Piezocatalytic removal of water bacteria and organic compounds: a review

Environmental Chemistry Letters - In the context of climate change, freshwater shrinkage and industrialization, human diseases are increasing due to water pollution by toxic chemicals and...     

Design of polymeric carbon nitride-based heterojunctions for photocatalytic water splitting: a review

Environmental Chemistry Letters - Developing high-efficiency and stable photocatalysts able to accomplish spontaneous overall water splitting, without using sacrificial agents, is the ultimate goal...     

High Cu removal from water using water hyacinth fixed on alginate

The occurrence of toxic metals in waters is a major health issue. Polluted waters can be cleaned by biosorption, which uses organisms such as algae, bacteria, fungi and plants that adsorb metals. In particular, water hyacinth—Eichhornia crassipes—is a promising biosorbent. Here we tested novel alginate-immobilised water hyacinth beads for the removal of Cu from aqueous solutions. Results show that successful service and regeneration continuous cycles were performed using a packed-bed, flow-through column of fixed internal diameter 1.2 cm, at room temperature and pH 5.1, with variation in initial metal concentration, bed depth and flow rate. The eluant used was 1 % w/v CaCl₂ acidified at pH 3. A concentration factor of 12 and elution efficiency up to 98 % were observed in five service and regeneration cycles performed. The equilibrium adsorption capacity of Cu remained almost constant at about 29 mg/g. To conclude, we show for the first time that alginate-immobilised water hyacinth beads can uptake and adsorb Cu very efficiently in a continuous-flow mode, hence highlighting their great potential for removal of toxic metals from aquatic environments.     

Complexing agents for metal removal using ultrafiltration membranes: a review

Environmental Chemistry Letters - Water pollution by human activities is major issue. In particular, toxic metals are of particular concern, thus calling for advanced methods to remove metals from...     

Methods for selenium removal from contaminated waters: a review

Environmental Chemistry Letters - Worldwide contamination of waters by metals, metalloids, and organometallic pollutants is a major health issue. In particular, the occurrence of the selenium...     

硅酸钙处理富营养化湖水中氨氮的实验研究

湖泊的富营养化问题日益严重,已给人类的生产、生活带来了极大的危害.而氨氮废水的大量排放,使原本恶化的湖泊水雪上加霜.为了去除富营养化湖水中氨氮,研究了硅酸钙对氨氮的吸附性能.经检测可知水样中氨氮的质量浓度为1.12 mg?L-1,实验结果表明,用粒径大小为100目的硅酸钙吸附剂处理100 mL的水样,当投加量为1.0 g,pH为8,震荡时间为60 min时吸附达到平衡,硅酸钙对富营养化湖水中氨氮的去除率达到81.67%;其吸附等温线符合Langmuir和Freundlich吸附等温式,线性相关系数分别为0.9639和0.9793,最大吸附量为6.60 mg?g-1;由此可见硅酸钙能够很好地吸附富营养化水体中的氨氮.     

High removal of nitrogen and phosphorus from black-odorous water using a novel aeration-adsorption system

Black-odorous waters are an increasingly common phenomenon characterized by excessive levels of nutrients, the formation of metal sufide precipitates, volatile sulfurous compounds, low dissolved oxygen and high chemical oxygen demand. Black-odorous waters frequently occur in lake and river systems where inputs have restricted circulation. The key remediation issue is the removal of nitrogen and phosphorus. Here, we present a novel aeration-adsorption system using fiber balls and we study treatment parameters and removal mechanism. Kinetics and changes of the solid phase were followed using Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. Results show complete removal of ammonia N, initially at 31 mg/L, and 92.8% removal of total nitrogen, initially at 29 mg/L, after a 24 h reaction time at pH 9.67. At pH 5.67 and 9.67, total phosphorus and phosphate could be significantly reduced by 90–92% at 3.2–5.2 mg/L after 24 h. Treatment met China’s integrated wastewater discharge standards, demonstrating an effective and robust treatment capability. First-order and second-order kinetic models provided a good fit to the treatment data, indicating physical and chemical adsorption were involved in the treatment reactions. The reaction mechanism involved hydrogen substitution and binding to oxygen. These results present a cost effective and robust approach for the removal of N and P from black, odorous water, providing opportunity to abate environmental contamination.

