The invention relates to a method for producing a plastic film, the method comprising extruding a plastic film, cooling the plastic film, mixing material into the plastic of the plastic film before the extrusion, the material causing cavitation bubbles in the plastic film to be stretched, and orientating the plastic film by stretching after the cooling.
The invention also relates to an apparatus for producing a plastic film, the apparatus comprising an extruder, a cooling device and at least one orientation device for orientating the extruded film.
Making a plastic film by extruding, cooling and then orientating it is known e.g. from U.S. Pat. Nos. 3,244,781 and 3,891,374. It is, however, difficult to make thin and, in particular, thin low-density films using these solutions.
EP publication 0,182,764 discloses a thin polypropylene film which contains wide and flat disc-like bubbles, which are about 80 micrometers in length and 50 micrometers in width. The film is produced by extruding material which has been foamed chemically or by means of gas and by orientating the extruded material biaxially thereafter. The result is a multipurpose plastic film with very versatile properties. However, the foaming degree of the plastic film is less than 50%, which is why the properties of the film are not good enough for all purposes.
U.S. Pat. No. 3,634,564 discloses orientation of a foamed film to obtain a fiberized film. The foamed film is formed by mixing a foam forming substance into the plastic material. The foam forming substance is extruded, which yields a foamed film, which is stretched. The bubbles of the film obtained are, however, rather large.
U.S. Pat. No. 4,814,124 discloses a film made of polyolefin and a filler which is stretched to obtain a gas permeable porous film. However, the foaming degree of such a film is not sufficiently good, nor are the mechanical properties of such a porous film sufficiently good for acoustic applications, for example.
Publications WO 99/51419 and WO 01/19596 disclose a method and apparatus for making a plastic film, wherein a film is extruded from plastic material by an extruder, the film is cooled and then orientated by stretching. Material is mixed into the plastic so that when the plastic film is stretched, cavitation bubbles are formed in the material particles mixed into the plastic. The foaming degree of the film is increased in such a manner that after or during the orientation, gas is arranged to act on the plastic film under high pressure so that the gas diffuses in the cavitation bubbles.
The object of the present invention is to provide a very good and thin foamed plastic film and a simple and reliable method and apparatus for making such a plastic film.
The method of the invention is characterized in that after the extrusion the plastic film is cooled slowly below the crystallization point.
The apparatus of the invention is characterized in that the apparatus comprises a control unit arranged to control the cooling device in such a manner that after the extrusion the plastic film cools slowly below the crystallization point.
The essential idea of the invention is that a film is extruded from plastic material by means of an extruder and material has been mixed into the plastic so that when the plastic is stretched cavitation bubbles are formed in the material particles mixed into the plastic. The film is orientated by stretching. After the extrusion the plastic film is cooled before the orientation. It is essential that the cooling of the plastic film is slow. The purpose of slow cooling is to increase the proportion of cavitation bubbles in the film, i.e. to provide as high a foaming degree as possible and as low a plastic film density as possible.
An advantage of the invention is that very thin films with a high foaming degree can be provided in a relatively simple manner. An advantage of the high foaming degree is that the electric and mechanical properties of the film are very good.
The invention will be described in greater detail in the accompanying drawings, in which
a and 8b schematically illustrate the effect of relaxation on the bubble form.
After the extruder 1 the plastic film 5 is cooled by a cooling device 8. The cooling device 8 may comprise e.g. a cooling roll 9, which is arranged in a cooling tank 10 containing a cooling medium, e.g. water. The plastic film 5 is arranged to be pressed against the cooling roll 9. The apparatus according to
After cooling the plastic film 5 is guided to a machine direction orientation device 12. The machine direction orientation device 12 comprises orientation rolls 13 whose velocities are adjusted so that they can be used for stretching the plastic film 5 and thus for orientation in the machine direction. If desired, the velocity of each orientation roll 13 can be adjusted separately. The machine direction orientation device 12 may also comprise heating means 14, such as radiation heaters, for heating the plastic film 5 in a manner known per se. The orientation rolls 13 can also be used for heating the plastic film 5 by supplying a heating medium, such as heated oil, to the orientation rolls 13 so that the orientation rolls 13 become warm. If desired, the temperature of each orientation roll 13 can be adjusted separately.
Suitable material, such as calcium carbonate particles, is mixed into the plastic 5a of the plastic film 5, and due to the influence of the particles the joint surfaces of the plastic molecules and the mixed material are torn during orientation, and thus cavitation bubbles are formed.
