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In the present study, Mg0.25Fe2.75O4 nanocatalyst for reduction of emissions in diesel engine was fabricated via urea-nitrate combustion method. The effect of urea concentrations as fuel on its structural characteristics and Oxygen Storage Capacity (OSC) was thoroughly investigated. The results of various characterization analyses showed that fuel ratio significantly affects crystallinity, textural, size and morphology of particles, and thermal stability of nanocatalyst. These are mainly due to increase in combustion temperature and duration. The Mg0.25Fe2.75O4 fabricated at fuel ratio of 2.5 times of stoichiometric ratio exhibited the lowest weight loss/high crystallinity (less than 1 wt %) and lowest lattice parameter (8.346 A) which are related to well diffusion of Mg cations into ferric oxide as host. The Raman and FTIR analyses showed the existence of strong peaks correspond to formation of tetrahedral and octahedral sublattices and also the formation of spinel structure of MgFe2O4. The reduction in crystalline size, obtained with higher amount of fuel, resulted in a higher surface area (23.6 m2/g), higher pore volume (0.0950 cc/g) and proper particle size distribution (25–35 nm). These cause a better catalytic activity. Moreover, the enhanced OSC (8661 μmol H2/g) along with shifting the reduction peaks to lower temperatures, as major attributes in relation to catalytic technologies, confirmed the strong effect of fuel ratio of 2.5 on fabrication process of Mg0.25Fe2.75O4. Finally, the highest reduction in HC (33%), CO (14-17%), PM1.0 (16%), and CO2 (12%) achieved, using the optimum sample-mixed diesel fuel at 90 ppm.

The industrial combustion of biomass, which has always been considered a source of clean and sustainable energy, might be phased out in China because it is believed to cause extremely high emissions of volatile organic compounds (VOCs), which are the key precursors in the formation of ozone and haze, although the emission factors have rarely been measured. In this study, the emissions of VOCs and several other air pollutants from typical industrial bagasse-fired boilers were measured for the first time. It was found that the emission factor (EF) of VOCs was 0.108 ± 0.034 g kg−1 (or 5.31 ± 1.68 g GJ−1 on an energy basis), which was roughly one order of magnitude lower than the officially recommended EF for industrial biomass combustion in China. In addition, the emissions of SO2, NOx and Hg from bagasse-fired boilers were even lower than those stipulated in the regulations for gas-fired boilers, with the exception of the particulate matter (PM), which was much lower than that produced during the open burning of biomass but higher than that from solid-fuel-fired boilers, likely as a result of the application of an ineffective dust removal device. It was demonstrated that the industrial combustion of biomass might produce much lower VOC emissions than expected and could help alleviate air pollution if biomass (at least bagasse) were used on a large scale instead of simply being burned in the field. In the future, dust removal devices with high efficiency should compulsorily be applied to industrial biomass boilers, and additional types of biomass fuel should be thoroughly evaluated to provide air-quality and energy policy makers with important insights.

Improving oxygen storage capacity (OSC) of metal oxides by doping with metal cations can produce a catalyst with superior properties to improve engine performance and reduce emissions. In this study, Mg cations were incorporated into a ferric oxide lattice to form Mg0.25Fe2.75O4 via the solution combustion method. The structure, texture, morphology, and oxygen storage capacity of the samples were deeply investigated. The catalytic activity of Mg0.25Fe2.75O4 was finally compared with Fe3O4 as a reference nanocatalyst in terms of its combustion emissions using a six-cylinder Cummins diesel engine. It was found that the doped catalyst presented high crystallinity containing a mixture of the spinel-type crystal lattice and α-Fe2O3 structure, which confirms the ability of the solution combustion method for the fabrication of well-crystalline catalysts. The crystalline structure, surface area, and porosities and vacancy of spinel structure of Mg doped catalyst compared to the inverse spinel structure of Fe3O4 affect OSC of the samples, such that a significant increase in OSC of Fe3O4 (7941 µmol/g) occurred by loading of Mg cations (8661 µmol/g). Based on the engine emissions results, synthesized nanocatalysts are beneficial for decreasing the hydrocarbon (HC), carbon monoxide (CO), and particle mass (PM1.0) emissions. More specifically, the effect of nanocatalysts OSC would be dominated by the impact of increased soot oxidation, leading to PM1.0 reduction.

Presented in this paper is an in-depth analysis of the impact of engine start during various stages of engine warm up (cold, intermediate, and hot start stages) on the performance and emissions of a heavy-duty diesel engine. The experiments were performed at constant engine speeds of 1500 and 2000 rpm on a custom designed drive cycle. The intermediate start stage was found to be longer than the cold start stage. The oil warm up lagged the coolant warm up by approximately 10 &deg, C. During the cold start stage, as the coolant temperature increased from ~25 to 60 &deg, C, the brake specific fuel consumption (BSFC) decreased by approximately 2% to 10%. In the intermediate start stage, as the coolant temperature reached 70 &deg, C and the injection retarded, the indicated mean effective pressure (IMEP) and the brake mean effective pressure (BMEP) decreased by approximately 2% to 3%, while the friction mean effective pressure (FMEP) decreased by approximately 60%. In this stage, the NOx emissions decreased by approximately 25% to 45%, while the HC emissions increased by approximately 12% to 18%. The normalised FMEP showed that higher energy losses at lower loads were most likely contributing to the heating of the lubricating oil.

Nitrogen (N) content in algae hydrothermal liquefaction (HTL) biocrude is high (5–8 wt%) and generally presumed to result in high NOx emissions during combustion. However, to our knowledge a very limited previous work on diesel engine performance and emissions of N-containing fuels. In order to investigate this issue, pyridine, an N-heterocyclic compound commonly found in algae biocrude, was blended with diesel fuel. This study investigated the influence of N in fuels, using a surrogate fuel to simulate algal biocrude, to determine the combustion behavior and emissions profile of an industrial multi-cylinder diesel engine. The presence of N in the fuel affected its physical properties. Density was slightly higher than neat diesel, while the viscosity, the flash point and the higher heating value (HHV) of the N-containing fuels reduced with increasing N content. The flash point of N-containing fuels were reduced, which affects the storage and transportation of the fuel. The engine load between 25 and 75% was observed to have an effect on engine performance parameters. Compared to diesel, N-containing fuels emitted both lower carbon monoxide (CO) and unburned hydrocarbons (HC). Increasing nitrogen oxides (NOx) emissions were observed with increasing N content in the fuels. At 50% and 75% loads, NOx emissions from N0.1 (0.1 wt% N), N0.5 (0.5 wt% N) and N2 (2 wt% N) were lower than for EUROIII. Particulate matter (PM) was lower for N-containing fuels compared to diesel fuel except for N0.1.

Metallic composition of diesel particulate matter, even though a relatively small proportion of total mass, can reveal important information regarding engine conditions, fuel/lubricating oil characteristics and for health impacts. In this study, a detailed investigation into the metallic elemental composition at different particle diameter sizes has been undertaken. A bivariate statistical analysis was performed in order to investigate the correlation between the metallic element, measured engine performance and engine emission variables. Major sources of metallic elements in the emitted particles are considered in this study, including the fuel and lubricating oil compositions, engine wear emissions and metal-containing dust in the ambient air. Metallic solid ultrafine-particles (Dp 100 nm). Calculated correlation matrices show a clear effect of engine load conditions and fuel S contents on particle number and mass emissions.

