Microstructural characterization and mechanical properties of(TiC+TiB)/TA15 composites prepared by an in-situ synthesis method

Titanium matrix composites reinforced with ceramic particles are considered a promising engineering material due to their combination of high specific strength,low density,and high modulus.In this study,the TA15-based composites reinforced with a volume fraction of 10% to 25%(TiB+TiC)were prepared using powder metallurgy and casting technique.Microstructural characterization and phase constitution were examined using optical microscopy(OM),scanning electron microscopy(SEM),and X-ray diffraction(XRD).In addition,the microhardness,room temperature(RT)and high temperature(HT)tensile properties of the composites were evaluated.Results revealed that the reinforcements are distributed uniformly even in the composites with a high volume of TiB and TiC.However,as the volume fraction exceeds 15%,TiB and TiC particles become coarsening and exhibit rod-like and dendritic-like morphology.Microhardness increases gradually from 321.2 HV for the base alloy to a maximum of 473.3 HV as the reinforcement increases to 25vol.%.Tensile test results indicate that a reinforcement volume fraction above 20% is beneficial for enhancing tensile strength and yield strength at high temperatures,but it has an adverse effect on room temperature elongation.Conversely,if the reinforcement volume fraction is below 20%,it can improve high-temperature elongation when the temperature exceeds 600℃.

Synthesis, Characterization and Optical Morphology of ZnO Nanoparticles

The ZnO molecule plays an important role in the industry due to it special features, anti-corrosion anti-bacterial properties, as well as due to its low electrical conductivity and heat resistance. In these experimental researches, the sol-gel method was chosen, which enables control of nucleation, aging and growth of particles in the solution. ZnO synthesis was prepared utilizing chemical method with Zinc acetate dyhidrate and NaOH with the appropriate methanol solvent and heating (60˚C). The methods used in identification and characterization are FTIR, UV/VIS, OPTICAL MICROSCOPY, SEM and XRD. The FTIR spectra of synthesized ZnO with corresponding ones show characteristic bands at the corresponding wavelengths, which confirm the presence of ZnO nanoparticles. SEM characterization of ZnO shows the morphology of needle-shaped nanoparticles. XRD spectar in this research by chemical method indicates the particle size of 17.76 nm.

Recent advances in quantum dot catalysts for hydrogen evolution:Synthesis,characterization,and photocatalytic application

Photocatalytic water splitting is beneficial for the effective mitigation of global energy and environmental crises.Owing to multi-exciton generation,impressive light harvesting,and excellent photochemical properties,the quantum dot(QD)-based catalysts reveal a considerable potential in photocatalytic hydrogen(H_(2))production compared with bulk competitors.In this review,we summarize the recent advances in QDs for photocatalytic H_(2) production by enumerating different synthetic and characterization strategies for QDs.Various QDs-based photocatalysts are introduced and summarized in categories,and the role of different QDs in varied systems,as well as the mechanism and key factors that enhance the photocatalytic H_(2) generation performance,is discussed.Finally,conclusions and future perspectives in the exploration of highly efficient QDs-based photocatalysts for innovative applications are highlighted.

Synthesis, performance and structure characterization of glyoxal-monomethylolurea-melamine (G-MMU-M) co-condensed resin

In order to reduce the formaldehyde emission of formaldehyde-based wood adhesive from the source,it is aimed to develop a novel co-condensed resin of glyoxal-monomethylolurea-melamine(G-MMU-M).A series of G-MMU-M resins with various formulations of raw materials were successfully prepared.The basic properties and bonding performance of the G-MMU-M resins were determined.Furthermore,the structures of resins were characterized by FTIR,^(13)C NMR,XPS,and ESI-MS.The results show that the prepared G-MMU-M resin remains stable for 30 d,meanwhile,the dry and wet bonding strength of the plywoods bonded with the resins,solid content and viscosity are influenced greatly by the addition amount of melamine and MMU/G molar ratio.The G-MMU-M resins with MMU/G molar ratio of 0.9:1.0 and 8% melamine exhibit the highest dry and bonding strength of 1.98 MPa and 1.27 MPa,increased by 34% and 63%,respectively,in comparison with glyoxal-monomethylolurea(G-MMU)resin.In the G-MMU-M resins,there were four main oligomers including M—CH(—^(+)CH-MMU)-O-MMU,M-CH(—CH_(2)OH)-MMU-O-MMU,M—CH(—OH)—^(+)CH-MMU-O-MMU,and M—CH(—^(+)CH-MMU)-MMU-p-G.

