Definitions

• the present invention relates to a process for manufacturing a polyamide resin composition. Specifically, it relates to a manufacturing process which comprises adding a heat stabilizer to improve the heat stability and the weathering resistance of a polyamide and, at the same time, to suppress any significant change in color of the polyamide. Incorporating an effective copper compound into a polyamide composition for improving the heat resistance and weathering resistance of the polyamide composition is a well-known method for preventing thermal oxidative degradation of said composition. Additives can be added to polyamide compositions at any stage before molding the polyamide composition into molded article.
• one of the methods used to incorporate an additive into a polyamide composition involves dry blending the polyamide with the additive, followed by melt mixing and extruding the dry-blended product into pellets.
• Another known method for compounding an additive into a polyamide composition is to prepare master polyamide pellets, followed by blending these master pellets with dilution polyamide pellets.
• a copper-type heat stabilizer may be incorporated into a polyamide composition by adding the heat stabilizer to a polyamide containing no heat stabilizer via an extruder or by adding the heat stabilizer to the polyamide during its polymerization.
• a comparison of the two methods shows that the latter provides a product with better color compared to the former so that heat stabilizers are, in general, added to polyamides during the polymerization thereof.
• yellowing it is meant the extent of yellowing experienced by a molded polyamide article, said yellowing being expressed by the value YI-C.
• the YI-C is measured on a sample of pellets or plates with an area of at least 5 cm x 5 cm. Pellets in a glass cup are used for measurement. The measurement is possible with an area less than this range, but precision drops. The measurement is made by a differential color meter.
• the relationship between YI-C and color in terms of the absolute coordinates (X, Y, Z coordinates) is given for the following formula:
• a pigment or coloring agent is normally added for coloring the molded article.
• coloring the molded article to the desired color will require greater amounts of pigments or coloring agents. If a colored resin as obtained is to be colored in a different color, an inorganic pigment, such as titanium oxide, must be incorporated in large amounts.
• the present invention relates to a process for manufacturing a polyamide composition molded article comprising the steps of (a) preparing a polyamide composition masterbatch containing a high content of a heat stabilizer by compounding a polyamide resin with a heat stabilizer, (b) melt-mixing, extruding, and pelletizing the masterbatch with heating into master pellets, (c) mixing these master pellets with a dilution polyamide resin so as to generate a mixture with a heat stabilizer content falling within a range of which is needed for heat stabilization of a polyamide composition, and (d) melt molding into articles under required heating.
• the process of this invention permits the manufacture of a polyamide composition molded article with much less yellowing than would be expected from the content of the heat stabilizer in the polyamide composition molded article.
• the polyamide composition molded article obtained by the process of this invention has a much lower degree of coloration (or yellowing) than the degree of coloration which would be expected from the amount of heat stabilizer present in the composition.
• Such considerable improvement in terms of coloration may be rationalized by the fact that the yellowing capability of the heat stabilizer towards the polyamide resin is completely or mostly consumed during the preparation of master pellets, so that by the time it is compounded with a dilution polyamide, the heat stabilizer no longer has any remaining yellowing capability toward the dilution polyamide resin.
• a coloration mechanism is based on simple speculation and this coloring mechanism should in no way give a limiting interpretation to the present invention.
• the polyamides used in the present invention are well known in the art and are commercially available.
• the polyamide is a high molecular weight material in which hydrocarbon groups or hydrocarbon groups interrupted by oxygen or sulfur are hnked together by amide bonds. It has a molecular weight of at least 5,000 in order to exhibit any moldability. It includes a material generally called "nylon".
• polyamide useful herein may be one prepared from a linear diamine represented by the formula
• these polyamides may be prepared also from said amines and amide-forming derivatives of these acids, such as esters, acid chlorides, amine salts, and the like.
• dicarboxyhc acids used for manufacturing these polyamides include adipic acid, pimelic acid, suberic acid, sebacic acid, and dodecane dicarboxyhc acid, while typical diamines include hexamethylene diamine and octamethylene diamine.
• Other polyamide types useful herein include those prepared by condensing an omega-amino carboxylic acid represented by the formula
• x is an integer of 3-12, or intramolecular amides thereof.
• polyamides which may be useful herein are polyamides in which part of the diamine components are replaced by any of bis(3-aminopropyl)ether, bis(aminomethyl)cyclohexane, metaphenylene diamine, metaxylylene diamine, and 4,4-diaminodiphenylether, with part of the dicarboxyhc acid components being replaced by any of isophthalic acid, terephthalic acid, and the like.
• polyamides useful herein include polyhexamethylene adipamide (Nylon 66), polyhexamethylene azelamide (Nylon 69), polyhexamethylene sebacamide (Nylon 610), polyhexamethylene dodecanoamide (nylon 612), polycaprolactam (Nylon 6), polylauryl lactam, poly-11-amino-undecanomide, and bis-(paraamino-cyclohexyl) methane dodecanoamide.
