CA1228964A

CA1228964A - Chlorotrifluoroethylene polymer oriented films

Info

Publication number: CA1228964A
Application number: CA000464749A
Authority: CA
Inventors: Stanley B. Levy
Original assignee: EI Du Pont de Nemours and Co
Current assignee: EIDP Inc
Priority date: 1983-10-06
Filing date: 1984-10-04
Publication date: 1987-11-10
Also published as: JPS6096626A; JPH021654B2; EP0136922A3; DE3477010D1; EP0136922A2; EP0136922B1; AU3362884A; JPH0314620B2; JPH0236238A; US4544721A

Abstract

TITLE
CHLOROTRIFLUOROETHYLENE POLYMER ORIENTED FILMS
ABSTRACT OF THE INVENTION
A film of semi-crystalline poly(chlorotrifluoroethylene) or a semi-crystalline copolymer of chlorotrifluoroethylene which contain up to 5% comonomer units which film exhibits upon heat shrinking, no expansion in the direction perpendicular to stretching.

Description

64~

TITLE
CHLOROTRIFLUORO~THYLE~E POLYMER ORIENTED FILMS
BACKGROUND OF THE INVENTION
-This invention relates to chlorotrifluoroethylene polymer oriented films and a 5 process for their preparationO
Oriented films of chlorotrifluor~ethylene polymers are well known in the art. These polymers are melt extruded through an orifice to form a film and are then quenched and drawn. See for example 10 V.S. Patert 4,011,874. However, such films tend to expand in the direction perpendicular to the direction of stretching and, hence, are not practical for heat shrinking around substrates where tension in such perpendicular direction is required to hold the 15 film taut.
SUM.~ARY OF THE INVENTION
This invention provides an oriented film which is heat-shrinkable, i.e., the film can be shrunk, on heating, around a solid substrate. The 20 films are thus useful as outdoor protective coverings over a variety of objects, e.g., street 6igns, or over electrical wire and the like.
The oriented film is a film of semi-crystalline poly(chlorotrifluoroethylene) or of 25 a chlorotrifluoroethylene copolymer which contains up to 5% by weight of units of an ethylenically unsaturated copolymerizable organic monomer, which film, on heating, shrinks when shrinkage is measured in one direction and does not expand in a direction 30 perpendicular to that of first direction.
Further,the film's tensile modulus measured in said perpendicular direction remains çomparable to the modulus measured in the first direction, the creep resistance measured in said perpendicular direction ED ~383 35 ~2Z~

shows significant improvement, moi6ture barrier properties increase, surface electrical resistivity increases, and piezo-electric response i6 enhanced, In a preferred embodiment, toe films Dave a shrinkage of O to 2 percent in the direction perpendicular to the direction of stretching (hereinafter called "transverse" direction, and 6hrinkage of at least 12 percent in the direction of stretching (hereinafter called "longitudinal"
- 10 direction), when heated for 2 minutes at 150~C and, preferably, a transverse tensile modulus greater than 65 percent of the longitudinal tensile modulus at room temperature and at least a two-fold improvement in transverse creep resistance over that of the unstretched film.
Also provided is a process for the production of these films, as well as a process by which these films are heat set. Also provided are thermally dimensionally stable films.
DETAILED DESCRIPTION
.__ __ ____ _ The poly(chlorotrifluoroethylene) and the chlorotrifluoroethylene/comonomer polymers used in this invention are well known, as is the formation of films froln the polymers. The comonomer is an ethylenically unsaturated copolymerizable organic monomer. Representative comonomers include alpha-olefins, such as ethylene; fluorinated alpha-olefins, such as hexafluoropropylene, hexafluoroisobutylene, vinylidene fluoride, tetrafluoroethylene, fluorinated ethers such as perfluoroalkyl vinyl ethers and fur instance, perfluoropropyl Yinyl ether; perfluoroalkyl ethylenes BUCh as perfluorobutyl ethylenes; and the like.
Generally speaking, the polymer i extruded in melt form from an orifice and quenched to well 36~

