GB974079A - Process for dry cleaning fibrous materials - Google Patents
Process for dry cleaning fibrous materialsInfo
- Publication number
- GB974079A GB974079A GB4271660A GB4271660A GB974079A GB 974079 A GB974079 A GB 974079A GB 4271660 A GB4271660 A GB 4271660A GB 4271660 A GB4271660 A GB 4271660A GB 974079 A GB974079 A GB 974079A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mol
- acid
- formaldehyde
- urea
- acetic acid
- 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.)
- Expired
Links
- 238000005108 dry cleaning Methods 0.000 title abstract 3
- 239000002657 fibrous material Substances 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 24
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 7
- 229920000877 Melamine resin Polymers 0.000 abstract 6
- 239000004202 carbamide Substances 0.000 abstract 6
- 238000009833 condensation Methods 0.000 abstract 6
- -1 ether carboxylic acids Chemical class 0.000 abstract 6
- 150000003839 salts Chemical class 0.000 abstract 6
- 239000007859 condensation product Substances 0.000 abstract 5
- 159000000000 sodium salts Chemical class 0.000 abstract 5
- 229920001807 Urea-formaldehyde Polymers 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 abstract 3
- NISAHDHKGPWBEM-UHFFFAOYSA-N 2-(4-nonylphenoxy)acetic acid Chemical compound CCCCCCCCCC1=CC=C(OCC(O)=O)C=C1 NISAHDHKGPWBEM-UHFFFAOYSA-N 0.000 abstract 3
- JLJISGDAJLMRBM-UHFFFAOYSA-N 2-phenoxytetradecanoic acid Chemical compound CCCCCCCCCCCCC(C(O)=O)OC1=CC=CC=C1 JLJISGDAJLMRBM-UHFFFAOYSA-N 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 230000005494 condensation Effects 0.000 abstract 3
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 abstract 3
- 239000000047 product Substances 0.000 abstract 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 abstract 2
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001768 cations Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 abstract 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 2
- 229950011008 tetrachloroethylene Drugs 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 abstract 1
- SEOAXAYQIZCZSA-UHFFFAOYSA-N 2-[2,3-di(nonyl)naphthalen-1-yl]oxy-3-hydroxy-2-(hydroxymethyl)propanoic acid Chemical compound C(CCCCCCCC)C=1C(=C(C2=CC=CC=C2C1)OC(C(=O)O)(CO)CO)CCCCCCCCC SEOAXAYQIZCZSA-UHFFFAOYSA-N 0.000 abstract 1
- MZOCIXAAHYRYQL-UHFFFAOYSA-N 2-[2-(hydroxymethyl)-4-nonylphenoxy]acetic acid Chemical compound CCCCCCCCCC1=CC=C(OCC(O)=O)C(CO)=C1 MZOCIXAAHYRYQL-UHFFFAOYSA-N 0.000 abstract 1
- MXQQWAZZSHGIQA-UHFFFAOYSA-N 2-[2-benzyl-4-(hydroxymethyl)phenoxy]acetic acid Chemical compound C(C1=CC=CC=C1)C1=C(OCC(=O)O)C=CC(=C1)CO MXQQWAZZSHGIQA-UHFFFAOYSA-N 0.000 abstract 1
- LWJFKDAXHQXVPF-UHFFFAOYSA-N 2-[4-(hydroxymethyl)-2-(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl)phenoxy]acetic acid Chemical compound C12(C(CC(CC1)C2(C)C)C2=C(OCC(=O)O)C=CC(=C2)CO)C LWJFKDAXHQXVPF-UHFFFAOYSA-N 0.000 abstract 1
- FGHGMLFZBVFNJG-UHFFFAOYSA-N 2-[4-(hydroxymethyl)-2-methylphenoxy]propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(CO)C=C1C FGHGMLFZBVFNJG-UHFFFAOYSA-N 0.000 abstract 1
- ZYLOVVHOSDLUKY-UHFFFAOYSA-N 2-[4-(hydroxymethyl)-2-phenylphenoxy]butanoic acid Chemical compound C1(=CC=CC=C1)C1=C(OC(C(=O)O)CC)C=CC(=C1)CO ZYLOVVHOSDLUKY-UHFFFAOYSA-N 0.000 abstract 1
- SXGISEQOSAKILT-UHFFFAOYSA-N 2-[4-dodecyl-2-(hydroxymethyl)phenoxy]acetic acid Chemical class C(CCCCCCCCCCC)C1=CC(=C(OCC(=O)O)C=C1)CO SXGISEQOSAKILT-UHFFFAOYSA-N 0.000 abstract 1
- OONJOFUTQDFEIF-UHFFFAOYSA-N 2-methyl-2-phenoxyicosanoic acid Chemical class C(CCCCCCCCCCCCCCCCC)C(C(=O)O)(C)OC1=CC=CC=C1 OONJOFUTQDFEIF-UHFFFAOYSA-N 0.000 abstract 1
- BSFGAXRDISAMTN-UHFFFAOYSA-N 2-nonyl-2-phenoxyundecanoic acid Chemical compound C(CCCCCCCC)C(C(=O)O)(OC1=CC=CC=C1)CCCCCCCCC BSFGAXRDISAMTN-UHFFFAOYSA-N 0.000 abstract 1
- DOOVLVLYMFSJOM-UHFFFAOYSA-N 2-phenoxyicosanoic acid Chemical compound C(CCCCCCCCCCCCCCCCC)C(C(=O)O)OC1=CC=CC=C1 DOOVLVLYMFSJOM-UHFFFAOYSA-N 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 1
- LLRNKZLGQCTJBS-UHFFFAOYSA-N C(C)(=O)OOC1=C(C=CC=C1)CCCCCCCCC.[Na] Chemical compound C(C)(=O)OOC1=C(C=CC=C1)CCCCCCCCC.[Na] LLRNKZLGQCTJBS-UHFFFAOYSA-N 0.000 abstract 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 abstract 1
- FTQITGSSOTXEQP-UHFFFAOYSA-N [4,5,6-triamino-1,2,3,4,6-pentakis(hydroxymethyl)triazinan-5-yl]methanol Chemical compound C(O)C1(C(C(N(N(N1CO)CO)CO)(N)CO)(N)CO)N FTQITGSSOTXEQP-UHFFFAOYSA-N 0.000 abstract 1
- HNXURTZIRWNCFN-UHFFFAOYSA-N [4,5,6-triamino-1,2-bis(hydroxymethyl)-4H-triazin-3-yl]methanol Chemical compound C(O)N1N(N(C(=C(C1N)N)N)CO)CO HNXURTZIRWNCFN-UHFFFAOYSA-N 0.000 abstract 1
