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A polypropylene-based calendered or injection-molded article satisfying the requirements of (1) having a tensile modulus TM of 5 MPa or higher and (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: TM≧5×Tm&

A polypropylene-based calendered or injection-molded article satisfying the requirements of (1) having a tensile modulus TM of 5 MPa or higher and (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: TM≧5×Tm−450, is less tacky and excellent in flexibility and transparency. Such a polypropylene-based calendered or injection-molded article is produced from a propylene polymer satisfying the requirements of (1) having a component soluble in a 25° C. hexane in a content H25 of 0 to 80% by weight; (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: &Dgr;H≧6×(Tm−140) wherein &Dgr;H is a melting endotherm (J/g); and (3) having an intrinsic viscosity [η] of 1 to 3 dl/g as measured at 135° C. in tetralin.

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A polypropylene-based calendered or injection-molded article satisfying the requirements of (1) having a tensile modulus TM of 5 MPa or higher and (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: TM≧5×Tm&

A polypropylene-based calendered or injection-molded article satisfying the requirements of (1) having a tensile modulus TM of 5 MPa or higher and (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: TM≧5×Tm−450, is less tacky and excellent in flexibility and transparency. Such a polypropylene-based calendered or injection-molded article is produced from a propylene polymer satisfying the requirements of (1) having a component soluble in a 25° C. hexane in a content H25 of 0 to 80% by weight; (2) having, when measured by a differential scanning calorimeter (DSC), no melting point or a melting point Tm (° C.) satisfying the formula: &Dgr;H≧6×(Tm−140) wherein &Dgr;H is a melting endotherm (J/g); and (3) having an intrinsic viscosity [η] of 1 to 3 dl/g as measured at 135° C. in tetralin. e, cobalt (II) bromide, nickel (II) bromide, antimony (III) bromide, and palladium (II) bromide.10. The bonding composition of claim 1, wherein the metal salt is present in an amount greater than 0 ppm and less than about 40,000 ppm based on the bonding composition.11. The bonding composition of claim 1, wherein the metal salt is present in the bonding composition in an amount ranging from about 60 ppm to about 20,000 ppm based on the bonding composition.12. The bonding composition of claim 1, wherein the metal salt is present in the bonding composition in an amount ranging from about 100 ppm to about 4,000 ppm based on the bonding composition.13. The bonding composition of claim 1, wherein the bonding composition comprises about 0.003 to about 1.5%-wt. boron in the form of an organoborane, and less than about 40,000 ppm metal salt based on the bonding composition.14. The bonding composition of claim 1, wherein the organoborane is complexed with a complexing agent and wherein the bonding composition further includes a decomplexer.15. The bonding composition of claim 14, wherein the complexing agent is selected from the group consisting of amines, amidines, hydroxides, alkoxides, and combinations thereof.16. The bonding composition of claim 14, wherein the decomplexer is selected from the group consisting of acid, anhydride, aldehyde, ß-ketone compound, isocyanate, acid chloride, sulfonyl chloride, and combinations thereof.17. The bonding composition of claim 1, wherein the at least one polymerizable monomer is selected from the group consisting of (meth)acrylates, (meth)acrylamides, and mixtures thereof.18. The bonding composition of claim 1, wherein the at least one polymerizable monomer is selected from the group consisting (meth)acrylic esters of monohydric alcohols and (meth)acrylic acid esters of polyhydric alcohols.19. The bonding composition of claim 1 further including a reactive diluent.20. The bonding composition of claim 1, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 5 minutes or greater.21. The bonding composition of claim 1, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 10 minutes or greater.22. The bonding composition of claim 1, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 20 minutes or greater.23. A bonded composite comprising a first substrate; and a second substrate adhesively bonded together by a layer of a cured bonding composition according to claim 1.24. The bonded composite of claim 23, wherein at least one of the first and second substrates is a low surface energy polymeric material.25. The bonded composite of claim 23, wherein the first and second substrates are each independently selected from low surface energy polymeric materials.26. The bonded composite of claim 23, wherein at least one of the first and second substrates is selected from the group consisting of polyethylene, polypropylene and polytetrafluoroethylene.27. The bonded composite of claim 26, wherein the first and second substrates are each independently selected from the group consisting of polyethylene, polypropylene and polytetrafluoroethylene.28. A reactive, two-part bonding composition comprising: (a) an initiator component comprising an organoborane; and (b) a polymerizable composition comprising: at least one polymerizable monomer; anda metal salt according to formula (1):[M a+Ln][X−m]a/m  (1) wherein:M is a metal cation having two chemically accessible oxidation states and having positive charge a, where a is an integer ranging from 1 to 6;X is a counterion having charge −m, where m is an integer ranging from 1 to 3;L is a covalently bonded ligand; andn is an integer ranging from 0 to 10 representing the number of ligands covalently bonded to the metal cation.29. The reactive two-part bonding composition of claim 28, wherein the first part and th e second part are combined in a whole number ratio of about 1:10 to about 1:1.30. The reactive two-part bonding composition of claim 28, wherein the organoborane is complexed with a complexing agent and wherein the second part further comprises a decomplexer.31. The reactive two-part bonding composition of claim 28, wherein M is a cation selected from the group consisting of vanadium, chromium, manganese, iron, cobalt, nickel, copper, molybdenum, ruthenium, rhodium, palladium, antimony, platinum, and cerium.32. The reactive two-part bonding composition of claim 28, wherein M is a cation selected from the group consisting of manganese, iron, cobalt, and copper.33. The reactive two-part bonding composition of claim 28, wherein M is a copper or iron cation.34. The reactive two-part bonding composition of claim 28, wherein the two chemically accessible oxidation states of metal cation M are separated by one unit of charge.35. The reactive two-part bonding composition of claim 28, wherein X is selected from the group consisting of halides, borates, sulfonates, and carboxylates.36. The reactive two-part bonding composition of claim 28, wherein X is selected from the group consisting of chloride, bromide, tetrafluoroborate, trifluoromethanesulfonate, naphthenate, and 2-ethylhexanoate.37. The reactive two-part bonding composition of claim 28, wherein L is selected from the group consisting of water, ammonia, amine, carbonyl, isonitriles, phosphines, phosphites, arsines, nitrosyl, ethylene and alkenes.38. The reactive two-part bonding composition of claim 28, wherein the metal salt is selected from the group consisting of copper (II) bromide, copper (II) chloride, copper (II) 2-ethylhexanoate, iron (III) bromide, vanadium (III) bromide, chromium (III) bromide, ruthenium (III) bromide, copper (II) tetrafluoroborate, copper (II) trifluoromethanesulfonate, copper (II) naphthenate, copper (I) bromide, iron (III) bromide, manganese (II) bromide, cobalt (II) bromide, nickel (II) bromide, antimony (III) bromide, and palladium (II) bromide.39. The reactive two-part bonding composition of claim 28, wherein the metal salt is present in an amount greater than 0 ppm and less than about 40,000 ppm based on the bonding composition.40. The reactive two-part bonding composition of claim 28, wherein the bonding composition comprises about 0.003 to about 1.5%-wt. boron in the form of an organoborane, and less than about 40,000 ppm metal salt based on the bonding composition.41. The reactive two-part bonding composition of claim 28, wherein the at least one polymerizable monomer is selected from the group consisting of (meth)acrylates, (meth)acrylamides, and mixtures thereof.42. The reactive two-part bonding composition of claim 28, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 5 minutes or greater.43. The reactive two-part bonding composition of claim 28, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 10 minutes or greater.44. The reactive two-part bonding composition of claim 28, wherein the bonding composition has a worklife as defined in the Worklife Test Method of about 20 minutes or greater.45. A reactive, two-part bonding composition comprising: (a) an initiator component comprising an organoborane and a metal salt according to formula (1): [M a+Ln][X−m]a/m  (1) wherein: M is a metal cation having two chemically accessible oxidation states and having positive charge a, where a is an integer ranging from 1 to 6; X is a counterion having charge -m, where m is an integer ranging from 1 to 3; L is a covalently bonded ligand; and n is an integer ranging from 0 to 10 representing the number of ligands covalently bonded to the metal cation; and (b) a polymerizable composition comprising at least one polymerizable monomer. 46. The reactive two-part bonding composition of claim 45, wherein the organoborane is complexed with a