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71.
Manure is an impending source of carbon(C), sulfur(S) and water(H_2 O). Consequently,microbial populations utilize these constituents to produce methane(CH4), carbon dioxide(CO_2), greenhouse gases(GHGs), and hydrogen sulfide(H_2 S). Application of nanoparticles(NPs) to stored manure is an emerging GHG mitigation technique. In this study, two NPs: nano zinc oxide(nZnO) and nano silver(nAg) were tested in swine manure stored under anaerobic conditions to determine their effectiveness in mitigating gaseous emissions and total gas production. The biological sources of gas production, i.e., microbial populations were characterized via Quantitative Polymerase Chain Reaction(qPCR) analysis. Additionally, pH, redox, and VFAs were determined using standard methods. Each treatment of the experiment was replicated three times and NPs were applied at a dose of 3 g/L of manure. Also, headspace gas from all treatment replicates were analyzed for CH_4 and CO_2 gas concentrations using an SRI-8610 Gas Chromatograph and H_2 S concentrations were measured using a Jerome 631 X meter. Nanoparticles tested in this study reduced the cumulative gas volume by 16%–79% compared to the control. Among the NPs tested, only nZnO consistently reduced GHG concentrations by 37%–97%. Reductions in H_2 S concentrations ranged from 87% to97%. Gaseous reductions were likely due to decreases in the activity and numbers of specific gas producing methanogenic archaea and sulfate reducing bacterial(SRB)species. 相似文献
72.
Jun Li Aimin Li Yan Li Minhui Cai Gan Luo Yaping Wu Yechao Tian Liqun Xing Quanxing Zhang 《Frontiers of Environmental Science & Engineering》2022,16(4):47
73.
Yi Chen Shilong He Mengmeng Zhou Tingting Pan Yujia Xu Yingxin Gao Hengkang Wang 《Frontiers of Environmental Science & Engineering》2018,12(5):13
74.
邱琬钧 《环境监测管理与技术》1997,9(2):44-45
通过条件试验,对改良比浊法测定水中硫酸根方法进行了改进。检测限为0.16mg/L,对地面水,地下水,降水和废水的测定,相对标准差小于1.2%,加标回收率在95.9%-103.8%之间。 相似文献
75.
Sunita Verma O. Boucher H.C. Upadhyaya O.P. Sharma 《Atmospheric environment (Oxford, England : 1994)》2006,40(40):7953-7962
The tropospheric sulfate radiative forcing has been calculated using an interactive chemistry scheme in LMD-GCM. To estimate the radiative forcing of sulfate aerosol on climate, a consistent interaction between atmospheric circulation and radiation computation has been allowed in LMD-GCM. The model results indicate that the change in the sulfate aerosols number concentration is negatively correlated to the indirect radiative forcing. The model simulated annual mean direct radiative forcing ranges from −0.1 to −1.2 W m−2, and indirect forcing ranges from −0.4 to −1.6 W m−2. The global annual mean direct effect estimated by the model is −0.48 W m−2, and that of indirect is −0.68 W m−2. 相似文献
76.
《环境科学学报(英文版)》2023,35(4):545-555
Attention should be paid to the sulfate reduction behavior in a pressure-bearing leachate saturated zone. In this study, within the relative pressure range of 0–0.6 MPa, the ambient temperature with the highest sulfate reduction rate of 50°C was selected to explore the difference in sulfate reduction behavior in a pressure-bearing leachate saturated zone. The results showed that the sulfate reduction rate might further increase with an increase in pressure; however, owing to the effect of pressure increase, the generated hydrogen sulfide (H2S) could not be released on time, thereby decreasing its highest concentration by approximately 85%, and the duration extended to about two times that of the atmospheric pressure. Microbial community structure and functional gene abundance analyses showed that the community distribution of sulfate-reducing bacteria was significantly affected by pressure conditions, and there was a negative correlation between disulfide reductase B (dsrB) gene abundance and H2S release rate. Other sulfate reduction processes that do not require disulfide reductase A (dsrA) and dsrB genes may be the key pathways affecting the sulfate reduction rate in the pressure-bearing leachate saturated zone. This study improves the understanding of sulfate reduction in landfills as well as provides a theoretical basis for the operation and management of landfills. 相似文献
77.
78.
