Background of the Invention
[0001] The invention relates to highly resilient polypropylene fibers which are particularly
useful in carpeting and upholstering.
[0002] In another aspect, the invention pertains to a process for producing highly resilient
polypropylene fibers.
[0003] Polypropylene is an ideal fiber to be used in carpeting and upholstering, limited
only by its poor resiliency. Resiliency is a measure of the ability of a fiber to
recover fully its original dimensions upon release of a stress which is compressing
it. With polypropylene carpet, this poor resiliency is best demonstrated by the "walking
out" of a sculptured carpet in a highly trafficked area, or by the matting which occurs
on the walked on areas of level pile carpets. Upholstery containing polypropylene
fibers will also exhibit this matting phenomenon.
[0004] Thus it is desirable to produce a polypropylene fiber having a sufficiently high
resiliency to resist "walking out" when used in sculptured carpeting, or to resist
matting when used in level pile carpeting and upholstering.
[0005] The resiliency of the fiber is determined by a compression recovery test, a non-ASTM
test that determines the percent height recovery of a compressed wad of carded fiber
in a specified time.
Summary of the Invention
[0006] It is an object of this invention to provide highly resilient polypropylene fibers
which are useful in carpeting, upholstering, other fabrics and other similar end uses.
[0007] It is a further object of this invention to provide a process for producing resilient
polypropylene fibers; and
[0008] It is yet a further object of this invention to provide fibers which can be made
into carpets and fabrics which are resistant to matting.
[0009] In accordance with this invention highly resilient fibers are made by a process comprising
the steps of:
(a) spinning the fibers;
(b) drawing the fibers;
(c) imparting a sharp edge angular or so-called two dimensional type crimp to the
fibers;
(d) heat treating the fibers to permanently set the crimp; and
(e) optionally cutting the filaments to staple, which may be done before or after
heat treating.
Brief Description of the Drawings
[0010] In the drawings, forming a part hereof:
Figure 1 shows compression recovery data for various heat treating temperatures at
a constant residence time of three minutes; and
Figure 2 shows compression recovery data for various residence times for a constant
heat treating temperature of 295°F.
Detailed Description of the Invention
[0011] The polypropylene which is used in the present invention may be any essentially linear
highly crystalline isotactic polypropylene which has a high molecular weight. Generally
such polymers have a melting point of about 165°C (329°F). Such polymers are commercially
available. Although any method can be used in the manufacture, the polypropylene used
in the present invention is generally prepared using a coordination polymerization
method. This polymerization method uses a reduced transition metal catalyst, generally
in the form of a slurry of a very small solid particle in an inert medium. This method
is well known in the art.
[0012] Various additives including such dye receptors as polyamines, polyvinyl pyridines,
polyamides, organic pigments such as phthalocyanine etc., inorganic pigments such
as cadmium salt series, carbon black etc., and stabilizers, plasticizers, flame retardants,
etc., may be incorporated into the polypropylene to modify the properties thereof.
[0013] The conversion of the bulk polypropylene to fiber form is accomplished by any of
the usual spinning methods. Since polypropylene can be melted under reasonable temperature
conditions, the production of the fibers is preferably done by melt spinning as opposed
to solution processes. The fibers are melt spun at a temperature in the range of about
420°F to about 640°F, with a temperature in the range of about 450°F to about 625°F
preferred.
[0014] In the process of melt spinning, the polymer is heated in an extruder to the melting
point and the molten polymer is pumped at a constant rate under high pressure through
a spinnerette containing a number of holes. The liquid polymer streams emerge downward,
or in other directions, from the face of the spinnerette usually into a cooling stream
of gas, generally air. The streams of molten polymer are solidified as a result of
cooling to form filaments and are brought together and are wound up on bobbins. If
desirable, the polymer melt in the extruder may be protected from oxygen by blanketing
it with steam or an inert gas such as carbon dioxide, nitrogen etc.
[0015] The size of the filaments will be in the range of about 1 denier/filament to about
130 denier/filament, with a filament size in the range of about 1.8 denier/filament
to about 18 denier/filament preferred.
[0016] After the fiber has been prepared, a drawing step is performed to orient the molecular
structure of the fibers. The drawing step may be carried out in any convenient manner
using techniques well known in the art such as the use of heated rolls, heated circulating
gas oven, steam oven, radiant panel heater, a heated plate, heated liquids, or the
like. The methods are not critical but the temperature should be sufficient to impart
crystallinity during drawing. Although any draw ratio (i.e., drawn length/undrawn
length) can be employed, a draw ratio above about 3.0:1 is used, preferably 3.5:1
to 6:1.
