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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Manganese Oxide Doped Noble Metals Supported Catalyst for Carbon Dioxide Methanation Reaction</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3372</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>R.</FirstName>
					<LastName>Ali</LastName>
<Affiliation>Department of Chemistry,Kuwait University</Affiliation>

</Author>
<Author>
					<FirstName>W. A. W.</FirstName>
					<LastName>Abu Bakar</LastName>
<Affiliation>Department of Chemistry,University of Mashad</Affiliation>

</Author>
<Author>
					<FirstName>Najwa</FirstName>
					<LastName>Sulaiman</LastName>
<Affiliation>Department of Chemistry,University of Kansas</Affiliation>

</Author>
<Author>
					<FirstName>Hazwan Faiz</FirstName>
					<LastName>Abd Rahim</LastName>
<Affiliation>Department of Chemistry,University of Kansas</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>Manganese oxide supported on alumina was prepared for methanation reaction by doping
the manganese oxide based catalyst with noble metals, namely ruthenium, Ru and palladium, and Pd,
via an impregnation method. The potential catalyst was calcined at 400C, 700C and 1000C for 5
hours separately. An in-house-built micro reactor with an FTIR detector and GC was used to study the
percentage of CO2 conversion and also the percentage of CH4 formation. Ru/Mn (30:70)-Al2O3 calcined
at 1000C was the potential catalyst, which gave 86.82% CO2 conversion and 61.94% CH4 yield at a
reaction temperature of 200C. XRD analysis showed that the catalyst is of a crystalline phase, while
FESEM illustrated the catalyst surface was covered with small and dispersed particles with an undened
shape. EDX analysis revealed that there was 21.15% reduction of Ru in the spent catalyst compared to the
fresh catalyst due to the migration of Ru particles into the porous support during the reaction. There was
5.39% reduction of surface area over the spent Ru/Mn (30:70)-Al2O3 catalyst, characterized by Nitrogen
Adsorption analysis. FTIR analysis revealed that the catalyst surface is hydrated.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Manganese oxide</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Methanation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Ruthenium</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Palladium</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Catalyst</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3372_91b0f2e16c679a2fc12d115c2f3b4b6c.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Epoxidation of Olefins Catalyzed by Some cis-Dioxomolybdenum(VI)-Tridentate Schi Base Complexes with tert-Butyl Hydroperoxide</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3373</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>M.</FirstName>
					<LastName>Bagherzadeh</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>S.</FirstName>
					<LastName>Ghazali Esfahani</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>Some cis-dioxomolybdenum (VI) complexes with tridentate Schi base ligands derived from
salicylaldehyde and aminophenols, aminoalcohol or o-aminobenzenethiol were examined as catalysts for
epoxidation of dierent aliphatic and aromatic olens, with tert-butyl hydroperoxide as oxidant. All
complexes exhibited high activity and selectivity for epoxidation of aliphatic substrates during a short time
period (95% conversion of cyclooctene after 30 min). The epoxide yield increased with the nucleophilic
character of olen. The catalysts activation strongly depends on the reaction temperature and nature of
the solvent. Epoxidation of olens by these catalysts is inhibited by ligands or coordinating solvents such
as alcohols.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Epoxidation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Olen</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cis-dioxomolybdenum complexes</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Tridentate Schi base ligands</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">tertbutyl hydroperoxide</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3373_0c9e72c2a808ff87458a4f83d19829a5.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Photodegradation of N-Methyldiethanolamine over ZnO/SnO2 Coupled Photocatalysts</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3374</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>R.</FirstName>
					<LastName>Ali</LastName>
<Affiliation>Department of Chemistry,Kuwait University</Affiliation>

</Author>
<Author>
					<FirstName>W. A. W.</FirstName>
					<LastName>Abu Bakar</LastName>
<Affiliation>Department of Chemistry,University of Mashad</Affiliation>

