US20020038482A1 - Use of liquid dyestuff preparations for dyeing wood - Google Patents
Use of liquid dyestuff preparations for dyeing wood Download PDFInfo
- Publication number
- US20020038482A1 US20020038482A1 US09/497,008 US49700800A US2002038482A1 US 20020038482 A1 US20020038482 A1 US 20020038482A1 US 49700800 A US49700800 A US 49700800A US 2002038482 A1 US2002038482 A1 US 2002038482A1
- Authority
- US
- United States
- Prior art keywords
- formula
- weight
- dyestuff
- glycol
- radicals
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 239000000975 dye Substances 0.000 title claims abstract description 43
- 239000002023 wood Substances 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 26
- 239000007788 liquid Substances 0.000 title claims abstract description 22
- 238000004043 dyeing Methods 0.000 title claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000001768 cations Chemical class 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 3
- -1 o-chlorophenylazo group Chemical group 0.000 claims description 11
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 claims description 5
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 claims description 5
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 4
- 230000000536 complexating effect Effects 0.000 claims description 4
- 238000007654 immersion Methods 0.000 claims description 4
- 241000208140 Acer Species 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 230000001680 brushing effect Effects 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229920000151 polyglycol Polymers 0.000 claims description 3
- 239000010695 polyglycol Substances 0.000 claims description 3
- 238000005096 rolling process Methods 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 claims description 2
- ODCMOZLVFHHLMY-UHFFFAOYSA-N 1-(2-hydroxyethoxy)hexan-2-ol Chemical compound CCCCC(O)COCCO ODCMOZLVFHHLMY-UHFFFAOYSA-N 0.000 claims description 2
- MLHQPPYBHZSBCX-UHFFFAOYSA-N 1-(2-hydroxyethoxy)propan-2-ol Chemical compound CC(O)COCCO MLHQPPYBHZSBCX-UHFFFAOYSA-N 0.000 claims description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 2
- DEDUBNVYPMOFDR-UHFFFAOYSA-N 2-ethoxypropan-1-ol Chemical compound CCOC(C)CO DEDUBNVYPMOFDR-UHFFFAOYSA-N 0.000 claims description 2
- YTTFFPATQICAQN-UHFFFAOYSA-N 2-methoxypropan-1-ol Chemical compound COC(C)CO YTTFFPATQICAQN-UHFFFAOYSA-N 0.000 claims description 2
- YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 claims description 2
- VKCROHJIGLNYSC-UHFFFAOYSA-N 3-(3-ethoxypropoxy)propan-1-ol Chemical compound CCOCCCOCCCO VKCROHJIGLNYSC-UHFFFAOYSA-N 0.000 claims description 2
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 claims description 2
- 240000005020 Acaciella glauca Species 0.000 claims description 2
- 235000018185 Betula X alpestris Nutrition 0.000 claims description 2
- 235000018212 Betula X uliginosa Nutrition 0.000 claims description 2
- 235000014036 Castanea Nutrition 0.000 claims description 2
- 241001070941 Castanea Species 0.000 claims description 2
