Anionic Polyelectrolyte Research Articles

Delivery system for dexamethasone phosphate based on a Zn2+-crosslinked polyelectrolyte complex of diethylaminoethyl chitosan and chondroitin sulfate

Hybrid nano- and microparticles based on metal ion crosslinked biopolymers are promising carriers for the development of drug delivery systems with improved biopharmaceutical properties. In this work, dexamethasone phosphate-containing particles based on chondroitin sulfate and chitosan or diethylaminoethyl chitosan additionally crosslinked with Zn2+ were prepared. Depending on the polycation/polyanion ratio in the system, anionic and cationic polyelectrolyte complexes (PECs) were obtained. The anionic Zn2+-containing and Zn2+-free PECs had sizes of 154 and 180 nm and ζ-potentials of −22.4 and −27.5 mV, respectively. The cationic Zn2+-containing and Zn2+-free PECs had sizes of 242 and 362 nm and ζ-potentials of 22.4 and 24.7 mV, respectively. The presence of Zn2+ in the system significantly prolonged the release of dexamethasone phosphate from the hybrid polyelectrolyte particle. The resulting release profiles of dexamethasone phosphate were in agreement with the Peppas-Sahlin kinetic model, which considers the combined effects of Fickian diffusion and polymer chain relaxation on the drug release rate. It was shown that the prolongation of drug release was mainly due to swelling and relaxation of the Zn2+ crosslinked polymers. The developed particles exhibited good mucoadhesive properties and pronounced anti-inflammatory activity, making them attractive candidates for biomedical applications.

Effect of shear rate, temperature, and salts on the viscosity and viscoelasticity of semi‐dilute and entangled xanthan gum

AbstractXanthan gum, a naturally‐occurring, high‐molecular‐weight, anionic polyelectrolyte, exhibits significant drag‐reducing properties at low concentrations in water, suggesting promising applications in geothermal networks. The flow behavior of xanthan solutions are explored, specifically at concentrations in the semi‐dilute (1000 ppm by mass) and entangled (4000 ppm) regimes as well as in both water and various salt solutions across a temperature range of 5–85°C. The viscosity and viscoelastic properties of xanthan solutions examine relationships between polyelectrolyte concentration, temperature, and salt concentration. Viscosity decreases by two orders of magnitude in 4000 ppm xanthan solutions in deionized water and with 50 mM NaCl (in the high salt limit) as the temperature increases from 5 to 85°C. Next, the addition of salts affects viscosity differently in the two concentration regimes. Specifically, at 25°C, the zero‐shear rate viscosity upon salt addition decreases by 63% for 1000 ppm solutions (from 0.54 to 0.2 Pa s) but increases by 280% for 4000 ppm solutions (from 28 to 107 Pa s). At 1000 ppm, salt ions cause chain collapse, reducing viscosity; At 4000 ppm, entanglements led to structural changes, resulting in higher viscosity. Furthermore, three salts commonly found in geothermal waters, namely NaCl, Na2CO3, and NaHCO3, exhibited similar changes in viscosity and shear thinning behavior in the entangled regime across temperatures from 5 to 85°C.

Using Artificial Neural Networks to Predict Operational Parameters of a Drinking Water Treatment Plant (DWTP)

The scope of the present study is the estimation of key operational parameters of a drinking water treatment plant (DWTP), particularly the dosages of treatment chemicals, using artificial neural networks (ANNs) based on measurable in situ data. The case study consists of the Aposelemis DWTP, where the plant operator had an estimation of the ANN output parameters for the required dosages of water treatment chemicals based on observed water quality and other operational parameters at the time. The estimated DWTP main operational parameters included residual ozone (O3) and dosages of the chemicals used: anionic polyelectrolyte (ANPE), poly-aluminum chloride hydroxide sulfate (PACl), and chlorine gas (Cl2(g)). Daily measurable results of water sample analysis and recordings from the DWTP Supervisory Control and Data Acquisition System (SCADA), covering a period of 38 months, were used as input parameters for the artificial neural network (1188 values for each of the 14 measurable parameters). These input parameters included: raw water supply (Q), raw water turbidity (T1), treated water turbidity (T2), treated water residual free chlorine (Cl2), treated water concentration of residual aluminum (Al), filtration bed inlet water turbidity (T3), daily difference in water height in reservoir (∆H), raw water pH (pH1), treated water pH (pH2), and daily consumption of DWTP electricity (El). Output/target parameters were: residual O3 after ozonation (O3), anionic polyelectrolyte (ANPE), poly-aluminum chloride hydroxide sulfate (PACl), and chlorine gas supply (Cl2(g)). A total of 304 different ANN models were tested, based on the best test performance (tperf) indicator. The one with the optimum performance indicator was selected. The scenario finally chosen was the one with 100 neural networks, 100 nodes, 42 hidden nodes, 10 inputs, and 4 outputs. This ANN model achieved excellent simulation results based on the best testing performance indicator, which suggests that ANNs are potentially useful tools for the prediction of a DWTP’s main operational parameters. Further research could explore the prediction of water chemicals used in a DWTP by using ANNs with a smaller number of operational parameters to ensure greater flexibility, without prohibitively reducing the reliability of the prediction model. This could prove useful in cases with a much higher sample size, given the data-demanding nature of ANNs.

