Journal articles on the topic 'Oxidization'

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1

Mergia, K., Volker Liedtke, T. Speliotis, G. Apostolopoulos, and S. Messoloras. "Thermo-Mechanical Behaviour of HfO2 Coatings for Aerospace Applications." Advanced Materials Research 59 (December 2008): 87–91. http://dx.doi.org/10.4028/www.scientific.net/amr.59.87.

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The use of ceramic composite materials in aerospace applications requires the development of oxidization protection coatings which can withstand very high temperatures. HfO2 is a promising material as a high temperature oxidization protective layer. HfO2 coatings have been deposited by radiation frequency magnetron sputtering all over the surface of SiC substrates and were tested under re-entry conditions. Also their oxidization resistance in air in the temperature range 1100 to 1450°C has been examined. The coatings were found to be stable and well-adhering to the substrate even after 100 re-entry cycles. No oxidization of the underlying SiC structure is observed. Re-entry and oxidization tests result in the formation of HfSiO4 at the HfO2/SiC interface, which further promotes their oxidization resistance.
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2

Fu, Ying, Yan Zheng Wang, Juan Tan, Hong Lan Li, and Xin Yu Zhang. "Oxidation Behavior of Stable-Oxidative-Poly-Si-Fe (SOPSF) Coagulant." Applied Mechanics and Materials 341-342 (July 2013): 266–69. http://dx.doi.org/10.4028/www.scientific.net/amm.341-342.266.

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The oxidation behavior of a stable-oxidative-poly-Si-Fe (SOPSF) coagulant prepared by water glass and H2SO4 solution in treating a synthetic humic acid (HA) water was probed, in compraison with that of poly-Si-Fe (PSF) and Polyferric aluminum (PFA). The results revealed that the oxidization of SOPSF and PSF was very stable during the whole coagulation process, and played a role during the whole process including quiescent settling stage. While PFA almost gave no oxidization even at higher dose of 0.322 mmol.L-1. The oxidization rate of SOPSF was slower than that of SOPSF hydrolysis and destabilization process. Coagulation mechanism of SOPSF in removing dissolved organic matters (DOMs) may be a comprehensive results between the alternating interaction of oxidization/adsorption-destabilization/oxidization, bridging and sweeping.
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3

Han, Shi Zhong, Qiang Zhang, and Zhi Qiong Chen. "Non-Thermal Plasma and Catalyst System for Simultaneously Oxidizing SO2 and NOx." Advanced Materials Research 634-638 (January 2013): 864–68. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.864.

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For the requirements of nitric oxide (NOx) and sulfur dioxide (SO2) removal process in coal-fired power plant, a new non-thermal plasma system combined with catalyst was developed to investigate the effect of parameters such as temperature, atmosphere, residence time, and additives (NH3 and methanol) on NOx and SO2 conversion rate. The results indicated that the new system could greatly promote the NOx conversion rate while it only had a slight influence on the SO2 oxidization rate. Meanwhile, high temperature suppressed the NO oxidization, and promoted the SO2 oxidation. The long residence time was beneficial to the NOx and SO2 oxidization. In the absence of water, the additive of NH3 can improve NO, NOx, and SO2 oxidization rate due to the reactions between NH3 and NOx, or SO2. Contrary to NH3, methonal had a negative effect on NOx and SO2 oxidization.
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4

Miroshnichenko, D. V., and Yu S. Kaftan. "The oxidization of coal." Coke and Chemistry 60, no. 5 (May 2017): 177–84. http://dx.doi.org/10.3103/s1068364x17050052.

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5

Zou, Xing. "Improving in Oxidization Kinetics of Manganese Sulfate Hydrolyzates in Alkaline Solution Media." Advanced Materials Research 538-541 (June 2012): 2448–52. http://dx.doi.org/10.4028/www.scientific.net/amr.538-541.2448.

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The oxidization of hydrolyzates of manganese sulfate had been investigated in ammoniacal solution. The results show that hydrolyzates of manganese sulfate are oxidized slowly by air, furthermore, their oxidization rate less depends on temperature and acidity in the ranges of their respective certain values, but the oxidization rate for hydrolyzates of manganese sulfate can be increased significantly by adding some additives, activatiing hydrolyzates or changing molecular structure of hydrolyzates.
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6

Wang, Li Ping, Wei Juan Jiang, Er Deng Du, Chu Qiao Wang, and Nai Yun Gao. "Treatment of Lake-Type Raw Water by Ultrasonic and Photocatalytic Oxidization Process." Advanced Materials Research 156-157 (October 2010): 127–31. http://dx.doi.org/10.4028/www.scientific.net/amr.156-157.127.

