CA2160517A1 - Molecularly oriented polymer profiles - Google Patents
Molecularly oriented polymer profilesInfo
- Publication number
- CA2160517A1 CA2160517A1 CA002160517A CA2160517A CA2160517A1 CA 2160517 A1 CA2160517 A1 CA 2160517A1 CA 002160517 A CA002160517 A CA 002160517A CA 2160517 A CA2160517 A CA 2160517A CA 2160517 A1 CA2160517 A1 CA 2160517A1
- Authority
- CA
- Canada
- Prior art keywords
- profile
- precursor
- molecular orientation
- thickness
- polymer
- 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
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 22
- 239000002243 precursor Substances 0.000 claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 claims abstract description 14
- 238000010924 continuous production Methods 0.000 claims abstract description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 29
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 29
- -1 polyethylene terephthalate Polymers 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 17
- 230000009467 reduction Effects 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 7
- 229920000573 polyethylene Polymers 0.000 claims description 7
- 239000002952 polymeric resin Substances 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229920006158 high molecular weight polymer Polymers 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- 239000000047 product Substances 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 101150010783 Aard gene Proteins 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910001094 6061 aluminium alloy Inorganic materials 0.000 description 1
- 241001514881 Metaplastes Species 0.000 description 1
- 235000018734 Sambucus australis Nutrition 0.000 description 1
- 244000180577 Sambucus australis Species 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/18—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets by squeezing between surfaces, e.g. rollers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/022—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion 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
- B29C48/07—Flat, e.g. panels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion 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
- B29C48/12—Articles with an irregular circumference when viewed in cross-section, e.g. window profiles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/30—Extrusion nozzles or dies
- B29C48/35—Extrusion nozzles or dies with rollers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/90—Thermal treatment of the stream of extruded material, e.g. cooling with calibration or sizing, i.e. combined with fixing or setting of the final dimensions of the extruded article
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C43/00—Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
- B29C43/32—Component parts, details or accessories; Auxiliary operations
- B29C43/44—Compression means for making articles of indefinite length
- B29C43/46—Rollers
- B29C2043/461—Rollers the rollers having specific surface features
- B29C2043/465—Rollers the rollers having specific surface features having one or more cavities, e.g. for forming distinct products
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/90—Thermal treatment of the stream of extruded material, e.g. cooling with calibration or sizing, i.e. combined with fixing or setting of the final dimensions of the extruded article
- B29C48/906—Thermal treatment of the stream of extruded material, e.g. cooling with calibration or sizing, i.e. combined with fixing or setting of the final dimensions of the extruded article using roller calibration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/90—Thermal treatment of the stream of extruded material, e.g. cooling with calibration or sizing, i.e. combined with fixing or setting of the final dimensions of the extruded article
- B29C48/908—Thermal treatment of the stream of extruded material, e.g. cooling with calibration or sizing, i.e. combined with fixing or setting of the final dimensions of the extruded article characterised by calibrator surface, e.g. structure or holes for lubrication, cooling or venting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/91—Heating, e.g. for cross linking
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2027/00—Use of polyvinylhalogenides or derivatives thereof as moulding material
- B29K2027/12—Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
- B29K2027/18—PTFE, i.e. polytetrafluorethene, e.g. ePTFE, i.e. expanded polytetrafluorethene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/727—Fastening elements
- B29L2031/729—Hook and loop-type fasteners
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
Abstract
A continuous process for the production of an oriented high modulus profile is provided together with the novel profiles produced thereby. A dry polymer feedstock is melted and extruded through a die to form a profile precursor having a constant crosssection and specific dimensions. Sequential passage of the profile precursor through roller dies reduces its thickness whilst imparting molecular orientation thereto. The profile is cooled under tension to freeze in the molecular orientation thereof.
Description
Field of the Invention The present invention relates to a continuous process for the manufacture of high strength, high modulus profiles from polymeric resins and to the profiles produced thereby. More specifically, the polymer products of the process of the invention have oriented molecular structures.
Background of the Invention Organic polymers typically comprise long molecular c~inS
having a backbone of linked carbon atoms. Despite the carbon -carbon chemical bond being one of the strongest in nature, the potential strength of the polymer chains is not realized because of their random orientation and entanglement, as described in "The Strength and Stiffness of Polymers", edited by A.E. Zachariades and R. S. Porter published by Marcel Dekker, 1983.
In order to obtain optimum physical strength properties, theoretically, the polymer chains need to be disentangled and oriented in parallel one to another.
The orientation of polymers may be e.ffected by several known t~chniques including gel drawing, plastic flow extrusion or solid state deformation.
The degree of molecular orientation is generally defined by the draw ratio which in the case of drawn fibres is defined as the ratio of the length obt~ine~ after stretching (ln) to that of the original length (lo)~ The tensile modulus and strength of said polymers increase almost linearly with the draw ratio ~).
~ ~ 2160517 Gel drawing has typically been utilized for the production of fibres. Whilst some fibres available, for example polyethylene, have exhibited remarkable stiffness (i.e. a modulus of about 200 gigapascals (GPa)) and tensile strength properties (4 GPa) nevertheless such products are expensive due to the complexity of the gel drawing process.
