Abstract: Method and apparatus for determining the relative content of a first rock species and of a second rock species in a rock sample extracted from a wellbore. The method comprises adding a reactant to the rock sample, measuring a first information (PT1) relative to a first amount of compound produced at a first instant (T1) and a second information (PT2) relative to a second amount of compound produced at a second instant (T2). The method also comprises calculating the relative content of the first species in the rock sample from the first information (PT1) and calculating the relative content of the second species in the rock sample from the second information PT2). The method comprises determining a corrected amount (Cv) of compound generated by the reaction of the second species with the reactant at the first instant (T1), and calculating the relative content of the first species in the rock sample and the relative content of the second species in the rock sample based on the corrected amount (Cv).

Abstract: Method and apparatus for determining the relative content of a first rock species and of a second rock species in a rock sample extracted from a wellbore. The method comprises adding a reactant to the rock sample, measuring a first information (PT1) relative to a first amount of compound produced at a first instant (T1) and a second information (PT2) relative to a second amount of compound produced at a second instant (T2). The method also comprises calculating the relative content of the first species in the rock sample from the first information (PT1) and calculating the relative content of the second species in the rock sample from the second information PT2). The method comprises determining a corrected amount (Cv) of compound generated by the reaction of the second species with the reactant at the first instant (T1), and calculating the relative content of the first species in the rock sample and the relative content of the second species in the rock sample based on the corrected amount (Cv).

Abstract: The method comprises placing a sample of rock on a mold surface (90), forming a solid plug (134) containing the rock sample embedded in a hardened resin matrix. The method further comprises pouring a UV polymerizable liquid resin on the sample of rock to embed the sample of rock in liquid resin and passing the rock sample embedded in the UV polymerizable liquid resin in a polymerization device (66) comprising a UV source (92) to harden the liquid resin and form the plug (134).

Abstract: The device comprises an apparatus (75) including a sampling sleeve (80) fixed around a sampling opening (53) provided in the duct (25) and a sampling head (81), introduced in the sampling sleeve (80) to be submerged in the circulating fluid, the sampling head (81) defining at least one fluid sampling opening (93). The device comprises a filtration member (85), having a filtration wall (99) arranged in the vicinity of the sampling opening (93) to filter the fluid introduced through the sampling opening (93), and a mobile member (87) rotatably mounted around an axis (C-C?) of rotation relative to the sampling head (81) to ensure at least partial cleaning of the filtration wall (99). The sampling apparatus (75) comprise a sealing assembly (87A) able to seal the sampling sleeve (80) around the sampling head (81) when the sampling head (81) is inserted in the sampling sleeve (80).

Abstract: The method includes extraction of gases contained in a mud, in order to obtain a gas stream of extracted gases containing hydrocarbons to be analyzed and at least one parasitic compound. The method includes transporting the gas stream through a transport line (54) and passing it through a separation column (121) in order to separate the hydrocarbons to be analyzed according to their elution times in the separation column (121). The parasitic compound is likely to have an elution time in the separation column (121) between the elution time for the first hydrocarbon to be analyzed and the elution time of the final hydrocarbon to be analyzed. The method includes passing the gas stream over a surface (141) for chemical and/or physical interaction with the parasitic compound in order to selectively retain the or each parasitic compound without retaining the hydrocarbons to be analyzed.

Abstract: The method includes extraction of gases contained in a mud, in order to obtain a gas stream of extracted gases containing hydrocarbons to be analyzed and at least one parasitic compound. The method includes transporting the gas stream through a transport line (54) and passing it through a separation column (121) in order to separate the hydrocarbons to be analyzed according to their elution times in the separation column (121). The parasitic compound is likely to have an elution time in the separation column (121) between the elution time for the first hydrocarbon to be analyzed and the elution time of the final hydrocarbon to be analyzed. The method includes passing the gas stream over a surface (141) for chemical and/or physical interaction with the parasitic compound in order to selectively retain the or each parasitic compound without retaining the hydrocarbons to be analyzed.

Abstract: Use of a nebulizer add-gas to reduce metal deposition on the sampling orifices of an inductively coupled plasma mass spectrometer (“ICP-MS”) is disclosed. Specifically, dilute mixtures of Sulfur Hexafluoride (SF6) in an inert gas have been used to reduce transition metal deposition on the sampling orifices of an ICP-MS, thereby greatly enhancing the stability of the ICP-MS sensitivity over time without corroding the internal parts and/or chemically attacking the cones of the ICP-MS.

Abstract: Use of a nebulizer add-gas to reduce metal deposition on the sampling orifices of an inductively coupled plasma mass spectrometer (“ICP-MS”) is disclosed. Specifically, dilute mixtures of Sulfur Hexafluoride (SF6) in an inert gas have been used to reduce transition metal deposition on the sampling orifices of an ICP-MS, thereby greatly enhancing the stability of the ICP-MS sensitivity over time without corroding the internal parts and/or chemically attacking the cones of the ICP-MS.