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The lake-type raw water was treated in a photocatalytic oxidization reactor. The experiment was carried out using ultrasonic under the condition of flow rate 10L/h, the padding packing compares 2/5, UV lamp 30W, non-additional chemicals, pH 7.35. Moremore, the raw water also was treated by ultrasonic / photocatalytic oxidization integrated process under the same control conditions. The results indicate that, after ultrasonic / photocatalytic oxidization process for 36 hours, the average removal of CODMn, TP, Chl-a and OD560 were 25.3%, 30.1%, 98.6% and 88.1%, respectively.
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7

Eliezer, Amir. "Corrosion Behavior of Surfaced AM50 Magnesium Alloys under Stress Conditions." Advanced Materials Research 95 (January 2010): 79–83. http://dx.doi.org/10.4028/www.scientific.net/amr.95.79.

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Micro-arc oxidization of AM50 magnesium alloys was studied. The influence of micro-arc oxidization process was investigated; phase structure were analyzed using X-ray diffraction (XRD). Open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) were used to evaluate the corrosion resistance of ceramic coatings formed on magnesium alloys under stress conditions. XRD analyses indicate that the ceramic coatings fabricated on the surface of magnesium alloys by micro-arc oxidization are composed of spinel phase MgAl2O4 The corrosion resistance of ceramic coatings is improved compared with magnesium alloy substrate.
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8

Xu, Shu Qiong. "Research of New Type PAN-Based Carbon Fiber Pre-Oxidization Furnace and its Temperature Controlling Property." Advanced Materials Research 189-193 (February 2011): 1969–72. http://dx.doi.org/10.4028/www.scientific.net/amr.189-193.1969.

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A new type pre-oxidization furnace used for producing PAN-based carbon fiber has been developed. Practical operations showed that the furnace possesses characteristics of reasoanable design, higher temperature controlling precision and high hot efficiency. It is an ideal pre-oxidization furnace.
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9

Nanjo, Junji, and Shigeru Nomura. "Surface oxidization of semiconducting silicon." Bulletin of the Japan Institute of Metals 24, no. 9 (1985): 739–45. http://dx.doi.org/10.2320/materia1962.24.739.

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10

Zhang, Yu Wei, Jin Yong Zhang, Jing Jing Xie, and Zheng Yi Fu. "ZrC Oxidization Mechanism in Air." Key Engineering Materials 512-515 (June 2012): 1721–24. http://dx.doi.org/10.4028/www.scientific.net/kem.512-515.1721.

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The ZrC oxidization mechanism in air was carefully investigated by the phase composition and grain morphology through DSC, X-ray diffraction and SEM respectively at different temperature. It was found that the oxidization of ZrC start at about 400°C by oxygen atom entering the interstitial sites to substitute part of Carbon. Zr2O and ZrO2can be formed at a temperature of about 600°C and 1000°Crespectively. And ZrC will completely transfer to ZrO2at 1000°C for 5hrs. No obvious grain morphology change was found under 600°C.
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11

Yao, Shuiliang, Chieko Mine, Satoshi Kodama, Shin Yamamoto, and Yuichi Fujioka. "Experimental Investigation of Carbon Oxidization." Chemistry Letters 38, no. 2 (February 5, 2009): 168–69. http://dx.doi.org/10.1246/cl.2009.168.

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12

Wang, Lu Cai, Jin Qiang Ai, Yan Li Wang, and Xiao Hong You. "Influences of Processing Factors on Pore Structure of Aluminum Foams." Advanced Materials Research 557-559 (July 2012): 8–12. http://dx.doi.org/10.4028/www.scientific.net/amr.557-559.8.

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Orthogonal experiments were employed to confirm the interactive effect of the addition of magnesium powder, milling time of aluminum powder, oxidization time of TiH2 on the pore structure of Aluminum foam, which prepared by PCM method. The results show that the three factors arragned in important order as the follows: oxidization time, milling time, and the quantity of magnesium powder. The high quality aluminum foam samples, with average porosity of 84.2%, average equivalent circle diameter of 1.9 mm and average circularity of 0.754, was made on the condition of milling time as 85 minutes, oxidization time as 10 minutes and magnesium powder content as 0.5 wt%.
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13

KATAHIRA, KAZUTOSHI, HITOSHI OHMORI, MASAYOSHI MIZUTANI, and JUN KOMOTORI. "INVESTIGATION ON HIGH-TEMPERATURE OXIDIZATION OF MIRROR-QUALITY GROUND STAINLESS STEEL." International Journal of Modern Physics B 24, no. 15n16 (June 30, 2010): 3005–10. http://dx.doi.org/10.1142/s0217979210065994.

