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	<title>Esstech News &#124; Esstech Blog &#124; Specialty Chemicals Resources</title>
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		<title>New Additions to the Esstech Team</title>
		<link>http://esstechinc.com/blog/new-additions-to-the-esstech-team/</link>
		<comments>http://esstechinc.com/blog/new-additions-to-the-esstech-team/#comments</comments>
		<pubDate>Wed, 11 Jan 2012 15:29:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Announcements]]></category>
		<category><![CDATA[adhesives]]></category>
		<category><![CDATA[coatins]]></category>
		<category><![CDATA[dental research]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[oligomers]]></category>
		<category><![CDATA[Photopolymers]]></category>
		<category><![CDATA[steriolithography]]></category>
		<category><![CDATA[UV Curable]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=593</guid>
		<description><![CDATA[From its simple origins in the early 1990&#8242;s as a line of highly customized raw materials for compounders of &#8220;new generation&#8221; restorative dental composites to now a major manufacturer of customized UV/EB curable materials serving an ever-wider range of industries, Esstech, Inc. has indeed been a very successful &#8220;experiment&#8221;.  It is my pleasure to announce [...]]]></description>
			<content:encoded><![CDATA[<p><em><span style="color: #000080;">From its simple origins in the early  1990&#8242;s as a line of highly customized raw materials for compounders of  &#8220;new generation&#8221; restorative dental composites to now a major  manufacturer of customized UV/EB curable materials serving an ever-wider  range of industries, Esstech, Inc. has indeed been a very successful  &#8220;experiment&#8221;.  It is my pleasure to announce two additions to the  Esstech Team of talented professionals.<br />
 </span></em></p>
<p><em><br />
 <span style="color: #000080;">Last year,</span> <a href="mailto:bruce.farina@esstechinc.com?subject=Esstech%20Inquiry"><strong>Bruce Farina</strong></a><span style="color: #000080;">,  a 21-year veteran of Sartomer Company, joined Esstech as Senior Vice  President and we are now pleased to announce that, effective as of  January 1, 2012, Bruce has been given full operational responsibility  for Esstech as President/COO.  Bruce&#8217;s two decades of experience at  Sartomer ranged from Manufacturing Manager through various titles and  functions to Vice President with, most recently, overall global  responsibility for all of Sartomer&#8217;s photocure (UV/EB) business. </span><br />
 </em></p>
<p><em><br />
 <span style="color: #000080;">Bruce is taking over for </span><a href="mailto:howard.slaff@esschem.com?subject=Esschem%20Inquiry"><strong>Howard Slaff</strong></a> <span style="color: #000080;">who, after a very successful leadership tenure at Esstech, is moving  ten miles south down I-95 to assume the President/COO responsibilities  being vacated by the retiring Mike Norquist at Esstech&#8217;s sister company,  Esschem, Inc.. </span><br />
 </em></p>
<p><em><br />
 <span style="color: #000080;">I am also very pleased to announce that Bruce has successfully recruited </span><a href="mailto:mike.idacavage@esstechinc.com?subject=Esstech%20Inquiry"><strong>Dr. Mike Idacavage</strong></a> <span style="color: #000080;">as Esstech&#8217;s new Director of Business Development.  Mike Idacavage may  be known to some of you as the immediate past-President of RadTech North  America and is a lifetime member of RadTech&#8217;s Board of Directors.   Mike&#8217;s &#8220;day job&#8221; for the last 15 years was with Cytec Industries (and,  pre-merger, UCB Chemicals), most recently as Cytec&#8217;s Principal Research  Fellow.<br />
 </span></em></p>
<p><em><span style="color: #000080;"><br />
 Those of us involved with Esstech over the years could not be more  excited with the Team now in place and with their commitment to its next  phase of customer-centric growth! </span></em><span style="color: #000080;"><br />
<em> <br />
 Please check us out at <a href="http://us1.campaign-archive2.com/www.esstechinc.com">www.esstechinc.com</a> !</p>
<p> <span style="color: #000080;">Henry M. (&#8220;Tac&#8221;) Justi<br />
 Chairman</span></em></span></p>
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		<title>TPO Evaluated in Dental Composites</title>
		<link>http://esstechinc.com/blog/tpo-evaluated-in-dental-composites/</link>
		<comments>http://esstechinc.com/blog/tpo-evaluated-in-dental-composites/#comments</comments>
		<pubDate>Mon, 09 Jan 2012 17:42:05 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Research Paper]]></category>
		<category><![CDATA[bis-GMA]]></category>
		<category><![CDATA[bisGMA]]></category>
