Field of The Invention
[0001] This invention generally relates to a process of treating individual fibers to have
an improved resiliency, and more particularly, to treating individual fibers with
a finish solution containing a durable press resin and a lubricant so that the fibers
have improved resiliency and other properties suitable as a fiber fill material and
for other uses.
Background Art
[0002] It is well known in fabric art to treat fabric made of cellulose fibers with urea-formaldehyde
resins and other additives, including organopolysiloxanes, to provide wrinkle-resistant
(durable press) properties. In particular, U.S. Patent 4,170,581 of Griffin, 3,177,093
of van Loo, and 2,758,946 of Spalding together are typical of the prior art teaching
durable press fabric treatments using formaldehyde-based glyoxyl resin as a crosslinking
agent to give durable press properties, and organopolysiloxanes as a soil release
or water repellant agent. To overcome the problem of release of free formaldehyde
by durable press treated fabrics, U.S. Patent 4,269,603 of Worth teaches the use of
a formaldehyde-free finishing agent containing glyoxyl with reactive silicone and
a catalyst. Alternatively, U.S. Patent 4,345,063 of North teaches durable press treatment
using alkylated condensate resin products of the reaction of glyoxyl and cyclic ureas
which are free of formaldehyde.
[0003] In home furnishing products, it is desirable to use fiber fill materials which have
good resiliency and can regain their original volume despite repeated use. Polyester
fibers are normally used because of their resiliency. Although cotton fibers would
be preferred as a fill material because of their lower cost and comfortableness of
feel, they do not have the resiliency of polyester fibers, and tend to become clumpy
or matted and do not retain their original volume after repeated use. Thus, cotton
and other natural fibers have heretofore not been suitable as a fiber fill material
for the home furnishing market. Moreover, for absorbent layers and laminates of various
types, it is desirable to use fibers which can retain their original volume during
use.
Summary of The Invention
[0004] It is therefore principal object of the invention to provide a process for treating
individual fibers to have an improved resiliency. In particular, the invention seeks
to provide a treatment for cellulosic fibers, such as cotton fibers, to have improved
properties suitable for a fiber fill material. A further object is to provide an improved
fiber product of individual fibers which are finish-treated to have an improved resiliency
and can maintain their volume.
[0005] In accordance with the invention, a process for treating individual fibers to have
an improved resiliency comprises the steps of saturating the individual fibers with
a solution containing a durable press resin and a lubricant such that the resin saturates
to the interior of the fibers while the lubricant is retained at or near the surface
of the fibers, and drying and curing the resin to be cross-linked to the fibers before
the lubricant can be absorbed into the interior of the fibers. The lubricant is selected
to have a larger molecular structure than the resin, so that the resin is absorbed
more readily into the interior of the fibers than the lubricant.
[0006] In a preferred method of the invention, scoured and bleached cotton fibers are saturated
with a solution containing a formaldehyde-free, alkylated glyoxyl/cyclic urea condensate
resin and an amino-group silicone, then dried and cured. The resultant fibers have
a resiliency equal to or better than polyester fiber. The resin component gives the
treated fibers resiliency, while the silicone imparts lubrication to the fibers to
reduce interfiber friction to allow them to slip easily across each other.
[0007] As another aspect of the invention, an improved fiber product comprises individual
fibers, and particularly individual cotton fibers, provided with a finish of a durable
press resin and a lubricant, wherein the resin is saturated and cured and cross-linked
to the interior of the fibers while the lubricant is retained at or near the surface
of the fibers. The finish-treated cotton fibers have a resiliency of about 4.1 - 5.8
centimeters or more of recovery after initial compression compared to about 4.1 centimeters
for polyester fibers, as measured by a compression-regain method of testing resiliency.
