Colloidal aggregation in polymer blends

We consider here a low-density assembly of colloidal particles immersed in a critical polymer mixture of two chemically incompatible polymers. We assume that, close to the critical point of the free mixture, the colloids prefer to be surrounded by one polymer (critical adsorption). As result, one is assisted to a reversible colloidal aggregation in the nonpreferred phase, due the existence of a long-range attractive Casimir force between particles. This aggregation is a phase transition driving the colloidal system from dilute to dense phases, as the usual gas-liquid transition. We are interested in a quantitative investigation of the phase diagram of the immersed colloids. We suppose that the positions of particles are disordered, and the disorder is quenched and follows a Gaussian distribution. To apprehend the problem, use is made of the standard phi(4) theory, where the field phi represents the composition fluctuation (order parameter), combined with the standard cumulant method. First, we derive the expression of the effective free energy of colloids and show that this is of Flory-Huggins type. Second, we find that the interaction parameter u between colloids is simply a linear combination of the isotherm compressibility and specific heat of the free mixture. Third, with the help of the derived effective free energy, we determine the complete shape of the phase diagram (binodal and spinodal) in the (Psi,u) plane, with Psi as the volume fraction of immersed colloids. The continuous "gas-liquid" transition occurs at some critical point K of coordinates (Psi(c) = 0.5,u(c) = 2). Finally, we emphasize that the present work is a natural extension of that, relative to simple liquid mixtures incorporating colloids.     

Colloidal crystallization in the quasi-two-dimensional induced by electrolyte gradients

We investigated driven crystal formation events in thin layers of sedimented colloidal particles under low salt conditions. Using optical microscopy, we observe particles in a thermodynamically stable colloidal fluid to move radially converging towards cation exchange resin fragments acting as seed particles. When the local particle concentration has become sufficiently large, subsequently crystallization occurs. Brownian dynamics simulations of a 2D system of purely repulsive point-like particles exposed to an attractive potential, yield strikingly similar scenarios, and kinetics of accumulation and micro-structure formation. This offers the possibility of flexibly designing and manufacturing thin colloidal crystals at controlled positions and thus to obtain specific micro-structures not accessible by conventional approaches. We further demonstrate that particle motion is correlated with the existence of a gradient in electrolyte concentration due to the release of electrolyte by the seeds.     

Colloidal aggregation phenomena: Spatial structuring of TEOS-derived silica aerogels

In this contribution, the homogeneity of silica aerogels made from tetraethyl orthosilicate (TEOS) was studied by means of Fourier transform infrared (FTIR) and 29Si nuclear magnetic resonance (NMR) spectroscopies. FTIR spectra show a slight difference in the asymmetric Si-O-Si stretching vibration frequency in the outer and inner part of the aerogels. According to the 29Si NMR data, a higher relation Q4/Q3 was obtained in the inner parts of the gels compared with their outer parts, proving the difference in the cross linkage of the silica network. The obtained results are interpreted in terms of the specific spatial structuring of the colloidal suspensions due to the presence of gravity.     

Complex coacervation core micelles. Colloidal stability and aggregation mechanism

Complex coacervation core micelles were prepared with various polyelectrolytes and oppositely charged diblock copolymers. The diblock copolymers consist of a charged block and a water-soluble neutral block. Our experimental technique was dynamic light scattering in combination with titrations. At mixing ratios where the excess charge of the polyelectrolyte mixture is approximately zero, micelles may be formed. The colloidal stability of these micelles depends on the block lengths of the diblock copolymers and the molecular weight of the homopolymers. In addition, the chemical nature of the corona blocks and nature of the ionic groups of the polyelectrolytes also influence the stability and aggregation mechanism. A corona block that is three times longer than the core block is a prerequisite for stable micelles. If this ratio is further increased, the molecular weight of the homopolymers as well as the type of the ionic groups starts to play a major role. With very asymmetric block length ratios, no micelles are formed. In addition, if the neutral block is too short, the polymeric mixture forms a macroscopic precipitate. With a constant core block, the aggregation number decreases with increasing corona block length, as is predicted by scaling models for polymeric micelles with a neutral corona.     

