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تحضير ودراسة المركبات SnxBa4Ca2Cux+4Oy وYnBa5Cun+5Oy == Preparation and Characterization of the SnxBa4Ca2Cux+4Oy and YnBa5Cun+5Oy Compounds

اسم المؤلف: رؤى فخري هادي
اسم المشرف: عماد خضير الشكرجي
الموضوع العام: علوم الفيزياء
السنة: 2015
الموضوع الدقيق: الفيزياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The present study includes the preparation of SnxBa4Ca2Cux+4Oy and YnBa5Cun+5Oy compounds with (x = 3, 4, 5, 6, 7) and (n=3, 5, 7) by solid state reaction (SSR) method. The study was to conclude the superconductor behavior of both compounds. The prepared samples were analyzed by Meissner effect primary, and the excess oxygen content was measured by using Iodomertric titration method. The samples characterized by XRD patterns with computer program that was used to determine the value of lattice constant, Scanning Electron Microscope (SEM), Energy dispersive X - ray spectroscopy (EDS) to study the grain morphology and also resistivity measurement was performed by Van der Pauw method to conclude the nature of behavior.The resistivity measurement results of Sn - Ba - Ca - Cu - O system showed that the semiconducting behavior, increases with decreasing the temperature toward low temperature, the lowest and the highest normal resistivity were found at x=6 and at x=4, respectively. The system Y - Ba - Cu - O showed a superconductor behavior with high transition temperature, the Tc at n=3 of about (113.6 K), the sample prepared with n=5 has Tc=113 K, meanwhile the sample prepared with n=7 has Tc=105 K.The x - ray analyses for SnxBa4Ca2Cux+4Oy samples showed that the tetragonal structure, and the c - parameter increased by increasing the value of (x) until reach to maximum value at x=5 then return back decreasing at x=6 and 7. The x - ray diffraction analysis of the compound YnBa5Cun+5Oy has orthorhombic phase and when Y - atom concentration and the number of CuO2 layer increased tend to increase b and c - axis.The Scanning Electron Microscopy (SEM) results showed that the appearance of nanostructure in Sn6Ba4Ca2Cu10O22 and Sn7Ba4Ca2Cu11O24 samples in the range (100 - 300 nm), whereas the other samples of Sn - familywas a microstructure. On the other hand, the Y - 358 had large grains randomly comparable with Y - 5 5 10, Y - 7 5 12 addition to absent the interfaces distances from Y - 358. The results of EDS showed that the agreement of the peaks appeared with the theoretical values.

دراسة عليه ونظريه لفعالية بعض العقاقير كمثبطات لتاكل الالمنيوم معدن وبعض سبائكه في المحلول المحلي == Experimental and Computational Studies of Some Drugs as Corrosion Inhibitors for Aluminium and Some Its Alloys in Saline solution

اسم المؤلف: سمر ثامر حميد
اسم المشرف: شذى فاضل نارين السعيدي | تغريد علي سلمان
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: This thesis involves the investigation of the corrosion behaviour of pure aluminium as well as of two of aluminium - base alloys (5052Al and 2024Al) in sodium chloride solution over a temperature range (283 - 323 K) with and without ampicillin (AMP.), cephalexin (CEX.) and amoxicillin (AMOX.) as inhibitors.The results of electrochemical experimental study revealed that : 1. The current density increases with increasing temperature in the range of (283 - 323) K.2. The inhibition efficiency increases with increasing the concentration of inhibitors (AMP., CEX., and AMOX.), this means that these inhibitors act as an adsorption inhibitors on the surface for the corrosion of pure Al, 5052 Al, and 2024 Al in 3.5% NaCl.3. The inhibition efficiency of AMP., CEX., and AMOX. decreases with increasing temperature from 283 to 323 K. 4. According to the corrosion potential, AMP., CEX., and AMOX. act as mixed type inhibitors since corrosion potential does not change approximately in NaCl solution.5. The thermodynamic parameters of corrosion ΔH, ΔG, and ΔS have been calculated at different inhibitors concentrations and temperatures. The values of ΔG and ΔH indicate the spontaneous and exothermic corrosion processes respectivelly.6. The general behaviour for the kinetic studies depend on the Arrhenius equation. Kinetic data show that the adsorption of AMP., CEX., and AMOX. on the surface of in 3.5% NaCl is physisorption type.7. The negative values of thermodynamic functions of adsorption, ΔGads and ΔHads obtained from Langmuir isotherm, indicate the spontaneous and exothermic adsorption processes respectively.This thesis also includes theoretical calculation of ampicillin, cephalexin and amoxicillin molecules using the density functional theory (DFT) (B3LYP) with 6 - 31G basis set, which indicate that AMOX. is best inhibitor.The comparison of theoretical and experimental data exhibit good relation.The surface study by using Scanning Electron Microscopy (SEM) has been accomplished and the images show a smoother surface for pure aluminium sample in the presence (7.5×10 - 4 M) of ampicillin due to the formation of a protective barrier film through adsorption process.

