Institute of Chemical Technology

The concept of resistant starch (RS) has evoked new interest in the bioavailability of starch and in its use as a source of dietary fiber, particularly in adults. RS is now considered to provide functional properties and find applications in a variety of foods. Types of RS, factors influencing their formation, consequence of such formation, their methods of preparation, their methods of estimation, and health benefits have been briefly discussed in this review.

The coordinatively unsaturated sites in MIL-101, Cr3(F,OH)(H2O)2O[(O2C)-C6H4-(CO2)]3⋅n H2O (n≈25), having zeotypic giant pores can be selectively functionalized in a way differing from that of mesoporous silica. Metal–organic frameworks, grafted with ethylenediamine or diethylenetriamine on the unsaturated CrIII sites of MIL-101, exhibit remarkably high activities in the Knoevenagel condensation relative to that of the mesophase.

Nanosuspensions have emerged as a promising strategy for the efficient delivery of hydrophobic drugs because of their versatile features and unique advantages. Techniques such as media milling and high-pressure homogenization have been used commercially for producing nanosuspensions. Recently, the engineering of nanosuspensions employing emulsions and microemulsions as templates has been addressed in the literature. The unique features of nanosuspensions have enabled their use in various dosage forms, including specialized delivery systems such as mucoadhesive hydrogels. Rapid strides have been made in the delivery of nanosuspensions by parenteral, peroral, ocular and pulmonary routes. Currently, efforts are being directed to extending their applications in site-specific drug delivery.

Pharmaceutical compounds are typically produced in batch processes leading to the presence of a wide variety of products in wastewaters which are generated in different operations, wherein copious quantities of water are used for washing of solid cake, or extraction, or washing of equipment. The presence of pharmaceutical compounds in drinking water comes from two different sources: production processes of the pharmaceutical industry and common use of pharmaceutical compounds resulting in their presence in urban and farm wastewaters. The wastewaters generated in different processes in the manufacture of pharmaceuticals and drugs contain a wide variety of compounds. Further, reuse of water after removal of contaminants, whether pharmaceuticals or otherwise, is required by industry. In view of the scarcity of water resources, it is necessary to understand and develop methodologies for treatment of pharmaceutical wastewater as part of water management. In this review, the various sources of wastewaters in the pharmaceutical industry are identified and the best available technologies to remove them are critically evaluated. Effluent arising from different sectors of active pharmaceutical ingredients (API), bulk drugs, and related pharmaceutics, which use large quantities of water, is evaluated and strategies are proposed to recover to a large extent the valuable compounds, and finally the treatment of very dilute but detrimental wastewaters is discussed. No single technology can completely remove pharmaceuticals from wastewaters. The use of conventional treatment methods along with membrane reactors and advanced posttreatment methods resulting in a hybrid wastewater treatment technology appear to be the best. The recommendations provided in this analysis will prove useful for treatment of wastewater from the pharmaceutical industry.

The formation of gas bubbles and their subsequent rise due to buoyancy are very important fundamental phenomena that contribute significantly to the hydrodynamics in gas−liquid reactors. The rise of a bubble in dispersion can be associated with possible coalescence and dispersion followed by its disengagement from the system. The phenomenon of bubble formation decides the primitive bubble size in the system (which latter attains an equilibrium size), whereas the rise velocity decides the characteristic contact time between the phases which governs the interfacial transport phenomena as well as mixing. In view of their importance, we herein present a comprehensive review of bubble formation and bubble rise velocity in gas−liquid systems. The emphasis of this review is to illustrate the present status of the subjects under consideration and to highlight the possible future directions for further understanding of the subject. The bubble formation at a single submerged orifice and on multipoint sieve trays in Newtonian as well as non-Newtonian stagnant and flowing liquids is discussed in detail, which includes its mechanism as well as the effect of several system and operating parameters on the bubble size. The comparison of results has shown that the formulation of Gaddis and Vogelpohl22 is the most suitable for the estimation of bubble size in stagnant liquids. The special cases, such as bubble formation in reduced gravity conditions and weeping and in flowing liquids, are discussed in detail. The section on the rise of a gas bubble in liquid covers the various parameters governing bubble rise and their effect on the rise velocity. A comprehensive comparison of the various formulations is made by validating the predictions with experimental data for Newtonian as well as non-Newtonian liquids, published over last several decades. The results highlight that for the estimation of rise velocity in (i) pure Newtonian liquids, (ii) contaminated Newtonian liquids, and (iii) non-Newtonian liquids, the formulation based on the wave theory by Mendelson,190 Nguyen's formulation,155 and the formulation by Rodrigues,153 (last two, based on the dimensional analysis), respectively are the most suitable. The motion of bubbles in non-Newtonian liquids and the reason behind the discontinuity in the velocity are also discussed in detail. The bubble rise is also analyzed in terms of the drag coefficient for different system parameters and bubble sizes.

