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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/41192">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41192</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/41206" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/41205" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/41204" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/41203" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-09T23:00:43Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/41206">
    <title>Graphene oxide-supported gold nanocomposites for highly sensitive sandwich immunosensor for α-fetoprotein detection</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41206</link>
    <description>Title: Graphene oxide-supported gold nanocomposites for highly sensitive sandwich immunosensor for α-fetoprotein detection
Authors: Li, Pengjun; Lai, Juanhua; Qiu, Ping
Abstract: A graphene oxide-Au NPs sensor platform combined with a multiple-enzyme labeled detection antibody-carbon sphere bioconjugate has been used as the basis for an ultrasensitive electrochemical immunosensor to detect the cancer biomarker, α-fetoprotein (AFP). Greatly enhanced sensitivity has been achieved by using the bioconjugates featuring horseradish peroxidase (HRP) and Ab2 linked to carbon nanospheres (Ab2-HRP-Au-PDA-carbon sphere) at a high ratio of HRP/Ab2. After a sandwich immunoreaction, the Ab2-HRP-Au-PDA-carbon sphere captured onto the electrode surface produces an amplified electrocatalytic response due to the reduction of enzymatically oxidized thionine in the presence of hydrogen peroxide. The increase of response current is proportional to the AFP concentration in the range of 0.01-20 ng/mL, with &#xD;
the detection limit of 3 pg/mL. This amplification strategy is a promising platform for detection of other proteins and &#xD;
clinical applications.
Page(s): 365-372</description>
    <dc:date>2017-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/41205">
    <title>Microwave assisted transesterification of waste cooking oil over modified forms of zirconia coated on honeycomb monolith</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41205</link>
    <description>Title: Microwave assisted transesterification of waste cooking oil over modified forms of zirconia coated on honeycomb monolith
Authors: Vasantha, V T; Shamshuddin, S Z Mohamed; Serrao, Reena Saritha; D’Souza, Joyce Queeny
Abstract: Microwave assisted transesterification of waste cooking oil over honeycomb monoliths coated with zirconia based catalysts such as MgO/ZrO&lt;sub&gt;2&lt;/sub&gt; and CaO/ZrO&lt;sub&gt;2&lt;/sub&gt; to synthesize biodiesel is reported. For comparison, biodiesel synthesis via transesterification using conventional heating method has also been carried out. The solid acid Al&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;/ZrO&lt;sub&gt;2&lt;/sub&gt; coated on a honeycomb has also been used as a catalyst to reduce the percentage of free fatty acid in waste cooking oil via esterification using conventional heating. The honeycomb monoliths have been coated with solid bases and characterized for their physico-chemical properties such as surface acidity, surface basicity, crystalinity and morphology using suitable techniques. The honeycomb monoliths coated with solid catalysts are found to be highly efficient and reusable in the process of synthesizing biodiesel from waste cooking oil. A maximum yield of biodiesel (98%) is obtained at 60 &amp;deg;C in 10 min by keeping the molar ratio of oil:methanol ratio at 1:6 under microwave irradiation.
Page(s): 373-378</description>
    <dc:date>2017-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/41204">
    <title>Catalytic activity of niobia supported graphene oxide for  esterification of oleic acid</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41204</link>
    <description>Title: Catalytic activity of niobia supported graphene oxide for  esterification of oleic acid
Authors: Kanimozhi, S; Pandurangan, A; Hemalatha, P
Abstract: Biodiesel has been obtained from esterification of oleic acid with methanol using niobia loaded graphene oxide (GO). Different weight percentages of niobia (1, 3, 5 and 7 wt.%) have been loaded on GO by the wet impregnation method. The synthesized materials have been characterized by XRD, FT-IR, Raman spectroscopy, TGA, BET surface area, NH&lt;sub&gt;3&lt;/sub&gt;-TPD,  ICP-OES, SEM and HR-TEM studies. The catalytic activity of niobia supported on GO has been tested for esterification of oleic acid with methanol for biodiesel production. The maximum yield of methyl oleate (96.4%) is obtained at the reaction conditions of 150 &amp;deg;C, 0.5 g of 5 wt% of niobia on GO catalyst, 1:9 molar ratio of oleic acid:methanol and time 4 h. Influence of solvents (ethanol, propanol, butanol) has been tested for comparative study with same reaction conditions. Based on the catalytic studies, niobia supported GO has good catalytic activity for esterification of oleic acid reaction with good reusability.
Page(s): 379-386</description>
    <dc:date>2017-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/41203">
    <title>On the syntheses and structures of two calcium coordination polymers containing terminal amide ligands</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/41203</link>
    <description>Title: On the syntheses and structures of two calcium coordination polymers containing terminal amide ligands
Authors: Srinivasan, Bikshandarkoil R; Dhavskar, Kiran T
Abstract: The syntheses and crystal structure of the calcium coordination polymers [Ca(NMF)&lt;sub&gt;2&lt;/sub&gt;(4-nba)&lt;sub&gt;2&lt;/sub&gt;] &lt;strong&gt;1&lt;/strong&gt; (4-nba = 4-nitrobenzoate; NMF=N-methylformamide) and [Ca(BA)&lt;sub&gt;2&lt;/sub&gt;(4-nba)&lt;sub&gt;2&lt;/sub&gt;] &lt;strong&gt;2&lt;/strong&gt; (BA= benzamide) is reported. A unique &amp;mu;&lt;sub&gt;2&lt;/sub&gt;-&amp;eta;&lt;sup&gt;1&lt;/sup&gt;: &amp;eta;&lt;sup&gt;1 &lt;/sup&gt;bridging bidentate 4-nba ligand links the hexacoordinated Ca(II) ions situated on a special position in both compounds into a one-dimensional (1-D) chain with Ca&amp;middot;&amp;middot;&amp;middot;Ca separations of 5.561 and 5.482 respectively. Each Ca(II) in the chain is bonded to a pair of symmetry related terminal amide ligands (NMF in &lt;strong&gt;1&lt;/strong&gt;; BA in &lt;strong&gt;2&lt;/strong&gt;) which are disposed &lt;em&gt;trans&lt;/em&gt; to each other. A comparative study of several 4-nitrobenzoates of calcium is described.
Page(s): 387-393</description>
    <dc:date>2017-04-01T00:00:00Z</dc:date>
  </item>
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