Re: CSliposomes ultrasonic cleaners

2010-06-24 Thread Ode Coyote



 50/60 Hz is nowhere near ultrasonic.
Methinks you be reading the power input label, not what it outputs.

Ultrasound is cyclic http://en.wikipedia.org/wiki/Soundsound pressure 
with a http://en.wikipedia.org/wiki/Frequencyfrequency greater than the 
upper limit of http://en.wikipedia.org/wiki/Humanhuman 
http://en.wikipedia.org/wiki/Hearing_%28sense%29hearing. Although this 
limit varies from person to person, it is approximately 20 
http://en.wikipedia.org/wiki/Hertzkilohertz (20,000 hertz) in healthy, 
young adults and thus, 20 kHz serves as a useful **lower** limit in 
describing ultrasound.


You can hear 60 Hz   60 cycle hum the bane of music lovers the world 
round...unless it's 50 cycle hum.


Like with push/pull audio amplifiers, I imagine that the sound wave 
pressures are both positive and negative  alternating pressure/vacuum 
cycles.

Ultrasonic Cleaner ...at the doggie brain wash frequented by jewelry.
Essentially a good audio amp cranked to the max, a piezoelectric tweeter 
and mind bendingly screaming loud bat music, all played in a bowl of water.


Ode


At 09:01 AM 6/23/2010 -0500, you wrote:
I have been doing some study on the mechanics of ultrasonic cleaners in 
relation to liposomes and I am curious of some of the ramifications:


1)  Ultrasonic cleaners work by producing alternating low and high sound 
waves. The unit I am using does 50/60 Hz. The low phase produces the 
bubble and the high phase implodes the bubbles which produces the cleaning 
action so desired in such cleaners. Question: I can see the low phase 
producing liposomes, but how are the liposomes immune to the high phase 
that normally ruptures bubbles?


doug



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Re: CSliposomes ultrasonic cleaners

2010-06-24 Thread Dorothy Fitzpatrick
Brooks said that liposomals made with blenders are only about 25% absorbable, 
compared to 75% in the cleaners.  dee

On 23 Jun 2010, at 20:58, Nenah Sylver wrote:

 I have a vitamix blender and wonder how effective such a blender would be on 
 producing liposomes? Note that the vitamix is no ordinary blender! Blades 
 reach 264 mph one way and they can be instantaeously reversed at the same 
 speed to produce a blade affect collisions in excess of 500 mph. . . . It 
 seems to me that the vitamix performance might approach the advertised 
 pressures/forces of Livon Lab's 1700 psi liposomal making procedure though I 
 don't know how to equate mph vs psi? Granted, the vitamix because it can 
 produce high temps, one would need to use care to make lip-C via pulsing and 
 other ways, but that is easy to get around, I should think.
 =
 Doug,
 Someone wrote me privately and said he got good results with his VitaMix. 
 People who took his Lip. C. made in the VitaMix got better.
  
 Nenah
  


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Re: CSliposomes ultrasonic cleaners

2010-06-24 Thread Dorothy Fitzpatrick
I do love this list for the oh-so-clever people we have on it!  Fascinating 
stuff.  dee

On 23 Jun 2010, at 21:08, Norton, Steve wrote:

 Doug,
 I am not an expert but here is my opinion on your questions.
 
 1) I think that your ultrasonic transducer operates at a frequency around 42 
 kHz and not 50/60 Hz. The bubbles that rupture are bubbles of gas. The 
 liposome bubbles that form consist of a phospholipid shell with a water 
 center. Since the liposome bubble is not gaseous it does not rupture in the 
 same way that gas bubbles do. That does not mean that shear forces do not 
 rupture some lipisomes but I expect that the liposomes reform after the shear 
 forces go away.
 
 2) The ultrasonic waves apply shear forces to break the lecithin into 
 individual phospholipids that will then form liposomes See:
 http://en.wikipedia.org/wiki/Liposome
 It should be noted that formation of liposomes and nanoliposomes is not a 
 spontaneous process. Lipid vesicles are formed when phospholipids such as 
 lecithin are placed in water and consequently form one bilayer or a series of 
 bilayers, each separated by water molecules, once enough energy is supplied 
 [8]. Liposomes can be created by sonicating phospholipids in water[3]. Low 
 shear rates create multilamellar liposomes, which have many layers like an 
 onion. Continued high-shear sonication tends to form smaller unilamellar 
 liposomes. In this technique, the liposome contents are the same as the 
 contents of the aqueous phase.
 


