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Nanostructured CuO has been successfully synthesized via Thermal decomposition method at 700^∘C. Prepared CuO was characterized using IR spectra, X-ray diffraction (XRD) and scanning electron microscopy (SEM). IR spectra confirm the metal–oxygen bonding in these nanoparticles. The XRD pattern confirms a single-phase crystalline nature of the nanoparticles. The synthesized CuO was demonstrated as an efficient catalyst in degradation of Rhodamine B in the presence of light through oxidation. More than 93% of the Rhodamine B dye was degraded after 150min. It was observed that photocatalytic degradation of dyes follows pseudo-first-order kinetics. A tentative mechanism has also been proposed for the photocatalytic degradation of dyes in the presence of copper oxide semiconductor.

For exploring the interesting solvent effect on structure and morphology, a variety of MgWO₄ nanoparticles were prepared by a one-pot solvothermal method with different proportional solvents of water and ethylene glycol. The results showed that monoclinic wolframite crystalline structure of MgWO₄ was successfully synthesized, corresponding to two standard cards of MgWO₄ (JCPDS No. 27-0789) and MgWO₄ (JCPDS No. 19-0776), respectively. The morphology of MgWO₄ nanoparticles presents eight different shapes and orderly transforms from one shape to another with increasing water content in mixed EG-water solvents, and a possible mechanism was proposed. The catalytic activities of these MgWO₄ nanoparticles on the thermal decomposition of Ammonium Perchlorate (AP) were compared using differential scanning calorimetry (DSC) method, and found to present good change rule with particle size.

Ceria (CeO₂) nanoparticles (NPs) have been produced from cerium nitrate and walnut shell as a worthless agricultural waste by a thermal decomposition method followed by open air calcination. These NPs further were characterized using powder X-ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy, energy dispersive X-ray spectroscope and Fourier transform infrared spectroscopy. Moreover, particle sizes can be tuned by changing cerium source/biomass ratio. To test the catalytic activity of cerium NPs as a heterogeneous catalyst, we selected three-component synthesis of 3,4-dihydroquinoxalin-2-amine. Also, the efficiency of CeO₂ NPs as a support for palladium NPs and subsequent use in aerobic oxidation of alcohols has been investigated. TEM image of a recovered catalyst indicates the formation of 12 nm sized palladium NPs within the cerium oxide NPs. The catalyst is quite effective for the oxidation of primary and secondary benzylic alcohols into their corresponding aldehydes and ketones under atmospheric pressure of air. Oxidation of secondary aliphatic alcohols is performed in oxygen atmosphere.

This paper proposes a theoretical approach to predict the failure behavior of laminated carbon fiber reinforced polymer (CFRP) under combined thermal and mechanical loadings. Two types of CFRP Laminates, i.e., CCF300/BA9916 and T700/BA9916, are investigated, and TGA tests in both nitrogen and oxidation environments at different heating rates are carried out to obtain the thermal decomposition kinetic parameters of polymer matrix and carbon fiber. Based on the thermal decomposition behavior and a multi-level structure model, the thermal physical properties, mechanical properties and thermal deformations of the laminated composites at high temperatures are obtained. Then substituting thermally degraded properties into constitutive equations of composite materials as macroscopic defects, the damage mode and failure strength of the laminated composite under thermo-mechanical loadings is obtained. Predicted elastic properties and failure strength are compared with experimental results as well as previous models. Effects of heating rates and heating environments through rigorous physical model are considered in the present work. It is found that the heating rate significantly affects the thermal and mechanical properties, the higher the heating rate, the less degraded are the thermo-mechanical properties and failure strength at a given temperature. Young’s modulus and failure strength of T700/BA9916 are higher than those of CCF300/BA9916 at high temperatures, due to the higher volume fraction of carbon fibers, which are less weakened in thermal environment.

Three-dimensionally ordered macroporous (3DOM) CuO is prepared by colloidal crystal templated method. The obtained 3DOM structure with about 230nm pore diameter is composed of small CuO windows. The special structured CuO is used as a catalyst for thermal decomposition of ammonium perchlorate (AP) and its catalytic activity is measured by simultaneous thermogravimetry-differential scanning calorimetry (TG-DSC) techniques. Test results show that thermal decomposition performance is significantly improved after adding 2wt.% 3DOM CuO.

Alkyl methyl di(tri)thiocarbonates can be thermally decomposed into alkenes. In this paper, theoretical calculations were used to calculate the thermal decomposition procedures. Six compounds, including ethyl, isopropyl and $t\text{-}\mathrm{\text{butyl}}$ dithiocarbonate and trithiocarbonate, were examined. For each decomposition, nine possible paths were considered, including the paths leading to the desired alkene products, as well as rearrangement and elimination reactions. This calculation was performed with the MP2/6-31G(d) method. Wiberg bond indices were also calculated to further reveal the reaction progress.

This paper reports on the preparation of high purity ZnS nanoparticles by a facile single step solvent-free route via thermal decomposition of zinc acetate dihydrate and thiourea in air atmosphere. The third-order optical nonlinearity of the prepared ZnS nanoparticles were measured by Z-scan technique using continuous wave 532-nm diode pumped Nd:YAG laser. From nonlinear optical (NLO) measurements, the prepared ZnS nanoparticles possess negative nonlinearity i.e., self-defocusing. Open aperture Z-scan measurement shows saturable absorption within the medium. These results show that the prepared ZnS nanoparticles are promising candidate for various potential applications in the field of nonlinear optics.

