新型铁铜铝三元复合氧化物除磷性能与机制研究

采用共沉淀法制备了一种新型铁铜铝三元复合氧化物吸附剂,系统研究了其对磷的吸附行为,并对吸附磷前后的吸附剂进行了表征.吸附实验结果表明,铁铜铝三元复合氧化物对磷具有优异的吸附去除效能,Freundlich吸附等温线模型能更好地拟合其对磷的吸附,最大吸附量为62.6 mg·g-1(pH=7.0),显著高于多数文献报道的磷吸附剂;吸附速率较快,吸附动力学更符合Elovich模型;溶液pH对磷吸附有一定影响,随着pH的升高,磷吸附量降低,离子强度则影响不大;共存阴离子对磷吸附具有抑制作用,影响的大小顺序为SiO_3~(2-)SO_4~(2-)CO_3~(2-)Cl~-,而共存阳离子Ca2+和Mg2+则对磷吸附略有促进作用.Zeta电位、红外谱图(FTIR)和X射线光电子能谱(XPS)表征分析表明,磷在铁铜铝三元复合氧化物表面发生了特性吸附,磷酸根主要通过取代复合氧化物表面的羟基形成内表面络合物而被吸附去除.溶出实验结果表明,当pH在5.0~8.5范围内,Fe~(3+)、Cu~(2+)、Al~(3+)的溶出量均较低.由此可知,铁铜铝三元复合氧化物是一种具有良好应用前景的除磷吸附剂.     

氧化亚铜在海水中释放速率研究

氧化亚铜是海洋防污涂料中重要的防污剂,防污剂中Cu²⁺释放速率将会显著影响其防污效果,同时海水中的Cu²⁺也影响海洋生物的生长,严格控制防污剂的释放速率对降低海洋生物的风险有重要意义.本研究使用人工海水对新型聚丙烯酸酯防污涂料中氧化亚铜释放速率进行测定,研究涂料构成及海水温度对Cu²⁺释放速率的影响.结果表明氧化亚铜在实验所用混合丙烯酸酯树脂涂料中能够快速实现稳定释放,达到良好防污效果.涂料中体质颜料用量影响涂料的孔隙,涂料颜料体积浓度（PVC）值介于0.136~0.154时,Cu²⁺释放速率适中.氧化亚铜在涂料中的Cu₂O含量高于26.9%时,有利于Cu²⁺长期稳定释放.海水温度升高,涂料Cu²⁺的释放速率将增加数倍.     

Water regime-nitrogen fertilizer incorporation interaction: Field study on methane and nitrous oxide emissions from a rice agroecosystem in Harbin, China

Water regime and nitrogen (N) fertilizer are two important factors impacting greenhouse gases (GHG) emission from paddy field, whereas their effects have not been well studied in cold region. In this study, we conducted a two-year field experiment to study the impacts of water regime and N fertilizer on rice yields and GHG emissions in Harbin, China, a cold region located in high latitudes. Our results showed that intermittent irrigation significantly decreased methane (CH₄) emission compared with continuous flooding, however, the decrement was far lower than the global average level. The N₂O emissions were very small when flooded but peaked at the beginning of the disappearance of floodwater. The N fertilizer treatments increased CH₄ emissions at low level (75kgN/ha). But both CH₄ and N₂O emissions were uninfluenced at the levels of 150kgN/ha and 225kgN/ha. Rice yields increased under intermittent irrigation and were highest at the level of 150kgN/ha. From our results, we recommended that the intermittent irrigation and 150kgN/ha as the ideal water regime-nitrogen fertilizer incorporation for this area to achieve low GHG emissions without impacting rice yields.     

Enhanced photocatalytic activity of rGO/TiO2 for the decomposition of formaldehyde under visible light irradiation

Due to the low concentration of indoor air contaminants,photocatalytic technology shows low efficiency for indoor air purification.The application of TiO_2 for photocatalytic removal of formaldehyde is limited,because TiO_2 can only absorb ultraviolet(UV) light.Immobilization of TiO_2 nanoparticles on the surface of graphene can improve the visible light photocatalytic activity and the adsorption capacity.In this study,rGO(reduced graphene oxide)/TiO_2 was synthesized through a hydrothermal method using titanium tetrabutoxide and graphene oxide as precursors,and was used for the degradation of low concentration formaldehyde in indoor air under visible light illumination.Characterization of the crystalline structure and morphology of rGO/TiO_2 revealed that most GO was reduced to rGO during the hydrothermal treatment,and anatase TiO_2 nanoparticles(with particle size of 15–30 nm) were dispersed well on the surface of the rGO sheets.rGO/TiO_2 exhibited excellent photocatalytic activity for degradation of formaldehyde in indoor air and this can be attributed to the role of rGO,which can act as the electron sink and transporter for separating photo-generated electron–hole pairs through interfacial charge transfer.Furthermore,rGO could adsorb formaldehyde molecules from air to produce a high concentration of formaldehyde on the surface of rGO/TiO_2.Under visible light irradiation for 240 min,the concentration of formaldehyde could be reduced to 58.5 ppbV.rGO/TiO_2 showed excellent moisture-resistance behavior,and after five cycles,r GO/TiO_2 maintained high photocatalytic activity for the removal of formaldehyde(84.6%).This work suggests that the synthesized rGO/TiO_2 is a promising photocatalyst for indoor formaldehyde removal.     