Madhubhashini Makehelwal Yuansong Wei Sujithra K. Weragod Rohan Weerasooriya 《环境科学学报(英文版)》2020,32(2):326-337
It has recently been proposed that recalcitrant dissolved organic carbon(DOC) in groundwater plays a potent etiological role in the peculiar distribution of chronic kidney disease of unknown etiology(CKDu).This study aims to elucidate the interactions of Ca~(2+)and SO_4~(2-)with a model organic fraction of humic acid(SHA) to determine the possible relationship of CKDu incidence with the DOC in drinking water.XPS and FT-IR methods respectively determined the surface functional groups and chemical composition of protonated dissolved organic carbon(HDOC) in a CKDu high-risk zone(HR) of Sri Lanka and in SHA.Higher surface C composition(87.9%) and lower O(11.4%) were observed for HDOC from the HR region than for SHA(C: 73.8%, O: 24.7%).Aromatic C with less Ocontaining functional groups was observed in HDOC.The IR band at 1170 cm~(-1) confirms the formation of organic sulfonate(C–SO_3~-) on SHA.A band at 1213 cm~(-1) due to organic sulfonate in HDOC from the CKDu HR region was also identified.The IR band at 866 cm~(-1) evidenced the formation of CaCO_3 on SHA above pH 7.4.XPS data confirmed the presence of sulfur oxidation states corresponding to SO_3~(2-)and SO_4~(2-)at 168.9 eV and 170.1 eV binding energies,respectively.The binding energies at 347 eV and 351 eV for Ca 2p_(3/2) and Ca 2p_(1/2) eV,respectively, confirmed the bidentate complexation of Ca~(2+)with COO-and sulfonate groups on SHA.The organic sulfonate formed is postulated as a uremic toxicant. 相似文献
79.
Fast screening compositions of PM2.5 by ATR-FTIR: Comparison with results from IC andOC/EC analyzers
Xu Yu Wei Song Qingqing Yu Sheng Li Ming Zhu Yanli Zhang Wei Deng Weiqiang Yang Zhonghui Huang Xinhui Bi Xinming Wang 《环境科学学报(英文版)》2018,30(9):76-88
Chemical speciation of fine particles or PM_(2.5) collected on filters is still a costly and timeconsuming task. In this study, filter-based PM_(2.5) samples were collected during November–December 2013 at four sites in Guangzhou, and the major components were fast screened(~7 min per filter sample) by Attenuated Total Reflectance(ATR)-Fourier Transform Infrared Spectroscopic(FTIR) in comparison with that measured by Organic carbon/Element carbon(OC/EC) analyzer and Ion Chromatography(IC). The concentrations of nitrate, ammonium, sulfate,primary organic carbon(POC) and secondary organic carbon(SOC) measured by OC/EC and IC analyzers were better correlated with their infrared absorption peak heights at 1320 cm~(-1) for nitrate, 1435, 3045 and 3215 cm~(-1) for ammonium, 615 cm~(-1) for sulfate, 690, 760 and 890 cm~(-1) for POC and 1640 and 1660 cm~(-1) for SOC respectively, during polluted days(PM_(2.5) 75 μg/m~3) than during clean days(PM_(2.5)≤ 75 μg/m~3). With the evolution of a haze episode during our field campaign, the concentrations of the major PM_(2.5) components displayed consistent variations with their infrared absorption peak heights, suggesting ATR-FTIR could be a fast and useful technique to characterize filter-based PM_(2.5) compositions particularly during pollution events although cautions should be taken when PM_(2.5) levels are low. Notably, elevated PM_(2.5) mass concentrations occurred with enhanced ratios of [NO_(-3)]/[SO_4~(2-)] and [NH~(+4)]/[SO_4~(2-)], implying that nitrogenous components play vital roles in the PM_(2.5) pollution events in the study region. 相似文献
80.
Effects of mussel dredging on sediment metabolism (oxygen uptake and sulfate reduction rates) and phosphorus dynamics (flux across sediment-water interface and sequential extraction) were examined in Limfjorden (Denmark) during spring (May) and summer (August). Sediment samples were taken during mussel dredging and in addition an experimental simulation of the dredging was performed to investigate short-term changes in phosphorus (P) dynamics. Iron-bound P was reduced by up to 2/3 in the surface layer in the dredging track (from 31 to 8?mmol?P?m?2), whereas the dissolved P-pools and less reactive particulate pools were not affected by dredging. Sediment oxygen consumption was enhanced immediately after dredging, but returned to the initial level after 4 days (20–40?mmol?m?2?d?1). The enhanced consumption was attributed to reoxidation of reduced compounds released during dredging. Sulfate reduction rates were high in the area (13–15?mmol?m?2?d?1) and sulfides competed with P for oxidized iron resulting in low iron-bound pools in the area (<4% of total P pools). Sulfate reduction rates were stimulated by the resuspension of sediments, especially in August, where a subsurface maximum was found, possibly due to a mixing of labile organic matter into these layers. In contrast sulfate reduction rates were reduced in the dredging track due to removal of labile organic matter from the surface layers. The loss of P during dredging was to some extent counteracted by regeneration of iron-bound P pools in the surface layers. The release of P due to mussel dredging was estimated to be in the same order of magnitude as the annual loading from the catchments and point sources to Limfjorden. 相似文献