DE1026921B - Covering oil for air filter - Google Patents
Covering oil for air filterInfo
- Publication number
- DE1026921B DE1026921B DEN13785A DEN0013785A DE1026921B DE 1026921 B DE1026921 B DE 1026921B DE N13785 A DEN13785 A DE N13785A DE N0013785 A DEN0013785 A DE N0013785A DE 1026921 B DE1026921 B DE 1026921B
- Authority
- DE
- Germany
- Prior art keywords
- mixture according
- oil
- clay
- soluble
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims description 40
- 239000004927 clay Substances 0.000 claims description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 12
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 9
- -1 alkylene glycol Chemical compound 0.000 claims description 9
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical group [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 claims description 9
- 229910000271 hectorite Inorganic materials 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 229940051250 hexylene glycol Drugs 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 229920001083 polybutene Polymers 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 239000007859 condensation product Substances 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 239000010688 mineral lubricating oil Substances 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims 1
- 239000000428 dust Substances 0.000 description 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- FSCNUJMKSQHQSY-UHFFFAOYSA-N Gein Chemical compound COC1=CC(CC=C)=CC=C1OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)CO2)O)O1 FSCNUJMKSQHQSY-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 230000009974 thixotropic effect Effects 0.000 description 2
- ZWPUOFSQNASCII-UHFFFAOYSA-N 1-(2-ethoxyethoxy)butane Chemical compound CCCCOCCOCC ZWPUOFSQNASCII-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- ZUAURMBNZUCEAF-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethanol Chemical compound OCCOCCOC1=CC=CC=C1 ZUAURMBNZUCEAF-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- ZTWQTBDEQSLEAF-UHFFFAOYSA-N C(=O)C=C.N Chemical compound C(=O)C=C.N ZTWQTBDEQSLEAF-UHFFFAOYSA-N 0.000 description 1
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
- KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-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
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- NCXDKOQSCIWPKK-UHFFFAOYSA-N N-heptadecyl-N-methylheptadecan-1-amine hydrochloride Chemical compound Cl.CCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCC NCXDKOQSCIWPKK-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- YDHWWBZFRZWVHO-UHFFFAOYSA-N [hydroxy(phosphonooxy)phosphoryl] phosphono hydrogen phosphate Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(O)=O YDHWWBZFRZWVHO-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- XUFQMVCXVFAWAM-UHFFFAOYSA-M di(heptadecyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCC XUFQMVCXVFAWAM-UHFFFAOYSA-M 0.000 description 1
- RNPXCFINMKSQPQ-UHFFFAOYSA-N dicetyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCCCCCC RNPXCFINMKSQPQ-UHFFFAOYSA-N 0.000 description 1
- JTXUVYOABGUBMX-UHFFFAOYSA-N didodecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCC JTXUVYOABGUBMX-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- FRXGWNKDEMTFPL-UHFFFAOYSA-N dioctadecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCCCCCCCC FRXGWNKDEMTFPL-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- YVAXKXBDKMQASJ-UHFFFAOYSA-N dodecyl hexadecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCC YVAXKXBDKMQASJ-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000005021 gait Effects 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- RNYJXPUAFDFIQJ-UHFFFAOYSA-N hydron;octadecan-1-amine;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH3+] RNYJXPUAFDFIQJ-UHFFFAOYSA-N 0.000 description 1
- KKWUACQXLWHLCX-UHFFFAOYSA-N hydron;tetradecan-1-amine;chloride Chemical compound Cl.CCCCCCCCCCCCCCN KKWUACQXLWHLCX-UHFFFAOYSA-N 0.000 description 1
- TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical compound OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000003137 locomotive effect Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- HGFJKWMMHUYFMC-UHFFFAOYSA-N n,n-dioctyldecan-1-amine;hydron;chloride Chemical compound Cl.CCCCCCCCCCN(CCCCCCCC)CCCCCCCC HGFJKWMMHUYFMC-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- YHIXOVNFGQWPFW-UHFFFAOYSA-N octadecan-1-amine;hydrobromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[NH3+] YHIXOVNFGQWPFW-UHFFFAOYSA-N 0.000 description 1
- UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 1
- UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 1
- 150000004010 onium ions Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- WPPGURUIRLDHAB-UHFFFAOYSA-M triethyl(hexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CC WPPGURUIRLDHAB-UHFFFAOYSA-M 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 229940048102 triphosphoric acid Drugs 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F8/00—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying
- F24F8/10—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying by separation, e.g. by filtering
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/14—Other self-supporting filtering material ; Other filtering material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/30—Particle separators, e.g. dust precipitators, using loose filtering material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0073—Preparation of non-Newtonian sols, e.g. thixotropic solutions
- B01J13/0082—Preparation of non-Newtonian sols, e.g. thixotropic solutions containing an organic phase
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/085—Phosphorus oxides, acids or salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/14—Inorganic compounds or elements as ingredients in lubricant compositions inorganic compounds surface treated with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/06—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
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Description
DEUTSCHESGERMAN
Die Erfindung bezieht sich auf Filter und Filterölgemische zur Anwendung beim Filtrieren von Luft und anderen Gasen. Gegenstand der Erfindung sind in erster Linie thixotrope, gelartige Gemische, an welchen Staub und andere Fremdstoffe haften, wenn sie damit in Berührung kommen. Solche Gemische werden auf Filterunterlagen aufgebracht, welche die Form von Metallsieben, Fasermatten, Glaswolle oder anderen faserigen Stoffen, die in Luftfiltern verwendet werden, haben können.The invention relates to filters and filter oil mixtures for use in filtering air and other gases. The invention relates to primarily thixotropic, gel-like mixtures to which dust and other foreign substances adhere when they are with them come into contact. Such mixtures are applied to filter pads, which have the shape of Metal screens, fiber mats, glass wool or other fibrous materials used in air filters, can have.
Zum Stande der Technik gehören verschiedenartige, ölartige Gemische, welche Seifen, chlorierte Verbindungen, Phosphorverbindungen u. dgl. als Staubfänger und Staubzurückhaltungsmittel bei Anwendung in den verschiedensten Arten von Filtern enthalten. Gemische dieser Art sind nicht befriedigend: erstens weil sie die Neigung haben, von der Filterunterlage abzufließen, insbesondere bei höheren Temperaturen, wodurch die staubbindende Wirkung des Gemisches herabgesetzt wird, zweitens weil sie oft scharfen Geruch aufweisen, drittens in manchen Fällen wegen ihrer Feuergefährlichkeit und viertens weil große Mengen von verdickend wirkenden oder Klebrigkeit bedingenden Mitteln erforderlich sind, welche die Gemische verteuern.The state of the art includes various types of oil-like mixtures, which include soaps, chlorinated compounds, Phosphorus compounds and the like as dust collectors and dust retardants when used in various Types of filters included. Mixtures of this kind are not satisfactory: first, because they have the tendency have to flow away from the filter pad, especially at higher temperatures, thereby reducing the dust-binding Effect of the mixture is diminished, secondly because they often have a pungent odor, thirdly in some Cases because of their flammability and fourthly because of large amounts of thickening or stickiness conditional agents are required, which make the mixtures more expensive.
Es ist nun gefunden worden, daß vorzügliche Luftfilter hergestellt werden können, indem man die Metallsiebe oder faseriges Material von Luftfiltern mit thixotropen, gelartigen Gemischen überzieht, die einen überwiegenden Anteil eines mineralischen Schmieröls aufweisen, das einen synergistisch wirkenden Zusatz in kritischen Mengen enthält, der im wesentlichen aus 0,5 bis 3% eines gegen Wasser widerstandsfähigen, aminierten, oleophilen Tones, welcher mit einer phosphorhaltigen Säure behandelt worden ist, sowie aus 0,5 bis 2 °/0 eines Alkylenglykols oder eines Äthers hiervon und 0,5 bis 5% einer öllöslichen, klebend wirkenden polymeren Verbindung besteht. Die Prozentsätze beziehen sich auf das Gewicht und sind jeweils auf die gesamte Mischung berechnet.It has now been found that excellent air filters can be produced by coating the metal sieves or fibrous material of air filters with thixotropic, gel-like mixtures which have a predominant proportion of a mineral lubricating oil which contains a synergistic additive in critical amounts which is im substantially resistant from 0.5 to 3% of a to water, aminated, which has been treated with a phosphorus acid oleophilic clay, and from 0.5 / 0 thereof, an alkylene glycol or an ether to 2 ° and 0.5 to 5% consists of an oil-soluble, adhesive polymeric compound. The percentages relate to the weight and are calculated on the total mixture.
