Polymer Blends Research Articles

Effect of Additives on Thermal Degradation and Crack Propagation Properties of Recycled Polyethylene Blends.

Additives, such as antioxidants (AOs), carbon black (CB) and compatibilizers (COs), are used in recycled polymer blends for different reasons. AOs slow thermal degradation, CB gives blends a black color and protect them against ultraviolet (UV) light, and compatibilizers improve compatibility between the different phases of the mixture and consequently enhance the mechanical properties of the final blend. In this paper, the three additives were added to recycled polyethylene (PE) blends to study their effect on the final properties and to determine the best formulations that help improve the mechanical properties of recycled PE blends. Stress Crack Resistance (SCR) was accessed by performing Notched Crack Ligament Stress (NCLS) and Un-notched Crack Ligament Stress (UCLS). On the other hand, Oxidative Induction Time (OIT) was used to determine the oxidation time of the blends and the effect of each additive on this property. Based on the results of this study, it was proven that adding carbon black and antioxidants delay the thermal degradation of recycled PE blends and consequently improve the OIT. Otherwise, resistance to stress cracking is improved only by adding a compatibilizer to the reference blend.

Characterization of 4D printed shape memory and conventional polymer blends for thermal responsive applications

Characterization of 4D printed shape memory and conventional polymer blends for thermal responsive applications

Enhanced Physio‐Chemical Properties of PMMA/PS Polymer Blends by DC Glow Discharge Plasma Treated K2TI6O13 for Electronic Applications

AbstractCeramic filler modified polymer blends are more in demand due to their excellent compatibility, easy processing and cost‐effectiveness. In the present work, we modified Polymethyl methacrylate (PMMA)/Polystyrene (PS) blends using solution blending with untreated (UT) and DC glow discharge plasma‐treated (air plasma treated‐APT) potassium hexatitanate (K2Ti6O13). Chemical bonding of virgin and modified blends was confirmed by Fourier transform infrared spectrophotometer (FTIR). Decreased structural defects and imperfections of KTO were confirmed by Raman spectroscopy. Modified surface morphology and elemental analysis were detected by scanning electron microscopy (SEM) and energy‐dispersive X‐ray analysis (EDAX). The quantification of particle size distribution has been determined by Zetasizer. Increased degree of crystallinity and decreased average crystallite size after plasma treatment were determined by X‐ray diffraction. Increased dielectric constant from ~22–200 and decreased loss up to 0.7 were analyzed by impedance analyzer. Lee's disc probe was deployed to confirm the optimized thermal conductivity of the modified blend system. By Differential Scanning Calorimetry, glass transition temperature of modified polymer blends was investigated. The change in surface from hydrophobic to hydrophilic by plasma exposure was confirmed by surface goniometer. However, the enhanced dielectric performance of modified PMMA/PS/KTO polymer blends may be suitable for flexible energy storage devices and gadgets.

Surface-Grafted Biocompatible Polymer Conductors for Stable and Compliant Electrodes for Brain Interfaces.

Durable and conductive interfaces that enable chronic and high-resolution recording of neural activity are essential for understanding and treating neurodegenerative disorders. These chronic implants require long-term stability and small contact areas. Consequently, they are often coated with a blend of conductive polymers and are crosslinked to enhance durability despite the potentially deleterious effect of crosslinking on the mechanical and electrical properties. Here the grafting of the poly(3,4 ethylenedioxythiophene) scaffold, poly(styrenesulfonate)-b-poly(poly(ethylene glycol) methyl ether methacrylate block copolymer brush to gold, in a controlled and tunable manner, by surface-initiated atom-transfer radical polymerization (SI-ATRP) is described. This "block-brush" provides high volumetric capacitance (120 F cm─3), strong adhesion to the metal (4h ultrasonication), improved surface hydrophilicity, and stability against 10000 charge-discharge voltage sweeps on a multiarray neural electrode. In addition, the block-brush film showed 33% improved stability against current pulsing. This approach can open numerous avenues for exploring specialized polymer brushes for bioelectronics research and application.

PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers: Improved the physical properties for energy storage devices and optoelectronic applications

The current investigation aims to enhance the optical and dielectric properties of poly (vinyl alcohol) (PVA)/polyethylene glycol (PEG) blended polymers via loading with copper cobaltite (CuCo2O4), polyaniline (PANi), and x wt% multi-walled carbon nanotubes (MWCNTs) for potential applications in optoelectronics and capacitive storage. The fabrication of PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers was carried out via casting and hydrothermal methods. Characterization of the blended polymer's structure and morphology was conducted using X-ray diffraction and scanning electron microscopy techniques. The impact of various fillers on the linear and nonlinear optical properties of the host blend was analyzed. The loaded blends demonstrated efficacy in blocking UVA, UVB, and UVC spectra, making them suitable absorbers for solar cells. The lowest values for direct and indirect optical band gap energy (Eg), of 5.34 eV and 4.44 eV were attained at x = 0.02. The blend with x = 0.01 displays the highest refractive index at λ = 600 nm. The optical conductivity exhibited nonmonotonically growth until peaking at x = 0.01. Analysis of chromaticity diagrams in CIE 1931 color space reveals that all blends emit blue-violet hues with slight variations in intensity. The fluorescence (FL) intensity of the doped blend is notably lower compared to the undoped counterparts. The doped blend (x = 0.03) showcases superior dielectric constants and ac conductivity values. The maximum energy density was achieved at 1 kHz for the host blend incorporating CuCo2O4/PANi. Overall, the observed characteristics indicate that PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers represent promising hybrid nanomaterials suitable for diverse applications.

Selenium loaded sodium alginate/polyvinyl alcohol nanocomposite film as wound dressing: structural, optical, mechanical, antimicrobial properties and biocompatibility

In the current research, synthesized Se-NPs were loaded into sodium alginate/polyvinyl alcohol SA/PVA blend, 1:2 (w:w), with different proportions to form nanocomposite films by using the solution casting method. The main goal is to enhance the physical and antibacterial properties of the polymer blend; therefore, it can be utilized for wound dressing applications. The physical aspects of the prepared films were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR), atomic force microscope (AFM), scanning electron microscope (SEM), Energy dispersive X-ray (EDX), UV–Vis spectroscopic technique, and mechanical analysis to show the effect of increasing the concentration of Se-NPs from zero to 0.5 wt% on their properties. Regarding the XRD analysis, the calculated values of lattice strain (ε\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\varepsilon$$\\end{document}) increased from 0.005 to 0.013. The FTIR absorption spectrum recorded an intensity reduction and position shift in the main characteristic peaks of SA/PVA. The morphology of Se-NPs revealed a spherical shape with a mean diameter of 131.76 nm, as revealed by transmission electron microscopy (TEM). The surface morphological images showed the appearance of a few cracks; besides, the average roughness increased from 1.59 to 2.08 nm. According to the UV–Vis spectroscopic analysis, the optical band gap reduces (from 5.425 to 5.216 eV) for the direct transition and from (5.07–4.78 eV) for the indirect transition, which is an indication of the interaction between Se-NPs and SA/PVA blend. Young’s modulus, tensile strength, and yield strength of the films increased with the addition of selenium nanoparticles. On the other hand, the amount of selenium release significantly increased with enhancing the concentration of Se-NPs in SA/PVA blend film from 0.1 to 0.5 wt%. Additionally, the inclusion of Se-NPs supplied the polymer blend with excellent antimicrobial activity, which would remove the possibility of microbial infection at the wound site. Moreover, the prepared SA/PVA/Se nanocomposite films have good biocompatibility with Human Skin Fibroblast (HSF). The results suggest the potential of this nanocomposite to be used in wound dressing applications.

The fate of post-use biodegradable PBAT-based mulch films buried in agricultural soil

