BACKGROUND

This invention relates to thermoplastic elastomers.

Thermoplastic elastomers, which are often referred to as TPE's, are well known. The TPE's in general use contain (i) polymeric blocks (usually referred to as "hard" blocks or A blocks) which (a) are amorphous and have a second order transition point,T _g h, which is well above room temperature, or (b) have a crystalline polymer backbone and have a crystalline melting point, T _m h, which is well above room temperature, and (ii) amorphous polymeric blocks (usually referred to as "soft" blocks or B blocks) which have a glass transition point, T _gs , which is well below room temperature. Each soft block is linked to at least two hard blocks, so that at temperatures between T _gs and T _m , or T _gs and T _g h, the amorphous B blocks are tied together, resulting in elastomeric behavior. Above T _m or Tg , melting or softening of the hard blocks permits viscous flow of the polymeric chains, resulting in thermoplastic behavior. Known TPE's are described for example in U.S. Patent Nos. 4,260,659 (Gobran), 4,361,526 (Allen), 4,483,978 (Manser), 4,551,388 (Schlademan), 4,554,324 (Husman), 4,656,213 (Schladman), 4,764,586 (Manser), 4,778,852 (Futamura), 4,806,613 (Wardle), 4,830,855 (Stewart), 4,919,737 (Biddle et al), 4,952,644 (Wardle et al), and 4,976,794 (Biddle et al) and in the articles in Polymer, 22 (7), 1233-1239 (1988) Kallitsis et al; J. Appl. Poly. Sci 3_7_ (1), 267-281 (1989) Murphy et al; J. Poly. Sci, Part A, Poly Chem, 2£ (9) 2393-2401 (1990) Talukder et al; Makromol Chem, 190_, 1069-1078 (1989) Khan et al, 19_i, 603-614, 615-624, and 2341- 2354 (1990) Fakirov et al, and 19J.2355-2365 (1990) Gogeva; and Macromolecules i£ (2), 123-127 (1985) Miyamoto et al, and 23, 333-337 (1990) Chow.

In our earlier International Patent Application No. PCT/US92/08508 (Docket 9213.1-PCT), filed October 8, 1992, published April 15, 1993, as Publication No.

WO 93/07194 (Docket 9213.1-PCT), we described and claimed thermoplastic elastomers (TPE's) which contain hard (A) blocks comprising side chain crystallizable (SCC) moieties which render the block crystalline, and which have a melting point T _q , and soft (B) blocks which are amorphous and have a T _gs which is less than (Tq-10)°C. That earlier application

had not been published on the priority date of this application (April 14, 1993), and the TPE's described therein are not, therefore, regarded as known TPE's in this application.

SUMMARY OF THE INVENTION

This invention relates to TPE's comprising A blocks, or B blocks, or both A blocks and B blocks, which are crystalline and in which at least a part of the crystallinity results from the presence of crystallizable side chains. Such crystalline blocks are referred to herein as SCC blocks. TPE's containing SCC A blocks and amorphous B blocks are described and claimed in our earlier application referred to above. TPE's containing SCC A blocks and crystalline B blocks (which may also be SCC blocks) are novel and as such form part of the present invention; they are referred to herein as "the novel TPE's". The invention also includes a wide range of novel processes, compositions, shaped articles and assemblies which make use of (1) the novel TPE's, (2) the TPE's described in the earlier application, and (3) TPE's described in the prior art.

We have discovered that the novel TPE's have the same advantages as the TPE's described in the earlier application. Like the TPE's of the earlier application, they can exhibit a much more rapid change in viscosity in the region of the crystalline melting point of the side chains in the TPE (referred to herein as T _q ) than is exhibited by known TPE's in the region of T _m h or Tg . This results in a number of important advantages. One is that the novel TPE's can be melt processed at temperatures not far above T _q , e.g. below about (T _q + 10)°C, typically below 100°C, for example below 75°C and even below 50°C, whereas known TPE's are typically melt processed at temperatures at least 40°C above T _m h or Tgh, usually above 100°C. This is particularly useful when the TPE is preferably or necessarily maintained at a temperature below a critical limit (referred to herein as T _cπt ), for example when the TPE is associated with a thermally responsive substance which may undergo, at a temperature above T _c ή ^an undesirable change. The substance may be for example in the form of (i) solid particles dispersed within the TPE, e.g. particles of an explosive solid, or a pharmaceutical or agricultural chemical, or (ii) a substrate which is contacted by the TPE, e.g. a vessel in a living animal into which the TPE has been injected or otherwise placed, or (iii) a solid or a liquid which is encapsulated by the TPE. Another advantage is that the novel TPE's can be used as carriers (including encapsulants) for substances which are at least partially protected against physical and/or chemical damage by the TPE at temperatures substantially below and approaching T _q . The hard blocks in the

TPE will begin to melt at a temperature T _Q which is somewhat below T _q , e.g. 3-12°C below Tq. As the temperature is increased from T _D to Tq, there is a rapid change in the protection provided by the TPE, and above Tq the substance may be released entirely from the TPE. For example, an agricultural chemical surrounded by the TPE can be applied while the ambient temperature is below T _q and will be released when the ambient temperature exceeds Tq. Similarly a seed coated with the TPE will not germinate until the ambient temperature approaches or exceeds T _q .

