JP2020514459A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2020514459A5 JP2020514459A5 JP2019535232A JP2019535232A JP2020514459A5 JP 2020514459 A5 JP2020514459 A5 JP 2020514459A5 JP 2019535232 A JP2019535232 A JP 2019535232A JP 2019535232 A JP2019535232 A JP 2019535232A JP 2020514459 A5 JP2020514459 A5 JP 2020514459A5
- Authority
- JP
- Japan
- Prior art keywords
- extraction
- pah
- raw material
- ring
- solvent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000605 extraction Methods 0.000 claims description 356
- 229930195733 hydrocarbon Natural products 0.000 claims description 240
- 150000002430 hydrocarbons Chemical class 0.000 claims description 240
- 239000002904 solvent Substances 0.000 claims description 238
- 239000004215 Carbon black (E152) Substances 0.000 claims description 226
- -1 heteroatom compound Chemical class 0.000 claims description 211
- 239000002994 raw material Substances 0.000 claims description 194
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 163
- 238000000034 method Methods 0.000 claims description 157
- 229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 claims description 131
- 238000009835 boiling Methods 0.000 claims description 109
- 239000010779 crude oil Substances 0.000 claims description 105
- 125000005842 heteroatom Chemical group 0.000 claims description 94
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 84
- 239000000203 mixture Substances 0.000 claims description 52
- 238000011084 recovery Methods 0.000 claims description 46
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 42
- 239000001569 carbon dioxide Substances 0.000 claims description 42
- 238000004508 fractional distillation Methods 0.000 claims description 40
- 239000003125 aqueous solvent Substances 0.000 claims description 36
- 238000004230 steam cracking Methods 0.000 claims description 34
- 238000004523 catalytic cracking Methods 0.000 claims description 32
- 239000003921 oil Substances 0.000 claims description 32
- 238000004227 thermal cracking Methods 0.000 claims description 25
- 238000004517 catalytic hydrocracking Methods 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 229910001868 water Inorganic materials 0.000 claims description 24
- 238000005194 fractionation Methods 0.000 claims description 22
- 238000011282 treatment Methods 0.000 claims description 20
- 238000005336 cracking Methods 0.000 claims description 18
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 18
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000000010 aprotic solvent Substances 0.000 claims description 14
- 239000002608 ionic liquid Substances 0.000 claims description 13
- 238000000354 decomposition reaction Methods 0.000 claims description 12
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 claims description 12
- UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Natural products C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 11
- 239000003054 catalyst Substances 0.000 claims description 11
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 10
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims description 10
- 238000012545 processing Methods 0.000 claims description 9
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 8
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 8
- 239000010426 asphalt Substances 0.000 claims description 8
- 229930192474 thiophene Natural products 0.000 claims description 8
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 6
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 6
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 6
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims description 6
- 229910021536 Zeolite Inorganic materials 0.000 claims description 5
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 5
- 239000010457 zeolite Substances 0.000 claims description 5
- 230000006837 decompression Effects 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 claims description 3
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 claims description 3
- 238000003795 desorption Methods 0.000 claims description 3
