U.S. patent application number 10/155534 was filed with the patent office on 2003-04-03 for thermoadhesive conjugate fibers and nonwoven fabric employing them.
This patent application is currently assigned to CHISSO CORPORATION. Invention is credited to Iwata, Masuo, Nakai, Yoshihiro.
Application Number | 20030064651 10/155534 |
Document ID | / |
Family ID | 19002202 |
Filed Date | 2003-04-03 |
United States Patent
Application |
20030064651 |
Kind Code |
A1 |
Nakai, Yoshihiro ; et
al. |
April 3, 2003 |
Thermoadhesive conjugate fibers and nonwoven fabric employing
them
Abstract
To provide thermoadhesive conjugate fibers, nonwoven fabrics and
cellulosic fiber blended nonwoven fabrics employing them, and
wipers and absorbers employing the fabrics, thermoadhesive
conjugate fibers comprise a thermoplastic resin (I) containing a
modified polyolefin with at least one type of reactive functional
group as a first component and having a second component composed
of a thermoplastic resin (II) with a higher melting point than the
thermoplastic resin (I) of the first component combined in a
conjugate therewith, the first component being formed continuously
along the length of at least a portion of the fiber surface,
wherein the fiber surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group of the modified polyolefin.
Inventors: |
Nakai, Yoshihiro;
(Osaka-shi, JP) ; Iwata, Masuo; (Moriyama-shi,
JP) |
Correspondence
Address: |
MERCHANT & GOULD PC
P.O. BOX 2903
MINNEAPOLIS
MN
55402-0903
US
|
Assignee: |
CHISSO CORPORATION
6-32, Nakanoshima 3-chome, kita-ku
Osaka-shi
JP
|
Family ID: |
19002202 |
Appl. No.: |
10/155534 |
Filed: |
May 24, 2002 |
Current U.S.
Class: |
442/361 ;
428/364; 428/373; 428/375; 442/153 |
Current CPC
Class: |
Y10T 442/291 20150401;
D04H 1/02 20130101; D04H 1/5418 20200501; D04H 1/732 20130101; B32B
2262/0253 20130101; D06M 15/643 20130101; D04H 1/54 20130101; Y10T
428/2929 20150115; Y10T 428/2933 20150115; D04H 1/43835 20200501;
D04H 1/544 20130101; B32B 2262/062 20130101; B32B 2262/12 20130101;
D04H 1/5412 20200501; Y10T 442/277 20150401; D04H 1/50 20130101;
D06M 13/148 20130101; Y10T 428/2913 20150115; B32B 27/12 20130101;
D04H 1/425 20130101; D06M 13/368 20130101; B32B 5/022 20130101;
D06M 13/292 20130101; D04H 1/43828 20200501; D04H 1/55 20130101;
D04H 1/74 20130101; Y10T 442/637 20150401; D06M 13/332 20130101;
B32B 2432/00 20130101; D01F 8/06 20130101; D04H 1/43832 20200501;
D04H 1/4291 20130101; D06M 15/03 20130101; D06M 13/188 20130101;
B32B 27/32 20130101; D04H 1/5414 20200501; B32B 2262/0276
20130101 |
Class at
Publication: |
442/361 ;
428/364; 428/373; 428/375; 442/153 |
International
Class: |
B32B 009/04; D04H
001/00 |
Foreign Application Data
Date |
Code |
Application Number |
May 28, 2001 |
JP |
2001-158484 |
Claims
What is claimed is:
1. Thermoadhesive conjugate fibers which are fibers comprising a
thermoplastic resin (I) containing a modified polyolefin with at
least one type of reactive functional group as a first component
and having a second component composed of a thermoplastic resin
(II) with a higher melting point than the thermoplastic resin (I)
of the first component combined in a conjugate therewith, the first
component being formed continuously along the length of at least a
portion of the fiber surface, wherein said fiber surfaces are
coated with a fiber treating agent containing a multifunctional
compound capable of reacting with the reactive functional group of
the modified polyolefin.
2. Thermoadhesive conjugate fibers according to claim 1, wherein
the modified polyolefin is a copolymer of an olefin monomer and an
unsaturated carboxylic acid or its derivative.
3. Thermoadhesive conjugate fibers according to claim 1, wherein
the modified polyolefin is a copolymer of polyethylene and an
unsaturated carboxylic acid or its derivative.
4. Thermoadhesive conjugate fibers according to claim 1, wherein
the thermoplastic resin (II) is polypropylene.
5. Thermoadhesive conjugate fibers according to claim 1, wherein
the thermoplastic resin (II) is a polyester.
6. Thermoadhesive conjugate fibers according to claim 1, wherein
the multifunctional compound is a polyhydric alcohol.
7. Thermoadhesive conjugate fibers according to claim 1, wherein
the multifunctional compound is a polyamine.
8. A nonwoven fabric comprising thermoadhesive conjugate fibers
which are fibers comprising a thermoplastic resin (I) containing a
modified polyolefin with at least one type of reactive functional
group as a first component and having a second component composed
of a thermoplastic resin (II) with a higher melting point than the
thermoplastic resin (I) of the first component combined in a
conjugate therewith, the first component being formed continuously
along the length of at least a portion of the fiber surface,
wherein said fiber surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group of the modified polyolefin.
9. A cellulosic fiber blended nonwoven fabric composed of
cellulosic fibers and thermoadhesive conjugate fibers which are
fibers comprising a thermoplastic resin (I) containing a modified
polyolefin with at least one type of reactive functional group as a
first component and having a second component composed of a
thermoplastic resin (II) with a higher melting point than the
thermoplastic resin (I) of the first component combined in a
conjugate therewith, the first component being formed continuously
along the length of at least a portion of the fiber surface,
wherein said fiber surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group of the modified polyolefin.
10. A nonwoven fabric composed of thermoadhesive conjugate fibers
which are fibers comprising a thermoplastic resin (I) containing a
modified polyolefin with at least one type of reactive functional
group as a first component and having a second component composed
of a thermoplastic resin (II) with a higher melting point than the
thermoplastic resin (I) of the first component combined in a
conjugate therewith, the first component being formed continuously
along the length of at least a portion of the fiber surface,
wherein said fiber surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group of the modified polyolefin, and wherein
the nonwoven fabric is produced by an air-laid method.
