利用TG-FTIR联用技术对Kevlar纤维的热解过程的分析

现代工业应用与技术领域要求材料具有良好的机械性质与热学性质,Kevlar纤维做为近年来材料领域研究的热点纤维材料,具有高强度、耐高温等良好的性能。纤维材料的性质依赖于自身的结构和组成,热分解过程对于研究材料的结构和热学性质有着十分重要的意义。热红联用技术做为一种新型的联用技术,既能定量又能定性地进行分析,在研究材料的热分解过程中具有明显的优势。由于Kevlar纤维的热分解过程在文献中少有报道,本文首次利用TG-FTIR联用技术对Kevlar纤维在室温到800 ℃的热解过程进行分析,得到了Kevlar纤维热解过程的详细步骤及各个步骤的反应产物。结果表明,Kevlar纤维的热解经历了3个阶段,分别为100～240,240～420,420～800 ℃。在500 ℃之前Kevlar纤维失重很缓慢,第三个阶段是纤维的主要失重阶段,最终固体的残留质量为56.21%。红外光谱数据表明,Kevlar纤维热解过程先释放出游离水,随后发生脱水反应和解聚反应,使纤维分子链断裂。最后纤维碎片进一步反应生成小分子气体,水、氨气、一氧化碳、二氧化碳为主要产物。其中水的析出量逐渐增大;氨气的析出量保持基本一致;一氧化碳仅在515～630 ℃产生,随后即氧化生成二氧化碳;二氧化碳的析出量经历了一个由于一氧化碳转化而产生的增长后,又下降到一定值保持稳定。     

Effect of air and oxygen content on the dielectric barrierdischarge decomposition of chlorobenzene

Experiments were performed on the plasma-assisted decomposition of dilute concentrations of chlorobenzene in air/oxygen and argon/oxygen gas mixtures at atmospheric pressure using a coaxial geometry single dielectric barrier discharge for different oxygen concentrations and energy densities. The results show that the decomposition process requires higher energy densities using air mixtures compared to argon/oxygen mixtures and is not linearly dependent on the oxygen content for a given energy density. The main decomposition products detected in the offgas were carbon dioxide and carbon monoxide     

Intumescent Flame Retardancy and Thermal Degradation of Epoxy Resin Filled with Ammonium Polyphosphate Using Thermogravimetric Analysis–Fourier Transform Infrared Spectroscopy and Thermogravimetric Analysis–Mass Spectrometry

The flammability of epoxy resin (EP) and its composite with ammonium polyphosphate (EPAPP) was investigated with limiting oxygen index (LOI), UL 94, and cone calorimeter tests. A systematic and comparative evaluation of the thermal degradation of EP and EPAPP has been investigated using thermogravimetry coupled with Fourier transform infrared spectroscopy (TG–FTIR) and thermogravimetry coupled with mass spectrometry (TG–MS). The results showed that the flame retardant of ammonium polyphosphate (APP) can constitute an intumescent flame retardant (IFR) system with EP, and APP can effectively improve the LOI of EP; with 6 wt% addition level of APP, EPAPP can pass UL 94 V 0 test. The cone calorimeter test results showed that the flame retardancy and smoke suppression of EP were significantly improved by APP, and toxic gas products such as carbon monoxide and carbon dioxide obviously decreased. Thermogravimetry–Fourier transform infrared spectroscopy and TG–MS results showed that the degradation process of EP produces large amounts of gas products and mainly containing of water, carbon dioxide, methane, benzene and its derivatives, as well as phenol and its derivatives. Compared to EP, the kinds of decomposition products of EPAPP sample were not changed significantly, except that more ammonia gas was generated. For the EPAPP sample, the products of water, benzene, and phenol increased, whereas the carbon dioxide and the flammable hydrocarbon fragments C_xH_y decreased significantly during the decomposition.     

Highly stretchable conductors comprising composites of silver nanowires and silver flakes

Journal of Nanoparticle Research - In this work, a process of thermal decomposition of metal carbonyls in oxygen-enriched supercritical carbon dioxide was studied. Manganese, iron, cobalt, and...     

