A holistic reverse logistics planning framework for end-of-life PV panel collection system design.

Photovoltaic (PV) technologies are critical for sustainable energy supply, climate change mitigation, and energy security with lower environmental impact compared to other generation alternatives. Despite the environmental benefits of PV technologies, one of these major downsides is the growing concern over the environmental impact due to risks associated with improper waste handling and disposal of decommissioned PV panels. As a result, there are strong incentives for PV panel recycling to recover valuable resources and mitigate risks caused by hazardous substances. This study proposes a reverse logistical planning framework for collecting end-of-life PV panels, which aims to support the integration of existing recycling technologies and collection schemes using a holistic approach for ensuring feasibility and reducing environmental impact. The framework reviews current recycling methodologies for PV waste and the state of PV markets, including PV uptake, waste stream forecast, collection and logistic strategies. Additionally, South Australia is used as the context of analysis for a case study where the framework is applied to identify the potential strategies for handling and collection of end-of-life PV panels based on current PV uptake and waste stream forecast. As a result, capital, transportation and operation costs can be reduced, contributing to lower overall recycling cost for the PV waste treatment and a more efficient reverse logistic system.

Experimental Kinetic Analysis of Potassium Extraction from Ultrapotassic Syenite Using NaCl-CaCl2 Salt Mixture.

This kinetic experimental analysis reports on the application of a eutectic NaCl-CaCl2 salt system for the extraction of potassium from ultrapotassic microsyenite. The reaction parameters, time, temperature, salt composition, and salt to ore ratio, were systematically analyzed. It was found that a salt mixture increases the potassium cation extraction in comparison with using either pure NaCl or pure CaCl2. It was also found that adding CaCl2 into pure NaCl has a considerably stronger effect on increasing the potassium recovery than adding NaCl to pure CaCl2. The salt as a melting agent offers a reduction in the reaction temperature due to its lower melting temperature when compared to pure salts (NaCl or CaCl2). Approximately 70% of K+ in the deposit was extracted at 650 °C. Different characteristic methods have been used to understand the reaction mechanism of the salt mixture and ore, as well as to qualify and quantify the end product mineral phases.

Recent progress and performance evaluation for polyaniline/graphene nanocomposites as supercapacitor electrodes.

Polyaniline (PANi)/graphene nanocomposites have attracted tremendous interest because of their great potential in electrochemical energy storage applications, especially supercapacitors. We herein focus on the composite synthesis, device fabrication and particularly various techniques for the improvement of electrochemical performance. It is imperative to take close control of the interface in these nanostructured composites, which thus would lead to the desired synergistic effects and cyclic stability with the efficient diffusion of electrolyte ions and electrons. Challenges and perspectives are discussed for the development of highly efficient PANi/graphene electrodes for supercapacitors.

'Chocolate' silver nanoparticles: Synthesis, antibacterial activity and cytotoxicity.

HYPOTHESIS: Silver nanoparticles (AgNPs) have emerged as a powerful weapon against antibiotic resistant microorganisms. However, most conventional AgNPs syntheses require the use of hazardous chemicals and generate toxic organic waste. Hence, in recent year's, plant derived and biomolecule based synthetics have has gained much attention. Cacao has been used for years for its medicinal benefits and contains a powerful reducing agent - oxalic acid. We hypothesized that, due to the presence of oxalic acid, cacao extract is capable of reducing silver nitrate (AgNO3) to produce AgNPs. EXPERIMENTS: In this study, AgNPs were synthesized by using natural cacao extract as a reducing and stabilizing agent. The reaction temperature, time and reactant molarity were varied to optimize the synthesis yield. FINDINGS: UV-visible spectroscopy (UV-vis), dynamic light scattering (DLS) and transmission electron microscopy (TEM) characterization demonstrated that the synthesized AgNPs were spherical particles ranging in size from 35 to 42.5nm. The synthesized AgNPs showed significant antibacterial activity against clinically relevant pathogens such as Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Staphylococcus epidermidis. Importantly, these green AgNPs are not cytotoxic to human dermal fibroblasts (HDFs) at concentrations below 32µg/ml. We conclude that cacao-based synthesis is a reproducible and sustainable method for the generation of stable antimicrobial silver nanoparticles with low cytotoxicity to human cells. The AgNPs synthesized in this work have promising properties for applications in the biomedical field.

Influence of immobilized quaternary ammonium group surface density on antimicrobial efficacy and cytotoxicity.

