CA1223280A - Agents retardateurs de prise pour ciments hydrauliques - Google Patents

Agents retardateurs de prise pour ciments hydrauliques

Info

Publication number: CA1223280A
Authority: CA; Canada
Prior art keywords: compound; cement; organic; hydrogen; dihalo
Prior art date: 1984-08-20
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

CA000461339A

Other languages

English (en)

Inventor

David A. Wilson

Druce K. Drump

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.)

1984-08-20

Filing date

1984-08-20

Publication date

1987-06-23

1984-08-20 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1984-08-20 Priority to CA000461339A priority Critical patent/CA1223280A/fr

1987-06-23 Application granted granted Critical

1987-06-23 Publication of CA1223280A publication Critical patent/CA1223280A/fr

Status Expired legal-status Critical Current

Links

239000004568 cement Substances 0.000 title claims abstract description 26
150000001875 compounds Chemical class 0.000 title claims description 16
239000002002 slurry Substances 0.000 title claims description 9
230000000979 retarding effect Effects 0.000 title claims description 8
-1 -halo compound Chemical class 0.000 claims abstract description 15
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims abstract description 7
239000007795 chemical reaction product Substances 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 10
238000000034 method Methods 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
150000003254 radicals Chemical class 0.000 claims description 5
229910052783 alkali metal Inorganic materials 0.000 claims description 4
150000002894 organic compounds Chemical class 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 4
239000000047 product Substances 0.000 abstract description 6
229920000642 polymer Polymers 0.000 abstract description 5
239000000654 additive Substances 0.000 description 14
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 9
239000011398 Portland cement Substances 0.000 description 7
230000000996 additive effect Effects 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000000203 mixture Substances 0.000 description 6
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 6
239000004593 Epoxy Substances 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
BHELIUBJHYAEDK-OAIUPTLZSA-N Aspoxicillin Chemical compound C1([C@H](C(=O)N[C@@H]2C(N3[C@H](C(C)(C)S[C@@H]32)C(O)=O)=O)NC(=O)[C@H](N)CC(=O)NC)=CC=C(O)C=C1 BHELIUBJHYAEDK-OAIUPTLZSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
235000009434 Actinidia chinensis Nutrition 0.000 description 3
244000298697 Actinidia deliciosa Species 0.000 description 3
235000009436 Actinidia deliciosa Nutrition 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical class C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
235000018936 Vitellaria paradoxa Nutrition 0.000 description 3
229920000180 alkyd Polymers 0.000 description 3
239000003129 oil well Substances 0.000 description 3
150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
230000011514 reflex Effects 0.000 description 3
WLOHKZPZHBMVBK-UHFFFAOYSA-N 2-(chloromethyl)oxirane Chemical compound ClCC1CO1.ClCC1CO1 WLOHKZPZHBMVBK-UHFFFAOYSA-N 0.000 description 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
239000002738 chelating agent Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
239000010440 gypsum Substances 0.000 description 2
229910052602 gypsum Inorganic materials 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000007788 liquid Substances 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
239000002994 raw material Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000000243 solution Substances 0.000 description 2
230000008719 thickening Effects 0.000 description 2
CZWSZZHGSNZRMW-UHFFFAOYSA-N 1,2-dibromobutane Chemical compound CCC(Br)CBr CZWSZZHGSNZRMW-UHFFFAOYSA-N 0.000 description 1
KFUSEUYYWQURPO-UHFFFAOYSA-N 1,2-dichloroethene Chemical compound ClC=CCl KFUSEUYYWQURPO-UHFFFAOYSA-N 0.000 description 1
YHRUOJUYPBUZOS-UHFFFAOYSA-N 1,3-dichloropropane Chemical compound ClCCCCl YHRUOJUYPBUZOS-UHFFFAOYSA-N 0.000 description 1
MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
YZNQITSGDRCUKE-UHFFFAOYSA-N 1-chloropropane Chemical compound [CH2]CCCl YZNQITSGDRCUKE-UHFFFAOYSA-N 0.000 description 1
FGRBYDKOBBBPOI-UHFFFAOYSA-N 10,10-dioxo-2-[4-(N-phenylanilino)phenyl]thioxanthen-9-one Chemical compound O=C1c2ccccc2S(=O)(=O)c2ccc(cc12)-c1ccc(cc1)N(c1ccccc1)c1ccccc1 FGRBYDKOBBBPOI-UHFFFAOYSA-N 0.000 description 1
DDLQNHHSWYGUDU-UHFFFAOYSA-N 2-(2-chloroethyl)-3-methyloxirane Chemical compound CC1OC1CCCl DDLQNHHSWYGUDU-UHFFFAOYSA-N 0.000 description 1
LSOXTBBDZHIHDE-UHFFFAOYSA-N 2-(3-chloropropyl)oxirane Chemical compound ClCCCC1CO1 LSOXTBBDZHIHDE-UHFFFAOYSA-N 0.000 description 1
MMTOSBCMFDNOIY-UHFFFAOYSA-N 2-(chloromethyl)-3-methyloxirane Chemical compound CC1OC1CCl MMTOSBCMFDNOIY-UHFFFAOYSA-N 0.000 description 1
KKZUMAMOMRDVKA-UHFFFAOYSA-N 2-chloropropane Chemical compound [CH2]C(C)Cl KKZUMAMOMRDVKA-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
239000004970 Chain extender Substances 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
244000007853 Sarothamnus scoparius Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
229910001570 bauxite Inorganic materials 0.000 description 1
HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
238000001354 calcination Methods 0.000 description 1
JHLNERQLKQQLRZ-UHFFFAOYSA-N calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
235000012241 calcium silicate Nutrition 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 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
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000011396 hydraulic cement Substances 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 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
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000005461 organic phosphorous group Chemical group 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000005086 pumping Methods 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000377 silicon dioxide Substances 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
239000000126 substance Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
229940066771 systemic antihistamines piperazine derivative Drugs 0.000 description 1
230000002277 temperature effect Effects 0.000 description 1
238000010998 test method Methods 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
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
229910000859 α-Fe Inorganic materials 0.000 description 1

