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論文

Contrast dependence of scattering profiles for poly(ethylene glycol) in water; Investigation by small-angle neutron scattering with $$^{3}$$He spin filter and small-angle X-ray scattering

領木 研之*; 渡部 史*; 奥平 琢也*; 高橋 慎吾*; 奥 隆之; 廣井 孝介; 元川 竜平; 中村 洋*

Journal of Chemical Physics, 160(11), p.114907_1 - 114907_9, 2024/03

Small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS) measurements were performed for deuterated and non-deuterated poly(ethylene glycol) (d-PEG and h-PEG, respectively) in D$$_{2}$$O and a D$$_{2}$$O/H$$_{2}$$O mixed solvent (Mix) to compere the scattering profiles. To determine the coherent scattering intensity of SANS, a $$^{3}$$He spin filter was utilized. The scattering profiles determined by SANS measurements were analyzed in terms of the wormlike chain model with touched beads along the contour of the chain. However, the SAXS profiles were not explained by the same model with uniform beads but with beads each consisting of a core and a shell having different electron densities. To explore the chain thickness determined form the SANS profile, scattering intensities for different combinations of d-PEG/D$$_{2}$$O, d-PEG/Mix, h-PEG/D$$_{2}$$O, and h-PEG/Mix were also examined.

論文

Upgrade of the small-angle neutron scattering diffractometer SANS-J at JRR-3

熊田 高之; 元川 竜平; 大場 洋次郎; 中川 洋; 関根 由莉奈; Micheau, C.; 上田 祐生; 杉田 剛; 美留町 厚; 佐々木 未来; et al.

Journal of Applied Crystallography, 56(6), p.1776 - 1783, 2023/12

 被引用回数:1 パーセンタイル:65.66(Chemistry, Multidisciplinary)

既存のメイン検出器および高位置分解能フォトマル検出器に加えて新規に導入した前面検出器を組み合わせることにより、波数0.002nm$$^{-1}$$から6nm$$^{-1}$$にわたる散乱を3つの光学機器配置により切れ目なく測定できるようになった。またグラフィカルユーザーインターフェースの導入と併せて装置のユーザビリティが大幅に向上した。

論文

Water fraction dependence of the aggregation behavior of hydrophobic fluorescent solutes in water-tetrahydrofuran

辻 勇人*; 中畑 雅樹*; 菱田 真史*; 瀬戸 秀紀*; 元川 竜平; 井上 大傑*; 江川 泰暢*

Journal of Physical Chemistry Letters (Internet), 14(49), p.11235 - 11241, 2023/12

 被引用回数:0 パーセンタイル:0.01(Chemistry, Physical)

This work investigates the water-fraction dependence of the aggregation behavior of hydrophobic solutes in water-tetrahydrofuran (THF) and the elucidation of the role of THF using fluorescence microscopy, dynamic light scattering, neutron and X-ray scattering, as well as photoluminescence measurements. Based on the obtained results, the following model is proposed: hydrophobic molecules are molecularly dispersed in the low-water-content region (10-20 vol %), while they form mesoscopic particles upon increasing the water fraction to $$sim$$30 vol percent. This abrupt change is due to the composition fluctuation of the water-THF binary system to form hydrophobic areas in THF, followed by THF-rich droplets where hydrophobic solutes are incorporated and form loose aggregates. Further increasing the water content prompts the desolvation of THF, which decreases the particle size and generates tight aggregates of solute molecules. This model is consistent with the luminescence behavior of the solutes and will be helpful to control the aggregation state of hydrophobic solutes in various applications.

論文

Structural changes of polystyrene particles in subcritical and supercritical water revealed by in situ small-angle neutron scattering

柴田 基樹*; 中西 洋平*; 阿部 淳*; 有馬 寛*; 岩瀬 裕希*; 柴山 充弘*; 元川 竜平; 熊田 高之; 高田 慎一; 山本 勝宏*; et al.

