Characterization of nanoparticles of lidocaine in w/o micro emulsions using small-angle neutron scattering and dynamic light scattering

Microemulsions (MEs) are of special interest because a variety of reactants can be introduced into the nanometer-sized aqueous domains, leading to materials with controlled size and shape [1,2]. In the past few years, significant research has been conducted in the reverse ME-mediated synthesis of organic nanoparticles [3,4]. In this study, a w/o ME medium was employed for the synthesis of lidocaine by direct precipitation in w/o microemulsion systems: water/isopropylpalmitat/Tween80/Span80. The particle size as well as the location of nanoparticles in the ME droplet were characterized by means of dynamic light scattering (DLS) and small angle neutron scattering (SANS). It is observed that lidocaine precipitated in the aqueous cores because of its insolubility in water. Hydrodynamic radius and gyration radius of microemulsion droplets were estimated as ∼15 nm and ∼4.50 nm from DLS and SANS respectively. Furthermore, different size parameters obtained by DLS and SANS experiments were compared     

Detection of submicron-sized raft-like domains in membranes by small-angle neutron scattering

Using coarse grained models of heterogeneous vesicles we demonstrate the potential for small-angle neutron scattering (SANS) to detect and distinguish between two different categories of lateral segregation: 1) unilamellar vesicles (ULV) containing a single domain and 2) the formation of several small domains or “clusters” (~10 nm in radius) on a ULV. Exploiting the unique sensitivity of neutron scattering to differences between hydrogen and deuterium, we show that the liquid ordered (lo) DPPC-rich phase can be selectively labeled using chain deuterated dipalymitoyl phosphatidylcholine (dDPPC), which greatly facilitates the use of SANS to detect membrane domains. SANS experiments are then performed in order to detect and characterize, on nanometer length scales, lateral heterogeneities, or so-called “rafts”, in ~30 nm radius low polydispersity ULV made up of ternary mixtures of phospholipids and cholesterol. For 1:1:1 DOPC:DPPC:cholesterol (DDC) ULV we find evidence for the formation of lateral heterogeneities on cooling below 30 °C. These heterogeneities do not appear when DOPC is replaced by SOPC. Fits to the experimental data using coarse grained models show that, at room temperature, DDC ULV each exhibit approximately 30 domains with average radii of ~10 nm.     

Small angle neutron scattering and small angle X-ray scattering studies of platinum-loaded carbon foams

The morphology of carbon nanofoam samples comprising platinum nanoparticles dispersed in the matrix was characterized by small angle neutron scattering (SANS) and small angle X-ray scattering (SAXS) techniques. Results show that the structure of pores of carbon matrix exhibits a mass (pore) fractal nature and the average radius of the platinum particles is about 2.5 nm. The fractal dimension as well as the size distribution parameters of platinum particles varies markedly with the platinum content and annealing temperature. Transmission electron micrographs of the samples corroborate the SANS and SAXS results.      

Quantitative analysis of fine nano-sized precipitates in low-carbon steels by small angle neutron scattering

The small angle neutron scattering (SANS) technique was used to determine the nano-sized precipitates in interstitial free (IF) and low-carbon (LC) steels with a hot-rolling temperature. The real-space direct model fitting method was applied to quantitatively analyze the SANS data. The magnetic and chemical properties of precipitates in the samples were also investigated by separation and comparison of nuclear and magnetic SANS scattering data. The size distribution of precipitates in the IF steel is in good agreement with the microstructure observation using transmission electron microscopy. The results revealed that the IF steel had two types of non-magnetic precipitates, Ti₄C₂S₂ and TiC, with the average size of about 30 nm in diameter and little difference in chemical composition. In case of commercial LC steel, the fine and large precipitates are identified as MnS and Fe₃C, respectively. The average size of spherical MnS precipitates was about 4.8 nm in radius and the distribution is isotropic. It is likely that the LC steels have almost the same composition and a similar size as precipitates such as MnS and Fe₃C with different finishing delivery temperatures. Interestingly, the average size and volume fraction of fine precipitates showed no significantly changes under the different finishing delivery temperatures.     

Structural investigation on gamma-irradiated polyacrylamide hydrogels using small-angle neutron scattering and ultraviolet–visible spectroscopy

Small-angle neutron scattering (SANS) and ultraviolet (UV)–visible spectroscopic techniques are used to investigate the microstructural changes in polyacrylamide (PAAm) hydrogels on gamma irradiation. SANS measurements have revealed the presence of inhomogeneities in nanometre scale and reduction of their size with increase in dose. Analysis of SANS data also revealed the increase in the correlation length with increase in dose. The extinction coefficient obtained from the UV–visible spectroscopic studies exhibited λ^?β dependence between 500 and 700 nm and is understood to arise from the existence of scatterers (inhomogeneities) in submicron scale in PAAm hydrogels. The increase in value of exponent β with increase in dose indicates that the size of scatterers decrease with increase in dose.     

