Classification of the sugarcane residues and their characteristics—an environmental assessment of mortar with addition of sugarcane residues

Journal of Material Cycles and Waste Management - The use of agro-residue in resource-limited regions can be a smart way for civil construction to reduce costs, reduce emissions of pollutant gases...     

Effect of γ-Dose rate on Biodegradation of γ-Sterilized Biomedical Polyolefins

The aim of the present study is to study the effect of γ-dose rate on the biodegradation of γ-sterilized polyolefins. Films of isotactic polypropylene, high density polyethylene and ethylene-propylene (EP) copolymer were sterilized under γ-radiation with doses of 10 and 25 kGy. Two different ⁶⁰Co sources were used with dose rate 600 and 780 Gy h⁻¹. Neat and sterilized samples were incubated in compost and fungal culture environments. The changes in functional groups, surface morphology and intrinsic viscosity in polymer chains were characterized by FT-IR spectroscopy, SEM and viscometric measurements, respectively. It was observed that both γ-degradation and biodegradation processes depend on the dose rate of γ-source. It was found that the biodegradation of γ-sterilized polyolefins in composting and microbial culture environments increased with decreasing the γ-dose rate.     

Influence of Processing Additives on the Degradation of Melt-Pressed Films of Poly(ε-Caprolactone) and Poly(Lactic Acid)

Melt-pressed films of polycaprolactone (PCL) and poly(lactic acid) (PLA) with processing additives, CaCO₃, SiO₂, and erucamide, were subjected to pure fungal cultures Aspergillus fumigatus and Penicillium simplicissimum and to composting. The PCL films showed a rapid weight loss with a minor reduction in the molecular weight after 45 days in A. fumigatus. The addition of SiO₂ to PCL increased the rate of (bio)erosion in A. fumigatus and in compost. The use of a slip additive, erucamide, was shown to modify the properties of the film surface without decreasing the rate of bio(erosion). Both the rate of weight loss and the rate of molecular weight reduction of PCL increased with decreasing film thickness. The addition of CaCO₃ to PLA significantly reduced the thermal degradation during processing, but it also reduced the rate of the subsequent (bio)degradation in the pure fungal cultures. PLA without additives and PLA containing SiO₂ exhibited the fastest (bio)degradation, followed by PLA with CaCO₃. The degradation of the PLA films was initially governed by chemical hydrolysis, followed by an acceleration of the weight change and of the molecular weight reduction. PLA film subjected to composting exhibits a rapid decrease in molecular weight, which then remains unchanged during the measurement period, probably because of crystallization.     

Formation of Reactive Gaseous Mercury in the Arctic: Evidence of Oxidation of Hg° to Gas-Phase Hg-II Compounds after Arctic Sunrise

We have measured total gaseous mercury concentrations(Hg°) at Point Barrow, Alaska since September 1998 in aneffort to determine the geographic extent and reaction mechanismof the so-called mercury depletion events (MDE) previouslyreported in the high Arctic at Alert, Canada. Hg° has beensampled now for nearly 2 years at Barrow. In September, 1999, webegan making the first automated measurements of reactive gaseousmercury (RGM) attempted in the Arctic, along with measurements ofHg accumulation in snowpack to determine the fate of the depleted Hg°. During the fall and early winter, Hg°and RGM exhibit only minor variation, Hg° remaining within10% of global background, near 1.6–1.8 ng m^-3. The MDEperiods are quite different, however; within days of Arcticsunrise in January, Hg° exhibits major variations from themean, rapidly dropping as low as 0.05 ng m^-3 and then cyclingback to typical levels, sometimes exceeding global background. These events continue throughout Arctic spring, then end abruptlyfollowing snowmelt, in early June. Prior to Arctic sunrise, RGMremains near detection (<2 pg m^-3), but after sunriseincreases dramatically (to levels as high as 900 pg/m³) insynchrony with the depletion of Hg°. Both phenomenaexhibit a strong diel cycle, in parallel with UV-B. We concludethat MDE's involve rapid in-air oxidation of Hg° to aspecies of RGM by photochemically-driven reactions, probablyinvolving the same reactive bromine and chlorine compoundsinvolved in ozone destruction. Sharp increases in Hg in thesurface snowpack after sunrise coincident with periods of peakRGM suggest surface accumulation of the RGM by dry deposition.     

