NO115362B - - Google Patents

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Info

Publication number: NO115362B
Authority: NO; Norway
Prior art keywords: percent; substance; culture solution; coliformin; per cent
Prior art date: 1957-07-01

Application number

NO146400A

Other languages

English (en)

Norwegian (no)

Inventor

H Hagemeyer

M Edwards

Original Assignee

Eastman Kodak Co

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.)

1957-07-01

Filing date

1962-11-12

Publication date

1968-09-23

1961-12-04 Priority claimed from US156975A external-priority patent/US3254140A/en

1962-11-12 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1968-09-23 Publication of NO115362B publication Critical patent/NO115362B/no

Links

239000000126 substance Substances 0.000 claims description 31
230000000694 effects Effects 0.000 claims description 19
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 16
239000013543 active substance Substances 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
239000005711 Benzoic acid Substances 0.000 claims description 8
238000010521 absorption reaction Methods 0.000 claims description 8
235000010233 benzoic acid Nutrition 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
241000233866 Fungi Species 0.000 claims description 5
238000002955 isolation Methods 0.000 claims description 4
241000894006 Bacteria Species 0.000 claims description 3
239000012153 distilled water Substances 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
238000001914 filtration Methods 0.000 claims 2
238000012986 modification Methods 0.000 claims 2
230000004048 modification Effects 0.000 claims 2
239000003960 organic solvent Substances 0.000 claims 2
230000002745 absorbent Effects 0.000 claims 1
239000002250 absorbent Substances 0.000 claims 1
239000002253 acid Substances 0.000 claims 1
229910052500 inorganic mineral Inorganic materials 0.000 claims 1
239000011707 mineral Substances 0.000 claims 1
238000006386 neutralization reaction Methods 0.000 claims 1
238000001953 recrystallisation Methods 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
235000015097 nutrients Nutrition 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 6
239000005909 Kieselgur Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
229910001868 water Inorganic materials 0.000 description 4
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 3
SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
238000010828 elution Methods 0.000 description 3
239000008103 glucose Substances 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
239000005662 Paraffin oil Substances 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
235000001014 amino acid Nutrition 0.000 description 2
229940024606 amino acid Drugs 0.000 description 2
150000001413 amino acids Chemical class 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000001110 calcium chloride Substances 0.000 description 2
229910001628 calcium chloride Inorganic materials 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000012452 mother liquor Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
238000003756 stirring Methods 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000002023 wood Substances 0.000 description 2
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 1
241000223678 Aureobasidium pullulans Species 0.000 description 1
241001465180 Botrytis Species 0.000 description 1
241000308482 Cadophora fastigiata Species 0.000 description 1
241000308473 Cadophora melinii Species 0.000 description 1
241000222120 Candida <Saccharomycetales> Species 0.000 description 1
241000222122 Candida albicans Species 0.000 description 1
241000222178 Candida tropicalis Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241001149956 Cladosporium herbarum Species 0.000 description 1
241001207508 Cladosporium sp. Species 0.000 description 1
241001337994 Cryptococcus <scale insect> Species 0.000 description 1
241000122864 Fonsecaea pedrosoi Species 0.000 description 1
DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
241001480037 Microsporum Species 0.000 description 1
241001459558 Monographella nivalis Species 0.000 description 1
241000893976 Nannizzia gypsea Species 0.000 description 1
241000181702 Ochrocladosporium elatum Species 0.000 description 1
241001310945 Oidiodendron Species 0.000 description 1
241000642069 Oidiodendron fuscum Species 0.000 description 1
241001310947 Oidiodendron griseum Species 0.000 description 1
239000001888 Peptone Substances 0.000 description 1
108010080698 Peptones Proteins 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
241000235645 Pichia kudriavzevii Species 0.000 description 1
101100172720 Rattus norvegicus Ces1e gene Proteins 0.000 description 1
241000223670 Rhinocladiella atrovirens Species 0.000 description 1
241001674251 Serpula lacrymans Species 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
241000223261 Trichoderma viride Species 0.000 description 1
241000223238 Trichophyton Species 0.000 description 1
241001480048 Trichophyton tonsurans Species 0.000 description 1
241001123669 Verticillium albo-atrum Species 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
150000003868 ammonium compounds Chemical class 0.000 description 1
229960001230 asparagine Drugs 0.000 description 1
235000009582 asparagine Nutrition 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
NGPGDYLVALNKEG-UHFFFAOYSA-N azanium;azane;2,3,4-trihydroxy-4-oxobutanoate Chemical compound [NH4+].[NH4+].[O-]C(=O)C(O)C(O)C([O-])=O NGPGDYLVALNKEG-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
229940095731 candida albicans Drugs 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000010411 cooking Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
244000000008 fungal human pathogen Species 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000007429 general method Methods 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Graft Or Block Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Compounds Of Unknown Constitution (AREA)

