专利摘要:
Sheet-like textile structures consist of fibres possessing a modulus of elasticity of 200 to 2500 daN/mm<2> and, before curing, have an extensibility in the longitudinal direction of more than 10%. The sheet-like textile structures coated or impregnated with reactive resin can be used as structural materials, in particular as fixed dressings in medicine or for industrial apparatuses.
公开号:SU1600623A3
申请号:SU884355960
申请日:1988-06-23
公开日:1990-10-15
发明作者:Рихтер Роланд;Майер Вольфрам;Ланген Гюнтер;Лейзер Вилли
申请人:Байер Аг (Фирма);Карл Отто Браун Кг (Фирма);
IPC主号:
专利说明:

The invention relates to a technique for producing webs that can be used in the production of molded articles used in medicine and technology, in particular, to methods for producing textile webs.
The purpose of the invention is to increase the stretchability of a textile web.
The goal is achieved by preliminarily making a textile carrier from organic fibers and treating it with a water-curable plastic resin, using organic fibers with an elastic modulus of 200 to 2500 daN / mm in quantity, providing a weight of 40 to 300 g / m, moreover, prior to treatment with a water-curable plastic resin, the carrier
subjected to thermal shrinkage and / or wet shrinkage.
The treatment can be carried out by impregnation and / or coating.
Thermal shrinkage is carried out either with air at a temperature of 80-250 ° C, or with water or superheated steam at a temperature of 100-80 seconds for 0.1- 60 minutes. Wet shrinkage is carried out by immersing and / or impregnating the carrier with a liquid medium, such as water, alcohol, if necessary in the presence of auxiliary agents, such as surfactants.
After treatment with a plastic resin, hardened with water, textile fabric is stored for lack of moisture.
ABOUT)
about:
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The proposed textile fabric is distinguished by stretchability in both the riverine and longitudinal directions of the river.
Longitudinal direction means the direction of textile processing, i.e. "; for example, by aligning the base or stitch columns
The transverse direction means the direction, the vertical direction of processing of the canvas, Toe. the direction of the weft yarns or loops.
The proposed textile web may have various geometric shapes, the preferred shape of the ribbon, or 1-1. How long is the side of the ribbon in accordance with the processing direction of the textile fabric The ribbon may be a fabric, knit, knitted fabric or canvas.
Natural or chemical fibers can be used as organic fibers, and as natural fibers — in particular, vegetable fibers of seeds and fruits such as cotton fibers, bast fibers (hemp and jute) and hard fibers (sisal). Preferably use in particular cotton fibers.
Synthetic polymers can be used as chemical fibers, for example, carbon chain fibers such as polyethylene, polypropylene, polychloride (for example, polyvinyl chloride and polyvinylidene chloride), polyacrylate and vinyl acetate fibers, hetero fibers, such as as polyamide, polyester and polyurea fibers, and polyaddition fibers obtained, such as spandex and elastano
It is also possible to use viscose or elastodiene (rubber fibers.,
Preferred synthetic fibers are polyester, polyamide, and polyacrylonitrile fibers.
It is also possible to produce textile fabric from various fibers, preferably from polyester and / or polyamide and / or cotton fibers.
textiles are preferred when using plant fibers
five
0
Mixed yarn cloths, and in the longitudinal direction they use V9s from synthetic polymer, and in the transverse direction from vegetable fibers
Preferably in the longitudinal direction, the yarn system provides, after the shrinking process, elastic stretching in the longitudinal direction. In the case of using natural fiber yarns, high twist yarns or twisted staple yarns with a twist factor of about 120 to 600 are preferred so that high twist is ensured high torque and, consequently, the tendency to form sucrutino The twist factor ". is determined by the equation
0 / T
five
0
five
0
five
0
five
where t
THOSE
torsion number per 1 meter of yarn or twisted yarn; - mass dependent
in g / 1 000 m in order to avoid unwanted torsion of a textile fabric - the threads are preferably produced by a variable direction of torsion (clockwise S torsion, counterclockwise Z torsion), namely in an alternate order, for example, one thread S - one Z thread or two S threads - two Z threads.
I
As threads with long
elasticity can be used as fibers from natural rubber (for example, from elastodiene), and fibers from polyurethane elastomeric fibers (for example, from elastane),
To achieve longitudinal extensibility, complex textured yarns made of polyester, polyamide fibers and Todo are used as chemical fibers.
