首页> 外文会议>International conference of the kolloid-gesellschaft >Adsorption from aqueous phenol and 2,3,4-trichlorophenol solutions on nanoporous carbon prepared from poly(ethylene terephthalate)
【24h】

Adsorption from aqueous phenol and 2,3,4-trichlorophenol solutions on nanoporous carbon prepared from poly(ethylene terephthalate)

机译:从聚(对苯二甲酸乙二醇酯)制备的纳米多孔碳水溶液和2,3,4-三氯苯酚溶液的吸附

获取原文

摘要

Highly microporous poly(ethylene terephthalate) based activated carbon exhibits a Bru-nauer-Emmett-Teller surface area of 1170 m~2/g and a total pore volume of 0.625 cm~3/g. It contains mesopores in a sufficient proportion of 42% of the total pore volume, which promotes the diffusion availability of the micropore region. The surface possesses an amphoteric nature owing to the oxygen functionalities present; however, the majority of the groups are basic. The adsorption properties from aqueous solution of weak acids, such as phenol and 2,3,4-trichlorophenol, depend both on the pH of the solutions and on the pK_a of the phenols, as the pH influences both the surface chemistry of the carbon and the dissociation of the weak acids used. In the case of phenol, a competitive adsorption takes place, as the interactions are weak in the three media investigated (pH 3, unbuffered and pH 11). The triple chlorine substitution in 2,3,4-trichlorophenol significantly enhances the surface interactions. Owing to the smaller pK_a value of trichloro-phenol in an unbuffered medium, ionic interaction occurs as has been concluded from the outstandingly high value of the adsorption equilibrium constant. At pH 11 the adsorption of the phenols is hindered by electrostatic repulsion.
机译:高度微孔聚(对苯二甲酸乙二酯)基活性炭展品1170米〜2 / g的BRU-nauer - 埃米特 - 特勒表面积和0.625厘米〜3 / g的总孔体积。它包含的总孔体积,这促进微孔区域的扩散可用性42%的足够比例中孔。表面具有由于氧官能团存在的两性性质;然而,大部分的基团是基本的。从弱酸,如苯酚和2,3,4-三氯苯酚水溶液的吸附性能,既取决于溶液的pH和对酚的pK_a,随着pH的影响两个碳的表面化学和的弱酸解离使用。在苯酚的情况下,有竞争力的吸附发生时,作为相互作用在所研究的三种介质(pH为3,非缓冲的和pH 11)弱。在2,3,4-三氯三氯取代显著增强了表面的相互作用。由于在无缓冲介质三氯苯酚的小pK_a值,离子相互作用发生如已经从吸附平衡常数的显着地高的值的结论。在pH11的酚的吸附是通过静电排斥阻碍。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号