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Volumn 276, Issue 5311, 1997, Pages 390-392

Organic synthesis in experimental impact shocks

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE; CARBON DIOXIDE; HYDROGEN CYANIDE; METHANE; ORGANIC COMPOUND;

EID: 0030620488     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.276.5311.390     Document Type: Review
Times cited : (87)

References (33)
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    • note
    • 2. The gases other than water were obtained as premixed research-grade gases. This gas was added to the correct amount of distilled water in a 250-ml glass flask to achieve the final mixture. The sample flasks and the controls were placed within an oven held at 80°C, such that all the water was in vapor form.
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    • Paris, 11 to 15 February Columbia Univ. Press, New York
    • Typically, the beam contained ∼0.2 J in a pulse of ∼15 ns, repeated 10 times a second (6). A plasma formed when the laser beam was brought to a focus, as first reported by P. D. Maker, R. W. Terhune, C. M. Savage [in Proceedings of the 3rd International Conference on Quantum Electronics, Paris, 11 to 15 February 1963 (Columbia Univ. Press, New York, 1964), vol. 2, pp. 1559-1576]. See also Yu. P. Raizer, Sov. Phys. Usp. 8, 650 (1966); L. R. Radziemski, T. R. Loree, D. A. Cremers, N. M. Hoffman, Anal. Chem. 55, 1246 (1983); D. D. Davis, G. R. Smith, W. A. Guillory, Origins Life 10, 237 (1980). The spectral properties and optical emission of the laser-induced plasma have been characterized (6, 13, 23, 24). For gas-phase analysis, we used a 4-min exposure. The total energy deposited is sufficient to heat only about 15% of the gas to a freeze-out temperature of 2500 K. However, some experiments were conducted in which the exposure time was increased to 20 min to allow for maximal processing of the mixture and the production of a solid residue. The laser output was directly measured with a bolometric power meter. None of the gaseous species in the experiment caused significant absorption at the 1.06-μm laser line over the short pathlengths (1 cm) used. The efficiency with which this power was converted to plasma energy was determined by direct measurement of the total power deposited in the test chamber as described (24).
    • (1963) Proceedings of the 3rd International Conference on Quantum Electronics , vol.2 , pp. 1559-1576
    • Maker, P.D.1    Terhune, R.W.2    Savage, C.M.3
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    • 0001418637 scopus 로고
    • Typically, the beam contained ∼0.2 J in a pulse of ∼15 ns, repeated 10 times a second (6). A plasma formed when the laser beam was brought to a focus, as first reported by P. D. Maker, R. W. Terhune, C. M. Savage [in Proceedings of the 3rd International Conference on Quantum Electronics, Paris, 11 to 15 February 1963 (Columbia Univ. Press, New York, 1964), vol. 2, pp. 1559-1576]. See also Yu. P. Raizer, Sov. Phys. Usp. 8, 650 (1966); L. R. Radziemski, T. R. Loree, D. A. Cremers, N. M. Hoffman, Anal. Chem. 55, 1246 (1983); D. D. Davis, G. R. Smith, W. A. Guillory, Origins Life 10, 237 (1980). The spectral properties and optical emission of the laser-induced plasma have been characterized (6, 13, 23, 24). For gas-phase analysis, we used a 4-min exposure. The total energy deposited is sufficient to heat only about 15% of the gas to a freeze-out temperature of 2500 K. However, some experiments were conducted in which the exposure time was increased to 20 min to allow for maximal processing of the mixture and the production of a solid residue. The laser output was directly measured with a bolometric power meter. None of the gaseous species in the experiment caused significant absorption at the 1.06-μm laser line over the short pathlengths (1 cm) used. The efficiency with which this power was converted to plasma energy was determined by direct measurement of the total power deposited in the test chamber as described (24).
    • (1966) Sov. Phys. Usp. , vol.8 , pp. 650
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    • Typically, the beam contained ∼0.2 J in a pulse of ∼15 ns, repeated 10 times a second (6). A plasma formed when the laser beam was brought to a focus, as first reported by P. D. Maker, R. W. Terhune, C. M. Savage [in Proceedings of the 3rd International Conference on Quantum Electronics, Paris, 11 to 15 February 1963 (Columbia Univ. Press, New York, 1964), vol. 2, pp. 1559-1576]. See also Yu. P. Raizer, Sov. Phys. Usp. 8, 650 (1966); L. R. Radziemski, T. R. Loree, D. A. Cremers, N. M. Hoffman, Anal. Chem. 55, 1246 (1983); D. D. Davis, G. R. Smith, W. A. Guillory, Origins Life 10, 237 (1980). The spectral properties and optical emission of the laser-induced plasma have been characterized (6, 13, 23, 24). For gas-phase analysis, we used a 4-min exposure. The total energy deposited is sufficient to heat only about 15% of the gas to a freeze-out temperature of 2500 K. However, some experiments were conducted in which the exposure time was increased to 20 min to allow for maximal processing of the mixture and the production of a solid residue. The laser output was directly measured with a bolometric power meter. None of the gaseous species in the experiment caused significant absorption at the 1.06-μm laser line over the short pathlengths (1 cm) used. The efficiency with which this power was converted to plasma energy was determined by direct measurement of the total power deposited in the test chamber as described (24).