</Author>
<Author>
					<FirstName>S.S.</FirstName>
					<LastName>Mislan</LastName>
<Affiliation>Department of Chemical Processes Developmant and Engineering,British Nuclear Fuels Ltd</Affiliation>

</Author>
<Author>
					<FirstName>M.A.</FirstName>
					<LastName>Sharifuddin</LastName>
<Affiliation>Department of Chemistry,British Nuclear Fuels Ltd</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>A photocatalyst semiconductor can be used to remove organic pollutants from wastewater
in the presence of UV light. In this research, coupled ZnO/SnO2 semiconductors with 1:1 and 2:1 ratios
were prepared using the co-precipitation method. The prepared coupled ZnO/SnO2 photocatalyst was
tested towards the photodegradation of simulated N-Methyldiethanolamine (MDEA) under UV-irradiation
( = 365 nm, 100 V, 6 W). The ZnO/SnO2 was characterized using UV diused re
ectance spectroscopy
and X-ray diraction. The band gap energy for ZnO/SnO2 (ZS) catalyst calcined at 200C, 400C,
600C and 900C were 3.22, 3.13, 3.12 and 3.07 eV, respectively, while for Z2S were 3.71, 3.28, 3.16,
and 3.14 eV, respectively. XRD results indicated that ZS and Z2S catalysts possessed mixed phases of ZnO,
SnO2 and Zn2SnO4 at a calcinations temperature above 600C. The ZnO/SnO2 (2:1) catalyst, which was
calcined at 600C for 9 hours, gave the optimum percentage photodegradation of MDEA with 39.18%.
The percentage degradation of MDEA was measured using ion chromatography with retention time at the
measured peak of 4-5 minutes. The optimum system was applied on the photodegradation of MDEA in
petroleum wastewater. The percentage degradation of MDEA in petroleum wastewater was 23.38 %.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">ZnO</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">SnO2</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">MDEA</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Photocatalyst</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Photodegradation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Band gap energy</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3374_0342b1a63474c1ba6b00d85db4a7cf71.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>XRD, AFM and UV-Vis Optical Studies of PbSe Thin Films Produced by Chemical Bath Deposition Method</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3375</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Soon Min</FirstName>
					<LastName>Ho</LastName>
<Affiliation>Department of Chemistry,University of Maryland</Affiliation>

</Author>
<Author>
					<FirstName>Anuar</FirstName>
					<LastName>Kassim</LastName>
<Affiliation>Department of Chemistry,Macquarie University</Affiliation>

</Author>
<Author>
					<FirstName>Abdul Halim</FirstName>
					<LastName>Abdullah</LastName>
<Affiliation>Department of Chemistry,Macquarie University</Affiliation>

</Author>
<Author>
					<FirstName>Saravanan</FirstName>
					<LastName>Nagalingam</LastName>
<Affiliation>Department of Chemistry,Macquarie University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>PbSe thin films have been deposited on microscope glass substrates by chemical bath
deposition technique. The chemical bath consisted of lead nitrate, sodium selenate and triethanolamine
solutions. The in
uence of bath temperature on the properties of PbSe lms was investigated. The X-ray
diffraction, atomic force microscope and UV/Vis Spectrophotometer were used to obtain the structural
characterization, surface morphological and absorbance data, respectively. Based on the X-ray diraction
results, the thin lms obtained were found to be polycrystalline in nature with cubic structure. The
intensity of the (111) peak showed a signicant increased as the bath temperature was increased from 40
to 80C. The lms deposited at 80C indicated that the crystallinity was improved and more PbSe peaks
were observed. On the other hand, the grain size, lm thickness and surface roughness were increased
while band gap energy decreased as could be observed in atomic force microscope and UV-Vis optical
studies, respectively.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Lead selenide</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">X-ray diraction</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Optical properties</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Chemical bath deposition</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Thin lms</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3375_d85cbf0c28886e03afc40d7d3c334067.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Separation and Preconcentration of Ultra Traces of Some Heavy Metals in Environmental Samples by Electrodeposition Technique Prior to Flame Atomic Absorption Spectroscopy Determination (ED-FAAS)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3376</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>N.</FirstName>
					<LastName>Mashkouri Najafi</LastName>
<Affiliation>Department of Chemistry,Shahid Beheshti University</Affiliation>

