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user228700
09:01
^ Yes, it really would. My exam isn't until April, but I've to write practice exams so I need to finish the syllabus by the end of December.
user228700
@JohnRennie Thing is, Sir, this past summer was tremendously painful for me, because of consistently failing to pass the exams that then lead to other personal problems. I've gots to do better next year. So the rushing.
I guess the thing to do is just stick with the syllabus for now. I just hope it doesn't put you off physics for life :-)
user228700
It certainly won't :-) I've learned more in these past months than I have in the past two years, that's for sure. Well, at least I've had more fun doing it.
Mew
Mew
she wants to be a physicist of rcourse she won't be put off
user228700
:-) Idk what I want to be but "physicist" doesn't look so bad. It has never looked bad...
Mew
Mew
09:10
what about doctor?
user228700
Nope. Didn't take Biology in High School.
Mew
Mew
cool that would be a bad job
user228700
:-P I'ma do physical chem. for awhile, before switching back to Electrostatics.
Mew
Mew
yeah k imma go play a game
user228700
Have fun :-)
user228700
09:22
@JohnRennie: Approximately how much time dyou reckon it will take to tell me about:
user228700
yesterday, by John Rennie
The spectre of Gibbs free energy floats into view ... :-)
user228700
It's been nagging me ever since and I'm studying about the elevation of boiling point due to the presence of a solute, which makes it worse.
user228700
Dyou reckon it'll take an hour at least? If so, I might as well just skip it...
The trouble is that I can't tell you just about Gibbs free energy. I'd also have to explain enthalpy and entropy and we'd end up discussing pretty much all of thermodynamics.
However I can talk in general terms about how to understand processes in terms of the Gibbs free energy.
user228700
That's OK. Dyou think it'll take long? Just to explain about the boiling point.
user228700
09:26
(Given that now u have a rough idea about how looong it takes me to wrap my head around new concepts)
Well the basic principle is that a process occurs spontaneously if the change in Gibbs free energy is negative.
That is the total Gibbs free energy of the products is lower than the total Gibbs free energy of the initial system.
user228700
Yes, of course...
It isn't that different to the basic principle that everything settles into the lowest energy state.
user228700
Okay...
user228700
Let's stick only to boiling point. U said:
user228700
09:28
yesterday, by John Rennie
Don't worry about the vapour pressure. That's related to why there is a boiling point (and it's to do with the free energy). The boiling point is defined as the division between the liquid and vapour ona phase diagram.
The thing about Gibbs free energy is that it includes entropy as well as energy. So you need to think about the entropy changes involved in any process.
user228700
OK...
@Kaumudi OK.Do you want to talk about boiling of a pure liquid, or why a solute increases the boiling point - or both?
user228700
We could talk about the latter-that way, we'd sort of end up covering both, no?
user228700
I will tell u how I understand the concept: when solute molecules are dissolved in the solvent, the surface now contains some of these too. Hence, not all the solvent molecules are able to vaporize as before. Therefore, the vapour pressure of the solvent decreases.
09:32
Suppose you're considering boiling of a liquid, then the initial free energy is the free energy (per mole) of the liquid and the final free energy is the free energy (per mole) of the vapour.
user228700
Since the vapour pressure has decreased, and the boiling point is defined as that temp. at which the vapour pressure becomes equal to the "external pressure", more heat must now be added to the system to achieve this equality. Hence, the boiling point increases.
user228700
Is my understanding at least "OK"?
We need to put energy in to vapourise a liquid, the latent heat of evaporation, so in the equation $$\Delta G = \Delta H - T\Delta S$$ the enthalpy $\Delta H$ is positive.
user228700
Right.
But that tends to make $\Delta G$ positive, which opposes vapourisation. That means vapourisation only happens because the entropy change $\Delta S$ is large. A large $\Delta S$ means $-T\Delta S$ is large and negative and it outweighs the positive $\Delta H$.
user228700
09:35
Don't u mean "large and positive"?
