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Dive into the research topics where Masanobu Sagisaka is active.

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Featured researches published by Masanobu Sagisaka.


Langmuir | 2010

Universal Surfactant for Water, Oils, and CO2

Azmi Mohamed; Kieran Trickett; Swee Yee Chin; Stephen Cummings; Masanobu Sagisaka; Laura Hudson; Sandrine Nave; Robert Dyer; Sarah E. Rogers; Richard K. Heenan; Julian Eastoe

A trichain anionic surfactant sodium 1,4-bis(neopentyloxy)-3-(neopentyloxycarbonyl)-1,4-dioxobutane-2-sulfonate (TC14) is shown to aggregate in three different types of solvent: water, heptane, and liquid CO(2). Small-angle neutron scattering (SANS) has been used to characterize the surfactant aggregates in water, heptane, and dense CO(2). Surface tension measurements, and analyses, show that the addition of a third branched chain to the surfactant structural template is critical for sufficiently lowering the surface energy, tipping the balance between a CO(2)-incompatible surfactant (AOT) and CO(2)-philic compounds that will aggregate to form micelles in dense CO(2) (TC14). These results highlight TC14 as one of the most adaptable and useful surfactants discovered to date, being compatible with a wide range of solvent types from high dielectric polar solvent water to alkanes with low dielectrics and even being active in the uncooperative and challenging solvent environment of liquid CO(2).


Journal of Colloid and Interface Science | 2015

Enhanced dispersion of multiwall carbon nanotubes in natural rubber latex nanocomposites by surfactants bearing phenyl groups

Azmi Mohamed; Argo Khoirul Anas; Suriani Abu Bakar; Tretya Ardyani; Wan Manshol bin W. Zin; Sofian Ibrahim; Masanobu Sagisaka; Paul Brown; Julian Eastoe

Here is presented a systematic study of the dispersibility of multiwall carbon nanotubes (MWCNTs) in natural rubber latex (NR-latex) assisted by a series of single-, double-, and triple-sulfosuccinate anionic surfactants containing phenyl ring moieties. Optical polarising microscopy, field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and Raman spectroscopy have been performed to obtain the dispersion-level profiles of the MWCNTs in the nanocomposites. Interestingly, a triple-chain, phenyl-containing surfactant, namely sodium 1,5-dioxo-1,5-bis(3-phenylpropoxy)-3-((3-phenylpropoxy)carbonyl) pentane-2-sulfonate (TCPh), has a greater capacity the stabilisation of MWCNTs than a commercially available single-chain sodium dodecylbenzenesulfonate (SDBS) surfactant. TCPh provides significant enhancements in the electrical conductivity of nanocomposites, up to ∼10(-2) S cm(-1), as measured by a four-point probe instrument. These results have allowed compilation of a road map for the design of surfactant architectures capable of providing the homogeneous dispersion of MWCNTs required for the next generation of polymer-carbon-nanotube materials, specifically those used in aerospace technology.


Langmuir | 2011

Super-Efficient Surfactant for Stabilizing Water-in-Carbon Dioxide Microemulsions

Masanobu Sagisaka; Shuho Iwama; Satoshi Hasegawa; Atsushi Yoshizawa; Azmi Mohamed; Stephen Cummings; Sarah E. Rogers; Richard K. Heenan; Julian Eastoe

The fluorinated double-tailed glutarate anionic surfactant, sodium 1,5-bis[(1H,1H,2H,2H-perfluorodecyl)oxy]-1,5-dioxopentane-2-sulfonate (8FG(EO)(2)), was found to stabilize water-in-supercritical CO(2) microemulsions with high water-to-surfactant molar ratios (W(0)). Studies were carried out here to obtain detailed information on the phase stability and nanostructure of the microemulsions by using a high-pressure UV-vis dye probe and small-angle neutron scattering (SANS) measurements. The UV-vis spectra, with methyl orange as a reporter dye, indicated a maximum attainable W(0) of 60 at 45 and 75 °C, and SANS profiles indicated regular droplet swelling with a linear relationship between the water core nanodroplet radius and W(0). This represents the highest water solubilization reported to date for any water-in-CO(2) microemulsion. Further analysis of the SANS data indicated critical packing parameters for 8FG(EO)(2) at the microemulsion interface >1.34, representing approximately 1.1 times the value for common aerosol-OT in water-in-heptane microemulsions under equivalent conditions.


Langmuir | 2012

Hybrid CO2-philic surfactants with low fluorine content.

Azmi Mohamed; Masanobu Sagisaka; Martin J. Hollamby; Sarah E. Rogers; Richard K. Heenan; Robert Dyer; Julian Eastoe

The relationships between molecular architecture, aggregation, and interfacial activity of a new class of CO(2)-philic hybrid surfactants are investigated. The new hybrid surfactant CF2/AOT4 [sodium (4H,4H,5H,5H,5H-pentafluoropentyl-3,5,5-trimethyl-1-hexyl)-2-sulfosuccinate] was synthesized, having one hydrocarbon chain and one separate fluorocarbon chain. This hybrid H-F chain structure strikes a fine balance of properties, on one hand minimizing the fluorine content, while on the other maintaining a sufficient level of CO(2)-philicity. The surfactant has been investigated by a range of techniques including high-pressure phase behavior, UV-visible spectroscopy, small-angle neutron scattering (SANS), and air-water (a/w) surface tension measurements. The results advance the understanding of structure-function relationships for generating CO(2)-philic surfactants and are therefore beneficial for expanding applications of CO(2) to realize its potential using the most economic and efficient surfactants.


