RU2010770C1 - Method of extraction of manganese, iron, zinc, copper, and lead out of natural and sewage waters - Google Patents
Method of extraction of manganese, iron, zinc, copper, and lead out of natural and sewage waters Download PDFInfo
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- RU2010770C1 RU2010770C1 SU4841391A RU2010770C1 RU 2010770 C1 RU2010770 C1 RU 2010770C1 SU 4841391 A SU4841391 A SU 4841391A RU 2010770 C1 RU2010770 C1 RU 2010770C1
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- natural
- zinc
- iron
- copper
- manganese
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 239000010949 copper Substances 0.000 title claims abstract description 12
- 229910052742 iron Inorganic materials 0.000 title claims abstract description 12
- 239000011701 zinc Substances 0.000 title claims abstract description 12
- 229910052725 zinc Inorganic materials 0.000 title claims abstract description 12
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims abstract description 5
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 title claims abstract description 4
- 239000010865 sewage Substances 0.000 title claims abstract 3
- 239000003643 water by type Substances 0.000 title claims abstract 3
- 239000011133 lead Substances 0.000 title abstract description 11
- 238000000605 extraction Methods 0.000 title abstract description 6
- 239000002594 sorbent Substances 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims description 8
- 229960004889 salicylic acid Drugs 0.000 claims description 3
- 238000011084 recovery Methods 0.000 claims description 2
- 239000013522 chelant Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 abstract description 3
- 239000002253 acid Substances 0.000 abstract description 3
- 229920002223 polystyrene Polymers 0.000 abstract description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 150000002739 metals Chemical class 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 1
- 229910052748 manganese Inorganic materials 0.000 description 7
- 239000011572 manganese Substances 0.000 description 7
- 238000001179 sorption measurement Methods 0.000 description 7
- 229910052745 lead Inorganic materials 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002351 wastewater Substances 0.000 description 3
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
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- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
Description
Изобретение относится к способам группового извлечения элементов (Mn, Fe, Zn, Cu, Pb) из природных и сточных вод для последующего их аналитического определения. The invention relates to methods for group extraction of elements (Mn, Fe, Zn, Cu, Pb) from natural and waste waters for their subsequent analytical determination.
Целью является увеличение избирательности и степени извлечения. Поставленная цель достигается способом извлечения предложенных микроэлементов из растворов путем введения полимерного хелатного сорбента полистирол - азо- салициловой кислоты, сорбцию проводят при рН 5,3-6,0 и при температуре 15-30оС.The goal is to increase selectivity and recovery. This goal is achieved by the method of extraction of the proposed trace elements from solutions by introducing a polymeric chelating sorbent polystyrene - azosalicylic acid, sorption is carried out at pH 5.3-6.0 and at a temperature of 15-30 about C.
Хелатный сорбент полистирол - азо-салициловая кислота HN= N представляет собой тонкодисперсный порошок темно-коричневого цвета, нерастворимый в воде, кислотах, щелочах и органических растворителях.Chelated sorbent polystyrene - azo-salicylic acid H N = n It is a fine powder of dark brown color, insoluble in water, acids, alkalis and organic solvents.
Сорбционная емкость сорбента по извлекаемым металлам составляет 21,7 мг ΣMn, Fe, Zn. Cu. Pb/Г сорбента. The sorption capacity of the sorbent for recoverable metals is 21.7 mg ΣMn, Fe, Zn. Cu. Pb / g sorbent.
Зависимость степени сорбции от рН среды представлена в табл. 1. Количественная сорбция (R= 95-100% ) наблюдается в следующих значений рН: для марганца 5,3-10,0; для цинка 5,0-8,0; для железа 3,7-10,0; меди 4,5-7,5; свинца 4,7-6,0. The dependence of the degree of sorption on the pH of the medium is presented in table. 1. Quantitative sorption (R = 95-100%) is observed in the following pH values: for manganese 5.3-10.0; for zinc, 5.0-8.0; for iron, 3.7-10.0; copper 4.5-7.5; lead 4.7-6.0.
Совместное количественное извлечение Mn, Fe, Zn, Cu, Pb происходит в интервале значений рН 5,3-6,0. Joint quantitative extraction of Mn, Fe, Zn, Cu, Pb occurs in the range of pH 5.3-6.0.
В табл. 2 представлены сравнительные результаты по избирательности групповой сорбции Mn, Fe, Zn, Cu, Pb предлагаемым сорбентом и известным наиболее широко используемым полистирол-азо-4-окси-3-арсонобензолом. Из таблицы следует, что избирательность групповой сорбции указанных элементов предлагаемым сорбентом выше избирательности на несколько порядков, чем известные сорбенты. Предлагаемый способ позволяет количественно извлекать Mn, Fe, Zn, Cu, Pb из природных и сточных вод в присутствии n˙102-n˙106 - кратных избыточных количеств Ca, Mg, K, Na, Ba, Sr, Li, AI, Ti.In the table. 2 presents comparative results on the selectivity of group sorption of Mn, Fe, Zn, Cu, Pb by the proposed sorbent and the most widely known polystyrene-azo-4-hydroxy-3-arsenobenzene. From the table it follows that the selectivity of the group sorption of these elements by the proposed sorbent is higher by several orders of magnitude than the known sorbents. The proposed method allows to quantitatively extract Mn, Fe, Zn, Cu, Pb from natural and wastewater in the presence of n 210 2 -n 610 6 - multiple excess amounts of Ca, Mg, K, Na, Ba, Sr, Li, AI, Ti.
