Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G31/00—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for
  • C10G31/06—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for by heating, cooling, or pressure treatment
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
  • C10G29/20—Organic compounds not containing metal atoms
  • C10G29/205—Organic compounds not containing metal atoms by reaction with hydrocarbons added to the hydrocarbon oil
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G7/00—Distillation of hydrocarbon oils
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G7/00—Distillation of hydrocarbon oils
  • C10G7/06—Vacuum distillation
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
  • C23C16/04—Coating on selected surface areas, e.g. using masks
  • C23C16/045—Coating cavities or hollow spaces, e.g. interior of tubes; Infiltration of porous substrates
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
  • C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
  • C23C16/26—Deposition of carbon only
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/10—Feedstock materials
  • C10G2300/1037—Hydrocarbon fractions
  • C10G2300/1062—Lubricating oils
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/201—Impurities
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
  • Y02C20/00—Capture or disposal of greenhouse gases
  • Y02C20/20—Capture or disposal of greenhouse gases of methane

Definitions

• the present invention relates to the field of oils loaded with polycyclic aromatic hydrocarbons and their treatment.
• the classic scheme of a densification facility includes:
• the gas leaving the pyrocarbon densification reactor contains polycyclic aromatic hydrocarbons (PAHs).
• PAHs polycyclic aromatic hydrocarbons
• Gas treatment is essential to protect equipment from clogging phenomena caused by the presence of PAHs.
• Industrial installations include such gas treatments.
• Many means are used to stop PAHs (filtration, condensation, washing).
• the preferred method consists in washing the gas with an oil which has a high capacity for solubilizing PAHs, including under vacuum.
• patent applications WO 03/047725 and WO 2015/132527 describe such methods using aromatic mineral oils alone or as a mixture. with naphthenic mineral oil. Indeed these oils are the most effective for this type of treatment.
• the gas is thus treated by washing with cold oil before being pumped and upgraded. Therefore, the management of the washing fluid is of importance in the operation of the installations.
• Periodic oil renewal is a recurring cost that weighs on the cost of production.
• PAHs are CMR products which result in the loaded oil being considered as hazardous waste.
• such a process for treating these oils is not described in the prior art. Now, the inventors have noticed that it is possible to carry out such a treatment so as to be able to reuse the treated oils.
• the present invention therefore relates to a process for treating an aromatic mineral oil or a mixture of aromatic mineral oil and naphthenic mineral oil, said oil or said mixture of oils being loaded with polycyclic aromatic hydrocarbons (PAHs), advantageously containing at most 30% by volume of polycyclic aromatic hydrocarbons, characterized in that it comprises the following steps: a- optional elimination of polycyclic aromatic hydrocarbons having a molecular mass greater than or equal to 200 from aromatic mineral oil or mixture of aromatic mineral oil and naphthenic mineral oil loaded with polycyclic aromatic hydrocarbons; b- extraction under a pressure below atmospheric pressure of polycyclic aromatic hydrocarbons having a molecular mass of less than 200 dissolved in the oil or the mixture of oils obtained in step (a) c- recovery of the oil or of the mixture of oils depleted in polycyclic aromatic hydrocarbons.
• PAHs polycyclic aromatic hydrocarbons
• aromatic mineral oil or the mixture of aromatic mineral oil and naphthenic mineral oil are as described in patent applications WO 03/047725 and WO 2015/132527.
• the mixture of oils comprises at least 20% by volume of aromatic mineral oil relative to the total volume of the mixture, advantageously at least 30% by volume of aromatic mineral oil.
• the naphthenic mineral oil content depends on the viscosity to be achieved in the mixture.
• the mixture of oils can comprise at most 80% by volume of naphthenic mineral oil relative to the total volume of the mixture, in particular at most 70% by volume of naphthenic mineral oil.
• the mixture of oils comprises at least 10% by volume of naphthenic mineral oil relative to the total volume of the mixture, in particular at least 14% by volume of naphthenic mineral oil, more particularly at least 20% by volume of naphthenic mineral oil.
• the mixture of oils has a viscosity less than or equal to 150 mm 2 / s at 0 ° C. when the mixture does not contain PAH.
