An in-Depth Analysis of the Swelling,Mechanical, Electrical,and Drug Release Properties of Agar–Gelatin Co-Hydrogels

Agar–gelatin-based co-hydrogels were prepared with different compositions of the agar and the gelatin fractions. The intermolecular hydrogen bonding was higher in the co-hydrogels as compared to the gelatin hydrogel. Swelling studies indicated diffusion-mediated swelling. The electrical stability of the co-hydrogels was higher as compared to the gelatin hydrogel. Though the firmness of the co-hydrogels was higher, Weichert model of viscoelasticity indicated that the inherent mechanical stability of the gelatin hydrogel was superior. The release of ciprofloxacin hydrochloride was predominately Fickian diffusion-mediated. In gist, the co-hydrogels can be tried as polymeric constructs for controlled drug delivery applications.     

An Insight on the Swelling,Viscoelastic, Electrical,and Drug Release Properties of Gelatin–Carboxymethyl Chitosan Hydrogels

The present study reports the in-depth analysis of the gelatin–carboxymethyl chitosan hydrogels. The composite system formed phase-separated hydrogels, which is confirmed by scanning electron microscopy. The swelling of the carboxymethyl chitosan-containing hydrogels was lower than the gelatin hydrogel. Macroscale deformation study using a static mechanical tester indicated a viscoelastic nature of the hydrogels. A decrease in the impedance of the hydrogels was observed with an increase in the carboxymethyl chitosan content. The drug release from the hydrogels was predominantly Fickian diffusion mediated and was released in its active form. The results suggested the potential use of the hydrogels as drug delivery matrices.     

Preparation,Mechanical and Electrical Properties of Glass and Jute–Epoxy/Epoxy Polyurethane Composites

Glass and jute (treated and untreated) composites of epoxy resin of 1,1′-bis(3-methyl-4-hydroxy phenyl)cyclohexane(EMC) cured using 20% triethylamine as a hardener (G-EMCT-20 and J-EMCT-20) and EMC- polyurethane of toluene diisocyanate (J-EMCPU and TJ-EMCPU) have been prepared by a hand layup technique under 27.58 MPa pressure and at 150°C for 4 h. G-EMCT-20, J-EMCT-20, J-EMCPU and TJ-EMCPU showed 275, 96.5, 37.3 and 31.5 MPa tensile strength; 351, 84, 10 and 24 MPa flexural strength; 5837, 2758, 1277 and 1619 MPa elastic modulus; 24.6, 7.1, 1.9 and 1.6 kV/mm electric strength; and 1.4 × 10¹³, 1.1 × 10¹¹, 7.7 × 10¹⁰ and 3.6 × 10¹⁰ ohm cm volume resistivity, respectively. Fairly good to excellent mechanical and electrical properties of the composites indicated their industrial applications in building and construction, electrical and electronic industries.     

Graft Copolymerization onto Starch–I. Synthesis and Optimization of Starch Grafted with N-tert-Butylacrylamide Copolymer and its Hydrogels

Grafting of N-tert-butylacrylamide (BAM) onto starch in aqueous medium initiated by ceric ammonium nitrate ion has been studied under N₂ atmosphere. The optimum conditions with respect to monomer concentration, initiator concentration, polymerization temperature, polymerization time and material to liquor ratio were studied in terms of percent of grafting efficiency (%GE) and percent of grafting yield (%GY). The optimum conditions obtained for the grafting of BAM on 1.0 g starch were: [BAM]=0.020 mol/L, [CAN]=0.91×10^–3 mol/L, Temperature=30C, and Time=240 min. Starch-g-BAM copolymer was characterized by FTIR, TGA for thermal stability, X-ray diffraction (XRD) for the crystallinity and scanning electron microscope (SEM) for surface morphology of the copolymer. Acid hydrolysis and viscosity average molecular weight (M _v) of copolymer were evaluated for the copolymer. Hydrogels prepared by grafting of BAM onto gelatinized starch showed maximum water uptake and moisture retain of 162% and 63% respectively.     

Physical and Mechanical Properties of Hot-Pressed Materials of the ZrB2–TaC–SiC System

Refractories and Industrial Ceramics - High-density (with a relative density of up to 98.8%) ultra-high-temperature ceramic materials (UHTCs) based on the ZrB2–TaC–SiC system were...     