Small-angle neutron and dynamic light scattering study of gelatin coacervates

The state of intermolecular aggregates and that of folded gelatin molecules could be characterized by dynamic laser light and small-angle neutron scattering experiments, which implied spontaneous segregation of particle sizes preceding coacervation, which is a liquid-liquid phase transition phenomenon. Dynamic light scattering (DLS) data analysis revealed two particle sizes until precipitation was reached. The smaller particles having a diameter of ～50 nm (stable nanoparticles prepared by coacervation method) were detected in the supernatant, whereas the inter-molecular aggregates having a diameter of ～400 nm gave rise to coacervation. Small-angle neutron scattering (SANS) experiments revealed that typical mesh size of the networks exist in polymer dense phase (coacervates) [1]. Analysis of the SANS structure factor showed the presence of two length scales associated with this system that were identified as the correlation length or mesh size, ξ = 10.6 Å of the network and the other is the size of inhomogeneities = 21.4 Å. Observations were discussed based on the results obtained from SANS experiments performed in 5% (w/v) gelatin solution at 60°C (ξ = 50 Å, ζ = 113 Å) and 5% (w/v) gel at 28°C (ξ = 47 Å, ζ = 115 Å) in aqueous phase [2] indicating smaller length scales in coacervate as compared to sol and gel.     

Formation of fullerene clusters in carbon disulfide: Data on small-angle neutron scattering and molecular dynamics

Fullerene solutions in carbon disulfide are studied by small-angle neutron scattering (SANS). In addition to earlier experiments on the given system, the range of measured transmitted impulses is extended and the influence of solution preparation methods on C₆₀ cluster formation in these solutions is studied. It is shown that the formation of large C₆₀ clusters (with a size of about 10 nm) is due to nonequilibrium methods of solution preparation. For nonequilibrium dissolution, there is a 10% excess of the observed fullerene size in the solution over the calculated value. It has been established by simulation of the C₆₀/CS₂ interface by molecular dymanics methods that inclusion of how solvent molecules are organized on the C₆₀ surface leads to a decrease in the fullerene size in the solution, observed by using SANS. In this paper, the effect of excess R _g is explained by the presence of small clusters in the solution (approximately 10% of dissolved C₆₀ molecules). It is discovered that there is a time variation in the concentration of the saturated solution. The explanation of this effect using a model of formation and sedimentation of large clusters (with a size of 100 nm or more) is proposed.     

De-mixing dynamics of a binary liquid system in a controlled-pore glass. A neutron spin-echo spectroscopy and small angle neutron scattering study

The temperature-induced microphase separation of the binary liquid system iso-butyric acid+heavy water (iBA + D(2)O) in a mesoporous silica glass (CPG-10-75) of nominal pore width 7.5 nm was investigated by neutron spin-echo spectroscopy (NSE) and neutron small-angle scattering (SANS). Two mixtures of different composition were studied at different scattering angles at temperatures above and below the bulk phase transition temperature. The phase separation in the pore space is found to occur at a lower temperature than the bulk transition and extends over a significant temperature range. The effective diffusion coefficient derived from NSE at low scattering angles is found to decrease by one order of magnitude from 70 degrees C to 20 degrees C. This observation is attributed to the growing size of concentration fluctuations having a cut-off at ca. 8 nm, which corresponds to the mean pore size. The dynamics of the concentration fluctuations appears to be strongly influenced by the confinement in the pores, as it differs strongly from the bulk behaviour. These results are consistent with the preliminary results of the SANS study.     

Small angle neutron scattering at very high time resolution: Principle and simulations of ‘TISANE’

The time resolution of SANS experiments is generally limited by frame overlap to some ms. We report on a new time-resolved stroboscopic SANS method, called TISANE, offering μs time resolution without a major sacrifice in intensity by making use of very large frame overlap. We may explore a new field in neutron scattering and complement the emerging field of time resolved small angle X-ray scattering. Here we discuss the principle of TISANE, its mathematical treatment and its limitations.     

