EP0165252A4 - Composition modifiee de diamine d'alcene ou de polyamine de polyalcene et pate de ciment hydraulique aqueuse utilisant cette composition. - Google Patents
Composition modifiee de diamine d'alcene ou de polyamine de polyalcene et pate de ciment hydraulique aqueuse utilisant cette composition.Info
- Publication number
- EP0165252A4 EP0165252A4 EP19840903921 EP84903921A EP0165252A4 EP 0165252 A4 EP0165252 A4 EP 0165252A4 EP 19840903921 EP19840903921 EP 19840903921 EP 84903921 A EP84903921 A EP 84903921A EP 0165252 A4 EP0165252 A4 EP 0165252A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- average molecular
- molecular weight
- mixture
- polyalkylenepolyamine
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 79
- 239000002002 slurry Substances 0.000 title claims abstract description 20
- 125000005263 alkylenediamine group Chemical group 0.000 title claims abstract description 15
- 239000011396 hydraulic cement Substances 0.000 title claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229920000768 polyamine Polymers 0.000 claims description 20
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 239000000654 additive Substances 0.000 claims description 14
- 239000004568 cement Substances 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 230000000996 additive effect Effects 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 238000012360 testing method Methods 0.000 claims description 8
- 239000008186 active pharmaceutical agent Substances 0.000 claims description 6
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000012530 fluid Substances 0.000 claims description 2
- 239000011149 active material Substances 0.000 claims 6
- 239000002245 particle Substances 0.000 abstract description 3
- 239000012736 aqueous medium Substances 0.000 abstract description 2
- 239000010808 liquid waste Substances 0.000 abstract description 2
- 238000005065 mining Methods 0.000 abstract description 2
- 238000000746 purification Methods 0.000 abstract description 2
- 239000007787 solid Substances 0.000 abstract description 2
- 238000005189 flocculation Methods 0.000 abstract 1
- 230000016615 flocculation Effects 0.000 abstract 1
- 239000000047 product Substances 0.000 description 15
- 239000000243 solution Substances 0.000 description 12
- 239000000499 gel Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 239000004971 Cross linker Substances 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229940063013 borate ion Drugs 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229920006037 cross link polymer Polymers 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Chemical group 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- C04B24/12—Nitrogen containing compounds organic derivatives of hydrazine
- C04B24/121—Amines, polyamines
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C08G73/022—Preparatory process from polyamines and epihalohydrins
Definitions
- the present invention resides in a modified alkylenediamine or polyalkylenepolyamine composition.
- the composition is suitable for use as a fluid loss additive in aqueous hydraulic cement slurry compositions or as a floccuiant for water purification, liquid waste treatment, or in the mining industry where such flocculants are added to suspension of solid particles (fines) in water or other aqueous media (pulps) to cause the individual particles to collect in the form of blocks.
- Hydraulic cements i.e., any inorganic cement that hardens or sets under water, are customarily admixed with water and emplaced as aqueous slurries.
- the amount of water employed may vary rather extensively depending largely upon the fluidity of the slurry required and upon the necessary ultimate strength.
- a hydraulic cement it is necessary for the cement slurry to be emplaced within or next to a porous medium, for example, earthen strata, e.g., in the cementing off of boreholes, grouting, dam and tunnel construction and the like. When such is the case, water filters out of the slurry and into the strata during the setting period.
- One such material comprises a polyamine compound selected from the polyalkyleneimines, polyalkylenepolyamines or mixtures thereof. A description of these polyamine compounds and their use in hydraulic cement slurries is taught, for example, in U.S. Patent No. 3,491,049.
- the composition of the present invention is advantageously employed as a fluid loss additive in a cement slurry and is more efficient, i.e. it requires less of the active additives to achieve the same level of water loss or, at the same level of active additives, less water loss occurs while also providing more stable, non-settling, cement slurries.
