Effect Of Solvent Evaporation Rate Research Articles

Solubility and Crystallization of Piroxicam from Different Solvents in Evaporative and Cooling Crystallization

In this work, the solubility of a non-steroidal anti-inflammatory drug (NSAID), piroxicam, is investigated. The polymorphic form II, which is the most stable form at room temperature, was investigated in seven different solvents with various polarities. It has been found that the solubility of piroxicam in the solvents is in the following order: chloroform > dichloromethane > acetone > ethyl acetate > acetonitrile > acetic acid > methanol > hexane. Crystallization of piroxicam from different solvents has been performed with evaporative crystallization and cooling crystallization; the effects of solvent evaporation rate and solute concentration have also been studied. Both form I and form II could be produced in cooling and evaporative crystallization, and no simple link can be identified between the operating parameters and the polymorphic outcome. Results obtained in the present work showed the stochastic nature of the nucleation of different polymorphs as well as the complexity of the crystallization of a polymorphic system.

溶液含浸木材の養生過程における細胞壁への溶質拡散に及ぼす溶媒蒸発速度の影響

溶液含浸木材の養生過程における細胞壁への溶質拡散に及ぼす溶媒蒸発速度の影響

Effects of Solvent Evaporation Rate and Poly(acrylic acid) on Formation of Poly(ethylene oxide)-block-polystyrene Micelles from Emulsion

In this work, a solution of poly(ethylene oxide)-block-polystyrene (PEO-b-PS) block copolymer in an organic solvent was dispersed in water to form an emulsion in the presence of poly(acrylic acid) (PAA), which upon solvent evaporation produced micelles, and the “emulsion and solvent evaporation” process was studied. It was found that PAA interacted with the PEO corona of the micelles to reduce the curvature, transforming the aggregates from cylinders into vesicles when 1,2-dichloroethane was the solvent. However, when a more volatile solvent, dichloromethane, was used instead, cylindrical micelles were obtained. Even from 1,2-dichloroethane, cylinders were the predominant species when the initial solution concentration was higher (i.e., shorter evaporation process) or when PAA with a much higher molecular weight was used. On the basis of these observations, the interplay between the solvent evaporation rate and the mass transport and chain reorganization at the interface is discussed. In addition, some in...

Effect of Solvent Evaporation Rate on Order-to-Disorder Phase Transition Behavior of Regioregular Poly(3-butylthiophene)

The effect of solvent evaporation rate on the crystal modification and the thermal stability of solution cast regioregular poly(3-butylthiophene) (P3BT) film was investigated by WAXD, DSC, and FTIR. It is found that, independent of the solvent evaporation rates, the P3BT films prepared from chloroform solution demonstrate essentially the same interlayer distance, which is very close to the reported value of form I′, rather than the conventional form I. However, in the DSC heating curves, it is interesting to find that a single “melting” peak and a double one in the temperature region of 45–100 °C can be observed respectively for P3BT films prepared with fast and extremely slow solvent evaporation rates. The double melting behavior of P3BT in this low-temperature region has never been discussed in the literature. By temperature-dependent infrared spectroscopy, it is shown that these low-temperature “melting” peaks are related to the order-to-disorder phase transition (form I′ to form I) of P3BT. Furthermor...

Solvent and substrate effects on inkjet-printed dots and lines of silver nanoparticle colloids

The shape changes of inkjet-printed dots and lines were investigated by varying the primary solvent of nanosilver colloids, surface wettability and substrate temperature. The morphological changes in dots and lines in array patterns due to the interaction between neighboring dots or lines during evaporation was also examined for two different nanosilver colloids. In order to examine the effect of solvent evaporation rate, two different solvents with different boiling points (BP) were employed for nanosilver inks. With a fluorocarbon film coating and subsequent ultraviolet ozone (UV/O3) treatment, various surface wettability conditions were obtained on silicon (Si) wafers. Substrate temperature was varied from room temperature to 80 °C, and droplets from a 50 µm diameter nozzle were printed onto the substrate after optimizing the ejection of individual droplets. The results indicate that the shapes and sizes of dots and lines are sensitive to changes in both surface energy and substrate temperature, and the ink with a higher BP solvent produces larger dots under the same surface condition due to its slower evaporation. Dots and lines with better quality are achieved using the ink with a lower BP solvent. The morphological changes in dot and line arrays are dependent on the evaporation rate of the primary solvent as well as the distance between neighboring features. As a result, selecting a proper solvent for nanosilver ink is very crucial for controlling the shape and morphology of inkjet-printed patterns.

