Cheng-Fang Lin

Pharmaceutical contamination in residential, industrial, and agricultural waste streams: risk to aqueous environments in Taiwan.

This is a comprehensive study of the occurrence of antibiotics, hormones and other pharmaceuticals in water sites that have major potential for downstream environmental contamination. These include residential (hospitals, sewage treatment plants, and regional discharges), industrial (pharmaceutical production facilities), and agricultural (animal husbandries and aquacultures) waste streams. We assayed 23 Taiwanese water sites for 97 targeted compounds, of which a significant number were detected and quantified. The most frequently detected compounds were sulfamethoxazole, caffeine, acetaminophen, and ibuprofen, followed closely by cephalexin, ofloxacin, and diclofenac, which were detected in >91% of samples and found to have median (maximum) concentrations of 0.2 (5.8), 0.39 (24.0), 0.02 (100.4), 0.41 (14.5), 0.15 (31.4), 0.14 (13.6) and 0.083 (29.8) microg/L, respectively. Lincomycin and acetaminophen had high measured concentrations (>100 microg/L), and 35 other pharmaceuticals occurred at the microg/L level. These incidence and concentration results correlate well with published data for other worldwide locations, as well as with Taiwanese medication usage data, suggesting a human contamination source. Many pharmaceuticals also occurred at levels exceeding predicted no-effect concentrations (PNEC), warranting further investigation of their occurrence and fate in receiving waters, as well as the overall risks they pose for local ecosystems and human residents. The information provided here will also be useful for development of strategies for regulation and remediation.

Characterization of arsenate adsorption on hydrous iron oxide using chemical and physical methods

Abstract The adsorption of arsenate by hydrous iron oxide was investigated by both chemical and physical energy dispersive analysis of X-rays (EDAX) and Fourier transform infrared (FTIR) methods. The chemical methods for characterizing arsenate adsorption sites on hydrous iron oxide surfaces in this work were investigations of the effect of ionic strength and zeta potential measurements of iron oxide systems containing various arsenate concentrations over the pH range 4–10. An inner-sphere complexation at the aqueous arsenate/iron oxide interface was identified from the results of the ionic strength effect and the shift in isoelectric point of the system. Evidence for direct coordination of arsenate to the surface of iron oxide was obtained by EDAX and FTIR techniques. Results from these physical methods showed that arsenate was chemisorbed on the iron oxide surface. Specific adsorption could therefore be deduced, on the basis of both chemical and physical methods, to occur at the aqueous arsenate and solid iron oxide interfaces.

Total recovery of resources and energy from rice straw using microwave-induced pyrolysis

This article presents the application of microwave-induced pyrolysis to total recovery of resources and energy from rice straw. The microwave power and particle size of feedstock were both key parameters affecting the performance of microwave-induced pyrolysis. Under 400-500W microwave power, the reduction of fixed carbon in the biomass was significant. From the experimental results of specific surface area, zeta potential, and Cu2+ adsorption, the applications of solid residues in the water and wastewater treatment could be expected. The major compositions in gaseous product were H2, CO2, CO, CH4 of 55, 17, 13, 10vol.%, respectively. The high H2 content might imply that microwave-induced pyrolysis of biomass waste has the potential to produce the H2-rich fuel gas. Alkanes, polars, and low-ringed polycyclic aromatic hydrocarbons were three primary kinds of compounds in the liquid product.

Hydrogen-rich fuel gas from rice straw via microwave-induced pyrolysis

This study aimed to research the productivity of H(2)-rich fuel gas from rice straw using the microwave-induced pyrolysis. The formation constituents of gas product and the mechanism of its production were also discussed. The primary components of gas product were H(2), CO(2), CO, and CH(4), with average percentages of 50.67, 22.56, 16.09, and 7.42vol.%, respectively. According to the TA-MS analysis, it was suggested that focused heating by microwaves made the microwave-induced pyrolysis different from the traditional pyrolysis. A chemical equation could be nearly balanced to illustrate the gas composition generated from rice straw. From the viewpoint of energy consumption, close to 60% of the input energy could be derived and utilized as bioenergy.

