P.S. Wikipedia's definition (in blue below) is consistent with what I remember.


A catalyst is a substance that speeds up a chemical reaction, but is not 
consumed by the reaction; hence a catalyst can be recovered chemically 
unchanged at the end of the reaction it has been used to speed up, or catalyze.



On Nov 26, 2015, at 2:13 PM, Ludwik Kowalski wrote:

> I also responded to Peter G, essentially at the same time. Bot my reply 
> bounced back. I wrote:
> 
> 1) Peter wrote (see his egoout below ): ... "I have a cult for catalysis, met 
> it professionally in many forms and have developed a kind of philosophy of it 
> ... .
> 
> I have a cult for catalysis, met it professionally in many forms and have 
> developed a kind of philosophy of it.
> 
>  - I claim a "catalytic" surface consists of nano-cracks. "
> 
> 2) I am not a chemist. But I would say that a catalytic surface is a surface 
> covered with one or more catalysts  (chemical compounds). Such compounds can 
> participate in reactions but are not consumed by these reactions). Some 
> chemical reactions would be very rare, if catalysts were not available.
> 
> 3) Does my definition conflict with Peter's nano-cracks definition? Probably 
> not; Peter probably thinks that some catalysts are present in nano-cracks. 
> Which compounds does he have in mind, in our CMNS context?
> 
> Ludwik Kowalski (see Wikipedia).
> 
> 
> 
> 
> 
> On Nov 26, 2015, at 2:05 PM, Edmund Storms wrote:
> 
>> a) Continuing discussion with Ed Storms
>> 
>>  Yesterday Ed has promptly answered to my catalysis in LENR questions, but 
>> has forgot to answer to this question "caused "by the unique PdD et classic 
>> paper of JCF-16 so I repeat it:
>> 
>> - what do you think about paper of Numata-  No.15 at JCF- see the  list? I 
>> have spoken more times about nano-vortices as NAE to you, in this is 
>> something like that
>> 
>> Ed: I will be pleased to comment once the paper becomes available.  If you 
>> you have a copy, please send it.
>> 
>> Ed's answer, my comments 
>> 
>> 
>> To answer your questions, we need to know what the words mean. The word 
>> catalyst describes a general concept, there being hundreds of different 
>> kinds of catalyst. One kind does not take the place of another. Simply 
>> saying a catalytic surface is required is too trivial.  What is worse, the 
>> concept of catalyst was only applied to a chemical reaction, never to a 
>> nuclear reaction, until LENR was discovered.  We need to know what the word 
>> means when it describes a nuclear process. A catalyst can reasonably be 
>> understood to lower a barrier by a few eV but what allows a barrier of 
>> several MeV to be lowered?
>> 
>> ANSWER 
>> Please, please read my essay here:
>> http://egooutpeters.blogspot.ro/2014/12/the-most-fundamental-question-about-lenr.html
>>  
>> I have a cult for catalysis, met it professionally in many forms and have 
>> developed a kind of philosophy of it.
>> 
>> Ed: I read your comment but I do not understand how it applies to our 
>> problem. A catalyst is a concept applied when the rate of a chemical 
>> reaction can be increased by operation of another chemical condition. To be 
>> useful, the chemical condition needs to be identified. This requires 
>> identification of the chemical state causing the rate of LENR to increase. 
>> In addition, we are faced with the need to increase a reaction rate having a 
>> barrier of MeV.  You have not answered my question. How can this be done?
>> 
>>  - I claim a "catalytic" surface consists of nano-cracks. These cracks are 
>> created by stress relief.  Many ways exist to create the stress and the 
>> resulting crack formation depends on the property of the surface.  Stress 
>> generation and crack formation are influence by many variables. We will not 
>> understand these variables until they are study for the purpose of causing 
>> LENR.  So, simply saying a catalyst is necessary without showing the form of 
>> the catalyst is useless.  Also, complaining about lack of knowledge about 
>> the process without showing what needs to be studied is also useless.  I'm 
>> attempting to show exactly what needs to be studied and what will be found 
>> when that study is undertaken. I see no one else doing this. Instead, we are 
>> provided with guesses and speculation based on what Rossi might wish to 
>> reveal. 
>> 
>> ANSWER
>> As far I know/understand, the nanocracks are not a specific, quantifiable  
>> feature of the metal (Pd, Ni) surface- with concrete it would be different. 
>> 
>> Ed: Peter, I'm amazed you would say this. The nano-crack is the initial 
>> formation of a gap that, if allowed to grow larger, would be and is easily 
>> seen.  This is a well known and easily observed process.  I'm not suggesting 
>> a new condition. I'm only suggesting a new consequence of a well-known 
>> condition. 
>> 
>> 
>> It is difficult to explain- based on the density of nanocracks per surface a 
>> thousand times increase of the heat release from PdD to NiH at 1200 C- the 
