Thermogravimetric Study of the M-Co-O System: I, M = Ta and Nb at 1200°C

Phase equilibria in the Ta-Co-O and Nb-Co-O systems have been studied at 1200°C at oxygen partial pressures from 10^−0.68 to 10^−13.50 atm for the former and from 10^−0.68 to 10^−13.30 atm for the latter. In both systems, M₂CoO₆ and M₂Co₄O₉ are stable ternary compounds under the experimental conditions, and a new phase, Nb₅Co₂O₁₄, has been identified. The Ta-Co-O system is simple, whereas the Nb-Co-O system is somewhat more complicated because of the extra phase. The lattice constants of the ternary compounds have been determined and compared with previous values. The standard Gibbs energies of reactions have been determined using oxygen partial pressures in equilibrium with three solid phases.     

Thermogravimetry and wide angle X-ray diffraction study on the structure of irradiated and thermally treated kodar film

The degradation behaviour of Kodar [poly(1,4-cyclohexylene dimethyl-eneterephthalate)] was investigated in air using thermogravimetry, differential thermal analysis and wide angle X-ray diffraction studies. The rates of crystallization and degradation were influenced by thermal exposure and polychromatic irradiation (Λ > 290 nm) for different time intervals. The crystallinity changes (X_c%) and activation energies (ΔE) for the systems have been determined.     

热分析在PVA纤维预处理中的应用

用差热、热重法对原丝的热性能及由不同预处理方法所引起的PVA纤维的热行为变化进行了研究;并通过模拟脱水条件,用不同升温速率,求出了经不同预处理纤维的脱水反应活化能。结果表明,PVA原丝在230℃有一软化点,三种预处理都不同程度地影响了原丝的热效应变化;纤维在180～340℃主要为脱水反应;原丝及经脱水剂、O_3和O_3综合脱水剂处理的纤维,其脱水反应的表观活化能分别为:164.3kJ/mol,92.9kJ/mol,130.5kJ/mol和117.6kJ/mol。     

EQUILIBRIA OF SYSTEM MoO_3-MoO_2-H_2O-H_2 AND PHASE DIAGRAM FOR SYSTEM Mo-O BETWEEN 400 AND 700℃

使用自行设计的受控气氛热重装置研究了MoO_3—MoO_2-H_2O—H_2系平衡.在P_(H_2O)/P_(H_2)从0.412至0.609,温度从400至534℃范围内直接测定了反应:MoO_3+H_2=MoO_2+H_2O(g)的平衡常数与温度间的关系为1gK_p=0.702-739.8/T获得298.15K下MoO_3标准生成焓及绝对熵分别为:-845.75kJmole~(-1)及78.1 J·K~(-1)mole~(-1) 实验表明,存在于MoO_2-MoO_3系中的一些Magneli相在本研究条件下不能作为热力学稳定相而存在.并绘制了400-700℃下Mo-O系相图.     

High-temperature oxidation of aluminum electroplated Fe-Mn alloys

Austenitic Mn-Al alloys (20–32 W/O Mn, 7–10 Al, 2–3 Si, 1C) were found to have satisfactory oxidation resistance up to 950°C under isothermal conditions in air. Surface enrichment of aluminum is a necessary condition for obtaining an almost pure alumina scale for uses at higher temperatures. Four different Mn-steels were Al-coated by the Capuano electroplating process. In all the steels there was an increase in the hot-oxidation resistance. The best results were obtained with steels containing both Al and Si, and this for temperatures up to 1100°C. No spalling was noticed during rapid cooling of the test pieces. Silicon was found to act as a diffusion barrier to outward iron diffusion. It appears that there is formation of a pure, thin film of alumina from the matrix which interacts with the aluminum diffusing from the superimposed, coating for the formation of good bonds.     

