Eilhann E. Kwon

Occurrences and removal of pharmaceuticals and personal care products (PPCPs) in drinking water and water/sewage treatment plants: A review

In recent years, many of micropollutants have been widely detected because of continuous input of pharmaceuticals and personal care products (PPCPs) into the environment and newly developed state-of-the-art analytical methods. PPCP residues are frequently detected in drinking water sources, sewage treatment plants (STPs), and water treatment plants (WTPs) due to their universal consumption, low human metabolic capability, and improper disposal. When partially metabolized PPCPs are transferred into STPs, they elicit negative effects on biological treatment processes; therefore, conventional STPs are insufficient when it comes to PPCP removal. Furthermore, the excreted metabolites may become secondary pollutants and can be further modified in receiving water bodies. Several advanced treatment systems, including membrane filtration, granular activated carbon, and advanced oxidation processes, have been used for the effective removal of individual PPCPs. This review covers the occurrence patterns of PPCPs in water environments and the techniques adopted for their treatment in STP/WTP unit processes operating in various countries. The aim of this review is to provide a comprehensive summary of the removal and fate of PPCPs in different treatment facilities as well as the optimum methods for their elimination in STP and WTP systems.

Sequential co-production of biodiesel and bioethanol with spent coffee grounds.

The sequential co-production of bioethanol and biodiesel from spent coffee grounds was investigated. The direct conversion of bioethanol from spent coffee grounds was not found to be a desirable option because of the relatively slow enzymatic saccharification behavior in the presence of triglycerides and the free fatty acids (FFAs) found to exist in the raw materials. Similarly, the direct transformation of the spent coffee grounds into ethanol without first extracting lipids was not found to be a feasible alternative. However, the crude lipids extracted from the spent coffee grounds were themselves converted into fatty acid methyl ester (FAME) and fatty acid ethyl ester (FAEE) via the non-catalytic biodiesel transesterification reaction. The yields of bioethanol and biodiesel were 0.46 g g(-1) and 97.5±0.5%, which were calculated based on consumed sugar and lipids extracted from spent coffee grounds respectively. Thus, this study clearly validated our theory that spent coffee grounds could be a strong candidate for the production of bioethanol and biodiesel.

Recent advances in photocatalytic treatment of pollutants in aqueous media

Photocatalysis can be an excellent solution for resolving the worlds energy and environmental problems. It has a wide range of applications for the decontamination of diverse hazardous pollutants in aqueous media. Technological progress in this research field has been achieved toward the improvement of the solar sensitivity to enhance the efficiency of pollutant decontamination. As a result, various strategies have been introduced to upgrade photocatalytic performance with the modification of prototypical photocatalyst such as doping, dye sensitization, semiconductor coupling, mesoporous supports, single site, and nano-based catalysts. In this review, a brief survey is presented to describe those strategies based on the evaluation made against various pollutants (such as pharmaceuticals, pesticides, heavy metals, detergents, and dyes) in aqueous media.

Biodiesel Production from Sewage Sludge: New Paradigm for Mining Energy from Municipal Hazardous Material

This work demonstrates that the production of biodiesel using the lipids extracted from sewage sludge (SS) could be economically feasible because of the remarkably high yield of oil and low cost of this feedstock, as compared to conventional biodiesel feedstocks. The yield of oil from SS, 980,000 L ha(-1) year(-1), is superior to those from microalgal and soybean oils, 446 and 2200 L ha(-1) year(-1), respectively. According to the case study of South Korea, the price of the lipids extracted from SS was approximately

Effect of carbon dioxide on the thermal degradation of lignocellulosic biomass.

0.03 L(-1) (USD), which is lower than those of all current biodiesel feedstocks. This work also highlights the insight of a novel methodology for transforming lipids containing high amounts of free fatty acids (FFAs) to biodiesel using a thermochemical process under ambient pressure in a continuous flow system. This allowed the combination of esterification of FFAs and transesterification of triglycerides into a single noncatalytic process, which led to a 98.5% ± 0.5% conversion efficiency to FAME (fatty acid methyl ester) within 1 min in a temperature range of 350-500 °C. The new process for converting the lipids extracted from SS shows high potential to achieve a major breakthrough in minimizing the cost of biodiesel production owing to its simplicity and technical advantages, as well as environmental benefits.

Transfer of antibiotic resistance plasmids in pure and activated sludge cultures in the presence of environmentally representative micro-contaminant concentrations

Using biomass as a renewable energy source via currently available thermochemical processes (i.e., pyrolysis and gasification) is environmentally advantageous owing to its intrinsic carbon neutrality. Developing methodologies to enhance the thermal efficiency of these proven technologies is therefore imperative. This study aimed to investigate the use of CO2 as a reaction medium to increase not only thermal efficiency but also environmental benefit. The influence of CO2 on thermochemical processes at a fundamental level was experimentally validated with the main constituents of biomass (i.e., cellulose and xylan) to avoid complexities arising from the heterogeneous matrix of biomass. For instance, gaseous products including H2, CH4, and CO were substantially enhanced in the presence of CO2 because CO2 expedited thermal cracking behavior (i.e., 200-1000%). This behavior was then universally observed in our case study with real biomass (i.e., corn stover) during pyrolysis and steam gasification. However, further study is urgently needed to optimize these experimental findings.