Langmuir | 2011

Low Fluorine Content CO2-philic Surfactants

Azmi Mohamed; Masanobu Sagisaka; Frédéric Guittard; Stephen Cummings; Alison Paul; Sarah E. Rogers; Richard K. Heenan; Robert Dyer; Julian Eastoe

The article addresses an important, and still unresolved question in the field of CO(2) science and technology: what is the minimum fluorine content necessary to obtain a CO(2)-philic surfactant? A previous publication (Langmuir 2002, 18, 3014) suggested there should be an ideal fluorination level: for optimization of possible process applications in CO(2), it is important to establish just how little F is needed to render a surfactant CO(2)-philic. Here, optimum chemical structures for water-in-CO(2) (w/c) microemulsion stabilization are identified through a systematic study of CO(2)-philic surfactant design based on dichain sulfosuccinates. High pressure small-angle neutron scattering (HP-SANS) measurements of reversed micelle formation in CO(2) show a clear relationship between F content and CO(2) compatibility of any given surfactant. Interestingly, high F content surfactants, having lower limiting aqueous surface tensions, γ(cmc), also have better performance in CO(2), as indicated by lower cloud point pressures, P(trans). The results have important implications for the rational design of CO(2)-philic surfactants helping to identify the most economic and efficient compounds for emerging CO(2) based fluid technologies.


Langmuir | 2008

Water/Supercritical CO2 Microemulsions with Mixed Surfactant Systems

Masanobu Sagisaka; Daisuke Koike; Yasuaki Mashimo; Satoshi Yoda; Yoshihiro Takebayashi; Takeshi Furuya; Atsushi Yoshizawa; Hideki Sakai; Masahiko Abe; Katsuto Otake

Phase behavior was investigated for water/supercritical CO 2 (W/scCO2) microemulsions stabilized with sodium bis(1H,1H,2H,2H-heptadecafluorodecyl)-2-sulfosuccinate (8FS(EO) 2) mixed with various guest surfactants. Only for the mixtures with fluorocarbon-hydrocarbon hybrid anionic surfactants (FC6-HC n), the maximum water-to-surfactant molar ratio (W0(c)) was larger than that estimated from linear interpolation of the W0(c) values for pure 8FS(EO) 2 and pure guest surfactant. Fourier transform infrared (FT-IR) measurement for the microemulsion revealed that the mixing of 8FS(EO) 2 with FC6-HC n can prevent a phase transition from the microemulsion to the liquid crystal even in the presence of excess water. It was also found from the measurement of water/scCO 2 interfacial tension that the area occupied per surfactant molecule was markedly increased by the mixing with FC6-HC n. The loose molecular packing, probably due to a microsegregation of 8FS(EO) 2 and FC6-HC n, is consistent with the enhanced stability of the microemulsion upon surfactant mixing.


Journal of Physical Chemistry B | 2008

Fourier transform infrared spectroscopic study of water-in-supercritical CO2 microemulsion as a function of water content.

Yoshihiro Takebayashi; Yasuaki Mashimo; Daisuke Koike; Satoshi Yoda; Takeshi Furuya; Masanobu Sagisaka; Katsuto Otake; Hideki Sakai; Masahiko Abe

Fourier transform infrared (FT-IR) spectrum of water-in-supercritical CO(2) microemulsion was measured at 60 degrees C and 30.0 MPa over a wide range of water/CO(2) ratio from 0.0 to 1.2 wt % to study the distribution of water into CO(2), interfacial area around surfactant headgroup, and core water pool. The microemulsion was stabilized by sodium bis(1H,1H,2H, 2H-heptadecafluorodecyl)-2-sulfosuccinate [8FS(EO)(2)] equimolarly mixed with sodium 1-oxo-1-[4-(tridecafluorohexyl)phenyl]-2-hexanesulfonate [FC6HC4] or with poly(ethylene glycol) 2,6,8-trimethyl-4-nonyl ether [TMN-6]. The signal area of the O-H stretching band of water suggested that the number of water molecules in the microemulsion increases linearly with the water/CO(2) ratio, except for a slow initial increase below 0.4 wt % due to a part of water dissolved in CO(2). The amount of water in CO(2) was evaluated by decomposing the bending band of water into two components, one at lower frequency ascribed to water in CO(2) and the other at higher frequency to water in the microemulsion. The decomposition confirmed that CO(2) is saturated with water at the water content of 0.4 wt %. It was also revealed, from the symmetric SO stretching frequency of the surfactant, that the sulfonate headgroup is completely hydrated at the water/CO(2) ratio of 0.4-0.5 wt %. The results demonstrated that water is introduced preferentially into CO(2) and the interfacial area at small water content, and then is loaded into the micelle core after the saturation of CO(2) with water and the full hydration of the surfactant headgroup.


