Polypropylene additives

Polyethylene microstructure is defined by its distributions of chain length (CLD) or molecular weight (MWD), chemical composition (CCD), comonomer sequence length (CSLD), and LCB. In addition, polypropylene microstructure is further characterized by its distribution of regio- and stereoregularity [53, 54]. 

R F Becker, L P J Burton and S E Amos, Additives , Polypropylene Handbook, ed. E P Moore, Munich, Hanser, 1996, Chapter 4. 

Table 6.4 Effect of addition polypropylene of Lewis bases on the amount of crystalline fraction in ...

Pulp-like olefin fibers are produced by a high pressure spurting process developed by Hercules Inc. and Solvay, Inc. Polypropylene or polyethylene is dissolved in volatile solvents at high temperature and pressure. After the solution is released, the solvent is volatilised, and the polymer expands into a highly fluffed, pulp-like product. Additives are included to modify the surface characteristics of the pulp. Uses include felted fabrics, substitution in whole or in part for wood pulp in papermaking, and replacement of asbestos in reinforcing appHcations (56). 

Olefin Polymers. The flame resistance of polyethylene can be increased by the addition of either a halogen synergist system or hydrated fillers. Similar flame-retarder packages are used for polypropylene (see Olefin polymers). Typical formulations of the halogen synergist type are shown in Table 15 the fiUer-type formulations are in Table 16. 

This compound, designated Cyagard RF1204, has been recommended for use in polypropylene. Despite its high hydroxyl content, it is proposed not as a polyol but as a stable, high melting additive for polypropylene (108). 

Lamination Inks. This class of ink is a specialized group. In addition to conforming to the constraints described for flexo and gravure inks, these inks must not interfere with the bond formed when two or more films, eg, polypropylene and polyethylene, are joined with the use of an adhesive in order to obtain a stmcture that provides resistance properties not found in a single film. Laminations are commonly used for food applications such as candy and food wrappers. Resins used to make this type of ink caimot, therefore, exhibit any tendency to retain solvent vapor after the print has dried. Residual solvent would contaminate the packaged product making the product unsalable. 

The electrowinning process developed by Ginatta (34) has been purchased by M.A. Industries (Atlanta, Georgia), and the process is available for licensing (qv). MA Industries have also developed a process to upgrade the polypropylene chips from the battery breaking operation to pellets for use by the plastics industry. Additionally, East Penn (Lyons Station, Pennsylvania), has developed a solvent-extraction process to purify the spent acid from lead—acid batteries and use the purified acid in battery production (35). 

The uses of spunbonded fabrics as coverstock in diapers and other personal absorbent devices will most likely remain unchallenged for the near term. Virtually any other nonwoven production method appears to be at a cost disadvantage opposite spunbonded polypropylene. There have been composite products developed from meltblown and spunbonded combinations, where areas of either improved hydrophobicity or hydrophilicity are desired. These products can be produced on-line at relatively low additional cost and offer high value to diaper manufacturers. Any competitive threat is likely to come from advances in film technology such as large improvements in perforated film used in segments of absorbent product appHcations, particularly sanitary napkins. 

Polypropylene polymers are typically modified with ethylene to obtain desirable properties for specific applications. Specifically, ethylene—propylene mbbers are introduced as a discrete phase in heterophasic copolymers to improve toughness and low temperature impact resistance (see Elastomers, ETHYLENE-PROPYLENE rubber). This is done by sequential polymerisation of homopolymer polypropylene and ethylene—propylene mbber in a multistage reactor process or by the extmsion compounding of ethylene—propylene mbber with a homopolymer. Addition of high density polyethylene, by polymerisation or compounding, is sometimes used to reduce stress whitening. In all cases, a superior balance of properties is obtained when the sise of the discrete mbber phase is approximately one micrometer. Examples of these polymers and their properties are shown in Table 2. Mineral fillers, such as talc or calcium carbonate, can be added to polypropylene to increase stiffness and high temperature properties, as shown in Table 3. 

Disposable polypropylene nonwoven fabrics are widely used as the coverstock for disposable baby diapers. The expansion of the disposable diaper market throughout the world has been the primary source of growth in the consumption of polypropylene in the fiber market. In addition, nonwoven polypropylene fabrics are used in a variety of other disposable sanitary products, such as baby wipes, adult incontinence, and feminine hygiene products. Use of polypropylene nonwovens in disposable medical apparel, such as surgical gowns, has increased as a means of reducing the spread of infection. 

Increasingly, plastics are being used as parenteral packaging (qv) materials. Plastics such as poly(vinyl chloride), polyethylene, and polypropylene are employed. However, plastics may contain various additives that could leach into the product, such as plasticizers (qv) and antioxidants. PermeabiUty of plastics to oxygen, carbon dioxide, and water vapor must be tested in the selection of plastic containers. Furthermore, the plastic should withstand sterilization. Flaking of plastic particles should not occur and clarity necessary for inspection should be present. 

Polyolefins. Interest has been shown in the plasticization of polyolefins (5) but plasticizer use generally results in a reduction of physical properties (12), and compatibiHty can be achieved only up to 2 wt %. Most polyolefins give adequate physical properties without plasticization. There has been use of plasticizers with polypropylene to improve its elongation at break (7) although the addition of plasticizer can lower T, room temperature strength, and flow temperature. This can be overcome by simultaneous plasticization (ca 15 wt % level) and cross-linking. Plasticizers used include DOA. 

The use of TAG as a curing agent continues to grow for polyolefins and olefin copolymer plastics and mbbers. Examples include polyethylene (109), chlorosulfonated polyethylene (110), polypropylene (111), ethylene—vinyl acetate (112), ethylene—propylene copolymer (113), acrylonitrile copolymers (114), and methylstyrene polymers (115). In ethylene—propylene copolymer mbber compositions. TAG has been used for injection molding of fenders (116). Unsaturated elastomers, such as EPDM, cross link with TAG by hydrogen abstraction and addition to double bonds in the presence of peroxyketal catalysts (117) (see Elastol rs, synthetic). 

Propjiene [115-07-17, CH2CH=CH2, is perhaps the oldest petrochemical feedstock and is one of the principal light olefins (1) (see Feedstocks). It is used widely as an alkylation (qv) or polymer—ga soline feedstock for octane improvement (see Gasoline and other motor fuels). In addition, large quantities of propylene are used ia plastics as polypropylene, and ia chemicals, eg, acrylonitrile (qv), propylene oxide (qv), 2-propanol, and cumene (qv) (see Olefin POLYMERS,polypropylene Propyl ALCOHOLS). Propylene is produced primarily as a by-product of petroleum (qv) refining and of ethylene (qv) production by steam pyrolysis. 

Polymerization Reactions. Polymerization addition reactions are commercially the most important class of reactions for the propylene molecule and are covered in detail elsewhere (see Olefin polymers, polypropylene). Many types of gas- or liquid-phase catalysts are used for this purpose. Most recently, metallocene catalysts have been commercially employed. These latter catalysts requite higher levels of propylene purity. 

By employing additives to improve interfacial adhesion and the cohesive strength of the mbber phase, natural mbber can compete with ethylene—propylene mbbers as an impact modifier for polypropylene. These hard grades, containing between 15 and 25% natural mbber, have the potential for use in the automotive and domestic markets, eg, in bumpers, spoilers, grilles, electrical connectors, and floor tiles. 

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