CA1278797C - Concrete admixture compositions - Google Patents
Concrete admixture compositionsInfo
- Publication number
- CA1278797C CA1278797C CA000547111A CA547111A CA1278797C CA 1278797 C CA1278797 C CA 1278797C CA 000547111 A CA000547111 A CA 000547111A CA 547111 A CA547111 A CA 547111A CA 1278797 C CA1278797 C CA 1278797C
- Authority
- CA
- Canada
- Prior art keywords
- weight
- component
- parts
- cement
- concrete
- 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.)
- Expired - Lifetime
Links
- 239000004567 concrete Substances 0.000 title claims abstract description 52
- 239000000203 mixture Substances 0.000 title claims abstract description 33
- 239000011083 cement mortar Substances 0.000 claims abstract description 10
- 230000008014 freezing Effects 0.000 claims abstract description 10
- 238000007710 freezing Methods 0.000 claims abstract description 10
- 229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 4
- 230000000994 depressogenic effect Effects 0.000 claims abstract description 3
- 239000008030 superplasticizer Substances 0.000 claims abstract description 3
- 239000004568 cement Substances 0.000 claims description 26
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 claims description 13
- VPVSTMAPERLKKM-UHFFFAOYSA-N glycoluril Chemical compound N1C(=O)NC2NC(=O)NC21 VPVSTMAPERLKKM-UHFFFAOYSA-N 0.000 claims description 8
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 7
- AIJULSRZWUXGPQ-UHFFFAOYSA-N Methylglyoxal Chemical compound CC(=O)C=O AIJULSRZWUXGPQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 6
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 claims description 4
- 159000000000 sodium salts Chemical group 0.000 claims description 4
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 claims description 3
- KZTWONRVIPPDKH-UHFFFAOYSA-N 2-(piperidin-1-yl)ethanol Chemical compound OCCN1CCCCC1 KZTWONRVIPPDKH-UHFFFAOYSA-N 0.000 claims description 2
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 claims description 2
- YIROYDNZEPTFOL-UHFFFAOYSA-N 5,5-Dimethylhydantoin Chemical compound CC1(C)NC(=O)NC1=O YIROYDNZEPTFOL-UHFFFAOYSA-N 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 2
- 229920006243 acrylic copolymer Polymers 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical class O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims description 2
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 claims description 2
- 229940091173 hydantoin Drugs 0.000 claims description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 2
- 150000002823 nitrates Chemical class 0.000 claims description 2
- 150000002826 nitrites Chemical class 0.000 claims description 2
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 claims description 2
- 229950005308 oxymethurea Drugs 0.000 claims description 2
- 229940120731 pyruvaldehyde Drugs 0.000 claims description 2
- 150000003567 thiocyanates Chemical class 0.000 claims description 2
- 238000009472 formulation Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000011575 calcium Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- VARKIGWTYBUWNT-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanol Chemical compound OCCN1CCN(CCO)CC1 VARKIGWTYBUWNT-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000001465 calcium Nutrition 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 230000009429 distress Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- RAFRTSDUWORDLA-UHFFFAOYSA-N phenyl 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1 RAFRTSDUWORDLA-UHFFFAOYSA-N 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Substances [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010561 standard procedure Methods 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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
-
- 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
-
- 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
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/10—Accelerators; Activators
- C04B2103/12—Set accelerators
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/76—Use at unusual temperatures, e.g. sub-zero
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- On-Site Construction Work That Accompanies The Preparation And Application Of Concrete (AREA)
Abstract
CONCRETE ADMIXTURE COMPOSITIONS
Abstract of the Disclosure A chloride-free cold-weather set accelerator for concrete and cement mortar comprises A) 100 parts by weight of at least one soluble inorganic salt having freezing point depressant properties B) from 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) from 0 to 10 parts by weight of at least one organic set accelerator.
Abstract of the Disclosure A chloride-free cold-weather set accelerator for concrete and cement mortar comprises A) 100 parts by weight of at least one soluble inorganic salt having freezing point depressant properties B) from 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) from 0 to 10 parts by weight of at least one organic set accelerator.
Description
1~78~7~3~7 CONCRElE ADMIXTURE CCMPC6ITIoNS
This invention relates to concrete admixtures for use as cold weather concrete set accelerators.
Low or freezing temperatures (e.g. 5C to -7C) present special problems in the mixing, pouring and curing of concrete. Concrete may freeze while saturated and su~sequently be of low strength, or there may be a slow develcpnent of strength.
m e American Concrete Institute (ACI) Report 306R-78 on Cold Weather concreting, sets forth standard practices to prevent freezing and assure the safe development of concrete strength during curing at ambient freezing conditions. Heating of materials, including mix water and aggregates is mandatory. Protective insulating coverings, heated enclosures and proper curing conditions are described.
An additional factor (not often reported) associated with freezing temperatures, is the distress of the concrete worker operating under adverse conditions. Even if dressed warmly, the conrete worker wishes to finish a pour or complete the finishing as fast as possible, and move indoors out of the wind and cold. Thus, an accelerated set time is an important aspect of cold weather concreting.
