长三角地区跨区域合作创新对区域多样化的影响研究

区域多样化发展在提高生产力、促进就业以及稳定经济等方面发挥着重要作用.一直以来演化经济地理学框架下区域多样化发展中外部资源的作用被忽略,而跨区域合作创新是区域获取外部知识的重要途径之一.研究使用2000～2017年长三角地区41个城市的发明专利数据,对区域经济一体化特征显著的长三角地区多样化水平与合作创新进行测度,并实证检验区域内部与跨区域的合作创新在区域多样化进程中所发挥的作用.结果表明:(1)长三角地区各城市的相关与不相关多样化水平总体呈现逐渐上升并趋于稳定的趋势;(2)合作创新作为知识流动的重要载体,合作参与者大多位于长三角内,合作创新所产生的知识溢出往往发生在具有技术关联性的产业间,从而有助于促进长三角地区发展相关多样化,但对不相关多样化没有表现出显著影响;(3)合作创新中参与团队数量与区域相关与不相关多样性没有显著关系;(4)合作创新中跨区域合作比例越高,越能够促进区域相关与不相关多样化的发展.因此,在推动区域产业多样化的过程中应注重强化区域间的合作,借助外部力量引导区域产业发展.     

覆冰输电塔-线体系风致动力响应分析

依据流体诱发振动原理,结合已有覆冰计算模型,考虑降雨的分类,模拟了输电塔-线体系不同高度导线的覆冰和风荷载。以东北地区某输电塔为例,对覆冰输电塔-线体系在稳定风速激励下的动力响应进行分析,并与不考虑塔线耦联的导线舞动分析结果及覆冰塔线拟静力的分析结果进行对比,对塔位移、输电线位移、钢材应力进行了分析。研究结果表明:塔-线耦联体系对覆冰导线风振有很大影响,覆冰输电塔抗风设计安全度需要进一步提高。     

Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized water treatment

• Gas diffusion electrode (GDE) is a suitable setup for practical water treatment. • Electrochemical H₂O₂ production is an economically competitive technology. • High current efficiency of H₂O₂ production was obtained with GDE at 5–400 mA/cm². • GDE maintained high stability for H₂O₂ production for ~1000 h. • Electro-generation of H₂O₂ enhances ibuprofen removal in an E-peroxone process. This study evaluated the feasibility of electrochemical hydrogen peroxide (H₂O₂) production with gas diffusion electrode (GDE) for decentralized water treatment. Carbon black-polytetrafluoroethylene GDEs were prepared and tested in a continuous flow electrochemical cell for H₂O₂ production from oxygen reduction. Results showed that because of the effective oxygen transfer in GDEs, the electrode maintained high apparent current efficiencies (ACEs,>80%) for H₂O₂ production over a wide current density range of 5–400 mA/cm², and H₂O₂ production rates as high as ~202 mg/h/cm² could be obtained. Long-term stability test showed that the GDE maintained high ACEs (>85%) and low energy consumption (<10 kWh/kg H₂O₂) for H₂O₂ production for 42 d (~1000 h). However, the ACEs then decreased to ~70% in the following 4 days because water flooding of GDE pores considerably impeded oxygen transport at the late stage of the trial. Based on an electrode lifetime of 46 days, the overall cost for H₂O₂ production was estimated to be ~0.88 $/kg H₂O₂, including an electricity cost of 0.61 $/kg and an electrode capital cost of 0.27 $/kg. With a 9 cm² GDE and 40 mA/cm² current density, ~2–4 mg/L of H₂O₂ could be produced on site for the electro-peroxone treatment of a 1.2 m³/d groundwater flow, which considerably enhanced ibuprofen abatement compared with ozonation alone (~43%–59% vs. 7%). These findings suggest that electrochemical H₂O₂ production with GDEs holds great promise for the development of compact treatment technologies for decentralized water treatment at a household and community level.     

废彩色阴极射线管玻璃的X和γ射线屏蔽特性

废电视机和计算机监视器产生了数量庞大的废阴极射线管（CRTs）,已成为全球面临的环境风险,迫切需要找出新的处置方法和再利用途径来化解风险。用Χ和γ射线标准剂量测定装置(QH16),XRF,ICP,XRD和灰熔点炉等试验手段测试了废彩色CRTs玻璃的铅当量、化学组成和烧结等特性,并与钢、铁矿石、重晶石等进行对比;讨论了废彩色CRTs玻璃的X和γ射线质量衰减系数,能量吸收特性和辐射屏蔽能力。结果表明,废彩色CRTs玻璃所含的Pb、Ba、Sr、Sb、Ce、Zn等金属元素具有优良的Χ和γ射线屏蔽性能,将其通过烧结法制备成射线屏蔽材料是控制污染和再利用的有效途径。     

废镍镉电池处置和金属回收关键技术研究进展

系统地介绍了处置废镍镉电池所涉及预处理、蒸馏、浸出、湿法分离和三废处理的关键技术,尤其是真空冶金、生物冶金、乳状液膜分离的研究成果,并对比了不同工艺对环境的影响。     

SiO_3~(2-)离子的加入对脉冲倒极电解合成PASiC的研究

探索了试验过程中SiO2 -3 离子团的加入对脉冲自动倒极电解法合成聚合氯化硅酸铝中Alb 含量的影响。通过试验确定了最佳摩尔比。在脉冲倒极周期和电解槽电流一定的情况下 ,当总铝AlT 与SiO2 -3 的摩尔比为 10∶1～ 2 0∶1时 ;在此合成条件下制备液中Alb 含量超过 80 % ;处理模拟水样最佳投药量为 :0 5～ 5mgAl2 O3 /L。在制备过程中 ,极化现象得到了极好的控制 ,电解槽电压和电流十分稳定     

