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Preparation and characterisation of diamond-based stationary phases for high performance liquid chromatography

Peristyy, A (2015) Preparation and characterisation of diamond-based stationary phases for high performance liquid chromatography. PhD thesis, University of Tasmania.

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Abstract

The idea of using diamond and diamond containing materials in separation sciences has
attracted a strong interest in the past decade. The combination of a unique range of properties,
such as chemical inertness, mechanical, thermal and hydrolytic stability, excellent thermal
conductivity with minimal thermal expansion and intriguing adsorption properties makes
diamond a promising material for use in various modes of chromatography. This Thesis is
dedicated to the preparation and investigation of diamond based stationary phases for ultra
high-performance liquid chromatography. The Thesis consists of 6 chapters: introduction and
literature review, experimental Chapter, and four research Chapters.
The information about the recent research on the preparation of diamond based
stationary phases, their properties and chromatographic performance is summarised in
Chapter 1. Special attention is devoted to the dominant retention mechanisms evident for
particular diamond related materials, and their subsequent applicability to various modes of
liquid chromatography, including liquid chromatography carried out under the conditions of
high temperature and pressure. Advantages and drawbacks of diamond-based stationary
phases described in literature are analysed. According to the literature review, it is decided to
investigate chromatographic performance of non-modified non-porous high pressure high
temperature (HPHT) diamond with 1.6 μm particles and a surface area 5.1 m²·g⁻¹.
Chapter 2 contains the general information on materials and instrumentation used in
this work, as well as the description of methods and calculations.
A purification procedure for HPHT diamond is developed and its surface properties are
characterised using various physical chemical methods in Chapter 3. It is shown that this
material possesses a hydrophilic surface which displays various oxygen-containing groups,
including carboxyl, carbonyl, hydroxyl, and others. Next, optimisation of particle shape and
size distribution is performed by means of oxidative digestion and sedimentation. After that,
the column packing procedure is developed. It is shown that better column packings can be
achieved by using a water-based slurry with an addition of 10 mM NaOH, while use of
organic solvents does not provide stable packed beds. Finally, it is established that packing
pressure has to be kept as high as possible, and column after-packing conditioning with
HNO₃ helps to improve peak shape.
The resultant columns exhibit a maximum efficiency of 128,200 theoretical plates per
meter in normal phase (NP) liquid chromatography, as shown in Chapter 4. The retention
behaviour of several classes of compounds, including alkyl benzenes, polyaromatic
hydrocarbons, alkylphenylketones, phenols, and aromatic acids and bases are studied using nhexane
– IPA mixtures as a mobile phase. The results are compared with those observed for
microdispersed sintered detonation nanodiamond (MSDN) and porous graphitic carbon.
HPHT diamond revealed distinctive separation selectivity, which is orthogonal to that
observed for porous graphitic carbon (Hypercarb); while selectivities of HPHT diamond and
MSDN are similar. Owing to the non-porous nature of the particles, columns packed with
HPHT diamond exhibit excellent mass transfer, and separations of 4, 6 and 9 model
compounds are presented.
Furthermore, HPHT diamond is tested as a stationary phase in aqueous normal phase
(HILIC/ANP) chromatography using acetonitrile/water and methanol/water mobile phases in
Chapter 5. The retention of several classes of compounds is investigated, including
nucleobases, quaternary ammonium salts, carboxylic acids, phenols and their derivatives. The
column performance is studied within a large pH range (2.2-12.7) using several buffering
mixtures (trifluoroacetic, ammonium formate, ammonia and several hydroxides). The main
retention mechanisms for HPHT diamond include cation exchange and hydrogen bonding.
Both buffer and organic modifier (acetonitrile/methanol) have a crucial influence on the
HPHT diamond column selectivity. A complete selectivity reversal is observed for different
groups of solutes as a result of changes in mobile phase composition.
During the research on chromatographic properties of HPHT diamond, an assumption
is made that the adsorption of cations and anions on the surface of diamond has a strong
effect on its chromatographic performance. For example, it is shown that column
conditioning with HNO₃, H₂SO₄ or H₃PO₄ leads to different column selectivities in NPHPLC,
and the use of NaOH and KOH solutions of equal concentration in ANP-HPLC
results in different retention of nucleobases and phenolic compounds. Therefore, the
adsorption of cations and anions on the diamond surface is studied in Chapter 6. MSDN is
used for the investigation of the adsorption of inorganic cations and anions due to the higher
surface area of MSDN as compared to HPHT diamond.
The selectivity series Fe³⁺ > Al³⁺ > Cu²⁺ > Mn²⁺ > Zn²⁺ > Cd²⁺ > Co²⁺ > Ni²⁺ is found
for MSDN, and the adsorption capacity for these metals is between 2 and 5 μmol·g⁻¹. Counter
ions can contribute to the adsorption mechanism for transition metals, and the buffer
influence on the adsorption of metals is revealed. Accordingly, the adsorption of inorganic
anions (CH₃COO⁻, Cl⁻, B₄O₇²⁻, ClO₄⁻, I⁻, SO₄²⁻, C₂O₄²⁻, PO₄³⁻) on MSDN is investigated. The
adsorption capacity for inorganic anions is at levels of 50-150 μmol·g-1, depending on the
anion. For the first time, an anion exchange capacity is detected for detonation nanodiamond,
exceeding its cation-exchange capacity. Electrostatic interactions, formation of complexes
with hydroxyls and interactions with metal impurities contribute to the anion adsorption
mechanism, so anion adsorption selectivity over MSDN is different from common anion
exchangers. It is shown that the adsorption on MSDN obeys Langmuir law. The pH affects
the adsorption of SO₄²⁻, PO₄³⁻ and B₄O₇²⁻ differently due to different adsorption mechanisms.

Item Type: Thesis (PhD)
Keywords: Synthetic diamond, stationary phases, support characterisation, liquid chromatography, adsorption
Copyright Information:

Copyright 2015 the Author

Date Deposited: 21 Nov 2016 00:53
Last Modified: 21 Nov 2016 01:20
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