Der wasserbeständige, oleophile Ton kann hergestellt werden durch Aminieren geeigneter kolloidaler Tone, wie Bentonite, Hectorit, sowie auch von synthetischen Tonen mit Aminoverbindungen, so daß das entstehende Aminogel einen oleophilen Charakter erhält, worauf der genannte oleophile Ton mit einer organischen oder anorganischen, sauren, phosphorhaltigen Verbindung behandelt wird. Gewünschtenfalls kann der Ton zuerst mit einer phosphorhaltigen Säure und dann mit einer Aminoverbindung behandelt werden. Das Endprodukt kann eine Oniumverbindung oder ein Phosphatsalz sein, oder das Amin kann physikalisch auf dem angesäuerten Ton adsorbiert sein, oder es kann ein Gemisch dieser Stoffe vorliegen. Die Amine, welche zum Aminieren von Tonen verwendet werden können, umfassen oberflächenüberzugsöl für LuftfilterThe water-resistant, oleophilic clay can be prepared by aminating suitable colloidal clays such as Bentonite, hectorite, as well as synthetic clays with amino compounds, so that the resulting aminogel acquires an oleophilic character, whereupon said oleophilic clay with an organic or inorganic, acidic, phosphorus-containing compound is treated. If desired, the sound can go first treated with a phosphorus acid and then with an amino compound. The end product can be an onium compound or a phosphate salt, or the amine can be physically acidified on the Clay can be adsorbed, or a mixture of these substances can be present. The amines which are used to aminate Clays that can be used include surface coating oil for air filters
Anmelder:Applicant:
N. V. De Bataafsche Petroleum
Maatschappij, Den HaagNV De Bataafsche Petroleum
Maatschappij, The Hague
Vertreter: Dr. K. Schwarzhans, Patentanwalt,
München 19, Rornanplatz 9Representative: Dr. K. Schwarzhans, patent attorney,
Munich 19, Rornanplatz 9
Beanspruchte Priorität:
V. St. v. Amerika vom 18. Juni 1956Claimed priority:
V. St. v. America June 18, 1956
Jack William Armstrong, Concord, Calif.,
Harold Albert Woods und Charles Edwin Francis,Jack William Armstrong, Concord, Calif.,
Harold Albert Woods and Charles Edwin Francis,
Martinez, Calif. (V. St. Α.),
sind als Erfinder genannt wordenMartinez, Calif. (V. St. Α.),
have been named as inventors
aktive Aminoverbindungen, wie langkettige aliphatisch« Amine mit mindestens 10 und vorzugsweise 10 bis 20 Kohlenstoffatomen im Molekül, z. B. Dodecyl- und Octadecylamin, sowie Salze solcher Amine mit anorganischen oder organischen Säuren und quaternäre Ammoniumsalze, z. B. Tetradecylaminhydrochlorid, Octadecylaminhydrochlorid, Dioctyldecylaminhydrochlorid, Octadecylaminhydrobromid, Octadecylaminacetat, Dioctyldecylaminacetat, 12-Oxystearylaminlactat, Trimethyldodecylammoniumchlorid, Triäthylhexadecylammoniumchlorid und Dimethyldiheptadecylammoniumchlorid. Andere im Rahmen der Erfindung verwendbare Aminoverbindungen sind Acrolein-Ammoniak-Kondensationsprodukte oder Epichlorhydrin-Ammoniak-Kondensationsprodukte, in welchen die Aminogruppen vollständig oder teilweise durch Umsetzung mit organischen Carbonsäuren in Amidogruppen umgewandelt sind. Die zum Ansäuern des Tones verwendeten Säuren umfassen anorganische und organische Säuren des Phosphors, wie phosphorige Säure, Unterphosphorsäure, unterphosphorige Säure, Orthophosphorsäure, Pyrophosphorsäure, Triphosphorsäure, Tetraphosphorsäure, Metaphosphorsäure, Dilaurylhydrogenphosphat, Distearylhydrogenphosphat, Dicetylhydrogenphosphat, Laurylcetylhydrogenphosphat, Stearyldihydrogenphosphat, Lauryldihydrogenphosphat, Dimethylhydrogenphosphat, Dibutylhydrogenphosphat, Tetradecan-1-phosphinsäure, 10-Phenyldecyn-1-phosphorsäure. active amino compounds, such as long-chain aliphatic « Amines having at least 10 and preferably 10 to 20 carbon atoms in the molecule, e.g. B. dodecyl