Thermally stable coordination compounds intercalated in montmorillonite clay mineral

1992 ◽  
Vol 70 (7) ◽  
pp. 1927-1931 ◽  
Author(s):  
N. K. Labhsetwar ◽  
O. P. Shrivastava
Keyword(s):  
Clay Mineral ◽  
Coordination Compounds ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Magnetic Studies ◽  
Swelling Properties ◽  
X Ray ◽  
Good Thermal Stability ◽  
Intercalated Compounds ◽  
Layered Clay

Montmorillonite is a natural layered clay mineral having myriad applications due mainly to its remarkable ion exchange, intercalation, and swelling properties. It can act as a good host for several compounds. Two intercalated coordination compounds of Cu(II) and Ni(II) with 2,2′-bipyridyl have been prepared in the interlayer spaces of montmorillonite structure. They are characterized on the basis of elemental analysis, infrared spectroscopy, magnetic studies, and X-ray diffraction. Both compounds show similarity in their structure and properties with the respective normal complexes of similar composition. These compounds show good thermal stability. The present intercalated compounds might be useful for their nitrogen-immobilizing properties and high-temperature applications.

scholarly journals Study of structures and properties of ZnO-Sb2O3-P2O5-Na2O glasses

2014 ◽  
Vol 32 (3) ◽  
pp. 414-418 ◽  
Author(s):  
Yajun Qi ◽  
Zhiqiang Wang ◽  
Shangru Zhai ◽  
Shuwen Jiang ◽  
Hai Lin
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Weight Loss ◽  
Deionized Water ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Structures And Properties ◽  
Thermal Stability Of

AbstractThe influence of ZnO substitution by 0–12 wt.% Na2O on the properties of ZnO-Sb2O3-P2O5-Na2O glasses has been investigated. The structure and properties of the glasses with the composition of (13.86-x)ZnO-57.93Sb2O3-28.21P2O5−x Na2O (x = 0–12 wt.%) were characterized by infrared spectra (IR), X-ray diffraction and differential thermal analysis (DTA). The results of IR indicated an increase in the intensity of symmetric vibrations of P-O-P bond, which was confirmed by the improvement of water durability with the increasing amount of Na2O in the range of 0–10 wt.%. Substitution of 10 wt.% Na2O led to the weight loss of the glass to 5.93 mg/cm−2 after immersion in deionized water at 50 °C for 24 h. The results of XRD showed that the ability of crystallization decreased, indicating the good thermal stability of the glass. The glass containing 8 wt.% Na2O had the best properties in every respect and might be an alternative to lead based glasses for the applications, providing further composition improvement.

High Resolution Replication of Organoclay Surfaces

1982 ◽  
Vol 40 ◽  
pp. 576-577
Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys
Keyword(s):  
Clay Mineral ◽  
Organic Molecule ◽  
Organic Molecules ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Naturally Occurring ◽  
Silicate Layers ◽  
Mineral Identification

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.

Microstructure and Physical Properties of Clay-Polymer Composites

2000 ◽  
Vol 628 ◽  
Author(s):  
T.N. Blanton ◽  
D. Majumdar ◽  
S.M. Melpolder
Keyword(s):  
Composite Materials ◽  
Physical Properties ◽  
Polymer Composites ◽  
Basal Plane ◽  
X Ray Diffraction ◽  
X Ray ◽  
Layered Clay

ABSTRACTClay-polymer nanoparticulate composite materials are evaluated by the X-ray diffraction technique. The basal plane spacing provided information about the degree of intercalation and exfoliation of the 2: 1 layered clay structure. Both intercalation and exfoliation are controlled by the identity of the polymer and the clay:polymer ratio.

