Graphene’s unique physical structure, as well as its chemical and electrical properties, make it ideal for use in sensor technologies. In the past years, novel sensing platforms have been proposed with pristine and modified graphene with nanoparticles and polymers. Several of these platforms were used to immobilize biomolecules, such as antibodies, DNA, and enzymes to create highly sensitive and selective biosensors. Strategies to attach these biomolecules onto the surface of graphene have been employed based on its chemical composition. These methods include covalent bonding, such as the coupling of the biomolecules via the 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and N-hydroxysuccinimide reactions, and physisorption. In the literature, several detection methods are employed; however, the most common is electrochemical. The main reason for researchers to use this detection approach is because this method is simple, rapid and presents good sensitivity. These biosensors can be particularly useful in life sciences and medicine since in clinical practice, biosensors with high sensitivity and specificity can significantly enhance patient care, early diagnosis of diseases and pathogen detection. In this review, we will present the research conducted with antibodies, DNA molecules and, enzymes to develop biosensors that use graphene and its derivatives as scaffolds to produce effective biosensors able to detect and identify a variety of diseases, pathogens, and biomolecules linked to diseases.

was also confirmed by XPS (Fig. 2), and explained by the reactions in Eqs. (7) and (8). Furthermore, the peak of the C-H stretching at 2848 cm −1 became less visible in the used CS-PEI-GO due to the oxidation of the C-H of the chitosan (Eq. 9). When the C-H functional group was oxidized, the hydroxyl band observed in the ATR-FTIR (Figure S4) spectra became more intense.

Increasing human activity, including commercial and noncommercial use of pharmaceuticals, personal care products, and agricultural products, has introduced new contaminants that can be challenging to remove with currently available technologies. Pharmaceuticals, in particular, can be especially challenging to remove from the water supply and can pose great harm to people and local ecosystems. Their highly stable nature makes their degradation with conventional water treatment techniques difficult, and studies have shown that even advanced treatment of water is unable to remove some compounds. As such, decontamination of water from pharmaceuticals requires the development of advanced technologies capable of being used in indirect and direct potable water reuse. In this review, we discuss pharmaceutical removal in indirect potable water treatment and how recent advancements in adsorption and photocatalysis technologies can be used for the decontamination of pharmaceutical-based emerging contaminants. For instance, new materials that incorporate graphene-based nanomaterials have been developed and shown to have increased adsorptive capabilities toward pharmaceuticals when compared with unmodified graphene. In addition, adsorbents have been incorporated in membrane technologies, and photocatalysts have been combined with magnetic material and coated on optical fibers improving their usability in water treatment. Advancements in photocatalytic material research have enabled the development of highly effective materials capable of degradation of a variety of pharmaceutical compounds and the development of visible-light photocatalysts. To understand how adsorbents and photocatalysts can be utilized in water treatment, we address the benefits and limitations associated with these technologies and their potential applicability in indirect potable water reuse plants.

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The present study reports two routes to modify reduced graphene oxide (rGO) nanosheets with polysulfone (PSU) brushes via nitrene chemistry. The PSU polymer is bonded to rGO at the extremity (rGO-PSU end) and at the middle of the PSU chain (rGO-PSU mid). The resulting rGO-PSU synthetic products are carefully characterized by Raman and FTIR spectroscopy, XPS, TEM, and thermogravimetric analysis, evidencing the successful grafting of PSU onto rGO surfaces. The long-term stability of these nanosheets is also determined in common solvents. The antibacterial properties of polymer-functionalized rGO against the planktonic Bacilus subtilis and Escherichia coli are also investigated. It is established that the antimicrobial properties of these nanocomposites are due to the production of reactive oxygen species. The results also demonstrate that rGO-PSU mid presents better antimicrobial properties due to shorter polymer chains, which improves the contact of the microorganisms with the graphene surface.

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The chemical synthesis of monoatomic metallic copper is unfavorable and requires inert or reductive conditions and the use of toxic reagents. Here, we report the environmental extraction and conversion of CuSO4 ions into single-atom zero-valent copper (Cu0) by a copper-resistant bacterium isolated from a copper mine in Brazil. Furthermore, the biosynthetic mechanism of Cu0 production is proposed via proteomics analysis. This microbial conversion is carried out naturally under aerobic conditions eliminating toxic solvents. One of the most advanced commercially available transmission electron microscopy systems on the market (NeoArm) was used to demonstrate the abundant intracellular synthesis of single-atom zero-valent copper by this bacterium. This finding shows that microbes in acid mine drainages can naturally extract metal ions, such as copper, and transform them into a valuable commodity.