CA1297355C - Cospun 2g-t/66 containing antistat - Google Patents

Cospun 2g-t/66 containing antistat

Info

Publication number
CA1297355C
CA1297355C CA000438274A CA438274A CA1297355C CA 1297355 C CA1297355 C CA 1297355C CA 000438274 A CA000438274 A CA 000438274A CA 438274 A CA438274 A CA 438274A CA 1297355 C CA1297355 C CA 1297355C
Authority
CA
Canada
Prior art keywords
filaments
yarn
cospun
nylon
poly
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.)
Expired - Lifetime
Application number
CA000438274A
Other languages
French (fr)
Inventor
Eugene G. Jones
Donald R. Strachan
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Application granted granted Critical
Publication of CA1297355C publication Critical patent/CA1297355C/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/90Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyamides
    • 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
    • D01F1/09Addition of substances to the spinning solution or to the melt for making electroconductive or anti-static filaments
    • 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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
    • 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
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/62Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/44Yarns or threads characterised by the purpose for which they are designed
    • D02G3/441Yarns or threads with antistatic, conductive or radiation-shielding properties
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2321/00Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D10B2321/02Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
    • D10B2321/021Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polyethylene
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/02Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Woven Fabrics (AREA)
  • Artificial Filaments (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Multicomponent Fibers (AREA)

Abstract

TITLE
COSPUN 2GT/6,6 CONTAINING ANTISTAT
ABSTRACT OF THE DISCLOSURE
Fabrics of reduced static propensity are obtained from cospun yarns comprising a major amount, up to 70 weight percent, of poly(ethylene terephthalate) filaments with the remainder being poly(hexamethylene terephthalamide) filaments containing 3 to 10 weight percent of an N-alkyl substituted polycarbonamide, the filaments having a denier of from 1 to 10.

Description

3 ~ ~

TITLE
COSPUN 2GT/6,6 CONTAINING ANTISTAT
BACKGROUND OF THE INVENTION
l. Field of the Invention This invention relates to antistatic cospun yarn comprising poly(hexamethylene adipamide) filaments and poly(ethylene terephthalate) filaments and to woven and knitted fabrics made therefrom.
2. DescriPtion of the Prior Art The desirability of reducing the electrostatic propensity of synthetic fibers in textile applications is well known. A recent approach to the solution of this problem has been the incorporation of an N-alkyl substituted polycarbonamide into the filaments as described by Alderson U.S. Patent 3,900,676. This patent suggests that such antistatic filaments may form one component of a cospun yarn. It is an object of this invention to provide a cospun yarn containing only a minor proportion of the modified filaments w~ich is capable of achieving the high level of antistatic protection, as shown by reduced garment cling, that is afforded by yarn composed entirely of the modified filaments.
SUMMARY OF_THE INVENTION
This invention provides an antistatic cospun yarn comprising a major amount up to about 70 weight percent of poly(ethylene terephthalate) filaments with the remainder being poly(hexamethylene adipamide) filaments containing 3 to 10 weight percent of an N-alkyl substituted polycarbonamide, the filaments having a denier of from l to 10.
Knitted and woven fabrics of such yarn are also part of this invention.

: ~k . . ~

'3~i DETAILED DESCRIPTION_OF THE INVENTION
The cospun yarn of the invention may be prepared in accordance with the general techniques described in Reese U.S. Patent 3,681,910. Basically, the two fiber-forming polymeric compositions are separately fed to one or more spinning assemblies and extruded to form groups of discrete filaments from each of the polymer compositions in the desired proportions. The filaments are then combined into a single composite yarn and drawn as an integral yarn.
The filaments of the yarn are of textile denier~
preferably from 1 to 10 denier per filament (dpf).
The two fiber-forming polymeric compositions employed in the present invention are poly~ethylene terephthalate) hereinafter 2GT and poly(hexamethylene adipamide) hereinafter nylon 6,6. The nylon 6,6 to be extruded contains from 3 to 10 weight percent of an N-alkyl substituted polycarbonamide as an antis~at modifier. The latter, which is described in more detail below is known to reduce the static propensity of synthetic yarn. The desired yarn desirably contains a major amount of 2GT filaments, preferably about 60% by weight, but no more than 70% by weight.
The remaining filaments in the yarn are constituted ~ 25 by the modified nylon 6~6 filaments. Surprisingly it ; has been found that the static propensity of fabrics of such yarns as shown by cling tests is no greater than that of similar fabrics composed entirely of the modified nylon 6,6 filaments.
The nylon 6,6 filaments contain from about 3 to 10 weight percent of an N-alkyl substituted polycarbonamide modifier in which the tertiary carbonamide groups are an integral part of the polymer molecule. Useful modifiers are those 35 disclosed in Alderson U.S. 3,900,676. The modifier 3~3~