[0017] The spinning and drawing steps are done in a manner to produce sufficient crystallinity
so that the fibers can withstand the heat treating step. This requires avoiding excessive
heat in spinning for a given polymer and providing sufficient heat in drawing.
[0018] The drawn fiber can have any tenacity, but will generally have a tenacity measured
on single fibers in the range of about 3 grams/denier to about 4.5 grams/denier, with
a tenacity in the range of about 3.5 grams/denier to about 4.4 grams/denier being
preferred.
[0019] The fibers are then crimped. The type of crimp imparted to the fibers can be described
as either a sharp edge angular or non-helical crimp. These are the so-called two-
dimensional or sawtooth crimps. The preferred method of imparting such a crimp is
a stuffer box assembly.
[0020] The fiber has an average crimp count in the range of about 4 crimps per inch to about
20 crimps per inch, with an average crimp count in the range of about 6 crimps per
inch to about 15 crimps per inch being preferred, 6 to 10 being most preferred.
[0021] After a crimp is imposed in the fibers, they are taken from the texturing region
and are heated in suitable means at a temperature sufficient and for a time sufficient
to allow the crimp imparted in the fiber to be permanently set so that the fibers
will have an improved compression recovery.
[0022] Generally the fiber is heat treated at a temperature sufficient and for a residence
time sufficient to allow the crimp imparted during the crimping step to be permanently
set into the fiber so that the fiber will have a compression recovery of at least
about 250 percent, although a compression recovery of at least about 275 percent is
preferred, and a compression recovery of at least 290 percent being most preferred.
[0023] The compression recovery of the fiber after the heat treating step will of course
depend upon both the temperature at which it was treated, and the residence time for
which the fiber was treated.
[0024] Generally the heat treating temperature will be in the range of about 280°F to just
below the softening point of the fibers. The softening point of the fibers is in the
range of about 320°F to about 329°F. A preferred heat treating temperature is in the
range of about 284°F to about 315°F, with the most preferred temperature being in
the range of about 289°F to 311°F.
[0025] The residence time required to heat treat the fibers depends upon the type of heating
device used and the openness of the fiber bundle. With good heat transfer such as
with condensing steam or high velocity air, 5 seconds to 1 minute is sufficient, whereas
with lower velocity air circulation where fiber is piddled on a conveyer belt, between
1 and 8 minutes could be required. Generally, about 5 seconds to about 8 minutes,
preferably 5 seconds to 3 minutes is used, most preferably 5 seconds to 1 minute.
Once the fiber reaches the desired temperature, it takes very little time, less than
30 seconds, to obtain the desired resilience properties.
[0026] The steps of spinning, drawing, crimping and heat setting can be done as one continuous
process if desired, or spinning can be done separately and the remaining steps done
continuously, i.e. the steps can be intermittent or continuous or any combination
thereof.
[0027] The following is a description of the method used to determine compression recovery
of staple fibers.
1. Card the sample to thoroughly blend and open it.
2. Weigh three 1 gram samples to the nearest 0.1 gram.
3. Place a single 1 gram sample in a one-inch diameter cavity mold, compress to 10,000
psi, and hold for one minute.
4. Remove the sample from the mold and allow it to recover for 24 hours (if desired,
other times or multiple times can be used). Herein, unless noted, 24 hours is used.
5. Rest the one inch diameter, 5.5-gram foot of a displacement gauge on the top of
the sample. This gauge, Federal Model C81S, is mounted on Custom Scientific apparatus
Model CS 55 128.
6. Measure the height of the sample after 30 more seconds - this is height B.
7. The height of the sample immediately after one minute's compression at 10,000 psi,
height A, is difficult to measure accurately each time. To minimize such measurement
error, a standard initial height has been measured as accurately as possible, and
this height, 0.167 inches, is used for all samples.
8. Make 3 determinations per sample, and report the average of the three.
9. Calculation. Percent Compression Recovery =

x 100
[0028] Figure 1 shows the relationship between compression recovery as measured after both
24 hours and 60 seconds versus oven heat treating temperatures, at a constant residence
time of 3 minutes. This figure clearly shows the sharp increase in the fiber resilience,
as measured by compression recovery at heat treating temperatures above about 280°F.
[0029] Figure 2 shows the relationship between compression recovery as measured after 24
hours and after 60 seconds versus residence time, at a constant oven heat treating
temperature of 295°F. This figure clearly shows the sharp increase in the fiber resilience,
as measured by compression recovery at residence times above about 30 seconds.
