EP0089113A2 - Flammhemmende zusammengesetzte Fasern und Verfahren zur Herstellung derselben - Google Patents

Flammhemmende zusammengesetzte Fasern und Verfahren zur Herstellung derselben Download PDF

Info

Publication number
EP0089113A2
EP0089113A2 EP83300640A EP83300640A EP0089113A2 EP 0089113 A2 EP0089113 A2 EP 0089113A2 EP 83300640 A EP83300640 A EP 83300640A EP 83300640 A EP83300640 A EP 83300640A EP 0089113 A2 EP0089113 A2 EP 0089113A2
Authority
EP
European Patent Office
Prior art keywords
fire retardant
composite
melting component
composite fibres
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP83300640A
Other languages
English (en)
French (fr)
Other versions
EP0089113B1 (de
EP0089113A3 (en
Inventor
Shigeru Goi
Taizo Sugihara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JNC Corp
Original Assignee
Chisso Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chisso Corp filed Critical Chisso Corp
Publication of EP0089113A2 publication Critical patent/EP0089113A2/de
Publication of EP0089113A3 publication Critical patent/EP0089113A3/en
Application granted granted Critical
Publication of EP0089113B1 publication Critical patent/EP0089113B1/de
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/06Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/07Addition of substances to the spinning solution or to the melt for making fire- or flame-proof filaments