• polyamides which can be used are those copolymers from two types selected from the above polymers or those obtained by terpolymerization of the above polymers or their components (for example, polymers prepared from adipic acid and isophthalic acid and hexamethylene diamine).
• Typical heat stabilizers useful in the present invention include, for example, Group I metal halides (such as halides of sodium, potassium, lithium, and cuprous copper, for example), chlorides, bromides, iodides, sterically-hindered phenols, hydroquinones, derivatives of the compounds of these groups, and mixtures thereof.
• Group I metal halides such as halides of sodium, potassium, lithium, and cuprous copper, for example
• chlorides bromides, iodides, sterically-hindered phenols, hydroquinones, derivatives of the compounds of these groups, and mixtures thereof.
• the present invention may also incorporate a combination of UV stabilizers with these heat stabilizers where the typical UV stabilizers include various substituted resorcinols, salicylates, benzotriazoles, benzophenones, and the like.
• the heat stabilizer is first compounded with a polyamide composition, then melt mixed, extruded, and pelletized into master pellets.
• the amount of heat stabilizer used for incorporation into the polyamide composition should be adjusted so that when these master pellets are mixed with a dilution polyamide resin, the resultant mixture has a heat stabilizer content within the range typically necessary for heat stabilizing the mixture.
• the amount of copper ions in the mixture of master pellets and dilution polyamide resin is preferably in the range of 30-200 ppm.
• the heat stabilized masterbatch (master pellets) can be diluted to any extent with the polyamide dilution resin where the effect of decreasing yellowing in a resultant molded article is greater with a higher dilution ratio.
• An advantageous effect is particularly recognized where the masterbatch is diluted by at least 50% with the dilution polyamide resin (see Figure 2).
• the masterbatch is diluted too much (for example, wherein the amount of the masterbatch in the final mixture is 1% or less)
• a dilution ratio of about 2 Le. . 50% of the masterbatch in the final mixture) will increase the cost of production.
• the preferred dilution ratios are from 4 to not more than 100 (1% to 25% in terms of the amount of the masterbatch in the final mixture).
• compositions of this invention may contain, in addition to stabilizers against oxidation, heat, and UV-degradation, common additives, such as inhibitors, lubricants, mold release agents, coloring agents (including dyes and pigments), fibrous or granular filler, reinforcing agent, plasticizer, and the like. These additives are normally added commonly in the mixing stages.
• the heat stabilizer (HS) used in this example was a mixture of copper iodide and potassium iodide. The mixing ratio of the heat stabilizer used in the test was kept constant.
• the master chips had compositions as given in Table 1. below.
• the nylon 66 master chips prepared in the above step i) were used to prepare test pieces. Test pieces where extruded from the same twin screw extruder as that used in the preparation of these master chips, with no dilution for master chip 1-1 (100% masterbatch content); by mixing with the same amount of additive-free nylon 66 pellets (dilution ratio 2) (50% masterbatch content) for master chip 1-2; mixing with three times the amount of additive-free nylon 66 pellets (dilution ratio of 3) (25% masterbatch content) for master chip 1-3; mixing with nine times the amount of additive-free nylon 66 pellets (dilution ratio 9) (10% masterbatch content) for master chip 1-4; and mixing with 19 parts by weight of additive- free nylon 66 pellets (dilution ratio of 19) (5% masterbatch content) for master chip 1-5, followed by measuring YI-C for these samples. The content of copper ions in each sample was held at a constant level of 150 ppm by
• YI-C measurement are given in Figure 2 and Table 2. below.
• Figure 2 shows that for the masterbatch content of 100%, a molded test piece from a master chip 1-1 alone had a YI-C value of 28.
• the test piece At a masterbatch content of 50% (that is, a molded test piece obtained from master chip 1-2 diluted at a dilution ratio of 2), the test piece had a YI-C value of 26.
• a masterbatch content of 25% that is, a molded test piece obtained from master chip 1-3 diluted at a dilution ratio of 3
• the test piece had a YI-C value of 18.
• the test piece had a YI-C value of 16.
• the test piece had a YI-C value as low as 15, which is about half the value of the 100% masterbatch content.
• Example 2 Master chip 1-1 of Example 1, without dilution, and master chip 1-4 mixed with nine times the amount of additive-free nylon 66 chips (dilution ratio of 9) were melt extruded. The change in time of the tensile strength was measured on the extrudates for these two samples and is reported in Figure 3.
• Figure 4 shows that the incorporation of the additive in the form of a master chip to a nylon resulted in only a slight decrease in elongation. Although there is a drop in elongation with the passage of time, the tendency for reduction is identical to that obtained with a molded article from master chip 1-1 alone.
• Figure 1 A graph which shows a relationship between the amount of a copper compound added to a polyamide and the yellowing of the polyamide, in terms of YI-C values.
• FIG. 2 A figure which shows the relationship between the masterbatch content and the YI-C value, with the copper ion content as the heat stabilizer held at a constant level of 150 ppm.
• Figure 3 A figure which shows a relationship between tensile strength and a change with time for a sample containing 100% masterbatch and a sample containing 10% masterbatch.
• Figure 4 A figure showing elongation of a 100% masterbatch sample and a 10% masterbatch sample and the change with the passage of time.

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• 1993
  • 1993-10-29 EP EP94900465A patent/EP0746453A1/de not_active Withdrawn

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