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Quantifying surface groups on aminated silica nanoparticles of different size, surface chemistry, and porosity with solution NMR, XPS, optical assays, and potentiometric titration.

作者信息

Tavernaro Isabella, Rajotte Isabelle, Thibeault Marie-Pier, Sander Philipp C, Kodra Oltion, Lopinski Gregory, Radnik Jörg, Johnston Linda J, Brinkmann Andreas, Resch-Genger Ute

机构信息

Division Biophotonics, Federal Institute for Materials Research and Testing (BAM) Richard-Willstätter-Str. 11 12489 Berlin Germany

Metrology Research Centre, National Research Council Canada Ottawa Ontario K1A 0R6 Canada

出版信息

Nanoscale Adv. 2025 Sep 10. doi: 10.1039/d5na00794a.

Abstract

We assessed the quantification of surface amino functional groups (FGs) for a large set of commercial and custom-made aminated silica nanoparticles (SiO NPs) with sizes of 20-100 nm, prepared with different sol-gel routes, different amounts of surface amino FGs, and different porosity with four methods providing different, yet connected measurands in a bilateral study of two laboratories, BAM and NRC, with the overall aim to develop standardizable measurements for surface FG quantification. Special emphasis was dedicated to traceable quantitative magnetic resonance spectroscopy (qNMR) performed with dissolved SiO NPs. For the cost efficient and automatable screening of the amount of surface amino FGs done in a first step of this study, the optical fluorescamine assay and a potentiometric titration method were utilized by one partner, , BAM, yielding the amount of primary amino FGs accessible for the reaction with a dye precursor and the total amount of (de)protonatable FGs. These measurements, which give estimates of the minimum and maximum number of surface amino FGs, laid the basis for quantifying the amount of amino silane molecules with chemo-selective qNMR with stepwise fine-tuned workflows, involving centrifugation, drying, weighting, dissolution, measurement, and data evaluation steps jointly performed by BAM and NRC. Data comparability and relative standard deviations (RSDs) obtained by both labs were used as quality measures for method optimization and as prerequisites to identify method-inherent limitations to be later considered for standardized measurement protocols. Additionally, the nitrogen (N) to silicon (Si) ratio in the near-surface region of the SiO NPs was determined by both labs using X-ray photoelectron spectroscopy (XPS), a well established surface sensitive analytical method increasingly utilized for microparticles and nano-objects which is currently also in the focus of international standardization activities. Overall, our results underline the importance of multi-method characterization studies for quantifying FGs on NMs involving at least two expert laboratories for effectively identifying sources of uncertainty, validating analytical methods, and deriving NM structure-property relationships.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ff/12539595/16f37cb47d82/d5na00794a-f1.jpg

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