Thermally stable antimicrobial PVC/maleimido phenyl urea composites

Four novel antimicro bial maleimido phenyl urea derivatives were synthesized from N-[4-(chlorocarbonyl) phenyl] maleimide with phenyl urea derivatives (p-methyl, o-chloro and p-carboxy). They were characterized by FTIR, ¹H-NMR, mass spectra, elemental analyses and antimicrobial activities. These derivatives were investigated as thermal stabilizers for rigid poly(vinyl chloride) at 180 °C in air by measuring the rate of dehydrochlorination and the extent of discoloration. The results reveal the greater stabilizing efficiency of the investigated derivatives as shown by their longer thermal stability periods (Ts) and lower dehydrochlorination rates in relation to dibasic lead carbonate, cadmium-barium-zinc stearate and n-octyltin mercaptide industrial stabilizers. The stabilizing efficiency increases with the introduction of electron donating substituent groups in the aromatic ring of the stabilizer molecules. Moreover, the investigated stabilizers impart better color stability for the degraded samples as compared with the reference stabilizers.     

Synthesis and characterization of coumarin thiazole derivative 2-(2-amino-1,3-thiazol-4-yl)-3H-benzo[f]chromen-3-one with anti-microbial activity and its potential application in antimicrobial polyurethane coating

Coumarin, thiazole and their respective derivative products are some of the oldest and most commonly known class of nitrogen and sulphur containing compounds. In recent years there has been considerable interest in this coumarin–thiazole derivatives, which have been reported to exhibit significant biological activity and are widely used as pharmaceuticals. They are capable of imparting anti-microbial activity properties when incorporated into polymers and polymer composites. In this research, coumarin–thiazole derivative 2-(2-amino-1,3-thiazol-4-yl)-3H benzo[f]chromen-3-one (compound III), was prepared and its structure was confirmed by means of its spectra data. It was also screened for its anti-microbial activity against eight different micro-organisms when physically incorporated into a polyurethane varnish formula. Experimental coatings were manufactured on a laboratory scale and applied by means of a brush on both glass and steel panels. The results of the biological activity indicated that the polyurethane varnishes containing the 2-(2-amino-1,3-thiazol-4-yl)-3H-benzo[f]chromen-3-one (compound III) derivative, exhibit a very good antimicrobial effect. The molecular modeling study revealed that it is biologically safe, it is active and it fulfills Lipinski's rule of five. The physical and mechanical resistances of the polyurethane varnish formulations were also studied to evaluate any drawbacks associated with the addition of the derivative. The studies indicate that the physical incorporation of compound III actually enhances slightly both the physical and mechanical properties.     

Modification of Rice Starch through Thermal Treatment with Urea

Modification of starch with urea was carried out at 165 °C according to solid state, paste and film techniques. With the solid state and paste techniques the extent of the reaction, expressed as % N, increased by increasing the time of treatment. Samples prepared by the film technique showed, during the first 15 min reaction time, significantly higher nitrogen content which, however, decreased by prolongation of the treatment. Infra-red spectrum of the reaction products indicated involvement of both starch and urea in a chemical reaction. Examination of the swelling properties of the products revealed that these properties are dependent upon the technique used for preparation rather than the extent of the reaction. Samples prepared by the paste and film techniques acquired higher apparent viscosity than those prepared by the solid state technique irrespective of the rate of shear. For a given rate of shear, the apparent viscosity increases by increasing the temperature.     

Chitosan Functionalized with Carboxyl Groups as a Recyclable Biomaterial for the Adsorption of Cu (II) and Zn (II) Ions in Aqueous Media

The modification of chitosan represents a challenging task in obtaining biopolymeric materials with enhanced removal capacity for heavy metals. In the present work, the adsorption characteristics of chitosan modified with carboxyl groups (CTS-CAA) towards copper (II) and zinc (II) ions have been tested. The efficacy of the synthesis of CTS-CAA has been evaluated by studying various properties of the modified chitosan. Specifically, the functionalized chitosan has been characterized by using several techniques, including thermal analyses (differential scanning calorimetry and thermogravimetry), spectroscopies (FT-IR, XRD), elemental analysis, and scanning electron microscopy. The kinetics and the adsorption isotherms of CTS-CAA towards both Cu (II) and Zn (II) have been determined in the aqueous solvent under variable pH. The obtained results have been analyzed by using different adsorption models. In addition, the experiments have been conducted at variable temperatures to explore the thermodynamics of the adsorption process. The regeneration of CTS-CAA has been investigated by studying the desorption process using different eluents. This paper reports an efficient protocol to synthesize chitosan-based material perspective as regenerative adsorbents for heavy metals.     

