Lanzhou Alkaline Stretched Noodles (LASN) has introduced by Meng et al. in previous research paper (2007). In order to discover the LASN specialty wheat quality requirement for allelic variations at
of northwest China spring wheats, 2 northwest China spring wheat cultivars and 39 elite F6 breeding lines were adopted to determine the high-molecular-weight glutenin subunits (HMW-GS) composition by one step one-dimensional sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) based on the protocol of Singh et al. (1991). The results showed that the wheat quality and LASN quality were characterised by
/1 correlated to high protein content and better extensibility (L) than other allelic variations.
/5+10 were beneficial to dough strength (W), meanwhile
/5+10 were good to dough tenacity (P).
/5+10 strongly correlated to high volume of SDS-sediment significantly. Allelic variations at
/ (1, 2*),
/5+10 were beneficial alleles for wheat quality as well as LASN quality. However,
/2+12 were inferior alleles for wheat quality and LASN quality.
Authors:G. Xie, S. Chen, S. Gao, X. Meng, and Q. Shi
A novel solid complex, formulated as Ho(PDC)3
(o-phen), has been obtained from the reaction
of hydrate holmium chloride, ammonium pyrrolidinedithiocarbamate (APDC) and
in absolute ethanol, which was characterized by elemental analysis, TG-DTG
and IR spectrum. The enthalpy change of the reaction of complex formation
from a solution of the reagents, ΔrHmθ (sol), and the molar heat capacity of the complex, cm,
were determined as being –19.1610.051 kJ mol–1
and 79.2641.218 J mol–1 K–1
at 298.15 K by using an RD-496 III heat conduction microcalorimeter. The enthalpy
change of complex formation from the reaction of the reagents in the solid
phase, ΔrHmθ(s), was calculated as
being (23.9810.339) kJ mol–1 on the
basis of an appropriate thermochemical cycle and other auxiliary thermodynamic
data. The thermodynamics of reaction of formation of the complex was investigated
by the reaction in solution at the temperature range of 292.15–301.15
K. The constant-volume combustion energy of the complex, ΔcU, was determined as being –16788.467.74
kJ mol–1 by an RBC-II type rotating-bomb
calorimeter at 298.15 K. Its standard enthalpy of combustion, ΔcHmθ, and standard enthalpy of formation,
ΔfHmθ, were calculated to be –16803.957.74 and –1115.428.94
kJ mol–1, respectively.
Authors:X. Zeng, Y. Chen, S. Cheng, X. Meng, and Q. Wang
A novel method for the determination of rate constants of reactions, the time-variable method, is proposed in this paper. The method needs only three time points (t), peak heights () and pre-peak areas (), obtained from the measured thermoanalytical curve. It does not require the thermokinetic reaction to be completed. It utilizes data-processing on a computer to give the rate constants. Four reaction systems, including a first-order reaction, second-order reactions (with equal concentrations and with unequal concentrations) and a third-order reaction, were studied with this method. The method was validated and its theoretical basis was verified by the experimental results.
The heat capacities of chrysanthemic acid in the temperature range from 80 to 400 K were measured with a precise automatic
adiabatic calorimeter. The chrysanthemic acid sample was prepared with the purity of 0.9855 mole fraction. A solid-liquid
fusion phase transition was observed in the experimental temperature range. The melting point, Tm, enthalpy and entropy of fusion, ΔfusHm, ΔfusSm, were determined to be 390.7410.002 K, 14.510.13 kJ mol-1, 37.130.34 J mol-1 K-1, respectively. The thermodynamic functions of chrysanthemic acid, H(T)-H(298.15), S(T)-S(298.15) and G(T)-G(298.15) were reported with a temperature interval of 5 K. The TG analysis under the heating rate of 10 K min-1 confirmed that the thermal decomposition of the sample starts at ca. 410 K and terminates at ca. 471 K. The maximum decomposition
rate was obtained at 466 K. The purity of the sample was determined by a fractional melting method.
The catalytic and accelerating effects of three coal-burning additives (CBA) on the burning of graphite were studied with
the help of thermogravimetric (TG) analysis. The kinetic study on the catalytic oxidation of the graphite doped with CBA was
carried out and the results were presented. The results show that the CBA can change the carbon oxidation/combustion course
by catalytic action and change the activation energy, thus improving the combustion efficiency.
Authors:L. Wang, Z. Tan, S. Meng, D. Liang, S. Ji, and Z. Hei
Fe–B ultrafine amorphous alloy particles (UFAAP) were prepared by chemical reduction of Fe3+ with NaBHO4 and confirmed to be ultrafine amorphous particles by transmission electron microscopy and X-ray diffraction. The specific
heat of the sample was measured by a high precision adiabatic calorimeter, and a differential scanning calorimeter was used
for thermal stability analysis. A topological structure of Fe-B atoms is proposed to explain two crystallization peaks and
a melting peak observed at T=600, 868 and 1645 K, respectively.
