Shutong Pang,Hualiang An,Guirong Wang,Xinqiang Zhao,Yanji Wang
Methylcyclohexyl-2,4-diisocyanate (HTDI) is an upgraded product of toluene-2,4-diisocyanate. HTDI-derived polyurethane products show excellent properties such as nonyellowing degeneration, light stability, and weather resistance. The cleavage of dimethyl methylcyclohexyl-2,4-dicarbamate (HTDC) is a crucial step for phosgene-free synthesis of HTDI. In this work, the catalytic performance of ZnO nanoparticles (NPs) with different particle sizes was evaluated for the cleavage of HTDC, and the result showed that the selectivity of HTDI up to 81.3% was achieved with a 94.2% conversion of HTDC over a 19.1 nm ZnO catalyst. It was found from the results of experiments and characterizations that the decrease in ZnO NPs particle size led to the following circumstances: (1) the specific surface area increased, (2) the crystal preferred orientation shifted from the (100) plane to the (002) plane, and (3) the oxygen vacancy concentration increased. The first-principles calculation results showed that two electrons left from the formation of an oxygen vacancy on the ZnO surface could transfer to the neighboring Zn site. Thus, the electron-withdrawing ability of the Zn site is changed and the structure of the ZnO surface is rearranged, which facilitates the inhibition of side reactions. Therefore, changing the concentration of oxygen vacancies and then adjusting the electron-withdrawing ability of Zn sites on the ZnO surface are an effective way to achieve highly selective synthesis of HTDI by the cleavage of HTDC.
Sai Zhang,Khama Rani Ghosh,Zhe Yao,Lingling Li,Anran Qin,Wenqiang Qiao,Zhi Yuan Wang
We report an efficient and phosgene-free method for the synthesis of isocyanate group (NCO)-containing polymers via Lossen rearrangement. The key monomer of N -acetoxymethacrylamide ( AMAA ), possessing N -acetoxy amide (AA) group was synthesized from the reaction of N -hydroxymethacrylamide ( MHA ) with acetic anhydride. By adjusting the feed ratio of methyl methacrylate ( MMA ) and AMAA , a series of AA-containing polymers ( P1-P3 ) were prepared by free-radical polymerization. Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) revealed that the AA groups in polymers P1-P3 can be readily converted to isocyanate groups by heating at 130 ℃ to afford the NCO-containing polymers P4-P6 with conversion percent of 60, 77 and 78, respectively. Furthermore, the AA-containing polymers can be used as a latent NCO-containing polymer for further chemical modification, such as in-situ grafting reaction with hydroxyl compounds. The spectroscopic analyses confirmed that the dye functional group of disperse red 1 (DR1) was successfully grafted on either NCO- or AA-containing polymers.