Suppr超能文献

聚电解质形态和吸附对纳米纤维素絮凝聚的机理的影响。

Effect of polyelectrolyte morphology and adsorption on the mechanism of nanocellulose flocculation.

机构信息

BioResource Processing Research Institute of Australia (BioPRIA), Department of Chemical Engineering, Monash University, Clayton 3800, VIC, Australia; Department of Chemical Engineering, Complutense University of Madrid, Madrid 28040, Spain.

BioResource Processing Research Institute of Australia (BioPRIA), Department of Chemical Engineering, Monash University, Clayton 3800, VIC, Australia; Department of Chemical Engineering, Complutense University of Madrid, Madrid 28040, Spain.

出版信息

J Colloid Interface Sci. 2016 Nov 1;481:158-67. doi: 10.1016/j.jcis.2016.07.048. Epub 2016 Jul 21.

Abstract

The effect of polyelectrolyte morphology, charge density, molecular weight and concentration on the adsorption and flocculation of Microfibrillated Cellulose (MFC) were investigated. Linear Cationic Polyacrylamide (CPAM) and Branched Polyethylenimine (PEI) of varying charge density and molecular weight were added at different dosages to MFC suspensions. The flocculation mechanisms were quantified by measuring gel point by sedimentation, and floc size, strength and reflocculation ability through Focussed Beam Reflectance Measurements. Polymer adsorption was quantified through zeta potential and adsorption measurements using polyelectrolyte titration. The flocculation mechanism of MFC is shown to be dependent on polyelectrolyte morphology. The high molecular weight branched polymer, HPEI formed rigid bridges between the MFC fibres. HPEI had low coverage and negative zeta potential at the optimum flocculation dosage, forming flocs of high strength. After breaking of flocs, total reflocculation was achieved because the high rigidity of polymer did not allow reconformation or flattening of the polyelectrolyte adsorbed on MFC surface. The lower molecular weight branched polymer, LPEI (2kDa) showed rapid total deflocculation, complete reflocculation and had maximum flocculation occurring at the point of zero charge. These characteristics correspond to a charge neutralisation mechanism. However, if the flocculation mechanism was purely charge neutralisation mechanism, the minimum gel point would be at the point of zero charge. Since this is not the case, this difference was attributed to the high polydispersity of the commercial LPEI used, allowing some bridges to be formed by the largest molecules, changing the minimum gel point. With the linear 80% charged 4MDa CPAM, bridging mechanism dominates since maximum flocculation occurred at the minimum gel point, negative zeta potential and low coverage required for maximum flocculation. Reflocculation was not possible as the long linear polymer reconformed on the MFC surface under a flat conformation. Flocculation with the linear 50% charged 13MDa CPAM happened by bridging with the minimum gel point and maximum flocculation corresponding to roughly half polyelectrolyte surface coverage on cellulose.

摘要

研究了聚电解质形态、电荷密度、分子量和浓度对微晶纤维素(MFC)吸附和絮凝的影响。不同电荷密度和分子量的线性阳离子聚丙烯酰胺(CPAM)和支化聚乙烯亚胺(PEI)以不同的剂量添加到 MFC 悬浮液中。通过沉降测量凝胶点、通过聚焦光束反射测量法测量絮体大小、强度和再絮凝能力来定量絮凝机制。通过使用聚电解质滴定法测量zeta 电位和吸附来定量聚合物吸附。结果表明,MFC 的絮凝机制取决于聚电解质形态。高分子量支化聚合物 HPEI 在 MFC 纤维之间形成刚性桥。HPEI 在最佳絮凝剂量下具有低覆盖率和负 zeta 电位,形成高强度絮体。絮体破裂后,由于聚合物的高刚性不允许吸附在 MFC 表面上的聚电解质重新构象或变平,因此可以实现完全再絮凝。低分子量支化聚合物 LPEI(2kDa)表现出快速的完全解絮,完全再絮凝,并且最大絮凝发生在零电荷点。这些特性对应于电荷中和机制。然而,如果絮凝机制纯粹是电荷中和机制,那么最小凝胶点将在零电荷点。由于实际情况并非如此,这种差异归因于所用商业 LPEI 的高多分散性,允许最大分子形成一些桥,从而改变最小凝胶点。对于 80%带电荷的 4MDa 线性 CPAM,桥联机制占主导地位,因为最大絮凝发生在最小凝胶点、形成最大絮体所需的负 zeta 电位和低覆盖率处。由于长线性聚合物在 MFC 表面上重新构象为平面构象,因此无法再絮凝。线性 50%带电荷的 13MDa CPAM 的絮凝是通过桥联作用发生的,最小凝胶点和最大絮凝对应于纤维素上聚电解质表面覆盖率的大致一半。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验