Thermoplastic pavement marking composition
11702804 · 2023-07-18
Assignee
Inventors
- Govindasamy Paramasivam Rajendran (Garnet Valley, PA)
- Mark Terry (Madison, MS, US)
- Jeffrey Lee Stricker (Narberth, PA, US)
Cpc classification
C09D167/08
CHEMISTRY; METALLURGY
C09D167/08
CHEMISTRY; METALLURGY
B29B9/12
PERFORMING OPERATIONS; TRANSPORTING
B29B13/022
PERFORMING OPERATIONS; TRANSPORTING
B29B9/06
PERFORMING OPERATIONS; TRANSPORTING
E01F9/506
FIXED CONSTRUCTIONS
C08J2367/07
CHEMISTRY; METALLURGY
B29B7/726
PERFORMING OPERATIONS; TRANSPORTING
B29B2009/125
PERFORMING OPERATIONS; TRANSPORTING
C08J3/203
CHEMISTRY; METALLURGY
International classification
B29B9/12
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A pelletized road marking composition includes a binder mixture, a filler mixture and bentonite clay. The binder mixture includes at least one alkyd ester, at least one wax, at least one ethylene copolymer, and at least one plasticizer. The filler mixture includes at least one coloring additive, reflective elements, and at least one inert inorganic filler. The components of the road marking composition are mixed and melted and processed into pellets. The bentonite clay added to the composition prevents the pellets from clumping when stored at elevated temperatures.
Claims
1. A road marking composition comprising: a binder mixture comprising an alkyd ester, a wax, an ethylene copolymer, and a plasticizer; a filler mixture comprising a coloring additive, reflective elements, and an inorganic filler; and bentonite clay therein, said road marking composition formed into pellets.
2. The composition of claim 1, wherein said bentonite clay is an organic modified bentonite.
3. The composition of claim 1, wherein the amount of said bentonite clay in said composition ranges from 0.01 to 5.0 percent by weight.
4. The composition of claim 3, wherein the amount of said bentonite clay in said composition ranges from 0.1 to 2.0 percent by weight.
5. The composition of claim 1 further comprising a glass fill viscosity modifier.
6. The composition of claim 5, wherein the amount of said glass fill is in the range of 25 to 40 percent by weight.
7. A method for manufacturing the road marking composition of claim 1 comprising the steps of: heating a mixture of the binder mixture, the bentonite clay, and the filler mixture to form a molten composition; processing said molten composition into a plurality of pellets; and cooling and drying the plurality of pellets.
8. The method of claim 7, wherein said bentonite clay is an organic modified bentonite.
9. The method of claim 7, wherein the amount of said bentonite clay in said composition ranges from 0.01 to 5.0 percent by weight.
10. The method of claim 9, wherein the amount of said bentonite clay in said composition ranges from 0.1 to 2.0 percent by weight.
11. The method of claim 7 further comprising the step of adding a glass fill viscosity modifier before heating said thermoplastic composition.
12. The method of claim 11, wherein the amount of said glass fill is in the range of 25 to 40 percent by weight.
13. The composition of claim 1, wherein the ethylene copolymer comprises ethylene vinyl acetate.
14. The composition of claim 1, wherein the ethylene copolymer comprises of one or more of ethylene vinyl acetate copolymers, ethylene acrylate copolymers, ethylene methacrylate copolymers, ethylene acrylate glycidyl-acrylate copolymers.
15. The composition of claim 1, wherein the ethylene unit of the ethylene copolymer ranges from 50 to 95 percent by weight of the total ethylene copolymer.
16. The composition of claim 1, wherein the road marking composition formed into pellets does not include a calcium carbonate coating.
17. The composition of claim 1, wherein the composition comprises a clump strength of at least 82 psi.
18. The composition of claim 3, wherein the amount of said bentonite clay in said composition ranges from 0.5 to 1.0 percent by weight.
Description
DETAILED DESCRIPTION OF THE INVENTION
(1) While the present invention will be described with reference to preferred embodiments, it will be understood by those who are skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. It is therefore intended that the present invention not be limited to the particular embodiments disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments and legal equivalents thereof which are within the scope of the appended claims.
