Toxicity assessment of electrochemical advanced oxidation process-treated groundwater from a gas station with petrochemical contamination.

Electrochemical advanced oxidation process (EAOP) is known for its efficient and fast degradation of organic pollutants in polluted water treatment. In this study, the EAOP using a boron-doped diamond (BDD) anode was applied to treat two-season groundwater samples collected from four sampling wells (GS1 to GS4) with petrochemical contaminants including methyl tert-butyl ether (MTBE), benzene, toluene, chlorobenzene, total organic compounds (TOC), and total petroleum hydrocarbons (TPH) at a gas station in southern Taiwan. Moreover, toxicity tests (ATP, p53, and NF-κB bioassays) were performed to evaluate the biological responses of raw and EAOP-treated groundwater. Results show that the concentrations of chlorobenzene before and after EAOP treatment were all below its method detection limit. High degradation efficiencies were observed for MTBE (100%), benzene (100%), toluene (100%, except that of GS2 in the first season), TPH (94-97%, except that of GS4 in the first season), and TOC (85-99%). Cell viability for both the raw groundwater (81.2 ± 13.5%) and EAOP-treated samples (84.7 ± 11.7%) as detected using the ATP bioassay showed no significant difference (p = 0.715). A mean reduction in the DNA damage (739 to 165 ng DOX-equivalency L-1 (ng DOX-EQ. L-1)) and inflammatory response levels (460 to 157 ng TNFα-equivalency L-1 (ng TNFα-EQ. L-1)) were observed for EAOP-treated samples subjected to p53 and NF-κB bioassays. Overall, the significances of the average degradation efficiency, DNA damage, and inflammatory response before and after groundwater with EAOP treatment was observed to be significant (p < 0.05). p53 and NF-κB bioassays might be applied to assess ecotoxic risk in the environment.

Levels of PCDD/Fs, PBDEs, and PBDD/Fs in Breast Milk from Southern Taiwan.

This study investigates the congener-specific concentrations of polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs), polybrominated dibenzo-p-dioxins/furans (PBDD/Fs), and polybrominated diphenyl ethers (PBDEs) in 25 breast milk samples from southern Taiwan. Most investigated congeners in Taiwanese breast milk are detectable except for PBDD/Fs. The geometric means of PCDD/Fs and PBDEs in the breast milk are 2.44 pg WHO2005-TEQ/g lipid and 2810 pg/g lipid. Several PCDD/F and PBDE congeners were highly correlated to each other like 1,2,3,7,8-PeCDD and 2,3,4,7,8-PeCDF (r = 0.919, p < 0.001). The longest duration of menstruation could be predicted by BDE-153 (ß = 0.252) and 1,2,3,4,6,7,8-HpCDF (ß = 0.345) with adjustment of confounders using a multiple stepwise linear regression model (r = 0.963, p < 0.001).

Characterization of spent nickel-metal hydride batteries and a preliminary economic evaluation of the recovery processes.

UNLABELLED: Valuable metal materials can be recovered from spent nickel-metal hydride (NiMH) batteries. However, little attention has been paid to the metal compositions of individual components of NiMH batteries, although this is important for the selection of the appropriate recycling process. In this study, NiMH batteries were manually disassembled to identify the components and to characterize the metals in each of these. A preliminary economic analysis was also conducted to evaluate the recovery of valuable metals from spent NiMH batteries using thermal melting versus simple mechanical separation. The results of this study show that metallic components account for more than 60% of battery weight. The contents of Ni, Fe, Co, and rare earth elements (REEs) (i.e., valuable metals of interest for recovery) in a single battery were 17.9%, 15.4%, 4.41%, and 17.3%, respectively. Most of the Fe was in the battery components of the steel cathode collector, cathode cap, and anode metal grid, while Ni (>90%) and Co (>90%) were mainly in the electrode active materials (anode and cathode metal powders). About 1.88 g of REEs (Ce, La, and Y) could be obtained from one spent NiMH battery. The estimated profits from recovering valuable metals from spent NiMH batteries by using thermal melting and mechanical processes are 2,329 and 2,531 USD/ton, respectively, when including a subsidy of 1,710 USD/ton. The findings of this study are very useful for further research related to technical and economic evaluations of the recovery of valuable metals from spent NiMH batteries. IMPLICATIONS: The spent nickel-metal hydride (NiMH) batteries were manually disassembled and their components were identified. The metals account for more than 60% of battery weight, when Ni, Fe, Co, and rare earth elements (REEs) were 17.9%, 15.4%, 4.41%, and 17.3%, respectively, in a single battery. The estimated profits of recovering valuable metals from NiMH batteries by using thermal melting and mechanical processing are 2,329 and 2,531 USD/ton, respectively, when including a subsidy of 1,710 USD/ton. These findings are very useful to develop or select the recovery methods of valuable metals from spent NiMH batteries.