Over the years, oxygenated fuels such as biodiesel and alcohol fuels have been useful in reducing particulate matter (PM) emissions of diesel engines. The presence of oxygen in the fuel impacts the soot oxidation process and thus the morphology and nanostructural characteristics of soot particles change. The nanostructure characteristics of soot particles hold an importance for their oxidation reactivity and toxicity. Higher reactivity and exposure of soot particles to oxygen will affect the regeneration and filtration efficiency of diesel particulate filters. In this study, we investigate the impact of oxygen functional groups on morphology and nanostructure of soot particles by blending different types of essential oil in diesel. The test fuels were prepared by mixing orange oil, tea tree oil, eucalyptus oil and coconut biodiesel to keep an overall oxygen content of 0 and 2.2%. Transmission electron microscopy was used to investigate the physical changes in the nanostructure of soot particles. The primary particle diameter decreases, and fractal dimension of soot aggregates increases for oxygenated fuels. Microscopy reveals that the arrangement of carbon lamellae within the soot particles changes significantly with use of oxygenated as observed by the changes in fringe length, fringe tortuosity and fringe separation distance. Lower fringe length, higher fringe tortuosity and fringe separation distance shows disordered arrangement of carbon layers with more possibility of oxygen attack. The different structural characteristics for oils having same oxygen content shows that formation and structure of soot particles strongly depend upon chemical structure and composition of the fuel.

There are tons of waste tyres produced each year globally. Production of oil from the waste tyre not only manages the wastes but also produces fuels for compression ignition engines. In this investigation, a novel approach developed by Green Distillation Technologies in Australia was used to convert whole end of life tyres (ELTs) into carbon, steel, and tyre oil. The physicochemical properties of the tyre oil are similar to diesel fuel, and the fuel is miscible with diesel in any blended ratio. An engine experiment was conducted on a EURO IIIA diesel engine. All experiments were performed at constant speed and four different engine loads. Two blends (10% and 20%) of tyre oil were compared to reference diesel fuel. Exhaust emissions, including gaseous emissions, particulate matter (PM) and particulate number (PN) were investigated. The results indicate simultaneous reductions in both diesel PM and nitrogen oxides (NOx) emissions with the tyre oil blends when compared to diesel. NOx emissions were reduced by approximately 30% with both blends with respect to diesel. The reduction in PM and PN emissions were in the range of 35–60% and 5–20%, respectively. Carbon monoxide (CO) were increased by ∼ 10% compared to the reference diesel except at quarter load. Insignificant change in brake power (BP), brake mean effective pressure (BMEP) and brake thermal efficiency (BTE) were observe with the tyre oil blends. The engine remained compliant with its EURO IIIA guidelines during the use of the tyre oil blends. Based on the engine performance and emission result, the tyre oil could be alternative to traditional diesel fuel.

This study will focus on the detection of misfire using Acoustic emission sensor in a multi-cylinder diesel engine. Detection of misfire is important since this malfunction can cause the engine to stall in a short time. In order to investigate the misfire, an experimental engine was run with and without injection of the fuel in the first cylinder. The acoustic emission signal was acquired synchronously with the crank angle signal, in order to have a reference for the transformation from time to angular domain. The AE signal was then processed using the squared envelope spectrum to highlight angle-periodic modulations in the signal’s power (cyclic bursts). This study will present the effectiveness of this combination of sensor technology and signal processing to detect misfire in a six-cylinder diesel engine connected to a hydraulic dynamometer.

Presence or generation of reactive oxygen species (ROS) on/by particulate matter (PM) have been implicated in PM-induced health effects. Methodologies to quantify ROS concentrations vary widely both in detection and collection methods. However, there is currently an increasing emphasis on rapid collection and measurement due to observations of short half-live ROS. To address this problem, this manuscript details the design and characterization of a novel instrument named the Particle Into Nitroxide Quencher (PINQ). This instrument combines the BPEAnit ROS assay in conjunction with a purpose-built aerosol collection device, the insoluble aerosol collector (IAC). The IAC continuously collects PM regardless of size or chemistry directly into a liquid sample with a collection efficiency of 0.98 and a low cut-off size of < 20 nm. The sampling time resolution of the PINQ is one minute, with a limit of detection (LOD) of 0.08 nmol m−3 in equivalent BPEAnit-Me concentration per volume of air. This high sample time resolution and sensitivity is achieved due a combination of the highly concentrated IAC liquid sample and the rapid reaction and stability of the BPEAnit probe.

Essential oils are obtained from the non-fatty parts of a plant, such as the roots, bark, leaves, stems and flowers. These oils are mainly used in the natural medicine sector due to claimed health benefits, as well as the flavouring and fragrance sector, and the market has experienced rapid growth in recent years. The high quality required of the products leads to a very significant low-value waste stream, which is available for use in the transport and agricultural sectors. The use of essential oils in the compression ignition (CI) engine is a concept that has not yet been explored thoroughly. This paper analyses the available literature on the effect of essential oils and their blends on the performance, combustion characteristics and emission parameters of the CI engine. Regarding their properties, essential oils have similar properties to neat diesel. Engine performance using several essential oils and their blends improve brake thermal efficiency (BTE) and reduce brake-specific fuel consumption. A significant reduction in particulate matter (PM) emissions along with reduced hydrocarbon and carbon monoxide emissions has been reported in the literature. Furthermore, essential oils and their blends increase peak cylinder pressure and heat release rate (HRR) compared to neat diesel and biodiesel. However, most of the literature reported increased emissions of nitrogen oxides attributed to the lower cetane number and higher oxygen content. Due to having a low cetane number, essential oils can be used in CI engines by blending with either diesel or biodiesel. The rapid growth of the essential oil sector increases the likelihood of their utilization in CI engines in the future.

Introduction Diesel emissions have a high level of particulate matter which can cause inflammation and oxidative stress in the airways. A strategy to reduce diesel particulate matter and the associated adverse effects is the use of biodiesels and fuel additives. However, very little is known about the biological effects of these alternative emissions. The aim of this study is to compare the effect of biodiesel and triacetin/biodiesel emissions on primary human bronchial epithelial cells (pHBECs) compared to diesel emissions. Methods pHBECs were exposed to diesel, biodiesel (20%, 50% and 100% biodiesel derived from coconut oil) and triacetin/biodiesel (4% and 10% triacetin) emissions for 30 min at air-liquid interface. Cell viability (cellular metabolism, cell death, CASP3 mRNA expression and BCL2 mRNA expression), inflammation (IL-8 and IL-6 secretion), antioxidant production (HO-1 mRNA expression) and xenobiotic metabolism (CYP1a1 mRNA expression) were measured. Results Biodiesel emissions (B50) reduced cell viability, and increased oxidative stress. Triacetin/biodiesel emissions (B90) decreased cell viability and increased antioxidant production, inflammation and xenobiotic metabolism. Biodiesel emissions (B100) reduced cell viability, and increased IL-8 secretion and xenobiotic metabolism. Conclusions Biodiesel substitution in diesel fuel and triacetin substitution in biodiesel can increase the adverse effects of diesel emissions of pHBECs. Further studies of the effect of these diesel fuel alternatives on pHBECs are required.

Internally and externally mixed aerosols present significant challenges in assessing the hygroscopicity of each aerosol component. This study presents a new sampling technique which uses differences in volatility to separate mixtures and directly examine their respective composition and hygroscopic contribution. A shared thermodenuder and unheated bypass line are continuously cycled between an aerosol mass spectrometer and a volatility and hygroscopicity tandem differential mobility analyser, allowing real-time comparative analysis of heated and unheated aerosol properties. Measurements have been taken of both chamber-generated secondary organic aerosol and coastal marine aerosol at Cape Grim, Australia, to investigate system performance under diverse conditions. Despite rapidly changing aerosol properties and the need to restrict analysis to a narrow size range, the former experiment separated the hygroscopic influences of ammonium sulfate and two distinct organic components with similar oxygen to carbon ratios but different volatilities. Analysis of the marine aerosol revealed an external mixture of non-sea-salt sulfates and sea spray aerosol, which likely shared similar volatile fractions composed of sulfuric acid and a non-hygroscopic organic component.

