CA2163390A1 - Flexible reflective material and process for making the same - Google Patents

Flexible reflective material and process for making the same

Info

Publication number
CA2163390A1
CA2163390A1 CA002163390A CA2163390A CA2163390A1 CA 2163390 A1 CA2163390 A1 CA 2163390A1 CA 002163390 A CA002163390 A CA 002163390A CA 2163390 A CA2163390 A CA 2163390A CA 2163390 A1 CA2163390 A1 CA 2163390A1
Authority
CA
Canada
Prior art keywords
layer
polymer
substrate
acrylic
rollers
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002163390A
Other languages
French (fr)
Inventor
Russell C. Fellows
Phillip R. Davis
Samuel M. Madonian
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CA002163390A priority Critical patent/CA2163390A1/en
Publication of CA2163390A1 publication Critical patent/CA2163390A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/16Articles comprising two or more components, e.g. co-extruded layers
    • B29C48/18Articles comprising two or more components, e.g. co-extruded layers the components being layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin

Abstract

A flexible reflective material substantially free from optical chatter having a reflective layer adjacent to a substrate layer comprising a polyester. The refle ctive layer is preferably constructed of metallic particles disposed on a translucent polyme r layer, and the substrate layer is preferably a glycol modified polyethylene terephthala te. The reflective layer can also have an acrylic layer therein. Also, a process of maki ng a flexible multi-layered polymer material is provided comprising heating a polymer to at least its melting point, extruding the polymer between a first and a second cyli ndrical roller, each maintained at selected temperatures and positioned a selected dista nce apart while rotating in synchronization. A laminate layer is supplied under tension to the rollers along with the molten polymer, and the laminate layer and polymer are co mbined under a selected high pressure to form a multi-layered polymer product.

Description

- ~163390 Attorney Docket No.: 1691.001 FLEXIBLE REFLECTIVE MATERIAL
AND PROCESS FOR MAKING TIIE SAME

BACKGROUND OF T~E INVENTION

The present invention relates to the field of reflective polymer products, and methorls of m~nllfactllring the same. In particular, the present invention provides a low cost altemative to tr~ition~l glass mirrors, and may be formed into a variety of useful 10 and orn~m~ont~l shapes.

BACKGROUND OF T~E rNVENTlON

P~epl~cem~nt reflective products are increasingly desirable to ~limin~te the cost, - weight, and potential danger of traditional mirrored glass. Additionally, plastic reflective products that can be molded into useful articles, such as p1ates or automobile vent shades, are h~cleasingly sought. Such alternative reflective products currently available are frequently constructed of chrome materials or with metallic particles embedded in a polymer base. Although desirably light-weight, the currently available reflective polymer products do not provide a satisfactory reflective image. The appearance of prior art reflective polymer products is relatively dull and characterized by Attorney Docket No.: 1691.001 2 transverse optical chatter lines or waves that distort the reflective image. Available reflective polymer products are not snfficiently flexible to resist cracking. DeiAminAtion of polymer layers is also a common problem with existing reflective products. In addition, current reflective polymer products are not moldable to s~tisf~ctory dimen~;ons 5 without thinning or splittin~ into unusable forms or beco.,.in~ so,,,c~l~l cloudy in appearance. These shortcomings in the prior art are due to the currently available compositions of reflective particles and polymer substrates, as well as ~nC~ ctory means for mAnllfActuring such products.

Consequently, there is a need in the art for a flexible reflective polymer material that is substantially free from optical chatter to provide an undistorted reflective image.
There is also a need for a flexible reflective product that is stronger than other known compositions and can, therefore, be molded into usefi~l forms without splitting or del~l.linAl;on. Furthermore, there is a need in the art for improved methods of 15 mAnuf~ctllring such a flexible reflective material.

- - 21633~

Attorney Docket No.: 1691.001 3 SUMMARY OF TIIE lNVENTlON

The present invention provides a flexible reflective material s~ lly free from optical chatter. The invention provides such a material having a reflective layer 5 adjacent to a substrate layer comprising polyethylene te~tph~ lq-te. The reflective layer is pref~-ably constructed of metallic particles disposed on â tran~Uc~nt polymer layer, and the substrate layer is p~efe.ably a glycol modified polyethylene te.~ph~ qte The reflective layer can also have an acrylic layer therein.

The invention also provides a process of making a flexible multi-layered polymer material comprising heating a substrate polymer to at least its melting point, extruding the polymer between a first and a second cylindrical roller, each .. ~ i ed at selected temperatures and positioned a selected ~listqnce apart while rotating in sy~.c~"oni~alion.
A lqminqte layer is supplied under tension to the rollers along with the molten substrate 15 polymer, and the Iqminqte layer and substrate polymer are combined under a selected high pressure to form a multi-layered polymer product.

_ 2163~90 Attorney Docket No.: 1691.001 4 BR~EF DESCR~PTION OF T~E DRAWTNGS

Fig. 1 is a side view of one embodiment of the flexible reflective material of the present 5 invention.

F;g. 2 is a side view of an alternative embodiment of the flexible reflective material of the present invention.

10 Fig. 3 is a side view of an alternative embodiment of the flexible reflective material of the present invention.

Fig. 4 is a side view of an alternative embodiment of the flexible reflective material of the present invention.
lS
Fig. 5 is a side view of an alternative embodiment of the flexible reflective material of the present invention.

Figs. 6A and 6B are side views ofthe m~chine for m~mlf~cturing a multi-layered 20 polymer material of the present invention, connected by a match line.

~ 2163390 Attorney Docket No.: 1691.001 5 Fig. 7 is a top view of the portion of the m~chine for m~nuf~cturing a multi-layered polyrner material of the present invention, corresponding to that shown in Fig. 6A.

Fig. 8 is a opposite side view of a portion of the m~ ine for making the multi-layered 5 material, showing the roller gears.

~ 2163390 Attorney Docket No.: 1691.001 6 DETA~LED DESCRIPTION OF T~E JNVENTION

As used herein "a" means one or more than one. The following examples are 5 int~nded to describe various embodiments of the invention but are not intçnded to limit the scope ofthe claims. The present invention provides a flexible reflective material 10.
The material 10 is preferably substantially free from optical chatter. By "optical chatter"
- is meant transverse lines or waves of distorted reflective image app~ ;ng on the surface ofthe material 10. By "sl~b~ ly free from optical chaner" is meant that sub~ ;ally 10 no image distorting transverse lines appear in the material 10 to the unaided eye viewing the reflective material 10 securely mounted to a planar surface. This effect is achieved by the combination of ~lem~nts in the reflective material 10, the "~r.hine and the process for the manufacture of the reflective material 10, described below.

As seen in Fig. 1, the material 10 has a reflective layer 12 co~ ;ng a first acrylic layer 14, a tr~nclllcPnt polymer layer 16, and a first metal layer 18 that is disposed between the acrylic layer 14 and the tr~nclucent polymer layer 16. The material 10 also has a substrate layer 20 adjacent to the reflective layer 12. The substrate layer 20 can be a variety of polymers, but is p. efel dbly acrylic or a polyester, 20 such as, a polyethylene terephthalate (PET). In preferred emborlim~nts, the material 10 is between 15 to 60 mil thick.

