
GB/T 4375.6-1984 Chemical analysis methods for gallium - Salicylfluorone-cetyltrimethylammonium bromide spectrophotometric method for the determination of tin content
time:
2024-08-04 11:20:17
- GB/T 4375.6-1984
- Abolished
Standard ID:
GB/T 4375.6-1984
Standard Name:
Chemical analysis methods for gallium - Salicylfluorone-cetyltrimethylammonium bromide spectrophotometric method for the determination of tin content
Chinese Name:
镓化学分析方法 水杨基荧光酮-溴化十六烷基三甲基铵光度法测定锡量
Standard category:
National Standard (GB)
-
Date of Release:
1984-04-30 -
Date of Implementation:
1985-04-01 -
Date of Expiration:
2007-09-29
Standard ICS number:
Metallurgy>>Non-ferrous metals>>77.120.70 Cadmium, cobalt and their alloysChina Standard Classification Number:
Metallurgy>>Metal Chemical Analysis Methods>>H14 Analysis Methods for Rare Metals and Their Alloys
alternative situation:
Adjusted to YS/T 520.6-2006
Review date:
2004-10-14Drafting Organization:
Nonferrous Metals Research InstituteFocal point Organization:
National Technical Committee for Standardization of Nonferrous MetalsPublishing Department:
China Nonferrous Metals Industry AssociationCompetent Authority:
China Nonferrous Metals Industry Association

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Summary:
GB/T 4375.6-1984 Chemical analysis method for gallium - Determination of tin content by salicylfluorone-cetyltrimethylammonium bromide spectrophotometry GB/T4375.6-1984 standard download decompression password: www.bzxz.net

Some standard content:
National Standard of the People's Republic of China
Methods for chenigal analysis of gallium The salicylfinorone cetyltrlmethylanmonipnbroinide photometric method forLhe determlnatiou of thn couteut Standard: GB/T69.871:54a.42-5.86.811.811 GB43T5.6-04 This cup god 78 "Gold product chemical protection and shares. ■ Method tips
The sample is acid. Please make sure that the acid is pure. It is allowed to add N carbonate to the chemical to avoid differentiation: use with plastic and original shape. To resist the potential horse Xie, there are 2 tax belt tour, let: for the standard chemical system, money this field to mention the light heart - dilute! People burn card a volume according to the shape of the yellow compound, very complete determination of the firm plan war wind rm place monitoring head light. 2 reagents
2.2 elimination line, superior grade clock (ratio city 1.42): 2.3 before acid, Ji (!: 1)
z.4 class, ratio absorption (, + 24),
2.5 Australia chemical escort business (30%).
. Ascorbic acid nourishing [].
2-T tartaric acid soluble by 42 (0!)
28): called water or light fall in m (2)
1, month small light full l,! Called in, service.
2.9 stimulate ten models "gated version, account", 32g chemical ten cultivation among them, with the solution of the T group system, 2.10 creation standard production, collection g mirror (, 9 "), the first down 0m burn, people 50 fall (three 1 &), hot grid, cold. Acid (1+4 "will be the liquid like 100 guest he Dan lung release to, mixed, this reverse gain |mlL.iing thank,
1.11 steamed bun standard thick add, and 200ml% storage (.10, 25ml capacity version, Sichuan with the war <1+40) group to,. 1100,
2.12 weak standard drop report: net share 25.00ml said half year (2.1t) in 2%ml wear bottle 1, reward <1+49) release suddenly high,. Narrow liquid! n containing code.
Ben Guangguang determined,
National Standard 1914-04-30 issued
1885.04-1 purchase certificate
4 analysis steps cumulative
industry number rack
r043756-84
weigh the table two upward test samples gradually determined, with average quality, 4.2 test samples
according to the soft clothing, take the reduction selection
5.00003.000.1
.0.002UC.025
empty self-test
follow the previous sample to do three tests.
TKAN KA
Suffer, this standard
4.4.1 put the test mixture (4.2) into 50ml of water, add 2.2ml of 5ml of sodium sulphate, 2.31ml of acid, and wait for the reaction to stop, heat, sulfur, cool. Jiang surface blood and people, buy swimming salts, cool.
1.4,2 month 1l carbon aldehyde (2.3) will be washed with 6ml of condensate fractions into a bucket, and then washed with a little blood water + flow filtration to obtain a product greater than, K ~, when the liquid containing can be added to the GC; H full scale, the fraction rate of 1ml liquid, set the "ml micro-full", add 11ml with aldehyde (2.3)), the micro-fluid is about 26ml, add 4 ml with potassium chloride (2,53, standard, can add 15m benzene [2.1), long simmer for 2 min, simmer, and pass through ice. There are 10m (2.4), swaying m, high fraction. 44. The sample was transferred to a 25-well plate and washed with water. Then, 2.5 ml of concentrated acid solution (2.8) and 1.5 ml of fluorescein solution (2.6) were added to the concentrated solution. The sample was placed in a water-cooled chamber for 3 lmin.
4.4.4 The sample was separated by 1e (1g was used for the test. The absorbance at m was measured by spectrophotometer. The upper curve was 4.6 for the effective preparation.
