中国化学品环境暴露评估领域的综合区划

大尺度空间（中国）化学品环境暴露多介质模型的建立需要先对空间做相应的区划.本文以ArcGIS软件为平台,通过有空间约束的聚类方法和水文分析方法相耦合,建立全国范围的综合分区.全国范围分为华南综合大区、华北综合大区、西北综合大区、华东综合大区、东北综合大区和西南综合大区6个综合大区.每个综合大区又分别包含了若干个综合小区,小区总数为38个.该研究为我国暴露评估的综合分区提供了一个方案,在多介质模型的建立中起着重要的作用.     

磁性有序介孔碳的制备及其对水中双酚A的吸附

采用水热法成功制备了磁性有序介孔碳（Fe-OMC）,用于吸附水中双酚A （BPA）.采用高倍投射电镜、X射线衍射仪、傅里叶红外光谱仪、比表面积分析仪和振动样品磁强计对Fe-OMC进行表征.结果表明,该吸附剂具备较大的比表面积、独特的有序介孔孔道结构、丰富的含氧官能团以及较强的超顺磁性.Fe-OMC能够高效地吸附去除水中的BPA,平衡吸附量可达72.62mg/g,经过外加磁场分离回收后依旧具备较好的吸附性能.随着BPA浓度从1mg/L提高到20mg/L,其平衡吸附量由8.33mg/g增至91.78mg/g.随着pH值的升高呈现出先降低后升高再降低的趋势,最高吸附量出现在pH=8（75.34mg/g）.Fe-OMC对BPA的吸附过程可用准二级吸附动力学模型和Langmuir吸附等温模型进行描述.计算的热力学参数表明,Fe-OMC对BPA的吸附过程是自发进行的放热过程.     

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。     

土地利用方式下土壤有机碳特征及影响因素——以后寨河喀斯特小流域为例

为研究喀斯特小流域土壤有机碳空间分布与土地利用之间的关系,基于网格法在后寨河流域挖掘了2 755个土壤剖面,并采集了22 057个土壤样品。分析了后寨河流域不同土地利用方式下土壤有机碳密度特征。结果表明：后寨河流域土壤有机碳密度主要受人为干扰、土壤厚度与岩石裸露率的制约。不同利用方式土壤有机碳密度（0~100 cm）总体上呈现以下规律：水田>旱地>经果林地>园地>草地>弃耕地>坡耕地>乔灌木林地>乔木林地>荒地>灌木林地>灌草地。后寨河流域100 cm土壤有机碳平均碳密度为8.70 kg/m²,低于中国土壤有机碳平均密度10.83 kg/m²,总有机碳储量为5.39×10⁸ kg。科学合理地进行土地利用方式调整与管理,可以增大喀斯特小流域土壤有机碳储量。     

提升汇流环湿热环境适应性方法研究

目的提高汇流环在湿热环境下的适应能力。方法实物解剖,观察汇流环绝缘材料损坏情况、碳粉堆积情况,在不同温度、湿度下测试绝缘材料绝缘度、抗电强度,碳粉堆积和导电情况,比对不同绝缘材料性能,并找出最适合的绝缘材料,比对滚动汇流环、碳刷组件、刷丝组件,找到解决碳粉堆积的方法。结果汇流环受湿热影响会从接缝处和电缆连接处进入湿气,温度、湿度的上升会使得原绝缘材料性能下降,长时间使用汇流环,碳粉会在汇流环内堆积并受到湿热的影响而导电,局部密封汇流环可以减少湿气进入。PPO材料性能优异,可以替换原绝缘材料从而减少湿热的影响,使用刷丝组件替代碳刷可以避免碳粉的产生。结论综合运用局部密封、绝缘材料改进、碳刷组件改进三种措施,可以有效提高汇流环在湿热环境下的适应能力。     

碳量子点掺杂氮化碳提高的光电化学阴极保护性能研究

目的研究g-C_3N_4/C-Dots-M复合材料的光电化学阴极保护性能。方法采用X射线衍射(XRD)、扫描电子显微镜(SEM)和紫外可见漫反射光谱技术对样品的晶体结构、微观形貌和光吸收性能进行表征。通过电化学测试可见光照射下g-C_3N_4/C-Dots-M复合材料光电极偶联316L不锈钢后的光电化学阴极保护电流密度和电位变化曲线,研究材料的光电化学阴极保护性能。结果可见光照射下,该偶联体系的光致混合电位下降至-0.43 V(vs. Ag/AgCl),光电化学阴极保护电流密度达到4.3μA/cm。结论得益于碳量子点优异的电子传导特性,g-C_3N_4/C-Dots-550复合材料的光电化学阴极保护性能比纯g-C_3N_4的明显增强。该复合材料在光电化学阴极保护方面展现了较大的应用潜力。     

