The huge amount of petroleum hydrocarbons contaminated sites is the heritage of a long history of fossil fuels usage. Reducing petroleum hydrocarbons levels in contaminated soils by Fenton reaction and with the aid of one or two agents such as solvents, surfactants, or vegetable oils has been studied in recent years, with successful reported results. Nonetheless, destruction of the aliphatic fraction of total petroleum hydrocarbon (TPH) by Fenton reaction has been studied to a lesser extent as compared to the aromatic fraction of TPH. Additionally, studies regarding the effect of humic acid (HA) on Fenton reaction reported contradictory results, and more research is necessary to clarify HA effects. Lastly, although achieving the highest efficiency is the main objective of soil remediation technologies, the environmental side effects of the applied processes should be considered as important as the efficiency. In light of these, the main aim of this project was to increase Fenton treatment efficiency by using an environmental friendly solvent, ethyl lactate (EL). The project objectives included determining optimum levels for the reagents of Fenton reaction and desorption process such as hydrogen peroxide (H2O2) and EL, identifying the kinetic of TPH desorption and destruction of petroleum hydrocarbons by Fenton reaction in addition to analysing the effects of EL on these processes. Through desorption tests, EL/water solution demonstrated great ability to increase the removal efficiency and desorption of sorbed TPH. Desorption by EL/water solution consisted of a very fast desorption stage followed by a slow stage. After 30 min of desorption, the removal efficiency of TPH increased from 63% to 81% for EL=25% and EL=100%, respectively. The initial desorption rate for 25% and 100% were 1.625 mg/min and 3.368 mg/min, respectively. The results of batch experiments indicated that EL%=10% was the optimum value for the EL-modified Fenton reaction. After 4 h, an increase in H2O2 concentration from 0.1 M to 2 M at L/S=2 and EL=25% increased the removal efficiency of TPH from 68.41% to 90.21%. HA addition up to 150 mg/l was also studied. For fraction 1, adding HA led to an increase in removal efficiency while for fraction 2, only HA=150mg/l had higher removal efficiency than the HA=0 case and for fraction 3, addition of HA in the studied range could not increase the removal efficiency. A good compatibility of zero-valent iron nanomaterial with H2O2 was proved. Laboratory column experiments were finally carried out to remove petroleum hydrocarbons from diesel-contaminated soil with EL to reproduce the conditions of in-situ treatment. The remaining diesel in soil decreased by increasing H2O2 molarity from 0.1 M to 0.5 M whereas a further increase to 2 M led to an increase in remaining diesel in soil. The stability of H2O2 in EL has been observed which signifies good potential for in-situ applications. Overall, the project has demonstrated the feasibility of EL-modified Fenton reaction for the remediation of petroleum-contaminated soil.

The debates and discussions (discourses) surrounding shale gas in the United Kingdom (UK) far outstrip any physical development of the potential energy source. The UK sits on a significant potential resource of 1329tcf. (Andrews, 2013) of shale gas, yet there are increasingly polarised positions on whether this resource should be developed. On the one hand, proponents of its development point to the United States (US) and the significant economic impact the rapid expansion of shale gas development has had. On the other, concerns are raised about the purported negative environmental impacts shale gas development may have, particularly questions about its climatic impact and the contamination of water. The polarisation of UK shale gas discourses made it impossible to conceive that proponents of each 'side' were not viewing the same version of shale gas; the differences were simply too great. An alternative research framework is therefore developed within this thesis. An approach which does not impose pre-emptive boundaries on the discourses, with the binary understandings of 'pro' or 'anti' and the thematic categorisation of content being done away with and tossed onto the bonfire. The approach draws on Actor-Network Theory (ANT) which treats shale gas discourses as actor-networks within which the content of discourse, such as water contamination, are considered actors. These actor-networks are traced to explore the form and formation of UK shale gas discourses, and ultimately why some discourses become salient, whilst others fail. Given the disconnect between different positions on shale gas, Mol's (1999 & 2002) work on multiple realities was incorporated to argue that rather than there being multiple perspectives on shale gas, there are rather "more than one, less than many" (Mol, 2002) versions, or realities, of shale gas. This research draws on 83 semi-structured interviews with a variety of stakeholders interested in the emergence of UK shale gas and were conducted between 2013 and 2014. By following these stakeholders as they lay out their realities of shale gas through actor-networks of