ライフサイエンスコーパス: immiscible

1 approach is demonstrated in both inorganic (immiscible alloy and eutectic alloy) and organic materia

2 Precursory work on this family of immiscible alloys has previously highlighted their therm

3 Because these lipids are immiscible and phase separate at room temperature, a nov

4 nit is filled with five consecutive plugs of immiscible aqueous and organic solutions; the aqueous sa

5 stribution of carbon nanotubes (CNTs) in two immiscible aqueous phases formed by the addition of poly

6 his polymer solution generally exists as two immiscible aqueous phases.

7 Using two immiscible aqueous polymer solutions, we generate transi

8 The bulk-immiscible AuRh/TiO2 system can serve as a model to unde

9 In contrast, immiscible binary mixture undergo a phase separation in

10 The immiscible blocks lead to aggregation in polar and nonpo

11 h interior cavities and multiple layers with immiscible boundaries, containing patterned arrangements

12 Fusion of the aqueous droplet with the immiscible boundary effectively injects the droplet cont

13 then the droplet was fluidically moved to an immiscible boundary that isolates the CE channel (50 mic

14 surfactants that spontaneously separate into immiscible but predominantly aqueous phases-offer thermo

15 f two sets of aqueous solutions in a flow of immiscible carrier fluid within PDMS and glass microflui

16 ase boundary between aqueous plugs and water-immiscible carrier fluid.

17 mixture flows as discrete droplets inside an immiscible carrier liquid, prevents fouling by isolating

18 lets (1 pL to 10 nL volumes) dispersed in an immiscible carrier oil and enables the digital manipulat

19 ispersed into nanolitre-sized droplets by an immiscible carrier oil and then these droplets are trapp

20 e microfabricated on a PDMS chip that had an immiscible carrier phase (perfluorodecalin) pumped into

21 at forms droplets from aqueous samples in an immiscible carrier phase and encodes information about s

22 quester nanoliter to picoliter samples in an immiscible carrier phase and have gained notoriety for t

23 lume droplets surrounded by a continuous and immiscible carrier phase have attracted significant rece

24 rane samples demonstrated the presence of an immiscible cholesterol domain with a unit cell periodici

25 esence of more prominent and highly ordered, immiscible cholesterol domains.

26 y of 34.0 A, consistent with the presence of immiscible cholesterol domains.

27 cles (NPs) is achieved by contacting Ag with immiscible Co NPs.

28 regates and the surrounding hydrogels as two immiscible complex fluids in the time scale comparable t

29 poly(ethylene oxide) and two hydrophobic but immiscible components (a polymeric hydrocarbon and a per

30 ll-known technique for mixing and dispersing immiscible components within a continuous liquid phase.

31 luid front morphologies emerging during slow immiscible displacement are investigated in real time by

32 d weak wet conditions, pore-scale physics of immiscible displacement under intermediate-wet condition

33 ing CO(2)-water interface instability during immiscible displacement, and their size distribution can

34 xhibited Janus-like heterostructures made of immiscible domains sharing epitaxial interfaces.

35 anic solvent across an interface between two immiscible electrolyte solutions (ITIES) and its diffusi

36 g nanopipet-supported interfaces between two immiscible electrolyte solutions (ITIES) as tips.

37 A nanoscale interface between two immiscible electrolyte solutions (ITIES) provides a uniq

38 e micropipet-supported interface between two immiscible electrolyte solutions (ITIES) to reveal the i

39 he nanopipet-supported interface between two immiscible electrolyte solutions (ITIES) were carried ou

40 as investigated at the interface between two immiscible electrolyte solutions (ITIES).

41 t arrays of nanoscale interfaces between two immiscible electrolyte solutions (ITIES).

42 , at an array of microinterfaces between two immiscible electrolyte solutions (mu-ITIES).

43 Arrays of microscale interfaces between two immiscible electrolyte solutions (muITIES) were formed u

44 d at an array of microinterfaces between two immiscible electrolyte solutions (muITIES).