The fate of black biodegradable mulch film (MF) based on starch and poly(butylene-adipate-co-terephthalate) (PBAT) in agricultural soil is investigated herein. Pristine (BIO-0) and UV-aged film samples (BIO-A192) were buried for 16 months at an experimental field in southern Italy. Visual, physical, chemical, morphological, and mechanical analyses were carried out before and after samples burial. Film residues in the form of macro- and microplastics in soil were analyzed at the end of the trial.Progressive deterioration of both pristine and UV-aged samples, with surface loss and alterations in mechanical properties, occurred from 42 days of burial. After 478 days, the apparent surface of BIO-0 and BIO-A192 films decreased by 57 % and 66 %, respectively. Burial determined a rapid depletion of starch from the polymeric blend, especially for the BIO-A192, while the degradation of the polyester phase was slower. Upon burial, an enrichment of aromatic moieties of PBAT in the film residues was observed, as well as microplastics release to soil. The analysis of the MF degradation products extracted from soil (0.006–0.008 % by mass in the soil samples) revealed the predominant presence of adipate moieties. After 478 days of burial, about 23 % and 17 % of the initial amount of BIO-0 and BIO-A192, respectively, were extracted from the soil. This comprehensive study underscores the complexity of biodegradation phenomena that involve the new generation of mulch films in the field. The different biodegradability of the polymeric components, the climate, and the soil conditions that did not strictly meet the parameters required for the standard test method devised for MFs, have significantly influenced their degradation rate. This finding further emphasizes the importance of implementing field experiments to accurately assess the real effects of biodegradable MFs on soil health and overall agroecosystem sustainability.

Structural Characterization of Pyruvic Acid Dimers Formed inside Helium Nanodroplets by Infrared Spectroscopy and Ab Initio Study.

The structural arrangements of α-keto acid complexes hold significant interest across various fields of chemistry such as enzyme modeling, drug design, or polymer blending. Herein, we report mass-selective infrared (IR) spectra of pyruvic acid monomers and dimers in the range 1720-1820 cm-1 recorded in helium nanodroplets at 0.37 K. The monomer features IR bands at 1807.1 and 1734.5 cm-1, which are assigned to the carboxylic and ketonic C═O stretching vibrations, respectively. Furthermore, the pyruvic acid dimers generated inside the helium nanodroplets are characterized by carboxylic and ketonic C═O stretch vibrations appearing at 1799.2 and 1737.0 cm-1, respectively. This frequency shift of ±7 cm-1 for both C═O stretching bands from the monomer to the dimer demonstrates that the structural motif of the monomer is maintained upon dimer aggregation in helium nanodroplets. The structural assignments were supported by a comparison of the MP2/aug-cc-pVDZ-predicted harmonic vibrational spectra at the C═O stretching region with the experiments. The global minimum monomer structure with an intramolecular hydrogen bond and its dimer stabilized by both inter- and intramolecular hydrogen bonding interactions reproduce the experimental spectra from the monomer and dimer. This assigned dimer structure lies ca.11 kJ/mol above the corresponding global minimum and is favored in helium nanodroplets due to the long-range realignment of molecules via dipole-dipole interaction, followed by short-range stabilization upon intermolecular hydrogen bond formation. The barrier for reconfiguration of the precooled monomer conformer leading to the formation of the most stable dimer structure is around 58 kJ/mol, which is infeasible at 0.37 K.

Photocatalytic hydrogen evolution on tubular shape cellulose acetate/crystalline nanocellulose/polyvinyl alcohol membranes with embedded nanocrystalline catalysts

In this work, we design an efficient and cost-effective porous membrane composed by polymeric blend that supports different photocatalytic materials. The thin (300 μm) porous photocatalytic membrane has a tubular shape and was flexible for easy handle in the reactor. The membrane is composed of a polymeric blend based on cellulose acetate, crystalline nanocellulose and polyvinyl alcohol, obtained by the phase inversion method, using cold water as non-solvent. Bismuthates (KBiO3, NaBiO3) and aluminates (ZnAl2O4 and Cu0·9Zn0·1Al2O4) powders were synthesized by diverse methodologies and were embedded into polymeric matrix. The hydrogen evolution performance of photocatalyst powders and photocatalytic composite membranes, under UV light irradiation during 180 min, were compared. The best result of hydrogen evolution was obtained by Cu0·9Zn0·1Al2O4 powders reaching 117.74 μmolg−1h−1 and the M−CuZn membrane reaching 90.07 μmolg−1h−1. The obtained results show the high potential of these polymeric membranes as a green alternative support for photocatalysts for hydrogen evolution.

