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Preparation and Structure of a novel PS/Fe3O4 nanochain LI YANG1,A, ZIYANG LU2,B, LILI YANG1,C, XIAOXU ZHAO1,D, ZHI ZHU1,E, NAILING GAO1,F, YOUSHAN WANG1,G, YONGSHENG YAN1,H* 1School of Chemistry & Chemical Engineering, Jiangsu University, Jiangsu, Zhenjiang 212013, PR China 2School of the Environment and Safety Engineering, Jiangsu University, Jiangsu, Zhenjiang 212013, PR China ajiangsuzj@163.com, bluziyang163@163.com, cphotocatalysis@163.com, dziyanglu@yeah.net, e117377179@qq.com, fgchxz206@126.com, gzhenjiangjs@yeah.net, hluziyang126@126.com *Corresponding author: Yongsheng Yan, e-mail address: luziyang126@126.com Keywords: Fe3O4; Nanochain; PS; Preparation; Structure Abstract The novel PS/Fe3O4 nanochain was successfully synthesized via solvothermal and self polymerization method.
These results indicated that Fe3O4 had the spherical structure, and the average diameter reached approximately 400 nm.
PS/Fe3O4 possessed good chain structure and excellent magnetic property (Ms = 37.07 emu/g).
PS/Fe3O4 possessed good chain structure.
PS/Fe3O4 possessed good chain structure and excellent magnetic property (Ms = 37.07 emu/g).

e-mail: hafizhj@ukm.my Keywords: PLZT, solid state reaction, tetragonal structure, morphological analysis, pressure sensing behaviour Abstract.
Structural investigation using XRD revealed that all samples exhibited a tetragonal crystal structure.
Numerous effort have been taken to produce PLZT ceramics such as wet chemistry methods [3,4], ball mill of oxide powders [5,6], hydrothermal process [7,8] and solid state sintering [9,10].
This result agrees with the theory which suggested that piezoelectric voltage of perovskite crystals such as PLZT occurred easier in tetragonal structure compared to pseudocubic structure.
Longe: Journal of Chemistry and Physics Vol. 103 (2007), p. 371-374 [3] A.

College of Chemistry and Chemical Engineering, Taiyuan University of Technology, No. 79 West Yingze Street, 030024,Taiyuan, Shanxi, China 2.
When the valonia extract is used to remove H2S, it is oxidized under alkaline solution firstly, which renders big tannin molecules degrade into small quinone-structured ones with oxidizing power.
In the process of desulfurization, quinone-structured compounds react with reducing materials HS- and VO2+, and are transformed to phenol-structured compounds.
[6] X.L.Zhang,H.Kang:Coordinaton Chemistry.Central South Industry University Press.Changsha. (1986),p.164
[7] X.B.Su,L.J.Dai,S.P.Chen,Y.D.Lu,Z.H.Wu: J.Chinese Chemistry and Industry of Forest Products.

The use of these materials is, however, limited by the difficulties in producing bulk materials with a nano-crystalline structure.
The aim of the work was to produce copper sintered compacts with a nanocrystalline structure using Cu powder prepared by the reduction of CuO with hydrogen.
Jose Yacaman, Materials Chemistry and Phisics, 63 (2000) 82 [8] T.S.
Świderska-Środa, 14th International Symposium on Plasma Chemistry, Symposium Proceedings, 4 (1999) 2247 [14] A.
Siemiaszko, Nanocrystalline (FeAl-TiC) 15th International Symposium on Plasma Chemistry, Symposium Proceedings, 7 (2001) 2885 [15] G.

Effect of Temperature on Preparation of Ammonium Polyphosphate Gousheng Liu1,2,a, Wenyan Chen2,b, Yuelong Liu1,c 1School of Chemistry and Chemical Engineering, Jiangxi Science and Technology Normal University, Nanchang 330013, China 2 State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China agsliu@ecust.edu.cn, bking22223@163.com, clylgyx@163.com Keywords: Crystalline form; Ammonium polyphosphate; Flame retardant; XRD.
It is reported that APP-II has strongest peak at d value of 3.40, close to 3.42 in sample 4# and 3.41 in sample 5#, it is certain that when crystalline forms transfer from one form to anohter, the long chain structure of polyphosphate in APP changs, the distance between different long chain structure of polyphosphate in APP, which is interacted by plenty of hydrogen bonds between each other, has also changed, leading to its different crystalline structure.
In this process, some inpurity peaks are coexisted in the peaks as shown in table 1, it is because the transformation from one crystalline form to other require a certain time, those products which are not fully converted from APP-II to APP-V are remained as their structures originally are, or as some certain intermediate strucutres.
Journal of Agriculture and Food Chemistry, Vol. 24,(1976), p.412
Industrial Engineering & Chemistry Research.

