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تصميم منظومتي حقن جرياني ومتعاقب جديدتين لتقدير ايونCu(II) البنفسجية-المرئية وبمطيافية فوق EDTA باستخدام كاشف == Design Of Two New Flow Injection and Sequential Injection Units For Determination Cu (II) Using EDTA and spectrophotometric UV-Vis

Author name: صفا سليم زايد
Supervisor name: خديجة جبار علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص مركبات خماسية وسباعية الحلقة غير المتجانسة من 3- امينو حامض البنزويك == Synthesis and Identification of Five and Seven - Heterocyclic Compounds From 3-Aminobenzoic Acid

Author name: اسيل فاضل كريم الخفاجي
Supervisor name: حسن ثامر غانم
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تصميم منظومة حقن جرياني جديدة تستخدم لتقدير ايون الالمنيوم الثلاثي باستخدام صبغة الاليزارين == Designing A New flow injection unit for determining of Aluminum (III) by Alizarin dye

Author name: زيد نور عبيد الحسيني
Supervisor name: خديجة جبار علي الياسري
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص بعض مشتقات الحلقات السباعية غيرالمتجانسة المشتقة منالايبوبروفين

Author name: ميسلون جواد كاظم
Supervisor name: حسن ثامرغانم
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير ودراسة البلورات السائلة لسلسلتين لمركبات قواعد شف ودراسة الخواص الفيزياوية لها == Preparationand Study of Liquids Crystalline of two Schiff Bases' Compounds Series and their Physical Properties

Author name: عذراء عبد الكاظم وساف الفتلاوي
Supervisor name: ساجدة هادي رضا
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص ودراسة الفعالية الحيوية لليكاندي ازو وقاعدة شف جديدين مشتقة من ثلاثي فلورو مثيل انلين وبعض من معقداتهما الكلابية == Preparation, Characterization and Study of Biological Activity of new azo and Schiff base Ligands Derived From Tri Fluro Methyl Aniline and Some of Their Chelates Complexes

Author name: اسماء عدنان طالب الحسني
Supervisor name: عبد الله محمد علي | عباس حمود محمد علي الخفاجي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

استعمال تقنية الحقن الجرياني بالازواج مع مطيافية فوق بنفسجية المرئية لدراسة معقدات النحاس (II) والزئبق (II) باستعمال الكاشف العضوي الجديد 2-(4- bromo-2,6-dimethyl phenyl ) azo 4,5-diphenyl -1- imidazol) == Use of Flow Injection Technique Coupled with UV-vis spectrophotometre to Study the complexeity of Copper (II) and Mercury (II) Using the New Organic Reagent and Flow Injection Technique 2-(4- bromo-2,6-dimethyl phenyl ) azo 4,5-diphenyl -1- imidazol)

Author name: حيدر نوري رحيم الشكري
Supervisor name: عبد الله محمد علي حبيبان | خديجه جبار علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص معقدات مزيجا لليكاند المشتقة من ليكاند ازو كوينولين جديد == PREPARATION AND IDENTIFICATION OF MIXED LIGAND COMPLEXES DERIVED FROM NEW AZO QUINOLIN LIGAND

Author name: جنان عـزيــز ثابــت
Supervisor name: رحيم طاهر مهدي الساعدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص مركبات حلقية غير متجانسة من قواعد شف ودراسة السلوك الكروماتوغرافي لبعض منها == Synthesis and Identification of Heterocyclic Compounds From Schiff Bases and Study Chromatographic Behavior of Some of Them

Author name: مروة تحسين نعمة
Supervisor name: نغم محمود الجمالي | قاسم كاظم الاسدي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص مشتقات مختلفة للكومارين ودراسة سلوكها بتقنية كروماتوغرافيا غاز - سائل == Synthesis and Characterization of Different Coumarine Derivatives and The Study of its Behavior by Gas - liquid Chromatogeraphy Technique

Author name: حيـدر كـريـم عبـد الكريـطي
Supervisor name: قاسم كاظم الاسدي | فائز عبد الحسين الرماحي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

دراسة امتزاز المضادات الحيوية على سطوح مخلفات الشاي الاسود وقشور الرمان == Study of Adsorption for Some Antibiotics on the Surface of Spent Black Tea Leaves and Pomegranate Peel

Author name: فرح جبار علي الشمري
Supervisor name: سعد عزيز حسن
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

الاستخلاص والتقدير الطيفي لايونات النحاس (II)،الكوبلت (II) والفضة (I) باستخدام تقنية استخلاص نقطة الغيمة في نماذج بيئية وحياتية == Extraction and Spectrophotometric Determination of Cu (II),Co (II) and Ag (I) ions by using Cloud Point Extraction Technique in Environmental and Vital Samples

Author name: شذى سالم طارش الشجيري
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

التبادل الايوني السائل للاستخلاص والتقدير الطيفي لبعض الفلزات على هيئة ايونات سالبة في نماذج مختلفة == Liquid ion Exchange for Extraction and Spectrophotometric Determination of Some Metals as Anion in Different Samples

Author name: نادية مهدي مسلم العميدي
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير متراكبات بوليمرية جديدة من البولي بروبلين ودراسة بعض خصائصها الميكانيكية والفيزيائية == Preparation of new polymeric Composites from Polypropylene and study of Some Mechanical and Physical Properties

Author name: كرار ذياب عبد الكاظم الزيادي
Supervisor name: عامر موسى جودة
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص معقدات مزيج الليكاند لبعض العناصر الانتقالية == Preparation and Characterization of Some Transition Metal Mixed Ligand Complexes

Author name: ايمان جبار جاسم
Supervisor name: عبد الله محمد علي
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير ليكاندين جديدين وتطبيقهمافي استخلاص بعض الايونات الموجبة للعناصر الانتقالية من المحاليل المائية == Synthesis two new Ligands and their application in Extraction of some transition metal cation from aqueous solutions

Author name: فاتن خالد عبود
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

دراسة طيفية لايوني الكوبلت (II) والنحاس (II) باستعمال الكاشف العضوي الجديد 4-(4?- انتي بايرايل ازو ) بايروكالول == Spectrophotometric Study of Cobalt(II) and Copper(II) Ions by Using the New Organic Reagent 4-(4?-antipyriylazo) pyrogallol

Author name: امل سعدون مجيد
Supervisor name: حسين جاسم محمد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير ودراسة طيفية لمعقدات بعض العناصر الانتقالية مع الليكاند الجديدة ذ2-[(3-اسيتايل فنيل)ازو]-4،5-ثنائي فنيل اميدازو

Author name: ندى علي موسى
Supervisor name: عبد الله محمد علي حبيبان
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf

تحضير وتشخيص معقدات بعض العناصر الانتقالية مع ليكاندي ثايوسيميكاربازون جديدتين == Synthesis and Characterization of Some Transition Metal Complexes with Two New Thiosemicarbazone Ligands

