有机磺酸类化合物的络合萃取研究

本文以三烷基胺为络合剂,正辛醇,煤油,氯仿,四氯化碳等为稀释剂,测定了络合萃取剂对于对甲基苯磺酸,磺基水杨酸稀溶液的相平衡分配系数,讨论了稀释剂,体系ＰＨ值和７３０１络合剂含量对萃取相平衡分配系数Ｄ值的影响,确定了形成的萃合物的组成。     

浙江省海岸带优势资源及其组合特点

浙江省海岸带以自然资源集聚、种类众多为其特色，它为振兴浙江经济提供了极为有利的条件。浙江海岸带有六项优势资源，即港口航道资源、水产资源、滩涂土地资源、海洋能资源、旅游资源以及岛屿资源。本文分析了这些优势资源的组合特点，并指出优势资源存在着多宜性、动态性，在开发利用过程中要加以综合规划，统一协调，目的是以期引起有关方面注意，采纳或参考。     

湿法烟气脱硫废水处理技术探讨

分析了火电厂湿法烟气脱硫装置排水的主要成分、水质特点，叙述了烟气湿法脱硫废水国内外的处理方法和工艺流程。结合笔者实践，提出了一种改进的处理方法，为湿法脱硫废水处理提供了一种有效的途径。     

Development of a continuously stirred flow cell for investigating sorption mass transfer

This paper introduces a new reversible-flow design for a continuously stirred reactor used to study sorption mass transfer in soil and solvent systems. The stirred reactor has potential advantages over conventional packed column or batch reactors because it isolates intraparticle sorption rate limitations from advective-dispersive transport, yet allows changes to flux through the reactor for analysis of sorption kinetics under dynamic conditions. Previously, stirred reactors have often failed due to clogging of sediment on the effluent frit. The reverse-flow backwashing design allows longer life and higher confidence in maintaining mixed conditions than previous designs. Mass transfer 'rate coefficients estimated from stirred and column experiments are compared; both techniques produced results consistent with a published correlation. The data also show that fitted sorption mass transfer coefficients can be strongly dependent on the choice of equilibrium partition coefficient (i.e. batch or first-moment derived values), and that the conventional two-site sorption kinetics model fails to accurately predict sorption mass transfer in the presence of changing solvent velocity through the reactor.     

Plant uptake of aldicarb from contaminated soil and its enhanced degradation in the rhizosphere

Experiments were conducted to investigate the degradation of aldicarb, an oxime carbamate insecticide, in sterile, non-sterile and plant-grown soils, and the capability of different plant species to accumulate the pesticide. The degradation of aldicarb in soil followed first-order kinetics. Half lives (t1/2) of aldicarb in sterile and non-sterile soil were 12.0 and 2.7 days, respectively, which indicated that microorganisms played an important part in the degradation of aldicarb in soil. Aldicarb disappeared more quickly (p< or =0.05) in the soil with the presence of plants, and t1/2 of the pesticide were 1.6, 1.4 and 1.7 days in the soil grown with corn, mung bean and cowpea, respectively. Comparison of plant-promoted degradation and plant uptake showed that the enhanced removal of aldicarb in plant-grown soil was mainly due to plant-promoted degradation in the rhizosphere.     

Characteristics of single atmospheric particles in a heavily polluted urban area of China: size distributions and mixing states

To investigate the chemical composition, size distribution, and mixing state of aerosol particles on heavy pollution days, single-particle aerosol mass spectrometry was conducted during 9–26 October 2015 in Xi’an, China. The measured particles were classified into six major categories: biomass burning (BB) particles, K-secondary particles, elemental carbon (EC)–related particles, metal-containing particles, dust, and organic carbon (OC) particles. BB and EC-related particles were the dominant types during the study period and mainly originated from biomass burning, vehicle emissions, and coal combustion. According to the ambient air quality index, two typical episodes were defined: clean days (CDs) and polluted days (PDs). Accumulation of BB particles and EC-related particles was the main reason for the pollution in Xi’an. Most types of particle size were larger on PDs than CDs. Each particle type was mixed with secondary species to different degrees on CDs and PDs, indicating that atmospheric aging occurred. The mixing state results demonstrated that the primary tracers were oxidized or vanished and that the amount of secondary species was increased on PDs. This study provides valuable information and a dataset to help control air pollution in the urban areas of Xi’an.