Effect of solvent evaporation rate on the crystalline state of electrospun Nylon 6

The role of solvent evaporation on the crystalline state of electrospun Nylon 6 fibers was examined by electrospinning into a closed chamber filled with different concentrations of solvent vapor. It was found that the thermodynamically stable α form became increasingly dominant in Nylon 6 fibers electrospun out of both 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and formic acid as the vapor phase solvent concentration increased. It is believed that the formation of the metastable γ form is due in part to the fast solvent evaporation kinetics associated with the electrospinning process. By varying the vapor phase concentration and thus the rate of solvent evaporation during electrospinning, we were able to vary the resulting crystal structure of the electrospun Nylon 6, as shown by XRD, Raman and FTIR.

Morphology and Phase Segregation of Spin-Casted Films of Polyfluorene/PCBM Blends

In this study the morphology of spin-casted films of polymers blended with [6,6]-phenyl C61-butyric acid methyl ester (PCBM) has been studied. It was found that the lateral structure formation in the films is favored by rapid solvent evaporation and strong polymer−PCBM repulsion. The formation of homogeneous films is favored by slow evaporation and weak polymer−PCBM repulsion. The effect of solvent evaporation rate is the opposite of what is found for spin-casting polymer−polymer blends. The results can be explained by the kinetics of phase separation and the phase behavior involving limited solubility and crystallization of PCBM.

Effect of temperature-increase rate on drug release characteristics of dextran microspheres prepared by emulsion solvent evaporation process

Microspheres containing theophylline (TH) were prepared from a hydrophobic dextran derivative by an emulsion solvent evaporation process using an acetone/liquid paraffin system. The effects of solvent evaporation rate on particle properties and drug release characteristic of the microspheres were evaluated. The solvent evaporation rate was controlled by the rate of increase in temperature of the water bath, ranging 7.5–30 °C/h. Drug release from the microspheres was examined using JPXIV 2nd fluid (pH 6.8) containing 0.1% Tween 80, and was found to be greatly affected by the solvent evaporation rate. The percentage of drug released until 8 h varied; from 28% to 84% for 30 and 7.5 °C, respectively. Differential scanning calorimetry and powder X-ray diffraction studies revealed that TH partially interacted with the polymer and drug crystallinity was maintained intact in the microspheres. According to scanning electron microscopy observations, all microspheres showed a well-formed spherical particle with a solid interior. The appearances of the microspheres were, however, extremely different. Microspheres prepared at 30 °C/h had a very smooth surface, while those prepared at 7.5–15 °C/h had a rough surface with large craters. These findings demonstrated that the surface morphology and drug release characteristic were controlled by the rate of increase of temperature.

Effects of solvent evaporation rate on the properties of protein-loaded PLLA and PDLLA microspheres fabricated by emulsion-solvent evaporation process

This paper investigated the effects of the rate of solvent removal by varying the ambient pressure at a fixed temperature on the morphology, particle size, encapsulation efficiency and release pattern of albumin-loaded PLLA and PDLLA microspheres, prepared by the W/O/W emulsion-solvent evaporation process. For PLLA microspheres prepared either with a fast rate of solvent evaporation (FRSE) or a normal rate of solvent evaporation (NRSE) process, the difference in morphology was minor. In contrast, the different processes did affect the morphology of PDLLA microspheres. Large (surface) pores were observed for PDLLA microspheres fabricated with a FRSE process, while a smooth surface was seen in those with a NRSE process. With the FRSE process, both PLLA and PDLLA microspheres showed smaller particle sizes and lower albumin encapsulation efficiencies than those prepared in the NRSE process. PLLA microspheres prepared with the NRSE process had higher drug encapsulation efficiencies than PDLLA ones, but this was not the case for the FRSE process. An initial burst release of albumin was observed for both PLLA and PDLLA microspheres prepared with the NRSE process, while a lesser burst release was seen for those prepared with the FRSE process. In subsequent stages of drug release, PLLA microspheres prepared with the two different processes showed differences, but this was not the case for PDLLA ones.