• the measurement of the kinematic viscosity of an oil according to the invention is carried out according to the ASTM D445 standard dated 2013 with an Ubbelhode viscometer with capillaries with a diameter of 0.88 mm. The viscosities are measured at 5 and 10 ° C and the viscosity at 0 ° C is obtained by linear extrapolation. Indeed, the measurement at 0 ° C is not directly achievable due to the condensation formed due to the large temperature difference between the room and the analysis system. The constant of the viscometer is measured with undecane.
• the aromatic mineral oil of the process according to the present invention is as described in patent application WO 03/047725.
• aromatic mineral oil has a low vapor pressure, preferably less than 1 Pa at 0 ° C.
• the aromatic mineral oil when it does not contain PAH, has a viscosity less than or equal to 75 mm 2 / s at 0 ° C, more particularly less than or equal to 73 mm 2 / s at 0 ° C. The viscosity is measured as indicated above for the mixture of oils.
• the aromatic mineral oil is an oil based on xylenes. It may thus be the synthetic oil marketed under the name “Jaritherm AX 320” by the French company Arkema and consisting of 85% by weight of mono-xylyxylene and 15% by weight of di-xylyxylene. This oil has a viscosity of 73 mm 2 / s at 0 ° C and a vapor pressure at 0 ° C less than 1 Pa. It can also be the aromatic mineral oil based on xylene marketed by the company TOTAL.
• LUBRICANTS under the name “Jaritherm BT06” and consisting of a mixture of dibenzyltoluene (20 to 30% by weight) and benzyltoluene (70 to 80% by weight) or of aromatic mineral oil based on xylene marketed by the company TOTAL LUBRIFIANTS under the name “Jaritherm DBT” and consisting of a mixture of isomers of dibenzyltoluene or alternatively of the aromatic mineral oil AZOLLA NET HC marketed by the company TOTAL LUBRIFIANTS.
• the naphthenic mineral oil of the process according to the invention can be a refined hydrodesulfurized naphthenic light distillate. Its paraffinic oil content is advantageously less than 50%. As for aromatic mineral oil, naphthenic mineral oil advantageously exhibits a low vapor pressure, preferably less than 1Pa at 0 ° C. Advantageously naphthenic mineral oil when it is not contains no PAH has a viscosity less than or equal to 75 mm 2 / s at 0 ° C, more preferably less than or equal to 70 mm 2 / s at 0 ° C, in particular less than or equal to 60 mm 2 / s at 0 ° C. The viscosity is measured as indicated above for the mixture of oils.
• the naphthenic mineral oil according to the present invention remains liquid at a temperature 3200 ° C, advantageously 3210 ° C, more advantageously 3240 ° C, even more advantageously 3250 ° C.
• it may be the naphthenic mineral oil marketed by the company TOTAL LUBRIFIANTS under the name “ISOVOLTINE II”. Naphthenic mineral oil should not be confused with naphthenic solvents.
• PAHs Polycyclic aromatic hydrocarbons
• naphthalene pyrene, phenanthrene, anthracene, acenaphthylene, acenaphthene and their mixtures, more particularly naphthalene, phenanthrene, acenaphthene and their mixtures.
• a list of PAHs is for example given in the table below.
• the polycyclic aromatic hydrocarbons are chosen from the list indicated in Table 1 and their mixtures, including acenaphthene, biphenyl, dibenzyltoluene and their mixtures.
• the PAHs are chosen from acenaphthene, acenaphthylene, biphenyl, dibenzyltoluene, naphthalene, fluorene, phenanthrene and their mixtures.
• the PAHs can be heavy PAHs (molecular weight greater than or equal to 200) or medium or light PAHs (molecular weight lower than 200), advantageously they are medium or light PAHs.
• PAHs are by-products of the chemical vapor deposition or infiltration reaction for the formation of pyrolytic carbon deposition on substrates or for the densification of porous substrates with a pyrolytic carbon matrix such as a gas densification process for the manufacture of carbon / carbon materials, for example for the production of discs of brake.
• the precursor gas for this reaction is a hydrocarbon, typically methane, propane, or a mixture of both.
