Derivation of synthetic fuel from waste plastic: investigation of engine operating characteristics on DI diesel engine

The utilization of plastic in day to day life is ever-increasing and has generated a large amount of plastic garbage that needs proper disposal to save the environment from harmful pollution. The plastic waste management becomes a pressing concern in the present scenario in developing countries like India. This research article evaluates the potential of synthetic fuel (SF) derived from waste plastics collected from the local shops. In this current investigation, the SF blends are tested in a direct injection diesel engine to analyze the performance and emission characteristics of the engine. Three different blends were made namely SF20, SF40, and SF60 on a volumetric basis and the tests were carried out. From the experimental results, it was found that brake thermal efficiency (BTE) of the fuel blends was reduced as compared with neat diesel operation regardless of loads whereas SF20 showed a similar trend as that of diesel operation. The analysis of the emission characteristics revealed that the SF20 blends reduced dangerous smoke and carbon monoxide emission as compared with other test fuels. From the overall results, SF20 showed superior performance and emission aspects as compared with other SF blends whereas the engine operated smoothly up to 60% of SF blending at all loading conditions.

     

An experimental study on usage of plastic oil and B20 algae biodiesel blend as substitute fuel to diesel engine

Usage of plastics has been ever increasing and now poses a tremendous threat to the environment. Millions of tons of plastics are produced annually worldwide, and the waste products have become a common feature at overflowing bins and landfills. The process of converting waste plastic into value-added fuels finds a feasible solution for recycling of plastics. Thus, two universal problems such as problems of waste plastic management and problems of fuel shortage are being tackled simultaneously. Converting waste plastics into fuel holds great promise for both the environmental and economic scenarios. In order to carry out the study on plastic wastes, the pyrolysis process was used. Pyrolysis runs without oxygen and in high temperature of about 250–300 °C. The fuel obtained from plastics is blended with B20 algae oil, which is a biodiesel obtained from microalgae. For conducting the various experiments, a 10-HP single-cylinder four-stroke direct-injection water-cooled diesel engine is employed. The engine is made to run at 1500 rpm and the load is varied gradually from 0 to 100 %. The performance, emission and combustion characteristics are observed. The BTE was observed to be higher with respect to diesel for plastic-biodiesel blend and biodiesel blend by 15.7 and 12.9 %, respectively, at full load. For plastic-biodiesel blend, the emission of UBHC and CO decreases with a slight increase in NO _x as compared to diesel. It reveals that fuel properties are comparable with petroleum products. Also, the process of converting plastic waste to fuel has now turned the problems into an opportunity to make wealth from waste.     

Assessment of metal contaminations leaching out from recycling plastic bottles upon treatments

Background, aims, and scope  

Heavy metal contaminants in environment, especially in drinking water, are always of great concern due to their health impact. Due to the use of heavy metals as catalysts during plastic syntheses, particularly antimony, human exposure to metal release from plastic bottles has been a serious concern in recent years. The aim and scope of this study were to assess metal contaminations leaching out from a series of recycling plastic bottles upon treatments.     

Origins and biological accumulation of small plastic particles in fur seals from Macquarie Island

One hundred and sixty four plastic particles (mean length 4.1 mm) recovered from the scats of fur seals (Arctocephalus spp.) on Macquarie Island were examined. Electron micrographs of 41 of the plastic particles showed that none could be identified as plastic pellet feedstock from their shapes. Commonly, such pellets are cylindrical and spherical. Instead, all the 164 plastic particles from the seal scats were angular particles of 7 colors (feedstock particles are normally opaque or white) and could be classified into 2 categories: i) fragmented along crystal lines and likely to be the result of UV breakdown; and ii) worn by abrasion (where striations were clearly visible) into irregular shapes with rounded corners. White, brown, green, yellow and blue were the most common colors. In composition, they came from 5 polymer groups; polyethylene 93%, polypropylene 4%, poly(1-Cl-1-butenylene) polychloroprene 2%, melamine-urea (phenol) (formaldehyde) resin 0.5%, and cellulose (rope fiber) 0.5%. The larger groups are buoyant with a specific gravity less than that of seawater. These small plastic particles are formed from the breakdown of larger particles (fragments). Their origin seems to be from the breakdown of user plastics washed ashore and ground down on cobbled beaches. Certainly most particles (70%) had attained their final form by active abrasion. It is hypothesized that the plastic particles were washed out to sea and then selected by size and consumed by individuals of a pelagic fish species, Electrona subaspera, who in turn were consumed by the fur seals. Thus, the particles were accumulated both by the fish and the seals in the usual process of their feeding.     