Now suppose we add some salt to the water.
user228700
Since the term is being subtracted...
@Kaumudi oops yes.
user228700
@JohnRennie OK...
Anyhow, adding salt to the water doesn't change the vapour because the vapour is still just water vapour. So when we look for the reason the BP rises it must be a change in the water. Yes?
user228700
09:39
Uhh, I can't agree with u right away, but do go on...
@Kaumudi we should probably check why you're not sure about this before proceeding ...
user228700
No, I'm pretty sure that I'll understand what u mean when I understand why the change in water is causing this change in BP. I don't exactly understand what u mean by that. If u proceed, I think I will. I'll shout if I don't :-)
OK. Remember that the free energy change is $\Delta G = \Delta H - T\Delta S$.
The $\Delta H$ is basically just the energy we need to put in i.e. the latent heat of vapourisation.
user228700
@JohnRennie That equation has been imprinted onto my brain, I will never forget it! :-)
user228700
@JohnRennie Yes...
09:43
And in fact the latent heat of vapourisation (as measured by experiment) of salt solutions is almost independent of the salt concentration.
Mew
Mew
@JohnRennie can you derive the equation pls
user228700
@JohnRennie That fact is an "Eff you" to the explanation that my textbook uses, is it not?
I guess the reason for this is because for a few percent of salt most water molecules are still surrounded mostly by other water molecules, so the energy needed to pull a water molecule out of the bulk doesn't change much.
So if $\Delta H$ doesn't change much that means the boiling point elevation must be due to a decrease in $\Delta S$.
user228700
Wow. Okay...
If $\Delta S$ decreases then that means $T\Delta S$ decreases, so we have to increase $T$ to keep the product $T\Delta S$ constant.
And increasing $T$ is of course exactly what we mean by the boiling point going up.
So far so good?
user228700
09:48
@JohnRennie Hang on. I don't understand why $\Delta S$ has to decrease...
user228700
Gimme a minute to think it through, please.
@Kaumudi I'm arguing that if $\Delta S$ decreases then $T$ must increase to keep $\Delta G$ negative.
user228700
Yes, but why does $\Delta S$ decrease?
So the converse is that if we see the boiling increase (which we do), and $\Delta H doesn't change, that implies $\Delta S$ is decreasing.
user228700
Yep, OK.
user228700
09:50
(I thought there was some other physical reason...is there?)
$\Delta S = S_{gas} - S_{liquid}$. Yes?
In other words the entropy of the final state minus the entropy of the initial state.
user228700
Yep.
And the entropy of the vapour doesn't change (much) because whether we have salt in the liquid or not the vapour is just water vapour. So that means the change must be due to an increase in $S_{liquid}$.
The entropy of the water must go up when you add salt to it.
user228700
Oh, right.
user228700
Because the salt molecules take up some space that was previously available to them?
09:54
So we need to understand why the entropy of water goes up when we add salt to it.
Entropy has a precise definition that unfortunately is hard to understand, but a common handwaving definition is to say that it's a measure of disorder.
user228700
Is my reasoning correct?
@Kaumudi not really, or at least that isn't the way I would describe it.
user228700
:-( OK...
Pure water is relatively ordered because everywhere you look is just water.
user228700
^ That doesn't make a lot of sense to me .___.
Mew
Mew
09:57
na water is very entropic
But when you add salt to it you now have a mixture of molecules, so if you look at any random point in the liquid there could be water there of there could be salt there.
So in a vague arm waving way salt solution is more disordered than pure water. So its entropy is higher.
user228700
^ That is the most arm-wavy explanation that u have given me.
Mew
Mew
I agree salt+water is more disordered than water
there are more possible states in the salt+water system than in the water system alone
and entropy is proportional to the number of possible microstates
@Kaumudi because defining the entropy of a liquid, and a liquid solution is mind manglingly complicated. Arm waving is the best I can do.
user228700
Hmm, OK.
user228700
09:59
So that's why the boiling point increases.
user228700
God, it appears exactly as if high school is setting up students for quite a lot of hair-pulling and head-desking once they get to college.
user228700
My textbook explained this by saying that $\Delta H$ increases.
user228700
Sorry for the timeout - phone call ...
user228700
That's OK :-) Alright, what about this boiling point itself, then?