- -- 216~390 Attorney Docket No.: 1691.001 7 In another embodiment shown in Fig. 2, the substrate layer 20 is disposed adjacçnt the polymer layer 16, and the material 10 further has a second acrylic layer 22 disposed between the polymer layer 16 and the substrate layer 20. In another embodiment shown in Fig. 3, the substrate layer 20 is disposed adjacent the polymer layer 16, and the material 10 further has a second metal layer 24 disposed between the polymer layer 16 and the substrate layer 20. In another p.er.,.-ed embodiment, the first metal layer 18 is adjacent the acrylic layer and the polymer layer 16, and the second metal layer 24 is adjacent the second acrylic layer 22 and the polymer layer 16.

In another preferred embodiment shown in Fig. 4, the substrate layer 20 is disposed adjacent the polymer layer 16, and the material 10 further has a second metal layer 24 disposed between the polymer layer 16 and the substrate layer 20 and a second acrylic layer 22 disposed between the second metal layer 24 and the substrate layer 20.

In another embodiment shown in Fig. 5, the material 10 further comprises a third acrylic layer 26 adjacent the substrate layer 20 opposite the reflective layer 12. In some preferred embodiments, the first metal layer 18 is adjacent the first acrylic layer 14 and the polymer layer 16. The invention cont~mplates a variety of additional layer co...binalions, not exemplified herein.

Attorney Docket No.: 1691.001 8 Referring more generally to Figs. 1-~, the first, second or third acrylic layers 14, 22, 26 can generally be an acrylic comonomer or copolymer, such as acrylic acid, methyl acrylic acid, and derivatives thereof. A description of such acrylics is, for example, in U.S. Patent No. 5,035,945, which is hereby incorporated by reference in its entirety.

The metals in the metal layers 18, 24 can be selected from ai~ln~inl-m~ silver, gold, pl~tinum, chromium, zinc, copper, nickel, p~ Ai~m, and tit~nhlrn~ and alloys thereof, for example. The deposit of such metals on a polymer layer 16 can be performed by a variety of conventional m~t~llising teçhnigues, for example, by 10 deposition from a suspension of finely divided metallic particles in a suitable liquid vehicle, or by electrode beam evaporation, electrolysis plating, or by vacuum deposition.

The tr~n~luc~nt polymer layer 16 is generally a film of polymeric material, such as polyethylene ter~hth~l~te ~PET). The composite reflective layer 12 is co,~ ..,rcially 15 available from MEI (Agawam, ~f~cs~chnsetts) as a Melinex-type product (e.g., Melinex-453). In preferred embotlim~ontc, the reflective layer 12 is between 1 to 5 mil. thick.

The material 10 also has a substrate layer 20 adhered to the reflective layer 12, which can comprise a polyester. In particular, the polyester can be a polyethylene 20 terephthalate (PET), poly ( l ,4-cyclohexylene dimethylene terephthalate) (PCT), or a combination thereof. The substrate layer 20 can also be modified by a variety of chemical processes, such as glycol modification discucced in more detail below. Jn - 216~390 Attorney Docket No.: 1691.001 9 plefelled embo-lim~nts, the substrate layer 20 is between I to 250 mil. thick. The substratê layer 20 can comprise a pigment to provide color, such as black, to the material 10. ~-ldition~l additives can also be added to the substrate 20, such as ultraviolet light stabilizers, anti-oxidants, fire lela.dan~s, acrylics, tedlar coating or 5 adhesives, etc. The invention cont~mrl~tçs that a conventional heat-activated adhesive can also be used to secure the layers 20, 12, ~Ithol~gh the emb~iments described herein do not contain such an adhesive. Another substrate malerial may be added to the substrate 20, as by means of a co-extruder 46 assembly, as described below with rël~ence to the m~hine and process for the m~nl-f~ re ofthe material 10. In one 10 embo~liment7 the substrate layer 20 is 1,4-cyclohexylene-dimethylene-e~ lene ter~ph~ te (PCT-G). PCT-G is co-----,~,.~ially available as PCTG Kodar copolyester 5445 from Eastman Chemical Company (Kingsport, Tenn~ssee). PCT-G is an amorphous (non-crystalline) thermoplastic polyester of the PCT family. The "G" in the PCT-G design~tion in~ic~t~s the use of a second glycol in making the polymer.

In a prefe. ~ ~,d embo~im~nt~ the polyester of the substrate layer 20 is ethylene-1,4-cyclohexylene-dimethylene terephthalate (PET-G). PET-G is co-,ul~ ,;ally available as PETG Kodar copolyester 6763 from ~Stm~n Chemical Comr~ny (Kingsport, Tçnnçssee). PET-G is an amorphous (noncrystalline) thermoplastic 20 polyester of the PET family. The "G" in the PET-G designation in~ic~t~s the use of a second glycol (1,4-cyclohexane~i-neth~nol, or CHDM) in making the polymer. A PET-G substrate layer 20 results in a preferred flexible reflective material 10 that is especially 163~90 Astorney Docket No.: 1691.001 10 substantially free from optical chatter and exhibits suprisingly high optical clarity.

Some of the physical properties of PET-G are generally as follows. PET-G has a tensile strength at break of about 4,000 psi (28 MPa), and a tensile strength at yield of 5 about 7,300 psi (50 MPa). The elongation at break is about 130%. The mod~ s and elasticity in bending is 2.9 x 105 psi (2,000 ~a). The flexular strength is about 10,000 psi (69 MPa). PET-G can be extrusion cast into film in thic~n~cc.os as light as about 0.025 mm (I mil) and into sheet thicLnesses greater than 6.4 mm (250 mils) on conventional extrusion eql~iprn~nt Film and 5heçting products of 0.254 mm (10 mils) or 10 more will prel;.ably be nip-polished on a three-roll stack to ensure better gauge control and improved surface appearance. PET-G must be predried, but not to the degree required for normal PET. Good heat stability permits processing te ..p~al,~res to vary as required for di~- ~nt gauges and output rates.

The flexible reflective material 10 comprising PET-G of the present invention poss~ses many unique qualities. For example, the present material 10 permits vacuum molding to about 30% deeper than similar previous products. Previous products can not be drawn deeper than 1/2" at a 45 degree angle without failure, such as split~ing of the substrate 20 or reflective layer 12. The present invention, howeva, can be drawn 20 over a rolled edge about I inch at an 80 degree angle without failure. The material 10 is heat sealable and sonic weldable, unlike prior products which crack or peel during such procedures. The PET-G substrate 20 adhesion to the reflective layer 12 is about 20%

Attorney Docket No.: 1691.001 l l higher than other products, which avoids peeling and de~ g product failures. The low melting point of PET-G (about 178~F) assists in the layer adhesion process.