While the prior art has addressed the problems of using concrete in cold weather (e.g. the use of calcium chloride as the principle accelerating admixture), it has not successfully developed ~'~7~3~797 admixtures which are, (1) non-corrosive, and (2) meet or exceed at -10C to 5C the rate-of-hardening and compressive strength performance of a plain concrete mix at 10C.
It has now been found that set accelerating admixtures in specific proportions can be obtained which conbine two beneficial effects:
1) They depress the mix water and pore water freezing point, so that a concrete mix will not freeze during the first few critical hours of curing at temperatures below 0C and 2) They reduce the quantity of mix water necessary for curing, which improves early concrete strength development. The reduction in mix water also has an effect on freezing point depression, because it allows for a more concentrated solution of the admixture.
Accordingly, the present invention provides a chloride-free admixture for use as a cold weather concrete set accelerator which comprises A) 100 parts by weight of at least one soluble inorganic salt having freezing point depressant properties B) frcm 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) frcm 0 to 10 parts by weight of at least one organic set accelerator.
Preferably the quantity of component B should be greater than 15 parts by weight.
~78~7~7 Preferably the quantity of camponent C is from 5 to 10 parts by weight.
Preferably ccmponent D i5 present in an amount of fram 1.3 to 6 parts by weight.
The proportions given above are parts by dry weight of the total dry weight of camponents A-D, neglecting any water which may be present. The admixture of the invention may be added as a solid direct to the concrete mix water, or may be used in aqueous solution for addition to the mix water. Preferably the admixture is in the form of an aqueous solution.
Camponent A is preferably selected fram ammonium, alkali and alkaline earth nitrates and nitrites, more preferably fram calcium and sodium nitrate and nitrite. Calcium nitrate is particularly preferred. Up to 50% of the inorganic salt of camponent A may be eeplaced by urea.
Camponent B is preferably an alkali or alkaline earth salt of a naphthalene sulphonate/formaldehyde condensate or a sulphonated melamine/formaldehyde condensate, more preferably a sodium or calcium salt, or an acrylic copolymer for example poly(hydroxyethyl methacrylate/acrylic acid). Particularly preferred is naphthalene sulphonate/formaldehyde condensate in sodium salt form.
Camponent C is preferably selected from ammonium, alkali or alkaline earth thiocyanates and thiosulphates, more preferably from calcium, ammonium and sodium thiocyanates and thiosulphates.
Particularly preferred as camponent C is sodium thiocyanate.
Component D is preferably selected fram methylolglycolurils, dimethylolurea, mono- and di-(N-methylol) hydantoin, mono- and di-(N-methylol) dimethylhydantoin, N-methylolacrylamide, tri-(N-methylol) melamine, N-nydroxyethylpiperidine, N,N-bis(2-hydroxyethyl)piperazine, glutaraldehyde, pyruvaldehyde, furfural and water soluble urea-formaldehyde resins. More preferably, 1~78~9~
This invention relates to concrete admixtures for use as cold weather concrete set accelerators.
Low or freezing temperatures (e.g. 5C to -7C) present special problems in the mixing, pouring and curing of concrete. Concrete may freeze while saturated and su~sequently be of low strength, or there may be a slow develcpnent of strength.
m e American Concrete Institute (ACI) Report 306R-78 on Cold Weather concreting, sets forth standard practices to prevent freezing and assure the safe development of concrete strength during curing at ambient freezing conditions. Heating of materials, including mix water and aggregates is mandatory. Protective insulating coverings, heated enclosures and proper curing conditions are described.
An additional factor (not often reported) associated with freezing temperatures, is the distress of the concrete worker operating under adverse conditions. Even if dressed warmly, the conrete worker wishes to finish a pour or complete the finishing as fast as possible, and move indoors out of the wind and cold. Thus, an accelerated set time is an important aspect of cold weather concreting.
While the prior art has addressed the problems of using concrete in cold weather (e.g. the use of calcium chloride as the principle accelerating admixture), it has not successfully developed ~'~7~3~797 admixtures which are, (1) non-corrosive, and (2) meet or exceed at -10C to 5C the rate-of-hardening and compressive strength performance of a plain concrete mix at 10C.
It has now been found that set accelerating admixtures in specific proportions can be obtained which conbine two beneficial effects:
1) They depress the mix water and pore water freezing point, so that a concrete mix will not freeze during the first few critical hours of curing at temperatures below 0C and 2) They reduce the quantity of mix water necessary for curing, which improves early concrete strength development. The reduction in mix water also has an effect on freezing point depression, because it allows for a more concentrated solution of the admixture.
Accordingly, the present invention provides a chloride-free admixture for use as a cold weather concrete set accelerator which comprises A) 100 parts by weight of at least one soluble inorganic salt having freezing point depressant properties B) frcm 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) frcm 0 to 10 parts by weight of at least one organic set accelerator.
Preferably the quantity of component B should be greater than 15 parts by weight.
