Walter Den

Bioadsorber efficiency, design, and performance forecasting for alachlor removal

This study discusses a mathematical modeling and design protocol for bioactive granular activated carbon (GAC) adsorbers employed for purification of drinking water contaminated by chlorinated pesticides, exemplified by alachlor. A thin biofilm model is discussed that incorporates the following phenomenological aspects: film transfer from the bulk fluid to the adsorbent particles, diffusion through the biofilm immobilized on adsorbent surface, adsorption of the contaminant into the adsorbent particle. The modeling approach involved independent laboratory-scale experiments to determine the model input parameters. These experiments included adsorption isotherm studies, adsorption rate studies, and biokinetic studies. Bioactive expanded-bed adsorber experiments were conducted to obtain realistic experimental data for determining the ability of the model for predicting adsorber dynamics under different operating conditions. The model equations were solved using a computationally efficient hybrid numerical technique combining orthogonal collocation and finite difference methods. The model provided accurate predictions of adsorber dynamics for bioactive and non-bioactive scenarios. Sensitivity analyses demonstrated the significance of various model parameters, and focussed on enhancement in certain key parameters to improve the overall process efficiency. Scale-up simulation studies for bioactive and non-bioactive adsorbers provided comparisons between their performances, and illustrated the advantages of bioregeneration for enhancing their effective service life spans. Isolation of microbial species revealed that fungal strains were more efficient than bacterial strains in metabolizing alachlor. Microbial degradation pathways for alachlor were proposed and confirmed by the detection of biotransformation metabolites and byproducts using gas chromatography/mass spectrometry.

Analysis of trace contamination of phthalate esters in ultrapure water using a modified solid-phase extraction procedure and automated thermal desorption-gas chromatography/mass spectrometry.

The present study was aimed to develop a procedure modified from the conventional solid-phase extraction (SPE) method for the analysis of trace concentration of phthalate esters in industrial ultrapure water (UPW). The proposed procedure allows UPW sample to be drawn through a sampling tube containing hydrophobic sorbent (Tenax TA) to concentrate the aqueous phthalate esters. The solid trap was then demoisturized by two-stage gas drying before subjecting to thermal desorption and analysis by gas chromatography-mass spectrometry. This process removes the solvent extraction procedure necessary for the conventional SPE method, and permits automation of the analytical procedure for high-volume analyses. Several important parameters, including desorption temperature and duration, packing quantity and demoisturizing procedure, were optimized in this study based on the analytical sensitivity for a standard mixture containing five different phthalate esters. The method detection limits for the five phthalate esters were between 36 ng l(-1) and 95 ng l(-1) and recovery rates between 15% and 101%. Dioctyl phthalate (DOP) was not recovered adequately because the compound was both poorly adsorbed and desorbed on and off Tenax TA sorbents. Furthermore, analyses of material leaching from poly(vinyl chloride) (PVC) tubes as well as the actual water samples showed that di-n-butyl phthalate (DBP) and di(2-ethylhexyl) phthalate (DEHP) were the common contaminants detected from PVC contaminated UPW and the actual UPW, as well as in tap water. The reduction of DEHP in the production processes of actual UPW was clearly observed, however a DEHP concentration of 0.20 microg l(-1) at the point of use was still being quantified, suggesting that the contamination of phthalate esters could present a barrier to the future cleanliness requirement of UPW. The work demonstrated that the proposed modified SPE procedure provided an effective method for rapid analysis and contamination identification in UPW production lines.

Organic Airborne Molecular Contamination in Semiconductor Fabrication Clean Rooms A Review

Monitoring of airborne molecular contamination (AMC) has become a crucial element of cleanroom management as the production phase of semiconductor devices marches deep into sub-100-nm range. The current understandings of the AMC, particularly those with organic origins, are presented comprehensively in this article based on the research reports within the past ten years. Starting with a review of the chronological development of AMC problems and several approaches for the AMC classifications, this article also examines the merits of several available ambient sampling and surface analytical methods. The focal point of the article is to address the surface deposition potential of organic AMCs by experimentally correlating the surface speciation and abundance of the organic AMCs with their physical and chemical characteristics, together with the kinetic models delineating the rates of deposition for both single-and multiple-contaminant scenarios. In addition, the current progress of the AMC control strategies, especially the development of the chemical filtration technology, is also examined in the paper.