Graphical abstract

     

不锈钢波纹管在海洋大气环境下的腐蚀失效分析

目的 研究热带海洋大气环境下06Cr19Ni10不锈钢波纹管的腐蚀失效机理。方法 对失效导管进行宏观形貌分析,确定宏观腐蚀特征。进一步对失效管段进行显微组织以及化学成分的分析。采用体式显微镜、扫描电镜(SEM)和能谱分析(EDS)开展失效管段的微观腐蚀形貌观察和腐蚀产物分析。结果 宏观来看,导管上金属网套和波纹管外面有几处轻微腐蚀,波纹管侧面腐蚀略微严重,内部没有发现腐蚀。金相组织显示,波纹管基体材料为奥氏体晶粒,在U型波纹管顶部有少量马氏体存在,波纹管基体材料化学成分符合国标要求。扫描电镜下,波纹管外表面发生了严重的点蚀,在U型波纹管的顶部和波纹间的平台均有较大的点蚀坑,U型顶部的点蚀更为严重,并且波纹管不同部位发生了明显的晶间腐蚀。点蚀坑处的EDS显示,腐蚀产物多为Fe的氧化物,坑内还发现了少量的Cl^?,并且坑内产物的Cr元素含量明显少于基体。结论 由于波纹管固溶处理不当,导致晶界间贫铬,使材料表面大部分区域产生晶间腐蚀。同时由于波纹管顶部的塑性变形诱导马氏体生成,使得该处更容易发生点蚀,而海洋大气环境中的氯离子进一步促进了这种点蚀的发生,最终导致了波纹管的腐蚀失效,U型顶端发生的点蚀是材料失效的主要原因。     

Concurrent catalytic removal of typical volatile organic compound mixtures over Au-Pd/α-MnO2 nanotubes

α-MnO_2 nanotubes and their supported Au-Pd alloy nanocatalysts were prepared using hydrothermal and polyvinyl alcohol-protected reduction methods, respectively. Their catalytic activity for the oxidation of toluene/m-xylene, acetone/ethyl acetate, acetone/m-xylene and ethyl acetate/m-xylene mixtures was evaluated. It was found that the interaction between Au-Pd alloy nanoparticles and α-MnO_2 nanotubes significantly improved the reactivity of lattice oxygen, and the 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst outperformed the α-MnO_2 nanotube catalyst in the oxidation of toluene, m-xylene, ethyl acetate and acetone. Over the0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst,(i) toluene oxidation was greatly inhibited in the toluene/m-xylene mixture, while m-xylene oxidation was not influenced;(ii) acetone and ethyl acetate oxidation suffered a minor impact in the acetone/ethyl acetate mixture; and(iii) m-xylene oxidation was enhanced whereas the oxidation of the oxygenated VOCs(volatile organic compounds) was suppressed in the acetone/m-xylene or ethyl acetate/m-xylene mixtures. The competitive adsorption of these typical VOCs on the catalyst surface induced an inhibitive effect on their oxidation, and increasing the temperature favored the oxidation of the VOCs. The mixed VOCs could be completely oxidized into CO_2 and H_2 O below 320°C at a space velocity of 40,000 m L/(g·hr). The 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst exhibited high catalytic stability as well as good tolerance to water vapor and CO_2 in the oxidation of the VOC mixtures. Thus, the α-MnO_2 nanotube-supported noble metal alloy catalysts hold promise for the efficient elimination of VOC mixtures.     

Preparation of ceria-zirconia solid solution with enhanced oxygen storage capacity and redox performance

A new method called ultrasonic-assisted membrane reaction (UAMR) was reported for the fabrication of ceria-zirconia solid solution. A series of ceria-zirconia solid solutions with different Ce/Zr molar ratios were prepared by the UAMR method and characterized by X-ray diffraction (XRD), N₂ adsorption, hydrogen temperature-programmed reduction (H₂-TPR), scanning electron microscope (SEM), and transmission electron microscopy (TEM) techniques. The UAMR method proved to be superior, especially when the Ce/Zr molar ratio was lower than 1, in fabricating ceria-zirconia solid solutions with large BET surface area, high oxygen storage capacity (OSC), and low reduction temperature.