First pages:

تحضير وتشخيص معقدات بعض العناصر الانتقالية مع ليكاندات نتروجينية ودراسة فعاليتها الحيوية == Preparation And Identification Complexes of Some Transition Metales With Nitrogeneus Ligands And Study Its Biological Activity

Author name: علي ابراهيم علي بكر الجبوري

Supervisor name: نهلة عبد الحميد عبد الجبار

General topic: Chemistry

Specific topic: Chemistry

Degree: Master

University: Tikrit University - College Of Science - Chemistry Department

Language: Arabic

University location: Salahaddin

First pages:

Abstract: تضمن البحث تحضير كاشفين جديدين هما الكاشف 3 - ((4,5 - diphenyl imidazole) diazenyl) benzene sulfonic acid ويرمز له (DPIDBSA) والكاشـــف2 - ((3 - methoxy phenyl) diazenyl) - 4,5 - diphenyl imidazole ويرمز له (MBDPI) وذلــــك من مفاعلة ملـح الديازونيـوم ل | This thesis included the preparation of the two new reagents 3 - ((4,5 - diphenyl imidazole) diazenyl) benzene sulfonic acid (DPIDBSA) and 2 - ((3 - methoxy phenyl) diazenyl) - 4,5 - diphenyl imidazole (MBDPI) by reacting adiazonium salt solution of (3 - aminobenzene sulfonic acid) and (3 - methoxyaniline) with (4,5 - diphenyl imidazole) in alkaline ethanoic Solution.The identity of these reagents have been characterized by spectral methods such as(UV - Vis) , FTIR , another physical properties (m.p.) and elemental analysis.The ionization constant of the reagent (DPIDBSA) was determine using spectroscopic method , the pKa was equal to 9.9.Six chelating complexes of the above reagents were synthesized with metal ions) Co2+, Ni2+, Cu2+). The two wavelength of maximum absorption for the two reagents were found (422nm) and (416nm) respectively in ethanol and for the complexes formed between these ions with these reagents were found at (476, 492, 504nm) and (455, 458, 496nm) for cobalt(II) , nickel(II) and copper(II) respectively in aqueous medium.It has been prepared after fixing the optimum condition of concentration and acidity function, through the study of UV - Vis spectrum for reacting of metal solution and two reagents solution. For wide range of pH (5 - 11) and concentration which obey to Beer - Lambert Law.The structures were determine according to the mole ratio method and continuous variation method which is obtained from the spectroscopic studies of the complex solutions. The ratios of (metal : reagent) are equal to (1 : 2) for all the complexes ions.The stability of complexes in the solutions was also studied at the optimum conditions.Diagnosis the solid prepared complexes by UV - Vis spectrum in ethanol solution showed high chromic shift from as compared with free reagents in visible region to all the complexes prepared.Micro elemental analysis for all the complexes were prepared and the percentage of Co(II) and Cu(II) were determined , using flame atomic absorption spectroscopy, it was noticed a great accord between theoretical and particle ratio.The infrared spectrum of chelating complexes also studied and it's compared with the two reagents spectrum. They give notice change with free two reagents spectrum. These showed new bands that were not found original in two reagents spectra but other bands have been changed in shape, in trinity and location. This may indicate that a coordination between the metal ions and the two reagents prepared.The Conductivity measurements for solutions at (1×10 - 3M) in ethanol solution have shown non - ionic character for all chelate complexes.From the above observations, it's suggested stereo shapes for complexes, that show the two reagents (DPIDBSA) and (MBDPI) behave as bidentit reagent, we can conclude that the proposed geometrical structure of all chelate complexes are octahedral.The study also included using spectrum method for determination stability constant of complexes in the thermal rang (25 - 45C?) for complexes with reagent (DPIDBSA) while the thermal rang was (10 - 30 C?) for complexes with reagent (MBDPI), and calculating ?G , ?H and ?S for complexes.The bacterial activity of the ligand and it's complexes were studied toward two type of bacteria : 1 - Pseudomonas. aurginosa 2 - StaphylloCoccus. aureusThe complex of Ni(II) with reagent (DPIDBSA) and the complexes of Co(II), Ni(II) and Cu(II) with reagent (MBDPI) and metal ions solution showed high bacterial activity on Pseudomonas. aurginosa while the solution of two reagents and all chelate complexes prepared also the aqueous solution of metal ions don't showed any activity toward the two type of bacteria (StaphylloCoccus. aureus) (G+ve).

