IE55477B1 - Acid halide functional materials - Google Patents

Description

b a -i i < This invention relates to acid halide 5 functional materials obtained by the reaction of a hydroxyl-containing material with an acid halide which has di- or multi- halide functionality. More particularly, this invention relates to acid halide functional materials which can be employed in the 10 preparation of nylon block polymers.

Polymers containing polyamide segments and segments of another material have been disclosed in the art and are herein referred to as "nylon block 15 polymers". A combination of polyamide segments and segments of another polymeric material allows for the obtaining of block polymers with unique combinations of properties. The properties can be varied by varying the polyamide and/or other polymeric segments 20 in the block polymer. Such block polymers have been found particularly suitable for use as fibers, fabrics, films and molding resins.

In u.S. Patents 4,031,164, issued June 21, 1977, and 4,223,112, issued September 16, 1980, both to Hedrick and Gabbert, there are taught nylon block polymers containing nylon segments derived from lactam 5 monomers and other polymeric blocks derived from polyols. Polyacvl lactams provide linkages for blocks in the nylon block polymers taught in Hedrick and Gabhert. Molded articles having a unique combination of properties can be made from the nylon block 10 polymers taught therein.

It is taught in the aforementioned Hedrick and Gabbert patents that the preparation the block polymers taught therein involves mixing together lactam monomer, polyol, lactam polymerization catalvst 15 and the polyacvl lactam. The process described in above-referred to Hedrick and Gabbert patents for making nylon block copolymers typically results in the formation of some polyamide homolog due to the polyacyl lactams which are agyllactam containing materials, as hereinbefore defined, reacting solely with lactam monomer. It is 20 preferable to minimize any homolog since it generally causes detrimental effects such as the reduction of molding impact properties of the nylon block copolymer. The catalytic process for imide-alcohol condensation taught"'by·'Hedrick and Gabbert in USP He 30,371, reissued August 12, 1980, 25 can be employed in the preparation of the Hedrick and Gabbert nylon block polymers, jt should be noted that by this process the reaction paths shown in Columns 3 and 4 of USP No. 2,682,526 isssued June 29, 1954, to Flory occur, thus resulting in the preparation of multiple acyllactam functional material species (hereinafter defined). Furthermore, 30 reacting a polyol and polyacyl lactam in accordance with this process results in a mixture containing residual catalyst that should be removed or inactivated to reduce the potential difficulties in any subsequent preparation of nylon block copolymer moldings from said mixture.

In U.S. Patent 3,657,385, issued April 18, 35 1972 to Matzner et al, there are disclosed block polymers prepared from lactam monomer and polyarylene polyethers by anionically polymerizing the lactam monomer with a catalyst-initiator system which comprises, as the initiator or activator, one or more 40 of certain polyarylene polyethers. The particular polyarylene polyether initiators disclosed as useful have terminal groups selected from various specified groups .

Alternative methods for the preparation of nylon block polymers, for example, of the type taught in the aforementioned Hedrick and Gabbert patents, would be of interest to those skilled in the art and is an object of the present invention. Another object of this invention is to provide new materials useful as intermediates in the preparation of nylon block, polymers. These and other objects will become apparent from the following detailed description of the present invention.

In accordance with the present invention, there is provided a composition containing one or more acid halide functional materials of the formulae: 0 0 0 0 r - I r i zjo-C-R-tC-Xlg· and Z-O-C-C-X b t u wherein, X is halogen; i- a is an integer equal to 1, 2 or 3; b is an integer equal to 2 or more; r is a di- or poly-valent group selected from hydrocarbon groups and hydrocarbon groups containing ether linkages; Z is a segment of: (1) a polyetherj. (2) a polyester :ontaining polyether or polymeric hydrocarbon segments, (3) a hydrocarbon; (4) a polysiloxane; or (5) mixtures thereof; and wherein the average value of 5 for all the acid halide functional materials in said composition is greater than two.

The invention also comprises a process for the production of a composition of the invention, that comprises reacting a polyhydroxyl material Ζ-(ΟΗ)χ, wherein x is an integer equal to 2 or more with the average value of x for all the said polyhydroxyl materials being greater than 2, and Z is (1) a polyether; (2) apolyester containing polyether segments; {3) a hydrocarbon; (4} polysiloxane; or (5) mixtures thereof, with an excess of an oxalyl halide or an acid.halide material containing at least two -4- carboxylic acid halide groups, 0 II R(C-X)y, wherein y is an integer equal to 2 or more and R is a di- or poly-valent group selected from hydrocarbon groups and hydrocarbon o.rouns containing either linkages, to prodice acid halide functional materials.

The acid halide functional materials taught herein can be prepared by reacting a hydroxyl-5 containing material with an acid halide functional material containing two or more carboxylic acid halide groups 0 If (i.e. - C - halogen groups). In the reaction mixture 10 the equivalents of acid halide groups should be maintained in excess of the hydroxyl groups. In this reaction the acid halide material attaches to the hydroxyl sites in the hydroxyl-containing material through ester linkages. By-product hydrogen halide 15 results from the hydrogen and halogen which are displaced. An example of this reaction can be depicted as follows: 0 n n R'fOH) + m RfC - X) —> Acid Halide + HX x y Functional Material wherein my :>nx + 2 In the above reaction R'(0H)x is a material 20 containing two or more hydroxyl groups, i.e. x is at least 2, preferably 2 to 4. This material can be a diol, triol or a material having higher hydroxyl content. The R' group in the hydroxyl-containing material can be a hydrocarbon (preferably having a 25 molecular weight of at least 100), a polyether or a polysiloxane group. As will be explained later, the group R‘ may correspond to or become incorporated in a segment Z.

It is to be understood that, unless otherwise stated, reference .herein to "molecular weight* for polymers or polymeric segments means number average molecular weight which can be 5 determined by methods well known in the art, e.g. gel phase chromatography.

Reference herein to "polysiloxane" group or segment means a group or segment containing at least 50 percent by weight of one or more λ 10 -fSi-O)- (a siloxane unit) repeat units. In this A structure for siloxane units A can be methyl or phenyl. Polysiloxane groups or segments would % typically have present other groups, for example, ether groups with residues of lower alkyls such as 15 ethane, such groups typically being terminating groups on a chain of repeating siloxane units. These other groups may comprise up to 50 weight percent of the polysiloxane group, preferably less than 30 weight percent.

Preferred R' groups are hydrocarbon and polyether groups. Exemplary hydrocarbon groups are alkylene in the case of diols such as ethylene glycol and polymeric hydrocarbons such as a segment of polybutadiene which can be functionalized to contain 25 two or more hydroxyl groups. A polyoxypropylene segment which can be functionalized to contain two or more hydroxyl groups is an example of a polyether group.

Exemplary hydroxyl-containing materials useful in the above depicted reaction are ethylene glycol, propylene glycol, poly(oxybutylene) glycol, poly(oxyethylene) glycol, poly(oxypropylene) diol, poly(oxypropylene) triol, poly(oxypropylene) tetrol, polybutadiene diol, hydroxyl-functionalized polydimethylsiloxanes and combinations thereof, for example, block polymers of poly(oxypropylene) and poly(oxyethylene) functionalized with two or more hydroxyl groups.

The acid halide material in the 0 a above-depicted reaction, i.e. R-fC - X) contains two or more acid halide groups, i.e. y is greater than 1, generally 2, 3 or 4, preferably 2. The R group in this acid halide material is a hydrocarbon group or a hydrocarbon group containing--ether linkages (generally up to 20 weight percent ether oxygen). Preferred are hydrocarbon groups, most preferably those containing 1 to 12 carbon atoms. Even more preferred R groups are hydrocarbon groups or hydrocarbon groups having ether linkages which provide at least three successively bonded elementary atoms between any two carbonyl groups bonded to R. Examples of preferred acid halides are sebacic acid chloride and phthalic acid chloride wherein the carbonyl groups are attached thereto either in the meta- or para- position, i.e. isophthaloyl and terephthaloyl acid chloride, respectively. 0 In place of the acid halide R-(C-X)y depicted in the above reaction there may be employed an oxalyl halide i.e. a halide 7- Ο Ο it η having the structure X - C - C - X. In the above depicted structure X is halogen.

Exemplary acid halides which may be employed in the above reaction are adipoyl chloride, terephthaloyl chloride, trimesoyl chloride, trimellitic chloride, oxalyl chloride, isophthaloyl chloride, pyromelli'oyl chloride, pimeloyl chloride, glutaryl chloride, benzophenone tetracarboxylic acid chloride, oxydiacetyl chloride, oxydibenzoyl chloride, sebacic acid chloride and azelaic acid chloride.

It is to be understood that numbers designating the amount of functional groups on materials described herein (e.g. the numbers x, y and b above) would be integers for a single molecule of -8- the material. However, many of such materials, particularly polymeric materials, generally exist in mixtures or compositions containing species having varying amounts of functionality, some species possibly having an amount higher or lower than desired. For such mixtures or compositions, a number designating the amount of functional groups would represent an average of the different species and thus would not necessarily be an integer.

