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ChemPaths UW-Madison

Atomic Structure and Isotopes - 0 views

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    Hi!
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    Atomic and Ionic Radii | Boron Family | P-Block Elements | IIT-JEE NEET youtube.com/watch?v=fqK9e_jqKLU
ChemPaths UW-Madison

Electron Configurations - 6 views

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    This site is very helpful for problem 43.
Justin Shorb

Thermo-chemistry - 0 views

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    Does anyone understand why melting ice is endothermic?
Becky Kriger

Chemical of the Week -- Polymers - 0 views

  •  Polymers are substances whose molecules have high molar masses and are composed of a large number of repeating units. There are both naturally occurring and synthetic polymers. Among naturally occurring polymers are proteins, starches, cellulose, and latex. Synthetic polymers are produced commercially on a very large scale and have a wide range of properties and uses. The materials commonly called plastics are all synthetic polymers.
  •    Polymers are formed by chemical reactions in which a large number of molecules called monomers are joined sequentially, forming a chain.
  • If all atoms in the monomers are incorporated into the polymer, the polymer is called an addition polymer. If some of the atoms of the monomers are released into small molecules, such as water, the polymer is called a condensation polymer.
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  • Polyethylene terephthalate (PET), or polyethylene terephthalic ester (PETE), is a condensation polymer produced from the monomers ethylene glycol, HOCH2CH2OH, a dialcohol, and dimethyl terephthalate, CH3O2C–C6H4–CO2CH3, a diester. By the process of transesterification, these monomers form ester linkages between them, yielding a polyester
  • PETE fibers are manufactured under the trade names of Dacron and Fortrel.
  • Pleats and creases can be permanently heat set in fabrics containing polyester fibers, so-called permanent press fabrics. PETE can also be formed into transparent sheets and castings.
  • Transparent 2-liter carbonated beverage bottles are made from PETE.
  • ne form of PETE is the hardest known polymer and is used in eyeglass lenses.
  •      Polyethylene is perhaps the simplest polymer, composed of chains of repeating –CH2– units. It is produced by the addition polymerization of ethylene, CH2=CH2 (ethene)
  • HDPE is hard, tough, and resilient. Most HDPE is used in the manufacture of containers, such as milk bottles and laundry detergent jugs.
  • LDPE is relatively soft, and most of it is used in the production of plastic films, such as those used in sandwich bags.
  • Polymerization of vinyl chloride, CH2=CHCl (chloroethene), produces a polymer similar to polyethylene, but having chlorine atoms at alternate carbon atoms on the chain.
  • About two-thirds of the PVC produced annually is used in the manufacture of pipe. It is also used in the production of “vinyl” siding for houses and clear plastic bottles.
  • is used to form flexible articles such as raincoats and shower curtains.
  • This polymer is produced by the addition polymerization of propylene, CH2=CHCH3 (propene). Its molecular structure is similar to that of polyethylene, but has a methyl group (–CH3) on alternate carbon atoms of the chain.
  • olypropylene is used extensively in the automotive industry for interior trim, such as instrument panels, and in food packaging, such as yogurt containers. It is formed into fibers of very low absorbance and high stain resistance, used in clothing and home furnishings, especially carpeting.
  • Styrene, CH2=CH–C6H5, polymerizes readily to form polystyrene (PS), a hard, highly transparent polymer.
  • A large portion of production goes into packaging. The thin, rigid, transparent containers in which fresh foods, such as salads, are packaged are made from polystyrene. Polystyrene is readily foamed or formed into beads. These foams and beads are excellent thermal insulators and are used to produce home insulation and containers for hot foods. Styrofoam is a trade name for foamed polystyrene.
