Colloid probe investigation of the stabilization mechanism in aqueous 1,2-propanediol nano-zirconia dispersions
文献情報
P. Kuschel, A. Kristoffersson, B. Clauss, W. Oppermann, W. Sigmund
Surface forces controlling colloidal stability of nano-zirconia particles with dispersant [2-(2-(2-methoxy ethoxy) ethoxy) acedic acid-TODA] and without dispersant were investigated using the colloid probe technique in an atomic force microscope. 1,2-propanediol/water mixtures (containing 0, 25, 50, and 75 wt.% propanediol) were used as dispersing media. Hamaker constants for zirconia in these mixtures were calculated and the surface-zeta-potential determined for nano-zirconia powder in these media. Quantitative analysis of surface forces for zirconia without dispersants suggests an electrostatic stabilization mechanism. The size of the electrostatic barrier was found to be a function of the propanediol content in the medium and decreased with increasing propanediol level. Since adding 1,2-propanediol reduced the Hamaker constant A131, all investigated samples remained colloidally stable (no attraction was detected). Application of Derjaguin–Landau–Verweij–Overbeek theory (DLVO) to fitting curves strongly indicates that TODA acts mainly as a steric dispersant. An additional depletion effect is being discussed, which may contribute to the stabilization process. Further, it is suggested that TODA does not preferably adsorb onto zirconia with the carboxylic head group. Instead, a “flat” adsorption may be indicated, where the molecule forms a layer surrounding the zirconia and the oxygen groups in the backbone may interact with the OH surface sites. However, TODA may only act successfully as a dispersant, if the dispersing medium possesses a suitably small Hamaker constant. A minimum of 50% propanediol was needed to give a significant dispersing force.
関連文献
Through-space interactions between face-to-face, center-to-edge oriented arenes: importance of polar–π effects
Franco Cozzi, Rita Annunziata, Maurizio Benaglia, Mauro Cinquini, Laura Raimondi, Kim K. Baldridge, Jay S. Siegel
DOI: 10.1039/B208871A
Ru-Catalyzed dehydrogenative synthesis of antimalarial arylidene oxindoles
Girish Singh Bisht, Akanksha M. Pandey, Moreshwar B. Chaudhari, Sandip G. Agalave, Abhishek Kanyal, Krishanpal Karmodiya, Boopathy Gnanaprakasam
DOI: 10.1039/C8OB01852A
Assignment of absolute configuration of a chiral phenyl-substituted dihydrofuroangelicin
Gennaro Pescitelli, Nina Berova, Tom L. Xiao, Roman V. Rozhkov, Richard C. Larock, Daniel W. Armstrong
DOI: 10.1039/B207652G
Rhodium-catalyzed cyclization of acceptor-substituted biphenyl α-diazoketones: a study of the substitution effect on chemoselectivity
Kuo-Hsin Chen, Yi-Jung Chiang, Jia-Liang Zhu
DOI: 10.1039/C8OB01489B
Purine-substituted imidazolium mesomeric betaines and their tautomeric N-heterocyclic carbenes. Formation of a cyclic borane adduct
Jiaxi Zhang, Eike G. Hübner, Jan C. Namyslo, Martin Nieger, Andreas Schmidt
DOI: 10.1039/C8OB01916A
Chemoselective synthesis of isolated and fused fluorenones and their photophysical and antiviral properties
Ismail Althagafi, Ranjay Shaw, Rahul Panwar, Shally, Chanda Sinha, Amit Kumar, Yong-Tang Zheng, Ramendra Pratap
DOI: 10.1039/C8OB01733F
Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control
Michal März, Michal Kohout, Tomáš Neveselý, Josef Chudoba, Dorota Prukała, Stanislaw Niziński, Marek Sikorski, Gotard Burdziński, Radek Cibulka
DOI: 10.1039/C8OB01822G
Eugenunilones A–H: rearranged sesquiterpenoids from Eugenia uniflora
Mu Chen, Jia-Qing Cao, Song Ang, Ting-Ni Zeng, Ni-Ping Li, Tang-Jia Yang, Jun-Shan Liu, Yan Wu, Wen-Cai Ye, Lei Wang
DOI: 10.1039/D1QO01629F
Vinyl sulfonyl chemistry-driven unidirectional transport of a macrocycle through a [2]rotaxane
Arthur H. G. David, Pablo García–Cerezo, Araceli G. Campaña, Francisco Santoyo–González, Victor Blanco
DOI: 10.1039/D1QO01491A
Reactions of 5-mercaptoazoles and pyridine-2-thiones with acetylenic esters. Selectivity of the formation of novel fused thiazin-4-ones and thiazolidin-4-ones
Vasiliy A. Bakulev, Vera S. Berseneva, Natalia P. Belskaia, Yury Yu. Morzherin, Andreiy Zaitsev, Wim Dehaen, Ingrid Luyten, Suzanne Toppet
DOI: 10.1039/B207854F
こちらもおすすめ
3-(2-オキサプロピル)ベンzoic酸はどのように合成されますか?
