TECHNICAL BACKGROUND Filled plastics, and various methods for their manufacture constitute a well developed art. Especially, articles formed from these filled plastics via injection molding and subsequent cross-linking of the polymeric matrix comprise a large body of commercially useful products. Often, articles of manufacture are comprised of a thermoplastic or thermosetting polymeric matrix and an inert filler, such as calcium carbonate, calcium sulfate, calcium silicate, silica, clay, calcined alumina, alumina trihydrate, spheres, talc, kaolin, feldspar, baryte, mica, calcium sulfate, hollow glass spheres, ceramic materials, carbon black or carbon fiber. Other filler materials include nylon flock fibers, and polyester fibers. Articles of manufacture comprising polymeric methyl methacrylate homopolymer and an alumina trihydrate filler are disclosed in U. S. Pat. No. 3,084,068, Re. 27,093, 3,847,865 and 4,107,135.

Among the uses of these filled plastics are decorative solid surfacing materials such as simulated marble, kitchen sinks, bathroom sinks, table tops, counter tops, dresser tops, vanity tops, shelving, and furniture applications. Depending on the severity of these applications, properties such as toughness, temperature resistance, scratch resistance, microbial resistance, translucency, and flame resistance of the laminate surface are very important. Most of these decorative surface materials are manufactured with poly (methyl methacrylate) (hereinafter referred to as PMMA) as a matrix material with different inert fillers.

PMMA offers excellent optical clarity (92% of white light) and brilliance. It remains unaffected by most household detergents, cleaning agents and solutions of inorganic acids, and alkalis. Moreover, it is

amenable to forming shapes via injection molding, extrusion, and polymerization casting.

Like most other thermoplastics, PMMA exhibits a higher coefficient of thermal expansion as compared to metals. However, the most significant disadvantage of PMMA is that its thermal properties limit its use in articles. PMMA softens circa. 115°C and its continuous service temperature is lower, approximately 95°C. Therefore, other plastic materials are used in high temperature applications. In the specific usage of decorative sheets and related articles, three limitations are observed in high performance applications: (i) ineffective ability to withstand higher temperature conditions (in the range of 100°C through 200°C), (ii) lower material hardness of materials with a PMMA matrix and (iii) lower scratch and mar resistance of such materials. Thus, polymeric matrix materials with good temperature resistance and/or scratch resistance and/or higher flexural modulus are desired.

In the manufacture of such filled plastic articles such as decorative surfaces, monomer volatility can be an environmental hazard issue. A lower volatility monomer is usually desired.

Since the refractive index of the fillers is usually high, a closer match of the refractive index of the polymer to the matrix, while preserving other properties such as clarity and weatherability is desired to create materials with a greater translucency.

Copolymers of an alpha-methylene gamma-butyrolactone (hereinafter referred to as a-MBL) with various vinyl monomers are known in the literature (Kunstoffe, 87, pp 734-736,1997; incorporated herein by reference). Making copolymers from methyl methacrylate or other monomers and an exomethylene lact (one) (am) monomer is described in U. S. Pat. 5,880,325.

British patent 614,310 and U. S. Pat. 2,624,723 describe the synthesis of methylene lactone homopolymers. The British patent also mentions the possibility of additives such as fillers and coloring materials to modify the homopolymer properties. Patents US 3,847,865, US Re.

27,903 and US 4,107,135 describe a process where a decorative surface can be formed using PMMA as the matrix or its copolymers as the matrix, for example, ethylenically unsaturated compounds as co-monomers.

These patents teach how to fabricate decorative sheet with a polymer matrix and a filler such as calcium carbonate, alumina trihydrate, nylon fiberstock, polyester fiber, silica, spheres, talc, kaolin, feldspar, baryte,

mica, calcium sulfate, hollow glass spheres, ceramic materials, carbon black or carbon fiber.

