Particle size analysis and characterization of nanodiamond dispersions in water and dimethylformamide by various scattering and diffraction methods.

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985858%3A_____%2F20%3A00520526" target="_blank" >RIV/67985858:_____/20:00520526 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/49777513:23640/20:43958494

Výsledek na webu

<a href="http://hdl.handle.net/11104/0307075" target="_blank" >http://hdl.handle.net/11104/0307075</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/s11051-020-4755-3" target="_blank" >10.1007/s11051-020-4755-3</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Particle size analysis and characterization of nanodiamond dispersions in water and dimethylformamide by various scattering and diffraction methods.

Popis výsledku v původním jazyce

Over the past few decades, detonation nanodiamonds (NDs) have gained increased attention due to their unique physicochemical properties. Various methods for preparation of ND suspensions have been introduced. This paper presents thermally annealed nanodiamonds dispersed via sonication and separated by centrifugation in deionized water and dimethylformamide in five weight concentrations ranging from 0.05 to 1 wt%. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were applied to study the thermal behavior of NDs. Crystallographic properties of air-annealed and dispersed NDs were examined by means of X-ray diffraction (XRD). Nanodiamond dispersions were analyzed by static light scattering (SLS), dynamic light scattering (DLS), ultra-small- and small-angle X-ray scattering (USAXS/SAXS), and high-resolution transmission electron microscopy (HRTEM). SLS and DLS give similar results of ND− aggregates mean size between ~ 61 and 73 nm, regardless of solvent type and nanoparticle concentration. For dispersions with increasing concentrations of NDs, neither increased aggregate size nor different kinetics of separation during sonication and centrifugation were observed. USAXS/SAXS provided the aggregates size (2Rg) in the range from 57 to 65 nm and size of primary particles from 5.4 to 5.8 nm. HRTEM also showed presence of larger aggregates with tens of nanometers in size in both water and DMF dispersions, and size of primary particles ranging from 5.5 to 6 nm in very good agreement with SAXS.n

Název v anglickém jazyce

Particle size analysis and characterization of nanodiamond dispersions in water and dimethylformamide by various scattering and diffraction methods.

Popis výsledku anglicky

Over the past few decades, detonation nanodiamonds (NDs) have gained increased attention due to their unique physicochemical properties. Various methods for preparation of ND suspensions have been introduced. This paper presents thermally annealed nanodiamonds dispersed via sonication and separated by centrifugation in deionized water and dimethylformamide in five weight concentrations ranging from 0.05 to 1 wt%. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were applied to study the thermal behavior of NDs. Crystallographic properties of air-annealed and dispersed NDs were examined by means of X-ray diffraction (XRD). Nanodiamond dispersions were analyzed by static light scattering (SLS), dynamic light scattering (DLS), ultra-small- and small-angle X-ray scattering (USAXS/SAXS), and high-resolution transmission electron microscopy (HRTEM). SLS and DLS give similar results of ND− aggregates mean size between ~ 61 and 73 nm, regardless of solvent type and nanoparticle concentration. For dispersions with increasing concentrations of NDs, neither increased aggregate size nor different kinetics of separation during sonication and centrifugation were observed. USAXS/SAXS provided the aggregates size (2Rg) in the range from 57 to 65 nm and size of primary particles from 5.4 to 5.8 nm. HRTEM also showed presence of larger aggregates with tens of nanometers in size in both water and DMF dispersions, and size of primary particles ranging from 5.5 to 6 nm in very good agreement with SAXS.n

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2020

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Nanoparticle Research

ISSN

1388-0764

e-ISSN

—

Svazek periodika

22

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

17

Strana od-do

34

Kód UT WoS článku

000511890900001

EID výsledku v databázi Scopus

2-s2.0-85077868422