Example
[0030] This example is provided to assist one skilled in the art to a further understanding
of the invention, without limiting the scope of the invention. Particular reactants,
components, ratios, conditions employed, are intended to be exemplary and not limitative
of the reasonable scope of the invention herein described, of which these examples
are a part of my overall disclosure.
[0031] The fibers of this example were extruded from crystalline polypropylene pellets of
eight melt index (Marlex® 9374 polypropylene made by Phillips Petroleum Co.) containing
heat and U.V. stabilizers and antioxidants and a combination of organic and inorganic
pigments to produce colored fibers. This resin was melted and brought to 520°F in
a conventional extruder, forced under pressure through spinnerettes with 70 round
holes, each hole 0.7 mm diameter, cooled with cross-flow quench air at 60°F, 90 feet
per minute, and wound onto a tube at 510 meters per minute. Lubricant and antistat
were applied during spinning.
[0032] Fiber was withdrawn from an array of these tubes to form a tow which, after drawing
at 4.8 draw ratio, was one million denier, and each drawn filament was 18 denier.
Conventional seven-roll draw stands were used, with rolls of the first and second
stands heated to 250°F and the third stand not heated. The stand speeds were 31, 125,
and 150 meters per minute. Additional fiber finish was applied after drawing. The
tow was heated with steam before entering a conventional Fleissner stuffer-box crimper
having 5-inch wide water-cooled rolls, where 6 to 8 crimps per inch were imparted.
[0033] In a separate step, the crimped tow was piddled (distributed) onto a moving perforated-metal
conveyor belt through which heated air circulated in a Proctor and Schwartz oven.
The air temperatures and residence times were those indicated in FIGURES 1 and 2.
The heat treated tow was cut to make staple of about 3.25 inches with a conventional
Lummus cutter.
[0034] While this invention has been described in detail for the purpose of illustration,
it is not to be construed or limited thereby, but is intended to cover all changes
and modifications within the spirit and scope thereof.
1. A highly resilient fiber comprising a plurality of polypropylene filaments, said
fiber characterized by:
a non-helical crimp having an average crimp count in the range of about 4 to about
20 crimps per inch preferably about 6 to about 10 crimps per inch;
a compression recovery of at least 250% preferably at least 275 %, more preferably
at least 290%.
2. A fiber as in claim 1 wherein said fiber has a tenacity in the range of about 3.5
grams/denier to about 4.4 grams/denier.
3. A method of making a highly resilient polypropylene fiber comprising the steps
of:
(a) spinning the fibers;
(b) drawing the fibers;
(c) imparting a non-helical crimp to the product of step (b),
(d) heat setting the product of step (c) at a tempera ture sufficient and a residence
time sufficient to allow the crimp imparted during step (c) to be permanently set
into the fibers so that the fibers have a compression recovery of at least 250 %,
preferably at least 275 %, more preferably at least 290 %.
4. A method as in claim 3 wherein the temperature at which the product from step (c)
is heat set is in the range of about 280°F to just below the softening point of the
fibers, and the residence time is 5 seconds to 3 minutes.
5. A method of making a highly resilient polypropylene fiber comprising the steps
of:
(a) spinning the fibers,
(b) drawing the fibers,
(c) imparting a non-helical sawtooth crimp to the product of step (b); and
(d) heat setting the product from step (c) at a temperature in the range of about
280°F to just below the softening point of the fiber for a residence time of 5 seconds
to 8 minutes.
6. Process according to claim 3, 4 or 5 wherein one of the following sets of conditions
is used:
(a) the temperature at which the product from step (c) is heat set is in the range
of about 284°F to about 315°F, and the residence time is about 5 seconds to 3 minutes.
(b) the temperature at which the product from step (c) is heat set is in the range
of about 289°F to about 311°F, and the residence time is about 5 seconds to 3 minutes.
7. A method as in one of claims 3 to 6 wherein after said step (d), said fiber is
cut into staple.
8. A method as in one of claims 3 to 6 wherein before said step (d), said fiber is
cut into staple.
9. A method as in one of claims 3 to 8 wherein said heat setting is brought about
by contact with steam, preferably the temperature being in the range of about 289°
to about 311°F and said residence time being within the range of 5 seconds to 1 minute.
10. A method according to one of the claims 3 to 8 wherein said heat setting is brought
about by high velocitiy circulation of hot air through the fibers, said residence
time is 5 seconds to 1 minute and the resulting temperature is in the range of about
289°F to 311°F.
11. Fiber produced in accordance with a method defined in one of the method claims.
12. Fabric made of fibers according to one of the claims 1, 2 or 11.