AU2018225296A1 - Improved coatings for pelletized thermoplastic pavement marking compositions - Google Patents
Improved coatings for pelletized thermoplastic pavement marking compositions Download PDFInfo
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- AU2018225296A1 AU2018225296A1 AU2018225296A AU2018225296A AU2018225296A1 AU 2018225296 A1 AU2018225296 A1 AU 2018225296A1 AU 2018225296 A AU2018225296 A AU 2018225296A AU 2018225296 A AU2018225296 A AU 2018225296A AU 2018225296 A1 AU2018225296 A1 AU 2018225296A1
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- 238000000576 coating method Methods 0.000 title claims abstract description 70
- 239000000203 mixture Substances 0.000 title claims abstract description 40
- 229920001169 thermoplastic Polymers 0.000 title claims abstract description 39
- 239000004416 thermosoftening plastic Substances 0.000 title claims abstract description 39
- 239000011248 coating agent Substances 0.000 claims abstract description 58
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000000463 material Substances 0.000 claims abstract description 36
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 26
- 239000001993 wax Substances 0.000 claims abstract description 26
- 239000004698 Polyethylene Substances 0.000 claims abstract description 16
- -1 polyethylene Polymers 0.000 claims abstract description 16
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 13
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 13
- 239000011230 binding agent Substances 0.000 claims abstract description 12
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 10
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920000573 polyethylene Polymers 0.000 claims abstract description 10
- 239000010457 zeolite Substances 0.000 claims abstract description 10
- 239000000945 filler Substances 0.000 claims abstract description 7
- 125000005625 siliconate group Chemical group 0.000 claims abstract description 7
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 6
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 17
- 239000004811 fluoropolymer Substances 0.000 claims description 12
- 229920002313 fluoropolymer Polymers 0.000 claims description 12
- 239000004115 Sodium Silicate Substances 0.000 claims description 9
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 7
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 5
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001343 alkyl silanes Chemical class 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 2
- 229910000077 silane Inorganic materials 0.000 claims 2
- 239000008188 pellet Substances 0.000 abstract description 54
- 238000010438 heat treatment Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 6
- 238000002844 melting Methods 0.000 abstract description 5
- 230000008018 melting Effects 0.000 abstract description 5
- 150000004756 silanes Chemical class 0.000 abstract description 4
- 239000004615 ingredient Substances 0.000 abstract description 3
- 150000004760 silicates Chemical class 0.000 abstract description 2
- 239000000843 powder Substances 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 9
- 239000011521 glass Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000002245 particle Substances 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 239000012815 thermoplastic material Substances 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 239000011324 bead Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000012768 molten material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- GBPOWOIWSYUZMH-UHFFFAOYSA-N sodium;trihydroxy(methyl)silane Chemical compound [Na+].C[Si](O)(O)O GBPOWOIWSYUZMH-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- HSFQBFMEWSTNOW-UHFFFAOYSA-N sodium;carbanide Chemical group [CH3-].[Na+] HSFQBFMEWSTNOW-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/004—Reflecting paints; Signal paints
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
A coating for pelletized thermoplastic road marking material is provided in which at least one of waxes, silica compounds, and inorganic compounds is provided on the surface of the thermoplastic pellet. The pellet is formed by mixing a binder mixture with a filler mixture, heating the mixed ingredients while mixing into a homogenous molten mixture and then extruding the molten mixture. The extruded material is cooled, cut into individual pellets and then coated. The coating prevents clumping of the pellets and also imparts improved flowability and lower melting point properties. Preferred coatings include micronized polyethylene wax, silicates, silanes, silicones, siliconates, fluoropoymers, calcium carbonate and zeolite.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation-in-part of co-pending application Serial No.
