The decomposition kinetics of reference calcite and three ultra-fine samples with different morphologies are investigated.
The kinetic parameters and rate equation are obtained according to the methods reported in our previous studies. Compared
with the reference calcite, a considerable diminution of the activation energy Ea up to 70–80 kJ mol−1 is observed in the case of three ultra-fine samples. There are also some distinct differences concerning the activation energy
of each of the ultra-fine sample. This may have something to do with the particle morphology revealed by TEM and SEM measurements.
XRD measurements of four calcite samples show that large strain exists in the crystal lattice in the case of ultra-fine calcite
samples. This may give a reason to their abnormal decomposition behavior.
A novel complex, [Pr(5-nip)(phen)(NO3)(DMF)]
(5-nip: 5-nitroisophthalic acid; phen: 1,10-phenanthroline, DMF: N,N-dimethylformamide),
was prepared and characterized by single crystal X-ray diffraction, elemental
analysis, IR spectrum and DTG-DSC techniques. The results show that the crystal
is monoclinic, space group P2(1)/n with a=11.0876(6) Å, b=12.8739(7)
Å, c=16.9994(8) Å; β=91.193(4)°, Z=4, Dc=1.822
Mg m–3, F(000)=1320.
Each Pr(III) ion is nine-coordinated by one chelating bidentate and two monodentate
bridging carboxylate groups, one chelating bidentate nitryl group, one DMF
molecule and one 1,10-phenanthroline molecule. The complex is constructed
with one-dimensional ribbons featuring dinuclear units and the one-dimensional
ribbons are further assembled into two-dimensional networks by strong π–π
stacking interactions. The complex has high stability up to 500°C. The
enthalpy change of formation of the compound in DMF was measured using an
RD496-III type microcalorimeter with the value of –9.214±0.173
Authors:X. Han, Y. Hu, Z. Lin, S. Li, F. Zhao, Z. Liu, J. Yi, L. Zhang, and X. Ren
Effects of fullerenes including FS, EFS and pure C60 on thermal behaviors of polyethylene glycol (PEG) have been studied by employing thermogravimetry-differential thermogravimetry
(TG-DTG), differential scanning calorimeter (DSC) and off-line furnace-type pyrolysis-gas chromatography/mass spectrometry
(Py-GC/MS). The products were collected by Cambridge filter pad which was widely used in analyzing the combustion products
of cigarette. The results showed that the addition of fullerenes obviously restrained the thermal decomposition of PEG. The
initial decomposition temperatures (IDT) and maximum decomposition peak temperatures (MDT) were evidently postponed by the
addition of fullerenes. Pyrolysis products with one or two hydroxyl end groups obviously increased with the addition of 10%
C60. The reasons of the changes were discussed from the aspects of reaction mechanisms.
Authors:X. Han, Y. Sun, T. Wang, Zh. Lin, Sh. Li, F. Zhao, Z. Liu, J. Yi, and X. Ren
The effects of fullerenes, including fellerene soot (FS), extracted fullerene soot (EFS) and pure C60 on the thermal decomposition of ammonium perchlorate (AP) compared with traditional carbon black (CB) catalyst has been studied
by employing thermogravimetry (TG), differential thermal analysis (DTA), infrared spectroscopy (IR) and ignition temperature
experiments. The results showed that the addition of CB and FS to AP reduced the activation energy as well as the temperature
at maximum decomposition rate, but that of EFS and pure C60 had little effect on the thermal decomposition of AP, and among all catalysts, FS was the best one.