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims description 3
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims description 3
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 2
- BKRRPNHAJPONSH-UHFFFAOYSA-N carbazole Chemical compound C1=CC=C2[C]3C=CC=CC3=NC2=C1 BKRRPNHAJPONSH-UHFFFAOYSA-N 0.000 claims 1
- CXIRWLOIAQYBLZ-UHFFFAOYSA-N nickel(2+);5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Ni+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 CXIRWLOIAQYBLZ-UHFFFAOYSA-N 0.000 claims 1
- 239000012071 phase Substances 0.000 description 81
- 150000001875 compounds Chemical class 0.000 description 54
- 238000000926 separation method Methods 0.000 description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 31
- 230000008569 process Effects 0.000 description 27
- 229910052717 sulfur Inorganic materials 0.000 description 25
- 238000005984 hydrogenation reaction Methods 0.000 description 23
- 239000011593 sulfur Substances 0.000 description 22
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 21
- 125000003118 aryl group Chemical group 0.000 description 19
- 239000000463 material Substances 0.000 description 19
- 229910052799 carbon Inorganic materials 0.000 description 17
- 229910052757 nitrogen Inorganic materials 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 15
- 239000001257 hydrogen Substances 0.000 description 15
- 229910052739 hydrogen Inorganic materials 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 13
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 150000002902 organometallic compounds Chemical class 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000000543 intermediate Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 150000002736 metal compounds Chemical class 0.000 description 9
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 9
- 230000008929 regeneration Effects 0.000 description 9
- 238000011069 regeneration method Methods 0.000 description 9
- 230000002441 reversible effect Effects 0.000 description 9
- 239000000446 fuel Substances 0.000 description 8
- 125000004429 atom Chemical group 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 230000005484 gravity Effects 0.000 description 7
- 125000000623 heterocyclic group Chemical group 0.000 description 7
- 239000012535 impurity Substances 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 7
- 230000002829 reductive effect Effects 0.000 description 7
- 238000012546 transfer Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 6
- 239000003849 aromatic solvent Substances 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 238000000638 solvent extraction Methods 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 5
- 239000000571 coke Substances 0.000 description 5
- 230000009970 fire resistant effect Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920002521 macromolecule Polymers 0.000 description 5
- 238000000197 pyrolysis Methods 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 230000009849 deactivation Effects 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- 239000012847 fine chemical Substances 0.000 description 4
- 230000000670 limiting effect Effects 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 150000002898 organic sulfur compounds Chemical class 0.000 description 4
- 125000002524 organometallic group Chemical group 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 238000007670 refining Methods 0.000 description 4
- 230000008685 targeting Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000003463 adsorbent Substances 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- HDVPIMZXLWNIIP-UHFFFAOYSA-N nickel 5,10,15,20-tetraphenyl-21,23-dihydroporphyrin Chemical compound [Ni].c1cc2nc1c(-c1ccccc1)c1ccc([nH]1)c(-c1ccccc1)c1ccc(n1)c(-c1ccccc1)c1ccc([nH]1)c2-c1ccccc1 HDVPIMZXLWNIIP-UHFFFAOYSA-N 0.000 description 3
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000003586 protic polar solvent Substances 0.000 description 3
- 125000004434 sulfur atom Chemical group 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 238000012864 cross contamination Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000006477 desulfuration reaction Methods 0.000 description 2
