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Becky Kriger

What are Ziegler-Natta Catalysts? - 0 views

  • It was discovered that Group IV metals, especially titanium, were effective polymerization catalysts for ethylene. Following Ziegler’s successful preparation of linear polyethylene in 1953, Giulio Natta prepared and isolated isotactic (crystalline) polypropylene at the Milan Polytechnic Institute. This was immediately recognized for its practical importance. Ziegler and Natta shared the Nobel Prize in Chemistry in 1963.
  • A Ziegler-Natta catalyst is composed of at least two parts: a transition metal component and a main group metal alkyl compound. The transition metal component is usually either titanium or vanadium. The main group metal alkyl compound is usually an aluminum alkyl. In common practice, the titanium component is called "the catalyst’ and the aluminum alkyl is called "the co-catalyst".
  • In some instances, especially for catalyzing the polymerization of propylene, a third component is used. This component is used to control stereoregularity
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  • Today, Ziegler-Natta catalysts are used worldwide to produce the following classes of polymers from alpha olefins: High density polyethylene (HDPE) Linear low density polyethylene (LLDPE) Ultra-high molecular weight polyethylene (UHMWPE) Polypropylene (PP)--homopolymer, random copolymer and high impact copolymers Thermoplastic polyolefins (TPO’s) Ethylene propylene diene monomer polymers (EPDM) Polybutene (PB)
Becky Kriger

Addition Polymers - 0 views

  • Addition polymers are usually made from molecules that have the following general structure: Different W, X, Y, and Z groups distinguish one addition polymer from another.
  • In the first stage, a substance is split into two identical parts, each with an unpaired electron. (Peroxides, which contain an O-O bond, are often used in this role.) A molecule with an unpaired electron is called a free radical. The free radical then initiates the reaction sequence by forming a bond to one of the carbon atoms in the double bond of the monomer. One electron for this new bond comes from the free radical, and the second electron for the new bond comes from one of the two bonds between the carbon atoms. The remaining electron from the broken bond shifts to the carbon atom on the far side of the molecule, away from the newly formed bond, forming a new free radical. Each half-headed arrow indicates the shift of one electron.
  • The chain begins to grow--propagate, stage two--when the new free radical formed in the initiation stage reacts with another monomer to add two more carbon atoms. This process repeats over and over again
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  • It can be terminated--stage three--when any two free radicals combine, thus pairing their unpaired electrons and forming a covalent bond that links two chains together.
  • Polyethylene molecules made with the free radical initiation process tend to form branches that keep the molecules from fitting closely together. Techniques have been developed that use catalysts, like Cr2O3, to make polyethylene molecules with very few branches.
  • yielding a high-density polyethylene, HDPE, that is more opaque, harder, and stronger than the low-density polyethylene, LDPE, made with free radical initiation.
Becky Kriger

Introduction to DNA Structure - 0 views

  • Pyrimidine Bases Cytosine and thymine are pyrimidines. The 6 stoms (4 carbon, 2 nitrogen) are numbered 1-6. Like purines, all pyrimidine ring atoms lie in the same plane. Structure of C and T
  • DNA is a polymer. The monomer units of DNA are nucleotides, and the polymer is known as a "polynucleotide." Each nucleotide consists of a 5-carbon sugar (deoxyribose), a nitrogen containing base attached to the sugar, and a phosphate group. There are four different types of nucleotides found in DNA, differing only in the nitrogenous base.
  • Adenine and guanine are purines. Purines are the larger of the two types of bases found in DNA. Structures are shown below: Structure of A and G
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  • The 9 atoms that make up the fused rings (5 carbon, 4 nitrogen) are numbered 1-9. All ring atoms lie in the same plane.
  • The deoxyribose sugar of the DNA backbone has 5 carbons and 3 oxygens. The carbon atoms are numbered 1', 2', 3', 4', and 5' to distinguish from the numbering of the atoms of the purine and pyrmidine rings. The hydroxyl groups on the 5'- and 3'- carbons link to the phosphate groups to form the DNA backbone
  • A nucleoside is one of the four DNA bases covalently attached to the C1' position of a sugar.
  • Nucleosides differ from nucleotides in that they lack phosphate groups. The four different nucleosides of DNA are deoxyadenosine (dA), deoxyguanosine (dG), deoxycytosine (dC), and (deoxy)thymidine (dT, or T).
  • A nucleotide is a nucleoside with one or more phosphate groups covalently attached to the 3'- and/or 5'-hydroxyl group(s).
  • The DNA backbone is a polymer with an alternating sugar-phosphate sequence. The deoxyribose sugars are joined at both the 3'-hydroxyl and 5'-hydroxyl groups to phosphate groups in ester links, also known as "phosphodiester" bonds.
  • DNA is a normally double stranded macromolecule. Two polynucleotide chains, held together by weak thermodynamic forces, form a DNA molecule.
  • Two DNA strands form a helical spiral, winding around a helix axis in a right-handed spiral The two polynucleotide chains run in opposite directions The sugar-phosphate backbones of the two DNA strands wind around the helix axis like the railing of a sprial staircase The bases of the individual nucleotides are on the inside of the helix, stacked on top of each other like the steps of a spiral staircase.
  • Within the DNA double helix, A forms 2 hydrogen bonds with T on the opposite strand, and G forms 3 hyrdorgen bonds with C on the opposite strand.
Justin Shorb

Chemistry: The Molecular Science - Google Book Search - 0 views

  • Chemistry : the molecular science
  • 8.8 Formal Charge
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    Helps to answer Exam I #4
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    Page in Moore et al. text about Unit cells.
Justin Shorb

Window on the Solid State - Unit Cell - 0 views

  • Note that the edges of these cells all connect lattice points in the structure, points with the same environments.
    • Justin Shorb
       