- 240000009226 Corylus americana Species 0.000 claims description 2
- 235000001543 Corylus americana Nutrition 0.000 claims description 2
- 235000007466 Corylus avellana Nutrition 0.000 claims description 2
- 240000000731 Fagus sylvatica Species 0.000 claims description 2
- 235000010099 Fagus sylvatica Nutrition 0.000 claims description 2
- 240000007049 Juglans regia Species 0.000 claims description 2
- 235000009496 Juglans regia Nutrition 0.000 claims description 2
- 241000218652 Larix Species 0.000 claims description 2
- 235000005590 Larix decidua Nutrition 0.000 claims description 2
- 241000218657 Picea Species 0.000 claims description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 claims description 2
- 241000018646 Pinus brutia Species 0.000 claims description 2
- 235000011613 Pinus brutia Nutrition 0.000 claims description 2
- 235000008582 Pinus sylvestris Nutrition 0.000 claims description 2
- 241000219000 Populus Species 0.000 claims description 2
- 235000014443 Pyrus communis Nutrition 0.000 claims description 2
- 240000001987 Pyrus communis Species 0.000 claims description 2
- 241000219492 Quercus Species 0.000 claims description 2
- 235000016976 Quercus macrolepis Nutrition 0.000 claims description 2
- 241000124033 Salix Species 0.000 claims description 2
- 244000186561 Swietenia macrophylla Species 0.000 claims description 2
- 240000002871 Tectona grandis Species 0.000 claims description 2
- 240000007313 Tilia cordata Species 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 claims description 2
- 235000020234 walnut Nutrition 0.000 claims description 2
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 0 C.O=S(=O)(O)*1CO[Cr]2(O[2H]*=NCCO2)OBN=N1 Chemical compound C.O=S(=O)(O)*1CO[Cr]2(O[2H]*=NCCO2)OBN=N1 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 230000035515 penetration Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- ZULLGCPFJARRLH-UHFFFAOYSA-N C.CC1=CC(Cl)=CC=C1O.CC1=CC(S(N)(=O)=O)=CC=C1O.CC1=CC([N+](=O)[O-])=CC=C1O.CC1=CC=CC=C1C(=O)O Chemical compound C.CC1=CC(Cl)=CC=C1O.CC1=CC(S(N)(=O)=O)=CC=C1O.CC1=CC([N+](=O)[O-])=CC=C1O.CC1=CC=CC=C1C(=O)O ZULLGCPFJARRLH-UHFFFAOYSA-N 0.000 description 2
- IHWHLCMOAGWOIQ-UHFFFAOYSA-N CC1=C(O)C=CC2=CC=CC=C21.CC1=CC=C(N2N=C(C)C(C)=C2O)C=C1.CC1=NN(C2=CC=CC=C2)C(O)=C1C Chemical compound CC1=C(O)C=CC2=CC=CC=C21.CC1=CC=C(N2N=C(C)C(C)=C2O)C=C1.CC1=NN(C2=CC=CC=C2)C(O)=C1C IHWHLCMOAGWOIQ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- GWCFTYITFDWLAY-UHFFFAOYSA-N 1-ethylazepan-2-one Chemical compound CCN1CCCCCC1=O GWCFTYITFDWLAY-UHFFFAOYSA-N 0.000 description 1
- GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- MDXTXVUTYJJPPT-UHFFFAOYSA-N C.CC1=CC(C(=O)O)=C(C)C=C1.CC1=CC(C)=C(O)C(C)=C1.CC1=CC(C)=C(O)C(C)=C1.CC1=CC(Cl)=CC(C)=C1O.CC1=CC(O)=C(C)C2=CC=CC=C12.CC1=CC=C2C(=C1)C(C)=CC(O)=C2C Chemical compound C.CC1=CC(C(=O)O)=C(C)C=C1.CC1=CC(C)=C(O)C(C)=C1.CC1=CC(C)=C(O)C(C)=C1.CC1=CC(Cl)=CC(C)=C1O.CC1=CC(O)=C(C)C2=CC=CC=C12.CC1=CC=C2C(=C1)C(C)=CC(O)=C2C MDXTXVUTYJJPPT-UHFFFAOYSA-N 0.000 description 1
