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1 x wafer, and statically coated with dimethyl polysiloxane.
2 butes to retention more than the bulk liquid polysiloxane.
3               Fractionation of polydispersed polysiloxanes (1-2 g) into narrow molecular weight fract
4  dimethylpolysiloxane, 50% phenyl-50% methyl polysiloxane, 50% cycanopropylphenyl-50% methyl polysilo
5 column ensemble consisting of 4.5-m dimethyl polysiloxane and 7.5-m trifluoropropylmethyl polysiloxan
6  of 7.0-m lengths of a trifluoropropylmethyl polysiloxane and a 5% phenyl dimethyl polysiloxane colum
7 ents and the analyte equilibrium between the polysiloxane and cyclodextrin pseudophase.
8                    The 50% phenyl-50% methyl polysiloxane and the 50% cycanopropylphenyl-50% methyl p
9 sing a 0.50-microm film of nonpolar dimethyl polysiloxane and the second using a 0.25-microm film of
10                                 The dimethyl polysiloxane and the trifluoropropyl polysiloxane column
11                                          The polysiloxane based FAVE device is highly selective for V
12                     XPL is made of a tunable polysiloxane-based material that can be engineered with
13 id)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way.
14  consisting of a polar trifluoropropylmethyl polysiloxane column and a nonpolar 5% phenyl dimethyl po
15 ries-coupled ensemble of a nonpolar dimethyl polysiloxane column and a polar trifluoropropylmethyl po
16 0-m length of polar, (trifluoropropyl)methyl polysiloxane column followed by a 7.0-m length of nonpol
17 sists of a 4.5-m length of nonpolar dimethyl polysiloxane column followed by a 7.5-m length of polar
18 ensemble consists of a trifluoropropylmethyl polysiloxane column followed by a dimethyl polysiloxane
19 methyl polysiloxane and a 5% phenyl dimethyl polysiloxane column was temperature-programmed at 50 deg
20 ane column and a polar trifluoropropylmethyl polysiloxane column with independent at-column heating i
21 lowed by a 7.0-m length of nonpolar dimethyl polysiloxane column.
22 ane column and a nonpolar 5% phenyl dimethyl polysiloxane column.
23 l polysiloxane column followed by a dimethyl polysiloxane column.
24  7.5-m length of polar trifluoropropylmethyl polysiloxane column.
25 ed from 4600 to 8200 plates for the dimethyl polysiloxane columns and from 3500 to 5500 plates for th
26 d the poly(ethylene glycol) and dicyanoallyl polysiloxane columns showed excessive deterioration in a
27 imethyl polysiloxane and the trifluoropropyl polysiloxane columns showed good efficiency and no signi
28 ne and the 50% cycanopropylphenyl-50% methyl polysiloxane columns showed poorer efficiency, and the p
29 to 5500 plates for the trifluoropropylmethyl polysiloxane columns.
30 a 0.5-microm-thick film of nonpolar dimethyl polysiloxane coupled in series to a polar column, either
31  and processing, which allows functionalized polysiloxane derivatives to be fabricated into 3D micros
32 ents, demonstrated unequivocally the role of polysiloxane-encapsulated "Pd"-nanoclusters as the real
33                                              Polysiloxane-encapsulated "Pd"-nanoclusters were generat
34 alytes compared to a commercial methylphenyl polysiloxane GLC stationary phase.
35                                  Amphiphilic polysiloxane graft copolymers (APGCs) were used as a del
36                                  Using vinyl polysiloxane impression materials and improved dental st
37 5-microm film of polar trifluoropropylmethyl polysiloxane is operated with atmospheric pressure air a
38 silyl protection for catechol-functionalized polysiloxanes is demonstrated and represents a promising
39 5))(3) to the fabrication of thin films of a polysiloxane material.
40                                 A lipophilic polysiloxane membrane is selectively permeable to volati
41                                  Elastomeric polysiloxane nanocomposites with elongations of >5000% (
42 ane, poly(ethylene glycol), and dicyanoallyl polysiloxane (nonbonded).
43 groups and groups interacting via H-bridges) polysiloxanes on thickness-shear mode resonators.
44 polysiloxane and 7.5-m trifluoropropylmethyl polysiloxane operated at an outlet pressure of 0.5 atm p
45  used to deposit a film of nonpolar dimethyl polysiloxane or moderately polar trifluoropropylmethyl p
46 a polar column, either trifluoropropylmethyl polysiloxane or poly(ethylene glycol).
47 nyl-50% methyl polysiloxane, trifluoropropyl polysiloxane, poly(ethylene glycol), and dicyanoallyl po
48 as achieved by in-situ- or ex-situ-generated polysiloxane-stabilized "Pd"-nanoclusters under mild rea
49 to prepare a nonpolar column with a dimethyl polysiloxane stationary phase and a moderately polar col
50         A 0.1-0.2-mum-thick film of dimethyl polysiloxane stationary phase is deposited on the channe
51 tography utilizing a methylated cyclodextrin/polysiloxane stationary phase is presented for the first
52 th a Pyrex wafer, and coated with a dimethyl polysiloxane stationary phase is used for the GC separat
53 ly polar column with a trifluoropropylmethyl polysiloxane stationary phase.
54 ne or moderately polar trifluoropropylmethyl polysiloxane stationary phase.
55  both ionic liquids and a popular commercial polysiloxane stationary phase.
56                          Twenty subjects had polysiloxane stents fabricated with openings to permit p
57 ysiloxane, 50% cycanopropylphenyl-50% methyl polysiloxane, trifluoropropyl polysiloxane, poly(ethylen
58 loxane and dimethyl (50% liquid crystalline) polysiloxane] were compared, and retention indexes (RI)

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