</Author>
<Author>
					<FirstName>Parmis</FirstName>
					<LastName>Shakeri</LastName>
<Affiliation>Department of Chemistry,Shahid Beheshti University</Affiliation>

</Author>
<Author>
					<FirstName>Ensieh</FirstName>
					<LastName>Ghasemi</LastName>
<Affiliation>Department of Chemistry,Shahid Beheshti University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>In this approach, electrodeposition was developed for separation of ultra traces of some
heavy metals from the complex matrices prior to determination by 
ame atomic absorption spectroscopy.
The electrodeposition is carried out at optimized parameters of pH and temperature of electrolyte, voltage
and duration time of deposition. The calculated LOD for ED-FAAS for the interested elements was found
as follows: 1.27 ng mL????1 for Co, 0.14 g mL????1 for Re, 1.56 ng mL????1 for Ni, 1.84 ng mL????1 for Au,
0.02 g mL????1 for Pt and 6.67 ng mL????1 for In. Characteristic concentration for Co, Re, Ni, Au, Pt and
In in ED-FAAS technique are 1.72, 660, 2.67, 2.99, 30 and 9.60 ng mL????1 with %RSD as 1.54, 2.69,
2.45, 2.77, 2.38 and 2.55, respectively. These elements were measured in some environmental samples.
Concentration of Co and Ni in a mineral water are 12.46 and 21.43 ng mL????1, respectively, concentration
of Re in a molybdenum mineral concentrate is 4.65 g mL????1, concentration of Au in a geological samples
is 6.00 ng mL????1. It was also found that the recovery test for spiked Pt and In to a waste water samples
is promising using the proposed technique.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Heavy metal</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Environmental sample</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Electrodeposition</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Preconcentration</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Flame atomic absorption spectroscopy</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3376_5a12a5045f9786e909afe7ea60ec28f1.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparison of Solid Substrate and Submerged Fermentation for Chitosan Production by Aspergillus niger</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3377</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>S.</FirstName>
					<LastName>Yaghmaei</LastName>
<Affiliation>Department of Chemical and Petrochemical Engineering,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>V.</FirstName>
					<LastName>Maghsoodi</LastName>
<Affiliation>Biochemical and Bioenvironmental Research Center,Sharif University of Technology</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>Production yield of solid-state (SSF) and submerged fermentation (SMF) on chitosan from
Aspergillus niger was investigated. A. niger BBRC 20004 was grown on soybean residue and Sabouraud
Dextrose Broth medium (2% glucose). Chitosan was extracted from the fungal mycelia using hot alkaline
and acid treatment. Soybean residue at a moisture content of 37%, and 8.4  0.26% of nitrogen content
produced the highest amount of chitosan, 17.053  0.95 g/kg dry substrate after 12 days. Also, chitosan
was extracted from A. niger on Sabouraud Dextrose Broth medium in submerged fermentation (0.8455 g/l
after 12 days of cultivation). The yield of chitosan isolated in SSF was about 15-20 times more than in
SMF (Submerged Fermentation).
Keyword: Chitosan; Soybean residue; Solid-State Fermentation (SSF); Submerged Fermentation (SMF);
Sabouraud Dextrose Broth (SDB); Glucose; Aspergillus niger.</Abstract>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3377_10f1bad7bc76d0a82c1cabf904c2aed3.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Modeling of Methane and Propane Hydrate Formation Kinetics Based on Chemical Afinity</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3378</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>A. A.</FirstName>
					<LastName>Izadpanah</LastName>
<Affiliation>Department of Chemical Engineering,Guilan University</Affiliation>