11. A cellulosic fiber blended nonwoven fabric composed of
cellulosic fibers and thermoadhesive conjugate fibers which are
fibers comprising a thermoplastic resin (I) containing a modified
polyolefin with at least one type of reactive functional group as a
first component and having a second component composed of a
thermoplastic resin (II) with a higher melting point than the
thermoplastic resin (I) of the first component combined in a
conjugate therewith, the first component being formed continuously
along the length of at least a portion of the fiber surface,
wherein said fibers surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group of the modified polyolefin, and wherein
the cellulosic fiber blended nonwoven fabric is produced by an
air-laid method.
12. A wiper employing a nonwoven fabric or cellulosic fiber blended
nonwoven fabric according to any one of claims 8 to 11.
13. An absorber employing a nonwoven fabric or cellulosic fiber
blended nonwoven fabric according to any one of claims 8 to 11.
Description
FIELD OF INVENTION
[0001] The present invention relates to thermoadhesive conjugate
fibers with satisfactory thermoadhesive properties, to nonwoven
fabrics and cellulosic fiber blended nonwoven fabrics employing
them and to wipers and absorbers employing the fabrics.
BACKGROUND OF THE INVENTION
[0002] Thermoadhesive conjugate fibers having a conjugate form
comprising on the fiber surface a low-melting-point component made
of polyethylene, a ethylene-propylene-butene copolymer or
crystalline polypropylene, and at the fiber center a
high-melting-point component made of an ethylene-propylene-butene
copolymer, crystalline polypropylene or a polyester, are widely
known.
[0003] Such thermoadhesive conjugate fibers are usually formed into
a web and then heated at a temperature above the melting point of
the low-melting-point component and below the melting point of the
high-melting-point component to allow formation of a nonwoven
fabric wherein the contacting sections between the fibers composing
the web are fused together.
[0004] However, because such thermoadhesive conjugate fibers have
low adhesion for other materials (for example, cloth, wood or
metal), it is necessary to use a binder (for example, polyvinyl
alcohol or the like) to improve the adhesion when the nonwoven
fabric is to be employed for obtaining a conjugate material bonded
to another material or for blending with other materials to obtain
cellulosic fiber blended nonwoven fabrics. When such a binder is
used, however, the (cellulosic fiber blended) nonwoven fabric
surface becomes coated with the binder to form a film, and this has
caused problems such as reduced performance (absorption properties,
etc.) of the (cellulosic fiber blended) nonwoven fabric, or in the
case of a thick (cellulosic fiber blended) nonwoven fabric, seepage
of the binder into the interior resulting in interlayer peeling of
the (cellulosic fiber blended) nonwoven fabric.
[0005] In recent years, several processes have been developed for
the purpose of improving the adhesion in order to overcome these
problems (Japanese Patent Application Laid-Open No. 53-126320,
Japanese Patent Application Laid-Open No. 54-30929, Japanese Patent
Application Laid-Open No. 2000-212866, U.S. Pat. Nos. 4,950,541,
5,981,410). However, it is currently the situation that all of
these processes still produce inadequate fiber strength or nonwoven
fabric strength, despite providing satisfactory adhesion with other
materials.
SUMMARY OF THE INVENTION
[0006] It is an object of the present invention to provide novel
thermoadhesive conjugate fibers which have excellent adhesion with
other materials while also allowing the obtained nonwoven fabrics
to exhibit sufficient strength. It is another object to provide
thermoadhesive conjugate fibers which, when blended with other
materials (for example, cellulosic fibers) to obtain cellulosic
fiber blended nonwoven fabrics, exhibit firm adhesion with the
other materials to prevent peeling or losing from the other
materials, and provide sufficient strength to prevent tearing. It
is yet another object to provide nonwoven fabrics and cellulosic
fiber blended nonwoven fabrics having the aforementioned
characteristics and wipers and absorbers that employ the
fabrics.
[0007] As a result of much diligent research, the present inventors
have completed the present invention upon finding that excellent
adhesion with other materials (particularly cellulosic fibers) and
high nonwoven fabric strength are exhibited by thermoadhesive
conjugate fibers wherein the surfaces of thermoadhesive conjugate
fibers employing a modified polyolefin which includes a reactive
functional group are coated with a fiber treating agent containing
a multifunctional compound capable of reacting with the reactive
functional group.
DETAILED DESCRIPTION OF THE INVENTION
[0008] The thermoadhesive conjugate fibers of the invention
comprise a thermoplastic resin (I) containing a modified polyolefin
with at least one type of reactive functional group as a first
component and a thermoplastic resin (II) with a higher melting
point than the first component as a second component, and it is
characterized in that the first component is formed continuously
along the length of at least a portion of the fiber surface, and
the fiber surfaces are coated with a fiber treating agent
containing a multifunctional compound capable of reacting with the
reactive functional group in the modified polyolefin.
[0009] The reactive functional group of the modified polyolefin
contained in the thermoplastic resin (I) as the first component may
be appropriately selected in consideration of the reactivity with
the multifunctional compound in the fiber treating agent, and it is
not particularly restricted. Specifically there may be mentioned as
examples hydroxyl, amino, nitrile, nitro, amide, carbonyl, carboxyl
and glycidyl groups.
[0010] The modified polyolefin with the reactive functional group
may be obtained by copolymerizing a vinyl monomer having the
reactive functional group with an olefin monomer. The modified
polyolefin may be a block, random or ladder copolymer. The vinyl
monomer may alternatively be graft copolymerized in the
polyolefin.
[0011] As vinyl monomers with reactive functional groups there may
be mentioned unsaturated carboxylic acids such as maleic acid,
acrylic acid, methacrylic acid, fumaric acid and itaconic acid, or
derivatives thereof or their anhydrides, styrenes such as styrene
and -methylstyrene, methacrylic acid esters such as methyl
methacrylate, ethyl methacrylate, 2-hydroxyethyl methacrylate and
dimethylaminoethyl methacrylate, or the corresponding acrylate acid
esters, as well as glycidyl acrylate, glycidyl methacrylate,
butenecarboxylic acid esters, allyl glycidyl ether,
3,4-epoxybutene, 5,6-epoxy-1-hexene and vinylcyclohexene
monoxide.
[0012] The modified polyolefin to be used for the invention is
preferably a modified polyolefin obtained by graft copolymerization
of a vinyl monomer composed of an unsaturated carboxylic acid or
its derivative or anhydride, with a polyolefin, from the standpoint
of common usage and easy obtainment, and achieving affinity with
numerous types of other materials and particularly satisfactory
adhesion with hydroxyl group-containing materials such as
cellulosic fibers.
