Synthetic Water-soluble Polymers Research Articles

Identification of Water-Soluble Polymers through Discrimination of Multiple Optical Signals from a Single Peptide Sensor.

The pollution of water environments is a worldwide concern. Not only marine pollution by plastic litter, including microplastics, but also the spillage of water-soluble synthetic polymers in wastewater have recently gained increasing attention due to their potential risks to soil and water environments. However, conventional methods to identify polymers dissolved in water are laborious and time-consuming. Here, we propose a simple approach to identify synthetic polymers dissolved in water using a peptide-based molecular sensor with a fluorophore unit. Supervised machine learning of multiple fluorescence signals from the sensor, which specifically or nonspecifically interacted with the polymers, was applied for polymer classification as a proof of principle demonstration. Aqueous solutions containing different polymers or multiple polymer species with different mixture ratios were identified successfully. We found that fluorophore-introduced biomolecular sensors have great potential to provide discriminative information regarding water-soluble polymers. Our approach based on the discrimination of multiple optical signals of water-soluble polymers from peptide-based molecular sensors through machine learning will be applicable to next-generation sensing systems for polymers in wastewater or natural environments.

Structural and mechanical properties of new sizing compositions based on natural and synthetic water-soluble polymers

In the article results of studying specific structurally-mechanical properties new developed sizing compositions on the basis of сorn starch and water-soluble synthetic polymeric preparations such as K-4 and uniflock made in Company "Navoiazot" are given. It is established that, introduction in starch pastes acrylates leads to increase coefficient of thixotropic restoration, i.e. to increase of speed relaxation processes.

Water-soluble polymers in agriculture: xanthan gum as eco-friendly alternative to synthetics.

SummaryWater‐soluble polymers (WSPs) are a versatile group of chemicals used across industries for different purposes such as thickening, stabilizing, adhesion and gelation. Synthetic polymers have tailored characteristics and are chemically homogeneous, whereas plant‐derived biopolymers vary more widely in their specifications and are chemically heterogeneous. Between both sources, microbial polysaccharides are an advantageous compromise. They combine naturalness with defined material properties, precisely controlled by optimizing strain selection, fermentation operational parameters and downstream processes. The relevance of such bio‐based and biodegradable materials is rising due to increasing environmental awareness of consumers and a tightening regulatory framework, causing both solid and water‐soluble synthetic polymers, also termed ‘microplastics’, to have come under scrutiny. Xanthan gum is the most important microbial polysaccharide in terms of production volume and diversity of applications, and available as different grades with specific properties. In this review, we will focus on the applicability of xanthan gum in agriculture (drift control, encapsulation and soil improvement), considering its potential to replace traditionally used synthetic WSPs. As a spray adjuvant, xanthan gum prevents the formation of driftable fine droplets and shows particular resistance to mechanical shear. Xanthan gum as a component in encapsulated formulations modifies release properties or provides additional protection to encapsulated agents. In geotechnical engineering, soil amended with xanthan gum has proven to increase water retention, reduce water evaporation, percolation and soil erosion – topics of high relevance in the agriculture of the 21st century. Finally, hands‐on formulation tips are provided to facilitate exploiting the full potential of xanthan gum in diverse agricultural applications and thus providing sustainable solutions.

Chemically Room Temperature Crosslinked Polyvinyl Alcohol (PVA) with Anomalous Microwave Absorption Characteristics.

Polyvinyl alcohol (PVA) is a great interest polymer due to its excellent film-forming, emulsifying, microwave dielectrics and adhesive properties. However, PVA is a water-soluble synthetic polymer making it susceptible to environmental factors. In this work, PVA is crosslinked at room temperature using divinyl sulfone (DVS) as a crosslinker, and the obtained crosslinked PVA (XPVA) is water-insoluble. Crosslinking mechanism is proposed, thermal and microwave dielectric properties of X-PVA are studied. The studies revealed that X-PVA has better thermal stability and microwave absorption properties. The obtained minimum reflection loss (RL) of X-PVA is -23 dB (filler-free) with entire X-band (8.2-12.4 GHz) absorption bandwidth (RL ≤ -10 dB), indicating excellent microwave absorption properties. Artificial neural network (ANN) predicted RL of X-PVA also matched well with the experimental data. Electromagnetic power simulation suggests that the microwave power absorption density due to the dielectric loss is intrinsically predominant in X-PVA compared to the pristine PVA. Further, the ratio of electromagnetic energy to heat energy conversion power (absorption) of X-PVA is much higher than pristine PVA, indicating the suitability for self-powered devices. X-PVA also fulfils many commercial requirements such as bulk level facile synthesis, large area fabrications, ultralight, and inexpensive.

