DD211354A5 - Verwendung von saeuregruppen enthaltenden thermostabilen, hydrophilen kondensationsprodukten von aldehyden und ketonen - Google Patents
Verwendung von saeuregruppen enthaltenden thermostabilen, hydrophilen kondensationsprodukten von aldehyden und ketonen Download PDFInfo
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- DD211354A5 DD211354A5 DD82255303A DD25530382A DD211354A5 DD 211354 A5 DD211354 A5 DD 211354A5 DD 82255303 A DD82255303 A DD 82255303A DD 25530382 A DD25530382 A DD 25530382A DD 211354 A5 DD211354 A5 DD 211354A5
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- German Democratic Republic
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- ketone
- condensation products
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- 239000007859 condensation product Substances 0.000 title claims abstract description 71
- 150000001299 aldehydes Chemical class 0.000 title claims abstract description 51
- 150000002576 ketones Chemical class 0.000 title claims abstract description 46
- 239000002253 acid Substances 0.000 title description 35
- -1 retention aids Substances 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- 239000002270 dispersing agent Substances 0.000 claims abstract description 10
- 230000014759 maintenance of location Effects 0.000 claims abstract description 8
- 239000002562 thickening agent Substances 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000000047 product Substances 0.000 abstract description 16
- 239000000654 additive Substances 0.000 abstract description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 84
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 58
- 239000000243 solution Substances 0.000 description 49
- 238000006243 chemical reaction Methods 0.000 description 34
- 239000007787 solid Substances 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 30
- 229940022682 acetone Drugs 0.000 description 28
- 150000001875 compounds Chemical class 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000004568 cement Substances 0.000 description 16
- 238000004519 manufacturing process Methods 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- 235000010265 sodium sulphite Nutrition 0.000 description 15
- 239000004567 concrete Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 13
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 12
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical class NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 11
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 9
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- 230000000694 effects Effects 0.000 description 8
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 7
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 7
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- 239000008098 formaldehyde solution Substances 0.000 description 7
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- 239000000126 substance Substances 0.000 description 7
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- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 6
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 6
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- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
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- 229960003080 taurine Drugs 0.000 description 4
- DSBZMUUPEHHYCY-UHFFFAOYSA-N 2-oxo-1,3,2-dioxathietan-4-one Chemical compound O=C1OS(=O)O1 DSBZMUUPEHHYCY-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 229930040373 Paraformaldehyde Natural products 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000005553 drilling Methods 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- YIBPLYRWHCQZEB-UHFFFAOYSA-N formaldehyde;propan-2-one Chemical compound O=C.CC(C)=O YIBPLYRWHCQZEB-UHFFFAOYSA-N 0.000 description 3
- JWIGFENOHPRSOM-UHFFFAOYSA-N formaldehyde;propan-2-one;sulfurous acid Chemical compound O=C.CC(C)=O.OS(O)=O JWIGFENOHPRSOM-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000003998 acyclic ketones Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
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- 125000003118 aryl group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
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- 238000005755 formation reaction Methods 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 2
