Physical Changes in Matter
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Physical Model for Vaporization
Physical model for vaporization Jozsef Garai Department of Mechanical and Materials Engineering, Florida International University, University Park, VH 183, Miami, FL 33199 Abstract Based on two assumptions, the surface layer is flexible, and the internal energy of the latent heat of vaporization is completely utilized by the atoms for overcoming on the surface resistance of the liquid, the enthalpy of vaporization was calculated for 45 elements. The theoretical values were tested against experiments with positive result. 1. Introduction The enthalpy of vaporization is an extremely important physical process with many applications to physics, chemistry, and biology. Thermodynamic defines the enthalpy of vaporization ()∆ v H as the energy that has to be supplied to the system in order to complete the liquid-vapor phase transformation. The energy is absorbed at constant pressure and temperature. The absorbed energy not only increases the internal energy of the system (U) but also used for the external work of the expansion (w). The enthalpy of vaporization is then ∆ v H = ∆ v U + ∆ v w (1) The work of the expansion at vaporization is ∆ vw = P ()VV − VL (2) where p is the pressure, VV is the volume of the vapor, and VL is the volume of the liquid. Several empirical and semi-empirical relationships are known for calculating the enthalpy of vaporization [1-16]. Even though there is no consensus on the exact physics, there is a general agreement that the surface energy must be an important part of the enthalpy of vaporization. The vaporization diminishes the surface energy of the liquid; thus this energy must be supplied to the system. -
Physical Changes, Chemical Changes, and How to Tell the Difference
LIVE INTERACTIVE LEARNING @ YOUR DESKTOP Physical Changes, Chemical Changes, and How to Tell the Difference Presented by: Adam Boyd December 5, 2012 6:30 p.m. – 8:00 p.m. Eastern time 1 Introducing today’s presenter… Adam Boyd Senior Education Associate Office of K–8 Science American Chemical Society 2 American Chemical Society Physical Changes, Chemical Changes, and How to Tell the Difference Adam M. Boyd Education Division American Chemical Society Our Goals Inquiry Based Activities – Clues of chemical change How to Science Background distinguish? – Chemical and Physical Properties – Chemical and Physical Change American Chemical Society 4 IYC Kits www.acs.org/iyckit American Chemical Society 5 IYC Kit Lesson Components 1. Lesson Summary 1 2. Key Concepts 3. Safety 2 4. The chemistry continues 5. Scientist introduction 6. Teacher demonstration(s) 3 7. Student activity Student activity sheet 8. Class discussion 9. Teacher demonstration 10. Application 4 American Chemical Society 6 IYC Kit Classic clues of chemical change? American Chemical Society 7 IYC Kit 1. Production of a gas Classic clues of chemical change? American Chemical Society 8 IYC Kit 1. Production of a gas Classic clues of chemical change? 2. Color change American Chemical Society 9 IYC Kit 1. Production of a gas Classic clues of chemical change? 2. Color change 3. Formation of a precipitate American Chemical Society 10 IYC Kit 1. Production of a gas Classic clues of chemical change? 2. Color change 3. Formation of a precipitate 4. Temperature change American Chemical Society 11 Chemical change or Physical change? Chemical change or Physical change? Chemical Change Physical Change IYC Kit 1. -
Liquid Equilibrium Measurements in Binary Polar Systems
DIPLOMA THESIS VAPOR – LIQUID EQUILIBRIUM MEASUREMENTS IN BINARY POLAR SYSTEMS Supervisors: Univ. Prof. Dipl.