has a molecular weight of at least about 800 to 5000 and is dispersed throughout the filament substantially as a separate phase in the form of discrete elongated conductive particles aligned essentially parallel to the filament axis, all as described in the aforementioned Alderson patent. The elongated conductive particles should have a ratio of their length, L, to average diameter, D, of at least about 100 as taught in said Alderson patent.
In preparing the products of the present invention, the N-alkyl polycarbonamide may be mixed directly with the fiber-forming nylon 6,6 and then immediately spun into filaments. If desired, it may be combined with polymer flake and then spun into filaments. Less reactive N-alkyl polycarbonamides can be introduced into the autoclave during production of the fiber-forming polycarbonamide.
Preferably, the N-alkyl polycarbonamide and fiber~forming nylon 6,6 are mixed in molten condition and immediately spun into filaments.
Useful N-alkyl polycarbonamides are disclosed particularly in column 3 line 7 through line 21 of column 4 of U.S. Patent 3,900,676. In the examples which follow, the modifier employed is the reaction product of a mixture of 80~ N,N'-di-n-butyl hexamethylene diamine and 20% of mono-N-butyl ~ hexamethylene diamine and dodecanedioic acid.
; Stearic acid is employed as a viscosity stabilizer.
The modifier had a melting point less than 0C, a calculated molecular weight o about 2100 and a viscosity of 1100 centistokes at 95C.
The cospun yarns of the examples which follow were prepared using the general procedures described in the aforementioned Reese patent. One filament group of the mixed filament yarn was 2GT

~73~

filaments while the other was nylon 6,6 filaments, the latter having incorporated therein the antistat modifier mentioned above. Two techniques for incorporation of the N-allcyl substituted polycarbonamide are illustrated. In Example I, the modifier was injected into the nylon 6,6 stream shortly beore ex~rusion by injection of the modifier into the screw melter-extruder and mixing before the melt-spinning operation. In Example II, the modifier was combined with the nylon 6,6 in ~he autoclave in the polymerization cycle.
In the examples which follow, cospinning is achieved by separately meter ing 2GT and nylon 6,6 containing modifier to two separate inlet ports of a melt spinning assembly designed to accommodate the two streams and keep them separate. The polymers are discharged in a conventional manner through a spinneret. The two groups of filaments merge and are then drawn and wound up in a package. Details are given in the examples~
TEST PROCEDURES
Relative_viscosity, RV, of 2G~ as used in the following examples is the ratio of the viscosity of a 4.75 weight percent solution of 2GT in hexafluoroisopropanol to the viscosity of the hexafluoroisopropanol per se, measured in the same units at 25C. The RV of nylon 6,6 is measured as described in U.S. 3,681,910 at column 3, lines 25-30.
Sail Test - this test is performed as described in U.S. 3,900,676 at column 16, lines 11-36.
Keithley Log R - this test is performed as described in AAATC 76-1978 p. 233.
Skein_Loq R - this test is similar to the yarn log R test in U.S. 3,900,676 except that for Skein Log R, sufficient revolutions were wound to ~ ' .

:~2~ 3~ ~
.

make a skein with a cross-section of 720,000 denier.
The skein i5 scoured, drled and conditioned at 20~
relative humidity ~or 24 hours. The skein is cut and clamped without spreading between electrodes 2.0 inches apart so that 360,000 denier is between the electrodes. The resistance is measured at 20~
relative humidity with a megohmeter under a potential of 210 volts.
EXAMPLE I
Cospun yarns of trilobal 2GT filaments ~60 by weightj and trilobal nylon 6,6 filaments (40~ by weight) containing antistat modifier were prepared from nylon 6,6 (42 R.V. with 0.02% TiO2) containing 4.6% by weight of modifier and from 2GT (22 R.V. with 0.1~ TiO2). The polymers were melt spun at 291C
through a single spinneret into a yarn (6 filaments of each polymer) in which the nylon 6,6 filaments had an R.V. o~ 47.7 and the 2GT filaments an R.V~ of 21.5. The extruded filaments were air-quenched.
Finish was applied and the filament streams were conver~ed to a feed roll operating at 1564 ypm surface speed and then passed through a steam jet at 200C to a draw roll operating at a surface speed of 3674 ypm for a draw ratio of 2.35. The drawn yarn was annealed at 138C in a hot chest kesidence time about 0O2 sec.). The drawn yarn was passed through an interlace jet at 55 psig air, treated with a second finish and wound up at 3681 ypm at a tension of 7 grams. The yarn denier was 40, percent elongation was 35.4, tenacity was 3.5 gpd. The nylon 6,6 filaments had a denier of 2.7 while the 2GT
filaments had a denier of 4Ø The antistatic performance of skeins and warp knit fabrics from the yarns is reported as Item 1 on Table I below.

73~

EXAMPLE II
A process similar to that used in Example I
was performed except that the polymers used were nylon 6,6 ~32 R.V. wi~h 0.02~ TiO2) containing 5.25% by weight of modiEier and 2GT (22 R~V. with 0.1~ TiO2). The resulting yarn was made up of nylon 6,6 filaments (40~ by weight) of 39.5 R.V. and 2GT filaments (60% by weight) of 21.2 R.V. The yarn denier was 40, percent elonga~ion was 42.5, and tenacity was 3.5 gpd. The antistatic performance of the yarn and the performance of warp knit fabrics of such yarns is reported on Table I as Item 2.
Item 3 of Table I represents a cospun trilobal control yarn containing no antistat modifier, but is otherwise similar to Items 1 and 2.
Items 4, 5 and 6 are commercial warp knit fabrics from 40 denier yarn. Item 4 is a trilobal nylon antistatic 13-filament yarn. Item 5 is a quadralobal nylon antistatic 20-filament yarn and 20 Item 6 is a round nylon 13-filament yarn containing no antistat. Items ~ and 5 contain the same modifier as used for Item 1 and at a concentration of 5.25%.
Item 7 and 8 represent experiments performed to compare results obtained from nylon 6,6 yarns in which modifier 5.25% concentration was added to 100%
of the filaments (Item 7~ and nylon 6,6 yarns in which modifier was added at 5.25~ concentration to only 50% of the filaments (Item 8). In each case the same modifier was used.