Bacterial colonization of medical devices causes infections and is a significant problem in healthcare. The use of antibacterial coatings is considered as a potential solution to this problem and has attracted a great deal of attention. Using concentration density gradients of immobilized quaternary ammonium compounds it was demonstrated that a specific threshold of surface concentration is required to induce significant bacterial death. It was determined that this threshold was 4.18% NR4(+) bonded nitrogen with a surface potential of + 120.4 mV. Furthermore, it is shown for the first time that adhesion of constituents of the culture medium to the quaternary ammonium modified surface eliminated any cytotoxicity towards eukaryotic cells such as primary human fibroblasts. The implications of this type of surface fouling on the antimicrobial efficacy of surface coatings are also discussed.

Elastomeric composites based on carbon nanomaterials.

Carbon nanomaterials including carbon black (CB), carbon nanotubes (CNTs) and graphene have attracted increasingly more interest in academia due to their fascinating properties. These nanomaterials can significantly improve the mechanical, electrical, thermal, barrier, and flame retardant properties of elastomers. The improvements are dependent on the molecular nature of the matrix, the intrinsic property, geometry and dispersion of the fillers, and the interface between the matrix and the fillers. In this article, we briefly described the fabrication processes of elastomer composites, illuminated the importance of keeping fillers at nanoscale in matrices, and critically reviewed the recent development of the elastomeric composites by incorporating CB, CNTs, and graphene and its derivatives. Attention has been paid to the mechanical properties and electrical and thermal conductivity. Challenges and further research are discussed at the end of the article.

Plasma polymer-functionalized silica particles for heavy metals removal.

Highly negatively charged particles were fabricated via an innovative plasma-assisted approach for the removal of heavy metal ions. Thiophene plasma polymerization was used to deposit sulfur-rich films onto silica particles followed by the introduction of oxidized sulfur functionalities, such as sulfonate and sulfonic acid, via water-plasma treatments. Surface chemistry analyses were conducted by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectroscopy. Electrokinetic measurements quantified the zeta potentials and isoelectric points (IEPs) of modified particles and indicated significant decreases of zeta potentials and IEPs upon plasma modification of particles. Plasma polymerized thiophene-coated particles treated with water plasma for 10 min exhibited an IEP of less than 3.5. The effectiveness of developed surfaces in the adsorption of heavy metal ions was demonstrated through copper (Cu) and zinc (Zn) removal experiments. The removal of metal ions was examined through changing initial pH of solution, removal time, and mass of particles. Increasing the water plasma treatment time to 20 min significantly increased the metal removal efficiency (MRE) of modified particles, whereas further increasing the plasma treatment time reduced the MRE due to the influence of an ablation mechanism. The developed particulate surfaces were capable of removing more than 96.7% of both Cu and Zn ions in 1 h. The combination of plasma polymerization and oxidative plasma treatment is an effective method for the fabrication of new adsorbents for the removal of heavy metals.

Antibacterial Plasma Polymer Films Conjugated with Phospholipid Encapsulated Silver Nanoparticles.

Medical device associated infections are a persistent medical problem which has not found a comprehensive solution yet. Over the last decades, there have been intense research efforts toward developing antibacterial coatings that could potentially improve medical outcomes. Silver nanoparticles have attracted a great deal of attention as a potent alternative to conventional antibiotics. Herein, we present a biologically inspired approach to synthesize phospholipid encapsulated silver nanoparticles and their surface immobilization to a functional plasma polymer interlayer to generate antibacterial coatings. The antibacterial efficacy of the coatings was evaluated against three medically relevant pathogens including the Gram-positive Staphylococcus aureus and Staphylococcus epidermidis, and the Gram-negative Pseudomonas aeruginosa. The innate immune response to the coatings was assessed in vitro using primary bone marrow derived macrophages (BMDM). Any potential cytotoxicity was studied with primary human dermal fibroblasts (HDFs). Overall, the coatings had excellent inhibition of bacterial growth. We also observed reduced expression of pro-inflammatory cytokines from BMDM which suggests a reduced inflammatory response. The combined properties of coatings developed in this study may make them a good candidate for application on medical devices such as catheters and wound dressings.

Synthesis and surface immobilization of antibacterial hybrid silver-poly(l-lactide) nanoparticles.

