SU121450A1 - The method of obtaining nitrilotriacetic acid - Google Patents

The method of obtaining nitrilotriacetic acid

Info

Publication number
SU121450A1
SU121450A1 SU605656A SU605656A SU121450A1 SU 121450 A1 SU121450 A1 SU 121450A1 SU 605656 A SU605656 A SU 605656A SU 605656 A SU605656 A SU 605656A SU 121450 A1 SU121450 A1 SU 121450A1
Authority
SU
USSR - Soviet Union
Prior art keywords
obtaining
nitrilotriacetic acid
acid
reagents
ammonium carbonate
Prior art date
Application number
SU605656A
Other languages
Russian (ru)
Inventor
Л.П. Ревякина
кина Л.П. Рев
Л.С. Троянкер
нкер Л.С. Тро
Original Assignee
Л.П. Ревякина
кина Л.П. Рев
Л.С. Троянкер
нкер Л.С. Тро
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 Л.П. Ревякина, кина Л.П. Рев, Л.С. Троянкер, нкер Л.С. Тро filed Critical Л.П. Ревякина
Priority to SU605656A priority Critical patent/SU121450A1/en
Application granted granted Critical
Publication of SU121450A1 publication Critical patent/SU121450A1/en

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Нитрилотриуксусна  кислота, известна  также под названием «комплексон I, примен етс  в качестве реактива в аналитической химии и дл  разделени  цериевой групны редкоземельных элементов как один из наиболее эффективных сорбентов.Nitrilotriacetic acid, also known as "complexone I," is used as a reagent in analytical chemistry and for the separation of the cerium group of rare-earth elements as one of the most effective sorbents.

В литературе описан одностадийный способ получени  указанной кислоты, заключаюи1ийс  во взаимодействии монохлоруксусной кислоты с углекислым аммоние. в водной среде в присутствии едкой щелочи. При этом процесс ведут при нагревашш с загрузкой реагентов по част м, что усложн ет работу в производственных услови х.The literature describes a one-step process for the preparation of this acid, concluded in the interaction of monochloroacetic acid with ammonium carbonate. in aqueous medium in the presence of caustic alkali. In this case, the process is carried out at heating with the loading of reagents in parts, which complicates the work under production conditions.

Дл  устранени  указанного недостатка предлагаетс  вводить все реагенты в реактор в один прием одновременно, что позвол ет ускорить процесс и проводить его без подвода тепла извне.To eliminate this drawback, it is proposed to introduce all reagents into the reactor in one step at a time, which allows speeding up the process and carrying out it without heat supply from the outside.

Пример. К раствору 2 кг углекислого аммони  в 2 л воды добавл ют 3,2 кг монохлоруксусной кислоты и 10 л раствора едкого кали уд. в. 1,24 и оставл ют на 18-20 час. После этого реакционную массу фильтруют и фильтрат обрабатывают концентрированной сол ной кис .лотой ,5-2,0. В результате выдел етс  нитрнлотриуксусна  кислота , выход которой колеблетс  в пределах 50-55% к теории.Example. To a solution of 2 kg of ammonium carbonate in 2 liters of water is added 3.2 kg of monochloroacetic acid and 10 liters of potassium hydroxide solution. at. 1.24 and left for 18-20 hours. After that, the reaction mass is filtered and the filtrate is treated with concentrated hydrochloric acid, 5-2.0. As a result, nitrochlorotriacetic acid is released, the output of which ranges from 50-55% of theory.

Предмет изобретени Subject invention

Способ получени  питрилотриуксусной кислоты путем взаимодействи  монохлоруксусной кислоты с углекислым аммонием в водной среде в присутствии едкой щелочи, отличающийс  тем, что, с целью ускорени  процесса и возможного проведени  его без подвода тепла извне, все реагенты ввод т в реактор в один прием одновременно.A method of producing pitrilotriacetic acid by reacting monochloroacetic acid with ammonium carbonate in an aqueous medium in the presence of caustic alkali, characterized in that, in order to accelerate the process and possibly conduct it without heat from outside, all reagents are introduced into the reactor at one time.

SU605656A 1958-08-09 1958-08-09 The method of obtaining nitrilotriacetic acid SU121450A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU605656A SU121450A1 (en) 1958-08-09 1958-08-09 The method of obtaining nitrilotriacetic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU605656A SU121450A1 (en) 1958-08-09 1958-08-09 The method of obtaining nitrilotriacetic acid

Publications (1)

Publication Number Publication Date
SU121450A1 true SU121450A1 (en) 1958-11-30

Family

ID=48393235

Family Applications (1)

Application Number Title Priority Date Filing Date
SU605656A SU121450A1 (en) 1958-08-09 1958-08-09 The method of obtaining nitrilotriacetic acid

Country Status (1)

Country Link
SU (1) SU121450A1 (en)

Similar Documents

Publication Publication Date Title
SU121450A1 (en) The method of obtaining nitrilotriacetic acid
GB1108975A (en) New sulphonic acid and process for its production
US2976118A (en) Method of preparing hypophosphites
GB891276A (en) Process for the manufacture of potassium fluoride, hydrogen fluoride and silica from potassium fluosilicate
GB1115592A (en) Process for liberating acrylamide from acrylamide sulphate
SU558925A1 (en) Method for producing diethylamino-oxypropylcellulose
SU345785A1 (en) The method of obtaining salts of dinitro compounds
US2394644A (en) Production of alpha-chloro, betahydroxynitriles
ES434722A1 (en) Process for recovery of cyanuric acid from treated chlorinated mother liquor
US2467442A (en) Process for the production of ketogulonic acid
SU106874A1 (en) The method of obtaining highly concentrated anhydrous calcium chlorate
SU118814A2 (en) The method of alkali regeneration from calcium hydrosilicate compounds
US3000909A (en) Process of preparing butylene oxide from butylene chlorohydrin
US2418753A (en) Explosive purification
US3369860A (en) Process for recovering beryllium values
SU870395A1 (en) Method of producing nitroacetic acid salts
GB1119831A (en) Process for the production of barium hydroxide
SU99479A1 (en) The method of obtaining vitamin B1 by condensation of 2-methyl-4-amino-5-halomethylpyrimidine with 4-methyl-5-beta-hydroxyethyl thiazole
US2349542A (en) Recovery of glue from chrometanned leather
SU144479A1 (en) Method for producing diethylenetriaminepentaacetic acid
ATE7026T1 (en) PROCESS FOR THE PREPARATION OF 4-CHLORO-5-AMINO-2-PHENYL-3(2H)-PYRIDAZINONE BY REACTING 4,5DICHLORO-2-PHENYL-3(2H)-PYRIDAZINONE WITH AMMONIA.
GB653993A (en) Process of producing silicic acid from alkali silicates
US1548345A (en) Process for the recovery of ammonia and other valuable chemicals from waste denitration liquors
SU392682A1 (en)
SU422689A1 (en) METHOD OF OBTAINING SODIUM METASILICATE