All‐polymer electromechanical systems consisting of electrostrictive poly(vinylidene fluoride‐trifluoroethylene) and conductive polyaniline

The low elastic modulus and the ability to withstand high strain without failure make the conducting polymer attractive for a wide range of acoustic applications based on high‐strain electroactive polymers. In this article, we examine the electric and electromechanical performance of all‐polymer electromechanical systems, fabricated by painting conductive polyaniline (PANI) doped with camphor sulfonic acid (HCSA) on both sides of electrostrictive Poly(vinylidene fluoride‐trifluoroethylene) (P(VDF‐TrFE)) copolymer films, and compare them with those from the same copolymers with gold electrodes. The all‐polymer composite films are flexible, with strong coherent interfaces between the electrostrictive polymer layer and the conductive polymer layer. The electric performance such as dielectric properties and polarization hysteresis loops from P(VDF‐TrFE)/PANI film is nearly identical to those of P(VDF‐TrFE)/gold films in a wide temperature (from −50 to 120°C), and frequency range (from 1 Hz to 1 MHz). The all‐polymer systems also show a similar or even larger electric field induced strain response than that of films with electrodes under identical measurement conditions. The results demonstrate that the polyaniline/HCSA is good candidate material as the electrodes for electroactive polymers. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 945–951, 2000     

Effect of phosphorus on activity of hydrotreating catalyst of Maya heavy crude

The effect of phosphorus on physical properties of the catalyst and on activity of hydrotreating of Maya crude was studied in this work. Catalysts were prepared by the co-impregnation method. Alumina-titania binary oxide was used as a support material. The presence of phosphorus in the catalyst decreases the percentage of micropores, and it results in a decrease of specific surface area. Temperature program reduction (TPR) shows that phosphates reduce metal support interaction. It leads to the formation of polymolybdate phases in expense of strongly bonded tetrahedral molybdates. At higher P loading, polymolybdates may be present with quasi crystalline MoO₃. However, the TPR experiment is not sufficiently sensitive to distinguish several phases present on the catalysts used by the authors. A slight increment of HDM activity is observed, but HDS activity is lower in the P containing catalyst compared with the P free catalyst. The changes of physical properties of the spent catalysts are mainly due to the coke formation on the catalyst. The presence of phosphorus on hydrotreating catalysts inhibits coke formation during the hydrotreating reaction.     

Maya crude hydrodemetallization and hydrodesulfurization catalysts: An effect of TiO2 incorporation in Al2O3

Hydrotreating of Maya heavy crude oil over high specific surface area CoMo/TiO₂–Al₂O₃ oxide supported catalysts was studied in an integral reactor close to industrial practice. Activity studies were carried out with Maya crude hydrodesulfurization (HDS), hydrodemetallization (HDM), hydrodenitrogenation (HDN), and hydrodeasphaltenization (HDAs) reactions. The effect of support composition, the method of TiO₂ incorporation, and the catalyst deactivation are examined. Supported catalysts are characterized by BET specific surface area (SSA), pore volume (PV), pore size distribution (PSD), and atomic absorption. It has been found that sulfided catalysts showed a wide range of activity variation with TiO₂ incorporation into the alumina, which confirmed that molybdenum sulfided active phases strongly depend on the nature of support. The pore diameter and nature of the active site for HDS, HDM, HDN, and HDAs account for the influence of the large reactant molecules restricted diffusion into the pore, and/or the decrease in the number of active sites due to the MoS₂ phases buried with time-on-stream. The textural properties and hysteresis loop area of supported and spent catalysts indicated that catalysts were deactivated at the pore mouth due to the metal and carbon depositions. The atomic absorption results agreed well regarding the textural properties of spent catalysts. Thus, incorporation of TiO₂ with γ-Al₂O₃ alters the nature of active metal interaction with support, which may facilitate the dispersion of active phases on the support surface. Therefore, the TiO₂ counterpart plays a promoting role to HDS activity due to the favorable morphology of MoS₂ phases and metal support interaction.     

The anti-microbial activity of titania-nickel ferrite composite nanoparticles

A novel approach to synthesize a new generation of composite nanoparticles consisting of a photocatalytic shell of anatase-titania and a magnetic core of nickel ferrite has been adopted combining reverse micelle and chemical hydrolysis techniques. Titania is an effective anti-microbial agent that can be directly sprayed on infected areas of the human body or environment. Unfortunately, titania is an electrical insulator and is difficult to extract from the sprayed surface after treatment. The titania photocatalytic shell provides good antimicrobial capability that renders the bacteria inactive and removes the organic pollutants, while the nickel ferrite magnetic core enables controlled delivery of composite nanoparticles through the application of a small magnetic field, encouraging their application as removable anti-microbial photocatalyst nanoparticles. For more information, contact R.D.K. Misra, University of Louisiana at Lafayette, Center for Structural and Functional Materials, P.O. Box 44130, Lafayette, LA 70504-4130; (337) 482-6430; e-mail dmisra@louisiana.edu.     

