Fe2O3-CeO2-Bi2O3/γ-Al2O3 catalyst in the catalytic wet air oxidation (CWAO) of cationic red GTL under mild reaction conditions

Fe₂O₃-CeO₂-Bi₂O₃/γ-Al₂O₃, an environmental friendly material, was investigated. The catalyst exhibited good catalytic performance in the CWAO of cationic red GTL. The apparent activation energy for the reaction was 79 kJ·mol⁻¹. HO₂· and O₂·⁻ appeared as the main reactive species in the reaction. The Fe₂O₃-CeO₂-Bi₂O₃/γ-Al₂O₃ catalyst, a novel environmental-friendly material, was used to investigate the catalytic wet air oxidation (CWAO) of cationic red GTL under mild operating conditions in a batch reactor. The catalyst was prepared by wet impregnation, and characterized by special surface area (BET measurement), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The Fe₂O₃-CeO₂-Bi₂O₃/γ-Al₂O₃ catalyst exhibited good catalytic activity and stability in the CWAO under atmosphere pressure. The effect of the reaction conditions (catalyst loading, degradation temperature, solution concentration and initial solution pH value) was studied. The result showed that the decolorization efficiency of cationic red GTL was improved with increasing the initial solution pH value and the degradation temperature. The apparent activation energy for the reaction was 79 kJ·mol⁻¹. Hydroperoxy radicals (HO₂·) and superoxide radicals (O₂⁻·) appeared as the main reactive species upon the CWAO of cationic red GTL.     

管道中氢气-空气爆轰的多级泄爆数值模拟研究

为了研究管道内氢气的爆燃转爆轰及其抑制过程,对单个障碍物管道中氢气-空气混合物燃爆过程以及多级泄爆进行了二维数值模拟。基于氢气-空气19步详细化学反应动力学机理,以及k-ε湍流模型、概率密度函数输运方程和同位网格SIMPLE算法,采用计算流体软件Fluent进行模拟。结果表明:密闭管道无泄爆时,在距点火端1.5 m左右爆燃转为爆轰;泄爆口的位置对管道内氢气-空气预混气体的爆炸参数有重要影响,泄爆口位于管道中部时,能降低管道内爆轰超压,泄爆效果较好;位于管道中部单个泄爆口泄爆时,有效降低爆轰超压,管道中部设置2个泄爆口时,能通过压力和混合气体的泄放将管道中已经发生的爆轰衰减为爆燃;当有3个泄爆口泄爆时,管道中没有发生爆轰,达到良好的泄爆效果。     

ACP1000冷却水管道采用超疏水表面湍流流动数值模拟

目的 探索超疏水表面对ACP1000冷却水管道内流体流动的减阻性能和潜在工程应用,对冷却水管道内的湍流流动进行数值模拟计算,研究具有超疏水表面内壁的冷却水圆管管道内湍流的流动特性。方法 对超疏水表面采用交替的气–液、液–固表面进行模拟,湍流流动采用二维轴对称方法进行数值模拟计算。结果 随着超疏水表面气液比的增大,冷却水圆管内湍流流动的摩擦阻力系数随之减小;随着超疏水表面气液比的增大,冷却水圆管内湍流流动的能量损失随之降低。结论 超疏水表面的应用能够优化ACP1000冷却系统冷却水管道的流动性能。此结果对于未来进一步优化核电站冷却水系统设计提供了理论基础。     

法国核电应力腐蚀问题对我国核电技术发展的启示

2022年,法国电力公司（EDF）大量核电机组因一回路管道应力腐蚀开裂（SCC）问题而停堆检修,对法国甚至欧洲的生产生活造成巨大影响。针对该事件,在总结国内外核反应堆类似失效案例及材料老化研究成果的基础上,对反应堆不锈钢部件的SCC问题的机理、影响因素、抑制措施开展了分析,并结合我国核电机组服役时间逐渐延长,材料老化、设备失效问题日益突出的现状,提出我国核电运维改进措施,如优化残余应力、加强监督和检查,研发更有效的无损检测技术等。同时,探讨了我国在反应堆材料老化研究方面的发展方向。     

基于监测数据的土壤源热泵系统设计优化分析

针对建筑中地源热泵系统实际地下换热过程复杂、设计困难等问题,以苏州地区某浅埋式地源热泵系统为研究对象,运用TRNSYS软件搭建地源热泵仿真模型,对一定条件下埋管内冷却水流速与地源热泵系统性能的耦合关系进行了模拟分析。仿真结果表明相同蓄热体积下埋管深度对系统性能影响较小。增大冷却水流速有利于土壤温度恢复,但系统耗电量增加。该浅埋式地源热泵系统冷却水流速1~2 m/s均在合理范围内,且埋管深度越大,最佳设计流速越小。     

实施注采一体管柱技术 节能降耗减污增效

超稠油蒸汽吞吐注采一体管柱技术,是对多项稠油开采工艺技术进行实践、总结、分析而来。该项技术,解决了作业频繁的问题,实现了不动管柱直接转抽,并可以多次注汽、转抽;由此而改变传统的蒸汽吞吐注采工艺技术,做到注、采、焖、放一体管柱,减少作业工序和降低井筒热损失,降低环境污染及电能消耗,实现超稠油不动管柱开采,有效降低超稠油开采成本,提高了油井的生产实效,并取得可观的经济效益和环境效益,实现节能、降耗、减污、增效的清洁生产目标。     