• the reaction pressure and temperature are controlled to produce the pyrolytic carbon coating or matrix by decomposing (cracking) the precursor gas on contact with the substrates.
• oil loaded with PAH or “mixture of oils loaded with PAH” means any oil or mixture of oils according to the invention containing more than 5% by volume of PAH relative to the volume. total oil or mixture of oils. In particular, the total PAH content of the oil or of the mixture of oils is at most 30% by volume.
• the oil or mixture of oils loaded with polycyclic aromatic hydrocarbons according to the invention results from a process for washing effluent gas containing polycyclic aromatic hydrocarbons.
• the effluent gas is advantageously produced by a chemical vapor deposition or infiltration process for the formation of pyrolytic carbon deposition on substrates or for the densification of porous substrates with a pyrolytic carbon matrix such as a gas densification process for the manufacture of carbon / carbon materials, for example for the production of brake discs.
• This effluent gas washing process with aromatic mineral oil or a mixture of aromatic mineral oil and naphthenic mineral oil is well known to those skilled in the art and is for example described in patent applications WO 03 / 047725 and WO 2015/132527. It can thus be carried out by spraying the oil or the mixture of oils into a stream of effluent gas passing through a spray column, for example a venturi column.
• this washing is carried out at a pressure of between lxlO 3 and lxlO 5 Pa, more advantageous at a pressure of lOOOPa (lOmbars absolute), even if such a pressure does not facilitate the condensation of the PAHs, which limits the absorption of the PAHs by the oil.
• this washing process is carried out at a temperature below 20 ° C, advantageously below 0 ° C.
• mineral oil (either that comprising aromatic mineral oil, or that comprising the mixture of aromatic mineral oil and naphthenic mineral oil, depending on the variant used and the process phase) circulates continuously between a recirculation tank collecting mineral oil loaded with polycyclic aromatic hydrocarbons and at least one nozzle for spraying oil in a stream of effluent gas.
• the mineral oil is preferably cooled on its path between the recirculation tank and the spray nozzle (s). In fact, this cooling makes it possible to promote the condensation of the PAHs present in the effluent gas to be treated so that the latter are entrained by the mineral oil during spraying.
• the temperature of the mineral oil on arrival at the spray nozzle is less than 20 ° C, advantageously less than 0 ° C.
• the effluent gas to be treated is not itself cooled before it arrives at the washing place.
• the temperature of the effluent gas to be treated at the time of washing is less than 200 ° C.
• the process for treating the oil or the mixture of oils according to the invention therefore comprises an optional step (a) of removing polycyclic aromatic hydrocarbons having a molecular mass greater than or equal to 200 (heavy PAHs) from the oil.
• aromatic mineral or a mixture of aromatic mineral oil and naphthenic mineral oil loaded with polycyclic aromatic hydrocarbons This step is only present if the aromatic mineral oil or the mixture aromatic mineral oil and naphthenic mineral oil loaded with polycyclic aromatic hydrocarbons contains polycyclic aromatic hydrocarbons with a molecular weight greater than or equal to 200 (heavy PAHs). It can be implemented by methods well known to those skilled in the art, such as for example by decantation, precipitation for example by action on the temperature and / or filtration on a cartridge filter with or without automatic unclogging.
• the process for treating the oil or the mixture of oils according to the invention further comprises a step (b) of extraction at a pressure below atmospheric pressure of polycyclic aromatic hydrocarbons having a molecular mass of less than 200 (PAHs). medium or light) dissolved in the oil or the mixture of oils obtained in step (a).
• PAHs polycyclic aromatic hydrocarbons having a molecular mass of less than 200
• the pressure in step (b) is therefore less than atmospheric pressure, that is to say less than 101 325 Pa.
• the pressure is greater than or equal to 100 Pa, more particularly between 100 and 50,000 Pa. , even more particularly between 100 Pa and 1500 Pa, in particular 100 Pa or 1500 Pa.
• Step (b) is advantageously carried out by generation, in particular in a controlled manner, of a gas phase enriched in polycyclic aromatic hydrocarbons having a molecular mass of less than 200.