Evolution structurale de la nacrite en fonction de la nature des molécules organiques intercalees

2000 ◽  
Vol 33 (6) ◽  
pp. 1351-1359 ◽  
Author(s):  
A. Ben Haj Amara ◽  
H. Ben Rhaiem ◽  
A. Plançon
Keyword(s):  
Ir Spectroscopy ◽  
Hydrogen Bonds ◽  
Dimethyl Sulfoxide ◽  
Organic Molecules ◽  
Interlayer Space ◽  
X Ray Diffraction ◽  
X Ray ◽  
Intercalated Compounds ◽  
Xrd Study ◽  
Intercalation Process

Nacrite has been intercalated with two polar organic molecules: dimethyl sulfoxide (DMSO) andN-methylacetamide (NMA). The homogeneous nacrite complexes have been studied by X-ray diffraction (XRD) and infrared (IR) spectroscopy. The XRD study is based on a comparison between experimental and calculated patterns. The structures of the intercalated compounds have been determined, including the mutual positions of the layers after intercalation and the positions of the intercalated molecules in the interlayer space. It has been shown that the intercalation process causes not only a swelling of the interlayer space but also a shift in the mutual in-plane positions of the layers. This shift depends on the nature of the intercalated molecules and is related to their shape and the hydrogen bonds which are established with the surrounding surfaces. For a given molecule, the intercalation process is the same for the different polytypes of the kaolinite family. These XRD results are consistent with those of IR spectroscopy.

Effect of the Pulse Laser Radiation on the Stabilization of the ZrO2 and HFO2 High-Temperature Phases

2015 ◽  
Vol 245 ◽  
pp. 200-203 ◽  
Author(s):  
Maxim Alexandrovich Pugachevskii ◽  
Viktor Igorevich Panfilov
Keyword(s):  
High Temperature ◽  
Transmission Electron Microscopy Data ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Quantitative Content ◽  
Electron Microscopy Data ◽  
Cubic Phases ◽  
Transmission Electron ◽  
Microscopy Data

The conditions of formation of the ZrO2 and HfO2 high-temperature (tetragonal and cubic) phases in the ablated nanoparticles were investigated. X-ray diffraction and transmission electron microscopy data demonstrate that laser intensities above 109 W/m2 ensure the formation of the ZrO2 high-temperature phases, while intensities above 5·109 W/m2 do the formation of the HfO2 high-temperature phases. Quantitative content of the high-temperature phases in layers of the ablated nanoparticles increases with raising the intensity. The obtained nanoparticles exhibit good thermal stability.

scholarly journals Synthesis, Structure, and Properties of a Dinuclear Cu(II) Coordination Polymer Based on Quinoxaline and 3,3-Thiodipropionic Acid Ligands

2021 ◽  
Author(s):  
Adedibu Clement Tella ◽  
Samson Owalude ◽  
Vincent Adimula ◽  
Adetola Oladipo ◽  
Victoria Olayemi ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Nitrogen Atom ◽  
Coordination Polymer ◽  
Elemental Analysis ◽  
Catalytic Reduction ◽  
Copper Acetate ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
H Nmr

Abstract The coordination polymer [Cu2(TDPH)4(QNX)].DMF, (QNX = Quinoxaline; TDPH = 3,3-thiodipropionic acid), has been prepared by reaction of copper acetate, TDPH, and quinoxaline. The compound was characterized by elemental analysis, FTIR spectroscopy, and single-crystal X-ray diffraction. The crystal is monoclinic with a P21/n space group and dimensions of a = 12.889(3) Å, b = 14.983(4) Å, c = 14.091(3) Å, α = 90 °, β = 90.200(11) °, γ = 90 °, V = 2721.18 (2) Å3, Z = 4. The ligands are hexagonally coordinated to the Cu(II) centre in the form of Cu2O4N with one nitrogen atom from the quinoxaline ligand, and four oxygen atoms from four TDPH molecules in a monodentate fashion. The Cu-Cu bond length was 2.642(1) and 2.629(1) Å for the Cu1----Cu1 and Cu2----Cu2 bonds. The QNX ligand bridged the two copper atoms. The catalytic reduction of 4-nitrophenol to 4-aminophenol using NaBH4 in the presence of [Cu2(TDPH)4(QNX)].DMF, as catalyst was completed within 11 minutes. The 4-aminophenol product was confirmed using 1H NMR spectroscopy.

