FLAME RESISTANT BLENDS

Information

  • Patent Application
  • 20130212790
  • Publication Number
    20130212790
  • Date Filed
    March 15, 2013
    11 years ago
  • Date Published
    August 22, 2013
    11 years ago
Abstract
A flame retardant fibre blend comprising: a flame retardant fibre blend comprising: 40% to 60% by weight of a modacrylic; 5% to 25% by weight of a natural cellulosic material; and 20% to 40% by weight of a FR viscose based material; wherein any remaining weight % is made up of any one or a combination of the modacrylic, cellulosic or FR viscose or of nylon in range trace to 7% or para-aramid fibre in the range trace to 7%. The fibre blend is particularly suitable for the manufacture of a ‘universal’ fabric configured to be resistant to flame, flash fire hazard, electric discharge and molten metal hazards.
Description

The present invention relates to a flame resistant fibre blend and in particular, although not exclusively, to yarns, fabrics, garments, woven, knitted, and non-woven products prepared from a flame resistant fibre blend.


Flame Resistant (FR) materials are employed in many textile applications. In particular, FR materials are used as barrier layers to protect more flammable internal components such as inner stuffing within furniture including mattresses, sofas and the like. FR materials are also used to make FR clothing used in specific industrial applications and the military.


First generation fire resistant materials, particularly for the construction of garments to be worn, were based on natural fibres, including in particular wool and cotton. The flame retardant functionality was provided by chemically treating the natural yarns with phosphorous based flame retardant chemicals. The resultant garments, whilst being resistant to flames were however disadvantageous for a number of reasons. In particular, these early FR garments were uncomfortable to wear for reasonable periods as they were typically heavy with the wearer becoming increasingly hot. More recently, synthetic FR blends have been developed with a view to providing lighter more breathable garments so as to increase comfort.


US 2008/0145543 discloses a high performance FR textile fabric for use in producing close fitting garments, such as undergarments, in direct contact with the skin. The fabric is formed from yarns of rayon filaments, and a cured phosphorous-based flame retardant compound is affixed to the filaments and imparts further flame retardant properties to the fabric.


US 2005/0204718 discloses a blended yarn designed to provide arc and flame protective properties. The yarn is manufactured from 40% to 70% by weigh of a modacrylic, 5% to 20% by weight of p-aramid and 10% to 40% by weight of m-aramid. The entirely synthetic material is designed to achieve a tensile strength sufficient to be resistant to ‘break-open’ when exposed to an electric arc.


WO 2008/027454 discloses flame resistant fabrics comprising a blend of a synthetic cellulosic and a FR modacrylic. Garments produced from the fibres are designed to be resistant to electric arc flash and flames.


However, whilst these more recent synthetic FR textiles perform better than the earlier natural fibre based garments there are a number of disadvantages. Firstly, entirely synthetic FR garments are expensive for a number of reasons. The component fibres are typically only available from specialist manufacturers resulting in limited availability. Secondly, the manufacture of these component fibres is complex, requiring a variety of chemical processing steps. Thirdly, FR textiles made entirely from synthetic fibres are typically uncomfortable for the wearer due, in part, to their poor softness and breathability characteristics.


There is therefore a need for a flame retardant fibre blend that may be conveniently and efficiently mass produced for the manufacture of FR garments that satisfy the required national and/or international safety standards whilst being comfortable for the wearer.


Accordingly, the inventors provide a fibre blend that is designed to be breathable, soft and provide moisture management characteristics. The present fibre blend is also configured to be multipurpose being suitable for use as a safety garment that offers a protective function within a variety of very different hazardous environments. Utilising natural materials further provides for a cost effective solution to the problem of increasing the FR of a textile.


For example, fabrics manufactured from the present fibre blend are configured to satisfy a variety of different safety standards including in particular, flame retardance protection against radiant and convective heat; electric arc; contact heat and protection against the effects of a hydrocarbon flash fire.


The present fibre blend comprises both synthetic and natural fibres. In particular, a natural cellulosic material is employed to provide a garment that is comfortable for the wearer due, in part, to the breathability and softness. The moisture management characteristics of the resulting textiles are also enhanced due primarily to the ‘wicking’ characteristics resultant from the synergistic combination of the natural and synthetic materials.


The present blend is specifically configured to be blended and spun to form a yarn having a composite structure formed from the fibre blend.


According to a first aspect of the present invention there is provided a flame retardant yarn having a composite structure formed from a collection of fibres twisted together, the fibres comprising a blend of:

    • 40% to 60% by weight of a modacrylic;
    • 5% to 25% by weight of a natural cellulosic material; and
    • 20% to 40% by weight of a FR viscose based material.
    • Optionally, any remaining weight % is made up of any one or a combination of the modacrylic, cellulosic or FR viscose, a polyamide in the range trace to 7% by weight or para-aramid fibre in the range trace to 7% by weight.


The term modacrylic fibre refers to a modified version of acrylonitrile which is resultant from the copolymerisation of acrylonitrile with another compound. The copolymer may comprise 30% to 70% by weight of acrylonitrile and 70% to 30% by weight of a halogen-containing vinyl monomer. The halogen-containing vinyl monomer is preferably at least one monomer selected from vinyl chloride or vinylidene chloride.


Preferably, the modacrylic fibres are copolymers of acrylonitrile combined with vinylidene chloride, the copolymer further comprising at least one type of antimony oxide for improved fire retardancy. In particular, antimony trioxide and/or pentoxide may be used to dope the resultant copolymer. Accordingly, the flame retardant, physical and mechanical properties of the fibre blend may be tailored by, in particular, variation of the type and quantity of the antimony oxide added.


According to specific implementations, the modacrylic fibre of the present invention comprises the fibres disclosed in U.S. Pat. No. 3,193,602; U.S. Pat. No. 3,748,302; U.S. Pat. No. 5,208,105 and U.S. Pat. No. 5,506,042, the contents of which are incorporated by reference herein.


The preferred modacrylic fibres of the present invention are fibres based on Kanecaron™ (available from Kaneka Corporation, Kanecaron Division, 3-2-4, Nakanoshima, Kita-ku, Osaka 530-8288, Japan). Reference to Kanecaron™ includes Kanekaron™ and Kanekalon™.


More preferably, the present fibre blend may comprise any one or a combination of different grades of Protex™ selected from: Protex™ W; Protex™ M; Protex™ T; Protex and/or other modacrylic FR materials falling within the Protex™ family and available from Kaneka.


Preferably, the modacrylic comprises Protex Q™. Optionally, the modacrylic may comprise Sevel™ (available from Fushun Huifu Fire Resistant Fibre Co Limited, No 54, West Section Anshan Road, Fushun City, Conn.-113001 Lianong, China). Optionally, the modacrylic may comprise Tairylon™ (available from Formosa Chemical & Fibre Corporation, 201 Tung Hwan Road, Teipei, Taiwan, R.O.C).


The FR viscose may be sourced from a plurality of different manufacturers to suit the FR, physical and mechanical performance as required. In particular, and optionally, the FR viscose comprises Lenzing FR™ (available from Lenzing Fibres Inc, Aktiengesellschaft, 4860 Lenzing, Austria). Optionally, the FR viscose may be sourced from Shandong Helon Co. Ltd, No 555, Hai Long Road, Hanging District, Wei Fang, SDG 261100, China (herein referred to as Helon FR).


Preferably, the natural cellulosic material comprises any one or a combination of the following set of: Natural Cotton; Bamboo; Linen; and/or Jute. Reference to ‘natural cellulosic’ refers to a cellulosic material that has not been pre-treated so as to change the chemical, physical or mechanical properties including in particular enhancement of FR. This term also refers to a material available from a biological source such as a plant or shrub. The term includes such natural materials that have undergone minimal processing such that the resultant materials cannot be categorised as synthetic or ‘man-made’.


