<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://wiki.blig-blug.com/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Chem+Nov</id>
	<title>DMT-Nexus Wiki - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="https://wiki.blig-blug.com/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Chem+Nov"/>
	<link rel="alternate" type="text/html" href="https://wiki.blig-blug.com/Special:Contributions/Chem_Nov"/>
	<updated>2026-11-14T09:43:28Z</updated>
	<subtitle>User contributions</subtitle>
	<generator>MediaWiki 1.43.11</generator>
	<entry>
		<id>https://wiki.blig-blug.com/w/index.php?title=Talk:Noman%27s_tek&amp;diff=14554</id>
		<title>Talk:Noman&#039;s tek</title>
		<link rel="alternate" type="text/html" href="https://wiki.blig-blug.com/w/index.php?title=Talk:Noman%27s_tek&amp;diff=14554"/>
		<updated>2020-02-16T14:52:43Z</updated>

		<summary type="html">&lt;p&gt;Chem Nov: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;So for Normans tek it is encouraged to scrub the jars and utensils used in the extraction with cannabis/salvia?&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
I&#039;ve done a few things differently, and I think the results are good.  First, I do only 50 grams at a time, because it becomes time-consuming to separate large amounts.  Too much plant fiber also makes it difficult to separate.  It&#039;s very important to pour a trickle at a time in a separatory funnel (I highly recommend investing in one) to avoid getting plant fiber in, which gums up the works.  &lt;br /&gt;
&lt;br /&gt;
You preferably want to get the oily NAPTHA layer out without much aqueous layer.  Just do a single pour with each separation.  Don&#039;t worry about getting every single drop out because you will just make a headache for yourself.  A wire mesh might be a good idea here, but I don&#039;t use one.  A filter simply becomes too clogged.&lt;br /&gt;
&lt;br /&gt;
I typically start by mixing my distilled water and lye with the finely ground bark, add my NAPTHA.  I do a couple minutes of mixing and then just set it aside for when I have time.  Rather than letting it soak on the last step, I leave it a day or even a week like this and occasional turn it if I have time.  I do four naptha separations with ~50ml each time at this point.  Once I&#039;ve finished this, I go right to the wash.  Freezing the product and redissolving before the wash seems to be a redundant and pointless time waster.  I use 50ml distilled water with a pinch of Na Carbonate.  DON&#039;T overdo this.  I messed up my very first batch by doing too much.  Simply turn the funnel 5 times or so and then quickly separate.  Then 8 hours of freezing does the job. &lt;br /&gt;
&lt;br /&gt;
I don&#039;t scrub with herbs, as I don&#039;t use them, so after filtering my product out I simply pour the NAPTHA back into the jar and allow the product to redissolve for my next extraction.  This way I&#039;m getting as much as possible through 4-50g extractions.  Yields are good and getting better with these tweaks.  I didn&#039;t get a good measurement last time, but this one is better and I will report the next two.  The basic process Noman gives is a good one.  I recommend against the article in the wiki calling for 4 washes with one having Na Carbonate and three being distilled water.  This is a great way to lose your product if done incorrectly.  The product I&#039;ve had is 100% tolerable and produces the desired results in experiments performed.  I&#039;ve yet to try recrystallization, as I&#039;m afraid to screw it up, but the next round of experiments might be the time I try.  Chemistry is fun!&lt;/div&gt;</summary>
		<author><name>Chem Nov</name></author>
	</entry>
</feed>