CH109260A - Faucheuse à moteur. - Google Patents

Faucheuse à moteur.

Info

Publication number: CH109260A
Authority: CH; Switzerland
Prior art keywords: sep; dye; compounds; wool; group
Prior art date: 1924-02-20

Application number

Other languages

German (de)

English (en)

Inventor

Andre Paul

Original Assignee

Andre Paul

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.)

1924-02-20

Filing date

1924-02-20

Publication date

1925-03-16

1924-02-20 Application filed by Andre Paul filed Critical Andre Paul

1925-03-16 Publication of CH109260A publication Critical patent/CH109260A/fr

Links

239000000975 dye Substances 0.000 claims description 43
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 21
238000000034 method Methods 0.000 claims description 21
239000011651 chromium Substances 0.000 claims description 15
210000002268 wool Anatomy 0.000 claims description 14
238000004043 dyeing Methods 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 10
230000002378 acidificating effect Effects 0.000 claims description 8
239000007859 condensation product Substances 0.000 claims description 8
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 7
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 6
229910052804 chromium Inorganic materials 0.000 claims description 6
-1 cobalt complex compounds Chemical class 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
125000000542 sulfonic acid group Chemical group 0.000 claims description 6
239000000987 azo dye Substances 0.000 claims description 5
229920000151 polyglycol Polymers 0.000 claims description 5
239000010695 polyglycol Substances 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 4
150000004696 coordination complex Chemical class 0.000 claims description 3
125000001033 ether group Chemical group 0.000 claims description 2
239000002657 fibrous material Substances 0.000 claims description 2
239000012188 paraffin wax Substances 0.000 claims 1
230000003381 solubilizing effect Effects 0.000 claims 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 17
239000000047 product Substances 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
239000000203 mixture Substances 0.000 description 8
238000009835 boiling Methods 0.000 description 7
229910017464 nitrogen compound Inorganic materials 0.000 description 7
150000002830 nitrogen compounds Chemical class 0.000 description 7
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 7
239000007795 chemical reaction product Substances 0.000 description 6
239000000835 fiber Substances 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
239000003513 alkali Substances 0.000 description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
239000003086 colorant Substances 0.000 description 4
239000000434 metal complex dye Substances 0.000 description 4
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 3
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
238000009833 condensation Methods 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
VPNOHCYAOXWMAR-UHFFFAOYSA-N docosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCN VPNOHCYAOXWMAR-UHFFFAOYSA-N 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
BUHXFUSLEBPCEB-UHFFFAOYSA-N icosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN BUHXFUSLEBPCEB-UHFFFAOYSA-N 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
229910000148 ammonium phosphate Inorganic materials 0.000 description 2
235000019289 ammonium phosphates Nutrition 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
150000001555 benzenes Chemical class 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000005494 condensation Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000009940 knitting Methods 0.000 description 2
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 2
125000005429 oxyalkyl group Chemical group 0.000 description 2
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
238000006277 sulfonation reaction Methods 0.000 description 2
QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
PNXAPWZUZUZMDA-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid;sodium Chemical compound [Na].C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PNXAPWZUZUZMDA-UHFFFAOYSA-N 0.000 description 1
XGRZWVWRMKAQNU-UHFFFAOYSA-K 2-carboxyphenolate;chromium(3+) Chemical compound [Cr+3].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O XGRZWVWRMKAQNU-UHFFFAOYSA-K 0.000 description 1
GJBZRASGBXVGID-UHFFFAOYSA-N 2-heptadecyl-1-methylbenzimidazole Chemical compound C1=CC=C2N(C)C(CCCCCCCCCCCCCCCCC)=NC2=C1 GJBZRASGBXVGID-UHFFFAOYSA-N 0.000 description 1
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 1
NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052977 alkali metal sulfide Inorganic materials 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
235000019257 ammonium acetate Nutrition 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000012752 auxiliary agent Substances 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229940044175 cobalt sulfate Drugs 0.000 description 1
229910000361 cobalt sulfate Inorganic materials 0.000 description 1
KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
238000004040 coloring Methods 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
239000004744 fabric Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
DXRFSTNITSDOKK-UHFFFAOYSA-N formaldehyde;sulfurous acid Chemical compound O=C.OS(O)=O DXRFSTNITSDOKK-UHFFFAOYSA-N 0.000 description 1
BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000000463 material Substances 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
VVXPDWRMIXEULT-UHFFFAOYSA-N octadecan-1-amine;oxirane Chemical compound C1CO1.CCCCCCCCCCCCCCCCCCN VVXPDWRMIXEULT-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
229920006306 polyurethane fiber Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
239000003760 tallow Substances 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
239000004753 textile Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01D—HARVESTING; MOWING
- A01D34/00—Mowers; Mowing apparatus of harvesters
- A01D34/01—Mowers; Mowing apparatus of harvesters characterised by features relating to the type of cutting apparatus
- A01D34/02—Mowers; Mowing apparatus of harvesters characterised by features relating to the type of cutting apparatus having reciprocating cutters
- A01D34/125—Mowers; Mowing apparatus of harvesters characterised by features relating to the type of cutting apparatus having reciprocating cutters with means for discharging mown material