SUMMARY OF INVENTION This invention concerns a composition comprising, a copolymer of at least one a-methylene lact (one) (am) monomer of formula (I) and at least one other free radically copolymerizable monomer, and an inorganic filler, provided that no more than 95 mole percent and not less than 1 mole percent of repeat units in said copolymer are derived from said a- methylene lact (one) (am) monomer, wherein: n is 0, 1 or 2 ; X is-O-or-NR9- ; and R1, R2, R5, and R6 each of R3 and each of R4, are independently hydrogen, a functional group, hydrocarbyl or substituted hydrocarbyl, and R9 is independently hydrogen, or hydrocarbyl or substituted hydrocarbyl.

This invention also concerns, a composition, comprising an a- methylene lact (one) (am) homopolymer, and between 5% and 80% by weight of a filler, based on a total weight of said homopolymer, and said filler.

This invention also concerns a composition comprising an a- methylene lact (one) (am) copolymer and between 5% and 80% by weight of a filler, based on a total weight of said copolymer and said filler.

This invention also concerns a composition comprising an a- methylene lact (one) (am) homopolymer, and at least 10% by weight of alumina trihydrate based on a total weight of said homopolymer and said alumina trihydrate.

This invention also concerns a composition comprising an a- methylene lact (one) (am) copolymer and at least 10% by weight of alumina trihydrate based on a total weight of said copolymer, and said alumina trihydrate.

This invention also concerns a composition comprising at least one a-methylene lact (one) (am), a free radically copolymerizable monomer and an inorganic filler. This composition can optionally include a free radical initiator.

This invention also describes a process for manufacturing a plastic article, comprising contacting, (a) one or more acrylate or methacrylate esters (b) one or more a-methylene lact (one) (am) monomer of the formula (I) wherein: n is 0,1 or 2 ; X is-O-or-NR9- ; and RI, R2, R5, R6, each of R3 and each of R4, are independently hydrogen, a functional group, hydrocarbyl or substituted hydrocarbyl, and R9 is a hydrocarbyl or a substituted hydrocarbyl, (c) at least one free radical initiator, (d) at least 10 weight percent of a filler based on total weight of the said homopolymer or copolymer and the filler, (e) optionally, one or more homopolymers or copolymers of acrylate and/or methacrylate esters, provided that said contacting is at a sufficient temperature to cause said free radical initiator to generate free radicals; and (b) is at least 1 mole percent of the total of (a) and (b).

This invention also describes a process for manufacturing a plastic article, comprising contacting, (a) one or more acrylate or methacrylate esters (b) one or more a-methylene lact (one) (am) monomer of the formula (I)

wherein: n is 0, 1 or 2 ; X is-O-or-NR9- ; and R1, R2, R5, R6, each of R3 and each of R4, are independently hydrogen, a functional group, hydrocarbyl or substituted hydrocarbyl, and R9 is a hydrocarbyl or a substituted hydrocarbyl, (c) at least one free radical initiator, (d) at least 10 weight percent of alumina trihydrate based on total weight of the said homopolymer or copolymer and alumina trihydrate, (e) optionally, one or more homopolymers or copolymers of acrylate and/or methacrylate esters, provided that said contacting is at a sufficient temperature to cause said free radical initiator to generate free radicals ; and (b) is at least 1 mole percent of the total composition of (a) and (b).

DETAILED DESCRIPTION OF THE INVENTION The following terms as used herein are defined below : By"hydrocarbyl group"is meant a univalent group containing only carbon and hydrogen. If not otherwise stated, it is preferred that hydrocarbyl groups (and alkyl groups) herein contain about 1 to about 30 carbon atoms.

By"substituted hydrocarbyl"is meant a hydrocarbyl group which contains one or more substituent groups which are inert under process conditions to which the compound containing the group is subjected. The substituent groups also do not substantially interfere with the process. If not otherwise stated, it is preferred that substituted hydrocarbyl groups herein contain 1 to about 30 carbon atoms. Included in the meaning of

"substituted"are heteroatomic rings. In substituted hydrocarbyl all of the hydrogens may be substituted, as in trifluoromethyl.

By"functional group"is meant a group other than hydrocarbyl or substituted hydrocarbyl which is inert under the process conditions to which the compound or polymer containing the group is subjected. The functional groups also do not substantially interfere with any process described herein that the compound or polymer in which they are present may take part in. Examples of functional groups include halo (fluoro, chloro, bromo, and iodo), and ether groups such as-OR22 wherein R22 is hydrocarbyl or substituted hydrocarbyl.

