The impact assessment of Diwali fireworks emissions on the air quality of a tropical urban site, Hyderabad, India, during three consecutive years

Diwali is one of the largest festivals for Hindu religion which falls in the period October–November every year. During the festival days, extensive burning of firecrackers takes place, especially in the evening hours, constituting a significant source of aerosols, black carbon (BC), organics, and trace gases. The widespread use of sparklers was found to be associated with short-term air quality degradation events. The present study focuses on the influence of Diwali fireworks emissions on surface ozone (O₃), nitrogen oxides (NO _x ), and BC aerosol concentration over the tropical urban region of Hyderabad, India during three consecutive years (2009–2011). The trace gases are analyzed for pre-Diwali, Diwali, and post-Diwali days in order to reveal the festivity’s contribution to the ambient air quality over the city. A twofold to threefold increase is observed in O₃, NO _x , and BC concentrations during the festival period compared to control days for 2009–2011, which is mainly attributed to firecrackers burning. The high correlation coefficient (~0.74) between NO _x and SO₂ concentrations and higher SO₂/NO _x (S/N) index suggested air quality degradation due to firecrackers burning. Furthermore, the Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observation-derived aerosol subtyping map also confirmed the presence of smoke aerosols emitted from firecrackers burning over the region. Nevertheless, the concentration level of pollutants exhibited substantial decline over the region during the years 2010 and 2011 compared to 2009 ascribed to various awareness campaigns and increased cost of firecrackers.     

Attribution of aerosol light absorption to black carbon and volatile aerosols

We investigated the contribution of volatile aerosols in light-absorption measurement by three filter-based optical instruments [aethalometer, continuous light-absorption photometer (CLAP), and continuous soot monitoring system (COSMOS)] at Gosan Climate Observatory (GCO) from February to June 2012. The aerosol absorption coefficient (σ _abs) and the equivalent black carbon (BC) mass concentration (M _BC) measured by the aethalometer and CLAP showed good agreement with a difference of 9 %, which is likely due to the instrumental uncertainty. However, σ _abs and M _BC measured by the COSMOS with a heated inlet were found to be approximately 44 and 49 % lower than those measured by the aethalometer and CLAP under ambient conditions, respectively. This difference can be attributed to the light absorption by the volatile aerosols coexisting with the BC. Even considering inherent observational uncertainty, it suggests that approximately 35–40 % difference in the σ _abs and M _BC can be contributed by volatile aerosols. Increase in the difference of M _BC measured by the aethalometer and COSMOS with the increasing thermal organic carbon (OC) measured by Sunset OC/EC analyzer further suggests that the filter-based optical instruments without the use of a heater are likely to enhance the value of σ _abs and M _BC, because this sample air may contain both BC and volatile aerosols.     

The impact of ground-level fireworks (13?km long) display on the air quality during the traditional Yanshui Lantern Festival in Taiwan

In this study, the concentrations of CO, non-methane hydrocarbons, NO_X, SO₂, benzene, toluene, ethylbenzene, xylene (BTEX), PM₁₀, and PM_2.5 were continuously monitored before and after the fireworks display during the traditional Lantern Festival from March 2?C7, 2007 in Yanshui Town, Taiwan. Major roads in Yanshui Town were surrounded by fireworks 13 km in length, with the display lasting for 45 min. More than 200 small firecracker towers popped up randomly in town, resulting in exceedingly inhomogeneous air quality until the end of display at 03:00 the next day, March 5. During the fireworks display, the hourly concentration of PM₁₀ and PM_2.5 at Yanshui Primary School reached about 429 and 250 ??g m^???3, respectively, which is 10 times the normal level, and 6 s values even went as high as 1,046 and 842 ??g m^???3, respectively. Similarly, BTEX concentration went up to about five to 10 times its normal value during the fireworks display. As indicated by the distribution of submicron particle sizes, the number of particles with a diameter less than 100 nm increased abruptly during the event period. Metal components with concentrations of more than 10 times higher than the normal value at Yanshui Primary School were Sr, K, Ba, Pb, Al, Mg, and Cu, in sequence. Among water-soluble ions, the content of K^?+?, Mg^2?+?, and Cl^??? increased the most, all of which were related to the materials used in the fireworks. The results of this study indicate that fireworks can cause an abrupt increase in the concentration of trace substances in the air within a short period. Although the risks of these trace substances on public health remain to be further assessed, the study results can be utilized in the management of folk events.     

