SU1451590A1 - Method of quantitative analysis of polyacrylamide and polyacrylonitril in aqueous solutions - Google Patents
Method of quantitative analysis of polyacrylamide and polyacrylonitril in aqueous solutions Download PDFInfo
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- SU1451590A1 SU1451590A1 SU864143688A SU4143688A SU1451590A1 SU 1451590 A1 SU1451590 A1 SU 1451590A1 SU 864143688 A SU864143688 A SU 864143688A SU 4143688 A SU4143688 A SU 4143688A SU 1451590 A1 SU1451590 A1 SU 1451590A1
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- USSR - Soviet Union
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- polyacrylamide
- aqueous solutions
- complexing agent
- polyacrylonitril
- quantitative analysis
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Abstract
Изобретение относитс к аналитической химии и может быть использовано в нефтегазодобывакщей целлюлозно-бумажной промьшшенности, в ком мунальном хоз йстве и др. област х дл количественного определени поли акрил амид а и полиакрилонитрила в водных средах, не содержащих галогены . Изобретение позвол ет сократить продолжительность определени с 1- 1,5 ч до 1 мин за счет обработки анализируемой пробы комплексообразую- щим реагентом - нитратом серебра с последуюцим фотоколориметрированием полученной смеси. 1 табл.This invention relates to analytical chemistry and can be used in the oil and gas producing pulp and paper industry, in communal households and other areas for the quantitative determination of poly acrylic amide a and polyacrylonitrile in aqueous media that do not contain halogens. The invention makes it possible to shorten the determination time from 1-1.5 hours to 1 minute by treating the sample being analyzed with a complexing agent, silver nitrate, followed by photocolorimetrication of the mixture obtained. 1 tab.
Description
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Изобретение относитс к аналити- :ческой химии и может быть использова- но в нефтегаЭодобывсиощей, u,ejinrano3но-бумажной промьппленност х, в комму- ; Кельном хоз йстве и других област х 1 дл определени полиакрил амид а(ПАА) I иполиакрилонитрила (ПАН) в водных средах,не содержащих галогены, Целью изобретени вл етс сокра- щение продолжительности определени . Пример, Составл ют рабочую I пробу, содержащую 1 мл 0, I раствора ПАА, 0,5 мл 50%-ного раствора нитрата серебра (реагента) и 3,5 мл воды и холостую пробу, содер- 1 жащую4,5мл ; воды и 0,5 мл 50%-ного раствора нитрата серебра (реагента), I В кюветах толщиной 1 см подвергают колориметрированию на ультрафиоле- товом спектрофотометре УФС), Высота пика полученного спектра при 305 нм составл ет 219 мм. Откладыва эту величину на оси ординат калибровочного графика и провод абсциссу до пересечени с калибровочной пр мой, а из точки пересечени - ординату до пересечени с осью абсцисс, получаем результат анализа: С 0,4997. исчисл ем относительную ошибку ана- ЛИЗ аThe invention relates to analytical: chemical chemistry and can be used in oil and gas production, u, ejinrano3 paper industry, in communi- cation; Cologne and other areas 1 for the determination of polyacrylamide a (PAA) I and polyacrylonitrile (PAN) in aqueous media that do not contain halogens. The aim of the invention is to reduce the duration of the determination. An example is a working sample I, containing 1 ml of 0, I of PAA solution, 0.5 ml of 50% silver nitrate solution (reagent) and 3.5 ml of water and a blank sample containing 1 ml of 4.5 ml; water and 0.5 ml of a 50% silver nitrate solution (reagent), I In cuvettes 1 cm thick, subjected to colorimetry using a UV ultraviolet spectrophotometer), the peak of the obtained spectrum at 305 nm is 219 mm. Putting this value on the ordinate axis of the calibration curve and the abscissa wire to the intersection with the calibration straight line, and from the intersection point to the ordinate to the intersection with the abscissa axis, we obtain the result of the analysis: C 0.4997. calculate relative error ana-LIZ a
jCizC.ioo .(0 000 ; Q |9971.,oo QjCizC.ioo. (0 000; Q | 9971., oo Q
Пример2о Составл ют рабочую пробу, содержащую 1 мл 0,3%-ного раствора ПАА, 5 мл 35%-ного раство- ipa реагента и 3,5 мл воды, и холос- гую пробу, содержащую 0,5 мл 35%-ног реагента и 4,5 мл воды. Пробы подвер гают спектрофотомётрированию на УФС в кюветах толщиной 1 см. ПолученныйExample 2: A sample is made up containing 1 ml of a 0.3% PAA solution, 5 ml of a 35% solution of ipa reagent and 3.5 ml of water, and a hollow sample containing 0.5 ml of a 35% solution. reagent and 4.5 ml of water. Samples are subjected to spectrophotometry on UVC in cuvettes with a thickness of 1 cm.