Author name: ميثاق سعيد محمد
Supervisor name: عبد الله محمد علي حبيبان
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: تضمن البحث تحضير ليكاندين جديدتين من قواعد شف وذلك بتكاثف الثايوسيميكابازايد مع البنزوين واحدى معوضات الاسيتوفينون التي اعطت الليكاندين الاتيين. 1. بنزوين ثايوسيميكاربازون (L1 = BnTSC).2. بارا - بروبانال اسيتوفنيدين ثايوسيميكاربازون (L2 = p - PrAPTSC). شخصت اليكاندين بالطرائق الطيفية المتاحة باستعمال الاشعة فوق البنفسجية - المرئية والاشعة تحت الحمراء وقياس درجة الانصهار وكذلك التحليل العنصري الدقيق للعناصر. لقد استعملت هاتان الليكاندان في تحضير اثنا عشر معقد كيليتي جديد لكل من ايونات الكوبلت والنيكل والنحاس والخارصين والكادميوم والزئبق الثنائية التكافؤ وقد حضرت هذه المعقدات بعد تثبيت الظروف الفضلى من تركيز مولاري ونسبة مولية وذلك من دراسة اطياف الاشعة فوق البنفســجية - المرئية لمحاليـــل مزج هذه الايونات مع محاليل الليكاندين (BnTSC) و(p - PrAPTSC) كل على حده. شخصت المعقدات الصلبة بعد عزلها طيفيا بوساطة الوسائل الطيفية المتاحة كاطياف (UV - Vis) والاشعة تحت الحمراء (IR). وقد اظهرت محاليلها في الايثانول ازاحة حمراء مقارنة مع محاليل الليكاندين. وعند مقارنة اطياف الـ (IR) لهذه المعقدات مع اطياف الليكاندين الحرة فقد لوحظ تغيرات واضحة اذ اظهرت حزما جديدة لم تكن موجودة اصلا في اطياف الليكاندين في حين عانت حزم اخرى من تغيرات واضحة في الشكل والشدة والموقع وقد يعود السبب في ذلك الى حصول عملية التناسق بين الايونات الفلزية والليكاندين ، تبين منها ان الليكاند (BnTSC) سلكت كليكاند ثلاثية المخلب في حين سلكت (p - PrAPTSC) كليكاند ثنائية المخلب. وبينت نتائج التحليل الدقيق للعناصر (C.H.N) وحساب النسبة المئوية للايونات الفلزية في معقداتها توافقا كبيرا بين النسب المحسوبة نظريا وتلك النتائج المستحصلة عمليا. مما اعطى دعما للصيغ الجزيئية المقترحة. وقد تم استغلال نتائج قياسات (UV - Vis) لحساب النسبة المولية في تعيين ثوابت التكوين (الاستقرار) لهذه المعقدات. في حين استعملت التقنية المذكورة نفسها لمعرفة مدى استقرار المعقدات في محاليلها وبمرور الزمن. وبينت دراسة التوصيلية الكهربائية المولارية لمحاليل المعقدات المحضرة في هذا البحث في مذيبي ثنائي مثيل اوكسيد الكبريت وثنائي مثيل فوماميد وعند التركيز (1×10 - 3) مولاري وفي درجة حرارة المختبر بانعدام الصفة الايونية لهذه المحاليل. اما قياسات الحساسية المغناطيسية للمعقدات فقد بينت ان معقدات الكوبلت (II) والنحاس (II) ولكلا الليكاندين مضافا لمعقد النيكل (II) لليكاند (BnTSC) فانها تمتلك صفات بارامغناطيسية في حين اتصفت بقية المعقدات الكيليتية موضوع الدراسة بالدايامغناطيسية. من كل ما تقدم من نتائج مستحصلة التي تم التوصل اليها فقد تم اقتراح الاشكال الفراغية للمعقدات. | The research includes preparation of two new Schiff bases ligands drived from condensation reaction of thiosemicarbazide with benzoin and substituted acetophenone to give the following ligands : 1. Benzoin thiosemicarbazone (BnTSC = L1). 2. p - propanal acetopheneden thiosemicarbazone (p - PrAPTSC = L2). The identity of these ligands have been characterized by spectral methods (UV - Vis, IR) and another physical properties (m.p.) and elemental analysis. Twelve chelate complexes of two ligands with Co(II), Ni(II), Cu(II), Zn(II), Cd(II), and Hg(II) were prepared and characterized after fixing the optimum conditions of molar concentration and mole ratio using (UV - Vis) technique of mixed solutions of the above ions with (BnTSC) and (p - PrAPTSC ). Electronic spectra of prepared complexes in ethanolic solution showed batho chromic Shift compared with that of free ligands. Thr IR, spectra (using KBr disc) of these complexes showed some charges compared to those of free ligands. New bards were observed indicating that the ligand (BnTSC) is coordinated to the metal ion as atridentate ligand while the other ligand (p - PrAPTSC) coordinated as abidentate ligand. Micro elemental analysis for all complexes were made, the percentage of metal ions were determined using flame atomic absorption spectroscopy. Good agreement was obtained between the found and calculated values. The stability of the complexes in solution were tested by evaluation of (stability formation constants) by electronic spectrum. In addition to determined the stability of there complexes at different time. Conductivity measurement for (DMSO) and (DMF) solutions at (1×10 - 3M) has shown non ionic character for all chelate complexes. Magnetic susceptibility measurements of Co(II) and Cu(II) complexes of both ligands and Ni(II) chelate complex with (BnTSC) show that they are paramagnetic, but the rest complexes show diamagnetic properties. Finally from the observations the geometric structure of the synthesized complexes were suggested

استخلاص نقطة الغيمة بالازدواج مع طريقة طيفية لاستخلاص وتقدير النيكل (??) والكوبلت (??) والبزموث (?I?) في نماذج مختلفة باستعمال مشتقي ازو مناسبين == Cloud point extraction coupled with spectroscopic method for separation, extraction and determination of Nickel( ?? ) , Cobalt( ?? ) and Bismuth ( I?? ) in different samples by use of suitable Azo - derivatives

