NZ616518B2 - 3-mode blended fibers in an engineered cementitious composite - Google Patents
3-mode blended fibers in an engineered cementitious composite Download PDFInfo
- Publication number
- NZ616518B2 NZ616518B2 NZ616518A NZ61651812A NZ616518B2 NZ 616518 B2 NZ616518 B2 NZ 616518B2 NZ 616518 A NZ616518 A NZ 616518A NZ 61651812 A NZ61651812 A NZ 61651812A NZ 616518 B2 NZ616518 B2 NZ 616518B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- fiber
- fibers
- fiber cement
- length
- cellulose fibers
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 262
- 239000011182 bendable concrete Substances 0.000 title description 2
- 239000004568 cement Substances 0.000 claims abstract description 100
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract description 99
- 229920001155 polypropylene Polymers 0.000 claims abstract description 93
- 239000004743 Polypropylene Substances 0.000 claims abstract description 89
- 239000000203 mixture Substances 0.000 claims abstract description 82
- 239000002131 composite material Substances 0.000 claims abstract description 54
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 29
- -1 polypropylene Polymers 0.000 claims abstract description 26
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 17
- 239000002002 slurry Substances 0.000 claims description 17
- 239000003607 modifier Substances 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 230000002209 hydrophobic Effects 0.000 claims description 5
- 238000000151 deposition Methods 0.000 claims description 4
- 230000005660 hydrophilic surface Effects 0.000 claims description 3
- 230000000052 comparative effect Effects 0.000 claims 3
- 238000000034 method Methods 0.000 abstract description 26
- 238000010521 absorption reaction Methods 0.000 abstract description 14
- 229920002678 cellulose Polymers 0.000 abstract description 8
- 239000001913 cellulose Substances 0.000 abstract description 8
- 239000010408 film Substances 0.000 description 13
- 239000010410 layer Substances 0.000 description 11
- 239000004566 building material Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 230000002787 reinforcement Effects 0.000 description 7
- 239000012615 aggregate Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000005755 formation reaction Methods 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 210000001724 Microfibrils Anatomy 0.000 description 4
- 230000001788 irregular Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920000311 Fiber-reinforced composite Polymers 0.000 description 3
- 239000003733 fiber-reinforced composite Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000003014 reinforcing Effects 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L Chromic acid Chemical compound O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- VZJVWSHVAAUDKD-UHFFFAOYSA-N Potassium permanganate Chemical compound [K+].[O-][Mn](=O)(=O)=O VZJVWSHVAAUDKD-UHFFFAOYSA-N 0.000 description 2
- 239000002956 ash Substances 0.000 description 2
- 238000009435 building construction Methods 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 230000002708 enhancing Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- 230000000717 retained Effects 0.000 description 2
- 229910021487 silica fume Inorganic materials 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 240000003917 Bambusa tulda Species 0.000 description 1
- 229960003563 Calcium Carbonate Drugs 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000002918 Fraxinus excelsior Nutrition 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 210000000282 Nails Anatomy 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 210000002381 Plasma Anatomy 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000015450 Tilia cordata Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000004429 atoms Chemical group 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000010882 bottom ash Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004027 cells Anatomy 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000005495 cold plasma Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000004059 degradation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000593 degrading Effects 0.000 description 1
- 230000002939 deleterious Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002349 favourable Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000011068 load Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative Effects 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000000750 progressive Effects 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B28—WORKING CEMENT, CLAY, OR STONE
- B28B—SHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
- B28B1/00—Producing shaped prefabricated articles from the material
- B28B1/52—Producing shaped prefabricated articles from the material specially adapted for producing articles from mixtures containing fibres, e.g. asbestos cement
- B28B1/522—Producing shaped prefabricated articles from the material specially adapted for producing articles from mixtures containing fibres, e.g. asbestos cement for producing multi-layered articles
-
- 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
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
- C04B14/04—Silica-rich materials; Silicates
- C04B14/06—Quartz; Sand
-
- 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
- C04B16/00—Use of organic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of organic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B16/04—Macromolecular compounds
- C04B16/06—Macromolecular compounds fibrous
- C04B16/0616—Macromolecular compounds fibrous from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B16/0625—Polyalkenes, e.g. polyethylene
- C04B16/0633—Polypropylene
-
- 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
- C04B18/00—Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B18/04—Waste materials; Refuse
- C04B18/18—Waste materials; Refuse organic
- C04B18/24—Vegetable refuse, e.g. rice husks, maize-ear refuse; Cellulosic materials, e.g. paper, cork
-
- 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
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/0048—Fibrous materials
- C04B20/0052—Mixtures of fibres of different physical characteristics, e.g. different lengths
-
- 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
- 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
- C04B28/04—Portland cements
-
- 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
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/02—Selection of the hardening environment
- C04B40/024—Steam hardening, e.g. in an autoclave
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A30/00—Adapting or protecting infrastructure or their operation
- Y02A30/30—Adapting or protecting infrastructure or their operation in transportation, e.g. on roads, waterways or railways
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Abstract
Disclosed herein are fiber reinforced cement composite materials incorporating a 3-mode fiber blend that includes cellulose pulp and synthetic fibers in a ratio selected to provide the composite material with improved water absorption characteristics and the same or improved mechanical properties as compared to equivalent composite materials reinforced with predominantly or all cellulose fibers. Also disclosed herein are fiber blends comprised of a combination of cellulose fibers and polypropylene fibers adapted to reinforce cementitious composite articles manufactured by the Hatschek process and autoclave cured. compared to equivalent composite materials reinforced with predominantly or all cellulose fibers. Also disclosed herein are fiber blends comprised of a combination of cellulose fibers and polypropylene fibers adapted to reinforce cementitious composite articles manufactured by the Hatschek process and autoclave cured.