Degradation of N,N-diethyl-m-toluamid (DEET) on lead dioxide electrodes in different environmental aqueous matrixes.

This study investigates the electrochemical degradation of N,N-diethyl-m-toluamide (DEET) on PbO2 and Bi-PbO2 anodes. The difference in electrode crystalline structure was responsible for the better DEET degradation and TOC removal on PbO2 than on Bi-PbO2. In 1 M Na2SO4, the degradation efficiency and apparent rate constant (kapp) of DEET oxidation on PbO2 increased with the increase in current density or temperature (activation energy=24.4 kJ mol(-1)). The kapp values in DEET-spiked environmental matrixes (municipal wastewater treatment plant secondary effluent (MWTPSE), groundwater (GW), and river water (RW)) were the same (6.05×10(-4) s(-1)), but significantly smaller than that in 1 M Na2SO4 (2.23×10(-3) s(-1)). The TOC removal efficiency was better in MWTPSE than in RW and GW; however, the mineralization current efficiencies in MWTPSE and RW were similar but higher than that in GW. During electrolysis, the aromaticity was lower in GW than in RW.

Evaluation of effect of reducing additives during vitrification via simulation and experiment.

This study investigates how reducing additives governed the vitrification of prepared specimens. In the experiments, pure CaO/CaCO3 and SiO2 served as the major components of glassy matrix (basicity = mass ratio of CaO/SiO2 = 2/3) with doping of hazardous metals (Cr Cu, and Ni). The substitution ratio of CaCO3 for CaO was used as an operating parameter. The specimens were vitrified at 1400 degrees C and a sequential extraction protocol was used to determine the phase distribution of Cr, Cu, and Ni. The volume fractions of crystalline and amorphous phases were measured using semiquantitative x-ray diffraction (XRD) analysis. A commercial software package (HSC Chemistry 6.0) was used to simulate the experiment to acquire additional information. The simulation results showed the addition of CaCO3 generated CO and CO2 at high temperature. This reducing atmosphere might enhance Cu and Ni to be easily separated from slags and elevated the levels of Cu and Ni in ingots. At higher CaCO3 mol(%), the polymerization of silicate (from sorosilicate to inosilicate) in slag rose and the CaSiO3 amount increased. In addition, the immobilization of metals and the acid resistance of slags were improved. The results indicate that CaCO3 addition is favorable for increasing the metal level in ingots and the metal encapsulation in slag in vitrification.

Recovery of valuable metals from electroplating sludge with reducing additives via vitrification.

In this study, vitrification was applied to treat Ni-Cu electroplating sludge. The sludge was mixed with additives (limestone:cullet = 4:6) and then heated to 1450 °C. The cooled product could be separated into slag and ingot. An atomic absorption spectrometer was used to determine the metal levels of specimens and toxicity characteristic leaching procedure (TCLP) tests, whereas the crystalline and surface characteristics were examined using quantitative X-ray diffraction (XRD) analysis and scanning electron microscopy, respectively. With a glassy structure, the slag was mainly composed of Ca, Si, and Mg. The TCLP results of slags met the Taiwan regulated standards, suggesting that slag can be used for recycling purposes. With the aid of additives, the crystalline phase of slag was transformed form CaMgSiO4 into CsSiO3. The ingots were mainly composed of Ni (563,000-693,800 mg/kg), Cu (79,900-87,400 mg/kg), and Fe (35,000-43,600 mg/kg) (target metals) due the gravity separation during vitrification. At appropriate additives/sludge ratios (>0.2), >95% of target metals gathered in the ingot as a recoverable form (Ni-Fe alloy). The high Ni level of slag suggests that the ingot can be used as the raw materials for smelters or the additives for steel making. Therefore, the vitrification approach of this study is a promising technology to recover valuable metals from Ni-Cu electroplating sludge.