Author name: احمد صادق عبد هاشم الحمادي
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Analytical Biochemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: Cloud point extraction methodology was used for separation, preconcentration and extraction cations for Bismuth(III) , Nickel(II) , Cobalt(II) as ion association complexes by two new laboratory prepared azo derivatives as complexing agents which are MIBSHA and AADAD as well as these new organic complexing agents studied spectrophotometricaly by UV - Vis spectroscopy and IR specrtrophotometry to confirm their structures and for the separation, preconcentration and extraction of the elements in this study which was performed as follows : 1 - Bismuth(III) Studies : At the beginning an experiment was conducted to determine the wave length of ion association complex of bismuth ion Bi(III) with new laboratory prepared complexing agent MIBSHA by UV - Vis, spectroscopy and the spectrum showed λmax=550nm. Under optimum conditions of extraction Bi(III), the study showed that pHex=9 was more stable for extraction and gave higher efficiency because at this acidic function, there exists the best coordination bounding between Bi(III) and MIBSHA in presence of 40 μg of Bi(III) as optimum concentration giving favorites thermodynamic equilibrium for complex formation and this method of extraction depends on using Non - ionic surfactant 1% Tritonx - 100. And experimental study showed that 0.5ml of this surfactant suitable for forming Cloud point layer (CPL) with higher density and smaller volume to give the best extraction efficiency for Bi(III) with high absorbance and distribution ratio (D). The extraction efficiency also increased with increasing MIBSHA concentration as linear relation because any increasing in MIBSHA concentration is mean increasing in ion pair complex concentration and suitability so increasing in the thermodynamic equilibrium partition to the CPL. And this reflects the sensitivity of new complexing agent MIBSHA in coordination binding and ion pair complex formation in addition to extraction CPE methodology which depends on heating. The experimental study shows that the optimum temperature of heating was (90°C) that gives higher extraction efficiency because it allow to reached the best thermodynamic equilibrium in Cloud point layer formation with good dehydration, as well thermodynamic data was ΔHex=0.145KJ mol - 1, ΔGex= - 73.786KJmol - 1and ΔSex=203.669Jmol - 1K - 1 whereas the low value of enthalpy for Demonstrate extraction to approach another ion of ion pair association complex, also the extraction method is entropic region, and the experimental study about the effect heating time was 20min was the optimum heating time which gives the higher extraction efficiency with high absorbance and distribution ratio D, as this time of heating helps to reach the optimum thermodynamic equilibrium of Cloud point layer formation CPLwith higher dehydration from other hand time of heating indicate the quantity of heat which162is help to dominate on the moving of micelles inside formation cloud point layer CPL with good properties of extraction. Stoichiometric study by using four spectrophotometric methods and the study revealed that the more probable structure of ion pair complex of Bismuth ion Bi(III) extracted was [1 : 1]+ anion [Bi(MIBSHA)]2+;2No3 - experimented study about synergism effect by using Tri butyl phosphate (TBP) and methyl isobutyl ketone (MIBK) show that the extraction efficiency for bismuth ion Bi(III) increased with the presence of TBP or MIBK in aqueous solution by the effect of TBP and MIBK participation in the complex formation of Bi(III) also the experiments showed that there is one molecule of TBP or MIBK enters in the structure of ion pair complex of Bi(III) as [Bi(MIBSHA)(TBP)]2+;2NO3 - ; [Bi(MIBSHA)(MIBK)]2+;2NO3 - and TBP or MIBK enter in the complex instead of water molecule in the hydration shell of Bi(III) and increase hydrophobicity of ion pair complex and increased rate of partitioning to the CPL. As well as this study involved experiments about interferences effects as well as electrolytes effect and these experiments illustrated interferences effect to decline extraction efficiency because these ions form ion pair complex with complexing agent MIBSHA , that means a decrease in complexing agent MIBSHA concentration to form ion pair complex with Bi(III) so that electrolytes affect by increasing extraction efficiency of Bi(III) by effect of increasing Dehydration and destroyed hydration shell of bismuth ion to increase the chances of binding with MIBSHA for more stable ion pair complex. Later, this method was used coupled with suitable spectrophotometric application in the separation and determination of bismuth (III) in different samples.2 - Studies about Nickel (II)For nickel ion Ni(II) extraction from aqueous solution as ion pair complex used new laboratory prepared complexing agent AADAD , the spectrophotometric study for ion pair complex on Ni(II extracted into CPL showed maximum absorbance peak at wave length λmax=585nm and through the experimental study to limit optimum conditions and effective parameters. The study demonstrated that the optimum pHex was (9) which gives the highest extraction efficiency for nickel ion Ni(II by use complexing agent AADAD, whereas at this pHex favorable binding was given to form ion pair complex of nickel ion Ni(II with high concentration and stability as well as the method CPE for extraction Ni(II needed 0.5ml of non - ionic surfactant 1% TritonX - 100 which is affected to reach favorable thermodynamic equilibrium for aggregation of micelles in the state CMC for CPL formation with good163properties for the ion pair complex extraction of Ni(II) as well this extraction efficiency appeared with the presence of 50μg Ni(II) in aqueous solution to reach the best thermodynamic equilibrium for ion pair complex formation. Increasing AADAD concentration showed the existence of linear relation with linear increase in absorbance and distribution ratio and linear increasing in concentration stability and partitioning to CPL ion pair complex of Ni(II whereas CPE methodology depends on the temperature of heating, the experiment showed that 80°C was the optimum temperature that gives the higher extraction efficiency of Ni(II with thermodynamic data ΔHex= 0.1126KJmol - 1 , ΔGex= - 58.19KJmol - 1 and ΔSex=165.16Jmol - 1K - 1 . These values prove that the ions of ion pair complex for Ni(II) extracted into CPL approached one another with a high gegree and the method of extraction was entropic in region. The experimental study about the effect of heating time showed that 15min was the best time of heating that allows to reach a higher extraction efficiency of CPE method. Time of heating indicates the kinetic side of extraction method as heating for 15min at 80°C gave the quantity of heating that hels to reach the favorable thermodynamic equilibrium for CPL formation stoichiometry showing the more probable structure of ion pair complex extracted for Ni(II) which was [Ni(AADAD)]+;No3 - but synergism effect study showed that by using TBP and MIBK showed increasing extraction efficiency of Ni(II) with the presence of TBP or MIBK in aqueous solution because substitution water in coordination shell of Ni(II) in ion pair complex and effect to increase hydrophobicity, stability and partitioning to CPL. Also, the study revealed that adding one molecule of TBP or MIBK in the structure of ion pair complex of Ni(II) such as [Ni(AADAD)(TBP)]+;NO3 - , [Ni(AADAD)(MIBK)]+;NO3 - . So the studies tackled the effect of interferences as cations and electrolytes on extraction efficiency, later on, we used this method in the extraction and spectrophotometric determination of Nickel (II) in different samples.3 - Studies about Cobalt (II)The experimental studies concerning the separation, preconcentration and extraction of cobalt(II) as ion association complex by using the same complexing agent used with nickel (II) AADAD according to Cloud point extraction methodology. The UV - Vis spectrophotometric studies about the ion association complex extracted showed that the maximum absorbance of the complex of wave length λmax=530nm. As well as the extraction method according to CPE method showed (pH=8) was the optimum acidic function for extraction giving the highest absorbance and distribution value D because this pHex the best164coordination bonding between cobalt ion Co(II) and complexing agent AADAD so that high partitioning of stable complex to cloud point layer CPL. Moreover, the experiments showed that 0.5ml of Non - ionic surfactant, very stable for giving higher extraction efficiency because this volume of surfactant helps to reach the favorable thermodynamic equilibrium of aggregation of micelles to form CPL with high density and small volume and the micelles in case one approaches the other with the best dehydration to be in high hydrophobicity with good partitioning of complex to CPL. And in this case giving higher extraction efficiency, also, this extraction efficiency obtained when 60μg of cobalt ion Co(II was in the aqueous solution to give the best thermodynamic equilibrium to formation high stability ion pair complex extracted into CPL quantitively effect of temperature study showed that 80°C was the best temperature of extraction according to CPE method because in this temperature the best CPL was formed by aggregation and using dehydration at CMC state happen good extraction as well as thermodynamic data for extraction Co(II) was ΔHex=0.1014KJmol - 1, ΔGex= - 60.658KJmol - 1, ΔSex=171.86Jmol - 1K - 1. These data showed from the small positive value of enthalpy of extraction , the ions of ion pair complex extraction when one approach another to increase stability of this complex as well the large positive value of entropy of extraction demonstrates the dependence of extraction according to CPE and entropy. Then this procedure being entropic in region. Time of heating as the experiment study showed is 15min and was stable to give higher extraction efficiency. Because heating the solution at fixed temperature and time mean the quantity of heating help kinetically to reach thermodynamic and kinetic equilibrium for formation CPL. Then giving higher extraction efficiency. Stoichiometry study revealed that the more probable structure of ion pair complex extracted was [Co(AADAD)]+;NO3 - . Synergism study show presence TBP or MIBK in aqueous solution effect to increase extraction efficiency of Co(II) according to CPE method. Because complexing agent AADAD was not able to saturated the coordination shell of Co(II) ion in complex formation then the empty coordination position and occupy with water molecule and decline extraction efficiency , but TBP or MIBK able to coordinate instead of water in coordination shell and increase extraction efficiency, as well the study showed one molecule of TBP or MIBK able to enter in complex formed such as [Co(AADAD)(TBP)]+;NO3 - or [Co(AADAD)(MIBK)]+;NO3 - . So that the studies involved the effect of interferences as cations and electrolytes on extraction efficiency , later we used this method for the extraction and spectrophotometric determination of cobalt (II) in different samples.

