ArticleLangmuir : the ACS journal of surfaces and colloids2014
Enantiomeric selective adsorption of amino acid by polysaccharide composite materials.
Article in Langmuir : the ACS journal of surfaces and colloids, 2014. 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, 17 citations in OpenAlex.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
A composite containing cellulose (CEL) and chitosan (CS) synthesized by a simple and recyclable method by using butylmethylimmidazolium chloride, an ionic liquid, was found to exhibit remarkable enantiomeric selectivity toward the adsorption of amino acids. The highest adsorption capacity and enantiomeric selectivity are exhibited by 100% CS. A racemic amino acid can be enantiomerically resolved by 100% CS in about 96-120 h. Interestingly, adsorption by 50:50 CEL/CS is more similar to that by 100% CS than to 100% CEL. Specifically, whereas 100% CEL has the lowest adsorption capacity and enantiomeric selectivity, 50:50 CEL/CS has sufficient enantiomeric selectivity to enable it to be used for chiral resolution. This is significant because in spite of its high enantiomeric selectivity 100% CS cannot practically be used because it has relatively poor mechanical properties and undergoes extensive swelling. Adding 50% CEL to CS substantially improves the mechanical properties and reduces its swelling while it retains sufficient enantiomeric selectivity to enable it to be used for routine chiral separations. The kinetic results indicate that the enantiomerically selective adsorption is due not to the initial surface adsorption but rather to the subsequent stage in which the adsorbate molecules diffuse into the pores within the particles of the composites and consequently are adsorbed by the interior of each particle. The strong intermolecular and intramolecular hydrogen bond network in CEL enables it to adopt a very dense structure that makes it difficult for adsorbate molecules to diffuse into its interior, thereby leading to low enantiomeric selectivity. Compared to hydroxy groups, amino groups cannot form strong hydrogen bonds. The hydrogen bond network in CS is not as extensive as in CEL, and its inner structure is relatively less dense than that of CEL. Adsorbate molecules can, therefore, diffuse from the outer surface to its inner structure relatively more easily than in CEL, thereby leading to higher enantiomeric selectivity for 100% CS.
Indexed as
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.