Effect of the structure of polymer inclusion membranes on zn(II) transport from chloride aqueous solutions

This article presents application of polymer inclusion membranes (PIM) containing polymer matrices: cellulose triacetate (CTA) or poly(vinyl) chloride (PVC), o‐nitrophenyloctyl ether (NPOE) as a plasticizer and phosphonium ionic liquids, i.e., trihexyltetradecylphosphonium chloride (Cyphos IL 101), bis(2,4,4‐trimethylpentyl)phosphinate (Cyphos IL 104) and tributyltetradecylphosphonium chloride (Cyphos IL 167), as carriers for Zn(II) transport from chloride medium. Cyphos IL167 application as an ion carrier in PIMs is reported for the first time. The membrane composition is found to affect Zn(II) transport significantly. SEM and AFM images show the differences in the surface morphology of PVC and CTA based membranes. Better transport abilities of CTA membranes (Zn(II) recovery factors exceed 80%) compared with those of PVC, indicate that the structural differences between the two polymers play a crucial role for the membrane permeability. The best initial flux and permeability coefficient are obtained for the membranes with Cyphos IL 101 and Cyphos IL 104 as carriers. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42319.     

Rhodium(I) complex catalyst immobilized on terpolymers of N‐vinylpyrrolidinone and 1‐vinylimidazole

The hydrosilylation of cyclohexanone and acetone with triethysilane and diphenysilane catalyzed by polymer‐supported Rh(I) complex has been investigated. Two terpolymers of styrene, divinylbenzene, and 1‐vinylimidazole (S/DVB/VI) or N‐vinylpyrrolidinone (S/DVB/NVP) were used as the catalysts supports. Physical characterization of these materials has involved the measurements of the structural parameters in the dry and swollen states by DSC, the nitrogen BET adsorption method and inverse steric exclusion chromatography ISEC. From these results it can be concluded that the original polymer structure has been changed during the complex attachment giving rise to materials of higher porosity. X‐ray photoelectron spectroscopy XPS, IR, and AAS spectroscopy were used to characterization of heterogeneous complexes before and after use. The effect of the morphology of the support on the catalytic properties of the polymer‐supported Rh(I) species was tested in the hydrosilylation of ketones and correlated with the reaction mechanism. It was demonstrated that the high selectivity of homogeneous rhodium complex toward the silyl ethers can be partially reversed to the dehydrogenative silylation products by a proper choice of polymer support with favorable microporous structure. Recycling tests demonstrated high stability of the supported catalysts during prolonged use. The constant selectivity of the supported catalysts demonstrated during recycling experiments showed that they could be useful for practical application. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

UV‐assisted screen‐printing of flat textiles

An approach to printing of flat textiles is presented in this work. A screen‐printing method was applied on a cotton fabric. An aqueous printing paste was prepared from thickening and crosslinking agents and an ultraviolet‐sensitive tetrazole ring‐based compound of 2,3,5‐triphenyltetrazolium chloride or nitrotetrazolium blue chloride. After the printing process, a pattern was just visible with the naked eye. The development of colour occurred after exposure of the textile to ultraviolet light of 253.7 nm and was caused by the transformation of 2,3,5‐triphenyltetrazolium chloride or nitrotetrazolium blue chloride salts into the corresponding formazans, which are insoluble in water. The printed designs were resistant to washing. The stability of the colour of the samples is discussed in the case of prolonged irradiation, both with ultraviolet light of 253.7 nm and with daylight. This method of printing is a recent proposition for creative textile designing. It also seems to indicate a likely type of dye that may be further developed as potentially attractive for ultraviolet‐assisted printing or dyeing of textiles.     

Changes in Molecular Characteristics of Cereal Carbohydrates after Processing and Digestion

Different extraction, purification and digestion methods were used to investigate the molecular properties of carbohydrates in arabinoxylan and β-glucan concentrates, dietary fiber (DF) rich breads and ileum content of bread fed pigs. The breads studied were: a low DF wheat bread (WF), whole meal rye bread (GR), rye bread with kernels (RK), wheat bread supplemented with wheat arabinoxylan concentrate (AX) and wheat bread supplemented with oat β-glucan concentrate (BG). The weight average molecular weight (M_w) of extractable carbohydrates in β-glucan concentrate decreased eight-fold after inclusion in the BG bread when exposed to in vitro digestion, while the M_w of purified extractable carbohydrates in AX bread was reduced two-fold, and remained almost unaffected until reaching the terminal ileum of pigs. Similarly, the M_w of purified extractable carbohydrates in GR and RK bread was not significantly changed in the ileum. The AX bread resulted in the highest concentration of dissolved arabinoxylan in the ileum among all the breads that caused a substantial increased in ileal AX viscosity. Nevertheless, for none of the breads, the M_w of extractable carbohydrates was related neither to the bread extract nor ileal viscosity.     

Relaxation processes and intermolecular interactions in PVME hydrogels in sub-zero temperatures: Glass transition and pre-melting of ice

The phase transition observed by various methods in poly(vinyl methyl ether)/water systems at around 18 °C has been assigned by some investigators to the pre-melting of water and by others to a glass transition of the polymer. In this study, broadband dielectric spectroscopy and temperature modulated differential scanning calorimetry were used to identify this transition in radiationally crosslinked poly(vinyl methyl ether) hydrogels, as well as to analyse sub-zero relaxation processes in such a three-phase (polymer/ice/liquid water) system. The process at 18 °C was related to the pre-melting of water induced by the segmental motions of the polymer; however, it was seen to be one transition due to the cooperative motions of both compounds. The atypical (two regimes) temperature dependence of the segmental motion process was observed and was related to confinement of the polymer chains between ice clusters below approximately ?24 °C; furthermore, the main dielectric process of hexagonal ice was identified and a Maxwell-Wagner effect was observed.     

