Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Powder Diffraction”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 703 records · Page 39Linked to original sources
PubMed1990

Interaction of adenylic acid with alkaline earth metal ions in the crystalline solid and aqueous solution. Evidence for the sugar C'2-endo/anti, C'3-endo/anti and C'4-exon/anti conformational changes.

The reaction of adenosine 5'-monophosphoric acid (H2-AMP) with the alkaline earth metal ions has been investigated in aqueous solution at neutral pH. The solid salts of Mg-AMP.5H2O, Ca-AMP.6H2O, Sr-AMP.7H2O and Ba-AMP.7H2O were isolated and characterized by Fourier transform infrared, 1H-NMR spectroscopy and X-ray powder diffraction measurements. Spectroscopic and other evidence showed that the Sr-AMP.7H2O and Ba-AMP.7H2O are isomorphous, whereas the Mg-AMP.5H2O and Ca-AMP.6H2O are not similar. The Mg2+ binding is through the N-7 (inner-sphere) and the phosphate group (outer-sphere via H2O), while the Ca2+ binds to the phosphate group (inner-sphere) and to the base N-7 site (outer-sphere through H2O). The Sr2+ and Ba2+ bind to H2O molecules, H-bonding to the N-7, N-1 and the phosphate group (outer-sphere). In aqueous solution, an equilibrium between the inner- and outer-sphere metal ion bindings can be established. The sugar moiety exhibited C'2-endo/anti conformation, in the free H2-AMP acid and the magnesium salt, C'3-endo/anti in the calcium salt and unusual C'4-exo/anti, in the strontium and barium salts.

Adenosine Monophosphate↗
PubMed1986

Sugar adducts with alkaline earth metal ions. Interaction of L-arabinose with Sr(II) and Ba(II) ions and the effects of metal ion binding on the sugar anomeric configurations.

The reaction between L-arabinose and hydrated Sr(II) or Ba(II) halide salts has been studied in H2O solution and adducts of the type M(L-arabinose)X(2).4H(2)O, where M = Sr(II) or Ba(II) and X = Cl- or Br- have been isolated and characterized by means of Fourier transform infrared spectroscopy, 1H-NMR spectroscopy, molar conductivity and X-ray powder diffraction measurements. Due to the marked spectral similarities with those of the structurally known Ca(L-arabinose)X2 . 4H2O (X= Cl- or Br-) compounds, the Sr(II) and the BA(II) ions are eight-coordinated, binding to two l-arabinose molecules via O1, O5 of the first and O3, O4 of the second sugar moiety and to four H2O molecules. 1H-NMR spectroscopy indicated that the free L-arabinose has the beta-anomer configuration in aqueous solution, whereas the alpha-anomer isomer is preferred by Mg(II), Ca(II), Sr(II) and Ba(II) ions, on complexation.

Journal Article↗
PubMed1987

Sugar interaction with biologically active cis-PtCl2(NH3)2 (anticancer) and its inactive trans isomer.

The interaction of D-glucuronic and D-gluconic acids with cis- and trans-PtCl2(NH3)2 (cisplatin and transplatin) has been investigated in aqueous solution and solid complexes of the type cis-[PtL(NH3)2]L.H2O and trans-[PtL2(NH3)2]L.H2O, where L = D-glucuronate or D-gluconate anions, are isolated and characterized by means of Fourier transform-infrared and 1H-NMR spectroscopy, and molar conductivity and X-ray powder diffraction measurements. Spectroscopic and other evidence indicated that the sugar anions bind monodentately in trans-[PtL2(NH3)2].H2O and bidentately in cis-[PtL(NH3)2]L.H2O complexes through the carboxylate oxygen atoms and other sugar donor groups. The strong sugar intermolecular hydrogen-bonding network is altered to that of the sugar-OH...NH3(H2O)...OH-sugar, upon platinum-ammine interaction. The D-glucuronate anion has the beta-anomer configuration both in the free salt and in these platinum-sugar complexes.

Cisplatin↗
PubMed1986

Physical characterization of solid forms of urapidil.

