Hong Yin

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Name: 尹红; Hong Yin
Organization: Zhejiang University
Department:
Title: Associate Professor
Co-reporter:Gang Wang, Hong Yin, Shenfeng Yuan, Zhirong Chen
Journal of Analytical and Applied Pyrolysis 2017 Volume 124(Volume 124) pp:
Publication Date(Web):1 March 2017
DOI:10.1016/j.jaap.2017.02.017
•The formation rate of carbonaceous substances was firstly estimated with Voorhies formula.•The effect of diluent N2 on formation rate of carbonaceous substances was firstly discussed.•The Voorhies formula was firstly modified in the presence of diluent N2.•The parameter in Voorhies formula and modified Voorhies formula was determined.•The formation rate of carbonaceous substances could be effectively predicted.A simple and effective empirical method for carbonaceous substances production estimation and the effect of diluent N2 on it during pyrolysis of trifluoromethane (R23) was firstly studied at the temperatures of 973 K to 1223 K and residence times of 4 s to 40 s. The products were identified and quantified by using GC–MS and GC-FID respectively. The production of carbonaceous substances could be expressed as Voorhies formula of Cn = Atn and the parameter n was approximately constant as 0.67, while A could be expressed with pyrolysis temperature as A = 4537 × exp (−1.58 × 104/T) through simulating the experimental data from 973 K to 1173 K. The production of carbonaceous substances at temperature of 1223 K and residence times from 4 s to 9 s could be effectively predicted by using experiential formula of Cn = 4537 × exp (−1.58 × 104/T) × t0.67, while in the presence of diluent N2, it could be effectively predicted by using Voorhies formula modified with dilution ratio γ as C’n = 4537 × exp (−1.58 × 104/T − 0.52 × γ) × t0.67, which could be considered and used for reference in other pyrolysis process.
Co-reporter:Zhirong Chen, Weitao Yang, Hong Yin, Shenfeng Yuan
Chinese Journal of Chemical Engineering 2017 Volume 25, Issue 10(Volume 25, Issue 10) pp:
Publication Date(Web):1 October 2017
DOI:10.1016/j.cjche.2017.03.012
The uncatalyzed reaction of p-tolyl isocyanate (p-TI) with water in N,N-dimethylformamide (DMF) was investigated by high performance liquid chromatography (HPLC). The reactions were carried out at different temperatures from 293 K to 323 K, using various molar ratios of water to p-TI. DMF, as a special amide, was proved to be an efficient catalyst for water–isocyanate reaction. Under the reaction conditions in this study, substituted urea was the only final product observed. An appreciable amount of intermediate p-toluidine was detected. Concentrations of the isocyanate group as well as the amine and urea were determined as a function of time. New kinetic equations were deduced for each of the substance on the basis of a multistep mechanism, instead of a simple second order reaction as usual. Kinetic constants were calculated using the software MATLAB. Furthermore, the effects of temperature and concentrations of reactants on the reaction rate and amine content were discussed. The activation energy of each step was also determined.
Co-reporter:Shenfeng Yuan;Shuangfeng Jin;Zhirong Chen;Yanna Yuan
Chemical Engineering & Technology 2014 Volume 37( Issue 12) pp:2165-2174
Publication Date(Web):
DOI:10.1002/ceat.201300873

Abstract

The drop size is of fundamental importance in the design of liquid-liquid extraction columns, the drop size was measured as a function of the geometry, operating conditions, and physical properties of a liquid-liquid system with no mass transfer in a five-stage modified Scheibel extraction column. An improved correlation of the mean drop size in the Scheibel extraction column is presented. The correlation was divided into three sections in terms of the Reynolds number. It could be applied in a wide range and could be further used for the study of mass transfer performance of the modified Scheibel extraction column.

Co-reporter:Hangjun Deng;Zhongquan Shen;Lifeng Li;Jizhong Chen
Journal of Applied Polymer Science 2014 Volume 131( Issue 15) pp:
Publication Date(Web):
DOI:10.1002/app.40503

ABSTRACT

The polymerization of tetrahydrofuran (THF) was carried out in CH2Cl2 by using phosphotungstic heteropolyacid as initiator and epichlorohydrin as promoter. This cationic ring-opening polymerization process was monitored by in situ mid-infrared spectroscopy system (ReactIR) to further study the thermodynamics and kinetics of THF polymerization. It was observed that the sharp infrared peak of COC stretching vibrations will shift from about 1068 to 1109 cm−1 in THF ring-opening step. The changes in absorbance intensity of the two characteristic peaks were used for determining instantaneous concentration of linear polymer and ring monomer. The experimental results demonstrated that the kinetics of THF polymerization proved to be typically first-order. Thermodynamic parameters were determined from the temperature dependence of the monomer equilibrium concentration [M]e over the range from −5 to 25°C. The values of kapp were obtained via the plots of ln{([M]0−[M]e)/([M]t−[M]e)} vs reaction time, for polymerization under specific conditions. The apparent activation energy (Ea) and frequency (A) were determined from the Arrhenius plot of kapp vs. T−1. Besides, the in situ kinetic investigation revealed that more chain-transfer occurred at higher temperatures, leading to a reduction in propagation species concentration and a deviation from first-order propagation at the later stage of polymerization. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40503.

