Up to what temperature is petroleum stable? New insights from a 5200 free radical reactions model     

Florent Domin  Roda Bounaceur  Gerard Scacchi  Paul-Marie Marquaire  Daniel Dessort  Bernard Pradier  Olivier Brevart 《Organic Geochemistry》2002,33(12)

The discovery of crude oils and condensates at ever higher temperatures casts doubt on the validity of the usual geochemical modelling approach, that uses empirical reactions and rate constants. The solution used to account for such a high thermal stability is presently to adjust the rate parameters, but the physical meaning and scientific value of such a strategy can be questioned. We have developed a mechanistic model consisting of 5200 lumped free radical reactions to describe the thermal evolution of a mixture of 52 organic species meant to represent light petroleum. Rate constants used are those available in the literature or estimated using well established thermochemistry-reactivity correlations. Chemical structures included in the model are linear, branched and cyclic hydrocarbons, hydro- and alkyl-aromatics, PAHs, and three heteroatomic compounds. Reactions include cracking and alkylation chains and inhibiting and accelerating reactions from the various reactants. This model has been applied to several mixtures with various proportions of reaction inhibitors and accelerators, and to a composition representing a light mature oil. From the results obtained, we conclude that mature oils will be stable up to 240–260 °C, depending on their composition, and that the thermal cracking of oil to gas is not possible under reasonable basin conditions. The kinetics of petroleum cracking are thus much slower than generally recognized.  相似文献   

Thermal decomposition process in algaenan of Botryococcus braunii race L. Part 2: Molecular dynamics simulations using the ReaxFF reactive force field     

Elodie Salmon  Adri C.T. van Duin  François Lorant  Paul-Marie Marquaire  William A. Goddard 《Organic Geochemistry》2009,40(3):416-427

This paper reports ReaxFF MD simulation results on pyrolysis of a molecular model of the algaenan Botryococcus braunii race L biopolymer, specifically, ReaxFF predictions on the pyrolysis of prototypical chemical structures involving aliphatic chain esters and aldehydes. These preliminary computational experiments are then used to analyze the thermal cracking process within algaenan race L biopolymers. The simulations indicate that the thermal decomposition of the algaenan biopolymer is initiated by the cleavage of a C–O bond in the ester group, followed by the release of carbon dioxide. We also observe a significant, strongly temperature dependent, release of ethylene. This degradation mechanism leads to products similar to those observed in pyrolysis experiments, validating this computational approach.  相似文献   

Early maturation processes in coal. Part 1: Pyrolysis mass balance and structural evolution of coalified wood from the Morwell Brown Coal seam     

Elodie Salmon  Françoise Behar  François Lorant  Patrick G. Hatcher  Paul-Marie Marquaire 《Organic Geochemistry》2009,40(4):500-509

We have developed a theoretical approach for evaluating the maturation of kerogen-like material, involving molecular dynamic reactive modelling with a reactive force field to simulate thermal stress. Morwell Brown Coal was selected to study the thermal evolution of terrestrial organic matter (OM). To achieve this, a structural model is first constructed on the basis of literature models and analytical characterization of our samples using modern 1and 2D nuclear magnetic resonance (NMR) spectroscopy, Fourier transform infrared (FTIR) spectroscopy and elemental analysis. Then, artificial maturation of the coal is performed at low conversion in order to obtain quantitative and qualitative detailed evidence for the structural evolution of the kerogen upon maturation. The chemical changes include defunctionalization of carboxyl, carbonyl and methoxy functional groups, coupled with an increase in cross linking in the residual matured kerogen. Gaseous and liquid hydrocarbons, essentially CH₄, C₄H₈ and C₁₄₊ hydrocarbons, are generated in low amount, merely via cleavage of the lignin side chain.  相似文献   

Thermal decomposition processes in algaenan of Botryococcus braunii race L. Part 1: Experimental data and structural evolution     

Elodie Salmon  Françoise Behar  François Lorant  Patrick G. Hatcher  Pierre Metzger  Paul-Marie Marquaire 《Organic Geochemistry》2009,40(3):400-415

The thermal reactivity of organic matter in source rocks is usually kinetically represented by a set of parallel and independent first order reactions. The approach assumes that only defunctionalisation reactions take place upon thermal decomposition, regardless of the chemical nature of kerogen. We have developed a new method for evaluating maturation pathways for an important kerogen-forming geopolymer, algaenan from the alga Botryococcus braunii (B. braunii), involving molecular dynamic reactive modelling based on quantum mechanics to reproduce maturation. To achieve this, a structural model is first constructed on the basis of models from the literature and analytical characterization of our samples using modern 1D and 2D nuclear magnetic resonance spectroscopy (NMR), Fourier transform infrared spectroscopy (FTIR) and elemental analysis (EA). Then, thermal decomposition of the algaenan is performed at low conversion in order to describe the initial transformations analytically. In an additional step, the observed chemical changes are quantitatively and qualitatively compared to simulated maturation from the molecular models. From this simulated maturation detailed reaction schemes are extracted for primary cracking mechanisms.  相似文献   

Thermal evolution of n- and iso-alkanes in oils. Part 1: Pyrolysis model for a mixture of 78 alkanes (C₁-C₃₂) including 13,206 free radical reactions     

V. Burklé-Vitzthum  R. BounaceurP.-M. Marquaire  F. MontelL. Fusetti 《Organic Geochemistry》2011,42(5):439-450

A mechanistic model consisting of 13,206 lumped free radical reactions has been developed to describe the thermal evolution of a mixture of 78 alkanes: all n-alkanes from C₁ to C₃₂ and 46 branched alkane model compounds from C₄ to C₃₂. The mixture was meant to represent the major part of the saturated fraction of petroleum. The rate constants used are available from the literature. The lumping together procedure is described and the model validated on the basis of several experimental results from the literature and relating to pure alkanes. The model is also compared to the saturated fraction obtained from pyrolysis of Elgin oil at 372 °C for up to 1000 h. The cracking global activation energy of n-C₁₅ as well as iso-C₁₅ is close to 69 kcal/mol in the range 200-350 °C. The implications of the model for geological reservoirs will be discussed in a following paper.  相似文献   

Early maturation processes in coal. Part 2: Reactive dynamics simulations using the ReaxFF reactive force field on Morwell Brown coal structures     

Elodie Salmon  Adri C.T. van Duin  François Lorant  Paul-Marie Marquaire  William A. Goddard 《Organic Geochemistry》2009,40(12):1195-1209

This paper reports reactive dynamics (RD) simulations of a macro-model of Morwell Brown coal using the ReaxFF reactive force field. We find that these reactive MD simulations successfully reproduce thermal decomposition processes of defunctionalization, depolymerization and rearrangement of the residual structure observed in various experimental studies. For example, our simulations indicate that the decarboxylation and dehydroxylation of the lignin side chain of the Morwell model involves the formation of double bonds conjugated with the aromatic rings. The process of defunctionalization of the methoxy functions involving the formation of phenolic structures in the residue has been confirmed. We also observe that gaseous hydrocarbons are generated by cleavage of C–C bonds of the lignin side chain.The success in using ReaxFF RD to describe the molecular processes underlying the kinetics in pyrolysis of this model of coal plus the success of a similar previous study on the algaenan of Botryococcus braunii race L biopolymer model of kerogens suggests that such computation can be useful in providing molecular based kinetic models for other pyrolysis processes underlying the organic transformations in sedimentary materials.  相似文献