Dissolution kinetics of dehydroxylated nickeliferous goethite from limonitic lateritic nickel ore

The dissolution kinetics in 2 M H₂SO₄ of variously dehydroxylated nickeliferous goethites was investigated for five oxide-type lateritic nickel deposits. Goethite was the main constituent with minor amounts of quartz, talc, kaolinite and Mn oxides. Dissolution of Fe from heated materials followed the Kabai equation. There was a 9–34-fold increase in the Kabai dissolution rate constant (k) for samples heated at 340–400 °C due to both the increased surface area (1.5–2.6 fold) and higher density of structural defects (5–10 fold) in the variously dehydroxylated products. The presence of structural Al and Cr in goethite appears to reduce dissolution rate possibly through the greater M³⁺–OH, O bond strength relative to Fe³⁺, Ni²⁺–OH, O. Nickel showed congruent dissolution with Fe indicating that Ni was uniformly incorporated in the goethite structure. Pre-heating goethite to 600–800 °C for 30 min resulted in incongruent dissolution of Fe and Ni. It is postulated that some Ni is ejected from the neo-formed hematite structure and resides on the crystal surface or in voids. These results may contribute to the development of more efficient procedures for Ni extraction including heap leaching of lateritic nickel ores.     

家蚕蛹甲壳素的H_2O_2脱色及冷冻溶解研究

用4%H2O2溶液在pH11和温度75℃条件下对蚕蛹甲壳素进行漂白,能获得理想的白度(66.5)。以8%NaOH/10%Urea为混合溶剂,冷冻溶解脱色甲壳素。结果表明:脱色甲壳素白度越高溶解度越高;冷冻温度在-20℃及以下,溶剂中水分子才能结晶并破坏甲壳素结晶结构;而且溶剂体系为NaOH/Urea水溶液时最好,添加有机相(如乙醇、丙酮、DMSO)会使甲壳素溶解率下降甚至不溶。     

Solid dispersions of diflunisal-PVP: polymorphic and amorphous states of the drug

Coprecipitates of diflunisal and polyvinylpyrrolidone (PVP K15, K30, and K90) and physical mixtures were studied using x-ray diffraction analysis, infrared (IR) spectroscopy, differential scanning calorimetry (DSC), and hot-stage microscopy. X-ray diffraction results revealed an almost amorphous state, even in coprecipitates with a high content of drug, next to 70%, which was independent of the polymer molecular weight. The IR spectra of 70:30 drug-PVP solid dispersions suggest the formation of diflunisal-PVP hydrogen bonds. For 70:30 drug-polymer ratio, the physical mixture showed linear dissolution kinetics of free crystals, but the corresponding coprecipitates exhibit two different dissolution processes. When the 25:75 drug-polymer dispersion is analyzed by hot-stage microscopy, only solid plates of PVP are observed; the absence of drug particles may be due to a molecular dispersion of the drug into the polymer. Moreover, polymorphic changes of diflunisal were detected in the solid dispersions in comparison with the corresponding physical mixtures, which are always formed by polymorph II. At high concentrations of drug (75:25 and 80:20), x-ray diffraction patterns of solid dispersions showed the partial recrystallization of the drug, displaying the main diffraction peaks of polymorph I when ethanol was used as coprecipitation solvent, whereas diflunisal form IV was obtained in chloroform.     

Dissolution behavior of Cu and Ag substrates in molten solders

This study investigated the dissolution behavior of Cu and Ag substrates in molten Sn, Sn-3.5Ag, Sn-4.0Ag-0.5Cu, Sn-8.6Zn and Sn-8.55Zn-0.5Ag-0.1Al-0.5Ga lead-free solders as well as in Sn-37Pb solder for comparison at 300, 350, and 400°C. Results show that Sn-Zn alloys have a substantially lower dissolution rate of both Cu and Ag substrates than the other solders. Differences in interfacial intermetallic compounds formed during reaction and the morphology of these compounds strongly affected the substrate dissolution behavior. Soldering temperature and the corresponding solubility limit of the substrate elements in the liquid solder also played important roles in the interfacial morphology and dissolution rate of substrate.     

In vitro-in vivo correlation and comparative bioavailablity of vincamine in prolonged-release preparations

Developing an in vitro dissolution test that gives good correlation with in vivo data for a particular drug product is an important objective. Available dissolution data of vincamine prolonged-release preparations show different in vitro release behavior at different pH using the conventional dissolution techniques. This does not allow development of an in vitro-in vivo correlation (IVIVC). In the present work, the flow-through cell (FTC) dissolution system (USP apparatus 4) was utilized to compare the release rate of three marketed prolonged-release oral formulations of vincamine; namely, a brand innovator formulation used as the reference and two formulations from different manufacturers as test products. Both the open and closed systems of FTC were used at variable pH. A comparative bioavailability study was then conducted in 16 healthy volunteers for a test versus the reference product by administering a single dose of 60 mg in a crossover design. Vincamine plasma concentrations were analyzed by a sensitive high-performance liquid chromatography (HPLC) method. This was followed by assessment of IVIVC according to level A as specified by USP 23; the absorbed fraction of vincamine was determined using the Wagner-Nelson method. The results indicated that the pH of the medium affects the release rate pronouncedly. The relative bioavailability based on C_max and AUC_0-12 were found to be 83.15% and 84.15%, respectively. Good correlation was obtained between fraction absorbed in vivo and fraction dissolved in vitro by applying the open system of the FTC. This technique gave the most favorable results with regard to the percentage vincamine released and the IVIVC     

吸收浓度对玻璃态膜中气体吸收过程影响的研究

通过气体在玻璃态高分子膜中的吸收过程分析,认为在膜中气体分子与膜之间的相互作用将影响吸收等温线。假设气体在膜中的溶解过程类似于在溶液中的溶解过程,推导得出了普遍化双方式吸收模型。该模型中考虑了气体吸收浓度对气体在玻璃态膜中吸收过程的影响,几乎能够描述各种吸收过程。     

Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs

Poor water solubility is an industry wide issue, especially for pharmaceutical scientists in drug discovery and drug development. In recent years, nanoparticle engineering processes have become promising approaches for the enhancement of dissolution rates of poorly water soluble drugs. Nanoparticle engineering enables manufacturing of poorly water soluble drugs into nanoparticles alone, or incorporation with a combination of pharmaceutical excipients. The use of these processes has dramatically improved in vitro dissolution rates and in vivo bioavailabilities of many poorly water soluble drugs. This review highlights several commercially or potentially commercially available nanoparticle engineering processes recently reported in the literature for increasing the dissolution properties of poorly water soluble drugs.     

Evaluation and comparison of five matrix excipients for the controlled release of acrivastine and pseudoephedrine

For treatment of allergic rhinitis, acrivastine with pseudoephedrine in Semprex®-D conventional capsules requires dosing every 6-8 hours. This study was designed to develop a controlled release matrix tablet of acrivastine and pseudoephedrine and evaluate 5 different matrix excipients for their in vitro controlled-release profiles. Compritol® 888ATO, Eudragit® RS, Methocel® K100M, Polyox® WSR301 and Precirol® ATO5 were used alone or in varying combinations for the formulation of controlled release matrix tablets. In vitro drug dissolution and mathematical modeling were used to characterize drug release rate and extent. All tablet formulations yielded quality matrix preparations with satisfactory tableting properties. Due to the aqueous solubility of pseudoephedrine and the size of the dose, none of the matrix excipients used alone prolonged drug release significantly to meet the desired twice-daily administration frequency. The use of two excipients in combination, however, significantly decreased the dissolution rate of both active ingredients. A combined lipid-based Compritol® and hydrophilic Methocel® produced optimal controlled drug release for longer than 8 hours for both acrivastine and pseudoephedrine.     

Experimental investigation of a pilot-scale jet bubbling reactor for wet flue gas desulphurisation

In the present work, an experimental parameter study was conducted in a pilot-scale jet bubbling reactor for wet flue gas desulphurisation (FGD). The pilot plant is downscaled from a limestone-based, gypsum producing full-scale wet FGD plant. Important process parameters, such as slurry pH, inlet flue gas concentration of SO₂, reactor temperature, and slurry concentration of Cl⁻ have been varied. The degree of desulphurisation, residual limestone content of the gypsum, liquid phase concentrations, and solids content of the slurry were measured during the experimental series.The SO₂ removal efficiency increased from 66.1% to 71.5% when the reactor slurry pH was changed from 3.5 to 5.5. Addition of Cl⁻ (in the form of CaCl₂·2H₂O) to the slurry increased the degree of desulphurisation to above 99%, due to the onset of extensive foaming, which substantially increased the gas-liquid contact area. An increase in the inlet flue gas SO₂ concentration from 502 to led to a decrease in the SO₂ removal efficiency from 80.1% to 69.4%. A temperature increase from 296 to caused a reduction in the degree of desulphurisation from 69.4% to 68.1%, but this result is almost within the experimental uncertainty. The residual limestone level in the gypsum formed increased with increasing values of reactor slurry pH, inlet flue gas SO₂ concentration, and slurry concentration of Cl⁻.     

Microwave-accelerated dissolution of MWNT in aniline

Multi-Walled Carbon Nanotube (MWNT), grafted by the carboxylic acid group, was dissolved in aniline rapidly under microwave radiation. The major advantage of this high-energy procedure was that it reduced the whole reaction time to the order of minutes. The dissolution process was completed in two steps and carried out in 30 min under microwave conditions. The MWNT-aniline solution was analyzed by UV-vis spectroscopy and a TEM image of MWNT in aniline was also presented. Moreover, MWNT was studied after dissolution by using Raman spectroscopy and was found that no damage occurred to it.