The materials of the present invention are made by a - ~hine shown generally in 5 Figs. 6-8 by a process as follows. PET substrate 20 pellets should be dried before extrusion for about four to six hours at about 300~F. PET-G substrate 20 pellets should be dried before extrusion for about four to six hours at about 150~F. PCT-G substrate - 20 pellets should be dried before extrusion for about four hours at about 160~F. Acrylic substrate 20 pellets should be dried before extrusion for about six hours at about 190~F.
10 As seen in Fig. 6A, a dehllmidifying-type hopper dryer 30 should plefelably be used to produce a dewpoint of-38~F with an air flow for PET, PET-G, PCT-G and acrylic of about 1200 to 1800 cfm. Drying equipm~nt should ~rerèl ably be fitted with a dewpoint meter and an alarm. Care should be exercised in the drying-hopper design to ensure uniform pêilet and air flow, i.e., no çh~nn~ling While moisture bubblês or streaks 15 become readily visible in extruded substrate 20 if the moisture content is exc~ssively high, an un~cceFtable ievel of moisture may be present, but not obvious during extrusion. The moisture level of the pellets just before extrusion should preferably not exceed about 0.08%. Higher levels will result in a signifi~nt reduction in molecular weight, and thus, cause the substrate 20 to have considerably lower toughness that can 20 be obtained with properly dried pellets. This higher moisture level can also result in processing problems such as substrate 20 sticking to the chill roll stack 50 and die lip 44 buildup.

- ~163390 Attorney Docket No.: 1691.001 12 The primary dryer 30 preferably has a conventional desicc~nt bed (features not detailed) with a molecular sieve for water adsorption, blowers to provide airflow, heaters to vaporize the water, filters to remove dust and fines, an after-cooler to remove water from the air, and a hopper which serves as a drying container and provides a base 5 cone for uniform pellet flow. The most co-l.--lon type of d~o~icc~nt used in plastics drying is an alkali metal alumino-silicate molecular sieve with a chemic~l formula (Nal2[(AI02)12(SiO2)l2)]. Molecular sieve is generally available in powder form, in 1/16"
and 1/8" pellets, 8" x 12" and 4" x 8" beads, and 14" x 30" mesh (Union Carbide Corp., Tarrytown, NY).

Preferably, the dryer 30 is a fully automatic, self-contained adsorption type dehllmi~lifier co.~ g two molecular sieve desicc~nt beds, one supplying dPhllm;~ified air while the other is being regenerated. Such a dryer 30 is available from Universal Dynamics, Inc. (Woodbridge, Virginia) as a DHD-60. The dçh~m;~ifi~r preferably has a 15 microprocessor (Ornni II-E) for control of process air flow and temperature, which is in turn monitored and controlled by a central processing unit ("CPUn, not shown) described in more detail below. To assure moisture free substrate 20, a second dryer (not shown) also monitored and controlled by the CPU can be inc~lled intermedi~tely between the first dryer 30 and the extruder 32.

An extruder 32, shown in Figs. 6A and 7A, receives the dried substrate 20 pellets and heats the material 10 to a molten consistency. The extruder 32 is hollow Attorney Docket No.: 1691.001 13 and elone~ted, having a first substrate receiving end 34, a second substrate extruding -end 36, at least one heater element (not detailed) along the length thereof, and a screw means (not shown) for moving the substrate 20 therethrough. Such an extruder 32jS
available from Cin~inn~ti Milicrom, Inc. The extruder 32 preferably has six heater zones 5 along the length thereof in thermal comm~nication with the substrate 20, which are each monitored and controlled by the CPU. At the extruding end, the molten substrate 20 is moved through at least one screen pack 38, a pump 40, at least one adapter 42, a static mixer 43 and across the die lip 44.

As with other polymers, the substrate 20 W;ll soften and becorne tacky as it approaches its glass transition te.l.p~,.al~lre(TB). For PET-G, the T8 is 81 ~C (178~F).
For PCT-G, the TBjS 88~C (190~F). PET-G and PCT-G have better hydrolytic stability than PET and, cor-cequ~ontly, their molecular weight will not break do~hn as readily during extrusion. The nominal target inherent viscosity (I.V.) of PET~ and PCT-G
15 pellets is 0.75. When pellets are dried and extruded under the suggested conditions, the resulting I.V. should be about 0.71 to 0.73, and the extruded substrate 20 should exhibit excellent toughness If the pellets are not properly dried or are extruded at too high a te.npe.~lure, the resulting I.V. may be too low, and the substrate 20 may be somewhat brittle and contain surface distortions.

The molecular weight of a polymer is an important p, opc. ly because it is an indication ofthe toughness (or brittlen~ss) ofthe extruded substrate 20. The higher the Attorney Docket No.: 1691.001 14 molecular weight, the tougher the substrate 20. Molecular weight is very difficult to determine directly. However, inherent viscosity is a direct indication of molecular weight, and it is much easier to measure. While the measurement of I.V. is rather simple colllpal~d to dete...-i~ g molecular weight, it can be hazardous because ofthe 5 ch~m:~lc involved. A safer technique is to determine the flow rate of the substrate 20, which can then be converted to I.V. by using a correlation curve. This method is known to those skilled in the art.

A minimnm extrusion barrel length to diameter ratio (L/D) of 24/1 is suggested 10 for optimum stability and production rate. The extruder 32 drive motor (not shown) should be sized according to the output desired, and a properly de~igne~ screw (not shown) should be used. An output of approximately 3.6 to 4.5 kg/hr (8 to lO Ib/hr) per horsepower can be expected for eq~ipm~nt designed for PET-G or PCT-G. However, screws specifically designed for other polymers may yield con~id~rably less output per 1 5 horsepower.

This screw is pl~fel~bly characterized by a double-flighted section that provides a channel for llnmelted pellets as well as one for the molten substrate 20. This separation of melted and unmelted substrate 20 results in more efficient melting and 20 helps prevent overheating. For example, the output rate for a 3 1/2-in. extruder 32 with a barrier screw having an L/D ratio of 24/1 and operating at 95 rpm is greater than 318 kg (700 Ib) per hour. The drive power required under these conditions is less than 75 Attorney Docket No.: 1691.001 15 hp. Preferably, the extruder 32 drive motor has about 250 hp rotating about 4.5 in.
double-ftighted screw having a L/D ratio of 30/1.

Gauge variation in the m~hine direction of substrate 20 extruded from virgin 5 material is approximately +4%. When extruding substrate 20 it may be helpful to use internal screw cooling in the first three or four feed flights. This will help prevent pellet bridging in the hopper throat and in the screw feed section and will provide uniform feeding. Screws cooled along their entire length are not reco,~ f ~~de~ The temperature zones l eco-. --.-f nded for extruding the various substrates are dicc~ l~sed in 10 more detail below in Table I . The extruder 32 tenlpf;l al-lres, rate of screw rotation and internal pump 40 pressure are all monitored and controlled by the CPU.

'- 2163390 Attorney Docket No.: 1691.001 16 The following screen 38 pack is suggested for extrusion of substrate 20:

MESH QUANTl~IY

More pl ere. ably, the following screen 38 pack is sugeested for the extrusion of PET-G when making a reflective material sul.s~ ly free of optical chatter:
MESH QUANTITY

The melt pump 40 is a positive displ~cem~nt pump that runs at a co~ l speed.
20 There is a pressure sensor on both sides of the pump 40. The pressure between the extruder 32 and pump 40 is called the suction pressure, and the pressure between the pump 40 and the die lip 44 is called the discharge pressure. When the suction pressure '- 21~3390 Attorney Docket No.: 1691.001 17 drifts away from the preset pressure, the extruder 32 screw speed ~utoln~tir.~lly increases or decreases to bring the pressure back to the set point. When the extruder 32 supplies a con~a.ll amount of material 10 to the pump 40, the suction pressure and screw speed will remain constant. The melt pump 40 distributes an even flow of 5 substrate to the die lip 44 to insure accurate gauge without air bubbles or pits. The melt pump 40 pressure and extruder 32 screw speed are monitored and controlled by the CPU.