Fine-tuning the cytotoxicity profile of N,N,N-trimethyl chitosan through trimethylation, molecular weight, and polyelectrolyte complex nanoparticles.

N,N,N-trimethyl chitosan (TMC) is a promising biopolymer for pharmaceutical applications due to its enhanced solubility and bioadhesive properties, though its cytotoxic limitations necessitate careful modification to ensure safety and efficacy. This study sought to investigate whether nanoparticle (NP) formation could reduce the anticipated cytotoxic effects of TMC, thus improving its applicability across a wider spectrum of pharmaceutical uses. TMC's capability to form NPs with anionic polyelectrolytes led to the application of chondroitin sulfate (ChS) in this study. Five TMC samples, varying in degree of trimethylation (DTM 23, 32, 46, 50 and 99%) and molecular weight (Mw, 66-290kDa) were synthesized, and their biocompatibility with human umbilical vein endothelial cells (HUVECs) was assessed. The results revealed a discernible impact of both DTM and Mw on cell viability, with higher DTM and lower Mw correlating with increased toxicity. Cytotoxicity studies against ovarian cancer cell lines SKOV-3 and OVISE showed a clear indication of a higher cytotoxic effect of TMC samples against cancer cells compared to healthy cells (HUVEC). The cytotoxicity against cancer cells also indicated an optimal DTM for maximum efficacy, deviating from a linear trend. The effects of Mw were cell-dependent, introducing complexity to the observed relationship. Additionally, TMC-ChS NPs were successfully prepared, demonstrating a substantial reduction in cytotoxicity compared to TMC alone in all tested cells. This promising outcome suggests the potential of NP formation to fine-tune the cytotoxicity profile of TMC, paving the way for the development of safer and more effective pharmaceutical formulations.

The Effect of Different Surfactants and Polyelectrolytes on Nano-Vesiculation of Artificial and Cellular Membranes.

Nano- and micro-sized vesicular and colloidal structures mediate cell-cell communication. They are important players in the physiology of plants, animals, and humans, and are a subject of increasing interest. We investigated the effect of three surfactants, N-cetylpyridinium chloride (CPC), sodium dodecyl sulfate (SDS), and Triton X-100 (TX100), and two anionic polyelectrolytes, sodium polystyrene sulfonate (NaPSS) and sodium polymethacrylate (NaPMA), on nanoliposomes. In addition, the effect of SDS and TX100 on selected biological membranes (erythrocytes and microalgae) was investigated. The liposomes were produced by extrusion and evaluated by microcalorimetry and light scattering, based on the total intensity of the scattered light (Itot), hydrodynamic radius (Rh), radius of gyration (Rg), shape parameter p (=Rh/Rg,0), and polydispersity index. The EPs shed from erythrocytes and microalgae Dunaliella tertiolecta and Phaeodactylum tricornutum were visualized by scanning electron microscopy (SEM) and analyzed by flow cytometry (FCM). The Rh and Itot values in POPC liposome suspensions with added CPC, SDS, and TX100 were roughly constant up to the respective critical micelle concentrations (CMCs) of the surfactants. At higher compound concentrations, Itot dropped towards zero, whereas Rh increased to values higher than in pure POPC suspensions (Rh ≈ 60-70 nm), indicating the disintegration of liposomes and formation of larger particles, i.e., various POPC-S aggregates. Nanoliposomes were stable upon the addition of NaPSS and NaPMA, as indicated by the constant Rh and Itot values. The interaction of CPC, SDS, or TX100 with liposomes was exothermic, while there were no measurable heat effects with NaPSS or NaPMA. The SDS and TX100 increased the number density of EPs several-fold in erythrocyte suspensions and up to 30-fold in the conditioned media of Dunaliella tertiolecta at the expense of the number density of cells, which decreased to less than 5% in erythrocytes and several-fold in Dunaliella tertiolecta. The SDS and TX100 did not affect the number density of the microalgae Phaeodactylum tricornutum, while the number density of EPs was lower in the conditioned media than in the control, but increased several-fold in a concentration-dependent manner. Our results indicate that amphiphilic molecules need to be organized in nanosized particles to match the local curvature of the membrane for facilitated uptake. To pursue this hypothesis, other surfactants and biological membranes should be studied in the future for more general conclusions.