Author name: نادية باقر حسين

Supervisor name: حسن عباس حبيب

General topic: Chemistry

Specific topic: Chemistry

Degree: Master

University: University of Al-Qadisiyah - Faculty Of Education - Chemistry Department

Language: Arabic

University location: Qadisiyah

First pages:

تقدير بعض الملوثات العضوية وازالتها من محاليلها المائية باستخدام اطيان عراقية واطيان عراقية محورة وتطبيق برنامج شبه تجريبي لدراسة الامتزاز نظريا == Determination And Removal of Some Organic Pollutants From Aqueous Solution By Using Iraqi Clays, Modified Clays And Applied Semi - Empirical Program To Theoretical Adsorption Study

Author name: اقبال سلمان محمد

Supervisor name: سعدية احمد ظاهر | خلود عبد صالح

General topic: Chemistry

Specific topic: Chemistry

Degree: Master

University: University of Baghdad

Language: English

University location: Baghdad

First pages:

Abstract: تم في هذه الدراسة تحضير معقدات مخلبية للموليبدنيوم (V) مع ليكاندات ثنائي الالكيل ثنائي ثايوكاربامات وتشخيصها طيفيا" باستخدام مطيافية الاشعة المرئية والفوق البنفسجية ومطيافية الاشعة تحت الحمراء, وهذه المعقدات هي : 1 - فنيل هايدرازايدو - ثلاثي (ثنائي مثيل ث | This study included Preparation of chelate molybdenum(V) complexes with diethyldithiocarbat ligands and characterized them by (UV - Visible) and infrared (FTIR) spectroscopy.These complexes are : 1 - Phenyl hydrazido - tris - dimethyldithiocarbato molybdenum(V) [Mo(N2ph)(S2CNMe2)3].2 - Phenyl hydrazido - tris - diethyldithiocarbato molybdenum(V) [Mo(N2ph)(S2CNEt2)3].3 - (2,4 - dinitro - Phenyl hydrazido) - tris (diMethyldithiocarbamato molybdenum(V). [ Mo( N2ph - (NO2 )2) (S2CNMe2)3 ]. 4 - (2,4 - dinitro - Phenyl hydrazido) - tris (diethyldithiocarbamato molybdenum(V). [ Mo( N2ph - (NO2 )2) (S2CNEt2)3 ].The study of the kinetics of chemical decomposition for these chelates complexes by using irradiation of these complexes solution, by using a mono wave light (? = 365nm) and temperature (25?C) for (60 min) in ethanol solvent. The result for all complexes were that the order of photochemical decomposition was first order reaction. As well as the rate constants of photo decomposition reactions (kd) were calculated by observed a spectral changes during irradiation process. To know the best conditions for decomposition of these complexes, it is necessary to study the effect of several factors on photo chemical behavior for complexes which included : Effect of concentration of complexes, where five concentrations of complexes have been studied and found that the highest decomposition rate have observed at lowest concentration (2.5x10 - 5M). In addition, study the impact of change in intensity of light on decomposition rate. The result was when the light intensity increase, rate of complexes decomposition also increased. Also study a decomposition of complexs at temperature range (25 - 40?C). The result was when increasing temperature, the rate of complexs decomposition was increas, also the values of activated energy of all complexes where calculated and the results where show in the table : Activated Energy (kj / mole) Complex24.808 B122.971 C120.209 B217.778 C2 Also study effect of pH value at ranging (3 - 11) and found that the rate of the complexes decomposition increased when pH of solutions decreases. The effect of four alcoholic solvent were studied such as (methanol, ethanol, 1 - butanol and isopropanol), and found that the highest decomposition rate of these complexes achieved in Methanol, while the lowest decomposition rate of these complexes achieved in Isopropanol. In addition study the effect of each of nitrogen gas, oxygen gas and the atmospheric air on the rate of complexes decomposition and compile the results with recorded results in normal conditions, the highest decomposition rate observed in presence of oxygen gas and the lowest decomposition in presence of nitrogen gas. The mechanism of photo chemical decomposition of these complexes has been interpreted by spectrophotometric technique, were the conclusion that have been obtained that there is (redox - reaction) happening in these complexes and the output of processes of homo cleavage of bond (M - L) that leading to reduction of metal ions and oxygenation of ligand and formation free radicals.

هرمون الانتي مولرين كدالة لمتلازمة تكيس المبايض في امصال النساء العراقيات == Serum Anti - Mullerian Hormone As A Marker of Polycystic Ovary Syndrome In Iraqi Women

Author name: شهد فوزي عبيد عبد الواحد الخفاجي

Supervisor name: بشرى فارس حسن | غريد خليل محمد علي

General topic: Chemistry

Specific topic: Chemistry

Degree: Master

University: University of Baghdad - College Of Science For Girls

Language: Arabic

University location: Baghdad

First pages:

Abstract: يتضمن البحث تنقية المحاليل المائية المخففة من الملوثات العضوية صبغة الرودامين وصبغة الكونغو الاحمر بطريقتين الطريقة الاولى كانت امتزاز هذه الصبغات على سطح البتونايت ضمن Al2O3، ZnO،TiO 005 ( جزء بالمليون استعلمت المركبات الثانوية 2 - مدى من التراكيز ) 05 ) | The present work deals with the purification of diluted aqueous solutions from organic pollutants Rhodamine B (RhB) and Congo red (CR) dyes with two methods. The first one was adsorption these dyes on bentonite in range (50 - 250)mgl - 1, Nanocompounds,TiO2, ZnO, Al2O3 and quaternary ammonium salts Hexadecyl tri methyl ammonium bromide (HDMAB), long chain hydrocarbon compounds Sodium dodecyl sulfate(SDS) in different amounts (0.01 - 0.1)g/10g of bentonite were used to modify the adsorption capacity to remove the RhB and CR dyes from aqueous solutions. Both bentonite and modified bentonite are firstly characterized using SEM, AFM and FTIR techniques.The effect of dyes concentration, contact time, effect of initial dye concentration and contact time, adsorbent dosage, and amount of modifiers on the percentage removal have been studied. The modified bentonite with SDS. TiO2 , ZnO increased the percentage removal(R%) of RhB dye from 80% by natural bentonite to 99.3%,98.9% and98.7% respectively, the other dye CR modified bentonite with HDMAB,TiO2 ,ZnO, increased the R% from 81.3% to 99.6%, 99.0% and 98.8%,while adding Al2O3 did not success to increase the R% of RhB and CR on bentonite surface The study exhibits that Langmuir and Freundlich models gave geed fitted to the experimental adsorption at 25°C.The second method deals with advanced oxidation process by using photo - Fenton catalyst(Fe2+,H2O2 and UV light) to degradates of two dyes RhB and CR, the effect of Fe2+ concentration,H2O2 concentration , initial dye concentration and effect of pH at different interval time have been studied.results indicated that simultaneous utilization of UV irradiation with Fentons reagent increase the degradation degree of RhB and CR dyes quickly lose their color, indicating that the dissolves organics have been oxidized, the maximum color removal were obtained at pH 2.0,250 mgl - 1of Fe2+,300 mgl - 1of H2O2for RhB at 240 minute while for CR maximum removal were at pH 3.0,200 mgl - 1of Fe+2,350 mgl - 1of H2O2 at 270 minute.The photo - Fenton degradation process was monitored by HPLC chromatogram of RhB and CR dye solutions. The intensity of the peaks are gradually decreased with irradiation time.The irradiation time after three hours show no HPLC peaks detected, the results are in a good agreement with the results obtained from the UV visible spectrum.In this study semi - empirical methods are used to calculate the molecular orbital energies. This calculation let to suggest the best surface active material which can be used to modify the adsorption efficiency for RhB and CR on Iraqi bentonite surface. The theoretical study results are compared to experimental results achieved in experimental studies on some organic pollutants and modified bentonite by SDS and HDMAB. Using SDS led to the best adsorption efficiency for RhB while HDMAB lead to best efficiency for CR dye. The enthalpy of formation, dipole moment and energy of molecular orbital HOMO and LUMO energies levels were calculated for the two dyes and the two modifiers.

التقدير بتقنية الحقن الجرياني المستمر التعكرية لايون الاوكسونيوم من خلال مبادل ايواني واستعمال مصفوفة خطية للتشعيع بنظام فوتومتري 5SX1 - T - 1D وباستعمال خلية شمسية كمتحسس == Turbidimetric - Cfia Determination of Oxonium Ion Through Ion Exchange Resin With The Use of Linear Array Ayah 5Sx1 - T - 1D Solar Microphotometer

Author name: احمد ازهر منصور الصراف

Supervisor name: عصام محمد علي شاكر الهاشمي

General topic: Chemistry

Specific topic: Biochemistry

Degree: Master

University: University of Baghdad - College Of Science For Girls

Language: English

University location: Baghdad

First pages:

Abstract: لوحظ في الفترة الاخيرة ظهور مرض متلازمة تكيس المبايض في الاناث خلال سن الانجاب، ان نشوء المرض ربما يعود للاختلال الهرمونات ( المبايض، الغدة النخامية ) ومقاومة الانسولين. ومؤخرا تم استخدام هرمون الانتي - مولرين كمؤشر في التشخيص الدقيق لمرض متلازمة تكيس | In the recent period there had been increased emergence of polycystic ovary syndrome in females during the reproductive age, which may be due to hormonal imbalances (ovaries, pituitary gland) and insulin resistance. Recently Anti - Mullerian hormone had been used as an indicator for determining the degree and accurate diagnosis of polycystic ovary syndrome in serum of patients as well as the measurement fasting insulin and other hormones routine.Aim of study : - ? Proof that anti - mullerian hormone is a marker for diagnosis of polycystic ovary syndrome patients. ? Compares hormones level as : anti mullerian hormone, fasting insulin, luteinizing hormone, follicle stimulation hormone, Prolactin, testosterone between polycystic ovary syndrome and normo - ovulatory women. ? Correlate the level of anti mullerian hormone with other the biochemical features as hormones follicle stimulation hormone, luteinizing hormone, testosterone, prolactin and insulin resistance.? To find a cut - off value for anti - mullerian hormone in Iraqi women with polycystic ovary syndrome. Subjects and Methods : - Forty patients with polycystic ovary syndrome , aged ( 20 - 35) years attending AL - Seweraa hospital / Waset , Kamal AL - Samarai hospital / Baghdad for infertility and gynecology and Al Elwiya Maternity Teaching Hospital were included in the present study , also forty normal fertile females ,aged (21 - 37) years who serve as control group. Blood samples were taken from all subjects from day 2 - 5 day of menstrual cycle. The level of all parameters were quantitatively determined in patients and control subjects by Vidas. Except Anti - mullerian hormone and insulin hormone quantitatively determined in patients and control subjects by Enzyme - Linked Immuno Assay [ELISA]. Test using commercially available Kits as well as the important measurements that had been done include body mass Index.Results : - ? There was a significant [P = 0.0001] increase in Anti mullerian hormone in polycystic ovary syndrome patients compared to controls.? There was a significant [P = 0.0001] increase in luteinizing hormone in polycystic ovary syndrome patients compared to controls , while the level of follicle stimulation hormone and fasting serum glucose was found to be insignificantly when compared with control group.? There was a significant [P = 0.001] increases in testosterone and prolactin hormones in polycystic ovary syndrome patients compared to controls.? Anti - mullerian hormone is more sensitive and specific than the other tests in predicting the occurrence of the disease with a cut off value (>7.9). ? The mean serum level of fasting insulin, homeostatic model assessment was significantly [P=0.0001] elevated in the polycystic ovary syndrome patients when compared to that found in the control group.

