CA1228080A - Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment - Google Patents

Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment

Info

Publication number: CA1228080A
Authority: CA; Canada
Prior art keywords: cement; iii; formula; salts; carbon atoms
Prior art date: 1984-06-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000457393A

Other languages

English (en)

Inventor

Druce K. Crump

David A. Wilson

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Chemical Co

Original Assignee

Dow Chemical Co

Priority date (The priority date 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 date listed.)

1984-06-26

Filing date

1984-06-26

Publication date

1987-10-13

1984-06-26 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1984-06-26 Priority to CA000457393A priority Critical patent/CA1228080A/fr

1987-10-13 Application granted granted Critical

1987-10-13 Publication of CA1228080A publication Critical patent/CA1228080A/fr

Status Expired legal-status Critical Current

Links

239000004568 cement Substances 0.000 title claims abstract description 24
239000002253 acid Substances 0.000 title claims abstract description 18
230000000979 retarding effect Effects 0.000 title claims abstract description 7
239000000654 additive Substances 0.000 title abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 14
150000003839 salts Chemical class 0.000 claims abstract description 12
-1 trialkylammonium halide Chemical class 0.000 claims abstract description 9
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
239000001257 hydrogen Substances 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 4
125000000217 alkyl group Chemical group 0.000 claims abstract description 3
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 3
238000000034 method Methods 0.000 claims description 9
239000002002 slurry Substances 0.000 claims description 5
229910052783 alkali metal Inorganic materials 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims description 4
229920000768 polyamine Polymers 0.000 claims description 2
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 2
150000001340 alkali metals Chemical class 0.000 claims 1
229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
159000000000 sodium salts Chemical class 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
239000011398 Portland cement Substances 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
229940116254 phosphonic acid Drugs 0.000 description 6
238000010992 reflux Methods 0.000 description 6
239000000047 product Substances 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
229960000443 hydrochloric acid Drugs 0.000 description 4
235000011167 hydrochloric acid Nutrition 0.000 description 4
239000000243 solution Substances 0.000 description 4
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 4
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
239000004148 curcumin Substances 0.000 description 3
UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 3
239000008098 formaldehyde solution Substances 0.000 description 3
239000003129 oil well Substances 0.000 description 3
230000008719 thickening Effects 0.000 description 3
LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 description 3
VFKZECOCJCGZQK-UHFFFAOYSA-M 3-hydroxypropyl(trimethyl)azanium;chloride Chemical group [Cl-].C[N+](C)(C)CCCO VFKZECOCJCGZQK-UHFFFAOYSA-M 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
239000004606 Fillers/Extenders Substances 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000010440 gypsum Substances 0.000 description 2
229910052602 gypsum Inorganic materials 0.000 description 2
239000013067 intermediate product Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
239000002994 raw material Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
RUUHDEGJEGHQKL-UHFFFAOYSA-M 2-hydroxypropyl(trimethyl)azanium;chloride Chemical group [Cl-].CC(O)C[N+](C)(C)C RUUHDEGJEGHQKL-UHFFFAOYSA-M 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229910001570 bauxite Inorganic materials 0.000 description 1
238000001354 calcination Methods 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052681 coesite Inorganic materials 0.000 description 1
229910052593 corundum Inorganic materials 0.000 description 1
229910052906 cristobalite Inorganic materials 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
HOOWDPSAHIOHCC-UHFFFAOYSA-N dialuminum tricalcium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[Al+3].[Al+3].[Ca++].[Ca++].[Ca++] HOOWDPSAHIOHCC-UHFFFAOYSA-N 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
BCAARMUWIRURQS-UHFFFAOYSA-N dicalcium;oxocalcium;silicate Chemical compound [Ca+2].[Ca+2].[Ca]=O.[O-][Si]([O-])([O-])[O-] BCAARMUWIRURQS-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000036571 hydration Effects 0.000 description 1
238000006703 hydration reaction Methods 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical class [H]O* 0.000 description 1
239000000411 inducer Substances 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000000463 material 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
125000005461 organic phosphorous group Chemical group 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000005086 pumping Methods 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000002893 slag Substances 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000002277 temperature effect Effects 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
229910021534 tricalcium silicate Inorganic materials 0.000 description 1
235000019976 tricalcium silicate Nutrition 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
229910001845 yogo sapphire Inorganic materials 0.000 description 1
229910000859 α-Fe Inorganic materials 0.000 description 1

