CN1022040C - Shock-resisting composition containing modified block copolymers - Google Patents

Abstract

Thermally stable modified selectively hydrogenated high 1,2-content block copolymer wherein a functional group is grafted to the block copolymer in the monoalkenyl-arene block and impact resistant polymeric compositions comprising: (a) 3-50% by weight of such modified block copolymers, and (b) 50-97% by weight of polyamide having a number average molecular weight of at least 5,000 or a thermoplastic polyester.

Description

Shock-resisting composition containing modified block copolymers

The present invention relates to a kind of Formula B n(AB that uses) segmented copolymer functionalization, selective hydrogenation represented of oAp, n is 0 or is at least 1 integer in the formula, o is an integer, be at least 1, p is 0 or is at least 1 integer, A mainly is a poly-mono-alkenyl-aromatic hydrocarbons block, and B mainly is a poly-conjugated-diolefin block before hydrogenation.

The present invention also relates to impact-resistant polymer composition and the method for preparing functionalization, selective hydrogenation segmented copolymer.

Known segmented copolymer can carry out anionic copolymerization with organic alkali metal as initiator and obtains with conjugated diene compound and aromatic vinyl compound.The characteristic of this based block copolymer is different, and it depends on the content of aromatic vinyl compound.

Aromatic vinyl compound content after a little while, the segmented copolymer of gained is a kind of so-called thermoplastic elastomer.This is a kind of very useful polymkeric substance, and when it was in not sulfided state, it had the elasticity of rubber, can obtain various application, as does at the bottom of the cemented shoe, the impact property properties-correcting agent of polystyrene resin, tackiness agent, tackiness agent.

The resin that segmented copolymer generated of aromatic vinyl compound content height [for example 70%(weight) more than] has impact strength and transparency preferably, is widely used in packing.People once proposed many suggestions to the method for preparing this based block copolymer, as US Patent specification 3,639,517.

Why some aromatic vinyl polymer has elastomer performance, and part is because their degree of branching.Though the basic main chain of aromatic vinyl polymer is the carbochain straight chain, those aromatic vinyl polymers with elastomer performance always have pendent alkyl groups.For example, ethylene-propylene rubber(EPR) (EPR) just has the structure of methyl side groups, and these pending methyl groups make it have elasticity and other elastomer performance just.If what generate is unbranched straight-chain polymer (as certain polyethylene) basically, it is elastomeric that the polymkeric substance that is generated is gone up right and wrong substantially so, or in other words, be quite firm, it belongs to the typical heat thermoplastic plastic, does not have like rubber rebound resilience or high elongation, and tensile strength, the tension set of no yield-point is very little does not possess desired elastomeric other characteristic.

Segmented copolymer is existing to be produced, can consult US Patent specification Re 27,145, this based block copolymer comprises that mainly those have the multipolymer of A-B-A structure, two end polymer block A comprise vinyl-arene thermoplastic polymer block (as polystyrene) in the formula, and B block then is to select the conjugated diolefin polymer block of hydrogenation.The ratio of thermoplastic end-blocks and intermediary elastomer polymer block and the relative molecular weight of each block are kept in balance, and could obtain to have optimum performance bonded rubber, and in fact it is only does not so need to vulcanize the rubber that just has curability.And these segmented copolymers not only can be designed to have the polymkeric substance of this significant advantage, and can also use the thermoplastic plastics shaping apparatus processing, and can be dissolved in various more cheap solvents.

Though these segmented copolymers have a lot of outstanding technological merits, one of limitation that it is main is their susceptibility to oxidation.This is because their unsaturated characteristic causes, but this unsaturated characteristic can especially be reduced to a minimum by the hydrogenation at the middle portion that contains the polydiene block by the hydrogenation of multipolymer.Hydrogenation can carry out like that selectively as US Patent specification Re 27,145 is disclosed.These polymkeric substance are segmented copolymers of hydrogenation, this multipolymer has the A-B-A configuration before hydrogenation, wherein each A is the aromatic polymer block that an alkenyl replaces, B is a butadiene polymer block, it is 1 that the condensation diene units of 35～55 moles of % is arranged in the butadiene polymer block, the 2-configuration.

These select the ABA segmented copolymer of hydrogenation, because it has the hydro carbons characteristic, when being applied to the shortcoming that just seems when those need have the occasion of adhesive power to polar surfaces.This class example comprises the toughness reinforcing and consistency of polar polymer (as thermoplastic engineering plastic) and based on tackiness agent, sealing material and the coating of hydrogenation elastomer block copolymer and the adhesion of high energy substrate, and the hydrogenation elastomerics is used to strengthen polymeric system.But with the official can unite to be incorporated into just can produce on the segmented copolymer hydrocarbon polymer the interaction that can not have, thereby solved sticking problem and enlarged the range of application of this material.

Except greatly improving the interface adhesive power in the polymers copolymers, the styrene-ethylene/butylene-styrene of functionalization (S-EB-S) component also makes polymeric system have frequent needed outside adhesion characteristics.These characteristics comprise: to the adhesive power of the toughener (fiber and filler) of polymeric system; Based on tackiness agent, sealing material and the coating of the S-EB-S polymkeric substance of functionalization adhesive power to substrate; Based on the system of S-EB-S polymkeric substance to decorating the adhesive power of (as printing ink, paint, priming paint and metal); Participate in chemical reaction, as make protein (as heparin) have consistency with blood; Tensio-active agent in polar-nonpolar water dispersion or nonaqueous dispersion.

The S-EB-S polymkeric substance of functionalization we can say it is the S-EB-S polymkeric substance of industrial production basically, and it is by there being the chemically combined with it S-B-S hydrogenation of polymer of functional group to make on its styrene block or the ethene-butylene blocks.

People have done many trials, want to improve adhesivity, green strength and other performance by the functionalization of segmented copolymer, and have proposed the polymkeric substance that several different methods is come synthesis of conjugate elastoprene functionalization.

US Patent specification 4,292,414 and 4,308,353 described a kind of with maleinization compound grafted, mono-vinyl-aryl/conjugated diene block copolymer that 1,2 content is low.But this method is limited to those reaction conditionss that suppresses free-radical generating with free radical inhibitors or stablizer (as phenol type, inferior phosphorus type or amine stablizer) commonly used.This method only limits to thermal addition reaction or what is called " ENE " reaction.The specific practice of this reaction depends on the reactive site that nonsaturation determined of stock polymer.In order to make stock polymer have favourable functionality or grafting degree, suitable residue degree of unsaturation be arranged.The stock polymer of hydrogenation is can reaction significantly in this currently known methods fully substantially.

US Patent specification 4,427,828 have described a kind of similar modified block copolymer, but 1,2-content height, it also is to make with " ENE " reaction.

The polymer-modified product that " ENE " method described in the prior art is produced, it is on the allylic of this polymer backbone double bonds replacement to have taken place.The reaction of it and maleic anhydride can be expressed as follows:

A. react at the unsaturated double-bond place of main chain

B. react at unsaturated ethylene side group place

Be illustrated among the formula a on two keys of stock polymer addition takes place, two keys that b is illustrated in side chain carry out addition.Substituting group is on the double-stranded allylic carbon atom after addition and the isomerization.