		<category><![CDATA[camphorquinone]]></category>
		<category><![CDATA[composite]]></category>
		<category><![CDATA[conversion]]></category>
		<category><![CDATA[dental research]]></category>
		<category><![CDATA[TEGDMA]]></category>
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		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=541</guid>
		<description><![CDATA[Curing efficiency of dental resin composites formulated with camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide Luis Felipe J. Schneider, Larissa Maria Cavalcante, Scott A. Prah, Carmem S. Pfeifer, Jack L. Ferracane.  &#8220;Curing efficiency of dental resin composites formulated with camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide&#8221; Dental Materials.  December 2011:  Online Summary: This research presents trimethylbenzoyl-diphenyl-phosphine oxide (TPO) as an alternative [...]]]></description>
			<content:encoded><![CDATA[<h1>Curing efficiency of dental resin composites formulated with camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide</h1>
<p>Luis Felipe J. Schneider, Larissa Maria Cavalcante, Scott A. Prah, Carmem S. Pfeifer, Jack L. Ferracane.  &#8220;Curing efficiency of dental resin composites formulated with camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide&#8221; <em>Dental Materials</em>.  December 2011:  Online</p>
<ul>
</ul>
<div>
<h4 id="absSec_N4a9404d8N7ae044e0">Summary:</h4>
<p id="spar0005">This research presents trimethylbenzoyl-diphenyl-phosphine oxide  (TPO) as an alternative to camphorquinone (CQ)  photoinitiator systems for dental resins.  An immediate advantage is the low color of TPO in comparison to the strong yellow color of CQ. Testing using a spectrophotometer and differential scanning calorimetry (DSC) revealed that TPO had higher reactivity than CQ.  CQ exhibited higher absorbed power density, (PD<sub>abs</sub>) and better depth of cure.</p>
<h4 id="absSec_N4a9404d8N7ae04540">Materials</h4>
<p id="spar0010">Testing of each photoinitiator was performed using 50:50 formulations of 2,2-bis[4-2(2-hydroxy-3-<br />
 methacroyloxypropoxy)phenyl]propane (<a href="http://esstechinc.thomasnet.com/item/resins/bisgma/x-950-0000?&amp;forward=1" target="_blank">Bis-GMA</a>, <strong>Esstech</strong>) and triethyleneglycol dimethacrylate (<a href="http://esstechinc.thomasnet-navigator.com/viewitems/difunctional-monomers/triethyleneglycol-dimethacrylate?&amp;forward=1">TEGDMA</a>, <strong>Esstech</strong>).</p>
</div>
<p><br class="spacer_" /></p>
<p>LINK:  <a href="http://dx.doi.org/10.1016/j.dental.2011.11.014" target="_blank">http://dx.doi.org/10.1016/j.dental.2011.11.014</a></p>
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		<title>Esstech Attending CIOSP 2012</title>
		<link>http://esstechinc.com/blog/esstech-attending-ciosp-2012/</link>
		<comments>http://esstechinc.com/blog/esstech-attending-ciosp-2012/#comments</comments>
		<pubDate>Mon, 05 Dec 2011 17:31:13 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Announcements]]></category>
		<category><![CDATA[dental research]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[tradeshow]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=550</guid>
		<description><![CDATA[Join us in Sau Paulo for the CIOSP dental show, January 28-31. We are planning a very exciting and busy trip so contact us immediately to schedule a meeting. Hope to see you there! Phone:  1-800-245-3800 or 610-521-3800 EMail:  techsupport@esstechinc.com.  EXOTHANE™ Elastomers · Adhesive Monomers · Dental Resins]]></description>
			<content:encoded><![CDATA[<p><br class="spacer_" /></p>
<p style="text-align: center;"><a href="http://www.ciosp.com.br/" target="_blank"><img class="size-full wp-image-559 aligncenter" title="CIOSP logo_header_middle_logo_event" src="http://www.esstechinc.com/blog/wp-content/uploads/CIOSP-logo_header_middle_logo_event.jpg" alt="" width="307" height="114" /></a></p>
<p style="text-align: center;"><strong>Join us in Sau Paulo for the CIOSP dental show, January 28-31.</strong></p>
<p style="text-align: center;"><strong>We are planning a very exciting and busy trip so contact us immediately to schedule a meeting.</strong></p>
<p style="text-align: center;"><strong>Hope to see you there!</strong></p>
<p style="text-align: center;"><strong><br />
 </strong></p>
<div style="text-align: center;">Phone:  1-800-245-3800 or 610-521-3800<br />
 EMail:  <a href="mailto:techsupport@esstechinc.com?subject=Improved%20PMGDM%20Adhesive%20Monomer">techsupport@esstechinc.com</a>. <br />
