MXPA99001679A - Fibers having enhanced concrete bonding strength - Google Patents
Fibers having enhanced concrete bonding strengthInfo
- Publication number
- MXPA99001679A MXPA99001679A MXPA/A/1999/001679A MX9901679A MXPA99001679A MX PA99001679 A MXPA99001679 A MX PA99001679A MX 9901679 A MX9901679 A MX 9901679A MX PA99001679 A MXPA99001679 A MX PA99001679A
- Authority
- MX
- Mexico
- Prior art keywords
- carbon atoms
- ether
- group
- fibers
- glycol
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 63
- 239000004567 concrete Substances 0.000 title claims abstract description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 42
- 125000004432 carbon atoms Chemical group C* 0.000 claims abstract description 30
- 239000000463 material Substances 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 21
- -1 glycol ethers Chemical class 0.000 claims abstract description 18
- 239000011248 coating agent Substances 0.000 claims abstract description 17
- 238000000576 coating method Methods 0.000 claims abstract description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 52
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 239000004568 cement Substances 0.000 claims description 14
- 239000004570 mortar (masonry) Substances 0.000 claims description 13
- 239000004743 Polypropylene Substances 0.000 claims description 10
- 229920001155 polypropylene Polymers 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- GYIXQTJAIAZSHP-UHFFFAOYSA-N 2-[2-[(2-methylpropan-2-yl)oxy]propoxy]propan-1-ol Chemical compound OCC(C)OCC(C)OC(C)(C)C GYIXQTJAIAZSHP-UHFFFAOYSA-N 0.000 claims description 7
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 239000006072 paste Substances 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- HDXAQJALAKVYTG-UHFFFAOYSA-N 2,2,6,6-tetramethylheptane-3,4,5-triol Chemical group CC(C)(C)C(O)C(O)C(O)C(C)(C)C HDXAQJALAKVYTG-UHFFFAOYSA-N 0.000 claims description 3
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- XYVAYAJYLWYJJN-UHFFFAOYSA-N 2-(2-propoxypropoxy)propan-1-ol Chemical compound CCCOC(C)COC(C)CO XYVAYAJYLWYJJN-UHFFFAOYSA-N 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 125000005702 oxyalkylene group Chemical group 0.000 abstract description 4
- 210000003666 Nerve Fibers, Myelinated Anatomy 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 239000000080 wetting agent Substances 0.000 description 5
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 4
- 238000011068 load Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 229910014033 C-OH Inorganic materials 0.000 description 3
- 229910014570 C—OH Inorganic materials 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 230000000717 retained Effects 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- DUFKCOQISQKSAV-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol Chemical compound CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000011396 hydraulic cement Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000004154 testing of material Methods 0.000 description 2
- 210000003165 Abomasum Anatomy 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L Calcium hydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 206010061592 Cardiac fibrillation Diseases 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002600 fibrillogenic Effects 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000002209 hydrophobic Effects 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 230000001050 lubricating Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011404 masonry cement Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000003014 reinforcing Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
Abstract
The bonding between concrete and fibers is enhanced by using a fiber coating material selected from certain glycol ethers, having at least three carbon atoms in an oxyalkylene group, and glycerol ethers. The present invention pertains to such coated fibers, a method for modifying a concrete using the coated fibers, and a cementitious composition containing the coated fibers.
Description
"FIBERS THAT HAVE IMPROVED RESISTANCE TO THE ACCESSION TO THE CONCRETE"
FIELD OF THE INVENTION
The present invention relates to fibers for reinforcing concrete and, more particularly, to the use of fibers coated with a material for improving resistance to adhesion to concrete such as glycol ethers and specific glycerol ethers.
