A mass-balance-based emission inventory of non-methane volatile organic compounds (NMVOCs) for solvent use in China

Non-methane volatile organic compounds (NMVOCs) are important precursors of ozone (O3) and secondary organic aerosol (SOA), which play key roles in tropospheric chemistry. A huge amount of NMVOC emissions from solvent use are complicated by a wide spectrum of sources and species. This work presents a long-term NMVOC emission inventory of solvent use during 2000–2017 in China. Based on a mass (material) balance method, NMVOC emissions were estimated for six categories, including coatings, adhesives, inks, pesticides, cleaners, and personal care products. The results show that NMVOC emissions from solvent use in China increased rapidly from 2000 to 2014 then kept stable after 2014. The total emission increased from 1.6 Tg (1.2–2.2 Tg at 95 % confidence interval) in 2000 to 10.6 Tg (7.7–14.9 Tg) in 2017. The substantial growth is driven by the large demand for solvent products in both industrial and residential activities. However, increasing treatment facilities in the solvent-related factories in China restrained the continued growth of solvent NMVOC emissions in recent years. Rapidly developing and heavily industrialized provinces such as Jiangsu, Shandong, and Guangdong contributed significantly to the solvent use emissions. Oxygenated VOCs, alkanes, and aromatics were the main components, accounting for 42 %, 28 %, and 21 % of total NMVOC emissions in 2017, respectively. Our results and previous inventories are generally comparable within the estimation uncertainties (−27 %–52 %). However, there exist significant differences in the estimates of sub-categories. Personal care products were a significant and quickly rising source of NMVOCs, which were probably underestimated in previous inventories. Emissions from solvent use were growing faster compared with transportation and combustion emissions, which were relatively better controlled in China. Environmentally friendly products can reduce the NMVOC emissions from solvent use. Supposing all solvent-based products were substituted with water-based products, it would result in 37 %, 41 %, and 38 % reduction of emissions, ozone formation potential (OFP), and secondary organic aerosol formation potential (SOAP), respectively. These results indicate there is still large potential for NMVOC reduction by reducing the utilization of solvent-based products and implementation of end-of-pipe controls across industrial sectors.

A mass balance-based emission inventory of non-methane volatile organic compounds (NMVOCs) for solvent use in China

Non-methane volatile organic compounds (NMVOCs) are important precursors of ozone (O3) and secondary organic aerosol (SOA), which play key roles in tropospheric chemistry. A huge amount of NMVOCs emissions from solvent use are complicated by a wide spectrum of sources and species. This work presents a long-term NMVOCs emission inventory of solvent use during 2000–2017 in China. Based on a mass (material) balance method, NMVOCs emissions were estimated for six categories, including coatings, adhesives, inks, pesticides, cleaners and personal care products. The results show that NMVOC emissions from solvent use in China increased rapidly from 2000 to 2014 then kept stable after 2014. The total emission increased from 1.6 Tg (1.2–2.2 Tg at 95 % confidence interval) in 2000 to 10.6 Tg (7.7–14.9 Tg) in 2017. The substantial growth is driven by the large demand of solvent products in both industrial and residential activities. However, increasing treatment facilities on the solvent-related factories in China restrained the continued growth of solvent NMVOCs emissions in recent years. Rapidly developing and heavily industrialized provinces such as Jiangsu, Shandong and Guangdong contributed significantly to the solvent use emissions. Oxygenated VOCs, alkanes and aromatics were main components, accounting for 42 %, 28 % and 21 % of total NMVOCs emissions in 2017, respectively. Our results and previous inventories are generally comparable within the estimation uncertainties (−27 %–52 %). However, there exist significant differences in the estimates of sub-categories. Personal care products were a significant and quickly rising source of NMVOCs, which were probably underestimated in previous inventories. Emissions from solvent use were growing faster compared with transportation and combustion emissions which were relatively better controlled in China. Environmentally friendly products can reduce the NMVOCs emissions from solvent use. Supposing all solvent-based products were substituted by water-based products, it would result in 37 %, 41 % and 38 % reduction of emissions, OFP and SOAP, respectively. These results indicate there is still large room for NMVOCs reduction by reducing the utilization of solvent product and end-of-pipe control across industrial sectors.

Solar absorptive coating: a thermally stable spinel pigment based coating with inorganic binder for waterborne paint

Purpose The spectrally selective solar absorption paint is prepared from spinel-based mixed metal oxides with inorganic binder as a key component. Inorganic binder (furnace cement) is blended with mixed metal oxide pigment during synthesis. High temperature stability upto 1,100ºC is achieved by the use of this modified coating system. The purpose of this paper is to work on solar selective coating synthesis, and application of a coating as a water-borne paint is the additive key feature that helps in reduction of solvent use. Design/methodology/approach The paint was formulated using water-based system, and the main component of colorant was made by mixed metal oxide–based spinel pigment and highly temperature stable inorganic binder. Findings The paint formed shows excellent absorptive power with low emittance even at high temperature. Optical and thermal properties were determined along with adhesion, abrasion and other properties. The solar absorptance for these samples were as = 0.93–0.95 with corresponding thermal emittance of eT = 0.096 (at room temperature) and 0.2–0.22 (at elevated temperature 100°C). Originality/value The paint formed shows excellent absorptive power with low emittance even at high temperature. The paint can be applied in solar absorptive tower system. The obtained results indicated excellent thermal stability of prepared paint coatings. As inorganic binder was used, the paint has reduction in solvent use, and being water as a base, it is environment friendly, easy to apply and durable at high temperatures, as the binder itself is stable up to 1,500ºC.