Effects of NH4⁺ on Ce(IV) electro-regeneration in simulated and real spent TFT-LCD Cr-etching solutions.

This investigation studies the electro-regeneration of Ce(IV) from Ce(III) in 4 M HNO(3) in the presence/absence of NH(4)(+) and real spent thin-film transistor liquid-crystal display (TFT-LCD) Cr-etching solutions. On Pt, at 2 A and 70 °C for 100 min, the Ce(IV) yield and apparent rate constant of Ce(III) oxidation in 4 M HNO(3) without NH(4)(+) were 100% and 5.54 × 10(-4) s(-1), respectively (and the activation energy was 13.1 kJ mol(-1)). Cyclic voltammetric and electrolytic measurements consistently support the noticeable inhibition by NH(4)(+) of Ce(III) oxidation and lowering of the Ce(IV) yield, respectively. The apparent diffusion coefficients for 0.2 and 0.02 M Ce(III) oxidation in 4 M HNO(3) that contained 0-0.6 M NH(4)(+) were (0.38-0.25) × 10(-5) and (1.6-0.9) × 10(-5) cm(2) s(-1), respectively. Because of combined effects of NH(4)(+) and anion impurities, the 100 min Ce(IV) yield of a real spent TFT-LCD Cr-etching solution (with [NH(4)(+)]/[Ce(III)] = 0.74 M/0.39 M) was 82%, lower than that of 4 M HNO(3) without NH(4)(+), but higher than those of 4 M HNO(3) that contained anion impurities with/without 0.4 M NH(4)(+).

An electrochemical approach to simultaneous determination of acetaminophen and ofloxacin.

This study presents a simple electrochemical approach for preparing a poly(L-serine) film-modified glassy carbon electrode, which responds quickly and sensitively during the simultaneous determination of acetaminophen and ofloxacin in prepared, environmental, and pharmaceutical samples. The prepared electrode exhibited catalytic activities and promoted the oxidation of acetaminophen and ofloxacin. Acetaminophen and ofloxacin showed linear responses between 1.0 × 10(-5) and 1.0 × 10(-4) mol/L and their limits of detection were 1.2 × 10(-7) and 1.6 × 10(-7) mol/L, respectively. The average recoveries (± relative standard deviations) of acetaminophen and ofloxacin were 96.8 ± 3.5 % and 97.6 ± 3.2 %, respectively, indicating that the prepared electrode and detection method are very accurate and reproducible for the simultaneous determination of acetaminophen and ofloxacin.

Characteristics of particulate emissions from a diesel generator fueled with varying blends of biodiesel and fossil diesel.

This study investigated the particulate matter (PM), particle-bound carbons, and polycyclic aromatic hydrocarbons (PAHs) emitted from a diesel-engine generator fuelled with blends of pure fossil diesel oil (D100) and varying percentages of waste-edible-oil biodiesel (W10, 10 vol %; W20, 20 vol %; W30, 30 vol %; and W50, 50 vol %) under generator loads of 0, 1.5, and 3 kW. On average, the PM emission factors of all blends was 30.5 % (range, 13.7-52.3 %) lower than that of D100 under the tested loads. Substituting pure fossil diesel oil with varying percentages of waste-edible-oil biodiesel reduced emissions of particle-bound total carbon (TC) and elemental carbon (EC). The W20 blend had the lowest particle-bound organic carbon (OC) emissions. Notably, W10, W20, and W30 also had lower Total-PAH emissions and lower total equivalent toxicity (Total-BaP(eq)) compared to D100. Additionally, the brake-specific fuel consumption of the generator correlated positively with the ratio of waste-edible-oil biodiesel to pure fossil diesel. However, generator energy efficiency correlated negatively with the ratio of waste-edible-oil biodiesel to pure fossil diesel.

Effect of traffic loading on particle-bound water-soluble ions and carbons collected near a busy road and at an urban site.

