WO2010054989A2 - Revêtement antidérapant - Google Patents

Revêtement antidérapant Download PDF

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Publication number
WO2010054989A2
WO2010054989A2 PCT/EP2009/064754 EP2009064754W WO2010054989A2 WO 2010054989 A2 WO2010054989 A2 WO 2010054989A2 EP 2009064754 W EP2009064754 W EP 2009064754W WO 2010054989 A2 WO2010054989 A2 WO 2010054989A2
Authority
WO
WIPO (PCT)
Prior art keywords
component
composition
methoxypropanol
mpa
slip
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2009/064754
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German (de)
English (en)
Other versions
WO2010054989A3 (fr
Inventor
Friedrich Wagner
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Individual
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Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of WO2010054989A2 publication Critical patent/WO2010054989A2/fr
Publication of WO2010054989A3 publication Critical patent/WO2010054989A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50Amines
    • C08G59/5006Amines aliphatic
    • C08G59/502Polyalkylene polyamines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins

Definitions

  • the invention relates to an anti-slip coating and the processing of synthetic silica in nano-particle form as an additive in a composition or mixture, for use as a slip-resistant coating or floor covering with anti-slip properties.
  • skid resistance, slip resistance or slip resistance properties of floor coverings are summarized with and without reference to slip-promoting substances.
  • there are regulations and requirements for the slip resistance of floor coverings especially in industrial workspaces, but also in hospitals, shopping centers, kitchens, toilets, swimming pools or generally wet areas.
  • test pad is placed on a test rig and with a specific
  • the angle at which the examiner slips or feels insecure is determined and transferred to the following slip resistance classes:
  • R9 means: low coefficient of friction; Inclination angle> 3 ° - 10 °
  • RIO means: normal friction coefficient
  • Rl 1 means: increased coefficient of friction
  • R12 means: high static friction value; Inclination angle> 27 ° - 35 °
  • Rl 3 means: very high friction coefficient; Inclination angle> 35 °
  • builders and architects are increasingly paying attention to the required slip resistance classes when selecting floor coverings. More problematic is the retrofitting of old systems in which not the flooring material can be replaced, but by a new coating of the floor covering the required Slip safety class must be adjusted.
  • compositions and mixtures of paints and transparent binders are known which are offered as slip-resistant and non-slip floor coverings.
  • the known coatings In applications with non-exceptional stress in the home, business and public sector, and in particular if there is sufficient time to dry the coating, the known coatings also show more or less good levels of slip resistance and slip resistance.
  • VOCs volatile organic compounds
  • Such coatings have slow curing properties of up to 12 hours at 20 ° C. for drying and 24 hours for accessibility. For full cure under standard atmospheric conditions, 5 to 7 days are required for such coatings.
  • the addition of accelerators can reduce the drying time by about 50% and make coatings passable in 4 to 6 hours.
  • a major disadvantage of this acceleration is the strong odor, which is particularly dangerous indoors, so that the use of these coatings is often rejected by the customer.
  • Epoxy-based compositions have in normal case short pot life of up to 30 minutes and at standard temperature a drying time of up to 12 hours. Accelerators can significantly shorten the drying time, but also reduce the pot life and lead to significant yellowing, with more or less strong yellowing. The odor development is weaker compared to acrylic-based compounds and the abrasion values are significantly better. A serious disadvantage for the processing are the short pot lives. In addition, due to yellowing, epoxy-based compositions are often rejected by the customer.
  • the present invention therefore teaches a novel composition and its method of preparation and use, which is characterized in that it is an epoxy-based composition that is close to or completely free of VOCs.