Introduction: Diesel particulate matter can cause inflammation and oxidative stress in the airways. A strategy to reduce adverse effects associated with particulate matter in diesel emissions is the use of biodiesels and fuel additives such as triacetin, but very little is known about the health effects of these alternative emissions. The aim of this study is to evaluate the effects of biodiesel and triacetin/biodiesel emissions on primary human bronchial epithelial cells (pHBECs) in comparison to conventional diesel emissions. Methods: Primary HBECs were differentiated at air-liquid interface and exposed to diesel (D100), biodiesel (B20, B50 and B100: 20%, 50% and 100% biodiesel derived from waste cooking oil, respectively) and triacetin/biodiesel (B96 and B90: 4% and 10% triacetin in biodiesel, respectively) emissions for 30 minutes. Indicators of cell viability, inflammation, antioxidant production and xenobiotic metabolism were measured. Results: Biodiesel and triacetin substitution altered the particulate matter composition of the diesel emissions. B50, B90 and B100 significantly increased percentage cell death (75%, 60.9 and 49%, respectively). B50 and B90 significantly increased HO-1 mRNA expression (16.9-fold and 18.3-fold increase, respectively). B90 and B100 significantly increased IL-8 secretion (6.9-fold and 3-fold increase, respectively). Conclusions: Biodiesel fuels and fuel additives (triacetin) reduce particulate matter in diesel emissions, but have adverse effects on bronchial epithelial cell viability, metabolism and antioxidant production, compared to conventional diesel emissions. Further studies of the effect of diesel fuel alternatives on pHBECs are required.

Air pollution exposure is associated with a range of adverse health effects, including cardiovascular and respiratory diseases. Particle-bound ROS has been recognised as one of the prevailing parameters to indicate the toxic potential of airborne particulate matter (PM). The temporal variability of particle-bound ROS is a very important metric crucial for the improvement of public health and risk assessment policies. To our knowledge this is the first study aiming to investigate diurnal ROS profiles in both the particle and gas phase and associate them with diurnal variations of important pollutants. For that purpose, we have successfully applied a new instrument to continuously monitor diurnal ROS profiles at two locations in Hong Kong: a busy roadside and an urban background. Data was collected over both the working week and during weekends. We have observed a high correlation between particle-bound ROS and lower concentrations of black carbon (BC) at the roadside during the working week. These associations were less significant over the weekend and at all times with ozone. Our results suggest that most of the particle-bound ROS from both the particle and the gas phase arises from fresh emission sources directly from the traffic. A very interesting observation came out as a result of this study where measured ROS concentration was decreasing with the rise of ozone in conjunction with particle number, suggesting potential role of ROS in particle growth and aging.

Essential oils are derived from not-fatty parts of plants and are mostly used in aromatherapy, as well as cosmetics and perfume production. The essential oils market is growing rapidly due to their claimed health benefits. However, because only therapeutic grade oil is required in the medicinal sector, there is a substantial low-value waste stream of essential oils that can be used in the transportation and agricultural sectors. This study investigated the influence of orange, eucalyptus, and tea tree oil on engine performance and combustion characteristics of a multi-cylinder compression ignition engine. Orange, eucalyptus, and tea tree oil were blended with diesel at 10% by volume. For benchmarking, neat diesel and 10% waste cooking biodiesel-diesel blend were also tested. The selected fuels were used to conduct engine test runs with a constant engine speed (1500 RPM (revolutions per minute)) at four loads. As the load increased, frictional power losses decreased for all of the fuel samples and thus mechanical efficiency increased. At higher loads (75% and 100%), only orange oil-diesel blends produced comparable power to diesel and waste cooking biodiesel-diesel blends. Fuel consumption (brake and indicated) for the essential oil-diesel blends was higher when compared to base diesel and waste cooking biodiesel-diesel blends. Thermal efficiency for the essential oil-diesel blends was comparable to base diesel and waste cooking biodiesel-diesel blends. At higher loads, blow-by was lower for essential oil blends as compared to base diesel and waste cooking biodiesel-diesel blends. At 50% and 100% load, peak pressure was lower for all of the essential oil-diesel blends when compared to base diesel and waste cooking biodiesel-diesel blends. From the heat release rate curve, the essential oil-diesel blends ignition delay times were longer because the oils have lower cetane values. Overall, the low-value streams of these essential oils were found to be suitable for use in diesel engines at 10% blends by agricultural producers of these oils.

The disposal of waste rubber and scrap tyres is a significant issue globally; disposal into stockpiles and landfill poses a serious threat to the environment, in addition to creating ecological problems. Fuel production from tyre waste could form part of the solution to this global issue. Therefore, this paper studies the potential of fuels derived from waste tyres as alternatives to diesel. Production methods and the influence of reactor operating parameters (such as reactor temperature and catalyst type) on oil yield are outlined. These have a major effect on the performance and emission characteristics of diesel engines when using tyre derived fuels. In general, tyre derived fuels increase the brake specific fuel consumption and decrease the brake thermal efficiency. The majority of studies indicate that NOx emissions increase with waste tyre derived fuels; however, a few studies have reported the opposite trend. A similar increasing trend has been observed for CO and CO2 emissions. Although most studies reported an increase in HC emission owing to lower cetane number and higher density, some studies have reported reduced HC emissions. It has been found that the higher aromatic content in such fuels can lead to increased particulate matter emissions.

Over the past decade, a range of sensor technologies became available on the market, enabling a revolutionary shift in air pollution monitoring and assessment. With their cost of up to three orders of magnitude lower than standard/reference instruments, many avenues for applications have opened up. In particular, broader participation in air quality discussion and utilisation of information on air pollution by communities has become possible. However, many questions have been also asked about the actual benefits of these technologies. To address this issue, we conducted a comprehensive literature search including both the scientific and grey literature. We focused upon two questions: (1)Are these technologies fit for the various purposes envisaged? and (2)How far have these technologies and their applications progressed to provide answers and solutions? Regarding the former, we concluded that there is no clear answer to the question, due to a lack of: sensor/monitor manufacturers' quantitative specifications of performance, consensus regarding recommended end-use and associated minimal performance targets of these technologies, and the ability of the prospective users to formulate the requirements for their applications, or conditions of the intended use. Numerous studies have assessed and reported sensor/monitor performance under a range of specific conditions, and in many cases the performance was concluded to be satisfactory. The specific use cases for sensors/monitors included outdoor in a stationary mode, outdoor in a mobile mode,indoor environmentsand personal monitoring. Under certain conditions of application, project goals, and monitoring environments, somesensors/monitors were fit for a specific purpose. Based on analysis of 17 large projects, which reached applied outcome stage, and typically conducted by consortia of organizations, we observed that a sizable fraction of them (~ 30%) were commercial and/or crowd-funded. This fact by itself signals a paradigm change inair quality monitoring, which previously had been primarily implemented by government organizations. An additional paradigm-shift indicator is the growing use of machine learning or other advanced data processing approaches to improve sensor/monitor agreement with reference monitors. There is still some way to go in enhancing application of the technologies forsource apportionment, which is of particular necessity and urgency in developing countries. Also, there has been somewhat less progress in wide-scale monitoring of personal exposures. However, it can be argued that with a significant future expansion of monitoring networks, including indoor environments, there may be less need for wearable or portable sensors/monitors to assess personal exposure. Traditional personal monitoring would still be valuable where spatial variability of pollutants of interest is at a finer resolution than the monitoring network can resolve.

Respirable particulate matter present in outdoor and indoor environments is a health hazard. The particle concentrations can quickly change, with steep gradients on short temporal and spatial scales, and their chemical composition and physical properties vary considerably. Existing networks of aerosol particle measurements consist of limited number of monitoring stations, and mostly aim at assessment of compliance with air quality legislation regulating mass of particles of varying sizes. These networks can now be supplemented using small portable devices with low-cost sensors for assessment of particle mass that may provide higher temporal and spatial resolution if we understand the capabilities and characteristics of the data they provide. This paper overviews typical currently available devices and their characteristics. In addition it is presented original results of measurement and modelling in the aim of one low-cost PM monitor validation.