تحضير وتشخيص بعض المشتقات الجديدة للبنزايميدازول المعوضة == Synthesis And Characterization of Some New Substituted Benzimidazole Derivatives

Author name: سحر ثامر عداي

Supervisor name: عبد الامير مطلك فنجان

General topic: Chemistry

Specific topic: Analytical Chemistry

Degree: Master

University: University of Baghdad - College Of Science - Chemistry Department

Language: English

University location: Baghdad

First pages:

Abstract: The project conducted in this research work was carried out from December 2013 to June 2014 which leads to this thesis, which are in five chapters. All these chapters cover up the survey, the practical part of preparing, manufacturing and using Atomic force Microscopy that have been adopted during this research work, and the results were subjected into various internationally used mathematical and data treatments.Chapter OneDiscusses the acids, ion exchange, precipitation reaction, crystal growth theories, light scattering, turbidity and describe FIA in general, it is classification and fundamentally involved ideas without forgetting the use and applications of FIA. Chapter one also discusses derivative spectroscopy, definition, classification, the applications. This chapter ends with the aim of the project.Chapter Two : In this chapter a complete description of the chemicals and ion exchange column, their preparations and their use throughout this project. This chapter describes the use of flow system with all it is components (i.e. peristaltic pump, connection tubes, junction(Y - junction), six ports injection valve, ion exchange column and measuring readout system). Chapter Three : Consists of four parts The first part describes the design of Ayah 5SX1 - T - 1D Solar cell CFIA and deals with calculation of dispersion to evaluate the change in concentration ateach location of the designed manifold system via the chasse of an air bubble. The second part deals with the analysis carried out in this research work. Determination of oxonium ion (HClO4, HNO3, H2SO4 and HCl) via turbidity of solution of zinc (II) ion in cation exchange column - K3[Fe(CN)6] system. A comprehensive detailed study was carried out using Ayah 5SX1 - T - 1D Solar cell CFIA microphotometer. The linear range (10 - 100 mMol.L - 1), limit of detection (43.20, 57.14, 30.28, 30.97 ng/sample) for above mentioned acids and percentage of relative standard deviation < 2% for five successive measurement of 20 and 80 mMol.L - 1 for used acids. The method was applied successfully for determination of the mentioned oxonium ion in pure and commercial samples. A comparison was made between the newly developed method and the classical method pH meter using of paired t - test. It was noticed that there was no significant difference between two methods.The third part deals with the analysis carried out in this research work. Determination of oxonium ion (HClO4, HNO3, H2SO4, HCl) via turbidity of solution of copper (II) ion in cation exchange column - K3[Fe(CN)6] system. A comprehensive detailed study was carried out using Ayah 5SX1 - T - 1D Solar cell CFIA microphotometer. The linear range (10 - 100) mMol.L - 1, limit of detection (42.94, 39.14, 20.61, 26.11 ng/sample) for above mentioned acids and percentage of relative standard deviation < 2.5% for five successive measurement of 20 and 100 mMol.L - 1 for used. The method was applied successfully for determination of the mentioned oxonium ion in pure and commercial samples. A comparison was made between the newly developed method and the classical method pH meter using paired t - test. It was noticed that there was no significant difference between two methods.The fourth part deals with the approache that was used through linear array Ayah 5SX1 - T - 1D continuous flow injection analyzer to distinguish between the responses that were obtained i.e. discrimination between the kind signals that were completely different.Chapter FourDeals with studying topography and morphography of the Zn3[Fe(CN)6]2 and Cu3[Fe(CN)6]2 complexes using atomic force microscopy. Chapter Five : This chapter concludes few interesting points based on the obtained results throughout this research work, such as conclusions and future work, Published work, and references. -