Preparation of sodium alginate grafted polyelectrolyte by adiabatic polymerization and study on its solution properties

In order to improve the salt resistance and shear resistance of partially hydrolyzed polyacrylamide-based oil displacement agents (they are all anionic polyelectrolytes), this paper proposes the preparation of branched low hydrophobic monomer content sodium alginate grafted hydrophobically modified partially hydrolyzed polyacrylamide P(AM-SA-MO8) using acrylamide (AM), sodium alginate (SA), and non-ionic hydrophobic monomer (MO8) as main raw materials through the method of adiabatic polymerization followed by hydrolysis. The polymerization conditions of P(AM-SA-MO8) were optimized, and the solution properties and oil displacement performance of P(AM-SA-MO8) and P(AM-MO8) (copolymer of AM and MO8) were compared. It was found that the viscosity, resistance to Ca2+/Mg2+, shear resistance, resistance factor (RF), residual resistance factor (RRF), and enhanced oil recovery performance of P(AM-SA-MO8) solution were better than those of P(AM-MO8). Especially in seawater, at 75 ℃, the viscosity of 1500 mg/L P(AM-SA-MO8) solution was 6.5 mpa.s, RF was 6.08, RRF was 2.28, and the enhanced oil recovery was 26.28 % with a injection rate of 4.9 ft/day.

Nanolignin-Facilitated Robust Hydrogels.

Recently, certain challenges and accompanying drawbacks have emerged in the preparation of high-strength and tough polymer hydrogels. Insights from wood science highlight the role of the intertwined molecular structure of lignin and crystalline cellulose in contributing to wood's strength. Herein, we immersed prestretched poly(vinyl alcohol) (PVA) polymer hydrogels into a solution of nanosized lignosulfonate sodium (LS), a water-soluble anionic polyelectrolyte, to creatively reconstruct this similar structure at the molecular scale in hydrogels. The nanosized LS effectively fixed and bundled the prestretched PVA polymers while inducing the formation of dense crystalline domains within the polymer matrix. Consequently, the interwoven structure of crystalline PVA and LS conferred good strength to the composite hydrogels, exhibiting a tensile strength of up to ∼23 MPa, a fracture strain of ∼350%, Young's modulus of ∼17 MPa, toughness of ∼47 MJ/m3, and fracture energy of ∼42 kJ/m2. This hydrogel far outperformed previous hydrogels composed directly of lignin and PVA (tensile strength <1.5 MPa). Additionally, the composite hydrogels demonstrated excellent antifreezing properties (<-80 °C). Notably, the LS-assisted reconstruction technology offers opportunities for the secondary fixation of PVA hydrogel shapes and high-strength welding of hydrogel components. This work introduces an approach for the high-value utilization of LS, a green byproduct of pulp production. LS's profound biomimetic strategy will be applied in multifunctional hydrogel fields.

Preparation of photothermal alginate/chitosan derivative/CuS@polydopamine composite fibers and application in desalination

A polyelectrolyte system consisting of sodium alginate (SA) and quaternary ammonium chitosan (QAC) blended with polydopamine-coated copper sulfide particles (CuS@PDA) was chosen to investigate the function of CuS@PDA in the uniform binary blending of anionic and cationic polyelectrolytes in detail. A smart composite fiber SA/QAC/CuS@PDA was prepared via a dry-wet spinning technique. With the addition of CuS@PDA (about 4.3 % in fiber), the as-prepared SA/QAC/CuS@PDA-0.50 fibers (SQCuS@P-0.50 SCFs) showed notably enhanced intensity 359.2 MPa, excellent moisture response, and photothermal conversion performance, with the temperature increasing from 25.9 to 80.7 °C as irradiated under a 980 nm infrared lamp at distance 20 cm away for 120 s. The photothermal performance was maintained after 6 lighting on-and-off cycles. The tensile strength decreased ~23.8 % after 4 cycles, then remained fixed. The diameter increases to ~480 % in wet state but decreases to the original size in dry state for 10 cycles. When the fabric with 90 wt% SQCuS@P-0.50 SCFs was used as a water evaporator, the water evaporation rate and efficiency were 1.68 kg·m−2·h−1 and 102 % under 1 sun irradiation. This work provides a simple and ecofriendly strategy for fabricating photothermal fabrics by designing and preparing composite fibers.