The objective of this study was to examine the hydrothermal liquefaction of sugarcane bagasse using ethanol and black liquor (BL) in a pilot scale. Combinations of co-solvents (ethanol/ water, ethanol/BL) were studied at various concentrations and reaction conditions. The maximum oil yield of 61% was achieved with a reaction temperature of 300 °C for 30 min and using pure BL as a solvent, while the highest higher heating value (HHV) was obtained from a 50:50 ethanol-BL mixture. The oils contained alcohols, esters, phenolic compounds, aromatics, and heterocyclics. The O/C and H/C ratios of the oil were comparable with traditional biodiesel and commercial diesel. Although this study showed there are some improvements to be made to improve the chemical composition, the approach has potential for large-scale production of a substitute for fossil-fuel-based diesel.

This study is seeking to investigate the effect of non-thermal plasma technology in the abatement of particulate matter (PM) from the actual diesel exhaust. Ozone (O3) strongly promotes PM oxidation, the main product of which is carbon dioxide (CO2). PM oxidation into the less harmful product (CO2) is the main objective whiles the correlation between PM, O3 and CO2 is considered. A dielectric barrier discharge reactor has been designed with pulsed power technology to produce plasma inside the diesel exhaust. To characterise the system under varied conditions, a range of applied voltages from 11 kVPP to 21 kVPP at repetition rates of 2.5, 5, 7.5 and 10 kHz, have been experimentally investigated. The results show that by increasing the applied voltage and repetition rate, higher discharge power and CO2 dissociation can be obtained. The PM removal efficiency of more than 50% has been achieved during the experiments and high concentrations of ozone on the order of a few hundreds of ppm have been observed at high discharge powers. Furthermore, O3, CO2 and PM concentrations at different plasma states have been analysed for time dependence. Based on this analysis, an inverse relationship between ozone concentration and PM removal has been found and the role of ozone in PM removal in plasma treatment of diesel exhaust has been highlighted.

Biomass is an important energy resource for producing bioenergy and growing the global economy whilst minimising greenhouse gas emissions. Many countries, like Australia have a huge amount of biomass with the potential for bioenergy, but non-edible feedstock resources are significantly under-exploited. Hence it is essential to map the availability of these feedstocks to identify the most appropriate bioenergy solution for each region and develop supply chains for biorefineries. Using Australia as a case study,we present the spatial availability and opportunities for second and third generation feedstocks. Considerations included current land use, the presence of existing biomass industries and climatic conditions. Detailed information on the regional availability of biomass was collected from government statistics, technical reports and energy assessments as well as from academic literature. Second generation biofuels have the largest opportunity in New South Wales, Queensland and Victoria (NSW, QLD and VIC) and the regions with the highest potential for microalgae are Western Australia and Northern Territory (WA, NT), based on land use opportunity cost and climate. The approach can be used in other countries with a similar climate. More research is needed to overcome key technical and economic hurdles.

In the prospect of limited energy resources and climate change, effects of alternative biofuels on primary emissions are being extensively studied. Our two recent studies have shown that biodiesel fuel composition has a significant impact on primary particulate matter emissions. It was also shown that particulate matter caused by biodiesels was substantially different from the emissions due to petroleum diesel. Emissions appeared to have higher oxidative potential with the increase in oxygen content and decrease of carbon chain length and unsaturation levels of fuel molecules. Overall, both studies concluded that chemical composition of biodiesel is more important than its physical properties in controlling exhaust particle emissions. This suggests that the atmospheric aging processes, including secondary organic aerosol formation, of emissions from different fuels will be different as well. In this study, measurements were conducted on a modern common-rail diesel engine. To get more information on realistic properties of tested biodiesel particulate matter once they are released into the atmosphere, particulate matter was exposed to atmospheric oxidants, ozone and ultra-violet light; and the change in their properties was monitored for different biodiesel blends. Upon the exposure to oxidative agents, the chemical composition of the exhaust changes. It triggers the cascade of photochemical reactions resulting in the partitioning of semi-volatile compounds between the gas and particulate phase. In most of the cases, aging lead to the increase in volatility and oxidative potential, and the increment of change was mainly dependent on the chemical composition of fuels as the leading cause for the amount and the type of semi-volatile compounds present in the exhaust.

The effect of non-thermal plasma technology for particulate matter removal and nitrogen oxide emission reduction from diesel exhaust has been investigated. A sample of exhaust was cooled to the ambient temperature and passed through a dielectric barrier discharge reactor. This reactor was employed for producing plasma inside the diesel exhaust. A range of discharge powers by varying the applied voltage from 7.5 to 13.5 kV (peak–peak) at a frequency of 50 Hz has been evaluated during the experiments. Regarding the NOx emission concentration, the maximum removal efficiency has been achieved at energy density of 27 J/L. Soot, soluble organic fraction and sulphate components of diesel particulate matter have been analysed separately, and the consequence of plasma exposure on particle size distribution on both the nucleation and accumulation modes has been studied. Plasma was found to be very effective for soot removal, and it could approach complete removal efficiency for accumulation mode particles. However, when applied voltage approached 12 kV, the total number of nucleation mode particles increased by a factor of 50 times higher than the total particle numbers at the reactor inlet. This increase in nucleation mode particles increased even more when applied voltage was set at 13.5 kV.

The current study investigates the opportunity of using Licella biofuel as a partly renewable fuel provided by Licella P/L. Hereafter this fuel will be referred to as Licella biofuel. The renewable component of the Licella biofuel was made from the hydrothermal conversion of Australian pinus radiata wood flour using Licella’s proprietary Cat-HTR™ technology. The diesel-soluble component of the hydrothermal product was extracted into road diesel to give a blended fuel containing approximately 30% renewable material with the balance from diesel. This was further blended with a regular diesel fuel (designated R0) to give fuels for testing containing 5%, 10% and 20% renewable fuel (designated R5, R10 and R20). Some of the key fuel properties were measured for R30 and compared with those of regular diesel fuel. The engine experiment was conducted on a four-cylinder turbocharged common rail direct injection diesel engine. All experiments were performed with a constant speed and five different engine loads. Exhaust emissions including particulate matter (PM) mass and numbers, nitric oxide (NO), total unburnt hydrocarbon (THC), carbon dioxide (CO2) and performance parameters including brake power (BP), indicated power (IP), brake mean effective pressure (BMEP), indicated mean effective pressure (IMEP), mechanical efficiency (ME), brake thermal efficiency (BTE) and brake specific energy consumption (BSEC) were investigated for all four blends (R0, R5, R10 and R20). Among other engine parameters, in-cylinder pressure, heat release rate (HRR) and pressure (P) versus volume (V) diagrams were also investigated for the four fuel blends.

Volatility-hygroscopicity tandem differential mobility analyzer measurements were used to infer the composition of sub-100 nm diameter Southern Ocean marine aerosols at Cape Grim in November and December 2007. This study focuses on a short-lived high sea spray aerosol (SSA) event on 7–8 December with two externally mixed modes in the Hygroscopic Growth Factor (HGF) distributions (90% relative humidity (RH)), one at HGF > 2 and another at HGF~1.5. The particles with HGF > 2 displayed a deliquescent transition at 73–75% RH and were nonvolatile up to 280°C, which identified them as SSA particles with a large inorganic sea-salt fraction. SSA HGFs were 3–13% below those for pure sea-salt particles, indicating an organic volume fraction (OVF) of up to 11–46%. Observed high inorganic fractions in sub-100 nm SSA is contrary to similar, earlier studies. HGFs increased with decreasing particle diameter over the range 16–97 nm, suggesting a decreased OVF, again contrary to earlier studies. SSA comprised up to 69% of the sub-100 nm particle number, corresponding to concentrations of 110–290 cm−3. Air mass back trajectories indicate that SSA particles were produced 1500 km, 20–40 h upwind of Cape Grim. Transmission electron microscopy (TEM) and X-ray spectrometry measurements of sub-100 nm aerosols collected from the same location, and at the same time, displayed a distinct lack of sea salt. Results herein highlight the potential for biases in TEM analysis of the chemical composition of marine aerosols.