- the present invention particularly resides in a modified alkylenediamine or polyalkylenepolyamine composition comprising the product resulting from reacting a modified alkylenediamine or polyalkylenepolyamine composition, characterized in that the composition is the reaction product resulting from reacting
- composition prepared by reacting (a) a polyalkylenepolyamine composition having an average molecular weight of from 60 to 500 with (b) at least one alkylene dihalide; wherein component (A-2-a) and component (A-2-b) are reacted in quantities such that the quantity of (A-2-b) used is less than the amount needed to form a gel by an amount
- (C) optionally, one or more adducts of (1) at least one epihalohydrin, dihalohydrin or mixture thereof; and (2) at least one alkylenediamine or polyalkylenepolyamine having an average molecular weight of from 60 to 500 or a mixture thereof; and wherein components (A), (B) and (C) are employed in quantities which provide a non-gelled polyamine which given a fluid loss of less than about 60 ml according to the API RP 10B fluid loss test described in the examples.
- the invention also resides in an aqueous hydraulic cement slurry composition
- aqueous hydraulic cement slurry composition comprising water, hydraulic cement, surfactant and polyalkylenepolyamine fluid loss additive; characterized by employing as said fluid loss additive, at least one composition prepared by reacting
- component (a) a polyalkylenepolyamine composition having an average molecular weight of from 60 to 500 with (b) at least one alkylene dihalide; wherein component (A-2-a) and component (A-2-b) are reacted in quantities such that the quantity of (A-2-b) used is less than the amount needed to form a gel by an amount (expressed as weight of carbon and hydrogen contained in (A-2-b) of from 0.8% to 5% of the weight of carbon plus hydrogen plus nitrogen present in the reaction mixture when a gel would be formed; (3) mixtures of (1) and (2); with (B) at least one of
- a series of lab scale reactions are employed with varying ratios of reactants of alkylene dichloride:polyalkylenepolyamine such as, for example, 0.4:1, 0.5:1, 0.6:1, 0.8:1 and 1.1:1 by weight are conducted at a suitable temperature and water concentration. From the lowest ratio that created the gel new proportions are selected in the following manner, assuming a ratio of 0.55:1 produced a gel. Assuming that the following arbitrary formulation produces a gel ( in grams).
- the amount of carbon plus hydrogen to leave out of the recipe is from 19 g to 115 g which corresponds to 67 to 406 grams of EDC.
- the amount of crosslinking agent to be further added is determined by adding small portions of crosslinking agent to about 100 grams of the first product until the product gels. At that point (assume 6 grams of 50% active crosslinking agent produced the gel) a series of samples are prepared using 6 g/100 g, 5 g/100 g, 4 g/100 g, etc. The ratio which gives a product with a viscosity of from 1000 to 4000, preferably from 2000 to 3000, cps is the one which would be used to complete the reaction.
- Suitable alkylenediamines and polyalkylenepolyamines which can be employed herein include polyethylenepolyamines having an average molecular weight of from 60 to 500, preferably from 150 to 350, which can be prepared by reacting a vicinal alkylene dihalide having from 2 to 6 carbon atoms with ammonia or lower alkyleneamines such as, for example, ethylenediamine, diethylenetriamine and the like.
- Suitable methods of preparation are disclosed by Garms et al in U.S. Patent No. 3,210,308.
- Particularly suitable are the bottoms product from the preparation of ethylenediamine from ammonia and ethylene dichloride.
- bottoms product it is meant that which results after substantially removing those compounds boiling lower than pentaethylenehexamine from the reaction product resulting from reacting ammonia with ethylene dichloride.
- Suitable epihalohydrins and/or dihalohydrins which can be employed herein include those represented by the formulas
- each R is hydrogen or an alkyl group having from 1 to 4 carbon atoms and each X is independently chlorine or bromine.
- the cement slurry also contains an effective amount of a surfactant such as, for example, a water dispersable lignosulfate, lignoamine, sulfonic acids, mixtures thereof and the like.
- a surfactant such as, for example, a water dispersable lignosulfate, lignoamine, sulfonic acids, mixtures thereof and the like.
- An amount of from 0.25 to 5 parts by weight is preferred.
- An amount of from 0.5 to 1.5 parts by weight is most preferred.
- cement slurry compositions may also contain a borate ion releasing compound and/or a carbonate and/or a bicarbonate as disclosed by Crinkelmeyer et al in U.S. Patent No. 4,131,578.