Laser-induced decomposition of sodium azide

The decomposition of sodium azide, NaN₃, has been studied using a pulsed carbon dioxide laser. Chemiluminescence associated with the decomposition has been measured with and, without, the azide surface in the detector field of view. Near the decomposition threshold, emission has been observed in the wings of the Na 3p → 3s transition at 589 nm that has not been observed in previous azide decomposition experiments. This emission may be a result of surface reactions. Raman and visible absorption spectra have been obtained for the irradiated material; a new, as yet unidentified, band was observed in the Raman spectrum.     

Investigation of the photoelectronic properties of nanocrystalline carbon- and nitrogen-doped titanium dioxide

This paper reports the results of the study of photoelectronic properties of nanocrystalline titanium dioxide doped with carbon and nitrogen. Photo-generated paramagnetic radicals were detected and identified in nanocrystalline titanium dioxide by the electron paramagnetic-resonance method. The concentrations of the radicals versus the carbon and oxygen content were determined in the dark and under light exposure. The presence of C and CO ₂ ^? -radicals in carbon-doped titanium dioxide and mainly N and NO radicals in nitrogen-doped titanium dioxide is shown. The concentration of the radicals increases under light exposure, which indicates the recharging processes of electronic states in the bandgap, due to the presence of a dopant, accompanied by generation of paramagnetic particles. The electron paramagnetic resonance data correlate with the kinetics of formaldehyde decomposition on the titanium dioxide samples under study.     

Ion-exchange resin decomposition in supercritical water

Abstract

Using supercritical water oxidation, the cation exchange resin was decomposed fast and completely to water, carbon dioxide and sulfuric acid. While the resin decomposition yield increased with the reaction time and the amount of hydrogen peroxide added as oxidizing agent, it was constant in the resin concentration from 0.14 to 1.9 dry resin weight percent to water. More than 99% of the cation exchange resin was decomposed with hydrogen peroxide added in the amount of 7 times the stoichiometric value at 673 K and 30MPa for 30 minutes of the reaction time. The cation exchange resin is decomposed through two main reaction pathways. One has a rate controlling intermediate such as acetic acid whose decomposition rate was very slow, and the other does not have stable intermediates. The decomposition of the acetic acid is a significant factor for the complete decomposition of the resin, although it does not dominate the whole resin decomposition. A simple kinetic model that estimates the resin decomposition yield was developed.     

Effect of Annealing Treatment on Meta-poly(arylene sulfide sulfone amide)

A useful annealing treatment above glass transition temperature of high molecular weight amorphous m-poly(arylene sulfide sulfone amide) (m-PASSA) was employed in this work. No crystalline or cross-link structures were formed according to X-ray diffraction, differential scanning calorimetry, and nuclear magnetic resonance results; nevertheless, Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis results showed that the number of terminal carboxyl groups of annealed m-PASSA decreased after the annealing treatment. The volatiles formed in the decomposition of m-PASSA were investigated by combined thermogravimetric analysis and online FTIR. The initial volatile products in the decomposition experiments supported a process that involved the cleavage of an aromatic carboxyl group, followed by the emission of major volatile products—carbon dioxide, sulfur dioxide, and benzenthiol—released from the amide, sulfone, and diphenyl sulphide groups in m-PASSA. Annealed m-PASSA exhibited different thermal properties, as evidenced by thermogravimetric analysis, compared to the untreated polymer. The degradation activation energy increased from 154.4 kJ/mol to 173.6 kJ/mol after annealing treatment, and the lifetime was extended by more than 1000 times.     

