Nitrogen Adsorption and Characteristics of Iron, Cobalt, and Nickel Oxides Impregnated on SBA-15 Mesoporous Silica.

Hexagonal SBA-15 mesoporous material was used as a catalytic template for impregnation, with the transition metals Fe, Co, and Ni as catalysts for chemical transformation. Nitrogen adsorption/desorption isotherms, scanning electron microscopy, and transmission electron microscopy were conducted to better understand the physicochemical properties of the metal oxide-impregnated SBA-15. The specific surface area of the original SBA-15 was approximately 680 m2/g, and the abundances of the catalysts impregnated ranged from 2 to 8%, corresponding to specific surface areas of 560-470 m2/g for Fe-SBA-15, 440-340 m2/g for Ni-SBA-15, and 410-340 m2/g for Co-SBA-15. The increase in impregnated metal loadings filled the pores and collapsed the silica walls during the metal oxides impregnation on SBA-15 and calcination procedures, resulting in a decrease in the specific surface area and pore volume of the templates. The results showed that the order of nitrogen adsorbed was SBA-15 > Fe-SBA-15 > Ni-SBA-15 > Co-SBA-15 when the metal loading was 5%. In addition, the metal oxides on SBA-15 increased the wall thickness compared with raw SBA-15. Based on the XRD spectrum analysis, Fe2O3, Co3O4, and NiO were the stable crystals on the Fe-SBA-15, Co-SBA-15, and Ni-SBA-15, respectively. The sequence of the average grain size of metal oxides on SBA-15 was Co-SBA-15 > Fe-SBA-15 > Ni-SBA-15, according to XRD spectra and Scherrer's equation. Isopropanol could be decomposed by metal oxide-impregnated SBA-15 to form carbon filament materials. Therefore, these materials have the potential to be employed for pollutant removal, catalytic reactions for organic solvent and bio-oil/biomass reforming, and recycling waste into high-value materials.

The effect of microwave pyrolysis on product characteristics and bromine migration for a non-metallic printed circuit board.

At present, it is necessary to carry out environmentally friendly treatment of non-metallic fractions (NMFs) of waste printed circuit board (WPCB) to improve resource utilization. NMFs of WPCB are pyrolyzed by microwave heating to determine the effect of different operating conditions on the characteristics of pyrolysis products. The results show that yields for residue, oil and gas are 59.03-67.63, 7.10-28.46 and 4.86-33.88 wt%. A high temperature promotes a decrease in oil yield and an increase in non-condensable gas yield. An increase in the NaOH dose results in a more significant cracking of the oil to gas. Increasing the concentration of NaOH increases the mass fraction of the total Br in residues (from 23.62 to 86.94 %), so the addition of NaOH is beneficial to the fixation of Br. A kinetics study shows that there are two thermal decomposition regions (398-625 K and 675-925 K), and NaOH-catalyzed pyrolysis reduces the activation energy to 18.91 and 31.95 kJ mol-1, respectively. The formation of Br-containing substances in the pyrolysis oil and gas can be inhibited if the bromine fixation in pyrolysis residue increases. NaOH-catalyzed pyrolysis can reduce bromine and also reduce energy recovery efficiency. This pyrolysis process still requires further research to improve the recovery of energy and valuable materials.

Protection against Ultraviolet A-Induced Skin Apoptosis and Carcinogenesis through the Oxidative Stress Reduction Effects of N-(4-bromophenethyl) Caffeamide, A Propolis Derivative.

