Water pollution by antibiotics is an increasing concern, which may be addressed by advanced oxidation processes using sulfites as precursors of sulfate radicals (SO4·–), yet the efficiency of sulfite activation is limited. Here, we tested copper cobalt sulfide (CuCo2S4) to activate sulfite, based on the synergy among transition metals and the facilitation of transition metal redox circulation by reductive sulfur species. We analyzed CuCo2S4 structure by X-Ray photoelectron spectroscopy, and we studied the effect of pH and radical scavengers. Results show 90–100% abatement of tetracycline concentration at pH 8.0–10.0, with SO4·– and HO· as the main reactive radicals. This finding is explained by the accelerated redox recycling of copper and cobalt by sulfur, and by the synergetic effect between active cobalt and copper sites.
Rational synthesis of robust layered double hydroxides(LDHs) nanosheets for high-energy supercapacitors is full of challenges.Herein,we reported an ultrasonication-assisted strategy to eco-friendly fabricate NiFe-LDHs nanosheets for the enhanced capacitive behavior.The experimental results combined with different advanced characterization tools document that the utilization of ultrasonication has a profound effect on the morphology and thickness of the as-obtained NiFe-LDHs,alternatively affecti... 相似文献
Poly(hydroxamic acid)-poly(amidoxime) chelating ligands were synthesized from poly(methyl acrylate-co-acrylonitrile) grafted acacia cellulose for removing toxic metal ions from industrial wastewaters. These ligands showed higher adsorption capacity to copper (2.80 mmol?g−1) at pH 6. In addition, sorption capacities to other metal ions such as iron, zinc, chromium, and nickel were also found high at pH 6. The metal ions sorption rate (t1/2) was very fast. The rate of adsorption of copper, iron, zinc, chromium, nickel, cobalt, cadmium and lead were 4, 5, 7, 5, 5, 8, 9 and 11 min, respectively. Therefore, these ligands have an advantage to the metal ions removal using the column technique. We have successfully investigated the known concentration of metal ions using various parameters, which is essential for designing a fixed bed column with ligands. The wastewater from electroplating plants used in this study, having chromium, zinc, nickel, copper and iron, etc. For chromium wastewater, ICP analysis showed that the Cr removal was 99.8% and other metal ions such as Cu, Ni, Fe, Zn, Cd, Pb, Co and Mn removal were 94.7%, 99.2%, 99.9%, 99.9%, 99.5%, 99.9%, 95.6% and 97.6%, respectively. In case of cyanide wastewater, the metal removal, especially Ni and Zn removal were 96.5 and 95.2% at higher initial concentration. For acid/alkali wastewater, metal ions removing for Cd, Cr and Fe were 99.2%, 99.5% and 99.9%, respectively. Overall, these ligands are useful for metal removal by column method from industrial wastewater especially plating wastewater. 相似文献
In this study, a series of CuMgAl layered double oxides (CuMgAl-LDOs) were obtained via calcination of CuMgAl layered double hy-droxides (CuMgAl-LDHs) synthesised via a co-precipitation method. The results show that CuMgAl-LDO can be prepared using an optimal Cu:Mg:Al molar ratio of 3:3:2, NaOH:Na2CO3 molar ratio of 2:1, and calcination temperature of 600 °C. CuMgAl-LDO is a char-acteristic of mesoporous material with a lamellar structure and large specific surface area. The removal efficiency of sulfameter (SMD) based on CuMgAl-LDO/persulfate (PS) can reach>98%over a wide range of initial SMD concentrations (5–20 mg L-1). The best removal efficiency of 99.49%was achieved within 120 min using 10 mg L-1 SMD, 0.3 g L-1 CuMgAl-LDO, and 0.7 mmol L-1 PS. Kinetic analysis showed that the degradation of SMD was in accordance with a quasi-first-order kinetic model. The stability of the CuMgAl-LDO catalyst was verified by the high SMD removal efficiency (> 97% within 120 min) observed after five recycling tests and low copper ion leaching concentration (0.89 mg L-1), which is below drinking water quality standard of 1.3 mg L-1 permittable in the U.S. Radical scavenging experiments suggest that SO·4- is the primary active species participating in the CuMgAl-LDO/PS system. Moreover, our mechanistic investigations based on the radical scavenging tests and X-ray photoelectron spectroscopy (XPS) results indicate that Cu(II)–Cu(III)–Cu(II) circulation is responsible for activating PS in the degradation of SMD and the degradation pathway for SMD was deduced. Accordingly, the results presented in this work demonstrate that CuMgAl-LDO may be an efficient and stable catalyst for the activation of PS during the degradation of organic pollutants. ? 2020, Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communi-cations Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). 相似文献