تحضير ودراسة الفعالية الحيوية لبعض مشتقات السلفايد والسلفون == Synthesis , Identification and Biological Activity for (Sulfide ,Sulfone) - Compounds

Author name: رشا نعمة حسين الجعباوي
Supervisor name: نغم محمود جواد الجمالي
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: Sulfone and Sulfide are important compounds due to their uses in industrial , artificial and pharmaceutical applications . They are characterized by their effectiveness against skin diseases and fungal what make them used as biologically important substances and preparatory studies have been extended to their derivatives. The research includes two sections : Section I : : contains preparing 19 compound which are (R1 - R19) in six parts : : - Part one : - includes preparing compound (R1) from the interaction of (Thio semicarbazide) with (Diethyl Terephthalate) interacting the resulted (R1) react with (10% Sodium hydroxide ) to prepare the compound (R2), interacting the resulted compound with (chloro ethyl acetate) to prepare the compound (R3) , and finally interacting the resulted compound with acetic acid and hydrogen peroxide to prepare compound (R4). Part two : - includes preparing compound (R5) by interacting compound (Sulfobenzoic anhydride) with (2 - amino - 5 - mercapto - 1,3,4 - thiadiazole) then the resulting interaction (R5) with( chloro ethyl acetate) to prepare the compound (R6) , and interacting the result with (acetic acid) and (hydrogen peroxide) to prepare compound (R7).Part three : - : includes preparing compounds (R8, R9, R10) by interacting (phenylene diamine) with (2 - mercapto acetic acid) to produce (R8) and reactance of this compound with Formaldehyde)) to form a compound (R9) and interacting the last compound (acetic acid) and (hydrogen peroxide) to prepare compound (R10). Part four : - includes interacting (2 - amino - 5 - mercapto - 1,3,4 - thiadiazol) with a compound formaldehyde)) to prepare the compound (R11) , interacting compound R11 and interacting the result with (Sulfobenzoic anhydride to produce compound (R12). Part five : - : includes preparing compounds (R13,R14, R15, R16) by interacting compound (Formaldehyde) with (2 - mercapto benzoic acid) to form (R13) , and interacting this result with ( Thio semicarbazide)) and (sodium hydroxide 10%) for the preparation of R14)), which through its interaction with (chloro ethyl acetate) is the preparation of the compound (R15 The oxidizing the resulted compound by (acetic acid) and (hydrogen peroxide) , gives (R16). Part six : - includes preparing compound (R17) by interacting( 2 - mercapto benzoic acid)) with(3 - chloro propanoyl chloride) and interacting the finally with (Thio semicarbazide) give (R18), which we can obtain011compound (R19) by interacting with (chloro ethyl acetate).All the prepared compounds have been following up the interactions enabled chromatography thin layer (TLC) for each prepared vehicles and characterized by (IR) spectrum NMR proton (1H.NMR), and a nice nuclear magnetic resonance of carbon (13C.NMR) and (C.H.N), and then measure the degree of fusion.Section II : This section includes the study of the biological inhibitory action to some of the prepared compounds on positive bacteria for dye Gram (Staphylococcus aureuse) and another negative bacteria for dye Gram (Escherichia Coli). All the compounds showed effect against both selected bacteria in the study.The Scheme below clarifies

تحضير مركبات الكبريت غير متجانسة الحلقة ودراسة الفعالية الحيوية لبعض منها == Synthesis Sulfur Heterocyclic Compounds and Study Biological Activity for Some its

