Nylon compositions

Abstract

A polyamide includes a plurality of amide units forming a polymer chain, and an alkyl substituent on the amide group. The polyamide has a substitution of the amide units in an amount of between about 0.1% to about 10% of the amide units in the polymer chain, and the polyamide comprises one or more additives.

Description

NYLON COMPOSITIONSCROSS-REFERENCE TO RELATED APPLICATIONS

[0001] The present application claims priority to U.S. Provisional Patent Application No. 63 / 519,793 filed on August 15, 2023 and entitled, ‘‘Nylon Compositions”, the entirety of which is incorporated herein by reference.BACKGROUND

[0002] Nylon can be produced by the polymerization of amide units, and the type of nylon produced can be referred to by the number of carbon atoms in the monomer unit being polymerized. Nylon may be less stable than other types of polymers (e.g., polyethylene) due to the presence of the amide units. The instability can include thermal instabilities that can make processing of the nylon difficult.SUMMARY

[0003] In some embodiments, a polyamide comprises a plurality of amide units forming a polymer chain, and an alkyl substituent on the amide group. The polyamide has a substitution of the amide units in an amount of between about 0.1% to about 10% of the amide units in the polymer chain, and the polyamide comprises one or more additives.

[0004] In some embodiments, a method of forming a polyamide composition comprises providing a polyamide that comprises a plurality of amide groups in a backbone structure of the polyamide, modifying a portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents to form the polyamide composition, and incorporating one or more additives into the polyamide. The polyamide has a substitution of the amide units in an amount of betw een about 0.1% to about 10% of the amide units in the backbone.

[0005] These and other features will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings and claims.DETAILED DESCRIPTION

[0006] Various Nylons or polyamides can be modified to provide useful polymers. For example, poly-2-pyrrolidone can be produced by the alkaline-catalyzed polymerization of 2-pyrrolidone in the presence of various compounds such as carbon dioxide. The resulting polymer can be referred to in some contexts as Nylon 4 based on the polymerization of monomer contain 4 carbon atoms. Additional modifications can be used to alter the properties (e.g., melting temperature, degradation temperature, molecular weight, functionalization, etc.) of thepolypyrrolidone, and the resulting material can show improved biodegradation relative to other polymers such as olefin-based polymers including polyethylene, polypropylene, and the like. To the extent that articles can be formed from degradable materials, the environmental persistence of such polymers can be reduced relative to other polymers.

[0007] The resulting polypyrrolidone can be formed into various forms and products to allow for a variety of end uses including sheets, films, filaments, ribbons, molded articles, and fibers. Because of its hydrophilic properties, which closely resemble those of cotton and silk, polypyrrolidone fiber has long been recognized as having great commercial potential. For example, fabrics made from polypyrrolidone, in contrast with other presently available synthetic fibers, are as readily dyed as cotton, they may be ironed at cotton temperatures, they rapidly dissipate static charges, and, in particular, they possess the comfort of cotton, silk, and wool.

[0008] The biodegradability is balanced with the ability to form useful articles from the polymers. To form filaments and fibers, the polymer can be melt-spun into filaments by extrusion from spinnerets. In melt-spinning, the polymer composition is extruded in a molten condition at a melt temperature which is generally between about 230°C to about 280°C, or between about 245°C to about 270°C, or in some instances greater than about 270°C. This extrusion must be carried out with care because of the thermal degradation of the polymer, which can cause the polymer to revert back to monomer. As well as causing substantial product loss and increasing process cost, this can also cause bubbles and the formation of voids or pox marks in the extrudate or filaments. Moreover, in addition to monomer reversion, molecular weight degradation also occurs during melt spinning resulting in poly-2-pyrrolidone filaments having substantially lower molecular weights than the original polymer. If the molecular weight of the initial polymer is too low or if the molecular weight degradation is too severe, the molecular weight of the filaments will be inadequate to afford the filaments sufficient tensile strength and fibrillation properties.

[0009] In addition to melt-spinning, solution-spinning is a method for the formation of useful articles from the polymer. If solution spinning is used the polymer is dissolved in a solvent to a high concentration, commonly called a dope, and then extruded into a non-solvent where precipitation occurs and the articles are formed. Typical concentrations for dope solutions can be between 2.5 wt% - 50 wt%, resulting in high-viscosity solutions of the range of 1000 centipoise to 1,000,000 centipoise or higher, most preferably 5000 centipoise to 50,000 centipoise. Examples of solvents that can be used are acids, polar protic, polar aprotic, ionic liquids, fluorinated alcohols and the like.

[0010] A further problem is that higher molecular weight (e.g., about 120,000 and above) polymers, although thermally more stable, are also more viscous and more difficult to extrude. If extrusion is attempted at appreciably lower temperatures to avoid thermal decomposition, the material is not properly melted and fibers of substantially lower tensile strength are produced. Consequently, in order to melt extrude polypyrrolidone efficiently, the thermal stability- of the polymer and / or to the extrudability of the polymeric composition can be improved.

[0011] In some aspects, a polypyrrolidone is disclosed herein that allows for the melting temperature to be lowered and / or the thermal stability- to be increased, thereby improving the workability of the polymers. In some aspects, the disclosed methods and resulting polymers allow for the lowering of the melting point of the resulting polymer while not affecting the degradation temperature. Alternatively, raising the degradation temperature of the resulting polymer while not affecting the melting point is also possible. This can then allow the polymer to be more easily worked and formed into useful articles without degrading the polymer in the process.

[0012] This disclosure relates to various polyamide compositions that can be modified to improve the processability while maintaining a bio-degradability-. While various nylons can be produced as provided herein, in some aspects a poly-2-pyrrolidone compositions that are modified to have improved thermal stabilities and to methods of treating poly-2-pyrrolidone to prepare the modified poly-2 pyrrolidone compositions are described as examples. Other polyamides such as Nylon 3, Nylon 4, Nylon 6, proteins, and other classes of nylons such as Nylon 2,2, Nylon 3,3, and the like can be similarly modified as provided herein to improve the properties including lowering the melting point and / or raising the degradation temperature. In general, the modification techniques described herein can be used on any suitable polyamide.

[0013] 2-pyrrolidone can be polymerized to form the poly-2-pyrrolidone using any suitable techniques. Methods for the polymerization of 2-pyrrolidone to form poly-2-pyrrolidone, which can also simply be referred to as polypyrrolidone herein, can include the polymerization of 2- pyrrolidone in the presence of an alkaline polymerization catalyst, if desired with an activator. Cationic ring opening polymerization methods can also be used.

[0014] The polymer formed from 2-pyrrolidone is believed to be a linear polyamide, which has come to be known as nylon-4, having the structure:Formula 1 where n can range from about 200 to over 1,000,000, or in some aspects as high as 100,000. In some aspects, n may range as high as about 10,000, or about 5000 depending on the type of nylon considered. A more general formulation of a nylon formed from a generic starting material can include:Formula 2 where when m is 1, the polyamide is nylon 2, when m is 2, the polyamide is nylon 3, when m is 3 the polyamide is nylon 4, n can be any of the values noted above for Formula 1, and R can by hydrogen or another alkyl modification as provided herein.

[0015] In some aspects, the poly pyrrolidone can be prepared by polymerizing 2-pyrrolidone using an alkaline polymerization catalyst in the presence of carbon dioxide (CO2). For example, polymerization can be effected by bubbling CO2 through a mixture of 2-pyrrolidone and an alkali metal salt of 2-pyrrolidone, e.g., sodium or potassium pyrrolidonate, the alkali metal pyrrolidonate functioning as an alkaline polymerization catalyst. The polypyrrolidone can also be prepared by reacting CO2 with the alkali metal salt of 2-pyrrolidone to form an adduct of CO2 and the alkali metal pyrrolidonate, and then polymerizing the 2-pyrrolidone monomer in the presence of the adduct.

[0016] In some aspects, the polymerization of 2-pyrrolidone can be carried out using an alkaline polymerization catalyst in the presence of CO2. The 2- pyrrolidone monomer may be polymerized at a temperature from 18°C to about I00°C, preferably 25 °C to 70°C, and most preferably 25°C to 60°C, under a pressure ranging from subatmospheric to superatmospheric in the presence of the alkaline polymerization catalyst. Bulk polymerization or suspension polymerization can be used.

[0017] The alkaline polymerization catalyst can be any of those used in polymerizing 2- pyrrolidone. Suitable alkaline polymerization catalysts are derivatives of the alkali metals, e.g. the hydroxides and oxides of the alkali metals, including potassium tert-butoxide. The alcoholates of the alkali metals, such as sodium methylate, may also be used. In addition, the oxides and hydroxides of the alkaline earth metals, for example, calcium and barium, may be used as catalysts. Also, organic metallic compounds, preferably those which are strongly basic,may be used, such as lithium, potassium and sodium alkyls, e g. butyl lithium, and the ary ls of the alkali metals, such as sodium phenyl and sodium amide. The alkaline polymerization catalyst may be a quaternary ammonium base. Still further, as previously mentioned, the catalyst may be an alkali metal hydride, such as sodium hydride. While certain alkali metal derivatives can be used, many of them are undesirable. For example, the alkali metal carbonates as well as the alkaline earth metal hydroxides tend to be insoluble and for this reason are undesirable. Lithium hydroxide (monohydrate) also is insoluble in 2-pyrrolidone.

[0018] In some aspects, a non-ionic base can also be used as a catalyst. For example, the polymerization can be catalyzed by strong, nitrogen- and phosphorous-containing non-ionic bases. The catalysts or initiators which are effective may include non-ionic bases with a pKa of equal to or greater than 30. Examples of non-ionic bases which are useful can include poly aminophosphazenes, including phosphazene bases of the structure:where R1is (Ci -Cx) alkyl wherein when alky l is greater than C3 it is branched or linear, and R is Me or both R’s together are -(CH2)4 and m, n, and y are independently 0-3 or preferably as defined below for the specific phosphazene Px (x=l to 7) bases. Preferred R1groups include t- butyl, t-heptyl (-C(CH3)2 C(CH2)s) and t-octyl (-C(CH?)2CH2 C(CH2)s). Preferred R's are methyl and -(CH2)4 -. When using a non-ionic base as a catalyst, the polymerization can be carried out at temperature of between about 25°C to about 200°C depending on the ty pe of polyamide being polymerized. In general, the lower the monomer molecular weight, the lower the polymerization temperature would be.