Polymer Journal, 55(11), p.1165 - 1170, 2023/11

 被引用回数:1 パーセンタイル:51.7(Polymer Science)

Marine ecosystem degradation due to micro plastics is a significant environmental problem, as acknowledged by Sustainable Development Goal 14. Decomposition of plastics using near critical or supercritical water is one of the promising methods to reduce micro plastics. To attain the optimization of the method for improving environmental friendliness, it is necessary to clarify the structural change of materials during the process. We, thus, investigated the decomposition processes of polystyrene particles dispersed in deuterated water (D$$_{2}$$O) during heating under near critical or supercritical conditions by using in situ small-angle neutron scattering. Under subcritical conditions, the PS particles were swollen by D$$_{2}$$O due to increased compatibility with temperature. Near the critical point in subcritical conditions, the cleavage of PS chains in the particles occurred, so that the swollen ratio was much enhanced though the PS particles kept their shapes. In a supercritical condition, the PS particles were degraded into oil including oligomers or monomers and the phase-separated structures with styrene-rich and D$$_{2}$$O-rich regions.

論文

Heterogeneous aggregation of humic acids studied by small-angle neutron and X-ray scattering

斉藤 拓巳*; 元川 竜平; 大窪 貴洋*; 三浦 大輔*; 熊田 高之

Environmental Science & Technology, 57(26), p.9802 - 9810, 2023/07

 被引用回数:0 パーセンタイル:0(Engineering, Environmental)

Aggregation of humic acids (HAs) were studied by small-angle neutron and X-ray scattering techniques. The combination of these techniques enables us to examine aggregation structures of heterogeneous HA particles. Two HAs with distinctive compositions were examined; a commercial HA (PAHA) and a HA extracted from deep sedimentary groundwater (HHA). While macroscopic coagulation tests showed that these HAs were stable in solutions except for HHA at pH $$<$$ 6, small-angle neutron scattering (SANS) and X-ray scattering (SAXS) revealed that they formed aggregates with the sizes exceeding sub-micrometer length scale. The SAXS curves of PAHA remarkably varied with pD, whereas the SANS curves did not. With the help of theoretical fittings, it was revealed that PAHA aggregates consisted of two domains: poorly hydrated cores and well-hydrated proton-rich shells. The cores are (dis)aggregated with pD inside the aggregates of the shell. The SANS and SAXS curves of HHA resemble each other, and their intensities at low q increased with a decrease of pD, indicating the formation of homogeneous aggregates. This study revealed that distinctive aggregation behaviors exist in humic substances with heterogeneous structures like PAHA, which is invaluable for their roles in the fate of contaminants or nutrients in aqueous environments.

論文

Foam flotation of clay particles using a bifunctional amine surfactant

Micheau, C.; 上田 祐生; 元川 竜平; Bauduin, P.*; Girard, L.*; Diat, O.*

Langmuir, 39(31), p.10965 - 10977, 2023/07

 被引用回数:0 パーセンタイル:0(Chemistry, Multidisciplinary)

Understanding clay flotation mechanisms has become a major concern because of the increasing level of environmental contamination of soil and ground water by heavy metals and radionuclides. Clays are often used as sorbents for extracting metals in indirect flotation processes but can function simultaneously as defoamers. However, how foam generation and stability depend on the molecular interactions between the clays and surfactant is still controversial. In the present study, an amine polyethoxylated surfactant was used as a bifunctional surfactant that collected clay particles and acted as a foaming agent in the flotation process. The pH conditions strongly affected the surfactant physicochemical properties, allowing the clay extraction efficiency to be tuned. The interfacial recovery factor of the clays almost reached 100 percent under acidic (pH lower than 6) and neutral (pH 6-10) conditions, whereas it was negative under alkaline conditions (pH higher than 10), contrary to expectations. To elucidate the mechanisms involved in the particle flotation process for each of the pH conditions, the bulk and foam phases were analyzed. The effects of electrostatic interactions between the solutes and multiscale structure on the clay extraction behavior were investigated by electrophoretic measurements, dynamic light scattering, small-angle neutron scattering, and image analysis. Based on these results, three flotation processes were found depending on pH range: surfactant foam fractionation at pH higher than 10; clay particle foam flotation at pH 6-10; and particle froth flotation at pH lower than 6.

