WO2014022891A1 - Cementitious copolymer composition - Google Patents

Cementitious copolymer composition Download PDF

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Publication number
WO2014022891A1
WO2014022891A1 PCT/AU2013/000878 AU2013000878W WO2014022891A1 WO 2014022891 A1 WO2014022891 A1 WO 2014022891A1 AU 2013000878 W AU2013000878 W AU 2013000878W WO 2014022891 A1 WO2014022891 A1 WO 2014022891A1
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WO
WIPO (PCT)
Prior art keywords
cementitious
copolymer composition
copolymer
coating
coats
Prior art date
Application number
PCT/AU2013/000878
Other languages
French (fr)
Inventor
Stephen Maxwell PAPA
Gregory George REYNOLDS
Original Assignee
Papa Stephen Maxwell
Reynolds Gregory George
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2012903414A external-priority patent/AU2012903414A0/en
Application filed by Papa Stephen Maxwell, Reynolds Gregory George filed Critical Papa Stephen Maxwell
Publication of WO2014022891A1 publication Critical patent/WO2014022891A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B26/00Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
    • C04B26/02Macromolecular compounds
    • C04B26/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions 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
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00482Coating or impregnation materials
    • C04B2111/00525Coating or impregnation materials for metallic surfaces
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/0075Uses not provided for elsewhere in C04B2111/00 for road construction
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Definitions

  • the present invention is directed towards a cementitious copolymer composition and a method for it use in the construction or repair of roads.
  • road compositions are prepared from aggregate compositions of asphalt (bitumen) and rock, wherein the asphalt is utilised as a binder in order to create a hardened product which is laid over a rock or cement foundation.
  • Asphalt pavement material is commonly composed of 5% asphalt cement and 95% aggregates (stone, sand, and gravel). Due to its highly viscous nature, asphalt cement must be heated so it can be mixed with the aggregates and spread across the intended surface.
  • U.S. Pat. No. 4, 145,322 discloses a process for preparing a bitumen-polymer composition consisting of mixing a bitumen, with a block copolymer, having an average molecular weight between 30,000 and 300,000.
  • the colpolymer has the theoretical formula S x B y , in which S corresponds to styrene structure groups and B corresponds to conjugated diene structure groups, and x and y are integers.
  • the resulting bitumen- polymer composition is used for road-coating, industrial coating, or other industrial applications. Whilst it remains that the majority of the physical properties of the resulting road composition are increased, they remain un-useful for the purposes of road compositions, mainly due to increased viscosity of the resulting product, where separation of the asphalt and polymer may occur.
  • the present invention seeks to overcome, or at least ameliorate, one or more of the deficiencies of the prior art mentioned above, or to provide the consumer with a useful or commercial choice.
  • [001 1 ] Those skilled in the art will appreciate that the invention described herein is susceptible to variations and modifications other than those specifically described. The invention includes all such variation and modifications. The invention also includes all of the steps, features, formulations and compounds referred to or indicated in the specification, individually or collectively and any and all combinations or any two or more of the steps or features.
  • copolymer mixture will be understood to be a polymerised composition of two or more monomeric species.
  • a cementitious copolymer composition comprising:
  • the composition may include other components, thus the total volume percentage of the above components may not equal 100 percent. At times when the cementitious copolymer composition comprises only the above components, their total volume percentage will equal 100 percent.
  • the cementitious additive comprises a Portland cement.
  • the cementitious additive comprises a blended cement
  • the cementitious additive comprises:
  • the cementitious additive may include other components, thus the total volume percentage of the above components may not equal 100 percent. At times when the cementitious additive comprises only the above components, their total volume percentage will equal 100 percent
  • the copolymer mixture may be provided as a resin
  • the copolymer mixture may be provided as a powdered solid.
  • the copolymer consists one or more ethylenically unsaturated monomers.
  • the ethylenically unsaturated monomers are selected from the group consisting of vinyl esters, vinyl acetate methacrylates, methacrylic acid esters, vinylaromatics, olefins, 1 ,3-dienes and vinyl halides and optionally further monomers copolymerizable therewith.
  • Suitable monomers from the group of vinyl esters are, for example, those of carboxylic acids having 1 to 15 carbon atoms.
  • the monomer is selected from the group containing vinyl acetate, vinyl propionate, vinyl butyrate, vinyl 2- ethylhexanoate, vinyl laurate, 1 -methylvinyl acetate, vinyl pivalate and vinyl esters of branched monocarboxylic acids having 9 to 1 1 carbon atoms.
  • Suitable monomers from the group of methacrylic acid esters are, for example methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, n-butyl acrylate, n-butyl methacrylate, t-butyl methacrylate, t- butyl methacrylate, 2-ethylhexyl acrylate.
  • Particularly preferred are methyl methacrylate, methyl acrylate, n-butyl methacrylate, t-butyl acrylate or 2-ethylhexyl acrylate.
  • Suitable monomers from the group of vinylaromatics are styrene, methyl styrene or vinyl toluenenyl.
  • a suitable monomer from the group of vinyl halides is vinyl chloride.
  • Suitable monomers from the group of olefins are ethylene, propylene, and the preferred dienes are 1 ,3-butadiene and isoprene.
  • the copolymer mixture is copolymer of one or more ninyl ester and ethylene. Still preferably the copolymer mixture is a vinyl acetate ethylene (VAE) resin.
  • VAE vinyl acetate ethylene
  • the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 99 to 75%, wherein the remainder of the content comprises ethylene.