The products prepared by the lower cost solid state deformation processes have not been found to equal the strength properties that can be achieved by gel drawing methods.
The fabrication of sophisticated oriented profiles using prior art plastic extrusion processes on a commercial scale, whilst possible for polyethylene, has not proved viable for polyethylene terephthalate (PET). Oriented profiles are defined as articles having specific dimensions, typically a thickness greater than one millimetre, with constant cross-section and infinite length. Such profiles will have some degree of molecular orientation and thus a high modulus, usually of the order of several gigapascals and a higher modulus should be obt~in~hle for lower draw ratios for PET.
Although it is known to produce strapping or thin sheets of polyethylene terephthalate, which is achieved by stretching the polymer in its predeformation state, it has simply not heretofore oved possible to manufacture oriented polyethylene terephthalate profiles having specific dimensions, similar to glass fibre reinforced pultrusions. Simply stated, processing techniques for polyethylenes and polypropylenes may not be straightforwardly extrapolated to polyethylene terephthalate.
l~ ` 2160S17 Woodhams et al. in U.S. patent 5,234,652 disclose a process involving the extrusion of a high molecular weight plastic, at or about its melt temperature, and deforming the extrudate by drawing to produce an oriented extrudate. The extrudate is rapidly cooled to preserve the orientation thereby enabling the production of high strength, high modulus articles.
In U.S. patent 4,022,863 issued to Karass et al., there is described a polyethylene terephthalate strapping and a process for the preparation thereof. The process broadly consists of drying the polyester resin and extruding said resin at a temperature between 482F and 572F. The extrudate is qll~ncheA by cooling to 122F and stretched in two con-cPclltive steps at 212F.
The draw ratio in the first stretching step is about 4 to 1 whereas that in the s~on~ is about 2 - 2.5 to 1.
Further patents documenting a fragmentary section of the art include U.S. patent 4,858,139, U.S. patent 5,133,922, U.S.
patent 5,171,815 or U.S. patent 5,176,861.
SummarY of the Invention It is a primary ob;ective of the present invention to provide a continuous process for the production of an oriented, high strength, high modulus profile prepared from high molecular weight polymeric resins, particularly polyethylene terephthalate.
The objective further extends to the products produced thereby.
In accordance with the present invention, there is provided a continuous process for the production of an oriented high modulus profile having a thickness greater than one millimetre , ` 2160517 . .
produced from a high molecular weight polymer resin. The process comprises, in combination, melting and extruding dry polymer feedstock through a die having a constant cross-section. The semi-molten extrudate is then pumped through a calibrator to thereby provide a solid, deformable profile precursor having predetermined sectional and optionally angular, dimensions. The profile precursor is then sequentially passed through a predetermined number of roller dies, said dies being functional to reduce the profile precursor thickness by a factor of at least five in the case of polyethylene terephthalate whilst maint~; n i ng the temperature of the initial through to final profile in the range of about 200C. Tension is applied to said profile during cooling thereof to thereby retain the molecular orientation of the final product.
It is to be emphasized that during the process minimal stretch; ng ( or drawing) of the profile precursor and progressively formed profiles takes place. Furthermore, and most significantly, there is essentially no change in the shape of the profile or its specific dimensions other than the requisite reduction in thickness thereof.
Broadly stated, there is provided a continuous process for the production of an oriented high modulus profile from a high molecular weight polymer resin which comprises in combination:
melting and extruding dry polymer feedstock through a die of constant cross-section to thereby provide a deformable profile precursor having predetermined sectional, and optionally angular, dimènsions; sequentially passing said profile precursor through a predetermined number of roller dies to form said profile, said roller dies being functional to progressively reduce the profile precursor thickness by a predetermined factor, thereby imparting increasing molecular orientation thereto and applying sufficient tension to retain the profile dimensions and preserve the molecular orientation thereof; said reduction being effected under controlled temperature conditions; and cooling said profile under tension to thereby freeze in the final molecular orientation thereof.
In a ~conA broad aspect, the invention extends to a molecularly oriented polymer profile formed of polyethylene terephthalate having a modulus ranging from between about 8 to 15 GPa and a thickness greater than about one millimetre.
The invention extends still further to a polyethylene terphthalate product having increased molecular orientation with concomitant higher properties which are att~;ne~ by reducing the profile thickness by a factor greater than 4.5.
Description of the Drawinqs The present invention will be better understood with reference to the detailed description below and the following figure.
Figure 1 is a schematic of the process for the production of oriented profiles.
Description of the Preferred Embodiment The continuous process for the production of an oriented polymeric profile comprises in combination: melting the dry polymer resin feedstock in an extruder; forcing the semi - molten polymer through the extruder die having a predetermined configuration;
forcing the semi-molten extrudate through a calibrator to thereby produce a solid, deformable profile precursor having predetermined dimensions; sequentially introducing said profile precursor between sets of rollers to a) grab said profile and reduce said profile thickness a first time, b) passing said profile through a seco~
set of rollers which grab the thinner profile to maintain the desired tension and thus preserve orientation c) passing the profile through the requisite number of rollers to reduce the thickness by a predetermined amount and maintain orientation and d) finally cooling said profile under tension to thereby freeze in the final molecular orientation whilst the tension is maintained. The tension must be sufficient to retain the molecular orientation, but drawing is always to be avoided to prevent modification to the profile shape or dimensions. If the respective tensions are maintained, then the gap between the rollers determines the degree of molecular orientation imparted. The reduction in thickness causes an increase in length of the profile. However it has been observed that at draw ratios in excess of about four, increases in width can also occur.
