculation.

1.5. The arithmetic mean of the parallel determinations provided for the corresponding method is taken as the test result.

1.6. A standard set of sieves for sand includes sieves with round holes with diameters of 10; 5 and 2.5 mm and wire sieves with standard square cells No. 1.25; 063; 0315; 016; 005 according to GOST 6613 (sieve frames are round or square with a diameter or side side of at least 100 mm).

Note. The use of sieves with meshes No. 014 is allowed before equipping enterprises with sieves with meshes No. 016.

1.7. The temperature of the room in which the tests are carried out must be (25 ± 10) °C. Before starting the test, the sand and water must be at a temperature corresponding to the air temperature in the room.

1.8. Water for testing is used in accordance with GOST 2874 or GOST 23732, if the standard does not provide instructions on the use of distilled water.

1.9. When using hazardous (caustic, toxic) substances as reagents, one should follow safety requirements, set out in the regulatory and technical documents for these reagents.

1.10. The “Equipment” sections provide links to state standards. The use of similar imported equipment is permitted. The non-standard measuring instruments used, specified in the “Equipment” section, must undergo metrological certification in accordance with GOST 8.326.

2. SAMPLING

2.1. During acceptance control at the manufacturing plant, spot samples are taken, from which, by mixing, one combined sample is obtained from the replacement products of each production line.

To check the quality of sand shipped directly at the quarry face, spot samples are taken during loading into vehicles.

2.3. Point samples to obtain a pooled sample begin to be taken 1 hour after the start of the shift and then taken every hour during the shift.

Depending on the obtained maximum value of the coefficient of variation for the two indicators being determined, the following intervals for taking point samples during the shift are taken:

3 hours - with a coefficient of variation of the indicator up to 10%;

2 hours ” ” ” ” ” 15%.

2.4. The mass of a spot sample at a sampling interval of 1 hour must be at least 1500 g. When increasing the sampling interval in accordance with clause 2.3, the mass of the selected spot sample must be increased at an interval of 2 hours - twice, at an interval of 3 hours - four times.

2.5. The combined sample is mixed and reduced by quartering or a trough divider to obtain a laboratory sample before being sent to the laboratory.

2.6. The mass of the laboratory sample during acceptance control at the manufacturer must be at least 5000 g; it is used for all tests provided for during acceptance control.

2.7. For each test, an analytical sample is taken from the laboratory sample.

Samples are taken from the analytical sample in accordance with the test procedure.

The selected samples are packaged in such a way that the mass and properties of the materials do not change before testing.

Each sample is provided with two labels indicating the sample designation. One label is placed inside the package, the other is placed in a visible place on the package.

During transportation, the packaging must be protected from mechanical damage and wetness.

2.9. To check the quality of sand extracted and laid by hydromechanization, the alluvium map is divided in plan along the length (along the alluvium map) into three parts.

From spot samples, a combined sample is obtained by mixing, which is reduced to obtain a laboratory sample according to clause 2.5.

The quality of sand is assessed separately for each part of the alluvium map based on the results of testing a sample taken from it.

2.11. During incoming inspection at the consumer enterprise, a combined sand sample is taken from the tested batch of material in accordance with the requirements of GOST 8736. A laboratory sample is prepared according to clause 2.5.

2.12. During geological exploration, samples are taken in accordance with regulatory and technical documentation approved in the prescribed manner.

3. DETERMINATION OF GRAIN COMPOSITION AND FINANCY MODULE

3.1. Essence of the method

The grain composition is determined by sifting sand on a standard set of sieves.

3.2. Equipment

A set of sieves in accordance with GOST 6613 and sieves with round holes with a diameter of 10; 5 and 2.5 mm.

Drying cabinet.

3.3. Preparing for the test

An analytical sample of sand weighing at least 2000 g is dried to a constant weight.

3.4. Carrying out the test

A sand sample dried to constant weight is sifted through sieves with round holes with diameters of 10 and 5 mm.

The residues on the sieves are weighed and the content of gravel fractions in the sand with a grain size of 5 to 10 mm is calculated ( Gr 5) and St. 10 mm ( Gr 10) in percent by weight according to the formulas:

(1)

(2)

Where M 10 - residue on a sieve with round holes with a diameter of 10 mm, g;

M 5 - residue on a sieve with round holes with a diameter of 5 mm, g;

M - sample weight, g.

From a portion of the sand sample that has passed through a sieve with holes 5 mm in diameter, a sample weighing at least 1000 g is taken to determine the grain composition of the sand.

During geological exploration, it is allowed to disperse the sample after preliminary washing to determine the content of dust and clay particles. When calculating the sieving results, the content of dust and clay particles is included in the mass of particles passing through a sieve with mesh No. 016 and in the total mass of the sample. During mass testing, it is allowed, after washing to determine the content of dust and clay particles and drying the sample to a constant weight, to sift a sample of sand (without the gravel fraction) weighing 500 g.