 <a href="mailto:techsupport@esstechinc.com?subject=Esstech%27s%20Monthly%20Email%20Update"><img src="https://d2q0qd5iz04n9u.cloudfront.net/_ssl/proxy.php/http/gallery.mailchimp.com/e6d67d97266b9e2da6fdc57ac/images/iconEmail.gif" border="0" alt="Email" width="44" height="50" /></a> <a href="../index.php/feed/" target="_blank"><img src="https://d2q0qd5iz04n9u.cloudfront.net/_ssl/proxy.php/http/gallery.mailchimp.com/e6d67d97266b9e2da6fdc57ac/images/iconRSS.gif" border="0" alt="" width="44" height="50" /></a> <a href="http://twitter.com/home?status=Esstech%27s+Monthly+Email+Update+-+http%3A%2F%2Feepurl.com%2FD7P3" target="_blank"><img src="https://d2q0qd5iz04n9u.cloudfront.net/_ssl/proxy.php/http/gallery.mailchimp.com/e6d67d97266b9e2da6fdc57ac/images/twitter_logo.png" border="0" alt="" width="46" height="46" /></a> <a href="http://www.facebook.com/share.php?u=http%3A%2F%2Fus1.campaign-archive.com%2F%3Fu%3De6d67d97266b9e2da6fdc57ac%26id%3D8806842bdb&amp;t=Esstech%27s+Monthly+Email+Update" target="_blank"><img src="https://d2q0qd5iz04n9u.cloudfront.net/_ssl/proxy.php/http/gallery.mailchimp.com/e6d67d97266b9e2da6fdc57ac/images/FaceBook_64x64.png" border="0" alt="" width="46" height="46" /></a> <a href="http://www.linkedin.com/shareArticle?mini=true&amp;url=http%3A%2F%2Fus1.campaign-archive.com%2F%3Fu%3De6d67d97266b9e2da6fdc57ac%26id%3D8806842bdb&amp;title=Esstech%27s+Monthly+Email+Update" target="_blank"><img src="https://d2q0qd5iz04n9u.cloudfront.net/_ssl/proxy.php/http/gallery.mailchimp.com/e6d67d97266b9e2da6fdc57ac/images/iconLinkedin.1.gif" border="0" alt="" width="44" height="50" /></a></div>
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		<title>Optimized LED cure of BisGMA:TEGDMA</title>
		<link>http://esstechinc.com/blog/optimized-led-cure-of-bisgmategdma/</link>
		<comments>http://esstechinc.com/blog/optimized-led-cure-of-bisgmategdma/#comments</comments>
		<pubDate>Thu, 01 Dec 2011 20:22:18 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Research Paper]]></category>
		<category><![CDATA[bisGMA]]></category>
		<category><![CDATA[CQ]]></category>
		<category><![CDATA[dental research]]></category>
		<category><![CDATA[TEGDMA]]></category>
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		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=546</guid>
		<description><![CDATA[Micro-Raman spectroscopic analysis of the degree of conversion of composite resins containing different initiators cured by polywave or monowave LED units Vesna Miletic a, Ario Santini b, a Clinical Lecturer, University of Belgrade, School of Dentistry, Department of Restorative Odontology and Endodontics, Rankeova 4, Belgrade, Serbia b Director of Biomaterials Research, The University of Edinburgh, [...]]]></description>
			<content:encoded><![CDATA[<div>
<h3>Micro-Raman spectroscopic  analysis of the degree of conversion of composite resins containing  different initiators cured by polywave or monowave LED units</h3>
</div>
<p style="padding-left: 30px;">Vesna Miletic<sup> a</sup>, Ario Santini<sup> b</sup>,</p>
<p style="padding-left: 30px;"><sup>a</sup> Clinical Lecturer, University of Belgrade, School of Dentistry, Department of Restorative Odontology and Endodontics, Rankeova 4, Belgrade, Serbia</p>
<p style="padding-left: 30px;"><sup>b</sup> Director of Biomaterials Research, The University of Edinburgh, Edinburgh Postgraduate Dental Institute, Lauriston Place, Edinburgh EH3 9HA, United Kingdom</p>
<p style="padding-left: 30px;">Received 20 August 2011; revised 28 October 2011; Accepted 30 October 2011. Available online 6 November 2011.</p>
<div>
<div>
<div>
<h4>Objectives</h4>
<p id="spar0005">To  determine the degree of conversion (DC) over 48 h post-curing of resin  mixtures containing trimethylbenzoyl-diphenylphosphine oxide (TPO)  initiator cured by a polywave or a monowave LED light-curing unit (LCU).</p>
<h4>Methods</h4>
<p id="spar0010">In  resin mixtures based on equal weight percent (wt%) of <a href="http://esstechinc.thomasnet.com/item/resins/bisgma/x-950-0000?&amp;forward=1" target="_blank">BisGMA</a> and <a href="http://esstechinc.thomasnet-navigator.com/viewitems/difunctional-monomers/triethyleneglycol-dimethacrylate?&amp;forward=1" target="_blank">TEGDMA</a> the following initiators were added: 0.2wt% camphorquinone (CQ) +  0.8wt% ethyl-4-dimethylaminobenzoate (EDMAB) (Group 1); 1wt% TPO (Group  2) and 0.1wt% CQ + 0.4wt% EDMAB + 0.5wt% TPO (Group 3). Half of the  samples in each group (n = 5) were cured using a polywave (bluephase<sup>®</sup> G2, Ivoclar Vivadent) or a monowave LED LCU (bluephase<sup>®</sup>,  Ivoclar Vivadent). The DC was measured using micro-Raman spectroscopy  within 5 min and then 1, 3, 6, 24 and 48 h post-irradiation. The data  were analyzed using general linear model and two-way ANOVA for the  factors ‘time’, ‘material’, ‘surface’ and ‘LCU’ at α=0.05.</p>
<h4>Results</h4>
