scholarly journals Volumetric Source Model to Predict Productivity of Fractured Horizontal Well in Naturally Fractured Reservoirs

2015 ◽  
Vol 8 (1) ◽  
pp. 373-384 ◽  
Author(s):  
Tianhui Wang ◽  
Haitao Li ◽  
Junchao Wang ◽  
Yunlin Jia ◽  
Lifeng Liu
Keyword(s):  
Horizontal Well ◽  
Fractured Reservoirs ◽  
Source Model ◽  
Naturally Fractured Reservoirs ◽  
X Ray Diffraction ◽  
Cyclic Voltammetric ◽  
X Ray ◽  
Trigonal Bipyramidal ◽  
Fractured Horizontal Well ◽  
Square Planar

A novel dinuclear Cu(II) complex material has been synthesized by the reaction of 1, 2-phenylenedioxydiacetic acid, 1,10-phenantroline (phen) and Cu(CHCOO)·HO. And it has been characterized by elemental analysis, IR, UV and single crystal X-ray diffraction. The crystal belongs to tetragonal, space group I4/ with = = 25.381(4) Å, = 32.044(6) Å, = 20643(6) Å, = 16, D= 1.395 g·cm, = 0.898 mm, (000) = 8896, and final = 0.1026, = 0.3142. The structural analysis shows that two Cu(II) atoms adopt different coordination modes, Cu has five-coordination with a trigonal bipyramidal configuration, and Cu has four-coordination with a distorted square planar configuration. The cyclic voltammetric behaviour of the dinuclear Cu(II) complex has been investigated.

scholarly journals Synthesis, Structural Characterization and Electrochemical Property of a Dinuclear Cu (II) Complex Material

2015 ◽  
Vol 9 (1) ◽  
pp. 210-213
Author(s):  
Xi-Shi Tai ◽  
Xin Wang ◽  
Li Liu
Keyword(s):  
Structural Analysis ◽  
Electrochemical Property ◽  
Structural Characterization ◽  
X Ray Diffraction ◽  
Cyclic Voltammetric ◽  
Complex Material ◽  
X Ray ◽  
Planar Configuration ◽  
Trigonal Bipyramidal ◽  
Square Planar

A novel dinuclear Cu(II) complex material has been synthesized by the reaction of 1, 2-phenylenedioxydiacetic acid, 1,10-phenantroline (phen) and Cu(CH3COO)2·H2O. And it has been characterized by elemental analysis, IR, UV and single crystal X-ray diffraction. The crystal belongs to tetragonal, space group I41/a with a = b = 25.381(4) Å,c = 32.044(6) Å, V= 20643(6) Å3, = 16, Dc= 1.395 g·cm-3, µ = 0.898 mm, F (000) = 8896, and final R = 0.1026, ωR = 0.3142. The structural analysis shows that two Cu(II) atoms adopt different coordination modes, Cu1 has five-coordination with a trigonal bipyramidal configuration, and Cu2 has four-coordination with a distorted square planar configuration. The cyclic voltammetric behaviour of the dinuclear Cu(II) complex has been investigated.

scholarly journals A New Model to Predict Productivity of Multiple-Fractured Horizontal Well in Naturally Fractured Reservoirs

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Junchao Wang ◽  
Haitao Li ◽  
Yongqing Wang ◽  
Ying Li ◽  
Beibei Jiang ◽  
...  
Keyword(s):  
Flow Rate ◽  
Horizontal Well ◽  
Fractured Reservoirs ◽  
Orthogonal Transformation ◽  
Naturally Fractured Reservoirs ◽  
Hydraulic Fractures ◽  
Fractured Reservoir ◽  
Flow Models ◽  
Fractured Horizontal Well ◽  
Influent Factors

In order to predict productivity of multiple-fractured horizontal well in fractured reservoir, flow models of reservoir and hydraulic fractures based on the volumetric source idealization are developed. The models are solved by utilizing Laplace transformation and orthogonal transformation, and flow rate of the well is calculated by coupling the two models. Compared to traditional point source functions, volumetric source function has many advantages in properties of function and programming calculation. The productivity predicting model is verified via an analytical ternary-porosity model. Moreover, a practical example of fractured horizontal well is studied to analyze the productivity and its influent factors. The result shows that flow rate of each fracture is different and inner fracture contributes least to productivity. Meanwhile, there are optimizing ranges for number, length, and conductivity of hydraulic fractures. In low-permeability reservoir, increasing surface area in contact with reservoir by increasing number and length of hydraulic fractures is the most effective method to improve the productivity.