The decomposition of goethite and goethite/siderite concentrates into hematite with thermal modification was studied through the measurements of X-ray diffraction (XRD), scanning electronic microscope (SEM) and thermal gravimetric analysis (TGA). The experimental results showed that goethite decomposed into hematite directly at around 300°C without any intermediate phase and the decomposition of siderite completed at 500°C. Nanoscale granular structures were observed in the thermally treated products. It deserves highlighting that the decomposition processes proceeded from surfaces into bulks.

A hot spot model, involving interaction of pulse laser with nanoparticles where heat diffusion and exothermic chemical reaction are considered and spread out of heat and chemical reaction, is developed to model the thermal reaction dynamic process of Al/NC (nitrocellulose) nanothermites excited by pulse laser for the purpose of verifying the experimental ablation criterion proposed recently and providing a microscopic insight into different physical pathways leading to ablation. In this model, the spatial position and conversion of matters taking place in chemical reactions are regarded as the functions of time, space, and temperature. An exact expression of power density absorbed by nanoparticles in matrix is incorporated to calculate the diameters of chemical reaction region. Calculation results justify experimental ablation criterion, and show that thermal decomposition mechanism predominates the nanosecond pulse-excited process before ablation but it is not suitable for the 100 ps regime which is qualitatively attributed to shock pressure. The effects of pulse duration and nanoparticle size on ablation threshold are examined.

Mn₃O₄ nanocrystals have been prepared using [bis(2-hydroxyacetophenato)manganese(II)] as precursor. Transmission electron microscopy analysis demonstrated nanocrystals Mn₃O₄ with an average diameter of about 20 nm. The structural study by X-ray diffraction indicates that these nanocrystals have pure tetragonal phase. The phase pure samples were characterized using X-ray Photoelectron Spectroscopy for Mn 2p level. The values of binding energies are consistent with the relative values reported in the literature.

The synthesis of two new methacrylates such as 2-[(cyclohexylideneamino)oxy]-2-oxoethyl methylacrylate (CHOEMA) and 2-[(cyclopentylideneamino)oxy]-2-oxoethyl methylacrylate (CPOEMA) are described. The monomers produced from the reaction of corresponding cyclohexanone O-(2-chloroacetyl) oxime and cyclopentanone O-(2-chloroacetyl) oxime with sodium methacrylate was polymerized in 1,4-dioxane solution at 65°C using AIBN as an initiator. The monomers and their polymers were characterized by IR, ¹H- and ¹³C-NMR spectroscopy. The glass transition temperature of the polymers was investigated by DSC and the apparent thermal decomposition activation energies (E_d) were calculated by Ozawa and multiple heating rate kinetics (MHRK) method using the Shimadzu TGA thermobalance. By using gel permeation chromatography, weight-average (M_w) and number-average (M_n) molecular weights and polydispersity indices of the polymers were determined. The antibacterial and antifungal effects of the monomers and polymers were also investigated on various bacteria and fungi. The photochemical properties of the polymers were investigated by UV and FTIR spectra.

In this paper, we report a simple yet powerful synthetic method for obtaining monodispersed silver nanoparticles by direct thermal decomposition of two materials — one is silver acetate as a source of the metal core and the other is myristic acid as a capping agent. The reaction was performed at 250°C, the boiling point of myristic acid, without additional solvent. The nucleation and growth of the particles were monitored by dynamic light scattering in order to optimize the reaction time. By this simple procedure, we could obtain uniformly sized Ag nanoparticles with the average diameter of 4.8 ± 0.1 nm. Although the particles were synthesized at high temperature, the ligand exchange between myristates and alkanethiolates can be achieved at room temperature. Significant characteristics of Ag nanoparticles attributed to localized surface plasmons were investigated.

Cu nanoparticles have been synthesized by thermal decomposition of Cu-oleate complex, which was prepared by the reaction with CuCl₂ and sodium oleate in water solution. The monodispersed Cu nanoparticles were produced by controlling temperature (290°C). TEM images of the nanoparticles showed two-dimensional assembly of particles with diameter of 16.2 ± 2.9 nm, demonstrating the uniformity of these nanoparticles. EDX spectrum and XRD peaks of the nanoparticles showed the highly crystalline nature of the Cu structures. The decomposition of Cu-oleate complex was analyzed with TGA and the crystallization of Cu nanoparticles was observed with XRD.

The thermal decomposition pathway and desorption of diethylamido of tetrakis(diethylamido)zirconium [TDEAZr, Zr(N(C₂H₅)₂)₄] on Si(100) were studied using temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). During TPD experiments, ethylethyleneimine (C₂H₅N=CHCH₃), diethylamine [NH(C₂H₅)₂], acetonitrile (CH₃CN), ethylene (C₂H₄) and hydrogen (H₂) desorbed as the main decomposition products of diethylamido, which was chemisorbed on Si(100) through the scission of the zirconium–diethylamido bond in TDEAZr. After TPD runs, the formation of silicon carbide and silicon nitride was observed on the surface by XPS, indicating that a complete decomposition of diethylamido proceeded. This could be a reaction pathway of C, N incorporation in the thin film growth using TDEAZr as a Zr precursor.