The preparation of 'profiles', which are defined, as mentioned earlier, as articles having a constant cross-section, infinite length and specific dimensions will now be described. The specific dimensions are dictated by the configuration of the rollers and maint~;ne~ throughout processing by the application of controlled tension.
The profiles may be sheets, rods or angular chApPc as required. Additionally, profile sheets may, after cutting, be pressure formed into complex shapes. The applied pressure should be sufficient to maintain the molecular orientation both during and after the moulding process.
The polyethylene terephthalate (PET) feedstock is exhaustively dried: usually a period of about 6h is sufficient for virgin polymer, but at least about 24h was found necessary for recycle PET. Once dried, the polymer is maintained in the dried condition until procPCQP~ to avoid depolymerization and hence subsequent embrittlement of the formed product.
Any suitable polymer selected from PET, polypropylene or polyethylene having suitable melt properties, may be utilized. As described herein, the process finds particular application with respect to PET. Virgin PET pellets may be obtA;ne~ from numerous suppliers such as for example Du Pont or Eastman Kodak. Recycle PET is typically derived from ground up soft drink bottles and includes impurities such as glue, labels and so on. The preferred product, comprising about 98% pure PET flakes, has been physically cleaned and may have been treated chemically in a post polymerization process in an attempt to reverse any depolymerization that has taken place since manufacture.
Having reference to figure 1, there is shown at 1 a schematic of the complete process. The dried flakes or pellets are introduced through a hopper 10 into a single screw extruder 12.
~ ~, The extruder 12 is functional to deliver through a conventional extruder die 14 a thick, semi-molten polymer profile precursor.
The temperature of the extrudate leaving the die 14 would range between 265 to 270C.
A gear pump 16 is added to help force the extrudate via passage 15 through a calibrator 18 where it is air or water cooled to a temperature in the range of about 200C to thereby "set" the shape of the profile. When the PET grades currently available exit the die 14, they do so, as stated previously, in a semi-molten state, thus continlling to flow and lose shape prior to eventual solidification. Therefore, it is necessary to cool the semi-molten PET profile precursor to specific dimensions which is the function of the calibrator 18.
The calibrated profile is then passed through a heated tunnel 20 typically comprised of first and second tllnnel~ 20a and 20b respectively, to adjust its temperature prior to deformation by the first roller. The temperature of tunnel 20 is maint~ineA at approximately 200C. The heated profile is then passed through a first set of rollers 22 to impart a degree of molecular orientation thereto. The first tunnel 20 and rollers 22 are termed herein "Roller Die I".
Similarly, the precursor profile is sequentially passed through Roller Dies II, III and IV which comprise tunnels 24, 28 and 32 and rollers 26, 30 and 34 respectively to effect the reguisite thickness reduction and increase in the molecular orientation to arrive at the desired final profile. The rotational 216051~
speed of the 2nd, 3rd and 4th rollers is set to maintain the orientation and dimensions imparted by the previous roller (lst, 2nd and 3rd). Typically, the total thickness reduction for PET
profiles would be of the order of four or five times, whereas for polypropylene or polyethylene it may be as high as twenty times.
The rollers are specifically configured to deliver sufficient torque to achieve the desired profile and are provided with a means for heating thereof. The tunnels are constructed as boxes fabricated of foamed ceramic having an aperture in their bases for the introduction of hot air. The tunnels are typically maint~ine~ at temperatures between 150 to 220C.
The draw ratio of the heated profile through each of the roller dies typically ranges from about 1.5 to 2.5 for PET and most preferably is kept as high as practicable.
Forced air at ambient temperature, or about 20C is passed over the profile after it exits rollers 34 to effect cooling thereof. Alternately other means of cooling such as passage through cold water may be used A puller 36 is utilized to tension the profile thereby ensuring retention of the final dimensions and orientation thereof.
This is a prerequisite because until the temperature of the polymer drops below its glass transition temperature (approximately 75C
for PET), the molecules are able to resume some of their original configuration with concomitant loss of dimensions and orientation.
In summary, the operating conditions selected are such that the lowest possible process temperature is utilized. The , ~ 2160517 first tunnel in the Roller Die provides the entry temperature of the profile precursor into the first roller set, the rollers being functional to reduce the thickness of the profile and operating at their own preset temperatures. Subsequent rollers and the puller are also functional to maintain the tension on the profile and to retain the exit dimensions from the previous roller thereof.
An embodiment of the invention for producing oriented PET
profiles is provided in the following non-limitative example.
EXAMPLES
EXAMPLE I
The polyethylene terephthalate flakes were continuously introduced into an insulated drying hopper like that manufactured by Lutek Equipment Inc., Model CD lOOH CO~A;r Compudry having Power Miser II computer interface, return air temperature readout, CFH
monitor and after cooler operable in the 30 - 200C temperature range.