Polymorphic forms of urapidil were prepared by various techniques. Three polymorphic forms were identified and their solid-state properties were characterized by thermal behaviour, X-ray powder diffraction, IR spectra, intrinsic dissolution rates, solution calorimetry and scanning electron microscopy. Solution calorimetry was used to determine each polymorph in mixtures of Forms I and II, with a reproducibility of +/-3%. The stability of the three polymorphic forms was followed over a period of three months under different conditions and it was concluded that Forms I, II and III of urapidil were enantiotropic.

Journal Article↗
PubMed1990

Physico-chemical characterization of a new salt of ibuprofen.

A new salt of ibuprofen was prepared by reaction with t-butylamine; its formation was confirmed by IR and 1H-NMR spectroscopy. The salt was characterized by thermoanalytical, X-ray powder diffraction and solubility studies. The salt was found to be 1.5 times more soluble in water than was ibuprofen, with an enthalpy of solution of -8.84 kcal mol-1.

Butylamines↗
PubMed1992

Thermal behaviour and binary phase diagram of (S)-(+)-4,4'-(1-methyl-1,2-ethandiyl)-bis-(2,6-piperazinedione) (dexrazoxane), a cardioprotective agent, and of its (R)-(-)-enantiomer.

The binary phase diagram of (S)-(+)-4,4'-(1-methyl-1,2-ethandiyl)-bis-(2,6-piperazinedione), 1 (dexrazoxane), a cardioprotective agent, and of its (R)-(-)-enantiomer, 2, has been investigated by differential scanning calorimetry (DSC); the equimolecular mixture of 1 and 2 corresponds to a racemic compound (racemate) whose melting point is higher than that of the enantiomers. Thermal behaviour (DSC) is examined and discussed in comparison with the data obtained by other physical methods (IR spectroscopy and X-ray powder diffraction).

Algorithms↗
PubMed1994

A spectroscopic investigation of DuP 747 polymorphs.

DuP 747, a selective kappa agonist analgesic, was found to have at least two polymorphic forms, and this was confirmed by X-ray powder diffraction. DSC and thermomicroscopic studies indicated the polymorphic pair to be monotropic. Solubility studies suggested the relative stability of the two forms to be similar. The infrared (IR) and Raman spectra of the two crystal forms were significantly different, and their complementary nature was shown from the differences in peak intensities. Solid-state 13C-NMR data of the polymorphs showed only minor differences between the two forms. When viewed on the molecular level through the use of vibrational and NMR spectroscopies, the conformation of the molecule in the two polymorphs appears to be roughly equivalent. The magnitude of the spectral differences of the two polymorphs is, however, consistent with those that can be expected for two crystal forms that have resulted from different modes of packing, as caused by the solvent environment.

Analgesics↗
PubMed1994

Crystallinity, hygroscopicity and dissolution of moricizine hydrochloride hemihydrate.

A typical anhydrous moricizine hydrochloride, an antiarrhythmic agent, is a non-hygroscopic crystalline material. Three lots of moricizine hydrochloride were found to deliquesce within a day at 85% relative humidity, exhibit different X-ray powder diffraction (XRPD) patterns and have more rapid dissolution rate than that of typical anhydrous material. No change in XRPD pattern was observed when the solvent (ethanol) was removed from these lots by heating to 80 degrees C. A two-step water release was observed by thermogravimetric analysis (TGA): a surface water release and a water of hydration release, for these heated samples. The stoichiometry of the water of hydration suggests that it is a hemihydrate. The dissolution rate of the hemihydrate was faster than that of typical anhydrous material. This hemihydrate could be converted to a typical anhydrous material by heating to 90 degrees C. The granules obtained by a simulated wet granulation process on typical lots and typical lots containing up to 20% of hemihydrate exhibited similar physical behaviour to that of typical anhydrous material.

Calorimetry, Differential Scanning↗
PubMed2006

Low-magnesium uranium-calcite with high degree of crystallinity and gigantic luminescence emission.

