1、Designation: C614 10Standard Test Method forAlkali Resistance of Porcelain Enamels1This standard is issued under the fixed designation C614; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in par
2、entheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.INTRODUCTIONAlthough all porcelain enamels are highly resistant to atttack by cold alkaline solutions, somecompositions are affected by hot solutions of the typ
3、e encountered in automatic laundry anddishwashing equipment. Tests to eliminate porcelain enamels of poor resistance have been developedand used by various laboratories. In general, these tests consist of subjecting specimens to a boilingsolution of either sodium pyrophosphate or sodium hydroxide fo
4、r a period of two or more hours. Thespecimens are weighed before and after exposure to the test treatment and the loss-in-weight is takenas a measure of alkali attack. In some tests representing milder exposure conditions, the 45 degreespecular gloss is measured before and after exposure and the per
5、centage of initial gloss retained is usedas an indicator of alkali resistance. While such tests have served a useful purpose in developing moreresistant porcelain enamel compositions and in manufacturing control operations, agreement betweenlaboratories has left something to be desired. The present
6、test was designed to provide thereproducibility between laboratories that is so essential to any standard test procedure.1. Scope1.1 This test method2covers the measurement of the resis-tance of a porcelain enamel to a hot solution of tetrasodiumpyrophosphate. Although the specific alkali mentioned
7、hereinis tetrasodium pyrophosphate the equipment and techniques areequally applicable to other alkali solutions.1.2 The values stated in inch-pound units are to be regardedas standard. The values given in parentheses are mathematicalconversions to SI units that are provided for information onlyand a
8、re not considered standard.1.3 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 p
9、rior to use.2. Significance and Use2.1 This test method is intended specifically for testing theresistance to alkaline attack of porcelain enamels to be used asa final finish on washing machines, dishwashers, combinationwasher-dryers, and similar appliances where the surface isnormally exposed to an
10、 alkaline environment at elevatedtemperatures.3. Apparatus3.1 Test Chamber, of a type illustrated in Fig. 1, Fig. 3, andFig. 6. This part of the equipment consists of a stainless steelbeaker fitted with an O-ring sealed cover which supports animmersion heater, a stirring device, thermometer and ther
11、-mistor wells; three specimen holders; a reflux condenser; aflow channeling shield to slide over and be supported by theimmersion heater; and a stirring motor.3The beaker, heatersheath, stirring device, thermometer and thermistor wells,specimen holders, and the flow channeling shield shall be madefr
12、om stainless steel alloys from the AISI 300 Series.3.2 Temperature Controller, thermistor-actuated, capable ofmaintaining the temperature of the alkali solution in the beakerat 96.00 6 0.20C.3.3 Thermometer, calibrated, approximately 15 in. (380mm) long and932 in. (7.1 mm) in diameter, with 0.1 divi
13、sions.3.4 Drying Oven, electrically heated.3.5 Balance, having a sensitivity of 0.1 mg and a capacity ofnot less than 200 g.3.6 Desiccator.3.7 Hot Plate, or burner suitable for heating the test solu-tion.1This test method is under the jurisdiction ofASTM Committee B08 on Metallicand Inorganic Coatin
14、gs and is the direct responsibility of Subcommittee B08.12 onMaterials for Porcelain Enamel and Ceramic-Metal Systems.Current edition approved Nov. 1, 2010. Published November 2010. Originallyapproved in 1968. Last previous edition approved in 2005 as C614 74 (2005).DOI: 10.1520/C0614-10.2This test
15、was developed at the National Bureau of Standards under thesponsorship of The Porcelain Enamel Institute, Inc., and published as P. E. I.Bulletin T-25.3See the appendix for drawings of the equipment. This equipment may bepurchased from the Hoover Instrument Service, Inc., 401 N. Home Rd.,Mansfield,O
