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1 ) species by a divinyl cross-linker, such as divinylbenzene.
2 uced in situ copolymerization of styrene and divinylbenzene.
3 , and N,N-dimethylacrylamide, as well as for divinylbenzene.
4 nolith was formed from a mixture of styrene, divinylbenzene, 1-dodecanol, and toluene using 2,2'-azob
5 nalytical polymer monoliths based on styrene/divinylbenzene and methacrylate chemistries utilizing co
6 acid and 1-vinylimidazole as monomers and p-divinylbenzene as cross-linker possess the highest affin
7 emonstrate the ability of sulfonated styrene-divinylbenzene based stationary phases to separate the h
8 columns and the ease with which poly(styrene/divinylbenzene)-based stationary phases can be modified
10 cificity for sn-2 arachidonyl group, styrene-divinylbenzene beads coated with 1-stearoyl-2-[14C]-arac
11 proteolytically cleaved isoforms to styrene divinylbenzene beads coated with a phospholipid monolaye
13 -glycero-3-phosphoglycerol coated on styrene-divinylbenzene beads which could be easily monitored by
14 ds formed a stable monolayer film on styrene-divinylbenzene beads with average surface packing densit
18 ray consisting of 16 monolithic poly(styrene/divinylbenzene) capillaries for the parallel multiplex a
22 nge obtained for spiked aqueous samples with divinylbenzene/Carboxen/poly(dimethylsiloxane) fiber.
23 relatively simple extraction method using a divinylbenzene/Carboxen/poly(dimethylsiloxane) SPME fibe
24 coatings based on different polymers such as divinylbenzene/carboxen/polydimethylsiloxane (DVB/Car/PD
25 nd ascorbic acid, for 60 min at 50 C using a divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PD
26 bic acid, for 60 min at 50 degrees C using a divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PD
27 lating resin, poly(N-cyclohexylacrylamide-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propanes ulfon
28 thoxyphenylamino)-2-oxoethyl methacrylate-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propanesulfoni
30 as that on a nonfunctionalized poly(styrene-divinylbenzene) column using 1-10% acetonitrile as eluen
32 solid phase extraction (SPE) with a styrene-divinylbenzene copolymer (PPL) sorbent, which has become
33 otides on an alkylated nonporous polystyrene-divinylbenzene copolymer microsphere bead column were de
34 ENVI-Chrom P, a highly cross-linked styrene-divinylbenzene copolymer, being employed as the sorbent.
36 ibrate and evaluate an existing, polystyrene-divinylbenzene copolymeric resin-based passive air sampl
39 methacrylate (EDMA) as a functional monomer, divinylbenzene (DVB) as a cross-linker, and 2,2'-azobisi
40 -co-EDMA)] monoliths containing encapsulated divinylbenzene (DVB) nanoparticles were characterized by
42 d by the carbonization of acrylonitrile (AN)/divinylbenzene (DVB) suspension porous copolymers having
43 ospheroids via single-step polymerization of divinylbenzene (DVB) using initiated chemical vapor depo
44 embedded in poly(glycidyl methacrylate (GMA)/divinylbenzene (DVB)) tip, and (iii) pure La2O3 monolith
45 s in the colloidal crystals were filled with divinylbenzene (DVB), ethyleneglycol dimethacrylate (EDM
47 on controlled polymerization of styrene and divinylbenzene from a poly(lactide) macro-chain transfer
48 lymerization of a monomeric ionic liquid and divinylbenzene in the presence of a tissue paper in auto
50 a cation exchange resin, and PPL, a styrene-divinylbenzene media, and observed little difference in
51 lamido-2-methyl-1-pro pane sulphonic acid-co divinylbenzene] (MMAD) resin as a solid-phase extraction
52 y(4-methylstyrene-co-vinylbenzyl chloride-co-divinylbenzene) monolith via a Friedel-Crafts reaction c
53 use of 20-microm-i.d. polymeric polystyrene-divinylbenzene monolithic nanocapillary columns for the
54 olution LC separations, using a poly(styrene-divinylbenzene) monolithic column, have been coupled to
55 lypeptides carried out using poly(styrene-co-divinylbenzene) monolithic columns and carbon dioxide/me
56 including pyridine, benzene, p-xylene, and p-divinylbenzene (p-DVB), are all readily adsorbed, while
57 prototype needles were initially packed with divinylbenzene particles at SGE Analytical Science for t
58 ue is demonstrated with polydimethylsiloxane-divinylbenzene (PDMS-DVB) and polyacrylate (PA) coated S
59 onditions with polydimethylsiloxane/carboxen/divinylbenzene (PDMS/CAR/DVB) fiber were 30 C, 40 min an
60 onditions with polydimethylsiloxane/carboxen/divinylbenzene (PDMS/CAR/DVB) fiber were 30 degrees C, 4
61 siloxane (CAR/PDMS) and polydimethylsiloxane/divinylbenzene (PDMS/DVB) TFME samplers were prepared us
62 imethylsiloxane (PDMS), polydimethylsiloxane/divinylbenzene (PDMS/DVB), and polyacrylate (PA) fibers.
63 g polydimethylsiloxane (PDMS, 100 mum), PDMS/divinylbenzene (PDMS/DVB), Polyacrylate (PA) and PDMS 7
64 phase microextraction (HS-SPME) with a 65 um divinylbenzene/polydimethylsiloxane (DVB/PDMS) fiber and
66 ent receiving phases: a standard polystyrene divinylbenzene polymer with a higher specific surface ar
67 tion and solid-phase extraction with styrene-divinylbenzene polymer with a proprietary nonpolar surfa
68 racteristics of the sorbent surface (styrene divinylbenzene polymer) and increased multilayer adsorpt
70 lly recyclable bentonite functionalized with divinylbenzene-polyvinyl pyridine (PVP-DVB) for Pd (II)
71 gnetic support surface was functionalized by divinylbenzene-polyvinyl pyridine (PVP-DVB) to create a
73 superior performance compared to polystyrene-divinylbenzene (PS-DVB) copolymers in aromatic nitration
74 HPLC) method using a monolithic poly(styrene-divinylbenzene) (PS-DVB) column coupled to nanoelectrosp
76 rmance of long, high-efficiency poly(styrene-divinylbenzene) (PS-DVB), 10-microm-i.d. porous layer op
78 a polymer-based aromatic phase, poly(styrene-divinylbenzene) resin (PRP-1) are very different from th
79 (SPE) cleanup employing a polymeric styrene-divinylbenzene solid sorbent to selectively purify the w
80 , we calibrated the XAD-PAS, using a styrene-divinylbenzene sorbent, through a year-long side-by-side
84 e the chemical inertness of the poly(styrene-divinylbenzene) stationary phase, the physical robustnes
85 ely prepared by functionalization of styrene-divinylbenzene (STY-DVB) beads with N-methylglucamine to
89 alladacycles were immobilized on polystyrene-divinylbenzene supports and treated with 3-aryl-2-propyn
90 pepsin immobilized onto selected polystyrene-divinylbenzene supports was used for online digestion wi