Fluorinated natural rubber with enhanced strength and excellent resistance to ozone, organic solvent, and acid and alkali via in situ reactive melt extrusion
{"title":"Fluorinated natural rubber with enhanced strength and excellent resistance to ozone, organic solvent, and acid and alkali via in situ reactive melt extrusion","authors":"Shijiang Zhu, Fuchun Zhao, Yikang Sun, Chunlin Wang, Zhonghua Yuan, Shuangquan Liao","doi":"10.1016/j.polymdegradstab.2024.110916","DOIUrl":null,"url":null,"abstract":"<div><p>Natural rubber (NR), as a green and renewable industrial raw material, is applied in many fields. However, the relatively weak resistance originated from its unsaturated backbone structure restricts the further application in some harsh conditions. To incorporate the excellent resistance feature of the fluorinated components into NR, fluorinated natural rubber (FNR) was prepared with dodecafluoroheptyl methacrylate (DFHMA) via <em>in situ</em> melt extrusion reaction. The results indicated that fluorinated reaction of NR mainly happened at the α-H of double bond in backbone chain and that styrene could promote fluorination and increase the size of fluorinated side chain. The vulcanized FNR (VFNR) exhibited wonderful mechanical performance, remarkable hydrophobicity, and excellent resistance to ozone, organic solvent, acid and alkali. The water contact angles of VFNR increased from 89 ° to 104 °and the ozone aging cracking time of VFNR increased by one time longer than that of VNR. The swelling degree of VFNR in the full synthetic engine oil is only two-thirds that of VNR, and the retention of tensile strength after immersion in HCl, H<sub>2</sub>SO<sub>4</sub>, and NaOH solution was elevated by 13 %, 11 %, and 5 % compared to those of VNR, respectively. This work presents a simple and eco-friendly method to prepare the fluorinated natural rubber facilitating the industrial fabrication of green and high-performance NR via melt extrusion.</p></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":null,"pages":null},"PeriodicalIF":6.3000,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S014139102400260X","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Natural rubber (NR), as a green and renewable industrial raw material, is applied in many fields. However, the relatively weak resistance originated from its unsaturated backbone structure restricts the further application in some harsh conditions. To incorporate the excellent resistance feature of the fluorinated components into NR, fluorinated natural rubber (FNR) was prepared with dodecafluoroheptyl methacrylate (DFHMA) via in situ melt extrusion reaction. The results indicated that fluorinated reaction of NR mainly happened at the α-H of double bond in backbone chain and that styrene could promote fluorination and increase the size of fluorinated side chain. The vulcanized FNR (VFNR) exhibited wonderful mechanical performance, remarkable hydrophobicity, and excellent resistance to ozone, organic solvent, acid and alkali. The water contact angles of VFNR increased from 89 ° to 104 °and the ozone aging cracking time of VFNR increased by one time longer than that of VNR. The swelling degree of VFNR in the full synthetic engine oil is only two-thirds that of VNR, and the retention of tensile strength after immersion in HCl, H2SO4, and NaOH solution was elevated by 13 %, 11 %, and 5 % compared to those of VNR, respectively. This work presents a simple and eco-friendly method to prepare the fluorinated natural rubber facilitating the industrial fabrication of green and high-performance NR via melt extrusion.
期刊介绍：
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.
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