(2) The present invention is a pelletized thermoplastic road marking composition that is specially designed to minimize clumping of the pellets when exposed to hot storage conditions. The thermoplastic road marking composition is formed from a mixture of thermoplastic binders, inorganic fillers, and bentonite clay. The thermoplastic binder includes an alkyd resin, a plasticizer, ethylene copolymer (EVA), and polyethylene wax. The filler includes titanium dioxide, calcium carbonate, and retroreflective glass beads. It has been found that the bentonite clay added to the thermoplastic road marking composition minimizes the clumping of the pellets.
(3) Suitable alkyd resins include rosin resin, which is comprised of one or more components consisting of modified rosin resins and rosin esters. Modified rosin resins are comprised of one or more components consisting of rosin acids, maleic anhydride and fumaric acid. Rosin acid is derived from pine trees as gum rosin, wood rosin and tall oil rosin. Rosin esters are comprised of one or more derivatives obtained from the reaction of one or more rosin acids and one or more alcohol from the group of alcohols consisting of methanol, triethylene glycol, glycerol and penta-erythritol.
(4) Suitable plasticizers include vegetable oils and phthalates. Vegetable oils are the reaction products of the fatty acids with glycerol, commonly referred to as triglycerides; castor oil is a typical example. Phthalates are comprised of one or more components from a group of esters such as dimethyl phthalate, diethyl phthalate, dibutyl phthalate, dicyclohexyl phthalate, butyl(2-ethylhexyl) phthalate and similar such phthalate ester compounds.
(5) The waxes used in the thermoplastic composition include petroleum-derived waxes and synthetic waxes. The petroleum-derived waxes are comprised of one or more member selected from the group containing saturated n-alkanes, iso-alkanes, naphthenes, alkyl substituted aromatic compounds, and naphthene substituted aromatic compounds. Synthetic waxes can be polyethylene, Fischer-Tropsch waxes, chemically modified waxes or amide-modified waxes. Polyethylene waxes generally have the chemical formula C.sub.2H.sub.4).sub.nH.sub.2 and can have either linear chain or branched structures. The waxes can be based on ultra-high molecular weight polyethylene (UHMWPE) high-density polyethylene (HDPE), medium density polyethylene, linear low-density polyethylene (LLDPE), low-density polyethylene (LDPE) and very low density polyethylene (VLDPE). Fischer-Tropsch waxes generally have the chemical formula C.sub.nH.sub.(2n+2). Chemically modified waxes are converted from non-polar to polar molecules by the incorporation of functional groups such as hydroxyl, carboxyl, a salt, an ester and an acid group. Amide modified waxes have amide functional molecules grafted to the polyethylene chain to modify flexibility or adhesion or compatibility with other binder components.
(6) Ethylene copolymer is included in the thermoplastic composition to improve the flexibility, durability and flow modification of the pavement materials. Suitable examples include ethylene vinyl acetate copolymers, ethylene acrylate copolymers, ethylene methacrylate copolymers, ethylene acrylate glycidyl-acrylate copolymers. The amount of ethylene unit can range from 50% to 95% by weight and the remaining the other monomer in the copolymer. The preferred copolymer is ethylene-vinyl acetate. The vinyl acetate content can vary from 2% to 30% by weight in the copolymer.
(7) The compositions of this invention can comprise one or more fillers. Useful fillers are typically solids that are non-reactive with the other components of the compositions of this invention. The fillers constitute the major portion of the composition, comprising 70% to 85% by weight of the total composition. Useful fillers include clay, talc, glass particles and beads, metal oxide and sulfate particulates, ceramic microspheres, hollow polymeric or glass microspheres, carbonates, silica and aluminum trihydrate.
(8) The filler can include coloring pigments. Rutile titanium dioxide with a minimum purity of 92% is usually used for white materials and a combination of titanium oxide and organic or heavy metals free pigments is usually used for yellow materials. Barium sulfate or zinc oxide can also be used in place of titanium oxide in these compositions.
