Quantification of landfill emissions to air: a case study of the Ano Liosia landfill site in the greater Athens area.

Fugitive pollutant emissions from municipal solid waste landfills have the potential to cause annoyance and health impacts in the surrounding residential areas. The overall objective of this research was to perform an assessment of fugitive pollutant emissions and a dispersion analysis downwind of a specific landfill site. The study was performed at the closed Ano Liosia landfill site which is located in the greater Athens area. The human exposure from priority to health-risk pollutants emitted from landfill, such as vinyl chloride and benzene, was estimated by the landfill gas emission LandGEM 2.01 software combined with the atmospheric long-term dispersion model ISC3-LT. The emission and meteorological conditions under which the models were applied referred to the worst-case scenario. This scenario was used for the evaluation of the maximum human exposure assessed beyond the Ano Liosia landfill towards the residential areas. The above scenario provides the minimum downwind distance of the health-risk zone which is calculated to be equal to 1.5 km from the landfill. Within this distance the assessed air pollutant concentration for several air pollutants was significantly above the World Health Organization reference lifetime exposure health criteria. Finally, the applied methodology was used in the Ano Liosia landfill, where atmospheric concentrations of pollutants measured in the field were compared with model predictions.     

The effect of dust emissions from open storage piles to particle ambient concentration and human exposure

The current study focus on the determination of dust emissions from piles in open storage yards of a municipal solid waste (MSW) composting site and the subsequent atmospheric dust dispersion. The ISC3-ST (Industrial Source Complex Version 3 – Short Term) model was used for the evaluation of the PM₁₀ ambient concentrations associated with the dispersion of MSW compost dust emissions in air. Dust emission rates were calculated using the United States Environmental Protection Agency proposed dust resuspension formulation from open storage piles using local meteorological data. The dispersion modelling results on the spatial distribution of PM₁₀ source depletion showed that the maximum concentrations were observed at a distance 25–75 m downwind of the piles in the prevailing wind direction. Sensitivity calculations were performed also to reveal the effect of the compost pile height, the friction velocity and the receptor height on the ambient PM₁₀ concentration. It was observed that PM₁₀ concentrations (downwind in the prevailing wind direction) increased with increasing the friction velocity, increasing the pile height (for distances greater than 125 m from the source) and decreasing the receptor height (for distances greater than 125 m from the source). Furthermore, the results of ISC3-ST were analysed with the ExDoM (Exposure Dose Model) human exposure model. The ExDoM is a model for calculating the human exposure and the deposition dose, clearance, and finally retention of aerosol particles in the human respiratory tract (RT). PM₁₀ concentration at the composting site was calculated as the sum of the concentration from compost pile dust resuspension and the background concentration. It was found that the exposure to PM₁₀ and deposited lung dose for an adult Caucasian male who is not working at the composting site is less by 20–74% and 29–84%, respectively, compared to those for a worker exposed to PM concentrations at the composting site.     

Effects of Natural and Artificial Weathering on the Physical Properties of Recycled Poly(ethylene terephthalate)

In accelerated weathering tests, specimens are exposed to higher radiation intensity, temperature and humidity than is likely under natural weathering in order to achieve rapid degradation of the polymer in a convenient short time. In the current work, a correlation between the two environments is attempted so that a prediction of lifetimes in the natural environment can be achieved. During aging, surface flaws are created due to the chain scission process. This is initiated by the absorption of ultra-violet light and directly affects visual appearance and impact strength. After natural weathering, the material shows only plastic deformation in an impact test. However, after artificial weathering to 5000 h of UV exposure, there is a decrease of 85% in impact strength. Colour change occurs at a high rate in the early stages of UV exposure. Beyond 2000 h of exposure, the colour change approaches a steady state and a correlation between the changes under natural and artificial weathering becomes apparent for a potential prediction of lifetimes. From the analysis including the specular component (SCI), taking surface roughening into account, 1 year under natural weathering was found to be equivalent to 25 days under accelerated weathering.     

