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IS 13030: Method of test for laboratory determination of water content, porosity, density and related properties of rock material PDF

13 Pages·1991·1.5 MB·English
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Preview IS 13030: Method of test for laboratory determination of water content, porosity, density and related properties of rock material

इंटरनेट मानक Disclosure to Promote the Right To Information Whereas the Parliament of India has set out to provide a practical regime of right to information for citizens to secure access to information under the control of public authorities, in order to promote transparency and accountability in the working of every public authority, and whereas the attached publication of the Bureau of Indian Standards is of particular interest to the public, particularly disadvantaged communities and those engaged in the pursuit of education and knowledge, the attached public safety standard is made available to promote the timely dissemination of this information in an accurate manner to the public. “जान1 का अ+धकार, जी1 का अ+धकार” “प0रा1 को छोड न’ 5 तरफ” Mazdoor Kisan Shakti Sangathan Jawaharlal Nehru “The Right to Information, The Right to Live” “Step Out From the Old to the New” IS 13030 (1991): Method of test for laboratory determination of water content, porosity, density and related properties of rock material [CED 48: Rock Mechanics] “!ान $ एक न’ भारत का +नम-ण” Satyanarayan Gangaram Pitroda ““IInnvveenntt aa NNeeww IInnddiiaa UUssiinngg KKnnoowwlleeddggee”” “!ान एक ऐसा खजाना > जो कभी च0राया नहB जा सकता हहहहै””ै” Bhartṛhari—Nītiśatakam “Knowledge is such a treasure which cannot be stolen” IS 13030 : 1991 ‘ye2 qSfq” WTef Jv=m “RE~AFFIRMED 19%” Indian Standard’ METHODOFTESTFOR LABORATORYDETERMINATIONOF WATERCONTENT,POROSITY,DENSlTYAND RELATED PROPERTIESOFROCK MATERIAL UDC 624.121~43 ” m BIS 1991 BUREAU OF INDIAN STANDARDS MANAK BHAVAN, 9 BAHADUR SHAH ZAFAR MARG NEW DELHI 110002 Muy 1991 Price Group 3 Rock Mechanics Sectional Committee, CED 48 . FOREWORD This Indian Standard was adopted by the Bureau of Indian Standards, after the draft finalized by the Rock Mechanics Sectional Committee had been approved by the Civil Engineering Division Council. The presence of pores in fabric of a rock material decreases its strength and increases its deformability. A small volume fraction of pores can produce an appreciable mechanical effect. Information on the porous nature of rock materials is frequently omitted from petrological descriptions but is required if these descriptions are to be used as a guide to mechanical performance. Sand stones and carbonate rocks in particular occur with a wide range of porosities and hence of mechanical character; igneous rocks that have been weakened by weathering processes also have typically high porosities. Most rocks have similar grain densities and therefore have porosity and dry density values that are highly correlated. A low density rock is usually highly porous. It is often sufficient, therefore, to quote values for porosity alone but a complete description requires .values for both porosity and density. Different methods of determination of density and porobity described in the standard are suitable for different types of rocks and sample, While method using saturation and caliper technique and using satu- ration and buoyancy technique are suitable for regular and irregular shape of sample respectively of those rocks which do not appreciably swell or disintegrate when immersed in water, the method using mercury displacement and grain specific gravity technique is suitable for irregular shape of such rock which are liable to swell or disintegrate when immersed in water. These methods are based on the suggested method of International Society of Rock Mechanics. In reporting the results of a test or analysis made in accordance with this standard, if the final value, observed or calculated, is to be rounded off, it shall be done in accordance with IS 2 : 1960 ‘Rules for rounding off numerical values ( rsvised )‘- IS 18030: 1991 I&& Stan&-& .