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Testing Coolant: Basic Question
I have a basic question related to testing my coolant.
My understanding is that coolant needs to do four things: transfer heat, prevent corrosion, not boil, and not freeze. I have a basic hydrometer that tests only the freeze point. My question is: can I assume the the properties of a coolant, its abilities to do what it's supposed to do, deteriorate at approximately the same rate? So that, if the freeze point is still very low, I can assume that the boil point is still high and the corrosion prevention still intact. Or conversely, is it possible that the deterioration of the properties will occur at significantly different rates? Thanks. |
antifreeze has little to do with the boiling point protection. the cap does that. higher pressure caps boil water at a higher boiling point.
PURE water will boil slower than water with antifreeze in it. the water wetter products reduce the water particles and make it absorb heat faster... keeps the motor cool. |
Hydrometer tests amound of dissolved stuff in coolant. Freeze and boil temps are dependant mostly on that. As vstech points out, pressure held by cap is predominant boil temp control.
Corrosion protection is via chems in antifreeze, and they get used up over time, hence the periodic repacement. Expect corrosion protection to degrade nearly independently from hydrometer reading. |
If I wanted to test corrosion protection, how would I do that? With one of those little strips?
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A rule of thumb is that for every PSI an automotive cooling system is pressurised the boiling point temperature is increased by one degree Celsius...
Read more than you'd ever want to know about antifreeze here:- http://en.wikipedia.org/wiki/Antifreeze |
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Generally the high boiling point of water and its high heat capacity is due to the hydrogen bonding between molecules. However, Tango, you are correct that the addition of antifreeze increases the boiling point of water. This is due to the colligative properties of mixtures and the fact that anti-freeze has a higher vapor pressure than water. The addition of anti-freeze increases the overall boiling point, despite reducing the hydrogen bonding of the water molecules. I hope no one minds my geeking out here. http://www.peachparts.com/shopforum/images/icons/icon10.gif |
Never Assume ANYthing WHEN :
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You use a VOM to check the corrosion protection ( as per the FSM )... |
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Incorrect. Anti-freeze does not significantly alter hydrogen-bonding. Incorrect. The size of these molecules size does not appreciable change because of the presence or absence of inter-molecular forces from other molecules. ------------ |
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You can buy a kit with test strips to test coolant, I keep them on-hand for testing. They are diesel-specific, the simple 3-way test: pH, Nitrates, and freeze-point, there are also 5-way strips.
The problem is that I don't know if these are accurate to the needs of a Mercedes-Benz automobile, so even if they indicate good there might be something that Mercedes diesels need that isn't being tested (or indicated to the proper Mercedes level). The kits only have about a 1-year shelf life, less than the life of the coolant in your car so if you do wish to play with the strips buy the 3-strip packet from NAPA instead of the more common 50-strip bottle$. The easiest IMO is to just change at the factory interval with the proper G-05 coolant and distilled water (per FSM). On the 124s there is a new pressure tank available that has a silicate pack in it (aka: coolant filter in the H-D world) to extend the useful life of and stabilize the diesel coolant, I don't know if the same is available for your 126. |
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The "cavitation inception" I have heard of described as a nucleation source. That's why we put boiling chips in a beaker to control the boiling. It is an entirely separate process than the colligative mechanism discussed above. |
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I do not know how one would directly measure increased or decreased hydrogen bonding. I do not know if the IMF (inter-molecular force) of hydrogen-bonding (it's not a bond but an interaction) is measurable with spectroscopy. It's not an area that I have explored. So I am not aware of anyone showing an increase/decrease in hydrogen bonding by doing such-and-such. Surface tension is a surface phenomena. It is understood by the presence or absence of certain chemicals that are at the surface. The term surfactant means surface active agent. It's very possible to add a chemical to water and have it present in the part per million level in the solution and yet be a thousand (or more) more concentrated at the surface. I believe I understand the thinking of the statement: .. decreased surface tension indicates decreased hydrogen-bonding ... It is not an accurate description of what is occurring. Sorry. It's not a personal attack I've just spent a lot of time studying inter-facial phenomena. Quote:
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That's interesting. I wonder with the difference in AF composition today versus when the FSM was written if that is still valid. Could you briefly describe the FSM procedure and values? Thanks. |
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