Synthesis,Characterization of NaA Zeolite from Blast Furnace Slag(BFS)via Alkaline Fusion and Hydrothermal Treatment

A blast furnace slag zeolite(BFSZ)material was successfully synthesized from BFS by alkaline fusion and hydrothermal treatment.Via the analyses of XRD,FT-IR,FE-SEM,XRF,CEC and BET surface area measurement,when zeolite was synthesized at a crystallization temperature of 100℃with initial Si/Al ratio of 1:1,the main composition in the product is Na-A zeolite.Under the above conditions,the BFSZ was synthesized with CEC of 3.06 meq/g and maximum BET surface area of 37.55 m^(2)·g^(-1).Moreover,the incorporating of BFS-derived minor metals(such as Mg,Fe,and Ca)are found to be of little importance for the synthesis of BFSZ.Thus the obtained BFSZ material has a great adsorption performance for removing Mn^(2+),Cu^(2+),and NH_(4)^(+)ions diluted in water,owing to the higher CEC.

Synthesis and Characterization of 9,9-diethyl-1-phenyl-1,9-dihydrofluoreno[2,3-d]imidazole-ended Fluorophores

A series ofπ-conjugated compounds ending with 9,9-diethyl-1-phenyl-1,9-dihydrofluoreno[2,3-d]imidazole were conveniently synthesized by condensation of the key intermediate9,9-diethyl-N^(2)-phenyl-9H-fluorene-2,3-diamine with the corresponding symmetric aryl phthalaldehydes under very mild conditions.The structures of these compounds were confirmed by^(1)H NMR,^(13)C NMR,and HRMS.Their UV-Vis spectroscopy data,fluorescent spectroscopy data,and further details of the electronic properties from cyclic voltammetry measurements and theoretical calculations were studied.Most compounds possess good fluorescence-emitting ability with quantum yield of fluorescence values in the region of 0.36-0.92 and display emission within 449-513 nm depending on the molecular nature.

Solriamfetol impurities:Synthesis,characterization,and analytical method(UPLC-UV)validation

Given that impurities may affect the quality and safety of drug products,impurity identification and profiling is an integral part of drug quality control and is particularly important for newly developed medications such as solriamfetol,which is used to treat excessive daytime sleepiness.Although the highperformance liquid chromatography analysis of commercial solriamfetol has revealed the presence of several impurities,their synthesis,structure elucidation,and chromatographic determination have not been reported yet.To bridge this gap,we herein identified,synthesized,and isolated eight processrelated solriamfetol impurities,characterized them using spectroscopic and chromatographic techniques,and proposed plausible mechanisms of their formation.Moreover,we developed and validated a prompt impurity analysis method based on ultrahigh-performance liquid chromatography with UV detection,revealing that its selectivity,linearity,accuracy,precision,and quantitation limit meet the acceptance criteria of method validation stipulated by the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use.Thus,the developed method was concluded to be suitable for the routine analysis of solriamfetol substances.

Synthesis,Characterization and Impedance Analysis of Calcium-Doped Zinc Oxide Nanoparticles

The calcium-doped ZnO nanoparticles,Zn1-xCaxO(x=0,0.025,0.05,0.075)were prepared by the solution combustion meth­od.The synthesized nanoparticles were characterized by various techniques such as XRD,FTIR,Raman,FESEM-EDX,PL,Impedance,and UV-Vis.The Rietveld refinement of the X-ray diffractogram yields the crystalline structure and lattice parameters.Also,the XRD analysis shows that the substitution of Ca into ZnO does not alter the Wurtzite structure of ZnO.The crystallite size of the samples,calculated using the Scherer equation,was found to be between 46 nm and 92 nm.FTIR spectra detect the ZnO-re­lated vibration modes of the samples.The FESEM morphological images suggest the spherical shape of the synthesized nanopar­ticles.The EDAX spectra identify the presence of Zn,Ca,and O atoms in the samples.The Raman active modes of the ZnO phase were identified by Raman spectral analysis.The analysis of Photoluminescence(PL)spectra gives information about the UV emis­sion and other visible bands corresponding to violet,blue,and green emission representing different intrinsic defects in synthesized nanoparticles.Using UV-vis spectroscopy,the optical transparency and band gap values were examined.The energy band gap ob­tained by Tauc’s plot was decreased with the increase in Ca doping.Impedance analysis shows that the grain conductivity increased with the increase in dopant concentration.Contrarily,the total conductivity decreased with the increasing doping concentration due to increased grain boundary resistance.The proposed work demonstrates the changes in microstructure,electrical conductivity,and optical bandgap energy with Ca-doping.These synthesized Ca-doped ZnO nanoparticles could be promising materials for photo­catalytic applications.