Organochlorine contaminants in eggs of seabirds in the Northwest Atlantic, 1968-1984

Eggs of three seabird species, double-crested cormorant (Phalacrocorax auritus). Leach's storm-petrel (Oceanodroma leucorhoa), and Atlantic puffin (Fratercula arctica) were collected at four-year intervals from 1968 to 1984, from colonies in eastern Canada and analyzed for organochlorines. This monitoring study was established to provide data on contamination of the marine environment and possible implications for seabird health. Long-term trend data are presented for PCBs, DDE, dieldrin, HCB, oxychlordane, heptachlor epoxide, HCH and mirex. DDE and PCBs declined significantly in all species from the Bay of Fundy. DDE declined significantly in puffins and petrels while PCBs declined only in petrels from the Atlantic coast of Newfoundland. Generally DDE declined more than PCBs. Dieldrin, oxychlordane, HCH and mirex levels decreased at some locations but were stable at others. Hexachlorobenzene and heptachlor epoxide levels remained steady or increased significantly, depending on the species and location. Organochlorine levels in cormorants from the St. Lawrence River estuary showed no significant trends.     

An introduction to critical loads

The critical loads approach to emission controls of gaseous pollutants is a concept with a short but eventful history. Despite difficulties with definitions and agreed values, its acceptance within the UN-ECE Convention on Long Range Transboundary Air Pollution has provided the impetus for developing methods to put critical loads to a practical use-the revision of the UNECE emission protocols for sulphur and nitrogen. Methodologies first focus upon quantifying a pollutant threshold at which harmful effects occur on particular sensitive receptors (usually biological species). This threshold is known as the critical load for deposited pollutants, and as the critical level for gaseous pollutants acting on receptors. To calculate a critical load, biological effects are usually 'translated' to critical chemical values, e.g. harmful effects on fish 'translate' to alkalinity or aluminium concentrations in water; thus, critical load calculations may be based upon the chemistry of a system. Such calculations may be performed using simple, steady-state models, whilst the use of more complex, dynamic models provides an insight into the past and future trends. Maps of critical loads can be drawn using calculated values, and maps of pollutant deposition data will then show geographical areas where critical loads are exceeded. Spatial emission-deposition models can identify sources contributing to areas of excess loads and quantify necessary emission reductions. Optimization procedures applied to such models can derive abatement strategies related to economic costs and critical load effects. The critical load calculations may also be used to underpin the setting of target loads; these are pollutant loads, determined by political agreement, which take account of social, economic and political considerations.     

An empirical map of critical loads of acidity for soils in Great Britain

The method used to produce a critical load map of acidity for soils in Great Britain is described. Critical loads were assigned to the dominant soil in each 1 km grid square of the UK national grid. Mineral soils were assigned a critical load based on mineralogy and chemistry, using approaches appropriate to UK conditions. Critical loads for peat soils are based primarily on a maximum acceptable reduction of peat pH, and results from laboratory equilibration studies. The map shows that soils with small critical loads (<0.5 kmol_c ha⁻¹ year⁻¹) i.e. highly sensitive to acidic deposition, dominate in the north and west of Britain; the south and east are dominated by soils with large critical loads, with small areas of more sensitive soils associated with sandy soil-forming materials. A modified critical load map illustrates the potential impact of agricultural liming on soil critical loads.     

负载对实际道路重型柴油车排放的影响研究

利用车载测试系统对重型柴油货车空载、50％负载和100％负载不同负载情况下在实际道路的排放进行测试,基于测试数据分析负载对重型柴油货车排放CO、HC、NOx和微小颗粒物(PM)等4种污染物的影响.不同速度区间和行驶模式下负载对排放的影响分析表明,在有负载时,大多数工况下4种污染物排放呈现增加趋势,但各速度区间和行驶模式下的增幅不尽相同,部分工况出现下降.空载时测试柴油车基于新欧洲行驶循环测试(NEDC)工况的标准化CO、HC、NOx和PM排放因子分别为3.38、0.39、6.27、0.39 g/km.对于柴油车重点污染物NOx和PM而言,与空载相比,50％负载时分别增加43％和59％,100％负载时分别增加62％和44％.     