Author name: انتصار عبيد سلمان الفتلاوي
Supervisor name: نغم محمود جواد الجمالي
General topic: Chemistry
Specific topic: Organic Chemistry
Degree: Master
Language: Arabic
University location: Najaf
Key words:
  • الثايازول، الثيادايازول
  • الثايازين
  • الثايادايازين
  • الثايازبين
  • الثيادايازبين
First pages:
Abstract: The compounds of heterocyclic that have the qualities of a great biological and pharmacological importance, where we see through the growing literature in Chemistry published research in this area significantly, so we decided to prepare new derivatives of them.In this study prepared (16) a new deriva????ve of sulfur heterocyclic compounds such as Thiazole, Thiadiazole Thiazine, Thiadiazine, Thiazepine and Thiadiazepine, and three other intermediate compounds to prepare Some of these derivatives, these compounds ((Five, Six and Seven - Membered Heterocycles))The research included two Section of study : The first section : included prepara????on (19) compounds (I1 - I19), by four parts : The first part : included preparation (I1) of benzil interaction with thiosemicarbazide and then the interaction of output with nitrous acid record spontaneously from mixing hydrochloric acid with sodium nitrite, to form a diazonium salt and then reactance this salt with (Acetyl acetone) to prepare azo compound (I2), and Then reactance output with thiourea, thiosemicarbazide, Thioacetamide and cysteine respectively for the preparation of compounds (I3 - I6).The second part : included reactance (diethyl terephthalate) with thiosemicarbazide, cysteine to prepare the compound (I7) and compound (I9), respectively, and then reactance outputs with Sulfobenzoic anhydride, thiosemicarbazide respectively to produce the compound (I8) and compound (I10), respectively. The third part : included reactance (1,3 - diphenylpropane - 1,3 - dione) with thiosemicarbazide to give the compound (I11) and then output reactance with benzaldehyde to give the compound (I12) and then output with reactance Sulfobenzoic anhydride to give the compound (I13). The fourth part : includes reactance (p - amino acetophenon)with nitrous acid record spontaneously from mixing hydrochloric acid with sodium nitrite, to form a salt of diazonium and then reactance this salt with diethyl mal Acetyl acetone to give compound (I14) and compound (I17), respectively, and then reactance thiosemicarbazide, benzaldehyde respectively, to give the compound (I15) and compound (I18), respectively, and then outputs reactance with Sulfobenzoic anhydride, thiourea to give compound (I16) and compound (I19), respectively. All interactions followed up by thin layer chromatography (TLC) for each prepared compounds and diagnosed by spectrum infrared (FT.IR) spectrum, proton nuclear magnetic resonance (1H.NMR), nuclear magnetic resonance of carbon (13C.NMR) and Elemental Analysis(C.H.N), and then measure the melting point. The second section : This section of the research included the study of the inhibitory action of the some of biological compounds against the gram - positive bacteria (Staphylococcus aureuse) and gram - negative bacteria (Escherichia coli) and all showed the effectiveness of the compounds against selected bacteria in the study type.

تحضير وتشخيص ليكاندات قواعد شيف مشتقة من الترفثالديهايد ودراسة معقداتها مع بعض العناصر الفلزية == Synthesis And Identification of Schiff Bases Ligands Derived From Terephthaldehyde And Studying Its Complexes With Some Metal Elements

Author name: علي محمود علي
Supervisor name: محمد حامد سعيد | حسن ثامر غانم
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: This thesis studies the synthesis of three new Schiff base ligand (L1 , L2 ,L3 ) derived from terephthaldehyde, the first ligand (L1) is produced by the reaction of terephthaldehyde with ortho - phenlenediamineat ( 1 : 2) molar ratio.The second ligand (L2) is produced by the reaction of terephthaldehyde with ortho - phenlenediamine at ( 2 : 1) molar ratio. The third ligand (L3) is produced by the reaction of terephthaldehyde with 2 - aminobenzothiazol at (1 : 1) molar ratio .These ligands are identified by using FT - IR and Uv - Vis spectroscopies,1H - NMR, massspectrometer and elemental analysis.These ligands are mixed with some metal chloride solutions Co(II), Ni (II), Cu(II) and Zn(II) by using absolute ethenolic solutions at (2 : 1) molar ratio to formtwelve complexes . These complexes are identified byanalytical andspectroscopic techniquessuch as elemental analysis andthe determination of the metalratio within its complex, recording infrared spectra,in addition to Uv - Vis by useing solvent DMSO (1x10 - 4M), the same solvent is used with molar conductance measurements for solutions of compounds at(1 x 10 - 3M)at room temperature, in addition to measuring the magnetic sensitivity of the complexes in solid state .This study has concluded that by using all the above techniques and experiments ,all these ligands' have acted as bidentate to form pentagonal and tetragonal metal cycles .Depending on the results of the study,octahedral structures of all the prepared ligands' complexes have been suggested.The following stereochemistriesreflect the complexes which are the subject of the study

فصل واغناء بواسطة الاستخلاص بنقطة الغيمة والتقدير الطيفي لـ (??) Mg و(??) Zn و(??) Hg في نماذج تحليلية == Separation and Preconcentration by Cloud Point Extraction and Spectrophotometric Determination for Mg(??), Zn(??) and Hg(??) in Analytical Samples

