ライフサイエンスコーパス: polysiloxane

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 ing between the aromatic side groups and the polysiloxane backbones at 120 degrees C-130 degrees C in

12 The polysiloxane based FAVE device is highly selective for V

13 XPL is made of a tunable polysiloxane-based material that can be engineered with

14 romatic strands that wind around the central polysiloxane bundle, forming a double helix, resulting i

15 id)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way.

16 Novel materials, such as polysiloxane, ceramics, and composites, offer improved b

17 consisting of a polar trifluoropropylmethyl polysiloxane column and a nonpolar 5% phenyl dimethyl po

18 ries-coupled ensemble of a nonpolar dimethyl polysiloxane column and a polar trifluoropropylmethyl po

19 0-m length of polar, (trifluoropropyl)methyl polysiloxane column followed by a 7.0-m length of nonpol

20 sists of a 4.5-m length of nonpolar dimethyl polysiloxane column followed by a 7.5-m length of polar

21 ensemble consists of a trifluoropropylmethyl polysiloxane column followed by a dimethyl polysiloxane

22 methyl polysiloxane and a 5% phenyl dimethyl polysiloxane column was temperature-programmed at 50 deg

23 ane column and a polar trifluoropropylmethyl polysiloxane column with independent at-column heating i

24 lowed by a 7.0-m length of nonpolar dimethyl polysiloxane column.

25 ane column and a nonpolar 5% phenyl dimethyl polysiloxane column.

26 l polysiloxane column followed by a dimethyl polysiloxane column.

27 7.5-m length of polar trifluoropropylmethyl polysiloxane column.

28 ed from 4600 to 8200 plates for the dimethyl polysiloxane columns and from 3500 to 5500 plates for th

29 d the poly(ethylene glycol) and dicyanoallyl polysiloxane columns showed excessive deterioration in a

30 imethyl polysiloxane and the trifluoropropyl polysiloxane columns showed good efficiency and no signi

31 ne and the 50% cycanopropylphenyl-50% methyl polysiloxane columns showed poorer efficiency, and the p

32 to 5500 plates for the trifluoropropylmethyl polysiloxane columns.

33 a 0.5-microm-thick film of nonpolar dimethyl polysiloxane coupled in series to a polar column, either

34 and processing, which allows functionalized polysiloxane derivatives to be fabricated into 3D micros

35 ents, demonstrated unequivocally the role of polysiloxane-encapsulated "Pd"-nanoclusters as the real

36 Polysiloxane-encapsulated "Pd"-nanoclusters were generat

37 rical surfactant micelles with thin tubes of polysiloxane-forming gel networks and, upon replacing su

38 alytes compared to a commercial methylphenyl polysiloxane GLC stationary phase.

39 Amphiphilic polysiloxane graft copolymers (APGCs) were used as a del

40 Using vinyl polysiloxane impression materials and improved dental st

41 5-microm film of polar trifluoropropylmethyl polysiloxane is operated with atmospheric pressure air a

42 silyl protection for catechol-functionalized polysiloxanes is demonstrated and represents a promising

43 5))(3) to the fabrication of thin films of a polysiloxane material.

44 A lipophilic polysiloxane membrane is selectively permeable to volati

45 Elastomeric polysiloxane nanocomposites with elongations of >5000% (

46 ane, poly(ethylene glycol), and dicyanoallyl polysiloxane (nonbonded).

47 groups and groups interacting via H-bridges) polysiloxanes on thickness-shear mode resonators.

48 polysiloxane and 7.5-m trifluoropropylmethyl polysiloxane operated at an outlet pressure of 0.5 atm p

49 used to deposit a film of nonpolar dimethyl polysiloxane or moderately polar trifluoropropylmethyl p

50 a polar column, either trifluoropropylmethyl polysiloxane or poly(ethylene glycol).

51 e wash waters, including cyclic and branched polysiloxanes or polyimides, which were generated by the

52 e wash waters, including cyclic and branched polysiloxanes or polyimides, which were generated by the

53 nyl-50% methyl polysiloxane, trifluoropropyl polysiloxane, poly(ethylene glycol), and dicyanoallyl po

54 as achieved by in-situ- or ex-situ-generated polysiloxane-stabilized "Pd"-nanoclusters under mild rea

55 to prepare a nonpolar column with a dimethyl polysiloxane stationary phase and a moderately polar col

56 A 0.1-0.2-mum-thick film of dimethyl polysiloxane stationary phase is deposited on the channe

57 tography utilizing a methylated cyclodextrin/polysiloxane stationary phase is presented for the first

58 th a Pyrex wafer, and coated with a dimethyl polysiloxane stationary phase is used for the GC separat

59 ly polar column with a trifluoropropylmethyl polysiloxane stationary phase.

60 ne or moderately polar trifluoropropylmethyl polysiloxane stationary phase.

61 both ionic liquids and a popular commercial polysiloxane stationary phase.

62 Twenty subjects had polysiloxane stents fabricated with openings to permit p

63 ysiloxane, 50% cycanopropylphenyl-50% methyl polysiloxane, trifluoropropyl polysiloxane, poly(ethylen

64 loxane and dimethyl (50% liquid crystalline) polysiloxane] were compared, and retention indexes (RI)