discourses, this research explores which actors stakeholders mobilise within their discourses, and how they are performed through the alignment and translation of the actors to produce effect - shale gas discourses. This, enabled a nuanced insight into UK shale gas discourses from those mobilising them. In doing so, this research highlighted several key aspects of UK shale gas discourses. First and foremost was the dominance of water discourses. This was due to water contamination as a result of shale gas development being seen as a foregone conclusion by stakeholders, as a result of it becoming a punctualised actor, whereby water contamination was reduced to end effect. The explanations of how or why it may occur being successfully masked within the actor-networks. The research also highlighted the reason for this dominance being in no small part to the spatial aspects of the US experience of shale gas development being imported without spatial-context to the UK. The way stakeholders performed UK shale gas discourses was also a significant finding, specifically that discourses were a system of alliances with multiple actors mobilised in support of a broader discourse, as opposed to a structured thematic consideration of the issues. Finally, the incorporation of multiple realities led to the conclusion that the negativity of shale gas has become a 'matter of fact', with a dominant more-negative reality transcending all others to a lesser or greater-degree and influencing discourses of shale gas with negative translations. Overall, this research speaks to the small but growing literature on UK shale gas discourses. The development and employment of an alternative research framework based on ANT and multiple realities may have wider applications both for exploring UK shale gas discourses in greater depth, but also for considering other controversies.

Carbon capture and storage (CCS) is considered to be one of the strategically important carbon abatement technologies that can be used to effectively reduce the carbon emissions from fossil fuel power plants and other large scale industrial processes, which are the major stationary sources of greenhouse carbon emissions. Compared to other capture technologies, solid adsorbents looping technology (SALT) based post-combustion carbon capture, an alternative to the state-of-the-art energy intensive amine scrubbing process, is widely viewed as being the most viable technology that can be used as either as a retrofit to existing power plants or new build capacity. The potential success of SALT technology is largely determined by the development of novel CO2 adsorbents. Amine immobilized solid adsorbents are highlighted to be used in SALT technology due to their high CO2 selectivity (CO2/N2 >1000), suitable adsorption temperature and tolerance of moisture. Although they have so much advantages on carbon capture, the oxidation and degradation of solid amines are still a significant problem to be overcome. The degradation of the amine adsorbent can lead to a reduction in CO2 capture performance and selectivity, an increase in the process cost and corrosion problems. The aim of this project is to 1) develop new solid adsorbent materials with higher CO2 capture ability and superior adsorption-desorption lifetime performance; 2) to investigate effective measures to minimise or effectively prevent the thermal and oxidative degradation of the sorbent materials; 3) to explore approaches that can rejuvenate the degraded sorbents for re-use or convert them into other value-added products. Firstly, a series of PEI-the porous siliceous cellular foams (SCF) adsorbents have been developed and characterised. The results show a relationship between the textural properties of SCF and CO2 adsorption ability of adsorbents. A highly effective hydrothermal methodology was developed to produce extremely mesoporous silica materials with well-defined mesoporous structures and greatly increased pore volumes of up to 3.2 cm3/g. The PEI adsorbents prepared using SCF-3-120-24 (1.6 cm3/g) was found to have CO2 capture capacities of nearly 180.8 mg/g, which represents the highest adsorption capacity ever reported for supported PEI adsorbents. Secondly, lifetime performance testing and strategies to mitigate the thermal-oxidative degradation of PEI adsorbents and rejuvenation of the degraded PEI was investigated. The presence of moisture and additives was seen to enhance the thermal-oxidative stability of PEI. Furthermore, the doping of Na2B4O7 hydrates can increase the cyclic adsorption-desorption lifetime performance of PEI adsorbent. Meanwhile, the CO2 adsorption capacity of one heavily degraded PEI adsorbent was increased from 2.8 wt% to 6.2 wt% after rejuvenation test. Finally, hydrous pyrolysis and a continuous flow reactor system was used in catalytic hydrotreatments and hydrothermal treatments of six model MEA degradation compounds and two degraded MEA solvents. Most of the model compounds and degraded MEA was converted to piperazine derivatives in a H2 reaction atmosphere and pyrazine derivatives in NH3 reaction atmosphere. Piperazines and pyrazines are a type of important pharmaceutical intermediates.