Removal of carbon dioxide from gas mixtures by wollastonite

Wollastonite synthesis and decomposition were analyzed from the viewpoint of thermodynamics (using the TERRA software). It is shown that wollastonite synthesis from limestone and silica takes place at a minimum content of nitrogen (10^?5 N₂) with a release of carbon dioxide. The synthesis temperature is T ≥ 560 K. Wollastonite is decomposed in the presence of flue gas (4N₂) with limestone and silica formation and burial of carbon dioxide in the form of CaCO₃(c). Wollastonite decomposition temperature is T ≤ 420 K. The cyclic reciprocating process for complete removal of carbon dioxide by wollastonite is suggested. Four strokes of the reciprocating system with the fixed temperatures of wollastonite decomposition (T=300 K) and wollastonite synthesis (T=560 K) are presented. Total energy consumption (T = 560 K) is ΔI ≈ 130 kJ/mole, 30 % of energy is spent for heating and 70 % of energy is spent for chemical reaction. This is comparable with the heat of CO₂ solution in ethanolamin.     

Molecular beam studies of ethanol oxidation on Pd(110)

The adsorption and decomposition of ethanol on Pd(110) has been studied by use of a molecular beam reactor and temperature programmed desorption. It is found that the major pathway for ethanol decomposition occurs via a surface ethoxy to a methyl group, carbon monoxide and hydrogen adatoms. The methyl groups can either produce methane (which they do with a high selectivity for adsorption below 250 K) or can further decompose (which they do with a high selectivity for adsorption above 350 K) resulting in surface carbon. If adsorption occurs above 250 K a high temperature (450 K) hydrogen peak is observed in TPD, resulting from the decomposition of stable hydrocarbon fragments. A competing pathway also exists which involves C---O bond scission of the ethoxy, probably caused by a critical ensemble of palladium atoms at steps, defects or due to a local surface reconstruction. The presence of oxygen does not significantly alter the decomposition pathway above 250 K except that water and, above 380 K, carbon dioxide are produced by reaction of the oxygen adatoms with hydrogen adatoms and adsorbed carbon monoxide respectively. Below 250 K, some ethanol can form acetate which decomposes around 400 K to produce carbon dioxide and hydrogen.     

Propylene deep oxidation on the Pt(111) surface: temperature programmed studies over extended coverage ranges

Propylene oxidation was studied on the Pt(111) surface over a wide range of reaction stoichiometries using temperature programmed methods. Reaction of propylene with excess oxygen results in complete oxidation to water and carbon dioxide, with oxydehydrogenation to form water beginning at 290 K. The initiation of skeletal oxidation occurs after water formation begins, except for the highest propylene coverages. A stable dehydrogenated intermediate with a C₃H₅ stoichiometry is formed in the 300 K temperature range during oxidation. Reaction of propylene with substoichiometric amounts of oxygen results in incomplete oxidation with hydrocarbon decomposition dominating after depletion of surface oxygen. Increasing oxygen coverage results in more complete oxidation. Oxidation processes result in water, carbon dioxide, and carbon monoxide, while decomposition results in hydrogen, propylene, and propane desorption with some surface carbon remaining. Propylene-d₆ and selectively labeled propylene-3,3,3-d₃ (CH₂CHCD₃) experiments indicated initial water formation results from oxydehydrogenation of one of the olefinic hydrogens. At the highest propylene and oxygen coverages studied, we observed small amounts of partial oxidation which indicate that the vinyl hydrogen is removed initially, resulting in the formation of an adsorbed H₂CCCH₃ intermediate. The partial oxidation products observed are acetone desorbing at 200 K and acetic acid at 320 K. Removal of the first skeletal carbon begins at 320 K, except for the highest propylene coverages. Preadsorption of molecular oxygen limits adsorption of propylene and preadsorption of propylene limits molecular oxygen adsorption at 110 K. Similar oxidation mechanisms are observed following initial adsorption of both molecular and atomic oxygen, which is expected since molecular oxygen dissociates and/or desorbs well below oxidation temperatures.     

