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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/40900</link>
    <description />
    <pubDate>Fri, 09 Oct 2026 16:29:34 GMT</pubDate>
    <dc:date>2026-10-09T16:29:34Z</dc:date>
    <item>
      <title>On the current status of the mechanistic aspects of photocatalytic  reduction of carbon dioxide</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40911</link>
      <description>Title: On the current status of the mechanistic aspects of photocatalytic  reduction of carbon dioxide
Authors: Narayanan, Hariprasad; Nair, M V Harindranathan; Viswanathan, Balasubramanian
Abstract: Photocatalytic reduction of carbon dioxide, one of the pathways involved in the carbon dioxide conversion process,  has been receiving significant attention from the scientific community in the last four decades. Nevertheless, the mechanism of carbon dioxide reduction is still unclear and the information available is not sufficient for developing it into large scale applications, possibly because of the invariable hurdles associated with the reduction process. The reductive photocatalytic conversion of CO&lt;sub&gt;2&lt;/sub&gt; involves all the redox reactions occurring at the interface of the semiconductor such as water splitting, hydrogen evolution, oxygen evolution, photo-oxidation reactions and reactions of radical intermediates. The overall product yield is highly dependent on the extent of these competing reactions. Herein, we discuss our perceptions and current status of the interface reactions and their involvement in the fundamental mechanistic aspects of the photocatalytic conversion of CO&lt;sub&gt;2&lt;/sub&gt;.
Page(s): 251-269</description>
      <pubDate>Wed, 01 Mar 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40911</guid>
      <dc:date>2017-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Photocatalytic and DC conductivity studies of proton exchanged KAl&lt;sub&gt;0.33&lt;/sub&gt;W&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; and its application in Pb&lt;sup&gt;2+&lt;/sup&gt; removal</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40910</link>
      <description>Title: Photocatalytic and DC conductivity studies of proton exchanged KAl&lt;sub&gt;0.33&lt;/sub&gt;W&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; and its application in Pb&lt;sup&gt;2+&lt;/sup&gt; removal
Authors: Srinivas, M; Ravi, G; Kumar, P Vijaya; Reddy, CH Sudhakar; Sreenu, K; Guje, Ravinder; Vithal, M
Abstract: The proton exchanged metal oxide of composition HAl&lt;sub&gt;0.33&lt;/sub&gt;Te&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; (HAW) is synthesized by ion exchange method at room temperature and characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy and UV-vis diffuse reflectance spectroscopy. Presence of water content in the HAW has been examined by thermogravimetric analysis. Conductivity and photocatalytic properties of HAW are compared with those of its parent KAl&lt;sub&gt;0.33&lt;/sub&gt;W&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; (KAW). HAl&lt;sub&gt;0.33&lt;/sub&gt;W&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; shows higher conductivity and photocatalytic activity for the degradation of methyl blue and Rhodamine B under visible light irradiation. Participation of hydroxyl radicals in the photocatalytic dye degradation has been investigated by photoluminescence studies using terephthalic acid as probe. The removal of Pb&lt;sup&gt;2+&lt;/sup&gt; from an aqueous solution of Pb(NO&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt; using pristine KAl&lt;sub&gt;0.33&lt;/sub&gt;W&lt;sub&gt;1.67&lt;/sub&gt;O&lt;sub&gt;6&lt;/sub&gt; is also reported.
Page(s): 270-277</description>
      <pubDate>Wed, 01 Mar 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40910</guid>
      <dc:date>2017-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Surfactant assisted synthesis of cobalt doped titania nanomaterial: Characterization and its applications in photocatalysis and anti-bacterial activity</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40909</link>
      <description>Title: Surfactant assisted synthesis of cobalt doped titania nanomaterial: Characterization and its applications in photocatalysis and anti-bacterial activity
Authors: Chekuri, Radha Devi; Tirukkovalluri, Siva Rao
Abstract: The synthesis of 0.5 wt. % cobalt doped titania nanomaterial (Co&lt;sup&gt;2+&lt;/sup&gt;-TiO&lt;sub&gt;2&lt;/sub&gt;) assisted by sodium dodecyl sulfate anionic surfactant by sol-gel method is reported. The synthesized catalysts are characterized by XRD, UV-vis DRS, FT-IR, BET, TEM, SEM and XPS analysis. XRD results show that all the catalysts are in anatase phase. UV-vis DRS studies indicate that decrease in band gap of TiO&lt;sub&gt;2&lt;/sub&gt; is due to doping of Co&lt;sup&gt;2+&lt;/sup&gt;. FT-IR studies indicate the insertion of Co&lt;sup&gt;2+&lt;/sup&gt; into TiO&lt;sub&gt;2 &lt;/sub&gt;lattice as a substitutional dopant. BET analysis shows an increase in surface area of the catalyst. From SEM and TEM analysis, change in the morphology of the particles with reduced particle size is observed. XPS studies confirm the presence of Co&lt;sup&gt;2+ &lt;/sup&gt;along with Ti and O. The photocatalytic efficiency of the catalyst has been evaluated by degradation of methyl red under visible light irradiation at various reaction parameters. The antibacterial activity of the catalyst against &lt;em&gt;Escherichia&lt;/em&gt; &lt;em&gt;coli&lt;/em&gt; has also been investigated.
Page(s): 278-286</description>
      <pubDate>Wed, 01 Mar 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40909</guid>
      <dc:date>2017-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Combined effect of adsorbent chitosan and photosensitizer polypyrrole in ternary chitosan-polypyrrole-TiO&lt;sub&gt;2&lt;/sub&gt; photocatalyst leading to visible light activity and superior functionality</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/40908</link>
      <description>Title: Combined effect of adsorbent chitosan and photosensitizer polypyrrole in ternary chitosan-polypyrrole-TiO&lt;sub&gt;2&lt;/sub&gt; photocatalyst leading to visible light activity and superior functionality
Authors: Murugan, C; Subramanian, E
Abstract: The combined effect of the components in the ternary chitosan-polypyrrole-TiO&lt;sub&gt;2&lt;/sub&gt; (Chit-Ppy-TiO&lt;sub&gt;2&lt;/sub&gt;) photocatalytic system has been investigated. The role of each component in this catalyst is validated by the visible light degradation of the model dye methylene blue. The reaction parameters, viz., amount of catalyst, dye concentration, oxidant concentration and temperature are studied in detail. The ternary system exhibits greater activity when compared to both the single and binary component catalysts (chitosan-TiO&lt;sub&gt;2&lt;/sub&gt; and polypyrrole-TiO&lt;sub&gt;2&lt;/sub&gt;). The superior functionality of Chit-Ppy-TiO&lt;sub&gt;2&lt;/sub&gt; (1:1:100 wt ratio) originates from the combined effect of greater dye adsorption of chitosan, visible light sensitization of polypyrrole and the catalytic functionality of TiO&lt;sub&gt;2&lt;/sub&gt;. The ternary photocatalyst is recyclable even after fourth  run without appreciable loss in its activity.
Page(s): 287-296</description>
      <pubDate>Wed, 01 Mar 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/40908</guid>
      <dc:date>2017-03-01T00:00:00Z</dc:date>
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