Preparation and Characterization of Hyperbranched Silicone Oil by Hydrosilylation Reaction

2013 ◽  
Vol 395-396 ◽  
pp. 363-366
Author(s):  
Zhu Liu ◽  
Hua Shi Liu ◽  
Rui Fang Guan ◽  
Chuan Jian Zhou

Hyperbranched silicone oil was prepared using low-polyhydrosiloxane and vinyl terminated methylphenyl silicone oil as the raw materials through hydrosilylation reaction. The structures and properties of hyperbranched silicone oil were characterized through 1H NMR, TG and dynamic viscosity. The influence on synthesis of hyperbranched silicone oil was discussed, which was caused by ratio of different raw materials. When molar ratio of Si-H bond and Si-Vi bond of raw materials was 3.5:1 (mol), the reaction degree of hyperbranched silicone oils double bond was as high as 80%. At room temperature and 100°C, comparing the dynamic viscosity of hyperbranched silicone oil and straight chain silicone oil, we found that viscosity decrease rate of hyperbranched silicone oil was obviously lower. TG curve of hyperbranched silicone oil and straight chain silicone oil also certified that the hyperbranched silicone oil has higher thermal stability than the straight chain phenyl silicone oil. Therefore hyperbranched silicone oil is more suitable for the preparation of high-performance elastic clay than straight chain silicone oil.

MRS Advances ◽  
2018 ◽  
Vol 4 (07) ◽  
pp. 377-384 ◽  
Author(s):  
DaNan Yea ◽  
SeonHui Jo ◽  
JongChoo Lim

ABSTRACTIn this study, 3 types of zwitterionic phospholipid biosurfactants LDP(S), CDP(S) and CTDP(S) were prepared from 3 different raw materials such as rapeseed oil, coconut oil and cottonseed oil respectively. The structure of the resulting phospholipid biosurfactants was elucidated by FT-IR, 1H NMR and 13C NMR spectroscopies and their interfacial properties have been examined such as CMC, static surface tension, wetting property, solution stability, and foam property. Interfacial property measurement and prescription test in cosmetic formulation prepared with the newly synthesized biosurfactants revealed that CDP(S) biosurfactant possesses excellent mildness and superior interfacial properties, indicating the potential applicability in cosmetic product formulations.


NANO ◽  
2013 ◽  
Vol 08 (04) ◽  
pp. 1350042 ◽  
Author(s):  
JING WANG ◽  
LI GUO ◽  
LI FANG MA

In this paper, we firstly synthesized glycyrrhetinic acid-modified double amino-terminated poloxamer 188 (GA–NH–POLO–NH–GA). The structure of the synthesized compound was confirmed by 1H-NMR and Fourier transform infrared (FT-IR) spectroscopy. Then the nanoparticles composed of GA–NH–POLO–NH–GA/chitosan (GA–NH–POLO–NH–GA/CTS) were prepared by an ionic gelation process. The characterization of the nanoparticles was measured by dynamic light scattering (DLS) and scanning electron microscope (SEM). The results showed that the nanoparticles were well dispersed with a spherical shape and the particle size was distributed between 100 nm and 300 nm. The cytotoxicity based on MTT assay against cells (QGY-7703 cells and L929 cells) showed that the nanoparticles had low toxicity and good biocompatibility. The encapsulation efficiency and drug loading of 5-fluorouracil-loaded nanoparticles (5-FU nanoparticles) were measured by high-performance liquid chromatography (HPLC) and fluorescence spectroscopy, ultraviolet-visible (UV-vis) absorbance. The encapsulation of 5-Fu-loaded CTS nanoparticles was 12.8% and the drug loading was 2.9%, while the encapsulation of 5-Fu-loaded GA–NH–POLO–NH–GA/CTS nanoparticles was 20.9% and the drug loading was 3.36%. The release profile showed that the GA–NH–POLO–NH–GA/CTS nanoparticles were available for sustained release of 5-Fu. The GA–NH–POLO–NH–GA/CTS nanoparticles have a higher affinity to the QGY-7703 cells, so indicated that the GA–NH–POLO–NH–GA/CTS nanoparticles have the capacity of liver-targeting in vitro.


