Estimation of nitrous oxide emissions from rice paddy fields using the DNDC model: a case study of South Korea.

The Denitrification-Decomposition (DNDC)-Rice is a mechanistic model which is widely used for the simulation and estimation of greenhouse gas emissions [nitrous oxide (N2O)] from soils under rice cultivation. N2O emissions from paddy fields in South Korea are of high importance for their cumulative effect on climate. The objective of this study was to estimate the N2O emissions and biogeochemical factors involved in N2O emissions such as ammonium (NH4+) and nitrate (NO3-) using the DNDC model in the rice-growing regions of South Korea. N2O emission was observed at every application of fertilizer and during end-season drainage at different rice-growing regions in South Korea. Maximum NH4+ and NO3- were observed at 0-10 cm depth of soil. NH4+ increased at each fertilizer application and no change in NO3- was observed during flooding. NH4+ decreased and NO3- increased simultaneously at end-season drainage. Minimum and maximum cumulative N2O emissions were observed at Chungcheongbuk-do and Jeju-do regions of South Korea, respectively. The simulated average cumulative N2O emission in rice paddies of South Korea was 1.37 kg N2O-N ha-1 season-1. This study will help in calculating the total nitrogen emissions from agriculture land of South Korea and the World.

A figure of merits-based performance comparison of various advanced functional nanomaterials for adsorptive removal of gaseous ammonia.

The implementation of sustainable industrial development based on energy/cost-effective techniques with zero/low rate of pollutant emission is an ideal strategy for the proper management of a natural environment. Gaseous ammonia released from a variety of anthropogenic sources (e.g., agriculture, pharmaceuticals, commercial cleaning products, and refrigerant) is estimated to be as high as 150 million tons∙year-1. To reduce the negative effects of atmospheric ammonia, the great utility of advanced functional nanomaterials (e.g., metal organic frameworks, covalent organic polymers, metal/metal oxide nanoparticles, and carbon nanostructures) has been recognized. To gain a better understanding of the sorptive removal potential of diverse materials, their performance has been evaluated based on the key performance merits (e.g., initial concentration, sorption capacity, and partition coefficient). Generally, the PC values can be applied to significantly estimate the contaminant adsorption potential of NMs via balancing the biased influences of operating parameters (e.g., initial concentration of pollutants) as perceived for the partitioning of compounds between aqueous phases at equilibrium (e.g., Henry's Law). Therefore, in this work, we have proposed the PC as a prosperous performance merit (in terms of heterogeneity of surface and strength of adsorption process) for the selection of high performance nano-adsorbents for gaseous ammonia. Moreover, the water stability, recyclability, economic aspects, and future perspectives have also been discussed for real-world applications of advanced nanomaterial against gaseous ammonia adsorption. The outcome of this evaluation will be expedient for the classification/selection of the most effectual and cost-effective options for mitigation of environmental pollutants like gaseous ammonia.

Metal oxide and carbon nanomaterial based membranes for reverse osmosis and membrane distillation: A comparative review.

Commercial membranes typically suffer from fouling and wetting during membrane distillation (MD). In contrast, reverse osmosis (RO) can be subject to the fouling issue if applied for highly saline feed solutions containing foulants (e.g., organics, oils, and surfactants). Among the diverse treatment options, the nanomaterial-based membranes have recently gained great interest due to their advantageous properties (e.g., enhanced flux and roughness, better pore size distribution, and higher conductivity). This review focuses on recent advances in the mechanical properties, anti-fouling capabilities, salt rejection, and economic viability of metal oxide (SiO2, TiO2, and ZnO) and carbon nanomaterial (graphene oxide/carbon nanotube)-based membranes. Current challenges in applying nanomaterial-based membranes are also discussed. The study further describes the preparation methods, mechanisms, commercial applications, and economical feasibility of metal oxide- and carbon nanomaterial-based membrane technologies.

Nanotechnology-based sorption and membrane technologies for the treatment of petroleum-based pollutants in natural ecosystems and wastewater streams.

