Synergistic effects of Cu species and acidity of Cu-ZSM-5 on catalytic performance for selective catalytic oxidation of n-butylamine

In this work, a series of Cu-ZSM-5 catalysts with different SiO₂/Al₂O₃ ratios (25, 50, 100 and 200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic degradation at 350°C over all Cu-ZSM-5 catalysts. Moreover, Cu-ZSM-5 (25) exhibited the highest selectivity to N₂, exceeding 90% at 350°C. These samples were investigated in detail by several characterizations to illuminate the dependence of the catalytic performance on redox properties, Cu species, and acidity. The characterization results proved that the redox properties and chemisorption oxygen primarily affect n-butylamine conversion. N₂ selectivity was impacted by the Brønsted acidity and the isolated Cu²⁺ species. Meanwhile, the surface acid sites over Cu-ZSM-5 catalysts could influence the formation of Cu species. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra was adopted to explore the reaction mechanism. The Cu-ZSM-5 catalysts are the most prospective catalysts for nitrogen-containing volatile organic compounds removal, and the results in this study could provide new insights into catalysts design for VOC catalytic oxidation.     

Photodegradation of Hexafluoropropylene Oxide Trimer Acid under UV Irradiation

As a novel alternative to traditional perfluoroalkyl substances (PFASs), including perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), hexafluoroproplyene oxide trimer acid (HFPO-TA) has been detected worldwide in surface water. Moreover, recent researches have demonstrated that HFPO-TA has stronger bioaccumulation potential and higher hepatotoxicity than PFOA. To treat these contaminants e.g. PFOA and PFOS, some photochemical techniques by adding exogenous substances had been reported. However, there is still no report for the behavior of HFPO-TA itself under direct UV irradiation. The current study investigated the photo-transformation of HFPO-TA under UV irradiation in aqueous solution. After 72 hr photoreaction, 75% degradation ratio and 25% defluorination ratio were achieved under ambient condition. Reducing active species, i.e., hydrated electrons and active hydrogen atoms, generated from water splitting played dominant roles in degradation of HFPO-TA, which was confirmed by different effects of reaction atmospheres and quenching experiments. A possible degradation pathway was proposed based on the products identification and theoretical calculations. In general, HFPO-TA would be transformed into shorter-chain PFASs, including hexafluoropropylene oxide dimer acid (HFPO-DA), perfluoropropionic acid (PFA) and trifluoroacetate (TFA). This research provides basic information for HFPO-TA photodegradation process and is essential to develop novel remediation techniques for HFPO-TA and other alternatives with similar structures.     

Polycyclic aromatic hydrocarbons in benthos of the northern Bering Sea Shelf and Chukchi Sea Shelf

Eighteen polycyclic aromatic hydrocarbons (PAHs) were detected in benthos collected onboard the ‘Snow Dragon’ in the Northern Bering Sea Shelf and Chukchi Sea Shelf during the 6^th Chinese National Arctic Research Expedition (CHINARE 2014). Σ₁₈PAHs for all biota samples ranged from 34.2 to 128.1 ng/g dry weight (dw), with the highest concentration observed in fish muscle (Boreogadus saida) samples close to St. Lawrence Island. The PAH composition pattern was dominated by the presence of lighter 3 ring (57%) and 2 ring (28%) PAHs, indicating oil-related or petrogenic sources as important origins of PAH contamination. Concentrations of alkyl-PAHs (1-methylnaphthalene and 2-methylnaphthalene) were lower than their parent PAH (naphthalene) in all biological tissue, and their percentage also decreased significantly (p<0.05) compared with those in the corresponding sediment. There were no significant relationships between PAH concentrations and trophic levels, which is possibly due to the combined results of the complex benthic foodweb in the subarctic/Arctic shelf region, as well as a low assimilation/effective metabolism for PAHs. According to toxic potency evaluation results from TCDD toxic equivalents (TEQs) and BaP-equivalent (BaPE) values, whelk (Neptunea heros) and starfish (Ctenodiscus crispatus) are two macroinvertebrate species showing relatively higher dioxin-like toxicity and carcinogenic risk.     