- AXPGJVQDFGMUFI-UHFFFAOYSA-J CC1=CC2=C(C=C1)N=NC1=C(O[Cr]3(OC(=O)C4=CC=CC=C4N=CC4=CC(N=NC5=CC(Cl)=CC=C5Cl)=CC=C4O3)OC2=O)N(C2=CC=CC=C2)N=C1C Chemical compound CC1=CC2=C(C=C1)N=NC1=C(O[Cr]3(OC(=O)C4=CC=CC=C4N=CC4=CC(N=NC5=CC(Cl)=CC=C5Cl)=CC=C4O3)OC2=O)N(C2=CC=CC=C2)N=C1C AXPGJVQDFGMUFI-UHFFFAOYSA-J 0.000 description 1
- NDTYIIPBUCWMQN-UHFFFAOYSA-J CC1=CC2=C(C=C1)N=NC1=C(O[Cr]3(OC2=O)OC2=CC=C(N=NC4=CC=C([N+](=O)[O-])C=C4Cl)C=C2C=NC2=C(C=CC(S(N)(=O)=O)=C2)O3)N(C2=CC=CC=C2)N=C1C Chemical compound CC1=CC2=C(C=C1)N=NC1=C(O[Cr]3(OC2=O)OC2=CC=C(N=NC4=CC=C([N+](=O)[O-])C=C4Cl)C=C2C=NC2=C(C=CC(S(N)(=O)=O)=C2)O3)N(C2=CC=CC=C2)N=C1C NDTYIIPBUCWMQN-UHFFFAOYSA-J 0.000 description 1
- PFCAEDHDPKZWCR-UHFFFAOYSA-J CC1=CC2=C(N=NC3=C(C=CC4=CC=CC=C43)O[Cr]3(OC4=CC=C([N+](=O)[O-])C=C4N=NC4=C5C=CC=CC5=CC=C4O3)O2)C2=CC=C([N+](=O)[O-])C=C12 Chemical compound CC1=CC2=C(N=NC3=C(C=CC4=CC=CC=C43)O[Cr]3(OC4=CC=C([N+](=O)[O-])C=C4N=NC4=C5C=CC=CC5=CC=C4O3)O2)C2=CC=C([N+](=O)[O-])C=C12 PFCAEDHDPKZWCR-UHFFFAOYSA-J 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 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
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- ZWXPDGCFMMFNRW-UHFFFAOYSA-N N-methylcaprolactam Chemical compound CN1CCCCCC1=O ZWXPDGCFMMFNRW-UHFFFAOYSA-N 0.000 description 1
- RKMMLQUVSRGFBF-UHFFFAOYSA-J O=S(=O)(O)C1=CC2=C(N=NC3=C(C=CC4=CC=CC=C43)O[Cr]3(OC4=CC=C(Cl)C=C4N=NC4=C5C=CC=CC5=CC=C4O3)O2)C2=CC=CC=C21 Chemical compound O=S(=O)(O)C1=CC2=C(N=NC3=C(C=CC4=CC=CC=C43)O[Cr]3(OC4=CC=C(Cl)C=C4N=NC4=C5C=CC=CC5=CC=C4O3)O2)C2=CC=CC=C21 RKMMLQUVSRGFBF-UHFFFAOYSA-J 0.000 description 1
- VTODJLNXKBBAFU-UHFFFAOYSA-F O=[N+]([O-])C1=CC=C(N=NC2=CC=C3O[Cr]4(OC5=CC=C([N+](=O)[O-])C=C5N=CC3=C2)OC2=C(N=NC3=C(O4)C(S(=O)(=O)O)=CC(Cl)=C3)C3=CC=CC=C3C=C2)C(Cl)=C1.O=[N+]([O-])C1=CC=C(N=NC2=CC=C3O[Cr]4(OC5=CC=C([N+](=O)[O-])C=C5N=CC3=C2)OC2=C(N=NC3=C(O4)C(S(=O)(=O)O)=CC([N+](=O)[O-])=C3)C3=CC=CC=C3C=C2)C(Cl)=C1 Chemical compound O=[N+]([O-])C1=CC=C(N=NC2=CC=C3O[Cr]4(OC5=CC=C([N+](=O)[O-])C=C5N=CC3=C2)OC2=C(N=NC3=C(O4)C(S(=O)(=O)O)=CC(Cl)=C3)C3=CC=CC=C3C=C2)C(Cl)=C1.O=[N+]([O-])C1=CC=C(N=NC2=CC=C3O[Cr]4(OC5=CC=C([N+](=O)[O-])C=C5N=CC3=C2)OC2=C(N=NC3=C(O4)C(S(=O)(=O)O)=CC([N+](=O)[O-])=C3)C3=CC=CC=C3C=C2)C(Cl)=C1 VTODJLNXKBBAFU-UHFFFAOYSA-F 0.000 description 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- MBJUMIJKDKJBBG-UHFFFAOYSA-J [H]N1N=C(C)C2=C1O[Cr]1(OC3=CC=C(Cl)C=C3N=N2)OC2=C(C=C(S(=O)(=O)O)C=C2[N+](=O)[O-])N=NC2=C(O1)N(C1=CC=C(C)C=C1)N=C2C Chemical compound [H]N1N=C(C)C2=C1O[Cr]1(OC3=CC=C(Cl)C=C3N=N2)OC2=C(C=C(S(=O)(=O)O)C=C2[N+](=O)[O-])N=NC2=C(O1)N(C1=CC=C(C)C=C1)N=C2C MBJUMIJKDKJBBG-UHFFFAOYSA-J 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229940006487 lithium cation Drugs 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
- C09B67/0073—Preparations of acid or reactive dyes in liquid form
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19905279A DE19905279A1 (de) | 1999-02-09 | 1999-02-09 | Verwendung flüssiger Farbstoffpräparationen zum Färben von Holz |
DE19905279.4 | 1999-02-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