An even flow of substrate 20 will result in a uniform gauge in the m~chine 10 direction, typically about ~4%. Since the control system automatically co".pensates for ~h~nges in the extruder 32 output rate, changes in the size and amount of regrind substrate 20 have very little effect upon film gauge. The pump 40 can be a Luwa Model 45/45 which is capable of processing up to about 400 kg/hr (900 Ib/hr) of substrate 20.
The melt pump 40 should be capable of 20 to 35 rpms. The melt pump 40 receives 15 molten substrate at a pressure of about 800 to 1000 psi and extrudes the substrate 20 at about 1,000 to 2,500 psi, and prerel~bly at 1,500 psi. The pump 40 is ~l~fe.ably further equipped with a heating means for m~int~ining a temperature which is shown in Table I
with respect to specific substrates. All of the temperatures shown in Table I are monitored and controlled by the CPU.

- ~' 2163390 Attorney Docket No.: 1691.001 18 The static mixer 43, preferably a bow-tie model, is important to provide a consistent temperature throughout the substrate 20. A co-extruder 46 assembly (shown in Fig. 7A) can optionally be provided to feed another molten substrate into the die lip 44 extruding the molten first polymer substrate 20. For example, an acrylic can be co-S extruded into a line of polyester to form a multi-functional substrate layer 20.
Fc~çnti~lly, the co-extruder assembly 46 is a smaller scale duplic~te of the main extruder assembly 32 .

A flexible film extrusion die lip 44 having a two-piece body is suggested for 10 extruding substrate 20. For sheeting. a flexible die lip 44 with a strP~mlined restrictor bar is suggested. For film, the land length should be about 25 to 32 mm (1.0 to 1.25 in.), and for sheet, the land should be much longer, e.g., about 89 mm (3.5 in.) when making roughly 6.35 mm (250 mil) sheet. For film, a die lip 44 orifice of about 1,016 ~o 1,270 microns (40 to 50 mils) is suggested. For sheeting, the orifice should be at least 15 about 25% greater than the desired sheet th;~k neSs The face of the die lip 44 should be tapered rather than square-faced to permit a short side to chill roll air gap. The die lip 44 should have a good surface finish (two or four microinches) on all flow surfaces, have no hang-up areas or areas where flow is dead, and be free of all nicks and scratches.

Attorney Docket No.: 1691.001 19 Substrate 20 can be extruded either horizontally or vertically from the die lip 44 to the chill roll stack 50. However, the horizontal setup is pl~relled because of its ease of operation. While a three-roll stack 50 arrangement is pl ~fel I ed to produce heavy film and sheeting of high quality, a two-roll, S-wrap technique is usually employed for 5 thinner films. With such a unit, the chill rollers 52, 54, 56 diAmeters can be in the 256-to 510-mm (10- to 20-in.) range, depending upon the production rate desired.

A plefelled ... ~.hi.~e embodiment has a three chrome roller stack 50, which receives the molted bead of substrate 20 and ~cco..-p~ .ying l~min~te reflective layer 12 10 and co--l~l~Jses them into a single flexible reflective material 10 between the first (top) 52 and second (middle) rollers 54. The die lip 44 extrudes the molten substrate 20 between the top roller 52 and the middle roller 54. The top roller 52 is prefc.ably about 12 inches di~m~t~r and is ,~,~inl~ined at constant t~ .llp~.dlule, depen~lin~ upon the substrate 20 type, discnsced below. The middle roller 54 is preferably about 18 inches 15 di~meter and is ,..Ain~ined at conslallt temperature, depending upon the substrate 20 type, dicc~lssed below. The material 10 can be further passed around a third (lower) roller 56, that is pleftl~bly about 18 inches diAm~t~r and is ,,,A;nlAi.ltd at conctAnt temperature, depending upon the substrate 20 type, discllsced below. The plefe-led ratio of the sizes of the top:middle:lower rollers 52, 54, 56 is 2:3 :3 . More preferably, 20 the temperatures of the respecli~e rollers 52, 54, 56 are achieved by circulating heat e~cch~nged water therethrough, which is monitored and controlled by the CPU. The top, ~163390 Attorney Docket No.: 1691.001 20 middle and lower rollers 52, 54, 56 are respectively cooled or warmed to prevent sticking of the material 10 to the previous roller as it is passed thereover. The rollers 52, 54, 56 pl efe-~bly have a smooth chrome finish of two to four mi- l oh~ches to prevent substrate 20 and reflective layer 12 sticking thereto.
S
The low melt strength of PET-G and PCT-G make it plere.able that a short die lip 44 to chill roll stack 50 ~li5t~nce be used. An air gap that is too long produces excessive web sag and web instability between the die lip 44 and chill roll stack 50. This can cause the web to drag over the lower die lip 44 (as in the case of horizontal 10 extrusion) producing an excessive number of die lines in the extruded sh~etin~

When extruding PET-G or PCT-G, the takeoffunit should be such that it can be moved to within about 6 mm (l/4 in.) ofthe die lip 44 to ..~ ;,e the die lip 44 to chill roll stack 50 air gap. In addition, the vertical position of the chill rollers 52, 54, 56 15 should be ~djust~ble, as by the third hydraulic means 76, ~lisrl-ssed below. When extruding horizontally with the two-roll techn;qu~, the top of the second chill roll 54 should be about 6 to 12 mm (1/4 to l/2 in.) above the centerline ofthe die lip 44. When using a three-roll stack, the nip point between the top (first) 52 and middle (second) 54 chill rolls should be on or slightly below the centerline of the die lip 44.

' - 2163390 Attorney Docket No.: 1691.001 21 The top and middle rollers 52, 54 are rotated in syn~hrolu~alion, preferably at a rate of about l O to 50 fpm, dep~nding upon the substrate 20 being extruded and thickness desired. The top and middle rollers 52, 54 preferably rotate at about 20 to S0 fpm for thin PET and PET-G substrate 20 (I to 25 mil), and rotate at about 10 to 20 5 fpm for thicker PET and PET-G substrates 20 (25 to 60 mil) and all gauges of PCT-G
and acrylic substrate 20.

The means for rotating the rollers 52, 54, 56 is l~refe,ably a seven helical gear system available from Ko~ollm~nn Gear Corp. (New Jersey), shown in Fig. 8. The gears 10 preferably have a did..lel-ical pitch of about 2.25, a pressure angle of about 14.5 degrees, a helix angle of about 25.84 degrees and a circular tooth thicl~ncss of about 0.1386 to 0.1396 inches. The helical nature ofthe gears is believed to contributeto the smooth rotation ofthe rollers 52, 54, 56 and hence, to provide a reflective material 10 that is subst~nti~lly free from optical chatter.

