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 es from the droplet slowly dissolve into the organic phase.

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

4 than expected diffusion coefficients for the organic phase.

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

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

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

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

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

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

11 face, but have not yet been dispersed in the organic phase.

12 on process that favors Hf extraction into an organic phase.

13 explain selective extraction of Hf into the organic phase.

14 l acid and anion-predominantly reside in the organic phase.

15 nic partitioning between the precipitate and organic phase.

16 ms maintain efficient SF (190% yield) in the organic phase.

17 ission from dyes dissolved in the high index organic phase.

18 y scattering (SAXS), of both the aqueous and organic phase.

19 issipation in the interfacial portion of the organic phase.

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

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

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

23 tion subsequently occurs entirely within the organic phase.

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

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

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

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

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

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

30 ts of organic substances between aqueous and organic phases.

31 o to reversibly transfer between aqueous and organic phases.

32 sulfur isotopic compositions in sulfide and organic phases.

33 s controlled by manipulating the aqueous and organic phases.

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

35 and showed that BBOA particles comprise two organic phases (a hydrophobic and a hydrophilic phase) a

36 e wetted tips were immersed in an immiscible organic phase, acting as a filter to extract analytes pr

37 dissolution of lipophilic ionophores in the organic phase, activation of hydrated ionophores, peculi

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

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

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

41 When in contact with an organic phase, an interfacial potential is imposed by th

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

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

44 ght-generating reactions are confined to the organic phase and photopolymerization occurs in the aque

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

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

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

48 in an increased interfacial area between the organic phase and water and a diminished emission perpen

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

50 n strength, Li(+) transference number in the organic phase, and inorganic particle size are critical

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

52 mation pathway of MSCs is similar to that in organic-phase approaches.

53 d the metabolite profiles in the aqueous and organic phases are determined by using slice-selective p

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

55 ics and structures of the amphiphiles in the organic phase as they decorate the interface.

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

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

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

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

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

61 We identify a compositional gradient, from organic phases at the electrolyte interface to inorganic

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

63 uces the amine molecule diffusion toward the organic phase boundary but also increases membrane poros

64 determined not only by the solubility in an organic phase but also by other factors like cholesterol

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

66 ed, and the analytes were recovered from the organic phase by back extraction with a 4.2 mol L(-1) HN

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

68 re a substance class with great potential as organic phase change materials (PCMs).

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

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

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

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

73 lts indicated that encapsulation depended on organic phase concentration, with higher PBAT contents a

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

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

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

77 T is studied with a nanopipet filled with an organic phase containing the trifluoroacetophenone deriv

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

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

80 dose, size, zeta potential, and affinity to organic phases correlated with leaf-to-sink translocatio

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

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

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

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

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

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

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

88 These results pave the way for organic-phase enzyme mimicry in self-assembled cavities

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

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

91 rting an optically transparent submicroliter organic-phase film in a micropillar array surrounded by

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

93 cause them to separate from both aqueous and organic phases, forming a fluorous phase.

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

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

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

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

98 In the case of colouring of the organic phase, identification and quantification was car

99 1-octanol was employed as the organic phase, impregnated within the pores of the hollo

100 The organic phase in regenerated bone showed an aligned, lay

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

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

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

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

105 water drop surrounded by an asphaltene-rich organic phase is exposed to a DC uniform electric field.

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

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

108 tion of methyl tert-butyl ether (MTBE) as an organic phase not only increased the uploading of COBE b

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

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

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

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

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

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

115 electrical double layer generated at the DP/organic phase (OP) interface while replenishing the pote

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

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

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

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

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

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

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

123 Here, we identify disordered micrometer-size organic phases rather than previously reported ordered g

124 amlining the transfer of DNA from aqueous to organic phases, replete with initiators, monomers, cross

125 mic acid and ammonium acetate in aqueous and organic phase, respectively) coupled to a mixed-mode C(1

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

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

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

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

130 We present orthogonal organic phase separation (OOPS), which does not require

131 We recently developed orthogonal organic phase separation (OOPS): a quick, efficient and

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

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

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

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

136 a, validating the property estimates for the organic phase species.

137 ere attributed to fundamental changes in the organic phase state (higher RH lowered particle viscosit

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

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

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

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

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

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

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

145 Although the precipitate is soluble in the organic phase, the depletion region separates the two an

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

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

148 water will continue to be withdrawn from the organic phase to feed the aqueous precipitation process.

149 umps to concurrently deliver the aqueous and organic phases to a mixing tee and in-line phase mixer.

150 ate, we used 1 M Cyanex 572 in Shellsol D70 (organic phase) to extract Yb(3+) and Dy(3+) from a pH 2

151 ent bone components (phosphates, carbonates, organic phase), together with the apatite unit cell para

152 rly shaped morphologies, suggesting that the organic phase transitioned to semisolid or solid.

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

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

155 phase transfer from the aqueous phase to the organic phase via a single-aggregation-single pathway.

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

157 ionic synthetic dyes from the aqueous to the organic phase was achieved (R > 99.8%).

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

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

160 ing from QN transfer from the aqueous to the organic phase was equal to 0.49 uM.

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

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

163 The sedimented organic phase was obtained after centrifugation, withdra

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

165 ganic shell, whereas the polarity of the two organic phases was indistinguishable within the solvatoc

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

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

168 These complexes are extracted into the organic phase, where femtosecond structural dynamics are

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

170 ophobic OPEs are absorbed favorably into the organic phase, whereas hydrophilic OPEs preferably parti

171 to concentrations at >90% v/v of the common organic phases, which greatly decreases the amount of ca

172 ydrogen induced polarization (nhPHIP) in the organic phase while solubilizing a protein in the aqueou

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

174 ning a pen-like device containing the gelled organic phase with a paper-supported aqueous phase.

175 rrelates the solubility of a substance in an organic phase with its membrane permeability.

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

177 solved, subdroplet imaging characterized two organic phases, with one exhibiting preferential localiz