Polyelectrolyte-surfactant complexes with long range order

Mixtures of carboxymethyl cellulose (CMC) or hydrophobically modified CMC with an oppositely charged surfactant (benzyldimethyltetradecylammonium chloride) in water were prepared. When the global polymer concentration is 0.18% by weight and the surfactant content is high enough, a precipitate with hexagonal order is formed. The precipitate composition shows practically constancy in its water content and a slight diminution in polymer concentration when the global surfactant content is varied between 0.9 and 23 wt%. The lattice parameter in this phase decreases when the polymer/surfactant ratio in the phase increases; this variation is faster with CMC than with the hydrophobically modified CMC. In this way electrostatic and hydrophobic interactions are far from being additive. From the extrapolation to infinite dilution, the global interaction seems to depend on the substitution degree in the polymer. Additionally, the comparison between the radius at the polar-apolar interface in the cylinders and the lattice parameter as a function of polymer/surfactant ratio in the hexagonal phase is compatible with some of the alkyl chains belonging to the hydrophobically modified CMC being present in the aqueous zone.     

Molecular folding induced nanogold aggregation

Bisacridinedione-functionalized gold nanoparticles (bisADD-GNPs) were prepared and characterized. BisADD is a flexible acyclic moiety and a specific Ca²⁺ sensor. Signaling of the binding events is achieved by the cation-induced folding of the bisADD-GNPs and the resultant fluorescence enhancement and visual color change are attributed to the suppression of photoinduced electron transfer (PET) through space and nano-Au aggregation. The selective binding of Ca²⁺ is clear from steady state fluorescence and TEM techniques.     

Rapid aggregation of gold nanoparticles induced by non-cross-linking DNA hybridization

To date, aggregation of DNA-functionalized gold nanoparticles by hybridization of target DNA in a cross-linking configuration has been intensively studied. Here, we report that aggregation in a non-cross-linking configuration is also possible and is even better from the viewpoint of genetic analysis because of its speed and sensitivity. In this system, 15 nm diameter gold nanoparticles functionalized with (alkanethiol)-15mer DNA are hybridized to target 15mer DNA at room temperature. At high NaCl concentration (>/=0.5 M), hybridization with complementary target DNA induces nanoparticle aggregation based on the salting-out effect. The aggregation can be detected by a colorimetric change of the colloidal solution within 3 min. Furthermore, unusual sensitivity of this system for single-base mismatch at the terminus opposite to the anchored side has been discovered. In fact, target DNA with such a kind of mismatch does not induce the colorimetric change at all, while target DNA with single-base mismatch at the middle of it cannot be discriminated from the fully complementary target. This non-cross-linking aggregation system opens up a new possibility of rapid and reliable genetic analysis.     

Directed aggregation and fusion of lipid vesicles induced by DNA-surfactants

We investigated DNA-directed aggregation of vesicles using DNA-surfactants. Following tethering of single-stranded DNA oligonucleotides to vesicles using DNA-surfactant, the tethered vesicles were assembled with other vesicles bearing complementary strands. The vesicle aggregation was strongly affected by the salt concentration and by temperature according to the characteristics of DNA hybridization. Restriction enzyme, which can hydrolyze the double-stranded DNA used in the present study, dissociated the vesicle aggregates. Exploration using fluorescently labeled vesicles suggested that the DNA-directed vesicle aggregation took place in a sequence-specific manner through DNA-duplex formation. Interestingly, the DNA-directed aggregation using short DNA-surfactant induced the fusion of vesicles to produce giant vesicles, resulting in an enzymatic reaction in the giant vesicle.     

Chemical shifts due to long range dispersion interactions

Dispersion chemical shifts, σ_w, for a variety of solute-solvent systems have been obtained by three different methods. The value of σ_w for a given system differs with the method employed for evaluating the characteristic frequency.     