The preferred gear system comprises: a first gear 58 affixed to a drive means (not shown) rotatable in a first direction and having circu...felenlially disposed helical gear teeth; a second gear 60 having circu---fel elllially disposed helical gear teeth rotatable in a second direction in commnnic~tion with the first gear 58 teeth; a third 20 gear 62 affixed to the first roller 52 and having circumferentially disposed helical gear teeth rotatable in the first direction in communication with the second gear 60 teeth; a - ~16~390 Attorney Docket No.: 1691.001 22 fourth gear 64 having circul.,felellLially disposed helical gear teeth rotatable in the second direction in conlm~ ic~tion with the second gear 60 teeth; a fi~h gear 66 affixed to the second roller 54 and having circull,ferenlially disposed helical gear teeth rotatable in the first direction in communication with the fourth gear 64 teeth; a sixth gear 68 5 having circunlfel e~ ally disposed helical gear teeth rotatable in the second direction in comm--n;c~tion with the fourth gear 64 teeth; and a seventh gear 70 affixed to the third roller 56 and having circu,,,~ele~ ally disposed helical gear teeth ~otalable in the first direction in comm~ tion with the sixth gear 68 teeth, thereby rotating the first, second and third rollers 52, 54, 56 in synchronization. The helical orientation of the 10 gear teeth, as opposed to standard lateral gear teeth, is believed to conllil,ule to a material 10 that is subs~ ly free of optical chatter.

The dictpnce between the top and the middle rollers 52, 54 is determined by a first pair of hydraulic positioning means 72 located on the top roller 52. The ~ict~nce 15 between the lower roller 56 and the middle roller 54 can also be determined by a second pair of hydraulic positioning means 74 located on the lower roller 56. The position of the middle roller 54 is fixed within the roll stack 50, however, the entire stack 50 can be moved vertically relative to the die lip 44 by a third pair of hydraulic positioning means 76. The location and pressure of the first, second and third pairs of hydraulic 20 positioning means 72, 74, 76 are monitored and controlled by the CPU. A linear potentiometer (not shown) monitors the distances. These hydraulic systems provide a ~163~90 Attorney Docket No.: 1691.001 23 much more consistent and controllable means for m~int~ining the rlist~nce between rollers than conventional pneum~tic means. Preferably, the first hydraulic positioning means 72 provides at least about 500 pli, more preferably at least 1000 pli and more ~lerel~bly about 1,300 pli, between ~djacent top and middle rollers 52, 54.

As seen in Fig. 6B, the m~chirle can further be equipped with a first tensioning roll 78 for providing l~min~tes, such as the reflective layer 12, to the extruded substrate 20 as it is being passed between the top 52 and middle rollers 54. A second ten~ nine roll 80 may be provided to supply a protective m~sl~in~ polymer larninate 82 to the 10 finished material 10 as it is being passed from the lower roller 56 through a pair of material 10 receiving rollers 84, 86. The first and second tensioning rolls 78, 80 are preferably controlled by pne~m~tic brakes, (not shown) preferably capable of applying a tensioning pressure between 30 and 160 psi. For a reflective layer 12 cont~inir~ an ~Inmimlm metal having a gold colored acrylic coat, the plefell~;d braking on the first 15 tensioning roll 78 is about 40 to 60 psi. For a reflective layer 12 col.lail~ing only an ~lumimlm metal, the preferred braking on the first tensioning roll 78 is about 100 to 140 psi. For m~s~ing l~min~te 82 the preferred braking on the second ten~ionine roll 80 is about 10 psi.

The material 10 is delivered along a conveyor 88 to a pair of opposed receiving rollers 84, 86 which rotate in the direction of the top and middle stack rollers, 52, 54 ' -- 2163~90 -Attorney Docket No.: 1691.001 24 respectively, to receive the material 10. The pa;r of receiving rollers 84, 86 preferably have a rubber surface for gripping the reflective material 10 and a means for adjusting the rlict~nce therebetween corresponding to the gauge ofthe reflective material 10. The material 10 is thus tensioned by setting the rate of rotation of the receiving rollers 84, 86 5 p,ef~-dbly up to 50% greater, relative to the rate ofthe rotation ofthe top 52 and middle rollers 54 (fpm). For thinner PET and P~T-G substrates 20, the receiving rollers 84, 86 are p-efe~ dbly set at about a 6 to 9% greater rate than the chrome rollers 52, ~4. For thicker PET and PET-G substrates 20 and all gauges of acrylic and PCT-G
substrate 20, the receiving rollers 84, 86 are preferably set at about a 10 to 12% greater 10 rate than the chrome rollers 52, ~4. These higher rate settings for the receiving rollers 84, 86 permit app.op.iate tensioning ofthe material 10, without indu~ng distorting strain. The actual rotation rate of the receiving rollers 84, 86 however, remains in synchroni~lion with the top and middle rollers ~2, 54.

As stated previously, the preferred setup for producing heavy material 10 [0.254 mm (10 mils) or heavier] and sheeting is the three-roll stack ~0. With this setup, nip-polishing (sometim~s called kiss-polishing or c~l~nd~ring) will yield considerably higher quality film or sheet that can be obtained with the two-roll, S-wrap technique. When lining out the equipment to make material 10, it is strongly suggested that the die lip 44 20 be adjusted to obtain uniform thickness across the die lip 44 width prior to bringing the Attorney Docket No.: 1691.001 25 polishing roll stack 50 into position. Failure to do so can result in poor quality material 10 having nonuniform strain and substantial optical surface distortion.

High pressures between the first and second rollers 52, 54 are necessO, y for 5 proper nip-polishing. Previously suggested roller pressures range from about 175 pli for heavy sheet, up to about 350 pli for lighter gauges. However, the hydraulic means 72 of the present invention provides a pressure of at least 500 pli and more ple~l~bly about 1,300 pli between the first and second rollers 52, 54, which yields a reflective material 10 sub~ ly free from optical chatter and which prevents dPI~...ir.~;on ofthe layers 10 12, 20. Due to these high pressure requirements, the rolls 52, 54 should be fabricated and hardened to about 48 to 50 Rockwell C hardness prior to chrome plating or else worm-tracking or grooving will occur.

Material 10 produced by the nip-polishing techni1ue not only has excellent 15 optical qualities, but it also possesses snap-back, which results from internal strains induced in the material 10 during the polishing operation. Snap-back is highly desirable in material 10 being produced for subseq-lPnt thermoforming because it reduces the amount of sag in the material 10 during heat-up for thermoforming and .~.;..;...;,~ s webbing. Nip-polished material 10 can be examined for strain uniformity by using 20 polarized light.

~163~90 Attorney Docket No.: 1691.001 26 The equipment used for winding material 10, such as the pair of receiving rollers 84, 86 previously mentioned, should be capable of precise tension control. Sudden changes in tension or uneven tension ate likely to produce wrinkles or optical chatter in the material 10. ~vlinimllm tension should be used when winding the material 10 to 5 reduce blocking tendenri~s Devices for removing static electricity from the material 10 sbould be positioned at strategic locations in the extrusion line to ~ nilll;~e dirt and dust pickup, electric shock, film ~linein~, and film blocking. Strategic locations would be just downstream 10 from the nip rolls, and just before windup. In Fig. 6B, a static bath station 92 familiar to those skilled in the art is shown for providing long-lasting protection against static.