below its melting point. The extrusion orifice can be such thaw the film produced is in flat sheet or tubular form. the film thickness will generally be between 0.5 and 100 mils before stretching and about 0.05 and 20 oils after stretching. If tubular film is to be stretched in accordance with the subject invention, the tube may irst be collapsed and laid flat, or be slit and opened intc flat eheet form The films that are subjected to the 1 stretching procedures described herein are substantially unstretched films. In otter words the films are "as-cast" films which have low moduli and strength. Normally, these films have moduli of bout 900 MPa in the transverse and longitudinal direction, 1 and exhibit a dimensional stability of about 2.0 percent in each direction when heated at 150DC (a negative dimensional change represents expansion).
To orient the films, the films are transported into contact with and partially around a 20 pair of rolls. The rolls are aligned parallel with each other and, to effectuate uniaxial stretching of film the peripheral drive speed of the first roll is slower than that of the second roll, the difference in peripteral drive speeds being such that the film ..
is stretched to at least 2.5 times the length of the unstretched iilm. The break point for many films covered herein is about 5 times the length of unstretched films. Of course, multiple rolls may also be used to effectuate stretching.
To prevent slippage of film on the rolls, the film is contacted with the rolls as, fur example, by the partial wrapping of the film around the rolls. Alternatively, conventional nip roll6 may be used to force film onto either or both rGlls.

The film must be heated to a temperature at least about 40C above the second order transition temperature of the polymer in order to accomplish the desired stretching. Preferably, this stretching temperature is between 85 and 130~C. The film need be at stretch temperature when it enters the stretch zone The heating can be accomplished by, e.g., heating the roll, or by housing the stretching apparatus in an oven.
To obtain the shrinkage characteristics in the film as a result of stretching, the film must be held under tension until cooled to below the 6ec~nd order transition temperature of the polymer. This may be accomplished by conventional cooling means applied between the second roll and the wind-up means or, alternatively, the second roll may act as a cooling means. As is common with stretched film, the very edges of the film are of non-uniform gauge relative to the remainder of the film. These edges, or "beads", are generally trimmed prior to packaging the wound film.
The film to be stretched must be a substantially amorphous Eilm in order to vbtain good oriented film. By "substantially amorphous" is meant that x-ray diffraction patterns of the film show diffusely scattered x-rays, in contrast to the more ordered 6harper patterns exhibited by semi-crystalline materials. After stretching, the film is semi-crystalline.
In addition, another critical aspect of the subject invention is the ratio of he width of the film to be stretched to the length of the stretch zone, the stretch zone being defined as toe length of film which is allowed Jo stretch at any given instant, i.e., the length of the film between the ~2i 39~aS

rolls as measured from the tangent of the film that contacts the roll. The result of too small a ratio, as seen below, i5 a film which, when re-heated, shrinks in the direction of stretching but expands in -the direction perpendicular to stretching. For purposes of the subject invention the ratio of film width to stretch zone length need be greater than about 3, preferably greater than about lOo Of course, i a partial wrap-around stretching apparatus is to be used, the distance between toe two rolls need only be greater than the thickness o th2 film in order for the film to pass between the rolls. If the stretch zone is greater, the film becomes fibrillar.
Another critical aspect of the subject invention is the degree of uniaxial 6tretching. Film stretched less than about 2.5 times its original length tends to expand upon heating in the direction perpendicular to stretchiny. When an attempt is made to stretch the film greater than about 5 times its unstretched length, the polymer fibrillates and ultimately breaks.
In the films of this invention, the tensile modulus in the direction perpendicular to the stretching, i.e., the transverse direction (TD), increases with stretch ratio and, upon completion of the uniaxial stretching as described above, remains greater than 65 percent of the ten ile modulus in the direction of stretching, i.e, the longitudinal direction (LD~. This reRult it surprising as it has generally bePn found that uniaxial stretching does not substantially alter the transverse tensile modulus.
Further, the films this invention exhibit transverse ~hrin~age of 0 to 2 percent, and 896~