  • the "A” component an intermediate molecular weight epoxy resin solution which can be diluted indefinitely with water, was used, for example, marketed under the name CHS-EPOXY 200 V 55 (Spolchemie, Czech Republic)
  • CHS-EPOXY 200 V 55 Spolchemie, Czech Republic
  • hydrophilic amorphous fumed silica in nanoparticulate form eg aerosils of types 300 and 200
  • the starting composition thus obtained hardens quickly and well, and is suitable for the creation of anti-slip, structured coatings. Since this composition is nearly smooth, glossy and forms only a slightly rough surface, this coating is suitable for smooth non-commercial surfaces, e.g. Bathtubs, but not for floor coverings that have to comply with the slip resistance classes RlO-Rl 3.
  • a decisive disadvantage is that usually at most about 10-14% of synthetic silica in nanoparticle form can be incorporated into the known coating mixture.
  • the term "silica in nanoparticulate form" are according to the
  • Ancillary application and the present invention fine fumed silica particles in size ranges from 2 to 70 nm, preferably 2-10 nm, 5-25 nm, 12-30 nm, 20-35 nm, 30- 45 nm and / or 50-60 nm to understand ,
  • the synthetic silicic acid originally produced by DEGUSSA in the flame hydrolysis of chlorosilanes, as well as the further development to pyrogenic, X-ray amorphous, synthetic silica - there are hydrophilic and hydrophobic products - are hereinafter referred to uniformly as synthetic silica or with the product name Aerosil.
  • the essential constituents of the novel composition are consequently the components "A” and "B” and an organic solvent, namely methoxypropyl acetate (MPA) and methoxypropanol in variable mixing ratios or only methoxypropanol.
  • MPA methoxypropyl acetate
  • methoxypropanol in variable mixing ratios or only methoxypropanol.
  • the preferred mixing ratio for optimum cure of the new composition is: Component A “: Component” B "equal to 100:26.
  • component A the ratio between component “A” and the additives shifts due to the different additives (eg synthetic silica, methoxypropanol etc.)
  • This relation factor always determines the amount of component "B” to be added.
  • the addition of component “B” will always be described with reference to component “A” for the sake of simplicity, so that if the relation factor of component "A” due to additions is for example 0.77, this value is included in the calculation and set equal to 100 according to the above-mentioned mixing ratio (100: 26).
  • the preferred mixing ratio of component "A" and the added organic solvent, preferably methoxypropanol or a mixture of methoxypropyl acetate and methoxypropanol corresponds to 1: 0.15-1.6, preferably 1: 0.15, 1: 0.5, 1: 0.75, 1: 1, 1: 1.2, or 1: 1.4.
  • the preferred mixing ratio of the mixture of methoxypropyl acetate and methoxypropanol is infinitely adjustable from 0: 1 to 1: 1.
  • the mixtures of methoxypropyl acetate and methoxypropanol can be made versatile depending on the nature of the use and need, since the inventive composition can be changed in their properties by the variable addition of MPA and methoxypropanol or only methoxypropanol.
  • the structure of the non-slip coatings may be low and almost imperceptible
  • MPA is classified as a structuring agent. It is believed, without being bound to this theory, that MPA is indeed capable of reducing the strong thickening effect of synthetic silica, the thixotropy, thereby forming compositions with strong but difficult to clean structures.
  • Methoxypropanol is also reduced in addition to the thixotropy of synthetic silica, moreover, it is believed that methoxypropanol acts as a thinner and so structures are formed, which are less strong and sharp-edged, but slightly rounded and therefore better to clean.
  • the composition of the invention forms in each case a hard-tough, transparent and partially glossy coating with exceptionally good slip-resistant properties; Slip-resistance classes of Rl 1-R13 can be achieved.
  • the inventive composition consists of 100 g of component "A” with 5-25 g of MPA, 5-10 g of methoxypropanol and 10-15 g of synthetic silica and further constituents and 30% of component "B” based on component "A.” This achieves an approximately slip-resistance class RIO.