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CSliposomes ultrasonic cleaners

2010-06-23 Thread polo
I have been doing some study on the mechanics of ultrasonic cleaners in 
relation to liposomes and I am curious of some of the ramifications: 

1)  Ultrasonic cleaners work by producing alternating low and high sound waves. 
The unit I am using does 50/60 Hz. The low phase produces the bubble and the 
high phase implodes the bubbles which produces the cleaning action so desired 
in such cleaners. Question: I can see the low phase producing liposomes, but 
how are the liposomes immune to the high phase that normally ruptures bubbles?

2)  Using the cheap harbor freight ultrasonic cleaner, it is recommended to 
stir the solution and that the more shallow the solution, the higher the 
quality of liposome. Is stirring really necessary as it is so time consuming? 
It seems to me that the solution has natural movement all by itself from the 
production of the ultrasonic waves. 

3)  It is suggested that the best cavitation of the solution in the ultrasonic 
cleaner occurs when the solution is warm, plus the cavittion produces heat too. 
How much danger is this produced heat from ultrasonic wave production to 
ascorbic acid or the ascorbates' integrity over a long period of time? Is it 
minimal? One would logically conclude that the more heat produced, the more 
energetic the cavitation---would one not? If this is true, would it not be more 
efficient to produce liposomes with specialized instruments like sonifiers 
(pulsing and placing the lipo-C in ice water to keep temps low)? 

4)  It sounds to me that the longer one can run your lipo-C solution in a 
ultrasonic cleaner the better the quality of liposomes according to some of 
Brooks' later posts, however there is what is known as degassing in 
ultrasonic cleaning. Many instruction manuals for cleaners will advise you to 
de-gas your solution from 5-10 minutes before actually starting the cleaning 
process. Degassing is the initial removal of gases present in the solution. 
Useful cavitation occurs after the gasses have been removed from the solution 
leaving a vacuum in the later formed bubbles as it is written in these manuals. 
So it seems to me on first glance after reading this, that one would not want 
to extend our Lipo-C solution cavitation much longer than the recommended 6 
minutes as that would degas the solution, producing an empty bubble. Is this 
true or am I missing some thing? 

5)  Finally, there seems to me, better ways to produce a liposome via sound 
waves. Would not lab devices known as sonifiers/sonicators/cell disruptors be a 
better choice since these devices produce an intense steady frequency unlike 
the ultrasonic cleaner? Agreed, this device would not be in the reach of the 
average home-made tech, but would it produce a smaller, better liposome than 
ultrasonic cleaners? I realize that heat generation would be a problem from 
such intense ultrasound involvement from a cell disruptor, but having the 
solution in ice and pulsing should over come this problem, eh?

doug

Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread Dorothy Fitzpatrick
I too would like the answers to these questions Doug.  I don't think the heat 
thing would be a problem because the heating is minimal, I believe it is only 
high heat which destroys Vit C, but it would be nice to *know*.  dee

On 23 Jun 2010, at 15:01, polo wrote:

 I have been doing some study on the mechanics of ultrasonic cleaners in 
 relation to liposomes and I am curious of some of the ramifications:
  
 1)  Ultrasonic cleaners work by producing alternating low and high sound 
 waves. The unit I am using does 50/60 Hz. The low phase produces the bubble 
 and the high phase implodes the bubbles which produces the cleaning action so 
 desired in such cleaners. Question: I can see the low phase producing 
 liposomes, but how are the liposomes immune to the high phase that normally 
 ruptures bubbles?
  
 2)  Using the cheap harbor freight ultrasonic cleaner, it is recommended to 
 stir the solution and that the more shallow the solution, the higher the 
 quality of liposome. Is stirring really necessary as it is so time consuming? 
 It seems to me that the solution has natural movement all by itself from the 
 production of the ultrasonic waves.
  
 3)  It is suggested that the best cavitation of the solution in the 
 ultrasonic cleaner occurs when the solution is warm, plus the cavittion 
 produces heat too. How much danger is this produced heat from ultrasonic wave 
 production to ascorbic acid or the ascorbates' integrity over a long period 
 of time? Is it minimal? One would logically conclude that the more heat 
 produced, the more energetic the cavitation---would one not? If this is true, 
 would it not be more efficient to produce liposomes with specialized 
 instruments like sonifiers (pulsing and placing the lipo-C in ice water to 
 keep temps low)?
  


