Natural fiber reinforced polymer composites

The use of natural fibers as a reinforcement for various materials was recorded already in ancient Egypt; however, their rediscovery can be dated to the beginning of 20th century. Currentspecial issueisdevoted to theroleofnatural fibersas reinforcements for various biodegradable and nonbiodegradable polymer matrices. The application of natural fillers can be seen as an approach to adjust material performance of polymer composites supposing that filler/matrix interactions will be optimized and a hygroscopicity of natural fillers will be hindered. This special issue contains 16 papers that highlight a number of reasons for applications of natural fillers in polymer composites. In recent years the discussion about a balance in carbon footprint increased an attractiveness of natural fibers/fillers derived from agricultural sources predominantly from one-year plants

Pd nanoparticles confined in mesoporous N-doped carbon silica supports: a synergistic effect between catalyst and support

Palladium nanoparticles of similar size were deposited on different supports, layers of carbon materials (with and without nitrogen doping) on the surface of a MCF (mesocellular foam) silica. For the generation of the N-doped carbon coatings, three different N sources were used to also investigate a possible influence of the N-doped carbon precursor and thus the structure of the N-doped carbons on their performance as catalyst support. These catalysts were tested for the Suzuki coupling and hydrogenation reactions. For the Suzuki reaction, the carbon coatings showed to increase dramatically the stability of the MCF material. Furthermore, when N-doped carbon coatings were applied, strong improvement of the stability of the catalysts was observed due to an enhanced interaction between metal nanoparticles and the support, preventing metal particle growth. In hydrogenation reactions, the presence of the N-doped carbon coating on the silica support increases the adsorption of aromatic compounds causing an enhancement of the catalytic activity of Pd NPs when compared to the non-doped supports.TU Berlin, Open-Access-Mittel - 2020DFG, 390540038, EXC 2008: UniSysCa

Electrogenerated N-Heterocyclic Carbene in Ionic Liquid: An Insight into the Mechanism of the Oxidative Esterification of Aromatic Aldehydes

An N-heterocyclic carbene (NHC), generated by cathodic reduction of BMImBF4, mediates the oxidative esterification of aromatic aldehydes with organic bromides in the corresponding ionic liquid as solvent. The product recovery by simple extractive work-up with diethyl ether allowed the ionic liquid to be recycled up to 9 times for subsequent electrolyses, with no significant loss in the product yield. The isolation of an intermediate, whose structure was confirmed by synthesis and transformation into the ester, provided the key for a mechanistic insight into the reaction. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Tuning the electronic environment of cations and anions using ionic liquid mixtures

Electrostatic interactions are ubiquitous in ionic liquids and therefore, the electronic environment (i.e. the distribution of electron density) of their constituent ions has a determining influence on their properties and applications. Moreover, the distribution of electron density on atoms is at the core of ionic liquid molecular dynamics simulations. In this work, we demonstrate that changing the composition of ionic liquid mixtures can tune the electronic environment of their constituent ions, both anions and cations. The electronic environment of these ions can be monitored by measuring the characteristic electron binding energies of their constituent atoms by X-ray photoelectron spectroscopy (XPS). The possibility to fine tune, in a controlled way, the electronic environment of specific ions provides an invaluable tool to understand ionic liquid properties and allows the design of ionic liquid mixtures towards specific applications. Here, we demonstrate the power of this tool by tuning the electronic environment of a catalytic centre, and consequently its catalytic activity, by the use of ionic liquid mixtures

Investigation on Aromaticity Index and Double-Bond Equivalent of Aromatic Compounds and Ionic Liquids for Fuel Desulphurization

Aromaticity index (AI) and double-bond equivalent (DBE) were studied to seek a simpler approach in identifying suitable ionic liquids for the desulphurization process. Manifestation of interaction mechanism by COSMO-RS and Raman spectroscopy is discussed. The findings demonstrate that AI and DBE calculations can be used to analyze and arrogate potential combination of cation and anion for fuel desulphurization purposes

Computational approaches to understanding reaction outcomes of organic processes in ionic liquids

This review considers how various computational methods have been applied to explain the changes in reaction outcome on moving from a molecular to an ionic liquid solvent. Initially, different conceptual approaches to modelling ionic liquids are discussed, followed by a consideration of the limitations and constraints of these approaches. A series of case studies demonstrating the utility of computational approaches to explain processes in ionic liquids are considered; some of these address the solubility of species in ionic liquids while others examine classes of reaction where the outcome in ionic liquids can be explained through the application of computational approaches. Overall, the utility of computational methods to explain, and potentially predict, the effect of ionic liquids on reaction outcome is demonstrated

Poly(thioether) vitrimers via transalkylation of trialkylsulfonium salts

Vitrimers are permanently cross-linked organic polymers that can be reshaped, molded, and recycled without loss of network integrity. Herein, we report poly(thioether) networks, prepared through a straightforward thiol-ene photopolymerization, that can be turned into catalyst-free vitrimer materials by partial alkylation of the thioethers (1-10%) to the corresponding trialkylsulfonium salts. Based on a classical S(N)2-type substitution, the resulting polyionic networks can be reshaped upon heating via swift transalkylation reactions. This novel exchange reaction for the design of vitrimers was studied both on low MW model compounds as well as on a material level. In addition, we demonstrated the recycling of these networks without significant loss of mechanical properties

Versatile continuous pH monitoring barcode system based in ionogels

The online monitoring of pH level in different environments like bio-engineering [1] and chemistry [2] is vital for the control and well behaviour of the whole industrial process. Still exist the demand of miniaturised, versatile and autonomous systems which do not require of sensor calibration, replacement and manual attention over a long operational interval. In this abstract we present an innovative miniaturisable system for continuously measurement of pH solutions and vapours streams during chemical or biological processes. It consists on a simple barcode sensor with several pH dyes doped in an ionogel matrix. This ionogel is a hybrid material fabricated from an hydrogel polymer (N-isopropylacrylamide and N,N-methylene-bis(acrylamide) ratio 100:5) and an ionic liquid (Trihexyltetradecylphosphonium dicyanoamide). The barcode sensor consists of nineteen independent micro-wells (120 mm by 50 m) fabricated in poly(methyl methacrylate) and pressure-sensitive adhesive in three layers using a CO2 ablation laser. Different optically responsive molecular recognition ligands (pH-dyes) were incorporated in the ionogel matrix during monomers photo-polymerisation within each of the micro-wells generating a pH-sensor array for specific sensing applications like colorimetric, environmental or chemical sensing, Figure 1. It was observed that no leaching of pH dyes occurred during experiments and that the ionogel material was impressively robust under harsh conditions (pH:1 to pH: 14). The result is a sensing barcode which is able to generate a characteristic fingerprint-type colour of response within a single “snapshot” for different pH solutions and vapours. Moreover the pH response can be monitoring continuously and the barcode is reusable at least fifty times without sensitivity withdrawing