     

Technologies for pollutant removal and resource recovery from blackwater: a review

● Blackwater is the main source of organics and nutrients in domestic wastewater. ● Various treatment methods can be applied for resource recovery from blackwater. ● Blackwater treatment systems of high integration and efficiency are the future trend. ● More research is needed for the practical use of blackwater treatment systems. Blackwater (BW), consisting of feces, urine, flushing water and toilet paper, makes up an important portion of domestic wastewater. The improper disposal of BW may lead to environmental pollution and disease transmission, threatening the sustainable development of the world. Rich in nutrients and organic matter, BW could be treated for resource recovery and reuse through various approaches. Aimed at providing guidance for the future development of BW treatment and resource recovery, this paper presented a literature review of BWs produced in different countries and types of toilets, including their physiochemical characteristics, and current treatment and resource recovery strategies. The degradation and utilization of carbon (C), nitrogen (N) and phosphorus (P) within BW are underlined. The performance of different systems was classified and summarized. Among all the treating systems, biological and ecological systems have been long and widely applied for BW treatment, showing their universality and operability in nutrients and energy recovery, but they are either slow or ineffective in removal of some refractory pollutants. Novel processes, especially advanced oxidation processes (AOPs), are becoming increasingly extensively studied in BW treatment because of their high efficiency, especially for the removal of micropollutants and pathogens. This review could serve as an instructive guidance for the design and optimization of BW treatment technologies, aiming to help in the fulfilment of sustainable human excreta management.     

Occurrence,toxicity and adsorptive removal of the chloramphenicol antibiotic in water: a review

Chloramphenicol is a broad-spectrum bacterial antibiotic used against conjunctivitis, meningitis, plague, cholera, and typhoid fever. As a consequence, chloramphenicol ends up polluting the aquatic environment, wastewater treatment plants, and hospital wastewaters, thus disrupting ecosystems and inducing microbial resistance. Here, we review the occurrence, toxicity, and removal of chloramphenicol with emphasis on adsorption techniques. We present the adsorption performance of adsorbents such as biochar, activated carbon, porous carbon, metal–organic framework, composites, zeolites, minerals, molecularly imprinted polymers, and multi-walled carbon nanotubes. The effect of dose, pH, temperature, initial concentration, and contact time is discussed. Adsorption is controlled by π–π interactions, donor–acceptor interactions, hydrogen bonding, and electrostatic interactions. We also discuss isotherms, kinetics, thermodynamic data, selection of eluents, desorption efficiency, and regeneration of adsorbents. Porous carbon-based adsorbents exhibit excellent adsorption capacities of 500–1240 mg g^?1. Most adsorbents can be reused over at least four cycles.

     

Clay mineral adsorbents for heavy metal removal from wastewater: a review

Environmental Chemistry Letters - Heavy metal pollution such as water contamination by Pb, Hg, Cu, Cd and Cr ions is induced by rapid urbanization and industrialization and is a major threat to...     

Recent advances in antimony removal using carbon-based nanomaterials: A review

• The synthesis and physicochemical properties of various CNMs are reviewed. • Sb removal using carbon-based nano-adsorbents and membranes are summarized. • Details on adsorption behavior and mechanisms of Sb uptake by CNMs are discussed. • Challenges and future prospects for rational design of advanced CNMs are provided. Recently, special attention has been deserved to environmental risks of antimony (Sb) element that is of highly physiologic toxicity to human. Conventional coagulation and ion exchange methods for Sb removal are faced with challenges of low efficiency, high cost and secondary pollution. Adsorption based on carbon nanomaterials (CNMs; e.g., carbon nanotubes, graphene, graphene oxide, reduced graphene oxide and their derivatives) may provide effective alternative because the CNMs have high surface area, rich surface chemistry and high stability. In particular, good conductivity makes it possible to create linkage between adsorption and electrochemistry, thereby the synergistic interaction will be expected for enhanced Sb removal. This review article summarizes the state of art on Sb removal using CNMs with the form of nano-adsorbents and/or filtration membranes. In details, procedures of synthesis and functionalization of different forms of CNMs were reviewed. Next, adsorption behavior and the underlying mechanisms toward Sb removal using various CNMs were presented as resulting from a retrospective analysis of literatures. Last, we prospect the needs for mass production and regeneration of CNMs adsorbents using more affordable precursors and objective assessment of environmental impacts in future studies.     

Mechanisms of arsenic removal from water

In this review paper, various methods for arsenic removal from water have been described by explaining the related mechanisms of each methods. Advantages and drawbacks were discussed. Membrane methods were suggested as reliable methods for elimination of arsenic from water in addition to other conventional separation methods.     

Pollution magnet: nano-magnetite for arsenic removal from drinking water

Arsenic contamination in groundwater is a severe global problem, most notably in Southeast Asia where millions suffer from acute and chronic arsenic poisoning. Removing arsenic from groundwater in impoverished rural or urban areas without electricity and with no manufacturing infrastructure remains a significant challenge. Magnetite nanocrystals have proven to be useful in arsenic remediation and could feasibly be synthesized by a thermal decomposition method that employs refluxing of FeOOH and oleic acid in 1-octadecene in a laboratory setup. To reduce the initial cost of production, $US 2600/kg, and make this nanomaterial widely available, we suggest that inexpensive and accessible “everyday” chemicals be used. Here we show that it is possible to create functional and high-quality nanocrystals using methods appropriate for manufacturing in diverse and minimal infrastructure, even those without electricity. We suggest that the transfer of this knowledge is best achieved using an open source concept.     