From the hopper the dried flakes were passed to an extruder having a gear pump like that manufactured by LCI
Corporation, Model LCI TRUDEX 45/28 having a discharge pressure of 10,000 psi, maximum differential pressure of 7,000 psi and output rate of 100 - 300 lbs. The operating temperatures of the extruder ranged from 260 - 280C in the barrel zone and 275C in the die zone. The temperatures of the gear pump comprised 270C in the suction section, 275C in the gear pump and 275C at discharge. The suction pressure of the gear pump was fixed at about 400 psi, its speed being 34 RPM.
The extrudate was forced through a flat extrusion die/calibrator like that manufactured by Metaplast Ltd. which had been adapted to extrude a profile of lOmm x lOOmm and included adaptors, a head flange and heater bands. The calibrator was formed of anodized 6061 aluminum having water and vacuum ports.
From the calibrator the profile precursor was passed through a heated tunnel (analogous to tunnel 20 of figure 1) to a first roller assemblage manufactured by Centre de Rec~erche Industrielle du Quebec which was modified to increase the maximum torque of the motors and thus the draw ratio. The roller assemblage comprised two sets of rollers, analogous to rollers 22 and 26 in figure 1 having a heated tunnel analogous to tunnel 24 of figure 1 therebetween. The speed of the profile was maintAi~e~ at 80 cm/min. The tunnel temperature of the first and subsequent tunnels was held at 200C.
From the first roller assemblage, the profile was passed through a heated tunnel (analogous to tunnel 28 of figure 1) to a ceco~ roller assemblage which would be like that manufactured by Metform International Ltd. The roller assemblage comprised two sets of rollers analogous to rollers 28 and 34 of figure 1 having a heated tunnel ( analogous to tunnel 32 of figure 1) therebetween.
The drive selected had a 5 HP AC rating with variable frequency controllers providing speed control. The oil heater for supplying the heated rollers was like that manufactured by Buhler CAnA~A Inc.
provided with dual zone heating and cooling, a mi~lo~locessor controlled with external sensor connection and operable in the 30 -13320C range.
After passage through a cooling forced air stream at ambient temperature of about 20C, the profile was tensioned by a puller having a maximum puller tension of 500 lbs. The maximum draw ratio obtAine~ was about 3.8.
A summary of the results in terms of maximum tension and draw ratio is given in Table I herebelow.
TABLE I
Temperature ofTemp of Tunnels MaximumMaximum Draw Tunnels 20, 24,28, 32 & X* Tension Ratio (C) (C) (lbs) 200 150 1600 3.8 200 100 2000 4.0 200 50 2200 4.2 wherein X* denotes the gap between the last roller and the puller.
The gap between rolls 26 was 1.25 mm.
The results of mechanical strength tests of flat oriented profile are given in Table II below.
TABLE II
Draw Ratio >4.6 4.66 Modulus mean 10.65 10.3 (GPa) minimum 10.00 9.4 maximum 12.00 12.3 stAnAArd deviation 0.75 1.2 Stress mean 344.4 344.5 at breakminimum 244.1 275.7 (MPa) maximum 405.9 414.1 stAn~Ard deviation 63.7 64.3 EXAMPLE II
This example describes the production of v-shaped angular profiles. The extruder and gear pump temperatures were identical to those detailed as was the remainder of the equipment with the exception that a v-shaped die/calibrator and v-configured rollers were utilized. The gear pump speed corresponA;ng to 80 cm/min was 30 RPM. The maximum tension measured on rolls 32 was approximately 2000 lbs. The maximum draw ratio achieved without fracture was 3.3. Selected samples having differing draw ratios were tested for mechAnical properties evaluations, the results being presented in Table III below.
TABLE III
Draw ratio Modulus, E StA~AArd Stress at StA~AArd mean (GPa) deviation break deviation on on E (GPa) (MPa) stress, MPa 1.18 3.35 0.1 79.5 1.80 5.0 0.4 108.1 3
Background of the Invention Organic polymers typically comprise long molecular c~inS
having a backbone of linked carbon atoms. Despite the carbon -carbon chemical bond being one of the strongest in nature, the potential strength of the polymer chains is not realized because of their random orientation and entanglement, as described in "The Strength and Stiffness of Polymers", edited by A.E. Zachariades and R. S. Porter published by Marcel Dekker, 1983.
In order to obtain optimum physical strength properties, theoretically, the polymer chains need to be disentangled and oriented in parallel one to another.
The orientation of polymers may be e.ffected by several known t~chniques including gel drawing, plastic flow extrusion or solid state deformation.
The degree of molecular orientation is generally defined by the draw ratio which in the case of drawn fibres is defined as the ratio of the length obt~ine~ after stretching (ln) to that of the original length (lo)~ The tensile modulus and strength of said polymers increase almost linearly with the draw ratio ~).
~ ~ 2160517 Gel drawing has typically been utilized for the production of fibres. Whilst some fibres available, for example polyethylene, have exhibited remarkable stiffness (i.e. a modulus of about 200 gigapascals (GPa)) and tensile strength properties (4 GPa) nevertheless such products are expensive due to the complexity of the gel drawing process.
The products prepared by the lower cost solid state deformation processes have not been found to equal the strength properties that can be achieved by gel drawing methods.