烟花爆竹禁燃对春节期间东北地区空气质量影响评估

利用2015—2017年春节期间东北地区主要大气污染物(PM_(10)、PM_(2.5)、SO_2、NO_2、CO和O3)质量浓度监测资料及相应气象因子(温度、湿度、风速和气压)观测资料,分析了春节期间烟花爆竹禁燃对东北地区空气质量的影响。结果表明:随着东北地区主要城市禁燃力度的增强,空气质量逐年提升,PM_(2.5)和SO_2浓度逐年大幅度下降。禁燃可明显降低城区PM_(2.5)浓度,而由于春节期间污染源整体减少,城区和城郊监测点PM_(2.5)浓度值差异减小。烟花爆竹对PM_(10)和PM_(2.5)浓度影响高于对气体污染物SO_2、NO_2和CO的影响。此外,气象条件对东北地区春节期间禁燃改善空气质量的效果也有明显影响。因此,结合春节期间的气象条件,在东北地区实施禁燃政策动态调整非常必要。     

Study of temporal variation in ambient air quality during Diwali festival in India

The variation in air quality was assessed from the ambient concentrations of various air pollutants [total suspended particle (TSP), particulate matter ≤10 μm (PM₁₀), SO₂, and NO₂] for pre-Diwali, Diwali festival, post-Diwali, and foggy day (October, November, and December), Delhi (India), from 2002 to 2007. The extensive use of fireworks was found to be related to short-term variation in air quality. During the festival, TSP is almost of the same order as compared to the concentration at an industrial site in Delhi in all the years. However, the concentrations of PM₁₀, SO₂, and NO₂ increased two to six times during the Diwali period when compared to the data reported for an industrial site. Similar trend was observed when the concentrations of pollutants were compared with values obtained for a typical foggy day each year in December. The levels of these pollutants observed during Diwali were found to be higher due to adverse meteorological conditions, i.e., decrease in 24 h average mixing height, temperature, and wind speed. The trend analysis shows that TSP, PM₁₀, NO₂, and SO₂ concentration increased just before Diwali and reached to a maximum concentration on the day of the festival. The values gradually decreased after the festival. On Diwali day, 24-h values for TSP and PM₁₀ in all the years from 2002 to 2007 and for NO₂ in 2004 and 2007 were found to be higher than prescribed limits of National Ambient Air Quality Standards and exceptionally high (3.6 times) for PM₁₀ in 2007. These results indicate that fireworks during the Diwali festival affected the ambient air quality adversely due to emission and accumulation of TSP, PM₁₀, SO₂, and NO_2.     

Comparison of elemental and black carbon measurements during normal and heavy haze periods: implications for research

Studies specifically addressing the elemental carbon (EC)/black carbon (BC) relationship during the transition from clean-normal (CN) air quality to heavy haze (HH) are rare but have important health and climate implications. The present study, in which EC levels are measured using a thermal-optical method and BC levels are measured using an optical method (aethalometer), provides a preliminary insight into this issue. The average daily EC concentration was 3.08?±?1.10 μg/m³ during the CN stage but climbed to 11.77?±?2.01 μg/m³ during the HH stage. More importantly, the BC/EC ratio averaged 0.92?±?0.14 during the CN state and increased to 1.88?±?0.30 during the HH state. This significant increase in BC/EC ratio has been confirmed to result partially from an increase in the in situ light absorption efficiency (σ _ap) due to an enhanced internal mixing of the EC with other species. However, the exact enhancement of σ _ap was unavailable because our monitoring scheme could not acquire the in situ absorption (b _ap) essential for σ _ap calculation. This reveals a need to perform simultaneous measurement of EC and b _ap over a time period that includes both the CN and HH stages. In addition, the sensitivity of EC to both anthropogenic emissions and HH conditions implies a need to systematically study how to include EC complex (EC concentration, OC/EC ratio, and σ _ap) as an indicator in air quality observations, in alert systems that assess air quality, and in the governance of emissions and human behaviors.     

