Hi Tom

Many thanks for the advice. I will let you know how I get on.
I intend (hopefully) to run B100 in my boiler. I was planning to ask  
about the adjustments I will have to make! I have set up a T-piece on  
the fuel feed so I can try small amount of different % to see how I go.

Best

Charles

On 21/06/2006, at 2:30 AM, Thomas Kelly wrote:

> Charles,
>      Then creamy canola it is.
>
>      It sounds as though you are getting a reaction  .....
> methanol test tells us it is not complete.
>
>      Could be the KOH
>
>      I have gotten new caustic that was not the concentration the  
> seller (or
> the bag) said it was.
>
>      Do you have (or can you get) a sample of KOH (or NaOH) of  
> known purity?
>      You could titrate a sample of the WVO with the caustic of  
> known purity
> and then titrate the same oil w. the new, questionable KOH. A  
> comparison of
> the titrations on the same WVO would indicate its purity.
>      I would do it like this: (corrections appreciated)
> 1. Divide the titration for the known by the titration for the
>     unknown.  (Titration is inverse to concentration)
> 2. Multiply result by the conc. of the known.
>
> Ex: Known KOH is 85% and titration = 3.0 g/L
>       "Unknown" KOH titrates  3.6 g/L
>
> 1.     3.0 divided by  3.6  =  0.83333
> 2.     0.83333  X  .85   =   .708
>         "Unknown" =  70.8%  KOH
>
> **** If the Known caustic is NaOH, then multiply its titration by  
> 1.4  prior
> to step 1.
>
> You wrote:
> "Bottom layer (20%) is solid and dark redy- brown (glycerine I  
> hope) then
> thin layer (5%) what looks like
> unreacted oil, then rest is dark brown "bio".  It passes the wash  
> test and
> the third wash leaves clean water underneath and brown "bio" on  
> top. The
> "bio" also leaves about 20-30% residue in the methanol test."
>
> Bottom layer:  glycerine, I think
> Top layer:   biodiesel + unreacted glycerides (that
>                   precipitate out in the methanol test)
> Middle layer: soaps?    3.6g KOH/L WVO titration
>                   suggests you will get some soap, but I think
>                   5% is a bit high ... especially if you are not
>                   using enough caustic.
>    Could there be water in the oil (does it sizzle/pop when heated?)
>     Be patient.
>     Check the KOH.
>     Heat a sample of the oil. Stir it ... be careful, if there's  
> water in it
> will spatter.
>                      Hang in there,
>                                    Tom
> P.S.
>      What % biodiesel do you intend to burn in your boiler?
>      Any adjustments to the burner (pressure, nozzle, air flow?)
>      (Just curious)
>
> ----- Original Message -----
> From: "Charles List" <[EMAIL PROTECTED]>
> To: <biofuel@sustainablelists.org>
> Sent: Monday, June 19, 2006 6:38 PM
> Subject: Re: [Biofuel] Help needed!
>
>
>> Hi Tom
>>
>> Right, feel I'm making some progress. After a very cold night (-6C) I
>> can now see three layers in my 1l test batch of creamy canola if I
>> shine a light behind it. Bottom layer (20%) is solid and dark redy-
>> brown (glycerine I hope) then thin layer (5%) what looks like
>> unreacted oil, then rest is dark brown "bio".  It passes the wash
>> test and the third wash leaves clean water underneath and brown "bio"
>> on top. The "bio" also leaves about 20-30% residue in the methanol  
>> test.
>>
>> So, from this, if I assume my KOH is at fault (Occum's razor) then is
>> there an easy way I can tell how much more KOH to add to compensate?
>>
>> In answer to your questions, the pre-treated oil turns very dark
>> brown, almost black on heating past 25 degrees C and it titrates at
>> 3.6ml (I use KOH for the titration too).
>>
>> My supply of normal canola has dried up as the restaurant owner has
>> sold up and it is changing into an Indian take-away- so creamy canola
>> is all I have to work with!!
>>
>> Best
>>
>> Charles
>>
>>
>>
>> On 20/06/2006, at 4:25 AM, Thomas Kelly wrote:
>>
>>> Charles,
>>>      I think you would get a split, whether your chemicals were
>>> pure or
>>> somewhat contaminated. The problem would be more a matter of
>>> achieving a
>>> complete reaction.
>>> i.e. You would get biodiesel, but it might not pass quality tests.
>>>
>>>       I admit to being as perplexed as you
>>>
>>>           Is it correct to say that your first problems arose  
>>> when you
>>> started using the "creamy canola oil"?
>>>    (150 L batch and now w. 70L and even 1L batches).
>>>
>>>      When I hear creamy oil I think animal fat and/or water buzzed
>>> into the
>>> oil by the impelled in a pump.
>>>
>>>      Do you pre-heat it before processing? If so, does it turn
