铁氧化物多孔陶粒生物滴滤塔净化硫化氢气体

采用装有凹凸棒石基铁氧化物多孔陶粒作为填料的生物滴滤塔,进行了长期实验室H2S脱臭实验。结果表明,该生物滴滤塔H2S的进气浓度低于500 mg/m3 时,循环营养液喷淋量高于1.5 L/h,气体最佳停留时间为54.9 s,去除率在95 % 以上。代谢产物以SO42-为主,转化速率在52.42 g/(m3·d)左右。该滴滤塔系统可稳定而有效运行。生物相观察表明,滴滤塔填料表面附着大量微生物,铁氧化物陶粒具有化学和生物惰性,有利于微生物的附着。     

鱼菜共生系统氮素迁移转化的研究与优化

中国是世界上最大的水产养殖国,但是含有大量氮元素化合物的养殖废水对周围环境的污染已经成为影响该行业可持续发展的关键因素。鱼菜共生系统被认为是解决这一问题的有效途径。作为一种新兴的生态系统,目前对鱼菜共生系统中氮元素迁移转化规律的研究较少。通过对实验室规模的鱼菜共生系统进行研究,揭示系统内氮的迁移转化规律,掌握N2O的释放规律,同时尝试采用填料级配分层、添加硝化细菌等方式对系统进行优化。研究结果表明,投入系统的饵料中氮素以氨氮的形式被排出鱼体外后,在微生物作用下转化为亚硝酸盐氮及硝酸盐氮,进一步被植物吸收利用,提高了氮的利用效率。鱼菜共生系统以N2O形式释放的氮素约占氮素总输入的1.54%,与普通水产养殖相比,其N2O转化率没有明显增加。另外,采用填料级配分层以及添加硝化细菌等方法对系统进行优化,可促进系统内硝酸盐的积累,减少N2O释放,提高系统的经济效益和环境效益。     

Visible–light driven photocatalytic degradation of bisphenol-A using ultrasonically synthesized polypyrrole/K-birnessite nanohybrids: Experimental and DFT studies

Although manganese oxides are known for their semiconductor characteristics, the photocatalytic performance of conducting polymer intercalated K-Birnessite(K-Bi) has not been explored till date. With the view to design a visible light driven organic–inorganic hybrid photocatalyst for rapid degradation of Bisphenol A(BPA), the present work reports the ultrasound-assisted green synthesis of K-Bi/polypyrrole(Ppy) nanohybrids. The loading of Ppy in K-Bi was confirmed by thermogravimetric analysis while the formation of organic–inorganic hybrid was confirmed by infrared spectroscopy. K-Bi revealed a band gap of 2.8 e V while for the nanohybrids it was found to be ranging between 2.4 and 1.6 e V. X-ray diffraction studies confirmed partial intercalation of Ppy chains in the inter-layer space of K-Bi. High resolution transmission electron microscopy and scanning electron microscopy studies showed mixed morphology of K-Birnessite/Ppy nanohybrids. Rapid degradation of BPA was observed under visible irradiation in presence of K-Bi/Ppy nanohybrids and almost90% degradation of 20 mg/L BPA solution was achieved within 120 min. The degradation was found to follow pseudo-first order kinetics and the degraded fragments were identified using liquid chromatography-mass spectrometry. Degradation pathway was proposed based on density-functional theory calculations of fukui index predicting the radical easyattacking(f0) and(f-) sites in BPA.     

Ce-promoted Mn/ZSM-5 catalysts for highly efficient decomposition of ozone

Manganese oxides supported by ZSM-5 zeolite (Mn/ZSM-5) as well as their further modified by Ce promoter were achieved by simple impregnation method for ozone catalytic decomposition. The yCe20Mn/ZSM-5–81 catalyst with 8% Ce loading showed the highest catalytic activity at relative humidity of 50% and a space velocity of 360 L/(g × hr), giving 93% conversion of 600 ppm O₃ after 5 hr. Moreover, this sample still maintained highly activity and stability in humid air with 50%–70% relative humidity. Series of physicochemical characterization including X-ray diffraction, temperature-programmed technology (NH₃-TPD and H₂-TPR), X-ray photoelectron spectroscopy and oxygen isotopic exchange were introduced to disclose the structure-performance relationship. The results indicated that moderate Si/Al ratio (81) of zeolite support was beneficial for ozone decomposition owing to the synergies of acidity and hydrophobicity. Furthermore, compared with 20Mn/ZSM-5-81, Ce doping could enhance the amount of low valance manganese (such as Mn²⁺ and Mn³⁺). Besides, the Ce³⁺/Ce⁴⁺ ratio of 8Ce20Mn/ZSM-5-81 sample was higher than that of 4Ce20Mn/ZSM-5-81. Additionally, the synergy between the MnO_x and CeO₂ could easily transfer electron via the redox cycle, thus resulting in an increased reducibility at low temperatures and high concentration of surface oxygen. This study provides important insights to the utilization of porous zeolite with high surface area to disperse active component of manganese for ozone decomposition.     

