Patent Application
20060111487
The present invention relates to hydrolysis resistant polyamide compositions having good flexibility, and various articles including tubular structures such as pipes and the like that may be made from these polyamide compositions.
Due to their good physical properties and chemical resistance, various polyamides find many applications as engineering polymers. Such applications often require that the polyamide be in contact with water, and many applications require elevated temperatures. Examples include an undersea oil pipe that comes into contact with hot oil from the earth's interior and automobile radiator tubing. Under such conditions, the amide bonds of many polyamides may be susceptible to hydrolysis in the presence of water and the rate of hydrolysis increases with temperature. Hydrolysis of the amide bonds can cause a reduction in molecular weight and concomitant loss in physical properties that can result in failure of the pipe during use. Such a failure can be catastrophic, with the loss of fluid causing undesirable consequences ranging from the impairment of the performance of the device within which the piping is incorporated, to contact of the fluid with the surrounding environment.
Aliphatic polyamides such as polyamide 6,12 or polyamide 11 are frequently used to make pipes and other tubular structures, but many applications require greater hydrolysis resistance than can be obtained from currently available polyamides.
It would be desirable to obtain a polyamide having both good hydrolysis resistance and that could be conveniently plasticized to be useful in manufacturing pipes. A further object of the present invention is to provide piping, tubing and the like which is readily prepared from the instant compositions of the present invention as by conventional means well accepted in the field. A feature of the present invention is that the instant compositions are formable into any of a wide variety of structural designs and configurations. An advantage of the present invention is that these structural components can be further optimized for specialized functions with the addition of an assortment of additives including stabilizers, colorants, molding agents, and the like. These and other objects, features and advantages of the invention will become better understood upon having reference to the following description of the invention.
There is disclosed and claimed herein polyamide compositions comprising a polyamide comprising;
There is further disclosed and claimed herein a variety of articles of manufacture made from the instant composition, including without limitation tubular structures such as tubing and piping.
There are a number of terms used throughout the specification for which the following will be of assistance in understanding their scope and meaning. As used herein and as will be understood by those skilled in the art, the terms “terephthalic acid”, “isophthalic acid”, and “dicarboxylic acid/dioic acid” refer also to the corresponding carboxylic acid derivatives of these materials, which can include carboxylic acid esters, diesters, and acid chlorides. Moreover and as used herein, and as will be understood by one skilled in the art, the term “hydrolysis resistant” in conjunction with a polyamide refers to the ability of the polyamide to retain its molecular weight upon exposure to water.
As used herein, the term “tubular structure” includes without limitation a variety of shapes such as “pipes”, “tubing” and the like and refers to various bodies defining a cavity therethrough for conducting a fluid including without limitation any liquid, gas, or finely divided solid. These tubular structures (pipes and the like) may be flexible or stiff and have a variety of wall thicknesses and (in the event such pipes are circular in cross section) diameters. These pipes and the like may have a circular or roughly circular (e.g. oval) cross-section. However more generally such pipes and the like may be shaped into seemingly limitless geometries so long as they define a passageway therethrough. For example suitable shapes may include polygonal shapes and may even incorporate more that one shape along the length thereof. Such tubular structures may further be joined together by suitable means to form T-sections, branches, and the like. Moreover, tubular structures may comprise multiple concentric layers, wherein at least one layer comprises a polyamide composition. Other layers may comprise other polymeric materials or metals.
For convenience of description only, the term “pipe” is used most regularly throughout the specification, although those having skill in the art will readily understand that such references also contemplate other shapes as described above.
The polyamide composition of the present invention comprises a polyamide comprising about 3 to about 14 mole percent, or preferably about 4 to about 12 mole percent, or more preferably about 5 to about 10 mole percent of repeat units (a) that are derived from at least one aromatic dicarboxylic acid having 8 to 16 carbon atoms and/or at least one alicyclic dicarboxylic acid having 8 to 20 carbon atoms and at least one aliphatic diamine having 4 to 20 carbon atoms. The polyamide further comprises about 86 to about 97 mole percent, or preferably about 88 to about 96 mole percent, or more preferably about 90 to about 95 mole percent of repeat units (b) that are derived from monomers selected from the group consisting of: (i) two or more aliphatic dicarboxylic acids having 6 to 36 carbon atoms and at least one aliphatic diamine having 4 to 20 carbon atoms; (ii) two or more aliphatic diamines having 4 to 20 carbon atoms and at least one aliphatic dicarboxylic acid having 6 to 36 carbon atoms; (iii) at least one aliphatic dicarboxylic acid having 6 to 36 carbon atoms and at least one aliphatic diamine having 4 to 20 carbon atoms and at least one lactam or aminocarboxylic acid having 4 to 20 carbon atoms; and (iv) at least two monomers selected from lactams and aminocarboxylic acids having 4 to 20 carbon atoms.
By “aromatic dicarboxylic acid” is meant dicarboxylic acids in which each carboxyl group is directly bonded to an aromatic ring. Examples of suitable aromatic dicarboxylic acids include terephthalic acid; isophthalic acid; 1,5-nathphalenedicarboxylic acid; 2,6-nathphalenedicarboxylic acid; and 2,7-nathphalenedicarboxylic acid. Terephthalic acid and isophthalic acid are preferred. By “alicyclic dicarboxylic acid” is meant dicarboxylic acids in which each carboxyl group is directly bonded to a saturated hydrocarbon ring. An example of a suitable alicyclic dicarboxylic acids includes 1,4-cyclohexanedicarboylic acid.