Hydrogels for the removal of the methylene blue dye from wastewater: a review

Environmental Chemistry Letters - Water pollution is a major environmental issue with the rapid development of industry. Therefore, advanced technologies and materials are needed to remove...     

Photoelectrochemical water splitting using post-transition metal oxides for hydrogen production: a review

Environmental Chemistry Letters - Dihydrogen (H2), commonly named ‘hydrogen,’ is considered as a promising renewable fuel that does not emit carbon dioxide upon combustion. Nonetheless,...     

Detection and removal of heavy metal ions: a review

Environmental Chemistry Letters - In aqueous systems, heavy metal ions, when present in excess than permissible limits, are dangerous for human beings and aquatic life. Heavy metals cannot be...     

Optimisation of bisphenol A removal from water using chemically modified pine bark and almond shell

The ability of pine bark and almond shells to remove bisphenol A (BPA) from aqueous solutions was evaluated. Samples of these traditional agro-forestry by-products were milled, sieved into different particle size fractions (0.10–0.15 and 1.5–2.0 mm) and submitted to two different types of treatment. Sorption experiments were conducted in a batch system at room temperature and natural pH. Sorption equilibrium was attained after 48 h for all systems under study. Bisphenol A was adsorbed more effectively on the smaller particles of the sorbents. Pine bark and almond shell pretreated with formaldehyde presented higher sorption efficiency (95%), followed by almond shell (87%) and pine bark (82%) washed with hot water. All the sorption isotherms were found to fit a Freundlich equation, with correlation coefficients (R ²) between 0.823 and 0.989. The sorption coefficient (K _F) ranged from 0.06 to 0.74 (mg^1?1/n ·L ^1/n ·g ^?1). These results indicate that utilisation of both materials as an alternative sorbent for the removal of bisphenol A from contaminated waters is promising because they are available in large amounts and have an acceptable cost–efficiency ratio when compared with traditional adsorbents.     

管网生物膜菌株胞外聚合物的提取方法比较

以饮用水管网生物膜样品中一株强成膜能力的菌株Pleomorphomonas oryzae作为研究对象,考察了8种方法(高速离心法、超声法、加热法、EDTA法、H2SO4法、NaOH法、SDS法、甲醛法)对菌株胞外聚合物(EPS)的提取效果,并结合三维荧光光谱(EEM)和傅立叶红外光谱(FTIR)对提取的EPS进行成分分析.结果表明,EDTA法和H2SO4法既能提高EPS的提取效率,提取量分别为64.77 mg.g-1SS和74.43 mg.g-1SS,是离心方法提取量的1.62倍和1.86倍,又不会在提取过程中对菌株细胞造成破坏,是较为理想的EPS提取方法.EEM分析进一步证实,NaOH法对菌株细胞破坏严重,造成EPS成分变化较大.FTIR分析则说明,化学提取方法相较于物理提取方法会引入杂质对组分测定造成干扰.     

Sulfamethoxazole removal from polluted water by immobilized photocatalysis

The photocatalytic activity of TiO₂ deposits (Degussa P25 and Millennium PC500) has been studied using sulfamethoxazole (SMX) as a model water pollutant and a UV fluorescent lamp as a light source (365 nm). Both catalysts have shown very similar properties in the photocatalytic degradation of SMX. Special attention has been given to the effect of the irradiation time, pH, and pollutant concentration. No mass-transfer limitations are observed. The degradation of SMX is accelerated at low concentration, and the photocatalytic degradation kinetics obey the Langmuir–Hinshelwood model, allowing the adsorption and apparent rate constants to be determined for both catalysts.     

Heterogeneous photocatalysis for removal of microbes from water

Increasing water pollution by microbes has become a source of serious health concern across the globe. Production of potentially carcinogenic disinfection by-products has marred credibility of traditional water purification techniques like chlorination. Photocatalysis has emerged as a promising alternative technique for the disinfection of water with minimal risk of harmful by-products. The process involves a wide band gap semiconductor material which, upon irradiation of light, produces electrons and holes with high redox potential to degrade organic contaminants and microbes. In this review, we analyze the research trends in photocatalytic inactivation of water borne microorganisms. This report analyzes the major factors that affect the disinfection efficiency using this process. The discussion also includes plausible mechanisms of microbial degradation as well as a kinetic model of the inactivation process. Different approaches, like doping of semiconductors or energy band engineering or plasmon coupling, have been reported for the enhancement and utilization of ambient solar light. Photocatalysis could be a cost-effective and environmentally friendly water purification technique though further research is required to enhance its efficiency with the use of solar light.