CH239864A - Dispositif d'attache pour lier les boeufs. - Google Patents
Dispositif d'attache pour lier les boeufs.Info
- Publication number
- CH239864A CH239864A CH239864DA CH239864A CH 239864 A CH239864 A CH 239864A CH 239864D A CH239864D A CH 239864DA CH 239864 A CH239864 A CH 239864A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- dye
- dyes
- benzothiazolylazo
- textile fibers
- Prior art date
Links
- 241000283725 Bos Species 0.000 title 1
- 239000000835 fiber Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- 238000004043 dyeing Methods 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 239000004753 textile Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 229920013639 polyalphaolefin Polymers 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000004711 α-olefin Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- VGPIPTOYYXBMFP-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yldiazenyl)-4-methylphenol Chemical compound CC1=CC=C(O)C(N=NC=2SC3=CC=CC=C3N=2)=C1 VGPIPTOYYXBMFP-UHFFFAOYSA-N 0.000 claims 2
- 239000000975 dye Substances 0.000 description 26
- -1 benzothiazolyl monoazo Chemical group 0.000 description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 6
- 239000002657 fibrous material Substances 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical compound C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 238000004040 coloring Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000986 disperse dye Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 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 3
- 239000000049 pigment Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002816 nickel compounds Chemical class 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- LMHWUYUKNPHNKG-UHFFFAOYSA-N 4-[(6-nitro-1,3-benzothiazol-2-yl)diazenyl]benzene-1,3-diol Chemical compound [N+](=O)([O-])C1=CC2=C(N=C(S2)N=NC2=C(C=C(O)C=C2)O)C=C1 LMHWUYUKNPHNKG-UHFFFAOYSA-N 0.000 description 1
- PBKFYZMSNJCLOA-UHFFFAOYSA-N 4-bromo-6-methyl-1,3-benzothiazol-2-amine Chemical compound CC1=CC(Br)=C2N=C(N)SC2=C1 PBKFYZMSNJCLOA-UHFFFAOYSA-N 0.000 description 1
- OEQQFQXMCPMEIH-UHFFFAOYSA-N 4-chloro-1,3-benzothiazol-2-amine Chemical compound C1=CC=C2SC(N)=NC2=C1Cl OEQQFQXMCPMEIH-UHFFFAOYSA-N 0.000 description 1
- YEBCRAVYUWNFQT-UHFFFAOYSA-N 4-methoxy-1,3-benzothiazol-2-amine Chemical compound COC1=CC=CC2=C1N=C(N)S2 YEBCRAVYUWNFQT-UHFFFAOYSA-N 0.000 description 1
- AHSSHSODSGGVBG-UHFFFAOYSA-N 4-methyl-6-nitro-1,3-benzothiazol-2-amine Chemical compound CC1=CC([N+]([O-])=O)=CC2=C1N=C(N)S2 AHSSHSODSGGVBG-UHFFFAOYSA-N 0.000 description 1
- AVVSRALHGMVQQW-UHFFFAOYSA-N 5-chloro-1,3-benzothiazol-2-amine Chemical compound ClC1=CC=C2SC(N)=NC2=C1 AVVSRALHGMVQQW-UHFFFAOYSA-N 0.000 description 1
