Progress in Carbon Fiber and Its Polypropylene- and Polyethylene-Based Composites

Due to their lightweight and excellent toughness, carbon fiber (CF) and its reinforced thermoplastic composites are suitable for high-performance applications such as aerospace, aviation, automotive and sport equipments. In this study, comprehensive detail is provided on the production of carbon fiber, its various forms and geometry and their corresponding effects on the mechanical properties of CF and its reinforced polypropylene (PP) and polyethylene (PE) composites. Here we discuss extensively various methods reported in literature on improving the interfacial fiber-matrix adhesion and dispersion in order to achieve better mechanical properties for such composites.     

Biobased adhesives,gums, emulsions,and binders: current trends and future prospects

Biopolymers derived from renewable resources are an emerging class of advanced materials that offer many useful properties for a wide range of food and nonfood applications. Current state of the art in research and development of renewable polymers as adhesives, gums, binders, and emulsions is the subject of this review. Much of the focus will be on major biopolymers such as starch, proteins, lignin, oils, and their derivatives found in both natural and modified forms, but other biopolymers of promising commercial interest will also be included where warranted. Polymers produced in nature are remarkably diverse in their chemistry, thermomechanical properties, rheology, plasticity, and chemical reactivity. In particular, their capacity to undergo a wide array of chemical modifications yields materials with tailored properties suitable for use as adhesives, gums, coatings, emulsions, and binders. Many such materials are now widely used in commercial products like building materials, lubricants, sealants, coatings, bonding aids, pharmaceuticals, paper, glues, flocculants, processed and frozen foods, as well as tissue engineering and bone repair products. This review provides a general overview of biobased polymers highlighting their source, availability, properties, and usage in industrial products along with the future prospects, challenges, and opportunities they offer.     

The Anti-Fasciolasis Properties of Silver Nanoparticles Produced by Trichoderma harzianum and Their Improvement of the Anti-Fasciolasis Drug Triclabendazole

Recently, new strains of Fasciola demonstrated drug resistance, which increased the need for new drugs or improvement of the present drugs. Nanotechnology is expected to open some new opportunities to fight and prevent diseases using an atomic scale tailoring of materials. The ability to uncover the structure and function of biosystems at the nanoscale, stimulates research leading to improvement in biology, biotechnology, medicine and healthcare. The size of nanomaterials is similar to that of most biological molecules and structures; therefore, nanomaterials can be useful for both in vivo and in vitro biomedical research and applications. Therefore, this work aimed to isolate fungal strains from Taif soil samples, which have the ability to synthesize silver nanoparticles. The fungus Trichoderma harzianum, when challenged with silver nitrate solution, accumulated silver nanoparticles (AgNBs) on the surface of its cell wall in 72 h. These nanoparticles, dislodged by ultrasonication, showed an absorption peak at 420 nm in a UV-visible spectrum, corresponding to the plasmon resonance of silver nanoparticles. The transmission electron micrographs of dislodged nanoparticles in aqueous solution showed the production of reasonably monodisperse silver nanoparticles (average particle size: 4.66 nm) by the fungus. The percentage of non hatching eggs treated with the Triclabendazole drug was 69.67%, while this percentage increased to 89.67% in combination with drug and AgNPs.     

Polymerization behavior of methylol-functional benzoxazine monomer

This study focuses on methylol functional benzoxazines as precursors to build a network structure utilizing both benzoxazine and resole chemistry. The first part is a review of systems that contain methylol groups which play a role on their crosslinking formation. The polymerization mechanism and properties of resoles will be highlighted as the most abundant polymers that are characterized by polymerization through condensation reaction of methylol group. In the second part, the effect of incorporating methylol group into benzoxazine monomers is studied. Differential scanning calorimetry (DSC) is used to study the effect of methylol group on the rate of polymerization. Kissinger and Ozawa methods using non-isothermal DSC at different heating rates show that methylol monomer exhibits lower average activation energy compared to the un-functionalized monomer. The effect of adding catalysts into the monomers is also studied. p-Toluene sulfonic acid (PTSA) is found to be more efficient than 1-methyl-imidazole (IMD) and lithium iodide (LiI) in the case of methylol monomer due to its ability of accelerating both the methylol condensation and ring-opening polymerization. Additionally, thermal behavior of the monomers is studied using thermogravimetric analysis (TGA).     

Impact of hydrogen concentrations on the impedance spectroscopic behavior of Pd-sensitized ZnO nanorods

ZnO nanorods were synthesized using a low-cost sol-gel spin coating technique. The synthesized nanorods were consisted of hexagonal phase having c-axis orientation. SEM images reflected perpendicular ZnO nanorods forming bridging network in some areas. The impact of different hydrogen concentrations on the Pd-sensitized ZnO nanorods was investigated using an impedance spectroscopy (IS). The grain boundary resistance (R_gb) significantly contributed to the sensing properties of hydrogen gas. The boundary resistance was decreased from 11.95 to 3.765 kΩ when the hydrogen concentration was increased from 40 to 360 ppm. IS gain curve showed a gain of 6.5 for 360 ppm of hydrogen at room temperature. Nyquist plot showed reduction in real part of impedance at low frequencies on exposure to different concentrations of hydrogen. Circuit equivalency was investigated by placing capacitors and resistors to identify the conduction mechanism according to complex impedance Nyquist plot. Variations in nanorod resistance and capacitance in response to the introduction of various concentrations of hydrogen gas were obtained from the alternating current impedance spectra.     