<p id="spar0015">The initial DC values obtained upon light curing remained similar over a 48 h period. bluephase<sup>®</sup> G2 produced the highest DC in Group 2 followed by Group 3, and Group 1. bluephase<sup>®</sup> resulted in the highest DC in Group 1, followed by Group 2 and Group 3 (p &lt; 0.05).</p>
<h4>Conclusions</h4>
<p id="spar0020">Unfilled resin materials containing both TPO- and CQ-amine initiators are effectively cured using bluephase<sup>®</sup> G2. Resin mixture with the same wt% of initiators is better cured when  TPO is the only initiator, compared to CQ-amine only or combined TPO and  CQ-amine system. After initial light cure, no additional conversion of  uncured monomers was detected in an unfilled resin material over 48 h at  37 °C.</p>
</div>
</div>
</div>
<h4>Materials</h4>
<p><strong>&#8230;</strong> Page 5 of 24 Ac ce pte d M an usc rip t 4 Materials and Methods The following materials were<br />
 used in the study: <a href="http://esstechinc.thomasnet.com/item/resins/bisgma/x-950-0000?&amp;forward=1" target="_blank">bisphenol A bis(2-bydroxy-3- methacryloxypropyl)ether (BisGMA)</a>,<a href="http://esstechinc.thomasnet-navigator.com/viewitems/difunctional-monomers/triethyleneglycol-dimethacrylate?&amp;forward=1" target="_blank"> triethylene<br />
 glycol dimethacrylate (TEGDMA)</a>, camphorquinone (CQ) (<strong>Esstech</strong> Inc, Essington, PA <strong>&#8230;</strong></p>
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		<title>LOW SHRINK, HIGH CONVERSION</title>
		<link>http://esstechinc.com/blog/low-shrink-high-conversion/</link>
		<comments>http://esstechinc.com/blog/low-shrink-high-conversion/#comments</comments>
		<pubDate>Fri, 11 Nov 2011 23:08:46 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Announcements]]></category>
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		<category><![CDATA[esstech]]></category>
		<category><![CDATA[EXOTHANE]]></category>
		<category><![CDATA[EXOTHANE Elastomers]]></category>
		<category><![CDATA[High conversion]]></category>
		<category><![CDATA[low shrinkage stress]]></category>
		<category><![CDATA[low volumetric shrinkage]]></category>
		<category><![CDATA[Monomer]]></category>
		<category><![CDATA[polymerization]]></category>
		<category><![CDATA[Resin]]></category>
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		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=517</guid>
		<description><![CDATA[Do not sacrifice conversion and the risk of residual monomer contamination to achieve low-shrink properties.  New testing has demonstrated that EXOTHANE(TM) Elastomers have low shrinkage stress, low volumetric shrinkage, AND high conversion. Exothane 8, 94% Conversion, 3% Shrinkage, high % elongation Exothane 26, 96% Conversion, 4% Shrinkage, increased flexibility/toughness Exothane 32, 97% Conversion, 3% Shrinkage, [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center;"><a href="http://esstechinc.thomasnet.com/viewitems/all-categories/esstech-specialty-chemicals-exothane" target="_blank"><img class="size-full wp-image-518 aligncenter" title="GIFlogoColorLarge" src="http://www.esstechinc.com/blog/wp-content/uploads/GIFlogoColorLarge.gif" alt="EXOTHANE Elastomers" width="350" height="211" /></a></p>
<p>Do not sacrifice conversion and the risk of residual monomer contamination to achieve low-shrink properties.  New testing has demonstrated that <a href="http://esstechinc.thomasnet.com/viewitems/all-categories/esstech-specialty-chemicals-exothane" target="_blank">EXOTHANE(TM) Elastomers</a> have low shrinkage stress, low volumetric shrinkage, AND high conversion.</p>
<ul>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/x-891-0000-2?&amp;bc=0%7C1101" target="_blank">Exothane 8</a>, 94% Conversion, 3% Shrinkage, high % elongation</li>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/x-892-0000-2?&amp;bc=0%7C1101" target="_blank">Exothane 26</a>, 96% Conversion, 4% Shrinkage, increased flexibility/toughness</li>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/exothane-32?&amp;bc=0%7C1101" target="_blank">Exothane 32</a>, 97% Conversion, 3% Shrinkage, low color and low viscosity</li>
</ul>
<p>This new data, in addition to superior toughness, tensilse strength and percent elongation make the EXOTHANE product line ideal form many applications including, low-shrink dental restoratives, non-curling industrial coatings, unique UV nail enhancements, tougher anaerobic adhesives and more.</p>
<p><br class="spacer_" /></p>
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		<title>PRODUCT SPOTLIGHT:  HEMA Maleate</title>
		<link>http://esstechinc.com/blog/product-spotlight-hema-maleate/</link>
		<comments>http://esstechinc.com/blog/product-spotlight-hema-maleate/#comments</comments>
		<pubDate>Fri, 11 Nov 2011 19:08:28 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Adhesive Monomer]]></category>