BACKGROUND OF THE INVENTION
Fibers made of metal, glass and synthetic materials, such as polyolefins, have been used in concrete, to provide additional tensile strength and to reinforce against impact damage and crack propagation, including self-induced cracks. Polyolefin fibers, such as polypropylene tend to be hydrophobic due to the nature of the material, and require a wetting agent to provide a surface tension characteristic that allows them to be more easily dispersed within an aqueous concrete mixture. U.S. Patent No. 5,399,195 (assigned to Danaklon A / S) described polyolefin fibers which were treated with a wetting agent by passing filament bundles through lubricating application rolls. The wetting agent can be selected from wetting agents normally applied to synthetic fibers to make them hydrophilic such as emulsifiers, surfactants, detergents and mixtures thereof. The examples in the '195 patent included fatty acid esters of glycerides, fatty acid amides, polyglycol esters, polyethoxylated amides, nonionic surfactants and cationic surfactants. Fiber coatings of the prior art, however, are believed by the present inventors, which presents some problems in concrete applications. Some coating formulations that are derived from ethylene oxide or that contain fatty residues can generate air or cause foaming which, adjacent to the surface of the fiber, can increase the tendency of the fiber to be extracted during the formation of cracks. Accordingly, a novel coated fiber, a fiber coating material and a method for modifying concrete properties using a novel coated fiber are necessary.
SUMMARY OF THE INVENTION Overcoming the disadvantages of the prior art, the present invention provides coated fibers having improved resistance to concrete adhesion and improved extraction resistance, and it is believed that they help to suppress the air retention capabilities of the Cement mixture, in which the coated fibers are mixed. The fibers, preferably made of polypropylene, are coated with a material that is selected from specific glycol ethers, having at least three carbon atoms in an oxyalkylene group, and glycerol ethers. A preferred glycol ether fiber coating material is dipropylene glycol-t-butyl ether; while a preferred glycerol ether fiber coating is di-t-butyl glycerol. An exemplary method of the invention for modifying the properties of a concrete comprises adding to the concrete, mortar or cement mixture, an amount of 0.05 percent to 10 percent by weight, and more preferably an amount of 0.1 percent to 5 percent by weight. percent based on the total dry weight of the cement, the fibers having a coating material that is mentioned above; and mixing the resulting mixture. The present invention also relates to cementitious compositions comprising the coated fibers described above.
DETAILED DESCRIPTION OF THE EXEMPLARY MODALITIES
The terms "paste", "mortar" and "concrete" are technical terms: pastes are mixtures composed of a hydraulic cement binder (usually, but not exclusively, Portland cement, Masonry cement or Mortar cement, and also include limestone, hydrated lime, fly ash, blast furnace concrete and silica vapors or other materials commonly included in these cements) and water; mortars are pastes that also include a fine aggregate; and concretes are mortars that also include coarse aggregate. The "cementitious" compositions of the invention can be formed by mixing the required amounts of certain materials, e.g. a hydraulic cement, water and fine or coarse aggregate, as desired, with the coated fibers as will be described below. A method of the present invention for modifying the properties of a concrete comprises: adding to a concrete, mortar or cement mixture, in an amount of 0.05 percent to 10 percent by weight based on the total dry weight of the cement, fibers having a coating material that is selected from the group consisting of glycol ether and glycerol ether; mix the resulting mixture to obtain a concrete, mortar or paste mixture in which the individual fibers are distributed homogeneously; and molding the mixture in one configuration. Most preferably, the amount of addition of the coated fiber is from 0.1 percent to 5 percent, and most preferably, from 0.5 percent to 2 percent, based on the total dry weight of the cement. The term "configuration" means and refers to a wall, floor, panel, block, paver or other component of a building or civil