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使用原位生成表面活性剂通过细乳液聚合制备丁苯橡胶

Styrene-Butadiene Rubber by Miniemulsion Polymerization Using In Situ Generated Surfactant.

作者信息

Medeiros Anderson M S, Bourgeat-Lami Elodie, McKenna Timothy F L

机构信息

Univ Lyon, University Claude Bernard Lyon 1, CPE Lyon, CNRS, UMR 5265, Chemistry, Catalysis, Polymers and Processes (C2P2), 43 Bvd. Du 11 Nov. 1918, F-69616 Villeurbanne, France.

出版信息

Polymers (Basel). 2020 Jun 30;12(7):1476. doi: 10.3390/polym12071476.

Abstract

An alternative approach for the synthesis of styrene butadiene rubber (SBR) copolymer latexes was explored in order to obtain low gel fractions and high solid contents. The ultra-turrax-assisted miniemulsion stabilized by in situ surfactant generation was adopted as the main strategy since this technique can inhibit the eventual presence of secondary nucleation producing polybutadiene particles and also control the cross-linking degree. Styrene monomer was first miniemulsified using an ultra-turrax and in situ generated surfactant using either hexadecane (HD) or octadecyl acrylate (ODA) as the hydrophobe. Dynamic light scattering (DLS) measurements of droplet size indicated faster stabilization and the production of smaller droplet diameters ca. 190 nm (PdI = 0.08) when employing in situ generated potassium oleate (K-Oleate) in comparison to SDS-based miniemulsions. High butadiene-level SBR latexes with ca. 50% solids content, a glass transition temperature () of -52 °C, and a butadiene to styrene weight ratio of 75:25, were then obtained using the miniemulsion droplets as seeds. Turbiscan and DLS measurements revealed a very stable resulting latex with SBR particle diameter of ca. 220 nm and a low polydispersity index (PdI). Secondary nucleation was prevented as indicated by the low N/N value. Cryo-TEM images showed a narrow distribution of particle size as well as the absence of agglomeration. The gel content was below 10% when tert-dodecyl mercaptan (t-DM) was used as chain transfer agent (CTA).

摘要

为了获得低凝胶分数和高固含量,探索了一种合成丁苯橡胶(SBR)共聚物胶乳的替代方法。采用原位生成表面活性剂稳定的超高速搅拌辅助细乳液作为主要策略,因为该技术可以抑制最终产生聚丁二烯颗粒的二次成核的存在,并控制交联度。首先使用超高速搅拌将苯乙烯单体细乳化,并使用十六烷(HD)或丙烯酸十八酯(ODA)作为疏水物原位生成表面活性剂。液滴尺寸的动态光散射(DLS)测量表明,与基于十二烷基硫酸钠(SDS)的细乳液相比,使用原位生成的油酸钾(K-油酸盐)时,稳定速度更快,并且产生的液滴直径更小,约为190 nm(多分散指数PdI = 0.08)。然后以细乳液液滴为种子,获得了固含量约为50%、玻璃化转变温度()为-52°C、丁二烯与苯乙烯重量比为75:25的高丁二烯含量SBR胶乳。Turbiscan和DLS测量表明,所得胶乳非常稳定,SBR粒径约为220 nm,多分散指数(PdI)较低。低N/N值表明防止了二次成核。低温透射电子显微镜(Cryo-TEM)图像显示粒径分布狭窄且无团聚现象。当使用叔十二烷基硫醇(t-DM)作为链转移剂(CTA)时,凝胶含量低于10%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b0/7408609/45add451052b/polymers-12-01476-g001.jpg

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