[0013] Such modified polyolefins are preferred because they are
easily worked into fibers and exhibit high polymer strength,
yielding high strength as fibers.
[0014] The modification ratio is preferably at least 0.1 mole/kg in
order to improve the reactivity with the multifunctional compound
in the fiber treating agent and create a more extensive crosslinked
structure.
[0015] Ethylene, propylene, butene-1 or the like is preferably used
as the main monomer for the modified polyolefin.
[0016] When the modified polyolefin is a graft copolymer with the
vinyl monomer, the main polymer of the modified polyolefin (the
polyolefin before modification) is preferably polyethylene,
polypropylene, polybutene-1 or the like, and high-density, linear
low-density or low-density polyethylene is particularly
preferred.
[0017] When polyethylene is used as the main polymer, an ethylene
polymer or a copolymer of ethylene with another -olefin, having a
density of 0.90-0.97 g/cm.sup.3 and a melting point of about
100-135.degree. C., is preferred.
[0018] When polypropylene is used as the main polymer, crystalline
propylene polymer or a copolymer of propylene with another olefin,
having a melting point of 130-170.degree. C., is preferred.
[0019] When polybutene-1 is used as the main polymer, crystalline
butene-1 polymer or a copolymer of butene-1 with another olefin,
having a melting point of 110-130.degree. C., is preferred.
[0020] Among these polymers, polyethylene is preferred from the
standpoint of ease of utilization as a low-melting-point component
and ease of modifying vinyl monomers, and high-density polyethylene
is more preferred because of its high polymer strength which allows
improvement in nonwoven fabric strength.
[0021] The thermoplastic resin (I) of the first component is not
particularly restricted so long as it contains the aforementioned
modified polyolefin, and it may be a simple modified polyolefin, a
blend of two or more modified polyolefins, or a blend of at least
one type of modified polyolefin with at least one type of other
thermoplastic resin.
[0022] When the modified polyolefin is a graft copolymer, the
polymer will tend to have lower polymer strength than the main
polymer due to the graft copolymerization. Thus, in order to
maintain high fiber strength the thermoplastic resin (I) is
preferably a blend of a modified polyolefin having a high
modification ratio with a polyolefin that has not been
modified.
[0023] The thermoplastic resin (II) used according to the invention
is a thermoplastic resin with a higher melting point than the
thermoplastic resin (I). As such thermoplastic resins there may be
preferably used, for example, polypropylene, polyethylene,
copolymers of ethylene, propylene, .alpha.-olefins and the like,
and crystalline polymers of polyester, polyamide and the like.
[0024] If the thermoplastic resin (II) has a high melting point
against thermoplastic resin (I), a blend of a plurality of
thermoplastic resins may be used as the thermoplastic resin (II)
instead of a single type. The thermoplastic resin (II) is
preferably a polyolefin from the standpoint of chemical resistance
and compatibility with the modified polyolefin, and it is
preferably high-melting-point polypropylene which gives a higher
difference in melting point with the thermoplastic resin (I), from
the standpoint of workability when obtaining nonwoven fabrics or
cellulosic fiber blended nonwoven fabrics by thermoadhesive between
fibers. Polyesters are also preferred for use because of their high
melting points.
[0025] There may also be appropriately added to the thermoplastic
resin (I) of the first component and the thermoplastic resin (II)
of the second component, additives which exhibit various types of
performance depending on the need, such as antioxidants,
photostabilizers, ultraviolet absorbers, neutralizers, nucleating
agents, epoxy stabilizers, lubricants, anti-fungus agents, flame
retardants, antistatic agents, pigments, plasticizers and the like,
within ranges that do not impede the effect of the invention.
[0026] The thermoadhesive conjugate fibers of the invention must
have the first component formed on at least a portion of the fiber
surface. Such conjugate fibers may be obtained using a spinning
pack for side-by-side type, core/sheath type or eccentric
core/sheath type fibers having the first component as the sheath
and the second component as the core.
[0027] The cross-sectional shape of the thermoadhesive conjugate
fibers of the invention may have any of various forms, for example,
round such as circular or oval, polygonal such as square or
triangular, or irregular such as key-shaped or eight branch
leaf.
[0028] The thermoadhesive conjugate fibers of the invention will
have adhesive force for other materials even if the first component
is formed on a small portion of the fiber surface, but for
satisfactory adhesive force it is preferred for the ratio of
circumferences in the fiber cross-section to be 50%. Thermoadhesive
conjugate fibers having a core/sheath structure with a ratio of
circumferences in the fiber cross-section of 100% or nearly 100%
are particularly preferred to exhibit especially strong adhesive
force.
[0029] The thermoadhesive conjugate fibers of the invention will be
spinnable so long as the component ratio of the first component and
second component of the fiber cross-section is in the range of
10/90 to 90/10. When the first component is reduced the adhesion is
lower and when it is increased the adhesion points become firmer,
and therefore the component ratio may be determined in
consideration of the desired adhesive force; however, a component
ratio of 30/70 to 70/30 is preferred for preventing reduced
conjugate fiber strength and fiber workability.
[0030] The thermoadhesive conjugate fibers of the invention may be
spun with an ordinary melt spinning machine. The spinning
temperature will differ depending on the thermoplastic resin used,
but will normally be carried out in the range of 180-350.degree. C.
However, the first component is preferably spun at a low
temperature in order to minimize decomposition and deterioration of
the modified polyolefin in the first component.
[0031] The size of the as-spun fiber may be appropriately selected
depending on the need.
[0032] The as-span fiber obtained by the spinning is drawn at a
lower temperature than the melting point of the first component
(usually 40-120.degree. C.) to any desired draw ratio (usually
2-6), and then crimped if necessary. There is no particular
requirement either for crimping or no crimping, as it is sufficient
to achieve a shape suitable for nonwoven fabric working. For
example, when using thermoadhesive conjugate fibers by an air-laid
method, there is no particular need for crimping of the fibers,
although normally the fibers used will have crimping of 0-20
crimps/2.54 cm. On the other hand, when using thermoadhesive
conjugate fibers by a carding method, crimping of the fibers is
essential, and the fibers used will normally have crimping of 5-30
crimps/2.54 cm. The crimping of the fibers may be mechanical
crimping with a machine, or crimping arising by actual or latent
crimping of the conjugate fibers themselves.