Infections associated with medical devices are a substantial healthcare problem. Consequently, there has been increasing research and technological efforts directed toward the development of coatings that are capable of preventing bacterial colonization of the device surface. Herein, we report on novel hybrid silver loaded poly(L-lactic acid) nanoparticles (PLLA-AgNPs) with narrowly distributed sizes (17 ± 3 nm) prepared using a combination of solvent evaporation and mini-emulsion technology. These particles were then immobilized onto solid surfaces premodified with a thin layer of allylamine plasma polymer (AApp). The antibacterial efficacy of the PLLA-AgNPs nanoparticles was studied in vitro against both gram-positive (Staphylococcus epidermidis) and gram-negative (Escherichia coli) bacteria. The minimal inhibitory concentration values against Staphylococcus epidermidis and Escherichia coli were 0.610 and 1.156 µg · mL(-1), respectively. The capacity of the prepared coatings to prevent bacterial surface colonization was assessed in the presence of Staphylococcus epidermidis, which is a strong biofilm former that causes substantial problems with medical device associated infections. The level of inhibition of bacterial growth was 98%. The substrate independent nature and the high antibacterial efficacy of coatings presented in this study may offer new alternatives for antibacterial coatings for medical devices.

Substrate independent silver nanoparticle based antibacterial coatings.

Infections arising from bacterial adhesion and colonization on medical device surfaces are a significant healthcare problem. Silver based antibacterial coatings have attracted a great deal of attention as a potential solution. This paper reports on the development of a silver nanoparticles based antibacterial surface that can be applied to any type of material surface. The silver nanoparticles were surface engineered with a monolayer of 2-mercaptosuccinic acid, which facilitates the immobilization of the nanoparticles to the solid surface, and also reduces the rate of oxidation of the nanoparticles, extending the lifetime of the coatings. The coatings had excellent antibacterial efficacy against three clinically significant pathogenic bacteria i.e. Staphylococcus epidermidis, Staphylococcus aureus and Pseudomonas aeruginosa. Studies with primary human fibroblast cells showed that the coatings had no cytotoxicity in vitro. Innate immune studies in cultures of primary macrophages demonstrated that the coatings do not significantly alter the level of expression of pro-inflammatory cytokines or the adhesion and viability of these cells. Collectively, these coatings have an optimal combination of properties that make them attractive for deposition on medical device surfaces such as wound dressings, catheters and implants.

Development of oxidized sulfur polymer films through a combination of plasma polymerization and oxidative plasma treatment.

A novel two-step process consisting of plasma polymerization and oxidative plasma treatment is introduced in this article for the first time for the fabrication of -SO(x)(H)-functionalized surfaces. Plasma-polymerized thiophene (PPT) was initially deposited onto silicon wafers and subsequently SO(x)(H)-functionalized using air or oxygen plasma. The effectiveness of both air and oxygen plasma treatments in introducing sulfur-oxygen groups into the PPT film was investigated as the plasma input specific energy and treatment time were varied. The surface chemistries of untreated and treated PPT coatings were analyzed by X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectroscopy (ToF-SIMS), whereas spectroscopic ellipsometry was used to evaluate the film thickness and ablation rate. Surface chemistry analyses revealed that high concentrations of -SO(x)(H) functionalities were generated on the surface upon either air or oxygen plasma treatment. It was found that, at low plasma input energies, the oxidation process was dominant whereas, at higher energies, ablation of the film became more pronounced. The combination of thiophene plasma polymerization and air/oxygen plasma treatment was found to be a successful approach to the fabrication of -SO(x)(H)-functionalized surfaces.

Synthesis and antibacterial properties of a hybrid of silver-potato starch nanocapsules by miniemulsion/polyaddition polymerization.

Controlled synthesis of hollow polymeric nanocapsules has attracted significant attention in a wide range of applications. This paper reports a facile method for the synthesis of hybrid starch nanocapsules decorated with silver nanoparticles using the inverse miniemulsion polyaddition technique. Silver nanoparticles are formed and embedded in the shell of the nanocapsules during the polyaddition process without using any additional reducing agents. We found that silver also acts as a lipophobe that builds up osmotic pressure in the droplets facilitating the formation of stable round shaped nanocapsules. The nanocapsules' shell thickness could be tuned from 13 to 29 nm by varying the amount of cross-linker. We investigated the minimum inhibitory concentration (MIC) of the nanocapsules against Staphylococcus epidermidis ATCC 35984 and Escherichia coli ATCC 25922 which are two bacteria of medical relevance. The silver nanoparticle decorated nanocapsules showed antibacterial properties against both bacteria at the MIC of 2.315 µg mL-1 while control nanocapsules without silver had no antibacterial activity.

Hydrophobic plasma polymer coated silica particles for petroleum hydrocarbon removal.

