Swelling of ionic microgel particles in the presence of excluded-volume interactions: a density functional approach
文献信息
Arturo Moncho-Jordá
In this work a new density functional theory framework is developed to predict the salt-concentration dependent swelling state of charged microgels and the local concentration of monovalent ions inside and outside the microgel. For this purpose, elastic, solvent-induced and electrostatic contributions to the microgel free energy are considered together with the free energy of the ions. In addition to the electrostatic interaction, the model explicitly considers both the microgel–ion excluded-volume (steric) repulsion and the ionic correlations, in such a way that the formalism is consistent with the Hypernetted-Chain Closure approximation (HNC). We explore the role that the solvent quality, chain elasticity, salt concentration and microgel bare charge play on the swelling state, the effective charge and on the ionic density profiles. Our results show that the microgel–ion steric exclusion foments the increase of the particle size up to 10%. The role that the steric effect plays on the counterion distribution becomes more important when the microgel approaches the shrunken configuration, developing an accumulation peak at the microgel interface and a reduction in the inner core of the microgel that induce a significant increase of the microgel effective charge. We further find that deep inside the particle charge electroneutrality is achieved and a Donnan potential corrected by the steric exclusion is established.
期刊推荐

Physical Chemistry Chemical Physics

Photochemical & Photobiological Sciences

Journal of Enzyme inhibition and Medicinal Chemistry

Angewandte Chemie International Edition

Green Chemistry

European Journal of Organic Chemistry

Faraday Discussions

Current Pharmaceutical Biotechnology

Nature Reviews Drug Discovery

Foundations of Chemistry
相关文献
Development of a robust reagent for the two-carbon homologation of aldehydes to (E)-α,β-unsaturated aldehydes in water
James McNulty, Carlos Zepeda-Velázquez, David McLeod
DOI: 10.1039/C3GC41383G
Production of biomass-derived furanic ethers and levulinate esters using heterogeneous acid catalysts
Patrícia Neves, Margarida M. Antunes, Patrícia A. Russo, Joana P. Abrantes, Sérgio Lima, Auguste Fernandes, Martyn Pillinger, Sílvia M. Rocha, Maria F. Ribeiro, Anabela A. Valente
DOI: 10.1039/C3GC41908H
Structural features of ionic liquids: consequences for material preparation and organic reactivity
Anthony F. Masters, Thomas Maschmeyer
DOI: 10.1039/C3GC41313F
Synthesis of acetylenic alcohols with calcium carbide as the acetylene source
Yin Ngai Sum, Dingyi Yu, Yugen Zhang
DOI: 10.1039/C3GC41269E