    • (1983) Anal. Chem. , vol.55 , pp. 1246
    • Radziemski, L.R.1    Loree, T.R.2    Cremers, D.A.3    Hoffman, N.M.4
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    • 0019056030 scopus 로고
    • Typically, the beam contained ∼0.2 J in a pulse of ∼15 ns, repeated 10 times a second (6). A plasma formed when the laser beam was brought to a focus, as first reported by P. D. Maker, R. W. Terhune, C. M. Savage [in Proceedings of the 3rd International Conference on Quantum Electronics, Paris, 11 to 15 February 1963 (Columbia Univ. Press, New York, 1964), vol. 2, pp. 1559-1576]. See also Yu. P. Raizer, Sov. Phys. Usp. 8, 650 (1966); L. R. Radziemski, T. R. Loree, D. A. Cremers, N. M. Hoffman, Anal. Chem. 55, 1246 (1983); D. D. Davis, G. R. Smith, W. A. Guillory, Origins Life 10, 237 (1980). The spectral properties and optical emission of the laser-induced plasma have been characterized (6, 13, 23, 24). For gas-phase analysis, we used a 4-min exposure. The total energy deposited is sufficient to heat only about 15% of the gas to a freeze-out temperature of 2500 K. However, some experiments were conducted in which the exposure time was increased to 20 min to allow for maximal processing of the mixture and the production of a solid residue. The laser output was directly measured with a bolometric power meter. None of the gaseous species in the experiment caused significant absorption at the 1.06-μm laser line over the short pathlengths (1 cm) used. The efficiency with which this power was converted to plasma energy was determined by direct measurement of the total power deposited in the test chamber as described (24).
    • (1980) Origins Life , vol.10 , pp. 237
    • Davis, D.D.1    Smith, G.R.2    Guillory, W.A.3
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    • note
    • -3 at 4.0 μS after ignition. The electron temperature dropped from 17,000 to 12,000 K over this same interval.
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    • note
    • Spectral comparison of the temperature and pressure history of the laser plasma and natural lightning (12, 13) indicated that at temperatures near the freeze-out (2000 to 3000 K) the trajectories on a pressure-temperature diagram are similar.
  • 20
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    • note
    • 2 mixtures were analyzed with a Varian 9600 gas chromatograph. Taking into account the variation in the amount of water entered into the sample and variations in the laser beam energy and flask transmission, we conservatively estimated that our values are accurate to a factor of 2. Improved identification could be achieved if the parent gases are removed by cryogenic cooling. Samples and controls were kept shielded from sunlight and room light. No measurable production of organics was found in the controls.
  • 21
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    • note
    • The solid residue was analyzed by solution in boiling dichloromethane and in methanol. No organic material was detected at a level of 1 ppm in the dichloromethane. The methanol solution, examined with a Fourier Transform Infrared Spectrometer (IBM model 32), indicated the presence of soluble organic matter. Infrared absorption bands were identified at 2922, 2855, and 1450 wavenumbers, indicating the presence of aliphatic hydrocarbons; at 1516 wave-numbers, indicating a small amount of aliphatic amine; at 1636 wavenumbers, indicating an amide group; and at 1117 wavenumbers, indicating the possible presence of alcohol groups. We could not accurately determine the yield of the solid residue because of the long exposure time required to produce this material and the resulting reprocessing of products. However, based on the exposure time (20 min) and product amount (determined to be about 0.01 mg on the basis of concentrations in solution), we can estimate its yield at about 1% of the yield of the major hydrocarbons. An x-ray fluorescence spectrum of the solid residue showed a strong sulfur line, indicating incorporation at the few percent level in the solid residue.
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    • note
    • 6, and 0.1 to 1% HCN. Our results correspond to similar yields for the UV production, ≃1 to 10% of the total shock production is due to UV.
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    • J. B. Pollack, Y. L. Yung, Annu. Rev. Earth Planet. Sci. 8 425 (1980); H. D. Holland, The Chemical Evolution of the Atmosphere and Oceans (Princeton Univ Press, Princeton, NJ, 1984).
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    • 2 has been removed to account for oxides in the rock fraction of the cometary material, as in D. Simonelli, J. B. Pollack, C. P. McKay, R. T. Reynolds, and A. L. Summers [Icarus 62, 1 (1989)].
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    • note
    • This research was supported by subventions from the NASA Exobiology Program. We thank M. Carter of Carter Analytical Laboratories for performing the GC-MS analysis and for helpful discussions. GC analysis was performed by D. Kojiro, F. Church, and R. Quinn.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.