Analytical Chemistry
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Chemistry Grade Level 10 Units 1-15
COPPELL ISD SUBJECT YEAR AT A GLANCE GRADE HEMISTRY UNITS C LEVEL 1-15 10 Program Transfer Goals ● Ask questions, recognize and define problems, and propose solutions. ● Safely and ethically collect, analyze, and evaluate appropriate data. ● Utilize, create, and analyze models to understand the world. ● Make valid claims and informed decisions based on scientific evidence. ● Effectively communicate scientific reasoning to a target audience. PACING 1st 9 Weeks 2nd 9 Weeks 3rd 9 Weeks 4th 9 Weeks Unit 1 Unit 2 Unit 3 Unit 4 Unit 5 Unit 6 Unit Unit Unit Unit Unit Unit Unit Unit Unit 7 8 9 10 11 12 13 14 15 1.5 wks 2 wks 1.5 wks 2 wks 3 wks 5.5 wks 1.5 2 2.5 2 wks 2 2 2 wks 1.5 1.5 wks wks wks wks wks wks wks Assurances for a Guaranteed and Viable Curriculum Adherence to this scope and sequence affords every member of the learning community clarity on the knowledge and skills on which each learner should demonstrate proficiency. In order to deliver a guaranteed and viable curriculum, our team commits to and ensures the following understandings: Shared Accountability: Responding -
Chapter 9 Titrimetric Methods 413
Chapter 9 Titrimetric Methods Chapter Overview Section 9A Overview of Titrimetry Section 9B Acid–Base Titrations Section 9C Complexation Titrations Section 9D Redox Titrations Section 9E Precipitation Titrations Section 9F Key Terms Section 9G Chapter Summary Section 9H Problems Section 9I Solutions to Practice Exercises Titrimetry, in which volume serves as the analytical signal, made its first appearance as an analytical method in the early eighteenth century. Titrimetric methods were not well received by the analytical chemists of that era because they could not duplicate the accuracy and precision of a gravimetric analysis. Not surprisingly, few standard texts from the 1700s and 1800s include titrimetric methods of analysis. Precipitation gravimetry developed as an analytical method without a general theory of precipitation. An empirical relationship between a precipitate’s mass and the mass of analyte— what analytical chemists call a gravimetric factor—was determined experimentally by taking a known mass of analyte through the procedure. Today, we recognize this as an early example of an external standardization. Gravimetric factors were not calculated using the stoichiometry of a precipitation reaction because chemical formulas and atomic weights were not yet available! Unlike gravimetry, the development and acceptance of titrimetry required a deeper understanding of stoichiometry, of thermodynamics, and of chemical equilibria. By the 1900s, the accuracy and precision of titrimetric methods were comparable to that of gravimetric methods, establishing titrimetry as an accepted analytical technique. 411 412 Analytical Chemistry 2.0 9A Overview of Titrimetry We are deliberately avoiding the term In titrimetry we add a reagent, called the titrant, to a solution contain- analyte at this point in our introduction ing another reagent, called the titrand, and allow them to react. -
Calorimetry the Science of Measuring Heat Generated Or Consumed During a Chemical Reaction Or Phase Change
February 05, 2014 Calorimetry the science of measuring heat generated or consumed during a chemical reaction or phase change What is going to happen when the burner is lit? February 05, 2014 Experimental Design Chemical changes involve potential energy, which cannot be measured directly Chemical reactions absorb or release energy with the surroundings, which cause a change in temperature of the surroundings (and this can be measured) In a calorimetry experiment, we set up the experiment so all of the energy from the reaction (the system) is exchanged with the surroundings ∆Esystem = ∆Esurroundings Chemical System Surroundings (water) Endothermic Change February 05, 2014 Chemical System Surroundings (water) Exothermic Change ∆Esystem = ∆Esurroundings February 05, 2014 There are three main calorimeter designs: 1) Flame calorimeter -a fuel is burned below a metal container filled with water 2) Bomb Calorimeter -a reaction takes place inside an enclosed vessel with a surrounding sleeve filled with water 3) Simple Calorimeter -a reaction takes place in a polystyrene cup filled with water Example #1 A student assembles a flame calorimeter by putting 350 grams of water into a 15.0 g aluminum can. A burner containing ethanol is lit, and as the ethanol is burning the temperature of the water increases by 6.30 ˚C and the mass of the ethanol burner decreases by 0.35 grams. Use this information to calculate the molar enthalpy of combustion of ethanol. February 05, 2014 The following apparatus can be used to determine the molar enthalpy of combustion of butan-2-ol. Initial mass of the burner: 223.50 g Final mass of the burner : 221.25 g water Mass of copper can + water: 230.45 g Mass of copper can : 45.60 g Final temperature of water: 67.0˚C Intial temperature of water : 41.3˚C Determine the molar enthalpy of combustion of butan-2-ol. -
