Coupling mechanism of activated carbon mixed with dust for flue gas desulfurization and denitrification

To clarify the effect of coking dust, sintering dust and fly ash on the activity of activated carbon for various industrial flue gas desulfurization and denitrification, the coupling mechanism of the mixed activated carbon and dust was investigated to provide theoretical reference for the stable operation. The results show that coking dust had 34% desulfurization efficiency and 10% denitrification efficiency; correspondingly, sintering dust and fly ash had no obvious desulfurization and denitrification activities. For the mixture of activated carbon and dust, the coking dust reduced the desulfurization and denitrification efficiencies by blocking the pores of activated carbon, and its inhibiting effect on activated carbon was larger than its own desulfurization and denitrification activity. The sintering dust also reduced the desulfurization efficiency on the activated carbon while enhancing the denitrification efficiency. Fly ash blocked the pores of activated carbon and reduced its reaction activity. The reaction activity of coking dust mainly came from the surface functional groups, similar to that of activated carbon. The reaction activity of sintering dust mainly came from the oxidative property of Fe₂O₃, which oxidized NO to NO₂ and promoted the fast selectively catalytic reduction (SCR) of NO to form N₂. Sintering dust was activated by the joint action of activated carbon, and both had a coupling function. Sintering dust enhanced the adsorption and oxidation of NO, and activated carbon further promoted the reduction of NO_x by NH₃; thus, the denitrification efficiency increased by 5%-7% on the activated carbon.     

Metabolomic modulations in a freshwater microbial community exposed to the fungicide azoxystrobin

An effective broad-spectrum fungicide, azoxystrobin (AZ), has been widely detected in aquatic ecosystems, potentially affecting the growth of aquatic microorganisms. In the present study, the eukaryotic alga Monoraphidium sp. and the cyanobacterium Pseudanabaena sp. were exposed to AZ for 7 days. Our results showed that 0.2–0.5 mg/L concentrations of AZ slightly inhibited the growth of Monoraphidium sp. but stimulated Pseudanabaena sp. growth. Meanwhile, AZ treatment effectively increased the secretion of total organic carbon (TOC) in the culture media of the two species, and this phenomenon was also found in a freshwater microcosm experiment (containing the natural microbial community). We attempted to assess the effect of AZ on the function of aquatic microbial communities through metabolomic analysis and further explore the potential risks of this compound. The metabonomic profiles of the microcosm indicated that the most varied metabolites after AZ treatment were related to the citrate cycle (TCA), fatty acid biosynthesis and purine metabolism. We thereby inferred that the microbial community increased extracellular secretions by adjusting metabolic pathways, which might be a stress response to reduce AZ toxicity. Our results provide an important theoretical basis for further study of fungicide stress responses in aquatic microcosm microbial communities, as well as a good start for further explorations of AZ detoxification mechanisms, which will be valuable for the evaluation of AZ environmental risk.     

基于最大熵模型的福建省红树林潜在适生区评估

本研究利用生物气候、地形、底质类型、海温等环境因子和红树林分布数据建立了福建省红树林分布模型,基于最大熵方法分析了福建省沿岸红树林潜在适生区的空间分布.根据模型输出结果对福建省红树林的生境适宜性进行了评估,识别了影响红树林分布的关键环境因子及其适生值区间,并通过空间叠加分析获取了福建省红树林保护与修复的优先区与空缺区域.结果表明,影响福建省红树林适生区分布格局的主要环境因子包括海表温度、气温和降水等,福建省红树林潜在适生区主要位于沙埕港-三沙湾-兴化湾沿岸、泉州湾-厦门湾-九龙江口沿岸、漳江口-东山湾沿岸等地,其中最优适生区面积约为91km².全省共识别出8处红树林保护与修复的优先区域,现存红树林保护率约为64.4%,保护修复空缺主要出现在沙埕港、三沙湾、罗源湾、福清湾等处,研究结论可为未来福建省红树林保护和修复行动提供科学参考.     

Well-to-wheels greenhouse gas and air pollutant emissions from battery electric vehicles in China

Mitigation and Adaptation Strategies for Global Change - Electric vehicles (EVs) play a crucial role in addressing climate change and urban air quality concerns. China has emerged as the global...     

机载产品盐雾试验结果评定判据分析与探讨

针对当前机载产品盐雾试验标准中缺少明确、可量化评估指标,试验结果评定判据粗略笼统且以定性评价为主,已不能满足产品发展和使用环境扩展需求等现状,在总结国内外现行盐雾试验标准的结果评定要求基础上,分析当前机载产品盐雾结果评定判据存在的问题与不足,从管理和技术两个层面提出改进试验结果评定可操作性的建议,指导机载产品盐雾试验实施与评价。     

