NO800207L - Fremgangsmaate ved avfarging av et norbornadien-derivat - Google Patents

Fremgangsmaate ved avfarging av et norbornadien-derivat

Info

Publication number: NO800207L
Authority: NO; Norway
Prior art keywords: clay; dimer; mixture; mixtures; weight ratio
Prior art date: 1979-01-29

Application number

NO800207A

Other languages

English (en)

Norwegian (no)

Inventor

Lewis W Hall Jr

David L Kerr

Elmer J Hollstein

Harry K Myers Jr

Abraham Schneider

Original Assignee

Suntech

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.)

1979-01-29

Filing date

1980-01-28

Publication date

1980-07-30

1980-01-28 Application filed by Suntech filed Critical Suntech

1980-07-30 Publication of NO800207L publication Critical patent/NO800207L/no

Links

238000000034 method Methods 0.000 title claims description 12
239000004927 clay Substances 0.000 claims description 38
239000000539 dimer Substances 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 23
239000000440 bentonite Substances 0.000 claims description 12
229910000278 bentonite Inorganic materials 0.000 claims description 12
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 12
SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 claims description 11
WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 claims description 9
230000002378 acidificating effect Effects 0.000 claims description 8
238000004042 decolorization Methods 0.000 claims description 7
229960000892 attapulgite Drugs 0.000 claims description 6
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 6
229910052625 palygorskite Inorganic materials 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 4
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 4
239000000391 magnesium silicate Substances 0.000 claims description 4
229910052919 magnesium silicate Inorganic materials 0.000 claims description 4
235000019792 magnesium silicate Nutrition 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 2
239000007788 liquid Substances 0.000 description 9
239000003054 catalyst Substances 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
229910052500 inorganic mineral Inorganic materials 0.000 description 7
239000011707 mineral Substances 0.000 description 7
239000000126 substance Substances 0.000 description 6
239000000470 constituent Substances 0.000 description 5
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
238000005984 hydrogenation reaction Methods 0.000 description 4
239000011777 magnesium Substances 0.000 description 4
229910052749 magnesium Inorganic materials 0.000 description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
238000006471 dimerization reaction Methods 0.000 description 3
239000000446 fuel Substances 0.000 description 3
229910052901 montmorillonite Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
238000003756 stirring Methods 0.000 description 3
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004737 colorimetric analysis Methods 0.000 description 2
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000000710 homodimer Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
238000006317 isomerization reaction Methods 0.000 description 2
231100000572 poisoning Toxicity 0.000 description 2
230000000607 poisoning effect Effects 0.000 description 2
239000000047 product Substances 0.000 description 2
238000000746 purification Methods 0.000 description 2
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 1
235000015842 Hesperis Nutrition 0.000 description 1
235000012633 Iberis amara Nutrition 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
238000006352 cycloaddition reaction Methods 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
229910000043 hydrogen iodide Inorganic materials 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical class O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
150000002846 norbornadienes Chemical class 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000003822 preparative gas chromatography Methods 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
239000010703 silicon Substances 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical class CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/62—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
- C07C13/64—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings with a bridged ring system
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/29—Rearrangement of carbon atoms in the hydrocarbon skeleton changing the number of carbon atoms in a ring while maintaining the number of rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/12—Purification; Separation; Use of additives by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Analytical Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Water Supply & Treatment (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Steroid Compounds (AREA)
Saccharide Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

NO800207A 1979-01-29 1980-01-28 Fremgangsmaate ved avfarging av et norbornadien-derivat NO800207L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/007,112 US4229612A (en)	1979-01-29	1979-01-29	Decolorization of norbornadiene dimers

Publications (1)

Publication Number	Publication Date
NO800207L true NO800207L (no)	1980-07-30

Family

ID=21724283

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO800207A NO800207L (no)	1979-01-29	1980-01-28	Fremgangsmaate ved avfarging av et norbornadien-derivat

Country Status (11)

Country	Link
US (1)	US4229612A (da)
JP (1)	JPS55102523A (da)
BE (1)	BE881374A (da)
CA (1)	CA1120065A (da)
DE (1)	DE3003100A1 (da)
DK (1)	DK33880A (da)
FR (1)	FR2447361A1 (da)
GB (1)	GB2040997B (da)
IT (1)	IT1129956B (da)
NL (1)	NL8000510A (da)
NO (1)	NO800207L (da)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4222800A (en) *	1978-11-30	1980-09-16	Suntech, Inc.	Isomerization of endo-endo hexacyclic olefinic dimer of norbornadiene
US4468476A (en) *	1982-06-25	1984-08-28	Conoco Inc.	Color precursor removal from detergent alkyl benzenes
US4426302A (en)	1982-09-24	1984-01-17	Texaco Inc.	Oil recovery method utilizing a dicyclopentadiene derived ethoxysulfonate
US4423278A (en) *	1983-01-17	1983-12-27	Conoco Inc.	Removing color from polyphenylated alkane
US5207894A (en) *	1990-10-12	1993-05-04	Lyondell Petrochemical Company	Removal of aromatic color bodies from aromatic hydrocarbon streams
JPH07206733A (ja) *	1994-01-25	1995-08-08	Maruzen Petrochem Co Ltd	炭化水素化合物およびその製造方法ならびにこの炭化水素化合物を原料とするハロゲン化炭化水素化合物の製造方法およびハロゲン化炭化水素化合物
EP1690457B1 (en) *	2003-12-02	2010-08-11	Kao Corporation	Package drink