Polyvinyl alcohol increased growth, migration, invasion, and sphere size in the PK-8 pancreatic ductal adenocarcinoma cell line

Polyvinyl alcohol (PVA) is a water-soluble synthetic polymer used in eye drops, embolization particles, and artificial cartilage. It has also been shown to cause expansion of functional multipotent self-renewing hematopoietic stem cells under serum-free conditions. In this study, we examined the effects of PVA on human pancreatic ductal adenocarcinoma (PDAC) cell lines using 2-dimensional (2D) and 3D-cultures with serum-free medium. In the 2D-culture, PVA-treatment induced an aggregated colony-like appearance in PDAC cells. It increased the growth of PK-8 cells in a dose-dependent manner as well as significantly increasing migration and invasion abilities. qRT-PCR showed an increase in α2 integrin and a decrease in matrix metalloprotease levels in PVA-treated PK-8 cells. Through qRT-PCR analysis, β1 integrin expression at the mRNA level was found to be decreased; however, it was unaltered at the protein level when assessed using FACS analysis.PVA further induced mesenchymal to epithelial transition-like alterations, including increased E-cadherin and decreased Vimentin and N-cadherin expression. Four cancer stem cell (CSC) markers were higher in PVA-treated PK-8 cells compared to controls. In 3D-culture, PVA-treated PK-8 cells showed a rod-like appearance with larger sphere size and higher growth ability. qRT-PCR showed that CSC markers did not increase and 2 of 4 drug transporters had decreased in PVA-treated PK-8 cells. These findings suggest that PVA increases the growth, migration, invasion, and sphere size of PK-8 cells, but does not increase the proportion of pancreatic CSCs under 3D-culture conditions with serum-free medium.

New insights into guar gum as environmentally friendly polymer for enhanced oil recovery in high-salinity and high-temperature sandstone reservoirs

Chemical enhanced oil recovery (EOR) processes are usually used as additives for hydrocarbon production due to its simplicity and relatively reasonable additional production costs. Polymer flooding uses polymer solutions to increase oil recovery by decreasing the water/oil mobility ratio by increasing the viscosity of the displacing water. The commonly used synthetic water-soluble polymer in EOR application is partially hydrolyzed polyacrylamide (HPAM). However, synthetic polymers in general are not attractive because of high cost, environmental concerns, limitation in high temperature, and high-salinity environment. Guar gum is an environmentally friendly natural water-soluble polymer available in large quantities in many countries and widely used in various applications in the oil and gas industry especially in drilling fluids and hydraulic fracturing operations; however, very limited studies investigated on guar as a polymer for EOR and no any study investigated on its uses in high-temperature and high -salinity reservoirs. The objective of this study is to confirm the use of guar gum as a natural polymer for EOR applications in sandstone reservoirs and investigate its applicability for high-temperature and high-salinity reservoirs. The study experimentally investigated rheological characteristics of a natural polymer obtained from guar gum with consideration of high temperature (up to 210 °F) and high salinity (up to 20% NaCl) and tested the guar solution as EOR polymer. The results of this study show that the guar solution can be used as an environmentally friendly polymer to enhance oil recovery. Based on the results, it can be concluded that guar gum shows shear-thinning behavior and strongly susceptible to microbial degradation but also shows a very good properties stability in high temperature and salinity, where in low shear rate case, about 100 cp viscosity can be achieved at 210 °F for polymer prepared in deionized water. Guar polymer shows good viscosity in the presence of 20% NaCl where the viscosity is acceptable for temperature less than 190 °F. Also, the flooding experiment shows that the recovery factor can be increased by 16%.

Determination of mechanical and hydraulic properties of polyacrylamide-added bentonite-sand mixtures