14/339,023 filed on July 23, 2014, entitled “Thermoplastic Pavement Marking Composition And Method,” which is a continuation-in-part of application Serial No. 14/329,462 filed on July 11, 2014, entitled Pelletizing System For Thermoplastic Pavement Marking Material, which is a continuation-in-part of application Serial No. 14/270,068 filed on May 5, 2014, entitled Pelletizing System For Road Surface Marking Material, the full disclosures of which are incorporated by reference herein and priority of which is hereby claimed.
BACKGROUND OF THE INVENTION [0002] Road surface markings are used on paved roadways to provide guidance and information to drivers and pedestrians. Road surface markings can be formed using mechanical or non-mechanical devices. Mechanical road surface markers may be raised or recessed into the road surface, and can be either reflective or non-reflective. Examples of mechanical markers are Botts' dots and rumble strips. Non-mechanical markers may be formed by paint, thermoplastic, preformed polymer tape, epoxy and other methods.
[0003] Thermoplastic markers are some of the most common types of road marking based on their balance between cost and performance longevity. Thermoplastic binder systems are generally based on one of three core chemistries: hydrocarbons, rosin esters, and maleic modified rosin esters (MMRE). Thermoplastic coatings are generally homogeneous dry mixes of binder resins, plasticizers, glass beads (or other optics), pigments, and fillers. These types of markers demonstrate increased durability, lasting 3 to 6 years, and retro-reflectivity.
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PCT/US2018/017041 [0004] Thermoplastic pavement markings are used in a hot-melt application process for various types of traffic control indicia. They are normally comprised of alkyd or hydrocarbon based resin systems, although hybrid versions of the materials can be formulated to impart favorable properties of each individual system into one combined system. Typically, thermoplastic pavement marking materials are used on roadways in longitudinal lines as edge and center-lines either as a continuous line or a skipped/dashed line. They can also be used for transverse markings such as stop bars, chevrons, traffic taming markings, bike and pedestrian crossings, railroad crossings, or similar markings. Thermoplastic pavement markings are used on public and private highways, public and private properties, airports, and parking lots.
[0005] Thermoplastic pavement are non-reactive coatings systems that are 100% solids materials composed of binder, pigment, glass beads, and inert fillers. Each state, and some cities and counties, govern the type and application of thermoplastic application by specifying the chemical composition and final film properties in terms of field performance over the lifecycle of the marking. Although most governmental agencies have their own internal and independent pavement marking specifications, thermoplastic pavement marking specifications are normally based on some variation of AASHTO M-249, which is a federal specification that sets minimum and basic requirements of the materials to be used. The binder is made up of a combination of rosin or petroleum based resins, plasticizing oils, elastomers, and viscosity and flow modifiers. The pigment for white materials is predominately Type II rutile titanium dioxide. The pigment for yellow materials is an organic based yellow pigment which can be a combination of yellow and red or orange pigments designed to withstand high temperatures and provide excellent UV resistance and weatherability. Glass beads are incorporated into the material so that as the material degrades under UV, water, and traffic exposure the glass beads will become exposed
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PCT/US2018/017041 and serve as reflective elements for nighttime visibility while under illumination from vehicles' headlamps. An exemplary compositional range for each component is as follows: binder 1826%, pigment (TiO2 only) 10-12% for white, N/A for yellow, and beads 30-40%.
[0006] Conventional thermoplastic mix is supplied in powdered form, which makes it difficult to load into the road marking machine. The technicians have to strictly follow safety regulations and use special equipment when preparing the marking mix. United States Patent No. 5,972,421 discloses a method for producing pelletized pavement marking mixtures in which each pellet is a homogeneous mixture of the desired thermoplastic composition. More recently, co-pending application Serial No. 14/329,482 filed on July 11, 2014, discloses a system of producing pelletized thermoplastic pavement marking material, which eliminates or significantly minimizes hazards associated with dust produced by powdered mixes. This application is directed to an apparatus and method of producing the thermoplastic pavement marking material in a pelletized form.