By"copolymerizable under free radical conditions"is meant that the monomers involved are known to copolymerize under free radical polymerization conditions. Preferably, the monomers involved are vinyl monomers. The free radicals may be generated by any of the usual processes, for example thermally from radical initiators such as peroxides or azonitriles, by UV radiation using appropriate sensitizers etc., and by ionizing radiation. The copolymerization may be done in any number of known ways, for example bulk and solution polymerization. These polymers may be prepared by various types of processes, such as continuous, batch and semibatch, which are well known in the art. Many combinations of free radically copolymerizable monomers are known, see for instance J. Brandrup, et al., Ed., Polymer Handbook, 4th Ed., John Wiley & Sons, New York, 1999, p. ll/181-ll/308.

By"copolymer of a-methylene lact (one) (am)" is meant that at least 1 mol % of the repeat unit in the copolymer are derived from the homopolymer of an a-methylene lact (one) (am) of the general formula wherein X and R1 through R6 and R9 are as defined above. In a preferred structure of I and corresponding polymeric repeat units: n is 0; and/or

R1, R2, R3, R4, R5 and R6 are hydrogen or alkyl containing 1 to 6 carbon atoms, more preferably all are hydrogen; and/or X is-O-or-NR9-wherein R9 is hydrogen or alkyl containing 1 to 6 carbon atoms, more preferably X is-O-.

By"inorganic filler"is meant a finely divided inorganic material which may cause property changes to the final article into which it is incorporated. Examples of inorganic fillers are calcium carbonate, calcium sulfate, calcium silicate, silica, clay, calcined alumina, alumina trihydrate, glass fibers, carbon fibers, titanium dioxide, spheres, talc, kaolin, feldspar, baryte, mica, hollow glass spheres, ceramic materials, and carbon black.

Decorative solid surface materials may be manufactured using a PMMA matrix and an inorganic filler, with appropriate coupling agents, initiators, etc. However, several properties of the decorative surface materials and sheets can be improved to better serve their application purpose. Herein, the properties of the composition with higher toughness and hardness improve scratch and impact resistance. A higher temperature resistance can expand the utility of the articles, for example, kitchen countertop applications would benefit from improved temperature resistance. Localized heating of the surface in table and kitchen tops can be very high when a hot object in placed on it. A polymer having a higher glass transition temperature (Tg) in this situation can help reduce damage to the surface.

The properties of the composition are improved herein by improving the matrix polymer. Described is a product and process for fabrication from a composition to give the matrix material which is a copolymer of a- methylene lact (one) (am) and an inert filler.

The a-methylene lact (one) (am) repeat unit (s) in the copolymer composition is (are) derived from the monomer

wherein X and RI through R6 are as defined above. In a preferred structure: n is 0; and/or RI, R2, R3, R4, R5 and R6 are hydrogen or alkyl containing 1 to 6 carbon atoms, more preferably all are hydrogen; and/or X is-O-or-NR9-wherein R9 is hydrogen or alkyl containing 1 to 6 carbon atoms, more preferably X is-O-.

In a particularly preferred structure, n is 0, X is-O-and RI, R2, R5 and R6 are hydrogen, or n is 0, X is-O-, R6 is methyl, and RI, R2 and R5 are hydrogen. This structure is also known as a-methylene-y- butyrolactone. For other preferred structures, see U. S. Patent 5,880,235, which is hereby included by reference, at column 4, line 44 to column 8, line 59.

The free radically copolymerizable monomer in the composition of the copolymer may have the formula wherein R14 is hydrogen or methyl, and R15 is hydrocarbyl or substituted hydrocarbyl, preferably alkyl, R16 is hydrogen or methyl and R17, R18, R19 R20 and R21 are each independently hydrogen, hydrocarbyl substituted hydrocarbyl or a functional group. In a preferred (II), R14 and R15 are both methyl (methyl methacrylate), and in a preferred (III), R16, R17, R18, R19 R20 and R21 are all hydrogen (styrene). In another preferred copolymer, these repeat units are derived from methyl methacrylate and an alkyl acrylate, preferably ethyl acrylate. The free radically copolymerizable monomer may also include acrylonitrile, acrylic acid or or methacrylic acid.