Polyelectrolyte-coated liposomes microfluidically assembled in one-step for enhancing cell endocytosis and in-vivo immune responses

To enhance the cellular uptake of liposomes, we prepared conventional liposomes with targeting molecules and surface-charged liposomes and evaluated their potential as nano-carriers and vaccine adjuvants by comparing their endocytosis efficiencies using immune cells. Surface-charged liposomes were synthesized via a one-step microfluidic method, which provided a novel, simple, fast, and highly reproducible method for preparing liposomes. Flow cytometry revealed that cationic polyelectrolyte-coated liposomes exhibited higher endocytosis efficiencies (of up to a factor of 100) in A774A.1 cells and JAWs II cells compared with uncoated liposomes or those coated with anionic polyelectrolytes. Positively charged liposomes exhibited some cytotoxicity at quaternary-chitosan coating concentrations higher than 6 mg/mL; however, significantly lower cytotoxicities (by a factor of almost ten) were obtained by protein mixing. Furthermore, BALB/c mice vaccinated with a mixture of Anthrax vaccine adsorbed (AVA) and quaternary chitosan-coated liposomes showed faster and stronger anti-PA IgG inductions compared to those vaccinated with AVA alone, with titers positively correlating with the amount of cationic liposome used. This finding clearly reveals that quaternary chitosan-coated liposomes act as both nano-carriers and vaccine adjuvants that significantly enhance in-vivo immune responses to vaccines with low immunogenicities.

Low Fouling Polyelectrolyte Layer-by-Layer Self-Assembled Membrane for High Performance Dye/Salt Fractionation: Sequence Effect of Self-Assembly.

Layer-by-layer (LbL) self-assembly of oppositely charged polyelectrolytes (PEs) is usually performed on a conventional ultrafiltration base substrate (negative zeta potential) by depositing a cationic PE as a first layer. Herein, we report the facile and fast formation of high performance molecular selective membrane by the nonelectrostatic adsorption of anionic PE on the polyvinylidene fluoride (PVDF, zeta potential -17 mV) substrate followed by the electrostatic LbL assembly. Loose nanofiltration membranes have been prepared via both concentration-polarization (CP-LbL, under applied pressure) driven and conventional (C-LbL, dipping) LbL self-assembly. When the first layer is poly(styrene sodium) sulfonic acid, the LbL assembled membrane contains free -SO3- groups and exhibits higher rejection of Na2SO4 and lower rejection of MgCl2. The reversal of salt rejection occurs when the first layer is quaternized polyvinyl imidazole (PVIm-Me). The membrane (five layers) prepared by first depositing PStSO3Na shows higher rejection of several dyes (97.9 to >99.9%), higher NaCl to dye separation factor (52-1800), and higher dye antifouling performance as compared to the membrane prepared by first depositing PVIm-Me (97.5-99.5% dye rejection, separation factor ∼40-200). However, the C-LbL membrane requires a longer time of self-assembly or higher PE concentration to reach a performance close to the CP-LbL membranes. The membranes exhibit excellent pressure, pH (3-12), and salt (60 g L-1) stability. This work provides an insight for the construction of low fouling and high-performance membranes for the fractionation of dye and salt based on the LbL self-assembly sequence.

Ion-Exchange Polymer Network Enhanced Interfacial Compatibility for Stable and Efficient Inverted Perovskite Solar Cells.