Study of the reuse of treated wastewater on waste container washing vehicles

The wheelie bins for the collection of municipal solid waste (MSW) shall be periodically washed. This operation is usually carried out by specific vehicles which consume about 5000 L of water per day. Wastewater derived from bins washing is usually stored on the same vehicle and then discharged and treated in a municipal WWTP. This paper presents a study performed to evaluate the reuse of the wastewater collected from bins washing after it has been treated in a small plant mounted on the vehicle; the advantage of such a system would be the reduction of both vehicle dimension and water consumption. The main results obtained by coagulation–flocculation tests performed on two wastewater samples are presented. The addition of 2 mL/L of an aqueous solution of aluminum polychloride (18% w/w), about 35 mL/L of an aqueous solution of CaO (4% w/w) and 25 mL/L of an aqueous solution of an anionic polyelectrolyte (1‰ w/w) can significantly reduce turbidity and COD in treated water (to about 99% and 42%, respectively); the concomitant increase of UV transmittance at 254 nm (up to 15%) enables UV disinfection application by a series of two ordinary UV lamps. Much higher UV transmittance values (even higher than 80%) can be obtained by dosing powdered activated carbon, which also results in a greater removal of COD.     

Performance evaluation of material separation from spent fluorescent lamps using the thermal end-cutting method

The recovery of valuable materials such as aluminum, phosphor powder, and glass from spent fluorescent lamps (SFLs) is part of the overall recycling process of lamps. In the end-cutting process, an SFL is separated into a base cap and a glass part using thermal shock caused by the temperature difference between the heating unit and the cooling unit. The separation efficiency of the end-cutting system is estimated by measuring the mass of the parts of the SFL. The optimum condition of the end-cutting process with thermal shock was determined to have a temperature difference of 600 °C and moving speed of 2 cm/s. At optimum conditions, the separation efficiency of glass and the end cap from an SFL using the end-cutting method is estimated to be more than about 97 %. In an air injection system, however, the separation efficiency of phosphor powder from glass is less than 50 %. Separation efficiency in the end-cutting system is increased by decreasing the moving speed of the SFL and increasing the temperature difference between the heating unit and the cooling unit. From the results of experiments, it was found that the end-cutting unit has very high performance because the overall separation efficiency is more than 95 %.     

Atmospheric Levels of Nitrogen Oxides at a Greek Oil Refinery Compared with the Urban Measurements in Athens

Oil refining is among the industrial activities that emit considerable amounts of air pollutants into the atmosphere. Nitrogen oxides are important air pollutants that are emitted by oil refineries as products of combustion processes. The ambient air concentrations of nitrogen oxide (NO) and nitrogen dioxide (NO₂) were monitored continuously at a site close to an oil refinery, near the city of Corinth in Greece, during autumn 1997 together with the main meteorological parameters. The contribution of the oil refinery to the measured atmospheric levels of nitrogen oxides was estimated. The ambient air concentration of nitrogen oxides in the area surrounding the oil refinery were generally lower than the ambient air concentrations in the urban area of Athens in Greece, and the NO₂ levels were always below the existing air quality standards. The influence of the refinery emitted NO_x in the photochemical production of ozone seems to be more important in terms of human and vegetation exposure given the high ozone backgrounds measured in the area.     