- the quantities of components of the aqueous cement slurry composition of the present invention are based on 100 parts by weight of hydraulic cement as follows:
- Fluid Loss Additive 0.5 to 8, preferably 0.75 to 3 Surfactant --- 0.25 to 5, preferably 0.5 to 1.5
- Carbonate of Bicarbonate 0 to 3 preferably
- active not all of the product is regarded as "active".
- the active portion of the product is the carbon + nitrogen + hydrogen portion of the aqueous solutions produced. Percent active is calculated as the weight of (carbon + nitrogen + hydrogen) divided by the total weight of the amine solution multiplied by 100.
- API RP 10B using a Baroid high temperature high pressure fluid loss apparatus and a 325 mesh (U.S.
- Standard Sieve Series stainless steel screen. 100 parts by weight Lone Star type H cement was mixed with
- a surfactant material which is the condensation product of formaldehyde and mononaphthalenesulfonic acid. 42 parts by weight of water was mixed with the desired amount of the active polyamine (1.1% by weight of the cement employed). The water and cement were then blended together and digested at 200°F (93.3°C) for 20 minutes. The slurry was added to the filtration cell which was preheated to 200°F (93.3oC) and the fluid loss (in cm 3 /30 min) was measured with 1000 psig (6.89 kPa) nitrogen pressure on the filtration cell. The fluid loss measure was then multiplied by 2 so as to adjust for the size of the screen used with the filtration cell.
- Example 1-A To 300 g of polyalkylenepolyamine prepared in Example 1-A was added 8 g of epichlorohydrin. The mixture was reacted at a temperature of 60°C in a shaker bath overnight. An amber solution was produced. This material was tested according to Example 1-D. The results are given in Table I.
- Example 4 was repeated employing 1200 g of Polyamine 300 and 618 g of ethylene dichloride. The resultant viscosity was >6000 cps. The product was tested as a fluid loss additive employing the procedure of Example 1-D. The results are given in Table I.
- EXAMPLE 7 1683 g water and 886 g of polyamine 300 were mixed in a 5-liter flask. A mixture of 380 g ethylenedichloride (EDC) and 51.2 g of epichlorohydrin (EPI) was added slowly over 4.5 hours to the amine-water solution. The temperature of the reaction was maintained at a temperature of from 65 to 70°C. 17.5 g of a cross-linker prepared as in Example 2A was added to 150 g of the polyamide-EDC-EPI product. The mixture was reacted at 100°C for 30 minutes. The resulting polymer solution had a viscosity >300 cps and was tested as a fluid loss additive (1.2% based on cement). The results are given in Table 1.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US548475 | 1983-11-03 | ||
| US06/548,475 US4461856A (en) | 1983-11-03 | 1983-11-03 | Aqueous hydraulic cement slurry |
| US06/586,374 US4482667A (en) | 1983-11-03 | 1984-03-05 | Modified polyalkylenepolyamines |
| US586374 | 1984-03-05 | ||
| US638824 | 1984-08-08 | ||
| US06/638,824 US4519843A (en) | 1983-11-03 | 1984-08-08 | Modified polyalkylenepolyamines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0165252A1 EP0165252A1 (fr) | 1985-12-27 |
| EP0165252A4 true EP0165252A4 (fr) | 1986-07-23 |
Family
ID=27415533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19840903921 Withdrawn EP0165252A4 (fr) | 1983-11-03 | 1984-10-29 | Composition modifiee de diamine d'alcene ou de polyamine de polyalcene et pate de ciment hydraulique aqueuse utilisant cette composition. |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0165252A4 (fr) |
| BR (1) | BR8407149A (fr) |
| CA (1) | CA1217205A (fr) |
| IT (1) | IT1177106B (fr) |