[0019] The catalyst may be used in an amount of about 0.5 to about 50% by weight or higher, based on the 2- pyrrolidone monomer, preferably 5 to 30 wt.%, most preferably 8 to 20 wt.%.

[0020] The preferred proportions of CO2 and alkaline polymerization catalyst has been found to be about 2 to about 20 mols of the catalyst per mol of CO2, or alternatively between about 4 to about 10 mols of catalyst per mol of CO2. The temperature at which the CO2 is added to the catalyst may be varied widely, where results can be obtained at temperatures ranging from 18°C (approximately the freezing point of the solution of the catalyst in monomer) to 130°C or higher, or between about 40°C to about 60°C.

[0021] In some aspects, an alkaline polymerization catalyst is the alkali metal salt of 2- pyrrolidone, e g. sodium or potassium pyrrolidonate. When CO2 is bubbled through a reactionmixture of 2-pyrrolidone monomer and the alkali metal pyrrolidonate catalyst, an adduct of CO2 and alkali metal pyrrolidonate is formed. It has been found that this adduct can be used in the polymerization when alkali metal pyrrolidonate is also present.

[0022] The CO2 can be bubbled through a mixture of the 2-pyrrolidone monomer and alkali metal pyrrolidonate in the ratio of about one-quarter to about one mol of CO2 per mol of alkali metal pyrrolidonate, although more or less CO2 can be used. If larger amounts of CO2 are used, e.g. more than one-half mol of CO2 per mol of alkali metal pyrrolidonate, the additional CO2 may not be readily absorbed. If smaller amounts of CO2 are used, e.g. 2 mols of alkali metal pyrrolidonate per 0.5 mol of CO2 the reaction mixture will comprise 2-pyrrolidone monomer, alkali metal pyrrolidonate and the CO2 -alkali metal pyrrolidonate adduct. Good results are obtained in general, by stopping the addition of the CO2 just short of absolute saturation, although this is not essential. Best results are obtained by using somewhat less than 1 / 2 mol of CO2 per mol of alkali metal pyrrolidonate, such as a ratio of 1 / 4 to 3 / 8 mol of CO2 per mol of the pyrrolidonate. In any case, the reaction mixture is then placed in a polymerization vessel to polymerize the monomer with or without further addition of CO2. If desired the reaction between CO2 and alkali metal pyrrolidonate can be carried out before contact with the bulk of the 2- pyrrolidone monomer.

[0023] While described herein as occurring in the presence of CO2, the process can also occur without the addition of any CO2, where the remaining components and conditions can remain the same. In the even that no CO2 is added in the process, the polymerization will occur as described, but occurs over much longer timescales and to lower conversation rates.

[0024] In some aspects, the polymerization of 2-pyrrolidone can be carried out in the following manner. First, the 2-pyrrolidone monomer is reacted with an alkali metal hydroxide, preferably NaOH or KOH, the water formed in the reaction being removed by distillation, so as to form in situ an anhydrous solution of the alkali metal salt of the 2-pyrrolidone in the 2-pyrrohdone to be polymerized. Removal of the water can occur under sub-atmospheric conditions (e.g., at pressures below atmospheric pressure of 14.7 psia) and temperatures from 18°C to 150°C, preferably between 25°C to 100°C, and most preferably between 25°C and 45°C. In the presence of water deleterious reactions can occur and cause ring-opening of 2-pyrrolidone monomer and inhibit the polymerization reaction. Instead of the alkali metal hydroxide, the alkali metal pyrrolidonate can be formed using an alkali metal alcoholate, preferably NaOCHs or KOCH3 to form a solution of alkali metal pyrrolidonate in 2-pyrrolidone. Any source of alkali metal can be used to form the pyrrolidonate. provided that undesired by-products are not formed and that the sensitive pyrrolidone ring is not destroyed. Undesired by-products are those that act aspolymerization inhibitors. Sodium metal is an example of a source of alkali metal that should not be used. After removal of water from the reaction mixture, CO2 can be bubbled through to form the alkali metal pyrrolidnale-CCh adduct in situ, thereby starting the polymerization. If desired, additional 2-pyrrolidone monomer can be added to the alkali metal pyrrolidonate solution before introduction of the CO2 Suitably, the 2-pyrrolidone monomer can be contacted with 0.01 to 10 wt.% of CO2 based on the weight of the 2-pyrrolidone monomer. For example, amounts 0.2 to 6 wt.%. based on the weight of the 2-pyrrolidone, or alternatively 0.5 to 3 wt.% can be used.

[0025] Alternatively, polymerization of 2-pyrrolidione can occur by reaction of monomer with potassium tertbutoxide. This base, or similar bases, can be used in similar methods as those described above, where the conditions and components can otherwise be the same or similar. However, in the example of use of potassium tertbutoxide, removal of tertbutanol occurs, as opposed to water. The removal of the tertbutanol can be carried out at a temperature about 100°C, for example betw een 100°C and 150°C. Apart from that the reaction proceeds as described above.

[0026] The amount of carbon dioxide can also be expressed as a mol percent of the mols of alkaline polymerization catalyst. The amount of carbon dioxide ould thus be from about 0.06 to 60 mol percent, based on the mols of the alkaline polymerization catalyst, but higher amounts, e.g. up to about 80 mol percent CO2 based on the mols of alkaline polymerization catalyst have been used. Generally, the amount of CO2 on a molar basis will be from 10 to 80 mol percent, based on the mols of alkaline polymerization catalyst.

[0027] It is possible to introduce CO2 into the system other than by bubbling CO2 into the mixture of 2-pyrrolidone and alkaline polymerization catalyst. For example, the source of CO2 can be a compound that will transfer CO2 to the mixture of 2-pyrrolidone monomer and alkaline polymerization catalyst, provided that the anion remaining after loss of CO2 from the compound is not deleterious to the polymerization. Adducts of carbon dioxide and an alkali metal or quaternary7ammonium pyrrolidonate can be added to a mixture of 2-pyrrolidone monomer and alkaline polymerization catalyst, as can adducts of CO2 and an alkali metal or quaternary ammonium caprolactamate, with or without any CO2 gas added to the system. These adducts are added to the system on the same weight basis as the CO2. A convenient method for preparing the adducts is to bubble CO2 through an anhydrous mixture of the pyrrolidonate and 2- pyrrolidone under vacuum until there is a sharp rise in pressure indicating that the CO2 is no longer being readily absorbed. The adduct is precipitated by adding benzene or other organic precipitant to the solution. There is recovered from the precipitate a free flowing,nonhygroscopic, white powder. Alternatively, the organic precipitant can be added to an anhydrous solution of pyrrolidonate in 2-pyrrolidone before the CO2 is bubbled through the solution, in which case the precipitate forms as the CO2 is absorbed. Since it is necessary to react CO2 with anhydrous pyrrolidonate, it is preferred to form the CO2 -pyrrolidonate adduct by adding CO2 to an anhydrous solution of pyrrolidonate in 2-pyrrolidone, where the pyrrolidonate is formed in situ as described herein.

[0028] In a similar manner, the adduct of CO2 and caprolactamate is formed by bubbling CO2 through an anhydrous solution of caprolactamate in caprolactam and adding the organic precipitant before or after the CO2 addition. Generally, when the caprolactamate is formed in situ, temperatures in excess of 90°C are avoided.

[0029] In some aspects, carbon dioxide can be used as the sole polymerization activator, although other polymerization activators may be used in conjunction with carbon dioxide. Other activators which may be used in conjunction with carbon dioxide are acyl compounds, e.g., organic acyl peroxides, carboxylic acid anhydrides, lactones, lactides. N-acyl derivatives of lactams, acyl halides, and alcohol esters of carboxylic acids.

[0030] In addition, any of the following activators may be used: Carbon disulfide, N-substituted secondary amides, Cyanuric chloride, Organic isocyanates, Adipimide, N-iminopyrrolidones, N- monocarbonyl pyrrolidone and organic acid amide, Aromatic carbonyl and organic acid amide, Chlorine, bromine, N bromopyrrolidone, or N-chloropyrrolidone, NO2 or organic nitrite, P2O5 and other oxides or Group V elements, N,N-disubstituted ureas, Halides and oxy halides of sulfur and phosphorous. Oxides of Group VI elements, Halosilanes, Benzenephosphorus dichloride, benzene phosphorous oxychloride, phosphorous trichloride, thionyl chloride, and / or tetramethylammonium chloride. These activators can be used as a replacement for CO2, or in addition to CO2 for the polymerization reaction. They can be added before, or preferably after the addition of CO2. For example, in the case of tetramethylammonium chloride, the CO2 adduct is formed then tetramethylammonium chloride is added to the solution, mixed well, and the polymerization occurs.

[0031] In general, the polymerization can be performed in the substantial absence of water, although anhydrous conditions are not essential. For example, the amount of water may be less than about 1% by weight of the 2-pyrrolidone monomer, or alternatively less than about 0.1% by weight of the 2-pyrrolidone monomer. The 2-pyrrolidone used in the polymerization may be substantially pure. For example, the 2-pyrrolidone monomer be purified by fractional distillation under reduced pressure or by recrystallization or a combination of both.

[0032] The resulting polymerized polypyrrolidone can have the formula as shown above as formula 1. Other polyamides can also be used for modification herein, where the more general polyamide formula is shown in Formula 2. For example, nylon 3 can be made using a ringopening polymerization beta-propirolactam using bases as described herein, or acrylamide can be polymerized to produce the polyamide. Similarly, Nylon-2 can be synthesized using the polymerization of glycine N-carboxy anhydride (NCA), as well as any other suitable methods. Other polyamides can be produced using any suitable methods.