45 fusion at arrayed nanointerfaces between two immiscible electrolyte solutions (nanoITIES) was achieve

46 n transfer across nanointerfaces between two immiscible electrolyte solutions (nanoITIES); (2) combin

47 ical properties of the interface between two immiscible electrolyte solutions, 1,2-dichloroethane-H2O

48 pipet-supported ITIES (interface between two immiscible electrolyte solutions, also called a liquid/l

49 ormation about electron transfer between two immiscible electrolyte solutions, but to the best of our

50 ace mimics a liquid/liquid interface between immiscible electrolyte solutions, in which the ion trans

51 e electroassisted anion transfer between two immiscible electrolyte solutions.

52 c nanoparticles at the interface between two immiscible electrolyte solutions.

53 r nanopipet-supported interfaces between two immiscible electrolyte solutions.

54 ields can be applied at the interface of two immiscible electrolytic solutions (ITIES) in an electroc

55 positional domain structures enriched in the immiscible element, and (ii) diffusion-coupled growth of

56 butanol and ethanol) between the completely immiscible extractant and aqueous phases of the bioreact

57 We have documented an LRP5-6 heteromer using immiscible filtration assisted by surface tension (IFAST

58 Using immiscible filtration assisted by surface tension (IFAST

59 Here, we use a newly described method called immiscible filtration assisted by surface tension (IFAST

60 tanding the pore-scale dynamics of two-phase immiscible fluid flow under intermediate-wet conditions.

61 to an array of preformed plugs carried by an immiscible fluid in a microchannel.

62 ive withdrawal of one fluid through a second immiscible fluid to coat small particles with polymer fi

63 erest in segmented flow reactors that use an immiscible fluid to divide the reagent phase into discre

64 are manipulated as droplets separated by an immiscible fluid, is an intriguing format for high throu

65 de aqueous droplets (plugs) surrounded by an immiscible fluid.

66 , we describe the conditions under which two immiscible fluids flow atop one another (viewed perpendi

67 of Ca, coflowing laminar streams of the two immiscible fluids formed.

68 nt factor which controls the displacement of immiscible fluids in permeable media, with far reaching

69 Wetting properties control flow of immiscible fluids in porous media and fluids distributio

70 ometry and the rheological properties of the immiscible fluids used for encapsulation within the micr

71 en streams, and (iii) segmented plug-flow of immiscible fluids within the same channel architecture.

72 ing one hydrotrope (such as ethanol) and two immiscible fluids, both being soluble in the hydrotrope

73 e need for time-intensive wash steps, use of immiscible fluids, or precise pinning geometries.

74 lament from the cusped interface between two immiscible fluids--is shown to be the precursor of air e

75 oir-on-Chip (RoC) micromodel filled with two immiscible fluids.

76 roplets carried through a microchannel by an immiscible fluorinated fluid.

77 nanoliter aqueous droplets surrounded by an immiscible fluorinated oil phase.

78 t lung, the airspace was filled with a water-immiscible fluorocarbon.

79 microfluidic system uses multiphase flows of immiscible fluorous and aqueous fluids to form plugs, wh

80 ganic liquid, such as methanol, can form two immiscible (gas and liquid) phases within a chromatograp

81 y bi-phase emulsion droplets fabricated from immiscible hydrocarbon and fluorocarbon liquids to form

82 Consequently, a variety of immiscible hydrocarbon fluids might facilitate carbon tr

83 CHOL indicate that cerebroside and CHOL are immiscible in binary mixtures at temperatures less than

84 Fluorocarbon solvents are usually immiscible in organic solutions, and fluorous molecules

85 various degrees of open-gate state, with the immiscible interface setup being in the widely open conf

86 f oppositely charged polyelectrolytes at the immiscible interface.

87 in hexane than in aqueous solution or at the immiscible interface.

88 of the interaction of protein and molecular immiscible interfaces and the design of efficient indust

89 d the principles behind even the simplest of immiscible interfaces such as those of the liquid|liquid

90 incorporate height variations to subject the immiscible interfaces to gradients of confinement.

