Filterable PM2.5 concentrations and their chemical characterizations were analyzed for 67 boilers and 25 indirect furnaces located in the Metropolitan Area of Costa Rica from February 2014 to November 2015. The PM2.5 samples were characterized by their composition, focusing on trace elements, inorganic ions and organic and elemental carbon. The results of PM2.5 concentrations ranged from 72 to 735 mgm-3, with the highest concentrations found for sources using biomass fuel, particularly Type B boilers, and the lowest values for diesel boilers. Further speciation of fine particulate matter (PM) showed significant levels of vanadium and nickel for boilers that use heavy fuel oil (bunker); 4886 and 1942 μgm-3, respectively. Copper and manganese were the most relevant metals for biomass burning sources, due to plant absorption from the soil. As for ion concentration, sulfate presented the highest concentrations for biomass boilers and furnaces, whereas chloride only presented the highest concentrations for furnaces. To complete the balance, organic and elemental carbon (OC and EC) analyses were made, in which biomass burning sources presented values five times higher than oil fuels. A Spearman's correlation analysis was made for the data set, revealing significant relationships between heavy metals, sulfate, and fine PM with respect to heavy fuel oil. For the biomass sources, the correlations pointed to K, Na, Mn and, in some cases, oxygen. | Se analizaron las concentraciones filtrables de PM2.5 y sus caracterizaciones químicas para 67 calderas y 25 hornos indirectos ubicados en el Área Metropolitana de Costa Rica desde febrero de 2014 hasta noviembre de 2015. Las muestras de PM2.5 se caracterizaron por su composición, centrándose en oligoelementos, iones inorgánicos y carbono orgánico y elemental. Los resultados de las concentraciones de PM2.5 variaron de 72 a 735 mgm-3, con las concentraciones más altas encontradas para fuentes que utilizan combustible de biomasa, particularmente calderas Tipo B, y el valores más bajos para calderas diesel. Una mayor especiación de partículas finas (PM) mostró una significativa niveles de vanadio y níquel para calderas que utilizan fuel oil pesado (bunker); 4886 y 1942 mgm-3, respectivamente. El cobre y el manganeso fueron los metales más relevantes para las fuentes de combustión de biomasa, debido a Absorción de plantas del suelo. En cuanto a la concentración de iones, el sulfato presentó las mayores concentraciones para calderas y hornos de biomasa, mientras que el cloruro solo presentó las concentraciones más altas para los hornos. Para completar el balance, se realizaron análisis de carbono orgánico y elemental (OC y EC), en los cuales las fuentes de combustión de biomasa presentaron valores cinco veces superiores a los combustibles derivados del petróleo. La correlación de Spearman. Se realizó un análisis para el conjunto de datos, revelando relaciones significativas entre metales pesados, sulfato y PM fino con respecto al fuelóleo pesado. Para las fuentes de biomasa, las correlaciones apuntaron a K, Na, Mn y, en algunos casos, oxígeno. | As concentrações filtráveis ​​de PM2,5 e suas caracterizações químicas foram analisadas para 67 caldeiras e 25 fornos indiretos localizados na Região Metropolitana da Costa Rica de fevereiro de 2014 a novembro de 2015. As amostras de PM2,5 foram caracterizadas por sua composição, com foco em oligoelementos, íons inorgânicos e carbono orgânico e elementar. Os resultados para as concentrações de PM2,5 variaram de 72 a 735 mgm-3, com as concentrações mais altas encontradas para fontes que usam combustível de biomassa, particularmente caldeiras Tipo B, e os valores mais baixos para caldeiras a diesel. A maior especiação de partículas finas (PM) mostrou níveis significativos de vanádio e níquel para caldeiras que usam óleo combustível pesado (bunker); 4886 e 1942 mgm-3, respectivamente. O cobre e o manganês foram os metais mais relevantes para as fontes de combustão da biomassa, devido à absorção das plantas do solo. Em relação à concentração de íons, o sulfato apresentou as maiores concentrações para caldeiras e fornos a biomassa, enquanto o cloreto apresentou as maiores concentrações apenas para os fornos. Para completar o balanço, foram realizadas análises de carbono orgânico e elementar (OC e EC), nas quais as fontes de combustão de biomassa apresentaram valores cinco vezes maiores que os combustíveis derivados do petróleo. A correlação de Spearman. Uma análise foi realizada para o conjunto de dados, revelando relações significativas entre metais pesados, sulfato e MP fino em relação ao óleo combustível pesado. Para fontes de biomassa, as correlações apontaram para K, Na, Mn e, em alguns casos, oxigênio. | Universidad Nacional, Costa Rica | Universidad Autónoma Metropolitana, México | Escuela de Ciencias Ambientales

