Synthesis and chromatographic evaluation of phenyl/tetrazole bonded stationary phase based on thiol-epoxy ring opening reaction

2018 ◽  
Vol 41 (4) ◽  
pp. 856-867 ◽  
Author(s):  
Gaowa Jin ◽  
Yanming Liu ◽  
Fan Yang ◽  
Dongping Yu ◽  
Jingyu Yan ◽  
...  
2011 ◽  
Vol 337 ◽  
pp. 184-187
Author(s):  
Gui Xiang Hou ◽  
Xiao Ai Chen ◽  
Xiao Ming Sang

Epoxy resin/polymethyl methacrylate(EP/PMMA,70/30) interpenetrating network composites containing various contents of dimethyl sulfoxide modified kaoline (EP/PMMA /K-DMSO) composites were prepared by a sequential polymeric technique and an in situ intercalation method. FTIR results showed that the epoxy ring opening reaction occurs, the formation of IPN structure of PMMA and EP has been created. The structure of composite material was characterized by scanning electronic microscopy (SEM). The result indicated that higher impact strength and lower tensile strength with increasing concentration of K-DMSO.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Jing Zhang ◽  
Ji Jun Tang ◽  
Jiao Xia Zhang

Several biorenewable vegetable oil-based polyols with different molecular weights and various hydroxyl functionalities were successfully prepared by ring-opening epoxidized soybean oil with a castor oil-based fatty diol. It was found that several factors, including reaction time, reaction temperature, and molar ratios between epoxidized soybean oil and castor oil diol, affect structures and rheology behaviors of the final polyols. Proton NMR, FT-IR, GPC, and rheometry results revealed that the hydroxyl functionalities, molecular weight, and viscosity of the polyols could be tailored by controlling the above-mentioned factors. Besides, the role of solvents in the epoxy ring-opening process was investigated as well.


2019 ◽  
Vol 36 (3) ◽  
pp. 1165-1173 ◽  
Author(s):  
Kaline A. Wanderley ◽  
Amanda M. Leite ◽  
Gabriel Cardoso ◽  
Anderson M. Medeiros ◽  
Caroline L. Matos ◽  
...  

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 350 ◽  
Author(s):  
Alina Pruna ◽  
Alfonso Cárcel ◽  
Adolfo Benedito ◽  
Enrique Giménez

Low-density three-dimensional (3D) N-doped graphene aerogels by a one-step solvothermal method in the presence of ethylenediamine (EDA) are reported. The gelation, formation, and properties of the aerogels were studied with solvothermal conditions, namely, operating temperature, time, graphene oxide (GO) concentration, and the GO/EDA w/w ratio. Two ranges of solvothermal conditions are employed: one involving an operating temperature below 100 °C and a conventional chemical reduction of GO with EDA at atmospheric pressure and a second one employing a higher temperature range up to 165 and a high pressure reduction with EDA. The results show that both solvothermal approaches allow for the fabrication of homogeneous N-doped 3D graphene aerogels with density values close to 10 mg cm−3. The measurements indicated that low values of GO concentration, temperature, and EDA are optimum for obtaining low-density 3D aerogels. N doping is improved with an EDA amount in lower temperature conditions. The N doping mechanism below 100 °C is dominated by the epoxy ring opening while at temperatures up to 165 °C both epoxy ring opening and amidation take place. The CO2 adsorption properties are strongly controlled by the nitrogen configuration, namely, pyridinic nitrogen in terms of its density.


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