[0033] The thermoadhesive conjugate fibers which have been drawn
and then crimped are usually cut to a desired length. The cutting
method and the length of the fibers are not particularly restricted
so long as they result in a length suited for nonwoven fabric
working.
[0034] The thermoadhesive conjugate fibers of the invention are
usually used with fiber fineness of 0.5-100 dtex, but there is no
particular restriction in this regard. For increased nonwoven
fabric strength, a thinner fiber fineness will generally result in
more fibers and adhesive point per given area, and a fiber fineness
of 0.5-10 dtex is therefore preferred.
[0035] The fiber treating agent used for the invention is not
particularly restricted so long as it contains a multifunctional
compound (a compound having two or more functional groups such as
hydroxyl, amino, nitrile, nitro, amide, carbonyl, carboxyl or
glycidyl groups per molecule) that can react with the reactive
functional group of the modified polyolefin in the first component,
and compounds composed of mixtures of polyhydric alcohols,
polyamines, polycarboxylic acids and hydroxyl groups are preferred
in consideration of safety, handleability and reactivity with the
modified polyolefin.
[0036] Polyhydric alcohols are alcohols having two or more hydroxyl
groups per molecule. Polyamines are aliphatic compounds having two
or more amino groups (--NH.sub.2) or imino groups (.dbd.NH), but
according to the invention, compounds having two or more
--NR.sub.2, --RNH or --NH.sub.2 groups per molecule may also be
used.
[0037] The multifunctional compound will usually be diluted with
water for use, and is therefore preferably a water-soluble
compound, of which there may be mentioned glycerin, ethylene
glycol, ethylenediamine, diethylenetriamine, maleic acid and
triethanolamine.
[0038] The fiber treating agent used for the invention may consist
only of the aforementioned multifunctional compound, but may also
contain esters, for example, aliphatic esters such as 2-ethylhexyl
stearate or isopropyl myristate, as lubricating agents, natural
oils and fats such as coconut oil or beef tallow, anionic
surfactants as antistatic agents, for example, alkyl sulfates,
fatty acid soaps, alkyl sulfonates, alkylphosphoric acid esters and
the like, as well as antioxidants, preservatives, rust preventives,
antifungal agents, wettability enhancers and the like, within a
range that does not inhibit the effect of the invention.
[0039] There are no particular restrictions on the process for
coating the thermoadhesive conjugate fibers with the fiber treating
agent, and any common publicly known method may be utilized. For
example, a coating method using a touch roll, spraying, immersion
or the like may be employed during the spinning step, drawing step,
cutting step or later steps.
[0040] The coating coverage is usually preferred to be in the range
of 0.1-2.0 wt % of the fiber treating agent solid matter with
respect to the weight of the fibers. The coating coverage of the
multifunctional compound in the fiber treating agent is sufficient
at 0.005% or more with respect to the fiber weight, and there is no
problem with a greater degree of coating coverage.
[0041] Since the thermoadhesive conjugate fibers of the invention
have a modified polyolefin with the aforementioned reactive
functional group in the first component, where the fiber surfaces
are coated with a fiber treating agent containing a multifunctional
compound that is reactive with the reactive functional group, heat
treatment of the fibers causes reaction between the reaction
functional group in the modified polyolefin and the multifunctional
compound in the fiber treating agent, forming a reticulate
structure (a crosslinked structure) with the modified polyolefin.
This can be confirmed by the reduced melt flow rate (higher melt
viscosity) of the thermoadhesive conjugate fibers after coating of
the fiber treating agent and heat treatment, as compared to
thermoadhesive conjugate fibers which are not coated with a fiber
treating agent. Thus, the thermoadhesive conjugate fibers of the
invention are advantageous for production of high-strength nonwoven
fabrics, since crosslinking reaction occurs at the adhesive point
between the thermoadhesive conjugate fibers resulting in firm
adhesion points, and fiber deformation (variation in the fiber
cross-sectional area due to melting and flow off of the fiber
surface by heating) caused by high temperature treatment can be
minimized, thus preventing very small fiber cross-sections and
avoiding reduced strength of the fibers themselves. In addition,
the thermoadhesive conjugate fibers of the invention also have
highly satisfactory adhesion with other materials, and thus for
example, when blended with cellulosic fibers and the like, are able
to greatly minimize peeling and losing.
[0042] A nonwoven fabric of the invention is obtained using the
thermoadhesive conjugate fibers of the invention, but other
thermoadhesive conjugate fibers may also be included depending on
the need, so long as the effect of the invention is not
impeded.
[0043] A nonwoven fabric according to the invention may be obtained
by forming a web of the thermoadhesive conjugate fibers of the
invention and subjecting the web to heat treatment. The working
method used in this case may be a commonly used one such as carding
or air-laying, but when employing a working method such as sheeting
or spun lacing, whereby the fiber treating agent coated onto the
thermoadhesive conjugate fiber surface flows off, it is necessary
to include means such as preheating treatment to prevent flow off
of the fiber treating agent.
[0044] A cellulosic fiber blended nonwoven fabric according to the
invention is obtained using thermoadhesive conjugate fibers
according to the invention and cellulosic fibers, but other
thermoadhesive conjugate fibers may also be included if necessary
so long as the effect of the invention is not impeded.
[0045] A cellulosic fiber blended nonwoven fabric according to the
invention may be obtained by the same working methods as described
above for nonwoven fabrics, but an air-laid method is preferred for
easier uniform dispersion of the thermoadhesive conjugate fibers
and cellulosic fibers in order to achieve a satisfactory texture
and feel of the cellulosic fiber blended nonwoven fabric.
[0046] The blending ratio of the thermoadhesive conjugate fibers
(A) and cellulosic fibers (B) is not particularly restricted, and
other fibers, fillers or super-absorbent resins may also be
included so long as the effect of the invention is not impeded;
however, if the proportion of the thermoadhesive conjugate fibers
(A) is too low, the strength of the nonwoven fabric is reduced,
whereas an increasing proportion of the thermoadhesive conjugate
fibers (A) prevents clear expression of the properties of the
cellulosic fibers (B), and therefore the preferred construction is
3-90 wt % of the thermoadhesive conjugate fibers (A) and 10-97 wt %
of the cellulosic fibers (B).
[0047] An air-laid method as a working method suited for adequately
exhibiting the effect of the invention will be characterized by
using staple fibers, and will generally be carried out by the
following procedure.