and Octadecylamine, as well as salts of such amines with inorganic or organic acids and quaternary ammonium salts, z. B. tetradecylamine hydrochloride, octadecylamine hydrochloride, dioctyldecylamine hydrochloride, Octadecylamine hydrobromide, octadecylamine acetate, dioctyldecylamine acetate, 12-oxystearylamine lactate, trimethyldodecylammonium chloride, Triethylhexadecylammonium chloride and dimethyldiheptadecylammonium chloride. Others that can be used within the scope of the invention Amino compounds are acrolein-ammonia condensation products or epichlorohydrin-ammonia condensation products, in which the amino groups completely or partially by reaction with organic Carboxylic acids are converted into amido groups. Include the acids used to acidify the clay inorganic and organic acids of phosphorus, such as phosphorous acid, hypophosphoric acid, hypophosphorous Acid, orthophosphoric acid, pyrophosphoric acid, triphosphoric acid, tetraphosphoric acid, metaphosphoric acid, Dilauryl hydrogen phosphate, distearyl hydrogen phosphate, dicetyl hydrogen phosphate, lauryl cetyl hydrogen phosphate, Stearyl dihydrogen phosphate, lauryl dihydrogen phosphate, dimethyl hydrogen phosphate, dibutyl hydrogen phosphate, Tetradecane-1-phosphinic acid, 10-phenyldecyn-1-phosphoric acid.
Der wasserbeständige, aminierte, oleophile Ton, der mit einer phosphorhaltigen Säure behandelt worden ist,The water-resistant, aminated, oleophilic clay that has been treated with a phosphoric acid,
709 957/375709 957/375
3 43 4
liegt in dem Gemisch vorzugsweise in einer Menge von Nachstehend werden Beispiele für die Zusammen-1 bis 2% und besonders zweckmäßig in einer Menge setzung von erfindungsgemäßen Gemischen gegeben, von 1,3 bis 1,5% vor.is preferably in the mixture in an amount of Below are examples of the composition-1 up to 2% and particularly expediently given in an amount of mixtures according to the invention, from 1.3 to 1.5%.
Die folgenden Beispiele erläutern Arbeitsweisen zur Mischung AThe following examples explain working methods for mixture A.
Herstenung des wasserbeständigen Tones. 5 Hectoritton nach Beispiel 4 1,3%Manufacture of water-resistant clay. 5 hectorite clay according to example 4 1.3%
Beispiel 1 Hexylenglykol 1,0%Example 1 hexylene glycol 1.0%
p Polybuten (Molgewicht 20 000) 2,0% p polybutene (molecular weight 20,000) 2.0%
Hectoritton wurde in Wasser unter Bildung eines Mineralöl (400 SUS bei 100° F/38,8° C) 95,7% 2%igen Hydrosols dispergiert. Nach einer Absetzperiode von 12 Stunden wurde das milchige Sol ab- io Mischung BHectorite clay was 95.7% in water to form a mineral oil (400 SUS at 100 ° F / 38.8 ° C) 2% hydrosol dispersed. After a settling period of 12 hours, the milky sol became abio mixture B
gegossen und die Gangart abgetrennt. Der Hectorit Hectoritton nach Beispiel 3 1,3%poured and the gait cut off. The hectorite hectorite clay according to Example 3 1.3%
wurde mit Phosphorsäure angesäuert und dann zwecks Hexylenglykol 1.0%was acidified with phosphoric acid and then for the purpose of hexylene glycol 1.0%
Umwandlung der Gesamtmenge des angesäuerten Tones Polybuten (Molgewicht 20 000) 2',0 %Conversion of the total amount of acidified clay polybutene (molecular weight 20,000) 2 ', 0%
in das Phosphorsalz mit Dimethyldiheptadecylammo- Mineralöl (400 SUS bei 100° F/37,8° C) 95,7%in the phosphorus salt with dimethyldiheptadecylammo- mineral oil (400 SUS at 100 ° F / 37.8 ° C) 95.7%
niumchlorid behandelt. Die Salzform des Aminogels 15treated with sodium chloride. The salt form of the aminogel 15
setzte sich rasch ab und konnte leicht mit Wasser ge- Mischung Csettled quickly and could easily be mixed with water. Mixture C
