从产品检测看安防技术的发展和行业走向

1产品检测是质量监督的重要手段 世界各国、特别是发达国家都是通过产品检测手段来促进公平的市场竞争、保障消费者权益、建立技术壁垒.但具体作法与我国有很大的差别.在市场经济体制完善的国家,社会监督机制起主导作用,厂家的自我约束意识和消费者的自我保护意识很强.所以产品检测主要是厂家自愿的行为.     

基于模型推断法确定邛海总磷总氮浓度的参照状态

将流域入湖的氮磷负荷分为点源和非点源两部分,基于SCS模型和USLE模型,分别计算了流域入湖的溶解态和颗粒态非点源负荷,根据沿湖城镇、湖滨居民点生活污水及养殖废水排放,计算了入湖的点源负荷。通过出湖河流、湖内取水和渔产捕捞,计算了出湖的营养物负荷。通过计算的出、入湖负荷和现有的湖泊水体氮磷浓度数据,基于湖泊氮磷质量守恒,计算了氮磷的净沉降速度。根据计算的逐年入湖氮磷负荷和所建的湖泊氮磷质量守恒模型,逆推逐年的湖泊水体氮磷浓度,确定湖泊氮磷浓度的参照状态。应用建立的模型推断出邛海TP、TN浓度的参照状态分别为0.018和0.239 mg/L。构建的湖泊氮磷参照状态推断模型,所需资料少,概念清晰,在资料缺乏的其他湖泊流域具有推广应用价值。     

铁屑耦合固相反硝化对低碳氮比废水中总氮的处理

为考察脱氮效率并解决碳源不足导致总氮 (TN) 去除率不高的问题,将竹刨花作为固体碳源与挂膜载体,引入铁屑,构成耦合体系,搭建2套反硝化实验装置 (分别为耦合体系1号与单纯固相反硝化体系2号) 并对脱氮率及微生物进行分析。结果表明：进水TN为41.62~59.95 mg·L⁻¹,COD/N<0.5,水力停留时间为18 h; 13~105 d,1号TN平均去除率为73.21%~92.79%,比2号平均去除率高近1倍;1号碳源相对2号更为充足,但2体系出水COD均值都低于一级A;1号总铁释放稳定,出水总铁均值低于0.3 mg·L⁻¹,未出现NH₃-N明显积累。SEM表征结果显示,1号竹填料表面黏性物质与微生物数量更多,生物膜更加紧密。16S rRNA表征结果显示：1号具有更高的微生物丰度与多样性;2体系反硝化脱氮相关门类占主体,优势门类均为变形菌门,但1号变形菌门占比高于2号;变形菌门中,1号反硝化菌群 (属水平,丰度>1%) 类别和总占比均高于2号。由此可知,铁屑强化了碳源的分解与利用,促进了脱氮功能菌生长,显著提升了耦合体系脱氮效能,出水TN可达到地表水IV类标准(GB 3838-2002)。竹刨花获取方便灵活,铁屑低廉,两者构成的耦合体系具有巨大的实际应用前景。     

岸线码头密度对河道水动力和污染物输移影响分析——以武汉河段为例

为研究岸线码头密度对河流水动力变化及污染物输移的影响,以武汉河段为例,基于Mike21模型建立了适用于该河段的平面二维水动力-水质模型,计算了长为9.6 km的岸线范围内布置不同密度码头群后引起的附近区域内水位、流速变化以及突发水污染事故后的自净能力变化,从空间差异性、最大变幅等角度对比了三者的差异,并归纳了码头密度与水动力条件、污染物浓度变幅之间的关系.结果 表明:(1)随着码头密度增加,工程区上游水位变化较流速更敏感,工程区及下游局部位置水位变幅较小,而流速变化较为敏感,表现为前沿主流区流速增大,近岸区流速减小;当码头密度大于1.25～2.5座/km的临界范围后,水动力条件随码头密度的变幅逐渐减缓.(2)修建码头后,受水动力变化影响,工程区河段上游污染物浓度变化呈"峰前减、峰后增",但工程区下游呈"峰前增、峰后减"的特征;工程区间内表现为主流区浓度增大、近岸带浓度减小、高浓度滞留时间总体增加的变化特点.(3)受码头工程群影响,无论是区间整体上,还是局部范围内,污染物浓度相对水动力条件变幅更大,对河段内水源地的取水可能造成不利影响.以上认识对于河流岸线开发利用规模选取和效应评估具有参考意义.     

Probabilistic health risk assessment of nitrosamines in drinking water of Shaoxing,Zhejiang, China

Environmental Science and Pollution Research - Nitrosamines (NAms) are potent genotoxic and carcinogenic but widely detected in drinking water. This study aimed to investigate the occurrence of...     

Enhanced arsenate removal from aqueous solution by Mn-doped MgAl-layered double hydroxides

Environmental Science and Pollution Research - In this study, Mn-doped MgAl-layered double hydroxides (LDHs) were successfully synthesized for efficient removal arsenate from aqueous solution. The...     

