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Modification of activated carbon with a silane coupling agent under ultrasonic conditions for the advanced treatment of wastewater with dressing chemicals

机译:在超声条件下用硅烷偶联剂对活性炭进行改性,以利用选矿化学品对废水进行深度处理

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摘要

Fresh activated carbon (FAC) was oxidised by nitric acid and then the silane coupling agent was grafted onto the surface of FAC under ultrasonic conditions to obtain modified activated carbon (MAC). The chemical oxygen demand was used as the main evaluation index in the wastewater. The effects of benzene, aniline, 2-mercaptobenzothiazole and methylene blue on the adsorption mechanism and performance of FAC prior and postmodification were investigated by different adsorption models. All of them fitted the Langmuir monomolecular adsorption model. The adsorption capacity of MAC was 1.07, 1.12, 1.56 and 0.62 times that of FAC, respectively, which had a better adsorption effect on hydrophobic organic compounds. The maximum adsorption capacity increased due to the existence of competitive adsorption in multicomponent absorption. Texture properties of activated carbon were characterised by scanning electron microscopy, Fourier Transform-infrared and Brunauer-Emmett-Teller theory, which show that the surface morphology became spongy, and that Si-O-C and Si-O infrared peaks appeared. In addition to the mesopore volume, the specific surface area, pore volume and micropore volume decreased slightly after the modification.
机译:将新鲜的活性炭(FAC)用硝酸氧化,然后在超声条件下将硅烷偶联剂接枝到FAC的表面上,以获得改性的活性炭(MAC)。化学需氧量被用作废水中的主要评价指标。通过不同的吸附模型研究了苯,苯胺,2-巯基苯并噻唑和亚甲基蓝对FAC吸附前后机理的影响。它们都符合Langmuir单分子吸附模型。 MAC的吸附量分别是FAC的1.07、1.12、1.56和0.62倍,对疏水性有机化合物的吸附效果更好。由于多组分吸收中竞争性吸附的存在,最大吸附容量增加。活性炭的织构特性通过扫描电子显微镜,傅里叶变换红外光谱法和Brunauer-Emmett-Teller理论表征,表明其表面形态呈海绵状,并出现Si-O-C和Si-O红外峰。除中孔体积外,比表面积,孔体积和微孔体积在改性后略有下降。

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  • 来源
    《Coloration Technology 》 |2019年第1期| 67-76| 共10页
  • 作者单位

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China|Cent S Univ, Natl Engn Lab Efficient Utilizat Refractory Nonfe, Changsha 410083, Peoples R China;

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China;

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China;

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China;

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China;

    Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China;

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