Characterization of Particulate-Phase High Molecular Weight Mono-Carbonyls (C# > 5) and Dicarbonyls in Urban Atmosphere of Xi'an, China

An analytical method to quantify particulate-phase high molecular weight mono-carbonyls (C# &gt; 5) and di-carbonyls has been developed by adopting 2,4-dinitrophenylhydrazine (DNPH) derivatization followed by high performance liquid chromatography/ultra-violet (HPLC/UV) detection. Satisfactory reproducibility and precision of the measurements were achieved. This method was applied to measure the carbonyls in PM2.5 collected on quartz-fiber filters, sampled in Xi&#39;an, China, from 2008 to 2009. Nonanaldehyde was the most abundant compound, followed by octanaldehyde, hexanaldehyde and heptaldehyde, accounting for 40%, 20%, 12% and 11% in the total quantified carbonyls. For dicarbonyls, the concentration of methylglyoxal was much higher than that of glyoxal. The seasonal variations of the particulate-phase mono-carbonyls and dicarbonyls were similar to those in the gas-phase, namely winter &gt; autumn &gt; spring &gt; summer (except octanaldehyde). A strong correlation among those carbonyls was observed in winter, resulting from low temperature partitioning, weaker photochemical reaction, and more primary emission sources. In contrast, in summer, vehicle emissions, cooking emissions and photochemical reactions are the major pollution source in Xi&#39;an.</p

Physical parameters effect on ozone-initiated formation of indoor secondary organic aerosols with emissions from cleaning products

The effect of air exchange rate (ACH), temperature (7), and relative humidity (RH) on the formation of indoor secondary organic aerosols (SOAs) through ozonolysis of biogenic organic compounds (BVOCs) emitted from floor cleaner was investigated in this study. The total particle count (with D(p) of 6-225 nm) was up to 1.2 x 10(3) # cm(-3) with ACH of 1.08 h(-1), and it became much more significant with ACH of 0.36 h(-1) (1.1 x 10(4) # cm(-3)). This suggests that a higher ventilation rate can effectively dilute indoor BVOCs, resulting in a less ultrafine particle formation. The total particle count increased when temperature changed from 15 to 23 degrees C but it decreased when the temperature further increased to 30 degrees C. It could be explained that high temperature restrained the condensation of formed semi-volatile compounds resulting in low yields of SOAs. When the RH was at 50% and 80%, SOA formation (1.1-1.2 x 10(4) # cm(-3)) was the more efficient compared with that at RH of 30% (5.9 x 10(3) # cm(-3)), suggesting higher RH facilitating the initial nucleation processes. Oxidation generated secondary carbonyl compounds were also quantified. Acetone was the most abundant carbonyl compound. The formation mechanisms of formaldehyde and acetone were proposed.</p

Hazardous airborne carbonyls emissions in industrial workplaces in China

A pilot hazardous airborne carbonyls study was carried out in Hong Kong and the Mainland of China. Workplace air samples in 14 factories of various types of manufacturing and industrial operations were collected and analyzed for a panel of 21 carbonyl compounds. The factories can be classified into five general categories, including food processing, electroplating, textile dyeing, chemical manufacturer, and petroleum refinery. Formaldehyde was invariably the most abundant carbonyl compound among all the workplace air samples, accounting for 22.0-44.0% of the total measured amount of carbonyls on a molar basis. Acetone was also found to be an abundant carbonyl in workplace settings; among the selected industrial sectors, chemical manufacturers&#39; workplaces had the highest percentage (an average of 42.6%) of acetone in the total amount of carbonyls measured in air. Benzaldehyde accounted for an average of 20.5% of the total amount of detected carbonyls in electroplating factories, but its contribution was minor in other industrial workplaces. Long-chain aliphatic carbonyls (C-6-C-10) accounted for a large portion (37.2%) of the total carbonyls in food-processing factories. Glyoxal and methylglyoxal existed at variable levels in the selected workplaces, ranging from 0.2% to 5.5%. The mixing ratio of formaldehyde ranged from 8.6 to 101.2 ppbv in the sampled workplaces. The observed amount of formaldehyde in two paint and wax manufacturers and food-processing factories exceeded the World Health Organization (WHO) air quality guideline of 81.8 ppbv. Carcinogenic risks of chronic exposure to formaldehyde and acetaldehyde by the workers were evaluated. The lifetime cancer hazard risks associated with formaldehyde exposure to male and female workers ranged from 2.01x10(-5) to 2.37x10(-4) and 2.68x10(-5) to 3.16x10(-4), respectively. Such elevated risk values suggest that the negative health impact of formaldehyde exposure represents a valid concern, and proper actions should be taken to protect workers from such risks. Implications: Many carbonyl species (e.g., formaldehyde, acetaldehyde, and acrolein) are air toxins and they pose public health risks. The scope of this investigation covers 21 types of carbonyls based on samples collected from 14 different workplaces. Findings of the study will not only provide a comprehensive assessment of indoor air quality with regard to workers&#39; healthy and safety, but also establish a theoretical foundation for future formulation of intervention strategies to reduce occupational carbonyl exposures. No similar study has been carried out either in Hong Kong or the Mainland of China.</p