Evaluation of Physicochemical and Antifungal Properties of Polylactic Acid–Thermoplastic Starch–Chitosan Biocomposites

Biocomposites of polylactic acid, thermoplastic starch, chitosan powder, and chitosan lyophilized powder were prepared using an extrusion process. The color, thermal, structural, mechanical, morphology, and antimicrobial properties were evaluated. The addition of thermoplastic starch and chitosan (chitosan powder and chitosan lyophilized powder) produced significant changes in color and heterogeneous surface morphology of the polylactic acid biocomposites. The thermal, mechanical, and morphometric properties of the material showed changes with the addition of thermoplastic starch and chitosan (chitosan powder and chitosan lyophilized powder). The biocomposites formulated with chitosan powder and chitosan lyophilized powder showed antifungal activity when evaluating this property. The biocomposites produced could be used in packaging applications.     

Preparation,Characterization and Assessment of the Novel Gelatin–tamarind Gum/Carboxymethyl Tamarind Gum-Based Phase-Separated Films for Skin Tissue Engineering Applications

The current study delineates the development of novel gelatin–tamarind gum/carboxymethyl tamarind gum-based phase-separated films for probable skin tissue engineering applications. Polyethylene glycol was used as plasticizer. The films were characterized thoroughly using mechanical tester and impedance analyzer. Cell proliferation ability and drug release properties of the films were investigated. Mechanical studies indicated composition-dependent stress relaxation properties. Polysaccharide containing films supported better proliferation of human keratinocytes as compared to control. Drug-loaded films showed good antimicrobial properties against Escherichia coli. Analysis of the results indicated that the prepared films may be tried as matrices for skin tissue engineering.     

Detonation Properties and Electrical Conductivity of Explosive–Metal Additive Mixtures

Detonation properties of mixtures of condensed high explosives with metal additives are studied. A scheme of measurement of high electrical conductivity of detonation products ( > 10 ^–1 · cm^–1) with a time resolution of 10 nsec is developed. It is shown that the properties of detonation products depend significantly on the content of the additive in the HE and on dispersion and density of the mixture. The electrical conductivity of detonation products of the compositions examined reaches 5 · 10^{3 –1} · cm^–1, which is more than three orders higher than the electrical conductivity of the HE without the additive. Significant variation of electrical conductivity of detonation products over the conducting region thickness has been found. The main conductivity corresponds to a sector 1 mm long near the detonation front. The overdriven state of the detonation wave has a strong effect on electrical conductivity and conducting region thickness. It is assumed that the behavior of electrical conductivity with time is caused by successive processes of shock compression of the HE, excitation of the chemical reaction (including the reaction of the additive with detonation products), and expansion of detonation products. The measurement technique used is highly informative due to the possibility of studying detonation in various regimes.     

Crystallization Behavior,Mechanical Properties,and Chemical Resistance of Leucite–Fluoroapatite Glass-Ceramic Glazes

The roles of Li₂O and B₂O₃ and heat-treatment condition on crystallization behavior and flowability of leucite–fluoroapatite-based glass-ceramic glazes were investigated. The thermal expansion coefficient, mechanical, and chemical properties of the optimum specimen were determined. Glaze firing was performed in the 650–1100°C interval, in one and two step processes. Based on the results, B₂O₃ was more effective than Li₂O in point of flowability view. Also, the microstructures varied with the adopted firing process, so that the two-step heat-treated sample showed superior mechanical properties than the one-step heat-treated specimens.     

Development of Siloxane Based Tetraglycidyl Epoxy Nanocomposites for High Performance Applications—Study of the Thermo Mechanical,Electrical, XRD,EDS and Physical Properties

Silicon - A study was made in the present investigation on siloxane containing tetraglycidyl epoxy nanocomposites to find its suitability for use in high performance applications. The synthesis and...     