This because its thermostability is bad thermal destruction takes place easily at the substituted polymkeric substance of allylic.Technical known allylic substituting group is known as instead easily-reaction [seeing B.C.Trivedi, maleic anhydride one book (Plenum Press, New York, 1982) the 172-173 page or leaf of B.M.Culbertson] of ENE.

In addition, as previously mentioned, because ENE reaction requires the stock polymer parent to have suitable degree of unsaturation, so the copolymer products of the functionalization of gained will have the residue degree of unsaturation of certain degree, must be easy to oxidation.

Now worked out a kind of method functionalization, that select the segmented copolymer of hydrogenation for preparing, this segmented copolymer has fabulous outward appearance and mechanical property, and Heat stability is good especially can be used for and other polymer blending.Therefore, the present invention just provides a kind of method functionalization, that select the segmented copolymer of hydrogenation for preparing, and this method comprises uses Formula B n(AB) ₀The segmented copolymer of the selection hydrogenation that Ap represents contacts in the presence of the polar compound that is selected from tertiary amine and low molecular weight hydrocarbon ethers with a kind of alkyl lithium compounds (do not comprise and use the tertiary alkyl lithium compound), contain active lithium bond owner chain to generate on the polymer chain, n is 0 or is at least 1 integer in the formula, 0 is an integer, be at least 1, p is 0 or is at least 1 integer, A is mainly a poly-mono alkenyl arene block, B is mainly a poly-conjugated-diolefin block before hydrogenation, but and then make this main polymer chain contact the main polymer chain that has the grafting molecule with generation with at least a electrophilic grafting molecule or electrophilic body, but wherein all the above-mentioned grafting of grafted molecules all are connected in the vinyl-arene block of segmented copolymer substantially.

Six of the present invention preferably have scheme and are:

(1) each block A mainly is that molecular-weight average is 1,000～115,000 poly-mono alkenyl arene block;

(2) molecular-weight average of each poly-conjugated-diolefin block is 20,000～450,000;

(3) block A accounts for 1～95% of multipolymer weight;

(4) degree of unsaturation of B block is lower than 10% of original degree of unsaturation;

(5) degree of unsaturation of block A is higher than 50% of original degree of unsaturation;

(6) the grafting molecule contains one or more functional groups.

Characteristics of the present invention provide a kind of method for preparing heat-staple modified block copolymer, its residue degree of unsaturation is low, appearance characteristics, melt flow and mechanical property (as tensile strength and impact strength) are all fabulous, especially can be used for and other polymer blending.

Grafting or replacement take place in modified block copolymer of the present invention in its vinyl-arene block, shown in following type reaction:

The structure (being determined by the position in the vinyl-arene block of functional group on main polymer chain) of the segmented copolymer that replaces improves the thermostability of segmented copolymer greatly.

Can comprise for the conjugated diolefine of utilizing and the segmented copolymer of vinyl-arene: contain 1, the segmented copolymer of 2-microstructure (suitable content is 7～100%, is preferably 35～50%) before any that have an elastomer performance and those hydrogenation.These segmented copolymers can be the segmented copolymers that contains the different structure of various conjugated diene/vinyl arene ratios [comprise that vinyl-arene is up to 60%(weight)].Therefore, available segmented copolymer is that line style is symmetric or radial symmetry or asymmetric and have the general formula of a using A-B, A-B-A, A-B-A-B, B-A, B-A-B, B-A-B-A, (AB) multipolymer of BA structure, A is vinyl-aromatic polymer block or conjugated diene/vinyl arene tapered copolymer block in the formula, B is the conjugated diolefin polymer block.

The molecular-weight average of block A is preferably 500～60, and 000, the molecular-weight average of B block is preferably 35,000～150, and 000.

Segmented copolymer can be with the preparation of any well-known block polymerization or copolymerization process, comprises that well-known order is added monomer technology, increment adding technique or as US Patent specification 3,251,905; 3,390,207; 3,598,887 and 4,219,627 described coupling technology.As everyone knows, in the segmented copolymer technology, can be by the copolymerization of conjugated diolefine and vinyl aromatic monomer mixture, and utilize the difference of two kinds of monomeric copolymerization reactivity ratios, the tapered copolymer block is attached in the segmented copolymer.Different patent specifications comprises US Patent specification 3,251,905; 3,265,765; 3,639,521 and 4,208,356 have all described the preparation method of the segmented copolymer that contains the tapered copolymer block, for reference here and incorporate in this specification sheets.

The conjugated diolefine that can be used for preparing polymkeric substance and multipolymer is the conjugated diolefine that those each molecules contain 4～8 carbon atoms, comprises 1,3-butadiene, the 2-methyl isophthalic acid, 3-divinyl (isoprene), 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 1,3-hexadiene etc.Also can adopt the mixture of this class conjugated diolefine.A best conjugated diolefine 1,3-butadiene.

Polymer blocks A selects for use the mono alkenyl arene polymer blocks better before hydrogenation, be preferably the vinyl aromatic polymer block, the vinyl-arene that can be used for preparing multipolymer comprises: vinylbenzene, neighbour-vinyl toluene, p-methylstyrene, right-t-butyl styrene, 1,3-dimethyl styrene, alpha-methyl styrene, vinyl naphthalene, vinyl anthracene etc.Best vinyl-arene is a vinylbenzene.Segmented copolymer is styrene-ethylene/butylene-styrene block copolymer preferably.

Should be noted that, if requirement, above-mentioned polymkeric substance and multipolymer are to be easy to prepare with the method that proposes previously, but because these polymkeric substance and multipolymer much can both have been bought on market, usually all would rather adopt the polymkeric substance that on market, to have bought, because the procedure of processing in total preparation process is reduced.These polymkeric substance and multipolymer can be with various known method hydrogenation, are included under the situation that Raney nickel, precious metal (as platinum and palladium) and soluble transition metal catalyzer exist to carry out hydrogenation.The method of hydrotreating that is suitable for is that those make the polymkeric substance that contains diene or multipolymer be dissolved in the inert hydrocarbon diluent (as hexanaphthene) and carry out the method for hydrogenation with the hydrogen effect under the situation that a kind of solubility hydrogenation catalyst exists.These methods are in US Patent specification 3,113, and are open in 986 and 4,226,952, for reference here and incorporate in this specification sheets.When polymkeric substance and multipolymer carried out hydrogenation, make the residue degree of unsaturation in the polymkeric substance of hydrogenation and the polydiene block in the multipolymer was 0.2～20% of the preceding degree of unsaturation of hydrogenation, is preferably 0.5～10%.Preferably B conjugated degree of unsaturation is reduced to below 5% of its original degree of unsaturation.According to another preferred concrete scheme of the present invention, mono-alkenyl-aromatic hydrocarbons unit more than 25% is on average arranged by hydrogenation.The average degree of unsaturation of hydrogenation segmented copolymer has been reduced to below 20% of its original degree of unsaturation.According to another better preferred embodiment, on average less than mono-alkenyl-aromatic hydrocarbons unit of 10% by hydrogenation, and block A preferably accounts for 1～40% of multipolymer weight.