Langmuir | 2012

Effective and Efficient Surfactant for CO2 Having Only Short Fluorocarbon Chains

Masanobu Sagisaka; Shuho Iwama; Atsushi Yoshizawa; Azmi Mohamed; Stephen Cummings; Julian Eastoe

A previous study (Langmuir2011, 27, 5772) found the fluorinated double-tail sulfogulutarate 8FG(EO)(2) to act as a superefficient solubilizer for water in supercritical CO(2) (W/CO(2)) microemulsions. To explore more economic CO(2)-philic surfactants with high solubilizing power as well as rapid solubilization rates, the effects of fluorocarbon chain length and linking group were examined with sodium 1,5-bis(1H,1H,2H,2H-perfluoroalkyloxy)-1,5-dioxopentane-2-sulfonates (nFG(EO)(2), fluorocarbon chain length n = 4, 6, 8) and sodium 1,4-bis(1H,1H,2H,2H-perfluoroalkyloxy)-1,4-dioxobutane-2-sulfonate (nFS(EO)(2), n = 4, 8). Visual observation and UV-vis spectral measurements with methyl orange as a reporter dye indicated a maximum water-to-surfactant molar ratio (W(0)) in the microemulsions, which was 60-80 for nFG(EO)(2) and 40-50 for nFG(EO)(2). Although it is normally expected that high solubilizing power requires long fluorocarbon surfactant chains, the shortest fluorocarbon 4FG(EO)(2) interestingly achieved the highest W(0) (80) transparent single-phase W/CO(2) microemulsion. In addition, a very rapid solubilization of loaded water into CO(2) was observed for 4FG(EO)(2) even at a high W(0) of ~80.


Journal of Physical Chemistry B | 2011

Near-infrared spectroscopic study of a water-in-supercritical CO2 microemulsion as a function of the water content.

Yoshihiro Takebayashi; Masanobu Sagisaka; Kiwamu Sue; Satoshi Yoda; Yukiya Hakuta; Takeshi Furuya

A water-in-supercritical CO(2) microemulsion is a reverse micelle encapsulating a nanometer-size water droplet dispersed in supercritical CO(2). In the microemulsion solution, water exists not only in the reverse micelle but also in the solvent CO(2). For quantitative analysis of the water distribution, near-infrared spectra of water + CO(2) and water + surfactant + CO(2) mixtures were measured over a wide range of water/CO(2) ratios from 0.1 to 1.0 wt% at 60 °C and 30.0 MPa. The stretching combination band of water was decomposed into two components, a sharp one peaked at 7194 cm(-1) assigned to monomeric water dissolved in CO(2) and a broad one around 7000 cm(-1) corresponding to aggregated water in the microemulsion. Integrated molar absorptivities of these types of water were negligibly different from each other, despite the different hydrogen-bonding environments. The spectral decomposition revealed that water is distributed mainly into CO(2) at water contents smaller than 0.5 wt% and then is introduced into the microemulsion after saturation of water in CO(2) and full hydration of the surfactant headgroup.


Colloid and Polymer Science | 2014

Preparation of multiwall carbon nanotubes (MWCNTs) stabilised by highly branched hydrocarbon surfactants and dispersed in natural rubber latex nanocomposites

Azmi Mohamed; Argo Khoirul Anas; Suriani Abu Bakar; Azira Abd. Aziz; Masanobu Sagisaka; Paul Brown; Julian Eastoe; Azlan Kamari; Norhayati Hashim; Illyas Md Isa

The performance of single-, double- and triple-chain anionic sulphosuccinate surfactants for dispersing multiwall carbon nanotubes (MWNCTs) in natural rubber latex (NR-latex) was studied using a range of techniques, including field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Raman spectroscopy. The conductivities of the nanocomposites were also investigated using four-point probe measurements. Here, MWCNTs were efficiently dispersed in NR-latex with the aid of hyperbranched tri-chain sulphosuccinate anionic surfactants, specifically sodium 1,4-bis(neopentyloxy)-3-(neopentyloxycarbonyl)-1,4-dioxobutane-2-sulphonate (TC14). This paper highlights that TC14 performs much better than that of the commercially available surfactant sodium dodecyl sulphate (SDS), demonstrating how careful consideration of surfactant architecture leads to improved dispersibility of MWCNTs in NR-latex. The results should be of significant interest for improving nanowiring applications suitable for aerospace-based technology.

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Azmi Mohamed

Sultan Idris University of Education

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Sarah E. Rogers

Rutherford Appleton Laboratory

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Katsuto Otake

National Institute of Advanced Industrial Science and Technology

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Masahiko Abe

Tokyo University of Science

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Satoshi Yoda

National Institute of Advanced Industrial Science and Technology

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Yoshihiro Takebayashi

National Institute of Advanced Industrial Science and Technology

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