钾基CO2吸收剂再生反应特性

通过热重分析试验研究了钾基 CO2 吸收剂的再生反应特性.深入分析了气氛、分解终温和升温速率对再生转化率和分解反应速率的影响.通过热分析方法求取了反应动力学参数.研究发现,其分解终温最佳值为 200℃;CO2 和H2O 在分解终温较低时对反应过程的影响较大;升温速率对反应的影响程度在其高于 10℃/min 后明显减弱;KHCO3分解反应的表观活化能为 90～120 kJ/mol.本文为干法 K2CO3/KHCO3 循环脱除 CO2 的研究提供了一定的基础数据.     

Post-irradiation sensitization of CR-39 track detector in carbon dioxide atmosphere

The effect of post-irradiation treatment of CR-39 track detector in carbon dioxide atmosphere on the alpha particle registration sensitivity was investigated. Significant increase in etch rate ratio for 6.1 MeV ²⁵²Cf alpha particle was observed. The sensitization increasedboth as a function of trating time and as a function of carbon dioxide pressure in the treating vessel. Energy dependence of the sensitization was found to be small in the 2–9 MeV alpha particle energy interval. Fading of latent tracks after the sensitization process was slow in a one day period. Pre-irradiation treatment in carbon dioxide showed also some sensitization, though to a lesser extent than post-irradiation treatment. However, exposing CR-39 alpha particles in pure carbon dioxide atmosphere resulted in dramatic decrease in sensitivity. The role of dissolved oxygen and carbon dioxide in the primary latent track formation and in post-irradiation latent track transformation is discussed. Potential influence of the application of sensitization of CR-39 in radon, neutron and cosmic ray charged particle dosimetry is also discussed.     

直射太阳光红外吸收光谱技术遥测大气中二氧化碳柱浓度

大气中二氧化碳浓度持续增高导致环境和气候变化等问题成为人们关注的焦点. 为了实时遥测二氧化碳气体柱浓度, 研究了一种地基低分辨遥测系统和实时光谱数据反演分析方法. 利用该系统在合肥地区进行了连续观测, 从太阳吸收光谱中实时获取了整层大气透过率. 采用逐线积分非线性最小二乘光谱反演算法, 从整层大气透过率中反演了二氧化碳柱浓度和氧气柱浓度, 并以氧气柱浓度为内标函数获得了二氧化碳干空气柱体积混合比, 精密度优于3%. 将2012年9月25日12时到15时本系统测量的二氧化碳干空气柱体积混合比均值与此时段过境本站点区域的日本温室气体卫星观测结果进行了比较, 两者偏差小于1%.可见, 该系统和方法具有很高的精密度和准确度, 是一种有效的温室气体观测手段. 关键词： 红外吸收光谱技术 遥测 二氧化碳 柱浓度     

Structural and Parametric Optimization of S–CO2 Nuclear Power Plants

The transition to the use of supercritical carbon dioxide as a working fluid for power generation units will significantly reduce the equipment′s overall dimensions while increasing fuel efficiency and environmental safety. Structural and parametric optimization of S–CO₂ nuclear power plants was carried out to ensure the maximum efficiency of electricity production. Based on the results of mathematical modeling, it was found that the transition to a carbon dioxide working fluid for the nuclear power plant with the BREST–OD–300 reactor leads to an increase of efficiency from 39.8 to 43.1%. Nuclear power plant transition from the Rankine water cycle to the carbon dioxide Brayton cycle with recompression is reasonable at a working fluid temperature above 455 °C due to the carbon dioxide cycle′s more effective regeneration system.     

Gas forming processes within lignite mining dumps

Gas analyses of the soil atmosphere of lignite mining dumps yielded increased contents of carbon dioxide. To get information about the potential sources and the carbon dioxide releasing capacity of the dumps, samples of dump material were investigated for their contents and isotopic compositions of organic and inorganic carbon as well as the carbon dioxide in the soil atmosphere. The contents of organic and inorganic carbon were found to vary depending on type of dump material. The isotopic composition of the organic carbon ranges between -24.5 and -26.5 per thousand, which is typical for humous materials. The carbonates are found to be of marine origin (delta13C: +0.5 to -1.1 per thousand). By means of the isotope investigations it could be shown that the carbon dioxide in the lignite mining dump arises from these two different sources. Mixing ratios can be calculated using the isotope balance equation. Both reaction paths are associated with oxygen consumption and do not result in an increased gas pressure within the dump.     