包装箱用碳纤维增强复合材料贮存寿命研究

目的研究碳纤维增强复合材料贮存条件下的性能变化趋势和寿命评估。方法对碳纤维增强复合材料开展四个不同温度条件下的热氧老化试验,按试验周期定期取样开展冲击性能测试,对试验数据采用寿命预估方法进行处理,对材料性能进行预估。结果通过数据计算分别得到我国热带海洋、干热沙漠等典型气候条件下的碳纤维增强复合材料贮存寿命分别为17.21~35.89年。结论碳纤维增强复合材料具有较好的贮存性能,在较为严酷的热带海洋气候和给定的失效判据条件下,寿命预计为17.21年。试验和数据处理方法可以较好地预计材料的性能变化趋势和开展寿命评估。     

Factors influencing Aerosol Characteristics over Urban Environment

Atmospheric aerosols are an important contributing factor to turbidity in urban areas besides having impact on health. Aerosol characteristics show a high degree of variability in space and time as anthropogenic share of total aerosol loading is quite substantial and is essential to monitor the aerosol features over long time scales. In the present study extensive observations of columnar aerosol optical depth (AOD), total columnar ozone (TCO) and precipitable water content (PWC) have been carried over a tropical urban city of Hyderabad, India. Significant variations of AOD have been observed during course of the day with low values of AOD during morning and evening hours and high values during afternoon hours. Spectral variation of AOD exhibits high AOD at smaller wavelengths and vice versa except a slight enhancement in AOD at 500 nm. Anomalies in AOD, particulate matter and black carbon concentrations have been observed during May, 2003. Back trajectory analysis of air mass during these episodes suggested variation in air mass trajectories. Analysis of the results suggests that air trajectories from land region north of study area cause high loading of atmospheric aerosols. The results are discussed in the paper.     

Mega-Development Trends in the Amazon: Implications for Global Change

This paper describes four global-change phenomena that are having major impacts on Amazonian forests. The first is accelerating deforestation and logging. Despite recent government initiatives to slow forest loss, deforestation rates in Brazilian Amazonia have increased from 1.1 million ha yr^–1 in the early 1990s, to nearly 1.5 million ha yr^–1 from 1992–1994, and to more than 1.9 million ha yr^–1 from 1995–1998. Deforestation is also occurring rapidly in some other parts of the Amazon Basin, such as in Bolivia and Ecuador, while industrialized logging is increasing dramatically in the Guianas and central Amazonia.The second phenomenon is that patterns of forest loss and fragmentation are rapidly changing. In recent decades, large-scale deforestation has mainly occurred in the southern and eastern portions of the Amazon — in the Brazilian states of Pará, Maranho, Rondônia, Acre, and Mato Grosso, and in northern Bolivia. While rates of forest loss remain very high in these areas, the development of major new highways is providing direct conduits into the heart of the Amazon. If future trends follow past patterns, land-hungry settlers and loggers may largely bisect the forests of the Amazon Basin.The third phenomenon is that climatic variability is interacting with human land uses, creating additional impacts on forest ecosystems. The 1997/98 El Niño drought, for example, led to a major increase in forest burning, with wildfires raging out of control in the northern Amazonian state of Roraima and other locations. Logging operations, which create labyrinths of roads and tracks in forsts, are increasing fuel loads, desiccation and ignition sources in forest interiors. Forest fragmentation also increases fire susceptibility by creating dry, fire-prone forest edges.Finally, recent evidence suggests that intact Amazonian forests are a globally significant carbon sink, quite possibly caused by higher forest growth rates in response to increasing atmospheric CO₂ fertilization. Evidence for a carbon sink comes from long-term forest mensuration plots, from whole-forest studies of carbon flux and from investigations of atmospheric CO₂ and oxygen isotopes. Unfortunately, intact Amazonian forests are rapidly diminishing. Hence, not only is the destruction of these forests a major source of greenhouse gases, but it is reducing their intrinsic capacity to help buffer the rapid anthropogenic rise in CO₂.     

过氧化聚吡咯/聚乙烯吡咯烷酮修饰碳糊电极测定废水中苯酚

建立了过氧化聚吡咯(OPPy)和聚乙烯吡咯烷酮(PVP)修饰碳糊电极测定废水中苯酚的方法.优化了试验条件,苯酚的氧化峰电流在1.0×10-5 mol/L～1.0×10-3 mol/L之间线性关系良好,检出限为1.0×10-6 mol/L.该电极制作简单,选择性好,测定灵敏度高,精密度与准确度均符合要求.