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Poly propanesulfonate

The GBR resin works well for nonionic and certain ionic polymers such as various native and derivatized starches, including sodium carboxymethylcel-lulose, methylcellulose, dextrans, carrageenans, hydroxypropyl methylcellu-lose, cellulose sulfate, and pullulans. GBR columns can be used in virtually any solvent or mixture of solvents from hexane to 1 M NaOH as long as they are miscible. Using sulfonated PDVB gels, mixtures of methanol and 0.1 M Na acetate will run many polar ionic-type polymers such as poly-2-acrylamido-2-methyl-l-propanesulfonic acid, polystyrene sulfonic acids, and poly aniline/ polystyrene sulfonic acid. Sulfonated columns can also be used with water glacial acetic acid mixtures, typically 90/10 (v/v). Polyacrylic acids run well on sulfonated gels in 0.2 M NaAc, pH 7.75. [Pg.400]

Figure 2 Stability of /3-poly(L-malate) measured by its activity to inhibit purified DNA polymerase a of P. polyceph-alum. The relative degree of inhibition is shown (100 rel. units refer to complete inhibition). The DNA polymerase assay was carried out in the presence of 5 /tg/ml /S-poly(L-malate) as described [4]. The polymer was preincubated for 7 days at 4°C in the following buffer solutions (50 mM) KCl/HCl (—A—). Citrate (—V—). 2-(A/-Morpholino)-ethanesulfonic acid, sodium salt (—O—). Sodium phosphate (— —). N-(2-Hydroxyethyl)piperazine-N -(2-ethanesul-fonic acid), sodium salt (— — ). N,N-b s (2-Hydroxyethyl)-glycine, sodium salt (—T—). Tris/HCl (— —). 3-(Cyclo-hexylamino)-l-propanesulfonic acid, sodium salt (— —). Figure 2 Stability of /3-poly(L-malate) measured by its activity to inhibit purified DNA polymerase a of P. polyceph-alum. The relative degree of inhibition is shown (100 rel. units refer to complete inhibition). The DNA polymerase assay was carried out in the presence of 5 /tg/ml /S-poly(L-malate) as described [4]. The polymer was preincubated for 7 days at 4°C in the following buffer solutions (50 mM) KCl/HCl (—A—). Citrate (—V—). 2-(A/-Morpholino)-ethanesulfonic acid, sodium salt (—O—). Sodium phosphate (— —). N-(2-Hydroxyethyl)piperazine-N -(2-ethanesul-fonic acid), sodium salt (— — ). N,N-b s (2-Hydroxyethyl)-glycine, sodium salt (—T—). Tris/HCl (— —). 3-(Cyclo-hexylamino)-l-propanesulfonic acid, sodium salt (— —).
The first demonstration of a PEM with electrochromic properties was disclosed by SchlenofFand coworkers [66], using poly(butanylviologen)/ PSS films. While this film exhibited strong electrochromic response, it still required the use of an outer electrolyte solution. DeLongchamp and Hammond disclosed for the first time a solid-state device comprised of two electrochromic PEM-modified ITO electrodes separated by a 200-p,m thick poly(2-acrylamido-methane-2-propanesulfonic acid), proton-conducting PAMPS membrane (see Eigure 2.30) [196]. Both PEMs used in... [Pg.105]

In this study, we report the release properties of two new polyelectrolyte materials poly(acrylamido-methyl-propanesulfonate) (PAMPS) and poly (diallydimethyl ammonium chloride) (PDADMAC), which were used as anionic and cationic carriers, respectively, for oppositely charged drugs. These polymers proved to be very promising and practical as erodible carriers for controlled drug delivery as they are available commerically. Binding ionic moieties to the linear polymer backbone can be done by a simple mixing process. [Pg.79]

An anesthetic drug, Richlocaine, developed jointly by scientists from Kazakhstan and Russia, and commercially available biologically active substances bovine serum albumin, lysozyme, and catalase were used. Hydrogels of acrylamide and acrylic acid copolymer(AA-AAc),poly(N-isopropylacrylamide)(PNIPA),N-isopropylacrylamide and acrylic acid copolymer (NlPA-AAc), N-isopropylacrylamide and 2-(acrylamido)-2-propanesulfonic acid copolymer (NIPA-APSA) were synthesized. Diffusion parameters of bioactive substances into hydrogel matrices were calculated using Eq. (19.1) ... [Pg.180]

Although polymeric solvents have previously been prepared, they are usually based on pyridine, imidazole, or styrene and have the physical forms of a glass or a sticky rubber. Agents in the current application are liquids. Once dissolved poly(2-acrylamido-2-methyl-l-propanesulfonic acid) oxyethylene ammonium salts, however, can be directly converted into fabrics. [Pg.33]

Preparation of poly(2-acrylainido-2-methyl-l-propanesulfonic acid) oxyethylene ammonium salt... [Pg.34]

Poly(2-acrylamido-2-methyl-l-propanesulfonic acid and isopropylhexafluor-oalcohol), (IV), was prepared by Khojasteh et al. (4) and used as a top antireflective coating and barrier layer for immersion lithography. [Pg.557]