Another important advantage shown by the novel TPE's (and also by the TPE's in the earlier application) is that T _q can be closely controlled through selection of the crystallizable moieties in the side chains. For a given crystallizable moiety, T _q is mainly dependent on the length of the crystallizable moiety, and changes by at most a few °C, e.g. less than 5°C, with changes in the molecular weight of the A block. In the known TPE's, by contrast, T _m h or Tgh changes substantially with changes in the molecular weight of the A block. In the novel TPE's, therefore, it is possible to change the physical properties of the TPE (e.g. the elongation, modulus and tensile strength) without substantially changing T _q , by changing the total molecular weight of the TPE and/or the molecular weight of the A blocks and/or the relative amounts of the A and B blocks.

The novel TPE's also show a relatively small difference between T _q and the crystallization peak on a DSC curve as the TPE is cooled.

Another very important advantage of the novel TPE's is that the presence of the SCC A blocks results in improved shear strength. Furthermore, we have discovered that this advantage is also shown by the TPE's described in the earlier application. In addition, we have discovered that for both the novel TPE's of this application and the TPE's of the earlier application, shear strength can be yet further improved by mixing the TPE with a relatively low molecular weight and low melting crystalline additive, particularly an SCC polymer. The crystalline additive must be intimately mixed with the TPE, preferably by mixing the TPE and the additive in the melt or in a common solvent. Particularly good results are obtained when the SCC blocks in the TPE and in the additive are structurally similar, and we believe that the improved shear strength results from co-crystallization of the additive and the SCC blocks. Thus a preferred combination is a TPE containing SCC blocks comprising polymethylene or poly (substituted methylene) groups and an SCC additive comprising polymethylene or poly (substituted methylene) groups. The additive

and the amount thereof are preferably such that the composition has a shear strength which is at least 1.3 times, particularly at least 2 times, especially at least 3 times, the shear strength of the composition which is identical except that it does not contain the additive. The crystalline additive preferably has a number average molecular weight of less than 25,000, or a weight average molecular weight of less than 25,000, or both.

The advantages noted above make the TPE's with SCC hard blocks (and either crystalline or amorphous soft blocks), and mixtures thereof with crystalline additives, particularly suitable for use as pressure-sensitive adhesives (PSA's) and as hot melt adhesives. The TPE, or mixture thereof with a crystalline additive, can be the sole polymeric ingredient(s) of the adhesive, or can be mixed with other polymeric ingredients. For example, a conventional PSA can be modified by addition of the TPE or mixture of TPE and additive. The adhesive preferably contains 25 to 100%, particularly 75 to 100%, of the TPE, and 0 to 50%, preferably 1 to 40%, of the additive. PSA's for use in the medical field for attachment to human skin preferably contain 20 to 35% of the additive. PSA's for use in other fields preferably contain less than 15%, e.g. 1 to 5%, of the additive. The adhesive can also contain additives such as tackifiers, plasticizers, fillers, stabilizers and pigments. PSA's which contain the crystalline additive have the valuable property that they have reduced adhesive strength when heated to temperatures approaching or above the crystalline melting point of the additive, as discussed in Schmitt et al US Apphcation Nos. 07/829494 and 07/928,800 and the corresponding PCT Application No. US92/01153, publication No. WO 92/13901, the disclosures of which are incorporated herein for all purposes and to which reference should be made in particular for disclosure of crystalline additives, suitable substrates for PSA composites and uses of PSA composites.

The soft blocks in the novel TPE's can also be SCC blocks, and TPE's containing both SCC soft blocks and SCC hard blocks are particularly useful in the form of films and other shaped articles which are heat-sealed to other polymeric articles. The TPE undergoes a rapid change in its physical properties, including its permeability to at least some gases and vapors, e.g. O2, CO2 and water vapor, in the region of T _ms , but will retain substantial strength until heated to a temperature in the region of T _q , when it will again undergo a rapid change in its physical properties, including its heat sealability. The repeating units of the different SCC blocks can be selected to provide a change in permeability (or other property) over a desired temperature range, and to provide a hard block which, above T _m h» will be

compatible with the other polymeric material to which the TPE is to be heat sealed. In this way, it is possible to make a TPE which is sufficiently flexible at 0°C, which undergoes a marked change in permeability in the range of 0°C to 40°C, which retains adequate physical strength at temperatures up to T _q (or close to it) and which can be melt extruded and heat sealed at temperatures not far above T _q , e.g. 60° to 100°C. If desired, the physical strength of the TPE can be improved by crosslinking, but this is not generally necessary. Such a TPE can be particularly useful as a packaging material, e.g. for actively respiring biological material, as disclosed in our earlier International Application No. PCT/US91/09218 (docket 9209 PCT) filed December 6, 1991, the disclosure of which is incorporated herein for all purposes and to which reference should be made for details of this aspect of the invention.