Author name: فارس حــميد حــيدر الــحيدري
Supervisor name: شوكت كاظم جواد
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: استخدمت تقنية استخلاص نقطة الغيمةCloud point Extraction (CPE) في فصل واستخلاص واغناء كل من ايون الخارصين(II) والمغنيسيوم(II) والزئبق(II) من المحاليل المائية بالازدواج مع طرق طيفية لمطيافية(UV - Vis spectroscopy) لتقدير هذه العناصر قيد الدراسة وذلك باتباع تقنية تكوين معقد الترابط الايوني او المعقد الكيلتي لايون الخارصين(Zn2+)، مع كاشف عضوي جديد محضر مختبريا هو(AIBSNB)، واما كل من ايون المغنيسيوم(Mg2+)، وايون الزئبق(Hg2+) فقد استخلص وفق مبدا التمذوب(solvation) باستخدام(2,4 - dimythyl pentane - 3 - one) للمغنيسيوم(Mg2+)، و(Acetophenone) بالنسبة للزئبق(Hg2+).بينت الدراسة ان ايون الخارصين استخلص على هيئة معقد ترابط ايوني (Ion association complex) او معقد مخلبي(Chelate complex) بالارتباط مع الكاشف (AIBSNB) الجديد والمحضر مختبريا والذي اجريت له دراسة طيفية بمطيافية فوق البنفسجية - المرئية (UV - Vis spectroscopy) ومطيافية تحت الحمراء (IR - spectroscopy) وكذلك التحليل الدقيق للعناصر وقد اثبتت الدراسات الطيفية وتحليل العناصر صحة التركيب المقترح للكاشف العضوي الجديد(AIBSNB) كما ان الدراسة الطيفية للمعقد المستخلص للخارصين(II) مع الكاشف العضوي(AIBSNB) بمطيافية(UV - Vis spectroscopy) اثبتت ان الطول الموجي لاعظم امتصاص للمعقد كان(λmax=380nm)، وقد اوضحت الدراسات لاستخلاص الخارصين(II) ان قيمة الدالة الحامضية المثلى لعملية الترابط وتكوين المعقد المستخلص كانت(pHex=9) عند وجود(50µg) من ايون الخارصين (Zn2+) في 10mL من المحلول المائي. وقد اثبتت التجارب العملية ان استخلاص ايون الخارصين على هيئة معقد ترابط ايوني او مخلبي وفق تقنية استخلاص نقطة الغيمة (CPE)يحتاج الى تسخين عند درجة حرارة(90ºC) ولزمن مقداره(15دقيقة)،فقد اظهرت الدراسة قيم الدوال الثرموديناميكية لاستخلاص الخارصين(II) هي(Sex=+155.9400 J mol - 1K - 1∆)، (Gex= - 56.4830 kJ mol - 1∆)، (Hex= +0.1242 kJ mol - 1∆)، كما تبين ان (0.5mL) من المادة النشطة سطحيا (surfactant) (TritonX - 100 1%) كانت هي الافضل في عملية الاستخلاص حيث تكون طبقة نقطة الغيمة(CPL) ذات الكفاءة العالية للاستخلاص. كما شملت الدراسة تحديد التركيب الاكثر احتمالا للمعقد المستخلص لايون الخارصين، وذلك باتباع اربعة طرق طيفية من اجل ذلك وقد اشارت هذه الطرق الى ان المعقد المستخلص كان له التركيب [Zn(AIBSNB)]+;NO3─ او [Zn(AIBSNB)+(NO3)─] كما ان دراسة توليف المذيب(Synergism) لاستخلاص الخارصين(Zn2+) بينت ان هناك مشاركة لجزيئة واحدة من كل من(TBP) و(MIBK) في تكوين المعقد المستخلص لايون الخارصين(Zn2+) يرافقه زيادة كبيرة في كفاءة الاستخلاص. وقد تضمنت الدراسة توضيح اثر بعض المتداخلات وكذلك الاملاح الالكتروليتية وتاثيرها على كفاءة استخلاص ايون الخارصين(Zn2+)، كما استخدمت طريقة الاستخلاص هذه في اجراء عمليات فصل وتقدير الخارصين في نماذج بيئية وحياتية مختلفة.تمت عملية استخلاص وتقدير ايون المغنيسيوم(II) وايون الزئبق(II) باستخدام طريقة استخلاص نقطة الغيمة (CPE) وباستعمال المادة النشطة سطحيا (surfactant) (1% TritonX - 100) ووفق تقنية التمذوب(solvation)، وباستعمال مركب(2,4 - DMP) (2,4 - dimythyl pentane - 3 - one) ، كعامل استخلاص (Extractant) للمغنيسيوم(II)، وكذلك(Acetophenone) كعامل استخلاص للزئبق(II) وقد اشارت الدراسة الى ان الصنف المستخلص لايون المغنيسيوم(II) كان له اعلى قمة امتصاص عند(λmax=249nm)، اما الصنف المستخلص لايون الزئبق(II) كان له اعلى قمة امتصاص عند(λmax=293 nm). بينت عملية استخلاص كل من ايون المغنيسيوم(Mg2+) وايون الزئبق(Hg2+) وفق مبدا التمذوب(Solvation) تحتاج الى استخدام عامل التمليح (Salting out Effect) وقد استخدم(KNO3) كعامل تمليح وقد اعطى اعلى كفاءة استخلاص لايون المغنيسيوم(Mg2+) عند(0.5M) اما اعلى كفاءة استخلاص لايون الزئبق(Hg2+) كانت عند تركيز عامل التمليح(KNO3) بمقدار(0.08M) وبوجود(50µg) من كل من ايون المغنيسيوم(Mg2+) وايون الزئبق(Hg2+) حيث ان هذا التركيز لايون(Mg2+) و(Hg2+) يعطي افضل توازن ثرموديناميكي لتكون الصنف المستخلص لايون(Mg2+) وكذلك(Hg2+) وفق مبدا التمذوب (Solvation). كما تضمنت الدراسة استخدام انواع مختلفة من عوامل التمليح وبتراكيز مختلفة، حيث تبين ان كفاءة استخلاص المغنيسيوم(Mg2+) والزئبق(Hg2+) وفق مبدا التمذوب (Solvation) يختلف باختلاف نوع عامل التمليح واكثر من تاثره بتركيز عامل التمليح. كما ان تقنية استخلاص نقطة الغيمة(CPE) لفصل الصنف المستخلص لايون المغنيسيوم(Mg2+) وايون الزئبق(Hg2+) اوضحت انها تحتاج الى تسخين لدرجة حرارة (90ºC) لايون المغنيسيوم(Mg2+)، و(85ºC) لايون الزئبق(Hg2+) وبزمن تسخين مقداره(15دقيقة) لكلا الايونين وعند وجود(0.5mL) من المادة النشطة سطحيا(surfactant) (TritonX - 100 1%) لكلا الايونين ايضا. كما شملت الدراسة استخدام عدد من عوامل الاستخلاص المختلفة وبيان تاثيرها على كفاءة الاستخلاص لايون المغنيسيوم(Mg2+) وايون الزئبق(Hg2+) وفق مبدا التمذوب(Solvation)، مركب(Acetophenone) هو الافضل والاكفا في استخلاص ايون المغنيسيوم(Mg2+) وايون الزئبق(Hg2+) على حد سواء وقد اشارت طريقة استخلاص نقطة الغيمة (CPE) لفصل واستخلاص واغناء كل من المغنيسيوم (Mg2+) والزئبق (Hg2+) وفق مبدا التمذوب (Solvation) ان قــــــــــيم