TY - JOUR
T1 - Highly Reactive Biomass Waste Humins Derived from Photocatalytic Polymerization of 5-Hydroxymethylfurfural for Self-Healing Polymers
AU - Zhang, Wenyan
AU - Zhang, Haoyu
AU - Feng, Yirong
AU - Ma, Tingting
AU - Liu, Fengyang
AU - Zhao, Shuangfei
AU - Yang, Jiming
AU - Li, Yuguang
AU - Ji, Dong
AU - Tang, Weiwei
AU - Li, Xiaowei
AU - Fang, Zheng
AU - He, Wei
AU - Guo, Kai
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/3/27
Y1 - 2023/3/27
N2 - In this article, the photocatalytic polymerization of 5-hydroxymethylfurfural (HMF) was applied in the preparation of photo-generated humins (L-H) for the first time. The molecular weight and furan ring content of L-H would be increased by introducing HMF into low-molecular-weight humins (LMW-H) extracted from spoiled HMF under visible light. Compared with humins prepared by the thermal-acid method (A-H), the molecular weight of L-H was less than 800 g/mol; therefore, L-H exhibited great solubility in various solvents and high chemical reactivity for structure modification. Also, the structure units had great differences between L-H and A-H. A-H only consisted of 2,5-dioxo-6-hydroxyhexanal (DHH) and HMF, while L-H also included the 5-hydroxy-4-keto-pentenoic acid (HKPA) generated by reacting HMF with singlet-oxygen. Then, the furan-based polymers were obtained through the classic Diels-Alder (DA) reaction to realize resource utilization of L-H. HKPA units in L-H provided more reaction sites for DA reaction. Characterizations by nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR) spectrum, microscopy, differential scanning calorimetry (DSC), and tensile properties proved that the polymer DA-L-H containing D-A bonds had self-healing properties, and the recovery efficiency could reach 92.8%. Through the utilization of biomass waste humins, the recycling of resources and sustainable economic development could be realized.
AB - In this article, the photocatalytic polymerization of 5-hydroxymethylfurfural (HMF) was applied in the preparation of photo-generated humins (L-H) for the first time. The molecular weight and furan ring content of L-H would be increased by introducing HMF into low-molecular-weight humins (LMW-H) extracted from spoiled HMF under visible light. Compared with humins prepared by the thermal-acid method (A-H), the molecular weight of L-H was less than 800 g/mol; therefore, L-H exhibited great solubility in various solvents and high chemical reactivity for structure modification. Also, the structure units had great differences between L-H and A-H. A-H only consisted of 2,5-dioxo-6-hydroxyhexanal (DHH) and HMF, while L-H also included the 5-hydroxy-4-keto-pentenoic acid (HKPA) generated by reacting HMF with singlet-oxygen. Then, the furan-based polymers were obtained through the classic Diels-Alder (DA) reaction to realize resource utilization of L-H. HKPA units in L-H provided more reaction sites for DA reaction. Characterizations by nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR) spectrum, microscopy, differential scanning calorimetry (DSC), and tensile properties proved that the polymer DA-L-H containing D-A bonds had self-healing properties, and the recovery efficiency could reach 92.8%. Through the utilization of biomass waste humins, the recycling of resources and sustainable economic development could be realized.
KW - Diels−Alder reaction
KW - humins
KW - photocatalytic polymerization
KW - self-healing properties
KW - singlet-oxygen
UR - http://www.scopus.com/inward/record.url?scp=85150438848&partnerID=8YFLogxK
U2 - 10.1021/acssuschemeng.2c06150
DO - 10.1021/acssuschemeng.2c06150
M3 - 文章
AN - SCOPUS:85150438848
SN - 2168-0485
VL - 11
SP - 4595
EP - 4605
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 12
ER -