In this study, the biodiesel properties and effects of blends of oil methyl ester petroleum diesel on a CI direct injection diesel engine is investigated. Blends were obtained from the marine dinoflagellate Crypthecodinium cohnii and waste cooking oil. The experiment was conducted using a four-cylinder, turbo-charged common rail direct injection diesel engine at four loads (25%, 50%, 75% and 100%). Three blends (10%, 20% and 50%) of microalgae oil methyl ester and a 20% blend of waste cooking oil methyl ester were compared to petroleum diesel. To establish suitability of the fuels for a CI engine, the effects of the three microalgae fuel blends at different engine loads were assessed by measuring engine performance, i.e. mean effective pressure (IMEP), brake mean effective pressure (BMEP), in cylinder pressure, maximum pressure rise rate, brake-specific fuel consumption (BSFC), brake thermal efficiency (BTE), heat release rate and gaseous emissions (NO, NOx,and unburned hydrocarbons (UHC)). Results were then compared to engine performance characteristics for operation with a 20% waste cooking oil/petroleum diesel blend and petroleum diesel. In addition, physical and chemical properties of the fuels were measured. Use of microalgae methyl ester reduced the instantaneous cylinder pressure and engine output torque, when compared to that of petroleum diesel, by a maximum of 4.5% at 50% blend at full throttle. The lower calorific value of the microalgae oil methyl ester blends increased the BSFC, which ultimately reduced the BTE by up to 4% at higher loads. Minor reductions of IMEP and BMEP were recorded for both the microalgae and the waste cooking oil methyl ester blends at low loads, with a maximum of 7% reduction at 75% load compared to petroleum diesel. Furthermore, compared to petroleum diesel, gaseous emissions of NO and NOx, increased for operations with biodiesel blends. At full load, NO and NOx emissions increased by 22% when 50% microalgae blends were used. Petroleum diesel and a 20% blend of waste cooking oil methyl ester had emissions of UHC that were similar, but those of microalgae oil methyl ester/petroleum diesel blends were reduced by at least 50% for all blends and engine conditions. The tested microalgae methyl esters contain some long-chain, polyunsaturated fatty acid methyl esters (FAMEs) (C22:5 and C22:6) not commonly found in terrestrial-crop-derived biodiesels yet all fuel properties were satisfied or were very close to the ASTM 6751-12 and EN14214 standards. Therefore, Crypthecodinium cohnii- derived microalgae biodiesel/petroleum blends of up to 50% are projected to meet all fuel property standards and, engine performance and emission results from this study clearly show its suitability for regular use in diesel engines.

The dicarbonyls glyoxal and methylglyoxal have been measured with 2,4-dinitrophenylhydrazine (2,4-DNPH) cartridges and high-performance liquid chromatography (HPLC), optimised for dicarbonyl detection, in clean marine air over the temperate Southern Hemisphere (SH) oceans. Measurements of a range of dicarbonyl precursors (volatile organic compounds, VOCs) were made in parallel. These are the first in situ measurements of glyoxal and methylglyoxal over the remote temperate oceans. Six 24 h samples were collected in summer (February–March) over the Chatham Rise in the south-west Pacific Ocean during the Surface Ocean Aerosol Production (SOAP) voyage in 2012, while 34 24 h samples were collected at Cape Grim Baseline Air Pollution Station in the late winter (August–September) of 2011. Average glyoxal mixing ratios in clean marine air were 7 ppt at Cape Grim and 23 ppt over Chatham Rise. Average methylglyoxal mixing ratios in clean marine air were 28 ppt at Cape Grim and 10 ppt over Chatham Rise. The mixing ratios of glyoxal at Cape Grim are the lowest observed over the remote oceans, while mixing ratios over Chatham Rise are in good agreement with other temperate and tropical observations, including concurrent Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) observations. Methylglyoxal mixing ratios at both sites are comparable to the only other marine methylglyoxal observations available over the tropical Northern Hemisphere (NH) ocean. Ratios of glyoxal : methylglyoxal > 1 over Chatham Rise but < 1 at Cape Grim suggest that a different formation and/or loss processes or rates dominate at each site. Dicarbonyl precursor VOCs, including isoprene and monoterpenes, are used to calculate an upper-estimate yield of glyoxal and methylglyoxal in the remote marine boundary layer and explain at most 1–3 ppt of dicarbonyls observed, corresponding to 10% and 17% of the observed glyoxal and 29 and 10% of the methylglyoxal at Chatham Rise and Cape Grim, respectively, highlighting a significant but as yet unknown production mechanism. Surface-level glyoxal observations from both sites were converted to vertical columns and compared to average vertical column densities (VCDs) from GOME-2 satellite retrievals. Both satellite columns and in situ observations are higher in summer than winter; however, satellite vertical column densities exceeded the surface observations by more than 1.5 × 1014 molecules cm−2 at both sites. This discrepancy may be due to the incorrect assumption that all glyoxal observed by satellite is within the boundary layer, or it may be due to challenges retrieving low VCDs of glyoxal over the oceans due to interferences by liquid water absorption or the use of an inappropriate normalisation reference value in the retrieval algorithm. This study provides much-needed data to verify the presence of these short-lived gases over the remote ocean and provide further evidence of an as yet unidentified source of both glyoxal and also methylglyoxal over the remote oceans.

Several cell-free assays are currently used to quantify and detect the Reactive Oxygen Species (ROS). All of them have certain limitations, do not provide direct comparison of results and, to date, none of these assays have been acknowledged as the most suitable acellular assay and none has yet been adopted for investigation of potential PM toxicity. These assays include DTT, ascorbic acid, DCFHDA and PFN assays which have been used in measurements of the particles generated from various combustion sources such as diesel engine, wood smoke (or biomass burning) and cigarette smoke, as well as for outdoor measurements. All the probes use different units for expressing redox properties of PM. Also, their reactivity is being triggered by different types of ROS. This limits the direct comparison of the results that are reporting the toxicity of the same aerosol type measured with various probes. This study is evaluating and comparing the various assays in order to develop deeper understanding of their capabilities, selectivity as well as improve understanding of the underlying chemical mechanisms. Keywords: DTT, DCFH-DA, PFN, BPEA-nit, Ascorbic acid, oxidative potential

A simple modular strategy for the synthesis of profluorescent nitroxide containing polymers is described. The incorporation of an epoxide as a pendant functionality on a polymer backbone synthesized using ATRP and subsequent nucleophilic ring-opening with sodium azide gave hydroxyl and azide functionality within a 3-bond radius. Orthogonal coupling chemistry then allowed the independent attachment of fluorophore and nitroxide groups in close proximity, giving rise to a profluorescent polymer. Validation of the viability of these materials as fluorescent sensors is demonstrated through efficient fluorescence switch-on observed when the materials are exposed to a model reductant or carbon-centred radical source.

Non-thermal plasma (NTP) has been introduced over the past several years as a promising method for nitrogen oxide (NOx) removal. The intent, when using NTP, is to selectively transfer input electrical energy to the electrons, and to not expend this in heating the entire gas stream, which generates free radicals through collisions, and promotes the desired chemical changes in the exhaust gases. The generated active species react with the pollutant molecules and decompose them. This paper reviews and summarizes relevant literature regarding various aspects of the application of NTP technology on NOx removal from exhaust gases. A comprehensive description of available scientific literature on NOx removal using NTP technology is presented, including various types of NTP, e.g. dielectric barrier discharge, corona discharge and electron beam. Furthermore, the combination of NTP with catalyst and adsorbent for better NOx removal efficiency is presented in detail. The removal of NOx from both simulated gases and real diesel engines is also considered in this review paper. As NTP is a new technique and is not yet commercialized, there is a need for more studies to be performed in this field.

