期刊文献+

三嗪-三苯胺基磁性吸附剂Ni/CTP_(CC-TPA)用于水中硝基苯酚的吸附

Triazine-triphenylamine magnetic adsorbent Ni/CTP_(CC-TPA) for the adsorption of nitrophenol in water
下载PDF
导出
摘要 污水治理是当今社会面临的一大难题。通过傅-克反应以三聚氰氯和三苯胺为原料合成一种新型共价三嗪聚合物并加镍磁化用于污水中硝基苯酚的吸附。从化学结构上看,三嗪环和芳香环的存在提供疏水和π-π相互作用。测得三嗪-三苯胺材料S BET=680 m^(2)·g^(-1),孔径在2 nm左右,磁化后的比表面积仅为170 m^(2)·g^(-1),这与Ni占据了少量吸附位点有关。从热力学、动力学角度介绍了吸附过程和吸附机理,同时评价了不同pH和盐浓度对吸附的影响。吸附实验表明,对硝基苯酚和2,4-二硝基苯酚的吸附主要为物理吸附,而2,4,6-三硝基苯酚的吸附为化学吸附。 Nowadays,the sewage treatment is a major problem in society.A novel covalent triazine polymer was synthesized from cyanuric chloride and triphenylamine by Friedel-Crafts reaction and magnetized with nickel for the adsorption of nitrophenol in sewage.From the chemical structure,the presence of triazine and aromatic rings provides hydrophobic and π-π interactions.The Brunauer-Emmett-Teller(BET)surface area of triazine-trianiline material is 680 m^(2)·g^(-1) and the pore size is about 2 nm.The specific surface area after magnetization is only 170 m^(2)·g^(-1).The adsorption process and mechanism were introduced from thermodynamics and kinetics,and the effects of different pH values and salt concentrations on the adsorption were evaluated.Adsorption experiments show that the adsorptions of p-nitrophenol and 2,4-dinitrophenol belong to the physical adsorption,while the adsorption of 2,4,6-trinitrophenyl phenol belongs to chemical adsorption.
作者 王媛 甘修培 付蒙蒙 赵文杰 WANG Yuan;GAN Xiupei;FU Mengmeng;ZHAO Wenjie(College of Chemistry and Chemical Engineering,Henan University of Technology,Zhengzhou 450001,Henan,China)
出处 《化学研究》 CAS 2021年第2期152-159,共8页 Chemical Research
基金 国家自然科学基金资助项目(21675040) 河南省高校科技创新人才资助项目(20HASTIT007)。
关键词 共价三嗪聚合物 磁性吸附剂 硝基苯酚 covalent triazine polymer magnetic adsorbent nitrophenol
  • 相关文献

参考文献4

二级参考文献43

  • 1宁艳春,段巧丽,王兆花,陈绮莉.膜分离技术在废水处理方面的应用与进展[J].化工进展,2011,30(S1):828-830. 被引量:9
  • 2张德强,康海彦,杨莉丽,李娜,高丽荣.离子交换树脂吸附Cd(Ⅱ)和Pb(Ⅱ)的研究[J].环境科学与技术,2003,26(S1):4-5. 被引量:18
  • 3LI A, LU R F, WANG Y, et al. Lithium-doped conjugated microporous polymers for reversible hydro- gen storage [J]. Angew Chem Int Ed, 2010, 49:3330--3333.
  • 4GAO X, ZOU X, MA H, et al. Highly selective and permeable porous organic framework membrane for CO2 capture [J]. Adv Mater, 2014, 26: 3644--3648.
  • 5XU Y, CHEN L, GUO Z, et al. Light-emitting conjugated polymers with microporous network architecture: interweaving scaffold promotes e- lectronic conjugation, facilitates exciton migration, and improves luminescence [J]. J Am Chem Soe, 2011, 133: 17622--17625.
  • 6DEBLASE C R, SILBER- STEIN K E, TRUONG T T, et al. /?-Ketoenamine- linked covalent organic frameworks capable of pseudoca- pacitive energy storage [J]. J Am Chem Soc, 2013, 135: 16821--16824.
  • 7ZHAO M, OU S, WU C, et al. Porous metal-organic frameworks for heterogeneous biomimetic catalysis [J]. Ace Chem Res, 2014, 47: 1199--1207.
  • 8BEN T, REN H, MA S, et al. Targeted synthesis of a porous aromatic framework with high stability and exceptionally high surface area[J']. Angew Chem Int Ed, 2009, 48.. 9457- 9460.
  • 9XIE Z, WANG C, DEKRAFFT K E, et al. Highly stable and porous cross- linked polymers for efficient photocatalysis[J]. J Am Chem Soc, 2011, 133: 2056--2059.
  • 10CHENG G, HASELL T, TREWIN A, et al. Solu- ble conjugated microporous polymers [J]. Angew Chem Int Ed, 2012, 51: 12727--12731.

共引文献14

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