Separation of plastic mixtures using liquid-fluidized bed technology

Separation of heavier-than-water plastic mixtures had been investigated via the fluidization of their packed beds induced by an upward flow of water. The samples examined were resin pellets and crushed plastic products including PVC, PET and PBT. On the onset of a flow, a mixed bed was swelled to the state of fluidization and separated into layers of respective resins depending on their density. The effects of the flow rate, an amount of the samples and their density difference were examined on the separation of resin pellets. Under an appropriate condition, the process was completed within a few minutes, and satisfactory separation was attained when the density difference of the samples exceeded 0.05 g cm-3. By using a column equipped with several sample outlets sorted resins could be recovered with their purity intact by withdrawing each layer successively from above through a suitable outlet. Multi-stage separation was also found to be effective in treating close-density samples. Compared with uniform-sized resin pellets, size distribution of crushed plastic samples deteriorated the separation to some extent.     

Dynamic modeling of organophosphate pesticide load in surface water in the northern San Joaquin Valley watershed of California

The hydrology, sediment, and pesticide transport components of the Soil and Water Assessment Tool (SWAT) were evaluated on the northern San Joaquin Valley watershed of California. The Nash-Sutcliffe coefficients for monthly stream flow and sediment load ranged from 0.49 to 0.99 over the watershed during the study period of 1992-2005. The calibrated SWAT model was applied to simulate fate and transport processes of two organophosphate pesticides of diazinon and chlorpyrifos at watershed scale. The model generated satisfactory predictions of dissolved pesticide loads relative to the monitoring data. The model also showed great success in capturing spatial patterns of dissolved diazinon and chlorpyrifos loads according to the soil properties and landscape morphology over the large agricultural watershed. This study indicated that curve number was the major factor influencing the hydrology while pesticide fate and transport were mainly affected by surface runoff and pesticide application and in the study area.     

The chemical form of mercury stored in South Atlantic seabirds

Concentrations of total mercury and organic (methyl) mercury were measured in the liver tissue of adults of 12 seabird species collected at colonies on Gough Island, South Atlantic Ocean. Total mercury levels showed both great intra- and interspecies variation, ranging from a mean of 1343.0 microg g(-1) dry weight in wandering albatrosses to a mean of 0.8 microg g(-1) dry weight in broad-billed prions. Organic mercury levels were less variable both between, but especially within, species. Organic mercury levels, expressed as a percentage of total mercury levels, ranged from a mean of 2.6% in wandering albatrosses up to a mean of 92.6% in littee shearwaters. Within each species, individuals with the highest total mercury levels tended to have the lowest percentage organic mercury, this trend being statistically significant in several species. Two species exhibited a significant positive correlation between organic mercury levels, in absolute terms, and total mercury levels. When all 12 species were considered, a highly significant negative correlation between mean percentage organic mercury and mean total mercury was found (rs = -0.888, P < 0.001). These results provide evidence to suggest that some seabirds may be capable of demethylating organic mercury in a species-dependent and that eliminatory pathways for the excretion of dietary mercury may influence the mode of response of a particular species.     

Endocrine disruptors in bottled mineral water: total estrogenic burden and migration from plastic bottles

Background, aim, and scope  Food consumption is an important route of human exposure to endocrine-disrupting chemicals. So far, this has been demonstrated by exposure modeling or analytical identification of single substances in foodstuff (e.g., phthalates) and human body fluids (e.g., urine and blood). Since the research in this field is focused on few chemicals (and thus missing mixture effects), the overall contamination of edibles with xenohormones is largely unknown. The aim of this study was to assess the integrated estrogenic burden of bottled mineral water as model foodstuff and to characterize the potential sources of the estrogenic contamination. Materials, methods, and results  In the present study, we analyzed commercially available mineral water in an in vitro system with the human estrogen receptor alpha and detected estrogenic contamination in 60% of all samples with a maximum activity equivalent to 75.2 ng/l of the natural sex hormone 17β-estradiol. Furthermore, breeding of the molluskan model Potamopyrgus antipodarum in water bottles made of glass and plastic [polyethylene terephthalate (PET)] resulted in an increased reproductive output of snails cultured in PET bottles. This provides first evidence that substances leaching from plastic food packaging materials act as functional estrogens in vivo. Discussion and conclusions  Our results demonstrate a widespread contamination of mineral water with xenoestrogens that partly originates from compounds leaching from the plastic packaging material. These substances possess potent estrogenic activity in vivo in a molluskan sentinel. Overall, the results indicate that a broader range of foodstuff may be contaminated with endocrine disruptors when packed in plastics.     