Authors:S. Chen, X. Meng, Q. Shuai, B. Jiao, S. Gao, and Q. Shi
solid complex Eu(C5H8NS2)3(C12H8N2) has been obtained from reaction of
hydrous europium chloride with ammonium pyrrolidinedithiocarbamate (APDC)
and 1,10-phenanthroline (o-phen⋅H2O)
in absolute ethanol. IR spectrum of the complex indicated that Eu3+
in the complex coordinated with sulfur atoms from the APDC and nitrogen atoms
from the o-phen. TG-DTG investigation provided
the evidence that the title complex was decomposed into EuS.
enthalpy change of the reaction of formation of the complex in ethanol, ΔrHmθ(l), as –22.2140.081 kJ mol–1,
and the molar heat capacity of the complex, cm,
as 61.6760.651 J mol–1 K–1,
at 298.15 K were determined by an RD-496 III type microcalorimeter. The enthalpy
change of the reaction of formation of the complex in solid, ΔrHmθ(s), was calculated as 54.5270.314 kJ mol–1
through a thermochemistry cycle. Based on the thermodynamics and kinetics
on the reaction of formation of the complex in ethanol at different temperatures,
fundamental parameters, including the activation enthalpy (ΔH≠θ),
the activation entropy (ΔS≠θ),
the activation free energy (ΔG≠θ),
the apparent reaction rate constant (k),
the apparent activation energy (E), the
pre-exponential constant (A) and the reaction
order (n), were obtained. The constant-volume
combustion energy of the complex, ΔcU,
was determined as –16937.889.79 kJ mol–1
by an RBC-II type rotating-bomb calorimeter at 298.15 K. Its standard enthalpy
of combustion, ΔcHmθ,
and standard enthalpy of formation, ΔfHmθ,
were calculated to be –16953.379.79 and –1708.2310.69
kJ mol–1, respectively.
Authors:P. Yu, Z. Tan, S. Meng, S. Lu, X. Lan, L. Sun, F. Xu, T. Zhang, and S. Hu
Isoproturon [N'-(p-cumenyl)-N,N-dimethylurea] was synthesized, and the low-temperature heat capacities were measured with a small sample precise
automatic adiabatic calorimeter over the temperature range from 78 to 342 K. No thermal anomaly or phase transition was observed
in this temperature range. The melting and thermal decomposition behavior of isoproturon was investigated by thermogravimetric
analysis (TG) and differential scanning calorimetry (DSC). The melting point and decomposition temperature of isoproturon
were determined to be 152.4 and 239.0C. The molar melting enthalpy, and entropy of isoproturon, ΔHm and ΔSm, were determined to be 21.33 and 50.13 J K-1 mol-1, respectively. The fundamental thermodynamic functions of isoproturon relative to standard reference temperature, 298.15
K, were derived from the heat capacity data.
Authors:J. Zhang, Z. Tan, Q. Meng, Q. Shi, B. Tong, and S. Wang
The heat capacities (Cp,m) of 2-amino-5-methylpyridine (AMP) were measured by a precision automated adiabatic calorimeter over the temperature range
from 80 to 398 K. A solid-liquid phase transition was found in the range from 336 to 351 K with the peak heat capacity at
350.426 K. The melting temperature (Tm), the molar enthalpy (ΔfusHm0), and the molar entropy (ΔfusSm0) of fusion were determined to be 350.431±0.018 K, 18.108 kJ mol−1 and 51.676 J K−1 mol−1, respectively. The mole fraction purity of the sample used was determined to be 0.99734 through the Van’t Hoff equation.
The thermodynamic functions (HT-H298.15 and ST-S298.15) were calculated. The molar energy of combustion and the standard molar enthalpy of combustion were determined, ΔUc(C6H8N2,cr)= −3500.15±1.51 kJ mol−1 and ΔcHm0 (C6H8N2,cr)= −3502.64±1.51 kJ mol−1, by means of a precision oxygen-bomb combustion calorimeter at T=298.15 K. The standard molar enthalpy of formation of the crystalline compound was derived, ΔrHm0 (C6H8N2,cr)= −1.74±0.57 kJ mol−1.
Authors:Y.-J. Song, S.-H. Meng, F.-D. Wang, C.-X. Sun, and Z.-C. Tan
Polyimide BTDA-ODA sample was prepared by polycondensation or step-growth polymerization method. Its low temperature heat capacities were measured by an adiabatic calorimeter in the temperature range between 80 and 400 K. No thermal anomaly was found in this temperature range. A DSC experiment was conducted in the temperature region from 373 to 673 K. There was not phase change or decomposition phenomena in this temperature range. However two glass transitions were found at 420.16 and 564.38 K. Corresponding heat capacity increments were 0.068 and 0.824 J g–1 K–1, respectively. To study the decomposition characteristics of BTDA-ODA, a TG experiment was carried out and it was found that this polyimide started to decompose at ca 673 K.