The low-temperature heat capacity Cp,m of erythritol (C4H10O4, CAS 149-32-6) was precisely measured in the temperature range from 80 to 410 K by means of a small sample automated adiabatic
calorimeter. A solid-liquid phase transition was found at T=390.254 K from the experimental Cp-T curve. The molar enthalpy and entropy of this transition were determined to be 37.92±0.19 kJ mol−1 and 97.17±0.49 J K−1 mol−1, respectively. 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 standard
molar enthalpy of combustion and the standard molar enthalpy of formation of the compound have been determined: ΔcHm0(C4H10O4, cr)= −2102.90±1.56 kJ mol−1 and ΔfHm0(C4H10O4, cr)= − 900.29±0.84 kJ mol−1, by means of a precision oxygen-bomb combustion calorimeter at T=298.15 K. DSC and TG measurements were performed to study the thermostability of the compound. The results were in agreement
with those obtained from heat capacity measurements.
Molar heat capacities
of acetaminophen were precisely measured with a small sample precision automated
adiabatic calorimeter over the temperature range from 80 to 330 K. A solid-solid
transition at 149.96 K was found from the Cp,m-T curve. The polynomial functions of Cp,.m(J
K-1 mol-1) vs. T were established
on the heat capacity measurements by means of the least square fitting method.
processes of acetaminophen have been studied by thermogravimetry. And the
thermal decomposition kinetics parameters, such as activation energy E, pre-exponential factor A
and reaction order n, were calculated by
TG-DTG techniques with the Freeman-Carroll method, Kissinger method
and Ozawa method. Accordingly the thermal decomposition kinetics equation
of acetaminophen is expressed as: dα/dt=2.67107e-89630/RT(1-α)0.23.
The process of fusion has been investigated through
DSC. The melting point, molar enthalpy and entropy of fusion are to be (441.890.04)
K, 26.490.44 kJ mol-1 and 59.801.01
J K-1 mol-1,
A simple direct labeling method was used to synthesize the iodinated ultrafine polystyrene particles. The assay of X-ray photoelectron
spectroscopy (XPS) as well as Fourier-transform infrared (FT-IR) spectroscopy indicated the formation of stable covalent bond
to aryl group of the polymer particles. The purified radioiodinated product was incubated with serum of rat, and then evaluated
by in vitro stability test. The result showed that these synthesized ultrafine polystyrene particles were unmetabolized at
2 hours post-exposure, indicating the potential useful application of this labeled polymer particles as a promising probe
in biomedical sciences.
Authors:Guo Zhijun, Niu Yanning, Zhang Weiguang, and Tan Minyu
N,N,N',N',N'',N''-Hexaethyl-2,2′,2''-(nitrilotrisethyleneoxy-2-benzyloxy)tris(acetamide) (L3) has been prepared and characterized
by using IR, 1H NMR and positive-ion FAB mass spectra. The extraction of Th4+ and UO22+ with N,N,N',N',N'',N''-hexaethyl-2,2',2''- (nitrilo-trisethyleneoxy)tris(acetamide) (L1), N,N,N',N',N'',N''-hexaisopropyl-2,2',2''-(nitrilotrisethyleneoxy)tris(acetamide)
(L2), and L3 was studied at 20±1 °C as a function of diluent, concentration of free extractant in organic phase and concentration
of picrate in aqueous phase. It was found that the extracting powers of L1 and L2 for Th4+ are almost identical. The extracting power of L2 for UO22+ was slightly higher than that of L1. The difference in terminal
groups (ethyl or isopropyl) of the extractants (L1 and L2) with same backbone has a little effect on the extracting power
for both Th4+ and UO22+. The extracting powers of L3 for both Th4+ and UO22+ were larger than those of L1 and L2. The extractants
(L1 and L3) having the same terminal group (ethyl) with different backbones have obviously different extracting powers for
Th4+ or UO22+. The extracting powers of all three extractants L1, L2, and L3 for Th4+ were larger than those for UO22+. The
compositions of extracted species in organic phase were predominantly ThL(Pic)3NO3 and UO2L(Pic)NO3, respectively (L denotes
L1, L2 and L3).