This study examines size-resolved particle-bound water-soluble ions and carbons (element carbon (EC) and organic carbon (OC)) collected near a busy road and at an urban site. The traffic-related fine and coarse particles were collected using two manual dichotomous samplers (Dichots) equipped with Quartz filters. The PM(2.5)/PM(2.5-10) value during rush hour (3.57) exceeded that during slack time (2.72). During weekdays and weekends, although the roadside PM(2.5) concentration correlated well with traffic flow (R(2)= 0.91 and 0.81, respectively), the roadside PM(2.5-10) concentration did not. The lowest second aerosol concentrations were observed from 19:00 to 21:00 during weekdays and weekends. The average content of total water-soluble ions in PM(2.5) was 30.7% and 35.7% for weekday and weekend samples, respectively (a total average of 33.2%). In PM(2.5), the content of NO(3)(-) (8.95-11.0%) exceeded that of SO(4)(2-) (7.08-8.10%) at the roadside site. Conversely, the content of PM(2.5)-bound SO(4)(2-) was higher than that of PM(2.5)-bound NO(3)(-) at the urban site. The mean content of PM(2.5)-bound TC was 35.8%, while that of PM(2.5-10)-bound TC was 15.9%. Moreover, the R(2) values of traffic flow versus PM(2.5)-bound EC concentration on weekdays and weekends were 0.89 and 0.56, respectively, and were 0.82 and 0.38, respectively, for those of traffic flow versus PM(2.5)-bound OC concentration.

Preoperative Platelet-to-Lymphocyte Ratio Is Not Associated With Postoperative Atrial Fibrillation.

BACKGROUND: Postoperative atrial fibrillation (POAF) is a common complication after coronary artery bypass grafting (CABG) and is associated with increased short-term and long-term mortality. While the precise etiology of POAF remains unclear, inflammation is a known contributing factor. Preliminary studies have suggested that an elevated preoperative platelet-to-lymphocyte ratio (PLR), an inexpensive and readily available novel inflammatory biomarker, may be associated with increased incidence of POAF after CABG. This study sought to further investigate this hypothesis. METHODS: The study cohort included all patients undergoing isolated CABG, with no prior history of arrhythmia, who were operated on between August 1, 2010, and December 31, 2018, at a major Australian tertiary center (n = 1457). Patients were divided into low (<86) or high (≥86) PLR groups based on an optimal cutoff derived from receiver-operating characteristic curve analysis. The incidence of POAF was then compared. Categorical variables were analyzed using the chi-square test and continuous variables using logistic regression. RESULTS: Of 1457 patients, 495 (34.0%) developed POAF. There was no statistically significant difference in the incidence of POAF between patients in the high-PLR and low-PLR groups (34.8% vs 31.0%; P = .22). Using multivariable logistic regression analysis, high PLR was not independently associated with POAF (odds ratio, 1.04; P = .78). CONCLUSIONS: Elevated preoperative PLR is not independently associated with POAF in patients undergoing isolated CABG. The findings of this study differ from those of 2 previous smaller studies.

Characterization of polychlorinated dibenzo-p-dioxin/dibenzofuran emissions from joss paper burned in a furnace with air pollution control devices.

Burning joss paper, a common practice in temples in some Asian countries, can release toxic pollutants. This study investigated polychlorinated dibenzo-p-dioxin/dibenzofuran (PCDD/F) emissions and profiles from burning joss paper in a temple furnace connected to two wet scrubbers. The mean total PCDD/F content and corresponding toxic equivalent quantity (TEQ) in joss paper were 193 ng kg(-1) and 0.645 ng I-TEQ kg(-1), respectively, whereas those in bottom ash from burned joss paper were 18.5 ng kg(-1) and 1.92 ng I-TEQ kg(-1), respectively. The wet scrubbers decreased individual PCDD/F emissions by 26.7-71.0% and those of total PCDD/Fs and I-TEQ by 47.2% and 66.0%, respectively. The total PCDD/F TEQ emission factors before and after the wet scrubbers were 8.14 and 3.42 microg I-TEQ ton-feedstock(-1), respectively. The estimated total PCDD/F and corresponding TEQ emissions were 5.29 g year(-1) and 0.462 g I-TEQ year(-1), respectively, in Taiwan. Burning joss paper in temple furnaces is a significant source of PCDD/F emissions.

Residue Levels of Organochlorine Pesticides in Breast Milk and Its Associations with Cord Blood Thyroid Hormones and the Offspring's Neurodevelopment.