longitudinal shrinkage of at least 12 percent, when heated for 2 minutes at 150~C.
The test for determining the amount of shrinkage in a non-heat-set film is as follows:
Six 10 cm x 2~5 cm samples are cut from the material, three along the direction of stretch and tree perpendicular to it. They are placed in an oven at 150DC for a period of two minutes with no restraint. After removal and air cooling, the samples are measured in their long dimension. The percent shrinkage is calculated for two directions, and the results averaged for each direction (a negative shrinkage represents expansion).
below the crystalline melting point of thy polymer.
The uniaxially stretched film produced in accordance with the procedure above can be heat set in any conventional manner to enhance dimensional stability. For example, the film can be run over a pair of rolls, the first heated to a heat set temperature about 10C below the crystalline melt temperature of the polymer, the second, acting as a cooling roll, having a temperature below the second order transition temperature of the polymer. The peripheral drive speeds of these rolls may be approximately equal to allow what is known in the art as stress relaxation or, alternatively, the second roll may be run at a speed slightly slower than the first to allow what is known as strain relaxation.
The time of heat setting is not critical 80 long as the film becomes dimensionally stableO
The test for determining dimensional stability of a heat-set film is as follo~ls:
Three 10 cm x 10 cm samples are cut from the material, one from the middle and one from near each edge. They are placed in an oven at the designated ~.Z~l~96~

temperature for a period of 30 minutes with no restraint. After removal and air cooling, the samples are measured in both the LD and TD; five measurements at equally spaced intervals are made in each direction, at 1, 3, 5, 7 and 9 cm. For each ample a percentage dimensional change is calculated and the results averaged in each direction. Zen so tested, the heat jet films are dimensionally stable and exhibit a transverse dimensional change of between 0 and 2~ and a longitudinal dimensional change of 0 to 4%, when heated for thirty minutes at 150C. Further, the transverse and longitudinal - moduli are increased over non-heat-set film, and the transverse modulus comes to within 75% of the longitudinal modulus. Surprisingly, the edge thickening, or "bead" effect evident after the uniaxial stretching detailed above is reduced, and in some cases eliminated, by the heat setting of the films. This bead elimination results in improved transverse gauge uniformity not generally evidenced with stretched, heat set film of the past.
The lack of transverse expansion, and in most cases positive transverse shrinkage, of the films of the subject invention allows those films to 25 be fit, e.g., around window casings, around cooking surfaces, over domed frames etc., and heat shrunk, thereby causing the film to draw taut. The high transverse tensile modulus allows the film to withstand conversion induced tresses, distortion and 30 warpage. Finally, the two dimensional creep resistance of the films of the subject invention reduces the need for structural support for these films.
In general, the films of this invention are 35 useful as carriers, electrical insulation, chemical ;~2~396~

barriers, thermal barriers, physical barriers, structural members, or as manufacturing aids in the following applicationso wire bundling; insulation for wires, membrane &witches, motor slots, flat cables, fIexible printed circuits, capacitors, strain gauges, under-ca~pet wiring, transformers, ultrahigh voltage cable, table splicing tapes, etc.: electrets; tamper resistant seals for outdoor use such as for utility - meters and otter tamper resistant weals; mica replacement; microwave lens/window (ovens/radomes);
tubing (spiral wound, laminated, sealed); gaskets;
diaphragms; heat exchangers7 chemical reactors;
linings; ducting: expansion joints, bags; sight-glass coverings; pond liners; shrinkable covers; column 15 packing, e.g. for distillation; de-mist devices;
pillows (evaporation control): flange safety covers;
6pill-control bladders; protective clothing: rupture disks; antistick/corrosion resistant surfacing or covering; pumps; windows and glazing; lighting lenses; solar colleetors (glazing/reflector/absorber); coated film base;
skylights; architectural panels; reflective film (metallized and laminated); green houses; covexs for photovoltaic cells; sewage treatment enclosures:
25 protective laminations (i.e., documents, signs, decals, labels); release films, metallizing carrier belt: cooking/heating equipment ( W, IR, electromagnetic): deicing surfaces: roll covering;
solar sails; drafting film; safety shields for light 30 and heat ources (bulbs, flame, etc.); chemical service; pressure sensitive tape vase; belting;
closures (cap liner); magnetic recording film bases;
punch tape bases; interior surfacing lprotective and decorative); yarn (slit film); trapping; packaging 5 (chemical, medical, sterilizable, etc.); roll leaf ~z~
.

