Buffer Layer for Strings

Yaniv; Zvi ;   et al.

Patent Application Summary

U.S. patent application number 11/940976 was filed with the patent office on 2008-05-29 for buffer layer for strings. This patent application is currently assigned to NANO-PROPRIETARY, INC.. Invention is credited to Yunjun Li, Dongsheng Mao, Zvi Yaniv.

Application Number20080124546 11/940976
Document ID /
Family ID39186839
Filed Date2008-05-29

United States Patent Application 20080124546
Kind Code A1
Yaniv; Zvi ;   et al. May 29, 2008

Buffer Layer for Strings

Abstract

A thin buffer layer is used to coat on the multi-filament wrapped string to fill the gaps. The polymers of the buffer-layer coating have a high melt-flow (low viscosity) during coating process to fill all the gaps between the filaments, and the filaments are fixed by the coatings onto base core materials.


Inventors: Yaniv; Zvi; (Austin, TX) ; Li; Yunjun; (Austin, TX) ; Mao; Dongsheng; (Austin, TX)
Correspondence Address:
    FISH & RICHARDSON P.C.
    P.O BOX 1022
    Minneapolis
    MN
    55440-1022
    US
Assignee: NANO-PROPRIETARY, INC.
Austin
TX

Family ID: 39186839
Appl. No.: 11/940976
Filed: November 15, 2007

Related U.S. Patent Documents

Application Number Filing Date Patent Number
60866199 Nov 16, 2006

Current U.S. Class: 428/377 ; 427/206
Current CPC Class: D07B 1/165 20130101; D07B 2205/3007 20130101; D07B 2201/2074 20130101; D07B 2205/10 20130101; D07B 2201/1036 20130101; D07B 2201/2087 20130101; D07B 2205/3007 20130101; D07B 1/02 20130101; D07B 2205/2046 20130101; D07B 2205/2046 20130101; D07B 2801/20 20130101; D07B 2801/22 20130101; D07B 2801/16 20130101; D07B 2801/22 20130101; D07B 2205/10 20130101; D07B 1/162 20130101; Y10T 428/2936 20150115; A63B 51/02 20130101; G10D 3/10 20130101
Class at Publication: 428/377 ; 427/206
International Class: D02G 3/00 20060101 D02G003/00

Claims



1. A coating for a string, comprising: a core filament wrapped with a plurality of wrapping filaments of a smaller diameter than the core filament; a buffer layer coating filling in gaps between the wrapping filaments and between the wrapping filaments and the core filament; and an outer coating covering over the buffer layer coating, wrapping filaments and core filament.

2. The coating of claim 1, wherein the buffer layer coating comprises a polymer.

3. The coating of claim 1, wherein the buffer layer coating comprises nylon.

4. The coating of claim 3, wherein the buffer layer coating comprises nylon 6.

5. The coating of claim 3, wherein the buffer layer coating comprises nylon 11.

6. The coating of claim 3, wherein the outer coating comprises a composite of nylon and clay nanoparticles.

7. The coating of claim 3, wherein the outer coating comprises a composite of nylon and carbon nanotubes.

8. The coating of claim 6, wherein the outer coating further comprises a modifier.

9. A method for coating a string comprising: wrapping a core filament having a first diameter with one or more wrapping filaments having a second diameter that is less than the first diameter; extruding a melted nylon into gaps between the one or more wrapping filaments and into gaps between the wrapping filaments and the core filament; extruding a coating on a circumference of the string so that it covers the one or more wrapping filaments and the melted nylon in the gaps.

10. The method of claim 9, wherein the melted nylon comprises nylon 6.

11. The method of claim 9, wherein the melted nylon comprises nylon 11.

12. The method of claim 9, wherein the coating comprises a composite of nylon and clay nanoparticles.

13. The method of claim 9, wherein the coating comprises a composite of nylon and carbon nanotubes.

14. The method of claim 9, wherein the coating comprises a composite of nylon and ceramic particles.

15. The method of claim 9, wherein the coating comprises a composite of nylon and glass particles.

16. The method of claim 9, wherein the coating is between 1 and 100 micrometers thick.

17. The coating of claim 1, further comprising: another plurality of wrapping filaments wrapped around the outer coating; another buffer layer coating filling in gaps between the another plurality of wrapping filaments; and another outer coating covering over the another buffer layer coating.