Analytical Chemistry Laboratory Manual 2
ANALYTICAL CHEMISTRY LABORATORY MANUAL 2 Ankara University Faculty of Pharmacy Department of Analytical Chemistry Analytical Chemistry Practices Contents INTRODUCTION TO QUANTITATIVE ANALYSIS ......................................................................... 2 VOLUMETRIC ANALYSIS .............................................................................................................. 2 Volumetric Analysis Calculations ................................................................................................... 3 Dilution Factor ................................................................................................................................ 4 Standard Solutions ........................................................................................................................... 5 Primary standard .............................................................................................................................. 5 Characteristics of Quantitative Reaction ......................................................................................... 5 Preparation of 1 L 0.1 M HCl Solution ........................................................................................... 6 Preparation of 1 L 0.1 M NaOH Solution ....................................................................................... 6 NEUTRALIZATION TITRATIONS ...................................................................................................... 7 STANDARDIZATION OF 0.1 N NaOH SOLUTION ...................................................................... -
Biological Multi-Functionalization and Surface Nanopatterning of Biomaterials Zhe Annie Cheng
Biological multi-functionalization and surface nanopatterning of biomaterials Zhe Annie Cheng To cite this version: Zhe Annie Cheng. Biological multi-functionalization and surface nanopatterning of biomaterials. Other. Université Sciences et Technologies - Bordeaux I; Université catholique de Louvain (1970- ..), 2013. English. NNT : 2013BOR15202. tel-01016695 HAL Id: tel-01016695 https://tel.archives-ouvertes.fr/tel-01016695 Submitted on 1 Jul 2014 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. THÈSE PRÉSENTÉE A L’UNIVERSITÉ BORDEAUX 1 ÉCOLE DOCTORALE DES SCIENCES CHIMIQUES Par Zhe (Annie) CHENG POUR OBTENIR LE GRADE DE DOCTEUR SPÉCIALITÉ : POLYMÈRES Biological Multi-Functionalization and Surface Nanopatterning of Biomaterials Directeurs de thèse : Mme. Marie-Christine DURRIEU & M. Alain M. JONAS Soutenue le : 10 décembre, 2013 Devant la commission d’examen formée de : Mme. MIGONNEY, Véronique Professeur de l’Université Paris 13, France Rapporteur Mme. PICART, Catherine Professeur de l’Université Grenoble INP, France Rapporteur M. GAIGNEAUX, Eric Professeur de l’Université catholique de Louvain, Belgique Examinateur M. AYELA, Cédric Chargé de Recherche CNRS, Bordeaux, France Examinateur Mme. FOULC, Marie-Pierre Ingénieur de Recherche, Rescoll, Bordeaux, France Examinateur Mme. GLINEL, Karine Professeur de l’Université catholique de Louvain, Belgique Examinateur M. -
Page 1 of 4 Chemcomm
ChemComm Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/chemcomm Page 1 of 4 ChemComm Chemical Communications RSC Publishing COMMUNICATION Multi-responsive ionic liquid emulsions stabilized by microgels. Cite this: DOI: 10.1039/x0xx00000x Hélène Monteillet,a Marcel Workamp, a Xiaohua Li, b Boelo Schuur, b J. Mieke a a a Kleijn, Frans A.M. Leermakers, and Joris Sprakel* Received 00th January 2012, Accepted 00th January 2012 DOI: 10.1039/x0xx00000x www.rsc.org/ We present a complete toolbox to use responsive ionic liquid provide excellent stability to a wide variety of IL-water emulsions. (IL) emulsions for extraction purposes. IL emulsions The spontaneously formed and densely packed layer of microgels at the IL-water interface does not impart their use in extractions as the stabilized by responsive microgels are shown to allow rapid Manuscript interface remains permeable to small biomolecules. -
Chapter 8: Gravimetric Methods