  • the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 80 to 92%, wherein the remainder of the content comprises ethylene.
  • the copolymer mixture comprises 86% vinyl acetate and 14% ethylene.
  • two or more vinyl acetate ethylene dispersions of varying monomer ratios are combined to provide the copolymer mixture.
  • the aqueous solution is water.
  • the composition further comprises a pest control additive.
  • the composition is adapted for application by a spray applicator, brush or roller.
  • the viscosity of the cementitious copolymer composition may be controlled by the amount of aqueous solution in the composition.
  • a method for coating a surface comprising the steps of: preparing the surface; and applying one or more coats of the cementitious copolymer composition of the invention to the surface.
  • the surface may be bitumen, asphalt, concrete, compacted ground, graded ground, embankments, tailings dams, bunds for mines, or steel.
  • the surface is trafficable.
  • the preparation of the surface comprises cleaning the surface. More preferably, the cleaning of the surface removes dirt, debris and/or any oils on the surface.
  • the application of the cementitious copolymer composition is by way of a spray applicator, a roller or a brush.
  • cementitious copolymer composition Preferably, two coats of the cementitious copolymer composition are applied to the surface. Preferably still, three coats of the cementitious copolymer composition are applied to the surface. [0041 ] In one form of the present invention, a layer of gravel is applied between layers of the cementitious copolymer composition.
  • the surface is a bitumen or concrete road.
  • the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 1 and 15 mm.
  • the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 5 and 13 mm.
  • the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 8 and 12 mm.
  • the method for coating of a surface may be used to coat steel structures in order to provide additional strength and water
  • the method for coating of a surface may be used to line the insides of shipping containers, in order to provide additional strength, provide rust resistance and waterproofing.
  • a method for the repair of damaged road surfaces comprising the steps of: preparing the damaged road surface; and applying one or more coats of a cementitious copolymer composition of the invention to the damaged road surface.
  • the preparation of the damaged road surface comprises cleaning the surface.
  • the cleaning of the damaged surface removes dirt, debris and/or any oils on the surface.
  • copolymer composition is applied to the damaged road surface through a spray applicator, a roller or a brush.
  • a spray applicator Preferably, two coats of the cementitious copolymer composition are applied to the damaged road surface.
  • three coats of the cementitious copolymer composition are applied to the damaged road surface.
  • Figure 1 is a graph plotting the results of the tensile strength and elongation testing:
  • Figure 2 is a graph plotting the results of the elongation testing of dispersions F1 to F5.
  • Figure 3 is a graph plotting the results of the tensile strength testing of dispersions F1 to F5
  • Figure 4 is a graph plotting the results of the deformation resistance by wheel tracking testing
  • the applicants have discovered a new cementitious copolymer composition which, when applied to an appropriate substrate surface will be highly flexible, water resistant and non-rigid, whilst have a high tensile strength, load bearing and impact resistance.
  • the composition of the present invention also remains highly water resistant. This prevents moisture water permeating through to the road substrate. This prevents the previously described breakdown of asphalt roads, a common cause of road failures.
  • Vinyl acetate + ethylene (VAE) dispersions are copolymers produced through dispersion polymerization of hard polar monomer vinyl acetate and soft hydrophobic monomer ethylene.
  • An optimal plasticizing monomer for vinyl acetate/ethylene functions as an internal plasticizer, which gives internal plasticity to VAE polymers, prevents plasticizer migration, and ensures lasting flexibility for VAE polymers.
  • VAE copolymers are characterized by high rotation freedom, low spatial hindrance, high backbone flexibility, stable structure, a certain degree of water resistance and a desirable degree of resistance to acids and alkalis.
  • the molecular chains of these copolymers are capable of maintaining stable properties in dilute acid and alkali conditions, by adjusting the polymer structure's copolymer component ratio, i.e. the ratio of vinyl acetate, ethylene or special functional monomers, to develop high-performance dispersions.
  • the drying time of the final product is influenced by the specific volumes of the various components of the composition of the present invention.
  • the Applicant has discovered that by increasing the volume of the cementitious additive, the drying time of the final product is also increased. This increased cementitious volume also influence the load bearing capability of the final product, though the deformation resistance will be decreased.
  • pest control additive may be added to the composition of the present invention without impacting the advantageous physical properties of the final product.
  • the pest control additive will form a barrier to deter pests. This is particularly useful when the product of the present invention for commercial and/or construction purposes.
  • Active ingredients for the pest control additives may include Bifenthhn, Chlorpy fos, Imidacloprid, Fipronil or other pest control additives known in the art.
  • V 320 is a polyvinyl alcohol) stabilized vinyl acetate-ethylene copolymer dispersion with a glass transition temperature (Tg) of +14 °C.
  • EP 701 is a polymer dispersion based on vinyl acetate and ethylene. This grade is designed as a plaster/plastic bonding agent and can use without plasticizer or solvent an additives to difficult bonding substrates.
  • EP 705K is a PVOH -protected vinyl acetate-ethylene copolymer of which viscosity is moderate and formaldehyde free.
  • the backbone of the polymer itself gives the dried adhesive film both toughness and flexibility which persist even with water immersion and fluctuations in temperature.
  • VINNAPAS® 5044 is a copolymer powder of vinyl acetate and ethylene. It is dispersible in water and has very good saponification resistance. Because of its relatively high ethylene content, this resin is soft and flexible.
  • Extendospheres are SG hollow spheres. Elongation
  • Figure 2 shows the results of the elongation testing of dispersions F1 to F5. As can be seen from the results the inclusion of the Extendospheres dramatically reduced the deformation ability of the final product.
