Central Glass and Ceramic Research Institute

Exhaled human breath analysis is a very promising field of research work having great potential for diagnosis of diseases in non-invasive way. Breath analysis has attracted huge attention in the field of medical diagnosis and disease monitoring in the last two decades. VOCs/gases (Volatile Organic Compounds) in exhaled breath bear the finger-prints of metabolic and biophysical processes going on in human body. It’s a non-invasive, fast, non-hazardous, cost effective, and point of care process for disease state monitoring and environmental exposure assessment in human beings. Some VOCs/gases in exhaled breath are bio-markers of different diseases and their presence in excess amount is indicative of un-healthiness. Breath analysis has the potential for early detection of diseases. However, it is still underused and commercial device is yet not available owing to multiferrious challenges. This review is intended to provide an overview of major biomarkers (VOCs/gases) present in exhaled breath, importance of their analysis towards disease monitoring, analytical techniques involved, promising materials for breath analysis etc. Finally, related challenges and limitations along with future scope will be touched upon.

Metal organic frameworks (MOFs) with diverse structural chemistry are being projected as futuristic electrode materials for Li-ion batteries. In this work, we report synthesis of Mn-1,3,5-benzenetricarboxylate MOF by a simple solvothermal method and its application as an anode material for the first time. Scanning electron microscopy of the synthesized MOF shows a bar shaped morphology where these bars, about 1 μm wide and of varied lengths between 2 and 20 μm, are made of porous sheets containing mesoporous walls and macroporous channels. The MOF anode, when examined in the potential window of 0.01-2.0 V versus Li/Li(+), shows high specific capacities of 694 and 400 mAh g(-1) at current densities of 0.1 and 1.0 A g(-1) along with good cyclability, retention of capacity, and sustenance of the MOF network. Ex situ X-ray diffraction, Fourier transform infrared, and X-ray photoelectron spectroscopy studies on the electrode material at different states of charge suggest that the usual conversion reaction for Li storage might not be applicable in this case. Conjugated carboxylates being weakly electron withdrawing ligands with a stronger π-π interaction, a probable alternative Li storage mechanism has been proposed that involves the organic moiety. The present results show promise for applying Mn-1,3,5-benzenetricarboxylate MOF as high performance <2 V anode.

Electrocatalytic oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) have attracted widespread attention because of their important role in the application of various energy storage and conversion devices, such as fuel cells, metal-air batteries and water splitting devices. However, the sluggish kinetics of the HER/OER/ORR and their dependency on expensive noble metal catalysts (e.g., Pt) obstruct their large-scale application. Hence, the development of efficient and robust bifunctional or trifunctional electrocatalysts in nanodimension for both oxygen reduction/evolution and hydrogen evolution reactions is highly desired and challenging for their commercialization in renewable energy technologies. This review describes some recent developments in the discovery of bifunctional or trifunctional nanostructured catalysts with improved performances for application in rechargeable metal-air batteries and fuel cells. The role of the electronic structure and surface redox chemistry of nanocatalysts in the improvement of their performance for the ORR/OER/HER under an alkaline medium is highlighted and the associated reaction mechanisms developed in the recent literature are also summarized.

A remarkably high saturation magnetization of ∼0.4μB∕Fe along with room temperature ferromagnetic hysteresis loop has been observed in nanoscale (4–40nm) multiferroic BiFeO3 which in bulk form exhibits weak magnetization (∼0.02μB∕Fe) and an antiferromagnetic order. The magnetic hysteresis loops exhibit exchange bias and vertical asymmetry which could be because of spin pinning at the boundaries between ferromagnetic and antiferromagnetic domains. Interestingly, both the calorimetric and dielectric permittivity data in nanoscale BiFeO3 exhibit characteristic features at the magnetic transition point. These features establish the formation of a true ferromagnetic-ferroelectric system with a coupling between the respective order parameters in nanoscale BiFeO3.

The present research describes a simple low‐temperature synthesis route of preparing bismuth ferrite nanopowders through soft chemical route using nitrates of Bismuth and Iron. Tartaric acid is used as a template material and nitric acid as an oxidizing agent. The synthesized powders are characterized by X‐ray diffractometry, thermogravimetry and differential thermal analysis, infrared spectroscopy, and scanning electron microscopy. The particle size of the powder lies between 3 and 16 nm. In the process, phase pure bismuth ferrite can be obtained at a temperature as low as 400°C, in contrast to 550°C for coprecipitation route. On the other hand, we find that, like solid state reaction route, Pechini's autocombustion method of synthesis generates a lot of impurity phases along with bismuth ferrite.