Construction and Application of an Intelligent Air Quality Monitoring System for Healthcare Environment

Indoor air quality monitoring in healthcare environment has become a critical part of hospital management and policy. Manual air sampling and analysis are cost-inhibitive and do not provide real-time air quality data and response measures. In this month-long study over 14 sampling locations in a public hospital in Taiwan, we observed a positive correlation between CO2 concentration and population, total bacteria, and particulate matter concentrations, thus monitoring CO2 concentration as a general indicator for air quality could be a viable option. Consequently, an intelligent environmental monitoring system consisting of a CO2/temperature/humidity sensor, a digital plug, and a ZigBee Router and Coordinator was developed and tested. The system also included a backend server that received and analyzed data, as well as activating ventilation and air purifiers when CO2 concentration exceeded a pre-set value. Alert messages can also be delivered to offsite users through mobile devices.

Application of a multiwalled carbon nanotube-chitosan composite as an electrode in the electrosorption process for water purification

In this study, a multiwalled carbon nanotubes-chitosan (CNTs-CS) composite electrode was fabricated to enable water purification by electrosorption. The CNTs-CS composite electrode was shown to possess excellent capacitive behaviors and good pore accessibility by electrochemical impedance spectroscopy, galvanostatic charge-discharge, and cyclic voltammetry measurements in 1 M H2SO4 electrolyte. Moreover, the CNTs-CS composite electrode showed promising performance for capacitive water desalination. At an electric potential of 1.2 V, the electrosorption capacity and electrosorption rate of NaCl ions on the CNTs-CS composite electrode were determined to be 10.7 mg g(-1) and 0.051 min(-1), respectively, which were considerably higher than those of conventional activated electrodes. The improved electrosorption performance could be ascribed to the existence of mesopores. Additionally, the feasibility of electrosorptive removal of aniline from an aqueous solution has been demonstrated. Upon polarization at 0.6 V, the CNTs-CS composite electrode had a larger electrosorption capacity of 26.4 mg g(-1) and a higher electrosorption rate of 0.006 min(-1) for aniline compared with the open circuit condition. The enhanced adsorption resulted from the improved affinity between aniline and the electrode under electrochemical assistance involving a nonfaradic process. Consequently, the CNT-CS composite electrode, exhibiting typical double-layer capacitor behavior and a sufficient potential range, can be a potential electrode material for application in the electrosorption process.

Treatment of organic wastewater discharged from semiconductor manufacturing process by ultraviolet/hydrogen peroxide and biodegradation

This study investigates the feasibility of using a two-stage process combining a photochemical oxidation process (UV/H/sub 2/O/sub 2/) and a biological fluidized-bed system to treat dilate-organic wastewater discharged from semiconductor manufacturing facilities. This combined process has the merits of decomposing recalcitrant organic chemicals into intermediate products more amenable to biodegradation, thereby achieving high degree of mineralization of organic compounds that are otherwise toxic to aerobic biodegradation. Six organic solvents, including propylene glycol methyl ether acetate, ethyl lactate, tetramethylammonium hydroxide, 1-methyl-2-pyrrolidone, isopropanol, and phenol, were evaluated due to their common applications in various wafer fabrication processes. The optimal operating conditions (H/sub 2/O/sub 2/ dosage, pH, exposure time) for the first-stage UV/H/sub 2/O/sub 2/ were determined for each chemical, and a nominal condition was selected for the ensuing biodegradation, experiments. GC/MS analyses demonstrated that UV/H/sub 2/O/sub 2/ indeed decomposed the chemicals into smaller fragments that could be effectively mineralized by aerobic biodegradation.

Fouling characterization and control for harvesting microalgae Arthrospira (Spirulina) maxima using a submerged, disc-type ultrafiltration membrane.