Organochlorine contaminants in albatrosses and petrels during migration in South Atlantic Ocean

Albatrosses and petrels (Procellariiformes) are migratory oceanic birds of considerable conservational interest. Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were assessed in the subcutaneous fat, liver and muscle of 100 birds belonging to eight species of Procellariiformes collected during their migration period in southern Brazil, one of the most important feeding areas for these species. Although the profiles of PCBs and OCPs were similar among the individuals, with predominance of penta, hexa and heptachlorobiphenyls and p′p-DDE, organochlorine concentrations exhibited a high degree of intra-species variability. The influence of body condition during the migration period in the distribution of organochlorine contaminants was also evaluated, showing that it is a significant factor in the variation and redistribution of these compounds in the tissues of these birds. The intense use of lipid reserves associated to the contamination from organochlorine compounds could be a troubling factor for seabirds with extended breeding periods and that spend most of their lives at sea migrating long distances, such as most of Procellariiformes. Studies on contamination are necessary to improve the knowledge of the threats to these birds and their populations as well as to contribute with information about persistent organic pollutants in the South Atlantic marine environment.     

Industrial plastic on the southern beaches of the Arabian Gulf and the western beaches of the Gulf of Oman

The increasing production and use of plastic in the Arabian Gulf combined with shipping and waste disposal practices, have increased the concentration of plastic particles on the sea's surface and beaches. The objective of this investigation was to provide an assessment of the abundance, distribution, potential sources and significance of industrial plastic on the western beaches of the United Arab Emirates on the Arabian Gulf and on the eastern beaches on the Gulf of Oman. The abundance of stranded plastic pellets was highly uneven. By early 1992 alarming levels of fresh plastic pellets were noticed on the Arabian Gulf beaches of the UAE. Large numbers of 25 kg sacks of white plastic spherules manufactured by (SABIC) in Jubail, Saudi Arabia were washed ashore. When compared to the west coast on the Arabian Gulf, the east coast on the Gulf of Oman exhibited much lower levels of plastic pellets. When compared to other parts of the world, the beaches of the UAE on the Arabian Gulf are considered to be heavily polluted with industrial plastic.     

Coupling between meteorological factors and ambient aerosol load

The coarser (CPM) and respirable (RPM) fractions of aerosol loads collected in a time sequence, during the onset of winter season in Delhi region, were subjected to Principal Component Analysis (15 elemental variables, 39 samples); the absolute mass contributed by each identified source to the CPM and RPM was quantified by using Absolute Principal Component Score (APCS) and Positive Matrix Factorization (PMF) method. Interestingly, the mass contributed by the local crustal source (material) to both fractions manifested undulating periodic behavior, a dominating harmonic corresponding to 24-h period was detected by using Discrete Fourier Transform (DFT). The corresponding harmonics, of varying strengths, were also detected in the recorded meteorological factors: Planetary Boundary Layer (PBL), Surface Level Temperature (T), Surface Level Relative Humidity (RH) and Wind Speed (WS). The analysis of the respective harmonic strength within the CPM, RPM, and meteorological factors suggested that the undulation observed in both size fractions of aerosol load from the local crust was affected by the meteorological factors. The large proportion of undulating loads (CPM and RPM), explained by the dominating harmonic, was fully accounted for by the empirical relation involving the discrete coupling parameters, and the recorded meteorological factors: PBL, T, RH and WS. The analysis suggests that the magnitude and the direction (‘positive’ load increase and ‘negative’ the reverse) of coupled meteorological factors'(s) effect on ambient CPM, RPM load is determined by the phase difference between the harmonic explaining the aerosol fraction's load and the corresponding harmonic present in the respective meteorological factor. The absolute mass contributions arising from the identified sources (APCS and PMF) allowed us to calculate the baseline ambient concentrations of undulating CPM and RPM loads, in the region of this study, affected by meteorological factors only.     

Quantities of bisphenol a leached from plastic waste samples

To quantify the leaching of bisphenol A into water, various samples of plastic waste were cut into small pieces, soaked in water for two weeks at room temperature in the dark, and the concentration of bisphenol A in the water determined by gas chromatography/mass spectrometry (GC/MS). The amount of bisphenol A leached from the plastic wastes ranged from undetectable to 139 micrograms/g. The detection limit was 2 ng/g when 100 g of plastic waste was used. Polyvinyl chloride products yielded the highest concentrations because bisphenol A is used in its manufacture as a stabilizer.     

