Thermally stable antimicrobial polyvinylchloride/maleimido aromatic hydrazide composites

Antimicrobial novel substituted maleimido aromatic hydrazides were synthesized from N‐[4‐(chlorocarbonyl) phenyl] maleimide with salicylhydrazide, p‐aminobenzohydrazide, or p‐aminosalicylhydrazide. They were characterized by Fourier transform infrared (FTIR), hydrogen‐1 nuclear magnetic resonance (¹H‐NMR), mass spectra, elemental analyses, and antimicrobial activities. These derivatives were investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C in air by measuring the rate of dehydrochlorination, the extent of discoloration, and the changes that occurred in the molecular masses of the degraded PVC samples. The previously reported stabilizing efficiency data of a nonsubstituted derivative, which was synthesized from N‐[4‐(chlorocarbonyl) phenyl] maleimide with benzohydrazide, is also given for comparison. The results reveal the greater stabilizing efficiency of the investigated derivatives as shown by their longer thermal stability (Ts) periods 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. A synergistic effect is achieved when the materials under investigation were mixed in various weight ratios with any of the reference stabilizers, reaching its maximum at equivalent weight ratio of the investigated stabilizer to the reference one. J. VINYL ADDIT. TECHNOL., 22:247–258, 2016. © 2014 Society of Plastics Engineers     

Effects of diagenesis on the geomechanical and petrophysical aspects of the Jurassic Bir El-Maghara and Masajid carbonates in Gebel El-Maghara,North Sinai,Egypt

Bulletin of Engineering Geology and the Environment - In the present study, the Jurassic Bir El-Maghara and Masajid Formations in North Sinai are subjected to a detailed microfacies analysis to...     

Synthesis of a novolac‐based 3‐aminopropylsiloxane resin and its application for the removal of Cu2+, Cr3+, and Ni2+ from electroplating wastewater

Novolac resin was modified with 3‐aminopropyltrimthoxysilane to obtain phenol‐formaldehyde‐aminopropylsiloxane resin (PF‐APS). Fourier transformation infra‐red spectra, thermogravimetric analysis, elemental analysis, and pH‐metric titration were used to characterize PF‐APS. Its chemical formula was suggested to be C₁₄H_12.49N_0.1O₂Si_0.1. The resin shows high experimental metal ions uptake capacity within short time of equilibration. The metal capacity was determined by atomic absorption spectrometry to be 0.787 mEq Cu/g. Maximum separation efficiencies of Cu²⁺, Cr³⁺, and Ni²⁺ from aqueous solutions on PF‐APS were at pH 8.0 and time of stirring 60 min; 94.0%, 90.8%, 83.2%, respectively. No significant interference from the background ions Na⁺, Cl^?, and was observed on the separation process. The heavy metal ions were eluted using 0.01 mol L^?1 EDTA at 65°C releasing >94% of the separated metal ions. The method of separation was applied successfully to remove the heavy metal ions Cu²⁺, Cr³⁺, and Ni²⁺ from electroplating wastewater from Dekirnis, Dakahlia Governorate, Egypt. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40993.     

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.     

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.     

Mechanism of action of Melaleuca armillaris (Sol. Ex Gaertu) Sm. essential oil on six LAB strains as assessed by multiparametric flow cytometry and automated microtiter-based assay

Little is known concerning the effects of essential oils (EOs) against lactic acid bacteria (LAB), either of the human gastrointestinal microflora or those involved in industrial processes. GC and GC/MS analysis of Melaleuca armillaris EO resulted in the identification of 68 compounds comprising 99.6% of the oil. Eucalyptol (1,8-cineole) was the major compound (68.9%) and the composition was largely dominated by the oxygenated monoterpenes fraction (77.3%). The anti-LAB activities of the EO were first checked by the disc diffusion assay. In a second phase, time-survival kinetics of each strain incubated with increasing concentrations of the EO (0.25, 2.5, 5 and 25 μg/ml) were established using an automated microtiter assay (Bioscreen C). Bacteriostatic or bactericidal effects were noticed depending on the studied strain and on the applied concentration of the EO. The mathematical modelling of the kinetics showed that in presence of increasing concentrations of M. armillaris EO, the lag phases of growth were extended (0.69%–97.5%) and both the growth rate and final cell density were reduced. Variations depending on the strain were noticed.