Xiaojun Lai

Hydrothermal synthesis of titanium dioxide nanoparticles studied employing in situ energy dispersive X-ray diffraction

Hydrothermal synthesis of titanium dioxide (TiO2) nanoparticles has been studied in situ using synchrotron radiation energy dispersive X-ray diffraction (EDXRD). The nanoparticles were produced from an acid (HNO3) and an alkaline (tetrabutylammonium hydroxide; TBA) peptized gel by hydrothermal treatment at 210 °C and 270 °C. The in situ EDXRD spectra clearly showed that pure TiO2 rutile phase nanoparticles were crystallized from HNO3 peptized gel, whereas pure anatase phase nanoparticles were produced from the TBA peptized gel. The EDXRD data shows that the rate of the particle formation increases with an increase in the process temperature for both processes. The powder X-ray diffraction (XRD) and selected area electron diffraction (SAED) data confirms the in situ EDXRD results. The TEM images show that the anatase nanoparticles have relatively homogeneous particle size and morphology distribution whereas the rutile nanoparticles exhibit bimodal size and morphology distribution attributed to Ostwald ripening effect during the hydrothermal treatment.

Investigation of the Effect of Hydroxypropyl Methylcellulose on the Phase Transformation and Release Profiles of Carbamazepine-Nicotinamide Cocrystal

ABSTRACTPurposeThe aim of this work was to investigate the influence of hydroxypropyl methylcellulose (HPMC) on the phase transformation and release profile of carbamazepine-nicotinamide (CBZ-NIC) cocrystal in solution and in sustained release matrix tablets.MethodsThe polymorphic transitions of the CBZ-NIC cocrystal and its crystalline properties were examined by differential scanning calorimetry (DSC), X-ray powder diffraction (XRPD), Raman spectroscopy, and scanning electron microscopy (SEM).ResultsThe apparent CBZ solubility and dissolution rate of CBZ-NIC cocrystal were constant in different concentrations of HPMC solutions. In a lower percentage of HPMC in the matrix tablets, the CBZ release profile of the CBZ-NIC cocrystal was nonlinear and declined over time. With an increased HPMC content in the tablets, the CBZ-NIC cocrystal formulation showed a significantly higher CBZ release rate in comparison with the other two formulations of CBZ III and the physical mixture.ConclusionsBecause of a significantly improved dissolution rate of the CBZ-NIC cocrystal, the rate of CBZ entering into solution is significantly faster than the rate of formation of the CBZ-HPMC soluble complex in solution, leading to a higher supersaturation level of CBZ and subsequently precipitation of CBZ dihydrate.

The influence of solution environment on the nucleation kinetics and crystallisability of para-aminobenzoic acid.

The influence of solvent type on the solution thermodynamics, nucleation-kinetics and crystal growth of alpha para-aminobenzoic acid (PABA) crystallising from supersaturated ethanol, acetonitrile and water solutions, is examined using poly-thermal analysis of the metastable zone width. Application of a recently proposed model for analysis of crystallisation kinetics (J. Cryst. Growth, 2010, 312, 698-704) indicates a solvent and concentration dependence of the nucleation mechanism and key nucleation parameters for the alpha form of PABA. The mechanism of nucleation is found to change from instantaneous to progressive with decreasing concentration and also when changing the solvent from ethanol to acetonitrile to water. The dependence of the nucleation mechanism is correlated to the kinetic component of the nucleation rate through calculated values of instantaneously nucleated crystallites, which increase from 1.40 × 109 m-3 in ethanol to 1.08 × 1010 m-3 in acetonitrile to 2.58 × 1010 m-3 in water. This in combination with low calculated number concentrations of interfacial tension between 1.13 and 2.71 mJ m-2, supports the conclusion that the kinetic component of the nucleation rate is more limiting when crystallising PABA from ethanol solutions in comparison to water solutions. This finding is further supported by molecular dynamics simulations of the solvation free energy of PABA, which is found to be greatest in water, -42.4 kJ mol-1 and lowest in ethanol, -58.5 kJ mol-1.

Habit modification of nearly perfect single crystals of potassium dihydrogen phosphate (KDP) by trivalent manganese ions studied using synchrotron radiation X-ray multiple diffraction in Renninger scanning mode

The X-ray multiple diffraction technique using synchrotron radiation is applied in the preliminary study of the habit modification of KDP samples as induced by incorporation of the trivalent transition metal cation Mn 3+ . High-resolution Renninger scans of pure and doped KDP were carried out using 400 as the primary reflection, echoing the fact that these impurity species were segregated in the {100} growth sector. The analysis of the Renninger scans of the doped KDP crystals is consistent with the presence of the impurity species chemically bound within the KDP crystal structure, as confirmed through the suppression of the huge observed peak asymmetry, characteristic of perfect crystals. In addition, an extra Renninger-scan peak measured for the doped material is indicative of the impurity atoms occupying interstitial crystallographic sites in the lattice, a result consistent with X-ray standing-wave measurements. Renninger-scan reflection curve widths and lattice parameter measurements reveal the decrease in crystalline perfection (increased mosaic spread, η) and lattice contraction of ca 0.4% in the a and c lattice directions at the surface plane for the Mn 3+ -doped KDP samples in comparison with the undoped crystals.

