[0001] This invention relates to an improved flash fibrillation process for converting thermoplastics
materials into fibrils, especially fibrils suitable for use in paper-making processes.
[0002] Flash fibrillation processes for thermoplastics materials are described in United
States patent specifications 3 081 519 and 3 227 784 and in British patent specifications
1 32-3 174, 1 336 915 and 1 446 034. Briefly, in a flash fibrillation process the
thermoplastics material and a liquid are charged to a first zone maintained at a temperature
sufficient to ensure that the thermoplastics material is fluid and that the liquid
is above its normal (i.e. at atmospheric pressure) boiling point and maintained at
a pressure sufficient to stop the liquid volatilising and then the charge is ejected
through an outlet into a second zon
p at considerably lower pressure where the temperature is below the freezing point
of the thermoplastics material and the temperature and pressure in the second zone
are selected to promote rapid volatilisation of the liquid with the result that the
forces accompanying the ejection and volatilisation shred and/or stretch the thermoplastics
material into fibrils while heat lost from the thermoplastics material to the volatilising
liquid accelerates the solidification of the thermoplastics material, The size of
the outlet is often pre-set to optimise the fibrillating forces which occur as the
charge is ejected.
[0003] Flash fibrillation processes (especially continuous processes) may suffer temporary
periods of instability during.which they produce random amounts of fibrils, foamed
thermoplastics material or solid thermoplastics material accompanied by pockets of
vapour.
[0004] This invention provides a flash fibrillation process (especially a continuous process)
for converting thermoplastics materials into fibrils wherein a pressurised dispersion
of thermoplastics material and liquid is ejected through an outlet governed by a pressure-responsive
valve set to respond to the pressure of the dispersion upstream of the valve such
that if the pressure falls below a predetermined level which is not below the level
required to stop the liquid volatilising, the valve at least partially closes and
if the pressure rises above the predetermined level the valve opens. The pressure-responsive
valve improves the stability of the fibrillation process leading to the production
of more uniform fibrils especially when the liquid comprises a mixture of water and
organic liquid and/or when the process is operated continuously. Possibly, variations
in the composition of the dispersion in the region of the outlet disturb the stability
of the process and such variations are aggravated by the use of a continuous process
where it is not practicable to improve the homogeneity of the dispersion by allowing
it to stand for about an hour prior to ejection or by the use of a multi-phase liquid.
[0005] The invention also provides apparatus for making thermoplastics fibrils by the above
flash fibrillation process comprising a pressure vessel having an outlet governed
by a pressure-responsive valve set to respond to pressure variations upstream of the
valve such that if the pressure falls below a predetermined value the valve at least
partially closes and if the pressure rises above the predetermined level the valve
opens.
[0006] Preferably the pressure-responsive valve is located within the outlet and comprises
a closure biassed into closing engagement with the entrance portion of the outlet.
Such a valve is opened when the pressure in the entrance portion is sufficient to
force the closure back against the bias. Conveniently, the bias is adjustable so that
the valve can be easily set to respond to a variety of predetermined levels of pressure.
The closure may be, for example, a spring-loaded ball, cone or chamfered bar which
seats into the entrance to the outlet. Balls and cones are preferred for outlets of
circular cross-section and bars for outlets which are slits. Preferably, the diameter
of the entrance and especially of the exit portion of the outlet is from 0.1 to 5.0
mm (most preferably from 0.5 to 3.0 mm) and the clearance between the entrance and
especially the exit portions of a slit die is from 0.1 to 5.0 mm (most preferably
from 0.15 to 0.5 mm).
[0007] The pressure vessel may be simply a reservoir fitted with a tap controlling the outlet
so that a pressurised dispersion can be ejected from the reservoir merely by opening
the tap. Preferably, the pressure vessel is provided with means for heating, pressurising
and mixing the components of the dispersion. Especially in a continuous process, means
may be provided for propelling the dispersion through the pressure vessel towards
the outlet. In one embodiment of the invention, monomers may be polymerised in the
liquid optionally when contained in the pressure vessel so as to provide a dispersion
of polymeric thermoplastics material in the liquid in situ,
[0008] The pressure vessel may be a screw extruder. Thermoplastics material may be melted
in the extruder and then a dispersion formed by injecting liquid into the molten thermoplastics
material. Particularly efficient dispersion is obtained if the liquid is injected
at a point where the thermoplastics material is at or just above (e.g. 10° above)
its melting temperature. This technique is useful when the liquid is to comprise both
water and an organic liquid because by injecting the water and organic liquid radially
into the extruder barrel through separate inlets on a common circumference of the
barrel it is easier to control whether the dispersion produced is an emulsion of water
in organic liquid or vice versa. The dispersion is conveniently pressurised and propelled
towards the outlet by the action of the screw and it can be conveniently heated by
means conventionally provided on screw extruders.
