Used this example before, but if you tried putting your hydrometer into a trial jar of porridge im sure you'd get a pretty high reading

I believe the second bold red word is what you meant?UserDeleted wrote:
Hydrometers work on the principle that a molecule has the ability to turn polarised light in a given direction by a given amount. for each molecule this is known, and instruments can be calibrated to this particular level. Of course there is some interaction between molecules (hence the fuzzy line), but in general they can be pretty specific. Although I do know one homebrewer who uses a refractometer calibrated to read urine and a lookup table to convert back to maltose / brix
Oh and its a $300 refractometer!!
Lets not even consider a mixture of laevorotatory and dextro rotatory molecules
"It's better to be a fool for 5 minutes of your life by asking a question than to be a fool for the rest of your life by not knowing the answer"SteveD wrote:You just did.mr.c wrote:Just read the posts,so am i going about it in the wrong way
? eg "take a sample of the wort and cool it down to 20C and take a hydrometer reading,can some one summaries it up for me plz how do you do it?
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UserDeleted wrote:Its quite simple really. Take your hops at the end of the boil and squeeze them out into a jug. Pour that into your hydrometer sample jar and take the gravity. Remove the hydrometer and let it settle. Add the hydrometer again and it will get stuck in the break material.
In short If it is in the hydrometer jar it will affect the reading on the hydrometer, which simply shows the relative difference in weight between your sample and a sample of water.
Hydrometers work on the principle that a molecule has the ability to turn polarised light in a given direction by a given amount. for each molecule this is known, and instruments can be calibrated to this particular level. Of course there is some interaction between molecules (hence the fuzzy line), but in general they can be pretty specific. Although I do know one homebrewer who uses a refractometer calibrated to read urine and a lookup table to convert back to maltose / brix
Oh and its a $300 refractometer!!
Lets not even consider a mixture of laevorotatory and dextro rotatory molecules
Go out to your garden get a handful of soil put it in some water and shakeSteveD wrote:It seems logical to me, and there must be something writen about this, but it's the weight of the liquid that the hydrometers measure. Assuming it's not physically resting on break material, or otherwise being obstructed, the weight of solid floating about in the liquid being measured is irrelevant. The only time it might matter is if the solid had precipitated out of the solution being measured.
Example :- Take one large test jar. Fill it with sugar solution. Take the OG, say 100. Then drop a quantity of inert sand into it. Take OG again. I can't see how it can be anything other than 100 again.
If on the other hand if the solid precipitated out of the solution eg trub or sugar crystallising out, the reading would go down, right? But would it?? If the volume stays constant, you'd say yes. But I don't think it does. As the solid precipitates out, does the volume of liquid not reduce as a result? Reduced volume increases the concentration of the remaining liquid, possibly negating the effect of the precipitation and resulting in a reading that does not perceptibly change.
Note, This is all just my opinion. I haven't read anything about this anywhere.