Examples of aliphatic dicarboxylic acids having 6 to 36 carbon atoms include adipic acid, nonanedioic acid, decanedioic acid (also known as sebacic acid), undecanedioic acid, dodecanedioic acid, tridecanedioic acid, and tetradecanedioic acid. The aliphatic diamines having 4 to 20 carbon atoms may be linear or branched. Examples of preferred diamines include hexamethylenediamine, 2-methylpentamethylenediamine; 1,8-diaminooctane; methyl-1,8-diaminooctane; 1,9-diaminononane; 1,10-diaminodecane; and 1,12-diaminedodecane. Examples of lactams include caprolactam and laurolactam. An example of an aminocarboxylic acid includes aminodecanoic acid.
Preferred polyamides are semiaromatic polyamides. The polyamides preferably comprise repeat units (a) that are derived from terephthalic acid and/or isophthalic acid and hexamethylenediamine and repeats units (b) that are derived from two or more of nonanedioic acid and hexamethylenediamine; decanedioic acid and hexamethylenediamine; undecanedioic acid and hexamethylenediamine; dodecanedioic acid and hexamethylenediamine; tridecanedioic acid and hexamethylenediamine; tetradecanedioic acid and hexamethylenediamine; laurolactam; and 11-aminoundecanoic acid.
A preferred polyamide comprises repeat units (a) that are derived from terephthalic acid and hexamethylenediamine and repeat units (b) that are derived from decanedioic acid, dodecanedioic acid, and hexamethylenediamine. The ratio of repeat units (b) derived from decanedioic acid and hexamethylenediamine to repeat units (b) derived from dodecanedioic acid and hexamethylenediamine is preferably between about 19:1 and 1:19, or more preferably between about 4:1 and 1:4.
The polyamide of the present invention may be prepared by any means known to those skilled in the art, such as in an batch process using, for example, an autoclave or using a continuous process. See, for example, Kohan, M. I. Ed. Nylon Plastics Handbook, Hanser: Munich, 1995; pp. 13-32. Additives such as lubricants, antifoaming agents, and end-capping agents may be added to the polymerization mixture.
The polyamide composition of the present invention may optionally comprise additives. A preferred additive is at least one plasticizer. The plasticizer will preferably be miscible with the polyamide. Examples of suitable plasticizers include sulfonamides, preferably aromatic sulfonamides such as benzenesulfonamides and toluenesulfonamides. Examples of suitable sulfonamides include N-alkyl benzenesulfonamides and toluenesufonamides, such as N-butylbenzenesulfonamide, N-(2-hydroxypropyl)benzenesulfonamide, N-ethyl-o-toluenesulfonamide, N-ethyl-p-toluenesulfonamide, o-toluenesulfonamide, p-toluenesulfonamide, and the like. Preferred are N-butylbenzenesulfonamide, N-ethyl-o-toluenesulfonamide, and N-ethyl-p-toluenesulfonamide.
The plasticizer may be incorporated into the composition by melt-blending the polymer with plasticizer and, optionally, other ingredients, or during polymerization. If the plasticizer is incorporated during polymerization, the polyamide monomers are blended with one or more plasticizers prior to starting the polymerization cycle and the blend is introduced to the polymerization reactor. Alternatively, the plasticizer can be added to the reactor during the polymerization cycle.
When used, the plasticizer will be present in the composition in about 1 to about 20 weight percent, or more preferably in about 6 to about 18 weight percent, or yet more preferably in about 8 to about 15 weight percent, wherein the weight percentages are based on the total weight of the composition.
The polyamide composition may optionally comprise additional additives such as thermal, oxidative, and/or light stabilizers; colorants; lubricants; mold release agents; and the like. Such additives can be added in conventional amounts according to the desired properties of the resulting material, and the control of these amounts versus the desired properties is within the knowledge of the skilled artisan.
When present, additives may be incorporated into the polyamide composition of the present invention by melt-blending using any known methods. The component materials may be mixed to homogeneity using a melt-mixer such as a single or twin-screw extruder, blender, kneader, Banbury mixer, etc. to give a polyamide composition. Or, part of the materials may be mixed in a melt-mixer, and the rest of the materials may then be added and further melt-mixed until homogeneous.
The polyamide composition of the present invention may be formed into shaped articles using any suitable melt-processing technique, such as injection molding, extrusion, blow molding, injection blow molding, thermoforming and the like.
Preferred articles include tubular structures such as pipes and tubes. Examples of preferred tubular structures include, but are not limited to, tubing for use in vehicle radiators; flexible pipe, including undersea flexible oil pipes; above sea oil pipes; in-ground oil pipes; pipe liners; and components of marine umbilicals. Flexible pipes are described in U.S. Pat. No. 6,053,213, which is hereby incorporated herein by reference. The pipes may be formed such they comprise multiple layers, wherein one of the layers comprises the polyamide composition of the present invention.
This application claims the benefit of U.S. Provisional Application No. 60/622,513, filed Oct. 27, 2004.
| Number | Date | Country | |
|---|---|---|---|
| 60622513 | Oct 2004 | US |