The elastic properties of these complex yarns are based on the constant Twisting and torsion of the yarns achieved during the texturing process, which is ensured by the thermoplastic properties of the materials. It is possible to use all types of textured yarns, such as, for example, high stretch textured nnti, textured yarns with reduced stretch, high volume yarns.
The yarn connection in the longitudinal system is provided with wrap yarns, and it is possible to use both staple or twisted yarns from natural fibers and staple or multifilament yarns (satin yarns) from chemical fibers. The strength characteristics of these yarns are used elastic modulus.
Before curing with a plastic resin, the proposed textile fabric has a stretch in the longitudinal direction of 15-2007. By stretchability in the longitudinal direction is understood to be a change in length compared to a completely weakened textile cloth, which is achieved by loading the textile cloth in the longitudinal direction (10 N / 1 cm wide).
Polymers based on polyurethane or polyvinyl resins are preferably used as water-curable plastic resins.
The proposed web is preferably used for supporting dressings in medicine and veterinary medicine, they are distinguished by the comfort of application of the Toe. limbs of humans and animals without wrinkling can be found in difficult places, such as knees, elbows and felts.
Example 1, Preparation of water-curable plastic resins.
Textile carriers according to TabLo 1 are crushed with resins.
Prepolymer I.
100 hours of technical polyphenyl polymethylene polyisocyanate, obtained by phosgenating aniline condensate and formaldehyde (ijyoc 200 NCO content 31%), is reacted with 32.2 h of propoxylated triethanolamine (hydroxyl number 150 mg KOH / g). A prepolymer is obtained with an NCO content of 20.0% and with a viscosity of 1 20000 mPa-s. The content of the catalyst is 0.30% tert-amino nitrogen.
Prepolymer II
660.0 hours Bis- (4-isodianatophenyl) -methane containing carbodiimidated units (NCO content 29%) is reacted with HWHP of propoxylated triethanolamine
(g id rock stronger than 150 mg KOH / g). To the resulting formaldehyde add 1 h. polydimethylsiloxane with a viscosity of mPa-s, and 15 hours of an ultra-violet stabilizer (a derivative of cyanoalkylindol) “The resulting former polymer has a tfc viscosity of –23000 Mna iC and contains 13.5% isoprene and 0.45% tert. nitrogen, Prepolymer III,
In a container equipped with a stirrer, 6.48 g of isocyanate of bis- (4-isocyanatophenyl) methane, containing 5 carbodiimidated units, is fed. Then, 7.8 g of polydimethylsiloxane with a viscosity of 30,000 g / mol and 4.9 g of benzoyl chloride are added, after which another 1.93 kg of polyether obtained by propoxylation of propylene glycol (hydroxyl number 112 mg KOH / g), 1, is added 29 kg of polyester glycerin obtained by propoxylation (hydroxyl number: 5 mg of 250 mg KOH / g) and 190 g of dimorpholine diethyl ether. After 30 minutes the reaction temperature. is, and after.
60 minutes, the maximum temperature is reached. 500 g of polydimethylsiloxane with a viscosity of 2.5 C 100 mPa I s are added and stirred. The viscosity of the finished prepolymer is 15700 mPa-ic, the content of isocyan-J is 12.9%
Prepolymer IV.
100 parts of a technical polyfestock-polymethylene polyisocyanate obtained by phosgenation of aniline Q condensate and formaldehyde (j, 200 mPa1-s, NCO content 31%), is reacted with 32.2 parts of ethoxylated triethanolamine (hydroxyl number 149 mg KOH / g).
5 A prepolymer is obtained with an NCO content of 18.9% and a viscosity of Ta5 ° g of 28,000 mPa t s. The content of the catalyst is 0.3% tert-amine nitrogen.
The carrier is thermally shrunk in a drying cabinet, for example, steam water for 5 minutes with or heated air for 10 minutes at 35 s. If necessary, dried at 1I0- g 190 C in order to completely remove the residual moisture. Coatings of prepolymers I-IV are carried out in a dry chamber, the relative humidity of which is characterized by a dew point.