論文

Microscopic structural changes during the freeze cross-linking reaction in carboxymethyl cellulose nanofiber hydrogels

三浦 大輔*; 関根 由莉奈; 南川 卓也; 杉田 剛; 大場 洋次郎; 廣井 孝介; 大澤 辰彦

Carbohydrate Polymer Technologies and Applications (Internet), 4, p.100251_1 - 100251_9, 2022/12

凍結架橋により形成されたカルボキシメチルセルロースナノファイバー(CMCF)ゲルの反応機構を調べた。異なる反応時間で調製されたCMCFヒドロゲルの物性評価により、凍結架橋反応中の階層構造変化の観察に成功した。凍結架橋CMCFヒドロゲルは、従来の方法で形成された通常のゲルとは異なり、オングストロームからマイクロメートルスケールまでの特徴的な階層構造を示し、その特異的構造が飛躍的な力学強度の向上に寄与していることを明らかにした。

論文

Polymer photonic crystals prepared by triblock copolymerization-induced ${it in situ}$ microphase separation

磯崎 祐嘉*; 東原口 誠也*; 金子 直矢*; 山崎 駿*; 谷口 竜王*; 唐津 孝*; 上田 祐生; 元川 竜平

Chemistry Letters, 51(6), p.625 - 628, 2022/06

 被引用回数:2 パーセンタイル:29.84(Chemistry, Multidisciplinary)

Polymer photonic crystals (PPCs) that selectively reflect visible light were prepared by triblock polymerization-induced ${it in situ}$ microphase separation via reversible addition-fragmentation chain transfer polymerization. The addition of homopolymer to the polymerization system swelled a specific phase of the microdomains, enabling the preparation of PPCs with long-wavelength structural colors. Small-angle neutron scattering confirmed the increase in the domain spacing of the lamellar microdomains with the addition of homopolymer, while maintaining their morphology.

論文

Polarization analysis for small-angle neutron scattering with a $$^{3}$$He spin filter at a pulsed neutron source

奥平 琢也; 上田 祐生; 廣井 孝介; 元川 竜平; 稲村 泰弘; 高田 慎一; 奥 隆之; 鈴木 淳市*; 高橋 慎吾*; 遠藤 仁*; et al.

Journal of Applied Crystallography, 54(2), p.548 - 556, 2021/04

 被引用回数:2 パーセンタイル:33.1(Chemistry, Multidisciplinary)

$$^{3}$$Heスピンフィルタを中性子スピン解析子として使用することにより、パルス中性子源での中性子小角散乱実験において、偏極解析を行うことに成功した。本実験に使用した$$^{3}$$Heスピンフィルタは中性子小角散乱実験を行うために十分な立体角をカバーすることができ、$$^{3}$$He偏極緩和時間も数日と長く、これは実験を完遂するために十分な性能である。水素原子による非干渉性散乱は非常に大きく、試料の組成から計算によって非干渉性散乱量を見積もる試みが行われていたが、正確に非干渉性散乱量を決定することは難しかった。しかし本研究では試料内での中性子の多重散乱を考慮した偏極解析実験を行うことで、干渉性散乱と非干渉性散乱を正確に分離することが可能となった。現在までパルス中性子源での中性子小角散乱では、偏極解析の手法が確立されていなかったが、本成果によって、様々な種類の試料に対して干渉性散乱と非干渉性散乱を正確に分離することができるようになると予想される。

論文

Precious metal separations

成田 弘一*; 粕谷 亮*; 鈴木 智也*; 元川 竜平; 田中 幹也*

Encyclopedia of Inorganic and Bioinorganic Chemistry (Internet), 28 Pages, 2020/12

The increasing use of precious metals (PMs) in industrial products such as electronics and catalysts has been increasingly important in PM separations. Most of PM separation and purification processes are performed using acidic chloride solutions; therefore, understanding of chemical properties and separation mechanisms of PM chloridometalates in solution is of key importance for improving the processes. This article focuses on solvent extraction of PMs from acidic chloride solutions as the main technology for the mutual separation of PMs and extensively covers the classical and modern methods. In addition, leaching methods, dominant species in acidic chloride solutions, and non-solvent extraction separation methods are also described.