We have also discovered that TPE's containing SCC soft (B) blocks have important and previously unrealized properties which make it possible to use such TPE's in ways which are novel and surprisingly valuable, even when the A blocks are not SCC blocks and the TPE is in itself known for use in other ways. For example, such TPE's can be used to provide pressure-sensitive adhesives (PSA's) with very valuable properties, to provide films and other shaped articles which can be heat-sealed to other articles, and to provide hot melt adhesives.

In a first aspect, this invention provides novel TPE's containing SCC hard (A) blocks and crystalline soft (A) blocks. These novel TPE's preferably comprise polymeric molecules which comprise

(i) polymeric A blocks which (a) are crystalline and have a melting point T _q , and

(b) wherein at least one of the A blocks comprises a side chain comprising crystallizable moieties which render the block crystalline; and (ii) at least one polymeric B block which is linked to at least two A blocks and which is crystalline and has a melting point T _ms which is less than (T _q -

10)°C.

Any process can be employed to make the novel TPE's of the present invention. However, particularly useful processes, which provide the second aspect of the present invention, are the processes I to IV disclosed in our earlier International Patent Application

No. PCT/US92/08508 (Publication No. WO 93/07194), to which reference should be made for details, bearing in mind that the B blocks must be crystalline and can also be SCC blocks.

In a third aspect, this invention provides a composition, shaped article or assembly which comprises a novel TPE as defined above and a second component which is associated with (e.g. is mixed with, is surrounded (e.g. encapsulated) by, surrounds or provides a substrate for) the TPE. In one preferred embodiment, the second component is a thermally responsive substance which undergoes a thermally induced change at a temperature T _cr j _t which is above the temperature at which the TPE can conveniently be melt processed. Because the novel TPE's can be melt-processed at temperatures close to Tq, generally below (T _q + 60)°C, often below (T _q + 40)°C, and even lower, they are superior to known TPE's, which are usually melt processed at temperatures well above T _g h or T _m h. Tcπ _t is preferably above (Tq + 10)°C, e.g. (T _q + 10)°C to (T _q + 40)°C or (T _q + 60)°C.

In a fourth aspect, this invention provides a process for making a shaped article, which process comprises

(A) melting a novel TPE as defined above,

(B) dispersing an additive in the molten TPE, (C) shaping the dispersion from step B, and

(D) cooling the shaped article from step C to a temperature below T _q .

In a fifth aspect, this invention provides a process for releasing the second component from a composition, shaped article or assembly of the third aspect of the invention, which process comprises heating the composition, article or assembly by means of heat which is (i) generated by a mammalian body or (ii) generated artifically, e.g. by an electrical or other heater or by an engine or electrical motor, and/or (iii) conveyed artifically to the TPE. The heat may be conveyed to the TPE by convection, conduction or radiation, but is preferably conveyed by means of a stream of heated fluid, e.g. heated air or a body fluid, which also assists in removal of the second component from the TPE.

The sixth, seventh, and eighth aspects of the invention are based upon our discovery that TPE's containing SCC blocks (which may be hard blocks or soft blocks or both) have valuable properties which are not disclosed in the prior art or in the earlier International Application No. PCT/US92/08508.

In a sixth aspect, this invention provides a composition which is suitable for use as (or in the production of) a pressure-sensitive adhesive (PSA) and which comprises a TPE in which the A blocks, or the B blocks, or both, are SCC blocks. Particularly useful PSA compositions comprise a mixture of the TPE with (a) a crystalline polymer additive, preferably a side chain crystallizable (SCC) polymer, and/or (b) with an amorphous polymer (which may be an elastomer), e.g. a known PSA. In this aspect, the invention includes also PSA composites comprising a backing having a coating thereon of such a composition, particularly PSA-coated articles for use in the medical field, for example an assembly which comprises

( 1 ) a flexible backing,

(2) a solvent-free layer of a pressure-sensitive adhesive (PSA) which is secured to the backing, and which comprises a TPE or is at least partially covered by a layer comprising a TPE, said TPE comprising polymeric molecules which comprise (i) polymeric A blocks which

(a) are crystalline and have a melting point Tq, or

(b) are amorphous and have a glass transition point T _g h;

(ii) at least one polymeric B block which is linked to at least two A blocks and which

(a) is crystalline and has a melting point T _ms which is less than

(T _q -10)°C or less than (T _gh -10)°C or (b) is amorphous and has a glass transition point T _gs which is less than (T _q -10)°C or less than (Tg _h -10) ^o C.

wherein at least one block selected from the A and B blocks comprises a side chain comprising crystallizable moieties which render the block crystalline. . This aspect of the invention also includes processes for preparing assemblies by joining articles together using such a composition; and processes for disassembling such assemblies which include heating the PSA to weaken it. These PSA's, PSA composites, assemblies, and processes preferably have the functional characteristics set out in the earlier International Patent Application No. PCT/US92/01153, Publication No. WO 92/13901 referred to above to which reference should be made for details of this aspect of the invention. Reference should also be made to that publication for amorphous base resins, crystalline polymer additives, methods of formulating

PSA's, methods of applying PSA's to backings, backings, and methods of using PSA composites, which are generally suitable for use in this aspect of the invention.