The prepared sample of sand is sifted through a set of sieves with round holes with a diameter of 2.5 mm and mesh No. 1.25; 063; 0315 and 016.

Sifting is carried out mechanically or manually. The duration of sifting should be such that during control intensive manual shaking of each sieve for 1 minute, no more than 0.1% of the total mass of the sifted sample passes through it. During mechanical sifting, its duration for the device used is determined experimentally.

When sifting by hand, it is possible to determine the end of sifting by vigorously shaking each sieve over a sheet of paper. Sifting is considered complete if practically no falling of sand grains is observed.

When determining grain composition wet method a sample of the material is placed in a vessel and filled with water. After 24 hours, the contents of the vessel are thoroughly mixed until the clay film is completely soaked into grains or lumps of clay, poured (in portions) onto the upper sieve standard set and sift, washing the material on sieves until the wash water becomes clear. The partial residues on each sieve are dried to constant weight and cooled to room temperature, then their weight is determined by weighing.

(Changed edition, Amendment No. 1).

3.5. Processing the results

Based on the sifting results, calculate:

Partial residue on each sieve ( A i) as a percentage according to the formula

(3)

Where t i - mass of residue on this sieve, g;

T - weight of the sample being sifted, g;

Total residue on each sieve ( A i) as a percentage according to the formula

(4)

Where a 2,5 , a 1,25 , a i - partial residues on the corresponding sieves;

Sand fineness modulus ( M j) without grains larger than 5 mm according to the formula

(5)

Where A 2,5 , A 1,25 ,A 063 , A 0315 , A 016 - complete residues on a sieve with round holes with a diameter of 2.5 mm and on sieves with mesh No. 1.25; 063; 0315, 016, %.

The result of determining the grain composition of sand is drawn up in accordance with table. 1 or depicted graphically in the form of a sifting curve in accordance with Fig. 1.

Screening curve

Crap. 1

Table 1

	Residues, % by weight, on sieves					Passage through
Name of balance		1,25	0,63	0,315	0,16 (0,14)	Sieve with mesh № 016(014), % by weight
Private	A 2,5	A 1,25	A 063	A 0315	A 016(014)	A 016(014)
Full	A 2,5	A 1,25	A 063	A 0315	A 016(014)

4. DETERMINATION OF CLAY CONTENT IN Lumps

4.1. Essence of the method

4.2. Equipment

Scales according to GOST 23711 or GOST 24104.

Drying cabinet.

Sieves with mesh No. 1.25 according to GOST 6613 and with round holes with diameters of 5 and 2.5 mm.

Steel needle.

4.3. Preparing for the test

5.0 g - fractions of St. 2.5 to 5 mm;

1.0 g - fractions from 1.25 to 2.5 mm

Each sample of sand is poured into a thin layer onto glass or a metal sheet and moistened using a pipette. Using a steel needle, lumps of clay are separated from the sample, which differ in viscosity from sand grains, using a magnifying glass if necessary. The sand grains remaining after separating the lumps are dried to a constant mass and weighed.

4.4. Processing the results

(6)

(7)

Where m 1 , m 2 - weight of a sample of sand fraction, respectively, from 2.5 to 5 mm and from 1.25 to 2.5 mm before the release of clay, g;

T 1, m 3 - mass of grains of sand fractions respectively from 2.5 to 5 mm and from 1.25 to 2.5 mm after the release of clay, g.

(8)

Where A 2,5 , A 1.25 - partial residues as a percentage by weight on sieves with openings of 2.5 and 1.25 mm, calculated according to clause 3.5.

5. DETERMINATION OF THE CONTENT OF DUST AND CLAY PARTICLES

5.1. Elutriation method

5.1.1. Essence of the method

5.1.2. Equipment

Scales according to GOST 23711 or GOST 24104.

Drying cabinet.

A cylindrical bucket with a height of at least 300 mm with a siphon or a vessel for removing sand (Fig. 2).

Stopwatch.

5.1.3. Preparing for the test

5.1.4. Carrying out the test

After elutriation, the washed sample is dried to constant weight. T 1 .

5.1.5. Processing the results

(9)

Where T - mass of the dried sample before elutriation, g;

m1 - mass of the dried sample after elutriation, g.

Vessel for elutriation

Crap. 2

Notes:

1. When testing natural sands, the grains of which are tightly cemented with clay, the sample is kept in water for at least 1 day.

(10)

Where T c is the mass of the sample in a state of natural humidity, g;

T 1 - mass of sample dried after elutriation to constant mass, g;

W- moisture content of the tested sand, %.

5.2. Pipette method

5.2.1. Essence of the method

5.2.2. Equipment

The bucket is cylindrical with two marks (belts) on the inner wall, corresponding to a capacity of 5 and 10 liters.

The bucket is cylindrical without marks.

Drying cabinet.

Sieves with mesh No. 063 and 016 according to GOST 6613.

