lsparrish
Joined 16 years ago
Joined 16 years ago
You can draw fibers, use cantilevers, exploit the wavelength properties of laser light, electromagnetically control the path of ionized materials in a vacuum, use piezoelectric actuators that convert current to angstrom level movements, and so on. Not to mention the many approaches to coating a surface with a very thin layer: vacuum deposition, spin coating, electroplating, etc.
That is the textbook answer, however these bonds are only "irreversible" as a matter of biochemistry. You can actually break any chemical bond by increasing the temperature enough. The problem for our purposes is that this means destroying the structure.
> There is zero hope that this provides a solution to cryopreservation except in the slice it up and look at it under the microscope sense.
The trick to reversing the bond without damaging the structure would be in delivering high enough amounts of energy with high enough precision to have only the intended effects. This may or may not be physically possible. However, to rule out the possibility completely, we would need to consider a wide variety of physical interactions that are well outside the range of biology and wet-solvent chemistry, in addition to the full spectra of potential biomimetic and biological approaches.
I might have misunderstood this bit (in which case, oops). I see way too many people making the assumption that cryonics is somehow primarily profit motivated. Taking money out of the cryonics trust to "buy drinks" would potentially cost the lives of patients, as the organization must remain stable in addition to the revival being achievable to begin with. The incentive is towards long term savings.
> So, how about my watch, asks one of the people that handed over his watch and his money. "Oh, that's the hard part, I haven't really studied that yet, come back in a few 100 years and I might have your watch again. But I'm getting better at smashing watches, that's for sure."
This analogy doesn't make much sense to me. Cryonics is about trying to prevent something that will inevitably be smashed from being smashed as badly. Saying cryonics is about smashing things is like saying seat belts are about cars crashing into each other.
HOV is using extremely high concentrations of solutes to reduce the freezing point (a colligative property). That is the only way to vitrify something big like the brain. At least, until some super material is invented that lets us pull out lots of heat really fast. The trouble is that it is toxic to cells to be exposed for very long. With rabbit kidneys and small slices of brain tissue, the exposure time at warm temperatures can be very brief. So with current cryonics we can only make a morphological argument for information theoretic preservation.
With better materials that enable faster cooling, prevent the toxicity mechanisms of the cryoprotectant, and/or block ice formation non-colligatively (certain polymers do this), it is theoretically possible that we could get to a point where the cells are still viable. In that event, it would be like placing the brain in an "off state". You wouldn't be able to resume it again without a body to implant it in, but that's more likely to be on the 200-year radar than nanorepair, so the chances would be improved quite a bit. Also, I suspect more people would sign up for a process that does not involve "killing" their brain cells.
With really thin sails (0.78 g/m^2) they don't even need to orbit, as they can use light pressure to compensate for gravity (what Robert Forward termed a 'statite'). The light they reflect hits other sails on the other side, but this isn't a problem if they are distributed uniformly.