  • Figure 3 shows the results of the tensile strength testing of dispersions F1 to F5. Again, the inclusion of the Extendospheres reduced the tensile strength of the final product.
  • Samples of the composition of the present invention underwent cyclonic missile impact testing in accordance with AS/NZS Standards (TMC39). Three 100 mm x 100mm sample panels of an average thickness of 8.2 mm were prepared for the purposes of the test. Specimens were placed in an Avery Denison Compression
  • the samples comprised of 85 volume percent of copolymer mixture; 10 volume weight of cementitious additive; and 5 volume weight percent of water.
  • the copolymer mixture used was LN 5408 (sourced from Wacker Polymers) which comprises approximately 85% vinyl acetate and approximately 15% ethylene and the cementitious additive was Ordinary Portland Cement (sourced from Boral Chemicals).
  • Table 1 Compression Test Results at 400 KN
  • Table 2 Compression Test Results at 600 KN
  • Samples of the composition of the present invention underwent deformation resistance by wheel tracking testing in accordance with Austroads Test Method AG- PT/T231 .
  • the samples comprised of 85 volume percent of copolymer mixure; 10 volume weight of cementitious additive; and 5 volume weight percent of water.
  • the copolymer mixture used was LN 5408 (sourced from Wacker Polymers) which comprises approximately 85% vinyl acetate and approximately 15% ethylene and the cementitious additive was Ordinary Portland Cement (sourced from Boral Chemcials).
  • Two 300 mm x 300mm sample panels of an average thickness of 50 mm were prepared for the purposes of the test. Specimens were mounted to the testing apparatus and wheel tracking on the sample was undertaken for a minimum of 10,000 load passes.
  • Figure 4 shows a plot of the results of the wheel tracking testing, showing relatively low rut depth for all samples after 20000 passes.
  • the composition of the present invention can be applied directly to surface areas by a ground spray application method. For high traffic areas, the coating is built up over multiple layers to obtain a final coating of approximately 12mm. a layer of gravel may also be provided between layer of the composition of the present invention in order to increase strength and to build up the thickness of the surface faster.
  • Road base coatings are constructed in such a way that usage can be obtained for weight distribution of between 40 to 150 tonne depending on specifications. It is suitable also for storage & lay down areas in isolated areas where access is limited and ground undulations are un-removable.
  • composition of the present invention when applied to large surface areas, the composition may be applied by way of a spray tanker.
  • the composition of the present invention may be applied to a pre-existing car park surface.
  • the composition may be sprayed over the car park bitumen or concrete surfaces to fully waterproof the substrate, and is rated to with stand high traffic weight volumes from 40 to 150 tonne, has also shown to have an exceptional wear factor on heavy traffic passes that exceeds existing road coatings.
  • the composition of the present invention When applied to the surface, the composition of the present invention repairs cracks, bonds the existing surface, and has a high wear factor. Once applied, the coating is UV stable, chemical resistant and waterproof, preventing moisture penetration entering the existing substrate.
  • composition of the present invention may also be utilised in commercial and construction applications where water damage is of concern. It is envisaged that the composition of the present invention may be used under slabs on commercial sites thus giving a seamless liner that can withstand moisture, or as a barrier on walls that require backfill. The addition of a pest control additive will provide additional resistance to insects.
  • the composition of the present invention may also be applied in protective situation in which it is utilised as a barrier to prevent the ingression of water. Under certain conditions, once applied, the composition can withstand over 5 Bar of pressure, thus giving total water stoppage and entrapment.
  • composition of the present invention may also be used to line shipping containers in order to increase their strength and to waterproof the container.
  • the composition of the present invention may also be applied to areas where corrosion has weakened the structure of the container. Sealing and prevention or retarding of rust development is then achieved both internally and externally as salt water will not penetrate or damage product coating once full cure has occurred. This also prevents salt water damage to the product being carried by the container.

Abstract

A cementitious copolymer composition comprising: 70 to 95 volume percent of a copolymer mixture; to 20 volume percent of a cementitious additive; and 0 to 10 volume percent of an aqueous solution.

Description

Cementitious Copolymer Composition
TECHNICAL FIELD
[0001 ] The present invention is directed towards a cementitious copolymer composition and a method for it use in the construction or repair of roads.
BACKGROUND ART
[0002] The following discussion of the background art is intended to facilitate an understanding of the present invention only. The discussion is not an acknowledgement or admission that any of the material referred to is or was part of the common general knowledge as at the priority date of the application.
[0003] Typically, road compositions are prepared from aggregate compositions of asphalt (bitumen) and rock, wherein the asphalt is utilised as a binder in order to create a hardened product which is laid over a rock or cement foundation. Asphalt pavement material is commonly composed of 5% asphalt cement and 95% aggregates (stone, sand, and gravel). Due to its highly viscous nature, asphalt cement must be heated so it can be mixed with the aggregates and spread across the intended surface.
[0004] For driver safety, the asphalt compositions must meet certain performance criteria or specifications in order to be considered useful for road paving. To ensure acceptable performance there are minimum standards set up by government
organisations which a composition must adhere to in order to be allowed to be used as road pavement. These minimum specifications relate to properties such as viscosity, toughness, tenacity and ductility.
[0005] If these specifications are not met, damage to the resulting road can occur, including permanent deformation, cracking and flexural fatigue. This damage greatly reduces the effective life of paved roads and ultimately driver safety.