石英灯辐射加热条件下低密度碳/酚醛复合材料高温响应及分析

目的研究低密度碳/酚醛复合材料在不同地面加热实验测试响应的差异性,指导材料在实际应用环境下的高温响应分析。方法对低密度碳/酚醛复合材料开展了热流为400 kW/m~2的单侧石英灯辐射加热实验,利用热电偶测温系统测量试件在加热过程中不同位置的温度时间历程,并对试件的烧蚀形貌和微观结构进行观测。同时与热流为464k W/m~2的氧乙炔加热陶瓷板辐射加热实验结果进行对比分析,并且采用有限元方法对材料的传热传质多场耦合计算进行分析。结果对于石英灯辐射加热,在测量点升温到接近200℃时,温度响应拐点都依次出现。由于加热的辐射热源不同,在不同的辐射波段下,多孔材料吸收和发射的热量不同,短时间内氧乙炔加热陶瓷板辐射加热使材料内部升温速率比石英灯辐射加热实验的要快,但长时间加热时现象刚好相反。结论进行传热传质多场耦合计算材料高温响应时,合理确定材料宏观性能随温度的变化至关重要。     

纤维增强气凝胶复合材料高温结构转变及热稳定性研究

目的研究高温受热条件下纳米复合隔热材料的结构转变特征及热稳定性。方法采用扫描电镜、X射线衍射仪、红外光谱仪及热重仪等检测方法。结果纤维增强气凝胶材料从室温到650℃存在连续的质量损失,从室温到放热前,质量损失为1.66%;365℃开始出现放热,温度升至398℃时达到峰值,整个放热过程对应质量损失约为1.3%;从435℃放热结束开始到650℃的质量损失为1.46%。经过400℃热处理后,试样比表面积从268m~2/g增加到437m~2/g;当试样热处理温度达到600℃时,试样的比表面积明显随之降低至198m~2/g。结论 SiO_2气凝胶复合材料以无定形结构为主,存在少量的二氧化钛晶体。在400℃左右,SiO_2气凝胶结构中硅甲基Si—CH_3发生氧化,产生明显的放热峰,之后硅羟基Si—OH之间发生缩聚反应,使600℃热处理后气凝胶中Si—O—Si网络骨架强度有所提高。未处理的纤维增强气凝胶材料试样上气凝胶纳米颗粒构成的块体较为良好地包裹在玻璃纤维表面,而经过600℃的高温热处理1 h后,块体气凝胶脱离了光滑的纤维表面,气凝胶纳米粒子发生收缩,致使材料比表面积下降。     

油气田在役管道高后果区识别与完整性评价方法

根据油气管道建设与管理的相关标准与规范或导则,针对目前油气田在役管道,明确了其高后果区识别的划分及其在不同标准中的差异以及识别的原则和时间间隔,分别介绍了在管道的相关数据采集的基础上开展地质灾害和第三方破坏造成的管道风险评价方法,管道内外腐蚀的直接评价以及包括剩余强度、剩余寿命和材料在内的管道适用性评价方法,同时给出了这些评价工作所涉及到的相关内容项,对油田管道的完整性管理具有重要的指导作用和应用价值。     

纳米涂层/铝合金在不同pH值的海水溶液中的腐蚀行为研究

目的评价纳米涂层/铝合金在不同pH值海水溶液中的腐蚀行为。方法通过测试纳米涂层/铝合金试样在不同pH值海水溶液中的EIS值,分析试样阻抗谱图及Bode谱图的演化规律,建立不同EIS图谱的不同电极阻抗模型,并采用ZView软件解析涂层体系不同时期的电化学阻抗谱,获得涂层电阻的变化趋势,及不同pH值海水浸泡的纳米涂层体系腐蚀失效速度。结果随着浸泡时间的增加及pH值的降低,纳米涂层/铝合金体系腐蚀损伤失效速率在浸泡前期整体趋势增大,但中后期由于腐蚀产物逐渐堵塞了涂层的微孔,腐蚀介质向铝合金表面渗透的速率逐渐减小。结论 pH为2.0海水浸泡下的3涂层失效最快,其次是pH为4.0海水浸泡下的2涂层,最后为p H为6.0海水浸泡下的1涂层,该涂层体系应采用等效电路模型C进行拟合。     

未来气候变化对武夷山自然保护区毛竹异戊二烯排放速率的影响

采用全球气候模式Nor ESM1-M产生的RCP2.6、RCP4.5、RCP6.0和RCP8.5气候变化情景数据和植物异戊二烯排放计算模型,模拟分析了未来气候变化对武夷山自然保护区毛竹(Phyllostachys pubescens)异戊二烯排放速率的影响.结果显示,气候变化下武夷山自然保护区气温上升,年降水量和辐射强度波动较大,呈增加或下降趋势.毛竹异戊二烯平均日排放速率在未来气候变化情景下比基准情景下高约30μg·g~(-1)·d~(-1),在RCP8.5情景下比基准情景下高约48μg·g~(-1)·d~(-1);毛竹异戊二烯日排放速率在未来气候变化情景与基准情景下的差异在1~90 d和301~365 d较小,在91~300 d差异较大;相比基准情景,未来气候变化情景下毛竹异戊二烯日排放速率在1~190 d(平均增加15%以上)和271~365 d(平均增加20%)增幅较大,在191~270 d增幅较小,在RCP8.5情景下增幅最大(平均增加17%).另外,毛竹异戊二烯年排放速率在未来气候变化情景下比基准情景下约高10000μg·g~(-1)·a~(-1)以上,在RCP8.5情景下比基准情景下约高13%.研究表明,未来气候变化将使毛竹异戊二烯排放速率增加.