carrier, enclosures (gloved containment boxes, oxygen tents, etc.); office machines (ribbon shield, etc.);
appliance printed control panel; roofing, cross-ply hoeing air barrier curtain; oven liners.
- The subject invention will be more fully understood with reference to the Examples.

An amorphous e~polymer film of chlorotrifluoroethylene and vinylidene fluoride (present in an amount of about 3.8 wt. percent), which was 18 inches (46c~) wide and 5 mils thick (0.13 mm) was stretched on a 2-roll stretch apparatus at 100C (measured in the 1st roll) at a film input speed of 10 ft/min (5cm/sec where the 6tretch zone was 20 oils (to result in a ratio of width of film to length of stretch zone of 31.8).
The film was stretched at the percents shown in Table I. Percent shrink in the Longitudinal Direction (LD) and the Transverse Direction (TD) and the modulus in the LD and TD were measured.

% % Shrink % Shrink Modulus MPa Stretch LD at 150C TD at 150C LD TD

250 2.0 0.0 965 896 100 12 -1.3 1503 1310 150 11.6 0 1655 1427 200 13.1 0 1772 1400 30250 13 O.S 1820 1427 300 13.4 ~.7 2013 1448 350 13.3 0.8 2013 1461 400 14 0.8 ~131 1~40 ~50 12.3 1~0 2206 1475 Attempt Jo wretch crystalline . '.
polychlorotrifluoroethylene polymers resulted in film6 that contained hole, tears or which were uneven in thickness.

An amorphous cop~lymer film similar to that used in Example I was stretched in a manner similar to that explained it example I, except the ratio of film width to tretch zone length was about 0.9.
Toe film was ~tre~ched at the percents shown in Table II. Percent shrink in the Longitudinal Direction OLD) and the Transverse Direction lTD) and the moduli in the LD and TD were measured. the Transverse Direction (TD) dimensional change was always an expansion. The LD and TD moduli did not increase as fast as in Example I, and the film became Jo fibrillar at ratios above 250% that the film could no be cut for Instron*~amples.
T BLE II
% Shrink Modulus (MPa) % Stretch LD ~150C) TD LD TD
0 ~2.0 0.0 965 896 19.0 -9.7 1103 1034 100 18.7 -9.7 1262 1083 25150 17.3 -7.3 1324 10~9 200 12.7 -6.8 1613 1172 250 11.5 -4.3 1875 300 11.5 -~.0 -Longer stretching, beginning about 25~ ended to fibrillate the filmO It is seen that the TD shrink values are negative which mean6 the film expanded in the TD.

An amorphous copolymer film similar to that 35 used in Example I was stretched in a manner 6imila:r *denotes trade mark ~.2~396~

to that explained in Example I, except what after stretching, an additional roll was used for in-line heat setting at 170C.
The film was stretched at the percents shown 5 in Table IIID LD and TD dimensional stabilities and LD and TD moduli were measured. The dimensional stability values were below 3% in the LD and 1% in the TD. In addition, the LD and TD moduli increased faster than in Example I, particularly the TD, which 10 tended to balance the moduli.
TABLE III
Dim. Stab.l Modulus (MPa) t Stretch LD (150-C) TDLD TD
0 -2.0 0.0965 896 15 50 0.0 1.01607 11~5 100 0.8 0.01820 1627 150 1.3 0.52041 1710 200 1.2 O.S2193 1724 250 0.2 0.52027 1744 20300 1.0 0.52255 1827 350 1.9 0.52082 1813 400 2.6 0.4~337 1813 1 Dimensional stability

