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- From: merkle@parc.xerox.com (Ralph Merkle)
- Newsgroups: sci.nanotech
- Subject: Re: Some questions re "Nanosystems".
- Message-ID: <Dec.17.20.24.12.1992.25394@planchet.rutgers.edu>
- Date: 18 Dec 92 01:24:13 GMT
- Sender: nanotech@planchet.rutgers.edu
- Lines: 93
- Approved: nanotech@aramis.rutgers.edu
-
- > Topic 6: Nanosystems - New Drexler Book - Critique
- > By: Hudson Hayes Luce (hluce) on Sun, Nov 15, '92
-
-
- > For starters, let's look at p259, figs. 9.2a-e. Drexler terms these
- > structures
- > "diamondoid" and ascribes the properties of diamond to them. Diamond
- > is made up of carbon atoms covalently bonded to each other, and except
- > for the surface, all bonds are single bonds. All of the three-atom C-C-C bond
- > angles are 109.5 degrees, and all of the C-C-C-C bond dihedral angles are
- > + or - 120 degrees. This conformation minimizes strain energy. Moreover,
- > all of the rings in the structure are six-membered.
- >
- > However, in structure 9.2c, there are fused 3- and 4-membered rings, which
- > have bond angles of 60 degrees and 90 degrees, respectively, and whose
- > C-C-C-C dihedral angles, in some cases, are 0 degrees. This structure is
- > highly strained due to bond angle deformation and non-bonded steric
- > interactions. Compound 9.2c can thus be assumed to be highly unstable
- > at room temperatures, and is probably subject to thermodynamically-
- > driven rearrangement.
-
- To quote from "Molecular Mechanics," by Burkert and Allinger, ACS Monograph 177,
- page 117, "There are a substantial number of relatively simple, cyclopropane-
- containing molecules with known structures, or known heats of formation,
- or sometimes both. We exclude from consideration here a number of relatively
- large molecules containing a cyclopropane ring (in steroids, for example),
- for which crystallographic structures are available. These are not really
- suitable for parameterization of the cyclopropane part of a molecule, because
- there are too many other kinds of interactions present to complicate matters.
- The compounds examined (174) are shown below."
-
- There follows illustrations of 13 compounds which contain 3-member rings.
- Note that cyclopropane has 3 carbon atoms located at the corners of a triangle.
-
- The hexagonal form of carbon, which involves torsional angles of 0 degrees,
- exists in nature. To quote from "Modified Phases of Diamond Formed under
- Shock Compression and Rapid Quenching" by Hisako Hirai and Ken-Ichi Kondo,
- Science Vol. 253, page 772, August 16 1991: "Crystalline forms of pure
- carbon, such as diamond, lonsdaleite (hexagonal diamond), graphite, and
- carbynes have long been recognized. Diamond and hexagonal diamond have
- been synthesized by both static and dynamic high-pressure techniques."
-
- > On p265 Drexler states "acquiring and processing molecules from solution.."
- > in reference to a possible use of nanosystems, but on p5 he states that "The
- > operating environment assumed for the nanomechanical and mechano-
- > synthetic systems discussed in Part II is high vacuum"
- >
- > Describe a high-vacuum/solvent interface.
-
- This is illustrated on page 374, figure 13.1. There is a diamondoid wall
- between the liquid external environment and the high-vacuum internal
- environment. Figure 13.4 illustrates a multi-staged cascade which will
- produce an output with a contaminant fraction of less than 10^-15.
-
-
- > On p 196 it is stated, "In solution-phase chemistry, when molecular
- > potential
- > energy is transformed into mechanical energy, this promptly appears as heat
- > Reactions that reduce potential energy are accordingly termed exothermic,
- > those that increase it, endothermic. In mechanochemical systems, however,
- > potential energy released by a reaction can often be stored elsewhere in the
- > mechanical system, either as potential energy or as kinetic energy in the
- > form
- > of orderly motion"
- >
- > Potential energy can be transformed into kinetic energy. True.
- > Kinetic energy can be stored in the form of orderly motion. True.
- >
- > Kinetic energy can also be dissipated as heat, as random vibrational,
- > rotationl, or translational motion.
- >
- > Analyse Drexler's statement in light of the 2nd Law of Thermodynamics. If
- > this
- > statement is true, perpetual motion is possible.
-
- The second law is safe, and Drexler's statement in no way implies that
- violation of the second law is feasible. For a specific example of a
- mechanosynthetic process that converts chemical energy into energy elsewhere
- in the system, consider the analysis on page 223 (figure 8.6) of the
- cleavage of a C-C bond. Figure 8.7 illustrates the energies involved.
- The reaction is reversible, so mechanical energy can be converted either to
- or from chemical energy. The exact efficiency of this conversion will vary
- depending on the specific design.
-
- If we broaden the definition of "mechanochemical" to include biological
- muscles (which is reasonable in this case, as the underlieing principles
- governing energy conversion and dissipation in biological muscles are the
- same as the principles involved in systems that comply with the more
- specific definition of "mechanochemical" adopted by Drexler for "Nanosystems"),
- then Drexler's statement also applies to a person lifting a weight. Some
- fraction of the chemical potential energy that is released in the muscles
- is used to lift the weight, thus converting chemical energy into a mechanical
- form. Lifting weights does not violate the second law of thermodynamics.
-