.~ . . .

f ~

_A LE I
SAIL TEST
PRIMARY
DECLING ANTISTATIC PERFORMANCE
SKEIN MINS. KEITHLEY LOG "_"
5 ITEM LOG R 5 "C" WASH AS REC'D. _ C" WAS~
_ 12~8 3~8 14~7 14~4 2 12~9 3~7 1~L~6 14~6 3 ;~14~0* 9~2 17~4 17~0 4 12~9 ~~ 1~Lo6 14~4 10 5 12~5 5~2 13~0 13~7 6 ~14~0* ~~ 17~1 17~4 7 12 ~ 95 8 13~25 _ * The value reported was the upper limit of the instrument capability.

. , .

Claims (2)

1. An antistatic cospun yarn comprising a major amount up to about 70 weight percent of Poly(ethylene terephthalate) filaments, the remainder being poly(hexamethylene adipamide) filaments containing 3 to 10 weight percent of an N-alkyl substituted polycarbonamide, the filaments having a denier of from 1 to 10.
2. The yarn of claim 1 comprising about 60 weight percent 10 of poly(ethylene terephthalate) filaments.
CA000438274A 1982-10-04 1983-10-04 Cospun 2g-t/66 containing antistat Expired - Lifetime CA1297355C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US43244382A 1982-10-04 1982-10-04
US432,443 1982-10-04

Publications (1)

Publication Number Publication Date
CA1297355C true CA1297355C (en) 1992-03-17

Family

ID=23716180

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000438274A Expired - Lifetime CA1297355C (en) 1982-10-04 1983-10-04 Cospun 2g-t/66 containing antistat

Country Status (12)

Country Link
EP (1) EP0114933B1 (en)
JP (1) JPS5988912A (en)
KR (1) KR910005543B1 (en)
AR (1) AR231552A1 (en)
AU (1) AU557233B2 (en)
BR (1) BR8305392A (en)
CA (1) CA1297355C (en)
DE (1) DE3380266D1 (en)
DK (1) DK159828C (en)
GR (1) GR79697B (en)
IE (1) IE54756B1 (en)
MX (1) MX157144A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0250664B1 (en) * 1986-06-30 1990-10-03 E.I. Du Pont De Nemours And Company Process for combining and codrawing antistatic filaments with undrawn nylon filaments
US4668453A (en) * 1985-02-15 1987-05-26 E. I. Du Pont De Nemours And Company Cospinning process
JPH07103489B2 (en) * 1986-07-01 1995-11-08 イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− Method for combining and co-stretching antistatic filaments and non-stretched nylon filaments

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1442735A (en) * 1964-09-25 1966-06-17 American Cyanamid Co New blend of textile fibers with improved anti-static properties
US3987613A (en) * 1965-07-29 1976-10-26 Burlington Industries, Inc. Process for preparing textiles without static charge accumulation and resulting product
US3900676A (en) * 1967-09-19 1975-08-19 Du Pont Antistatic filaments
JPS5319071B2 (en) * 1971-10-18 1978-06-19
US3803453A (en) * 1972-07-21 1974-04-09 Du Pont Synthetic filament having antistatic properties
JPS5857527B2 (en) * 1974-02-18 1983-12-20 東レ株式会社 Method for producing antistatic thermoplastic synthetic fiber
US4025595A (en) * 1975-10-15 1977-05-24 E. I. Du Pont De Nemours And Company Process for preparing mixed filament yarns
JPS55137221A (en) * 1979-04-16 1980-10-25 Teijin Ltd Antistatic composite filament and its preparation

Also Published As

Publication number Publication date
IE832318L (en) 1984-04-04
DE3380266D1 (en) 1989-08-31
EP0114933A2 (en) 1984-08-08
EP0114933B1 (en) 1989-07-26
KR840006378A (en) 1984-11-29
JPS5988912A (en) 1984-05-23
KR910005543B1 (en) 1991-07-31
IE54756B1 (en) 1990-01-31
AU1982083A (en) 1984-04-12
DK159828B (en) 1990-12-10
EP0114933A3 (en) 1986-03-12
DK456083D0 (en) 1983-10-03
MX157144A (en) 1988-10-28
DK159828C (en) 1991-05-06
AR231552A1 (en) 1984-12-28
GR79697B (en) 1984-10-31
AU557233B2 (en) 1986-12-11
BR8305392A (en) 1984-05-15
DK456083A (en) 1984-04-05

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