Nitrous oxide (N2O) is a greenhouse gas that can be released during biological nitrogen removal from wastewater. N2O emission from a sequencing batch reactor (SBR) for biological nitrogen and phosphorus removal from wastewater was investigated, and the aims were to examine which process, nitrification or denitrification, would contribute more to N2Oemission and to study the effects of heterotrophic activities on N2O emission during nitrification. The results showed that N2O emission was mainly attributed to nitrification rather than to denitrification. N2O emission during denitrification mainly occurred with stored organic carbon as the electron donor. During nitrification, NaO emission was increased with increasing initial ammonium or nitrite concentrations. The ratio of N2O emission to the removed ammonium nitrogen (N2O- N/NH4-N) was 2.5% in the SBR system with high heterotrophic activities, while this ratio was in the range from 0.14% to 1.06% in batch nitrification experiments with limited heterotrophic activities. 相似文献
Dielectrophoresis (DEP) process could enhance the removal the Cd2+ and Pb2+ with less absorbent.The removal rates of both Cd2+ and Pb2+ increased with the increase of voltage.The overall removal rate of Cd2+ and Pb2+ in the binary system is higher than that of Cd2+ or Pb2+ in the single system.DEP could cause considerable changes of the bentonite particles in both surface morphology and microstructure. Dielectrophoresis (DEP) was combined with adsorption (ADS) to simultaneously and effectively remove Cd2+ and Pb2+ species from aqueous solution. To implement the process, bentonite particles of submicro-meter size were used to first adsorb the heavy metal ions. These particles were subsequently trapped and removed by DEP. The effects of the adsorbent dosage, DEP cell voltage and the capture pool numbers on the removal rate were investigated in batch processes, which allowed us to determine the optimal experimental conditions. The high removal efficiency, 97.3% and 99.9% for Cd2+ and Pb2+, respectively, were achieved when the ions are coexisting in the system. The microstructure of bentonite particles before and after ADS/DEP was examined by scanning electron microscopy. Our results suggest that the dielectrophoresis-assisted adsorption method has a high capability to remove the heavy metals from wastewater. 相似文献
Biochar, is a low-cost material that can be used as an alternative adsorbent for the removal of heavy metals. In this study, a low-cost and efficient adsorbent synthesised from Jatropha curcas seeds was used for the uptake of Cu2+ from aqueous solutions. The as-prepared adsorbent was characterised by scanning electron microscopy and Brunauer–Emmett–Teller analysis post calcination at 500 °C, its BET surface area and total pore volume were 39.62?m2?g?1 and 0.049?m3?g?1, respectively. Subsequently, the effects of initial pH of the solution, contact time, and adsorbent material dosage on the adsorption of Cu2+ by the prepared adsorbent were investigated. The as-prepared adsorbent exhibited a high performance, with a maximum adsorption amount of 32.895?mg?g?1 for Cu2+ at pH 5.0 and 25 °C, owing to the presence of ?OH, C=O, C–O, Si-O-Si, and O-Si-O on its surface. The predominant Cu2+ adsorption mechanism was assumed to be ion exchange. Notably, the Cu2+ adsorption could attain equilibrium within 90?min. In addition, the fact that the Langmuir model was a better fit than the Freundlich model for the isotherm data of Cu2+ adsorption by the as-prepared adsorbent suggested that the adsorption of Cu2+ was a monolayer adsorption process. 相似文献
Conventional biological removal of nitrogen and phosphorus is usually limited due to the lack of biodegradable carbon source, therefore, new methods are needed. In this study, a new alternative consisting of enhanced biological phosphorus removal (EBPR) followed by partial nitritationanammox (PN/A), is proposed to enhance nutrients removal from municipal wastewater. Research was carried out in a laboratory-scale system of combined two sequencing batch reactors (SBRs). In SBR1, phosphorus removal was achieved under an alternating anaerobic-aerobic condition and ammonium concentration stayed the same since nitrifiers were washed out from the reactor under short sludge retention time of 2–3 d. The remaining ammonium was further treated in SBR2 where PN/A was established by inoculation. A maximum of nitrogen removal rate of 0.12 kg N?m–3?d–1 was finally achieved. During the stable period, effluent concentrations of total phosphorus and total nitrogen were 0.25 and 10.8 mg?L–1, respectively. This study suggests EBPR-PN/A process is feasible to enhance nutrients removal from municipal wastewater of low influent carbon source.
