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POLYMERIZABILITY OF ALIPHATIC CYCLIC ESTERS

机译:脂族环酯的聚合性

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摘要

The fundamental factors influencing polymerizability of aliphatic cyclic esters(lactones,lactides and carbonates - see Scheme A)were discussed on the basis of literature review.Thermodynamic factors(a)related mostly to the monomer ring strain and the numbers of degrees of freedom of the polymer repeating units as well as kinetic factors(b)resulting from the polymerization mechanism availability securing the sufficient polymerization rate were distinguished.An attention was paid to the fact that thermodynamically determined inability of cyclic ester to polymerize was not tantamount to its inability to ring-opening reaction.The syntheses of macromolecular copolymers containing up to 50-mole % of repeated units coming from non-homopolymerizable monomer are possible.The analysis of kinetic factors allowed concluding that there was no uniform correlation between monomer reactivity and ring size.Moreover,dependently on the polymerization mechanism,the reversed reactivity order could occur.The methods of polymer yield increasing,in connection with disadvantageous occurring(in some cases)of substantial equilibrium concentrations of monomer and cyclic oligomers were also discussed.
机译:在文献综述的基础上讨论了影响脂族环状酯(内酯,丙交酯和碳酸酯-参见方案A)的可聚合性的基本因素。热力学因素主要与单体环应变和单体的自由度数有关。区分了聚合物重复单元以及由确保足够聚合速率的聚合机理可得性引起的动力学因素(b)。要注意以下事实:热力学确定的环状酯的聚合能力不等于其不能环化。可以合成最多50摩尔%的不可共聚单体的重复单元的大分子共聚物。动力学因素的分析可以得出结论,单体反应性和环大小之间没有统一的相关性。在聚合机理上,可能发生相反的反应顺序。还讨论了提高聚合物收率的方法,以及在某些情况下不利地发生的单体和环状低聚物基本平衡浓度的问题。

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