Generally speaking, any material that can react with the stock polymer of lithiumation all is applicable to purpose of the present invention.

For the official can be united to be incorporated in the stock polymer, the reactant that can react with the stock polymer of lithiumation must be arranged.These reactants can be polymerisable or not polymerisable, but preferably adopt not polymerisable or slow polymeric reactant.

Graft reaction comprises the nucleophilic reaction of a kind of lithium alkylide that combines with polymkeric substance or electrophilic body.

The electrophilic body of preferentially selecting for use that can form graftomer in the scope of the invention comprises following various reactant: carbonic acid gas, oxyethane, aldehydes, ketone, carboxylic acid and salt thereof and ester, aryl halide, epoxy compounds, sulphur, boron alkoxide, isocyanic ester, sulfonate (ester) and various silicon compound.

These electrophilic bodies can contain incidental functional group, and for example, at N, amine is exactly subsidiary functional group in N-dimethyl-right-aminobenzaldehyde, and aldehyde is active electrophilic body.Another kind of situation is, the electrophilic body can react and make and himself become the sense position, and for example, carbonic acid gas (electrophilic body) reacts with metallized polymeric and generates carboxylicesters functional group.Can make with these methods and to contain, below one or more functional groups such as carboxylic acid, carboxylate salt and ester, ketone, pure and mild alkoxide, amine, acid amides, mercaptan, the polymkeric substance of grafting sites such as the functional group of boratory silicon atoms.

These functional groups can react with other material that plays modifying function subsequently and form new functional group.For example, the foregoing carboxylic acid of grafted can carry out suitable esterification with the hydroxy-containing compounds of different carbon atom length by carboxyl and obtains suitable modification.In some cases, this reaction can take place simultaneously with graft reaction, but all is to carry out in afterwards the post-modification reaction in most of examples.

The contained grafting part of graftomer is to account for 0.02～20% of total polymer usually, is more preferably 0.1～10%, is preferably 0.2～5%.

Segmented copolymer after the modification still can be used for the Application Areas of the unmodified material of any original employing (stock polymer).Be that they can be used as tackiness agent and sealing material, or with any form easily mix, extruding and mold pressing.

Polymkeric substance can prepare with any method easily.An example that makes functional group combine the method for (mainly being attached in the vinyl-arene block) with stock polymer is a metalation.

It is very easily that the title complex that combines with lithium component (available R ' (Li) x represents) and polarity metallization promotor carries out metalation.Polar compound and lithium component can add respectively, also can carry out pre-mixing before being added to hydrogenated copolymer solution or carry out pre-reaction to generate adducts.With R ' (Li) in the compound that x represents, R ' is generally the saturated hydrocarbyl of any length, but general institute carbon atom quantity is no more than 20, also can be aryl (as phenyl, naphthyl, tolyl, 2-methyl naphthyl etc.), or for saturated cyclic alkyls (for example carbonatoms is 5～7), carbonatoms are that 5～7 the unsaturated cycloalkyl of list, carbonatoms are 1～20 non-conjugated unsaturated aliphatic alkyl, or at carbonatoms the lithium alkylide that one or more aryl are arranged on 1～20 the alkyl.(Li) among the x, X is 1～3 integer at formula R '.Typical example has lithium methide, the sec.-propyl lithium, and the second month in a season-butyllithium, just-and butyllithium, the tert-butyl lithium, just-and the dodecyl lithium, 1,4-two lithium butane, 1,3,5-three lithium pentanes etc.Lithium alkylide must be bigger than the alkalescence of metallization alkyl product.Certainly also can adopt other basic metal or alkaline-earth metal alkyl, but the most handy lithium alkylide, this is because they are easy to buy on market.Equally, metal hydride also can be used as metallization reagent, but the solubleness of hydride in appropriate solvent is little.Therefore, the most handy metal alkyl because their solubleness is bigger, is more convenient for handling.

It generally is very difficult that list makes the multipolymer metallization that contains aromatics and olefmic functionality with lithium compound, and will at high temperature carry out, and this can make copolymer degradation.But as using tertiary diamine and end of the bridge monoamine simultaneously, metalation with regard to carrying out rapidly steadily.It is effectively that some lithium compound uses separately, it should be noted that the lithium methide type.

Surface metalation occurs on the carbon atom that connects aryl, or occurs on the aryl, or occurs on a plurality of such carbon atoms or aryl.No matter be which kind of situation all shows have a large amount of lithium atoms to be connected with intermediary carbon atom (promptly not being the carbon atom of polymer ends) at the different sites of polymer chain respectively, or along the main chain of polymkeric substance, or be connected on the side group of main chain, or both of these case has, but ways of connecting depends on the distribution situation at reactive site or lithiumation position.This makes the lithiumation multipolymer and the sort ofly adopts lithium initiator even multi-lithium initiator makes, terminal activated simple aggregation thing has tangible difference in polymerization process, thereby makes and can all be restricted for the number and the position at the position that connects subsequently.When adopting method for metallising described here, the lithiumation degree depend on the reagent that metallizes consumption and (or) can metallize the base quantity.When adopting the bigger lithium alkylide (as the tert-butyl lithium) of alkalescence, can be without the polarity promotor of metallizing.

Polar compound promotor comprises various tertiary amines, end of the bridge amine, ether and metal alkoxide.

Can be used for all connecting three radical of saturated aliphatic alkyl on each nitrogen-atoms of metallized tertiary amine, the example that belongs to this class tertiary amine has:

(a) chelating tertiary amine, preferably those use general formula (R ²) ₂N-CyHay-N(R ²) ₂The chelating tertiary amine of expression, each R in the formula ²Can be identical or different straight chained alkyl or branched alkyl, this alkyl can be any chain length, and its carbon atom quantity can reach more than 20 or 20 (all being included), can be any 2～10 integer, the all identical 1 of all alkyl substituents wherein particularly.This class chelating tertiary amine comprises for example N,N,N (this is fit to), tetraethylethylenediamine, the basic diamines of inferior 14 (carbon), four octyl group hexanediamines, four-(mixed alkyl) quadrols etc.

(b) available ring diamines, as N, N, N ', N '-tetraalkyl-1,2-diamino-hexanaphthene, N, N, N ', N '-tetraalkyl-1,4-aminocyclohexane, N, N '-lupetazin etc.

(c) useful end of the bridge diamines comprises: sparteine, triethylenediamine etc.

Uncle's monoamine (as triethylenediamine) is not so effective usually in lithiation.But the homologue of end of the bridge monoamine such as 1-azabicyclo [2,2,2] octane and replacement thereof is effective.

Ether and alkali metal alcoholates be as suitable not as good as chelating amine at present aspect the activator of metal reaction, because they will contain functional group in graft reaction subsequently compound is attached to degree on the copolymer chain not as chelating amine.

The consumption of polarity metallization promotor will be enough to make metalation to take place, and for example whenever the amount lithium alkylide can be more preferably 0.1～10 equivalent with normal promotor more than 0.01～100 or 100, is preferably 1～3 equivalent.

Be generally in the multipolymer each vinyl-arene unit and need 0.001～3 normal lithium for reaching the required lithium consumption of desired lithiumation degree, each vinyl-arene unit is with 0.01～1.0 normal lithium in the multipolymer that preferably is modified at present.The mol ratio of active lithium and polar accelerant can for example change in 0.01～10.0 the scope.Best mol ratio is 0.5.