Occurrence of PAHs, PCBs and organochlorine pesticides in the Tonghui River of Beijing, China

Tonghui River, a typical river in Beijing, People's Republic of China, was studied for its water and sediment quality, by determining the levels of 16 polycyclic aromatic hydrocarbons (PAHs), 12 polychlorinated biphenyls (PCBs) and 18 organochlorine pesticides in water and sediment samples. Total PAHs, PCBs and organochlorine pesticides concentrations in water varied from 192.5 to 2651 ng/l, 31.58-344.9 ng/l and 134.9-3788 ng/l, respectively. The total PAHs, PCBs and organochlorine pesticides concentrations in surficial sediments were 127-928 ng/g, 0.78-8.47 ng/g and 1.79-13.98 ng/g dry weight, respectively. The results showed that the concentration of these selected organic pollutants in sediment was higher than those in surface water. It may be due to the fact that organic hydrophobic pollutants tend to stay in the sediments. The PAHs were dominated by 2-, 3-ring components in water samples and by 3- and 4-ring compounds in sediment. For organochlorines, alpha-HCH, delta-HCH, Heptachlor, Endosulfan II, DDT are the major organochlorine pesticides in water while Heptachlor, Dieldrin and DDE composed of 95% of total organochlorine pesticides in sediment. For HCHs (HCHs=alpha-HCH+beta-HCH+gamma-HCH+delta-HCH), the predominance of alpha-HCH of total HCHs were clearly observed in water and sediment. PCB18, PCB31 and PCB52 were predominant in water, on average these compounds collectively accounted for 67% of total PCBs. But in sediment, the predominant compounds were PCB28, PCB31 and PCB153, which accounted for 71% of total PCBs in sediment. The levels of micro pollutants in our study areas were compared with other studies.     

电解氧化法处理黄金冶炼厂选冶废水

采用电解氧化法处理同时含有高浓度氰化物与COD的黄金冶炼厂选冶废水,主要考查了外加电压、溶液pH、电解时间及极板间距等因素对氰化物和COD去除率的影响,充分利用原水中Cl^-的阳极氧化效应,深入探讨了电化学氧化过程及污染物氧化去除机理。结果表明,随着外加电压和电解时间的增大,氰化物和COD去除率逐渐增大。以石墨为阳极,钛合金为阴极,采用一阴两阳电解体系对废水进行氧化,当电压为4.5 V、初始pH为7、电解时间为3 h、极板间距为1.5 cm的条件下,总氰化物 (CN_T) 、COD、SCN^-及Cu的去除率最高可达99.6%、96%、99.9%与99.2%。电解过程中体系pH逐渐降低,电场作用下定向迁移至阳极附近的污染物去除主要归因于HClO及ClO^-的间接氧化作用,当pH大于5.0时以HClO的氧化为主,ClO^-的氧化为辅,而pH小于5.0时则主要是HClO的氧化。电解氧化过程中约有36.17%的Cu与SCN^-形成CuSCN沉淀而被除去,剩余的铜则扩散至阴极沉积析出。GC-MS分析表明,烷烃类、酯类、酮类等大分子的C=C键、酯基、羰基等化学键和官能团被氧化断链成小分子物质,随后继续被氧化为H₂O、CO₂和N₂。     

Photocatalytic oxidation of triclosan

In the spring of 2003, there was an outbreak of the severe respiratory syndrome (SARS) in Hong Kong. Health concerns have thus triggered an increased and predominant use of various types of household cleansing agents such as triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol). However, it has been reported recently that triclosan could be photochemically converted to toxic 2,8-dichlorodibenzo-p-dioxin (2,8-Cl(2)DD) in the environment. It is therefore necessary to develop environmentally friendly methods for the treatment of triclosan. To this end, photocatalytic degradation of triclosan in aqueous solution was conducted using TiO(2) (Degussa P25) under irradiation of UV light (lambda < 365 nm). It was found that triclosan could be degraded by this approach. Hydrogen peroxide was added to enhance the degradation process, and the optimal initial hydrogen peroxide concentration for triclosan degradation was 0.005% (w/v). Product identification indicated that triclosan oxidation occurred at its phenol moiety and yielded quinone and hydroquinone intermediates. The formation of a dichlorophenol intermediate in triclosan degradation suggested bond-breaking of the ether linkage occurred during the process. Moreover, no chlorinated dibenzo-p-dioxin congener was detected. These findings confirm that the photocatalytic degradation of triclosan is an environmentally friendly process.     

西安市2013年PM_(2.5)浓度变化分析研究

全面分析2013年西安市13个国控环境空气质量自动监测子站PM2.5监测数据。结果表明:2013年西安市环境空气中PM2.5年均值为105μg/m3,超过《环境空气质量标准》(GB 3095—2012)二级要求(35μg/m3)200.0%,污染较严重;西安市各子站PM2.5月均值总体呈两边高、中间低的"V"型趋势,全市及各子站PM2.5月均值分别为44~206、32~275μg/m3;采暖期(上半年采暖期为1—3月,下半年采暖期为11—12月)、非采暖期(4—10月)PM2.5平均值分别为156、70μg/m3;上、下半年采暖期PM2.5平均值分别为178、124μg/m3;西安市气象风力以微风为主,雨天集中在5—9月,期间PM2.5月均值小于80μg/m3。