Growth and Characterization of Holmium Oxalate Heptahydrate Crystals

Single crystals of holmium oxalate heptahydrate are grown by gel diffusion method using organic agar gel as a medium of growth. The crystals grow in the agar gel with hexagonal morphology having well defined habit faces Powder X-ray diffraction results show that the crystals belong to monoclinic system bearing the space group P21/c with cell parameters;a = 12.197? , b = 11.714 , c = 6.479 , α = 90°, β = 120.12°, γ = 90°, V = 799.6? 3. Fourier transform Infrared spectrum of the crystals shows the presence of water and other associated functional groups. Thermogravimetric analysis support the presence of 7 H2O molecules associated with holmium oxalate crystal lattice. The thermal decomposition in the nitrogen atmosphere leads to the formation of holmium oxide as the final product.

Preparation of microsized silver crystals with different morphologies by a wet-chemical method

A wet-chemical method was presented for preparation of spherical, flowerlike, hexagonal, and triangular microsized silver crystals. Well-defined particles were prepared by mixing of iron（II） sulfate heptahydrate solution with silver nitrate solution at the presence of different modifiers with high-speed stirring at 8-20℃. It is found that the diameters of resulting products are 0.6-6.0 um and the morphologies of the silver microcrystals are greatly affected by the introduced modifiers. It is concluded that the microsized silver crystals with different morphologies can be synthesized by introducing appropriate modifiers at appropriate experimental parameters. Scanning electron microscopy and X-ray diffraction were used to characterize the resulting products.

Preparation of micro-sized and uniform spherical Ag powders by novel wet-chemical method

A novel wet-chemical method was presented for the preparation of the micro-sized and uniform spherical Ag powders on a mass-production scale.The well-defined particles were synthesized by mixing the iron(II) sulfate heptahydrate solution with silver nitrate solution directly by high-speed stirring at room temperature.It is found that a large number of micro-sized and uniform spherical particles with rough surfaces are obtained.The mass ratio of iron(II) sulfate heptahydrate to silver nitrate greatly affects the shape of particles,and when it is relatively low,spherical particles cannot be obtained.The reaction temperature has a great impact on the particle size.As the reaction temperature increases from 8 to 15°C,the mean diameter of particles decreases from 3.5 to 1.6 μm.The additive n-methyl-2-pyrrolidone improves the surface smoothness and compactness of the particles while the particle size is kept unchanged.Scanning electron microscopy,X-ray diffractometry and energy dispersive X-ray analysis were used to characterize the particle products.

Quality of Drugs Based on Ferrous Sulfate Dispensed in a Basic Health and Commercial Pharmacy in a City in the Amazon Region

Background: For the WHO, anemia is a serious public health problem, with an emphasis on deprivation anemia, which has socioeconomic conditions as determining factors for its development. Among nutritional anemias, the most relevant is iron deficiency, whose main form of prevention and treatment is supplementation with ferrous sulfate dispensed in the public health system, with the need to periodically check whether the drug has the quality required by regulatory health agencies. Thus, the objective of this study was to analyze the quality of the ferrous sulfate medication, from the same laboratory, and dispensed in a basic health unit (BHU) and a commercial pharmacy (CF). Materials and Methods: An analytical, qualitative and quantitative study of ferrous sulfate heptahydrate (25 mg/mL in 100 mL syrup), carried out on 20 BHU and 10 from CF, both from the same laboratory, but in different batches. Samples were subjected to organoleptic analysis and verification of iron content, pH, volume and density. Data were compared with values recommended by the Brazilian pharmacopoeia 5th edition. Results: Three batches were evaluated: 4659 of from the CF;4574 from the BHU1, and 4576 from the BHU2, stored in accordance with RDC 304/19 of ANVISA. All showed compliance with some organoleptic characteristics;and stable values in pH (3.61 - CF;3.67 - BHU1;3.65 - BHU2), density (1.079 - CF;1.088 - BHU1;1.086 - BHU2) and individual volume (not less than 95% of the declared value). However, it was not possible to detect the odor of herbs;the average volume of batch BHU1 was below the declared value, and the iron content of both BHUs was above the maximum value of pharmacopoeia standards. Conclusion: Samples did not show full compliance with the physical and chemical parameters evaluated, suggesting deviation in the quality of the medication.

CoCl_2·6H_2O or LaCl_3·7H_2O Catalyzed Biginelli Reaction. One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1 H)-ones

An efficient synthesis of 3,4-dihydropyrimidinones from aldehyde, β-ketoester and urea in ethanol using cobalt chloride hexahydrate or lanthanum chloride heptahydrate as acatalyst was described. Compared to the classical Biginelli reaction, this new method consistentlyhas the advantage of good yields (56%―99%) as well as short reaction tune (4―5 h).