Insight into synergistic antioxidation mechanisms of butyl hydroxyanisole with common synthetic antioxidants

Q2 Agricultural and Biological Sciences
Jun Li , Jiali Chen , Yanlan Bi , Huifang Yang
{"title":"Insight into synergistic antioxidation mechanisms of butyl hydroxyanisole with common synthetic antioxidants","authors":"Jun Li ,&nbsp;Jiali Chen ,&nbsp;Yanlan Bi ,&nbsp;Huifang Yang","doi":"10.1016/j.gaost.2022.06.004","DOIUrl":null,"url":null,"abstract":"<div><p>Butyl hydroxyanisole (BHA) is usually blended with other synthetic antioxidants to improve the antioxidative property due to synergistic antioxidation. However, the synergistic antioxidation mechanisms of BHA with synergists have not been revealed yet. Thus, the antioxidation of BHA with butylated hydroxytoluene (BHT), tert-butylhydroquinone (TBHQ), or propyl gallate (PG) was investigated in the 2,2-azobis(2-amidino-propane) dihydrochloride oxidizing system. The contents of BHA, BHT, TBHQ, PG, and transformation products were measured by high-performance liquid chromatography. Transformation products were identified with liquid chromatography-mass spectrometry and gas chromatography–mass spectrometry. Results showed that synergistic antioxidation occurred between BHA and BHT, TBHQ, or PG. The synergistic antioxidation effect of BHA and BHT was attributed to the regeneration of BHA by BHT. Transformation products of BHA and BHT (compounds 6 and 7, dimers of BHA and BHT) had little contribution due to the relatively low content (&lt;0.6%). The synergistic antioxidation effect of BHA and TBHQ or BHA and PG was attributed to the protective mechanism of TBHQ or PG on BHA. No transformation products were detected of BHA and TBHQ. Transformation products of BHA and PG (compounds 9 and 10, dimers of BHA and PG) had limited contribution due to the relatively low percentage (&lt;7%). Therefore, BHA and BHT performed competitive antioxidation, while BHA and TBHQ or PG performed protective antioxidation.</p></div>","PeriodicalId":33614,"journal":{"name":"Grain Oil Science and Technology","volume":"5 3","pages":"Pages 114-130"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590259822000255/pdfft?md5=8544c941883b8cbf3e47f780c7b7c4eb&pid=1-s2.0-S2590259822000255-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Grain Oil Science and Technology","FirstCategoryId":"1087","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590259822000255","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0

Abstract

Butyl hydroxyanisole (BHA) is usually blended with other synthetic antioxidants to improve the antioxidative property due to synergistic antioxidation. However, the synergistic antioxidation mechanisms of BHA with synergists have not been revealed yet. Thus, the antioxidation of BHA with butylated hydroxytoluene (BHT), tert-butylhydroquinone (TBHQ), or propyl gallate (PG) was investigated in the 2,2-azobis(2-amidino-propane) dihydrochloride oxidizing system. The contents of BHA, BHT, TBHQ, PG, and transformation products were measured by high-performance liquid chromatography. Transformation products were identified with liquid chromatography-mass spectrometry and gas chromatography–mass spectrometry. Results showed that synergistic antioxidation occurred between BHA and BHT, TBHQ, or PG. The synergistic antioxidation effect of BHA and BHT was attributed to the regeneration of BHA by BHT. Transformation products of BHA and BHT (compounds 6 and 7, dimers of BHA and BHT) had little contribution due to the relatively low content (<0.6%). The synergistic antioxidation effect of BHA and TBHQ or BHA and PG was attributed to the protective mechanism of TBHQ or PG on BHA. No transformation products were detected of BHA and TBHQ. Transformation products of BHA and PG (compounds 9 and 10, dimers of BHA and PG) had limited contribution due to the relatively low percentage (<7%). Therefore, BHA and BHT performed competitive antioxidation, while BHA and TBHQ or PG performed protective antioxidation.

Abstract Image

丁基羟基茴香醚与常用合成抗氧化剂协同抗氧化机制的研究
丁基羟基茴香醚(BHA)通常与其他合成抗氧化剂混合使用,通过协同抗氧化来提高抗氧化性能。然而,BHA与增效剂的协同抗氧化机制尚不清楚。因此,在2,2-偶氮双(2-氨基丙烷)盐酸氧化体系中,研究了丁基羟基甲苯(BHT)、叔丁基对苯二酚(TBHQ)或没食子酸丙酯(PG)对BHA的抗氧化作用。采用高效液相色谱法测定BHA、BHT、thbhq、PG和转化产物的含量。转化产物采用液相色谱-质谱联用和气相色谱-质谱联用进行鉴定。结果表明,BHA与BHT、TBHQ、PG之间存在协同抗氧化作用,其协同抗氧化作用与BHT对BHA的再生有关。BHA和BHT的转化产物(化合物6和7,BHA和BHT的二聚体)由于含量相对较低(<0.6%),贡献较小。BHA与thbhq或BHA与PG的协同抗氧化作用归因于thbhq或PG对BHA的保护机制。未检测到BHA和thbhq的转化产物。BHA和PG的转化产物(化合物9和10,BHA和PG的二聚体)由于比例相对较低(<7%),贡献有限。因此,BHA和BHT具有竞争性抗氧化作用,而BHA和thbhq或PG具有保护性抗氧化作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.30
自引率
0.00%
发文量
69
审稿时长
12 weeks
期刊介绍:
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信