Definitions

  • This invention relates to fire retardant composite fibres and a process for producing them. More particularly it relates to polyolefin composite fibres comprising two kinds of polyolefin polymers having - different melting points and having the same or different fire retardants in the two components.
  • Polyolefin composite fibres have superior heat adhesive properties and also physical and chemical properties and further are of light weight and cheap; hence they have been used as a fibre material for non-woven fabrics in various applications fields. For example, they are suitable as a material for thin products such as fabric bases, hygienic materials, napkins, paper diapers, and for thick products such as quilting goods, various felts, filters, fibre-shaped products, materials for public works, etc. In general, fire retardant properties have been used indoors for fibre materials.. As a process for making polyolefin fibres fire retardant, there is first a process of adding a fire retardant to raw material polymers, followed by spinning.
  • the present inventors have made various studies on such problems and found that when the higher melting and lower melting components of composite fibres respectively contain a fire retardant having a decomposition temperature higher than the melting points of the respective components by 100°C or more and also having a particle size of 62 microns or less, it is possible to produce superior fire retardant and heat adhesive composite fibres of a small denier having a relatively large amount of the fire retardant blended also with the lower melting component, with a good spinnability.
  • One aspect of the present invention resides in:
  • composite fibres are characterized in that a fire retardant having a decomposition temperature higher than the melting points of the respective components by 100°C or more and also having a particle size of 62 microns or less, is contained in the respective components in an amount of 3 to 15% by weight, and the total of the respective amounts of the fire retardant contained in .
  • the whole of the composite fibres is 5 to 10% by weight.
  • Another aspect of the present invention resides in:
  • Composite fibres of the present invention also have various application fields, and it is particularly preferable for them to be a side by side or a sheath and core type, so that the lower melting component can have a percentage fibre-cross-sectional circumference of 50% or higher, thereby to provide the composite fibres provided with heat adhesive properites by way of the lower melting component.
  • the composite ratio (higher melting component: lower melting component) is preferably in the range of 5:5 to 3:7 in view of the thickness of the lower melting component in the fibre section.
  • the higher melting component is preferably polypropylene or copolymers composed mainly of propylene having a fibre formability.
  • the lower melting component is preferably polyethylene, ethylene-vinyl acetate copolymers, abbreviated to EVA, having a vinyl acetate content of, eg 1 to 10% by weight, their saponified products., blends of polyethylene with EVA or saponified EVA.
  • the respective contents of the fire retardant in the high melting component and the lower melting component of the composite fibres are suitably in the range of 3 to 15% by weight, and the total content of the fire retardant in the whole of the composite fibres is suitably in the range of 5 to 10% by weight. If the contents of the fire retardant are lower than the above ranges, the fire retardant effectiveness is small, and if.the contents exceed the above ranges, the spinnability of the fibres becomes inferor thereby to make their production difficult and degrade their quality.
  • the fire retardant used in the present invention may be suitably selected from known materials.
  • organic halogen compounds are preferable, and concretely preferable examples thereof are decabromodiphenyl oxide (decomposition temperature: 350°C; the temperatures inside the following parentheses likewise indicating decomposition temperature), perchloropentacyclododecane (650°C), ethylenediamine dihydrobromide (355°C), hexabromobenzene (340°C), 2,2-bis[4-(2,3-dibromo- propoxy)-3,5-dibromophenyl]propane (270°C), tris(2,3-dibromopropyl)phosphate (260°C), bis[3,5-dibrom-4-di- bromopropyloxyphenyl]sulfone (280°C), etc.
  • fire retardants are also preferably used in admixture with Sb 2 0 3 in a ratio of retardant to Sb 2 0 3 in a ratio of 1.5:1 to 3:1.
  • the fire retardants used in the present invention have a particle size of 62 microns or less. If the fire retardants contain particles larger than 62 microns, this causes reduction in their productivity or quality, due to, eg, clogging of spinning nozzle, fibre breakage at the time of stretching, forming of rough surface on fibres which lowers their heat adhesive properties.
  • the fire retardants having a particle size of 62 microns or less may be obtained by grading commercially available fire retardants by way of a known method such as a precipitation method, cyclone method, etc, and as a simpler method, by grading them through sieves indicated in JIS Z 8801 (nominal diameter 62 or 53 microns).
  • the fire retardant composite fibres of the present invention may be produced according to a conventional melt-composite-spinning process and the apparatus employed may also be a conventional apparatus.
  • a powdery raw material polymer having a fire retardant mixed is melted and extruded by a melt-extruder and the resulting melt is passed through a temperature- controlled heating zone to heat it to a definite temperature (hereinafter often referred to as spinning temperature).
  • the melting and temperature adjustment of the polymer are carried out in separate passages for each of the commosite components, and the respective composite components each having a definite temperature are fed in a composite ratio into spinning nozzles through the holes of which they are composite-spun.
  • a fire retardant having a decomposition temperature higher than the melting piont of the components by 100°C or more, preferably higher than the spinning temeratures by 40°C or more, thereby to prevent the decomposition and consumption of the fire retardant at the time of spinning.
