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Polyacrylate coating

As revealed by IR-spectroscopy, the attachment of the polymer proceeds via acylation of aminopropyls absorbances of both amides (1650 cm-1) and esters (1740 cm-1) contribute to the spectrum of polyacrylate-coated aminopropyl-Aerosil (specific surface area 175 m2/g) [55], During the reaction, the accumulation of p-nitrophenyl ester groups in the support is accompanied by the liberation of p-nitrophenol into the contacting solution. Thus, the evaluation of the conformational state of adsorbing macromolecules can be performed by the simultaneous study of both processes by UV-spectroscopy as shown in Fig. 7. Apparently, at... [Pg.155]

Vaes, H.J., C. Hamwijk, E.U. Ramos, H.J.M. Verhaar, and J.L.M. Hermens. 1996. Partitioning of organic chemicals to polyacrylate-coated solid phase. Anal. Chem. 68 44584 462. [Pg.63]

The data obtained clearly demonstrate that the scratch resistance of polyacrylate coating materials can be strongly enhanced by incorporation of methacryloyloxymethylsilanes (the reasons for the low value of gloss retention observed for 3c are not yet fully understood). As an additional benefit, the cured clearcoats revealed an extremely high chemical resistance no change in the films were observed after a 500 h exposure to 30% aq. H2SO4 test or after 100 cycles in the MEK rub test [4]. [Pg.739]

Fig. 4.28. Total ion current GC-MS chromatogram for BTX and phenol mixtures in water. (A) Extracted with a polydimethylsiloxane coating. (B) Extracted with a polyacrylate coating. K is the coating/water partition coefficient of the analyte, which drops by more than 2 orders of magnitude for o-xylene and increases by more than 1 for 2,4-dichlorophenol upon changing the coating from non-polar polydimethylsiloxane to polyacrylate. (Reproduced with permission of the American Chemical Society.)... Fig. 4.28. Total ion current GC-MS chromatogram for BTX and phenol mixtures in water. (A) Extracted with a polydimethylsiloxane coating. (B) Extracted with a polyacrylate coating. K is the coating/water partition coefficient of the analyte, which drops by more than 2 orders of magnitude for o-xylene and increases by more than 1 for 2,4-dichlorophenol upon changing the coating from non-polar polydimethylsiloxane to polyacrylate. (Reproduced with permission of the American Chemical Society.)...
SPE Carbopack cartridges (Envi-Carb (Carbopack B), 250 mg, Supelco, Bellafonte, CA, USA). SPME polyacrylate coated fiber (85 /am film thickness) from Supelco (Bellafonte, PA, USA)... [Pg.91]

Sorbent polyacrylate-coated fiber optimized by using a response surface generated with a Doehlert design... [Pg.95]

A -nitrosodibutylamina and A -nitrosodibenzylamina. This method is based on the isolation of the compounds by steam distillation, followed by the SPME in the distillate headspace using a polyacrylate coated silica fiber, and the determination by GC-TEA. Recoveries ranged between 41% and 112%. Nitrosamines in environmental matrixes (air, tobacco, and seawater) were preconcentrated on polydimethylsiloxane/divinylbenzene and the recovery of different nitrosamines from different matrixes varied between 95% and 98%. °" ... [Pg.428]

In one studyOPPs were extracted with SPME (85 /rm of polyacrylate coating) by the immersion technique at 75°C for 60 min. Desorption was done in a desorption device by supercritical fluid carbon dioxide (temperature 50°C pressure 306 atm) prior to online introduction into LC. The detection limits were 300 /rg/l for diazinon, 40 /rg/l for EPN, and 60 /rg/1 for chlorpyrifos, with recoveries ranging from 62 to 64%. [Pg.864]

