首页> 美国卫生研究院文献>Nanoscale Research Letters >Nanostructure of Poly(Acrylic Acid) Adsorption Layer on the Surface of Activated Carbon Obtained from Residue After Supercritical Extraction of Hops
【2h】

Nanostructure of Poly(Acrylic Acid) Adsorption Layer on the Surface of Activated Carbon Obtained from Residue After Supercritical Extraction of Hops

机译:啤酒花超临界萃取后残留物中获得的活性炭表面上的聚丙烯酸吸附层的纳米结构

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The nanostructure of poly(acrylic acid) (PAA) adsorption layer on the surface of mesoporous-activated carbon HPA obtained by physical activation of residue after supercritical extraction of hops was characterized. This characterization has been done based on the analysis of determination of adsorbed polymer amount, surface charge density, and zeta potential of solid particles (without and in the PAA presence). The SEM, thermogravimetric, FTIR, and MS techniques have allowed one to examine the solid surface morphology and specify different kinds of HPA surface groups. The effects of solution pH, as well as polymer molecular weight and concentration, were studied. The obtained results indicated that the highest adsorption on the activated carbon surface was exhibited by PAA with lower molecular weight (i.e., 2000 Da) at pH 3. Under such conditions, polymeric adsorption layer is composed of nanosized PAA coils (slightly negatively charged) which are densely packed on the positive surface of HPA. Additionally, the adsorption of polymeric macromolecules into solid pores is possible.
机译:在啤酒花超临界萃取后,通过残余物的物理活化获得的介孔活化碳HPA表面的聚丙烯酸(PAA)吸附层的纳米结构被表征。该表征是基于对固体颗粒(不存在和存在PAA的情况下)吸附的聚合物量,表面电荷密度和Zeta电位的测定分析得出的。 SEM,热重,FTIR和MS技术使人们能够检查固体表面形态并指定不同种类的HPA表面基团。研究了溶液pH值以及聚合物分子量和浓度的影响。获得的结果表明,在pH 3下,分子量较低(即2000 Da)的PAA表现出对活性炭表面的最高吸附。在这种条件下,聚合物吸附层由纳米级PAA线圈(带负电荷)组成,紧密堆积在HPA的正表面上。另外,聚合大分子吸附到固体孔中是可能的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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