The physicochemical investigation of hydrothermally reduced textile waste and application within carbon-based electrodes.

From Europe PMC via Jisc Publications RouterHistory: ppub 2019-04-01, epub 2019-04-10Publication status: PublishedTextile waste is on the rise due to the expanding global population and the fast fashion market. Large volumes of textile waste are increasing the need for new methods for recycling mixed fabric materials. This paper employs a hydrothermal conversion route for a polyester/cotton mix in phosphoric acid to generate carbon materials (hydrochars) for electrochemical applications. A combination of characterization techniques revealed the reaction products were largely comprised of two major components. The first is a granular material with a surface C : O ratio of 2 : 1 interspersed with phosphorous and titanium proved using energy dispersive X-ray spectroscopy, and the other is a crystalline material with a surface C : O ratio of 3 : 2 containing no phosphorous or titanium. The latter material was found via X-ray diffraction and differential scanning calorimetry to be terephthalic acid. Electrochemical experiments conducted using the hydrochar as a carbon paste electrode demonstrates an increase in current response compared to carbon reference materials. The improved current responses, intrinsically related to the surface area of the material, could be beneficial for electrochemical sensor applications, meaning that this route holds promise for the development of a cheap recycled carbon material, using straightforward methods and simple laboratory reagents

Interfacial surface properties of compression moulded hydrolysed Polyvinyl Acetate (PVAc) using different release materials

Understanding the effect surface production has on polymer properties is important in the design of advanced materials. The aim of this study was to determine how the moulding process affected the rate of hydrolysis and the topography, chemistry and physicochemistry of PVAc moulded, hydrolysed surfaces. Three different mould surface materials were used to produce compression moulded PVAc sheets which were treated with aqueous NaOH at a range of concentrations. The Textile moulded sheet demonstrated the best hydrolysis results. The topography of the moulded sheets was transferred to the surfaces and the Kapton release sheet was visually smooth at lower magnification and demonstrated some pitting at higher magnification. The Teflon surface had features transferred from the coated stainless steel at lower magnifications and linear features at higher magnifications and the textile surface had a wrinkled appearance and irregularly spaced peaks. The release sheet used to mould the PVAc surfaces, affected the physicochemical parameters. The Kapton moulded surface demonstrated the most polar attributes and the Teflon surface the most dispersive. It was clear that the selection of the mould material had an influence on surface properties and hydrolysis of moulded PVAc. Such information is important for engineering design in industrial processes

A comparative assessment of the use of suitable analytical techniques to evaluate plasticizer compatibility

The evaluation of novel phthalate-free plasticisers for PVC formulations is hindered by the lack of a reliable quantitative method for testing plasticizer exudation from PVC formulations. Two methods of improving upon the ASTM D3291 exudation test have been trialed using ATR-FTIR and GC–MS. The results of these methods are compared alongside a study of the glass transition temperatures (Tg) by dynamic mechanical analysis (DMA). FTIR is found to be unsuitable for determining plasticizer exudation as the method is not sufficiently sensitive to detect small changes in plasticizer distribution. Carbonyl peak positions in unstressed samples are instead investigated to determine the strength of interaction between the plasticisers and PVC chain. GC–MS is successfully used to quantify plasticizer exudation that could not be observed visually or by FTIR. Furthermore, these methods show limited correlation to each other, which highlights the importance of testing multiple aspects of compatibility when developing novel plasticisers for use in PVC

Effects of Cationic and Anionic Surfaces on the Perpendicular and Lateral Forces and Binding of Aspergillus niger Conidia