  • Unstretched filaments obtained by the composite spinning are stretched in an appropriately chosen ratio depending on application fields. Usually the stretching is carried out very often in a stretch ratio of 4 or more.
  • the stretching temperature temperatures in the range of from the softening point of the lower melting component up to a temperature lower than the melting point by 10°C may be employed, but the effect of the extent of the stretching temperature upon the fire retardant properties is little.
  • the process of the present invention it is possible to produce composite fibers containing a large amount of a fire retardant and having a small fineness, with small frequencies of fiber breakage due to clogging of spinning nozzles and exchange of spinning die, in a stabilized manner and over an extremely long term.
  • the fire retardant composite fibers of the present invention are not only provided with fire retardant properties, but also, in spite of a large amount of fire retardant contained therein, have a smooth surface and superior heat adhesive properties.
  • Sb 2 0 3 is regarded as an additive other than fire retardants.
  • JIS method method according to JIS L1091, Al (45° microburner).
  • a polypropylene (PP) having a MFR of 4 (according to JIS K7210, condition 14) and a melting point of 160°C were used.
  • a fire retardant (decabromodiphenyl oxide) having passed through a definite sieve as indicated in the Table shown later, in definite amounts relative to the PE and PP, respectively, as indicated in the Table, and Sb 2 0 3 in 1 / 2 of the respective amounts of the fire retardant were added to the PE and PP, separately.
  • Composite spinning was then carried out in a composite ratio of 1:1, at a spinning temperature on the PE side of 230°C and at that on the PP side of 300°C to obtain unstretched side-by-side composite filaments having percentages fiber-cross-sectional circumference of the._PE component of 78 to 85%. These filaments were stretched to 4 times the original lengths and cut to obtain staple fibers of 18d/f (deniers per filament) x 64 mm, which were then carded to prepare a web of 2 50 g /m 2 .
  • This web was subjected to heat treatment at 140°C for 5 minutes to obtain a sheet of non-woven fabric of 15 mm thick, partially adhered on the PE side.
  • This sheet was allowed to cool in a desicator for 3 - 4 hours, followed by carrying out combustion test according to the above JIS method to measure flame-remaining time (seconds) and carbonized area (cm 2 ). Further, the same sheet of non-woven fabric was subjected to the above combustion test according to the match method. The results of blending of fire retardants, spinning test and combustion tests are shown in the Table.
  • Example 1 and 2 are compared with Comparative examples 1 and 2,and Example 3 is compared with Comparative examples 3 and 4, even if the contents of a fire retardant in the whole of the fibers are the same, if the fire retardant is contained only in an amount less than 3% inside one of the composite components, the fire retardant effectiveness is inferior, and this is remarkable particularly in the evaluation according to the match method. Further, if the fire retardant is contained in an amount exceeding 15% inside one of the composite components, the spinning nozzle life becomes shorter and also the frequency of fiber breakage increases; hence such amount is also undesirable.
  • an ethylene-vinyl acetate copolymer (EVA) having a melting point of 110°C, a content of vinyl acetate component of 5% and a MFR of 25 (according to JIS K7210, condition 2) was used, and as a higher melting component, a polypropylene (PP) having a MFR of 4 was used.
  • EVA ethylene-vinyl acetate copolymer
  • PP polypropylene
  • a blend of perchloropentacyclododecane as a fire retardant to Sb 2 0 3 in a ratio of 2:1 was added in a definite amount to the PP and a blend of bis(3,5-dibrom -4-dibromopropyloxyphenyl)sulfone to Sb 2 0 3 in a ratio of 1.5:1 was added in a definite amount to the EVA, as indicated in the Table.
  • Composite spinning was then carried out in a composite ratio of 1:1 at a temperature of the lower melting component of 200°C and at that of the higher melting component of 280°C to obtain unstretched filaments which were then stretched to 4 times the original length and cut to prepare staple fibers (6d/f ⁇ 64 mm) of sheath and core type composite fibers having a percentage fiber-cross-sectional circumference of the lower melting component of 100%, from which a sheet of non-woven fabric was prepared, followed by subjecting it to a combustion test as in Examples 1 and 2 to evaluate its fire retardant properties. The results are shown in the Table.
  • a polyethylene (MFR: 10) (PE) was used and as a higher melting component, a polypropylene (MFR: 8) (PP) was used-Blends of tris(2,3-dibromopropyl)phosphate, 1,2-dibrom -3-chloropropane or pentadibromomonochloro- cyclohexane as a fire retardant, each in a definite amount, to Sb 2 0 3 in an amount in a ratio of the fire retardant to Sb 2 O 3 of 3:1 were respectively added in a definite amount to PE, while a blend of ethylenediamine dihydrobromide to Sb 2 0 3 in a ratio of 2:1 was added in a definite amount to PP, as indicated in the Table.
  • Composite spinning was then carried out at a temperature on the lower melting component side of 210°C and at that on the higher melting component side of 300°C, in a composite ratio of l:l to obtain unstretched filaments which were then stretched to 4 times the original length and cut to obtain staple fibers of side by side composite fibers (3d/f x64 mm) having a percentage fiber-cross-sectional circumference of the lower melting component of 49 -50%.
  • a sheet of non-woven fabric was prepared from the staple fibers as in Examples 1 and 2 to evaluate the fire retardant properties. The results are shown in the Table.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Multicomponent Fibers (AREA)
  • Nonwoven Fabrics (AREA)
EP83300640A 1982-03-12 1983-02-09 Flammhemmende zusammengesetzte Fasern und Verfahren zur Herstellung derselben Expired EP0089113B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP39167/82 1982-03-12
JP57039167A JPS58156019A (ja) 1982-03-12 1982-03-12 難燃性の複合繊維及びその製造方法

