Effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria: Soot-ceria contact and interfacial oxygen evolution

Ceria is widely used as a catalyst for soot combustion, but effects of Zr substitution on the reaction mechanism is ambiguous. The present work elucidates effects of Zr substitution on soot combustion over cubic fluorite-structured nanoceria. The nanostructured CeO₂, Ce_0.92Zr_0.08O₂, and Ce_0.84Zr_0.16O₂ composed of 5–6 nm crystallites display T_m-CO2 (the temperature at maximum CO₂ yield) at 383, 355, and 375°C under 10 vol.% O₂/N₂, respectively. The size of agglomerate decreases from 165.5 to 51.9–57.3 nm, which is beneficial for the soot-ceria contact. Moreover, Zr increases the amount of surface oxygen vacancies, generating more active oxygen (O₂^? and O^?) for soot oxidation. Thus, the activities of Ce_0.92Zr_0.08O₂ and Ce_0.84Zr_0.16O₂ in soot combustion are better than that of CeO₂. Although oxygen vacancies promote the migration of lattice O^2?, the enriched surface Zr also inhibits the mobility of lattice O^2?. Therefore, the T_m-CO2 of Ce_0.84Zr_0.16O₂ is higher than that of Ce_0.92Zr_0.08O₂. Based on reaction kinetic study, soot in direct contact with ceria preferentially decomposes with low activation energy, while the oxidation of isolated soot occurs through diffusion with high activation energy. The obtained findings provide new understanding on the soot combustion over nanoceria.     

Comprehensive and high-resolution emission inventory of atmospheric pollutants for the northernmost cities agglomeration of Harbin-Changchun, China: Implications for local atmospheric environment management

Using a bottom-up estimation method, a comprehensive, high-resolution emission inventory of gaseous and particulate atmospheric pollutants for multiple anthropogenic sectors with typical local sources has been developed for the Harbin-Changchun city agglomeration (HCA). The annual emissions for CO, NOx, SO₂, NH₃, VOC_S, PM_2.5, PM₁₀, BC and OC during 2017 in the HCA were estimated to be 5.82 Tg, 0.70 Tg, 0.34 Tg, 0.75 Tg, 0.81Tg, 0.67 Tg, 1.59 Tg, 0.12 Tg and 0.26 Tg, respectively. For PM₁₀ and SO₂, the emissions from industry processes were the dominant contributors representing 54.7% and 49.5%, respectively, of the total emissions, while 95.3% and 44.5% of the total NH₃ and NOx emissions, respectively, were from or associated with agricultural activities and transportation. Spatiotemporal distributions showed that most emissions (except NH₃) occurred in November to March and were concentrated in the central cities of Changchun and Harbin and the surrounding cities. Open burning of straw made an important contribution to PM_2.5 in the central regions of the northeastern plain during autumn and spring, while domestic coal combustion for heating purposes was significant with respect to SO₂ and PM_2.5 emissions during autumn and winter. Furthermore, based on Principal Component Analysis and Multivariable Linear Regression model, air temperature, relative humidity, electricity and energy consumption, and the urban and rural population were optimized to be representative indicators for rapidly assessing the magnitude of regional atmospheric pollutants in the HCA. Such indicators and equations were demonstrated to be useful for local atmospheric environment management.     

蚯蚓对重金属污染土壤中铅的富集研究

蚯蚓在陆地生态系统中具有十分重要的功能,利用蚯蚓处理重金属污染土壤是一种新型的绿色生物技术。实验通过测定重金属污染土壤中不同铅浓度梯度下蚯蚓在培养期内对铅富集量的研究,结果表明：蚯蚓对铅有较强的富集作用,且随铅浓度的增加,蚯蚓体内的富集量也增加;单住质量蚯蚓培养期内吸收铅量与铅浓度梯度表现出极显著性差异,说明蚯蚓可以作为检测重金属污染土壤中铅的重要生物指标,论证了在重金属污染土壤动物修复中引入蚯蚓的可行性。     

Cd对不同形态漆酶修复DDT污染土壤的影响

研究了重金属Cd对游离漆酶和同定化反胶团漆酶修复土壤有机氯农药DDT污染的影响.结果表明.游离漆酶对土壤中DDT各组分均有不同程度降解,且均随着cd浓度的增大而降低,含量越高的组分降解率越高.受到Cd污染的影响也越大(P,P'-DDT>P,P'-DDD>0.P'-DDT>P,P'-DDE);当Cd浓度分别为0、0.5、1和2 mg·kg-1时,游离漆酶对土壤中DDT总量的降解率分别为50.68%、32.50%、14.92%和13.40%.固定化反胶团漆酶比游离漆酶能更有效地降解DDT,DDT降解率在无Cd和有Cd存在时(Cd浓度为0.5 mg·kg-1)分别提高20%和30%左右.     

