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Sclair resins

Additive-free film samples of isotactic polypropylene (iPP, 30pm Himont Profax resin) and polyethylenes (LLDPE, 120ym, linear low density DuPont Sclair resin, and UHMW-PE, 120wm, ultra high molecular weight, high density Himont LSR 5641-1B resin) were oxidized by exposure in air to y-radiation (AECL Gamma Cell 220, 1.0... [Pg.377]

It appears that in these Sclair resins the increased crystallinity is the result of fewer, larger crystallites rather than more of the same size. These larger crystallites have a lower total surface area. The tortuosity is then relatively unaffected, but the chain immobilization factor defined by Equation 2 is reduced significantly, resulting in a larger diffusion coefficient in the denser, more crystalline materials. [Pg.255]

The Sclair resins under study here were of similar melt index and were manufactured under similar conditions. They are a uniform series of polyethylenes differing only in density. Microscopic observation under polarized light confirmed the hypothesis that the higher crystallinity in... [Pg.255]

Sclair resins results from fewer, larger crystallites. These results are given in Table II along with estimates of the specific surface area to which p is assumed proportional. Thus even in relatively well defined systems, diflFusion measurements provide new information on polymer structure. [Pg.256]

The first ELDPE (Sclaire resins) was produced by DuPont Canada Ltd. in a solution process using Z-N vanadium (V) catalyst 0 0-n butyl)2 Cl, and A1 (Et)i li.5. The comonomer was C4-20. with the Al/V ratio increasing with comonomer MW from 5 1 to 12 1... [Pg.1642]

Polyethylene. The effect of crystallinity on the diffusion coefficient of iso-octane at 54°C in PE was determined in a sorption experiment. Films of Sclair PE (DuPont Chemical Co., Kingston, Ontario) were compression-molded in a hot platens press at 170°C and were allowed to cool in the press. All films were 200 /xm thick. The properties of the resins are given in Table II. [Pg.248]

Novapol LF-0717-A Sclair 69A resin, gloss overlacquers Pliolite VTAC... [Pg.1589]

A Petrothene NA 220-000 Sclair 69A resin, thermopiastic chem.-resistance... [Pg.1589]

Schulink, Crosslinkable polyethylene rotational molding compound, Schulman, A., Inc. SCLAIR, Polyethylene resins, NOVA Chemicals Ltd. [Pg.933]

Sanoprene. TP elastomer. Monsanto Co. Saran. PVDC resin. Dow Chemical Co. ScLAiR. Linear PE resin. Du Pont. [Pg.927]

DuPont s Sclair process was extremely important technology which was introduced in the 1960s, as it offered commercial ethylene copolymers at densities as low as 0.916 g/cc with improved physical properties over comparable polyethylene resins produced with the high-pressure process. In addition, DuPont scientists also developed improved catalysts for the Sclair process based on vanadium compounds that produced homogeneous branching distribution of the short-chain branches introduced along the polymer backbone by incorporation of a comonomer such as 1-butene into the polymer structure. [Pg.296]

The first commercial process for making LLDPE was the Sclair technology developed by Dupont Canada and now implemented by NOVA Chemicals. This process involves high-temperature solution polymerization. Much LLDPE is now made in gas-phase reactors with butene or hexene as the co-monomer. The constrained-geometry catalyst (CGC) is a metallocene catalyst developed by Dow Chemical for the manufacture of linear, very-low density polyethylene resins by solution polymerization with octene as the comonomer. For a given co-monomer content, the solid-state density is lower for octene than for lower a-olefins. [Pg.71]


See other pages where Sclair resins is mentioned: [Pg.403]    [Pg.249]    [Pg.111]    [Pg.1470]    [Pg.1588]    [Pg.1589]    [Pg.1589]    [Pg.2335]    [Pg.25]   
See also in sourсe #XX -- [ Pg.255 ]




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