The consumption of lithium alkylide can be represented with the mol ratio of lithium and vinyl-arene.This mol ratio can be at each vinyl-arene unit 1 lithium alkylide of 1() to 1 * 10 ^-3Change in the scope of (per 1000 vinyl-arene unit 1 lithium alkylide).

Generally speaking, lithiation is preferably in the inert solvent (as stable hydrocarbon) and carries out.Aromatic solvent (as benzene) itself can lithiumation, therefore can disturb the due lithiumation of hydrogenation multipolymer.Solvent is convenient with the general ratio than about 5: 1～20: 1 of weight ratio of multipolymer.Hydrochloric ether, ketone and a pure kind solvent can destroy lithiation reagent because of them and should not adopt.

Lithiation can approximately-70 ℃～carry out under+150 ℃ the temperature, preferably adopt 25 ℃～80 ℃ temperature at present, the upper limit of temperature is subjected to the restriction of the thermostability of lithium compound.The lower limit of temperature is subjected to production cost to consider restriction, because speed of reaction is too low at low temperatures, is non-remunerative.Make lithiumation and subsequent reaction carry out that fully the required time is depended on mixing condition and temperature to a great extent.Generally, the time can be preferably 1 minute to 1 hour from about several seconds to 72 hour at present.

The next step of preparation modified block copolymer process be the hydrogenation multipolymer of own lithiumation in solution with a kind of mass treatment that can react with the lithium negatively charged ion, do not make its chilling by any way, because this can destroy the lithium active site.These reactive species are selected from the molecule that is called the electrophilic body.The most suitable electrophilic body is listed in front.These electrophilic bodies or contain desired functional group, or generating desired functional group when lithium negatively charged ion on the polymkeric substance reacts with being combined in.This contained functional group of class material comprises more following, but is not limited to these:

Present method also comprises the further react with of the segmented copolymer that makes modification.For example, the modified block copolymer of carboxylate-containing is converted into its carboxylic acid form, this is easy to carry out.

The present invention also relates to the impact-resistant polymer composition, it comprises polyamide thermoplastic, as nylon 6,6, or thermoplastic polyester such as poly terephthalic acid-1,4-butanediol ester (PBT) and polyethylene terephthalate (PET).These two kinds all is not only to have good intensity but also have fine inflexible material, and this makes them become useful structured material.But for specific application, a kind of polyamide thermoplastic or thermoplastic polyester may not provide the combination of desired properties.Therefore people are very interested in the method that overcomes this shortcoming.

A main drawback of polyamide thermoplastic and polyester is that its impact strength is poor, especially when drying especially like this.A kind of method of attractive especially raising thermoplastics impact strength is and other polymer blending.As everyone knows, rigidity plastics often can improve its impact strength by adding a kind of low modulus rubber immiscible with it.But in general, the physical blending of polymkeric substance is not a kind of flexible successful methods that improves polyamide thermoplastic and polyester.This is because the adhesive power between the immiscible polymkeric substance all is relatively poor usually.The result makes the interface between the blend components zone become serious weak area, produces nature and flows, and consequently is easy to produce mechanism collapse.

Those skilled in the art knows that the styrene-butadiene block copolymer of hydrogenation has the impact strength that makes plastics and improves required many performances.They have reduced TG transformation, the low modulus rubber phase that makes the plastics malleableize required.Because their degree of unsaturation is low, they can not degraded with the plastic blend of high processing temperature.In addition, they be better than other rubber part also show their contained blocks use and processing conditions under be microphase-separated.This microphase-separated produces physical crosslinking, makes it have elasticity under solid-state and molten state.Intensity mechanism usually is needed for obtaining toughness in the impact property of improving plastics is used in this.In addition, the melt elasticity performance that segmented copolymer is presented in the course of processing makes itself and another kind of polymkeric substance be dispersed in the common external phase structure stable, interpenetration under suitable condition very thinly, and when rubberresin blends being needs this stable finely divided structure.

The vinylbenzene of hydrogenation and butadiene block copolymer are widely used in the modification of polyolefine and polystyrene, and this just proves that it is effective Plastics Impact Modifiers.For these blends, the interface adhesive power is enough to reaching malleableize.

Much can make the desired characteristic of plastic impact improvement in performance though the segmented copolymer of hydrogenation has really, they still exist weak point when the dissimilar many material of those structures of modification and vinylbenzene or hydrogenation divinyl.The blend of this hydrogenation segmented copolymer and the dissimilar plastics of structure is normal because shortage interface surface of adherence is tough and tensile inadequately.

Making a method that produces the interface adhesive power between the hydrogenation segmented copolymer material different with structure is to enable the interactional functional moiety of the material different with structure to be connected on the segmented copolymer by chemical reaction.This interaction comprises chemical reaction, hydrogen bonding and dipole-dipole interaction.

Epslein is at United States Patent (USP) 4,174, public affairs-property agent in 358.But this patent and styrene-butadiene block copolymer unexposed or suggestion employing modification.

Once the someone proposed in the past, improved the shock strength of polymeric amide and polyester by the segmented copolymer that adds modification.US Patent specification 4,427,828 and International Patent Application Publication No. W083/00492 the blend composition of the segmented copolymer of polyamide thermoplastic or a polyester and a modification is all disclosed.Specifically, this segmented copolymer is the monovinylarene-conjugated diene block copolymer that contains the partial hydrogenation of anhydride moiety (being by aforesaid " ENE " reaction anhydride moiety to be linked on the segmented copolymer).

The present invention also provides 1 of a kind of selection hydrogenation by polyamide thermoplastic and heat-staple, modification, the shock-resistant blend composition that monovinylarene-conjugated diene block copolymer that 2 content are high is formed, having a kind of functional group in described segmented copolymer at least is grafted on the vinyl-arene block of multipolymer, and best impact-resistant polymer composition comprises:

(a) polymeric amide (number-average molecular weight is at least 5,000) 50-97%(weight) or thermoplastic polyester and (b) 3-50%(weight) the selection hydrogenation segmented copolymer by the functionalization of the inventive method preparation.

Polymeric amide parent resin in the malleableize composition of the present invention is being well-known in the art, and it comprises that those molecular weight are at least 5000 hypocrystalline that is referred to as nylon usually and amorphous resin.Suitable polymeric amide is included in US Patent specification 2,071,250; 2,071,251; 2,130,523; 2,130,948; 2,241,322; 2,312,966; 2,512,606 and 3,393, those polymkeric substance described in No. 210.Polyamide resin can get with diamines (containing 4～14 carbon atoms) condensation by the saturated dicarboxylic acid (containing 4～twelve carbon atom) of equimolar amount.Available excessive diamines is so that the many son ends of polymeric amide middle-end amido number carboxyl number.The example of polymeric amide comprises polyhexamethylene adipamide (nylon 66), polyhexamethylene azelaoyl amine (nylon 69), polyhexamethylene sebacamide (NYLON610), polyhexamethylene isophthaloyl amine and polyhexamethylene 12 (alkane) diamide (nylon 612), the polymeric amide that open loop by lactan makes, i.e. polycaprolactam, polylauryllactam, amino 11 (alkane) acid of poly--11-, bis(p-aminocyclohexyl) methane 12 (alkane) acid amides.The polymeric amide that also can adopt the terpolymerization by two kinds of polymkeric substance copolymerization or above-mentioned polymkeric substance (or its component) in the above-mentioned polymkeric substance to make in the present invention, as hexanodioic acid m-phthalic acid hexamethylene diamine copolymer or polyhexamethylene right-altogether-isophthaloyl amine.Preferably polymeric amide is a line style, and fusing point is more than 200 ℃.Shared weight ratio can be up to 97% in composition for polymeric amide, and for example 60～95%, but be preferably 70～95%, or narrower scopes are 75～90%, as 80～90%.