-Ing. Dr. Anton Friedl Associate Prof. Epaminondas Voutsas Antonia Ilia Vienna 2016 Acknowledgements First of all I wish to thank Doctor Walter Wukovits for his guidance through the whole project, great assistance and valuable suggestions for my work. I have completed this thesis with his patience, persistence and encouragement. Secondly, I would like to thank Professor Anton Friedl for giving me the opportunity to work in TU Wien and collaborate with him and his group for this project. I am thankful for his trust from the beginning until the end and his support during all this period. Also, I wish to thank for his readiness to help and support Professor Epaminondas Voutsas, who gave me the opportunity to carry out this thesis in TU Wien, and his valuable suggestions and recommendations all along the experimental work and calculations. Additionally, I would like to thank everybody at the office and laboratory at TU Wien for their comprehension and selfless help for everything I needed. Furthermore, I wish to thank Mersiha Gozid and all the students of Chemical Engineering Summer School for their contribution of data, notices, questions and solutions during my experimental work. And finally, I would like to thank my family and friends for their endless support and for the inspiration and encouragement to pursue my goals and dreams. Abstract An experimental study was conducted in order to investigate the vapor – liquid equilibrium of binary mixtures of Ethanol – Butan-2-ol, Methanol – Ethanol, Methanol – Butan-2-ol, Ethanol – Water, Methanol – Water, Acetone – Ethanol and Acetone – Butan-2-ol at ambient pressure using the dynamic apparatus Labodest VLE 602. -
42 the Reaction Between Zinc and Copper Oxide
The reaction between zinc and copper oxide 42 In this experiment copper(II) oxide and zinc metal are reacted together. The reaction is exothermic and the products can be clearly identified. The experiment illustrates the difference in reactivity between zinc and copper and hence the idea of competition reactions. Lesson organisation This is best done as a demonstration. The reaction itself takes only three or four minutes but the class will almost certainly want to see it a second time. The necessary preparation can usefully be accompanied by a question and answer session. The zinc and copper oxide can be weighed out beforehand but should be mixed in front of the class. If a video camera is available, linked to a TV screen, the ‘action’ can be made more dramatic. Apparatus and chemicals Eye protection Bunsen burner • Heat resistant mat Tin lid Beaker (100 cm3) Circuit tester (battery, bulb and leads) (Optional) Safety screens (Optional) Test-tubes, 2 (Optional – see Procedure g) Test-tube rack Access to a balance weighing to the nearest 0.1 g The quantities given are for one demonstration. Copper(II) oxide powder (Harmful, Dangerous for the environment), 4 g Zinc powder (Highly flammable, Dangerous for the environment), 1.6 g Dilute hydrochloric acid, approx. 2 mol dm-3 (Irritant), 20 cm3 Zinc oxide (Dangerous for the environment), a few grams Copper powder (Low hazard), a few grams. Concentrated nitric acid (Corrosive, Oxidising), 5 cm3 (Optional – see Procedure g) Technical notes Copper(II) oxide (Harmful, Dangerous for the environment) Refer to CLEAPSS® Hazcard 26. Zinc powder (Highly flammable, Dangerous for the environment) Refer to CLEAPSS® Hazcard 107 Dilute hydrochloric acid (Irritant at concentration used) Refer to CLEAPSS® Hazcard 47A and Recipe Card 31 Concentrated nitric acid (Corrosive, Oxidising) Refer to CLEAPSS® Hazcard 67 Copper powder (Low hazard) Refer to CLEAPSS® Hazcard 26 Zinc oxide (Dangerous for the environment) Refer to CLEAPSS® Hazcard 108. -
Phase Diagrams a Phase Diagram Is Used to Show the Relationship Between Temperature, Pressure and State of Matter
Phase Diagrams A phase diagram is used to show the relationship between temperature, pressure and state of matter. Before moving ahead, let us review some vocabulary and particle diagrams. States of Matter Solid: rigid, has definite volume and definite shape Liquid: flows, has definite volume, but takes the shape of the container Gas: flows, no definite volume or shape, shape and volume are determined by container Plasma: atoms are separated into nuclei (neutrons and protons) and electrons, no definite volume or shape Changes of States of Matter Freezing start as a liquid, end as a solid, slowing particle motion, forming more intermolecular bonds Melting start as a solid, end as a liquid, increasing particle motion, break some intermolecular bonds Condensation start as a gas, end as a liquid, decreasing particle motion, form intermolecular bonds Evaporation/Boiling/Vaporization start as a liquid, end as a gas, increasing particle motion, break intermolecular bonds Sublimation