A new generation of aprotic yet Brønsted acidic imidazolium salts: effect of ester/amide groups in the C-2, C-4 and C-5 on antimicrobial toxicity and biodegradation
Rohitkumar G. Gore, Lauren Myles, Marcel Spulak, Ian Beadham, Teresa M. Garcia, Stephen J. Connon, Nicholas Gathergood
DOI: 10.1039/C3GC40992A
AIBN-initiated metal free amidation of aldehydes using N-chloroamines
Rajeshwer Vanjari, Tirumaleswararao Guntreddi, Krishna Nand Singh
DOI: 10.1039/C3GC41548A
Asymmetric anti-Mannich reactions in continuous flow
Rafael Martín-Rapún, Sonia Sayalero
DOI: 10.1039/C3GC41444B
Productive sugar isomerization with highly active Sn in dealuminated β zeolites
Jan Dijkmans, Dries Gabriëls, Michiel Dusselier, Filip de Clippel, Pieter Vanelderen, Kristof Houthoofd, Annelies Malfliet, Yiannis Pontikes, Bert F. Sels
DOI: 10.1039/C3GC41239C
A simple and highly effective water-compatible organocatalytic system for asymmetric direct Michael reactions of linear aldehydes to maleimides
Yupu Qiao, Allan D. Headley
DOI: 10.1039/C3GC41024B
Solid supported platinum(0) nanoparticles catalyzed chemo-selective reduction of nitroarenes to N-arylhydroxylamines
DOI: 10.1039/C3GC41179F
您可能还喜欢
3 - (二氟甲基)-1 -氟苯(CAS号:26029-52-7)适用哪些法规指南?
3 - (二氟甲基)-1 -氟苯需遵循联合国全球化学品统一分类和标签制度(GHS),包括急性毒性、皮肤腐蚀/刺激、严重眼损伤/眼刺激等分类。同时,该化合物还需符...
3,5-二甲基苯胺(CAS号:108-69-0)通常如何合成?
3,5-二甲基苯胺通常通过乙苯的氨解反应合成。反应中使用硫酸作为催化剂,反应温度为120-130°C。乙苯在硫酸存在下与氨反应,生成3,5-二甲基苯胺和苯胺副产...
3-甲基异噻唑-5-胺(CAS号:24340-76-9)安全吗?
3-甲基异噻唑-5-胺在适当使用和储存条件下是相对安全的,但在操作时应注意防护措施。应避免吸入粉尘,避免与皮肤和眼睛直接接触。在操作过程中,应穿戴适当的防护装备...
3-(1,3-Thiazol-2-yl)-1H-indole(CAS号:135531-86-1)通常如何合成?
3-(1,3-噻唑-2-基)-1H-吲哚通常通过多步合成方法制备。首先,由噻唑-2-基溴化物和吲哚进行偶联反应,得到中间体。然后,通过还原反应将中间体转化为所需...
4-溴-2-氟苯甲基氯(CAS号:85510-82-3)的主要用途是什么?
4-溴-2-氟苯甲基氯主要用于有机合成中间体,特别是在医药、农药和染料等领域。作为一种具有特定结构的化合物,它在合成复杂有机分子时扮演重要角色。
处理Fmoc-β-(3-噻吩基)-D-Ala-OH(CAS号:220497-90-5)时应注意哪些实验室安全事项?
处理Fmoc-β-(3-噻吩基)-D-Ala-OH时,应佩戴防护手套、护目镜和实验服。操作应在通风橱内进行。如发生泄露,应立即用大量水冲洗,并通知实验室管理人员...
氮化硅(CAS号:12033-89-5)通常如何合成?
氮化硅通常通过氮化硅的直接反应合成,即在高温下将四氯化硅与氨气反应。具体步骤是将四氯化硅和氨气混合并加热至1300-1700℃,在该条件下,四氯化硅与氨气反应生...
Cetirizine EP Impurity B DiHCl(CAS号:1000690-91-4)通常如何合成?
Cetirizine EP Impurity B DiHCl通常通过一锅法合成,首先将4-氯苯基-苯甲基氯甲酸酯与1-哌嗪乙酸反应,生成相应的酸,然后与盐酸反应...
如何储存1-哌啶-4-基丁-1-酮(CAS号:3509-15-7)?
1-哌啶-4-基丁-1-酮应储存在阴凉、干燥的地方,避免阳光直射。存储容器应密封,并确保通风良好。建议储存温度不超过25℃,湿度保持在相对较低的水平。
如何处理含有VORUCICLIB(CAS号:1000023-04-0)的废料?
含有VORUCICLIB的废料应进行专业的收集和处理,包括使用适当的容器进行隔离,避免与其他化学品接触。处理方法通常包括化学中和、沉淀反应或吸附过程,随后进行焚...
来源期刊
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.
![5-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amine structure 5-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amine structure](https://cnstatic.chemtradehub.com/structs/122/1227210-33-4-8d64.webp)



![Pyrazolo[1,5-a]pyridine-3-carbothioamide structure Pyrazolo[1,5-a]pyridine-3-carbothioamide structure](https://cnstatic.chemtradehub.com/structs/885/885275-44-5-aae0.webp)