Characterization of ambient black carbon and wood burning particles in two urban areas

Previously it has been suggested that certain organic aerosol components of wood smoke have enhanced ultraviolet absorption at 370 nm relative to 880 nm in two-wavelength aethalometer measurements. This enhanced absorption could serve as an indicator of wood burning particles. Two-wavelength (370 nm and 880 nm) aethalometer measurements were made at urban sites in Rochester, New York and Laredo, Texas from August 1 to December 31, 2009 and from December 23, 2007 to January 2, 2008, respectively. In Rochester, Delta-C (UVBC(370 nm)- BC(880 nm)) values were higher by a factor of 3 during the night than during the day in November and December when residential wood burning was common. In Laredo, particularly high Delta-C values were observed on Christmas Eve and New Year's Eve and were attributed to biomass burning and firework emissions. Exponential decay was found to be a good estimator for predicting BC concentrations at different wind speeds regardless of wind directions.     

烟花爆竹燃放对四川盆地边缘城市环境空气的影响及其污染传输特征研究

为了解四川盆地边缘城市环境空气质量受烟花爆竹燃放影响的特征,选取位于成都平原西南部的乐山市进行研究。研究发现,春节期间乐山市受烟花爆竹燃放影响的环境空气中的颗粒物及其组分的浓度变化趋势一致。相关性分析结果显示：在除夕夜烟花爆竹燃放影响时间段内,乐山市环境空气中的颗粒物(PM₁₀、PM_2.5)浓度与SO₄^2-、F^-、Al、K、Mn、Cu、Zn等组分浓度呈显著正相关,Pearson相关系数达到了0.48～0.73;Al、Si、K、Mn、Cu、Zn等组分浓度之间也表现出显著正相关,Pearson相关系数高达0.78～0.98。其中,K⁺浓度占比从0%上升到7.32%,SO₄^2-浓度占比从18.94%上升到24.73%,Cl^-浓度占比从0.46%上升到4.29%,Cu元素浓度占比从0.05%上升到0.30%,Al元素浓度占比从5.87%上升到7.46%。除夕夜烟花爆竹燃放影响期间,乐山市中部和北部区...     

Diurnal concentrations variations,size distributions for ambient air particles and metallic pollutants (Cr,Mn, Ni,Cd, Pb) during summer season at a traffic area

This study characterized and discussed particulate ambient air particulate concentrations and seasonal variations for PM₁₈, PM₁₀, PM_2.5, and PM₁ during June 2013–July 2013 at this traffic sampling site. In addition, this study also characterized the ambient air particulates size distributions by using MOUDI-100S4 sampler to collect 1-day the ambient suspended particles (PM₁₈, PM₁₀, PM_2.5, and PM₁) at this sampling site. In addition, the study also showed that the main pollutants contributions were from traffic and residual areas. As for the pollutants seasonal concentrations variations, the results indicated that the average particle concentrations orders were all displayed as daytime?>?nighttime for PM₁₈, PM₁₀, PM_2.5 and PM₁ at this characteristic sampling site. The results further indicated that the mean highest of metal concentrations in this study indicated that the average metal concentration were all displayed as Mn?>?Cr?>?Ni?>?Pb?>?Cd for PM₁₈, PM₁₀, PM_2.5 and PM₁ on daytime and nighttime at this characteristic sampling site.     