تحضير اقطاب بوليمرية جديدة للسلفاميثوكسازول واستخدامها في تحديد بعض الادوية == Preparation of new polymeric electrodes for sulfamethoxazole and their use in determining some drugs

اسم المؤلف: سراء عبد العزيز ابراهيم
اسم المشرف: خالدة حميد محمد السعيدي
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: In this study two types of ion - selective electrodes (ISEs) were prepared based on PVC matrix membrane.First, four ion - selective electrodes for sulfamethoxazole (SMZ) which based on sulfamethoxazole (SMZ) and tungestophosphoric acid (TPA) ion - paircomplexas the electro - active materials were prepared. Second, six ion - selective electrodes for sulfamethoxazole (SMZ) whichbased on sulfamethoxazole (SMZ) and sodium tetraphenylborate (NaTPB) ion - paircomplex as the electro - active materials were also prepared.In both types of ISEs, some of the selectedplasticizers were used such as; Di - octyl phthalate (DOPh), Tri - butyl phthalate (TBPH), Tri - butyl phosphate (TBP),Nitrobenzene (NB), Acetophenone (AP) and o - Nitrophenyloctylether (o - NPhOE) in PVC matrix.The electrodes parameters, linear range of concentration,Nernestian slope, limit of detection, response time, life time, working pHrang and selectivity were evaluated. Also the statistical treatments wereapplied for the results that include : relative standard deviation (RSD),relative error (Re.), and confidence limit for concentration. The results showed : The first type ISEs were : SMZ - TPA+DOPH (E1),SMZ - TPA+TBP (E2),SMZ - TPB+AP (E3) andSMZ - TPA+NB (E4), give the linear Range from (1×10 - 5 - 1×10 - 2, 1×10 - 7 - 1×10 - 2, 1×10 - 5 - 1×10 - 2 and 1×10 - 5 - 1×10 - 2 M), and the slopes are (52.008, 58.381, 56.909 and 50.309 mV/decade)respectively, with detection limits are (9×10 - 6, 9×10 - 8, 6×10 - 6 and 7×10 - 6M), response time of 10 - 3 M (30, 28, 36 and 25 second) and the lifetimewere about (29, 27, 20 and 9 days) respectively.The second type, were : SMZ - NaTPB+TBPH (L1), SMZ - NaTPB +NB (L2), SMZ - NaTPB +TBP (L3), SMZ - NaTPB +AP (L4),SMZ - NaTPB +DOPH (L5) and SMZ - NaTPB +o - NPhOE (L6) give the linear range from (1×10 - 5 - 1×10 - 2, 1×10 - 5 - 1×10 - 2, 1×10 - 5 - 1×10 - 2, 1×10 - 5 - 1×10 - 2, 1×10 - 5 - 1×10 - 2 and 1×10 - 5 - 1×10 - 2M), the slopes are (53.609, 49.608, 56.810, 55.709, 50.808 and 51.808 mV/decade)respectively, with detection limits of (9×10 - 6, 8.5×10 - 6, 8×10 - 6,8.9×10 - 6, 7.5×10 - 6 and 7×10 - 6M), response time of 10 - 3 M (16, 14, 24, 19, 16 and 20 second) and the lifetime were about (12, 6, 24, 17, 26 and 7 days) respectively.The best electrode from first kind is (E2) and from the second kind is (L3), both were used to determine the sulfamethoxazole in pure samples. The working pH for (E2) electrode was ranged from (1.6 - 6.8) and the working pH for (L3) electrode was ranged from (1.7 - 6.9). The interferences measurements in the presence of (Na+, K+, Cu+2, Mn+2, Fe+3, Al+3, trimethoprim, starch, sucrose and gelatin ) were studied for both electrodes using the separated method and mixed method for selectivity coefficient determination.The ISE (E2) gave a good electrochemical characterizationamong the others and it has been used successfully for the determination ofsulfamethoxazole in the Pharmaceutical Samplesusing different potentiometricmethods.Also UV - spectrophotometric method was used which include the normal spectra,forsulfamethoxazole solutions (0.990x10 - 4, 0.996x10 - 4,0.999x10 - 4, 1.004x10 - 4, 1.005x10 - 4)M in wavelengthequal 259.00 nm. The analytical methods results showed to be simple, rapid and with a good accuracy by comparing between normalspectra and direct method of Ion selective electrode by using F - test.The results shown, that the sulfamethoxazole canbe determined by using Ion selective electrode method because the value of the (F) experimental less than the value of the (F) theoretical at 95% confidence limit. Since F - calculated less than F - table, we concluded that there is no difference in precision between two methods.

