Structure characterization of the non-crystalline complexes of copper salts with native cyclodextrins

2016 ◽  
Vol 45 (26) ◽  
pp. 10696-10707 ◽  
Author(s):  
Manuel I. Velasco ◽  
Claudio R. Krapacher ◽  
Rita H. de Rossi ◽  
Laura I. Rossi
Keyword(s):  
Physicochemical Properties ◽  
Coordination Compounds ◽  
Simple Procedure ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
Copper Salts ◽  
X Ray ◽  
Ft Ir ◽  
Crystalline Complexes Of

The characterization of non-crystalline complexes is very difficult when techniques like X-ray diffraction or NMR are not available. We propose a simple procedure to characterize the physicochemical properties of amorphous new coordination compounds between cyclodextrins (CD) and Cu2+ salts, by several techniques as TGA, FT-IR, EPR.

Synthesis and Characterization of the Layered Zirconium Phosphate and its Intercalation Study

2011 ◽  
Vol 233-235 ◽  
pp. 1809-1813
Author(s):  
Yu Ping Tong ◽  
Chang Li Xiao ◽  
Zhong Zheng Yang ◽  
Lu De Lu ◽  
Hao Bing Fu
Keyword(s):  
Zirconium Phosphate ◽  
Structure Characterization ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Tetramethylammonium Bromide ◽  
Ft Ir ◽  
Transition Electron ◽  
Ft Raman

The zirconium phosphate α-Zr(HPO4)2·H2O (α-ZrP) with layered structure has been synthesized by refluxing method. Power X-ray diffraction (XRD), vibrational spectroscopy (FT-IR, FT-Raman), thermal analysis (TG-DSC), transition electron spectroscopy (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectrometer (EDS) was respectively used for structure characterization of the compound α-ZrP. The result of intercalation reactions with tetramethylammonium bromide and cetyltrimethylammonium bromide showed interlayer distances increase of ~ 0.46 nm and ~ 1.68 nm, respectively. The BET surface area of α-ZrP is 12.29 m2·g-1. The cyclic voltammetry behaviors of the compound on Au electrode showed a typical reversible process. Moreover, the strong fluorescent property of the α-ZrP was measured. The maximum emission peaks occurred at ca. 390 nm upon excitation at ca. 288 nm.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Microwave-assisted solvent-free synthesis and spectral and structural characterization of cyclotriphosphazene hexakis(o-tolylamide)

2018 ◽  
Vol 73 (12) ◽  
pp. 999-1003 ◽  
Author(s):  
Mohammad Hakimi ◽  
Homeyra Rezaei ◽  
Keyvan Moeini ◽  
Heidar Raissi ◽  
Vaclav Eigner ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Microwave Irradiation ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
Aromatic Rings ◽  
X Ray ◽  
Microwave Assisted ◽  
Ft Ir ◽  
Solvent Free Synthesis

AbstractA new cyclotriphosphazene, 2,2,4,4,6,6-hexakis (o-tolylamono)-1,3,5,2λ5,4λ5,6λ5-triazatriphosphinine (MPAP), was prepared using microwave irradiation and identified by elemental analysis, FT-IR, Raman, 31P NMR spectroscopy, and single-crystal X-ray diffraction. In the crystal, in addition to hydrogen bonds, the network is further stabilized by inter- and intramolecular π–π stacking interactions between aromatic rings.

Structure Characterization of Sintered CaO-Al2O3-SiO2 Glass-Ceramic Reinforced with Spodumene

2013 ◽  
Vol 834-836 ◽  
pp. 309-314
Author(s):  
Zi Fan Xiao ◽  
Jin Shu Cheng ◽  
Jun Xie
Keyword(s):  
Glass Ceramic ◽  
Energy Dispersive Spectrometry ◽  
Crystal Size ◽  
Bending Strength ◽  
Glass Ceramics ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
X Ray

A glass-ceramic belonging to the CaO-Al2O3-SiO2(CAS) system with different composition of spodumene and doping the Li2O with amount between 0~2.5 % (mass fraction) were prepared by onestage heat treatment, under sintering and crystallization temperature at 1120 °C for two hours. In this paper, differential thermal analysis, X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry and bending strength test were employed to investigate the microstructure and properties of all samples. β-wollastonite crystals were identified as the major crystalline phases, and increasing Li2O was found to be benefit for the crystallization and tiny crystalline phases remelting, resulting in the content of major crystalline phases increased first and then decreased with increasing the expense of spodumene. Meanwhile, the crystal size can be positively related with the content of Li2O. The preferable admixed dosage of spodumene can be obtained, besides the strength of glass-ceramics can be more than 90 MPa.