~’ . ~. METHODOFTESTFOR LABORATORYDETERMINATIONOF WATERCONTENT,POROSITY,DENSITYAND RELATED PROPERTIESOFROCKMATERIAL 1 SCOPE 2.2.6 Porosity n = -> x 100 ( percent ) This standard gives the procedure for the test to evaluate water content, porosity, density and 2.2.7 Void Ratio e = + related properties of rock material. The following 8 test methods have been covered: 2.2.8 Density or Bulk Density or Mass Density a) Determination of the water content of rock (p)LLL”qMw sample; kg/m3 b) Determination of porosity and density using saturation and caliper technique; 2.2.9 Relative Density c) Determination of porosity and density using saturation and buoyancy; and ( mass specific gravity ) G, e c d) Determination of porosity and density using mercury displacement and grain specific 2.2.10 Dry density pa= z;- kg/m3 gravity technique. 2 DEFXNITIONS AND SYMBOLS 2.2.11 Dry Relative Density 2.1 Symbols ( dry specific gravity ) Ge = 2 For the purpose of this standard unless otherwise defined in the text, the following symbols shall 2.2.12 Saturated Density apply: MS + : wP‘ kg/m3 tssp = SM - Mass of grain ( the solid component of the sample ) - 8-v = Volume of grain 2.2.13 Saturated Relative Density Psat M, = Mass of pore water ( saturated specific gravity ) G,, = ~ Pw p, = Volume of pore water 2.2.14 Solid Density or Density P, = Density of water MS V, = Volume of pore air of Rock Material ps = -v- kg/ms 8 2.2 Definitions 2.2.15 Solid Relative density For the purpose of this standard, physical proper- ties pertinent to the methods of test shall be ( solid specific grgvity ) Gs = -$ described as follows. 2.2.1 Bulk Sample Mass M = MS + M, 2.2.16 Unit Weight y = P x g N/m3 2.2.2 Bulk Sample Volume V = Vi + Vv 3. TEST SAMPLE 2.2.3 Pore ( Voids ) Volume V, = VW + V, A representative sample for testing should 2.2.4 Water Content, w generally comprise several rock lumps, each in MW order of magnitude larger than the largest grain = - X 100 (percent ) or pore size. Microfissures of similar size to that MS of a rock will cause erratic results, their presence 2.2.5 Degree of Saturation, Sr should be noted and if possible the lump size increased or reduced to specifically include or = + x 100 ( percent ) P exclude the influence of such fissures. 4 DETERMINATION OF THE WATER 4.4.2 The water content should be reported to the CONTENT OF A ROCK SAMPLE nearest O-1 percent stating whether this corres- ponds to in situ water content, in which case 4.1 Object precautions taken to retain water during sampling This method of test covers the procedure of deter- and storage should be specified. mining the mass of water contained in a rock 5 POROSITY AND DENSITY sample as a percentage of the oven dry sample DETERMINATION USING SATURATION mass. AND CALIPER TECHNIQUES 4.2 Apparatus 5.1 Object 4 An oven capable of maintaining a tempera- 5.1.1 This method of test covers the procedure for ture of 105 f 3°C for a period of at least determining the porosity and dry density of rock 24 h. samples in the form of specimen of regular geome- b) A sample container non-corrodible material try. including an airtight lid. 5.1.2 The method is applicable only to nonfriable lC A desiccator to hold sample container coherent rocks that can be machined and do not during cooling. appreciably swell or disintegrate when they are 4 oven dried or are immersed in water. The method A balance of adequate capacity, capable of is suitable when regularly shaped specimens are weighing to an accuracy of 0.01 percent of required for other test purposes. the sample mass. 5.2 Apparatus 4.3 Procedure 4 An oven capable of maintaining a tempera- 4.3.1 The container with its lid is cleaned and ture of 105 & 3°C for a period of at least dried, and its mass m, is determined. 24 h. b) A desiccator to hold specimen during 4.3.2 A representative sample comprised at least cooling. 10 lumps each having either a mass of at least 50 g or a minimum dimensions of ten times the maxi- C> A measuring instrument such as vernier or mum grain size, whichever is greater, is selected. micrometer caliper, capable of reading For in situ water content determination sampling, specimen dimensions to an accuracy of storage and handling precautions should be such 0.1 mm. that water content remains within 1 percent of 4 Vacuum saturation equipment such that the in situ value. the specimen can be immersed in water under a vacuum of less than 0.8 kPa for a 4.3.3 The sample is placed in the container, the period of‘ at least one hour. lid replaced and the mass ma of the sample plus e) container determined. A sample container of non-corrodible mate- rial, including an airtight lid. 4.3.4 The lid is removed and the sample dried to f 1 A balance of adequate capacity for deter- constant mass at a temperature of 105 f 3°C. mining the mass of a specimen to an 4.3.5 The lid is replaced and the sample allowed accuracy of 0.01 percent of the specimen to cool in the desiccator for 30 minutes. The mass mass. m3 of sample plus container is determined. 