Synthesis and Characterization of Microcapsules with Chlorpyrifos Cores and Polyurea Walls

Microcapsules with chlorpyrifos cores and polyurea walls were synthesized with 2,4-tolylene diisocyanate as an oil-soluble monomer and ethylenediamine as a water-soluble monomer via an interracial polycondensation reaction. The products were characterized by means of Fourier transform infrared spectrometry, ^13C NMR spectrometry and ^31p NMR spectrometry. The morphology, the particle size and the particle size distribution, and the thermal properties were also evaluated. The prepared microcapsules exhibit clear and smooth surfaces and have a mean diameter of 28. 13 μm. These microcapsules also have a good thermal stability for long-term use, and have potential applications in minimizing the toxicity of chlorpyrifos through controlled release.

Synthesis,characterization and catalytic properties of Y-β zeolite composites

Y-β zeolite composites were hydrotherrnally synthesized by using high silica Y zeolite as the precursor and characterized by XRD, N2 adsorption, SEM and IR spectra of pyridine. The result showed that the N2 adsorption-desorption isotherm of the zeolite composites had a distinct hysteresis loop, and the SEM result showed that the zeolite composites had a different morphology from Y, β and the corresponding physical zeolite mixture. The acid catalytic performance of the zeolite composite catalysts was investigated in the hydrocracking and hydroisomerization of n-octane, and the results showed that the composite materials exhibited an excellent hydrocracking activity and good hydroisomerization performance. The yield of i-C4 over the zeolite composite catalyst was 4.45% higher than that on the corresponding zeolite mixture in the n-octane hydrocracking process at 553 K. The isomerization ability of n-octane over the composite catalyst was 3.6 fold that of the corresponding mixture at 503 K.

Synthesis and Characterization of Quaternary Complexes Ln(CH_2ClCOO)_2 (NO_3) (phen)

Many trinary lanthanide complexes have been studied. However, few mixed anion complexes with bidentate heterocyclic amines were synthesized. We synthesized mixed anion complexes Ln ( CHi CICO0 )2 (NO3) (phen) which was determined by elemental analyses. The IR spectra analyses indicate that NO3 ,CH2 C1CO0- and phen are coordinated with Ln. The molar conductances of the complexes at 10-3 mol. L-1 were founded to be between 32.4 and 35.8 S. cma@mol- 1 , suggesting the nonelectrolytes in N Dimethylformamide. And we determined the fluorescent spectra Eu(CH2C1COO)2(NO3) ( phen ) and ESR spectra of Gd( CH2 ClC00 )2 ( NOs ) ( phen ) .

Synthesis and Characterization of Dual Acidic Ionic Liquids

Novel ionic liquids with dual acidity, of which the cation contains Brφnsted acidity and anions contain Lewis acidity were synthesized. These ionic liquids obtained were identified by NMR, FF-IR, SDT and FAB-MS. Their acidities were determined by pyridine probe on IR spectrography.