The work in this thesis focuses on the synthesis of metal organic frameworks (MOFs) both in batch and continuous work. Improvements are made in both, compared to the previous research. Furthermore, post-modification experiments are conducted to advance the characteristics of end product. Also, their application as solid sorbents in carbon capture is investigated. In Chapter 1, the background of greenhouse gas emissions is reviewed and discussed, followed by the development of carbon capture technologies and different adsorbents used in post-combustion carbon capture. An introduction to metal organic frameworks is then presented, including a literature review of the research to date, and various synthesis methods including batch and continuous routes. The last part of this chapter presents a literature review on how pre-synthetic design and post-synthetic modification synthesis of MOFs can be achieved. The theories and introductions of the characterization techniques used in this thesis are discussed in detail in Chapter 2. Chapter 3 discusses a new batch method for the efficient synthesis of micro-sized HKUST-1 with high yield (84%) under mild conditions. Different activation methods are conducted in the washing process. Both ethanol and methanol are tested to remove the impurities in pores of the samples. Finally, the optimal sample of HKUST-1 achieved is shown to produce a relatively high surface area (1615 m2/g) with a CO2 adsorption of 8.1% (measured by TGA at 1 atm and 27 oC). A step increase in the surface area is made by immersing the powders into a solution consisting of NaCl, water and methanol. Nano scale HKUST-1 is synthesized by adding trimethylamine (TEA) solution with the organic ligand precursor. The reaction rate is accelerated with this case because TEA solution is able to deprotonate the trimesic acid (the organic ligand). The method for nano scale HKUST-1 synthesis is the focus of Chapter 4. Chapter 5 reports the continuous synthesis process of HKUST-1 and ZIF-8. This work builds on previous work at Nottingham. A counter-current Nozzle reactor is used in this work. The products were compared with commercial equivalents. Post-synthetic modification of HKUST-1 was made to improve the hydrophobicity of HKUST-1 to extend its resilience to breakdown in the presence of moisture. In Chapter 6, a hybrid material TiO2@ZIF-8 is synthesized using the same reactor. Different reactor configurations were also used to generate a range of different products that are then compared. To conclude, a summary of the work conducted in this thesis is presented in Chapter 7, followed by a discussion on potential future work.