[0006] Of the above issue, the cracking of the road surface is over the greatest concern. If proper drainage protocols are not in place, the cracks allow for moisture intrusion through the surface of the road and spread throughout the underlying aggregate material. The moisture will then sodden the material and over time, will break the asphalt / aggregate bond, damaging the integrity of the pavement material, causing the pavement to disintegrate. This then requires entire sections of the road to be dug up and new road be placed down.
[0007] Previously, it has been demonstrated that the properties of conventional asphalt compositions can be improved by the addition of other substances, such as polymers. A wide variety of polymers have been employed in asphalt compositions. For example, polymers derived from styrene and conjugated dienes are particularly useful, as these polymers have good solubility in asphalt compositions and the resulting modified compositions have improved physical properties.
[0008] U.S. Pat. No. 4, 145,322, discloses a process for preparing a bitumen-polymer composition consisting of mixing a bitumen, with a block copolymer, having an average molecular weight between 30,000 and 300,000. The colpolymer has the theoretical formula SxBy, in which S corresponds to styrene structure groups and B corresponds to conjugated diene structure groups, and x and y are integers. The resulting bitumen- polymer composition is used for road-coating, industrial coating, or other industrial applications. Whilst it remains that the majority of the physical properties of the resulting road composition are increased, they remain un-useful for the purposes of road compositions, mainly due to increased viscosity of the resulting product, where separation of the asphalt and polymer may occur.
[0009] Another concern of the use of asphalt compositions concerns the use of volatile solvents in such compositions. Specifically, environmental concerns restrict the use of volatile solvents in such compositions. Moreover, the use of large amounts of volatile solvents in bitumen compositions may lower the viscosity of the resulting composition so that it no longer meets viscosity specifications designated for road paving
applications. Additionally, the reduction of other emissions during asphalt applications becomes a target. For example, the reduction of the amount of sulfur compounds that are emitted during asphalt applications is of primary concern. These emissions are compounded by the fact that the asphalt is required to be heated substantially during the application process.
[0010] The present invention seeks to overcome, or at least ameliorate, one or more of the deficiencies of the prior art mentioned above, or to provide the consumer with a useful or commercial choice. [001 1 ] Those skilled in the art will appreciate that the invention described herein is susceptible to variations and modifications other than those specifically described. The invention includes all such variation and modifications. The invention also includes all of the steps, features, formulations and compounds referred to or indicated in the specification, individually or collectively and any and all combinations or any two or more of the steps or features.
[0012] Each document, reference, patent application or patent cited in this text is expressly incorporated herein in their entirety by reference, which means that it should be read and considered by the reader as part of this text. That the document, reference, patent application or patent cited in this text is not repeated in this text is merely for reasons of conciseness.
[0013] Throughout the specification, unless the context requires otherwise, the term "copolymer mixture" will be understood to be a polymerised composition of two or more monomeric species.
[0014] Throughout this specification, unless the context requires otherwise, the word "comprise" or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
SUMMARY OF INVENTION
[0015] In accordance with the present invention, there is provided a cementitious copolymer composition comprising:
70 to 95 volume percent of a copolymer mixture;
5 to 20 volume percent of a cementitious additive; and
0 to 10 volume percent of an aqueous solution.
[0016] As would be apparent from the current specification, the composition may include other components, thus the total volume percentage of the above components may not equal 100 percent. At times when the cementitious copolymer composition comprises only the above components, their total volume percentage will equal 100 percent.
[0017] In one form of the invention the cementitious additive comprises a Portland cement.
[0018] In one form of the present invention the cementitious additive comprises a blended cement
[0019] Preferably, the cementitious additive comprises:
10 to 90 percent by weight of Portland Cement clinker;
0 to 80 percent by weight of blast furnace slag;
0 to 60 percent by weight of fly ash;
0 to 10 percent by weight of silica flume;
3 to 8 percent by weight of gypsum; and
0 to 10 percent by weight limestone.
[0020] As would be apparent from the current specification, the cementitious additive may include other components, thus the total volume percentage of the above components may not equal 100 percent. At times when the cementitious additive comprises only the above components, their total volume percentage will equal 100 percent
[0021 ] In one form of the present invention the copolymer mixture may be provided as a resin
[0022] In one form of the present invention the copolymer mixture may be provided as a powdered solid.
[0023] In one form of the present invention, the copolymer consists one or more ethylenically unsaturated monomers. Preferably, the ethylenically unsaturated monomers are selected from the group consisting of vinyl esters, vinyl acetate methacrylates, methacrylic acid esters, vinylaromatics, olefins, 1 ,3-dienes and vinyl halides and optionally further monomers copolymerizable therewith.
[0024] Suitable monomers from the group of vinyl esters are, for example, those of carboxylic acids having 1 to 15 carbon atoms. Preferably, the monomer is selected from the group containing vinyl acetate, vinyl propionate, vinyl butyrate, vinyl 2- ethylhexanoate, vinyl laurate, 1 -methylvinyl acetate, vinyl pivalate and vinyl esters of branched monocarboxylic acids having 9 to 1 1 carbon atoms.
[0025] Suitable monomers from the group of methacrylic acid esters are, for example methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, n-butyl acrylate, n-butyl methacrylate, t-butyl methacrylate, t- butyl methacrylate, 2-ethylhexyl acrylate. Particularly preferred are methyl methacrylate, methyl acrylate, n-butyl methacrylate, t-butyl acrylate or 2-ethylhexyl acrylate.
[0026] Suitable monomers from the group of vinylaromatics are styrene, methyl styrene or vinyl toluenenyl.