~78~7~7 Preferably the quantity of camponent C is from 5 to 10 parts by weight.
Preferably ccmponent D i5 present in an amount of fram 1.3 to 6 parts by weight.
The proportions given above are parts by dry weight of the total dry weight of camponents A-D, neglecting any water which may be present. The admixture of the invention may be added as a solid direct to the concrete mix water, or may be used in aqueous solution for addition to the mix water. Preferably the admixture is in the form of an aqueous solution.
Camponent A is preferably selected fram ammonium, alkali and alkaline earth nitrates and nitrites, more preferably fram calcium and sodium nitrate and nitrite. Calcium nitrate is particularly preferred. Up to 50% of the inorganic salt of camponent A may be eeplaced by urea.
Camponent B is preferably an alkali or alkaline earth salt of a naphthalene sulphonate/formaldehyde condensate or a sulphonated melamine/formaldehyde condensate, more preferably a sodium or calcium salt, or an acrylic copolymer for example poly(hydroxyethyl methacrylate/acrylic acid). Particularly preferred is naphthalene sulphonate/formaldehyde condensate in sodium salt form.
Camponent C is preferably selected from ammonium, alkali or alkaline earth thiocyanates and thiosulphates, more preferably from calcium, ammonium and sodium thiocyanates and thiosulphates.
Particularly preferred as camponent C is sodium thiocyanate.
Component D is preferably selected fram methylolglycolurils, dimethylolurea, mono- and di-(N-methylol) hydantoin, mono- and di-(N-methylol) dimethylhydantoin, N-methylolacrylamide, tri-(N-methylol) melamine, N-nydroxyethylpiperidine, N,N-bis(2-hydroxyethyl)piperazine, glutaraldehyde, pyruvaldehyde, furfural and water soluble urea-formaldehyde resins. More preferably, 1~78~9~
ccmponent D is selected from methylolglycolurils, e.g.
tri-(N-methylol)glycoluril and tetra (N-methylol)glycoluril, particularly tetra (N-methylol)glycoluril.
A preferred admixture accordincl to the invention consists of A) calcium nitrate, B) sodium salt of naphthalene sulphonate/
formaldehyde condensate, C) sodium thiocyanate and D) tetra(N-methylol)glycoluril, in the proportions by weight given above. Particularly preferred is a mixture of the above four ccmponents in the proportions by weight: lO0 parts A), 20 parts B), 6.7 parts C) and 4 parts D). This preferred admixture is preferably used in the form of an aqueous solution containing 40-60~ dry weight of ccmponents A-D, particularly 50% wt.
The admixtures of the invention may be used over a wide range of temperatures from about 20C to about -15C. The amount of admixture which is added to the concrete may be frcm 0.13 to 5.6 parts (dry weight) per 100 parts dry weight of cementitious material in the concrete (e.g. portland cement plus pozzolanic material such as fly ash) preferably 0.65 to 5.6 parts. For the above preferred admixture, the dose range is frcm 1.3 to 4.6 parts / 100 parts cement, and the lower the ambient temperature the higher will be the dosage required. Thus a dosage of 2.6 parts / lO0 parts cement of the preferred admixture will prevent a concrete mix frcm freezing at temperatures down to about -10C, while for lower temperatures a dosage of 3.9 parts / 100 parts cement is preferred.
While the admixture of the invention may be used with any of ASTM type I to V cements, types I and II are preferred. The admixtures may be used in cement mortars as well as in concrete.
The invention also provides a method for accelerating the set of a concrete or cement mortar mix, suitable for use in cold weather conditions, ccmprising adding to the mix frcm 0.65 to 5.6 parts (dry weight) of an admixture according to the invention per 100 parts dry weight of cementitious material in the mix. The concrete or cement 1'~7~3'737 mortar so obtained will contain the following amounts of components A-D, defined above:
CcmPonent ~arts / 100 parts cement A 0.5 - 4.0 B 0.1 - 0.8 C 0.033 - 0.6 D 0.0 - 0.16, preferably 0.02 - 0.16 Preferred amounts are:
Component parts / 100 parts cement A 2.0 - 3.0 B 0.4 - 0.6 C 0.1 - 0.6 D 0.04 - 0.12 Consequently, a similar method which may be substituted for that already described, conprises adding to the concrete or cement mortar 1) 0.5 to 4 % by weight of cement of at least one component A), 20 2) 0.1 to 0.8 % by weight of cement of at least one component ~), 3) 0.033 to 0.6 % by weight of cement of at least one component C) and 4) 0 to 0.16 % of cement of at least one component D.
In the preferred method, at least one ccmponent D is added in the amount of frcm 0.02 to 0.16 % wt. of cement.
The following Examples illustrate the invention. All parts and percentages are by weight unless indicated otherwise.
78'797 Examples Standard procedure A concrete mix without addition of any admixtures of the invention (herein referred to as plain reference) is prepared according to the following formulation:
ccmponent Kg / m_ of concrete Cement of ASTM type I 307 Aggregate 1900 (Sand to stone ratio of 40:60 to 50:50; the stone used is about 2 cm topsided crushed limestone) W~ter as indicated in Tables III to VII.