Description
-MODE BLENDED FIBERS IN AN ENGINEERED CEMENTITIOUS
COMPOSITE
CROSS-REFERENCE TO RELATED APPLICATIONS
This application claims the benefit of priority under 35 U.S.C. §119(e)
of U.S. Provisional Application No. 61/485,280 filed on May 12, 2011, which is
incorporated herein by reference in its entirety.
BACKGROUND OF THE INVENTION
Field of the Invention
Embodiments of the present disclosure relate to cementitious
composite materials incorporating reinforcement fibers with improved properties
developed primarily for use in the building and construction industry.
Description of the Related Art
Fiber reinforced cementitious composite materials have been widely
used in building construction. Cellulose fibers, in particular, have been used to reinforce
various fiber cement building products because they impart favorable properties to the
building product. Moreover, cellulose fibers have a unique microstructure with unique
physical and mechanical properties that are suitable for the Hatschek process, the
preferred commercial process for manufacturing fiber cement sheets and panels. For
example, the micro-fibrils in cellulose fibers help to build an effective filtration system to
catch the fine particles in the fiber cement slurry to form a thin fiber-particle film during
the Hatschek process. The micro-fibrils also branch out with the branches functioning as
anchors in the cured fiber cement composite thereby enhancing the bonding at the
interface between the fibers and cementitious matrix.
However, there are also disadvantages associated with using cellulose
fibers to reinforce cementitious building products. For example, the chemical
composition and large surface area of the micro-fibril structure of the cellulose fibers
render the fibers highly hydrophilic. The hydrophilic nature of cellulose fibers can
increase water absorption of the fiber cement composite, which can result in some
performance issues . Furthermore, cellulose fibers are generally more water sensitive and
less alkali resistant. Therefore they can experience progressive degradation over time.
While synthetic fibers have been used to reinforce cementitious
composite materials, prior art products reinforced with synthetic fibers not only require a
much longer manufacturing cycle but also have less than desirable mechanical properties as
compared to products reinforced with cellulose fibers. For example, fiber cement composites
reinforced with synthetic fibers have been typically limited to the air cure process because
synthetic fibers tend to disintegrate at high temperature conditions of the autoclave process that
is commonly used for curing cellulose fiber reinforced cement composites. The air cure
process takes much longer, normally 28 days, as compared to the autoclave cure process, which
usually takes less than 3 days. Replacement of cellulose fibers with synthetic fibers can also
result in lower flexural strength of the fiber cement composite due to the lower fiber-matrix
interface bonding. Moreover, non-cellulose fibers can create added difficulties in
manufacturing using the Hatschek process. Accordingly, there is a need for improved
reinforcement fibers that can impart desirable mechanical properties to cementitious composites
and are also compatible with the Hatschek process and autoclave curing.
[0005a] Any discussion of the prior art throughout the specification should in no way
be considered as an admission that such prior art is widely known or forms part of common
general knowledge in the field.
[0005b] It is an object of the present invention to overcome or ameliorate at least one
of the disadvantages of the prior art, or to provide a useful alternative.
SUMMARY OF THE INVENTION
[0005c] According to a first aspect, the invention provides a fiber cement composite
material, comprising:
about 10% to 80% by weight cementitious binder;
about 20% to 80% by weight silica;
about 0% to 50% by weight density modifier;
about 0% to 10% additives; and
about 0.5% to 20% by weight a 3-mode fiber blend, wherein said fiber blend comprises
short length and high surface area refined cellulose fibers, medium length and medium surface
area unrefined cellulose fibers, and long length and low surface area polypropylene fibers,
wherein the average length of the short length refined cellulose fibers is less than the
average length of the medium length unrefined cellulose fibers and wherein the average length
of the long length polypropylene fibers is greater than the average length of the medium length
unrefined cellulose fibers.