Assessment of the environmental impact of management measures for the biodegradable fraction of municipal solid waste in São Paulo City

There is increasing concern about landfilling of biodegradable wastes. Therefore, biological treatment processes such as composting and biogasification have been considered as alternative strategies for managing those wastes. In this work, life cycle assessment was employed to compare the environmental impacts of landfilling, composting, and biological treatment of municipal solid waste in S?o Paulo City, Brazil. Energy consumption, recovered resources, and emissions to air and water were quantified and analyzed in terms of their potential contribution to global warming, acidification, and nutrient enrichment impact. The results demonstrated that processes that require high levels of energy consumption, such as wastewater treatment, play an important role in the outcome of environmental impact potentials. It was found that the landfilling of all waste is generally the worst strategy from an environmental point of view. However, significant reductions in the resulting impacts can be accomplished through biogasification and composting of the biodegradable fraction. Regarding composting, the application of a biofilter for gas treatment reduced significantly the gaseous emissions.     

Evaluation of biodegradability of poly(ε-caprolactone)/poly(ethylene terephthalate) blends

The results of an investigation aimed at evaluation of the biodegradability of blends of poly(-caprolactone) (PCL) with poly(ethylene terephthalate) (PET) as the major component are reported. Specimens of the blends, as melt extruded films and/or powders, were submitted to degradation tests under different environmental conditions including full-scale composting, soil burial, bench-scale accelerated aerobic degradation, and exposure to axenic cultures and esterolytic enzymes. Indications have been gained that blending in the melt gives rise to insertion of PCL segments in the PET chain. Copolymers thus attained acted as macromolecular compatibilizers, allowing for a complete miscibility of PCL and PET. The biodegradation detected on the blend samples was, however, well below the values expected from chemical composition and behavior of individual homopolymers under the same environmental conditions. The presence of PET as the major component in PET/PCL blends apparently reduces the propensity of PCL to be degraded, at least in the investigated composition range. The degradation data collected under different environmental conditions indicate that the full-scale composting system is the most efficient among the tested degradation procedures.     

Chronic toxicity of the ‘water-soluble fraction’ of Norman Wells crude oil to juvenile fish

Young rainbow trout were exposed to Norman Wells crude oil for periods as long as 55 d. Mortality was light for the first few days, but it continued throughout exposure with more rapid and increased mortality at the higher exposure levels. The mortality was generally exacerbated by the presence of oil dispersants Corexit 7664 or 9600. Fish surviving the 55-day experiment showed severe fin erosion and apparent ‘flooding’, since mean body water content was increased from about 84% to over 90%. We hypothesize that the oil affected the ability of the fish to regulate their water content.     

How are WEEE doing? A global review of the management of electrical and electronic wastes

This paper presents and critically analyses the current waste electrical and electronic equipment (WEEE) management practices in various countries and regions. Global trends in (i) the quantities and composition of WEEE; and (ii) the various strategies and practices adopted by selected countries to handle, regulate and prevent WEEE are comprehensively examined. The findings indicate that for (i), the quantities of WEEE generated are high and/or on the increase. IT and telecommunications equipment seem to be the dominant WEEE being generated, at least in terms of numbers, in Africa, in the poorer regions of Asia and in Latin/South America. However, the paper contends that the reported figures on quantities of WEEE generated may be grossly underestimated. For (ii), with the notable exception of Europe, many countries seem to be lacking or are slow in initiating, drafting and adopting WEEE regulations. Handling of WEEE in developing countries is typified by high rate of repair and reuse within a largely informal recycling sector. In both developed and developing nations, the landfilling of WEEE is still a concern. It has been established that stockpiling of unwanted electrical and electronic products is common in both the USA and less developed economies. The paper also identifies and discusses four common priority areas for WEEE across the globe, namely: (i) resource depletion; (ii) ethical concerns; (iii) health and environmental issues; and (iv) WEEE takeback strategies. Further, the paper discusses the future perspectives on WEEE generation, treatment, prevention and regulation. Four key conclusions are drawn from this review: global amounts of WEEE will continue unabated for some time due to emergence of new technologies and affordable electronics; informal recycling in developing nations has the potential of making a valuable contribution if their operations can be changed with strict safety standards as a priority; the pace of initiating and enacting WEEE specific legislation is very slow across the globe and in some cases non-existent; and globally, there is need for more accurate and current data on amounts and types of WEEE generated.     