Frequency upconverted emissions centered at 526 and 547 nm from two thermodynamically coupled excited states of Er3+ doped in BaTiO3 nanocrystals were recorded in the temperature range from 322 to 466 K using a diode laser emitting at 980 nm as the excitation source. The ensemble measurements of the fluorescence intensity ratio (FIR) of the signals at 526 and 547 nm as a function of the temperature showed that the sensitivity (the rate in which the FIR changes with the temperature) of such sensor depends on the size of the nanocrystal. This is explained taking into consideration modifications of nonraditive relaxation mechanisms with the size of the nanocrystals.

MOF derived CeO2 showed a pseudocapacitance of 1204 F g(-1) at 0.2 A g(-1), far exceeding its theoretical capacitance (560 F g(-1)). The present study demonstrates that combination of a two-way strategy, controlled nano-architecture and redox active electrolyte additive, could potentially alleviate both low energy density and capacitance fading issues plaguing the current metal oxide pseudocapacitors.

Recently, there has been tremendous progress in the field of nanodimensional conducting polymers with the objective of tuning the intrinsic properties of the polymer and the potential to be efficient, biocompatible, inexpensive, and solution processable. Compared with bulk conducting polymers, conducting polymer nanostructures possess a high electrical conductivity, large surface area, short path length for ion transport and superior electrochemical activity which make them suitable for energy storage and conversion applications. The current status of polymer nanostructure fabrication and characterization is reviewed in detail. The present review includes syntheses, a deeper understanding of the principles underlying the electronic behavior of size and shape tunable polymer nanostructures, characterization tools and analysis of composites. Finally, a detailed discussion of their effectiveness and perspectives in energy storage and solar light harvesting is presented. In brief, a broad overview on the synthesis and possible applications of conducting polymer nanostructures in energy domains such as fuel cells, photocatalysis, supercapacitors and rechargeable batteries is described.

Molybdenum disulfide (MoS(2))-multiwalled carbon nanotube (MWCNT) hybrids have been prepared by simple dry grinding. Excellent initial charge capacity (1214 mA h g(-1)) and ~85% retention after 60 discharge-charge cycles at different current densities (100-500 mA g(-1)) make MoS(2)-MWCNT (1 : 1) hybrids a superior anode in Li-ion batteries.

We report here a facile and green synthetic approach to prepare magnetite (Fe(3)O(4)) nanoparticles (NPs) with magnetic core and polyethylene glycol (PEG) surface coating. The interaction of the bare and PEG-coated Fe(3)O(4) NPs with cytochrome c (cyt c, an important protein with direct role in the electron transfer chain) is also reported in this study. With ultrasonication as the only peptization method and water as the synthesis medium, this method is easy, fast, and environmentally benign. The PEG coated NPs are highly water dispersible and stable. The bare NPs have considerable magnetism at room temperature; surface modification by PEG has resulted in softening the magnetization. This approach can very well be applicable to prepare biocompatible, surface-modified soft magnetic materials, which may offer enormous utility in the field of biomedical research. Detailed characterizations including XRD, FTIR, TG/DTA, TEM, and VSM of the PEG-coated Fe(3)O(4) NPs were carried out in order to ensure the future applicability of this method. Although the interaction of bare NPs with cyt c shows reduction of the protein, efficient surface modification by PEG prevents its reduction.

The field of Tissue engineering and regenerative medicine that work towards creating functional tissue-constructs mimicking native tissue for repair and/or replacement of damaged tissues or whole organs have evolved rapidly over the past few decades. However, traditional tissue engineering approaches comprising of scaffolds, growth factors and cells showed limited success in fabrication of complex 3D shapes and in vivo organ regeneration leading to their non-feasibility for clinical applications from a logistical and economical viewpoint. In this regard, 3D bioprinting, which is an extended application of additive manufacturing is now being explored for tissue engineering and regenerative medicine as it involves the top-down approach of building the complex tissue in a layer by layer fashion, thereby producing precise geometries due to controlled nature of matter deposition with the help of anatomically accurate 3D models of the tissue generated by computer graphics. Here, we aim to provide a comprehensive review of the 3D bioprinting technology along with associated 3D bioprinting strategies including ink-jet printing, extrusion printing, stereolithography and laser assisted bioprinting techniques. We then focus on the applications of 3D bioprinting technology on construction of various representative tissue and oragans, including skin, cardiac, bone and cartilage etc. We further attempt to highlight the steps involved in each of those tissues/organs printing and discuss on the associated technological requirements based on the available reports from recent literature. We finally conclude with current challenges with 3D bioprinting technology along with potential solution for future technological advancement of efficient and cost-effective 3D bioprinting methods.