Fillers of the invention can include, but are not limited to, one or more of the following :

Aluminum Hydroxide Barium Hydroxide Oxide Oxide Sulfate Sulfate Phosphate Phosphate Silicate Silicate Calcium Sulfate Magnesium Sulfate Silicate Silicate Phosphate Phosphate Carbonate Hydroxide Hydroxide Oxide Apatite Glass Bubbles Clays Kaolin Microspheres Montmorillonite Fibers Bentonite Beads Pyrophyllite Flakes Powder Additional : Mica Cristobalite Powder Talc Wood flour Gypsum Feldspar Titanium Dioxide Carbon black Quartz Zircon Diatomaceous earth Borax Silica Wollastonite Calcite Carbon fiber Ceramic Microspheres Calcined alumina Baryte In a preferred composition, an inorganic filler may be a mixture of alumina trihydrate with any of the other inorganic fillers listed here. In a particularly preferred composition, inorganic filler is alumina trihydrate.

The filler can also be an organic filler which includes, but is not limited to nylon fiber, polyester fiber.

A preferred content of the filler is about 5% to about 80% by weight of the total article. In a more preferred combination, the filler content is in the range of about 40% to about 60% by weight. A preferred content of

the polymer in the final article is about 40% to about 60%, by total weight of the polymer and alumina trihydrate.

A preferred content of alumina trihydrate filler is about 10% to about 80% by weight of the total article. In a more preferred combination, the alumina trihydrate content is in the range of about 40% to about 60% by weight. A preferred content of the polymer in the final article is about 40% to about 60%, by total weight of the polymer and alumina trihydrate.

The a-methylene lact (one) (am) repeating unit weight content in the total polymer present in the composition is preferred in the range of about 1 % to about 95%, preferably about 30% to about 40% of the total polymer weight, with a preferable minimum amount of about 2% or a more preferable minimum amount of about 5% or a more preferable amount of about 10% or a further preferable amount of about 20% and preferable maximum amount of about 80% or a more preferable maximum amount of about 65% and a further preferable maximum amount of about 50% and a more preferable amount of about 40%, such that any preferable minimum amount can be combined with any preferable maximum amount.

The content of the repeat units derived from the free radically copolymerizable monomer (s) is preferred from about 5% to about 99%; more preferably about 60% to about 70% of the copolymer. In a preferred composition, the free radically copolymerizable monomer is methyl methacrylate. In another preferred composition, the free radically copolymerizable monomers are methyl methacrylate and an alkyl acrylate, wherein the alkyl group has 1-8 carbon atoms, more preferably ethyl acrylate or n-butyl acrylate, and/or the alkyl acrylate content is not more than about 10 mole % of the radically copolymerizable comonomer content. It is also possible to use glycidyl acrylate or methacrylate in any of the above compositions. In a particularly preferred composition, the free radically copolymerizable monomer may be a mixture of methyl methacrylate and ethyl or butyl acrylate, where the ethyl or butyl acrylate content is not more than about 5 weight % of the radically copolymerizable comonomer content in the final copolymer matrix. Such copolymers are described in U. S. Patent 5,880,235, which is hereby incorporated by reference.

When an a-methylene lact (one) (am) is present in a copolymer, it tends to raise the glass transition temperature (Tg). For example, in a copolymer with methyl methacrylate, the Tg will normally be above the Tg of a PMMA homopolymer.

A preferred composition useful for a decorative sheet is a copolymer of at least one of a-methylene lact (one) (am) monomer and at least one of the alkyl acrylate monomer with at least 30 weight % inorganic filler, from one or more of the inorganic fillers listed previously. A particularly preferred composition is a copolymer matrix of a-methylene-y- butyrolactone, and methyl methacrylate or a copolymer of a-methylene-y- butyrolactone and ethyl acrylate, with at least 10 weight percent of alumina trihydrate filler.