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To investigate the possibility of developing a new surface modification method by the combined process of ELID grinding and high-temperature oxidization, we treated ELID finished specimens and polished specimens by high-temperature oxidization in the atmosphere and performed detailed analysis to determine how the treatment would change the specimen surfaces. The ELID-series showed high quality surface roughness and excellent tribological characteristics as compared with the polished-series. The improved surface properties of the ELID-series seem to result from formation of fine, uniform structures of spinel-type multiple oxides FeCr 2 O 4 and Cr 2 O 3 on the surface by high-temperature oxidization.
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14

Ding, Xin Geng, and Li Li. "The Physical and Antibacterial Properties of Argentine-Doped TiO2 Film on Stainless Steel Substrate." Key Engineering Materials 280-283 (February 2007): 801–4. http://dx.doi.org/10.4028/www.scientific.net/kem.280-283.801.

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The aim of the present study is to investigate the physical properties and antibacterial performances of Ag+-doped TiO2 film on stainless steel and effects of surface oxidization. In the experiment, the surface of stainless steel was been oxidized by heat treatment (550°C, 1 hour) before the Ag+-doped TiO2 (anatase) film being formed by sol-gel method. Sample A (filmed after surface oxidization), B (filmed without surface oxidization), C (only surface oxidization) and D (neither oxidized nor filmed) were respectively tested for corrosive resistance, abrasive resistance and adhesiveness, and the samples with different content of argentine was tested for antibacterial performance. Results: 1) Corrosion rates of sample A, B, C and D in 10% FeCl3 solution are respectively 1.65%, 1.87%, 2.02% and 3.28%, suggesting that the film has protected the stainless steel from the corrosion; 2) Scratching using a loaded (150 g) pin makes no crack on surface of sample A, while it results a slight scuffing on surface of sample B, suggesting that the surface oxidization has enhanced the abrasive resistance and adhesiveness of the TiO2 film, which may be due to the bridge-like function of the oxidation film; 3)Antibacterial performance is enhanced as the content of doping argentine increases, exceeding 90% when the argentine reached 3%, and the TiO2 film on the oxidized stainless steel performs better in antibacterial test than untreated one.
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15

Pilban Jahromi, Siamak, Nay Ming Huang, Ahmad Kamalianfar, Hong Ngee Lim, Muhamad Rasat Muhamad, and Ramin Yousefi. "Facile Synthesis of Porous-Structured Nickel Oxide Thin Film by Pulsed Laser Deposition." Journal of Nanomaterials 2012 (2012): 1–4. http://dx.doi.org/10.1155/2012/173825.

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Porous-structured nickel oxide (PsNiO) was obtained through the oxidization of a nickel thin film. The nickel thin film was deposited using the pulsed laser deposition (PLD) method on a nickel foil as a substrate. The results show uniform PsNiO after the oxidization of the nickel thin film at 750∘C for 1 h. X-ray diffraction (XRD) indicates formation of the NiO crystalline structure. Field emission scanning electron microscopy (FESEM) reveals different morphology on the surface of the nickel foil (sample A) and on the nickel thin film (sample B). Comparison of the FESEM results after oxidization shows that the PsNiO on the nickel thin film was more regular and controllable than the NiO layer on the nickel foil. The FESEM images also show that the thickness of the nickel thin film affected the PsNiO size obtained after oxidization. This resulted from the growth of the porous structure at grain boundaries and from the grain sizes. The electrochemical properties of the PsNiO as an electrode are investigated by cyclic voltammetry (CV). These results show the effect of PsNiO size on the current of anodic peak.
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16

Ganster, Patrick, Guy Tréglia, Frédéric Lancon, and Pascal Pochet. "Molecular dynamics simulation of silicon oxidization." Thin Solid Films 518, no. 9 (February 2010): 2422–26. http://dx.doi.org/10.1016/j.tsf.2009.09.144.