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Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread Marshall Dudley

polo wrote:
I have been doing some study on the mechanics of ultrasonic cleaners 
in relation to liposomes and I am curious of some of the ramifications:
 
1)  Ultrasonic cleaners work by producing alternating low and high 
sound waves. The unit I am using does 50/60 Hz. The low phase produces 
the bubble and the high phase implodes the bubbles which produces the 
cleaning action so desired in such cleaners. Question: I can see the 
low phase producing liposomes, but how are the liposomes immune to the 
high phase that normally ruptures bubbles?
 
50/60 Hz is the line frequency the unit is specified to work with, what 
comes in the power cord.  That is on the low end of the audio spectrum, 
not the high.  Cleaners typically run between 20 and 30 KHz, which is 
above the range of hearing. The movement is basically sinusoidal, thus 
the amount of time above the baseline is equal to the amount under the 
baseline.  The word phase in such a situation would refer to the 
difference in the angle between two waves and does not apply to these 
cleaners at all.


Marshall


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Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread polo
Oh, I forgot to include one other musing on this subject. I have a vitamix 
blender and wonder how effective such a blender would be on producing 
liposomes? Note that the vitamix is no ordinary blender! Blades reach 264 mph 
one way and they can be instantaeously reversed at the same speed to produce a 
blade affect collisions in excess of 500 mph. Also, the vitamix can generate so 
much turbulance, it can reach cooking temperatures in minutes. This is 
certainly no ordinary run of the mill kitchen blender. 

It seems to me that the vitamix performance might approach the advertised 
pressures/forces of Livon Lab's 1700 psi liposomal making procedure though I 
don't know how to equate mph vs psi? Granted, the vitamix because it can 
produce high temps, one would need to use care to make lip-C via pulsing and 
other ways, but that is easy to get around, I should think. 

doug

Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread polo
Ok, thanks for that info, but nevertheless, this tidbit does not change the 
fact that ultrasonic cleaners are designed to have a low and high phase. How 
can a liposome be immune from rupture, by the tough phospholipids membrane 
when compared to the ordinary bubble??


doug


- Original Message - 

50/60 Hz is the line frequency the unit is specified to work with, what
comes in the power cord.  That is on the low end of the audio spectrum,
not the high.  Cleaners typically run between 20 and 30 KHz, which is
above the range of hearing. The movement is basically sinusoidal, thus
the amount of time above the baseline is equal to the amount under the
baseline.  The word phase in such a situation would refer to the
difference in the angle between two waves and does not apply to these
cleaners at all.



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Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread Dan Nave
By virtue of their relative sizes?

Dan


On Wed, Jun 23, 2010 at 2:40 PM, polo dah...@centurytel.net wrote:
 Ok, thanks for that info, but nevertheless, this tidbit does not change the
 fact that ultrasonic cleaners are designed to have a low and high phase. How
 can a liposome be immune from rupture, by the tough phospholipids membrane
 when compared to the ordinary bubble??

 doug


 - Original Message -

 50/60 Hz is the line frequency the unit is specified to work with, what
 comes in the power cord.  That is on the low end of the audio spectrum,
 not the high.  Cleaners typically run between 20 and 30 KHz, which is
 above the range of hearing. The movement is basically sinusoidal, thus
 the amount of time above the baseline is equal to the amount under the
 baseline.  The word phase in such a situation would refer to the
 difference in the angle between two waves and does not apply to these
 cleaners at all.


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RE: CSliposomes ultrasonic cleaners

2010-06-23 Thread Nenah Sylver
I have a vitamix blender and wonder how effective such a blender would be on
producing liposomes? Note that the vitamix is no ordinary blender! Blades
reach 264 mph one way and they can be instantaeously reversed at the same
speed to produce a blade affect collisions in excess of 500 mph. . . . It
seems to me that the vitamix performance might approach the advertised
pressures/forces of Livon Lab's 1700 psi liposomal making procedure though I
don't know how to equate mph vs psi? Granted, the vitamix because it can
produce high temps, one would need to use care to make lip-C via pulsing and
other ways, but that is easy to get around, I should think.

=

Doug,

Someone wrote me privately and said he got good results with his VitaMix.
People who took his Lip. C. made in the VitaMix got better.

 

Nenah

 

Nenah Sylver, PhD

electromedicine specialist and author

The Rife Handbook of Frequency Therapy (2009)

 The Holistic Handbook of Sauna Therapy (2004)

 http://www.nenahsylver.com www.nenahsylver.com 

  _  

From: polo [mailto:dah...@centurytel.net] 
Sent: Wednesday, June 23, 2010 12:37 PM
To: silver-list@eskimo.com
Subject: Re: CSliposomes  ultrasonic cleaners

 

Oh, I forgot to include one other musing on this subject. 

