期刊文献+

有机粘土疏水性吸附过程的分子模拟:烷基碳原子数和有机物logK_(ow)的影响 被引量:2

Molecular simulation of the hydrophobic adsorption of organoclay:Effects of the alkyl chain length and the hydrophobicity of organic compounds
原文传递
导出
摘要 基于从分子尺度上解析改性剂烷基碳原子数和有机物疏水性对有机粘土吸附能力的影响机制,以从头算的量子化学计算方法(MP2/6-31g(d))模拟了有机粘土在水溶液中的吸附过程.通过计算吸附前后几何构型、能量、化学键和电荷分布等参数的变化,分析了影响有机粘土疏水性吸附的关键因素,并对疏水性吸附作用力的化学本质进行了初步探讨.计算结果表明,烷基碳原子数增加对提高有机物吸附能的作用并不显著,长链烷基提高有机粘土吸附容量的真正原因在于其可提供更多的有机物吸附位.有机物的疏水性(以正辛醇-水分配系数logKow表征)是影响疏水性吸附过程的关键因子,水分子的引力作用对疏水性吸附具有决定性影响,理论上解释了普遍存在的有机物吸附量与logKow呈正相关的实验现象.疏水性吸附力的作用前提是有机物为疏水性,即当水分子的引力作用较弱时疏水性作用力才可以表现出来;而对于亲水性有机物,疏水性吸附力会被水分子的引力所抵消,吸附强度减弱.模拟红外光谱和电荷分布结果表明,吸附前后无化学键断裂和电子得失的发生,只有原子电荷密度的微小变化,据此推测疏水性吸附力以分子间弱相互作用力——London色散力为主. Based on the effects of the alkyl chain length of modifier and the hydrophobicity of organic compounds,the adsorption behavior and capability of organoclay in aqueous system were simulated by the quantum chemical calculation(ab initio MP2/6-31g(d)).By calculating the changes of geometric configuration,energy,chemical bond and charge distribution before and after the adsorption,the key factors and the chemical nature of hydrophobic force were investigated and discussed.The calculation results showed that the increase of the alkyl chain length(from 2 to 6) had an insignificant effect on the adsorption energy.The reason responsible for improvement of adsorption capacity was that long chain-alkyl can provide more sites for organic molecules.The hydrophobicity of the organic compounds,characterized as octanol-water partition coefficient(logKow),was the crucial factor for the hydrophobic adsorption and the attraction strength by water molecules played a critical role in the adsorption.Based on these results,it can be theoretically explained that the uptake of organic compounds had a good linear correlation with their logKow.The simulation results of the infrared spectroscopy and the atom charge distribution indicated that the fracture of chemical bond and the electron transfer did not occur,and that there was only small change of atom charge distribution.It was inferred that London dispersion force,which is a kind of van der waals force,contributed to the hydrophobic force.
出处 《环境科学学报》 CAS CSCD 北大核心 2012年第9期2049-2057,共9页 Acta Scientiae Circumstantiae
基金 国家自然科学基金重点项目(No.21037001) "十一五"国家科技支撑计划(No.2008BAC32B06-1)~~
关键词 有机粘土 疏水性吸附 分子模拟 MP2 London色散力 organoclay hydrophobic adsorption molecular simulation MP2 London dispersion force
  • 相关文献