  • the inventive composition consists of 100g component "A” with 5-15g MPA, 10-25g methoxypropanol and 15-25g synthetic Silica and other ingredients and 30% component "B” based on component "A”. This achieves about slip resistance class Rl 1.
  • the inventive composition consists of 100 g of component "A” with 5-15 g of MPA, 10-55 g of methoxypropanol and 15-25 g of synthetic silicic acid and further constituents and 20% of component "B” based on component "A" Slip safety class Rl 2.
  • the inventive composition consists of 100g component "A” with 5-10g MPA, 55-120g methoxypropanol and 20-35g synthetic silica, 40-8Og corundum and other ingredients and 22% component “B” based on component "A "- This reaches slip resistance class Rl 2-13.
  • the inventive composition consists of 100 g of component "A” with 25-140 g of methoxypropanol and 15-25 g of synthetic silica, 40-80 g of corundum and further constituents and 25% of component "B” based on component "A.”
  • This achieves anti-slip class It is particularly surprising in these compositions that, by adding an organic solvent, preferably methoxypropyl acetate (MPA) and / or methoxypropanol and other organic solvents having comparable properties, to the aqueous dispersion, an increase in the stirrable total amount of synthetic silica ( 20% and more) or other additives (up to 85%) is made possible and, notably, an improvement in the shelf life of the composition is nevertheless achievable.
  • MPA methoxypropyl acetate
  • an aliphatic epoxy-amines as a curing agent based on the component "A ", the MPA and / or the methoxypropanol, as well as other similarly acting solvents, is absorbed by the aqueous hardener and processed with the other proportions to form an elastic, homogeneous mixture in a very thorough mixture.
  • This mixture can then be applied with spatulas, rollers or other methods such as spraying, more or less strong on the surfaces to be coated, and optionally with the appropriate rollers or rackets / spatulas be reworked.
  • the coating cures to strongly structured slip-resistant or non-slip coverings.
  • a catalyst eg Telalit 0430
  • the curing time can be shortened.
  • catalyst eg Telalit 0430
  • the curing time can be shortened.
  • 0.5 and 2% catalyst based on the component "A” preferably 0.5%, 0.75%, 0.9%, 1.0%, 1.3%, 1.6% or 1.9 % added.
  • the coating mixtures of the aqueous epoxy resin solutions are named in the following EPSPOL and are classified according to an embodiment in different requirement classes (all classes are also upwards, divisible).
  • EPSPOL "light” with 5-8% addition of synthetic silicic acid e.g., Aerosil R 805 EPSPOL "medium” with 8.5-10% addition of synthetic silicic acid, e.g. Aerosil R 805 EPSPOL “strong” with 10.5-14% addition of synthetic silicic acid, for example Aerosil R 805 EPSPOL "super” with 14.5-20% addition of synthetic silicic acid, e.g. Aerosil R 805 Aerosil R 805 is selected as an example of a hydrophobic, amorphous, fumed silica. Other types of hydrophobic, fumed, synthetic silicic acid could also be used.
  • the relation factor always determines the amount of component "B” to be added in relation to component "A".
  • the recommended minimum addition of “B” is about 20%, but it can also be 30% and 40%, or any part in between.With 20% “B” and minimum solvent, the mixture is somewhat viscous elastic and forms Structures that are stiffer and do not tend to flow.
  • Such a coating composition may be sprayed, besides the usual application by means of a spatula, brush or roller, also with high performance and high pressure sprayers (e.g., GRACO) and the respective spray heads, to obtain non-slip coatings directly and in very uniform, fine, non-flowing structures.
  • high performance and high pressure sprayers e.g., GRACO
  • GRACO high performance and high pressure sprayers
  • the composition can also be applied or sprayed several times in order to intensify the anti-slip inhibition and to achieve a high abrasion resistance. Coatings with more solvent and a higher proportion of component "B" give less rigid structures, but cure equally well Such structures are still very good anti-slip, they are better and more wavy if they are finer and wavy Hygienic to clean, which is a required target especially in wet areas, clinics and swimming pools.
  • the proportion of synthetic silica is about 8-20%. This is a standard measure and it is difficult due to the strong thixotropy, but it is possible by the inventive composition to get higher proportions up to 30% or more.
