49 research outputs found

    ВЛИЯНИЕ ПОВЕРХНОСТНОГО МОДИФИЦИРОВАНИЯ ГИДРАТИРОВАННОГО ДИОКСИДА ТИТАНА НА СЕЛЕКТИВНОСТЬ ПО ОТНОШЕНИЮ К СТРОНЦИЮ

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    The effect exerted on the selectivity of hydrated TiO2 to Sr by surface modification of the sorbent involving immobilization of mixed nickel potassium ferrocyanide was studied. The Sr specificity of the resulting sorbent (denoted as T-55) is comparable with that of hydrated TiO2: logK d (K d is Sr distribution coefficient, ml g-1) is 2.7 ± 0.2 in sorption from tap water with pH 7.8 ± 0.2, 2.7 ± 0.5 in sorption from CaCl2 solutions with pH 5.6 ± 0.2, and from 2.5 ± 0.8 to 1.7 ± 0.4 in sorption from CaCl 2 solutions with pH 7.0 ± 0.2. The modification makes the resulting T-55 sorbent selective to Sr in the presence of Ca at pH 5-6. © 2013 Pleiades Publishing, Ltd

    ВЛИЯНИЕ КОНЦЕНТРАЦИИ КАЛИЯ, НАТРИЯ И АММОНИЯ НА СОРБЦИЮ ЦЕЗИЯ СМЕШАННЫМ ФЕРРОЦИАНИДОМ НИКЕЛЯ-КАЛИЯ НА ОСНОВЕ ГИДРАТИРОВАННОГО ДИОКСИДА ТИТАНА

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    The effect of single-charged cations (Na+, K+, NH 4 +) on the cesium sorption with mixed nickel potassium ferrocyanide sorbent based on hydrated TiO2 was studied. The K + and Na+ ions exert no effect at their concentrations of up to 0.5 M; the Cs+ distribution coefficients from KCl and NaCl solutions are (1.1 ± 0.5) Ч 105 and (8 ± 3) Ч 104 mL g-1, respectively. The sorbent is highly specific to Cs+ in the presence of ammonium ions. The sorption mechanisms were studied. The concentration ranges in which Cs+ and NH 4 + are sorbed by independent mechanisms (Cs+, by the ferrocyanide phase; NH 4 +, by the phase of hydrated TiO2) and in which the Cs+ distribution coefficient decreases owing to competitive filling of the ferrocyanide phase with ammonium ions were determined. At cesium concentrations in solution exceeding 50 mg L-1, Cs+ and NH 4 + are absorbed jointly owing to coprecipitation in the mixed ferrocyanide phase in the pore space of the sorbent. © 2013 Pleiades Publishing, Ltd

    Peculiarities of sorption isotherm and sorption chemisms of caesium by mixed nickel-potassium ferrocyanide based on hydrated titanium dioxide

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    Sorption isotherm of caesium from tap water by mixed nickel-potassium ferrocyanide based on hydrated titanium dioxide is obtained for a wide range of concentrations of caesium. It is shown that there are three types of specificity to caesium sorption sites in this sorbent. Sorption chemisms of caesium are studied, factors conditioned high sorption capacity of the sorbent are revealed. It is shown that occupation of sorption sites I and II is well approximated by Langmuir equilibrium and this process can be described within the bounds of theory of ion exchange. The expected sorption chemism of caesium by sorption sites III at high concentrations of caesium (>50 mg L-1) is precipitation of mixed nickel-caesium ferrocyanide in pore space of the sorbent. © 2013 Akadémiai Kiadó, Budapest, Hungary

    Изучение закономерностей синтеза тонкослойных неорганических сорбентов и областей их применения для извлечения радионуклидов из жидких радиоактивных отходов