[0005d] According to a second aspect, the invention provides a method of
manufacturing a fiber reinforced cementitious article, comprising:
forming a fiber cement slurry, said fiber cement slurry comprising:
about 10% to 80% by weight cementitious binder;
about 20% to 80% by weight silica;
about 0% to 50% by weight density modifier;
about 0% to 10% additives; and
about 0.5 to 20% by weight a 3-mode fiber blend, wherein said fiber blend comprises
short length and high surface area refined cellulose fibers, medium length and medium surface
area unrefined cellulose fibers, and long length and low surface area synthetic polypropylene
fibers,
wherein the average length of the short length refined cellulose fibers is less than the
average length of the medium length unrefined cellulose fibers and wherein the average length
of the long length polypropylene fibers is greater than the average length of the medium length
unrefined cellulose fibers,
depositing said fiber cement slurry on a plurality of sieve cylinders that are rotated
through the fiber cement slurry, wherein the cellulose fibers and polypropylene fibers filter the
fiber cement slurry to form a thin fiber cement film;
transferring a series of sequential layers of the thin fiber cement films to a belt so as to
build a thicker fiber cement layer;
removing water from the thicker fiber cement layer; and
curing said thicker fiber cement layer in an autoclave at a temperature of at least 150°C.
[0005e] According to a third aspect, the invention provides a fiber reinforced
cementitious article when produced by the method according to the second aspect.
[0005f] Unless the context clearly requires otherwise, throughout the description and
the claims, the words “comprise”, “comprising”, and the like are to be construed in an inclusive
sense as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including,
but not limited to”.
The compositions, materials, articles, and methods of manufacture of this
disclosure each have several aspects, no single one of which is solely responsible for its
desirable attributes.
Any terms not directly defined herein shall be understood to have all of the
meanings commonly associated with them as understood within the art. Certain terms are
discussed below, or elsewhere in the specification, to provide additional guidance to the
practitioner in describing the compositions, methods, systems, and the like of various
embodiments, and how to make or use them. It will be appreciated that the same thing may be
said in more than one way. Consequently, alternative language and synonyms may be used for
any one or more of the terms discussed herein. No significance is to be placed upon whether or
not a term is elaborated or discussed herein. Some synonyms or substitutable methods,
materials and the like are provided. Recital of one or a few synonyms or equivalents does not
exclude use of other synonyms or equivalents, unless it is explicitly stated. Use of examples in
the specification, including examples of terms, is for illustrative purposes only and does not
limit the scope and meaning of the embodiments herein.
One embodiment of the present disclosure provides a fiber cement composite
material incorporating a novel fiber blend (3-mode blend) adapted to reinforce and improve the
mechanical properties of the composite material. The fiber cement
composite material includes about 10%-80% by weight cementitious binder, about 20%-
80% by weight silica, about 0% - 50% by weight density modifier, about 0%-10%
additives, and about 0.5%-20% by weight a 3-mode fiber blend that includes refined
cellulose fiber, unrefined cellulose fiber and synthetic fibers. The refined cellulose fiber
is normally shorter with a length of 0.8 to 2.0 mm and high surface areas. The unrefined
cellulose fiber has a length of 1.5 to 3.0 mm with medium surface areas. The synthic fiber
has longer fibers and lowest surface areas. The refined cellulose fiber accounts for 50 to
75% of the total fiber mass or population. The unrefined cellulose fiber accounts for 10 to
% of the total fiber mass or population while the synthetic fiber is about 10 to 25% of
total fiber mass or population. In one implementation, the ratio of cellulose fibers to
synthetic fibers in the fiber blend is between 3 and 24, more preferably between 4 to 12.
In another implementation, the synthetic fibers comprise polypropylene (PP) fibers. In
another implementation, the synthetic fibers consist essentially of PP fibers. The PP
fibers are preferably fibrillated with irregular forms. In some implementations, the PP
fibers have an average length of between 4 to 15 millimeters (mm), preferably 6 to 12
mm In some other implementations, the fiber cement composite material comprises
about 3% to 10% by weight cellulose fibers and about 0.25% to 2% by weight PP fibers,
or preferably 0.5% to 1.5% by weight PP fibers.
In other implementations, the fiber blend includes three modes of fiber
length distribution. One mode can comprise refined shorter cellulose fibers. A second
mode can comprise unrefined cellulose fibers. A third mode can comprise long PP fibers.
Preferably, the average length of the refined shorter cellulose fibers is less than the
average length of the unrefined cellulose fibers; and the average length of the PP fibers is
longer than the average length of the unrefined cellulose fibers. In one implementation,
one mode can comprise about 50% to 80% refined shorter cellulose fibers having an
average length of less than or equal to 2 mm. A second mode can comprise about 10% to
% unrefined cellulose fibers having an average length of greater than or equal to 2 mm,
preferably between 2 mm to 2.5 mm. A third mode can comprise about 10% to 25%
long PP fibers having an average length of between 4 mm to 15 mm. In yet some other
implementations, the PP fibers are engineered with a hydrophilic surface and a
hydrophobic bulk part to form fiber cement grade PP fibers. In one embodiment, the
fiber reinforced composite materials preferably has a moisture movement (MM) of less
than 0.5%. In another embodiment, the material have a moisture movement of at least
% less than that of an equivalent fiber cement material.
Another embodiment of the present disclosure provides a fiber
reinforced cement composition comprising a hydraulic binder, aggregates, cellulose
fibers, and polypropylene fibers. Preferably, the polypropylene fibers have irregular
forms. In one implementation, the ratio of the weight percent of cellulose fibers to
polypropylene fibers is between 3 to 24, preferably between 4 to 12. In another
implementation, the composition comprises about 2% to 10% by weight cellulose fibers
and about 0.25% to 2% by weight polypropylene fibers. In another implementation, the
fiber reinforced cement composition is adapted for forming exterior wall sidings.