91 A second water-immiscible ionic liquid, 1-butyl-3-methylimidazolium bis

92 x sheets with surface tension separating two immiscible, irrotational, two-dimensional ideal fluids o

93 Here we show that immiscible isobutane forms in situ from partial transfor

94 articles are coated with a binary mixture of immiscible ligands, ordered ribbon-like domains of alter

95 Micron-scale droplets isolated by an immiscible liquid can provide miniaturised reaction vess

96 e able to direct the aquaporin into specific immiscible liquid domains in giant vesicles.

97 for levitating and transporting droplets on immiscible liquid films at higher speeds than is possibl

98 ere the liquid being repelled slides over an immiscible liquid immobilized on a porous surface.

99 roplets of one liquid suspended in a second, immiscible liquid move through a microfluidic device in

100 and cholesterol form micron-scale domains of immiscible liquid phases for only a limited range of com

101 sides of the myelin bilayer form coexisting immiscible liquid phases similar to the liquid-ordered/l

102 ese mixtures produce two distinct regions of immiscible liquid phases that span all compositions stud

103 diagrams containing two distinct regions of immiscible liquid phases, whereas those with membrane-in

104 artitioning behavior of analytes between two immiscible liquid phases.

105 pin liquids to substrates, and overlaying an immiscible liquid prevents evaporation.

106 Both miscible and immiscible liquid systems have been studied.

107 described how the physical properties across immiscible liquid-liquid interfaces should converge from

108 sorbed to the liquid-disordered phase during immiscible liquid-liquid phase coexistence, and the cont

109 g ion transfers at the interface between two immiscible liquids and homogeneous reactions in solution

110 on conditions, and (iii) the presence of two immiscible liquids and the interface between them that e

111 n this way, stable liquid boundaries between immiscible liquids are possible as long as the pressures

112 and polymerizations at the interface of two immiscible liquids are reviewed.

113 ynamic modeling of Fe-O-S liquids shows that immiscible liquids can exist at outer-core pressures (13

114 of dihydrocholesterol and phospholipids form immiscible liquids in monolayer membranes at the air-wat

115 to confine and position the boundary between immiscible liquids inside microchannels leads to a broad

116 presented that exploits the interactions of immiscible liquids with a structured surface.

117 sions do in the mutual spreading behavior of immiscible liquids, among which the liquid of lower surf

118 s the properties of interfaces between three immiscible liquids, and uses fluid flow through the tube

119 e tortuous, interconnected structures of two immiscible liquids, kinetically trapped by colloidal par

120 sing segmented flow in a two-phase system of immiscible liquids, which delivers aqueous droplets into

121 ing have been compared with the behaviors of immiscible liquids, which they closely resemble.

122 conformal thin films at the interface of two immiscible liquids.

123 enabling the control of the boundary between immiscible liquids.

124 and dynamic droplets of fluids in different immiscible media have been used as individual vessels to

125 which have a lower refractive index than the immiscible medium in which the droplets are immersed and

126 complement recent experimental evidence for immiscible methane-rich fluids at 600-700 degrees C and

127 A combination of immiscible molecules in the ligand shell of a gold nanop

128 surface pressure pi of 30 mN/m, and forms an immiscible monolayer mixture with DPPC.

129 racterize colorimetric probes in other water immiscible nanomaterials.

130 collected at 7 s intervals, segmented by an immiscible oil and stored in a capillary tube.

131 ates into nanoliter droplets segmented by an immiscible oil at 4.5 samples/s and sequentially analyze

132 is of aqueous plugs segmented in a stream of immiscible oil is described.

133 Parallel sample recovery in an immiscible oil stream offers the advantage of low sample

134 mum inner diameter LC column segmented by an immiscible oil such as perfluorodecalin.

135 with a sample volume of 8 nL segmented by an immiscible oil.

136 nt freezing points for aqueous solutions and immiscible oils, we froze a stream of aqueous droplets t

137 are dehydrated at the interface between two immiscible oils.

138 ed in an array of microwells, after which an immiscible organic (phenol-chloroform) phase was introdu

139 phase at the bottom of a sample vial, via an immiscible organic filter phase, into a 2 muL acceptor p

140 lize the underwater lossless manipulation of immiscible organic liquid droplets with a large volume.