Characterization and recovery of mercury from spent fluorescent lamps

Fluorescent lamps rely on mercury as the source of ultraviolet radiation for the production of visible light. Partitioning of mercury among vapor phase, loose phosphor powders produced during breaking and washing steps, glass matrices, phosphor powders attached on the glass and aluminum end caps was examined from simulated laboratory lamp recycling tests for different types of spent and new fluorescent lamps. Mercury concentrations in lamp glasses taken from commercial lamp recyclers were also analyzed for comparison with the simulated results of spent and new lamps of different types. The mercury content of the glass from spent lamps was highly variable depending on the lamp type and manufacturer; the median values of the mercury concentration in glasses for spent 26- (T8) and 38-mm (T12) diameter fluorescent lamps were approximately 30 and 45 microg/g, respectively. The average mercury concentration of samples taken from recycler A was 29.6 microg/g, which was about 64% of median value measured from the spent T12 lamps. Over 94% of total mercury in lamps remained either as a component of phosphor powders attached inside the lamp or in glass matrices. New T12 lamps had a higher partitioning percentage of elemental mercury in the vapor phase (0.17%) than spent T12 lamps (0.04%), while spent lamps had higher partitioning percentages of mercury resided on end-caps and phosphor powders detached from the breaking and washing steps. The TCLP values of simulated all lamp-glasses and samples obtained from recyclers were higher than the limit of LDR standard (0.025 mg/L). After investigating acid treatment and high temperature treatment as mercury reclamation techniques, it was found that heating provided the most effective mercury capture. Although the initial mercury concentrations of individual sample were different, the mercury concentrations after 1 h exposure at 100 degrees C were below 4 mug/g for all samples (i.e., <1% remaining). Therefore, it is recommended that heating be used for recovering mercury from spent fluorescent lamps.     

Waste rechargeable electric lamps: characterisation and recovery of lead from their lead-acid batteries

Electrical electronics constitute a significant quantity of municipal solid wastes which are discarded after use in open dumpsites especially in the developing countries. The aim of this study was to characterise the material and chemical components, evaluate current management practices and investigate recovery of lead from battery electrodes (BEs) of waste rechargeable electric lamps (RLs). Twenty-six waste RLs of different models were sampled in Nigeria and characterised. Their BEs were analysed for Pb, Cr, Mn, Cu, Zn, Ni and Fe after acid digestion. Questionnaires were distributed to unselected respondents to assess usage and disposal of the lamps. Reaction of citric acid solutions with Pb in the presence of H₂O₂ was used for the recovery of Pb. 69 % of the respondents disposed their waste RLs in open dumpsites. The mean ± SD concentrations of Pb, Cr, Mn, Cu, Zn, Ni and Fe in the BEs were 600 ± 0.2 g/kg, 65.4 ± 40 mg/kg, 5.05 ± 4.0 mg/kg, 6.81 ± 5.0 mg/kg, 5.98 ± 3.0 mg/kg, 50.0 ± 30 mg/kg and 40.2 ± 35 mg/kg, respectively. The results show that the batteries are lead-acid batteries which require management. At the optimal conditions of S/L = 0.14, temperature = 20 °C and leaching time = 5 h, about 95 % Pb was recovered in form of lead citrate from the battery. High recovery of Pb is possible with simple and environment-friendly reactions.     

Hydrothermal treatment and characterization of model food garbage,focusing on the effect of additional foreign matter on internal temperature,pressure and products

Hydrothermal treatment of model food garbage focusing on the effects of additional foreign matter has been performed in subcritical conditions as a pretreatment for the next step, i.e., the bio-processing and production of liquid feed or fertilizer. Using the hydrothermal technique, we studied the temporal change in internal temperature and pressure in a reactor on the elapsed heating time to check the equipment safety in terms of temperature and pressure. The gaseous and water-soluble liquid was also characterized to investigate the feasibility of retrieving valuable chemicals and emitting environmentally hazardous substances. From the changes in the internal temperature and pressure curve, the maximum temperature and pressure were 196 °C and 1.42 MPa for 30-min elapsed heating time, which was below the predefined temperature limits of 200 °C and pressure of 1.55 MPa. No such irregular behavior was observed in the temperature and pressure curve except that it was a little different for the foreign matter detergent, which also was within the limits. The qualitative and quantitative analysis of end products showed that the emitted malodorous substances and chemicals were further below the threshold levels for Japan.     