10:05
@Kaumudi Where does that say $\Delta H$ increases?
user228700
Oops, hang on:
user228700
user228700
I guess they haven't exactly spoke about the increased $\Delta H$, after all. They've spoken about the surface area...
There are always two ways to approach things like this this. One way is the microscopic approach i.e. you think about what happens to individual molecules.
And the other is the macroscopic approach i.e. you think about bulk properties like entropy and enthalpy and you don't worry too much about exactly what happens on the micro scale.
user228700
Right .___.
10:16
What I've done here is talk about the macroscopic approach. So I've said the entropy increases and I've waved my arms around when you asked why the entropy increases.
Your book is trying to justify things with a microscopic approach.
But to honest the book's microscopic approach is pretty arm waving as well :-)
user228700
:-) Yes. Alright, dyou have the time to explain about boiling point, real quick?
Yes OK.
The entropy of an ideal gas depends on the pressure in a scarily complicated way
But all we need to know is that as the pressure goes down the entropy goes up.
So as we decrease the pressure of the gas the free energy also decreases.
user228700
WHICH PRESSURE?!
If it's a pure gas then it's just the regular pressure. If it's in a mixture, e.g. water vapour in air, then it's the partial pressure.
Clear?
user228700
@JohnRennie I'd figured the opposite, actually, but OK...
user228700
10:22
@JohnRennie How are we doing the decreasing, exactly?
@Kaumudi well, consider this. If we leave a gas to itself its pressure will decrease. That is, if we put a lump of gas in a vacuum the pressure goes down and the gas expands.
That means the free energy change for the expansion must be negative.
Mew
Mew
IF you apply so much pressure to a gas that it turns into a solid, it has become more ordered and entropy has decreased
And that means the free energy must fall as the gas expands and its pressure goes down.
user228700
@JohnRennie I see...
So the free energy of a very dilute gas is lower than the free energy of a higher pressure gas.
user228700
10:24
@JohnRennie Uhh, one second...
user228700
@JohnRennie Alright...
Suppose we start with liquid water at 0C. To form water vapour we need to put a lot of heat in and that makes for a large and positive $\Delta G$.
So water can only vapourise if there is a very large and positive entropy change.
And the water vapour can only have a very large entropy if it's very dilute i.e. if its partial pressure is very low.
And the partial pressure of the water vapour is just the vapour pressure of the liquid water. So we conclude that the vapour pressure is going to be low at 0C.
user228700
::scratches head violently::
Consider the change water -> water vapour
For this change we have $\Delta G = \Delta H - T\Delta S$
user228700
OK, no, Sir, let's let it be. I think my head might just burst any time now.
10:30
OK :-)
As I said, it is a bit of a distraction.
user228700
Thank you :-) _/\ _
user228700
@JohnRennie I wonder what counts as "distraction" to u...(?)
Is the emoticon a namaste?
user228700
Yes! Well, in this case, it signifies "dhanyavaad" =Thanks.
@Kaumudi my exams are far, far behind me. These days I'm free to pursue any distractions I want. And jolly good fun it is too :-)
user228700
10:33
@JohnRennie Quit bragging :'-(
You too will one day be in the same position. Of course the downside is that you too will be middle aged by then! Life's like that :-)
user228700
:-)
user228700
Alright, gots to go eat s'thing. Dang it, we're out of oranges!!! >.<
11:14
@JohnRennie what's wrong with middle age?
31 is nice: I'm trained professionally, financially independent...
I can spend money on chocolate as I see fit!
3
@DanielSank Nothing. I am thoroughly enjoying a disreputable middle age. However experience suggests that the ladies are less keen on being middle aged.
