Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDoes divergent selection predict the evolution of mate preference and reproductive isolation in the tropical butterfly genus Melinaea (Nymphalidae: Ithomiini)?    Next AbstractMicroextraction of volatile organic compounds using the inside needle capillary adsorption trap (INCAT) device »

Orig Life Evol Biosph


Title:Abiotic formation of hydrocarbons and oxygenated compounds during thermal decomposition of iron oxalate
Author(s):McCollom TM; Simoneit BR;
Address:"Petroleum and Environmental Geochemistry Group, College of Oceanic and Atmospheric Sciences, Oregon State University, Corvallis 97331, USA. tmccollom@whoi.edu"
Journal Title:Orig Life Evol Biosph
Year:1999
Volume:29
Issue:2
Page Number:167 - 186
DOI: 10.1023/a:1006556315895
ISSN/ISBN:0169-6149 (Print) 0169-6149 (Linking)
Abstract:"The formation of organic compounds during the decomposition of iron oxalate dihydrate (IOD) was investigated as a possible analog for abiotic organic synthesis in geological systems. After heating at 330 degrees C for 2-4 days, IOD decomposed to a mixture of the minerals siderite and magnetite plus gas and non-volatile organic compounds. The organic products included an extremely large variety of compounds, making identification of individual reaction products difficult. However, the non-volatile products were dominated by several homologous series of alkylated cyclic compounds mostly containing a single aromatic ring, including alkylphenols, alkylbenzenes, alkyltetrahydronaphthols, and alkyltetrahydronaphthalenes. Traces of n-alkanols, n-alkanoic acids, n-alkanones, and n-alkanes were also identified. Carbon in the gas phase was predominantly CO2 (+CO?), with lesser amounts of light hydrocarbons to > C6 including all possible branched and normal isomers of the alkanes and alkenes. The organic products were apparently the result of two concurrent reaction processes: (1) condensation of the two-carbon units present in the initial oxalate moiety, and (2) Fischer-Tropsch-type synthesis from CO2 or CO generated during the experiment. Compounds produced by the former process may not be characteristic of synthesis from the single-carbon precursors which predominate in geologic systems, suggesting iron oxalate decomposition may not provide a particularly suitable analog for investigation of abiotic organic synthesis. When water was included in the reaction vessels, CO2 and traces of methane and light hydrocarbon gases were the only carbon products observed (other than siderite), suggesting that the presence of water allowed the system to proceed rapidly towards equilibrium and precluded the formation of metastable organic intermediates"
Keywords:Ferrosoferric Oxide Gas Chromatography-Mass Spectrometry Hot Temperature Hydrocarbons/*chemical synthesis/chemistry Iron Oxalates/*chemistry Oxides Oxygen NASA Discipline Exobiology Non-NASA Center;
Notes:"MedlineMcCollom, T M Simoneit, B R eng Research Support, U.S. Gov't, Non-P.H.S. Netherlands 1999/05/05 Orig Life Evol Biosph. 1999 Mar; 29(2):167-86. doi: 10.1023/a:1006556315895"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 18-11-2024