[0007] Co-pending application Serial No. 14/339,023, filed on July 23, 2014, discloses a composition suitable for use as a road marking substance. This composition is formed by mixing a binder mixture with a filler mixture, heating the mixed ingredients while mixing into a homogenous molten mixture and then extruding the molten mixture. The extruded material is cooled, cut into individual pellets, coated with an anti-clumping coating and packaged for use in making a road marking substance in situ. The binder can be alkyd-based or hydrocarbon based. The binder includes rosin resins, wax and a plasticizer, and a hydrocarbon resin is added for the hydrocarbon-based binder. The filler contains titanium dioxide, a pigment (if necessary) and ground calcium carbonate. The pellet coating material can be a member selected from a group
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PCT/US2018/017041 containing kaolin clay, calcium carbonate, calcined clay, micronized waxes and other antidumping materials or a combination of materials.
SUMMARY OF THE INVENTION [0008] A coating for pelletized thermoplastic road marking material is provided in which at least one of waxes, silica compounds, and inorganic compounds is provided on the surface of the thermoplastic pellet. The pellet is formed by mixing a binder mixture with a filler mixture, heating the mixed ingredients while mixing into a homogenous molten mixture and then extruding the molten mixture. The extruded material is cooled, cut into individual pellets and then coated. The coating prevents clumping of the pellets and also imparts improved flowability and lower melting point properties. Preferred coatings include micronized polyethylene wax, silicates, silanes, silicones, siliconates, fluoropoymers, calcium carbonate and zeolite.
BRIEF DESCRIPTION OF THE DRAWINGS [0009] Figure lisa photograph showing the results of a deformation test performed on a standard thermoplastic material and a thermoplastic material made in accordance with the present invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS [0010] By creating pellets of the pavement marking material, a homogeneous dust-free product is produced that has substantially less dust than conventional dry-blend or powder mixes. The pavement marking composition produced using pelletized materials is homogenized during manufacturing, thereby producing compositionally identical particles. Having particles that are identical allows for increased process control and monitoring. Theoretically, one particle can be
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PCT/US2018/017041 tested for composition and physical properties due to the homogenous nature of the finished product. Smaller samples can be taken with greater certainty of testing accuracy.
[0011] In co-pending application Serial No. 14/339,023, a coating is applied to the extruded and dried pellets in a pellet coating barrel or vessel which is mounted below a coating container which houses a pellet coating material. A weight loss load cell can be operationally connected to the coating container in order to regulate delivery of the pellet-coating material to the pellet coating vessel.
[0012] The pellet coating process modifies the surface of the pellets so that they will remain free flowing after packaging and storage. The free flowing nature of the material is necessary for ease of use during application. In one embodiment, the pelletized material is deposited into a smooth walled, rotating barrel with an angled axis inclined toward the pellet source. As the material falls into the rotating barrel, the coating agent is metered from the coating container into the barrel at a flow rate controlled by the control unit in the form of the weight loss cell. As an alternative, the pellets can be coated by suspending the pellet coating as solution in the water used to cool and transport the material.
[0013] Applicants have found that the coated pellets show improved handling performance beyond their anti-clumping behavior. The coated pellets have a lower melting point than powder mixtures and also exhibit improved flowability properties.
[0014] Applicants have found that a new series of coatings that provides improved antidumping properties at elevated temperatures
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PCT/US2018/017041 [0015] Coatings for thermoplastic pellets can be prepared from organic compounds such as waxes, various silica based compounds like silanes, silicones, siliconates and fluoropolymers; or inorganic compounds such as calcium carbonate, silica, or zeolite. Waxes are a group of organic compounds containing long alky chains and not soluble in water. They are derived from animals, plants, petroleum, and synthetic sources. In a first preferred embodiment, the coating for the pellets is an aliphatic hydrocarbon such as micronized polyethylene wax (Polyspherse W2S). In a second preferred embodiment, the coating for the pellets is a silica compound selected from the group of functionalized silanes, such as amino or alkyl silanes; silicones, such as alkyl silicones; or siliconates, such as sodium methlysiliconate. In a third preferred embodiment, the coating for the pellets is a fluoropolymer, such as Capstones brand (DuPont), which can be either cationic or anionic. In a fourth preferred embodiment, the coating for the pellets is an inorganic compound such as silica, calcium carbonate, sodium silicate or a zeolite. Preferred silica compounds include nano silica solutions, silica emulsions, and sodium silicate. Small particle size zeolite powder is preferred. Examples of additional coating compounds that can be used are polyethylene wax (Polyspherse W2F), amino silane (DC Z-6011), silicone emulsion, siliconate (sodium methyl silconate DC-772), nano silica (Ludox AS-30), sodium silicate, and zeolite powder (PQ corporation CBV760).
