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  • Author or Editor: Z. Yang x
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Abstract  

External-beam PIXE was used for the non-destructive analysis of early glasses unearthed from the tombs of Warring States (475–221BC) and Han Dynasty (BC 206–AD 220) in south China. It was found that these glasses were basically attributed to PbO—BaO—SiO2 system and K2O—SiO2 system. The results from the cluster analysis showed that some glasses had exactly the same recipe. The source of the K2O flux and the correlation between PbO and BaO are discussed. Some archeological information is revealed.

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Abstract  

Although Ir anomaly has been discovered in a number of C/T boundaries in the world, no positive results of this anomaly in Permian/Triassic (P/Tr) boundary were given. There are many well-developed P/T sections in South China. One of representative sections is located at the Baoqing quarry, Meishan Town, Changxin County, Zhejiang Province. Ir, Os, Re, Au, Pt, Cu and Mo were determined by the radiochemical procedure developed in our laboratory. (1) Besides those accessible by INAA. The results reveal that the refractory siderophile and other chalcophile elements have certain enrichment near and at the boundary layer. However, the Ir/Au and other element abundance ratios fail to accord with the extraterrestrial values. The nature of the boundary event was discussed in terms of elemental geochemistry.

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Abstract  

The concentrations of 14 elements, including Ir, Au, Co, Cr, Fe, Sr, Rb, K, Ta, Zn, Sb, Ba, Sc and Se, in the Wuxi fallen ice were determined by neutron activation analysis. The experimental results show that the relative concentration ratios of Ir/Co, Ir/Cr and Ir/Sc etc. in the ice water (0.0069, 0.00024 and 0.11, respectively) are quite close to those of Type C1 chondrite (0.0102, 0.00021 and 0.092, respectively), which implies that the fallen ice might be a piece of extraterrestrial substance.

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Abstract  

The crystal C81H78N12O6Cd3 was synthesized and its structure was determined by single crystal X-ray diffraction method. The complex crystallizes in the monoclinic system space group P21/n with cell parameters, a=15.959(4) , b=26.222(3) , c=25.907(6) , β=101.60(2). The non-isothermal kinetics of the crystal was studied by use of non-isothermal TG and DTG curves. The kinetic parameters were analyzed by means of integral and differential methods, and mechanism functions of the thermal decomposition reaction for its second step were proposed. The kinetic equation of thermal decomposition is expressed as: dα/dt=Aexp(-E/RT)1.5(1-α)4/3[1/(1-α)1/3-1]−1. The average values of E(kJ mol−1) and lnA/s−1 are 339.25, 43.95, respectively.

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Abstract  

The effects of cisplatin and its trans isomer transplatin on the thermal denaturation of G-actin were studied with a Micro DSC-III differential scanning calorimeter. The denaturation enthalpy of G-actin was found to be 12 J g–1, and the denaturation temperature was 328 K. The thermal denaturation curve showed that increasing cisplatin concentration decreased the enthalpy change. However, after the ratio of cisplatin to G-actin attained 8:1 (mol:mol), the denaturation enthalpy no longer decreased. Transplatin decreased the enthalpy change more rapidly. In contrast with cisplatin, the denaturation peak at 328 K disappeared, and a strong exothermic peak appeared at 341 K when the ratio of transplatin to G-actin was 8:1 (mol:mol). The enthalpy change was 75 J g–1, which is far in excess of the range of weak interactions. This strong exothermic phenomenon probably reflects the agglutination of protein. The effects of cisplatin and transplatin on the number of the free thiol groups of G-actin are discussed.

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Abstract  

The effects of Amoxicillin Sodium and Cefuroxime Sodium on the growth of E. coli DH5α were investigated by microcalorimetry. The metabolic power-time curves of E. coli DH5α growth were determined by using a TAM air isothermal microcalorimeter at 37�C. By evaluation of the obtained parameters, such as growth rate constants (k), inhibitory ratio (I), the maximum heat power (P m) and the time of the maximum heat power (t m), one found that the inhibitory activity of Amoxicillin Sodium vs. E. coli DH5α is enhanced with the increasing of the Amoxicillin Sodium concentration, and the Cefuroxime Sodium has a stimulatory effect on the E. coli DH5α growth when the concentration is about 1 μg mL−1. The IC50 for the Amoxicillin Sodium and the Cefuroxime Sodium are 1.6 and 2.0 μg mL−1, respectively, it implicates that the E. coli DH5α is more sensitive to Amoxicillin Sodium than Cefuroxime Sodium.

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Abstract  

A series of PA-TD mixtures were prepared and their thermal properties were studied by DSC and thermal conductivity measurement. The phase diagram of the binary system was constructed, which showed an eutectic behavior for the solid-liquid equilibrium line. The eutectic composition of the binary system was at the mass fraction of TD near 0.7 with an eutectic temperature of about 29°C. At TD side, PA was partially miscible in the TD solid matrix and the solid phase transition of TD had an effect on the solidus line. The eutectic composition mixture could be viewed as a new phase change material with large thermal energy storage capacity.

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Abstract  

The effects of multi-walled carbon nanotubes (MWNTs) on the phase change enthalpy (ΔH) and the thermal conductivity (κ) of a solid-liquid phase change materials (PCM), palmitic acid (PA), have been investigated. The results showed that both the ΔH and the κ of the composite were lower than that of PA when the loading of MWNTs was small. As the concentration of MWNTs in the composites increased, the ΔH of the composites was slightly improved and then decreased linearly. However, the κ of the composites was monotonously increased from the minimum value. When the loading of MWNTs increased to 5% and no surfactant was added, the κ of the composite was enhanced to be 26% higher than that of PA. The κ of the composite could be enhanced by CTAB instead of SDBS when the loading of MWNTs was small, as SDBS showed no obvious effect on the κ of the composites. Furthermore, the effects of surface modification of MWNTs on the ΔH and the κ of the composites have also been investigated.

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Abstract  

The thermal decomposition of strontium acetate hemihydrate has been studied by TG-DTA/DSC and TG coupled with Fourier transform infrared spectroscopy (FTIR) under non-isothermal conditions in nitrogen gas from ambient temperature to 600°C. The TG-DTA/DSC experiments indicate the decomposition goes mainly through two steps: the dehydration and the subsequent decomposition of anhydrous strontium acetate into strontium carbonate. TG-FTIR analysis of the evolved products from the non-oxidative thermal degradation indicates mainly the release of water, acetone and carbon dioxide. The model-free isoconversional methods are employed to calculate the E a of both steps at different conversion α from 0.1 to 0.9 with increment of 0.05. The relative constant apparent E a values during dehydration (0.5<α<0.9) of strontium acetate hemihydrate and decomposition of anhydrous strontium acetate (0.5<α<0.9) suggest that the simplex reactions involved in the corresponding thermal events. The most probable kinetic models during dehydration and decomposition have been estimated by means of the master plots method.

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Abstract  

The uranium(VI) accumulation was studied in detail by using the biomass of mangrove endophytic fungus Fusarium sp.#ZZF51 from the South China Sea. The uranium(VI) biosorption process onto the tested fungus powders was optimized at pH 4.0, adsorption time 60 min, and uranium(VI) initial concentration 50 mg L−1 with 61.89% of removal efficiency. According to Fourier transform infrared spectra for the tested fungus before and after loaded with uranium(VI), the results showed that both of hydroxyl and carboxyl groups acted as the important roles in the adsorption process. In addition, the experimental data were analyzed by using parameter and kinetic models, and it was obtained that the Langmuir isotherm model and the pseudo-second-order kinetic model provided better correlation with the experimental data for adsorption of uranium(VI).

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