In a seventh aspect, this invention provides a film or other article which comprises a TPE in which the A blocks, or the B blocks, or both, are SCC blocks, particularly an article which is suitable for use as a component of a food package and/or in a method which requires heat-sealing the film These films preferably have the functional characteristics set out in our earlier International Application No. PCT US91/09218 filed December 6, 1991, which also discloses food packages, and methods of packaging and storing foodstuffs, suitable for use in this aspect of the invention, and to which reference should be made for further details of this aspect of the invention. One assembly according to this aspect of the invention comprises

(1) a first film which comprises a TPE as defined in paragraph (2) above of the sixth aspect of the invention, and (2) a second film which is heat-sealed to the first film and which is composed of a polymeric composition which is compatible with the A block, or the B block, or both, of the TPE.

In an eighth aspect, this invention provides a hot melt adhesive comprising a TPE in which the A blocks, or the B blocks, or both, are SCC blocks and processes for joining two articles together which comprise forming a layer of a molten polymeric composition containing such a TPE between the articles, pushing the articles together, and allowing the composition to cool. Preferably the composition comprises a TPE as defined in paragraph (2) of the sixth aspect of the invention.

In a ninth aspect, this invention provides a composition which comprises

( 1 ) a TPE as defined in paragraph (2) of the sixth aspect of the invention, and

(2) intimately mixed with the TPE, a crystalline polymeric additive which (a) has a first order transition point T _a in the composition of 23° to

120°C, and (b) has a heat of fusion of at least 5 Joules/g.

DETAILED DESCRIPTION OF THE INVENTION

For clarity and convenience, the following detailed description of the invention is divided into various headings and sub-headings, e.g. by reference to the various different aspects of the invention. It is to be understood, however, that where a particular feature is discussed only under one heading, e.g. in relation to one aspect of the invention, that feature is applicable to the invention generally, and can for example be used in other aspects of the invention.

Definitions. Abbreviations and Measurements

In this specification, parts, amounts and percentages are by weight. Temperatures are in °C. Molecular weights are in Daltons and are determined by gel permeation chromatography (GPC) in THF (tetrahydrofuran) against a polystyrene standard, the M _n values being number average molecular weights and the M _w values being weight average molecular weights. In some places, M _w values are given in thousands, abbreviated as "k"; thus an M _w given as 65k means that the weight average molecular weight is 65,000 Daltons. First order transition points (often referred to as melting points), glass transition points, and heats of fusion (ΔF) are determined by a differential scanning calorimeter (DSC), using the second heat cycle and a heating rate of 10°C minute. The peak of the DSC curve is T _q when the measurement is carried out on the TPE, and T _m when the measurement is carried out on the hard block precursor before it is incorporated into the TPE. Glass transition points are taken at the mid-point (first derivative) of the secondary transition. Elongation (El) and tensile strength (TS) values are measured at 25°C using a tensile test instrument, for example an Instron tensile tester, at a crosshead speed of 0.5 inch/minute (1.27 cm/minute). Modulus values are Young's Modulus (YM) values measured in the same way as the elongation values. Viscosity values are measured at 25°C and a solids content of 30% (we used a Brookfield Viscometer Model LVT) and expressed in centipoise.

The term Cn is used herein to denote a linear compound or group containing n carbon atoms, and the abbreviations CnA, CnMA and CnlEMA are used to denote linear alkyl acrylates, linear alkyl methacrylates, and linear alkyl oxycarbonylamido- ethylmethacrylates in which the alkyl group contain n carbon atoms. For example, C4A is butyl acrylate, C16A is hexadecyl acrylate, and C22MA is docosanyl (also known as

behenyl) methacrylate. The abbreviations EHA, HEA, MBA and AA are used for 2- ethylhexyl acrylate, 2-hydroxyethyl acrylate, 3-methoxybutyl acrylate, and acrylic acid, respectively. The abbreviation AIBN is used for azo bis-isobutyronitrile. The abbreviation IEMA is used for isocyanatoethylmethacrylate.

Shear and Tack Values are measured by Test Procedures PSTC-7 and PSTC-6, respectively, of the Pressure-Sensitive Tape Council. In the Shear Test, a sample of the PSA composite 0.5 inch (1.25 cm) square is pressed against a vertical steel plate, and after 5 minutes, a 1000 g weight is secured to the backing; the shear value is the time in seconds before the backing falls off the plate. In the Tack Test, a ball bearing 7/16 inch (1.1 cm) in diameter is allowed to roll down a standard incline onto the PSA surface of the composite; the tack value is the distance in cms that the ball runs over the PSA.

