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排序方式: 共有99条查询结果,搜索用时 78 毫秒
1.
Yanke Yu Jiali Zhang Changwei Chen Chi He Jifa Miao Huirong Li Jinsheng Chen 《环境科学学报(英文版)》2020,32(5):237-245
CuSO_4/TiO_2 catalysts with high catalytic activity and excellent resistant to SO_2 and H_2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH_3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO_4/TiO_2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH_3,temperature-programmed reduction of H_2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO_4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO_4 changed surface reducibility of the catalyst and favored the process of NH_3 oxidation to nitrogen oxides(NO_x).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃) decreased largely. 相似文献
2.
Yanqin Ren Gehui Wang Jianjun Li Can Wu Cong Cao Jiayuan Wang Lu Zhang Fan Meng Hong Li 《环境科学学报(英文版)》2018,30(9):32-44
Size-resolved biogenic secondary organic aerosols(BSOA) derived from isoprene and monoterpene photooxidation in Qinghai Lake, Tibetan Plateau(a continental background site) and five cities of China were measured using gas chromatography/mass spectrometry(GC/MS). Concentrations of the determined BSOA are higher in the cities than in the background and are also higher in summer than in winter. Moreover, strong positive correlations(R2= 0.44–0.90) between BSOA and sulfate were found at the six sites,suggesting that anthropogenic pollution(i.e., sulfate) could enhance SOA formation,because sulfate provides a surface favorable for acid-catalyzed formation of BSOA. Size distribution measurements showed that most of the determined SOA tracers are enriched in the fine mode( 3.3 μm) except for cis-pinic and cis-pinonic acids, both presented a comparable mass in the fine and coarse( 3.3 μm) modes, respectively. Mass ratio of oxidation products derived from isoprene to those from monoterpene in the five urban regions during summer are much less than those in Qinghai Lake region. In addition, in the five urban regions relative abundances of monoterpene oxidation products to SOA are much higher than those of isoprene. Such phenomena suggest that BSOA derived from monoterpenes are more abundant than those from isoprene in Chinese urban areas. 相似文献
3.
水解酸化—厌氧工艺处理高浓度抗生素废水研究 总被引:10,自引:0,他引:10
研究了水解酸化与厌氧消化组合工艺处理高浓度抗生素废水,结果表明,水解酸化反应器最大CODcr容积负荷达到 16.84kg/m3·d,复合厌氧反应器CODcr容积负荷达到8.57kg/m3·d;系统进水SO42-浓度为1325mg/L,CODcr/SO42-值最低达到 3;CODCr与SO42-总去除率分别为75.5%和95.2%,对各种抑制物质和冲击负荷表现出很好的适应性。 相似文献
4.
采用产酸脱硫反应器进行连续流试验并配合静态试验 ,从群体生态学角度考察限制性生态因子———COD SO2 -4 比、硫酸盐负荷率 (Ns)、pH值、氧化还原电位 (ORP)和碱度 (ALK)的定量化对产酸脱硫生态系统的影响 .提出COD SO2 -4 比大于2 0 ,Ns 小于 7 5kg(SO2 -4 ) (m3·d) ,pH =6 0— 6 2 ,ORP =- 32 0— - 42 0mV ,ALK =15 0 0— 2 0 0 0mg L是维持硫酸盐还原菌(SRB)较高活性和生态系统稳定性的标志 ,硫酸盐去除率可达 80 %— 90 % 相似文献
5.
Yongfeng Ji Zidan Yuan Guoqing Zhang Xing Wu Xu M Jinru Lin Shaofeng Wang 《环境科学学报(英文版)》2023,35(2):31-41
An advanced cost-saving method of removal of high-As(Ⅲ) from SO4(-Ⅱ)-rich metallurgi cal wastewater has been developed by diluting the SO4(-Ⅱ) content with As(Ⅲ)-Cl(-Ⅰ)-rich metallurgical wastewater and then by the direct precipitation of As(Ⅲ) with Fe(Ⅲ) at pH2.3.As(Ⅲ) removal at various SO4(-Ⅱ)/Cl(-Ⅰ) molar ratios and temperatures was investigated The results showed that 65.2–98.2%of As(III) immobilization into solids occurred at the SO4(Ⅱ)/Cl(-Ⅰ) mo... 相似文献
6.
