Autotrophic denitrification for nitrate and nitrite removal using sulfur-limestone

In the study, both nitrate and nitrite could be removed effectively using sulfur-limestone, and the bacteria involved in sulfur-based denitrification for nitrate and nitrite removal were of the same species.     

脱氮硫杆菌自养反硝化及其影响因素研究进展

简要回顾了近几十年来利用脱氮硫杆菌进行自养反硝化及其影响因素方面的研究成果,阐述了接种脱氮硫杆菌的自养反硝化系统的应用范围和主要影响因素的研究现状。其中对一些与自养反硝化应用及其影响因素相关的重要问题、近年来研究的热点问题,如硫磺颗粒粒径影响、硫磺/石灰石的体积比、进水硫化物/硝酸盐的摩尔比、水力停留时间、有毒物质的影响以及脱氮动力学模型的建立进行了重点分析。指出了利用脱氮硫杆菌进行自养反硝化目前存在的一些技术方面的问题及其解决途径,并对其今后的发展趋势和应用前景进行了展望。     

水体中硝酸盐氮同位素分析预处理方法研究现状

同位素分析技术测定硝酸盐氮的丰度来确定污染源,可以从根本上控制水体中硝酸盐氮的来源。稳定氮同位素的组成不同,氮的来源也不同。介绍了同位素分析法的基本原理及来源不同的硝酸盐氮的丰度值,同时阐述了国内外稳定氮同位素分析的几种预处理方法的适用条件和限制因素。提出了目前硝酸盐氮同位素分析预处理中存在的问题,并对未来发展方向做了综述。     

东海大气气溶胶中无机氮组分的分布特征

利用2006年11～12月、2007年2～3月及2008年5～6月在东海4个航次中采集的33个总悬浮颗粒物样品和7套Anderson分级样品,分析了其中NH 4+、NO 3-和NO 2-的浓度,探讨了东海气溶胶中氮组分的季节变化和粒径分布.气溶胶中NH 4+的浓度为2.6～646.9 nmol.m-3,冬、春季较高,夏季较低.NO 3-的浓度为5.5～281.5 nmol.m-3,冬季较高,春、夏季较低.NO 2-的浓度很低,0.5 nmol.m-3.气溶胶中氮组分的相对贡献具有一定的季节变化趋势,冬季NH 4+和NO 3-的贡献相当,春、夏季以NH 4+的贡献为主.NO 3-的粒径分布月变化明显,11～12月主要分布在2.1μm的细粒子上,2～3月、5～6月分别集中在1.1～4.7μm和2.1～7.0μm的粗粒子上.NH 4+的粒径分布无明显月季差异,均主要分布在1.1μm的细粒子上.后向轨迹分析表明气团的来源和迁移路径显著影响气溶胶中无机氮的分布.气团来自污染较重的陆源,无机氮在大气中的浓度(nmol.m-3)和在颗粒物中的浓度(μmol.g-1)均较高;气团来自清洁的海洋源,无机氮在大气中和颗粒物中的浓度均较低.气团起源自陆源但在海上经过长距离的迁移,则无机氮在大气中的浓度相对较低,在颗粒物中的浓度相对较高.     

2004～2009年我国典型陆地生态系统地下水硝态氮评价

利用中国生态系统研究网络（CERN）2004～2009年31个典型陆地生态系统38个浅层地下水井硝态氮（NO 3--N）的监测数据,评价我国典型陆地生态系统地下水NO 3--N污染状况.结果表明,农田（4.85 mg.L-1±0.42 mg.L-1）、绿洲农田（3.72mg.L-1±0.42 mg.L-1）、城市（3....     

广东省春季一次酸雨过程的数值模拟

采用WRF/Chem模式对2004年4月6—8日发生在广东省一次典型冷锋酸雨过程的气象场和污染物分布进行数值模拟,分析此次酸雨过程中致酸污染物SO2、NOx、硫酸盐气溶胶和硝酸盐气溶胶的主要分布特征,进而探讨此次酸雨的成因.结果表明,冷锋过境前,边界层高度较低,不利于污染物扩散,主要是局地排放致酸;冷锋过境形成了逆温层,污染物在逆温层内成片状均匀分布,使广东省出现大范围的酸雨.污染物浓度分布的模拟结果表明:SO2以本地源为主;NOx扩散范围较SO2广,分布更均匀;硫酸盐气溶胶和硝酸盐气溶胶6日主要分布在粤北,7日成大范围片状分布,与pH值的分布特征相似.     