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17

Hongbo, Tang, Li Yanping, Zhang Wen, and Dong Siqing. "Synthesis, Optimization, Property, Characterization, and Application of Dialdehyde Cross-Linking Guar Gum." International Journal of Polymer Science 2016 (2016): 1–14. http://dx.doi.org/10.1155/2016/6482461.

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Dialdehyde cross-linking guar gum (DCLGG), as a novel material, was synthesized using phosphorus oxychloride as a cross-linking reagent, sodium periodate as an oxidant, and ethanol as a solvent through keeping the original particle form of guar gum. The process parameters such as the reaction temperature, reaction time, pH, amount of sodium periodate, and amount of ethanol were optimized by the response surface methodology in order to obtain the regression model of the oxidization. The covalent binding of L-asparagine onto the surfaces of DCLGG was further investigated. The results showed that the best technological conditions for preparing DCLGG were as follows: reaction temperature = 40°C, reaction time = 3.0 h, pH = 4.0, and amount of ethanol = 74.5%. The swelling power of DCLGG was intermediate between cross-linking guar gum and dialdehyde guar gum. The cross-linking and dialdehyde oxidization reduced the viscosity of GG. The cross-liking reduced the melting enthalpy of GG. However, the oxidization increased melting enthalpy of ACLGG. The thermal stability of GG was increased by cross-linking or oxidization. The variation of the onset decomposition temperature and end decomposition temperature of GG was not consistent with thermal stability of GG. L-asparagine could be chemically bound well by DCLGG through forming Schiff base under the weak acidity. The maximum adsorption capacity of L-asparagine on DCLGG with aldehyde content of 56.2% reached 21.9 mg/g.
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18

Chen, Zhi Gang, Rui Xue Zhang, Bo Zhang, and An Ping Wei. "Treatment of Sodium Formate Wastewater by Fenton Oxidation Process." Advanced Materials Research 573-574 (October 2012): 627–30. http://dx.doi.org/10.4028/www.scientific.net/amr.573-574.627.

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In this study, in order to reduce the sodium formate concentration thereby reducing toxicity, the treatment of this wastewater by Fenton process was investigated. The effects of initial PH value, reaction time, concentration of FeSO4• 7H2O, and H2O2 dosage on the removal efficiency of COD were studied respectively. The experiment results show that when using Fenton oxidization pretreatment process, with pH 2.0, FeSO4•7H2O concentration 4000mg/L, H2O2(30 % ) portion 4ml/L, and reaction time 20min, COD removal efficiency was more than 50%, oxidization efficiency was good.
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19

Zhou, Su-Qin, Yang-Yang Wu, Si-Yu Xu, Feng-Qi Zhao, and Xue-Hai Ju. "Oxygen adsorption and diffusion on an Al(111) surface and subsurface: a theoretical study." Canadian Journal of Chemistry 94, no. 6 (June 2016): 541–46. http://dx.doi.org/10.1139/cjc-2015-0278.

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The generalized gradient approximation of the density functional theory was used to investigate the adsorption and dissociation of the O2 molecule on an Al(111) surface and the subsequent diffusion of an oxygen atom into the subsurface with different oxygen coverages. The total adsorption energies of oxygen atoms on the Al(111) surface increase as the number of adsorbed oxygen atoms increases, while the adsorption heats per oxygen atom decrease firstly and then increase. The adsorption heats for O2 physisorption on the Al(111) surface would increase as the oxidization degree of Al(111) surface increased. As the oxidization degree of Al(111) surface increases, the adsorption heats for O2 chemisorption decrease firstly and then increase, and the O2 molecule would not dissociate when the oxidization degree was up to 1.0 monolayer. In general, the energy barriers for both the interlayer and intralayer diffusions of the oxygen atom on the Al(111) surface would become larger as the number of initial adsorbed oxygen atoms on the Al(111) surface increased due to an increasing repulsion force.
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20

Yang, Chi, Baoxiang Gu, Dan Zhang, Cunwang Ge, and Huimin Tao. "Coaxial carbon fiber/ZnO nanorods as electrodes for the electrochemical determination of dopamine." Analytical Methods 8, no. 3 (2016): 650–55. http://dx.doi.org/10.1039/c5ay02928g.

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21

Huang, Yi Hong, Jian Hua Chen, Li Jing Ling, Zhen Bo Su, Xue Sun, Shi Rong Hu, Wen Weng, Yang Huang, Wen Bing Wu, and Ya San He. "Simultaneous electrochemical detection of catechol and hydroquinone based on gold nanoparticles@carbon nanocages modified electrode." Analyst 140, no. 23 (2015): 7939–47. http://dx.doi.org/10.1039/c5an01738f.