The fabrication of sophisticated oriented profiles using prior art plastic extrusion processes on a commercial scale, whilst possible for polyethylene, has not proved viable for polyethylene terephthalate (PET). Oriented profiles are defined as articles having specific dimensions, typically a thickness greater than one millimetre, with constant cross-section and infinite length. Such profiles will have some degree of molecular orientation and thus a high modulus, usually of the order of several gigapascals and a higher modulus should be obt~in~hle for lower draw ratios for PET.
Although it is known to produce strapping or thin sheets of polyethylene terephthalate, which is achieved by stretching the polymer in its predeformation state, it has simply not heretofore oved possible to manufacture oriented polyethylene terephthalate profiles having specific dimensions, similar to glass fibre reinforced pultrusions. Simply stated, processing techniques for polyethylenes and polypropylenes may not be straightforwardly extrapolated to polyethylene terephthalate.
l~ ` 2160S17 Woodhams et al. in U.S. patent 5,234,652 disclose a process involving the extrusion of a high molecular weight plastic, at or about its melt temperature, and deforming the extrudate by drawing to produce an oriented extrudate. The extrudate is rapidly cooled to preserve the orientation thereby enabling the production of high strength, high modulus articles.
In U.S. patent 4,022,863 issued to Karass et al., there is described a polyethylene terephthalate strapping and a process for the preparation thereof. The process broadly consists of drying the polyester resin and extruding said resin at a temperature between 482F and 572F. The extrudate is qll~ncheA by cooling to 122F and stretched in two con-cPclltive steps at 212F.
The draw ratio in the first stretching step is about 4 to 1 whereas that in the s~on~ is about 2 - 2.5 to 1.
Further patents documenting a fragmentary section of the art include U.S. patent 4,858,139, U.S. patent 5,133,922, U.S.
patent 5,171,815 or U.S. patent 5,176,861.
SummarY of the Invention It is a primary ob;ective of the present invention to provide a continuous process for the production of an oriented, high strength, high modulus profile prepared from high molecular weight polymeric resins, particularly polyethylene terephthalate.
The objective further extends to the products produced thereby.
In accordance with the present invention, there is provided a continuous process for the production of an oriented high modulus profile having a thickness greater than one millimetre , ` 2160517 . .
produced from a high molecular weight polymer resin. The process comprises, in combination, melting and extruding dry polymer feedstock through a die having a constant cross-section. The semi-molten extrudate is then pumped through a calibrator to thereby provide a solid, deformable profile precursor having predetermined sectional and optionally angular, dimensions. The profile precursor is then sequentially passed through a predetermined number of roller dies, said dies being functional to reduce the profile precursor thickness by a factor of at least five in the case of polyethylene terephthalate whilst maint~; n i ng the temperature of the initial through to final profile in the range of about 200C. Tension is applied to said profile during cooling thereof to thereby retain the molecular orientation of the final product.
It is to be emphasized that during the process minimal stretch; ng ( or drawing) of the profile precursor and progressively formed profiles takes place. Furthermore, and most significantly, there is essentially no change in the shape of the profile or its specific dimensions other than the requisite reduction in thickness thereof.
Broadly stated, there is provided a continuous process for the production of an oriented high modulus profile from a high molecular weight polymer resin which comprises in combination:
melting and extruding dry polymer feedstock through a die of constant cross-section to thereby provide a deformable profile precursor having predetermined sectional, and optionally angular, dimènsions; sequentially passing said profile precursor through a predetermined number of roller dies to form said profile, said roller dies being functional to progressively reduce the profile precursor thickness by a predetermined factor, thereby imparting increasing molecular orientation thereto and applying sufficient tension to retain the profile dimensions and preserve the molecular orientation thereof; said reduction being effected under controlled temperature conditions; and cooling said profile under tension to thereby freeze in the final molecular orientation thereof.
In a ~conA broad aspect, the invention extends to a molecularly oriented polymer profile formed of polyethylene terephthalate having a modulus ranging from between about 8 to 15 GPa and a thickness greater than about one millimetre.
The invention extends still further to a polyethylene terphthalate product having increased molecular orientation with concomitant higher properties which are att~;ne~ by reducing the profile thickness by a factor greater than 4.5.
Description of the Drawinqs The present invention will be better understood with reference to the detailed description below and the following figure.
Figure 1 is a schematic of the process for the production of oriented profiles.
Description of the Preferred Embodiment The continuous process for the production of an oriented polymeric profile comprises in combination: melting the dry polymer resin feedstock in an extruder; forcing the semi - molten polymer through the extruder die having a predetermined configuration;
forcing the semi-molten extrudate through a calibrator to thereby produce a solid, deformable profile precursor having predetermined dimensions; sequentially introducing said profile precursor between sets of rollers to a) grab said profile and reduce said profile thickness a first time, b) passing said profile through a seco~
set of rollers which grab the thinner profile to maintain the desired tension and thus preserve orientation c) passing the profile through the requisite number of rollers to reduce the thickness by a predetermined amount and maintain orientation and d) finally cooling said profile under tension to thereby freeze in the final molecular orientation whilst the tension is maintained. The tension must be sufficient to retain the molecular orientation, but drawing is always to be avoided to prevent modification to the profile shape or dimensions. If the respective tensions are maintained, then the gap between the rollers determines the degree of molecular orientation imparted. The reduction in thickness causes an increase in length of the profile. However it has been observed that at draw ratios in excess of about four, increases in width can also occur.