• Synthesized few-layered MoS2 nanosheets via surfactant-assisted hydrothermal method.• Synthesized MoS2 nanosheets show petal-like morphology.• Adsorbent showed 93% of mercury removal efficiency.• The adsorption of mercury is attributed to negative zeta potential (-21.8 mV). Recently, different nanomaterial-based adsorbents have received greater attention for the removal of environmental pollutants, specifically heavy metals from aqueous media. In this work, we synthesized few-layered MoS2 nanosheets via a surfactant-assisted hydrothermal method and utilized them as an efficient adsorbent for the removal of mercury from aqueous media. The synthesized MoS2 nanosheets showed petal-like morphology as confirmed by scanning electron microscope and high-resolution transmission electron microscopic analysis. The average thickness of the nanosheets is found to be about 57 nm. Possessing high stability and negative zeta potential makes this material suitable for efficient adsorption of mercury from aqueous media. The adsorption efficiency of the adsorbent was investigated as a function of pH, contact time and adsorbent dose. The kinetics of adsorption and reusability potential of the adsorbent were also performed. A pseudo-second-order kinetics for mercury adsorption was observed. As prepared MoS2 nanosheets showed 93% mercury removal efficiency, whereas regenerated adsorbent showed 91% and 79% removal efficiency in the respective 2nd and 3rd cycles. The adsorption capacity of the adsorbent was found to be 289 mg/g at room temperature. 相似文献
Environmental Chemistry Letters - Contamination of waters by pharmaceuticals is a major health issue. Therefore, there is a need for efficient techniques to remove pharmaceutical pollutants. Here,... 相似文献
The synthesis of renewable chemical fuels from CO2 and H2O via photoelectrochemical(PEC) route reprensents a promising room-temperature approach for transforming greenhouse gas into value-added chemicals(e.g., syngas), but to date it has been hampered by the lack of efficient photocathode for CO2 reduction. Herein, we report efficient PEC CO2 reduction into syngas by photocathode engineering. The photocathode is consisting of a planar p-n Si junction f... 相似文献
• The coupling of oxidants with ZVI overcome the impedance of ZVI passive layer.• ZVI/oxidants system achieved fast and long-effective removal of contaminants.• Multiple mechanisms are involved in contaminants removal by ZVI/oxidant system.• ZVI/Oxidants did not change the reducing property of ORP in the fixed-bed system. Zero-valent iron (ZVI) technology has recently gained significant interest in the efficient sequestration of a wide variety of contaminants. However, surface passivation of ZVI because of its intrinsic passive layer would lead to the inferior reactivity of ZVI and its lower efficacy in contaminant removal. Therefore, to activate the ZVI surface cheaply, continuously, and efficiently is an important challenge that ZVI technology must overcome before its wide-scale application. To date, several physical and chemical approaches have been extensively applied to increase the reactivity of the ZVI surface toward the elimination of broad-spectrum pollutants. Nevertheless, these techniques have several limitations such as low efficacy, narrow working pH, eco-toxicity, and high installation cost. The objective of this mini-review paper is to identify the critical role of oxygen in determining the reactivity of ZVI toward contaminant removal. Subsequently, the effect of three typical oxidants (H2O2, KMnO4, and NaClO) on broad-spectrum contaminants removal by ZVI has been documented and discussed. The reaction mechanism and sequestration efficacies of the ZVI/oxidant system were evaluated and reviewed. The technical basis of the ZVI/oxidant approach is based on the half-reaction of the cathodic reduction of the oxidants. The oxidants commonly used in the water treatment industry, i.e., NaClO, O3, and H2O2, can be served as an ideal coupling electron receptor. With the combination of these oxidants, the surface corrosion of ZVI can be continuously driven. The ZVI/oxidants technology has been compared with other conventional technologies and conclusions have been drawn. 相似文献
Developing a suitable catalyst for the elimination of highly toxic carbonyl sulfide(COS) and hydrogen sulfide(H2S) is of great significance in terms of industrial safety and environmental protection. We demonstrate here the facile synthesis of graphitized 2D micro-meso-macroporous carbons by one-step carbonization of a mixture of urea and glucose at 700–900℃. The as-synthesized graphitized catalysts, designated as 2DNHPC-x(x = urea/glucose mass ratio), are endowed with an ultra-high c... 相似文献