Ultraviolet A (UVA) is a major factor in skin aging and damage. Antioxidative materials may ameliorate this UV damage. This study investigated the protective properties of N-(4-bromophenethyl) caffeamide (K36H) against UVA-induced skin inflammation, apoptosis and genotoxicity in keratinocytes. The protein expression or biofactor concentration related to UVA-induced skin damage were identified using an enzyme-linked immunosorbent assay and western blotting. K36H reduced UVA-induced intracellular reactive oxygen species generation and increased nuclear factor erythroid 2-related factor 2 translocation into the nucleus to upregulate the expression of heme oxygenase-1, an intrinsic antioxidant enzyme. K36H inhibited UVA-induced activation of extracellular-signal-regulated kinases and c-Jun N-terminal kinases, reduced the overexpression of matrix metalloproteinase (MMP)-1 and MMP-2 and elevated the expression of the metalloproteinase-1 tissue inhibitor. Moreover, K36H inhibited the phosphorylation of c-Jun and downregulated c-Fos expression. K36H attenuated UVA-induced Bax and caspase-3 expression and upregulated antiapoptotic protein B-cell lymphoma 2 expression. K36H reduced UVA-induced DNA damage. K36H also downregulated inducible nitric oxide synthase, cyclooxygenase-2 and interleukin-6 expression as well as the subsequent generation of prostaglandin E2 and nitric oxide. We observed that K36H ameliorated UVA-induced oxidative stress, inflammation, apoptosis and antiphotocarcinogenic activity. K36H can potentially be used for the development of antiphotodamage and antiphotocarcinogenic products.

Residue characteristics of sludge from a chemical industrial plant by microwave heating pyrolysis.

Sludge from biological wastewater treatment procedures was treated using microwave heating pyrolysis to reduce the environmental impact of a chemical plant. In this study, major elements, trace elements, PAHs and nitro-PAHs in raw sludge, and pyrolysis residues were investigated. The contents of major element from raw sludge were carbon 46.7 ± 5.9%, hydrogen 5.80 ± 0.58%, nitrogen 6.81 ± 0.59%, and sulfur 1.34 ± 0.27%. Trace elemental concentrations including Zn, Mn, Cr, Cd, As, and Sn were 0.410 ± 0.050, 0.338 ± 0.008, 0.063 ± 0.006, 0.019 ± 0.001, 0.004 ± 0.001, and 0.003 ± 0.002 mg/g, respectively. For various pyrolysis temperatures, Ca, Fe, Sr, Cr, and Sn contents remained at almost the same level as those in raw sludge. Results indicated that these elements did not easily volatilize. The content of 16 PAH species was about 4.78 µg/g in the raw sludge and 23-65 µg/g for pyrolysis residues associated with various temperatures. The content of ten nitro-PAHs was about 58 ng/g for the raw sludge and 141-744 ng/g for pyrolysis residues. The total nitro-PAH content was highest at 600 °C and then decreased when the temperature was over 600 °C. Total nitro-PAH content was about 247 ng/g at 800 °C.

Temperature influence on product distribution and characteristics of derived residue and oil in wet sludge pyrolysis using microwave heating.

Sludge taken from a wastewater treatment plant of the petrochemical industry was dewatered and pyrolyzed to produce liquid oil as an alternative fuel via microwave heating. Element contents of dried sludge were 45.9±3.85wt.% carbon, 7.70±1.43wt.% hydrogen, 4.30±0.77wt.% nitrogen and 3.89±0.52wt.% sulfur. Two major thermal degradation peaks of sludge were determined during the microwave pyrolysis process, one at 325-498K (most of the water was vaporized, and the weight loss was over 85wt.%) and the other at 548-898K for sludge constituent decomposition. Zn content was high in the dried raw material and residues. Other toxic elements such as Ni, Cr, Pb, As and Cd contents were 0.61-0.99, 0.18-0.46, 0.15-0.25, 0.018-0.034, and 0.006-0.017mg/g, respectively. About 14-20wt.% of oil was produced based on the dried sludge cake, and the oil major elements were C (69-72wt.%), H (5.7-6.7wt.%), N (1.9-2.2wt.%), and S (0.58-0.82wt.%). The heat values of liquid oils were 8700-9200kcal/kg at 400-800°C.

Water-soluble ionic species of coarse and fine particulate matter and gas precursor characteristics at urban and rural sites of central Taiwan.