Publications (3)

Publication Number Publication Date
EP0089113A2 true EP0089113A2 (de) 1983-09-21
EP0089113A3 EP0089113A3 (en) 1985-06-05
EP0089113B1 EP0089113B1 (de) 1987-05-13

Family

ID=12545555

Family Applications (1)

Application Number Title Priority Date Filing Date
EP83300640A Expired EP0089113B1 (de) 1982-03-12 1983-02-09 Flammhemmende zusammengesetzte Fasern und Verfahren zur Herstellung derselben

Country Status (7)

Country Link
EP (1) EP0089113B1 (de)
JP (1) JPS58156019A (de)
KR (1) KR880000376B1 (de)
AU (1) AU555246B2 (de)
DE (1) DE3371545D1 (de)
DK (1) DK155803C (de)
FI (1) FI75875C (de)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2268069A (en) * 1992-06-03 1994-01-05 Cindy Michelle Beli Waterfield Disposable nappy
EP1472393A1 (de) * 2001-07-03 2004-11-03 Honeywell International Inc. Dünnmantelfasern hoher festigkeit
US6878650B2 (en) 1999-12-21 2005-04-12 Kimberly-Clark Worldwide, Inc. Fine denier multicomponent fibers
US8281857B2 (en) 2007-12-14 2012-10-09 3M Innovative Properties Company Methods of treating subterranean wells using changeable additives
US8353344B2 (en) 2007-12-14 2013-01-15 3M Innovative Properties Company Fiber aggregate
US8596361B2 (en) 2007-12-14 2013-12-03 3M Innovative Properties Company Proppants and uses thereof
EP2826895A1 (de) * 2013-07-15 2015-01-21 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3289503B2 (ja) 1994-07-08 2002-06-10 チッソ株式会社 難燃性繊維及び不織布

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3658634A (en) * 1970-08-20 1972-04-25 Toray Industries Fire-retardant sheath and core type conjugate fiber

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3658634A (en) * 1970-08-20 1972-04-25 Toray Industries Fire-retardant sheath and core type conjugate fiber

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN, vol. 5, no. 8, (C-39)(680), January 20, 1981 *
PATENTS ABSTRACTS OF JAPAN, Vol.5, No.120 (C-65) (792), August 4, 1981. *
PATENTS ABSTRACTS OF JAPAN, Vol.5, No.8, (C-39) (680), January 20, 1981. *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2268069A (en) * 1992-06-03 1994-01-05 Cindy Michelle Beli Waterfield Disposable nappy
GB2268069B (en) * 1992-06-03 1996-03-06 Cindy Michelle Beli Waterfield Fire retardant disposable nappy
US6878650B2 (en) 1999-12-21 2005-04-12 Kimberly-Clark Worldwide, Inc. Fine denier multicomponent fibers
EP1472393A1 (de) * 2001-07-03 2004-11-03 Honeywell International Inc. Dünnmantelfasern hoher festigkeit
EP1472393A4 (de) * 2001-07-03 2005-08-24 Honeywell Int Inc Dünnmantelfasern hoher festigkeit
US8281857B2 (en) 2007-12-14 2012-10-09 3M Innovative Properties Company Methods of treating subterranean wells using changeable additives
US8353344B2 (en) 2007-12-14 2013-01-15 3M Innovative Properties Company Fiber aggregate
US8596361B2 (en) 2007-12-14 2013-12-03 3M Innovative Properties Company Proppants and uses thereof
EP2826895A1 (de) * 2013-07-15 2015-01-21 Ewald Dörken Ag Bikomponentenfaser zur Herstellung von Spinnvliesen