[0048] First, the staple fibers obtained by cutting the
thermoadhesive conjugate fibers of the invention to about 5 mm are
loaded into an opening machine for mechanical opening, and are then
sent to a fiber feeding circulating duct. In order to obtain a
cellulosic fiber blended nonwoven fabric, pulp (consisting of
cellulosic fibers) is simultaneously crushed with a crusher, and
the fibers are sent to the fiber feeding circulating duct. In the
fiber feeding circulating duct, the staple fibers and pulp are
blended and passed through a forming head to produce aggregated
fibers. Forming heads of various shapes exist, but typically the
blended aggregated fibers are lowered with a screen member on a
drum, and suction is applied with a suction apparatus to produce
build-up and form a web. The screen member referred to here is a
mesh with round- or square-shaped holes.
[0049] Since the staple fibers in the web of the cellulosic fiber
blended nonwoven fabric of the invention are uniformly dispersed,
the texture and feel is superior to conventional pulp blended
nonwoven fabrics, and the strength is higher due to the uniform
presence of adhesion points.
[0050] A nonwoven fabric or cellulosic fiber blended nonwoven
fabric according to the invention is easily obtained by heat
treating the web made of the thermoadhesive conjugate fibers. As
heat treatment methods there may be mentioned methods using a hot
air drier, suction band drier or the like. Heat treatment melts the
first component of the thermoadhesive conjugate fibers causing
thermoadhesive at the adhesive point between the thermoadhesive
conjugate fibers (A) or between the thermoadhesive conjugate fibers
(A) and the cellulosic fibers (B). The heat treatment is most
preferably conducted at a temperature above the melting point of
the first component of the thermoadhesive conjugate fibers and
below the melting point of the second component. The heat treatment
time may be adjusted in consideration of the thermal fusion method
used and the weight of the nonwoven fabric or cellulosic fiber
blended nonwoven fabric to be obtained.
[0051] The obtained nonwoven fabric or cellulosic fiber blended
nonwoven fabric may be further heat treated using a hot press or
conveyer-type hot press for adjustment to the desired thickness,
and if necessary, secondary working may be carried out either
during or after the heat treatment to perform molding to a desired
shape.
[0052] The nonwoven fabric or cellulosic fiber blended nonwoven
fabric of the invention may be laminated with another web or sheet
in order to obtain a laminated sheet. Examples of sheet materials
include knitted fabrics, nonwoven fabrics, urethane foam, films,
paper materials, wool molds, metal sheets, wood panels, and plastic
panels, and preferably materials containing OH groups, which may
maintain their respective functions. For example, a cellulosic
fiber blended nonwoven fabric composed of thermoadhesive conjugate
fibers alone or a blend of hydrophilic fibers and thermoadhesive
conjugate fibers may be laminated therewith. Other materials may
also be suitably laminated therewith so long as the effect of the
invention is not impeded.
[0053] A cellulosic fiber blended nonwoven fabric according to the
invention may be used for a variety of purposes, but the high
strength of the nonwoven fabric and its satisfactory adhesion with
cellulosic fibers renders it suitable for such purposes as wipers,
absorbers and the like.
EXAMPLE
[0054] The present invention will now be explained by way of
examples, with the understanding that the invention is in no way
limited by these examples. The property values indicated in the
examples were measured by the following methods.
[0055] Number of crimps: The number of crimps in the thermoadhesive
conjugate fibers was measured according to JIS-L-1015.
[0056] Fiber fineness: The single fiber size of the thermoadhesive
conjugate fibers was measured according to JIS-L-1015.
[0057] Unit weight: A 50 cm square was cut from the nonwoven fabric
or cellulosic fiber blended nonwoven fabric and weighed, and the
weight was expressed per unit area (g/m.sup.2).
[0058] Losing rate of cellulosic fiber: The weight (W1) of a 10 cm
square cut from the cellulosic fiber blended nonwoven fabric was
measured, and it was then mounted on the fly comb of a carding
machine and vibrated for 3 minutes under conditions with an
amplitude of 3 cm and a frequency of 1700 rpm, after which the
weight (W2) was measured and the rate calculated by the following
equation:
[(W1)-(W2)]/(W1).times.100=losing rate (%)
[0059] Specific volume: The specific volume of the nonwoven fabric
or cellulosic fiber blended nonwoven fabric was calculated by the
following equation:
Specific volume (cm.sup.3/g)=Thickness (mm)/unit weight
(g/m.sup.2).times.1000
[0060] Amount of fiber treating agent adhering (%): The fiber
treating agent coated onto 2 g of thermoadhesive conjugate fibers
was extracted by immersion in 25 ml of methanol, and then the
extraction methanol alone was evaporated off, the residue was
weighed and the weight ratio with respect to the fibers was
calculated.
[0061] MFR: The MFR values for the first component and second
component were measured at 230.degree. C. according to
JIS-K-7210.
[0062] Fiber MFR: The MFR of the thermoadhesive conjugate fibers
was measured at 230.degree. C. according to JIS-K-7210. (For
Examples 15 and 16, thermoadhesive fibers obtained with only the
first component were used.)
[0063] MI: The MI values for the first component and second
component were measured at 190.degree. C. according to
JIS-K-7210.
[0064] Nonwoven fabric strength: Three samples were taken from the
nonwoven fabric or cellulosic fiber blended nonwoven fabric with a
CD of 5 cm and an MD of 15 cm. The breaking strength (N/5 cm) of
each of the samples was measured using an AGS500D Autograph by
Shimazu Laboratories, Ltd. under conditions with a clamp spacing of
10 cm and a tensile speed of 10 cm/min, and the average of the
three samples was recorded as the nonwoven fabric strength.
[0065] The machine flow direction (lengthwise direction) of the
nonwoven fabric or cellulosic fiber blended nonwoven fabric was
used as MD, and the direction orthogonal to the machine flow
direction (widthwise direction) was used as CD.
Examples 1-22, Comparative Examples 1-7
[0066] A core/sheath type, side-by-side type or eccentric
core/sheath type spinneret was used to spin conjugate fibers using
a first component and second component under the conditions shown
in Tables 1 and 2, and after drawing, 15 wt % aqueous solutions of
the fiber treating agents shown in Tables 1 and 2 were coated onto
the conjugate fiber surfaces with a touch roll, to obtain
thermoadhesive conjugate fibers. The production conditions and
conjugate fiber properties for the thermoadhesive conjugate fibers
are shown in Table 1 (examples) and Table 2 (comparative
examples).