Nano-meter-sized domain formation in lipid membranes observed by small angle neutron scattering

Using a contrast matching technique of small angle neutron scattering (SANS), we have investigated a phase separation to liquid-disordered and liquid-ordered phases on ternary small unilamellar vesicles (SUVs) composed of deuterated-saturated, hydrogenated-unsaturated phosphatidylcholine lipids and cholesterol, where the equilibrium size of these domains is constrained to less than 10nm by the system size. Below a miscibility temperature, we observed characteristic scattering profiles with a maximum, indicating the formation of nano-meter-sized domains on the SUVs. The observed profiles can be described by a multi-domain model rather than a mono-domain model. The nano-meter-sized domain is agitated by thermal fluctuations and eventually ruptured, which may result in the multi-domain state. The kinetically trapped nano-meter-sized domains grow to a mono-domain state by decreasing temperature. Furthermore, between the miscibility and disorder-order transition temperature of saturated lipid, the integrated SANS intensity increased slightly, indicating the formation of nano-meter-sized heterogeneity prior to the domain nucleation.     

Film formation from latex: Hindered initial interdiffusion of constrained polystyrene chains characterized by small-angle neutron scattering

Bulk polystyrene film samples were made from a 50% deuterated latex with a molecular weight of 5.85 × 10⁶ g/mol and 38 nm particle diameter. Because of the high molecular weight and small particle size, these chains are constrained in dimensions by a factor of four. Mildly molded (compacted to full density) samples were annealed for increasing time periods and their small-angle neutron scattering (SANS) patterns recorded. The radii of gyration increase with time as segmental diffusion proceeds during film formation. The initial diffusion was hindered, as shown by a slower than expected relaxation of the chains. Residual interfacial effects were postulated to be the main cause. Chain interdiffusion between latexes of about 110 Å is sufficient to develop a tough, coherent film.     

The frozen state in the liquid phase of side-chain liquid-crystal polymers

Quenched isotropic melts of side-chain liquid-crystal polymers reveal surprisingly an anisotropic polymer conformation. This small-angle neutron-scattering (SANS) result is consistent with the identification of a macroscopic, solidlike response in the isotropic phase. Both experiments (rheology and SANS) indicate that the polymer system appears frozen on millimeter length scales and at the time scales of the observation. This result implies that the flow behavior is not the terminal behavior and that cross-links or entanglements are not a necessary condition to provide elasticity in melts.     

Transition from unilamellar to bilamellar vesicles induced by an amphiphilic biopolymer

We report some unusual structural transitions upon the addition of an amphiphilic biopolymer to unilamellar surfactant vesicles. The polymer is a hydrophobically modified chitosan and it embeds its hydrophobes in vesicle bilayers. We study vesicle-polymer mixtures using small-angle neutron scattering (SANS) and cryotransmission electron microscopy (cryo-TEM). When low amounts of the polymer are added to unilamellar vesicles of ca. 120 nm diameter, the vesicle size decreases by about 50%. Upon further addition of polymer, lamellar peaks are observed in the SANS spectra at high scattering vectors. We show that these spectra correspond to a co-existence of unilamellar and bilamellar vesicles. The transition to bilamellar vesicles as well as the changes in unilamellar vesicle size are further confirmed by cryo-TEM. A mechanism for the polymer-induced transitions in vesicle morphology is proposed.     

Liquid–gas critical phenomena under confinement: small-angle neutron scattering studies of CO2 in aerogel

Small angle neutron scattering (SANS) is a well-established technique for investigating the behavior of confined binary liquid solutions, as it can probe the correlation length and susceptibility in pores on length scales 1 – 100 nm. We applied SANS to explore the influence of confinement on critical behavior of an individual fluid carbon dioxide (CO₂) in a highly porous aerogel. The results demonstrate that quenched disorder induced by aerogel significantly depresses density fluctuations. Despite the negligible volume occupied by aerogel (< 4%), the macroscopic phase separation of confined CO₂ into coexisting liquid and gaseous phases is suppressed and below the critical temperature of the bulk fluid frozen methastable microdomains are formed. Experimental data show that critical adsorption is as important as the effect of confinement in defining the behavior of confined fluids.     

Elasticity effects on domain coarsening of the lamellar-gyroid transition observed in a nonionic surfactant system

The coarsening process of the gyroid phase of a nonionic surfactant system is investigated by time resolved small angle neutron scattering (SANS) and small angle neutron Laue diffraction techniques. The time evolution of SANS patterns shows anomalous coarsening of the gyroid domains. The observed Laue spot from a gyroid domain becomes elongated along the radial direction with the elapse of time and at a certain time the elongated spot is split into two spots. The results can be interpreted as follows. During the coarsening process, mismatch of the lattice orientation at the domain boundary brings strong stress to the gyroid domain, resulting in the distortion of the domain. The stored stress in the domain finally brings splitting of the gyroid domain. The elastic and fragile nature of the gyroid domains composed of the "soft matter" is responsible for the anomalous coarsening.     