An air-entraining admixture may also be added. Those used are sold by Master Builders Inc. (Cleveland, Ohio) under the trade marks Micro-Air, and Master ~uilders Neutralised Vinsol, respectively. Both meet the requirements of ASTM C-260, AASHTO M-154 and CRD-C13.
Concrete mixes with addition of admixtures of the invention are prepared according to the concrete formulation of the plain reference. Mixing together the concrete component and the admixtures is carried out as follows:
Mix water in the amount of about 80 % of that of the plain reference is added to a conventional cement mixer and the admixture then added to the water. The cement, sand and stone are further added.
Then the remaining 20 % of water is used in part to adjust the slump to the slump of the plain reference.
l~7a~7~7 The concrete is then poured into 10 cm cubes which are covered to prevent moisture loss. The concrete cubes are stored for the time and at the temperature indicated in Examples I to VI.
Properties The following properties are routinely measured:
Slump, i.e. the drop in cm of a 12 inch (30.5 cm) high cone of the fresh mix. (ASTM C 143) Percent~ge of entrained air ~ater Reduction i.e. the difference between the amount of water used in the plain reference and the (smaller) amount of water used in the test sample in order to obtain the same slump, expressed as a percentage of the amount of water used in the plain reference.
Cqqpressive Strength, expressed in Kg/cm2 and as a percentage of the campressive strength of the plain reference measured under the same conditions.
Rate of ~ardening (~CH), i.e. the time in hours to reach the initial set.
(ASTM C 403) 1'~78'7'~37 Examples 1-26 Tables I and II list admixture formulations according to the invention, given as parts by weight of components B), C) and D per 100 parts by weight of component A). These formulations are each dissolved in water such that the aqueous solution contains 3 lb (1 36 kg) of component A) in 90 flui~ ounces (2.56 litres) of solution. AS the specific gravity of these solutions is approx. 1.39, the solutions of the admixture formulations all contain 1.36 kg component A) in 3.56 kg solution, or 38% by wt. component A). With the other components, the solutions contain a total of approx.
50% wt. active material.
1~78~ 37 Table I
Admixtures 1-18, each containing 100 parts by weight of calcium nitrate A), and in addition:
parts by weight B) Na salt of naphthalene C) sodium D) tetra(N-Example No. sulphonate/formaldehyde thiocya- methylol) nate glycoluril 1 20 6.7 3.3 3 20 20 1.6 4 20 6.7 4 6.7 1.3 6 13.3 20 4 7 13.3 20 1.3 8 13.3 6.7 4 9 13.3 6.7 1.3 16 3.2 1'~78~97 Table II
Admixtures 19-26 Formulation tparts by weight) Example No. 19 20 21 22 23 24 25 26 Camponent A) Calcium nitrate 100 100 - 66.7 100 100 100 100 calcium nitrite -- 100 33.3 - - - -B) naphthalene sulphonate/
formaldehyde Ca salt 20 20 Na salt - - 20 20 20 20 20 20 C) Sodium thiocyanate 6.7 - - 6.7 6.7 6.7 6.7 6.7 Ammonium thiocyanate - 6.7 6.7 D) tetra(N-methylol) glycoluril 4 4 4 4 pyruvic aldehyde - - - - 4 glutaraldehyde - - - - - - 4 N-hydroxyethyl piperidine - - - - - 4 N,N'-bis-(2-hydroxy-ethyl)piperazine - - - - - - - 4 Sodium acetate 1.4 1.4 1.4 1.4 1.4 1.4 1.4 1.4 (buffer) 1'c:7~7~37 In the following Examples, the admixture solutions are added to the test concrete in quantities sufficient to give the indicated dose, given as parts by weight of total admixture (excluding water~
per 100 lb of cement.
Example 27 An outdoor experiment was carried out in which all the concrete samples, including the plain concrete reference, were mixed at 5C
and poured at -7 to -8C. During the curing time, the outdoor temperature varied from -15C to +18C.
The results are indicated in Table III. Trial 1 shows the optimum results which are obtained with the already known corrosive CaC12 admixture while trials 2 and 3 demonstrate that similar results can be obtained when using a non-corrosive admixture of the invention.
Example 28 Plain concrete is made, poured and cured at 10C while concrete samples of trials 1 to 5 are made at 10C, cured at -8 to -6C for 3 days and then cured at 10C.
In the trials, the admixtures of examples 1 and 4 (of very similar composition) are added in dosages of from approx. 2 to 4.5 parts/100 parts cement. In all cases the rate of hardening is more rapid than that of the plain concrete at 10C, and the 2B day compressive strength is as good as that of the plain concrete.
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~7B797 - 14 - l54-oog2 Example 2g Two plain concrete samples are prepared, one of which (trial 0) is made, poured and cured at 10C, while the other (trial 1) is made at 10C, then poured and cured for 3 days at -3C, then further cured at 10C. Trial 2 is as trial 1, but contains 3.48 parts / 100 parts cement of the admixture formulation of Example 10. The results are shcwn in Table V.