Peel Strengths for PSA composites applied to human skin are measured as follows. After removing the release sheet (if any), two identical samples are placed on the underside of the forearm of an adult, with the length of the strips parallel to the arm bone. Light hand pressure is applied to the entire surface of the strips. After about 0.5 hour, 1 hour, 24 hours, or 48 hours, one end of one strip is detached from the skin and attached to a clip which is attached by a wire to the load cell of an Instron Materials Testing Instrument (IMTI) or an equivalent instrument. The sample is then removed by peeling it off at a rate of 10 inch (25.4 cm) per minute, the sample being bent back over itself at an angle of about 180°. The other strip is removed in the same way, except that a hair dryer is used to warm the entire strip to a temperature of about 40°C before it is peeled off. The average peel strength for each strip is recorded at room temperature (LT) and at the higher temperature (HT).

Moisture Vapor Transmission Rates (MVTR) are measured by ASTM E96-60, using the desiccant method, at 37°C and a humidity difference of about 70%, and are expressed in g/mil/m ² /24 hr.

SCC Blocks

The earlier International Application PCT/US92/08508 (Publication No. 93/07194) contains a full disclosure of SCC blocks which may be present as hard blocks in the TPE's of that application. That disclosure is generally applicable to the SCC blocks which may be used as hard or soft blocks in the various aspects of this invention, subject of course to the

requirement that an SCC block which is a soft block must have a melting point less than the T _g or T _m of the hard block. The following description can therefore be supplemented by reference to the disclosure in that earlier apphcation. When the SCC block melts, the difference between the onset of melting (T ₀ ) and the peak (Tq or T _ms ) on a DSC curve is preferably less than 10°C, more preferably less than 8°C, particularly less than 6°C, especially less than 4°C. The melting point of the SCC block on its own, T _m , is closely related to T _q (in a hard block) or T _ms (in a soft block). T _q or T _ms will generally be between (T _m - 10)°C and (T _m + 5)°C, usually between (T _m - 5)°C and T _m . T _q and/or T _ms are generally 0° to 200°C, preferably less than 150°C, particularly less than 85°C. In the SCC blocks, preferably 50 to 100%, particularly 70 to 100%, especially 90 to 100%, of the repeating units contain crystallizable side chains. The ΔF of the SCC block on its own is generally at least 5 or at least 10, preferably at least 20, particularly at least 40, for example 60 to 120, Joules/g.

The SCC blocks can be broadly defined as polymer blocks which comprise

-Y- repeating units of the general formula I where Y is an organic radical forming part of the

Cy polymer backbone and Cy comprises a crystallizable moiety. The radical Cy may be aliphatic or aromatic, for example alkyl of at least 10 carbons, fluoralkyl of at least 6 carbons or p-alkyl styrene wherein the alkyl contains 6 to 24 carbons. Preferred SCC blocks comprise side chains containing in total at least 5 times as many carbon atoms as the backbone of the block, particularly side chains comprising linear polymethylene moieties containing 12 to 50, especially 14 to 22, carbon atoms, or linear perfluorinated or substantially perfluorinated polymethylene moieties containing 6 to 50 carbon atoms. The blocks can optionally also contain units derived from one or more other comonomers generally in total amount less than 50%, particularly less than 35%, especially less than 25%, e.g. 0 to 15%.

Other precursors of SCC blocks, and SCC blocks which can be formed by a living polymerization on another preformed block, include atactic and isotactic polymers of n- alkyl α-olefins, n-alkylglycidyl ethers, n-alkyl vinyl ethers, n-alkyl-α-epoxides, n-alkyl oxycarbonylamido-ethylmethacrylates, n-fluoro alkyl acrylates, n-alkyloxazolines , and polymers obtained by reacting an hydroxyalkyl acrylate or methacrylate with an alkyl

isocyanate, or by reacting a difunctional isocyanate, a hydroxyalkyl acrylate or methacrylate, and a primary fatty alcohol.

Preferred SCC blocks comprise 60 to 100% of units derived from at least one monomer selected from the group consisting of alkyl acrylates, alkyl methacrylates, N-alkyl acrylamides, N-alkyl methacrylamides, alkyl oxazolines, alkyl vinyl ethers, alkyl vinyl esters, α-olefins, alkyl 1,2-epoxides and alkyl glycidyl ethers in which the alkyl groups are n-alkyl groups containing 14 to 50 carbon atoms, and the corresponding fluoroalkyl monomers in which the alkyl groups are n-alkyl groups containing 6 to 50 carbon atoms; 0 to 20% of units derived from at least one monomer selected from the group consisting of alkyl acrylates, alkyl methacrylates, N-alkyl acrylamides, alkyl vinyl ethers, and alkyl vinyl esters in which the alkyl groups are n-alkyl groups containing 4 to 12 carbon atoms; and 0 to 15% of units derived from at least one polar monomer selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, acrylamide, methacrylamide, acrylonitrile, ethacrylonitrile, vinyl acetate and N vinyl pyrrolidone. Such SCC block polymers may also contain units derived from other monomers to change compatibility with other blocks, or to raise the modulus of the TPE; such monomers include styrene, vinyl acetate, monoacrylic functional polystyrene and the like.