Optionally, the blend may further comprise nylon in the amount trace to 7% by weight or more preferably trace to 5% by weight.


Optionally, the blend may further comprise a para-aramid material in the amount trace to 7% by weight or more preferably trace to 5% by weight.


Optionally, the blend may further comprise an antistatic material and in particular a carbon based antistatic material in the amount trace to 5% by weight. The carbon or non-carbon based antistatic material may be sourced from a plurality of different manufacturers to satisfy the desired physical and mechanical properties as required. However and preferably, the antistatic material comprises any one or a combination of the following set of: Beltron™ (available from KB Seiren Limited, 14-15F, Umeda Daibiru Building, 3-3-10, Umeda, Kita-ku, Osaka, 530-0001 Japan); Negastat™ (available from William Barnet & Son, LLC, 1300 Hayn Street, P.O. Box 131 Arcadia, S.C., 29320, United States of America); antistatic material and fibres available from Jarden, US; and/or Bekinox™ (available from Bekaert, President Kennedypark 18, B-8500 Kortrijk, Belgium).


Preferably, the fibre blend comprises 40% to 55% by weight of the modacrylic; 10% to 20% by weight of the natural cellulosic material; and 25% to 35% by weight of the FR viscose based material.


More preferably, the fibre blend comprises: 45% to 55% by weight of Protex™; 10% to 20% by weight of natural cotton; 25% to 35% by weight of FR viscose; trace to 7% by weight nylon; and trace to 5% by weight of a carbon based antistatic material.


More preferably, the fibre blend comprises: 45% to 55% by weight of Protex™ T; 10% to 20% by weight of natural cotton; 25% to 35% by weight of FR viscose; trace to 7% by weight para-aramid; and trace to 5% by weight of a carbon based antistatic material. According to a further aspect of a present invention there is provided a fabric comprising a fibre blend as disclosed herein. According to a further aspect of the present invention there is provided a garment comprising a fabric made from the fibre blend as disclosed herein.


The present blend of textile fibres is suitable to form yarns to construct fabrics and/or garments that are considered fire and flame retardant such that garments formed from the present yarns may be worn in conditions where there is any threat of heat or flame trauma. The present blend is further advantageous by including natural fibre components to facilitate a degree of comfort to the wearer which cannot be achieved with blends of wholly synthetic component. The present fabrics and garments comprise thermostable elements or components to ensure compliance with relevant health and safety requirements whilst being comfortable and lightweight but achieving a high degree of protection against heat and flame.


The present blend may be presented in blend form, as yarns formed from staple fibres, filamentous yarns, filaments including monofilaments and multifilaments. Fabrics according to the present invention are constructed via the use of the present blend or a union of the present blended fibres in woven, non-woven, or knitted form.


In one aspect, the present invention comprises a knitted fabric comprising a fibre blend as described herein further comprising an antistatic fibre or fibres as a fibre yarn or filament wherein the antistatic fibre is included in the range trace to 10% by weight. According to further aspect, the present invention may comprise a woven fabric formed from the present fibres in a blend or union optionally further including addition of an antistatic fibre or fibres included in the range trace to 10% by weight.


Advantageously, the present fabrics comprise thermostable yarns or filaments or a combination of yarns and filaments in which yarns or filaments of a first type are interlaid, interlinked, interwoven or looped with yarns or filaments of a second type to create a blended composite fabric structure.


The thermostable component may comprise anyone or a combination of the following set of:

    • meta-aramid (e.g., NOMEX by E.I. Du Pont de Nemours and Co.)
    • para-aramid (e.g., KEVLAR by E.I. Du Pont de Nemours and Co. and TWARON by Teijin and FENYLENE ST Russian State Complex))
    • polybenzimidazole (e.g., PBI™ Hoechst Celanese Acetate LLC)
    • p-phenylene benzobisoxazole (PBO) (e.g., ZYLON by Toyobo Co.)
    • polysulphonamide (PSA) (e.g., TANLON by Shanghai Tanlon Company)
    • a polyamide-imide (PAI) (e.g., KERMEL by Rhone-Poulenc)


The thermostable fibres may comprise any one or a combination of the following set of: melamines, polyimides, polyamideimides, partially oxidized polyacrylonitriles, novoloids, poly (p-phenylen benzothiazoles), polyphenylene sulphides, polyethyl- or polydiethyl-ketones, polyketones, polyetherimides, and combinations thereof.


Advantageously, the thermostable component of the fabric as identified herein, is used to form a ‘construct’ reinforcement component of the fabric that provides structural integrity to the fabric during and following exposure to heat and flame Preferably, the thermostable component is included as a minority component within the fabric with the majority component being formed from the yarns or filaments of the present fibre blend comprising a modacrylic, cellulosic and FR viscose. Reference within the specification to minority and majority component encompass volume and weight percentage relative amounts of the first yarn, the second yarn or filament type and the combined volume or weight percentage of the first and second yarn or filament types.


According to a further aspect of the present invention there is provided a flame retardant fibre blend comprising:

    • 40% to 60% by weight of a modacrylic;
    • 5% to 25% by weight of a naturally occurring cellulosic material; and
    • 20% to 40% by weight of a FR viscose based material; and
    • 5 to 20% by weight of a thermostable fibre that exhibits no appreciable decrease in mechanical strength after exposure to heat or flame in excess of 500° C.


Optionally, the blend comprises 5 to 20% of a polyamide.


Optionally, the thermostable element is a blend and comprises any one or a combination of:

    • 5 to 95% by weight of a thermostable fibre being anyone or a combination of the following set of: meta-aramid, para-aramid, polybenzimidazole, p-phenylene benzobisoxazole (PBO), polysulphonamide (PSA), a polyamide-imide (PAI), melamine, carbon fibre, glass fibre;
    • 30 to 70% by weight of a modacrylic;
    • 30 to 70% by weight of a FR viscose based material; and
    • 5 to 20% by weight of a naturally occurring cellulose material;
    • trace to 5% of nylon.


Optionally, the majority component fibre blend and/or the minority thermostable fibre blend includes an antistatic fibre (as described herein) included in the range trace to 10% by weight.


According to a further aspect of the present invention there is provided a flame retardant fabric having a composite structure comprising;

    • a first yarn forming a majority component of the fabric, the first type having a composition comprising:
      • 40% to 60% by weight of a modacrylic;
      • 5% to 25% by weight of a naturally occurring cellulosic material; and
      • 20% to 40% by weight of a FR viscose based material; trace to 5% of nylon or para-aramid; and
    • a second yarn and/or filament type forming a minority component of the fabric, the second yarn and/or filament type comprising a thermostable fibre that exhibits no appreciable decrease in mechanical strength after exposure to heat or flame in excess of 500° C.


Preferably, the fabric comprises a woven structure wherein the majority of the warps and wefts of the weave comprise the first yarn type; and wherein the second yarn and/or filament type is interwoven as warps and wefts at spaced apart intervals amongst the warps and wefts formed from the first yarn type.


Preferably, the second yarn and/or filament type is interwoven with the first yarn type at a regular spacing in the range 5 to 15 ends and 5 to 15 picks. More preferably, the second yarn and/or filament type is interwoven with the first yarn type at a regular spacing in 10 ends and 10 picks.


The second yarn or filament type may comprise a single or two-ply structure. Where the second yarn and/or filament type comprises a two-ply structure, a first strand may comprise a yarn or filament formed from 100% by weight of the thermostable component and the second strand may comprise a yarn formed from the present blend. Optionally, the first strand may comprise 50:50 of the thermostable component and a modacrylic and the second strand may comprise 50:50 of the thermostable component and a modacrylic. Preferably, the first strand of the two-ply construct comprises 100% by weight para-aramid with the second strand comprising 100% by weight of the present blend.