@DanielSank Incidentally, Bernardo asked if I could set up a play server for his experiments with rust, and I've done this. Do you want the details? NB it's a Server 2008 installation. I feel uneasy hosting a Linux server because i don't know it well enough to be sure it's secure.
@JohnRennie yes please. If you want to email, you can find my contact info through my profile.
I don't promise not to pwn you though...
@DanielSank e-mail on the way. If the FBI come calling remember I know where you work :-)
11:25
@JohnRennie :|
Rust is weird. Have you tried it at all?
I compiled a HelloWorld sample to check the Rust compiler had installed correctly. Apart from that I haven't looked at it. It looks superficially very like C++.
How can 2008 software be secure?
@JohnRennie hmm, no classes though!
I feel like I've used a dozen languages over the years and apart from the outliers (LISP) they are all much the same. The key thing for using a language is the availablity of libraries.
Yes, libraries are why Python is so useful.
C++ has the huge advantage of a massive code base, and C# has the huge MS supported class library. Any new language has to compete with this.
@DanielSank yes, Python, has made the jump to critical library mass.
11:30
@JohnRennie Rust is definitely not competing with C++.
Rust is competing with C.
user228700
Can anybody help me w/ some organic chemistry?
Why would anyone try and compete with C? Who uses C for anything but legacy work these days?
user228700
@JohnRennie !!???!
Git is written in C!
Operating systems are written in C.
user228700
^ Which of these two structures is more stable?
user228700
11:33
in The Periodic Table, 6 mins ago, by Kaumudi
I vote (b), because it looks like both structures have the same number of $\alpha$ hydrogen atoms and trans is more stable than cis, correct..?
@DanielSank if you were writing a new OS now, why would you choose C over C++?
@Kaumudi Do the two isomerise? I can't see an obvious mechanism.
Or do you mean which has the lower heat of formation?
@DanielSank I didn'tknow git was written in C. That seems a strange decision. I can't see what possible advantage you get from using C rather than C++.
user228700
@JohnRennie No, I don't think so. I'm supposed to predict their relative stabilities in terms of effects such are resonance and hyperconjugation.
@Kaumudi I don't know what that means. What is the actual question in your book?
user228700
Don't know. Sorry :-(
user228700
11:39
OK :-( I'll wait to see if anybody responds at The Periodic Table.
user228700
I posted a question on CSE almost a week ago and I've received literally no answers yet >.<
user228700
1
Q: Is the inductive effect always measured relative to hydrogen?

KaumudiWikipedia has defined the Inductive effect thus: "In Chemistry and Physics, the inductive effect is an experimentally observable effect of the transmission of charge through a chain of atoms in a molecule, resulting in a permanent dipole in a bond." Recently, I learned from a teacher that t...

user228700
Can anybody help me to choose the correct option as to why I'm starting a bounty?
user228700
It looks like most of them apply in my case :-/
user228700
What is a "Canonical answer"?! :-|
11:44
@JohnRennie Linus tornados CV me r THIS
user228700
There. Started a bounty.
@DanielSank Torvald's views on C vs C++. Well, he's a better programmer than me. But I can't help feeling this is all down to design skills rather than language features.
@BernardMeurer you have mail (on Facebook)
Goddammit I have a huge test today and I couldn't sleep
user228700
@SirCumference: :-( All the best for ur test, man.
@Kaumudi thanks
11:49
Yes, good luck!
I'll just need coffee I guess
@JohnRennie C++ has a huge disadvantage of being unsafe. Its extremely easy to shoot yourself in the foot with C++.
@SolenodonParadoxus yes, but that's just as true of C.
@JohnRennie managed languages such as C# and Java have a huge advantage when it comes to safety
@SolenodonParadoxus yes, but the question is why Linus Torvalds should choose C over C++ for writing git and the Linux kernel.