Mild hydrocracking of 1-methyl naphthalene (1-MN) over alumina modified zeolite

The catalytic activity and life of the NiMoS supported on alumina–USY zeolite (physical mixture of alumina and USY (NMAZ), USY zeolite coated with alumina (NMACZ-2)) were compared in the hydrocracking of 1-methyl naphthalene by a single run at the several reaction temperatures between 360 and 400 °C as well as repeated runs at 360 °C. The relative activity of NMAZ is slightly higher after 1 h at all reaction temperatures, but was lower after 2 h at reaction temperatures above 380 °C. The preference of NMACZ-2 became distinct and definite by further increasing the reaction time at all reaction temperatures. Too long reaction time, particularly at higher reaction temperature, decreased the yield of (alkyl)benzenes, indicating the significant progress of the successive reactions. Thus, the highest yield of alkyl(benzenes) of about 97% was obtained over NMACZ-2 after 4 h at 380–390 °C. This was much less than the yield of about 82% obtained over NMAZ after 4 h at 370 °C. Ten repeated runs at 360 °C for 6 h resulted in marked decrease of yield over NMAZ from 73% to 64%, while the decrease in yield over NMACZ-2 was only from about 80% to 78%. The decrease of catalytic activity appears to reflect the coke formation on the USY which occurs on the naked acidic site of the substrate, which are rather isolated from the NiMoS on alumina. In contrast, alumina-coated support keeps USY underneath the alumina, which carries NiMoS and acidic sites on the same surface. The acidity of surface alumina is moderated by the underneath USY. The adequate acidity of the neighboring NiMoS and high hydrogenation activity provide a good balance resulting in an excellent catalytic activity and life of NiMoS supported on alumina-coated USY zeolite.     

Removal of toxic aqueous ions using amorphous AlPO4

Aluminium phosphate (AlPO₄) was characterized using X-ray diffractometry (XRD), Fourier Transform infrared (FTIR), point of zero charge (PZC) and dissolution studies. XRD showed the sample to be amorphous, FTIR confirmed the presence of OH groups on the surface and PZC was determined at pH 3.45. The dissolution study illustrated a decrease in dissolution with an increase in the pH. Potentiometric titration data were fit to the Gaines–Thomas equation, which showed that AlPO₄ is a weakly acidic ion exchanger. Sorption studies were carried out at pH 4–6 and temperatures 293–323 K. The uptake of metal ions was observed to increase with an increase in the pH and temperature. The surface selectivity towards metal ions was found in the order Pb²⁺> Cu²⁺> Cd²⁺. Sorption data were fit to the new equation derived from the proposed mechanism for metal ion uptake. Various parameters such as stoichiometry of the surface H⁺ ion release, equilibrium constant, standard enthalpy, entropy and free energy changes were evaluated from the plots. The values of all these parameters were found to be closely related to the values reported in the literature.     

Corrosion protection of commercial steel using stainless steel coatings deposited by Cathodic Arc Plasma Deposition technique

The commercial steel AISI 1010 was coated with AISI 316L steel using Cathodic Arc Plasma Deposition (CAPD) technique. The coatings were deposited in vacuum and in the presence of nitrogen, acetylene and mixture of the two as reactive gases. The coatings were deposited as a function of time while other parameters remained constant. The coatings 0.75 to 1.3 μm thick were adherent and amorphous. The aqueous corrosion properties of the coated samples in 3.5 wt % NaCl solution were studied by Tafel, cyclic and potentiodynamic polarization measurements. The derived corrosion parameters were then compared among the various uncoated and coated samples. The study revealed that the coated samples were more corrosion resistant than the uncoated one. Similarly, the samples coated in the nitrogen + acetylene mixture atmosphere were more corrosion resistant than the samples coated in only nitrogen and acetylene atmospheres. The corrosion parameters were also compared as a function of coating time to ascertain best coating thickness.     

Biodegradable composites based on starch/EVOH/glycerol blends and coconut fibers

Unripe coconut fibers were used as fillers in a biodegradable polymer matrix of starch/ethylene vinyl alcohol (EVOH)/glycerol. The effects of fiber content on the mechanical, thermal, and structural properties were evaluated. The addition of coconut fiber into starch/EVOH/glycerol blends reduced the ductile behavior of the matrix by making the composites more brittle. At low fiber content, blends were more flexible, with higher tensile strength than at higher fiber levels. The temperature at the maximum degradation rate slightly shifted to lower values as fiber content increased. Comparing blends with and without fibers, there was no drastic change in melt temperature of the matrix with increase of fiber content, indicating that fibers did not lead to significant changes in crystalline structure. The micrographs of the tensile fractured specimens showed a large number of holes resulting from fiber pull‐out from the matrix, indicating poor adhesion between fiber and matrix. Although starch alone degraded readily, starch/EVOH/glycerol blends exhibited much slower degradation in compost. Composites produced 24.4–28.8% less CO₂ compared with starch in a closed‐circuit respirometer. Addition of increasing amount of fiber in starch/EVOH/glycerol composite had no impact on its biodegradation. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009