[0067] The spinning temperatures shown in Tables 1 and 2 are the
spinneret temperatures; the melt temperatures preceding the
spinning pack were 220.degree. C. for the first component, and
250.degree. C. for PP or 310.degree. C. for PET as the second
component. The drawing temperature indicated is the roll
temperature. The other abbreviations are as follows.
[0068] Modified PE1: Polymer comprising high-density polyethylene
with a density of 0.960 g/cm.sup.3 as the backbone polymer and
maleic anhydride at a grafting ratio of 0.3 mole/Kg; MI=3 g/10
min.
[0069] Modified PE2: Polymer comprising high-density polyethylene
with a density of 0.960 g/cm.sup.3 as the backbone polymer and
maleic anhydride at a grafting ratio of 0.15 mole/Kg; MI=10 g/10
min.
[0070] Modified PE3: Polymer comprising linear low-density
polyethylene with a density of 0.931 g/cm.sup.3 as the backbone
polymer and maleic anhydride at a grafting ratio of 0.15 mole/Kg;
MI=14 g/10 min.
[0071] Modified PE4: Terpolymer comprising 78% ethylene, 19.5%
ethylene acrylate and 2.5% maleic anhydride; MI=20 g/10 min.
[0072] Modified PE5: Copolymer of ethylene and glycidyl
methacrylate; MFR=7 g/10 minute.
[0073] Modified PP1: Polymer comprising polypropylene as the
backbone polymer and maleic anhydride at a grafting ratio of 0.15
mole/Kg; MFR=7 g/10 min.
[0074] PP: Crystalline homopolypropylene; MFR=17 g/10 min.
[0075] PET: Polyethylene terephthalate with a melting point of
250.degree. C.
[0076] HDPE: High-density polyethylene with a density of 0.960
g/cm.sup.2; MI=17 g/10 min.
[0077] LLDPE: Linear low-density polyethylene with a density of
0.935 g/cm.sup.3; MI=30 g/10 min.
[0078] co-PP: Propylene copolymer comprising 4.0 wt % ethylene and
2.7 wt % butene-1; MFR=16 g/10 min.
[0079] Fiber treating agent A: Emulsion comprising 60%
polyoxyethylene alkyl ether, 20% alkylphosphate sodium salt and 20%
triethanolamine.
[0080] Fiber treating agent B: Emulsion comprising 60%
polyoxyethylene alkyl ether, 30% alkylphosphate sodium salt and 10%
ethylenediamine.
[0081] Fiber treating agent C: Emulsion comprising 60%
polyoxyethylene alkyl ether, 20% fatty acid, 10% 1,5-pentanediol
and 10% ethylenediamine.
[0082] Fiber treating agent D: Emulsion comprising 60%
polyoxyethylene alkyl ether, 15% alkylphosphate sodium salt, 5%
silicone, 10% glycerin and 10% ethylene glycol.
[0083] Fiber treating agent E: Emulsion comprising 60%
polyoxyethylene alkyl ether, 20% alkylphosphate sodium salt and 20%
1,2-ethanedithiol.
[0084] [Table 1]
[0085] [Table 2]
1 TABLE 1 Number of Fiber Amount Fiber Sheath/ Spinning Drawing
Draw- Fine- crimps treating of fiber MFR First Second core Tempera-
Tempera- ing ness (crimps/ agent treating (g/ Component Component
Structure ratio ture (C) ture (C) ratio (dtex/f) 2.54 cm) (X)
agent(%) 10 min) Example 1 modifiedPE1 PP core/ 65:35 280 90 3.5
1.7 10 A 0.3 10.2 (5%) sheath type HDPE(95%) Example 2 modifiedPE1
PP core/ 65:35 280 90 3.5 1.7 10 B 0.4 7.8 (10%) sheath type
HDPE(90%) Example 3 modifiedPE1 PP core/ 65:35 280 90 3.5 1.7 10 C
0.3 5.5 (15%) sheath type HDPE(85%) Example 4 modifiedPE1 PP
eccentric 65:35 280 90 3.5 1.7 10 D 0.3 3.6 (20%) core/ HDPE(80%)
sheath type Example 5 modifiedPE1 PP core/ 50:50 280 90 3.5 2.0 10
A 0.5 9.2 (10%) sheath type HDPE(90%) Example 6 modifiedPE1 PP
side-by-side 40:60 280 90 3.5 2.0 10 A 0.5 9.7 (10%) type HDPE(90%)
Example 7 modifiedPE1 PP core/ 50:50 280 90 3.5 2.0 10 A 0.6 8.9
(10%) sheath type LLDPE (90%) Example 8 modifiedPE1 PP core/ 50:50
280 90 3.5 1.5 10 B 0.3 8.5 (10%) sheath type co-PP(90%) Example 9
modifiedPE2 PP core/ 50:50 280 90 3.5 3.0 10 B 0.2 8.0 (10%) sheath
type HDPE(90%) Example modifiedPE2 PP eccentric 50:50 280 90 3.5
2.0 10 B 0.2 3.3 10 (50%) core/ HDPE(50%) sheath type Example
modifiedPE2 PP core/ 50:50 280 90 3.5 2.0 10 C 0.8 3.5 11 (50%)
sheath type co-PP(50%) Example modifiedPE3 PP core/ 50:50 280 90
3.5 2.0 10 D 0.5 8.8 12 (10%) sheath type HDPE(90%) Example
modifiedPE4 PP core/ 50:50 280 90 3.5 2.0 10 D 0.6 7.9 13 (10%)
sheath type HDPE(90%) Example modifiedPE5 PP core/ 50:50 280 90 3.5
2.0 10 C 0.3 9.0 14 (10%) sheath type HDPE(90%) Example modifiedPE1
PET core/ 65:35 280 90 3.5 2.0 10 A 1.0 4.2 15 (10%) sheath type
HDPE(90%) Example modifiedPE2 PET eccentric 50:50 280 90 3.5 5.0 10
A 0.7 4.8 16 (10%) core/ HDPE(90%) sheath type Example modifiedPP1
PP core/ 50:50 280 90 3.5 2.0 10 A 0.5 5.0 17 (10%) sheath type
HDPE(90%) Example modifiedPE1 PP core/ 65:35 280 90 3.5 1.7 10 E
0.3 8.7 18 (10%) sheath type HDPE(90%) Example modifiedPE1 PP core/
50:50 280 90 3.5 2.0 10 A 0.6 8.9 19 (10%) sheath type LLDPE (90%)
Example modifiedPE1 PP core/ 50:50 280 90 3.5 2.0 10 A 0.6 8.9 20
(10%) sheath type LLDPE (90%) Example modifiedPE4 PP core/ 50:50
280 90 3.5 2.0 10 D 0.6 7.9 21 (10%) sheath type HDPE(90%) Example
modifiedPE4 PP core/ 50:50 280 90 3.5 2.0 10 D 0.6 7.9 22 (10%)
sheath type HDPE(90%)
[0086]