الـــــــدوال الـــــثرموديناميكية لــــــــــعملية الاســـــــــــتخلاص كانت(Sex= +173.2830 J mol - 1K - 1∆)، (Gex= ─ 63.1314 kJ mol - 1∆) (Hex= +0.2295 kJ mol - 1∆) لايون المغنيسيوم (Mg2+) اما لايون الزئبق (Hg2+) فقد كانت الــــــــــدوال الـــــــــــــــــثرموديناميكية للاستخلاص هي (Sex= +202.6789 J mol - 1 K - 1∆) ، (Gex= ─ 72.4139 kJ mol - 1∆) ، (Hex= + 0.14521 kJ mol - 1∆) وقد طبقت هذه التقنية في استخلاص وتقدير(Mg2+) والزئبق(Hg2+) في نماذج بيئية وحياتية مختلفة. | Absract By used of cloud point extraction method for sepration, extraction and preconcentration for Zn(II), Mg(II) and Hg(II) from aqueous solutions copuled with spectrophotometric UV - Vis methods to determenation . these elements in environmenteal and vital sampels, with using of laboratory prepared new organic reagent (AIBSNB) for extraction Zn2+ as complex but Mg2+ and Hg2+ extracted by CPE method according to solvation technique by (2,4 - dimethyl pentan - 3 - one) (2,4 - DMP) for Mg2+ and (Acetophenone) for Hg2+.The study show extracted Zinc ion Zn2+ as ion association complex or cheleate complex after coordinat biding with organic reagent (AIBSNB), which is new laboratory prepared and the spectroscopic stadies for this new organic reagent demonstrate the true suggestion of it is structure, as well as spectrophotometric study for complex of this organic reagent with Zinc ion Zn2+ extracted to CPL in CPE method show maximum absorbance wave length was λmax=380nm. The study of extraction Zn2+ appear pH=9 was the optimum acidic function for aqueous phase in presence 50μg Zn2+ in 10mL aqueous solution and the experiments for extraction Zn2+ as ion association complex or chelate complex according to CPE method need heating the solution to 90ºCfor 15mintes time of heating. And the thermodynamic data for extraction was (∆Sex=+155.94 J mol - 1K - 1), (∆Gex= - 56.483 kJ mol - 1), (∆Hex=+0.1242 kJ mol - 1), whereas the study show (0.5mL) of surfactant (1% TritonX - 100) was the optimum concentration of non ionic surfactant to formation cloud point layer (CPL) as second aective phase for extracted complex of Zn2+, in addition to the study ivolved determine the more probable structure of complex extracted by used foure spectrophotometric studies which was appeared the complex extracted for Zn2+ was[Zn(AIBSNB)]+;NO3 - or [Zn(AIBSNB) - (NO3 - )], so that synergism study show there is aparticipate for one molecule of TBP or MIBK in the formation of complex Zn2+ extracted with increasing in extraction efficiency for Zn2+ . from the other hard used this method for separation and determination Zn(II) in envirommental and vital samples.But extraction and determination megnesium(II) and mercury(II) by CPE methodology with using of nonionic surfactant 1% TritonX - 100, and according to solvation technique by use of (2,4 - dimethylpentan - 3 - one)(2,4 - DMP) as extractant for Mg(II) so Acetophenoe as extractant for Hg(II).The study was show the extracted species for megnesiumion Mg2+ has maximum absorbance at wave length λmax=249nm and extracted species for mercury ion Hg2+ has maximum absorbance at wave lengthλmax=293nm, as well as extraction Mg2+ and Hg2+ according to this method (solvaton) needed salting out then used KNO3 as salting out and giving higher extraction efficiency at 0.5M KNO3 for extraction Mg2+,but for extraction Hg2+ used 0.08M KNO3 to giving higher extraction efficiency in pressence 50μg Mg2+ and Hg2+ each one alone. As optimum concentration ,whereas this quantity from metal cation help to reached farorable thermodynamic equilibrium for formation extracted spesies for Mg2+and Hg2+according to solvation method. Also this study demonstrate different salting out and different concentration, and show extraction efficincy for Mg2+and Hg2+according to solvation method differ by kind of salting out more than it is concentration, as well extraction the species of Mg2+ and Hg2+ by CPE method reached high efficiency by heating at 90ºC for Mg2+ and at 85ºC for Hg2+ with heating time 15 minutes for both ion in precence (0.5mL) of 1% TritoX - 100 so that study the effect of different extractant on extraction efficiency of Mg2+ and Hg2+according to solvation method.Thermodynamicaly extraction of thes ion by solvation method show thermodynamic data was(∆Sex=+155.94 J mol - 1K - 1), (∆Gex= - 56.483 kJ mol - 1), (∆Hex=+0.1242 kJ mol - 1), for Mg but for Hg2+thermodynamic data was (∆Sex=202.6 J mol - 1K - 1), (∆Gex= - 72.4138 kJ mol - 1), (∆Hex=0.1421 kJ mol - 1), this study involved determination Mg(II) and Hg(II) in different samples according to solvation method by CPE technique.