2011 ◽  
Vol 197-198 ◽  
pp. 906-910
Author(s):  
Hui Ru Liu ◽  
Li Qiang Lv ◽  
Xing Chen Zhang

This study concerned a novel super-molecular ionic liquid synthesized by ammonium thiocyanate and caprolactam. The physical characters such as melting point and electric conductivity were investigated. Results showed that the melting point is -12.2°C at the molar ratio of 3:1 (caprolactam/ammonium thiocyanate), which is much lower than raw materials. The electric conductivities of synthesized ionic liquids were close to that of imidazole ILs. The structure of ionic liquid was characterized by IR,1HNMR and quantum chemical calculations. It was shown that the NH4+cation connected with caprolactam organic molecules by hydrogen bonds, leading to the forming of a super-molecular ion. The electrostatic attraction of super-molecular ion with anion was decreased because of the larger volume of super-molecular ion than original cation, thus the melting point decreased. The key properties that distinguish super-molecular ionic liquid from other ILs were the presence of supermolecular ion, which can be used to build up a hydrogen-bonded network. This type ion liquid was named as super-molecular ion liquid.


2019 ◽  
Vol 807 ◽  
pp. 1-10 ◽  
Author(s):  
Guang Xi Xu ◽  
Xiao Tong Sang ◽  
Jing Bao Lian ◽  
Nian Chu Wu ◽  
Xue Zhang

Eu3+ and Tb3+ ions singly activated Gd2O2S hollow spheres have been successfully synthesized via solvothermal method by using Gd (NO3)3, Eu (NO3)3, Tb (NO3)3 and thiourea as raw materials. Detailed characterization of the as-prepared samples were obtained by X-ray diffractometry (XRD), field emission scanning electron microscopy (FE-SEM), transmission electronic microscope (TEM) and photoluminescence (PL) spectroscopy. The results demonstrate that at 220 oC for 24 h, the molar ratio of thiourea/Gd3+ has no significant impact on the phase composition of Gd2O2S products. With the reaction time increased from 6 h to 24 h, the morphology of Gd2O2S samples changed from ellipsoidal to near-spheroidal structure, but still remained hollow structure. PL results show that the strongest emission peaks for Gd2O2S:Eu3+ and Gd2O2S:Tb3+ samples were centered at 625 nm and 545 nm, corresponding to the 5D0→7F2 transition of Eu3+ ions and 5D4→7F5 transition of Tb3+ ions, respectively. The quenching concentrations for Eu3+ and Tb3+ ions were 12% and 6%, which can be attributed to the exchange interaction for Eu3+ and Tb3+ ions, respectively.


2011 ◽  
Vol 295-297 ◽  
pp. 260-263
Author(s):  
Hu Liu ◽  
Bao Song Fu ◽  
Qian Qian Shang ◽  
Guo Min Xiao

For the purpose of combining the properties of polymethylsiloxane and fluorinated compound, hexafluorobutyl mathacrylate (HFBMA) was grafted to polymethylhydrosiloxane (PMHS) by hydrosilylation reaction in the presence of Karstedt’s catalyst. The prepared polymethylsiloxane with pendant fluorocarbon side chains (PMHS-g-HFBMA) was characterized by FTIR, 1H NMR and TGA. The results showed that the expected product was successfully formed. The surface property and solubility of the product were also investigated.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Sunil Kumar Narwal ◽  
Nitin Kumar Saun ◽  
Priyanka Dogra ◽  
Ghanshyam Chauhan ◽  
Reena Gupta

A novel thermotolerant lipase fromBacillus aeriuswas immobilized on inexpensive silica gel matrix. The immobilized lipase was used for the synthesis of biodiesel using castor oil as a substrate in a solvent free system at 55°C under shaking in a chemical reactor. Several crucial parameters affecting biodiesel yield such as incubation time, temperature, substrate molar ratio, and amount of lipase were optimized. Under the optimized conditions, the highest biodiesel yield was up to 78.13%. The characterization of synthesized biodiesel was done through FTIR spectroscopy,1H NMR spectra, and gas chromatography.