Characterization of biogenic volatile organic compounds (BVOCs) in cleaning reagents and air fresheners in Hong Kong

Biogenic volatile organic compounds (BVOCs) emitted from cleaning products and air fresheners indoors are prone to oxidation resulting in the formation of secondary pollutants that can pose health risks on residents. In this study, a solid phase microextraction (SPME) coupled with gas chromatography/mass spectrometry (SPME-GC/MS) method was applied for the determination of BVOCs compositions in three categories of cleaning products including floor cleaners (FC), kitchen cleaners (KC) and dishwashing detergents (DD), and also air fresheners (AF). The analysis results demonstrated that chemical composition and concentration of individual BVOC varied broadly with household products in the view of their different functions and scents as indicated on the labels. The concentration of total BVOCs for sample FC1 was the highest up to 4146.0 mu g g(-1), followed by FC2 of 264.6 mu g g(-1) FC4 of 249.3 mu g g(-1) and FC3 of 139.2 mu g g(-1). D-limonene was the most abundant detected BVOCs in KC samples with the chemical composition varying from 19.6 +/- 1.0 to 1513.0 +/- 37.1 mu g g(-1). For dishwashing detergents, only D-limonene was detected and quantified. The BVOCs compositions of air freshener samples are much more complicated. It was estimated that the consumption of floor cleaners contributed 51% of the total BVOCs amount indoors in Hong Kong, followed by air fresheners 42%, kitchen cleaners 5% and dishwashing detergents 2%.</p

Characterization and seasonal variations oflevoglucosan in fine particulate matter in Xi’an, China

PM2.5 (particulate matter with an aerodynamic diameter &lt;2.5 mm) samples (n &frac14; 58) collected every sixth day in Xi&rsquo;an, China, from 5 July 2008 to 27 June 2009 are analyzed for levoglucosan (1,6-anhydro-b-D-glucopyranose) to evaluate the impacts of biomass combustion on ambient concentrations. Twenty-four-hour levoglucosan concentrations displayed clear summer minima and winter maxima that ranged from 46 to 1889 ng m 3, with an average of 428 399 ng m 3. Besides agricultural burning, biomass/biofuel combustion for household heating with straws and branches appears to be of regional importance during the heating season in northwestern China. Good correlations (0.70 &lt; R &lt; 0.91) were found between levoglucosan relative to watersoluble K&thorn;, Cl , organic carbon (OC), elemental carbon (EC), and glyoxal. The highest levoglucosan/OC ratio of 2.3% was found in winter, followed by autumn (1.5%). Biomass burning contributed to 5.1&ndash;43.8% of OC (with an average of 17.6 8.4%).</p

Characteristics of fine particulate non-polar organic compounds in Guangzhou during the 16th Asian Games: Effectiveness of air pollution controls

The concentrations of organic compounds, including n-alkanes and polycyclic aromatic hydrocarbons (PAHs), in fine particles (PM2.5) were measured in an urban area of Guangzhou before, during, and after the 16th Asian Games (9-30 November 2010). Higher average concentrations of n-alkanes and PAHs occurred in the nighttime, presumably due to a restriction on motor vehicle operation during the day and the accumulation of pollutants due to temperature inversions at night. The carbon preference index, contributions of wax n-alkanes, and PAHs diagnostic ratios indicated that the main sources of n-alkanes and PAHs were anthropogenic, especially motor vehicle emissions. The CMAQ model was used to estimate the percentages of biogenic organic aerosol in the total organic aerosol, then the ratios of source marker PAHs to biogenic organic carbon were used to evaluate the air pollution control policies effectiveness during the Asian Games.</p