There is currently great interest in replacing fossil-oil with renewable fuels in energy production. Fast pyrolysis bio-oil (FPBO) made of lignocellulosic biomass is one such alternative to replace fossil oil, such as heavy fuel oil (HFO), in energy boilers. However, it is not known how this fuel change will alter the quantity and quality of emissions affecting human health. In this work, particulate emissions from a real-scale commercially operated FPBO boiler plant are characterized, including extensive physico-chemical and toxicological analyses. These are then compared to emission characteristics of heavy fuel-oil and wood fired boilers. Finally, the effects of the fuel choice on the emissions, their potential health effects and the requirements for flue gas cleaning in small-to medium-sized boiler units are discussed.The total suspended particulate matter and fine particulate matter (PM₁) concentrations in FPBO boiler flue gases before filtration were higher than in HFO boilers and lower or on a level similar to wood-fired grate boilers. FPBO particles consisted mainly of ash species and contained less polycyclic aromatic hydrocarbons (PAH) and heavy metals than had previously been measured from HFO combustion. This feature was clearly reflected in the toxicological properties of FPBO particle emissions, which showed less acute toxicity effects on the cell line than HFO combustion particles. The electrostatic precipitator used in the boiler plant efficiently removed flue gas particles of all sizes. Only minor differences in the toxicological properties of particles upstream and downstream of the electrostatic precipitator were observed, when the same particulate mass from both situations was given to the cells.

Five different domestic heating boilers (automatic, over-fire, with down-draft combustion and gasification) and three types of fuel (lignite, wood and mixed fuel) were examined in 25 combustion tests and correlated with the emissions of particulate matter (PM), carbon monoxide (CO), total organic carbon (TOC) and 12 polycyclic aromatic hydrocarbons (PAHs with MW = 178–278 g/mol) focusing on particle phase. However, the distribution of 12 PAHs in gas phase was considered as well due to the presence mainly of lighter PAHs in gas phase. The PAHs, as well as the CO and TOC, are the indicators of incomplete combustion, and in this study PAH emission increased significantly with increasing emissions of CO and TOC. The PAHs were mainly detected on PM2.5, their contents were increasing linearly with increasing PM2.5 emissions. The highest emission factors of PAHs were measured for boilers of old construction, such as over-fire boiler (5.8–929 mg/kg) and boiler with down-draft combustion (3.1–54.1 mg/kg). Modern types of boilers produced much lower emissions of PAHs, in particular, automatic boiler (0.3–3.3 mg/kg) and gasification boilers (0.2–6.7 mg/kg). In general, the inefficient combustion at reduced output of boilers generated 1.4–17.7 times more emissions of PAHs than the combustion at nominal output of boilers. It is recommended to operate boilers at nominal output with sufficient air supply and to use the proper fuel to minimise PAHs emissions from domestic heating appliances.

