SU1184813A1 - Method of producing hexachloride triammonium bismuth (iii) - Google Patents

Method of producing hexachloride triammonium bismuth (iii) Download PDF

Info

Publication number
SU1184813A1
SU1184813A1 SU843733984A SU3733984A SU1184813A1 SU 1184813 A1 SU1184813 A1 SU 1184813A1 SU 843733984 A SU843733984 A SU 843733984A SU 3733984 A SU3733984 A SU 3733984A SU 1184813 A1 SU1184813 A1 SU 1184813A1
Authority
SU
USSR - Soviet Union
Prior art keywords
bismuth
triammonium
hexachloride
producing
iii
Prior art date
Application number
SU843733984A
Other languages
Russian (ru)
Inventor
Лидия Максимовна Волосникова
Хикмат Рахматович Исматов
Original Assignee
Институт Химии Ан Узсср
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Институт Химии Ан Узсср filed Critical Институт Химии Ан Узсср
Priority to SU843733984A priority Critical patent/SU1184813A1/en
Application granted granted Critical
Publication of SU1184813A1 publication Critical patent/SU1184813A1/en

Links

Landscapes

  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

СПОСОБ ПОЛУЧЕНИЯ ТРИАММОНИЙ ВИСМУТ METHOD OF OBTAINING TRIAMMONIUM Bismuth

Description

схsc

4iik4iik

0000

1 111 11

Изобретение относитс  к способам получени  триаммоний висмут (1П)гексахлорида и может быть использовано дл  получени  бескислородных хлорсодержащих соединений висмута, а также в производстве чистых соединений рубрщи  и цези .The invention relates to methods for producing triammonium bismuth (1P) hexachloride and can be used to obtain oxygen-free chlorine-containing bismuth compounds, as well as in the manufacture of pure compounds of rubies and cesium.

Цель изобретени  - повышение выхода и чистоты лродукта и упрощение процесса за счет исключени  операции упаривани  раствора.The purpose of the invention is to increase the yield and purity of the product and simplify the process by eliminating the operation of evaporation of the solution.

Пример 1.К смеси из 100 г трихлорида висмута и 55 г хлористого аммони  добавл ют 37,1 мл воды (исходное мольное соотношение компонентов равно 1:3,2:6,5). Смесь перемешивают при комнатной температуре 4 ч и отфильтровьшают. Получают 53,8 г соли, содержащей 65,7% RiCl, NH4C1 и 74 мл фильтрата, содержащего г/л: BiClj 715,6, М1ЦС1 426,8. Выход соли состабил 34,7%. Состав соли,%: (ЫН4)зВ;С1 99,1;NH4C1 0,9.Example 1. To a mixture of 100 g of bismuth trichloride and 55 g of ammonium chloride, 37.1 ml of water are added (the initial molar ratio of the components is 1: 3.2: 6.5). The mixture is stirred at room temperature for 4 hours and filtered. 53.8 g of salt containing 65.7% of RiCl, NH4C1 and 74 ml of filtrate containing g / l: BiClj 715.6, M1CCl1 426.8 are obtained. The output of salt was sotabil 34.7%. Composition of salt,%: (LH4) ЗВ; С1 99.1; NH4C1 0.9.

П р и м е р 2. К смеси из 100 г BiClj и 55 г добавл ют 50,0 мл (исходное мольное соотно шение компонентов 1:3,2:8,7). Смесь перемешивают при комнатной темпера туре 6 ч. Получают 53,0 г осадка.EXAMPLE 2 To a mixture of 100 g of BiClj and 55 g, 50.0 ml are added (the initial molar ratio of the components is 1: 3.2: 8.7). The mixture is stirred at room temperature for 6 hours. 53.0 g of precipitate are obtained.

4813248132

содержащего 65,9% В,-СЦ и 34% и 84 мл фильтрата, содержащего,г/л: BiClj 716,4, NH4C1 413,7. Выход соли составил 34,2%. Состав соли,%: 5 (NH4)3Bi-Cl 99,14, 0,6.containing 65.9% B, -SC and 34% and 84 ml of filtrate, containing, g / l: BiClj 716.4, NH4C1 413.7. The salt yield was 34.2%. The composition of the salt,%: 5 (NH4) 3Bi-Cl 99.14, 0.6.

ПримерЗ. К смеси из 100 г BtCli и 63,8 г WHyC добавл ют 50 мл . Смесь перемешивают 4 ч при комнатной температуре. Получают 52,3 г осадка, содержащего 66,0% BiCl и 34% и 88 мл раствора , содержащего, г/л: BiCIj 712,2, 433. Выход соли составил 31,2%. Состав соли, %: ( 99,5; jHi,Cl 0,5. Исходное мольNH ClExample 50 ml is added to a mixture of 100 g of BtCli and 63.8 g of WHyC. The mixture is stirred for 4 hours at room temperature. Obtain 52.3 g of sediment containing 66.0% BiCl and 34% and 88 ml of a solution containing, g / l: BiCIj 712.2, 433. The salt yield was 31.2%. Composition of salt,%: (99.5; jHi, Cl 0.5. Initial molNH Cl

Н,0 H, 0

нов соотношение Bid,new Bid ratio,

1 :3,7:8,7. 1: 3.7: 8.7.