Monitoring and dispersion modelling of emissions from the fluidised bed combustion of poultry litter

Gaseous emissions from the fluidised bed combustion of chickenlitter were monitored and recorded. Emission data was used tocreate a dispersion model for a proposed site on a poultry farmin Limerick, Ireland. Variables within the combustion unit notonly influenced combustion but also emission levels ofpollutants such as SO₂ and NO_x. CO emissions decreased withuse of the correct ratio between fluidising and secondary air,the staging of secondary air and the degree of turbulence withwhich the secondary air is introduced. Dispersion modelling ofactual combustion at a proposed poultry unit predicted thatground level concentrations for the set of emissions data wouldbe below the limits and guidelines set by air quality standards.This was true for both and line source. Line sourceconcentration levels were less than those for point source.     

Dust events and their influence on aerosol optical properties over Jaipur in Northwestern India

In this study, we systematically document the link between dust episodes and local scale regional aerosol optical properties over Jaipur located in the vicinity of Thar Desert in the northwestern state of Rajasthan. The seasonal variation of AOT_{500 nm} (aerosol optical thickness) shows high values (0.51?±?0.18) during pre-monsoon (dust dominant) season while low values (0.36?±?0.14) are exhibited during winter. The Ångström wavelength exponent has been found to exhibit low value (<0.25) indicating relative dominance of coarse-mode particles during pre-monsoon season. The AOT increased from 0.36 (April_mean) to 0.575 (May–June_mean). Consequently, volume concentration range increases from April through May–June followed by a sharp decline in July during the first active phase of the monsoon. Significantly high dust storms were observed over Jaipur as indicated by high values of single scattering albedo (SSA_{440 nm}?=?0.89, SSA_{675 nm}?=?0.95, SSA_{870 nm}?=?0.97, SSA_{1,020 nm}?=?0.976) than the previously reported values over IGP region sites. The larger SSA values (more scattering aerosol), especially at longer wavelengths, is due to the abundant dust loading, and is attributed to the measurement site’s proximity to the Thar Desert. The mean and standard deviation in SSA and asymmetry parameter during pre-monsoon season over Jaipur is 0.938?±?0.023 and 0.712?±?0.017 at 675 nm wavelength, respectively. Back-trajectory air mass simulations suggest Thar Desert in northwestern India as the primary source of high aerosols dust loading over Jaipur region as well as contribution by long-range transport from the Arabian Peninsula and Middle East gulf regions, during pre-monsoon season.     

Motor Vehicle Contributions to Ambient PM10 and PM2.5 at Selected Urban Areas in the USA

A source apportionment study was carried out to estimate the contribution of motor vehicles to ambient particulate matter (PM) in selected urban areas in the USA. Measurements were performed at seven locations during the period September 7, 2000 through March 9, 2001. Measurements included integrated PM_2.5 and PM₁₀ concentrations and polycyclic aromatic hydrocarbons (PAHs). Ambient PM_2.5 and PM₁₀ were apportioned to their local sources using the chemical mass balance (CMB) receptor model and compared with results obtained using scanning electron microscopy (SEM). Results indicate that PM_2.5 components were mainly from combustion sources, including motor vehicles, and secondary species (nitrates and sulfates). PM₁₀ consisted mainly of geological material, in addition to emissions from combustion sources. The fractional contributions of motor vehicles to ambient PM were estimated to be in the range from 20 to 76% and from 35 to 92% for PM_2.5 and PM₁₀, respectively.     