- UZJMSFZHPMSAHI-UHFFFAOYSA-N 6-butoxy-1,3-benzothiazol-2-amine Chemical compound CCCCOC1=CC=C2N=C(N)SC2=C1 UZJMSFZHPMSAHI-UHFFFAOYSA-N 0.000 description 1
- VMNXKIDUTPOHPO-UHFFFAOYSA-N 6-chloro-1,3-benzothiazol-2-amine Chemical compound C1=C(Cl)C=C2SC(N)=NC2=C1 VMNXKIDUTPOHPO-UHFFFAOYSA-N 0.000 description 1
- KOYJWFGMEBETBU-UHFFFAOYSA-N 6-ethoxy-1,3-benzothiazol-2-amine Chemical compound CCOC1=CC=C2N=C(N)SC2=C1 KOYJWFGMEBETBU-UHFFFAOYSA-N 0.000 description 1
- CJLUXPZQUXVJNF-UHFFFAOYSA-N 6-fluoro-1,3-benzothiazol-2-amine Chemical compound C1=C(F)C=C2SC(N)=NC2=C1 CJLUXPZQUXVJNF-UHFFFAOYSA-N 0.000 description 1
- ZYHNHJAMVNINSY-UHFFFAOYSA-N 6-methylsulfonyl-1,3-benzothiazol-2-amine Chemical compound CS(=O)(=O)C1=CC=C2N=C(N)SC2=C1 ZYHNHJAMVNINSY-UHFFFAOYSA-N 0.000 description 1
- GPNAVOJCQIEKQF-UHFFFAOYSA-N 6-nitro-1,3-benzothiazol-2-amine Chemical compound C1=C([N+]([O-])=O)C=C2SC(N)=NC2=C1 GPNAVOJCQIEKQF-UHFFFAOYSA-N 0.000 description 1
- JKQDAIVDZXQKCT-UHFFFAOYSA-N 6-propan-2-yl-1,3-benzothiazol-2-amine Chemical compound CC(C)C1=CC=C2N=C(N)SC2=C1 JKQDAIVDZXQKCT-UHFFFAOYSA-N 0.000 description 1
- ZIYXGFFFCFDPJS-UHFFFAOYSA-N 6-propylsulfanyl-1,3-benzothiazol-2-amine Chemical compound CCCSC1=CC=C2N=C(N)SC2=C1 ZIYXGFFFCFDPJS-UHFFFAOYSA-N 0.000 description 1
- YRSGNOGBXBIUNI-UHFFFAOYSA-N CCOC(C=C1)=CC2=C1N=C(N=NC(C=C(C=C1)OCC)=C1O)S2 Chemical compound CCOC(C=C1)=CC2=C1N=C(N=NC(C=C(C=C1)OCC)=C1O)S2 YRSGNOGBXBIUNI-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- FJCHYJKFVPJSEZ-UHFFFAOYSA-N N,N-dimethyl-2H-1,3-benzothiazole-3-sulfonamide Chemical compound CN(S(=O)(=O)N1CSC2=C1C=CC=C2)C FJCHYJKFVPJSEZ-UHFFFAOYSA-N 0.000 description 1
- KNCKWHXERVFSQH-UHFFFAOYSA-N NC=1SC2=C(N1)C(=CC(=C2Br)OC)Br Chemical compound NC=1SC2=C(N1)C(=CC(=C2Br)OC)Br KNCKWHXERVFSQH-UHFFFAOYSA-N 0.000 description 1
- MOPRJQMXVIAFDU-UHFFFAOYSA-N OC1=C(C=C(C=C1)C)N=NC=1SC2=C(N1)C=CC(=C2)OCC Chemical compound OC1=C(C=C(C=C1)C)N=NC=1SC2=C(N1)C=CC(=C2)OCC MOPRJQMXVIAFDU-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/79—Polyolefins
- D06P3/795—Polyolefins using metallisable or mordant dyes, dyeing premetallised fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B68—SADDLERY; UPHOLSTERY
- B68B—HARNESS; DEVICES USED IN CONNECTION THEREWITH; WHIPS OR THE LIKE
- B68B3/00—Traction harnesses; Traction harnesses combined with devices referred to in group B68B1/00
- B68B3/02—Yokes
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR239864X | 1942-09-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH239864A true CH239864A (fr) | 1945-11-15 |
Family
ID=8883183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH239864D CH239864A (fr) | 1942-09-21 | 1943-09-20 | Dispositif d'attache pour lier les boeufs. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH239864A (fr) |
-
1943
- 1943-09-20 CH CH239864D patent/CH239864A/fr unknown
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