engineering structure, such as a building, parking garage, bridge deck, tunnel and the like, which It is formed by molded concrete. The coated fibers of the invention can also be used in mortars. Exemplary fibers of the invention comprise steel, glass, carbon fiber, cellulose, rayon or synthetic materials such as polyolefins, nylon, polyester, and acrylics. Polyolefins such as polypropylene are preferred. The polypropylene fibers may be in the form of monofilament, confronted fibrillation, tape or other configurations and adhere in a formation of various sizes and dimensions. The fibers can also be packaged using mechanical or chemical means or can still be introduced into cementitious compositions using special packaging technology (See, e.g., North American Patent Number 5,224,774 to W. R. Grace). The fibers of the invention can be coated during or after the fiber manufacturing process, using known methods. Exemplary coated fibers of the present invention are coated with a glycol ether having the formula:
RO (AO) n-H wherein R comprises an alkyl group of 1 to 7 carbon atoms or a cycloalkyl group of 5 to 7 carbon atoms; A comprises an alkylene group of 3 to 4 carbon atoms; Or is oxygen; n represents an integer from 1 to 10, and H is hydrogen. The AO groups (e.g., "oxyalkylene") which form the chain of these glycols may contain a single type of the alkylene ether group or a mixture of alkylene ether groups which may be in a block or random arrangement. The present invention proposes that an oxyalkylene group has at least three carbon atoms. Preferred glycol ethers are: di-propylene glycol t-butyl ether, having the formula CH3 H H H I I I I CH3-C-O-C-C-O-C-C-OH I I I I CH3 H CH3 H CH3 di-propylene glycol-n-butyl ether, having the formula
H H H H l i l i CH3-CH2-CH2-CH2 -O-C-C-O-C-C-OH I I I H CH3 H CH3; Y
di-propylene glycol-n-propyl ether having the formula H H H I I I I CH 3 -CH 2 -CH 2 -O-C-C-O-C-C-OH I I I I H CH 3 H CH 3
Other exemplary coated fibers of the present invention are coated with a glycerol ether having the formula: CH ~ (AO) and-OR2 CH2- (AO) z-OR3
wherein R] _, R2 and R3 are hydrogen or an alkyl group of 1 to 14 carbon atoms, at least one of R] _, R2 and R3 comprises an alkyl group of 1 to 14 carbon atoms; A is a group of 2 to 4 carbon atoms; and x, y and z are integers from 0 to 10.
A preferred glycerol ether is di-t-butylglycerol, which has the formula
CH2 - 0 - C (CH3) 3 I
CH2 - OH I
CH2 - 0 - C (CH3) 3
The invention is further illustrated by the following non-limiting examples.
Example 1
This example illustrates the operation of relative air retention of an ethylene glycol, namely, triethylene glycol monobutyl ether (which can be obtained from Union Carbide under the name "butoxytriglycol"), which is chemically similar to a known wetting agent, the ether of polyethylene glycol lauryl (See, eg column 8, II.10-12, US Patent Number 5,399,195) as compared to the di-propylene glycol-t-butyl ether as proposed in the present invention. A control sample mortar was made using 2 weight percent of an air retention agent (based on the dry weight of the cement). The air retention agent can be obtained from W. R. Grace & Co.-Conn., Of Cambridge, Massachusetts, under the name of DARAVAIR® 1000. A second sample of triethylene glycol monobutyl ether mortar ("butoxytriglyc") was prepared in an amount of 2 percent (by weight). A third sample of mortar containing di-propylene glycol-t-butyl ether ("DPTB") was also prepared in an amount of 2 percent (by weight). The samples were mixed for nine minutes, and the air content was determined in accordance with Method C185 of the American Society for the Testing of Materials (1994). The results are summarized in the following table and show that ethylene glycol ("butoxitriglicol") retained the air in an amount similar to the control sample. However, sample 3 containing DPTB surprisingly showed almost two thirds less of retained air. Table 1
Sample Retained Air (Method C185-1994 of the American Society for the Testing of Materials)
1 Control 24%
2 Butoxytriglycol 20%
3 DPTB 7% Example 2
