Elastic nonwoven materials comprising propylene-based and ethylene-based polymers
A polymer and non-woven technology, which is applied in the field of elastic non-woven materials and non-woven materials, can solve the problems of increasing cost, extra volume or weight, low crystallinity of elastomers, and difficulty in processing elastomers.
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[0050] Preparation of Propylene-Based Polymers
[0051] Polymerization of the propylene-based polymer can be carried out by reacting the monomers in the presence of the catalyst system described herein at a temperature of 0°C to 200°C for a period of 1 second to 10 hours. Preference is given to using homogeneous conditions, such as continuous solution processes or bulk polymerization processes with excess monomers used as diluents. Continuous processes may use some form of agitation to reduce concentration differences in the reactor and maintain steady state polymerization conditions. The heat of polymerization is preferably removed by cooling the polymerization feed and allowing the polymerization to heat up to polymerization, although an internal cooling system may be used.
[0052] Further descriptions of exemplary processes suitable for preparing the propylene-based polymers described herein can be found in US Patent No. 6,881,800, incorporated herein by reference in acco...
Embodiment 1
[0125] Using standard commercial fiber spinning equipment with a throughput of 0.4 grams per hole per minute (ghm), the present invention consists of 85 wt% PBP1 (visbroken to an MFR of about 40 g / 10min) and 15 wt% EPB1 The blend formed a partially oriented yarn (72 filaments). The fibers were drawn at 1500 m / min. Comparative fibers were also prepared from PBP2 using the same equipment and method. The results of the first and second cycle hysteresis for the blends of the invention are as follows Figure 1a shown and compared materials such as Figure 1b shown.
[0126] like Figure 1a and 1b As shown in , the addition of ethylene-based polymers provides a favorable balance of better elasticity and processability compared to the use of polypropylene as a blending partner (as in Figure 1b among the comparative polymers shown in). This is done with Figure 1b When comparing, Figure 1a Evidenced by the significantly reduced area within the hysteresis curves of the blends. ...
Embodiment 2
[0128] Partially oriented yarns were spun from a comparative polymer blend and two inventive polymer blends using the same equipment and method as in Example 1 . A comparative polymer blend comprised 85% by weight of PBP1 and 15% by weight of a propylene homopolymer having an MFR of about 35 g / 10min. The first and second cycle hysteresis loops of the comparative blends are as Figure 2a shown in . The first inventive polymer blend comprised 85% by weight of PBP1 and 15% by weight of EBP2. The first and second cyclic hysteresis loops of the first inventive blend are as follows Figure 2b shown. The second inventive polymer blend comprised 87.4% by weight of PBP1, 5.5% by weight of EBP1 and 7.1% by weight of EBP3. The first and second cycle hysteresis loops for the second inventive blend are shown in Figure 2c. In all cases, PBP1 was first visbroken to an MFR of about 40 g / 10 min before blending with the specified blending partners.
[0129] Figure 3a , 3b and 3c are re...
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