On-Line Analytical Techniques for Monitoring Crystallisation Processes of Organic Speciality Chemicals

Abstract In order to examine on-line batch crystallisation processes a new integrated batch process engineering laboratory has been established providing facilities for the on-line measurement and control of: • reactant supersaturation via ATR-FTIR spectroscopy; • crystal size via acoustic attenuation spectroscopy; • particle perfection and polymorphic form via X-ray diffraction; • crystallisation on-set and meta-stable zone width via UV vis spectroscopic turbidometric measurements. These facilities are complemented via assessment of reactant mixing as measured via laser doppler anemometry and simulated using multi-phase computational fluid dynamics. An overview of the planned research programme and material systems to be examined are presented:

Role of polymers in solution and tablet-based carbamazepine cocrystal formulations

The aim of this study was to evaluate the influence of three chemically diverse polymers, namely hydroxypropylmethylcellulose acetate succinate (HPMCAS), polyvinylpyrrolidone (PVP) and polyethylene glycol (PEG) on the phase transformation of three carbamazepine (CBZ) cocrystals including carbamazepine–nicotinamide (CBZ–NIC), carbamazepine–saccharin (CBZ–SAC) and carbamazepine–cinnamic acid (CBZ–CIN) in solution and tablet-based formulations. Based on the solubility and powder dissolution studies, it is demonstrated that cocrystals can be easily formulated through a simple solution formulation or powder formulation to generate supersaturated concentrations and faster dissolution rates to overcome those drugs with solubility and/or dissolution limited bioavailability. However, a polymer-based CBZ cocrystal tablet formulation has not shown any advantage of an improved CBZ release rate compared with the formulation of CBZ III or physical mixtures of CBZ III and coformers. This is in contrast to the solution behaviours of CBZ cocrystals in the solubility and powder dissolution tests because crystallization of the stable solid form of CBZ dihydrate (CBZ DH) within the tablet has taken place, leading to a reduced drug release rate and incomplete release. The mechanism of a polymer inhibition effect on drug precipitation in solution has been elucidated through investigating the molecular interactions among CBZ, coformers and polymers in solution using infrared spectroscopy. Finally, a formulation strategy has been proposed to capture the significant advantages of cocrystals.

Data for crystallisation, dissolution and saturation temperatures of the ternary system: Hexadecane and octadecane representative in fuel solvents

The data presented in this article relates to the crystallisation of hexadecane (C16H34) and octadecane (C18H38), being the predominant alkanes present in hydrotreated vegetable oil (HVO), from solvents representative of fuel (dodecane, toluene and kerosene). Data was collected for eleven C16H34/C18H38 compositions for each solvent used. Raw crystallisation and dissolution data is provided over a range of solution concentrations and cooling rates used under a poly-thermal crystallisation methodology. Equilibrium saturation temperature data is also presented for each composition, concentration and solvent system, indicating the trend in solubility for each solution.

The thermal expansion coefficients of the alpha and beta polymorphic forms of p-aminobenzoic acid in relation to their bulk crystal chemistry

The thermal expansion behaviour of the alpha and beta polymorphs of para-aminobenzoic acid are presented and discussed in terms of the bulk crystal chemistry and the associated strengths of the constituent intermolecular synthons for these two materials. Analysis of temperature dependant powder diffraction data over the temperature range 298.15–403.15 K facilitates calculation of the linear thermal expansion coefficients: αa = 8.36 × 10−06 K−1, αb = 94.5 × 10−06 K−1 and αc = 9.91 × 10−06 K−1 for the alpha polymorph and αa = 21.5 × 10−06 K−1, αb = 48.5 × 10−06 K−1 and αc = 2.22 × 10−06 K−1 for the beta polymorph. The exceptionally large increase in the thermal expansion of the b axis for the alpha form reflects the weak dispersive interactions which propagate along this axis. In contrast, the a and c axes contain relatively strong hydrogen bonds which stabilise the lattice and limit thermal expansion. The thermal expansion of the beta form reflects the more isotropic nature of the intermolecular synthons for this polymorph in comparison to the alpha form. The thermal expansion of the b axis of the beta form is larger than that of the a and c axes but to a much lesser extent than that observed for the alpha form. This is rationalised through identification of a hydrogen bonding component which contributes to the stabilisation of the b axis in comparison to the almost fully dispersive nature found in the alpha structure.

An instrument for combining x-ray multiple diffraction and x-ray topographic imaging for examining crystal microcrystallography and perfection.

Diffraction imaging using x-ray topography (XRT) and x-ray multiple diffraction (XRMD) provide valuable tools for examining the growth defects in crystals and the distributions from ideal lattice symmetry (microcrystallography). The topographic x-ray multiple diffraction microprobe (TMDM) combines the complementary aspects of both techniques enabling XRT and XRMD studies within the same instrument providing a useful resource for the structural characterization of materials that are not very stable in vacuum and electron beam environments. The design of the TMDM instrument is described together with data taken on GaAs (001) and potassium dihydrogen phosphate (001).

The Information Content In Nir Spectral Data For Slurries Of Organic Crystals

Despite being widely used in agriculture, food production and environmental monitoring and regarded as on‐line chromatograph in petrochemical and biochemical industries, near infrared spectroscopy (NIR) has found difficulties in its application to processes of particle formation through crystallization or precipitation where solids suspended in solutions cause problems in instrumentation as well as distortion of the spectra. The research work reported here was motivated by the speculative idea that the effect of particles on the NIR spectra in effect brings an opportunity instead: the spectra might contain useful information of both the solid and liquid phases. Through carefully designed experiments using both glutamic acid solutions and slurries of varied solid concentrations and particle size and temperature ranges and with the help of chemometric data analysis, it was found that the NIR spectra clearly contain sensitive information about the size, solid concentration, liquid concentration as well as po...