This test measured the resistance to the extraction of several coated fibers. Polypropylene fibers with a length of 5.08 centimeters and a diameter of .648 x 1.00 millimeters were used to elaborate the three samples. Sample 1 comprised polypropylene fibers having a coating comprising polyethylene glycol monolaurate ("PEG monolaurate"), an ester having a molecular weight of about 400 to 500. Sample 2 was prepared by coating another identical number of polypropylene fibers with butoxitriglicol. Sample 3 was prepared by coating another set of identical fibers with di-propylene glycol t-butyl ether ("DPTB"). The 5.08 centimeter fibers were coated by immersing in coating materials, allowing it to air dry, and then the coated portion was immersed in identical cement pastes (slurry) in such a way that the embedded length of the fibers was 2.54 centimeters. The cement was allowed to cure for 24 hours at 100 percent relative humidity. All three samples were tested on an Instron 1011 tester that measured the load (in kilograms) needed to displace the cement fibers. The resistance to extraction, or the resistance to adhesion (kilograms per square centimeter), was calculated by determining the average maximum load reed to displace the fibers, and dividing it by the average surface area of the fiber that comes into contact with the fiber. Cementitious matrix. The following table summarizes the relative adhesion strengths calculated for each of the three fiber samples. Table 2
Mués - Coating Material - Load Load Resistance Maximum Fiber Traction Average Adhesion (kgs) (kgs) (kgs per cm ^)
PEG monolaurate 1.32 PEG monolaurate 0.91 PEG monolaurate 1.33 l.lí 877
Butoxitriglicol 1.09 Butoxitriglicol 1.18 Butoxitriglicol 1.27 Butoxitriglicol 1.00 Butoxitriglicol 1.77 1.23 915
DPTB 1.27 DPTB 1.63 DPTB 1.36 DPTB 1.54 1.45 1.077 Sample 1 demonstrated an adhesion strength of .872 kilogram per square centimeter (with a standard deviation of .037). Sample 2 demonstrated a similar adhesion strength of .915 kilogram per square centimeter (with a deviation of 0.038). However, Sample 3 involving dipropylene glycol butyl ether ("DPTB") as the coating material demonstrated a comparatively improved adhesion strength of 1077 kilograms per square centimeter (standard deviation of .026). The following examples are provided for illustration only and are not intended to limit the scope of the invention, as claimed.
Claims (11)
1. A method to modify the properties of concrete that includes: adding to a concrete, mortar or cement mixture, in an amount of 0.05 percent to 10 percent by weight based on the total dry weight of the cement, fibers that have a material of coating which is selected from the group consisting of a glycol ether and a glycerol ether, mixing the resulting mixture to obtain a concrete, mortar or paste mixture in which the individual fibers are homogeneously distributed, and molding the mixture in a; the glycol ether having the formula RO (AO) n-H wherein R comprises an alkyl group of 1 to 7 carbon atoms or a cycloalkyl group of 5 to 7 carbon atoms; A comprises an alkylene group of 3 to 4 carbon atoms; Or is oxygen; n represents an integer from 1 to 10, and H is hydrogen; and the glycerol ether has the formula: CH2- (AO) x-OR? I CH2- (AO) y-OR2 CH2- (AO) Z-0R3 wherein R] _, R2 and R3 are hydrogen or an alkyl group of 1 to 14 carbon atoms, at least one of R] _, R2 and R3 comprises an alkyl group of 1 to 14 carbon atoms; A is a group of 2 to 4 carbon atoms; and x, y and z are integers from 0 to 10. The method of claim 1, wherein the fibers comprise a material that is selected from the group consisting of steel, glass, acrylics and polyolefins. 3. The method of claim 1 wherein the fibers comprise polypropylene. 4. The method of claim 3, wherein the fiber coating material comprises a glycol ether selected from the group consisting of dipropylene glycol-t-butyl ether, di-propylene glycol-n-butyl ether and di-propylene glycol-n-propyl. The method of claim 4, wherein the glycol ether comprises di-propylene glycol-t-butyl ether. The method of claim 4, wherein the fiber coating material comprises glycerol ether having the formula: CH2- (AO) and-OR2 CH2- (AO) z-OR3 wherein R] _, R2 and R3 are hydrogen or an alkyl group of 1 to 14 carbon atoms, at least one of R] _, R2 and R3 comprises an alkyl group of 1 to 14 carbon atoms; A is a group of 2 to 4 carbon atoms; and x, y and z are integers from 0 to 10. The method of claim 6, wherein the glycerol ether is di-t-butylglycerol, and the fibers comprise polypropylene. 