Another type of monomer that may be used is a monomer that contains more than one polymerization sites for e. g., a di-or tri-acrylate, or methacrylate, or vinyl styrene. During the polymerization, these monomers cause crosslinking of the polymer. Usually, relatively small amounts are added so that the monomer is not highly crosslinked.

Included in the composition herein are those compositions where PMMA or another homo-or copolymer is present in the composition which are a mixture of PMMA or a copolymer of PMMA and alkyl acrylate.

Decorative sheet compositions described herein usually have better thermal resistance compared to a composition made with a pure PMMA, see for instance Table 1 in Example 3, where the glass transition temperatures of a-MBL polymer, of PMMA and of copolymers of a-MBL and MMA are given.

Another advantage that copolymerization of a-methylene lactone often imparts to the decorative sheet manufacture process is the high rate of chemical reaction (also known as cure rate). Table 1 also lists the time in minutes taken to achieve the highest temperature of reaction, by polymeric matrices with varying a-methylene lactone contents.

Table 3 in Example 3 gives experimentally determined modulus of elasticity properties. An improvement in modulus of elasticity is found with an increasing a-methylene lactone content.

Filled polymer compositions described herein have a better refractive index match between the polymer and the filler due to the higher refractive index of poly (MBL) compared to PMMA. This can result in materials with a greater translucency.

All of the compositions herein may additionally comprise other materials commonly found in thermoplastic compositions, such as, dyes, pigments, UV stabilizers, processing aids, flame retardants, antioxidants, and antiozonants. These materials may be present in conventional

amounts, which vary according to the type (s) of material (s) being added and their purpose in being added.

It was found that incorporating the compositions of this invention into a solid surface material caused the solid surface material to exhibit antimicrobial/antibacterial properties. The antimicrobial/antibacterial effectiveness was tested with Escherichia Coli bacteria in a residual self- sanitizing test. Example 8 demonstrates that a-MBL-based decorative sheet reduced the bioburden by 3.92 logs, or greater than 99.9% reduction of bacteria as compared to the control sheet. For purposes of antimicrobial/antibacterial activity, the compositions of this invention can be incorporated into a wide array of products, such as, bathroom vanity tops, sinks, shower stalls, kitchen counter tops, solid surfaces in hospitals, nursing homes and daycare facilities, commercial and residential food preparation facilities, office supplies, and other applications where it is desirable to minimize human contact with bacteria.

EXAMPLES In the Examples the following abbreviations are used: VAZO@ 67-azobis (methylbutyronitrile) DMSO-dimethyl sulfoxide MMA-methyl methacrylate a-MBL-a-methylene-y-butyrolactone Tg-glass transition temperature DMA-dynamic mechanical analysis ATH-alumina trihydrate GDMA-Glycol dimercaptoacetate PMMA-Poly (methyl methacrylate) TSAX-TrypticaseE Soy Agar TSBO-Trypticase@ Soy Broth MMA was obtained from Aldrich Chemical Company, Inc., Milwaukee, Wi, U. S. A. AIBN, ZonyltD UR fluorosurfactant external release coating were obtained from E. I. du Pont de Nemours & Co., Wilmington, DE, U. S. A. Silastic@ gasket (silicone rubber) was obtained from Dow Corning Corp., Midland, MI, U. S. A. t-butyl peroxyneodecanoate was obtained at a 25 wt% dispersion in mineral oil (Lupersol0 10M75) from Atofina, King of Prussia, PA. The TrypticaseSsoy broth and agar were obtained from Becton, Dickinson Biosciences of Franklin Lakes, NJ.

Haze and transmission were measured according to ASTM D1003.

The flexural modulus was measured by ASTM D790. DMA measurements were performed by ASTM 5023 with torque force of 1.2-1.4 N m. The bar was scanned in 5 frequencies (0.3,1,3,10 and 30 Hz) at 1°C/min rate from-140°C to 180°C. The oscillation amplitude was 10, um. Glass transition temperatures (Tg) were measured by ASTM D3418 at a heating rate of 10°C/min and the Tg was measured as the midpoint of the transition.