The preparation of 'profiles', which are defined, as mentioned earlier, as articles having a constant cross-section, infinite length and specific dimensions will now be described. The specific dimensions are dictated by the configuration of the rollers and maint~;ne~ throughout processing by the application of controlled tension.
The profiles may be sheets, rods or angular chApPc as required. Additionally, profile sheets may, after cutting, be pressure formed into complex shapes. The applied pressure should be sufficient to maintain the molecular orientation both during and after the moulding process.
The polyethylene terephthalate (PET) feedstock is exhaustively dried: usually a period of about 6h is sufficient for virgin polymer, but at least about 24h was found necessary for recycle PET. Once dried, the polymer is maintained in the dried condition until procPCQP~ to avoid depolymerization and hence subsequent embrittlement of the formed product.
Any suitable polymer selected from PET, polypropylene or polyethylene having suitable melt properties, may be utilized. As described herein, the process finds particular application with respect to PET. Virgin PET pellets may be obtA;ne~ from numerous suppliers such as for example Du Pont or Eastman Kodak. Recycle PET is typically derived from ground up soft drink bottles and includes impurities such as glue, labels and so on. The preferred product, comprising about 98% pure PET flakes, has been physically cleaned and may have been treated chemically in a post polymerization process in an attempt to reverse any depolymerization that has taken place since manufacture.
Having reference to figure 1, there is shown at 1 a schematic of the complete process. The dried flakes or pellets are introduced through a hopper 10 into a single screw extruder 12.
~ ~, The extruder 12 is functional to deliver through a conventional extruder die 14 a thick, semi-molten polymer profile precursor.
The temperature of the extrudate leaving the die 14 would range between 265 to 270C.
A gear pump 16 is added to help force the extrudate via passage 15 through a calibrator 18 where it is air or water cooled to a temperature in the range of about 200C to thereby "set" the shape of the profile. When the PET grades currently available exit the die 14, they do so, as stated previously, in a semi-molten state, thus continlling to flow and lose shape prior to eventual solidification. Therefore, it is necessary to cool the semi-molten PET profile precursor to specific dimensions which is the function of the calibrator 18.
The calibrated profile is then passed through a heated tunnel 20 typically comprised of first and second tllnnel~ 20a and 20b respectively, to adjust its temperature prior to deformation by the first roller. The temperature of tunnel 20 is maint~ineA at approximately 200C. The heated profile is then passed through a first set of rollers 22 to impart a degree of molecular orientation thereto. The first tunnel 20 and rollers 22 are termed herein "Roller Die I".
Similarly, the precursor profile is sequentially passed through Roller Dies II, III and IV which comprise tunnels 24, 28 and 32 and rollers 26, 30 and 34 respectively to effect the reguisite thickness reduction and increase in the molecular orientation to arrive at the desired final profile. The rotational 216051~
speed of the 2nd, 3rd and 4th rollers is set to maintain the orientation and dimensions imparted by the previous roller (lst, 2nd and 3rd). Typically, the total thickness reduction for PET
profiles would be of the order of four or five times, whereas for polypropylene or polyethylene it may be as high as twenty times.
The rollers are specifically configured to deliver sufficient torque to achieve the desired profile and are provided with a means for heating thereof. The tunnels are constructed as boxes fabricated of foamed ceramic having an aperture in their bases for the introduction of hot air. The tunnels are typically maint~ine~ at temperatures between 150 to 220C.
The draw ratio of the heated profile through each of the roller dies typically ranges from about 1.5 to 2.5 for PET and most preferably is kept as high as practicable.
Forced air at ambient temperature, or about 20C is passed over the profile after it exits rollers 34 to effect cooling thereof. Alternately other means of cooling such as passage through cold water may be used A puller 36 is utilized to tension the profile thereby ensuring retention of the final dimensions and orientation thereof.
This is a prerequisite because until the temperature of the polymer drops below its glass transition temperature (approximately 75C
for PET), the molecules are able to resume some of their original configuration with concomitant loss of dimensions and orientation.
In summary, the operating conditions selected are such that the lowest possible process temperature is utilized. The , ~ 2160517 first tunnel in the Roller Die provides the entry temperature of the profile precursor into the first roller set, the rollers being functional to reduce the thickness of the profile and operating at their own preset temperatures. Subsequent rollers and the puller are also functional to maintain the tension on the profile and to retain the exit dimensions from the previous roller thereof.
An embodiment of the invention for producing oriented PET
profiles is provided in the following non-limitative example.
EXAMPLES
EXAMPLE I
The polyethylene terephthalate flakes were continuously introduced into an insulated drying hopper like that manufactured by Lutek Equipment Inc., Model CD lOOH CO~A;r Compudry having Power Miser II computer interface, return air temperature readout, CFH
monitor and after cooler operable in the 30 - 200C temperature range.