Comparison of the Effect of Plasticizers on PHBV—and Organoclay—Based Biodegradable Polymer Nanocomposites

The aim of this work was to evaluate the effect of different plasticizers on the morphology, crystallization, and mechanical properties of poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV)/organomodified montmorillonite (OMt) nanocomposites. We investigated three different plasticizers: dioctyl phthalate (DOP), a commonly used additive in the polymer industry, and two natural and biodegradable plasticizers: epoxidized soybean oil (ESO) and triethyl citrate (TEC). The nanocomposites with 3 wt% OMt were obtained by melt processing in an internal mixer. The plasticizers were used alone or in combination with clay in a concentration of 10 wt%. X-ray diffraction and scanning electron microscopy results revealed a partially intercalated structure. The degree of crystallinity was higher for all of the samples compared to neat PHBV, although the melting temperature decreased with the use of plasticizers combined with OMt. The impact strength results were dependent on the interaction between the components of the system. Triethyl citrate was the most effective plasticizer due to its more pronounced interaction with the PHBV matrix, which yielded improvements in processing conditions and PHBV’s flexibility and impact properties.     

Design and Characterization of PVA–Methacrylic Acid Based Smart Polymeric System for Controlled Release of Metoprolol

In the present work covalently crosslinked smart polymeric system of hydrogel based on poly vinyl alcohol (PVA) and methacrylic acid (MA) was designed by free radical polymerization with different compositions using glyoxal (40 % water solution) as crosslinker. It was observed that swelling of hydrogel had a pronounced enhancing effect on increasing the concentration of MA due to availability of more ionized carboxylic groups of MA but produced an opposite effect on increasing the concentration of glyoxal owing to less porous structure. As far as PVA is concerned, swelling did not show significant effect on increasing the concentration of PVA. Hydrophilic polymer PVA rich in hydroxyl group pertained to be highly interactive with water. It was examined that the release of metoprolol tartrate decreased with increased concentration of glyoxal, but increased with increase in concentration of MA. PVA/MA hydrogel was characterized by Fourier transform infrared spectroscopy and X-ray diffraction to study the structure and crystallinity of hydrogel respectively. Morphology was studied through scanning electron microscopy. Furthermore differential scanning calorimetry and thermogravimetric analysis were also performed to characterize thermal stability. It may be concluded that the mechanism of drug release was mainly non-Fickian diffusion.     

Electrosynthesis of κ-Carrageenan Complexes with Gelatin

Electrosynthesis at pH 9, 12, and 11 of -carrageenan–gelatin complexes from electrolytes containing the components at proportions varying from 1:5 to 5:1 provided complexes in the composition varying in a range from 1:10 to 1:1.8. Components were bound mainly electrostatically, although partial insolubility of complexes in 7 M aqueous urea pointed to a part of the complexes bound covalently. None of the performed tests except solubility could confirm formation of covalent complexes. The complexation of -carrageenan to gelatin significantly increased the thermal stability of carrageenan, whereas the thermal stability of gelatin increased rather insignificantly.     

