ShangJin He

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Name: 何尚锦; ShangJin He
Organization: Nankai Univerisity , China
Department: The Key Laboratory of Functional Polymer Materials of the Ministry of Education, Department of Chemistry
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Yang Zhang;Juan Zhao;Pan Yang;Hengjian Huang
Polymer Engineering & Science 2012 Volume 52( Issue 4) pp:768-773
Publication Date(Web):
DOI:10.1002/pen.22140

Abstract

Energetic block copolymer of polyglycidylazide-b-poly (azidoethyl methacrylate) (GAP-b-PAEMA) was synthesized and characterized. Macroinitiator PECH-Br prepared via the reaction of 2-bromoisobutyryl bromide with hydroxyl-terminated polyepichlorohydrin (PECH-OH) was used to initiate the atom transfer radical polymerization (ATRP) of chloroethyl methacrylate (CEMA). After azidation of the resulting copolymer, energetic copolymer GAP-b-PAEMA was obtained. Increase in the molecular weight determined by gel permeation chromatograph (GPC) is in agreement with the formation of block copolymer. Fourier transform infrared spectroscopy (FTIR) shows that the chlorine groups in the block copolymer can be substituted by azide group easily. Thermogravimetric analysis (TGA) shows that degradation of GAP-b-PAEMA involves two steps: the instantaneous decomposition of the azide groups followed by progressive scission of the polymer backbone. From differential scanning calorimetry (DSC) analysis, the GAP-b-PAEMA copolymer exhibits two glass transition temperatures (Tg) at −18 and 36°C, suggesting that the synthesized copolymer is a thermoplastic elastomer. This research provides a new method for the synthesis of energetic polymer. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers

Co-reporter:Shang-Jin He, Yang Zhang, Zhen-Hua Cui, Yuan-Zhi Tao, Bao-Long Zhang
European Polymer Journal 2009 Volume 45(Issue 8) pp:2395-2401
Publication Date(Web):August 2009
DOI:10.1016/j.eurpolymj.2009.04.030
Reversible addition fragmentation chain transfer (RAFT) polymerization of cholesteryl acrylate (ChA) was conducted using S-1-dodecyl-S′-(α,α′-dimethyl-α′′-acetic acid)trithiocarbonate as CTA and AIBN as initiator in toluene at 80 °C. The polymerization was investigated at two different CTA concentrations (0.025 and 0.040 M). Polymerization of ChA with CTA concentration of 0.040 M proceeds in a controlled/living manner as evidenced by linear increase of the molecular weight with conversion and narrow polymer polydispersity (PDI < 1.2). With lower initial CTA concentration, namely 0.025 M, although poly(cholesteryl acrylate) (PChA) exhibiting narrow molecular weight distributions could be synthesized, the polymerization showed relatively low control with many termination products. Chain extension polymerizations were performed starting from either the PChA or the polystyrene (PS) block, and well-defined copolymers based on ChA and styrene were prepared. Thermal properties of PChA and PS-b-PChA copolymer were investigated by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), and the results showed that both PChA and PS-b-PChA are amorphous polymers. PChA begins to decompose at ca. 218 °C with maximum weight loss rate at 351 °C, while PS-b-PChA shows double weight loss rate peaks located at 345 and 415 °C, respectively.
Co-reporter:S. J. He;K. Y. Shi;X. Z. Guo;Z. J. Du ;B. L. Zhang
Polymers for Advanced Technologies 2009 Volume 20( Issue 2) pp:130-134
Publication Date(Web):
DOI:10.1002/pat.1286

Abstract

Methylimidazole-terminated chain-extended urea (MITU) containing polypropylene oxide spacer was synthesized and employed to modify epoxies composed of a diglycidyl ether of bisphenol-A (E-51) and methyltetrahydrophthalic anhydride (MTHPA). The curing behavior, viscoelastic property, impact response, and fracture surface morphology of the curing systems were systematically investigated. Differential scanning calorimeter (DSC) analysis reveals that the curing reactivity of the epoxy system is greatly enhanced with the addition of MITU. From the dynamic mechanical analysis, besides the low-temperature β relaxation, shoulder at higher temperature side appears for the MITU-modified systems. Meanwhile, the addition of MITU leads to the increase of loss factor (tan δ) over the temperature range of 0–75°C. Impact tests show that the modifier can be effective in toughening the epoxy resin at relatively low loading, and the scanning electron microscope (SEM) images of the fracture surface for the modified systems display signs of ductility. Copyright © 2008 John Wiley & Sons, Ltd.

POLY(N,N-DIMETHYL ACRYLAMIDE)
Benzoic acid, 4-[(1E)-2-[4-[(6-azidohexyl)oxy]phenyl]diazenyl]-, 6-azidohexyl ester
Benzoic acid, 4-[(1E)-2-[4-[(6-chlorohexyl)oxy]phenyl]diazenyl]-, 6-chlorohexyl ester
1,1'-Biphenyl, 4,4'-bis[[6-(2-propyn-1-yloxy)hexyl]oxy]-
(E)-4-((4-hydroxyphenyl)diazenyl)benzoic acid
1-Hexanol, 6-chloro-, 1-(4-methylbenzenesulfonate)