Landscapes

Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Coloring (AREA)

CH109260D 1924-02-20 1924-02-20 Faucheuse à moteur. CH109260A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH109260T		1924-02-20

Publications (1)

Publication Number	Publication Date
CH109260A true CH109260A (fr)	1925-03-16

Family

ID=4368257

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH109260D CH109260A (fr)	1924-02-20	1924-02-20	Faucheuse à moteur.

Country Status (1)

Country	Link
CH (1)	CH109260A (fr)

1924
- 1924-02-20 CH CH109260D patent/CH109260A/fr unknown

Publication	Publication Date	Title
EP0061670A1 (fr)	1982-10-06	Procédé de teinture de cuir et de peaux avec des mélanges de colorants
DE1593978C3 (de)	1974-12-19	Verfahren zur Herstellung sulfonsäuregruppenhaltiger Sulfone
CH640160A5 (de)	1983-12-30	Kokille mit kernzug.
EP0558450B1 (fr)	1999-03-17	Procédé pour teindre du cuir avec des mélanges de colorants
EP0163608B1 (fr)	1988-09-07	Procédé de teinture de matières fibreuses en polyamides naturelles ou synthétiques avec des colorants à complexes métallifères 1:1
CH109260A (fr)	1925-03-16	Faucheuse à moteur.
CH385789A (de)	1964-09-15	Verfahren zum Färben von Wolle mit 1:2-Metallkomplexfarbstoffen
DE2653284B2 (de)	1978-09-07	Verfahren zum gleichmäßigen Farben von synthetischen Fasermaterialien
DE1260427B (de)	1968-02-08	Verfahren zum Faerben von Wolle
DE1099494B (de)	1961-02-16	Verfahren zur Fertigstellung von Faerbungen, welche in saurem Bade auf stickstoffhaltigen Fasern mit im Bad loeslichen Farbstoffen, die mindestens ein bewegliches, mit den Fasern reaktionsfaehiges Halogenatom enthalten, hergestellt worden sind
AT228733B (de)	1963-08-12	Verfahren zum Färben von Wolle
DE4330283A1 (de)	1994-03-10	Stabilisierung von Färbungen auf Polyamidfasern
DE971896C (de)	1959-04-09	Verfahren zur Herstellung kobalthaltiger Azofarbstoffe
DE2504929C2 (de)	1983-04-21	Verfahren zum einstufigen Färben von Mischungen aus Polyamid- und Polyacrylnitril-Fasern
DE1262211B (de)	1968-03-07	Verfahren zum Faerben von Wolle
DE4215589A1 (de)	1993-11-18	Färbeverfahren
DE2056009C (de)	1973-05-24	Verfahren zum gleichmäßigen und streifenfreien Färben von synthetischem Polyamidfasermaterial
DE1057061B (de)	1959-05-14	Verfahren zur Erzeugung von wasserunloeslichen Azofarbstoffen auf pflanzlichen Fasern
DE80421C (fr)
DE87003C (fr)
DE1008254B (de)	1957-05-16	Verfahren zum Faerben stickstoffhaltiger Fasern
DE2542007C3 (de)	1979-07-12	Verfahren zum Färben von natürlichen und synthetischen Polyamidfasern
DE725211C (de)	1942-09-17	Verfahren zum Faerben von Leder
AT230320B (de)	1963-12-10	Verfahren zum Egalisieren von Färbungen auf Wolle und wollähnlichen Fasern und Mittel zur Durchführung des Verfahrens
DE1953069C3 (de)	1973-11-22	Oxalkylierungsprodukte von Bis (2 hydroxy 3 alkoxy propylaminen und deren Verwendung