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22

Cheng, Jin, Xiao Ping Zou, Xiang Min Meng, Gang Qiang Yang, Xue Ming Lü, Cui Liu Wei, Zhe Sun, Hong Ying Feng, and Yuan Yang. "Electrochemical Deposition of Metallic Lead Particle Film." Advanced Materials Research 123-125 (August 2010): 423–26. http://dx.doi.org/10.4028/www.scientific.net/amr.123-125.423.

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The preparation of metallic lead films by electrochemical deposition was reported. Although primary deposits at fresh state (also referred to as fresh deposits) were indeed metallic lead films, the fresh lead films could be rapidly oxidized to lead oxide in air. To obtain long stable metallic lead films, the key process is how to prevent the oxidization of fresh lead films. Our studies indicate that the washing of fresh metallic lead films in absolute alcohol is a simple but effective method to protect the lead films from the oxidization for an extended period of more than 20 days.
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23

Xue, Duomei, Zeren Chen, Jiayuan Liu, Jingyao Liu, Di Wu, Ying Li, and Zhiru Li. "Oxidization of aromatic heterocyclic molecules with superhalogens." Polyhedron 201 (June 2021): 115160. http://dx.doi.org/10.1016/j.poly.2021.115160.

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24

Vyrina, E. E., O. N. Lukatcheva, N. A. Voinov, and Yu D. Alashkevitch. "Intensification of Water Oxidization in the Aerotank." Ecology and Industry of Russia 19, no. 11 (November 11, 2015): 10. http://dx.doi.org/10.18412/1816-0395-2015-11-10-12.

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25

Yasuma, Airi, Ayaka Yamanaka, and Susumu Okada. "Energetics of edge oxidization of graphene nanoribbons." Japanese Journal of Applied Physics 57, no. 6S1 (May 8, 2018): 06HB03. http://dx.doi.org/10.7567/jjap.57.06hb03.

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26

Sakurai, Hirohisa, and Osamu Tamura. "Oxidization Characteristics of Standard Platinum Resistance Thermometers." Japanese Journal of Applied Physics 50, no. 3R (March 1, 2011): 036601. http://dx.doi.org/10.7567/jjap.50.036601.

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27

Sun, Jinxu, Huixia Zhu, and Guangxiao Dong. "Oxidization Resistance in Vivo for Raspberry Flavone." Engineering 05, no. 10 (2013): 455–58. http://dx.doi.org/10.4236/eng.2013.510b093.

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28

OTANI, KOICHI. "Neuroplegics malignant syndrome and genetic drug oxidization." Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics 23, no. 1 (1992): 183–84. http://dx.doi.org/10.3999/jscpt.23.183.

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29

Sakurai, Hirohisa, and Osamu Tamura. "Oxidization Characteristics of Standard Platinum Resistance Thermometers." Japanese Journal of Applied Physics 50 (March 22, 2011): 036601. http://dx.doi.org/10.1143/jjap.50.036601.

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30

Tanaka, Masahiro, and Miho Ami. "Kinetics of Oxidization Processes of Ruthenium Particles." Journal of the American Ceramic Society 81, no. 10 (January 21, 2005): 2513–16. http://dx.doi.org/10.1111/j.1151-2916.1998.tb02655.x.

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31

Shen, Wenzhong, Hui Wang, Yihong Liu, Qingjie Guo, and Yuanli Zhang. "Oxidization activated carbon fiber through nitrocellulose combustion." Colloids and Surfaces A: Physicochemical and Engineering Aspects 308, no. 1-3 (October 2007): 20–24. http://dx.doi.org/10.1016/j.colsurfa.2007.05.023.

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32

Zhu, Xian, and Qian Wang. "Toluene oxidization to benzaldehyde in subcritical water." Journal of Shanghai University (English Edition) 10, no. 1 (February 2006): 86–88. http://dx.doi.org/10.1007/s11741-006-0110-x.

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33

Tarraf, M., M. Soltan, and A. Elweteedy. "Gas Phase Air Cleaning Using Catalytic Oxidization." International Conference on Aerospace Sciences and Aviation Technology 15, AEROSPACE SCIENCES (May 1, 2013): 1–12. http://dx.doi.org/10.21608/asat.2013.22271.