5.3 Procedure 4.4 Calculation and Reporting of Results 5.3.1 Select at least three specimens from a representative sample of material. Machine each 4.4.1 The water content shall be calculated from specimen to conform closely to the geometry of a the following formula: right cylinder or prism. The minjmum size of each specimen should either be such that its mass Water content, w is at least 50 g ( for an average density rock a cube with sides of 27 mm will have sufficient Pore water mass AI, = x 100 ( percent ) mass ) or such that its minimum dimension is at Grain mass Ma least ten times the maximum grain size, whichever m3 - m3 is the greater. = -- X 100 ( percent ) ms - ml 5.3.2 Repeat the following procedure for each of the specimen in the sample: m, = Mass in g of the container with its lid at room temperature i) Determine the external dimension and then bulk volume voof each specimen with the m2 = Mass in g of the container with its lid vernier or calipers. Measurement should and the sample at room temperature be accurate to 0.1 mm. An average of three m3 - Mass in g of the container with its lid separate measurement should be obtained and the sample after drying for each dimension. 2 IS il3030: 1991 b! ii) Place the specimen in an oven and dry at Report that the bulk volume was obtained 105 f 3°C. For this test method specimens by measurement of dimension by caliper or should be of sufficient coherence not to vernier and the pore volume was obtained require containers, but these should be by water saturation. used if the rock is at all friable or fissible. cl Record any change in the shape and size of The specimen is deemed to be dry when the rock specimen during wetting or the difference between successive deter- drying. minations of mass of the cooled specimen 4 Record the following general information: at intervals of 4 hours does not exceed 0.1 percent of the original mass of the speci- i) Project title. men. ii) Sampling technique and sample identi- iii) Remove the specimen from the oven and fications number. place in a desiccator to cool. iii) Dates of sampling and of testing. iv) Determine the dry mass, &I~, of the speci- iv) Lithological description of the rock men. samples. v) Immerse the specimen in a container of water and place the container with the 6 POROSITY AND DENSITY specimen in a vacuum of less than O-8 kPa DETERMINATION USING SATURATION for a period of one hour with periodic AND BUOYANCY TECHNIQUES agitation to remove trapped air. 6.1 Object vi) Determine the water temperature, t, to the nearest degree centigrade. This method of test covers the procedure for determining the porosity and the dry density of a vii) Remove the specimen from the container rock sample in the form of lumps or aggregate of and surface dry it using a moist cloth. irregular shape-geometry. It may also be applied Care should be taken to remove only surface to a sample in the form of specimens of irregular water and to ensure that no fragments geometry. are lost. viii) Determine the saturation mass, Msat, of the 6.1.1 The method should only be used for rocks specimen. that do not appreciably swell or disintegrate when oven-dried and immersed in water. -5.4 Calculations 6.2 Apparatus a) For each specimen calculate the pore volume, VV, by the following formula: 4 An oven capable of maintaining a tempera- ture of 105 f 3% for a period of at least VV = M”“t-, Ma 24 h. A sample container of non-corrodible where pw = density of water at tempera- material, including an air-tight lid. ture, t. b) A desiccator to hold sample container For each specimen calculate the bulk during cooling. volume, V, from the external dimensions. A vacuum vessel such that the sample can c) For each specimen calculate the dry