[0008] Other objects, features, and advantages of the present invention will become apparent
from the following detailed description of the best mode of practising the invention
when considered with reference to the drawings, as follows:
Brief Description of The Drawings
[0009]
Fig. 1A is a schematic diagram of a continuous process for treating individual fibers
with a resiliency-improving finish in accordance with the invention;
Fig. 1B is a schematic diagram of a batch process for treating individual fibers with
a resiliency-improving finish;
Fig. 2 is a cross-sectional diagram of a finish-treated cotton fiber in accordance
with the invention;
Fig. 3 is a schematic diagram illustrating a method of testing the resiliency of the
finish-treated fibers; and
Fig. 4 is a chart comparing the resiliency of finish-treated cotton fibers to untreated
cotton fibers and polyester fibers.
Detailed Description of Preferred Embodiments
[0010] Referring to Figs. 1A and 1B, two alternative processes for making the high resiliency
fibers in accordance with the invention are shown generally comprising the steps of
scouring and bleaching raw and unfinished fibers, saturating them with a finish solution
containing a durable press resin and a lubricant, then drying and curing the fibers
to produce the high resiliency fiber product (sometimes referred to herein as "hi-loft"
fibers). In the following description, the particular example of standard mature cotton
fibers is used, although the invention can also be applied to other cellulosic fibers,
such as cotton linters, as well as to other fibers which have, or are treated to have,
a structure which can absorb and cross-link with durable press resin.
[0011] In the continuous process option of Fig. 1A, bales of griege cotton fibers are opened
and cleaned with step cleaners. A carded mat of cotton fibers is formed. The mat is
saturated in a caustic and surfactant solution in the scouring step, and passed through
a scour steamer at a suitable temperature and time required for removal of basic impurities
such as wax, oils, pectins, etc. The mat is saturated in a bleaching solution, such
as hydrogen peroxide or sodium hypochlorite, to bleach the fibers white, passed through
a bleach steamer at a suitable temperature and time required for bleaching to occur,
and rinsed to remove the bleach liquor and adjust the pH of the fiber surface residues.
[0012] The scoured and bleached cotton fibers are then immersed in a finish bath containing
the durable press resin, the lubricant, and a catalyst. The fibers are immersed such
that the resin can saturate to the interior of the fibers while the lubricant remains
at or near the surface of the fibers. The finish-treated fibers are then dried and
cured within a time period before the lubricant can be absorbed into the interior
of the fibers. The dried mat is then broken up in a tufter and baled as the hi-loft
cotton fiber product.
[0013] The continuous process depends on the use of conveyors and other aids to transport
the carded mat of fibers through the process. The mat is preferably in the range of
24 oz./sq.yd. The heavier weight helps maintain the integrity of the fibers through
the continuous process. One advantage of this process is the locking of the fibers
in an open web state before scouring and bleaching, in order to prevent the formation
of ropes, strings, and neps associated with cotton fibers processed in batches.
[0014] In the kier process option of Fig. 1B, bales of griege cotton fibers are opened and
cleaned with step cleaners. The fibers are then saturated with a caustic and surfactant
solution, and formed into large (for example, 600 lb.) cakes by placing the wet fibers
into a rotating rub and mechanically stamping the wet mixture to make the cakes as
uniform as possible. The mixture is then pressed in a hydraulic press to form a compressed
cake of fibers having the appearance of a large doughnut.
[0015] The doughnut shaped cakes are stacked in a cage and placed in a kier where they are
subjected to a standard scouring and bleaching step. The cakes are then removed from
the kier, and each cake is dewatered, for example, by placing it in a hydroextractor
and spinning to remove as much water as possible. The dewatered cakes are put in a
cake attacker or wet picker and broken up into small wet tufts. At this stage, the
finish solution containing the durable press resin, lubricant, and catalyst is applied
to the fibers by spraying or immersion, and the fibers are then fed into a drier where
they are dried and cured. Alternatively, the dewatered cakes can be directly immersed
in a finish bath, then separated and formed in a mat for drying and curing. The fibers
can be further processed through an opener to fluff them into individual fibers as
much as possible, then baled and wrapped for shipment.