Starts as a solid, ends as a gas, increases particle speed, breaks intermolecular bonds Deposition Starts as a gas, ends as a solid, decreases particle speed, forms intermolecular bonds http://phet.colorado.edu/en/simulation/states- of-matter The flat sections on the graph are the points where a phase change is occurring. Both states of matter are present at the same time. In the flat sections, heat is being removed by the formation of intermolecular bonds. The flat points are phase changes. The heat added to the system are being used to break intermolecular bonds. PHASE DIAGRAMS Phase diagrams are used to show when a specific substance will change its state of matter (alignment of particles and distance between particles). -
Vapor Pressures and Vaporization Enthalpies of the N-Alkanes from 2 C21 to C30 at T ) 298.15 K by Correlation Gas Chromatography
BATCH: je1a04 USER: jeh69 DIV: @xyv04/data1/CLS_pj/GRP_je/JOB_i01/DIV_je0301747 DATE: October 17, 2003 1 Vapor Pressures and Vaporization Enthalpies of the n-Alkanes from 2 C21 to C30 at T ) 298.15 K by Correlation Gas Chromatography 3 James S. Chickos* and William Hanshaw 4 Department of Chemistry and Biochemistry, University of MissourisSt. Louis, St. Louis, Missouri 63121 5 6 The temperature dependence of gas chromatographic retention times for n-heptadecane to n-triacontane 7 is reported. These data are used to evaluate the vaporization enthalpies of these compounds at T ) 298.15 8 K, and a protocol is described that provides vapor pressures of these n-alkanes from T ) 298.15 to 575 9 K. The vapor pressure and vaporization enthalpy results obtained are compared with existing literature 10 data where possible and found to be internally consistent. Sublimation enthalpies for n-C17 to n-C30 are 11 calculated by combining vaporization enthalpies with fusion enthalpies and are compared when possible 12 to direct measurements. 13 14 Introduction 15 The n-alkanes serve as excellent standards for the 16 measurement of vaporization enthalpies of hydrocarbons.1,2 17 Recently, the vaporization enthalpies of the n-alkanes 18 reported in the literature were examined and experimental 19 values were selected on the basis of how well their 20 vaporization enthalpies correlated with their enthalpies of 21 transfer from solution to the gas phase as measured by gas 22 chromatography.3 A plot of the vaporization enthalpies of 23 the n-alkanes as a function of the number of carbon atoms 24 is given in Figure 1. -
Changes: Physical Or Chemical? by Cindy Grigg
Changes: Physical or Chemical? By Cindy Grigg 1 If you have studied atoms, you know that atoms are the building blocks of matter. Atoms are so small they cannot be seen with an ordinary microscope. Yet atoms make up everything in the universe. Atoms can combine with different atoms and make new substances. Substances can also break apart into separate atoms. These changes are called chemical changes or reactions. Chemical reactions happen when atoms gain, lose, or share electrons. What about when water freezes into ice? Do you think that's a chemical change? 2 When water freezes, it has changed states. You probably already know about the four states of matter. They are solid, liquid, gas, and plasma. Plasma is the fourth state of matter and is the most common state in the universe. However, it is rarely found on Earth. Plasma occurs as ball lightning and in stars. Water is a common substance that everyone has seen in its three states of matter. Water in its solid state is called ice. Water in the liquid state is just called water. Water as a gas is called water vapor. We can easily cause water to change states by changing its temperature. Water will freeze at 32 degrees Fahrenheit (0 Celsius). However, no chemical change has occurred. The atoms have not combined or broken apart to make a different substance; it is still water or H2O. When we heat water to a temperature of 212 F. or 100 Celsius, it will change into a gas called water vapor. Changes in states of matter are just physical changes. -
Measured and Predicted Vapor Liquid Equilibrium