Example 30 A plain concrete sample is made, poured and cured at 10C while concrete samples of trials 1 to 17 are made at 10C, poured and cured for 1 day at -5C; then the 28 day samples are cured at 10C.
Results shown in Table VI demonstrate that, compared to the plain concrete reference, the time to reach the initial setting (rate of hardening) of trials 1 to 17 is largely reduced, and that the campressive strength performances after 28 days are superior. The trial samples did not freeze at the -5C temperature.
Example 31 The plain concrete and concrete of trials 1 to 3 ~containing the admixture of Example 4) are all made, poured and cured at 21C.
Results are shown in Table VII. The admixtures of the invention are shown to be effective at this higher temperature.
Example 32 Two plain concretes are prepared. One (trial 0) is made and cured at 10C. The other one (trial 1), like the concrete samples of trials 2 to 9, is made at 3-5C, cured for 3 days at a temperature which varies from -15 to 0C, and then cured at a temperature which varies fram -15 to 5C.
Results are shown in Table VIII.
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tri-(N-methylol)glycoluril and tetra (N-methylol)glycoluril, particularly tetra (N-methylol)glycoluril.
A preferred admixture accordincl to the invention consists of A) calcium nitrate, B) sodium salt of naphthalene sulphonate/
formaldehyde condensate, C) sodium thiocyanate and D) tetra(N-methylol)glycoluril, in the proportions by weight given above. Particularly preferred is a mixture of the above four ccmponents in the proportions by weight: lO0 parts A), 20 parts B), 6.7 parts C) and 4 parts D). This preferred admixture is preferably used in the form of an aqueous solution containing 40-60~ dry weight of ccmponents A-D, particularly 50% wt.
The admixtures of the invention may be used over a wide range of temperatures from about 20C to about -15C. The amount of admixture which is added to the concrete may be frcm 0.13 to 5.6 parts (dry weight) per 100 parts dry weight of cementitious material in the concrete (e.g. portland cement plus pozzolanic material such as fly ash) preferably 0.65 to 5.6 parts. For the above preferred admixture, the dose range is frcm 1.3 to 4.6 parts / 100 parts cement, and the lower the ambient temperature the higher will be the dosage required. Thus a dosage of 2.6 parts / lO0 parts cement of the preferred admixture will prevent a concrete mix frcm freezing at temperatures down to about -10C, while for lower temperatures a dosage of 3.9 parts / 100 parts cement is preferred.
While the admixture of the invention may be used with any of ASTM type I to V cements, types I and II are preferred. The admixtures may be used in cement mortars as well as in concrete.
The invention also provides a method for accelerating the set of a concrete or cement mortar mix, suitable for use in cold weather conditions, ccmprising adding to the mix frcm 0.65 to 5.6 parts (dry weight) of an admixture according to the invention per 100 parts dry weight of cementitious material in the mix. The concrete or cement 1'~7~3'737 mortar so obtained will contain the following amounts of components A-D, defined above:
CcmPonent ~arts / 100 parts cement A 0.5 - 4.0 B 0.1 - 0.8 C 0.033 - 0.6 D 0.0 - 0.16, preferably 0.02 - 0.16 Preferred amounts are:
Component parts / 100 parts cement A 2.0 - 3.0 B 0.4 - 0.6 C 0.1 - 0.6 D 0.04 - 0.12 Consequently, a similar method which may be substituted for that already described, conprises adding to the concrete or cement mortar 1) 0.5 to 4 % by weight of cement of at least one component A), 20 2) 0.1 to 0.8 % by weight of cement of at least one component ~), 3) 0.033 to 0.6 % by weight of cement of at least one component C) and 4) 0 to 0.16 % of cement of at least one component D.
In the preferred method, at least one ccmponent D is added in the amount of frcm 0.02 to 0.16 % wt. of cement.
The following Examples illustrate the invention. All parts and percentages are by weight unless indicated otherwise.
78'797 Examples Standard procedure A concrete mix without addition of any admixtures of the invention (herein referred to as plain reference) is prepared according to the following formulation:
ccmponent Kg / m_ of concrete Cement of ASTM type I 307 Aggregate 1900 (Sand to stone ratio of 40:60 to 50:50; the stone used is about 2 cm topsided crushed limestone) W~ter as indicated in Tables III to VII.
An air-entraining admixture may also be added. Those used are sold by Master Builders Inc. (Cleveland, Ohio) under the trade marks Micro-Air, and Master ~uilders Neutralised Vinsol, respectively. Both meet the requirements of ASTM C-260, AASHTO M-154 and CRD-C13.
Concrete mixes with addition of admixtures of the invention are prepared according to the concrete formulation of the plain reference. Mixing together the concrete component and the admixtures is carried out as follows:
Mix water in the amount of about 80 % of that of the plain reference is added to a conventional cement mixer and the admixture then added to the water. The cement, sand and stone are further added.
