Jianbo Zhang

Sulfur Hexafluoride (SF6) Emission Estimates for China: An Inventory for 1990–2010 and a Projection to 2020

Sulfur hexafluoride (SF6) is the most potent greenhouse gas regulated under the Kyoto Protocol, with a high global warming potential. In this study, SF6 emissions from China were inventoried for 1990-2010 and projected to 2020. Results reveal that the highest SF6 emission contribution originates from the electrical equipment sector (about 70%), followed by the magnesium production sector, the semiconductor manufacture sector and the SF6 production sector (each about 10%). Both agreements and discrepancies were found in comparisons of our estimates with previously published data. An accelerated growth rate was found for Chinese SF6 emissions during 1990-2010. Because the relative growth rate of SF6 emissions is estimated to be much higher than those of CO2, CH4, and N2O, SF6 will play an increasing role in greenhouse gas emissions in China. Global contributions from China increased rapidly from 0.9 ± 0.3% in 1990 to 22.8 ± 6.3% in 2008, making China one of the crucial contributors to the recent growth in global emissions. Under the examined Business-as-usual (BAU) Scenario, projected emissions will reach 4270 ± 1020 t in 2020, but a reduction of about 90% of the projected BAU emissions would be obtained under the Alternative Scenario.

Polybrominated diphenyl ethers in farmland soils: source characterization, deposition contribution and apportionment.

Polybrominated diphenyl ethers (PBDEs), a group of persistent organic pollutants (POPs), are caused for concern recently due to their adverse health effects and environmental ubiquity. In this study, atmospheric and soil PBDE levels in Taizhou, one of the largest WEEE dismantling areas in the world, were measured, ranging from 884 to 2791 pg m(-3) with an average of 1968 pg m(-3) for atmosphere and 2.96 to 200 ng g(-1)dry weight (dw) with the mean of 65.2 ng g(-1)dw for farmland soils, respectively. The close connection between soil PBDE accumulation and atmospheric deposition was also revealed by the estimation of the annual PBDE deposition flux (3.1 ± 0.9 mg m(-2)a(-1)) and the similarity between deposited congener pattern and soil congener profile. Positive matrix factorization (PMF) was conducted to extract possible sources of farmland soil PBDEs and to calculate their contributions. Based on the measured source profiles of PBDE-related activities, five sources were identified representing WEEE dumping, WEEE dismantling, WEEE open burning, residential waste dismantling, and residential waste open burning. WEEE-related recycling activities contributed primary percentage (52%) to farmland soil PBDE concentration, and open burning was an important pathway for PBDEs entering the environment.

Historical Emissions of HFC-23 (CHF3) in China and Projections upon Policy Options by 2050

Trifluoromethane (CHF3, HFC-23) is one of the hydrofluorocarbons (HFCs) regulated under the Kyoto Protocol with a global warming potential (GWP) of 14 800 (100-year). Chinas past, present, and future HFC-23 emissions are of considerable interest to researchers and policymakers involved in climate change. In this study, we compiled a comprehensive historical inventory (1980-2012) and a projection (2013-2050) of HFC-23 production, abatements, and emissions in China. Results show that HFC-23 production in China increased from 0.08 ± 0.05 Gg/yr in 1980 to 15.4 ± 2.1 Gg/yr (228 ± 31 Tg/yr CO2-eq) in 2012, while actual HFC-23 emissions reached a peak of 10.5 ± 1.8 Gg/yr (155 ± 27 Tg/y CO2-eq) in 2006, and decreased to a minimum of 7.3 ± 1.3 Gg/yr (108 ± 19 Tg/yr CO2-eq) in 2008 and 2009. Under the examined business-as-usual (BAU) scenario, the cumulative emissions of HFC-23 in China over the period 2013-2050 are projected to be 609 Gg (9015 Tg CO2-eq which approximates Chinas 2012 CO2 emissions). Currently, Chinas annual HFC-23 emissions are much higher than those from the developed countries, while it is estimated that by year 2027, Chinas historic contribution to the global atmospheric burden of HFC-23 will have surpassed that of the developed nations under the BAU scenario.

