RAFT Polymerization of a Biorenewable/Sustainable Monomer via a Green Process

被引:13
|
作者
Versteeg, Friso G. [1 ]
Hegeman, Niels C. [1 ]
Sebakhy, Khaled O. [1 ]
Picchioni, Francesco [1 ]
机构
[1] Univ Groningen, Dept Chem Engn Prod Technol, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
关键词
alpha-Methylene-gamma-butyrolactone; biorenewables; glass transition (T-g); RAFT; supercritical CO2; sustainability; SUPERCRITICAL CARBON-DIOXIDE; RADICAL POLYMERIZATION; POLYMERS; BUTYROLACTONE; ARCHITECTURE; TEMPERATURE; COPOLYMERS; EMULSION; STYRENE;
D O I
10.1002/marc.202200045
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A biorenewable polymer is synthesized via a green process using the RAFT principle for the first time in supercritical CO2 at 300 bar and 80 C. alpha-Methylene-gamma-butyrolactone polymers of various chain lengths and molecular weights are obtained. The molecular weights vary from 10 000 up to 20 000 with low polydispersity indexes (PDI <1.5). Furthermore, the monomer conversion in supercritical CO2 is substantially higher, respectively 85% for ScCO2 compared to approximate to 2,65% for polymerizations conducted in dimethyl formamide (DMF) solvent. Chain extensions are carried out to confirm the livingness of the formed polymers in ScCO2. This opens up future possibilities of the formation of different polymer architectures in ScCO2. The polymers synthesized in ScCO2. have glass transition temperature (T-g) values ranging from 155 up to 190 degrees C. However, the presence of residual monomer encapsulated inside the formed polymer matrix affects the glass transition of the polymer that is lowered by increasing monomer concentrations. Hence, additional research is required to eliminate the remaining monomer concentration in the polymer matrix in order to arrive at the optimal T-g.
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页数:7
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