Essentially all of the hydroxyl groups in the hydroxyl-containing starting material are converted in the above described reaction. By providing the acid halide groups in excess of the hydroxyl groups the resulting reaction product is functionalized with acid halide groups.

The above reaction is preferably carried out in the presence of a non-interfering solvent, e.g. cyclohexane, toluene, tetrahydrofuran, or acetone to facilitate removal of the hydrogen halide which is generated. It is also possible for the reaction to proceed without the presence of a solvent with the hydrogen halide being driven off with heat, vacuum, nitrogen sweeping or the like. When a solvent is employed in the reaction, a basic material which acts as an acid scavenger to produce a by-product which is insoluble in the solvent may be employed as a convenient means for removing the hydrogen halide.

Well known acid scavengers such as tertiary amines may be employed. The above reaction can be carried out under essentially ambient conditions and will proceed even more rapidly at higher temperatures, e.g. 30° to 150°C. Precise temperature for the reaction may -9- depend upon the solvent employed. If a solvent Is employed it can be removed after the reaction by distillation.

The above-described procedure results in reaction between a hydroxyl-group of the hydroxyl-containing material and an acid halide group of the acid halide material. The following acid halide functionalized materials can thus be prepared: 0 0 0 0 wherein. and X is halogen? a is an integer equal to 1, 2 or 3; b is an integer equal to 2 or more; R is a di- or poly- valent group selected from hydrocarbon groups and hydrocarbon groups containing ether linkages; Z is a segment of (1) a polyester (preferably said polyester is not comprised solely of poly(tetramethylene terephthalate) or poly(tetramethylene isophthalate)); (2) a polyether? (3) a hydrocarbon; or (4) a polysiloxane.

The Z segment in the above Formulae I is a segment of (1) a polyester; (2) a polyether; (3) a hydrocarbon; or (4) a polysiloxane with certain provisos recited hereinbefore. The z segment for the reaction product depicted by Formulae X 15 can be the same as an R' group of a hydroxyl- functional material employed in the reaction described hereinbefore. Alternatively, the Z segment can be a segment containing two or more residues of the starting hydroxyl-containing material linked together 20 with a residue(s) of the starting cid halide material.

It is to be understood that in connection with the description of Z segments or R' groups herein, reference to polymeric segments/groups 25 embraces oligomeric segments/groups unless a specific usage precludes such interpretation. It is also to be understood that these segments/groups may be linear, branched or even star structures. -Π- A Z segment which is a segment of a polyester could be derived from the reaction of an acid halide having di- or multi- halide functionality with a hydroxyl-containing material, the groups in the hydroxyl-containing material being linked together by the acid halide through polyester linkages. Exemplary hydroxyl-containing starting materials which may be employed in such a reaction are ethylene glycol, propylene glycol, polycaprolactone diol and polyol, and polybutadiene diol. Acid halides such as those exemplified hereinbefore may be employed. Those skilled in the art would recognize a wide variety of polyester segments which may represent Z in the above Formulae I.

It should be understood that a Z segment which is a segment of a polyester would in fact contain smaller segments which fall within the other categories of possible Z segments, for example, hydrocarbon or polyether segments. As an example, a Z segment which is a segment of a polyester can be derived from a hydroxyl-containing material R'(0H)x containing a polyether group R1 and an acid halide material wheeeby two or more of the polyether groups become linked together by the acid halide material through ester linkages. The hydroxyl-containing material may be derived from a diol, triol, or polyol. A specific example of such would be the reaction product of poly(oxypropylene) triol and terephthaloyl chloride wherein a residue of the terephthaloyl chloride provides a linkage between two units derived from the -12- triol. Such polyester Z segments could be more specifically described as poly(ether-ester) segments which are a preferred type of polyester segment within the scope of the teachings herein.

Similarly, other preferred polyester Z segments are those which are the reaction product of a diol or triol which contains polymeric hydrocarbon units with an acid halide material whereby two or more of the polymeric hydrocarbon units become linked 10 together by the acid.halide material. An example of such is the reaction product of a polybutadiene diol with terephthaloyl chloride wherein two or more polybutadiene segments are linked together by the terephthaloyl chloride through ester linkages.

Polyester segments which may represent Z can vary widely in size but generally have molecular weights of at least 500. Preferred molecular weights for these segments are from about 1,000 to about 25,000. Preferred types of polyesters which contain 20 polyether or polymeric hydrocarbon segments generally contain these segments at molecular weights of from about 500 to about 4,000.

Furthermore, as will be discussed below, the properties of a nylon block copolymer prepared from an 25 acid halide functionalized material wherein the Z segment is a polyester exhibits unexpected results when the polyester contains polyether segments having a minimum molecular weight of about 2,000.

A segment of a polyether is a preferred Z 30 segment in the present invention. Such can be derived from a hydroxyl-containing material which contains a polyether segment. Such hydroxyl-containing materials which are preferred include poly(oxyethylene) glycol; -13- poly(oxybutylene) glycol? poly(oxypropylene) diol, triol, and tetrol; and block polymers of poly-(oxypropylene) and poly(oxyethylene) functionalized with two or more hydroxyl groups.

The Z polyether segments generally have a molecular weight of at least 500, preferably at least 1,000, and more preferably at least about 2,000. Preferred molecular weights are from about 1,000 to about 25,000, more preferred 2,000-25,000. Even more preferred are molecular weights from about 2,000 to about 4,000 for diol derivatives, from about 3,000 to about 12,000 for triol derivatives and from about 4,000 to about 16,000 for tetrol derivatives.

It has been determined, as will be further discussed below, that the properties of a nylon block copolymer prepared from an acid halide functionalized material wherein the Z segment is a polyether can be significantly influenced by the molecular weight of the segment and that certain preferred molecular weights result in unexpected beneficial results.

It has further been determined that a minimal amount of cross-linking in the prepared nylon block copolymer, which occurs when the average functionality of a composition of acid halide functional materials is greater than two, also results in unexpectedly improved properties. These features will be discussed and exemplified more fully below. -14- A Z segment which is a segment of a hydrocarbon can be derived from a hydroxyl-containing material which contains a hydrocarbon segment. The size of the hydrocarbon group can vary widely in size 5 from alkylene groups of low molecular weight to , polymeric hydrocarbons of substantially higher molecular weight. If Z is a low molecular weight hydrocarbon the acid halide-functional materials of Formulae I could be employed to join nylon 10 blocks together as described hereinafter. The resulting linkage would introduce the low molecular weight hydrocarbon as an additional block in the resulting nylon block polymer. Examples of low molecular weight hydrocarbon (Z) segments would be the 15 C2 to C7 alkylenes.

Preferred Z segments in the present invention are segments of polymeric hydrocarbons. By "polymeric hydrocarbon segment" herein is meant a hydrocarbon segment of molecular weight of at least 20 about 100 and containing two or more repeat units.

Exemplary hydroxyl-containing materials which can be employed to provide Z segments which are segments of a higher molecular weight or polymeric hydrocarbon are alkylene (Cg and above) glycols and polybutadiene diols, triols, tetrols and 25 even higher polyols. Segments which are polymeric hydrocarbons preferably have a molecular weight of at least 500, even more preferably from about 1,000 to about 25,000. Most preferred are molecular weights from about 1,000 to about 4,000 for diol derivatives, 30 from about 3,000 to about 12,000 for triol derivatives, and from about 4,000 to. about 16,000 for tetrol derivatives.

The Z segment may also be a segment of a polysiloxane, such being defined hereinbefore. Such a Z segment could be derived from a hydroxyl-containing material having a polysiloxane segment. Exemplary hydroxyl-containing materials of this type are polydimethylsiloxanes containing two or more hydroxyl functional groups. Polysiloxane segments would generally have a- molecular weight of at least 500, preferably at least 1,000. More preferably the molecular weight of such segments would be from about 1,000 to about 25,000.

It should be recognized that the Z segment in the above Formulae may contain a combination of the just described polyester, polyether, hydrocarbon and polysiloxane segments. As discussed hereinbefore preferred_polyester segments contain polyether or polyhydrocarbon segments. Also as discussed hereinbefore, polysiloxane segments as defined herein typically contain groups other than siloxane units.

It is recognized that other combinations of polyester, polyether, hydrocarbon and polysiloxane segments are possible, and such are contemplated equivalents for use as Z segments in the present invention.

In the above Formula X is a halogen, preferably chlorine or bromine, most preferably chlorine. The integer a in Formula I is preferably 1 which would be the case when a diacid 0 0 n * halide of the structure X-C-R-C-Xis employed in the reaction described above. The integer b in Formula I is at least 2, preferably 2 to 20, most preferably 2 to about 4. R in the above -16- Formula X is a di- or poly- valent hydrocarbon group (valency equal to a + 1) and would correspond to the Ft group in the acid halide starting material in the above described reaction scheme.

Acid halide functional materials of the present teachings which are preferred are those represented by the formulae: 0 0 n Z-0 - c n R-fC - X)a b (II) wherein X is chlorine or bromine, b is 2 to about 4 and R and Z are-as defined hereinabove. As discussed hereinabove, a further preferred form for acid halide functional materials 'is wherein the R groups provide at least three successively bonded elementary atoms between any two carbonyl groups bonded to R. Examples of such R groups are those derived from adipoyl halide, isophthaloyl halide and terephthaloyl halide.