11:53
@MAFIA36790 RIP obe
@JohnRennie ah I see
user228700
@SirCumference That's kinda...creepy.
user116211
@SirCumference ;_;
@SirCumference That's going to haunt me for the rest of my life :-)
4
11:55
@Kaumudi Almost as creepy as the vid above
user116211
Well, @sirC, we have fortunately added him in Skype; let's hope he comes in Skype.
user228700
Does anybody know why an $sp^2$ carbon in a 3 membered ring is unstable due to "ring strain"?
@JohnRennie Don't worry, we don't think you're an ASShole
user228700
Okay, the better question would be "Wtf is ring strain"?
@Kaumudi the sp2 bond angle is 120° while the bond angle in a three membered ring is 60°
user116211
11:57
Know about ring torsion?
user228700
@JohnRennie Ohh, right .__.
user228700
@JohnRennie Yeah, you're more like a God to me :-P
user116211
Did something actually happen with obe @SirC?
user116211
I didn't get his behaviour lately.
@MAFIA36790 No clue
Let's hope he'll come back when @0celo7 is back
user116211
12:00
@SirCumference hmm
Pretty harmless. Come on. Harmless. HARMLESS!!!
2
After more than 3 hours of trying to make sense of this question by another user, I have tied myself into knots. I am going to just go back to algebra because this is going nowhere
4
Q: How do you prove this very different method for evaluating $\sum_{k=1}^nk^p$

Simple Art I found the following formula in my previous question. This differs from my previous question in that I want an alternative proof of the below recursive formula for calculating $\displaystyle\sum_{k=1}^nk^p$. Suppose I had a function recursively defined as $$f(x,p)=a_px+p\int_0^xf(t,p-1)...

Recurrence relations are interesting, but the lack of ways to visualise the general case means it is very hard to probe for symmetries
@SolenodonParadoxus ???
not to mention I knew almost nothing on how integrals behave as an abstract linear operator
In the video that Sir Cumference posted
A guy tries to explain how his question is harmless
Made my day
12:02
@SolenodonParadoxus That video is kind of scary
@SirCumference Let's just say I'm quite pleased there is a large ocean between me and him :-)
2
He said evolution is physics
This is what I get when I substitute away all the integrals in the recurrence relation:

$$f_p-x\partial_xf_p+x^2\partial^2_xf_p=x^2p(\partial_xf_{p-1}+f_{p-1})$$

one sign short of being cauchy euler for the LHS!
@SolenodonParadoxus @JohnRennie He made a sequel
- The photon is described by QED
- That's what I'm saying - the photon is described by bullshit
Copenhagen made-up crap XDDD
I can't stop laughing
Seriously considering that it might not go away ever
In some individuals the feeling of self-importance knows no boundaries
It appears that the thought that he might not know all of it never crossed his mind
12:13
The belief that scientists deliberately make things complicated to conceal the truth from the masses is more widespread than you might think.
@JohnRennie You're a god
Have you attempted to log in? Does it work?
@JohnRennie I did, and I sent you a message on facebook saying I couldn't. I can ping the server, but I can't RDP into it nor can I telnet it
The only ports open are port 3319 for RDP and 6666-6669 for your chat app.
When you attempted to RDP did you specify port 3319?
@JohnRennie I did
12:24
@BernardMeurer that IP address is wrong.
OMG4
IT WORKS
It's fast!
@SolenodonParadoxus Why is he shirtless?
Am I the only one wondering that?
Dude is like a stereotypical caveman, complete with the accusation that physics is magic
C:\Users\Administrator>query user
USERNAME SESSIONNAME ID STATE IDLE TIME LOGON TIME
bernardo rdp-tcp#0 3 Active . 30/11/2016 12:25
administrator rdp-tcp#1 5 Active . 30/11/2016 12:25
It even has Powershell!
@JohnRennie You're a literal god
@BernardMeurer Only 2GB memory - that will be the limiting factor. That's the trouble with VMs. It's easy to get CPUs fast enough to handle lots of VMs, but buying enough memory is expensive.
12:28
@JohnRennie Last server we were using had 1GB :P
Anyhow feel free to play. I've left a folder on the desktop with various info in it.