Chapter 8 Gravimetric Methods Chapter Overview 8A Overview of Gravimetric Methods 8B Precipitation Gravimetry 8C Volatilization Gravimetry 8D Particulate Gravimetry 8E Key Terms 8F Chapter Summary 8G Problems 8H Solutions to Practice Exercises Gravimetry includes all analytical methods in which the analytical signal is a measurement of mass or a change in mass. When you step on a scale after exercising you are making, in a sense, a gravimetric determination of your mass. Mass is the most fundamental of all analytical measurements, and gravimetry is unquestionably our oldest quantitative analytical technique. The publication in 1540 of Vannoccio Biringuccio’sPirotechnia is an early example of applying gravimetry—although not yet known by this name—to the analysis of metals and ores.1 Although gravimetry no longer is the most important analytical method, it continues to find use in specialized applications. 1 Smith, C. S.; Gnodi, M. T. translation of Biringuccio, V. Pirotechnia, MIT Press: Cambridge, MA, 1959. 355 356 Analytical Chemistry 2.0 8A Overview of Gravimetric Methods Before we consider specific gravimetric methods, let’s take a moment to develop a broad survey of gravimetry. Later, as you read through the de- scriptions of specific gravimetric methods, this survey will help you focus on their similarities instead of their differences. You will find that it is easier to understand a new analytical method when you can see its relationship to other similar methods. 8A.1 Using Mass as an Analytical Signal Method 2540D in Standard Methods for Suppose you are to determine the total suspended solids in the water re- the Examination of Waters and Wastewaters, leased by a sewage-treatment facility. -
Basic Keyword List
NOTICE TO AUTHORS 2008 Basic Keyword list A Antibodies Bismuth Chalcogens Ab initio calculations Antifungal agents Block copolymers Chaperone proteins Absorption Antigens Bond energy Charge carrier injection Acidity Antimony Bond theory Charge transfer Actinides Antisense agents Boranes Chelates Acylation Antitumor agents Borates Chemical vapor deposition Addition to alkenes Antiviral agents Boron Chemical vapor transport Addition to carbonyl com- Aqueous-phase catalysis Bridging ligands Chemisorption pounds Arene ligands Bromine Chemoenzymatic synthesis Adsorption Arenes Brønsted acids Chemoselectivity Aerobic oxidation Argon Chiral auxiliaries Aggregation Aromatic substitution C Chiral pool Agostic interactions Aromaticity C-C activation Chiral resolution Alanes Arsenic C-C bond formation Chirality Alcohols Arylation C-C coupling Chlorine Aldehydes Aryl halides C-Cl bond activation Chromates Aldol reaction Arynes C-Glycosides Chromium Alkali metals As ligands C-H activation Chromophores Alkaline earth metals Asymmetric amplification C1 building blocks Circular dichroism Alkaloids Asymmetric catalysis Cadmium Clathrates Alkanes Asymmetric synthesis Cage compounds Clays Alkene ligands Atmospheric chemistry Calcium Cleavage reactions Alkenes Atom economy Calixarenes Cluster compounds Alkylation Atropisomerism Calorimetry Cobalamines Alkyne ligands Aurophilicity Carbanions Cobalt Alkynes Autocatalysis Carbene homologues Cofactors Alkynylation Automerization Carbene ligands Colloids Allenes Autoxidation Carbenes Combinatorial chemistry Allosterism -
Photochemistry of Highly Excited States R
COMMENTARY COMMENTARY Photochemistry of highly excited states R. D. Levinea,b,c,1 These days on earth we are photochemically reasonably A forceful illustration of the benefits of the synergy of well shielded. The far UV radiation is filtered by the ozone experiment and theory in understanding the detailed and other components of the atmosphere. In the iono- electronic and nuclear dynamics in highly excited states is sphere and beyond there is much challenging chemistry provided by the very recent work reported by Peters et al. induced by such higher-energy photons. The shielding by (8). Methyl azide is pumped by an 8-eV vacuum UV (VUV) the atmosphere also makes demands on such experi- pulse of 10-fs duration and probed by a second 1.6-eV in- ments in the laboratory. There is, however, recent interest frared (IR) pulse that ionizes the molecule. The experiment largely driven by technology that makes higher resolution as seen through the eyes of a theorist is shown in Fig. 1. The possible. The experimental technology is advanced light pump pulse prepares a single excited electronic state, la- sources that offer far higher intensities, sharper wave- beled as S8, that theory shows has a mixed valence and length definition or, complementarily, short-duration Rydberg character. It is unusual that a single excited state pulses. The two alternatives make a whole because of is accessed at such a high energy. The high-level computa- the quantum mechanical time–energy uncertainty princi- tions reported by Peters et al. are quite clear that the ple that makes short pulses necessarily broad in energy. -
Gravimetric Analysis