3D Printable Antimicrobial Polymer Blend

AbstractThree‐dimensional (3D) printing is an innovative manufacturing method for preparing designer materials with complex geometries. However, there are very few studies on the fabrication of antimicrobial polymer materials suitable for use in everyday clinical objects, via 3D printing. In this work, an antibacterial polymer material is prepared by blending polyamide 11 (matrix), a high‐performance engineering thermoplastic, and a styrene maleimide copolymer with pendant quaternary amine moieties, and the blend 3D printed via selective laser sintering. The quaternary amine functionalities confer permanent antimicrobial properties. Blend properties are studied prior to printing via differential scanning calorimetry, powder X‐ray diffraction, and FTIR spectroscopy. Additionally, the mechanical and antimicrobial properties of the polymer blends and printed material are also assessed. The microstructure of the 3D printed polymer materials is further characterized via DOSY NMR spectroscopy. This study indicates that this is a promising approach for preparing nonleaching antimicrobial 3D printable materials.

Melt electrowriting of poly(ϵ-caprolactone)—poly(ethylene glycol) backbone polymer blend scaffolds with improved hydrophilicity and functionality

Melt electrowriting (MEW) is an additive manufacturing technique that harnesses electro-hydrodynamic phenomena to produce 3D-printed fibres with diameters on the scale of 10s of microns. The ability to print at this small scale provides opportunities to create structures with incredibly fine resolution and highly defined morphology. The current gold standard material for MEW is poly(ϵ-caprolactone) (PCL), a polymer with excellent biocompatibility but lacking in chemical groups that can allow intrinsic additional functionality. To provide this functionality while maintaining PCL’s positive attributes, blending was performed with a Poly(Ethylene Glycol) (PEG)-based Acrylate endcapped Urethane-based Precursor (AUP). AUPs are a group of polymers, built on a backbone of existing polymers, which introduce additional functionality by the addition of one or more acrylate groups that terminate the polymer chain of a backbone polymer. By blending with a 20kDa AUP-PEG in small amounts, it is shown that MEW attributes are preserved, producing high-quality meshes. Blends were produced in various PCL:AUP weight ratios (100:0, 90:10 and 0:100) and processed into both solvent-cast films and MEW meshes that were used to characterise the properties of the blends. It was found that the addition of AUP-PEG to PCL significantly increases the hydrophilicity of structures produced with these polymers, and adds swelling capability compared to the non-swelling PCL. The developed blend (90:10) is shown to be processable using MEW, and the quality of manufactured scaffolds is evaluated against pure PCL scaffolds by performing scanning electron microscopy image analysis, with the quality of the novel MEW blend scaffolds showing comparable quality to that of pure PCL. The presence of the functionalisable AUP material on the surface of the developed scaffolds is also confirmed using fluorescence labelling of the acrylate groups. Biocompatibility of the MEW-processable blend was confirmed through a cell viability study, which found a high degree of cytocompatibility.

Synthesis of composite films using polymer blends of chitosan and cellulose nanocrystals from marine origin

Thin films reinforced with chitosan and cellulose nanocrystals (CNC) were produced using the casting process. In this study, the impact of plasticisers and sizing agents such as glycerol and polyvinyl alcohol (PVA) respectively on morphological, structural, thermal, and mechanical properties was investigated. The results showed the blends of CNC/PVA/glycerol gave better results when compared to films produced by blends of chitosan/PVA/glycerol films and chitosan/CNC/PVA/glycerol films. The UV spectroscopy showed 65% transmittance for chitosan/PVA/glycerol films, while the film of CNC/PVA/glycerol showed transmittance of 40%. The transmittance of chitosan/CNC/PVA/glycerol showed 75%. The films formed by the combination of CNC/PVA/glycerol showed better stress/strain properties than other films. The films of all combinations showed good thermal stability between the range of 350 and 450 °C. The morphological study using SEM revealed smooth texture for all the films. The study suggests that the films produced may be used for the food packaging applications due to its thermal stability and stress/strain properties.

Flexible Resistive Gas Sensor Based on Molybdenum Disulfide-Modified Polypyrrole for Trace NO2 Detection.