The acid halide functional materials taught herein have been found to be useful in the preparation of nylon block polymers. It has been found that the acid halide functional materials of the present invention can be reacted with a lactam monomer as described in our Irish Patent Application No. 1422/82 to result in an acyllactam funtional material which can further be reacted with lactam monomer to form a nylon block polymer as described in our Irish Patent No. 54045. For example, the acid halide funtional materials depicted in Formula I above can be reacted with a lactam monomer containing from about 4 to about 12 carbon atoms, to produce the following acyllactam functional materials: -17- - R-fC - Q) (° and 240 0 0 n m c - C - QL (III ) wherein, 0 Q is with Y = C3-Cii alkylene; and a, b, R and Z are as defined above for Formula I The reaction of acid halide functional materials with lactam monomer to prepare the acyllactara functional materials of Formula III would typically be carried out in the presence of a solvent, e.g. cyclohexane, toluene, acetone or excess lactam monomer, and an acid scavenger to facilitate the removal of hydrogen halide generated in the reaction. The reaction may also be carried out without the presence of a solvent. The previous discussion regarding the use of solvent and reaction conditions in connection with the reaction of hydroxyl-containing material with acid halide functional material equally applies here. In an alternative method the acyllactam functional materials can be prepared under similar conditions from a reaction mixture containing a hydroxyl-containing material, an acid halide functional material and lactam monomer, without ever isolating the intermediate acid halide functional material (Formula I) which is formed. A quantitative reaction is preferred to displace essentially all of the halogens in the acid halide of Formula I with lactam groups.

The acyllactara functional polymer of Formula· III above can then be reacted with additional lactam monomer to prepare a nylon block polymer. Additional hydroxyl-containing material may be included in the reaction mixture but the acyllactam groups should be present in excess of the hydroxyl groups in the mixture. The hydroxyl-containing material will become incorporated in.the nylon block -19- polymer. The materials should be intimately mixed. Antioxidant is generally included in the reaction mix. This reaction is generally carried out in the presence of a suitable basic catalyst for the anionic 5 polymerization of lactam, preferably caprolactam magnesium bromide or chloride. A small amount of catalyst may be effective, e.g. a fraction of one mole percent of the lactam monomer to be polymerized, but higher amounts, e.g. from 1 to 20 mole percent, or 10 higher, based on the lactam monomer may be employed. The lactam monomers generally contain 4 to about 12 carbon atoms, preferably 6 to about 12. Caprolactam (which herein means ε-caprolactam) is particularly preferred. Corresponding residues of such preferred 15 lactam monomers are preferred for Q in Formula III.

In relatively short reaction times, e.g., less than 10 minutes or even less than 30 seconds, and under moderate conditions, e.g. from about 70°C to about 250°C, preferably about 120°C to about 170°C, 20 the formation of a nylon block polymer results. The lactam can polymerize at the acyllactam sites and also be inserted at ester and amide sites. Nylon block polymers disclosed in the aforementioned Hedrick and Gabbert patents can thus be prepared. The fast 25 reaction time to form the nylon block polymers makes the materials disclosed herein particularly useful in reaction injection molding applications, with other related applications, such as in-mold coating of substrates, rotation molding, resin transfer molding, 30 and pultrusion molding also contemplated.

The relative amounts of lactam monomer and acyllactam functional polymer employed in the preparation of nylon block polymer by the process -20- described above can vary widely depending upon the nylon block polymer desired. The lactam monomer and acyllactam functional polymer can be present in proportions ranging up to 99 parts by weight of either component to 1 part by weight of the other. Preferred amounts are from about 60 to about 90 percent by weight lactam monomer and from about 10 to about 40 percent by weight acyllactam functional polymer. However, from about 40 to about 70 percent by weight acyllactam functional polymer can be employed to make elastomeric block polymers. Under typical reaction conditions the polymerization is essentially quantitative, i.e. essentially all of the lactam and acyllactam functional polymer is incorporated in the nylon block polymer.

In the- preparation of nylon block polymers it may be desirable to conduct the polymerization reaction in the presence of one or more other materials conventionally incorporated in nylon block polymers. Such materials would include fillers, plasticizers, flame retardants, stabilizers, fibrous reinforcing agents such as asbestos and glass fiber, dyes and pigmenting materials. Such materials may be introduced in the materials of Formula I or III taught herein, or otherwise.

The following examples will illustrate the present invention in greater detail. These examples are for illustrative purposes only and are not to be construed as limiting the scope of the invention which would include various other modifications. Unless otherwise indicated herein, all parts, percentages, ratios and the like are by weight. -21- EXAMPLE 1 A. Preparation of Acid Halide Functional Material A solution of 48.2 grams (.049 equivalents) Plutacol GP-3030 (polyoxypropylene triol, Mol. Wt. about 3,000) in 40 cc. toluene was refluxed to remove essentially all water by azeotrope. The mixture was cooled to room temperature, and 9.45 grams (0.103 equivalents) of crude adipoyl chloride was added. The solution was heated to reflux. During reflux hydrogen chloride gas was evolved rapidly. The mixture was refluxed one hour.

This reaction resulted in the hydroxyl sites of the polyoxypropylene triol being functionalized by the adipoyl chloride to form the tri (acid chloride) functional derivative.

B. Preparation of Acyllactam Functional Material To the resulting reaction product prepared in A. above was added 169 milliliters (mis.) dry molten caprolactam. The mixture was refluxed. Reflux pot temperature rose to 185°C. Hydrogen chloride evolution occurred at a moderate rate. The course of reaction was monitored by periodic determination of residual acidity. After one and one-half hours reflux at 185°C., acidity was .077 milli-equivalents/gram (meq./gm.). The solution was cooled and was allowed to set overnight. An additional 45 mis. toluene was added and the solution again refluxed - this time at 140° pot temperature. After two hours additional reflux (total reflux time = three and one-half hours) acidity was .042 meq./gm. when titrated to phenolphthalein end point with 0.1 normal sodium hydroxide. Additional reflux period of three and one-half hours did not change this acidity.

This reaction resulted in the chlorine atoms in the product prepared in A. being displaced by caprolactam groups to form the tri(acyllactam) functional derivative.

C. Preparation of Nylon Block Po.lymer To the reaction product prepared in B. above an additional 11.8 grams Pluracol GP-3030 were added. Toluene was stripped off under vacuum, and then 25 cc. caprolactam removed by distillation. The resulting solution was cooled to 75°C. and 84 mis. of 0.4 molar bromomagnesium caprolactam (in caprolactam) was injected under vacuum. The mixture was stirred vigorously for 20 seconds, the vacuum released to nitrogen and the mixture poured into a 130°C. Teflon-lined mold. The material was set into a firm polymer in two minutes. After an additional two minutes the polymer was removed from the mold and cut into specimens for physical testing. The resulting polymer was a nylon block copolymer which contained about 20% poly(oxypropylene) and which exhibited the following properties (determined in accordance with the procedures described hereinafter for Examples 29-51): Tensile Strength Tensile Elongation Tear Strength Flexural Modulus Notched Izod Impact 5960 (psi) 41 MPa 30% 1280 (pli) 224 x 103 N/m 157,000 (psi) 1082.5 MPa 6.6 (ft. lbs./in). 352 J/m The following polyols and acid halides were employed in the preparation of additional acid halide functional polymers, acyllactam functional polymers and nylon block polymers: -23- TABLE A Designation Niax 11-34 (NIAX) Pluracol P-380 (P380) Pluracol GP 3030 ' (GP) Pluracol P494 (P494) Carbowax 4000 (CARB) R 45 M * (R45) Polyol Mix (MIX) Q4-3667 ** (Q4) Tetrol 9000 (TET 9) Triol 8000 (TRI 8) Polyols Description - Ethylene Oxide capped poly(oxypropylene) triol (Molec. Wt. about 4,800) . - Poly(oxypropylene) triol (Molec. Wt. about 5,760). - Poly(oxypropylene) triol (Molec. Wt. about 3,000). - Poly(oxypropylene) tetrol (Molec. Wt. about 4,750). - Poly(oxyethylene) diol (Molec. Wt. about 3,700). - Poly(butadiene) diol (Molec. Wt. about 2,800). - 50/50 by mole mixture of Niax 11-34 and GP 3030. - Silicone polycarbinol. - Ethylene Oxide capped poly(oxypropylene) tetrol (Molec. Wt. about 9,000). - Ethylene Oxide capped poly(oxypropylene) triol (Molec. Wt. about 8,000). a! * Arco R45M is a Trade Mark ** Dow Corning Q4-3667 is a Trade Mark -24- TABLE B ACID HALIDES Designation Terephthaloyl Chloride TERE Adipoyl Chloride ADIP Isophthaloyl Chloride ISOP ISOP/TERE ISO/TER Mixture (50/50 Wt. %) Oxydibenzoyl Chloride OBC Oxalyl Chloride OXA -25- EXAMPLE 2 Preparation of-Acld Halide Functional Material A solution of 96.0 grains (0.02 mole) of Niax 11-34 in 237 mis. of cyclohexane was dried by removing 27 mis. of the water azeotrope during a half-hour reflux period. The solution was cooled to 21°C. and 12.18 grams (0.06 mole) of terephthaloyl chloride (TERE) were added with stirring. A solution of 6.08 grams (0.06 mole) of triethylamine in 20 milliliters of cyclohexane was added over 5 minutes. The temperature rose from 21°C. to 26°C., and a white precipitate formed. The solution was heated to reflux and was cooled immediately to 10°C. and filtered through "Celite". Removal of the solvent under vacuum at 80°C. left 102.48 grams of a yellow syrup. The IR spectrum showed ester and acid chloride carbonyl absorption at 1745 cm.-* and 1800 cm.-*, respectively, and no hydroxyl absorption, demonstrating the formation of the desired acid halide functional polymer.