O3 Sensitivity and Contributions of Different NMHC Sources in O3 Formation at Urban and Suburban Sites in Shanghai

Ground-level ozone (O3) pollution is still one of the priorities and challenges for air pollution control in the Yangtze River Delta (YRD) region of China. Understanding the relationship of O3 with its precursors and contributions of different sources in O3 formation is essential for the development of an O3 control strategy. This study analyzed O3 sensitivity to its precursors using a box model based on online observations of O3, non-methane hydrocarbons (NMHCs), nitrogen oxides (NOx), and carbon monoxide (CO) at an urban site and a suburban site in Shanghai in July 2017. Anthropogenic sources of NMHCs were identified using the positive matrix factorization (PMF) receptor model, and then contributions of different sources in O3 formation were estimated by the observation-based model (OBM). The relative incremental reactivity (RIR) values calculated by the OBM suggest that O3 formation at the urban site was in the NMHC-limited regime, while O3 formation at the suburban site tended between the transition regime and the NMHC-limited regime. Vehicular emission and liquefied petrochemical gas (LPG) use or aged air mass were found to be the two largest contributors at the urban and suburban sites in July, followed by paint and solvent use, and the petrochemical industry. However, from the perspective of O3 formation, vehicular emission and paint and solvent use were the largest two contributors at two sites due to the higher RIR values for paint and solvent use. In addition, the influence of transport on O3 sensitivity was identified by comparing O3 sensitivity at the suburban site across two days with different air mass paths. The result revealed that O3 formation in Shanghai is not only related to local emissions but also influenced by emissions from neighboring provinces. These findings on O3–NMHC–NOX sensitivity, contributions of different sources in O3 formation, and influence of transport could be useful for O3 pollution control in the YRD region. Nevertheless, more quantitative analyses on transport and further evaluation of the uncertainty of the OBM are still needed in future.

Evolution of anthropogenic air pollutant emissions in Guangdong Province, China, from 2006 to 2015

Guangdong Province (GD), one of the most prosperous and populous regions in China, still experiences haze events and growing ozone pollution in spite of the substantial air-quality improvement in recent years. Integrated control of fine particulate matter (PM2.5) and ozone in GD calls for a systematic review of historical emissions. In this study, emission trends, spatial variations, source-contribution variations, and reduction potentials of sulfur dioxide (SO2), nitrogen oxides (NOx), PM2.5, inhalable particles (PM10), carbon monoxide (CO), ammonia (NH3), and volatile organic compounds (VOCs) in GD from 2006 to 2015 were first examined using a dynamic methodology, taking into account economic development, technology penetration, and emission controls. The relative change rates of anthropogenic emissions in GD during 2006–2015 are −48 % for SO2, −0.5 % for NOx, −16 % for PM2.5, −22 % for PM10, 13 % for CO, 3 % for NH3, and 13 % for VOCs. The declines of SO2, NOx, PM2.5, and PM10 emissions in the whole province mainly resulted from the stringent emission control in the Pearl River delta (PRD) region, where most previous control measures were focused, especially on power plants (SO2 and NOx), industrial combustion (SO2, PM2.5, PM10), on-road mobile sources (NOx), and dust sources (PM2.5 and PM10). Emissions from other areas (non-PRD, NPRD), nevertheless, remain relatively stable due to the lax control measures and rapidly growing energy consumption. In addition, emission leaks of SO2 and NOx from industries are observed from PRD to NPRD in 2010 and 2011. As a result, emissions in NPRD are increasingly important in GD, particularly those from industrial combustion. The contribution of NPRD to the total SO2 emissions in GD, for example, increased from 27 % in 2006 to 48 % in 2015. On-road mobile sources and solvent use are the two key sources that should receive more effective control measures in GD. Current control-driven emission reductions from on-road mobile sources are neutralized by the substantial growth of the vehicle population, while VOC emissions in GD steadily increase due to the growth of solvent use and the absence of effective control measures. Besides, future work could focus on power plants and industrial combustion in GD and industrial process sources in NPRD, which still have large emission reduction potentials. The historical emission inventory developed in this study not only helps to understand the emission evolution in GD, but also provides robust data to quantify the impact of emission and meteorology variations on air quality and unveil the primary cause of significant air-quality change in GD in the recent decade.