From the hopper the dried flakes were passed to an extruder having a gear pump like that manufactured by LCI
Corporation, Model LCI TRUDEX 45/28 having a discharge pressure of 10,000 psi, maximum differential pressure of 7,000 psi and output rate of 100 - 300 lbs. The operating temperatures of the extruder ranged from 260 - 280C in the barrel zone and 275C in the die zone. The temperatures of the gear pump comprised 270C in the suction section, 275C in the gear pump and 275C at discharge. The suction pressure of the gear pump was fixed at about 400 psi, its speed being 34 RPM.
The extrudate was forced through a flat extrusion die/calibrator like that manufactured by Metaplast Ltd. which had been adapted to extrude a profile of lOmm x lOOmm and included adaptors, a head flange and heater bands. The calibrator was formed of anodized 6061 aluminum having water and vacuum ports.
From the calibrator the profile precursor was passed through a heated tunnel (analogous to tunnel 20 of figure 1) to a first roller assemblage manufactured by Centre de Rec~erche Industrielle du Quebec which was modified to increase the maximum torque of the motors and thus the draw ratio. The roller assemblage comprised two sets of rollers, analogous to rollers 22 and 26 in figure 1 having a heated tunnel analogous to tunnel 24 of figure 1 therebetween. The speed of the profile was maintAi~e~ at 80 cm/min. The tunnel temperature of the first and subsequent tunnels was held at 200C.
From the first roller assemblage, the profile was passed through a heated tunnel (analogous to tunnel 28 of figure 1) to a ceco~ roller assemblage which would be like that manufactured by Metform International Ltd. The roller assemblage comprised two sets of rollers analogous to rollers 28 and 34 of figure 1 having a heated tunnel ( analogous to tunnel 32 of figure 1) therebetween.
The drive selected had a 5 HP AC rating with variable frequency controllers providing speed control. The oil heater for supplying the heated rollers was like that manufactured by Buhler CAnA~A Inc.
provided with dual zone heating and cooling, a mi~lo~locessor controlled with external sensor connection and operable in the 30 -13320C range.
After passage through a cooling forced air stream at ambient temperature of about 20C, the profile was tensioned by a puller having a maximum puller tension of 500 lbs. The maximum draw ratio obtAine~ was about 3.8.
A summary of the results in terms of maximum tension and draw ratio is given in Table I herebelow.
TABLE I
Temperature ofTemp of Tunnels MaximumMaximum Draw Tunnels 20, 24,28, 32 & X* Tension Ratio (C) (C) (lbs) 200 150 1600 3.8 200 100 2000 4.0 200 50 2200 4.2 wherein X* denotes the gap between the last roller and the puller.
The gap between rolls 26 was 1.25 mm.
The results of mechanical strength tests of flat oriented profile are given in Table II below.
TABLE II
Draw Ratio >4.6 4.66 Modulus mean 10.65 10.3 (GPa) minimum 10.00 9.4 maximum 12.00 12.3 stAnAArd deviation 0.75 1.2 Stress mean 344.4 344.5 at breakminimum 244.1 275.7 (MPa) maximum 405.9 414.1 stAn~Ard deviation 63.7 64.3 EXAMPLE II
This example describes the production of v-shaped angular profiles. The extruder and gear pump temperatures were identical to those detailed as was the remainder of the equipment with the exception that a v-shaped die/calibrator and v-configured rollers were utilized. The gear pump speed corresponA;ng to 80 cm/min was 30 RPM. The maximum tension measured on rolls 32 was approximately 2000 lbs. The maximum draw ratio achieved without fracture was 3.3. Selected samples having differing draw ratios were tested for mechAnical properties evaluations, the results being presented in Table III below.
TABLE III
Draw ratio Modulus, E StA~AArd Stress at StA~AArd mean (GPa) deviation break deviation on on E (GPa) (MPa) stress, MPa 1.18 3.35 0.1 79.5 1.80 5.0 0.4 108.1 3
2.43 6.2 0.25 105.0 10 2.87 9.35 2.4 240.0 5
3.20 10.2 0.8 275.0 15 3.30 10.9 0.5 352.0 20 EXAMPLE III
This example demonstrates the potential for forming complex shapes from oriented sheet (namely flat profiles) by compression moulding t~chn~ques. A highly oriented sample having a draw of 4.4 was cut into 10 cm by 10 cm slabs from the profile and pressed between the platens of a press at 200C for 15, 30, and 60 seConAR at 100 tons and 60 sPconAR at 1 ton.
The tensile testing results are given in GPa in Table IV
herebelow.
TABLE IV
ConditionOriginal15s, 200C 30s, 200C60s,200C 60s,200C
100 tons 100 tons 100 tons 1 ton Modulus 11.37 10.38 10.9610.18 9.78 StAnA;~rd deviation1.33 1.06 0.95 1.16 0.44 16^
EXAMPLE IV
Experiments were performed on PET molded pieces (100 X 10 X 10 mm) to determine the maximum reduction ratio achievable without tension in a batchwise manner with a flat PET sheet. While the profile was preheated to 240C, the rolls were heated to only 200C to avoid melting during rolling. A sample was rolled under these conditions 15 consecutive times. The marhinP settings and the results obt~ineA are presented in Table V. The highest tensile modulus (11.4 GPa), was achieved after the 15th reduction corresponA ~ ng to an overall reduction ratio of 4.52. The width of the sample increased from 10 mm to 13.9 cm.