Forecast of Consumption and Emission of HFC-134a Used in the Mobile Air-conditioner Sector in China

Abstract HFC-134a is the most important alternative to CFC-12 used in the mobile air-conditioner sector in China. The consumption of HFC-134a has been increasing rapidly in recent years. It becomes the most consumed HFC in the sector. Selecting 2005 as the base line year, future consumption and emission amounts of HFC-134a are estimated through an analysis of a combined scenario: 1) replacement by non-HFC-134a blends, 2) good practice in servicing, 3) technology promotion, and 4) government policies on control of HFC-134a emissions. The analysis shows that HFC-134a consumption and emissions will continue to increase in the next 10 years. The projected HFC-134a consumption will approach 20,150 t and 34,875 t in 2010 and 2015 respectively, while the estimated emission amounts will reach 16,065 t and 30,186 t (i.e., 21 Mt CO2-eq and 39 Mt CO2-eq emissions) correspondingly. Compared with the business-as-usual scenario, the expected emission reductions in 2010 and 2015 will range between 6.7 Mt CO2-eq and 13.0 Mt CO2-eq. Citation Hu, J., D. Wan, C. Li, et al., 2010: Forecasting of consumption and emission of HFC-134a used in mobile air-conditioner sector in China. Adv. Clim. Change Res., 1, doi: 10.3724/SP.J.1248.2010.00020.

Estimated emissions of chlorofluorocarbons, hydrochlorofluorocarbons, and hydrofluorocarbons based on an interspecies correlation method in the Pearl River Delta region, China.

Although many studies have been conducted in recent years on the emissions of chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs) at the large regional (such as East Asia) and national scales, relatively few studies have been conducted for cities or metropolitan areas. In this study, 192 air samples were collected in the Pearl River Delta (PRD) region of China in November 2010. The atmospheric mixing ratios of six halocarbons were analyzed, including trichlorofluoromethane (CFC-11, CCl3F), dichlorodifluoromethane (CFC-12, CCl2F2), monochlorodifluoromethane (HCFC-22, CHClF2), 1,1-dichloro-1-fluoroethane (HCFC-141b, CH3CCl2F), 1-dichloro-1,1-fluoroethane (HCFC-142b, CH3CClF2), and 1,1,1,2-tetrafluoroethane (HFC-134a, CH2FCF3), and their emissions were estimated based on an interspecies correlation method using HCFC-22 as the reference species. The results showed no significant change in the regional concentration and emission of CFC in the past 10years, suggesting that the continuous regional emission of CFC has had no significant effect on the CFC regional concentration in the PRD region. Concentrations and emissions of HCFCs and HFCs are significantly higher compared to previous research in the PRD region (P<0.05). The largest emission was for HCFC-22, most likely due to its substitution for CFC-12 in the industrial and commercial refrigeration subsector, and the rapid development of the room air-conditioner and extruded polystyrene subsectors. The PRDs ODP-weighted emissions of the target HCFCs provided 9% (7-12%) of the national emissions for the corresponding species. The PRDs GWP-weighted emissions of the target HCFCs and HFC-134a account for 10% (7-12%) and 8% (7-9%), respectively, of the national emissions for the corresponding species, and thus are important contributions to Chinas total emissions.

A 17-fold increase of trifluoroacetic acid in landscape waters of Beijing, China during the last decade

The concentrations of trifluoroacetic acid (TFA) were measured in urban landscape waters, tap water and snows in Beijing, China in 2012. Compared with the 2002 measurements, a 17-fold increase from 23-98ngL(-1) to 345-828ngL(-1) was observed for TFA concentrations in urban landscape waters, and an obvious increase from not detected (n.d.) to 155ngL(-1) occurred to TFA in tap water. By flux estimation between air and water interface, the remarkable increase of TFA was attributable to dry and wet deposition. The quantitative water-air-sediment interaction (QWASI) model simulated TFAs in various environmental media and showed that, over 99% of TFA distributed in water bodies. Our results recommend that measures are needed to control the increase of TFA in China.

Airborne trifluoroacetic acid and its fraction from the degradation of HFC-134a in Beijing, China.