Technological Evaluation of Nitrogen Containing Starch Derivatives as Sizing Agents

The structural changes brought about by introducing different nitrogen containing groups via cyanoethylation, carbamoylethylation and carbamation in the molecules of rice and maize starches and oxidized starches derived thereof and the onset of these changes on the technical properties of yarns sized with such starch products were investigated. It was found that the apparent viscosity of pastes prepared from those products depends on the nature of starch, the degree of oxidation prior to chemical modification, the nature of modification as well as the measuring conditions, i. e. the rate of shear and temperature. Cotton yarns sized using these starch derivatives were measured for yarn number, tensile strength, C.V.%, elongation at break and C.V.% in elongation. Besides, the weavability test expressed as the minimum number of cycles due to abrasion (St₁) and average number of cycles due to abrasion (St₆) were investigated. A comparison among modified starches prepared from rice starch would reveral that the highest value of St₁ is obtained with yarns sized using carbamoylethylated sample derived from unoxidized starch. With maize starch, on the other hand, the highest value of St₁ is obtained with cotton yarns sized using carbamoylethylated starch derived from starch oxidized by 1 g/l active chlorine.     

Chemical Modification of Guaran Gum. Part 3: Carboxymethylation in non-Aqueous Medium

Guar gum was isolated from the seeds and subjected to modification via non-aqueous carboxymethylation. Highly substituted carboxymethyl guaran derivatives could be obtained via repeating the reaction four times, where a product of degree of substitution (D.S.) 2.07 was obtained indicating that the free hydroxyl groups of both glucose and mannose (which form the main constituents of guaran) can react with monochloro acetic acid. The modification increases the solubility of the gum in cold water, and increases the stability of its pastes to microorganisms. Pastes of these derivatives are characterized by non-Newtonian pseudoplastic behaviour regardless of their D.S. or the measuring temperature, while their apparent viscosity decreases by increasing the D.S. and/or the measuring temperature.     

Amphiphilic Pentablock Copolymers Prepared from Pluronic and ε-Caprolactone by Enzymatic Ring Opening Polymerization

Amphiphilic copolymers are appealing materials because of their interesting architecture and tunable properties. In view of their application in the biomedical field, the preparation of these materials should avoid the use of toxic compounds as catalysts. Therefore, enzymatic catalysis is a suitable alternative to common synthetic routes. Pentablock copolymers (CUC) were synthesized with high yields by ring-opening polymerization of ε-caprolactone (ε-CL) initiated by Pluronic (EPE) and catalyzed by Candida antarctica lipase B enzyme. The variables to study the structure–property relationship were EPEs’ molecular weight and molar ratios between ε-CL monomer and EPE macro-initiator (M/In). The obtained copolymers were chemically characterized, the molecular weight determined, and morphologies evaluated. The results suggest an interaction between the reaction time and M/In variables. There was a correlation between the differential scanning calorimetry data with those of X-ray diffraction (WAXD). The length of the central block of CUC copolymers may have an important role in the crystal formation. WAXD analyses indicated that a micro-phase separation takes place in all the prepared copolymers. Preliminary cytotoxicity experiments on the extracts of the polymer confirmed that these materials are nontoxic.     

Structural Control of NiO–YSZ/LSCF–YSZ Dual‐Layer Hollow Fiber Membrane for Potential Syngas Production

The objective of this study was to fabricate dual‐layer hollow fiber as a microreactor for potential syngas production via phase inversion‐based co‐extrusion/cosintering process. As the main challenge of phase inversion is the difficulty to obtain defect‐free fiber, this work focuses on the effect of the fabrication parameters, that is, nonsolvent content, sintering temperature and outer‐layer extrusion rate, on the macrostructure of the produced hollow fiber. SEM images confirm that the addition of nonsolvent has successfully minimized the finger‐like formation. At high sintering temperature, more dense hollow fiber was formed while outer‐layer extrusion rate affects the outer layer thickness.     

Vanadium oxide supported γ-alumina with bimodal porous structure for intra-particle diffusion enhancement in styrene oxidation reaction

Porous γ-alumina with well arranged secondary mesopores has been contrived using nanosized templating units. The pore size of templated mesopores is precisely controlled as the pore shrinkage is insignificant. The primary pore diameter is ca. 4 nm and the secondary pore diameter is ca. 50 nm. The porous material was characterized using N₂ adsorption/desorption, TEM, XRD and FT-IR. γ-alumina with bimodal pore size distribution shows improved intra-particle diffusion compared to γ-alumina with unimodal pore size distribution in a simple dye adsorption test. γ-alumina with different porous structures were then impregnated with vanadium oxide for catalytic effect comparison. It was perceived that secondary pores improve the styrene oxidation rate after the conversion of styrene reaches 30%.     

Composite Nanoarchitectonics of Graphene Oxide for Better Understanding on Structural Effects on Photocatalytic Performance for Methylene Blue Dye

Journal of Inorganic and Organometallic Polymers and Materials - The fabrication of graphene/graphene oxide bounded metal nanostructures, to form hybrid composites, and their utilization for the...