Removal of arsenic(III,V) by a granular Mn-oxide-doped Al oxide adsorbent: surface characterization and performance

In order to remove arsenic (As) from contaminated water, granular Mn-oxide-doped Al oxide (GMAO) was fabricated using the compression method with the addition of organic binder. The analysis results of XRD, SEM, and BET indicated that GMAO was microporous with a large specific surface area of 54.26 m^2/g, and it was formed through the aggregation of massive Al/Mn oxide nanoparticles with an amorphous pattern. EDX, mapping, FTIR, and XPS results showed the uniform distribution of Al/Mn elements and numerous hydroxyl groups on the adsorbent surface. Compression tests indicated a satisfactory mechanical strength of GMAO. Batch adsorption results showed that As(V) adsorption achieved equilibrium faster than As(III), whereas the maximum adsorption capacity of As(III) estimated from the Langmuir isotherm at 25 °C (48.52 mg/g) was greater than that of As(V) (37.94 mg/g). The As removal efficiency could be maintained in a wide pH range of 3~8. The presence of phosphate posed a significant adverse effect on As adsorption due to the competition mechanisms. In contrast, Ca²⁺ and Mg²⁺ could favor As adsorption via cation-bridge involvement. A regeneration method was developed by using sodium hydroxide solution for As elution from saturated adsorbents, which permitted GMAO to keep over 75% of its As adsorption capacity even after five adsorption–regeneration cycles. Column experiments showed that the breakthrough volumes for the treatment of As(III)-spiked and As(V)-spiked water (As concentration = 100 μg/L) were 2224 and 1952, respectively. Overall, GMAO is a potential adsorbent for effectively removing As from As-contaminated groundwater in filter application.

     

Overview of surface measurements and spatial characterization of submicrometer particulate matter during the DISCOVER-AQ 2013 campaign in Houston,TX

The sources of submicrometer particulate matter (PM₁) remain poorly characterized in the industrialized city of Houston, TX. A mobile sampling approach was used to characterize PM₁ composition and concentration across Houston based on high-time-resolution measurements of nonrefractory PM₁ and trace gases during the DISCOVER-AQ Texas 2013 campaign. Two pollution zones with marked differences in PM₁ levels, character, and dynamics were established based on cluster analysis of organic aerosol mass loadings sampled at 16 sites. The highest PM₁ mass concentrations (average 11.6 ± 5.7 µg/m³) were observed to the northwest of Houston (zone 1), dominated by secondary organic aerosol (SOA) mass likely driven by nighttime biogenic organonitrate formation. Zone 2, an industrial/urban area south/east of Houston, exhibited lower concentrations of PM₁ (average 4.4 ± 3.3 µg/m³), significant organic aerosol (OA) aging, and evidence of primary sulfate emissions. Diurnal patterns and backward-trajectory analyses enable the classification of airmass clusters characterized by distinct PM sources: biogenic SOA, photochemical aged SOA, and primary sulfate emissions from the Houston Ship Channel. Principal component analysis (PCA) indicates that secondary biogenic organonitrates primarily related with monoterpenes are predominant in zone 1 (accounting for 34% of the variability in the data set). The relevance of photochemical processes and industrial and traffic emission sources in zone 2 also is highlighted by PCA, which identifies three factors related with these processes/sources (~50% of the aerosol/trace gas concentration variability). PCA reveals a relatively minor contribution of isoprene to SOA formation in zone 1 and the absence of isoprene-derived aerosol in zone 2. The relevance of industrial amine emissions and the likely contribution of chloride-displaced sea salt aerosol to the observed variability in pollution levels in zone 2 also are captured by PCA.

Implications: This article describes an urban-scale mobile study to characterize spatial variations in submicrometer particulate matter (PM₁) in greater Houston. The data set indicates substantial spatial variations in PM₁ sources/chemistry and elucidates the importance of photochemistry and nighttime oxidant chemistry in producing secondary PM₁. These results emphasize the potential benefits of effective control strategies throughout the region, not only to reduce primary emissions of PM₁ from automobiles and industry but also to reduce the emissions of important secondary PM₁ precursors, including sulfur oxides, nitrogen oxides, ammonia, and volatile organic compounds. Such efforts also could aid in efforts to reduce mixing ratios of ozone.     