[0027] A suitable monomer from the group of vinyl halides is vinyl chloride.
[0028] Suitable monomers from the group of olefins are ethylene, propylene, and the preferred dienes are 1 ,3-butadiene and isoprene.
[0029] In preferred form of the present the copolymer mixture is copolymer of one or more ninyl ester and ethylene. Still preferably the copolymer mixture is a vinyl acetate ethylene (VAE) resin.
[0030] Preferably, the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 99 to 75%, wherein the remainder of the content comprises ethylene.
[0031 ] Still preferably, the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 80 to 92%, wherein the remainder of the content comprises ethylene. In a highly preferred form of the present invention, the copolymer mixture comprises 86% vinyl acetate and 14% ethylene. [0032] In one form of the present invention, two or more vinyl acetate ethylene dispersions of varying monomer ratios are combined to provide the copolymer mixture.
[0033] In one form of the present invention the aqueous solution is water.
[0034] In one form of the present invention, the composition further comprises a pest control additive.
[0035] Preferably, the composition is adapted for application by a spray applicator, brush or roller. The viscosity of the cementitious copolymer composition may be controlled by the amount of aqueous solution in the composition.
[0036] In accordance with the present invention there is provided a method for coating a surface, the method comprising the steps of: preparing the surface; and applying one or more coats of the cementitious copolymer composition of the invention to the surface.
[0037] The surface may be bitumen, asphalt, concrete, compacted ground, graded ground, embankments, tailings dams, bunds for mines, or steel. Preferably, the surface is trafficable.
[0038] Preferably, the preparation of the surface comprises cleaning the surface. More preferably, the cleaning of the surface removes dirt, debris and/or any oils on the surface.
[0039] In one form of the present invention, the application of the cementitious copolymer composition is by way of a spray applicator, a roller or a brush.
[0040] Preferably, two coats of the cementitious copolymer composition are applied to the surface. Preferably still, three coats of the cementitious copolymer composition are applied to the surface. [0041 ] In one form of the present invention, a layer of gravel is applied between layers of the cementitious copolymer composition.
[0042] In one form of the present invention, the surface is a bitumen or concrete road.
[0043] Preferably, the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 1 and 15 mm. Preferably still the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 5 and 13 mm. Preferably still the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 8 and 12 mm.
[0044] In one form of the present invention, the method for coating of a surface may be used to coat steel structures in order to provide additional strength and water
resistance.
[0045] In one form of the present invention, the method for coating of a surface may be used to line the insides of shipping containers, in order to provide additional strength, provide rust resistance and waterproofing.
[0046] In accordance with the present invention, there is provided a method for the repair of damaged road surfaces, the method comprising the steps of: preparing the damaged road surface; and applying one or more coats of a cementitious copolymer composition of the invention to the damaged road surface.
[0047] Preferably, the preparation of the damaged road surface comprises cleaning the surface. Preferably the cleaning of the damaged surface removes dirt, debris and/or any oils on the surface.
[0048] In one form of the present invention, the application of the cementitious
copolymer composition is applied to the damaged road surface through a spray applicator, a roller or a brush. [0049] Preferably, two coats of the cementitious copolymer composition are applied to the damaged road surface. Preferably still, three coats of the cementitious copolymer composition are applied to the damaged road surface.
BRIEF DESCRIPTION OF THE DRAWINGS
[0050] Further features of the present invention are more fully described in the following description of several non-limiting embodiments thereof. This description is included solely for the purposes of exemplifying the present invention. It should not be understood as a restriction on the broad summary, disclosure or description of the invention as set out above. The description will be made with reference to the accompanying drawings in which:
Figure 1 is a graph plotting the results of the tensile strength and elongation testing:
Figure 2 is a graph plotting the results of the elongation testing of dispersions F1 to F5.
Figure 3 is a graph plotting the results of the tensile strength testing of dispersions F1 to F5
Figure 4 is a graph plotting the results of the deformation resistance by wheel tracking testing
DESCRIPTION OF EMBODIMENTS
Physical Characteristics of Components
[0051 ] In order for a composition to be utilised for the construction of roads its physical properties must adhere to a set of standard prerequisites.
[0052] The applicants have discovered a new cementitious copolymer composition which, when applied to an appropriate substrate surface will be highly flexible, water resistant and non-rigid, whilst have a high tensile strength, load bearing and impact resistance. [0053] Advantageously, due to its composition, the composition of the present invention also remains highly water resistant. This prevents moisture water permeating through to the road substrate. This prevents the previously described breakdown of asphalt roads, a common cause of road failures.
Co-polymers
[0054] Vinyl acetate + ethylene (VAE) dispersions are copolymers produced through dispersion polymerization of hard polar monomer vinyl acetate and soft hydrophobic monomer ethylene. An optimal plasticizing monomer for vinyl acetate/ethylene functions as an internal plasticizer, which gives internal plasticity to VAE polymers, prevents plasticizer migration, and ensures lasting flexibility for VAE polymers. VAE copolymers are characterized by high rotation freedom, low spatial hindrance, high backbone flexibility, stable structure, a certain degree of water resistance and a desirable degree of resistance to acids and alkalis. The molecular chains of these copolymers are capable of maintaining stable properties in dilute acid and alkali conditions, by adjusting the polymer structure's copolymer component ratio, i.e. the ratio of vinyl acetate, ethylene or special functional monomers, to develop high-performance dispersions.
