分子印迹硅纳米改性氧化石墨烯复合材料的制备及其对双酚A的吸附研究

制备了分子印迹硅纳米-氧化石墨烯复合吸附材料,并研究了复合材料对双酚A(Bisphenol A,BPA)的吸附性能。实验结果表明:复合吸附材料对BPA的吸附在35min内达到吸附平衡,Langmuir等温线模型得出最大吸附容量约为338.3mg/g;相对于BPA的结构类似物,对BPA具有良好的选择吸附性能;在溶液p H接近6时对BPA的去除率最高,低温条件有利于吸附的进行;该材料具有优异的循环吸附性能。     

Packed in-tube solid phase microextraction with graphene oxide supported on aminopropyl silica: Determination of target triazines in water samples

On-line in-tube solid phase microextraction (in-tube SPME) coupled to high performance liquid chromatography and tandem mass spectrometry (HPLC-MS/MS) was successfully applied to the determination of selected triazines in water samples. The method based on the employment of a packed column containing graphene oxide (GO) supported on aminopropyl silica (Si) showed that the extraction phase has a high potential for triazines extraction aiming to its physical-chemical properties including ultrahigh specific surface area, good mechanical and thermal stability and high fracture strength. Injection volume and loading time were both investigated and optimized. The method validation using Si-GO to extract and concentrate the analytes showed satisfactory results, good sensitivity, good linearity (0.2–4.0 µg L^?1) and low detection limits (1.1–2.9 ng L^?1). The high extraction efficiency was determined with enrichment factors ranging from 1.2–2.9 for the lowest level, 1.3–4.9 intermediate level and 1.2–3.0 highest level (n = 3). Although the analytes were not detected in the real samples evaluated, the method has demonstrated to be efficient through its application in the analysis of spiked triazines in ground and mineral water samples.     

石墨烯薄膜原子氧剥蚀行为及电阻特性

目的研究石墨烯薄膜在原子氧空间环境的适应性,为其在航天器上应用提供参考。方法采用刮涂法制备石墨烯薄膜,将石墨烯薄膜材料及石墨烯电阻传感器置于微波源原子氧设备内开展原子氧试验,原子氧剂量分别为3.0×10^20 atoms/cm2和7.5×10^20 atoms/cm^2,研究薄膜表面形貌、结构、成分及电阻性能的变化。结果采用刮涂法可制备氧含量较低的石墨烯薄膜,原子氧剂量为7.5×10^20 atoms/cm^2情况下,石墨烯薄膜的厚度损失为5.3μm,原子氧反应率为7.14×10^-25 atoms/cm^3。原子氧作用后,石墨烯薄膜中碳原子无序程度增大,C—O、—COOH官能团含量降低,C=O官能团含量增加。石墨烯电阻传感器的R0/R比值随原子氧剂量增加线性降低,0.8μm厚度薄膜可探测最大原子氧剂量为5×10^19 atoms/cm^2,增加薄膜厚度有望提高传感器的使用寿命。结论得到了石墨烯薄膜厚度损失、原子氧反应率、微观结构及电阻特性的变化规律,可为石墨烯薄膜的空间应用提供技术支撑。     

Quantum dots enhance Cu2+-induced hepatic L02 cells toxicity

As a new class of xenogenous nanoparticle,quantum dots (QDs) possess the potential to co-exist with Cu2+ in human liver.The combined toxicity is thus concerned.Considering QDs and Cu2+ are known ROS (reactive oxygen species) inducer,we investigated the combined oxidative stress and corresponding protective strategy using human hepatic L02 cells.The results demonstrated that the presence of a small amount of MPA-CdTe QDs (2 μg/mL) in a Cu2+ solution (2.5-20 μg/mL) resulted in a higher toxicity with up to 8-fold cell viability decrease,which was accompanied by cell morphology changes.The combined toxicity was then confirmed as ROS associated oxidative stress with up to 300% and 35% increase of the intracellular ROS level and glutathione S-transferase (GST) activity,respectively.N-acetylcysteine (NAC) can also provide almost complete protection against the induced toxicity.Therefore,the ROS associated oxidant injury might be responsible for the QDs-Cu2+/Cu2+ induced toxicity and could be balanced through cytoprotective antioxidant enzyme GST.     

紫外光降解反应器去除氯苯气体模型的建立与应用

从光化学反应过程出发,基于线性光源球面辐射能量分布（LSSE）,以反应器内部空间的辐射能吸收密度、空塔停留时间、进口浓度等为主要参数,建立了气相环境中紫外光化学反应器去除氯苯的数学模型.结果表明,建立的模型能很好地模拟和预测紫外光化学反应器对氯苯气体的去除性能.氯苯气体的紫外光化学反应表现出一级反应动力学的特征.该模型包含了紫外光降解反应器设计的主要参数,同时被用于预测了反应器在不同进口浓度和不同空塔停留时间条件下的出口氯苯浓度,进而获得不同进口浓度达标排放所需要的最小空塔停留时间,为气相污染物的紫外光降解反应器的设计与运行提供了重要的理论指导.     

