A polyolefin composition made from or containing:

T1) 50-90 wt % of a recycled polyolefin mixture and
T2) 10-50 wt % of a polyolefin component, containing
A) 5-35% by weight of a propylene homopolymer or a propylene ethylene copolymer;
B) 20-50% by weight of an ethylene homopolymer; and
C) 30-60% by weight of a terpolymer of ethylene, propylene, and 1-butene made from or containing 45 to 65 percent by weight of ethylene units and from 15 to 38 percent by weight of 1-butene units.

Disclosed is a polypropylene with an MFR of at least 20 g/10 min comprising a homopolypropylene and optionally within a range from 2 wt % to 30 wt % of an propylene-α-olefin copolymer by weight of the polypropylene; wherein the homopolypropylene has a MFR within a range from 30 g/10 min to 200 g/10 min, an Mw/Mn within a range from 7 to 16, and comprising 1.1 wt % or less atactic polypropylene based on the total weight of the homopolypropylene and atactic polypropylene, where the propylene-α-olefin copolymer has within a range from 30 wt % to 50 wt % α-olefin derived units by weight of the propylene-α-olefin copolymer, and an intrinsic viscosity within a range from 4 to 8 dL/g. The impact copolymer may be obtained by combining a Ziegler-Natta catalyst having at least two different internal electron donors with propylene in reactors in series to produce the homopolypropylene followed by a gas phase reactor to produce a propylene-α-olefin copolymer.

Disclosed is a polypropylene with an MFR of at least 20 g/10 min comprising a homopolypropylene and optionally within a range from 2 wt % to 30 wt % of an propylene-α-olefin copolymer by weight of the polypropylene; wherein the homopolypropylene has a MFR within a range from 30 g/10 min to 200 g/10 min, an Mw/Mn within a range from 7 to 16, and comprising 1.1 wt % or less atactic polypropylene based on the total weight of the homopolypropylene and atactic polypropylene, where the propylene-α-olefin copolymer has within a range from 30 wt % to 50 wt % α-olefin derived units by weight of the propylene-α-olefin copolymer, and an intrinsic viscosity within a range from 4 to 8 dL/g. The impact copolymer may be obtained by combining a Ziegler-Natta catalyst having at least two different internal electron donors with propylene in reactors in series to produce the homopolypropylene followed by a gas phase reactor to produce a propylene-α-olefin copolymer.

A process for the preparation of a propylene polymer containing a coloring agent, including the steps of:

(i) forming a solid mixture (a-b)of (a) a ZN catalyst component made from or containing Mg, Ti, halogen and an internal electron donor compound, and (b) a coloring agent made from or containing at least a pigment; wherein the mixture being in a weight ratio (b):(a) ranging from 0.01:1 to 0.4:1; and

(ii) feeding the mixture (a-b) to a polymerization reactor and operating the reactor under polymerization conditions to produce the propylene polymer.

wherein the process having the b:a weight ratio and a time in days elapsed between mixture formation and use in polymerization fall below the curve defined by the equation y=3+0.832x.sup.−1,17 wherein y is the time in days elapsed between mixture formation and use in polymerization and x is the (b):(a) weight ratio.

A process for the preparation of a propylene polymer containing a coloring agent, including the steps of:

(i) forming a solid mixture (a-b)of (a) a ZN catalyst component made from or containing Mg, Ti, halogen and an internal electron donor compound, and (b) a coloring agent made from or containing at least a pigment; wherein the mixture being in a weight ratio (b):(a) ranging from 0.01:1 to 0.4:1; and

(ii) feeding the mixture (a-b) to a polymerization reactor and operating the reactor under polymerization conditions to produce the propylene polymer.

wherein the process having the b:a weight ratio and a time in days elapsed between mixture formation and use in polymerization fall below the curve defined by the equation y=3+0.832x.sup.−1,17 wherein y is the time in days elapsed between mixture formation and use in polymerization and x is the (b):(a) weight ratio.