		<category><![CDATA[diluent]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[Monofunctional]]></category>
		<category><![CDATA[Monomer]]></category>
		<category><![CDATA[X-846-0000]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=458</guid>
		<description><![CDATA[Item Code: X-846-0000 Product Name: Methacryloyloxyethyl Maleate CAS#: 51978-15-5 EINECS(I): 257-569-5 INCI: HEMA Maleate HEMA maleate is a carboxylic acid-containing methacrylate that can function as an alternative to PMDM. It has been used in anaerobic adhesive applications and is approved for use in cosmetic products. The carboxylic acid group of X-846-0000 has the ability to [...]]]></description>
			<content:encoded><![CDATA[<p><strong>Item Code:</strong><a href="http://esstechinc.thomasnet.com/item/adhesive-monomers/methacroyloxyethyl-maleate/x-846-0000?" target="_blank"></a><a href="http://esstechinc.thomasnet.com/item/adhesive-monomers/methacroyloxyethyl-maleate/x-846-0000?" target="_blank"> X-846-0000</a><img class="size-full wp-image-528 alignright" title="HEMA Maleate" src="http://www.esstechinc.com/blog/wp-content/uploads/a1012.jpg" alt="X-846-0000, HEMA Maleate" width="315" height="120" /></p>
<p><strong>Product Name: </strong> Methacryloyloxyethyl Maleate<br />
 <strong>CAS#:</strong> 51978-15-5</p>
<p><strong>EINECS(I):</strong> 257-569-5<br />
 <strong>INCI:</strong> HEMA Maleate</p>
<p>HEMA maleate is a carboxylic acid-containing methacrylate that can function as an alternative to <a href="http://esstechinc.thomasnet.com/item/adhesive-monomers/adhesive-monomer-pmdm/x-865-0000?" target="_blank">PMDM</a>. It has been used in anaerobic adhesive applications and is approved for use in cosmetic products.</p>
<p>The carboxylic acid group of <a href="http://esstechinc.thomasnet.com/item/adhesive-monomers/methacroyloxyethyl-maleate/x-846-0000?" target="_blank">X-846-0000</a> has the ability to improve adhesion to keratin.  Its’ monomethacrylate functionality allows it to be incorporated into soak-off systems without detriment to “removability”.  HEMA maleate’s low viscosity also makes it an ideal, reactive diluents.</p>
<p>Contact us directly to discuss your application and request samples, <a href="mailto:techsupport@esstechinc.com">techsupport@esstechinc.com</a>.</p>
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		<title>Urethane Dimethacrylate used in Rapid Prototyping Application</title>
		<link>http://esstechinc.com/blog/urethane-dimethacrylate-used-in-rapid-prototyping-application/</link>
		<comments>http://esstechinc.com/blog/urethane-dimethacrylate-used-in-rapid-prototyping-application/#comments</comments>
		<pubDate>Thu, 13 Oct 2011 17:27:33 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Research Paper]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[lithography]]></category>
		<category><![CDATA[nanocomposite]]></category>
		<category><![CDATA[rapid prototyping]]></category>
		<category><![CDATA[UDMA]]></category>
		<category><![CDATA[urethane]]></category>
		<category><![CDATA[X-850-0000]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=506</guid>
		<description><![CDATA[Characterization of a nanoparticle-filled resin for application in scan-LED-technology Eva Kolb, Claudia Kummerlöwe and Martin Klare Journal of Materials Science: Materials in Medicine Volume 22, Number 10, 2165-2173, DOI: 10.1007/s10856-011-4411-7 Abstract Scan-LED-technology is a new rapid prototyping technique with increasing applications in the production of custom-made medical products. The present work is dealing with the [...]]]></description>
			<content:encoded><![CDATA[<div>
<h1>Characterization of a nanoparticle-filled resin for application in scan-LED-technology</h1>
<p><a title="View content where Author is Eva Kolb" href="http://www.springerlink.com/content/?Author=Eva+Kolb">Eva Kolb</a>, <a title="View content where Author is Claudia Kummerlöwe" href="http://www.springerlink.com/content/?Author=Claudia+Kummerl%c3%b6we">Claudia Kummerlöwe</a> and <a title="View content where Author is Martin Klare" href="http://www.springerlink.com/content/?Author=Martin+Klare">Martin Klare</a></p>
<div>
<div><a title="Link to the Journal of this Article" lang="en" href="http://www.springerlink.com/content/0957-4530/">Journal of Materials Science: Materials in Medicine</a></div>
<div><a title="Link to the Issue of this Article" lang="en" href="http://www.springerlink.com/content/0957-4530/22/10/">Volume 22, Number 10</a>, 2165-2173, DOI: 10.1007/s10856-011-4411-7</div>
<div>
<h2>Abstract</h2>
<div>
<div lang="en">