Then the remaining 20 % of water is used in part to adjust the slump to the slump of the plain reference.
l~7a~7~7 The concrete is then poured into 10 cm cubes which are covered to prevent moisture loss. The concrete cubes are stored for the time and at the temperature indicated in Examples I to VI.
Properties The following properties are routinely measured:
Slump, i.e. the drop in cm of a 12 inch (30.5 cm) high cone of the fresh mix. (ASTM C 143) Percent~ge of entrained air ~ater Reduction i.e. the difference between the amount of water used in the plain reference and the (smaller) amount of water used in the test sample in order to obtain the same slump, expressed as a percentage of the amount of water used in the plain reference.
Cqqpressive Strength, expressed in Kg/cm2 and as a percentage of the campressive strength of the plain reference measured under the same conditions.
Rate of ~ardening (~CH), i.e. the time in hours to reach the initial set.
(ASTM C 403) 1'~78'7'~37 Examples 1-26 Tables I and II list admixture formulations according to the invention, given as parts by weight of components B), C) and D per 100 parts by weight of component A). These formulations are each dissolved in water such that the aqueous solution contains 3 lb (1 36 kg) of component A) in 90 flui~ ounces (2.56 litres) of solution. AS the specific gravity of these solutions is approx. 1.39, the solutions of the admixture formulations all contain 1.36 kg component A) in 3.56 kg solution, or 38% by wt. component A). With the other components, the solutions contain a total of approx.
50% wt. active material.
1~78~ 37 Table I
Admixtures 1-18, each containing 100 parts by weight of calcium nitrate A), and in addition:
parts by weight B) Na salt of naphthalene C) sodium D) tetra(N-Example No. sulphonate/formaldehyde thiocya- methylol) nate glycoluril 1 20 6.7 3.3 3 20 20 1.6 4 20 6.7 4 6.7 1.3 6 13.3 20 4 7 13.3 20 1.3 8 13.3 6.7 4 9 13.3 6.7 1.3 16 3.2 1'~78~97 Table II
Admixtures 19-26 Formulation tparts by weight) Example No. 19 20 21 22 23 24 25 26 Camponent A) Calcium nitrate 100 100 - 66.7 100 100 100 100 calcium nitrite -- 100 33.3 - - - -B) naphthalene sulphonate/
formaldehyde Ca salt 20 20 Na salt - - 20 20 20 20 20 20 C) Sodium thiocyanate 6.7 - - 6.7 6.7 6.7 6.7 6.7 Ammonium thiocyanate - 6.7 6.7 D) tetra(N-methylol) glycoluril 4 4 4 4 pyruvic aldehyde - - - - 4 glutaraldehyde - - - - - - 4 N-hydroxyethyl piperidine - - - - - 4 N,N'-bis-(2-hydroxy-ethyl)piperazine - - - - - - - 4 Sodium acetate 1.4 1.4 1.4 1.4 1.4 1.4 1.4 1.4 (buffer) 1'c:7~7~37 In the following Examples, the admixture solutions are added to the test concrete in quantities sufficient to give the indicated dose, given as parts by weight of total admixture (excluding water~
per 100 lb of cement.
Example 27 An outdoor experiment was carried out in which all the concrete samples, including the plain concrete reference, were mixed at 5C
and poured at -7 to -8C. During the curing time, the outdoor temperature varied from -15C to +18C.
The results are indicated in Table III. Trial 1 shows the optimum results which are obtained with the already known corrosive CaC12 admixture while trials 2 and 3 demonstrate that similar results can be obtained when using a non-corrosive admixture of the invention.
Example 28 Plain concrete is made, poured and cured at 10C while concrete samples of trials 1 to 5 are made at 10C, cured at -8 to -6C for 3 days and then cured at 10C.
In the trials, the admixtures of examples 1 and 4 (of very similar composition) are added in dosages of from approx. 2 to 4.5 parts/100 parts cement. In all cases the rate of hardening is more rapid than that of the plain concrete at 10C, and the 2B day compressive strength is as good as that of the plain concrete.
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~7B797 - 14 - l54-oog2 Example 2g Two plain concrete samples are prepared, one of which (trial 0) is made, poured and cured at 10C, while the other (trial 1) is made at 10C, then poured and cured for 3 days at -3C, then further cured at 10C. Trial 2 is as trial 1, but contains 3.48 parts / 100 parts cement of the admixture formulation of Example 10. The results are shcwn in Table V.
Example 30 A plain concrete sample is made, poured and cured at 10C while concrete samples of trials 1 to 17 are made at 10C, poured and cured for 1 day at -5C; then the 28 day samples are cured at 10C.
Results shown in Table VI demonstrate that, compared to the plain concrete reference, the time to reach the initial setting (rate of hardening) of trials 1 to 17 is largely reduced, and that the campressive strength performances after 28 days are superior. The trial samples did not freeze at the -5C temperature.
Example 31 The plain concrete and concrete of trials 1 to 3 ~containing the admixture of Example 4) are all made, poured and cured at 21C.
Results are shown in Table VII. The admixtures of the invention are shown to be effective at this higher temperature.
