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1.
为实现白洋淀芦苇的有效利用,以白洋淀淀区芦苇(白苇)为原料,以KOH、K2CO3为活化剂,综合考虑制备过程中的剂料比、浸渍时间、活化温度、活化时间等因素的影响,通过正交试验,以碘吸附值和亚甲蓝吸附值综合作为吸附性能高低的评价标准,进行活性炭制备方法研究。结果表明:在以KOH为活化剂、剂料比为4∶1、浸渍时间36 h、850℃下活化1 h的条件下,制备的芦苇基生物质活性炭碘吸附值最高,亚甲基蓝吸附值较高;以K2CO3为活化剂、剂料比为3∶1、浸渍时间12 h、900℃下活化2 h的条件下,制备的芦苇基生物质活性炭有最高的碘吸附值和对亚甲蓝具有良好的吸附性。制备的生物质活性炭碘吸附值均高于国家活性炭一级品标准(1 000 mg/g),具备一定的实用性。  相似文献   
2.
Sustainable use of natural resources would entail ensuring that derived economic benefits today do not undermine the welfare of generations to come. On this basis, this study examines the nexus between natural resource rents and carbon dioxide (CO2) emissions disaggregated into production and consumption-based (i.e., trade-adjusted) CO2 emissions for a selected panel of 45 developing and transition economies over the period 1995–2017. The empirical model also incorporates the impacts of population, affluence, and energy intensity. The results show that affluence increases production-based CO2 emissions by 1.407%, with the EKC's predicted inverted U-shaped curve only explaining consumption-based CO2 emissions. Economic reliance on natural resource rents and energy intensification contribute 0.022% and 0.766%, respectively, to CO2 emissions embedded in territorial production inventories and 0.035% and 0.583%, respectively, to CO2 emissions embedded in consumption inventories. The bootstrap non-causality test shows that historical data on each variable has significant predictive power for future CO2 emissions from both sources. The historical information about natural resource rents has significant predictive power over the future levels of affluence and energy intensity. Clearly, the results show that the environmental impact of natural resource rents is stronger when CO2 emissions are adjusted for trade and varies among the countries, with Bangladesh, Guinea, India, Malaysia, Mexico, Nigeria, Pakistan, Saudi Arabia, Vietnam, and Zimbabwe among the most affected countries. Overall, this study provides motivation for policies to keep the use of natural resources within sustainable limits.  相似文献   
3.
水源地土壤环境质量状况关乎其流域内居民生命健康安全,是生态环境保护研究中的热点科学问题.选择湘东北典型河源区,采集表层土壤样品共87件,通过GIS技术和潜在生态风险指数法研究了土壤重金属(Cd、Pb、Cr、Hg和As)的空间分布特征和潜在生态风险,并采用多元统计分析和正定矩阵因子分解(PMF)模型解释了其可能来源和贡献率.结果表明:①湘东北典型河源区土壤呈酸性,土壤重金属ω(Cd)、ω(Pb)、ω(Cr)、ω(Hg)和ω(As)平均值分别为0.20、41.07、130.51、0.29和11.63mg ·kg-1,对标背景值,除As外均有富集;②土壤重金属综合潜在生态风险为中等风险等级,其中Cr、Pb和As为轻微风险等级,Cd和Hg均为强风险等级;③土壤Cd和Pb具有同源性,主要来源于农业活动,Cr和As受生活垃圾排放和自然母质的双重影响,Hg主要来源于化石燃烧及交通运输;④生活垃圾排放源、自然母质源、化石燃烧及交通运输源和农业活动源对湘东北典型河源区土壤重金属的贡献率分别为21.36%、35.92%、19.30%和23.42%,人为源贡献率大于自然源.研究结果对湘东北典型河源区的污染防治、生态修复和美丽乡村建设具有参考价值.  相似文献   
4.