[0033] In order to improve the stability of the resulting polypyrrolidone, the structure of the poly pyrrolidone can be modified to some degree to alter the properties of the polymer. In some aspects, the amide groups on the backbone structure of the polypyrrolidone can be modified between about 0. 1% to about 10%. or between about 0.2 % to about 8%, or between about 0.5% and about 5%. As used herein the percentage modification refers to the number average modifications of the amide units or groups on the polypyrrolidone backbone.

[0034] The resulting substituted polypyrrolidone can have the following formula:Formula 3where n is as shown in formula 1, m is the same as in formula 1, and any of Ri, R2, and R3 can comprise a hydrogen or an alky l substituent. Other substituents suitable for substitution as R can include methoxy, methylol, methyl-methoxy, and the like. In some aspects, this can result in R = MeOH, MeOMe, MeOEt, or MeOR. In various aspects, R can be any alkyl group using the appropriate substituent. In some aspects, the oxygen included in the repeating unit, sulfur can be incorporated or used to alter the polymer properties. While various methyl groups have been provided, the groups could also include EtOH, EtOMe, which is within the group defined by a alky l group herein. The term "alkyl" as used herein can refers to both straight-chain and branched-chain alkyl groups and includes alkylene. Typical alkyl groups include for example methyl, methylene (— CH2 -), ethyl, isopropyl, n-butyl, t-butyl, hexyl, decyl, tetradecyl, 4-methyl hexadecyl, eicosyl, and the like. The term alkyd includes low er alkyl groups where "lower alkyd" refers to alkyd groups having from 1 through 6 carbon atoms.

[0035] In some aspects, the R group can be a reactive group. For example, the R group can be an epoxy, isocyanate, or similarly reactive constituent. The ability to modify the backbone withsuch groups can be effected in the same manner as described herein, and the reactive groups can alter the chemistry of the resulting polymer.

[0036] As shown in Formula 2, the modifications can be associated with the amide group in the polypyrrolidone, and the remaining groups, including the carboxyl group may not be significantly modified, and in some aspects, the carboxyl group may have less than a 0.1% modification in the final polypyrrolidone composition.

[0037] The modification process of the polypyrrolidone can be effected by contacting poly-2- pyrrolidone (formula 1) with a base to deprotonate the amide backbone, followed by an alkylating agent under reactive conditions. Alternatively, or additionally, the polymer can be reacted with formaldehyde with or without exposure to alcohols or thiols, to modify the amide backbone. This process is typically conducted at temperatures in the range of about 18°C to about 265°C. for about from 0.1 to about 120 hours. Typically, about from 0.1 to 10 moles of the modification agent are used per mole of the polypyrrolidone. The base polymer can be contacted as a finely divided powder in order to maximize contact of the polymer with the modification solution. Additionally, the base polymer can be dissolved in a suitable solvent for reaction. Such suitable solvents are organic acids such as formic acid, fluorinated alcohols (hexafluoroisopropanol), polar protic (DMF), polar aprotic (DMSO, DMAc, NMP), or any solvent in which both the polymer and reactants are soluble. Reaction rates are generally dependent upon temperature and thus lower reaction times can be used with higher reaction temperatures and vice versa. The degree of substitution can be controlled accordingly by adjusting the reaction times and temperatures as well as the above reaction conditions.

[0038] Suitable modification agents which can be used to modify the polypyrrolidone as described herein can include, but are not limited to, formaldehyde, paraformaldehyde, methyliodide, methanol, ethanol, sodium hydride, etc.

[0039] In some aspects, the polypyrrolidone can also be modified at one or more end caps, for example in addition to the backbone modifications. In these aspects, the polypyrrolidone can be reacted with certain alkanolamines or alkylenepoly amine [e.g., NH2(CH2)nNH2], or in some aspects, acid halides or anhydrides (e.g.. acid chlorides, etc.), for a sufficient period of time to effect the desired capping. The end groups of the poly pyrrolidone can be labile and open under very mild conditions, such as upon contact with water at room temperature.

[0040] The end capping can result in the capping of one or more ends such as any carboxyl end groups. Where direct capping of end groups is used the molecular weight of the product is close to (but. generally slightly less than) the weight average molecular weight of the starting material polymer. The capping process of the present invention can be effected by contactingpolypyrrolidone before or after any backbone modifications with an alkanolamine temperature in the range of about from 20°C to 100°C, preferably about from 25°C to 80°C. for about from 0.5 to 50 hours preferably from about 1 to 30 hours.

[0041] The amount of capping agent can be selected to provide a desired amount of end capping. In some aspects, between one to two moles of capping agent can be used per mole of polymer. A molar ratio of 2: 1 between the capping agent and the poly pyrrolidone would theoretically result in both ends of the polypyrrolidone being capped. However, in some aspects an excess of the capping agent (e.g., greater than a 2: 1 ratio of the capping agent to the polypyrrolidone) can be used to ensure adequate contact with the polymer. Thus, typically about from 2 to 10 grams, preferably about from 2 to 4 grams of capping agent can be used per gram of polymer. Alternatively, suitable inert organic diluents or inert organic solvents for the capping agent can also be advantageously used to reduce the amount of alkanolamine and / or alkylenediamine required to maximize polymer contact and facilitate handling.

[0042] Suitable alkanolamine capping agents which can be used can include, but are not limited to, alkanolamines having from 2 through 12 carbon atoms, preferably from 2 through 6 carbon atoms, and at least one hydroxy substituent and one amino substituent each substituted at different carbon atoms. The alkanolamine can also be optionally substituted with up to, and including a total of five hydroxy and / or amino substituents substituted at different carbon atoms. It is important that the carbon atom contains only a single substituent because compounds having carbon atoms having two amino or two hydroxy or an amino and a hydroxy substituent are unstable and would be expected to degrade either during the initial process and / or in polymer upon melt spinning. Suitable alkanolamines species which can be used include, for example, ethanolamine, 3 -aminopropanol, 10-aminodecanol; 4-amino-2-ethyl-butanol: 2-hydroxy-4- aminobutanol, 2,4-diaminobutanol. 2-hydroxymethyl-5-aminopentanol, and the like.

[0043] Suitable alkylenepolyamines which can be used for the capping process can include, for example, alkylenepoly amines having 2 through 12 carbon atoms preferably 2 through 6 carbon atoms, substituted with 2 through 5 amino substituents each at different carbon atoms and optionally 1 through 3 hydroxy substituents each at different carbon atoms up to and including a total of 5 such substituents. Suitable alkylenepolyamme species include, for example, ethylenediamine, hexamethylenediamine, dodecylene diamine; l,5-diamino-2-methylpentane; 1,2,4-triaminobutane; l,5-diamino-3-hydroxyhexane; l,2,6-triamino-4-3-hydroxyethylhexane, and the like. In terms of capped polymer product thermal stability for a given molecular weight, best results are generally obtained using alkanolamines and especially ethanolamine. Where analkylenepoly amine is used, it is preferred to use an alkylenediamine such as ethylenediamine and hexamethy lenediamine.

[0044] Additionally, various cyclic lactams can be used for the capping process, for example caprolactam, laurolactam, and others.

[0045] The end capping can result in improvements in thermal stability, which can facilitate the melt extrusion and particularly melt spinning of the compositions of the invention at temperatures in the range 260°C to 285°C, or less than about 280°C, or below 275°C.

[0046] The modification of the polypyrrolidone can result in a modified polymer have a lower melting temperature. In some aspects, the melting temperature can be lowered relative to the base polypyrrolidone in an amount of between about 0. 1 to about 20°C, or between about 1 to about 10°C.

[0047] The resulting modified polyprrolidone can have a melting temperature of between about 220°C and about 400°C, or between about 245 °C and about 260°C. In some aspects, the modified polyprrolidone (e.g., based on backbone or end cap modifications) can have a degradation temperature at least about 200°C or at least about 300°C, or alternatively between about 290°C and about 330°C.

[0048] A temperature differential between the melting temperature and the degradation temperature can be expanded to allow for a greater range of temperatures to form useful articles. In some aspects, the temperature can differential can be between about 10°C and about 60°C, which may be greater than the difference between the melting and degradation temperatures of the unmodified polypyrrolidone.

[0049] While described herein with respect to Nylon 4, any suitable polyamide composition can be modified as provided herein. Specifically, the same backbone and end capping processes can be used with other nylons such as Nylon 2. Nylon 3, Nylon 6, and the like. In some aspects, the modifications provided herein can be used with proteins. In some aspects, proteins can be seen as functionalized Nylon 2, and these compounds can be both sourced naturally and also made using new biotech techniques. The resulting chemistry of the proteins can follow that of the polypyrrolidone described herein. In general, the degradation temperature of Nylon 2. Nylon 3, and proteins may be below the melting point of these polymers. The use of the modification techniques as provided herein may allow the melting point to be lowered and / or the degradation temperature to be raised sufficiently to allow the polymers and proteins to be more easily processed using any of the processes described herein.

[0050] The resulting polyamide compositions described herein can be used form various compounds and materials, where One or more additives can be included in the polyamidesdescribed herein. In some aspects, the additives can be added prior to the polymerization reaction and / or blended with the resulting polymer prior to or during extrusion or processing. The additives can comprise any compounds used to improve the performance or properties of the polymers. This can allow a resulting polyamides to be produced having a desired set of properties. In some aspects, the additives can comprise one or more of plasticizer, antioxidant, nucleating agent, clarifying agent, caking agent, anti-caking agent (e.g., slip agents), pigment, flame retardants, dulling agents, reactive extrusion agents, heat stabilizers, lubricants, anti-statics, curing agents, blowing agents, biocides, fillers, reinforcements, chain extenders, or any combination thereof.