2 TABLE 2 Fine- Number of Fiber Amount Fiber Sheath/ Spinning
Drawing Draw- ness crimps treating of fiber MFR First Second core
Tempera- Tempera- ing (dtex/ (crimps/ agent treating (g/ Component
Component Structure ratio ture (C) ture (C) ratio f) 2.54 cm) (X)
agent(%) 10 min) Compara- modifiedPE1 PP core/sheath 65:35 280 90
3.5 1.7 10 water -- 26.6 tive (5%) type Example 1 HDPE(95%)
Compara- modifiedPE1 PP core/sheath 65:35 280 90 3.5 1.7 10 alkyl-
0.4 23.5 tive (10%) type phosphate Example 2 HDPE(90%) sodium salt
Compara- modifiedPE1 PP core/sheath 50:50 280 90 3.5 2.0 10 water
-- 27.0 tive (10%) type Example 3 LLDPE (90%) Compara- modifiedPE2
PP eccentric 50:50 280 90 3.5 2.0 10 water -- 19.1 tive (50%)
core/sheath Example 4 HDPE(50%) type Compara- modifiedPE3 PP
core/sheath 50:50 280 90 3.5 2.0 10 water -- 22.2 tive (10%) type
Example 5 HDPE(90%) Compara- modifiedPE4 PP core/sheath 50:50 280
90 3.5 2.0 10 alkyl- 0.6 30.3 tive (10%) type phosphate Example 6
HDPE(90%) sodium salt Compara- modifiedPE1 PET core/sheath 65:35
280 90 3.5 2.0 10 alkyl- 0.5 24.9 tive (10%) type phosphate Example
7 HDPE(90%) sodium salt
[0087] As clearly seen from Tables 1 and 2, the thermoadhesive
conjugate fibers of the invention had lower fiber MFR values
compared to the conventional thermoadhesive conjugate fibers which
were not treated with a fiber treating agent as the essential
condition of the invention. (cf. Example 1: 10.2 g/10 min and
Comparative Example 1: 26.6 g/10 min.) This was due to crosslinking
reaction between the modified polyolefin and multifunctional
compound used according to the invention. The partial reduction in
fiber cross-sectional area resulting from melting and flow off of
the fiber surface caused by heating was thus inhibited, thus
preventing very small (thin) sections of the fiber cross-section
and avoiding strength reduction of the fibers themselves.
[0088] The thermoadhesive conjugate fibers obtained under the
conditions shown in Tables 1 and 2 (corresponding to the examples
and comparative examples) were cut to the prescribed fiber lengths
for the nonwoven fabric production conditions shown in Table 3 (51
mm for carding method, 5 mm for air-laid method), webs were formed
by each method, and then heat treatment was carried out with a
through-air apparatus set to a working temperature of 143.degree.
C. to prepare nonwoven fabrics. The unit weights, specific volumes
and strengths of the obtained nonwoven fabrics are shown in Table
3.
[0089] [Table 3]
3 TABLE 3 unit specific nonwoven Production method weight volume
fabric of nonwoven fabric (g/m.sup.2) (cm.sup.3/g) strength (N/5
cm) Example 1 air-laid method 25 18 50 Example 2 air-laid method 25
18 56 Example 3 air-laid method 25 19 58 Example 4 air-laid method
25 30 61 Example 5 air-laid method 25 23 57 Example 6 air-laid
method 25 25 51 Example 7 carding method 25 35 88 Example 8
air-laid method 25 23 55 Example 9 air-laid method 25 22 58 Example
10 air-laid method 25 29 57 Example 11 air-laid method 25 23 56
Example 12 air-laid method 25 24 53 Example 13 carding method 25 30
76 Example 14 air-laid method 25 23 49 Example 15 air-laid method
25 89 48 Example 16 carding method 25 72 70 Example 17 air-laid
method 25 20 45 Example 18 air-laid method 25 18 46 Comparative
air-laid method 25 18 30 Example 1 Comparative air-laid method 25
18 33 Example 2 Comparative carding method 25 35 55 Example 3
Comparative air-laid method 25 29 26 Example 4 Comparative air-laid
method 25 24 25 Example 5 Comparative carding method 25 30 51
Example 6 Comparative air-laid method 25 89 20 Example 7
[0090] As clearly seen in Table 3, the nonwoven fabrics of the
invention were confirmed to have notably superior nonwoven fabric
strength compared to the conventional nonwoven fabrics wherein the
thermoadhesive conjugate fiber surfaces were not coated with a
fiber treating agent as the essential condition of the invention.
(cf. Example 1: 50 N/5 cm and Comparative Example 1: 30 N/5 cm.)
This was due to crosslinking reaction of the thermoadhesive
conjugate fibers of the invention at the fiber surfaces, as well as
crosslinking reaction at the adhesive point between the fibers
(melt adhesion).
[0091] The thermoadhesive conjugate fibers obtained under the
conditions shown in Tables 1 and 2 (corresponding to the examples
and comparative examples) were cut to the prescribed fiber lengths
for the cellulosic fiber blended nonwoven fabric production
conditions shown in Table 4 (51 mm for carding method, 5 mm for
air-laid method), webs with the cellulosic fiber blend ratios shown
in Table 4 were formed by each method, and then heat treatment was
carried out with a through-air apparatus set to a working
temperature of 143.degree. C. to prepare cellulosic fiber blended
nonwoven fabrics. The unit weights, specific volumes, strengths and
cellulosic fiber (B) losing rates of the obtained cellulosic fiber
blended nonwoven fabrics are shown in Table 4.