In recent years, functionalized hydrophobic materials have attracted considerable interest as oil removal agents. This investigation has applied plasma polymerization as a novel method to develop hydrophobic and oleophilic particles for water purification. 1,7-Octadiene was plasma polymerized onto silica particles using a radio frequency inductively coupled reactor fitted with a rotating chamber. Plasma polymerized 1,7-octadiene (ppOD) films were deposited using plasma power of 40 W and monomer flow rate of 2 sccm, while polymerization time was varied from 5 to 60 min. The surface chemistry of ppOD coated particles was investigated via X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectroscopy, while Washburn capillary rise measurements were applied to evaluate the hydrophobicity and oleophilicity of the particles. The effectiveness of ppOD coated particles for the removal of hydrophobic matter from water was demonstrated by adsorption of motor oil, kerosene, and crude oil. Petroleum hydrocarbon removal was examined by varying removal time and particle mass. The morphology of oil-loaded ppOD coated particles was examined via environmental scanning electron microscopy observations. Increasing the polymerization time increased the concentration of hydrocarbon functionalities on the surface, thus also increasing the hydrophobicity and oil removal efficiency (ORE). The ppOD coated particles have shown to have excellent ORE. These particles were capable of removing 99.0-99.5% of high viscosity motor oil in 10 min, while more than 99.5% of low viscosity crude oil and kerosene was adsorbed in less than 30 s. Plasma polymerization has shown to be a promising approach to produce a new class of materials for a fast, facile, and efficient oil removal.

Influence of film stability and aging of plasma polymerized allylamine coated quartz particles on humic acid removal.

Plasma polymerized allylamine (ppAA) films have been successfully deposited on to the surface of quartz particles via a rotating barrel plasma reactor for humic acid removal. The films were deposited at a power of 25 W, allylamine flow rate of 4.4 sccm and polymerization times of 5 to 60 min. X-ray photoelectron spectroscopy was used to investigate the influence of short-term stirring in water and film age on surface chemistry. Stirring results in a reduction in the nitrogen concentration, which was greatest for shorter polymerization times. Film aging of up to 52 weeks appeared to result in a reduction in the concentration of C-N species. The influence of batch, recycling, and film age on humic acid removal was investigated. Humic acid removal appeared to be reproducible across three separate batches for polymerization times of 20 min or more, which was attributed to film thickness. Recycling of the ppAA films was most successful at pH 11 for up to 4 humic acid removal/regeneration cycles. Successful regeneration at pH 11 was attributed to electrostatic repulsion of the adsorbed humic acid molecules. Decreasing the pH of the regeneration solution reduced the number of successful regeneration cycles due to greater retention of adsorbed humic acid via electrostatic attraction. Film age appears to have minimal effect on humic acid removal where freshly deposited and 52-week-old films removed similar masses of humic acid. Successful production and development of ppAA coated quartz particles has resulted in a functional material that can be incorporated into a water treatment system to improve water quality.

Hydrolytic stability of mesoporous zirconium titanate frameworks containing coordinating organic functionalities.

The hydrolytic stability of lanthanide and actinide selective mono- and polyphosphonate-functionalized mesoporous zirconium titanium oxide adsorbents has been investigated in nitric acid solutions. Hydrolytic degradation of the surfaces, as measured through the fractional loss of phosphorus and elements of the oxide framework, increased by more than an order of magnitude as the nitric acid concentration was increased from 0 to 2 mol/L. The unfunctionalized parent oxide suffered considerable dissolution in 2 mol/L acid over a period of 72 h. Under identical conditions, the fractional Zr and Ti release was reduced to 1 × 10(-2) for monophosphonate functionalized hybrids and reached as low as 1 × 10(-6) for trisphosphonate functionalized variants. The bisphosphonates showed intermediate values. The leaching of P, Zr and Ti was found to be incongruent with the Zr leaching to a lesser extent implying enhanced stability of the Zr-O-P bond. Quantitative analysis of the dissolution kinetics indicated a parabolic dissolution model with a rate constant in the range of 0.5-1.5 mg g(-1) min(-1/2) for the elemental leaching of P, Ti, and Zr. The leaching of Zr from the mesoporous matrix was relatively more complex than for the other elements with evidence of a leaching mechanism involving two processes. ToF-SIMS and DRIFT analysis demonstrated that after leaching in 2 M HNO3 for 24 h, a significant proportion of grafted ligands remained on the surface. The oxide functionalized with amino trismethylenephosphonic acid, which had previously shown excellent (153)Gd(3+) selectivity, was demonstrated to have outstanding stability, with low fractional elemental losses and preservation of mesoporous texture even after leaching for 24 h in 2 M HNO3. This suggests this particular hybrid to be worthy of additional study.

Melt compounding with graphene to develop functional, high-performance elastomers.