  • the composition of the invention stirs more elastic-tough or slightly softer. In any case, it is very good to apply to all surfaces - tiles, stone, metal, wood, concrete, elastomers, PVC, laminate, etc - and forms structural coatings with anti-slip properties up to absolutely non-slip properties.
  • One such example is the blend, which can be adjusted by the content of aliphatic epoxy-polyamine in a tonnage range of up to 40%, yielding very high abrasion end products.
  • the increased abrasion and scratch resistance is especially in compositions containing further additives, and preferably further additives which are harder than silicon, e.g. Corundum, has been observed.
  • the slip resistance no longer results solely from the structure, so the nano-unevenness of the coating, but is influenced by the other additives. For example, prevents the added corundum thereby by forming a permeated with synthetic silica protective layer premature abrasion of the lower-value nanoparticles of snthetic silicic acid.
  • Crystalline quartzite is available in various sizes. For non-slip coatings it is suitable from 3000 MA up to 16900 MA. For the inventive
  • Anti-slip coating the finest quartzites are best suited as they combine with aqueous epoxy to give very hard surfaces.
  • quartz is at seven, high grade corundum at nine, and green silicon carbide at 9.5.
  • Commercially available corundum or Green Silicon Carbide are available in sizes of usually 53-42 microns to 15-6 microns down. For the smaller sizes, the slip-resistant green silicone carbide coatings are no more than greyish.
  • thermoplastic polyurethane ball pigments (Decosoft) and other abrasion-resistant or elastic rubber particles can be stirred up to a maximum degree of filling of 70% to 85% easily in the inventive composition.
  • Component A (EPOXY 200V 55) 100.00g MPA (methoxypropyl acetate) 8.00g
  • Aerosil R 805 (hydrophobic) 8-10,00g is added in small quantities and stirred in by hand if necessary.
  • component “A” EPOXY 200 V 55
  • MPA and the fumed silica AEROSIL R 805
  • AEROSIL R 805 fumed silica
  • Component B (TELALIT 180) 26.00g per 100g component "A"
  • composition thus obtained may be dried by means of tools, e.g. Rollers, spatulas, doctor blades or spray nozzles are applied. It dries on and off in the structures created by the work, almost without any flow.
  • tools e.g. Rollers, spatulas, doctor blades or spray nozzles are applied. It dries on and off in the structures created by the work, almost without any flow.
  • Component A (EPOXY 200 V 55) 100.00g
  • Aerosil R 805 (hydrophobic) 20-25,0Og
  • Component B (TELALIT 180) 26.00g each
  • composition thus obtained can be applied by means of tools, for example rollers, spatulas or doctor blades. It dries in the structures created by the work, leaving them slightly flattened and not sharp-edged. Optionally, these structures can be post-processed after a short drying phase. Coatings with slip resistance class Rl 2-13 (result of AlIg. SchuchtsAnstallt in Vienna) can be produced in this way. The coating thus produced is very easy to clean and has the highest abrasion values due to the high proportion of corundum.
  • Component A (EPOXY 200 V 55) 100.00g
  • Component B (TELALIT 180) 26.00g each
  • composition thus obtained may be dried by means of tools, e.g. Rolls, spatulas or squeegees are applied. It dries in the structures created by the work, leaving them slightly flattened and not sharp-edged.
  • tools e.g. Rolls, spatulas or squeegees are applied. It dries in the structures created by the work, leaving them slightly flattened and not sharp-edged.
  • the coating produced in this way is ideally suited to the wet area / barefoot areas, develops a gentle shine, is very easy to clean and shows highest abrasion values due to the corundum content.
  • Component A (EPOXY 200 V 55) 100.00g
  • Aerosil R 805 hydrophobic 8 - 10,00g Subsequent addition: Component B (TELALIT 180) 30.00g per 100g Component "A"
  • Component A (EPOXY 200 V 55) 100.00g
  • Aerosil R 805 (hydrophobic) 20-25,0Og
  • Component B (TELALIT 180) 26.00g each
  • Coating thickness should therefore be less than 1 mm. It can thus be produced coatings with slip resistance class Rl 2- 13.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