EXAMPLE 3 A. Preparation of Acid-Halide Functional Material A solution containing 48.0 grams (0.01 mole) of Niax 11-34 in 77 mis. of cyclohexane was dried by removing 27 mis. of the water azeotrope during a half-hour reflux. The polyol solution was cooled to 50°C., and 6.09 grams (0.03 mole) of solid terephthaloyl chloride (TERE) were added with stirring. A solution of 3.04 grams (0.03 mole) of dry triethylamine in 20 mis. of cyclohexane was added over a period of 10 minutes. The temperature rose from 47.5°C. to 49°C. The resulting creamy slurry was stirred and heated at reflux for a half-hour to -26- complete formation of the acid halide functional polymer, B. Preparation of-Acyllactam-Functional Material The reaction mixture from A. above was cooled to 42°C. and 4.0 grams (0.035 mole) of solid caprolactam were added with stirring. A solution of 3.54 grams (0.035 mole) of triethylamine in 20 mis. of cyclohexane was added over a period of seven minutes. The temperature rose 42°C. to 53°C. An additional 60 mis, of cyclohexane were added, and the mixture was heated at reflux with stirring for a half-hour.

Cooling to 11°C. and filtration through "Celite" left a clear, colorless filtrate. Removal of the solvent at 80°C. under vacuum for three hours yielded 52.26 grams of a clear, yellow syrup. The acidity of the resulting acyllactam functional polymeric material was 0.028 megt/gm.

EXAMPLE 4 Preparation Of-Acyllactam-Functional Material A solution of 96.0 grams (0.02 mole) of Niax 11-34 and 7.0 grams (0.062 mole) of caprolactam in 227 mis. of cyclohexane was dried by refluxing for an hour, while 27 mis. of the water azeotrope were removed. The solution was cooled to 15°C., and 12.18 grams (0.06 mole) of terephthaloyl chloride (TERE) were added with stirring. A solution of 12.66 grams (0.125 mole) of triethylamine in 40 mis. of cyclohexane was added over a five minute period. The temperature rose from 15°C. to 30°C., and a white precipitate formed. The mixture was heated to reflux and kept there for one hour; then, 1.5 grams of methanol were added and refluxing was continued for another hour. The mixture was cooled to 10°C. and was -27- filtered through "Celite*. Removal of the solvent under vacuum at 80°C. over three hours left 93.93 grams of an amber syrup. The acidity of the resulting acyllactam functional polymeric material was 0.032 meq./gm.

EXAMPLES 5-28 Additional Examples 5-28 were carried out substantially in accordance with previous Example 3 (A and 8) or. Example 4 except for the particular materials and amounts thereof which were employed.

The type and amounts of materials and method of preparation (Ex. 3 or Ex. 4) for each of Examples 5-28 are shown in Table C. In some of the Examples run in accordance with Example 3, the reflux in Step B was extended beyond 30 minutes, up to 3 hours in some cases. Additiohally, in some of the Examples run in accordance with Example 3 a small amount of methanol or of anhydrous sodium carbonate was added after 30 to 60 minutes of reflux in Step B for the purpose of adjusting the acidity of the final product. For some of the Examples run in accordance with Example 4 an equivalent amount of sodium carbonate was used instead of the methanol added during the reflux step. The acidity of the resulting acyllactam functiona. material was between about 0.028 and 0.3 meq./gm. for each of these examples. -28- Ό Ο η γο η ΓΟ η ro m η Γθ m ΓΟ η Λ Φ X X X X X X X X X X X X X Σ ω ω ω 03 ω ω 03 ω ω ω ω 03 ω * .η ιη m ιη ιη ιη CM Η ιη ιη ιη m «, 0) VO ιο CN νο νο CM νο <Ν <Ν ηί C0 ιη 03 «C Μ ο ο ιΗ ο ο rH *Η ιΗ *-η Η ο ρ- rH οί Ο * • • • • • • • • • • * • £*« Σ ο ο Ο ο ο Ο Ο Ο Ο Ο ο Ρΐ Ο ο η rH ιη Ν ιη ιη CM CM rH ιη m ιη ιη 10 ο ro η νο η η νο οσ νο νο νο κΤ ιη 9) Η Η Ο ο ο ο ο σ ο Ο ο ο Ο <3V σ ο Ο • • • • • • • • * • • * W £ Ο ο σ ο ο ο ο Ο ο ο ο rH ο a r m » υ *** r·*· 0) «>»* r* r» © 41 m C0 νο cn m VO CO VO VO VO «a· Ο © rH ο ο o o o o o o o o © © Q ο • • • • * 0 • Λ • • • • • ί ο ο o o o o o © o o © rH O "or· *-» *— 'T" '-r w w V 4) ω Ό u3 •*4 0) rH < « o: S ω e <Ό ω ω to to 0* 0« 0« ω \ 03 ω os 03 wH CC C£ £ « w o M 2 o ee « (2 © Ο ω CO w u Q to Q Ό to ω ω 01 03 < ε- fr* fr· 6h nC M 4j £*« M 5- Η t- e* m ,τν *·*. CM n _ _ rH ΓΗ rH rH η CM rH CM CM CM Ο «i rH © Ο © Ο ο Ο Ο Ο Ο Ο νο Ο H O • • • • • • • « • • • O © ο Ο ο Ο © ο Ο ο Ο ο Ο £· o *— •W* *>-* ·—* w w w rH O > X X X X ΤΓ X © X ιη rH < < < < σ» Ον < X CC < 0 M CU Μ 0« Μ Μ *3* Μ Η < ΗΗ os a* z u ζ ο ζ ζ α & Ζ X υ Ζ 41 Η α Β ιϋ X 03 Ο ΙΠ Η ·"* ιη VO Ρ* C0 Ν Λ in \θ > -29· Ό O Ν' KJ> oft ΤΓ V m Λ 4-> 0) X X X X X X X Σ ω a W ω &} W ω w in in N .m in in in ** ε fft υ (ft 04 Of Of 04 04 04 Φ m © (ft «>·»· -*ί. *»«, ιΛ © ID ID © ID ID ID σι pH O o o O O o O o , Cl • • • • « • Ό s o O o O © o o © *-"· r c φ 0 Ό u ·<-< H υ <0 £ ω Ό ω &3 ω S ω ω © cc a: —» *« © Preparation-of Nylon Block Polymers Nylon block polymers were prepared from acyllactam functional polymers prepared in Examples 5 5-28 by either a hand casting polymerization method (HC) or a reaction injection molding polymerization method (RIM). These methods are described below.

A. Hand 'Casting--of-Nylon -Block Polymers (Examples 29-47).

In a 500 ml, flask ecjipped with stirrer, thermocouple and nitrogen inlet were charged caprolactam and a prepolymer which was an acyllactam-functional polymer prepared in accordance with one of the earlier Examples 5-28. The specific 15 prepolymer example and the amount of materials employed^in each of Examples 29-47 is shown in Table *> D. in each case 1.5 grams of Flectol H (an antioxidant sold by Monsanto Company which is polymerized l,2-dihydro-2,2,4-trimethylquinoline) was 20 added to the charge. The mixture was heated under vacuum to distill 25 mis. caprolactam and then cooled to 75°C.

Separately prepared was a catalyst solution which was a solution of bromomagnesiura 25 caprolactam in caprolactam. The catalyst solution was generally prepared by adding a solution of 3 molar ethyl magnesium bromide in diethyl ether to dry caprolactam followed by thorough degassing under vacuum. Catalyst solutions of various molarities were 30 prepared. For example, a 0.5 molar bromomagnesium caprolactam catalyst solution was prepared by adding 17 mis. of 3 molar ethyl magnesium bromide in diethyl ether to 100 grams of dry caprolactam with degassing * Trade Mark -31- as stated above. The molarity of the catalyst solution employed for specific examples is indicated in Table D.