  • eflon is a trade name of polytetrafluoroethylene, PTFE. It is formed by the addition polymerization of tetrafluoroethylene, CF2=CF2 (tetrafluoroethene). PTFE is distinguished by its complete resistance to attack by virtually all chemicals and by its slippery surface. It maintains its physical properties over a large temperature range, -270° to 385°C. These properties make it especially useful for components that must operate under harsh chemical conditions and at temperature extremes. Its most familiar household use is as a coating on cooking utensils.
  • his important class of polymers is formed by the addition polymerization of an diisocyanate (whose molecules contain two –NCO groups) and a dialcohol (two –OH groups).
  • Polyurethane is spun into elastic fibers, called spandex, and sold under the trade name Lycra. Polyurethane can also be foamed. Soft polyurethane foams are used in upholstery, and hard foams are used structurally in light aircraft wings and sail boards.
  • Polyamides are a group of condensation polymers commonly known as nylon. Nylon is made from two monomers, one a dichloride and the other a diamine.
  • Nylon can be readily formed into fibers that are strong and long wearing, making them well suited for use in carpeting, upholstery fabric, tire cords, brushes, and turf for athletic fields. Nylon is also formed into rods, bars, and sheets that are easily formed and machined.
  • Polyacrylamide is a condensation polymer with an unusual and useful property.
  • This produces a network of polymer chains, rather like a tiny sponge. The free, unlinked amide groups, because they contain –NH2 groups, can form hydrogen bonds with water. This gives the tiny cross linked sponges a great affinity for water. Polyacrylamide can absorb many times its mass in water. T
  • his property is useful in a variety of applications, such as in diapers and in potting soil. The polyacrylamide will release the absorbed water if a substance that interferes with hydrogen bonding is added. Ionic substances, such as salt, cause polyacrylamide to release its absorbed water.
  • Over the past few decades, the use of polymers in disposable consumer goods has grown tremendously. This growth is proving to be taxing on the waste disposal system, consuming a large fraction of available landfill space.
  • To help sort wastes by type of polymer, most disposable polymeric goods are labeled with a recycling code: three arrows around a number above the polymer's acronym. These are intended to help consumers separate the waste polymers according to type before disposing of them. In the city of Madison, currently only type 1 (PETE) and type 2 (HDPE) polymers are being recycled – see below. The recycling of polymers is not a closed loop, where a material is reformed into new products repeatedly, such as in the case with aluminum. Most polymeric materials are recycled only once, and the product made of recycled polymer is discarded after use
  • General Rules Remove and discard all lids or caps. Rinse all containers. Remove and discard sprayer tops. CRUSH all plastic bottles to save space. No 5 gallon pails. No containers with metal handles.
  • What can be Recycled?Plastic Code Number Recyclable Containers Soda Bottles Water Bottles Juice Bottles Cooking Oil Bottles Soap/Detergent Bottles Shampoo Bottles Clear Liquor Bottles Food Jars (Peanut Butter etc.) Plastic Code Number Recyclable Containers Milk Bottles Water Bottles Juice Bottles Cooking Oil Containers Windshield Washer Fluid Bottles Shampoo Bottles Butter/Margarine Tubs Cottage Cheese Containers Ice Cream Containers Without Metal Handles Baby Wipe Containers Do NOT Recycle This Plastic 1. Automotive Product Containers Including: Motor Oil Bottles Anti-Freeze Containers Gasoline and Oil Additive Bottles 2. Brown Liquor Bottles 3. All Containers Marked With The Following Codes:            
Becky Kriger

