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Polyethylene vinyl acetate

An important newer use of fluorine is in the preparation of a polymer surface for adhesives (qv) or coatings (qv). In this apphcation the surfaces of a variety of polymers, eg, EPDM mbber, polyethylene—vinyl acetate foams, and mbber tine scrap, that are difficult or impossible to prepare by other methods are easily and quickly treated. Fluorine surface preparation, unlike wet-chemical surface treatment, does not generate large amounts of hazardous wastes and has been demonstrated to be much more effective than plasma or corona surface treatments. Figure 5 details the commercially available equipment for surface treating plastic components. Equipment to continuously treat fabrics, films, sheet foams, and other web materials is also available. [Pg.131]

Chlorinated Polyethylene Polyethylene-Ethylacrylote Polyethylene-Vinyl acetate Polyethylene-Methacryllc Acid Polyphenyleneoxlde Poly-4 mef ylpentene(1) Polyethylene... [Pg.342]

Polyethylene vinyl acetate) Poly(methyl methacrylate) Polyethylene Polyurethanes... [Pg.27]

Polyvinyl chloride (PVC) Polyethylene vinyl acetate (EVA) Polyethylene terephthalate (PET)... [Pg.495]

Systems in which a polyolefin is the binder have attracted world-wide attention. These include the polyethylene—phenolic microsphere 74,115>, polyethylene or polypropylene—glass microsphere114116), polyethylene or polybutylene—PVC microsphere (containing isobutane)52), and polyethylene/vinyl acetate copolymer—glass microsphere11 systems. Syntactic foams have been made from polystyrene (and its copolymers with chlorostyrene or polychlorostyrene) and microspheres made from polyethylene or polypropylene46115 and foams from styrene/acrylonitrile 1171... [Pg.88]

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... [Pg.958]

Platform chemicals are compounds that serve as building blocks for numerous chemical intermediates and end products. An example is ethylene, which serves as the feedstock for derivatives such as acetaldehyde, ethylene dichloride, ethylene oxide, polyethylene, vinyl acetate, and ethyl acetate. Biobased chemicals such as succinic acid, 3-hydroxypropionic acid (3-HP), and butanol also have the potential to be converted into multiple derivatives, some of which are commodity chemicals and others that are higher-value chemicals. [Pg.878]

Talc particles of different lamellarity and specific surface area have been incorporated into polyethylene vinyl acetate (EVA) copolymer/magnesium hydroxide (MH) composite system.63 The fire retardancy of this system has been studied and compared with formulations containing only EVA and MH and formulations containing EVA, MH, and organomodified montmorillonites (oMMT). It was observed that talc with higher lamellar index showed fire behavior similar to that of EVA/MH/ oMMT system with some intumescence. [Pg.203]

Liquid colors are compatible with a wide variety of polymers, including PVC, polyethylene vinyl acetate (EVA), nylons, PET, polycarbonate, alloys, high-temperature polymers, and the full range of polyolefins and styrenics. Many liquid colors are suitable to color food-contact polymers and comply with all government regulations worldwide for shipping, use, and disposal. Lead times for liquid color are typically less than those for pellet or other melted color concentrates, since the processing is quick and efficient. [Pg.297]

D. Mnnteanu and S. Turcn, Evaluation of kinetic parameters of the thermal decomposition of polyethylene-vinyl acetate graft copolymers, J. Thermal Anal, 20, 281 (1981). [Pg.108]

FIGURE 9.6 Dependence of diffusion coefficients of various hydrocarbons in polybutadiene (PB) and polyethylene/vinyl acetate copol3fmer (EVAc) on molar volume of liquid hydrocarbons V. (From analysis of data presented in Kamiya, Y., Terada, K., Naito, Y., and Wang, J.S., J. Polym. Sci., B33, 1663, 1995.)... [Pg.238]

Examples of the use of nanostructured materials for packaging applications have been given in Chaudhry et al. (2008) and references therein. One of the first market entries into the food packaging arena was polymer composites containing clay nanoparticles (montmorillonite). The natural nanolayer structure of the clay particles impart improved barrier properties to the clay-polymer composite material. Some of the polymers which have been used in these composites for production of packaging bottles and films include polyamides, polyethylene vinyl acetate, epoxy resins, nylons, and polyethylene terephthalate. [Pg.201]

Polyethylene/ vinyl acetate/ graft acrylic acid Polybond 106 BP PO, PA, NBR... [Pg.66]

The three layers consisted of a fluoropol5mier inner layer, a polyolefin outer layer, and an intermediate tie layer that bonded them. The tie layer consisted of a polymer containing a blend of polyethylene-vinyl acetate and a block copolymer of styrene-ethylene-butadiene-styrene (SEES) or styrene-buta-diene-styrene (SBS) at a weight ratio in the range of 10 90 to 90 10. [Pg.245]

One of these types is the membrane-controlled transdermal therapeutic system, which is outlined in Figure 18.12. These systems consist of the following parts i) covering membrane, ii) drug reservoir, iii) micropore membrane controlling drug delivery, and iv) adhesive contact surface. (Further types of transdermal systems are going to be described in Chapter 16.2.4.3.3). The most commonly used membranes are polyethylene vinyl acetate and polyethylene [60-62]. [Pg.536]