- 230000023556 desulfurization Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 239000003915 liquefied petroleum gas Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 150000004395 organic heterocyclic compounds Chemical class 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910003294 NiMo Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 description 1
- GJEAMHAFPYZYDE-UHFFFAOYSA-N [C].[S] Chemical compound [C].[S] GJEAMHAFPYZYDE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000001260 acyclic compounds Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000011959 amorphous silica alumina Substances 0.000 description 1
- 239000002009 anode grade coke Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000013110 organic ligand Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 125000001741 organic sulfur group Chemical group 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 238000010977 unit operation Methods 0.000 description 1
- 238000004148 unit process Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762442003P | 2017-01-04 | 2017-01-04 | |
| US62/442,003 | 2017-01-04 | ||
| PCT/US2018/012172 WO2018129031A1 (en) | 2017-01-04 | 2018-01-03 | Systems and methods for separation and extraction of heterocyclic compounds and polynuclear aromatic hydrocarbons from a hydrocarbon feedstock |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2020514459A JP2020514459A (ja) | 2020-05-21 |
| JP2020514459A5 true JP2020514459A5 (https=) | 2021-02-18 |
Family
ID=61028207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019535232A Pending JP2020514459A (ja) | 2017-01-04 | 2018-01-03 | 炭化水素原料からの複素環式化合物および多核芳香族炭化水素の分離および抽出のためのシステムおよび方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10808186B2 (https=) |
| EP (1) | EP3565872A1 (https=) |
| JP (1) | JP2020514459A (https=) |
| KR (1) | KR102283633B1 (https=) |
| CN (1) | CN110121544B (https=) |
| SA (1) | SA519402063B1 (https=) |
| WO (1) | WO2018129031A1 (https=) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11475318B2 (en) * | 2019-05-29 | 2022-10-18 | Kyndryl, Inc. | Automated resolution of over and under-specification in a knowledge graph |
| CN212275681U (zh) * | 2019-10-28 | 2021-01-01 | 中国石油天然气股份有限公司 | 一种重油四组分自动分离装置 |
| US12544690B2 (en) | 2019-10-28 | 2026-02-10 | Petrochina Company Limited | Automatic separation apparatus for four fractions of heavy oil and separation method thereof |
| US11149213B2 (en) | 2019-12-27 | 2021-10-19 | Saudi Arabian Oil Company | Method to produce light olefins from crude oil |
| US12234418B2 (en) | 2020-08-07 | 2025-02-25 | Carbovate Development Corp. | Hydrocarbon stream separation system and method |
| WO2022029487A1 (en) | 2020-08-07 | 2022-02-10 | Carbovate Development Corp. | Hydrocarbon stream separation system and method |
| US20230374402A1 (en) * | 2020-10-16 | 2023-11-23 | Shell Oil Company | Recovery of aliphatic hydrocarbons |
| AU2023304153A1 (en) * | 2022-07-05 | 2024-11-21 | Evoqua Water Technologies Llc | Use of supercritical carbon dioxide for sorbent extraction |
| FR3163949A1 (fr) * | 2024-06-28 | 2026-01-02 | Safran Landing Systems | Procédé de recyclage d’une huile aromatique de capture chargée en hydrocarbures aromatiques polycycliques |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4746420A (en) | 1986-02-24 | 1988-05-24 | Rei Technologies, Inc. | Process for upgrading diesel oils |
| TW426775B (en) | 1998-03-16 | 2001-03-21 | Ind Tech Res Inst | Method of fibers scouring |
| US6320090B1 (en) | 1999-03-10 | 2001-11-20 | Miami University | Method of removing contaminants from petroleum distillates |
| US6248797B1 (en) | 1999-05-17 | 2001-06-19 | Shelton A. Dias | Supercritical carbon dioxide extraction of contaminants from ion exchange resins |
| US6726832B1 (en) * | 2000-08-15 | 2004-04-27 | Abb Lummus Global Inc. | Multiple stage catalyst bed hydrocracking with interstage feeds |
| US6454932B1 (en) * | 2000-08-15 | 2002-09-24 | Abb Lummus Global Inc. | Multiple stage ebullating bed hydrocracking with interstage stripping and separating |