Bentonite-sand mixtures are typically used in engineering applications such as cutoff walls for waste containment facilities or barriers in landfills and freshwater reservoirs. However, low or reduced mechanical and hydraulic performance of a bentonite-sand mixture might result in the failure of the engineering structure. In order to enhance the mechanical and hydraulic properties of a bentonite-sand mixture, an anionic and a cationic polyacrylamides with a content of 1, 2, 5, 10, and 15% respectively were added to the bentonite-sand mixtures. The polyacrylamides used in this study were water-soluble synthetic polymers with high molecular weights. They had enhanced flocculation capability when coming into contact with soil and water. Standard Proctor compaction, consolidated-drained direct shear, unconfined compression, falling-head permeability, and free swell tests were performed on the bentonite-sand mixtures that had different bentonite contents. Test results indicated that cohesion, unconfined compressive strength, maximum dry unit weight, and swell index increased while internal frictional angle, permeability, and optimum water content decreased as a result of the polyacrylamide addition. The rate of change was much higher when the polyacrylamide content was increased up to 2%. The performance of the anionic polyacrylamide was found to be slightly better than that of the cationic polyacrylamide in terms of both strength and permeability. In conclusion, 2% anionic polyacrylamide addition resulted in a sufficient increase in the shear and compressive strength, a slight increase in the swell index, and a sufficient decrease in the permeability of the bentonite-sand mixtures.

Cationic polymeric template-mediated preparation of silica nanocomposites.

Biosilicification allows the formation of complex and delicate biogenic silica in near-neutral solutions under ambient conditions. Studies have revealed that, during biosilicification, basic amino acid residues and long-chain polyamines of organic substrates interact electrostatically with negatively charged silicate precursors in solution, catalyzing the polycondensation of silicic acid and accelerating the formation of silica. This mechanism has inspired researchers to explore polymers bearing chemical similarity with these organic matrices as cationic templates for biomimetic silicification. Such templates can be classified into two general categories based on the physical forms applied. One is a solution of water-soluble cationic polymers, either natural or synthetic, used as is for silicification. The other category includes various microscopically shaped entities made of cationic polymer-containing molecules, in the form of micelles, vesicles, crystalline aggregates, latex particles, and microgels. Combined with controlled polymerization and other techniques, these preorganized templates can be tailor designed in terms of sizes and morphologies to allow further expansion of properties and functions. In this review, notable research progress for both categories of silicification under biomimetic conditions is discussed. With the merits of silica and cationic polymers seamlessly integrated, the potential of such versatile nanocomposites in biomedical as well as energy and environmental applications is also briefly highlighted.

Cultivation of filamentous fungi for attack on synthetic polymers via biological Fenton chemistry.

Environmental pollution with synthetic polymers (commonly named plastics) nowadays poses serious threats to the environment and human health. Unfortunately, most conventional plastics are highly recalcitrant even under conditions known to be favorable for microbial degradation. Expanding the knowledge regarding opportunities and limitations of the microbial degradability of plastics would largely contribute to the development of adequate decontamination and management strategies for plastic pollution. This chapter provides cultivation approaches to be applied for the characterization of eco-physiologically diverse asco- and basidiomycete fungi with respect to their ability to attack solid and water-soluble synthetic polymers with the help of quinone redox cycling-based Fenton-type reactions, which result in the production of highly reactive hydroxyl radicals. These reactive oxygen species are the strongest oxidants known from biological systems. However, their potential employment by fungi dwelling in diverse habitats as a biodegradation tool to attack synthetic polymers is still insufficiently explored.

Morphology control and ionic crosslinking of pectin domains to enhance the toughness of solvent cast PVA/pectin blends

AbstractBlending water soluble synthetic polymers, such as polyvinyl alcohol (PVA), with natural polymers, such as pectin, has many advantages. However, due to the brittle nature of pectin, the mechanical properties become inferior in the blends. In this work, two strategies to enhance the toughness and tensile strength of solvent cast PVA/pectin blends are presented. This study shows that the tensile strength and toughness of PVA/pectin 80/20 blends can be enhanced by decreasing the solvent evaporation rate. The phase separation proceeds through 'nucleation and growth' and spinodal decomposition, respectively, at lower and higher rates of solvent evaporation. The equilibrium phase morphology has spherical domains of pectin dispersed in the PVA matrix. The size of the pectin domains and the separation between them are controlled by the solvent evaporation rate. At higher rates of solvent evaporation, pectin domains are larger and farther apart from each other and vice versa. Ionically crosslinking the pectin domains with calcium, further enhances the tensile strength and toughness of the blends compared to that of pure PVA. When the pectin domains are small, the failure happens at larger strains through 'cavitation' and 'shear yielding' and when pectin domains are large, the failure happens at smaller strains and the failure mechanism shifts to 'multiple crazing'.

Interaction of Ionenes with Lipid Membrane: Unusual Impact of Charge Density.