Metal–organic frameworks for the control and management of air quality: advances and future direction

The presence of antibiotics in the natural environment has been a growing issue. This presence could also account for the influence that affects microorganisms in such a way that they develop resistance against these antibiotics. The aim of this study was to evaluate whether the antibiotic resistant gene (ARG) plasmid transfer can be facilitated by the impact of 1) environmentally representative micro-contaminant concentrations in ppb (part per billion) levels and 2) donor-recipient microbial complexity (pure vs. mixed). For this purpose, the multidrug resistant plasmid, pB10, and Escherichia coli DH5α were used as a model plasmid and a model donor, respectively. Based on conjugation experiments with pure (Pseudomonas aeruginosa PAKexoT) and mixed (activated sludge) cultures as recipients, increased relative plasmid transfer frequencies were observed at ppb (μg/L) levels of tetracycline and sulfamethoxazole micro-contaminant exposure. When sludge, a more complex community, was used as a recipient, the increases of the plasmid transfer rate were always statistically significant but not always in P. aeruginosa. The low concentration (10 ppb) of tetracycline exposure led to the pB10 transfer to enteric bacteria, which are clinically important pathogens.

Carbon dioxide assisted sustainability enhancement of pyrolysis of waste biomass: A case study with spent coffee ground.

Recently, the potential role of metal–organic framework (MOFs) and porous coordination polymers (PCPs) has been recognized in the field of air quality management (AQM) due to their intrinsically tunable chemical structure and multifunctional properties which afforded significant enhancements in adsorption capacities, catalytic degradation, and removal of diverse airborne pollutants and other vapors. A diverse range of MOFs was investigated for separation, capture, and storage of greenhouse gases and other pollutants (including volatile organic compounds (VOCs), sulfur compounds, and chemical warfare agents (CWAs)). It should however be noted that some drawbacks of MOFs are also found such as: poor selectivity, high energy and fiscal cost, low capacity, and difficulties in regeneration. Here, we provide an up-to-date review on the promising role of MOFs in the field of AQM in relation to the diverse available synthesis methods. As such, we hope to provide future directions such that MOFs/PCPs can make a bright contribution to air quality control.

Utilizing Carbon Dioxide as a Reaction Medium to Mitigate Production of Polycyclic Aromatic Hydrocarbons from the Thermal Decomposition of Styrene Butadiene Rubber

This work mainly presents the influence of CO2 as a reaction medium in the thermo-chemical process (pyrolysis) of waste biomass. Our experimental work mechanistically validated two key roles of CO2 in pyrolysis of biomass. For example, CO2 expedited the thermal cracking of volatile organic compounds (VOCs) evolved from the thermal degradation of spent coffee ground (SCG) and reacted with VOCs. This enhanced thermal cracking behavior and reaction triggered by CO2 directly led to the enhanced generation of CO (∼ 3000%) in the presence of CO2. As a result, this identified influence of CO2 also directly led to the substantial decrease (∼ 40-60%) of the condensable hydrocarbons (tar). Finally, the morphologic change of biochar was distinctive in the presence of CO2. Therefore, a series of the adsorption experiments with dye were conducted to preliminary explore the physico-chemical properties of biochar induced by CO2.

Transforming animal fats into biodiesel using charcoal and CO2.

The CO(2) cofeed impact on the pyrolysis of styrene butadiene rubber (SBR) was investigated using thermogravimetric analysis (TGA) coupled to online gas chromatography/mass spectroscopy (GC/MS). The direct comparison of the chemical species evolved from the thermal degradation of SBR in N(2) and CO(2) led to a preliminary mechanistic understanding of the formation and relationship of light hydrocarbons (C(1-4)), aromatic derivatives, and polycyclic aromatic hydrocarbons (PAHs), clarifying the role of CO(2) in the thermal degradation of SBR. The identification and quantification of over 50 major and minor chemical species from hydrogen and benzo[ghi]perylene were carried out experimentally in the temperature regime between 300 and 500 °C in N(2) and CO(2). The significant amounts of benzene derivatives from the direct bond dissociation of the backbone of SBR, induced by thermal degradation, provided favorable conditions for PAHs by the gas-phase addition reaction at a relatively low temperature compared to that with conventional fuels such as coal and petroleum-derived fuels. However, the formation of PAHs in a CO(2) atmosphere was decreased considerably (i.e., ∼50%) by the enhanced thermal cracking behavior, and the ultimate fates of these species were determined by different pathways in CO(2) and N(2) atmospheres. Consequently, this work has provided a new approach to mitigate PAHs by utilizing CO(2) as a reaction medium in thermochemical processes.