EP0675215B1

EP0675215B1 - A process for preparing a thermal bondable fiber

Info

Publication number: EP0675215B1
Application number: EP95104015A
Authority: EP
Inventors: Eric J. Evain
Original assignee: Montell North America Inc
Current assignee: Basell North America Inc
Priority date: 1994-03-31
Filing date: 1995-03-18
Publication date: 1998-09-30
Anticipated expiration: 2015-03-18
Also published as: FI951556A; BR9501291A; JPH07278944A; CN1111294A; FI951556A0; ES2124927T3; RU95105024A; PH31402A; DE69505033T2; EP0675215A1; NO306911B1; CA2144934A1; ATE171733T1; CN1058063C; AU691569B2; NO951227D0; RU2139189C1; TR28851A; NO951227L; EG20572A

Abstract

A process for preparing thermal bondable fibers including exposing molten fiber grade polymer to electromagnetic radiation at the one or more orifices of the spinneret and the upper portion of the spin line, and the fibers prepared therefrom.

Description

This invention relates to a process of preparing fibers, in particular, an improved process of preparing thermal bondable fibers of fiber grade material.

Fibers of certain thermoplastic materials are used widely in the manufacturing of thermally bonded products, such as nonwoven textiles, by various processes. Said processes, such as calendering and spun bonding, require that the fibers have the capability of thermally bonding at temperatures lower than the melting point of the particular polymer(s) from which they are made, and that the fibers and articles manufactured therefrom be resistant to aging, yellowing and color variations caused by gas fading and oxidation.

There have been various attempts made to improve the thermal bondability of fibers, such as incorporating additives into the fiber grade polymer, elevating of spinning temperatures, forming fibers having two components and modifying the fiber surface. For example, U.S 4,473,677 to Pellegrini et al discloses adding a dianhydride of a 3,3',4,4' benzophenone tetracarboxylic acid or an alkyl derivative thereof to polyolefins to improve the thermal bonding of the fibers prepared therefrom. However, substantial problems are encountered during spinning at elevated temperatures and relatively slow spinning speeds are required.

Another approach is to add to the fiber grade polymer a low melting material, such as oligomers and waxes. The disadvantage of this approach is that the process must be modified to ensure adequate mixing of the materials so that gels are not formed in the fiber.

In the approach where fibers are formed from two different polymers, one component of the fiber has a lower melting point than the other, and covers the surface of the other component which has a higher melting point. These fibers are generally referred to as a "sheath-core" or "side-by-side" bicomponent fibers. The lower melting component enables thermal bonding at a temperature below the melting point of the fiber core.

Another approach is to modify the surface of the fiber once the fiber has been formed. Typically, these fibers contain only one fiber grade polymer, such as "skin fiber". Modification of the fiber surface can be obtained using various methods, such as irradiation, plasma treatment, ozone treatment, corona discharge treatment or chemical treatment.

In the typical process of melt spinning, the polymer is heated in an extruder to the melting point and the molten polymer is pumped at a constant rate under pressure through a spinneret containing one or more orifices of desired diameter, thereby producing filaments of the molten polymer. The molten polymer filaments are fed downward from the face of the spinneret into a cooling stream of gas, generally air. The filaments of molten polymer are solidified as a result of cooling to form fibers. Depending upon the spinning method used, the fibers are spread to form a fiber web and bonded directly, like in the spun bond method. Alternatively, in long spin methods, the fibers are gathered together and, if desired, drawn to orient the macromolecular structure of the fibers, and are then wound on bobbins. Bonding or calendering is then performed in a separate step. Generally, if there is any type of modification to be done to the filaments or fibers, such as surface modification carried out by chemical treatment or radiation treatment, the modification of the filaments or fibers takes place after the molten polymer filaments have solidified as a result of cooling to form the fiber, or on the preformed fiber itself.

It has now been found that the thermal bondability of fibers can be enhanced by treating the fiber grade polymer during the formation of the filaments, instead of treating the filaments or fibers after they are formed. The process of the present invention is not limited to any specific fiber preparation technique where a resin is melted and formed into a fiber, such as long spin, short spin, spun bond and melt blown fiber production methods. Nor is the spinning process limited to being carried out in any particular spinning environment, e.g. the presence or absence of oxygen or nitrogen.

Applicant has found that fibers having improved thermal bondability can be produced at lower spinning temperatures and increased spinning speeds by irradiating the molten fiber grade polymer filaments as soon as the filaments exit the orifices of the spinneret with electromagnetic radiation.

Accordingly, the present invention provides an improved process for the production of thermal bondable fibers comprising exposing the molten polymer filaments to from 1 x 10^-2 to 50 W/cm² of electromagnetic energy at the spinneret face.

Figure 1 is a schematic representation of a melt spinning arrangement used in the process of the present invention.

As used herein "spinneret face" is intended to include the upper portion of the spin line and the exit point of the molten material from one or more orifices, having any desired diameter, of the spinneret.

The phrase "fiber grade polymer" as used herein means any polymer that is capable of being spun into filaments to produce a fiber.