The used thermoplastic polyester of the present invention is generally crystalline texture, and fusing point is thermoplastic about more than 120 ℃, rather than heat cured.

The particularly useful polyester of one class is that the anhydride ester derivs of those lower alkyl esters, acyl fontanel or acyl fontanels that make di-carboxylic acid or di-carboxylic acid with the well-known method in present technique field and dibasic alcohol carry out condensation and the thermoplastic polyester that makes.

The aromatics and the aliphatic dicarboxylic acid that are applicable to polyester useful among preparation the present invention have: oxalic acid, propanedioic acid, Succinic Acid, pentanedioic acid, hexanodioic acid, suberic acid, nonane diacid, sebacic acid, terephthalic acid, m-phthalic acid, right-the carboxylic toluylic acid, right, right '-the dicarboxyl phenylbenzene, right, right '-the dicarboxyl sulfobenzide, right-the carboxylic phenylium, right-the carboxylic phenoxy propionic acid, right-the carboxylic phenoxybutyhc, right-carboxylic phenoxy group valeric acid, right-carboxylic phenoxy group caproic acid, right, right '-the dicarboxyl diphenyl propane, right, right '-dicarboxyl phenylbenzene octane, 3-alkyl-4-(β-carboxylic oxyethyl group) phenylformic acid, 2, the 6-naphthalic acid, 2,7-naphthalic acid etc.Also can adopt the mixture of di-carboxylic acid.Preferably adopt terephthalic acid.

Be applicable to that preparation comprises that to the dibasic alcohol of the useful polyester of the present invention carbonatoms is 2～12 straight-chain alkyl-sub-glycol, as 1,1, ammediol, 1,6-hexylene glycol, decamethylene-glycol, 1, the inferior dodecyl glycol of 12-etc.Aromatic diol can all replace or part replaces.The aromatics dicarboxylic compounds that is suitable for comprises: right-xylylene-glycol, and pyrocatechol, Resorcinol, the alkyl-substituted derivative of Resorcinol or these compounds.Another glycol that is suitable for is a 1,4 cyclohexane dimethanol.The most suitable glycol is that carbonatoms is 2～4 straight-chain alkyl-sub-glycol.

The polyester that is suitable for has polyethylene terephthalate, Poly(Trimethylene Terephthalate) and polybutylene terephthalate.Best polyester is a polybutylene terephthalate.Polybutylene terephthalate is a kind of crystalline copolymer, can be by 1, and 4-butyleneglycol and dimethyl terephthalate (DMT) or terephthalic acid polycondensation and get, and have following general formula:

N is 70～140 in the formula.The molecular weight of polyethylene terephthalate is about 20,000～25,000 usually.The method that is applicable to this polymkeric substance of preparation is in british patent specification 1,305, and is open in 130.

Poly-terephthalic acid butanediol ester on the market can (General Elietric obtains, and its trade name is VALOX from General Electric Corporation

Thermoplastic polyester.Other polymkeric substance of supplying on the market has the CELANEX of Celanese company

, the TENTITE of Eastman kodak company

VITUF with Goodyear chemical company

Other useful polyester comprises cellulose family.Here the cellulose ester of Cai Yonging is widely used as moulding compound, coating and film forming material, is well-known.These materials comprise solid thermoplastic nitrocellulose; rhodia (as secondary cellulose acetate, cellulose triacetate), cellulose butyrate; cellulose acetate butyrate; cellulose propionate, three capric acid Mierocrystalline celluloses, carboxymethyl cellulose; ethyl cellulose; Natvosol and acetylizad Natvosol (seeing " modern plastics encyclopedia " (Modern Plastics Encyclopedia), 1971-72,25-28 page or leaf and listed bibliography).

The another kind of polyester that is suitable for is poly-pivalolactone.Poly-pivalolactone is a kind ofly to have repetition ester structure unit and (be mainly-CH ₂-C(CH ₃) ₂-C(O) O-) simple linear polymer is promptly by the structural unit of pivalolactone derivative.Preferably polyester is the homopolymer of pivalolactone.But other β-Bing Chunsuanneizhi class that also comprises pivalolactone and no more than 50 molecular fractions (preferably no more than 10 molecular fractions) is (as β-Bing Chunsuanneizhi, α, α-diethyl-β-Bing Chunsuanneizhi and Alpha-Methyl-α-ethyl-β-Bing Chunsuanneizhi) multipolymer.Term " β-Bing Chunsuanneizhi class " means on the beta carbon of β-Bing Chunsuanneizhi (2-oxetanone) and lactonic ring thereof is not with substituent derivative.The β-Bing Chunsuanneizhi class of preferentially selecting for use is that those contain on the alpha-position of carboxyl-tertiary carbon or quaternary carbon atom.That especially be suitable for is α, α-dialkyl group-β-Bing Chunsuanneizhi, and wherein each alkyl contains 1～4 carbon atom respectively.The examples of monomers that is suitable for has:

α-ethyl-Alpha-Methyl-β-Bing Chunsuanneizhi

Alpha-Methyl-α-sec.-propyl-β-Bing Chunsuanneizhi

α-ethyl-α-normal-butyl-β-Bing Chunsuanneizhi

α-chloromethyl-Alpha-Methyl-β-Bing Chunsuanneizhi

α, α-two (chloromethyl) β-Bing Chunsuanneizhi and

α, alpha-alpha-dimethyl-β-Bing Chunsuanneizhi (pivalolactone)

Generally can consult US Patent specification 3,259,607; 3,299,171; With 3,579,489.The molecular weight of these poly-pivalolactones surpasses 20,000, and fusing point is more than 120 ℃.

Another useful polyester is a polycaprolactone, and typical poly-(ε-caproic acid lactone) is simple linear polymer substantially, and its repeating unit is:

These polymer properties are similar to poly-pivalolactone, available similar polymerization process preparation.Generally can consult US Patent specification 3,259,607.

The copolyesters of line style and branched polyester and dibasic alcohol and terephthalic acid or m-phthalic acid is supplied on market and is had for many years, and by people such as Whinfeld in US Patent specification 3,465, in 319 and Pengilly in US Patent specification 3, described in 047,539.

Thermoplastic polyester as PBT and PET, but is useful extrusion molding material, can make the over-all properties product of good (comprising intensity and rigidity).But the shock strength of these materials also needs to improve.