EXPERIMENT 1 Preparation of filled sheet (thermal cure) The following ingredients are added to a 1000 mL reaction kettle, fitted with a temperature probe, air-driven stirrer, rubber septum and a reflux condenser: trimethylolpropane trimethacrylate 4.48 g 10% solution of poly (methyl methacrylate-co-ethyl acrylate 96/4) in MMA 492.84 g Pigment paste 0.53 g t-butyl peroxyneodecanoate, 25% dispersion in mineral oil 1. 79 g VAZO 67 0.36 g After mixing these ingredients, 500 g of ATH were added portionwise over a two minute interval. During the portionwise addition of the ATH, the stirring speed was increased to about 1500 rpm.

After the ATH addition was complete, the stirring speed was increased to 2000 rpm and maintained for 10 min. About 2.5 g of MMA monomer was added and the mix was then evacuated at 100 Pa for two min. with 1000 rpm stirring. The mixture was poured into a casting mold constructed from two stainless metal plates (25.4 cm x 25.4 cm x 1.0 mm) separated by a SilasticE gasket (12.95 mm thickness). Each of the metal plates was coated with a ZonylE UR external release coating. The casting mold was assembled using spring clamps. After bleeding a small amount of air from the cell, the sealed cell was submerged vertically in an 80°C waterbath. Twenty min. later, the casting cell was removed from the waterbath and placed in a 120°C circulating hot air oven for 60 min.

EXAMPLE 1-3 Preparation of filled sheet containing a-methylene a-butvrolactone (thermal cure) Three polymer syrups of 10 weight % solution of poly (methyl methacrylate-co-ethyl acrylate) (96/4 weight percent) in a MBL/MMA mixtures were made by slowly dissolving the polymer in the monomer in a reaction kettle. In the 100 % MBL mixture, no acrylic odor was observed, nor was there any foaming or bubbling in the degassing step. These syrups were used to make filled acrylic sheet as described in Experiment 1. The color of these sheets was similar to the sheet of Experiment 1.

Table 1: Time in minutes taken to achieve the highest temperature of reaction and Ta of MBL/MMA filled sheet (thermal cure) Example MBL/MMA Time to peak Tg (°C) (Wt%) temperature (min) 1 100/0 4.5 min 177 2 50/50 4.5 min 148 3 27/75 9.5 min 122 Table 2: Properties of MBL/MMA fitted sheet (thermal cure) Property ASTM MMA MBL filled sheet filled sheet Example 1 Ultimate stress MPa ASTM D790 58.2 51.3 Ultimate strain % ASTM D790 2.26 0.503 Energy to break N. m ASTM D790 0.411 0.061 Elastic modulus GPa ASTM D790 6.46 10.70 Table 3: DMA data on MBL/MMA fitted sheets (thermal cure) Thermal Example 1 Example 2 Example 3 100% PMMA Properties cured Modulus E'10. 4 GPa 8.2 GPa 7.9 GPa 7.4 GPa @25°C Ta @1 Hz by 122.0°C 77°C, 105°C 93°C 107°C DMAE"peak Tß @1 Hz by 61. 1°C, Eact = 2. 0°C, Eact = 12. 0°C. Eact = 16. 8°C, Eact= DMA E"peak 96 kcal/mole 20.9 kcal/mole 19 kcal/mole 18 kcal/mole Té'@1 Hz by 2.6°C, Eact = DMA E"peak 26 kcal/mole Ty@1Hzby-100°C, Eact=-102°C, Eact=-105°C, Eact= DMA E"peak 13 kcal/mole 14 kcal/mole 13 kcal/mol

Ta is the highest relaxation temperature corresponding to the glass transition, To and Tp'are the next lowest relaxation temperatures believed to be from the lactone ring motion, Ty is the lowest observed relaxation temperature believed to be the motion of-CH3.

EXAMPLE 4 Preparation of filled sheet containing methylene butyrolactone (chemical cure, MBL 10 weight % of available monomer) The following ingredients were sequentially added to a 2000 mL reaction kettle, fitted with a temperature probe, air-driven stirrer, rubber septum and a reflux condenser: t-Butyl peroxymaleic acid 9.81 g Pearl grey pigment paste 0.91 g Dioctyl sodium sulfosuccinate 3.92 g Trimethylolpropane trimethacrylate 6.54 g MMA 56.22 g a-MBL 52.96 g 24% solution of poly (methyl methacrylate) in MMA 544.6 g After mixing these ingredients for 1 min at room temperature, 1020 g of ATH were added portionwise over a 2 min interval and then stirred for 10 min.