Accelerated carbonation technology (ACT) could be used for the stabilisation of hazardous wastes, remediation of contaminated soils and re-use/recycling of various waste streams. ACT has also potential for storing anthropogenic CO2 emissions into mineral silicates and alkaline waste residues via mineral or waste carbonation. Compared to ocean and geological storage, mineral and waste carbonation offer several advantages such as long-term storage and low monitoring requirements. Currently, the biggest challenge of mineral carbonation is the low conversion rate of calcium and magnesium-based minerals into thermodynamically stable carbonates under ambient temperature and pressure. Also, literature offers little information about physical techniques or chemical substances that could enhance the efficacy of accelerated carbonation of alkaline wastes. In this study, various carbonation techniques were applied for increasing the carbonation reactivity of magnesium hydroxide. The experiments were conducted under low temperature and pressure, while the maximum reaction time was 24 hours. Under these conditions the associated costs are kept to a minimum. The possibility of producing monolithic products with value-added was investigated by using blended mixtures of magnesium and calcium hydroxide. These mixtures were cured in carbon dioxide for 7 and 28 days and their physical properties were measured and compared with the properties for normal and lightweight concrete. Moreover, several alkaline residues were carbonated with the aid of ultrasound and four candidate catalysts (acetic acid, ethanol, sodium hypochlorite and sodium nitrite) and their CO2 uptake was measured. During sonication the variables: ultrasonic frequency, water content and treatment time were examined, while the applied chemicals were added at three different molarities (0.1 M, 0.5M and 2.5M). Throughout this work a number of analytical techniques were used for the characterisation of the raw and carbonated materials. These techniques included XRay fluorescence, X-ray diffraction, wet laser analysis, total organic carbon analysis and scanning electron microscopy. The results showed that the CO2-reactivity of Mg(OH)2 was low due to thermodynamic constraints that inhibited the rapid diffusion of CO2 into the system. The mixtures composed of pure Mg showed improved compressive strength and bulk density. In addition, sonication at low water content was weak, as there was lack of enough water to facilitate cavitation. On the other hand, at high water content the achieved CO2 uptake of the products increased by up to four times, as the wet conditions enhanced the cavitation of the solid particles. Finally, it was found that ethanol and acetic acid promoted the hydration rate of CO2 during accelerated carbonation, while minerals phase analysis did not reveal the formation of toxic by-products. In conclusion, the findings of this study proved that sonication depends highly on water content and is favoured at wet conditions. Furthermore, acetic acid and ethanol are two chemicals with potential to ameliorate the accelerated carbonation of various industrial wastes without the formation of un-desired or toxic compounds.

The rapid development of palm oil industry in Malaysia has generated significant amount of solid and liquid wastes, contributing to major environmental issues in the past five decades. Palm oil residues such as palm kernel shell (PKS), empty fruit bunch (EFB) and palm oil sludge (POS) are difficult to be disposed of. Thus, the potential application of the oil palm wastes for synthesis of value added products such as adsorbents for heavy metals removal and solid biochars for fuel generation, are presented in this thesis. In the past three decades, industrialisation and urbanisation in Malaysia have led to an increase of heavy metals, such as copper, cadmium, lead, zinc, chromium and nickel, in the rivers and lakes. The presence of the heavy metals is causing harmful effects on the aquatic environment and human health, hence it is necessary to control the discharge of industrial effluent into the environment. Among various heavy metals abatement technologies, adsorption is by far the most promising technique due to its relatively easy operation and high efficiency. However, adsorption is associated with costly adsorbent, such as activated carbon which is usually made from non-renewable resource. This has motivated many researchers to investigate and