CuO/Ac催化过硫酸盐对模拟废水中苯酚的降解效果

含酚类废水所含有毒有害物质主要为苯酚,其排放量大,微溶于水且毒性较大,难以彻底处理.利用具有吸附性和催化性的CuO/Ac（活性炭负载CuO）催化过硫酸盐产生强氧化性的SO₄-·（硫酸根自由基）对模拟废水中苯酚进行降解,研究了不同因素（如反应温度、pH、水浴时间、CuO负载比、过硫酸盐投加量）对反应前、后模拟废水中苯酚和COD_Cr的去除率,并通过正交试验对这些因素进行了优化.结果表明:①过硫酸盐高级氧化法对苯酚的去除过程以氧化降解为主,在投加0.2 g负载比为1:5的CuO/Ac和过硫酸盐前提下,反应条件为pH 3、反应温度65℃,经过6 h的水浴反应,CuO/Ac催化过硫酸盐对于模拟废水中苯酚和COD_Cr的去除率分别可达到96.83%和91.90%.②通过正交试验得出,影响苯酚去除率大小的因素依次为反应温度>反应时间> pH,影响COD_Cr去除率大小的因素依次为反应温度> pH >反应时间.③在酸性、强碱性、高温条件下反应体系对苯酚的降解作用更明显,苯酚降解过程为先开环再进一步降解;相对于单独采用过硫酸盐和活性炭催化过硫酸盐法,采用活性炭负载CuO催化过硫酸盐法对模拟苯酚废水中苯酚具有去除率高、节省成本、处理速度快等优点.研究显示:在相同的试验设计情况下,应先考虑温度对反应的影响;在反应温度相同的条件下,根据对苯酚或对COD_Cr的去除率的不同要求,分别优先考虑反应时间、pH对试验的影响.      

氧化镁湿法烟气脱硫回收工艺的技术经济可行性初步分析

介绍了回收结晶硫酸镁的氧化镁湿法烟气脱硫工艺的基本工艺流程，在抛弃法脱硫系统上所作的工业试验证明了吸收液循环提浓MgSO4的可行性。参照工业硫酸镁生产工艺对130t／h燃煤锅炉烟气脱硫作了回收工艺的投资效益分析和整体工艺的经济性评价，结果表明回收工业硫酸镁具有良好的经济效益。     

用~(32)P后标记方法测定职业接触苯乙烯工人静脉血中DNA-环氧苯乙烯加合物

用~(32)P后标记方法,对一组22例接触苯乙烯的工人和8例未接触苯乙烯(空白)的工人进行测试,其静脉血中的淋巴细胞有4例(高浓度,大于40ppm)发现DNA-环氧苯乙烯加合物;而另外接触高浓度苯乙烯、低浓度苯乙烯和空白试样中,均未发现。在已测出的4例中,加合物形成水平为0.07—3.38加合物/10~7正常核酸,DNA的总损伤水平为5—9加合物/10~7正常核酸。 用小牛胸腺DNA、四种脱氧核苷3′-单磷酸分别与环氧苯乙烯进行体外反应,然后用~(32)P后标记法测定产物中的DNA加合物,初步确证有六种加合物及其衍生物存在,修饰位置是鸟苷碱基。并确证了其中三种加合物的化学结构,另外几种加合物的结构有待进一步鉴定。 ~(32)P后标记法测DNA加合物,灵敏度高达1加合物/10~(10)正常核酸,近于人体二倍体细胞基因水平(1.2×10~(10)碱基)。     

污泥膨胀形成机理及控制措施研究现状和进展

污泥膨胀现象在全球污水处理厂普遍存在,已成为制约活性污泥工艺发展的重大难题之一.本文总结了丝状细菌研究现状;重点阐述了当前引起污泥膨胀的主要机理;说明了基于这些机理的选择器控制理论;给出了主要的选择器类型.对当前关于污泥膨胀的研究进展和方向,分别从微生物和数学模型2个方面进行了讨论,最后,提出了一系列亟待解决的问题.     

华北地区旱田土壤氧化亚氮的排放

在１９９１－１９９３年间用封闭罩测定了对照田、施肥田Ｎ２Ｏ的排放量。结果表明，Ｎ２Ｏ通量显示出时、空变化规律。对照田，施尿素田和施混合肥田（尿素加有机肥）Ｎ２Ｏ排放量分别是１．０３±０．４ｋｇＮ／ｈｍ２ａ；１．９１±０．６ｋｇＮ／ｈｍ２ａ和２．１１±１．０ｋｇＮ／ｈｍ２ａ．尿素和混合肥释放Ｎ２Ｏ系数分别为０．２９％和０．３５％。由土壤含水量，土壤温度和速效氮浓度等土壤变量建立了Ｎ２Ｏ排放的统计模式。     

单分子层二氧化铈脱硫机理研究

单分子层二氧化铈可用于烟气中二氧化硫的脱除，文章研究了单分子层二氧化铈的硫化反应动力学。结果表明：硫化反应速率很高，且在反应初期基本保持不变；硫化增重在呈线性急剧诱惑 高后，逐渐趋于平稳，最后反应速率趋近为零。硫化反应处于扩散控制区，温度对反应速率影响很小，而二氧化硫的浓度对反应速率影响很大，还得到了硫化反应动力学方程。