Optimization of polymerization conditions and thermal degradation of conducting polypyrrole coated polyester fabrics

PET fabric is coated with conducting polypyrrole (PPy) by oxidative polymerization from an aqueous solution of Py using ferric chloride hexahydrate (FeCl₃) as oxidant and p-toluene sulphonate (pTSA) as dopant. The optimum concentrations for Py, FeCl₃ and pTSA were found to be 0.11, 0.857 and 0.077 mol/l respectively, which yielded a conductive fabrics with resistivity as low as 72 Ω/sq. PPy fabric gained resistivity less than one order of magnitude when aged for 18 months at room temperature. The stabilizing effect of the dopant pTSA against thermal degradation was demonstrated; the undoped samples reached resistivity of around 40 kΩ, whereas doped samples reached less than 2 kΩ at the same temperature and time.     

Aging studies on conducting polypyrrole

Change of tensile properties, electrical conductivity and microwave shielding of electrochemically synthesized polypyrrole films with time are presented. Highly doped films had good electrical stability, retaining high microwave reflectivity throughout the aging period. Lightly doped films were less stable and partially reflective and absorptive of microwaves. FT-IR spectral observations revealed a progressive increase in intensity of an unsaturated conjugated carbonyl peak, which was not observed in the highly doped films, suggesting that the concentration of the dopant had an influence on the mechanism of degradation of conductivity.     

Structural investigation of anionic functional poly(vinyl alcohol) doped polypyrrole nanospheres

This article reports on a facile route for the preparation of polypyrrole nanospheres with improved water solubility, ordering and conductivity in the presence of a polyelectrolyte, such as phosphorylated polyvinyl alcohol. The phosphorylated polyvinyl alcohol (PPVA) was used as both the stabilizer and the dopant in the chemical oxidative polymerization of pyrrole. The resulting PPVA doped polypyrrole (PPy) nanocomposites (PPy-PPVA) were characterized with FTIR, TGA, SEM and AFM techniques. The electrical conductivity of polymer was measured by four-point probe method. Our observation and results suggest a plausible formation mechanism of PPy nanospheres, PPVA micelle might have functioned as ‘template’ during the polymerization of pyrrole monomers, meanwhile, the PPy chains doped with phosphate group. It was found that the size decreased and their dispersion stability in water increased with the increasing feeding ratio of PPVA. The conductivity of PPy with different morphologies was also measured and compared. When the PPVA: pyrrole feeding ratio ranged from 20 to 50 wt%, the PPy-PPVA nanoparticles showed spherical shape with excellent uniformity, good electrical conductivity (up to 33.1 S·cm^?1), and weakly temperature dependent conductivity. It’s worth mentioning that the PPy-PPVA nanocomposite prepared in high PPVA feeding ratio has been well-dispersed for more than 24 months, which indicates its significant dispersion stability.     

Synthesis and characterization of electrically conductive composite films of polypyrrole/poly(acrylonitrile-co-styrene)

Homogeneus Polypyrrole (PPy)/poly(acrylonitrile-co-styrene) (SAN) composite thin films were prepared by chemical polymerization of pyrrole on poly(acrylonitrile-co-styrene) matrix. Ce (IV) is used as an oxidant for in-situ polymerizion of pyrrole on SAN matrix, having an advantageous over the impregnation method. The formation and incorporation of PPy in the copolymer matrix were confirmed by FTIR-ATR and UV-Visible spectrophotometric measurements. Thermal analyses showed that after polymerization of Py in copolymer matrix, thermal behavior of SAN was changed and derivative of weight loss at this temperature was increased by increasing of PPy content. XPS and FTIR-ATR analysis of composite films indicated cerium salt with nitrate ion acted as a dopant. The increase in the AC electrical conductivity of the PPy/SAN composites over pure SAN was observed. At lower frequency up to 10⁵ Hz, conductivity was shown an independent behavior from frequency; but at high frequencies (10⁵–10⁷ Hz), dependence on frequency was explained by polaron and bipolaron formations of PPy. The dispersion of PPy particles in copolymer matrix was proven by SEM, AFM and digital camera. By the increase of PPy content in the composite films, increase in AC conductivities, and decrease in dielectric constants and loss were observed.     