The number average molecular weight of the SCC block is preferably less than

200,000, more preferably less than 100,000, particularly less than 50,000, more particularly 2,000 to 20,000, especially 3,000 to 20,000.

When a TPE used in this invention includes hard SCC blocks, preferably all the hard blocks in the TPE are SCC blocks. The hard SCC blocks are preferably all of the same type, with each block being derived from the same monomer or mixture of monomers. When two different SCC hard blocks are present, the TPE may have two or more distinct Tq's, corresponding to the different SCC blocks. When conventional hard blocks are also present, they preferably do not amount to more than 10%, particularly not more than 5%, of the TPE. Such other hard blocks, if present, can be of any kind, including those disclosed in the documents incorporated by reference herein.

When the TPE's include non-SCC soft (B) blocks, the soft blocks can be of any kind, including those disclosed in the documents incorporated by reference herein. The

TPE can contain one or more different types of non-SCC B blocks. The glass transition point (Tgs) or melting point (T _ms ) of the B blocks should be below (T _q - 10)°C, preferably less than (T _q - 20)°C, particularly less than (T _q - 40)°C. T _gs or T _ms should also be below the temperature at which the TPE should exhibit elastomeric properties in use, for example less than 20°C, preferably less than 0°C, particularly less than -20°C, e.g. less than -40°C.

When the TPE contains more than one non-SCC B block, the B blocks will usually be the same; however, the TPE can contain two or more different B blocks. A B block can contain a single repeating unit (which may be derived from a single monomer or a pair of monomers) or two or more different repeating units. When there are two or more different repeating units in a B block, they can be distributed randomly or in blocks.

Examples of suitable amorphous B blocks are polyethers, polyacrylates, polyesters, polyamides, polyurethanes, and polysiloxanes.

The linkages between repeating units in a B block can be the same as, or different from, the linkages between repeating units in the SCC A blocks. The linkages between the

B block(s) and the A blocks can be the same as, or different from, the linkages between repeating units in the B block(s). They can for example be the residue of a linking compound which contains at least two reactive groups which will react with groups on the

A and B blocks, for example a diisocyanate such as methylene diphenylene diisocyanate, tolylene diisocyanate, or hexamethylene diisocyanate.

The number average molecular weight of the B blocks is generally more than 5,000 and less than 900,000, preferably less than 500,000, particularly less than 200,000, especially less than 100,000, e.g. 10,000 to 80,000.

When the TPE includes soft SCC blocks, preferably all the soft blocks in the TPE are SCC blocks. The soft SCC blocks are preferably all of the same type, with each block being derived from the same monomer or mixture of monomers. When two different SCC soft blocks are present, the TPE may have two or more distinct T _ms 's, corresponding to the different SCC blocks. When conventional soft blocks are also present, they preferably do not amount to more than 10%, particularly not more than 5%, of the TPE. Such other soft blocks, if present, can be of any kind, including those disclosed in the documents incorporated by reference herein.

As indicated above, T _m s will be selected according to the intended use of the TPE. Thus Tms ^an be selected so that the TPE changes, over a predetermined and relatively narrow temperature range including T _ms , between a relatively hard and inflexible material and an elastomeric material. For most uses, T _m s is preferably less than 60°C, particularly less than 45°C, especially less than 30°C. T _ms is also preferably more than 0°C, particularly more than 5°C. For example, T _ms may be 3° to 40°C, preferably 5° to 20°C. In one preferred embodiment, the B block is a polyacrylate, preferably a polyacrylate which contains 50 to 100%, preferably 80 to 100%, of units derived from at least one n-alkyl acrylate or methacrylate in which the alkyl group contains 4 to 16, particularly 12 to 14, carbon atoms or from an equivalent monomer, e.g. an acrylamide or methacrylamide. Such B blocks may for example include units derived from one or more other ethylenically unsaturated comonomers including AA, EHA, HEA, MBA and methacrylic acid.

When the TPE includes non-SCC hard (A) blocks, the detailed description given above for non-SCC soft (B) blocks is generally applicable, subject only to the limitation that the melting point (T h) or glass transition point (T _g h) of the block must be higher, rather than lower, than the melting point of the SCC block T _ms ). Thus T _ms should be below (Tmh-10)°C or (T _g h-10)°C, preferably below (T _m h-20)°C or (Tg _h -20) ^o C, particularly below (Tmh- 0)°C or (T _gh -40) ^o C.

When a TPE used in the invention contains SCC hard (A) blocks, each soft (B) block must be linked to at least two SCC A blocks having a T _q higher than the T _gs or T _ms of the B block. The A blocks are insoluble in the B block(s) when the TPE is solid, and therefore anchor the B block(s) at temperatures below Tq, thus providing elastomeric properties below Tq and above T _gs or T s- However the crystallizable side chains in the novel A blocks apparently plasticize the TPE at temperatures above T _q and thus assist in the very rapid reduction in viscosity at temperatures just above Tq. The greater the compatibility of the A and B blocks above T _q , the larger the reduction in viscosity. The complex viscosity of the TPE preferably decreases from a first value Qi dynes/cm ² to a second value Q2 dynes/cm ² , where Q2 is less than Qi x 10 ^-3 , preferably less than Qi x 10" ⁵ , as the temperature increases from Ti to T2, where Ti is less than T _q , e.g. (T _q - 3)°C, (T _q - 5)°C or (T _q - 10)°C and T ₂ is at most (T _q + 10)°C, e.g. (Tq + 7)°C or (T _q + 4)°C. The

TPE exhibits a corresponding decrease in complex modulus over the same temperature range.