141 Not a conventional glass cuvette, but water-immiscible organic liquid, is used as the container for

142 ion to measure densities of solids and water-immiscible organic liquids with accuracies ranging from

143 e basis of their isoelectric points, into an immiscible organic phase from an aqueous solution.

144 liquid aqueous sample donor phase through an immiscible organic solvent layer acting as a filter phas

145 al library samples were dissolved in a water-immiscible organic solvent, butyl acetate, and added to

146 Then crude plasma samples and a water-immiscible organic solvent, methyl ethyl ketone, were se

147 n nanotube (SWNT) suspensions are mixed with immiscible organic solvents.

148 by reversibly penetrating and resealing the immiscible partition.

149 f the neutral assemblies formed in the water-immiscible phase are usually not well defined and the ca

150 e have investigated how lipid concentration, immiscible phase flow velocities and the device geometri

151 ements, which are highly fractionated by the immiscible phase separation that produces these carbonat

152 ay of chambers that have been primed with an immiscible phase.

153 cantly reduced by segmentation with a second immiscible phase.

154 ume aqueous droplet that is surrounded by an immiscible phase.

155 aptured on a solid phase through one or more immiscible-phase barriers that efficiently exclude the p

156 xide, helium and carbon dioxide can form two immiscible phases over extended composition ranges.

157 used referring to systems consisting of two immiscible phases, one of which is finely dispersed into

158 quid-liquid partitioning process between two immiscible phases, respectively.

159 using the liquid/liquid interfaces of three immiscible phases.

160 spherical particles can be obtained by using immiscible polymer pairs and by employing surface treatm

161 By combining three mutually immiscible polymeric components in a mixed-arm star bloc

162 ular network polymer consisting of a pair of immiscible polymers, poly(butyl)methacrylate (PBMA) and

163 cles in the presence of a small amount of an immiscible secondary liquid.

164 ur issues from a carbon anode immersed in an immiscible secondary molten salt electrolyte disposed ab

165 Block copolymers with chemically immiscible segments exhibit a variety of microphase-sepa

166 u-EME) were formed as adjacent plugs of free immiscible solutions in narrow-bore polymeric tubing, an

167 st microreactors, to extract product into an immiscible solvent during reaction, and to use Leidenfro

168 tercurrent chromatography (CCC) using solely immiscible solvent systems allowed the fractionation of

169 ng metal cations or metal salts into a water-immiscible solvent usually operate in the inner coordina

170 s, MXx(n-), or metal salts, MXx into a water-immiscible solvent.

171 The use of water-immiscible solvents is key and leads to a 1-3 orders of

172 gest retention values can be expected from W-immiscible solvents that fully remain in the bulk MP.

173 e status of these assemblies in a mixture of immiscible solvents, these dendrimers were found to be k

174 re favoured by the low polarity of the water-immiscible solvents.

175 y the photoactivated transitions between two immiscible states of the polymer.

176 imensional map that divides the miscible and immiscible systems into distinctly clustered regions.

177 The classification of miscible and immiscible systems of binary alloys plays a critical rol

178 Furthermore, the use of immiscible systems, e.g., in emulsions, offers an easy m

179 r in a phase-transfer polymerization with an immiscible THF solution of monomer and initiator.

180 binary mixtures, we investigate the miscible-immiscible transition at finite temperature by means of

181 rst of the metals in the condensed state and immiscible under normal conditions.

182 Polystyrene dissolved in a water-immiscible, volatile solvent was deposited in a humid en

183 We find that these two OA types are immiscible, which informs our inference of the morpholog

184 x is miscible with DPPC and cholesterol, and immiscible with DOPC.

185 similar hydrocarbon makeup, the polymers are immiscible with one another.

186 ite IA-2) is dissolved in an organic solvent immiscible with the aqueous eluent.

187 pipette filled with an organic phase that is immiscible with the external aqueous solution was used a

188 tum cells, rendering them distinct from, and immiscible with, neighboring wing cells.

189 These two types of bonds are intrinsically immiscible without cosolvents.