Academic literature on the topic 'Acrylonitrile Environmental aspects'

The pretreatment of ABS (acrylonitrile-butadiene-styrene) plastics prior to metallization has been generally performed with strong acids, such as sulfuric, chromic, or potassium-permanganate acid. However, conventional wet-chemical pretreatment presents inherent environmental and safety problems to consider. In particular, the presence of Cr+6 imposes a serious environmental threat. Therefore, in this study, aspects of pretreatment, using the photocatalytic reaction in TiO2 sol, were investigated as a replacement for wet-chemical pretreatment. Surface characterization, before and after the pretreatment, was examined by X-ray photoelectron spectroscopy and scanning electron microscopy. A copper film was deposited by electroless plating, and the adhesion strength between the deposited film and ABS plastics was evaluated by the cross-cut tape test (ISO 2409). When ABS plastics were pre-treated in TiO2 sol, the adhesion strength was improved to levels obtained using a strong acid solution.

Purpose In this paper, the authors propose an experimental set-up to study the chemical vapour polishing technique confining pure dimethylketone atmosphere at a fixed temperature in a vacuum chamber. The purpose of this paper is to improve conventional vapour treatments lowering the amount of solvent, lowering time and temperature needed and improving the environmental impact of the technique. Design/methodology/approach A factorial design of experiments is adopted to understand the effect of the treatment on roughness and on the surface morphology of treated specimens. Findings The proposed method improves several aspects of well-known methods based on water–dimethylketone liquid solution such as: no interaction between water and workpiece and higher capability of process management. It also improves several aspects of well-known methods based on vapour, lowering the amount of solvent, time and temperature compared to conventional vapour treatments. Originality/value Chemical vapour polishing is a well-known technique for smoothing additive manufactured acrylonitrile butadiene styrene (ABS) parts. Several data and users' experiences are available on the Web about this topic. In recent scientific literature, a few papers are available about this topic, dealing with how process parameters affect the final surface roughness. In the present paper, the authors propose to improve the process performing the process using dimethylketone into a vacuum chamber. The main advantages are the significant reduction of the solvent needed to perform the process and lower time needed to obtain same results as atmospheric pressure treatments.

This study proposes a hydrophobic and hydrophilic aliphatic diblock copolymer wherein the hydrophobic block contains glycidyl methacrylate (GMA) units that are distanced by poly(acrylonitrile) (PAN) segments to fabricate a proton exchange membrane (PEM). This diblock copolymer also known as ionomer due to the hydrophilic block comprising 3-sulfopropyl methacrylate potassium salt (SPM) block. The diblock copolymer was synthesized in the one-pot atom transfer radical polymerization (ATRP) synthesis. Subsequently, the membrane was fabricated by means of solution casting in which an organic diamine, e.g., ethylene diamine (EDA), was introduced to crosslink the diblock copolymer chains via the addition of amine to the epoxide group of GMA. As a result, the PEM attained possesses dual continuous phases, in which the hydrophobic domains are either agglomerated or bridged by the EDA-derived crosslinks, whereas the hydrophilic domains constitute the primary proton conducting channels. The in-situ crosslinking hydrophobic block by using a hydrophilic cross-linker represents the merit aspect since it leads to both improved proton conductivity and dimensional stability in alcohol fuel. To characterize the above properties, Nafion® 117 and random copolymer of P(AN-co-GMA-co-SPM) were used as control samples. The PEM with the optimized composition demonstrates slightly better fuel cell performance than Nafion 117. Lastly, this diblock ionomer is nonfluorinated and hence favors lowering down both material and environmental costs.

The article is devoted to the issue of a low sweep efficiency in the heterogeneous terrigenous reservoirs containing remaining oil. Water plugging operations that redirect the injection fluid flows into unswept zones, are one approach to enhancing the oil recovery in these reservoirs. The commonly used chemical reagents in these treatments are acrylate polymer solutions. The polymer solutions must reach the target water-saturated zones and form a strong gel barrier there. Furthermore, the polymer compositions should have a low initial viscosity to provide a good injectivity and penetration ability. Therefore, the methods of adjusting the gelation time are necessary. There are numerous studies in modern scientific society devoted to the study of water-plugging polymer compositions. However, aspects, such as the effect of the hydrogen index on gelation, have received insufficient attention. In this paper, we describe the features of the developed polymer composition, based on a hydrolyzed polymer of acrylonitrile with a controlled gelation time for the chemically enhanced oil recovery. The component composition and the concentration levels were selected, based on the alterations in the hydrogen index of the polymer solution. It was scientifically proven that by adhering to a neutral hydrogen index, it is possible to improve the properties of the polymer composition. Moreover, using a model of a heterogeneous reservoir, it was confirmed that the proposed polymer composition achieves selective plugging. As a result of the polymer gel treatment, the water cut decreased by 4% and the displacement coefficient of oil increased by 20%, in comparison with the effect of the original composition without a gel-time modifier.