Preparation of the Multicomponent High Temperature Proton Exchange Membranes with Layer by Layer Self-assembly Technique

Layer by layer (LBL) self-assembly technique has been proved to be a feasible method that enables to accomplish the preparation of functional membranes with multilayered structure. In this research, the polymer of sulfonated polyetheretherketone (SPEEK) and thioglycolic acid capping of cadmium telluride (CdTe) nanocrystals as polyanion, the polymer of polyurethane (PU) as polycation have been used to prepare membrane electrolytes. These multilayered membranes showed good thermal stability and exhibited low liquid methanol permeability, which provided a possibility for the prepared membranes as proton exchange membranes (PEMs) to apply in direct methanol fuel cells (DMFCs). We have also demonstrated that the multicomponent (SPEEK/PU/CdTe/PU)₁₀₀ membranes favored to combine more phosphoric acid (PA) molecules and possessed a higher proton conductivity comparing to the bicomponent (SPEEK/PU)₂₁₀ membranes. So PA doped (SPEEK/PU/CdTe/PU)₁₀₀ membrane presented a maximum proton conductivity up to 8.6×10^-2 S/cm at 160 °C under anhydrous conditions. However, PA doped (SPEEK/PU)₂₁₀ membranes underwent a drop on proton conductivity while the temperature exceeded 120 °C.     

Effect of conformation on the properties of uniaxially drawn polylacide films upon drawing temperature

Polylactide(PLA) films were drawn at various drawing temperature of 65, 90 and 120 °C. The effects of drawing temperature on structural conformation and properties of PLA films were investigated. It was confirmed that the PLA films at drawing temperature of 65 and 90 °C were composed of α′ phase crystal form. The strain-induced crystallization and molecular orientation increased with increasing the draw ratio, which result in improving the mechanical and thermal properties of α′ phase PLA films. However, at drawing temperature of 120 °C, the strain-induced crystallization and molecular orientation of PLA films were not distinctly detected. It was supposed that the rate of the chain relaxation was faster than chain orientation and strain-induced crystallization during uniaxial drawing process.     

Synthesis and characterization of boron doped alumina stabilized zirconia fibers

Boron doped PVA/Zr-Al acetate nanofibers were prepared by electrospinning using PVA as a precursor. The effect of calcination temperature on morphology and crystal structure was investigated at 250, 500, and 800 °C. The study also establishes the effect of boron doping on the morphology of PVA/Zr-Al acetate nanofibers at various calcination temperatures. The measurements showed that the conductivity, pH, viscosity and the surface tension of the hybrid polymer solutions have increased with boron doping. In addition, the fibers were characterized by FTIR, DSC, XPS, XRD and SEM techniques. The addition of boron did not only increase the thermal stability of the fibers, but also increased the average fiber diameters, which gave stronger fibers. The DSC results indicated that the melting temperature (Tm) of the fibers was increased from 256 to 270 °C with the addition of boron. XRD peak patterns showed that after further heat treatment at 800 °C, zirconia exists in two phases of tetragonal and monoclinic modifications. Moreover, alumina does not transform into the γ-Al₂O₃ and θ-Al₂O₃ phase at 800 °C. The SEM appearance of the fibers showed that the addition of boron resulted in the formation of crosslinked bright surfaced fibers.     

Effect of temperature on germination and early growth of subterranean clover, capeweed and Wimmera ryegrass

Germination of annual pasture species was studied under controlled‐environment conditions in south‐western Australia at temperatures in the range from 4°C to 35°C. Subterranean clover (Trifolium subterraneum) and Wimmera ryegrass (Lolium rigidum) had a germination of 90% between 12°C and 29°C, whereas capeweed (Arctotheca calendula) had a high germination percentage in a much narrower temperature range with an optimum of 25°C. Growth of subterranean clover, capeweed and Wimmera ryegrass between 28 and 49 days after sowing (DAS) was also studied at two photon flux densities, 13 and 30 mol m^?2 d^?1, and at diel temperatures in the range from 15/10°C to 33/28°C. Pasture species grown at a density of 1000 plants m^?2 accumulated at least twice the amount of shoot dry matter when subjected to temperatures of 21/16°C and 27/22°C, compared with a lower temperature of 15/10°C and a higher temperature of 33/28°C. Except at the highest temperature and at high photon flux density, capeweed had lower green area indices (GAI) than the other two species at 28 DAS. Crop growth rates between 28 and 49 DAS were higher in Wimmera ryegrass than in the other two species, whereas subterranean clover had a lower relative growth rate than the other two species at all temperatures and both photon flux densities. Subterranean clover and capeweed intercepted a greater proportion of the incident radiation compared with Wimmera ryegrass. The values of radiation interception and GAI were used to estimate the number of DAS to reach 75% radiation interception [f_(0·75)]. The number of days to reach f_(0·75) decreased with increasing temperature from 15/10°C to reach a minimum at 27/22°C. The time taken to achieve f_(0·75) was always shorter by about 10 d when the photon flux density was 30 mol m^?2 d^?1 in the autumn compared with 13 mol m^?2 d^?1 in the winter. These results are discussed in relation to the early growth of annual pasture in the field.     