Optionally, the second yarn or filament type may comprise a core spun construction wherein the central core strand comprises 100% para-aramid and the surrounding coil spun strand (sheath) comprises a yarn or filament formed from the present blend.


The second yarn or filament type is preferably interwoven with the first yarn type at regular spaced apart intervals. In particular, the second yarn or filament type may be included at a space in between every 5 to 15 warp and wefts formed from a yarn or filament of the first type. Accordingly, the second yarn or filament type is included within the fabric as a grid or mesh having warps and wefts included at every 10 ends and 10 picks of the fabrics in which the first yarn is the majority component. This second yarn or filament type therefore provides a ‘construct’ or reinforcement component to the fabric that maintains its physical integrity and warp and weft structure during and following exposure to flame and heat in excess of 500° C.


Reference within the specification to ‘a thermostable fibre that exhibits no appreciable decrease in mechanical strength’ encompasses a yarn or filament that retains the majority of its structure during and post exposure to heat in excess of 500° C. That is, where the thermostable yarn or filament is included as a component within a fabric in the form of a weft and warp, during and after exposure to heat in excess of 500° C., the thermostable warp and weft components of the fabric persist and have not perished to form a residual part of the fabric in the form of a grid or mesh that provides structural support for the majority component of the fabric that may have been charred, burnt, scorched, damaged and in some way degraded by the exposure to heat in excess of 500° C.


The present fibre blend is designed specifically for the manufacture of safety textiles being resistant to heat including extreme heat associated with molten metals, electric discharge and flames. The inventors provide a fibre blend and in particular a woven, non-woven, including a knitted fabric, that satisfies a number of different national performance test standards including in particular:


EN ISO 11611: 2007: Clause 6.1—tensile strength; Clause 6.2—tear strength; Clause 6.5—dimensional change; Clause 6.7—flame spread procedure A (surface ignition) and B (edge ignition); Clause 6.10—electrical resistance.


EN ISO 11612: 2008: Clause 7.4—molten aluminium splash; Clause 7.5—molten iron splash; Clause 7.6—contact heat.


NFPA 2112:2012: Section 7.1.1 Heat Transfer Performance (HTP; 7.1.2 flame resistance; 7.1.3 thermal shrinkage; 7.1.4 heat resistance; 7.1.5 predicted body-burn.


A protective fabric, particularly formed as a garment, capable of satisfying the above performance test requirements and based on a natural cellulosic material would provide significant advantages over existing FR fabrics. For example, the present safety fabric satisfies all of the above requirements and is capable of being characterised as a ‘universal’ safety fabric suitable for use in a variety of different hazardous environments as may be required by personnel working in for example, the military, rescue/emergency services and the metal manufacturing, utilities (oil, gas and electric), petrochemical and heavy industries.


The inventors identified the following criteria as being particularly important in the development of a universal heat resistant fibre


(a) required to pass the FR requirements of ISO11612 and associated Standards namely to withstand both face ignition source (as the previous Standard EN531) AND bottom-edge ignition source (as specifically required in the new replacement Standard ISO11612 and associated standards);


(b) required to have minimum tensile and tear strength properties of at least the minima specified in ISO11612 and EN11611


(c) required to achieve the requirements of Oekotex (Okotex) 100 “Standard”. Oekotex is a voluntary, non-Statutory, requirement for measurement of hazardous substances as defined only by the Oekotex organisation but may be used as a bench-mark by some end users. One of the qualifying criteria concerns the measurement of extractable antimony, which is used in the flame-retardant technology inherent to the modacrylic family of fibres.


Modacrylic fibres based on Protex™ W, Protex™ M, Protex™ Q and Protex™ T were identified as suitable components for the present fibre blend due to their FR grading. However, Protex™ T is generally acknowledged to be less ‘protective’ when employed in the manufacture of a garment due to its expected performance with respect to ‘charring’protection (associated with barrier formation within the textile to prevent flame penetration).


The present fibre blend is advantageously suited to form a blended spun yarn


As will be appreciated, the present blend may be used to form a yarn via a process of mixing, carding, drawing, roving, spinning, twisting and winding as will be appreciated by those skilled in the art. In particular, the present fibre blend is specifically non-slickened or siliconised such that the staple fibres may be spun and/or twisted together to form the composite yarn structure wherein the fibres are held together via frictional contact being facilitated by the spinning and twisting construction as described above.


To illustrate the present invention, the following examples are provided. Test results, for the above criteria are also presented and confirm the advantages of the subject invention and its suitability for use as a component fibre of a protective textile and garment exhibiting degradation resistance to a variety of different hazardous environmental conditions involving significant elevated temperatures.







EXAMPLE 1

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ M; 30% Helon FR viscose; 15% cotton and 5% nylon.


EXAMPLE 2

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ W; 30% Helon FR viscose; 15% cotton and 5% nylon.


EXAMPLE 3

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ T; 30% Helon FR viscose; 15% cotton and 5% nylon.


EXAMPLE 4

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ M; 30% Lenzing™ FR viscose; 15% cotton and 5% nylon.


EXAMPLE 5

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ W; 30% Lenzing™ FR viscose; 15% cotton and 5% nylon.


EXAMPLE 6

A fibre blend was ring spun on a cotton system to 40/2 NM. The fabric was woven to a twill construction at approximately 360 gsm. The fibre blend comprised 50% Protex™ T; 30% Lenzing™ FR viscose; 15% cotton and 5% nylon.


Performance testing was undertaken for the fibre blends of examples 3 and 6 and the results are presented in tables 1 to 6 below.


Test Results
EXAMPLE 3

Tables 1 to 3 detail the experimental performance test results for the blend formulation of example 3 according to the identified performance criteria of each of the two standards EN ISO 11611: 2007; EN ISO 11612: 2008


Performance Test—EN ISO 11611: 2007

Standard: Clause 6.1—tensile strength; Clause 6.2—tear strength; Clause 6.5—dimensional change; Clause 6.7—flame spread procedure A (surface ignition) and B (edge ignition); Clause 6.10—electrical resistance.


Pre-treatment: for 6.1, 6.2, 6.5 and 6.10 tests were made after 5 washing cycles in accordance with ISO 6330: 2000. Procedure 6A at 40° C. drying procedure E: tumble dry. The tumble drying was carried out after the completion of each wash. For 6.7 tests were made in the as received condition.









TABLE 1







Standard EN ISO 11611:2007 - Test results for the blend of example 3.













ISO 11611 Requirement &

PASS/Fail


Clause
Test Method
Performance Levels
Results
or Class















6.1***
ISO
Class 1 & 2
Warp
 980 N
LIKELY TO


Tensile strength
13934-1:1999
Min. of 400 N in both the warp
Weft
 930 N
MEET




and weft directions


CLASS 1 &







CLASS 2


6.2***
ISO
Class 1 & 2
Torn across warp
32.1 N
LIKELY TO


Tear strength
13934-1:2000
Min. of 20 N in both the warp and
Torn across weft
29.7 N
MEET




weft directions


CLASS 1 &







CLASS 2


6.5
ISO 5077
Class 1 & 2
Warp
Weft
FAIL


Dimensional

Max ± 3%
−7.0%
−4.5%











change

(−indicates shrinkage)
(−indicates shrinkage)



6.7****
ISO 15025:2000
Class 1 & 2
Procedures A & B
LIKELY TO


Limited

No flaming to top or side edge
No flaming to top or side edge
MEET


flame spread

No hole formation (A only)
No hole formation
CLASS 1 &


(procedures A & B)

No flaming or molten debris
No flaming or molten debris
CLASS 2




Mean afterflame ≦2 s
No afterflame




Mean afterglow ≦2 s
No afterglow


6.10
EN 1149-2:1997
Class 1 & 2
Resistance = 5.2 × 106
CLASS 1 &


Electrical Resistance*****

Electrical resistance greater than

CLASS 2




105 Ohms





*** test made on two warpway and weftway specimens only


****test made on one warpway and weftway specimen only and without pre-treatment


*****sub contracted test made by STFI






Performance Test—EN ISO 11612: 2008

Standard: Clause 7.4—molten aluminium splash (D); Clause 7.5—molten iron splash (E); Clause 7.6—contact heat (F).