As long as you don't try and compile GCC it works
hello everyone
To be fair 1GB goes farther on Linux than on Windows.
@heather do you want access to Bernardo and Daniel's play development server?
@heather hello (^ム^)
12:29
@JohnRennie, that would be cool, but I think the chances of me breaking something are a bit high =) what are they doing on it?
> what are they doing on it?
Playing :-)
=D that's awesome
So breaking it isn't an issue. Anyway i have a backup
okay. if they don't mind, then sure!
How do I get the user credentials to you without showing them in plain text here? E-mail? Facebook?
12:32
probably email, but its not in my SE profile
user228700
> Cyclonic storm ‘Nada’ heads towards TN coast, heavy rains expected in Chennai from Dec 1
user228700
Oh, crap.
@JohnRennie By the way, just wondering
@Kaumudi, hello =)
Why didn't you run for mod earlier?
user228700
12:33
Hey :-)
@heather E-mail me at [email protected] and I'll mail you back with the details.
@JohnRennie, okay =)
@JohnRennie It's not a problem until we break out of ring -1 and escalate our privileges and control your brain
@JohnRennie Ratsauce?
@BernardMeurer I have placed a potato restriction zone round the server :-)
2
12:34
Goddammit, my powers are useless now
Goddammit, that excruciating pain when you stub your toe so hard it bleeds
a potato restriction zone, lol
@JohnRennie, email: sent
Okay folks, I gotta head to class, I'll be back to play later tonight, catch y'all later
heather go check the github repo, it now has arbitrary precision
(The Collatz computer)
12:37
@SirCumference : FYI, the video refers to Phys.SE question #196812 (visible by 10k+ users only).
@heather you have mail
@Qmechanic Can't read it :/
@JohnRennie, thank you =D
@Qmechanic I know only 10k rep people can read it
Ain't one of those people
Screenshot?
@heather you'll need an RDP client. I'm pretty certain there will be one available for the Chromebook. Bernardo and Daniel can help if you run into problems.
12:42
@BernardMeurer, okay
@JohnRennie, oh, so it isn't something I install on the linux side of my system but on the chrome side?
@heather ah, I had forgotten your Chromebook dual boots linux. On linux I think the app is called rdesktop. See rdesktop.org
Hello, minds!
@SirCumference I know right
@heather I have absolutely no idea what incantation of apt-get installs rdesktop, though Bernardo will know.
i could use that, or i could use this which is for the chrome side...which would be better?
@JohnRennie, okay. =)
12:46
An RDP Chrome app will work fine, but it's $9.99 and rdesktop is free :-)
@SirCumference anyway it looks like he's on drugs
@heather Why not try the seven day free evaluation of the Chrome app and see how you like it?
@SwapnilDas Hi
oh, its 9.99, i hadn't noticed that...
Some questions on theoretical physics education, if someone cares to answer:
Does condensed matter theory take lesser time for PhD than GR?
Time is here average time.
And can both fields be related to one another, possibly?
12:50
@SwapnilDas no-one does PhDs in GR these days. It's too mature a subject. You might use GR in a PhD on cosmology or string theory or whatever but GR wouldn't be the main subject.
Doesn't GR have unsolved problems? @JohnRennie
On the other hand condensed matter is a booming subject and a PhD in it will make you highly employable.
@JohnRennie a fellow of mine did PhD in numerical relativity
@SolenodonParadoxus if it doesn't hurt you, could you tell me what's that?
@SolenodonParadoxus I can't comment. I just get the impression that post-docs in GR are few and far between.
12:52
And yes, any relation in the two fields?
@SwapnilDas it won't, but I don't think I can put it better then wiki
Numerical relativity is one of the branches of general relativity that uses numerical methods and algorithms to solve and analyze problems. To this end, supercomputers are often employed to study black holes, gravitational waves, neutron stars and many other phenomena governed by Einstein's Theory of General Relativity. A currently active field of research in numerical relativity is the simulation of relativistic binaries and their associated gravitational waves. Other branches are also active. == Overview == A primary goal of numerical relativity is to study spacetimes whose exact form is not...
