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Online since: January 2017
Authors: S. Paschen, Xu Dong Sun, Xin Lin Yan, Yue Dong, Zhao Hui Tang, Xue Yong Ding
The research then focused on materials in which some atoms only weakly bound to the others in the crystal structure.
This might be due to the sluggish kinetic factor of the components for such a complex crystal structure during reactions.
The increase of S with increasing temperature, even sign-changing, corresponds sensitively to the band structure of materials.
This indicates that the substitution can change significantly the electronic band structure, which is also reflected by the temperature dependent Seebeck coefficient.
Zintl's work for the modern chemistry of intermetallics, Annu.
This might be due to the sluggish kinetic factor of the components for such a complex crystal structure during reactions.
The increase of S with increasing temperature, even sign-changing, corresponds sensitively to the band structure of materials.
This indicates that the substitution can change significantly the electronic band structure, which is also reflected by the temperature dependent Seebeck coefficient.
Zintl's work for the modern chemistry of intermetallics, Annu.
Online since: March 2007
Authors: Kenichiro Ota, Shigenori Mitsushima, Nobuyuki Kamiya, Akimitsu Ishihara, Shotaro Doi, Yan Liu
The higher temperature of heat treatment caused the change of
crystalline structure and the increase of the crystallinity of ZrOxNy.
While, the crystal structure of ZrOxNy changed at around 500 oC.
Therefore, the change of temperature dependence of ORR current density was probably caused by the change of crystal structure.
This means that the crystal structure might have a large effect on the electrocatalytic activity for ORR.
[15] Landolt-Börnstein, Phase Equilibria, Crystallographic Data of Binary Alloys: Physical Chemistry (Group IV), volume 5, p.115 (1998).
While, the crystal structure of ZrOxNy changed at around 500 oC.
Therefore, the change of temperature dependence of ORR current density was probably caused by the change of crystal structure.
This means that the crystal structure might have a large effect on the electrocatalytic activity for ORR.
[15] Landolt-Börnstein, Phase Equilibria, Crystallographic Data of Binary Alloys: Physical Chemistry (Group IV), volume 5, p.115 (1998).
Online since: October 2009
Authors: Reinhard Krause-Rehberg, N.Yu. Arutyunov, Valentin V. Emtsev
This decrease is accompanied by a lessening
of intensity of the high-momentum emission of the annihilation radiation thus bringing in a direct
evidence of a multi-vacancy structure of the vacancy-group-V-impurity atom complexes after n-pconversion;
the electron density was found to be affected by the localized deep acceptor states
related to these centers.
The electron structure of the ion core of As5+ closely resembles that of Ge4+ ion core whose subvalent shells are capable of interpenetrating thus affecting the overlapping of the positron and core electrons wave functions.5 Similarity of electron structure of As5+ and Ge4+ ion cores makes for increasing of the electron density around the positron due to relaxation effects.6 Electron Density Beyond Ion Cores in DV Complexes (Materials Before n-p-Conversion).
Barbiellini, in: New Directions in Antimatter Chemistry and Physics, edited by C.M.
The electron structure of the ion core of As5+ closely resembles that of Ge4+ ion core whose subvalent shells are capable of interpenetrating thus affecting the overlapping of the positron and core electrons wave functions.5 Similarity of electron structure of As5+ and Ge4+ ion cores makes for increasing of the electron density around the positron due to relaxation effects.6 Electron Density Beyond Ion Cores in DV Complexes (Materials Before n-p-Conversion).
Barbiellini, in: New Directions in Antimatter Chemistry and Physics, edited by C.M.
Online since: April 2012
Authors: Bo Huang, Jin Sheng Zhang, Zhi Wang, Yan Jie Kong
The selected CNC equipment adopts an open structure and an oblique base.
In the consideration of the ease of mobility and the human nature of operation, the external structure of traditional CNC machine is improved from the following aspects: both the left and the right side are changed into open structure to facilitate the transmission of products on the equipment; the base adopts the oblique type, getting an angle of 53 degree from the horizontal plane; rollers are installed on the table along the two directions, so the automatic positioning and transmission of products can be realized
Beijing: Chemistry Industry Publisher, 2004, 10-22
In the consideration of the ease of mobility and the human nature of operation, the external structure of traditional CNC machine is improved from the following aspects: both the left and the right side are changed into open structure to facilitate the transmission of products on the equipment; the base adopts the oblique type, getting an angle of 53 degree from the horizontal plane; rollers are installed on the table along the two directions, so the automatic positioning and transmission of products can be realized
Beijing: Chemistry Industry Publisher, 2004, 10-22
Online since: January 2019
Authors: Zhang Hu, Ya Qi Qin, Si Tong Lu, Chu Ru Huang, Ze Kun Chen
Preparation and Properties of Chitosan-Tranexamic Acid Salts
Zhang Hua*, Yaqi Qinb, Sitong Luc, Churu Huangd and Zekun Chene
School of Chemistry and Environmental Science, Guangdong Ocean University, Zhanjiang 524088, Guangdong, China
ahuzhangqyx@126.com, b2516927675@qq.com, csmelilst@163.com, d983621355@qq.com, e2452723438@qq.com
Keywords: chitosan, tranexamic acid, salts, hemostasis
Abstract.
The physical properties including water solubility and stability of the prepared samples were tested, and their structures were characterized by Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD).
The physical properties and chemical structure of chitosan-tranexamic acid salts were determined, and the preliminary hemostatic activity was evaluated in vitro as well.
The chemical structure analysis of chitosan-tranexamic acid salts was conducted by FTIR as shown in Figure 1.
The physical properties including water solubility and stability of the prepared samples were tested, and their structures were characterized by Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD).
