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通过光子密度波光谱监测,将乳液聚合放大至100升,聚合物含量高达67重量%。

Scale-up of Emulsion Polymerisation up to 100 L and with a Polymer Content of up to 67 wt%, Monitored by Photon Density Wave Spectroscopy.

作者信息

Jacob Laurence Isabelle, Pauer Werner

机构信息

Institute for Technical and Macromolecular Chemistry, University of Hamburg, Bundesstraße 45, 20146 Hamburg, Germany.

出版信息

Polymers (Basel). 2022 Apr 12;14(8):1574. doi: 10.3390/polym14081574.

Abstract

The scale-up process of the high solid content (up to 67 wt%) emulsion polymerisation of vinyl acetate and Versa10 from 1 L over 10 L to 100 L was investigated. An emulsion copolymerisation of vinyl acetate and neodecanoic acid vinyl ester in a molar ratio of 9:1 was carried out in a starved-fed semi-batch operation. As a radical source, a redox initiator system consisting of L-ascorbic acid, tert-butyl hydroperoxide and ammonium iron (III) sulphate was used. The process parameters, such as the required stirring speed and heat dissipation, were determined and adjusted beforehand via reaction calorimetry to ensure a successful scale-up without safety issues. In addition, the emulsion polymerisation was monitored inline by Raman (qualitative monomer accumulation), as well as Photon Density Wave spectroscopy (particle size and scattering coefficient) and temperature measurements. The data provided by Raman spectroscopy and temperature measurements revealed mixing difficulties due to an insufficient stirring rate, while the inline measurement with Photon Density Wave spectroscopy offered an insight into the development of the product properties. It proved to be reliable and precise throughout the entire scale-up process, especially compared to conventional offline methods, such as dynamic light scattering or sedimentation analysis by means of a disc centrifuge, both of which encountered issues when using higher polymer contents.

摘要

研究了醋酸乙烯酯和Versa10的高固含量(高达67 wt%)乳液聚合从1 L扩大到10 L再到100 L的过程。在饥饿进料半间歇操作中,以9:1的摩尔比进行了醋酸乙烯酯和新癸酸乙烯酯的乳液共聚。作为自由基源,使用了由L-抗坏血酸、叔丁基过氧化氢和硫酸铁(III)铵组成的氧化还原引发剂体系。通过反应量热法预先确定并调整了所需的搅拌速度和散热等工艺参数,以确保成功扩大规模且无安全问题。此外,通过拉曼光谱(定性单体积累)、光子密度波光谱(粒径和散射系数)以及温度测量对乳液聚合进行在线监测。拉曼光谱和温度测量提供的数据显示,由于搅拌速率不足导致混合困难,而光子密度波光谱的在线测量则深入了解了产品性能的发展。在整个扩大规模过程中,它被证明是可靠且精确的,特别是与传统的离线方法相比,如动态光散射或盘式离心机沉降分析,这两种方法在使用较高聚合物含量时都遇到了问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb6/9028448/e78fa8dcad48/polymers-14-01574-g001.jpg

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