Geochemical characterization the waters of Foggaras the Continental Intercalary Aquifer of Timinoune region (south west Algeria)

The study of the Continental Intercalary (C.I) groundwater of the region of Timimoune (southwestern Algeria), based on physico-chemical data (major elements), allowed to understand the geochemistry of foggaras water. The aquifer is contained in the formations of the Lower Cretaceous (Albian and Barremian). The waters are strongly mineralized with an average value 2g / l.The waters have a clear predominance of facies chlorinated-sodium. The risk is high to excessive soil salinization, and the risk of medium alkalinity to very high. Statistical analysis led us to reach two conclusions, the first is that, variable electrical conductivity (EC), dry residue (RS), Na+, Ca2+, Cl-, SO4 --, mineralization, are best correlated and responsible the signing of the mineral load of water, the second is that the nitrate ion (NO3-) opposite to the above-mentioned variables mark its anthropogenic origin. Keywords: Continental Intercalary, mineralization, salinity, PCA, Nitrat

Sterol composition of caper (Capparis spinosa) seeds

Caper is a perennial shrub of the Mediterranean Basin. The most important economical species is Capparis spinosa. Sterols of C. spinosa seed oil isolated from seven Tunisian stands were identified andquantified. C. spinosa contained  high levels of phytosterols (2240.4 mg/kg of total extracted lipids), of which -sitosterol, with 1390 mg/kg, was the most abundant (57.53%). Campesterol and stigmasterol accounted for 382 and 265 mg/kg, respectively (17.05 and 11.85% of the total sterols, respectively). C. spinosa seed oil also contained a high level of 5-avenasterol (6%). We detect also brassicasterol (3.39 mg/kg). Cholesterol and campestanol are detected in much lower levels. These results bring attention to the richness of C.spinosa seed oil with sterols which are the most important class of the minor components

Removal of methylene blue with a highly effective hydroxyapatite-silica nanocomposite

Two Hydroxyapatite-silica nanocomposite adsorbent (HApS220 and HApS230) were successfully synthesized using sol-gel technique. The samples were characterized by powder X-ray diffraction (XRD), Infrared spectroscopy (IR), scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS), which confirmed the formation of a Hydroxyapatite-silica nanocomposite. The synthesized powders were then used for adsorption of methylene blue (MB). Both compounds possessed high absorption capacities, the adsorption equilibrium time is around 10 min. HApS230 sample shows higher adsorption capacity compared to HApS220. Furthermore, isotherm studies show that the adsorption used is an ion exchange process and that Temkin isotherm describes the adsorption better compared to the Langmuir and Freundlich and Dubinin-Radushkevich isotherms. Kinetics studies confirm that the adsorption follow the pseudo-second order model and chemisorption mechanism. Thermodynamics’ studies confirm that the adsorption of MB on HApS samples is a spontaneous endothermic process. The average removal effectiveness of MB reached about 89.02% (6.389 mg/g adsorption capacity) and 91.36% (6.55 mg/g adsorption capacity) for HApS220 and HApS230 respectivel

Physicochemical study of magnesium zinc codoped-hydroxyapatite

Mg-Zn-doped hydroxyapatites in the system Ca9.4-xMg0.6Znx(PO4)6(OH)2 (x= 0, 0.1, 0.2, 0.4 and 0.6) were synthesized via sol-gel method. The obtained powder was calcined at 600°C and 700°C. X-ray diffraction (XRD) patterns and Infra-Red (IR) spectra confirmed the formation of pure hydroxyapatite up to 2% Zn content (a trace of β-pyrophosphate is detected for x=0), while a mixture of hydroxyapatite and β-TCP was formed for 4 mol%. With 6 mol%, only β-TCP formed. Moreover, at 700°C, all powders turned to be composed of solely β-TCP. The unit cell constants have also been calculated and match well with hexagonal (P63/m) hydroxyapatite

PROPRIETES STRUCTURALES DE COPOLYMERES BISEQUENCE ET TRISEQUENCE LINEAIRES ET DE LEUR HOMOLOGUE CYCLIQUE EN SOLUTION DILUEE STRUCTURAL PROPERTIES OF LINEAR DIBLOCK AND TRIBLOCK COPOLYMERS AND THEIR CYCLIC HOMOLOGOUS IN DILUTE SOLUTION