Conditions similar to those given in Table 1 are suggested for extruding material 10 from substrate 20 PET and PET-G. In the majority of cases, the rolls 52, 54, 56 15 should be run at te.llpe.dlLIres just below the point at which sticking would occur.
When downr~ting is being used, the top roll 52 should usually be run at least about 15 to 18~F cooler than the middle roll 54 so that the material 10 will follow the middle roll 54 and release easily from the top roll 52. With a two-roll, S-~vrap setup, the first roll 52 should be run as hot as possible without film stic~in~ and the second roll 54 should 20 be ~djusted to obtain the desired material 10 flatness. The temperatures and parameters described herein are provided as p, ~;r~l . ed examples only, and are not int~nded to limit the scope ofthe invention. Each temperature in Table I is monitored and controlled by - ~163390 Attorney Docket No.: 1691.001 27 the CPU. The temperatures are believed to be variable by at least about + 5~F while ill~ g the operability ofthe invention.

TABLE I
SPROCESS TEMPERATU~ES (~F) 1-25 mil 40-60mil 1-25 mil 40-60mil Allgage Allgage PET-G PET-G PET PET Ac~x!ic PCT-G
ExtruderZone I 480 450 520 520 405 510 Extruder Zone 2 490 460 550 560 420 540 10 Extruder Zone 3 500 470 560 560 445 540 Extruder Zone 4 490 460 550 540 430 530 Extruder Zone 5 485 460 540 530 450 520 Extruder Zone 6 485 450 530 530 450 520 Screen Changer 485 450 530 520 450 520 15 Adapter 485 450 530 520 450 520 Melt Pump 485 450 530 520 450 520 Static Mixer 485 450 530 520 450 520 Co-Ex Block 485 450 530 520 450 520 Adapter 485 450 530 520 450 520 20 Die Zones 470 450 480 460470 420 470 Die Lip 470 460 480 460470 400 470 Top Roller 80-90 65-85 90 70-80 180 125 Middle Roller 110-130 90-120 110 100-120 200 130 Bottom Roller 145 145 145 145 220 180 Such a CPU computer monitoring and control system is available from FACTS, Inc. (2737 Front Street, Cuyahauga Falls, OH 44221). For exa~nple, a FACTS, Inc.
1500 Plus System is a versatile interactive data acquisition and control system Attorney Docket No.: 1691.001 28 specifically designed for extrusion line applications. The system has a broad range of capabilities including digital VO and analog inputs, temperature and speed loop control, and PID loops that can be mixed and m~tched or c~sc~ded together to provide complete extruder control. The system's configuration for di~rerel.~ products may be stored as 5 user defined product codes, allowing the user to change his entire system at the touch of a button to run a JilI~lelll product.

Therefore, the 1500 PLUS control system can be tailored to specific applications. This ple~lled system is composed ofthree major components: 1. Central 10 Processing Unit and I/O Panel Cabinet with Color Touch Information Display "TID"
monitor screen; 2. Parameter control Panels; and 3. Software (Base system & Specials if desired). Software can be custom written to provide the various control ranges for temperatures, rotation rates, pressures, etc. described herein.

Before extruding substrates 20, the extruder 32 and die lip 44 should be cleaned thoroughly. Any nicks or scratches on the die lip 44 flow surfaces should be polished.
In addition, the surfaces of the chill rollers 52, 54, 56 should be cleaned thorouL~hly.

Before start-up, polymer substrate 20 drying conditions should again be 20 chec~ed In addition, extruder 32 and die lip 44 temperatures should be checked to see that they are at the proper settings and that simple heat soaking has taken place.
,~.cSIlmin~e that the extruder 32 is ready to start, screw rotation should be started at 15 to ~163390 Attorney Docket No.: 1691.001 29 25 rpm with the dryer 30 hopper throat closed. The extruder 32 should be starve-fed until extrudate exits the die 44. The purpose of starve-feeding is to prevent drive overloading and stalling (especially during an initial run). Normally, an extruder 32 with no substrate 20 in the barrel will overload more quickly than one with substrate 20 left ~ S in it. On s lbseq-lçnt runs, it is not usually necçss~. y to starve-feed the extruder 32 because plastic substrate 20 remains in the barrel from the previous run.

Af'ler the extruder 32 has been started and a good web is observed coming from the die lip 44, the screw should be stopped and the die lip 44 cleaned before the web is 10 put on the chill rollers 52,54. It is eSs~nti~l that the e,.lre.-,;lies ofthe die lip 44 be clean in order to minimi7e die lines in the extruded substrate 20. The die lip 44 should be cleaned first with a brass spatula. It should then be cleaned with a light abrasive hous~hold cleaner such as that used for brass or copper pots, and then finally wiped with a clean cloth. If the lip 44 needs to be cleaned inside, a thin brass spatula can be used.
15 After the die lip 44 is thoroughly cleaned, the die lip 44 eAlle---ilies plus the orifice opening should be sprayed with a uniform, heavy coat of silicone release agent.

A~er the die lip 44 is cleaned, the chill roll stack 50 takeoff unit should be brought into the casting position as quickly as possible and the extruder 32 screw 20 restarted. If this is not done quickly, molten substrate 20 will drool from the die lip 44 and stick to the die lip 44 eAIlelniLies, requiring recle~ning To f~cilit~te threading ofthe
2~3390 Attorney Docket No.: 1691.001 30 takeoffequipment, it is desirable to have the unit pre-threaded with a leader of film or kraft paper. This will normally prevent the extrudate from rolling up on the die lip 44 as it first exits. As soon as the screw is restarted and polymer begins corning from the die lip 44, the chill roll stack 50 can be started and the pre-threaded leader will pick up the 5 hot web and carry it through the m~chine.

An alternative method ofthreading the takeoffunit which works as well as the above technique is as follows: with the chill roll stack ~0 backed away from the die lip 44 slightly, a piece of stiff cardboard (the same length as the die lip 44 and about 12 10 inches wide) is placed against the die lip 44 just under the orifice. When the melt first exits the die lip 44, it is caught on cardboard and carried onto the chill rollers 52, 54.
For a horizontal setup, this prevents melted material 10 from rOl Illhlg a bead and sticking to the die lip 44. Once the web is on the chill rollers 52, 54, a,r pins for holding the web edges and an knife can be positioned (not shown). At this point in the start-up, 15 the web should be observed for the presence of die lines. Some lines will probably be present. If they are large and excessive in number, the face of the die lip 44 should be ~Y~mined for polymer clinging to them and scrubbing against the web. If polymer is found on the die lip 44, an attempt should be made to remove it by carefully pushing it into the web with a thin spatula, and thus, allowing the web to carry it away.

As stated previously, a clean start-up is necess~ry to obtain substrate 20 with minimum die lines, particularly when the substrate 20 will not be nip-polished. If a ver~

~163390 Attorney Docket No.: 1691.001 31 dirty start-up is experienced and many die lines are observed, it is suggested that the start-up instructions described here be repeated, beginning with the die lip 44 cle~nin~
procedure.