The total volume of the coal processing wastes (filter cakes) produced by Russia, China, and India is as high as dozens of millions of tons per year. The concentrations of CO and CO₂ in the emissions from the combustion of filter cakes have been measured directly for the first time. They are the biggest volume of coal processing wastes. There have been many discussions about using these wastes as primary or secondary components of coal-water slurries (CWS) and coal-water slurries containing petrochemicals (CWSP). Boilers have already been operationally tested in Russia for the combustion of CWSP based on filter cakes. In this work, the concentrations of hazardous emissions have been measured at temperatures ranging from 500 to 1000°С. The produced CO and CO₂ concentrations are shown to be practically constant at high temperatures (over 900°С) for all the coal processing wastes under study. Experiments have shown the feasibility to lowering the combustion temperatures of coal processing wastes down to 750–850°С. This provides sustainable combustion and reduces the CO and CO₂ emissions 1.2–1.7 times. These relatively low temperatures ensure satisfactory environmental and energy performance of combustion. Using CWS and CWSP instead of conventional solid fuels significantly reduces NOₓ and SOₓ emissions but leaves CO and CO₂ emissions practically at the same level as coal powder combustion. Therefore, the environmentally friendly future (in terms of all the main atmospheric emissions: CO, CO₂, NOₓ, and SOₓ) of both CWS and CWSP technologies relies on low-temperature combustion.

Burning coal for winter heating has been considered a major contributor to northern China's winter haze, with the district heating boilers holding the balance. However a decade of intensive efforts on district heating boilers brought few improvements to northern China's winter air quality, arousing a speculation that the household heating stoves mainly in rural area rather than the district heating boilers mainly in urban area dominate coal emissions in winter. This implies an extreme underestimation of rural household coal consumption by the China Energy Statistical Yearbooks (CESYs), although direct evidence supporting this speculation is lacking. A village energy survey campaign was launched to gather the firsthand information on household coal consumption in the rural areas of two cities, Baoding (in Hebei province) and Beijing (the capital of China). The survey data show that the rural raw coal consumption in Baoding (5.04 × 103 kt) was approximately 6.5 times the value listed in the official CESY 2013 and exceeded the rural total of whole Hebei Province (4668 kt), revealing a huge amount of raw coal missing from the current statistical system. More importantly, rural emissions of particulate matter (PM) and SO2 from raw coal, which had never been included in widely distributing environmental statistical reports, were found higher than those from industrial and urban household sectors in the two cities in 2013, which highlights the importance of rural coal burning in creating northern China's heavy haze and helps to explain why a number of modeling predictions on ambient pollutant concentrations based on normal emission inventories were more bias-prone in winter season than in other seasons. We therefore recommend placing greater emphasis on the “missing” rural raw coal to help China in its long-term ambition to achieve clean air in the context of rapid economic development.

Coal burning in power plants and industrial boilers is the largest combustion source of mercury emissions in China. Together, power plants and industrial boilers emit around 250 tonnes of mercury each year, or around half of atmospheric mercury emissions from anthropogenic sources in the country. Power plants in China are generally equipped with multi-pollutant control technologies, which offer the co-benefit of mercury removal, while mercury-specific control technologies have been installed in some facilities. In contrast, most industrial boilers have only basic or no flue gas cleaning. A combination of measures, including energy conservation, coal switching and blending, reducing the mercury contents of coals through washing, combustion controls, and flue gas cleaning, can be used to reduce mercury emissions from these stationary combustion sources. More stringent emission standards for the major air pollutants from coal-fired power plants and industrial boiler, along with standards for the previously unregulated mercury, were implemented recently, which is expected to bring significant reduction in their mercury emissions through the necessary upgrades of multi-pollutant and mercury-specific control technologies. Meanwhile, strong monitoring capacity and strict enforcement are necessary to ensure that the combustion sources operate in compliance with the new emission standards and achieve significant reduction in the emissions of mercury and other air pollutants.