Synthesis and Characterization of Y-Doped Mesoporous CeO_2 Using A Chemical Precipitation Method

Using cetyltrimethylammonium bromide （CTAB） as the template agent, cerium nitrate as the cerium resource, yttrium nitrate as the yttrium resource, and ammonium carbonate as the precipitating agent, mesoporous CeO2 powders doped with different yttrium contents were successfully synthesized using a chemical precipitation method, under an alkalescent condition. Properties of the obtained samples were characterized and analyzed with X-ray diffraction （XRD）, energy dispersive analysis of X-rays （EDAX）, transmission electron microscopy （TEM）, infrared （IR） absorbance, and the BET method. For the prepared samples with 20% （molar ratio） Y-doped content, a BET specific surface area of 106. 6 m^2 · g^- 1, with an average pore size of3~27 nm were obtained. XRD patterns showed that the doped samples were with a cubic fluorite structure. TEM micrographs revealed that the doped samples showed a spherical morphology with a diameter ranging from 20 to 30 nm and a round pore shape. IR results indicated that the Ce-O-Ce vibration intensity decreased as the Y-doped content increased. N2 adsorption-desorption isotherms showed that the samples possessed typical mesopore characteristics. The average pore size of the samples decreased alter mesoporous CeO2 was doped with yttrium, and the average pore size decreased largely as the Y-doped content increased.

Synthesis and Characterization of CdSe Nanocrystals Capped by CdS

CdSe semiconductor nanocrystals capped by CdS were synthesized in the aqueous solution with 2 mercaptoethanol as the stabilizer. The CdS capping with a higher band gap than that of the core crystallite has successfully eliminated the surface traps. Optical absorption and fluorescence emission spectra were used to probe the effect of CdS passivation on the electronic structure of the nanocrystals. The composite CdSe/CdS nanocrystals exhibit strong, narrow(FWHM≤40 nm) and stable band edge photoluminescence. X ray powder diffraction, transmission electron microscopy and X ray photoelectron spectroscopy were used to analyze the composite nanocrystals and determine their average size, size distribution, shape, internal structure and elemental composition.

Preliminary Synthesis and Characterization of Mesoporous Nanocrystalline Zirconia

A novel method to prepare mesoporous nano-zirconia was developed. Thesynthesis was carried out in the presence of PEO surfactants via a solid-state reaction. Thematerials exhibit a strong diffraction peak at low 2θ angle and their nitrogenadsorption/desorption isotherms are typical of type IV with H1 hysteresis loops. The pore structureimaged by TEM can be described as wormhole domains. The tetragonal zirconia nanocrystals are uniformin size (around 1.5 nm) and their mesopores focus on around 4.6 nm. The zirconia nanocrystal growthis tentatively postulated to be the result of an aggregation mechanism. This study also revealsthat the PEO surfactants can interact with the Zr-O-Zr framework to reinforce the thermal stabilityof zirconia. The ratio of NaOH to ZrOCl_2, crystallization and calcination temperature play animportant role in the synthesis of mesoporous nano-zirconia.

Synthesis, Characterization and Antioxidative Activity of Lanthanide Complexes with Genistein

Six genistein lanthanide complexes, LnL_2 (OAc)·nH_2O [Ln=La(Ⅲ), Sm(Ⅲ), Eu(Ⅲ), Gd(Ⅲ), (Tb(Ⅲ),) Dy(Ⅲ); L=genistein; n=4, 7, 8] were synthesized and characterized on the basis of elemental analyses, IR, (()~1H) NMR spectra and molar conductivity. The scavenging activity of genistein and five lanthanides complexes on the hydroxyl free radicals (OH·) was also investigated by spectrophotometric methods. The results show that the scavenging activity of the complexes is better than that of the ligand and their scavenging ability can be assembled in the following order: Sm>La>Dy>Eu>Tb>L.

Synthesis, Characterization and Formation Mechanism of Friedel's Salt(FS:3CaO·A1_2O_3·CaCl_2·10H_2O) by the Reaction of Calcium Chloride with Sodium Aluminate