Yet another embodiment of the present disclosure provides a method of
manufacturing a fiber reinforced cementitious article suitable for the hatschek process and
autoclave curing. The method includes the steps of forming a fiber cement slurry which can
comprise a hydraulic binder, aggregates, water, cellulose fibers and polypropylene fibers;
depositing the fiber cement slurry on a plurality of sieve cylinders that are rotated through the
fiber cement slurry wherein the cellulose fibers and polypropylene fibers filter the fiber cement
slurry to form a thin fiber cement film. The method further includes the steps of transferring a
series of sequential layers of the thin fiber cement films to a felt so as to build a thicker fiber
cement layer; removing water from the thicker fiber cement layer; transferring and winding the
fiber cement layer onto a size roller to achieve desired final thickness; cutting and unwinding fiber
cement sheet onto a conveyor; and curing the fiber cement sheet in an autoclave at a temperature
of at least 150° c. In some implementations, the method further includes the step of forming the
autoclave cured fiber cement sheet into a building construction panel.
BRIEF DESCRIPTION OF THE DRAWINGS
FIGURES 1A-1B are photos of two different types of synthetic fibers
after the Parr bomb test according to certain embodiments of the present disclosure.
FIGURES 2A-2B are photos illustrating examples of synthetic fibers
in a cement matrix according to certain preferred embodiments before the autoclave cycle
under a microscope.
FIGURES 3A-3C are various views of the synthetic fiber shown in
FIGURES 2A-2B in the fiber composite matrix.
FIGURE 4 is a chart showing the moisture movement of various fiber
cement composite material samples made in accordance with certain preferred
embodiments as compared to controls.
FIGURE 5 is a chart showing the water absorption values of fiber
cement composite material samples made in accordance with certain preferred
embodiments compared to the control formulation.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Disclosed herein are fiber cement articles reinforced with a fiber blend
pre-selected to provide the fiber cement articles with improved mechanical and/or
chemical physical properties. Also disclosed herein are fiber blends comprised of
synthetic and natural fibers at pre-selected ratios for reinforcing cementitious composite
materials and methods for manufacturing. Also disclosed herein are synthetic and
cellulose fiber blends adapted to reinforce cementitious composite articles manufactured
by the Hatschek process and autoclave cured. Also disclosed herein are fiber reinforced
cement formulations that include cellulose pulp and synthetic fibers in a ratio selected to
provide a building material with improved water absorption characteristics and the same
or improved mechanical properties as compared to equivalent building materials
reinforced with predominantly or all cellulose fibers.
One of the challenges in incorporating synthetic reinforcing fibers,
such as polypropylene (PP) fibers, in fiber cement composite materials is that synthetic
fibers, unlike cellulose fibers, are not configured to catch sufficient amount of fine
particles in fiber cement slurry to form a thin fiber cement film during the Hatschek
process. Additionally, most synthetic fibers like PP fibers will disintegrate at elevated
autoclave temperatures. As such, while synthetic fibers have been incorporated in fiber
cement articles, the synthetic fibers are not successfully added in sufficient quantities as a
substitute for substantial amounts of cellulose fibers, especially not in fiber cement panels
and sheets that are typically manufactured by the Hatschek process and autoclave cured.
The inventors have developed certain fiber reinforced composite material compositions
that incorporate fiber blends comprising synthetic and cellulose fibers selected to
reinforce cementitious articles manufactured by the Hatschek process and cured at
elevated autoclave temperatures without deleterious effects.
Fiber Blends
Various embodiments of the present disclosure provide novel 3-mode
blends of synthetic and cellulose fibers that can be incorporated in a cementitious
composition for reinforcing composite materials formed by the Hatschek process and
cured at elevated autoclave temperatures. In certain preferred embodiments, the synthetic
fibers include polypropylene (PP) fibers that are engineered with certain properties. In
one embodiment, the PP fibers have a high degree of crystallinity, high linear density, and
high thermal resistance. In some implementations, the PP fibers have a linear density of at
least 2.2 + 0.22 dtex and a high thermal resistance. In one embodiment, the PP fibers are
engineered to have a high melting point and narrow molecular weight distribution to
survive the high temperatures. In some implementations, the PP fibers have length of
between 4 to 15 millimeters (mm), preferably between 6 to 10 mm of mono-filaments in
some embodiments. The PP fibers can be mono-filament or fibrillated with different
shapes, including circular or irregular forms. The cross-section of the PP fibers can have
eccentric sheath core or concentric sheath core, hollow splittable, zigzag, wavy, or spiral
types. The irregular shapes can help for improving the mechanical interlocking bonding
to resist fracture of the fiber cement. The irregularity of the PP fiber surface of various
preferred embodiments will help the PP fibers to be caught on the filter drum for film
formation during the Hatschek process.