2018 ◽  
Vol 25 (5) ◽  
pp. 957-961 ◽  
Author(s):  
Kaiyue Wang ◽  
Huijun Wang ◽  
Yi Zhou ◽  
Guomin Li ◽  
Yaqiao Wu ◽  
...  

AbstractIn this study, the mullite-quartz-based proppants were successfully prepared by using the coal gangue as the raw materials. Then, the effects of the additive and the sintering temperature on the composition, microstructure, and properties of the proppants were investigated. Results showed that the proppants sintered at 1250°C with the 10 wt% bauxite additive presented the best performance, which was very close to that of the quartz-proppant, and met the operational requirements of the 52 MPa coal bed methane wells. The viscous flow mechanism of the liquid phase formed during the sintering process also promoted the arrangement of the grains, thus benefiting the densification and the strength of the proppants.


2014 ◽  
Vol 216 ◽  
pp. 23-28
Author(s):  
Mihai Branzei ◽  
Ionut Cristea ◽  
Ion Ciuca ◽  
Adrian Bibiș ◽  
Marcel Feder

The aim of this paper is quantitative characterization of a MnZn ferrite with Bi2O3increasing addition using the Image-Pro Plus software from Media Cybernetics. The sample matrix is a ferrite with the following chemical composition: Mn0.54Zn0.37Fe2.06O4. We applied the conventional ceramic technology in order to obtain the samples. Thus, the raw materials, i.e. αFe2O3, Mn3O4, and ZnO, in a molar ratio 53:28:19 were mixed in suitable proportions in a steel ball-mill using demineralized water. The mixture was burn off at 800 °C for 1 hour, in air. The pre-sintered powder was milled in steel ball-mill with increasing addition of Bi2O3(0.00, 0.01, 0.03, 0.05, 0.07, 0.10, 0.30, 0.50 wt %). For quick references, the sample without bismuth ions was denoted and the samples with increasing concentrations were numbered from 1, 7.


2011 ◽  
Vol 66-68 ◽  
pp. 65-69
Author(s):  
Long Feng Li ◽  
Yuan Gao ◽  
Mao Lin Zhang

Ca-Mg-Al hydrotalcite-like compounds (CaMgAl-HTLcs) were synthesized by a hydrothermal method, and characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and differential thermal analysis (DTA) techniques. The effects of the medium pH value, the molar ratio of the raw materials, the reaction temperature and the reaction time on the structure of CaMgAl-HTLcs were studied. The results showed that increasing treatment temperature and reaction time could improve the crystallinity and monodispersity of hydrotalcite-like compound particles. And well-defined CaMgAl-HTLcs could be prepared at a pH value of 10~11 with n(Zn+Mg+Ca):n(Al) =2. The products synthesized were applied to PVC to improve the thermal stability of PVC.


Author(s):  
Renita Manurung ◽  
Muhammad Dedi Anggreawan ◽  
Alwi Gery Agustan Siregar

In this research, the bamboo leaf shows promise as an alternative raw material for silica production. This study investigated the performance of heterogeneous catalyst prepared from silica derived bamboo leaf ash after that impregnated with phosphoric acid at ratio various. The catalyst was characterized by X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope Energy Dispersive X-Ray Spectroscopy (SEM-EDS), Brunauer Emmet Teller (BET) and Barrett, Joyner and Halenda (BJH) method and triacetin product analyzed by GC-MS. The optimum condition phosphoric silica catalyst was obtained at phosphoric silica molar ratio of 1:2 and employed in the acetylation of glycerol, respectively. As result, 24 % selectivity for triacetin was obtained in the presence of catalytic amount 5%, molar ratio 1:9 at 100 °C for 4 hours. Bamboo leaf derived phosphoric silica calcined showed high potential to be used as an easy to prepare and high-performance solid catalyst for industrial scale.


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