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Combustion Synthesis and Photoluminescent Properties of Ca3((P,V)O4)2: Eu3+ Nanophosphor Xiao-jun Wang1, a and Xiao-chun Zhou2, b 1Key Laboratory of Numerical Control Technology of Guangdong Higher Education Institutes, Mechanical and Electronic Department of Guangdong Polytechnic Normal University, Guangzhou 510635, china 2School of Chemistry and Chemical Engineering, Jinggangshan University, Ji’an, Jiangxi 343009, China awxj65881010@163.com, bncdxzxc@163.com Keywords: Nanophosphors; Ca3((P,V)O4)2: Eu3+; special morphology; combustion method.
Herein, we systematically present combustion synthesis, structure characteriazation and photoluminescent properties of the Ca3((P, V)O4)2: Eu3+ nanophosphors.

Ismarrubie2c, M.Z.A.Rahman3d 1 Laboratory of Advanced Materials and Nanotechnology, Institute of Advanced Technology, 2 Department of Mechanical and Manufacturing Engineering, 3 Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia aKandhalawi_86@yahoo.com, bsapuan@eng.upm.edu.my, crubie@eng.upm.edu.my, dmzaki1212@putra.upm.edu Keywords: sugar palm tree, unsaturated polyester, bending strength, stiffness Abstract.
Kamarudin, A.Khairul : Chemical composition, morphological characteristics, and cell wall structure of Malaysia oil palm fibres.

Preparation and infrared emissivity study of optically active polyurethane/multiwalled carbon nanotubes nanocomposites Jing Chen1, a, Bingxin Liu1, b, Xiubi Chen1, c, Lixin Xue1, d, Yuming Zhou2,e 1Polymers and Composites Division, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang, 315201, China 2 College of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China achenjing@nimte.ac.cn, bliubingxin@nimte.ac.cn, cchenxiubi@nimte.ac.cn, dxuelx@nimte.ac.cn, efchem@seu.ed.u.cn Keywords: Polyurethane; Binaphthyl; Nanocomposites; Carbon nanotubes; Infrared emissivity Abstract.
During the past few years great attention has been paid to carbon nanotubes (CNTs) due to their special one-dimensional structure, extraordinary mechanical, thermal, and electrical properties.

Synthesis of Ti3AlC2 Powder by High Energy Ball Milling and High Temperature Heat Treatment Jianfeng Zhu a,*, Guoquan Qi b, Haibo Yangc and Fen Wang d Key Laboratory of Auxiliary Chemistry & Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science & Technology, Xi'an, 710021, China a zhujf@sust.edu.cn, bqgqstar@163.com, cyanghaibo@sust.edu.cn, d wangf@sust.edu.cn Keywords: Ti3AlC2; High energy milling; Reaction Mechanism; Microstructure Abstract.
Fig. 2 SEM image of unmilled powders (a); and (b) milled for 24 h However, the as milled powders have large particle size, which may be attributed to agglomeration, and some of them have layered structure (Fig.2b).

Preparation and Characterization of AlOOH/Polyimide Nanocomposite Membrane Haida Liaoa, Weiping Zhang, Xiaoming Sun, Fangfang Wang and Xinsi Lan College of Chemistry and Ecology Engineering, Guangxi University for Nationalities, Nanning 530006, China a lhd21c@tom.com Keywords: AlOOH; sol-hydrothermal crystallization; polyimide Abstract: Using metallurgical grade aluminum hydroxide as the raw material self-dispersed g-AlOOH nano-powders were made by sol-hydrothermal crystallization and the charge process.
In 1961, Bugosh [2] prepared γ-AlOOH for the first time, whose structure consisted of Al(OOH)6 octahedral layers.

Preparation of High Thermal Expansion Coefficient Glass-Ceramics in Li2O-ZnO-SiO2 System Zhuohao Xiao1,2,a, Ligang Zhu3, b and Shenglong Wang4, c 1 School of Materials Science and Engineering, Jingdezhen Ceramic Institute 333001, China 2 Jiangxi Key Laboratory of Advanced Ceramic Materials, Jingdezhen 333001, China 3 School of Chemistry and Materials Science, Yulin Normal University, Yulin 537000, China 4 National Plateau Wetlands Research Center, Southwest Forestry University, Kunming 650224, China a xiaozhuohao@126.com, b zhuligang1@163.com, c shenglongw@gmail.com Keywords: Glass-ceramics; Li2O-ZnO-SiO2; Crystallization; Thermal expansion coefficient.
The peak attributed to the thermal effect caused by the molecular rearrangement in the structure of matrix glass, which means the crystal nuclei can be formed if the glass is treated at this temperature.

SEM photo of equilibrium hydrogel Use the Scanning Electron Microscope (SEM) to investigate the inner structure of hydrogel under different pH solution.
Part A-Pure and Applied Chemistry Vol.41,(2004), P.419 [8] Sheng-Li Chen,Shuangfei Wang,Lucian A.Lucia Colloid & InterfaceSci. (2004)

Efficient Synthesis and Properties of a Photochromic Diarylethene Bearing Thiophene and Isoxazole Moieties Hongliang Liu, Gang Liu*, Shiqiang Cui, Weijun Liu Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, P.R.China liugang0926@163.com Keywords: Diarylethene; Isoxazole; Photochromism; Fluorescence; Optical storage recording.
The structure of 1o was characterized by 1H NMR spectroscopy. 1H NMR (400 MHz, CDCl3): δ 2.05 (d, 6H, J = 8.0 Hz, -CH3), 2.24 (s, 3H, -CH3), 7.29 (s, 1H, thiophene-H), 7.54 (m, 2H, benzene-H), 7.69 (d, 2H, J = 8.0 Hz, benzene-H), 7.75 (s, 1H, benzene-H).

Synthesis and Property of a Novel Diarylethene Based on Benzofuran and Thienyl Units for Polarization Optical Recording Taofeng Wang, Shouzhi Pu*, Shiqiang Cui Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, P.
The structure of 1a was characterized by 1H NMR (400 MHz, CDCl3, TMS): δ 2.29 (s, 3H, -CH3), 2.41 (s, 3H, -CH3), 6.81 (d, 1H, J = 8.0 Hz), 7.11 (d, 1H, J = 8.0 Hz), 7.35 (m, 2H), 7.87 (m, 2H): Scheme 2.

Study on Advanced Composite Synthesis of a New Photochromic Diarylethene Materials with Bearing Thiophene Units Hui Li, Yuanming Tu and Gang Liu* College of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University Nanchang 330013, P.
The structure of compound 1o was confirmed by 1H NMR. 1H NMR (400 MHz, CDCl3, TMS): δ 1.87 (s, 3H, -CH3), 1.96 (s, 3H, -CH3), 2.43 (s, 3H, -CH3), 2.48 (s, 3H, -CH3), 6.75 (s, 1H, thiophene-H), 6.97 (s, 1H, thiophene-H), 7.29-7.35 (m, 4H, benzene-H).