To improve the affinity between PP fibers and cement, the PP fibers of
some embodiments of the present disclosure may be modified to have a hydrophilic
surface while leaving the bulk part of PP fiber hydrophobic to produce a fiber cement
grade PP fiber. In some embodiments, the PP fiber surface is made hydrophilic by first
chemically altering the fiber surface layer and followed by depositing an extraneous layer
on top of the altered fiber surface layer, thereby generating a sharp interface. Given the
non-reactive character of the PP fiber surface, the PP fibers require generating high
energy species, such as radicals, ions, molecules in excited electronic states, etc. Coating
physical treatment involves itself in the generation, usually by high-energy methods, of
matter fundamentals, such as atoms or atomic clusters, to be deposited on material
surfaces. Such treatments for modification include flame, corona, cold plasma, hot
plasma, UV, laser, electron beam, ion beam, and sputtering. Impregnation of PP fiber
with surfactants is an example of the additional layer on the PP fibers surface.
In some embodiments, the PP fiber surface is made hydrophilic by wet
treatment such as covalent attachment of polymer chains. Wet treatment may include
exposing the PP fiber surface to oxidizing wet chemicals such as chromic acid, nitric acid
or potassium permanganate to result in general oxidation, forming carbonyl groups,
hydroxyl groups and carboxylic acid groups on the polymer surface. The covalent
attachment of polymer chains to the PP fiber surface can be achieved by either graft
polymerization or polymer grafting after the pretreatment with UV, electron beam, and g -
ray irradiation.
The PP fibers of preferred embodiments can be supplied in a bundle
form. Appropriate dosing and mixing procedures and equipment can be used to ensure
proper dispersion of the fibers, although the surface of the fibers may have been modified
to be hydrophilic.
The PP fibers are preferably blended with cellulose fibers at
preselected ratios for optimum performance. In one embodiment, the percent by weight
ratio of PP fibers to cellulose fibers in a fiber cement composition is between 3 to 24, or
between 4 to 12. The cellulose fibers preferably have a length between 0.5 to 3mm. The
micro-fibril structures in the cellulose fibers are suitable for filtration process, which in
turn are good for film formation on the filter drum in a Hatschek process. PP fibers in
monofilament form have poor capability of catching fine particles from film formation.
Well blended PP fibers and cellulose fibers according to preferred embodiments of the
present disclosure will build an inter-penetration fiber network, which in turn provides
good film formation in the Hatschek process.
Figure 1A is a photo showing high crystalline PP fibers according one
embodiment of the present disclosure. Figure IB is a photo showing a general
commercial PP fiber. The PP fibers in both Figures 1A and IB are shown after the Parr
bomb test, which simulates elevated autoclave curing condition for the fiber cement
materials. The bomb cell (part No at 4744 with total capacity at 45 ml) is from Parr
Instrument Company. Weight at 0.5 grams of synthetic fiber is put in the PTFE cup with
pre-filled 25 ml of water with pH at 13. The synthetic fiber is submerged inside the water,
which may float onto the water top surface. The PTFE cover is put back and sealed inside
the bomb body. The bomb with sample is put in the oven at 160C and left inside for 15
hrs before cooling down to room temperature. The bomb body is opened for fiber damage
study under microscopy after cooling down to room temperature. The high crystalline PP
fibers still retained good fiber integrity while the commercial PP fibers broke into pieces
and slightly melted together. Thus, the high crystalline PP fibers can survive the
autoclave for the short hydration process time with increased temperatures.
In some embodiments, the fiber blend comprises three modes of fibers.
The fiber blend includes a combination of refined shorter cellulose fibers, preferably
between 0.8 mm to 2 mm with highest surface areas; unrefined cellulose fibers,
preferably between 2 mm to 2.5mm with medium surface areas; and long PP fibers,
preferably between 4 mm to 15 mm with lowest surface areas. The combination of the
three modes of fibers helps to achieve balanced product performance in Modulus of
Rupture (MOR),toughness and nailablity. In some implementations, the fiber blend
comprises about 50 to 80 % refined shorter cellulose fibers, about 10 to 25 % unrefined
cellulose fibers, and about 10 to 25 % long PP fibers.
Fiber Cement Compositions
One preferred composition of the fiber reinforced composite material
comprises a cementitious binder, aggregates, optional density modifier, optional various
additives, and a fiber blend comprising cellulose fibers and PP fibers adapted to improve
various material properties. It will be appreciated that not all of these components are
necessary to formulate a suitable building product, and thus, in certain embodiments, the
formulation may simply comprise cementitious binder and blended fibers.
The cementitious binder is preferably Portland cement but can also be,
but is not limited to, high alumina cement, lime, high phosphate cement, and ground
granulated blast furnace slag cement, or mixtures thereof. The aggregate is preferably
ground silica sand but can also be, but is not limited to, amorphous silica, micro-silica,
diatomaceous earth, coal combustion fly and bottom ash, rice hull ash, blast furnace slag,
steel slag, mineral oxides, mineral hydroxides, clays, magnasite or dolomite, metal oxides
and hydroxides, and polymeric beads, or mixtures thereof.