When the soft block is crystalline, preferably T _q is 40 to 125°C and T _m s is 3 to 40°C. In one preferred TPE, the B block comprises 50 to 100%, preferably 75 to 100%, by weight of units derivable from at least one n-alkyl acrylate or methacrylate in which the n-alkyl group contains 4 to 16 carbon atoms, preferably C12A or C14A or both, and the A block comprises 50 to 100%, preferably 75 to 100%, by weight of units derivable from at least one n-alkyl acrylate or methacrylate in which the n-alkyl group contains at least 18 carbon atoms, preferably 18-30 carbon atoms, particularly from C22A.

The TPE's generally have an ABA (triblock), (AB) _n , or A _n B structure where n is at least 2, though mixtures of such structures can be used. The A _n B structure includes the various different types of graft copolymer which can be prepared. The TPE's will generally contain 2 to 90% of the SCC blocks. TPE's to be used in PSA's preferably contain 2 to 15%, particularly 3 to 10%, of the SCC hard blocks. TPE's for other uses can contain for example 10 to 90%, preferably 10 to 70%, particularly 25 to 60%, of the SCC hard blocks. The crystallizable moieties in the SCC hard blocks may provide less than 65%, particularly less than 60%, of the TPE.

The TPE's used in this invention generally exhibit elongations of 5 to 500%, e.g. 50 to 500%. Their modulus is generally 10 to 100,000 psi (0.7 to 7,000 kg/cm ² ), e.g. 10 to 50,000 psi (0.7 to 3500 kg/cm ² ). The higher the proportion of hard blocks, the higher the modulus. The TPE's generally contain less than 90%, preferably less than 70%, and more than 2% of the hard blocks.

The number average molecular weight (M _n ) of the TPE's used in this invention is generally 5,000 to 800,000, preferably 10,000 to 800,000, for example 5,000 to 400,000, particularly 10,000 to 200,000. The ratio M _w /M _n is generally from 1 to 15, e.g. 2 to 4.

The TPE's used in this invention can be prepared by the methods which are described in detail in the earlier International Application No. PCT/US92/08508, Publication No. WO 93/07194 (Docket No. 9213.1 PCT), to which reference should be made for details of this aspect of the invention.

Compositions. Shaped Articles and Assemblies

In the compositions, shaped articles, and assemblies of the invention, a TPE containing SCC hard blocks and crystalline soft blocks is associated with a second component which contacts the TPE. These compositions, shaped articles and assemblies (including their preparation, their use, and their advantages) can be substantially the same as the corresponding compositions, shaped arf tides and assemblies which contain SCC hard blocks and amorphous soft blocks, and which are described in detail in the earlier International Application No. PCT/US92/08508, Publication No. WO93/07194 (Docket No. 9213.1 PCT), to which reference should be made for details of this aspect of the invention.

The invention is illustrated in the following Examples.

EXAMPLES

In Examples 1 to 14, the first step was to make a hard block SCC acrylate and/or methacrylate polymer, using the ingredients and amounts thereof (in grams) shown in Table 1 to make one of the SCC polymers HI to H4 having the properties shown in Table 1. The SCC polymer was then functionalized by reaction with isocyanatoethylmethacrylate (IEMA).

Preparation of Hard Block SCC Polymers HI to H4

SCC polymer HI was prepared by adding the C16A (400 g), C18A (100 g), mercaptoethanol (5.2 g) as capping agent, and AIBN (1 g) as initiator, to toluene (1000 mL), and heating the reaction mixture with reflux and stirring under nitrogen first at 60°C for 16 hours and then at 80°C for 6 hours. The SCC polymer was then functionalized by heating with IEMA (10 g) and dibutyl tin dilaurate (7 drops) at 60°C for 16 hours. SCC polymers H2 to H4 were made similarly..

Preparation of the TPE's

In Examples 1-8, the HI functionalized SCC polymer, EHA and HEA, in the amounts shown in Table 4, were added to a reaction vessel, together with ethyl acetate (100 g), heptane (100 g) and AIBN (0.15 g), and heated at 60°C for 16 hours under nitrogen. The reaction mixture was cooled and poured into ethanol to recover the TPE as a precipitate, and the

precipitate was dried at elevated temperature under reduced pressure. In Examples 9-14, the TPE was made similarly, using the ingredients and amounts thereof shown in Table 4. In Example 11, the TPE, which contained 20% of H2, had a crystalline soft block with a T _m s of about 6°C (and onset of melting at 2°C) resulting from the C12A and C14A units and a crystalline hard block with a Tq of about 61°C (and onset of melting at about 54°C) resulting from the H2 (C22A) macromer.

