A direct functionalization of polyolefins for blend compatibilization by an insertion of 1, 1-bis(phenylsulfonyl)ethylene (BPSE). Issue 24 (21st May 2019)

• Record Type: Journal Article
• Authors: Plummer, Christopher M.; Zhou, Houbo; Li, Sihan; Zhong, Hai; Sun, Ziyang; Bariashir, Chantsalnyam; Sun, Wen-Hua; Huang, Huahua; Liu, Lixin; Chen, Yongming
• Is Part Of: Polymer chemistry. Volume 10:Issue 24(2019)
• Page Start: 3325
• Page End: 3333
• Publication Date: 2019-05-21
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c9py00599d
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : A mild post-modification of polyethylene (PE) & polypropylene (PP) to insert phenylsulfonyl groups is reported, the modified samples demonstrated to act as blend compatibilizers. Abstract : Using recently developed C–H insertion chemistry, a mild post-modification of polyethylene (PE), hyperbranched polyethylene (HBPE) and isotactic polypropylene (iPP) to insert phenylsulfonyl groups was performed. The Michael-type radical addition applies 2-chloroanthroquinone (2-CIAQ) as a C–H bond-cleaving photocatalyst and 1, 1-bis(phenylsulfonyl)ethylene (BPSE) as the olefinic substrate. The reactions were performed in solution with various feed ratios and the products were characterized by multi-instrumental analysis. The modification is a convenient one-step introduction of aromatic moieties along polyolefin chains. By optimization of the reaction conditions, as many as 18.5 graft units of BPSE were introduced per 100 ethylene repeating units. The modified samples were successfully demonstrated to act as a compatibilizer between blends of PE/iPP and polystyrene (PS) as verified by scanning electron microscopy (SEM).