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1.
Poly(ethylene aspartate) [PEA] was synthesized by the melt condensation of D,L-aspartic acid and ethylene glycol. PEA containing pendent amino and carbonyl groups in its repeating chain was used as the polymeric ligand for complexation with transition metal ions, viz. Co(II), Ni(II), Cu(II), Mn(II), Zn(II), Cd(II), Ca(II), Mg(II), Pb(II) and Hg(II). Complexation was found to be most effective in DMSO. The resulting polyester-metal complexes were solid coloured materials which have been characterized by IR spectroscopy, elemental analysis and magnetic susceptibility measurements. The thermal stability of the polyester-metal complexes was investigated by thermogravimetric analysis (TGA). On the basis of the physico-chemical studies, an oxygen and nitrogen coordinated structure for the polyester-metal complexes is proposed. 相似文献
2.
The interaction of different metal oxides such as Co3O4, NiO, Al2O3, Cr2O3, Fe2O3 and SiO2 with Na2SO4 at a temperature of 1100 and 1200 K in flowing oxygen has been studied. The thermogravimetric studies for each system were
carried out as a function of Na2SO4 in the mixture. The presence of different constituents in the reaction products were identified by X-ray diffraction analysis
and the morphologies of the reaction products were characterized using metallography and scanning electron microscopy (SEM).
The formation of products was also investigated by thermodynamic computation of free energies of the reactions and the study
of relevant equilibrium phase diagrams. The soluble species in the aqueous solutions of the reaction products were determined
quantitatively using atomic absorption spectrophotometry.
The high temperature interaction products usually contain a 3-phase structure namely, Na2O·M2O
x
, M2O
x
and metal sulphide and/or metal sulphate. The formation of Na2O·M2O
x
depends upon the solid state solubility of metal oxide in the molten salt at high temperatures. Under limited solubility
conditions Na2O·M2O
x
is invariably formed, but as soon as this condition is relaxed the oxide. M2O
x
, precipitates and forms a separate phase. 相似文献
3.
采用示差扫描量热和热重分析的方法对合成的不同4,4'-二苯醚二甲酸(OBBA)含量的共聚酯的热性能进行了研究。结果发现共聚酯的熔点和热结晶温度与PET相比有所降低;而冷结晶温度则升高。随着OBBA添加量的增加,在恒温热重分析中热失重速率常数减小;在升温热重分析中,热失重活化能则增加。所有的实验结果皆表明,芳族醚键的引入对提高共聚酯的热性能有重要作用。 相似文献
4.
T. S. Radhakrishnan 《应用聚合物科学杂志》2006,99(5):2679-2686
Thermal degradation of poly(dimethylsilylene) homopolymer (PDMS) and poly(tetramethyldisilylene‐co‐styrene) copolymer (PTMDSS) was investigated by pyrolysis‐gas chromatography and thermogravimetry (TG). PDMS decomposes by depolymerization, producing linear and cyclic oligomeric products, whereas PTMDSS decomposes by random degradation along the chain resulting in each monomeric product and various other combination products. The homopolymer was found to be much less stable than the copolymer. The decomposition mechanisms leading to the formation of various products are shown. The kinetic parameters of thermal degradation were evaluated by different integral methods using TG data. The activation energies of decomposition (E) for the homopolymer and the copolymer are found to be 122 and 181 kJ/mol, respectively, and the corresponding values of order of reaction are 1 and 1.5. The observed difference in the thermal stability and the values of the kinetic parameters for decomposition of these polymers are explained in relation with the mechanism of decomposition. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006 相似文献
5.
热重分析对高分子材料中碳酸钙的定量研究 总被引:1,自引:0,他引:1
碳酸钙是高分子材料中常用的无机填料,在高温时会同二氧化碳而失重。利用热重分析可准确定出高分子材料中碳酸钙的含量,同时还可测出聚合物,挥发物的含量,热重分析法样品用量小,灵敏度高,所需时间短。 相似文献
6.
Ti-45Al-10Nb合金的高温氧化行为 总被引:4,自引:0,他引:4
研究了Ti—45A1—10Nb(原子分数,%)合金在800-960℃在氧气和空气中的氧化行为.结果表明,该合金具有较好的高温抗氧化性能,其氧化增重速率与铁基耐热不锈钢相似或略优.与Ti—50A1合金相反,Ti-45A1-10Nb合金在空气中的氧化增重速率明显低于在纯氧中的氧化增重速率.X射线衍射与能谱分析表明,Ti-45Al一10Nb合金在氧气中的氧化产物主要有TiO2和Al2O3,但在空气中的氧化产物中有TiN相.这是降低氧化速率的主要原因,同时,合金元素Nb稳定了氧化层中的TiN相,因而提高了合金在空气中的抗氧化性能. 相似文献
7.
8.
石灰石分解反应的热重动力学研究 总被引:3,自引:0,他引:3
用热重分析等研究方法,对我国9个主要产地的石灰石矿样品进行了大量的实验和分析工作,并分别计算出不同产地石灰石的动力学数据。 相似文献
9.
The N‐[3‐(dimethoxy‐methyl‐silanyl)‐propyl]‐N′‐ (9‐methyl‐3,9‐dioxo‐2,4,8,10‐tetraoxa‐3,9‐diphospha‐spiro[5.5]undec‐3‐yl)‐ethane‐1,2‐diamine/dimethoxy dimethyl silane copolymer (PSiN II), which simultaneously contains silicon, phosphorus, and nitrogen, is synthesized and incorporated into polypropylene (PP). The flame retardancy is evaluated by the limiting oxygen index value, which is enhanced to 29.5 from 17.4 with 20% total loading of PSiN II. The thermal degradation behavior of PP/PSiN II is investigated by thermogravimetric analysis under N2 and air. The PP/PSiN II sample degrades at 400°C for different amounts of time, and the process of degradation is studied by Fourier transform IR. The morphology of the char formed at 400°C for 10 min is investigated by scanning electron microscopy. The swollen inner structure, close, and smooth outer surface provide a much better barrier for the transfer of heat and mass during fire and good flame retardancy. The thermal stability of PP is improved by incorporation of PSiN II. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2487–2492, 2005 相似文献
10.
The thermal degradation of poly(vinyl butyral) (PVB)/glass ceramic, PVB/Ag, and PVB/glass ceramic/Ag composites was investigated with thermogravimetric analysis in nitrogen and air. Thermogravimetric data revealed that the compositions of both inorganic materials in air could greatly influence the thermal degradation of PVB. The degradation reactions of PVB/ceramic and PVB/Ag composites began earlier and accelerated rapidly at lower temperatures. The overall degradation period was obviously shortened for the thermal degradation of PVB/Ag in air, whereas a longer time was required for the PVB/ceramic composite than for PVB. Moreover, dual effects of ceramic and Ag on the thermal degradation of PVB were observed for PVB/ceramic/Ag composites. In addition, the catalytic effects of ceramic and Ag on the degradation reaction of PVB in air were verified with a kinetic analysis. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2142–2149, 2004 相似文献