Performance of IUCN proxies for generation length

One of the criteria used by the International Union for Conservation of Nature (IUCN) to assess threat status is the rate of decline in abundance over 3 generations or 10 years, whichever is longer. The traditional method for calculating generation length (T) uses age‐specific survival and fecundity, but these data are rarely available. Consequently, proxies that require less information are often used, which introduces potential biases. The IUCN recommends 2 proxies based on adult mortality rate, = α + 1/d, and reproductive life span, = α + z^*RL, where α is age at first reproduction, d is adult mortality rate, RL is reproductive life span, and z is a coefficient derived from data for comparable species. We used published life tables for 78 animal and plant populations to evaluate precision and bias of these proxies by comparing and with true generation length. Mean error rates in estimating T were 31% for and 20% for , but error rates for were 16% when we subtracted 1 year ( ), as suggested by theory; also provided largely unbiased estimates regardless of the true generation length. Performance of depends on compilation of detailed data for comparable species, but our results suggest taxonomy is not a reliable indicator of comparability. All 3 proxies depend heavily on a reliable estimate of age at first reproduction, as we illustrated with 2 test species. The relatively large mean errors for all proxies emphasized the importance of collecting the detailed life‐history information necessary to calculate true generation length. Unfortunately, publication of such data is less common than it was decades ago. We identified generic patterns of age‐specific change in vital rates that can be used to predict expected patterns of bias from applying .     

中部地区资源型城市城市化与生态环境动态耦合关系

通过构建城市化与生态环境耦合模型,利用中部地区37个资源型城市2005—2014年城市化系统和生态环境系统的30个指标数据,对城市化与生态环境耦合关系动态变化进行测度,并比较分析不同类型资源型城市城市化水平、生态环境水平及其二者耦合协调度的变化。结果表明:(1)2005以来人口城市化对资源型地区城市化综合水平的影响力减弱,社会城市化的影响力逐渐加大并趋于比较重要的地位。尽管资源条件对资源型城市的生态环境综合水平影响最大,但生态环境治理水平对资源型地区生态环境综合水平的影响力正变得日益重要。(2)各城市间城市化综合水平差异较大,而生态环境综合水平差异较小。自2005年以来城市化发展综合水平的城际差异无较大改变,但生态环境发展水平的城际差异正变得日趋缩小。位于山西省的资源型城市城市化综合水平和生态环境综合水平的变动较之其他省份更为显著。(3)中部地区资源型城市的协调类型处于勉强协调、初级协调和中级协调,并以初级协调型为主。2005以来中部地区多数资源型城市城市化与生态环境关系保持不变,关系恶化的资源型城市主要分布在安徽、江西和湖南,关系更为协调的资源型城市主要位于山西。(4)不同类型资源型城市的城市化综合水平差异显著,而生态环境综合水平差异并不明显。再生型和衰退型城市的耦合协调度水平较高,成熟型城市的耦合协调度较低。(5)城市化滞后仍是资源型城市城市化与生态环境关系不协调发展的主要原因。     

微生物燃料电池的专利技术综述

检索了微生物燃料电池在中国的发明专利文献,综述了微生物燃料电池在废水处理中的应用及与现有技术中其他水处理技术耦合的专利进展,并对其实际应用的前景进行了展望。     

KOH活化花生壳生物质炭对亚甲基蓝吸附性能研究

以花生壳生物质炭(P-BC)为原料,KOH为活化剂,采用化学活化法制得活化生物质炭(K-BC),通过考察对亚甲基蓝的吸附性能,研究了花生壳生物质炭的最佳活化条件,并利用N2吸附-脱附实验、SEM等对最佳活化条件下的生物质炭进行表征。结果表明,K-BC活化的最佳条件为碱炭比为1.5∶1,活化温度为800℃,活化时间为90 min,此时K-BC的比表面积达到597.93 m2/g,总孔容达到0.76 cm3/g。并考察了亚甲基蓝初始浓度、pH等对K-BC吸附亚甲基蓝的影响,随着初始浓度的增加,吸附平衡时间显著延长,亚甲基蓝去除率显著降低;当pH=6时,K-BC对亚甲基蓝的吸附量最大;K-BC对亚甲基蓝的吸附动力学曲线符合伪二阶动力学模型,吸附平衡时K-BC对亚甲基蓝的吸附能力为80~149.95 mg/g。     