Reaction Synthesis and Mechanical Properties of TiB2–AlN–SiC Composites

TiB₂–AlN–SiC (TAS) ternary composites were prepared by reactive hot pressing at 2000°C for 60 min in an Ar atmosphere using TiH₂, Si, Al, B₄C, BN and C as raw powders. The phase composition was determined to be TiB₂, AlN and β-SiC by XRD. The distribution of elements Al and Si were not homogeneous, which shows that to obtain a homogeneous solid solution of AlN and SiC in the composites by the proposed reaction temperatures higher than 2000°C or time duration longer than 60 min are needed. The higher fracture toughness (6·35±0·74 MPa·m^1/2 and 6·49±0·73 MPa·m^1/2) was obtained in samples with equal molar contents of AlN and SiC (TAS-2 and TAS-5) in the TAS composites. The highest fracture strength (470±16 MPa) was obtained in TAS-3 sample, in which the volume ratio of TiB₂/(AlN+SiC) was the nearest to 1 and there was finer co-continuous microstructure. ©     

Dielectric,Mechanical, and Thermal Properties of Low-Permittivity Polymer–Ceramic Composites for Microelectronic Applications

A new low-permittivity polymer–ceramic composite for packaging applications has been developed. The ceramic-reinforced polyethylene and polystyrene composites were prepared by melt mixing and hot molding techniques. Low-loss, low-permittivity Li₂MgSiO₄ (LMS) ceramics prepared by the solid-state ceramic route were used as the filler to improve the dielectric properties of the composites. The relative permittivity and dielectric loss were increased with the increase in the ceramic loading at radio and microwave frequencies. The mechanical properties and thermal conductivity of the Li₂MgSiO₄-reinforced polymer–ceramic composite were also investigated. The stability of the relative permittivity of polymer–ceramic composites with temperature and frequency was investigated. The experimentally observed relative permittivity, thermal expansion, and thermal conductivity were compared with theoretical models.     

Cure Characteristics and Mechanical Properties of Natural Rubber–Layered Clay Nanocomposites

The effect of interlayer distance of nanoclay on mechanical properties, cure characteristics, and swelling resistance of natural rubber (NR) in varying clay proportion were studied. X-ray diffraction results of nanocomposite with 10 phr of nanoclay showed the formation of an intercalated structure. The rate of vulcanization and maximum torque value of the nanocomposite are higher than the gum compound. Nanocomposites with clay having higher interlayer distance shows superior mechanical properties. Mechanical properties gradually increase with increase in clay loading up to 10 phr. A 50% increase in tensile strength and about 150% increase in modulus at 300% elongation were observed for the nanocomposite with 10 phr clay loading. Better barrier properties offered by the nanocomposites due to the presence of tortous path was confirmed by the Nielson's model.     

Synthesis,Structure, Photoluminescent and Drug Loading and Release Properties of a Novel Cadmium (II) Coordination Polymers Based on Terphenyl–3, 4″, 5–tricarboxylic Acid

A stable three-dimensional coordination complex, {[Cd_1.5(tta)(H₂O)_4.5]·H₂O}_n (1) (tta?=?terphenyl—3,4″,5—tricarboxylic acid), was prepared by the solvothermal reaction of Cd(CH₃COO)₂·2H₂O and tta in water, which was characterized by infrared spectroscopy, single-crystal X-ray diffraction, powder X-ray diffraction, fluorescence, and thermogravimetric analyses. In the solid state of this compound, the Cd (II) center displayed a distorted trigonal bipyramid coordination sphere consisting of two oxygen atoms from two different carboxyl which were offered by two separate tta ligands and three oxygen atoms from three water molecules. The one-dimensional linear (1D) structure and two-dimensional plane were formed by Cd-O coordination bond while the 3D supramolecular reticular structure was formed by hydrogen-bond interactions. And there are large rectangular holes whose size are 13.30?×?13.31 Å along crystallographic axis a. The drug loading content (DLC) of 1 was 0.203 g (Ibu)/g (compound) and the release was desirable.     

Construction and Properties of Double-Crosslinked Hydrogels Based on Host–Guest Interactions/UV Polymerization

Supramolecular hydrogels based on host–guest interactions have inherent flaw that the host molecules easily slide on or fall off the linear guest molecules, causing collapse of the networks. Hence, a double-crosslinking strategy is introduced in this study. The primary crosslinking formed via host–guest interactions between α-cyclodextrin (α-CD) and poly(ethylene glycol) dimethacrylate (PEGDMA) or between α-CD and four-arm poly(ethylene glycol) methacrylate (4arm PEG-MA). Then, secondary networks among PEGDMA or 4arm PEG-MA formed via UV-induced crosslinking. Results show that the fracture stress and fracture strain of PEGDMA-α-CD double-crosslinked hydrogels (P-C-U) increases up to 0.63 MPa and 71%, respectively, which significantly affected by molecular weight of PEGDMA. The double-crosslinking strategy helps increase the toughness up to 12.9 MJ m⁻³ (P_6k-0.025M-C-U) and 17.23 MJ m⁻³ (4P_10k-0.025M-C-U), as well as impart a certain degree of fatigue resistance to both PEGDMA hydrogels and 4arm-PEG-MA hydrogels, which is believed to be due to the energy dissipation mechanism introduced in the structure. The swelling capacity of double-crosslinked hydrogels is decreased compared to that with single-UV-crosslinked hydrogels, may be because the double-crosslinking strategy increases the crosslinking density of the hydrogel structure. In addition, both the molecular weight and concentration of PEGDMA and 4arm-PEG-MA influences the swelling capacity of the double-crosslinked hydrogels.     