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    Объектами исследования являются поверхностно-модифицированные ферроцианидные сорбенты на основе гидратированного диоксида титана. Целью данной работы является изучение закономерностей синтеза поверхностно-модифицированных неорганических сорбентов и способов их применения для переработки жидких радиоактивных отходов и иммобилизации радионуклидов цезия и стронция. В ходе работы был поставлен ряд экспериментов по изучению закономерностей синтеза смешанного ферроцианида никеля-калия на основе гидратированного диоксида титана (сорбент Т-55), исследованы механизмы и закономерности сорбции радионуклидов синтезированным сорбентом в присутствии различных мешающих примесей, возможности иммобилизациии радионуклидов цезия и стронция. На основании полученных экспериментальных данных были сделаны выводы о возможных сферах применения синтезированного сорбента для переработки ЖРО различного состава и для сорбционного концентрирования в методах анализа природных вод и технологических растворов на радионуклиды цезия. По результатам, полученным в данной работе, написано 2 статьи в зарубежные рецензируемые журналы и 4 тезиса докладов на конференции.Программа развития УрФУ на 2013 год (п.2.1.1.1

    A technology of drinking water decontamination from radon and its decay products

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    Underground water is one of the main sources of radon for households. This article focuses on the estimation and removal of radon from underground water using the technology and inorganic sorbents developed by EKSORB Ltd., Russia for liquid radioactive waste treatment in the nuclear power industry. The article presents the results of tests of a system for the removal of radon and radon daughters from water patented by EKSORB. This is achieved by filtering water through RATZIR sorbent, followed by periodic load regeneration. Over a period of three years, the plant is successful in removing radon from the water that had an initial radon content of approximately 1500 Bq/L to less than 60 Bq/L, without releasing radon to indoor/outdoor air. © 2020 Igor Voinov et al., published by Sciendo 2020

    Статика и кинетика сорбции цезия из водных сред ферроцианидами никеля-калия на основе гидратированных диоксидов титана и циркония

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    Optimization of the synthesis of the mixed nickel-potassium ferrocyanide based on hydrated titanium dioxide has been realized. The influence of the conditions of synthesis of the sorbents on the elemental composition, surface texture, statics and kinetics has been shown. The synthetic technique was used to prepare sorbents based on hydrated titanium dioxide carrier. The influence of the chemical properties of the carrier on sorption behaviour of the ferrocyanides was determined.Описана оптимизация синтеза смешанного ферроцианида никеля-калия на основе гидратированного диоксида титана. Показано влияние условий синтеза сорбентов на их элементный состав, текстуру поверхности, статику и кинетику сорбции. Методика синтеза была использована для получения сорбента на основе гидратированного диоксида титана. Определено влияние химических свойств носителя на сорбционное поведение ферроцианидов

    Impact of Pollutants of Natural and Anthropogenic Origin on the Quality of Wastewater in Ekaterinburg

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    The object of the study was river water, which was sampled 500 m before and 500 m after the point of discharge of wastewaters from industrial activities. The concentration of chlorides, magnesium, and calcium in all the studied samples was below the value of the acceptable limit concentration. The pH of the water samples and the sulphate concentration were within acceptable limits. The concentration of iron, ammonium, and nitrite in water samples was higher than the value of acceptable limit. It was suggested that water pollution with iron and nitrite was mainly due to natural processes, and the presence of ammonium and oil products could be explained by anthropogenic sources. © Published under licence by IOP Publishing Ltd.The article was prepared with the financial support of Competitiveness Enhancement Program – CEP 3.1.1.1-20

    STUDY OF RADIUM-223 SORPTION BY THIN-LAYER SORBENTS BASED ON MANGANESE DIOXIDE ON VARIOUS POLYMER SUPPORTS

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    The work is devoted to the study of radium-223 sorption by thin-layer sorbents based on manganese dioxide on various polymer supports. The effect of salt content and solid/liquid ratio was evaluated. Comparison of sorption properties of various polymer supports was per-formed.Исследование выполнено при финансовой поддержке РФФИ в рамках научного проекта № 20-03-00931

    Development and Approbation of a Method for Analysis of the Uranium Isotopic Ratio of in Technological Solutions at Uranium Mining Enterprises

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    The article describes the development and approbation of a method for analysis of the isotopic composition of uranium in technological solutions of the uranium mining enterprise and identifies the optimal parameters for each stage of analysis in order to achieve the maximum degree of uranium recovery from productive solutions (PR).В статье описывается разработка и апробация метода анализа изотопного состава урана в технологических растворах урандобывающего предприятия и определяются оптимальные параметры для каждой стадии анализа с целью достижения максимальной степени извлечения урана из продуктивных растворов (ПР)
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