Synthesis and Structure of a Clathrated Two-Dimensional Metal-Organic Framework: [Cd(4,4'-bpy)2(H2O)2](ClO4)2·(L)2·H2O (L = Bis(1-pyrazinylethylidene)hydrazine)

2008 ◽  
Vol 73 (1) ◽  
pp. 24-31
Author(s):  
Dayu Wu ◽  
Genhua Wu ◽  
Wei Huang ◽  
Zhuqing Wang
Keyword(s):  
Metal Organic Framework ◽  
Channel Structure ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Guest Molecules ◽  
X Ray ◽  
Square Planar ◽  
Metal Organic ◽  
Aqueous Meoh ◽  
Organic Framework

The compound [Cd(4,4'-bpy)2(H2O)2](ClO4)2·(L)2 was obtained by the reaction of Cd(ClO4)2, bis(1-pyrazinylethylidene)hydrazine (L) and 4,4'-bipyridine in aqueous MeOH. Single-crystal X-ray diffraction has revealed its two-dimensional metal-organic framework. The 2-D layers superpose on each other, giving a channel structure. The square planar grids consist of two pairs of shared edges with Cd(II) ion and a 4,4'-bipyridine molecule each vertex and side, respectively. The square cavity has a dimension of 11.817 × 11.781 Å. Two guest molecules of bis(1-pyrazinylethylidene)hydrazine are clathrated in every hydrophobic host cavity, being further stabilized by π-π stacking and hydrogen bonding. The results suggest that the hydrazine molecules present in the network serve as structure-directing templates in the formation of crystal structures.

Crystal and molecular structure of diorganoammonium oxalatotrimethylstannate, [R2NH2][Me3Sn(C2O4)] (R=i-Bu, cyclohexyl)

2011 ◽  
Vol 34 (5-6) ◽  
pp. 127-130 ◽  
Author(s):  
Yaya Sow ◽  
Libasse Diop ◽  
Kieran C. Molloy ◽  
Gabrielle Kociok-Köhn
Keyword(s):  
Molecular Structure ◽  
Hydrogen Bonds ◽  
Diffraction Study ◽  
Crystal And Molecular Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Trigonal Bipyramidal ◽  
Trans Complex ◽  
A Chain ◽  
Distorted Trigonal Bipyramidal

Abstract The title compounds [R2NH2][C2O4SnMe3](R=i-Bu, Cy), in which tin atoms adopt a distorted trigonal bipyramidal configuration, have been prepared and submitted to an X-ray diffraction study. These compounds have been obtained from the reaction of (Cy2NH2)2C2O4·H2O or (i-Bu2NH2)2C2O4 with SnMe3Cl. In both [R2NH2][C2O4SnMe3] compounds, the trans complex has an almost regular trigonal bipyramidal geometry around the tin atom. The SnMe3 residues are connected as a chain with bridging oxalate anions in a trans-SnC3O2 framework, the oxygen atoms being in axial positions. The cations connect linear adjacent chains through NH…O hydrogen bonds giving layered structures.

scholarly journals Crystal and molecular structure and 31P and 195Pt nmr spectroscopy of [Pt3S2(PMe2Ph)6][BEt4]2; a trinuclear complex containing triply-bridging sulphide ligands

1984 ◽  
Vol 62 (4) ◽  
pp. 696-702 ◽  
Author(s):  
Gordon William Bushnell ◽  
Keith Roger Dixon ◽  
Reiko Ono ◽  
Alan Pidcock
Keyword(s):  
Trinuclear Complex ◽  
Complete Analysis ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Interactions ◽  
Nuclear Magnetic Resonance Spectra ◽  
Square Planar ◽  
Metal Metal ◽  
Pd Complexes

An X-ray diffraction study of [Pt3S2(PMe2Ph)6][BEt4]2 shows that it crystallises in the monoclinic space group, C2/c, with a = 15.447(2), b = 18.033(3), c = 26.505(5) Å, β = 96.73(2)°. The cation consists of three, distorted, square-planar cis-PtS2(PMe2Ph)2 moieties combined by sharing of the two sulphur atoms to produce a central Pt3S2 unit with C2 symmetry and Pt—Pt distances of 3.182(1) Å (one edge) and 3.108(1) Å (two edges). Complete analysis and computer simulation of 31P{1H} and 195Pt{1H} nuclear magnetic resonance spectra give values for 1J(Pt—P), 3202 Hz; 3J(Pt—P), −25 Hz; and 2J(Pt—Pt), 476 Hz. The structure is compared with previous results for analogous Ni and Pd complexes and the structural and nmr parameters are discussed with reference to the possibility of metal–metal interactions.

