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Metallocene HDPE

KISS keep it short simple mHDPE metallocene HDPE (different... [Pg.652]

HDPE resias are produced ia industry with several classes of catalysts, ie, catalysts based on chromium oxides (Phillips), catalysts utilising organochromium compounds, catalysts based on titanium or vanadium compounds (Ziegler), and metallocene catalysts (33—35). A large number of additional catalysts have been developed by utilising transition metals such as scandium, cobalt, nickel, niobium, molybdenum, tungsten, palladium, rhodium, mthenium, lanthanides, and actinides (33—35) none of these, however, are commercially significant. [Pg.383]

Linear low-density polyethylene (LLDPE) is produced in the gas phase under low pressure. Catalysts used are either Ziegler type or new generation metallocenes. The Union Carbide process used to produce HDPE could be used to produce the two polymer grades. Terminal olefins (C4-C6) are the usual comonomers to effect branching. [Pg.328]

Obviously, there exists severe interplastics competition, e.g. PP vs. ABS, clarified PP vs. PS, PA, PVC, HDPE and PS (Table 10.7). A wide range of cross-linked and thermoplastic elastomer applications, from footware to automotive parts and toothbrushes, are adopting new metallocene-catalysed polyolefin elastomers (POEs). These low-density copolymers of ethylene and octene were first accepted as impact modifiers for TPOs, but now displace EPDM, (foamed) EVA, flexible PVC, and olefinic thermoplastic vulcanisates (TPVs). Interpolymer competition may also result from... [Pg.715]

As part of a multi-technique investigation (see also discussion under mid-infrared spectroscopy later), Corrales et al. [13] plotted the carbonyl index for films prepared from three grades of polyethylenes a high-density PE (HDPE), a linear low-density PE (LLDPE) and a metallocene PE (mPE) (see Figure 5). In this study, the data trend shown in Figure 5 correlated well with activation energies derived from the thermal analysis, which showed that the thermal-oxidative stability followed the order LLDPE > mPE > HDPE, whereas the trend... [Pg.394]

As discussed earlier under Section 2.3, Carbonyl index, in one relatively recent comparison of the photo-oxidative and thermal (oven-aged) degradation behaviour of different polyethylenes, additive free grades of a metallocene (mPE), an HDPE and a linear low-density PE (LLDPE) were analysed by a combination of mid-IR spectroscopy, TGA and CL [13]. The mid-IR... [Pg.403]

Metallocenes give polyethylene producers a long list of opportunities to work on. They have already created polyethylene copolymers that compete well in applications that have been formerly the exclusive domain of the more costly, so-called high value plastics. Further, they are augmenting the chromium oxide and Ziegler-Natta catalysts systems that have been used for HDPE and LLDPE with metallocene catalysts. That creates even further... [Pg.337]

A review is presented of the nitrogen autoclave process for the manufacture of crosslinked polyolefin foams. Process and product developments over the last few years are summarised and future possibilities are described. Process developments include use of higher temperatures and pressures to produce foams having densities as low as 10 kg/cub.m. Product developments include foams based on HDPE/LDPE blends, propylene copolymers and metallocene-catalysed ethylene copolymers. The structure and properties of these foams are compared with those of foams produced by alternative processes. 5 refs. [Pg.75]

Metallocene initiators reached commercialization near the beginning of the twenty-first century. These initiators probably accounted for about 5% of the total production of HDPE, LLDPE, and PP in 2002. The relative importance of metallocene initiators compared to the traditional Ziegler-Natta and Phillips-type initiators will increase in the future. [Pg.696]

Recycled HDPE items (blow-moulding grade) produced from HDPE made by the Phillips process were analysed by IR spectroscopy. The absorption bands at 888 and 965 cm-1, corresponding to unsaturations of vinylidene and vinylene type, respectively, are common in PE produced by either the Ziegler process or metallocenes [104]. The absence of these bands in the IR spectrum of the different samples confirmed that the resins had been produced using a Cr-type catalyst [118]. [Pg.220]