Emissions from mesoscale in situ oil fires: the mobile 1991 experiments

A series of 14 mesoscale burns were conducted in 1991 to study various aspects of oil burning in situ. Extensive sampling and monitoring of these burns were conducted to determine the emissions. This was done at two downwind ground stations, one upwind ground station and in the smoke plume using a blimp and a remote-controlled helicopter. Particulate samples in air were taken and analyzed for polycyclic aromatic hydrocarbons (PAHs). PAHs were found to be lower in the soot than in the starting oil. Metals in the oil were found concentrated in the residue and could not be measured in soot samples using conventional industrial hygiene sampling techniques. Particulates in the air were measured by several means and found to be greater than recommended exposure levels only up to 150 m downwind at ground level. Combustion gases including carbon dioxide, sulphur dioxide and carbon monoxide did not reach exposure level maximums. These gases were emitted over a broad area around the fire and are not directly associated with the plume trajectory. Volatile organic compound (VOCs) emissions are extensive from fires, but the levels are less than those emitted from a non-burning test spill. Over 50 compounds were identified and quantified, several at possible levels of concern up to 200 m downwind. Water under the burns was analyzed; no analytes of concern could be found at the detection levels of the methods. The burn residue was analyzed for the same compounds as the air particulate samples. The residue contained elevated amounts of metals. PAHs were at a lower concentration in the residue than in the starting oil, however there is a slight differential concentration increase in some higher molecular weight species. Overall, indications from these mesoscale trials are that emissions from in situ burning are low in comparison to other sources of emissions and result in concentrations of air contaminants that are below exposure limits beyond 500 m downwind.     

SETTING DIOXIN EMISSION LIMITS FOR MSW INCINERATORS: A MULTIMEDIA EXPOSURE ASSESSMENT FRAMEWORK

Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are emitted in trace amounts from municipal solid waste (MSW) incinerators. The exposure to PCDD/Fs experienced by an individual is dominated by the food chain pathway, which accounts for over 98% of the total uptake. Defining a target daily intake (the World Health Organization TDI of 10 pg I-TEQ kg.bw⁻¹day⁻¹) exposure assessment algorithms were then applied to arrive at the corresponding PCDD/F levels in air, soil, plants, food products, etc., which would allow the target intake to be met while retaining the balance of intake between the various exposure pathways. These concentrations were converted to an ambient air concentration of PCDD/Fs and ultimately, by defining criteria for acceptability, to a guide value for PCDD/F concentration in emissions from the MSW incinerator. This strategy was applied to PCDD/F emissions from MSW incinerators of various sizes against two illustrative criteria for acceptability: an “insignificant” release and a threshold above which the release may require further assessment for environmental effects and for control. Using the criteria developed in this paper, the current PCDD/F emission limit of 0.1 ng I-TEQ m⁻³results in an emission that is classed as “insignificant” for all plant sizes. However, higher emission concentrations can also be accommodated below the threshold for further assessment and control.     

A Geochemical Multi-Methodological Approach in Hazard Assessment of CO2-Rich Gas Emissions at Mt. Amiata Volcano (Tuscany, Central Italy)