Drying Time
[0055] The drying time of the final product is influenced by the specific volumes of the various components of the composition of the present invention. Advantageously, the Applicant has discovered that by increasing the volume of the cementitious additive, the drying time of the final product is also increased. This increased cementitious volume also influence the load bearing capability of the final product, though the deformation resistance will be decreased.
Pest Control Additive
[0056] The Applicant has also discovered that pest control additive may be added to the composition of the present invention without impacting the advantageous physical properties of the final product. The pest control additive will form a barrier to deter pests. This is particularly useful when the product of the present invention for commercial and/or construction purposes. Active ingredients for the pest control additives may include Bifenthhn, Chlorpy fos, Imidacloprid, Fipronil or other pest control additives known in the art.
Examples
[0057] Aspects of the present invention will now be illustrated with reference to a series of experimental examples. The description of the examples should not be understood to be limiting the generality of the preceding description of the invention. For the purposes of comparison, the experimental examples include reference to compositions outside the scope of the present invention. The inclusion of such compositions does not derogate from the preceding discussion
[0058] The following formations of the dispersion in various polymers where evaluated to determine rheology and elongation.
Figure imgf000011_0001
[0059] Wherein,
V 320 is a polyvinyl alcohol) stabilized vinyl acetate-ethylene copolymer dispersion with a glass transition temperature (Tg) of +14 °C.
EP 701 is a polymer dispersion based on vinyl acetate and ethylene. This grade is designed as a plaster/plastic bonding agent and can use without plasticizer or solvent an additives to difficult bonding substrates.
EP 705K is a PVOH -protected vinyl acetate-ethylene copolymer of which viscosity is moderate and formaldehyde free. The backbone of the polymer itself gives the dried adhesive film both toughness and flexibility which persist even with water immersion and fluctuations in temperature. Rheology
Figure imgf000012_0001
Tensile strength and elongation test results
The results of the tensile strength and elongation testing are shown in Figure 1 . As can be seen from Figure 1 , Formula 1 has the highest tensile strength, though the elongation testing shows a lower deformation resistance.
Elogation Testing
[0060] The following formations of the dispersion in various polymers where evaluated to compare elongation:
Figure imgf000012_0002
[0061 ] Wherein,
VINNAPAS® 5044 is a copolymer powder of vinyl acetate and ethylene. It is dispersible in water and has very good saponification resistance. Because of its relatively high ethylene content, this resin is soft and flexible.
Extendospheres are SG hollow spheres. Elongation
Figure 2 shows the results of the elongation testing of dispersions F1 to F5. As can be seen from the results the inclusion of the Extendospheres dramatically reduced the deformation ability of the final product.
Tensile Strength
Figure 3 shows the results of the tensile strength testing of dispersions F1 to F5. Again, the inclusion of the Extendospheres reduced the tensile strength of the final product.
Product Compression Testing
[0062] Samples of the composition of the present invention underwent cyclonic missile impact testing in accordance with AS/NZS Standards (TMC39). Three 100 mm x 100mm sample panels of an average thickness of 8.2 mm were prepared for the purposes of the test. Specimens were placed in an Avery Denison Compression
Machine and compressed at a speed of 1 m/min, a 5 kg steel planner 100mm x 51 mm section was placed over mounted specimen. The samples comprised of 85 volume percent of copolymer mixture; 10 volume weight of cementitious additive; and 5 volume weight percent of water. The copolymer mixture used was LN 5408 (sourced from Wacker Polymers) which comprises approximately 85% vinyl acetate and approximately 15% ethylene and the cementitious additive was Ordinary Portland Cement (sourced from Boral Chemicals).
[0063] The results of the compression testing indicate that the specimen was not compromised after being compressed at 400, 600 and 1500 KN for a 2 min load time. There was no evidence that the integral strength of the specimen itself being
compromised and the specimen returned to its normal thickness after 2 days. The results of each of the compression tests are shown in Tables 1 to 3.
Table 1 : Compression Test Results at 400 KN
Figure imgf000013_0001
Table 2: Compression Test Results at 600 KN
Figure imgf000014_0001
Table 3: Compression Test Results at 1500 KN
Figure imgf000014_0002
Deformation Resistance
[0064] Samples of the composition of the present invention underwent deformation resistance by wheel tracking testing in accordance with Austroads Test Method AG- PT/T231 . The samples comprised of 85 volume percent of copolymer mixure; 10 volume weight of cementitious additive; and 5 volume weight percent of water. The copolymer mixture used was LN 5408 (sourced from Wacker Polymers) which comprises approximately 85% vinyl acetate and approximately 15% ethylene and the cementitious additive was Ordinary Portland Cement (sourced from Boral Chemcials). Two 300 mm x 300mm sample panels of an average thickness of 50 mm were prepared for the purposes of the test. Specimens were mounted to the testing apparatus and wheel tracking on the sample was undertaken for a minimum of 10,000 load passes.
Table 4: Results of Deformation Resistance Testing
Figure imgf000014_0003
[0065] Figure 4 shows a plot of the results of the wheel tracking testing, showing relatively low rut depth for all samples after 20000 passes.
[0066] The results of the deformation resistance by wheel tracking testing demonstrated a compliance with AS/NZS standards and a relatively low rut depth. Application of the composition
[0067] Application of the composition of the present invention will now be illustrated with reference to a series of possible application methods. The description of the examples should not be understood to be limiting the generality of the preceding description of the invention.
Road Coatings
[0068] The composition of the present invention can be applied directly to surface areas by a ground spray application method. For high traffic areas, the coating is built up over multiple layers to obtain a final coating of approximately 12mm. a layer of gravel may also be provided between layer of the composition of the present invention in order to increase strength and to build up the thickness of the surface faster.