Metal cylinders with a capacity of 1000 ml with an observation window (2 pcs.).

Metal measuring pipette with a capacity of 50 ml (Fig. 3).

Funnel with a diameter of 150 mm.

Stopwatch.

Cup or glass for evaporation according to GOST 9147.

5.2.3. Carrying out the test

The suspension in each cylinder is stirred with a glass or metal rod or the cylinder is tilted several times, closing it with a lid, for better mixing.

Metal cylinder and measuring pipette

1 - cylinder; 2 - pipette; 3 - label (1000 ml);

4 - suspension level in the cylinder

Crap. 3

5.2.4. Processing the results

(11)

Where T - weight of a sample of sand, g;

T 1 - mass of a cup or glass for evaporating the suspension, g;

T 2 - weight of a cup or glass with evaporated powder, g.

(12)

Note. Allowed mass of sediment ( T 2 -T 1) determined by the density of the suspension using the formula

(13)

Where T 3 - mass of pycnometer with suspension, g;

T 4 - mass of pycnometer with water, g;

r - sediment density, g/cm 3 (assumed equal to 2.65 g/cm 3).

The result of determining the mass of sediment T 2 -T 1 is included in formula (11).

5.3. Wet sieving method

5.3.1. Essence of the method

The test is carried out in accordance with GOST 8269, using a sample of sand weighing 1000 g and sieves with mesh No. 0315 and 005.

5.4. Photoelectric method

5.4.1. Essence of the method

The method is based on comparing the degree of transparency of pure water and the suspension obtained by washing sand.

The test is carried out according to GOST 8269, using a sample of sand weighing 1000 g.

6. DETERMINATION OF THE PRESENCE OF ORGANIC IMPURITIES

6.1. Essence of the method

The presence of organic impurities (humic substances) is determined by comparing the color of the alkaline solution over the sand sample with the color of the standard.

6.2. Equipment, reagents and solutions

Scales according to GOST 29329 or GOST 24104.

Photocolorimeter FEK-56M or spectrophotometer SF-4, or other similar devices.

Glass cylinders with a capacity of 250 ml made of transparent colorless glass (internal diameter 36-40 mm) according to GOST 1770.

Water bath.

Sodium hydroxide (sodium hydroxide) according to GOST 4328, 3% solution.

Tannin, 2% solution in 1% ethanol.

6.3. Preparing for the test

From an analytical sample of sand in a state of natural moisture, take a sample of about 250 g.

Prepare a standard solution by dissolving 2.5 ml of a 2% tannin solution in 97.5 ml of a 3% sodium hydroxide solution. The prepared solution is stirred and left for 24 hours.

The optical density of the tannin solution, determined on a photocolorimeter or spectrophotometer in the wavelength region of 450-500 nm, should be 0.60-0.68.

6.4. Carrying out the test

Sand is suitable for use in concrete or mortars if the liquid above the sample is colorless or is significantly less colored than the reference solution.

If the color of the liquid is the same or darker than the color of the reference solution, it is necessary to test the aggregate in concrete or solutions in specialized laboratories.

7. DETERMINATION OF MINERALOGICAL-PETROGRAPHIC COMPOSITION

7.1. Essence of the method

7.2. Equipment and reagents

Scales according to GOST 29329 or GOST 24104.

Set of sieves with mesh No. 1.25; 063; 0315 and 016 according to GOST 6613 and with round holes with diameters of 5 and 2.5 mm.

Drying cabinet.

Binocular microscope with magnification from 10 to 50 C , polarizing microscope with magnification up to 1350 C.

Mineralogical magnifying glass according to GOST 25706.

Set of reagents.

Steel needle.

7.3. Preparing for the test

An analytical sand sample is sifted through a sieve with holes 5 mm in diameter, and at least 500 g of sand is taken from the sifted part of the sample.

The sand is washed, dried to a constant weight, scattered on a set of sieves with holes with a diameter of 2.5 mm and mesh No. 1.25; 063; 0315; 016 and select samples weighing at least:

25.0 g - for sand with a grain size of St. 2.5 to 5.0 mm;

5.0 g ” ” ” ” ” St. 1.25 to 2.5 mm;

1.0 g ” ” ” ” ” St. 0.63 to 1.25 mm;

0.1 g ” ” ” ” ” St. 0.315 to 0.63 mm;

0.01 g ” ” ” ” ” from 0.16 to 0.315 mm.

7.4. Carrying out the test

Each sample is poured in a thin layer onto glass or paper and viewed using a binocular microscope or magnifying glass.

Sand grains, represented by fragments of the corresponding rocks and minerals, are separated using a thin needle into groups according to rock types and types of minerals.

In sand grains, represented by mineral fragments, the content of quartz, feldspar, dark-colored minerals, calcite, etc. is determined.