Synthetic water-soluble polymers are increasingly used for gene delivery, stabilization, and delivery of proteins, and as prospective antimicrobial and antiviral agents. Therefore, study of their interaction with lipid membranes is of special importance. Herein, we studied interaction of aliphatic cationic ionenes (recently tested for gene delivery efficiency) differed in the length of spacer between charged groups (and therefore in charge density) with anionic lipid membrane. A range of approaches such as measurement of particle size and electrophoretic mobility, liposome integrity, ATR-FTIR spectroscopy, isothermal titration calorimetry as well as atomistic molecular modeling was used. Ionene with a spacer of 10 methylene groups has been shown to be incorporated into membrane and interact with its inner hydrophobic part in contrast to ionenes with shorter spacer, which interacted only with outer polar head groups of lipids staying at the water-membrane interface. It affects membrane integrity and results in a different behavior of the polymer-liposome complexes. These findings are relevant for potential biomedical application of ionenes, including creation of composite polymer-liposome systems for drug delivery.

Synthesis and Stabilization of Gold Nanoparticles Using Water-Soluble Synthetic and Natural Polymers.

Gold nanoparticles (AuNPs) were synthesized and stabilized using the one-pot method and growth seeding, through utilization of synthetic polymers, including poly(N-vinylpyrrolidone) (PVP), poly(ethylene glycol) (PEG), and poly(vinylcaprolactame) (PVCL), as well as natural polysaccharides, including gellan, welan, pectin, and κ-carrageenan. The absorption spectra, average hydrodynamic size, ζ-potential, and morphology of the gold nanoparticles were evaluated based on various factors, such as polymer concentration, molecular mass of polymers, temperature, and storage time. The optimal polymer concentration for stabilization of AuNPs was found to be 4.0 wt % for PVP, 0.5 wt % for gellan, and 0.2 wt % for pectin, welan, and κ-carrageenan. The values of the ζ-potential of polymer-stabilized AuNPs show that their surfaces are negatively charged. Most of the AuNPs are polydisperse particles, though very monodisperse AuNPs were detected in the presence of a 0.5 wt % gellan solution. At a constant polymer concentration of PVP (4 wt %), the average size of the PVP–AuNPs decreased with the decrease of molecular weight, and in the following order: PVP 350 kDa (~25 nm) > PVP 40 kDa (~8 nm) > PVP 10 kDa (~4 nm). The combination of Fourier-transform infrared spectroscopy (FTIR) and Raman spectroscopy revealed that the functional groups of polymers that are responsible for stabilization of AuNPs are lactam ring in PVP, carboxylic groups in gellan and welan, esterified carboxylic groups in pectin, and SO2 groups in κ-carrageenan. Viscometric and proton nuclear magnetic resonance (1H NMR) spectroscopic measurements showed that the temperature-dependent change in the size of AuNPs, and the gradual increase of the intensity of AuNPs at 550 nm in the presence of gellan, is due to the rigid and disordered conformation of gellan that affects the stabilization of AuNPs. The AuNPs synthesized in the presence of water-soluble polymers were stable over a period of 36 days. Preliminary results on the synthesis and characterization of gold nanorods stabilized by polymers are also presented.

Biodegradation of Polyvinyl Alcohol by Thai Indigenous Mixed Microbial Culture

PVA is biodegradable plastic and a water-soluble synthetic polymer that plays a significant role in industry. A large amount of PVA in wastewater causes heavy environmental pollution in terms of accumulation, disposal, and long-term degradation; therefore it must be removed from wastewater before the water is discharged. In this study, NS3 mixed microbial culture, capable of completely degrading 5 g.L-1 polyvinyl alcohol (PVA), was isolated from landfill soil using the enrichment culture method. It completely degraded PVA at an initial concentration in the range 1 - 5 g.L-1 over 5 - 20 days of incubation with continuous shaking at 30 °C. Moreover, mixed microbial cultures were found to remove PVA at a high range concentration of 10 - 25 g.L-1. Urea and glucose added to the medium inhibited PVA degradation by increasing the pH to a strongly alkaline level, which would cause cell viability and enzyme stability. The FT-IR spectra and SEM imaging revealed the mechanisms and the physical degradation of PVA films, respectively. PVA uptake in bacterial cells produced a dent in the cell surface, which represented the consumption of PVA by bacterial cell. The PVA-degrading mixed microbial culture is the first reported in Thailand and can be beneficial in PVA wastewater treatment.

Novel smart composite materials for industrial wastewater treatment and reuse

With the current levels of industrial development it is very difficult to prevent organic pollutants and toxic heavy metals from contaminating water. Thus purification of contaminated industrial water and its reuse is a global concern. The present study highlights application of a novel standalone technology in the form of polymers that efficiently extract a range of organic and inorganic impurities simultaneously for reuse of industrial effluent. Previous studies have focused on water soluble synthetic polymers for removal of organic contaminants, while biodegradable polymers are being used for extraction of toxic metals from water. Our earlier reports already describe a combination of synthetic and natural polymers with the ability to eliminate organic and inorganic spiked impurities from water on a lab scale. In the present work a series of novel smart composite materials have been synthesized and fully characterized. The avant-garde novelty of these materials for simultaneous removal of organic impurities such as phenols, anhydrides, textile dyes, pesticides, herbicides, antibiotics and inorganic heavy metals has been demonstrated and the novel polymers have shown a removal efficiency of more than 90% for each of the contaminants. Furthermore, the established 4-cycle reusability and an extensive reduction in levels of chemical oxygen demand suggests these materials would act as an improvement to the current methods for treating effluent water. The high reproducibility in synthesis, properties and elimination spectrum brands them as promising materials for industrial water remediation and reuse.

Facile and Novel Eco-Friendly Poly(Vinyl Alcohol) Nanofilters Using the Photocatalytic Property of Titanium Dioxide.

This study aimed to develop a highly efficient nanofilter for capturing fine particles using electrostatic forces. Poly(vinyl alcohol) (PVA), a water-soluble synthetic polymer, was selected as the main component of the filter because it can be easily fabricated by electrospinning. Titanium dioxide (TiO2) nanopowder with an anatase structure was applied to the nanofilters as it has the highest photocatalytic activity among the existing photocatalysts. PVA nanofilters fabricated by electrospinning could still be dissolved in water by hydrolysis. Therefore, heat treatment was performed to make the nanofilters stable, thereby forming C=O bonds by keto–enol tautomerization. Structural changes in the PVA nanofilter before and after heat treatment were investigated by X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) analysis. As the TiO2 concentration increased, the fiber diameter of the PVA nanofilter decreased and a homogeneous fiber was obtained. The filtration efficiency and pressure drop also improved significantly, compared to those of the PVA-only nanofilter. Moreover, we observed eco-friendly decomposition of the PVA/TiO2 nanofilter into water and carbon dioxide by a photocatalytic reaction under UV irradiation.

Iron-Catalysed Radical Polymerisation by Living Bacteria.

The ability to harness cellular redox processes for abiotic synthesis might allow the preparation of engineered hybrid living systems. Towards this goal we describe a new bacteria-mediated iron-catalysed reversible deactivation radical polymerisation (RDRP), with a range of metal-chelating agents and monomers that can be used under ambient conditions with a bacterial redox initiation step to generate polymers. Cupriavidus metallidurans, Escherichia coli, and Clostridium sporogenes species were chosen for their redox enzyme systems and evaluated for their ability to induce polymer formation. Parameters including cell and catalyst concentration, initiator species, and monomer type were investigated. Water-soluble synthetic polymers were produced in the presence of the bacteria with full preservation of cell viability. This method provides a means by which bacterial redox systems can be exploited to generate "unnatural" polymers in the presence of "host" cells, thus setting up the possibility of making natural-synthetic hybrid structures and conjugates.

Structural analysis of cross-linked poly(vinyl alcohol) using high-field DNP-NMR.

Poly(vinyl alcohol) (PVOH) is a water-soluble synthetic polymer, widely used in materials for functional films and moldings, fiber fabric sizing agents, paper coating resins, and adhesives. PVOH is mainly applied in the form of an aqueous solution, yet after its application, insolubility (water resistance) is required. To achieve this, additives are introduced. These additives used with PVOH are cross-linking agents which react with the hydroxyl groups and modified functional groups in PVOH. Because of the poor reactivity of unmodified PVOH, it does not react with cross-linking agents that have functional reactive groups. Therefore, modified PVOH that reacts with a cross-linking agent more successfully is required. These chemical bonding sites are so low in abundance that it is difficult to characterize the cross-linking structure. Solid-state 13C NMR is a powerful technique that can be used for the structural analysis of a polymer material. However, its sensitivity is low, hence it is difficult to determine crosslinking in a polymer, as it makes up only a small proportion of the product. Therefore, solid-state 13C NMR sensitivity can be enhanced by high-field dynamic nuclear polarization (DNP) using strong electron polarization. In this study, the reaction of acetoacetylated PVOH with a cross-linking agent, adipic dihydrazide, was analyzed. This crosslinked PVOH is the most popular vinyl alcohol polymer on the commercial market. The sensitivity enhanced 13C NMR spectra reveal that the carbonyl of the acetoacetyl group of PVOH crosslinks with adipic hydrazide by forming an imine bond (>C Created by potrace 1.16, written by Peter Selinger 2001-2019 ]]> N–) this study also shows that the product has only seven crosslinking sites per molecular chain with a polymerization degree of 1000 and is water resistant.

