An alternative self-assembly strategy based on low-interactions for the fabrication of graphene-based sponges, using M13 bacteriophage as a cross-linking agent.
M13 bacteriophage is a well-established versatile nano-building block, which can be employed to produce novel self-assembled functional materials and devices. Sufficient production and scalability of the M13, often require a large quantity of the virus and thus, improved propagation methods characterised by high capacity and degree of purity are essential. Currently, the ‘gold-standard’ is represented by infecting Escherichia coli cultures, followed by precipitation with polyethylene glycol (PEG). However, this is considerably flawed by the accumulation of contaminant PEG inside the freshly produced stocks, potentially hampering the reactivity of the individual M13 filaments. Our study demonstrates the effectiveness of implementing an isoelectric precipitation procedure to reduce the residual PEG along with FT-IR spectroscopy as a rapid, convenient and effective analytic validation method to detect the presence of this contaminant in freshly prepared M13 stocks.
In general, the electro-spinning of lignin requires it to be functionalised and/or blended with synthetic or natural polymers. This paper reports on the use of solvent fractionated lignin-lignin blend to electro-spin BioChoice softwood Kraft lignin. The blend consisted of acetone-soluble and ethanol-soluble lignin in a binary solvent of acetone and DMSO. Solvent fractionation was used to purify lignin where the ash content was reduced in the soluble lignin fractions from 1.24 to ~ 0.1%. The corresponding value after conventional acid-washing in sulphuric acid was 0.34%. A custom-made electro-spinning apparatus was used to produce the nano-fibres. Heat treatment procedures were developed for drying the electro-spun fibres prior to oxidation and carbonisation; this was done to prevent fibre fusion. The lignin fibres were oxidised at 250 °C, carbonised at 1000 °C, 1200 °C and 1500 °C. The cross-section of the fibres was circular and they were observed to be void-free. The longitudinal sections showed that the fibres were not fused. Thus, this procedure demonstrated that solvent fractionated lignin can be electro-spun without using plasticisers or polymer blends using common laboratory solvents and subsequently carbonised to produce carbon fibres with a circular cross-section.
The search precursors that are bio-based, renewable and biodegradable has attracted significant attention due to increased environmental awareness. Recently, nano-crystalline cellulose (NCC) has been considered as a potential precursor to produce carbon fibre owing to its high crystallinity and excellent mechanical properties. However, its crystallinity prevents it from being dissolved in comment solvents. The main aims of this study were: (i) to acetylate NCC to improve its compatibility with cellulose acetate and (ii) to produce wet-spun cellulose acetate fibres reinforced acetylated and unacetylated NCC. In this study, rod-like particles of NCC with diameters in the range 2.0-4.8 nm and lengths of 46-114 nm were characterised using a Transmission Electron Microscope (TEM). The carbonyl (C=O) group of the acetyl group was confirmed using Fourier Transmission Infrared (FTIR), and the crystallinity of NCC was characterised using X-Ray Diffraction (XRD). The crystallinity indicates of the NCC before and after acetylation were 78% and 68% respectively. The morphology of wet-spun cellulose acetate reinforced acetylated NCC was smoother than reinforced NCC. The acetylation on NCC increased its compatibility with the polymer matrix.
In general, the electro-spinning of lignin requires it to be functionalised and/or blended with synthetic or natural polymers. This paper reports on the use of solvent fractionated lignin-lignin blend to electro-spin BioChoice® softwood Kraft lignin. The blend consisted of acetone-soluble and ethanol-soluble lignin in a binary solvent of acetone and DMSO. Solvent fractionation was used to purify lignin where the ash content was reduced in the soluble lignin fractions from 1.24% to ~0.1%. The corresponding value for conventional acid-washing in sulphuric acid was 0.34%. A custom-made electro-spinning apparatus was used to produce the nano-fibres. Heat treatment procedures were developed for drying the electro-spun fibres prior to oxidation and carbonisation; this was done to prevent fibre fusion. The lignin fibres were oxidised at 250⁰C, carbonised at 1000⁰C and 1500⁰C. The cross-section of the fibres was circular and they were observed to be void-free. The longitudinal sections showed that the fibres were not fused. Thus, this procedure demonstrated that solvent fractionated lignin can be electro-spun without using plasticisers or polymer blends using common laboratory solvents and subsequently carbonised to produce carbon fibres with a circular cross-section.
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