Sand grains, represented by rock fragments, are divided into genetic types in accordance with Table. 2.

table 2

Genetic type of breeds	Breed
Sedimentary	Limestone, dolomite, sandstone, flint, etc.
Erupted: Intrusive	Granite, gabbro, diorite, etc.
Effusive	Basalt, porphyrite, diabase, etc.
Metamorphic	Quartzite, crystalline schists, etc.

In addition, grains of rocks and minerals classified as harmful impurities are isolated in the sand.

In the presence of minerals containing sulfur, the amount of sulfate and sulfide compounds in terms of SO 3 is determined according to clause 12.

Quantitative determination of the content of potentially reactive species of silica is carried out according to paragraph 11.

The same samples of sand are used to determine the shape and nature of the surface of sand grains in accordance with Table. 3.

Table 3

7.5. Processing the results

For each type of isolated rocks and minerals, the number of grains is counted and their content is determined ( X) as a percentage in a sample according to the formula

(14)

Where n-the number of grains of a given rock or mineral;

N- the total number of grains in the test sample.

8. DETERMINATION OF TRUE DENSITY

8.1. Pycnometric method

8.1.1. Essence of the method

True density is determined by measuring the mass per unit volume of dried sand grains.

8.1.2. Equipment

Piconometer with a capacity of 100 ml according to GOST 22524.

Scales according to GOST 29329 or GOST 24104.

Desiccator according to GOST 25336.

Drying cabinet.

Sand bath or water bath.

Distilled water according to GOST 6709.

8.1.3. Preparing for the test

8.1.4. Carrying out the test

8.1.5. Processing the results

The true density of sand ( r

(15)

Where T - mass of pycnometer with sand, g;

T 1 - mass of empty pycnometer, g;

T 2 - mass of pycnometer with distilled water, g;

T 3 - mass of the pycnometer with sand and distilled water after removing air bubbles, g;

r c is the density of water equal to 1 g/cm3.

The discrepancy between the results of two determinations of true density should not be more than 0.02 g/cm 3 . In cases of large discrepancies, a third determination is carried out and the arithmetic mean of the two closest values is calculated.

Notes:

2. Instead of weighing the pycnometer with distilled water during each test, it is allowed to determine the capacity of the pycnometer once and use its value for all tests. In this case, the determination of the capacity of the pycnometer and all tests are carried out at a steady temperature (20±1)°C. The capacity of the pycnometer is determined by the mass of distilled water in the pycnometer, the density of which is taken to be 1.0 g/cm 3 . In this case, the true density of sand is calculated using the formula

(16)

Where V- pycnometer volume, ml.

The remaining designations are according to formula (15).

8.2. Accelerated True Density Determination

8.2.1. Essence of the method

True density is determined by measuring the mass per unit volume of dried sand grains using a Le Chatelier apparatus.

8.2.2. Equipment

Le Chatelier device (Fig. 4).

Scales according to GOST 29329 or GOST 24104.

Weighing glass or porcelain cup according to GOST 9147.

Desiccator according to GOST 25336.

Drying cabinet.

Sieve with round holes 5 mm.

Sulfuric acid according to GOST 2184.

Calcium chloride (calcium chloride) according to GOST 450.

Le Chatelier device

Crap. 4

8.2.3. Preparing for the test

8.2.4. Carrying out the test

To remove air bubbles, the device is rotated several times around its vertical axis.

The remainder of the sand that is not included in the device is weighed, all weighings are carried out with an error of up to 0.01 g.

8.2.5. Processing the results

The true density of sand ( r ) in g/cm 3 is calculated using the formula

(17)

Where T - weight of a sample of sand, g;

T 1 - mass of sand residue, g;

V- volume of water displaced by sand, ml.

The discrepancy between the results of two determinations of true density should not be more than 0.02 g/cm 3 . In cases of large discrepancies, a third determination is made and the arithmetic mean of the two closest values is calculated.

9. DETERMINATION OF BULK DENSITY AND VOIDITY

9.1. Determination of bulk density

9.1.1. Essence of the method

Bulk density is determined by weighing sand in measuring vessels.

9.1.2. Equipment

Scales in accordance with GOST 29329, GOST 24104 or platform scales.

Measuring cylindrical metal vessels with a capacity of 1 liter (diameter and height 108 mm) and a capacity of 10 liters (diameter and height 234 mm).

Drying cabinet.

Metal ruler according to GOST 427.

A sieve with round holes with a diameter of 5 mm.

9.1.3. Preparing for the test

9.1.3.2. When determining the bulk density of sand in a batch to convert the amount of sand supplied from mass units to volume units during acceptance control, tests are carried out in a measuring cylindrical vessel with a capacity of 10 liters. Sand is tested in a state of natural moisture without sifting through a sieve with holes 5 mm in diameter.

9.1.4. Carrying out the test

9.1.5. Processing the results

Bulk density of sand ( r n) in kg/m 3 calculated by the formula

(18)

Where T - mass of the measuring vessel, kg;

T 1 - mass of a measuring vessel with sand, kg;

V- volume of the vessel, m3.