Given the speed at which humans are changing the climate, species with high degrees of endemism may not have time to avoid extinction through adaptation. We investigated through teleconnection analysis the origin of rainfall that determines the phylogenetic diversity of rainforest frogs and the effects of microclimate differences in shaping the morphological traits of isolated populations (which contribute to greater phylogenetic diversity and speciation). We also investigated through teleconnection analysis how deforestation in Amazonia can affect ecosystem services that are fundamental to maintaining the climate of the Atlantic rainforest biodiversity hotspot. Seasonal winds known as flying rivers carry water vapor from Amazonia to the Atlantic Forest, and the breaking of this ecosystem service could lead Atlantic Forest species to population decline and extinction in the short term. Our results suggest that the selection of morphological traits that shape Atlantic Forest frog diversity and their population dynamics are influenced by the Amazonian flying rivers. Our results also suggest that the increases of temperature anomalies in the Atlantic Ocean due to global warming and in the Amazon forest due to deforestation are already breaking this cycle and threaten the biodiversity of the Atlantic Forest hotspot.  相似文献   
5.
刘欣宇  卢江  孟璇  刘铮  宋鹏  李季  田光明 《环境科学》2023,44(8):4647-4654
收集整理1992年1月至2022年5月长江经济带地区长期定位施肥试验文献,提取并整合了其中农田土壤有机碳的资料.采用归一化处理和变化速率的分析方法,研究长期不同施肥措施下长江经济带地区农田土壤有机碳含量的总体变化,并比较3种耕作模式及不同土壤类型下土壤有机碳含量的变化差异,判断分析试验持续年限长短对土壤有机碳动态的影响.结果表明,在长期不同施肥措施下,我国长江经济带地区农田土壤有机碳含量整体呈上升趋势,无机氮肥磷肥配施(NP)、无机氮磷钾肥配施(NPK)、单独施用有机肥(O)和有机无机肥配施(NPKO)处理均能增加农田土壤的有机碳含量,其中以NPKO处理为最大,而单独施用无机氮肥(N)则会降低土壤有机碳含量.旱田、水田和水旱轮作农田土壤有机碳含量变化速率分别为0.22、 0.24和0.16g·(kg·a)-1,3种耕作模式在土壤固碳效果方面并无显著性差异.O和NPKO处理下所带来的有机碳相对快速增加效应在旱田土壤中的持续年限最高不超过28 a,而在水田及水旱轮作土壤中依然可以持续到28 a以上.在不同的土壤类型下,土壤有机碳含量的变化速率存在着一定的差异,平均有机...  相似文献   
6.
• Pore structure affects biologically activated carbon performance. • Pore structure determines organic matter (OM) removal mechanism. • Microbial community structure is related to pore structure and OM removal. Optimizing the characteristics of granular activated carbon (GAC) can improve the performance of biologically activated carbon (BAC) filters, and iodine value has always been the principal index for GAC selection. However, in this study, among three types of GAC treating the same humic acid-contaminated water, one had an iodine value 35% lower than the other two, but the dissolved organic carbon removal efficiency of its BAC was less than 5% away from the others. Iodine value was found to influence the removal of different organic fractions instead of the total removal efficiency. Based on the removal and biological characteristics, two possible mechanisms of organic matter removal during steady-state were suggested. For GAC with poor micropore volume and iodine value, high molecular weight substances (3500–9000 Da) were removed mainly through degradation by microorganisms, and the biodegraded organics (soluble microbial by-products,<3500 Da) were released because of the low adsorption capacity of activated carbon. For GAC with higher micropore volume and iodine value, organics with low molecular weight (<3500 Da) were more easily removed, first being adsorbed by micropores and then biodegraded by the biofilm. The biomass was determined by the pore volume with pore diameters greater than 100 μm, but did not correspond to the removal efficiency. Nevertheless, the microbial community structure was coordinate with both the pore structure and the organic removal characteristics. The findings provide a theoretical basis for selecting GAC for the BAC process based on its pore structure.  相似文献   
7.