Yield and nutritive value of timothy as affected by temperature,photoperiod and time of harvest

Scenarios of global climate change forecast an increase in air temperature of 3°C over the next 100 years in eastern Canada. Growth and nutritive value of cool‐season grasses are known to be affected by air temperature. It is also believed that grasses grown at high latitude have a greater nutritive value. The objectives of this study were to assess the effect of four combinations of day/night temperature and photoperiod (15 h–17/5°C; 15 h–22/10°C; 15 h–28/15°C; and 17 h‐17/5°C) on dry‐matter (DM) yield, in vitro true DM digestibility (IVTD), in vitro digestibility of neutral‐detergent fibre (NDF), and concentrations of NDF, acid‐detergent fibre (ADF), lignin, minerals and non‐structural carbohydrates (NSC) in timothy grown under controlled conditions. Furthermore, herbage was harvested in the morning and in the afternoon to assess the impact of the time of harvest. The dietary cation–anion difference [DCAD = (K⁺ + Na⁺) ? (Cl^? + 0·6 S^2?)] and the grass tetany index [GT index = K⁺/(Ca²⁺ + Mg²⁺)] were also calculated. Higher temperature regimes significantly decreased IVTD and digestibility of NDF but had a limited effect on concentrations of NDF, ADF and lignin. DM yield of herbage was less and the concentration of NSC was greater in timothy grown under a temperature regime of 28/15°C than the 17/5°C and 22/10°C regimes; this effect is mainly explained by a response to temperature stress. Values of DCAD and the GT index of herbage were also lower under the 28/15°C than the 17/5°C and 22/10°C regimes as a result of a decreased plant K concentration. Under the 17/5°C regime, an increase in 2 h of photoperiod resulted in increased DM yield, decreased concentrations of K, Ca, Mg, Cl and N, and an increased starch concentration; IVTD or digestibility of NDF were not affected, although lignin concentration was reduced. Harvesting timothy in the afternoon rather than in the morning resulted in higher NSC, mainly sucrose, concentrations, and decreased ADF and NDF concentrations. The forecasted increase in air temperature in eastern Canada over the next 100 years will result in lower yields and nutritive value of timothy.     

Reinforcement of wet milled jute nano/micro particles in polyvinyl alcohol films

Textile industry generate significant amount of waste fibres in form of short lengths during mechanical processing. However these short fibres possess excellent properties suitable for many other applications. The objective of this work was to use them for the preparation of nanoparticles/nanofibres as fillers in biodegradable composite applications such as food packaging, agriculture mulch films, automotive plastics, etc. The present paper concerns with jute fibres as a source of nanocellulose for reinforcement of PVA mulch films. Jute fibres were first refined to micro/nanoscale particles in form of nanofibrillar cellulose (NFC) by high energy planetary ball milling process in dry and wet condition. Wet milling was observed more efficient than dry milling in terms of unimodality of size distribution with reduction in size below 500 nm after milling for 3 hours. Later the obtained particles were used as fillers in Poly vinyl alcohol (PVA) films and their reinforcement evaluated based on thermal properties. It was observed that glass transition temperature (T_g) of PVA films improved from 84.36 °C to 95.22 °C after addition of 5 % jute particles without affecting % crystallinity and melting temperature (T _m) of PVA. Dynamic mechanical analysis of composite films with 5 % jute particles showed higher value of 14×10⁸ Pa for storage modulus in comparison to 9×10⁸ Pa of neat composite film. The percolation effect was observed more above glass transition temperature which consequently resulted in improved transfer of stiffness from jute particles to PVA matrix above 50 °C. The percolation phenomena also explained the improvement in thermal stability by 10 °C for every increased loading of jute particles due to formation of hydrogen bonds with PVA matrix.     

