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There is much interest in the use of deoxyribonucleic acid (DNA) for applications in the field of molecular electronics and biosensors because of its unique self-assembling behaviour. Studying its sequence-specific electronic properties is one such analysis that could be employed as a tool for understanding mechanisms of charge transfer for integration into DNA-based devices. Although known to be reasonably stable in aqueous solution, environmental factors can affect the helical structure, resulting in significantly attenuated electronic profile. DNA molecules are also not stable when stored for long periods in solution form at room temperature prompting many interests for solvents in which DNA structures exhibit long-term stability. Ionic liquid (IL), 1-butyl-3-methylimidazolium acetate ([BMIM][Ace]), is a potential solvent that ensures long-term stability of DNA. Therefore, in this work, the effect of IL on basidiomycetes DNAs integrated within an aluminium (Al)–indium tin oxide (ITO) Schottky junction was investigated. Significant improvement in the rectifying profiles was observed for DNA dissolved in [BMIM][Ace] (IL/DNA) compared to DNA in aqueous solution (aq/DNA) without the addition of IL when stored at different temperatures and time intervals. In general, the junction structure exhibited insulating behaviour when DNA was stored at room temperature for three months. This results in loss of its structure and stability for long periods of use at room temperature. Meanwhile, IL sample itself (control) shows a linear conductive profile. Furthermore, different solid-state parameters calculated allow us to understand the charge transfer mechanism in DNA molecules as a function of IL. [ABSTRACT FROM AUTHOR]

Feather keratin is a biomass generated in excess from various livestock industries. With appropriate processing, it holds potential as a green source for degradable biopolymer that could potentially replace current fossil fuel based materials. Several processing methods have been developed, but the use of ultrasonication has not been explored. In this study, we focus on (i) comparing and optimizing the dissolution process of turkey feather keratin through sonication and conventional processes, and (ii) generating a biodegradable polymer material, as a value added product, from the dissolved keratin that could be used in packaging and other applications. Sonication of feather keratin in pure ionic liquids (ILs) and a mixture containing ILs and different co-solvents was conducted under different applied acoustic power levels. It was found that ultrasonic irradiation significantly improved the rate of dissolution of feather keratin as compared to the conventional method, from about 2 h to less than 20 min. The amount of ILs needed was also reduced by introducing a suitable co-solvent. The keratin was then regenerated, analyzed and characterized using various methods. This material holds the potential to be reused in various appliances. [ABSTRACT FROM AUTHOR]

Coconut shell, a natural biopolymer, is available in high amounts as waste in many countries. It could potentially be a crucial renewable source of raw materials for the carbon fiber industry. In this study, a series of aprotic ionic liquids, [Bmim][Ace], [Bmim]Cl, [Emim][Ace], and [Emim]Cl, were used in the dissolution and regeneration process of coconut shell. The results indicate that the dissolution of coconut shell (up to 70 mg of coconut shell per g of solvent) can occur in aprotic ionic liquids under a nitrogen atmosphere at 110 °C (6 h) and 150 °C (2 h). The extraction efficiency was greatly influenced by temperature, time, particle size, and types of cations and anions in the ionic liquids. At 150 °C, 10% regenerated lignin was obtained in [Emim][Ace], which was higher compared with [Emim]Cl, [Bmim][Ace], and [Bmim]Cl. The recyclability of the ionic liquids during the dissolution process (up to four times) was also scrutinized. The structure and properties of the untreated coconut shell and regenerated lignin were characterized by Fourier transform infra-red (FTIR) spectroscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD) analysis, and proton nuclear magnetic resonance (1H NMR). [ABSTRACT FROM AUTHOR]

Wool keratin, a natural biopolymer, is potentially an important renewable source of raw materials for the polyamide plastics industry. Large quantities of non-spinnable and short fibers of wool are discarded globally and hence are available as low value waste materials. In this study, we have investigated different solvents, including ionic liquids and deep eutectic mixtures, for the dissolution and processing of wool. The results show that substantial dissolution of wool (up to 475 mg wool per gram of solvent) can be obtained in the 1-allyl-3-methylimidazolium dicyanamide [AMIM][dca] ionic liquid at 130 °C. Our studies also indicated enhanced dissolution (an additional 50-100 mg g-1) of wool upon the addition of a reducing agent to the ionic liquids. Water insoluble fractions (20-40%) were obtained on the addition of water to the dissolved wool. This regenerated fraction was characterized for structural and chemical changes and found to contain a larger fraction of β-sheets and random coils than the starting material. The water soluble fraction was characterised and the results indicated the presence of fragments of low molecular weight polypeptide chains. [ABSTRACT FROM AUTHOR]

Keratin from various livestock industries is currently a waste material that has potential as a source of polyamide polymers that could replace fossil fuel derived materials if processing methods can be developed. In this work we have investigated methods for the dissolution and regeneration of keratin. Dissolution of keratin (from turkey feather) in ionic liquids was conducted under nitrogen at 130 °C for 10 hours. It was found that [BMIM]Cl, [AMIM]Cl and [choline][thioglycolate] could dissolve turkey feather keratin without addition of solvent or other chemicals. A significant percentage of solubility was obtained, up to 45% by weight. A water insoluble fraction was recovered by addition of water to the solution (∼50%). The structure and properties of this regenerated, water insoluble fraction were investigated. Compared to the starting material, the regenerated keratin shows structural changes rather than chemical changes within the polypeptide chains. The remaining fraction, consisting of water soluble fragments, was characterised by gel electrophoresis. [ABSTRACT FROM AUTHOR]

• BAILs were used as a medium solvent to dissolve rice husk and depolymerize the lignin. • 78 % of regenerated lignin was effectively extracted from rice husk by [C 3 SO 3 HMIM]Cl. • Acidic properties of BAILs improve the delignification process. • [C 3 SO 3 HMIM][HSO 4 ] was successfully depolymerized the lignin into low molecular weight aromatic products. Lignocellulosic agricultural waste, like rice husk, is generated abundantly from rice milling industries. It is no longer mere waste but has become a treasure trove of outstanding potentials for sustainable environment growth. In this study, a series of Bronsted acidic ionic liquids (BAILs) were synthesized, characterized and used as a medium solvent to dissolve rice husk. Fractionation of rice husk into lignin, cellulose and hemicellulose was successfully achieved after 6 h of stirring at 100 °C. About 78 % and 53 % of the regenerated lignin were effectively extracted from rice husk by 1-methyl-3-(3-sulfopropyl)-imidazolium chloride, [C 3 SO 3 HMIM]Cl and 1-methyl-3-(3-sulfopropyl)-imidazolium acetate, [C 3 SO 3 HMIM][Ace] respectively, while 1-methyl-3-(3-sulfopropyl)-imidazolium hydrogen sulfate, [C 3 SO 3 HMIM][HSO 4 ] only extracted 11 % (based on the original rice husk). The regenerated lignin and cellulose were characterized using FTIR and TGA. Among the BAILs, [C 3 SO 3 HMIM]Cl was found to be a good medium solvent to extract lignin from rice husk and could be recycled up to four times. The regenerated lignin was further depolymerized using the synthesized BAILs at 120 °C (1 h) to generate low molecular weight aromatic products, which were analysed using gas chromatography-mass spectrometry (GC–MS). During depolymerization process, [C 3 SO 3 HMIM][HSO 4 ] was identified as an excellent solvent to depolymerize the lignin into low molecular weight aromatic products. [ABSTRACT FROM AUTHOR]