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131.
水溶性聚酯的结构和性能 总被引:2,自引:0,他引:2
由对苯二甲酸二甲酯、间苯二甲酸、间苯二甲酸二甲酯5-磺酸钠与乙二醇等共缩聚合成的PET型水溶性聚酯(WSP)是一种新型的水溶性聚合物,在化纤、纺织、涂料、粘合剂、电子、油墨等领域有着广泛的应用前景.化纤领域超细纤维新材料的研究、开发和生产,迫切需要一... 相似文献
132.
The investigated materials have similar routes of thermal decomposition; i.e. they lose their crystal water first, then at
a higher temperature their structural one. At least the result TiP2O7 goes through a phase change at about 1000 K. The amorphous titanium phosphate lost its crystal and structural water at higher
temperature than those of crystalline forms. Both α- and γ-titanium phosphates and also their transition metal containing
forms have layered structure. In case of α- and γ-forms after the loss of crystal water a phase change occurs which is followed
by the decomposition of the molecule. Various transition metals containing γ-titanium phosphates lose their crystal water
at the same temperature, with the exception of Ni containing ones. The process is finished in this case at temperature 90
K higher than that of the others.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
133.
建立了散射背景下测定人体血清中Zn^2+含量的激光热透镜光谱分析方法。比较了蛋白质微粒散射对于分光光度法和激光热透镜光谱分析法测定的影响。结果表明,激光热透镜光谱分析方法能够避免溶液中存留蛋白质微粒散射的影响。Zn^2+量在0~1.6μg/mL范围内呈线性关系(r=0.9986),检出限为1ng/mL。应用于人体血清中Zn^2+含量的测定,与原子吸收法测定结果基本一致。 相似文献
134.
纳米PbSnO3的制备及其燃烧催化性能的研究 总被引:1,自引:0,他引:1
Nanocomposite PbSnO3was synthesized by coprecipitation method , and its phase evolution process was investigated. The particle size, crystal form, and phase of samples were determined with XRD, TEM and EDS. The catalytic actiyity of sample on the thermal decomposition of RDX was investigated by DSC. The results show that nanocomposite PbSnO3with the diameter of 9 nm can be obtained by calcining at 600 ℃ for 2 h, which crystal is cubic (pyrochlore type). The catalytic actiyity of nanocomposite PbSnO3on the thermal decomposition of RDX is much higher than that of normal PbSnO3. The nanocomposite PbSnO3can decrease the peak temperature of thermal decomposition of RDX from 240.1 ℃ to 236.5 ℃, and the decomposition enthalpy ΔH of RDX increases 722 J·g-1 (about 70%). 相似文献
135.
Chemometric techniques have been applied to FTIR and DSC data to correlate polymer composition. Since structural differences
in the polymers with only hydrocarbon structure, often cause subtle changes in spectra, the ability of chemometric techniques
is required to discern these differences. FTIR spectra and thermal fractionation using DSC were measured for 28 types of polyethylenes
(PE) varying in chain branching type, content and distribution. Unsupervised clustering methods such as principal component
analysis (PCA) and supervised discriminant analysis were used to classify the PEs according to their structural class. The
DSC data was the more successful in both classifying PEs according to their class.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
136.
Vora A. Riga A. Dollimore D Alexander K. 《Journal of Thermal Analysis and Calorimetry》2004,75(3):709-717
This study attempts to identify the degradative process which folic acid undergoes in the solid-state under thermal stress.
In order to facilitate the process, the various pieces of the chemical structure, namely, p-amino benzoic acid, pterin and glutamic acid as both its d- and l-isomers were investigated as separate entities. These structured solid-state pieces were then compared to the composite solid
state folic acid degradative curves in order to identify the peaks seen and provide direction for the interpolation of the
degradative mechanism. It was observed that none of the structural pieces could be superimposed as assumed earlier and hence
an attempt was made to identify the decomposition products using various analytical techniques such as infrared spectroscopy,
mass spectroscopy and X-ray diffraction which suggested that the glutamic acid fragment is lost first as evidenced by acid
loss and amide enhancement in the IR spectra. The vitamin was ultimately degrading to carbon fragments and that further identification
was not necessary.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
137.