[0016] In addition to preventing the pellets from clumping, it has been found that the presently preferred coatings improve the performance of the road marking. When melted with the rest of the pellet prior to application on the roadway, the coating will enhance the ability of the marking to resist deformation under the pressure of vehicular traffic. This allows the roadway marking to remain true and not spread out or otherwise smear. The preferred polyethylene wax coating will also lower the melt temperature of the pellet, reducing the energy
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PCT/US2018/017041 needs to melt the pellets and also allowing the marking application system to operate at a lower, safer temperature. The polyethylene wax coating also improves the flowability of the melted pellets, thereby allowing the road markings to be applied at a quicker rate.
Experiment 1.
[0017] Melting point comparison. The following data presented in Table 1 shows that the pelletized thermoplastic described in this invention has a lower melt temperature compared to conventional powder thermoplastics. In a metal can, 100 grams of each thermoplastic product was heated on a hot plate and the temperature was measured when the product melted and was easily stirred by a spatula.
TABLE 1
| Products | Melting point (° F) |
| Powder thermo (Ennis Flint) | 334 |
| Pelletized thermo PE wax coated | 268 |
| Pelletized thermo CaCO3 coated | 273 |
Experiment 2, [0018] Melt flow properties. One hundred grams of thermoplastic product was placed in a metal can and heated on a hot plate until it melted and became a viscous fluid. The can was then placed at a 45° angle and the contents were allowed to flow and captured in another container placed below. The weight of the material that flowed into the second can was determined and a flow rate was calculated for the thermoplastic product. Thermoplastic products having a higher flow rate were more easily able to flow out of the thermoplastic tank.
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PCT/US2018/017041
TABLE 2
| Products | Flow rate (%) |
| Powder thermo (Ennis Flint) | 45.2 |
| Pelletized thermo PE wax coated | 59.3 |
| Pelletized thermo CaCO3 coated | 54.1 |
Experiment 3, [0019] Anti-clumping properties. Most thermoplastic materials are stored in a closed, metal tank for a period of time before lane striping. Depending on the ambient temperature, the inside temperature of the tank will be significantly higher than the ambient temperature. Under such conditions, the thermoplastic material is susceptible to clumping and becomes difficult to transfer to the container on the truck. The following experiment was carried out to determine the effect of temperature. The pelletized thermoplastic product with polyethylene wax was washed with hexane/toluene followed by acetone to remove all surface coatings. The pelletized thermoplastic material with calcium carbonate was washed with 0.5N hydrochloric acid followed by water then air dried. Each thermoplastic pellet sample (50 grams) was placed in a glass beaker and placed in an oven at 150°F (65.6°C) and the product was observed for clumping. After heating for 45 minutes at 150°F, the samples without coating clumped heavily and formed a thick mass, but the pellets with coatings remained as pellets without sticking and were able to be poured out of the beaker. The same trend was also observed after heating for 2 hours at 150°F. The results of this experiment are presented in Table 3 below.