A study of the gasification of carbon black with molten salt of Li2CO3 and K2CO3 for application in the external anode media of a direct carbon fuel cell

The characteristics of gasification reactions for carbon–carbonate mixtures were experimentally investigated at high temperatures up to 900 °C, considering the application of the mixtures to the external anode media of a direct carbon fuel cell. A thermo-gravimetric analysis (TGA) was conducted in either a nitrogen or carbon dioxide ambient environment for Li₂CO₃, K₂CO₃ and a mixture of these two substances with carbon black. Changes in the exit gas composition were also monitored during the heating process. It was shown that gasification in the mixture media occurs much more rapidly than carbonate decomposition at elevated temperatures, even for low concentrations of CO₂. It was also shown that the loading of carbonates to carbon significantly affects the global gasification reaction; it increased the reaction rate by an order of magnitude and decreased its activation energy. Based on the experimental observations, a simplified reaction model of gasification was suggested for the anode media of a DCFC, regarding carbonate-catalysed and metal-catalysed pathways of Boudouard reactions.     

基于可调谐多模二极管激光吸收光谱的二氧化碳浓度测量

可调谐二极管激光吸收光谱技术(TDLAS)具有高分辨率、高灵敏度和快速测量等特点,是气体探测中的主流技术。使用多模二极管激光器作为光源,将多模二极管激光吸收光谱技术与关联光谱技术相结合有助于提高测试可靠性和稳定性,同时还可有效解决单模二极管激光器长时间工作时中心波长随外界温度或机械特性的变化而发生偏移的问题。以1 570 nm多模二极管激光器为光源,利用多模二极管激光关联光谱和波长调制的气体测量技术(TMDL-COSPEC-WMS),通过计算待测气体和参考池气体之间二次谐波信号峰值高度之间的关系,实现了对二氧化碳浓度的测量。实验中二氧化碳浓度测量范围在0.6%～30%之间,计算结果表明,二氧化碳浓度与真实浓度值之间具有良好的线性关系,其线性度为0.998 7,线性拟合的斜率为1.061±0.016 8。对二氧化碳与氮气混合气体的连续测量结果表明,系统的探测极限达到335 ppm·m,对同一样品在20 min内的20次连续测量的标准偏差为0.036 7%,表明了系统良好的稳定性,所有测量结果都显示了系统用于二氧化碳气体监测的有效性。     

Gas Forming Processes within Lignite Mining Dumps

Abstract

Gas analyses of the soil atmosphere of lignite mining dumps yielded increased contents of carbon dioxide. To get information about the potential sources and the carbon dioxide releasing capacity of the dumps, samples of dump material were investigated for their contents and isotopic compositions of organic and inorganic carbon as well as the carbon dioxide in the soil atmosphere. The contents of organic and inorganic carbon were found to vary depending on type of dump material. The isotopic composition of the organic carbon ranges between ?24.5 and ?26.5‰, which is typical for humous materials. The carbonates are found to be of marine origin (δ¹³C: +0.5 to ?1.1‰). By means of the isotope investigations it could be shown that the carbon dioxide in the lignite mining dump arises from these two different sources. Mixing ratios can be calculated using the isotope balance equation. Both reaction paths are associated with oxygen consumption and do not result in an increased gas pressure within the dump.     

基于超窄带激光器扫描技术的气体检测研究

基于气体的差分吸收检测原理和超窄带半导体激光器的光谱扫描技术,设计了一种高精度分布式二氧化碳气体检测网络.系统采用超窄带可调谐半导体激光器作为光源,设计了新型气室结构,通过方波信号对光源光谱进行调制,消除了其他气体成分和灰尘颗粒的干扰,并结合空分复用技术,实现了二氧化碳的实时分布式检测.利用超窄带光谱扫描技术测得了不同...