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      Novel green synthesis of S-doped TiO2 nanoparticles using Malva parviflora plant extract and their photocatalytic, antimicrobial and antioxidant activities under sunlight illumination

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      Chemosphere
      Elsevier BV

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          Principles and mechanisms of photocatalytic dye degradation on TiO2 based photocatalysts: a comparative overview

          Pictorial representation of all possible dye degradation reaction in UV light initiated indirect dye degradation mechanism. This mechanism is practically more important over visible light initiated direct mechanism. The total annual production of synthetic dye is more than 7 × 10 5 tons. Annually, through only textile waste effluents, around one thousand tons of non-biodegradable textile dyes are discharged into natural streams and water bodies. Therefore, with growing environmental concerns and environmental awareness there is a need for the removal of dyes from local and industrial water effluents with a cost effective technology. In general, these dyes have been found to be resistant to biological as well as physical treatment technologies. In this regard, heterogeneous advanced oxidation processes (AOPs), involving photo-catalyzed degradation of dyes using semiconductor nanoparticles is considered as an efficient cure for dye pollution. In the last two decades TiO 2 has received considerable interest because of its high potential as a photocatalyst to degrade a wide range of organic material including dyes. This review starts with (i) a brief overview on dye pollution, dye classification and dye decolourization/degradation strategies; (ii) focuses on the mechanisms involved in comparatively well understood TiO 2 photocatalysts and (iii) discusses recent advancements to enhance TiO 2 photocatalytic efficiency by (a) doping with metals, non-metals, transition metals, noble metals and lanthanide ions, (b) structural modifications of TiO 2 and (c) immobilization of TiO 2 by using various supports to make it a flexible and cost-effective commercial dye treatment technology.
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            Green chemistry for nanoparticle synthesis.

            The application of the twelve principles of green chemistry in nanoparticle synthesis is a relatively new emerging issue concerning the sustainability. This field has received great attention in recent years due to its capability to design alternative, safer, energy efficient, and less toxic routes towards synthesis. These routes have been associated with the rational utilization of various substances in the nanoparticle preparations and synthetic methods, which have been broadly discussed in this tutorial review. This article is not meant to provide an exhaustive overview of green synthesis of nanoparticles, but to present several pivotal aspects of synthesis with environmental concerns, involving the selection and evaluation of nontoxic capping and reducing agents, the choice of innocuous solvents and the development of energy-efficient synthetic methods.
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              Green Synthesis of Bifunctional Fluorescent Carbon Dots from Garlic for Cellular Imaging and Free Radical Scavenging.

              Nitrogen and sulfur codoped carbon dots (CDs) were prepared from garlic by a hydrothermal method. The as-prepared CDs possess good water dispersibility, strong blue fluorescence emission with a fluorescent quantum yield of 17.5%, and excellent photo and pH stabilities. It is also demonstrated that the fluorescence of CDs are resistant to the interference of metal ions, biomolecules, and high ionic strength environments. Combining with low cytotoxicity properties, CDs could be used as an excellent fluorescent probe for cellular multicolor imaging. Moreover, the CDs were also demonstrated to exhibit favorable radical scavenging activity.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Chemosphere
                Chemosphere
                Elsevier BV
                00456535
                May 2021
                May 2021
                : 271
                : 129524
                Article
                10.1016/j.chemosphere.2020.129524
                f8fe219b-9d84-4b01-a098-2a6361801e00
                © 2021

                https://www.elsevier.com/tdm/userlicense/1.0/

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