Zhen Bi Deqing Wanyan Xiang Li Yong Huang 《Frontiers of Environmental Science & Engineering》2020,14(3):38
7.
María-Vicenta Galiana-AleixandreJosé-Antonio Mendoza-Roca Amparo Bes-Piá 《Journal of Cleaner Production》2011,19(1):91-98
The use of large quantities of sulfuric acid and other sulfur-containing chemicals causes high sulfate concentrations in the wastewater of a tannery. The aim of this work was reducing the sulfate concentration in the final wastewater from a tannery. For that, firstly a study about the main sulfate sources in a tannery was carried out and the total sulfates load in the tannery wastewater was evaluated. Two measures for sulfates reduction were studied: the recycling of unhairing wastewater to the soaking drums and the reuse of the chromium sulfate from the tanning washing wastewater after its separation by nanofiltration (NF). The first measure proposed was studied experimentally in laboratory drums of 5 L of volume. Two series of experiments with different volumes of unhairing wastewater in the soaking bath were carried out. The quality of the final leather was evaluated by means of mechanical tests. NF experiments were carried out in a laboratory pilot plant with a spiral wounded membrane element. Concerning the results, the combination of 50% unhairing wastewater and 50% of fresh water was appropriate in order to obtain leather with an acceptable quality. Besides, it drove to a diminution of approximately 10% in the addition of sulfide in the unhairing. Related to the NF experiments, 97% of the sulfates were rejected by the membrane. The separated ions could be recycled to the tanning drums. The application of the two measures (firstly the recycling of the unhairing wastewater and secondly the NF of the tanning washing wastewater) drove to a reduction of 14.82 kg SO4−2 t−1 of raw hide. 相似文献
8.
Sulfate removal from waste chemicals by precipitation 总被引:3,自引:0,他引:3
Chemical oxidation using Fenton's reagent has proven to be a viable alternative to the oxidative destruction of organic pollutants in mixed waste chemicals, but the sulfate concentration in the treated liquor was still above the acceptable limits for effluent discharge. In this paper, the feasibility of sulfate removal from complex laboratory wastewaters using barium and calcium precipitation was investigated. The process was applied to different wastewater cases (two composite samples generated in different periods) in order to study the effect of the wastewater composition on the sulfate precipitation. The experiments were performed with raw and oxidized wastewater samples, and carried out according to the following steps: (1) evaluate the pH effect upon sulfate precipitation on raw wastewaters at pH range of 2-8; (2) conduct sulfate precipitation experiments on raw and oxidized wastewaters; and (3) characterize the precipitate yielded. At a concentration of 80 g L(-1), barium precipitation achieved a sulfate removal up to 61.4% while calcium precipitation provided over 99% sulfate removal in raw and oxidized wastewaters and for both samples. Calcium precipitation was chosen to be performed after Fenton's oxidation; hence this process configuration favors the production of higher quality precipitates. The results showed that, when dried at 105 degrees C, the precipitate is composed of hemidrate and anhydrous calcium sulfate ( approximately 99.8%) and trace metals ( approximately 0.2%: Fe, Cr, Mn, Co, Ag, Mg, K, Na), what makes it suitable for reuse in innumerous processes. 相似文献
9.
The ability of thermal activated peroxydisulfate (PS) of mineralizing phenol at 70 °C from contaminated waters is investigated. Phenol in concentrations of 10−4 to 5 × 10−4 M is quantitatively depleted by 5 × 10−3 to 10−2 M activated PS in 15 min of reaction. However, mineralization of the organic carbon is not observed. Instead, an insoluble phenol polymer-type product is formed. A reaction mechanism including the formation of phenoxyl radicals and validated by computer simulations is proposed. High molecular weight phenolic products are formed by phenoxyl radical H-abstraction reactions. This is not the case for the room temperature degradation of phenol by sulfate radicals where sulfate addition to the aromatic ring mainly leads to the generation of hydroxycyclohexadienyl radicals leading to hydroxybenzenes and oxidized open chain products. Therefore, a change in the reaction mechanism is observed with increasing temperature, and thermal activation of PS at 70 °C does not lead to the mineralization of phenol. Thus PS activation at 70 °C may be considered a potential method to reduce the load of phenol in polluted waters by polymerization. 相似文献