ライフサイエンスコーパス: organic phase

1 he aqueous phase) on isoamyl nitrite (in the organic phase).

2 t Nile Red becomes chemically "gated" in the organic phase.

3 dynamic barrier for the salt transfer to the organic phase.

4 cid-insoluble carbonate or a more refractory organic phase.

5 n of metal cations by the surfactants in the organic phase.

6 l and creating water-in-oil emulsions in the organic phase.

7 tion subsequently occurs entirely within the organic phase.

8 issipation in the interfacial portion of the organic phase.

9 complex in the aqueous phase and ANE in the organic phase.

10 ol in single water droplets dispersed in the organic phase.

11 approximately 59% of the uranyl ion into the organic phase.

12 nsfer catalyst" to bring silver ion into the organic phase.

13 ain either in the interphase or in the lower organic phase.

14 or of water monomers that penetrate into the organic phase.

15 es from the droplet slowly dissolve into the organic phase.

16 lorate or phosphate) from the water into the organic phase.

17 than expected diffusion coefficients for the organic phase.

18 to buffer the activity of protons within the organic phase.

19 rate and the degree of convection within the organic phase.

20 ion could be resolved with a high content of organic phase.

21 ution of model basic drugs among aqueous and organic phases.

22 ts of organic substances between aqueous and organic phases.

23 sulfur isotopic compositions in sulfide and organic phases.

24 s controlled by manipulating the aqueous and organic phases.

25 ine B from an aqueous phase (DI water) to an organic phase (1-octanol) were performed to determine th

26 tract hydrocarbon reaction products into the organic phase after a suitable incubation period, was de

27 phobic species dissolved or suspended in the organic phase along with the amphiphilic copolymer can b

28 s phase, whereas isoamyl alcohol forms a new organic phase along with the unreacted isoamyl nitrite.

29 By using 5 mM crown ether in the organic phase and 10 mM CsNO3 with 0.1 mM HNO3 in the aq

30 , and fluorous molecules partition out of an organic phase and into a fluorous phase in a standard li

31 using UHPLC-MS purity grade methanol as both organic phase and postcolumn modifier.

32 ological samples is to partition CoQ into an organic phase and separate it from contaminants by high-

33 ith the hydrophobic side oriented toward the organic phase and the hydrophilic side toward the water.

34 d transfers of potassium between aqueous and organic phases and complexation of potassium with dibenz

35 related with an increase in transport of the organic-phase anion tetraphenylborate, TPB-, and an incr

36 fers of hydrophilic ions between aqueous and organic phases are ubiquitous in biological and technolo

37 able to extract NH4NO3 from an aqueous to an organic phase, as inferred from (1)H NMR spectroscopic a

38 l4 ](-) ions through hydrogen bonding in the organic phase, as shown by EXAFS, mass spectrometry meas

39 uch as extractions of sugars from water into organic phase, as well as in homogeneous organic media,

40 form hydroxide ion bridged dimers within the organic phases, as indicated by a significant blue shift

41 how water structures and penetrates into the organic phase at two different liquid-liquid systems: th

42 pically pass with difficulty from water into organic phases because of water's superior solvation pow

43 e extracted from an aqueous solution into an organic phase by all of the perfluoroalkylated macrocycl

44 their rapid phase transfer to a butanol/TCE organic phase can be achieved by adding NaCl and creatin

45 a combination of photo-switching dopants and organic phase-change materials as a way to introduce an

46 The sedimented organic phase (chloroform) were analysed directly by GC-

47 for Pd-NZVI reacted with TCE in the butanol organic phase compared to Fe(II) oxides in the aqueous p

48 r mole of Fe(0)) from Pd-NZVI in the butanol organic phase compared to the same reaction with TCE in

49 onally, titration of active phenoxide in the organic phase confirmed the presence of both phenol and

50 ent and a weak carboxylic acid buffer and an organic phase containing an acidic organophosphorus extr

51 Repeated washing of the organic phase containing the 212Pb@C60 malonic esters wi

52 articles were homogeneously dispersed in the organic phase containing trimesoyl chloride prior to the

53 tic boundary between an aqueous phase and an organic phase, control was achieved on the micrometer to

54 s and the strongest four components from the organic phase, country of origin was correctly identifie

55 Here, we report an organic-phase coupling strategy for nucleic acid modific

56 s and the strongest four components from the organic phase, designed to classify according to species

57 tivity, and influence of sample stirring and organic-phase diffusion coefficient on the response char

58 iquid generates carbene that migrates to the organic phase effecting living ROP.

59 by using the surfactant as the anion in the organic phase electrolyte salt.

60 detector and accompanying flow cell for the organic phase enriched with the reaction product and (b)

61 ol, and other, nonaqueous phases (gas phase, organic phase, etc.).