Ce掺杂低钒V2O5-WO3/TiO2催化剂脱除烟气元素汞的研究

制备了Ce掺杂的低矾V₂O₅-WO₃/TiO₂催化剂,在模拟燃煤烟气条件下开展Hg⁰的脱除实验.结果表明该催化剂具有很好的Hg⁰脱除能力,在200～500℃的温度范围内能脱除烟气中95%的Hg⁰.催化剂表征结果表明,比表面积、 孔容和孔径与汞脱除能力没有显著相关性.XPS的结果表明,催化剂表面的Ce是以Ce⁴⁺的形式存在,有利于Hg⁰的脱除反应.抗硫抗水实验表明,H₂O会轻微抑制Hg⁰的脱除反应,主要原因是H₂O和Hg⁰在样品表面的竞争吸附;SO₂会促进Hg⁰的脱除反应,原因是SO₂能增加样品表面的酸吸附位且增加表面Hg⁰的吸附量.     

Poly[β-(1→4)-2-amino-2-deoxy-D-glucopyranose] based zero valent nickel nanocomposite for efficient reduction of nitrate in water

Chemical reduction of nitrate using metal nanoparticles has received increasing interest due to over-dependence on groundwater and consequence health hazard of the nitrate ion. One major drawback of this technique is the agglomeration of nanoparticles leading to the formation of large flocs. A low cost biopolymeric material, poly [β-(1 → 4)-2-amino-2-deoxy-D-glucopyranose] (β-PADG) obtained from deacetylated chitin was used as stabilizer to synthesize zero valent nickel (ZVNi) nanoparticles. The β-PADG-ZVNi nanocomposite was characterized using infra red (IR), UV-Vis spectrophotometric techniques and Scanning Electron Microscope (SEM). The morphology of the composite showed that β-PADG stabilized-ZVNi nanoparticles were present as discrete particles. The mean particle size was estimated to be (7.76 ± 2.98) nm and surface area of 87.10 m²/g. The stabilized-ZVNi nanoparticles exhibited markedly greater reactivity for reduction of nitrate in water with 100% conversion within 2 hr contact owing to less agglomeration. Varying the β-PADG-to-ZVNi ratio and the ZVNi-to-nitrate molar ratio generally led to a faster nitrate reduction. About 3.4-fold difference in the specific reaction rate constant suggests that the application of the β-PADG-stabilizer not only increased the specific surface area of the resultant nanoparticles, but also greatly enhanced the surface reactivity of the nanoparticles per unit area.     

竹林河岸带土壤反硝化脱氮效果模拟及机理研究

以太湖流域上游南苕溪流域农业区竹林河岸带土壤为研究对象,采用乙炔抑制法研究不同外源硝态氮（NO₃^--N）添加量(模拟添加NO₃^--N浓度分别为0、5和10 mg·L^-1的污水,分别用N0、N5和N10处理表示)对不同离水距离（0～3、3～6、6～12 m）、不同深度（0～10、10～20、20～40 cm）土壤反硝化速率的影响.结果表明,N0、N5和N10处理的土壤72 h内的反硝化速率均值分别为59.65、163.56和295.81μg·kg^-1·h^-1,不同处理间差异显著.N5和N10处理的土壤对外源NO₃^--N的脱氮率均值分别为0.45和0.51,且N5处理显著低于N10处理;土壤反硝化速率和对外源NO₃^--N脱氮率均随NO₃^--N添加量的增大而增加.土壤反硝化速率随离水距离的增加而降低,表层土壤的...     

Calorimetric behaviors of hydroxylamine and its salts caused by Fe(III)

The objective of this study is to obtain information on the calorimetric behaviors of aqueous solutions of hydroxylamine (HA), hydroxylamine chloride (HACl), and hydroxylamine nitrate(HAN) caused by different Fe(III) states (free Fe(III) from Fe(NH₄)(SO₄)₂, Fe(CN)₆³⁻, and Fe(EDTA)⁻). The calorimetric data were obtained with a small-scaled reaction calorimeter, Super-CRC.

In the mixing with Fe(III), HA showed the highest reactivity among three substrates. Free Fe(III) and Fe(EDTA)⁻ showed catalytic effects in the reactions. In the overall heat of reactions, Fe(EDTA)⁻ exceeded free Fe(III), which precipitated as Fe(OH)₃ and decreased the chances of interactions with HA. It was suggested that the generation of NH₃ had taken place in the process of reducing HA along with Fe(II) oxidation. Fe(CN)₆³⁻ was less reactive than free Fe(III) and Fe(EDTA)⁻.

The ability of masking Fe(III) was estimated for CyDTA. The HA including CyDTA had no exothermic peak; however, there was an endothermic peak of the heat flow at Fe(III) injection. CyDTA was found to have the ability to inhibit a violent exothermic reaction of HA.