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	<title>Mind games manipulation idealogy &#187; Article Summary</title>
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	<description>Creativite stuff and mostly personal point of views</description>
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		<title>Caption of Hg(II) from acid aqueous solution by immersed poly(N-vinylimidazole)</title>
		<link>http://kelvins.org/index.php/archives/23</link>
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		<pubDate>Tue, 09 Oct 2007 01:09:18 +0000</pubDate>
		<dc:creator>Kelvin</dc:creator>
				<category><![CDATA[Article Summary]]></category>

		<guid isPermaLink="false">http://kelvins.org/?p=23</guid>
		<description><![CDATA[&#8220;Caption of Hg(II) from acid aqueous solution by immersed poly(N-vinylimidazole) hydrogel particles was studied as a function of pH, counterion, and cation concentration. Fitting parameters to several sorption isotherms have been determined. Their values depend mostly on pH and less, on temperature and counterion, and suggest a large affinity of imidazole groups in the gel [...]]]></description>
			<content:encoded><![CDATA[<p align="left"><strong>&#8220;Caption of Hg(II) from acid aqueous solution by immersed poly(N-vinylimidazole) hydrogel particles was studied as a function of pH, counterion, and cation concentration. Fitting parameters to several sorption isotherms have been determined. Their values depend mostly on pH and less, on temperature and counterion, and suggest a large affinity of imidazole groups in the gel and mercury cations. <u><em>Practically total removal (94.4%) of Hg(II) is achieved at pH = 2, with 10 g of dry gel per liter of solution</em>,</u><u><em> when cation concentration was as large as 15,000 ppm (0.075 M)</em></u>. Polymer protonation decreases about fourfold the cation affinity, supporting competitive protonation- complexation mechanisms. By its side, metal uptake decreases polymer protonation. Thermal stability of loaded gels decreases with respect to metal free hydrogels. Scanning electron micrographs reveal no changes in the gel morphology upon cation binding, but Tg increases significantly with the Hg(II) content of loaded gels and swelling decreases moderately, indicating the role of the cation as ionic crosslinker. Practically total elution of Hg(II) is achieved with 1 M HNO3 in consecutive loadingelution cycles.<br />
© 2000 John Wiley &amp; Sons, Inc. J Appl Polym Sci 79: 1467-1475, 2001&#8243;</strong></p>
<p align="left">&nbsp;</p>
<p align="left">By: M. J. MOLINA,1 M. R. GO´ MEZ-ANTO´ N,1 B. L. RIVAS,2 H. A. MATURANA,2 I. F. PIE´ROLA3</p>
<p align="left">Summary:<br />
Methods of removing heavy metal contamination has been proposed:<br />
Filtration, chemical precipitation, simple and chelation ion exchange, sorption, membrane system.</p>
<p>Search for polymer resins and hydrogels which have electron donor groups have the ability to bind to metal cations.</p>
<p align="left">The use of resin has been proposed in these methods:</p>
<ol>
<li>ion-exchange resins</li>
<li>polymer-enhanced ultra filtration</li>
<li>precipitation agents</li>
</ol>
<p>Why Hydrogel?<br />
One reason is that they do not transfer susbtance to the aqueous solution, and can be easily cleaned up indefinately.<br />
Hydrogel used <strong>poly(vinylimidazole) hydrogel</strong><br />
(similar to vinylimidazolium sulphobetaine except no sulphate group)<br />
<em>Could sulphate group induce antisceptic properties?</em></p>
<p>Swelling properties was measured:<br />
4.32g of water per gram of dry gel<br />
(gel made is weighted, mixed with water of x amount. Reweighted difference is minused)</p>
<p><strong>How they measured Hg(II) sorption</strong><br />
Preformed in batch with hydrogel particles suspended in aq solution.<br />
Effective concentration of 10g of dry polymer per 1L of solution.<br />
Equilibrium took 2 days at r.t (20 degrees C)<br />
Concluded that time-dependent retention measurements that 15min was sufficient to reach equilibrium.</p>
<p><em>Apparatus and Method</em><br />
Tg was determined.<br />
Thermal stability studied.<br />
SEM micrograph was determined via coating surface with gold.</p>
<p>Potentiometric measurement were performed to determine the degree of protonation α by expression:</p>
<p>α = (10(pH initial) &#8211; 10(pH final))/(Hydrogel effective concentration)</p>
<p>Hydrogel effective concentration was deteremined by loading experiements, Hydrogel effective concentration was 10g/L = 0.1M.</p>
<p>The hydrogel was synthesized by a radical crosslinking polymerization.</p>
<p>@ pH = 2 most effective with both sulfuric and hydrochloric acid.<br />
Added 15000ppm final about left 840ppm, 94.4% Asborbed</p>
<p>Experimental capacity of a resin is smaller than the calculated maximum capacity, because part of the ligands is not accessible to the metallic ions.</p>
<p>Describes models used and suggestions for why the models fit or do not fit.</p>
<p>Affinity of the imidazole group is studied and reported that it has a large affinity.</p>
<p><strong>Protons and Hg(II)/metal cation compete to be bound by the imidazole group</strong></p>
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		<title>Novel sulfobetaine-sulfonic acid-contained superswelling hydrogels</title>
