Westerman Clayton R, Walker Princess M, Jenkins Courtney L
Department of Chemistry, Ball State University.
Department of Chemistry, Ball State University;
J Vis Exp. 2019 May 20(147). doi: 10.3791/59620.
Elemental sulfur (S8) is a byproduct of the petroleum industry with millions of tons produced annually. Such abundant production and limited applications lead to sulfur as a cost-efficient reagent for polymer synthesis. Inverse vulcanization combines elemental sulfur with a variety of monomers to form functional polysulfides without the need for solvents. Short reaction times and straight forward synthetic methods have led to rapid expansion of inverse vulcanization. However, high reaction temperatures (>160 °C) limit the types of monomers that can be used. Here, the dynamic sulfur bonds in poly(S-divinylbenzene) are used to initiate polymerization at much lower temperatures. The S-S bonds in the prepolymer are less stable than S-S bonds in S8, allowing radical formation at 90 °C rather than 159 °C. A variety of allyl and vinyl ethers have been incorporated to form terpolymers. The resulting materials were characterized by H NMR, gel permeation chromatography, and differential scanning calorimetry, as well as examining changes in solubility. This method expands on the solvent-free, thiyl radical chemistry utilized by inverse vulcanization to create polysulfides at mild temperatures. This development broadens the range of monomers that can be incorporated thus expanding the accessible material properties and possible applications.
元素硫(S8)是石油工业的副产品,每年产量达数百万吨。如此丰富的产量和有限的应用使得硫成为聚合物合成中一种经济高效的试剂。反向硫化将元素硫与多种单体结合,无需溶剂即可形成功能性多硫化物。短反应时间和简单的合成方法导致反向硫化迅速发展。然而,高反应温度(>160°C)限制了可使用的单体类型。在此,聚(S-二乙烯基苯)中的动态硫键被用于在低得多的温度下引发聚合反应。预聚物中的S-S键比S8中的S-S键稳定性更低,使得在90°C而非159°C时就能形成自由基。已引入多种烯丙基醚和乙烯基醚以形成三元共聚物。通过1H NMR、凝胶渗透色谱法、差示扫描量热法对所得材料进行了表征,并研究了溶解度的变化。该方法扩展了反向硫化所采用的无溶剂硫自由基化学,能够在温和温度下制备多硫化物。这一进展拓宽了可引入的单体范围,从而扩大了可获得的材料性能和可能的应用范围。