Example 32 Two plain concretes are prepared. One (trial 0) is made and cured at 10C. The other one (trial 1), like the concrete samples of trials 2 to 9, is made at 3-5C, cured for 3 days at a temperature which varies from -15 to 0C, and then cured at a temperature which varies fram -15 to 5C.
Results are shown in Table VIII.
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Claims (17)
1. A chloride-free admixture for use as a cold weather concrete set accelerator which ccmprises A) 100 parts by weight of at least one soluble inorganic salt having freezing point depressant properties, up to 50% wt.
of which may be replaced by urea B) from 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) from 0 to 10 parts by weight of at least one organic set accelerator.
of which may be replaced by urea B) from 13.3 to 30 parts by weight of at least one superplasticizer C) from 3 to 30 parts by weight of at least one inorganic early set and strength accelerator, and D) from 0 to 10 parts by weight of at least one organic set accelerator.
2. An admixture according to Claim 1 comprising 100 parts by weight A), from above 15 to 30 parts by weight B), 5 to 10 parts by weight C) and 1.3 to 6 parts by weight D).
3. An admixture according to Claim 1 in which component A is selected from ammonium, alkali and alkaline earth nitrates and nitrites.
4. An admixture according to Claim 3 in which component A is calcium nitrate,
5. An admixture according to Claim 1 in which component B is an alkali or alkaline earth salt of a naphthalene sulphonate/formaldehyde condensate or a sulphonated melamine/formaldehyde condensate, or an acrylic copolymer.
6. An admixture according to Claim 5 in which component B is naphthalene sulphonate/formaldehyde condensate in sodium salt form.
7. An admixture according to CLaim 1 in which ccmponent C is selected from ammonium, alkali or alkaline earth thiocyanates and thiosulphates.
8. An admixture according to Claim 7 in which component C is sodium thiocyanate.
9. An admixture according to Claim 1 in which component D is selected from methylolglycolurils, dimethylolurea, mono- and di-(N-methylol) hydantoin, mono- and di-(N-methylol) dimethylhydantoin, N-methylolacrylamide, tri-(N-methylol) melamine, N-hydroxyethylpiperidine, N,N-bis(2-hydroxyethyl)piperazine, glutaraldehyde, pyruvaldehyde, furfural and water soluble urea-formaldehyde resins.
10. An admixture according to Claim 9 in which component D is tetra(N-methylol)glycoluril.
11. An admixture according to Claim 2 ccmprising A) 100 parts by weight calcium nitrate B) 20 parts by weight naphthalene sulphonate/formaldehyde condensate sodium salt C) 6.7 parts by weight sodium thiocyanate and D) 4 parts by weight tetra(N-methylol)glycoluril.
12. An admixture according to Claim 1 in the form of an aqueous solution.
13. A method for accelerating the set of a concrete or cement mortar mix, suitable for use in cold weather conditions, comprising adding to the mix from 0.13 to 5.6 parts (dry weight) of an admixture according to Claim 1 per 100 parts dry weight of cementitious material in the mix.
14. A method for accelerating the set of a concrete or cement mortar mix, suitable for use in cold weather conditions, comprising adding to the concrete or cement mortar 1) 0.5 to 4 % by weight of cement of at least one component A), 2) 0.1 to 0.8 % by weight of cement of at least one component B), 3) 0.033 to 0.6 % by weight of cement of at least one component C) and 4) 0 to 0.16 % of cement of at least one component D, in which components A, B, C and D are as defined in Claim 1.
15. A concrete or cement mortar mix containing 1) 0.5 to 4 % by weight of cement of at least one component A), 2) 0.1 to 0.8 % by weight of cement of at least one component B), 3) 0.033 to 0.6 % by weight of cement of at least one component C) and 4) 0 to 0.16 % of cement of at least one component D, in which components A, B, C and D are as defined in Claim 1.