Trifluoroacetic acid (TFA) has been attracting increasing attention worldwide because of its increased environmental concentrations and high aquatic toxicity. Atmospheric deposition is the major source of aquatic TFA, but only a few studies have reported either air concentrations or deposition fluxes for TFA. This is the first study to report the atmospheric concentrations of TFA in China, where an annular denuder and filter pack collection system were deployed at a highly urbanized site in Beijing. In total, 144 air samples were collected over the course of 1 year (from May 2012 to April 2013) and analyzed directly using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) or following derivatization by gas chromatography-mass spectrometry (GC-MS). The annual mean atmospheric concentration of TFA was 1580 ± 558 pg/m(3), higher than the previously reported annual mean levels in Germany and Canada. For the first time, it was demonstrated that maximum concentrations of TFA were frequently observed in the afternoon, following a diurnal cycle and suggesting that a major source of airborne TFA is likely degradation of volatile precursors. Using a deposition model, the annual TFA deposition flux was estimated to be 619 ± 264 μg m(-2) year(-1). Nevertheless, a box model estimated that the TFA deposition flux from the degradation of HFC-134a contributed only 14% (6-33%) to the total TFA deposition flux in Beijing. Source analysis is quite important for future TFA risk predictions; therefore, future research should focus on identifying additional sources.

Emission inventory and provincial distribution of short-chain chlorinated paraffins in China

Chlorinated paraffins (CPs) are used as flame retardants, plasticizers, and metalworking fluids, which have varying contents of toxic short-chain chlorinated paraffins (SCCPs). Based on the study of several relevant production and consumption sectors, this paper classifies the consumption of CPs among sectors and provides an emission inventory and the provincial emission distribution of SCCPs in China in 2010-2014 based on the consumption patterns and emission factors of each sector. The total emissions of SCCPs in China in 2014 were 3083.88tons, with emissions to the atmosphere and water accounting for 894.81tons and 2189.07tons, respectively. The largest emission source was from metalworking fluids, with total emissions of 2459.12tons, of which 756.65tons went to the atmosphere and 1702.47tons to water. Our results show that SCCP emissions were mainly concentrated in the eastern, more developed regions and that Jiangsu Province was the biggest producer in China, with total emissions of 1853.06tons, of which 562.61tons were to the atmosphere and 1290.46tons to water.

Determination of Gaseous and Particulate Trifluoroacetic Acid in Atmosphere Environmental Samples by Gas Chromatography-Mass Spectrometry

Abstract Trifluoroacetic acid (TFA) were determined in air samples by a sampling device composed of annular denuders coupled with a quartz filter, which was efficient for the collection and separation of gaseous and particulate TFA. Gaseous TFA was performed by means of annular denuders coated with alkaline solution, while particulate TFA was absorbed by quartz filters. TFA can be determined by gas chromatography-mass spectrometer after derivatizated with 2,4-difluoroaniline. Calibration curves were linear with correlation coefficients of 0.9991. Detection limit of TFA was 66 ng L −1 , which was 31 pg m −3 when sampling volume was 48 m 3 . Recoveries of the TFA sampling device ranged from 98% to 105% with relative standard deviation (RSD) ≤ 3%. The developed method was applied to the determination of TFA in atmosphere samples collected in Peking University in Beijing in 2012. Total TFA concentrations ranged from 501 to 7447 pg m −3 . Concentrations of gaseous TFA were significantly higher than those of particulate, and the gas-particle partition coefficient of TFA decreased as air temperature rose.

Effects of metal ions on the catalytic degradation of dicofol by cellulase

A new technique whereby cellulase immobilized on aminated silica was applied to catalyze the degradation of dicofol, an organochlorine pesticide. In order to evaluate the performance of free and immobilized cellulase, experiments were carried out to measure the degradation efficiency. The Michaelis constant, Km, of the reaction catalyzed by immobilized cellulase was 9.16 mg/L, and the maximum reaction rate, Vmax, was 0.40 mg/L/min, while that of free cellulase was Km=8.18 mg/L, and Vmax=0.79 mg/L/min, respectively. The kinetic constants of catalytic degradation were calculated to estimate substrate affinity. Considering that metal ions may affect enzyme activity, the effects of different metal ions on the catalytic degradation efficiency were explored. The results showed that the substrate affinity decreased after immobilization. Monovalent metal ions had no effect on the reaction, while divalent metal ions had either positive or inhibitory effects, including activation by Mn2+, reversible competition with Cd2+, and irreversible inhibition by Pb2+. Ca2+ promoted the catalytic degradation of dicofol at low concentrations, but inhibited it at high concentrations. Compared with free cellulase, immobilized cellulase was affected less by metal ions. This work provided a basis for further studies on the co-occurrence of endocrine-disrupting chemicals and heavy metal ions in the environment.