ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025
Predictable Self-Assembly as an Unexplored Key Factor Influencing Membrane Separation: Insights from Monophenols.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Predictable Self-Assembly as an Unexplored Key Factor Influencing Membrane Separation: Insights from Monophenols.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
While nanofiltration (NF) holds promise for separating small molecules, effectively separating structurally similar compounds like monophenols remains challenging. This study unveils a novel NF separation strategy based on the often-overlooked phenomenon of solute self-assembly. Using a combination of experimental and computational approaches, a direct link between monophenol self-assembly and rejection behavior during NF is established. The self-assembly of monophenols, primarily driven by π-π stacking interactions, is shown to significantly influence their rejection rates, with larger, more numerous self-assemblies experiencing higher rejection. Furthermore, a clear relationship between monophenol structures and self-assembly strength is established, revealing that the number and Hydrogen (H)-bonding capacity of substituents on the aromatic ring dictate the propensity for self-assembly. This insight enables the development of a predictive model for monophenol self-assembly, which is validated through NF experiments using binary mixtures, confirming that predictable differences in self-assembly behavior can be leveraged for selective separation. This study establishes solute self-assembly as a tunable parameter for enhancing NF separation of similarly sized molecules.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.