>> best for you is to deny it temporarily- an 1000 times increase of nanocracks 
>> density is not possible. We like it or not, cracking is a destructive 
>> process. My alternative is the dynamic formation of the NAE surfce 
>> nanostructures
>> due to the increased mobility and re-arrangements of surface atoms of the 
>> metals, obviously increasing with temperature.
>> 
>> Ed: What kind of nano-structures are able to initiate a nuclear reaction? 
>> You need to be specific.  What exactly needs to be created on the surface to 
>> cause LENR and how can this be done? I have answered this question using my 
>> theory. Can you give an answer using your understanding?  Making general 
>> comments is not useful at this stage. We need exact descriptions and 
>> predictions.
>> 
>> - Axil and others suggest treatments that would apply stress even though he 
>> does not explain the process this way. However, no one has the money or 
>> interest in setting up a complicated method without assurance that it has a 
>> relationship to creating the required conditions. 
>> 
>> ANSWER 
>> AXIL will explain this again, in more detail- please appreciate that AXIL 
>> tries to develop a holistic understanding of the field that is indeed very 
>> rich and varied.
>> 
>> Ed: Yes, but Axil's approach is too rich and varied. It is like throwing a 
>> collection of colored paint against the wall and hoping to form a picture of 
>>  something recognizable. I call this an abstract art form, not science.  We 
>> need to have exact descriptions that can be easily tested and related to 
>> what is presently known.
>> 
>> The essence of the problem is the lack of agreement about a NAE being 
>> required. Without this agreement, no one even looks for the NAE or attempts 
>> to identify it. I suggest a very plausible NAE, but this idea is ignored 
>> because the basic need for a NAE of any form is not accepted. 
>> 
>> Dear Ed, have you seen this jCF-16- how does it consider NAE:
>> What is the "nuclear active environment" of the cold fusion Tetsuo Sawada
>> LENR poly-semantics.
>> 
>> ANSWER
>> 
>> As regarding me, I have pre-agreed with NAE much before even the 
>> word/acronym was created by you just I called it "active sites" because they 
>> are fisrt topological and and only then environmental. I don't think they 
>> are nano-cracks in the surface but nanostructures on the surface. Is this  
>> an essential difference? ok- void space vs structured nano-matter, in the 
>> surface vs. the surface , static-preformed vs. dynamic, permanent vs. 
>> transient, possibly usual nuclear two particles reaction vs. collective 
>> transformation, fusion vs more complex nuclear interactions etc.
>> 
>> Ed: You and other people do not understand what I mean when I use the term 
>> NAE. It is not simply a site where LENR happens to take place, as you define 
>> it. It is a special local condition that is created by a chemical process 
>> BEFORE LENR can take place. Its eventual use as a site for a nuclear 
>> reaction is not anticipated by Nature when the NAE is formed. The nuclear 
>> reaction is an unusual and unexpected consequence.  For reasons having 
>> nothing to do with the eventual nuclear process, this condition forms and 
>> allows something extraordinary to happen. This way of looking at the problem 
>> forces an entirely different set of rules on how the process works.  You are 
>> free to reject my idea, but please understand what I propose before you 
>> reject it.  You and I are describing an entirely different condition when we 
>> use the term NAE.  I do not believe your definition applies because I do not 
>> believe a process that can cause fusion can take place in or on a normal 
>> material.  A very unique and rare change must take place. We need to 
>> identify this change in an exact way while remaining consistent with known 
>> behavior.
>> 
>> Further- is NAE a chemical structure and are you right as you say:
>> The chemical structure of a material has to be modified in a unusual way 
>> before LENR can be initiated. 
>> Or is it about dimensions first i.e. is it a nano-effect primarily.
>> 
>> Ed: OK, that comment is the start of an agreement. As for your question, I 
>> have no idea what you are asking. We know that no matter what happens, it 
>> must take place at a nano scale. We have a very limited number of possible 
>> changes that can take place in a material at this size level.  Exactly what 
>> kind of change do you propose?
>> 
>>  I forgot to ask- what arguments do you have for the existence of hydrotons 
>> Are they active somewhere?
>> 
>> Ed: In order to fuse, the hydrogen MUST occupy the same place at the same 
>> time.  For the sale of discussion, I use the word Hydroton to identify this 
>> assembly of hydrogen.  I propose how it forms so as to be consistent with 
>> the rules of thermodynamics. I speculate that metallic hydrogen would have 
>> the same ability to support a fusion reaction, hence could be called a 
>> Hydroton. 
>> 
>> 
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