The present work aims to assess the hazard for human health related to CO₂ anomalous concentrations in air emitted from dry gas vents located in the NE area of Mt. Amiata volcano (Tuscany, central Italy). A geochemical multi-methodological approach is adopted to determine the composition and the flux rate of the gas discharges in order to establish (1) the origin of the gas vents and (2) the behaviour of the discharged gases in the areas surrounding the emission sites. The gas vents are hosted within sub-circular morphological depressions (??～?10–30 m), which likely originated by the collapse of cavities formed at shallow depth in the ground by dissolution of Triassic anhydrite formations and recent travertine deposits. CaCO₃ and CaSO₄ dissolution is mainly related to the underground circulation of CO₂-rich fluids whose hydrological pattern is regulated by local and regional tectonics. The CO₂-rich (up to 996,070 μmol/mol) gases tend to accumulate within the topographic lows, thus creating a sort of CO₂ ponds, and the knowledge of their evolution in time and space is important to evaluate the related hazard. Consequently, a conceptual model of CO₂ diffusion in air is developed to understand the dynamic of the CO₂ accumulation/dispersion process based on (1) a 24-h continuous measurement of the CO₂ flux from one of the main emission sites and (2) the recording of the main meteoric parameters, i.e. air temperature, wind direction and speed to check their influence. The results indicate that the threshold of CO₂ concentrations considered dangerous for the human health is frequently overcome. Moreover, when meteoric conditions, i.e. low wind and cloudy weather, did not allow a rapid dispersion of the gas phase emitted from the dry vents, CO₂-rich clouds periodically overflowed the morphological depressions for several tens of meters without any significant mixing with air. On the basis of these considerations, the monitoring of the output rate from the main gas emissions, combined with the continuous control of the local meteorological parameters, may be considered an efficient procedure to mitigate the CO₂ hazard deriving from dry gas vents. An improvement of the protocol can be achieved in case of installations of CO₂ sensors located in the most sensitive areas and connected to a telemetry system able to transmit the data in real time to the closest Civil Defence centre. The CO₂ degassing sites can also represent a tourist attraction after the installation of suitable metallic fences and a proper campaign of information about these natural phenomena.     

Ex situ treatment of MTBE‐containing groundwater by a UV peroxide system

This article describes the design, implementation, and operating results for an ex situ ultraviolet/hydrogen peroxide (UVP) system to treat methyl tert‐butyl ether (MTBE) in extracted groundwater. The UVP modification was designed to reduce the operation and maintenance costs of an existing groundwater pump‐and‐treat treatment system that relied on air stripping and carbon adsorption. The UVP system is relatively inexpensive and can easily be scaled to cope with different groundwater extraction rates up to 80 gpm by adding UV lamps in series or in parallel at the higher groundwater extraction rates. The MTBE concentration in the effluent from the UVP system to the carbon vessels decreased from an average of 590 μg/L to approximately 2 μg/L on average over 33 months of operation of the UVP. Incorporation of this UVP modification as a second‐stage treatment to the groundwater pump‐and‐treat/soil vapor extraction system, after the air stripper and prior to the carbon vessels, significantly increased the usable life of the carbon (from two months previously to about two years after installation) and completely resolved the issue of frequent MTBE breakthroughs of the carbon that had plagued the remediation system since its inception. © 2006 Wiley Periodicals, Inc.     

Physical Properties, Photo- and Bio-degradation of Baked Foams Based on Cassava Starch, Sugarcane Bagasse Fibers and Montmorillonite

The objectives of this work were to develop biodegradable trays from cassava starch, sugarcane fibers and Na-montmorillonite (Na-MMT) using a baking process and to study the effects of these components on the physical properties, photo- and bio-degradation of the trays. The sample F20 (produced with 20 g fiber/100 g formulation) showed the maximum yield production (100 %). All formulations resulted in well-shaped trays with densities between 0.1941 and 0.2966 g/cm³. The addition of fibers and Na-MMT resulted in less dense and less rigid trays compared to control samples (only starch). The studied processing conditions resulted in good nanoclay dispersion, leading to the formation of an exfoliated structure. The evaluation of the photo-degradation stability of the trays under UV exposure for 336 h showed that a sample produced with a specific combination of fiber and nanoclay (20 g fiber and 5 g nanoclay/100 g formulation) had the highest loss in stress at break (91 %). Biodegradation assays showed that Control trays (starch) and F20 (20 g fiber/100 g formulation) lost a greater percentage of their weight after 90 days of incubation in soil, with losses of up to 85.50 and 82.70 %, respectively.     