62 e liquid chromatography fractionation of the organic phase extract, the PQH2 content was quantitative

63 t is based on extraction into 'aqueous' and 'organic' phases for polar and nonpolar metabolites.

64 their isoelectric points, into an immiscible organic phase from an aqueous solution.

65 ploration of its reactivity in the condensed organic phase has been hampered by the lack of an approp

66 he supporting electrolyte in the aqueous and organic phases has been used to explain the shift.

67 The organic phase, however, still displays optical activity.

68 Aqueous and organic phases in microelectromembrane extraction (mu-EM

69 Continuous flow of the organic phase increases the interfacial contact with the

70 mbined with conversion of the self-assembled organic phase into inorganic replicas.

71 abel an organic-in-water emulsion, where the organic phase is an ionic liquid [P6,6,6,14][FAP]/toluen

72 The product-enriched organic phase is then sampled in an automated fashion an

73 MF product is continuously extracted into an organic phase (methylisobutylketone) modified with 2-but

74 Regarding the organic phase of bone, the hydroxyproline-to-proline rat

75 One of the most common combinations for the organic phase of dental restorative materials is BisGMA

76 a useful technology for imaging mineral and organic phases of bones and for assessing their spatial

77 The mineral and organic phases of mineralized dentin contribute co-opera

78 s, where large diffusion coefficients in the organic phase often lead to substantial sample depletion

79 The impact of surfactant addition to the organic phase on the electroactivity of proteins at the

80 iple interfaces due to internal aqueous- and organic-phase partitioning.

81 he dispersive solvent, proportion of aqueous/organic phase, pH and flow rates have been carefully eva

82 "dangling") OH group that protrudes into the organic phase, plays a key role in catalyzing reactions

83 ctions, and evaporative concentration of the organic phase prior to gas chromatography-mass spectrome

84 f dilauroylphosphatidylcholine (DLPC) to the organic phase produces an interface dominated by DLPC ad

85 tammogram of the O2(-) anion transfer to the organic phase provides a unique signature for unambiguou

86 ic compounds partition preferentially to the organic phase rather than the aqueous phase for the stud

87 ential electroosmotic pumping of aqueous and organic phase, respectively, from the solvent reservoirs

88 o monitor the partitioning between glass and organic phase, respectively.

89 simulate absorption into the above-mentioned organic phases, respectively, whereas soot, ammonium sul

90 ctions between these water molecules and the organic phase result in substantial orientation of these

91 This single-step organic phase separation is faster, more sensitive and m

92 Both the aqueous and organic phases show optical activity of near mirror imag

93 SOA formation is less sensitive than that of organic-phase SOA to atmospheric conditions that are not

94 UV-visible spectrophotometry of organic-phase solutions and thin plasticized PVC films c

95 erves as a semiseparation dimension using an organic-phase step-elution gradient in combination with

96 irmed by the fact that an immobile condensed organic phase such as PVC was protected from the photoca

97 We focus on the organic phase syntheses of magnetic NPs with precise con

98 ed by stirring, control of water activity in organic phase systems or waste biotreatment.

99 er affinity for the nonpolar interlayer DODA organic phase than for octanol.

100 nalyte from aqueous sample droplets into the organic phase that contains the sensor particles.

101 A nanopipette filled with an organic phase that is immiscible with the external aqueo

102 ring directly the transfer of nitrate to the organic phase, the enhancement of transfer of the cation

103 eriments, when the volume ratio of insoluble organic phase to aqueous one was 2:1 and the reaction te

104 can be extracted from the dendrimer into an organic phase using different surfactants.

105 ation rate (kobs of 0.413 day(-1) in butanol organic phase versus 0.099 day(-1) in aqueous phase).

106 rged intermediates from the interface to the organic phase via favorable partitioning of hydrophilic/

107 The resulting metal-organic phase was anticipated to be of the general formu

108 LLE using dichloromethane as organic phase was combined with the detection in order t

109 of the tetraalkylammonium phenoxides in the organic phase was identified as the primary factor influ

110 However, no diffusion into the organic phase was observed when [P(2)W(18)O(62)](6-) was

111 The sedimented organic phase was obtained after centrifugation, withdra

112 The organic phase was placed on the hydrophobic side of the

113 ted geometric mean concentrations during the organic phase were generally lower for all children, and

114 erally leads to dissociated complexes in the organic phase when used as a diluent in extraction studi

115 tract peptides from aqueous solution into an organic phase, where the peptides bind to the interior f

116 croemulsion droplets that then formed in the organic phase, while the high MW target protein was excl

117 d-NZVI) when reacted with TCE in a 1-butanol organic phase with limited amounts of water results in 5