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    <title>DSpace Collection:</title>
    <link>http://10.9.150.37:8080/dspace//handle/atmiyauni/505</link>
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    <pubDate>Mon, 27 Apr 2026 18:57:29 GMT</pubDate>
    <dc:date>2026-04-27T18:57:29Z</dc:date>
    <item>
      <title>Eco-friendly process for preparation of biodiesel from WFO over MTSA-Si catalyst: An innovative approach for the utilization of side product</title>
      <link>http://10.9.150.37:8080/dspace//handle/atmiyauni/980</link>
      <description>Title: Eco-friendly process for preparation of biodiesel from WFO over MTSA-Si catalyst: An innovative approach for the utilization of side product
Authors: Savaliya, Mehulkumar L.; Dholakiya, Bharatkumar Z.
Abstract: Present work aimed for the synthesis of a promising MTSA-Si catalyst and its application for biodiesel preparation using WFO. It has been illustrated from the experimental results, the most favorable reaction conditions&#xD;
for the biodiesel preparation using WFO are (i) 1:10 oil to methanol molar ratio, (ii) 5% MTSA-Si catalyst&#xD;
(w/w), (iii) 130 °C reaction temperature and (iv) 10 h reaction time, for the 98.22% yield of biodiesel. The&#xD;
side product raw glycerin was further transformed into the triglycerides over MTSA-Si catalyzed lauric acid&#xD;
esterification. The fuel properties of biodiesel were estimated and correlated fuel standards.
Description: Authors are gratefully acknowledging the financial assistance from&#xD;
SVNIT, Surat and CSIR, New Delhi, India (Sanction Order Letter No.&#xD;
02(0170)/13/EMR-II). For analytical services, we wish to thank, Applied Chemistry Department, SVNIT Surat, Mr. Sagar, MED, SVNIT,&#xD;
Surat, A. Narayanan, Indian Institute of Technology, Madras, and&#xD;
Prof. Anamik Shah, Center of Excellence in Drug Discovery, Saurashtra University, Rajkot, Gujarat, India.</description>
      <pubDate>Mon, 01 Jan 2018 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://10.9.150.37:8080/dspace//handle/atmiyauni/980</guid>
      <dc:date>2018-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Energy from industrial waste as a substitute for fuel &amp; utilization of pollutant co2 produced for algae formation</title>
      <link>http://10.9.150.37:8080/dspace//handle/atmiyauni/978</link>
      <description>Title: Energy from industrial waste as a substitute for fuel &amp; utilization of pollutant co2 produced for algae formation
Authors: Tank, Ravi S.; Puranik, S.A.
Abstract: Industrial  based  research  project  using  different types of  solid/liquid waste  for energy  generation and  replacing conventional  fuel-coal  partially  by  solid/liquid  waste  has  been investigated.  Pollutant  produced  CO2  during  combustion  of solid/liquid  waste  can  be  utilized  conveniently  for  algae cultivation.  Further  algae  so  cultivated  can  be  converted  into energy either in the form of carbohydrates or lipids. This can be further converted into  bio-fuels  like bio-ethanol  and bio-diesel. All these aspects  have been  analyzed critically in  this paper  for typical  Cement  Manufacturing  Unit  wherein  fuel  utilized-coal has been partially substituted by solid/liquid waste.  Further,  use of  hydrogen as  a  fuel-an alternative  clean fuel  of tomorrow has also been highlighted in this research project.</description>
      <pubDate>Fri, 01 Mar 2013 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://10.9.150.37:8080/dspace//handle/atmiyauni/978</guid>
      <dc:date>2013-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Water mediated synthesis of highly functionalized pyrazolone derivatives using tetraethylammoniumbromide</title>
      <link>http://10.9.150.37:8080/dspace//handle/atmiyauni/974</link>
      <description>Title: Water mediated synthesis of highly functionalized pyrazolone derivatives using tetraethylammoniumbromide
Authors: Savant, Mahesh M.; Pansuriya, Akshay M.; Naliapara, Yogesh T.
Abstract: An efficient, cleaner and environment benign Knoevenagel condensation of aromatic aldehydes with 3-methyl-5-pyrazolone using TEAB in water media is described. The reaction is highly chemoselective with no side reactions. The &#xD;
procedure does not involve the use of any additional reagent/catalyst, produces no waste, and represents a green &#xD;
synthetic protocol.
Description: Authors are thankful for facilities &amp; grants given &#xD;
under UGC-SAP for Department Research Support &#xD;
(DRS) and Department of Science &amp; Technology (DST) &#xD;
New Delhi for Fund for Improvement of Science &amp; &#xD;
Technology (FIST) and Department of Chemistry for &#xD;
providing laboratory facilities.</description>
      <pubDate>Wed, 01 Oct 2014 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://10.9.150.37:8080/dspace//handle/atmiyauni/974</guid>
      <dc:date>2014-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis, characterization, crystal, and molecular structure analysis of 3,4- dihydro-6-(2-hydroxyphenyl)-5-nitro-4- phenylpyrimidin-2(1H)-one</title>
      <link>http://10.9.150.37:8080/dspace//handle/atmiyauni/972</link>
      <description>Title: Synthesis, characterization, crystal, and molecular structure analysis of 3,4- dihydro-6-(2-hydroxyphenyl)-5-nitro-4- phenylpyrimidin-2(1H)-one
Authors: Savant, M.M.; Gowda, L.B.; Anandalwar, S.M.; Prasad, J.S.; Shah, A.; Naliapara, Y.T.
Abstract: A novel nitro and 2-hydroxyphenyl functionalized pyrimidinone at C5 and C6, respectively, has been synthesized using 1-(2-hydroxyphenyl)-2-nitroethanone, benzaldehyde,&#xD;
urea, and etidronic acid as a catalyst is described. The synthesized compound characterized by spectroscopic techniques and finally confirmed by X-ray diffraction studies. The&#xD;
molecule crystallizes in the monoclinic crystal class in the space group P21/c with cell&#xD;
parameters a = 11.1070(10)Å, b = 8.8210(4)Å, c = 15.1110(13)Å, β = 106.193(2)◦,&#xD;
and Z = 4. The pyrimidine ring adopts flattened boat conformation.
Description: The authors are thankful to FIST-DST, SAP-UGC for their generous financial and instrumentation support. Special thanks are due to “National Facility for Drug Discovery through&#xD;
New Chemical Entities Development &amp; Instrumentation Support to Small Manufacturing&#xD;
Pharma Enterprises” Programme under Drug &amp; Pharma Research Support jointly funded by&#xD;
DST &amp; Government of Gujarat Industries Commissionerate. Government of India project&#xD;
SP/I2/FOO/93 and University of Mysore, Mysore for financial assistance.</description>
      <pubDate>Sat, 11 Apr 2015 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://10.9.150.37:8080/dspace//handle/atmiyauni/972</guid>
      <dc:date>2015-04-11T00:00:00Z</dc:date>
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