期刊文献+

苯酚表面分子印迹聚合物的吸附性能研究

Study on Adsorption Properties of Phenol Surface Molecularly Imprinted Polymers
在线阅读 下载PDF
导出
摘要 为高效分离、富集和回收废水中的苯酚提供一种新的吸附材料。以改性纳米二氧化硅为载体,采用表面分子印迹技术制备苯酚表面分子印迹聚合物(SiO_(2)^(-)SMIP)和空白表面分子印迹聚合物(SiO_(2)^(-)SNIP);动态吸附、静态吸附、选择性吸附、再生吸附和竞争吸附实验用以探究其吸附性能。SiO_(2)^(-)SMIP对苯酚具有良好的吸附能力,吸附过程属于单吸附层的化学吸附,可快速达到吸附平衡;SiO_(2)^(-)SMIP比SiO_(2)^(-)SNIP具有更多的亲和力结合位点和更高的最大表观结合量,且对苯酚具有特异的选择性吸附能力;SiO_(2)^(-)SMIP经过多次循环使用后,对苯酚依然具有很好的吸附能力。SiO_(2)^(-)SMIP吸附能力出色、性质稳定、特异选择性高,可作为吸附剂材料有效分离、富集和回收废水中的苯酚。 A new adsorption material for the efficient separation,enrichment,and recovery of phenol in wastewater was provided.Phenol surface molecularly imprinted polymers(SiO_(2)^(-)SMIP)and blank surface molecularly imprinted polymers(SiO_(2)^(-)SNIP)were prepared by a surface molecular imprinting technique using modified nanosilicon dioxide as the carrier.Dynamic adsorption,static adsorption,selective adsorption,regeneration adsorption,and competitive adsorption experiments were carried out to investigate the adsorption properties of SiO_(2)^(-)SMIP and SiO_(2)^(-)SNIP.The results showed that the SiO_(2)^(-)SMIP has a good adsorption capacity for phenol.The adsorption process belongs to the chemisorption of a single adsorption layer,and the adsorption equilibrium can be reached quickly.SiO_(2)^(-)SMIP has more affinity binding sites and a higher maximum apparent binding capacity than SiO_(2)^(-)SNIP,and has a specific selective adsorption capacity for phenol.After repeated use,SiO_(2)^(-)SMIP still has a good adsorption capacity for phenol.SiO_(2)^(-)SMIP has excellent adsorption capacity,stable properties,and high specific selectivity.It can be used as an adsorbent material to effectively separate,enrich,and recover phenol from wastewater.
作者 常自强 邓波 饶安举 CHANG Zi-qiang;DENG Bo;RAO An-ju(School of Public health,North Sichuan Medical College,Nanchong 637000,China)
出处 《化学试剂》 2025年第2期39-45,共7页 Chemical Reagents
关键词 苯酚 分子印迹聚合物 选择性 吸附性能 废水处理 phenol molecularly imprinted polymers selectivity adsorption property wastewater treatment
  • 相关文献

参考文献10

二级参考文献75

共引文献30

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