спектр имеет высоту 197 мм. Найденна по калибровочному графику концентраци растворов ПАА составл ет 0,3015%, относительна ошибка определени 5%.The spectrum has a height of 197 mm. The concentration of PAA solutions found from the calibration graph is 0.3015%, the relative determination error is 5%.
П р и м е р 3. Составл ют рабочую пробу, содержащую 1 мл 0,1%-ного раствора ПАН, 0,1 мл 30%-ного раствора реагента и 3,9 мп воды, и холостую пробу, содержащую 0,1 мл 30%-ного . раствора реагента и 4,9 мл воды. Подвергают колориметрированию на УФС Выысота пика спектра при 305 нм составила 35 мм. Найденна концентраци анализируемого раствора составила 0,0972%, относительна ошибка анализа 2,8%,EXAMPLE 3. A working sample is prepared containing 1 ml of a 0.1% PAN solution, 0.1 ml of a 30% reagent solution and 3.9 ml of water, and a blank containing 0.1 ml of 30%. reagent solution and 4.9 ml of water. Subject to colorimetrication on UFS The height of the peak of the spectrum at 305 nm was 35 mm. The found concentration of the analyzed solution was 0.0972%, the relative analysis error was 2.8%,
Результаты анализа растворов полиакрил амида и полиакрилонитрила, приготовленных на пластовой воде месторождени , содержащей сульфаты, нитраты, карбонаты в значительных количествах, приведены в таблице.The results of the analysis of solutions of polyacryl amide and polyacrylonitrile prepared on the reservoir water of the field containing sulphates, nitrates, and carbonates in significant quantities are listed in the table.
Точность определени известным способом равна 10%, Продолжительность анализа рабочей пробы предлагаемым способом 1 мин, а известным 1-1,5 ч,The accuracy of determination in a known manner is 10%. The duration of the analysis of a working sample by the proposed method is 1 min, and the known 1-1.5 h,
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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SU864143688A SU1451590A1 (en) | 1986-11-05 | 1986-11-05 | Method of quantitative analysis of polyacrylamide and polyacrylonitril in aqueous solutions |
Applications Claiming Priority (1)
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SU864143688A SU1451590A1 (en) | 1986-11-05 | 1986-11-05 | Method of quantitative analysis of polyacrylamide and polyacrylonitril in aqueous solutions |
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SU1451590A1 true SU1451590A1 (en) | 1989-01-15 |
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SU864143688A SU1451590A1 (en) | 1986-11-05 | 1986-11-05 | Method of quantitative analysis of polyacrylamide and polyacrylonitril in aqueous solutions |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108152286A (en) * | 2018-02-11 | 2018-06-12 | 广东出入境检验检疫局检验检疫技术中心 | A kind of kit and its detection method of quick qualification determination nitrite in cubilose content |
-
1986
- 1986-11-05 SU SU864143688A patent/SU1451590A1/en active
Non-Patent Citations (1)
Title |
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Авторское свидетельство СССР 773046, кл. С 08 F 20/56, 1978. * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108152286A (en) * | 2018-02-11 | 2018-06-12 | 广东出入境检验检疫局检验检疫技术中心 | A kind of kit and its detection method of quick qualification determination nitrite in cubilose content |
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