Authors:B. Hu, Y. Song, L. Wang, Q. Zhang, J. Li, K. Wei, Y. Chen, and L. Zhang
Electronic stopping power of 19F in Ni, Pd and Gd was measured and compared to Mstar and SRIM calculation as well as experimental results published in literature.
It turns out that the present electronic stopping power agrees reasonably well with them.
Authors:J. Wang, M. Wu, B. Bao, Zh. Li, Q. Wang, X. Zhang, and G. Ye
This paper reports the study of hydrogen and carbon monoxide produced by radiation degradation of N, N-dimethylhydroxylamine
(DMHA). The results show that when the concentration of DMHA is between 0.1M–0.5M and the dose is between 10–1000 kGy, the
volume fraction of hydrogen is very high and increases with the dose. The volume fraction of hydrogen is little dependent
on the concentration of DMHA at lower dose but increases with increasing concentration of DMHA at higher dose. The volume
fraction of carbon monoxide is very low.
Authors:B. Tong, Z. Tan, X. Lv, L. Sun, F. Xu, Q. Shi, and Y. Li
The molar heat capacities Cp,m of 2,2-dimethyl-1,3-propanediol were measured in the temperature range from 78 to 410 K by means of a small sample automated
adiabatic calorimeter. A solid-solid and a solid-liquid phase transitions were found at T-314.304 and 402.402 K, respectively, from the experimental Cp-T curve. The molar enthalpies and entropies of these transitions were determined to be 14.78 kJ mol−1, 47.01 J K−1 mol− for the solid-solid transition and 7.518 kJ mol−1, 18.68 J K−1 mol−1 for the solid-liquid transition, respectively. The dependence of heat capacity on the temperature was fitted to the following
polynomial equations with least square method. In the temperature range of 80 to 310 K, Cp,m/(J K−1 mol−1)=117.72+58.8022x+3.0964x2+6.87363x3−13.922x4+9.8889x5+16.195x6; x=[(T/K)−195]/115. In the temperature range of 325 to 395 K, Cp,m/(J K−1 mol−1)=290.74+22.767x−0.6247x2−0.8716x3−4.0159x4−0.2878x5+1.7244x6; x=[(T/K)−360]/35. The thermodynamic functions HT−H298.15 and ST−S298.15, were derived from the heat capacity data in the temperature range of 80 to 410 K with an interval of 5 K. The thermostability
of the compound was further tested by DSC and TG measurements. The results were in agreement with those obtained by adiabatic
Authors:J.-J. Zhang, R.-F. Wang, J.-B. Li, H.-M. Liu, and H.-F. Yang
The thermal decomposition of Eu2(BA)6(bipy)2 (BA=C2H5N–2, benzoate; bipy=C10H8N2, 2,2'-bipyridine)and its kinetics were studied under the non-isothermal condition by TG-DTG, IR and SEM methods. The kinetic
parameters were obtained from analysis of the TG-DTG curves by the Achar method, the Madhusudanan-Krishnan-Ninan (MKN) method,
the Ozawa method and the Kissinger method. The most probable mechanism function was suggested by comparing the kinetic parameters.
The kinetic equation for the first stage can be expressed as: dα/dt=Aexp(–E/RT)3(1–α)2/3.
Authors:M. Lu, B. Wang, Zh. Li, Y. Fei, L. Wei, and Sh. Gao
Antifreeze protein (AFP) can lower the freezing point by inhibiting the growth of ice crystals. In this article, the thermal
hysteresis activity (THA) of a plant AFP was measured with differential scanning calorimetry (DSC). As is shown, when the
amount of ice in the sample was less than 5% THA of this AFP reached as high as 0.35°C. The secondary structure of this AFP
was studied with circular dichroism (CD). The CD spectrum from 195to 240 nm indicated a well-defined secondary structure consisting
11% α-helix, 34%antiparallel β-sheet and 55% random coil.
Authors:J. Xing, Z. Tan, Q. Shi, B. Tong, S. Wang, and Y. Li
The low-temperature heat capacities of 1-hexadecanol have been measured with an automatic adiabatic calorimeter over the temperature
range from 80 to 370 K. A solid-liquid phase transition was observed at Tm=322.225±0.002 K and the molar enthalpy and entropy of fusion were determined to be 57.743±0.008 kJ mol−1 and 179.19±0.04 J K−1 mol−1, respectively. The purity, the real melting point (T1) and the ideal melting point without any impurity or absolutely purity (T0) of the sample under investigation were determined to be 99.162 mol%, 322.21 and 322.34 K, respectively, by fractional melting
method. According to the polynomial equation of heat capacity and thermodynamic relationship, the thermodynamic functions
of the compound relative to the reference temperature 298.15 K were calculated in the temperature ranges of 80 to 370 K with
an interval of 5 K. In addition, further researches of thermal properties for this compound were carried out by means of TG/DTG.
Authors:J. Tian, S. Han, H. Zeng, B. Wang, Z. Li, and Y. Zhang
Microcalorimetric measurements of the polymerization of actin in the presence of 100 mM KCl and 2 mM MgCl2were carried out with a Calvet MS-80 microcalorimeter at temperatures from 293.15 to 310.15 K. It was observed that the polymerization
of actin was endothermic and the enthalpy change for actin polymerization was temperature-dependent. The enthalpy change ΔHowas fitted to ΔHo(kJ mol-1)=434.0-1.16 (T/K) and the change in heat capacity ΔCpocalculated from ΔHowas -1.16 kJ (mol K)-1in the above range of temperatures. The direct calorimetry results showed that the enthalpy and entropy change for actin polymerization
could not be obtained from measurements of the critical concentration and the only way to assess the enthalpy change for the
polymerization of actin and similar reactions lies in the use of calorimetry.
Authors:J. Shao, Y. Yang, B. Li, L. Zhang, Y. Chen, and X. Liu
Two compounds of antimony trichloride and bismuth trichloride with valine are synthesized by solid phase synthesis at room
temperature. Their compositions, determined by element analysis, are Sb(C5H10O2N)3·2H2O and Bi(C5H10O2N)2Cl·0.5H2O. The crystal structure of antimony complex with valine belongs to triclinic system and its lattice parameters are: a=0.9599 nm, b=1.5068 nm, c=1.9851 nm, α=92.270, β=95.050, γ=104.270. The crystal structure of bismuth complex with valine belongs to monoclinic system
and its lattice parameters are: a=1.6012 nm, b=1.8941 nm, c=1.839 nm, β=99.73°. The far-infrared spectra and infrared spectra show that the amino group and carboxyl of valine may be
coordinated to antimony and bismuth, respectively, in two compounds. The TG-DSC results also reveal that the complexes were
Authors:C.L. Liu, X.Y. Wang, Z.M. Wang, S.S. Li, C.T. Xin, H.F. Wang, B. Li, and L. Jiang
The migration of 99Tc in a weak loess aquifer was investigated in-situ with undisturbed aquifer medium columns. The columns were obtained horizontally at a depth of 3236 m in an Underground Research Facility (URF). Quartz containing 3H (HTO) and 99Tc (in the form of 99TcO4-) was introduced into one end of the columns and the columns were covered tightly. Aquifer water was introduced into the columns directly from an experimental shaft in the UFR. Effluents from the columns were collected and the activity of 3H and 99Tc were determined with a liquid scintillation analyzer. The breakthrough curves of 3H and 99Tc indicate that 99Tc migrates a little faster than that 3H does in the aquifer.