ATR-FTIR spectroscopy as a tool to probe surface adsorption on nanoparticles at the liquid–solid interface in environmentally and biologically relevant media

Literature Information

Publication Date 2013-12-02
DOI 10.1039/C3AN01684F
Impact Factor 4.616
Authors

Imali A. Mudunkotuwa, Alaa Al Minshid, Vicki H. Grassian


View Original

Abstract

Given the importance of nanoparticle surface composition in nanotoxicology, analytical tools that can probe nanoparticle surfaces in aqueous media are crucial but remain limited. Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy is a technique capable of in situ characterization of the liquid–solid interface to probe surface adsorption on nanoparticle surfaces in environmentally and biologically relevant media. Furthermore, given that the interfacial region in these media is dynamic, ATR-FTIR spectroscopy facilitates monitoring these dynamics by interrogating a layer of immobilized nanoparticles coated on the ATR element while changing the overlying aqueous phase. The molecular information acquired from this technique allows for the determination of the adsorption mode, including conformational and structural changes of the coordinating ligand, and can directly measure ligand displacement reactions. Furthermore, in some cases, ATR-FTIR spectroscopy can be used as a quantitative surface analytical tool. In this article, we briefly review the fundamentals of the technique and then provide several examples of using ATR-FTIR spectroscopy to probe nanoparticle surfaces in general with respect to: (i) the adsorption of different environmentally and biologically relevant coordinating ligands; (ii) competitive ligand adsorption and; (iii) the determination of kinetic and thermodynamic parameters. We have also investigated surface adsorption of TiO2 nanoparticles in different biological media typically used for toxicity studies and show that the surface composition of TiO2 nanoparticles depends to a large extent on the composition of the medium due to surface adsorption. This result has important implications for the interpretation of toxicity data as well as inter-comparisons between toxicity studies.

Related Literature

Noncovalent attachment of oxidenanoparticles onto carbon nanotubes using water-in-oil microemulsions

Jing Sun, Lian Gao, Mikio Iwasa

2004-02-27 Communication

DOI: 10.1039/B400817K

Porphyrin ring contraction: a one-pot reaction leading to divalent corroles

Christophe Jeandon, Romain Ruppert, Henry J. Callot

2004-04-02 Communication

DOI: 10.1039/B400812J

Phase transitions in calcium nitrate thin films

Hind A. Al-Abadleh, B. J. Krueger, J. L. Ross, V. H. Grassian

2003-10-14 Communication

DOI: 10.1039/B308632A

First in-situSAXS studies of the mesostructuration of spherical silica and titania particles during spray-drying process

C. Boissiere, D. Grosso, H. Amenitsch, A. Gibaud, A. Coupé, N. Baccile, C. Sanchez

2003-10-14 Communication

DOI: 10.1039/B308694A

“Green”-enzymatic synthesis of pegylated phenolic macromer and polymer

Ferdinando Bruno, Virinder S. Parmar, Jayant Kumar, Arthur C. Watterson, Kethinni G. Chittibabu, Lynne A. Samuelson

2004-03-02 Communication

DOI: 10.1039/B400404C

Long-term pervaporation performance of microporous methylated silica membranes

Jean Campaniello, Charles W. R. Engelen, Wim G. Haije, Paul P. A. C. Pex, Jaap F. Vente

2004-02-27 Communication

DOI: 10.1039/B401496K

Novel label-free DNA sensors based on poly(3,4-ethylenedioxythiophene)

K. Krishnamoorthy, Rajesh S. Gokhale, Aliasgar Q. Contractor, Anil Kumar

2004-02-24 Communication

DOI: 10.1039/B316794A

Mesoporous iron phosphate as an active, selective and recyclable catalyst for the synthesis of nopol by Prins condensation

Unnikrishnan R. Pillai, Endalkachew Sahle-Demessie

2004-02-23 Communication

DOI: 10.1039/B313747C

Unusual reactions of N-allylic difluoroenamines under thermal conditions

Hideki Amii, Yutaka Ichihara, Takashi Nakagawa, Takeshi Kobayashi, Kenji Uneyama

2003-10-20 Communication

DOI: 10.1039/B309696C

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Analyst

Analyst
CiteScore: 7.8
Self-citation Rate: 5.6%
Articles per Year: 653

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.