Rationale: Exposure to diesel emissions (DE) has been associated with the development of lung cancer and increased COPD mortality in at-risk populations. The aim of this study was to investigate disease-specific changes in the expression of intracellular signalling genes in primary human bronchial epithelial cells (pHBECs) in response to diesel emission exposure using the Nanostring nCounter Intracellular Signalling RNA panel. Methods: 14 pHBEC lines (see Table 1) were exposed to DE for 30 minutes through the Cultex RFS. RNA was extracted using QIAGEN AllPrep kits. Gene expression changes of 192 intracellular signalling genes were assessed using the Nanostring nCounter Intracellular Signalling RNA panel. Quality control analysis and data analysis was performed using the nSolver Analysis Software v3.0. Results: DE exposure altered expression patterns of intracellular signalling genes in disease cohorts. Five genes had significantly altered expression levels after exposure to diesel emissions, when compared to FA. Conclusions: pHBECs may produce different intracellular signalling responses after diesel emission exposure, depending on the disease cohort. pHBECs increase the expression of immune regulating, inflammatory and anti-inflammatory genes after diesel emission exposure.

This study investigated particle and gaseous emission factors from a large cargo vessel for her whole voyage including at berth, manoeuvring and cruising. Quantification of these factors assists in minimising the uncertainty in the current methods of exhaust gas emission factor estimation. Engine performance and emissions from the main marine engine were measured on-board while the ship was manoeuvring and cruising at sea. Emissions of an auxiliary engine working at 55% of maximum continuous rating (MCR) were measured when the ship was at actual harbour stopovers. Gaseous and particle emission factors in this study are presented in g kWh-1 or # kWh-1, and compared with previous studies. Results showed that the SO2 emission factor is higher than that of previous studies due to the high sulphur content of the fuel used. The particle number size distributions showed only one mode for different operating conditions of the ship, with a peak at around 40-50 nm, which was dominated by ultrafine particles. Emission factors of CO, HC, PM and PN observed during ship manoeuvring were much higher than that of those recorded at cruising condition. These findings highlight the importance of quantification and monitoring ship emissions in close proximity to port areas, as they can have the highest impact on population exposure.

Establishing the relationship between marine boundary layer (MBL) aerosols and surface water biogeochemistry over the remote ocean is required to understand aerosol and cloud production processes, and also represent them accurately in Earth System Models and global climate projections. This was addressed in the SOAP (Surface Ocean Aerosol Production) campaign, which examined air-sea interaction over biologically-productive frontal waters east of New Zealand. This overview details the objectives, regional context, sampling strategy, and provisional findings of a pilot study, PreSOAP, in austral summer 2011, and the following SOAP voyage in late austral summer 2012. Both voyages characterised surface water and MBL composition in three phytoplankton blooms of differing species composition and biogeochemistry, with significant regional correlation observed between chlorophyll-a and DMSsw. Surface seawater dimethylsulfide (DMSsw) and associated air-sea DMS flux showed spatial variation during the SOAP voyage, with maxima of 25 nmol L−1 and 100 µmol m−2 d−1, respectively, recorded in a dinoflagellate bloom. Inclusion of SOAP data in a regional DMSsw compilation confirmed that the current climatological mean is an underestimate for this region of the South-west Pacific. Estimation of the DMS gas transfer velocity (kDMS) by independent techniques of eddy covariance and gradient flux showed good agreement, although both exhibited periodic deviations from model estimates. Flux anomalies were related to surface warming and sea surface microlayer enrichment, and also reflected the heterogeneous distribution of DMSsw and the associated flux footprint. Other aerosol precursors measured included the halides and various volatile organic carbon compounds, with the first measurements of the short-lived gases glyoxal and methylglyoxal in pristine Southern Ocean marine air indicating an unidentified local source. The application of a real-time clean-sector, contaminant markers, and a common aerosol inlet facilitated multi-sensor measurement of uncontaminated air. Aerosol characterisation identified variable Aitken mode, and consistent sub-micron sized accumulation and coarse modes. Sub-micron aerosol mass was dominated by secondary particles containing ammonium sulfate/bisulfate under light winds, with an increase in sea-salt under higher wind-speeds. MBL measurements and chamber experiments identified a significant organic component in primary and secondary aerosols. Comparison of SOAP aerosol number and size distributions reveals an underprediction in GLOMAP-mode aerosol number in clean marine air masses, suggesting a missing marine aerosol source in the model. The SOAP data will be further examined for evidence of nucleation events, and also for relationships between MBL composition and surface ocean biogeochemistry with the aim of identifying potential proxies for aerosol precursors and production.

As a biofuel feedstock, microalgae has good scalability and potential to supply a significant proportion of world energy compared to most types of biofuel feedstock. Hydrothermal liquefaction (HTL) is well-suited to wet biomass (such as microalgae) as it greatly reduces the energy requirements associated with dewatering and drying. This article presents experimental analyses of chemical and physical properties of bio-crude oil produced via HTL using a high growth-rate microalga Scenedesmus sp. in a large batch reactor. The overarching goal was to investigate the suitability of microalgae HTL bio-crude produced in a large batch reactor for direct application in marine diesel engines. To this end we characterized the chemical and physical properties of the bio-crudes produced. HTL literature mostly reports work using very small batch reactors which are preferred by researchers, so there are few experimental and parametric measurements for bio-crude physical properties, such as viscosity and density. In the course of this study, a difference between traditionally calculated values and measured values was noted. In the parametric study, the bio-crude viscosity was significantly closer to regular diesel and biodiesel standards than transesterified (FAME) microalgae biodiesel. Under optimised conditions, HTL bio-crude’s high density (0.97–1.04 kg·L−1) and its high viscosity (70.77–73.89 mm2·s−1) had enough similarity to marine heavy fuels. although the measured higher heating value, HHV, was lower (29.8 MJ·kg−1). The reaction temperature was explored in the range 280–350 °C and bio-crude oil yield and HHV reached their maxima at the highest temperature. Slurry concentration was explored between 15% and 30% at this temperature and the best HHV, O:C, and N:C were found to occur at 25%. Two solvents (dichloromethane and n-hexane) were used to recover the bio-crude oil, affecting the yield and chemical composition of the bio-crude.

In 2014, global demand for essential oils was 165 kt and it is expected to grow 8.5% per annum up to 2022. Every year Australia produces approximately 1.5k tonnes of essential oils such as tea tree, orange, lavender, eucalyptus oil, etc. Usually essential oils come from non-fatty areas of plants such as the bark, roots, heartwood, leaves and the aromatic portions (flowers, fruits) of the plant. For example, orange oil is derived from orange peel using various extraction methods. Having similar properties to diesel, essential oils have become promising alternate fuels for diesel engines. The present study explores the opportunity of using sweet orange oil in a compression ignition engine. Blends of sweet orange oil-diesel (10% sweet orange oil, 90% diesel) along with neat diesel fuel were used to operate a six-cylinder diesel engine (5.9 litres, common rail, Euro-III, compression ratio 17.3:1). Some key fuel properties such as: viscosity, density, heating value, and surface tension are presented. Engine performance (brake specific fuel consumption) and emission parameters (CO, NOX, and Particulate Matter) were measured to evaluate running with the blends. The engine was operated at 1500 rpm (maximum torque condition) with different loads. The results from the property analysis showed that sweet orange oil-diesel blend exhibits lower density, viscosity and surface tension and slightly higher calorific value compared to neat diesel fuel. Also, from the engine test, the sweet orange oil-diesel blend exhibited slightly higher brake specific fuel consumption, particulate mass and particulate number; however, the blend reduced the brake specific CO emission slightly and brake specific NOX emission significantly compared to that of neat diesel.

