Your browser doesn't support javascript.
loading
Synthesis, Characterization, and Performance Evaluation of Sulfur-Containing Diphenylamines Based on Intramolecular Synergism.
He, Jun-Bo; Shi, Hao; Wang, Yue; Gao, Xin-Lei.
Affiliation
  • He JB; Key Laboratory for Deep Processing of Major Grain and Oil, Ministry of Education, College of Food Science & Engineering, Wuhan Polytechnic University, Wuhan 430023, China. junb112he@whpu.edu.cn.
  • Shi H; Key Laboratory for Deep Processing of Major Grain and Oil, Ministry of Education, College of Food Science & Engineering, Wuhan Polytechnic University, Wuhan 430023, China. go_live@yeah.net.
  • Wang Y; Department of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023, China. yuewang27@163.com.
  • Gao XL; Department of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023, China. gaoxl0131@163.com.
Molecules ; 23(2)2018 Feb 13.
Article in En | MEDLINE | ID: mdl-29438302
ABSTRACT
To obtain novel structural antioxidants that have different antioxidant mechanisms, four 2-(alkylthio)-N-(4-(phenylamino)phenyl)acetamides 2a-d as dual functional antioxidants are designed, synthesized, and confirmed by ¹H-NMR, FTIR, MS, and elemental analysis. The antioxidant behavior of compounds 2a-d as additives of base oil triisodecyl trimellitate (TIDTM) is evaluated by non-isothermal and isothermal DSC analyses. The results showed all compounds can greatly increase the incipient oxidation temperature (IOT) and oxidation induction time (OIT) of TIDTM, especially, compound 2c exhibited an OIT value of 72.5 min at 230 °C, which is almost 28 times the length of TIDTM. Moreover, compounds 2a-d do not affect the tribological performance of TIDTM. The mechanism of antioxidants involved an intramolecular synergism are proposed. This work demonstrates compound 2c can be used as a novel potential antioxidant additive of TIDTM; in addition, it would inspire the emergence of highly potent antioxidants with different antioxidant mechanisms.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sulfur / Diphenylamine / Lubricants / Acetamides / Antioxidants Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sulfur / Diphenylamine / Lubricants / Acetamides / Antioxidants Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2018 Document type: Article Affiliation country: China