1、Designation: D 1720 03Standard Test Method forDilution Ratio of Active Solvents in Cellulose NitrateSolutions1This standard is issued under the fixed designation D 1720; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of l
2、ast revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1. Scope*1.1 This test method covers the determin
3、ation of the volumeratio of hydrocarbon diluent to active solvent required to causepersistent heterogeneity (precipitation) in a solution of cellu-lose nitrate.1.2 The values stated in SI units are to be regarded as thestandard. The values given in parentheses are for informationonly.1.3 The followi
4、ng applies to all specified limits in thisstandard; for purposes of determining conformance with thisstandard, an observed value or a calculated value shall berounded off “to the nearest unit” in the last right-hand digitused in expressing the specification limit, in accordance withthe rounding-off
5、method of Practice E 29.1.4 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prio
6、r to use. For specific hazardstatements, see Section 6.1.5 For hazard information and guidance, see the suppliersMaterial Safety Data Sheet.2. Referenced Documents2.1 ASTM Standards:2D 301 Test Methods for Soluble Cellulose NitrateD 841 Specification for Nitration Grade TolueneD 4615 Specification f
7、or n-Butyl Acetate (All Grades)E 29 Practice for Using Significant Digits in Test Data toDetermine Conformance with Specifications3. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 dilution ratio, nthe maximum number of unit vol-umes of a diluent that can be added to a unit volum
8、e of solventto cause the first persistent heterogeneity (precipitation) in thesolution at a concentration of 8 g cellulose nitrate per 100 mLof combined solvent plus diluent and at a temperature of 25 63C.NOTE 1The dilution ratio decreases as the cellulose nitrate concen-tration at the end point inc
9、reases. It is, therefore, necessary to set anarbitrary concentration of cellulose nitrate as part of the dilution ratioterm. For this purpose 8.0 g of cellulose nitrate per 100 mL of solvent plusdiluent has been adopted.4. Significance and Use4.1 By use of standard or reference grade materials for a
10、nytwo of the three components, namely, oxygenated solvent,diluent, or cellulose nitrate, the effect of different batches ordifferent types of the third component can be determined.4.2 This test method is applicable for the determination ofthe following:4.2.1 The dilution ratio of toluene as the stan
11、dard diluent toan oxygenated solvent under test, using as the solute standardcellulose nitrate as defined in 5.2.4.2.2 The dilution ratio of a hydrocarbon diluent under testto n-butyl acetate as the standard solvent, using as a solutestandard cellulose nitrate as defined in 5.2.4.2.3 The dilution ra
12、tio of toluene, as the standard diluent, ton-butyl acetate as the standard solvent, using as the solutecellulose nitrate of varying solubility characteristics.4.3 The information developed through this test may beuseful in the formulation of cellulose-based lacquers andadhesives.5. Materials5.1 n-Bu
13、tyl Acetate (90 to 92 %), conforming to Specifi-cation D 4615.NOTE 2This grade of n-butyl acetate contains 8 to 10 % n-butylalcohol.1This test method is under the jurisdiction of ASTM Committee D01 on Paintand Related Coatings, Materials, and Applications and is the direct responsibility ofSubcommit
14、tee D01.35 on Solvents, Plasticizers, and Chemical Intermediates.Current edition approved Dec. 1, 2003. Published December 2003. Originallyapproved in 1960. Last previous edition approved in 1996 as D 1720 96 (2000).2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM
15、 Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshoh
16、ocken, PA 19428-2959, United States.5.2 Cellulose Nitrate, conforming to the Sampling section(Appearance, Ash, and Stability requirements) of Test MethodsD 301 and of such quality that, when used in determining thetoluene dilution ratios of n-butyl acetate and methyl n-propylketone, it will give res
17、ults between the following limits:Toluene Dilution Ration-butyl acetatemethyl n-propyl ketone2.73 to 2.833.80 to 3.905.3 Toluene (Toluol), conforming to Specification D 841.6. Hazards6.1 Soluble cellulose nitrate is a flammable material, thedegree of flammability varying with the extent and nature o