develop cost effective adsorbents for the removal of heavy metals. In this research, biosorbent was prepared from palm oil sludge. The preparation steps were relatively simple and low cost, involving mechanical treatments such as drying, milling and sieving. The POS biosorbent was tested on removal of copper (Cu2+) and cadmium (Cd2+), followed by process optimisation using response surface methodology (RSM), based on central composite design (CCD). Comparing between one-factor-at-a-time (OFAT) and RSM-CCD methods, both studies produced results which were in good agreement. The investigation was carried out to evaluate the effects of adsorbent dosage (W), initial pH, initial concentration (C0) and contact time (t), on the heavy metals removal. From optimisation study using RSM-CCD, the optimum adsorption parameters for Cu2+ removal were as follows: W = 0.3 g; pH 4.56; C0 = 200 mg L-1; t = 60 min, with maximum adsorption capacity (q) of 15.84 mg g-1, and for Cd2+ removal were as follows: W = 0.3 g; pH 5.8; C0 = 200 mg L-1; t = 60 min, with maximum q of 18.49 mg g-1. The adsorption equilibrium of Cu2+ and Cd2+ were best described by Langmuir and Freundlich models, respectively, based on the lowest sum of normalised error (SNE). The adsorption kinetic of Cu2+ and Cd2+ were best fitted with pseudo-second-order kinetic model. Thermodynamically, the adsorption processes were spontaneous, exothermic and feasible. Regeneration of POS biosorbent was carried out using hydrochloric acid (HCl) as the eluent, and the results indicated the high desorption efficiency for Cu2+ (up to 0.98) and Cd2+ (0.95) from the biosorbent, respectively. The POS biomass was also converted to POS-char by slow pyrolysis which was subsequently used in lead (Pb2+) adsorption study. The synthesis of POS-char was optimised by RSM-CCD based on simultaneous maximisation of biochar yield and q of Pb2+. The interactive effects of nitrogen flowrate (FN2), heating rate (HR), pyrolysis temperature (Tpyro) and pyrolysis time (tpyro) on the responses were investigated. It was determined that the maximum biochar yield was 80.35 % and q was 4.11 mg g-1, formed at the following slow pyrolysis conditions: FN2 = 30 mL min-1; HR = 10 °C min-1; Tpyro = 500 °C; tpyro = 30 min. In Pb2+ adsorption study, the optimum parameters determined by RSM-CCD optimisation were as follows: W = 0.3 g, pH 3.2, C0 = 200 mg L-1 and t = 60 min, with a maximum q of 21.76 mg g-1. The adsorption equilibrium of Pb2+ was best represented by Freundlich model. This finding indicated that the sorption sites in POS-char were heterogeneous. The kinetic study revealed that at low concentrations, the kinetic of adsorption complied with pseudo-first-order model, while at high concentrations, it obeyed pseudo-second-order model. Regeneration of POS-char was successfully conducted using HCl and the adsorbent exhibited reusability up to 5 adsorption-desorption cycles, with the desorption efficiencies between 0.58 and 0.99. Beyond 3 cycles, the adsorbent showed noticeable structural damage. Overall, the adsorption of Pb2+ onto POS-char was spontaneous, exothermic and feasible. The slow pyrolysis of PKS and EFB to biochars was investigated by simultaneously varying factors such as FN2, HR, Tpyro and tpyro. The synthesis parameters were optimised by RSM-CCD with respect to multiple responses, including biochar yield, higher heating value (HHV) and energy yield. The interactive effects of FN2, HR, Tpyro and tpyro on the three responses were in good agreement with literature data. The determined optimum conditions for PKS-char and EFB-char production by slow pyrolysis were as follows: FN2 = 30 mL min-1, HR = 18.9 – 20.0 °C min-1, Tpyro = 500.0 – 504.3 °C and tpyro = 30 min. The combustion kinetic on the optimised PKS-char and EFB-char were found to possess favourable combustion characteristics such as low activation energy (Ea), high energy yield and HHV. Overall, the combustion of PKS-char and EFB-char occurred in multi-step kinetics behaviour until burnout. The cost analysis on synthesis of PKS-char, EFB-char, POS-char and POS biosorbent was performed based on independent case studies which considered the capital and operating costs. The results revealed that addition of the thermochemical conversion plant to existing oil palm mill was highly feasible. The unit cost for production of PKS-char, EFB-char, POS-char and POS were USD$ 3.94 kg-1, USD$ 1.21 kg-1, USD$ 2.17 kg-1 and USD$ 0.19 kg-1 ̧ respectively.

