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作 者:Wittaya Chuajiw Mitsuru Nakano Kazumasa Takatori Toshiya Kojima Yoshiki Wakimoto Yoshiaki Fukushima
机构地区:[1]Toyota Technological Institute,2-12-1 Hisakata,Tempaku-ku,Tenpaku Moon Chome [2]Toyota Central R&D Labs. Inc.,Yokomichi [3]Aisin Seiki Co.,Ltd.,2-1,Asahi-machi
出 处:《Journal of Environmental Sciences》2013年第12期2507-2515,共9页环境科学学报(英文版)
摘 要:The amount of carbon dioxide (CO2) absorption and calcium ion (Ca^2+) concentration besides the pH of aqueous solution were observed during the COz absorption to precipitate calcium carbonate (CaCO3) from calcium hydroxide (Ca(OH)2). A reaction rate-limiting effect of an amount of CO2 absorption without any organic additives in the early stage of the precipitation was observed, which was attributed to an interruption effect of bicarbonate ion (HCO3) on the precipitation of CaCO3. The improvement for the reaction rate was achieved not only by amine additives but also by neutral additives such as ε-caprolactam or amine salt. When the hexamethylene diamine was dissolved in the solution, successive change of crystal forms of CaCO3 aragonite to calcite in aqueous suspensions, confirmed by Ca^2+ concentration change and X-ray diffraction, was concluded that a local environment around the amine group in aqueous solution and an interaction of the diamine with precipitated CaCO3 particles were important factors for these reactions.The amount of carbon dioxide (CO2) absorption and calcium ion (Ca^2+) concentration besides the pH of aqueous solution were observed during the COz absorption to precipitate calcium carbonate (CaCO3) from calcium hydroxide (Ca(OH)2). A reaction rate-limiting effect of an amount of CO2 absorption without any organic additives in the early stage of the precipitation was observed, which was attributed to an interruption effect of bicarbonate ion (HCO3) on the precipitation of CaCO3. The improvement for the reaction rate was achieved not only by amine additives but also by neutral additives such as ε-caprolactam or amine salt. When the hexamethylene diamine was dissolved in the solution, successive change of crystal forms of CaCO3 aragonite to calcite in aqueous suspensions, confirmed by Ca^2+ concentration change and X-ray diffraction, was concluded that a local environment around the amine group in aqueous solution and an interaction of the diamine with precipitated CaCO3 particles were important factors for these reactions.
关 键 词:carbon dioxide absorption calcium carbonate precipitation local functional group interaction
分 类 号:X13[环境科学与工程—环境科学]
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