Haha, was seeing that.
However, I agree with @JohnRennie that PhD in condensed matter will make you highly employable
Employed in?
If it would be industry , then a big no.
@SwapnilDas Both academia and industry.
12:55
@SwapnilDas take a look at this paper
https://arxiv.org/abs/1206.4276
Its the best example that I know of how condensed matter and high-energy physics (including gravity) are connected
Actually industry doesn't really care what PhD you have as long as it isn't completely unrrelated. As far as most companies are concerned the PhD just means you're bright and hard working, which is obviously good for them.
@JohnRennie I saw some papers. It is more of materials than fundamental physics :(
But when you're looking for post-docs you'll find far more openings in condensed matter than GR.
@SwapnilDas no, no, no :-)
Try reading Witten's papers on symmetry breaking and superconductivity and tell me it's all just materials :-)
Witten in CM!
6
Q: Seiberg-Witten theory and Superconductivity

wonderichThere seems to have some (deep) relation between Seiberg-Witten theory and superconductivity. e.g. this Witten paper. Q: Could someone introduce the relations between the twos both physically in terms of intuition? and mathematically in terms of formalism? How exactly is the relation?

12:59
@SolenodonParadoxus thanks for the paper. Is there a special name for their junction?
@SwapnilDas luckily for us, it is pretty legal to change the research subject :)
My advice will be - don't worry that you'll "get stuck" with condensed matter.
But the choice is ultimately yours and nobody should have to make it for you :)
I even don't like it that much.
Well you have your answer, then)
13:01
I like gravitational physics :)
Yes, but it's been stagnant for quite an amount of time
That's sad.
I'm willing to bet that the situation will change in 15 years though :)
@JohnRennie silly question. Do condensed matter theorist have to study organic chemistry?
@SolenodonParadoxus Golden words. I'll be 30 then ;)
You're 15 years old and you are choosing a PhD topic? :D
13:03
Nah :P I just get hooked with physics.
On my own right, I'll be 16 on Monday :)
@SolenodonParadoxus is Ads/CFT a research topic?
@SwapnilDas it is obviously
Yay!
Physics is so beautiful.
Is there a formula relating the refractive index and the speed of sound of a medium?
I don't think speed of sound and optical density of a medium are related. Moreover speed of sound in a given medium is a specified speed(at a given temperature) and not relative like RI.
@DanielSank I'd argue that one should write new projects in python 3 (except a few very rare cases), and should even consider porting existing ones. For the same reason you said: so that we don't end up with "most code being python 2" when they pull the plug;)
The python wall of superpowers (née wall of shame) shows that the vast majority of packages are available in python 3, and some scientific projects are pledging to abandon python 2 :)
also, hi
13:30
@AndrasDeak Good advice
13:52
@vzn You around?
14:39
I am reading "advice for a young investigator" by Cajal. It makes perfect sense to me, but I wonder how much of the advice applicable to physics science? (especially I would probably go into theoretical physics)
or rather, what especially he suggests fails in the field of physics?
15:27
@SwapnilDas No. There is organic condensed matter research e.g. in electrical properties of polymers, but that's a small part of a huge field.
vzn
vzn
15:56
@BernardMeurer hi
@Shing have that book, recommend it, think the advice is mostly generic and carries across fields, hes highly regarded in neurobiology and there is some crossover
@DavidZ was thinking, wanted to follow up on this. emotion aside, wondering if you have any ref for "how physics theory/ axioms might change" esp by a theorist/ expert/ authority. in particular could there be some reappraisal/ reconsideration of michelson/ morely & lorentz "ether wind/ contraction"/ preferred reference frame ideas... personally think tenev/ horstemeyer is promising/ applicable
morely morley
16:35
I don't believe I have anything to offer along those lines

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