After the machine direction orientation device 12 the plastic film 5 is supplied to a cross-direction orientation device 15. In the cross-direction orientation device 15 the plastic film 5 is stretched in the cross-direction, i.e. orientation is performed in the direction substantially perpendicular to the direction of the orientation performed in the machine direction orientation device 12. Due to cross-direction stretching the bubbles can grow sideways and in the vertical direction in the cross-direction orientation device 15. The cross-direction orientation device 15 comprises two orientation wheels 16, and an orientation band 17 is arranged against both of the wheels. The orientation band 17 is an endless band which is guided by means of band guide rolls 18. The edges of the plastic film 5 are arranged between the orientation wheel 16 and the orientation band 17. Thus, the orientation band 17 presses the edges of the plastic film 5 firmly and evenly between the orientation band 17 and the orientation wheel 16 substantially along the whole travel of the cross-direction orientation device 15, in which case the film is not subjected to point-like pressure stress or tensile strain, and thus the plastic film stretches sideways without tearing. In
The cross-direction orientation device 15 can be placed in a casing 22 of its own. If desired, the casing 22 can be provided with heaters known per se, such as radiation heaters, to heat the plastic film 5.
After the cross-direction orientation device 15 the plastic film 5 is led to a relaxation unit 20. In the relaxation unit 20 the plastic film 5 is relaxed, and thus the plastic film shrinks a bit in a manner known per se. Finally, the plastic film 5 is wound on a reel 21.
Before the extrusion calcium carbonate particles have been mixed into the plastic 5a. Instead of calcium carbonate particles some other material may also be mixed into the plastic 5a, the material causing the joint surface of the plastic molecules and the material mixed into the plastic 5a to tear when the plastic film 5 is stretched so that cavitation bubbles are formed at the tearing points. Such a material is referred to as nucleating agent. Thus some oily substance, such as silicone oil or paraffin oil, can be mixed into the plastic 5a.The particles mixed into the plastic 5a may cause spot-like asymmetry e.g. in the electric field in the plastic 5a, whereas the oily substance mixed into the plastic does not substantially worsen the electric properties of the plastic. It is also possible to mix a substance having a melting point lower than the orientation temperature of the plastic 5a, such as paraffin, into the plastic 5a, in which case the substance melts when the plastic 5a is orientated. Also, a plastic with no adhesion to the plastic forming the plastic film may be used as a nucleating agent. For example, a nucleating agent such as polyester may be mixed into polypropylene PP. The plastic 5a may be made e.g. from polyamide PA, polyester or a polyolefin, such as polypropylene PP or polyethylene PE, or some other suitable plastic material.
The apparatus further comprises a control unit 23. The control unit 23 controls, for instance, the cooling temperature of the cooling device 8 and the heating devices of the machine direction orientation device 12 and of the cross-direction orientation device 15. Thus the control device 23 may be used for adjusting the cooling rate of the plastic film and the temperatures at which the plastic film is orientated.
In prior art solutions, the extruded plastic film is cooled as quickly as possible. The purpose is to make the cooling roll as cold as possible, whereby its temperature is 20° C., for example. Solutions are known, in which the temperature of the cooling roll is even below 0° C. In the present solution, the plastic film is, surprisingly, cooled very slowly after the extrusion. For instance, a polypropylene film is cooled at a relatively high temperature by using e.g. a cooling roll whose temperature is about 60° C. The purpose is to perform the cooling at a temperature lower than the melting temperature of the plastic but, simultaneously, at a temperature that is as high as possible. However, the cooling occurs at a temperature lower than the crystallization temperature. The crystallization temperature is a temperature at which there is a peak in the curve illustrating the heat energy transfer when the heat energy transferred by the molten plastic material is measured during the cooling of the plastic material. The melting temperature of polypropylene PP, for instance, is 167° C., and the crystallization temperature thereof about 90 to 120° C. The quicker the cooling, the lower the crystallization temperature is. The cooling may be performed e.g. at a temperature higher than 130° C. below the melting temperature of the plastic material. Preferably the cooling occurs at a temperature higher than 100° C. below the melting temperature of the plastic material.
It has surprisingly been noted that the proportion of cavitation bubble in the plastic film is bigger in slow cooling than in quick cooling. For instance, a plastic film whose proportion of air bubbles is over 70% may be produced, in which case the density of the plastic film is below 0,3 g/cm3. The reason for this is supposed to be the fact that during slow cooling, the crystallization of the plastic film can be slowed down, and thus large crystals are provided in the plastic film. The crystals are formed around the nucleating agent particles. Due to slow cooling, the crystal structure of the plastic material consists of large crystals. During the orientation of the plastic material, a cavitation bubble is formed relatively easily in a large crystal, which means that a large number of cavitation bubbles are produced. Thus the proportion of cavitation bubbles in the plastic material is quite high. The above-described solution thus functions particularly well when a crystalline plastic, such as polyester, polyamide PA or a polyolefin, e.g. polyethylene or polypropylene PP, is used as a material for the plastic film.
To cool down the plastic film sufficiently cooling has to last long enough. When e.g. polypropylene is cooled by a cooling device whose temperature is 60° C., one point is cooled about 6 seconds, for instance. It is reasonable to provide a sufficiently long cooling zone so that the velocity of the production line does not become too low. If the production rate of the plastic film line is, for instance, 10 m/min, the plastic film can be cooled at a distance of one metre, for example. The cooling device may be made sufficiently large, or there may be several cooling devices and cooling rolls one after another. Preferably the cooling of the plastic film lasts at least 5 seconds. Furthermore, the plastic film is preferably cooled less than 100° C. during this time. Thus the temperature of the plastic film is preferably reduced less than 30° C. in one second.