The molecular and crystal structure of [Pt(diethylenetriamine)(guanosine)](ClO4)2

1979 ◽  
Vol 57 (1) ◽  
pp. 57-61 ◽  
Author(s):  
R. Melanson ◽  
F. D. Rochon
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Least Squares ◽  
Platinum Atom ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
R Factor ◽  
Square Planar ◽  
Coordination Plane

The crystal structure of [Pt(diethylenetriamine)(guanosine)](ClO4)2 has been determined by X-ray diffraction. The crystals are orthorhombic, space group P212121, with a = 12.486(6), b = 13.444(7), c = 14.678(11) Å, and Z = 4. The structure was refined by block-diagonal least-squares analysis to a conventional R factor of 0.050 and a weighted Rw = 0.045.The coordination around the platinum atom is square planar. Guanosine is bonded to platinum through N(7). The purine planar ring makes an angle of 62.7° with the platinum coordination plane. The structure is stabilized by hydrogen bonding.

scholarly journals A Covalent Organic Cage Compound Acting as a Supramolecular Shadow Mask for the Regioselective Functionalization of C60

2020 ◽  
Author(s):  
Viktoria Leonhardt ◽  
Stefanie Fimmel ◽  
Ana-Maria Krause ◽  
Florian Beuerle
Keyword(s):  
Mass Spectrometry ◽  
Single Crystal ◽  
High Selectivity ◽  
Shadow Mask ◽  
X Ray Diffraction ◽  
X Ray ◽  
Trigonal Bipyramidal ◽  
Cage Compound ◽  
Vis Spectroscopy ◽  
Regioselective Functionalization

<div><div><div><p>A trigonal-bipyramidal covalent organic cage compound serves as an efficient host to form stable 1:1-complexes with C60 and C70. Fullerene encapsulation has been comprehensively studied by NMR and UV/Vis spectroscopy, mass spectrometry as well as single-crystal X-ray diffraction. Exohedral functionalization of encapsulated C60 via threefold Prato reaction revealed high selectivity for the symmetry-matched all-trans-3 addition pattern.</p></div></div></div>

scholarly journals Copper(II) and Zinc(II) Complexes Derived from N,N’-Bis(4-bromosalicylidene)propane-1,3-diamine: Syntheses, Crystal Structures and Antimicrobial Activity

2021 ◽  
Vol 68 (1) ◽  
pp. 102-108
Author(s):  
Yu-Mei Hao
Keyword(s):  
Escherichia Coli ◽  
Antimicrobial Activity ◽  
Candida Parapsilosis ◽  
Antibacterial Activities ◽  
X Ray Diffraction ◽  
Deprotonated Form ◽  
X Ray ◽  
Square Planar ◽  
Vis Spectroscopy ◽  
Elemental Analyses

A mononuclear copper(II) complex, [CuL] (1), and a phenolato-bridged trinuclear zinc(II) complex, [Zn3Cl2L2(DMF)2] (2), where L is the deprotonated form of N,N’-bis(4-bromosalicylidene)propane-1,3-diamine (H2L), have been prepared and characterized by elemental analyses, IR and UV-Vis spectroscopy, and single crystal X-ray diffraction. The Cu atom in complex 1 is in square planar coordination, while the terminal and central Zn atoms in complex 2 are in square pyramidal and octahedral coordination, respectively. The antibacterial activities of the complexes have been tested on the bacteria Staphylococcus aureus and Escherichia coli, and the yeast Candida parapsilosis.

scholarly journals Crystal structure refinement of magnesium zinc divanadate, MgZnV2O7, from powder X-ray diffraction data

2021 ◽  
Vol 77 (6) ◽  
pp. 588-591
Author(s):  
Stephanie J. Hong ◽  
Jun Li ◽  
Mas A. Subramanian
Keyword(s):  
Crystal Structure ◽  
Diffraction Data ◽  
Structure Refinement ◽  
Atomic Ratio ◽  
Asymmetric Unit ◽  
X Ray Diffraction ◽  
X Ray ◽  
Trigonal Bipyramidal ◽  
Wyckoff Position ◽  
Distorted Trigonal Bipyramidal

The crystal structure of magnesium zinc divanadate, MgZnV2O7, was determined and refined from laboratory X-ray powder diffraction data. The title compound was synthesized by a solid-state reaction at 1023 K in air. The crystal structure is isotypic with Mn0.6Zn1.4V2O7 (C2/m; Z = 6) and is related to the crystal structure of thortveitite. The asymmetric unit contains two metal sites with statistically distributed magnesium and zinc atoms with the atomic ratio close to 1:1. One (Mg/Zn) metal site (M1) is located on Wyckoff position 8j and the other (M2) on 4h. Three V sites (all on 4i), and eight O (three 8j, four 4i, and one 2b) sites complete the asymmetric unit. The structure is an alternate stacking of V2O7 layers and (Mg/Zn) atom layers along [20\overline{1}]. It is distinct from other related structures in that each V2O7 layer consists of two groups: a V2O7 dimer and a V4O14 tetramer. Mixed-occupied M1 and M2 are coordinated by oxygen atoms in distorted trigonal bipyramidal and octahedral sites, respectively.

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