waschen werden, worauf das Gel zwecks Beseitigung Hectoritton nach Beispiel 4 l,4°/owill wash, whereupon the gel for the purpose of eliminating hectorite clay according to Example 4 l, 4%
der Hauptmenge des Wassers filtriert wurde. Hexylenglykol 1,0 %most of the water was filtered. Hexylene glycol 1.0%
Polybuten (Molgewicht 20 000) 2,0%Polybutene (molecular weight 20,000) 2.0%
Beispiel 2 ao Mineralöl (400 SUS bei 100° F/37,8° C) 95,6%Example 2 ao mineral oil (400 SUS at 100 ° F / 37.8 ° C) 95.6%
Die Arbeitsweise gemäß Beispiel 1 wurde wiederholt, Mischung DThe procedure of Example 1 was repeated, mixture D
wobei aber als aminierendes Mittel Epichlorhydrin- Hectoritton nach Beispiel 2 1,4%but with epichlorohydrin hectorite clay as aminating agent according to Example 2 1.4%
Ammoniak-Kondensationsprodukt an Stelle des Di- Hexylenglykol 1.0%Ammonia condensation product instead of di-hexylene glycol 1.0%
methyldiheptadecylammoniumehlorids verwendet wurde. 25 Polybuten (Molgewicht 20 000) 2,0%methyldiheptadecylammonium chloride was used. 25 polybutene (molecular weight 20,000) 2.0%
Mineralöl (400 SUS bei 100° F/37,8° C) 95,6%Mineral oil (400 SUS at 100 ° F / 37.8 ° C) 95.6%
Beisüiel 3Example 3
Die Wirksamkeit der erfindungsgemäßen Mischung alsThe effectiveness of the mixture according to the invention as
Es wurde gearbeitet wie im Beispiel 1, wobei aber als Überzug für Luftfilter ist aus den nachstehend angeaminierendes Mittel ein Kondensationsprodukt aus 5 Mol 30 führten Daten ersichtlich. Bei Versuch I wurden Farr-Ammoniak und 1 Mol Epichlorhydrin verwendet wurde, Luftfilter (4x4x2 Zoll) mit den zu prüfenden Gein welchem ein Drittel der Aminogruppen durch Um- mischen überzogen und in einem Windkanal der Einsetzung mit Talgfettsäuren in Amidogruppen umgewan- wirkung von Staub in hoher Konzentration (20 g) ausdelt war. gesetzt. Ein für die Untersuchung von Zündkerzen stan-The procedure was as in Example 1, but the coating for air filters is from the aminating elements below Mean a condensation product of 5 moles of 30 lead data can be seen. In Experiment I, Farr's ammonia and 1 mole of epichlorohydrin was used, air filter (4x4x2 inch) with the gein to be tested which one-third of the amino groups are coated by shuffling and put in a wind tunnel with tallow fatty acids in amido groups, the effect of dust in high concentration (20 g) was. set. A standard for the investigation of spark plugs
B eis iel 4 35 äardisierter feiner Staub wurde etwa 10 Minuten mitA large amount of 4 35 aardized fine dust was left with for about 10 minutes
■ einer eingestellten Luftströmung von 520 FPM durch das■ a set air flow of 520 FPM through the
Es wurde entsprechend Beispiel 3 gearbeitet, wobei Filter geführt. Die Mischungen A, B, C und D zeigten aber an Stelle der Talgfettsäuren ein Gemisch von ge- eine Filterwirksamkeit über 60 %. Wenn der Hectoritton sättigten C14- bis C18-Fettsäuren verwendet wurde. in den Mischungen A, B, C oder D durch eine Seife ersetztThe procedure was as in Example 3, with filters being used. The mixtures A, B, C and D, however, instead of the tallow fatty acids, showed a mixture with a filter effectiveness of more than 60%. If the hectorite clay saturated C 14 to C 18 fatty acids was used. in mixtures A, B, C or D replaced by a soap
Die zur Anwendung in den erfindungsgemäßen Ge- 40 wurde, z. B. eine Alkaliseife (Mischung Y), betrug die mischen geeigneten Alkylenglykole werden zugesetzt, um Filterwirksamkeit etwa 35 bis 40 %. das Gelatinieren infolge der möglichen Anwesenheit von Bei dem Adhäsionstest (Versuch II) wurden geteerteThe 40 for use in the invention was, for. B. an alkali soap (Mixture Y), was the Mix suitable alkylene glycols are added to filter efficiency about 35 to 40%. the gelatinization due to the possible presence of the adhesion test (experiment II) were tarred