[0016] An important factor to achieving the improved fiber resiliency in the invention is
that the resin saturates and is cured and crosslinked to the interior of the fibers
while the lubricant stays at or near the surface of the fibers. As depicted in Fig.
2, a cotton fiber has an outer sheath and an interior core (lumen). The cotton fibers
are scoured and bleached to remove their natural surface repellancy, and to render
them absorbent so that they will quickly absorb the resin into the interior of the
fibers. The lubricant will also tend to be absorbed into the fibers. Therefore, the
resin is selected to have a smaller molecular structure than the lubricant, so that
it is more readily absorbed into the interior while the lubricant stays on the surface
of the fibers. If the fibers are dried and allowed to sit for an extended time prior
to curing, for example, more than seven or eight hours, the lubricant may be gradually
absorbed into the interior of the fibers. This would reduce the desired resilient
properties of the fibers. Moreover, the lubrication of the fibers would be reduced.
Therefore, the curing of the fibers must follow the drying of the fibers within a
relatively short period of time.
[0017] The finish solution applied to the fibers in the above-described processes preferably
contains 1.0% - 4.0% formaldehyde-free alkylated glyoxyl/cyclic urea condensate resin,
with 2.5% - 4.0% being the most preferred range, 1.5% - 2.5% reactive silicone, and
0.6% - 0.7% magnesium chloride hexahydrate as the catalyst in water as the carrying
medium. Formaldehyde-free alkylated glyoxyl/cyclic urea condensate resins are obtained,
as disclosed in U.S. Patent 4,345,063 of North, by reacting cyclic urea and glyoxyl
in the presence of a catalyst to yield a water-soluble oligomer condensate. The condensate
is then wholly or partly alkylated by reacting it with an alcohol. Alternatively,
glyoxal is reacted with an alkylated cyclic urea. The reaction product is a formaldehyde-free
resin suitable for application as a finish to cellulose fibers as described above.
Other resins which can be used include melamine resin, as well as formaldehyde-containing
resins, such as glyoxyl (DMDHEU) resin. However, the latter are not as desirable for
home furnishing or skin-contacting products because they can release formaldehyde.
The resin should also be selected so that it does not bond the fibers together.
[0018] The lubricant is selected to have a lubricity which can overcome the interfiber surface
friction, as well as a larger molecular structure than the resin. A reactive silicone
can suitably be used, particularly an amino-functional group silicone, since it has
an affinity for and tends to readily cover the hairy, scaly points on the surface
of the cotton fibers. Other lubricants which can be used include stearates, such as
butoxyethylstearate, or fatty acids. The catalyst is provided to promote cross-linking
of the resin to the fibers. Preferred catalysts include metal salts, such as magnesium
chloride hexahydrate.
[0019] The drying step can be carried out with dry cans providing radiant heat, or with
forced hot air or an oven. The fibers are dried to 5% or less moisture before starting
curing. Curing can be carried out from about 280 degrees to about 360 degrees Fahrenheit,
and the curing time can vary from about 30 to 60 seconds depending on temperature.
The preferred curing temperature is about 300 to 320 degrees. A curing temperature
above 360 degrees may cause browning or yellowing of the silicone or resin finish
on the cotton fibers.
[0020] The resultant finish-treated fibers are found to have an improved resiliency as measured
by the compression-regain method of resiliency measurement. Referring to Fig. 3, the
measurement is taken by compressing a sample of fibers in a cylinder with a plunger.
For the comparative tests herein a one gram fiber sample is formed into a sliver and
inserted into a standard 3/4 inch test tube. With the tube in a vertical position,
a plunger with a one-pound weight attached is inserted in the tube and compresses
the fiber sample under gravity. After a waiting period (5 minutes), the compressed
height of the fibers is measured, and the plunger is removed. Following a recovery
period (5 minutes), the recovery height of the fibers is measured. The difference
between the compressed height and the recovery height is taken as a measurement of
fiber resiliency.