16、H 44906.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.3.8 Sponge, soft, cellulose.3.9 Aluminum Alloy Sheets, approximately 312 by 312 by18in. (89 by 89 by 3.1 mm).4. Reagents and Materials4.1 Tetrasodium Pyrophosphate, hydrated (Na
17、4P2O710H2O), recrystallized, reagent grade.4.2 Trisodium Phosphate (Na3PO412H2O).5. Test Specimens5.1 Preparation of Specimens The test specimens shallbe 312 in. (89 mm) square and may be prepared by enamelingmetal blanks of that size or by cutting from a larger piece.Hanging holes, if necessary for
18、 firing or weighing or both, maybe placed at the corners. The specimens shall be sufficiently flatto permit sealing in the holders. The edges of cut specimensshall be stoned or filed to remove any sharp or loosely adheringfragments of metal or porcelain enamel. It is recommended thatthe specimens be
19、 permanently marked on the back side foridentification.5.2 Number of SpecimensSix specimens shall be testedsimultaneously.5.3 Cleaning of Specimens Before Alkali ExposureThespecimens shall be rinsed with running tap water and washedwith a soft cellulose sponge dampened with a 1 % solution oftrisodiu
20、m phosphate. A light pressure and a back-and-forthmotion in two directions, 90 apart, shall be used in thewashing.After washing, the specimens shall be rinsed first withrunning tap water, next with distilled water and then allowed todrain in a near vertical position prior to oven-drying at 110Cfor 1
21、5 min. The specimens shall be cooled in a desiccator for30 min prior to weighing.5.4 Weighing of Test SpecimensThe specimens shall beweighed immediately upon removal from the desiccator.Weights shall be recorded to 0.0001 g. The weighed specimensshall be stored in a desiccator until tested.6. Proced
22、ure6.1 Preparation of Test SolutionPrepare the test solutionby adding 260 g of tetrasodium pyrophosphate to 4.940 litresof distilled water. Pour the entire amount of prepared solutioninto the beaker and cover the rectangular slots with lids. Use afreshly prepared solution for each set of six specime
23、ns.6.2 Preheating Test SolutionPlace the temperature con-troller and stirrer in operation and preheat the solution to 96C.Heating may be expedited by placing the beaker on a hot plateor over a gas burner. When a temperature near 96C has beenreached, remove the beaker from the hot plate and place on
24、aninsulated surface. Allow an equilibration period of 15 min forall parts of the equipment to achieve a stable temperature, andadjustment of the control point to yield the desired tempera-ture.6.3 Preparation for Alkali Exposure Place two clean,weighed specimens in each specimen-holder box. Shims ma
25、ybe useful in the bottom of the specimen boxes to center thespecimens vertically about the exposure openings. Back-upeach specimen with a stress distributing aluminum alloybacking sheet and insert the clamping device between the twosheets. Tighten the clamping device only enough to give aleakproof s
26、eal. Test the seal by filling the specimen box withwater to confirm the absence of leaks. Next, remove the waterand preheat the specimen holder assembly in an oven at 110Cfor about 15 min.NOTE 1Test solution is in stainless steel beaker.FIG. 1 Alkali Equipment in OperationC614 1026.4 Exposure of Spe
27、cimensWhen the test solution hasreached 96C and is under control, remove the lids and insertpreheated specimen holder assemblies in the proper openings.Expose six specimens for6hat966 0.20C. The exposuretime shall start upon insertion of the specimen holders and shallend with their withdrawal. After
28、 removal from the holdersclean, dry and weigh the specimens as specified in 5.3 and 5.4.6.5 Measurement of Exposed AreaCalculate the area ofthe etched portion of the specimen using the average of twodiameters, approximately 90 apart, which have been measuredto the nearest 0.01 in. (0.25 mm).7. Calcu
29、lation7.1 Calculate the weight loss for each specimen as follows:L, mg/in.25 B C! 3 103/D (1)orL, mg/cm25 B C! 3 103/E (2)where:L = weight loss,B = original weight of specimen, g,C = final weight of specimen, g,D = area of etched attack, in.2(0.155 3 cm2), andE = area of etched attack, cm2(6.45 3 in