Composition of the present invention also can contain polyamide thermoplastic except that containing thermoplastic polyester.

Malleableize preparation of compositions method of the present invention is in a closed system polymeric amide or polyester to be become a uniform mixture with at least a modified block copolymer melt blending, this operates in the multiple screw extruder (as common extruding 2-5 knead parts and the Werer Pfleiderer forcing machine of at least one reverse pitch with the generation high shear force) or carries out in other plasticator (as Braberder, Banbury machine etc.) commonly used.The other method of preparation blend composition is that elder generation's co-precipitation from solution is come out, and then with each component blend or dried mixing, then with the method for extruding dry mixture is carried out melt extrusion.

The preparation method of modified polyamide and polyester and resin blend of the present invention is with 50～97%(weight) (be preferably 70～95%, preferably 75～90%) polymeric amide or polyester and 3～50%(weight) segmented copolymer of (be preferably 5～30%, preferably 10～25%) functionalization carries out melt blending.

Composition of the present invention can be with one or more typical additives such as antioxidant, thermo-stabilizer, ultraviolet degradation inhibitor, annotate lubrication prescription and releasing agent, tinting material (comprising dyestuff and pigment), fibrous and particulate filler and toughener, granulating agent, softening agent comes modification.

Stablizer can add in any stage in the thermoplastic compounds preparation process.Preferably add earlier to prevent that composition from beginning degraded under the situation that does not have protection.Stablizer must be compatible with composition.

The oxidation inhibitor and the thermo-stabilizer that are applicable to material of the present invention comprise those materials that are generally used for addition polymer.They comprise I family metal halide, as sodium, potassium, lithium and cuprous fontanelle compound (as muriate, bromide, iodide), sterically hindered phenol, quinhydrones and above-mentioned various substituent and and use thing, consumption can reach 1% of polymeric amide or weight polyester.

Ultra-violet stabilizer also is generally used for those materials of addition polymer, and consumption can reach 2.0% of polymeric amide weight.The example of ultra-violet stabilizer have separately the Resorcinol that replaces, salicylate, benzotriazole, benzophenone etc.

The lubricant that is suitable for and the consumption of releasing agent can reach 1.0% of composition weight, and its example has stearic acid, stearyl alcohol, stearylamide, organic dye has aniline point etc., pigment such as titanium dioxide, Cadmium Sulfide, Cadmium Sulfide selenide, phthalocyanine, ultramarine, carbon black etc., and example fibrous and particulate filler and toughener has carbon fiber, glass fibre, soft silica, asbestos, Calucium Silicate powder, pure aluminium silicate, magnesiumcarbonate, kaolin, chalk, silica powder, mica, feldspar etc., consumption can reach 50% of composition weight; The example uranium talcum of nucleator, calcium chloride, phenyl-phosphonic acid sodium, alumina, polytetrafluoroethylfine fine particle etc.; The example of softening agent has dioctyl phthalate (DOP), dibenzyl phthalate, and butyl benzyl phthalate, hydrocarbon ils, N-n-butylbenzene sulphonamide, adjacent-and right-toluene ethyl sulfonamide etc., consumption can reach about 20% of composition weight.The consumption of tinting material (dyestuff and pigment) can reach constituent weight about 5.0%.

Relate to the melt blending part in this specification sheets and claims, except as otherwise noted, the consumption of polymeric amide, polyester or segmented copolymer all represents with weight percentage, in other words, and the weight percentage of material therefor gross weight when being melt blending.

Following example will further specify the present invention

Example 1

The raw materials used polymkeric substance of this example is styrene-ethylene/butylene-styrene (S-E/B-S) type segmented copolymer (referring to polymerization ofathe reactants thing A here).The molecular weight of polymerization ofathe reactants thing A is about 50,000, contains 30% polystyrene.

In a typical test, with 45.36 kilograms the polymer cements (hexanaphthene that contains polymer A, solids content is 5%) in order to diamines (Tetramethyl Ethylene Diamine, TMEDA) do promotor the second month in a season-butyllithium reagent (1.1 moles of reagent, 1.8 moles of promotor) carries out lithiumation under 60 ℃.Metallization reaction produces a kind of thixotropic semi-solid clay that has rapidly, and the stirring mechanism (spiral type) of reactor can't be rotated in 3-4 minute again.The lithiumation polymer cement is divided into two parts, a copy of it DO ₂Chilling, remainder are that 3.8 centimetres conduit is transported to one and contains excessive CO by a diameter ₂In the container of the tetrahydrofuran (THF) (THF) of (1.36 kilograms), with carboxylation product handle with acetate (85 gram, 1.4 moles), carry out devaporation at last, obtain polymkeric substance chip white, functionalization more than 1.81 kilograms.The analytical results of carboxylation product shows and includes-CO ₂H0.84%(weight), contain-CO ₂-0.29%(weight), the total content of the carboxylate that combines with polymkeric substance is a 1.13%(weight).

To through D ₂Those equal portions that O handles carry out the deuteron magnetic resonance analysis, found that, D mainly be present in aromatic ring between in position and the contraposition (account for D total amount 90%), the rest part of mark be on benzyl or allylic positions (account for D total amount 10%).Nmr analysis can't be distinguished allyl group position and benzyl position.Therefore, mark main (at least 90%) even be present in all probably in the polystyrene block of polymkeric substance.We can know all lithiations (at least 90%) by inference and occur in the polystyrene block from this mark test.Therefore in fact all carboxylations also must occur in those positions.

The carboxylate (lithiumation efficient) of from the product of this test, finding have 50% second month in a season-butyllithium reactant to be converted into and combining with polymkeric substance.In the end in the product, per 26 parts of carboxylate salt (CO- ₂) contain 74 parts of acid (CO ₂H).

Example 2-14

Example 2-14 method therefor and example 1 are roughly the same, but have done some modifications, see Table 1.

Polymerization ofathe reactants thing B is similar to polymer A, and molecular weight is about 67,000.Polymerization ofathe reactants thing C is similar to polymer A, and molecular weight is about 181,000, and polystyrene content is 33%.Polymerization ofathe reactants thing D is-S-E/P type segmented copolymer, and total molecular weight is about 98,000, and polystyrene content is 37%.

In all these examples, when polymer A, B and C carried out lithiumation, viscosity all increased very soon.In some example, lithiated product can not placed the long period under the condition of stirring.The viscosity of clay does not significantly increase during polymkeric substance D lithiumation.

The same with the result of example 1, to using D ₂The a various products of that of O chilling carry out the deuteron magnetic resonance analysis, and the result shows that mark mainly is in the polystyrene block of polymkeric substance.The results are shown in Table 2 for these.

Each deuterated sample is all analyzed with gel permeation chromatography.The molecular weight of gained is significantly different with the molecular weight of original not metallized polymeric.This shows that metallization does not make these polymkeric substance produce any degraded (as chain rupture) or crosslinked.

