Publications

6.078 articles found

6031

CHARACTERISTICS OF A UHF DISCHARGE USED AS ATOMIC SOURCE FOR A MASER

GHEORGHIU, OC; GHEORGHE, VN

1975, INTERNATIONAL JOURNAL OF ELECTRONICS, 39, 335

DOI: 10.1080/00207217508920490

6032

CLUSTER COHERENT POTENTIAL APPROXIMATION IN PRESENCE OF OFF-DIAGONAL DISORDER

HERSCOVICI, C

1975, PHYSICA STATUS SOLIDI B-BASIC RESEARCH, 72, 694

DOI: 10.1002/pssb.2220720228

6033

SYNTHESIS AND ELECTRICAL BEHAVIOR OF GA2MG5 TYPE STRUCTURE COMPOUNDS

POPA, M; BRADEA, I; IVANCIU, O; NICULESCU, D; CRUCEANU, E

1975, MATERIALS RESEARCH BULLETIN, 10, 1353

DOI: 10.1016/0025-5408(75)90096-3

6034

DIFFUSION OF CONVERTING IONS

POPESCU, A; MUSA, G

1975, REVUE ROUMAINE DE PHYSIQUE, 20, 9

6035

PERTURBATION OF GIBBS SEMIGROUPS

ANGELESCU, N; NENCIU, G; BUNDARU, M

1975, COMMUNICATIONS IN MATHEMATICAL PHYSICS, 42, 30

DOI: 10.1007/BF01609431

6037

GRAIN-SIZE EFFECT ON FIGURE OF MERIT OF SINTERED SOLID-SOLUTIONS BASED ON BI2TE3

JAKLOVSZKY, J; IONESCU, R; NISTOR, N; CHICULITA, A

1975, PHYSICA STATUS SOLIDI A-APPLIED RESEARCH, 27, 332

DOI: 10.1002/pssa.2210270202

6038

Popa, A; Ilia, G; Pascariu, A; Iliescu, S; Plesu, N

13 0

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6039

Physico-chemical properties of two anhydrous azathioprine forms and their interaction with typical pharmaceutical excipients: highlighting new findings in drug formulation development

Barbatu, A; Lungan, MA; Toulbe, N; Smaranda, I; Daescu, M; Baibarac, M; Manta, CM

, DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY

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The physico-chemical properties of two anhydrous AZA forms and their interaction with typical pharmaceutical excipients were assessed by applying various methods (such as PXRD, HPLC, TG/DSC, IR, Raman, PL or UV-Vis) in order to highlight new directions for drug formulation. The stability assessment of AZA anhydrous forms I and II was performed in order to determine the risk of degradation of the active ingredient by accidental exposure to nonstandard conditions in the industrial environment, under different storage, transport or processing conditions. The benefits of form II include increased resistance to chemical degradation over a wide range of pH, but further control of storage and processing conditions is necessary to avoid polymorphic transformation into form I. The solubility assessment on the AZA solid forms in different environments that simulate the conditions of the gastrointestinal tract has the advantage of a significantly increased solubility of form II compared with the commercial form I due to the modification of the crystalline structure. In the case of capsules compared to AZA form I or II as powder, an improvement in their solubility was observed, promoted by the presence of one or more excipients in the formulation mixture.

6040

A green way for pyruvic acid synthesis from biomass-derived L-malic acid on tetrahedral versus octahedral cobalt sites/hematite

Mitran, G; Urda, A; Pavel, OD; Neatu, S; Florea, M; Neatu, F

, BIOMASS CONVERSION AND BIOREFINERY

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A series of cobalt-iron mixed oxides, CoxFe3-xO4 (x = 0; 0.05; 0.1; 0.15), were synthesized by coprecipitation and tested for oxidative decarboxylation of malic acid to pyruvic or malonic acid. The characterization of catalysts was performed by different techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFT) and Ultraviolet-visible spectroscopy (UV-Vis). Among studied catalysts, Co0.15Fe2.85O4 sample (denoted Co3Fe) showed the highest malic acid conversion in oxidative decarboxylation reaction as well as the highest pyruvic acid yield. This behavior can be due to the fact that this sample has the highest content of tetrahedral Co2+ that replaces Fe3+ from octahedral position that determine an increased number of defects that play a crucial role for the malic acid conversion.