ISO 6995-1985 Aluminium ores Determination of titanium content 4 4--Diantipyrylmethane spectrophotometric method《铝土矿石 钛含量的测定 4 4--二安替吡啉甲烷分光光度法》.pdf

《ISO 6995-1985 Aluminium ores Determination of titanium content 4 4--Diantipyrylmethane spectrophotometric method《铝土矿石 钛含量的测定 4 4--二安替吡啉甲烷分光光度法》.pdf》由会员分享，可在线阅读，更多相关《ISO 6995-1985 Aluminium ores Determination of titanium content 4 4--Diantipyrylmethane spectrophotometric method《铝土矿石 钛含量的测定 4 4--二安替吡啉甲烷分光光度法》.pdf（7页珍藏版）》请在麦多课文档分享上搜索。

1、International Standard 6995 0 * 4 4J!gi!b INTERNATIONAL ORGANIZATION FOR STANDARDlZATlON.MEXWHAPOAHAR OPI-AHMBAUMR fl0 CTAHAAPTM3ALWWORGANlSATlON INTERNATIONALE DE NORMALISATION Aluminium ores - Determination of titanium content - 4,4-Diantipyrylmethane spectrophotometric method Minerais alumineux -

2、. Dosage du titane - M or or b) Sintering with sodium peroxide followed by a brief fusion. Dissolution of the melt with sulfuric acid. NOTE - This method is recommended for ores containing diaspore and when the residue after silica volatilization for acid decomposition is greater than 1 % of the mas

3、s of the test portion; c) Fusion with sodium tetraborate/sodium carbonate flux followed by treatment with sulfuric acid. NOTE - This method is suitable for all types of ores. Dehydration of silica, dissolution of salts, and filtration and ignition of the residue. Removal of the silica by evaporation

4、 with hydrofluoric and sulfuric acids. Fusion of the residue with sodium carbonate/sodium tetraborate flux, dissolution of the melt with sulfuric acid and addition to the main solution. Reduction of the iron with ascorbic acid; colour development with 4,4-diantipyrylmethane and measurement of the ab

5、sor- bance at about 390 nm. 4 Reagents During the analysis, use only reagents of analytical reagent grade and only distilled water or water of equivalent purity. 4.1 Sodium peroxide. NOTE - Sodium peroxide should be protected against humidity and should not be used once it has begun to agglomerate.

6、4.2 Sodium carbonate/sodium tetraborate flux. Mix 3 parts by mass of anhydrous sodium carbonate and 1 part by mass of anhydrous sodium tetraborate. 4.3 Hydrofluoric acid, 40 % (m/m), Q I,13 g/ml. 4.4 Sulfuric acid, em I,84 g/ml, diluted 1 + 1. 4.5 Sulfuricacid, em I,84 g/ml, diluted 1 + 9. 4.6 Hydro

7、chloric acid, 20 I,17 g/ml, diluted 1 + 1. 4.7 Acid mixture. Measure into a one-litre beaker 225 ml of water and add cautiously, with mixing, 175 ml of sulfuric acid (em I,84 g/ml). Cool to room temperature and add 150 ml of hydrochloric acid (em I,17 g/ml) and 50 ml of nitric acid (em I,42 g/ml). P

8、repare this solution fresh for each series of determinations and discard any unused solution. 4.8 Ascorbic acid, 100 g/l solution. Prepare this solution as required. 4.9 4,4-Diantipyrylmethane, 15 g/l solution. Dissolve 15 g of 4,4-diantipyrylmethane (C2sH24N402) in 1 I of sulfuric acid solution (em

9、 I,84 g/ml, diluted 1 + 49). Prepare fresh as required. 4.10 Ammonium iron(lll) sulfate solution. Dissolve 6 g of ammonium ironfIll) sulfate - 24 water Fez(NH4)2(S04)4.24H201 in 1 litre of water containing 10 ml of the sulfuric acid solution (4.5). 1 Copyright International Organization for Standard