Petroleum processing wastewater (PPW) is a complex mixture of free, soluble, and emulsive hydrocarbons that often contain heavy metals and/or solid particles. As these hazardous constituents can accumulate in human beings and the environment, exposure to the PPW can have harmful effects in various respects. The use of environmental nanotechnologies (E-Nano) is considered an attractive option to resolve the problems associated with PPW. Among different treatment technologies, E-Nano-based sorption (adsorption/absorption) and membrane filtration approaches have been proven to have outstanding efficacy in remediation of PPW pollutants. It is, however, crucial to determine the appropriate technological option (e.g., low-cost operational conditions) for the practical application of such technologies. In this review, the potential of E-Nano-based sorption and membrane technologies in the treatment of various PPW pollutants is discussed based on their performances in comparison to traditional technologies. Their suitability is evaluated further in relation to their merits/disadvantages and economic feasibility with the goal of constructing a perspective map to efficiently implement the E-Nano technologies.

Utilization of activated carbon as an effective replacement for a commercialized three-bed sorbent (Carbopack) to quantitate aromatic hydrocarbons in ambient air.

The potential use of activated carbon (AC) as an inexpensive and effective alternative sorbent material in thermal desorption is presented and validated for the analysis of aromatic volatile organic compounds (VOCs) such as benzene, toluene, m-xylene, and styrene (BTXS) in air. The optimum desorption conditions of an AC sampling tube (2 mg AC bed) were determined and compared with a commercial three-bed (Carbopack; C + B + X) tube sampler as a reference. The AC sampler exhibited good linearity (R2 > 0.99) and reproducibility (RSE of 2.38 ±â€¯0.21%) for BTXS analysis. The AC tube sampler showed good storability (up to 3 d) and excellent recyclability (up to 50 cycles). An analysis of BTXS in ambient air showed excellent agreement between AC and CBX (bias < 5%). The 1% breakthrough volume values for 2 mg AC, when tested at 100 ppb of benzene as a sole component or in a BTXS mixture, were 10,000 or 5000 L g-1, respectively. The results of this study support the performance of AC as a suitable medium for sampling VOCs as reliable as high-cost commercial sorbent products.

Nanomaterials-based treatment options for chromium in aqueous environments.

Sustainable development and the restoration of ecosystems are the important goals for civilization. Currently, heavy metal contamination of aquatic environments has become a serious issue. Chromium (Cr) is simultaneously an essential metallic element and one of 20 chemicals posing a maximum threat to living beings. To mitigate that threat, various treatment methods have been developed, including adsorption, electrocoagulation, photoelectrocatalysis, fuel cells, bioremediation, chemical precipitation, ultrafiltration, ion exchange, and co-precipitation. However, selection of the most energy- and cost-efficient wastewater treatment option has proven challenging, as each approach is subject to shortcomings involving energy consumption, treatment capacity, and efficiency. This review describes the potential role of diverse functional nanomaterials (e.g., iron/iron oxide nanoparticles, carbon nanostructures, metal organic frameworks, and their commercial counterparts) in treatment of Cr in aqueous environments with respect to key figure of merits, such as, adsorption capacity, removal efficiency, and partition coefficient. In addition, their performance was compared with the most common treatment options. The results of this study will help determine the most effective and economical options for control of Cr in aquatic environments.

Competitive adsorption of gaseous aromatic hydrocarbons in a binary mixture on nanoporous covalent organic polymers at various partial pressures.

Covalent-organic polymers (COPs) are recognized for their great potential for treating diverse pollutants via adsorption. In this study, the sorption behavior of benzene and toluene was investigated both individually and in a binary mixture against two types of COPs possessing different -NH2 functionalities. Namely, the potential of COPs was tested against benzene and toluene in a low inlet partial pressure range (0.5-20 Pa) using carbonyl-incorporated aromatic polymer (CBAP)-1-based diethylenediamine (EDA) [CD] and ethylenetriamine (DETA) [CE]. The maximum adsorption capacity and breakthrough values of both COPs showed dynamic changes with increases in the partial pressures of benzene and toluene. The maximum adsorption capacities (Amax) of benzene (as the sole component in N2 under atmospheric conditions) on CD and CE were in the range of 24-36 and 33-75 mg g-1, respectively. In contrast, with benzene and toluene in a binary mixture, the benzene Amax decreased more than two-fold (range of 2.7-15 and 6-39 mg g-1, respectively) due to competition with toluene for sorption sites. In contrast, the toluene Amax values remained consistent, reflecting its competitive dominance over benzene. The adsorption behavior of the targeted compounds (i.e., benzene and toluene) was explained by fitting the adsorption data by diverse isotherm models (e.g., Langmuir, Freundlich, Elovich, and Dubinin-Radushkevich). The current research would be helpful for acquiring a better understanding of the factors affecting competitive adsorption between different VOCs in relation to a given sorbent and across varying partial pressures.