Fig. 6.2. Electrochromatographic separation of benzyl alcohol (1), resorcinol (2), methylparaben (3), and p-naphthol (4) using a soft gel column (Reprinted with permission from [27], Copyright 1998 Wiley-VCH). Conditions Column 48.5 cm (24 cm active) x 75 pm i.d., stationary phase 4.1% T, 9.7% C, 0.7% S poly(2-acrylamido-2-methyl-l-propanesulfonic acid-co-N-isopropyl acrylamide-co-methylene bisacrylamide) mobile phase 20 80 acetonitrile and 2.5 mol/L phosphate buffer pH 6.8 16 kV. Fig. 6.2. Electrochromatographic separation of benzyl alcohol (1), resorcinol (2), methylparaben (3), and p-naphthol (4) using a soft gel column (Reprinted with permission from [27], Copyright 1998 Wiley-VCH). Conditions Column 48.5 cm (24 cm active) x 75 pm i.d., stationary phase 4.1% T, 9.7% C, 0.7% S poly(2-acrylamido-2-methyl-l-propanesulfonic acid-co-N-isopropyl acrylamide-co-methylene bisacrylamide) mobile phase 20 80 acetonitrile and 2.5 mol/L phosphate buffer pH 6.8 16 kV.
Fig. 6.21. Electrochromatographic separation of benzene derivatives on monolithic capillary column prepared by UV initiated polymerization. Conditions capillary column, 100 pm i.d. x 25 cm active length stationary phase poly(butyl methacrylate-co-ethylene dimethaciylate) with 0.3 wt. % 2-acrylamido-2-methyl-l-propanesulfonic acid pore size, 296 nm mobile phase, 75 25 vol./vol mixture of acetonitrile and 5 mmol/L phosphate buffer pH 7 UV detection at 215 nm 25 kV pressure in vials, 0.2 MPa injection, 5 kV for 3 s. Peaks thiourea (1), benzyl alcohol (2), benzaldehyde (3), benzene (4), toluene (5), ethylbenzene (6), propylbenzene (7), butylbenzene (8), and amylbenzene (9). Fig. 6.21. Electrochromatographic separation of benzene derivatives on monolithic capillary column prepared by UV initiated polymerization. Conditions capillary column, 100 pm i.d. x 25 cm active length stationary phase poly(butyl methacrylate-co-ethylene dimethaciylate) with 0.3 wt. % 2-acrylamido-2-methyl-l-propanesulfonic acid pore size, 296 nm mobile phase, 75 25 vol./vol mixture of acetonitrile and 5 mmol/L phosphate buffer pH 7 UV detection at 215 nm 25 kV pressure in vials, 0.2 MPa injection, 5 kV for 3 s. Peaks thiourea (1), benzyl alcohol (2), benzaldehyde (3), benzene (4), toluene (5), ethylbenzene (6), propylbenzene (7), butylbenzene (8), and amylbenzene (9).
Fig. 6.33. Scanning electron micrograph of a capillary column packed with 5 pm ODS silica beads and entrapped in porous poly(methyl methacrylate-co-ethylene dimethacrylate-co-2-acrylamido-2-methyl-l-propanesulfonic acid). (Reprinted with permission from [63]. Copyright 2000 American Chemical Society). Fig. 6.33. Scanning electron micrograph of a capillary column packed with 5 pm ODS silica beads and entrapped in porous poly(methyl methacrylate-co-ethylene dimethacrylate-co-2-acrylamido-2-methyl-l-propanesulfonic acid). (Reprinted with permission from [63]. Copyright 2000 American Chemical Society).
Polyaromatic hydrocarbons (naphthalene, fluorene, phen-anthrene, pyrene, benz[a]anthracene Linear polymer coated capillary [poly(N-tert.-butyl acrylamide-co-2-acrylamido-2-methyl-1 -propanesulfonic acid] Acetonitrile-50 mA/Tris buffer, pH 7.3 (30 70) 600 mm x 25 pm i.d. 450 mm effective column length 11... [Pg.387]

Linear polymer coated capillary [poly(N-tert.-butyl acrylamide-co-2-acrylamido-2-methy 1-1 -propanesulfonic acid]... [Pg.392]