The density modifiers can be organic and/or inorganic lightweight
materials with a density less than 1.5 g/cm . The density modifiers may include plastic
materials, glass and ceramic materials, calcium silicate hydrates, microspheres, and
volcanic ashes, including perlite, pumice, shirasu basalt, and zeolites in expanded forms.
The density modifiers can be natural or synthetic materials.
The additives can include, but are not limited to, viscosity modifiers,
fire retardants, waterproofing agents, silica fume, geothermal silica, thickeners, pigments,
colorants, plasticizers, dispersants, forming agents, flocculents, drainage aids, wet and dry
strength aids, silicone materials, aluminum powder, clay, kaolin, alumina trihydrate,
mica, metakaolin, calcium carbonate, wollastonite, and polymeric resin emulsion, and
mixtures of thereof or other materials.
The cellulose fibers in the fiber blend can be unrefined/unfibrillated or
refined/fibrillated cellulose pulps from various sources, including but not limited to
bleached, unbleached, semi-bleached cellulose pulp. The cellulose pulp can be made of
softwood, hardwood, agricultural raw materials, recycled waste paper or any other forms
of lignocellulosic materials. Cellulose fibers can be made by various pulping methods. In
the pulping process wood or other lingocellulosic raw materials such as kenaf, straw, and
bamboo are reduced to a fibrous mass by the means of rupturing the bonds within the
structure of lignocellulosic materials. This task can be accomplished chemically,
mechanically, thermally, biologically, or by combinations of these treatments.
The synthetic fibers in the fiber blend can be of any type including, but
not limited to, glass fibers, polyester, polypropylene, aromatic polyamide, and acrylic
fibers. These types of fibers can be made to be used in a composite product that is air
cured or treated in such a way as to be able to survive a higher temperature autoclave
cycle. An example of such a fiber can be found as described in US Patent 6,010,786
(Takai).
In one embodiment, the fiber cement composition comprises about
%-80% by weight cementitious binder; about 20%-80% by weight silica (aggregates);
about 0%-50% by weight density modifier; about 0%-10% by weight additives; and about
0.5%-20% by weight of fiber blend comprising cellulose fibers and PP fibers. In one
implementation, the fiber cement formulation comprises about 4.5% - 9% fiber blend. In
another implementation, the fiber blend comprises 3%-10% cellulose fibers, or preferably
4%-8% cellulose fibers based on total mass of dry mix.
In another embodiment, which is particularly suitable for autoclave
curing, the formulation comprises about 20%-50% cement; about 30%-70% ground
silica; about 0%-50% density modifiers; about 0%-10% additives; and about 2%-10%
fiber blend comprising cellulose fibers and PP fibers.
Substitution of Cellulose Fibers with Preselected PP Fibers
Certain preferred embodiments of the present disclosure are directed to
substituting a fraction of the cellulose fibers in a fiber cement composition with PP fibers,
preferably fiber cement grade PP fibers, to reduce the moisture absorption of the resulting
product without detrimentally affecting other properties. In one embodiment, up to 50%
of cellulose fibers in a fiber cement composition can be substituted with fiber cement
grade PP fibers. In some implementations, the fiber cement composition includes 0.5% or
more hydrophobic polypropylene (PP) fibers as well. The fiber blend will provide the
balanced benefits of cellulose and PP fibers in which cellulose fibers serve as processing
aids, density modifier and reinforcement, while PP fibers are used as the secondary
reinforcement to enhance the toughness. The water sensitivity of the formed composite
will be significantly reduced.
In some embodiments, by replacing up to about 50% of the cellulose
fibers with variable lengths distributed between 0.8-3.0 mm with the addition of a small
amount of hydrophobic PP fibers, the hydrophilic property of the fiber cement slurry and
composites can be significantly reduced while the film formation capability in the
Hatschek process is still maintained. The long term performance or reinforcement of the
blended (PP and cellulose fibers) fiber cement composite is retained by the stability of the
PP fibers. The length of the PP fibers can be engineered to suit different reinforcement
requirements. For example, shorter and high surface area fibers may improve strength of
the composite, while longer fibers can make the composite more ductile
Figures 2A and 2B are photos taken under polarized light of a fiber
blend incorporated in a cementitious formulation according to certain preferred
embodiments of the present disclosure. The fiber blend comprises fiber cement grade PP
fibers and cellulose fiber. As shown in Figures 2A and 2B, the mixture of PP and
cellulose fiber was dispersed very well within the inter-network structure.
Figures 3A-3C are photos showing a fiber cement composition
reinforced with a fiber blend according to one embodiment after elevated autoclave
curing. The fiber blend comprises a mixture of PP fibers and cellulose fibers. As shown
in Figure 3A, the PP fibers remain fully intact after autoclave curing. Figure 3C shows
that upon sample breaking, the PP fibers did not break and pulled out on the sample
matrix surface, which is different from that of cellulose fibers as shown in the photo in
Fig. 3B. This observation is consistent with the fact that PP fiber is more ductile than that
of cellulose. Moisture movement (MM) in the preferred embodiments has shown a
surprising reduction compared to control samples in post carbonation measure. After
carbonation, samples were tested and the moisture movement was reduced to a level that
showed vast improvements over the control samplesFigure 4 shows the moisture
movement for the present disclosure in samples (3-6) and the controls (1-2). Samples (3-
6) were made in accordance with the fiber cement formulations disclosed herein. As
shown, samples made according to the preferred embodiments had less moisture
movement than the control samples, with the improvement of up to about 21%. The
reduction in moisture movement can inhibit propagation of joint spacing and cracking
around nails when the products are in service.