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- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
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- 229960003868 paraldehyde Drugs 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- VSVCAMGKPRPGQR-UHFFFAOYSA-N propan-2-one;sulfurous acid Chemical compound CC(C)=O.OS(O)=O VSVCAMGKPRPGQR-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- 159000000000 sodium salts Chemical class 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
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- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
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- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
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- ACPXHHDRVABPNY-UHFFFAOYSA-N 4-acetylbenzenesulfonic acid Chemical compound CC(=O)C1=CC=C(S(O)(=O)=O)C=C1 ACPXHHDRVABPNY-UHFFFAOYSA-N 0.000 description 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical class NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 1
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- 239000010755 BS 2869 Class G Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241001319955 Unda Species 0.000 description 1
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- 238000002329 infrared spectrum Methods 0.000 description 1
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- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
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- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
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- YNJORDSKPXMABC-UHFFFAOYSA-M sodium;2-hydroxypropane-2-sulfonate Chemical compound [Na+].CC(C)(O)S([O-])(=O)=O YNJORDSKPXMABC-UHFFFAOYSA-M 0.000 description 1
- PUWCULQGLSPCMQ-UHFFFAOYSA-M sodium;4-acetylbenzenesulfonate Chemical compound [Na+].CC(=O)C1=CC=C(S([O-])(=O)=O)C=C1 PUWCULQGLSPCMQ-UHFFFAOYSA-M 0.000 description 1
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- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
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- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
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- 238000001966 tensiometry Methods 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/28—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/30—Condensation polymers of aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G6/00—Condensation polymers of aldehydes or ketones only
- C08G6/02—Condensation polymers of aldehydes or ketones only of aldehydes with ketones
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/14—Derivatives of phosphoric acid
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/584—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific surfactants
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/935—Enhanced oil recovery
- Y10S507/936—Flooding the formation
- Y10S507/937—Flooding the formation with emulsion
- Y10S507/938—Flooding the formation with emulsion with microemulsion
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Structural Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Chemical Treatment Of Metals (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Lubricants (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813144673 DE3144673A1 (de) | 1981-11-10 | 1981-11-10 | Saeuregruppen enthaltende thermostabile, hydrophile kondensationsprodukte von aldehyden und ketonen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD211354A5 true DD211354A5 (de) | 1984-07-11 |
Family
ID=6146063
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD82255303A DD211354A5 (de) | 1981-11-10 | 1982-11-09 | Verwendung von saeuregruppen enthaltenden thermostabilen, hydrophilen kondensationsprodukten von aldehyden und ketonen |
| DD82244692A DD208362A5 (de) | 1981-11-10 | 1982-11-09 | Verfahren zur herstellung von saeuregruppen enthaltenden thermostabilen, hydrophilen kondensationsprodukten |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD82244692A DD208362A5 (de) | 1981-11-10 | 1982-11-09 | Verfahren zur herstellung von saeuregruppen enthaltenden thermostabilen, hydrophilen kondensationsprodukten |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US4657593A (fi) |