[0051] Plasticizers can be added to improve the flexibility, durability and stretchability of the polyamides while reducing melt flow. Plasticizers can reduce shear during the mixing steps of polyamide production and improve impact resistance in the final material. In some aspects, the plasticizers can include, but are not limited to, phthalic esters (PAEs), short, medium, and long chain chlorinated paraffins, (SCCP / MCCP / LCCP); Diisoheptylphthalate (DIHP); DHNUP; Benzyl butyl phthalate (BBP); Bis (2-ethylhexyl)phthalate (DEHP): Bis(2-methoxyethyl) phthalate (DMEP): Dibutyl phthalate (DBP); dipentyl phthalate (DPP). di-(2-ethylhexyl) adipate (DEHA), di-octyladipate (DOA), diethyl phthalates (DEP), diisobutylphthalate (DiBP); Tris(2 chloroethyl)phosphate (TCEP); dicyclohexyl phthalate (DCHP), butyl benzyd phthalate (BBP), diheptyl adipate (DHA). heptyl adipate (HAD), heptyl octyl adipate (HOA), a lactam (e.g., laurolactam, etc.), sulfonamides, modified sulfonamide (e.g.. ortho and para-n-ethyl toluenesulfonamide), and combinations thereof. In some aspects, plasticizers for use with the polyamides can comprise low molecular weight polyamides, for medium and high molecular weight polyamides. Typically, a low molecular weight polyamide plasticizer can have a weight average molecular weight of between about 1,000-20,000 Daltons. The plasticizer can comprise between about 0.5% to about 20% by weight of the overall composition of the polyamide.

[0052] In some embodiments, the plasticizer can comprise a caprolactam, benzene sulfonamide, N-butyl benzene sulfonamide, poly etheramines (commercially available as Elastamine® from Huntsman International LLC), polyvinyl acetates (commercially available as Vinnex® from Wacker Chemie AG), polyvinyl esters, or combinations thereof. In some aspects, the plasticizer can be added in an amount between about 1 to about 20 parts per hundred by weight of the overall composition of the polyamide.

[0053] The plasticizer can result in a reduction in viscosity of the polyamide. In some embodiments, the viscosity’ of the plasticized high molecular weight nylon composition is the “complex” viscosity and it can be determined at, e.g., 230° C using a parallel plate viscometer at1 radian per second; a standard test method is described in ASTM D 4440 and ISO 6721. The plasticizer can be used to reduce the viscosity’ of the pure polyamide between about 5% to about 75%;

[0054] In some embodiment, the polyamide can comprise an antioxidant. Antioxidants can be used in various polymer compositions to delay the overall oxidative degradation of plastics, for example when exposed to ultraviolet (UV) light. The free radicals generated by various conditions such as heat, radiation, and mechanical shear can cause the polyamide to degrade. Suitable antioxidants can include arylamines, phenolics, organophosphites (used to reduce hydroperoxides formed during oxidation to alcohols), butyl ated hydroxy toluene (BHT), 2- and3-t-butyl-4-hydro\y anisole (BHA), bisphenol A (BP A), tris(4-nonyl-phenyl) phosphate (TNPP), and combinations thereof. Other suitable antioxidants useful with the polyamides as disclosed herein can include hindered phenolic antioxidant (e.g., N,N'-l,6-sub-hexyl-II-[3,5-di-tert-butyl-4-hydroxyphenyl propionamide], etc.), a phosphite esters antioxidant (e.g., tri (2,4-ditertrabutyl phenyl) phosphite ester, etc.), or a combination thereof. A suitable antioxidant can include Irganox 1098, which is commercially available from BASF. The antioxidant may be present in an amount of between about 0.05 - 3 wt.%.

[0055] In some embodiments, the polyamide can comprise a nucleating agent and / or a clarifying agent. Nucleating agents serve to initiate the formation of polymer crystals, and clarifying agents are a type of nucleating agent that helps to control or reduce the crystal size to produce a transparent or semi-transparent polymer. Suitable nucleating agents and / or clarifying agents can comprise calcium carboxylates with a long carbon chain as a main component, sorbitol, benzoates, and combinations thereof. The nucleating agents or clarifying agents can comprise between about 0. 1% to about 0.5% by weight of the overall composition of the polyamide.

[0056] In some embodiments, the polyamide can comprise a slip agent. Slip compounds can be used to reduce the surface coefficient of friction of a polymer. In addition to providing lubrication to the polymer surface, they are also used to enhance the polymer with antistatic properties, enable better mold release, reduced melt viscosity, and anti-sticking properties. Suitable slip compounds can include, but are not limited to, fatty acid amides, fatty acid esters, metallic stearates (for example, zinc stearate), waxes, and combinations thereof. The slip agents can comprise between about 0.1% to about 2% by weight of the overall composition of the polyamide.

[0057] In some embodiments, the polyamide can comprise a pigment. The pigment can serve to impart color to the polyamide and / or absorb various light components to increase the stability of the polyamide over time. Examples of colorants can comprise cyan, magenta, yellow, and thelike. Examples of colorants include dyes, such as acid yellow 23(AY 23), acid yellow 17(AY 17), acid red 52(AR 52), acid red 289(AR 289), reactive red 180(RR 180), direct blue 199(DB 199), or pigments, such as pigment blue 15:3(PB 15:3), pigment red 122(PR 122), pigment yellow 155(PY 155), and pigment yellow 74(PY 74). Organic and inorganic pigments can also be used such as cobalt(II) diacetate, cadmium compounds, chromium compounds, lead compounds, zinc sulfide, zinc oxide, iron oxide, cadmium-manganese based, chromium based, ultramarine and titanium dioxide, lead carbonate, bismuth oxychloride, substances with fluorescence, and combinations thereof. The pigments can comprise between about 0.01% to about 10% by weight of the overall composition of the polyamide.

[0058] In some embodiments, the polyamide can comprise a flame retardant. Flame retardants serve to reduce the flammability of the polymer, which can be useful in certain end uses of the polymers. Flame retardant can comprise organic non-reactive compounds, inorganic non- reactive compound, and reactive compounds that reduce the availability of free radicals for combustion. Specific compounds can include, but are not limited to, short, medium, long chain chlorinated paraffins (SCCP / MCCP / LCCP): boric acid; Brominated flame retardants with antimony (Sb) as synergist (e.g. Polybrominated diphenyl ethers (PBDEs); Decabromodiphenylethane; tetrabromobisphenol A (TBBPA)); Phosphorous flame retardant (e.g. Tris(2-chloroethyl)phosphate (TCEP) Tris(2-chlorisopropyl)phosphate (TCPP)); hexabromocyclohexane (HBCDD); phosphate esters, halogenated phosphate esters, halogenated hydrocarbons, antimony oxide, aluminum oxide trihydrate, zinc borate, ammonium orthophosphate, ammonium sulfamate, bromine and / or phosphorus containing polyols, halogenated phenols, tetrachlorophthalic anhydride, phosphonate esters, dibromoneopentyl alcohol, or combinations thereof. The flame retardant(s) can comprise between about 3% to about 25% by weight of the overall composition of the polyamide for reactive flame retardants, or between about 0.5% to about 4 wt.% by weight of the overall composition of the polyamide.

[0059] In some embodiments, the polyamide can comprise a dulling agent. A dulling agents serves to produce a desired level of surface finish in the final polyamide composition or product. Typical dulling agents can comprise titanium oxide, where the amount of the dulling agent can produce the desired surface finish or appearance. The dulling agent can comprise between about 0.1% to about 5% by weight of the overall composition of the polyamide.

[0060] In some embodiments, the polyamide can comprise a reactive extrusion agent. The reactive extrusion agent can serve to cany' out a portion of the polymerization reaction during the extrusion process. When mixed with the polymer, the reactive extrusion agent can serve to further react components of the polymer as the polymer is heated for extrusion. The reactiveextrusion agent can comprise any of the initiators as described herein including a peroxide. When the polymer is heated for extrusion, a reaction (e.g. a grafting reaction, etc.) may occur in a molten state inside of an extruder.

[0061] In some embodiments, the polyamide can comprise a heat stabilizer. Heat stabilizers can be used to help prevent or reduce the thermal degradation of polymers when exposed to elevated temperatures such as during processing of the polymer or during use of the polymer. Suitable heat stabilizers can include, but are not limited to. mixed metal salt blends, organotin compounds, lead compounds, alkylorganophosphites, epoxy compounds, and beta diketones. In general, epoxy stabilizers can be derivatives of epoxidized soybean oil (ESBO), linseed oil, and sunflower oil, most commonly found in food packaging plashes. Other suitable heat stabilizers can comprise cuprous iodide, potassium iodide, phenolic antioxidant(s). aromatic amine(s). copper or mantoquita, KI or KBr, and combinations thereof. The heat stabilizers may be present in an amount of between about 0.05 - 3 wt.% by weight of the overall composition of the polyamide.

[0062] In some embodiments, the polyamide can comprise a lubricant. The lubricant can sen e to reduce the surface friction of the polymer with the processing equipment. In some aspects, the lubneant can comprise ultra-high molecular weight polyethylene, PTFE (polytetrafluoroethylene), and any combination thereof. The heat stabilizers may be present in an amount of between about 0.1 - 0.3 wt.% by weight of the overall composition of the polyamide.

[0063] In some embodiments, the polyamide can comprise an anti-static compound. An antistatic compound refers to a component that can reduce or eliminate static electricity. Suitable anti-static components can include, but are not limited to, metal fibers, powders, or flakes (steel, copper or other metal), metal-plated polymeric material, and polymeric materials incorporating a conductive carbon such as carbon black, graphite, graphene on the surface and / or in the interior of the material, and the like. As an example, a nylon fiber, powder, or flake can be coated with a metal (e.g. , silver) layer to serve as an anti-static compound. The heat stabilizers may be present in an amount of between about 0.2 - 5 wt.% by weight of the overall composition of the polyamide.

[0064] In some embodiments, the polyamide can comprise a curing agent. Curing agents can be introduced as part of the polymerization process or after the polymerization process to further react any unreacted monomers and / or further polymerize the polyamide. The curing agents can generally comprise any peroxides or other crosslinkers, catalysts, or accelerators used in the polyamide process. Suitable examples of curing agents can include, but are not limited to. 4,4?- Diaminodiphenylmethane (MDA); 2,2’-dichloro-4,4’-methylenedianiline (MOCA);Formaldehyde - reaction products with aniline; hydrazine; l,3,5-Tris(oxiran-2-ylmethyl)-l,3,5- triazinane-2, 4, 6-trione (TGIC) / l,3,5-tris[(2S and 2R)-2,3-epoxypropyl]-l,3,5- triazine-2,4,6- (1H,3H,5H)- tri one (|3-TGIC), or combinations thereof. The curing agents may be present in an amount of between about 0.1 - 3 wt.% by weight of the overall composition of the polyamide.

