Superconductor coil experiment video Updated 2025-07-16
TODO!!! Even this is hard to find! A clean and minimal one! Why! All we can find are shittly levitating YBCO samples in liquid nitrogen! Maybe because liquid helium is expensive?
Video 1.
First 10T Tape Coil by Mark Benz
. Source. Dr. Mark Benz describes the first commercially sold superconducting magnet made by him and colleagues in 1965. The 10 Tesla magnet was made at GE Schenectady and they sold magnets to research facilities world wide before the team formed Intermagnetics General. IGC and Carl Rosner went on to pioneer MRI technology.
Video 1.
Superconductor, 4-probe measurement by Frederiksen Scientific A/S (2015)
Source. OK experiment, illustrates the educational kit they sell. No temperature control, just dumps liquid nitrogen into conductor and watches it drop. But not too bad either. The kit sale link is broken (obviously, enterprise stuff), but there are no archives unfortunately. But it must be some High-temperature superconductor
Shooter game Updated 2025-07-16
Ciro's Edict #5 / Not work Updated 2025-07-16
I read Human Compatible by Stuart J. Russell (2019). Some AI safety people were actually giving out free copies after a talk, can you believe it! Good book.
Superfluidity Updated 2025-07-16
Video 1.
Alfred Leitner - Liquid Helium II the Superfluid by Alfred Leitner (1963)
Source. Original source: www.alfredleitner.com.
Video 2.
Ben Miller experiments with superfluid helium by BBC (2011)
Source. Just quickly shows the superfluid helium climbing out o the cup, no detailed setup. With professor Robert Taylor from the University of Oxford.
Super-resolution microscopy Updated 2025-07-16
Super-resolution means resolution beyond the diffraction limit.
First you shine a lot of light which saturates most fluorophores, leaving very few active.
They you can observe fluorophores firing one by one. Their exact position is a bit stochastic and beyond the diffraction limit, but so long as there aren't to many in close proximity, you can wait for it to fire a bunch of times, and the center of the Gaussian is the actual location.
From this we see that super-resolution microscopy is basically a space-time tradeoff: the more time we wait, the better spacial resolution we get. But we can't do it if things are moving too fast in the sample.
Tradeoff with cryoEM: you get to see things moving in live cell. Electron microscopy fully kills cells, so you have no chance of seeing anything that moves ever.
Caveats:
  • initial illumination to saturate most fluorophores I think can still kill cells, things get harder the less light you put in. So it's not like you don't kill things at all necessarily, you just get a chance not to
  • the presence fluorophore disturbs the system slightly, and is not at the same Exact location of the protein of interest
Maser Updated 2025-07-16
Video 1.
Principles of the Optical Maser by Bell Labs
. Source. Date: 1963.
Netflix Updated 2025-07-16
Why are there two sexes? Updated 2025-07-16
It is not obvious why there have to be two sexes.
Sex itself is obvious: by mixing genes we increase variability.
But having two sexes rather than just being able to reproduce with anyone reduces the possible mating pool by half!
Go (programming language) Updated 2025-07-16
Likely a good replacement for Python. If the ecosystem gets there, Ciro Santilli would gladly use it more.

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