Nanosheets with close packed structure (111) plane of a face-centered-cubic structure are stretched along one of the two symmetry directions of the plane.
Secondly, surrounding the hole, the crystal structure is again near perfect.
Selvakannan, “New approaches to the synthesis of anisotropic, core–shell and hollow metal Nanostructures”, Journal of Materials Chemistry, 15(2005) 3161–3174
[6] Shin-ya Onoue, Junhui He,Toyoki Kunitake, “Fabrication of Gold Nanosheet and Nanowire by Oxygen Plasm Induced Fusion of Densely Arrayed Nanoparticles”, Chemistry Letters, 35(2006) 214-215
[13] MC Daniel, D Astruc, “Gold Nanoparticles: Assembly, Supramolecular Chemistry, Quantum-Size-Related Properties, and Applications toward Biology, Catalysis, and Nanotechnology”, Chem.

In laboratory experiments Thermal Analysis data were recorded and different solidification parameters were identified to characterize the inoculation effect of the carbon materials (amorphous and crystalline structure) in low sulphur (<0.025 %S) grey cast iron.
Introduction The structure (crystalline/amorphous ratio) and chemistry of re-carburizer are very important to control carbon recovery, iron quality, working environment, power/energy consumption, furnace lining life, tap-to- tap time, and alloy recovery [1].
Experimental Procedure Carbon raisers representative of the different as origins/structure and chemistry, were evaluated in laboratory conditions to assess the grey iron quality, especially for graphitizing characteristics: a) Calcined Petroleum Coke (CPC), representative of amorphous carbon material (95-98.7 %FC, 0.62.5 %S, 0.5-1.5 %Ash); b) Graphitized Petroleum Coke (GPC) as crystalline Synthetic Graphite (99-99.7 %FC, 0.06-0.3 %S, 0.1-0.7 %Ash); c) Recovered Partially Graphitized Packing Coke, as granular Petroleum Coke (GPCR) (97.4-97.9 %FC, 0.05-0.10 %S, 2.0-2.4 %Ash) or Metallurgical Coke (GMCR) (83-87 %FC, 0.19-0.34 %S, 11.5-16.7 %Ash) initially used to surround electrodes in electric graphitizing furnaces; d) Resistor Coke, as by-product from graphite manufacture, where calcined petroleum coke was covered with sand to act as an insulator for the furnace wall.
The two programs are differentiated by iron chemistry, carbon materials (type, quantity, grain size), the melt temperature and the quantity of FeSi75 addition.
A homogeneous structure is also a specific characteristic of the re-carburized cast irons with the second group of carbon materials.

Journal of Physics and Chemistry of Solids. 178. 111364
Material and Chemistry and Physics. 208. 248-257 [11] Lu, A.
Materials Chemistry and Physics. 224: 29-35
Soft chemistry routes for the preparation of Ag-CoFe2O4 nanocomposite, Ceram.
The effect of annealing on the crystalline structure of CoBi0.1Fe1.9O4 nanoparticles.

Silicon nanowires (SiNWs) are important candidate for high performance electronic and optoelectronic devices due to their unique structures, electrical and optical properties.
On the other hand, hydrogen bonded OH stretching vibration at 3320 cm-1 also found in the red dye due to ponceau 4R colourants which also has (–OH) bond in its chemical structure.
[8] Peng, K., Fang, H., Hu, J., Wu, Y., Zhu, J., Yan, Y. & Lee, S. (2006) Chemistry – A European Journal, 12, 7942-7947
P., Sivakumar, V. & Tennakone, K. (2006) Journal of Photochemistry and Photobiology A: Chemistry, 177, 324-327
[14] Jain, R., Bhargava, M. & Sharma, N. (2002) Industrial & Engineering Chemistry Research, 42, 243-247

Leskelä 1 1 Department of Chemistry, University of Helsinki, P.O.
A double layer structure of thickness approximately 100 nm PbS + 100 nm CdS was grown.
The XRD pattern of a PbS/CdS double layer structure is given in Figure 1.
The surface structure of the PbS-CdS films was analyzed by AFM.
Leskelä: Journal of Materials Chemistry, Vol. 6 (1996), p.161 6.