18、fthe wetting medium. Cellulose nitrate is always wet with wateror alcohol in commercial handling, shipping, and storage, inwhich condition it presents no unusual hazard. Dry cellulosenitrate, if ignited by fire, spark, or static electricity, burns veryrapidly. Do not store samples of dry cellulose n
19、itrate at anytime. Dry only that portion required for immediate test. Wear aface shield when the oven is opened after samples have beenheated. Wet excess material and the samples left after testingwith water and dispose of properly.7. Drying Cellulose Nitrate7.1 Dry not more than 20 g of cellulose n
20、itrate at a time byspreading in a thin layer on a tray at room temperature for 12to 16 h, or on top of a 100C oven where the temperature is 35to 40C for about 8 h (Warning, see 6.1). Alternatively, use asteam or hot water-heated oven maintained at 45 to 50C to dryspecimens in about 8 h. For safety r
21、easons, the oven shouldhave the latch removed.7.2 Another simple way to dry small quantities of cellulosenitrate is to use a drier assembled from common laboratoryapparatus. The assembled drier is shown in Fig. 1. Hot air froma laboratory electric oven is drawn through wet cellulosenitrate contained
22、 in a brass tube hooked up through a thistletube, or small funnel, and suction flask to a water aspirator orother vacuum source. The brass pipe should be about 40 mm indiameter and 200 mm long, these relative dimensions havingbeen found to give efficient results. Such a tube will hold about25 g, dry
23、 weight, of wet cellulose nitrate. The pipe is insulatedto conserve heat. The suction flask end of the brass tube is fittedwith a thistle tube, or a small funnel, over the mouth of whichis tied a silk cloth screen. An indentation made in the funneledge allows insertion of the thermometer. The funnel
24、 andthermometer are held in place by means of a rubber stopper.When using an oven temperature of 85C and vacuum suppliedby a water aspirator or other vacuum source, the alcohol-wetcellulose nitrate will be dried in about 4 h.7.3 If larger quantities of cellulose nitrate are required, thedrying equip
25、ment described in the Procedure section of DryingSamples of Test Methods D 301 may be used.8. Preparation of Solution8.1 When testing either a solvent or diluent, first estimatethe probable dilution ratio for the unknown component inrelation to the other to determine the amount of solventrequired to
26、 dissolve the cellulose nitrate (Table 1). This volumeof solvent should be such that there will be approximately 10 gof cellulose nitrate present per 100 mL of solvent plus diluentat the end point.NOTE 3Reference to published data on similar types of solvents ordiluents will provide a good approxima
27、tion of the amount of solventrequired. If data are not available, several solutions with varying amountsof solvents may be required to arrive at a suitable volume to use.8.2 On an analytical balance, weigh 5 6 0.01 g of thecellulose nitrate into a 125-mL cork-stoppered, preweighedErlenmeyer flask, o
28、r other suitable container. From a buret addthe volume of solvent indicated in Table 1. Swirl the flask untilthe cellulose nitrate is completely dissolved. When a highconcentration of cellulose nitrate in solvent is required, disper-sion may be more quickly accomplished by adding a measuredportion o
29、f the diluent to the flask. This reduces the solidsconcentration and thus lowers the viscosity of the solution,making it easier to dissolve the cellulose nitrate.9. Procedure9.1 Add the diluent, maintained at 25 6 3.0C, to the flaskfrom a buret in small additions. Five-millilitre increments maybe ad
30、ded at first, but these shall be decreased to about 0.5 mLas the end point is approached. After each addition, stopper theflask and swirl vigorously to disperse any gel or precipitatethrown down by local overconcentration of diluent (Note 4).When precipitation persists after at least 2 min of vigoro
31、usswirling, the initial end point has been reached, as indicated bythe presence of gel particles in the solution or on the sides ofthe flask (Note 5). Determine the total volume of diluent addedto the flask at this point.NOTE 4Take care to prevent loss of volatile components by evapo-ration. Avoid c
32、ontact of the solution with the stopper.NOTE 5Presence of a uniform fine haze that is usually formed whenaliphatic hydrocarbons are used as diluents must not be confused with thegel end point.FIG. 1 Assembled DrierD17200329.2 Determine a second end point using the same solution.This requires additio