Establishing the relationship between marine boundary layer (MBL) aerosols and surface water biogeochemistry is required to understand aerosol and cloud production processes over the remote ocean and represent them more accurately in earth system models and global climate projections. This was addressed by the SOAP (Surface Ocean Aerosol Production) campaign, which examined air–sea interaction over biologically productive frontal waters east of New Zealand. This overview details the objectives, regional context, sampling strategy and provisional findings of a pilot study, PreSOAP, in austral summer 2011 and the following SOAP voyage in late austral summer 2012. Both voyages characterized surface water and MBL composition in three phytoplankton blooms of differing species composition and biogeochemistry, with significant regional correlation observed between chlorophyll a and DMSsw. Surface seawater dimethylsulfide (DMSsw) and associated air–sea DMS flux showed spatial variation during the SOAP voyage, with maxima of 25 nmol L−1 and 100 µmol m−2 d−1, respectively, recorded in a dinoflagellate bloom. Inclusion of SOAP data in a regional DMSsw compilation indicates that the current climatological mean is an underestimate for this region of the southwest Pacific. Estimation of the DMS gas transfer velocity (kDMS) by independent techniques of eddy covariance and gradient flux showed good agreement, although both exhibited periodic deviations from model estimates. Flux anomalies were related to surface warming and sea surface microlayer enrichment and also reflected the heterogeneous distribution of DMSsw and the associated flux footprint. Other aerosol precursors measured included the halides and various volatile organic carbon compounds, with first measurements of the short-lived gases glyoxal and methylglyoxal in pristine Southern Ocean marine air indicating an unidentified local source. The application of a real-time clean sector, contaminant markers and a common aerosol inlet facilitated multi-sensor measurement of uncontaminated air. Aerosol characterization identified variable Aitken mode and consistent submicron-sized accumulation and coarse modes. Submicron aerosol mass was dominated by secondary particles containing ammonium sulfate/bisulfate under light winds, with an increase in sea salt under higher wind speeds. MBL measurements and chamber experiments identified a significant organic component in primary and secondary aerosols. Comparison of SOAP aerosol number and size distributions reveals an underprediction in GLOMAP (GLObal Model of Aerosol Processes)-mode aerosol number in clean marine air masses, suggesting a missing marine aerosol source in the model. The SOAP data will be further examined for evidence of nucleation events and also to identify relationships between MBL composition and surface ocean biogeochemistry that may provide potential proxies for aerosol precursors and production., published version, peerReviewed

In aerosol research, a common approach for the collection of particulate matter (PM) is the use of filters in order to obtain sufficient material to undertake analysis. For subsequent chemical and toxicological analyses, in most of cases the PM needs to be extracted from the filters. Sonication is commonly used to most efficiently extract the PM from the filters. Extraction protocols generally involve 10 - 60 min of sonication. The energy of ultrasonic waves causes the formation and collapse of cavitation bubbles in the solution. Inside the collapsing cavities the localised temperatures and pressures can reach extraordinary values. Although fleeting, such conditions can lead to pyrolysis of the molecules present inside the cavitation bubbles (gases dissolved in the liquid and solvent vapours), which results in the production of free radicals and the generation of new compounds formed by reactions with these free radicals. For example, simple sonication of pure water will result in the formation of detectable levels of hydroxyl radicals. As hydroxyl radicals are recognised as playing key roles as oxidants in the atmosphere the extraction of PM from filters using sonication is therefore problematic. Sonication can result in significant chemical and physical changes to PM through thermal degradation and other reactions. In this article, an overview of sonication technique as used in aerosol research is provided, the capacity for radical generation under these conditions is described and an analysis is given of the impact of sonication-derived free radicals on three molecular probes commonly used by researchers in this field to detect Reactive Oxygen Species in PM.

In this study, an LPG fumigation system was fitted to a Euro III compression ignition (CI) engine to explore its impact on performance, and gaseous and particulate emissions. LPG was introduced to the intake air stream (as a secondary fuel) by using a low pressure fuel injector situated upstream of the turbocharger. LPG substitutions were test mode dependent, but varied in the range of 14-29% by energy. The engine was tested over a 5 point test cycle using ultra low sulphur diesel (ULSD), and a low and high LPG substitution at each test mode. The results show that LPG fumigation coerces the combustion into pre-mixed mode, as increases in the peak combustion pressure (and the rate of pressure rise) were observed in most tests. The emissions results show decreases in nitric oxide (NO) and particulate matter (PM2.5) emissions; however, very significant increases in carbon monoxide (CO) and hydrocarbon (HC) emissions were observed. A more detailed investigation of the particulate emissions showed that the number of particles emitted was reduced with LPG fumigation at all test settings - apart from mode 6 of the ECE R49 test cycle. Furthermore, the particles emitted generally had a slightly larger median diameter with LPG fumigation, and had a smaller semi-volatile fraction relative to ULSD. Overall, the results show that with some modifications, LPG fumigation systems could be used to extend ULSD supplies without adversely impacting on engine performance and emissions. © 2014 Elsevier Ltd. All rights reserved.

Biodiesels produced from different feedstocks usually have wide variations in their fatty acid methyl ester (FAME) so that their physical properties and chemical composition are also different. The aim of this study is to investigate the effect of the physical properties and chemical composition of biodiesels on engine exhaust particle emissions. Alongside with neat diesel, four biodiesels with variations in carbon chain length and degree of unsaturation have been used at three blending ratios (B100, B50, B20) in a common rail engine. It is found that particle emission increased with the increase of carbon chain length. However, for similar carbon chain length, particle emissions from biodiesel having relatively high average unsaturation are found to be slightly less than that of low average unsaturation. Particle size is also found to be dependent on fuel type. The fuel or fuel mix responsible for higher particle mass (PM) and particle number (PN) emissions is also found responsible for larger particle median size. Particle emissions reduced consistently with fuel oxygen content regardless of the proportion of biodiesel in the blends, whereas it increased with fuel viscosity and surface tension only for higher diesel–biodiesel blend percentages (B100, B50). However, since fuel oxygen content increases with the decreasing carbon chain length, it is not clear which of these factors drives the lower particle emission. Overall, it is evident from the results presented here that chemical composition of biodiesel is more important than its physical properties in controlling exhaust particle emissions.

With the advent of alternative fuels, such as biodiesels and related blends, it is important to develop an understanding of their effects on inter-cycle variability which, in turn, influences engine performance as well as its emission. Using four methanol trans-esterified biomass fuels of differing carbon chain length and degree of unsaturation, this paper provides insight into the effect that alternative fuels have on inter-cycle variability. The experiments were conducted with a heavy-duty Cummins, turbo-charged, common-rail compression ignition engine. Combustion performance is reported in terms of the following key in-cylinder parameters: indicated mean effective pressure (IMEP), net heat release rate (NHRR), standard deviation of variability (StDev), coefficient of variation (CoV), peak pressure, peak pressure timing and maximum rate of pressure rise. A link is also established between the cyclic variability and oxygen ratio, which is a good indicator of stoichiometry. The results show that the fatty acid structures did not have a significant effect on injection timing, injection duration, injection pressure, StDev of IMEP, or the timing of peak motoring and combustion pressures. However, a significant effect was noted on the premixed and diffusion combustion proportions, combustion peak pressure and maximum rate of pressure rise. Additionally, the boost pressure, IMEP and combustion peak pressure were found to be directly correlated to the oxygen ratio. The emission of particles positively correlates with oxygen content in the fuel as well as in the air-fuel mixture resulting in a higher total number of particles per unit of mass.