Removal of Reactive Blue 19 dye from synthetic wastewater using UV/H2O2 and UV/Cl advanced oxidation processes

The textile and dyeing industries are among the largest water-consuming and polluting industries in the world. The most important feature of the textile dyeing industry wastewater is its color, due to the use of colored materials. Most of these dye compounds are resistant to conventional purification methods and their biodegradation is very low through secondary purification processes, resulting in incomplete removal. Therefore, selecting the optimal method to remove these color compounds is essential. In this study, we studied the removal of an organic dye contaminant (Reactive Blue dye 19 [RB19]) using advanced oxidation processes (AOPs). For this purpose, ultraviolet (UV) mercury lamps with a wavelength of 254 nm and a voltage of W16 inside a reactor were used as an energy source. The experiments were performed in a collimated beam reactor inside a dark chamber. Two oxidizers, sodium hypochlorite (NaOCl) and hydrogen peroxide (H₂O₂), were used to remove RB19 from the artificial sewage stream. Removal of RB19 with a concentration of 20 mg/L with variable pH (5, 7, and 9), oxidant concentrations (5, 10, and 20 mg/L), and time (5, 10, 15, and 30 min) were investigated during the processes of photolysis, chemical oxidation (by H₂O₂ and NaOCl), and UV/NaOCl and UV/H₂O₂ AOPs. The photolysis process did not remove the RB19. The highest removal efficiencies of RB19 by chemical oxidation processes with NaOCl and H₂O₂, UV/NaOCl, and UV/H₂O₂ at optimal conditions (pH = 5, [oxidant] = 20 mg/L, RB19 = 20 mg/L, and radiation intensity of 1005 mJ/cm²) were 64.49%, 0.88%, 99.7%, and 13.31%, respectively. These results indicate that the hydroxyl radical was produced, under optimum conditions, more in the acidic medium; thus, the RB19 removal efficiency was higher in the acidic medium. The combination of UV rays with oxidants resulted in the production of more hydroxyl radicals and increased removal efficiency.     

Dose Assessment for Process Water Tunnels at Hanford Site

The RESRAD‐BUILD and RESRAD computer codes were used for dose assessment of the 105‐C Process Water Tunnels at the Hanford Site. The evaluation assessed three different exposure scenarios: recreational use, tunnel maintenance worker, and residential use. The recreationist and maintenance worker scenarios were evaluated by using RESRAD‐BUILD, a computer model for analyzing the radiological doses resulting from remediation and occupancy of structures contaminated with radioactive material. The recreationist was assumed to use the tunnels as an overnight shelter for eight hours per day for one week. The maintenance worker was assumed to spend 20 hours per year working in the the tunnel. Six exposure pathways were considered for both scenarios in dose assessment. The gradual removal of surface contamination over time and ingrowth of decay products were considered in calculating the dose at different times. The maximum dose would occur immediately after the release and was estimated to be 1.9 mrem/yr for the recreationist and 0.9 mrem/yr for the maintenance worker. The residential scenario was evaluated by using the probabilistic RESRAD code. It was assumed that total activity from the tunnels would be brought into the near‐surface layer by future human activities. Eight exposure pathways were considered. The maximum yearly dose for this very unlikely scenario would occur immediately after the release and was less than 4 mrem/yr for the maximally exposed individual. The assessment demonstrates that both codes are suitable for nuclear facility decontamination and decommissioning sites, where buildings and structures with residual radioactivity must be evaluated to facilitate property transfer or release.     

Waste management health risk assessment: A case study of a solid waste landfill in South Italy

An integrated risk assessment study has been performed in an area within 5 km from a landfill that accepts non hazardous waste. The risk assessment was based on measured emissions and maximum chronic population exposure, for both children and adults, to contaminated air, some foods and soil. The toxic effects assessed were limited to the main known carcinogenic compounds emitted from landfills coming both from landfill gas torch combustion (e.g., dioxins, furans and polycyclic aromatic hydrocarbons, PAHs) and from diffusive emissions (vinyl chloride monomer, VCM). Risk assessment has been performed both for carcinogenic and non-carcinogenic effects. Results indicate that cancer and non-cancer effects risk (hazard index, HI) are largely below the values accepted from the main international agencies (e.g., WHO, US EPA) and national legislation (D.Lgs. 152/2006 and D.Lgs. 4/2008).     