During start-up with a two-roll, S-wrap unit, the first chill roller 52 should be run cooler than norrnal, since sticking is likely to occur on a freshly cleaned roller. After 10 to 15 min-ltec, a white substance will form on the roller 52, and this plate-out will aid the release of the film from the chill roller 52. As plate-out covers the roller 52, the t~ y~ ure of the roller 52 should then be increased. The white. plate-out should be allowed to remain on the roller 52 unless an excessive amount causes a problem. If spotty pickoffofthe plate-out occurs, the chill roller 52 temperature should be increased. This will remove the excessive plate-out from the roller surface. ARer a few minllt~S~ the roller 52 tenlpelatLJre can then be lowered to its previous setting (or slightly higher) to prevent excess buildup from reoccurring.
The edges ofthe material 10 should be l~hllllled with razor blade slitters located somewhere along the extruded web. The blades should be sharp industrial types, rigidly mounted to prevent optical chatter. The innl~lded angle of the cutting edge with the sheeting should be fairly small to prevent heavy edge buildup on the finished wound roll 20 go ~163390 Attorney Docket No.: 1691.001 32 The start-up suggestions listed above for a two-roll, S-wrap unit will also apply when starting a three-roll stack, with the exception of the portion dealing with plate-out.
As with the two-roll setup, the die lip 44 should be cleaned and the extruder 32 started as soon as possible after the roll stack S0 is brought into position. Also, the use of a S leader of film or kraft paper will facilitate threading the takeoffunit. Once the m~chine is running, the line and screw speeds should be adjusted to yield the desired gauge and production rate.

Next, gauge ~.,.iro,~ y should be chec~d and die af~ stments made to yield and 10 extrudate having minimal thickness variation across the web. Cut a piece of substrate 20 from the web which covers the entire width of the web. Measure the t~ic~n~ocs at two-inch intervals and mark the readings on the substrate 20 at each point checked. This will give a visual indication of the areas needing adjustm~nts over that portion of the substrate 20 from which the sample was taken. Determine which bolts (not shown) on 15 the die lip 44 need adjusting by laying the substrate 20 over a full scale die lip 44 bolt location pattern attached to a table near the extruder 32. By having bolt locations on the pattern and bolts on the die lip 44 itself numbered, one can quickly see exactly which bolts should be adjusted. Bolts in heavy areas should be tightened and bolts in thin areas should be loosened. This procedure should be repeated until the gauge variation across 20 the width is no greater than +5%, except possibly at the edges, which can be trimmed.
Edges should be adjusted as well as possible; if the edges are too thick, they can hold the nip roller 52, 54 apart causing additional gauge problems.

~163~90 Attorney Docket No.: 1691.001 33 Once these die lip 44 adjustments are made, the polishing roll stack S0 should be brought into position, and only minor ~djustm~nts should be needed. Bringing the polishing chill roll stack 50 into position at the beginning of start-up and prior to arljustine the die lip 44 will require more time and result in more scrap generation during 5 line-out. Furthermore, the proper lie-out procedure should also ~ e the pos~;bil;ly of producing substrate 20 with nonuniform strain caused by thick and thin areas.

As previously mentioned, a short die lip 44 to chill roll stack 50 air gap is needed - to 1-1;1-;-11i7~ sagging ofthe extrudate. If excess sag occurs and the extrudate contacts 10 the chill roll stack 50 too far ahead ofthe nip point, air can be ellllapped between the extrudate and the chill roll stack 50 and result in random unpolished areas. If the sag has been l..;.~ d with a short air gap and low melt te.,-pe-~ re, and air e~,l.a~ e~JL is still a problem, the chill roller 52, 54, 56 should be lowered relative to the die lip 44 so that the extrudate will go straight into the nip and be contacted by both polishing rollers 15 52, 54 siml~lt~neollsly. If this is not properly accomplished, the reflective material 10 will contain optical distortions.

Quality control is very important in any substrate 20 extrusion operation, çspeci~lly with the most preferred reflective material 10. There are at least three things 20 that should be checked routinely at various times during all production runs. These include gauge uniformity, strain level, and flow rate or I.V. Substrate 20 gauge should be checked in both the m~rhine (M.D.) and transverse (T.D.) directions. Both of these - ~163390 Attorney Docket No.: 1691.001 34 should be controlled to within +5% of the target thickness. The strain level is important because it has as an effect upon the manner in which the substrate 20 reacts during and after thermoforming. Too little strain results in a minimllrn of snap-back, and thus, the rate at which the substrate 20 sags will be too great. If the strain is too great, the 5 substrate 20 can shrink too much and actually pull out of the chains which carry the substrate 20 in thermoforming. Too much strain can also cause other forming problems such as localized sl,l 1 ~e of the substrate 20 during thermofc,.li~hlg that results in nonuniform gauge and/or wrinkles. In addition, substrate 20 with too much strain will not be as tough as it should be.

Probably the simplest method of determining the strain level is by checl~in~ M.D.
shrinkage. For blister paç~eing applications, the M.D. shrinkage should be about 8 to 10%. For applications in which the substrate 20 will be used in its extruded condition and not thermoformed, M.D. shrinkage should be minimi7ed and should Dot exceed 15 about 4 to 5%. It is important that strain be both minimal and uniform in the extruded product. The use of polarized light is an excellent nondestructive techn:que for qualitatively ch~c~ing extruded substrate 20 (or formed parts) for the presence and u n;ro.,.lily of strain. In fact, a simple polarized light apparatus can be monnted in line with the extruder 32 to monitor strain.

As stated earlier, the toughness of substrate 20 made from PET, PET-G, or, PCT-G is dependent upon its l.V ~as well as other factors such as strain and the ~163390 Attorney Docket No.: 1691.001 35 environment). Checking the I.V. is rather complicated and is not suggested as a quality control test. However, a relatively simple flow rate test, along with a conversion chart, will provide essenti~lly the same data as the I.V. test. Such tests are known to those skilled in the art.

When processing substrate 20 into material 10, it is suggested that long runs be made and that frequent stops and restarts be avoided. Even though interruptions in production can be tolerated without degradation becoming a problem, they should be avoided as much as possible to ..~;.l;...;~e the presence of die lines or optical chatter in 10 the finished product as well as the cost of the waste substrate 20.

Polyesters can be s~ticf~ctorily purged from the extruder 32 with either polyethylene or polypropylene. If a cleanup is to be made, the die lip 44 can be opened and cleaned while it is still hot without purging. The extruder 32 barrel, however, 15 should be purged before cleaning. This is suggested because polyester has a tendency to stick to metal and can be somewhat difficult to remove from the screw. These and other features of the invention will be appare"l to one skilled in the art.