Modelling net photosynthetic rate of field-grown cocksfoot leaves under different nitrogen, water and temperature regimes

A simple multiplicative model using temperature, foliage nitrogen (N) concentration and water status was developed to predict the maximum photosynthetic rate (Pmax) of field‐grown cocksfoot (Dactylis glomerata L.) leaves when none, one, two or all the factors were limiting. The highest Pmax was 27·4 μmol CO₂ m^–2 s^?1 in non‐limited conditions, which was defined as the standardized Pmax value dimensionless (Pmax_s=1). Pmax_s increased 0·058 units per °C from 10°C to the optimum range (19–23°C) (Pmax_s=1) and then declined 0·077 units of Pmax_s per °C from 23 to 31°C. Pmax_s=1 was also measured from 59 to 52 g N kg^?1 dry matter (DM) foliage N. Pmax_s then decreased at the rate of 0·115 units per 10 g N kg^?1 DM from 52 to 26 g N kg^?1 DM, and 0·409 units of Pmax_s per 10 g N kg^?1 DM from 26 to 15 g N kg^?1 DM. For predawn leaf water potential (ψ_lp), Pmax_s=1 was measured from ?0·1 to ?1·2 bar but declined linearly at a rate of 0·078 units per bar of ψ_lp from ?1·2 to ?14·0 bar because of a linear decrease in stomatal conductance. An interaction between low N content (≤20 g N kg^?1 DM) and high temperature (>23°C) was also detected. Together, this multiplicative model accounted for 0·82 of the variation in Pmax_s.     

Top spoilage losses in maize silage sealed with plastic films with different permeabilities to oxygen

The quality of plastic films used for horizontal silos is important to limit losses in the upper silage layer. The aim of this work was to study the effectiveness of different plastic films in reducing the top losses in maize silage. The following treatments were evaluated: (i) coextruded polyethylene/polyamide oxygen barrier film (OB), (ii) polyethylene film (PE), (iii) polyvinyl chloride film (PVC), and (iv) coextruded PE/polyvinyl alcohol film (PVOH). These treatments differed according to oxygen permeability with values of 75, 722, 982 and 289 cm³ m^?2 per 24 hour respectively. OB and PVOH films had better temperature and fermentation profiles than the more permeable films. The OB film was effective in reducing the dry‐matter (DM) losses during storage (82 g kg^?1), and the PVOH film had an intermediate value of DM loss (101 g kg^?1). PE and PVC films had higher losses (138 and 145 g kg^?1 respectively). Oxygen permeability of the films promoted a positive correlation with DM losses (P < 0·05; r² = 0·945). The results indicate that O₂ permeability through the plastic film is a crucial factor for maintaining silage quality in the upper layer of the silo when it is perfectly sealed.     

Shelf life study of some Nigerian fruit juices inoculated with ascospores ofNeosartorya spp.

Mango, orange and pineapple juices containing various concentrations of sucrose were dispensed in 100 ml volumes into 100 ml conical flasks with stoppers. Each juice in a flask was inoculated with ascospores of one local isolate of eitherNeosartorya fischeri, N. fischeri var.spinosa orN. quadricincta to a final concentration of 120–140 ascospores/ml of juice, and then pasteurized at 80°C for 30 min. A set of 36 inoculated flasks with 12 controls was stored at 4–5°C and two sets, one protected with 100 mg/l sodium benzoate, were stored at room temperature (25–28°C). A shelf life study was carried out on all the juices for 64 days. Only fruit juices stored at 4–5°C and those containing sodium benzoate stored at room temperature were protected from spoilage by these fungi for 64 days. Addition of sucrose at levels of 9% to mango juice, 30% to pineapple juice and 31.5% to orange juice significantly (p=0.05) protected ascospores from inactivation during cold storage.     

High Antioxidant Activity Mixture of Extruded Whole Quality Protein Maize and Common Bean Flours for Production of a Nutraceutical Beverage Elaborated with a Traditional Mexican Formulation

The objective of this study was to determine the best combination of extrusion process variables for the production of whole quality protein maize (EQPMF) and common bean (ECBF) flours to prepare a high antioxidant activity mixture (EQPMF + ECBF) suitable to produce a nutraceutical beverage with high acceptability elaborated with a traditional Mexican formulation. Processing conditions were obtained from a factorial combination of barrel temperature (BT?=?120–170 °C) and screw speed (SS?=?120–200 rpm). Response surface methodology was applied to obtain maximum values for antioxidant activity (A _ox A) of the flour mixture (EQPMF + ECBF) and acceptability (A) of the nutraceutical beverage. The best combinations of extrusion process variables for EQPMF and ECBF to prepare an optimized mixture (60%EQPMF?+?40%ECBF) were BT?=?98 °C/SS?=?218 rpm and BT?=?105 °C/SS?=?83 rpm, respectively. The optimized mixture had A _ox A?=?14,320 μmol Trolox equivalent (TE)/100 g sample dry weight (dw) and a calculated protein efficiency ratio (C-PER) of 2.17. A 200 ml portion of a beverage prepared with 25 g of the optimized flour mixture had A _ox A?=?3,222 μmol TE, and A?=?89 (level of satisfaction “I like it extremely”). This nutraceutical beverage could be used as an alternative to beverages with low nutritional/nutraceutical value, such as those prepared with water, simple sugars, artificial flavoring and colorants, which are widely offered in the market.     