| JP2006241181A (ja) * | 2005-02-28 | 2006-09-14 | Sekiyu Combinat Kodo Togo Unei Gijutsu Kenkyu Kumiai | 水添脱硫分解プロセス残渣油の冷却用熱交換器のファウリング防止方法 |
| US7566394B2 (en) * | 2006-10-20 | 2009-07-28 | Saudi Arabian Oil Company | Enhanced solvent deasphalting process for heavy hydrocarbon feedstocks utilizing solid adsorbent |
| FR2910487B1 (fr) * | 2006-12-21 | 2010-09-03 | Inst Francais Du Petrole | Procede de conversion de residus incluant 2 desasphaltages en serie |
| JP2008274175A (ja) * | 2007-05-02 | 2008-11-13 | National Institute Of Advanced Industrial & Technology | 炭化水素類の精製法 |
| WO2008154576A1 (en) | 2007-06-11 | 2008-12-18 | Hsm Systems, Inc. | Bitumen upgrading using supercritical fluids |
| US20110144324A1 (en) | 2009-12-14 | 2011-06-16 | Massachusetts Institute Of Technology | Methods and compositions comprising macrocycles |
| EP2542651A4 (en) | 2010-03-01 | 2017-08-23 | Envirollea Inc. | Solvent extraction process to stabilize, desulphurize and dry wide range diesels, stabilized wide range diesels obtained and their uses |
| JP5750508B2 (ja) | 2010-05-17 | 2015-07-22 | ピーティー プルタミナ （ぺルセロ） | 多環芳香族炭化水素含有量が低いプロセスオイルを製造するためのプロセス |
| US8790508B2 (en) | 2010-09-29 | 2014-07-29 | Saudi Arabian Oil Company | Integrated deasphalting and oxidative removal of heteroatom hydrocarbon compounds from liquid hydrocarbon feedstocks |
| US8574426B2 (en) | 2011-12-15 | 2013-11-05 | Uop Llc | Extraction of polycyclic aromatic compounds from petroleum feedstocks using ionic liquids |
| FR2984759B1 (fr) * | 2011-12-22 | 2013-12-20 | IFP Energies Nouvelles | Catalyseur comprenant au moins une zeolithe nu-86, au moins une zeolithe usy et une matrice minerale poreuse et procede d'hydroconversion de charges hydrocarbonees utilisant ce catalyseur |
| CN103214332B (zh) | 2012-01-18 | 2015-03-18 | 中国石油化工股份有限公司 | 由催化裂化柴油生产轻质芳烃和高品质油品的方法 |
| FR3014111B1 (fr) * | 2013-12-03 | 2015-12-25 | IFP Energies Nouvelles | Procede de raffinage d'une charge hydrocarbonee lourde mettant en œuvre un desasphaltage selectif en cascade |
| US8961780B1 (en) * | 2013-12-16 | 2015-02-24 | Saudi Arabian Oil Company | Methods for recovering organic heteroatom compounds from hydrocarbon feedstocks |
| US9169446B2 (en) * | 2013-12-30 | 2015-10-27 | Saudi Arabian Oil Company | Demulsification of emulsified petroleum using carbon dioxide and resin supplement without precipitation of asphaltenes |
| US9688923B2 (en) * | 2014-06-10 | 2017-06-27 | Saudi Arabian Oil Company | Integrated methods for separation and extraction of polynuclear aromatic hydrocarbons, heterocyclic compounds, and organometallic compounds from hydrocarbon feedstocks |
-
2018
- 2018-01-03 KR KR1020197022842A patent/KR102283633B1/ko active Active
- 2018-01-03 CN CN201880005571.0A patent/CN110121544B/zh active Active
- 2018-01-03 WO PCT/US2018/012172 patent/WO2018129031A1/en not_active Ceased
- 2018-01-03 JP JP2019535232A patent/JP2020514459A/ja active Pending
- 2018-01-03 EP EP18701611.8A patent/EP3565872A1/en not_active Withdrawn
- 2018-01-03 US US15/861,105 patent/US10808186B2/en active Active
-
2019
- 2019-07-04 SA SA519402063A patent/SA519402063B1/ar unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2020514459A5 (https=) | ||
| KR102283633B1 (ko) | 탄화수소 공급 원료로부터 복소환형 화합물 및 다핵 방향족 탄화수소의 분리 및 추출을 위한 시스템 및 방법 | |
| EP2084244B1 (en) | Enhanced solvent deasphalting process for heavy hydrocarbon feedstocks utilizing solid adsorbent | |
| KR102233862B1 (ko) | 석유로부터 금속을 제거하는 방법 | |
| JP6564377B2 (ja) | 炭化水素供給原料から有機ヘテロ原子化合物を回収するための方法 | |
| JP6965245B2 (ja) | 蒸気分解処理のための高品質フィードストックを作り出すための方法 | |
| EP3155071B1 (en) | Integrated method for separation and extraction of polynuclear aromatic hydrocarbons, heterocyclic compounds, and organometallic compounds from hydrocarbon feedstocks | |
| CN111484872A (zh) | 一种渣油脱金属方法 | |
| CN103305249A (zh) | 一种生产沥青的方法 | |
| CN112552951A (zh) | 一种适用于低含量芳烃直馏石脑油中芳烃脱除的复合萃取剂及其应用方法 | |
| CN113817496A (zh) | 一种原油或重油预处理方法 | |
| CN103666550A (zh) | 一种焦化汽油蒸汽裂解增产低碳烯烃和芳烃的方法 | |
| CN103664479A (zh) | 一种焦化汽油蒸汽裂解增产低碳烯烃和芳烃的方法 |