Kong Fangong, Wang Shoujuan, Gao Weijue, Fatehi Pedram
Key Laboratory of Pulp and Paper Science and Technology of Ministry of Education, China, Qilu University of Technology Jinan 250353 China.
Chemical Engineering Department, Lakehead University Thunder Bay ON P7B 5E1 Canada
RSC Adv. 2018 Mar 29;8(22):12322-12336. doi: 10.1039/c7ra12971h. eCollection 2018 Mar 26.
Kraft lignin (KL) produced in kraft pulping process has a low molecular weight and solubility, which limits its application in industry. For the first time, KL was polymerized with acrylic acid (AA) in an acidic aqueous suspension system to produce a water soluble lignin-AA polymer with a high molecular weight in this work. The polymerization reaction was carried out using KSO as an initiator, and the influence of reaction conditions on the carboxylate group content and molecular weight of resultant lignin polymers was systematically investigated. The mechanism of polymerization of KL and AA was discussed fundamentally. The resulting lignin-AA polymer was characterized by Fourier Transform Infrared spectrophotometry (FTIR), proton nuclear magnetic resonance (H-NMR) and elemental analyses. The results showed that the phenolic hydroxyl group (Ph-OH) content of KL promoted the polymerization under an acidic environment. Under the conditions of 1.5 wt% of initiator, 3.5 of pH, 10.0 of AA/lignin molar ratio, 0.15 mol L of lignin concentration, 3 h and 80 °C, the carboxylate group content and the molecular weight of the polymer were 7.37 mmol g and 7.4 × 10 g mol, respectively. The lignin-AA polymer was water soluble at a 10 g L concentration and a pH higher than 4.5. Furthermore, the flocculation performance of lignin-AA polymer in an aluminium oxide suspension was evaluated. Compared with polyAA, the lignin-AA polymer was a more efficient flocculant for aluminium oxide suspension, which shows its potential to be used as a green flocculant in industry.
硫酸盐法制浆过程中产生的硫酸盐木质素(KL)分子量低且溶解性差,这限制了其在工业中的应用。在本研究中,首次在酸性水悬浮体系中使KL与丙烯酸(AA)聚合,以制备具有高分子量的水溶性木质素-AA聚合物。使用KSO作为引发剂进行聚合反应,并系统研究了反应条件对所得木质素聚合物羧基含量和分子量的影响。从根本上探讨了KL与AA的聚合机理。通过傅里叶变换红外光谱法(FTIR)、质子核磁共振(H-NMR)和元素分析对所得木质素-AA聚合物进行了表征。结果表明,KL的酚羟基(Ph-OH)含量在酸性环境下促进了聚合反应。在引发剂含量为1.5 wt%、pH为3.5、AA/木质素摩尔比为10.0、木质素浓度为0.15 mol/L、反应时间为3 h和反应温度为80℃的条件下,聚合物的羧基含量和分子量分别为7.37 mmol/g和7.4×10 g/mol。木质素-AA聚合物在浓度为10 g/L且pH高于4.5时可溶于水。此外,还评估了木质素-AA聚合物在氧化铝悬浮液中的絮凝性能。与聚AA相比,木质素-AA聚合物是一种更高效的氧化铝悬浮液絮凝剂,显示出其在工业中用作绿色絮凝剂的潜力。