(9) The filler can also include ground calcium carbonate or magnesium carbonate with or without organic surface treatment. The particle size of these carbonates is selected based on the required flow characteristics of the thermoplastic composition.
(10) A glass fill can be used as a filler to provide viscosity modification.
(11) The particular glass beads used in the filler depend on the applicable governmental requirement for the size, quality, amount and retro-reflectivity. The glass beads provide continuous retro-reflectivity for extended periods compared to the paint based marking materials. As the marking materials wear, the glass beads in the composition are exposed, providing continued visibility for road markings.
(12) Bentonite clay is a special type of absorbent aluminum phyllosilicate, consisting mostly of montmorillonite. This clay has platelet morphology, with interstitial cations present in between the individual platelets. The usual cations are sodium, potassium and calcium. These clays swell in water to form colloidal dispersions. The property of swelling makes this clay useful as sealant, absorbent for organic materials, drilling mud for gas and oil exploration. This clay is modified with cationic organic surfactants to make it hydrophobic. The organic modified bentonites are used as additives in polymers to modify the mechanical and rheological properties. The organic modified bentonite clays are available commercially from BYK Additives Inc. (Gonzales, Tex.) and others.
(13) Preferably, the bentonite clay is compounded with the EVA or with the EVA and alkyd resin in the front end of an extruder. This combination is then compounded with the rest of the binder resin components and fillers to form a thermoplastic composition. The entire composition is extruded into a homogeneous molten mass, cooled down and cut into pellets.
(14) Preferably, the concentration of the bentonite clay is in the range of 0.01 to 5 weight percent of the thermoplastic composition, and more preferably in the range of 0.1 to 2 weight percent of the thermoplastic composition, and more preferably in the range of 0.5 to 1 weight percent of the thermoplastic composition.
(15) Because the bentonite clay minimizes the potential clumping of the pellets, there is no need to apply a calcium carbonate or other coating.
(16) Without being bound to any particular theory, it is believed that the bentonite clay disperses in the binder resin in an “exfoliated” mode, which increases the melt viscosity and reduces the resin flow. Additionally the nanometer thick clay sheets act as a diffusion barrier for the resin flow. The reduced resin flow eliminates pellets clumping under hot storage conditions.
(17) The present invention improves on the prior art coated pellets in other respects. The compositions made using this invention will eliminate the need to apply CaCO.sub.3 or other coatings after making the pellets. Thus, the present invention reduces the investment and operational costs for making the pellets. Moreover, the new composition will be dust-free, a feature much desired by the manufactures and the consumers. Finally, the invention permits the creation of a sizable inventory without concern to the storage condition at the plant or customer's facility or any abuse to the pellets during transportation.
Experiment 1
(18) Table 1 lists the ingredients for the preparation of the pellets used in the examples presented below.
(19) TABLE-US-00001 TABLE 1 Material description Alkyd resin Plasticizer and copolymer Titanium dioxide Calcium carbonate Glass beads Clay Calcined clay Bentonite clay
(20) AASHTO M249, T250 and California Department of Transportation (CALTRANS) test methods were used to characterize the thermoplastic compositions made using the ingredients in the given examples.
(21) The softening point of thermoplastic composition was measured using a ring and ball apparatus using ASTM method D36.
(22) The viscosity of the thermoplastic composition was measured using the CALTRANS method at 400° F. and 425° F. with a SC4-27 spindle. A Thermosel® disposable SC4-27 aluminum spindle and a Thermosel® disposable aluminum chamber were used for this measurement.
(23) The hardness of the thermoplastic composition was measured using a Type A Durometer at 115° F.