Claims (33)

WE CLAIM:
1. A flexible reflective material substantially free from optical chatter comprising:
a. a reflective layer comprising, i. a first acrylic layer, ii. a translucent polymer layer, and iii. a first metal layer disposed between the acrylic layer and the translucent polymer layer; and b. a substrate layer adjacent to the reflective layer comprising a polyester.
2. The material of Claim 1, wherein the substrate layer is disposed adjacent the polymer layer and further comprising a second acrylic layer disposed between the polymer layer and the substrate layer.
3. The material of Claim 1, wherein the substrate layer is disposed adjacent the polymer layer and further comprising a second metal layer disposed between the polymer layer and the substrate layer.
4. The material of Claim 1, wherein the substrate layer is disposed adjacent the polymer layer and further comprising a second metal layer disposed between the polymer layer and the substrate layer and a second acrylic layer disposed between the second metal layer and the substrate layer.
5. The material of Claim 1, wherein the substrate layer material further comprises a third acrylic.
6. The material of Claim 5, wherein the third acrylic is adjacent the substrate layer opposite the reflective layer.
7. The material of Claim 1, wherein the first metal layer is adjacent the first acrylic layer and the polymer layer.
8. The material of Claim 4, wherein the first metal layer is adjacent the first acrylic layer and the polymer layer, and the second metal layer is adjacent the second acrylic layer and the polymer layer.
9. The material of Claim 1, wherein the first metal is selected from the group consisting of aluminum, silver, gold, platinum, chromium, zinc, copper, nickel, palladium, and titanium, and alloys thereof.
10. The material of Claim 3, wherein the second metal is selected from the group consisting of aluminum, silver, gold, platinum, chromium, zinc, copper, nickel, palladium, and titanium, and alloys thereof.
11. The material of Claim 4, wherein the second metal is selected from the group consisting of aluminum, silver, gold, platinum, chromium, zinc, copper, nickel, palladium, and titanium, and alloys thereof.
12. The material of Claim 1, wherein the translucent polymer layer comprises glycol modified polyethylene terephthalate.
13. The material of Claim 1, wherein the polyester is polyethylene terephthalate polyester.
14. The material of Claim 1, wherein the polyester is ethylene- 1,4-cyclohexylene-dimethylene terephthalate.
15. The material of Claim 1, wherein the first acrylic layer further comprises an ultraviolet light protectant component.
16. The material of Claim 2, wherein the second acrylic layer further comprises an ultraviolet light protectant component.
17. The material of Claim 5, wherein the third acrylic layer further comprises an ultraviolet light protectant component.
18. The material of Claim 1, wherein the substrate layer further comprises a fire retardant component.
19. The material of Claim 1, wherein the substrate layer further comprises a pigment.
20. The material of Claim 1, wherein the substrate layer is between about 5 to 75 mil. thick.
21. The material of Claim 1, wherein the reflective layer is between about 2 to 10 mil. thick.
22. The material of Claim 1, wherein the material is between about 10 to 75 mil thick.
23. A process of making a flexible multi-layered polymer material comprising:
a) heating a substrate polymer to a temperature above the melting point of the substrate polymer;
b) extruding the substrate polymer between a first and a second cylindrical roller laterally disposed in a roller stack frame, wherein the first cylindrical roller is mounted in the frame and has a first diameter, a first outer surface and is rotatable in a first direction about a first axis, and the second cylindrical roller is mounted in the frame below the first roller and has a second diameter, a second outer surface and is rotatable in a second direction about a second axis in parallel alignment with the first axis;
c) maintaining the first outer surface at a first temperature, and the second outer surface at a second temperature;
d) positioning the first outer surface at a selected distance from the second outer surface;
e) rotating the first and second rollers in synchronization;
f) supplying a laminate layer under tension to the outer surface of the first roller; and, g) combining the extruded substrate polymer with the laminate layer between the first and second rollers under pressure of at least about 500 pli between the rotating first and second rollers to form a unitary multilayered polymer material.
24. The process of Claim 23, wherein the rollers are smoothly rotated in synchronization by a helical gear system.
25. The process of Claim 23, wherein the rotating step is performed at a rate of about 10 to 50 feet per minute.
26. The process of Claim 23, wherein the combining step is achieved by positioning the rollers a selected distance apart by a hydraulic positioning means delivering at least 1000 psi.
27. The process of Claim 23, wherein the first roller is maintained at a temperature between about 80 to 90 degrees F and the second roller is maintained at a temperature between about 110 to 130 degrees F.
28. The process of Claim 23, wherein a third cylindrical roller is mounted in the frame and has a third diameter and a third outer surface and is rotatable in the first direction about a third axis in parallel alignment with the first and second axes, and further comprising maintaining the third surface at a third temperature simultaneous with maintaining the first and second outer surfaces at the first and second temperatures, and further comprising after the combining step, delivering the polymer from between the first and second rollers to between the second and third rollers.
29. The process of Claim 23, wherein the laminate is supplied by a rotatable laminate roll carrier tensioned by pneumatic brakes delivering between about 30 to 160 psi.
30. The process of Claim 23, further comprising after the combining step, withdrawing the material under tension.
31. The process of Claim 30, wherein the tension is provided by directing the material between a pair of receiving rollers rotating in restrained synchronization with the first and second rollers.
32. The process of Claim 23, wherein the substrate polymer is polyethylene terephthalate is ethylene- 1,4-cyclohexylenedimethylene terephthalate.
33. The process of Claim 23, wherein the laminate layer is a reflective polymer material.
CA002163390A 1995-11-21 1995-11-21 Flexible reflective material and process for making the same Abandoned CA2163390A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA002163390A CA2163390A1 (en) 1995-11-21 1995-11-21 Flexible reflective material and process for making the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA002163390A CA2163390A1 (en) 1995-11-21 1995-11-21 Flexible reflective material and process for making the same

Publications (1)

Publication Number Publication Date
CA2163390A1 true CA2163390A1 (en) 1997-05-22

Family

ID=4157009

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002163390A Abandoned CA2163390A1 (en) 1995-11-21 1995-11-21 Flexible reflective material and process for making the same

Country Status (1)

Country Link
CA (1) CA2163390A1 (en)

Similar Documents

Publication Publication Date Title
CN101189119B (en) Method for producing thermoplastic resin film
JP4519211B2 (en) Plastic sheet manufacturing method and apparatus
US8551372B2 (en) Process for producing an optical film
CN100520454C (en) Thermoplastic film and its production method
TWI391232B (en) Methods of producing an optical film
CN101180351B (en) Cellulose acylate film, and polarizing plate, optical compensation film and liquid crystal display using same
CN101738669B (en) Cellulose acylate film, process for producing the same, polarizing plate, retardation film, optical compensating film, antireflection film, and liquid-crystal display
US8349228B2 (en) Method of manufacturing cellulose film, manufacturing apparatus, optical film, polarizing plate and liquid crystal display
CN101312819B (en) Thermoplastic resin film and preparation method thereof
US9993954B2 (en) Surface protection film fabrication method and fabrication apparatus and surface protection film
CN1956835B (en) Cellulose acylate film and process for producing the same
CN101184600B (en) Method for producing thermoplastic film and optical compensation film for liquid crystal display panels produced by using the method
KR19990022070A (en) Amorphous transparent sheet of crystalline thermoplastic material
JP5130495B2 (en) Polypropylene-based laminated film and package using the same
US20100179263A1 (en) Optical film and process for producing the same
EP0394197B1 (en) Winding method and apparatus
US4859392A (en) Process and device for the production of plastic films
JP4650019B2 (en) Polypropylene-based laminated film and package using the same
CN1997507B (en) Thermoplastic film and its manufacturing method
CN101489757A (en) Optical film and method for production thereof
CA2163390A1 (en) Flexible reflective material and process for making the same
CZ2001441A3 (en) Optically isotropic polycarbonate films and a method for the production thereof
JP4857837B2 (en) Propylene resin retardation film production method
KR20100135745A (en) Method for producing partially thick resin sheet
CN101646546A (en) Method and apparatus for manufacturing uneven thickness resin sheet

Legal Events

Date Code Title Description
FZDE Discontinued

Effective date: 19981123