The physical properties and chemical structure of chitosan-tranexamic acid salts were determined, and the preliminary hemostatic activity was evaluated in vitro as well.
The chemical structure analysis of chitosan-tranexamic acid salts was conducted by FTIR as shown in Figure 1.
Online since: October 2014
Authors: Jing Kun Xu, Lu Han, Yong Luo Qiao, Wei Qiang Zhou, Liang Shen
The Electrosynthesis and Characterization of Thienyl-group-bearing Acrylic Polymer as Precursor for Electrochemical Reaction of Thiophene Side-chain
Lu Hana, Yongluo Qiao, Weiqiang Zhou, Liang Shenb*, Jingkun Xuc*
Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, P.
The structure, electrochemical, optical, thermal properties and morphology of as-formed electropolymer were systematically investigated by FT-IR, cyclic voltammetry, UV-vis, thermogravimetry and scanning electron microscopy.
With the continuous development of conducting polymers during the latest decades, the interest in settling the problem about poor processability, including poor film-forming ability, poor solubility and thermal tractability, induced by the stiff polyconjugation structure drives intensely several workers to combine the thiophene ring with a conventional insulating polymer, which can increase the solubility of the resulting block or graft copolymers[8].
In general, the lower potential is beneficial to get high-quality film while, under the high potential, it can easily result in peroxidation accompanied with side reactions, which produces conducting polymers with poor properties, even to destroy the their structures[15].
The structure, electrochemical, optical, thermal properties and morphology of as-formed electropolymer were systematically investigated by FT-IR, cyclic voltammetry, UV-vis, thermogravimetry and scanning electron microscopy.
With the continuous development of conducting polymers during the latest decades, the interest in settling the problem about poor processability, including poor film-forming ability, poor solubility and thermal tractability, induced by the stiff polyconjugation structure drives intensely several workers to combine the thiophene ring with a conventional insulating polymer, which can increase the solubility of the resulting block or graft copolymers[8].
In general, the lower potential is beneficial to get high-quality film while, under the high potential, it can easily result in peroxidation accompanied with side reactions, which produces conducting polymers with poor properties, even to destroy the their structures[15].
Online since: November 2023
Authors: Haryani Haryani, Takeshi Kato, Daiki Oshima, Nurul Imani Istiqomah, Edi Suharyadi
X-Ray diffraction spectra showed that the crystal structure of NiZnFe2O4/SiO2 has a mixed cubic spinel structure.
Results and Discussion Crystal Structure Figure 3.
XRD shows that the crystal structure of NiZnFe2O4/SiO2 is a mixed cubic spinel structure, due to NiFe2O4 with inverse spinel structure and ZnFe2O4 a normal spinel structure.
NiZnFe2O4/SiO2 has a mixed cubic crystal structure, with the highest particle size of 9.6 nm.
Chen, “Multifunctional Mesoporous Silica Nanoprobes: Material Chemistry–Based Fabrication and Bio-Imaging Functionality,” Adv.
Results and Discussion Crystal Structure Figure 3.
XRD shows that the crystal structure of NiZnFe2O4/SiO2 is a mixed cubic spinel structure, due to NiFe2O4 with inverse spinel structure and ZnFe2O4 a normal spinel structure.
NiZnFe2O4/SiO2 has a mixed cubic crystal structure, with the highest particle size of 9.6 nm.
Chen, “Multifunctional Mesoporous Silica Nanoprobes: Material Chemistry–Based Fabrication and Bio-Imaging Functionality,” Adv.
Online since: January 2015
Authors: K.A. Koparkar, N.S. Bajaj, S.K. Omanwar
More over controlled synthesis method conditions may apply on it to have structure like carbon nanotubes used for various modern applications.
El-Sayed, Chemistry and properties of nanocrystals of different shapes, Chem.
Chi, Mechanochromic Fluorescent Materials: Phenomena, Materials and applications, Royal Society of Chemistry, UK, 2014
Royal Society of Chemistry, London, 1988
Muenchausen, Y2O3:Bi nanophosphor: Solution combustion synthesis, structure, and luminescence, J.
El-Sayed, Chemistry and properties of nanocrystals of different shapes, Chem.
Chi, Mechanochromic Fluorescent Materials: Phenomena, Materials and applications, Royal Society of Chemistry, UK, 2014
Royal Society of Chemistry, London, 1988
Muenchausen, Y2O3:Bi nanophosphor: Solution combustion synthesis, structure, and luminescence, J.
Online since: June 2012
Authors: Li Li Wang, Xiu Feng Wang, Cheng Long Yu, Hong Tao Jiang
Crystallization Characteristics and Thermal Stability of Fluor-hydroxyapatite Composites with Zirconia
Li-li Wang1, Xiu-feng Wang, Cheng-long Yu , Hong-tao Jiang
1.Key Laboratory of Auxiliary Chemistry & Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science & Technology, Xi’an, Shaanxi, People’s Republic of China 710021, wanglili@sust.edu.cn
Keywords: Fluor-hydroxyapatite ;Zirconia ;Crystallization characteristics; Stability of sintering
Abstract.
Alternative methods to fabricate dense HA-ZrO2 composites should be introduced by changing the structure of HA, intrinsically.
Alternative methods to fabricate dense HA-ZrO2 composites should be introduced by changing the structure of HA, intrinsically.
Online since: July 2007
Authors: Katalin Gruiz, E. Vaszita, Z. Siki
Calculation of PEC from measured concentrations and the comparison of this value to the usespecific
quality criteria is a good solution for surface waters or subsurface water-bases, but the solid
phase containing environmental elements, the soil and sediment, are more complicate structures,
than the water.
Chemistry Vol. 58 (1997) p. 223 [7] K.
Chemistry Vol. 58 (1997) p. 223 [7] K.