(24) The tendency of the thermoplastic pellets composition to clump under weight in hot storage conditions was evaluated using a “clumping” test method developed in-house. This method is a slight variation of another in-house developed method discussed in US Published Application No. US 2017/0158866 A1 to study the clumping of pellets at elevated temperature. A special silicone mold was made to make 1-inch diameter and 0.3 inch thick discs of the thermoplastic compositions. The silicone mold was made by drilling a series of one-inch diameter holes in a 0.3 inch silicone sheet, which was then bonded to another 0.3 inch silicone sheet using room temperature curable silicone adhesive. The discs were made by pouring the thermoplastic composition after heating to 425° F. and pouring the hot melt in the circular cavities in the silicone mold. After the melt cooled down to room temperature, the discs were removed.
(25) The smooth sides of two discs made using the above procedure were placed facing each other on a piece of smooth PVC block. A 2-inch long PVC tube with an inside diameter of 1.2 inches was positioned to keep the discs from sliding against each other during testing. A 2-inch long high-density polyethylene rod having a 1.1 inch diameter was placed on top of the discs assembly so that a half inch rod protrudes above the PVC tube. A 3-pound stainless steel cylinder was placed over the top of the polyethylene rod, so that the whole weight was squarely rested on the top of the discs without touching the PVC tube. The same experimental set up was duplicated three more times to test four sets of discs at the same time. The four test rigs were transferred carefully to an air circulating constant temperature oven maintained at 54° C. (129.2° F.) for 2.5 hours. The rigs were then removed from the oven, allowed to cool to room temperature. The discs bonded to each other strongly at the elevated temperature.
(26) After the rings cooled, ¾ inch aluminum dollies were attached to both sides of the bonded disc pair using Super Glue and cured overnight at room temperature. The dollies were connected to the instron equipped with 1000 pound load cell using quick connects. The dollies were pulled at a 0.2 inches/minute separation rate. The load at which the discs break was noted in pounds. The failure was usually at the interface of the two discs and not at the adhesive phase connecting the dolly and the pellet. The adhesive force measured was converted into force/unit area of the composition. The average of the four measurements was reported as “clump strength” for the particular test condition.
(27) Six thermoplastic compositions were prepared for analysis. A control example was prepared to which no clay was added to the composition. Two comparative examples were also prepared. Comparative Example 1 was modeled on the Control Example with 0.60 wt. % regular clay being added to the composition. Comparative Example 2 was modeled on the Control Example with 0.60 wt. % calcined clay being added to the composition.
(28) Three examples were also prepared based on the current invention. Example 1 was modeled on the Control Example with 0.20 wt. % bentonite clay being added to the composition. Example 2 was modeled on the Control Example with 0.40 wt. % bentonite clay being added to the composition. Example 3 was modeled on the Control Example with 0.60 wt. % bentonite clay being added to the composition.
(29) The compositions of the Control Example, both Comparative Examples and all 3 Examples of the invention are presented in Table 2 below.
(30) TABLE-US-00002 TABLE 2 Control Comparative Comparative Example Example Example Ingredients Example Example 1 Example 2 1 2 3 ′Maleic anhydride 18.26 18.26 18.26 18.26 18.26 18.26 modified ester resin Plasticizer and 8.24 8.24 8.24 8.24 8.24 8.24 copolymer Titanium dioxide 10.00 10.00 10.00 10.00 10.00 10.00 Calcium carbonate 26.00 26.00 26.00 26.00 26.00 26.00 Glass beads 37.50 36.90 36.90 37.30 37.10 36.90 Clay None 0.60 0.60 0.20 0.40 0.60 Regular clay Calcined clay Bentonite Bentonite bentonite clay clay clay
(31) The properties of each of the 6 compositions were measured using the procedures outlined above. The results of those measurements are presented in Table 3 below:
(32) TABLE-US-00003 TABLE 3 Control Comparative Comparative Example Example Example Properties Example Example 1 Example 2 1 2 3 Softening point (° F.) 229 229 229 230 231 232 Melt viscosity At 400° F. 60 rpm 2883 2954 2850 2983 3458 3821 30 rpm 3467 3625 3667 3558 4200 4767 12 rpm 4813 5854 5583 5500 6146 7188 6 rpm 6708 9083 8375 7458 8625 10292 At 425° F. 20 rpm 3500 3550 3638 3813 4262 4912 Hardness 68 70 72 82 88 85 Clump strength (psi) At 45° C. 21.1 20.4 20.7 18.2 20.3 20.7 At 54° C. 151.9 146.1 142.6 77.0 49.2 47.9
(33) The addition of bentonite clay in small quantities does not affect the softening point of the thermoplastic composition. The bentonite clay increased the melt viscosity and hardness of these compositions. Unexpectedly the “clump strength” at higher temperatures decreased substantially with the addition of a small amount of bentonite clay in the thermoplastic compositions. Notably, the clump strength did not decrease when adding regular clay or calcined clay to the composition. This reduction in the “clump strength” demonstrates that the thermoplastic pellets containing bentonite clay will have an improved resistance to clumping as compared with standard pellets and pellets containing other clays.
