Papers by Author: Ya Juan Xu

Abstract: The precursor of Co₃O₄ nanometer particles is synthesized through settles under given conditions. The decomposition process of the precipitate is studies by TGA and XRD. The results indicate that the precipitate is amorphous. With the temperature increasing the precursor firstly loses its free water and structure water. Then the precursor decomposes into Co₃O₄ nanometer particles at 321°C and change into CoO nanometer particles at 920°C.As the firing temperature and time increasing, the crystal transformation tends perfectly.

Abstract: In this paper, a system polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) were synthesized by nitroxide-medium controllable free radical polymerization. PS-b-P4VP were characterized by 1H-nuclear magnetic resonance (1H-NMR), infrared spectrum (FTIR) and gel permeation chromatography (GPC). The results have indicated that diblock copolymers can be prepared and with molecular polydispersities in the range of 1.08 to 1.31. The structure of diblock was showed by 1H-nuclear magnetic resonance.

Abstract: a system of polystyrene and polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) were synthesized by using living free radical in the presence of 4-hydroxyl-2, 2, 6, 6-tetramethylpiperridine-oxyl-1(HTEMPO•) and (BPO). The polystyrene and diblock copolymers were characterized by gel permeation chromatography (GPC) and atomic force microscope (AFM). The results suggested that the polymerization of styrene in the presence of 4-hydroxyl-2, 2, 6, 6-tetramethylpiperridine-oxyl-1(HTEMPO•) and benzoyl peroxide (BPO) can be prepared with molecular weight distribution in the range of 1.15 to 1.25. The polystyrene with living groups can continuously initiate the living free radical polymerization of 4-Vinylpyridine to form the polystyrene-block-poly (4-vinylpyridine) with molecular weight distribution in the range of 1.08 to 1.35. The AFM of diblock indicated the diblock copolymer（PS-b-P4VP） is a good compatibilizer for PS and P4VP.

Abstract: A series of blends have been prepared by adding a novel thermoplastic Poly (aryl ether) s containing phthalazinone moiety (PPAEs) in varying proportions to diglycidyl ether of bisphenol A epoxy resin (DGEBA) cured with p-diaminodiphenylsulfone (DDS). The glass transition temperature (Tg) of DGEBA /PPAEs blends were performed using differential scanning calorimetry (DSC) technique. It is proved that the addition of PPAEs resulted in enhancement of thermal properties of the blends, especially PPENK. There was moderate increase in the fracture toughness as estimated by notched impact strength. Compared to that of unmodified epoxy, the maximum toughness of the modified blends had increased 44% by addition of 15 phr PPENK. Fracture mechanisms such as plastic deformation and the ductile nature of the crack of the matrix were responsible for the increase in the fracture toughness of the blends.

Abstract: A series of blends have been prepared by adding a novel thermoplastic poly (phthalazinone ether sulfone ketone) (PPESK) in varying proportions to diglycidyl ether of bisphenol A epoxy resin (DGEBA) cured with p-diaminodiphenylsulfone. The kinetics of curing reaction and glass transition temperature (Tg) of PPESK/DGEBA blends were performed using differential scanning calorimetry (DSC) technique. It is proved that the addition of PPESK accelerated curing reaction and resulted in great enhancement of thermal properties of the blends. There was moderate increase in the fracture toughness as estimated by the critical stress intensity factor (KIc). Compared to that of unmodified epoxy, the maximum toughness of the modified blends had increased 32% by addition of 15 phr PPESK. Fracture mechanisms such as crack deflection and branches, ductile microcracks, ductile tearing of the thermoplastic of the matrix were responsible for the increase in the fracture toughness of the blends