Pre-treatment: tests were made after 5 washing cycles in accordance with ISO 6330: 2000. Procedure 6A at 40° C. drying procedure E: tumble try. The tumble drying was carried out after the completion of each wash.









TABLE 2







Standard EN ISO 11612: 2008 - Test results for the blend of example 3.











ISO 11612 Requirement &





Performance Levels

PASS/Fail













Clause
Test Method
Performance levels
Min
Max
Results
or Class
















Molten AL splash (g)
Spec
Poured(g)
Skin stimulant
















7.4
ISO 9185
D1
100
<200
1
203
Damaged
LEVEL D1


Molten

D2
200
<350
2
102
Undamaged


Aluminium

D3
350

3
105
Undamaged


splash (D)




4
107
Undamaged







5
108
Undamaged













Molten Iron splash (g)
Spec
Poured(g)
Skin stimulant
















7.5
ISO 9185
E1
60
<120
1
200
Undamaged
LEVEL E3


Molten Iron

E2
120
<200
2
202
Undamaged


Splash (E)

E3
200

3
203
Undamaged







4
202
Undamaged













Threshold time (s)


















7.6
ISO 12127:
F1
5.0
<10.0
Specimen 1
5.2
LEVEL F1


Contact
1996 at 250° C.
F2
10.0
<15.0
Specimen 2
5.2


Heat (F)**

F3
15.0


Specimen 3


5.1








Result based
5.1







on lowest





**sub contracted test made by UKAS accredited laboratory






Test Results
EXAMPLE 6

Tables 4 to 6 detail the experimental performance test results for the blend formulation of example 6 according to the identified performance criteria of each of the two standards EN ISO 11611: 2007; EN ISO 11612: 2008


Performance Test—EN ISO 11611: 2007

Standard: Clause 6.1—tensile strength; Clause 6.2—tear strength; Clause 6.5—dimensional change; Clause 6.7—flame spread procedure A (surface ignition) and B (edge ignition); Clause 6.10—electrical resistance.


Pre-treatment: for 6.1, 6.2, 6.5 and 6.10 tests were made after 5 washing cycles in accordance with ISO 6330: 2000. Procedure 6A at 40° C. drying procedure E: tumble dry. The tumble drying was carried out after the completion of each wash. For 6.7 tests were made in the as received condition.









TABLE 3







Standard EN ISO 11611:2007 - Test results for the blend of example 6.













ISO 11611 Requirement &

PASS/Fail


Clause
Test Method
Performance Levels
Results
or Class















6.1***
ISO
Class 1 & 2
Warp
 970 N
LIKELY TO


Tensile strength
13934-1:1999
Min. of 400 N in both the warp
Weft
 890 N
MEET




and weft directions


CLASS 1 &







CLASS 2


6.2***
ISO
Class 1 & 2
Torn across warp
37.2 N
LIKELY TO


Tear strength
13937-2:2000
Min. of 20 N in both the warp and
Torn across weft
30.5 N
MEET



(electronic recording)
weft directions


CLASS 1 &







CLASS 2


6.5
ISO 5077
Class 1 & 2
Warp
Weft
FAIL


Dimensional

Max ± 3%
−4.5%
−5.0%











change

(−indicates shrinkage)
(−indicates shrinkage)



6.7****
ISO 15025:2000
Class 1 & 2
Procedures A & B
LIKELY TO


Limited

No flaming to top or side edge
No flaming to top or side edge
MEET


flame spread

No hole formation (A only)
No hole formation
CLASS 1 &


(procedures A & B)

No flaming or molten debris
No flaming or molten debris
CLASS 2




Mean afterflame ≦2 s
No afterflame




Mean afterglow ≦2 s
No afterglow


6.10
EN 1149-2:1997
Class 1 & 2
Resistance = 8.0 × 106
CLASS 1 &


Electrical Resistance*****

Electrical resistance greater than

CLASS 2




105 Ohms





***test made on two warpway and weftway specimens only


****test made on one warpway and weftway specimen only and without pre-treatment


*****sub contracted test made by STFI






Performance Test—EN ISO 11612: 2008

Standard: Clause 7.4—molten aluminium splash (D); Clause 7.5—molten iron splash (E); Clause 7.6—contact heat (F).


Pre-treatment: tests were made after 5 washing cycles in accordance with ISO 6330: 2000. Procedure 6A at 40° C. drying procedure E: tumble try. The tumble drying was carried out after the completion of each wash.









TABLE 4







Standard ISO 11612: 2008 - Test results for the blend of example 6.











ISO 11612 Requirement &





Performance Levels

PASS/Fail













Clause
Test Method
Performance levels
Min
Max
Results
or Class
















Molten AL splash (g)
Spec
Poured(g)
Skin stimulant
















7.4
ISO 9185
D1
100
<200
1
205
Damaged
LEVEL D1


Molten

D2
200
<350
2
102
Undamaged


Aluminium

D3
350

3
101
Undamaged


splash (D)




4
104
Undamaged







5
101
Undamaged













Molten Iron splash (g)
Spec
Poured(g)
Skin stimulant
















7.5
ISO 9185
E1
60
<120
1
201
Undamaged
LEVEL E3


Molten Iron

E2
120
<200
2
202
Undamaged


Splash (E)

E3
200

3
202
Undamaged







4
201
Undamaged













Threshold time(s)


















7.6
ISO 12127:
F1
5.0
<10.0
Specimen 1
4.6
NO LEVEL


Contact
1996 at 250° C.
F2
10.0
<15.0
Specimen 2
4.8


Heat (F)**

F3
15.0


Specimen 3


4.9








Result based
4.6







on lowest





**sub contracted test made by UKAS accredited laboratory






EXAMPLE 7

A fibre blend was ring spun on the cotton system to 60/2 Nm. The fabric was woven to a twill structure at approximately 190 gsm (or 5.5 oz per sq yd). The fibre blend comprised of 50% Protex™ C; 30% Helon FR viscose, 15% cotton and 15% para-aramid, with addition to 2% of antistatic fibres, all in intimate blend. Additional a reinforcement structure in the form of a grid at intervals of 10 ends and 10 picks was interwoven into the structure of the main fabric.


Performance Test Results for Example 7:—

Independent testing body: Vartest Laboratories, New York, USA Accredited to ISO/IEC 17025: 2005

    • Fabric submitted
    • PER NFPA 2112-2007 Specification
    • Fabric Code #: WAX 116-Protal-5
    • Finishing Details: Scour & Stenter only
    • Weight: 195 gsm, Ref Code #: WAX116
    • 49% Protex, 29% FR Viscose, 15% Cotton, 5% Aramid, 2% Anti-Static Color Royal Blue













Test Procedures:
Test Results:

















Fabric Weight (ASTM D3776):




As received:
5.44
oz/sq yd



184.55
grams/sq meter


After 100% laundering:
5.60
oz/sq yd



189.98
grams/sq meter


Thermal Protective Performance




Testing (NFPA 2112): Sections 7.1.1; 8.2




With Spacer:










As received:
Heat Transfer Rate:










10.5
cal/cm2/sec








After 3X MW per table 8.1.3:
Heat Transfer Rate:










11.2
cal/cm2/sec


Without Spacer:










As received:
Heat Transfer Rate:










7.6
cal/cm2/sec








After 3X MW per table 8.1.3:
Heat Transfer Rate:










7.9
cal/cm2/sec









Heat and Thermal Shinkage Resistance
NFPA 2112 Sections 7.1.2; 8.3





    • As received:


      Test temperature: 500° F., Test Exposure Time: 5 Minutes





Interpretation:

Minimum of Three items to be tested. Tested as received.