Processes for water reclamation

Water treatments fall into two broad classes; those that remove or destroy specific classes of pollutants, i.e. color, metal ions, hardness, sediment, bacteria, etc., and those that remove water from nearly all of the pollutants. The first class includes sedimentation, biological treatment by microbes, chemical precipitation, adsorption on active carbon or ion exchange resins, and disinfection. The second class includes distillation, freezing and reverse osmosis (RO). The first class are the least expensive in terms of energy and have a long history of successful use on a large scale to reclaim water containing sewage. Most of the second group are energy intensive and have been used primarily on a moderate scale. All processes, except disinfection, leave a residual sludge or brine that contains a substantial quantity of water.Many of the problems of treating waste water for reuse on Earth stem from the fact that waste water carries pathogenic organisms from one location to another and may spread disease over long distances. In a closed group, such as in a Space Station, there are so many other routes for transfer of microorganisms, i.e. in the air, on surfaces, by hand-to-mouth, that undue emphasis on disinfection of water is inappropriate. Successful examples of water reuse on Earth are reviewed in terms of their possible application in space.     

Synthesis and Characterization of Chitosan-Grafted-Poly(2-Hydroxyaniline) Microstructures for Water Decontamination

Chitosan as a biopolymer, biodegradable, safe, non-toxic and widely abundant in nature was grafted with poly(2-hydroxyaniline) (P2-HA) through aqueous chemical oxidative copolymerization using ammonium persulphate in acetic acid medium. The grafting conditions were studied by varying grafting parameters. The effect of oxidant, 2-hydroxyaniline (2-HA) and acetic acid concentrations on the rate of copolymerization was studied. The synthesized graft characterized using UV–Vis, FTIR, TGA, XRD, and scanning electron microscope and compared with chitosan and P2-HA. The grafting enhances the thermal properties of chitosan. The effect of temperature on the rate of grafting copolymerization reaction was studied. The apparent activation energy (Ea) of the copolymerization reaction found to be 21.1116 kJ/mol. Also, ΔH^* and ΔS^*, were calculated and found to 22.8630 kJ/mol and ?109.4290 J/mol K respectively. The mechanism of the grafting copolymerization reaction discussed. Chitosan, P2-HA and chitosan-graft-P2-HA used for the removal of Cr, Fe, Mn, Cu and Zn divalent ions from a contaminated water samples. The adsorption isotherm parameters are given.     

Compatibilization Improves Performance of Biodegradable Biopolymer Composites Without Affecting UV Weathering Characteristics

With growing interest in the use of eco-friendly composite materials, biodegradable polymers and composites from renewable resources are gaining popularity for use in commercial applications. However, the long-term performance of these composites and the effect of compatibilization on their weathering characteristics are unknown. In this study, five types of biodegradable biopolymer/wood fiber (WF) composites were compatibilized with maleic anhydride (MA), and the effect of accelerated UV weathering on their performance was evaluated against composites without MA and neat biopolymers. The composite samples were prepared with 30 wt% wood fiber and one of the five biodegradable biobased polymer: poly(lactic) acid (PLA), polyhydroxybutyrate (PHB), poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), Bioflex (PLA blend), or Solanyl (starch based). Neat and composite samples were UV weathered for 2000 h (hours), and characterized for morphological, physical, thermal, and mechanical properties before and after weathering. Compared to composites without MA, composites containing MA grafted polymers exhibited improved properties due to increased interfacial adhesion between the fiber and matrix. Upon accelerated weathering, thermal and mechanical properties of 70% of the samples substantially decreased. Surfaces of all the samples were roughened, and drastic color changes were observed. Water absorption of all the samples increased after weathering exposure. Even though the compatibilization is shown to improve composite properties before weathering, it did not affect weathering of samples, as there were no considerable differences in properties exhibited by the composites with MA and without MA after weathering. The results suggest that compatibilization improves properties of biodegradable biobased composites without affecting its UV degradation properties.