Three spiro-OMeTAD derivatives have been synthesized and characterized by (1)H/(13)C NMR spectroscopy and mass spectrometry. The optical and electronic properties of the derivatives were modified by changing the positions of the two methoxy substituents in each of the quadrants, as monitored by UV-vis spectroscopy and cyclic voltammetry measurements. The derivatives were employed as hole-transporting materials (HTMs), and their performances were compared for the fabrication of mesoporous TiO2/CH3NH3PbI3/HTM/Au solar cells. Surprisingly, the cell performance was dependent on the positions of the OMe substituents. The derivative with o-OMe substituents showed highly improved performance by exhibiting a short-circuit current density of 21.2 mA/cm(2), an open-circuit voltage of 1.02 V, and a fill factor of 77.6% under 1 sun illumination (100 mW/cm(2)), which resulted in an overall power conversion efficiency (PCE) of 16.7%, compared to ~15% for conventional p-OMe substituents. The PCE of 16.7% is the highest value reported to date for perovskite-based solar cells with spiro-OMeTAD.

Carbon-based materials are widely employed as metal-free catalysts or supports in catalysis, energy, and ecological applications because of their interesting properties. Generally, their high surface areas, size, shape, porosity, and the possibility of incorporating additional moieties through chemical functional designs are believed to be essential for enriching the catalytic activity of carbon-containing materials. Lately, the new field of single-atom catalysts (SACs) has emerged as the finest alternative for not only homogeneous but also heterogeneous catalysts used in various kinds of catalytic applications. Among a variety of SACs, carbon-based SACs are widely investigated catalysts because of their extraordinary features such as tunable morphologies, ordered porosity, and effortless immobilization through various metals (noble and non-noble), making them highly efficient single-atom catalysts for numerous important catalytic applications. Herein, we intend to report on the progress achieved in researching carbon-based single-atom catalysts, including primarily metals such as Co, Cu, Zn, Pd, Ni, Pt, among others, embedded in carbon matrices and applied to applications in organic catalysis, photocatalysis, and electrocatalysis. It is important to point out that the main focus of this Review is directed to the activity and applications of single-atom catalysts, which are discussed in detail; thus, characterization and rationalization are excluded. Finally, we provide a future perspective on the development and progress made on a carbon-based single metal atom for catalysis.

Layered transition metal dichalcogenides (TMDs) (MoS ₂ , MoSe ₂ , WS ₂ , WSe ₂ , <italic>etc.</italic> ) are a chemically diverse class of compounds having remarkable electrochemical properties.

Bacterial cellulose, an exopolysaccharide produced by some bacteria, has unique structural and mechanical properties and is highly pure as compared to plant cellulose. This article presents a critical review of the available information on the bacterial cellulose with special emphasis on its fermentative production and applications. Information on the biosynthetic pathway of bacterial cellulose, enzymes and precursors involved in bacterial cellulose synthesis has been specified. Characteristics of bacterial cellulose with respect to its structure and physicochemical properties are discussed. Current and potential applications of bacterial cellulose in food, pharmaceutical and other industries are also presented.