NO146400A 1957-07-01 1962-11-12 NO115362B (de)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
US66884057A	1957-07-01	1957-07-01
US2882660A	1960-05-13	1960-05-13
US15200161A	1961-11-13	1961-11-13
US15697461A	1961-12-04	1961-12-04
US156975A US3254140A (en)	1961-12-04	1961-12-04	Propylene-acetylenic hydrocarbon block copolymers and process for preparing same
US04/505,227 US4310639A (en)	1957-07-01	1965-10-26	Polyallomers and process for preparing same

Publications (1)

Publication Number	Publication Date
NO115362B true NO115362B (de)	1968-09-23

Family

ID=27556137

Family Applications (4)

Application Number	Title	Priority Date
NO160512A NO115719B (de)	1957-07-01	1962-11-12
NO146402A NO118630B (de)	1957-07-01	1962-11-12
NO146400A NO115362B (de)	1957-07-01	1962-11-12
NO146401A NO115363B (de)	1957-07-01	1962-11-12

Family Applications Before (2)

Application Number	Title	Priority Date	Filing Date
NO160512A NO115719B (de)	1957-07-01	1962-11-12
NO146402A NO118630B (de)	1957-07-01	1962-11-12

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
NO146401A NO115363B (de)	1957-07-01	1962-11-12

Country Status (10)

Country	Link
US (1)	US4310639A (de)
BE (3)	BE624654A (de)
CH (3)	CH456160A (de)
DE (1)	DE1495565A1 (de)
DK (1)	DK116395B (de)
FR (2)	FR1290523A (de)
GB (4)	GB989724A (de)
NL (3)	NL285401A (de)
NO (4)	NO115719B (de)
SE (2)	SE316013B (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1495055B1 (de) *	1964-02-21	1971-01-07	Avisun Corp	Verfahren zur Herstellung von pentanunloeslichen Blockmischpolymerisaten aus AEthylen und Propylen
DE1495054B1 (de) *	1964-02-21	1971-02-04	Avisun Corp	Verfahren zur Herstellung von in Pentan unloeslichen Blockmischpolymerisaten aus AEthylen und Propylen
DE1495056C2 (de) *	1964-02-25	1973-09-20	Avisun Corp., Philadelphia, Pa. (V.St.A.)	Verfahren zur Herstellung von praktisch kristallinen Blockmischpolymerisaten aus Äthylen und Propylen
US3679775A (en) *	1968-04-03	1972-07-25	Eastman Kodak Co	Olefin polymerization process and catalyst
JPS54139693A (en)	1978-04-21	1979-10-30	Sumitomo Chem Co Ltd	Preparation of propylene-ethylene block copolymer
DE2849114C2 (de) *	1978-11-11	1982-12-23	Hoechst Ag, 6000 Frankfurt	Verfahren zur Herstellung einer Polypropylen-Formmasse und ihre Verwendung zur Herstellung von Formkörpern
DE3417442A1 (de) *	1984-05-11	1985-11-14	Hoechst Ag, 6230 Frankfurt	Polyacetylen-formmasse, verfahren zu ihrer herstellung und ihre verwendung
DE3933695C2 (de) *	1989-10-09	2001-02-08	Hoechst Trespaphan Gmbh	Polypropylenfolie mit guten Hafteigenschaften
CA2311543C (en)	1997-11-21	2008-02-05	Chisso Petrochemical Corporation	Process for the preparation of polypropylene-b-poly(ethylene-co-propylene)
EP1834970B1 (de) *	2006-03-15	2014-05-14	Styrolution GmbH	Ein Verfahren zur Herstellung von Polyolefin-Polyvinylaromatischen-Blockcopolymeren

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3970719A (en) *	1958-01-16	1976-07-20	Phillips Petroleum Company	Preparation of block copolymers
US3529037A (en) *	1966-10-25	1970-09-15	Hugh John Hagemeyer Jr	Polyallomers and process for preparing same