Immediately after specified exposure, the specimens shall be removed and examined for evidence of ignition, melting and dripping or separation.


Specimens shall be measured for shrinkage. Not to exceed 10% in either direction.


Dimensional change: Avg. Length Direction=−3.0%, Avg. Width Direction=−3.9%


Result: PASS when evaluated after heat at 500° F.


Heat and Thermal Shrinkage Resistance
NFPA 2112 Sections 7.1.4; 8.4





    • 3× per NFPA 2112 Section 8.1.3:





Test temperature: 500° F., Test Exposure Time: 5 Minutes


Interpretation:

Minimum of Three items to be tested. 3× per NFPA 2112 Section 8.1.3


Immediately after specified exposure, the specimens shall be removed and examined for evidence of ignition, melting and dripping or separation.


Specimens shall be measured for shrinkage. Not to exceed 10% in either direction.


Dimensional change: Avg. Length Direction=−5.4%, Avg. Width Direction=−5.8%


Result: PASS when evaluated after heat at 500° F.


NFPA 2112 Sections 7.1.2; 8.3
ASTM D6413
Flame Resistance of Textiles (Vertical)





    • as received





Length Direction
















After-flame (seconds)
After-glow (seconds)
Char length








0.0
1.9
22.0



0.0
3.0
40.0



0.0
4.0
26.0



0.0
3.0
25.0



0.0
1.6
32.0


Average
0.0
2.7
29.0









Width Direction
















After-flame (seconds)
After-glow (seconds)
Char length








0.0
3.5
25.0



0.0
4.3
25.0



0.0
3.6
32.0



0.0
3.4
24.0



0.0
4.3
25.0


Average
0.0
3.8
26.2





Comment: No melting or dripping occurred.






ASTM D6413
Flame Resistance of Textiles (Vertical)





    • after 100× laundering per NFPA 2112 Section 8.1.3:





Length Direction
















After-flame (seconds)
After-glow (seconds)
Char length








0.0
2.3
29.0



0.0
2.8
28.0



0.0
1.6
26.0



0.0
1.0
23.0



0.0
0.0
59.0


Average
0.0
1.6
33.0









Width Direction
















After-flame (seconds)
After-glow (seconds)
Char length








0.0
2.6
22.0



0.0
1.2
49.0



0.0
1.2
19.0



0.0
1.6
30.0



0.0
2.0
27.0


Average
0.0
1.7
29.4





Comment: No melting or dripping occurred.







NFPA 2112 Sections 7.1.5; 8.5 Predicted body Burn by Instrumented Manikin


Test according to the ISO13506 “Protective clothing against heat and flame, test method for complete garments, Prediction of burn injury using an instrumented manikin” European Test equivalent to ASTM F 1930


Independent testing body: Empa, Swiss Federal Laboratories for Materials Science and Technology St. Gallen, Switzerland









TABLE 5





Specimen identification (decl.)


Protal 5 with Grid


















Overall No1, size M
without
(Protal ® solutions
(blue)



pre-treatment
by Waxman)



50% Protex





30% FRV





15% cotton





 5% para-aramid


195 g/m2


Overall No2,
without
(wenaas antiflame)
(red)


size US 44
pre-treatment




50% Protex





30% FRV





15% cotton





 5% para-aramid


195 g/m2


Overall No3,
without
(wenaas antiflame)
(red)


size US 44
pre-treatment




50% Protex





30% FRV





15% cotton





 5% para-aramid


195 g/m2


without pre-treatment





Underwear





T-shirt white, Large


100% cotton


chest, 107-112 cm





Slip white, Medium


100% cotton


waist, 84-89 cm









2. Test Method

International Standard ISO 13506: 2008


“Protective clothing against heat and flame—Test method for complete garments—Prediction of burn injury using an instrumented manikin”


Principle

The test specimen was placed onto an adult sized manikin and exposed to a laboratory flash fire simulation with controlled heat flux, duration and flame distribution. Heat which was transferred through the test specimen during and after exposure was measured with the heat flux sensors. A software programme calculates the various degrees of burns and the total burn area.


Apparatus



  • Manikin Stationary, upright, adult-sized manikin fitted with 114 (122 incl. head) heat flux sensors excluding hands and feet.

  • Burner system consists of 12 burners (in pairs) located around the manikin, so that a uniform flame engulfment is achieved.



The complete procedure (manikin, burners and test room) is regulated with a special computer programme which also records the sensors' activities and calculates the various areas of burn and degrees of burn.


Test Conditions













Pre-treatment
without pre-treatment







Conditioning
≧24 h at (20 ± 2) ° C. and (65 ± 5) % r.h.


Heat flux
81.5 kW/m2 (Standard deviation 13.6);



duration of flame exposure 4 s


Sensors
before testing they must be clean,



dry and under 32° C.


Duration of flame exposure
3 s


Duration of data acquisition
60 s


Burn prediction model
combination of Stoll's and Takata's criteria


Gas
Propane


Samples
see Specimen identification









Description of Shrinkage Assessment Procedure

The measurements are taken on the fully dressed manikin. Length of fabric at specific points on the garment is measured with a metal ruler. Shrinkage is assessed as percentage of the measure after flame exposure to the one measured before.


3. Results

Table of burn prediction and graphical display of distribution of burns on the manikin. Total area of predicted pain, 1st, 2nd and 3rd degree burn injury (based on the area of manikin containing valid heat flux sensors) 60 s after beginning of flame exposure. Detailed information about the results of each sensor can be found in the attached tables.









TABLE 6





Average of samples 1-3







Ease measurements/shrinkage










mean value of three measurements











Avg. shrinkage
Standard deviation shrinkage


Location
[%]
[%]





Jacket length
−0.3
0.54


Arm length
1.2
0.41


Trousers length
6.8
2.46










Burn risk evaluation









mean values of three tests












2nd
3rd
2nd and 3rd
Transferred



Degree burn
Degree burn
Degree burn
energy



[%]
[%]
[%]
[kJ]















Body part
Mean
SD1
Mean
SD1
Mean
SD1
Mean
SD1





Chest
40.0
17.3
0.0
0.0
40.0
17.3
28.7
1.1


Stomach
2.8
4.8
0.0
0.0
2.8
4.8
20.7
1.6


Upper back
30.5
4.8
5.5
4.8
36.1
4.8
41.4
1.1


Lower back
0.0
0.0
0.0
0.0
0.0
0.0
28.4
0.3


Left arm
40.0
10.0
3.3
5.8
43.3
5.8
33.1
0.6


Right arm
43.3
15.3
10.0
10.0
53.3
11.5
34.8
0.6


Left leg
26.4
2.4
0.0
0.0
26.4
2.4
68.1
1.2


Right leg
11.6
16.5
2.9
2.5
14.4
14.0
62.5
3.9


Complete
22.2
1.3
2.3
1.3
24.6
2.3
317.7
6.0


manikin
















TABLE 7





Results of informative test no. 1







Shrinkage assessment













Specimen
Specimen





before
after




Manikin data
testing
testing
Shrinkage


Location
[cm]
[cm]
[cm]
[%]