Cabrera (Madrid) low-Mg calcites exhibit: (i) an unusual twofold elevation in X-ray diffraction pattern intensity; (ii) a 60-fold elevation of luminescence emission, compared to six common natural calcites selected for comparison purposes; (iii) a natural relatively high radiation level of circa 200 nSvh(-1) not detected in 1300 other calcites from the Natural History Museum of Madrid. Calcites were analysed by the X-ray diffraction powder method (XRD), cathodo-luminescence spectroscopy in scanning electron microscopy (CL-SEM), thermoluminescence (TL), differential thermal analysis (DTA), X-ray fluorescence spectrometry (XRF) and particle size distribution (PSD). The Cabrera calcite study shows: (i) helicoidally distributed steps along the (0001) orientation; (ii) protuberance defects onto the (0001) surface, observed by SEM; (iii) XRF chemical contents of 0.03% MgO, 0.013% of Y(2)O(3), and 0.022% of U(3)O(8), with accessory amounts of rare earth elements (REE); (iv) DTA dissociation temperature of 879 degrees C; (v) TL maxima peaks at 233 and 297 degrees C whose areas are 60 times compared to other calcites; (vi) spectra CL-SEM bands at 2.0 and 3.4 eV in the classic structure of Mn(2+) activators; (vii) a twofold XRD pattern explained given that sample is a low-Mg calcite. The huge TL and CL emissions of the Cabrera calcite sample must be linked with the uranyl group presence. This intense XRD pattern in low-Mg calcites could bring into being analytical errors.

Calcium Carbonate↗
PubMed2005

Rietveld refinements and spectroscopic studies of the structure of Ca-deficient apatite.

Nine samples of Ca-deficient apatite (Ca-def Ap) were prepared from suspensions of CaHPO4 (monetite) at 90 degrees C by raising the pH from approximately 4 through release of NH3 produced by the hydrolysis of urea. Products were dried at 100 degrees C for 24h and studied by chemical analyses, X-ray powder diffraction (XRPD) (and Rietveld analysis of this data), Ca/P ratio determination (quantitative phase analysis of samples after heating to 900 degrees C from Rietveld analysis of XRPD data), scanning electron microscopy, He pycknometry, 1H and 31P MAS NMR spectrometry and Fourier transform infrared and Raman spectroscopy. All samples contained apatite, but three also contained monetite. Infrared and Raman spectroscopy confirmed the presence of HPO4(2-) and absence of carbonate ions in the six monetite-free samples. Mean results for the six samples were: a = 9.4320(40), c = 6.8751(31) A; unit cell formula from chemical analysis neglecting protonation of phosphate ion, Ca(9.303(50))(PO4)6(OH)(0.606(99)).1.97(12)H2O; theoretical density 3.10 g cm(-3); experimental density (mean for three samples) 3.15 g cm(-3); and Ca/P mole ratio from chemical analysis and phase analysis after heating to 900 degrees C, 1.550(8) and 1.550(2), respectively. An earlier assignment of a line at 6 ppm in the 1H NMR spectrum of similar samples to HPO4(2-) ions could not be confirmed; hence no information about the HPO4(2-) ion content could be derived, in disagreement with the previous NMR study. A shoulder at approximately 0.9 ppm relative to 85 wt% H3PO4 in the 31P NMR spectrum was assigned to HPO4(2-) ions. Occupancies from the Rietveld structure refinements indicated preferential loss of Ca from Ca2 sites compared with Ca1, but the loss was substantially smaller than expected from chemical analyses. It is suggested that imperfect modelling of the structure in the refinement, particularly disorder associated with the Ca2 site, resulted in errors in Ca2 occupancies. The P-O bonds were slightly shorter than those in stoichiometric hydroxyapatite, rather than longer as might be expected from protonation of phosphate tetrahedra. However, consideration of known acid phosphate structures indicated that it was unlikely that the increase in P-O lengths would be sufficient to be detected. The observed decrease was tentatively assigned to the presence of Ca2+ ion vacancies.

Algorithms↗
PubMed2005

Synthesis and drug release behavior of poly (trimethylene carbonate)-poly (ethylene glycol)-poly (trimethylene carbonate) nanoparticles.

ABA-type triblock copolymers poly (trimethylene carbonate)-poly (ethylene glycol)-poly (trimethylene carbonate) were synthesized by ring-opening polymerization of trimethylene carbonate initiated by dihydroxyl poly (ethylene glycol). The critical micelle concentration of amphiphilic triblock copolymers in aqueous solution was determined by fluorescence spectroscopy using 9-chloromethyl anthracene as fluorescence probe. Core-shell-type nanoparticles were prepared by the dialysis technique. Transmission electron microscopy images showed that these nanoparticles were regularly spherical in shape. Micelle size determined by dynamic light scattering is 50-160 nm. Anticancer drug methotrexate (MTX) as model drug was loaded in the polymeric nanoparticles. X-ray powder diffraction spectra showed that model drugs were molecularly dispersed in the core. In vitro release behavior of MTX was investigated.

