Study on the Loadings of Co3O4 Supported on rGO as the Catalyst for Degradation of Orange II in Water by AOPs Based on Sulfate Radicals

2014 ◽  
Vol 955-959 ◽  
pp. 62-65 ◽  
Author(s):  
Peng Hui Shi ◽  
Hon Gai Zheng ◽  
Wei Feng Yao ◽  
Qiang Wu ◽  
Si Yu Tan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Catalytic Activity ◽  
Cobalt Oxide ◽  
Orange Ii ◽  
X Ray Diffraction ◽  
Sulfate Radicals ◽  
X Ray ◽  
Reduced Graphene

A variety of loadings of Cobalt oxide (Co3O4) was successfully supported on the reduced graphene (Co3O4/rGO) as the catalyst to activate peroxymonosulfate (PMS) to generate sulfate radicals (SO4−•) for degrading Orange II in water. The crystal structure of Co3O4/rGO with different loadings was characterized by X-ray diffraction (XRD), and their catalytic activity was compared in the same conditions. The result showed that the catalyst has an optimum Co3O4 loading. Using the 70.7% loading of Co3O4 in Co3O4/rGO as the catalyst, 100% decomposition could be achieved within 4 min with 1 mM Orange II, 0.05g/L catalyst, and 10 mM PMS.

Synthesis of Co3O4/RGO as Catalyst for Degradation of Orange II in Water by Advanced Oxidation Processes Based on Sulfate Radicals

2012 ◽  
Vol 534 ◽  
pp. 269-272 ◽  
Author(s):  
Peng Hui Shi ◽  
Shao Bo Zhu ◽  
Rui Jing Su ◽  
Jin Tao Ren ◽  
Deng Xin Li ◽  
...  
Keyword(s):  
Advanced Oxidation Processes ◽  
Advanced Oxidation ◽  
High Catalytic Activity ◽  
Orange Ii ◽  
X Ray Diffraction ◽  
Sulfate Radicals ◽  
X Ray ◽  
Oxidation Processes ◽  
Reduced Graphene ◽  
One Step

One step synthesis reduced graphene oxide and cobalt oxides nanocomposites (Co3O4/RGO) in ethylene glycol as heterogeneous catalyst. The Co3O4/RGO was confirmed by X-ray diffraction (XRD). And Co3O4/RGO exhibits an unexpected, surprisingly high catalytic activity in degradation of Orange II in water by advanced oxidation processes based on sulfate radicals and 100% decomposition could be achieved in 16 min.

scholarly journals Synthesis and catalytic activity of homoleptic lanthanide-tris(cyclopropylethinyl)amidinates

2015 ◽  
Vol 39 (10) ◽  
pp. 7595-7601 ◽  
Author(s):  
Farid M. Sroor ◽  
Cristian G. Hrib ◽  
Liane Hilfert ◽  
Sabine Busse ◽  
Frank T. Edelmann
Keyword(s):  
Crystal Structure ◽  
Catalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Type C

New unsolvated, homoleptic lanthanide(iii) tris(cyclopropylethinylamidinate) complexes of the type [c-C3H5–CC–C(NR)2]3Ln (R = iPr, cyclohexyl; Ln = Nd, Sm, Ho) have been prepared and the crystal structure of the holmium derivative [c-C3H5–CC–C(NiPr)2]3Ho has been confirmed by X-ray diffraction.

Synthesis, Characterization, and Crystal Structure of Several Novel Acidic Ionic Liquids: 1-ethyl-2-alkyl-benzimidazolium Tetra-Fluoroborate

2013 ◽  
Vol 457-458 ◽  
pp. 139-143 ◽  
Author(s):  
Ming Tian Wang ◽  
Chang Ping Pan ◽  
Wei Peng Gai ◽  
Xiao Xia Lv ◽  
Min Gang Zhai ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Ionic Liquid ◽  
Acetic Acid ◽  
Catalytic Activity ◽  
Lamellar Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Acidic Ionic Liquid ◽  
Acidic Ionic Liquids ◽  
Good Catalytic Activity

A series of novel acidic ionic liquid: 1-ethyl-2-alkyl-benzimidazolium tetra-fluoroborate (alkyl= Et, Pr-n, Bu-n) were prepared by simple acid-based neutralization of 1-ethyl-2-alkyl-benzimidazole and tetrafluoroboric acid. The compounds were characterized by FTIR spectra, elemental analysis,1HNMR spectra and thermogravimetric analysis. These novel tetra-fluoroborate salts show good catalytic activity to esterification of benzyl alcohol and acetic acid. Furthermore, a crystal of ([H-ebBiBF4) was prepared with the crystal structure and determined by X-ray diffraction analysis. The molecular is of lamellar structure as mainly π electron ring is stacked interleaving between two layers. The results of cation and anion arranged orderly in pair indicate that the coulombic attraction is more dominant. Simultaneously, the weak local hydrogen bonds C-H···F exist in the molecules.

Treatment of Dye Wastewater by Zero Valent Iron Composited Organobentonite

2011 ◽  
Vol 340 ◽  
pp. 229-235 ◽  
Author(s):  
Jian Feng Ma ◽  
Jian Ming Yu ◽  
Bing Ying Cui ◽  
Ding Long Li ◽  
Juan Dai
Keyword(s):  
Crystal Structure ◽  
Zero Valent Iron ◽  
Orange Ii ◽  
Dye Wastewater ◽  
Removal Mechanism ◽  
X Ray Diffraction ◽  
X Ray ◽  
Secondary Pollution ◽  
Novel Material ◽  
Adsorption Amount

A novel material, zero valent iron composited organobentonite (NZVI-OB), was synthesized to adsorb dye from wastewater and to degrade the dye for avoiding secondary pollution. The crystal structure was characterized with X-ray diffraction (XRD). The effect of initial Orange II concentration and reaction time on the removal of Orange II by the NZVI-OB was studied. And the removal mechanism of Orange II was discussed. The results show that the Orange II can be removed by NZVI-OB efficiently. The maximal adsorption amount is 112.66 mg/g. The iron can effectively degrade the organic compounds after adsorption pollution, the carbon contents of organic pollutions after catalyzed and oxidized by the iron are lowered to the 19% of the original.

