期刊
POLYMER TESTING
卷 104, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.polymertesting.2021.107389
关键词
Hydroxyl-terminated polybutadiene derivatives; Post-polymerization modification; Anionic polymerization; Thiol-ene reaction; Polyurethane elastomer
资金
- National Natural Science Foundation of China [51803111]
- Foundation of Key Laboratory of Pulp and Paper Science and Technology of Ministry of Education of China [KF201922]
- Open Project of Shaanxi Key Laboratory of Macromolecular Science and Technology
- Major scientific and technological innovation projects of Shandong Province [2019JZZY020230]
The use of hydroxy-terminated oligomers with narrow molecular weight distribution as the soft segment of polyurethane enhances the mechanical properties of polyurethane. Different side-chain derivatives of hydroxyl-terminated polybutadiene (HTPB) were successfully synthesized, impacting properties such as glass transition temperature and viscosity. The introduction of side chains in the backbone of HTPB affects the tensile strength and elongation at break of polyurethane elastomers, with varying results based on the length of the side chain.
Hydroxy-terminated oligomers with narrow molecular weight distribution using as soft segment of polyurethane can significantly increase the modulus, tensile strength, and elongation at break of the polyurethane. Thus, design and synthesis of new hydroxy-terminated oligomers having narrow molecular weight distribution can improve the properties of polyurethane and further expand the use range of polyurethane. A set of side-chain hydroxyl-terminated polybutadiene (HTPB) derivatives were successfully synthesized by anionic polymerization and blue light photocatalytic thiol-ene reaction. Firstly, HTPB with narrow molecular weight distribution was synthesized via anionic polymerization using mono-lithium based initiator and followed by de-protection. Then, HTPB derivatives with different side-chains such as butyl, ethyl acetate, or myristyl, namely HTPBbut, HTPB (eac) and HTPBtet, were obtained by blue light photocatalytic thiol-ene reaction using Ru(bpy)(3)Cl-2 as photoredox catalyst and HTPB as matrix polymer. Similar with HTPB, those HTPB derivatives also have narrow molecular weight distribution. Polyurethane elastomers (PUs) were synthesized with HTPB or HTPB derivatives as soft segment, toluene diisocynate (TDI) as hard segment, and 1, 4-butanediol as chain extender. Compared study the performances of polymers, the results showed that glass transition temperature (T-g) and viscosity of HTPB derivatives were increased when short-chain side groups were introduced. But instead, T-g and viscosity of HTPB derivatives was reduced following long-chain side groups being grafted. Through comparing research of properties for PUs, tensile strength is reduced and elongation at break is augmented, when side groups were introduced in HTPB backbone. Research on the contact angle tests of PUs indicated that the contact angle of PUs using HTPB, HTPBbut or HTPBeac as soft segment, is similar, and PUs using HTPBtet as soft segment has a larger contact angle about 137.2 degrees C.
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