 

doug



RE: CSliposomes ultrasonic cleaners

2010-06-23 Thread Norton, Steve
Doug,
I am not an expert but here is my opinion on your questions.

1) I think that your ultrasonic transducer operates at a frequency around 42 
kHz and not 50/60 Hz. The bubbles that rupture are bubbles of gas. The liposome 
bubbles that form consist of a phospholipid shell with a water center. Since 
the liposome bubble is not gaseous it does not rupture in the same way that gas 
bubbles do. That does not mean that shear forces do not rupture some lipisomes 
but I expect that the liposomes reform after the shear forces go away.

2) The ultrasonic waves apply shear forces to break the lecithin into 
individual phospholipids that will then form liposomes See:
http://en.wikipedia.org/wiki/Liposome
It should be noted that formation of liposomes and nanoliposomes is not a 
spontaneous process. Lipid vesicles are formed when phospholipids such as 
lecithin are placed in water and consequently form one bilayer or a series of 
bilayers, each separated by water molecules, once enough energy is supplied 
[8]. Liposomes can be created by sonicating phospholipids in water[3]. Low 
shear rates create multilamellar liposomes, which have many layers like an 
onion. Continued high-shear sonication tends to form smaller unilamellar 
liposomes. In this technique, the liposome contents are the same as the 
contents of the aqueous phase.

As the article states, low shear rates create multilamellar liposomes, which 
have many layers like an onion. The goal is to generate high shear rates to 
create small liposomes. This can be done in small ultrasonic cleaners as well 
as in large ultrasonic cleaners. The shear rate is proportional to the energy 
in the solution and is usually defined by the watts/volume the transducer 
produces. You can adjust the watts/volume by simply by changing the amount of 
solution you put in the ultrasonic cleaner. The reason for the stirring is that 
standing waves generally form in the solution. This is evidenced by ripples on 
the top of the solution. If the ripples are stationary. Then the desired shear 
forces are not moving through the solution but are stationary. To evenly apply 
the shear forces to all the lecithin, you must then move the lecithin around by 
stirring.

3) The ultrasonic cleaner is a form of sonication. See: 
http://en.wikipedia.org/wiki/Sonication
 Sonication is the act of applying sound (usually ultrasound) energy to 
agitate particles in a sample, for various purposes. In the laboratory, it is 
usually applied using an ultrasonic bath or an ultrasonic probe, colloquially 
known as a sonicator.

4) Yes, gas in the solution reduces the effectiveness of the process because 
the gas bubbles absorb some of the ultrasonic energy. I don't know how long it 
takes to degas a solution but using distilled water for the solution will 
reduce the amount of dissolved gasses in the solution you start with.

 - Steve N

From: polo [mailto:dah...@centurytel.net] 
Sent: Wednesday, June 23, 2010 7:02 AM
To: silver-list@eskimo.com
Subject: CSliposomes  ultrasonic cleaners

I have been doing some study on the mechanics of ultrasonic cleaners in 
relation to liposomes and I am curious of some of the ramifications: 
 
1)  Ultrasonic cleaners work by producing alternating low and high sound waves. 
The unit I am using does 50/60 Hz. The low phase produces the bubble and the 
high phase implodes the bubbles which produces the cleaning action so desired 
in such cleaners. Question: I can see the low phase producing liposomes, but 
how are the liposomes immune to the high phase that normally ruptures bubbles?
 
2)  Using the cheap harbor freight ultrasonic cleaner, it is recommended to 
stir the solution and that the more shallow the solution, the higher the 
quality of liposome. Is stirring really necessary as it is so time consuming? 
It seems to me that the solution has natural movement all by itself from the 
production of the ultrasonic waves. 
 
3)  It is suggested that the best cavitation of the solution in the ultrasonic 
cleaner occurs when the solution is warm, plus the cavittion produces heat too. 
How much danger is this produced heat from ultrasonic wave production to 
ascorbic acid or the ascorbates' integrity over a long period of time? Is it 
minimal? One would logically conclude that the more heat produced, the more 
energetic the cavitation---would one not? If this is true, would it not be more 
efficient to produce liposomes with specialized instruments like sonifiers 
(pulsing and placing the lipo-C in ice water to keep temps low)? 
 
4)  It sounds to me that the longer one can run your lipo-C solution in a 
ultrasonic cleaner the better the quality of liposomes according to some of 
Brooks' later posts, however there is what is known as degassing in 
ultrasonic cleaning. Many instruction manuals for cleaners will advise you to 
de-gas your solution from 5-10 minutes before actually starting the cleaning 
process. Degassing is the initial removal of gases present

Re: CSliposomes ultrasonic cleaners

2010-06-23 Thread M. G. Devour
I think some clarification might help, polo.