[0092] [Table 4]
4 TABLE 4 Production method of cellulosic fiber unit weight
specific volume nonwoven fabric Losing ratio nonwoven fabric
ratio(A %:B %) (g/m.sup.2) (cm.sup.3/g) strength (N/5 cm) of B (%)
Example 1 air-laid method 10:90 80 50 15 1.9 Example 2 air-laid
method 10:90 80 52 16 1.5 Example 3 air-laid method 10:90 80 53 17
0.8 Example 4 air-laid method 10:90 80 52 20 0.3 Example 5 air-laid
method 50:50 80 37 41 0.9 Example 6 air-laid method 50:50 80 35 39
0.7 Example 7 air-laid method 10:90 80 51 13 2.0 Example 8 air-laid
method 30:70 80 43 28 1.2 Example 9 air-laid method 30:70 80 44 27
1.1 Example 10 air-laid method 30:70 80 44 30 2.4 Example 11
air-laid method 10:90 80 50 13 1.8 Example 12 air-laid method 30:70
80 42 28 1.1 Example 13 air-laid method 10:90 80 49 13 2.0 Example
14 air-laid method 10:90 80 53 13 1.0 Example 15 air-laid method
10:90 80 53 12 2.0 Example 16 air-laid method 10:90 80 55 11 2.2
Example 17 air-laid method 10:90 80 48 12 2.3 Example 18 air-laid
method 10:90 80 50 13 2.1 Example 19 carding method 50:50 80 29 48
3.0 Example 20 air-laid method 50:50 80 36 37 1.0 Example 21
carding method 50:50 80 31 46 3.0 Example 22 air-laid method 50:50
80 38 38 0.9 Comparative air-laid method 10:90 80 50 4 5.6 Example
1 Comparative air-laid method 10:90 80 52 5 4.4 Example 2
Comparative air-laid method 10:90 80 51 4 10.1 Example 3
Comparative air-laid method 30:70 80 44 7 6.2 Example 4 Comparative
air-laid method 30:70 80 42 7 4.9 Example 5 Comparative air-laid
method 10:90 80 49 2 9.7 Example 6 Comparative air-laid method
10:90 80 53 2 7.2 Example 7 Notes) A: cut thermoadhesive conjugate
fibers B: cellulosic fibers
[0093] As clearly seen in Table 4, the cellulosic fiber blended
nonwoven fabrics of the invention were confirmed to have notably
superior nonwoven fabric strength (cf. Example 1: 15 N/5 cm and
Comparative Example 1: 4 N/5 cm.) and cellulosic fiber (B) losing
rates (cf. Example 1: 1.9% and Comparative Example 1: 5.6%),
compared to the conventional cellulosic fiber blended nonwoven
fabrics wherein the thermoadhesive conjugate fiber surfaces were
not coated with a fiber treating agent as the essential condition
of the invention. This was due to the reason explained above, and
also to crosslinking reaction between the conjugate fibers and the
cellulosic fibers (B) at the surfaces of the thermoadhesive
conjugate fibers of the invention.
[0094] In addition, the cellulosic fiber blended nonwoven fabrics
obtained by the air-laid method had the thermoadhesive conjugate
fibers (A) and cellulosic fibers (B) more uniformly dispersed and
mixed compared to the cellulosic fiber blended nonwoven fabrics
obtained by the carding method, and therefore the cellulosic fiber
(B) losing rates were more satisfactory (cf. Example 20: 1.0% and
Example 19: 3.0%) and the bulk property was superior (cf. Example
20: 36 cm.sup.3/g and Example 19: 29 cm.sup.3/g). The
thermoadhesive conjugate fibers of the invention may therefore be
considered suitable for obtaining cellulosic fiber blended nonwoven
fabrics by air-laid methods.
Example 23
[0095] The cellulosic fiber blended nonwoven fabric of Example 1 in
Table 4 was cut to a size of 15 cm.times.15 cm and laminated with a
polyethylene film of the same size and subjected to embossing heat
treatment at 125.degree. C. to prepare a floor cleaning wiper.
Comparative Example 8
[0096] The cellulosic fiber blended nonwoven fabric of Comparative
Example 1 in Table 4 was cut to a size of 15 cm.times.15 cm and
laminated with a polyethylene film of the same size and subjected
to embossing heat treatment at 125.degree. C. to prepare a floor
cleaning wiper.
[0097] When the floor cleaning wipers of Example 23 and Comparative
Example 8 were compared, the nonwoven fabric strength of Example 23
was found to be higher than that of Comparative Example 8, and when
used as a wiper it was more resistant to tearing and exhibited
notably improved manageability during wiping. Also, because of its
satisfactory adhesion with the sheet used for lamination, the
manageability was also improved from the standpoint of interlayer
peeling during use of the wiper.
Example 24
[0098] The cellulosic fiber blended nonwoven fabric of Example 1 in
Table 4 was cut to a size of 10 cm.times.25 cm and the entire cut
cellulosic fiber blended nonwoven fabric was folded with a tissue
for use as a paper diaper absorber.
Comparative Example 9
[0099] The cellulosic fiber blended nonwoven fabric of Comparative
Example 1 in Table 4 was cut to a size of 10 cm.times.25 cm and the
entire cut cellulosic fiber blended nonwoven fabric was folded with
a tissue for use as a paper diaper absorber.
[0100] When the paper diaper absorbers of Example 24 and
Comparative Example 9 were compared, the nonwoven fabric strength
of Example 24 was found to be higher than that of Comparative
Example 9, and it thus exhibited more satisfactory shape retention
when used as an absorber, as well as a greater effect of preventing
collapse of the absorber after absorption of water or the like. In
addition, the satisfactory adhesion with the pulp allowed
sufficient water absorption to be exhibited by the absorber.
[0101] The thermoadhesive conjugate fibers of the present invention
are thermoadhesive conjugate fibers which comprise a thermoplastic
resin (I) containing a modified polyolefin with at least one type
of reactive functional group as a first component and a
thermoplastic resin (II) with a higher melting point than the first
component as a second component, having a novel construction
wherein the first component is formed continuously along the length
of at least a portion of the fiber surface, and the fiber surfaces
are coated with a fiber treating agent containing a multifunctional
compound capable of reacting with the reactive functional group in
the modified polyolefin. Heat treatment therefore results in
crosslinking reaction at the fiber surfaces, creating firm adhesion
points when a nonwoven fabric is produced, and yielding
high-strength nonwoven fabrics. In addition, because of their
satisfactory adhesion with other materials and particularly
cellulosic fibers, the resulting cellulosic fiber blended nonwoven
fabrics have almost no peeling or losing of the cellulosic fibers
and exhibit high strength, such that when used as absorbers for
sanitary materials, wipers and the like, very excellent absorption
properties, wiping properties and manageability are exhibited.
* * * * *