| EP (1) | EP0078938B1 (fi) |
| JP (1) | JPS5887111A (fi) |
| KR (1) | KR890003001B1 (fi) |
| AT (1) | ATE31323T1 (fi) |
| AU (1) | AU543955B2 (fi) |
| BR (1) | BR8206501A (fi) |
| CA (1) | CA1188032A (fi) |
| CS (1) | CS244913B2 (fi) |
| DD (2) | DD211354A5 (fi) |
| DE (2) | DE3144673A1 (fi) |
| DK (1) | DK168541B1 (fi) |
| DZ (1) | DZ474A1 (fi) |
| EG (1) | EG15854A (fi) |
| ES (1) | ES8307850A1 (fi) |
| FI (1) | FI70585C (fi) |
| GR (1) | GR76717B (fi) |
| HU (1) | HU191364B (fi) |
| NO (1) | NO158544C (fi) |
| NZ (1) | NZ202287A (fi) |
| PL (1) | PL137954B1 (fi) |
| PT (1) | PT75711B (fi) |
| RO (1) | RO85635B (fi) |
| SG (1) | SG8088G (fi) |
| YU (1) | YU42814B (fi) |
| ZA (1) | ZA828041B (fi) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3344291A1 (de) * | 1983-12-07 | 1985-06-13 | Skw Trostberg Ag, 8223 Trostberg | Dispergiermittel fuer salzhaltige systeme |
| DE3410820A1 (de) * | 1984-03-23 | 1985-10-03 | Skw Trostberg Ag, 8223 Trostberg | Zusatzmittel fuer beton und zementmoertel mit verlaengerter wirkungsdauer |
| US4557763A (en) * | 1984-05-30 | 1985-12-10 | Halliburton Company | Dispersant and fluid loss additives for oil field cements |
| DE3429068A1 (de) * | 1984-08-07 | 1986-02-20 | Skw Trostberg Ag, 8223 Trostberg | Metallverbindungen von saeuregruppen enthaltenden kondensationsprodukten oder co-kondensationsprodukten von ketonen und aldehyden |
| ATE47707T1 (de) * | 1986-04-02 | 1989-11-15 | Sicotan Gmbh & Co Kg | Verfahren zum verfestigen von betonbauwerken und zum herstellen von moerteln, betonen oder hieraus bestehende produkte und ein hierfuer ausgebildeter zementleim. |
| DE3825530A1 (de) * | 1987-08-07 | 1989-02-16 | Sueddeutsche Kalkstickstoff | Retentionsmittel fuer waessrige systeme |
| US5089056A (en) * | 1989-04-21 | 1992-02-18 | Thiele Kaolin Company | Opacifying kaolin pigments and process for making same by reacting with sodium hydroxide in water |
| US5203629A (en) | 1990-08-07 | 1993-04-20 | W.R. Grace & Co.-Conn. | Method for modifying concrete properties |
| US5224774A (en) * | 1990-08-07 | 1993-07-06 | W. R. Grace & Co.-Conn. | Concrete additive product and method of use |
| US5320851A (en) * | 1992-01-31 | 1994-06-14 | W. R. Grace & Co.-Conn. | Packaging and dispensing system for fluid and semi-fluid cement admixtures |
| DE4217181A1 (de) * | 1992-05-23 | 1993-11-25 | Chemie Linz Deutschland | Verwendung von Kondensationsprodukten aus Melamin und Glyoxylsäure als Zusatzmittel für hydraulische Bindemittel und Baustoff |
| DE4227417C1 (de) * | 1992-08-19 | 1993-12-09 | Holderchem Betec Gmbh | Hydraulisch abbindendes Injektionsmaterial für ringförmige Spalträume großer Länge |
| US5290357A (en) * | 1992-12-22 | 1994-03-01 | Halliburton Company | Acetone/formaldehyde/cyanide resins |
| US5346012A (en) * | 1993-02-01 | 1994-09-13 | Halliburton Company | Fine particle size cement compositions and methods |
| US5358043A (en) * | 1993-03-22 | 1994-10-25 | Phillips Petroleum Company | Gelling compositions useful for oil field applications |
| US5355955A (en) * | 1993-07-02 | 1994-10-18 | Halliburton Company | Cement set retarding additives, compositions and methods |
| DE4325090C1 (de) * | 1993-07-27 | 1994-05-26 | Holderchem Betec Gmbh | Hydraulisch abbindendes Injektionsmaterial für ringförmige Spalträume großer Längen |
| DE4421715A1 (de) | 1994-06-21 | 1996-01-04 | Sueddeutsche Kalkstickstoff | Verwendung von Pfropfpolymeren auf Basis von Keton-Aldehyd-Kondensations- bzw. Co-Kondensationsprodukten |
| DE4434010C2 (de) * | 1994-09-23 | 2001-09-27 | Sueddeutsche Kalkstickstoff | Redispergierbare Polymerisatpulver, Verfahren zu deren Herstellung und Verwendung |
| US5697458A (en) * | 1996-05-02 | 1997-12-16 | Carney; Leroy Lloyd | Drilling fluid process |
| US5873936A (en) * | 1997-11-17 | 1999-02-23 | Maxxon Corp. | Cement composition self-leveling floor coating formulations and their method of use |
| WO2013143705A1 (en) | 2012-03-30 | 2013-10-03 | Technische Universität München | Concrete admixtures |
| EP2679613A1 (de) | 2012-06-26 | 2014-01-01 | Construction Research & Technology GmbH | Tonverträgliches Additiv für bauchemische Produkte |
| EP2848597A1 (en) | 2013-09-17 | 2015-03-18 | Basf Se | Light-weight gypsum board with improved strength and method for making same |