[0009] The thermoplastics material may be dispersed in water, an organic liquid or a mixture
of both. Preferably, the organic liquid should have a dissolving or swelling effect
on the thermoplastics material at least under the conditions used in the first zone.
Examples include hydrocarbons such as pentane, hexane, heptane or decane or chlorinated
and/or fluorinated hydrocarbons such as chlorofluoro ethanes. Optionally, the dispersion
may contain nucleating agents which promote rapid volatilisation of the liquid. Nucleating
agents should have critical temperatures well below the temperatures used in the first
zone and should be sparingly soluble in the dispersion. Nitrogen and carbon dioxide
are suitable. Other liquids and nucleating agents are disclosed in the patent specification
quoted earlier in this description.
[0010] Depending on the miscibility of the thermoplastics material and the liquid and on
the conditions of temperature and pressure used in the first zone, the dispersions
used in flash fibrillation processes may be single or multi-phase mixtures. Multi-phase
mixtures are preferred which comprise a dispersion of droplets of fluid polymer in
liquid. If the liquid has a swelling effect on the thermoplastics material, the droplets
will comprise a mixture of thermoplastics material and organic liquid. Most preferably,
the liquid comprises a mixture of water and an organic liquid which is miscible with
the thermoplastics material and the dispersion comprises at least three phases, namely
water, organic liquid and fluid droplets of thermoplastics material mixed with organic
liquid. Preferably, coditions are chosen to establish an emulsion of water and fluid
polymer droplets in organic liquid. Accordingly, the dispersion preferably comprises
a weight ratio of water to thermoplastics material of from 0.1 to 4.0 (especially
0.3 to 1.5):1 and a weight ratio of thermoplastics material to inorganic liquid of
from 0.5 to 0.005 (especially 0.35 to 0.02):x where x is the density of the organic
liquid relative to water.
[0011] However, it is also possible to use an emulsion of organic liquid and droplets of
fluid polymer in water. In this case the dispersion preferably comprises from 1 to
20% (preferably 2 to 8%) by weight of organic liquid and 5 to 75% (preferably 35 to
60%) by weight of thermoplastics material, the percentages being based on the weight
of water present. The use of large quantities of water increases the consumption of
energy.
[0012] The predetermined level of pressure to which the pressure-responsive valve is set
to respond is generally at least 0.1 MN/m
2 (preferably at least 0.5 MN/m
2) above the minimum pressure required to stop the liquid volatilising in the first
zone. For example, the valve may be set to respond to pressures of at least 2.0 and
3.3 MN/m
2 for pentane at 150°C and 190°C respectively or 1.3 and 2.0 MN/m
2 for hexane at 150°C and 190°C respectively. Conveniently, the pressure in the second
zone is atmospheric. Generally, the temperature of the first zone is at least 10°C
(preferably at least 25°C) above the boiling point of the liquid at the pressure employed
in the second zone.
[0013] The thermoplastics materials should have a molecular weight which would enable them
to be converted into fibres. The preferred thermoplastics materials are crystalline
especially crystalline aliphatic polyolefins such as low or high density polyethylene
or blends of the two or copolymers of ethylene with up to 20% hy weight of copolymerisable
monomers, for example, vinyl acetate or methyl, ethyl or butyl esters of acrylic or
methacrylic acids. The preferred polyolefin is a crystalline homopolymer of propylene
or a cooolymer of propylene with up to 20% by weight of ethylene preferably made by
injecting ethylene into the latter staoes of an otherwise propylene homopolymerisation
process.
[0014] The oolyolefin fibrils made according to this invention are especially suitable for
use in paper-making processes where they may be used alone or blended with conventional
paper pulps. For such purposes it is preferred that the polyolefins have melt flow
indices of from 0.1 to 30.0 (especially 0.5 to 5.0)q/10 minutes as neasured according
to British Standard 2782:105:Part C of 1970 using a 2.16 Kg load at 230°C in the case
of polymers containing a major amount of propylene and at 190°C in the case of ethylene
polymers and copolymers.
[0015] In orier to facilitate the use of the fihrils in paper-making processes, non-ionic,
anionic or cationi surfactants may be added to the dispersion prior to flash fibrillation.
Surfactants include polyvinyl alcohol
b and condensates of ethylene and propylene oxides. Other surfactants are disclosed
in the patent specifications quoted earlier in this description.
[0016] The thermoplastics material may also contain the usual additives found in thermoplastics
materials and paper such as stabilisers, pigments (epecially titanium dioxide) and
fillers (especially kaolin, chalk and talc).
[0017] The invention is further illustrated by the following descriptions which refer to
the drawings in which:
Figure 1 shows in section an outlet located in a portion of a pressure vessel wall;
Figure 2 shows in section an alternative outlet to that shown in Figure 1;
Figure 3 shows in end elevation the sleeve, bolts and springs of the outlet shown
in Figure 2;
Figure 4 shows in perspective on a larger scale the closure shown in Figure 2.
