Highly transparent antibacterial hydrogel-polymeric contact lenses doped with silver nanoparticles

Biocompatible polymers such as poly(vinyl alcohol) (PVA) and poly(vinyl pyrrolidone) are used to prepare hydrogels for biomedical applications, including optical applications such as the manufacture of sensing devices, cosmetic and smart, and medical contact lenses, among others. In this study, three contact lenses were prepared by doping PVP-PVA supportive hydrogel with 0.1, 0.5, and 1 wt% of laboratory-manufactured Ag NPs. The work demonstrates the evaluation of vision correction through each lens and the effect of changing the concentration of silver on its refractive index. The simulation involved the design and simulation of an aberrated human eye based on the Liou and Brennan model (LBM), and the insertion of the contact lenses for vision correction using the ZEMAX optical design program. This work also included a study of the antimicrobial properties of the resulting hydrogel contact lenses doped with Ag NPs. The resulting refractive index of one PVP-PVA-Ag lens was relatively high at 532 nm = 1.604, which made the lens provide the highest image contrast (the lowest MTF curve degradation) of 0.883 ± 0.027 at 20 cycles/mm and an RMS nearly the Airy disc diameter of 3.983 μm. PVA was used in combination with PVP for stabilizing Ag NPs to give the contact lenses an antibacterial property. Finally, the optimum contact lens with a 1 wt% Ag NPs concentration showed the highest inhibition activity.     

Effect of partial delignification of kenaf bast fibers for radiation graft copolymerization

Malaysian kenaf bast fiber was treated by acidic chlorite to be applied for a trunk polymer radiation‐induced graft copolymerization. The delignification conditions such as temperature, reaction time, and sodium chlorite (NaClO₂) loading were optimized from the viewpoints of density, tensile strength, and reactivity of grafting. It was found that delignification condition at 80°C for 6 h with 0.5% NaClO₂ gave 91% of lignin removal from the kenaf bast fibers. In this case, the density, fineness, and tensile strength of the kenaf fiber decreased about 46, 44, and 87%, respectively. Reactivity of grafting was evaluated using 4‐chloromethyl styrene to obtain widely available precursor materials. The partial delignified kenaf with residual lignin less than 2% resulted in degree of grafting of 134%, which is enough for precursor materials. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

PARAMETER ESTIMATION OF FICK'S LAW DRYING EQUATION

ABSTRACT

Distributed parameter drying models such as the Fick's law diffusion model, unlike the lumped parameter model of van Meel whose parameters can be easily estimated by regression, suffer from the difficulty in estimating the parameters of the models quantitatively with accuracy. In the past they were estimated by visual inspection of the theoretical drying curves which fit the experimental drying curve best In this work, a quantitative parameter estimation technique originally suggested by Chavent, is developed by minimizing the integrated squares of error between theoretical and experimental curves over the drying lime (the criterion) subjected to the constraints that the theoretical curve is governed by the constant diffusivity Fick's taw diffusion equation (the constraint). Although the estimation of Fick's law constant diffusivity can be done by using the analytical solution developed by Crank, the use of the Fick's law model here is simply to demonstrate the utility of the proposed technique which can be used in more complex distributed models. The optimization problem is to solve for the adjoint equation for which the value of the Fick's law diffusivity minimizes the criterion. The Lagrangian derivative is solved by using a discrete derivative of the criterion. The theoretical curves are generated by using simple explicit (FSE) and modified Crank-Nicholson (FCR) algorithms The drying of oil palm kernels are used as a case study. Ii is found that the estimated diffusivities of moisture in oil palm kernels range from 0 5 to 5.0 × 10^-10 m²sol;s which are comparable with published data. It is also found that the estimated diffusivity is dependent on the initial moisture content.     

Preparation and Properties of Biodegradable Polymer Film Based on Polyvinyl Alcohol and Tropical Fruit Waste Flour

In this study, two different types of tropical fruit waste flour, rambutan waste flour (RWF) and banana waste flour (BWF), were blended with polyvinyl alcohol (PVOH) by solution casting method. The structure of the blend film was characterised by Fourier Transform Infrared Spectroscopy. The tensile strength and elongation at break of tropical fruit waste flour-filled polyvinyl alcohol were lower, but the tensile modulus was higher, than that of PVOH film. At a similar blend ratio, the tensile properties of the PVOH/RWF film were higher than the PVOH/BWF film, but the PVOH/BWF film showed higher water uptake than PVOH/RWF film.     