• the gas phase enriched in polycyclic aromatic hydrocarbons having a mass molecular weight less than 200 comprises between 1 and 10% by volume of polycyclic aromatic hydrocarbons having a molecular mass less than 200, relative to the total volume of the gas, in particular between 2 and 5% by volume of polycyclic aromatic hydrocarbons having a mass molecular weight less than 200, relative to the total volume of the gas.
• the temperature for carrying out step (b) is advantageously between 0 and 300 ° C, in particular between 10 and 200 ° C, more particularly between 10 and 100 ° C.
• step (b) can consist of a controlled heating at a pressure below atmospheric pressure of the oil or of the mixture of oils at a temperature and a pressure allowing the generation of a vapor rich in polycyclic aromatic hydrocarbons having a molecular mass of less than 200.
• PAHs having a molecular mass of less than 200 are in fact more volatile than the oil or the mixture of oils according to the invention and they leave the liquid oil.
• the oil or the mixture of oils is maintained at a pressure greater than or equal to 100 Pa, more particularly between 100 and 50,000 Pa, even more particularly between 100 Pa and 1500 Pa, in particular 100 Pa or of 1500 Pa.
• the heating takes place at a temperature greater than 120 ° C, advantageously greater than or equal to 130 ° C, in particular between 130 and 300 ° C, more particularly between 130 and 200 ° C, even more particularly between 130 and 150 ° C, more particularly greater than or equal to 140 ° C, still more particularly greater than or equal to 150 ° C.
• Steam contains more PAHs as they have low boiling points. Thus the boiling points of the main PAHs are collated in Table 2 below.
• Table 2 Table 3 below collates the vapor pressures of different PAHs as a function of temperature.
• naphthalene will thus be more entrained in the vapor phase than the acenaphthene, which will itself be more entrained in the vapor phase than the phenanthrene.
• step (b) of the process according to the invention it is also possible to reduce the heating temperature of step (b) of the process according to the invention by using an aromatic compound having a boiling point of less than 100 ° C. at the operating pressure of the process. There is indeed a phenomenon of entrainment of PAHs by the vapor of the aromatic compound.
• the method according to the present invention comprises an intermediate step (a1) between steps (b) and (c) of addition to the oil or to the mixture of oils obtained in step ( a) an aromatic compound having a boiling point less than 100 ° C at the operating pressure of step b), advantageously at a pressure greater than or equal to 100 Pa, more particularly between 100 and 50 000 Pa, even more particularly between 100 Pa and 1500 Pa, in particular 100 Pa or 1500 Pa, and in that step (b) is carried out at a temperature below 120 ° C, advantageously below or equal to 100 ° C, in particular between 40 and 100 ° C, more particularly between 50 and 100 ° C, even more particularly between 60 and 100 ° C, in particular between 70 and 100 ° C, and to a pressure greater than or equal to 100 Pa, more particularly between 100 and 50,000 Pa, even more particularly It is also between 100 Pa and 1500 Pa, in particular 100 Pa or 1500 Pa.
• step (b) of the process for treating the oil or the mixture of oils according to the invention consists of bringing it into contact with stirring, for example by bubbling, and at a pressure lower than the atmospheric pressure of the oil or of the mixture of oils with a non-condensable gas so as to extract the polycyclic aromatic hydrocarbons from the oil or from the mixture of oils.
• the non-condensable gas is an inert gas such as nitrogen, or a hydrocarbon in gaseous form which may optionally contain H 2 OR N 2 , advantageously a hydrocarbon in gaseous form, in particular used in a densification process by means of gas for the manufacture of carbon / carbon materials, such as for example for the production of brake discs.
• it is methane.
• the oil or the mixture of oil to be treated will be heated, for example at a temperature of 50 ° C and at a pressure greater than or equal to 100 Pa, more particularly between 100 and 50,000 Pa, even more particularly between 100 Pa and 1500
• PAH extraction gas in particular 100 Pa or 1500 Pa
• a packed column is an example of equipment allowing this extraction of compounds dissolved in a liquid.
• the extraction gas is usually available under pressure, which allows pressure drops in the column.
• the column can operate in batch or continuous mode. Batch operation is preferred for its simplicity of operation.