The assessment of microorganism growth in the membrane distillation system

Growth of microorganism in the membrane distillation (MD) system has been evaluated, and their presence on the membrane surface was studied using scanning electron microscopy (SEM) coupled with energy dispersion spectrometry (EDS). The membrane samples were collected from MD modules used for the following applications: concentration of salts and acids, production of demineralized water from tap water, separation of ethanol from fermentation broth in a membrane bioreactor and treatment of saline wastewater containing Pseudomonas and Streptococcus faecalis bacteria and Penicillium and Aspergillus fungi. The MD experiments were performed with polypropylene capillary membranes. SEM examinations of the membranes used for the treatment of saline wastewater indicated a significant amount of S. faecalis bacteria and Aspergillus fungi. The polypropylene membranes used did not reject S. faecalis bacteria, which were detected on the membrane surface on the distillate side. The presence of fungi in the membrane pores was observed only on the feed side. The contamination of the membrane surface by yeast cells was not observed in the case of the membrane bioreactor operated over one year. The running conditions of the MD process (such as elevated temperature, significant salt concentrations and low pH values) inhibited the growth of microorganism in the MD system.     

Activation of bifunctional coupling agents in fiberglass/polyethylene composites by electron beam

Electron beam (EB) radiation was investigated as a means to initiate coupling between the fiberglass and plastic phases in fiberglass/polyethylene plastic composites using two bifunctional compounds, 12‐azido‐1‐diazo‐2‐dodecanone (A) and 1‐diazo‐17‐octadecene‐2‐one (B). Chemical studies reveal that EB radiation has the potential to bind both of these compounds to fiberglass. Fiberglass coated with either A or B shows reduced values of percentage recovery upon exposure to EB, indicating a reaction between these compounds and the glass surface. However, even 400 kGy of radiation was not as effective as a heat treatment for 45 min at 150°C. To test the effectiveness of EB radiation to couple these compounds to polyethylene, fiberglass samples were heat‐treated with compounds A and B, followed by extrusion mixing with polyethylene, and exposure of molded tensile and impact samples to EB radiation. Compound B showed the best overall ability to couple with the polyethylene matrix, but a 400‐kGy dose was necessary to bring about substantial coupling. At 400 kGy, samples containing B showed a 23% improvement in tensile properties and a 30% change in Izod impact. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2579–2594, 2002     

Bifunctional coupling agents for improved mechanical properties in fiberglass/polyethylene composites

Two bifunctional compounds, 12‐azido‐1‐diazo‐2‐dodecanone (A) and 1‐diazo‐17‐octadecene‐2‐one (B), show an ability to act as coupling agents in fiberglass/polyethylene composites. Under appropriate conditions the diazoketone functional groups in both A and B react with hydroxyl groups on a fiberglass surface, whereas the azide group in A and the alkene group in B form bonds with the plastic matrix during processing. FTIR and NMR spectroscopy were used to study the decomposition of each of these compounds under heat and UV light. Each treatment resulted in a relatively fast decomposition of the diazoketone functional group, along with a slower reaction of the azide and alkene groups. Thus it was possible to react the diazoketone end of these compounds with a fiberglass surface, without affecting the azide or alkene functional groups on the other ends of the molecules. In samples of treated fiberglass containing compounds A or B and mixed by extrusion with polyethylene, the mechanical properties of the composites had improved properties over composites containing untreated samples of fiberglass. With A as the coupling agent, both the tensile properties and Izod impact showed changes that indicated that a bifunctional bridge was formed between the fiberglass and polyethylene phases. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2562–2578, 2002     

Effect of butyl rubber type on properties of polyamide and butyl rubber blends

Polyamide‐12 was blended with butyl rubber, bromobutyl rubber, and chlorobutyl rubber with and without a sulfur curing system. Mechanical properties for dynamically vulcanized blends generally exceed those made with no vulcanization. Chlorobutyl‐containing blends prepared by dynamic vulcanization have higher tensile strength and elongation at break values in comparison to those made from other butyl rubbers. For a variety of polyamide/rubber blends made by dynamic vulcanization, there is very little effect of rubber percentage unsaturation and Mooney viscosity on the mechanical properties of the blends. In chlorobutyl‐containing blends prepared by dynamic vulcanization, the swelling index values attributed to the rubber portion decrease as rubber content decreases, and it is likely that the polyamide phase completely surrounds the rubber particles at compositions exceeding approximately 25% polyamide. Swelling index results can be correlated with elongation at break values for similar blends. The results of differential scanning calorimetry suggest that the polyamide phase is not a neutral component in high shear mixing with butyl rubbers with or without curing agents. Rheological studies indicate strong non‐Newtonian behavior for all blends of polyamide‐12 with butyl rubbers. Scanning electron microscopy on polyamide‐12/butyl rubber blends indicates compatibility for butyl rubbers in the order of chlorobutyl > bromobutyl > butyl rubber. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1423–1435, 2004