This study analyzed the profiles of polycyclic aromatic hydrocarbons (PAHs) in filterable PM2.5 particles collected from a total of 71 boilers and 22 indirect type furnaces that burn liquid and biomass fuels in the Metropolitan Area of Costa Rica, from February 2014 to November 2015. Modified method NIOSH 5506 was used to analyze PAHs content present in the filter samples. The average concentration of PM2.5 showed values between 18 and 735 mg m−3, based on the source and fuel type used, while the total PAHs in the PM2.5 fraction ranged 1.02–592 μgm−3. For biomass boilers, the most abundant species were Benzo[g,h,i]perylene (BghiP) (35.7–46.5%), Indeno[1,2,3-cd]pyrene (IND) (20.6–27.1%), Benzo[a]pyrene (BaP) (5.2–14.7%) and Dibenzo[a,h]anthracene (DBA) (3.2–13.9%), while for liquid fuels IND (12.8–20.5%), BghiP (7.9–21.2%), Fluoranthene (Flu) (14.5–21.3%) and Pyrene (Pyr) (9.8–14.5%) prevailed. The particles from biomass furnace emissions present higher concentrations of PAHs classified by the U.S. EPA as probable human carcinogens causing a greater health risk than other fuels. Among the diagnostic concentration ratios examined, only BaP/(BaP+Chr), BaA/Chr, BaA/BaP and Pyr/BaP coefficients demonstrated codependency on the type of fuel used.

A mathematical model was developed to simulate the oxidation of total sulfite in the holding tank of ammonia-based flue gas desulfurization (FGD) system. The model could provide predictions of the oxidation ratio of total sulfite at different operating condition such as pH, concentration of total sulfur, air flow and residence time. The calculation results of an ammonia-based FGD system for 2 × 150 MW boilers by this model were compared to that of corresponding measured values. The comparison results show that the simulated oxidation ratio of total sulfite agrees well with the measured data. The difference between calculated values and measured data is below 4.2%. This model appears to be beneficial for optimizing design and operation of total sulfite oxidation of an ammonia-based FGD system.

The residue concentrations and congener profiles of polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) were examined in fly ash and bottom ash released from different thermal industrial processes in Vietnam. PCDD/F concentrations and toxic equivalents (TEQs) in the ash samples varied greatly and decreased in the following order: steel making > aluminum recycling > medical waste incinerator > boilers > municipal waste incinerator > tin production > brick production > coal-fired power plant. Both the precursor and de novo synthesis were estimated as possible formation mechanisms of dioxins in the ash, but the latter pathway was more prevalent. The highest emission factors were estimated for the ash released from some steel-making plants, aluminum-recycling facilities, and a medical waste incinerator. The emission factors of PCDD/Fs in ash released from some steel plants of this study were two to six times higher than the UNEP Toolkit default value. The annual emission amount of ash-bound dioxins produced by 15 facilities in our study was estimated to be 26.2 to 28.4 g TEQ year⁻¹, which mainly contributed by 3 steel plants. Health risk related to the dioxin-containing ash was evaluated for workers at the studied facilities, indicating acceptable risk levels for almost all individuals. More comprehensive studies on the occurrence and impacts of dioxins in waste streams from incineration and industrial processes and receiving environments should be conducted, in order to promote effective waste management and health protection scheme for dioxins and related compounds in this rapidly industrializing country.

Large amounts of air pollutants emitted from massive coal combustion result in the air quality deterioration and threaten public health in China. To improve air quality, the Chinese government released the coal cap policy to reduce coal consumption. So it is important and necessary to understand the possible environmental impact and relevant health benefits from the coal cap policy. The purpose of this paper is to quantify the air quality improvement and to evaluate the health benefits from the implementation of the coal cap policy, with the Beijing–Tianjin–Hebei (BTH) region as the study area. The results showed that the emissions of SO₂, NOx, CO, VOCs, PM₁₀, and PM₂.₅ could be reduced by 20–40% in the BTH region in 2020 and all pollutants from industrial boilers notably decreased. Under the coal cap policy, the PM₂.₅ concentration in the whole region would fall by 11.27%, and the total economic benefit from health impacts could achieve 26.61 (13.29 to 39.14) billion RMB (3.9 billion USD) in the BTH region in 2020, accounting for 0.43% (0.21 to 0.63%) of regional GDP in 2013. This study demonstrated the quantification of environmental effect and health benefit from the coal cap policy, which could be used for the complete cost–benefit analysis and provide the sufficient support for policy makers to implement the coal cap policy in the BTH region and other areas of China.