To the above prepared prepolymer solution 5 was injected a specified amount of catalyst solution under vacuum. The specific amount of catalyst solution employed for the Examples 29-47 is shown in Table D. "After stirring vigorously for fifty seconds the vacuum was released to nitrogen and the catalyzed 10 mixture was poured into a Teflon-lined mold heated to 130°C. After 5 to 15 minutes in the mold the resulting solid nylon block polymer was removed. The polymerization of the prepolymer and caprolactam was essentially quantitative in the formation of the nylon 15 block polymer. Specimens were cut for testing. -32- m ο ο to η m <λ"* μ 4J 4J| S to 4J3ι &- ω.η £ <Λ 1/1 <0 οι Ό <υ 10 0 C0 Ο Ό λ η λ ς· 0 ιΛ \Γί m ΙΛ tn ιη ιΛ ΙΛ • • • • • * • • Ο Ο ο Ο ο ο Ο Ο Cι.οο 01ε Ν γΗο 04 _* οο ε 5 Ο Λ C1 JJ S C 0. 10 0 η «3 α> CO Η 10 C0 03 σι rH rH ε rH γ** Ο rH Γ* m ΓΟ Ν \ iS *0 Ο *-η Η rH (Η Η rH rH Μ rH 0 V* U (3 α oa Ό cn <0 Γ* 0) ω t ο rH ϋ uj rH U & Μ CL· 0 £ UH < C s • c χ 3 0) w •H ω Ο ε B (V ε 5J ΓΜ *CT «Η η· C0 σ» u ο < Η • • ♦ • • • • S Ο ιο tn Ν' Ο η *3* VD rH U) α «τ η Γ- cn νη *Τ Γ- to 1 0 <0 Wi Ό rH 9 ο« 0) C CP ω H r-» U to • α3 V 4J HJ < ε c S ε* & 4) 0 w Η Η o 0 α <*> α ε ιη 10 ί*· CO σ\ Ο Ο rH o tn ® <α rH rH rH to CH U χ rH CU ω <0 to λ* QJ Β <0 X Cd rn ·* 0) Ό rH 0) & XJε ΓΗ β\ΟΗΝ(η^·Λ0 cHmmtnmmtncn <0 Xω 33- 0} £ IDin tnmoj.ommooQj^nmniricatfl <91 HI o|s| in m m in in in m in ID • • • « • • • • • Ο ο ο ο ο ο ο ο Ο £ <9 JJ t) e H < O a E O •t— -P E QJ > C « 05 Ο Ο m νο 05 ιη σ» 'ί ID Ο Γ-» σι r*» ID m ιο Η CM <η Η Μ Η Η f-i Ή +» ca) to Φ 5-α. 1. V i—1 rH a o ε a Λ a X u a· ω TJ a «ΙΰΗΝΜς· Η Η N N N N *o E flj 0) i—i a £ <0 X Ci3 K *in kn r~ in o Ή 34- B. Reaction Injection Holding of Nylon-Block Polymers (Examples 48-51).

In a 500 ml. flask equipped with stirrer, thermocouple and nitrogen inlet were charged 5 caprolactam and a prepolymer which was an acyllactam functional polymer prepared in accordance with earlier Examples 5-29. The specific prepolymer example and the amount of materials employed in preparing the prepolymer solutions in each of Examples 48-51 is 10 shown in Table E. To each charge was added 1.5 grams * of Flectol H. The mixture was dried by heating under vacuum to distill 25 mis. caprolactam and then cooled to 75°C.

Separately a catalyst solution consisting of 15 bromomagnesium caprolactam in caprolactam was prepared by adding a solution of 3 molar ethyl magnesium bromide in diethyl ether to dry caprolactam followed by thorough degassing under vacuum. For example, a 0.26 molar bromomagnesium caprolactam catalyst 20 solution was prepared by adding 17 mis. of 3 molar ethyl magnesium bromide in diethyl ether to 200 grams of dry caprolactam. Catalyst solutions of varying molarities were employed in the Examples as indicated in Table E.

A reaction injection molding was made by pumping the above solutions into a closed mold heated to 130°C. Equal amounts by volume of the prepolymer solution and the catalyst solution were combined by means of gear pumping, except for Example 48 in which 30 the prepolymer solution and catalyst solution were combined by the same means in a ratio of of 3.4:1 by volume (prepolymer solution:catalyst solution).

Mixing of the combined stream prior to injection into *Trade Mark -35- the mold was performed by means of an in-line 6 Inch by one-quarter inch Kenics static mixer. The mold was filled with the mixture and the resulting solid nylon block polymer was removed from the mold at about 2 5 minutes after the start of injection. The polymerization of the prepolymer and caprolactam was essentially quantitative in the formation of the nylon block polymer. Specimens were cut for testing. -36- Χ> >Η W 4J >» —« K? νο ι—< U m CM CM η <9 <9 • • • • U ι-1 ο Ο Ο ο (0 Ο υ Σ C * ο «~ν ·*Ί W 4J ε 3 σ γΗ • ο ε α cn «3 φ JJ 4J Ώ U υ W ω φ (0 cn ο σι σι j ε Μ ο Η ο σ σ» & > Ο CM Η «Ή Η C Σ Η U •μ < Ο α X α κ U ω 0) ϋ V Σ 0« C Μ —, CC Φ «I σ ε ό 1 U σ φ <α ·—* > ω χ: ο υ 0) £ ω ε ο ιη ΚΩ VO φ α W > ΙΟ ισ ΚΩ ΚΩ Vj 03 Χί Η < • ί Ο 9} J α Φ ο φ * ε U < ο* * 10 Γ"( U ε 4) Ε φ ιη 5. ι-Ι CM Η QJ Ο ε Γ C0 Cfi Ο <ν α φ Η ιΗ Η CM Ό φ X Φ U ω σ α U <0 SZ υ φ XI Η σ α! 3 6 C0 σι Ο Η ο <9 ** rr ιη m £ X < ω m « 37 5 10 15 20 The nylon block polymers prepared either by hand casting or reaction injection molding in Examples 29-51 were tested for various properties substantially in accordance with the following procedures: Tensile Strength : ASTM D1708 [units are pounds per square inch (psi) or megapascals (MPa)]. Tear Strength -: ASTM D1004 [units are pounds-force per linear inch (pli) or newtons per meter (N/m) ]. Flexural Modulus : ASTM D790 [units are pounds per square inch (psi) or megapascals (MPa)].

Notched Izod Impact . ' : ASTM D256 [units are foot-pounds per inch notch (ft.lbs./in.) or joules per meter (J/m)]. Test results for Examples 29-51 are provided in Table F. Tensile elongation (to break) determined in accordance with ASTM D 1708 for these nylon block polymers was generally greater than 50% and in some cases greater than 200%. -38- ~ — Λ P-S CM ___ >-Ν P»S £ ο Η ΓΟ CM ιΛ ΙΟ 1C CM Ο σ\ CM cn \ m Μ· ο Ο Γ» ο η» σι 1C ο C-* <η 1C 1C 1C ιη «τ «*Η Η Η ΙΛ 1C <Ν pH -Η ~ >-ρ* W •«•p 'p \ Ό Ο Ν Ο <Μ η* ΟΙ ο\ <η σι cn in ο ΙΛ CM tu ω m < Μ ε ι ·° Η Η pH pH pH pH u Μ 1 ΓΗ 0) ·% XI X) *p| »χι UH P-. . P*S P\ PS to ,ΡΉ σι Η O pH cn vc cn CO *T CM in CM w <σ Γ- η h m o r- e cn CM CO m VO «5 CU η m in pH in CM cn m r*· M· vo CM pH £ Η Η pH pH pH pH CM pH pH pH pH pH O' »—· »—» —* «aP sp •-P w «—» **p ΓΗ ί Ό (0 0] m ' ΡΡ» Λ ___ __ _ 5 τ: β Γ* CO ic cn in n> m M* M* m m 00 Ο .d 0U *0 0> Xl £ 1*4 o cm m pH pH 1/) VC ro pH vo σι ϋ >4 τΗ ΓΓ «-ρ Μ* *3· n* —* »—· *-p *—» >*P ’-p v-* S—' S—» —· O Μ σ UH d Vi Ο o o o o O O o o o o o c r- o 04 ιο m VC VC VC VO CO VC vc VC vo m u Ο Ο ν 0) 0) to αι pH ε c ε Cl « 0) >. ε Ol o pH CM m M· m vc r·* co σι o pH ? pH ns CM n m m m m cn cn m cn cn n· O o o X 0* Ol CO * ο Μ 39 —V N* ___ CN ε H r* r* © VO p·* VO © \ "C CN rH VO ΤΓ VO r* o CO 3 VO <7 H *H VO © © © **"* c JJ M Ό ϋ V O © o O r-1 eo m © © Ο ¢1 Ν β. 01 «Ν CO CN on CN rH CD © p** t—1 e JQ «Η CN *H rH jH Μ rH X) lU . <—* © m — CN r- m pn fO <0 to o O r* CN m © © © Qj n· m o m CN •N· CO H rH Σ ·—< <—< N* H *H «Η CO H rH rH 01 u 3 m 3 Η l X 3 o m © © CO CO rH © n O c 0) Ό «—< H CO in CN rH CN pv © o r-J Θ X cn rH CN *-H CN H H *1— ίΐ4 £ •H M (Q c Oi • CU > a >r" * •M c a> m V) l · *—r x-> -** —» •—. —* .—, __v o © o a O O O © o o OJ jj a r* VO CN On ro in "Ό £-* CO s CD rH CN CN in © in © p^. C oj VO VO m VO VO © VO vo © «Ο © 'O* 1/) 03 III Q_ 0) E a * * 5 fO X N I rH CN m N* in VO r- © © H LU rH O <0 X rr N* N* «3» «3* 3· *3* N* in © * o. «1 in o 40 EXAMPLES 52-117 Examples 52-117 demonstrate the unexpected results exhibited by nylon block copolymers prepared from acid halide functional or acyllactam functional 5 material containing either polyether segments having minimum molecular weights of about 2,000 or polyester segments containing polyether segments having minimum molecular weights- of about 2,000.

