Abstract: A polypropylene composition made from or containing: A) from 76 wt % to 95 wt % of a propylene homopolymer having: fraction soluble in xylene at 25° C. between 2.0 wt % and 4.5 wt %; and melt flow rate ranging from 60.0 to 110.0 g/10 min; and B) from 5 wt % to 24 wt % of a copolymer of propylene and ethylene containing from 75 wt % to 90.0 wt % of ethylene derived units; wherein the polypropylene composition has content of ethylene derived units in the fraction soluble in xylene at 25° C. lower than the content of ethylene derived units of component B) and ranging from 51.0 wt % to 74.0 wt %; and at least two melting points, wherein the higher melting points ranges from 156.0° C. to 166.0° C. and the lower melting point ranges from 90.0° C. to 125.0° C.; wherein the sum of the amounts of component A) and B) being 100 wt %.

Abstract: A polypropylene composition made from or containing: from 70 wt % to 90 wt % of a propylene 1-hexene copolymer containing from 1.0 wt % to 5.0 wt % of 1-hexene derived units and a polydispersity index (PI) between 9.2 and 21.3; and from 10 wt % to 30 wt % of a copolymer of propylene and ethylene containing from 45.0 wt % to 65.0 wt % of ethylene derived units; the sum A)+B) being 100.

Abstract: A propylene/1-hexene copolymer having i) the content of 1-hexene derived units, measured by C13-NMR, ranging from 1.5 wt % to 2.5 wt % and the content of propylene derived units ranging from 97.5 to 98.5 wt. %; ii) a melting temperature, measured by DSC, ranging from 148 to 153° C.; iii) an amount of fraction insoluble in xylene at 25° C. higher than 97.0%; and iv) a melt flow rate (MFR), measured according to ISO 1133, 230° C., 2.16 kg, ranging from 35 to 65 g/10 min.

Abstract: The present invention relates to MgCl2.(EtOH),m(ROH)n(H2O)p adduct in which R is a C1-C15 hydrocarbon group different from ethyl, n and m are indexes, higher than 0, satisfying the equations (n+m)?0.7 and 0.05?n/(n+m)?0.95 and p is a number ranging from 0 to 0.7 with the proviso that when R is methyl and (n+m) is in the range of 0.7 to 1, the value of n/(n+m) ranges from 0.05 to 0.45. The catalyst components obtained from the adducts of the present invention are capable to give catalysts for the polymerization of olefins characterized by enhanced activity with respect to the catalysts prepared from the adducts of the prior art.

Abstract: The present invention relates to MgCl2.(EtOH),m(ROH)n(H20)p adduct in which R is a C1-C15 hydrocarbon group different from ethyl, n and m are indexes, higher than 0, satisfying the equations (n+m)?0.7 and 0.05?n/(n+m)?0.95 and p is a number ranging from 0 to 0.7 with the proviso that when R is methyl and (n+m) is in the range of 0.7 to 1, the value of n/(n+m) ranges from 0.05 to 0.45. The catalyst components obtained from the adducts of the present invention are capable to give catalysts for the polymerization of olefins characterized by enhanced activity with respect to the catalysts prepared from the adducts of the prior art.

Abstract: A process for the preparation of alkylidene substituted succinates comprising a step (a) in which is carried out the reaction of a carbonilic compound, a succinic and a base in a reaction medium and a step (b) in which the alkylidene substituted product obtained in (a) is esterified, characterized in that the succinic ester is used in a molar amount substantially equal to, or lower than, the amount of compound carbonilic compound, (ii) the base is used in a molar amount substantially equal to the succinic ester and is selected from metal hydrides and metal and alkoxides, and (iii) the reaction medium comprises an aprotic liquid medium or a protic liquid medium having a Ka, measured in water, lower than that of iPrOH.

Abstract: A process for the preparation of alkylidene substituted succinates comprising a step (a) in which is carried out the reaction of a carbonilic compound, a succinic and a base in a reaction medium and a step (b) in which the alkylidene substituted product obtained in (a) is esterified, characterized in that the succinic ester is used in a molar amount substantially equal to, or lower than, the amount of compound carbonilic compound, (ii) the base is used in a molar amount substantially equal to the succinic ester and is selected from metal hydrides and metal and alkoxides, and (iii) the reaction medium comprises an aprotic liquid medium or a protic liquid medium having a Ka, measured in water, lower than that of iPrOH.

Abstract: A new process is disclosed, particularly simple, convenient and practical, for the direct synthesis of metallocenes of formula (I): (CP)(ZR1m)n(A)rMLpL′q wherein (ZR1m)n is a divalent group bridging Cp and A; Cp is a substituted or unsubstituted cyclopentadieryl group; A is —O—, —S—, —N(R2)—, wherein R2 is hydrogen, alkyl, cycloalkyl aryl, alkylaryl or arylalkyl, or A has the same meaning of Cp; M is a transition metal belonging to group 3, 4, 5, 6 or to the lanthanide or actinide groups; L is a monoanionic sigma ligand, such as alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl, optionally containing Si or Ge; L′ is halogen or —OR5, R5 being a hydrocarbon radical; m is 1 or 2; n is 0-4; r is 0 or 1; p is 1-3; q is 0-2.