The Characterization of Bovine Bone-Derived Hydroxyapatite Isolated Using Novel Non-Hazardous Method

2020 ◽  
Vol 45 ◽  
pp. 49-56
Author(s):  
Aniek Setiya Budiatin ◽  
Samirah ◽  
Maria Apriliani Gani ◽  
Wenny Putri Nilamsari ◽  
Chrismawan Ardianto ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Extraction Method ◽  
Bovine Bone ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Novel Method ◽  
Scanning Electron

Bovine bone is a considerable source for the production of hydroxyapatite. The recent study reported a novel method to extract hydroxyapatite from bovine bone without producing hazardous residue. The bovine bones were cut and boiled in the opened chamber followed by boiling in pressurized tank. The bones were then soaked into 95% ethanol. Calcination was then conducted in 800°C, 900°C and 1,000°C, for 2 hours. The result was then grinded and sieved. The powder then was characterized using Fourier transform infrared (FT-IR), Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) to measure the purity of hydroxyapatite. It is concluded that the hydroxyapatite derived from this process showed 100% purity, resulting 35.34 ± 0.39% w/w from the wet bone weight and 72.3% w/w from the dried weight. The present extraction method has been proven to yield high amount of pure hydroxyapatite as well as reducing the use of hazardous reagent.

scholarly journals Synthesis, Crystal Structures, and Spectroscopic Characterization of Bis-aldehyde Monomers and Their Electrically Conductive Pristine Polyazomethines

Polymers ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1498 ◽  
Author(s):  
Abdul Hafeez ◽  
Zareen Akhter ◽  
John F. Gallagher ◽  
Nawazish Ali Khan ◽  
Asghari Gul ◽  
...  
Keyword(s):  
Electrical Conductivity ◽  
Spectroscopic Characterization ◽  
Spectroscopic Techniques ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
Electrically Conductive ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Ft Ir

Bis-aldehyde monomers 4-(4′-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4′-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4′-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4′-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal X-ray diffraction structures of 3b and 3c were determined. The structural characterization of the monomers and poly(azomethine)s was performed by FT-IR and NMR spectroscopic techniques and elemental analysis. Physicochemical properties of polymers were investigated by powder X-ray diffraction, thermogravimetric analysis (TGA), viscometry, UV–vis, spectroscopy and photoluminescence. These polymers were subjected to electrical conductivity measurements by the four-probe method, and their conductivities were found to be in the range 4.0 × 10−5 to 6.4 × 10−5 Scm−1, which was significantly higher than the values reported so far.

Characterization of Electrospun Poly(Lactic Acid)/polyaniline Blend Nanofibers

2011 ◽  
Vol 332-334 ◽  
pp. 317-320 ◽  
Author(s):  
Hui Qin Zhang
Keyword(s):  
Lactic Acid ◽  
Composite Nanofibers ◽  
Weight Ratio ◽  
Electrospinning Process ◽  
Poly Lactic Acid ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Ft Ir

In this study, composite nanofibers of polyaniline doped with dodecylbenzene sulfonic acid (PANI-DBSA) and Poly(lactic acid) (PLA) were prepared via an electrospinning process. The surface morphology, thermal properties and crystal structure of PLA/PANI-DBSA nanofibers are characterized using Fourier transform infrared spectroscopy (FT-IR), wide-angle x-ray diffraction (WAXD) and scanning electron microscopy (SEM). SEM images showed that the morphology and diameter of the nanofibers were affected by the weight ratio of blend solution.