A. Preparation-Acyllactam Functional Materials 10 Acid halide functional materials were · prepared from the polyethers listed below in Table G. The preparation of these acid halide functional materials involved preparing solutions of the desired polyether and terephthaloyl chloride in 15 tetrahydrofuran. A sufficient quantity of an acid scavenger, triethylamine, was added to each solution, so as to precipitate -out of the solutions white amine hydrochloride. The molar quantities of the particular polyether (PE) and terephthaloyl chloride (TERE) used 20 for each solution are shown in Table H.

For each particular polyether different acid halide functional materials were prepared. In each case, acid halide functional materials containing polyether segments and acid halide functional 25 materials containing polyester segments (comprising the polyether segment) were prepared. These polyester segments were formed by the linkage of polyether segments with terephthaloyl chloride residues. Acid halide functional materials containing polyether 30 segments were prepared from mole ratios of 2:1 for diol derivatives and 3:1 for triol derivatives, while those materials containing polyester segments were prepared from mole ratios of 4:3 for diol derivatives -41- and 5:2 for triol derivatives. These acid halide to polyether mole ratios are listed in the following tables under the heading AH/PE.

Batches of acyllactam functional materials 5 were formed by adding to each solution of acid halide functional material a solution of caprolactam and triethylamine (an acid scavenger) in tetrahydrofuran. The molar .quantity of caprolactam used for each batch is shown below in Table H.

The addition of the caprolactam solution to the solution of acid halide functional material was accomplished over a period of about 7 minutes. Each solution was heated to reflux at 76°C and maintained as such for about 1 hour. The solutions were then 15 allowed to cool and about 100 ml. of tetrahydrofuran was added to each. Each batch was then filtered and washed with more tetrahydrofuran (about 2 washings of 75 ml.). The remaining tetrahydrofuran was then removed under vacuum at 80°C over a period of about 3 20 hours.

The IR spectrum of Batch 1 showed no hydroxyl absorption but a strong ester carbonyl absorption with a weaker amide carbonyl absorption. This confirmed the preparation of the acyllactam 25 functional material.

TABLE G Polyethers Designation Description Pluracol P1010 (P1010) - poly(oxypropylene) diol 5 Voranol 2010 (2010) PPG 3025 (PPG3025) 10 PPG 4025 (PPG4025) Thanol SF 395.0 (SF3950) 15 Voranol CP2070 (CP2070) 20 Voranol CP1500 (CP1500) Pluracol GP3030 (GP) •liax 11-34 (NIAX) 25 Thanol SF6503 (SF6503) 30 Pluracol. P-380 (P380) (Molec. wt. about 1,000) - poly(oxypropylene) diol (Molec. wt. about 2,000) - poly(oxypropylene) diol (Molec. wt. about 3,000) - poly(oxypropylene) diol (Molec. wt. about 4,000) - ethylene oxide capped poly(oxypropylene) diol (Molec. wt. about 3,500 with the functionality of the composition being about 2.1) - poly(oxypropylene) triol (Molec. wt. about 725) - poly(oxypropylene) triol (Molec. wt. about 1,500) - poly(oxypropylene) triol (Molec. wt. about 3,000) - ethylene oxide capped poly(oxypropylene) triol (Molec, wt. about 4,800) - ethylene oxide capped poly(oxypropylene) triol (Molec. wt. about 6,200) - ethylene oxide capped poly(oxypropylene) triol (Molec. wt. about 6,760) -43- e ' » «·—, *-* <>. «·>% in J««V o (a n Is- *3· Γ- · A A (A © O' CM in CM 09 o © m CM © © O © a a a) ro CM O 1 iH O CU ca cu H cn H ro *H ro H O o n n ro CM pH pH H CM OU 0« Cu o* CU a o CU > a. cu Ώ u o u & £ o jj a H CM co *0* in © r* CO cjv o fH CM CO ^3· © <0 z PM rH pH pH rH Ή £Q © in 44 E Λ3 * r-% <·"»· •I’—· JJ ** <«» λ CO υ to ΓΟ m (H CM CM CM CM Ή 0) o cn ID ID SO CD r"t cn n * *—». t*s (0 m m *—H ω 0) r- m *c* c* O «3· o cd a; rH ΓΟ m » U to o σι #—» Cl . < ID 00 m H w b m O Z CO CL o> λ υ ·· jj o ID r- © σ\ o H CM on ra z H H H CM CM CM CM CO m 45- B. Preparation of Nylon Block Copolymers Nylon block copolymers were prepared by reacting each batch of acyllactam functional material with caprolactam in the presence of catalyst, caprolactam magnesium bromide. The method used for combining these materials was a reaction injection molding. This technique is well known in the art and involves directing a stream of acyllactam functional materials dissolved in caprolactam and a stream of the caprolactam magnesium bromide catalyst dissolved in caprolactam into a heated mold.

A catalyst solution was prepared for use for in preparing each nylon block copolymer example, except Examples 84 and 87, by charging a 3,000 ml. flask, which was equipped with a stirrer, thermocouple-controlled heater and nitrogen inlet and a distillation head, with 1,650 grams of caprolactam. The caprolactam was dried by distilling off 50 grams from the flask under a vacuum (using an oil pump to provide a vacuum under 1 mm.) at a pot temperature of 125-130°C. The vacuum was released to a nitrogen atmosphere and the flask with the caprolactam cooled down to 75°C. All atmospheric pressure operations were performed under nitrogen. Once the caprolactam was dried, 120 ml. of a 3 molar solution of ethyl magnesium bromide in diethyl ether was added over a 10 minute period while maintaining vigorous agitation.

The solution temperature was maintained at 100°C. The evolved ethane and ether were removed by degassing under a vacuum (less than 1 mm.) for an hour at 90°C. The catalyst solution was maintained, at 90°C. and 200 ml. portions were drawn off for use to prepare each sample. The prepared catalyst solution had a molarity of .225.

Prepolymer solutions were prepared, except for Examples 84 and 87, by dissolving a prepolymer, which was an acyllactam functional material prepared in accordance with earlier Batches 1-23, in caprolactam. To each sample solution 0.5 grams of Flectol H antioxidant was added. The prepolymer solutions were dried by distilling off 25 ml. of caprolactam. The sample solutions were cooled to 85°C.

In Example No. 84, the catalyst solution was prepared according to the procedure described but using only 225 grams of caprolactam which was dried by distilling off 25 grams. Nineteen (19) ml. of a 3 molar solution grams of ethyl magnesium bromide was added to the caprolactam according to the procedure described, above. The catalyst solution was then maintained at 90°C.

The acyllactam functional material f°r Example 84 was not dissolved in caprolactam. Instead, 181 grams of acyllactam functional material was injection molded so as to obtain a 30% by weight of polyether in the final nylon block copolymer. 1.5 grams of Flectol H antioxidant was added to the acyllactam functional material prior to injection molding.

In Example No. 87, the catalyst was prepared in the same manner and quantities as described above for Example 84 with the exception that 16 ml. of a 3 molar solution of ethyl magnesium bromide was used. > Again the acyllactam solution was not dissolved in caprolactam but 159 grams of the acyllactam functional material of Batch No. 12 was used.

The specific prepolymer batch number and the amount of prepolymer and caprolactam employed in preparing the prepolymer solutions for each of Examples 52-117 is shown in Table J. * ΰί g σ» ε <α ο V- α «π CJ ν • αι ο ε z »*3 >1 fH JS ω 0 υ a jj m o >0 < ν CD ε* α- u ο O CO £ 2 u « «—4 >t «3 O r-4 C M Q H 0« &4 OJ m CO tn 03 *—< «Τ CO o r—f 03 •q· cn a Ό » Ο Ν 1Λ Οη to ο m r* ooooooooooooo {ΝηΗΝΜΗΝΛΗΝηΗΝ dP c l* rH a O <0 a o u a* ,—. in 0) ε σ σ u (0 u .e Φ o s- > 4J rH c O 3 a O 0) ε V< c Ο.