A regenerated optical fibre Bragg grating that survives temperature cycling up to 1,295°C is demonstrated. A model based on seeded crystallisation or amorphisation is proposed.

Polyvinylidene fluoride (PVDF) films are filled with various mass fractions (wt%) of hydrated metal salt (MgCl2·6H2O) (Mg-salt) to fabricate high performance piezoelectric energy harvesters (PEHs). They deliver up to 4 V of open circuit voltage by simply repeated human finger imparting (under a pressure of ∼4.45 kPa) and also generate sufficient power to turn on at least ten commercial blue light emitting diodes (LEDs) instantly. The enhanced piezo-response is attributed to the combined effect of the change in the inherent dipole moment of the electroactive phase containing PVDF itself and H-bonding arising between the Mg-salt filler and PVDF via electrostatic interactions. Furthermore, it also successfully charged the capacitors, signifying practical applicability as a piezoelectric based energy harvester power source. UV-visible optical absorption spectral analysis revealed the possibility to estimate a change in the optical band gap value at different concentrations of Mg-salt filler added PVDF films that possess a useful methodology where the Mg-salt can be used as an optical probe. In addition dielectric properties have been studied to understand the role of molecular kinetic and interfacial polarization occurs in H-bond PVDF films at different applied frequencies at room temperature.

Low electronic conductivity and slow faradic processes limit the performance of MnO2 as an electrochemical pseudocapacitor with respect to cycling and power density. Herein, we report preparation of single-phase α-MnO2, composed of an interconnected nanowire network with "cocoonlike" morphology, and its application as electrode in a symmetric aqueous supercapacitor. Increased "effective" surface area, coexistence of micropores and mesopores, and enhanced electron transport in these nanowire networks result in a specific pseudocapacitance (CS) of 775 F·g(-1) in 3 M KOH, derived from cyclic voltammetry in the potential window of -1 to +1 V at a scan rate of 2 mV·s(-1), the highest reported for two-electrode symmetric configuration. Furthermore, introduction of K4Fe(CN)6 as a redox-active additive to KOH results in ∼7 times increase in energy density at a power density of ∼6000 W·kg(-1). The presence of the Fe(CN)6(4-)/Fe(CN)6(3-) redox couple provides an electron buffer source compensating for the slow faradic reactions. The results demonstrate that this simple approach might be an effective way to enhance the redox kinetics and reversibility of transition metal oxide-based pseudocapacitors.

Er 3 + :Ag-antimony glass nanocomposites are synthesized in a new reducing glass (dielectric) matrix K2O–B2O3–Sb2O3 by a single-step melt-quench technique involving selective thermochemical reduction. The UV-vis-near-infrared absorption spectra show typical surface plasmon resonance (SPR) band of Ag0 nanoparticles (NPs) in addition to the distinctive absorption peaks of Er3+ ion. X-ray diffraction and selected area electron diffraction results indicate formation of Ag0 NPs along the (200) plane direction. The transmission electron microscopic image reveals the formation of spherical, fractal, and rod-shaped Ag0 NPs having maximum size ∼31 nm. The rod-shaped Ag0 NPs have aspect ratio ∼2.4. The field emission scanning electron microscopic image shows development of three dimensional cornlike microstructures. Photoluminescent upconversion under excitation at 798 nm exhibit two prominent emission bands of Er3+ ions centered at 536 (green) and 645 (red) nm due to S43/2→I415/2 and F49/2→I415/2 transitions, respectively. Both the bands undergo a maximum of three- and eightfold intensity enhancement, respectively, at Ag0 concentration of 0.007 wt % (1.8×1018 atoms/cm3). Local field enhancement induced by Ag0 SPR is found to be responsible for enhancement while energy transfer from Er3+→Ag0 and optical reabsorption due to Ag0 SPR for quenching.