Preparation and Electrical Characterization of Poly(Aniline) NanoClay Composites

2015 ◽  
Vol 34 (4) ◽  
Author(s):  
Esma Ahlatcioǧlu ◽  
Bahire Filiz şenkal ◽  
Mustafa Okutan
Keyword(s):  
Electrical Characterization ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Inorganic Hybrid ◽  
X Ray ◽  
Ft Ir ◽  
Doped Polyaniline ◽  
Poly Aniline ◽  
Scanning Electron

AbstractIn this work, synthesis and characterization of composite materials based on NanoClay(NC) and boric acid doped PolyAniline (PANI) is studied. PANI was successfully incorporated into NC to form PANI-NC composites. The resulting organic-inorganic hybrid material, PANI-NC was characterized by various physicochemical techniques. Formation of PANI inside the clay tactoid has been confirmed by X-ray diffraction studies (XRD), scanning electron microscope (SEM) and FT-IR. Also, conductivity and physical properties of the PANI-NC composites were investigated.

scholarly journals Synthesis of Silver Nanoparticles Using Muntingia Calabura L. Leaf Extract as Bioreductor and Applied as Glucose Nanosensor

2018 ◽  
Vol 34 (6) ◽  
pp. 3088-3094 ◽  
Author(s):  
Abdul Wahid Wahab ◽  
Abdul Karim ◽  
Nursiah La Nafie ◽  
Nurafni Nurafni ◽  
I. Wayan Sutapa
Keyword(s):  
Particle Size ◽  
Silver Nanoparticles ◽  
Reduction Method ◽  
Measurement Range ◽  
Structure Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Muntingia Calabura

Silver nanoparticles have been synthesized by reduction method using extract of Muntingia calabura L. leaf a bioreductor. The process of silver nanoparticles formation was monitored by UV-Vis method. The results showed that the absorbance values increased according to the increase of reaction time. Maximum absorption of silver nanoparticle was obtained at a wavelength of 41-421 nm. The size of silver nanoparticles was determined using a PSA (Particle Size Analyzer) with a particle size distribution of 97.04 nm. The functional groups compound that contribute in the synthesis was analyzed using Fourier Transform Infrared Spectroscopy (FTIR). Morphology of the silver nanoparticles was observed by an Scanning Electron Microscope instrument and the structure characterization of the compounds were analyzed using X-Ray Diffraction. The glucose nanosensor based on silver nanoparticles have the measurement range of 1 mM - 4 mM with the regretion (R2) is 0,9516, the detection limit of sensor is 3,2595 mM, the sensitivity of sensor is 2,0794 A. mM-1. mM-2.

Preparation and Characterization of Supported H3PW12O40 and Supported Cesium-Substituted Dodecatungstophosphate

2012 ◽  
Vol 509 ◽  
pp. 321-327 ◽  
Author(s):  
Zi Li Liu ◽  
Cui Xia Xu ◽  
Qian Wen Dai ◽  
Chao Xiang ◽  
Jian Jie Zhang
Keyword(s):  
Solid Acid ◽  
Solid Acid Catalysts ◽  
Incipient Wetness Impregnation ◽  
Acid Catalysts ◽  
X Ray Diffraction ◽  
X Ray ◽  
Highly Dispersed ◽  
Probe Experiment ◽  
Ft Ir

Supported H3PW12O40 (HPW) and supported Cesium-Substituted dodecatungsto-phosphate are eco-friendly solid acid catalysts. A series of different loading H3PW12O40/SiO2 and HPW/diatomite were prepared by a typical incipient wetness impregnation of methanol, meanwhile SiO2 and diatomite supported Cs-salt catalysts were prepared via two-step impregnating method. The catalysts were investigated by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The results indicate that the Keggin structure of HPW is intact in the SiO2-supported HPW and SiO2-supported CsHPW. HPW and CsHPW are highly dispersed in the SiO2 at the low loading, while the loading is more than 40% the catalyst grains increase and gather on the surface of the carrier. What's more, diatomite is not a suitable support. HPW and CsHPW have better distribution in the SiO2 than in the diatomite. The activity of catalyst was tested in probe experiment of the alkylation of thiopene (TH) with 1-hexene.

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