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8:02 PM
Hi all, I have a question about observables and the absolute value
I am considering an expectation value of a density operator of some system, and it appears as though taking the absolute value prematurely gives the wrong results
Why is this? I always thought the absolute value may be considered distributive
It also seems as if taking it prematurely makes the system non-integrable
 
@1010011010 I'm not sure what you mean by "distributive", but $\langle \lvert A\rvert\rangle \neq \lvert \langle A\rangle \rvert$.
In other words, you need to be clear whether you want to take the absolute value of the expectation value or the expectation value of the absolute value; those are not the same thing.
 
Certainly, though suppose my density operator is given by two factors, certainly one would expect the absolute value of the 2 state matrix element to be the absolute value of the individual factors, no?
In technical terms $\lvert <\hat\rho> \rvert = \lvert A\rvert \cdot \lvert B\rvert$, where $A$ and $B$ are those two factors
It appears as though in my system these two factors "communicate" for the lack of a better wording, or so the math suggests
 
I don't understand how the "two factors" are supposed to be related to $\rho$
 
Oh, sorry, ok, so basically the quantum operator is calculated between two states, which I'm calling a matrix element of the state space, so the matrix element could be $<\Psi|\hat\rho|\Phi>$ for any two states psi and phi
 
I know what a matrix element and a density operator are, I do not know what "my density operator is given by two factors" means.
 
8:12 PM
Ok suppose the expectation value is given by a product of two functions, $f(x)g(x)$ both of which are allowed to be complex
Though it is not necessary that they are
 
What's $x$, and why would an expectation value be complex rather than real?
 
If I calculate the absolute value of this matrix element, why can't I just say it is equal to $|f(x)|$ times $|g(x)|$
Where $x$ is an otherwise indeterminate system parameter on which $\rho$ depends
 
$\lvert f(x) g(x)\rvert$ = $\lvert f(x) \rvert \lvert g(x)\rvert$ is rather trivially true - you'll have to describe more precisely what you're doing here and how your result differs from that.
 
I calculated my density operator of the 1d bose gas by the conventional method and by using that identity I too thought was trivial (using the absolute value in that way) and by keeping all the phases
If I keep the phases and use a geometrical argument, parts of the expression become Dirac deltas after the thermodynamic transition
This imposes constraints that don't seem to be there when I use that rule
 
Oh, there's a limit involved! It is not true that $\lim_{x\to a} \lvert f(x)\rvert = \lvert \lim_{x\to a} f(x)\rvert$
(just consider the function that is +1 on the rationals and -1 on the irrationals to see that, or the alternating sequence -1,1,-1,1,-1,1,...)
 
8:21 PM
What is the condition for it to be equal?\
Is it correct for a root of some function? Or for a simple rational product?
 
@1010011010 If $\lim_{x\to a}f(x)$ exists, then $g(\lim_{x\to a} f(x)) = \lim_{x\to a} g(f(x))$ for any continuous function $g$.
But the fact that you are talking about $\delta$-functions there makes me suspect these limits do not rigorously exist
 
Good point. In this case they are the result of a limit though
 
8:38 PM
I have made a plan and will start with the derivation of the two state matrix element to see if the absolute value is already applied, that would explain a lot
Thanks
 
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