SUMMARYThe structural properties of linear block copolymers in solution aroused a considerable interest and are the subject of manytheoretical and experimental investigations. However, their cyclic counterparts received only a limited attention fromresearchers mainly because of difficulties related to their synthesis with high-molecular weights and a low polydispersity. Thisstudy was justified by the relatively recent light scattering measurements carried out by Amis et al. on a cyclic diblockcopolymer and its linear triblock counterpart made up of polystyrene (PS) and poly(dimethylsiloxane) (PDMS). In this work,the adopted theoretical approach is based on the random phase approximation when the polymeric systems under study areplaced in similar conditions of temperature, concentration, composition and mass than those covered experimentally by Amisand others. The main objective of this study is intended to present a theoretical formalism allowing a systematic analysis of thescattering data, relating to block copolymers of arbitrary architectures, and to suggest some indications relating to theirtreatment. In terms of thermodynamic and structural properties, the results obtained reveal differences between the two typesof copolymers. In particular, contrary to what was brought back by Amis and his collaborators, the discrepancies, shownbetween the radii of gyration of linear block copolymers and their cyclic counterpart, being sufficiently large, it should bepossible to highlight them in experiments by light scattering.RESUMELes propriétés structurales de copolymères séquencés linéaires en solution ont suscité un intérêt considérable et fait l'objet denombreuses investigations théoriques et expérimentales. Cependant, leurs homologues cycliques n'ont retenu l'attention qued'un nombre limité de chercheurs principalement du fait de difficultés liées à leur synthèse avec des poids moléculaires élevéset une faible polydispersité. Cette étude a été motivée par des mesures de diffusion de lumière relativement récentes réaliséespar Amis et al. sur un copolymère biséquencé cyclique et son homologue triséquencé linéaire constitué de polystyrène (PS) etde poly(diméthylsiloxane) (PDMS). Dans ce travail, l'approche théorique adoptée est basée sur l'approximation de la phasealéatoire en plaçant les systèmes polymériques considérés dans des conditions de température, de concentration, decomposition et de masse similaires à celles couvertes expérimentalement par Amis et autres. L’objectif premier de la présenteétude consiste à présenter un formalisme théorique permettant une analyse systématique de données de diffusion, relatives àdes copolymères séquencés d'architectures arbitraires, et de suggérer quelques indications concernant le traitement de celles-ci.En termes de propriétés thermodynamiques et structurales, les résultats obtenus révèlent des écarts entre les deux types decopolymères. En particulier, contrairement à ce qui a été rapporté par Amis et ses collaborateurs, les différences, relevées entreles rayons de giration de copolymères séquencés linéaires et de leur homologue cyclique, étant suffisamment importantes, ildevrait être possible de les mettre en évidence expérimentalement par diffusion de lumière

Learning of chemistry of solution with help of computer simulation

Le présent article rend compte d'une expérimentation utilisant des simulations informatiques de titrages acide-base dans des situations didactiques d'apprentissage basées sur l'investigation et la participation de l'apprenant dans la construction de son savoir. Deux approches dans l'utilisation des simulations de titrages pH-métriques à l'aide du logiciel «SIMULTI2» sont mises en place et évaluées avec un groupe d'enseignants en formation continue et un groupe d'élèves-professeurs en formation initiale. On montre que les simulations informatiques créent un contexte pédagogique favorisant l'apprentissage par la découverte ou l'exploration basée sur les conflits cognitifs

ON THE STATIC AND DYNAMIC SCATTERING FROM LINEAR AND BRANCHED POLYELECTROLYTES AT VARIOUS SCREENING LENGTHS PROPRIETES DE DIFFUSION STATIQUE ET DYNAMIQUE DE POLYELECTROLYTES LINEAIRES ET RAMIFIES A DIVERSES LONGUEURS D’ECRAN

During the two last decades, branched polyelectrolytes have been thoroughly studied from theoretical and experimentalstandpoints. In this report, we attempt to compare the behaviour of highly branched polyelectrolytes to that of their linearcounterparts at low ionic strength. As expected, the expansion behaviour of the branched materials is considerably less than ofthat of the corresponding linear chains. Surprisingly, in the former case (sphere-like behavior), the ratio of the radius ofgyration to the hydrodynamic radius ρ=Rg/Rh shows an opposite behaviour as compared to the second one (rod-like behavior);indeed, contrary to the case of linear chains for which this ratio increases, that of branched homologous decreases as the ionicstrength is lowered. Analyzis of the data, depicted in Kratky plots, reveals substantial discrepancies between the bothpolymeric structures. Moreover, at high ionic strength, one observes a rod-like structure that undergoes a transition to adisordered conformation which is not however that of a random coil, whereas, at low one, it appears that the two double- helixunfold and the loop strongly expands. Ces deux dernières décennies, les polyélectrolytes ramifiés ont été activement étudiés sur le double plan théorique etexpérimental; le propos de cette étude est de tenter de comparer le comportement de polyélectrolytes fortement ramifiés à celuide leurs homologues linéaires pour des forces ioniques faibles. Comme attendu, l'expansion des matériaux ramifiés estconsidérablement moindre que celle des chaînes linéaires correspondantes. Cependant, il est surprenant que, dans le premiercas (comportement d’une sphère), le rapport du rayon de giration au rayon hydrodynamique ρ =Rg/Rh montre uncomportement opposé à celui correspondant au second cas (comportement de bâtonnet); en effet, contrairement au cas deschaînes linéaires pour lesquelles ce rapport croît, celui de leurs homologues ramifiés diminue à mesure que la concentrationionique est abaissée. L’analyse des données, mises en évidence dans la représentation de Kratky, indique des écartssubstantiels entre les deux structures polymériques. Par ailleurs, pour une force ionique élevée, on observe une structure enforme de bâtonnet qui subit une transition vers une conformation désordonnée qui n'est cependant pas celle d’une pelotestatistique, tandis que, pour des forces ioniques basses, il apparaît que les deux double-hélices ne se replient pas et la boucles’étend fortement

Camel breeding development project in Tunisia

Camel breeding is of great socio-economic importance in southern Tunisia. Although, the size of the national camel herd has decreased over the years from 120000 to 56000 heads in 2014. Illegal export, low breeding efficiency, social modernization and lack of investment are the major causes of this decline. To remedy this situation, the Tunisian government has established a national program for development and research on camel production. This program is based on grants to farmers to encourage rearing of replacement females and fattening camels; improvement of pastures and water infrastructure, promotion of applied research in specialized centers. Research eff orts are centered on health, nutrition and improvement of rangelands, development of reproductive biotechnologies and genetic improvement. An attempt was carried out to genotype the local breeds of camels. Development of semen preservation and artificial insemination has met several challenges inherent to the peculiarities of reproduction in this species