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34

Yang, M., J. Hu, and K. Ito. "Characteristics of Fe2+/H2O2/UV Oxidization Process." Environmental Technology 19, no. 2 (February 1998): 183–91. http://dx.doi.org/10.1080/09593330.1998.9618629.

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35

Zhang, Yuanjian, and Dongfeng Xue. "Oxidization Route and Pseudocapacitance of Manganese Oxides." Materials Focus 1, no. 2 (August 1, 2012): 154–59. http://dx.doi.org/10.1166/mat.2012.1024.

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Wang, Yanqing, Yuemeng Li, Liping Ding, Yanfeng Tang, and Jun Ding. "Low-cost valence-rich copper–iron–sulfur–oxygen porous nanocluster that drives an exceptional energy-saving carbohydrazide oxidization reaction in alkali and near-neutral electrolytes." Journal of Materials Chemistry A 8, no. 46 (2020): 24419–27. http://dx.doi.org/10.1039/d0ta09295a.

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37

Zhao, Jianfeng, Ruixue Zhu, Xiting Zhang, Bowu Zhang, Yancheng Liu, Yuanchun Li, Wenfeng Wang, and David Lee Phillips. "A photoenhanced oxidation of amino acids and the cross-linking of lysozyme mediated by tetrazolium salts." Physical Chemistry Chemical Physics 23, no. 6 (2021): 3761–70. http://dx.doi.org/10.1039/d0cp04887a.

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38

Ivashchuk, Oleksandr, and Victor Reutskyy. "Research of action mechanism of catalytic solutions in the oxidization process of cyclohexane." Chemistry & Chemical Technology 2, no. 2 (June 15, 2008): 85–90. http://dx.doi.org/10.23939/chcht02.02.085.

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In the article intercommunication is considered between efficiency of action of difficult catalytic solutions [cobalt naftenate – polyethyleneglicol – cyclohexanone] in the process of liquid-phase oxidization of cyclohexane and complexes formation between the component components of catalytic solutions.
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39

DU, XIAOFENG, NANA MA, SHILING SUN, GUOCHUN YANG, and YONGQING QIU. "THEORETICAL INVESTIGATION ON SECOND-ORDER NONLINEAR OPTICAL PROPERTIES AND REDOX-SWITCHING OF PHENYL NITRONYL-NITROXIDE RADICAL DERIVATIVES." Journal of Theoretical and Computational Chemistry 11, no. 05 (October 2012): 1075–88. http://dx.doi.org/10.1142/s021963361250071x.

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The static second-order nonlinear optical (NLO) properties on a series of phenyl nitronyl-nitroxide (NN) radical derivatives were investigated using density functional theory (DFT). It is found that the first hyperpolarizabilities of these systems are sensitive to the substituents, and system 4a containing of a two-dimensional (2D) substituent possesses the largest βtot value of 83.134 × 10-30 esu. Meanwhile, the time-dependent (TD)-PBE1PBE calculations indicate that low transition energy can enhance the NLO responses. As a result of the reversible one-electron oxidizations of these systems, the redox switching of the NLO responses of systems 1a–5a have also been studied. The βtot value of system 2b′ is about 20.75 times larger than that of 2a due to the larger degree of conjugation, which provides a possibility of NLO switching. According to the analysis of the frontier molecular orbitals (FMO), oxidization reduces the HOMO–LUMO gap and changes charge transfer (CT) direction.
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40

Gan, Yong X., and Jeremy B. Gan. "Porous Fiber Processing and Manufacturing for Energy Storage Applications." ChemEngineering 4, no. 4 (November 3, 2020): 59. http://dx.doi.org/10.3390/chemengineering4040059.

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The objective of this article is to provide an overview on the current development of micro- and nanoporous fiber processing and manufacturing technologies. Various methods for making micro- and nanoporous fibers including co-electrospinning, melt spinning, dry jet-wet quenching spinning, vapor deposition, template assisted deposition, electrochemical oxidization, and hydrothermal oxidization are presented. Comparison is made in terms of advantages and disadvantages of different routes for porous fiber processing. Characterization of the pore size, porosity, and specific area is introduced as well. Applications of porous fibers in various fields are discussed. The emphasis is put on their uses for energy storage components and devices including rechargeable batteries and supercapacitors.
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41

Shen, Dazhi, Jian Liu, Lihui Gan, Naizhong Huang, and Minnan Long. "Controllable synthesis of mesoporous titanosilicates for styrene oxidization using a nanocellulose template strategy." RSC Advances 7, no. 31 (2017): 19237–42. http://dx.doi.org/10.1039/c7ra01598d.