論文

X-ray and neutron study on the structure of hydrous SiO$$_{2}$$ glass up to 10 GPa

浦川 啓*; 井上 徹*; 服部 高典; 佐野 亜沙美; 小原 真司*; 若林 大佑*; 佐藤 友子*; 船守 展正*; 舟越 賢一*

Minerals (Internet), 10(1), p.84_1 - 84_13, 2020/01

 被引用回数:9 パーセンタイル:64.36(Geochemistry & Geophysics)

含水SiO$$_{2}$$ガラスの構造は、酸化物ガラスやマグマの物理化学的性質に対する水の影響を調べるために基礎的な情報である。D$$_{2}$$Oを13重量%濃度含む含水SiO$$_{2}$$ガラスを、高温高圧下で合成し、その構造を小角X線散乱、X線回折、中性子回折により、室温10GPaまでの範囲で調べた。この含水ガラスはSiO$$_{2}$$が卓越した主成分とD$$_{2}$$Oが卓越した少量の成分に相分離していることが分かった。またその中距離構造は、含水化でSi-OH水酸基ができたことによりSiO$$_{4}$$連結が壊れ、無水のガラスより縮んでいた。その一方で、高圧下での挙動に違いは見られなかった。また、多くのD$$_{2}$$O分子は、小さな領域にかたまっており、その主成分であるSiO$$_{2}$$ガラス相へは侵入していないと思われる。

論文

Proton chelating ligands drive improved chemical separations for rhodium

成田 弘一*; Nicolson, R. M.*; 元川 竜平; 伊藤 文之*; 森作 員子*; 後藤 みどり*; 田中 幹也*; Heller, W. T.*; 塩飽 秀啓; 矢板 毅; et al.

Inorganic Chemistry, 58(13), p.8720 - 8734, 2019/07

 被引用回数:14 パーセンタイル:69.69(Chemistry, Inorganic & Nuclear)

Current industrial practices to extract rhodium from virgin ores carry a heavy environmental burden. Improving the efficiency of the hydrometallurgical processes to separate and recover rhodium from other precious metals provides an opportunity to improve the materials and energy balances, but the presence of mixed chloride-rhodium species following leaching by acid chloride media complicates the recovery process. In this work we have applied a broad range of analytical techniques (FT-IR spectroscopy, X-ray diffraction, EXAFS, water-transfer analysis, small-angle neutron scattering, NMR spectroscopy, and electrospray mass spectrometry), which together show that the amino-amide reagent preferentially transports chlorido-rhodium species as a 1:2 neutral assembly from aqueous 2.0 M HCl phase into an organic phase. The extractants then ligate in the outer coordination shell of the chloride-rhodium anion, making this an efficient separation process. In this study, we found that protonation to the extractants induced to form a proton chelate ring, which pre-organises the ligand to present an array of charge diffuse C-H bonds. This templated arrangement of positive dipoles favors complexation to the charge diffuse chloride-rhodium anion over the more charge-dense chloride anion.

論文

Structural approach to understanding the solubility of metal hydroxides

小林 大志*; 中嶋 翔梧*; 元川 竜平; 松村 大樹; 斉藤 拓巳*; 佐々木 隆之*

Langmuir, 35(24), p.7995 - 8006, 2019/06

 被引用回数:5 パーセンタイル:22.5(Chemistry, Multidisciplinary)

We report the hierarchical structure of zirconium hydroxide after aging at different temperatures to elucidate the factors governing zirconium solubility in aqueous solutions. Zirconium hydroxide solid phases after aging at 25, 40, 60, and 90$$^{circ}$$C under acidic to alkaline conditions were investigated using extended X-ray absorption fine structure (EXAFS) and wide- and small-angle X-ray scattering (WAXS and SAXS) techniques to reveal the bulk and surface structures of the solid phases from the nanoscale to submicroscale. After aging at 25 $$^{circ}$$C, the fundamental building unit of the solid phase was a zirconium hydroxide tetramer. The tetramers formed primary particles approximately 3 nm in size, which in turn formed aggregates hundreds of nanometers in size. This hierarchical structure was found to be stable up to 60 $$^{circ}$$C under acidic and neutral conditions and up to 40 $$^{circ}$$C under alkaline conditions. After aging at 90 $$^{circ}$$C under acidic conditions and at 60 and 90 $$^{circ}$$C under alkaline conditions, the WAXS and EXAFS measurements suggested the crystallization of the solid phase. The transformation of the solid-phase structure by temperature was discussed in relation to the solubility product to understand the solubility-limiting solid phase. The solubility of zirconium hydroxide after aging at different temperatures was governed not only by the size of the primary particles, but also by their surface configuration.