- ZTFAGUYPEGTRQV-UHFFFAOYSA-N acetic acid [2-[2-(hydroxymethyl)-4-(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl)cyclohexyl]oxy-5-(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl)cyclohexyl]methanol Chemical compound C(C)(=O)O.C12(C(CC(CC1)C2(C)C)C2CC(C(CC2)OC2C(CC(CC2)C2C1(CCC(C2)C1(C)C)C)CO)CO)C ZTFAGUYPEGTRQV-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 238000004140 cleaning Methods 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 229960002449 glycine Drugs 0.000 abstract 1
- 235000013905 glycine and its sodium salt Nutrition 0.000 abstract 1
- 159000000003 magnesium salts Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 150000005217 methyl ethers Chemical class 0.000 abstract 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 abstract 1
- 229950005308 oxymethurea Drugs 0.000 abstract 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011734 sodium Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/02—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents
- D06L1/04—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents combined with specific additives
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF30068A DE1111324B (de) | 1959-12-12 | 1959-12-12 | Reinigungsverstaerker fuer die chemische Reinigung von Fasergut |
Publications (1)
Publication Number | Publication Date |
---|---|
GB974079A true GB974079A (en) | 1964-11-04 |
Family
ID=7093587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4271660A Expired GB974079A (en) | 1959-12-12 | 1960-12-12 | Process for dry cleaning fibrous materials |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE598060A (enrdf_load_stackoverflow) |
CH (1) | CH402250A (enrdf_load_stackoverflow) |
DE (1) | DE1111324B (enrdf_load_stackoverflow) |
GB (1) | GB974079A (enrdf_load_stackoverflow) |
NL (2) | NL258749A (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3927024A (en) * | 1972-02-01 | 1975-12-16 | Nobel Hoechst Chimie | Glycolurile derivatives |
-
0
- BE BE598060D patent/BE598060A/xx unknown
- NL NL278506D patent/NL278506A/xx unknown
- NL NL258749D patent/NL258749A/xx unknown
-
1959
- 1959-12-12 DE DEF30068A patent/DE1111324B/de active Pending
-
1960
- 1960-12-09 CH CH1378160A patent/CH402250A/de unknown
- 1960-12-12 GB GB4271660A patent/GB974079A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3927024A (en) * | 1972-02-01 | 1975-12-16 | Nobel Hoechst Chimie | Glycolurile derivatives |
Also Published As
Publication number | Publication date |
---|---|
CH402250A (de) | 1965-11-15 |
NL278506A (enrdf_load_stackoverflow) | |
BE598060A (enrdf_load_stackoverflow) | |
DE1111324B (de) | 1961-07-20 |
NL258749A (enrdf_load_stackoverflow) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1073256A (en) | New bis-oxazoles,process for their preparation and their use | |
GB1061521A (en) | New hydroxyphenyl-1,3-5-triazines,process for their preparation and their use | |
US2366737A (en) | 1,3-dioxolane modified organic products | |
US2985685A (en) | Alkanolamine aluminates as catalysts for ester redistribution | |
GB974079A (en) | Process for dry cleaning fibrous materials | |
US2198583A (en) | Ether esters of nuclear substituted salicylic acids | |
GB1063797A (en) | Bis-oxazolyl-stilbene compounds and process for their manufacture | |
US2290128A (en) | Esters of glycolic acid | |
US3509049A (en) | Fabric softening and brightening compositions | |
GB888209A (en) | 2:5-di[-benzimidazyl-(2)]-furanes | |
US3076020A (en) | New derivatives of 1, 4-bis-styrylbenzene and optical brightening therewith | |
GB853129A (en) | New pyrrolo derivatives and process for their manufacture | |
JPH03504386A (ja) | 2‐アルキルイミダゾリン類のトルエンスルホン酸塩 | |
US2357594A (en) | Esters | |
US2425287A (en) | Aryl carboxyguanamines | |
US2364737A (en) | Ethers | |
US2234374A (en) | Ether esters of halogenated salicylic acids | |
US2778834A (en) | Substituted glycinamides | |
US2372808A (en) | Esters of poly-beta-carboxyalkyl ethers of polyhydric alcohols | |
US2438961A (en) | Gamma-acetyl pimelic acid and diesters thereof | |
GB803361A (en) | A process and products for the improvement of the optical properties of organic material | |
GB1071818A (en) | Novel indane derivatives and processes for their preparation | |
GB978547A (en) | New thiophene derivatives, process for their preparation and their use | |
US2815345A (en) | Quaternary morpholinium phosphites | |
GB805586A (en) | Plasticised linear aromatic polyester compositions |