Previous studies have demonstrated that organochlorine pesticide (OCP) exposure has a negative impact on the neurological function of infants. Only a few reports have investigated the thyroid and growth hormones and their relationship to neurodevelopment after human exposure to OCPs, especially in the case of infants. Our goal was to determine whether breastmilk OCP residues were associated with negative impacts and/or alterations in the neurodevelopment of infants among specific southern Taiwanese mother-breastfed infant pairs. Our subjects (n = 55 pairs) were recruited from southern Taiwan between 2007 and 2010. The thyroid and growth hormone levels in the cord blood samples collected after childbirth were determined. The breastmilk was gathered within one month after childbirth for the determination of OCP levels using a high-resolution gas chromatograph with mass spectrometry, and the neurodevelopment of 10-12-month-old infants was examined using the Bayley Scales of Infant and Toddler Development®, Third Edition (Bayley-III). It was observed that 4,4'-dichlorodiphenyl-dichloroethylene (4,4'-DDE) (mean = 10.3 ng/g lipid) was the most predominant OCP compound in the breastmilk samples. At higher concentrations (>75th percentile), specific OCPs were associated with significantly lower levels of thyroid and growth hormones than at lower concentrations (<75th percentile). Significantly higher odds ratios (ORs) were observed for binary cognitive (OR = 8.09, p = 0.025 for 4,4'-DDT), language (OR = 11.9, p = 0.013 for 4,4'-DDT) and social-emotional (OR = 6.06, p = 0.01 for trans-CHL) composite scores for specific OCPs belonging to the lower exposure group as compared to the higher OCP exposure group. The five domain Bayley-III infant neurodevelopment outcomes were negatively associated with specific OCPs in the breast milk samples based on the redundancy analysis (RDA) test. Bayley-III scales, which include cognitive, language, motor, social-emotional, and adaptive behavior scales, could be predicted by 4,4'-DDT, endrin, endosulfan I, heptachlor, or heptachlor epoxide using multivariate linear regression models with adjustment for maternal age, pre-pregnant BMI, parity, and infant gender. In conclusion, although our study showed that postnatal exposure to breast milk OCPs may be associated with infant neurodevelopmental outcomes and that prenatal exposure, if extrapolated from breastmilk levels, is associated with changes in thyroid and growth hormones that may have effects on neurodevelopment, these associations are only suggestive; thus, further studies are recommended for confirmation.

Reaction efficiencies and rate constants for the goethite-catalyzed Fenton-like reaction of NAPL-form aromatic hydrocarbons and chloroethylenes.

The contaminants present as nonaqueous phase liquids (NAPLs) in the subsurface are long-term sources for groundwater pollution. Fenton-like reaction catalyzed by natural iron oxides such as goethite in soils is one of the feasible in situ chemical reactions used to remediate contaminated sites. This research evaluated the Fenton-like reaction of five chlorinated ethylenes and three aromatic hydrocarbons using goethite as the catalyst. The reaction efficiencies and rate constants of these compounds in NAPL and dissolved forms were compared. The content of goethite used in batch experiments was in the range similar to those found in subsurfaces. Low H2O2 concentrations (0.05 and 0.1%) were tested in order to represent the low oxidant concentration in the outer region of treatment zone. The results showed that at the tested goethite and H2O2 ranges, the majority of contaminants were removed in the first 120 s. When aromatics and chloroethylenes were present as NAPLs, their removal efficiencies and reaction constants decreased. The removal efficiencies of 0.02 mmol NAPL contaminants were 26-70% less than those of the dissolved. The measured rate constants were in the order of 10(9) M(-1) s(-1) for dissolved chlorinated ethylenes and aromatic hydrocarbons, but were 25-60% less for their NAPL forms. The initial dosage of H2O2 and NAPL surface areas (18.4-38.2 mm2) did not significantly affect reaction efficiencies and rate constants of chlorinated NAPLs. Instead, they were related to the octanol-water partition coefficient of compounds. For both dissolved and NAPL forms, aromatic hydrocarbons were more reactive than chlorinated ethylenes in Fenton-like reaction. These results indicated that the decrease in reaction efficiencies and rate constants of NAPL-form contaminants would pose more negative impacts on the less reactive compounds such as benzene and cis 1,2-DCE during goethite-catalyzed Fenton-like reaction.

Anion effects on the electrochemical regeneration of Ce(IV) in nitric acid used for etching chromium.