The binding of conidia to surfaces is a prerequisite for biofouling by fungal species. In this study, Aspergillus niger subtypes 1957 and 1988 were used which produced differently shaped conidia (round or spikey respectively). Test surfaces were characterised for their surface topography, wettability, and hardness. Conidial assays included perpendicular and lateral force measurements, as well as attachment, adhesion and retention assays. Anionic surfaces were less rough (Ra 2.4 nm), less wettable (54°) and harder (0.72 GPa) than cationic surfaces (Ra 5.4 nm, 36° and 0.5 GPa, respectively). Perpendicular and lateral force assays demonstrated that both types of conidia adhered with more force to the anionic surfaces and were influenced by surface wettability. Following the binding assays, fewer A. niger 1957 and A. niger 1988 conidia bound to the anionic surface. However, surface wettability affected the density and dispersion of the conidia on the coatings, whilst clustering was affected by their spore shapes. This work demonstrated that anionic surfaces were more repulsive to A. niger 1998 spores than cationic surfaces were, but once attached, the conidia bound more firmly to the anionic surfaces. This work informs on the importance of understanding how conidia become tightly bound to surfaces, which can be used to prevent biofouling

Next Generation Additive Manufacturing: Tailorable Graphene/Polylactic(acid) Filaments Allow the Fabrication of 3D Printable Porous Anodes for Utilisation within Lithium-Ion Batteries

This is the peer reviewed version of the following article: Foster, C. W., Zou, G., Jiang, Y., Down, M. P., Liauw, C. M., Ferrari, A. G., Ji, X., Smith, G. C., Kellyand, P. J., Banks, C. E. (2019). Next Generation Additive Manufacturing: Tailorable Graphene/Polylactic(acid) Filaments Allow the Fabrication of 3D Printable Porous Anodes for Utilisation within Lithium-Ion Batteries. Batteries & Supercaps., 2(5), 448-453, which has been published in final form at https://doi.org/10.1002/batt.201800148. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-ArchivingHerein, we report the fabrication and application of Li-ion anodes for utilisation within Li-ion batteries, which are fabricated via additive manufacturing/3D printing (fused depo- sition modelling) using a bespoke graphene/polylactic acid (PLA) filament, where the graphene content can be readily tailored and controlled over the range 1–40 wt. %. We demon- strate that a graphene content of 20 wt. % exhibits sufficient conductivity and critically, effective 3D printability for the rapid manufacturing of 3D printed freestanding anodes (3DAs); simplifying the components of the Li-ion battery negating the need for a copper current collector. The 3DAs are physicochemcally and electrochemically characterised and possess sufficient conductivity for electrochemical studies. Critically, it is found that if the 3DAs are used in Li-ion batteries the specific capacity is very poor but can be significantly improved through the use of a chemical pre-treatment. Such treatment induces an increased porosity, which results in a 200-fold increase (after anode stabilisation) of the specific capacity (ca. 500 mAhg-1 at a current density of 40 mAg-1). This work significantly enhances the field of additive manufacturing/3D printed graphene based energy storage devices demonstrating that useful 3D printable batteries can be realise

Principal Component Analysis to Determine the Surface Properties That Influence the Self-Cleaning Action of Hydrophobic Plant Leaves

It is well established that many leaf surfaces display self-cleaning properties. However, an understanding of how the surface properties interact is still not achieved. Consequently, 12 different leaf types were selected for analysis due to their water repellency and self-cleaning properties. The most hydrophobic surfaces demonstrated splitting of the νs CH2 and ν CH2 bands, ordered platelet-like structures, crystalline waxes, high-surface-roughness values, high-total-surface-free energy and apolar components of surface energy, and low polar and Lewis base components of surface energy. The surfaces that exhibited the least roughness and high polar and Lewis base components of surface energy had intracuticular waxes, yet they still demonstrated the self-cleaning action. Principal component analysis demonstrated that the most hydrophobic species shared common surface chemistry traits with low intra-class variability, while the less hydrophobic leaves had highly variable surface-chemistry characteristics. Despite this, we have shown through partial least squares regression that the leaf water contact angle (i.e., hydrophobicity) can be predicted using attenuated total reflectance Fourier transform infrared spectroscopy surface chemistry data with excellent ability. This is the first time that such a statistical analysis has been performed on a complex biological system. This model could be utilized to investigate and predict the water contact angles of a range of biological surfaces. An understanding of the interplay of properties is extremely important to produce optimized biomimetic surfaces