Controllable degradation of polyurethane elastomer via selective cleavage of CO and CN bonds. (1st March 2018)

• Record Type: Journal Article
• Authors: Wang, Yuqi; Song, Hongyan; Ge, Hui; Wang, Junwei; Wang, Yingxiong; Jia, Shiyu; Deng, Tiansheng; Hou, Xianglin
• Is Part Of: Journal of cleaner production. Volume 176(2018)
• Page Start: 873
• Page End: 879
• Publication Date: 2018-03-01
• Subjects: Controllable degradation -- Selective cleavage -- Coordination catalysis -- Polyurethane elastomer -- Zinc chloride; Factory and trade waste -- Management -- Periodicals; Manufactures -- Environmental aspects -- Periodicals; Déchets industriels -- Gestion -- Périodiques; Usines -- Aspect de l'environnement -- Périodiques; 628.5
• DOI: 10.1016/j.jclepro.2017.12.046
• Languages: English
• ISSNs: 0959-6526

Abstract

Abstract: The degradation and recovery of waste polyurethane materials have confronted enormous challenge. Controllable degradation of polyurethane elastomer is developed via selective cleavage of CO of urethane linkages and CN bonds. It was founded that the selective cleavage of carbon-heteroatom bonds could be efficiently performed in 70% ZnCl2 aqueous solution. The transition metal Zn 2+ coordinated with N and O atoms due to their unshared electron pairs. The CO of urethane linkages and CN bonds were readily cleaved using ZnCl2 as catalysts at 140 °C for 2 h. However, the CC bonds and COC of ether linkages as framework structure remain intact in the degradation process. Eventually, the high-value-added chemicals including 2, 4-diaminotoluene, polytetramethylene ether glycol (PTMEG) and 3, 3′-dichloro-4, 4′-diaminodiphenylmethane (MOCA) were retrieved via selective cleavage of CO of urethane bonds and CN bonds.