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as a low-cost and water-processable hole transport material has been widely used in various optoelectronic devices. Although the incorporation of anionic polyelectrolyte PSS in PEDOT contributes to superior water solubility, the trade-off between efficiency and stability remains a challenging issue, limiting its reliable application in perovskite solar cells (PSCs). Herein, we proposed an ion-exchange (IE) strategy to effectively control the doping degree, interfacial charge dynamics, and reliability of PEDOT:PSS in PSCs. This IE approach based on hard cation-soft anion rules enabled effective anion exchange between PEDOT:PSS and lithium bis(trifluoromethylsulfonyl)imide (LiTFSI), which favored enhancing the film conductivity, regulating the perovskite crystallization, and reducing the carrier losses at the interfaces. Consequently, a notable increase of the open-circuit voltage from 0.88 to 1.02 V was realized, resulting in a champion efficiency of 18.7% compared to the control (15.4%) in inverted PSCs. More encouragingly, this IE strategy significantly promoted the thermal and environmental stability of unsealed devices by maintaining over 80% of initial efficiencies after 2000 h. This work provides an effective way to regulate the doping state of the PEDOT-based hole transport material and guides the development of robust polymeric conducting materials for efficient perovskite photovoltaics.

Enhancing dispersion stability and recyclability of ceria slurry with polyacrylic acid for improved glass polishing performance

This study aimed to enhance both the dispersion stability and recyclability of micron-sized ceria slurry in glass polishing by incorporating polyacrylic acid (PAA). PAA with a molecular weight of 240 k was very effective as a dispersant for ceria slurry due to its unique surface adsorption and its characteristics as an anionic polyelectrolyte. Using a 240 k-PAA concentration of 1.0 wt% led to significant improvements in polishing performances, as demonstrated by consistent glass removal rates across recycling cycles. Additionally, the study investigated the physico-chemical properties of polishing slurries, such as specific gravity, particle size, zeta potential, and pH. These properties were effectively maintained with the use of PAA as the dispersant, particularly when KOH was used as a pH adjuster. A 100 µm bag-type filtration system was also introduced for handling the micron-sized ceria slurry, highlighting its practical benefits in slurry management. In conclusion, employing 240 k-PAA as a dispersant in micron-sized ceria slurries for Gorilla glass polishing not only maintains quality and stability across recycling cycles but also provides notable economic advantages by enabling the recycling of the slurry.

Effect of Particle-Substrate Interactions on Colloidal Layer Structure Prepared by Convective Self-Assembly Using Polyelectrolyte-Grafted Silica Particles.

Cationic and anionic polyelectrolytes, poly(vinylbenzyl trimethylammonium chloride) (PVBTA) and poly(sodium styrene sulfate) (PSSS), were grafted on the surface of the silica particles, respectively, and then these two types of polyelectrolyte-grafted silica particles were applied to the colloidal layer preparation by convective self-assembly (CSA) using hydrophilic or hydrophobic glass substrates to investigate the effect of the interactions between the particles and the substrate surface on the resultant layer structures. When the PVBTA-grafted silica particle (PVBTA-Si) was used, the colloidal monolayers with a non-close-packed (NCP) structure were formed on both hydrophilic and hydrophobic glass substrates, where the NCP colloidal layers on the hydrophobic glass substrate have a somewhat more ordered structure than those on the hydrophilic glass substrate. In the case of the PSSS-grafted silica particle (PSSS-Si), on the other hand, stripe patterns with close-packed (CP) colloidal layers were obtained on both types of the glass substrates. The number of layers of the stripes on the hydrophilic glass substrate was less than that on the hydrophobic glass substrate, while the spacing and width of the stripes on both substrates were similar to each other. The difference in the structures of the colloidal layers obtained here indicates that an attractive interaction, such as an electrostatic attraction and a hydrophobic interaction, between the particle and the substrate surface is necessary to achieve the NCP structure by the CSA process using polyelectrolyte-grafted silica particles.

Behavior of enzymatic membranes under pressure: Effect of enzyme location

Enzyme immobilized membranes combine catalysis and separation functions. Their application in large-scale continuous processes requires knowing the behavior under pressure. Also, the effects of enzyme location on the mass transfer limitation, membranes’ stability, and filtration performance should be investigated. In this study, urease (URE) and trypsin (TRY) enzymes were physically immobilized in/on the surface of a polyacrylonitrile (AN69) membrane through layer-by-layer (LbL) self-assembly method using polyethylenemine (PEI) and sodium-alginate (ALG) as cationic and anionic polyelectrolytes respectively. URE, located on the membrane’s surface, degraded urea in a reaction-controlled regime, and its immobilization did not significantly change the hydraulic permeability. On the other hand, the TRY enzyme attached to the membrane’s pores reduced the permeability and degraded the BAPNA in a diffusion-controlled region. In TRY immobilized membranes, the conversion increased linearly with the transmembrane pressure, while in URE immobilized ones, conversion was maximum at 1 bar. Sandwiching the enzymes between two polyelectrolytes resulted in the highest catalytic activities. This configuration maintained most of the URE activity in the long-term filtration, but it did not help prevent TRY’s activity loss.