L'invention concerne un revêtement antidérapant et le traitement d'acide silicique pyrogène synthétique sous forme particulaire, en tant qu'additif dans une composition ou un mélange à employer en tant que revêtement antidérapant ou revêtement de sol à propriétés antidérapantes. Selon l'invention, une dispersion époxy aqueuse est diluée au moyen de solvants organiques, puis l'acide silicique pyrogène hydrophobe sous forme particulaire et d'autres additifs sont employés pour former une masse de revêtement.
PCT/EP2009/064754 2008-11-17 2009-11-06 Revêtement antidérapant Ceased WO2010054989A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AT17782008A AT507642A1 (de) 2008-11-17 2008-11-17 Rutschhemmende höhenaufbauende strukturbeschichtung unter verwendung von synthetischer kieselsäure im nanobereich für diverse oberflächen
ATA1778/2008 2008-11-17

Publications (2)

Publication Number Publication Date
WO2010054989A2 true WO2010054989A2 (fr) 2010-05-20
WO2010054989A3 WO2010054989A3 (fr) 2010-07-08

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Application Number Title Priority Date Filing Date
PCT/EP2009/064754 Ceased WO2010054989A2 (fr) 2008-11-17 2009-11-06 Revêtement antidérapant

Country Status (2)

Country Link
AT (1) AT507642A1 (fr)
WO (1) WO2010054989A2 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102016112699A1 (de) 2016-07-11 2018-01-11 Logis AG Verfahren zur Herstellung einer einseitigen Klebefolie zur Ladungssicherung und einseitige Klebefolie zur Ladungssicherung
CN108300414A (zh) * 2018-02-09 2018-07-20 佛山市大幸新材料有限公司 一种防滑纳米材料及其制备方法
CN111253833A (zh) * 2020-03-11 2020-06-09 柏林(惠州)科技化工有限公司 一种水性环氧洁净地坪涂料及其制作方法
CN113174777A (zh) * 2021-03-31 2021-07-27 美盈森集团股份有限公司 一种双组分涂布型防滑涂料及制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0696697B2 (ja) * 1990-08-17 1994-11-30 積水化学工業株式会社 接着剤組成物
US20050170188A1 (en) * 2003-09-03 2005-08-04 General Electric Company Resin compositions and methods of use thereof
JP2007504334A (ja) * 2003-09-03 2007-03-01 ゼネラル・エレクトリック・カンパニイ 溶媒改質樹脂組成物及びその使用法
US7498197B2 (en) * 2006-09-13 2009-03-03 Delphi Technologies, Inc. Silica nanoparticles thermoset resin compositions
KR100831095B1 (ko) * 2008-02-04 2008-05-22 김영동 미끄럼방지 조성물 제조방법 및 이를 이용한 미끄럼방지바닥 시공방법

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102016112699A1 (de) 2016-07-11 2018-01-11 Logis AG Verfahren zur Herstellung einer einseitigen Klebefolie zur Ladungssicherung und einseitige Klebefolie zur Ladungssicherung
WO2018011238A1 (fr) 2016-07-11 2018-01-18 Lohmann Gmbh & Co. Kg Procédé de fabrication d'un film adhésif sur une seule face destiné à immobiliser un chargement et film adhésif ainsi obtenu servant à immobiliser un chargement
US11208577B2 (en) 2016-07-11 2021-12-28 Lohmann Gmbh & Co. Kg Method for producing a single-sided adhesive film for securing a load and single-sided adhesive film for securing a load
CN108300414A (zh) * 2018-02-09 2018-07-20 佛山市大幸新材料有限公司 一种防滑纳米材料及其制备方法
CN111253833A (zh) * 2020-03-11 2020-06-09 柏林(惠州)科技化工有限公司 一种水性环氧洁净地坪涂料及其制作方法
CN113174777A (zh) * 2021-03-31 2021-07-27 美盈森集团股份有限公司 一种双组分涂布型防滑涂料及制备方法

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Publication number Publication date
WO2010054989A3 (fr) 2010-07-08
AT507642A1 (de) 2010-06-15

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