How To Get Isocyanate?

被引:14
作者
Guo, Zhuhua [1 ]
Ding, Xiaoshu [1 ]
Wang, Yanji [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOSGENE-FREE SYNTHESIS; ONE-POT SYNTHESIS; PALLADIUM-CATALYZED CARBONYLATION; DIMETHYL CARBONATE; THERMAL-DECOMPOSITION; OXIDATIVE CARBONYLATION; DIMETHYLHEXANE-1,6-DICARBAMATE; METHOXYCARBONYLATION; NITROBENZENE; UREAS;
D O I
10.1021/acsomega.3c10069
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isocyanate, a pivotal chemical intermediate to synthesize polyurethane with widespread applications in household appliances, automobiles, and construction, is predominantly produced via the phosgene process, which currently holds a paramount status in industrial isocyanate production. Nonetheless, concerns arise from the toxicity of phosgene and the corrosiveness of hydrogen chloride, posing safety hazards. The synthesis of isocyanate using nonphosgene methods represents a promising avenue for future development. This article primarily focuses on the nonphosgene approach, which involves the formation of carbamate through the reaction of nitro-amino compounds with carbon monoxide, dimethyl carbonate, and urea, among other reagents, subsequently leading to the thermal decomposition of carbamate to get isocyanate. This paper emphasizes the progress in catalyst development during the carbamate decomposition process. Single-component metal catalysts, particularly zinc, exhibit advantages such as high activity, cost-effectiveness, and compatibility with a wide range of substrates. Composite catalysts enhance isocyanate yield by introducing a second component to adjust the active metal composition. The central research direction aims to optimize catalyst adaptation to reaction conditions, including temperature, pressure, time, and solvent, to achieve high raw material conversion and product yield.
引用
收藏
页码:11168 / 11180
页数:13
相关论文
共 94 条
[11]   Non-phosgene synthesis of hexamethylene-1,6-diisocyanate from thermal decomposition of hexamethylene-1,6-dicarbamate over Zn-Co bimetallic supported ZSM-5 catalyst [J].
Cao, Yan ;
Chi, Yafang ;
Muhammad, Ammar ;
He, Peng ;
Wang, Liguo ;
Li, Huiquan .
CHINESE JOURNAL OF CHEMICAL ENGINEERING, 2019, 27 (03) :549-555
[12]   Kinetic study of methoxycarbonylation of 1,6-hexanediamine with dimethyl carbonate using Mn(OAc)2 catalyst [J].
Cao, Yan ;
Zhao, Liyan ;
Zhu, Ganyu ;
Wang, Liguo ;
He, Peng ;
Li, Huiquan .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2018, 50 (11) :767-774
[13]   Synthesis of Carbonyl Compounds by Gold-Catalyzed Carbonylation Reactions [J].
Cao, Yanwei ;
He, Lin .
SYNLETT, 2022, 33 (11) :1003-1010
[14]  
Chen D., 2005, CHINESE J CATAL, V26, P57, DOI [10.3321/j.issn:0253-9837.2005.11.013, DOI 10.3321/J.ISSN:0253-9837.2005.11.013]
[15]   One-pot synthesis of 3D-ZIF-7 supported on 2D-Zn-Benzimidazole-Acetate and its catalytic activity in the methoxycarbonylation of aniline with dimethyl carbonate [J].
Dahnum, Deliana ;
Dang, Huyen Tran ;
Tran, Ngoc Tuan ;
Ha, Jeong-Myeong ;
Lee, Hyunjoo .
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, 2021, 99 :380-387
[16]   Phosgene-free synthesis of phenyl isocyanate by catalytic decomposition of methyl N-phenyl carbamate over Bi2O3 catalyst [J].
Dai, Yunsheng ;
Wang, Yue ;
Yao, Jie ;
Wang, Qingyin ;
Liu, Liangming ;
Chu, Wei ;
Wang, Gongying .
CATALYSIS LETTERS, 2008, 123 (3-4) :307-316
[17]  
Dai YS, 2009, CHINESE J CATAL, V30, P1131
[18]   Modeling of Isocyanate Synthesis by the Thermal Decomposition of Carbamates [J].
Dashkin, Ratmir ;
Kolesnikov, Georgii ;
Tsygankov, Pavel ;
Lebedev, Igor ;
Lebedev, Artem ;
Menshutina, Natalia ;
Ghafurov, Khusrav ;
Bagomedov, Abakar .
COMPUTATION, 2020, 8 (04)
[19]  
Deng Y., 2014, Patent No. [US8809574B2, 8809574]
[20]   Competent DNA binder pentagonal bipyramidal Fe(II) complex executed as a proficient catalyst for primary carbamates production from alcohols and urea [J].
Dolai, Malay ;
Pakrashy, Sourav ;
Ghosh, Aloke K. ;
Biswas, Surajit ;
Konar, Saugata ;
Alasmary, Fatmah Ali ;
Almalki, Amani Salem ;
Islam, Md Ataul .
JOURNAL OF MOLECULAR STRUCTURE, 2023, 1274