US20020038482A1 true US20020038482A1 (en) | 2002-04-04 |
Family
ID=7896904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/497,008 Abandoned US20020038482A1 (en) | 1999-02-09 | 2000-02-02 | Use of liquid dyestuff preparations for dyeing wood |
Country Status (3)
Country | Link |
---|---|
US (1) | US20020038482A1 (de) |
EP (1) | EP1027968A3 (de) |
DE (1) | DE19905279A1 (de) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050267539A1 (en) * | 2000-12-21 | 2005-12-01 | Medtronic, Inc. | System and method for ventricular pacing with AV interval modulation |
US20060167506A1 (en) * | 2005-01-21 | 2006-07-27 | Stoop Gustaaf A | Implantable medical device with ventricular pacing protocol |
US20060167508A1 (en) * | 2005-01-21 | 2006-07-27 | Willem Boute | Implantable medical device with ventricular pacing protocol including progressive conduction search |
US20070203523A1 (en) * | 2006-02-28 | 2007-08-30 | Betzold Robert A | Implantable medical device with adaptive operation |
US20070219589A1 (en) * | 2006-01-20 | 2007-09-20 | Condie Catherine R | System and method of using AV conduction timing |
US20070293899A1 (en) * | 2006-06-15 | 2007-12-20 | Sheldon Todd J | System and Method for Ventricular Interval Smoothing Following a Premature Ventricular Contraction |
US20070293900A1 (en) * | 2006-06-15 | 2007-12-20 | Sheldon Todd J | System and Method for Promoting Intrinsic Conduction Through Atrial Timing |
US20070293897A1 (en) * | 2006-06-15 | 2007-12-20 | Sheldon Todd J | System and Method for Promoting Instrinsic Conduction Through Atrial Timing Modification and Calculation of Timing Parameters |
US20070293898A1 (en) * | 2006-06-15 | 2007-12-20 | Sheldon Todd J | System and Method for Determining Intrinsic AV Interval Timing |
US20070299478A1 (en) * | 2004-10-25 | 2007-12-27 | Casavant David A | Self Limited Rate Response |
US20080027490A1 (en) * | 2006-07-31 | 2008-01-31 | Sheldon Todd J | Pacing Mode Event Classification with Rate Smoothing and Increased Ventricular Sensing |
US20080027492A1 (en) * | 2006-07-31 | 2008-01-31 | Sheldon Todd J | Rate Smoothing Pacing Modality with Increased Ventricular Sensing |
US20080027493A1 (en) * | 2006-07-31 | 2008-01-31 | Sheldon Todd J | System and Method for Improving Ventricular Sensing |
US7515958B2 (en) | 2006-07-31 | 2009-04-07 | Medtronic, Inc. | System and method for altering pacing modality |
US7599740B2 (en) | 2000-12-21 | 2009-10-06 | Medtronic, Inc. | Ventricular event filtering for an implantable medical device |
US7689281B2 (en) | 2006-07-31 | 2010-03-30 | Medtronic, Inc. | Pacing mode event classification with increased ventricular sensing |
US7720537B2 (en) | 2006-07-31 | 2010-05-18 | Medtronic, Inc. | System and method for providing improved atrial pacing based on physiological need |
US20100222839A1 (en) * | 2009-02-27 | 2010-09-02 | Medtronic, Inc. | System and method for conditional biventricular pacing |
US20100222834A1 (en) * | 2009-02-27 | 2010-09-02 | Sweeney Michael O | System and method for conditional biventricular pacing |