論文

A Telescoping view of solute architectures in a complex fluid system

元川 竜平; 小林 徹; 遠藤 仁; Mu, J.*; Williams, C. D.*; Masters, A. J.*; Antonio, M. R.*; Heller, W. T.*; 長尾 道弘*

ACS Central Science, 5(1), p.85 - 96, 2019/01

 被引用回数:46 パーセンタイル:86.05(Chemistry, Multidisciplinary)

We present a hierarchical aggregate model of an organic phase containing a coordination species that acts as a fundamental building unit of higher-order structures formed in the organic phase. We aimed to elucidate the fundamental aspects of the microscopic structure and phase separation occurring in ionic separation and recovery systems during solvent extraction. The coordination species aggregate through a hydrogen-bonding network formed by interaction between the hydrophilic part of the coordination species with extracted water and acid molecules. This reduces the hydrophilic surface area, resulting in subsequent formation of small primal clusters of 2 to 3 nm in diameter. The primal clusters further aggregate due to van der Waals interaction to form large aggregates of $$<$$ 10 nm in diameter. The size of the primal cluster does not depend on the concentration of the coordination species, whereas the size of the large aggregate increases as the aggregation number of the primal clusters increases. We conclude that hybrid interaction is a key driving force in the formation and growth of the hierarchical aggregate and the induction of phase separation of the organic phase.

論文

Phase-transition kinetics of magnetic skyrmions investigated by stroboscopic small-angle neutron scattering

中島 多朗*; 稲村 泰弘; 伊藤 崇芳*; 大石 一城*; 大池 広志*; 賀川 史敬*; 吉川 明子*; 田口 康二郎*; 加倉井 和久*; 十倉 好紀*; et al.

Physical Review B, 98(1), p.014424_1 - 014424_5, 2018/07

 被引用回数:7 パーセンタイル:34.59(Materials Science, Multidisciplinary)

MnSi中に発生する磁気スキルミオンの相転移の挙動を中性子小角散乱ストロボスコピック測定により観測した。温度を50K/秒という速度で急激に変化させている間に13マイクロ秒の時間分解能で中性子小角散乱パターンの時間変化を測定することに成功し、その結果、温度の上昇によって磁気スキルミオンが消滅する様子や、急速な冷却過程で生成されたスキルミオンが本来存在できない低温まで過冷却状態で残る様子などが明らかとなった。

論文

Hierarchically self-organized dissipative structures of filler particles in poly(styrene-$$ran$$-butadiene) rubbers

山口 大輔; 湯浅 毅*; 曽根 卓男*; 冨永 哲雄*; 能田 洋平*; 小泉 智*; 橋本 竹治*

Macromolecules, 50(19), p.7739 - 7759, 2017/10

 被引用回数:14 パーセンタイル:48.82(Polymer Science)

スチレン-ブタジエンランダム共重合体におけるフィラー粒子の空間分布を解明した。中性子小角散乱実験の結果、本共重合体中におけるフィラーは5つの構造レベルからなる階層構造を形成していることが判明した。

論文

溶媒抽出法による白金族金属分離に関する最近の研究

成田 弘一*; 鈴木 智也*; 元川 竜平

日本金属学会誌, 81(4), p.157 - 167, 2017/04

 被引用回数:17 パーセンタイル:62.95(Metallurgy & Metallurgical Engineering)

Most of the refineries for platinum group metals (PGMs) in Japan have adopted solvent extraction methods for mutual separation of PGMs. Few effective extractants for industrial use have been found although some industrial processes were established in 1970s. Recently, some compounds have been reported as candidates for practical PGM extractants in addition to new concepts for PGM extraction mechanisms. In this review article, we present well-known PGM recovery processes based on solvent extraction, industrial extractants and their properties, and conventional extraction mechanism for PGMs. Additionally, we discuss recent interesting extraction systems (amide-type compounds and ionic liquid) and then introduce new extraction concepts based on the specific interactions at the outer-sphere of a metal complex in the organic phase.

