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Shore polymers

The radiation and temperature dependent mechanical properties of viscoelastic materials (modulus and loss) are of great interest throughout the plastics, polymer, and rubber from initial design to routine production. There are a number of laboratory research instruments are available to determine these properties. All these hardness tests conducted on polymeric materials involve the penetration of the sample under consideration by loaded spheres or other geometric shapes [1]. Most of these tests are to some extent arbitrary because the penetration of an indenter into viscoelastic material increases with time. For example, standard durometer test (the "Shore A") is widely used to measure the static "hardness" or resistance to indentation. However, it does not measure basic material properties, and its results depend on the specimen geometry (it is difficult to make available the identity of the initial position of the devices on cylinder or spherical surfaces while measuring) and test conditions, and some arbitrary time must be selected to compare different materials. [Pg.239]

Urethanes are processed as mbber-like elastomers, cast systems, or thermoplastic elastomers. The elastomer form is mixed and processed on conventional mbber mills and internal mixers, and can be compression, transfer, or injection molded. The Hquid prepolymers are cast using automatic metered casting machines, and the thermoplastic peUets are processed like aU thermoplastic materials on traditional plastic equipment. The unique property of the urethanes is ultrahigh abrasion resistance in moderately high Shore A (75—95) durometers. In addition, tear, tensUe, and resistance to many oUs is very high. The main deficiencies of the urethanes are their resistance to heat over 100°C and that shear and sliding abrasion tend to make the polymers soft and gummy. [Pg.234]

Shear modulus, polyamide, 138 Sheet molding compounds (SMCs), 30 Shoe sole products, 205 Shore hardness gauge, 243 Side-chain liquid crystalline polymers, 49 Side reactions, in transition metal coupling, 477... [Pg.600]

Similar blends have been made by cross-linking the E-plastomer with peroxides. This process suffers from an inherent degradation of the iPP by peroxide. In a representative formulation, a mixture of 60 parts of E-plastomer (octene commoner), 15 parts maleated (0.6%) iPP, 25 parts of EPDM, 10 parts of paraffinic plasticizer, 5 parts of dicumyl peroxide, and 1 part of stabilizer was treated at 170°C for 5 min to give a cross-linked blend with Shore A hardness 66, tensile strength 5.5 MPa, and elongation 190%. Similar blends have been made with the incorporation of a limited amount of a SEES polymer to act as a compatibilizer between the E-plastomer and the iPP. [Pg.177]

The Photopolymer Plate of over 85° Shore D hardness can stand temperatures over 160°C, and it could be successfully used as a master plate for making thermoformed matrix of phenol group resin to be used for thermoformed polymer printing plates such as rubber plates and the like under conditions of 30 kg/cm2 pressure... [Pg.277]

The continuous availability of trillions of independent microreactors greatly multiplied the initial mixture of extraterrestrial organics and hydrothermal vent-produced chemicals into a rich variety of adsorbed and transformed materials, including lipids, amphiphiles, chiral metal complexes, amino add polymers, and nudeo-tide bases. Production and chiral amplification of polypeptides and other polymeric molecules would be induced by exposure of absorbed amino adds and organics to dehydration/rehydration cydes promoted by heat-flows beneath a sea-level hydro-thermal field or by sporadic subaerial exposure of near-shore vents and surfaces. In this environment the e.e. of chiral amino adds could have provided the ligands required for any metal centers capable of catalyzing enantiomeric dominance. The auto-amplification of a small e.e. of i-amino adds, whether extraterrestrially delivered or fluctuationally induced, thus becomes conceptually reasonable. [Pg.199]

Fluorel" Brand 2141 Elastometer of Minnesota Mining and Mfg Co, St Paul, Minn 55119 is a fully saturated fluorinated polymer contg more chan 60% F by wt auu is non-flammable. Lt colored gum, sp gr 1.85, shore A hard-... [Pg.502]