تحري الخواص الحرارية لبعض السوائل الايونية الحاوية على اليوريا والاستمايد == Investigation of Thermal Properties for some Ionic Liquids containing Urea and Acetamide

اسم المؤلف: هدى سلام عبد
اسم المشرف: هادي محمد علي عبود
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Characterization of some room temperature ionic liquids (RTILs) as candidates for thermal storage media and heat transfer fluids in thermal applications were investigated. Five ionic liquids prepared from ammonium alum [NH4Al(SO4)2.12H2O] pronounced S, as inorganic salt with urea [NH2CONH2] pronounced U, or acetamide [CH3CONH2] pronounced A, as organic compounds, and aluminum nitrate [Al(NO3)3.9H2O] pronounced N with urea or acetamide compounds in different mole ratios were investigated alone and with addition of some improving materials to study their synergetic effect using thermo - gravimetric analysis (TGA), Differential Scanning Calorimetery (DSC), X - ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy and conductivity measurements. Thermo - physical properties such as enthalpy ΔH, heat capacity Cp and thermal energy storage capacity were determined. It was found that hydrated aluminum nitrate : acetamide (1 : 22 mole ratio, AN2IL) alone and hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) alone or with addition of some materials characterized with high density, chemical stability, heat capacity, thermal energy storage capacity and wide temperature range. The results indicated that ionic liquids alone or with addition of some materials could be considered as a promising candidate for liquid thermal storage media and heat transfer fluids.Studying the synergetic effect by addition of some alkali metal hydroxide (NaOH) with hydrated aluminum nitrate : urea (1 : 1.2 mole ratio, UNIL) and KOH with hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) ionic liquids increased thermal energy storage capacity of these ionic liquids, while the addition of NaOH to hydrated aluminum nitrate : acetamide (1 : 22mole ratio, AN2IL) gave less thermal stability and storage capacity of ionic liquid.Also addition of alkaline earth metal oxide MgO, CaO to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) and BaO to hydrated aluminum nitrate : urea (1 : 1.2 mole ratio, UNIL) decreased thermal stability, heat capacity and thermal energy storage capacity than ionic liquid alone.Moreover, addition of transition metal oxide (VOSO4.5H2O, CuO and ZnO) to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) increased thermal stability and storage capacity of hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL), while the addition of NiO to hydrated ammonium aluminum sulfate : urea (1 : 5 mole ratio, USIL) only improve thermal stability of ionic liquid

التثبيت الضوئي لمتعدد كلوريد الفانيل باستخدام معقدات مخلبية == Photostabilization of poly(vinyl chloride) by chelate complexes

اسم المؤلف: علي نجاح حسن
اسم المشرف: عماد عبد الحسين يوسف السراج
الموضوع العام: علوم الكيمياء
السنة: 2015
الموضوع الدقيق: الكيمياء
الدرجة: ماجستير
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Five metal complexes of Cu(II), Cd(II), Zn(II), Ni(II) and Sn(II) with {4 - (Benzylidene - amino) - 5 - pyridin - 4 - yl - 4H - [1,2,4]triazole - 3 - thiol}, of Schiff base ligand (L), were prepared in alcoholic medium.The ligand (L) and its metal complexes were characterized qualitatively by using : FTIR, UV - visible spectroscopy, magnetic susceptibility, conductivity measurements and 1H NMR only for ligand. The ligand acted as bidentate which coordinated to the metal ions through sulphur and nitrogen of Azomethine group.According to the spectral data of the complexes a tetrahedral geometry was suggested for these complexes, except Cu(II) complex which exhibited octahedral geometry distorted to square planar structure.The metal complexes were used to enhance the photostabilization of PVC contains a concentration of ML2 0.5 % by weight. The photostabilization of PVC films were studied at room temperature under irradiation of light with λ=313 nmand an intensity of 7.75 X 10 - 7 einstein dm - 3 sec - 1.The photostabilization activity of these compounds was determined bymonitoring the carbonyl (ICO), polyene (Ipo) and hydroxyl (IOH) indices and weightloss method with irradiation time. It was found that the (ICO), (Ipo) and (IOH)indices values increased with irradiation time and this increase found to depends on the type of additives.The surface morphology for these films was studied during irradiation time.The changes in viscosity average molecular weight of PVC with irradiation time were also tracked (using THF as a solvent). The quantum yield of the chain scission (Φcs) of these complexes in PVC films was also evaluated.The following trend was obtained for the photostabilization effect on PVC films in presence of additives as shown below : CuL2 , CdL2 , ZnL2 , SnL2 , NiL2 Increasing the photostability According to the obtained experimental results, mechanisms were suggested, depending on the structure of the complexes.