</Author>
<Author>
					<FirstName>F.</FirstName>
					<LastName>Varaminian</LastName>
<Affiliation>Department of Chemical Engineering,Semnan University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>In this study, experimental data on the kinetics of methane and propane hydrate formation
at constant volume were collected. The experiments were carried out in a batch reactor under different
temperatures and pressures. The chemical anity was used for modeling of the hydrate formation rate
in a constant volume process. In this method, the system was considered as a classical thermodynamic or
macroscopic view. The results show that this method can predict constant volume experimental data well
for both crystals I and II hydrate former.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Chemical anity</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Methane</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Propane</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Formation kinetics</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Gas hydrates</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3378_922e9a5c94f7e20dcc67888ef11be762.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of Operation Conditions on the Catalytic Performance of the Co/Mn/TiO2 Catalyst for Conversion of Synthesis Gas to Light Olens</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3379</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>D.</FirstName>
					<LastName>Rashtchian</LastName>
<Affiliation>Department of Chemical Engineering,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>R.</FirstName>
					<LastName>Bozorgmehry Boozarjomehry</LastName>
<Affiliation>Department of Chemical Engineering,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>C.</FirstName>
					<LastName>Ghotbi</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>F.</FirstName>
					<LastName>Shayegh</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>The eect of operation variables, such as the H2/CO molar feed ratio, gas hourly space
velocity (GHSV), temperature, and pressure, on the catalytic performance of the Co/Mn/TiO2 catalyst
prepared at the Research Institute of the Petroleum Industry (RIPI) was investigated, and optimum reactor
conditions were obtained to produce the maximum amount of light olens. The catalyst was prepared by
co-precipitation of Co and Mn phases in the presence of commercial TiO2 with maximum selectivity
for ethylene and propylene production. It was found that the [H2]/[CO]=2/1, space velocity (GHSV)
of 1800 h????1, 280C temperature and 4 bar pressure were optimum operating conditions for the modied
catalyst for the conversion of Synthesis Gas(SG) to light olens. The results were interpreted in terms of
the structure of the catalyst. Characterizations of catalysts were carried out using XRD, SEM and BET
specic surface area.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Operation condition</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Co-precipitation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cobalt manganese oxide catalyst</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fischer-Tropsch synthesis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Light olens</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3379_431f32d512e5a75bb8d47dd92522fc94.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A New Three Parameter Cubic Equation of State</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3380</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Abdelrahman Rabah</LastName>
<Affiliation>Department of Chemistry,Kuwait University</Affiliation>

