Correlation of molecular weight diversity and colloidal disability performance of anionic lignin derived polymer

IF 6.3 2区 化学 Q1 POLYMER SCIENCE European Polymer Journal Pub Date : 2025-03-19 Epub Date: 2025-02-10 DOI:10.1016/j.eurpolymj.2025.113820
Farzad Gholami , Weijue Gao , Ehsan Behzadfar , Pedram Fatehi
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Abstract

Polymerization is considered one of the valorization techniques of lignin for various applications. Generally, polymerization techniques affect the molecular structure of polymers. In this work, we evaluated a hypothesis that the polymerization strategy and, thus, the molecular weight distribution of lignin-derived polymers would impact their effectiveness as a colloidal disability agent (i.e., flocculant) for a suspension system. To achieve our goal, different lignin-polymethacrylic acid (PMAA) polymers were synthesized via free radical polymerization (FRP) and atom transfer radical polymerization (ATRP) techniques. The experiments were designed such that two sets of polymers with different molecular polydispersities but similar average molecular weights, charge densities, radii of gyration, and hydrodynamic diameters were obtained. Both systems developed colloidal destabilization mainly via bridging phenomenon. The flocculation performance of the ATRP-synthesized samples with narrower molecular weight distribution was notably better than that of FRP-induced samples. The rheological and flocculation analyses under different shear rates confirmed that the ATRP-induced sample promoted the entanglement of particles and had a higher flocculation efficiency. The flocculant prepared using the ATRP technique demonstrated a significantly lower optimal dosage, requiring only 0.4 mg per gram, compared to 25.6 mg per gram for the samples produced using the FRP method. Also, this sample produced stronger flocs with more re-flocculation tendency under different shear rates, while it generated larger flocs under stirring conditions. Such ATRP-derived flocs had an average chord length of approximately 60 μm, and those of FRP-based ones had a 30 μm chord length, while both FRP and ATRP polymers had 500 Da molecular weight. The results of this work confirmed that, while lignin-derived polymers can be an effective flocculant, strategies must be taken into account for generating lignin-derived polymers with a controlled and preferably narrow molecular weight distribution.

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阴离子木质素衍生聚合物分子量多样性与胶体失能性能的相关性研究
聚合被认为是木质素增值技术之一,具有广泛的应用前景。一般来说,聚合技术影响聚合物的分子结构。在这项工作中,我们评估了一个假设,即木质素衍生聚合物的聚合策略和分子量分布将影响它们作为悬浮系统的胶体失能剂(即絮凝剂)的有效性。为了实现这一目标,采用自由基聚合(FRP)和原子转移自由基聚合(ATRP)技术合成了不同的木质素-聚甲基丙烯酸(PMAA)聚合物。实验设计了两组分子多分散度不同但平均分子量、电荷密度、旋转半径和流体动力直径相似的聚合物。两种体系的胶体失稳主要是通过桥接现象发生的。分子量分布较窄的atrp合成样品的絮凝性能明显优于frp诱导样品。不同剪切速率下的流变学和絮凝分析证实,atrp诱导的样品促进了颗粒的缠结,具有较高的絮凝效率。使用ATRP技术制备的絮凝剂显示出明显较低的最佳用量,仅需要0.4 mg / g,而使用FRP方法生产的样品需要25.6 mg / g。在不同剪切速率下,该样品产生的絮凝体更强,重絮凝倾向更强,而在搅拌条件下,该样品产生的絮凝体较大。ATRP衍生絮凝体的平均弦长约为60 μm, FRP基絮凝体的平均弦长为30 μm,而FRP和ATRP聚合物的分子量均为500 Da。这项工作的结果证实,虽然木质素衍生聚合物可以是一种有效的絮凝剂,但必须考虑到生产木质素衍生聚合物的策略,使其具有可控的和优选的窄分子量分布。
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来源期刊
European Polymer Journal
European Polymer Journal 化学-高分子科学
CiteScore
9.90
自引率
10.00%
发文量
691
审稿时长
23 days
期刊介绍: European Polymer Journal is dedicated to publishing work on fundamental and applied polymer chemistry and macromolecular materials. The journal covers all aspects of polymer synthesis, including polymerization mechanisms and chemical functional transformations, with a focus on novel polymers and the relationships between molecular structure and polymer properties. In addition, we welcome submissions on bio-based or renewable polymers, stimuli-responsive systems and polymer bio-hybrids. European Polymer Journal also publishes research on the biomedical application of polymers, including drug delivery and regenerative medicine. The main scope is covered but not limited to the following core research areas: Polymer synthesis and functionalization • Novel synthetic routes for polymerization, functional modification, controlled/living polymerization and precision polymers. Stimuli-responsive polymers • Including shape memory and self-healing polymers. Supramolecular polymers and self-assembly • Molecular recognition and higher order polymer structures. Renewable and sustainable polymers • Bio-based, biodegradable and anti-microbial polymers and polymeric bio-nanocomposites. Polymers at interfaces and surfaces • Chemistry and engineering of surfaces with biological relevance, including patterning, antifouling polymers and polymers for membrane applications. Biomedical applications and nanomedicine • Polymers for regenerative medicine, drug delivery molecular release and gene therapy The scope of European Polymer Journal no longer includes Polymer Physics.
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