Water absorption coefficient (WAC) is also shown to be significantly
reduced in the preferred embodiments. Figure 5 shows the water absorption coefficient
for the samples (5-6) and the control (1). As shown, there is about 41% improvement for
the invention samples over the control. The lower water absorption values lead to a more
durable fiber cement product. It has been found that a decrease in water absorption
properties transfers into better performance in freeze thaw and shrinkage of the building
material. The WAC test method is based on ISO 15148:2002(E). Cellulose pulp was
tested at from 4 to 6% and the polypropylene fiber was tested at from 0.25 to 1.5% in
various combinations. On the lower end of the fiber combinations, 0.25-0.50% PP fiber
with 4.5% cellulose fiber did not provide enough reinforcement in the form of strain
property. On the upper end of using 1.5% PP fiber and 6% cellulose fiber, it was found
that the water absorption improvements did not further improve while the cost increased
significantly. It was found that at least 5% cellulose fiber is needed to achieve the
required strain to form a durable product. The initial screenings of a filter pad
formulations showed similar results to the properties and characteristics of the scaled up
Hatschek process formulations that led to the final blend of fibers that provided a
composite product that was comparable to an all cellulose fiber composite product.
With an overall total reduction in fiber content, and more specifically
cellulose fibers, it has been found that water absorption and moisture movement
properties have improved leading to increased overall durability of the fiber cement
composite. The 3-mode blended fiber composite maintains many of its physical properties
as well and provides increased drainage on the process side which makes the Hatschek
machine run faster and with less load. While density is increased slightly due to
reduction of fiber content, nailability and strength of the product are acceptable for
installation. No predrilling is required of the blended composite product.
Moisture movement (MM) in the preferred embodiments has shown a
surprising reduction compared to control samples in post carbonation measure. After
carbonation, samples were tested and the moisture movement was reduced to a level that
showed vast improvements over the control samples. In Figure 4, it can be seen that the
reduction in moisture movement in Examples 1, 2, 3, and 4 of the blended composites
compared to the control samples.
Other preferable formulations can be seen in the Examples in Table 1
below.
TABLE 1: Summary of Properties
Example MOR Density WAC (back) MM % Nailability
Mpa g/cc kg/m *sec 0.5*1000
1 Par Par Excellent
.08 0.58
(Control)
2(Control) Par Par 17,63 0.51 Excellent
Better Higher 14.44 Excellent
3 0.48
4 Better Higher 12.05 0.49 Very Good
Par Higher 5.91 0.46 Very Good
6 Better Higher 6.04 0.48 Very Good
TABLE 2: Summary of Properties I
Example MOR Density WAC (back) MM % Nailability
kg/m *sec 0.5*1000
Mpa g/cc
1 Par Par 10.08 0.58 Excellent
(Control)
Par Higher 5.91 0.46 Very Good
6 Better Higher 6.04 0.48 Very Good
TABLE 3: Summary of Properties II
Example MOR Density WAC (back) MM % Nailability
Mpa g/cc kg/m2*sec 0.5*1000
2 (Control) Par Par 17.63 0.51 Excellent
3 Better Higher 14.44 0.48 Excellent
4 Better Higher 12.05 0.49 Very Good
Density of the blended composites has shown an increase as can be
seen in Tables 2 and 3 above. Table 2 shows formulation examples with a lower density
modifier while Table 3 shows formulations that do not contain a density modifier. The
nailing test results provided values that were comparable to the control samples. The
mechanical properties show durability of the product and installation soundness that
provide a composite that can replace current fiber cement products at a reduced raw
material cost while not suffering a decline in performance. The MOR, density, and MM
tests were done according to ASTM CI 186.
Water absorption coefficient (WAC) is also shown to be significantly
reduced in the preferred embodiments. Figure 5 indicates water absorption rates of two
composite examples, 5 and 6. It has been found that a decrease in water absorption
properties influence better performance in freeze thaw and shrinkage of the building
material. The WAC test method is based on ISO 15148:2002(E).
The preferred embodiment also improves the smoothness of the product by more
than 15%.
Various preferred embodiments of the present disclosure provide fiber
cement building materials with improved Modulus of Rupture (MOR), acceptable density
range and lower moisture movement (MM) with comparable performance in other
criteria. In one embodiment, the fiber cement building material has improved resistance
to freeze and thaw and improved dimensional stability compared to the materials made
with 100% cellulose fibers, for example using 7-10% pulp content, as well as other
property enhancements, while maintaining the mechanical and physical properties such as
nailability. This achievement was unexpected as the brittleness of a higher cement
containing composite was thought to hinder nailing capabilities.
