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51.
Traditional preparation of superhydrophobic absorbents relies on solvents or further modification with silane. For environmental reasons, it is ideal to find ways that reduce or completely non-solvent. Herein, we show that superhydrophobic sponges can be obtained without solvents by the foaming process. Rough surface morphology and low surface energy were achieved simultaneously during the formation of superhydrophobic foam without further modification. The time required for oil–water separation was shortened significantly, when combined the sponge with a vacuum system. Importantly, the obtained sponge can retain its high oil absorption capacity after several cycles of oil–water separation. The sponge is easy to be scaled up and we have fabricated foams in large scale (37 cm × 30 cm × 22 cm) for making it an ideal candidate for practical application. 相似文献
52.
Fomkin A. A. Dubovik B. A. Limonov N. V. Pribylov A. A. Pulin A. L. Men’shchikov I. E. Shkolin A. V. 《Protection of Metals and Physical Chemistry of Surfaces》2021,57(1):17-21
Protection of Metals and Physical Chemistry of Surfaces - An EC-103 microporous carbon adsorbent was synthesized from wood using thermochemically activation with Н3РО4 as an... 相似文献
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I. E. Men’shchikov A. A. Fomkin A. B. Arabei A. V. Shkolin E. M. Strizhenov 《Protection of Metals and Physical Chemistry of Surfaces》2016,52(4):575-580
Temperature dependences of parameters n and E are calculated according to the adsorption equation of Dubinin–Astakhov for methane adsorption on eight active carbons in the range of supercritical temperatures of 170–340 K and pressures of 0–20 MPa. At temperatures above ~240 K, characteristic adsorption energy E of methane grows linearly at an increase in temperature. The temperature coefficients of characteristic energy of methane adsorption on active carbon tend to decrease at an increase in standard characteristic adsorption energy E0. The average value of parameter <n> for the studied adsorbents tends to grow at an increase in standard characteristic adsorption energy E0. 相似文献
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Solovtsova O. V. Shkolin A. V. Men’shchikov I. E. Knyazeva M. K. Fomkin A. A. Tsivadze A. Yu. Aksyutin O. E. Ishkov A. G. Khozina E. V. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(6):1080-1084
Protection of Metals and Physical Chemistry of Surfaces - In the present work, a method for producing new shaped composite materials by introducing a metal-organic framework structure Cu-BTC110... 相似文献
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煤炭企业引入职业安全卫生管理体系,将使煤炭企业由被动管理向主动管理转变,经验管理向科学管理转变。本文结合煤炭企业的特点,提出了煤炭企业建立职业安全卫生管理体系的具体可行方法。 相似文献
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Danuta Kuzmicz Paul Coupillaud Yongjun Men Joan Vignolle Giordano Vendraminetto Martina Ambrogi Daniel Taton Jiayin Yuan 《Polymer》2014
Ionic liquid-functionalized mesoporous polymeric networks with specific surface area up to 935 m2/g have been successfully synthesized one pot by solvothermal copolymerization of divinylbenzene and monomeric ionic liquids. The as-obtained polymers exhibit a monolithic structure featuring large pore volumes, an abundant mesoporosity and an adjustable content of ionic liquids. The effect of the reaction conditions on the pore structure has been studied in detail. These poly(ionic liquid)-based porous networks (PILPNs) have then been employed as precursors in two distinct applications, namely organocatalysis and production of microporous carbon monoliths. Selected organocatalyzed reactions, including carbonatation of propylene oxide by cycloaddition with carbon dioxide, benzoin condensation, and cyanosilylation of benzaldehyde have been readily triggered by PILPNs acting as crosslinked polymer-supported (pre)catalysts. The two latter reactions required the prior deprotonation of the imidazolium salt units with a strong base to successfully generate polymer-supported N-heterocyclic carbenes, referred to as poly(NHC)s. Facile recycling and reuse of polymer-supported (pre)catalysts was achieved by simple filtration owing to the heterogeneous reaction conditions. Furthermore, PILPNs could be easily converted into microporous carbon monoliths via CO2 activation. 相似文献