Co-reporter:Shenfeng Yuan;Wendong Yang;Zhirong Chen
Journal of Chemical Technology and Biotechnology 2013 Volume 88( Issue 8) pp:1523-1528
Publication Date(Web):
DOI:10.1002/jctb.3997

Abstract

Background

Acetone and tetrahydrofuran are commonly used as solvents in the chemical industry. The separation of acetone–tetrahydrofuran mixtures is often faced in the pharmaceutical and special chemical industries. As acetone and tetrahydrofuran can form a minimum azeotrope, they cannot be separated by conventional distillation. But acetone and tetrahydrofuran are important organic raw materials and solvents, so the mixture should be separated for reuse.

Results

The process of continuous extractive distillation was used to separate the mixture of acetone (62% mass fraction) and tetrahydrofuran (38% mass fraction) using butyl ether as solvent. The characteristics of the continuous extractive distillation were simulated via ASPEN and experiments also showed the feasibility of separating the acetone–tetrahydrofuran mixture. Effects of the reflux mass ratio (R), mixture feed stage (FS), the solvent feed stage (SFS) on the extractive distillation column and the volume ratio of solvent to mixture (S/F) on the distillate mass fraction of acetone and bottom product mass fraction of acetone were investigated. The results of the extractive distillation simulation were verified by experiment data. With the following operation conditions for the extractive distillation column: number of theoretical plates 53; mixture feed at 24th plate; solvent feed at 7th plate, solvent to mixture ratio 3 and reflux mass ratio 3, the mass fraction of acetone in the distillate can reach 99%.

Conclusions

The process of continuous extractive distillation using butyl ether as solvent can separate the acetone–tetrahydrofuran mixture. The solvent to mixture ratio and reflux mass ratio are important factors that affect the mass fraction of the product. © 2013 Society of Chemical Industry

Co-reporter:S. Yuan;Y. Shi;H. Yin;Z. Chen ;J. Zhou
Chemical Engineering & Technology 2012 Volume 35( Issue 10) pp:1810-1816
Publication Date(Web):
DOI:10.1002/ceat.201100470

Abstract

Experiments were designed to ascertain the main factors for the Sauter mean drop size (d32) of the dispersed phase in a three-stage modified Scheibel extraction column with no mass transfer. A precise correlation applied to the liquid-liquid systems with low interfacial surface tension was proposed for calculating d32. The maximum relative error for all data was 16.0 % and the mean relative error ±4.6 %.

Co-reporter:Zhi-Zheng Liu;Zhi-Rong Chen;Shen-Feng Yuan
Chemical Papers 2012 Volume 66( Issue 11) pp:1059-1064
Publication Date(Web):2012 November
DOI:10.2478/s11696-012-0205-8
Reaction mechanism of 1,1,1-trifluorotrichloroethane (CF3CCl3) and sulphur trioxide (SO3) in the presence of mercury salts (Hg2SO4 and HgSO4) was studied applying the density functional theory (DFT) at the UB3LYP/6-31+G(d,p) level. It was found that this reaction occurs in the free radical chain path as follows: mercury(I) sulphate free radical is generated by heat, causing CF3CCl3 to produce the CF3CCl2 free radical which reacts with SO3 leading to the formation of CF3CCl2OSO2 decomposing into CF3COCl and SO2Cl. The SO2Cl free radical triggers CF3CCl3 to regenerate CF3CCl2 which recycles the free radical growth reaction. This elementary reaction has the highest energy barrier and it is therefore the rate control step of the whole reaction path. Experiment data can confirm the existence of the mercury(I) salt free radical and the free radical initiation stage. So, mercury salts play the role of initiators not that of catalysts. The results agree well with our hypothesis.
Co-reporter:Yingjun Xu;Haifeng Zheng;Shenfeng Yuan;Zhirong Chen
Journal of Applied Polymer Science 2011 Volume 119( Issue 4) pp:2326-2333
Publication Date(Web):
DOI:10.1002/app.32928

Abstract

Amino polysiloxanes (APSs) with different amino values and amino types were synthesized and applied to cotton fabrics. Softening and smoothening properties of the fabrics treated with APSs were investigated and evaluated by measuring wrinkle recovery angles and friction coefficients, and the morphological features of the APSs adsorbed onto cellulose substrate films were characterized by atomic force microscope (AFM). The results indicate that the amino values and amino types of the APSs have a significant impact on the softening and smoothening properties of the fabrics. APSs with relatively high amino values exhibit superior smoothening property, while APSs with moderate amino values exhibit excellent softening property. Compared to the traditional softener N-β-aminoethyl-γ-aminopropyl polydimethylsiloxane (APS-1), the new amino type softeners γ-piperazinylpropyl polydimethylsiloxane (APS-2) and N-γ'-dimethylaminopropyl-γ-aminopropyl polydimethylsiloxane (APS-3) gave better fabric performance, whereas aminopropyl polydimethylsiloxane (APS-4) and N-cyclohexyl-γ-aminopropyl polydimethylsiloxane (APS-5) gave unsatisfactory fabric performance. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

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