工业链条炉燃用型煤与原煤颗粒物排放特征

选取燃烧型煤和原煤的典型链条炉,应用自行设计的固定源烟气颗粒物稀释采样系统,现场测试细颗粒物PM_(2.5)、PM_(10)和金属元素的排放特征。结果表明,型煤燃烧细颗粒物的排放比例高于原煤,型煤燃烧除尘器进口、出口PM_(2.5)质量比原煤燃烧分别增加715%和708%。燃烧型煤时,As和Pb在各粒径段的质量比均比原煤大。同时,由于型煤燃烧可吸入颗粒物的排放比例增加,包含或附着在烟尘上的金属元素排放比例也相应增加。     

Phenanthrene sorption to humic acids, humin, and black carbon in sediments from typical water systems in China

Humic acid (HA) and humin (HM) were extracted with 0.1 M NaOH and black carbon (BC) was isolated using a combustion method at 375°C from six sediments in different areas in China and their sorption isotherms for phenanthrene (Phen) were determined. All sorption isotherms were nonlinear and fitted well with the Freundlich model. Among the SOM, HM and BC with more aromatic carbon controlled the sorption nonlinearity and capacity. Compared to HM, higher K _oc values were observed for BC due to the combustion of organic matter and native sorbates in HM. For HAs isotherms, a positive relation was observed between the K _oc values and aliphaticity or H/C ratios, but a negative relation was shown between the n values and polarity of HAs. HA, HM, and BC were responsible for 0.4–9.3%, 46–97%, and 65–96% of the total sorption, respectively, indicating the dominance of HM and BC fractions in overall sorption of Phen by the sediments.     

Air Pollution Concentrations of PM2.5, PM10 and NO2 at Ambient and Kerbsite and Their Correlation in Metro City – Mumbai

Ambient concentrations of PM_2.5 and PM₁₀ are of concern with respect to effects on human health and environment. Increased levels of mortality and morbidity have been associated with respirable particulate air pollution. In India, it is not yet mandatory to monitor PM_2.5 levels therefore very limited information is available on PM_2.5 levels. To understand the fine particle pollution and also correlate with PM₁₀ which are monitored regularly in compliance with ambient air quality standards. This study was carried out to monitor PM_2.5, PM₁₀, and NO₂ for about one year in a residential cum commercial area of Mumbai city with a view to understand their correlation. The average PM_2.5 concentration at ambient and Kerbsite was 43 and 69 μg/m³. The correlation coefficients between PM_2.5 and PM₁₀ at ambient and Kerbsite were 0.83 and 0.85 respectively thus indicating that most of the PM_2.5 and PM₁₀ are from similar sources. TSP, PM₁₀ levels exceeded Central Pollution Control Board(CPCB) standard during winter season. PM_2.5 levels also exceeded 24 hourly average USEPA standard during winter season indicating unhealthy air quality.     

哈大绥城市“十三五”期间大气环境容量分析

根据2016—2020年哈尔滨市、大庆市、绥化市(以下称哈大绥)国控环境空气自动监测站的SO₂、NO₂、PM_2.5监测资料,统计年鉴中行政区划、污染物排放及气象等监测数据,分析哈大绥区域环境空气质量的变化趋势和测算因子,采用A值法核定了哈大绥区域SO₂、NO₂、PM_2.5的大气环境容量。结果表明:哈大绥SO₂、NO₂、PM_2.5 3项污染物采暖季的大气环境容量均呈逐年递增趋势。通过计算环境承载能力发现,哈大绥SO₂、NO₂、PM_2.5 3项污染物在非采暖季均具有高承载能力,哈大绥非采暖季环境容量高于采暖季。哈尔滨的个别污染物仍然处于临界超载状态,为减少重污染天气,应进一步削减采暖季污染物排放量。     

Study on concentration of ambient NH 3 and interactions with some other ambient trace gases

We present diurnal variation of ambient ammonia (NH₃) in relation with other trace gases (O₃, CO, NO, NO₂, and SO₂) and meteorological parameters at an urban site of Delhi during winter period. For the first time, ambient ammonia (NH₃) was monitored very precisely and continuously using ammonia analyzer, which operates on chemiluminescence method. NH₃ estimation efficiency of the chemiluminescence method (>90%) is much higher than the conventional chemical trapping method (reproducibility 4.5%). Ambient NH₃ concentration reaches its maxima (46.17 ppb) at night and minimum during midday. Result reveals that the ambient ammonia (NH₃) concentration is positively correlated with ambient NO (r ²?=?0.79) and NO₂ (r ²?=?0.91) mixing ratio and negatively correlated with ambient temperature (r ²?=???0.32). Wind direction and wind speed indicates that the nearby (~500 m NW) agricultural fields may be major source of ambient NH₃ at the observational site.     