Are you saying the US cleaner cycles between low amplitude and high 
amplitude, or switches between two different oscillator frequencies? 
The switching, whatever it is, you imply takes place at the 60 hz line 
frequency, which would certainly simplify circuit design.

Your use of the word 'phase' was just to refer to the two states the 
drivers switch between, right?

Sometimes you have to read a little deeper between the lines, Marshall. 
grin

Mike D.

 Ok, thanks for that info, but nevertheless, this tidbit does not change
 the fact that ultrasonic cleaners are designed to have a low and high
 phase. How can a liposome be immune from rupture, by the tough
 phospholipids membrane when compared to the ordinary bubble??
 
 doug
 
 
 - Original Message - 
  50/60 Hz is the line frequency the unit is specified to work with,
  what comes in the power cord.  That is on the low end of the audio
  spectrum, not the high.  Cleaners typically run between 20 and 30 KHz,
  which is above the range of hearing. The movement is basically
  sinusoidal, thus the amount of time above the baseline is equal to the
  amount under the baseline.  The word phase in such a situation would
  refer to the difference in the angle between two waves and does not
  apply to these cleaners at all.
 
 
 --
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[mdev...@eskimo.com]
[Speaking only for myself...   ]



RE: CSliposomes ultrasonic cleaners

2010-06-23 Thread Norton, Steve
I believe that Doug is referring to the rarefaction and compression phases of 
the ultrasonic wave in the cleaning solution.

 - Steve N


http://www.blackstone-ney.com/pdfs/T_Fundamentals.pdf
In elastic media such as air and most solids, there is a continuous
transition as a sound wave is transmitted. In non-elastic media such
as water and most liquids, there is continuous transition as long as
the amplitude or loudness of the sound is relatively low. As
amplitude is increased, however, the magnitude of the negative
pressure in the areas of rarefaction eventually becomes sufficient to
cause the liquid to fracture because of the negative pressure, causing
a phenomenon known as cavitation. Cavitation bubbles are created
at sites of rarefaction as the liquid fractures or tears because of the
negative pressure of the sound wave in the liquid. As the wave fronts
pass, the cavitation bubbles oscillate under the influence of positive
pressure, eventually growing to an unstable size. Finally, the violent
collapse of the cavitation bubbles results in implosions, which cause
shock waves to be radiated from the sites of the collapse. The collapse
and implosion of myriad cavitation bubbles throughout an
ultrasonically activated liquid result in the effect commonly associated
with ultrasonics. It has been calculated that temperatures in excess of 
10,000°F and pressures in
excess of 10,000 PSI are generated at the implosion sites of cavitation 
bubbles.



-Original Message-
From: M. G. Devour [mailto:mdev...@eskimo.com] 
Sent: Wednesday, June 23, 2010 11:13 AM
To: silver-list@eskimo.com
Subject: Re: CSliposomes  ultrasonic cleaners

I think some clarification might help, polo.

Are you saying the US cleaner cycles between low amplitude and high 
amplitude, or switches between two different oscillator frequencies? 
The switching, whatever it is, you imply takes place at the 60 hz line 
frequency, which would certainly simplify circuit design.

Your use of the word 'phase' was just to refer to the two states the 
drivers switch between, right?

Sometimes you have to read a little deeper between the lines, Marshall. 
grin

Mike D.

 Ok, thanks for that info, but nevertheless, this tidbit does not change
 the fact that ultrasonic cleaners are designed to have a low and high
 phase. How can a liposome be immune from rupture, by the tough
 phospholipids membrane when compared to the ordinary bubble??
 
 doug
 
 
 - Original Message - 
  50/60 Hz is the line frequency the unit is specified to work with,
  what comes in the power cord.  That is on the low end of the audio
  spectrum, not the high.  Cleaners typically run between 20 and 30 KHz,
  which is above the range of hearing. The movement is basically
  sinusoidal, thus the amount of time above the baseline is equal to the
  amount under the baseline.  The word phase in such a situation would
  refer to the difference in the angle between two waves and does not
  apply to these cleaners at all.
 
 
 --
 The Silver List is a moderated forum for discussing Colloidal Silver.
   Rules and Instructions: http://www.silverlist.org
 
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 List Owner: Mike Devour mailto:mdev...@eskimo.com
 
 

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[mdev...@eskimo.com]
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