density, be immersed in water under a vacuum of Fd, by the following formula: less than 0.8 kPa for a period of at least 1 h. Fd = + ( kg/m3 ) e) A balance of adequate capacity, capable of 4 For each specimen calculate the porosity, n, weighing to an accuracy of 0.01 percent of by the following formula: the sample weight. Vv f 1 An immersion bath and a wire basket or n=--- v x 100 ( percent ) perforated container, such that the sample )e Calculate average values of porosity and immersed in water can be freely suspended from the stirrup of the balance to deter- dry density for the sample. mine the saturated-submerged weight. The 5.5 Reporting of Results basket should be suspended from the balance by a fine wire so that only the wire a) Report the individual dry density and intersects the water surface in the immer- porosity values for each specimen in the sion bath. sample, together with the average values of dry density and porosity for the sample. 6.3 Procedure Density values should be given to the nearest 10 kg/m3 and porosity values to a) A representative sample comprising at least the nearest 0.1 percent. 10 lumps of regular or irregular geometry, 3 c IS 13030 i 1991 each having either a mass of at least 50 g Determination .A%. .(I) (2) (3) or a minimum dimension of at least 10 times the maximum grain size, whichever 4) Saturated surface dry is the greater, is selected. The sample is mass of the sample washed in water to remove dust. plus container, Mq b) The sample is saturated by water immer- in kg sion in a vacuum of less than 0,s kPa for a 5) Dried mass of the period of at least 1 h, with periodic container with sam- agitation to remove trapped air. c> ple, Mb in kg Determine the temperature, t, of the water 6.5 Calculations in the immersion bath to the nearest degree centigrade. a) Calculate the saturated-submerged mass, 4 Determine the mass, MI, of the basket sub- Msub, of the sample merged in the immersion bath. e> M sub = MB - Ml ( kg ) Transfer the sample under water to the b) Calculate the saturated-surface-dry mass, basket in the immersion bath. Determine Msat, of the sample the saturated-submerged mass, M,, of the basket plus sample to an accuracy of 0.01 &at = M4 - ~43 ( kg > percent of the sample mass. lC Calculate the dry mass ( Grain Weight ) f 1 Determine the mass, Ma, of a clean, dry MS, of the sample d Rsaemmpovlee ctohnet ainsearm plaen d frloidm. the immersion 4 CalculaMtes = thMe b b- ulkM-Sv olu( mkeg , 1 V, of the bath and surface dry the sample with a sample by the following formula: moist cloth, care being taken to remove only surface water and to ensure that no v tasM - busM >( m3 1 C rock fragment are lost. Transfer the sample PW to the sample container and replace the Pw = density of water at temperature t lid. Determine the mass, M1, of the satura- 4 ted surface dry sample plus container. Calculate the pore volume, V, of the sample h) Remove the lid and place the container by following formula: with contents and lid in the oven and dry ta& - SM V =v ( ms 1 at 105 & 3°C. The sample is deemed to > PW be dry when the difference between succes- f > Calculate porosity, n, of the rock sample sive determination of mass of the cooled by the following formula : sample at interval of 4 hours does not exceed 0.1 percent of the original mass of n = ( V,/V) x 100 (percent) the sample. or = ta&l - MS x 100 ( percent ) )i. Replace the lid, remove th e container from Meat - Msub > the oven and place the whole in the desic- g) Calculate the dry density, Pa, of the rock cator to cool for 30 minutes. sample by the following formula: k) Determine the dried mass, MS, of the con- ( kg/m3 1 tainer with the oven dry sample. Pd = + 6.4 Observations 6.6 Reporting of Result 4 Sample No. Date Report the porosity and dry density values or the sample to the nearest O-1 percent Temperature of water, t, in Centigrade and 10 kg/m5 respectively. b) Report that the bulk volume was obtained Determination .No. (1) (2) (3) by a buoyancy technique and that the pore 1) volume was obtained by water saturation. Saturated-submerged c j mass of basket alone, Report the following general information: MI in kg i) Project title 2) Saturated-submerged ii) Sampling technique and sample identi- mass of basket + fication numbers specimen, Ma in kg iii) Date of sampling and testing 3) Mass of container and iv) Lithological description of the rock lid, MS in kg samples. 