Polymer - Condensation polymers - 1 views

  • Polymers are made up of extremely large, chainlike molecules consisting of numerous, smaller, repeating units called monomers. Polymer chains, which could be compared to paper clips linked together to make a long strand, appear in varying lengths. They can have branches, become intertwined, and can have cross-links. In addition, polymers can be composed of one or more types of monomer units, they can be joined by various kinds of chemical bonds, and they can be oriented in different ways. Monomers can be joined together by addition, in which all the atoms in the monomer are present in the polymer, or by condensation, in which a small molecule byproduct is also formed.
  • The importance of polymers is evident as they occur widely both in the natural world in such materials as wool, hair, silk and sand, and in the world of synthetic materials in nylon, rubber, plastics, Styrofoam, and many other materials.
  • Polymers are extremely large molecules composed of long chains, much like paper clips that are linked together to make a long strand. The individual subunits, which can range from as few as 50 to more than 20,000, are called monomers (from the Greek mono meaning one and meros meaning part). Because of their large size, polymers (from the Greek poly meaning many) are referred to as macromolecules.
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  • Most synthetic polymers are made from the non-renewable resource, petroleum, and as such, the "age of plastics" is limited unless other ways are found to make them. Since most polymers have carbon atoms as the basis of their structure, in theory at least, there are numerous materials that could be used as starting points.
  • Disposing of plastics is also a serious problem, both because they contribute to the growing mounds of garbage accumulating everyday and because most are not biodegradable. Researchers are busy trying to find ways to speed-up the decomposition time which, if left to occur naturally, can take decades.
  • n order for monomers to chemically combine with each other and form long chains, there must be a mechanism by which the individual units can join or bond to each other. One method by which this happens is called addition because no atoms are gained or lost in the process. The monomers simply "add" together and the polymer is called an addition polymer.
  • The simplest chemical structure by which this can happen involves monomers that contain double bonds (sharing two pairs of electrons). When the double bond breaks and changes into a single bond, each of the other two electrons are free and available to join with another monomer that has a free electron. This process can continue on and on. Polyethylene is an example of an addition polymer.
  • The polymerization process can be started by using heat and pressure or ultraviolet light or by using another more reactive chemical such as a peroxide. Under these conditions the double bond breaks leaving extremely reactive unpaired electrons called free radicals. These free radicals react readily with other free radicals or with double bonds and the polymer chain starts to form.
  • ifferent catalysts yield polymers with different properties because the size of the molecule may vary and the chains may be linear, branched, or cross-linked. Long linear chains of 10,000 or more monomers can pack very close together and form a hard, rigid, tough plastic known as high-density polyethylene or HDPE
  • Shorter, branched chains of about 500 monomers of ethylene cannot pack as closely together and this kind of polymer is known as low-density polyethylene or LDPE.
  • The ethylene monomer has two hydrogen atoms bonded to each carbon for a total of four hydrogen atoms that are not involved in the formation of the polymer. Many other polymers can be formed when one or more of these hydrogen atoms are replaced by some other atom or group of atoms.
  • Natural and synthetic rubbers are both addition polymers. Natural rubber is obtained from the sap that oozes from rubber trees. It was named by Joseph Priestley who used it to rub out pencil marks, hence, its name, a rubber. Natural rubber can be decomposed to yield monomers of isoprene.
  • It was sticky and smelly when it got too hot and it got hard and brittle in cold weather. These undesirable properties were eliminated when, in 1839, Charles Goodyear accidentally spilled a mixture of rubber and sulfur onto a hot stove and found that it did not melt but rather formed a much stronger but still elastic product. The process, called vulcanization, led to a more stable rubber product that withstood heat (without getting sticky) and cold (without getting hard) as well as being able to recover its original shape after being stretched. The sulfur makes cross-links in the long polymer chain and helps give it strength and resiliency, that is, if stretched, it will spring back to its original shape when the stress is released.
  • A second method by which monomers bond together to form polymers is called condensation.
  • Unlike addition polymers, in which all the atoms of the monomers are present in the polymer, two products result from the formation of condensation polymers, the polymer itself and another small molecule which is often, but not always, water.
  • One of the simplest of the condensation polymers is a type of nylon called nylon 6.
  • All amino acids molecules have an amine group (NH2) at one end and a carboxylic acid (COOH) group at the other end. A polymer forms when a hydrogen atom from the amine end of one molecule and an oxygen-hydrogen group (OH) from the carboxylic acid end of a second molecule split off and form a water molecule. The monomers join together as a new chemical bond forms between the nitrogen and carbon atoms. This new bond is called an amide linkage.
  • The new molecule, just like each of the monomers from which it formed, also has an amine group at one end (that can add to the carboxylic acid group of another monomer) and it has a carboxylic acid group at the other end (that can add to the amine end of another monomer). The chain can continue to grow and form very large polymers.
  • Polymers formed by this kind of condensation reaction are referred to as polyamides.
  • Nylon became a commercial product for Du Pont when their research scientists were able to draw it into long, thin, symmetrical filaments. As these polymer chains line up side-by-side, weak chemical bonds called hydrogen bonds form between adjacent chains. This makes the filaments very strong.
  • Another similar polymer of the polyamide type is the extremely light-weight but strong material known as Kevlar. It is used in bullet-proof vests, aircraft, and in recreational uses such as canoes. Like nylon, one of the monomers from which it is made is terephthalic acid. The other one is phenylenediamine.
  • Polyesters are another type of condensation polymer, so-called because the linkages formed when the monomers join together are called esters.
  • Probably the best known polyester is known by its trade name, Dacron.
  • Dacron is used primarily in fabrics and clear beverage bottles. Films of Dacron can be coated with metallic oxides, rolled into very thin sheets (only about one-thirtieth the thickness of a human hair), magnetized, and used to make audio and video tapes. When used in this way, it is extremely strong and goes by the trade name Mylar. Because it is not chemically reactive, and is not toxic, allergenic, or flammable, and because it does not promote blood-clotting, it can be used to replace human blood vessels when they are severely blocked and damaged or to replace the skin of burn victims.
Becky Kriger