Coarse and fine particulate matter (PM) were taken by a dichotomous sampler, and gas precursors were determined by a denuder sampler at two stations in central Taiwan. Water-soluble ionic constituents of PM and their precursor gases were analyzed by ionic chromatograph. In summer, the daytime/nighttime PM10 concentrations were 37 ± 10/41 ± 18 µg m(-3) and 36 ± 14/34 ± 18 µg m(-3) for Xitun and Jhushan, respectively. Average PM10 concentration in winter was 1.55 and 1.76 times that of summer for Xitun and Jhushan, respectively. PM mass concentrations were similar for both stations, although one station is located in the downtown area of Taichung, and the other is in a rural area with no heavy pollution sources. Water-soluble ionic species content was 38-53 % of PM2.5 and 43-48 % of PM10 mass concentration. HNO3, HCl, and SO2 were high in the daytime; the daytime-to-nighttime concentration ratio was 3.75-6.88 for HNO3,1.7-7.8 for HCl, and 1.45-2.77 for SO2. High NH3 levels were determined in the area, especially in winter, which could be a precursor of NH4 (+) to form particulate matter. In Xitun, motor vehicles downtown and in the industrial district could be sources of air pollution. In contrast, there are few industrial sources at Jhushan; therefore, the transport of air pollutants from upwind of other regions and the accumulation of pollutants could be important PM sources at Jhushan.

Characteristics of Carbon Material Formation on SBA-15 and Ni-SBA-15 Templates by Acetylene Decomposition and Their Bioactivity Effects.

Carbon spheres and tubes were formed from acetylene decomposition on SBA-15 and Ni-SBA-15 at 650-850 °C. At 650 °C, the decomposed carbons covered the surface of the support, and no carbon spheres and filament materials were formed. Carbon sphere formation occurred at 750 °C-850 °C; with diameters ranging from 0.8 µm-1.1 µm. For Ni-SBA-15, the diameters of the spheres and filaments were 0.8 µm and 62 nm, respectively, at 650 °C. At 750 °C, the diameter of the ball carbon materials ranged from 0.7 µm-0.8 µm, the diameter of the carbon tubes formed was 120-130 nm, and their pore diameter was 8.0 nm-11 nm. At 850 °C, the diameters of ball carbon materials and carbon tubes were similar to those of the materials at the formation temperature, 750 °C. Si, O and C were the main constituents of SBA-15; Ni-SBA-15 and carbon material formation supports. High-ring PAHs (such as BaP (five rings); IND (six rings); DBA (five rings) and B[ghi]P (six rings)) exist in carbon materials. SBA-15 revealed insignificant cytotoxicity, but Ni-SBA-15 inhibited the proliferation of human lung cancer cells (A549). Less inhibition on cell viability and reactive oxidative species (ROS) generation on A549 were determined for carbon material formation on the Ni-SBA-15 compared to the Ni-SBA-15.

Airborne pollutant characteristics in an urban, industrial and agricultural complex metroplex with high emission loading and ammonia concentration.

The size distribution of particulate mass and water-soluble ionic constituents and their gaseous precursors was investigated in a subtropical area, southern Taiwan. Field sampling and chemical analysis of particulate matter (PM) were conducted using a Micro Orifice Uniform Deposition Impactor (MOUDI) and a Nano-MOUDI, and gaseous pollutants were determined by a denuder-filter pack system. PM size mass distribution, mass concentration and ionic species concentration were measured during the day and at night in the winter and summer. Average PM concentrations in the winter were as high as 132 ± 42 µg/m(3), and PM mass concentrations in the summer were as low as 38 ± 19 µg/m(3). Generally, PM concentration was 111 ± 60 µg/m(3) at night, which was 20% higher than that in the daytime. The size-segregated mass distribution of PM mass concentration was over 85% in the 0.1-3.2 µm range. Ammonium, nitrate, and sulfate were the dominant water-soluble ionic species in PM, contributing 34%-48% of PM mass. High ammonia (12.9-49 µg/m(3)) and SO2 (2.6-27 µg/m(3)) were observed in the gas precursors. The molar ratio [Formula: see text] was 3.18 ± 1.20 at PM1.0, which indicated that the PM was rich in ammonium. Therefore, the excess ammonium could neutralize nitrate to form ammonium nitrate, after the more stable ammonium sulfate and ammonium bisulfate formation.