污水管网中无机氮类营养盐迁变规律

以一套长1 200 m的城市污水模拟管网为对象,采用人工配水方式,研究了管网中含氮化合物的变化情况,分析评价了沿程氮类营养盐的迁变转化特性.结果表明,以氯化铵为氮源基质,管网微生物将其同化合成生命所需的物质以进行细胞增殖.游离氨基酸、结合氨基酸、核酸是代谢产生的主要含氮有机化合物,其中氨基酸占溶解性有机氮(DON)的绝大多数.同时利用三维荧光光谱、尺寸排阻色谱技术对水中有机物的荧光特性及相对分子质量分布的表征结果显示,污水中有机物的特征荧光峰有所增多,主要以类蛋白、类微生物代谢产物为主,且荧光强度随管网沿程逐渐增强;水中的小分子营养盐在微生物的同化作用下转化为复杂的大分子有机物.     

Effects of dissolved oxygen and iron aging on the reduction of trichloronitromethane, trichloracetonitrile, and trichloropropanone

Iron metal (Fe(0)) is a potent reductant capable of reducing a wide variety of halogenated organic compounds including disinfection byproducts (DBPs). These reduction reactions may play a role in DBP fate in iron water mains and potentially could be exploited to remove DBPs from drinking water or wastewater in a packed-bed configuration. Oxidants (i.e., dissolved oxygen (DO) and chlorine) present in the water, however, may decrease the DBP degradation rate by competing for reactive sites and rapidly aging or corroding the iron surface. Thus, batch experiments were performed to investigate the effect of DO on the degradation rates of selected DBPs by Fe(0). Experiments were performed under anaerobic conditions, in initially oxygen saturated buffer without DO control, and under controlled DO (approximately 4.0 or 8.0 mg l⁻¹) conditions. The effect of short-term (25–105 min) iron aging in DO-containing buffer on DBP degradation rate also was investigated in separate experiments. For fresh Fe(0), the degradation rates of trichloronitromethane (TCNM) and trichloroacetonitrile (TCAN) in initially oxygen saturated buffer were similar to their respective rates under anaerobic conditions. The degradation rate of 1,1,1-trichloropropanone (1,1,1-TCP), however, decreased significantly in the presence of DO and the effect was proportional to DO concentration in the controlled DO experiments. For a DO concentration of 4 mg l⁻¹, the degradation rate of the three DBPs was greater for longer aging times as compared to their respective rates after 25 min, suggesting the formation of a mineral phase that increased reactivity. For a DO concentration of 8 mg l⁻¹, the effects of increasing aging time were mixed. TCNM degradation rates were stable for all aging times and comparable to that under anaerobic conditions. The TCAN and 1,1,1-TCP degradation rates, however, tended to decrease with increasing aging time. These results suggest that the reduction of highly reactive DBPs by Fe(0) will not be affected by the presence of DO but that the reaction rates will be slowed by DO for DBPs with slower degradation kinetics.     

零价铁与过硫酸盐异相芬顿降解活性艳橙X-GN

采用零价铁(Fe~0)与过硫酸盐构建异相类芬顿体系,由Fe0腐蚀释放Fe~(2+)催化S_2 O_8~(2-)产生硫酸根自由基快速降解偶氮染料活性艳橙,考察了初始p H值、Fe~0投加量、过硫酸盐投加量和温度对降解过程的影响。结果表明,当活性艳橙初始浓度为100 mg/L、pH值为7、Fe~0投加量为0.5 g/L、过硫酸盐投加量为1 mmol/L和反应温度为30℃时,反应60 min后活性艳橙降解率达到92.6%。酸性条件和提高反应温度均有利反应的进行,而且活性艳橙的降解率在初始pH值为9时也高于90%。反应过程符合准一级动力学,表观反应速率常数k为0.0513 min~(-1)(30℃)。UV-Vis扫描显示,活性艳橙的发色基团在反应过程中被破坏。由Fe~0与S_2O_8~(2-)构成的异相Fenton体系可作为一种高效手段用于染料废水的处理。     

Mercury mass flow in iron and steel production process and its implications for mercury emission control

The iron and steel production process is one of the predominant anthropogenic sources of atmospheric mercury emissions worldwide. In this study, field tests were conducted to study mercury emission characteristics and mass flows at two iron and steel plants in China. It was found that low-sulfur flue gas from sintering machines could contribute up to41% of the total atmospheric mercury emissions, and desulfurization devices could remarkably help reduce the emissions. Coal gas burning accounted for 17%–49% of the total mercury emissions, and therefore the mercury control of coal gas burning, specifically for the power plant burning coal gas to generate electricity, was significantly important. The emissions from limestone and dolomite production and electric furnaces can contribute29.3% and 4.2% of the total mercury emissions from iron and steel production. More attention should be paid to mercury emissions from these two processes. Blast furnace dust accounted for 27%–36% of the total mercury output for the whole iron and steel production process. The recycling of blast furnace dust could greatly increase the atmospheric mercury emissions and should not be conducted. The mercury emission factors for the coke oven,sintering machine and blast furnace were 0.039–0.047 g Hg/ton steel, and for the electric furnace it was 0.021 g Hg/ton steel. The predominant emission species was oxidized mercury, accounting for 59%–73% of total mercury emissions to air.