10、ization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-IS0 69951965 (E) 4,ll Titanium, standard solution, corresponding to I,0 g of TiOz per litre. One of the following methods may be used : a) Weigh, to the nearest 0,001 g, 0

11、,300 g of high purity (99,9 %I titanium metal into a conical flask, add 50 ml of water and 50 ml of the sulfuric acid solution (4.4) and heat to dissolve the metal. Oxidize the solution until the purple colour disappears by adding, drop by drop, nitric acid solution (20 1,42 g/ml, diluted 1 + 4). Co

12、ol and transfer quantitatively to a 500 ml one-mark volumetric flask. Dilute to the mark and mix thoroughly. b) Weigh, to the nearest 0,001 g, 0,500 g of high purity (99,9 %I titanium dioxide (previously ignited in a platinum crucible at 950 to 1 000 OC for 30 min and dried at 105 rt 5 OC) into a 25

13、0 ml conical flask. Add 8 g of am- monium sulfate and 25 ml of sulfuric acid (em 1,84 g/ml). Insert a short-stemmed glass funnel in the neck of the flask and heat cautiously with frequent agitation to incipient boiling. Continue heating until complete dissolution has been effected and no unattacked

14、material remains on the walls of the flask. Cool to ambient temperature and add 200 ml of cold water in one portion without mixing. Mix when the addition is complete, cool, transfer quan- titatively to a 500 ml one-mark volumetric flask using 100 ml of the sulfuric acid solution (4.5) and dilute to

15、the mark with water. NOTE - When using a hot-plate, ensure that it is at maximum temperature so that incipient boiling is reached in the minimum time. c) Weigh, to the nearest 0,001 g, 2,215 g of potassium titanium oxalate dihydrate K2TiO(C204)2.2H201 into a 250 ml conical flask; add 25 ml of sulfur

16、ic acid ( I,84 g/ml) and gradually heat to boiling. Boil for 10 min, cool well and pour the solution into 300 to 400 ml of water. Cool and transfer quantitatively to a 500 ml one-mark volumetric flask. Dilute to the mark and mix thoroughly. 4.12 Titanlum, standard solution corresponding to 25 mg of

17、TiOP per litre. Pipette 5,0 ml of the standard titanium solution (4.11) into a 200 ml one-mark volumetric flask, dilute to the mark with the sulfuric acid solution (4.5) and mix thoroughly. Prepare this solution immediately before use. 5 Apparatus Ordinary laboratory glassware and apparatus, and 51

18、Muffle furnaces, adjustable from 480 OC to greater than 1 ooo oc. 5.2 Zirconium crucibles, approximately 40 ml capacity, for sinter decomposition. 5.3 Platinum/gold alloy (95/51 crucibles or equivalent, approximately 25 ml capacity, for the fusion decomposition in 7.5.1.3. 5.4 Platinum crucibles, fo

19、r treatment of the residue in 7.5.3. 5.5 Spectrophotometer, suitable for measurement of absorbance at about 390 nm. 5.5 Desiccator, containing phosphorus(V) oxide as desic- cant. 6 Sampling and preparation of samples Laboratory samples shall be taken and crushed to pass a 150 urn test sieve, in acco

20、rdance with the methods specified in the ielevant standards 1. 7 Procedure 7.1 Number of determinations Carry out the analysis in duplicate and ore sample. independently on each NOTE - The expression “independently” implies a change of the person carrying out the analysis. If the same person must ca

21、rry out the analysis, the procedure shall be carried out at different times. 7.2 Test portion Weigh, to the nearest 0,000 1 g, approximately 1 g of test sample. 7.3 Blank test In parallel with the decomposition of the test portion, prepare a blank solution according to the method of decomposition, b

22、ut omitting the test portion. When the analysis is carried out on several samples at the same time, the blank value may be represented by one test, provided that the procedure is the same and the reagents used are from the same bottles. 7.4 Check test In each run, one analysis of a certified referen

23、ce material of the same type of ore shall be carried out in parallel, and under the same conditions, with the analysis of one ore sample. NOTE - The certified reference material should be of the same type as the sample to be analysed. Such certified reference material cannot, however, be considered