Claims

CLAIMS:

1. A film of semi-crystalline poly(chlorotrifluoroethylene) or a semi-crystalline copolymer of chlorotrifluoroethylene which contains up to 5% by weight of units of an ethylenically unstaurated copolymerizable organic monomer, which film exhibits a shrinkage of 0 to 2 percent in a first direction in the plane of the film, and a shrinkage of at least 12 percent in a second direction in the same plane as the first and which is perpendicular to the first direction when heated for two minutes at about 150°C.

2. A film of semi-crystalline poly(chlorotrifluoroethylene) or a semi-crystalline copolymer of chlorotrifluoroethylene which contains up to 5% by weight of units of an ethylenically unsaturated copolymerizable organic monomer, which film exhibits transverse shrinkage of 0 to 2 percent, and longitudinal shrinkage of at least 12 percent, when heated for two minutes at about 150°C.

3. The film of Claim 1 or 2 wherein the ethylenically unsaturated copolymerizable organic monomer is vinylidene fluoride.

4. A process for uniaxially stretching a substantially unstretched film of amorphous poly(chlorotrifluoroethylene) or an amorphous copolymer of chlorotrifluoroethylene which contain up to 5% by weight of units of an ethylenically unsaturated copolymerizable organic monomer, comprising:
a) providing a pair of adjacent and parallel rolls, one roll having peripheral drive speed slower than that of the other;
b) contacting said substantially unstretched film under pressure against the slower driven roll and heating said film so that, in a stretch zone between said pair of rolls the film is at a temperature at least about 40°C above the second order transition temperature of the polymer; the pair of rolls being positioned so that the ratio of film width to stretch zone length is at least about 3, c) feeding said film from said slow roll into contact with and under pressure against the faster driven roll, the difference in peripheral drive speeds between the two rolls being such that the film is stretched between the rolls to between about 2.5 times the length of the unstretched film and the break point of the film; and then d) holding the film under tension while cooling the film to below the second order transition temperature of the polymer.

5. The process of Claim 4 wherein in step c) the film is stretched to between 2.5 to 5 times the length of the unstretched film.

6. The process of Claim 5 wherein the rolls are positioned so that the ratio of film width to stretch zone length is at least 10.

7. The process of Claim 4 wherein the ethylenically unsaturated copolymerizable organic monomer is vinylidene fluoride.

8. A dimensionally stable film of semi-crystalline poly(chlorotrifluoroethylene) or a semi-crystalline copolymer of chlorotrifluoroethylene which contains up to 5% of units of an ethylenically unsaturated copolymerizable organic monomer, which film exhibits a dimensional change in a first direction in the plane of the film of between 0 and 4%, and a dimensional change of between 0 and 2% in a second direction in the same plane and which is perpendicular to the first direction, when heated at 150°C for 30 minutes and the tensile modulus in said first direction is at least 1.5 times that of an as-cast film and the modulus in the second direction is at least 75% of that of the first direction.

9. A dimensionally stable film of semi crystalline poly(chlorotrifluoroethylene) or a semi-crystalline copolymer of chlorotrifluoroethylene which contains up to 5% vinylidene fluoride units which film exhibits a dimensional change in the transverse direction is between 0 and 2%, and a dimensional change in the longitudinal direction between 0 and 4% when heated at 150°C for 30 minutes, and the transverse tensile modulus is at least 1.5 times that of an as-cast film, and the transverse modulus is at least 75% of that of the longitudinal modulus.

10. The process of Claim 4 wherein after holding the film under tension while cooling, the film is heat set by heating it while under restraint.