water below -ZO Co The resin is applied in such a way that first the weight of the required length of the textile knit fabric is determined and then the amount of the prepolymer needed to achieve sufficient adhesion is applied to the knitted tape. The prepolymer is then dissolved in methylene chloride, a tricottape is impregnated with the resulting solution and then the solvent is removed in vacuo. The retention of the resin depends on the purpose of the web. For menfni as synthetic
supporting substrates, the content of cMoibi is 35-65%, while when used in engineering, for example, as an insulation or feasible full of all loop holes (applied amount more than 65% of the total Becii) . The tapes of the required length with the applied coating, in the state of released internal stresses, are sealed in a package of non-admissible water vapor of the film,
The data on the prepolymers 1 used and the stretchability of the textile fabric are not given in Table. 2o
Formula of the invention
权利要求:
Claims (4)
[1]
1. A method for producing a textile web, wherein
A textile carrier is made from organic fibers and treated with a water-curable plastic resin, characterized in that organic fibers with an elastic modulus of 200 to 2500 daN / MM are used as organic fibers to provide a surface weight. AO blades - 300 g / m, and before treatment with water-curable plastic resin, the carrier is subjected to thermal and / or wet shrinkage
[2]
2. A method according to claim 1, in accordance with claim 1, so that thermal shrinkage is carried out with air
80 - 250 C or steam at 100 to within 0.1-60 min.
[3]
3. A method according to claim 1, characterized in that the wet shrinkage is carried out by immersing and / or impregnating the carrier with a liquid medium.
[4]
4. The method according to claim 3, characterized by the fact that the wet shrinkage is carried out in the presence of an auxiliary agent.
I
about p and t. e on punkp r and and m: 24-06.08.8 on pr
one
07.08-87 on Ave. 3
2 A
Textile Linen Indicators
Table 1
Note.
PES-TEXS: 167 dtex, f 30x2, complex textured
polyester thread (highly elastic yarn, K 62%)
PES-TEX: 167 dtex, f 30x1, complex textured
polyester thread (highly elastic yarn, K 60%)
PES-HFs 550 dtex, f 96 VZ 60, complex high strength
polyester thread, normal shrinkage, E 1650 daN / mm
PE & -GL: 167 dtex, f 32) 2, complex polyester thread
PES-NS; 830 dtex, f 200, complex high-strength polyester filament, but 1 is 1 shrinkage, Е И70 daN / mm
PES-MF.: 550 dtex, f 96, complex high-strength polyester thread, low shrink, Y 980 daN / mm
PES / STM A5 dtex "l, normal polyester yarn (staple fiber)
RA 1: software dtex, f, complex textured
polyamide yarn (highly elastic thread, K 61%)
PA 2:78 dtex, f 17x2, complex textured polyamide yarn (highly elastic yarn, K 66%).
K - equitability according to the industrial standard of the Federal Republic of Germany 53 840.
E is the modulus of elasticity.
34.4
42,8
55,6
56.0
53.0
57.2
34.9
42.4
53.2
23.7
65.9
82.2
table 2
80
68
80
74
70
48
84
60
45
74
90
64
37.5
35.0
13
24
25
25
53
18
sixteen
26
62
47
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同族专利:
公开号 | 公开日
IL86817D0|1988-11-30|
AU1836988A|1989-01-05|
DK345788A|1988-12-25|
IL86817A|1991-08-16|
IE61729B1|1994-11-30|
HU212119B|1996-02-28|
IE881917L|1988-12-24|
FI883007A0|1988-06-22|
FI883007A|1988-12-25|
CA1330917C|1994-07-26|
NO882524D0|1988-06-08|
NO176615B|1995-01-23|
CN1031081C|1996-02-21|
KR890000240A|1989-03-13|
FI95934B|1995-12-29|
EP0301214A3|1991-07-31|
PT87787B|1994-03-31|
DK174216B1|2002-09-30|
BR8803090A|1989-01-31|
PT87787A|1989-05-31|
AU608622B2|1991-04-11|
DE3726268A1|1989-01-05|
JPS6414377A|1989-01-18|
DK345788D0|1988-06-23|
PH26348A|1992-04-29|
NO882524L|1988-12-27|
US4940047A|1990-07-10|
NO176615C|1995-05-03|
EP0301214B1|1993-09-01|
DE3883660D1|1993-10-07|
EP0301214A2|1989-02-01|
CN1030269A|1989-01-11|
ES2042650T3|1993-12-16|
HUT50231A|1989-12-28|
FI95934C|1996-04-10|
KR960009086B1|1996-07-10|
AT93909T|1993-09-15|
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法律状态:
优先权:
申请号 | 申请日 | 专利标题
DE3720762|1987-06-24|
DE19873726268|DE3726268A1|1987-06-24|1987-08-07|TEXTILE AREA WITH REACTIVE RESIN|
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