Antineoplastic Agents↗
PubMed2005

Influence of magnesium doping on the phase transformation temperature of beta-TCP ceramics examined by Rietveld refinement.

The influence of Mg doping in Ca(3)(PO(4))(2) on the transformation temperature of beta-tricalcium phosphate (beta-TCP) to alpha-tricalcium phosphate (alpha-TCP) was examined. A maximum substitution by 14 mol% of Mg(2+) on Ca(2+) sites in the beta-TCP structure was determined for powders calcinated at 1025+/-10 degrees C. X-ray powder diffraction analysis (XRPD) in combination with Rietveld method (TOPAS 2.1) was employed for quantitative phase analysis and structural refinement. The synthesized and characterized Mg-doped samples were sintered in air atmosphere in a vertical tube furnace at suitable temperatures ranging from 1460 to 1680 degrees C and subsequently quenched to room temperature, in order to stabilize alpha-TCP. The beta to alpha transformation temperatures were determined by differential temperature analysis and XRPD analysis.

Biocompatible Materials↗
PubMed2004

Melting behaviour of D-sucrose, D-glucose and D-fructose.

The melting behaviour of d-sucrose, d-glucose and d-fructose was studied. The melting peaks were determined with DSC and the start of decomposition was studied with TG at different rates of heating. In addition, melting points were determined with a melting point apparatus. The samples were identified as d-sucrose, alpha-d-glucopyranose and beta-d-fructopyranose by powder diffraction measurements. There were differences in melting between the different samples of the same sugar and the rate of heating had a remarkable effect on the melting behaviour. For example, T(o), DeltaH(f) and T(i) (initial temperature of decomposition) at a 1 degrees Cmin(-1) rate of heating were 184.5 degrees C, 126.6Jg(-1) and 171.3 degrees C for d-sucrose, 146.5 degrees C, 185.4Jg(-1) and 152.0 degrees C for d-glucose and 112.7 degrees C, 154.1Jg(-1) and 113.9 degrees C for d-fructose. The same parameters at 10 degrees Cmin(-1) rate of heating were 188.9 degrees C, 134.4Jg(-1) and 189.2 degrees C for d-sucrose, 155.2 degrees C, 194.3Jg(-1) and 170.3 degrees C for d-glucose and 125.7 degrees C, 176.7Jg(-1) and 136.8 degrees C d-fructose. At slow rates of heating, there were substantial differences between the different samples of the same sugar. The melting point determination is a sensitive method for the characterization of crystal quality but it cannot be used alone for the identification of sugar samples in all cases. Therefore, the melting point method should be validated for different sugars.

Calorimetry, Differential Scanning↗
PubMed2005

The sorption of hydrogen sulfide from hot syngas by metal oxides over supports.

Six 5 wt.% metal sorbents including Mn, Fe, Cu, Co, Ce and Zn supported on gamma-Al2O3, prepared by the incipient wetness impregnation method with calcination at 700 degrees C for 2 h, have been investigated for sorption of hydrogen sulfide in the temperature range of 500-700 degrees C. The sorption experiments were conducted in a fixed-bed reactor in terms of breakthrough curves and characterized by X-ray powder diffraction. The results reveal that the copper and manganese sorbents exhibit the best performance because they provide nearly 100% utilization, but the copper sorbent has a lower sulfur sorption capacity compared with the manganese sorbent. The zinc and cerium sorbents are not good candidates attributed to the vaporization of zinc and unexpected product for cerium. Effects of support materials on 5 wt.% manganese were also investigated by using gamma-Al2O3, SiO2 and TiO2 in this study. Five weight percent Mn/gamma-Al2O3 shows the best performance among support candidates. On the basis of XRPD and BET surface area analysis, TiO2 appears a huge loss in BET surface area associated with a significant formation of rutile form.

Adsorption↗
PubMed2005

Contrasting lead speciation in forest and tilled soils heavily polluted by lead metallurgy.