3-(2-オキサプロピル)ベンzoic酸は、ベンzoic酸とプロパノ酸をヒドロキシム化合物として反応させて生成します。具体的には、ベンzoic酸とプロパノ酸を反...
4-メチル-4-ピペリジニル-1-ピロリドイン甲酸の主な用途は何ですか?
4-メチル-4-ピペリジニル-1-ピロリドイン甲酸は、主に医薬品の合成材料や研究用物質として使用されます。さらに、一部の薬理学的研究にも応用されています。
Biotin-PEG3-oxyamine HCl塩について、適切な化合物名称に適用される法規ガイドラインは何ですか?
Biotin-PEG3-oxyamine HCl塩は、GHS( Globally Harmonized System of Classification and...
N-(4-イソチオシアネートフェニル)-2-メトキシアリニンはどのように合成されますか?
N-(4-イソチオシアネートフェニル)-2-メトキシアリニンは、4-イソチオシアノフェノールと2-メトキシアリニルアミンのアミニド反応を用いて合成されます。この...
金粉蕨亭2'-O-葡萄糖甙の主な用途は何ですか?
金粉蕨亭2'-O-葡萄糖甙は主に薬理研究や医薬品製造に使用され、抗炎症作用や抗がん作用などがあります。また、その構造や性質から、合成化学や化学生理学の研究にも用...
2-(2-ニトロフェニル)酢酸ヒドライドの物理化学的性質は何ですか?
2-(2-ニトロフェニル)酢酸ヒドライドのCAS番号は114953-81-0です。この化合物は白色結晶性粉末で、分子量は244.12です。水溶性は限られており、...
5-(ヒドロキシメチル)-2-チオキソ-2,3-ジヒドロピリミジン-4(1H)-オンを取り扱う際の実験室安全事項は何ですか?
この化合物は高活性のため、取り扱いには注意が必要です。PPE(個人保護具)としてゴーグル、ガントリー、および防滴シールドを着用することが推奨されます。ドラフトチ...
11-脱氢血栓烷 b2の市場動向や研究トレンドはどうですか?
11-脱氢血栓烷 b2は、血栓溶解・抗凝固作用に関する研究で注目を集めています。特に心血管疾患の治療法開発において、市場の需要が高まっています。研究トレンドとし...
3,3-二甲基哌啶-4-酮はどのように保存すればよいですか?
3,3-二甲基哌啶-4-酮は避光、常温、乾燥した場所で保存してください。容器は密閉し、遠くから火源を離して保管することを確認してください。
掲載誌
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.










![(2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure (2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure](https://static.chemtradehub.com/structs/173/173867-04-4-d2d3.webp)
![[4-Chloro-3-(diethylcarbamoyl)phenyl]boronic acid structure [4-Chloro-3-(diethylcarbamoyl)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/871/871332-68-2-0e3b.webp)