Rather than using graphene oxide, which is limited by a high defect concentration and cost due to oxidation and reduction, we adopted cost-effective, 3.56 nm thick graphene platelets (GnPs) of high structural integrity to melt compound with an elastomer-ethylene-propylene-diene monomer rubber (EPDM)-using an industrial facility. An elastomer is an amorphous, chemically crosslinked polymer generally having rather low modulus and fracture strength but high fracture strain in comparison with other materials; and upon removal of loading, it is able to return to its original geometry, immediately and completely. It was found that most GnPs dispersed uniformly in the elastomer matrix, although some did form clusters. A percolation threshold of electrical conductivity at 18 vol% GnPs was observed and the elastomer thermal conductivity increased by 417% at 45 vol% GnPs. The modulus and tensile strength increased by 710% and 404% at 26.7 vol% GnPs, respectively. The modulus improvement agrees well with the Guth and Halpin-Tsai models. The reinforcing effect of GnPs was compared with silicate layers and carbon nanotube. Our simple fabrication would prolong the service life of elastomeric products used in dynamic loading, thus reducing thermosetting waste in the environment.

Gd2O3 nanoparticles: size-dependent nuclear magnetic resonance.

In this communication, we demonstrate that there is an optimum gadolinium oxide (Gd(2)O(3)) nanoparticle size of 2.3 nm; in the presence of Gd(2)O(3) particles smaller and larger than this critical size, the spin-lattice relaxation rate (T(1) = 1/r(1)) of water protons at 7.0 T drastically decreases. Since r(1) is directly related to the quality of magnetic resonance imaging, the results presented here have significant implications for clinical diagnostics.

Plasma polymerized allylamine coated quartz particles for humic acid removal.

Allylamine plasma polymerization has been used to modify the surface of quartz particles for humic acid removal via an inductively coupled rotating barrel plasma reactor. Plasma polymerized allylamine (ppAA) films were deposited at a power of 25 W, allylamine flow rate of 4.4 sccm and polymerization times of 5-60 min. The influence of polymerization time on surface chemistry was investigated via X-ray photoelectron spectroscopy (XPS), time of flight secondary ion mass spectrometry (ToF-SIMS) and electrokinetic analysis. Acid orange 7 adsorption/desorption quantified the number of surface amine groups. Humic acid removal via ppAA quartz particles was examined by varying pH, removal time, humic acid concentration, and particle mass. Increasing the polymerization time increased the concentration of amine groups on the ppAA quartz surface, thus also increasing the isoelectric point. ToF-SIMS demonstrated uniform distribution of amine groups across the particle surface. Greatest humic acid removal was observed at pH 5 due to electrostatic attraction. At higher pH values, for longer polymerization times, humic acid removal was also observed due to hydrogen bonding. Increasing the initial humic acid concentration increased the mass of humic acid removed, with longer polymerization times exhibiting the greatest increases. Plasma polymerization using a rotating plasma reactor has shown to be a successful method for modifying quartz particles for the removal of humic acid. Further development of the plasma polymerization process and investigation of additional contaminants will aid in the development of a low cost water treatment system.

Extraordinary optical transmission: coupling of the Wood-Rayleigh anomaly and the Fabry-Perot resonance.

In this Letter, we demonstrate for the first time that by combining the effects of the Wood-Rayleigh anomaly (WRA) and the Fabry-Perot (FP) resonance, transmission efficiencies of one-dimensional metallo-dielectric gratings on substrates can be significantly improved compared to when these two phenomena work separately. Results of combining the WRA and the FP resonance can be utilized to eliminate the necessity of using the index matching technique and the core-shell structure for enhancing the performance of extraordinary optical transmission devices. Further, the outcomes of combining the WRA and the FP resonance can elucidate some of the unexplained results in the literature.

The application of surface engineered silica for the treatment of sugar containing wastewater.

The removal of sucrose and fructose from water at various high concentrations by surface engineered silica (SES) was studied using dissolved sugar in pure water. The results indicate that sugar at concentrations of up to 800 g/L can be removed by SES at a relatively high dose of 250 to 300 g/L. Based on these results, process water from a soft drink filling station which was contaminated by sugar, flavour components, Escherichia coli, Pseudomonas aeruginosa bacteria and Candida pelliculosa yeast were treated to study the performance of SES using actual process water samples by analysing turbidity, biological oxygen demand (BOD), UV absorption, and various other standard parameters, and microbial tests. The study shows that at a dose of 100 g/L of SES bacterial contamination as well as turbidity, BOD and UV absorption can be significantly reduced. However, the study found the yeast species Candida pelliculosa could not be removed from the water samples.