Gravimetric Analysis Gravimetric Analysis can be used to determine the percent composition of a species in a compound. This is known as quantitative analysis. An agent (precipitating agent) is chosen which will cause the species of interest to precipitate out of solution. The precipitate is then isolated and weighed. Through a series of calculations, the amount of the species in the original sample or compound can then be determined. 1. Weigh accurately about 0.5 g of the unknown, and dissolve it in water. The volume of water is not important, but you do want to make sure the solid is completely dissolved. 2. Add the precipitating agent in the form of solution. For example, to precipitate a chloride use a soluble salt of silver (AgNO3). 3. Add the precipitating agent until no more solid seems to precipitate. Allow the mixture to sit for about 5 minutes, and then add a few drops more, observing to see if any more precipitation occurs. If you see more solid forming, keep repeating the steps until no more precipitate results. Now separate the solid from the liquid. The mixture can be filtered by vacuum filtration through a weighed filter paper. Other methods involve gravity filtration or use of a centrifuge. Allow the solid to dry until you get a constant weight for readings at subsequent times (at least overnight or through use of an oven). 4. From the mass of precipitated compound (ppt) and the formula (in this case AgCl), you can calculate the percent composition of a species (in this case Cl-) in the original sample. -
Hectorite: Synthesis, Modification, Assembly and Applications Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang
Hectorite: Synthesis, modification, assembly and applications Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang To cite this version: Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang. Hectorite: Synthesis, modification, assembly and applications. Applied Clay Science, Elsevier, 2019, 177, pp.114-138. 10.1016/j.clay.2019.05.001. hal-02363196 HAL Id: hal-02363196 https://hal-cnrs.archives-ouvertes.fr/hal-02363196 Submitted on 2 Dec 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 Hectorite:Synthesis, Modification, Assembly and Applications 2 3 Jing Zhanga, Chun Hui Zhoua,b,c*, Sabine Petitd, Hao Zhanga 4 5 a Research Group for Advanced Materials & Sustainable Catalysis (AMSC), State Key Laboratory 6 Breeding Base of Green Chemistry-Synthesis Technology, College of Chemical Engineering, Zhejiang 7 University of Technology, Hangzhou 310032, China 8 b Key Laboratory of Clay Minerals of Ministry of Land and Resources of the People's Republic of 9 China, Engineering Research Center of Non-metallic Minerals of Zhejiang Province, Zhejiang Institute 10 of Geology and Mineral Resource, Hangzhou 310007, China 11 c Qing Yang Institute for Industrial Minerals, You Hua, Qing Yang, Chi Zhou 242804, China 12 d Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), UMR 7285 CNRS, Université de 13 Poitiers, Poitiers Cedex 9, France 14 15 Correspondence to: Prof. -
Carbon Nanostructures – from Molecules to Functionalised Materials
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 1537 Carbon Nanostructures – from Molecules to Functionalised Materials Fullerene-Ferrocene Oligomers, Graphene Modification and Deposition MICHAEL NORDLUND ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6214 ISBN 978-91-513-0019-1 UPPSALA urn:nbn:se:uu:diva-327189 2017 Dissertation presented at Uppsala University to be publicly examined in A1:107a, BMC, Husargatan 3, Uppsala, Friday, 22 September 2017 at 09:15 for the degree of Doctor of Philosophy. The examination will be conducted in English. Faculty examiner: Professor Mogens Brøndsted Nielsen (Copenhagen University, Department of chemistry). Abstract Nordlund, M. 2017. Carbon Nanostructures – from Molecules to Functionalised Materials. Fullerene-Ferrocene Oligomers, Graphene Modification and Deposition. Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 1537. 64 pp. Uppsala: Acta Universitatis Upsaliensis. ISBN 978-91-513-0019-1. The work described in this thesis concerns development, synthesis and characterisation of new molecular compounds and materials based on the carbon allotropes fullerene (C60) and graphene. A stepwise strategy to a symmetric ferrocene-linked dumbbell of fulleropyrrolidines was developed. The versatility of this approach was demonstrated in the synthesis of a non- symmetric fulleropyrrolidine-ferrocene-tryptophan triad. A new tethered bis-aldehyde, capable of regiospecific bis-pyrrolidination of a C60-fullerene in predominantly trans fashion, was designed, synthesised and reacted with glycine and C60 to yield the desired N-unfunctionalised bis(pyrrolidine)fullerene. A catenane dimer composed of two bis(pyrrolidine)fullerenes was obtained as a minor co-product. From the synthesis of the N-methyl analogue, the catenane dimer could be separated from the monomeric main product and fully characterised by NMR spectroscopy.