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用于油/水界面超稳定化的短链和长链几丁质纳米颗粒自组装网络

Self-Assembled Networks of Short and Long Chitin Nanoparticles for Oil/Water Interfacial Superstabilization.

作者信息

Bai Long, Huan Siqi, Xiang Wenchao, Liu Liang, Yang Yang, Nugroho Robertus Wahyu N, Fan Yimin, Rojas Orlando J

机构信息

Bio-Based Colloids and Materials, Department of Bioproducts and Biosystems, Aalto University, Vuorimiehentie1, Espoo 02150, Finland.

Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Jiangsu Key Lab of Biomass-Based Green Fuel and Chemicals, College of Chemical Engineering, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.

出版信息

ACS Sustain Chem Eng. 2019 Apr 1;7(7):6497-6511. doi: 10.1021/acssuschemeng.8b04023. Epub 2019 Mar 3.

Abstract

Highly charged (zeta potential ζ = +105 mV, acetate counterions) chitin nanoparticles (NCh) of three different average aspect ratios (∼5, 25, and >60) were obtained by low-energy deconstruction of partially deacetylated chitin. The nanoparticles were effective in reducing the interfacial tension and stabilized the oil/water interface via network formation (interfacial dilatational rheology data) becoming effective in stabilizing Pickering systems, depending on NCh size, composition, and formulation variables. The improved interfacial wettability and electrosteric repulsion facilitated control over the nanoparticle's surface coverage on the oil droplets, their aspect ratio and stability against coalescence during long-term storage. Emulsion superstabilization (oil fractions below 0.5) occurred by the microstructuring and thickening effect of NCh that formed networks at concentrations as low as 0.0005 wt %. The ultrasound energy used during emulsion preparation simultaneously reduced the longer nanoparticles, producing very stable, fine oil droplets (diameter ∼1 μm). Our findings indicate that NCh surpasses any reported biobased nanoparticle, including nanocelluloses, for its ability to stabilize interfaces at ultralow concentrations and represent a step-forward in efforts to fully replace surfactants in multiphase systems.

摘要

通过对部分脱乙酰化甲壳素进行低能解构,获得了三种不同平均纵横比(约为5、25和>60)的高电荷(ζ电位ζ = +105 mV,醋酸根抗衡离子)甲壳素纳米颗粒(NCh)。这些纳米颗粒在降低界面张力方面很有效,并通过形成网络(界面扩张流变学数据)稳定了油/水界面,从而在稳定皮克林体系方面发挥作用,这取决于NCh的尺寸、组成和配方变量。改善的界面润湿性和电空间排斥有助于控制纳米颗粒在油滴上的表面覆盖率、它们的纵横比以及长期储存期间抗聚结的稳定性。乳液超稳定化(油相分数低于0.5)是由NCh在低至0.0005 wt%的浓度下形成网络的微观结构和增稠效应导致的。乳液制备过程中使用的超声能量同时使较长的纳米颗粒变短,产生了非常稳定的细小油滴(直径约1μm)。我们的研究结果表明,NCh在超低浓度下稳定界面的能力超过了任何已报道的生物基纳米颗粒,包括纳米纤维素,代表了在多相体系中完全替代表面活性剂的努力向前迈出的一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8bf/6448262/648e631cca3b/sc-2018-04023k_0001.jpg

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