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Xu, Shao-Hua, Chao Zhang, Wei-Wei Wang, Bo-Yang Yu, and Jian Zhang. "Site-selective biotransformation of ursane triterpenes by Streptomyces griseus ATCC 13273." RSC Advances 7, no. 34 (2017): 20754–59. http://dx.doi.org/10.1039/c7ra01811h.

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43

Li, Xiao-Hui, Yi-Wei Liu, Ying Lu, Zhong Zhang, Hong-Rui Tian, Shu-Mei Liu, and Shu-Xia Liu. "A universal strategy for fabrication and morphology control of polyoxometalate-based metal–organic frameworks." Chemical Communications 56, no. 11 (2020): 1641–44. http://dx.doi.org/10.1039/c9cc09554c.

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Wang, Yanqing, Yuemeng Li, Liping Ding, Xi Xu, Zhe Chen, Chaojiang Li, and Jun Ding. "Robust and superwetting island-shaped phytate bimetallic oxyhydroxide porous nanoclusters via a mild self-assembly—etching–catching—electrochemical oxidization strategy for an enhanced oxygen evolution reaction." Chemical Communications 55, no. 31 (2019): 4503–6. http://dx.doi.org/10.1039/c9cc00749k.

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Li, Jiao, Xinyu Fan, Yanpei Wei, Jinxiang Liu, Jinghua Guo, Xiaoxue Li, Vei Wang, Yunye Liang, and Gang Chen. "Voltage-gated spin-filtering properties and global minimum of planar MnB6, and half-metallicity and room-temperature ferromagnetism of its oxide sheet." Journal of Materials Chemistry C 4, no. 46 (2016): 10866–75. http://dx.doi.org/10.1039/c6tc03584a.

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Yang, Tao, Yihui Wang, Wenxian Wei, Xinran Ding, Maoshuai He, Tingting Yu, Hong Zhao, and Dongen Zhang. "Synthesis of octahedral Pt–Ni–Ir yolk–shell nanoparticles and their catalysis in oxygen reduction and methanol oxidization under both acidic and alkaline conditions." Nanoscale 11, no. 48 (2019): 23206–16. http://dx.doi.org/10.1039/c9nr07235g.

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Xie, Zhengwei, Zuolong Yu, Weifeng Fan, Gongchang Peng, and Meizhen Qu. "Effects of functional groups of graphene oxide on the electrochemical performance of lithium-ion batteries." RSC Advances 5, no. 109 (2015): 90041–48. http://dx.doi.org/10.1039/c5ra17854a.

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Li, Hao, Lei Song, Baohong Han, and Hongwei Song. "Improved sludge dewaterability using persulfate activated by humic acid supported nanoscale zero-valent iron: effect on sludge characteristics and reaction mechanisms." Environmental Science: Water Research & Technology 4, no. 10 (2018): 1480–88. http://dx.doi.org/10.1039/c8ew00379c.

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Liu, Xu Dong, Xiao Guo Bi, Wei Niu, Xin Guan, and Ying Nan Dong. "Study on Kinetics Behavior of the Lead Negative Electrode in the Lead Acid Flow Battery." Advanced Materials Research 608-609 (December 2012): 1012–16. http://dx.doi.org/10.4028/www.scientific.net/amr.608-609.1012.

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Abstract:
The chemistry system with negative graphite felt electrode and a single electrolyte, lead(II)in methanesulfonic acid, was described. The effects of treatment methods on kinetics and cyclic voltammetry behavior of Pb(II)/Pb couple were studied. The results show that the equilibrium electrode potential Pb(II)/Pb couple was -0.233V and the Pb(II)/Pb couple on graphite felt electrode had a good kinetics behavior. The cyclic voltammogram of graphite felt electrode showed that the oxidization and reduction peak potentials were -0.044V and -0.454V, respectively. The graphite felt treated with methanesulfonic acid had little oxidization and reduction peak potentials difference, and showed good electro-catalytic activity for Pb(II)/Pb couple.
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Li, Fang, Yuejiao Chen, and Jianmin Ma. "Porous SnO2 nanoplates for highly sensitive NO detection." J. Mater. Chem. A 2, no. 20 (2014): 7175–78. http://dx.doi.org/10.1039/c4ta00247d.

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