Pure hydroxyapatite (HAp) and a biphasic calcium phosphate [containing 90% of beta-tri-calcium phosphate (beta-TCP) and 10% HAp] were tailored through an aqueous solution combustion synthesis. Porous struts were prepared using all the powders along with bioglass, a known bioactive material, and subsequently characterized. Sterilized struts were implanted to the lateral side of radius bone of 24 black Bengal goats of either sex, in which a blank hole was left unfilled in a group of six specimens to act as control. The bone formation response of the three implanting materials in vivo has been studied using scanning electron microscope and histological analysis in contrast with positive controls. Push-out tests were used to assess the mechanical strength at the bone-biomaterial interface. It was observed that interfacial response was strongly dependent on combinations of different physical and chemical parameters. The surface of beta-TCP exhibited similar characteristics of bone and was distinct from those of intervening apatite layer of bioglass. Lower bone ingrowth and reduced strength was observed with HAp compared to beta-TCP/bioglass-based implants. Bone formation response of the Ca-P material varied according to the composition of the implanting material, which could be tailored through this novel synthesis.

Oak has been converted to a porous biocarbon template by annealing in an inert atmosphere above 800°C. Subsequent infiltration with gaseous SiO at 1550–1600°C under flowing argon of atmospheric pressure finally resulted in the formation of a porous, cellular β‐SiC ceramic. The conversion retains the biomorphic cellular morphology of oak tissue. While pores in the cell walls with a diameter less than ∼1 μm vanished, two distinct pore channel maxima representing tracheidal cells and large vessels remained in the SiC ceramic. Depending on the cellular morphology of different kinds of wood, e.g., strut thickness and pore size distribution, gas‐phase conversion to single‐phase β‐SiC can be used to manufacture cellular ceramics with a wide range of pore channel diameters.

Nanocomposites of poly(vinyl alcohol) (PVA), poly(vinyl pyrrolidone) (PVP) and sodium montmorillonite (Na+MMT) were prepared by solution mixing and then cast into films. X-ray diffraction analysis and images of transmission electron microscopy establish the formation of PVA/Na+MMT intercalated nanocomposite. Exfoliated and highly intercalated PVA/PVP/Na+MMT nanocomposite formed in the presence of PVP. Inclusion of PVP in PVA/Na+MMT matrix enhances the hydrogen bonding interactions between PVA and Na+MMT and thus increases the mechanical properties and thermal stability of PVA/PVP/Na+MMT nanocomposites compared to PVA/Na+MMT nanocomposite. The interactions between PVA, PVP and Na+MMT were established by the Fourier transform infrared spectroscopy. The moisture absorption tendency of both the PVA and PVA/PVP films reduced after the incorporation of Na+MMT at 75% constant relative humidity. Differential scanning calorimetry studies show that the presence of PVP and Na+MMT both are responsible for reducing the heat of fusion, and crystallinity of PVA. The flow behavior of the PVA, PVA/PVP and its nanocomposite solutions has been also studied. Water vapor permeability of PVA/PVP/Na+MMT composite films decreased in the presence of nanoclay due to increasing tortuous paths for diffusion.

Inherent properties of graphene can be experienced by integrating it with different nanomaterials to form unique composite materials. Decorating the surface of graphene sheets with nanoparticles (NPs) is one of the recent approaches taken up by scientists all over the world. This article describes a simple synthesis route to preparing stable Ni NP-reduced graphene oxide (Ni-RGO) composite material. The otherwise unstable bare Ni NPs are stabilized when embedded in the RGO sheets. This synthesized composite material has a potential application in the formic acid-induced reduction of highly toxic aqueous Cr(VI) at room temperature (25 °C). The reduction of dichromate using formic acid as a reducing agent is a well-known redox reaction. However, the rate of the reaction is very slow at room temperature, which can be enhanced very significantly in the presence of Ni-RGO by introducing an intermediate redox step with formic acid. The Ni-RGO composite material is an easy to prepare, cheap, stable, reusable material that has the potential to replace costly Pd NPs used in this context. Ni-RGO is also found to be very active in enhancing the rate of reduction of other metal ions in the presence of formic acid at room temperature.

The kaolinite‐to‐mullite reaction series was reexamined with special attention to the nature of the metaphase, the eontroversial spinel phase, and the cause of the exothermic peak at 980°C. Amorphous SiO 2 forms during the exothermic reaction; it can be leached by alkali extraction. When the residual cubic phase is heated further, it forms mullite only. This result indicates that the cubic phase is an Al‐Si spinel and that metakaolinite is an AI 2 O 3 ‐SiO 2 compound. It was established that the exotherm exhibited by kaolinite at 980°C represents the sudden transformation of metakaolinite to Al‐Si spinel, the crystallization of mullite, and the liberation of amorphous SiO 2 . The AI‐Si spinel has the same composition as mullite, containing both AI(IV) and AI(VI). This spinel transforms into mullite at the second exothermic peak; no amorphous SiO 2 is liberated.