Preparation of Ultra-fine Salbutamol Sulfate Particles by Reactive Precipitation and Characterization of Dry Powder Inhalant

The preparation of ultra-fine particles of salbutamol sulphate （SS） was accomplished with a reactive precipitation pathway, in which salbutamol and sulphuric acid were Used as reactants with the solvents of ethanol.The effects of sulphuric acid concentration, reaction temperature, stirring rate, and reaction time onthesize of the particle were investigated. A binary mixture composed of lactose and SS was prepared to evaluate SS. The results showed that ultra-fine SS particles with controlled diameters ranging between 3 μm and 0.8 μm and with a narrow distribution could be achieved. The morphology consisting of clubbed particles wassuccess.fully obtained. The purity of the particles reached above 98% with-UV detection. The dose- of dry powder inhalation was obtained by blending the particles with recrystallized lactose, which acted as a carrier. The deposition quantity of the drug in breathing tract was estimated using a twin imPinger apparatus. Compared with the Shapuer powder （purchased in the market）, the results showed that SS_particles had more quantifies.subsided in simulative lung.. _

Reactive Precipitation of Procaine Benzylpenicillin

The reactive precipitation process of procaine benzylpenicillin is reviewed, while such secondary processes as ageing, agglomeration, breakage, and the effects of operation parameters on crystal size are emphasized. In the reactive precipitation the ageing of particles has a little effect on the process, while the greater effect comes from the agglomeration and breakage of particles, furthermore, the mixing has also notable influence on the product size. All of these provide the bases for further study on reactive precipitation.

MASS PRODUCTION OF NANOPARTICLES BY HIGH GRAVITY REACTIVE PRECIPITATION TECHNOLOGY WITH LOW COST

Mass production of nanoparticles at low cost has attracted much attention from industrial and academic circles. In this paper, a novel method, the high gravity reactive precipitation (HGRP) technology, of manufacturing CaCO3 nanoparticles, presently scaled-up to an annual capacity of 10,000 tons, is presented. This paper describes the process principle, the process design and experiments on the syntheses of 15-30 nm CaCO3, 30-50 nm SiO2, 20-30 nm TiO2, 20-60 nm ZnO, 20-30 nm ZnS, 30 nm SrCO3, 40-70 nm BaTiO3, stick-like nano BaCO3 as well as nano-fibrillar aluminum hydroxide measuring 1-10 nm in diameter and 50-300 nm in length, using liquid-liquid, gas-liquid and gas-liquid-solid reactant systems. The advantage of using the HGRP technology is illustrated by comparison to conventional methods.

Synthesis and Catalytic Activity of Copper(Ⅱ) Resorcylic Acid Nanoparticles

Copper（ Ⅱ ） resercyiic acid（CuRes） nanoparticles were synthesized by using reactive precipitation method with resorcylic acid and blue copperas as the raw material in a rotating packed bed. The sample obtained was characterized by using X-ray diffraction（XRD）, transmission electron micrescopy（TEM）, Fourier transform infrared spectroscopy （FTIR）, thermo-gravimetric analyses （TG）, and element analysis. In addition, the catalytic activity of CuRes nanoparticles on the thermal decomposition of nitrocellulose-nitroglycerine（NC-NG） was also determined via DSC. The results show that the spherical nanoparticles with a diameter of 20 nm were obtained in ethanol solution. The peak temperature of the thermal decomposition of NC-NG-CuRes decreases by 3℃ compared with that of normal CuRes, and the decomposition enthalpy is increased by 735 J/g, and therefore, it is reasonable to assume that CuRes nanoparticles have a better catalytic activity.

Low Temperature One Step Synthesis of Barium Titanate: Particle Formation Mechanism and Large-scale Synthesis

The formation of BaTiO3 nanoparticles via the reaction of BaCl2, TiCl4 and NaOH in aqueous solution has been systematically studied. The formation of BaTiO3 from the ionic precursors has been elucidated to be a very rapid process, occurring at temperature higher than 60℃. Furthermore, the particle size could be controlled by the proper selection of the synthesis conditions (e.g. reactant concentration of 0.5—1.0mol·L-1, temperature of 80— 95℃ and pH≥13). A two-step precipitation mechanism was proposed. The first stage of the synthesis involved the formation of amorphous Ti-rich gel phase. The second stage of the synthesis was the reaction between the amor-phous phase and the solution-based Ba2+ ions, which led to the crystallization of BaTiO3. Based on the particle for-mation mechanism, a novel method, high gravity reactive precipitation, was proposed and used to mass production of BaTiO3 of average particle size of about 60 nm and with narrow particle size distribution. Because it could break up the amorphous Ti-rich gel into small pieces, intensify mass transfer, promote the reaction rate of amorphous Ti-rich gel with Ba2+ ions.

Groundwater fluoride contamination:A reappraisal

Dissolution of fluorite （CaF2） and/or fluorapatite （FAP） [Cas（PO4）3F], pulled by calcite precipitation, is thought to be the dominant mechanism responsible for groundwater fluoride （F） contamination. Here, one dimensional reactive-transport models are developed to test this mechanism using the published dissolution and precipitation rate kinetics for the mineral pair FAP and calcite. Simulation results correctly show positive correlation between the aqueous concentrations of F and CO2 and negative correlation between F- and Ca^2＋. Results also show that precipitation of calcite, contrary to the present understanding, slows down the FAP dissolution by 10G orders of magnitude compared to the FAP dissolution by hydrolysis. For appreciable amount of fluoride contamination rock-water interaction time must be long and of order 106 years.

Effect of Precipitation on Intergranular Corrosion Resistance of 430 Ferritic Stainless Steel

With Nb-Ti-stabilized 430 ferritic stainless steel（NTS430FSS） and SUS 430 ferritic stainless steel（SUS430FSS） as experimental materials, the influence of precipitation on intergranular corrosion resistance was investigated. A series of aging treatment were carried out. The free-exposure corrosion test and double loop electrochemical potentiokinetic reactivation（DL-EPR） test with a scan rate of 1.67 m V/s at 26 °C were applied to evaluate the intergranular corrosion（IGC） resistance. Metallographic observation, scanning electron microscope（SEM）, transmission electron microscope（TEM） with energy dispersive spectroscopy（EDS） and X-ray diffraction（XRD） analysis were conducted. The results show that IGC occurred in SUS430 FSS aged above 700 °C, while it occurred in NTS430 FSS as the temperature was improved to 1 050 °C. The critical degree of sensitization Ir/Ia reaches 0.305 in SUS430 FSS, which is higher than that of NTS430 FSS, i.e. 0.010, aged at 950 °C for 2 h. The TEM, EDS and XRD results show that a large amount of Cr23C6 precipitates with size of 60 nm×22 nm are located at the SUS430 FSS grain boundaries as chains. With the addition of Nb and Ti and reduction of C, the amount of precipitates reduces significantly in NTS430 FSS. A majority of Cr23C6 were replaced by Ti C and Nb C. Only a small amount of spherical Ti C（R=186 nm） and square Ti N（312 nm×192 nm） with Nb and Cr adsorbed are left along grain boundaries. Due to the dual stabilization of Nb and Ti, the precipitation of Cr23C6 is restrained, the chromium depleted region is avoided and accordingly the resistance to the intergranular corrosion is improved.

Reactive poly(divinyl benzene-co-maleic anhydride) nanoparticles:Preparation and characterization

Polymeric nanoparticles（NPs）have drawn great interest in the past few years due to their potential applications in the felds of biomedical and optical technologies.However,it is still a challenge to prepare functional polymeric NPs,especially for particle diameters smaller than 50 nm.In this work,we demonstrate a one-pot method to fabricate reactive poly（divinyl benzene-co-maleic anhydride）NPs（PDVBMAH NPs）through a self-stable precipitation polymerization process.The size and morphology of these PDVBMAH NPs were characterized in detail by scanning electronic microscopy,and their chemical structure was determined by IR.The results showed that these NPs were highly cross-linked and their diameter was about 30 nm with narrow distribution.Additionally,the DVB and MAH endow the NPs with reactive surface anhydride and pendant vinyl groups,and these particles could be further functionalized through reaction of these groups.A plausible pathway was proposed for the formation of PDVBMAH NPs.