Determination of the bulk density of sand is carried out twice, each time taking a new portion of sand.

Note. The bulk density of the sand-gravel mixture is determined according to GOST 8269.

9.2. Definition of voidness

Emptiness of sand (Vm.p) as a percentage by volume is calculated using the formula

(19)

Where r - true density of sand, g/cm 3 ;

r n - bulk density of sand, kg/m3.

10. DETERMINATION OF HUMIDITY

10.1. Essence of the method

Humidity is determined by comparing the mass of sand in a state of natural humidity and after drying.

10.2. Equipment

Scales according to GOST 29329 or GOST 24104.

Drying cabinet.

Baking tray.

10.3. Carrying out the test

A sample weighing 1000 g of sand is poured into a baking sheet and immediately weighed, and then dried in the same baking sheet to a constant weight.

10.4. Processing the results

Sand moisture (W) as a percentage is calculated using the formula

(20)

Where T - weight of the sample in a state of natural humidity;

T 1 - weight of the sample in dry condition, g.

11. DETERMINATION OF REACTIVITY

The test is carried out in accordance with GOST 8269, using a sample of sand weighing at least 250 g.

12. DETERMINATION OF THE CONTENT OF SULPHATE AND SULPHIDE COMPOUNDS

If only sulfate compounds are present in the sand, the total sulfur content is not determined.

12.2. Determination of total sulfur content

12.2.1. Weight method

12.2.1.1. Essence of the method

12.2.1.2.

The furnace is a muffle furnace, providing a heating temperature of 900 °C.

Porcelain cups with a diameter of 15 cm according to GOST 9147.

Glass glasses with a capacity of 100, 200 300 400 ml according to GOST 23932.

Porcelain crucibles according to GOST 9147.

Desiccator according to GOST 25336.

Water bath.

Calcium chloride (calcium chloride) according to GOST 450, calcined at a temperature of 700-800 °C.

Ash paper filters according to TU 6-09-1706-82.

Nitric acid according to GOST 4461.

Hydrochloric acid according to GOST 3118.

Aqueous ammonia according to GOST 3760, 10% solution.

Barium chloride (barium chloride) according to GOST 4108, 10% solution.

Methyl orange according to TU 6-09-5169-84, 0.1% solution.

Silver nitrate (silver nitrate) according to GOST 1277, 1% solution.

Wire woven sieves with square cells No. 005 and 0071 according to GOST 6613.

12.2.1.3. Preparing for the test

The crushed sand is dried to a constant weight, placed in a bottle, stored in a desiccator over calcined calcium chloride, and samples are taken from it for analysis ( T) weighing 0.5-2 g.

12.2.1.4. Carrying out analysis

The sample, weighed with an accuracy of 0.0002 g, is placed in a glass beaker with a capacity of 200 ml or a porcelain cup, moistened with a few drops of distilled water, 30 ml of nitric acid is added, covered with glass and left for 10-15 minutes. After the reaction is complete, add 10 ml of hydrochloric acid, stir with a glass rod, cover with glass and place the glass or cup in a water bath. 20-30 minutes after the release of brown vapors of nitrogen oxides ceases, the glass is removed and the contents of the glass or cup are evaporated to dryness. After cooling, the residue is moistened with 5-7 ml of hydrochloric acid and again evaporated to dryness. The operation is repeated 2-3 times, add 50 ml of hot water and boil until the salts are completely dissolved.

To precipitate elements of the sesquioxide group, add 2-3 drops of methyl orange indicator to the solution and add ammonia solution until the color of the solution changes from red to yellow and the smell of ammonia appears. After 10 minutes, the coagulated sesquioxide precipitate is filtered through a “red ribbon” filter into a glass with a capacity of 300-400 ml. The precipitate is washed with warm water with the addition of a few drops of ammonia solution. Hydrochloric acid is added to the filtrate until the color of the solution turns pink and another 2.5 ml of acid is added.

The filtrate is diluted with water to a volume of 200-250 ml, heated to a boil, 10 ml of a hot barium chloride solution is poured into it at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense filter. blue tape” and washed 10 times with small portions of cold water until the chloride ions are removed.

After cooling in the desiccator, the crucible with the sediment is weighed. Calcination is repeated until a constant mass is obtained. To determine the sulfur content in the reagents used for analysis, a “blind experiment” is carried out in parallel with the analysis. The amount of barium sulfate found by “deaf experiment” T 2, subtracted from the mass of barium sulfate T 1 obtained from sample analysis.

Note. The expression “blind experiment” means that the test is carried out in the absence of the test object, using the same reagents and observing all experimental conditions.