Carbon material formation on SBA-15 and Ni-SBA-15 and residue constituents during acetylene decomposition.

Carbon materials including carbon spheres and nanotubes were formed from acetylene decomposition on hydrogen-reduced SBA-15 and Ni-SBA-15 at 650-850°C. The physicochemical characteristics of SBA-15, Ni-SBA-15 and carbon materials were analyzed by field emission scanning electronic microscopy (FE-SEM), Raman spectrometry, and energy dispersive spectrometry (EDS). In addition, the contents of polyaromatic hydrocarbons (PAHs) in the tar and residue and volatile organic compounds (VOCs) in the exhaust were determined during acetylene decomposition on SBA-15 and Ni-SBA-15. Spherical carbon materials were observed on SBA-15 during acetylene decomposition at 750 and 850°C. Carbon filaments and ball spheres were formed on Ni-SBA-15 at 650-850°C. Raman spectroscopy revealed peaks at 1290 (D-band, disorder mode, amorphous carbon) and 1590 (G-band, graphite sp(2) structure)cm(-1). Naphthalene (2 rings), pyrene (4 rings), phenanthrene (3 rings), and fluoranthene (4 rings) were major PAHs in tar and residues. Exhaust constituents of hydrocarbon (as propane), H2, and C2H2 were 3.9-2.6/2.7-1.5, 1.4-2.8/2.6-4.3, 4.2-2.4/3.2-1.7% when acetylene was decomposed on SBA-15/Ni-SBA-15, respectively, corresponding to temperatures ranging from 650 to 850°C. The concentrations of 52 VOCs ranged from 9359 to 5658 and 2488 to 1104ppm for SBA-15 and Ni-SBA-15 respectively, at acetylene decomposition temperatures from 650 to 850°C, and the aromatics contributed more than 87% fraction of VOC concentrations.

Liquid oil and residual characteristics of printed circuit board recycle by pyrolysis.

Non-metal fractions of waste printed circuit boards (PCBs) were thermally treated (200-500°C) under nitrogen atmosphere. Carbon, hydrogen, and nitrogen were determined by elemental analyzer, bromine by instrumental neutron activation analysis (INAA), phosphorus by energy dispersive X-ray spectrometer (EDX), and 29 trace elements by inductively coupled plasma atomic emission spectrometer (ICP-AES) and mass spectrometry (ICP-MS) for raw material and pyrolysis residues. Organic compositions of liquid oil were identified by GC (gas chromatography)-MS, trace element composition by ICP system, and 12 water-soluble ions by IC (ionic chromatography). Elemental content of carbon was >450 mg/g, oxygen 300 mg/g, bromine and hydrogen 60 mg/g, nitrogen 30 mg/g, and phosphorus 28 mg/g. Sulfur was trace in PCBs. Copper content was 25-28 mg/g, iron 1.3-1.7 mg/g, tin 0.8-1.0mg/g and magnesium 0.4-1.0mg/g; those were the main metals in the raw materials and pyrolytic residues. In the liquid products, carbon content was 68-73%, hydrogen was 10-14%, nitrogen was 4-5%, and sulfur was less than 0.05% at pyrolysis temperatures from 300 to 500°C. Phenol, 3-bromophenol, 2-methylphenol and 4-propan-2-ylphenol were major species in liquid products, accounting for >50% of analyzed organic species. Bromides, ammonium and phosphate were the main species in water sorption samples for PCB pyrolysis exhaust.

