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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >In situ generation of a self-dispersed beta-nucleating agent with increased nucleation efficiency in isotactic polypropylene
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In situ generation of a self-dispersed beta-nucleating agent with increased nucleation efficiency in isotactic polypropylene

机译:原位产生自分散的β成核剂,具有增加的同位素聚丙烯成核效率

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摘要

Addition of a beta-nucleating agent (beta-NA) is the most effective method of preparing beta-nucleated isotactic polypropylene (beta-iPP); however, the poor dispersion and agglomeration of beta-NAs limit nucleation efficiency. To solve this problem, a self-dispersing beta-NA strategy was developed based on in situ preparation of beta-NA (instead of pre-addition) during the processing of iPP. Zinc adipate (ZnAA), a typical beta-NA, was chosen; self-dispersed ZnAA (ZnAA(IS)) was prepared in situ from its reaction precursors adipic acid (AA) and zinc oxide (ZnO) during extrusion of iPP. In situ preparation of ZnAA(IS) led to a significantly higher nucleation efficiency than pre-addition of ZnAA. The beta-crystal content (k(beta) value) of nucleated iPP prepared with ZnAA(IS) reached 0.99, significantly higher than iPP prepared with ZnAA. Moreover, the impact strength of 0.1 wt % ZnAA(IS)/iPP composites was nearly 5.3-fold higher than neat iPP with a net gain in reinforcement (157%) compared to pre-addition of ZnAA. To explain these phenomena, we proposed mechanism for the self-dispersion of beta-NA in the context of in situ generation of beta-NA during iPP processing; the mechanism was confirmed by Fourier Transform Infrared Spectroscopy (FTIR), Polarized Optical Microscopy (POM), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) data. Therefore, this strategy and method of preparing beta-NA in situ offers unique advantages that will advance the production and application of beta-iPP. Furthermore, this strategy could potentially be extended to solve issues of poor dispersion and agglomeration for other additives. (C) 2018 Elsevier Ltd. All rights reserved.
机译:添加β-成核剂(β-Na)是制备β-核的全丙烯(Beta-IPP)的最有效方法;然而,β-NAS限制成核效率的分散和聚集差。为了解决这个问题,在IPP加工过程中,基于原位制备β-Na(代替预添加)开发了一种自分散的β-NA策略。选择锌己二酸(Znaa),典型的β-Na;在挤出IPP挤出期间,原位制于自分散的Znaa(Zn​​aa(是))原位制于其反应前体酰酸(AA)和氧化锌(ZnO)。原位制备Znaa(IS)导致比加入ZnAA的预核效率明显更高。用Znaa(如)制备的核酸IPP的β-晶体含量(K(β)值达到0.99,显着高于用Znaa制备的IPP。此外,与预加入ZnAA的加固(157%),0.1wt%Znaa(IS)/ IPP复合材料的冲击强度高于纯净IPP的净IPP接近5.3倍。为了解释这些现象,我们在IPP处理期间在原位生成Beta-Na的背景下对Beta-Na的自我分散的机制;通过傅立叶变换红外光谱(FTIR),偏振光显微镜(POM),扫描电子显微镜(SEM)和透射电子显微镜(TEM)数据来确认该机制。因此,这种策略和制备Beta-NA的方法和原位的方法提供了独特的优势,将推进Beta-IPP的生产和应用。此外,这种策略可能会扩展到解决其他添加剂的分散和聚集的问题。 (c)2018年elestvier有限公司保留所有权利。

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