[0065] In some embodiments, the polyamide can comprise a blowing agent. Blowing agents serve to form a gas during the polymer production process to generate a foam. The blowing agents can be mixed into or injected into the monomer reactants during polymerization. Examples of physical blowing agents include hydrocarbons, halogenated hydrocarbons, carbon dioxide, azodicarbonamide, benzene disulphonyl hydrazide (BSH), pentane, CO2, or combinations thereof. Typically, the physical blowing agent can be introduced in-line (e.g., directly, into the mixing head), or in batch operation via a storage tank. The blowing agent may not remain in the final product, and the amount used can be determined by the density of the foam desired.

[0066] In some embodiments, the polyamide can comprise a biocide. A biocide can serve to prevent the grow th or formation of bacteria, mold, or other biological growths on the final product, which can in some aspects be a foam. The biocide may be, for example, an aldehyde- releasing biocide, an aldehyde-based biocide, a phenolic biocide, an isothiazolin biocide or any mixture thereof. The biocide can be selected from one or more of formaldehyde, methanol, sodium hypochlorite, acetaldehyde, glyoxal, succinaldehyde, glutaaldehyde. 2-propenal, dialdehyde phthalate and mixtures thereof. Also, in certain embodiments, formaldehyde, glutaaldehyde, benzy l alcohol mono (poly) -hemiformal, ethylene glycol hemiformal (EGHF), [1,2-ethanediylbis (oxy)]-bis-methanol, tetrahydro- 1,3, 4,6-Tetrakiss (hydroxylmethyl) imidazole [4,5-d] imidazole-2,5 (1H, 3H) -dione (generally referred to as tetramethylol acetylene diurea, TMAD), orthophenylphenol (OPP) ). 2-Methyl-4-isothiazolin-3-one (MIT), 5-chloro-2- methyl-2H-isothiazolin-3-one (CIT), l,2-benzoisothiazolin-3-one (BIT), Or a mixture thereof. The biocide may be a combination of 2-methyl-4-isothiazolin-3-one (MIT) and 1,2- benzoisothiazolin-3-one (BIT). The biocide may be, for example, aminoalcohols such as ethanolamine and dimethylethanolamine, arsenic compounds, organic tin compounds, triclosanor, or combinations thereof. The amount of biocide present in the composition is, for example, 1 ppm to about 2000 ppm by weight of the overall composition of the polyamide.

[0067] In some embodiments, the polyamide can comprise a filler or reinforcing agent. Suitable rigid fillers that are can be used include fibrous (like glass fibers), spherical (like glass beads) or flake-shaped (like mica) materials. Reinforcing agents can compnse fibrous fillers such aschopped glass fibers, which can be randomly, partially, or substantially fully orientated to produce various levels of modulus and strength properties. Any suitable materials such as glass, carbon, aramide, calcium carbonate, talk, clay, zinc oxide, glimmer, metal powder, wood powder, asbest, barium sulphate, glass microspheres, silicious earth, or any combination thereof. The fillers may be present in an amount up to about 50 wt.% by weight of the overall composition of the polyamide, and reinforcing agents can be present in an amount of between about 10 wt.% to about 30 wt.% by weight of the overall composition of the polyamide.

[0068] In some embodiments, the polyamide can comprise a chain extender. The use of chain extenders can modify the rheological properties of the polyamide, including the viscosity. Any suitable chain extenders can be used such as epoxy-type chain extenders, amine-based chain extenders (e.g., primary, secondary, and / or tertiary amines sch as alkanolamines including ethanolamine). The chain extenders can undergo reactive modification of the polyamides during the modification process.EXAMPLES

[0069] The disclosure having been generally described, the following examples are given as particular embodiments of the disclosure and to demonstrate the practice and advantages thereof. It is understood that the examples are given by way of illustration and are not intended to limit the specification or the claims in any manner.EXAMPLE 1

[0070] Example 1 : In this example, 0.5 g of polypyrrolidone was dissolved in 17 mL of formic acid at 60°C. 57 mg of paraformaldehyde was suspended in 680 mg of methanol at 60°C. An additional 680 mg of methanol was also incubated at 60°C. Upon complete dissolution of the polypyrrolidone into formic acid the paraformaldehyde solution was added in a rapid manner. The formic acid solution now containing polypyrrolidone, paraformaldehyde, and methanol was allowed to react at 60°C for 5 minutes. At the end of this time the additional 680 mg of methanol was rapidly added to the solution and reacted for 30 minutes. Following the reaction time, the solution was added dropwise into 350 mL of cold acetone. The precipitate was then removed and soaked in 150 mL of clean acetone for 10 minutes, removed and dried at 50°C. The melting point of this sample was 259° C with a degradation temperature of 313°C. The starting polypyrrolidone melting point temperature and degradation temperature was 267°C and 288°C, respectively.EXAMPLE 2

[0071] Example 2: Similar reaction conditions as Example 1 were used except that 100 mg of paraformaldehyde was suspended in 680 mg of methanol. Additionally, the reaction time after addition of the paraformaldehyde suspension was 10 minutes. This sample displayed a melting point temperature of 226°C and a degradation temperature >304°C.EXAMPLE 3

[0072] Example 3: The reactions conditions were similar as above except that 159 mg of paraformaldehyde was suspended in 680 mg of methanol. This sample displayed a melting point temperature of 218°C and a degradation temperature of >303°C.EXAMPLE 4

[0073] Example 4: 1.07 g of polypyrrolidone was added to a vial containing 1.6 g of formic acid, 1.07 g of paraformaldehyde, and 5.4 mL of methanol. The vial was shaken by hand, sealed, and placed into an oven at 50°C for 119 hours. The sample was then washed with excess 1 :1 acetone: water, filtered, then w ashed with excess acetone. The sample was dried. This sample displayed a melting point temperature of 263°C, and a degradation temperature of 306°C.EXAMPLE 5

[0074] Example 5: Polymerization of pyrrolidione into polypyrrolidone occurred by mixing 11.2 g of pyrrolidone with 0.869 g of KOH at 110°C, under N2, until complete dissolution of the KOH. The sample was then further stirred at least 10 minutes following complete dissolution. Dehydration occurred via short-path distillation; approximately 10% by volume was removed to ensure dryness. The reaction was then cooled to <60°C under an N2 atmosphere, following which CO2 was bubbled through the solution to produce a cloudy yellow suspension. This was then placed in a scintillation vial and in an oven at 50°C for at least 8 hours. Following the reaction, the solid polypyrrolidone was removed from the vial, mechanically crushed into small pieces, washed with excess water, and dried. The melting point temperature was 263°C.EXAMPLE 6

[0075] Example 6: Similar polymerization conditions as Example 5, except after addition of CO2 to the solution 1.422 g of tetramethylammonium chloride (pre-dried) was added and stirred for 5 minutes. This complete solution was then transferred to a vial, placed in an oven at 50°C and reacted for at least 8 hours. Purification proceeded as Example 5. The melting point temperature of this sample was 264°C, with a degradation temperature of 282°C.EXAMPLE 7

[0076] Example 7: The purified sample from Example 6 was dissolved in formic acid and precipitated in water. The sample was then filtered and washed with excess water to neutralizethe solution. The polypyrrolidone was then dried. This sample has a melting point temperature of 266°C. with a degradation temperature of 299°C.EXAMPLE 8

[0077] Example 8: Polymerization of pyrrolidone occurred as with Example 5 and 6, except in place of KOH, 1.477 g of potassium tert-butoxide was used. Following purification this sample had a melting point temperature of 267°C, with a degradation temperature of 285 °C.EXAMPLE 9

[0078] Example 9: Polymer from Example 8 was dissolved in formic acid and purified as in Example 7. This sample had a melting point of 264°C, with a degradation temperature of 294°C.EXAMPLE 10

[0079] Example 10: 1 g of polypyrrolidone was mixed with 3 g of ethanolamine. This vial was kept at 150°C for 40 minutes. The vial was then cooled, and the polymer was washed with excess water and dried. This sample as a melting point temperature of 268°C, with a degradation temperature of 304 °C.EXAMPLE 11

[0080] Example 11 : A sample of polypyrrolidone which has undergone melting point depression (Example 2) w as then reacted with ethanolamine to alter the end capping (as in Example 10). This sample then show ed a melting point temperature of 231 °C, with a degradation point > 321°C.

[0081] Having described certain compositions and methods, specific aspects can include, but are not limited to:

[0082] In a first aspects, a polyamide comprises a plurality of amide units forming a polymer chain; and an alky l substituent on the amide group, wherein the polyamide has a substitution of the amide units in an amount of between about 0.1% to about 10% of the amide units in the polymer chain.

[0083] A second aspect can include the polyamide of the first aspect, wherein the polymer chain comprises end caps, and wherein at least a portion of the end caps comprise an alkyd substituent.

[0084] A third aspect can include the polyamide of the first or second aspect, wherein alkyd substituent is a methyl, ethyl, or butyl group.

[0085] A fourth aspect can include the polyamide of any one of the first to third aspects, wherein the polymer is biodegradable.

[0086] A fifth aspect can include the polyamide of any one of the first to fourth aspects, wherein the polymer is in the form of a sheet, a film, a filament, a ribbon, a molded article, a woven material, or a fiber.

[0087] A sixth aspect can include the polyamide of any one of the first to fifth aspects, wherein the polymer has a melting point of between 220°C and about 400°C.

[0088] A seventh aspect can include the polyamide of any one of the first to sixth aspects, wherein the polymer has a degradation temperature of at least about 200°C.

[0089] An eighth aspect can include the polyamide of any one of the first to seventh aspects, wherein the polymer has a temperature difference between a melting temperature and a degradation temperature of at least about 20°C.