</Author>
<Author>
					<FirstName>Sumya</FirstName>
					<LastName>Abdel Moneim Mohamed</LastName>
<Affiliation>Department of Chemistry,Kuwait University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>A new three parameter Equation Of State (EOS) is developed based on well documented
data, at three thermodynamic states of the critical point, the normal bubble point and standard condition.
Besides these states, the EOS is designed to satisfy the condition of nearly zero Joule-Thomson (JT)
coecients at the normal boiling point. Critical properties and densities at the normal boiling point
and a standard condition of more than 100 pure 
uids were used. The new EOS is validated using
experimental data and eight (8) of the popular EOSs, namely, SRK, PR, LLS, HK, MNM, SW, PT and
ALS. The experimental data for pure 
uids include 331 data points of vapor pressure covering 12 
uids
and compressibility at the critical condition of 23 
uids. For mixtures, the data includes 129 PVT data
points of 12 reservoir 
uids [seven (7) of them are Sudanese crude oil considered for publication for the
rst time and ve (5) from literature]. The new EOS is found to be superior to the existing EOSs in
the prediction of PVT properties of mixtures with a grand average percent absolute deviation (AAPD) of
3.18%. It is also comparable to the existing EOSs in the prediction of vapor pressure despite the fact that
existing EOSs are developed based on vapor pressure data; the grand average AAPD is 2.0. In terms of
compressibility at the critical point with the exception of LLS, the new EOS yields better results than all
other EOSs considered in this work.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Equation of state</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Joule-Thomson coecient</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PVT data</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Sudanese reservoir uids</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3380_d7ab3636bd5b7c46399b2dde09707863.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effects of Rock Permeability on Capillary Imbibition Oil Recovery from Carbonate Cores</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3381</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>I.</FirstName>
					<LastName>Goodarznia</LastName>
<Affiliation>Department of Chemical and Petroleum Engineering,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>H.</FirstName>
					<LastName>Darvishi</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
<Author>
					<FirstName>F.</FirstName>
					<LastName>Esmaeilzadeh</LastName>
<Affiliation>Department of Chemistry,Sharif University of Technology</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>In order to investigate the feasibility and eects of core permeability on capillary imbibition
recoverable oil from carbonate cores, some laboratory tests were carried out at the EOR research
laboratories of Sharif University, Iran. Outcrop rocks with dierent permeabilities were taken away from a
recognized outcrop and used in these experiments. Special core analysis tests were run on two core samples
to nd out relative permeability and end point saturations. Wellhead separator oil and gas samples were
collected and recombined to a reservoir gas - oil ratio. A core 
ooding system with a capability of free and
forced imbibition testing was designed and installed. A number of free and forced imbibition tests with
dierent cores under reservoir conditions were conducted. The results of the tests revealed that capillary
imbibition is an almost fast process at laboratory scale and the higher permeable cores will imbibe more
easily. A good correlation could be obtained when the ratio of recovery factor to ultimate recovery factor
versus a denite function of time was plotted. From these experiments, it concluded that an up scaled
relation can be perceived for very low permeable cores, the testing of which may take too long.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Carbonate cores</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Gravity drainage</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Imbibition</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Capillary pressure</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Wettability</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3381_ed9d57f542bcc9b15a38b448b23baaad.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>17</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparison of Sol-Gel Methods for Washcoating Metallic Substrates</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">3382</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>J.</FirstName>
					<LastName>Towfighi</LastName>
<Affiliation>Department of Chemical Engineering,Tarbiat Modares University</Affiliation>

</Author>
<Author>
					<FirstName>Faranak</FirstName>
					<LastName>Akhlaghian</LastName>
<Affiliation>Department of Chemical Engineering,Tarbiat Modares University</Affiliation>

</Author>
<Author>
					<FirstName>A.</FirstName>
					<LastName>Mohajeri</LastName>
<Affiliation>Department of Chemical Engineering,Tarbiat Modares University</Affiliation>

</Author>
<Author>
					<FirstName>A.</FirstName>
					<LastName>Zamaniyan</LastName>
<Affiliation>Department of Chemical Engineering,Tarbiat Modares University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>01</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>FeCrAl foils were coated with alumina. Washcoating solutions were prepared using dierent
sol-gel methods. Method A uses an inorganic precursor of aluminum nitrate and a complexing agent
of Acetylactone, method B is a hot hydrolysis of aluminum alkoxide, and method C is a modication
of method B, by adding aluminum acetylacetonate. The last method, D, is a hydrolysis of aluminum
alkoxide at room temperature. Washcoating solutions were deposited on FeCrAl foils through dip coating.
Then, the coated foils were dried at 100C and calcined at 600C/3 for 2 hours. Ultrasound vibration
tests showed a good adhesion of washcoat layers. Characteristics of the washcoat layers were determined
by X-Ray Diraction (XRD), Scanning Electron Microscopy (SEM), Brunauer-Emmet-Telller (BET),
and Thermal Gravimetric Analysis (TGA) tests. Results of BET tests show that surface areas in sol-gel
methods are greater than those found in the suspension method, and the inorganic sol-gel method (method
A) has a lower surface area than those found in organic sol-gel methods.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Sol-gel</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Organic and inorganic precursor</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Washcoating</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Alumina</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Metallic Substrate</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3382_b9267f7f376594fcda7d67f8eebc56e9.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
