Method for quantifying the pyritic sulfur and the organic sulfur of a rock sample

Patent metadata

Field	Value
Publication number	US-10895567-B2
Application number	US-201816127785-A
Country	US
Kind code	B2
Filing date	Sep 11, 2018
Priority date	Sep 12, 2017
Publication date	Jan 19, 2021
Grant date	Jan 19, 2021

Abstract

A method which distinctly characterizes and quantifies the pyritic sulfur and the organic sulfur of a sedimentary rock sample. A rock sample is subjected to a heating sequence in an inert atmosphere which produces effluents resulting which are continuously oxidized. SO2 is continuously measured, and a pyrolysis sulfur content and a pyrolysis pyritic sulfur content are deduced therefrom. The residue from heating in an inert atmosphere is then heated in an oxidizing atmosphere. Released SO2 is continuously measured and at least an oxidation sulfur content is deduced therefrom. The pyritic sulfur content is determined from pyrolysis, a weighting function, a second parameter representing the impact of the mineral matrix and a third parameter representing the impact of the organic matrix.

First claim

The invention claimed is:

1. A method for quantifying pyritic sulfur in a sedimentary rock sample, comprising:
A. heating the sample in an inert atmosphere, between a first temperature ranging between 100° C. and 320° C. and a second temperature ranging between 600° C. and 700° C., to produce effluents by following a first temperature gradient ranging between 1° C./min and 30° C./min;
B. continuously oxidizing at least part of the effluents obtained from heating the sample in an inert atmosphere and continuously measuring a first amount of SO 2 released as a function of time of the heating in an inert atmosphere, and determining at least a pyrolysis sulfur content from a area under a curve of the measured first amount of SO 2 released as a function of time and a pyrolysis pyritic sulfur content S Pyrol Pyrit from a area under a last peak of the curve of the measured first amount of SO 2 released as a function of time;
C. heating in an oxidizing atmosphere a residue of the sample resulting from the heating in the inert atmosphere between a third temperature ranging between 280° C. and 320° C. and a fourth temperature at least equal to 800° C., by following a second temperature gradient ranging between 1° C./min and 30° C./min;
D. continuously measuring a second amount of SO 2 released as a function of time of the heating in the oxidizing atmosphere and determining at least an oxidation sulfur content from a area under a curve of the measured second amount of SO 2 released as a function of time and determining at least a total sulfur content S Total by a sum of the pyrolysis sulfur content and the oxidation sulfur content; and

wherein at least a pyritic sulfur content S Pyrit of the sample is determined from a formula:
S Pyrit =p (α,α,γ)· S Pyrol Pyrit , wherein

p(α, β, γ) is a weighting function depending on a parameter α which represents a proportion of the pyrolysis pyritic sulfur relative to the total sulfur, parameter β which represents an effect of a mineral matrix of the sedimentary rock sample on the proportion, parameter γ which represents an effect of organic matrix of the sedimentary rock sample on the proportion with values of the parameters being predetermined.

2. A method as claimed in claim 1 , wherein the weighting function p(α, β, γ) is written as:

p
⁡

(

α
,
β
,
γ

)

=

(

1
+
β
+
γ

)

α

3. A method as claimed in claim 1 , wherein the sample is reservoir rock and the first temperature ranges between 100° C. and 200° C.

4. A method as claimed in claim 1 , wherein the sample is mother rock and the first temperature ranges between 280° C. and 320° C.

5. A method as claimed in claim 1 , wherein parameter α ranges between 0.40 and 0.46.

6. A method as claimed in claim 5 , wherein α is 0.43.

7. A method as claimed in claim 1 , wherein the rock sample is clay and parameter β ranges between 0.04 and 0.7.

8. A method as claimed in claim 7 , wherein β is 0.38.

9. A method as claimed in claim 1 , wherein the rock sample is marl and parameter β ranges between 0.7 and 0.9.

10. A method as claimed in claim 9 , wherein β is 0.78.

11. A method as claimed in claim 1 , wherein the rock sample is limestone and parameter β ranges between 0.85 and 0.97.

12. A method as claimed in claim 11 , wherein β is 0.9.

13. A method as claimed in claim 1 , wherein the rock sample contains organic matter of at least one of lacustrine and marine origin, and a value of parameter γ is 0.

14. A method as claimed in claim 1 , wherein the rock sample contains an organic matter of terrestrial origin and parameter γ ranges between 0.23 and 0.29.

15. A method as claimed in claim 14 , wherein γ is 0.26.

16. A method as claimed in claim 1 , wherein the fourth temperature ranges between 800° C. and 900° C., and an organic sulfur content S Org is determined according to a formula as follows:
S Org =S Total −S Pyrit .

17. A method as claimed in claim 1 , wherein the fourth temperature is greater than 1150° C. and less than 1250° C. in step C, and a sulfate sulfur content S Oxy Sulfa is additionally determined from a area under a last peak of the curve of the measured second amount of SO 2 released as a function of time in step D, and organic sulfur content is determined with a formula:
S Org =S Total −S Pyrit −S Oxy Sulfa , wherein, S Pyrit is pyritic sulfur content and S Total is a total amount of sulfur that is present.

18. A method as claimed in claim 1 , wherein at least one of the pyrolysis sulfur content and the pyrolysis pyritic sulfur content is determined from the first amount of SO 2 and from a pyrolysis sulfur calibration coefficient established on a reference sample whose sulfur content is known, wherein the reference sample is subjected at least to step A) and B) and the pyrolysis sulfur calibration coefficient is determined from an area under a curve of a measured amount of SO 2 released by the reference sample as a function of time during step A) and B).

19. A method as claimed in claim 18 , wherein the reference sample is native sulfur.

20. A method as claimed in claim 1 , wherein the oxidation sulfur content is determined from the second amount of SO 2 and from an oxidation sulfur calibration coefficient established from a reference sample whose sulfur content is known, wherein the reference sample is subjected at least to step C) and D) and the oxidation sulfur calibration coefficient is determined from an area under a curve of a measured amount of SO 2 released by the reference sample as a function of time during steps C) and D).

21. A method as claimed in claim 20 , wherein the reference sample is coal.

22. A method as claimed in claim 1 , further comprising:
measuring amounts of hydrocarbon products of CO and CO 2 contained in effluents that result from the heating of the sample in an inert atmosphere; and
measuring amounts of CO and CO 2 contained in effluents resulting from the heating in an oxidizing atmosphere.

Assignees

• Ifp Energies Now

Inventors

• Aboussou Anabel
• Lamoureux-Var Violaine
• Pillot Daniel
• Kowalewski Isabelle
• Doligez Brigitte
• Garcia Bruno
• Wagner Thomas
• Buckman James Oliver
• Marz Christian

Classifications

• G01N33/24 Primary

  Earth materials (G01N33/42 takes precedence) · CPC title

• G01N31/005 Primary

  investigating the presence of an element by oxidation (G01N31/12 takes precedence) · CPC title

• G01N25/00

  Investigating or analyzing materials by the use of thermal means (G01N3/00 - G01N23/00 take precedence) · CPC title

• Y10T436/186

  Sulfur dioxide · CPC title

• G01N31/12

  using combustion (G01N25/20 takes precedence) · CPC title