Wasser zu verhindern. Zu diesen Verbindungen gehören Schweißdrähte von x/16 Zoll (1,6 mm) Durchmesser in Äthylenglykol, Propylenglykol, Hexylenglykol und Ge- die Testmischungen eingetaucht, herausgenommen und mische dieser. Andere Stoffe, die an Stelle der Alkylen- 45 dann 24 Stunden bei 180° F (82° C) senkrecht in einen glykole oder in Verbindung mit solchen benutzt werden Ofen gehängt und darauf wieder gewogen. Das Gewicht können, sind die Äther von Alkylenglykol bzw. Dialkylen- des auf den mit den Gemischen A, B, C und D behandelten glykol, z. B. Äther von Äthylenglykol und Äther von Drähten zurückgehaltenen Rückstandes betrug etwa Diäthylenglykol. In die Gruppe solcher Verbindungen ge- 0,035 g, während auf Drähten, die mit einem öl hörenÄthylenglykohnonoäthyläther.Äthylenglykohnono- 50 (400 SUS bei 100° F/37,8° C) überzogen waren, das 3,4% butyläther, Äthylenglykolmonoäthylbutyläther, Äthylen- Polyäthylen enthielt (Mischung Z), nur 0,008 g zurückglykolmonophenyläther, Diäthylenglykohnonomethyl- gehalten wurden.Prevent water. These connections include x / 16 inch (1.6 mm) diameter weld wires in ethylene glycol, propylene glycol, hexylene glycol, and Ge. The test mixtures are dipped, removed, and mixed. Other substances that are used in place of the alkylene-45 are then hung vertically in a glycol oven for 24 hours at 180 ° F (82 ° C) or in conjunction with such and then weighed again. The weight can be the ethers of alkylene glycol or dialkylenes on the glycol treated with the mixtures A, B, C and D, z. B. ether of ethylene glycol and ether of wires retained residue was about diethylene glycol. In the group of such compounds were 0.035 g, while on wires that were coated with an oil, ethylene glycol monoethyl ether, ethylene glycol mono-50 (400 SUS at 100 ° F / 37.8 ° C), 3.4% butyl ether, ethylene glycol monoethyl butyl ether, ethylene - Contained polyethylene (mixture Z), only 0.008 g of back glycol monophenyl ether, diethylene glycol monomethyl were kept.
äther, Diäthylenglykolmonoäthyläther, Diäthylenglykol- Bei Prüfung in der Praxis an Luftfiltern, welche beiether, diethylene glycol monoethyl ether, diethylene glycol- When tested in practice on air filters, which at
monobutyläther, Diäthylenglykohnonophenyläther u. dgl. Diesellokomotiven verwendet wurden, ergaben die Als Beispiele der Polymerisate können Kohlenwasser- 55 Mischungen A, B, C und D während mehrerer Monate stoffpolymeren genannt werden, wie Polymeren von Öle- vorzügliche Resultate. Diese Mischungen waren selbst finen mit 2 bis 12 Kohlenstoffatomen, einschließlich ali- bei normaler Temperatur leicht auf die Filter aufphatischer und arylaliphatischer Olefine und einschließ- zubringen. Sie zeigte auch bei erhöhten Temperaturen lieh von Homo- und Copolymeren, wie Polyäthylen, Poly- während des Gebrauchs keine Neigung zum Abtropfen von buten, und Mischpolymerisaten aus Styrol mit Alkenen 60 den Filtern. Sie wiesen keinen unangenehmen Geruch und Naturkautschuk. Das Molgewicht der Polymeren auf und hatten bezüglich der Zurückhaltung von Staub liegt im allgemeinen zwischen 10 000 und 500 000. Die eine Wirksamkeit von über 60 %. Handelsübliche Luft-Menge des Polymerisates in der Mischung hegt Vorzugs- filteröle, welche Ölefinpolymerisate und bzw. oder Seifen weise zwischen 1 und 3 Gewichtsprozent. enthielten, zeigten bei der Anwendung in Luftfiltern vonmonobutyl ether, diethylene glycol monophenyl ether and the like As examples of the polymers, hydrocarbon mixtures A, B, C and D can be used for several months Material polymers are called, like polymers of oils - excellent results. These mixtures were themselves finen with 2 to 12 carbon atoms, including ali- at normal temperature, slightly