論文

Contrast variation by dynamic nuclear polarization and time-of-flight small-angle neutron scattering, 1; Application to industrial multi-component nanocomposites

能田 洋平*; 小泉 智*; 増井 友美*; 間下 亮*; 岸本 浩通*; 山口 大輔; 熊田 高之; 高田 慎一; 大石 一城*; 鈴木 淳市*

Journal of Applied Crystallography, 49(6), p.2036 - 2045, 2016/12

 被引用回数:19 パーセンタイル:78.58(Chemistry, Multidisciplinary)

We have reported the first attempt with dynamic nuclear polarization (DNP) and contrast variation small-angle neutron scattering (SANS) experiments on model mixtures for industrial tyres conducted at the MLF of J-PARC. We performed time-of-flight SANS (TOF-SANS) experiments, employing neutrons with a wide range, which causes imperfect neutron polarization and variations in the coherent and incoherent scattering lengths. By carefully eliminating the effect of imperfect neutron polarization, separation of the partial scattering functions was successfully demonstrated for the ternary system styrene-butadiene-rubber/silica/carbon.

論文

Nanoscopic structural investigation of physically cross-linked nanogels formed from self-associating polymers

関根 由莉奈; 遠藤 仁*; 岩瀬 裕希*; 竹田 茂生*; 向井 貞篤*; 深澤 裕; Littrell, K. C.*; 佐々木 善浩*; 秋吉 一成*

Journal of Physical Chemistry B, 120(46), p.11996 - 12002, 2016/11

 被引用回数:10 パーセンタイル:26.96(Chemistry, Physical)

コントラスト変調中性子小角散乱法を用いてコレステロール置換プルラン(CHP)が形成するナノゲルの内部微細構造の評価を行った。溶媒の重水分率の異なるCHPナノゲル水溶液の散乱強度を分離してCHPナノゲルを構成するプルラン、コレステロール、プルランーコレステロールのcross-termの部分散乱関数を求めて解析を行った。結果、プルラン鎖が形成するナノゲル骨格は半径8.1nmの大きさであった。また、CHPナノゲル内において、約3個のコレステロール分子から成る架橋点が19個形成され、フラクタル次元2.6で分布していることを明らかにした。また、架橋点と高分子鎖のcross-termを解析したところ、部分鎖の大きさは半径約1.7nmであった。以上の結果より、ナノゲルの内部微細構造を明らかにした。

論文

Small-angle neutron scattering study of specific interaction and coordination structure formed by mono-acetyl-substituted dibenzo-20-crown-6-ether and cesium ions

元川 竜平; 小林 徹; 遠藤 仁*; 池田 隆司; 矢板 毅; 鈴木 伸一; 成田 弘一*; 阿久津 和宏*; Heller, W. T.*

Journal of Nuclear Science and Technology, 53(8), p.1205 - 1211, 2016/08

 被引用回数:0 パーセンタイル:0.01(Nuclear Science & Technology)

This study uses small-angle neutron scattering (SANS) to elucidate the coordination structure of the complex of mono-acetyl substituted dibenzo-20-crown-6-ether (ace-DB20C6) with Cs. SANS profiles obtained for the complex of ace-DB20C6 and Cs (ace-DB20C6/Cs) in deuterated dimethyl sulfoxide indicated that Cs coordination resulted in a more compact structure than the free ace-DB20C6. The data were fit well with SANS profiles calculated using Debye function for scattering on an absolute scattering intensity scale. For this theoretical calculation of the scattering profiles, the coordination structure proposed based on a density functional theory calculation. Consequently, we conclude that the SANS analysis experimentally supports the proposed coordination structure of ace-DB20C6/Cs and suggests the following: (1) the complex of ace-DB20C6 and Cs is formed with an ace-DB20C6/Cs molar ratio of 1/1; (2) the two benzene rings of ace-DB20C6 fold around Cs above the center of the crown ether ring of ace-DB20C6.

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