4 IS 13030 : 1991 7 POROSITY AND DENSITY b) Repeat the following procedure for each of DETERMINATION USING MERCURY the specimens in the sampie: DISPLACEMENT AND GRAIN SPECIFIC 9 Brush each specimen to remove loose GRAVITY TECHNIQUES material and measure its volume, V, by mercury displacement. 7.1 Object . ii) Carefully remove mercury adhering to 4 the sample, ensuring that no rock frag- This method of test covers the procedure ment are lost. for determining the porosity and the density of a rock sample in the form of lumps or iii) Determine the mass, MI, of a suitable aggregate of irregular geometry. clean, dry, container and its lid. b) This is particularly suitable if the rock iv) Place the specimen in the container, material is liable to swell or disintegrate if replace the lid and determine the mass, immersed in water. The test is also appli- M,, of the container plus specimen at cable to regularly shaped rock specimens or imtral water content. to coherent rock materials but other tech- IV Remove the lid and the specimen is niques are usually found more convenient oven dried to constant mass at a tem- in these cases. perature of 105 f 3°C allowed to cool tbr 30 minutes in a desiccator, The mass, 7.2 Apparatus MS, of container plus oven dry specimen a) An oven capable of maintaining a tempera- is determined. lc ture of 105 & 3°C for a period of at least Crush all the rock specimens and grind to 24 h. It should have forced ventilation a grain size not exceeding 150 mm. A exhausting to outside atmosphere. number of representative sub-samples of b) Specimen containers of non-corrodible about 15 g of the pulverized material are selected and oven-dried. material, including airtight lids. c> 4 Determine the mass, M,, of a clean, dry A desiccator to hold specimen containers volumetric flask plus stopper to an accuracy during cooling. of 0.001 g. d) A balance of adequate capacity, capable of e> Fill the flask with a liquid such as kerosene mass determination to 0.01 percent of that is non-reactive with the rock. sample mass. e) A mercury-displacement volume measuring f) Bring the flask to equilibrium temperature in the constant temperature bath and apparatus capable of measuring specimen adjust the liquid level accurately to the volume to 0.5 percent. f 1 Grinding equipment to reduce the sample 50 ems graduation. Remove the flask from the constant temperature bath, insert the to a pulverized powder less than 150 mm in stopper and clean and dry the outside of grain size. the flask. d A calibrated volumetric flask and stopper Determine the mass, ME, of the flask and ( conveniently 50 ems ). iiquld to an accuracy of 0.01 percent of the 4 A constant temperature water bath. total mass. )j A vacuum apparatus capable of maintain- h) Empty and dry the flask and add the ing a vacuum with a pressure of less than representative 15 g sub-sample of dry pul- 0.8 kPa. verized rock with the aid of a funnel. k) A soft brush of camel hair or of similar >j Determine the mass, MB, of flask, sample softness. and stopper to an accuracy of O*OOl g. 7.3 Procedure k) The flask and sub+ample are evacuated for about 20 minutes and sufficient fluid added 4 A representative sample is selected compris- to thoroughly wet the sample. Further ing at least ten rock lumps, the shape and fluid is then added and the flask IS carefully size of lumps suiting the capabilities of the evacuated to remove air. The flask is volume measuring apparatus. The minimum replaced in the constant temperature water size of each lump should preferably be bath and the liquid level adjusted accura- either such that its mass exceeds 50 g or tely to the 50 ems graduation. such that its minimum dimension is at least 4 The stoppered flask with its contents is 10 times the maximum grain size, which- allowed to cool and its mass, G, is deter- ever is the greater. Specimen and swelling mined to 0.01 percent of the total mass. or fissible rock should be sampled and stoned to retain water content to within 1 percent 4 Steps (e) to (m) are repeated for each sub- of its in situ value prior to testing. sample of pulverized material. 5

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