Preparation of lignin-based silica composite nanoparticles and its application in HDPE

ZHONG Ruisheng; YANG Dongjie; XIONG Wenlong; GUO Wenyuan; QIU Xueqing

doi:10.11949/j.issn.0438-1157.20150636

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Preparation of lignin-based silica composite nanoparticles and its application in HDPE

更新时间：2025-12-10

- Preparation of lignin-based silica composite nanoparticles and its application in HDPE
- CIESC Journal Issue 8, Pages: 3255-3261(2015)
- 作者机构：
  
  华南理工大学化学与化工学院, 制浆造纸工程国家重点实验室,广东,广州,510640
- 作者简介：
- 基金信息：
- DOI：10.11949/j.issn.0438-1157.20150636
  CLC： 636.2
- Online First：05 August 2015，
  
  Published：05 August 2015
- 稿件说明：
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ZHONG Ruisheng, YANG Dongjie, XIONG Wenlong, et al. Preparation of lignin-based silica composite nanoparticles and its application in HDPE[J]. CIESC Journal, 2015, (8): 3255-3261.
DOI：

ZHONG Ruisheng, YANG Dongjie, XIONG Wenlong, et al. Preparation of lignin-based silica composite nanoparticles and its application in HDPE[J]. CIESC Journal, 2015, (8): 3255-3261. DOI： 10.11949/j.issn.0438-1157.20150636.

摘要

针对目前木质素基SiO2复合纳米颗粒聚集严重及木质素负载量低

难以应用的现状

以碱木质素为主要原料

先通过磷酸化改性制备磷酸化碱木质素

再利用酸析共沉法将1.2份磷酸化碱木质素与1份纳米SiO2(均为质量份)复合制备了木质素-SiO2复合纳米颗粒

并探究复合颗粒对高密度聚乙烯(HDPE)力学性能的影响。FT-IR、XPS、TEM、TG和静态接触角测试结果表明

木质素主要以氢键作用与SiO2结合;与原料二氧化硅相比

复合颗粒的粒径从25 nm增加到40 nm

聚集程度明显减弱;复合纳米颗粒中木质素占47%(质量分数);表面的疏水性增强

有利于复合颗粒在高密度聚乙烯中均匀分散

显著提高了HDPE的拉伸强度。与碱木质素/HDPE复合材料相比

木质素-SiO2复合纳米颗粒/HDPE复合材料的拉伸强度和断裂拉伸率分别提高了48.68%和73.57%。

Abstract

According to the presence situation that lignin-based SiO2 composite nanoparticles are difficult for industry application

owing to serious aggregation and low lignin capacity

phosphatized alkali lignin (PAL) was prepared through phosphorylation reaction using alkali lignin (AL) from the alkaline pulping spent liquor of poplar as main material. The lignin/silica composite nanoparticles (L-SiO2) was combined from 1 part nanosilica with 1.2 part (by mass) synthesized PAL by acidulation co-precipitation method. Subsequently

L-SiO2 was added into HDPE to prepare L-SiO2/HDPE composites. Results of FT-IR

XPS

TEM

TG and static contact angle showed that PAL was bonded to silica through hydrogen bonds. L-SiO2 accounted for 47% (mass) LQA. Compared to crude silica

the particle size of L-SiO2 increased from 25 to 40 nm and the agglomeration of particle decreased noticeably. More importantly

the surface of L-SiO2 became more hydrophobic

which made them disperse better in HDPE. The tensile strength and elongation at break of prepared L-SiO2/HDPE composites were 48.68% and 73.57%

respectively

higher than those of AL/HDPE.

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