12.2.1.5. Processing the results

Total sulfate sulfur content ( X 1) as a percentage based on SO 3 is calculated by the formula

(21)

Where T - sample weight, g;

T 1 - mass of barium sulfate sediment, g;

T 2 - mass of barium sulfate sediment in the “dead experiment”, g;

0.343 - conversion factor of barium sulfate to SO3.

Acceptable differences between the results of two parallel analyzes with a confidence level R= 0.95 should not exceed the values indicated in the table. 4. Otherwise, the analysis should be repeated until an acceptable discrepancy is obtained.

Table 4

	Permissible discrepancy, abs. %
Up to 0.5	0,10
St. 0.5 to 1.0	0,15
” 1,0	0,20

12.2.2. Iodometric titration method

12.2.2.1. Essence of the method

The method is based on burning a sample in a flow of carbon dioxide at a temperature of 1300-1350 °C, absorbing the released SO 2 with a solution of iodine and titration with a solution of sodium thiosulfate of the excess iodine that has not reacted with the resulting sulfurous acid.

12.2.2.2. Equipment, reagents and solutions

Installation for determining sulfur content (Fig. 5).

Sodium thiosulfate according to GOST 27068, 0.005 n. solution.

Sodium carbonate (sodium carbonate) according to GOST 83.

Potassium dichromate (potassium dichromate) according to GOST 4220, fixanal.

Soluble starch according to GOST 10163, 1.0% solution.

Iodine according to GOST 4159, 0.005 N solution.

Potassium iodide (potassium iodide) according to GOST 4232.

Sulfuric acid according to GOST 4204, 0.1 N solution.

Analytical balance, measurement error 0.0002 g.

12.2.2.3. Preparation of 0.005 N sodium thiosulfate solution

To prepare a solution of sodium thiosulfate, dissolve 1.25 g Na 2 S 2 O 3 5 H 2 O in 1 liter of freshly boiled distilled water and add 0.1 g of sodium carbonate. The solution is stirred and left for 10-12 days, after which its titer is determined using a 0.01 N solution of potassium dichromate prepared from fixanal.

To 10 ml of a 0.01 N solution of potassium bichromate, add 50 ml of a 0.1 N solution of sulfuric acid, 2 g of dry potassium iodide and titrate with the prepared sodium thiosulfate solution until the color is straw-yellow. Add a few drops of 1% starch solution (the solution turns blue) and titrate until the solution becomes discolored. Correction factor for the titer of 0.005 N sodium thiosulfate solution determined by the formula

(22)

Where - normality of the potassium dichromate solution;

10 - volume of 0.01 N solution of potassium bichromate, taken for titration, ml;

V- volume of 0.005 N sodium thiosulfate solution used for titration of 10 ml of 0.01 N solution potassium bichromate, ml;

- normality of sodium thiosulfate solution.

The titer is checked at least once every 10 days.

The sodium thiosulfate solution is stored in dark bottles.

12.2.2.4. Preparation of 0.005 N iodine solution

The titer of the prepared iodine solution is determined using a titrated solution of sodium thiosulfate prepared as described above (clause 12.2.2.3).

10 ml of 0.005 N iodine solution is titrated with 0.005 N sodium thiosulfate solution in the presence of starch.

The correction factor for the titer of 0.005 N iodine solution () is determined by the formula

(23)

Where - volume of 0.005 N sodium thiosulfate solution used for titrating the iodine solution, ml;

- correction factor 0.005 N sodium thiosulfate solution;

- normality of iodine solution;

10 - amount of iodine solution taken for titration, ml.

12.2.2.5. Preparing for the test

Samples for testing are prepared according to clause 12.1.1.3, with the weight of the samples taken equal to 0.1-1.0 g.

12.2.2.6. Testing

Installation diagram for determining sulfur content

1 - carbon dioxide cylinder; 2 - wash bottle with 5% solution

Copper sulfate; 3 - washing bottle with a 5% solution of potassium permanganate;

4 - block with calcined calcium chloride; 5 - rubber plugs;

6 - electric tube furnace with silit rods, providing

Heating temperature 1300 °C; 7 - porcelain tube for calcination

Length 70-75 mm, internal diameter 18-20 mm; 8 - porcelain

Boat No. 1 (length 70, width 9, height 7-5 mm) or porcelain

Boat No. 2 (length 95, width 12, height 10 mm) according to GOST 9147;

9 - tap; 10 - absorption vessel; II - burette with iodine solution;

I2 - burette with sodium thiosulfate solution

Crap. 5

Note. All parts of the installation are connected end-to-end by rubber tubes. To prevent burning of rubber plugs, the inner end surface is covered with asbestos gaskets.

A boat with a hinge is placed in a heated tube (from the carbon dioxide supply side) using a hook made of heat-resistant wire. Close the tube with a stopper and supply carbon dioxide (speed 90-100 bubbles per 1 min). The sample is calcined for 10-15 minutes, ensuring that the solution in the absorption vessel retains its blue color. The solution in the absorption vessel is then titrated with sodium thiosulfate solution until colorless. After the titration is complete, remove the boat from the oven, being careful not to contaminate the walls of the porcelain tube with sample residues.