[0069] Road base coatings are constructed in such a way that usage can be obtained for weight distribution of between 40 to 150 tonne depending on specifications. It is suitable also for storage & lay down areas in isolated areas where access is limited and ground undulations are un-removable.
It is further envisaged that when the composition of the present invention is applied to large surface areas, the composition may be applied by way of a spray tanker.
Car Parks
[0070] The composition of the present invention may be applied to a pre-existing car park surface. The composition may be sprayed over the car park bitumen or concrete surfaces to fully waterproof the substrate, and is rated to with stand high traffic weight volumes from 40 to 150 tonne, has also shown to have an exceptional wear factor on heavy traffic passes that exceeds existing road coatings.
[0071 ] When applied to the surface, the composition of the present invention repairs cracks, bonds the existing surface, and has a high wear factor. Once applied, the coating is UV stable, chemical resistant and waterproof, preventing moisture penetration entering the existing substrate. Commercial/Construction
[0072] The composition of the present invention may also be utilised in commercial and construction applications where water damage is of concern. It is envisaged that the composition of the present invention may be used under slabs on commercial sites thus giving a seamless liner that can withstand moisture, or as a barrier on walls that require backfill. The addition of a pest control additive will provide additional resistance to insects. The composition of the present invention may also be applied in protective situation in which it is utilised as a barrier to prevent the ingression of water. Under certain conditions, once applied, the composition can withstand over 5 Bar of pressure, thus giving total water stoppage and entrapment.
Container lining
The composition of the present invention may also be used to line shipping containers in order to increase their strength and to waterproof the container. The composition of the present invention may also be applied to areas where corrosion has weakened the structure of the container. Sealing and prevention or retarding of rust development is then achieved both internally and externally as salt water will not penetrate or damage product coating once full cure has occurred. This also prevents salt water damage to the product being carried by the container.
[0073] Modifications and variations such as would be apparent to the skilled addressee are considered to fall within the scope of the present invention.

Claims

1 . A cementitious copolymer composition comprising:
70 to 95 volume percent of a copolymer mixture;
5 to 20 volume percent of a cementitious additive; and
0 to 10 volume percent of an aqueous solution.
2. A cementitious copolymer composition according to claim 1 , wherein the cementitious additive comprises a Portland cement.
3. A cementitious copolymer composition according to claim 1 , wherein the cementitious additive comprises a blended cement
4. A cementitious copolymer composition according to any one of the preceding claims, wherein the cementitious additive comprises:
10 to 90 percent by weight of Portland Cement clinker;
0 to 80 percent by weight of blast furnace slag;
0 to 60 percent by weight of fly ash; 0 to 10 percent by weight of silica flume; 3 to 8 percent by weight of gypsum; and 0 to 10 percent by weight limestone.
A cementitious copolymer composition according to any one of the preceding claims, wherein the copolymer mixture is provided as a resin.
A cementitious copolymer composition according to any one of claims 1 to 5, wherein the copolymer mixture is provided as a powdered solid.
7. A cementitious copolymer composition according to any one of the preceding claims, wherein the copolymer consists one or more ethylenically unsaturated monomers.
8. A cementitious copolymer composition according to claim 7, wherein the
ethylenically unsaturated monomers are selected from the group consisting of vinyl esters, vinyl acetate methacrylates, methacrylic acid esters, vinylaromatics, olefins, 1 ,3-dienes and vinyl halides and optionally further monomers
copolymerizable therewith.
9. A cementitious copolymer composition according to any one of the preceding claims, wherein the copolymer mixture is a vinyl acetate ethylene (VAE) resin.
10. A cementitious copolymer composition according to any one of the preceding claims, wherein the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 99 to 75%, and the remainder of the content comprises ethylene.
1 1 . A cementitious copolymer composition according to any one of the preceding claims, wherein the volume percentage of the vinyl acetate in the copolymer mixture is selected from the group comprising any one of 80% to 92% vinyl acetate and the remainder of the content comprises ethylene.
12. A cementitious copolymer composition according to any one of the preceding claims, wherein the copolymer mixture comprises 90% vinyl acetate and 10% ethylene.
13. A cementitious copolymer composition according to any one of claim 1 to 7, wherein two or more vinyl acetate ethylene dispersions of varying monomer ratios may also be combined to provide the copolymer mixture.
14. A cementitious copolymer composition according to any one of the preceding claims, wherein the aqueous solution is water.
15. A cementitious copolymer composition according to any one of the preceding claims, wherein the composition is adapted for application by a spray applicator, brush or roller.
16. A method for coating a surface, the method comprising the steps of: i. preparing the surface; and ii. applying one or more coats of the cementitious copolymer composition of the invention to the surface.
17. A method for coating a surface according to claim 16, wherein the surface may be bitumen, asphalt, concrete, compacted ground, graded ground,
embankments, tailings dams, bunds for mines, or steel.
18. A method according to claim 16 or claim 17 wherein, the surface is trafficable.
19. A method for coating a surface according to any one of claims 16 to 18, wherein the preparation of the surface comprises cleaning the surface.
20. A method for coating a surface according to claim 19, wherein the cleaning of the surface removes dirt, debris and/or any oils on the surface.
21 . A method for coating a surface according to any one of claims 16 to 20, wherein the application of the cementitious copolymer composition is by way of a spray applicator, a roller or a brush.
22. A method for coating a surface according to any one of claims 16 to 21 , wherein two coats of the cementitious copolymer composition are applied to the surface.