Sorption and biodegradation of sulfonamide antibiotics by activated sludge: Experimental assessment using batch data obtained under aerobic conditions

This study investigated the adsorption, desorption, and biodegradation characteristics of sulfonamide antibiotics in the presence of activated sludge with and without being subjected to NaN(3) biocide. Batch experiments were conducted and the relative contributions of adsorption and biodegradation to the observed removal of sulfonamide antibiotics were determined. Three sulfonamide antibiotics including sulfamethoxazole (SMX), sulfadimethoxine (SDM), and sulfamonomethoxine (SMM), which had been detected in the influent and the activated sludge of wastewater treatment plants (WWTP) in Taiwan, were selected for this study. Experimental results showed that the antibiotic compounds were removed via sorption and biodegradation by the activated sludge, though biodegradation was inhibited in the first 12 h possibly due to competitive inhibition of xenobiotic oxidation by readily biodegradable substances. The affinity of sulfonamides to sterilized sludge was in the order of SDM > SMM > SMX. The sulfonamides existed predominantly as anions at the study pH of 6.8, which resulted in a low level of adsorption to the activated sludge. The adsorption/desorption isotherms were of a linear form, as well described by the Freundlich isotherm with the n value approximating unity. The linear distribution coefficients (K(d)) were determined from batch equilibrium experiments with values of 28.6 ± 1.9, 55.7 ± 2.2, and 110.0 ± 4.6 mL/g for SMX, SMM, and SDM, respectively. SMX, SMM, and SDM desorb reversibly from the activated sludge leaving behind on the solids 0.9%, 1.6%, and 5.2% of the original sorption dose of 100 μg/L. The sorbed antibiotics can be introduced into the environment if no further treatments were employed to remove them from the biomass.

Effect of functional groups of humic substances on uf performance

The role of different functional groups present in humic substances on the membrane flux is unclear. This study is undertaken to (1) separate the carboxyl and phenolic groups from a humic solution, and (2) evaluate the effect of each fractionated humic substances on the ultrafiltration (UF) performance. A weak-base amine resin was used for the adsorption (pH 7) and the subsequent desorption (pH 13) of the phenolic groups from a commercial humic solution. These fractions were evaluated qualitatively (via Fourier transform infrared spectroscopy) and quantitatively (titration); they were further subjected to the analyses of the trihalomethane formation potential (THMFP) and ultrafiltration performance. Although, a complete separation of the phenolic and carboxyl groups is not possible, the results nevertheless provide useful information about their effects on UF performance. The fraction with a higher content of the phenolic OH group exhibits the highest THMFP (190 microg/mg C), whereas the fraction with a higher content of the carboxyl groups exhibits more flux decline. The UF system evaluated is unable to remove a significant portion of THM precursors, resulting in high THMs in permeate. The use of powdered activated carbon for the pretreatment of these fractions fails to improve membrane fouling. The pore size of UF membrane does not appear to affect the membrane flux, and the switch from the hydrophobic to hydrophilic membrane only slight improves the permeate flux.

Competitive adsorption of molybdate, chromate, sulfate, selenate, and selenite on γ-Al2O3

Competitive adsorption of molybdate, selenite, selenate, chromate, and sulfate onto γ-Al2O3 was investigated in the present study. Binary-solute systems of MoO42−/SeO32−, CrO42−/SO42−, and CrO42−/SeO42− as well as single anion systems were evaluated for the relative influence on competitive adsorption on oxide surface. As would be expected, the adsorption density of each anion in the binary-solute systems decreases, as compared to the respective density in a single anion system. Furthermore, MoO42− inhibits SeO32− adsorption in acidic condition and that SO42− or SeO42− depresses CrO42−. The order of the relative retainment of anions on oxide surface is molybdate>selenite>selenate∼sulfate>chromate, which corresponds to the magnitude of the overall proton coefficient of the corresponding anions.