The anion impurities such as SO4(2-), Cl(-), and Cr2O7(2-) commonly present in the spent (hazardous) Cr-etch solutions from color filter manufacturing processes may influence the solutions' regeneration by the electrooxidation of Ce(III) to Ce(IV). This study, therefore, investigated the effects of these anions on Ce(III)/Ce(IV) redox reactions at glassy carbon in HNO3. In cyclic voltammetric tests, the presence of SO4(2-) decreased the formal potential but increased the peak potential separation (Delta Ep) of Ce(III)/Ce(IV) couple, and lowered the peak current for Ce(IV) reduction whereas Cl(-) did not change the formal potential and Delta Ep, but the peaks for Cl(-) and Ce(III) oxidation partially overlapped. Cr2O7(2-) slightly lowered the peak current for Ce(III) oxidation but significantly decreased that for Ce(IV) reduction. The Tafel slope for Ce(III) oxidation was approximately 65mVdecade(-1) in the absence of anion impurities. Increasing SO4(2-), Cl(-), or Cr2O7(2-) in solution raised the Tafel slope. The Ce(III)/Ce(IV) equilibrium potential decreased with the increase of SO4(2-) or Cl(-) but was hardly influenced by Cr2O7(2-) addition. These observations from individual anion species together well explained the anions' co-effect (kinetic hindrance) on the Ce(III) oxidation in HNO3, revealing that these anions are unfavorable for the electrooxidation of Ce(III) in the spent Cr-etch solutions.

Metal recovery from spent hydrodesulfurization catalysts using a combined acid-leaching and electrolysis process.

This study focuses on recovering valuable metals from spent hydrodesulfurization (HDS) catalysts using a combined acid-leaching and fluidized-bed electrolysis process. The electrolytic cell was equipped with a glass bead medium, an iridium oxide mesh anode, and a stainless steel plate cathode. An acid solution consisting of concentrated HNO3/H2SO4/HCl with a volume ratio of 2:1:1 was found to be better than the other tested solution (HNO3/H2SO4=1:1) to leach the metals. For the three-acid mixture, the best solid/liquid ratio and leaching time were 40 g/L and 1 h, respectively, at 70 degrees C; under this condition, the leaching yields of target metals (Mo, Ni, and V) in the 1st stage of leaching reached 90, 99, and 99%, respectively, much higher than those in the 2nd/3rd/4th stages. When this acid leachate was electrolyzed for 2 h at 2 A constant current (current density=approximately 35.7 mA/cm2), a stable cell voltage of 5 V was observed. The electrolytic recoveries of Mo, Ni, and V were approximately 15, 61, and 66%, respectively, but extending the electrolysis time from 2 to 4 h did not increase the recoveries. For this operation, the total recoveries (leaching yieldxelectrolytic recovery) of Mo, Ni, and V were approximately 14, 60, and 65%, respectively.

Association between Organochlorine Pesticide Levels in Breast Milk and Their Effects on Female Reproduction in a Taiwanese Population.

Only few studies have focused on organochlorine pesticides (OCPs) in breast milk and the related health risks for women in Taiwan. Our goal is to examine breast milk OCPs and their associations with female reproductive function (infertility, gynecological diseases, and menstruation characteristics) as well as their correlation with sociodemographic parameters (age, pre-pregnant body mass index (BMI), annual incomes, population, birth year, and parity) and dietary habit. The breast milk samples were collected in southern Taiwan (n = 68) from 2013 to 2016 and the OCP residues were analyzed using high resolution gas chromatography with low resolution mass spectrometry (HRGC/LRMS). The results show that the most abundant OCP residues in the breast milk was ΣDDT with the geometric mean ± standard deviation of 9.81 ± 7.52 ng−1 lipid−1 followed by ΣHCH (0.539 ± 0.557 ng−1·lipid−1). In the principal component analysis, cis-chlordane (cis-CHL) and γ-HCH were found to be related to participants who received medical treatment for infertility, and 4,4′-DDT was associated with those who received gynecological surgery. The logistic regression showed that the odds ratio (OR) of log γ-hexachlorocyclohexane (γ-HCH) was higher for mothers who had received medical treatment for infertility than for the normal group (OR = 25.6, p = 0.035) after adjustments for age, pre-pregnant BMI, annual income, population (i.e., native-born Taiwanese), birth year, and parity. Cow milk and beef consumption as well as menstruation characteristics such as average menstrual period (>5 days), shortest menstrual period (<3 days), and women who had taken hormonal drugs were significantly associated to several OCP residues in the breast milk. In addition, ΣHCH including β-HCH and γ-HCH was correlated with annual family income and gravidity as well as cow milk and beef consumptions. Overall, γ-HCH exhibited a probable association with the infertility diseases of Taiwanese women, and dietary habit might play an important role in the female Taiwanese exposure to OCPs.

