scholarly journals Facile Preparation of Phosphotungstic Acid-Impregnated Yeast Hybrid Microspheres and Their Photocatalytic Performance for Decolorization of Azo Dye

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Lan Chen ◽  
Bo Bai
Keyword(s):  
Phosphotungstic Acid ◽  
Uv Light ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Uniform Size ◽  
Xrd Pattern ◽  
Ft Ir ◽  
Red Dye ◽  
Yeast Hybrid

Phosphotungstic acid (HPW)-impregnated yeast hybrid microspheres were prepared by impregnation-adsorption technique through tuning pH of the aqueous yeast suspensions. The obtained products were characterized by field emission scanning electron microscopy (FE-SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), thermogravimetry-differential scanning calorimetry (TG-DSC), and ultraviolet-visible spectrophotometry (UV-Vis), respectively. FE-SEM and EDS ascertain that the HPW has been effectively introduced onto the surface of yeast, and the resulting samples retain ellipsoid shape, with the uniform size (length 4.5 ± 0.2 μm, width 3.0 ± 0.3 μm) and good monodispersion. XRD pattern indicates that the main crystal structure of as-synthesized HPW@yeast microsphere is Keggin structure. TG-DTA states that the HPW in composites has better thermal stability than pure HPW. Fourier transform infrared spectroscopy (FT-IR) elucidates that the functional groups or chemical bonds inherited from the pristine yeast cell were critical to the assembling of the composites. UV-Vis shows that the obtained samples have a good responding to UV light. The settling ability indicates that the hybrid microspheres possess an excellent suspension performance. In the test of catalytic activity, the HPW@yeast microsphere exhibits a high photocatalytic activity for the decoloration of Methylene blue and Congo red dye aqueous solutions, and there are a few activity losses after four cycles of uses.

Preparation and Characterization of Nanocrystalline La2Ti2O7 by Microwave Assisted Process

2016 ◽  
Vol 852 ◽  
pp. 525-529 ◽  
Author(s):  
Ying Zhou ◽  
Zhi Yong Mei ◽  
Hai Shao Ye ◽  
Wen Wen Su ◽  
Xi Zhao ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Uv Light ◽  
Raw Materials ◽  
Spherical Shape ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
Microwave Assisted ◽  
Average Grain Size ◽  
Ft Ir

Using La (NO3)3·6H2O, TiCl4 , and citric acid as the main raw materials, nanocrystalline La2Ti2O7 samples were prepared by microwave assisted method. The structure and morphology of samples were characterized by thermogravimetric and differential thermal analysis (TG-DTA), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier Transform Infrared (FT-IR) spectroscopy. The photocatalytic activity of La2Ti2O7 was studied for methyl orange (MO) used as simulated sewage. It was found that the single phase La2Ti2O7 could be obtained through the calcination of microwave processed La2Ti2O7 precursors at 600 °C. The resulted product had an approximate spherical shape and average grain size of 50 nm in diameter. Under UV light, the photocatalytic experiment indicated that the prepared La2Ti2O7 nanocrystalline had high photocatalytic activity for degradation of methyl orange.

scholarly journals Nematic Phase Induced from Symmetrical Supramolecular H-Bonded Systems Based on Flexible Acid Core

Crystals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 801 ◽  
Author(s):  
Hoda A. Ahmed ◽  
Muna S. Khushaim
Keyword(s):  
Uv Spectroscopy ◽  
X Ray Diffraction ◽  
Terminal Complex ◽  
Scanning Calorimetry ◽  
Xrd Pattern ◽  
X Ray ◽  
Smectic A ◽  
Ft Ir ◽  
Nematic Phases ◽  
Ft Ir Spectroscopy