毛细管离子色谱法测定空气中的氯化氢

以多孔玻板吸收管采样,用氢氧化钾-碳酸钠溶液吸收空气中的氯化氢(HCl),毛细管离子色谱法测定吸收液中的氯离子含量,根据采气量计算空气中的HCl含量。该方法灵敏度高,检出限低,结果准确,可避免其他阴离子及卤素和含卤酸盐离子的干扰,适用于环境空气中低含量HCl的测定。     

Distribution characteristics of poly- and perfluoroalkyl substances in the Yangtze River Delta

In this work, a method was developed and optimized for the analysis of polyfluoroalkyl and/or perfluoroalkyl substances(PFASs) content in surface water and sediment samples with high instrumental response and good separation. Surface water and sediment samples were collected from the Yangtze River Delta(YRD) to analyze the distribution characteristics of perfluoroalkyl carboxylic acids(PFCAs), perfluoroalkane sulfonic acids(PFSAs), perfluoroalkyl phosphonic acids(PFPAs), perfluoroalkyl phosphinic acids(PFPiAs), and polyfluoroalkyl phosphoric acid diesters(di PAPs). The results showed that the total concentrations of PFCAs and PFSAs in YRD varied from 31 to 902 ng/L. PFCAs(≥ 11 carbons) and PFSAs(≥ 10 carbons atoms) were not detected in any surface water samples. The mean concentrations of all PFCAs and PFSAs in surface water from the sampling areas decreased in the following order:Yangtze river(191 ng/L) ≈ Taihu lake(189 ng/L) Huangpu river(122 ng/L) ≈ Qiantang river(120 ng/L) Jiaxing urban river(100 ng/L). Strong significant(p 0.05) correlations between the concentrations of many of the compounds were found in the sampling areas, suggesting a common source for these compounds. Only perfluorooctanoic acid(PFOA) was observed in all sediment samples, at concentrations varying from 0.02 to 1.35 ng/g. Finally, detection rates of two di PAPs were only 8% and 10%, respectively and the concentration of di PAPs was two to three times lower compared to PFCAs and PFSAs.     

杭州湾表层海水营养盐分布特征及富营养化状况研究

根据2015年3月和8月杭州湾的海水质量监测数据,分析了该海域的营养盐分布特征以及富营养化状况,结果表明:杭州湾表层海水无机氮变化范围为0.36~4.22 mg/L,活性磷酸盐的含量范围为0.014~1.51 mg/L,化学需氧量含量范围为0.56~3.18 mg/L.该海域无机氮和活性磷酸盐超标严重,表层海水已处于重度富营养化状态,调查站位EI均大于1.该海域表层海水无机氮、活性磷酸盐、化学需氧量和富营养化指数高值区均与陆源入海口、养殖区、排污口等人类活动影响较大的区域有关.     

烟草废弃物快速堆肥过程中重金属Cd形态变化特征

以烟草废弃物为原料,活性土壤为载体建立堆体,研究重金属镉的形态变化,及堆肥过程中的动态变化规律。结果表明,烟草废弃物与活性土壤混合能快速腐熟。堆肥总质量下降,重金属镉含量相对增加。重金属镉的铁锰氧化态比例增加19%,有机结合态比例在堆肥升温阶段增加,腐熟后有所下降。残渣态比例大幅度上升,增加达到5倍,且在腐熟阶段增幅最大。说明堆肥处理有利于降低重金属镉的活性。     

压实黄土抗剪强度参数影响因素研究

为了进一步研究河南三门峡地区黄土抗剪强度的影响因素,采用应变控制式三轴仪对不同含水量、不同压实度下的重塑黄土进行不固结不排水三轴试验。试验结果表明:相同压实度下,随着含水量的增加,应力应变关系曲线由弱应变硬化向强应变硬化转变;粘聚力与内摩擦角均随含水量的增加而减小,粘聚力与含水量的变化呈明显负线性相关,内摩擦角与含水量无明显的相关性。相同含水量下,粘聚力与内摩擦角随压实度的增加而逐渐增大,且呈现出明显的指数相关。含水量对抗剪强度参数的影响比压实度大。对以上强度参数采用最小二乘法进行拟合,得出考虑含水率和压实度的抗剪强度相关关系式,能够较为准确的反映在某种试验条件下强度参数的变化规律,为实际工程应用和数值模拟提供依据。     

Effects of organic acids on Cd adsorption and desorption by two anthropic soils

The objective of this experiment was to study the effects of malic, tartaric, oxalic, and citric acid on the adsorption and desorption characteristics of Cd by two typical anthropic soils (lou soil and irrigation-silted soil) in North-west China. Cadmium adsorption and desorption were studied under a range of temperatures (25°C, 30°C, 35°C, 40°C), organic acid concentrations (0.5–5.0 mmol·L^-1), and pH values (2–8). The results showed that the Cd adsorption capacity of the lou soil was significantly greater than that of the irrigation-silted soil. Generally, Cd adsorption increased as the temperature increased. In the presence of NaNO₃, the adsorption of Cd was endothermic with ΔH values of 31.365 kJ·mol^-1 for lou soil and 28.278?kJ·mol^-1 for irrigation-silted soil. The endothermic reaction indicated that H bonds were the main driving force for Cd adsorption in both soils. However, different concentrations of organic acids showed various influences on the two soils. In the presence of citric acid, chemical adsorption and van der Waals interactions were the main driving forces for Cd adsorption rather than H bonds. Although the types of organic acids and soil properties were different, the effects of the organic acids on the adsorption and desorption of Cd were similar in the two soils. The adsorption percentage of Cd generally decreased as organic acid concentrations increased. In contrast, the adsorption percentage increased as the pH of the initial solution increased. The exception was that adsorption percentage of Cd increased slightly as oxalic acid concentrations increased. In contrast, the desorption percentage of Cd increased with increasing concentrations of organic acids but decreased as the initial solution pH increased.