Profiling and monitoring of DOM in brewery wastewater and treated wastewater

Dissolved organic matter (DOM) in raw and treated wastewater from two breweries in Thailand was profiled and monitored for the purpose of water reclamation. The wastewater and the effluent from the use of an upflow anaerobic sludge blanket (UASB) and activated sludge (AS) were collected and analyzed through a resin fractionation method using the fluorescent excitation?Cemission matrix (FEEM) technique. The results revealed that the major organic fractions in the brewery wastewater were hydrophobic acid (HPOA) and hydrophilic base (HPIB), accounting for 65% of total dissolved organic carbon (DOC) mass for brewery A and 56% of total DOC mass for brewery B. The FEEM results indicated that the organic matter in the wastewaters of both breweries were mainly composed of tryptophan-like substances, represented by peaks C (230 nm_Ex/340?C365 nm_Em) and D (265?C295 nm_Ex/315?C390 nm_Em), and humic-like substances, represented by peaks E (290 nm_Ex/400 nm_Em), F (330?C335 nm_Ex/395?C410 nm_Em), and G (255?C265 nm_Ex/435?C455 nm_Em). The analysis revealed that the reduction of DOM occurred mostly during the UASB treatment where most of the DOM reduction resulted from the removal of the HPOA and HPIB fractions. The HPOA fraction, a group of humic-like substances, is of particular concern when reclaiming treated brewery wastewater, and although it was reduced by more than 80% of its initial amount, it was still a dominant DOM fraction in the effluents.     

Variation in spatial pattern of criteria air pollutants before and during initial rain of monsoon

Spatial patterns of various criteria air pollutants,like SO₂, NO₂, O₃, and TSP were studied atShahdara National Ambient Air Quality Monitoring stationin Delhi (India) in July 1999. The minimum pollutantconcentrations were observed during morning hours,whereas the highest concentrations were found during thelate night hours, which seem to be related with thevehicular emission. Pre-monsoon daily ambient airquality spatial pattern was compared with the spatialpattern during initial and subsequent rain shower ofmonsoon. These spatial patterns were found to beessentially the same before and during rain, however asignificant decrease in SO₂, NO₂ and TSPconcentrations (40-45%) was observed after initial andsubsequent rains of the monsoon, demonstrating theimportance of rainfall in the scavenging of thesecriteria air pollutants.     

杭州城区环境空气中二口恶英浓度状况研究

依据2009年7月至2012年2月连续3年对杭州城区环境空气中二英（PCDD/Fs）采样分析结果得知,杭州城区环境空气中二英毒性当量质量浓度变化范围为0.13～0.55 pg TEQ/m³,均值为0.34 pg TEQ/m³。城区环境空气中二英浓度季节变化不显著,夏季略低于冬季;城区范围内不同功能区之间二英浓度差别不显著;连续3年监测结果未显现二英年度变化趋势。沙尘暴天气环境空气中二英浓度显著增高,日常天气和烟花爆竹集中燃放天气环境空气中二英形态分布存在明显区别,烟花爆竹集中燃放期间八氯代二苯并-对-二英（OCDD）占总质量浓度比例显著提高。利用IBM SPSS Statistics 19.0统计软件对24个监测结果聚类分析发现,杭州城区环境空气中二英的同类物分布具有明显的“源”分布特征。