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	<title> &#187; anthrax</title>
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		<title>Bacillus globigii spores in terbium reagent</title>
		<link>http://www.spectroscopytips.com/apps/bacillus-globigii-spores-in-terbium-reagent/</link>
		<comments>http://www.spectroscopytips.com/apps/bacillus-globigii-spores-in-terbium-reagent/#comments</comments>
		<pubDate>Tue, 09 Feb 2010 14:39:15 +0000</pubDate>
		<dc:creator>Admin</dc:creator>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[anthrax]]></category>
		<category><![CDATA[Fluorescence]]></category>
		<category><![CDATA[security]]></category>

		<guid isPermaLink="false">http://www.spectroscopytips.com/apps/?p=132</guid>
		<description><![CDATA[Goal: Illustrate the effect of the variable delay microcode on the shape of the terbium spectrum Hardware Used: USB2000-FLG EG&#38;G pulsed xenon light source CUV-ALL-UV 600 micron optical fibers Acquisition Parameters: Integration Time (msec): 10 Spectra Averaged: 100 Boxcar Smoothing: 20 Measurement Mode: Gated Fluorescence Experimental Conditions: The sample used was Bacillus globigii spores in [...]]]></description>
			<content:encoded><![CDATA[<p><strong>Goal:</strong><br />
Illustrate the effect of the variable delay microcode on the shape of the terbium spectrum<span id="more-132"></span></p>
<p><strong>Hardware Used:</strong><br />
USB2000-FLG<br />
EG&amp;G pulsed xenon light source<br />
CUV-ALL-UV<br />
600 micron optical fibers</p>
<p><strong>Acquisition Parameters:</strong><br />
Integration Time (msec): 10<br />
Spectra Averaged: 100<br />
Boxcar Smoothing: 20</p>
<p><strong>Measurement Mode:</strong><br />
Gated Fluorescence</p>
<p><strong>Experimental Conditions:</strong><br />
The sample used was Bacillus globigii spores in terbium reagent. Data acquisition delayed from 5 to 500 usec after the lamp was triggered.</p>
<p><strong>Results:</strong><br />
The effect of gating on the spectral shape is shown in the figures below. As the delay between lamp trigger and data acquisition is increased, the terbium/DPA photoluminescence becomes more distinct. Shorter lived background fluorescence and lamp pulse are not observed. Longer delay times (above 50 usec) lead to a decrease in sensitivity as a portion of the terbium/DPA photoluminescence is missed at long delay times.</p>
<p><strong>Conclusions:</strong><br />
The optimal delay for these samples is 40 microseconds. A 40 microsecond delay between the lamp trigger and data acquisition minimizes the contribution of the xenon source (and fluorescence due to other fluorophores) to the photoluminescence spectrum while maximizing the photoluminescence signal.</p>
<p><strong>Images:</strong></p>
<p><img class="aligncenter size-full wp-image-133" title="ip1" src="http://www.spectroscopytips.com/apps/wp-content/uploads/ip1.jpg" alt="" width="500" height="263" /></p>
<p><img class="aligncenter size-full wp-image-134" title="ip2" src="http://www.spectroscopytips.com/apps/wp-content/uploads/ip2.jpg" alt="" width="500" height="263" /></p>
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