Styrene resin

Fig. 6. Bed expansion as affected by resin type, flow rate, and temperature, where A represents a strong base styrenic resin in the CF form at 4°C, and B...

ABS (acrylonitrile—butadiene-styrene) resins are two-phase blends. These are prepared by emulsion polymerization or suspension grafting polymerization. Products from the former process contain 20—22% butadiene those from the latter, 12—16%. 

H. E. Frey and S. Stai, CEH Marketing Research Report, Mcrylonitrile—Puta ene—Styrene Resins, Stanford Research Institute, Menlo Park, Calif., p. 

Adhesives, Coatings, and Sealants. Eor these appHcations, styrenic block copolymers must be compounded with resins and oils (Table 10) to obtain the desired properties (56—58). Materials compatible with the elastomer segments soften the final product and give tack, whereas materials compatible with the polystyrene segments impart hardness. The latter are usually styrenic resins with relatively high softening points. Materials with low softening points are to be avoided, as are aromatic oils, since they plasticize the polystyrene domains and reduce the upper service temperature of the final products. 

Worldwide sales of poly(phenylene ether)—styrene resin alloys are 100,000—160,000 t/yr (47,96) aimual growth rates are ca 9%. Other resin, particularly acrylonitrile—butadiene—styrene (ABS) polymers and blends of these resins with PC resins, compete for similar appHcations. 

Aliphatic Polyolefins other than Polyethylene, and Diene Rubbers II.7.4.1 High-styrene resins ... 

Butadiene and styrene may be polymerised in any proportion. The Tfs of the copolymers vary in an almost linear manner with the proportion of styrene present. Whereas SBR has a styrene content of about 23.5% and is rubbery, copolymers containing about 50% styrene are leatherlike whilst with 70% styrene the materials are more like rigid thermoplastics but with low softening points. Both of these copolymers are known in the rubber industry as high-styrene resins and are usually used blended with a hydrocarbon rubber such as NR or SBR. Such blends have found use in shoe soles, car wash brushes and other mouldings but in recent times have suffered increasing competition from conventional thermoplastics and to a less extent the thermoplastic rubbers. 

Hard products may also be made by vulcanising rubber (natural or synthetic) using only about two parts of sulphur per 100 parts of rubber. In these cases either the so-called high-styrene resins or phenolie rubber compounding resins are ineorporated into the formulation. These compounds are processed using the methods of rubber technology but, like those of ebonite, the produets are more akin to plastics than to rubbers. Examples of the usage of these materials are to be found in battery boxes, shoe heels and ear washer brushes. 

Class and Chu [34] have studied the tackification of natural rubber and SBR over a wide range of resin concentrations for several tackifiers. From their graphical data it can be estimated that 1 1 tackification (by weight) with a poly(/-butyl styrene) resin, MW 850 and Tg = 59°C, gives a PSA with Tg about — 13°C, and storage modulus, G about 8.8 x 10 Pa, well within the PSA window. 

Isocyanates can be added to solvent-borne CR adhesive solutions as a two-part adhesive system. This two-part adhesive system is less effective with rubber substrates containing high styrene resin and for butadiene-styrene block (thermoplastic rubber) copolymers. To improve the specific adhesion to those materials, addition of a poly-alpha-methylstyrene resin to solvent-borne CR adhesives is quite effective [76]. An alternative technique is to graft a methacrylate monomer into the polychloroprene [2]. 

One of the most important solution blend polymers is high-styrene resin, which is manufactured by several companies worldwide. This is a latex blend of high-styrene rubber and normal styrene butadiene rubber. The different high-styrene master batches are available in the world as ... 

Dow ABS Nylon 6/6 Polycarbonate Polyethylene, HDPE, LDPE, LLDPE, ULDPE Polypropylene HPPP, CPPP Polystyrene HIPS, GPPS, Recycled, Advanced Styrenic Resin SAN Polyurethane Elastomers Polyolefin Plastomer PC/ABS Crystalline Polymer ABS/TPU... 

Preparation and Cure of Unsaturated Polyester/Styrene Resin... 

Unsaturated polyesters (UPs), 4, 18, 19 from PET waste, 560-561 Unsaturated polyester/styrene resin, preparation and cure of, 101 Unsaturated polyester thermosetting resins, syntheses of, 101-103 Unstirred interfacial process, 155 U-Polymer, 77... 

Acrylic Sheet (e.g. Perspex) Acrylonitrile Butadiene Styrene Resins (1) Nylon 66 Fibre (m) Nylon 66 Plastics (m) PCTFE PTFE (n) PVDF (y) Rigid Unplasticised PVC Plasticised PVC ... 

Acrylonitrile butadiene styrene resins The information refers to a general purpose moulding grade material. 

A chemical compound consisting of groups of atoms which are repeated almost indefinitely until very high molecular weights are achieved. High Styrene Resins... 

Compounding ingredients which bring about reinforcement of rubbers. The most widely used are carbon black, silica and silicates, zinc oxide, treated whitings, high styrene resins and phenolic resins. 

Blends of natural rubber or styrene-butadiene rubber with high styrene resins used as soling material in footwear manufacture. Such resin rubbers should not be confused with... 

Microcellular Rubber A product usually used for shoe soling application produced by the incorporation of a blowing agent into the high styrene resin soling compound. 

ABS resins, 23 370, 371. See also Acrylonitrile-butadiene-styrene resins... 

Styrenic monomers, 23 348-349 amine-containing, 20 473-475 Styrenic resins, 14 380, 399, 24 714 Styrenics... 

We have found the combination of the azide compound and the styrene resin is well suited for achieving high resolution and high aspect ratio patterns using KrF excimer laser stepper system, because of the absence of swelling-induced pattern deformation during alkaline development and the suitable optical density at 248 nm in terms of sensitivity. 

The azide compound was mixed with the styrene resin in the range of 10 to 40 wt%, and dissolved in 2-methoxy-ethyl acetate. 

Figure 2 shows the exposure characteristics for azide-styrene resin resist film with an azide concentration from 10 to 40 wt% (based on the styrene resin weight) and Figure 3 shows the contrast of the resist films as a function of the azide concentration. Development was done with a 60s immersion in 0.83% TMAH solution. The styrene resin matrix alone has been found to be a negative deep UV resist. However, rather low contrast (1.48) and low sensitivity (2.5 J/cm2) are observed. The contrast and the sensitivity of the styrene resin is remarkedly increased by adding the azide, as shown in Figures 2 and 3. 

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