A new portion of water, a solution of iodine and starch is poured into the absorption vessel, washed with water.

12.2.2.7. Processing the results

(24)

Where V- volume of iodine solution taken for titration, ml;

V1 - volume of sodium thiosulfate solution consumed for titration of excess iodine that did not react, ml;

TO - coefficient of ratio between the concentrations of iodine solution and sodium thiosulfate;

A - volume of 0.005 N sodium thiosulfate solution used for titrating the iodine solution, ml;

126.92 - 1 g-equiv of iodine, g;

10 - volume of 0.005 N iodine solution taken for titration, ml;

1000 - volume of sodium thiosulfate solution, ml.

Acceptable discrepancies between the results of two parallel determinations with a confidence level R= 0.95 should not exceed the values indicated in the table. 3. Otherwise, the experiment should be repeated until an acceptable discrepancy is obtained.

12.3. Determination of sulfate sulfur content

12.3.1. Essence of the method

The method is based on the decomposition of a sample with hydrochloric acid, followed by the precipitation of sulfur in the form of barium sulfate and determination of the mass of the latter.

12.3.2. Equipment, reagents and solutions

To carry out the analysis, use the equipment, reagents and solutions specified in clause 12.2.1.2, using hydrochloric acid in accordance with GOST 3118, solution 1:3 (one part by volume of concentrated hydrochloric acid and three parts by volume of water).

12.3.3. Preparing for the test

The sample for testing is prepared according to clause 12.1.1.3, with the mass of the sample being taken equal to 1 g.

12.3.4. Testing

The filtrate is neutralized with hydrochloric acid until the color of the solution turns pink and another 2.5 ml of acid is added. The solution is heated to a boil and 10 ml of a hot barium chloride solution is added at one time, stirred, the solution is boiled for 5-10 minutes and left for at least 2 hours. The precipitate is filtered through a dense “blue ribbon” filter and washed 10 times with small portions of cold water until chloride ions are removed.

After cooling in the desiccator, the crucible with the sediment is weighed. Calcination is repeated until a constant mass is obtained.

In parallel with the analysis, a “deaf experiment” is carried out (see note to clause 12.2.1.4). Barium sulfate quantity T 2, found by “deaf experiment”, is subtracted from the mass of barium sulfate T 1 obtained from sample analysis.

12.3.5. Processing the results

Acceptable discrepancies between the results of two parallel analyzes are accepted according to clause 12.2.1.5.

12.4. Determination of sulfide sulfur content

(27)

Where X - total sulfur content in terms of SO 3,%;

X 1 - content of sulfate sulfur in terms of SO 3,%.

13. DETERMINATION OF FROST RESISTANCE OF SAND FROM CRUSHING SEEDS

13.1. Essence of the method

The frost resistance of sand is determined by the loss of mass during successive freezing and thawing.

13.2. Equipment

Freezer chamber.

Drying cabinet.

Scales according to GOST 29329 or GOST 24104.

Sieves with mesh No. 1.25; 016 according to GOST 6613 and with round holes with a diameter of 5 mm.

Vessel for thawing samples.

Fabric bags made of thick fabric with double walls.

Baking trays.

13.3. Sample preparation

13.4. Testing

Each sample is placed in a bag that ensures the safety of the grains, immersed in a vessel with water to saturate for 48 hours. The bag with the sample is removed from the water and placed in a freezer, which ensures a gradual decrease in temperature to minus (20±5) °C.

The samples are kept in the chamber at a steady temperature of minus (20±5) °C for 4 hours, after which the bags with samples are removed, immersed in a vessel with water at a temperature of 20 °C, and kept for 2 hours.

13.5. Processing the results

Loss of weight of the sample ( P MPZ) as a percentage is calculated using the formula

(28)

Where T - weight of the sample before testing, g;

T 1 - mass of grains sampled on a control sieve with mesh No. 1.25 or 016 after testing, g.

APPLICATION

Information

SCOPE OF TESTING

The name and scope of the tests are indicated in table. 5.

Table 5

	Application area
Test name	Quality control at the manufacturing plant		Geological	Incoming control
	Acceptance	Periodic	Intelligence service	At the consumer enterprise
1. Determination of grain composition and fineness modulus
2. Determination of clay content in lumps
3. Determination of the content of dust and clay particles
4. Determination of the presence of organic impurities
5. Determination of mineralogical and petrographic composition
6. Determination of true density
7. Determination of bulk density and voids
8. Humidity determination
9. Determination of reactivity
10. Determination of the content of sulfate and sulfide compounds
11. Determination of frost resistance of sand from crushing screenings

Note. The “+” sign means that the test is being carried out; sign "– ” - do not carry out.

