Fibre moulding

GFRP (chopped fibre, moulding grade) =37 =30 OK Creep above 60°C... 

Cellulose-based plastics, particularly cellulose nitrate and acetates, were the most commercially important semi-synthetics up to the 1940s and were used as the base for photographic film, textile fibres, moulded goods and in lacquers. Naturally occurring polymer cellulose in the form of cotton linters or wood pulp is chemically treated to increase its solubility. Cellulose has a high molecular weight of between 100000 and 500000 and an empirical formula C0H1OO5. Casein-formaldehyde is the only protein-based moulded plastic that achieved commercial success. It is based on cow s milk and is still produced in very small quantities for specialist items such as hand-coloured buttons. 

E Polyurethane Roving for thermoplastics - short-fibre moulding compounds (e.g. nylon)... 

Fig. 4.47. Zerodur lightweight mirror sample of 6lB4 mm in diameter and 72 mm in height, manufactured by direct casting by the use of a ceramic fibre mould. The weight reduction is 57% (faceplate thickness 12 mm, rib thickness 10 mm, cavity depth 60 mm, cavity width 50 mm)...

Typical Use Leather with ABS fibre-moulding materials. Typical Use Foams - polyurethane, PVC, phenolic-resin. Polyester, ... 

Comments FR = flame retardant, GF = glass fibres. Mould shrinkage for 6.4mm thickness, less for thinner samples. 

Polymeric vinylidene chloride generally produced by free radical polymerization of CH2 = CCl2. Homopolymers and copolymers are used. A thermoplastic used in moulding, coatings and fibres. The polymers have high thermal stability and low permeability to gases, and are self extinguishing. 

Polymers owe much of their attractiveness to their ease of processing. In many important teclmiques, such as injection moulding, fibre spinning and film fonnation, polymers are processed in the melt, so that their flow behaviour is of paramount importance. Because of the viscoelastic properties of polymers, their flow behaviour is much more complex than that of Newtonian liquids for which the viscosity is the only essential parameter. In polymer melts, the recoverable shear compliance, which relates to the elastic forces, is used in addition to the viscosity in the description of flow [48]. 

This includes wire enamels on a base of polyvinyl formal, polyurethane or epoxy resins as well as moulding powder plastics on phenol-formaldehyde and similar binders, with cellulose fillers, laminated plastics on paper and cotton cloth base, triacetate cellulose films, films and fibres of polyethylene terephthalate. 

This is also known as Bulk Moulding Compound (BMC). It is blended through a mix of unsaturated polyester resin, crosslinking monomer, catalyst, mineral fillers and short-length fibrous reinforcement materials such as chopped glass fibre, usually in lengths of 6-25 mm. They are all mixed in different proportions to obtain the required electromechanical properties. The mix is processed and cured for a specific time, under a prescribed pressure and temperature, to obtain the DMC. 

The generic thermosets are the epoxies and the polyesters (both widely used as matrix materials for fibre-reinforced polymers) and the formaldehyde-based plastics (widely used for moulding and hard surfacing). Other formaldehyde plastics, which now replace bakelite, are ureaformaldehyde (used for electrical fittings) and melamine-formaldehyde (used for tableware). 

Polymer-matrix composites for aerospace and transport are made by laying up glass, carbon or Kevlar fibres (Table 25.1) in an uncured mixture of resin and hardener. The resin cures, taking up the shape of the mould and bonding to the fibres. Many composites are based on epoxies, though there is now a trend to using the cheaper polyesters. 

For many applications (e.g. body pressings), it is inconvenient to use continuous fibres. It is a remarkable feature of these materials that chopped fibre composites (convenient for moulding operations) are nearly as strong as those with continuous fibres, provided the fibre length exceeds a critical value. 

New materials also emerged. Nylon, developed brilliantly by W. H. Carothers and his team of research workers for Du Pont as a fibre in the mid-1930s, was first used as a moulding material in 1941. Also in 1941 a patent taken out by Kinetic Chemical Inc. described how R. J. Plunkett had first discovered polytetrafluoroethylene. This happened when, on one occasion, it was found that on opening the valve of a supposedly full cylinder of the gas tetrafluoroethylene no gas issued out. On subsequently cutting up the cylinder it was found that a white solid, polytetrafluoroethylene (PTFE), had been deposited on the inner walls of the cylinder. The process was developed by Du Pont and, in 1943, a pilot plant to produce their product Teflon came on stream. 

Polymerisation casting involves mixing monomer or low molecular weight polymer with a polymerisation initiator, pouring the mix into the mould and allowing polymerisation to occur in situ. A variation is to impregnate fibres with initiated monomer or other low molecular weight material and polymerise to produce composite structures. The main problem is due to the heat of polymerisation. Unless heat transfer distances are kept short or unless the reaction is carried out very slowly it can easily get out of hand. 

Copolymers of chlorotrifluoroethylene and ethylene were introduced by Allied Chemicals under the trade name Halar in the early 1970s. This is essentially a 1 1 alternating copolymer compounded with stabilising additives. The polymer has mechanical properties more like those of nylon than of typical fluoroplastic, with low creep and very good impact strength. Furthermore the polymers have very good chemical resistance and electrical insulation properties and are resistant to burning. They may be injection moulded or formed into fibres. 

The early development of the nylons is largely due to the work of W. H. Carothers and his colleagues, who first synthesised nylon 66 in 1935 after extensive and classical researches into condensation polymerisation. Commercial production of this polymer for subsequent conversion into fibres was commenced by the Du Pont Company in December 1939. The first nylon mouldings were produced in 1941 but the polymer did not become well known in this form until about 1950. 

A low moulding shrinkage (0.005-0.007 cm/cm) in unfilled grades down to about 0.002 cm/cm in 30% glass-fibre-filled grades. 

The first commercial grades were introduced by Phillips Petroleum in 1968 under the trade name Ryton. These were of two types, a thermoplastic branched polymer of very high viscosity which was processed by PTFE-type processes and an initially linear polymer which could be processed by compression moulding, including laminating with glass fibre, and which was subsequently oxidatively cross-linked. 

In the late 1970s several developments occurred causing renewed interest in poly(ethylene terephthalate) as a plastics material. These included the development of a new mouldable grade by ICI (Melinar) and the development of a blow moulding technique to produce biaxially oriented PET bottles. In addition there appeared a glass-fibre filled, ionomer nucleated, dibenzoate plasticised material by Du Pont (Rynite) (see Chapter 26). 

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