The so-called brittle point, associated with sample failure in impact tests, may be determined qualitatively using a penetrometer or a Shore durometer (an instrument used to measure resistance of a sample to penetration by a blunt needle) to measure the change in penetration hardness with temperature. Also, a thin film of a polymer may be readily folded at temperatures above T but may crack when folded at temperatures below Tr... [Pg.34]

For a discussion of the synthetic chemistry of B—H compounds, see Shore. S. C In Biafis. Clutters, tint] Polymers of the Main Croup Elements Cowley. A. H.. Ed. ACS Symposium Series 232, American Chemical Sociciy Washington. DC. 1983, j i Trimcthylbomr. unlike BHj. shows no tendency to dimerize... [Pg.930]

Substitute for Conventional Vulcanized Rubbers, For this application, the products are processed by techniques and equipment developed for conventional thermoplastics, ie, injection molding, extrusion, etc. The S—B—S and S—EB—S polymers are preferred (small amounts of S—EP—S are also used). To obtain a satisfactory balance of properties, they must be compounded with oils, fillers, or other polymers compounding reduces costs. Compounding ingredients and their effects on properties are given in Table 8. Oils with high aromatic content should be avoided because they plasticize the polystyrene domains. Polystyrene is often used as an ingredient in S—B—S-based compounds it makes the products harder and improves their processibility. In S—EB—S-based compounds, crystalline polyolefins such as polypropylene and polyethylene are preferred. Some work has been reported on blends of liquid polysiloxanes with S—EB—S block copolymers. The products are primarily intended for medical and pharmaceutical-type applications and hardnesses as low as 5 on the Shore A scale have been reported (53). [Pg.17]

Polymer Izod impact strength (j/m) 7f> (K) hard ness Ball indentation hardness (107 N/m2) Shore D hardness Friction coefficient (-) resistance (ASTM- D1044) (Taber) (mg/lOOOc) Abrasion loss factor (DIN 53516) (mg) Polymer ref. nr. in figures (cf. Table 13.12) ... [Pg.831]

Polymer System Shore Hardness Tensile Strength (MPa)... [Pg.654]

S. G. Shore, in Rings, Cages, Clusters and Polymers of the Main Group Elements, A. H. Cowley, ed., ACS Symposium Series No. 232, American Chemistry Society, Washington, DC 1983, p. 1. [Pg.257]

Table VI contains the general properties for 50-60% HARD SEGMENT polymers. This table contains polymers which have been developed in the past such as the Polyurethanes in the 55 to 65 Shore D hardness (Fascia materials), as well as Poly(urea-urethanes) which are more recent developments. This hard segment range also covers 65 to 75D intermediate modulus materials which are in reality toughened plastics. The raw materials prices are for comparison purposes. Table VI contains the general properties for 50-60% HARD SEGMENT polymers. This table contains polymers which have been developed in the past such as the Polyurethanes in the 55 to 65 Shore D hardness (Fascia materials), as well as Poly(urea-urethanes) which are more recent developments. This hard segment range also covers 65 to 75D intermediate modulus materials which are in reality toughened plastics. The raw materials prices are for comparison purposes.

See other pages where Shore polymers is mentioned: [Pg.443]    [Pg.302]    [Pg.358]    [Pg.17]    [Pg.20]    [Pg.528]    [Pg.53]    [Pg.243]    [Pg.266]    [Pg.163]    [Pg.163]    [Pg.330]    [Pg.453]    [Pg.95]    [Pg.104]    [Pg.302]    [Pg.20]    [Pg.175]    [Pg.285]    [Pg.68]    [Pg.44]    [Pg.67]    [Pg.222]    [Pg.487]    [Pg.4191]    [Pg.82]    [Pg.109]    [Pg.528]    [Pg.6]    [Pg.116]    [Pg.8]    [Pg.85]    [Pg.30]   
See also in sourсe #XX -- [ Pg.478 ]

See also in sourсe #XX -- [ Pg.478 ]




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