4 .5.1 Grid connection.0.29..43.0.6f, 0.80a or, 0.05, 0.1.U.15,.2uml standard (2.12) respectively place two 2 yuan ml colorimetric pieces, 1 person 3ml carbon energy (2.3), dilute to 1ml, with a 4.4. item with t.5ml anti-blood ether dye (2.5) of the meter
45.2 transfer part of the full (4..)" 1m3emi, with sample, 1 minute, suction speed, with the whole, standardbzxZ.net
6 minutes expansion result of the meter
according to the formula of the image after the minute also
formula, twist
GH 4375.6-B4
1As a result of the above analysis, the results are shown in Table 2. Table 2
0.otoc5 ~3.02t1
-1.4+? ~ 1.11121
1..42: ~1.1.05
, -,08r:
. -6, UJ8 1. 0212
Additional remarks:
This standard is issued by the State-owned Industrial Corporation. This standard is issued by China National Nonferrous Metals Corporation, which has completed the research and development of nonferrous metals since 2001. This standard must be certified by the National Nonferrous Metals Corporation.
0,14:98
Tip: This standard content only shows part of the intercepted content of the complete standard. If you need the complete standard, please go to the top to download the complete standard document for free.
Methods for chenigal analysis of gallium The salicylfinorone cetyltrlmethylanmonipnbroinide photometric method forLhe determlnatiou of thn couteut Standard: GB/T69.871:54a.42-5.86.811.811 GB43T5.6-04 This cup god 78 "Gold product chemical protection and shares. ■ Method tips
The sample is acid. Please make sure that the acid is pure. It is allowed to add N carbonate to the chemical to avoid differentiation: use with plastic and original shape. To resist the potential horse Xie, there are 2 tax belt tour, let: for the standard chemical system, money this field to mention the light heart - dilute! People burn card a volume according to the shape of the yellow compound, very complete determination of the firm plan war wind rm place monitoring head light. 2 reagents
2.2 elimination line, superior grade clock (ratio city 1.42): 2.3 before acid, Ji (!: 1)
z.4 class, ratio absorption (, + 24),
2.5 Australia chemical escort business (30%).
. Ascorbic acid nourishing [].
2-T tartaric acid soluble by 42 (0!)
28): called water or light fall in m (2)
1, month small light full l,! Called in, service.
2.9 stimulate ten models "gated version, account", 32g chemical ten cultivation among them, with the solution of the T group system, 2.10 creation standard production, collection g mirror (, 9 "), the first down 0m burn, people 50 fall (three 1 &), hot grid, cold. Acid (1+4 "will be the liquid like 100 guest he Dan lung release to, mixed, this reverse gain |mlL.iing thank,
1.11 steamed bun standard thick add, and 200ml% storage (.10, 25ml capacity version, Sichuan with the war <1+40) group to,. 1100,
2.12 weak standard drop report: net share 25.00ml said half year (2.1t) in 2%ml wear bottle 1, reward <1+49) release suddenly high,. Narrow liquid! n containing code.
Ben Guangguang determined,
National Standard 1914-04-30 issued
1885.04-1 purchase certificate
4 analysis steps cumulative
industry number rack
r043756-84
weigh the table two upward test samples gradually determined, with average quality, 4.2 test samples
according to the soft clothing, take the reduction selection
5.00003.000.1
.0.002UC.025
empty self-test
follow the previous sample to do three tests.
TKAN KA
Suffer, this standard
4.4.1 put the test mixture (4.2) into 50ml of water, add 2.2ml of 5ml of sodium sulphate, 2.31ml of acid, and wait for the reaction to stop, heat, sulfur, cool. Jiang surface blood and people, buy swimming salts, cool.
1.4,2 month 1l carbon aldehyde (2.3) will be washed with 6ml of condensate fractions into a bucket, and then washed with a little blood water + flow filtration to obtain a product greater than, K ~, when the liquid containing can be added to the GC; H full scale, the fraction rate of 1ml liquid, set the "ml micro-full", add 11ml with aldehyde (2.3)), the micro-fluid is about 26ml, add 4 ml with potassium chloride (2,53, standard, can add 15m benzene [2.1), long simmer for 2 min, simmer, and pass through ice. There are 10m (2.4), swaying m, high fraction. 44. The sample was transferred to a 25-well plate and washed with water. Then, 2.5 ml of concentrated acid solution (2.8) and 1.5 ml of fluorescein solution (2.6) were added to the concentrated solution. The sample was placed in a water-cooled chamber for 3 lmin.
4.4.4 The sample was separated by 1e (1g was used for the test. The absorbance at m was measured by spectrophotometer. The upper curve was 4.6 for the effective preparation.
4 .5.1 Grid connection.0.29..43.0.6f, 0.80a or, 0.05, 0.1.U.15,.2uml standard (2.12) respectively place two 2 yuan ml colorimetric pieces, 1 person 3ml carbon energy (2.3), dilute to 1ml, with a 4.4. item with t.5ml anti-blood ether dye (2.5) of the meter
45.2 transfer part of the full (4..)" 1m3emi, with sample, 1 minute, suction speed, with the whole, standardbzxZ.net
6 minutes expansion result of the meter
according to the formula of the image after the minute also
formula, twist
GH 4375.6-B4
1As a result of the above analysis, the results are shown in Table 2. Table 2
0.otoc5 ~3.02t1
-1.4+? ~ 1.11121
1..42: ~1.1.05
, -,08r:
. -6, UJ8 1. 0212
Additional remarks:
This standard is issued by the State-owned Industrial Corporation. This standard is issued by China National Nonferrous Metals Corporation, which has completed the research and development of nonferrous metals since 2001. This standard must be certified by the National Nonferrous Metals Corporation.
0,14:98
Tip: This standard content only shows part of the intercepted content of the complete standard. If you need the complete standard, please go to the top to download the complete standard document for free.
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