18. The coating of claim 3, wherein the coating comprises a composite of nylon and glass particles.

19. The coating of claim 3, wherein the coating comprises a composite of nylon and ceramic particles.
Description



[0001] This application claims priority to U.S. Provisional Application Ser. No. 60/866,199, which is hereby incorporated by reference hereby.

BACKGROUND

[0002] The strings for sports equipment (e.g., tennis raquets) or musical instruments are usually coated with a thin layer at their outmost surface to improve their durability, spin, feeling, etc. Polyamide (nylon), polyester, and other polymers have been used to coat on strings. Nanocomposites, such as clay and carbon nanotube reinforced nylon 6 nanocomposites, having better physical properties than neat nylon 6, are of a potential to be highly durable string coating materials with other functionalities. The reinforcing polymeric composites using nano-sized clay particles with high aspect ratio have been investigated since the 1980's (see U.S. Pat. No. 4,739,007). Strings are usually polymer materials with a multi-layer structure--core filament, wrapping filaments on the core filament, and coating. For the strings with multi-layer structures, coating materials are required to match the base materials and have good melt-flow properties (acceptable viscosity) at certain temperature to allow them to be penetrated into the gaps between the wrapping filaments. Viscosity of a nanocomposite is usually higher than neat nylon 6 at the same temperature. Thus, the nanocomposite may not easily penetrate into the gaps between the wrapping filaments. FIG. 1 shows an SEM image of a cross-section view of a nylon 6/clay nanocomposite coated on a wrapping filament. It can be seen that the nanocomposite material did not successfully fill out the gaps. Many defects were left in the string which will result in unacceptable durability of the strings. The gaps will result in chipping-off or unacceptable durability of coatings during high impact hitting of balls. More over, due to creation of the gaps, coatings also fail to a fix the filaments on the core materials of the string. FIG. 2 shows the chipped materials from filaments and coatings after high impact tests on the strings.

BRIEF DESCRIPTION OF THE DRAWINGS

[0003] FIG. 1 shows an SEM image of a cross-section view of a nylon 6/clay nanocomposite coated on a wrapping filament;

[0004] FIG. 2 shows an SEM image of chipped materials from filaments and coatings after high impact tests on a string;

[0005] FIG. 3A illustrates a cross-section of a core filament with wrapping filaments surrounding it;

[0006] FIG. 3B illustrates a buffer layer applied onto the wrapping filament;

[0007] FIG. 3C illustrates a coating applied onto the buffer layer; and

[0008] FIG. 4 illustrates another embodiment of the present invention.

DETAILED DESCRIPTION

[0009] Although polymer nanocomposites have higher physical/mechanical properties than neat polymer materials, they normally have higher viscosity or melt-flow during an extrusion or coating process. To solve this problem, a thin buffer layer is used to coat on the multi-filament wrapped string to fill the gaps. The polymers of the buffer-layer coating have a high melt-flow (low viscosity) during coating process to fill all the gaps between the filaments, and the filaments are fixed by the coatings onto base core materials.

Example 1

A Coating System with a Nylon 6 Buffer Layer

[0010] FIG. 3A illustrates a cross-section of a string for coating comprised of one monofilament core 301 wrapped with smaller-diameter multi-filaments 302. Neat nylon 6 pellets as may be obtained from UBE Industries Inc. (product name: UBE SF 1018 A) are melted. The buffer layer coating 303 is applied by an extrusion process at temperatures ranging from 220.degree. C. to 270.degree. C. The thickness of the buffer layer 303 may be from 10 to 100 micrometers. The gaps between the multi-filaments 302 are fully filled by the neat nylon 6 coating.