8. Coated fibers for modifying the properties of a concrete comprise: a plurality of fibers coated with a material selected from the group consisting of a glycol ether and a glycerol ether; the glycol ether has the formula RO (AO) n-H wherein R comprises an alkyl group of 1 to 7 carbon atoms or a cycloalkyl group of 5 to 7 carbon atoms; A comprises an alkylene group of 3 to 4 carbon atoms; Or is oxygen; n represents an integer from 1 to 10, and H is hydrogen; and the glycerol ether has the formula: CH2- (AO) and-OR2 CH2- (AO) z-OR3 wherein R] _, R2 and R3 are hydrogen or an alkyl group of 1 to 14 carbon atoms, at least one of R] _, R2 and R3 comprises an alkyl group of 1 to 14 carbon atoms; A is a group of 2 to 4 carbon atoms; and x, y and z are integers from 0 to 10. The coated fibers of claim 8, wherein the fiber coating material comprises a glycol ether selected from the group consisting of di-propylene glycol-t-butyl ether. of di-propylene glycol-n-butyl, and di-propylene glycol-n-propyl ether. 10. The coated fibers of claim 9, wherein the fiber comprises polypropylene and the fiber coating material is di-propylene glycol-t-butyl ether. 11. A cementitious composition comprising a hydraulic cementitious binder, water, a fine aggregate and a fiber coated with a material selected from the group consisting of a glycol ether and a glycerol ether; the glycol ether has the formula: RO (AO) n-H wherein R comprises an alkyl group of 1 to 7 carbon atoms or a cycloalkyl group of 5 to 7 carbon atoms; A comprises an alkylene group of 3 to 4 carbon atoms; Or is oxygen; n represents an integer from 1 to 10, and H is hydrogen; and the glycerol ether has the formula: CH2- (AO)? - OR] _ I CH2- (AO) y-OR2 I CH2- (AO) z-OR3 wherein R_, R2 and R3 are hydrogen or an alkyl group of 1 to 14 carbon atoms, at least one of R_, R2 and R3 comprises an alkyl group of 1 to 14 carbon atoms; A is a group of 2 to 4 carbon atoms; and x, y and z are integers from 0 to 10.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08697308 | 1996-08-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA99001679A true MXPA99001679A (en) | 1999-09-20 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5753368A (en) | Fibers having enhanced concrete bonding strength | |
Tagnit-Hamou et al. | Microstructural analysis of the bond mechanism between polyolefin fibers and cement pastes | |
Chand et al. | Effect of self curing chemicals in self compacting mortars | |
EP1799623B1 (en) | Integrally waterproofed concrete | |
Hou et al. | Effect of admixtures in concrete on the corrosion resistance of steel reinforced concrete | |
KR101204872B1 (en) | Ultra-high-performance self-compacting concrete, preparation method thereof and use of same | |
EP0286112B1 (en) | Synthetic fiber suited for use in reinforcing cement mortar or concrete and cement composition containing same | |
US7241338B2 (en) | Sprayable, strain-hardening cementitious compositions | |
Zimbelmann | A method for strengthening the bond between cement stone and aggregates | |
US4878948A (en) | Water resistance additive for cementitious compositions | |
US4902347A (en) | Polyamide fibers, microsilica and Portland cement composites and method for production | |
CA2335056A1 (en) | Air entrainment with polyoxyalkylene copolymers for concrete treated with oxyalkylene sra | |
KR20100020812A (en) | Concrete composition comprising polyamide reinforcing fibers | |
Köksal et al. | Durability properties of concrete reinforced with steel-polypropylene hybrid fibers | |
EP0271825A2 (en) | Hydraulic cementitious compositions reinforced with fibers containing polymerized polyacrylonitrile | |
US4132556A (en) | Reinforced conglomerates for the construction or building industry and process for preparing the same | |
JP2001519318A (en) | Shaped fibers-cement products and reinforcing fibers for such products | |
MXPA99001679A (en) | Fibers having enhanced concrete bonding strength | |
KR102292424B1 (en) | Hybrid fiber-reinforced mortar composition containing steel fiber and carbon fiber, and cement composite with improved flexural performance | |
US20220242790A1 (en) | Non-invasive repair and retrofitting of hardened cementitious materials | |
US7993448B2 (en) | Cement-containing composition for use with alkali-resistant fiberglass and poles made therefrom | |
JP3270443B2 (en) | Cement modifier, cement modification method and modified cement hardened material | |
West et al. | Acrylic-polymer modified GRC | |
Pimienta et al. | Recycled aggregate used for making building blocks | |
JP7312947B2 (en) | Concrete composition and method for producing concrete structure |