Polymer Waste Valorization into Advanced Carbon Nanomaterials for Potential Energy and Environment Applications.

The rise in universal population and accompanying demands have directed toward an exponential surge in the generation of polymeric waste. The estimate predicts that world-wide plastic production will rise to ≈590 million metric tons by 2050, whereas 5000 million more tires will be routinely abandoned by 2030. Handling this waste and its detrimental consequences on the Earth's ecosystem and human health presents a significant challenge. Converting the wastes into carbon-based functional materials viz. activated carbon, graphene, and nanotubes is considered the most scientific and adaptable method. Herein, this world provides an overview of the various sources of polymeric wastes, modes of build-up, impact on the environment, and management approaches. Update on advances and novel modifications made in methodologies for converting diverse types of polymeric wastes into carbon nanomaterials over the last 5 years are given. A remarkable focus is made to comprehend the applications of polymeric waste-derived carbon nanomaterials (PWDCNMs) in the CO2 capture, removal of heavy metal ions, supercapacitor-based energy storage and water splitting with an emphasis on the correlation between PWDCNMs' properties and their performances. This review offers insights into emerging developments in the upcycling of polymeric wastes and their applications in environment and energy.

Hierarchical Porous Activated Carbon from Wheat Bran Agro-Waste: Applications in Carbon Dioxide Capture, Dye Removal, Oxygen and Hydrogen Evolution Reactions.

This work reports an efficient method for facile synthesis of hierarchically porous carbon (WB-AC) utilizing wheat bran waste. Obtained carbon showed 2.47 mmol g-1 CO2 capture capacity with good CO2 /N2 selectivity and 27.35 to 29.90 kJ mol-1 isosteric heat of adsorption. Rapid removal of MO dye was observed with a capacity of ~555 mg g-1 . Moreover, WB-AC demonstrated a good OER activity with 0.35 V low overpotential at 5 mA cm-2 and a Tafel slope of 115 mV dec-1 . It also exhibited high electrocatalytic HER activity with 57 mV overpotential at 10 mA cm-2 and a Tafel slope of 82.6 mV dec-1 . The large SSA (757 m2 g-1 ) and total pore volume (0.3696 cm3 g-1 ) result from N2 activation contributing to selective CO2 uptake, high and rapid dye removal capacity and superior electrochemical activity (OER/HER), suggesting the use of WB-AC as cost effective adsorbent and metal free electrocatalyst.

Rational La-doped hematite as an anode and hydrous cobalt phosphate as a battery-type electrode for a hybrid supercapacitor.

In recent years, modern appliances require high energy density with a burst power supply. Hybrid supercapacitors show high performance based on high energy density without compromising power density and stability over thousands of charge-discharge cycles. In this work, the optimized hybrid electrodes using lanthanum-doped hematite (lanthanum-doped iron oxide) noted as 7.5%La-HMT as a negative electrode and hydrous cobalt phosphate (CoPO) as a battery-type positive electrode have been successfully fabricated via a simple hydrothermal method and a facile co-precipitation method, respectively. The 7.5%La-HMT showed excellent electrochemical performance due to doping of rare-earth La3+ metal ions, resulting in improvised active sites and reduction in the equivalent resistance. The 7.5%La-HMT operated at a high potential window (0 to -1.2 V) with an ultra-high specific capacitance (Sp) of 1226.7 F g-1 at 1 A g-1 with capacitance retention of 89.3% over 1000 cycles. CoPO could be operated at a high working window (0 to 0.45 V) with a specific capacity of 121.7 mA h g-1 at a current density of 2 A g-1 with capacitance retention of 85.4% over 1000 cycles. The configured CoPO//KOH//10%La-HMT aqueous hybrid capacitor device (Aq-HSC) could be operated at a potential window of 1.6 V and delivered a maximum energy density (E.D) of 83.6 W h kg-1 at a power density (P.D) of 3.2 kW kg-1 with Sp of 235.0 F g-1 at 2 A g-1 and 89.0% Sp retention over 5000 cycles. The simplicity of the synthesis methods for CoPO and 7.5%La-HMT along with their superior super-capacitive properties make them suitable for advanced electrical devices and hybrid vehicles.

The implementation of graphene-based aerogel in the field of supercapacitor.

Graphene and graphene-based hybrid materials have emerged as an outstanding supercapacitor electrode material primarily because of their excellent surface area, high electrical conductivity, and improved thermal, mechanical, electrochemical cycling stabilities. Graphene alone exhibits electric double layer capacitance (EDLC) with low energy density and high power density. The use of aerogels in a supercapacitor is a pragmatic approach due to its extraordinary properties like ultra-lightweight, high porosity and specific surface area. The aerogels encompass a high volume of pores which leads to easy soak by the electrolyte and fast charge-discharge process. Graphene aerogels assembled into three-dimensional (3D) architecture prevent there stacking of graphene sheets and maintain the high surface area and hence excellent cycling stability and rate capacitance. However, the energy density of graphene aerogels is limited due to EDLC type of charge storage mechanism. Consequently, 3D graphene aerogel coupled with pseudocapacitive materials such as transition metal oxides, metal hydroxides, conducting polymers, nitrides, chalcogenides show an efficient energy density and power density performance due to the presence of both types of charge storage mechanisms. This laconic review focuses on the design and development of graphene-based aerogel in the field of the supercapacitor. This review is an erudite article about methods, technology and electrochemical properties of graphene aerogel.

Understanding Time Dependence on Zinc Metal-Organic Framework Growth Using in Situ Liquid Secondary Ion Mass Spectrometry.