Referring to Figure 1, showing a typical melt-spinning apparatus, for use in preparing fibers according the invention, the fiber grade polymer is charged into a hopper 1, and fed into an extruder 2 of known or conventional type, containing single or multiple screws and equipped with controls for regulating the temperature of the barrel in various zones along the length of the barrel, where the polymer is heated to its melting point. The molten polymer is then fed to a metering pump 3, which delivers the molten polymer at a constant rate to a heated spinneret 4 containing one or more orifices. The fluid molten polymer filaments emerging in a downward direction from the face of the spinneret are exposed to electromagnetic radiation from a radiation source 5. The radiation source is positioned whereby the source encompasses the spinneret face. The molten polymer filaments are then solidified by cooling to form fibers 6.

The filaments produced by the process of this invention are typically combined into one or more fibers of varying thickness. Fibers made up of one filament are generally referred to as monofilament fibers and fibers made up of more than one filament are generally referred to as multifilament fibers. The spun denier of the fibers produced accordinq to the method of this invention range from less than 1.1 dtex to at least 55.6 dtex (1 to at least 50 dpf, denier) per filament. (Denier is the weight in grams of 9000 meters of fiber).

The fiber forming polymers useful in the present invention can be any polymer typically used to prepare fibers. Preferably, the fiber grade polymer is polyethylene, polypropylene, random copolymer of propylene and ethylene, polyisobutylene, polyamide, polyester, polystyrene, polyvinyl chloride, polyacrylate and mixtures thereof. Most preferred is polypropylene and random copolymers of propylene and ethylene.

In the process of the present invention the electromagnetic radiation can be ultraviolet, visible or infrared radiation. The total amount of electromagnetic energy that reaches the filament(s), referred to as irradiance, can be adjusted by changing the distance between the source of the radiation and the filament(s), changing the wavelength emitted by the source, and by changing the power, intensity, of the source. In the present invention, the total amount of electromagnetic energy that reaches the filament(s) is from 1 x 10^-2 to 50 M/cm² and from 1 x 10^-1 to 10 W/cm^2.

Conventional additives may be blended with the fiber forming polymer used to produce the thermal bondable fibers of the present invention. Such additives include, stabilizers, antioxidants, antislip agents, antistatic agents, flame retardants, nucleating agents, pigments, antisoiling agents, photosensitizers and the like.

The present invention will be illustrated in greater detail with reference to the examples of the invention set forth below.

Example 1

Fibers of Profax P-165 propylene homopolymer, stabilized with 100 ppm wt. Irganox 1010 tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane stabilizer, 1000 ppm wt. Irgafos 168 tris-(2,4-di-tert-butylphenyl)phosphite stabilizer and 1000 ppm wt. calcium stearate is prepared by charging the polymer composition into hopper, under a nitrogen blanket and fed into a single screw extruder, where the polymer composition is heated to its melting point. The molten polymer is fed to the meter pump, and pumped at a constant rate under pressure to a spinneret, containing one orifice with a diameter of 0.05cm (0.020 inches). The molten polymer filament emerging downward from the orifice of the spinneret is exposed to 0.88 W/cm² ultraviolet radiation. The filament of molten polymer is solidified as a result of cooling to form a monofilament fiber, and is collected on the godet. The processing conditions are as follows:

Extruder Feed Zone Temp.	220°C
Metering Pump Temp.	300°C
Spinneret Temp.	300°C
Fiber Spun Denier	2.2 dtex (2 g/9000 m)
Godet Take-up Speed	1000 m/min

The monofilament fibers prepared above were then tested for bond strength according to the following procedure. The fibers were cut into 400 mm lengths. The samples weighed between 0.160 and 0.170 grams. The fibers were then mechanically twisted eighty times and folded in half. The bundle was hand twisted six times and allowed to wrap around itself. The sample was bonded in a Sentinel Model 1212 heat sealer at 2.812 kg/cm² (40 psi) for 1.50 seconds at the desired temperature. The force required to separate the bonded segments (in grams) was recorded on an Instron Model 114 universal testing machine.

The results are set forth below in Table 1.

Comparative Example 1

Fibers were prepared according to the procedure of Example 1 using the same ingredients and processing conditions, except that the molten polymer filament emerging downward from the face of the spinneret was not exposed to the ultraviolet radiation.

The samples used to determine the bond strength were prepared and tested according to the method set for in Example 1.

The results of the thermal bonding are set forth below in Table 1.

	Bonding Temperatures
	135°C	140°C	145°C	150°C
Ex. 1	528 g	553 g	896 g	1650 g
Comp. Ex. 1	328 g	402 g	556 g	985 g

It can be seen that the bonding strength of the fibers of the present invention, even at the lower bonding temperature, is substantially higher than the bonding strength of the fibers of the Comparative Example 1 at the same bonding temperature.