Nano-TiO<Subscript>2</Subscript> based multilayer film deposition on cotton fabrics for UV-protection

Nano-TiO₂ based multilayer nanocomposite films were fabricated on cationically modified woven cotton fabrics by layer-by-layer molecular self-assembly technique. Cationization process was used to obtain cationic surface charge on cotton fabrics. Attenuated total reflectance Fourier transform infrared spectroscopy analyses were used to verify the presence of cationic surface charge and multilayer films deposited on the fabrics. Scanning electron microscope micrographs of poly(sodium 4-styrene sulfonate)/TiO₂, nano polyurethane/TiO₂, and TiO₂/poly(diallyldimethylammonium chloride) multilayer films deposited on cotton fabrics were taken. With nano-TiO₂ based multilayer film deposition, the protection of cotton fabrics against UV radiation is enhanced. The UV protection durability of the self-assembled multilayer films deposited on the cotton fabrics was analyzed after 10 and 20 washing cycles at 40 °C for 30 min. Air permeability and whiteness value analysis were performed on the untreated and multilayer film deposited cotton fabrics. The effect of layer-by-layer deposition process on tensile strength properties of the warp and weft yarns was determined.     

A comparison, under controlled environmental conditions, of a Lolium multiflorum selection bred for high dry-matter content and non-structural carbohydrate concentration with a commercial cultivar

Abstract The nutritional value of Italian ryegrass (Lolium multiflorum) selection 121, bred for a high dry‐matter content and a high concentration of total non‐structural carbohydrate (TNC), was compared with that of Westerwolds ryegrass (L. multiflorum ssp. Westerwoldicum) cv. Midmar in a controlled environment. The concentration of neutral‐detergent fibre (NDF), acid‐detergent fibre (ADF), acid‐detergent lignin (ADL), nitrogenous compounds, minerals and in vitro digestibility were investigated as characteristics of nutritive value. The anatomical features of selection 121 and the Midmar cultivar were studied to determine possible structural differences. Thirty pots each of selection 121 and Midmar containing four plants per pot were arranged in a randomized block design in a controlled environment chamber. There were two temperature regimes during the study, the first being a warm regime (30 °C/20 °C) for 7 weeks followed by a cold regime(20 °C/7 °C) of a further 7 weeks. In the warm regime, the dry‐matter (DM) content and the TNC concentration of selection 121 were 0·17 and 0·16 higher, respectively, than Midmar. The NDF concentration was significantly (P < 0·01) higher in Midmar than in selection 121. When grown under warm conditions, Midmar had significantly (P < 0·001) higher concentrations of Mg, K, Na and Mn than selection 121. In the cold regime, the DM content and TNC concentration of selection 121 were 0·25 and 0·22 higher, respectively, than Midmar. No significant differences in the anti‐quality factors investigated were found between the two ryegrasses. In the cold regime, Midmar had significantly (P < 0·001 and P < 0·01) higher Ca, Mg, K, Na, Zn, Mn and P concentrations than selection 121. The results from this controlled environment study suggest that selection 121 is superior to Midmar in terms of the quality characteristics DM and TNC, and that these characteristics are not positively linked to anti‐quality factors associated with forage species.     

Thermodynamics of adsorption of laccaic acid onto chitosan and associated dye toxicity studies

The thermodynamics of adsorption of laccaic acid (lac dye) onto chitosan were investigated under acidic condition over various concentrations (20–293 mg/l). Langmuir, Freundlich, and Temkin isotherms were used to analyze the equilibrium data at different temperatures, with the Freundlich isotherm fitting the experimental data significantly better than the other isotherms. The effect of temperature on the adsorption isotherm was studied by carrying out a series of isotherms at 10, 20, 40, and 60 °C. It was found that more dye was strongly adsorbed by chitosan when the temperature of the dye solution increased. Thermodynamic parameters such as free energy change (ΔG°), enthalpy change (ΔH°), and entropy change (ΔS°) were also evaluated. The negative value of ΔG° and positive value of ΔH° indicated that the laccaic acid adsorption process is a spontaneous and an endothermic one. Attenuated total reflectance Fourier transform infrared spectroscopy confirmed the functional groups of chitosan that affected the laccaic acid adsorption. Therefore, laccaic acid molecules could interact with the chitosan via electrostatic forces, hydrogen bonding, and ion-dipole interactions under acidic condition. From the toxicity study, the dye solution with the initial dye concentrations of 40 and 120 mg/l before dye removal showed significant mortality to earthworm Diplocardia communis (P<0.01).     