[0021] Examples of cotton fibers treated with a range of finish formulations in accordance
with the invention are shown in Table I below. The alkylated glyoxyl/cyclic urea condensate
resin used was ZF-4, as sold by Sequa Chemicals of Chester, South Carolina. The silicone
used was Sequa Soft-89 silicone, and the catalyst was #531, 30% magnesium chloride
hexahydrate solution, also sold by Sequa Chemicals. As comparative examples, cotton
fibers treated only with a surfactant (S634 cationic soap from Sequa Chemicals) and
polyester fibers (PET) were also measured for resiliency.
TABLE I
| |
#1 |
#2 |
#3 |
#4 |
#5 |
#6 |
| Fibers: |
Cotton |
Cotton |
Cotton |
Cotton |
Cotton |
PET |
| Resin: |
3.0% |
4.0% |
3.0% |
|
3.0% |
|
| Silicone: |
1.5% |
2.0% |
2.5% |
|
1.5% |
|
| Catalyst: |
0.6% |
0.7% |
0.6% |
|
0.6% |
|
| Surfactant: |
|
|
|
0.2% |
|
|
[0022] As shown in the graph of Fig. 4, the treated cotton fibers of Table I had a resiliency
measured as 4.1 - 5.8 cm. or more of recovery, compared to 2.4 cm. for untreated (surfactant
only) cotton fibers and 4.1 cm. for polyester fibers. Thus, the resin/silicone finish
treatment provided a superior resiliency to the cotton fibers comparable to or substantially
greater than that of polyester fibers. Other tests of treated cotton fiber using lesser
amounts of resin than 3.0% also showed an improved resiliency over unfinished cotton
fibers, though not as high as polyester fibers. Similar results can be obtained for
other types of cellulosic fibers, such as cotton linters, and other fibers.
[0023] The durable press resin/lubricant treated fibers of the invention have the properties
of increased resiliency as well as lubrication to allow them to slide easily over
each other to maximize the resiliency effect. Treatment with resin alone will impart
lesser resiliency properties to the cotton fibers, in the range of one-third to one-half
that of the cotton fibers treated with resin and lubricant. The bleached cotton fibers
tended to have 100% pickup of resin and lubricant from the finish solution. The resulting
treated fibers therefore preferably have about 0.675 - 1.8 grams of resin per 100
grams of fiber. The preferred range of silicone was about 0.13 - 1.125 grams to 100
grams of fiber. The use of formaldehyde-free alkylated glyoxyl/cyclic urea condensate
resin also resulted in almost a complete absence of formaldehyde from the finish,
i.e. below trace amounts. The absence of formaldehyde permits the treated fibers to
be safely used as fiber fill material for home furnishing products and other uses
which involve skin contact.
[0024] The increased resiliency of the finish-treated fibers further results in an enhanced
softness and an increased void volume being maintained around the fibers. Thus, the
treated fibers can be advantageously used to form soft, hi-loft fill layers in laminates
and fabrics. The resilient fibers can also be used to form highly absorbent layers
due to their maintenance of the void volume around the fibers and the capacity to
absorb and retain moisture in the void volume. For example, the resilient fibers can
be mixed with absorbent fibers, such as wood pulp fibers, superabsorbent polymer particles
or other absorbent materials. The resilient fibers maintain the void volume used by
the absorbent materials to absorb moisture, thereby enhancing the absorptive capacity
of the layer. If the fibers are treated with a hydrophilic lubricant, such as glycerine
or butoxyethylstearate, the absorption capacity of the fibers is retained, thereby
increasing the total absorptive capacity of the layer.
[0025] An absorbent layer structure using the resilient finish-treated fibers can have
greater absorbency than a conventional superabsorbent layer using untreated cotton
fibers and even synthetic fibers, due to the enhanced resiliency and lofted volume
of the finish-treated fibers. Suitable applications for the absorbent layer structure
include diaper absorbent sheets, sanitary napkins, absorbent sheets, tissues, towels,
etc.
