SK86796A3 - A producing method of amines from mixtures gained by splitting of petroleum fraction - Google Patents

A producing method of amines from mixtures gained by splitting of petroleum fraction Download PDF

Info

Publication number: SK86796A3
Authority: SK; Slovakia
Prior art keywords: amines; formula; preparation; heterogeneous catalysts; acid
Prior art date: 1995-07-04

Application number

SK867-96A

Other languages

English (en)

Slovak (sk)

Inventor

Uwe Dingerdissen

Juergen Herrmann

Karsten Eller

Original Assignee

Basf Ag

Priority date (The priority date 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 date listed.)

1995-07-04

Filing date

1996-07-02

Publication date

1997-01-08

1996-07-02 Application filed by Basf Ag filed Critical Basf Ag

1997-01-08 Publication of SK86796A3 publication Critical patent/SK86796A3/sk

Links

150000001412 amines Chemical class 0.000 title claims abstract description 29
239000003208 petroleum Substances 0.000 title claims abstract description 7
238000000034 method Methods 0.000 title claims description 22
239000000203 mixture Substances 0.000 title claims description 18
239000010457 zeolite Substances 0.000 claims abstract description 20
239000002638 heterogeneous catalyst Substances 0.000 claims abstract description 16
239000002253 acid Substances 0.000 claims abstract description 13
229910000323 aluminium silicate Inorganic materials 0.000 claims abstract description 8
229910019142 PO4 Inorganic materials 0.000 claims abstract description 6
235000021317 phosphate Nutrition 0.000 claims abstract description 6
150000003013 phosphoric acid derivatives Chemical class 0.000 claims abstract description 6
150000004760 silicates Chemical class 0.000 claims abstract description 6
125000003118 aryl group Chemical group 0.000 claims abstract description 4
125000002947 alkylene group Chemical group 0.000 claims abstract description 3
238000003980 solgel method Methods 0.000 claims abstract description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 20
230000008569 process Effects 0.000 claims description 19
238000002360 preparation method Methods 0.000 claims description 11
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 10
229910021529 ammonia Inorganic materials 0.000 claims description 10
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 5
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 5
229910021536 Zeolite Inorganic materials 0.000 claims description 5
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
150000001340 alkali metals Chemical class 0.000 claims description 4
229910052782 aluminium Inorganic materials 0.000 claims description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
239000011230 binding agent Substances 0.000 claims description 4
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 4
229910052723 transition metal Inorganic materials 0.000 claims description 4
150000003624 transition metals Chemical class 0.000 claims description 4
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 3
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
150000001342 alkaline earth metals Chemical class 0.000 claims description 3
IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 claims description 3
229920006395 saturated elastomer Polymers 0.000 claims description 3
150000003335 secondary amines Chemical class 0.000 claims description 3
IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 claims description 3
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
239000011229 interlayer Substances 0.000 claims description 2
239000001282 iso-butane Substances 0.000 claims description 2
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
235000006408 oxalic acid Nutrition 0.000 claims description 2
150000003141 primary amines Chemical class 0.000 claims description 2
229910052761 rare earth metal Inorganic materials 0.000 claims description 2
229910052719 titanium Inorganic materials 0.000 claims description 2
125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 1
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
229910052796 boron Inorganic materials 0.000 claims 1
229910052733 gallium Inorganic materials 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
229910000510 noble metal Inorganic materials 0.000 claims 1
239000010936 titanium Substances 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 abstract description 3
125000003342 alkenyl group Chemical group 0.000 abstract description 2
125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract description 2
125000003710 aryl alkyl group Chemical group 0.000 abstract description 2
238000005336 cracking Methods 0.000 abstract description 2
125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
125000002877 alkyl aryl group Chemical group 0.000 abstract 1
125000000304 alkynyl group Chemical group 0.000 abstract 1
125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
239000003054 catalyst Substances 0.000 description 24
150000001336 alkenes Chemical class 0.000 description 13
238000006243 chemical reaction Methods 0.000 description 11
-1 C 4 hydrocarbons Chemical class 0.000 description 10
229910052751 metal Inorganic materials 0.000 description 8
239000002184 metal Substances 0.000 description 8
238000005576 amination reaction Methods 0.000 description 7
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 7
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 6
230000004048 modification Effects 0.000 description 5
238000012986 modification Methods 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
150000002739 metals Chemical class 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 3
238000000605 extraction Methods 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
238000005342 ion exchange Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
229910002651 NO3 Inorganic materials 0.000 description 2
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
229910004298 SiO 2 Inorganic materials 0.000 description 2
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
238000001354 calcination Methods 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000003776 cleavage reaction Methods 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
230000029087 digestion Effects 0.000 description 2
235000019253 formic acid Nutrition 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
238000004898 kneading Methods 0.000 description 2
238000000465 moulding Methods 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
230000007017 scission Effects 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
241000269350 Anura Species 0.000 description 1
125000004649 C2-C8 alkynyl group Chemical group 0.000 description 1
MEYBTTNZBIRLTI-UHFFFAOYSA-N CCCC.CCCC.CC(C)=C Chemical compound CCCC.CCCC.CC(C)=C MEYBTTNZBIRLTI-UHFFFAOYSA-N 0.000 description 1
229910052684 Cerium Inorganic materials 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229910003902 SiCl 4 Inorganic materials 0.000 description 1
229910010413 TiO 2 Inorganic materials 0.000 description 1
ZGOFOSYUUXVFEO-UHFFFAOYSA-N [Fe+4].[O-][Si]([O-])([O-])[O-] Chemical compound [Fe+4].[O-][Si]([O-])([O-])[O-] ZGOFOSYUUXVFEO-UHFFFAOYSA-N 0.000 description 1
238000010306 acid treatment Methods 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
229910001423 beryllium ion Inorganic materials 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
LFKIGTZUWPXSIH-UHFFFAOYSA-N but-1-ene;2-methylprop-1-ene Chemical compound CCC=C.CC(C)=C LFKIGTZUWPXSIH-UHFFFAOYSA-N 0.000 description 1
MFGFTVOVGWMRMN-UHFFFAOYSA-N butan-2-amine Chemical compound C(C)(CC)N.C(C)(CC)N MFGFTVOVGWMRMN-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
230000002860 competitive effect Effects 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
230000009849 deactivation Effects 0.000 description 1
238000000151 deposition Methods 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000007306 functionalization reaction Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
238000010335 hydrothermal treatment Methods 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
238000012994 industrial processing Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910052746 lanthanum Inorganic materials 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
150000005673 monoalkenes Chemical class 0.000 description 1
QPJSUIGXIBEQAC-UHFFFAOYSA-N n-(2,4-dichloro-5-propan-2-yloxyphenyl)acetamide Chemical compound CC(C)OC1=CC(NC(C)=O)=C(Cl)C=C1Cl QPJSUIGXIBEQAC-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
238000006384 oligomerization reaction Methods 0.000 description 1
125000003884 phenylalkyl group Chemical group 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
239000011148 porous material Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000012545 processing Methods 0.000 description 1
150000002910 rare earth metals Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000005215 recombination Methods 0.000 description 1
230000006798 recombination Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000007873 sieving Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/02—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of hydrogen atoms by amino groups
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Silicates, Zeolites, And Molecular Sieves (AREA)