<div>Scan-LED-technology  is a new rapid prototyping technique with increasing applications in  the production of custom-made medical             products. The present work is dealing with the examination  of a silica/<a href="http://esstechinc.thomasnet.com/item/resins/urethane-dimethacrylate/x-850-0000?&amp;forward=1" target="_blank">urethandimethacrylate (UDMA)</a> nanocomposite for application             in scan-LED-technology. The use of specific LED in a  photo-DSC unit enables the simulation of crucial parameters of  nanoparticle-filled             resins for their application in scan-LED-technology. The  conversion of double bonds during the curing reaction and the rate             of conversion were studied as a function of radiation  intensity, silica nanoparticle content, and silanization of the  nanoparticles             with 3-methacryloyloxypropyl-trimethoxysilane (MPTMS). The  conversion of double bonds is increasing with increasing radiation             intensity. The increasing conversion of the  nanoparticle-filled resins is discussed as a combined effect of  increasing nanoparticle             content, alternated initiator/double bond ratio and  increasing radiation intensity. A significant dependence of the reaction             rate on nanoparticle content could not be found. Only for  the unfilled resin, the rate was increasing at higher radiation             intensities. The influence of residual solvent on conversion  and rate of reaction was also analyzed. TGA measurements combined             with FTIR were used to study the silanization of the  nanoparticles. The silane layer thickness on the surface of the silica             nanoparticles was determined.</div>
<div>-</div>
<div>LINK:  <a href="http://www.springerlink.com/content/e474308303034537/" target="_blank">http://www.springerlink.com/content/e474308303034537/</a></div>
<div>-</div>
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		<title>Introducing EXOTHANE Elastomers</title>
		<link>http://esstechinc.com/blog/introducing-exothane-elastomers/</link>
		<comments>http://esstechinc.com/blog/introducing-exothane-elastomers/#comments</comments>
		<pubDate>Wed, 28 Sep 2011 13:48:26 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Announcements]]></category>
		<category><![CDATA[composite]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[EXOTHANE]]></category>
		<category><![CDATA[low-shrink]]></category>
		<category><![CDATA[Monomer]]></category>
		<category><![CDATA[urethane]]></category>
		<category><![CDATA[X-726-0000]]></category>
		<category><![CDATA[X-850-0000]]></category>
		<category><![CDATA[X-891-0000]]></category>
		<category><![CDATA[X-892-0000]]></category>
		<category><![CDATA[X-893-0000]]></category>
		<category><![CDATA[X-894-0000]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=478</guid>
		<description><![CDATA[Optimize Photocurable Mechanical Properties EXOTHANE™ Elastomers represent the most recent advances in Esstech&#8217;s urethane chemistry. These versatile materials offer performance enhancements across a broad range of demanding formulations. Exothane 8, low color urethane, creates a &#8220;soft&#8221; yet tough polymer with high elongation Exothane 26, high flexibility when cured, has the ability to re-adhere at lower [...]]]></description>
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<h2><a href="http://esstechinc.thomasnet.com/viewitems/all-categories/esstech-specialty-chemicals-exothane?" target="_blank"><img class="aligncenter size-full wp-image-481" style="border: 0pt none;" title="JPGlogoColorLarge" src="http://www.esstechinc.com/blog/wp-content/uploads/JPGlogoColorLarge.jpg" alt="EXOTHANE Elastomers" width="350" height="211" /></a></h2>
<h2>Optimize   Photocurable Mechanical Properties</h2>
<p><a href="http://esstechinc.thomasnet.com/viewitems/all-categories/esstech-specialty-chemicals-exothane?" target="_blank">EXOTHANE™ Elastomers</a> represent the most recent advances in Esstech&#8217;s urethane   chemistry.  These versatile materials   offer performance enhancements across a broad range of demanding   formulations.</p>
<ul>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/x-891-0000-2?&amp;bc=0|1101" target="_blank">Exothane 8</a>, low color urethane, creates a &#8220;soft&#8221; yet tough        polymer with high elongation</li>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/x-892-0000-2?&amp;bc=0|1101" target="_blank">Exothane 26</a>, high flexibility when cured, has the ability to        re-adhere at lower tensile strength</li>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/exothane-24?&amp;bc=0|1101" target="_blank">Exothane 24</a>, high crosslink capacity, low in color and viscosity        and very high Shore D hardness</li>
<li><a href="http://esstechinc.thomasnet.com/item/all-categories/esstech-specialty-chemicals-exothane/exothane-32?&amp;bc=0|1101" target="_blank">Exothane 32</a>, very low in color and viscosity, provides improved        flexibility</li>
</ul>