33、n of solvent to redissolve the cellulosenitrate. The amount of solvent to add depends upon the amountof diluent used in the initial titration. The volume of solvent tobe added is obtained directly from Fig. 2 and the volume ofdiluent used to reach the initial end point.9.3 After addition of the requ
34、ired volume of solvent, swirlthe flask to redisperse the cellulose nitrate. Then, continue thetitration with diluent to the second end point, at which pointthere should be approximately 8 g of cellulose nitrate presentper 100 mL of solvent plus diluent.10. Calculation10.1 Calculate the dilution rati
35、o and cellulose nitrate con-centration at both the initial and the second end points asfollows:Dilution ratio 5 A/B (1)Cellulose nitrate concentration per 100 mL of volatile matter 5C/A 1 B!where:A = diluent for the titration, mL,B = solvent used, mL, andC = cellulose nitrate used, g.10.2 Construct
36、a graph for dilution ratio versus cellulosenitrate concentration. Plot as two points on the graph (Fig. 3)the two sets of values calculated as described in 10.1. One ofthe points will be very close to 8 g/100 mL of volatile matter.The correct value at exactly 8 g/100 mL of volatile matter maybe inte
37、rpolated by drawing a straight line connecting the twoexperimentally determined points. While the curve showingthe relationship between the dilution ratio and cellulose nitrateconcentration is not necessarily a straight line, the error madeby interpolating or extrapolating from the straight line con
38、nect-ing the two points is negligible in the proximity of 8 6 1 g/100mL of volatile matter.NOTE 6Example: Assuming a probable dilution ratio of approxi-mately 3, the following results are obtained:SolventInitial Added SecondEnd (from EndPoint Fig. 2) PointCellulose nitrate, g 5.00 . 5.00Solvent, mL
39、12.5 3 15.5Diluent, mL 35.0 . 49.6Solvent plus diluent, mL 47.5 . 65.1Dilution ratio 35/12.5 = 2.8 . 49.6/15.5= 3.2Cellulose nitrate per 100 mL ofvolatile matter, g10.5 . 7.7From Fig. 3 the dilution ratio at 8.0 g of cellulose nitrate = 3.1611. Report11.1 When testing solvents, report the ratio of t
40、he volume oftoluene to the volume of solvent at 8 g of cellulose nitrate per100 mL of volatile matter.11.2 When testing diluents, report the ratio of the volume ofdiluent to the volume of n-butyl acetate at 8 g of cellulosenitrate per 100 mL of volatile matter.11.3 When testing cellulose nitrate, re
41、port the ratio of thevolume of toluene to the volume of n-butyl acetate at 8 g ofcellulose nitrate per 100 mL of volatile matter.12. Precision and Bias12.1 PrecisionThe following criteria should be used forjudging the acceptability of results at the 95 % confidencelevel.12.1.1 RepeatabilityTwo resul
42、ts obtained by the sameoperator should be considered suspect if they differ by morethan 0.1.12.1.2 ReproducibilityTwo results obtained by operatorsin different laboratories should be considered suspect if theydiffer by more than 0.2.12.2 BiasThis test method has no bias because the valueof the test
43、result is defined only in terms of the test method.13. Keywords13.1 active solvents; cellulose nitrate solutions; dilutionratio; hydrocarbon diluentTABLE 1 Volume of Solvent Required to Dissolve CelluloseNitrateProbable Dilution Ratio, volume ofdiluent:volume of solventmL of Solvent per5gofCellulose
44、Nitrate at 25C1 25.02 16.73 12.54 10.05 8.3FIG. 2 Volume of Solvent to Be Added to Complete Titrationversus Volume of Diluent Used to Reach Initial End PointFIG. 3 Grams of Cellulose Nitrate per 100 mL of Volatile Matterversus Dilution RatioD1720033SUMMARY OF CHANGESCommittee D01.35 has identified t
45、he location of selected changes to this standard since the last issue(D 1720 96 (2000) that may impact the use of this standard.(1) Added reference to Practice E 29 in 1.3 of the Scopesection.(2) Added Practice E 29 to the list of Referenced Documents.(3) Added statement to Significance and Use sect
46、ion to showapplicability to lacquers and adhesives.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent righ
47、ts, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for
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49、you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).D1720034