[0026] It is to be understood that although preferred embodiments of the invention have
been described, numerous modifications and variations are of course possible within
the principles of the invention. All such embodiments, modifications, and variations
are considered to be within the spirit and scope of the invention as defined in the
claims appended hereto.
1. A method of treating individual fibers to have an improved resiliency, characterized
by saturating the individual fibers with a finish solution of a durable press resin
and a lubricant such that the resin saturates to the interior of the fibers while
the lubricant is retained at or near the surface of the fibers, and drying and curing
the resin to be cross-linked to the fibers before the lubricant can be absorbed into
the interior of the fibers.
2. The method of claim 1, characterized by the fact that the lubricant is selected
to have a larger molecular structure than that of the resin, so that the resin is
absorbed more readily into the interior of the fibers than the lubricant.
3. The method of claim 1, characterized by the fact that the fibers to be finish-treated
are scoured and bleached cotton fibers.
4. The method of claim 1, characterized by the fact that the durable press resin is
an alkylated glyoxyl/cyclic urea condensate resin.
5. The method of claim 5 characterized by the fact that the resin is provided in an
amount of 3.0% - 4.0% of the finish solution.
6. The method of claim 1, characterized by the fact that the lubricant is a amino-functional
group silicone.
7. The method of claim 6, characterized by the fact that the silicone is provided
in an amount of 1.5 - 2.5% of the finish solution.
8. The method of claim 1, characterized by the fact that the finish solution further
includes a catalyst to promote cross-linking of the resin.
9. The method of claim 8, characterized by the fact that the catalyst is 30% magnesium
chloride hexahydrate solution provided in an amount of 0.6% - 0.7% of the finish solution.
10. The method of claim 1 adapted for treating cotton fibers, characterized by the
fact that it further comprises a continuous process of forming a carded mat of cotton
fibers, scouring and bleaching the cotton fiber mat, then saturating the cotton fiber
mat with the finish solution, then drying and curing the fibers.
11. The method of claim 1 adapted for treating cotton fibers, characterized by the
fact that it comprises a batch process of forming compressed cakes of cotton fibers,
scouring and bleaching the cotton fiber cakes in a kier, dewatering the cleaned cotton
fiber cakes, separating the cotton fibers into small tufts, applying the finish solution
to the cotton fibers, then drying and curing the fibers.
12. A finish-treated fiber product comprising individual fibers having a finish of
a durable press resin and a lubricant, characterized by the fact that the resin is
saturated and cured and cross-linked into the interior of the fibers while the lubricant
is maintained at or near the surface of the fibers, such that the finish-treated fibers
have an improved resiliency over untreated fibers.
13. The improved fiber product of claim 12, characterized by the fact that the lubricant
is selected to have a larger molecular structure than that of the resin, so that the
resin is absorbed more readily into the interior of the fibers than the lubrican.
14. The improved fiber product of claim 12, characterized by the fact that the fibers
are cotton fibers.
15. The improved fiber product of claim 14, characterized by the fact that the resin
is a formaldehyde-free alkylated glyoxyl/cyclic urea condensate resin.
16. The improved fiber product of claim 15, characterized by the fact tht the cotton
fibers have a finish of 0.675 - 1.8 grams of formaldehyde-free alkylated glyoxal/cyclic
urea condensate resin per 100 grams of fiber, and about 0.13 - 1.125 grams of an amino-functional
group silicone as the lubricant to 100 grams of fiber.
17. The improved fiber product of claim 15, characterized by the fact that the finish-treated
fibers have a resiliency of about 4.1 - 5.8 centimeters or more of recovery after
initial compression, using a compression-regain testing method, as compared to about
4.1 centemeters for polyester fibers.
18. The improved fiber product of claim 12, characterized by the fact that the finish-treated
fibers are used as a fiber fill material.
19. The improved fiber product of claim 12, characterized by the fact that the finish-treated
fibers are used to form an absorbent layer.
20. The improved fiber product of claim 12, characterized by the fact tht the lubricant
is a hydrophilic lubricant.