| NO (1) | NO852648L (fr) |
| WO (1) | WO1985001935A1 (fr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3809964C2 (de) * | 1987-03-24 | 1994-08-25 | Nippon Catalytic Chem Ind | Zement-Dispergiermittel, Verfahren zu seiner Herstellung und seine Verwendung |
| US4892589A (en) * | 1987-10-30 | 1990-01-09 | Aqualon Company | Composition comprising water-soluble, nonionic hydrophobically modified hydroxyethyl cellulose and water-soluble, nonionic hydroxyethyl cellulose |
| FR2887541B1 (fr) * | 2004-09-21 | 2007-10-12 | Lafarge Sa | Compositions d'inertage d'impuretes |
| ATE532756T1 (de) | 2004-09-21 | 2011-11-15 | Lafarge Sa | Verfahren zur inertisierung von unreinheiten |
| WO2006032786A2 (fr) * | 2004-09-21 | 2006-03-30 | Lafarge | Compositions d'inertage d'impuretes |
| AU2012370954B2 (en) | 2012-02-22 | 2016-08-11 | Gcp Applied Technologies Inc. | Functionalized polyamines for clay mitigation |
| ES2596438T3 (es) | 2012-05-04 | 2017-01-09 | Gcp Applied Technologies Inc. | Método para tratar arcilla y agregados arcillosos y composiciones destinadas a ello |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3210308A (en) * | 1962-07-06 | 1965-10-05 | Dow Chemical Co | Polymeric flocculants |
| US3247048A (en) * | 1962-09-10 | 1966-04-19 | Monsanto Co | Nitrogen prepolymers as wet and dry strength improvers for paper |
| CH451513A (de) * | 1965-03-26 | 1968-05-15 | Ciba Geigy | Verfahren zur Herstellung von neuen härtbaren stickstoffhaltigen Kondensationsprodukten |
| US3491049A (en) * | 1965-10-13 | 1970-01-20 | Dow Chemical Co | Low water-loss aqueous cement slurry and method of use |
| US3511314A (en) * | 1968-10-28 | 1970-05-12 | Dow Chemical Co | Cementing composition and well cementing process employing same |
| US4131578A (en) * | 1975-02-03 | 1978-12-26 | The Dow Chemical Company | Aqueous hydraulic cement slurry |
| US3988279A (en) * | 1975-04-23 | 1976-10-26 | Celanese Coatings & Specialties Company | Thermosetting concrete-containing epoxy |
| US4129528A (en) * | 1976-05-11 | 1978-12-12 | Monsanto Company | Polyamine-epihalohydrin resinous reaction products |
| US4260700A (en) * | 1977-01-24 | 1981-04-07 | The B.F. Goodrich Company | Underwater curing of epoxy resin and amine-terminated liquid polymer and product thereof |
| US4191820A (en) * | 1978-01-03 | 1980-03-04 | Basf Wyandotte Corporation | Process for preparing polyalkylene polyamine polyethers |
| DE3003648A1 (de) * | 1980-02-01 | 1981-08-06 | Basf Ag, 6700 Ludwigshafen | Verfahren zur zerstellung von wasserloeslichen, stickstoffhaltigen kondensationsprodukten und deren verwendung bei der papierherstellung |
| US4316003A (en) * | 1980-10-23 | 1982-02-16 | Shell Oil Company | Epoxy resin curing agents |
-
1984
- 1984-10-29 CA CA000466497A patent/CA1217205A/fr not_active Expired
- 1984-10-29 BR BR8407149A patent/BR8407149A/pt unknown
- 1984-10-29 WO PCT/US1984/001743 patent/WO1985001935A1/fr not_active Ceased
- 1984-10-29 EP EP19840903921 patent/EP0165252A4/fr not_active Withdrawn
- 1984-11-02 IT IT23439/84A patent/IT1177106B/it active
-
1985
- 1985-07-02 NO NO852648A patent/NO852648L/no unknown
Non-Patent Citations (2)
| Title |
|---|
| No relevant documents have been disclosed * |
| See also references of WO8501935A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| NO852648L (no) | 1985-07-02 |
| IT8423439A1 (it) | 1986-05-02 |
| IT1177106B (it) | 1987-08-26 |
| WO1985001935A1 (fr) | 1985-05-09 |
| CA1217205A (fr) | 1987-01-27 |
| EP0165252A1 (fr) | 1985-12-27 |
| IT8423439A0 (it) | 1984-11-02 |
| BR8407149A (pt) | 1985-10-08 |
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