X-ray structural study of membranes based on Na-CMC and CS-Cl for water purification

The level of environmental pollution is increasing year by year. Solving this problem requires the development and application of new effective technologies and materials for wastewater treatment and processing of accumulated waste. One of the alternative directions is membrane technologies, in particular, the development of biodegradable nanocomposite membranes. Anionic polyelectrolyte – Na-carboxymethyl cellulose with molecular weight Mw ~ 90000 and cationic polyelectrolyte – low molecular weight chitosan were used to create these membranes. Polymeric membranes were formed by mixing aqueous solutions of chitosan hydrochloride and Na-carboxymethylcellulose in different ratios. Analysis of X-ray diffractograms of polyelectrolyte complexes showed that with a gradual increase in the content of cationic polyelectrolyte from 5 % to 17 %, the structure of polyelectrolyte complexes changes dramatically. Whereas, the diffractograms of polyelectrolyte complexes with chitosan content from 29 % to 84 % are similar. The effectiveness of the obtained membranes was tested on a barometric device at different pressures. It was established that membranes based on polyelectrolyte complexes with a stoichiometric ratio of anionic and cationic polyelectrolytes turned out to be the most productive. The degree of water purification was checked by indicators of color selectivity. The obtained results allow us to conclude that with an increase in the duration of purification, the selectivity increases

Dual templated-based synthesis of smart zeolites and its self-healing anticorrosion coatings

The process for the synthesis of smart zeolite is complex. The porous zeolite was synthesized by a hydrothermal route. Aluminium powder and tetraethyl orthosilicate (TEOS) are used as alumina and silica sources. The presence of tetrapropylammonium hydroxide (TPAH) and sodium dodecyl benzene sulphonic acid (SDBS) acts as a structural directing agent and soft templates. The chemical growth mechanism of porous zeolite to form needle structures with the help of templates is discussed. The porous zeolite was prepared using optimum crystallization conditions (temperature and duration) and Si/Al component ratios. Following calcination, the porous zeolite was loaded with mercaptobezothaizole (MBT) and layer by layer (LBL) covered with both cationic and anionic polyelectrolytes. This is the first time a study has been conducted that embraces the porous zeolite pre-loaded with a corrosion inhibitor (MBT). Here, the MBT is released in high pH conditions to prevent corrosion, simultaneously increasing the life of the smart zeolite coatings in a corrosive environment. The smart zeolite-based coatings prevent corrosion by the pH activity of smart zeolite above the neutral pH condition.

Ultrathin Ambipolar Polyelectrolyte Capacitors Prepared via Layer-by-Layer Assembling.

Miniaturized solid state capacitors leveraging migration of unipolar ions in a single polyelectrolyte layer sandwiched between metal electrodes, namely, polyelectrolyte capacitors (PECs), have been recently reported with areal capacitance up to 100-200nF mm-2. Nonetheless, application of PECs in consumer and industrial electronics has been hindered so far by their small operational frequency range, up to a few kHz, due to the resistive behavior (phase angle >-45°) of PECs in the range kHz-to-MHz. Here,it is reported on multilayer polyelectrolyte capacitors (mPECs) that leverage as dielectric an ambipolar nanometer-thick (down to 10nm) stack of anionic and cationic polyelectrolytes assembled layer-by-layer between metal electrodes to eliminate the resistive behavior at frequencies from kHz to MHz. This significantly extends the operational range of mPECs over PECs. mPECs with areal capacitance as high as 25nF mm-2 at 20Hz and full capacitive behavior from 100 mHz to 10MHz are demonstrated using different assembling conditions and anionic/cationic polyelectrolyte pairs. The mPECs reliably operate over time for >300 million cycles, at different biasing voltages up to 3V, and temperatures up to 80°C, showing a reversible capacitive behavior without significant hysteresis. Application of mPECs in flexible electronics, also operating at high frequency, is envisaged.