Пример4. К смеси из 100 г BiCl,, и.63,8 г добавл ют 38,5 МП HjO. Смесь перемешивают 6 ч при комнатной температуре и отфильтровывают. Получают 74 мл фильрата , содержащего 642,6 г/л BiClj и 427,5 г/л и 81,9 г соли, содержащейу%: В/СЦ 62,8; 37,2. Выход соли составил 50,1%. Состав соли,%:(МН4)5В1С1 4 94,8; NH4C1 5,2. Мольное соотношение исходных компонентов равно 1:3,7:6,5.Example4. To a mixture of 100 g of BiCl, and 63.8 g, 38.5 MP HjO are added. The mixture is stirred for 6 hours at room temperature and filtered. 74 ml of the filtrate are obtained, containing 642.6 g / l of BiClj and 427.5 g / l and 81.9 g of salt containing%: B / SC 62.8; 37.2. Salt yield was 50.1%. Composition of salt,%: (МН4) 5В1С1 4 94.8; NH4C1 5.2. The molar ratio of the starting components is 1: 3.7: 6.5.

Claims (1)

СПОСОБ ПОЛУЧЕНИЯ ТРИАММОНИЙ ВИСМУТ (111) ГЕКСАХЛОРИДА, включающий совместное растворение трихлорида висмута и хлорида аммония в воде и кристаллизацию целевого продукта, отличающийся тем, что, с целью повышения выхода и чистоты целевого продукта и упрощения процесса за счет исключения операции упаривания раствора, исходные компоненты берут в мольном соотношении В1С1Э : NH4C1 : Н^О = 1:3,23,7:6,5-8,7 и процесс ведут при перемешивании в течение 4-6 ч.METHOD FOR PRODUCING BISMUTH (111) TRIAMMONIUM HEXACHLORIDE, comprising co-dissolving bismuth trichloride and ammonium chloride in water and crystallizing the target product, characterized in that, in order to increase the yield and purity of the target product and simplify the process by eliminating the operation of evaporation of the solution, the starting components are taken in a molar ratio of B1C1 E : NH 4 C1: H ^ O = 1: 3.23.7: 6.5-8.7 and the process is carried out with stirring for 4-6 hours СаЭSae 1)81) 8
SU843733984A 1984-04-21 1984-04-21 Method of producing hexachloride triammonium bismuth (iii) SU1184813A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU843733984A SU1184813A1 (en) 1984-04-21 1984-04-21 Method of producing hexachloride triammonium bismuth (iii)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU843733984A SU1184813A1 (en) 1984-04-21 1984-04-21 Method of producing hexachloride triammonium bismuth (iii)

Publications (1)

Publication Number Publication Date
SU1184813A1 true SU1184813A1 (en) 1985-10-15

Family

ID=21116397

Family Applications (1)

Application Number Title Priority Date Filing Date
SU843733984A SU1184813A1 (en) 1984-04-21 1984-04-21 Method of producing hexachloride triammonium bismuth (iii)

Country Status (1)

Country Link
SU (1) SU1184813A1 (en)

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Mel lor J.W, Comprehensive Treatise on Inorganic and Theoretical Chemistry. 1%0, т.9, с.664-665. Там же, с. 666, () *

Similar Documents

Publication Publication Date Title
RU1797607C (en) Process for preparing [@]-@@@-ethyl-2-oxo-1-pyrrolidine acetamide
SU1184813A1 (en) Method of producing hexachloride triammonium bismuth (iii)
US5155257A (en) Process for the preparation of acylaminomethanephosphonic acids
US4622426A (en) Preparation of N,N'-bis(2-hydroxyethyl)oxamide
US4250109A (en) Process for preparing hexamethylene bis-dicyandiamide
KR950005507B1 (en) Process for the preparation of n-(sulfonylmethyl)tormamide
US4668798A (en) Process for preparing pyrrolidine derivatives
CA2000184C (en) Trihydrates of sodium l- and d-2-pyrrolidone-5-carboxylate
US3952011A (en) Process for producing hemi-alkali metal salt of 2-pyrrolidone-5-carboxylic acid
SU1608123A1 (en) Method of producing lead fluorozirconate
SU1168562A1 (en) Method of obtaining 4-(9-acridinyl)pyridilmethane
SU1446111A1 (en) Method of producing barium octafluorozirconate
SU1393791A1 (en) Method of producing potassium nitrate and ammonium chloride
SU570598A1 (en) Method of preparing erythro-and treo-4-hydroxy-di-glutaminic acids
SU1386571A1 (en) Method of producing pentafluorobismuthate (iii) of alkali metals
SU1502465A1 (en) Method of producing crystal strontium diborate
SU391062A1 (en) METHOD OF OBTAINING DOUBLE METAL KANIUM METHANADATE
SU1100228A1 (en) Method of preparing complexes of sulfur trioxide
SU1669867A1 (en) Method for preparation of sodium dithioarsenate
SU1604736A1 (en) Method of producing double tripolyphosphate ammonium-alkali metal
SU1480757A3 (en) Method of producing potassium sulfate
SU433787A1 (en) Method of preparing tetraalkyl(aryl) trithiopyrophosphinates
SU1018908A1 (en) Process for producing titanium iodate
SU1386568A1 (en) Method of producing potassium dithiocyanatediiodidecadmate
US2647894A (en) 2-chloroprocaine salt of penicillin omicron