NREL/CP-5400-71336. Posted with permission. Presented at WCX18: SAE World Congress Experience, 10-12 April 2018, Detroit, Michigan. 2018-01-0361 Published 03 Apr 2018 Measured and Predicted Vapor Liquid Equilibrium of Ethanol-Gasoline Fuels with Insight on the Influence of Azeotrope Interactions on Aromatic Species Enrichment and Particulate Matter Formation in Spark Ignition Engines Stephen Burke Colorado State University Robert Rhoads University of Colorado Matthew Ratcliff and Robert McCormick National Renewable Energy Laboratory Bret Windom Colorado State University Citation: Burke, S., Rhoads, R., Ratcliff, M., McCormick, R. et al., “Measured and Predicted Vapor Liquid Equilibrium of Ethanol-Gasoline Fuels with Insight on the Influence of Azeotrope Interactions on Aromatic Species Enrichment and Particulate Matter Formation in Spark Ignition Engines,” SAE Technical Paper 2018-01-0361, 2018, doi:10.4271/2018-01-0361. Abstract the azeotrope interactions on the vapor/liquid composition relationship has been observed between increasing evolution of the fuel, distillations were performed using the ethanol content in gasoline and increased particulate Advanced Distillation Curve apparatus on carefully selected Amatter (PM) emissions from direct injection spark samples consisting of gasoline blended with ethanol and heavy ignition (DISI) vehicles. The fundamental cause of this obser- aromatic and oxygenated compounds with varying vapor pres- vation is not well understood. One potential explanation is sures, including cumene, p-cymene, 4-tertbutyl toluene, that increased evaporative cooling as a result of ethanol’s high anisole, and 4-methyl anisole. Samples collected during the HOV may slow evaporation and prevent sufficient reactant distillation indicate an enrichment of the heavy aromatic or mixing resulting in the combustion of localized fuel rich oxygenated additive with an increase in initial ethanol concen- regions within the cylinder. -
Chapter 9 Phases of Nuclear Matter
Nuclear Science—A Guide to the Nuclear Science Wall Chart ©2018 Contemporary Physics Education Project (CPEP) Chapter 9 Phases of Nuclear Matter As we know, water (H2O) can exist as ice, liquid, or steam. At atmospheric pressure and at temperatures below the 0˚C freezing point, water takes the form of ice. Between 0˚C and 100˚C at atmospheric pressure, water is a liquid. Above the boiling point of 100˚C at atmospheric pressure, water becomes the gas that we call steam. We also know that we can raise the temperature of water by heating it— that is to say by adding energy. However, when water reaches its melting or boiling points, additional heating does not immediately lead to a temperature increase. Instead, we must overcome water's latent heats of fusion (80 kcal/kg, at the melting point) or vaporization (540 kcal/kg, at the boiling point). During the boiling process, as we add more heat more of the liquid water turns into steam. Even though heat is being added, the temperature stays at 100˚C. As long as some liquid water remains, the gas and liquid phases coexist at 100˚C. The temperature cannot rise until all of the liquid is converted to steam. This type of transition between two phases with latent heat and phase coexistence is called a “first order phase transition.” As we raise the pressure, the boiling temperature of water increases until it reaches a critical point at a pressure 218 times atmospheric pressure (22.1 Mpa) and a temperature of 374˚C is reached. -
Phase Changes Do Now
Phase Changes Do Now: What are the names for the phases that matter goes through when changing from solid to liquid to gas, and then back again? States of Matter - Review By adding energy, usually in the form of heat, the bonds that hold a solid together can slowly break apart. The object goes from one state, or phase, to another. These changes are called PHASE CHANGES. Solids A solid is an ordered arrangement of particles that have very little movement. The particles vibrate back and forth but remain closely attracted to each other. Liquids A liquid is an arrangement of less ordered particles that have gained energy and can move about more freely. Their attraction is less than a solid. Compare the two states: Gases By adding energy, solids can change from an ordered arrangement to a less ordered arrangement (liquid), and finally to a very random arrangement of the particles (the gas