I've noticed a tendency for the synthetics with the lowest NOACK to post higher TEOST Deposit numbers and vice versa.
Can someone explain the likely reasons why?
Can someone explain the likely reasons why?
"Heavier" oils are less volatile, but are more prone to leaving more carbon residues and don't solubalize carbon as well as "lighter" oils.
"Lighter" oils are more volatile, and help solubalize carbon deposits as they form and also contribute less to deposit formation.
Just typical trade-offs when selecting base oils.
"Heavier" oils are less volatile, but are more prone to leaving more carbon residues and don't solubalize carbon as well as "lighter" oils.
"Lighter" oils are more volatile, and help solubalize carbon deposits as they form and also contribute less to deposit formation.
Just typical trade-offs when selecting base oils.
This answer was better.I think your answer lies in the presence of esters or lack thereof.
I've noticed a tendency for the synthetics with the lowest NOACK to post higher TEOST Deposit numbers and vice versa.
Can someone explain the likely reasons why?
In in-house high temperature, thin film deposit tests that my former company ran regularly, PAO and Group III based oils always left more deposits than Group I or ester based oils. The lack of polarity/solubility of these higher group hydrocarbon base stocks meant they were not able to solubilize or disperse oxidation by-products that lead to deposits. Pure ester based oils were always the cleanest by far, and had the lowest Noacks by far.
That said, our test oils were industrial and aviation products that did not contain detergents or dispersants, which can influence such tests, and we never attempted to establish any correlation between our test and the TEOST test. The solubility principle, however, may still apply.
Like I said, I think your answer lies in the presence of esters or lack thereof. I just gave the short version.In in-house high temperature, thin film deposit tests that my former company ran regularly, PAO and Group III based oils always left more deposits than Group I or ester based oils. The lack of polarity/solubility of these higher group hydrocarbon base stocks meant they were not able to solubilize or disperse oxidation by-products that lead to deposits. Pure ester based oils were always the cleanest by far, and had the lowest Noacks by far.
That said, our test oils were industrial and aviation products that did not contain detergents or dispersants, which can influence such tests, and we never attempted to establish any correlation between our test and the TEOST test. The solubility principle, however, may still apply.
It's Noack, named after Kurt Noack. Not NOACK.
Had these tests been run at common temperatures around the 275-300°C? One of the remaining questions (if looking beyond 33c and MHT) would be, how far their window of nasty behaviour may have shifted ;-) Depending on application or exact focus it wouldn't necessarily mean much difference around the rings or via premix, metering oil pump or else.
Ketjenlube polymer esters once had been presented as if they were first to be allowable right into combustion chambers and Croda of 21st century depicted some POE as admirable while Idemitsu heading for some Le Mans of 20th century still avoided them – because of engine tests of course, but also over accompanying thin film coker testing.
Croda ran the coker tests at 275°C, Idemitsu at 280°C – so much transparency's already in it. TEOST 33c specifically aiming at turbo shafts has more heat but no air. So, please don't hesitate to give any longer versions. Despite not much ester content to be expected in most of the oils around, if I don't get Gene K totally wrong.
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