基于锥形量热仪的计算机显示器燃烧特性分析

利用锥形量热仪对计算机显示器材料进行小尺寸燃烧性能试验研究,通过改变锥形量热仪的热辐射强度模拟中、小规模火灾。分析火灾中显示器样品的热释放速率(HRR)、质量损失速率、CO产生率和比消光系数。试验发现当热辐射强度为35 kW/m2时,计算机显示器的热释放速率比其在热辐射强度为75 kW/m2时多一个加速增长阶段,主要原因是在此热辐射强度下,材料热解速度缓慢,表面炭层厚度逐渐增厚,热量积聚后,材料热解速度增大,热释放速率加速达到第二个峰值;显示器材料在2种热辐射强度下的质量损失速率分3个阶段,炭层的包覆作用对其质量燃烧速率影响较小;显示器材料在燃烧过程中CO产生率、比消光系数和质量燃烧速率成线性递增关系。试验结果可反映显示器在真实火灾中的燃烧特性。     

Comparisons of TGA and DSC approaches to evaluate nitrocellulose thermal degradation energy and stabilizer efficiencies

This study investigated the thermal degradation energy (activation energy, E_a) for nitrocellulose (NC) with low nitrogen content of 11.71 mass%, so-called NC3, by using two different kinds of thermal analysis instruments: thermogravimetric analyzer (TGA) and differential scanning calorimetry (DSC). A comparison of E_a for various nitrogen content NC samples at two scanning rates (5 and 10 °C min^?1) tested by TGA and DSC is also discussed in this paper. Meanwhile, our aim was to analyze the anti-degradation of E_a for NC with high nitrogen content, as so-called NC1. Thermal stability for NC1 with diphenylamine (DPA) was tested via DSC with 10 DPA concentrations in weights of 0, 0.25, 0.50, 0.75, 1.0, 1.25, 1.50, 1.75, 2.0, and 3.0 mass%. Experimental results indicated that E_a of NC3s was 319.91 kJ mol^?1. Moreover, that while dosing DPA into NC1 the best recipe could be employed to avoid any violent NC1 runaway and also can be used to distinguish the differences of thermal decomposition E_a between NC with different nitrogen contents. This study established a fast and efficient procedure for thermal decomposition properties of NC, and could be applied as an intrinsically safer design during relevant operations.     

Reaction hazard and mechanism study of H2O2 oxidation of 2-butanol to methyl ethyl ketone using DSC,Phi-TEC II and GC-MS

Methyl ethyl ketone (MEK) oxidation via H₂O₂ with tungsten-based polyoxometalate catalysts has gained much attention with an ever-growing body of knowledge focusing on the development of environmentally benign processes in chemical industry. In this study, two calorimetry techniques, differential scanning calorimetry (DSC) and Phi-TEC II adiabatic calorimetry, were employed to analyze the thermal hazards associated with the 2-butanol oxidation reaction system. Hydrogen peroxide was the oxidant and a tungsten-based polyoxometalate as the catalyst. Gas chromatography-mass spectrometry was used for identification of the organic products. Important thermal kinetic data were obtained including “onset” temperature, heat of reaction, adiabatic temperature rise and self-heat rate. From DSC results, three exothermic peaks were detected with a total heat generation of approximately 1.26 kJ/g sufficiently to induce a thermal runaway. Possible reaction pathway for three stages were proposed based on both DSC and GC-MS results. One exotherm was detected by Phi-TEC II calorimeter and the pressure versus temperature profile together with the DSC and GC-MS data demonstrate the complexity of 2-butanol reaction system under both thermal screening and adiabatic conditions.     

纳米金修饰分子印迹聚合膜电极检测双酚A

以纳米金修饰玻碳电极为基础电极,以双酚A为模板分子,以邻氨基苯硫酚为聚合单体,采用循环伏安法电聚合制备分子印迹聚合膜,利用循环伏安和交流阻抗法研究电极的电化学特性。结果表明,双酚A在修饰电极表面的反应是一个受吸附控制的等电子、质子转移的不可逆反应。采用差分脉冲伏安法检测双酚A,线性范围为5. 0×10~(-6)mol/L～4. 0×10~(-4)mol/L,检出限为2. 3×10~(-7)mol/L。将该电极用于自来水和牛奶样品的测定,结果均为未检出,加标回收率分别为93. 5%和95. 4%,3次测定结果的RSD分别为4. 0%和5. 7%。     

新疆绿洲城市夏季农田区对流层NO_2垂直柱浓度特征分析

2014年夏季6~8月利用地基多轴差分吸收光谱仪(MAX DOAS)在新疆绿洲城市乌鲁木齐市三道坝镇、库尔勒市西尼尔镇及博乐市84团农田区观测的NO_2垂直柱浓度(VCD)数据,结合同期的气象数据分析了NO_2VCD的变化特征。研究表明:1NO_2气体的日变化规律在乌鲁木齐市和库尔勒市农田区呈波浪式多峰特征,博乐市农田区呈明显的双峰形式,且峰值除了库尔勒市在午后外,乌鲁木齐市和博乐市均出现在早晚时段;2新疆绿洲城市农田区在夏季6月(3.327×1015molec/cm~2)的NO_2VCD最高,其次是7月(2.002×1015molec/cm~2),最低是8月(1.656×1015molec/cm2);3NO_2VCD与气温、水汽压气象要素密切相关;由于城市间地势、格局的差异,库尔勒市的NO_2浓度与风速呈显著正相关,乌鲁木齐市、博乐市的NO_2浓度与风速相关性不显著。     

Screening of Cd tolerant genotypes and isolation of metallothionein genes in alfalfa (Medicago sativa L.)

In order to evaluate Cd tolerance in wide-ranging sources of alfalfa (Medicago sativa) and to identify Cd tolerant genotypes which may potentially be useful for restoring Cd-contaminated environments, thirty-six accessions of alfalfa were screened under hydroponic culture. Our results showed that the relative root growth rate varied from 0.48 to 1.0, which indicated that different alfalfa accessions had various responses to Cd stress. The candidate fragments derived from differentially expressed metallothionein (MT) genes were cloned from leaves of two Cd tolerant genotypes, YE and LZ. DNA sequence and the deduced protein sequence showed that MsMT2a and MsMT2b had high similarity to those in leguminous plants. DDRT-PCR analysis showed that MsMT2a expressed in both YE and LZ plants under control and Cd stress treatment, but MsMT2b only expressed under Cd stress treatment. This suggested that MsMT2a was universally expressed in leaves of alfalfa but expression of MsMT2b was Cadmium (Cd) inducible.     

Evaluation of Poly(ethylene-terephthalate) Products of Chemical Recycling by Differential Scanning Calorimetry

Poly (ethylene-terephthalate), (PET) bottles waste was chemically recycled by glycolysis and hydrolysis. The depolymerization processes were carried out in different time intervals from 5 to 360 min, in two different molar ratios of PET/EG, 1:5 and 1:18 and at different temperatures. The PET glycolysis leads to formation of bis(2-hydroxy-ethyl)terephthalate (BHET) monomer and PET oligomers with hydroxyl and carboxyl end groups while PET hydrolysis is followed by formation of monomers terephthalic acid (TPA) and ethylene glycol (EG). Fractions of monomers and oligomers were further characterized by FTIR spectroscopy and by differential scanning calorimetry (DSC). The results show that DSC is successful method to describe the different structures of oligomers formed during chemical recycling of PET.     

城市污水厂污水污泥的热值测定分析方法研究

建立热力学指标是污水生物处理过程热力学分析的基础工作,目前仍缺乏污水污泥化学能测试的标准方法。采用IKA C5000型自动热量计对某城市二级污水处理厂进水、出水、初沉污泥、剩余污泥、混合污泥和脱水污泥进行了热值测定,样品前处理采用103～105℃烘干获得干燥基,用苯甲酸进行加标回收。参照煤的发热量测定方法得到样品的高位热值。试验结果显示：出水干燥基的热值为05 kJ/g,进水干燥基的热值为4 kJ/g以上,各工艺段的污泥干燥基热值较高,基本都在12 kJ/g以上,接近右江褐煤水平。测定结果的标准偏差≤±0.452%,相对标准偏差≤±0.136%。通过同一批样品的元素分析及Dulong公式理论推算,发现2种方法可得到相似的结果。     

Thermal safety assessment for solid organic peroxides

The thermal hazards of dicumyl peroxide (DCP) and benzoyl peroxide (BPO), self-reactive chemicals are identified and characterized using high-pressuredifferential scanning calorimeter, and simultaneous thermogravimetric analyzer, a C80 micro-calorimeter is used. The apparent exothermic onset temperature of DCP is found to be between the range of 112–122 °C for different heating rates in DSC tests. There are two coupled peaks of BPO around 105 °C at both the heating rates of 4.0 and 8.0 °C/min while no endothermic peak showed at lower heating rates. Furthermore, another endothermic peak appears immediately after the exothermic peak at about 211 °C of DCP under high-pressure conditions. For BPO, the endothermic peak before the exothermic peak disappears as the pressure increases to 1.0 and 1.5 MPa. The average values of apparent activation energy calculated by Flynn-Wall-Ozawa and Kissinger-Akahira-Sunose methods during the conversion rate between 15 and 75% of DCP are 80.69 and 74.05 kJ/mol, and that of BPO are 119.96 and 112.93 kJ/mol, respectively. According to the isothermal tests, the thermal decomposition of DCP behaviors is an n-th order reaction while BPO conforms to the laws of autocatalytic reaction.     

Research on the critical temperature of thermal decomposition for large cartridge emulsion explosives

Emulsion explosives are one type of main industrial explosives. The emergence of the large cartridge emulsion explosives has brought new security incidents. The differential scanning calorimeter (DSC) and the accelerating rate calorimeter (ARC) were selected for the preliminary investigation of the thermal stability of emulsion explosives. The results showed that the initial thermal decomposition temperatures were in the range of 232–239 °C in nitrogen atmosphere (220–232 °C in oxygen atmosphere) in DSC measurements and 216 °C in ARC measurements. The slow cook-off experiments were carried out to investigate the critical temperature of the thermal decomposition (T_c) of the large cartridge emulsion explosives. The results indicated that the larger the diameter of the emulsion explosives, the smaller the T_c is. For the large cartridge emulsion explosives with diameter of 70 mm, the T_c was 170 °C at the heating rate of 3 °C h⁻¹. It is a dangerous temperature for the production of the large cartridge emulsion explosives and it should cause our attention.