SK867-96A 1995-07-04 1996-07-02 A producing method of amines from mixtures gained by splitting of petroleum fraction SK86796A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19524240A DE19524240A1 (de)	1995-07-04	1995-07-04	Verfahren zur Herstellung von Aminen aus Gemischen, die man bei der Spaltung von Erdölfraktionen erhält, an Zeolithen, Alumosilikaten oder hydrothermal hergestellten Phosphaten

Publications (1)

Publication Number	Publication Date
SK86796A3 true SK86796A3 (en)	1997-01-08

Family

ID=7765917

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK867-96A SK86796A3 (en)	1995-07-04	1996-07-02	A producing method of amines from mixtures gained by splitting of petroleum fraction

Country Status (6)

Country	Link
US (1)	US5763668A (cs)
EP (1)	EP0752409B1 (cs)
JP (1)	JP3943164B2 (cs)
CZ (1)	CZ291594B6 (cs)
DE (2)	DE19524240A1 (cs)
SK (1)	SK86796A3 (cs)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19601409A1 (de) *	1996-01-17	1997-07-24	Basf Ag	Verfahren zur Herstellung von Aminen aus Olefinen an kristallinen Oxiden auf der Basis von Alumophosphaten mit Faujasit-Struktur
DE19615482A1 (de) *	1996-04-19	1997-10-23	Basf Ag	Verfahren zur Herstellung von Aminen aus Olefinen an mesoporösen Oxiden mit hoher Oberfläche
US6576796B1 (en)	2000-06-28	2003-06-10	Basf Aktiengesellschaft	Process for the preparation of alkylamines
DE10110842A1 (de) *	2001-03-07	2002-09-12	Basf Ag	Verfahren zur Herstellung von n-Butylaminen
DE10155524A1 (de) *	2001-11-12	2003-05-22	Basf Ag	Verfahren zur Herstellung von Ethylamin und Butylamin
DE102005051044A1 (de)	2005-10-25	2007-04-26	Basf Ag	Verfahren zur Herstellung von Alkylaminen durch Umsetzung von Olefinen mit Ammoniak
ATE537138T1 (de)	2008-04-09	2011-12-15	Basf Se	Verfahren zur vorbehandlung von hydroaminierungskatalysatoren
US8529869B2 (en)	2009-04-22	2013-09-10	Basf Se	Catalysts and method for the hydroamination of olefins