30、.2).8. Treatment of Data8.1 Single DeterminationSix specimens shall constitute asample. The average of six values of weight loss (L), shall betermed the mean weight loss, L, for the sample. The statisticalerror of the determination shall be computed by the use of theequation:Dimension in. mmA 9 229B
31、14 6.4CThermistor well1132 8.7 OD818 206 lengthDThermometer well38 9.2 OD818 206 lengthE12 12.7F112 38.0GHeater chuck58 15.9H114 32.0I11732 39.0J158 41.5K78 22.2L378 98M11532 37.5N218 54FIG. 2 Cover for Alkali EquipmentC614 103e 5 1.15 s (3)where:e = the statistical error of the mean value for the s
32、ample,at the 95 % confidence level, ands = the standard deviation of the six individual weightlosses from the average of all six weights.NOTE 1The factor 1.15 is applied only when the number of specimensis six, and the confidence level is 95 %.8.1.1 This standard deviation shall be computed from the
33、generalized equation:s5=(X2/n! X2(4)or if the number of specimens, n, is six, from:s5=(X2/6! X2(5)where:(X2= sum of the squares of the weight loss values of thesix individual specimens, andX2= the square of the mean weight loss of the sixspecimens.8.1.2 Illustrative calculations are given below. The
34、 recom-mended number of decimal places is given in each case:Specimen No. L, mg/in.2L21 7.7 59.292 7.5 56.253 6.9 47.614 8.0 64.005 7.7 59.296 7.9 62.41Sum 45.7 348.85Mean 7.6167 58.1417from Eq 3:s5=58.1417 2 7.6167!25 =0.1276 5 0.357 (6)from Eq 1:e 5 1.15 3 0.357 5 0.411 (7)The weight loss Lis repo
35、rted as 7.66 0.4 mg/in28.2 Difference Between Two DeterminationsThe signifi-cance of a difference between two mean values shall be testedthrough the use of the ratio d:e8A Empty specimen holder in position.B Immersion heater.C Thermometer well.D Thermistor well.E Stirrer.F Circular shield (lowered f
36、or clarity).FIG. 3 Cover AssemblyC614 104where:d = the difference in means, ande8 = the statistical error in the determination of d.8.2.1 The statistical error, e8, of the difference, d, betweentwo means shall be determined from the following equation:e8 5 =e1!21 e2!2(8)where:e8 = the error of the d
37、ifference in means,e1= the error of one mean value, ande2= the error of the other mean value.8.2.2 An example to illustrate the use of Eq 4 is givenbelow:Dimension in. mmA3116 78B 1 25.4C178 47.5D716 11.1E316 4.75F116 1.59G712 190H512 140I612 165J 9 229K 9.8 249L316 4.75M1014 260N12 12.7O516 7.9P12
38、12.7Q34 19.0R2 51FIG. 4 Alkali Test EquipmentC614 105Dimension in. mmA414 108B334 95C1764 6.7D11132 34.0E178 47.5F 0.079 2.01G14 6.4H 6 152I 8 203J332 2.40K18 3.18L212 64M234 70N3 76P 0.060 1.52NOTE 1Box welded from 14-gage (0.079 in.) stainless steel.FIG. 5 Detail Specimen HolderAShowing a specimen
39、.BThe back-up plate.CO-ring interior.DClamping plate (partly withdrawn).FIG. 6 Specimen Holder AssemblyC614 106Assume:L1= 7.66 0.5,L2= 8.26 0.3, andd = 0.6.Then:e8 5 =0.5!21 0.3!25 =0.34 5 0.58 (9)d/e8 5 0.6/0.58 5 1.03When d:e8 is equal to or greater than 1.00, the difference issignificant at the 9
40、5 % confidence level.8.2.3 The following table shows the relation between valuesof d:e8 and the confidence level, for samples of six specimens.d:e8ConfidenceLevel, % InterpretationOver 1.50 99 or higher highly significantOver 1.00 but less 95 to 99 significantthan 1.50 90 to 95 indicativeOver 0.80 b
41、ut lessthan 1.00The basing of conclusions on differences in which less than90 % confidence can be placed is not recommended.9. Precision and Bias9.1 The precision and bias of this method are beingdeveloped.ASTM International takes no position respecting the validity of any patent rights asserted in
42、connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the res
43、ponsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive caref
44、ul consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International
45、, 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 AS
46、TM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).Dimension in. mmA314 83B118 28.5C18 3.18D14 6.4E1116 17.5F14 6.4G38 9.5H34 19.0I18 3.18J3716 87K34 19.0L516 7.9M158 41.5N12 12.7O258 67P14 6.4Q718 181R 0.060 1.52S 0.003 0.076T614 159FIG. 7 Stainless Steel Specimen Backup PlateC614 107
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