تقدير السبروفلوكساسين, النورفلوكساسين والحديد الثلاثي باستعمال الطرق الطيفية مع الاستخلاص بنقطة الغيمة == Determination of Ciprofloxacin, Norfloxacin And Iron (III) Using Spectroscopic Methods With Cloud Point Extraction

Author name: نورا سعد مبدر

Supervisor name: زهير عبد الامير خماس

General topic: Chemistry

Specific topic: Organic Chemistry

Degree: Master

University: University of Baghdad - College Of Science For Girls

Language: English

University location: Baghdad

First pages:

Abstract: يتضمن البحث تحضير ستة وثلاثون مشتق جديد من مشتقات]2 - (5 - كلورو - 1H - بنزو]د[ايميدازول - 2 - يل انيلين[، وقد تمت دراستها وتشخيصها بواسطة اجراء تحاليل اطياف الاشعه تحت الحمراء FT - IR)) واطياف الرنين النووي المغناطيسي للبروتونH - NMR)1) لها.تم تقسيم تح | This research includes synthesis of thirty six new derivatives of [2 - (5 - chloro - 1H - benzo[d]imidazol - 2 - yl)aniline] and these derivatives were characterized by their FT - IR and 1H - NMR spectra.The synthesized compounds were divided into three parts : - The first part involved : - 1 - Synthesis of 2 - (5 - chloro - 1H - benzo[d]imidazol - 2 - yl) aniline [1] by the reaction of 4 - chloro - 1,2 - diaminobenzene with anthranilic acid and hydrochloric acid as a reagent.2 - Acetylation of compound [1] by using acetic anhydride in order to obtaine the Acetamide compound [2]. 3 - Synthesis of N - [2 - (5 - chloro - 1H - benzo[d]imidazol - 2 - yl) phenyl) - hydroxyl N' - methyl] acetimidamide [3] by the reaction of compound [2]with hydroxyl amine hydrochloride and sodium carbonate.4 - Synthesis of Benzimidazolyl Chalcone derivatives [4 - 11] by the reaction of the compound [2] with various aromatic aldehydes such as benzaldehyde ,4 - nitro benzaldehyde,4 - chloro benzaldehyde and 4 - methyl benzaldehyde.The second part included : Mannich reaction was carried out based on the compound [1] using formaldehyde and different secondary amines such as piperdine , indole, diphenyl amine , morpholine , indole - 3 - acetic acid , and imidazole to offered [12 - 24]. The third part was synthesized as following : - 1 - Synthesis of Schiff bases [25 - 32] from the reaction of compound [1] with various aldehydes such as benzaldehyde, 4 - bromobenzaldehyde, 4 - hydroxy benzaldehyde, and glutar aldehyde.2 - Reaction of Schiff bases [26 - 29] with mercaptoacetic acid to give new compounds containing thiazolidin ring [33 - 36].

تحضير وتشخيص الدقائق النانوية لاوكسيد النحاسوز بواسطة الكتروليتات مختلفة == Preparation And Characterization of Cuprous Oxide Nanoparticles By Different Electrolytic Media

Author name: حيدر خضير خطار

Supervisor name: فؤاد عبد الامير السعدي | سامي وحيد راضي الحسناوي

General topic: Chemistry

Specific topic: Physical Chemistry

Degree: Master

University: University of Kufa - College Of Science For Girls - Chemistry Department

Language: English

University location: Najaf

First pages:

Abstract: في الواقع، لم تلقي عملية فصل واستخلاص الكميات الضئيلة من الادوية في العينات الحيوية وكذلك في المستحضرات الصيدلانية اهتماما واسعا وكبيرا باستعمال مايسمى الاستخلاص بنقطة الغيمة. وفي هذا الصدد، نعتقد ان العمل البحثي الحالي سوف يسهم في فتح افاق جديدة في تصم | The separation and extraction of trace amounts of medicaments in biological specimens, as well as in pharmaceutical formulations have not received much attention by using the so - called cloud - point extraction (CPE). In this context, we think that the present research work will contribute to opening new prospects in designing procedural steps and expands the applications of the cloud point extraction methodology in most important areas, including pharmaceutical sciences, forensic and environmental analyses. The present work concentrates on the developing of new eco - friendly procedures for determination of two selected antibiotic medicaments namely cirprofloxacin chloride (CIPRO) and norfloxacin (NOR) using iron (III) ion in human serums and pharmaceutical formulations, as well as the exploitation of these two drugs in chemical analysis as chelating agents for the detection of iron in pharmaceutical formulations via using cloud point extraction coupled with molecular spectrophometry. Generally, these methods implicate the use of a nonionic surfactant (Triton X - 114) as an extracting medium which entrap the hydrophobic colored complex formed between one of these drugs and iron (III) ion in acidic medium as a reaction system for designing the CPE procedures.This thesis includes three main chapters as follows;Chapter One summarizes some theoretical and practical principles of cloud point extraction (CPE) methods and then highlights the knowledge of the target analytes (CIPRO, NOR and iron) in term of their structures, pharmacological importance besides a concise chemical literature review for the estimation of these analytes by different analytical techniques. Chapter Two consists of an outline of instrumental techniques , general apparatus and chemicals used in the present work. The full analytical procedures for CPE which have been designed for the determination of the target analytes under study are made in this thesis.Chapter Three covers a detailed study for the discussion of the analytical data obtained throughout this work which can be summed up as follows;A. Formation of chelates between CIPRO or NOR and Fe(III) in acidic medium , where the drugs have individually been estimated in the resulting complex by spectrophotometry after the cloud point extraction at each respective ?max, and the use of developed method so that to determine any of the interested drug in human serum and pharmaceuticals. At first, the study was conducted to pinpoint the optimum conditions for the formation of complexes by CPE and the results were as follows; 1. The optimum experimental conditions for Fe - CIPRO and Fe - NOR complex for the determination of CIPRO and NOR respectively : H2SO4 concentration (5x10 - 4 M and 2.5x10 - 4M; Fe(III) concentration ( 6 ?g mL - 1 and 10 ?g mL - 1); Triton X - 114 amount ( 1%) for both drugs; temperature and time ( 75 °C at 25 min and 65 °C at 20 min).2. The achieved analytical figures of merit on applying the developed methods for CIPRO and NOR are : linear range (2.5 - 120 ?g mL - 1 ) for drugs, limit of detection (0.770 and 0.204 ?g mL - 1), Enrichment factor (143 and 280 fold), extraction efficiency (96.46 and 96.62%) and mean recovery percentage (98.89±0.87% and 98.95±1.09). 3. The newly established procedures have been applied for the determination of CIPRO and NOR in human blood serum and pharmaceuticals. For the determination of these medicaments in serum samples , the statistical paired t - test was used to test the significance of the proposed method comparing with the conventional UV - spectrophotometry, while in pharmaceuticals, the findings were compared statistically with quoted values that stated by the manufactures. B. Iron (III) ion was also determined in the pharmaceutical formulations based on the above reaction system in (A) via formation of yellow colored complexes with each medicament which extracted by micelles generated by CPE and subsequently detected spectrophotometrically at the same ?max of the above mentioned complexes. The optimum established conditions and the analytical data obtained could be summarized as follows : 1. The same optimum conditions were used in (A) except that the concentration of CIPRO or NOR here was of 7x10 - 5 M and Triton X - 114 amount of 0.6% in final solutions.2. The analytical figures of merit obtained on applying the developed methods for iron using CIPRO and NOR respectively; linear range (5 - 150 ng mL - 1); limit of detection (2.67 and 3.42 ng mL - 1); preconcentration factor (71 and 83 fold); mean recovery percentage (99.78±0.53% and 98.77±2.29); extraction efficiency (99 and 98.7%). 3. The effect of some additives of the pharmaceutical formulations was also studied and the iron determined in three selected formulations collected from local drugstores. The results were compared statistically with quoted values and shown not to be significant at 95% confidence level.

دراسة التاكل والحماية من التاكل لسبائك من حديد الفولاذ في ماء البحر باستخدام دقائق اوكسيد الزركونيوم وكربيد السليكون واوكسيد الالمنيوم النانوية == Corrosion And Corrosion Protection Studies of Carbon Steel Alloy In Seawater Using; Zirconia, Silicon Carbide And Alumina Nanoparticles

Author name: حيدر عبد الكريم يوسف

Supervisor name: خلود عبد صالح السعدي

General topic: Chemistry

Specific topic: Physical Chemistry

Degree: Master

University: University of Baghdad - College Of Science - Chemistry Department

Language: English

University location: Baghdad

First pages:

Abstract: يعتبر اوكسيد النحاسوز واحدا من المواد ذات الاستخدامات العلمية المتعددة الاغراض وذات الاهمية الصناعية الكبيرة ,ومنها استخدامه كمتحسس للغازات وفي العوامل المساعدة وكذلك في انتاج الواح الطاقة الشمسية ويدخل وبصورة كبيرة كمحطم للصبغات العضوية في مجال الكيمياء | Cuprous oxide (Cu2O) has been extensively studied because of its potential use in several electronic applications, which include solar cells and gas sensors. This Thesis is devoted to the synthesis, characterization of nano - structured cuprous oxide by using a simple electrochemical cell with a potassium chloride solution as an electrolyte, the electro cell contains a two high purity copper electrodes as a sheet form in different areas at varying sizes the area of the cathode was twice of the area of anode , the two electrodes zone were separated using a fine diameter silica diaphragm,Within this broad scope , the Thesis focuses on : • Production of different shape nano - crystals (Cu2O) and investigation of the correlation between experimental parameters and resulting microstructure.• Production of highly purity nano - crystalline Cu2O powder, with the estimation it’s by the available investigation instruments.• Study the different parameters, current density, bath temperature, KCl concentration , types of additives , time of precipitation, and there’s effects on the shape ,quantity ,surface roughness, powder color, on the Cu2O powder. Models have been proposed for the nano - crystal formation validated by several techniques uses such as X - ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM), and Fourier Transform Infra - Red spectroscopy (FTIR). The produced nanocrystals show good crystallinity with Cu2O purity and Copper oxide semiconductor nanoparticles were prepared by electrochemistry using galvanostatic and potentiostatic approaches. The optimum deposition conditions ( electrolyte composition , medium pH , type of additives, electrodes area ,current density , temperature of the electrolyte and applied potential of the cell) , to prepare the Cu2O nano particles have been identified; in particular the conditions that allow getting this product by using KCl ,(PVA ,SDS ,and glycerin as emulsifying agent) have been well identified for the first time. The configuration of deposited Cu2O , purity and amounts. These values depend on the electro deposition conditions such as the pH of the solution, the deposition potential and temperature. Where the study results showed that there is direct effect of these factors, it has been observed that the sizes of the precipitate crystalline decreased with increasing current density and especially at high bath temperatures its ranged about 10 - 20 nm , in addition to the effect of the percentage of additives emulsifier agents the best results at poly vinyl alcohol.. The X - ray diffraction pattern and 2? values reflect that the high purity of the deposit where obtained, without any of the other undesirable products like CuO, CuCl2 and CuCl. Also the FTIR analysis was considered. the effect of additives of the type of emulsifier on the crystalline form of the deposit, the PVA produced of the Star (Branches) crystals shape, the addition of the SDS compound leads to the form of the cubic , and the glycerin product the binary pyramid crystals shape.. Finally the conditions effect on the surface roughness of the precipitated powder also discussed. Depending of the electro - deposition conditions, different surface morphologies with various preferential crystal orientations were obtained for the temperatures of the electro - deposition of 80 °C , pH = 8 - 9 , The influence of several deposition parameters of the Cu2O, such as applied potential, pH, the temperature of the bath , the chemical composition, grain size and orientation parameters of the sample was systematically studied using X - Ray Diffraction , Atomic Force Microscopy, Transmission Electron Microscopy ,Fourier Transmission Infra - Red, and scanning electron microscopy.

تحضير وتشخيص وتقييم انواع جديدة من البولي يورثان القابلة للتفكك الاحيائي ودراسة تطبيقاتها الحيوية في اطلاق الدواء == Preparation , Identification And Evaluation of New Types of Biodegradable Polyurethane And Study Their Application In Drug Delivery

Author name: صابرين فرحان جواد

Supervisor name: محمد علي مطر

General topic: Chemistry

Specific topic: Physical Chemistry

Degree: Master

University: University of Al-Qadisiyah - College Of Science - Chemistry Department

Language: English

University location: Qadisiyah

First pages:

Abstract: Corrosion and corrosion protection of carbon steel (C.S) alloy in seawater (3.5% NaCl) was achieved in this thesis. Three types of nanoparticles (NPs) were used to protect C.S the first silicon carbide (SiC), second alumina (Al2O3) and the third zirconium oxide (ZrO2) nanoparticles (NPs). Electrophoretic deposition (EPD) technique was applied to coating the C.S surface. Different polyacrylic acid (PAA) percentage (0.1 - 1)% were added to the suspension solution of coating by the three types of NPs, to improve the protection efficiency (PE%) for the coated C.S surfaces.The corrosion rate with respect to uncoated and coated C.S with the three above NPs were measured. Different corrosion parameters were obtained; corrosion current density (icorr), corrosion potential (Ecorr), cathodic and anodic Tafel slopes (bc,ba), protection efficiency (PE%), polarization resistance (Rp) and the surface porosity (P%). The effect of temperatures (298 - 328)K on the corrosion of uncoated and coated C.S by the three NPs in presence and absence of PAA were also investigated and therefore activation energy (Ea) and preexponential factor (A) were calculated. Thermodynamic parameters ?G, ?H and ?S for all corrosion processes were obtained. Coated C.S were analysed using atomic force microscopy (AFM) to detect the morphology of surface and the particles size of coat layers which range from 60 - 103 nm, which greater than thestarting particles.The corrosion current densities (icorr) were increased generally with increasing temperatures for all cases and icorr reduced after coated C.S by different NPs in absence and presence PAA, therefore icorr reduced from 168.88 ?A.cm - 2 to 19.45, 28.71 and 30.2 ?A.cm - 2 for C.S coated by SiC, ZrO2 and Al2O3 respectively at 298K.While the Ecorr shifted to more active potential after coated by different NPs excepting when C.S coated by SiC in presence of (0.25%) PAA in coating solution suspension where Ecorr shifted to noble direction. The protection efficiency (PE%) of all coated C.S in absence and presence of PAA showed noteworthy degree of enhancement and the PE% ranged between (85 to 99.65)% for SiC , (69 to 91)% for ZrO2 and (77 to 87.9)% for Al2O3. The surface porosity (P%) were increased with increasing temperatures for all cases. The activation energy (Ea) values for the corrosion of coated C.S by different NPs lead to higher values than Ea for uncoated C.S and the highest value was (71.936) kJ.mol - 1 obtained when C.S coated by SiC in presence of (0.25%) PAA. The free energy (?G) Values for the corrosion of coated C.S generally more negatively than uncoated and the values of enthalpy (?H) for the corrosion of coated C.S by ZrO2 and Al2O3 were less negatively than uncoated C.S while coated C.S by SiC lead to more negatively ?H values.