Studies on the formation of yttrium iron garnet (YIG) through stoichiometry modification prepared by conventional solid-state method

Y₃Fe₅O₁₂ (YIG) prepared by conventional solid-state method can rarely be of high purity. However, this study suggests that high purity YIG can be produced via conventional solid-state methods, through stoichiometry modification. This is achieved by adding various amounts of excess Fe₂O₃ to control the YIG stoichiometric ratios. In this work, ferrite and yttria were calcined at 1100 °C (for 8 h) and sintered at 1420 °C (6 h). In most samples, the formation of YIG, with YFeO₃ (YIP) and/or Fe₂O₃ as associated phases were detected. Uniform microstructures of YIG are also observed. YIP phase in YIG is found to be inversely related to the addition of excess Fe₂O₃, up to 8 wt%. At above 8 wt% Fe₂O₃ addition, YIP disappears, leaving unreacted excess Fe₂O₃ as a new associated phase. From the investigation, it is safe to conclude that the purity of YIG can be increased with the addition of excess Fe₂O₃.     

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.     

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).     

Synthesis and Characterization of Molecularly Imprinted Polymer Membrane for the Removal of 2,4-Dinitrophenol

Molecularly imprinted polymers (MIPs) were prepared by bulk polymerization in acetonitrile using 2,4-dinitrophenol, acrylamide, ethylene glycol dimethacrylate, and benzoyl peroxide, as the template, functional monomer, cross-linker, and initiator, respectively. The MIP membrane was prepared by hybridization of MIP particles with cellulose acetate (CA) and polystyrene (PS) after being ground and sieved. The prepared MIP membrane was characterized using Fourier transform infrared spectroscopy and scanning electron microscopy. The parameters studied for the removal of 2,4-dinitrophenol included the effect of pH, sorption kinetics, and the selectivity of the MIP membrane. Maximum sorption of 2,4-nitrophenol by the fabricated CA membrane with MIP (CA-MIP) and the PS membrane with MIP (PS-MIP) was observed at pH 7.0 and pH 5.0, respectively. The sorption of 2,4-dinitrophenol by CA-MIP and PS-MIP followed a pseudo–second-order kinetic model. For a selectivity study, 2,4-dichlorophenol, 3-chlorophenol, and phenol were selected as potential interferences. The sorption capability of CA-MIP and PS-MIP towards 2,4-dinitrophenol was observed to be higher than that of 2,4-dichlorophenol, 3-chlorophenol, or phenol.     

Graft Copolymerization of Acrylamide onto Oil Palm Empty Fruit Bunch (OPEFB) Fiber

Grafting of acrylamide (AAm) onto oil palm empty fruits bunch fiber using hydrogen peroxide as initiator and methyl acrylate as comonomer was investigated. The amount of comonomer needed to make grafting of acrylamide possible was determined. The percentage of poly(acrylamide) and the comonomer in the final graft copolymer was estimated by elemental analysis. Results obtained indicated that methyl acrylate facilitated the incorporation of acrylamide monomer onto OPEFB. The reactivity ratios for both monomers were determined by using Fineman–Ross plot. The effects of reaction temperature and period as well as amount of the initiator, solvent, monomer and comonomer on the percentage of grafting at fixed amount of comonomer (11 mmol) were studied. Maximum percentage of grafting was achieved when the amount of initiator and solvent 3.98×10⁻³ mol and 50 mL respectively. The optimum reaction temperature was 50 ^○C and the reaction period was 90 min. Highest percentage of grafting was 232% when 25.6 mmol of acrylamide was used under these optimum conditions. The presence of functional group in the grafted polymer is characterized by infrared spectroscopy and the surface morphology is observed by scanning electron microscopy. Thermoanalytic investigation on OPEFB and OPEFB-g-PAAM were carried out to evaluate the thermal stability and respective activation energy of the materials.