>>> clear? You
>>> mention that the oil turns solid at 10C (50F). This suggests that
>>> the oil
>>> contains some animal fat ..... from cooking. The canola oil I've  
>>> used
>>> remained liquid below 10C.
>>>      How does the color of the oil, after heating, compare to the
>>> color of
>>> the "biodiesel" you made?  I've made some very dark BD from very
>>> dark WVO.
>>> (see archives: "Very Dark Biodiesel, help needed"  Oct 20/05) I
>>> couldn't see
>>> the split w/o very bright light.
>>>
>>>       Let's just consider one or two things:
>>> 1.  You have done several successful test batches using virgin oil
>>> and then
>>> WVO so that you are on solid ground as to the measurements and
>>> procedure. In
>>> fact you have been successful scaling up to 40L. (I assume you  
>>> used a
>>> different WVO)
>>>
>>>  2. Re: your recent 1 L test batch:
>>>    You cannot see any split even when viewed w. a bright
>>>     light?
>>>     Remove a sample from the top and a sample from the bottom.
>>> (Keep them
>>> separate.)
>>>     Perform a wash test on each sample. Do the samples behave
>>> differently
>>> (from each other) when you perform a "wash test" on them?
>>>
>>>      What did you get for a titration on the oil?
>>>
>>>      If all else fails, you may have to go to other sources of WVO.
>>> You had
>>> success up to 40L. You got clear cut splits, BD that washed, and
>>> may well
>>> have passed quality tests. Before frustration overwhelms you it
>>> might be a
>>> good idea to go back to where you were successful. Scale up using
>>> the same
>>> WVO that you were successful with and perform quality test to fine
>>> tune your
>>> process. If this "creamy canola" still fascinates you, do some 1L.
>>> test
>>> batches with it.
>>>      You mentioned New Zealand; winter on your doorstep. Gotta  
>>> get you
>>> making heating fuel. I'm on the other side of the equator ....
>>> summer's
>>> heating up.
>>>      Good luck, and let me know how it goes.
>>>                                                      Tom
>>>
>>>
>>>
>>> ----- Original Message -----
>>> From: "Charles List" <[EMAIL PROTECTED]>
>>> To: <biofuel@sustainablelists.org>
>>> Sent: Sunday, June 18, 2006 4:29 PM
>>> Subject: Re: [Biofuel] Help needed!
>>>
>>>
>>>> Hi Tom
>>>>
>>>> Thanks for that, I tried 70l at the weekend and end-product still
>>>> black, so I tried a 1l batch, still black!! I am using new KOH and
>>>> new methanol (as I'm scaling up I bought in bulk for the first  
>>>> time)
>>>> so could it be one of these that's the problem? If so, how do I  
>>>> test
>>>> if they're any good? I'm getting some kind of reaction as the black
>>>> product is liquid at zero Celsius, and my oil is solid at 10  
>>>> degrees,
>>>> but I can't see any split at all and, as I said, the product is  
>>>> very
>>>> very dark brown, almost black!!
>>>>
>>>> Charles
>>>>
>>>>
>>>> On 17/06/2006, at 1:59 AM, Thomas Kelly wrote:
>>>>
>>>>> Charles,
>>>>>      I think that if you drop back to 80 L you are still making a
>>>>> goodly bit
>>>>> of fuel. You still may have to tweak the process  ... increase  
>>>>> time
>>>>> and or
>>>>> temp. Get it right there and then go up in 5 or 10L increments,
>>>>> testing each
>>>>> batch, and again, tweaking, if necessary.
>>>>>      I went from small test batches and slowly increased volume up
>>>>> to 20 -
>>>>> 25 L batches. I then jumped up to 130L batches.
>>>>>     When I discovered that the biodiesel wasn't as good as I
>>>>> thought, I
>>>>> dropped back to 76L (20 gal)batches. After increasing processing
>>>>> time and
>>>>> then increasing temp to 140F (60C) , I finally began to
>>>>> consistently make BD
>>>>> that passed the "methanol solubility test" and did not drop out
>>>>> additional
>>>>> glycerine when I reprocessed 1L of finished product.
>>>>>      The limitation on my system seems to be about 91L (24 gal)
>>>>> and is
>>>>> probably the volume limit of my pump, a 1" Clearwater pump.
>>>>>      I still quality test each batch, not just to be sure of the
>>>>> fuel, but
>>>>> as a maintenance test for the processor and the materials being
>>>>> used. Is my
>>>>> recovered methanol pure enough? (If I use the first 4 gal I
>>>>> recover, the BD
>>>>> passes the quality test. When I use the first 6 gallons, little
>>>>> buggers show
>>>>> up in the methanol sol. test).
>>>>>      Slow and methodical pays off.
>>>>>      Best of luck.
>>>>>      Let me know how it goes,
>>>>>                                                 Tom
>>>
>>>
>>>
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>>
>>
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