About 5.0 g of MMA was added. The mix was then evacuated at 10 KPa with stirring. Vacuum was lowered to 20 KPa with stirring, then gently warmed to 40°C using a waterbath. The following ingredients were sequentially injected in rapid succession: Demineralized water 2.04 g Calcium hydroxide dispersion in butylmethacrylate monomer 2.81 g Glycol dimercaptoacetate (GDMA) 1.43 g The addition of the GDMA was considered the starting point in time of experiment. The slurry was mixed at 41 °C for 10 s. Mixing was discontinued and the vacuum released and poured into a 12.6 mm tilted adiabatic casting mold.

EXAMPLE 5 Preparation of filled sheet containing methylene butvrolactone (chemical cure, MBL 20% of available monomer) The recipe of Example 4 was repeated with the following changes only : MMA 3.26 g MBL 105.92 g EXAMPLE 6 Preparation of filled sheet containing methylene butyrolactone (chemical cure, MBL 5% of available monomer) The recipe of Example 4 was repeated with the following changes only : MMA 82.70 g MBL 26.48 g EXAMPLE 7 Preparation of filled sheet containing methylene butvrolactone (chemical cure, MBL 15% of available monomer) The recipe of Example 4 was repeated with the following changes only : MMA 29.74 g MBL 79. 44 g Table 4: Time in minutes taken to achieve the highest temperature of reaction and Tg of MBL/MMA filled sheet, chemical cure. Example MBL/MMA Wt% Peak Time to achieve TemperaturePeak °C (+/-2°C) Temperature (+/- 0. 5 min) 6 5/95 129 13 min 4 10/90 131 10. 5 min 7 15/85 133 7 min 5 20/80 133 6 min Table 5: Properties of MBL/MMA filled sheet, chemical cure (ASTM D790) Property PMMA sheet Ex 4 Ex 6 Ex 7 Ultimate stress MPa 79.8 67.7 67.6 66.8 Ultimate strain % 1.06 0.88 0.90 0.83 Energy to break J 0. 441 0. 315 0.311 0.284 Elastic modulus GPa 9.46 9.57 8. 99 9.57

EXAMPLE 8 Antimicrobial activitv of oc-MBL filled sheet MBL filled acrylic sheet from Example 1 was cut in 5x5 cm tiles.

Corian0 control pieces were 6x6 cm. The test organism was Escherichia coli, ATCC #25922. The inoculum was prepared by diluting an overnight culture (grown in Trypticase@ Soy broth) 1: 1,000 (v/v) in dilute phosphate buffer. All polished surfaces of the tiles were wiped with isopropyl alcohol and cheesecloth to clean the surface. A 0.5 mL aliquot of the inoculum was pipette and spread over the surface of each Coran0 tile and a 0.42 mL aliquot was spread over the surface of each MBL tile. The inoculated tiles were each placed in a closed, sterile glass petri plate and placed in open fiberglass trays. The samples were incubated at 25°C and 85% RH. At the end of the incubation time, the tiles were washed twice with enough sterile phosphate buffer to bring the combined inoculum and wash buffer to 10 mL. The tiles were then wiped dry with a piece of sterile gauze to ensure that the inoculum was wiped completely from the tile.

The viable bacteria were then enumerated using a standard serial-dilution spread-plating technique on Trypticase@ soy agar (TSA). The lower limit of detection with this method is 1.0 x 1 o2 CFU/mL (Colony Forming Units per milliliter). The maintenance of antimicrobial activity of the tiles is expressed as the At value where, At=log CFU/mL of control tile-log CFU/mL of test tile (both at the same exposure time) The MBL tiles demonstrated significant antibacterial activity in 5h of exposure to E. coli and reduced the bioburden by 3.92 logs (>99.9% reduction) compared to the Coran0 control.