[0011] A wear-resistant coating 304 is then coated (FIG. 3C) by an extrusion process at temperatures ranging from 240.degree. C. to 280.degree. C. A nylon 6/clay or nylon 6/carbon nanotube nanocomposite may be employed as the wear-resistant coating material 304. The nylon 6 nanocomposite produced by in-situ polymerization may contain 4% nano-clay filler. Other nylon 6 nanocomposites produced by melt-compounded process may also be used for the wear-resistant coatings 304. Except for the clay, carbon nanotubes, ceramic particles such as SiO.sub.2 and Al.sub.2O.sub.3, or glass particles may be used to make nylon 6 nanocomposites. The Nylon 6 nanocomposites may also be modified by rubber modifiers to improve the ductility and toughness. The thickness of the wear-resistant coating may be from 1 to 100 micrometers.

Example 2

A Coating System with a Nylon 11 Buffer Layer

[0012] Again referring to FIG. 3A, the string for coating is one monofilament core 301 wrapped with smaller-diameter multi-filaments 302. Neat nylon 11 may be obtained from ARKEMA Inc. Nylon 11 has a very good melt flow at temperatures over 220.degree. C. Good impact strength and shear strength also make nylon 11 a good buffer layer material. In FIG. 3B, the buffer layer coating 303 is applied by an extrusion process at temperatures ranging from 190.degree. C. to 270.degree. C.

[0013] The thickness of the buffer layer 303 may be from 10 to 100 micrometers. The gaps between the multi-filaments 302 are fully filled by the neat nylon 11 coating.

[0014] Referring to FIG. 3C, a wear-resistant coating 304 is then coated by an extrusion process at temperatures ranging from 240.degree. C. to 280.degree. C. Nylon 6/clay or a nylon 6/carbon nanotube nanocomposite may be employed as the wear-resistant coating material 304. The nylon 6 nanocomposite produced by in-situ polymerization may contain 4% nano-clay filler. Other nylon 6 nanocomposites produced by melt-compounded process may also be used for the wear-resistant coating 304. The nylon 6 nanocomposites may also be modified by rubber modifiers to improve the ductility and toughness. The thickness of the wear-resistant coating 304 may be from 1 to 100 micrometers.

[0015] Except for the extrusion process to deposit a coating on the string, other methods such as spraying, dipping, spin coating, brushing, painting, and immersing processes can be used to deposit a coating on the surface of strings. Nylon 6 nanocomposites may be melted at higher than 190.degree. C. and extruded to deposit a coating on the strings. Nylon 6 nanocomposites may be dissolved in a solvent such as formic acid and sprayed, dipped, spin coated, brushed, painted, or immersed to deposit a coating on the string at room temperature or elevated temperatures. The solvent may be then removed by a follow-up process such as an evaporation method.

[0016] FIG. 4 illustrates another embodiment of the present invention. Essentially, the coated string structure of FIG. 3C is then coated again with smaller-diameter multi-filaments 401. A buffer layer coating 402, similar to layer 303, is applied by an extrusion process at temperatures ranging from 190.degree. C. to 270.degree. C. The thickness of the buffer layer 402 may be from 10 to 100 micrometers. The gaps between the multi-filaments 401 are fully filled by the neat nylon 11 coating. A wear-resistant coating 403 is then coated by an extrusion process at temperatures ranging from 240.degree. C. to 280.degree. C. Nylon 6/clay or a nylon 6/carbon nanotube nanocomposite may be employed as the wear-resistant coating material 403. The nylon 6 nanocomposite produced by in-situ polymerization may contain 4% nano-clay filler. Other nylon 6 nanocomposites produced by melt-compounded process may also be used for the wear-resistant coating 403. The nylon 6 nanocomposites may also be modified by rubber modifiers to improve the ductility and toughness. The thickness of the wear-resistant coating 403 may be from 1 to 100 micrometers.

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