Stabilization of cadmium contaminated soils using synthesized zeolite

Abstract This research investigates the effect of synthesized zeolite on stabilizing Cd-contaminated soil, using 0.01 M CaCl2 leaching solution in batch and column experiments. The zeolite was synthesized from fly ash obtained from a Coal-Fired Power Plant, by adding 2 N NaOH and subjecting to 90°C for 24 h. The experiment used two groups of soil samples: (1) addition of Cd to four series of background soils: Pinchen, Jente, Erlin and Chengchung; (2) actual contaminated soils from Chungsing and Tsasta sites. The result of the batch experiment indicates that the addition of zeolite reduces Cd leaching from all types of contaminated soils. The more zeolite added, the lower Cd concentrations were detected in the leaching solution. The stabilized Cd in soils in the presence of zeolite is also demonstrated in the column experiments; the leachate contains insignificant Cd, and Cd depth analysis of the soil columns shows little Cd migration. For example, for Pinchen and Jente soils, after 12 and 49 pore volumes of leaching solution, the remaining Cd levels in the soils were 12% and 35%, respectively, of the original Cd values with no zeolite added, as compared to 96% and 99% in the presence of 16% zeolite. The higher cation exchange capacity of the zeolite/soil mixtures and higher pH are responsible for stabilizing Cd in soils. The effect is most useful in application to the acidic sandy soils to prevent contaminated heavy metals from leaching.

Greenhouse gases emissions from waste management practices using Life Cycle Inventory model

When exploring the correlation between municipal solid waste management and green house gas emission, the volume and physical composition of the waste matter must be taken into account. Due to differences in local environments and lifestyles the quantity and composition of waste often vary. This leads to differences in waste treatment methods and causes different volumes of greenhouse gases (GHGs), highlighting the need for local research. In this study the Life Cycle Inventory method was used with global warming indicator GHGs as the variables. By quantifying the data and adopting a region-based approach, this created a model of household MSWM in Taipei City, a metropolitan region in Taiwan. To allow analysis and comparison a compensatory system was then added to expand the system boundary. The results of the analysis indicated that out of all the solid waste management sub-models for a function unit, recycling was the most effective method for reducing GHG emissions while using kitchen food waste as swine feeding resulted in the most GHG emissions. As for the impact of waste collection vehicles on emissions, if the efficiency of transportation could be improved and energy consumption reduced, this will help solid waste management to achieve its goal of reducing GHG emissions.

Fate of sulfonamide antibiotics in contact with activated sludge – Sorption and biodegradation

The sorption and biodegradation of three sulfonamide antibiotics, namely sulfamethoxazole (SMX), sulfadimethoxine (SDM), and sulfamonomethoxine (SMM), in an activated sludge system were investigated. Experiments were carried out by contacting 100 μg/L of each sulfonamide compound individually with 2.56 g/L of MLSS at 25±0.5 °C, pH 7.0, and dissolved oxygen of 3.0±0.1 mg/L in a batch reactor over different periods of 2 d and 14 d. All sulfonamides were removed completely over 11-13 d. Sorptive equilibrium was established well within the first few hours, followed by a lag period of 1-3 days before biodegradation was to deplete the antibiotic compounds linearly in the ensuing 10 days. Apparent zeroth-order rate constants were obtained by regression analysis of measured aqueous concentration vs. time profiles to a kinetic model accounting for sorption and biodegradation; they were 8.1, 7.9, and 7.7 μg/L/d for SDM, SMX, and SMM, respectively, at activated sludge concentration of 2.56 g/L. The measured kinetics implied that with typical hydraulic retention time (e.g. 6 h) provided by WWTP the removal of sulfonamide compounds from the wastewater during the activated sludge process would approximate 2 μg/L.