Authors:H. L. Huo, S. H. Yu, X. Z. Liu, Y. Meng, Y. P. Ren, and L. T. Zhang
A selective and sensitive liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS) method was developed and validated for analysis of xanthotoxol (1), xanthotoxin (2), isoimpinellin (3), bergapten (4), oxypeucedanin (5), imperatorin (6), cnidilin (7), and isoimperatorin (8) in rat bile and urine using pimpinellin as an internal standard (IS). An Agilent 1200 liquid chromatography system (Agilent Technologies, USA) equipped with a quaternary pump, an autosampler, and a column compartment was used for all analyses. Chromatographic separations were performed on a Sapphire C18 column (150 mm × 4.6 mm, 5 μm), and the column temperature was maintained at 30°C; the sample injection volume was 10 μL. The specificity, linearity, accuracy, precision, recovery, matrix effect, and several stabilities were validated for all analytes in the rat bile and urine samples. The method was successfully applied in monitoring the concentrations of eight coumarins in rat bile and urine after a single oral administration of Radix Angelicae Dahuricae extract with a dosage of 8.0 mL/kg. In the bile samples, the eight coumarins excreted completely in twenty-four hours. The average percentages of coumarins (1–8) excreted were 0.045%, 0.019%, 0.177%, 0.105%, 0.337%, 0.023%, 0.024%, 0.021%. In the urine samples, the eight coumarins excreted completely in seventy-two hours. The average percentages of coumarins (1–8) excreted were 1.78%, 0.095%, 0.130%, 0.292%, 0.082%, 0.008%, 0.005%, 0.004%. The method is robust and specific and it can successfully complete the requirements of the excretion study of the eight coumarins in Radix Angelicae Dahuricae.
Authors:H. X. Ma, B. Yan, Y. H. Ren, Y. Hu, Y. L. Guan, F. Q. Zhao, J. R. Song, and R. Z. Hu
3,3-Dinitroazetidinium (DNAZ) salt of perchloric acid (DNAZ·HClO4) was prepared, it was characterized by the elemental analysis, IR, NMR, and a X-ray diffractometer. The thermal behavior and decomposition reaction kinetics of DNAZ·HClO4 were investigated under a non-isothermal condition by DSC and TG/DTG techniques. The results show that the thermal decomposition process of DNAZ·HClO4 has two mass loss stages. The kinetic model function in differential form, the value of apparent activation energy (Ea) and pre-exponential factor (A) of the exothermic decomposition reaction of DNAZ·HClO4 are f(α) = (1 − α)−1/2, 156.47 kJ mol−1, and 1015.12 s−1, respectively. The critical temperature of thermal explosion is 188.5 °C. The values of ΔS≠, ΔH≠, and ΔG≠of this reaction are 42.26 J mol−1 K−1, 154.44 kJ mol−1, and 135.42 kJ mol−1, respectively. The specific heat capacity of DNAZ·HClO4 was determined with a continuous Cp mode of microcalorimeter. Using the relationship between Cp and T and the thermal decomposition parameters, the time of the thermal decomposition from initiation to thermal explosion (adiabatic time-to-explosion) was evaluated as 14.2 s.
Two lines, L-19-613 and L-19-626, were produced from the common wheat cultivar Longmai 19 (L-19) by six consecutive backcrosses using biochemical marker-assisted selection. L-19 (Glu-D1a, Glu-A3c/Gli-A1?; Gli-A1? is a gene coding for unnamed gliadin) and L-19-613 (Glu-D1d, Glu-A3c/Gli-A1?) formed a set of near-isogenic lines (NILs) for HMW-GS, while L-19-613 and L-19-626 (Glu-D1d, Glu-A3e/Gli-A1m) constituted another set of NILs for the LMW-GS/gliadins. The three L-19 NILs were grown in the wheat breeding nursery in 2007 and 2008. The field experiments were designed using the three-column contrast arrangement method with four replicates. The three lines were ranked as follows for measurements of gluten strength, which was determined by the gluten index, Zeleny sedimentation, the stability and breakdown time of the farinogram, the maximum resistance and area of the extensogram, and the P andWvalues of the alveogram: L-19-613 > L-19-626 > L-19. The parameters listed above were significantly different between lines at the 0.05 or 0.01 level. The Glu-D1 and Glu-A3/Gli-A1 loci had additive effects on the gluten index, Zeleny sedimentation, stability, breakdown time, maximum resistance, area, P and W values. Although genetic variation at the Glu-A3/Gli-A1 locus had a great influence on wheat quality, the genetic difference between Glu-D1d and Glu-D1a at the Glu-D1 locus was much larger than that of Glu-A3c/Gli-A1? and Glu-A3e/Gli-A1m at the Glu-A3/Gli-A1 locus. Glu-D1d had negative effects on the extensibility and the L value compared with Glu-D1a. In contrast, Glu-A3c/Gli-A1? had a positive effect on these traits compared with Glu-A3e/Gli-A1m.