23. A method for coating a surface according to any one of claims 16 to 22, wherein three coats of the cementitious copolymer composition are applied to the surface.
24. A method for coating a surface according to any one of claims 16 to 23, wherein the surface is a bitumen or concrete road.
25. A method for coating a surface according to any one of claims 16 to 24, wherein the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 1 and 15 mm.
26. A method for coating a surface according to any one of claims 16 to 25, wherein the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 5 and 13 mm.
27. A method for coating a surface according to any one of claims 16 to 26, wherein the cementitious copolymer composition is applied in one or more coats such that the depth of the cementitious copolymer composition is between 8 and 16 mm.
28. A method for coating a surface according to any one of claims 16 to 27, wherein the method for coating of a surface may be used to coat steel structures in order to provide additional strength and water resistance.
29. A method for the repair of damaged road surfaces, the method comprising the steps of: i. preparing the damaged road surface; and ii. applying one or more coats of a cementitious copolymer composition of the invention to the damaged road surface.
30. A method for the repair of damaged road surfaces according to claim 29, wherein the preparation of the damaged road surface comprises cleaning the surface.
31 . A method for the repair of damaged road surfaces, according to claim 29 or 30, wherein the cleaning of the damaged surface removes dirt, debris and/or any oils on the surface.
32. A method for the repair of damaged road surfaces, according to any one of
claims 29 to 31 , wherein the application of the cementitious copolymer composition is applied to the damaged road surface through a spray applicator, a roller or a brush.
33. A method for the repair of damaged road surfaces, according to any one of
claims 29 to 32, wherein two coats of the cementitious copolymer composition are applied to the damaged road surface.
34. A method for the repair of damaged road surfaces, according to any one of
claims 29 to 33, wherein three coats of the cementitious copolymer composition are applied to the damaged road surface.
PCT/AU2013/000878 2012-08-08 2013-08-08 Cementitious copolymer composition WO2014022891A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101498872B1 (en) * 2014-07-24 2015-03-04 엄점동 Polymer Based Cement Waterproofing Agent With Improved Waterproof and Wear Resistance, and Preparing Method Thereof
KR101804454B1 (en) * 2016-03-24 2017-12-05 (주)제이엔티아이엔씨 Vinyl acetate-ethylene polymer modified concrete compostion and Method for pavement using the same
CN114477873A (en) * 2022-02-23 2022-05-13 深圳市宝金华混凝土有限公司 Recycled aggregate self-compacting concrete and preparation method thereof
CN114873953A (en) * 2022-07-08 2022-08-09 北京建筑大学 Water-based epoxy resin emulsified asphalt cold-mixing steel slag mixture and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614755A (en) * 1985-02-04 1986-09-30 Rodgers Jack L Protective coating composition comprising a blend of polyvinyl acetate, hydraulic cement, EVA, and limestone
US5185389A (en) * 1986-08-26 1993-02-09 Gemeng, Ltd. Latex modified mortar and concrete
US5244304A (en) * 1991-03-13 1993-09-14 American Stone-Mix, Inc. Cement based patching composition for asphalt pavement
WO1999005076A1 (en) * 1997-07-24 1999-02-04 M.J. Highway Technology Limited Road repair material comprising cement and a resin
US20080314295A1 (en) * 2005-03-22 2008-12-25 Nova Chemicals Inc. Lightweight concrete compositions
US20100041795A1 (en) * 2008-08-18 2010-02-18 Wilson Jr Jack H Pavement Life Extension Product and Method
US20120077906A1 (en) * 2010-09-23 2012-03-29 Wacker Chemie Ag Flexible Watertight Roof Coatings

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4614755A (en) * 1985-02-04 1986-09-30 Rodgers Jack L Protective coating composition comprising a blend of polyvinyl acetate, hydraulic cement, EVA, and limestone
US5185389A (en) * 1986-08-26 1993-02-09 Gemeng, Ltd. Latex modified mortar and concrete
US5244304A (en) * 1991-03-13 1993-09-14 American Stone-Mix, Inc. Cement based patching composition for asphalt pavement
WO1999005076A1 (en) * 1997-07-24 1999-02-04 M.J. Highway Technology Limited Road repair material comprising cement and a resin
US20080314295A1 (en) * 2005-03-22 2008-12-25 Nova Chemicals Inc. Lightweight concrete compositions
US20100041795A1 (en) * 2008-08-18 2010-02-18 Wilson Jr Jack H Pavement Life Extension Product and Method
US20120077906A1 (en) * 2010-09-23 2012-03-29 Wacker Chemie Ag Flexible Watertight Roof Coatings

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101498872B1 (en) * 2014-07-24 2015-03-04 엄점동 Polymer Based Cement Waterproofing Agent With Improved Waterproof and Wear Resistance, and Preparing Method Thereof
KR101804454B1 (en) * 2016-03-24 2017-12-05 (주)제이엔티아이엔씨 Vinyl acetate-ethylene polymer modified concrete compostion and Method for pavement using the same
CN114477873A (en) * 2022-02-23 2022-05-13 深圳市宝金华混凝土有限公司 Recycled aggregate self-compacting concrete and preparation method thereof
CN114873953A (en) * 2022-07-08 2022-08-09 北京建筑大学 Water-based epoxy resin emulsified asphalt cold-mixing steel slag mixture and preparation method thereof
CN114873953B (en) * 2022-07-08 2022-09-30 北京建筑大学 Water-based epoxy resin emulsified asphalt cold-mixing steel slag mixture and preparation method thereof

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