Experiment 2
(34) In a further experiment, a thermoplastic composition containing bentonite clay but no other viscosity modifiers was compared with a thermoplastic composition without bentonite but containing other viscosity modifiers. The bentonite not only improves resistance to pellet clumping, but it also modifies the melt viscosity profile and prohibits settling of the glass beads and fillers at the striping application temperature.
(35) The tendency for a given formulation to prohibit bead/filler settling was evaluated by allowing the melts from Experiment 2 to cool, undisturbed, in the aluminum viscosity thimbles immediately after measuring their melt viscosity profiles. Once the thimbles were cooled to room temperature, the thimble was bisected into a top and bottom portion with a diamond saw. Each top and bottom portion of the thermoplastic sample was removed and evaluated for binder content and glass bead and filler content according to AASHTO test method T250. The difference in the amount of glass beads and filler between the top and bottom portions of the bisected samples is a direct measurement of the ability of the formulation to prevent bead and filler settling. Table 4 below summarizes the improved performance for formulations containing bentonite.
(36) TABLE-US-00004 TABLE 4 Composition with glass- fill and no bentonite and Composition with glass- Control Composition no other viscosity fill and bentonite and no Ingredients with glass-fill modifiers other viscosity modifiers Maleic anhydride 14.86 18.86 18.86 modified ester resin Plasticizer + co-polymer 5.94 1.94 1.94 Bentonite 0 0 0.5 TiO.sub.2 10 10 10 CaCO.sub.3 filler 1.5 1.5 1.5 Glass beads 32.5 32.5 32.5 Glass fill 35.2 35.2 34.7 Melt viscosity at 400° F. 60 rpm EEEE EEEE EEEE 30 rpm 6683 7908 EEEE 12 rpm 8979 8854 9417 6 rpm 12500 10042 11125 at 425° F. 20 rpm 5887 4787 5500 10 rpm 8150 6300 7025 As Formulated Binder 20.80% 20.80% 20.80% Glass beads 32.5% 32.5% 32.5% Glass fill 35.2% 35.2% 34.70% Binder content % as measured Bottom half 17.64 16.99 18.44 Top half 22.14 21.81 21.83 Glass beads/glass-fill as measured Bottom half 66.46 67.13 61.37 Top half 58.06 56.23 56.17 Glass bead/glass-fill 8.4 10.9 5.2 settling (bottom-top)
(37) The use of bentonite in the formulation of Experiment 2 results in an improved thermoplastic product with an increased resistance to filler and/or glass bead settling, as compared to the control composition. The control composition, which contains viscosity modifiers but no bentonite, also performs much better than a formulation with no viscosity modifiers. The formulations from Experiment 2 and similar formulations can be produced as a powdered or pelletized product.
(38) Various modifications and alterations to this invention will become apparent to those skilled in the art. The amount of bentonite in the thermoplastic composition can be adjusted to modify the “clump” force, suitable to avoid clumping of the pellets in any adverse storage conditions.
(39) While the above description contains certain specifics, these should not be construed as limitations on the scope of the invention, but rather as an exemplification of one preferred embodiment thereof. Accordingly, the scope of the present invention should be determined not by the embodiment(s) illustrated, but by the appended claims and their legal equivalents.