Preparation of Copolvmers C1-C13

Copolymers C1-C13 are random high molecular weight acrylate polymers. Typically they were prepared by adding the monomers and amounts thereof in Table 3 to a reaction vessel, together with ethyl acetate (100 g), heptane (100 g) and AIBN (0.15 g) and heating the reaction mixture at 60°C for 16 hours under nitrogen. The copolymer was recovered by pouring the cooled reaction mixture into ethanol and drying the precipitate at elevated temperature under reduced pressure.

Preparation of Copolvmers WOC1. WOC2 and WOC3

Copolymers WOC1, WOC2 and WOC are low molecular weight random SCC polymers which can be added to PSA's to reduce peel strength on warming. They were prepared in the same general way as C1-C13, using the monomers and amounts thereof shown in Table 4, but taking steps to control the molecular weight.

Preparation and Testing of PSA's

A number of PSA composites were made and tested, as summarized in Table 5 below. Table 5 shows the results for PSA composites in which the PSA comprises a TPE containing SCC hard blocks. A number of the PSA's also contained one of the crystalline SCC additives ("cryst. SCC") WOC1, WOC2 or WOC3. Table 6, which is included for comparison, shows results for comparable PSA's which do not include such SCC hard blocks. Table 7 shows the results of testing on human skin.

Except for PSA composite No. QA141, the PSA composites were made and tested as follows. The specified polymer(s) was dissolved in a suitable solvent, e.g. toluene or heptane, to give a homogeneous, bubble-free composition with a solids content of about 45%. The composition was applied to a polyester TPE ("Hytrel 4056") film 1.75 mil (0.0045 cm) thick,

in the following way. The film was secured to a flat glass plate 18 x 12 inch (46 x 30.5 cm) and smoothed to remove air bubbles between the film and the plate. A wire-wound applicator rod (No. 70 Gardco Wet Film Applicator Rod) was then used to apply a coating of the composition to the film. The coating was dried in an oven at 90°C for 30 minutes or more. The dried coating thickness was about 1.6 to 1.8 mil (0.0040 to 0.0046 cm). The coating was covered with a siliconized polyethylene-impregnated paper. The resulting laminate was removed from the glass plate and samples about 4.0 x 0.5 inch (10 x 1.25 cm) were cut from the laminate.

PSA composite QA 141 was made by coating PSA QA 112 by the method described above to give a coating 1 mil thick. This coating was then covered by a coating about 3 microns thick of PSA QA 111 , by transfer coating from a siliconized Mylar film.

The PSA composites were tested as previously described.

Preparation and Heat Sealing of Films of TPE's

The TPE of Example 11 was formed into a film as follows. The polymer (10 g) was dissolved in a mixture of toluene (12.5 mL) and heptane (12.5 mL), coated onto a siliconized polyester backing and dried at 90°C. The dried film was transferred to a microporous support (Cellgard K878). The random copolymer C13 was formed into a film in the same way. The Example 11 film could readily be heat-sealed to a commercially available film of a blend of polyethylene (PE) and ethylene/vinyl acetate copolymer (EVA). The copolymer C13 film gave a markedly inferior heat seal. The oxygen permeabilities of the Example 11 film and the PE/EVA film were measured and are shown below (in cc-ml/100in ² -atm-24 hrs).

at45°F at72°F

Example 11 1800 5150

PE/EVA 270 650

+ In Examples 9 and 10, the soft block monomers also included 5 g MPEG (Example 9) or 25 g MBA (Example 10)

++ In Example 11, the soft block was formed from C12A, C14A and AA (50/47/3)

TABLE 3

C9 had a viscosity of 3000 cps. CIO had a viscosity of 400 cps.

TABLE 4

Copolymer Ingredients M _w M _w /M _n

C16A C18A AA

WOC1 54.1 40.9 5.0 2.5k 1.48

WOC2 54.1 40.9 5.0 3.7k 1.5

WOC3 95 - 5 2k 1.57

TABLE 5

TABLE 5. continued

TABLE 6

TABLE 6 (continued)

TABLE 7

Peel Strengths of PSA's on Human Skin

PSA Adhesive

QA67 OB71 OB81 OA92 QA93 OB91 OA101 OB 121 OA141

After 0.5 hr, at LT - 60 - - - - - - - at HT - 6 - - - - - - -

% reduction - 90% - - - - - - -

After l hr, at LT 29 - 23.8 14 40 55 43 44 26 at HT 3 - 3.4 2 5.5 2.5 - - 2.1

% reduction 89% - 86% 85% 26% 95% - - 92%

After 24 hr, atLT 80 211 89 - 95 - 79.5 78 - atHT 9.5 21 29 - 9 . - - -

% reduction 88% 90% 67% - 91% . - - -

After 48 hr, atLT 90 - 89 . - - _ _ - atHT 12 - 38 - - - - - -

% reduction 87% - 57 - - - - - -

Sheer Strength 139k 17 312 >86k 717 77 1655 600 1906