Polymer Tutorial - 0 views

  • "Poly" means "many" and "mer" means "parts.
  • The parts are usually the same part used repeatedly in a chain-like manner. Polymers are also referred to as plastics
  • Nature has many examples of polymers. Cotton fibers are made of sugar molecules that are repeated in a chain-like manner. Hair, wool, and other natural fibers are polymers.
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  • Now be aware that one of the connecting sticks can spring open. To see animation of this, move cursor over the image. As long as cursor is over image, animation repeats
  • 1) We start with several pairs of balls each with two connecting sticks. 2) Something causes one of the connecting sticks to fling open. It then connects to another ball, but in doing so, causes one of its connecting sticks to fling open. 3) In moments all of the pairs of balls are now connected. Move cursor over image to see animation.
  • Sometimes heat, high energy light, or something else causes the double-bond to break and two of the middle 4 electrons split up and end up on the two outer ends of the molecule. These electrons are unpaired, which makes them eager to join with another electron.
  • (place cursor over the image to see animated version)
  • The unpaired electron triggers the ethylene molecule that bumps into it, to shift the inside electron to pair with it. That then causes the newly unpaired inner electron to move to the outside and it is now an unpaired electron ready to cause the next ethylene molecule to repeat the process.
  • The name of this polymer is appropriately called, polyethylene.
  • This is called high density polyethylene (HDPE).
  • High density polyethylene HDPE is used for bottles, buckets, jugs, containers, toys, even synthetic lumber, and many other things.
  • Sometimes the chains get up to 500,000 carbons long. Here they are tough enough for synthetic ice, replacement joints and bullet-proof vests. This is called Ultra High Molecular Weight PolyEthylene or UHMWPE.
  • low density polyethylene (LDPE).
  • It is made by causing the long chains of ethylene to branch. That way they cannot lie next each other, which reduces the density of the polyethylene. This makes the plastic lighter and more flexible.
  • Low density polyethylene is used to make plastic bags, plastic wrap, and squeeze bottles, plus many other things.
  • The favorite properties of plastics are that they are inert and won't react with what is stored in them. They also are durable and won't easily decay, dissolve, or break apart. These are great qualities for things you keep, but when you throw them away, they won't decompose.
  • The answer is to recycle the plastics. Here we see a bunch of CDs getting recycled.
  • Here are two recycle code drawings. You already know about HDPE and LDPE.
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    A simply explained introduction to polymers.
Becky Kriger

OChem- Biopolymers - 0 views

  • The red lines connecting the 4th carbon atom of one isoprene unit with the 1st carbon of the next indicate that latex is an addition polymer that results from the 1,4-addition of one isoprene unit to the next. Note the head-to-tail pattern in which the isoprene units are connected. Note, too, that the stereochemistry is the same at each double bond, namely cis.
  • Synthetic Rubber In 1839 Charles Goodyear discovered, literally by accident, that heating natural rubber with elemental sulfur altered the properties of the polymer, most notably making it tougher and more elastic. Goodyear's discovery led to the development of synthetic rubber, a material that found its most profitable application in the manufacture of automobile tires. Investigation of the structure of synthetic rubber revealed that the sulfur had formed disulfide bonds that linked one polyisoprene chain to the next. As Figure 2 demonstrates, these cross-links serve to restore the polymer to its original shape after it has been deformed by the application of a force. Figure 2 Bouncing Back
  • Not surprisingly, the desireable properties of natural as well as synthetic rubber led to investigations of the polymerization of structural analogs of isoprene. One notable success came from the polymerization of 2-chloro-1,3-butadiene, sometimes called chloroprene. Polychloroprene is known commercially as neoprene rubber. It is widely used in the automotive industry for the manufacture of oil-resistant hoses. Neoprene that contains entrapped air has good insulating properties and is used in the production of wet suits.
Becky Kriger

Thermosetting plastic - Plastics Wiki - 0 views

  • Thermosetting plastics (thermosets) refer to a variety of polymer materials that cure, through the addition of energy, to a stronger form.
  • Thermoset materials are usually liquid, powder, or malleable prior to curing, and designed to be molded into their final form, or used as adhesives.
  • The curing process transforms the resin into a plastic or rubber by cross-linking. Energy and catalysts are added that cause the molecular chains to link into a rigid, 3-D structure.
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  • Thermoset materials are generally stronger than thermoplastic materials, and are also better suited to high-temperature applications. They do not lend themselves to recycling like thermoplastics, which can be melted and re-molded.
  • Examples Natural Rubber Bakelite, a Phenol Formaldehyde Resin (used in electrical insulators and plastic wear) Duroplast Urea-Formaldehyde Foam (used in plywood, particleboard and medium-density fibreboard) Melamine (used on worktop surfaces) Polyester Resin (used in glass-reinforced plastics/Fibreglass (GRP)) Epoxy Resin (used as an adhesive and in fibre reinforced plastics such as glass reinforced plastic and graphite-reinforced plastic)
Becky Kriger