Study on the denitrification performance of FexLayOz/activated coke for NH3-SCR and the effect of CO escaped from activated coke at mid-high temperature on catalytic activity

Currently, activated coke is widely used in the removal of multiple pollutants from industrial flue gas. In this paper, a series of novel Fe_xLa_yO_z/AC catalysts was prepared by the incipient wetness impregnation for NH₃-SCR denitrification reaction. The introduction of Fe-La bimetal oxides significantly improved the denitrification performance of activated coke at mid-high temperature, and 4% Fe_0.3La_0.7O_1.5/AC exhibited a superior NO_x conversion efficiency of 90.1% at 400 °C. The catalysts were further characterized by BET, SEM, XRD, Raman, EPR, XPS, FTIR, NH₃-TPD, H₂-TPR, et al., whose results showed that the perovskite-type oxide of LaFeO₃ and oxygen vacancies were produced on the catalysts’ surfaces during roasting. Fe-La doping enhanced the amount of acid sites (mainly Lewis and other stronger acid sites) and the content of multifarious oxygen species, which were beneficial for NO_x removal at mid-high temperature. Moreover, it was investigated that the effect of released CO from activated coke at mid-high temperature on the NO_x removal through the lifetime test, in which it was found that a large amount of CO produced by pyrolysis of activated coke could promote the NO_x removal, and long-term escaping of CO on the activated coke carrier did not have a significant negative impact on catalytic performance. The results of the TG-IR test showed that volatile matter is released from the activated coke while TG results showed that the weight loss rate of 4% Fe_0.3La_0.7O_1.5/AC only was 0.0015~0.007%/min at 300–400 °C. Hence, 4% Fe_0.3La_0.7O_1.5/AC had excellent thermal stability and denitrification performance to be continuously used at mid-high temperature. Finally, the mechanisms were proposed on the basis of experiments and characterization results.

     

Distribution,source, and environmental risk assessment of phthalate esters (PAEs) in water,suspended particulate matter,and sediment of a typical Yangtze River Delta City,China

Phthalates (PAEs) in drinking water sources such as the Yangtze River in developing countries had aroused widespread concern. Here, the water, suspended particulate matter (SPM), and sediment samples were collected from 15 sites in wet and dry seasons in Zhenjiang, for the determination of six PAEs (DMP, DEP, DIBP, DBP, DEHP, and DOP) using the solid-phase extraction (SPE) or ultrasonic extraction coupled with gas chromatography-mass spectrometry (GC-MS). The total concentrations of six PAEs (Σ₆PAEs) spanned a range of 2.65–39.31 μg L^?1 in water, 1.97–34.10 μg g^?1 in SPM, and 0.93–34.70 μg g^?1 in sediment. The partition coefficients (K_d1) of PAEs in water and SPM phase ranged from 0.004 to 3.36 L g^?1 in the wet season and from 0.12 to 2.84 L g^?1 in the dry season. K_d2 of PAEs in water and sediment phase was 0.001–9.75 L g^?1 in the wet season and 0.006–8.05 L g^?1 in the dry season. The dominant PAEs were DIBP, DBP, and DEHP in water and SPM, DIBP, DEHP, and DOP in sediment. The concentration of DBP in water exceeded the China Surface Water Standard. The discharge of domestic sewage and industrial wastewater might be the main potential sources of PAEs. The risk quotient (RQ) method used for the risk assessment revealed that DBP (0.01 < RQ < 1) posed a medium risk, while DIBP and DEHP (RQ > 1) posed a high environmental risk in water, DIBP (RQ > 1) also showed a high risk in sediment.

     

流化催化裂化烟气脱硫助剂的制备及其脱硫活性

采用溶胶-凝胶法制备锌铝助剂,该助剂于700℃焙烧后与流化催化裂化（FCC）催化剂进行机械混合,制得混合催化剂;在FCC烟气工业模拟装置上考察混合催化剂的脱硫活性,用混合催化剂的脱硫活性来反映锌铝助剂的脱硫性能。实验结果表明,氧化锌质量分数为10％的锌铝助剂的脱硫活性最佳,脱硫率达62．5％。采用红外光谱和X射线衍射（XRD）对锌铝助剂的脱硫机理进行了研究,红外分析结果表明,弱的L酸中心有利于锌铝助剂脱硫,XRD分析结果表明,锌铝助剂在锌铝尖晶石结构尚未完全形成时,存在较多的晶格缺陷,能够有效地吸附烟气中的SOx,将其转化为H2S。     

CO2资源化利用的现状及前景

介绍了CO2分离捕集最新工艺——电化学法、膜法、化学循环燃烧法的研究进展。评述分析了CO2的各种资源化应用前景：CO2气体用作生物碳源、辅助注射成型剂及有机物（如氨基甲酸酯、表面活性剂）合成原料等;液态CO2用于人造金刚石、热泵干燥、超临界CO2萃取及固体干冰冷喷射清洗等。CO2作为一种潜在的丰富碳源,应不断研发其新的应用领域,加快其工业化应用。