A pyrazine based metal-organic framework for selective removal of copper from strongly acidic solutions

● pz-UiO-66 was synthesized facilely by a solvothermal method. ● Efficient capture of copper from highly acidic solution was achieved by pz-UiO-66. ● pz-UiO-66 exhibited excellent selectivity and capacity for copper capture. ● Pyrazine-N in pz-UiO-66 was shown to be the dominant adsorption site. The selective capture of copper from strongly acidic solutions is of vital importance from the perspective of sustainable development and environmental protection. Metal organic frameworks (MOFs) have attracted the interest of many scholars for adsorption due to their fascinating physicochemical characteristics, including adjustable structure, strong stability and porosity. Herein, pz-UiO-66 containing a pyrazine structure is successfully synthesized for the efficient separation of copper from strongly acidic conditions. Selective copper removal at low pH values is accomplished by using this material that is not available in previously reported metal–organic frameworks. Furthermore, the material exhibits excellent adsorption capacity, with a theoretical maximum copper uptake of 247 mg/g. As proven by XPS and FT-IR analysis, the coordination of pyrazine nitrogen atoms with copper ions is the dominant adsorption mechanism of copper by pz-UiO-66. This work provides an opportunity for efficient and selective copper removal under strongly acidic conditions, and promises extensive application prospects for the removal of copper in the treatment for acid metallurgical wastewater.     

飞机起落架材料防护技术现状及研究进展

介绍了飞机起落架高强度钢的防护工艺及其防护特点。传统的防护工艺主要是镀铬和镀镉工艺,目前出现了无氰镀镉-钛、高速火焰喷涂(HVOF)涂层、低氢脆刷镀镉等新型防护工艺。通过对各新型防护工艺与传统工艺的工艺性能及耐腐蚀性能进行对比发现,各新型防护工艺都能很好地取代传统的防护工艺应用于飞机起落架的保护。     

昌江核电站运营前附近海域总β放射性水平

在昌江核电站运营前,研究人员对其附近海域做了水质、沉积物和海洋生物总β放射性调查,并与我国其他海域及昌江核电站周围的陆地环境做了对比。结果表明:（1）海水样品总β比活度范围为0.040～0.074 Bq/L,平均值为0.054 Bq/L,与渤海、黄海、东海、南海近海、大亚湾核电站等海域相比,昌江核电站海域海水中总β放射性水平相对较低;（2）表层沉积物中总β比活度范围为257～925 Bq/kg,平均值为653 Bq/kg,研究海域沉积物中总β放射性水平与香港、青岛、阳江等海域水平相当;（3）海洋生物样品中总β比活度范围为8.7～63.8 Bq/kg,平均值为48.0 Bq/kg,海鱼类、虾类和贝类体内总β平均值分别为56.7 Bq/kg、63.4 Bq/kg和24.0 Bq/kg,鱼类和虾类明显大于贝类。本研究可为今后科学、合理地评价核电站运行对海洋环境的影响提供重要的数据支撑。     

Effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria: Soot-ceria contact and interfacial oxygen evolution

Ceria is widely used as a catalyst for soot combustion, but effects of Zr substitution on the reaction mechanism is ambiguous. The present work elucidates effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria. The nanostructured CeO₂, Ce_0.92Zr_0.08O₂, and Ce_0.84Zr_0.16O₂ composed of 5–6 nm crystallites display T_m-CO2 (the temperature at maximum CO₂ yield) at 383, 355, and 375°C under 10 vol.% O₂/N₂, respectively. The size of agglomerate decreases from 165.5 to 51.9–57.3 nm, which is beneficial for the soot-ceria contact. Moreover, Zr increases the amount of surface oxygen vacancies, generating more active oxygen (O₂^? and O^?) for soot oxidation. Thus, the activities of Ce_0.92Zr_0.08O₂ and Ce_0.84Zr_0.16O₂ in soot combustion are better than that of CeO₂. Although oxygen vacancies promote the migration of lattice O^2?, the enriched surface Zr also inhibits the mobility of lattice O^2?. Therefore, the T_m-CO2 of Ce_0.84Zr_0.16O₂ is higher than that of Ce_0.92Zr_0.08O₂. Based on reaction kinetic study, soot in direct contact with ceria preferentially decomposes with low activation energy, while the oxidation of isolated soot occurs through diffusion with high activation energy. The obtained findings provide new understanding on the soot combustion over nanoceria.     