Water-soluble ions in nano/ultrafine/fine/coarse particles collected near a busy road and at a rural site.

This study investigated water-soluble ions in the sized particles (particularly nano (PM(0.01-0.056))/ultrafine (PM(0.01-0.1))) collected using MOUDI and Nano-MOUDI samplers near a busy road site and at a rural site. The analytical results demonstrate that nano and coarse particles exhibited the highest (16.3%) and lowest (8.37%) nitrate mass ratios, respectively. The mass ratio of NO(3)(-) was higher than that of SO(4)(2-) in all the sized particles at the traffic site. The secondary aerosols all displayed trimodal distributions. The aerosols in ultrafine particles collected at the roadside site exhibited Aitken mode distributions indicating they were of local origin. This finding was not observed for those ultrafine particles collected at the rural site. The mass median diameters (MMDs) of the nano, ultrafine, and fine particles were smaller at the traffic site than at the rural site, possibly related to the contribution of mobile engine emissions.

Emissions of polycyclic aromatic hydrocarbons from thermal pre-treatment of waste hydrodesulfurization catalysts.

Despite increasing environmental concerns and stringent limitations on the sulfur content in fuels, many waste hydrodesulfurization (HDS) catalysts containing Co, Mo, Ni and V are generated in the petroleum refining process. To recover valuable metals in the waste HDS catalysts via hydrometallurgy, thermal treatment is usually performed first to remove contaminants (residual oil, carbon and sulfur) present on the surface of catalysts. In this study, the mass partitions of polycyclic aromatic hydrocarbons (PAHs) in different media (aqueous, particulate and gaseous) were quantified in order to determine the efficiency of three different air pollution control devices, cooling unit, filter and glass cartridge, on PAH removal. An afterburner and two furnace temperatures were used to observe the effect on the PAH contents of the treated residues. Results show that total-PAH content in treated residues decreased with the pyrolysis temperature of the primary furnace, while those generated in flue gases were destroyed by the afterburner at an efficiency of approximately 95%. In addition, the thermal process converts high molecular weight PAHs to low molecular weight PAHs, and the afterburner temperature involved (1200 degrees C) was high enough to prohibit the generation of high molecular weight PAHs (HM-PAHs), leading to the domination of low molecular weight PAHs (LM-PAHs) in flue gases, while treated residues were dominated by HM-PAHs. Finally, information on metal contents and their concentrations in the Toxicity Characteristic Leaching Procedure in waste HDS catalyst and thermal treated residues are examined as an index of the potential for metal recovery.

Effect of raw materials on emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from the stack flue gases of secondary aluminum smelters.

The present study was undertaken to investigate the effect of raw materials on PCDD/F emission from secondary aluminum smelters (ALS). Four plants each of aluminum ingot smelters (over 50% ingot) and secondary ALS (over 70% waste or recycled aluminum) were selected and the results compared. The secondary ALS yield much higher PCDD/Fs than the aluminum ingot smelters, or 7.94-22.76ng/Nm(3) versus 0.57-2.67ng/Nm(3), due to the large percentage of waste or recycled aluminum used. As for air pollution control devices (APCDs), the wet scrubber system in one of the aluminum ingot smelters exhibits an adverse effect on PCDD/F removal, due to the continuous recycle of the contaminated water through the scrubber system. Another ingot plant equipped with cartridge filter, there is a significant reduction in PCDD/F TEQ (52%). The powdered activated carbon injection at 2kg/h (110mg/Nm(3)) in one ALS reduces 70% of the total PCDD/Fs. The average emission factor of four secondary ALS is much higher than that of aluminum ingot smelters, or 20-fold higher based on either raw materials or product. Consequently, more attention should be paid to the emission reduction of PCDD/Fs from the secondary ALS, including installation of a secondary burner, additional APCDs and the pre-cleaning of raw materials.