[0090] A ninth aspect can include the polyamide of any one of the first to fifth aspects, wherein the polyamide is Nylon 2, Nylon 3, Nylon 4, Nylon 6, or a protein.

[0091] In a tenth aspect, a poly-2-pyrrolidone polymer comprises a formula as follows:where m is 3 and where R comprises an alkyl substituent on the amide group, and where the poly -2-pyrroli done has a substitution of the amide group in an amount of between about 0.1 % to about 10% of the amide groups in the poly-2-pyrrolidone.

[0092] An eleventh aspect can include the polymer of the tenth aspect, wherein R is a methyl, ethyl, or butyl group.

[0093] A twelfth aspect can include the polymer of the eleventh aspect, wherein the polymer has a melting point of between 220°C and about 400°C.

[0094] A thirteenth aspect can include the polymer of any one of the tenth to twelfth aspects, wherein the polymer has a degradation temperature of at least about 200°C.

[0095] A fourteenth aspect can include the polymer of any one of the tenth to thirteenth aspects, wherein the polymer has a temperature difference between a melting temperature and a degradation temperature of at least about 20°C.

[0096] A fifteenth aspect can include the polymer of any one of the tenth to fourteenth aspects, wherein the polymer is biodegradable.

[0097] A sixteenth aspect can include the polymer of any one of the tenth to fifteenth aspects, wherein the polymer is in the form of a sheet, a film, a filament, a ribbon, a molded article, a woven material, or a fiber.

[0098] In a seventeenth aspect, a method of forming a polyamide composition comprises: providing a polyamide, wherein the polyamide comprises a plurality of amide groups in abackbone structure of the polyamide; and modify ing a portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents to form the polyamide composition, wherein the polyamide has a substitution of the amide units in an amount of between about 0. 1% to about 10% of the amide units in the backbone.

[0099] An eighteenth aspect can include the method of the seventeenth aspect, wherein the polyamide composition has a formal of:where R comprises an alkyl substituent on an amide group of the plurality of amide groups.A nineteenth aspect can include the method of the seventeenth aspect, wherein the polyamide composition has the following formula:where n is between 200 and 100,000. m is 1-11, and any of Ri, R2, and R3 can compnse a hydrogen or an alkyl substituent.

[0100] A twentieth aspect can include the method of any one of the seventeenth to nineteenth aspects, where the carboxyl group in the polyamide has less than a 0. 1% modification in the polyamide composition.

[0101] A twenty first aspect can include the method of any one of the seventeenth to twentieth aspects, wherein modifying the portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents comprises: contacting the polyamide with a modification agent; deprotonating the portion of the plurality of amide groups; and alkylating the portion of the plurality of amide groups to form the polyamide composition.

[0102] A twenty second aspect can include the method of the twenty first aspect, wherein modifying the portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents further comprises: dissolving the polyamide in a solvent prior to contacting the polyamide with the modification agent.

[0103] A twenty third aspect can include the method of the twenty first or twenty second aspect, wherein the modification agent comprises a base, formaldehyde, paraformaldehyde, methyliodide, methanol, ethanol, sodium hydride, or any combination thereof.

[0104] A twenty fourth aspect can include the method of any one of the seventeenth to twenty fifth aspects, wherein modifying the portion of the plurality of amide groups occurs at a temperature in a range of 18°C to about 265°C, and for a time between about 0.1 to about 120 hours.

[0105] A twenty fifth aspect can include the method of any one of the seventeenth to twenty fourth aspects, further comprising: modifying a portion of the end caps of the polyamide composition.

[0106] A twenty sixth aspect can include the method of the twenty fifth aspect, wherein modifying the portion of the end caps comprises using capping agents to modify the end caps, wherein the capping agents comprise alkanolamines, alkylenepolyamine, cyclic lactams, or any combination thereof.

[0107] In a twenty seventh aspect, a polyamide comprises: a plurality of amide units forming a polymer chain; and an alkyl substituent on the amide group, wherein the polyamide has a substitution of the amide units in an amount of between about 0. 1 % to about 10% of the amide units in the polymer chain, and wherein the polyamide comprises one or more additives.

[0108] A twenty eighth aspect can include the polyamide of the twenty seventh aspect, wherein the polymer chain comprises end caps, and wherein at least a portion of the end caps comprise an alkyl substituent, wherein alkyl substituent is a methyl, ethyl, or butyl group.

[0109] A twenty ninth aspect can include the polyamide of the twenty seventh aspect, wherein the polyamide is Nylon 2. Nylon 3, Nylon 4, Nylon 6, or a protein.

[0110] A thirtieth aspect can include the polyamide of any one of the twenty seventh to twenty ninth aspects, wherein the one or more additives comprise a plasticizer, an antioxidant, a nucleating agent, a clarifying agent, a caking agent, an anti-caking agent, a pigment, a flame retardant, a dulling agent, a reactive extrusion agent, a heat stabilizer, lubricants, an anti-static component, a curing agent, a blowing agent, a biocide, a filler, a reinforcement additive, or any combination thereof.

[0111] A thirty first aspect can include the polyamide of any one of the twenty' seventh to thirtieth aspects, wherein the one or more additives comprise a plasticizer, and wherein the plasticizer comprises a lactam (e.g. caprolactam), benzene sulfonamide, N-butyl benzene sulfonamide, modified sulfonamides (e.g. ortho and para-n-ethyl toluenesulfonamide), polyetheramines, polyvinyl acetates, polyvinyl esters, or combinations thereof.

[0112] A thirty second aspect can include the polyamide of any one of the twenty seventh to thirty first aspects, wherein the one or more additives comprise a nucleating or clarifying agent, and wherein the nucleating or clarifying agent comprises a calcium carboxylate with a long carbon chain as a main component, sorbitol, benzoates, or combinations thereof.

[0113] A thirty third aspect can include the polyamide of any one of the twenty seventh to thirty second aspects, wherein the one or more additives comprise a slip agent, wherein the slip agent comprises a fatty acid amide, a fatty acid ester, a metallic stearate, a wax, or combinations thereof.

[0114] A thirty' fourth aspect can include the polyamide of any one of the twenty seventh to thirty' third aspects, wherein the one or more additives comprise a pigment.

[0115] A thirty fifth aspect can include the polyamide of any one of the twenty seventh to thirty fourth aspects, wherein the one or more additives comprise a flame retardant, and wherein the flame retardant comprises short, medium, long chain chlorinated paraffins (SCCP / MCCP / LCCP), boric acid, a brominated flame retardant, a phosphorous flame retardant, a phosphate ester, a halogenated phosphate ester, a halogenated hydrocarbon, antimony oxide, aluminum oxide trihydrate, zinc borate, an ammonium orthophosphate, ammonium sulfamate, bromine and / or phosphorus containing polyol, a halogenated phenol, tetrachlorophthalic anhydride, a phosphonate ester, dibromoneopentyl alcohol, or any combinations thereof.

[0116] A thirty sixth aspect can include the polyamide of any one of the twenty seventh to thirty fifth aspects, wherein the one or more additives comprise a dulling agent.

[0117] A thirty' seventh aspect can include the polyamide of any one of the twenty seventh to thirty' sixth aspects, wherein the one or more additives comprise a reactive extrusion agent.

[0118] A thirty eighth aspect can include the polyamide of any one of the twenty seventh to thirty seventh aspects, wherein the one or more additives comprise a heat stabilizer, and wherein the heat stabilizer comprises a mixed metal salt, an organotin compound, a lead compound, an alkylorganophosphites, epoxy compound, a beta diketone, cuprous iodide, potassium iodide, a phenolic antioxidant, an aromatic amine, copper or mantoquita, KI, KBr, or any combinations thereof.

[0119] A thirty7ninth aspect can include the polyamide of any one of the twenty' seventh to thirty' eighth aspects, w herein the one or more additives comprise a lubricant.

[0120] A fortieth aspect can include the polyamide of any one of the twenty seventh to thirty ninth aspects, wherein the one or more additives comprise an antistatic compound,wherein the antistatic compound comprises a metallic fiber, a metallic powders, a metallic flakes, a metal-plated polymeric material, a conductive carbon, or any combination thereof.

[0121] A forty first aspect can include the polyamide of any one of the twenty seventh to fortieth aspects, wherein the one or more additives comprise a curing agent, wherein the curing agent comprises 4,4’- diaminodiphenylmethane (MDA); 2,2'-dichloro-4,4’- methylenedianiline (MOCA); Formaldehyde - reaction products with aniline; hydrazine; 1,3,5- Tris(oxiran-2-ylmethyl)-1.3.5-triazinane-2, 4, 6-trione (TGIC) / 1.3.5-tris[(2S and 2R)-2,3- epoxypropyl]-l,3,5- triazine-2,4,6-(lH,3H,5H)- trione (P-TGIC), or any combinations thereof.

[0122] A forty second aspect can include the polyamide of any one of the twenty seventh to forty first aspects, wherein the one or more additives comprise a blowing agent.

[0123] A forty third aspect can include the polyamide of any one of the twenty seventh to forty second aspects, wherein the one or more additives comprise a biocide, wherein the biocide comprises formaldehyde, methanol, sodium hypochlorite, acetaldehyde, glyoxal, succinaldehyde, glutaaldehyde, 2-propenal, dialdehyde phthalate, glutaaldehyde, benzy l alcohol mono (poly) -hemiformal, ethylene glycol hemiformal (EGHF). [1,2-ethanediylbis (oxy)] -bis-methanol, tetrahydro- 1,3, 4,6-Tetrakiss (hydroxylmethyl) imidazole [4,5-d] imidazole-2,5 (1H, 3H)-dione, orthophenylphenol (OPP) ), 2-Methyl-4-isothiazolin-3-one (MIT), 5-chloro-2-methyl-2H-isothiazolin-3-one (CIT), l,2-benzoisothiazolin-3-one (BIT), Or a mixture thereof. The biocide may be a combination of 2-methyl-4-isothiazolin-3-one (MIT), l,2-benzoisothiazolin-3-one (BIT), or any combination thereof.