		<link>http://kelvins.org/index.php/archives/21</link>
		<comments>http://kelvins.org/index.php/archives/21#comments</comments>
		<pubDate>Thu, 04 Oct 2007 02:43:19 +0000</pubDate>
		<dc:creator>Kelvin</dc:creator>
				<category><![CDATA[Article Summary]]></category>

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		<description><![CDATA[&#8220;Novel hydrogels based on zwitterionic monomer [3-(methacrylamido)propyl] dimethyl (3-sulfopropyl)
ammonium hydroxide (MPDSAH) and a strong acid monomer (2-acrylamido-2-methylpropane
sulfonic acid, AMPS) were synthesized through solution polymerization under normal conditions
to achieve nearly quantitative gel yield. The structure of the gels was confirmed using infrared
spectroscopy. Thermal properties were simultaneously studied by differential scanning calorimetry
and thermogravimetric analysis (DSC/TGA). The effects [...]]]></description>
			<content:encoded><![CDATA[<p align="left"><strong>&#8220;Novel hydrogels based on zwitterionic monomer [3-(methacrylamido)propyl] dimethyl (3-sulfopropyl)<br />
ammonium hydroxide (MPDSAH) and a strong acid monomer (2-acrylamido-2-methylpropane<br />
sulfonic acid, AMPS) were synthesized through solution polymerization under normal conditions<br />
to achieve nearly quantitative gel yield. The structure of the gels was confirmed using infrared<br />
spectroscopy. Thermal properties were simultaneously studied by differential scanning calorimetry<br />
and thermogravimetric analysis (DSC/TGA). The effects of the polymerization variables on the<br />
swelling capacity of the products were investigated. It was found that, in a certain range of the<br />
monomers mol ratio, increase of AMPS content was surprisingly accompanied with swelling reduction.<br />
The swelling exhibited lower sensitivity to the crosslinker concentration (range 0.6-1.2 wt%)<br />
compared with the conventional superabsorbents. However, in contrast with the conventional<br />
acrylic acid-based superabsorbents, the neutralization degree of AMPS part of the new gels had<br />
only a small enhancing effect on their swelling capacity. The effect of total monomer concentration<br />
on the hydrogel absorbency was also studied. The fully ionic hydrogels showed an unusual pHindependency<br />
behavior, so that their absorbency was nearly unchanged in a wide range of pH.<br />
Such unexpected behavior was also observed for the swelling in the ionic environments with various<br />
ionic strengths. Copyright # 2005 John Wiley &amp; Sons, Ltd.&#8221;</strong></p>
<p align="left">&nbsp;</p>
<p align="left">&nbsp;</p>
<p align="left">By:<br />
Kourosh Kabiri 1, Sara Faraji-Dana 2 3, Mohammad J. Zohuriaan-Mehr 1 *<br />
1Superabsorbent Hydrogel Division, Department of Paint, Resin and Surface Coatings, Iran Polymer and Petrochemical Institute (IPPI), P. O. Box 14965-115, Tehran, Iran<br />
2Department of Chemistry, Sharif University of Technology, P.O. Box 11365-9516, Tehran, Iran<br />
3R&amp;D Division, Rahab Resin Co., P.O. Box 14185-458, Tehran, Iran</p>
<p align="left">&nbsp;</p>
<p align="left">&nbsp;</p>
<p align="left">email: Mohammad J. Zohuriaan-Mehr (m.zohuriaan@ippi.ac.ir mjzohuriaan@yahoo.com)</p>
<p>*Correspondence to Mohammad J. Zohuriaan-Mehr, Superabsorbent Hydrogel Division, Department of Paint, Resin and Surface Coatings, Iran Polymer and Petrochemical Institute (IPPI), P. O. Box 14965-115, Tehran, Iran.</p>
<p align="left">&nbsp;</p>
<p align="left">&nbsp;</p>
<p align="left">Summary:<br />
Super swelling due to cross linked hydrophphilic structure. Conventially it is though that superabsobents are preapred from non-ioni-anionic monomers.</p>
<p align="left">&nbsp;</p>
<p align="left">The water absorbance is usually decreased substantially when the gel is put into an ionic medium. <em>However some lightly crosslinked amphoteric polyelectrolytes and polyzwitterions have potential to swell more in salt solution than in pure water.</em></p>
<p align="left">&nbsp;</p>
<p align="left">(i.e from 1-vinyl-3-sulfopropylimidazolium hydroxide inner salt imbibe 91% of 1M NaCl. whilst in deionised water gel absorbed only 46%)</p>
<p align="left">&nbsp;</p>
<p align="left">With a breif review of literature hydrogels, sulfobetaines are exnteisvely used in industries with textiles, adhesives, coatings, flocculants</p>
<p align="left">AMPS and like derivatives where the monomer 2-acrylamido-2-methylpropanesulfonic acid is copolymerized with other conventional arcylic monomers creating a hydrogel. ( acrylic acid, acrylamide, N,N-dimethylacrylamide and n-dodecyl poly(oxyethylene) maleate)</p>
<p align="left">Suggested used of AMPS with acrylic monomer are skin contact electrodes, support carrier in biomedical engineering and drug delivery applications.</p>
<p align="left">AMP mixed with copolmer to create superabsorbent hydrogels.</p>
<p>Literature has no dictated polymers of sulfobetaine-type monomer and AMPS.</p>
<p><strong>Variables affecting swelling</strong><br />
<em>comonomer ratio</em><br />
<em> crosslinker content<br />
total monomer concentration<br />
neutralization degree of AMPs on swelling behaviour of the gels which have been investigated</em></p>
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