The abundance of novel metal-organic framework (MOF) materials continues to increase as more applications are discovered for these highly porous, well-ordered crystalline structures. The simplicity of constituents allows for the design of new MOFs with virtue of functionality and pore topology toward target adsorbates. However, the fundamental understanding of how these frameworks evolve during nucleation and growth is mostly limited to speculation from simulation studies. In this effort, we utilize a unique vacuum compatible system for analysis at the liquid vacuum interface (SALVI) microfluidic interface to analyze the formation and evolution of the benchmark MOF-74 framework using time-of-flight secondary ion mass spectrometry (ToF-SIMS). Principal component analysis of the SIMS mass spectra, together with ex situ electron microscopy, powder X-ray diffractometry, and porosimetry, provides new insights into the structural growth, metal-oxide cluster formation, and aging process of Zn-MOF-74. Samples collected over a range of synthesis times and analyzed closely with in situ ToF-SIMS, transmission electron microscopy, and gas adsorption studies verify the developing pore structure during the aging process.

Rational design of coumarin derivatives as antituberculosis agents.

AIM: A series of coumarin derivatives was designed as potential antituberculosis agents. RESULTS: The compounds were screened against active and dormant Mycobacterium tuberculosis (Mtb). Compounds 3k and 3n were found to have the most promising activity against replicating MtbH37Rv exhibiting minimum inhibitory concentration of 4.63 and 9.75 µM respectively. The compounds were also effective against dormant MtbH37Rv exhibiting more potency than the standard drugs, isoniazid and rifampicin. The compounds were found to be non-cytotoxic against human cell lines. CONCLUSION: This study provides promising antituberculosis agents that are effective against replicating as well as dormant Mtb and can thus act as potential leads for further development.

Recent developments in the synthesis, properties, and biomedical applications of core/shell superparamagnetic iron oxide nanoparticles with gold.

In the last decade, magnetic nanoparticles (MNPs), especially superparamagnetic iron oxide nanoparticles (SPIONs), have immensely promoted the advancement of diagnostics and theranostics in the biomedical field. The unique properties of the SPIONs-core and the functional gold (Au)-shell together (SPIONS/Au core/shell or CS) have a wide range of biomedical applications including, but not limited to, magnetic resonance imaging (MRI), dual modality MRI/computed tomography (CT), photo-induced and magnetic fluid hyperthermia (MFH), drug delivery, biosensors, and bio-separation. Researchers have made much effort to develop synthesis strategies for size control and surface modifications to achieve the desired properties of these CSs for applications in in vitro and in vivo studies. This review highlights recent developments in the synthesis and biomedical applications of SPIONs/Au CSs, including γ-Fe2O3/Au (maghemite), Fe3O4/Au (magnetite), and MFe2O4/Au (M = divalent metal ions) in the past seven years. More importantly, current trends of SPIONs/Au in relation to the biochemical industry are surveyed. Finally, we outline the developmental needs of SPIONs/Au from the perspective of material synthesis and their novel applications in disease diagnosis and treatment in the near future.

Superparamagnetic MFe2O 4 (M = Ni, Co, Zn, Mn) nanoparticles: synthesis, characterization, induction heating and cell viability studies for cancer hyperthermia applications.

Superparamagnetic nanoferrites are prepared by simple and one step refluxing in polyol synthesis. The ferrite nanoparticles prepared by this method exhibit particle sizes below 10 nm and high degree of crystallinity. These ferrite nanoparticles are compared by means of their magnetic properties, induction heating and cell viability studies for its application in magnetic fluid hyperthermia. Out of all studied nanoparticles in present work, only ZnFe2O4 and CoFe2O4 MNPs are able to produce threshold hyperthermia temperature. This rise in temperature is discussed in detail in view of their magneto-structural properties. Therefore ZnFe2O4 and CoFe2O4 MNPs with improved stability, magnetic induction heating and cell viability are suitable candidates for magnetic hyperthermia.

Lake contamination by accumulation of heavy metal ions in Eichhornia crassipes: a case study of Rankala Lake, Kolhapur (India).

The absorption of heavy metals into biomaterial derived from the plant Eichhornia crassipes was investigated. The root, stem and leaf samples of the plant collected from the Rankala Lake of Kolhapur city (India) were analyzed for the metal ion concentrations using Atomic Absorption Spectrometer. It has been observed that in root, stem and leaf, Pb ions get absorbed, while the extent of absorption for each element found different in the parts analyzed. In root, the order for metal ion absorption found to be Fe>Mn>Cu>Zn>Cr>Pb>Ni>Co>Cd ions. Thus, it is clear that Eichhornia crassipes absorbs heavy metal ions and can be used for minimizing the pollution taking place due to toxic metal ions in the effluents from various industries.

Chromatographic separation of cerium(III) in L-valine medium using poly[dibenzo-18-crown-6].

A column chromatographic method has been developed for the separation and determination of cerium(III) using poly[ dibenzo-18-crown-6]. The separation was carried out in L-valine medium. The adsorption of cerium(III) was quantitative from 1 x 10(-1) to 1 x 10(-4) mol/L L-valine. Amongst the various elements, 1.0-8.0 mol/L hydrochloric acid, 1.0-8.0 mol/L hydrobromic acid, 1.0-8.0 mol/L perchloric acid, 1.0-2.0 mol/L sulfuric acid and 4.0-5.0 mol/L acetic acid, were found to be the efficient eluents for cerium(III). The capacity of poly[ dibenzo-18-crown-6] for cerium(III) was (0.428 +/- 0.01) mmol/g. The method was applied to the separation of cerium(III) from associated elements link uranium(VI) and thorium(IV). It was also applied for the determination of cerium(III) in geological samples. The method is simple, rapid and selective with good reproducibility (approximately +/-2%).