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1836577A (en) *	1924-09-29	1931-12-15	Cross Dev Corp	Refining material
US1636938A (en) *	1924-11-11	1927-07-26	Kauffman	Art of decolorizing, clarifying, and purifying petroleum oils
US1838621A (en) *	1926-10-08	1931-12-29	John D Haseman	Solid silicic acid containing bleaching agents and process of making the same
US1866590A (en) *	1928-03-17	1932-07-12	Filtrol Company Of California	Treatment of lubricating oils with an activated clay and water
US1992979A (en) *	1930-11-19	1935-03-05	Gen Chemical Corp	Purification of oils
US3394200A (en) *	1966-02-18	1968-07-23	Atlantic Richfield Co	Method for removing olefins and corrosion bodies from organic compounds

1979
- 1979-01-29 US US06/007,112 patent/US4229612A/en not_active Expired - Lifetime
1980
- 1980-01-09 CA CA000343350A patent/CA1120065A/en not_active Expired
- 1980-01-09 IT IT19112/80A patent/IT1129956B/it active
- 1980-01-24 GB GB7902379A patent/GB2040997B/en not_active Expired
- 1980-01-26 JP JP743880A patent/JPS55102523A/ja active Pending
- 1980-01-28 DK DK33880A patent/DK33880A/da not_active Application Discontinuation
- 1980-01-28 BE BE0/199130A patent/BE881374A/fr not_active IP Right Cessation
- 1980-01-28 NL NL8000510A patent/NL8000510A/nl not_active Application Discontinuation
- 1980-01-28 NO NO800207A patent/NO800207L/no unknown
- 1980-01-29 DE DE19803003100 patent/DE3003100A1/de not_active Withdrawn
- 1980-01-29 FR FR8001855A patent/FR2447361A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
BE881374A (fr)	1980-07-28
FR2447361A1 (fr)	1980-08-22
DK33880A (da)	1980-07-30
DE3003100A1 (de)	1980-08-07
NL8000510A (nl)	1980-07-31
US4229612A (en)	1980-10-21
IT1129956B (it)	1986-06-11
JPS55102523A (en)	1980-08-05
IT8019112A0 (it)	1980-01-09
GB2040997A (en)	1980-09-03
GB2040997B (en)	1983-01-19
CA1120065A (en)	1982-03-16

Publication	Publication Date	Title
US3862900A (en)	1975-01-28	Removal of chemically combined chlorine and other impurities from hydrocarbons
Oppolzer et al.	1973	A New Stereoselective Approach to Substituted Pyrrolidines by Intramolecular Ene‐Reactions. Preliminary communication
NO840485L (no)	1984-08-13	Fremgangsmaate for omdannelse av et c2-c10 alifatisk lineaert olefin til et produkt omfattende hydrokarboner med hoeyt karbontall
US2586889A (en)	1952-02-26	Separation of straight-chain from branched-chain hydrocarbons
Brown et al.	1959	Organoboranes. I. Isomerization and displacement reactions of organoboranes. A convenient procedure for the conversion of internal olefins into primary alcohols
US4524030A (en)	1985-06-18	Process for separating fatty acids
US4524029A (en)	1985-06-18	Process for separating fatty acids
US3352938A (en)	1967-11-14	Olefin double-bond isomerization using a mixture of platinum group metals as a catalyst
EP0134356B1 (en)	1988-03-02	Process for separating fatty acids from rosin acids
US4229612A (en)	1980-10-21	Decolorization of norbornadiene dimers
US2971993A (en)	1961-02-14	Separation of olefinic hydrocarbons with co, ba, k. or ag substituted 10 to 13 angstrom molecular sieves
US4086286A (en)	1978-04-25	Isomerization of tetrahydropolycyclopentadienes to a missile fuel additive
Ralston et al.	1937	The preparation and cracking of high molecular weight nitriles
US2972643A (en)	1961-02-21	Preparation of aromatics from aliphatic olefinic hydrocarbons containing from 2 to 7 carbon atoms per molecule
US3758608A (en)	1973-09-11	Process for acid treating of olefins
GB2036788A (en)	1980-07-02	Isomerization of an endo-endo hexacyclic olefinic dimer ofnorbornadiene
NO129816B (da)	1974-05-27
US3280212A (en)	1966-10-18	Conversion of hydrocarbons
US4225735A (en)	1980-09-30	Isomerization of the hydrogenated norbornadiene endo-endo hexacyclic dimer
US4578223A (en)	1986-03-25	Process for separating saturated fatty acids from each other
JP2823431B2 (ja)	1998-11-11	エピクロロヒドリンの脱色方法
RU2063394C1 (ru)	1996-07-10	Способ выделения дициклопентадиена
US2417872A (en)	1947-03-25	Process for preparing a dimethyl butene from propylene
US3492343A (en)	1970-01-27	Sulphonates
US4286099A (en)	1981-08-25	Sulfolene hydrogenation