on the filter upward and arylaliphatic olefins and inclusions. It also showed at elevated temperatures borrowed from homo- and copolymers, such as polyethylene, poly- no tendency to drip off during use butene, and copolymers of styrene with alkenes 60 the filters. They did not have an unpleasant odor and natural rubber. The molecular weight of the polymers on and had regarding the retention of dust is generally between 10,000 and 500,000. The effectiveness of over 60%. Commercial air volume of the polymer in the mixture contains preferred filter oils, which olefin polymers and / or soaps wisely between 1 and 3 percent by weight. showed when used in air filters of
Das Basisöl kann von paraffinischen, naphthenischen, 65 Diesellokomotiven eine sehr schlechte Wirksamkeit beasphaltischen oder gemischtbasischen Roherdölen ab- züglich des Zurückhaltens von Staub, sie waren selbst geleitet sein, welche in geeigneter Weise raffiniert sind, bei höheren Temperaturen schwer aufzutragen und und kann bezüglich der Viskosität oder in bezug auf den tropften während des Gebrauches. Siedepunkt im Viskositäts- oder Siedebereich von Gasöl Aus Vorstehendem ist ersichtlich, daß Gemische gemäßThe base oil can beasphaltic with very poor effectiveness from paraffinic, naphthenic, 65 diesel locomotives or mixed base raw oils minus the retention of dust, they were themselves which are appropriately refined, difficult to apply and at higher temperatures and can be in terms of viscosity or in terms of dripping during use. Boiling point in the viscosity or boiling range of gas oil From the above it can be seen that mixtures according to
bis zu schwerem Schmieröl liegen. 70 der Erfindung ein Viskositäts-Temperatur-Verhaltenup to heavy lubricating oil. 70 of the invention shows a viscosity-temperature behavior
zeigen, welches ein leichtes Aufbringen auf die Filtersiebe bei niederen Temperaturen ermöglicht und nach dem Aufbringen auf die Siebe die Beibehaltung einer starken Klebrigkeit bei höheren Temperaturen gewährleistet und das Abtropfen, insbesondere bei hohen Temperaturen, verhindert.show which allows easy application to the filter screens at low temperatures and after application on the sieves the retention of a strong stickiness at higher temperatures ensured and prevents dripping, especially at high temperatures.
Claims (12)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US814237XA | 1956-06-18 | 1956-06-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1026921B true DE1026921B (en) | 1958-03-27 |
Family
ID=22164068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEN13785A Pending DE1026921B (en) | 1956-06-18 | 1957-06-18 | Covering oil for air filter |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE558446A (en) |
DE (1) | DE1026921B (en) |
FR (1) | FR1177332A (en) |
GB (1) | GB814237A (en) |
NL (2) | NL106777C (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6267832B1 (en) * | 1999-08-11 | 2001-07-31 | Aaf International | Method and apparatus for automated manufacture of unit filters |
BE1020515A4 (en) * | 2012-03-06 | 2013-12-03 | Boils Pascal | THE CHIMNEY DEPOLLUANTE. |
-
0
- NL NL218205D patent/NL218205A/xx unknown
- BE BE558446D patent/BE558446A/xx unknown
- NL NL106777D patent/NL106777C/xx active
-
1957
- 1957-06-17 GB GB19048/57A patent/GB814237A/en not_active Expired
- 1957-06-18 FR FR1177332D patent/FR1177332A/en not_active Expired
- 1957-06-18 DE DEN13785A patent/DE1026921B/en active Pending
Also Published As
Publication number | Publication date |
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NL106777C (en) | |
GB814237A (en) | 1959-06-03 |
NL218205A (en) | |
FR1177332A (en) | 1959-04-23 |
BE558446A (en) |
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