      Be sure that when you draw a unit cell, if you place the 'left' edge against the 'right' edge, they have the same lattice points touching!
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    Helpful for Exam I #3
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    Useful for understanding how Unit Cells work
Justin Shorb

Trends of the Periodic Table - 0 views

  • Atomic Radius
    • Justin Shorb
       
      For a, b (see below for ion size)
  • Electronegativity
    • Justin Shorb
       
      for (c)
  • Ionic Radius vs. Atomic Radius
    • Justin Shorb
       
      For (b)
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    • Justin Shorb
       
      Covalency has to do with how polar/non-polar the bond is. The more equal a partnership, the more covalent the bond is. Thus: compare electronegativities. Metal/non-metal pairs form ionic (extreme of polar covalent to the point of being NOT covalent) bonds.
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    Exam I, #1
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    Short exerpts on many basic Periodic Trends
Justin Shorb

Periodic Trends - Effective Nuclear Charge - 0 views

  • Slater's Rules
    • Justin Shorb
       
      Note that this is how you would calculate ENC - Although the nucleus gets MORE positive down the PT, the ENC actually decreases! Not just the compensation part, but actually in it's entirety.
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    A good short synopsis of ENC
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    Good for #8 Exam I
Justin Shorb

Prentice Hall Assets - Effective Nuclear Charge Video - 0 views

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    Good for Question #10
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    Video showing basic ENC concepts.
Justin Shorb

NSDL.org | Light Color Energy Educational Resources Search Results > Page 1 | The Nati... - 0 views

  • LIGHT: ITS SECRETS REVEALED
    • Justin Shorb
       
      This is a fairly large PDF file, but it has some good visual information!
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    Great PDF talking about light. Good images of how to go from wavelength to sizes of various objects.
John Moore

Diigo Annotation Tutorial - 0 views

    • John Moore
       
      Which is better? Presumably the tool bar is more powerful but the Diigolet is easier to use. Is that right?
    • Justin Shorb
       
      I think that the Digolet is actually easier, and doesn't require an install. The toolbar is more powerful, and the show/hide feature is nice. Try visiting this website to see where a show/hide feature would be nice: http://mashable.com/2006/07/24/diigo-launches-nobody-cares/
ChemPaths UW-Madison

Waves and Wave Motion - 0 views

    • A A
       
      Simple, direct tutorial on waves.
  • Waves can take many forms, but there are two fundamental types of waves: “longitudinal” and “transverse” (see Figures 1 and 2).
    • ChemPaths UW-Madison
       
      We didn't talk about this in class, but it helps explain why some waves can't even be seen moving - like longitudinal waves in the stones during earthquakes!
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    Excellent site on wave mechanics and the history of how we think about waves. Mostly about liquid waves.
Becky Kriger

The Science of Nylon - Spinning the Elements - 0 views

  • Nylon was developed as a synthetic substitute for silk.
  • Silk is a protein. Like all proteins, it is a polypeptide, and it has a structure something like this:
Justin Shorb

ChemPaths: Standing Waves: Chladni Plate - 0 views

  • It will produce a loud sound when a resonant frequency is reached.
    • Alex Schwartz
       
      Loud sound also produced by resonant frequencies...notice, resonant light waves produce visibly pleasing results while sound waves produce audibly noticable results.
    • Justin Shorb
       
      Yes, and resonate frequencies can produce non-pleasing results - the age old "shattering wine glass" which happens when an opera singer hits just the right 'resonating' high pitch!
Jongmin Lee

ChemPaths: Black Body Radiation - 0 views

    • Jongmin Lee
       
      Radiation It was discovered that normal objects actually emit radiation, or "glow". At room temperatures, this light that is emitted is usually not visible. But as has been seen on television, the use of night goggles permits the wearer to see infrared light. Warmer objects (like human bodies) appear to glow brighter. This is called black body radiation.
Michael Nonte

http://chemed.chem.wisc.edu/chempaths/paths/index.plx?path=waveTutorial&stone=3 - 0 views

    • Jongmin Lee
       
      As the wave frequency is increased, the wavelength decreases.
    • Justin Shorb
       
      Yes - what do you think this will end up meaning for relating color of light to energy of light? What does a long wavelength mean?
    • Michael Nonte
       
      1-D Vs. 2-D Waves
    • Justin Shorb
       
      Which of these waves was 1D and which 2D?
Jongmin Lee

ChemPaths: Standing Waves - 0 views

    • Jongmin Lee
       
      When a wave is confined to a specific place, only certain wavelengths--those that can fit the space available--are allowed. These allowed waves reflect from the boundaries of the space and the reflection reinforces the original wave (constructive interference). All other wavelengths cancel each other out by destructive interference.
    • ChemPaths UW-Madison
       
      Has anyone determined the pattern in the frequencies for the videos?
Michael Nonte

Mechanical Waves - 0 views

    • Michael Nonte
       
      On this page: -Propagation -Frequency -Wavelength
Justin Shorb

Quantum Mechanics: 2-Dimensional Rectangular Box Applet - 0 views

  • java applet
    • Justin Shorb
       
      Try selecting various energy levels at the top of the applet. We have only talked about being in a single energy level at a time - thus deselect an energy level before selecting another one.
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    Only look at this one if you loved problem #9
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    Really in depth look at Energy Levels, Wavefunctions, and superposition of wavefunctions.
Justin Shorb

Construct a Lewis Structure - 0 views

  • Starting with a structure indicating only atom connections
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    Useful for extra help in Lewis Diagrams.
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    Doesn't have the same molecules as Exam I #7, but is useful practice!
Justin Shorb

cramster.com | problem solved | q&a board questions - 0 views

  • Response Details:
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    Pictures of isomers for Exam I #5
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