肖四海不同渔业发展阶段的水环境特征分析

2006～2008年,对长江中游的一个浅水湖泊--肖四海进行了水质和水生植被研究,并结合历史资料分析了肖四海1987～2008年不同渔业发展阶段的水环境特征。研究结果表明：1987～2008年期间,该湖营养状况经历了中营养→富营养→中营养→富营养→中营养的变化过程,沉水植被经历了消亡→恢复→旺盛→衰退的演替过程,这种变化主要受不同阶段的渔业方式的影响。草食性鱼类和河蟹的过量放养、化肥的大量使用以及饵料的大量投放等不合理的渔业方式导致了水生植被的消亡和水体的富营养化,而合理的渔业方式不会对水体环境产生消极影响,并据此提出了长江中下游湖泊渔业可持续发展的建议     

棉花耐涝相关种质资源遗传多样性分析

为了解棉花耐涝相关种质资源的遗传多样性,选用均匀分布于棉花全基因组的145对引物,从中筛选出44对SSR引物对48份涝相关种质资源进行遗传多样性分析。结果表明,44对SSR引物在48份材料中共检测出170个等位基因变异,平均每个位点有386个。其中耐涝材料的位点多态信息含量(PIC)、每个位点的有效等位基因数(Ne)、基因型多样性(H′)分别为0632、1710 4和0393 7,涝敏感材料的PIC、Ne、H′分别为0628、1721 6和0399 4。耐涝材料和涝敏感材料的Jaccard相似性系数分别在0462~0925和0398~0845之间,遗传相似性系数总体平均值接近,但耐涝材料的变化幅度更大。用类平均法(UPGMA)聚类将48份材料分成2个类群。其中,第Ⅰ类包含39个品种,第Ⅱ类包含9个品种。大多数材料之间的遗传相似性系数较高,表明陆地棉耐涝相关种质资源遗传基础狭窄。本结果可为棉花耐涝育种亲本选配和相关机理研究提供基础资料     

Levels and distribution of Dechloranes in sediments of Lake Taihu,China

The occurrence and spatial distribution of dechloranes including mirex, dechlorane plus (DP), dechlorane (Dec) 602, Dec 603, and Dec 604 in surficial sediments of Lake Taihu were investigated in this study. The concentrations of mirex and DP ranged from below detection limit (BDL) to 1.29 ng g^?1 dw and 0.051 to 2.10 ng g^?1 dw, respectively. Dec 602, Dec 603, and Dec 604 on the other hand, were BDL in any of the samples. The contamination levels of DP were higher than that of Mirex at 21 of all 22 sampling sites. Levels of mirex and DP in the lake sediments were correlated when an extremely high mirex value was removed. Both mirex and DP levels were correlated with the amount of organic matters in the sediment samples. Spatial distribution of mirex and DP suggested that these two chemicals in the lake had similar input sources except for one site. Comparison to previously reported flame retardants’ levels in the sediments shows that DP levels were similar with the levels of tetrabromobisphenol A, hexabromocyclododecane but lower than PBDEs and organophosphates levels in Lake Taihu. The higher levels in the north-east part of Lake Taihu adjacent to two major cities: Wuxi and Suzhou, indicated that city effluent might be a major source for DP contamination in the lake.     

A comparison study on high-temperature water–gas shift reaction over Fe/Al/Cu and Fe/Al/Ni catalysts using simulated waste-derived synthesis gas

A comparative study on Fe/Al, Fe/Al/Cu, and Fe/Al/Ni catalysts in high-temperature water–gas shift reaction (HT–WGS) using simulated waste-derived synthesis gas has been carried out. The metal oxide (Cu and Ni) and aluminum incorporated Fe catalysts were designed to get highly active HT–WGS catalysts. Despite the high CO concentration in the simulated waste-derived synthesis gas, Fe/Al/Cu catalyst exhibited the highest CO conversion (84 %) and 100 % selectivity to CO₂ at a very high gas hourly space velocity (GHSV) of 40,057 h^?1. The outstanding catalytic performance is mainly due to easier reducibility, the synergy effect of Cu and Al, and the stability of the magnetite.