The concentration trends and chemical fractionation of Pb was studied in eight tilled and forest soil profiles heavily polluted by Pb metallurgy in the Pribram district, Czech Republic. The highest Pb concentrations were observed in surface and subsurface horizons attaining 35,300 mg kg-1 in forest soils and 1233 mg kg-1 in tilled soils. Total Pb concentrations were one order of magnitude lower in tilled soil due to intensive ploughing and annual crop off-take. The results of the Tessier sequential extraction procedure showed the preferential binding of Pb in forest soils to operationally-defined exchangeable positions and soil organic matter (oxidisable fraction). The Pb exchangeable fraction is thought to correspond to weak electrostatic binding on the functional groups of organic matter. In tilled soil, Pb is predominantly bound to operationally-defined Fe and Mn oxides (reducible fraction). A comparison with the background Pb concentration values showed a strong contamination even in mineral horizons IIC and confirmed a strong vertical mobility of Pb within the soil profiles. The calculated mobility factors (MF) showed that up to 72% of Pb is mobile and bioavailable in forest soils. In contrast, the bioavailability of Pb in tilled soils was significantly lower as the MF accounted for up to 30%. In the most polluted horizon of forest soil profile, the X-ray powder diffraction (XRPD) analysis confirmed the presence of anglesite (PbSO4), derived likely from the smelter emissions.

Agriculture↗
PubMed2006

Gamma radiation-induced grafting of a cationic monomer onto chitosan as a flocculant.

Grafting of (2-methacryloyloxyethyl) trimethyl ammonium chloride onto chitosan through gamma-radiation in acidic aqueous solutions was achieved for production of a novel flocculant. The grafted copolymer was characterized by Fourier-transform infrared, X-ray powder diffraction and thermogravimetric analysis. The effects of reaction parameters, such as total absorbed dose, dose rate, monomer concentration and temperature, on grafting percentage were investigated. The flocculation capacities of the grafted copolymer were evaluated with 0.25% (w/v) kaolin suspensions using the standard jar test. The results demonstrate the superiority of the grafted copolymer over chitosan as a flocculant.

Cations↗
PubMed2004

Phase behaviour of transkarbam 12.

Transkarbam 12 (T12), the carbamic acid salt of omega-aminocaproic acid dodecyl ester, is a recently synthesized substance, whose high permeation enhancing activity through the human skin was found for certain drugs. In this work, the thermotropic phase behaviour of T12 has been studied by means of various techniques, namely, DSC, FTIR and FT-Raman spectroscopy, X-ray powder diffraction, and DRS. The temperature development of the X-ray reflections as well as of the conformationally sensitive Raman bands and the IR bands have been observed. At room temperature, the hydrocarbon chains of T12 exhibit a highly ordered structure, arranged in an orthorhombic perpendicular subcell. On heating, two transitions occur at 54 and at 66 degrees C. The first transition is related to the disruption of the carbamate structure and changes in the polar head group. The other transition represents the melting of hydrocarbon chains and the subsequent release of carbon dioxide. The time required for the rebinding of carbon dioxide and the reformation of the carbamate structure is dependent upon numerous factors and it was not possible to precisely determine the length of this process.

Aminocaproates↗
PubMed2005

Adsorption on hydrophobized surfaces: clusters and self-organization.

The arrangement of liquid molecules on surfaces bristling with alkyl chains is deduced from adsorption studies, X-ray powder diffraction data, and microcalorimetric measurements of swelling-type layered materials, especially clay minerals. Small polar molecules such as water, ethanol, formamide, dimethylsulfoxide, and aromatic compounds are clustered between the alkyl chains pointing away from the surface. The energetic contribution related to the movement of the alkyl chains from direct contact with the surface atoms into upright positions is decisive. The importance of the interactions between the liquid molecules on the structure of the adsorption layer is clearly indicated by the changes of the adsorption layer thickness by salt addition. Thermodynamic data are obtained from surface excess adsorption isotherms from binary liquid mixtures combined with microcalorimetric measurements. Long-chain adsorptives such as long-chain alcohols interact with the surface alkyl chains by forming stable bimolecular films. These films undergo a series of higher-order phase transitions into kink- and gauche-block structures as the consequence of rotational isomerization of the alkyl chains. Such transitions are considered elementary processes in self-assembling films (layer-by-layer deposition, fuzzy films, Langmuir-Blodgett technique), and lipid membranes.

Adsorption↗