We report a systematic evaluation of the use of refluxing nitric acid as a purification treatment for electric
arc-produced single-walled carbon nanotubes (SWNTs), by using a combination of thermogravimetric analysis
(TGA) and near-infrared (NIR) spectroscopy. Nitric acid is the standard reagent for purification of SWNTs
and has traditionally constituted the first step in many different purification schemes. It has been suggested
that nitric acid removes the transition metal catalyst that is used in the production of the SWNTs together
with amorphous carbon. Under all conditions, we find that nitric acid destroys SWNTs to produce amorphous
carbon while reducing the amount of transition metal catalyst remaining in the sample. Thus, nitric acid is
suitable for removing the catalyst from SWNT samples, but only at the expense of a significant destruction
of the SWNTs.
Two-dimensional covalent organic frameworks (2D COFs) provide a unique platform for the molecular design of electronic and optoelectronic materials. Here, the synthesis and characterization of an electroactive COF containing the well-known tetrathiafulvalene (TTF) unit is reported. The TTF-COF crystallizes into 2D sheets with an eclipsed AA stacking motif, and shows high thermal stability and permanent porosity. The presence of TTF units endows the TTF-COF with electron-donating ability, which is characterized by cyclic voltammetry. In addition, the open frameworks of TTF-COF are amenable to doping with electron acceptors (e.g., iodine), and the conductivity of TTF-COF bulk samples can be improved by doping. Our results open up a reliable route for the preparation of well-ordered conjugated TTF polymers, which hold great potential for applications in fields from molecular electronics to energy storage.
β-glucan is a type of polysaccharide which widely exists in bacteria, fungi, algae, and plants, and has been well known for its biological activities such as enhancing immunity, antitumor, antibacterial, antiviral, and wound healing activities. The conformation of β-glucan plays a crucial role on its biological activities. Therefore, β-glucans obtained from different sources, while sharing the same basic structures, often show different bioactivities. The basic structure and inter-molecular forces of polysaccharides can be changed by modification, which leads to the conformational transformation in solution that can directly affect bioactivity. In this review, we will first determine different ways to modify β-glucan molecules including physical methods, chemical methods, and biological methods, and then reveal the relationship of the flexible helix form of the molecule chain and the helix conformation to their bioactivities. Last, we summarize the scientific challenges to modifying β-glucan’s conformation and functional activity, and discuss its potential future development.
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