Instream Large Wood: Denitrification Hotspots with Low N2O Production

We examined the effect of instream large wood on denitrification capacity in two contrasting, lower order streams — one that drains an agricultural watershed with no riparian forest and minimal stores of instream large wood and another that drains a forested watershed with an extensive riparian forest and abundant instream large wood. We incubated two types of wood substrates (fresh wood blocks and extant streambed wood) and an artificial stone substrate for nine weeks in each stream. After in situ incubation, we collected the substrates and their attached biofilms and established laboratory‐based mesocosm assays with stream water amended with ¹⁵N‐labeled nitrate‐N. Wood substrates at the forested site had significantly higher denitrification than wood substrates from the agricultural site and artificial stone substrates from either site. Nitrate‐N removal rates were markedly higher on woody substrates compared to artificial stones at both sites. Nitrate‐N removal rates were significantly correlated with biofilm biomass. Denitrification capacity accounted for only a portion of nitrate‐N removal observed within the mesocosms in both the wood controls and instream substrates. N₂ accounted for 99.7% of total denitrification. Restoration practices that generate large wood in streams should be encouraged for N removal and do not appear to generate high risks of instream N₂O generation.     

间接碘法测定氮氧化物的氧化度

在测定工业排放废气中氮氧化物的氧化度时,以间接碘法测定氮氧化物废气中的二氧化氮浓度,同时以中和滴定法测定氮氧化物浓度,从而计算氮氧化物的氧化度。氧化度测定的变异系数为4％以下。     

新疆机动车尾气中NOx排放特征分析及治理途径探讨

随着经济的快速发展和人民生活水平的提高,机动车保有量快速增长,城市中机动车尾气污染也日益突出,为更有效的控制机动车尾气污染,文章重点分析介绍了我区城市中机动车尾气中氮氧化物排放特征,并提出了控制对策和建议.     

Reductive decomposition of waste gypsum with SiO<Subscript>2</Subscript>, Al<Subscript>2</Subscript>O<Subscript>3</Subscript>, and Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> additives

From the point of view of a sustainable and environment-friendly society based on the recycling of material resources, it is preferable to utilize waste gypsum as a substitute for lime, which is currently produced by the calcination of limestone. In the present work, the reductive decomposition of CaSO₄ was investigated under an atmosphere of CO: 2 vol%, CO₂: 30 vol%, with N₂ as a carrier gas without and with the addition of SiO₂, Al₂O₃, or Fe₂O₃. It was found that the decomposition temperature of CaSO₄ was significantly reduced from 1673 K to 1223 K when only 5 wt% Fe₂O₃ was added to CaSO₄. In the case of the addition of SiO₂ or Al₂O₃ to CaSO₄, the decomposition temperature was reduced from 1673 K to 1623 K. This was due to the formation of composite oxides (calcium ferrite, calcium silicate, or calcium aluminate) during the reaction of CaSO₄ with the additives at a lower temperature. In addition, the formation of unfavorable product CaS was inhibited in the presence of 5 wt% Fe₂O₃, and this inhibition effect further increased as the addition of Fe₂O₃ was increased. In contrast, no significant effect on the inhibition of CaS formation was observed on the addition of SiO₂ or Al₂O₃.     

氧化铝表面处理对吸附腐殖酸的影响

采用酸、碱和金属盐表面修饰处理,影响氧化铝表面结构和成份分布,以达到提高吸附性能的目的。研究表明,经酸处理和酸性条件下的钙镁修饰处理的氧化铝,其对腐殖酸的吸附能力比Al-500分别提高32.3％和23.8％。同时,就改性氧化铝去除腐殖酸的影响条件、动力学、热力学性能进行了讨论。     

富氧条件下氢部分选择性催化还原NO研究

研制成功了低钯含量活性非均布Pd Al2 O3催化剂 ,实现了富氧条件下 ,氢部分选择性催化还原NO过程。实验表明在该催化剂上 ,低温、富氧条件下NO的转化率高达 80 %～ 10 0 %。室温下 (～ 2 0℃ ) ,NO对氢氧反应有强烈的抑制作用 ,氢氧反应进行后 ,NO还原反应开始明显进行 ,其与氢氧反应为竞争的平行反应