Biomass-burning haze (BBH) is an environmental concern which has a tremendous impact on human health and the economy in Southeast Asia (SEA). One of the worst haze events to ever hit Peninsular Malaysia occurred in June 2013 due to smoke from Riau, Central Sumatra. While biomass-burning in the region is common, the early occurrence of a haze episode of this magnitude is uncharacteristic of the seasonality of extreme fire events which usually occur between August and October in the Maritime Continent (MC). Previous studies on the June 2013 event mostly include statistical studies of the impacts of haze on air quality and health. Therefore, this study aims to investigate the phenomenology of this peculiar haze event and its underlying meteorological forcing agents. The aerosol and meteorological environment during the event is examined using the Moderate Resolution Imaging Spectroradiometer (MODIS) active fire hotspot detections and aerosol optical thickness (AOT) retrievals, satellite based precipitation retrievals and meteorological indices. Particular attention is given to El Niño Southern Oscillation (ENSO) and Madden-Julian Oscillation (MJO) conditions since these phenomena influence inter-annual and intra-seasonal fire-activity, respectively, as well as the influence of tropical cyclones (TC) over the South China Sea. The above datasets are then supported by a WRF-Chem nested simulation to provide a comprehensive picture of the event’s meteorology and aerosol transport phenomenology. Indeed, while the use of weather models to study BBH has become more popular, more modelling efforts need to be put into studying the June 2013 haze event to identify the mechanisms of long range transport of haze. A set of 13 sensitivity simulations are run to determine the physics settings which best represent the meteorology over the model domain during the June 2013 haze episode. The physics options used in the sensitivity simulations are selected based on previous WRF physics sensitivity studies and work which include WRF simulations with domains over Asia and SEA. In particular, the microphysics, cumulus parameterisation and planetary boundary layer (PBL) schemes are looked into to obtain the best agreement to observation data. The output from the sensitivity simulations are evaluated with satellite based precipitation retrievals and ground station data over Malaysia. The simulations run with the Lin microphysics scheme, Betts-Miller-Janjić (BMJ) cumulus parameterisation scheme and Mellor-Yamada-Janjić (MYJ) planetary boundary layer scheme performed best overall. These best settings, based on the sensitivity studies, are then used in the numerical simulations which are evaluated with satellite and ground station data. The evaluation shows that model produces similar patterns and magnitudes of AOT and successfully captures the variations in smoke plume height when compared to MODIS AOD and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) aerosol extinction profile datasets. The analysis of the time series ENSO conditions and MODIS fire count show that while extreme fire events are more characteristic of El Niño years, the MODIS fire count over the MC in June for the years 2001–2015 was highest in 2013 when neutral conditions prevailed. Although, the mean daily precipitation for June 2013 was below average for June for the years 2003–2015. In addition, the highest ratio of 0.89 of fire count for SPM to MC for any month for the period 2001–2015 was recorded in June 2013. An early and active TC season, which could have been the result of a strong transiting MJO, occurred in June 2013. The results show that the combined induced subsidence and flow enhancement due to TC Bebinca and the dry phases of the strong MJO event contributed to the event. The simulations further show that downward vertical motion of at least 6 cm s-1 prevailed over Sumatra on 22 June when TC Bebinca was most intense, while upward vertical motion reaching at least 9 cm s-1 prevailed over the same region before TC Bebinca on 17 June. Indeed, smoke sources were concentrated under this particular region of subsidence, where surface PM2.5 concentrations reached at least 1000 μg m-3 on 22 June. Vertical cross-sections across the model domain also show that subsidence during phase 6 of the MJO prevailed over Sumatra. Intense and early TC seasons over the Western North Pacific can therefore be an indication of the occurrence of early and extreme haze events over the MC. The numerical simulations are also used to study the convective mechanisms which are responsible for uplifting biomass-burning haze in the troposphere. These mechanisms over Sumatra and Peninsular Malaysia are under-studied and their physical mechanisms remain unclear. The PM2.5 mass concentration, vertical wind speed plots at different levels and vertical cross-sections of major smoke plumes are analysed and the corresponding convective mechanisms identified. Three main convective mechanisms are identified, namely, orographic motion over the Barisan Mountains of Indonesia, morning convergence over the strait of Malacca and orographic motion over Peninsular Malaysia. Results show that smoke is lifted to heights of at least 10 km in the atmosphere due to orographic lifting over Peninsular Malaysia while the average plume height increased to higher than 2 km as TC Bebinca subsided, due to the resulting decrease in subsidence. The identified mechanisms are able to uplift the biomass-burning emissions to the upper troposphere and this could have significant long-range transport and global climatic effects.