حماية الفولاذ الكاربوني المستعمل في افران معمل اسمنت الكوفة من التاكل == Protection of Carbon Steel used in Kufa Cement Plant Kilns from Corrosion

Author name: علي كاظم هادي الشماع
Supervisor name: سعد عزيز حسن حسوة
General topic: Chemistry
Specific topic: Chemistry
Degree: Master
Language: Arabic
University location: Najaf
First pages:
Abstract: يتناول موضوع الرسالة دراسة تاكل الفولاذ الكربوني(ST37 - 2)في محلول حامض الكبريتيك ذوالتركيزين(5x10 - 3M,2.5x10 - 6M)ومحلول هيدروكسيدالصوديوم(3.5x10 - 6 M) في المدى الحراري التجريبي من(303الى333)كلفن وباستعمال جهاز المجهاد الساكن (potentiostat ) وبدا مسح الجهد لمدة 20 دقيقة بعد غمر الانموذج من الفولاذ الكربوني في محلول التاكل بدءامن - 300 ملي فولت ومتابعة التفاعل لحين بلوغ الجهد +300 ملي فولت مقابل قطب الكالوميل المشبع وكان معدل تغير جهد المجهاد الساكن مع الزمن يصل الى30ملي فولت لكل دقيقة واستعمل هذا المعدل لتسجيل كثافة التيار بصورة مستمرة مع تغير الجهد.ولقد تم ايجاد كثافات تيار التاكل, جهود التاكل وكذلك خطوط ميل تافل الكاثودية والانودية من منحنيات الاستقطاب في محاليل التاكل. واظهرت النتائج العملية الى انزياح جهود التاكل الى قيم اكثر سالبيه مع ارتفاع درجة الحرارة, كما وازدادت كثافات تيار التاكل عموما مع ارتفاع درجات الحرارة مشيرة الى زيادة سرعة التاكل مع زيادة درجة الحرارة .الاجزاء المستقيمة لخطوط تافل الكاثودية والانودية انزاحت دوما بصورة متوازية لبعضها البعض.حافظت خطوط تافل على خطيتها وبقي مقدار التغير في ميلها طفيفا في كل الدرجات الحرارية التجريبية وهذا دليل على عدم حصول تغيير في ميكانيكيات التفاعلات الكاثودية والانودية مع تغير درجة الحرارة, وامكن الاستدلال من قيم ميل خطوط تافل على ان تعادل ايونات الهيدروجين على المواقع الكاثودية وذوبان الفلز من المواقع الانودية هي الخطوات السائدة والمقررة لسرع التفاعلات التي حدثت على السطوح البينية لكل من الكاثود/ محلول والانود / المحلول . واستنتجت معلومات الدينمية الحرارية لعملية التاكل من قيم جهود التاكل اذﹾ بينت النتائج عموما امكانية حدوث تفاعلات التاكل ورافق تكوين نتاجات التاكل تغيرات في كل من انثالبي وانتروبي التاكل. كما بينت المعلومات الحركية على حدوث تاثير التعويض في تفاعل التاكل، وكما اشارت قيم كل من الطاقة الحرة والانتروبي لعملية التاكل في الاوساط المختلفة الى ان تفاعل التاكل يكون تلقائيا مصحوبا بزيادة في قيم الانتروبي ضمن الظروف التجريبية .اما قيم دوال الدينمية الحرارية لعملية تثبيط التاكل وباختلاف الصبغات المستعملة في الدراسة فكانت مختلفة اعتمادا على طبيعة المثبط اذ تراوحت قيم كل من انثالبي الامتزاز وانتروبي الامتزاز بين الموجبة والسالبة اما طاقة جبس الحرة لعملية الامتزاز فكانت موجبة لجميع المثبطات.اما بالنسبة لكفاءة التثبيط فكانت كمايلي : ا - صبغة الـ (Murexide) اظهرت اعلى كفاءة تثبيط في الوسط 2.5x10 - 6 M H2SO4 اذ تجاوزت .998%عند استعمال تركيز 5 ppmوضمن المدى الحراري التجريبي333 - 303 K . ب - صبغة الـ (Sudan III) اظهرت اعلى كفاءة تثبيط 99.6% في الوسط 2.5x10 - 6 M H2SO4 عند استعمال تركيز 150 ppm وبدرجة حرارة 313 K . ت - صبغة الـ (Carmine) اظهرت اعلى كفاءة تثبيط 99.4% في الوسط 2.5x10 - 6 M H2SO4 عند استعمال تركيز 25 ppm وبدرجة حرارة 333 K . ث - صبغة الـ (Leishman) اظهرت اعلى كفاءة تثبيط في الوسط 2.5x10 - 6 M H2SO4 عند استعمال تراكيز 50,25,5 ppm وبدرجة حرارة 333 K اذ بلغت 99.5%.وبصورة عامة امكن استنتاج اعلى كفاءة تثبيط للاصباغ الاربعة في محاليل التاكل وضمن المدى الحراري التجريبي وكمايلي : محلول 10 - 3 M H2SO4) x5Murexide ˃ Leishman ˃ Sudan III ˃ Carmine (محلول 10 - 6 M H2SO4) x2.5Leishman ˃ Sudan III ˃ Carmine ˃ Murexide (محلول 10 - 6 M NaOH) x3.5Leishman ˃ Sudan III ˃ Carmine ˃Murexide (تم استعمال مجهر الالكتروني المسحي في دراسة التركيب البلوري لعينة الفولاذ الكربوني (ST37 - 2) بعد تعرضه للتاكل بغياب اية صبغة وعند وجود تركيز 50 ppm من كل صبغة من الصبغات الاربعة قيد الدراسة وبدرجة حرارة40oC وفي محلول حامض الكبريتيك ذو التركيز 2.5x10 - 6M H2SO4 كانموذج للفحص المجهري ، وتبين من الدراسة المجهرية ان التاكل الذي يصيب الفولاذ الكربوني ST37 - 2 هو من النمط الذي يصيب الحبيبات البلورية الاوستنيتية والفريتية التي يشتمل عليها الفولاذ الكربوني، فضلا عن تاكل الفواصل البلورية | The subject of this thesis concerned with the investigation of the polarization behaviour of the carbon steel (ST37 - 2) specimen in (5x10 - 3 M H2SO4 ,2.5x10 - 6 M H2SO4 and 3.5x10 - 6 M NaOH ) solutions over the temperature range(303 - 333 K).The potential scan about 20 minute after the specimen immersion in the solutions beginning at - 300mV and proceed through to +300mV verses a saturated calomel electrode .Four dyes (Carmine , Murexide , Leishman and Sudan III ) dyes were used as corrosion inhibitors at concentrations ranging from (5to150 ppm).The corrosion current densities iCorr , corrosion potentials ECorr ,the cathodic and anodic Tafel slopes have been derived from the polarization curves of the carbon steel specimen in the studied solutions with and without dyes. An attempt was made to estimate on theoretical treatments the thermodynamics functions of corrosion of carbon steel (ST37 - 2). The kinetics of corrosion and inhibition of the carbon steel specimen have also been studied by measuring the corrosion rates in presence and absence of dyes (inhibitors) at several temperatures in the experimental temperature range. In general the results of the corrosion experiments showed a shift of the corrosion potentials towards more negative values with the rise of temperatures.The corrosion current densities generally increased with the rise of temperature reflecting the increasing rate of carbon steel (ST37 - 2) specimen corrosion with increasing temperature .The linear sections of the cathodic Tafel lines shifted almost to each other ,and a similar behaviour was found for the linear sections of the anodic Tafel lines .The Tafel lines maintained their linearity and slope at all experimental temperatures suggesting no alterations in the mechanisms of the cathodic and anodic reactions with the variation of temperature .The values of the Tafel slopes suggested that the proton discharge at the cathode and the metal dissolution at the anode were the prevailing rate determining - steps of the reactions which occurred at the cathode /solution and anode / solution interfaces .The measured corrosion potentials and current densities enabled a thorough investigation of the thermodynamic and kinetic aspects of the carbon steel (ST37 - 2) corrosion in the studied solutions. Thermodynamics of carbon steel (ST37 - 2) specimen corrosion have been deduced from their corrosion potentials and the resulting data showed the generally the feasibility of the corrosion reactions and that the formation of the corrosion products was accompanied by the variation of the enthalpy values between negative and positive values and increase of the entropy values of corrosion with variation of temperature . The kinetic data showed the operation of a compensation effect in the corrosion reaction of carbon steel(ST37 - 2) . Also thermodynamics of the dyes adsorption process (inhibition process) in different temperatures were calculated ,the resulting data shows the values of enthalpy and entropy of adsorption ranged between positive and negative values while the values of Gibbs free energy of the adsorption process were positive for all dyes. As for the inhibition efficiency was found as follows : A. Murexide dye was acted as good inhibitor in 2.5 x10 - 6 M H2SO4 and showed the highest inhibition efficiency reach to 99.8% when using concentration of 5 ppm of dye and within the temperature range 333 - 303 K. B. Sudan III dye showed the highest inhibition reach to 99. 6% in 2.5 x10 - 6 M H2SO4 concentration when 150 ppm of dye used and at temperature of 313 K. C. Carmine dye showed the highest inhibition efficiency reach to 99.4%in2.5x10 - 6MH2SO4when using 25 ppm of dye and at temperature of 333 K. D. Leishman dye showed the highest inhibition efficiency in 2.5 x10 - 6MH2SO4at dye concentrations of 50,25,5 ppm and at temperature of 333 K . In general the tendencies of the four dyes for corrosion efficiency followed the orders : 5x10 - 3 M H2SO4 ) Murexide ˃ Leishman ˃ Sudan III ˃ Carmine ( 2.5x10 - 6 M H2SO4) Leishman ˃ Sudan III ˃ Carmine ˃ Murexide (Leishman ˃ Sudan III ˃ Carmine ˃Murexide ( 3.5x 10 - 6 M NaOH) Electronic scanning microscopy was used to study the Crystal structure of a carbon steel(ST37 - 2)specimen after being subjected to corrosion in the absence of dye and presence in a concentration of 50ppm of each dye and at temperature of 40oC and in a solution of sulfuric acid with a concentration of 2.5 x10 - 6 M H2SO4 as a sample for microscopic examination, the microscopic study found that corrosion of carbon steel (ST37 - 2)is of the style of the Austenitic and ferritic Crystal grains as well as crystal boundary corrosion
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