春季太湖光量子产额空间分布的特征分析

基于2009年4月28日、5月4日、5月5日及5月6日在太湖梅梁湾的栈桥头、直湖港的河口区、太湖中心及胥口湾中心测定的初级生产力及水下光场数据,计算了各测点的藻类光量子产额和P-I曲线,并分析了其空间差异的特征.太湖栈桥头的P-I曲线呈现出明显的光抑制现象;在胥口湾中心和直湖港河口,P-I曲线呈现出弱的光抑制现象;而在太湖中心区域,P-I曲线只达到了光饱和状态,并未出现光抑制现象.单位叶绿素a的最大光量子产额的大小顺序为太湖中心区域、梅梁湾的栈桥头、直湖港的河口区及胥口湾的湖心区.     

An environmental impact assessment of quantum dot photovoltaics (QDPV) from raw material acquisition through use

Some emerging technologies are expected to be pivotal for solving many of the environmental challenges faced today, especially those related to energy. However, many of these technologies may incur significant environmental impacts over their life cycle, while having environmental benefits during their use. This paper presents results of a Life Cycle Assessment (LCA) of a proposed type of nanophotovoltaic, quantum dot photovoltaic (QDPV) module. The LCA is confined to the stages of raw materials acquisition, manufacturing, and use. The impacts of QDPV are compared with other types of PV modules and energy sources - both renewable and nonrenewable. To provide a comprehensive comparative assessment, QDPV modules were compared with mature as well as emerging PV types for which data are available. Comparative assessment with other types of energy sources includes coal, oil, lignite, natural gas, diesel, nuclear, wind, and hydropower.QDPV modules may have the potential to overcome two current barriers of solar technology: low efficiencies and high manufacturing costs. If higher efficiencies are realized, QDPV modules could pave the way to large scale implementation of solar energy, helping nations move toward greater energy independence. On the other hand, candidate materials as quantum dots for solar cell applications are mostly compound semiconductors such as cadmium selenide, cadmium telluride, and lead sulfide which may be toxic and for which renewable options are limited. Toxic effects of these materials may be exacerbated by their nanoscale features.The LCA was carried out using the software SimaPro, and the Ecoinvent Life Cycle Inventory (LCI) database supplemented with available literature and patent information. Our results indicate that while QDPV modules have shorter Energy PayBack Time (EPBT), lower Global Warming Potential (GWP), SO_x and NO_x emissions than other types of PV modules, they have higher heavy metal emissions, underscoring the need for investigation of emerging technologies, especially nano-based ones, from a life cycle perspective. QDPV modules are better in all impact categories assessed than carbon-based energy sources but they have longer EPBT than wind and hydropower and higher GWP.     

纳米二氧化钛复合石墨烯催化剂的制备及处理染料废水

以硫酸钛为原料,采用共沉淀法,制备了一系列纳米二氧化钛复合石墨烯催化剂,采用XRD和FTIR对样品进行表征。通过紫外光照射亚甲基蓝溶液光催化降解实验,研究石墨烯的加入量对TiO2光催化性能的影响,结果表明,TiO2-GO-5具有最佳的光催化性能。在pH=6.00、TiO2-GO-5的投加量为0.070 g/50 mL、光照3 h条件下,100 mg/L亚甲基蓝溶液的脱色率达到最大值为90.52%。     

纳米TiO2-石墨烯光催化剂的水热合成及其光催化性能

以钛酸四正丁酯和石墨为原料，通过水热法制备了锐钛矿型为主的纳米TiO2复合光催化剂（纳米TiO2-石墨烯），并采用XRD，FTIR，FESEM，TEM技术对其进行了表征。通过紫外光照射降解溶液中的罗丹明B（RhB）研究了TiO2-石墨烯的光催化活性，分析了初始罗丹明B质量浓度、催化剂加入量、溶液pH和催化剂使用次数等影响降解效果的因素。实验结果表明：在初始RhB质量浓度为20 mg/L、溶液pH为7.10、催化剂加入量为1.000 g/L的条件下，紫外光照射30 min时，纳米TiO2-石墨烯对RhB的降解率高达98.69%，明显高于纳米TiO2的44.69%;纳米TiO2-石墨烯稳定性较强，可多次重复使用。     

石墨烯纳米材料对哺乳动物的毒性及其作用机制

石墨烯是一种应用广泛的新兴非金属纳米材料，具有独特的电学机械性能、超大的比表面积以及潜在的生物相容性，在材料、电子、能源、光学以及生物医学等领域得到广泛应用。与此同时，石墨烯的环境行为和生物毒性也随之引起日益广泛的关注。本文通过对石墨烯纳米材料的动物毒性、细胞毒性、毒性影响因素和毒性机制等相关研究进展进行总结。石墨烯纳米材料可通过气管滴注、吸入、静脉注射、腹腔注射以及口服等方式进入体内，通过机械屏障、血脑屏障和血液胎盘屏障等积累在肺、肝、脾等部位引起急性或者慢性损伤；目前有关石墨烯毒性机制的研究主要集中于线粒体损伤、DNA损伤、炎性反应、凋亡等终点及氧化应激参与的复杂信号通路，不同石墨烯纳米材料的浓度、尺寸、表面结构和官能团等对石墨烯的生物毒性影响不同。鉴于当前该领域研究的局限性，对石墨烯纳米材料生物毒性研究的发展方向进行了展望，进而为石墨烯材料的安全应用提供理论借鉴和实践参考。