Example 2

Fibers of propylene homopolymer having a MFR of 2.9 g/10 min., stabilized with Irganox 1076 octadecyl-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl) propanoate, 100 ppm wt. Irganox 1010 tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane stabilizer, 1000 ppm wt. Irgafos 168 tris(2,4-di-tert-butylphenyl)phosphite stabilizer and 1000 ppm wt. calcium stearate are prepared by according to the process of Example 1, except the processing conditions were as follows:

Extruder Feed Zone Temp.	220°C
Metering Pump Temp.	275°C
Spinneret Temp.	275°C
Fiber Spun Denier	9.9 dtex (9 g/9000 m)
Godet Take-up Speed	1000 m/min
Ultraviolet radiation	2.8 W/cm²

Comparative Example 2

Fibers were prepared according to the procedure of Example 2 using the same ingredients and processing conditions, except that the molten polymer filament emerging downward from the face of the spinneret was not exposed to the ultraviolet radiation.

The results of the thermal bonding are set forth below in Table 2.

	Bonding Temperatures
	130°C	140°C	145°C	150°C
Ex. 2	269 g	534 g	1033 g	1958 g
Comp. Ex. 2	160 g	236 g	271 g	492 g

The fibers of the present invention demonstrate better bonding strength as compared to the fibers of Comparative Example 2.

Example 3

Fibers of Profax P-165 propylene homopolymer stabilized with Irganox 1076 octadecyl-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl) propanoate, 100 ppm wt. Irganox 1010 tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane stabilizer, 1000 ppm wt. Irgafos 168 tris-(2,4-di-tert-butylphenyl)phosphite stabilizer and 1000 ppm wt. calcium stearate were prepared by according to the process of Example 1, except the processing conditions were as follows:

Extruder Feed Zone Temp.	220°C
Metering Pump Temp.	300°C
Spinneret Temp.	300°C
Fiber Spun Denier	2.2 dtex (2 g/9000 m)
Godet Take-up Speed	4000 m/min
Ultraviolet radiation	0.88 W/cm²

The samples used to determine the thermal bonding strength were prepared and tested according to the method set forth above in Example 1.

The results are set forth below in Table 3.

Comparative Example 3

Fibers were prepared according to the procedure of Example 4 using the same ingredients and processing conditions, except that the molten polymer filament emerging downward from the face of the spinneret was not exposed to the ultraviolet radiation.

The results of the thermal bonding are set forth below in Table 3.

	Bonding Temperatures
	135°C	140°C	145°C	150°C
Ex. 3	528 g	553 g	896 g	1650 g
Comp. Ex. 3	328 g	403 g	556 g	985 g

The fibers of the present invention demonstrate better bonding strength as compared to the fibers of Comparative Example 3.

Example 4

Fibers of Profax P-165 propylene homopolymer, stabilized with 100 ppm wt. Irganox 1010 tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane stabilizer, 1000 ppm wt. Irgafos 168 tris-(2,4-di-tert-butylphenyl)phosphite stabilizer and 1000 ppm wt. calcium stearate were prepared by according to the process of Example 1, except the processing conditions were as follows:

Extruder Feed Zone Temp.	220°C
Metering Pump Temp.	250°C
Spinneret Temp.	250°C
Fiber Spun Denier	2.2 dtex (2 g/9000 m)
Godet Take-up Speed	2250 m/min
Ultraviolet radiation	0.88 W/cm²

The results are set forth below in Table 4.

Comparative Example 4

The results are set forth below in Table 4.

	Bonding Temperatures
	130°C	140°C	145°C
Ex. 4	196 g	341 g	533 g
Comp. Ex. 4	132 g	291 g	350 g

The fibers of the present invention demonstrate better bonding strength as compared to the fibers of Comparative Example 4.

The thermal bondable fibers prepared according to the process of the present invention can be used in the manufacturing of nonwovens, by spun bonded and melt blown processes. Nonwovens are useful in the production of personal hygiene products, for example, infant care and adult incontinence products, protective covering, for example surgical gowns and shoe covers and other disposable medical and clothing products.

Claims

A process for preparing a thermal bondable fiber, comprising

i) extruding molten polymer through a spinneret (4) having a spinneret face containing at least one orifice through which a fluid molten polymer filament emerges,

ii) exposing said molten polymer filament to an electromagnetic energy of from 1 x 10^-2 to 50 W/cm², and

iii) solidifying said molten polymer filament to form a fiber (6).
The process of claim 1, comprising

i) extruding a molten polymer through a spinnert (4) having a spinneret face containing a plurality of orifices to form a plurality of molten polymer filaments,

ii) exposing said molten polymer filaments to an electromagnetic energy of from 1 x 10^-2 to 50 W/cm², and

iii) solidifying said molten polymer filaments to form thermal bondable fibers (6).
The process of claim 1, wherein said filament emerges from the spinneret face in a downward direction.
The process of claim 1, wherein said thermal bondable fiber (6) comprises a polymer selected from the group consisting of polyethylene, polypropylene, random copolymer of propylene and ethylene, polyisobutylene, polyamide, polyester, polystyrene, polyvinyl chloride, polyacrylate and mixtures thereof.
The process of claim 1, wherein the source of said electromagnetic energy (5) is selected from ultraviolet radiation, visible radiation and infrared radiation.
The process of claim 5, wherein said source is ultraviolet radiation.
The process of claim 1, wherein the energy is from 1 x 10^-1 to 10 W/cm².
A thermal bondable fiber prepared according to the process of claim 1.