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Porous carbon materials from food waste have gained growing interest worldwide for multiple applications due to their natural abundance and the sustainability of the raw materials and the cost-effective synthetic processing. Herein, orange waste-derived porous carbon (OWPC) was developed through a freeze-drying method to prevent the demolition of the original biomass structure and then was pyrolyzed to create a large number of micro, meso and macro pores. The novelty of this work lies in the fact of using the macro-channels of the orange waste in order to create a macroporous network via the freeze-drying method which remains after the pyrolysis steps and creates space for the development of different types of porous in the micro and meso scale in a controlled way. The results showed the successful preparation of a porous carbon material with a high specific surface area of 644 m 2 g -1 without any physical or chemical activation. The material's cytocompatibility was also investigated against a fibroblast cell line (NIH/3T3 cells). OWPC triggered a mild intracellular reactive oxygen species production without initiating apoptosis or severely affecting cell proliferation and survival. The combination of their physicochemical characteristics and high cytocompatibility renders them promising materials for further use in biomedical and pharmaceutical applications.

Cationic quaternized carbon dots (QCDs) and anionic graphene oxide sheets (GO) are combined via non-covalent interactions following a self-assembly pathway to form highly biocompatible and fluorescent hybrid materials. These hybrids act as selective probes with controlled labelling of the cell nucleus or cytoplasm depending on the QCD loading.

In this research, we report the binding behaviors of two kinds of intercalators, methyl violet and 3,6-diaminoacridine hydrochloride, to various mesoporous materials, carbon nanocage, mesoporous carbon CMK-3, activated carbon, and mesoporous silica SBA-15. Due to its unique cage type structure, carbon nanocage shows greater adsorption capacity than the other adsorbents. In addition, competitive adsorption of methyl violet between DNA and mesoporous materials confirmed that carbon nanocage can very efficiently inhibit intercalation of methyl violet by DNA. Carbon nanocage might then be useful for entrapment of harmful aromatic molecules.

The use of two-dimensional templates like clay, in the synthesis of graphitic carbon nitrides, make it feasible to form exfoliated layer like structures by polymerization of the precursors in the clay galleries. We have used clay linked with aminopropyl groups, aminoclay, to template the carbon nitride into mesolamellar structures. By virtue of its aminopropyl groups, aminoclay is further capable of reacting along with the intercalated precursors to enrich the carbon content of the resulting carbon nitrides. [ABSTRACT FROM AUTHOR]