تحضير وتشخيص مركبات حلقية غيرمتجانسة ودراسة الفعالية الحيوية لها == Synthesis And Identification of Heterocyclic Compounds And Study Their Biological Activity

Author name: رنا نعمة عطية

Supervisor name: ماجد جاري محمد | نغم محمود الجمالي

General topic: Chemistry

Specific topic: Chemistry

Degree: Master

University: University of Kufa - Faculty Of Education - Chemistry Department

Language: English

University location: Najaf

First pages:

Abstract: تضمن هذا البحث تحضير سلسلة انواع جديدة من البولي يوريثين المتفكك احيائيا والحساس لــلدالة الحامضية والذي يحتوي على مشتقات البنزوكائين المتضمنة مجموعة الازو بالبلمرة التكاثفية لـ 1,6 - hexamethylene diisocyanate في درجة حرارة 80 م مع مونمرات الازو، كيميائ | In this work series of new types of biodegradable and pH - sensitive polyurethane containing azo derivatives of benzocaine were synthesized by the condensation polymerization of 1,6 - hexamethylene diisocyanate at 80 ?C with the azo monomers. The chemically controlled release methods have been applied in which the benzocaine (drug) with active group (NH2) linked up with the spacer group (dihydroxy monomers) by azo bond formation.The First stage : The monomers synthesized from the reaction of (cyclohexanone , 1 - naphthole, 2 - naphthole , 4 - bromophenol , 3 - chlorophenol , phenol , 4 - (2,4 - dihydroxyphenyl)but - 3 - en - 2 - one , 4 - (4 - hydroxyphenyl)but - 3 - en - 2 - one and p - hydroxy acetophenone ) with acetone in presence of HCl as catalyst under reflux condition. M1 M2 M3 M4 M5 M6 M7 M8 M9The Second stage : The azo monomers were synthesized from the reaction of monomers : (M1 ,M2 ,M3 ,M4 ,M5 ,M6 ,M7 ,M8 ,M9 ,hydroquinone ,pyragollal ) with Benzocaine in presence of HCl , NaNO2 and NaOH 10% by stirring for one hour in ice bath at (0 - 5 ?C). AZO1 AZO2 AZO3 AZO4 AZO5 AZO6 AZO7 AZO8 AZO9 AZO10 AZO11 Where (R) : is the above monomers which shown in first and second stage.The Third stage : polyurethane azo was synthesized from the reaction between the azo monomers (which are shows in second stage) with 1,6 - hexamethylene diisocyanate in oil bath by refluxing for 8 hours at 80 ?C in dry nitrogene.where : ( R ) are the monomers which shown in first and second stage.The U.V - Visible , FT - IR , H1NMR techniques were used to confirm the chemical structure of the synthesized Polyurethane azo.A calibration curve between absorbance and concentration was constructed to stock solution of pure drug. the concentration of Benzocaine release was calculated by extrapolation of the result on the calibration curve every 24 hrs. The detection limit for Benzocaine was minimum used 0.001 gm/mol wavelength at 293 nm. Benzocaine was loaded into the polymeric matrix during in situ polymerization. The drug release from the benzocaine loaded was studied in two different medias ( pH=7.8, pH=4 ) at the human temperature.The results was shown that degradation of polyurethane azo in phosphate buffer solution was dependant in the pH value. In pH7.8 the polyurethane azo was rapidly released over 45 hrs. Incubation of polyurethane azo with rate cecal content at 37 ?C gradually released of benzocaine and the percentage of drug released was follow sequence (57% ,82% , 84% , 73% , 73% , 78% , 80% , 82% , 79% , 75% , 86% ) in 45 hrs. In pH=4 polyurethane azo was released slower than basic condition over 45 hrs. at 37 C, and the percentage of drug release was follow sequence (49% , 76% , 72% , 49% , 68% , 60% , 66% , 77% , 70% , 66% , 60%).The release rate of Benzocaine increased with increasing pH (i.e. , 7.8?4).

Author name: هالة باهر حمادي

Supervisor name: شذى عبد الودود عبد الرحمن

General topic: Chemistry

Specific topic: Biochemistry

Degree: Master

University: University of Baghdad - College Of Science - Chemistry Department

Language: English

University location: Baghdad

First pages: