Solubility analysis of clozapine and lamotrigine in supercritical carbon dioxide using static system

The experimental techniques used to obtain the solubilities of clozapine and lamotrigine in supercritical carbon dioxide include a simple static technique. The solubility measurements were performed at temperatures between 318 and 348 K and pressures between 121.6 and 354.0 bar. These chemicals have solubilities with values ranging from 3.6 × 10⁻⁶ to 4.2 × 10⁻⁵ (clozapine) and 1 × 10⁻⁶ to 6 × 10⁻⁵ (lamotrigine) mole fraction. The solubility data were correlated using four semi-empirical density-based models (Chrastil, Bartle, K-J and M-T models). Correlation of the results shows good self-consistency of the data obtained with the Bartle model for clozapine with an overall average absolute relative deviation (AARD%) of 11.21. The calculated results with each four models show satisfactory agreement with the experimental data for lamotrigine with an overall AARD% 11.72, 8.99, 2.75, 3.86 for Chrastil, K-J, Bartle, M-T models, respectively. Using the correlation results, the heat of drug-CO₂ solvation and that of drug vaporization were approximated.     

The effect of sodium dodecyl sulfate on mean drop size in a horizontal mixer–settler extractor

The effects of surfactant concentration, impeller speed, and holdup on mean drop diameter, D₃₂, during emulsification have been studied in a mixer–settler. Two well‐defined regions for the dependence of D₃₂ on surfactant concentration were observed. At low surfactant concentrations, D₃₂ decreased significantly with an increase in surfactant concentration, whereas D₃₂ did not depend on surfactant concentration at high surfactant concentrations. The decreasing rate of change of D₃₂ with impeller speed and the increasing rate of change of D₃₂ with holdup both decreased when a surfactant was added to the system. Moreover, an empirical correlation has been derived to predict D₃₂.     

Modeling permeability of 3-D nanofiber media in slip flow regime

Over the last few decades, numerous analytical and/or numerical expressions have been developed for predicting the permeability of a fibrous medium. These expressions, however, are not accurate in predicting the permeability of media made up of nanofibers. This is because the previous expressions were mostly developed for coarse fibers, where using the so-called no-slip velocity boundary condition at the fiber surface is quite justified. Removing the no-slip velocity restriction in this work, we study the effect of slip flow on the permeability of fibrous materials made up of nanofibers. This has been accomplished by generating a large series of 3-D virtual geometries that resemble the microstructure of a nanofiber (e.g., electrospun) material. Stokes flow equations are solved numerically in the void space between the nanofibers, with the slip flow boundary condition developed based on the Maxwell first order model. The influence of fiber diameter and solid volume fraction (SVF) on the media's permeability is studied, and used to establish a correction factor for the existing permeability expressions when used for nanofiber media.     

Fabrication of Sub‐10 nm Metallic Lines of Low Line‐Width Roughness by Hydrogen Reduction of Patterned Metal–Organic Materials

The fabrication of very narrow metal lines by the lift‐off technique, especially below sub‐10 nm, is challenging due to thinner resist requirements in order to achieve the lithographic resolution. At such small length scales, when the grain size becomes comparable with the line‐width, the built‐in stress in the metal film can cause a break to occur at a grain boundary. Moreover, the line‐width roughness (LWR) from the patterned resist can result in deposited metal lines with a very high LWR, leading to an adverse change in device characteristics. Here a new approach that is not based on the lift‐off technique but rather on low temperature hydrogen reduction of electron‐beam patterned metal naphthenates is demonstrated. This not only enables the fabrication of sub‐10 nm metal lines of good integrity, but also of low LWR, below the limit of 3.2 nm discussed in the International Technology Roadmap for Semiconductors. Using this method, sub‐10 nm nickel wires are obtained by reducing patterned nickel naphthenate lines in a hydrogen‐rich atmosphere at 500 °C for 1 h. The LWR (i.e., 3 σ_LWR) of these nickel nanolines was found to be 2.9 nm. The technique is general and is likely to be suitable for fabrication of nanostructures of most commonly used metals (and their alloys), such as iron, cobalt, nickel, copper, tungsten, molybdenum, and so on, from their respective metal–organic compounds.     

Influence of Ultrasonic Waves on the Processing of Cotton with Cationic Softener

In recent years, the textile industry has been forced to develop new technologies to reduce energy and water consumption. The use of ultrasound in textile wet processing is one solution to this problem. The aim of this work was to investigate the effects of ultrasonic energy on the processing of cotton with a cationic softener. For this purpose, cotton fabric was treated with a fatty acid amide derivative cationic softener in water using ultrasonic energy during treatment. The physical properties of the fabrics treated under different conditions are discussed. The results show that the treatment of fabrics with softeners in an ultrasound bath is more effective compared to conventional methods and that it enhances the physical properties of the cotton.     

Frying performance of the hull oil unsaponifiable matter of Pistacia atlantica subsp. mutica

The anti‐rancidity effect of the hull oil unsaponifiable matter (USM, 100 ppm) of Pistacia atlantica subsp. mutica (Bene) on sunflower oil (SFO) during frying at 180 °C was investigated and compared to that of tert‐butylhydroquinone (TBHQ, 100 ppm). The unsaponifiable constituents of the Bene hull oil (BHO) were separated into hydrocarbons (3.7%), carotenes (3.6%), tocopherols and tocotrienols (24.7%), linear and triterpenic alcohols (0.9%), methylsterols (5.7%), sterols (3.2%), triterpenic dialcohols (4.7%), and triterpenic dialcohol methylesters (4.5%), by means of silica gel TLC. The results obtained from the measurements of total polar compounds, conjugated diene value, carbonyl value, and acid value during 32 h of frying showed that the frying stability of SFO improves more in the presence of the USM of BHO than in the presence of TBHQ. Moreover, compared to TBHQ, the USM had a better protective effect on the indigenous tocopherols of SFO during frying.     

Helical metallomacrocyclic nickel(II) complexes of a tetradentate N2S2 ligand derived from N-methyldithiocarbazic acid

The structure of the tetradentate sulphur–nitrogen chelating agent, 1,2-phenylenebis(methylene) bis(1-methylhydrazinecarbodithioate) (NSSN) has been determined by X-ray diffraction. In the solid state, the two arms of the ligand remain in E configurations about the hydrazinic C–N bonds. The ligand reacts with hydrated nickel(II) salts in a 3:2 ligand-to-metal ratio yielding dimeric triple helical complexes of general formula, [Ni₂(NSSN)₃]X₄·nH₂O (X = Cl, Br, I, NCS; n = 5, 6, 9) which contain two nickel(II) ions in distorted octahedral environments. An X-ray crystallographic structure determination of the [Ni₂(NSSN)₃]Cl₄·9H₂O complex shows that it is a metallomacrocycle in which each ligand acts as a bis-bidentate chelating agent providing NS donors of one arm to one nickel(II) ion and NS donors of the second arm to a second nickel(II) ion. Each nickel(II) ion adopts a distorted octahedral geometry with a NiN₃S₃ coordination core as shown by their common electronic spectra.     

Hydrolytic Depolymerization of PET in a Microwave Reactor

Recycling of PET was examined using hydrolytic depolymerization in an alkaline solution under microwave irradiation. The reaction was carried out in a sealed microwave reactor in which the pressure and temperature were controlled and recorded. The main products were the monomers TPA and EG. The effect of reaction temperature, time, amount of PET and alkaline concentration on the degree of PET depolymerization and TPA recovery was investigated. Microwave irradiation was found to reduce the time needed to achieve a specific degradation of PET significantly, with almost complete depolymerization occurring in 30 min at 180 °C and only 46 W of microwave power. Using a phase transfer catalyst (TOMAB) resulted in the same amount of unreacted PET but at significantly lower depolymerization temperatures.

     

One‐Pot Thioetherification of Aryl Halides Using Thiourea and Alkyl Bromides Catalyzed by Copper(I) Iodide Free from Foul‐Smelling Thiols in Wet Polyethylene Glycol (PEG 200)

In this article, we have developed a new protocol for the thioarylation of structurally diverse alkyl bromides such as benzyl, cinnamyl, n‐octyl, cyclohexyl, cyclopentyl, and tert‐butyl bromides with aryl iodides, bromides and an activated chloride using thiourea catalyzed by copper(I) iodide in wet polyethylene glycol (PEG 200) as an eco‐friendly medium in the presence of potassium carbonate at 80 and 100 °C under an inert atmosphere. The process is free from foul‐smelling thiols which makes this method more practical for the thioetherification of aryl halides. Another important feature of this method is the variety of alkyl bromides which are commercially available for the in situ generation of thiolate ions with respect to the existing protocols in which the less commercially available thiols are directly used for the preparation of arylthio ethers.     

Enhancement of stack ventilation in hot and humid climate using a combination of roof solar collector and vertical stack

In the hot and humid climate, stack ventilation is inefficient due to small temperature difference between the inside and outside of naturally ventilated buildings. Hence, solar induced ventilation is a feasible alternative in enhancing the stack ventilation. This paper aims to investigate the effectiveness of a proposed solar induced ventilation strategy, which combines a roof solar collector and a vertical stack, in enhancing the stack ventilation performance in the hot and humid climate. The methodology selected for the investigation is physical experimental modelling which was carried out in the actual environment. The results are presented and discussed in terms of two performance variables: air temperature and air velocity. The findings indicate that the proposed strategy is able to enhance the stack ventilation, both in semi-clear sky and overcast sky conditions. The highest air temperature difference between the air inside the stack and the ambient air (T_i−T_o) is achieved in the semi-clear sky condition, which is about 9.9 °C (45.8 °C–35.9 °C). Meanwhile, in the overcast sky condition, the highest air temperature difference (T_i−T_o) is 6.2 °C (39.3 °C–33.1 °C). The experimental results also indicate good agreement with the theoretical results for the glass temperature, the air temperature in the roof solar collector’s channel and the absorber temperature. The findings also show that wind has significant effect to the induced air velocity by the proposed strategy.