改性Ti/SnO2-Sb电极催化降解1,4-二氯苯废水试验研究

采用聚合物前驱体法制备了未掺杂、掺杂Cu、掺杂Bi、掺杂Ni的4种Ti/Sn O2-Sb电极,运用SEM和XRD分析电极表面形貌及结构,通过线性极化扫描、循环伏安等测试考察其电化学性能,同时进行1,4二氯苯(p-DCB)降解实验进一步探究电极的电催化氧化特性.SEM和XRD结果表明,掺杂金属可改善电极表面形貌,增大其比表面积;电化学测试表明,Ti/Sn O2-Sb电极的析氧电位并未因金属掺杂而有明显改变,掺杂金属后,Ti/Sn O2-Sb电极具有更优的电催化活性和稳定性.p-DCB降解实验表明,改性Ti/Sn O2-Sb电极对p-DCB的降解效率明显提高,其中Ti/Sn O2-Sb-Cu电极的电催化处理效果最优,电解2 h后p-DCB的去除率即达到87.6%,且p-DCB的降解反应遵循一级反应动力学规律.     

气象灾害静动态风险管理析探

带着气象灾害风险管理存在分类不清的问题,应用相关资料和云南气象灾害风险管理的实例,初步将气象灾害风险管理分为静、动态两类,并进行定义、过程、目标、任务方面的对比分析。结果表明:气象灾害风险管理不论从风险定义、管理过程、研究与应用的技术方法、结果、目标上都存在明显的差异,划分为静态和动态风险管理是应该的,具有理论和应用价值;静态风险管理和动态风险管理都是气象灾害防御体系中的重要组成部分,能从不同的角度提高防灾减灾的能力和水平,静态风险管理主要基于气候研究技术,动态风险管理主要基于天气研究技术;气象灾害静态风险管理已有了一些研究和应用成果,而动态风险管理还处在探索阶段。     

浙江省沿海地区农村房屋抗风情况调研

对浙江省沿海地区的农村房屋抗风情况进行了调研,总结了被破坏房屋的主要结构特点。在对现有房屋的统计中发现相对不富裕地区高达60%以上的房屋属于抗风能力差和较差的,而一些比较富裕且受过台风袭击有过惨痛教训地区的房屋抗风能力差和较差的仅在20%以下。进一步研究发现抗风能力较好的房屋大都是建造年代不久,多为混凝土现浇板屋盖,上部多为框架或砖混结构,而抗风能力较差和差的大都为建造年代已久,多为小青瓦屋面,上部结构多为砖木结构或构造措施较差的砖混结构。同时对当地村民传统的"砖头压瓦"防护措施进行理论验算,得出当风速超过台风界限风速时,屋面上的砖头将会飞起,该措施应该避免。     

震后灾害链生机制及其对汶川地震城镇重建的影响

汶川8级大地震对地表产生强烈扰动,导致次生山地灾害极度发育,影响到震后灾害的活动特征及其相应的减灾对策。震后松散固体物质急剧增加、流域微地貌变化明显(沟道堵塞严重)、水文变化利于侵蚀和洪峰,使得灾害群发链生:崩塌、滑坡→泥石流→堰塞湖→溃决洪水(泥石流),8月中旬灾区各地因强降雨而大规模爆发泥石流堵塞河道,洪水冲毁掩埋重建城镇,给地震重灾区造成巨大损失。从以汶川县映秀镇为例,在阐述灾害链研究成果的基础上,分析震后灾害链的形成条件、成灾过程以及对城镇重建居民点的危害特点,进而提出灾害防治措施,为灾后城镇建设防灾减灾提供参考建议。     

基于合成孔径雷达的城市建筑地震受损分析

汶川地震灾区位于青藏高原东缘,该地区云雨天气较多,光学遥感受制约较大,而微波能够穿透云、雾、小雨等,且不受太阳光线的影响,雷达遥感具有全天时、全天候的特点,因而可以弥补光学遥感的不足。根据房屋受地震破坏后影响雷达回波强度,在雷达影像上表现为亮度及纹理不同的原理,本论文利用不同分辨率的COSMO-SkyMed和Radarsat等SAR数据,将其与震前的SPOT影像进行配准后,通过纹理分析等处理,对都江堰市区、北川县城曲山镇等受灾较为严重的城镇进行分析解译,利用雷达影像判读出倒塌房屋的信息,以及地震次生山地灾害对城镇的破坏。     

Kinetics of aniline oxidation with chlorine dioxide

For the first time, kinetics of aniline oxidation with chlorine dioxide(ClO2) were investigated systematically by detecting concentration of aniline with HPLC at regular intervals. Results showed that the reaction was first-order both in ClO2 and in aniline, and the oxidation reaction could be described as second-order reaction. Stoichiometric factor η was experimentally determined to be 2.44. The second-order-reaction rate constant k was 0.11L/(mol.s)under condition of pH 6.86 and water temperature(Tw) 287K. Reaction activation energy was 72.31 kJ/mol, indicating that the reaction could take place under usual water treatment conditions. The reaction rate constants in acidic and alkali media were greater than that in neutral medium. Chlorite ion could slightly increase reaction rate in acidic medium. p-aminophenol and azobenzene were detected by GC-MS as intermediates.