Deterioration of Polyamideamine–Epichlorohydrin (PAE) in Aqueous Solutions During Storage: Structural Changes of PAE

Structural changes of polyamideamine–epichlorohydrin (PAE) in solution during storage at 4 °C and pH 4.2–4.5 for up to 8.9 years were studied by ¹H- and ¹³C-NMR analyses, colloidal titration and others. NMR signals due to 3-hydroxy-azetidinium groups of PAE decreased during storage, and correspondingly 2, 3-dihydroxypropyl groups were formed by the ring opening. The content of 3-hydroxy-azetidinium groups in PAE determined by ¹H-NMR were similar to that determined by the colloidal titration, although the former was higher than the latter. About 50% of the 3-hydroxy-azetidinium groups present in the fresh PAE were lost during storage for 8.9 years. Furthermore, ¹³C-NMR analysis revealed that significant depolymerization of polyamideamine chains occurred by hydrolysis of the amide linkages during storage. Rough evaluation of number average degree of polymerization (DPn) of the amideamine repeating unit showed that the DPn decreased from 12 to 2 during storage for 8.9 years.     

Treatment of organic-contaminated industrial wastes using cement-based stabilization/solidification—I. Microstructural analysis of cement-organic interactions

The major deficiencies in cement-based stabilization/solidification (S/S) processes are their inability to treat inorganic wastes contaminated with organic material or organic wastes. In general, organic compounds are poorly retained in a cement matrix and frequently have a detrimental, poorly understood, effect upon cement hydration and strength development. These interactions need to be understood as fully as possible, however, if S/S processes are to be developed in ways which will assure the long-term integrity of the resultant products.The work presented in this paper investigates some fundamental aspects of the interactions of two organic compounds, 3-chlorophenol and chloronaphthalene, with a cement matrix. Phenolic compounds have previously been shown to have a detrimental effect upon the macrostructural properties of ordinary Portland cement (OPC), for example, the strength, setting rate and leachability (Montgomery et al. 1988). Microstructural studies in this work have shown that 3-chlorophenol inhibits the hydration of tricalcium silicate (C₃S in cement chemists' notation), with up to 90% of the C₃S remaining after 28 days for highly dosed 3-chlorophenol/OPC samples. The formation of ettringite was found to be increased by the presence of 3-chlorophenol and its conversion to monosulphate inhibited. Scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) analysis of the samples showed that 3-chlorophenol crystallized in the cement matrix to form discrete crystals containing calcium and phenol. In contrast, chloronaphthalene had no observable effect on hydration reactions. In a subsequent paper, detailed studies will be presented showing how these deleterious effects can be minimized by the use of organophilic clays as a pre-solidification adsorbent.     

PHB/V in Extrusion Coating of Paper and Paperboard—Study of Functional Properties. Part II

Extrusion coating experiments were carried out in the pilot line at Tampere University of Technology (Institute of Paper Converting). Commercially produced 3-hydroxybutyrate/3-hydroxyvalerate copolymer, commercial Finnish paper, and paperboard qualities were utilized as substrates. Functional properties, such as heat-sealing and hot-tack properties, pinhole density, and water vapor transmission rate were determined. PHB/V coatings exhibited approximately four–six times higher water vapor transmission rates (WVTR) than the corresponding LDPE coatings. The incorporation of wax or tall oil rosin into PHB/V improved its water vapor barrier. Curling of PHB/V was reduced by the addition of wax or tall oil rosin into the base polymer. PHB/V provided good heat-sealing characteristics at rather high sealing temperatures. Pinhole density was substantially reduced by using higher molecular weight PHB/V and by incorporating plasticizer into PHB/V.     

Influence of regulation on the productivity of waste utilities. What can we learn with the Portuguese experience?

This paper examines the merits and the perverse effects of quality of service regulation in the performance of urban waste services when implemented alone and compares the performance of different economic regulatory methods. By means of a productivity analysis, we investigate the influence of a five-year period of regulation on the performance of Portuguese urban waste utilities using an unbalanced panel data for the period 2001-2008. Different non-parametric methods were applied to estimate the productivity change, all leading to similar outcomes. We observed a tendency of productivity decline in the urban waste utilities and concluded that in spite of the unequivocal improvements in the quality of service induced by sunshine regulation, more should be done as far as economic regulation is concerned. We also found that the use of sunshine regulation together with low incentive economic regulatory methods is not positive, leading to overinvestment rather than to value for money.     