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PCT/US2018/017041
TABLE 3
| Products | Physical form after 45 min at 150°F |
| Pelletized thermo PE wax coated | Pellets easy flow |
| Pelletized thermo without PE wax coating | Clumped to thick mass |
| Pelletized thermo CaCO3 coated | Pellets easy flow |
| Pelletized thermo without CaCO3 coating | Clumped to thick mass |
Experiment 4, [0020] Additional anti-clumping coatings. A one liter metal container was placed in a rotating tumbler and 100 grams of uncoated thermoplastic pellets were added. A series of coating compositions set forth in Table 4 below were prepared (about 30% of active chemical in water) and 4g of these solutions were added to the pellets while rotating, and rotated further for 5 minutes. In the case of zeolite powder, 3 grams of water was first sprayed onto the pellets and 2 grams of the powder was added slowly white rotating. The coated thermoplastic pellets (50 grams) were placed an 80 mL glass beaker and heated in an oven at 140°F (60°C), 160°F (71.1 °C), and 180°F (82.2°C) for the specified time and the glass beaker was taken out and the contents were poured out and observed for any clumping. The results are summarized below in Table 4. All coating chemicals mentioned in Table 4 show better anti-clumping effect than PE wax up to 160° F.
TABLE 4
| Coating chemicals on pellets | After lh at 140° F | After 2h at 140° F | After 2h at 160° F | After 2h at 180° F |
| No chemical (uncoated) | Clumped | Clumped | Clumped | Clumped |
| PE wax | No clumping | Clumped | Clumped | Clumped |
| Silicone emulsion | No clumping | No clumping | No clumping | Clumped |
| Nano silica | No clumping | No clumping | No clumping | Clumped |
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PCT/US2018/017041
| Coating chemicals on pellets | After lh at 140° F | After 2h at 140° F | After 2h at 160° F | After 2h at 180° F |
| Capstone FS-63 | No clumping | No clumping | No clumping | Clumped |
| Sodium methyl siliconate | No clumping | No clumping | No clumping | Clumped |
| Amino silane | No clumping | No clumping | No clumping | Clumped |
| Sodium silicate | No clumping | No clumping | No clumping | No clumping |
| Zeolite powder | No clumping | No clumping | No clumping | No clumping |
Experiment 5, [0021] The PE Wax coating/PE Wax in the material formulation also imparts to the thermoplastic pellets the ability to resist deformation at low temperatures. This property is important for pelletized thermoplastic because if the pellets deform during storage, they will form a physical bridge that will prevent them from flowing readily during use.
[0022] In an aluminum can or similar container, 500 grams of thermoplastic material was melted in an oven at 400°F (204.4°C) for 4 hours. The can containing the molten material was removed from the oven and the contents were stirred for 5 seconds with a suitable long blade spatula. Approximately 50-200 grams of the molten material was poured onto a non-stick surface to form a thin, circular disc of molten material. The disc should be less than 1/2 inch thick having a diameter of 2- 3 inches. After the disc was cooled to room temperature, the disc was suspended over a 2 inch crevasse in an incubator oven at 115°F (46.1°C). After 48 hours, the samples were monitored for deformation.
[0023] The results of this experiment are shown in Figure 1. A standard thermoplastic pellet (labeled 9902 in Figure 1) showed notable deformation. In contrast, the wax coated / containing thermoplastic pellet showed no movement.
WO 2018/156348
PCT/US2018/017041 [0024] Although Experiment 5 was conducted using polyethylene wax, it is expected that the same resistance to thermal deformation would likewise occur if the coating were formed using any of the compositions set forth in Table 4.
[0025] In addition, the coatings listed above can be combined with one another and used in combination. For example, a coating can be formed using sodium silicate combined with amino silane or a silicone emulsion. Likewise, nano silica can be combined with amino silane or a silicone emulsion to form a coating. An additional coating can be formed by combining sodium methyl siliconate with nano silica or sodium silicate. Furthermore, a coating can be formed by combining amino silane or sodium silicate or nano silica with glass dust having an average size between 5 and 70 microns.