Small angle neutron scattering observation of chain retraction after a large step deformation

The process of retraction in entangled linear chains after a fast nonlinear stretch was detected from time-resolved but quenched small angle neutron scattering (SANS) experiments on long, well-entangled polyisoprene chains. The statically obtained SANS data cover the relevant time regime for retraction, and they provide a direct, microscopic verification of this nonlinear process as predicted by the tube model. Clear, quantitative agreement is found with recent theories of contour length fluctuations and convective constraint release, using parameters obtained mainly from linear rheology. The theory captures the full range of scattering vectors once the crossover to fluctuations on length scales below the tube diameter is accounted for.     

Characterization of Nanoparticles and Colloids in Aquatic Systems 1. Small Angle Neutron Scattering Investigations of Suwannee River Fulvic Acid Aggregates in Aqueous Solutions

Fulvic acids (FA) and humic acids (HA) constitute 30–50% of dissolved organic matter in natural aquatic systems. In aqueous solutions, a commonly accepted view is that FA and HA exist as soluble macroligands at low concentration and as supramolecular aggregates at higher concentration. The size, shape and structure of these aggregates are still the subject of ongoing debate in the environmental chemistry literature. In this article, we use small angle neutron scattering (SANS) to assess the effects of solute concentration, solution pH and background electrolyte (NaCl) concentration on the structures of Suwannee River FA (SRFA) aggregates in D₂O. The qualitative features of the SANS curves and data analysis are not consistent with the view point that SRFA forms micelle-like aggregates as its concentration in aqueous solution increases. We find that SRFA forms fractal aggregates in D₂0 with size greater than 242 nm. The SRFA aggregates undergo a significant degree of restructuring in compactness as solution pH, solute concentration and NaCl concentration increase.     

Recent developments and projects in SANS instrumentation at LLB-Orphée

This article presents an overview of the recent developments in SANS and GISANS instrumentation at LLB-Orphée. SANS is a well-known technique, especially well adapted for research in material sciences, soft matter and nanosciences, which has proved to be particularly powerful to study complex systems, from nm to ??m, taking full advantage of isotopic labelling and contrast variation methods. In this article, two instruments will be described in some details: TPA, the new VSANS (Very-Small Angle Neutron Scattering) instrument which is now fully functional and PA20, the new SANS spectrometer under construction, which will extend LLB??s capabilities in terms of SANS for magnetism with a polarized neutron option and Grazing Incidence SANS (GISANS).     

Form-factors for different aggregation models of micelles

Spherical micelles in ionic micellar solutions, often aggregate to form spherical, cylindrical or chain-like aggregates on addition of salt to the solution. It is known that the technique of small angle neutron scattering (SANS) can be used to distinguish spherical and cylindrical aggregates. To examine if SANS can be used to distinguish the latter two aggregation processes, we have calculated the angular distribution of scattered neutrons from 0.002 M CTAB solutions. These calculations show that aggregation of CTAB micelles results in large changes in SANS spectra. The shapes of SANS spectra are different for the above three types of aggregates, suggesting that technique of SANS can indeed be used to distinguish the three aggregation processes. The size of the aggregate can also be obtained from such studies.     

Time-resolved nuclear spin-dependent small-angle neutron scattering from polarised proton domains in deuterated solutions

We have investigated the process of dynamic proton polarisation by means of time-resolved polarised small-angle neutron scattering (SANS) on frozen solutions of EHBA-Cr^V molecules in glycerol-water mixtures as a function of the concentration of EHBA-Cr^V and for different degrees of deuteration of the solvent. In the EHBA-Cr^V complex, the spins of the 20 protons which surround the paramagnetic Cr^V can be oriented using the method of dynamic nuclear polarisation (DNP), thereby offering the possibility to create locally a nuclear spin-dependent contrast for SANS. The time constants which describe the build-up of polarisation around the paramagnetic centre and the subsequent diffusion of polarisation in the solvent were determined by analysing the temporal evolution of the nuclear polarisation, which in turn was obtained by fitting a core-shell model to the time-dependent SANS curves. The results on the spin dynamics obtained using the scattering function of a core-shell could be independently confirmed by evaluating the integrated SANS intensity. A thermodynamic one-centre model is presented which is able to reproduce the observed dependence of the proton polarisation times on the proton concentration of the solvent.