Most preferably the cooling is performed at normal air pressure. Thus the process is well manageable and the apparatus is simple.
In previously known prior art solutions, longitudinal orientation is performed at a fairly high temperature. For instance, when polypropylene is used, the orientation temperature in the longitudinal orientation is typically about 145° C. Surprisingly it has been noted that in terms of foaming degree very good results are achieved when the longitudinal orientation is implemented at a temperature lower than before. For instance, when polypropylene is used, the orientation temperature is about 137° C. Thus, when e.g. polypropylene PP is preferably used, the orientation temperature during the longitudinal orientation is lower than 25° C. below the melting temperature.
In previously known prior art solutions, the orientation temperature in cross-direction orientation is also relatively high. For example, when polypropylene is used, the orientation temperature has typically been about 155° C. Surprisingly it has been noted that the cross-direction orientation should also be performed at a lower temperature. For example, when a polypropylene film is orientated, the orientation temperature should be e.g. about 140° C. Thus, when e.g. polypropylene PP is used, the cross-direction orientation should preferably be performed at a temperature lower than 15° C. below the melting temperature.
Relaxation is performed by heating the film 5 close to the melting point by means of the first relaxation roll 20a. The film 5 shrinks in the cross direction during a free draw between the first relaxation roll 20a and the second relaxation roll 20b. In the longitudinal direction, the shrinkage is adjusted by means of the difference between the circumferential velocity w1 of the first relaxation roll 20a and the circumferential velocity w2 of the second relaxation roll 20b. The second relaxation roll 20b is used for cooling the plastic film 5. The operation of the relaxation unit 20 may be adjusted by means of the control unit 23.
The relaxation apparatus may also be a set of rolls comprising more than two, e.g. ten or even more, rolls. In this case the temperatures of the rolls are selected in such a manner that the temperature increases in the direction of the line and the velocity differences of successive rolls are reduced gradually.
a and 8b illustrate the effect of relaxation on the form of the bubbles 24.
V
1
=k·h
1
·π·R
2
and the volume of the bubble 20 of the relaxed film, respectively, is
V
2
=k·h
2·π·(0,8R)2,
wherein k is a shape constant.
Since the amount of gas or air inside the bubble 24 remains constant, the volume of the bubble 24 remains constant, i.e.
V1=V2
i.e.
k·h
1
·π·R
2
=k·h
2·π·0.64·R2,
which gives
h
1
=h
2·0,64,
which, for its part, gives
h
2=1,5625·h1.
Thus, the height of the bubble 24 increases 56% when the plastic film is relaxed 20% both in the longitudinal direction and in the cross direction. As the height of the bubbles 24 increases, the thickness of the film 5 increases correspondingly. The shape constant k may be assumed to be constant, because the shape of the bubbles 24 does not change essentially. For the sake of clarity, in respect of their width the bubbles 24 in
The plastic film 5 may be used for several different purposes in a manner known per se. At least one surface of the plastic film 5 can be provided with an electrically conductive coating, for instance, in which case the solution can be used e.g. as a microphone or loudspeaker in several acoustic applications, including sound attenuation. The plastic film 5 may also be provided with a permanent electric charge using e.g. the DC corona charge method.
The drawings and the related description are only intended to illustrate the inventive concept. The details of the invention may vary within the scope of the claims. Thus the orientation directions of the plastic film 5 and the order of orientations in different directions may vary. The simplest way to make a plastic film of the invention is to orientate the plastic film in the machine direction first and thereafter in the direction transverse to the machine direction.
Instead of or in addition to the above, the cooling device may also be implemented in such a manner that the cooling roll is dry and cooling medium circulation occurs inside it, or the cooling device may be some other cooling device solution known per se. To increase the foaming degree and reduce the density, gas may be supplied to the cavitation bubbles. Gas supply may be performed during the orientation or after it, for example. Gas supply may be performed, for example, between the longitudinal orientation and the cross-direction orientation. Furthermore, the plastic film need not necessarily be produced in a continuous production line but after the extrusion and the cooling, the plastic film preform may be stored temporarily. In this case the orientation of the plastic film by stretching does not occur until after the temporary storing. Hence, the extrusion and cooling of the plastic film may be performed in a place entirely different from that of the orientation of the plastic film. By means of temporary storing, the produced plastic film billets are provided with maximum crystallinity. The plastic film billet may also be treated thermally, i.e. heated and cooled alternately to improve the crystallinity. This thermal treatment may also be implemented in a continuous process, which is a process where the plastic film billet is not stored temporarily. Furthermore, e.g. the relaxation unit may be a separate apparatus and a treatment process, in which the already wound and orientated film may be treated in the above manner.
Number | Date | Country | Kind |
---|---|---|---|
20055500 | Sep 2005 | FI | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/FI06/50236 | 6/5/2006 | WO | 00 | 3/19/2008 |