[0026] The pellets produced in accordance with the present invention have superior storage stability. The pellets or particles are in the same physical form that is placed on the highway as an exterior, UV and weather resistant coating. Therefore, the pellets can withstand exposure to moisture, heat, humidity for longer periods than the current products on the market. Conventional dry blend products are produced in a powder form that will absorb moisture and become a solid compressed block over a long storage time. Moisture content causes increased energy to vaporize the moisture and the increased energy and heat will also cause color and physical property degradation. When the material becomes compressed the melt time, energy consumed, and labor requirement is greatly increased. Block material can withstand moisture as well, but the boxes that it is packaged in can get wet and become a nuisance and efficiency killer for crews. Generally, thermoplastic is considered to have a one-year storage life when stored indoors, away from direct contact with water. The pellet materials produced according to this invention could see that longevity at least doubled.
WO 2018/156348
PCT/US2018/017041 [0027] It is envisioned that the pellets can be used in conventional melt vessels and application operations, as well as tankless application operations. In a tankless process, no material would be heated in melt vessels or kettles. The pellets or particles would be added manually, pneumatically, or by other automatic or semi-automatic conveyance to a system of pipes and extruders capable of heating the material on demand and without any preheating.
[0028] It will be apparent to those skilled in the art that numerous modifications and variations of the described examples and embodiments are possible in light of the above teachings of the disclosure. The disclosed examples and embodiments are presented for purposes of illustration only. Other alternate embodiments may include some or all of the features disclosed herein. Therefore, it is the intent to cover all such modifications and alternate embodiments as may come within the true scope of this invention, which is to be given the full breadth thereof. Additionally, the disclosure of a range of values is a disclosure of every numerical value within that range, including the end points.
WO 2018/156348
PCT/US2018/017041
Claims (18)
- We claim:1. A coating for pelletized thermoplastic road marking material comprising at least one of waxes, silica compounds, and inorganic compounds.
- 2. The coating of claim 1, wherein said coating is a micronized polyethylene wax.
- 3. The coating of claim 1, wherein said coating is one of a silicate, functionalized silane, silicone, and siliconate.
- 4. The coating of claim 3, wherein the coating is one of a group of amino or alkyl silanes, alkyl silicones and sodium methlysiliconate.
- 5. The coating of claim 1, wherein said coating is a fluoropolymer.
- 6. The coating of claim 5, wherein said fluoropolymer is a cationic fluoropolymer.
- 7. The coating of claim 5, wherein said fluoropolymer is a anionic fluoropolymer.
- 8. The coating of claim 1, wherein said coating is one of a calcium carbonate and a zeolite.
- 9. The coating of claim 1, wherein the silica compound is one of a nano silica solution, silica emulsion, and sodium silicate.
- 10. A composition for coating a pelletized road marking composition formed from a binder mixture comprising one or more member selected from the group consisting of rosin resins, waxes, and plasticizers, and a filler mixture comprising reflective elements, said coating comprising one of waxes, silica compounds, and inorganic compounds.
- 11. The composition of claim 10, wherein said coating is a micronized polyethylene wax.
- 12. The composition of claim 10, wherein said coating is one of a silicate, functionalized silane, silicone, and siliconate.WO 2018/156348PCT/US2018/017041
- 13. The composition of claim 12, wherein the coating is one of a group of amino or alkyl silanes, alkyl silicones and sodium methlysiliconate.
- 14. The composition of claim 10, wherein said coating is a fluoropolymer.
- 15. The composition of claim 14, wherein said fluoropolymer is a cationic fluoropolymer.
- 16. The composition of claim 14, wherein said fluoropolymer is a anionic fluoropolymer.
- 17. The composition of claim 10, wherein said coating is one of a calcium carbonate and a zeolite.
