Search

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.

Imbuing superwetting functions to organic-inorganic hybrid networks displaying chemical resistance, self-cleaning ability, and selective permeation of liquids has received increasing attention in recent years. Here we report superhydrophobic ZIF-7 and ZIF-11 on multilayer fluorinated graphene (FG) nanosheets with long-lasting water-repellent features. By exploring the solution processing of these chemically resistant dispersions, superoleophilic FG-ZIF-7 stainless steel mesh (FG-ZIF-7-SSM) and FG-ZIF-11 over cotton cloth (FG-ZIF-11-CC) possessing superior adhesion were fabricated. These permselective oil-liking prototypes were explored toward mesitylene and crude oil pickup from chemically harsh marine conditions such as seawater, acidic water, and alkaline water, with a separation efficiency of 96-94% up to 10 cycles. Furthermore, using an FG-ZIF-11-CC-wrapped glass pipet, upward diffusion of chloroform from sea, acidic, and alkaline water in 45 s was demonstrated with a separation efficacy of 94% up to 20 cycles. In addition to the chemical resistance and reusability, the mechanical stability of FG-ZIF-7-SSM and FG-ZIF-11-CC was investigated through folding, tape peeling, and dragging through sandpaper up to 250 cycles, showing no signs of changes in the hydrophobic responses. This research sheds light on the application of physiochemically resistant percolation coatings based on fluorinated graphene multilayers supporting ZIF-7 and ZIF-11 toward oil/water separation.

The recent trend in thermoelectric literature suggests that ionic thermoelectric (i-TE) materials are ideal for directly converting low-grade waste heat into electricity. Here, we developed a unique platform for i-TE studies by stacking two-dimensional sheets of β-Ni(OH) 2 prepared by a bottom-up method. The lamellar membrane of β-Ni(OH) 2 (Ni-M) itself does not display significant thermovoltages, but when doped with mobile anion-generating species (like aminopropyl functionalized magnesium phyllosilicate or organic halide salts), it exhibits significant negative Seebeck coefficient (up to -13.7 ± 0.2 mV K -1 ). Similarly, upon doping with cation-generating species like poly(4-styrene sulfonic acid) (PSS), it displays positive Seebeck coefficient values (up to +12 ± 1.9 mV K -1 ). The positive and negative i-TE materials prepared by doping Ni-M are assembled into ionic thermopiles capable of generating thermovoltages up to 1 V, at Δ T = 12 K. The Ni-M-based nanofluidic systems demonstrated an additional path of electricity harvesting by connecting colder zones of the positive and negative i-TE materials with other ion conducting membranes. In contrast to organic polymer-based i-TE systems, the Ni-M based system exhibited consistent performance despite being exposed to high temperatures (∼200 °C, 5 minutes).

Silver-based electrocatalysts as promising substitutes for platinum materials for cathodic oxygen electroreduction have been extensively researched. Electrocatalytic enhancement of the Ag nanoarchitectonics can be obtained via support structures and amalgamating Ag with one or two additional metals. The work presented here deals with a facile microwave-assisted synthesis to produce bimetallic Ag-Cu and Ag-Co (1:1) oxide nanoparticles (NPs) and trimetallic AgCuCo (0.6:1.5:1.5, 2:1:1, and 6:1:1) oxide NPs supported on a reduced graphene oxide (rGO) matrix. Morphology, composition, and functional groups were methodically analysed using various microscopic and spectroscopic techniques. The as-prepared electrocatalysts were employed as cathode substrates for the oxygen reduction reaction (ORR) in alkaline medium. Varying the Ag fraction in copper cobalt oxide has a significant influence on the ORR activity. At a ratio of 2:1:1, AgCuCo oxide NPs on rGO displayed the best values for onset potential, half-wave potential, and limiting current density ( J k ) of 0.94 V vs RHE, 0.78 V, and 3.6 mA·cm -2 , respectively, with an electrochemical active surface area of 66.92 m 2 ·g -1 and a mass activity of 40.55 mA·mg -1 . The optimum electrocatalyst shows considerable electrochemical stability over 10,000 cycles in 0.1 M KOH solution., (Copyright © 2022, Madakannu et al.)

Designing hydrophobic-oleophilic sorbent materials have gained significant interest owing to its potential applications in self-cleaning technologies particularly oil-water separation. The crucial factors remain in the future research of designing materials with high performance hydrophobicoleophilic properties include facile synthesis, low-density, reusability and ecofriendly. Herein, we develop porous hydrophobic-oleophilic nanoarchitecture based on 2D fluorinated graphene (FG) supported cobalt based zeolite imidazole framework (ZIF-67) by solution assisted self-assembly. The key features of the work include in-situ growth and assembly of ZIF-67 over functionalized fluorinated graphene f -FG macrostructures, high surface area and solution processable and spray coated sponge. Methodical characterization of f -FG@ZIF-67 composites, followed by measuring water contact angles by contact angle goniometer. Furthermore, the assessment of sorption capacity of oils and organics followed by oil recovery from oil-water mixtures, excellent chemical and physical stabilities were displayed by these hydrophobic-oleophilic composites.

We report a facile methodology for the synthesis of inorganic-organic hydrogels based on integrative assembly of aminopropyl magnesium phyllosilicate (aminoclay) and sodium salt of hyaluronic acid. The viscoelastic materials produced by electrostatic interactions and crosslinking of hyaluronan in the presence of exfoliated synthetic organoclay results in the formation of gel-like behavior retaining a high amount of water. This was confirmed by a rheological study revealing significant dominance of the elastic response over the entire deformation frequency range used. The mechanical strength of the aminoclay-hyaluronan hydrogels was found to be higher than that for related materials based on poly(vinylpyrrolidone)-aminoclay hydrogels., (Copyright © 2018 Elsevier B.V. All rights reserved.)

The design of advanced high-energy-density supercapacitors requires the design of unique materials that combine hierarchical nanoporous structures with high surface area to facilitate ion transport and excellent electrolyte permeability. Here, shape-controlled 2D nanoporous carbon sheets (NPSs) with graphitic wall structure through the pyrolysis of metal-organic frameworks (MOFs) are developed. As a proof-of-concept application, the obtained NPSs are used as the electrode material for a supercapacitor. The carbon-sheet-based symmetric cell shows an ultrahigh Brunauer-Emmett-Teller (BET)-area-normalized capacitance of 21.4 µF cm -2 (233 F g -1 ), exceeding other carbon-based supercapacitors. The addition of potassium iodide as redox-active species in a sulfuric acid (supporting electrolyte) leads to the ground-breaking enhancement in the energy density up to 90 Wh kg -1 , which is higher than commercial aqueous rechargeable batteries, maintaining its superior power density. Thus, the new material provides a double profits strategy such as battery-level energy and capacitor-level power density., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)