TABLE V
Conditions: Temperature of Polymer : 240C
Temperature of Rolls : 200C
Roll Speed : 200 cm/min L = Length between marks (mm) S = Sample thickness (mm) W = Sample width (mm) Lo/L = Draw ratio measured by length steP
Roll gap (mm) - 2.5 1.0 0.5 L (mm) 100 242 336 452 S (mm) 10 4.2 2.3 1.48 W (mm) 9.5* 13.9 Lo/L - 2.42 3.36 4.52 TM (GPa) - - - 11.4 TS (MPa) - - - 100 * After first roll (initially 10 mm)
This example demonstrates the potential for forming complex shapes from oriented sheet (namely flat profiles) by compression moulding t~chn~ques. A highly oriented sample having a draw of 4.4 was cut into 10 cm by 10 cm slabs from the profile and pressed between the platens of a press at 200C for 15, 30, and 60 seConAR at 100 tons and 60 sPconAR at 1 ton.
The tensile testing results are given in GPa in Table IV
herebelow.
TABLE IV
ConditionOriginal15s, 200C 30s, 200C60s,200C 60s,200C
100 tons 100 tons 100 tons 1 ton Modulus 11.37 10.38 10.9610.18 9.78 StAnA;~rd deviation1.33 1.06 0.95 1.16 0.44 16^
EXAMPLE IV
Experiments were performed on PET molded pieces (100 X 10 X 10 mm) to determine the maximum reduction ratio achievable without tension in a batchwise manner with a flat PET sheet. While the profile was preheated to 240C, the rolls were heated to only 200C to avoid melting during rolling. A sample was rolled under these conditions 15 consecutive times. The marhinP settings and the results obt~ineA are presented in Table V. The highest tensile modulus (11.4 GPa), was achieved after the 15th reduction corresponA ~ ng to an overall reduction ratio of 4.52. The width of the sample increased from 10 mm to 13.9 cm.
TABLE V
Conditions: Temperature of Polymer : 240C
Temperature of Rolls : 200C
Roll Speed : 200 cm/min L = Length between marks (mm) S = Sample thickness (mm) W = Sample width (mm) Lo/L = Draw ratio measured by length steP
Roll gap (mm) - 2.5 1.0 0.5 L (mm) 100 242 336 452 S (mm) 10 4.2 2.3 1.48 W (mm) 9.5* 13.9 Lo/L - 2.42 3.36 4.52 TM (GPa) - - - 11.4 TS (MPa) - - - 100 * After first roll (initially 10 mm)
Claims (5)
1. A continuous process for the production of an oriented high modulus profile from a high molecular weight polymer resin which comprises in combination:
melting and extruding dry polymer feedstock through a die of constant cross-section to thereby provide a solid profile precursor having predetermined sectional, and optionally angular, dimensions and having molecular orientation imparted thereto; sequentially passing said profile precursor through a predetermined number of roller dies to form said profile, said roller dies being functional to progressively reduce the profile precursor thickness by a predetermined factor, thereby imparting increasing molecular orientation thereto and applying sufficient tension to retain the profile dimensions and preserve the molecular orientation thereof; said reduction being effected under controlled temperature conditions; and cooling said profile under tension to thereby freeze in the final molecular orientation thereof.
melting and extruding dry polymer feedstock through a die of constant cross-section to thereby provide a solid profile precursor having predetermined sectional, and optionally angular, dimensions and having molecular orientation imparted thereto; sequentially passing said profile precursor through a predetermined number of roller dies to form said profile, said roller dies being functional to progressively reduce the profile precursor thickness by a predetermined factor, thereby imparting increasing molecular orientation thereto and applying sufficient tension to retain the profile dimensions and preserve the molecular orientation thereof; said reduction being effected under controlled temperature conditions; and cooling said profile under tension to thereby freeze in the final molecular orientation thereof.
2. A process as set forth in claim 1 wherein said high molecular weight polymer is selected from the group consisting of polyethylene terephthalate, polypropylene and polyethylene.
3. A process as set forth in claims 1 wherein said polymer is polyethylene terephthalate and the thickness reduction of said profile precursor is at least five.
4. A process as set forth in claim 1 wherein said roller dies comprise a heated tunnel and a set of rollers, said rollers being functional to reduce the thickness of said profile precursor whilst maintaining a predetermined tension on said profile to thereby provide a constant cross-section thereto.
5. A molecularly oriented polymer profile formed of polyethylene terephthalate having a modulus ranging from between about 8 to 20 GPa and a thickness greater than about one millimetre.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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CA002160517A CA2160517A1 (en) | 1995-10-13 | 1995-10-13 | Molecularly oriented polymer profiles |
US08/644,787 US5807516A (en) | 1995-10-13 | 1996-05-10 | Process of making molecularly oriented polymer profiles |
Applications Claiming Priority (1)
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CA002160517A CA2160517A1 (en) | 1995-10-13 | 1995-10-13 | Molecularly oriented polymer profiles |
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1995
- 1995-10-13 CA CA002160517A patent/CA2160517A1/en not_active Abandoned
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