- 18. The composition of claim 10, wherein the silica compound is one of a nano silica solution, silica emulsion, and sodium silicate.WO 2018/156348PCT/US2018/0170411/1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/440,475 | 2017-02-23 | ||
| US15/440,475 US10308816B2 (en) | 2014-05-05 | 2017-02-23 | Coatings for pelletized thermoplastic pavement marking compositions |
| PCT/US2018/017041 WO2018156348A1 (en) | 2017-02-23 | 2018-02-06 | Improved coatings for pelletized thermoplastic pavement marking compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2018225296A1 true AU2018225296A1 (en) | 2019-09-19 |
Family
ID=63253979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2018225296A Abandoned AU2018225296A1 (en) | 2017-02-23 | 2018-02-06 | Improved coatings for pelletized thermoplastic pavement marking compositions |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP3585842A1 (en) |
| JP (1) | JP2020508386A (en) |
| AU (1) | AU2018225296A1 (en) |
| WO (1) | WO2018156348A1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11702804B2 (en) | 2018-09-25 | 2023-07-18 | Ennis-Flint, Inc. | Thermoplastic pavement marking composition |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3867178A (en) * | 1972-09-05 | 1975-02-18 | Potters Industries Inc | Method for coating discrete particles |
| CA1268016A (en) * | 1984-09-21 | 1990-04-24 | Robert Dejaiffe | Reflective particles and method of making the same |
| US5665793A (en) * | 1994-06-09 | 1997-09-09 | Anders; Irving | Phosphorescent highway paint composition |
| US5928716A (en) * | 1996-04-12 | 1999-07-27 | Stimsonite Corporation | Method for marking a roadway surface |
| US5972421A (en) | 1996-04-12 | 1999-10-26 | Stimsonite Corporation | Method for producing pelletized pavement marking mixtures |
| JP2000136248A (en) * | 1998-08-28 | 2000-05-16 | Toray Ind Inc | Thermoplastic elastomer pellet and production of molded product |
| JP2000160058A (en) * | 1998-09-24 | 2000-06-13 | Hitachi Chemical Industrial Material Co Ltd | Melting type marking material |
| US6482519B1 (en) * | 2000-12-29 | 2002-11-19 | Innovative Concepts Unlimited | Coated microparticles, plastic compositions and methods |
| JP2002293946A (en) * | 2001-01-26 | 2002-10-09 | Kanegafuchi Chem Ind Co Ltd | Method for preventing blocking of isobutylene-based block copolymer pellets |
| JP2005015597A (en) * | 2003-06-25 | 2005-01-20 | Nippon Zeon Co Ltd | Petroleum resin composition and hot melt type road marking paint composition |
| US7501019B2 (en) * | 2005-03-31 | 2009-03-10 | Chevron U.S.A., Inc. | Granular solid wax particles |
| JP2008063496A (en) * | 2006-09-08 | 2008-03-21 | Toda Kogyo Corp | Colorant for road marking material and paint composition for road marking material produced by using colorant for road marking material |
| JP5261958B2 (en) * | 2007-03-30 | 2013-08-14 | 住友化学株式会社 | Method for producing olefin polymer pellets |
| FI125654B (en) * | 2008-06-13 | 2015-12-31 | Finncabin Ltd Oy | Method and apparatus for mixing and feeding solids and binders |
| DE102013206116A1 (en) * | 2013-04-08 | 2014-10-09 | Evonik Industries Ag | New road markings to support the perception of the surroundings of vehicles |
| US9771492B2 (en) * | 2014-05-05 | 2017-09-26 | Daniel John Puffer | Thermoplastic pavement marking composition and method |
| JP2016188327A (en) * | 2015-03-30 | 2016-11-04 | 住友精化株式会社 | Self-adhesion preventive agent |
-
2018
- 2018-02-06 AU AU2018225296A patent/AU2018225296A1/en not_active Abandoned
- 2018-02-06 EP EP18706355.7A patent/EP3585842A1/en not_active Withdrawn
- 2018-02-06 JP JP2019546875A patent/JP2020508386A/en active Pending
- 2018-02-06 WO PCT/US2018/017041 patent/WO2018156348A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018156348A1 (en) | 2018-08-30 |
| JP2020508386A (en) | 2020-03-19 |
| EP3585842A1 (en) | 2020-01-01 |
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