Element and PAH constituents in the residues and liquid oil from biosludge pyrolysis in an electrical thermal furnace.

Biosludge can be pyrolyzed to produce liquid oil as an alternative fuel. The content of five major elements, 22 trace elements and 16 PAHs was investigated in oven-dried raw material, pyrolysis residues and pyrolysis liquid products. Results indicated 39% carbon, 4.5% hydrogen, 4.2% nitrogen and 1.8% sulfur were in oven dried biosludge. Biosludge pyrolysis, carried out at temperatures from 400 to 800°C, corresponded to 34-14% weight in pyrolytic residues, 32-50% weight in liquid products and 31-40% weight in the gas phase. The carbon, hydrogen and nitrogen decreased and the sulfur content increased with an increase in the pyrolysis temperature at 400-800°C. NaP (2 rings) and AcPy (3 rings) were the major PAHs, contributing 86% of PAHs in oven-dried biosludge. After pyrolysis, the PAH content increased with the increase of pyrolysis temperature, which also results in a change in the PAH species profile. In pyrolysis liquid oil, NaP, AcPy, Flu and PA were the major species, and the content of the 16 PAHs ranged from 1.6 to 19 µg/ml at pyrolysis temperatures ranging from 400 to 800°C. Ca, Mg, Al, Fe and Zn were the dominant trace elements in the raw material and the pyrolysis residues. In addition, low toxic metal (Cd, V, Co, and Pb) content was found in the liquid oil, and its heat value was 7,800-9,500 kcal/kg, which means it can be considered as an alternative fuel.

Exhaust constituent emission factors of printed circuit board pyrolysis processes and its exhaust control.

The printed circuit board (PCB) is an important part of electrical and electronic equipment, and its disposal and the recovery of useful materials from waste PCBs (WPCBs) are key issues for waste electrical and electronic equipment. Waste PCB compositions and their pyrolysis characteristics were analyzed in this study. In addition, the volatile organic compound (VOC) exhaust was controlled by an iron-impregnated alumina oxide catalyst. Results indicated that carbon and oxygen were the dominant components (hundreds mg/g) of the raw materials, and other elements such as nitrogen, bromine, and copper were several decades mg/g. Exhaust constituents of CO, H2, CH4, CO2, and NOx, were 60-115, 0.4-4.0, 1.1-10, 30-95, and 0-0.7mg/g, corresponding to temperatures ranging from 200 to 500°C. When the pyrolysis temperature was lower than 300°C, aromatics and paraffins were the major species, contributing 90% of ozone precursor VOCs, and an increase in the pyrolysis temperature corresponded to a decrease in the fraction of aromatic emission factors. Methanol, ethylacetate, acetone, dichloromethane, tetrachloromethane and acrylonitrile were the main species of oxygenated and chlorinated VOCs. The emission factors of some brominated compounds, i.e., bromoform, bromophenol, and dibromophenol, were higher at temperatures over 400°C. When VOC exhaust was flowed through the bed of Fe-impregnated Al2O3, the emission of ozone precursor VOCs could be reduced by 70-80%.

Emission factor of exhaust gas constituents during the pyrolysis of zinc chloride immersed biosolid.

Pyrolysis enables ZnCl2 immersed biosolid to be reused, but some hazardous air pollutants are emitted during this process. Physical characteristics of biosolid adsorbents were investigated in this work. In addition, the constituents of pyrolytic exhaust were determined to evaluate the exhaust characteristics. Results indicated that the pyrolytic temperature was higher than 500 °C, the specific surface area was >900 m(2)/g, and the total pore volume was as much as 0.8 cm(3)/g at 600 °C. For non-ZnCl2 immersed biosolid pyrolytic exhaust, VOC emission factors increased from 0.677 to 3.170 mg-VOCs/g-biosolid with the pyrolytic temperature increase from 400 to 700 °C, and chlorinated VOCs and oxygenated VOCs were the dominant fraction of VOC groups. VOC emission factors increased about three to seven times, ranging from 1.813 to 21.448 mg/g for pyrolytic temperatures at 400-700 °C, corresponding to the mass ratio of ZnCl2 and biosolid ranging from 0.25-2.5.