单组分阴离子水性聚氨酯胶膜的热质研究

应用热质分析（TG）研究了单组分阴离子水性聚氨酯胶膜的耐热性能，结果表明：n（--NCO）：n（--OH）增大，胶膜的耐热性能增强；聚酯相对分子质量增加，耐高温性能降低；用DEG扩链时的耐高温性能比用DEG／TMP时的好；TDI型水性聚氨酯成膜物的耐高温性能优于IPDI型水性聚氨酯。     

SIS-g-AN热降解性能的研究

采用热重分析法和差示热重分析法研究丙烯腈(AN)接枝热塑性弹性体SIS(SIS g AN)的热降解性能。结果得出,SIS g AN的平衡起始降解温度、平衡最大降解速率温度和平衡终止降解温度分别为659. 17, 713. 94 和740.05 K;热降解反应活化能为195.2 kJ·mol-1;热降解机理是Deceleration中的D3 降解机理;不同质量损失率下的热寿命与温度呈线性关系。     

超支化聚苯硫醚/聚苯硫醚共混纤维非等温结晶动力学及热性能研究

使用DSC方法研究了聚苯硫醚(PPS)以及超支化聚苯硫醚/聚苯硫醚共混纤维的非等温结晶动力学,分析了结晶峰值温度等参数,并用Ozawa方程和莫志深方程描述了非等温动力学。结果表明:超支化聚苯硫醚/聚苯硫醚共混纤维的非等温结晶动力学过程能够使用莫志深方程来描述。在共混过程中,少量的超支化聚苯硫醚在线型聚苯硫醚基体材料中能够起到成核剂的作用,提高结晶速率和结晶温度,减少结晶诱导期和半结晶时间。因此,超支化聚苯硫醚/聚苯硫醚共混纤维的结晶速率要快于纯聚苯硫醚纤维的结晶速率。热失重分析表明:超支化聚苯硫醚/聚苯硫醚共混纤维具有与纯聚苯硫醚纤维相同或更优良的热稳定性,添加超支化聚苯硫醚不会降低成品纤维的热稳定性。     

Volatility of Simulated High-Level Nuclear Waste Glass by Thermogravimetric Analysis

The volatilities of simulated, high-level nuclear waste glasses have been measured using thermogravimetric analysis (TGA). These volatilities were measured in the region of the glass transition temperature ( T _g) of the waste glasses, which is between 450° and 500°C. These data were obtained because the Waste Acceptance Preliminary Specifications require that no foreign materials be released into the canistered waste form upon heating of the canister to this glass transition temperature. In fact, all of the waste glass samples studied actually exhibited a net weight gain upon heating. This weight gain was shown to be due to oxygen uptake through oxidation of FeO. Powdered glass samples did show a small weight loss which was smaller in magnitude than the weight gain and was associated with water desorption. No true volatility was detected to the level of sensitivity (0.01 wt%) of the TGA instrument. This converts to a sensitivity of 330 μ g/m² of glass surface and a corresponding minimum value of 41 mg of volatiles for each Defense Waste Processing Facility conistered waste form. TGA experiments carried out at higher temperatures (800°C) revealed that organic concentrations in the waste glasses are less than 0.01 wt%. Thus, these results demonstrate that the Defense Waste Processing Facility will be able to comply with the Waste Acceptance Preliminary Specifications on the exclusion of foreign materials from the canistered waste forms, after exposure to T _g.     

Cinétique de dégagement des matières volatiles lors de la pyrolyse d'électrodes de carbone industrielles

In aluminium plants, the anode baking process is associated with an important release of volatile combustible matter. It is the purpose of this study to investigate the kinetics of the evolution of these volatiles. A large thermogravimetry set-up has been designed in such a way that it could simulate real plant conditions. Samples of two distinct masses have been subjected to pyrolysis at different heating regimes. The loss of weight together with the concentrations of the released gases were recorded on a continuous basis during the temperature rise. Kinetic results were found for methane, hydrogen and tar. No variation of the order of reaction with the heating rate was observed, whereas the activation energy and the pre-exponential factor increased. Furthermore, for the range of sample dimensions studied, it was found that the mass of the solid had no significant influence on the kinetic parameters.