Treatment of synthetic arsenate wastewater with iron-air fuel cell electrocoagulation to supply drinking water and electricity in remote areas.

Electrocoagulation with an iron-air fuel cell is an innovative arsenate removal system that can operate without an external electricity supply. Thus, this technology is advantageous for treating wastewater in remote regions where it is difficult to supply electricity. In this study, the possibility of real applications of this system for arsenate treatment with electricity production was verified through electrolyte effect investigations using a small-scale fuel cell and performance testing of a liter-scale fuel cell stack. The electrolyte species studied were NaCl, Na2SO4, and NaHCO3. NaCl was overall the most effective electrolyte for arsenate treatment, although Na2SO4 produced the greatest electrical current and power density. In addition, although the current density and power density were proportional to the concentrations of NaCl and Na2SO4, the use of concentrations above 20 mM of NaCl and Na2SO4 inhibited arsenate treatment due to competition effects between anions and arsenate in adsorption onto the iron hydroxide. The dominant iron hydroxide produced at the iron anode was found to be lepidocrocite by means of Raman spectroscopy. A liter-scale four-stack iron-air fuel cell with 10 mM NaCl electrolyte was found to be able to treat about 300 L of 1 ppm arsenate solution to below 10 ppb during 1 day, based on its 60-min treatment capacity, as well as produce the maximum power density of 250 mW/m2.

Arsenic treatment and power generation with a dual-chambered fuel cell with anionic and cationic membranes using NaHCO3 anolyte and HCl or NaCl catholyte.

Dual-chambered fuel cells with an iron anode and an air-carbon cathode separated by an ion exchange membranes have been used to treat arsenate during power production. To select an effective catholyte, the dual-chambered fuel cell consisted 90 mL of 0.1 M HCl or 0.5 M NaCl as the catholyte and 1 L of 0.1 M NaHCO3 as the anolyte at an initial pH 5. The 0.1 M HCl was an effective catholyte, with which 1 ppm arsenate in 1 L of anolyte was reduced to 5 ppb in 1 h, and the maximum power density was about 6.3 w/m2 with an anion exchange membrane fuel cell (AEM_FC) and 4.4 w/m2 with a cation exchange membrane fuel cell (CEM_FC). Therefore, 90 mL of 0.1 M HCl was used as a catholyte to treat 20 L of 0.1 M NaHCO3 anolyte containing 1 ppm arsenate at an initial pH of 5 or 7. The arsenate level at pH 5 decreased to less than 5 ppb in 4 h, and the maximum power density was 5.9 W/m2 and 4.7 W/m2 with AEM_FC and CEM_FC, respectively. When using 0.01 M NaHCO3 as the anolyte at pH 5, arsenate was reduced to less than 5 ppb in 8 and 24 h for AEC_FC and CEM_FC, respectively. However, when using an anolyte at pH 7, arsenate could not be effectively removed in 24 h. Therefore, when using carbonate as an anolyte, the solution should be adjusted to a weakly acidic pH in order to remove arsenate.

Scaled-up dual anode/cathode microbial fuel cell stack for actual ethanolamine wastewater treatment.

The aim of this work was to develop the scale-up microbial fuel cell technology for actual ethanolamine wastewater treatment, dual anode/cathode MFC stacks connected in series to achieve any desired current, treatment capacity, and volume capacity. However, after feeding actual wastewater into the MFC, maximum power density decreased while the corresponding internal resistance increased. With continuous electricity production, a stack of eight MFCs in series achieved 96.05% of COD removal and 97.30% of ammonia removal at a flow rate of 15.98L/d (HRT 12h). The scaled-up dual anode/cathode MFC stack system in this research was demonstrated to treat actual ETA wastewater with the added benefit of harvesting electricity energy.

The enhancement of ammonium removal from ethanolamine wastewater using air-cathode microbial fuel cells coupled to ferric reduction.

A microbial fuel cell (MFC) with biological Fe(III) reduction was implemented for simultaneous ethanolamine (ETA) degradation and electrical energy generation. In the feasibility experiment using acetate as a substrate in a single-chamber MFC with goethite and ammonium at a ratio of 3.0(mol/mol), up to 96.1% of the ammonium was removed through the novel process related to Fe(III). In addition, the highest voltage output (0.53V) and maximum power density (0.49Wm(-2)) were obtained. However, the ammonium removal and electrical performance decreased as acetate was replaced with ETA. In the long-term experiment, the electrical performance markedly decreased where the voltage loss increased due to Fe deposition on the membranes.