参考文献35

  • 1Azejjel H, del Hoyo C, Draoui K, et al. 2009. Natural and modified Clays from Morocco as sorbents of ionizable herbicides in aqueous medium [J]. Desalination, 249(3): 1151-1158.
  • 2Bartelt-Hunt S L, Burns S E,Smith J A. 2003. Nonionic organic solute sorption onto two organobentonites as a function of organic-carbon content [ J]. Journal of Colloid and Interface Science, 266 (2) : 251-258.
  • 3Bernardoni F, Fadeev A Y. 2011. Adsorption and wetting characterization of hydrophobic SBA- 15 silicas [ J 1. Journal of Colloid and Interface Science, 356 (2) : 690-698.
  • 4Bucheli T D, Gustafsson O. 2000. Quantification of the soot-water distribution coefficient of PAHs provides mechanistic basis for enhanced sorption observations [ J ]. Environmental Science & Technology, 34(24) : 5144-5151.
  • 5Bundschuh M, Schulz R. 2011. Ozonation of secondary treated wastewater reduces ecotoxicity to Gammarus fossarum (Crustacea; Amphipoda) : Are loads of (micro)pollutants responsible? [ J]. Water Research, 45 ( 13 ) : 3999-4007.
  • 6Changchaivong S, Khaodhiar S. 2009. Adsorption of naphthalene and phenanthrene on dodecylpyridinium-modified bentonite [J]. Applied Clay Science, 43(3/4) : 317-321.
  • 7Cygan R T, Guggenheim S, Koster van Groos A F. 2004. Molecular models for the intercalation of methane hydrate complexes in montmorillonite clay [ J]. The Journal of Physical Chemistry B, 108 (39) : 15141-15149.
  • 8Efremenko I, Sheintuch M. 2006. Predicting solute adsorption on activated carbon: Phenol [J]. Langmuir, 22(8) : 3614-3621.
  • 9Fuller M, Smith J A, Burns S E. 2007. Sorption of nonionic organic solutes from water to tetraalkylammonium bentonites: Mechanistic considerations and application of the Polanyi-Manes potential theory [J]. Journal of Colloid and Interface Science, 313(2) : 405-413.
  • 10高海鹰,赵苏,李贺.阴-阳离子协同改性凹土对三氯乙烯的吸附[J].环境科学与技术,2011,34(S1):31-34. 被引量:4

二级参考文献41

共引文献189

同被引文献39

  • 1任源,韦朝海,吴超飞,吴锦华,谭展机.生物流化床A/O^2工艺处理焦化废水过程中有机组分的GC/MS分析[J].环境科学学报,2006,26(11):1785-1791. 被引量:88
  • 2Ozcan A S, Erdem B, Ozcan A. Adsorption of Acid Blue 193 from aqueous solutions onto Na-bentonite and DTMA-bentonite [ J]. Journal of Colloid and Interface Science, 2004, 280 ( 1 ) : 44-54.
  • 3Yapar S, Ozbudak V, Dias A, et al. Effect of adsorbent concentration to the adsorption of phenol on hexadecyl trimethyl ammonium-bentonite[ J]. Journal of Hazardous Materials, 2005, 121(1-3) : 135-139.
  • 4Rytwo G, Kohavi Y, Botnick I, et al. Use of CV- and TPP- montmorillonite for the removal of priority pollutants from water [J]. Applied Clay Science, 2007, 36(1-3): 182-190.
  • 5Bouberka Z, Khenifi A, Mahamed H A, et al. Adsorption of Supranol Yellow 4 GL from aqueous solution by surfactant-treated aluminum/chromium-intercalated bentonite [ J ]. Journal of Hazardous Materials, 2009, 162( 1 ) : 378-385.
  • 6Zhu R L, Wang T, Ge F, et al. Intercalation of both CTMAB and All3 into montmorillonite [ J ]. Journal of Colloid and Interface Science, 2009, 335( 1 ) : 77-83.
  • 7Zohra B, Aicha K, Fatima S, et al. Adsorption of Direct Red 2 on bentonite modified by cetyhrimethylammonium bromide [ J ]. Chemical Engineering Journal, 2008, 136 (2-3) : 295-305.
  • 8Yan L G, Wang J, Yu H Q, et al. Adsorption of benzoic acid by CTAB exchanged montmorillonite [ J]. Applied Clay Science,2007, 37(3-4): 226-230.
  • 9Da Silva U G Jr, De F Melo M A, Da Silva A F, et al. Adsorption of crude oil on anhydrous and hydrophobized vermiculite[J]. Journal of Colloid and Interface Science, 2003, 260(2) : 302-304.
  • 10Williams-Daryn S, Thomas R K. The intercalation of a vermiculite by cationic surfactants and its subsequent swelling with organic solvents [ J ]. Journal of Colloid and Interface Science, 2002, 255 ( 2 ) : 303- 311.

引证文献2

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部