Characteristics of particulate constituents and gas precursors during the episode and non-episode periods.

UNLABELLED: Size-segregated distribution of ambient particulate matter (PM) was determined using a micro-orifice uniform deposition impactor (MOUDI) and a nano-MOUDI in southern Taiwan. Eleven water-soluble ionic species including six anions (NO3-, SO4(2-), Cl-, F-, NO2-, Br-) and five cations (NH4+, Na+, K+, Ca2+, Mg2+) for particulate inorganic ions and five gaseous pollutants (i.e., HNO2, HNO3, HCl, SO2, NH3) were analyzed during episode and non-episode periods. The particulate mass concentration was about 30 microg/ m3 higher at night than during the day, and it reached 162 microg/m3 during the episode periods. The difference was mainly attributable to the particle size of 0.1-2.5 microm. Nitrate, sulfate, ammonium, and chloride ions were the dominant inorganic ions in PM. HONO and NH3 concentrations were high at night; in contrast, HNO3, HCl, and SO2 were high during the day. The equivalent ratio of {[NO3-] + 2 [SO4(2-)}/[NH4+] was about 0.98 and revealed a high correlation between {[NO3-] + 2[SO4(2-)]} and [NH4+] that clearly pointed to ammonium neutralization or condensation of ammonium nitrate and ammonium sulfate in PM0.32. The precursor gases and ionic species in different particle sizes did not reveal a strong correlation, which could be attributed to the complex of source emissions, atmospheric reactions and meteorological parameters in the area. IMPLICATIONS: Size-segregated distribution and chemical compositions of atmospheric aerosols play important roles in their visibility reduction, health effects, and toxicity in urban areas. Inorganic ionic species are major constituents in particulate matter, except carbonaceous chemicals. In this work, the compositions of water-soluble ions in particulate matter and acid/base gaseous pollutants (such as HNO2, HNO3, HCl, SO2, NH3) were determined during the day and at night during episode and non-episode periods from 2006 to 2007 in southern Taiwan.

Size mass distribution of water-soluble ionic species and gas conversion to sulfate and nitrate in particulate matter in southern Taiwan.

A Micro-Orifice Uniform Deposition Impactor (MOUDI) and a Nano-MOUDI were employed to determine the size-segregated mass distributions of ambient particulate matter (PM) and water-soluble ionic species for particulate constituents. In addition, gas precursors, including HCl, HONO, HNO3, SO2, and NH3 gases, were analyzed by an annular denuder system. PM size mass distribution, mass concentration, and ionic species concentration were measured during the day and at night during episode and non-episode periods in winter and summer. Average total suspended particle (TSP) concentrations during episode days in winter were as high as 153 ± 33 µg/m(3), and PM mass concentrations in summer were as low as one-third of that in winter. Generally, PM concentration at night was higher than that in the daytime in southern Taiwan during the sampling periods. In winter during the episode periods, the size-segregated mass distribution of PM mass concentration was mostly in the 0.32-3.2-µm range, and the PM concentration increased significantly in the range of 0.32-3.2 µm at night. Ammonium, nitrate, and sulfate were the dominant water-soluble ionic species in PM, contributing 34-48% of TSP mass. High concentrations of ammonia (12.9-49 µg/m(3)) and SO2 (2.6-27 µg/m(3)) were observed in the gas precursors. The conversion ratio was high in the PM size range of 0.18-3.2 µm both during the day and at night in winter, and the conversion ratio of episode days was 20% higher than that of non-episode days. The conversion factor was high for both nitrogen and sulfur species at nighttime, especially on episode days.

