Thank You

TLC Orchids and Such <[EMAIL PROTECTED]> wrote:IV Iodine Value


----- Original Message ----- 
From: "Keith Addison" 
To: 
Sent: Saturday, April 02, 2005 7:50 AM
Subject: [Biofuel] Re: soybeanoil a bad choice for BD making?


> >Hi you fine people
> >I read a lot about IV and have not been able to figure out what it is.
> >I'm new to all this.
> >Would someone PLEASE help me out here?
> >Thanks
> >Roy
>
> Hello Roy
>
> I gave you this before:
>
> Start here:
> "Where do I start?"
> http://journeytoforever.org/biodiesel_make.html#start
>
> That's on this page:
> http://journeytoforever.org/biodiesel_make.html
> Make your own biodiesel: Journey to Forever
>
> Read the whole thing, and then keep going.
>
> You'll find this on that page:
>
> Iodine Values
> -- High Iodine Values
> -- Talking about the weather
>
> All you need to know about IV.
>
> Best wshes
>
> Keith
>
>
> >TLC Orchids and Such wrote:
> >
> >
> >Hydrogenated canola has an IV of around 65 while non hydrogenated has an
IV
> >of around 112.
> >Does anyone know if the IV in soybean (131) safflower (145) hemp (165) or
> >sunflower (133)
> >are altered in any way by the hydrogenation process?
> >
> >----- Original Message -----
> >From: "bob allen"
> >To:
> >Sent: Friday, April 01, 2005 3:24 PM
> >Subject: Re: [Biofuel] Re: soybeanoil a bad choice for BD making?
> >
> >
> > >
> > > Howdy Kieth and Jan
> > >
> > >
> > > At the risk of looking foolish as I am an organic chemist, but don't
> > > have much experience with polymer chemistry- here goes
> > >
> > >
> > > Polymerization is a molecule molecule reaction. A compound with double
> > > carbon carbon bond is particularly susceptible free radical oxidation.
> > > Let's call them U. Compounds without carbon carbon double bounds are
> > > relatively unreactive. We will call these S. Oxygen will activate one
> > > molecule, U, but for polymerization to occur, the activated molecule
> > > must encounter another U, then the now covalently bonded pair, must
> > > encounter another U, and so on. Collisions of activated U with S don't
> > > result in a reaction.
> > >
> > >
> > > It seems to me that if you "dilute" U with S, that you will reduce
> > > polymerization.
> > >
> > > Or how about this. An activated molecule has only a finite amount of
> > > time to react. If an activated molecule U "bumps into" another U then
> > > chain growth continues. But if activated U bumps into S, no reaction
> > > occurs, other than U reacting internally, which also stops chain
growth.
> > >
> > >
> > > Polymer chemists can modulate the number of molecules in a chain
(chain
> > > length) by addition of non polymerizing stuff.
> > >
> > >
> > > Being a right brain guy, this discussion is made more difficult, as I
> > > can't draw all the pictures which exemplify the points I am trying to
> > > make. :(
> > >
> > >
> > > The long and short of it (no pun intended) chain length of polymers
> > > will be reduced by dilution of biodiesel blended from high IV oils
with
> > > low IV oils. Put another way, the time to reach a specified degree of
> > > polymerization will be extended by dilution.
>
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>
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Roy Washbish 
Certified Health Coach 
A HOME BUSINESS & PRODUCTS THAT WORK
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