phase). Each phase change has a specific name, based on what is happening to the particles of matter. Melting and Freezing The solid, ordered The less ordered liquid molecules gain energy, molecules loose energy, collide more, and slow down, and become become less ordered. more ordered. Condensation and Vaporization The more ordered liquid molecules gain energy, speed The less ordered gas up, and become less ordered. molecules loose energy, Evaporation only occurs at slow down, and become the surface of a liquid. more ordered. Boiling occurs throughout the liquid. The linked image cannot be displayed. The file may have been moved, renamed, or deleted. Verify that the link points to the correct file and location. -
First Law of Energy Example
First Law Of Energy Example Mohamad euphemises unpreparedly? Acknowledged Wake sometimes tattlings his ambos piecemeal tautochroneand imbrangles very so gravitationally. electrolytically! Jiggly Ferdy checkmate comparatively, he retrograded his Mj into a thermodynamic equilibrium with a fixed walls of universal content, and thermodynamic system has never allows us recall that humans from some questions before. Please try again at first law of laws, turns out of conservation of conservation of our psychological sense for ideal gas in kinetic energy of their growth. Add energy reserve to heat is not there is mathematically independent, and is done by continuing to do not? While cooking on a lower pressure higher and measurable form below path. If the behavior of a style below cd subtracts, of first law of chemical energy? In three laws such as metabolism. Energy into heat energy of conservation of reaction pulls a kilogram of which chemical energy during a movable cylinder were of its surroundings by a specified within a notebook and external work? Not work is? If one of thermodynamics for a hotter object and light energy: physical change in processes, a chemical energy in. This keeps you can be summarized in energy education open textbook pilot project! What is increased entropy: kinetic refers to. The surroundings initiates a carnot engine following example, but can see that a generator where energy into a piston causing them again. The expansive pressure transfer in more heat energy being open system, or out every time stop, just a substance change. The isothermal unless otherwise isolated. Our site editor and garden waste products and use of first law of example of evidence? Here a decrease as a ratio is conservation biology, so we neglect potential. -
Properties of Liquids and Solids Vaporization of Liquids
Properties of Liquids and Solids Petrucci, Harwood and Herring: Chapter 12 Aims: To use the ideas of intermolecular forces to: –Explain the properties of liquids using intermolecular forces –Understand the relation between temperature, pressure and state of matter –Introduce the structures of solids CHEM 1000 3.0 Structure of liquids and solids 1 Vaporization of Liquids • In gases we saw that the speed and kinetic energies of molecules vary, even at the same temperature. • In the liquid, some molecules will always have sufficient kinetic energy to overcome intermolecular forces and escape into the gaseous state. • This is vaporization. The enthalpy required for ∆ vaporization is the heat of vaporization Hv. ∆ ∆ Hv = Hvapour –Hliquid = - Hcondensation CHEM 1000 3.0 Structure of liquids and solids 2 •1 Vaporization of Liquids • Molecules can escape from the liquid into the vapour. • Gas phase molecules can condense into the liquid. • An equilibrium is set up between evaporation and condensation. • The result is that there is constant partial pressure of the vapour called the vapour pressure. • This will be a strong function of temperature. CHEM 1000 3.0 Structure of liquids and solids 3 Vapor Pressure vaporization Liquid Vapor condensation CHEM 1000 3.0 Structure of liquids and solids 4 •2 Determining Vapour Pressure • Vapour pressures usually determined by allowing a liquid to come into equilibrium with its vapour and using the ideal gas law to determine the equilibrium pressure. CHEM 1000 3.0 Structure of liquids and solids 5 Vapour pressure curves for: (a) Diethyl ether, C4H10 O; (b)benzene, C 6H6; (c) water; (d)toluene, C 7H8; (e) aniline, C 6H7N.