Also Published As

Publication number Publication date
AU1242483A (en) 1983-09-15
KR840004191A (ko) 1984-10-10
EP0089113B1 (de) 1987-05-13
DK89583A (da) 1983-09-13
KR880000376B1 (ko) 1988-03-20
DK155803C (da) 1989-10-09
EP0089113A3 (en) 1985-06-05
AU555246B2 (en) 1986-09-18
FI75875C (fi) 1988-08-08
FI830779A0 (fi) 1983-03-09
JPS58156019A (ja) 1983-09-16
FI75875B (fi) 1988-04-29
DK155803B (da) 1989-05-16
DK89583D0 (da) 1983-02-25
FI830779L (fi) 1983-09-13
DE3371545D1 (en) 1987-06-19

Similar Documents

Publication Publication Date Title
DE3888859T2 (de) Bikomponentfaser aus Polyolefin und aus dieser Faser hergestellter Vliesstoff.
DE69610856T2 (de) Vliesstoff aus zerblasenem polyäthylen und verfahren zur herstellung
EP0527489B1 (de) Schmelzgeblasener Vliesstoff aus Polyethylenterephthalat und Verfahren zu dessen Herstellung
DE69132180T2 (de) Heiss-verschweissbare Faser mit hoher Festigkeit
EP0364979B1 (de) Weiche, wasserdichte Polyolefinvliesstoffe mit Undurchsichtigkeits-Eigenschaften
DE68918153T2 (de) Schmelzklebende Fasern und deren Anwendung in Vliesstoffen.
AU662011B2 (en) Polyethylene bicomponent fibres
DE69021924T2 (de) Weiche Vliesstoffe aus Fäden.
DE69608577T2 (de) Thermostabiler schalldämmstoff
DE69407677T2 (de) Verbessertes Propylenpolymer-Garn und daraus hergestellter Artikel
DE3650608T2 (de) Zusammensetzung und Verfahren zum Schmelzspinnen von Filamenten
DE69707838T2 (de) Teilchen enthaltende fasern
DE69014777T2 (de) Spaltfasern, damit hergestellte Artikel und Verfahren zu deren Herstellung.
DE69416024T2 (de) Mehrkomponentenfasern mit statistisch verteilten Makrobereichen, ihre Herstellung und daraus hergestellte Vliesstoffe
GB2121423A (en) Hot-melt adhesive fibres
DE2801211A1 (de) Verfahren zur herstellung von tabakfiltern
CA2119477C (en) High strength fine spunbond fiber and fabric
KR960000087B1 (ko) 불투명 특성을 갖는 연수(soft water)투과성 폴리올레핀 부직포
EP0089113B1 (de) Flammhemmende zusammengesetzte Fasern und Verfahren zur Herstellung derselben
KR20110076154A (ko) 위생용품용 폴리올레핀계 단섬유, 부직포, 및 이들의 제조방법
DE69032885T2 (de) Thermisch gebundene fasererzeugnisse mit bikomponentfasern als haftfasern
JPH01246413A (ja) ポリオレフィン系繊維の製造方法
KR20130035503A (ko) 높은 벌키성을 갖는 멜트블로운 부직포 및 그의 제조방법
DE60304890T2 (de) Hohlfaser-Vliesstoff für Weichspülersubstrat
KR101282785B1 (ko) 높은 벌키성을 갖는 멜트블로운 부직포의 제조방법

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19830217

AK Designated contracting states

Designated state(s): DE GB SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): DE GB SE

17Q First examination report despatched

Effective date: 19860220

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE GB SE

REF Corresponds to:

Ref document number: 3371545

Country of ref document: DE

Date of ref document: 19870619

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
EAL Se: european patent in force in sweden

Ref document number: 83300640.6

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19990204

Year of fee payment: 17

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19990211

Year of fee payment: 17

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20000209

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20000210

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20000209

EUG Se: european patent has lapsed

Ref document number: 83300640.6

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20010205

Year of fee payment: 19

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020903