分别于2013年10月和2014年2月、5月、7月在贵阳市城区3个环境空气质量监测国控点位(南明区市监测站、云岩区黔灵公园马鞍山和观山湖区贵阳一中)进行PM10、PM2.5样品采集,并对10种水溶性离子(SO42-、NO2-、NO3-、NH4+、Cl-、F-、Na+、K+、Mg2+、Ca2+)的含量进行了分析。结果表明,研究时段内,贵阳市3个点位PM10、PM2.5平均质量浓度分别为(64.8±25.5)、(46.6±21.2)μg/m3。其中,云岩区黔灵公园马鞍山点位的颗粒物浓度最低,南明区市监测站点位最高。3个点位PM2.5平均浓度与PM10平均浓度的比值为0.719,表明贵阳市城区PM10中,PM2.5占主导地位。水溶性离子分析显示,SO42-、NO2-、NO3-、NH4+、Cl-、F-、Na+、K+主要分布在PM2.5中,Mg2+、Ca2+主要分布在PM10中。3个点位PM10和PM2.5中的水溶性离子均表现为SO42-、NH4+、Ca2+浓度较大,F-、NO2-较小,表明3个点位的污染源总体相同,且水溶性离子占PM10、PM2.5含量的比例达33.6%~48.1%。贵阳市城区大气中的SO2转化率在5月、7月、10月较高,2月最低,主要是由于5月、7月、10月的高温、高湿、强辐射环境条件促进了SO2向SO42-的转化。阴阳离子平衡分析表明,贵阳市城区PM10、PM2.5呈现出偏碱性的特征。水溶性离子主成分分析表明,贵阳市城区PM10中的水溶性离子主要来源于城市扬尘、生物质燃烧尘、煤烟尘、建筑尘以及二次粒子,PM2.5中水溶性离子的来源与PM10较为相似。  相似文献   
8.
对2020年4月—2021年3月北京市建成区挥发性有机物(VOCs)的化学特征、污染来源及其对臭氧(O3)污染的影响进行了研究。结果显示:O3日最大8 h滑动平均值在臭氧季(4—9月)均值为134 μg/m3,是非臭氧季(10月至次年3月)均值(59.6 μg/m3)的2.2倍。臭氧季VOCs体积浓度均值为14.3×10-9,明显低于非臭氧季(21.1×10-9),可能与光化学反应速率和VOCs来源的季节性差异有关。臭氧生成潜势(OFP)贡献率排名前10位的物种在臭氧季和非臭氧季相似,均包括间/对-二甲苯、甲苯、乙烯、邻二甲苯、异戊烷、正丁烷、丙烯、反式-2-丁烯和1,2,4-三甲基苯,但排名有所差异,燃煤源特征明显的乙烯等物种在非臭氧季上升明显,与溶剂使用、油气挥发相关的间/对二甲苯、甲苯、异戊烷和正丁烷等物种在臭氧季上升明显。甲苯/苯的值和异戊烷/正戊烷的值在臭氧季明显高于非臭氧季,反映出机动车排放和油气挥发等在臭氧季影响突出,非臭氧季是燃煤影响显著。基于正交矩阵因子分解模型(PMF),臭氧季解析出机动车尾气排放(40.9%)、溶剂使用(20%)、油气挥发(16.4%)、工业排放(17.6%)和植物排放(5.1%)等5种污染源;非臭氧季解析出机动车尾气(38.9%)、燃烧源(26.3%)、工业排放(17.8%)和溶剂使用(17%)等4种污染源。  相似文献   
9.