[0018] Figure 1 shows part of wall 1 of a pressure vesel into which is screwed a threaded
component 2. Component 2 together with externally threaded sleeve 3 defines an outlet
from the pressure vessel, the outlet consisting of entrance orifice 4, expanded portion
5 threaded towards one end and exit orifice 6. Sleeve 3 screws into expanded portion
5. Expanded portion 5 also houses a pressure-responsive valve consisting of a closure
in the form of a ball 7 which seats in entrance orifice 4 to close the outlet and
a spring 8 which biasses ball 7 into closing engagement with entrance 4 and which
reacts against sleeve 3 by screwing sleeve 3 into or out of expanded portion 5, the
bias in spring 8 can be easily adjusted.
[0019] Figure 2 shows an alternative outlet comprising slit dies 14 and 16 instead of orifices
4 and 6. Figure 2 shows a part of a wall 11 of a pressure vessel into which a threaded
component 12 is screwed. Component 12 together with sleeve 13 define an outlet consisting
of entrance slit die 14, expanded oortion 15 and exit slit die 16 which makes a press
fit in expanded chamber 15 and is held in place by bolts 23 which pass through flanged
ends 24 and engage in blind threaded bolt holes 22 formed in component 12. The positioning
of bolts 23 along the length of slit die 16 is shown in Figure 3.
[0020] Expanded portion 15 houses a pressure-responsive valve consisting of a closure in
the form of a chamfered bar 17 and three springs 18 as shown in Figure 3 which bias
bar 17 into closing engagement with entrance slit die 14 and which react against sleeve
13. Figure 4 shows the chamfered edges 20 of bar 17 which assist in seating bar 17
in slit die 14. The bias in springs 18 can be easily adjusted by turning bolts 23.
[0021] In opecation the position of the exit defining sleeve relative to one expanded portion
of the outlet is chosen of as to genecate a pre-serected biassing force to hold the
closure of the vaive in closing engagement with the entrance portion of the outlet.
A pressurised dispersion of thermoplastics material enters the entance portion of
the outlet and impinges upon the closure. As soon as the pressure of the mixture rises
above the level required to overcome the bias on the closure, the closure is forced
against the bias and tne valve opens allowing the dispersion to he ejected through
the outlet. If the biassing force has been chosen correctly, the dispersion is ejected
under the correct conditions for stable fibrillation. If the biassing force has not
been correctly chosen, it can be easily adjusted until the correct force is found.
[0022] The invention is further illlustrated by the following Examples.
EXAMPLES 1 TO 7
[0023] Various thermoplastics materials as specified in Table 1 were charged to a screw
extruder fitted with an outlet governed by a pressure-responsive valve as illustrated
in Figure 1. The dimensions of the exit orifice are specified in Table 1.
[0024] The thermoplastics material was conveyed to a ooint where it was melted. Pentane
(hexane in Example 7) and water were injected radially into the extruder barrel at
this point through separate inlets. The amounts injected are specified in Table 1.
In Example 4, polyvinyl alcohol surfactant was added to the water prior to injection.
[0025] The contents of the extruder barrel were propelled to the outlet by the action of
the screw and were heated to the temperatures specified in Table 1. The mixing action
of the screw produced an emulsion of water and droplets of molten thernoplastics material
in pentane. The droplets also contained absorbed pentane. The emulsion was pressurised
by the action of the screw and the pressure responsive valve was set to respond to
the pressures specified in Table 1. When the pressure of the emulsion reached these
pressures, the valve opened and emulsion was ejected through the outlet into a zone
of ambient temperature and pressure whereupon flash fibrillation ocurred. After a
brief initial period of hunting. the flash fibrillation process became stable and
produced highly un form fibrils. The surface area of the fibrils obtained is specified
in Table 1.
COMPARATIVE EXAMPLES A TO E
[0026] Examples 1 to 5 were repeated except that the outlet governed by the pressure-responsive
valve was replaced by an outlet consisting of an interrupted orifice of the same diameter.
In all cases it was found that fibrils were produced initially, but soon a large volume
of vapour was ejected from the orifice. The cooling effect produced by the volatilisation
of the large volume of liquid which had generated the vapour was sufficient to freeze
the thermoplastics material in the outlet and form a plug which blocked the outlet.
Pressure built up behind the plug until the plug was violently expelled from the outlet.
Foamed polymer was then produced which then gave way to the production of fibrils
again. However, the cycle repeated itself at irregular intervals.
[0027] The term "fluid" as applied to the droplets of thermoplastics material means that
the droplets are in a liquid state because they are molten, dissolved in the organic
liquid or swollen by the organic liquid. Preferably they are swollen.