Jacket length
Colar to hem
53.0
53.5
−0.9


Arm length
Shoulder to sleeve
61.3
60.3
1.6


Trousers length
Inside leg
82.0
75.0
8.5










Burn prediction













Pain
1st degree
2nd degree
3rd degree
Transferred


Body part
[%]
burn [%]
burn [%]
burn [%]
energy [kJ]





Chest
10.0
20.0
20.0
0.0
27.4


Abdomen
0.0
0.0
8.3
0.0
22.4


Upper back
66.7
0.0
25.0
8.3
40.9


Lower back
30.8
0.0
0.0
0.0
28.7


Left arm
50.0
0.0
30.0
10.0
33.6


Right arm
30.0
0.0
40.0
20.0
35.4


Left leg
54.2
0.0
29.2
0.0
69.4


Right leg
56.5
0.0
30.4
0.0
66.8


Total
41.2
1.8
23.7
3.5
324.6









Observations





    • after flame time approx. 6 s

    • high smoke production

    • change of colour












TABLE 8





Results of informative test no. 2







Shrinkage assessment













Specimen
Specimen





before
after




Manikin data
testing
testing
Shrinkage


Location
[cm]
[cm]
[cm]
[%]





Jacket length
Colar to hem
57.0
57.0
0.0


Arm length
Shoulder to sleeve
61.3
60.5
1.2


Trousers length
Inside leg
77.0
71.0
7.8










Burn prediction













Pain
1st degree
2nd degree
3rd degree
Transferred


Body part
[%]
burn [%]
burn [%]
burn [%]
energy [kJ]





Chest
10.0
0.0
50.0
0.0
29.4


Abdomen
0.0
0.0
0.0
0.0
19.1


Upper back
50.0
0.0
33.3
8.3
42.6


Lower back
15.4
0.0
0.0
0.0
28.1


Left arm
30.0
10.0
50.0
0.0
33.2


Right arm
50.0
0.0
30.0
10.0
34.4


Left leg
45.8
8.3
25.0
0.0
67.8


Right leg
56.5
4.3
4.3
4.3
59.6


Total
36.0
3.5
21.1
2.6
314.3









Observations





    • after flame time approx. 4 s

    • high smoke production

    • change of colour












TABLE 9





Results of informative test no. 3







Shrinkage assessment













Specimen
Specimen





before
after




Manikin data
testing
testing
Shrinkage


Location
[cm]
[cm]
[cm]
[%]





Jacket length
Colar to hem
57.0
57.0
0.0


Arm length
Shoulder to sleeve
61.0
60.5
0.8


Trousers length
Inside leg
76.0
73.0
3.9










Burn prediction













Pain
1st degree
2nd degree
3rd degree
Transferred


Body part
[%]
burn [%]
burn [%]
burn [%]
energy [kJ]





Chest
10.0
0.0
50.0
0.0
29.3


Abdomen
0.0
0.0
0.0
0.0
20.8


Upper back
50.0
0.0
33.3
0.0
40.7


Lower back
23.1
0.0
0.0
0.0
28.2


Left arm
20.0
20.0
40.0
0.0
32.5


Right arm
40.0
0.0
60.0
0.0
34.5


Left leg
50.0
0.0
25.0
0.0
67.1


Right leg
69.6
4.3
0.0
4.3
61.0


Total
38.6
2.6
21.9
0.9
314.1









Observations





    • after flame time approx. 4 s

    • high smoke production

    • change of colour





Test Type—EN ISO 14116: 2008



  • Independent testing body: West Yorkshire Material Testing Service, Leeds, UK
    • Fabric submitted
    • Fabric Code: Protal-5 with Para-aramid Grid
    • Finishing details: Scoured and Stenter only
    • Weight: 195 gsm, Ref Code: WAX118
    • 50% Protex, 30% So FRV, 15% Cotton, 5% Para-aramid with 2% overall anti-static added

  • Performance Standard: Testing to EN ISO 14116: 2008
    • Clause 6.1 Thermal performance—
    • Limited flame spread Procedure A (surface ignition)
    • Clause 6.2.1 Tensile strength
    • Clause 63.2.2 Tear Strength

  • Pre-treatment: Tests were made after 5 washing cycles in accordance with ISO 6330: 2000
    • Procedure 2A at 60° C. Drying Procedure E. The tumble drying was carried out after the completion of each wash.










TABLE 10







Test results for example 7.













EN ISO 14116 Requirements




Clause
Test Method
& Performance Levels
Results
Comments





6.1 Limited flame
ISO 15025:2000
Index 1
As received
Index


spread Procedure

No flaming to top or side edge
No flaming to top or side
3/5H/60


A (surface

No flaming debris
edge



ignition

No afterglow shall spread
No flaming debris





from the carbonized area to
No afterglow





the undamaged area
No hole formation





Index 2
No afterflame





No flaming to top or side edge
After 5 washing cycles





No flaming debris
No flaming to top or side





No afterglow shall spread
edge





from the carbonized area to
No flaming debris





the undamaged area
No afterglow





Index 3
No hole formation





No flaming to top or side edge
No afterflame





No flaming debris






No afterglow shall spread






from the carbonized area to






the undamaged area






No hole formation






Afterflame time of each






individual specimen shall not






exceed 2 s




6.2.1
ISO 13934-
Min. of 150N in both the warp
As received
PASS











Tensile strength
1:1999
and weft directions
Warp
580N





Weft
400N









After 5 washing cycles










Warp
520N



Weft
400N











6.2.2
ISO 13937-
Min of 7.5N
As received
PASS











Tear Strength
2:2000

Torn across warp
39N



(electronic

Torn across weft
33N











recording)

After 5 washing cycles










Torn across warp
37N



Torn across weft
32N









Test Type—BS EN 1149-3 Method 2



  • Independent testing body: West Yorkshire Materials Testing Service, Leeds, UK
    • Fabric submitted
    • Fabric code: Protal-5—with Para-aramid Grid
    • Finishing details: Scoured and Stenter only
    • Weight: 195 gsm, Ref Code: WAX118
    • 50% Protex, 30% So FRV, 15% Cotton, 5% Para-aramid with 2% overall anti-static added

  • Test Required: Induction Decay

  • Pre-treatment: Tests were made after 5 washing cycles in accordance with ISO 6330: 2000
    • Procedure 2A at 60° C. Drying Procedure E. The tumble drying was carried out after the completion of each wash



Determination of Width Between Conductive Threads

The width of gap between the conductive threads was measured in five areas with a steel rule.














Width of Gap (mm)



















5.0




5.0




5.0




5.0




5.0



Mean
5.0









Determination of Induction Decay Time

The sample was conditioned and tested at 23+/−1° C. and 25+/−5% r.h.


The charge decay time and shielding effect were measured according to BS EN 1149-3: 2004 Method 2 (induction charging)















Shielding Factor (S)
Half Decay Time, t50 (Secs.)




















0.93
<0.01




0.93
<0.01




0.92
<0.01



Mean:
0.93
<0.01









Comments:

Based on the tests carried out on the sample supplied:


a) for a material containing conductive threads in a stripe or grid pattern the spacing of the conductive threads in one direction shall not exceed 10 mm.


b) the results of BS EN 1149-3 Method 2: 2004 meet the requirements specified in BS EN 1149-5: 2008 of the shielding factor being greater than 0.2 and/or the half decay time being less than 4 seconds.