H. M. Parekh P. K. Panchal M. N. Patel 《Journal of Thermal Analysis and Calorimetry》2006,86(3):803-807
Some new coordination polymers of Mn(II),
Co(II), Ni(II), Cu(II), Zn(II) and Cd(II), obtained from the interaction of
metal acetate with dipotassium salt of N,N’-di(carboxyethylidene)terephthalaldehydediimine
(K2SB) are described. The products, which have been
characterized by elemental analyses, magnetic measurements, thermogravimetric
analyses, electronic and infrared spectral studies, have composition, [M(SB)(H2O)2]n. These colored coordination polymers are non-hygroscopic and quite stable
at room temperature. On the basis of analytical data and IR studies, a 1:1
metal to ligand stoichiometry has been suggested to these coordination polymers.
The IR studies have also revealed that ligands are coordinated to metal ion
through carboxy oxygen and azomethine nitrogen. All the studies suggested
tetradentate nature of the ligand with octahedral symmetry of the coordination
polymers. All the coordination polymers are insoluble in acetone, ethanol,
chloroform, methanol, benzene, DMF and DMSO. The thermal decomposition of
the coordination polymers is studied and indicates that not only the coordinated
water is lost but also that the decomposition of the ligand from the coordination
polymers is necessary to interpret the successive mass loss. 相似文献
138.
The effects of temperature and duration of melting on the rate of isothermal crystallization of isotactic polypropylene were investigated by differential scanning calorimetry (DSC). Crystallization rates were found to decrease with increasing melt temperature and melting time. The results were discussed in the framework of the theoretical model of transient isothermal crystallization developed by the present authors [1]. The results suggest gradual destruction of predetermined nuclei with activation energyE
a=89±7 kJ/mole as a main mechanism of the observed effects.This work and Part I of this research [1] have been supported in part by Research Grant Number PB 1291/52/93/04 from State Committee for Scientific Research (KBN), Poland, and by 40% MURST founds, Italy. 相似文献
139.
《Surface and interface analysis : SIA》2005,37(8):683-688
Heating (100) silicon at high temperature (say, higher than 850 °C) in H2, cooling to 670–700 °C in the same ambient, and quenching to room temperature in N2 results in environmentally robust, terraced 1 × 1 (100) SiH2. Evidence for this conclusion is based on angle‐resolved x‐ray photoelectron spectroscopy, atomic force microscopy, infrared absorption spectroscopy in the attenuated total reflection mode, thermal programmed desorption, and reflection high‐energy electron diffraction. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
140.
Synthesis, Characterization and Thermal Decomposition Mechanism of Cetyltrimethyl Ammonium Tetrathiotungstate 总被引:2,自引:0,他引:2
Gaojun An Yunqi Liu Yongming Chai Hongyan Shang Chenguang Liu 《天然气化学杂志》2006,15(2):127-133
The synthesis, characterization and thermal decomposition mechanism of cetyltrimethyl ammonium tetrathiotungstate (CTriMATT) were studied herein. The as-synthesized CTriMATT was characterized by Elemental analysis, X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Ultraviolet visible (UV-Vis) spectra. The results showed that the as-synthesized CTriMATT had high purity and good crystallinity. The introduction of alkyl groups induced a shift of the stretching vibration band of W-S bond to lower wavenumber, while it had no influence on the position of WS4^2-. Thermogravimetric analysis (TG), differential thermal analysis (DTA) and in situ XRD characterizations revealed that CTriMATT began to decompose at 423 K in nitrogen and was converted to WS2 eventually. In addition, the decomposition product of CTriMATT at 673 K in nitrogen was characterized by N2 adsorption (BET) and scanning electron microscopy (SEM). The results demonstrated that WS2 with higher specific surface area, and pore volume could be obtained from the thermal decomposition of CTriMATT in nitrogen. 相似文献