New Developments for Lignocellulosics-Nanocomposites with Low Carbon Footprint

2012 ◽  
Vol 1386 ◽  
Author(s):  
Alcides L. Leao ◽  
Bibin M. Cherian ◽  
Sivoney F. Souza ◽  
Mohini Sain ◽  
Suresh Narine
Keyword(s):  
Cellulose Nanofibrils ◽  
Structure And Properties ◽  
Low Carbon ◽  
X Ray Diffraction ◽  
Fiber Morphology ◽  
Chemical Purification ◽  
New Developments ◽  
X Ray ◽  
Reinforcement Material ◽  
Microscopy Techniques

ABSTRACTCellulose nanofibrils have been evaluated as reinforcement material in polymeric matrixes due to their potential to improve the mechanical, optical, and dielectric properties of these matrixes as well as its environmental positive footprint. This work describes how banana nanocellulose can be used to replace others not so friendly materials in many applications including, biomaterials, automotive industries and packaging by proved with their mechanical properties. The process used is very mild to the environment and consists of a high pressure fibrillation followed by a chemical purification which affects the fiber morphology. Many fibers characterization processes were used including microscopy techniques and X-ray diffraction to study the structure and properties of the prepared nanofibers and composites. Microscopy studies showed that the used individualization processes lead to a unique morphology of interconnected web-like structure of the fibers.

Preparation, and complexes with nickel(II) and copper(II), of a diazepane amine alcohol. The structure of [4,4-dimethyl-7-(5,5,7-trimethyl-1,4-diazepan-1-yl)-5-azaheptan-2-ol]nickel(II) perchlorate

1983 ◽  
Vol 36 (7) ◽  
pp. 1341 ◽  
Author(s):  
KR Morgan ◽  
GJ Gainsford ◽  
NF Curtis
Keyword(s):  
Ground State ◽  
Coordination Compounds ◽  
Major Product ◽  
Boat Conformation ◽  
Singlet Ground State ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxygen Donor ◽  
Square Planar ◽  
Coordination Plane

Reduction of 4,4,12,12-tetramethyl-5,8,11-triazapentadecane-2,14-dione diperchlorate by sodium borohydride yields as the major product one isomer of 4,4-dimethyl-7-(5,5,7-trimethyl-1,2-diazepam 1-yl)-5-azaheptan-2-ol, pyaz. The coordination compounds [M(pyaz)] (ClO4), and [Ni(pyaz)(NCS)] CNS (M = NiII, CuII) were prepared, the latter being assigned five-coordinate structures. The structure of singlet ground state [Ni(pyaz)] (ClO4)2 was determined by X-ray diffraction [space group P212121, Z 4, a 1450.8(2), b 1522.2(1), c 1048.5(1) pm, R 0.0675, Rw 0.0768 for 2461 reflections]. The compound has a square-planar coordination arrangement, with the three nitrogen and the oxygen donor atoms of the pyaz ligand approximately coplanar [Ni-O 190.0(6) pm; Ni-N 192.8(6), 189.2(6), 189.2(6) pm in sequence N(5) of chain, N(l), N(4) of diazepane]. The diazepane ring adopts a boat conformation. One side of the nickel(II) coordination plane is sterically crowded by the presence of two axial methyl substituents. The ligand has two non-equivalent chiral centres (C(14) of the diazepane ring and C(2) of the amine alcohol chain), both present in the R configuration in the crystal studied. The three nitrogen atoms, which became chiral centres upon coordination, are present in the S configuration for two diazepane nitrogen atoms and in the R configuration for the 5-aza chain nitrogen.

Synthesis, crystal structure and properties of a 2-D Cd(II) coordination polymer based on ferrocenecarboxylate and 4,4′-bipyridine ligands

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Kai-Long Zhong ◽  
Jing Quan ◽  
Xian-Xiao Pan ◽  
Wei Song ◽  
Bing-Feng Li
Keyword(s):  
Coordination Polymer ◽  
Gravimetric Analysis ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Carboxylate Oxygen ◽  
Oxygen Chain ◽  
Crystal Structural

Abstract A new cadmium(II)-based coordination polymer [Cd3(FcCOO)6(4,4′-bipy)(H2O)2] n (FcCOO = ferrocenecarboxylato and 4,4′-bipy = 4,4′-bipyridine) has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The results of a crystal structural analysis has revealed that the title compound consists of two crystallographically unique CdII centers, one in a general position with a five-coordinated and one on an inversion center with a six-coordinated environment. The CdII centers are connected by FcCOO− units to form a metal carboxylate oxygen chain extending parallel to the [100] direction while the 4,4′-bipy ligands further act as bridging linkers of the CdII centers resulting in a layered polymer. In addition, an X-ray powder diffraction and thermal gravimetric analysis and a cyclo-voltammetric characterization of the complex have also been carried out.

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