Hexabromocyclododecanes in soils and plants from a plastic waste treatment area in North China: occurrence,diastereomer- and enantiomer-specific profiles,and metabolization

Plastic waste is a source of organic contaminants such as hexabromocyclododecanes (HBCDs). HBCDs have been found to cause developmental and reproductive toxicity; it is important to investigate the occurrence and metabolization of HBCDs in the soil environments with plastic waste contamination. This work analyzed HBCDs and their metabolites in soil and plant samples collected from Xinle and Dingzhou—the major plastic waste recycling centers in North China. Results showed that total HBCD concentrations in soils followed the order: plastic waste treatment site (11.0–624 ng/g) > roadside (2.96–85.4 ng/g) ≥ farmland (8.69–55.5 ng/g). HBCDs were detected in all the plant samples with total concentrations ranging from 3.47 to 23.4 ng/g. γ-HBCD was the dominant congener in soils, while α-HBCD was preferentially accumulated in plants. Compositions of HBCD isomers in soils and plants were significantly different (P < 0.05) among sampling sites and among plant species. HBCDs in farmland soil and all plant samples exhibited high enantio-selectivity based on the enantiomeric fractions (EFs). Furthermore, metabolites of pentabromocyclododecenes (PBCDEs) were frequently identified in soils, and mono-OH-HBCDs were the most common ones in plants. This study for the first time provides evidences of HBCD contamination in the soil-plant system caused by plastic waste, their stereo-selectivity, and metabolization behavior, improving our understanding of the environmental behavior and fate of HBCDs.     

Evaluation of approaches to calculate critical metal loads for forest ecosystems

This paper evaluates approaches to calculate acceptable loads for metal deposition to forest ecosystems, distinguishing between critical loads, stand-still loads and target loads. We also evaluated the influence of including the biochemical metal cycle on the calculated loads. Differences are illustrated by examples of Cd, Cu, Pb and Zn for a deciduous forest on five major soil types in the Netherlands. Stand-still loads are generally lower than critical loads, which in turn are lower than the target loads indicating that present levels are below critical levels. Uncertainties in the calculated critical loads are mainly determined by the uncertainty in the critical limits and the chemical speciation model. Including the metal cycle has a small effect on the calculated critical loads. Results are discussed in view of the applicability of the critical load concept for metals in future protocols on the reduction in metal emissions.     

Considerations of uncertainty in setting critical loads of acidity of soils: the role of weathering rate determination

The concept of critical loads has been generally accepted throughout Europe, and increasingly in Asian countries and the rest of the world, as providing the data which forms the basis for international negotiations on abatement strategies for emissions of acidifying pollutants. Central to the determination of quantitative critical loads of acidity for forests (and other ecosystems) is the rate at which the minerals in the soil weather or dissolve. Seven methods for determining these rates on a regional basis for the production of critical load maps have been suggested by the official bodies which are responsible for co-ordinating the European critical load mapping efforts. These methods are largely correlations which require a knowledge of the soil parent material and/or the soil mineralogy. The purpose of this paper is to review these weathering rate calculation methods and to assess whether it is currently possible to calculate numerically accurate critical loads for the production of regional critical load maps. A consideration of the data used to generate these methods and comparisons of the weathering rates calculated using various methods leads to the conclusion that at present it is not. Further work is needed to develop and maintain the initial credibility of critical loads both scientifically and as an aid to policy decisions.     

The changing sediment load of the Mekong River

The sediment loads of many of the world's major rivers have changed significantly in recent years due to land-use change, reservoir construction, and other human impacts on their drainage basins. For many rivers, the loads have decreased, whereas for others, they have increased. Such changes can have important implications for both the natural functioning of the system as well as for human exploitation of the river system. This paper considers the evidence for recent changes in the sediment load of the Mekong River. The available data have a number of limitations in terms of both sampling frequency and the period of coverage, but they have been processed to provide a basis for considering the changes in the sediment load of the river over the period extending from the early 1960s to 2002. Although there is evidence of increasing loads at some measuring stations, the overall trends show little evidence of major changes, and the system provides evidence of buffering through storage. As of 2002, the construction of major dams on the headwaters in China appears to have had little impact on the sediment load, although as further larger dams are commissioned, the sediment load of the Mekong can be expected to decrease.