The synthesis of Friedel＇s salt （FS： 3CaO·Al2O3·CaCl2·10H2O） by the reaction of calcium chloride with sodium aluminate was investigated. Factors affecting the preparation of Friedel＇s salt, such as reaction temperature, initial concentration, titration speed, aging time and molar Ca/Al ratio were studied in detail. XRD, SEM images and particle size distribution show that the reaction temperature, aging time and molar Ca/Al ratio have significant effect on the composition, crystal morphology, and average particle size of the obtained samples. In addition, the initial CaCl2 concentration and NaAlO2 titration speed do not significantly influence the morphology and particle size distribution of Friedel＇s salt. With the optimization of the operating conditions, the crystals can grow up to a average size of about 28 μm, showing flat hexagonal （or pseudo- hexagonal） crystal morphology. Moreover, two potential mechanisms of Friedel＇s salt formation including adsorption mechanism and anion-exchange mechanism were discussed. In the adsorption mechanism, Friedel＇s salt forms due to the adsorption of the bulk C1- ions present in the solution into the interlayers of the principal layers, [Ca2Al（OH-）6·2H2O]＋, in order to balance the charge. In the anion-exchange mechanism, the freechloride ions bind with the AFro （a family of hydrated compounds found in cement） hydrates to form Friedel＇s salt by anion-exchange with the ions present in the interlayers of the principal layer, [Ca2Al（OH-）6. 2H2O]＋- OH-.

Synthesis, Characterization and Thermal Decomposition Mechanism of Cetyltrimethyl Ammonium Tetrathiotungstate

The synthesis, characterization and thermal decomposition mechanism of cetyltrimethyl ammonium tetrathiotungstate （CTriMATT） were studied herein. The as-synthesized CTriMATT was characterized by Elemental analysis, X-ray diffraction （XRD）, Fourier transform infrared （FT-IR）, Ultraviolet visible （UV-Vis） spectra. The results showed that the as-synthesized CTriMATT had high purity and good crystallinity. The introduction of alkyl groups induced a shift of the stretching vibration band of W-S bond to lower wavenumber, while it had no influence on the position of WS4^2-. Thermogravimetric analysis （TG）, differential thermal analysis （DTA） and in situ XRD characterizations revealed that CTriMATT began to decompose at 423 K in nitrogen and was converted to WS2 eventually. In addition, the decomposition product of CTriMATT at 673 K in nitrogen was characterized by N2 adsorption （BET） and scanning electron microscopy （SEM）. The results demonstrated that WS2 with higher specific surface area, and pore volume could be obtained from the thermal decomposition of CTriMATT in nitrogen.

Synthesis and structure characterization of diethyldiallylammonium chloride

The unsaturated quaternary ammonium salt diethyldiallylammonium chloride(DEDAAC) was synthesized in a two-step synthetic method. The influences of the adding method of raw materials and temperature on the yields of diethylallylamine (DEAA), and drying and temperature on the synthesis of DEDAAC were investigated. The content of in-process product DEAA was determined by non-aqueous titration. The structure of product DEDAAC was identified with IR, 1 H NMR and elemental analysis. The results show that adding allyl chloride and sodium hydroxide alternately can increase the yield of DEAA and decrease by-products. In further synthesizing of DEDAAC from DEAA, the step of drying DEAA is very necessary. When DEAA is dried by solid sodium hydroxide, good columnar crystals with a high purity(mp 199.5-201.0 ℃) are obtained; when DEAA is undried or the content of water in DEAA is above 20%, only platelets with bad quality are obtained even without crystals. The suitable synthesis conditions for DEAA and DEDAAC are 35 ℃, 6 h and 40 ℃, 36 h, respectively, and their yields are 69.7% and 67.3%, respectively.

Synthesis and Characterization of Montmorillonite Inorgano-Intercalation Compound Assisted by Microwave Irradiation

A montmorillonite inorgano-intercalation compound（MIIC） was synthesized by using a purified Na-exchanged bentonite（PNaB） as a matrix and Al-pillaring ion as an intercalating reagent under microwave irradiation.The synthesized products were characterized by X-ray diffraction（XRD）,^27Al magic angle sample-spinning nuclear magnetic resonance（^27Al MAS NMR）,specific surface area（BET） measurement,and adsorption density determination.The results show that,at 5% solid（PNaB） concentration and 7 minutes irradiation in a 130 W microwave oven,the basal spacing d（001） of the synthesized MIIC increases to 1.740 nm from the original 1.218 nm of PNaB.The MIIC has much higher adsorptive densities to F-and Cr^6＋ from aqueous solution than the PNaB.The adsorption isotherm of F-on the MIIC follows the Freundlich equation,and the increased adsorption is mainly due to the porous structure of the MIIC which created larger adsorption surfaces.The adsorption isotherm of Cr^6＋ on MIIC follows the Langmuir equation and the adsorption is mainly monolayer as a result of chemisorptions.