[0124] A forty fourth aspect can include the polyamide of any one of the twenty seventh to forty third aspects, wherein the one or more additives comprise a filler or reinforcing agent, and wherein the filler or reinforcing agent comprises glass, carbon, aramide, calcium carbonate, talk, clay, zinc oxide, glimmer, metal powder, wood powder, asbest, barium sulphate, glass microspheres, silicious earth, or any combination thereof.

[0125] In a forty7fifth aspect, a method of forming a polyamide composition, the method comprises: providing a polyamide, wherein the polyamide comprises a plurality7of amide groups in a backbone structure of the polyamide; modifying a portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents to form the polyamide composition, wherein the polyamide has a substitution of the amide units in an amount of between about 0.1% to about 10% of the amide units in the backbone.

[0126] A forty sixth aspect can include the method of the forty fifth aspect, wherein the polyamide composition has a formal of:where R comprises an alkyl substituent on an amide group of the plurality' of amide groups.

[0127] A forty seventh aspect can include the method of the forty fifth or forty sixth aspect, wherein the polyamide composition has the following formula:

[0128] where n is between 200 and 100,000, m is 1-11, and any of Ri, R2, and R3 can comprise a hydrogen or an alky l substituent.

[0129] A forty eighth aspect can include the method of any one of the forty fifth to forty seventh aspects, wherein the one or more additives comprise a plasticizer, an antioxidant, a nucleating agent, a clarifying agent, a caking agent, an anti-caking agent, a pigment, a flame retardant, a dulling agent, a reactive extrusion agent, a heat stabilizer, lubricants, an anti-static component, a curing agent, a blowing agent, a biocide, a filler, a reinforcement additive, or any combination thereof.

[0130] A forty ninth aspect can include the method of any one of the forty fifth to forty eighth aspects, wherein the one or more additives comprise a plasticizer, and wherein the plasticizer comprises a lactam (e.g. caprolactam), benzene sulfonamide, N-butyl benzene sulfonamide, or modifed sulfonamides (e.g. ortho and para-n-ethyl toluenesulfonamide) polyetheramines, polyvinyl acetates, polyvinyl esters, or combinations thereof.

[0131] A fiftieth aspect can include the method of any one of the forty fifth to forty ninth aspects, wherein the one or more additives comprise a nucleating or clarifying agent, and wherein the nucleating or clarifying agent comprises a calcium carboxylate with a long carbon chain as a main component, sorbitol, benzoates, or combinations thereof.

[0132] A fifty first aspect can include the method of any one of the forty' fifth to fiftieth aspectswherein the one or more additives comprise a slip agent, wherein the slip agent comprises a fatty acid amide, a fatty acid ester, a metallic stearate, a wax, or combinations thereof.

[0133] A fifty second aspect can include the method of any one of the forty fifth to fifty first aspects, wherein the one or more additives comprise a pigment.

[0134] A fifty third aspect can include the method of any one of the forty fifth to fifty second aspects, wherein the one or more additives comprise aflame retardant, and wherein the flame retardant comprises short, medium, long chain chlorinated paraffins (SCCP / MCCP / LCCP). boric acid, a brominated flame retardant, a phosphorous flame retardant, a phosphate ester, a halogenated phosphate ester, a halogenated hydrocarbon, antimony oxide, aluminum oxide trihydrate, zinc borate, an ammonium orthophosphate, ammonium sulfamate, bromine and / or phosphorus containing polyol, a halogenated phenol, tetrachlorophthalic anhydride, a phosphonate ester, dibromoneopentyl alcohol, or any combinations thereof.

[0135] A fifty fourth aspect can include the method of any one of the forty fifth to fifty third aspects, wherein the one or more additives comprise a dulling agent.

[0136] A fifty fifth aspect can include the method of any one of the forty fifth to fifty fourth aspects, wherein the one or more additives comprise a reactive extrusion agent.

[0137] A fifty sixth aspect can include the method of any one of the forty fifth to fifty' fifth aspects, wherein the one or more additives comprise a heat stabilizer, and wherein the heat stabilizer comprises a mixed metal salt, an organotin compound, a lead compound, an alkylorganophosphites, epoxy compound, a beta diketone, cuprous iodide, potassium iodide, a phenolic antioxidant, an aromatic amine, copper or mantoquita. KI. KBr. or any combinations thereof.

[0138] A fifty seventh aspect can include the method of any one of the forty fifth to fifty sixth aspects, wherein the one or more additives comprise a lubricant.

[0139] A fifty eighth aspect can include the method of any one of the forty fifth to fifty seventh aspects, wherein the one or more additives comprise an antistatic compound, wherein the antistatic compound comprises a metallic fiber, a metallic powder, a metallic flakes, a metal-plated polymeric material, a conductive carbon, or any combination thereof.

[0140] A fifty ninth aspect can include the method of any one of the forty fifth to fifty eighth aspects, wherein the one or more additives compnse a curing agent, wherein the curing agent comprises 4,4’- diaminodiphenylmethane (MDA); 2,2’-dichloro-4,4’- methylenedianiline (MOCA); Formaldehyde - reaction products with aniline; hydrazine; 1,3,5- Tris(oxiran-2-ylmethyl)-l, 3, 5-triazinane-2, 4, 6-trione (TGIC) / l,3,5-tris[(2S and 2R)-2,3- epoxypropyl]-l,3,5- triazine-2,4.6-(lH,3H,5H)- trione (P-TGIC). or any combinations thereof.

[0141] A sixtieth aspect can include the method of any one of the forty fifth to fifty ninth aspects, wherein the one or more additives comprise a blowing agent.

[0142] A sixty first aspect can include the method of any one of the forty fifth to sixtieth aspects, wherein the one or more additives comprise a biocide, wherein the biocide comprises formaldehyde, methanol, sodium hypochlorite, acetaldehyde, glyoxal, succinaldehyde, glutaaldehyde, 2-propenal. dialdehyde phthalate, glutaaldehyde, benzyl alcohol mono (poly) - hemiformal, ethylene glycol hemiformal (EGHF), [1,2-ethanediylbis (oxy)]-bis-methanol. tetrahydro- 1,3, 4,6-Tetrakiss (hydroxylmethyl) imidazole [4,5-d] imidazole-2,5 (1H, 3H)- dione, orthophenylphenol (OPP) ), 2-Methyl-4-isothiazolin-3-one (MIT), 5-chloro-2-methyl- 2H-isothiazolin-3-one (CIT), l,2-benzoisothiazolin-3-one (BIT), Or a mixture thereof. The biocide may be a combination of 2-methyl-4-isothiazolin-3-one (MIT). 1 ,2-benzoisothiazolin- 3-one (BIT), or any combination thereof.

[0143] A sixty second aspect can include the method of any one of the forty fifth to sixty first aspects, wherein the one or more additives comprise a filler or reinforcing agent, and wherein the filler or reinforcing agent comprises glass, carbon, aramide, calcium carbonate, talk, clay, zinc oxide, glimmer, metal powder, wood powder, asbest, barium sulphate, glass microspheres, silicious earth, or any combination thereof.

[0144] It is to be further understood that the present description is not limited to the particular methodology, compounds, materials, manufacturing techniques, uses, and applications, described herein, as these may vary. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present systems and methods. It must be noted that as used herein and in the appended claims (in this application, or any derived applications thereof), the singular forms "a," "an," and "the" include the plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to "an element" is a reference to one or more elements and includes equivalents thereof know n to those skilled in the art. All conjunctions used are to be understood in the most inclusive sense possible. Thus, the word "or" should be understood as having the definition of a logical "or" rather than that of a logical "exclusive or" unless the context clearly necessitates otherwise. Structures described herein are to be understood also to refer to functional equivalents of such structures. Language that may be construed to express approximation should be so understood unless the context clearly dictates otherwise.

[0145] Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art to which this description belongs. Preferred methods, techniques, devices, and materials are described,although any methods, techniques, devices, or materials similar or equivalent to those described herein may be used in the practice or testing of the present systems and methods. Structures described herein are to be understood also to refer to functional equivalents of such structures. The present systems and methods will now be described in detail with reference to embodiments thereof as illustrated in the accompanying drawings.

[0146] From reading the present disclosure, other variations and modifications will be apparent to persons skilled in the art. Such variations and modifications may involve equivalent and other features which are already known in the art, and which may be used instead of or in addition to features already described herein.

[0147] Although Claims may be formulated in this Application or of any further Application derived therefrom, to particular combinations of features, it should be understood that the scope of the disclosure also includes any novel feature or any novel combination of features disclosed herein either explicitly or implicitly or any generalization thereof, whether or not it relates to the same systems or methods as presently claimed in any Claim and whether or not it mitigates any or all of the same technical problems as do the present systems and methods.

[0148] Features which are descnbed in the context of separate embodiments may also be provided in combination in a single embodiment. Conversely, various features which are, for brevity7, described in the context of a single embodiment, may also be provided separately or in any suitable sub-combination. The Applicants hereby give notice that new claims may be formulated to such features and / or combinations of such features during the prosecution of the present Application or of any' further Application derived therefrom.

Claims

CLAIMSWhat is claimed is:

1. A polyamide comprising: a plurality' of amide units forming a polymer chain; and an alkyl substituent on the amide group, wherein the polyamide has a substitution of the amide units in an amount of between about 0. 1% to about 10% of the amide units in the polymer chain, and wherein the polyamide comprises one or more additives.

2. The polyamide of claim 1, wherein the polymer chain comprises end caps, and wherein at least a portion of the end caps comprise an alkyl substituent, wherein alkyl substituent is a methyl, ethyl, or butyl group.

3. The polyamide of claim 1, wherein the polyamide is Nylon 2, Nylon 3, Nylon 4, Nylon 6, or a protein.

4. The polyamide of claim 1, wherein the one or more additives comprise a plasticizer, an antioxidant, a nucleating agent, a clarifying agent, a caking agent, an anti-caking agent, a pigment, aflame retardant, a dulling agent, a reactive extrusion agent, a heat stabilizer, lubricants, an anti-static component, a curing agent, a blowing agent, a biocide, a filler, a reinforcement additive, or any combination thereof.