Synergetic effects of organic and inorganic additives on improvement in hydrophilicity and performance of PVDF antifouling ultrafiltration membrane for removal of natural organic material from water

Surrounding vegetation, animal, human and microbiological decomposition are the strong source of humic acid (HA) falling into the surface water bodies through rain runoff in the monsoon. HA contains various functional groups, such as carboxylic, phenolic, hydroxyl, and quinine, which are the major foulant. Contact of HA may have an adversarial health issue to human beings namely goiter, black foot, and cancer disease. The maximum permissible limit of HA in drinking water should be less than 2 ppm as per the Environmental Protection Agency (EPA). The membrane technology has prevailed a prominent place worldwide in chemical, water and wastewater treatment technologies. The proposed work is focused on the blending of organic-water soluble polymer polyethylene glycol 6000 as a pore-forming agent and inorganic salt lithium bromide (LiBr) as membrane morphology modifier with polyvinylidene fluoride host polymer in the N,N-Dimethylacetamide solvent. All fabricated membranes were characterized for functional groups and morphology. The total number of pores per unit surface area of membrane for membranes M-LiBr-0, M-LiBr-1, M-LiBr-2, and M-LiBr-3 are 2 × 10¹³, 2.3 × 10¹⁴, 2.7 × 10¹⁴ and 2.82 × 10¹⁴, respectively. The static water contact angle was decreased from 68.2° to 50.6° with an increase in the content of LiBr from 0 to 3 wt%. The order of pure water flux and hydraulic permeability of the membrane was M-LiBr-0 < M-LiBr-1 < M-LiBr-2 < M-LiBr-3. The HA rejection of the membrane was also increased from 90.13% to 96.24% with LiBr content due to a decrease in pore size of the membrane with the addition of LiBr content.     

A bio-inspired gelatin-based pH- and thermal-sensitive magnetic hydrogel for in vitro chemo/hyperthermia treatment of breast cancer cells

Gelatin (Gel)-based pH- and thermal-responsive magnetic hydrogels (MH-1 and MH-2) were designed and developed as novel drug delivery systems (DDSs) for cancer chemo/hyperthermia therapy. For this goal, Gel was functionalized with methacrylic anhydride (GelMA), and then copolymerized with (2-dimethylaminoethyl) methacrylate (DMAEMA) monomer in the presence of methacrylate-end capped magnetic nanoparticles (MNPs) as well as triethylene glycol dimethacrylate (TEGDMA; as crosslinker). Afterward, a thiol-end capped poly(N-isopropylacrylamide) (PNIPAAm-SH) was synthesized through an atom transfer radical polymerization technique, and then attached onto the hydrogel through “thiol-ene” click grafting. The preliminary performances of developed MHs for chemo/hyperthermia therapy of human breast cancer was investigated through the loading of doxorubicin hydrochloride (Dox) as an anticancer agent followed by cytotoxicity measurement of drug-loaded DDSs using MTT assay by both chemo- and chemo/hyperthermia-therapies. Owing to porous morphologies of the fabricated magnetic hydrogels according to scanning electron microscopy images and strong physicochemical interactions (e.g., hydrogen bonding) the drug loading capacities of the MH-1 and MH-2 were obtained as 72 ± 1.4 and 77 ± 1.8, respectively. The DDSs exhibited acceptable pH- and thermal-triggered drug release behaviors. The MTT assay results revealed that the combination of hyperthermia therapy and chemotherapy has synergic effect on the anticancer activities of the developed DDSs.     

The effect of modifying an edge-plane pyrolytic graphite electrode with single-wall carbon nanotubes on its use for sensing diclofenac

A simple and highly sensitive sensor based on edge-plane pyrolytic graphite electrode (EPPGE) coated with single-wall carbon nanotubes is proposed for diclofenac determination in nanomolar concentrations. The oxidation of diclofenac occurred in two well-defined peaks having peak potentials ∼439 and ∼854 mV at pH 7.2. The modified electrode showed excellent catalytic activity presenting much higher peak currents than those measured on a bare EPPGE. Under the optimum conditions, the calibration curve was linear in the concentration range 1 × 10⁻⁹-500 × 10⁻⁹ M and 25 × 10⁻⁹-1500 × 10⁻⁹ M for peaks I and II, respectively. The limit of detection for peaks I and II was found as 0.82 × 10⁻⁹ and 22.5 × 10⁻⁹ M, respectively. The developed sensor was applied for the determination of diclofenac in biological and pharmaceutical samples using square-wave voltammetry and the validation of results using high performance liquid chromatography showed excellent agreement.     

Design of an Ultra-Compact and Highly-Sensitive Temperature Sensor Using Photonic Crystal Based Single Micro-Ring Resonator and Cascaded Micro-Ring Resonator

Silicon - In the present report, a photonic crystal based micro-ring resonator (MRR) structure is proposed which is very compact in size and has very fast response and is employed for temperature...     

Short jute fiber‐reinforced polypropylene composites: Dynamic mechanical study

Short jute fiber‐reinforced polypropylene (PP) composites were prepared using a high‐speed thermokinetic mixer. A compatibilizer was used to improve the molecular interaction between jute and PP. Both the percent weight fraction of the jute fiber and compatibilizer were varied to study the dynamic mechanical thermal (DMT) properties. Dynamic parameters such as storage flexural modulus (E′), loss flexural modulus (E″), storage shear modulus (G′), loss shear modulus (G″), and loss factor or damping efficiency (tan δ) were determined in a resonant frequency mode. The transition peak nature, amplitude, and temperature of E′, E″, G′, G″, and tan δ of different compositions were shown to indicate possible improvements of molecular interaction in the presence of a compatibilizer. The modulus retention term, a plot of the reduced modulus with the weight fraction of the jute fiber, also indicate its improvement. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 531–539, 1999