16. A concrete or cement mortar mix according to Claim 15 containing 0.02 to 0.16 % wt. of component D.
17. A concrete or cement mortar mix according to Claim 16 containing 2.0-3.0 % wt. of component A, 0.4-0.6 % wt. of component B, 0.1-0.6 % wt. of component C and 0.04-0.12 % wt. of component D.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90952486A | 1986-09-19 | 1986-09-19 | |
US909,524 | 1986-09-19 |
Publications (1)
Publication Number | Publication Date |
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CA1278797C true CA1278797C (en) | 1991-01-08 |
Family
ID=25427379
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000547111A Expired - Lifetime CA1278797C (en) | 1986-09-19 | 1987-09-17 | Concrete admixture compositions |
Country Status (11)
Country | Link |
---|---|
JP (1) | JPS6389445A (en) |
AT (1) | AT393498B (en) |
AU (1) | AU592013B2 (en) |
BE (1) | BE1002419A4 (en) |
CA (1) | CA1278797C (en) |
CH (1) | CH675716A5 (en) |
DE (1) | DE3730527A1 (en) |
ES (1) | ES2005013A6 (en) |
FR (1) | FR2604170B1 (en) |
GB (1) | GB2195328B (en) |
IT (1) | IT1211786B (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2142357A1 (en) * | 1992-09-01 | 1994-03-17 | Paul Scheiner | Hydraulic cement bughole-reducing admixtures and method for using same |
GB9505259D0 (en) * | 1995-03-16 | 1995-05-03 | Sandoz Ltd | Improvements in or relating to organic compounds |
CA2262855C (en) * | 1997-05-15 | 2007-11-20 | Mbt Holding Ag | A cementitious mixture containing high pozzolan cement replacement and compatibilizing admixtures therefor |
JP4656471B2 (en) * | 2000-12-18 | 2011-03-23 | 建設省近畿地方建設局長 | Rear impact impact mitigation device |
US7247201B2 (en) * | 2004-10-07 | 2007-07-24 | Ronald Barbour | Pre-blend cement compositions containing non-chloride accelerators |
NO20121086A1 (en) | 2012-09-25 | 2014-03-26 | Yara Int Asa | Antifreeze composition for production of resistant concrete under cold temperature conditions |
NO20131392A1 (en) | 2013-10-21 | 2015-04-22 | Yara Int Asa | |
CN113039169A (en) * | 2019-01-08 | 2021-06-25 | Sika技术股份公司 | Cement-based compositions with accelerated curing at low temperatures |
CN110615638A (en) * | 2019-10-15 | 2019-12-27 | 天津冶建特种材料有限公司 | Low-temperature-resistant liquid alkali-free setting accelerator and preparation method thereof |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU417388A1 (en) * | 1972-02-04 | 1974-02-28 | ||
SU814930A1 (en) * | 1978-06-13 | 1981-03-23 | Bychvarov Nikola Khristov | Complex additive to cement-concrete mix |
JPS5820896A (en) * | 1981-07-28 | 1983-02-07 | 植村 厚一 | Blade port |
DE3276699D1 (en) * | 1982-05-10 | 1987-08-13 | Sandoz Ag | Admixture for cold-weather concrete |
JPS58199760A (en) * | 1982-05-12 | 1983-11-21 | 日曹マスタ−ビルダ−ズ株式会社 | Admixing agent for concrete in cold circumstances |
FI66414C (en) * | 1982-10-08 | 1984-10-10 | Veli Sarkkinen | FOERFARANDE FOER FRAMSTAELLNING AV LIGNOSULFONATBASERADE BLANDNINGAR FOER ANVAENDNING I SYNNERHET SAOSOM TILLSATSAEMNEN FOR BETONG |
US4473405A (en) * | 1983-04-11 | 1984-09-25 | Martin Marietta Corporation | Admixture for hydraulic cement |
JPS6021840A (en) * | 1983-07-12 | 1985-02-04 | 日曹マスタ−ビルダ−ズ株式会社 | Cement composition |
US4606770A (en) * | 1984-11-13 | 1986-08-19 | Sandoz Ltd. | Additive for hydraulic cement mixes |
JPS61141649A (en) * | 1984-12-14 | 1986-06-28 | 日産化学工業株式会社 | Cement composition |
-
1987
- 1987-09-11 DE DE3730527A patent/DE3730527A1/en not_active Withdrawn
- 1987-09-14 BE BE8701031A patent/BE1002419A4/en not_active IP Right Cessation
- 1987-09-14 CH CH3537/87A patent/CH675716A5/de not_active IP Right Cessation
- 1987-09-14 FR FR8712734A patent/FR2604170B1/en not_active Expired - Lifetime
- 1987-09-15 GB GB8721701A patent/GB2195328B/en not_active Expired - Lifetime
- 1987-09-17 CA CA000547111A patent/CA1278797C/en not_active Expired - Lifetime
- 1987-09-17 ES ES8702679A patent/ES2005013A6/en not_active Expired
- 1987-09-17 AU AU78480/87A patent/AU592013B2/en not_active Expired
- 1987-09-17 IT IT8748397A patent/IT1211786B/en active
- 1987-09-18 AT AT2359/87A patent/AT393498B/en not_active IP Right Cessation
- 1987-09-18 JP JP62232693A patent/JPS6389445A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
ATA235987A (en) | 1991-04-15 |
AU7848087A (en) | 1988-03-24 |
AU592013B2 (en) | 1989-12-21 |
GB2195328B (en) | 1990-04-18 |
BE1002419A4 (en) | 1991-02-05 |
JPS6389445A (en) | 1988-04-20 |
FR2604170B1 (en) | 1992-11-06 |
CH675716A5 (en) | 1990-10-31 |
GB2195328A (en) | 1988-04-07 |
IT8748397A0 (en) | 1987-09-17 |
FR2604170A1 (en) | 1988-03-25 |
AT393498B (en) | 1991-10-25 |
IT1211786B (en) | 1989-11-03 |
GB8721701D0 (en) | 1987-10-21 |
ES2005013A6 (en) | 1989-02-16 |
DE3730527A1 (en) | 1988-03-24 |
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