Influence of Sodium Salts on the Swelling and Rheology of Hydrophobically Cross-linked Hydrogels Determined by QCM-D.

Hydrophobically modified copolymers provide a versatile platform of hydrogel materials for diverse applications, but the influence of salts on the swelling and material properties of this class of hydrogels has not been extensively studied. Here, we investigate model hydrogels with three different sodium salts with anions chosen from the classic Hofmeister series to determine how these counterions influence the swelling and mechanical properties of neutral hydrogels. The gel chosen was based on a statistical copolymer of dimethylacrylamide and 2-(N-ethylperfluorooctane sulfonamido) ethyl acrylate (FOSA). Our measurements utilize a quartz crystal microbalance with dissipation (QCM-D) to quantify both swelling and rheological properties of these gels. We find that a 1 mol/L solution of Na2SO4, corresponding to a kosmotropic anion, leads to nearly a 2.6-fold gel deswelling and correspondingly, the complex modulus increases by an order of magnitude under these solution conditions. In contrast, an initial increase in swelling and then a swelling maximum is observed for a 0.02 mol/L concentration in the case of a chaotropic anion, NaClO4, but the changes in the degree of gel swelling in this system are not directly correlated with changes in the gel shear modulus. The addition of NaBr, an anion salt closer to the middle of the chaotropic to kosmotropic range, leads to hydrogel deswelling where the degree of deswelling and the shear modulus are both nearly independent of salt concentration. Overall, the observed trends are broadly consistent with more kosmotropic ions causing diminished solubility ("salting out") and strongly chaotropic ions causing improved solubility ("salting in"), a trend characteristic of the Hoffmeister series governing the solubility of many proteins and synthetic water-soluble polymers, but trends in the shear stiffness with gel swelling are clearly different from those normally observed in chemically cross-linked gels and are correspondingly difficult to interpret. The salt specificity of swelling and mechanical properties of nonionic hydrogels is important for any potential application in which a wide range of salt concentrations and types are encountered.

Biocompatible microlasers based on polyvinyl alcohol microspheres

Biocompatible microlasers, generally made of bio-derived materials, are promising for biosensing and cell-tracking. These kinds of lasers offer favourable opportunities like biocompatibility and biodegradability but the materials used often require complicated synthesis and high cost. In this work, we demonstrate that polyvinyl alcohol (PVA), a synthetic water-soluble low-cost polymer, with fascinating properties such as good transparency, biocompatibility, biodegradability is an excellent candidate for making laser cavity. Using a simple and effective technique, dye-doped PVA microspheres can be fabricated with various sizes from 10 to 200 μm. These microspheres can act as excellent lasers under optical excitation with a lasing threshold of ∼2 μJ/mm2 and Q factor of lasing modes of ∼3000. The lasing mechanism is studied and it is ascribed to whispering gallery mode (WGM). Size-dependent lasing characteristics including lasing spectrum, quality (Q) factor and lasing threshold are investigated. Owing to the ease of fabrication, the cost-effectiveness, the biocompatibility of the PVA material, our biocompatible microlasers are promising for future biosensing applications.

A Promising Water-Soluble Synthetic Polymer of High Efficiency and Low Cost as Inhibitor for Inhibition of Metals Corrosion: Inhibition of Magnesium Corrosion by Poly (Ethylene Glycol) in Acidic Media

Corrosion inhibition of magnesium (Mg) in hydrochloric acid by poly (ethylene glycol) (PEG) as a water-soluble synthetic polymer has been investigated by both gasometric and weight-loss techniques. A comparable value has been observed from the results obtained from those both two techniques. The inhibition efficiency was found to increase with increasing the inhibitor concentration. The kinetic data were found to fit both Langmuir and Freundlich relationships, but the inhibition action was exhibited in the Freundlich isotherm model. Factors affecting the corrosion rates such as the concentration and geometrical structure of inhibitor, concentration of the corrosive medium, and temperature were examined. The inhibition effect of the PEG on the magnesium metal surface was confirmed by Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), and X-ray diffraction (XRD) techniques. The kinetic parameters were evaluated and a suitable corrosion mechanism consistent with the kinetic results is discussed.