• N-doped activated carbon was prepared for catalytic pyrolysis of walnut shell. • Alkylphenols were selectively produced from catalytic pyrolysis process. • The alkylphenols yield increased by 8.5 times under the optimal conditions. • Formation mechanism of alkylphenols was proposed. Alkylphenols are a group of valuable phenolic compounds that can be derived from lignocellulosic biomass. In this study, three activated carbons (ACs) were prepared for catalytic fast pyrolysis (CFP) of walnut shell to produce alkylphenols, including nitrogen-doped walnut shell-derived activated carbon (N/WSAC), nitrogen-doped rice husk-derived activated carbon (N/RHAC) and walnut shell-derived activated carbon (WSAC). Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) experiments were carried out to reveal the influences of AC type, pyrolytic temperature, and AC-to-walnut shell (AC-to-WS) ratio on the product distributions. Results showed that with nitrogen doping, the N/WSAC possessed stronger capability than WSAC toward the alkylphenols production, and moreover, the N/WSAC also exhibited better effects than N/RHAC to prepare alkylphenols. Under the catalysis of N/WSAC, yields of alkylphenols were significantly increased, especially phenol, cresol and 4-ethylphenol. As the increase of pyrolytic temperature, the alkylphenols yield first increased and then decreased, while high selectivity could be obtained at low pyrolytic temperatures. Such a trend was also observed as the AC-to-WS ratio continuously increased. The alkylphenols production achieved a maximal yield of 44.19 mg/g with the corresponding selectivity of 34.7% at the pyrolytic temperature of 400°C and AC-to-WS ratio of 3, compared with those of only 4.67 mg/g and 6.1% without catalyst. In addition, the possible formation mechanism of alkylphenols was also proposed with the catalysis of N/WSAC.  相似文献   
10.
Chlorinated ethenes such as trichloroethene (TCE), cis‐1,2‐dichloroethene (cis‐1,2‐DCE), and vinyl chloride along with per‐ and polyfluoroalkyl substances (PFAS) have been identified as chemicals of concern in groundwater; with many of the compounds being confirmed as being carcinogens or suspected carcinogens. While there are a variety of demonstrated in‐situ technologies for the treatment of chlorinated ethenes, there are limited technologies available to treat PFAS in groundwater. At a former industrial site shallow groundwater was impacted with TCE, cis‐1,2‐DCE, and vinyl chloride at concentrations up to 985, 258, and 54 µg/L, respectively. The groundwater also contained maximum concentrations of the following PFAS: 12,800 ng/L of perfluoropentanoic acid, 3,240 ng/L of perfluorohexanoic acid, 795 ng/L of perfluorobutanoic acid, 950 ng/L of perfluorooctanoic acid, and 2,140 ng/L of perfluorooctanesulfonic acid. Using a combination of adsorption, biotic, and abiotic degradation in situ remedial approaches, the chemicals of concern were targeted for removal from the groundwater with adsorption being utilized for PFAS whereas adsorption, chemical reduction, and anaerobic biodegradation were used for the chlorinated ethenes. Sampling of the groundwater over a 24‐month period indicated that the detected PFAS were treated to either their detection, or below the analytical detection limit over the monitoring period. Postinjection results for TCE, cis‐1,2‐DCE, and vinyl chloride indicated that the concentrations of the three compounds decreased by an order of magnitude within 4 months of injection, with TCE decreasing to below the analytical detection limit over the 24‐month monitoring period. Cis‐1,2‐DCE, and vinyl chloride concentrations decreased by over 99% within 8 months of injections, remaining at or below these concentrations during the 24‐month monitoring period. Analyses of Dehalococcoides, ethene, and acetylene over time suggest that microbiological and reductive dechlorination were occurring in conjunction with adsorption to attenuate the chlorinated ethenes and PFAS within the aquifer. Analysis of soil cores collected pre‐ and post‐injection, indicated that the distribution of the colloidal activated carbon was influenced by small scale heterogeneities within the aquifer. However, all aquifer samples collected within the targeted injection zone contained total organic carbon at concentrations at least one order of magnitude greater than the preinjection total organic carbon concentrations.  相似文献   
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