This study characterized the fouling of a novel circular-disc ultrafiltration membrane in a submerged bioreactor system to harvest Arthrospira maxima cells. Flux-stepping study showed that the value of critical flux was below the smallest flux tested at 28.8lm(-2)h(-1), and that the membrane was to operate above the critical flux to sustain the necessary rate of cell concentration. The membrane with similar pore size but greater pore density experienced not only lesser degree of total resistance, but also possessed smaller fraction of irreversible resistance. Membrane fouling was mainly attributed to fragmented cells rather than to soluble or extracellular polymeric substances. Furthermore, flux recovery studies demonstrated that membrane relaxation and surface cleaning could partially recover fluxes for both low (6gl(-1)) and high (40gl(-1)) cell densities, whereas backwashing could fully recover fluxes. Calculation of energy consumption and cell harvesting productivity also favoured membrane filtration with backwashing.

Lignocellulosic Biomass Transformations via Greener Oxidative Pretreatment Processes: Access to Energy and Value-Added Chemicals

Anthropogenic climate change, principally induced by the large volume of carbon dioxide emission from the global economy driven by fossil fuels, has been observed and scientifically proven as a major threat to civilization. Meanwhile, fossil fuel depletion has been identified as a future challenge. Lignocellulosic biomass in the form of organic residues appears to be the most promising option as renewable feedstock for the generation of energy and platform chemicals. As of today, relatively little bioenergy comes from lignocellulosic biomass as compared to feedstock such as starch and sugarcane, primarily due to high cost of production involving pretreatment steps required to fragment biomass components via disruption of the natural recalcitrant structure of these rigid polymers; low efficiency of enzymatic hydrolysis of refractory feedstock presents a major challenge. The valorization of lignin and cellulose into energy products or chemical products is contingent on the effectiveness of selective depolymerization of the pretreatment regime which typically involve harsh pyrolytic and solvothermal processes assisted by corrosive acids or alkaline reagents. These unselective methods decompose lignin into many products that may not be energetically or chemically valuable, or even biologically inhibitory. Exploring milder, selective and greener processes, therefore, has become a critical subject of study for the valorization of these materials in the last decade. Efficient alternative activation processes such as microwave- and ultrasound irradiation are being explored as replacements for pyrolysis and hydrothermolysis, while milder options such as advanced oxidative and catalytic processes should be considered as choices to harsher acid and alkaline processes. Herein, we critically abridge the research on chemical oxidative techniques for the pretreatment of lignocellulosics with the explicit aim to rationalize the objectives of the biomass pretreatment step and the problems associated with the conventional processes. The mechanisms of reaction pathways, selectivity and efficiency of end-products obtained using greener processes such as ozonolysis, photocatalysis, oxidative catalysis, electrochemical oxidation, and Fenton or Fenton-like reactions, as applied to depolymerization of lignocellulosic biomass are summarized with deliberation on future prospects of biorefineries with greener pretreatment processes in the context of the life cycle assessment.

A study on developing the indicators of energy conservation and carbon reduction for the business

Green House Gas (GHG) emission has become a critical issue for firms to achieve sustainability. This paper focuses on improving enterprises allocate resource on greening more efficiently and proposes a hybrid MCDM model combining Analytic Hierarchy Process (AHP) and Decision-making Trial and Evaluation Laboratory (DEMATEL) to recognize the crucial criteria which have dependence and causality, and build the network relationship map among all GHG criteria. Eighteen criteria of GHG emission with six dimensions were selected from the literatures and modified by six experts of energy sector. The results showed that improve energy efficiency and reduce energy consumption are recognized to be the most influential dimensions of six. In addition, identifying the causality between six dimensions provide an insight for practitioners utilizing firms resources in GHG emission more effectively.

An analytical investigation of a sequence of unusual springtime ozone episodes over metropolitan Taichung in 2007

This study investigated the potential factors contributing to a series of ozone (O3) episodes in the Taichung metropolis, which occurred during the first half of May 2007. Surface data of the meteorological parameters and air pollutant concentrations, supported by Taiwan Environmental Protection Administration, and vertical data monitored via tethersonde sampling were analysed. The analyses showed that local anthropogenic activities and physical factors such as the sea–air interaction were not the main factors contributing to the O3 events. Excluding these potential causes, the results suggest that, during the aforementioned period, the stronger Mainland High and Pacific Low may have been responsible for the long-range transport of large quantities of O3 from Mainland China to Taiwan. Furthermore, O3 photochemical activity also played an important role in the O3 episodes. The faster consumption of NO lead to a more rapid increase in the O3 concentration.