0
- BE BE624652D patent/BE624652A/xx unknown
- NL NL285399D patent/NL285399A/xx unknown
- NL NL285400D patent/NL285400A/xx unknown
- NL NL285401D patent/NL285401A/xx unknown
- BE BE624653D patent/BE624653A/xx unknown
- BE BE624654D patent/BE624654A/xx unknown
1961
- 1961-05-11 GB GB17142/61A patent/GB989724A/en not_active Expired
- 1961-05-12 DE DE19611495565 patent/DE1495565A1/de active Pending
- 1961-05-12 FR FR861567A patent/FR1290523A/fr not_active Expired
1962
- 1962-11-07 CH CH1301262A patent/CH456160A/de unknown
- 1962-11-07 CH CH1301162A patent/CH460351A/de unknown
- 1962-11-09 FR FR914902A patent/FR1416316A/fr not_active Expired
- 1962-11-10 SE SE12073/62A patent/SE316013B/xx unknown
- 1962-11-10 SE SE12072/62A patent/SE316012B/xx unknown
- 1962-11-12 NO NO160512A patent/NO115719B/no unknown
- 1962-11-12 NO NO146402A patent/NO118630B/no unknown
- 1962-11-12 NO NO146400A patent/NO115362B/no unknown
- 1962-11-12 NO NO146401A patent/NO115363B/no unknown
- 1962-11-13 GB GB42853/62A patent/GB1009718A/en not_active Expired
- 1962-11-13 GB GB42860/62A patent/GB993752A/en not_active Expired
- 1962-11-13 CH CH1325262A patent/CH469746A/de unknown
- 1962-11-21 GB GB42859/62A patent/GB1018283A/en not_active Expired
1965
- 1965-10-26 US US04/505,227 patent/US4310639A/en not_active Expired - Lifetime
- 1965-11-19 DK DK596465AA patent/DK116395B/da unknown

Also Published As

Publication number	Publication date
DE1495565A1 (de)	1969-05-14
DK116395B (da)	1970-01-05
NO118630B (de)	1970-01-19
FR1416316A (fr)	1965-11-05
GB993752A (en)	1965-06-02
BE624652A (de)
GB1009718A (en)	1965-11-10
CH456160A (de)	1968-05-15
BE624653A (de)
NL285399A (de)
CH460351A (de)	1968-07-31
GB1018283A (en)	1966-01-26
CH469746A (de)	1969-03-15
FR1290523A (fr)	1962-04-13
BE624654A (de)
NO115719B (de)	1968-11-18
US4310639A (en)	1982-01-12
SE316013B (de)	1969-10-13
SE316012B (de)	1969-10-13
NL285400A (de)
GB989724A (en)	1965-04-22
NO115363B (de)	1968-09-23
NL285401A (de)

Publication	Publication Date	Title
Eckerson	1924	Protein synthesis by plants I. Nitrate reduction
Nakayama et al.	1956	Antimycin A: isolation from a new Streptomyces and activity against rice plant blast fungi
NO115362B (de)	1968-09-23
NO127561B (de)	1973-07-16
Jones	1968	Aqueous extraction of gibberellins from pea
DE2209834B2 (de)	1977-08-25	Herstellung von saccharase- inhibitoren
US4256875A (en)	1981-03-17	Extraction of sennosides
DK145545B (da)	1982-12-06	Polyoxinderivat til anvendelse som plantebeskyttelsesmiddel fremgangsmaade til fremstilling deraf samt fungicid med indhold deraf
Verhoeff et al.	1978	Presence of Endo-Polygalacturonase in Conidia of Botrytis cinerea before and during Germination.
Lie	1964	Nodulation of leguminous plants as affected by root secretions and red light
CN114133346A (zh)	2022-03-04	蒜氨酸和大蒜素联合提取制备方法
Virtanen et al.	1934	Synthesis of sucrose in plant tissue
US2479751A (en)	1949-08-23	Isolation of polygalacturonase
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Crowe et al.	1985	SOLUBILISATION OF NITROGENOUS CONSTITUENTS OF BREWERS'SPENT GRAIN
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Ogura et al.	1966	Studies on chlorophyllase of tea leaves
Preece et al.	1950	CYTOLYSIS IN GERMINATING BARLEY: II. PRELIMINARY STUDY OF ENZYME RELATIONSHIPS
US3423288A (en)	1969-01-21	Process for preparing gentiobiose
Christian et al.	1989	Pea saponins in the Pea-Fusarium solani interaction
US3297526A (en)	1967-01-10	Process for producing coprogen and desferricoprogen
Harman	1973	Deterioration of Stored Pea Seed by Aspergillus ruber: Partial
AUBEL	1921	Chemistry of Vegetable Physiology and Agriculture.
Brickman et al.	1939	Studies on Lignin and Related Compounds. XXXIX. The Ethanolysis of Spruce and Maple Woods
US3058890A (en)	1962-10-16	Process for the preparation of pectolytic enzymes