Nitromethane is active chemically, can have many chemical reactions as a chemical reagent or synthesis intermediate. It also can be used as solvents for cellulose nitrate, cellulose acetate, cellulose acetate, vinyl resin, polyacrylate coating, beeswax, etc. base or other materials can be added into nitromethane for generate explosives when nitromethane is mixed with strong oxidant hydrogen peroxide or N2O4, it can be used as liquid rocket propellants and fuel nitromethane can also be used in medicine, dyes, insecticides, fungicides, stabilizers and surfactants. [Pg.149]

In principle, this method uses a fiber coated with an adsorbent that can extract organic compounds Irom the headspace above a liquid or solid sample. Extracted compounds are desorbed upon exposure of the SPME fiber in the heated injector port of a gas chromatograph (GC). SPME was carried out with a CTC Combi Pal system autoinjector at 70°C for 60 min using a fibre with an 85 pm polyacrylate coating. SPME sampling was done in the headspace above the surface of 5 ml diluted, acetate-buffered urine (containing 2 ml urine 2.5 ml water 0.5 ml 2 M acetate-buffer, pH 4.8 1.83 g NaCI, and 2 pg undecanoic acid as internal standard) in 20 ml headspace vials (Shimadzu). [Pg.112]

Bauer F, Flyunt R, CzUial K, Buchmeiser MR, Langguth H, Mehnert R (2006) NanoMicro particle hybrid composites for scratch and abrasion resistant polyacrylate coatings. Macromol Mater Eng 291(5) 493 98... [Pg.176]

Two types of SPME fibers (Supelco, Inc.) were evaluated for each analyte 100-pm polydimethyl-siloxane and 85-pm polyacrylate coatings. Samples were then analyzed directly by GC-MS (Varian Saturn IV D) or derivatized on fiber first, then analyzed by GC-MS. The on-fiber derivatization procedure is accomplished by gently coating the SPME fiber with N,0-bis(trimethylsilyl)-trifluoroacetamide (BSTFA) prior to GC-MS analysis. The sample matrices analyzed in this study included soil leachate (sandy loam, Oakley, CA), simulated sea water (Instant Ocean, Aquarium Systems Co., Mentor, OH), and canal water (rain runoff, Livermore, CA). The chemical signatures we selected for the proliferation of CW included dimethyl methylphosphonate (DMMP), diisopropyl methylphosphonate (DIMP), 1,4-dithiane, thiodiglycol (TDG), and 2-(diisopropylamino)ethanol (DIAE). [Pg.71]

LLE, liquid-liquid extraction MAE, microwave-assisted extraction SEE, solid-phase extraction SPME, solid-phase microextraction LPME, liquid-phase microextraction SOME, single-drop microextraction D-LLLME, dynamic liquid-liquid-liquid microextraction SEE, supercritical fluid extraction MIP, molecularly imprinted polymers sorbent SPMD, device for semipermeable membrane extraction PDMS, polydimethylsiloxane coated fiber PA, polyacrylate coated fiber CW-DMS, Carbowax-divinylbenzene fiber PDMS-DVB, polydimethylsiloxane divinylbenzene fiber CAR-PDMS, Carboxen-polydimethylsiloxane coated fiber DVB-CAR-PDMS, divinylbenzene Carboxen-polydimethylsiloxane coated fiber CW-TPR, Carbowax-template resin HS-SPME, headspace solid-phase microextraction MA-HS-SPME, microwave-assisted headspace-solid-phase microextraction HEM, porous hollow fiber membrane PEl-PPP, polydydroxylated polyparaphenylene. [Pg.470]

To extract very polar analytes from polar samples, use an 85 pm polyacrylate-coated fibre. [Pg.17]


See other pages where Polyacrylate coating is mentioned: [Pg.172]    [Pg.111]    [Pg.171]    [Pg.259]    [Pg.145]    [Pg.166]    [Pg.380]    [Pg.1634]    [Pg.314]    [Pg.579]   
See also in sourсe #XX -- [ Pg.579 ]




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Polyacrylate-coated fibers, solid-phase

Polyacrylate-coated fibers, solid-phase microextraction

Polyacrylates

Polyacrylic

Polyacrylics

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