U -, 1 rH .c O o a a <0 u 03 Cu 03 •C 2 oiOr'-f'Jcotnfo.-scrvMr^cnm ·-* —* Ή «Η «Η*-ί (H r-t ,-j in o in -50- 4J C 0 o a < 6h c ο xi 3 t—4 Ο VI u 0) E > r-i Q a a u Cu o 03 m a\ CM CO m -3· «Τ n CO r- r-i in cm i£3 CO CO M· ro σ\ m CO H iH H iH r-i H a rl H CO VO ov CO ί o rH »H CM 00 VO CM CO in o in ο) CO *3· CO CM CO #H H r-i H rH iH u v a> as £ Z aj a) >* «3 rH C O CU tw ooooooooooaoooo ΝΓΟΗΝΟΗΜΠΗίΝΡΙΗΝΠΗ a E «3 X « O ^ CO 00 cNro V4 r-4 a Ο «j α 0) u Cu «*-. OJ Φ ε CP σ U *—» «J u Λ Ο S ' > JJ i—l C G 3 a Ο 0) ε U < cw Ut , ο o ε z > Γ"« .c ο u α J-» V fa U CQ CL Ό - Ι-ι o 4J αι □3 C x Z 0 4J . υ 0J r-4 >ι <0 >"5 r—1 c c -f ω α Cu α t** *c < · j Ε-* m in νο νο νο ρ» p* ιΗ »Η r-4 *—4 Ή r-4 »Η Ο Ο Ο Ο Ο Ν η Η Ν Π o CO G\ •q* CO H to CN 04 03 m P-t CO «Τ o \o n o to o P- O p- «3* o H r-4 #-4 H H H H CO VO #-4 p- «3* σ\ co CO r- o ΤΓ p* H r4 r-4 cO O' o H ro VO o H rO VO o r-4 CO VO O H οοοσοοοο NfnHNMHWm a tn vo p- CO as o r-4 Pi CO in VO C" © i e1 σν cr. φ σ» c\ o O O a o o © © © <0 H H i—l H H H H r-4 Μ ΙΠ Ο γ—I 52 Ό •Daου caa« * C 4-W 0 0) ηΗ £ cn 3 —»· ι~Η e Ο <0 W .W CJ CM O CM 03 in W <0 H O c- β) H H H H »H £ o L Η a Ο «j 0J a φ Li . CL n Φ 6 ςρΙ cr u "W «3 V4 J3 Φ Ο £ cn \n CO cn P- o JJ H iH jC © o σ iH cn ro O υ CM CM CM CM CM CM a φ a £0 a Ο 00 Η Γ"* «Η α φ u \η θ'c Ιή h Ήκο σ> >» U Ό C Ό Φ> Ο £ CM (Μ Φ Ν Ν W Φ <05 * u υ Φ CO JZ z JJ Φ rH 5s n H c O •*4 04 Cu ** C ΛΗ α 6 ιΰχ ω Ό Φcn u Φ Λο uC 3 Οε ΙΤ) -53· The nylon block copolymers in Examples 52-83, 86, and 88-117 were prepared by pumping the prepolymer solutions and the catalyst solution in a 1:1 stream volume ratio into a closed mold heated to 140°C. having an internal cavity of 20.32 cm. x 20.32 cm. x 3.175 cm. Examples 84 and 87 were prepared by pumping the prepolymer and catalyst solution in a 1.52:1 and 1.13:1 stream volume ratio, respectively, into a similar mold. Mixing of the combined streams prior to injection into the mold was performed by means of an in-line 4 inch to one-quarter inch Kenics static mixer.. Examples 52-117 were then tested to determine their impact and flexibility properties substantially in accordance with the following procedures: Flexural Modulus, Notched Izod Impact (which were described above) and Driven Dart: Procedure described in November 1974 SPE Retec Bulletin by V. A. Matonis -15.88 mm.(5/8 in.) diameter Dart driven at 111.76 ra./min. (4400 in./min.) impacted against a 3.2 mm. (1/8 in, by 50.8 mm. (2 in.) diameter disc of the specific NBC which was held against a 31.75 mm. (1 1/4 in.) sample ring at a temperature -29°C. (-20°f.). Energy measurements made with a Nicolet 1094 Digital Oscilliscope [units are joules (j) or inches per pounds (in.-lbs.)) -54- The test results are provided in Tables (K-l) - (K-4) below. The examples are arranged according to polyether type (either diol or triol derivatives), percent by weight of polyether in the nylon block copolymer, and by the AH/PE ratio to highlight the effect of molecular weight upon impact properties.

I « ω Ω m < c 0) > •τΗ u Ω Ό O N <0 u 3 X (D rU Cu *·<* «-Η «•H. ID Γ* σ\ o ·* • • « tt CM 00 r- in JQ H P* M U \ U -« <0 C Q ·*·« cn H σι m • « o CM o 00 C . «s ^k. «9· CM m m \ • « .· BS o *—1 rt i-H CM -Q w O W u r-l 0) •rl U O i > XI 0) 03 > s •h & H w «3* a\ iH cn \ ui X 0 CM ID ID σι cn n V X CU H a < • dP <-s H o * o ·* H m «-* CM l Q ««H «—» j—x o σι o ID Γ» σι w rM cM CM CO m ID r cn CM CM cn CM 3 X H 3 -r« Ό O a £ >— as r* CM CM in «5 ID H r- ID m CU CM in σι «3* 00 £ CM H iH CM H 0P' <3 CM U) •«9· cm ID *D r-H • · m cn CM CM H f**» 03 ID Ρ» • • • • « o CM iH CM cn cn cn in in r- « • • • • o CM CM in m s·^ v»» H in in co m «9» »H σι m cm n m o in cm i-i m p- r-< co Ή i-| CM i-l w a\ CM CM σι 00 ID r* CO p* 1? Q T? σι CM in (8 1) © CM • • • • • o © © © O *—' Γ- r> o P* H *3· H © © (O H CO • • • • • · V Γ*·. CO CM CM H ιΛ CO ON IN CM • • • • • © © © r* r-i W (H u *-· V s, xi 9) > • r< VO in CM CO 'd O H r- © a> © 0« tj· in co m -U c 0 © V ΓΟ r4 1 in p- ON © ON X © \o Γ' ·*—» H ··—» '»* *«* W m < O O m m n-t CM in TP ro CM © << in H *? O 10 N CO in © P- Γ- m 57 __ CN in *· • • • 01 »—{ m 10 η •ο-* *—* CM c rH u ·* •Pi «—* •w· xj rH 0) ο Ό ϋ 1 > •Η U O <α * •«4 AJ φ N α XI JJ <0 J0 M ε ΙΜ 10 α: XI w > φ ε **Η 01 > 10 in o \ α· rt Η r* 03 η φ X 0 Q S & -1 dP m Ο ι-Η σ I Η «* *-Η ο W Π .__„ η &« iH ^3* H Η H r~ <0 01 X cn cn CM W 3 Η * 3 Φ Ό 01 H Ο α fe £ ·*-· m M* ox (0 ιο CO π* rt H pH pH pH pH rH t-4 *T n cm m o\ pH σ 10 ΙΛ pH cn CM Ox < CQ ro οι (Λ ph cn m 00 CO ON O Q rH pH •58· η η α\ νο η σ· σΝ Ν d Η in cn m • • • • Ο ο CM id vo CM CM CM CM -Η CO in VO Ov • • • • • m CM H o *-4 rH H 4) JZ α>> ϋΐ Ο Ρ* (Λ Ν Φ η νο Η ΟΗ VO νο νο ΙΛ 4J C ο V CM Ia: m μ3 ¢0 ο ον ο μΟ m νο · ^ w W Ο —* νο ί"4 Ρ-νο ιη m H m o •H rl ςη ο σ ή 59 w jQ \ Ο Η ¢1 rt Η Η Π Η \β \[) Ν «1 «η 03 «3 w w Ή w <Ν σν σ\ ja W O XJ r-1 0 •*4 ό o r > X) a 0 «3 · M <0 JC N Q, JJ AJ a AJ μ ε uj (0 0 n -- > ω > £ Qj m U \ O ϊ o <ΰ 33 & a < - dP ω H cn o — o • «-Μ m m < 1 Q e- O I co •O· ON on VO VO 1 * • • • • • H CN in VO ON o\ M CM H VO CM ON o O O PO • • • « • • » • H o r4 H CM CO CM *— X—» w· H U H o ΤΓ O o VO Ή in r4 H *—< CN VO (Π 0) u a 3 rl X 3 VO vo CM H CD CO CO o o· r* CN CO CO iH CM rH H CM rH w w r* η σι Η Η Γ» U1 (Μ > (Μ CVJ Ο Ο Ο CN CM Ιίΐ Η Ρ*» Ρ3 οι ΙΛ VO VO Γ*>* Γ*» VD CN C0ιη νο νο •60 «Mu CN o © r- 04 • • • * • GO r* o in 0- o H m οι 04 m ·"-* m rH O in • • • • • CM m ID VD* 04 n ro vo p*· VO H • • • • CS N r> 04 CO w» H rH 0) £ XJ a) >· CO m rH σ» 04 t Ι-» (S m CO ro Ό O rH VD r· *H fl- JJ G c*> 0 O O fn «Μ» fO σ» 04 in ID rH | o o in ID VD ^•4 H rH "τ' W ca < CM tn σι m H m o ID in 04 j> ,r- o «Τ r—f r- m σι m H m VO ID r·» CO in 61 if··» .*-» .·>» rt o 00 cn VO m cn o\ CM Cl ^ ·· • • Λ • « · UJ CM *0» tn CO in in o VO r- σι cn jQ ·—* CM cn CM σι cn N_p« © o *3* vo fH *—* »-* cn *3* CM c \ V» «·>* w 4) XJ .· > u c ♦Η ffi •H U Ω w O fH m •3 M· f- o fH VO © o o © CM rH cn • • • • • • - « • • • • · — CM CM m © o M1 © oi fH fH cn m cm C ___ _ «-» —H •H tfl σι CO CO VO M· CM CO cn r* O © X • • • • • · m O H fH fH *3* CM O *r rp cn .fl -** '•Τ’ Ί—» VH tH fH iH rH w •»-f «*—» » XJ » e> O U Ό O ·· > •H u V Q (Π Jrf •H * AJ 03 j= S a (M AJ .C X) w ε »—» «I cz AJ σ M ε 03 ω H VO VO VO CO > fH © © «Η f* Γ- t X fH ω > O σι Ol ^3· CM iH »H in n —» ,—k 0-» .»">% A *—>» ,—v /»«* o u in CM CO CM H VO n CM © © VO •h in H fH t- O m CM σι •Φ 62· JJ c 0 u ia CQ < pH o 0« o*> o O in o * • • • » o in H .H lO p* V O crv Cl rH pH CN ro ««-* ___ 00 r- σι N 10 r- m CO in in © o CN ^a· m © in r* η As indicated in Table (K-l) - (K-4), the impact property test results, i.e. Izod Impact and Driven Dart, of nylon block copolymers containing polyether segments or polyester segments having 5 polyether segments exhibit unexpected results when the polyether segments have a minimum molecular weight of about 2,000. Below this preferred value of 2000 are the Examples 52-57 and 82-87 which contained polyether segments with molecular weights of 1,000 and 725, respectively, and which 10 generally exhibited significantly lower impact properties than the reamining examples wherein the molecular weights were at about 2,000 or more.