A fully automated adiabatic calorimeter controlled on line by a computer used for heat capacity measurements in the temperature
range from 80 to 400 K was constructed. The hardware of the calorimetric system consisted of a Data Acquisition/Switch Unit,
34970A Agilent, a 7 1/2 Digit Nano Volt /Micro Ohm Meter, 34420A Agilent, and a P4 computer. The software was developed according
to modern controlling theory. The adiabatic calorimeter consisted mainly of a sample cell equipped with a miniature platinum
resistance thermometer and an electric heater, two (inner and outer) adiabatic shields, two sets of six junction differential
thermocouple piles and a high vacuum can. A Lake Shore 340 Temperature Controller and the two sets of differential thermocouples
were used to control the adiabatic conditions between the cell and its surroundings. The reliability of the calorimeter was
verified by measuring the heat capacities of synthetic sapphire (α-Al2O3), Standard Reference Material 720. The deviation of the data obtained by this calorimeter from those published by NIST was
within ±0.1% in the temperature range from 80 to 400 K.
Authors:X. Liu, H. Zhang, Z. Tan, K. Han, and L. Sun
The isoquinoline alkaloids were isolated from traditional Chinese drugs of Phellodendri Cortex, Radix Stephaniae Tetrandrae,
Corydalis Yanhusuo and Corydalis Bungeana. The power-time curves of growth of E. coli at different concentrations of isoquinoline alkaloid at 37�C were determined by a 2277 Thermal Activity Monitor. The rate
constant of bacteriostastic activity was calculated. The relationship between growth rate constant and concentration was established.
The optimum bacteriostastic concentration was determined. Experimental results have indicated that all the isoquinoline alkaloids
isolated from the four kinds of traditional Chinese drugs have bacteriostastic activity and the order is Phellodendri Cortex>Radix
Stephaniae Tetrandrae>Corydalis Yanhusuo>Corydalis Bungeana.
Authors:Ling Zhang, Huan Zhao, Qiushi Li, Juan Wang, and Xin Tan
An article assessment system based on both Tianjin University and nine key Chinese Universities’ academic disciplinary benchmarks
was established to evaluate researcher’s published papers. With this scientific benchmarking system, the quality of a researcher’s
papers could be easily located in a percentile scale in corresponding field within certain groups. Several factors, including
total number of papers, order of authors, impact of journals, citation count, h-index, e-index, a-index, m-quotient, etc.,
were also utilized for both quantity and quality analysis. Furthermore, the novel proposed weighted citation analysis was
introduced to judge a researcher’s contribution to his/her research outcomes. The convenient application and comprehensive
evaluation property of this assessment system was thoroughly discussed via a given example.
Authors:Zhi-Cheng Tan, Ji-Biao Zhang, and Meng Shang-He
A computerized adiabatic calorimeter for heat capacity measurements in the temperature range 80–400 K has been constructed.
The sample cell of the calorimeter, which is about 50 cm3 in internal volume, is equipped with a platinum resistance thermometer and surrounded by an adiabatic shield and a guard
shield. Two sets of 6-junction chromel-copel thermocouples are mounted between the cell and the shields to indicate the temperature
differences between them. The adiabatic conditions of the cell are automatically controlled by two sets of temperature controller.
The reliability of the calorimeter was verified through heat capacity measurements on the standard reference material α-Al2O3. The results agreed well with those of the National Bureau of Standards (NBS): within 0.2% throughout the whole temperature
region. The heat capacities of high-purity graphite and polystyrene were precisely measured in the interval 260–370 K by using
the above-mentioned calorimeter. The results were tabulated and plotted and the thermal behavior of the two materials was
discussed in detail. Polynomial expressions for calculation of the heat capacities of the two substances are presented.
Authors:Fu Shuren, Zhang Guanghua, Tan Qun, and Yang Yuqin
Thermal properties and morphology of crystal in NYLON 1010 formed isothermally at melting peak temperature were studied by
using DSC, TEM and ED. It turns out that the crystal on the time scale of the DSC experiment is stable, which is not transformed
from the crystal with low melting point. Its electron diffraction pattern shows symmetrical and clear electron diffraction
spots of single crystal and is proved to be the electron diffraction pattern of single crystal by means of index with parameters
of unit cell of Nylon 1010