Green industry work: production of FeCl3 from iron and steel industry waste (mill scale) and its use in wastewater treatment

Mill scale (MS) is considered to be a significant metallurgical waste, but there is no economical method yet to utilize its metal content. In this study, which covers various processes in several stages, the solution of iron in MS, which is the Iron and Steel Industry (I&SI) waste, as FeCl3 (MS-FeCl3) in the thermoreactor in the presence of HCl, was investigated. In the next step, the conditions for using this solution as a coagulant in the treatment of I&SI wastewater were investigated using the jar test. The results of the treated water sample were compared by chemical oxygen demand (COD), total suspended solids (TSS), color, and turbidity analyses using commercial aluminum sulfate (Al2(SO4)3) and FeCl3 (C-FeCl3). Additionally, heavy metal analyses were conducted, and the treatment performance of three coagulants was presented. Accordingly, while 2.0 mg/L anionic polyelectrolyte was consumed at a dosage of 4.05 mg/L Al2(SO4)3 at pH 7.0, 0.25 mg/L anionic polyelectrolyte was consumed at a dosage of 1.29 mg/L at pH 5.0 in the C-FeCl3 and MS-FeCl3 studies. Also, Fe, Cr, Mn, Ni, Zn, Cd, Hg, and Pb removal efficiencies were over 93.56% for all three coagulant usage cases. The results showed that the wastewater treatment performance of MS-FeCl3 by the recycling of MS, which is an I&SI waste, was at the same level as C-FeCl3. Thus, thanks to recycling, waste scale can be used as an alternative to commercial products for green production.Graphical abstract

Effect of a nonionic surfactant and anionic polyelectrolyte binary system on the stability of a calcium and magnesium carbonates dispersion

The effect of sodium polyacrylate, polyethylene glycol of various molecular weights, and their mixtures on the dispersion stability of calcium and magnesium carbonates was studied. It was shown that in the presence of a binary system, the light transmission of the dispersion decreases 1.2–1.5 times, the content of fine fraction particles increases by 1.1–1.3 times compared to the individual components. The stability of the dispersion of carbonates depends on the components ratio in the binary system and their molecular weight. The formation of adsorption solvated layers of polyacrylate and polyethylene glycol molecules at the interphase boundary contributes to an increase in the stability of the carbonate dispersion.

Treatment of effluents from Food Services Establishment (FSEs) by physico-chemical processes: a case study for Trinidad & Tobago

BackgroundEffluents from Food Services Establishments (FSEs) contain primarily Fats, Oil and Grease (FOG) which severely impact on sewers and the environment when released in high concentrations. In Trinidad & Tobago, it is estimated that approximately 231,304 kg/day of unaccounted for FOG bearing wastewaters from FSEs, are released into the environment with no viable treatment in the country. This research explored the optimization of physico-chemical processes for the treatment of FOGs for subsequent release into sewers.ResultsBench-scale studies analysed the characteristics of FSE’s effluents from three popular sources, conducted the treatment of these effluents using Jar Tests, and subsequently confirm results via a pilot plant study. Characterization showed the mean concentration of the parameters examined to be; FOG (511 mg/l ± 116 mg/l), Suspended Solids (446 mg/l ± 146 mg/l), Chemical Oxygen Demand (2229 mg/l ± 963 mg/l) and pH (6 ± 0.3). Jar Tests were conducted using Poly-aluminium Chloride (PACl) as coagulant, anionic and cationic polyelectrolytes as flocculant aids with suitable pH adjustments of samples to determine the isoelectric point for the coagulant. Effluent results showed FOG removal levels of 99.9% and final effluent concentration of 0.17 mg/l. This was attained using PACl concentration of 250 mg/l, a 0.1% low cationic polyelectrolyte (CP 1154) at 4 mg/l with the pH of sample adjusted to 8. The pilot plant achieved a 97.4% removal of FOG (residual of 16.8 mg/l) using the same coagulant dosing, and pH value, but increasing the strength of the flocculant aid to 0.1% medium cationic (CP1156) at 5 mg/l.ConclusionExperimentation showed high concentrations of emulsified FOG can be efficiently removed to levels below the permissible requirements (20 mg/l) for entry into sewer systems in Trinidad and Tobago using coagulation, flocculation and sedimentation techniques. Pilot scale study also revealed that a higher strength and/or dose of the cationic polyelectrolyte and increased times in primary and final tanks were required to attain the desired results as in the bench level study, where equipment limitations in the flocculation tank were faced. This is in alignment with theory where factors critical for agglomeration is equipment type and density charge. It is, concluded that the optimum combination of chemicals and the respective dosages attained at the bench level study should prove effective should the right equipment be made available.