US20100222838A1 (en) * | 2009-02-27 | 2010-09-02 | Sweeney Michael O | System and method for conditional biventricular pacing |
US7856269B2 (en) | 2006-07-31 | 2010-12-21 | Medtronic, Inc. | System and method for determining phsyiologic events during pacing mode operation |
US20110014414A1 (en) * | 2009-11-06 | 2011-01-20 | Green Rev LLC | Sustainable simulated commodity tropical hardwood panel |
US9931509B2 (en) | 2000-12-21 | 2018-04-03 | Medtronic, Inc. | Fully inhibited dual chamber pacing mode |
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Publication number | Priority date | Publication date | Assignee | Title |
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US7294730B2 (en) * | 2005-11-30 | 2007-11-13 | Xerox Corporation | Colorant compounds |
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DE1901255A1 (de) * | 1969-01-11 | 1970-08-06 | Basf Ag | Verfahren zum Faerben von Holz |
DE2605574C2 (de) * | 1976-02-12 | 1984-01-12 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Chrom- und Kobaltkomplexfarbstoffen und deren Lösungen |
DE2634512C2 (de) * | 1976-07-31 | 1984-11-08 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung konzentrierter, salzarmer Lösungen von sulfonsäuregruppenfreien Kobalt- und Chrom- 1 zu 2-Komplexfarbstoffen |
DE2918634A1 (de) * | 1979-05-09 | 1980-11-20 | Basf Ag | Verfahren zur herstellung von kobalt- und chrom-1 zu 2-komplexfarbstoffen |
DE3121923A1 (de) * | 1981-06-02 | 1982-12-16 | Bayer Ag, 5090 Leverkusen | Asymmetrische 1:2-chromkomplexfarbstoffe |
DE3132334A1 (de) * | 1981-08-17 | 1983-03-03 | Bayer Ag, 5090 Leverkusen | Asymmetrische 1:2-chromkomplexfarbstoffe |
CH660599A5 (de) * | 1984-07-26 | 1987-05-15 | Ciba Geigy Ag | Loesungen anionischer farbstoffe. |
DE4137851A1 (de) * | 1991-11-16 | 1993-05-19 | Basf Ag | Verfahren zum faerben von holzfurnieren |
-
1999
- 1999-02-09 DE DE19905279A patent/DE19905279A1/de not_active Withdrawn
-
2000
- 2000-01-27 EP EP00101606A patent/EP1027968A3/de not_active Withdrawn
- 2000-02-02 US US09/497,008 patent/US20020038482A1/en not_active Abandoned
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US20070299478A1 (en) * | 2004-10-25 | 2007-12-27 | Casavant David A | Self Limited Rate Response |
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US20060167506A1 (en) * | 2005-01-21 | 2006-07-27 | Stoop Gustaaf A | Implantable medical device with ventricular pacing protocol |
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US20070293898A1 (en) * | 2006-06-15 | 2007-12-20 | Sheldon Todd J | System and Method for Determining Intrinsic AV Interval Timing |
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US20100222839A1 (en) * | 2009-02-27 | 2010-09-02 | Medtronic, Inc. | System and method for conditional biventricular pacing |
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Also Published As
Publication number | Publication date |
---|---|
DE19905279A1 (de) | 2000-08-10 |
EP1027968A2 (de) | 2000-08-16 |
EP1027968A3 (de) | 2002-09-18 |
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