Landscapes

Epoxy Resins (AREA)

CA000461339A 1984-08-20 1984-08-20 Agents retardateurs de prise pour ciments hydrauliques Expired CA1223280A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000461339A CA1223280A (fr)	1984-08-20	1984-08-20	Agents retardateurs de prise pour ciments hydrauliques

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000461339A CA1223280A (fr)	1984-08-20	1984-08-20	Agents retardateurs de prise pour ciments hydrauliques

Publications (1)

Publication Number	Publication Date
CA1223280A true CA1223280A (fr)	1987-06-23

Family

ID=4128553

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000461339A Expired CA1223280A (fr)	1984-08-20	1984-08-20	Agents retardateurs de prise pour ciments hydrauliques

Country Status (1)

Country	Link
CA (1)	CA1223280A (fr)

1984
- 1984-08-20 CA CA000461339A patent/CA1223280A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2004-08-20	MKEX	Expiry

Publication	Publication Date	Title
US4466836A (en)	1984-08-21	Set retarding compounds for use in cement slurries
EP0136790B1 (fr)	1988-10-19	Nouveaux additifs pour retarder la prise du ciment de produits d'addition méthylènephosphonaté d'aminohydrocarbylpipérazine-urée
US4468252A (en)	1984-08-28	Set retarding additives for cement from aminomethylenephosphonic acid derivatives
NO314723B1 (no)	2003-05-12	Anvendelse av fluidiseringsmidler for vandige suspensjoner av mineralpartikler og hydrauliske bindemiddelpastaer, samt nye forbindelser
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
EP0172950B1 (fr)	1988-03-30	Dérivés polymériques de pipérazine et d'acide alkylène phosphorique utilisés comme agents inhibiteurs de tartre
US4500356A (en)	1985-02-19	Methylenephosphonic acid derivatives of bis(aminoalkyl)piperazines as cement set retarding agents
EP0166797A1 (fr)	1986-01-08	Compositions de ciment qui contiennent des rétardateurs de prise
CA1223280A (fr)	1987-06-23	Agents retardateurs de prise pour ciments hydrauliques
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
US4102701A (en)	1978-07-25	Plaster compositions containing oxo-polycarboxylic acids as a set retarder
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
EP0172282A1 (fr)	1986-02-26	Utilisation des dérivés polymères de pipérazine d'acide phosphorique alkylène comme composés retardateurs de la prise de boues cimenteuses
EP0330413A2 (fr)	1989-08-30	Procédé pour empêcher la formation de dépôts, compositions et procédé de préparation de telles compositions
CA1228080A (fr)	1987-10-13	Additifs a base de derives d'acide aminomethylenephosphonique pour retarder la prise du ciment
CA1234582A (fr)	1988-03-29	Composition de ciment contenant des retardateurs de prise
WO1985001935A1 (fr)	1985-05-09	Composition modifiee de diamine d'alcene ou de polyamine de polyalcene et pate de ciment hydraulique aqueuse utilisant cette composition
NO842458L (no)	1985-12-20	Nye dicyklopentadien-derivater, og fremgangsmaate for aa hemme utfelling av metallioner ved hjelp av disse.
NO842635L (no)	1985-12-30	Fremgangsmaate til aa retardere stivningen av vandige sementvellinger.
NO165672B (no)	1990-12-10	Fremgangsmaate for retardering av stoerkningen av en vandigsementoppslemming ved tilsetning av metylenfosfonsyre-preparater fremstilt ut fra aminohydrokarbyl-piperazin-urinstoffaddukter.
NO842634L (no)	1985-12-30	Fremgangsmaate til aa retardere stivningen av vandige sement-vellinger.
CA1216742A (fr)	1987-01-20	Methode et composition de traitement de forages
EP2125842B1 (fr)	2014-05-21	Procédé de fabrication d'acides alkylamino-alkylènephosphoniques
EP0024880B1 (fr)	1984-02-15	Procédé pour fabriquer un liquide thixotrope