New symmetrical 1:2 supramolecular H-bonded liquid crystals (SMHBLCs) interactions, A/2Bn, were formed between adipic acid and 4-(4′–pyridylazophenyl) 4″-alkoxybenzoates. Optical and mesomorphic behaviors of the prepared SMHBLC complexes were investigated using differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray diffraction (XRD). FT-IR spectroscopy was carried out to confirm the H-bond interactions of the prepared complexes via Fermi bands formation. Their photo-physical properties were investigated by UV-spectroscopy and the observed absorbance values were found to be mainly dependent on the length of the terminal alkoxy chain. Mesomorphic behaviour for all A/2Bn complexes revealed that all complexes are dimorphic-exhibiting enantiotropic mesophases with induced nematic phases, except for the long chain terminal complex which exhibits only a monomorphic smectic A phase. In order to investigate the effect of mesogenic core geometry on the mesophase properties, a comparison was established between the mesomeric behaviors of the present complexes and previously reported rigid core acid complexes. Finally, the XRD pattern confirmed the POM and DSC results.

scholarly journals Nematogenic Laterally Substituted Supramolecular H-Bonded Complexes Based on Flexible Core

Crystals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 878 ◽  
Author(s):  
H.A. Ahmed ◽  
Muna S. Khushaim
Keyword(s):  
Uv Spectroscopy ◽  
Supramolecular Complexes ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Xrd Pattern ◽  
X Ray ◽  
Ft Ir ◽  
Chain Lengths ◽  
Flexible Core ◽  
Ft Ir Spectroscopy

New laterally CH3-substituted series of 1:2 hydrogen-bonded supramolecular complexes (HBSMCs) based on flexible acid core were prepared and mesomorphically investigated. Mixtures were formed through H-bonded interactions between adipic acid (A) and 4-(2-(pyridin-4-yl)diazenyl-(3-methylphenyl) 4-alkoxybenzoate (Bn). Mesomorphic and optical properties were investigated by differential scanning calorimetry (DSC), polarized optical microscopy (POM), X-ray diffraction (XRD), and UV-spectroscopy. HBSMCs formed from 1:2 mol mixture of A:2Bn, where the base component (B) bearing different alkoxy chain lengths from n = 8 to 14. The new HBSMCs (A/2B) interactions were confirmed by Fermi-bands formation via FT-IR spectroscopy measurements. Results revealed that all prepared HBSMCs are enantiotropic, exhibiting induced nematic (N) phase. The XRD pattern confirmed the POM texture results. Moreover, a comparison was made between the new laterally HBSMC series based on flexible core and the previously analyzed laterally neat complexes.

Liquid crystalline polyureas with oligo(ethylene glycol) sequences

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Shahram Mehdipour-Ataei ◽  
Leila Akbarian-Feizi
Keyword(s):  
Liquid Crystalline ◽  
Spectroscopic Method ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Subsequent Reaction ◽  
Scanning Calorimetry ◽  
Polar Solvents ◽  
X Ray ◽  
H Nmr ◽  
Ft Ir

AbstractA diamine monomer containing ester, amide and ether functional groups was prepared and its polymerization reaction with different diisocyanates to give main chain poly(ester amide ether urea)s was investigated. The monomer was synthesized via reaction of terephthaloyl chloride with 4-hydroxybenzoic acid and subsequent reaction of the resulted diacid with 1,8-diamino-3,6-dioxaoctane. The polymers were characterized by FT-IR and 1H-NMR spectroscopic method and elemental analysis. The resulting polymers exhibited excellent solubility in polar solvents. Crystallinity of the resulted polymers was evaluated by wide-angle X-ray diffraction (WXRD) method, and they exhibited semi-crystalline patterns. The glass transition temperatures (Tg) of the polymers determined by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were in the range of 88-112 °C. The temperatures for 10% weight loss (T10) from their thermogravimetric analysis (TGA) curves were found to be in the range of 297-312 °C in air. Also the prepared polyureas showed liquid crystalline character.