INFORMATION DATA

1. DEVELOPED AND INTRODUCED by the Ministry of Industry building materials USSR

PERFORMERS

M. L. Nisnevich, Doctor of Engineering. Sciences (topic leader); N. S. Levkova, Ph.D. tech. sciences; E. I. Levina, Ph.D. tech. sciences; G. S. Zarzhitsky, Ph.D. tech. sciences; L. I. Levin; V. N. Tarasova, Ph.D. tech. sciences; A. I. Polyakova; E. A. Antonov; L. V. Bereznitsky, Ph.D. tech. sciences; I. I. Kurbatova Ph.D. tech. sciences; G. P. Abysova; M. F. Semizorov; T. A. Kochneva; A. V. Strelsky; V. I. Novatorov; V. A. Bogoslovsky; T. A. Fironova

2. APPROVED AND ENTERED INTO EFFECT by Resolution of the State Construction Committee of the USSR dated October 5, 1988 No. 203

3. Complies with ST SEV 5446-85, ST SEV 6317-88 (in terms of sampling and determination of grain composition)

4. Instead of GOST 8735-75 and GOST 25589-83

5. REFERENCE REGULATIVE AND TECHNICAL DOCUMENTS

Designation of the referenced technical document	Number of paragraph, subparagraph
GOST 8.326-78	1.10
GOST 83-79	12.2.2.2
GOST 427-75	9.1.2
GOST 450-77	8.1.2; 8.2.2; 12.2.1.2
GOST 1277-75	12.2.1.2
GOST 1770-74
GOST 2184-77	8.1.2; 8.2.2
GOST 2874-82
GOST 3118-77	12.2.1.2; 12.3.2
GOST 3760-79	12.2.1.2
GOST 4108-72	12.2.1.2
GOST 4159-79	12.2.2.2
GOST 4204-77	12.2.2.2
GOST 4220-75	12.2.2.2
GOST 4232-74	12.2.2.2
GOST 4328-77
GOST 4461-77	12.2.1.2
GOST 5072-79	5.1.2, 5.2.2
GOST 6613-86	1.6, 3.2, 4.2, 5.2.2, 7.2, 12.2.1.2, 13.2
GOST 6709-72	8.1.2
GOST 8269-87	2.3, 5.3.1, 5.4.1, 9.1.5, 11, 12.2.1.3
GOST 8736-93	2.11
GOST 9147-80	5.2.2, 8.2.2, 12.2.1.2
GOST 10163-76	12.2.2.2
GOST 22524-77	8.1.2
GOST 23732-79
GOST 23932-90	12.2.1.2
GOST 24104-88	3.2, 4.2, 5.1.2, 5.2.2, 6.2, 7.2, 8.1.2, 8.2.2, 9.1.2, 10.2, 13.2
GOST 25336-82	8.1.2, 8.2.2, 12.2.1.2
GOST 25706-83	4.2, 7.2
GOST 27068-86


Designation	GOST 8735-88
Title in Russian	Sand for construction work. Test methods
Title in English	Sand for construction work. Testing methods
Effective date	01.07.1989
OKS	91.100.15
KGS code	Zh19
OKSTU code	5711
Index of the GRNTI rubricator	670181
Abstract (scope of application)	This standard applies to sand used as a filler for monolithic concrete, prefabricated concrete and reinforced concrete structures, as well as material for corresponding types of construction work, and establishes test methods
Keywords	construction ; filler for monolithic concrete; aggregate for precast concrete structures; filler for reinforced concrete structures; material for relevant types of construction work;
Type of standard	Standards for control methods
Designation of the replacement(s)	GOST 8735-75; GOST 25589-83
Normative references to: GOST	GOST 8.326-89; GOST 83-79; GOST 427-75; GOST 450-77; GOST 1277-75; GOST 1770-74; GOST 2184-77; GOST 2874-82; GOST 3118-77; GOST 3760-79; GOST 4108-72; GOST 4159-79; GOST 4204-77; GOST 4220-75; GOST 4232-74; GOST 4328-77; GOST 4461-77; GOST 6613-86; GOST 6709-72; GOST 8269.0-97; GOST 8736-93; GOST 9147-80; GOST 10163-76; GOST 22524-77; GOST 23732-79; GOST 23932-90; GOST 24104-2001; GOST 25336-82; GOST 25706-83; GOST 27068-86; GOST 29329-92; GOST R 51232-98
Normative references to: Other	TU 6-09-1706-82; TU 6-09-5169-84; PR 50.2.009-94
Document submitted by CIS organization	Ministry of Industry and Construction Materials of the USSR
Rostekhregulirovaniya Department	50 - Ministry of Construction of the Russian Federation
MND developer	Russian Federation
Last edition date	01.11.2006
Change number(s)	reissue with changes 1; 2
Number of pages (original)	26
Organization - Developer	Ministry of Industry and Construction Materials of the USSR
Status	Valid

GOST 873588

(ST SEV 5446 * 85)

ST SEV 6317 * 88