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纸质出版日期:2010-2-20,
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马庆伟, 秦玉升, 赵晓江, 王献红, 王佛松. 聚碳酸1,2-丙二酯的碱催化水解研究[J]. 高分子学报, 2010,(2):217-221.
MA Qingwei, QIN Yusheng, ZHAO Xiaojiang, WANG Xianhong, WANG Fosong. BASE CATALYZED HYDROLYSIS OF POLY(PROPLENE CARBONATE)[J]. Acta Polymerica Sinica, 2010,(2):217-221.
马庆伟, 秦玉升, 赵晓江, 王献红, 王佛松. 聚碳酸1,2-丙二酯的碱催化水解研究[J]. 高分子学报, 2010,(2):217-221. DOI: 10.3724/SP.J.1105.2010.00217.
MA Qingwei, QIN Yusheng, ZHAO Xiaojiang, WANG Xianhong, WANG Fosong. BASE CATALYZED HYDROLYSIS OF POLY(PROPLENE CARBONATE)[J]. Acta Polymerica Sinica, 2010,(2):217-221. DOI: 10.3724/SP.J.1105.2010.00217.
研究了高分子量聚碳酸1
2-丙二酯的碱催化水解反应,并通过核磁共振谱仪和气相色谱质谱联用仪对降解反应产物的解析,发现碱催化聚碳酸1
2-丙二酯水解是无规断链反应和解拉链反应共同作用的结果.结果表明高分子量聚碳酸1
2-丙二酯的碱催化水解是制备低分子量聚碳酸1
2-丙二酯的方法之一.
The base catalyzed hydrolysis reaction of poly(propylene carbonate) (PPC)
a highly alternative copolymer synthesized from carbon dioxide and propylene oxide
was investigated systematically in this report.The influences of reaction time
concentration of PPC solution
concentration of base (sodium hydroxide) solution
and residual zinc oxide on the degradation reaction were discussed.1H-NMR spectra were used to analyze the carbonate unit content in the degraded polymer
it was found that the carbonate unit in the final degraded polymer maintained above 80% for all the studied conditions.The number average molecular weight of the final polymer dropped very quickly in the first several hours
a 50% decrease was observed in the first 2~6 h
depending on the concentration of PPC.The higher concentration of PPC was
the slower the decrease in molecular weight
when the concentration of PPC was 0.1 g/L
the number average molecular weight of the final polymer was 18500 after 8 h at 50℃
whereas it was 33700 when the PPC concentration was 0.5 g/L.Degradation time and base concentration were the two important factors for the yield as well as carbonate unit content in the degraded polymer
when the base concentration was 0.25 mol/L
the polymer yield maintained above 90% with carbonate unit over 80% at 48 h
the polymer yield dropped to ca.60% when the base concentration increased to 2.0 mol/L.Generally
prolonged degradation time caused yield loss in the final polymer
and the degradation reaction was enhanced with increasing base concentration.Compared with the purified PPC sample
the existence of zinc oxide in the as-polymerized PPC led to more severe degradation reaction.The GC-MS spectra were used to analyze the liquid compounds of the degraded products
where 1
2-isopropane-diol and propylene carbonate were detected
therefore
it was concluded that the random degradation reaction dominated in the base catalyzed degradation reaction at first stage
however
the unzipping degradation reaction became dominant with the degradation reaction proceeding
a preliminary mechanism for base catalyzed PPC degradation was proposed.Since the base catalyzed degradation can stably produce low molecular weight PPC under controlled conditions
this reaction was therefore considered as a new method to prepare low molecular weight PPC
with number average molecular weight adjustable from 4000 to 10000
聚碳酸1碱催化水解低分子量聚碳酸12-丙二酯
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