Exhaust characteristics during the pyrolysis of ZnCl2 immersed biosludge.

Biosludge can be reused as an adsorbent after ZnCl(2) activation, pyrolysis, washing with HCl and distilled water, and drying. But the pyrolysis exhaust of ZnCl(2) immersed sludge can be hazardous to human health and the environment. The chemical composition, including carbon, nitrogen, hydrogen, sulfur and 21 trace elements, as well as the physical characteristics, including specific surface area, pore volume, pore size distribution and pore diameter of pyrolytic residue, were investigated in this work. In addition, the components of pyrolytic exhaust including 30 VOC species and 5 odorous sulfur gases were determined to evaluate the exhaust characteristics. The results indicated that the pyrolytic temperature was higher than 500°C, the specific surface area could be over 900 m(2)/g, and the total pore volume could be up to 0.8 cm(3)/g at 600°C. Exhaust concentration fractions of VOC groups were about 65-71% oxygenated VOCs, 18-21% chlorinated VOCs, 4-6% aromatic VOCs, and 6-10% acrylonitrile and cyclohexane under the specific conditions in this study.

Spatiotemporal variability of submicrometer particle number size distributions in an air quality management district.

First measurements of ambient 10-1000 nm particle number concentrations (N(TOT)) and size distributions were made at an urban, coastal, mountain and downwind site within the Central Taiwan Air Quality Management District during a cold and a warm period. The primary objectives were to characterize the spatial and temporal variability of the size-fractionated submicrometer particles and their relationships with copollutants and meteorological parameters. The results show that the ultrafine particles (<100 nm) are the major contributor to the N(TOT). The mean N(TOT) was highest at the urban site, whereas lower and comparable at the three other sites. Although the mean N(TOT) at each site showed insignificant differences between study periods, their diurnal patterns and size distribution modal characteristics were modestly to substantially different between study sites. Correlation analyses of time-resolved collocated aerosol, copollutants and meteorological data suggest that the observed variability is largely attributable to the local traffic and to a lesser extent photochemistry and SO(2) possibly from combustion sources or regional transport. Despite sharing a common traffic source, the ultrafine particles were poorly correlated with the accumulation particles (100-1000 nm), between which the latter showed strong positive correlation with the PM(2.5) and PM(10). Overall, the N(TOT) and size distributions show modest spatial heterogeneity and strong diurnal variability. In addition, the ultrafine particles have variable sources or meteorology-dependent formation processes within the study area. The results imply that single-site measurements of PM(2.5), PM(10) or N(TOT) alone and without discriminating particle sizes would be inadequate for exposure and impact assessment of submicrometer particle numbers in a region of diverse environments.

Particulate composition characteristics under different ambient air quality conditions.

Particulate compositions including elemental carbon (EC), organic carbon (OC), water-soluble ionic species, and elemental compositions were investigated during the period from 2004 to 2006 in southern Taiwan. The correlation between the pollutant standard index (PSI) of ambient air quality and the various particle compositions was also addressed in this study. PSI revealed a correlation with fine (r = 0.74) and coarse (r = 0.80) particulate matter (PM). PSI manifested a significant correlation with the amount of analyzed ionic species (r approximately 0.80) in coarse and fine particles and a moderate correlation with carbon content (r = 0.63) in fine particles; however, it showed no correlation with elemental content. Although the ambient air quality ranged from good to moderate, the ionic species including chloride (Cl-), nitrate (NO3-), sulfate (SO4(2-)), sodium (Na+), ammonium (NH4+), magnesium (Mg2+), and calcium (Ca2+) increased significantly (1.5-3.7 times for Daliao and 1.8-6.9 times for Tzouying) in coarse PM. For fine particles, NO3-, SO4(2-), NH4+, and potassium (K+) also increased significantly (1.3-2.4 times for Daliao and 2.8-9.6 times for Tzouying) when the air quality went from good to moderate. For meteorological parameters, temperature evidenced a slightly negative correlation with PM concentration and PSI value, which implied a high PM concentration in the low-temperature condition. This reflects the high frequency of PM episodes in winter and spring in southern Taiwan. In addition, the mixing height increase from 980 to 1450 m corresponds to the air quality condition changing from unhealthy to good.