Test Type—EN ISO 11612: 2008



  • Independent testing body: West Yorkshire Materials Testing Service, Leeds, UK
    • Fabric submitted
    • Fabric code: Protal-5—with Para-aramid Grid
    • Finishing details: Scoured and Stenter only
    • Weight: 195 gsm, Ref Code: WAX118
    • 50% Protex, 30% So FRV, 15% Cotton, 5% Para-aramid with 2% overall anti-static added

  • Performance Standard: Testing to EN ISO 11612: 2008
    • Clause 6.2 Heat resistance
    • Clause 6.3 Limited flame spread (A1 surface ignition and A2 edge ignition)
    • Clause 6.4 Dimensional change
    • Clause 6.5.1 Tensile strength
    • Clause 6.5.2 Tear strength
    • Clause 7.2 Convective heat (B)
    • Clause 7.3 Radiant heat (C)

  • Pre-treatment: Tests were made after 5 washing cycles in accordance with ISO 6330: 2000
    • Procedure 2A at 60° C. Drying Procedure E. The tumble drying was carried out after the completion of each wash.
    • For clause 6.3 tests were made both before and after the 5 washing cycles as described above.



In accordance with Annex G of EN ISO 11612: 2008 the uncertainty of measurement associated with the test methods was not taken into account.









TABLE 11







Test results for example 7.













EN ISO 11612 Requirements

Pass/fail or


Clause
Test Method
& Performance Levels
Results
Level





6.1 Heat
ISO 17493:2000
180° C.
180° C.
PASS


resistance
at 180° C. and
No ignition
No ignition




260° C.
No melting
No melting





Maximum shrinkage 5%
Shrinkage












260° C.
Warp
−3.5%



No ignition
Weft
−2.7%











No melting
260° C.
PASS



Maximum shrinkage 10%
No ignition




(−indicates shrinkage)
No melting





Shrinkage











Warp
−4.5%



Weft
−5.2%











6.3 Limited flame
ISO 15025:2000
No flaming to top or side edge
Surface Ignition as
PASS


spread

No hole formation (A1 only)
received and after 5
A1


(A1 and A2)

No flaming, melting or molten
washing cycles





Debris
No flaming to top





Mean after flame ≦2 s
or side edge





Mean afterglow ≦2 s
No hole Formation






No flaming,






melting or molten






debris






No afterflame






No afterglow






Edge
PASS





Ignition as received
A2





and after 5 washing cycles






No flaming to top






or side edge






No flaming,






melting or molten






debris






No after flame






No afterglow













6.4
ISO 5077
Maximum ± 3%
Warp
−3.5%
FAIL


Dimension

(−indicates shrinkage)
Weft
Nil



change







6.5.1
ISO 13934-
Minimum 300N in both warp
Warp
520N
PASS


Tensile strength
1:1999
and weft direction
Weft
400N













6.5.2
ISO 13937-
Minimum 15N in both warp
Torn across warp
37N
PASS


Tear Strength
2:2000
and weft direction
Torn across weft
32N




(electronic







recording)
















7.2
ISO 9151:1995
Range of HTI24 Values (s)
Specimen 1
6.4
LEVEL


Convective heat

Performance Levels
Specimen 2
6.5
B1













(B)


Min.
Max
Specimen 3
6.5




B1
 4.0
<10.0
Result based
6.4




B2
10.0
<20.0
on lowest





B3
20.0

HTI24













7.3
ISO 6942:2002
Heat Transfer Factor of
Specimen 1
13.4
LEVEL


Radiant heat(C)
Method B heat
RHTI24 Performance Levels
Specimen 2
13.1
C1














flux 20 kW/m2

Min.
Max
Specimen 3
13.1




C1
 7.0
<20.0
Result based
13.1




C2
20.0
<50.0
on lowest





C3
50.0
<95.0
RHTI24





C4
95.0









Test Type—Analysis for the Extractable Antimony Content
Test Method OTS 100

Independent testing body: Shirley Technologies Ltd, Manchester, UK


Article Description: Blue dyed woven fabric Ref: Protal 5 NG/WAX-129


Introduction

Blue dyes woven fabric sample was submitted for testing the extractable antimony content.


Sample Details

The samples submitted were as follows:


Sample 1: Blue dyed woven fabric

    • Ref: Protal 5 NG
    • 50% Protex, 30% FR Viscose, 15% Cotton, 5% Para-aramid
    • Waxman code: WA-129


Laboratory Investigation

The sample was extracted in artificial sweat solution and analysed on the inductively coupled plasma (ICP)


Results















Sample
Antimony (mg/kg)








Blue dyed woven fabric Ref:
23.20



Protal 65 NG/WAX-129









Detection limit of this test is—0.8 mg/kg









TABLE 12







Limit values and Fastness for TEST METHOD OTS 100













II
III
IV



I
in direct contact with
with no direct contact with
Decoration


Product Class
Baby
skin
skin
material










Limit values and fastness, part 1





pH value1












4.0-7.5
4.0-7.5
4.0-9.0
4.0-9.0







Formaldehyde [mg/kg]











Law 112
n.d.2
75
300
300







Extractable heavy-metals [mg/kg]











Sb (Antimony)
30.0
30.0
30.0



As(Arsenic)
0.2
1.0
1.0
1.0


Pb (Lead)
0.2
1.03
1.03
1.03


Cd (Cadmium)
0.1
0.1
0.1
0.1


Cr (Chromium)
1.0
2.0
2.0
2.04








Cr (VI)
under detection limit5











Co (Cobalt)
1.0
4.0
4.0
4.0


Cu (Copper)
25.06
50.06
50.06
50.06


Ni (Nickel)7
0.5
1.0
1.0
1.0


Mg (Mercury)
0.02
0.02
0.02
0.02







Heavy metals in digested sample [mg/kg]8











Pb (Lead)
90.0
90.03
90.03
90.03


Cd (Cadmium)
50.0
100.03
100.03
100.03







Pesticides [mg/kg]9, 10











Sum10
0.5
1.0
1.0
1.0







Chlorinated phenols [mg/kg]10











Pentachlorophenol (PCP)
0.05
0.5
0.5
0.5


Tetrachlorophenol (TeCP)
0.05
0.5
0.5
0.5


Sum










Limit values and fastness, part 2





Pathalates [w. %]11











DINP, DNCP, DEHP, DIOP, BBP, DBP,
0.1





DIBP, DIHP, DHNUP, DHP, DMEP, DPP,






Sum10






DEHP, BBP, DBP, DIBP, DIHP, DHNUP,

0.1
0.1
0.1


DHP, DMEP, DPP, Sum10











Organic tin compounds [mg/kg]10











TBT
0.6
1.0
1.0
1.0









General Performance Results

The performance test results, for examples 3 and 6 confirm the fabrics satisfy all of the desired requirements. In particular, the blend of example 3 was found to perform better than the blend of example 6 with regard to tensile strength, tear strength, electrical and contact heat resistivity. The Oekotex standard requirements were also satisfied for both samples 3 and 6 following respective testing.


The performance test results for Example 7 show compliance with both the sections of US Standard NFPA 2112 which relate to a fabric (namely Sections 7.1.1, 7.1.2, 7.1.3, 7.1.4 and 7.1.5) as well as the EU standards EN11612, and EN14116 for FR performance of garments, with EN1149-5 for anti-static performance and thus shows a “Universal Compliance”: the test results for Oekotex100 limit for extractable antimony illustrates that the fabric would conform to the whole Oekotex 100 requirement as there is known compliance for all other elements.


The presented results confirm that the present fibre blend based on the combination of a modacrylic with a natural cellulosic material and a FR viscose, at the appropriate weight % is capable of satisfying different performance standards with regard to fabric safety. This is perhaps contrary to expectation as, for example, cotton fibres are not considered to be inherently flame resistant and are susceptible to burn. The inventors have realised a synergistic affect between the blend of a modacrylic with a natural cellulosic (natural cotton) and FR viscose. The effect is manifested in an observed increase in the combined limited oxygen index (LOI) of the fabric wherein the LOI of the blend is greater than the sum of the LOI of the individual components. As will be appreciated, the LOT refers to the minimum concentration of oxygen that will just support flaming combustion of a material. The affect of incorporating a natural cellulosic may be considered to increase the charring affect of fabric when exposed to extreme heat which increases the LOI by expelling oxygen within the matrix as the charred carbon barrier forms during initial heat contact.