<p>Like many of Esstech&#8217;s other products, potential applications   involving EXOTHANE™ Elastomers can vary across many industries from medical   devices and nail gel enhancements to radiation-curable coatings.</p>
<p>Contact us directly to discuss <span style="text-decoration: underline;">your</span> unique requirements and request our EXOTHANE™ Elastomers Product   Literature.</p>
<p>Phone:  1-800-245-3800 or 610-521-3800<br />
 EMail:  <a href="mailto:techsupport@esstechinc.com?subject=Improved%20PMGDM%20Adhesive%20Monomer">techsupport@esstechinc.com</a>. <br />
 <a href="mailto:techsupport@esstechinc.com?subject=Esstech%27s%20Monthly%20Email%20Update"></a> <a href="../../../../../index.php/feed/?utm_source=All+Contacts&amp;utm_campaign=9113fa466d-EXOTHANE_Introduction9_2_2011&amp;utm_medium=email" target="_blank"></a> <a href="http://twitter.com/home?status=Esstech%27s+Monthly+Email+Update+-+http://eepurl.com/D7P3&amp;utm_source=All+Contacts&amp;utm_campaign=9113fa466d-EXOTHANE_Introduction9_2_2011&amp;utm_medium=email" target="_blank"></a> <a href="http://www.facebook.com/share.php?u=http://us1.campaign-archive.com/?u=e6d67d97266b9e2da6fdc57ac&amp;id=8806842bdb&amp;t=Esstech%27s+Monthly+Email+Update&amp;utm_source=All+Contacts&amp;utm_campaign=9113fa466d-EXOTHANE_Introduction9_2_2011&amp;utm_medium=email" target="_blank"></a> <a href="http://www.linkedin.com/shareArticle?mini=true&amp;url=http://us1.campaign-archive.com/?u=e6d67d97266b9e2da6fdc57ac&amp;id=8806842bdb&amp;title=Esstech%27s+Monthly+Email+Update&amp;utm_source=All+Contacts&amp;utm_campaign=9113fa466d-EXOTHANE_Introduction9_2_2011&amp;utm_medium=email" target="_blank"></a></p>
<p>Esstech products are available to our   European customers via, Esschem Europe</p>
<p>(<a href="http://www.esschem-europe.com/?utm_source=All+Contacts&amp;utm_campaign=9113fa466d-EXOTHANE_Introduction9_2_2011&amp;utm_medium=email" target="_blank">www.esschem-europe.com</a>).</p>
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		<title>Esstech Attending UV.EB East</title>
		<link>http://esstechinc.com/blog/esstech-attending-uv-eb-east/</link>
		<comments>http://esstechinc.com/blog/esstech-attending-uv-eb-east/#comments</comments>
		<pubDate>Wed, 21 Sep 2011 17:39:21 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Announcements]]></category>
		<category><![CDATA[esstech]]></category>
		<category><![CDATA[EXOTHANE Elastomers]]></category>
		<category><![CDATA[Monomer]]></category>
		<category><![CDATA[Radiation Curable]]></category>
		<category><![CDATA[tradeshow]]></category>
		<category><![CDATA[UV Curable]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=489</guid>
		<description><![CDATA[Esstech will be attending the UV.EB East Show in Syracuse, NY from October 4th to the 5th. We look forward to seeing everyone, making appointments and discussing our new EXOTHANE(TM) Elastomers product line . If you would like to schedule a meeting with use, please send an email to techsupport@esstechinc.com. Sign up for our Monthly [...]]]></description>
			<content:encoded><![CDATA[<p><img src="file:///C:/Users/TOM%7E1.ESS/AppData/Local/Temp/moz-screenshot.png" alt="" /></p>
<p>Esstech will be attending the <a href="http://www.uvebeast.com/" target="_blank">UV.EB East</a> Show in Syracuse, NY from October 4th to the 5th.</p>
<p>We look forward to seeing everyone, making appointments and discussing our new <a href="http://esstechinc.thomasnet.com/viewitems/all-categories/esstech-specialty-chemicals-exothane" target="_blank">EXOTHANE(TM) Elastomers </a>product line .</p>
<p>If you would like to schedule a meeting with use, please send an email to <a href="mailto:techsupport@esstechinc.com" target="_blank">techsupport@esstechinc.com</a>.</p>
<p><a href="http://www.uvebeast.com/" target="_blank"><img class="alignleft size-full wp-image-499" title="UV.EB East Logo" src="http://www.esstechinc.com/blog/wp-content/uploads/UV.EB-East-Logo1.jpg" alt="" width="413" height="137" /></a><br class="spacer_" /></p>
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 </strong></p>
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		<title>Optimal Diluent and Base Methacrylate Combinations</title>
		<link>http://esstechinc.com/blog/optimal-diluent-and-base-methacrylate-combinations/</link>
		<comments>http://esstechinc.com/blog/optimal-diluent-and-base-methacrylate-combinations/#comments</comments>
		<pubDate>Thu, 15 Sep 2011 12:38:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Research Paper]]></category>
		<category><![CDATA[Adhesive Monomer]]></category>
		<category><![CDATA[bis-GMA]]></category>
		<category><![CDATA[bisEMA]]></category>
		<category><![CDATA[DEGDMA]]></category>
		<category><![CDATA[diethyleneglycol]]></category>
		<category><![CDATA[diluent]]></category>