The light‐harvesting Sb 2 S 3 surface on mesoporous‐TiO 2 in inorganic–organic heterojunction solar cells is sulfurized with thioacetamide (TA). The photovoltaic performances are compared before and after TA treatment, and the state of the Sb 2 S 3 is investigated by X‐ray diffraction, X‐ray photoelectron spectroscopy, and deep‐level transient spectroscopy (DLTS). Although there are no differences in crystallinity and composition, the TA‐treated solar cells exhibit significantly enhanced performance compared to pristine Sb 2 S 3 ‐sensitized solar cells. From DLTS analysis, the performance enhancement is mainly attributed to the extinction of trap sites, which are present at a density of (2–5) × 10 14 cm −3 in Sb 2 S 3 , by TA treatment. Through such a simple treatment, the cell records an overall power conversion efficiency (PCE) of 7.5% through a metal mask under simulated illumination (AM 1.5G, 100 mW cm –2 ) with a very high open circuit voltage of 711.0 mV. This PCE is, thus far, the highest reported for fully solid‐state chalcogenide‐sensitized solar cells.

Polyurethane is a material that defines the word ‘versatile’. The structure property relationship of di-isocyanates and polyols is such that it provides ample variety and customization to the manufacturer. The properties of the polyurethane can range to extremes from soft touch coatings to rock hard rigid construction material. These mechanical, chemical and biological properties and the ease of tailoring has produced a huge amount of interest in not only the scientific community but also in the concerned industries as well. The enhancement of the material can be done by manipulating the raw materials as well as adding different additives and nanomaterials as well. Proper modifications in the raw material can hence produce a polyurethane virtually suitable for every application. The study here throws light upon the basic chemistry of the building blocks of polyurethane and its recent advancements in applications in fields such as medical science, automobiles, coatings, adhesives, sealants, paints, textile, marine industry, wood composites and apparels.

A set of three N,N-di-p-methoxyphenylamine-substituted pyrene derivatives have successfully been synthesized and characterized by (1)H/(13)C NMR spectroscopy, mass spectrometry, and elemental analysis. The optical and electronic structures of the pyrene derivatives were adjusted by controlling the ratio of N,N-di-p-methoxyphenylamine to pyrene, and investigated by UV/vis spectroscopy and cyclic voltammetry. The pyrene derivatives were employed as hole-transporting materials (HTMs) in fabricating mesoporous TiO2/CH3NH3PbI3/HTMs/Au solar cells. The pyrene-based derivative Py-C exhibited a short-circuit current density of 20.2 mA/cm(2), an open-circuit voltage (Voc) of 0.886 V, and a fill factor of 69.4% under an illumination of 1 sun (100 mW/cm(2)), resulting in an overall power conversion efficiency of 12.4%. The performance is comparable to that of the well-studied spiro-OMeTAD, even though the Voc is slightly lower. Thus, this newly synthesized pyrene derivative holds promise as a HTM for highly efficient perovskite-based solar cells.

Laccases (benzenediol:oxygen oxidoreductase, EC 1.10.3.2) are multi-copper oxidases that are widely distributed among plants, insects, and fungi. They have been described in different genera of ascomycetes, some deuteromycetes, and mainly in basidiomycetes. These enzymes catalyze the one-electron oxidation of a wide variety of organic and inorganic substrates, including mono-, di-, and polyphenols, aminophenols, methoxyphenols, aromatic amines, and ascorbate, with the concomitant four electron reduction of oxygen to water. Laccase is currently the focus of much attention because of its diverse applications, such as delignification of lignocellulosics, crosslinking of polysaccha-rides, bioremediation applications, such as waste detoxification, and textile dye transformation, food technologic uses, personal and medical care applications, and biosensor and analytical applications. This review helps to understand the properties of this important enzyme for efficient utilization for its biotechnological and environmental applications.

Fabricating inorganic-organic hybrid perovskite solar cells (PSCs) on plastic substrates broadens their scope for implementation in real systems by imparting portability, conformability and allowing high-throughput production, which is necessary for lowering costs. Here we report a new route to prepare highly dispersed Zn2SnO4 (ZSO) nanoparticles at low-temperature (<100 °C) for the development of high-performance flexible PSCs. The introduction of the ZSO film significantly improves transmittance of flexible polyethylene naphthalate/indium-doped tin oxide (PEN/ITO)-coated substrate from ∼75 to ∼90% over the entire range of wavelengths. The best performing flexible PSC, based on the ZSO and CH3NH3PbI3 layer, exhibits steady-state power conversion efficiency (PCE) of 14.85% under AM 1.5G 100 mW·cm(-2) illumination. This renders ZSO a promising candidate as electron-conducting electrode for the highly efficient flexible PSC applications.