The present invention is therefore advantageous for use as a ‘universal’ protective fabric that has exhibited proven performance as a protective layer to flame, electric discharge and molten metal hazards.


Fabric Construction

A fibre blend comprising 50% Protex™; 30% Helon FR viscose; 15% cotton 5% para-aramid was mixed, carded, drawn, roved, spun and wound to create a yarn according to a first yarn type. A second yarn type having a two-ply construction was formed by the same spun yarn process of as the first yarn using a fibre blend comprising a 50% by weight para-aramid (for example KEVLAR by E.I. Du Pont de Nemours and Co) and 50% by weight of the fibre blend of the first fibre type.


A woven fabric was constructed using the first yarn type as a majority component via interweave of warps and wefts. The second yarn type was interwoven with the first yarn type (as a single weave assembly) at every 10 ends and 10 picks (with respect to warps and wefts). Accordingly, the resulting fabric structure comprised predominantly warps and wefts of the first yarn type and interwoven warps and wefts of the second yarn type spaced at regular intervals to create a grid network repeated every 10 ends and 10 picks.

Claims
  • 1. A flame retardant yarn having a composite structure formed from a collection of fibres twisted together, the fibres comprising a blend of: 40% to 60% by weight of a modacrylic;5% to 25% by weight of a naturally occurring cellulosic material; and20% to 40% by weight of a FR viscose based material.
  • 2. The yarn as claimed in claim 1 wherein the modacrylic comprises a copolymer of: acrylonitrile; andvinyl chloride and/or vinylidene chloride.
  • 3. The yarn as claimed in claim 1 wherein the modacrylic comprises: 30% to 70% by weight of acrylonitrile; and70% to 30% by weight of vinyl chloride and/or vinylidene chloride.
  • 4. The yarn as claimed in claim 1 wherein the modacrylic comprises vinylidene chloride and antimony oxide.
  • 5. The yarn as claimed in claim 4 wherein the antimony oxide comprises antimony trioxide.
  • 6. The yarn as claimed in claim 4 wherein the antimony oxide comprises antimony pentoxide.
  • 7. The yarn as claimed in claim 1 wherein the naturally occurring cellulosic material comprises any one or a combination of: Cotton;Bamboo;Linen; and/orJute.
  • 8. The yarn as claimed in claim 1 further comprising nylon.
  • 9. The yarn as claimed in claim 8 comprising trace to 7% by weight nylon.
  • 10. The yarn as claimed in claim 8 comprising trace to 5% by weight nylon or a para-aramid.
  • 11. The yarn as claimed in claim 1 further comprising trace to 5% by weight of an antistatic material.
  • 12. The yarn as claimed in claim 1 comprising: 40% to 55% by weight of the modacrylic;10% to 20% by weight of the naturally occurring cellulosic material; and25% to 35% by weight of the FR viscose based material.
  • 13. The yarn as claimed in claim 1 comprising: 45% to 55% by weight of a modacrylic comprising a copolymer of acrylonitrile and a halogen-containing vinyl monomer, the copolymer further comprising antimony pentoxide;10% to 20% by weight of natural cotton;25% to 35% by weight of FR viscose;trace to 7% by weight nylon; andtrace to 5% by weight of a carbon based antistatic material.
  • 14. A fabric comprising fibres according to claim 1.
  • 15. The fabric as claimed in claim 14 wherein the fabric is woven, knitted or non-woven.
  • 16. A garment comprising the fabric according to claim 14.
  • 17. A flame retardant fibre blend comprising: 40% to 60% by weight of a modacrylic;5% to 25% by weight of a naturally occurring cellulosic material;20% to 40% by weight of a FR viscose based material; and5 to 20% by weight of a thermostable fibre that exhibits no appreciable decrease in mechanical strength after exposure to heat or flame in excess of 500° C.
  • 18. The fibre blend as claimed in claim 17 wherein the thermostable fibre comprises any one or a combination of: meta-aramid;para-aramid;polybenzimidazole;p-phenylene benzobisoxazole (PBO);polysulphonamide (PSA);a polyamide-imide (PAI);melamine;carbon fibre; and/orglass fibre.
  • 19. The fibre blend as claimed in claim 17 wherein the thermostable fibre is a blend including any one or a combination of: 5 to 95% by weight of the thermostable fibre being any one or a combination of:
  • 20. The fibre blend as claimed in claim 17 further comprising an antistatic fibre included in the range of trace to 10% by weight.
  • 21. A yarn or filament formed from the fibre blend according to claim 17.
  • 22. A fabric formed from at least one yarn or filament as claimed in claim 21.
  • 23. The fabric as claimed in claim 22 comprising a woven, non-woven, knitted or braided construction.
  • 24. A flame retardant fabric having a composite structure comprising: a first yarn forming a majority component of the fabric, the first yarn having a composition comprising: 40% to 60% by weight of a modacrylic;5% to 25% by weight of a naturally occurring cellulosic material; and20% to 40% by weight of a FR viscose based material; anda second yarn and/or filament type forming a minority component of the fabric, the second yarn and/or filament type comprising a thermostable stable fibre that exhibits no appreciable decrease in mechanical strength after exposure to heat or flame in excess of 500° C.
  • 25. The fabric as claimed in claim 24 wherein the thermostable fibre comprises anyone or a combination of: meta-aramid;para-aramid;polybenzimidazole;p-phenylene benzobisoxazole (PBO);polysulphonamide (PSA);a polyamide-imide (PAI);melamine;carbon fibre; and/orglass fibre.
  • 26. The fabric as claimed in claim 24 wherein the thermostable fibre is a blend including any one or a combination of: 5 to 95% by weight of the thermostable fibre being any one or a combination of: meta-aramid, para-aramid, polybenzimidazole, p-phenylene benzobisoxazole (PBO), polysulphonamide (PSA), a polyamide-imide (PAI), melamine, carbon fibre, and/or glass fibre;30 to 70% by weight of the modacrylic;30 to 70% by weight of the FR viscose based material; and5 to 20% by weight of the naturally occurring cellulose material.
  • 27. The fabric as claimed in claim 24 further comprising an antistatic fibre included in the range of trace to 10% by weight.
  • 28. The fabric as claimed in claim 24 further comprising a woven structure: wherein a majority of the warps and wefts of the weave comprise the first yarn type; andwherein the second yarn and/or filament type is interwoven as warps and wefts at spaced apart intervals amongst the warps and wefts formed from the first yarn type.
  • 29. A woven fabric as claimed in claim 28 wherein the second yarn and/or filament type is interwoven with the first yarn type at a regular spacing in the range of 5 to 15 ends and in the range of 5 to 15 picks.
  • 30. A woven fabric as claimed in claim 28 wherein the second yarn and/or filament type is interwoven with the first yarn at a regular spacing in 10 ends and 10 picks.
  • 31. A garment comprising the fabric according to claim 15.
Priority Claims (2)
Number Date Country Kind
GB0813401.7 Jul 2008 GB national
PCT/GB2009/050676 Jun 2009 GB national
Parent Case Info

This application is a continuation-in-part of U.S. patent application Ser. No. 13/055,239, filed on Apr. 4, 2011, which claims priority to and all the benefits of International Patent Application Ser. No. PCT/GB2009/050676, filed on Jun. 15, 2009, which claims priority to and all the benefits of Great Britain Patent Application Ser. No. GB0813401.7, filed on Jul. 22, 2008, each of the specifications of which is incorporated herein by reference in its entirety.

Continuation in Parts (1)
Number Date Country
Parent 13055239 Apr 2011 US
Child 13842988 US