The control experiment that the reaction technology of use-case 1 and S-rubber-S segmented copolymer (the rubber here is undersaturated substantially) carry out shows that the lithiumation of these reactants in styrene block and in the diblock rubber do not have much difference, respectively accounts for about 50%.These at random the functionalization product be not desired.(seeing Table I, II)

Example 15

By following step the modified block copolymer of example 14 is converted into hydroxy acid salt: 50 gram polymkeric substance are dissolved in the mixture (90: 10) of 500 gram hexanaphthenes and THF.Then heat 1 mole of LiOH aqueous solution of 4.3 grams.Mixture left standstill 24 hours.Make polymer precipitation with methyl alcohol then, and carry out drying under the 1 atmospheric pressure to regain polymkeric substance being lower than.Sample is carried out infrared analysis, and the result shows that acid functional group is converted into lithium salts functional group fully.The absorption band of salt appears at 1560～1600 centimetres ^-1The place, the absorption band of acid then appears at 1690 centimetres ^-1The place.

Example 16

This example is that hydroxy functional group is attached on the stock polymer.Raw materials used polymkeric substance is polymerization ofathe reactants thing B.

In glass reactor, 100 gram stock polymers are dissolved under argon purge in 100 milliliters of hexanaphthenes.Then add 1.02 millinormal amounts and add TMEDA by every gram polymkeric substance.Then with the second month in a season-the butyllithium titration to be to remove the impurity in the mixture.Reactant is heated to 50 ℃, adds 0.51 millinormal amount by every gram polymkeric substance and add the second month in a season-butyllithium once more.Add 1000 milliliters of distilled THF, solution was stirred 16 hours down at 25 ℃.This mixture was kept 70 minutes down at 40～45 ℃.Make oxyethane bubbling in reactor then, and compound was stirred 10 minutes down at 45 ℃.At last by every gram polymkeric substance add 1 millinormal amount with HCI(in methyl alcohol) add reactor.Make polymer coagulation become the 2-propyl alcohol and regain, and use methanol wash.A part of polymkeric substance is carried out drying being lower than under 40 ℃ under the 1 atmospheric pressure.

In order to analyze this hydroxylated polymkeric substance, polymkeric substance is reacted with maleic anhydride in diisopropylbenzene(DIPB) under 150～160 ℃, OH functional group is converted into acid.Reaction product in methyl alcohol, precipitate and with 70 ℃ of water washings to remove unreacted maleic anhydride.The infrared analysis result shows at 1730 centimetres ^-1There are the peculiar carboxyl bands of a spectrum of Malaysia ester at the place.

Then polymkeric substance is carried out drying in 50 ℃ being lower than under the 1 atmospheric pressure.Make indicator with phenolphthalein, methanol solution titration half maleic acid ester with potassium methylate draws every gram polymkeric substance and contains 0.18 millinormal acid, and this shows that every gram polymkeric substance contains 0.18 milligramequivalent-OH base in original modified block copolymer.

Measure with following test method under the drying regime of molded sample in the following example after molding comes out:

Notched izod impelling strength: ASTM D-256-56

Example 17-19 and simultaneous test A-D

Raw materials used polymkeric substance is for containing 29%(weight) vinylbenzene, molecular weight is 66,000 styrene-ethylene/butylene-styrene block copolymer.2270 gram polymkeric substance are dissolved in 56.8 liters of hexanaphthenes.Mixture is placed 7.6 liters of stainless steel pressurized reactors, and be forced into 1.7 * 10 ⁵About handkerchief.Add 0.8 millinormal amount by every gram polymkeric substance then and add Tetramethyl Ethylene Diamine.Then a small amount of (0.5 milliliter) 1 (indicator) is added reactor.Increment adds the second month in a season-butyllithium till producing yellow again, and this shows free from foreign meter.

Reactant is heated to 60 ℃ then.Then, add 0.4 millinormal amount by every gram polymkeric substance and add the second month in a season-butyllithium once more.React after 2.5 hours, the reactant in the reactor is moved into another reactor of band whipping appts.This reactor contains 0.9～1.4 kilogram of dry ice (solid CO ₂), 37,9 liters of tetrahydrofuran (THF)s and 18.9 liters of ether.With solution stirring 30 minutes.Then the solution of 85 gram acetate in α-propyl alcohol is added reactor.With this solution stirring 16 hours.Then with the vaporizing extract process property regained segmented copolymer.

Polymkeric substance is carried out infrared analysis, 1690 centimetres ^-1The absorption peak at place shows has the bonded carboxylic acid to have 1560～1600 centimetres ^-1Place's absorption peak shows has bonded carboxylic acid lithium salts to exist.Make indicator with phenolphthalein, carry out colorimetric titration with the 0.01NKOH methanol solution, the amount that records bonded acid is a 0.3%(weight) COOH.Polymkeric substance carries out infrared analysis after repeatedly washing with the hydrochloric acid alcoholic solution, and the result shows that salt all is converted into acid.The polymkeric substance of cleaning is carried out titration, and the result shows that the amount of combined acid is a 0.4%(weight) COOH.

The used polyamide thermoplastic of this example is the nylon of supplying on a kind of market 6,6, the trade name of Zytel101(Dnpont company moulding compound).Before all procedure of processings begin.Nylon 6,6 and blend thereof are all following dry 4 hours at 120 ℃ under the situation that is lower than 1 atmospheric pressure and nitrogen purging.

Nylon 6,6 all is to prepare in the moving twin screw extruder of the corotation of one 30 mm dia with the blend of unmodified segmented copolymer and modified block copolymer.The component of blend earlier in polyethylene bag lift-over and then add in the forcing machine carrying out pre-mixing.Melt temperature in the forcing machine is 270 ℃ at charging zone, is 285 ℃ at the extrusion die place.The screw speed that adopts is 300 rev/mins (rpm).Extrudate carries out granulation and injection mould is moulded sample.Prescription and physicals are shown in the table III.(seeing Table III)

The shock strength that example 17-19 shows composition of the present invention has than the shock strength of the blend of polyamide thermoplastic or polyamide thermoplastic and unmodified segmented copolymer and exceeds unexpected improvement.

Example 20-22 and simultaneous test E-H

The used thermoplastic polyester of this example is the PBT on the market, the moulding compound of Valox310(GE company).Before all procedure of processings began, PBT and blend composition thereof were all following dry 4 hours at 120 ℃ under the situation that is lower than 1 atmospheric pressure and nitrogen purging.Person used among modified block copolymer and the example 17-19 is identical.

The blend composition of PBT and unmodified segmented copolymer and modified block copolymer all is to prepare in the moving twin screw extruder of the corotation of one 30 mm dia.The component of blend earlier in polyethylene bag lift-over and then add in the forcing machine carrying out pre-mixing.Melt temperature in the forcing machine is 230 ℃ at charging zone, is 240 ℃ at the extrusion die place.The screw speed that adopts is 300rpm.Extrudate carries out granulation and injection mould is moulded sample.Prescription and physicals are shown in the table IV.(seeing Table IV)

The shock strength that example 20-22 shows composition of the present invention has than the shock strength of the blend of thermoplasticity polyester or thermoplastic polyester and unmodified segmented copolymer and exceeds unexpected improvement.