Properties and performance of polypyrrole (PPy)-coated silk fibers

Different silk substrates in form of spun silk tops, nonwoven web, yarn, and fabric were coated with electrically conducting doped polypyrrole (PPy) by in situ oxidative polymerization from an aqueous solution of pyrrole (Py) at room temperature using FeCl₃ as catalyst. PPy-coated silk materials were characterized by optical (OM) and scanning electron (SEM) microscopy, FT-IR spectroscopy, and thermal analysis (DSC, TG). OM and SEM showed that PPy completely coated the surface of individual silk fibers and that the polymerization process occurred only at the fiber surface and not in the bulk. Dendrite-like aggregates of PPy adhered to the fiber surface, with the exception of the sample first polymerized in the form of tops and then spun into yarn using conventional industrial machines. FT-IR (ATR mode) showed a mixed spectral pattern with bands typical of silk and PPy overlapping over the entire wavenumbers range. DSC and TG showed that PPy-coated silk fibers attained a significantly higher thermal stability owing to the protective effect of the PPy layer against thermal degradation. The mechanical properties of silk fibers remained unchanged upon polymerization of Py. The different PPy-coated silk materials displayed excellent electrical properties. After exposition to atmospheric oxygen for two years a residual conductivity of 10–20 % was recorded. The conductivity decreased sharply under the conditions of domestic washing with water, while it remained essentially unchanged upon dry cleaning. Abrasion tests caused a limited increase of resistance. PPy-coated silk tops were successfully spun into yarn either pure or in blend with untreated silk fibers. The resulting yarns maintained good electrical properties.     

Water vapor transport parameters of a cast wheat gluten film

Understanding the mode of transport of water vapor through the film is important for improving the moisture barrier properties of wheat gluten (WG) films. Effective permeability (P_eff), solubility (S_eff), and diffusion (D_eff) coefficients of a hydrophilic cast WG film were determined at 25°C within the relative humidity (RH) range of 0–84% (with a 9–13% RH gradient between upstream and downstream water vapor flux). P_eff, S_eff, and D_eff increased substantially as the RH gradient moved upwards in the RH spectrum. P_eff increased by four orders of magnitude from the lowest RH condition of 0–11% (3.8×10⁻¹¹ g·m/m²·s·Pa) to the highest RH condition of 75–84% (4.1×10⁻⁷ g·m/m²·s·Pa). A moisture sorption isotherm of the film at 25°C was constructed. Both the Guggenheim–Anderson–DeBoer (GAB) and the Kuhn moisture sorption isotherm models showed a good fit to the experimental adsorption data. Testing of WG films at the expected conditions of actual use is necessary to quantify the water vapor permeation through the films.     

Improvement of mechanical and electrical properties of poly(ethylene glycol) and cyanoresin based polymer electrolytes

Ionic conductivity and mechanical properties of a mixed polymer matrix consisting of poly(ethylene glycol) (PEG) and cyanoresin type M (CRM) with various lithium salts and plasticizer were examined. The CRM used was a copolymer of cyanoethyl pullulan and cyanoethyl poly(vinyl alcohol) with a molar ratio of 1:1, mixed plasticizer was ethylene carbonate (EC) and propylene carbonate (PC) at a volume ratio of 1:1. The conductive behavior of polymer electrolytes in the temperature range of 298∼338 K was investigated. The PEG/LiClO₄ complexes exhibited the highest ionic conductivity of ∼10⁻⁵ S/cm at 25°C with the salt concentration of 1.5 M. In addition, the plasticized PEG/LiClO₄ complexes exhibited improvement of ionic conductivity. However, their complexes showed decreased mechanical properties. The improvement of ionic conductivity and mechanical properties could be obtained from the polymer electrolytes by using CRM. The highest ionic conductivity of PEG/CRM/LiClO₄/(EC-PC) was 5.33×10⁻⁴ S/cm at 25°C.