		<category><![CDATA[dimethacrylate]]></category>
		<category><![CDATA[EDMA]]></category>
		<category><![CDATA[EGDMA]]></category>
		<category><![CDATA[Shrinkage]]></category>
		<category><![CDATA[stress]]></category>
		<category><![CDATA[TETGDMA]]></category>
		<category><![CDATA[tetraethyleneglycol]]></category>
		<category><![CDATA[TMPTMA]]></category>
		<category><![CDATA[Triethyleneglycol]]></category>

		<guid isPermaLink="false">http://www.esstechinc.com/blog/?p=473</guid>
		<description><![CDATA[Influence of the base and diluent methacrylate monomers on the polymerization stress and its determinants N. R. G. Fróes-Salgado, L. C. Boaro, B. Pick, C. S. Pfeifer, C. E. Francci, M. M. Méier, R. R. Braga.  Journal of Applied Polymer Science. Overview: The correct pairing of methacrylate diluents and resins can optimize properties like polymerization [...]]]></description>
			<content:encoded><![CDATA[<div id="articleTitle">
<h1>Influence of the base and diluent methacrylate monomers on the polymerization stress and its determinants</h1>
</div>
<p id="doi">N. R. G. Fróes-Salgado, L. C. Boaro, B. Pick, C. S. Pfeifer, C. E. Francci, M. M. Méier, R. R. Braga.  Journal of Applied Polymer Science.</p>
<h3>Overview:</h3>
<p>The correct pairing of methacrylate diluents and resins can optimize properties like polymerization stress, volumetric shrinkage, degree of conversion, maximum rate of polymerization,  and elastic modulus in composite formulations.</p>
<h3>Abstract:</h3>
<div>
<p>The aim of this study was to  evaluate the effect of the association between <a href="http://esstechinc.thomasnet.com/item/resins/bisgma/x-950-0000?" target="_blank">bisphenol-A diglycidyl  dimethacrylate (BisGMA)</a> or its ethoxylated version <a href="http://esstechinc.thomasnet.com/item/resins/ethoxylated-bis-phenol-a-dimethacrylate/x-970-0000?" target="_blank">(BisEMA) </a>with  diluents derived from the <a href="http://esstechinc.thomasnet.com/viewitems/high-purity-monomers/ethyleneglycol-dimethacrylate?&amp;bc=100|1007" target="_blank">ethylene glycol dimethacrylate (EGDMA)</a>, with  increasing number of ethylene glycol units (1: <a href="http://esstechinc.thomasnet.com/viewitems/high-purity-monomers/ethyleneglycol-dimethacrylate?&amp;bc=100|1007" target="_blank">EGDMA</a>, 2: <a href="http://esstechinc.thomasnet.com/category/difunctional-monomers?" target="_blank">DEGDMA</a>, 3:  <a href="http://esstechinc.thomasnet.com/viewitems/difunctional-monomers/triethyleneglycol-dimethacrylate?" target="_blank">TEGDMA</a>, or 4: <a href="http://esstechinc.thomasnet.com/item/difunctional-monomers/tetraethyleneglycol-dimethacrylate/x-945-7446?" target="_blank">TETGDMA</a>), or <a href="http://esstechinc.thomasnet.com/viewitems/difunctional-monomers/trimethylolpropane-trimethacrylate?" target="_blank">trimethylol propane trimethacrylate (TMPTMA)</a> or <a href="http://esstechinc.thomasnet.com/viewitems/difunctional-monomers/1-12-dodecanediol-dimethacrylate?" target="_blank">1,10-decanediol dimethacrylate (D<sub>3</sub>MA)</a> on polymerization stress, volumetric shrinkage, degree of conversion, maximum rate of polymerization (<em>Rp</em><sub>max</sub>),  and elastic modulus of experimental composites. BisGMA containing  formulations presented lower shrinkage and stress but higher modulus and  <em>Rp</em><sub>max</sub> than those containing BisEMA. TMPTMA  presented the lowest stress among all diluents, as a result of lower  conversion. EGDMA, DEGDMA, TEGDMA, and TETGDMA presented similar  polymerization stress which was higher than the stress presented by D<sub>3</sub>MA and TMPTMA. D<sub>3</sub>MA  presented similar conversion when copolymerized with both base  monomers. The other diluents presented higher conversion when associated  with BisEMA. EGDMA showed similar shrinkage compared with DEGDMA and  higher than the other diluents. The lower conversion achieved by TMPTMA  did not jeopardize its elastic modulus, similar to the other diluents.  Despite the similar conversion presented by D<sub>3</sub>MA in  comparison with EGDMA and DEGDMA, its lower elastic modulus may limit  its use. Rather than proposing new materials, this study provides a  systematic evaluation of off the shelf monomers and their effects on  stress development, as highlighted by the analysis of conversion,  shrinkage and modulus, to aid the optimization of commercially available  materials. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011</p>
<p><br class="spacer_" /></p>
</div>
<p>LINK: <a href="http://onlinelibrary.wiley.com/doi/10.1002/app.34947/full" target="_blank"> http://onlinelibrary.wiley.com/doi/10.1002/app.34947/full</a></p>
<p>Article first published online: 1 SEP 2011.  DOI: 10.1002/app.34947</p>
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