The table I contains the preparation of the Kranton G polymkeric substance of lithium carboxylate functional group

The reaction conditions product analysis

Carboxylate content lithiumation acid/salt during example polymkeric substance S-Bu reaction

(%) weight efficiency between type-Li

When the theoretical end of (mole) (branch) acidifying % finishes

Post polymerization thing during value

2 A 1.13 60 2.25 1.12 1.39 62 81/19

3 A 1.13 60 2.25 0.21 0.22 10 95/5

4 A 1.13 60 2.25 0.60 1.04 46 58/42

5 B 1.13 1 2.25 - 0.94 42 10/90

6 B 1.13 2 2.25 0.13 1.00 44 13/87

7 B 0.38 60 0.75 0.46 0.43 58 99/1

8 B 0.38 60 0.75 0.28 0.27 36 99/1

9 C 0.38 4 0.75 0.22 0.33 44 67/33

10 C 0.38 10 0.75 0.31 0.33 46 94/6

11 D 1.13 60 2.25 0.92 1.15 51 80/20

12 D 1.13 30 2.25 0.36 0.24 11 99/1

13 D 1.13 60 2.25 1.15 1.39 62 83/17

14 B 0.9 150 - 0.44 - - -

The table II

The position that deuterate accounts for

The deuterium-labelled position of instance number (carboxylate)

(%) benzyl of aromatics, allylic (%)

2 91 9

3 93 7

4 92 8

The table III

Example 17 18 19

Simultaneous test A B C D

Nylon 6,6 100 90 80 70 90 80 70

Unmodified segmented copolymer-10 20 30---

Modified block copolymer----10 20 30

The back 43 48 53 64 53 107 288 3.2 the millimeter molding comes out

Dry sample room temperature otch outstanding

Arm beam type impelling strength (J/m)

The table IV

Example 20 21 22

Simultaneous test E F G H

PBT 100 90 80 70 90 80 70

Unmodified segmented copolymer-10 20 30---

Modified block copolymer----10 20 30

3.2 millimeter room temperature

Notched izod impelling strength (J/m) 37 48 75 91 107 1,062 1148

Claims (46)

1, impact-resistant polymer composition comprises:

A) 50-97% polymeric amide (number-average molecular weight is at least 5000) or thermoplastic polyester and

B) the segmented copolymer functionalization of 3-50% (weight), that select hydrogenation, wherein said segmented copolymer is that general formula is B _n(AB) ₀A _pBut selection hydrogenation segmented copolymer under the alkyl lithium compounds effect, contact the segmented copolymer of the main polymer chain of the band grafting molecule that the back generates with at least one electrophilic grafting molecule or electrophilic body, n is 0 or is at least 1 integer in the formula, o is an integer, be at least 1, p is 0 or is at least 1 integer, A is mainly poly-mono-alkenyl-aromatic hydrocarbons block, and B is mainly a poly-conjugated-diolefin block before hydrogenation.

2, impact-resistant polymer composition according to claim 1, wherein the content of polymeric amide or polyester is 70% to 95%(weight).

3, impact-resistant compositions according to claim 2, wherein the content of polymeric amide or polyester is 75% to 90%(weight).

4, according to each described impact-resistant polymer composition in the claim 1 to 3, polymeric amide wherein is a nylon 6.6.

5, according to each described impact-resistant polymer composition in the claim 1 to 3, that polyamide resin wherein is selected from polyhexamethylene adipamide, polyhexamethylene sebacamide, polycaprolactam, polyhexamethylene isophthaloyl amine, polyhexamethylene is right-altogether-isophthaloyl amine and compound and multipolymer.

6, according to each described impact-resistant polymer composition in the claim 1 to 3, wherein polyester is a polybutylene terephthalate.

7, according to each described impact-resistant polymer composition in the claim 1 to 3, wherein polyester is a polyethylene terephthalate.

8, according to the described composition of claim 1, wherein the molecular-weight average of each block A is 1000 to 115000.

9, composition according to claim 8, wherein the molecular-weight average of each block A is 500 to 60000.

10, composition according to claim 1, wherein the molecular-weight average of each B block is 20000 to 450000.

11, according to the composition described in the claim 10, wherein the molecular-weight average of each B block is 35000 to 150000.

12, composition according to claim 1, wherein block A accounts for 1% to 95% of multipolymer gross weight.

13, composition according to claim 12, wherein block A accounts for 1% to 40% of multipolymer gross weight.

14, composition according to claim 1, wherein the degree of unsaturation of B block is less than 20% of original degree of unsaturation.

15, composition according to claim 14, wherein the degree of unsaturation of B block is less than 10% of original degree of unsaturation.

16, composition according to claim 15, wherein the degree of unsaturation of B block is less than 5% of original degree of unsaturation.

17, composition according to claim 1, wherein the degree of unsaturation of block A is at more than 50% of its original degree of unsaturation.

18, composition according to claim 17, wherein the degree of unsaturation of block A is at more than 90% of its original degree of unsaturation.

19, composition according to claim 1, wherein the degree of unsaturation of block A is at below 25% of its original degree of unsaturation.

20, composition according to claim 1, wherein the average degree of unsaturation of hydrogenation segmented copolymer has been reduced to below 20% of its original value.

21, composition according to claim 1, conjugated diolefine wherein is a 1,3-butadiene.

22, according to the composition described in the claim 21, wherein 35% to 50% condensed butadiene unit is 1, the 2-configuration.

23, composition according to claim 1, before hydrogenation, polymeric block A is the polymer blocks of mono-alkenyl-aromatic hydrocarbons.

24, composition according to claim 23, mono-alkenyl-aromatic hydrocarbons wherein is vinylbenzene.

25, composition according to claim 1, segmented copolymer wherein is a styrene-ethylene/butylene-styrene block copolymer.

26, according to each described composition in the claim 1 to 3, electrophilic body wherein is a carbonic acid gas.

27, composition according to claim 1, electrophilic body wherein is an oxyethane.

28, composition according to claim 1, electrophilic body wherein is selected from aldehyde, ketone and carboxylic acid and salt and ester.

29, composition according to claim 1, electrophilic body wherein is an epoxide.

30, composition according to claim 1, electrophilic body wherein is a sulphur.

31, composition according to claim 1, electrophilic body wherein is a sulphur.

32, composition according to claim 1, electrophilic body wherein are isocyanate (esters).

33, composition according to claim 1, electrophilic body wherein is siliceous molecule.

34, composition according to claim 1, electrophilic body wherein are sulfonate (esters).

35, composition according to claim 1, grafting molecule wherein contains one or more functional groups.

36, composition according to claim 35, functional group wherein is carboxylic acid or its salt or ester.

37, composition according to claim 35, functional group wherein is a ketone.

38, composition according to claim 35, functional group wherein is pure and mild alkoxide.

39, composition according to claim 35, functional group wherein is an amine.

40, composition according to claim 35, functional group wherein is the functional group of silicon atoms.

41, composition according to claim 35, functional group wherein is a mercaptan.

42, composition according to claim 35, functional group wherein is a borate.

43, composition according to claim 35, functional group wherein is an acid amides.

44, according to each described composition in the claim 35 to 43, wherein the content of grafting molecule is 0.02% to 20%(weight).

45, according to the described composition of claim 44, wherein the content of grafting molecule is 0.1% to 10%(weight).

46, according to the described composition of claim 44, wherein the content of grafting molecule is 0.2% to 5.0%(weight).