Abstract Impact polypropylene copolymers (IPC) are materials important for many commercial applications. These materials are usually synthetized by different methods involving two consecutive reactions: in liquid, gas or liquid-gas phase.… Click to show full abstract
Abstract Impact polypropylene copolymers (IPC) are materials important for many commercial applications. These materials are usually synthetized by different methods involving two consecutive reactions: in liquid, gas or liquid-gas phase. This work presents a method of synthesis in a laboratory scale based on two sequential steps in only one reactor in gas phase. Variables such as H2 addition, reaction time, and composition during the second step were studied, and their influence on the formation of propylene-ethylene copolymer materials with different properties was analyzed. The IPC materials so obtained were characterized by analytical temperature rising elution fractionation (TREF), calorimetric methods (DSC), 13C nuclear magnetic resonance (13C NMR), gel permeation chromatography with an infrared detector (GPC-IR5), Charpy impact, and scanning electron microscopy (SEM). The isotactic polypropylene matrix (iPP) obtained in the first step of the gas-phase process displays spherical morphology and lower mean particle size than those obtained in the liquid-phase process, even though the polymer grains experimented a certain tendency to agglomerate. In particular, hydrogen addition caused a significant decline in the catalyst productivity and dramatically shortened the length of the propylene homopolymer chains. Similarly, the presence of hydrogen on the synthesis of ethylene-propylene copolymers was demonstrated to lead to materials with very low molecular weight, low ethylene incorporation, and rubbery phases irregularly distributed along the iPP matrix and therefore with poor impact properties. On the other hand, ethylene-propylene copolymers synthesized without hydrogen yielded a suitable combination of molecular weights and molecular weight distribution that can contribute to good polymer processing and were proven to incorporate adequate amounts of ethylene mainly randomly distributed into the iPP matrix. SEM measurements revealed that the amorphous rubbery phase was homogeneously dispersed in the iPP matrix, and the Charpy test allowed to rank these materials as IPC. Finally, fractionation of IPC materials by preparative TREF provided information about the microstructure formation. Subsequent studying of molecular weights and composition of the fractions by GPC-IR, analytical TREF, and DSC measurements based on the ethylene-propylene composition and ethylene distribution in the molar mass molecules was shown to enable the design of IPC materials. Additionally, the optimal IPC material was compared with the best IPC using liquid-phase polymerization, and the results showed that the range of ethylene-propylene composition, as well as the ethylene distribution in IPC molar mass molecules, correlated with IPC mechanical behavior.
               
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