A solid catalyst component for the polymerization of olefins CH.sub.2═CHR in which R is hydrogen or a hydrocarbon radical with 1-12 carbon atoms, made from or containing Mg, Ti, Bi, halogen and an electron donor obtained from a process including the steps: (a) dissolving a Mg(OR).sub.2 compound wherein R groups, equal to or different from each other, are C.sub.1-C.sub.15 hydrocarbon groups optionally containing a heteroatom selected from O, N and halogen, in an organic liquid medium, thereby forming a first liquid mixture; (b) contacting the first liquid mixture (a) with TiCl.sub.4, thereby forming a second liquid mixture absent a solid phase, and (c) subjecting the second liquid mixture (b) to conditions, whereby solid catalyst particles are formed, wherein (i) a Bi compound and (ii) a bidentate electron donor compound are present in one or more of steps (a) to (c) and/or contacted with the solid catalyst particles obtained from (c).

A solid catalyst component for the polymerization of olefins CH.sub.2═CHR in which R is hydrogen or a hydrocarbon radical with 1-12 carbon atoms, made from or containing Mg, Ti, Bi, halogen and an electron donor obtained from a process including the steps: (a) dissolving a Mg(OR).sub.2 compound wherein R groups, equal to or different from each other, are C.sub.1-C.sub.15 hydrocarbon groups optionally containing a heteroatom selected from O, N and halogen, in an organic liquid medium, thereby forming a first liquid mixture; (b) contacting the first liquid mixture (a) with TiCl.sub.4, thereby forming a second liquid mixture absent a solid phase, and (c) subjecting the second liquid mixture (b) to conditions, whereby solid catalyst particles are formed, wherein (i) a Bi compound and (ii) a bidentate electron donor compound are present in one or more of steps (a) to (c) and/or contacted with the solid catalyst particles obtained from (c).

A polypropylene composition made from or containing: A) from 88.0 wt. % to 98.0 wt. %, of a random copolymer of propylene containing from 0.8 wt. % to 4.8 wt. % of 1-hexene derived units; the random copolymer of propylene having: a Melt Flow Rate: measured according to ISO 1133 (230° C., 5 Kg) ranging from 0.5 to 4.4 g/10 min; and B) from 2.0 wt. % to 12.0 wt. % of a terpolymer of propylene ethylene and 1-hexene having a content of ethylene derived units ranging from 35 wt. % to 60 wt.; and a content of 1-hexene derived units ranging from 1 wt. % to 6 wt. %; wherein the polypropylene composition has a Melt Flow Rate: measured according to ISO 1133 (230° C., 5 Kg) ranging from 0.5 to 5.0 g/10 min.

A polypropylene composition made from or containing: A) from 88.0 wt. % to 98.0 wt. %, of a random copolymer of propylene containing from 0.8 wt. % to 4.8 wt. % of 1-hexene derived units; the random copolymer of propylene having: a Melt Flow Rate: measured according to ISO 1133 (230° C., 5 Kg) ranging from 0.5 to 4.4 g/10 min; and B) from 2.0 wt. % to 12.0 wt. % of a terpolymer of propylene ethylene and 1-hexene having a content of ethylene derived units ranging from 35 wt. % to 60 wt.; and a content of 1-hexene derived units ranging from 1 wt. % to 6 wt. %; wherein the polypropylene composition has a Melt Flow Rate: measured according to ISO 1133 (230° C., 5 Kg) ranging from 0.5 to 5.0 g/10 min.

The present invention relates to a process for the continuous preparation of a polyolefin from one or more α-olefin monomers in a reactor system, the process for the continuous preparation of polyolefin comprising the steps of: +feeding a polymerization catalyst to a fluidized bed through an inlet for a polymerization catalyst; +feeding the one or more monomers to the reactor, +polymerizing the one or more monomers in the fluidized bed to prepare the polyolefin; +withdrawing polyolefin formed from the reactor through an outlet for polyolefin; +withdrawing fluids from the reactor through an outlet for fluids and transporting the fluids through first connection means, an heat exchanger to cool the fluids to produce a cooled recycle stream, and through second connection means back into the reactor via an inlet for the recycle stream; wherein a thermal run away reducing agent (TRRA) is added to the reactor in a discontinuous way.