High-Density Polyethylene (HDPE). Polymerization of ethylene to polyethylenes is most often carried out at low temperature and pressure, using either the Ziegler aluminum triethyl plus titanium tetrachloride catalyst system, the Phillips chromic oxide plus silica plus alumina system, or more recently the newer metallocene single-site catalyst systems. [Pg.642]

Application The Innovene G (gas phase) process produces linear-low-density polyethylene (LLDPE) and high-density polyethylene (HDPE) using either Ziegler-Natta, chromium or metallocene catalysts. [Pg.152]

The tunable metallocene catalyst with a well-defined polymerization mechanism provides distinctive advantages in the preparation of new polymers with well-controlled molecular structures, especially functional polyolefins that are very difficult to prepare by other methods. Since the discovery of HDPE and i-PP about half a century ago, functionalization of polyolefin has been a scientifically challenging and industrially important area. The constant interest, despite lack of effective functionalization chemistry, is due to the strong desire to improve polyolefin s poor interactive properties. The hydrophobicity and low surface energy of polyolefin has limited its applications, especially in the areas of coating, blends, and composites, in which adhesion, comparability, dispersion, and paintability are paramount. [Pg.1606]

Ziegler-Natta catalysts are widely used in the production of high-density and linear low-density polyethylene (HDPE and LLDPE). More than half the world production of HDPE and over 90%o of LLDPE is based on Ziegler-Natta catalysts, although increased use of metallocene and other single-site catalysts is expected throughout the next decade. [Pg.3249]

The first reactor-type thermoplastic polyolefin (R-TPO) was LLDPE/PP [Yamazaki and Eujimaki, 1970, 1972]. The three-component R-TPO s (PE with PP and EPR) soon followed [Strametz et al, 1975]. PE was also polymerized in the presence of active catalyst and an olefinic copolymer [Morita and Kashiwa, 1981]. Blending amorphous co-polyolefins with crystalline PO s (HDPE, LLDPE, PP), and a filler resulted in moldable blends, characterized by excellent sets of properties [Davis and Valaitis, 1993, 1994]. Blends of polycycloolefin (PCO) with a block copolymer (both polymerized in metallocene catalyzed process) and PE, were reported to show outstanding properties, viz. strength, modulus, heat resistance and toughness [Epple and Brekner, 1994]. [Pg.51]

Polyethylene, LI7IVID/HDPE Polypropylene, Metallocene upgrade Polypropylene, Sheripol Polypropylene, Spherizone Polyethylene, HOPE... [Pg.29]

Impact-modifying additives designed to inaease the drop impaa resistance of rigid PP containers, for example, may also be chosen for how they affea darity. PO bottles require low-temperature drop-impact properties in particular, which can be enhanced with additions of metallocene plastomer modifiers. However, these modifiers can create haze if they have shown large enough differences in refractive index with the base resin. Specifically, in tests of HDPE bottles, plastomers with lower densities ( 0.900) were found to affea darity very little (20%-24% haze), whereas a 0.910-density plastomer produced "noticeable" haze (37%) [10-22]. [Pg.170]


See other pages where Metallocene HDPE is mentioned: [Pg.76]    [Pg.486]    [Pg.76]    [Pg.486]    [Pg.383]    [Pg.404]    [Pg.207]    [Pg.67]    [Pg.109]    [Pg.341]    [Pg.4]    [Pg.51]    [Pg.152]    [Pg.235]    [Pg.453]    [Pg.1145]    [Pg.14]    [Pg.16]    [Pg.226]    [Pg.1006]    [Pg.1041]    [Pg.108]    [Pg.1606]    [Pg.207]    [Pg.131]    [Pg.137]    [Pg.97]    [Pg.50]    [Pg.217]    [Pg.84]    [Pg.85]    [Pg.195]   
See also in sourсe #XX -- [ Pg.602 ]




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