Synthesis and Properties of Thermotropic Liquid Crystalline Polyesters with Flexible Polymethylene Spacer

2010 ◽  
Vol 428-429 ◽  
pp. 126-131
Author(s):  
Wei Zhong Lu ◽  
Chun Wei ◽  
Qui Shan Gao
Keyword(s):  
Optical Microscopy ◽  
Liquid Crystalline ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Structure Morphology ◽  
Temperature Ranges ◽  
Ft Ir ◽  
Diffraction Peaks ◽  
Ubbelohde Viscometer

Polymethylene bis(p-hydroxybenzoates) were prepared from methyl p-hydroxybenzoate and different diols by melted transesterification reaction. Three liquid crystalline polyesters were synthesized from terephthaloyl dichloride and polymethylene bis(p-hydroxybenzoates). Its structure, morphology and properties were characterized by Ubbelohde viscometer, Fourier transform infrared spectroscopy (FT-IR), Differential scanning calorimetry (DSC), polarized optical microscopy (POM) with a hot stage, and wide-angle X-ray diffraction (WAXD). Results indicated that the intrinsic viscosities were between 0.088 and 0.210 dL/g. Optical microscopy showed that the TLCP has a highly threaded liquid crystalline texture and a high birefringent schlieren texture character of nematic phase and has wider mesophase temperature ranges for all polyesters. DSC analysis were found that the melting point (Tm), isotropic temperature (Ti) of TLCPs decreased and the temperature range of the liquid crystalline phase became wider with increased number of methylene spacers in the polyester. The WAXD results showed that TLCPs owned two strong diffraction peaks at 2θ near 19° and 23°.

Study on Photocatalytic Properties of Anatase Phase TiO2 Synthesized by Ultrasonic-Assisted Hydrolysis

2012 ◽  
Vol 573-574 ◽  
pp. 110-114 ◽  
Author(s):  
Jin Xia ◽  
Ri Ya Jin ◽  
Kai Xuan Guo ◽  
Si Jing Yang
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Uv Light ◽  
Anatase Phase ◽  
Ultrasonic Method ◽  
X Ray Diffraction ◽  
Hydrolysis Method ◽  
Titanium Tetra Isopropoxide ◽  
Ultrasonic Assisted ◽  
Ft Ir

Titanium dioxide powders were synthesized by ultrasonic-assisted hydrolysis reaction of titanium tetra-isopropoxide at the low-temperature. The samples were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD). The photocatalytic activity of samples were investigated by the degradation of methyl orange under UV light radiation (6W, λ= 352nm) at room temperature. The results indicated that the products were mainly composed of high homogeneity anatase phases, and the methyl orange degradation rate can reach more than 90% under ultraviolet irradiation 180min. The photocatalytic activity of the samples prepared by ultrasonic method is higher than that of the samples prepared by conventional hydrolysis method.

scholarly journals Oxide-Clay Mineral as Photoactive Material for Dye Discoloration

Minerals ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 132
Author(s):  
Maicon O. Miranda ◽  
Bartolomeu Cruz Viana ◽  
Luzia Maria Honório ◽  
Pollyana Trigueiro ◽  
Maria Gardênnia Fonseca ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Clay Mineral ◽  
Uv Light ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Zirconium Oxides ◽  
Transmission Electron ◽  
Palygorskite Clay

Titanium and zirconium oxides (TiO2 and ZrO2, respectively) were obtained from alkoxides hydrolyses, and then deposited into palygorskite clay mineral (Pal) to obtain new materials for photocatalytic applications. The obtained materials were characterized by structural, morphological, and textural techniques. X-ray diffraction (XRD) results confirmed the characteristic peaks of oxides and clay transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images of the modified palygorskite with both oxides showed that the clay was successfully modified by the proposed method. The increase in the specific surface area of the clay occurred when TiO2 and ZrO2 were deposited on the surface. The photocatalytic activity of these materials was investigated using the Remazol Blue anion dye under UV light. The evaluated systems presented high photocatalytic activity, reaching approximately 98% of dye discoloration under light. Thus, TiO2–Pal and ZrO2–TiO2–Pal are promising clay mineral-based photocatalysts.