Figure 9-33. Selectivity of different polymer membranes to He-N2 separation as a function of nitrogen permeability (n, incm /(cm x atm x s)) (1) polyvinylidenechloride (2,4)polyethylene terephthalafe (3) polyvinylfluoride (5) polyvinylchloride (6) polyamide (7) plasfified polyvinylidene chloride (8) cellulose nitrate (9) polypropylene (lO)fluoroplast (26) (ll)co-polymer of isoprene (74%) and acryl-nitryl (26%) (12, 18, 20) different co-polymers of butadiene and acryl-rritryl (13) polyacrylate (14) polycarbonate (15) polyisobutylene (16) bulyl latex (17) co-polymer of vinyl chloride and vinyl acetate (19, 37) butyl acetate of cellulose (21) polyethylene vinyl acetate (22) polybutadiene (23) special polymer SKI-3 (24) natural latex (25) nitryl silicon latex (26) dimethyl silicon latex (27) special polymer SKS-30 (28) special polymer SKMS-50 (29) special polymer SKMS-30 (30, 34, 35) high-density, medium-densily, and low-density polyethylene (31) polyethylene with 5% soot (32) co-polymer of ethylene (90%) and propylene (10%) (33) co-polymer of ethylene (96.5%) and vinyl acetate (3.5%) (36) triacetate of cellulose (38) acetate cellulose (39) polystyrene. Figure 9-33. Selectivity of different polymer membranes to He-N2 separation as a function of nitrogen permeability (n, incm /(cm x atm x s)) (1) polyvinylidenechloride (2,4)polyethylene terephthalafe (3) polyvinylfluoride (5) polyvinylchloride (6) polyamide (7) plasfified polyvinylidene chloride (8) cellulose nitrate (9) polypropylene (lO)fluoroplast (26) (ll)co-polymer of isoprene (74%) and acryl-nitryl (26%) (12, 18, 20) different co-polymers of butadiene and acryl-rritryl (13) polyacrylate (14) polycarbonate (15) polyisobutylene (16) bulyl latex (17) co-polymer of vinyl chloride and vinyl acetate (19, 37) butyl acetate of cellulose (21) polyethylene vinyl acetate (22) polybutadiene (23) special polymer SKI-3 (24) natural latex (25) nitryl silicon latex (26) dimethyl silicon latex (27) special polymer SKS-30 (28) special polymer SKMS-50 (29) special polymer SKMS-30 (30, 34, 35) high-density, medium-densily, and low-density polyethylene (31) polyethylene with 5% soot (32) co-polymer of ethylene (90%) and propylene (10%) (33) co-polymer of ethylene (96.5%) and vinyl acetate (3.5%) (36) triacetate of cellulose (38) acetate cellulose (39) polystyrene.
Figure 1. FTIR microscope spectra of kaolin vs. polyethylene vinyl acetate. Figure 1. FTIR microscope spectra of kaolin vs. polyethylene vinyl acetate.
ATR was the most consistent tool to obtain a good correlation of peak ratios to percent filler. We obtained a standard curve with an R squared value of0.995 using the kaolin peak at 540 cm and the CH2 stretch of polyethylene vinyl acetate at 2847 cm. The standard curve is shown in Figure 2 and the overlay of the ATR spectra for 1 to 50% filler is shown in Figure 3. Slunmary of results of the ashing of the samples is shown in Table 1. [Pg.194]

EVA, polyethylene + vinyl acetate TCB, 1,2,4-trichlorobenzene ODCB, 1,2-dichlorobenzene. [Pg.189]

Teflon 75% ciystalline Polyethylene-vinyl acetate copolymer Chlorosulfonated polyethylene Nylon 66... [Pg.897]

Vasudev, S. C., Chandy, T., and Sharma, C. P. 1997. Development of chitosan-polyethylene vinyl acetate comatrix Controlled release of aspirin-heparin for preventing cardiovascular thrombosis. Biomaterials 18 375-381. [Pg.460]

In a reported in vitro study of blood and cellular response to saturated AA-PEAs, the proliferation of endothelial cells adhered to SPEA substrates was much higher than on nonbiodegradable polymers like poly(n-butyl methacrylate) or polyethylene vinyl acetate copolymer (DeHfe et a/., 2005). [Pg.312]

Polyethylene vinyl acetate coated dyed Aesculap, Inc., USA of B. Braun... [Pg.331]

Analysis of Polyethylene Acrylate and Polyethylene-Vinyl Acetate Copolymers... [Pg.116]

Barrall and co-vv orkers [97] have described a PGC procedure for the analysis of PE-ethyl acrylate and PE-vinyl acetate copolymers and physical mixtures thereof. The pyrolysis chromatogram of polyethylene-vinyl acetate contains tw o principal peaks. The first is methane and the second acetic acid ... [Pg.116]

The pyrolysis chromatogram of polyethylene-ethyl acrylate at 475 C shows one principal peak due to ethanol. No variation in peak areas is noted in the temperature range 300-480 °C. Table 3.13 shows the analysis of 0.05 g samples of polyethylene-ethyl acrylate and polyethylene-vinyl acetate obtained at a pyrolysis temperature of 475 °C. [Pg.116]

Table 3.13 Pyrolysis results on physical mixtures of polyethylene-ethyl and polyethylene-vinyl acetate acrylate... Table 3.13 Pyrolysis results on physical mixtures of polyethylene-ethyl and polyethylene-vinyl acetate acrylate...

See other pages where Polyethylene vinyl acetate is mentioned: [Pg.124]    [Pg.122]    [Pg.224]    [Pg.61]    [Pg.495]    [Pg.29]    [Pg.86]    [Pg.10]    [Pg.86]    [Pg.290]    [Pg.220]    [Pg.193]    [Pg.64]    [Pg.344]    [Pg.1118]    [Pg.454]    [Pg.325]    [Pg.591]    [Pg.210]   
See also in sourсe #XX -- [ Pg.300 ]

See also in sourсe #XX -- [ Pg.33 ]




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