Furthermore, as indicated in Table K, the impact property test results of nylon block copolymers 25 containing polyether segments and polyester segments having polyether segments, exhibit unexpected results when the polyethers were derived from triols as compared diols, see Examples 94-96 and 97-99 for triol derivatives and Examples 64-66 and 67-69 for diol 30 derivatives. Both the triols and diols utilized had molecular weights of about 3,000.

Also as stated above, a minimum amount of cross-linking in the composition results in better -64- properties. This is seen by comparing the impact properties of those nylon block copolymers prepared from PPG 4025 (Examples 70-72 and 73-75) with those prepared from Thanol SF 3950 (Examples 76-78 and 5 79-81) . Thanol SF 3950 w'as a composition having a functionality of about 2.1, thus allowing for some minimal cross-linking.

Examples. 11,8-122 . Examples 118-122 were prepared to 10 demonstrate the effect of specific R groups had upon impact and other properties of nylon block copolymers made from prepolymers containing such R groups hereinabove described (see Formula I).

As discussed above, preferred R groups are 15 hydrocarbon groups and hydrocarbon groups having ether linkages which provide at least three successively bonded elementary atoms between any two carbonyl groups bonded to R. Acyllactam functional materials were made by reacting a polyether (NIAX) with various 20 acid halides, as specified in Table L below. Some of the acid halides used (i.e. O-phthalic acid chloride and fumaric acid chloride) formed R groups that provided less than 3 successively bonded atoms between the two carbonyl groups. The remaining halides 25 forming R groups others providing 3 or more successively bonded atoms between 2 carbonyl groups. The resulting acid halide functional materials were then reacted with caprolactam (the specific process of preparing these materials is similar to the process 30 described hereinabove and will not be discussed in detail herein) to form acyyllactam functional materials. These acyllactam functional materials were blended into caprolactam and then reacted with a -65- catalyst-caprolactam solution (prepared according to a process similar to the process described above) to form nylon block copolymers having 20 weight percent polyether content. The resulting nylon block 5 copolymers were subjected to the following tests: Driven Dart (described above) and Acetone Extractables: Percent weight loss after 24 hours in a Socklet Extractor. -66- 08-21-1223 φ Η Δ φ <0 *** SO CO rH c 4J l£> P* ro p* o ο υ • • • • • χ> <0 c*e rH rH m rH H rH m rH 0) XI H *a* ·—· W > 4-> rH m H 01 ω Φ Ό Ό Ό »rl •r4 •H U W Li Φ

Claims (26)

1. 2. A composition of Claim 1, wherein said acid halide functional materials consist of those of the formula 0. r 1' Z[-0-C-R(C - Xa]b

2. 3. A composition of either Claim 1 or Claim 2, wherein R provides at least three successively bonded elementary atoms between any two carbonyl groups bonded to R.

3. 4. A composition of either Claim 1 or Claim 2, wherein R is meta-phenylene or para-phenylene.

4. 5. A composition of either Claim 1 or Claim 2, wherein R is derived from an acid halide selected from adipoyl chloride, sebacic acid chloride and azelaic acid chloride.

5. 6. A composition of any of Claims 1 to 5, wherein Z is a segment of (1) a polyether having a minimum molecular weight of about 2,000; or (2) a polyester containing polyether segments, the polyether segments having a minimum molecular weight of about 2,000.

6. 7. A composition of any of Claims 1 to 6, wherein Z is a segment of: (1) a polyether derived from a triol; or (2) a polyester containing polyether segments, the polyether segments being derived from a triol.

7. 8. A composition of Claim 7, wherein the polyether in (1) or polyether segments in (2) have a minimum molecular weight of about 3,000.

8. 9. A composition of any of Claims 1 to 8, wherein Z comprises segments of poly(oxyethylene), of poly(oxybutylene), of poly(oxypropylene), or of a block copolymer of poly(oxypropylene) and poly(oxyethylene).

9. 10. A composition of any of the preceding claims, wherein X is chlorine.

10. 11. A composition of any of Claims 1 to 9, wherein X is bromine.

11. 12. A process for the production of a composition according to Claim 1, that comprises reacting a polyhydroxyl material Z-(OH)χ, wherein x is an integer equal to 2 or more with the average value of x for all the said polyhydroxyl materials being greater than 2, and Z is (1) a polyether; (2) a polyester containing polyether or polymeric hydrocarbon segments; (3) a hydrocarbon; (4) polysiloxane; or (5) mixtures thereof; with an oxalyl halide or an acid halide material containing at least two carboxylic acid halide groups. 0 wherein y is an integer greater than 1, generally 2,3 or 4, preferably 2 and R is a di- or poly-valent group selected from hydrocarbon groups containing either linkages, to produce acid halide funtional materials.

12. 13. A process of Claim 12, wherein said acid halide funtional materials consist of those of the formula; 0 0 wherein Z,R,X, a and b are as defined in claim 1.

13. 14. A process of either Claim 12 or Claim 13, wherein R provides at least three successively bonded elementary atoms between any two carbonyl groups bonded to R.

14. 15. A process of either Claim 12 or Claim 13, wherein R is meta-phenylene or para-phenylene.

15. 16. A process of any of Claims 12 to 15, wherein the acid halide is selected from adipoyl chloride, terephthaloyl chloride, isophthaloyl chloride, sebacic acid chloride and azelaic acid chloride.

16. 17. A process of any of Claims 12 or 16, wherein Z is a segment of (1) a polyether having a minimum molecular weight of about 2,000; or (2) a polyester containing polyether segments, the polyether segments -71- having a minimum molecular weight of about 2,000.

17. 18. A process of any of Claims 12 to 16, wherein Z is a segment of: (1) a polyether serived from a triol; or (2) a polyester containing polyether segments, the polyether segments being derived from a triol.

18. 19. A process of Claim 18, wherein the polyether in (1) or polyether segments in (2) have a minimum molecular weight of about 3,000.

19. 20. A process of any of Claims 12 to 16, wherein Z is a segment of: (1) a polyether serived from a tetrol; or (2) a polyester containing polyether segments, the polyether segments being derived from a tetrol.

20. 21. A process of Claim 20, wherein the polyether in (1) or polyether segments in (2) have a minimum molecular weight of about 4,000.

21. 22. A process of any of Claims 12 to 21, wherein Z comprises segments of poly(oxyethylene), or poly(oxbutylene), of poly(oxypropylene) or of a block copolymer of poly(oxypropylene) and poly(oxyethylene).

22. 23. A process of any of Claims 12 to 22, wherein X is chlorine.

23. 24. A process of any of Claims 12 to 22, wherein X is bromine.

24. 25. A process for the production of a composition as defined in Claim 1 substantially as described herein with reference to the Examples.

25. 26. A composition as defined in Claim 1 whenever prepared by a process as claimed in any of claims 12 to 25. Dated this the 29th day of December, 1989. BY: TOMKINS & CO., (Signed) (Γί0^A lhantc' Agents,

26. 5, Dartmouth Road, DUBLIN 6. -72-