HG/T 3483-1978 Chemical reagent sodium tetraphenylborate (formerly HG/T 3-1164-78) HG/T3483-1978 standard download decompression password: www.bzxz.net

Ministry of Petrochemical Industry of the People's Republic of China
Chemical Reagents
This reagent is colorless or white crystal, slightly hygroscopic, soluble in water and ethanol. Molecular formula: NaB(C,H,)4
Molecular weight: 342.22 (according to the international atomic weight of 1975) I. Technical conditions
1. NaB(CH,) content not less than:
Analytical pure
Chemical pure
2. Potassium sensitivity test: qualified.
3. Maximum impurity content (indicators in %): name
(1) Clarity test
(2) Acetone solubility test
(3) Drying loss
II. Inspection rules
Sampling and acceptance shall be carried out in accordance with the provisions of GB619-77. 3. Test Methods
HG 3-1164-78
The standard solutions, impurity standard solutions, preparations and products required for the determination shall be prepared in accordance with the provisions of GB601-77, GB602-77 and GB603-77. 1. Determination of NaB(CH4)4 content: Weigh 0.2 g of sample to the nearest 0.0002 g. Dissolve in 100 ml of water, add 1 ml of glacial acetic acid and quickly add 10 ml of 3% potassium nitrate solution under stirring. Keep warm in a 50-55°C water bath for 30 minutes and cool. Place in an ice bath for 30 minutes and filter with a constant weight No. 4 glass filter crucible. Wash the precipitate with 20 ml of clear saturated tetraphenylborate potassium solution four times, and then wash the precipitate with 20 ml of water four times. Bake at 105-110°C to constant weight. The content of NaB(C.Hs)% (X) is calculated according to the following formula: G,×0. 9550×100
Wherein: --sample weight, g;
G.\-precipitate weight, g;
0.9550--coefficient of converting KB(CH,)4 into NaB(C.Hs) Issued by the Ministry of Petrochemical Industry of the People's Republic of China
Shaanxi Petroleum Industry Bureau
October 1, 1978
Xi'an Chemical Reagent Factory
HG 3-1164-78
2. Potassium chlorination test: Weigh 3.42 grams of sample and dissolve it in 100 ml of water (solution 1). Take 0, 0.005, 0.010.015 mg of K and 1 drop of 30% acetic acid respectively, dilute to 3 ml, add 1 ml of "solution I", shake, let stand for 5 minutes, and compare with the blank. There should be a clear difference in turbidity.
3. Impurity determination: The sample must be weighed to 0.01 g. (1) Clarity test: Weigh 0.5 g of sample, weigh to 0.01 g, and dissolve in 100 ml of ammonia-free water. The clarity should not be greater than the clarity standard:
Analytical pure
No. 3; bZxz.net
: No. 5.
Chemical pure
(2) Acetone solubility test: Weigh 0.2 g of sample and dissolve in 5 ml of acetone. The solution should be clear and free of mechanical impurities. (3) Loss on drying: Weigh 1 g of sample, place in a constant-weight weighing bottle, and weigh to 0.0002 g. Dry at 105-110℃ until the weight is reduced, and calculate the weight loss percentage from the reduced weight. IV. Packaging and marking
1. Packaging: in accordance with the provisions of HG3-119-64. Inner packaging form: Gz-2;
Outer packaging form: 1-1, I, Zui;
Packing unit: Class 2.
2. Marking: in accordance with the provisions of HG3-119--64. 1279
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