The in situ treatment of PFAS within porewater at the air–water interface of a PFAS source zone

The treatment of per- and polyfluoroalkyl substances (PFAS) within groundwater is an emerging topic, with various technologies being researched and tested. Currently, PFAS-impacted groundwater is typically treated ex situ using sorptive media such as activated carbon and ion exchange resin. Proven in situ remedial approaches for groundwater have been limited to colloidal activated carbon (CAC) injected into aquifers downgradient of the source zones. However, treatment of groundwater within the source zones has not been shown to be feasible to date. This study evaluated the use of CAC to treat dissolved PFAS at the air–water interface within the PFAS source zone. Studies have shown that PFAS tends to preferentially accumulate at the air–water interface due to the chemical properties of the various PFAS. This accumulation can act as a long-term source for PFAS, thus making downgradient treatment of groundwater a long-term requirement. A solution of CAC was injected at the air–water interface within the source zone at a site with PFAS contamination using direct push technology. A dense injection grid that targeted the interface between the air and groundwater was used to deliver the CAC. Concentrations of PFAS within the porewater and groundwater were collected using a series of nine lysimeters installed within the vadose and saturated water columns. A total of six PFAS were detected in the porewater and groundwater including perfluorobutanoic acid (PFBA), perfluoropentanoic acid (PFPeA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorooctanoic acid (PFOA), and perfluorononanoic acid (PFNA). Detectable concentrations of PFAS within the pore and groundwater before treatment ranged from values greater than 300 µg/L for PFPeA to less than 3 µg/L for PFNA. Following the injection of the CAC, monitoring of the porewater and groundwater for PFAS was conducted approximately 3, 6, 9, 12, and 18 months postinjection. The results indicated that the PFAS within the porewater and groundwater at and near the air–water interface was effectively attenuated over the 1.5-year monitoring program, with PFAS concentrations being below the method detection limits of approximately 10 ng/L, with the exception of PFPeA, which was detected within the porewater during the 18-month sampling event at concentrations of up to 55 ng/L. PFPeA is a five carbon-chained PFAS that has been shown to have a lower affinity for sorption onto activated carbon compared to the longer carbon-chained PFAS such as PFOA. Examination of aquifer cores in the zone of injection indicated that the total organic carbon concentration of the aquifer increased by five orders of magnitude postinjection, with 97% of the samples collected within the target injection area containing activated carbon, indicating that the CAC was successfully delivered into the source zone.     

A Study of the Photocatalytic Oxidation of Humic Acid on Anatase and Mixed-phase Anatase–Rutile TiO2 Nanoparticles

In this study, slurry photocatalytic oxidation process was investigated for natural organic matter removal from aqueous humic acid solutions by using different titanium dioxide (TiO₂) under UV-A irradiation. Bench scale experimental studies were conducted at different humic acid concentration at the range of 10–50 mg/L and different pH. Anatase and mixed-phase anatase–rutile TiO₂ nano particles used in the photocatalytic reactor. The results were evaluated in terms of the parameters that are specific to organic matter content such as dissolved organic carbon concentration, ultraviolet absorbance at 254 nm (UV₂₅₄), specific ultaviolet absorbance at 254 nm, and color (VIS₄₀₀). It was observed that increasing humic acid concentration decreases photocatalytic degradation efficiency. The reactivity of the mixed-phase anatase–rutile (Degussa P-25) TiO₂ was greater than individual anatase particles and the highest efficiency was observed at pH 3 for anatase TiO₂.     

University students’ awareness of e-waste and its disposal practices in Pakistan: a construction of the conceptual framework

Journal of Material Cycles and Waste Management - Pakistan is among the few countries generating and receiving enormous e-waste, which posits a threat to its&nbsp;future generations. A...