Fiber reinforced polymers reinforcement

Development of FRP (Fiber-reinforced polymer) -reinforced polymer concrete structural members [81-82]... 

Blontrock, H., F. Taerwe and S. Matthys (1999). Properties of fibre reinforced plastics at elevated temperatures with regard to fire resistance of reinforced concrete members. Fourth International Symposium on Fiber Reinforced Polymer Reinforcement for Concrete Structures, Farmington HUls, MI, pp. 43-54. 

International Symposinm on Fiber Reinforced Polymer Reinforcement for Concrete Stmctnres (FRPRCS)... 

Schock American Concrete Institute (ACI) - Committee 440 (Fiber-Reinforced Polymer Reinforcement)... 

Hacha, R., and Rizkalla, S.H. (2004). Near-surface-mounted fiber reinforced polymer reinforcements for flexural strengthening of concrete structures . ACI Structural Journal, 101(5) 717-726. 

The industrial value of furfuryl alcohol is a consequence of its low viscosity, high reactivity, and the outstanding chemical, mechanical, and thermal properties of its polymers, corrosion resistance, nonburning, low smoke emission, and exceUent char formation. The reactivity profile of furfuryl alcohol and resins is such that final curing can take place at ambient temperature with strong acids or at elevated temperature with latent acids. Major markets for furfuryl alcohol resins include the production of cores and molds for casting metals, corrosion-resistant fiber-reinforced plastics (FRPs), binders for refractories and corrosion-resistant cements and mortars. 

Crystalline polymers undergo a discontinuous decrease in volume when cooled through (Fig. 4). This can lead to nonuniform shrinkage and warping in molded objects. On the other hand, it also causes the polymer to "lock on" to reinforcing fibers, eg, glass (qv), so that crystalline thermoplastics benefit much more than amorphous thermoplastics from fiber reinforcement. 

Hand Lay-Up and Spray-Up. In hand lay-up, fiber reinforcements in mat or woven form are placed on the mold surface and then saturated with a Hquid polymer, typicaHy a polyester resin, that has been chemically activated to polymerize (cure) without the addition of heat. Multiple pHes of reinforcement and multiple cure steps aHow very heavy waH thicknesses to be achieved. 

Most processors of fiber-reinforced composites choose a phenol formaldehyde (phenoHc) resin because these resins are inherently fire retardant, are highly heat resistant, and are very low in cost. When exposed to flames they give off very Htde smoke and that smoke is of low immediate toxicity. PhenoHc resins (qv) are often not chosen, however, because the resole types have limited shelf stabiHty, both resole and novolac types release volatiles during their condensation cure, formaldehyde [50-00-0] emissions are possible during both handling and cure, and the polymers formed are brittle compared with other thermosetting resins. 

Some of the common types of plastics that ate used ate thermoplastics, such as poly(phenylene sulfide) (PPS) (see Polymers containing sulfur), nylons, Hquid crystal polymer (LCP), the polyesters (qv) such as polyesters that ate 30% glass-fiber reinforced, and poly(ethylene terephthalate) (PET), and polyetherimide (PEI) and thermosets such as diaHyl phthalate and phenoHc resins (qv). Because of the wide variety of manufacturing processes and usage requirements, these materials ate available in several variations which have a range of physical properties. 

Slotted plate for catalyst support designed with openings for vapor flow Ion exchanger fibers (reinforced ion exchange polymer) used as solid-acid catalyst None specified Hydrolysis of methyl acetate Evans and Stark, Eiir. Pat. Appl. EP 571,163 (1993) Hirata et al., Jap. Patent 05,212,290 (1993)... 

The single-curve blade (Fig. 18-41d) was developed for incorporating fiber reinforcement into pasties. In this application, the individual fibers (e.g., sisal or glass) must be wetted with polymer without incurring undue fiber breakage. 

The actual experimental moduli of the polymer materials are usually about only % of their theoretical values [1], while the calculated theoretical moduli of many polymer materials are comparable to that of metal or fiber reinforced composites, for instance, the crystalline polyethylene (PE) and polyvinyl alcohol have their calculated Young s moduli in the range of 200-300 GPa, surpassing the normal steel modulus of 200 GPa. This has been attributed to the limitations of the folded-chain structures, the disordered alignment of molecular chains, and other defects existing in crystalline polymers under normal processing conditions. 

A better combination of fiber and polymer is achieved by an impregnation of [44] the reinforcing fabrics with polymer matrixes compatible with the polymer. Polymer solutions [40,45] or dispersions [46] of ]ow viscosity are used for this purpose. For a number of interesting polymers, the lack of solvents limits the use of the method of impregnation [44]. When cellulose fibers are impregnated with a bytyl benzyl phthalate plasticized polyvinylchloride (PVC) dispersion, excellent partitions can be achieved in polystyrene (PS). This significantly lowers the viscosity of the compound and the plasticator and results in cosolvent action for both PS and PVC [46]. 

Organosilanes are the main group of coupling agents for glass fiber-reinforced polymers. They have been developed to couple virtually any polymer to the minerals that are used in reinforced composites f42J. 

Table 13 Mechanical Properties of Flax Fiber Reinforced Biologically Degradable Polymers (BDG) [72]...

Dumas ( .Series 6000 ), H V ( Hovosorb 11 ), Technical Fiber Products ( Polymer Reinforced Sealable Separator ). Nippon Glass Fiber ( MFC ) and Whatman also offer products with organic fibers and/or binders. 

Performance of plastics , W. Brostow Hanser Gardner Pubis (1999) ISBN 1569902771. Comprehensively covers the behavior of the most important polymer materials. Subject areas range from Computer Simulations of Mechanical Behavior to Reliability and Durability of aircraft structures made of fiber-reinforced hydrocarbons. 

A broad variety of structural polymers is nowadays available that are suitable for applications as different as carbon fiber reinforced materials, encapsulation of electronic devices or adhesive bonding. Each of these polymers belongs to one of two classes thermosets or thermoplastics. 

Short fiber reinforcement of TPEs has recently opened up a new era in the field of polymer technology. Vajrasthira et al. [22] studied the fiber-matrix interactions in short aramid fiber-reinforced thermoplastic polyurethane (TPU) composites. Campbell and Goettler [23] reported the reinforcement of TPE matrix by Santoweb fibers, whereas Akhtar et al. [24] reported the reinforcement of a TPE matrix by short silk fiber. The reinforcement of thermoplastic co-polyester and TPU by short aramid fiber was reported by Watson and Prances [25]. Roy and coworkers [26-28] studied the rheological, hysteresis, mechanical, and dynamic mechanical behavior of short carbon fiber-filled styrene-isoprene-styrene (SIS) block copolymers and TPEs derived from NR and high-density polyethylene (HOPE) blends. 

Though short fiber-reinforced mbber composites find application in hose, belt, tires, and automotives [57,98,133,164] recent attention has been focused on the suitability of such composites in high-performance applications. One of the most important recent applications of short fiber-mbber composite is as thermal insulators where the material will protect the metallic casing by undergoing a process called ablation, which is described in a broad sense as the sacrificial removal of material to protect stmcrnres subjected to high rates of heat transfer [190]. Fiber-reinforced polymer composites are potential ablative materials because of their high specific heat, low thermal conductivity, and ability of the fiber to retain the char formed during ablation [191-194]. 

---