High sensitivity and selectivity and short response and recovery times are important for practical conductive polymer gas sensors. However, poor stability, poor selectivity, and long response times significantly limit the applicability of single-phase conducting polymers, such as polypyrrole (PPy). In this study, PPy/MoS2 composite films were prepared via chemical polymerization and mechanical blending, and flexible thin-film resistive NO2 sensors consisting of copper heating, fluorene polyester insulating, and PPy/MoS2 sensing layers with a silver fork finger electrode were fabricated on a flexible polyimide substrate using a flexible electronic printer. The PPy/MoS2 composite films were characterized using X-ray diffraction, Fourier-transform infrared spectroscopy, and field-emission scanning electron microscopy. A home-built gas sensing test platform was built to determine the resistance changes in the composite thin-film sensor with temperature and gas concentration. The PPy/MoS2 sensor exhibited better sensitivity, selectivity, and stability than a pure PPy sensor. Its response to 50 ppm NO2 was 38% at 150 °C, i.e., 26% higher than that of the pure PPy sensor, and its selectivity and stability were also higher. The greater sensitivity was attributed to p-n heterojunction formation after MoS2 doping and more gas adsorption sites. Thus, PPy/MoS2 composite film sensors have good application prospects.

Development of Blend Polymer Films for Wound Dressing Containing the Chlorhexidine-Loaded Nanoparticles for Controlled Drug Release

Development of Blend Polymer Films for Wound Dressing Containing the Chlorhexidine-Loaded Nanoparticles for Controlled Drug Release

TDAE aromatic oil preference for polymer blends: An analysis of S-SBR, BR, and miscible S-SBR/BR systems

This study assesses the impact of Treated Distillate Aromatic Extract (TDAE) oil, at concentrations of 0–20 parts per hundred rubber (phr), on the glass transition temperature (Tg) of High Vinyl/Low Styrene Styrene-Butadiene Rubber (HVLSS-SBR), polybutadiene rubber (BR), and their blends with weight ratios of 70/30 and 50/50. Using Dynamic Mechanical Analysis, Broadband Dielectric Spectroscopy, and Positron Annihilation Lifetime Spectroscopy, we found that TDAE modifies Tg and fractional free volume (Fv) differently across materials. In HVLSS-SBR, TDAE reduced Tg by approximately 10 °C and increased Fv by 0.8 %. In BR, TDAE raised Tg by 5–7 °C without altering Fv. The 70/30 blend showed no Tg change but a 0.6 % Fv increase. For the 50/50 blend, one Havriliak-Negami equation indicated a Tg rise of 2–3 °C and a 0.4 % Fv increase. A two-equation analysis revealed a 6 °C Tg increase and 0.9 % Fv boost in the BR-rich phase, versus a 2 °C rise and 0.3 % Fv uptick in the HVLSS-SBR-rich phase. The sequence of compatibility, influenced by TDAE, is crystalline BR > amorphous BR > HVLSS-SBR >70/30 blend >50/50 blend. This study provides valuable insights into the behavior of TDAE oil in rubber blends and can serve as a basis for further research in this field.

Improved rapid gas decompression of novel NBR-CTS polymer blends

Nitrile rubber (NBR) and polysulfides are two classes of polymers known for their resistance against swelling when in direct contact with hydrocarbon-based oils and non-polar solvents. In this study nitrile rubber (NBR) and a cyclic tetrasulfide (CTS) are combined with a goal of achieving a rubber blend that has superior properties than of each component. The role of CTS in the blend is discussed, as it presents several functions. This study represents a fundamental analysis of NBR-CTS blends, starting with polymeric phase analysis by Scanning Electron Microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDX). Thermodynamic compatibility studies are deployed in this study to illustrate the materials’ compatibility. Mechanical properties with an emphasis on Payne effect were also studied for blends of NBR-CTS. The synergistic effect found between NBR and CTS can be further expanded in a practical application of rapid gas decompression test as a side-by-side comparison for NBR and NBR-CTS blend compounds. This type of polymer blend represents a potential replacement of fluoroelastomers.