Some embodiments of the present disclosure are directed to
manufacture a new building material that contains a blend of cellulose fibers and
polypropylene fibers at preselected ratios. The formulation can be used to produce fiber-
reinforced cement composites with the Hatschek manufacturing process. In the Hatschek
process, a diluted aqueous suspension is filled in the tub fitted with means for uniformly
distributing constituents within the tubs. A filter drum is partially immersed in each tub
and the rotation makes the deposition on the drum surface to build up the thin film layer
composed of fibers, aggregates, hydraulic binders and additives. The film is carried by a
felt onto a size roller, where the film thickness is built up. It is then cut to unwind from
the size roll and one sheet of fiber cement is formed. The fiber cement sheet can be
subsequently cured at a temperature up to 175°C autoclave, preferably 160°C and a
pressure of about 75 psi without degrading the fibers.
The embodiments illustrated and described above are provided as
examples of certain preferred embodiments of the present invention. Various changes and
modifications can be made from embodiments presented herein by those skilled in the art
without departure from the spirit and scope of this invention.
Claims (12)
1. A fiber cement composite material, comprising: about 10% to 80% by weight cementitious binder; about 20% to 80% by weight silica; about 0% to 50% by weight density modifier; about 0% to 10% additives; and about 0.5% to 20% by weight a 3-mode fiber blend, wherein said fiber blend comprises short length and high surface area refined cellulose fibers, medium length and medium surface area unrefined cellulose fibers, and long length and low surface area polypropylene fibers, wherein the average length of the short length refined cellulose fibers is less than the average length of the medium length unrefined cellulose fibers and wherein the average length of the long length polypropylene fibers is greater than the average length of the medium length unrefined cellulose fibers.
2. The fiber cement composite material according to claim 1, wherein the polypropylene fibers have an average length of between 4 mm and 15 mm.
3. The fiber cement composite material according to claim 1 or claim 2, wherein the polypropylene fibers are engineered with a hydrophilic surface and a hydrophobic bulk part.
4. The fiber cement composite material according to any one of the preceding Claims, wherein the percent by weight ratio of the cellulose fibers to the synthetic fibers is between 3 to
5. The fiber cement composite material according to any one of the preceding claims, wherein the fiber blend comprises about 50% to 80% of the total fiber mass short length refined cellulose fibers having an average length of less than or equal to 2 mm, about 10% to 25% of the total fiber mass medium length unrefined cellulose fibers having an average length of between 2 to 3 mm, and about 10 to 25 % of the total fiber mass long length polypropylene fibers having an average length between 4 to 15 mm.
6. The fiber cement composite material according to any one of the preceding claims, wherein said material having a moisture movement (MM) of less than 0.5%.
7. The fiber cement composite material according to any one of the preceding claims 1 to 5, wherein the moisture movement of the composite material is at least 25% less than that of an equivalent fiber cement composite material containing no synthetic fibers.
8. A method of manufacturing a fiber reinforced cementitious article, comprising: forming a fiber cement slurry, said fiber cement slurry comprising: about 10% to 80% by weight cementitious binder; about 20% to 80% by weight silica; about 0% to 50% by weight density modifier; about 0% to 10% additives; and about 0.5 to 20% by weight a 3-mode fiber blend, wherein said fiber blend comprises short length and high surface area refined cellulose fibers, medium length and medium surface area unrefined cellulose fibers, and long length and low surface area synthetic polypropylene fibers, wherein the average length of the short length refined cellulose fibers is less than the average length of the medium length unrefined cellulose fibers and wherein the average length of the long length polypropylene fibers is greater than the average length of the medium length unrefined cellulose fibers, depositing said fiber cement slurry on a plurality of sieve cylinders that are rotated through the fiber cement slurry, wherein the cellulose fibers and polypropylene fibers filter the fiber cement slurry to form a thin fiber cement film; transferring a series of sequential layers of the thin fiber cement films to a belt so as to build a thicker fiber cement layer; removing water from the thicker fiber cement layer; and curing said thicker fiber cement layer in an autoclave at a temperature of at least 150°C.
9. A fiber reinforced cementitious article when produced by the method according to claim
10. A fiber cement composite material substantially as herein described with reference to any one of the embodiments of the invention illustrated in the accompanying drawings and/or examples, or part thereof, but excluding comparative examples.
11. A method of manufacturing a fiber reinforced cementitious article substantially as herein described with reference to any one of the embodiments of the invention illustrated in the accompanying drawings and/or examples, or part thereof, but excluding comparative examples.
12. A fiber reinforced cementitious article substantially as herein described with reference to any one of the embodiments of the invention illustrated in the accompanying drawings and/or examples, or part thereof, but excluding comparative examples.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161485280P | 2011-05-12 | 2011-05-12 | |
US61/485,280 | 2011-05-12 | ||
PCT/US2012/037641 WO2012155103A1 (en) | 2011-05-12 | 2012-05-11 | 3-mode blended fibers in an engineered cementitious composite |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ616518A NZ616518A (en) | 2015-11-27 |
NZ616518B2 true NZ616518B2 (en) | 2016-03-01 |
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