Crystal structure of an inclusion complex between chiral monoaza-15-crown-5 and S(–)-1-phenyl-ethyl ammonium percholorate

2003 ◽  
Vol 218 (5) ◽  
Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Type

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group

Bis(μ-carboxylato)dienerhodium(I) Complexes - Synthesis, Characterization and Catalytic Activity

2008 ◽  
Vol 73 (8-9) ◽  
pp. 1205-1221 ◽  
Author(s):  
Jiří Zedník ◽  
Jan Sedláček ◽  
Jan Svoboda ◽  
Jiří Vohlídal ◽  
Dmitrij Bondarev ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffraction Analysis ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray

Dinuclear rhodium(I) η2:η2-cycloocta-1,5-diene (series a) and η2:η2-norborna-2,5-diene (series b) complexes with μ-RCOO- ligands, where R is linear C21H43 (complexes 1a, 1b), CH2CMe3 (2a, 2b), 1-adamantyl (3a, 3b) and benzyl (4a, 4b), have been prepared and characterized by spectroscopic methods. Structures of complexes 2b, 3a and 4a were determined by X-ray diffraction analysis. Complexes prepared show low to moderate catalytic activity in polymerization of phenylacetylene in THF giving high-cis-transoid polymers, but they show only oligomerization activity in dichloromethane.

Crystal Forms of Semisynthetic Ergot Alkaloid Terguride

2002 ◽  
Vol 67 (4) ◽  
pp. 479-489 ◽  
Author(s):  
Michal Hušák ◽  
Bohumil Kratochvíl ◽  
Ivana Císařová ◽  
Ladislav Cvak ◽  
Alexandr Jegorov ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Ergot Alkaloid ◽  
Simplified Model ◽  
Quantum Mechanical ◽  
Quantum Mechanical Calculations ◽  
X Ray Diffraction ◽  
Torsion Angles ◽  
Crystal Forms ◽  
X Ray ◽  
Independent Molecules

Two new structures of semisynthetic ergot alkaloid terguride created by unusual number of symmetry-independent molecules were determined by X-ray diffraction methods at 150 K. Form A (monoclinic, P212121, Z = 12) contains three symmetry-independent terguride molecules and two molecules of water in the asymmetric part of the unit cell. The form CA (monoclinic, P21, Z = 8) is an anhydrate remarkable by the presence of four symmetry-independent molecules in the crystal structure. Conformations of twelve symmetry-independent molecules that were found in four already described terguride structures are compared with torsion angles obtained by ab initio quantum-mechanical calculations for the simplified model of N-cyclohexyl-N'-diethylurea.

scholarly journals High-pressure synthesis and crystal structure of the mixed-cation borate Ga4In4B15O33(OH)3

2019 ◽  
Vol 74 (4) ◽  
pp. 357-363
Author(s):  
Daniela Vitzthum ◽  
Hubert Huppertz
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
High Temperature ◽  
Diffraction Data ◽  
X Ray Diffraction ◽  
Synthesis And Crystal Structure ◽  
X Ray ◽  
Mixed Cation ◽  
High Pressure High Temperature ◽  
Pressure Synthesis

AbstractThe mixed cation triel borate Ga4In4B15O33(OH)3 was synthesized in a Walker-type multianvil apparatus at high-pressure/high-temperature conditions of 12.5 GPa and 1300°C. Although the product could not be reproduced in further experiments, its crystal structure could be reliably determined via single-crystal X-ray diffraction data. Ga4In4B15O33(OH)3 crystallizes in the tetragonal space group I41/a (origin choice 2) with the lattice parameters a = 11.382(2), c = 15.244(2) Å, and V = 1974.9(4) Å3. The structure of the quaternary triel borate consists of a complex network of BO4 tetrahedra, edge-sharing InO6 octahedra in dinuclear units, and very dense edge-sharing GaO6 octahedra in tetranuclear units.

Crystal structure determination of the conformation of two bicyclo[3.3.1]nonan-ones

1985 ◽  
Vol 63 (6) ◽  
pp. 1166-1169 ◽  
Author(s):  
John F. Richardson ◽  
Ted S. Sorensen
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Chair Conformation ◽  
Molecular Structures ◽  
Boat Conformation ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Final Agreement

The molecular structures of exo-7-methylbicyclo[3.3.1]nonan-3-one, 3, and the endo-7-methyl isomer, 4, have been determined using X-ray-diffraction techniques. Compound 3 crystallizes in the space group [Formula: see text] with a = 15.115(1), c = 7.677(2) Å, and Z = 8 while 4 crystallizes in the space group P21 with a = 6.446(1), b = 7.831(1), c = 8.414(2) Å, β = 94.42(2)°, and Z = 2. The structures were solved by direct methods and refined to final agreement factors of R = 0.041 and R = 0.034 for 3 and 4 respectively. Compound 3 exists in a chair–chair conformation and there is no significant flattening of the chair rings. However, in 4, the non-ketone ring is forced into a boat conformation. These results are significant in interpreting what conformations may be present in the related sp2-hybridized carbocations.

Sign in / Sign up

Export Citation Format

Share Document