5. The polyamide of claim 1, wherein the one or more additives comprise a plasticizer, and wherein the plasticizer comprises a caprolactam, a sulfonamide, benzene sulfonamide, N-bufyl benzene sulfonamide, polyetheramines, polyvinyl acetates, polyvinyl esters, a lactam, or combinations thereof.

6. The polyamide of claim 1, wherein the one or more additives comprise a nucleating or clarifying agent, and wherein the nucleating or clarifying agent comprises a calcium carboxylate with a long carbon chain as a main component, sorbitol, benzoates, or combinations thereof.

7. The polyamide of claim 1, wherein the one or more additives comprise a slip agent, wherein the slip agent comprises a fatty acid amide, a fatty acid ester, a metallic stearate, a wax, or combinations thereof.

8. The polyamide of claim 1, wherein the one or more additives comprise a pigment.

9. The polyamide of claim 1, wherein the one or more additives comprise a flame retardant, and wherein the flame retardant comprises short, medium, long chain chlorinated paraffins (SCCP / MCCP / LCCP), boric acid, a brominated flame retardant.a phosphorous flame retardant, a phosphate ester, a halogenated phosphate ester, a halogenated hydrocarbon, antimony oxide, aluminum oxide trihydrate, zinc borate, an ammonium orthophosphate, ammonium sulfamate, bromine and / or phosphorus containing polyol, a halogenated phenol, tetrachlorophthalic anhydride, a phosphonate ester, dibromoneopentyl alcohol, or any combinations thereof.

10. The polyamide of claim 1, wherein the one or more additives comprise a dulling agent.

11. The polyamide of claim 1, wherein the one or more additives comprise a reactive extrusion agent.

12. The polyamide of claim 1, wherein the one or more additives comprise a heat stabilizer, and wherein the heat stabilizer comprises a mixed metal salt, an organotin compound, a lead compound, an alkylorganophosphites, epoxy compound, a beta diketone, cuprous iodide, potassium iodide, a phenolic antioxidant, an aromatic amine, copper or mantoquita, KI, KBr, or any combinations thereof.

13. The polyamide of claim 1, wherein the one or more additives comprise a lubricant.

14. The polyamide of claim 1, wherein the one or more additives comprise an antistatic compound, wherein the antistatic compound comprises a metallic fiber, a metallic powders, a metallic flakes, a metal-plated polymeric material, a conductive carbon, or any combination thereof.

15. The polyamide of claim 1, wherein the one or more additives comprise a curing agent, wherein the curing agent comprises 4,4’- diaminodiphenylmethane (MDA); 2,2’- dichloro-4,4’-methylenedianiline (MOCA); Formaldehyde - reaction products with aniline; hydrazine; l,3,5-Tris(oxiran-2-ylmethyl)-l,3,5-triazinane-2,4,6-trione (TGIC) / l,3,5-tris[(2S and 2R)-2,3-epoxypropyl]-l,3,5- triazine-2,4,6-(lH,3H,5H)- trione (0-TGIC), or any combinations thereof.

16. The polyamide of claim 1 , wherein the one or more additives comprise a blowing agent.

17. The polyamide of claim 1, wherein the one or more additives comprise a biocide, wherein the biocide comprises formaldehyde, methanol, sodium hypochlorite, acetaldehyde, glyoxal, succinaldehyde. glutaaldehyde, 2-propenal. dialdehyde phthalate, glutaaldehyde, benzyl alcohol mono (poly) -hemiformal, ethylene glycol hemiformal (EGHF), [1,2-ethanediylbis (oxy)]-bis-methanol, tetrahydro-1,3, 4,6- Tetrakiss (hydroxylmethyl) imidazole [4,5-d] imidazole-2,5 (1H, 3H)-dione, orthophenylphenol (OPP) ), 2-Methyl-4-isothiazolin-3-one (MIT), 5-chloro-2-methyl- 2H-isothiazohn-3-one (CIT), l,2-benzoisothiazolin-3-one (BIT), Or a mixture thereof.The biocide may be a combination of 2-methyl-4-isothiazolin-3-one (MIT), 1,2- benzoisothiazolin-3-one (BIT), or any combination thereof.

18. The polyamide of claim 1, wherein the one or more additives comprise a filler or reinforcing agent, and wherein the filler or reinforcing agent comprises glass, carbon, aramide, calcium carbonate, talk, clay, zinc oxide, glimmer, metal powder, wood powder, asbest, barium sulphate, glass microspheres, silicious earth, or any combination thereof.

19. A method of forming a polyamide composition, the method comprising: providing a polyamide, wherein the polyamide comprises a plurality of amide groups in a backbone structure of the polyamide; modifying a portion of the plurality of amide groups in the backbone structure with one or more alkyl substituents to form the polyamide composition, wherein the polyamide has a substitution of the amide units in an amount of between about 0.1% to about 10% of the amide units in the backbone; and incorporating one or more additives into the polyamide.

20. The method of claim 19, wherein the polyamide composition has a formal of:where R comprises an alkyl substituent on an amide group of the plurality of amide groups.

21. The method of claim 19, wherein the polyamide composition has the following formula:where n is between 200 and 100,000, m is 1-11, and any of Ri, R2, and R3 can comprise a hydrogen or an alkyl substituent.

22. The method of claim 19, wherein the one or more additives comprise a plasticizer, an antioxidant, a nucleating agent, a clarifying agent, a caking agent, an anti-caking agent, a pigment, a flame retardant, a dulling agent, a reactive extrusion agent, a heat stabilizer.lubricants, an anti-static component, a curing agent, a blowing agent, a biocide, a filler, a reinforcement additive, or any combination thereof.

23. The method of claim 19, wherein the one or more additives comprise a plasticizer, and wherein the plasticizer comprises a caprolactam, a sulfonamide, benzene sulfonamide, N-butyl benzene sulfonamide, polyetheramines, polyvinyl acetates, polyvinyl esters, a lactam, or combinations thereof.

24. The method of claim 19. wherein the one or more additives comprise a nucleating or clarifying agent, and wherein the nucleating or clarifying agent comprises a calcium carboxylate with a long carbon chain as a main component, sorbitol, benzoates, or combinations thereof.

25. The method of claim 19, wherein the one or more additives comprise a slip agent, wherein the slip agent comprises a fatty acid amide, a fatty acid ester, a metallic stearate, a wax, or combinations thereof.

26. The method of claim 19, wherein the one or more additives comprise a pigment.

27. The method of claim 19, wherein the one or more additives comprise a flame retardant, and wherein the flame retardant comprises short, medium, long chain chlorinated paraffins (SCCP / MCCP / LCCP), boric acid, a brominated flame retardant, a phosphorous flame retardant, a phosphate ester, a halogenated phosphate ester, a halogenated hydrocarbon, antimony oxide, aluminum oxide trihydrate, zinc borate, an ammonium orthophosphate, ammonium sulfamate, bromine and / or phosphorus containing polyol, a halogenated phenol, tetrachlorophthalic anhydride, a phosphonate ester, dibromoneopentyl alcohol, or any combinations thereof.

28. The method of claim 19, wherein the one or more additives comprise a dulling agent.

29. The method of claim 19. wherein the one or more additives comprise a reactive extrusion agent.

30. The method of claim 19, wherein the one or more additives comprise a heat stabilizer, and wherein the heat stabilizer comprises a mixed metal salt, an organotin compound, a lead compound, an alkylorganophosphites, epoxy compound, a beta diketone, cuprous iodide, potassium iodide, a phenolic antioxidant, an aromatic amine, copper or mantoquita, KI, KBr, or any combinations thereof.

31. The method of claim 19, wherein the one or more additives comprise a lubricant.

32. The method of claim 19, wherein the one or more additives comprise an antistatic compound, wherein the antistatic compound comprises a metallic fiber, a metallicpowder, a metallic flakes, a metal-plated polymeric material, a conductive carbon, or any combination thereof.

33. The method of claim 19, wherein the one or more additives comprise a curing agent, wherein the curing agent comprises 4,4’- diaminodiphenylmethane (MDA); 2,2’- dichloro-4,4’ -methylenedianiline (MOCA); Formaldehyde - reaction products with aniline; hydrazine; l,3,5-Tris(oxiran-2-ylmethyl)-l,3,5-triazinane-2,4,6-trione (TGIC) / l,3,5-tris[(2S and 2R)-2,3-epoxypropyl]-1.3,5- triazine-2.4.6-(lH,3H,5H)- trione (P-TGIC), or any combinations thereof.

34. The method of claim 19, wherein the one or more additives comprise a blowing agent.

35. The method of claim 19, wherein the one or more additives comprise a biocide, wherein the biocide comprises formaldehyde, methanol, sodium hypochlorite, acetaldehyde, glyoxal, succinaldehyde, glutaaldehyde, 2-propenal, dialdehyde phthalate, glutaaldehyde, benzyl alcohol mono (poly) -hemiformal, ethylene glycol hemiformal (EGHF), [1,2-ethanediylbis (oxy)]-bis-methanol, tetrahydro- 1,3, 4,6-Tetrakiss (hydroxylmethyl) imidazole [4,5-d] imidazole-2,5 (1H, 3H)-dione, orthophenylphenol (OPP) ), 2-Methyl-4-isothiazolin-3-one (MIT), 5-chloro-2-methyl-2H-isothiazolin-3- one (CIT), l,2-benzoisothiazolin-3-one (BIT), Or a mixture thereof. The biocide may be a combination of 2-methyl-4-isothiazolin-3-one (MIT), l,2-benzoisothiazolin-3-one (BIT), or any combination thereof.

36. The method of claim 19, wherein the one or more additives comprise a filler or reinforcing agent, and wherein the filler or reinforcing agent comprises glass, carbon, aramide, calcium carbonate, talk, clay, zinc oxide, glimmer, metal powder, wood powder, asbest, barium sulphate, glass microspheres, silicious earth, or any combination thereof.

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