成都市施工扬尘排放特征研究

采用DustTRAK TM气溶胶（粉尘）监测仪对成都市112个不同类别的房建、市政工地施工扬尘进行测试,研究了不同类别施工扬尘的排放特征,分析了下风向扬尘浓度的变化趋势,并采用CALPUFF对成都市新都区某建筑工地的排放进行了模拟.结果表明：（1）成都市施工扬尘排放浓度约为0.13~2.91mg/m³,其中房建类施工平均浓度约为0.94mg/m³,高于市政施工;大型工地扬尘平均浓度约为0.61mg/m³,低于中型和小型工地;土方施工阶段平均浓度约为1.21mg/m³,远高于地基建设、主体建设、装饰阶段.（2）成都市施工扬尘呈现出高低浓度交替的周期性变化,其中房建工程土方施工阶段的高低浓度差值可达到0.6mg/m³以上.（3）施工扬尘在场界外下风向5~15m范围内会出现浓度增加的趋势,随后逐渐下降,在50m附近逐渐趋于稳定,稳定浓度介于0.1~0.2mg/m³.（4）CALPUFF模型能较好地从宏观角度来模拟成都地区施工扬尘的扩散趋势,但难以捕捉施工扬尘在下风向近距离的扩散特征.     

溢油胁迫下孔石莼碳氮稳定同位素的变化

为了研究溢油对海岸潮间带重要的大型绿藻孔石莼（Ulva Pertusa）的影响,本文探究了在180#燃料油的原油分散液（WAF）胁迫下,孔石莼的生长速率、叶绿素a以及碳氮稳定同位素的变化。在低WAF浓度（1.43 mg/L、2.87 mg/L和4.30 mg/L）胁迫下,对孔石莼的生长具有促进作用,生长速率均高于对照组,同时叶绿素a和碳氮稳定同位素均呈现上升的趋势;而高浓度WAF（5.72 mg/L和7.17 mg/L）会抑制藻类生长,导致生长速率低于对照组,而叶绿素a含量却高于对照组,孔石莼的δ15N和δ13C相比对照组偏负。对于孔石莼来说,C、N稳定同位素变化的趋势比叶绿素a更明显,这表明在溢油胁迫下,孔石莼的C、N稳定同位素能够更好更快速地评价溢油胁迫毒性大小,因此可以作为海洋环境监测和评价的一种新手段。     

Well-to-wheels greenhouse gas and air pollutant emissions from battery electric vehicles in China

Mitigation and Adaptation Strategies for Global Change - Electric vehicles (EVs) play a crucial role in addressing climate change and urban air quality concerns. China has emerged as the global...     

ICP——AES法在第二级观测As189.042nm分析线的干扰图

用ICP──AES法获得Ag、Al、Ba、Cr、Fe、Mg、Ni、Ph筹8个元素对As189．042×2nm分析线的干扰图，并测定了干扰程度。实验结果表明；浓度为As含量100倍的Ag、Ba、Fe、Mg、Ni、Ph对As分拆线几乎没有影响，而浓度为As含量100倍的Al和Cr对As分析线有一定的干扰．提出了校正和消除Al、Cr干扰的一些方法。     

Heavy metals in water bodies purified by suspended substrate of rivers

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淮北煤中12种有害微量元素在煤及其灰中的分布特征

为了解有害微量元素在各煤层中的分布与变化规律,以及在煤燃烧后的煤灰中所发生的迁移与富集情况,采集了淮北煤田不同煤层、不同深度的15个煤样,采用中子活化法对其原煤及灰分中的12 种微量元素(Ag, As,Ba, Co, Cr, Cu, Mn, Mo, Sb, Th, U, V)进行了测试。结果显示:绝大部分有害微量元素的含量都处于n×10 6到n×10 5数量级范围内,不同煤层或同一煤层不同部位中微量元素的含量分布不同;与全国和华北煤中有害微量元素的(平均)含量相比,除Mn低于全国和华北的平均值外,As、Co、Mo、Sb、Th、U与之相近,而Ag、Ba、Cr、Cu、V高于全国和华北煤中的平均值;12种微量元素均在灰分中有所富集,而且富集能力序列为:Cu>Cr>Mn>Mo>Co>Ba>V>Th>As>U>Sb。