Compression ignition (CI) engine design is subject to many constraints, which present a multicriteria optimization problem that the engine researcher must solve. In particular, the modern CI engine must not only be efficient but must also deliver low gaseous, particulate, and life cycle greenhouse gas emissions so that its impact on urban air quality, human health, and global warming is minimized. Consequently, this study undertakes a multicriteria analysis, which seeks to identify alternative fuels, injection technologies, and combustion strategies that could potentially satisfy these CI engine design constraints. Three data sets are analyzed with the Preference Ranking Organization Method for Enrichment Evaluations and Geometrical Analysis for Interactive Aid (PROMETHEE-GAIA) algorithm to explore the impact of (1) an ethanol fumigation system, (2) alternative fuels (20% biodiesel and synthetic diesel) and alternative injection technologies (mechanical direct injection and common rail injection), and (3) various biodiesel fuels made from 3 feedstocks (i.e., soy, tallow, and canola) tested at several blend percentages (20-100%) on the resulting emissions and efficiency profile of the various test engines. The results show that moderate ethanol substitutions (∼20% by energy) at moderate load, high percentage soy blends (60-100%), and alternative fuels (biodiesel and synthetic diesel) provide an efficiency and emissions profile that yields the most "preferred" solutions to this multicriteria engine design problem. Further research is, however, required to reduce reactive oxygen species (ROS) emissions with alternative fuels and to deliver technologies that do not significantly reduce the median diameter of particle emissions. © 2013 American Chemical Society.

Influence of alternative fuels on diesel engine exhaust particle emission was investigated using an ultra-low sulfur diesel fuel as a baseline fuel where two biodiesels (canola & tallow), Fischer–Tropsch and bioethanol were used as alternative fuel. Both the biodiesels coming from canola and tallow feedstocks, as well as F-T were used as 100% to run the engine where up to 40% energy substitution by ethanol was achieved without any sacrifice of engine power output. It was found that up to 30% ethanol substitution reduced both particulate mass (PM) and particle number (PN) emission consistently for all load settings at 2000rpm, highest 59% reduction in PM and 70% reduction in PN observed at 100% load. As previously suggested the possible mechanism for the observed reduction is the oxidation of particulate matter by OH radicals which are in excess with ethanol fumigation. For 40% ethanol substitution some inconsistency was observed for PM emission at different loads but consistent reduction was found for PN. Condensation of unburned/partially burned hydrocarbons that later condense on existing soot might be responsible for this, as the maximum increase of PM was observed at quarter load where low in cylinder temperature favour to nucleation of unburned hydrocarbons. PM emission was also reduced in case of using 100% FT, and 100% biodiesel and the highest 90% reduction in PM was observed for biodiesel at 100% load with almost no difference between the two biodiesels itself. On the other side a considerable difference was observed between canola and tallow biodiesel in case of PN emission. Canola biodiesel increased PN, due to the presence of the nucleation mode, for almost an order of magnitude for all load and speed settings where no such increase was observed for tallow biodiesel.

Over the past few decades, biodiesel produced from oilseed crops and animal fat is receiving much attention as a renewable and sustainable alternative for automobile engine fuels, and particularly petroleum diesel. However, current biodiesel production is heavily dependent on edible oil feedstocks which are unlikely to be sustainable in the longer term due to the rising food prices and the concerns about automobile engine durability. Therefore, there is an urgent need for researchers to identify and develop sustainable biodiesel feedstocks which overcome the disadvantages of current ones. On the other hand, artificial neural network (ANN) modeling has been successfully used in recent years to gain new knowledge in various disciplines. The main goal of this article is to review recent literatures and assess the state of the art on the use of ANN as a modeling tool for future generation biodiesel feedstocks. Biodiesel feedstocks, production processes, chemical compositions, standards, physio-chemical properties and in-use performance are discussed. Limitations of current biodiesel feedstocks over future generation biodiesel feedstock have been identified. The application of ANN in modeling key biodiesel quality parameters and combustion performance in automobile engines is also discussed. This review has determined that ANN modeling has a high potential to contribute to the development of renewable energy systems by accelerating biodiesel research.

Highlights - The first review of shipping emissions in China - An overview of the broad field of ship emissions and their atmospheric impacts in China - Future work in shipping related air pollution field has been outlooked. Abstract China has > 400 ports, is home to 7 of 10 biggest ports in the world and its waterway infrastructure construction has been accelerating over the past years. But the increasing number of ports and ships means increasing emissions, and in turn, increasing impact on local and regional air pollution. This paper presents an overview of the broad field of ship emissions in China and their atmospheric impacts, including topics of ship engine emissions and control, ship emission factors and their measurements, developing of ship emission inventories, shipping and port emissions of the main shipping areas in China, and quantitative contribution of shipping emissions to the local and regional air pollution. There have been an increasing number of studies published on all the above aspects, yet, this review identified some critical research gaps, filling of which is necessary for better control of ship emissions, and for lowering their impacts. In particular, there are very few studies on inland ports and river ships, and there are few national scale ship emission inventories available for China. While advanced method to estimate ship emission based on ship AIS activities makes it now possible to develop high spatial- and temporal-resolution emission inventories, the ship emission factors used in Chinese studies have been based mainly on foreign measurements. Further, the contribution of ship emissions to air pollution in coastal cities, the dispersion of pollution plumes emitted by ships, or the chemical evolution process along the transmission path, have so far not been systematically studied in China.

Introduction: There is a growing need to find interventions against the adverse effects of diesel emissions. We tested an antioxidant as a therapeutic intervention against diesel emissions on human bronchial epithelial cells in vitro, and tested the effects of biodiesel as an alternative fuel source. Methods: 16HBE cells were cultured at air-liquid interface (ALI) and exposed to diesel or biodiesel (coconut oil (CO) and used oil (UO) substitution) emissions. After exposure, the cells were incubated with or without 5mM N-acetylcysteine (NAC) for 24 hours at 37°C. Cell viability and IL-8 secretion were measured. Results: Exposure to diesel emissions resulted in a significant decrease in cell viability, which was most effectively attenuated by the 20% CO substitution and 5mM NAC intervention. Both 20% CO substituted biodiesel and 5mM intervention were effective in reducing IL-8 secretion. Conclusions: Coconut oil-substituted biodiesel and NAC treatment may be protective interventions against the adverse effects of diesel emissions.

There is a lack of knowledge of how biomass burning aerosols in the tropics age, including those in the fire-prone Northern Territory in Australia. This paper reports chemical characterization and aging of aerosols monitored during the one month long SAFIRED (Savannah Fires in the Early Dry Season) field study, with an emphasis on chemical signature and aging of organic aerosols. The campaign took place in June 2014 during the early dry season when the surface measurement site, the Australian Tropical Atmospheric Research Station (ATARS), located in the Northern Territory, was heavily influenced by thousands of wild and prescribed bushfires. ATARS was equipped with a wide suite of instrumentation for gaseous and aerosol characterization. A compact time-of-flight aerosol mass spectrometer was deployed to monitor aerosol chemical composition. Approximately 80 % of submicron carbonaceous mass and 90 % of submicron non-refractory mass was composed of organic material. Ozone enhancement in biomass burning plumes indicated increased air mass photochemistry and increased organic aerosol and particle diameter with the aging parameter (f44) suggested secondary organic aerosol formation. Diversity of biomass burning emissions was illustrated through variability in chemical signature (e.g. wide range in f44, from 0.06 to 0.13) for five intense fire events. The background particulate loading was characterized using Positive Matrix Factorization (PMF). A PMF-resolved BBOA (biomass burning organic aerosol) factor comprised 24 % of the submicron non-refractory organic aerosol mass, confirming the significance of fire sources. A dominant PMF factor, OOA (oxygenated organic aerosol), made up 47 % of sampled aerosol fraction, illustrating the importance of aerosol aging in the Northern Territory. Biogenic IEPOX-SOA (isoprene epoxydiols-related secondary organic aerosol) was the third significant fraction of the background aerosol (28 %).