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首页> 外文期刊>Macromolecules >A kinetic investigation of seeded emulsion polymerization of styrene using reversible addition-fragmentation chain transfer (RAFT) agents with a low transfer constant
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A kinetic investigation of seeded emulsion polymerization of styrene using reversible addition-fragmentation chain transfer (RAFT) agents with a low transfer constant

机译:使用低转移常数的可逆加成-断裂链转移(RAFT)试剂对苯乙烯进行种子乳液聚合的动力学研究

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The mechanisms were investigated for the seeded emulsion polymerization of styrene mediated by xanthate-based reversible addition-fragmentation chain transfer (RAFT) agents with low transfer constants (ca. 0.7). gamma-Radiolysis relaxation measurements were used to determine the exit rate coefficient directly; this increased with the amount of RAFT, consistent with the chain-transfer characteristics of RAFT and the standard transfer/diffusion mechanism for exit. Combining the exit data with measurements of the steady-state rate with chemical initiation showed that the entry rate coefficients decreased with the amount of RAFT, while with gamma initiation the entry rate coefficients were unaffected, unless a very high RAFT concentration was used. This behavior is inconsistent with conventional assumptions about RAFT and the aqueous-phase propagation model for entry (which predicts the entry rate coefficient successfully for ordinary emulsion polymerization systems). It is postulated that the RAFT agents used in this work are surface active, which is not unexpected given the canonical forms of these RAFT agents. The dramatic decrease in entry rate coefficient for the chemically initiated system can be taken into account within the framework of the standard aqueous-phase model for entry if it is assumed that the surface activity gives an increased concentration of RAFT near the surface, which leads to increased transfer to radicals which desorb instead of entering, and whose subsequent reentry is "frustrated" by this event recurring, until they eventually undergo aqueous-phase termination. [References: 42]
机译:研究了由黄原酸酯基可逆加成-断裂链转移(RAFT)剂介导的低转移常数(约0.7)的苯乙烯种子乳液聚合的机理。伽马射线分解弛豫测量直接用于确定出口速率系数。随RAFT的增加而增加,这与RAFT的链转移特性和出口的标准转移/扩散机制相一致。将出口数据与稳态速率与化学引发的测量值结合起来显示,进入速率系数随RAFT的量而降低,而对于伽马射线引发,除非使用非常高的RAFT浓度,否则进入速率系数不受影响。此行为与有关RAFT的常规假设和进入的水相传播模型(它成功地预测了普通乳液聚合体系的进入速率系数)不一致。据推测,在这项工作中使用的RAFT剂具有表面活性,鉴于这些RAFT剂的规范形式,这并不意外。如果假设表面活性使表面附近的RAFT浓度增加,则可以在标准水相模型的框架内考虑化学引发体系的进入速率系数的急剧下降。增加转移到解吸而不是进入的自由基上,并且由于该事件的反复发生,随后的折返被“挫败”,直到它们最终经历水相终止。 [参考:42]

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