Abstract Sustainable fiber reinforced polymer (FRP) composites from renewable and biodegradable fibrous materials and polymer matrices are of great interest, as they can potentially reduce environmental impacts. However, the overall properties of such composites are still far from the high‐performance conventional glass or carbon FRP composites. Therefore, a balance between composite performance and biodegradability is required with approaches to what one might call an eco‐friendly composite. This review provides an overview of sustainable FRP composites, their manufacturing techniques, and sustainability in general at materials, manufacturing, and end‐of‐life levels. Sustainable plant‐based natural fibers and polymer matrices are also summarized, followed by an overview of their modification techniques to obtain high‐performance, multifunctional, and sustainable FRP composites. Current state‐of‐the‐art mechanical and functional properties of such composites are then surveyed, and an overview of their potential applications in various industries, including automobile, aerospace, construction, medical, sports, and electronics is provided. Finally, future market trends, current challenges, and the future perspective on sustainable natural FRP composites are discussed.

Beneficial effects are demonstrated by PbI2 incorporated into perovskite materials as a light absorber in solar cells. The PbI2 distributed into the perovskite layers leads to reduced hysteresis and ionic migration, and enables the fabrication of remarkably improved solar cells with a certified power conversion efficiency of 19.75% under air-mass 1.5 global (AM 1.5G) illumination of 100 mW cm−2 intensity. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

The review focuses on recent developments in the synthetic methodologies of COFs and their applications in the field of organocatalysis, electrocatalysis and photocatalysis. Future scope of COFs in the field are also described.

Chemotherapy, a major strategy for cancer treatment, lacks the specificity to localize the cancer therapeutics in the tumor site, thereby affecting normal healthy tissues and advocating toxic adverse effects. Nanotechnological intervention has greatly revolutionized the therapy of cancer by surmounting the current limitations in conventional chemotherapy, which include undesirable biodistribution, cancer cell drug resistance, and severe systemic side effects. Nanoparticles (NPs) achieve preferential accumulation in the tumor site by virtue of their passive and ligand-based targeting mechanisms. Polymer-based nanomedicine, an arena that entails the use of polymeric NPs, polymer micelles, dendrimers, polymersomes, polyplexes, polymer-lipid hybrid systems, and polymer-drug/protein conjugates for improvement in efficacy of cancer therapeutics, has been widely explored. The broad scope for chemically modifying the polymer into desired construct makes it a versatile delivery system. Several polymer-based therapeutic NPs have been approved for clinical use. This review provides an insight into the advances in polymer-based targeted nanocarriers with focus on therapeutic aspects in the field of oncology.

A variety of mixed metal oxides (MMOs), containing alkali, alkaline, rare earth and noble metals, and their applications are presented. In this mini review, we summarize versatile applications of mixed metal oxides in organic synthesis. A variety of reactions such as reduction, oxidation, multicomponent, Mannich, alkylation, condensation, deprotection, cycloaddition, hydroxylation, dehydration, dehydrogenation, transesterification, reactions involving biomimetic oxygen-evolving catalysts and other important C–C bond forming reactions are well presented on the surface of mixed metal oxides under a variety of reaction conditions. The scope of MMOs in important organic reactions, industrial applications, and green chemistry and recent applications of MMOs are well presented in this review.

The photocatalyst-enzyme coupled system for artificial photosynthesis process is one of the most promising methods of solar energy conversion for the synthesis of organic chemicals or fuel. Here we report the synthesis of a novel graphene-based visible light active photocatalyst which covalently bonded the chromophore, such as multianthraquinone substituted porphyrin with the chemically converted graphene as a photocatalyst of the artificial photosynthesis system for an efficient photosynthetic production of formic acid from CO(2). The results not only show a benchmark example of the graphene-based material used as a photocatalyst in general artificial photosynthesis but also the benchmark example of the selective production system of solar chemicals/solar fuel directly from CO(2).