SU1518735A1 - Method of determining cyanates in waste water - Google Patents

Method of determining cyanates in waste water Download PDF

Info

Publication number
SU1518735A1
SU1518735A1 SU874251824A SU4251824A SU1518735A1 SU 1518735 A1 SU1518735 A1 SU 1518735A1 SU 874251824 A SU874251824 A SU 874251824A SU 4251824 A SU4251824 A SU 4251824A SU 1518735 A1 SU1518735 A1 SU 1518735A1
Authority
SU
USSR - Soviet Union
Prior art keywords
cyanates
determining
waste water
solution
detection sensitivity
Prior art date
Application number
SU874251824A
Other languages
Russian (ru)
Inventor
Валентина Ивановна Лях
Надежда Ивановна Курочкина
Original Assignee
Иркутский государственный научно-исследовательский институт редких и цветных металлов
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 Иркутский государственный научно-исследовательский институт редких и цветных металлов filed Critical Иркутский государственный научно-исследовательский институт редких и цветных металлов
Priority to SU874251824A priority Critical patent/SU1518735A1/en
Application granted granted Critical
Publication of SU1518735A1 publication Critical patent/SU1518735A1/en

Links

Abstract

Изобретение относитс  к способам определени  цианатов в сточных водах после обезвреживани  их хлорпродуктами и позвол ет повысить чувствительность определени  в 10 раз. Способ включает введение в анализируемый раствор хлоридно-сол нокислого буфера, соли железа (Ш) и последующее фотометрирование раствора. Чувствительность определени  20 мг/л.The invention relates to methods for the determination of cyanates in wastewater after their disposal by chlorine products and makes it possible to increase the detection sensitivity by a factor of 10. The method includes the introduction of chloride hydrochloride buffer, iron salt (III) into the analyzed solution and the subsequent photometry of the solution. Detection sensitivity 20 mg / l.

Description

Изобретение относитс  к аналити- : ческой химии и может быть использовано при анализе сточных вод после обезвреживани  в них цианидов хлор- продуктами, а также в различных технологических исследовани х дл  контрол  за ходом обезвреживани .The invention relates to analytical and chemical chemistry and can be used in the analysis of wastewater after the neutralization of cyanide in them with chlorine products, as well as in various technological studies to monitor the progress of neutralization.

Цель изобретени  - повышение чувствительности анализа.The purpose of the invention is to increase the sensitivity of the analysis.

Пример. В мерные колбы вместимостью 50 мл внос т 20 мл анализируемой сточной воды. Добавл ют 1 мл буферного раствора, содержащего в 1 л 250 мл 0,2 М раствора хлорида кали , 33,5 мл раствора сол ной кислоты с концентрацией 0,2 М, довод т до метки, перемешивают и через 20 мин измер ют оптическую плотность в кювете 10 мм, примен   светофильтр с областью пропускани  ОО им.Example. 20 ml of the analyzed waste water is introduced into 50 ml volumetric flasks. 1 ml of a buffer solution containing 250 ml of a 0.2 M potassium chloride solution in 1 liter, 33.5 ml of a 0.2 M hydrochloric acid solution is added to 1 liter, made up to the mark, mixed and after 20 min the optical density in a cuvette of 10 mm, using a filter with a transmission area of the OO im.

В воде обнаружено 38,0 мг/л циа- нов (введено А2,0 мг/л). Известным38.0 mg / l of cyans was detected in water (A2.0 mg / l was introduced). Famous

способом определить цианат-ионы невозможно из-за недостаточной чувствительности способа.the way to determine cyanate ions is impossible due to the lack of sensitivity of the method.

Хлоридно-сол но-кислый буферный раствор преп тствует образованию осадка гидроксида железа.The hydrochloric acid buffer solution prevents the formation of iron hydroxide precipitate.

Чувствительность определени  20 мг/л. Чувствительность определени  в известном способе 200 мг/л, .Detection sensitivity 20 mg / l. The sensitivity of the determination in the known method is 200 mg / l,.

Claims (1)

Формула изобретени .Claims. Способ определени  цианатов в сточных водах после обезвреживани  их хлорпродуктами, включаюи|ий введение соли металла и последующее фотометрирование раствора, о т л и ч а- ю щ и и с   тем, что, с целью повышени  чувствительности анализа, в анализируемый раствор предварительно ввод т хлоридно-сол но-кислый буфер, а в качестве соли металла используют соль железа (III) .The method for determining cyanates in wastewater after their neutralization with chlorine products, including the introduction of a metal salt and the subsequent photometric measurement of the solution, is about that and, in order to increase the sensitivity of the analysis, chloride-hydrochloric acid buffer, and iron (III) salt is used as the metal salt. (L елate 0000 со СПwith SP
SU874251824A 1987-05-29 1987-05-29 Method of determining cyanates in waste water SU1518735A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU874251824A SU1518735A1 (en) 1987-05-29 1987-05-29 Method of determining cyanates in waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU874251824A SU1518735A1 (en) 1987-05-29 1987-05-29 Method of determining cyanates in waste water

Publications (1)

Publication Number Publication Date
SU1518735A1 true SU1518735A1 (en) 1989-10-30

Family

ID=21306930

Family Applications (1)

Application Number Title Priority Date Filing Date
SU874251824A SU1518735A1 (en) 1987-05-29 1987-05-29 Method of determining cyanates in waste water

Country Status (1)

Country Link
SU (1) SU1518735A1 (en)

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Лурье Ю.Ю. Аналитическа хими промышленных сточных вод. М,: Хими , 198 с.96-98. Авторское свидетельство СССР ff 570821, кл. G 01 N 21/43, 1977. *

Similar Documents

Publication Publication Date Title
Pai et al. pH and buffering capacity problems involved in the determination of ammonia in saline water using the indophenol blue spectrophotometric method
SU1518735A1 (en) Method of determining cyanates in waste water
Wajon et al. The analysis of free chlorine in the presence of nitrogenous organic compounds
Nusbaum et al. Determination of cyanides in sewage and polluted waters
SU1239563A1 (en) Method of determining triethanolamine in industrial effluent
SU1089514A1 (en) Cyanide determination method
SU1659802A1 (en) Photometric method for determining oxyethylated alkylphenols in mineralized water
SU1684660A1 (en) Method of quantitative determination of thiamine bromide
SU709952A1 (en) Method of spectorphotometric determining of scandium
SU1427253A1 (en) Method of analyzing samarium in gadolinium oxide
SU1059491A1 (en) Tetracyclin determination method
SU1672316A1 (en) Method of determination of penicillin and its derivatives
SU826222A1 (en) Method of quantitative determining of 1,2,3 -benzotrizole
SU1506336A1 (en) Method of analysis of dimaleimides
RU2038584C1 (en) Method of assay of nonionogenic surface-active substances
SU1495717A1 (en) Method for photometric analysis of fluiride ions
RU2125724C1 (en) Method of determining zinc in water
SU1659801A1 (en) Method of photometric determination of lead in bronze
SU661308A1 (en) Method of quantitative determining of oxyethylated surface-active substancies
SU388217A1 (en) ALL-UNION
SU1385040A1 (en) Method of determining "thallactam" floto-reagent based on sodium chloride of n-acylated e-amino-caproic acid in aqueous solutions
SU1693491A1 (en) Method of quantitative determination of antimony
SU951127A1 (en) Perflourvalerian acid determination method
SU1686346A1 (en) Method for quantitative estimation of azathioprine
SU1293648A1 (en) Method of determining ferric iron in presence of oxyethylene-diphosphoric acid