Landscapes

Curing Cements, Concrete, And Artificial Stone (AREA)

CA000457393A 1984-06-26 1984-06-26 Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment Expired CA1228080A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000457393A CA1228080A (fr)	1984-06-26	1984-06-26	Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000457393A CA1228080A (fr)	1984-06-26	1984-06-26	Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment

Publications (1)

Publication Number	Publication Date
CA1228080A true CA1228080A (fr)	1987-10-13

Family

ID=4128172

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000457393A Expired CA1228080A (fr)	1984-06-26	1984-06-26	Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment

Country Status (1)

Country	Link
CA (1)	CA1228080A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN114685797A (zh) *	2020-12-31	2022-07-01	南京博特新材料有限公司	一种含羧基和膦酸基的减水剂及其制备方法

1984
- 1984-06-26 CA CA000457393A patent/CA1228080A/fr not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN114685797A (zh) *	2020-12-31	2022-07-01	南京博特新材料有限公司	一种含羧基和膦酸基的减水剂及其制备方法
CN114685797B (zh) *	2020-12-31	2023-08-08	南京博特新材料有限公司	一种含羧基和膦酸基的减水剂及其制备方法

Legal Events

Date	Code	Title	Description
2004-10-13	MKEX	Expiry

Publication	Publication Date	Title
EP0166798A1 (fr)	1986-01-08	Réducteurs de prise comme ajouts à ciment à partir des dérivés de l'acide aminométhylènephosphorique
US4468252A (en)	1984-08-28	Set retarding additives for cement from aminomethylenephosphonic acid derivatives
US5879445A (en)	1999-03-09	Thinners for aqueous suspensions of mineral particles and hydraulic binder pastes
US4472200A (en)	1984-09-18	New additives for retarding setting of cement from methylenephosphonated aminohydrocarbylpiperazine-urea adducts
JPS6126540A (ja)	1986-02-05	アミノメチレンホスホン酸誘導体から成るセメント固定化遅延添加剤
EP0415799A2 (fr)	1991-03-06	Compositions améliorées de ciment mixte et de ciment portland
US4500356A (en)	1985-02-19	Methylenephosphonic acid derivatives of bis(aminoalkyl)piperazines as cement set retarding agents
EP1060147B1 (fr)	2001-10-31	Systemes retardateurs et application a la cimentation de puits de petrole
EP0166797A1 (fr)	1986-01-08	Compositions de ciment qui contiennent des rétardateurs de prise
EP0172950B1 (fr)	1988-03-30	Dérivés polymériques de pipérazine et d'acide alkylène phosphorique utilisés comme agents inhibiteurs de tartre
US3657134A (en)	1972-04-18	Deflocculation of solid materials in aqueous medium
CA1228080A (fr)	1987-10-13	Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment
JPS6126539A (ja)	1986-02-05	ジシクロペンタジエン誘導体を基材とする固定化遅延剤を含有するセメント組成物
EP0154474B1 (fr)	1988-11-09	Dérivés de bis(aminoalkyl)pipérazine et leur utilisation comme agents de contrôle des ions métalliques et comme agents retardateurs de la prise en masse du ciment
GB2157279A (en)	1985-10-23	Well treating composition
US4102701A (en)	1978-07-25	Plaster compositions containing oxo-polycarboxylic acids as a set retarder
CA1234582A (fr)	1988-03-29	Composition de ciment contenant des retardateurs de prise
EP0166020B1 (fr)	1991-04-17	Agents pour la chélation à base de dérivés de dicyclopentadiène
CA1223280A (fr)	1987-06-23	Agents retardateurs de prise pour ciments hydrauliques
EP1686101B1 (fr)	2008-05-07	Retardateur pour ciment
EP0172282A1 (fr)	1986-02-26	Utilisation des dérivés polymères de pipérazine d'acide phosphorique alkylène comme composés retardateurs de la prise de boues cimenteuses
US4540508A (en)	1985-09-10	Alkylene phosphonic acid scale inhibitor compositions
WO1986001194A1 (fr)	1986-02-27	Derives polymeres de piperazine de l'acide alkylenephosphorique utilises en tant que composes retardateurs de prise destines a etre utilises dans des boues de ciment
NO842635L (no)	1985-12-30	Fremgangsmaate til aa retardere stivningen av vandige sementvellinger.
CA1216742A (fr)	1987-01-20	Methode et composition de traitement de forages