24、as being of the same type if the properties of 1) Where no International Standards exist, the relevant standards shall be the national standards. Two International Standards on this subject are currently in preparation : IS0 6137, Aluminium ores - Method of sampling, and IS0 6140, Aluminium ores - P

25、reparation of samples. 2 Copyright International Organization for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-IS0 6995-1965 (El the sample to be analysed differ from those of the certified reference material

26、 to such an extent that the analytical procedure must be changed substantially. 7.5 Determination 7.5.1 Decomposition of the test portion If the decomposition is to be based on acid attack, proceed as specified in 7.5.1 .I. If the decomposition is to be based on alkali sintering, proceed as specifie

27、d in 7.5.1.2. If the decom- position is to be based on fusion, proceed as specified in 7.5.1.3. 7.5.1.1 Acid decomposition Transfer the test portion (7.2) to a 400 ml beaker. Moisten with water and add 60 ml of the acid mixture (4.7). Cover the beaker and heat at 80 X to decompose the sample. NOTE -

28、 With samples of high iron content 15 % (m/ml of Fe,O,l, the initial heating should be conducted for an extended period. When the evolution of brown fumes ceases, carefully rinse the cover and wall of the beaker, Evaporate the uncovered solution to dense fumes of sulfuric acid. Replace the cover and

29、 heat strongly for 50 min on a hot-plate set to produce in the solution a temperature of 210 I!I 10 OC. NOTE - Determine the temperature setting by using a separate test beaker containing a partial-immersjon thermometer in a 10 mm depth of sulfuric acid. 7.5.1.2 Alkali sinter decomposition Transfer

30、the test portion (7.2) to a dry zirconium crucible (5.21, add 10 g of the sodium peroxide (4.1) and mix intimately using a dry metal spatula. Place the crucible and contents in a muffle furnace (5.1), maintained at490 to 500 OC, for45 min. Remove the crucible and contents from the furnace and heat o

31、ver a burner to melt the sinter (about 30 s). Continue heating the melt while swirling for a total time of 2 min. Allow the crucible to cool to ambient temperature (a metal block can be used to expedite this process) and place it on its side in a 400 ml beaker. Cover and add cautiously at the rear o

32、f the crucible 140 ml of the sulfuric acid solution (4.5). Add 20 ml of the sulfuric acid solution (4.4) and digest to leach the con- tents of the crucible. Remove the crucible when the contents are completely leached and rinse well into the solution in the beaker. Carefully rinse the cover and wall

33、 of the beaker. Evaporate the uncovered solution to dense fumes of sulfuric acid. Replace the cover and heat strongly for 50 min on a hot-plate set to produce in the solution a temperature of 210 + 10 OC. 7.5.1.3 Fusion decomposition Transfer the test portion (7.2) to a dry platinum/gold crucible (5

34、.3, see the note), add 2 g of the sodium carbonate/sodium tetraborate flux (4.2) and mix intimately using a dry metal spatula. Cover with a platinum lid and place in a muffle furnace (5.11, maintained at 480 to 500 OC, for 5 min, then transfer to a muffle furnace, maintained at 900 to 950 OC, for 10

35、 min. NOTE - A platinum crucible may be used, but care should be taken to ensure that the hot fusion mixture does not “creep” over the side of the crucible. Consequently, it would be preferable to use a larger platinum crucible, e.g. 30 ml. Allow the crucible to cool and place it on its side in a 40

36、0 ml beaker. Add 40 ml of water and 35 ml of the sulfuric acid solution (4.41, cover and digest to leach the contents of the crucible. Remove the crucible when the contents are com- pletely leached and rinse well into the main solution. Carefully rinse the cover and wall of the beaker. Evaporate the

37、 uncovered solu$on to dense fumes of sulfuric acid. Replace the cover and heat strongly for 50 min on a hot-plate set to produce in the solution a temperature of 210 f 10 OC 7.5.2 Dissolution and filtration Cool the solution from 7.5.1.1, 7.5.1.2 or 7.5.1.3 to ambient temperature, cautiously add 130

38、 ml of water and heat to 80 to 90 OC for at least 40 min. with stirring, to completely dissolve the salts. Filter while hot through a medium-texture filter paper, collecting the filtrate in a 250 ml one-mark volumetric flask. Rinse the beaker with water and, using a rubber-tipped glass rod, clean th

39、e beaker and transfer the residue quantitatively to the paper. Wash the paper and residue five times with 5 to 10 ml aliquot portions of hot water. Reserve the filtrate and washings for use in 7.5.3. Retain the filter paper and residue and continue according to 7.5.3. NOTE - With high titanium conte

40、nts, it may be necessary to increase the volume of wash solution. 7.5.3 Treatment of the residue Transfer the filter paper and residue from 7.5.2 to a pre-ignited tared platinum crucible (5.4). Dry and char slowly and then ash the filter paper by increasing the temperature to 500 to 700 OC for 30 mi

41、n in a muffle furnace (5.1). Allow the crucible to cool and moisten the residue with a few drops of water. Add 5 drops of the sulfuric acid solution (4.4) and, depending on the silica content, 5 to 15 ml of the hydrofluoric acid (4.3). Evapor- ate carefully to dryness in a fume cupboard to expel sil

42、ica and sulfuric acid. Allow the crucible to cool, and weigh. Determine the mass of residue to ensure that the conditions of clause 3 are met. Add 0,7 + 0,l g of the flux (4.2). Fuse at above 1 000 OC for 4 to 5 min in a muffle furnace (5.11, roll the melt briefly, then return to the furnace for 1 t

43、o 2 min. Allow the crucible to cool, add IO ml of the sulfuric acid solution (4.5) and warm to dissolve the fused mass. Transfer the solution to the reserved filtrate (7.5.21, rinsing the crucible with water. Cool to ambient temperature, dilute to the mark with water and mix. Prepare test solutions

44、in accordance with table 1. Table 1 - Intermediate dilutions I TiO, content I Volume of aliquot portion Final volume I I % hlml I ml I ml I 0.5 to 2,0 25,00 5% 2,0 to 4.0 25,00 100,OO 4.0 to 8.0 25.00 200.00 3 Copyright International Organization for Standardization Provided by IHS under license wit

45、h ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-IS0 69951985 (El 7.6.4 Spectrophotometric determination Pipette a 5 ml aliquot portion of the test solution or diluted test solution, prepared in accordance with 7.5.3, and of the blank test solution, prepared si

46、milarly, into separate 50 ml one-mark volumetric flasks. Add 5 ml of the ammonium ironfIll) sulfate solution (4.101 to each flask. Add 5 ml of the ascorbic acid solution (4.81, mix and allow to stand for 10 min. Add 10 ml of the hydrochloric acid solution (4.61, mix well, then add 15 ml of the 4,4-d

47、iantipyrylmethane solution (4.9). Dilute to the mark and mix. Allow to stand for 60 min and measure at the peak absorbance at about 390 nm in a 10 mm cell using water as the reference solution. 7.6 Calibration graph Pipette aliquot portions of the standard titanium solution (4.12) as shown in table

48、2 into separate 50 ml one-mark volumetric flasks. Add 5 ml of the ammonium iron(lll1 sulfate solution (4.101,5 ml of the ascorbic acid solution (4.81, mix and allow to stand for 10 min. Add 10 ml of the hydrochloric acid solution (4.61, mix well, then add 15 ml of the 4,4-diantipyrylmethane solution

49、 (4.9). Dilute to the mark and mix. Table 2 - Mass of TiO2 in titanium solutions Volume of standard titanium solution (4.12) ml Mass of TiO, I4 0,o 0 2,o 50 48 100 60 150 80 200 Allow to stand for 60 min and measure at the peak absorbance at about 390 nm In a 10 mm cell using water as the reference solution. Plot the absorbance of each calibration solution against the quantity of titanium dioxide, in micrograms. 8 Expression of results 8.1 Calculation of titanium dioxide content The titanium content, expressed as a