Fig. 2 Response of various PECs (first polyelectrolytes in initial solutions) to subsequent addition of salt a particle mass Mw b particle radius am (corrected for polydispersity, obeying the relation Mw=(4/r/3) p am3), c structure density p 1( ) - NaPSS/PDADMAC, X=0.3, 2(0) - NaPSS/PDADMAC, X=0.6, 3(B) - DADMAC-acrylamide copolymer (47 mol% DADMAC)/NaPMA X=0.6, 4(V) - DHP2 (block copolymer of poly(2-acry-lamido-2-methyl-1-propanesulfonic acid) and poly(ethylene glycol), PEG block length 10 kda)/PDADMAC, X=0.6,1-4 addition of NaCl, 5(A) - DADMAC-acrylamide copolymer (47 mol% DADMAC)/Na-PMA, X=0.6, addition of CaCl2... Fig. 2 Response of various PECs (first polyelectrolytes in initial solutions) to subsequent addition of salt a particle mass Mw b particle radius am (corrected for polydispersity, obeying the relation Mw=(4/r/3) p am3), c structure density p 1( ) - NaPSS/PDADMAC, X=0.3, 2(0) - NaPSS/PDADMAC, X=0.6, 3(B) - DADMAC-acrylamide copolymer (47 mol% DADMAC)/NaPMA X=0.6, 4(V) - DHP2 (block copolymer of poly(2-acry-lamido-2-methyl-1-propanesulfonic acid) and poly(ethylene glycol), PEG block length 10 kda)/PDADMAC, X=0.6,1-4 addition of NaCl, 5(A) - DADMAC-acrylamide copolymer (47 mol% DADMAC)/Na-PMA, X=0.6, addition of CaCl2...
Electron hole transport composites consisting of poly(aniline-co-2-acrylami-do-2-methyl-propanesulfonic acid), (V), and silicon nanoparticles were prepared by Hsu [4] and then used to prepare light-emitting diodes and electrodes for thin film field effect transistors. [Pg.146]

Qnaternized polyW-[3-(dimethylamino)propyl]acrylamide chloride Poly[3-dimethyl(methacryloyloxyethyl)ammoninm propanesulfonate] Poly(ethylene glycol)... [Pg.159]

Polybetaine-based materials [291] and polybetaines grafted (or adsorbed) onto an inorganic particle surface are applicable as a stationary phase for ion chromatography [292]. The separation capability of poly[3-diethyl(methyl-methacryloylethyl)ammonium propanesulfonate] (polyDMAPS) grafted to silica gel and physically adsorbed onto silica gel was compared with respect... [Pg.214]

Viklund C, Svec F, Frechet JMJ, and Irgum K. Fast ion-exchange HPLC of proteins using porous poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoliths grafted with poly(2-acrylamido-2-methyl-l-propanesulfonic acid). Biotechnol. Prog. 1997 13 597. [Pg.60]

LPEI) Polyaniline (PANI) PEDOT PSS PANI poly(2-acrylamido-methane-2-propanesulfonic acid) PAMPS [196]... [Pg.98]

WSP used in this work were 2.5% w/v aqueous solution of poly (2-acrylamido-2-methyl-l-propanesulfonic acid) (poly-AMPS) for cation separations and 5% w/v solution of poly(ethylenimine) (PEI) for anion separations. [Pg.314]

Monomers 4VP, 4-vinylpyridine NIPAAm, jV-isopropylacrylamidc AA, acrylic acid PEGMA, poly (ethylene glycol) methacrylate SPE, MAI-dimethyl-AW2-methacryloyloxycthyl-/V-0-sulfopropyl)amm<>-nium betaine AMPS, 2-acrylamido-2-methyl-l-propanesulfonic acid qDMAEMA, quaternary 2-dimethylaminoethyl methacrylate St, styrene HEMA, 2-hydroxyethyl methacrylate HEA, 2-hydro-xyethyl acrylate DMAEMA, 2-dimethylaminoethyl methacrylate MAA, methacrylicacid NaSS sodium p-styrene sulfonate AC, [(2-acryloyloxy)ethyl]trimethyl ammonium chloride GMA, glycidyl methacrylate NVP, jV-vinylpyrrolidone MAn, maleic anhydride BVE n-butyl vinyl ether AAm, acrylamide DEAAm, MA-diethylacrylamidc DMAAm, MA -dimethylacrylamidc MMA, methyl methacrylate. [Pg.532]

Typical polymeric pseudostationary phases include micelle polymers, polymeric surfactants, water-soluble anionic siloxanes and dendrimers [223-231]. Micelle polymers [e.g. poly(sodium 10-undecylenate), poly (sodium 10-undecenylsulfate), poly(sodium undeconylvalinate), etc.] are synthesized from polymerizable surfactant monomers at a concentration above their critical micelle concentration. These polymers have similar structures to micelles without the dynamic nature of the micelle structure. Polymeric surfactants are polymers with surfactant properties [e.g. acrylate copolymers, such as 2-acrylamide-2-methyl-l-propanesulfonic acid and alkyl methacrylamide, alkyl methacrylate or alkyl acrylate, poly (ally lamine)-supported phases, poly(ethyleneimine), etc]. Water-soluble anionic siloxane polymers are copolymers of alkylmethylsiloxane... [Pg.656]


See other pages where Poly propanesulfonate is mentioned: [Pg.402]    [Pg.722]    [Pg.150]    [Pg.99]    [Pg.119]    [Pg.9]    [Pg.286]    [Pg.188]    [Pg.190]    [Pg.38]    [Pg.56]    [Pg.171]    [Pg.186]    [Pg.134]    [Pg.359]    [Pg.154]    [Pg.196]    [Pg.462]    [Pg.328]    [Pg.667]    [Pg.257]    [Pg.132]    [Pg.141]   
See also in sourсe #XX -- [ Pg.55 ]

See also in sourсe #XX -- [ Pg.834 ]




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3- propanesulfonate

3- propanesulfonates

Poly propanesulfonate synthesis

Poly(2-acrylamido-methane-2-propanesulfonic

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