В табл. 3 представлены данные по результатам сорбции от продолжительности перемешивания, а в табл. 4 - от температуры процесса. In the table. 3 presents data on the results of sorption on the duration of mixing, and in table. 4 - from the process temperature.
Сущность способа заключается в том, что в анализируемую воду, после создания соответствующей среды с рН 5,3-6,0, добавляют 50 мг сорбента, смесь перемешивают не менее 60 мин при температуре 15-30оС и фильтруют раствор через фильтр "белая лента", концентрат промывают водой и десорбируют элементы 1М HCl. В элюатах определение элементов выполняют методом атомно-абсорбционной спектроскопии или любым другим методом.The method consists in that the water to be analyzed after the creation of the appropriate medium at
Пример. Определение марганца, железа, цинка, меди и свинца в природных и сточных водах. Example. Determination of manganese, iron, zinc, copper and lead in natural and waste waters.
К 500 мл анализируемой воды, доведенной 2 М HCl до рН 5,3-6,0 прибавляют 50 мг сорбента полистирол-азо-салициловую кислоту. Раствору перемешивают на магнитной мешалке в течение не менее 60 мин при температуре 15-30оС. Сорбент отфильтровывают через фильтр "белая лента". Концентрат промывают 3-4 раза дистиллированной водой и десорбируют Mn, Fe, Zn, Cu, Pb 1M HCl. Элюат собирают в мерную пробирку емкостью 10 мл. В полученном растворе элементы определяют методом атомно-абсорбционной спектроскопии, работу выполняли с трехщелевой горелкой в пламени ацетилен-воздух. Источниками резонансного излучения были лампы полого катода.To 500 ml of analyzed water, adjusted with 2 M HCl to pH 5.3-6.0, 50 mg of the sorbent polystyrene-azo-salicylic acid are added. The solution was stirred on a magnetic stirrer for at least 60 minutes at a temperature of 15-30 ° C is filtered through a sorbent filter "white ribbon". The concentrate is washed 3-4 times with distilled water and stripped with Mn, Fe, Zn, Cu, Pb 1M HCl. The eluate is collected in a 10 ml volumetric tube. In the resulting solution, the elements are determined by atomic absorption spectroscopy; work was carried out with a three-gap burner in an acetylene-air flame. Sources of resonant radiation were hollow cathode tubes.
В табл. 5 представлены результаты определения Mn, Fe, Zn, Cu, Pb в стандартных образцах, аттестованных на содержание этих элементов. (56) Авторское свидетельство СССР N 1678872, кл. С 22 В 23/00, 1989. In the table. 5 presents the results of the determination of Mn, Fe, Zn, Cu, Pb in standard samples certified for the content of these elements. (56) Copyright certificate of the USSR N 1678872, cl. C 22 V 23/00, 1989.
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU4841391 RU2010770C1 (en) | 1990-06-21 | 1990-06-21 | Method of extraction of manganese, iron, zinc, copper, and lead out of natural and sewage waters |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU4841391 RU2010770C1 (en) | 1990-06-21 | 1990-06-21 | Method of extraction of manganese, iron, zinc, copper, and lead out of natural and sewage waters |
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|---|---|
| RU2010770C1 true RU2010770C1 (en) | 1994-04-15 |
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| SU4841391 RU2010770C1 (en) | 1990-06-21 | 1990-06-21 | Method of extraction of manganese, iron, zinc, copper, and lead out of natural and sewage waters |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2262102C1 (en) * | 2004-02-11 | 2005-10-10 | Государственное образовательное учреждение высшего профессионального образования "Красноярский государственный университет" | Indicator composition for determining manganese(ii) in aqueous solutions |
| RU2394775C1 (en) * | 2008-12-09 | 2010-07-20 | Лидия Алексеевна Воропанова | Method of extracting lead ions from aqueous solution |
| CN102600980A (en) * | 2012-03-19 | 2012-07-25 | 赤峰中色锌业有限公司 | Recycling method for mineral processing waste water with high leaching residue content in zinc hydrometallurgy |
-
1990
- 1990-06-21 RU SU4841391 patent/RU2010770C1/en active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2262102C1 (en) * | 2004-02-11 | 2005-10-10 | Государственное образовательное учреждение высшего профессионального образования "Красноярский государственный университет" | Indicator composition for determining manganese(ii) in aqueous solutions |
| RU2394775C1 (en) * | 2008-12-09 | 2010-07-20 | Лидия Алексеевна Воропанова | Method of extracting lead ions from aqueous solution |
| CN102600980A (en) * | 2012-03-19 | 2012-07-25 | 赤峰中色锌业有限公司 | Recycling method for mineral processing waste water with high leaching residue content in zinc hydrometallurgy |
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