Effect of solvent evaporation rate on surface composition in fluoro‐copolymer/acrylate‐copolymer blend films

AbstractThe relationship between the surface composition and the rate of solvent evaporation (R) in blend films of poly(vinylidene fluoride‐co‐hexafluoroacetone) (P(VDF‐HFA)) and poly(2‐ethylhexyl acrylate‐co‐acrylic acid‐co‐vinyl acetate) (P(2EHA‐AA‐VAc)) has been investigated. P(VDF‐HFA), a low‐surface tension component, was concentrated on the surface when R was relatively high. In contrast, when R was relatively low, P(2EHA‐AA‐VAc), a low‐density component, was concentrated on the surface. Therefore, it is speculated that the factors dominating surface enrichment in polymer blends were changed from surface tension differences to density differences between the components when R was decreased. In addition, the affinity between components and substrate strongly affects the dominant factors determining the surface composition.© 2001 Society of Chemical Industry

Fabrication of porous poly(?-caprolactone) microparticles for protein release

The particle morphology and in vitro release of protein from porous and non-porous PCL-F127 blended microparticles were evaluated. The BSA loaded PCL microparticles were prepared by the w/o/o/o emulsion-solvent evaporation method. Two types of homogenizer, a Polytron® homogenizer and a probe ultrasonicator, were used to prepare the emulsion systems. The effects of solvent evaporation rate on the crystallinity and the performance of the microparticles were investigated. Both microparticles showed quite different shapes as well as surface morphology and release characteristics. The microparticles prepared with a Polytron® homogenizer were quite porous in structure, which created channels for protein to continuously diffuse out, and resulted in sustained- and controlled-release characteristics. In addition, the initial burst release of protein from the microparticles was also reduced. Alteration of the evaporation rate of solvent did not change the crystallinity of the final microparticles. An influence of evaporation rate on the size of resulting microparticles was observed. The porous PCL microparticles were developed by choosing a proper homogenizer and fabrication conditions. Carefully controlling these variables resulted in microparticles with desirable release performance.

Morphological transformations in solution-cast Styrene-Butadiene-Styrene (SBS) triblock copolymer thin films

The fact that block copolymers can assume a range of morphologies depending upon such variables as relative block length and molecular weight is now well known. In the case of poly(styrene)[PS]-poly(butadiene)[PB]-poly(styrene) (SBS) triblock copolymer, the morphologies range from spheres (roughly ~20% minor component), to cylinders (roughly 20%~35% minor component), to lamellae (roughly equal component fractions) Most recently, there has been increasing interest in transformations between morphologies by thermal annealing. This paper describes initial results studying the effect of solvent evaporation rate and post-casting annealing treatment on the morphology of SBS thin films.TEM specimens were prepared by solution casting electron transparent films. 50 μl of 0.1 wt% SBS (30% styrene, Mw=14,000, Scientific Polymer Products, Inc.) dissolved in toluene was deposited on a polished NaCl single crystal substrate placed in a small dish. After solvent evaporation the film was cut into small squares, floated from the salt in water, and each square was collected on a Cu grid.

スチンレン系熱可塑性エラストマー／選択溶媒系のキャスト法成膜における溶媒蒸発速度の影響

スチンレン系熱可塑性エラストマー／選択溶媒系のキャスト法成膜における溶媒蒸発速度の影響

Effect of solvent evaporation rate on microphase‐separated structure of segmented poly(urethane‐urea) prepared by solution casting

AbstractA useful instrument for polymer film preparation by solution casting was employed in this study. It enabled us to control the solvent evaporation rate of the polymer solution. By using this instrument, the aggregation of hard segments in segmented poly(urethane‐urea) (SPUU) was investigated. SPUU was prepared from poly(tetramethy1ene oxide), 4,4′‐diphenylmethane diisocyanate and ethylenediamine. The effect of solvent evaporation rate on the microphase‐separated structure of SPUU was elucidated by dynamic mechanical analysis, tensile test, differential scanning calorimetry analysis, small‐angle X‐ray scattering measurement, IR and IR dichroism analyses. The aggregation of hard segments in SPUU was observed to be affected considerably by the solvent evaporation rate of the cast film during the preparation. It was found that the slower the solvent evaporation rate, the higher the aggregation of hard segments to form rigid hard segment domains in SPUU. Nine months after casting, this casting effect still remained on the aggregation state of hard segments of SPUU films, although the interdomain spacing was not influenced by its rate.