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2381470A (en) *	1940-11-13	1945-08-07	Sinclair Refining Co	Production of organic compounds containing nitrogen
US2381709A (en) *	1942-11-05	1945-08-07	Sinclair Refining Co	Production of organic compounds containing nitrogen
US2417893A (en) *	1944-10-12	1947-03-25	Sinclair Refining Co	Production of nitriles and amines
US2417892A (en) *	1944-10-12	1947-03-25	Sinclair Refining Co	Production of amines and nitriles
US4375002A (en) *	1980-05-09	1983-02-22	Air Products And Chemicals, Inc.	Amines via the amination of olefins
MX157137A (es) *	1982-07-30	1988-10-28	Air Prod & Chem	Procedimiento mejorado para la obtencion de alquilaminas
DE3326579A1 (de) *	1983-07-23	1985-01-31	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von aminen
DE3327000A1 (de) *	1983-07-27	1985-02-07	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von aminen
US4536602A (en) *	1984-06-01	1985-08-20	Air Products And Chemicals, Inc.	Amination of olefins using organic acid catalysts
EP0305564A1 (en) *	1987-09-01	1989-03-08	Air Products And Chemicals, Inc.	Amines via the amination of olefins using dealuminated zeolites
DE3940349A1 (de) *	1989-12-06	1991-06-13	Basf Ag	Verfahren zur herstellung von aminen
DE4206992A1 (de) *	1992-03-05	1993-09-09	Akzo Nv	Verfahren zur herstellung von tertiaerem butylamin
CA2086814A1 (en) *	1992-09-08	1994-03-09	Brian L. Benac	Tert-butylamine synthesis over dealuminated y-type zeolites
CA2092964A1 (en) *	1992-12-03	1994-06-04	John Frederick Knifton	Tert-butylamine synthesis over zeolite beta

1995
- 1995-07-04 DE DE19524240A patent/DE19524240A1/de not_active Withdrawn
1996
- 1996-06-27 DE DE59606334T patent/DE59606334D1/de not_active Expired - Lifetime
- 1996-06-27 EP EP96110353A patent/EP0752409B1/de not_active Expired - Lifetime
- 1996-07-02 SK SK867-96A patent/SK86796A3/sk unknown
- 1996-07-03 JP JP17399696A patent/JP3943164B2/ja not_active Expired - Lifetime
- 1996-07-03 US US08/675,731 patent/US5763668A/en not_active Expired - Lifetime
- 1996-07-04 CZ CZ19962001A patent/CZ291594B6/cs not_active IP Right Cessation

Also Published As

Publication number	Publication date
CZ291594B6 (cs)	2003-04-16
DE19524240A1 (de)	1997-01-09
EP0752409B1 (de)	2001-01-17
DE59606334D1 (de)	2001-02-22
JPH09104659A (ja)	1997-04-22
JP3943164B2 (ja)	2007-07-11
EP0752409A3 (de)	1998-05-20
US5763668A (en)	1998-06-09
CZ9602001A3 (en)	1997-03-12
EP0752409A2 (de)	1997-01-08

Publication	Publication Date	Title
KR840001531B1 (ko)	1984-10-04	올레핀의 아미노화에 의한 아민제조방법
CA1218677A (en)	1987-03-03	Preparation of amines
SK86796A3 (en)	1997-01-08	A producing method of amines from mixtures gained by splitting of petroleum fraction
US6350914B1 (en)	2002-02-26	Preparation of amines from olefins over zeolites having an NES structure
US5874621A (en)	1999-02-23	Preparation of amines from olefins over NU-85 zeolites
US5900508A (en)	1999-05-04	Preparation of amines from olefins over zeolites of the type PSH-3, MCM-22, SSZ-25 or mixtures thereof
US6143934A (en)	2000-11-07	Preparation of amines from olefins over boron beta-zeolites
US5877352A (en)	1999-03-02	Preparation of amines from olefins on boron-MCM-22 or ERB-1 zeolites
US5840988A (en)	1998-11-24	Preparation of amines from olefins on zeolites of the MCM-49 or MCM-56 type
US5886226A (en)	1999-03-23	Process for producing amines from olefins on zeolites of types SSZ-33, CIT-1 or mixtures thereof
US5773660A (en)	1998-06-30	Preparation of amines from olefins over hexagonal faujasites
US4929759A (en)	1990-05-29	Production of amines from an olefin and ammonia or a primary or secondary amine
US5739405A (en)	1998-04-14	Preparation of amines from olefins over zeolites of the type SSZ-37
SK86596A3 (en)	1997-03-05	Manufacturing process of amines from olefins on aluminium-beta-zeolites without transition metals and prepared without treatment with halogens
US5786510A (en)	1998-07-28	Preparation of amines from olefins over crystalline oxides based on aluminum phosphates and having faujasite structure
SK86696A3 (en)	1997-01-08	A producing method of amines from olefins over pillared clay
JP3091258B2 (ja)	2000-09-25	環状アルキレンイミンのｎ−アルキル化物の製造法