The effect of prenatal perfluorinated chemicals exposures on pediatric atopy.

BACKGROUND: The role of perfluorinated compounds (PFCs) in the immune system and allergic diseases is not well-known. This study examined the effects of pre-natal exposure to PFCs on immunoglobulin E (IgE) levels and atopic dermatitis (AD). METHODS: In Taiwan Birth Panel cohort study, newborns with cord blood and peri-natal factors (i.e. birth body weight, weeks of gestation, and type of delivery) gathered at birth were evaluated. At the age of 2 years, information on the development of AD, environmental exposures, and serum total IgE were collected. The AD and non-AD children were compared for the concentration of cord blood serum PFCs measured by Ultra-performance liquid chromatography/triple-quadrupole mass (UPLC-MS/MS). Correlations among cord blood IgE, serum total IgE at 2 years of age, and cord blood PFC levels were made. RESULTS: Of 244 children who completed the follow-up and specimen collections, 43 (17.6%) developed AD. Concentrations of cord blood serum perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), perfluorononanoic acid (PFNA), and perfluorohexane sulfonic acid (PFHxS) were median (range) 1.71 (0.75-17.40), 5.50 (0.11-48.36), 2.30 (0.38-63.87), and 0.035 (0.035-0.420)ng/mL, respectively. PFOA and PFOS levels positively correlated with cord blood IgE levels (per ln-unit: ß=0.134 KU/l, p=0.047 for PFOA; ß=0.161 KU/l, p=0.017 for PFOS). Analyses stratified by gender revealed that PFOA and PFOS levels positively correlated with cord blood IgE levels only in boys (per ln-unit: ß=0.206 KU/l, p=0.025 for PFOA; ß=0.175 KU/l, p=0.053 for PFOS). When dividing cord blood serum PFCs into quartiles in the fully adjusted models, AD had no significant association with PFOS. CONCLUSIONS: Pre-natal PFOA and PFOS exposures positively correlated with cord blood IgE levels.

Characteristics of exhaust gas, liquid products, and residues of printed circuit boards using the pyrolysis process.

INTRODUCTION: The pyrolytic method was employed to recycle metals and brominated compounds blended into printed circuit boards (PCBs). METHODS: PCBs were crushed into pieces 4.0-4.8 mm in size, and the crushed pieces were pyrolyzed at temperatures ranging from 200 to 500 degrees C. The compositions of pyrolytic residues, liquid products, and exhaust were analyzed by inductively coupled plasma atomic emission spectrometer, inductively coupled plasma mass spectrometry, and gas chromatography-mass spectrometry. Pyrolytic exhaust was collected by an impinger system in an ice bath cooler to analyze the composition fraction of the liquid product, and uncondensable exhaust was collected for gas constituent analysis. RESULTS: Phenol, methyl-phenol, and bromo-phenol were attributed mainly to the liquid product. Metal content was low in the liquid product. In addition, CO, CO(2), CH(4), and H(2) were the major components of pyrolytic exhaust. CONCLUSIONS: Brominated and chlorinated compounds-i.e., dichloromethane, trans-1,2 dichloroethylene, cis-1,2 dichloroethylene, 1,1,1-trichloroethane, tetrachloromethane, bromophenol, and bromoform-could be high, up to the several parts per million (ppm) level. Low molecular weight volatile organic compounds (VOCs)-i.e., methanol, acetone, ethyl acetate, acrylonitrile, 1-butene, propene, propane, and n-butane-contributed a large fraction of VOCs. The concentrations of toluene, benzene, xylene, ethylbenzene, and styrene were in the ppm range.