The sequential analysis of long range fallout debris

A method for the determination of the principal radionuelides of Sr, Ba, Ce, Cs, Y, Zr, Nb, and W in single fallout samples containing bulk Si, Fe, and Ca is presented. The sample and added carriers are dissolved by fusion with sodium carbonate. The melt is leached first with hot water and then with hydrochloric acid. W and Cs are recovered from the water leach. Sr, Ba, Y, and the heavier rare earths appear in the hydrochloric acid leach. Ce is found in the leach residue and Nb in both the residue and the hydrochloric acid leach. The Zr and Nb in the residue are separated from Ce by absorption on an anion-exchanger from hydrochloric acid. The Zr and Nb in the hydrochloric acid leach are separated from Sr and Ba by precipitation of Sr and Ba as nitrates and then separated from Y and the heavier rare earths by absorption on the anion-exchanger. The combined Zr fractions are eluted with dilute hydrochloric acid and Nb with a hydrochloric-hydrofluoric acid mixture.     

Unusual emission transformation of graphene quantum dots induced by self-assembled aggregation

Graphene quantum dots prepared by a one-step hydrothermal procedure in a microwave exhibit an unusual emission transformation in strong acidic media and at high concentration, induced by self-assembled J-type aggregation under restrained π-π interactions.     

Light induced aggregation of metal clusters

The influence of light of the Mie plasmon wavelength on the aggregation of 10nm-gold clusters in aqueous colloidal systems is studied by spectral extinction measurements and electron microscopy. The detected significant acceleration of the aggregation process is attributed to additional Van der Waals like forces between the particles. Thermal and photochemical effects are discussed and excluded.     

Characterization of NeNe long range interaction by absolute total cross section measurement

Absolute total elastic cross sections for NeNe collisions have been measured in the 0.5–1.4 km s^?1 velocity range. The analysis of the data allowed accurate characterization of the interaction in a distance range between 3.9 and 5.3 A. This result implements the information previously obtained and improves the knowledge of the Ne₂ interaction potential.     

Pyrrolidine derivatives as inhibitors of platelet aggregation induced by platelet activating factor

Newly synthesized pyrrolidine derivatives inhibited rabbit platelet aggregation induced by platelet activating factor.     

Properties and long range interactions of the calcium atom

The properties of a number of states of calcium are determined from a large basis configuration interaction calculation. The main focus is on the polarizabilities of the low lying states (the 4s2 1Se, 4s3d 1,3De, 4s4p 1,3Po, and 4s5s 1,3Se states) and the dispersion interactions of those states with the calcium ground state, the hydrogen atom, and the rare gases.     

Study of electrolyte induced aggregation of gold nanoparticles capped by amino acids

This work reports the electrolyte induced aggregation of gold nanoparticles directly conjugated to amino acid by chemical reduction in aqueous solution. The study was focused on three different classes of amino acids depending on the nature of alpha substituent, viz. l-cysteine, l-leucine, and l-asparagine. The band broadening and the red shift of surface plasmon band with increase in flocculation parameter showed the aggregation of gold nanoparticles with increase in electrolyte concentration and decrease in pH as monitored by UV-visible spectrophotometer. The (1)H NMR spectrum demonstrates that the sulfide bond of cysteine and alpha amino group of leucine and asparagine interact with nanoparticles surface. Furthermore, transmission electron microscope (TEM) and thermogravimetric analysis (TGA) were performed to characterize and to support the fate of stabilization of the gold nanoparticles by amino acid.     

Analytical interaction potentials of the long range alkali-metal dimers

Using almost degenerate perturbation theory the calculation of long range limits of alkali-metal dimer molecular states which dissociate to the atom pairs S_1/2-P_{1/2, 3/2} and S_1/2-D_{3/2, 5/2} is presented. Hund's coupling casec is adopted. The calculation includes correlations up to the second order of perturbation theory and exchange energy contributions. The results are expressed in a simple analytical form in terms of dispersion coefficients.