Yangtze River Delta (YRD) region experiences severe haze pollution as a result of rapid economy growth and urbanization during recent decades. Its annual average PM2.5 (particulate matter with aerodynamic diameter ≤ 2.5μm) concentration often exceeded the National Ambient Air Quality Standards of China–Grade II (35 μg m-3) and this occurs not only in urban areas but also in suburban and rural areas as well. One of the major contributors to the decreasing air quality in this region is biomass burning. Hence, this research aims to study biomass burning impact on the air quality in YRD through the investigation of atmospheric fine aerosols. An intensive field sampling campaign was conducted at four representative sampling sites in urban, suburban and rural areas of this region from December 2014 to November 2015. The characteristics of PM2.5 samples that collected in this region were investigated through a comprehensive analysis of major components of aerosol samples, including major water soluble inorganic ions (WSII), trace metals, organic carbon (OC), elemental carbon (EC), polycyclic aromatic hydrocarbons (PAHs), biomass burning tracers and fungal spore tracers. The investigation of above mentioned components can provide a very comprehensive profile of PM2.5-related pollutants in YRD. In addition, air mass backward trajectory analysis and fire-spots analysis were also carried out in this study to identify air mass origins, pathways and fire events in this region. Positive matrix factorization (PMF) was also applied to estimate the contribution from biomass burning to fine aerosols in YRD. Both temporal and spatial trends of above pollutants were studied accordingly to set up seasonal and geographical profiles. In total, more than 240 PM2.5 samples were being analysed in this study. The annual average PM2.5 concentration in this region was 66.2 ± 37.7 μg m-3, and urban sites were observed with higher PM2.5 concentrations than the other two suburban and rural sites. The annual average concentration of total 12 WSII in YRD was 29.1 ± 19.9 μg m-3, dominated by SO42-, NO3-, NH4+, Cl-, and K+. The annual averaged concentration of total 20 metals in YRD was 2.8 ± 0.4 μg m-3, dominated by K, Al, Fe, Mg, Zn and V (> 100 ng m-3). The carcinogenic risk of Cr and As via ingestion is higher than the acceptable level for all residences in YRD. The annual average level of PM2.5-associated total carbon (TC) at YRD region was 14.3 ± 4.1 μg m-3, accounted for 26.2 (± 6.5) % of annual mean PM2.5 concentration. The annual averaged concentration of total 17 PAHs in YRD was 35.5 ± 12.3 ng m-3, dominated by retene, BkF, BbF, Ind, Bpe, Flt and Chr (> 2 ng m-3). The annual lifetime cancer risk of PAHs through inhalation exposure in YRD was 3.57 × 10-4. The annual average concentrations of levoglucosan and arabitol were 81.3 ± 18.2 ng m-3 and 5.6 ± 0.7 ng m-3 respectively. These compounds above exhibited similar seasonal patterns as PM2.5 with elevated level in winter and lower level in summer, except fungal spore tracers which showed the highest concentration in summer. In total, WSII, trace metals, TC, PAHs and organic tracers explained more than 69.8 % of total PM2.5 in YRD. The contribution from biomass burning to fine aerosols in YRD was 18.2%-37.4%. The concentration of biomass burning emitted PM2.5 ranged from 10.07 μg m-3 in spring to 27.60 μg m-3 in winter. Fine aerosols in southern YRD were contributed remarkably by fuel combustion such as coal and biomass burning, with less contributions from traffic emissions and soil origins, minor from sea salts. The contribution from coal combustion and biomass burning was more significant in winter and autumn than in spring and summer. The contribution from biomass burning decreased within the provincial capital municipality and the influence from biomass burning was more significant in rural area during autumn. In addition, the air mass backward trajectory analysis also showed that the contribution from transboundary transport of aerosols from highly polluted north China cannot be neglected.

No description available.

No description available.