• Light PAHs (especially naphthalene) are easily extracted from the oil by this method.
• the quantity of oil carried away is small compared to the cumulative quantity of PAH carried away by the gas such as methane.
• step (b) of the process according to the invention is not a distillation step.
• step (b) of the process according to the invention does not include a distillation step.
• the process according to the invention does not include a distillation stage, in particular a stage of distillation of aromatic mineral oil or of a mixture of aromatic mineral oil and naphthenic mineral oil. .
• the oil or mixture of oils depleted in polycyclic aromatic hydrocarbons obtained in step (c) comprises a maximum of 10% by mass of the initial quantity of polycyclic aromatic hydrocarbons (that is to say of that initially contained ( before the optional step (a)) in aromatic mineral oil or in the mixture of aromatic mineral oil and naphthenic mineral oil), advantageously between 5 and 10% by mass of the initial quantity of polycyclic aromatic hydrocarbons, more preferably at most 5% by mass of the initial amount of polycyclic aromatic hydrocarbons.
• the process according to the invention comprises an additional stage (d) of treatment of the polycyclic aromatic hydrocarbons extracted from the oil or from the mixture of oils according to the invention.
• the treatment of the PAH stream can be thermal oxidation, condensation, adsorption on activated carbon or else use in the pyrocarbon densification process.
• the method according to the invention comprises a preliminary step (A) of generating an aromatic mineral oil or a mixture of aromatic mineral oil and oil.
• naphthenic mineral said oil or said mixture of oils being charged with polycyclic aromatic hydrocarbons, by washing an effluent gas containing polycyclic aromatic hydrocarbons.
• the effluent gas results from a chemical vapor deposition or infiltration process for the formation of pyrolytic carbon deposition on substrates or for the densification of porous substrates with a pyrolytic carbon matrix such as a gas densification process for the manufacture of carbon / carbon materials, for example for the production of brake discs.
• This step of washing an effluent gas with aromatic mineral oil or a mixture of aromatic mineral oil and naphthenic mineral oil is well known to those skilled in the art and is for example described in patent applications WO 03/047725 and WO 2015/132527.
• this washing step is carried out at a pressure between lxlO 3 and lxlO 5 Pa, more advantageously at a pressure of 1000Pa (lOmbars absolute), even if such a pressure does not facilitate the condensation of the PAHs, which limits absorption of PAHs by oil.
• this washing step is carried out at a temperature below 20 ° C, advantageously below 0 ° C.
• mineral oil (either that comprising aromatic mineral oil, or that comprising the mixture of aromatic mineral oil and naphthenic mineral oil, depending on the variant used and the process phase) circulates continuously between a recirculation tank collecting the mineral oil loaded with polycyclic aromatic hydrocarbons and at least an oil spray nozzle in a stream of effluent gas.
• the mineral oil is preferably cooled on its path between the recirculation tank and the spray nozzle (s). In fact, this cooling makes it possible to promote the condensation of the PAHs present in the effluent gas to be treated so that the latter are entrained by the mineral oil during spraying.
• the temperature of the mineral oil on arrival at the spray nozzle is less than 20 ° C, advantageously less than 0 ° C.
• the effluent gas to be treated is not itself cooled before it arrives at the washing place.
• the temperature of the effluent gas to be treated at the time of washing is less than 200 ° C.
• the process according to the invention comprises an additional step (e) of recycling the oil or the mixture of oils depleted in polycyclic aromatic hydrocarbons obtained in step (c) in the step of washing the effluent gas containing polycyclic aromatic hydrocarbons.

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• Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
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• Organic Chemistry (AREA)
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• Mechanical Engineering (AREA)
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• 2019
  • 2019-09-26 FR FR1910651A patent/FR3101256B1/fr active Active
• 2020
  • 2020-09-25 EP EP20790380.8A patent/EP4034612A1/de active Pending
  • 2020-09-25 US US17/642,547 patent/US11753594B2/en active Active
  • 2020-09-25 WO PCT/FR2020/051676 patent/WO2021058922A1/fr not_active Ceased
  • 2020-09-25 CN CN202080067814.0A patent/CN114514062B/zh active Active

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