Evaluation of the Effect of Nanosilica on Thermal and Mechanical Properties of Metal–Metal and Metal–Glass Canola-Based Polyurethane/Nanosilica Adhesives

Nanocomposites with different concentration of nanofiller were prepared by adding nanosilica to the canola-based polyurethane matrix via in situ polymerization. The effect of nanosilica on the mechanical properties of adhesives was evaluated by tensile tests. Adhesive characteristics on metal–metal and metal–glass bondings were also evaluated by lap shear strength tests. Incorporation of nanosilica into the canola-based polyurethane enhanced both tensile and lap shear strength of synthesized adhesives. Also the effect of nanoparticles on glass transition temperature and thermal stability was investigated by differential scanning calorimetry and thermogravimetric analysis, respectively. The increase of nanosilica content in the polyurethane adhesives, thermal property of the nanocomposites improved.     

Study on Synthesis and Chloramphenicol Release of Poly（2-hydroxyethylmethacrylate-co-acrylamide） Hydrogels

In this article, poly（2-hydroxyethylmethacrylate-co-acrylamide） hydrogels were synthesized by bulk free-radical copolymerization of 2-hydroxyethylmethacrylate （HEMA） and acrylamide （AAm） for soft contact lens（SCL）-based ophthalmic drug delivery system. The copolymer was characterized with FT-IR and SEM, the swelling property of the hydrogels were studied by gravimetrical method, and chloramphenicol was used as a model drug to investigate drug release profile of the hydrogels. The results showed that poly（2-hydroxyethylmethacrylateco-acrylamide） hydrogels were transparent and useful SCL biomaterial, the water content increased as AAm content increase and pH decrease, and in the same way, hydrogel composition affected chloramphenicol release process too. Migration rate of chloramphenicol increased as the AAm content in the hydrogels increased in the first stage of diffusion process, whereas there was no significant difference thereafter.     

In situ–Directed Growth of Organic Nanofibers and Nanoflakes: Electrical and Morphological Properties

Organic nanostructures made from organic molecules such as para-hexaphenylene (p-6P) could form nanoscale components in future electronic and optoelectronic devices. However, the integration of such fragile nanostructures with the necessary interface circuitry such as metal electrodes for electrical connection continues to be a significant hindrance toward their large-scale implementation. Here, we demonstrate in situ–directed growth of such organic nanostructures between pre-fabricated contacts, which are source–drain gold electrodes on a transistor platform (bottom-gate) on silicon dioxide patterned by a combination of optical lithography and electron beam lithography. The dimensions of the gold electrodes strongly influence the morphology of the resulting structures leading to notably different electrical properties. The ability to control such nanofiber or nanoflake growth opens the possibility for large-scale optoelectronic device fabrication.     

Effect of Direct Dyes on the Physical and Mechanical Properties of α-Keratin Fibers

Fibre Chemistry - The effect of direct dyes on the physical and mechanical properties of human hair (a-keratin fibers) in the native state and subjected to bleaching with Estel haute couture...     

In situ Reaction Synthesis and Mechanical Properties of TaC–TaSi2 Composites

TaC–TaSi₂ composites were fabricated at 1700°C by an in situ reaction/hot pressing method using Ta, Si, and graphite as initial materials. TaSi₂ content was 0–100 vol%. The microstructure and mechanical properties of the composites were investigated. It was found that the relative densities of composites were above 97.5% when the volume content of TaSi₂ was above 10%. The TaC/10 vol% TaSi₂ composite presented the highest flexural strength of 376 MPa. When the TaSi₂ content was 30–50 vol%, the composites showed the highest fracture toughness of about 4.3 MP·am^1/2. In addition, the composites could retain high Young's modulus up to at least 1525°C.