Photoinduced Reversible Disentanglement-Entanglement Transition in partially miscible azobenzene polymer blends

Entanglements, an intrinsic feature of long chains, are critical to the rheological and mechanical properties of polymers. Adding low molecular weight solvents or oligomers into entangled polymers can reduce the entanglements, but the entanglement cannot recover without removing the solvents. Reversible control of the entanglement degree is still a big challenge. In this work, we introduce the azobenzene polymer (Pazo) with reversible photoswitchable side-chain conformation as dynamic diluent into entangled poly(butyl methacrylate) (PBMA) to form a partially miscible blend system. The reduction of entanglement of PBMA by trans-Pazo is similar to a typical solvent, while an unexpectedly stronger tube dilation effect was found for cis-Pazo. Cis-Pazo/PBMA blends exhibit a stronger dependence of plateau modulus on PBMA content, GN(φ)∼φ4.5, which is significantly different from the well-established relation GN(φ)∼φ2 for polymer solutions and blends. The cis-Pazo can disentangle PBMA at a much lower concentration (∼55 %) than the trans-Pazo (>70 %). Pazo content of 55 %–70 % can induce a completely unentangled state of PBMA in Pazo/PBMA blends when Pazo is in the cis state after UV light irradiation, and the entanglement can recover when it is transformed to the trans state. Adding azobenzene polymer does not alter the activation energy of the re-entanglement process.

Studies on ionic conductivity, linear and non-linear optical properties of ecofriendly methyl cellulose: sodium bromide based solid polymer blend electrolytes

Biopolymer electrolytes based on methyl cellulose (MC) and sodium bromide(NaBr) have been prepared through solvent casting technique. Both the concentrations of MC and NaBr are varied. The prepared biopolymer electrolytes have been subjected to AC impedance and UV-Vis spectroscopic techniques. The ionic conductivity reached a maximum value of 4.84 × 10−8 Scm−1 for 0.8 g of MC and 0.2 g of NaBr. UV studies revealed that low direct and indirect band gaps have been observed for the maximum ionic conducting sample. Other optical parameters, such as refractive index, extinction coefficient, skin depth, and optical conductivity, have been estimated. The single-oscillator energy (Eo ) and dispersion energy (Ed ) for all the prepared biopolymer electrolyte samples were calculated with the help of Wemple and DiDomenico single oscillator model. The higher-order non-linear susceptibility values were also calculated. Polymer electrolytes are found to be suitable for optical and electronic devices.

The study on the micromechanical mechanism of PP/EPDM blends and PP/SEBS blends using atomic force microscopy-based nanomechanics

Using atomic force microscope-based nanomechanics to measure the micromechanical properties of different polymer blends, we found that the miscibility of the blend system affects the phase structure and micromechanical properties at the nanoscale, which further affects macroscopic mechanical properties of materials. In the immiscible polypropylene/ethylene propylene diene rubber blends, the microscopic phase structure is connected to the macroscopic mechanical properties of the material, since the microscopic modulus of elasticity of the phases remains constant even if the blend ratio is changed. On the other hand, in the partially miscible polypropylene/styrene-ethylene-butylene-styrene block copolymer blends, the macroscopic mechanical properties of the material are determined by the combination of the microscopic phase structure and the microscopic elastic modulus, because the microscopic elastic modulus of each phase changes with the blending ratio.

Assembly of functional carboxymethyl cellulose/polyethylene oxide/anatase TiO2 nanocomposites and tuning the dielectric relaxation, optical, and photoluminescence performances

Nanocomposite films consisting of carboxymethyl cellulose, polyethylene oxide (CMC/PEO), and anatase titanium dioxide (TO) were produced by the use of sol-gel and solution casting techniques. TiO2 nanocrystals were effectively incorporated into CMC/PEO polymers, as shown by X-ray diffraction (XRD) and attenuated total reflectance fourier transform infrared (ATR-FTIR) analysis. The roughness growth is at high levels of TO nanocrystals (TO NCs), which means increasing active sites and defects in CMC/PEO. In differential scanning calorimetry (DSC) thermograms, the change in glass transition temperature (T g) values verifies that the polymer blend interacts with TO NCs. The increment proportions of TO NCs have a notable impact on the dielectric performances of the nanocomposites, as observed. The electrical properties of the CMC/PEO/TO nanocomposite undergo significant changes. The nanocomposite films exhibit a red alteration in the absorption edge as the concentration of TO NCs increases in the polymer blend. The decline in the energy gap is readily apparent as the weight percentage of TO NCs increases. The photoluminescence (PL) emission spectra indicate that the sites of the luminescence peak maximums show slight variation; peaks get wider, while their intensities decrease dramatically as the concentration of TO increases. These nanocomposite materials show potential for multifunctional applications including optoelectronics, antireflection coatings, photocatalysis, light emitting diodes, and solid polymer electrolytes.