| US9359254B2 (en) | 2013-11-12 | 2016-06-07 | Baker Hughes Incorporated | Wellbore cement compositions and wellbore cementing methods |
| DE102014203231A1 (de) * | 2014-02-24 | 2015-08-27 | Evonik Degussa Gmbh | Dispergierharze für Pigmentpräparationen mit geringem flüchtigem organischem Anteil |
| US10221275B2 (en) | 2014-08-29 | 2019-03-05 | Sekisui Chemical Co., Ltd. | Furan resin, method for producing same, thermosetting furan resin composition, cured product, and furan resin composite |
| JP6429181B2 (ja) * | 2014-09-11 | 2018-11-28 | 花王株式会社 | 縮合物の製造方法 |
| WO2018091659A1 (en) | 2016-11-21 | 2018-05-24 | Basf Se | Composition for inorganic binders |
| CA3117346A1 (en) | 2018-10-31 | 2020-05-07 | Basf Se | Enhanced dewatering of mining tailings employing chemical pre-treatment |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US841999A (en) * | 1906-03-20 | 1907-01-22 | Hoechst Ag | Process of making formaldehyde sulfoxylates. |
| US2174127A (en) * | 1937-12-13 | 1939-09-26 | Du Pont | Sulphated acyloins and process of producing them |
| US2432850A (en) * | 1941-05-02 | 1947-12-16 | Chem Ind Basel | Water-soluble condensation products and process of making same |
| US2641591A (en) * | 1949-05-12 | 1953-06-09 | Dan River Mills Inc | Method of manufacturing acetoneformaldehyde condensation products |
| CH303271A (de) * | 1949-10-14 | 1954-11-30 | Forestal Land Timber & Railway | Verfahren zur Herstellung harzartiger, wasserlöslicher Kondensationsprodukte aus Formaldehyd und Aceton. |
| US2857433A (en) * | 1956-06-20 | 1958-10-21 | Olin Mathieson | Aromatic ketones and process of their production |
| US3149152A (en) * | 1961-01-03 | 1964-09-15 | Ethicon Inc | Mono-alkali metal bisulfites of dialdehydes |
| DE1720729A1 (de) * | 1967-10-17 | 1971-07-08 | Bayer Ag | Kondensationsprodukte |
| FR1568994A (fi) * | 1968-03-19 | 1969-05-30 | ||
| US3956140A (en) * | 1970-08-03 | 1976-05-11 | Dresser Industries, Inc. | Drilling fluids |
| JPS5610327B2 (fi) * | 1973-06-04 | 1981-03-07 | ||
| DE2542090C2 (de) * | 1975-09-20 | 1983-08-25 | Bayer Ag, 5090 Leverkusen | Kondensationsprodukte aus Cycloalkanonen, Formaldehyd und Alkalibisulfit |
| FR2415084A1 (fr) * | 1978-01-20 | 1979-08-17 | Protex Manuf Prod Chimiq | Compositions additives pour melanges a base de ciments hydrauliques |
| DE2831613C2 (de) * | 1978-07-19 | 1982-03-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Polykondensationsprodukten |
-
1981
- 1981-11-10 DE DE19813144673 patent/DE3144673A1/de not_active Ceased
-
1982
- 1982-10-07 DZ DZ826704A patent/DZ474A1/fr active
- 1982-10-14 GR GR69543A patent/GR76717B/el unknown
- 1982-10-15 AT AT82109565T patent/ATE31323T1/de not_active IP Right Cessation
- 1982-10-15 DE DE8282109565T patent/DE3277820D1/de not_active Expired
- 1982-10-15 EP EP82109565A patent/EP0078938B1/de not_active Expired
- 1982-10-21 PT PT75711A patent/PT75711B/pt not_active IP Right Cessation
- 1982-10-26 NZ NZ202287A patent/NZ202287A/en unknown
- 1982-10-27 CS CS827650A patent/CS244913B2/cs unknown
- 1982-10-28 CA CA000414356A patent/CA1188032A/en not_active Expired
- 1982-11-01 EG EG650/82A patent/EG15854A/xx active
- 1982-11-03 ZA ZA828041A patent/ZA828041B/xx unknown
- 1982-11-08 RO RO108993A patent/RO85635B/ro unknown
- 1982-11-08 YU YU2500/82A patent/YU42814B/xx unknown
- 1982-11-09 HU HU823599A patent/HU191364B/hu not_active IP Right Cessation
- 1982-11-09 NO NO823733A patent/NO158544C/no not_active IP Right Cessation
- 1982-11-09 KR KR8205062A patent/KR890003001B1/ko active
- 1982-11-09 BR BR8206501A patent/BR8206501A/pt unknown
- 1982-11-09 DD DD82255303A patent/DD211354A5/de not_active IP Right Cessation
- 1982-11-09 FI FI823840A patent/FI70585C/fi not_active IP Right Cessation
- 1982-11-09 DK DK499182A patent/DK168541B1/da not_active IP Right Cessation
- 1982-11-09 PL PL1982238945A patent/PL137954B1/pl unknown
- 1982-11-09 AU AU90271/82A patent/AU543955B2/en not_active Expired
- 1982-11-09 DD DD82244692A patent/DD208362A5/de not_active IP Right Cessation
- 1982-11-10 JP JP57196163A patent/JPS5887111A/ja active Granted
- 1982-11-10 ES ES517264A patent/ES8307850A1/es not_active Expired
-
1985
- 1985-07-15 US US06/755,224 patent/US4657593A/en not_active Expired - Lifetime
-
1988
- 1988-02-02 SG SG80/88A patent/SG8088G/en unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |