受限空间油气爆燃火焰形态

通过受限空间油气爆燃可视化实验发现，在不同初始油气体积分数下，爆燃火焰呈现出不同的表观特征，据此提出了受限空间油气爆燃的3种火焰形态，即光滑球形火焰、褶皱球形火焰和卷曲絮状火焰。分析了3种火焰形态的形成机理，并通过实验观测与理论分析，给出了区分3种火焰形态的临界条件。结合实验中采集到的关键参数，总结了不同的火焰形态下受限空间油气爆燃的反应产物、最大压力、升压速率、反应时间、火焰强度等关键参数的特征与变化规律。     

An analysis of peak overpressures in vented gaseous explosions

Experimental data from vented explosion tests using stoichiometric methane–air and 18% hydrogen–air mixtures in a 63.7 m³ chamber with a 2.7 or 5.4 m² vent are presented. Results from experiments conducted using stoichiometric propane–air in 2.42 m³ vessel with a 0.26 m² vent are also reported. The tests were focused on the effect of fuel, enclosure size, ignition location, vent size, and obstacles on the pressure development of a propagating flame in a vented enclosure. The dependence of the maximum pressure generated on the experimental parameters was analyzed. It was found that the pressure maxima may be caused by pressure transients controlled by the interplay of the maximum-flame area, the burning velocity, and the overpressure generated by an external explosion. A simple model was proposed to estimate the maximum pressure for each of the main pressure transients. The model was found to agree with the experimental data within the experimental uncertainty.     

蒸汽活化生物质焦吸附模拟烟气中SO2和NO的研究

以麦秆和稻壳生物质为研究对象,在不同的热解温度、热解速率以及蒸汽活化温度条件下制备了生物质焦,采用比表面积与孔隙度分析仪测定生物质焦的比表面积和孔隙结构参数。利用固定床吸附装置,研究了热解温度、热解速率、活化温度和模拟烟气中SO₂和NO浓度等因素对生物质焦吸附SO₂和NO性能的影响。结果表明,蒸汽活化可以显著提高生物质焦的BET比表面积、D-R比表面积、D-R微孔容积和总孔容,降低其平均孔径,并显著增加蒸汽活化生物质焦对SO₂与NO吸附的起始穿透时间和吸附量。快速热解下制得的蒸汽活化焦对SO₂和NO的吸附效果优于慢速热解,热解温度为873 K的蒸汽活化焦的吸附性能明显好于热解温度为673与1 073 K的蒸汽活化焦。在973~1 173 K下,随着蒸汽活化温度的提高,蒸汽活化生物质焦对SO₂和NO的吸附量呈现先上升后下降的趋势。随着模拟烟气中SO₂与NO浓度的降低,蒸汽活化生物质焦对SO₂与NO吸附的起始穿透时间延长,但相应的SO₂和NO吸附量下降。在873 K、快速热解和1 073 K条件下制得的蒸汽活化麦秆焦对SO₂和NO吸附量最大,其值分别为109.02和21.77 mg/g。     

稀释蒸汽中Na+及积炭对甲醇制丙烯催化剂性能影响

考察了稀释蒸汽中Na⁺及积炭对甲醇制丙烯(MTP)催化剂物理化学性质和催化性能影响, 及离子交换后催化性能. 采用X射线衍射(XRD)、扫描电镜(SEM)、X射线荧光(XRF)光谱、N₂吸附-脱附、程序升温氨脱附(NH3-TPD)和热重(TG)分析等方法对失活和再生催化剂进行了表征, 并在101325 Pa、470℃ 和甲醇空速(WHSV)为1.0-3.0 h^-1的反应条件下, 采用连续流动固定床微型反应器考察其催化甲醇制丙烯性能. 结果表明: MTP反应970 h后的催化剂晶体结构和形貌没有受到明显破坏, 但稀释蒸汽中Na⁺极易扩散至催化剂表面,部分取代H质子的位置, 从而使催化剂酸性逐渐下降而中毒失活; 另外, MTP催化剂表面的积炭导致分子筛微孔堵塞是造成其失活的主要原因, 可通过烧炭再生过程消除, 而水蒸汽脱铝对催化剂性能的影响缓慢但更严重. 用再生和离子交换处理后, Na⁺中毒催化剂MTP反应性能基本完全恢复. 在470 h反应过程中, 甲醇转化率保持在99%以上, 丙烯选择性大于46%, 且随着反应时间的延长, 丙烯选择性逐渐升高、乙烯选择性逐渐下降.     

2,2,2-三硝基乙基-N-硝基甲胺的热安全性

为评价2,2,2-三硝基乙基-N-硝基甲胺(TNMA)的热安全性, 得到计算TNMA热安全性参数用的基本数据, 用经验式估算了TNMA的比热容(C_p)和热导率(λ). 用键能贡献于生成热Q_f的加和法, 估算了TNMA的标准生成焓Δ_cH_m^θ(TNMA, s, 298.15 K). 用热力学公式计算了TNMA的标准燃烧焓ΔU_m^θ(TNMA, s, 298.15 K)和标准燃烧能Δ_cH_m^θ(TNMA, s, 298.15 K). 用Kamlet-Jacobs 公式估算了爆速、爆压和爆热. 用经验式估算了分解热(Q_d). 通过差示扫描量热(DSC)曲线和高灵敏度布鲁顿玻璃薄膜压力计测得的逸出气体标准体积(V_H)-时间(t)曲线, 得到了TNMA放热分解反应的动力学参数. 用上述基本数据得到了评价TNMA的热安全性参数: 自加速分解温度(T_SADT), 热爆炸临界温度(T_be0和T_bp0), 绝热至爆时间(t_TIad), 撞击感度50%落高(H₅₀), 热点起爆临界温度(T_cr), 被300 K环境包围的半厚和半径为1 m的无限大平板、无限长圆柱和球形TNMA的热感度概率密度函数S(T), 相应于S(T)-T关系曲线最大值的峰温(T_S(T)max), 安全度(SD), 临界热爆炸环境温度(T_acr)和热爆炸概率(P_TE). 结果表明: (1) TNMA有较好的热安全性和对热抵抗能力, 与环三亚甲基三硝胺(RDX)相比, TNMA易从热分解过渡到热爆炸; (2) 不同形状大药量TNMA 热安全性降低的次序为: 球>无限长圆柱>无限大平板; (3)TNMA有高的燃烧能、高的爆轰化学能(爆热)和接近环四亚甲基四硝胺(HMX)的爆炸性能, 其对冲击敏感, 冲击感度与季戊四醇四硝酸酯(PETN)和特屈尔接近, 可用作混合炸药主组分.     

The effect of copper content on the reactivity of Cu/Co6Al2 solids in the catalytic steam reforming of methane reaction

The steam reforming of methane over Cu/Co₆Al₂ mixed oxides with different copper contents was studied. The Co₆Al₂ support was prepared via the hydrotalcite route. It was thermally stabilized at 500 °C, impregnated with 5 wt.%, 15 wt.% or 25 wt.% copper using copper (II) nitrate Cu(NO₃)₂·3H₂O precursor and then calcined again at 500 °C under an air flow. The impregnation of copper enhanced significantly the reactivity of the solids in the considered reaction. The 5Cu/Co₆Al₂ solid was the most reactive one, with a methane conversion of 96% at 650 °C. The selectivities of H₂ and CO₂ were also better for the catalyst containing 5 wt.% copper compared to higher copper loadings. The decrease in the catalytic reactivity with increasing the copper content was attributed to the formation of agglomerated and less reactive CuO species, which were detected by XRD and TPR analyses.     

The Influence of Different Pretreatment Methods on Color and Pigment Change in Beetroot Products

Vegetable processing pomace contains valuable substances such as natural colors that can be reused as functional ingredients. Due to a large amount of water, they are an unstable material. The aim of our research was to assess how the pretreatment method (thermal or nonthermal) affects the properties of powders obtained from beet juice and pomace after the freeze-drying process. The raw material was steamed or sonicated for 10 or 15 min, and then squeezed into juice and pomace. Both squeezed products were freeze-dried. The content of dry substance; L*, a*, and b* color parameters; and the content of betalain pigments were analyzed. Pretreatments increased the proportion of red and yellow in the juices. Steam and ultrasound caused a significant reduction in parameter b* in the dried pomace. A significant increase in betanin in lyophilizates was observed after pretreatment with ultrasound and steam for 15 min. As a result of all experiments, dried juices and pomaces can also be used as a colorant source. However, there is higher potential with pomaces due to their additional internal substances as well as better storage properties. After a few hours, juice was sticky and not ready to use.     

基于Ti3C2-MXene的太阳能界面水汽转换

水资源匮乏是现代化发展中面临的全球性问题,太阳能界面水汽转换(Interfacial Solar Steam Generation, ISSG)是一种高效、绿色、低成本进行海水淡化和废水处理的方法。ISSG使用绿色的太阳能作为热源,通过光热转换并将热限制在水气界面上以高效产生蒸气,然后经过冷凝收集获得清洁水。设计和构筑具有强光吸收的光热转换材料是ISSG的技术核心。Ti₃C₂-MXene是一种新型二维碳化钛材料,具有比表面积大、水分散性好和光热转换效率高等优点,在ISSG领域具有巨大的应用潜力。本文介绍了ISSG技术和MXene,总结了光热转换材料的设计原则,论述了Ti₃C₂-MXene复合材料在ISSG领域的研究进展,其中包括二维MXene薄膜、三维MXene气凝胶和水凝胶、生物基-MXene复合材料的构筑和性能等,并分析了Ti₃C₂-MXene所面临的挑战和发展前景。     

物理化学教学中安全工程教育的融合与内化实例*

如何强化安全工程教育是化学化工类专业高等教育的一个重要课题。通过对蒸汽锅炉爆炸、火灾爆燃事故以及锈蚀危害等3个实例的详细讲述,指出在物理化学的教学中,若适时融入相关的安全工程教育,可以使学生深刻理解安全事故发生及防范所依赖的物理化学原理,从而起到安全意识的内化作用。教学中现代教育技术的引入可以增强这一效果。