Research and Preparation of Silver Free Amorphous Active Brazing Alloy

2015 ◽  
Vol 817 ◽  
pp. 96-103
Author(s):  
Wei Ping Fang ◽  
Yao Yong Yi ◽  
Feng Mei Liu ◽  
Zheng Lin Liu ◽  
Zhen Hua Deng
Keyword(s):  
Bending Strength ◽  
Mechanical Test ◽  
Amorphous Material ◽  
Chemical Compositions ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Xrd Pattern ◽  
Spreading Area ◽  
Wetting Ability ◽  
Wetting Contact Angle

A silver free amorphous Cu-35Ti-12Ni active brazing alloy was successfully prepared in this work. The crystallinity, microstructure, and chemical composition were characterized with X-ray diffraction (XRD), scanning electron microscope (SEM), and energy-dispersive spectrometry (EDS), respectively. A typical characteristic peak of amorphous material was observed in the XRD pattern. The microstructures and chemical compositions of the silver free amorphous alloy were uniform. Differential scanning calorimetry (DSC) result shows that the amorphous silver free brazing alloy has higher melting temperature than commercial silver brazing alloy (Ag-26.5Cu-1.5Ti). Wetting contact angle and spreading area on Si3N4 ceramic substrate were used to evaluate the wetting ability of brazing alloy. The wetting angle was smaller than 5o, and the spreading area was 141.6 mm2 at 1100°C. The bending strength of silver free brazing alloy/Si3N4 was also carried out. The mechanical test shows that the amorphous Cu-35Ti-12Ni/Si3N4 has higher joint strength (304.7MPa) than the crystal Cu-35Ti-12Ni/Si3N4 (294.7MPa) at room temperature.

Compatibility between Magnesium Stearate and Pharmaceutical Acidic Active Compounds/Excipients with DSC

2020 ◽  
Vol 856 ◽  
pp. 190-197
Author(s):  
Pornsit Chaiya ◽  
Thawatchai Phaechamud
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnesium Stearate ◽  
X Ray Diffraction ◽  
Salt Form ◽  
Scanning Calorimetry ◽  
Powder Mixtures ◽  
X Ray ◽  
Pharmaceutical Excipients ◽  
Drug Compounds ◽  
Ft Ir

Compatibility investigation was performed between magnesium stearate and acidic drug compounds (ibuprofen, indomethacin and valproic acid) and acidic pharmaceutical excipients (lactic acid and citric acid) using differential scanning calorimetry (DSC). DSC study indicated the possible incompatibility for the mixture between magnesium stearate and any compounds. Alteration in DSC thermogram was found in all mixtures. The eutectic phenomenon was found in the powder mixture of magnesium stearate and ibuprofen. In addition, the presence of melting endothermic peak of stearic acid in other powder mixtures except the mixture of magnesium stearate and indomethacin indicating breakage of salt form of magnesium stearate. This alteration could relate to the influence on physicochemical properties of drug compounds and pharmaceutical excipients which powder x-ray diffraction (PXRD) and Fourier Transform Infrared Spectroscopy (FT-IR) should be further analyzed to confirm the interactions between compounds.

Stress-Induced Crystal-to-Crystal Transformations in High-Density Polyethylene-Layered Silicate Nanocomposites: A Spectroscopic Study

2005 ◽  
Vol 59 (9) ◽  
pp. 1148-1154 ◽  
Author(s):  
Spiros Tzavalas ◽  
Vasilis G. Gregoriou
Keyword(s):  
High Density Polyethylene ◽  
Mechanical Strain ◽  
Layered Silicate ◽  
High Density ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Polyethylene Matrix ◽  
Dsc Measurements ◽  
Infrared Measurements ◽  
Ft Ir

High-density polyethylene (HDPE)–clay nanocomposites have been prepared using the melt intercalation technique. Organically modified montmorillonite at various loadings (0.5–7%) was used as a nanoadditive. Fourier transform infrared spectroscopy (FT-IR) was utilized for the first time to monitor the stress-induced crystal-to-crystal transformations of the polyethylene matrix with respect to the clay loading as well as to the degree of mechanical strain. In addition, polarized infrared measurements revealed information on both the orientation and the stress-induced distortion of the crystals. It was concluded that the crystal-to-crystal transformations are hindered by the presence of the clay, which also prevented the crystals from orienting even at low clay loadings (1%). Finally, X-ray diffraction (XRD) and differential scanning calorimetry (DSC) measurements confirmed the presence of the stress-induced crystalline structures in agreement with the infrared measurements.

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