Scientific Principles:Polymers - 0 views

  • The chemical reaction in which high molecular mass molecules are formed from monomers is known as polymerization. There are two basic types of polymerization, chain-reaction (or addition) and step-reaction (or condensation) polymerization.
  • One of the most common types of polymer reactions is chain-reaction (addition) polymerization. This type of polymerization is a three step process involving two chemical entities. The first, known simply as a monomer, can be regarded as one link in a polymer chain. It initially exists as simple units. In nearly all cases, the monomers have at least one carbon-carbon double bond. Ethylene is one example of a monomer used to make a common polymer.
  • The other chemical reactant is a catalyst. In chain-reaction polymerization, the catalyst can be a free-radical peroxide added in relatively low concentrations. A free-radical is a chemical component that contains a free electron that forms a covalent bond with an electron on another molecule. The formation of a free radical from an organic peroxide is shown below:
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  • The first step in the chain-reaction polymerization process, initiation, occurs when the free-radical catalyst reacts with a double bonded carbon monomer, beginning the polymer chain. The double carbon bond breaks apart, the monomer bonds to the free radical, and the free electron is transferred to the outside carbon atom in this reaction.
  • The next step in the process, propagation, is a repetitive operation in which the physical chain of the polymer is formed. The double bond of successive monomers is opened up when the monomer is reacted to the reactive polymer chain. The free electron is successively passed down the line of the chain to the outside carbon atom.
  • Thermodynamically speaking, the sum of the energies of the polymer is less than the sum of the energies of the individual monomers. Simply put, the single bounds in the polymeric chain are more stable than the double bonds of the monomer.
  • Termination occurs when another free radical (R-O.), left over from the original splitting of the organic peroxide, meets the end of the growing chain. This free-radical terminates the chain by linking with the last CH2. component of the polymer chain. This reaction produces a complete polymer chain. Termination can also occur when two unfinished chains bond together. Both termination types are diagrammed below. Other types of termination are also possible.
  • This exothermic reaction occurs extremely fast, forming individual chains of polyethylene often in less than 0.1 second.
  • Step-reaction (condensation) polymerization is another common type of polymerization. This polymerization method typically produces polymers of lower molecular weight than chain reactions and requires higher temperatures to occur. Unlike addition polymerization, step-wise reactions involve two different types of di-functional monomers or end groups that react with one another, forming a chain. Condensation polymerization also produces a small molecular by-product (water, HCl, etc.).
  • As indicated above, both addition and condensation polymers can be linear, branched, or cross-linked. Linear polymers are made up of one long continuous chain, without any excess appendages or attachments. Branched polymers have a chain structure that consists of one main chain of molecules with smaller molecular chains branching from it. A branched chain-structure tends to lower the degree of crystallinity and density of a polymer. Cross-linking in polymers occurs when primary valence bonds are formed between separate polymer chain molecules. Chains with only one type of monomer are known as homopolymers. If two or more different type monomers are involved, the resulting copolymer can have several configurations or arrangements of the monomers along the chain. The four main configurations are depicted below:
  • They can be found in either crystalline or amorphous forms. Crystalline polymers are only possible if there is a regular chemical structure (e.g., homopolymers or alternating copolymers), and the chains possess a highly ordered arrangement of their segments. Crystallinity in polymers is favored in symmetrical polymer chains, however, it is never 100%. These semi-crystalline polymers possess a rather typical liquefaction pathway, retaining their solid state until they reach their melting point at Tm.
  • Amorphous polymers do not show order. The molecular segments in amorphous polymers or the amorphous domains of semi-crystalline polymers are randomly arranged and entangled. Amorphous polymers do not have a definable Tm due to their randomness
  • At low temperatures, below their glass transition temperature (Tg), the segments are immobile and the sample is often brittle. As temperatures increase close to Tg, the molecular segments can begin to move. Above Tg, the mobility is sufficient (if no crystals are present) that the polymer can flow as a highly viscous liquid.
  • Thermoplastics are generally carbon containing polymers synthesized by addition or condensation polymerization. This process forms strong covalent bonds within the chains and weaker secondary Van der Waals bonds between the chains. Usually, these secondary forces can be easily overcome by thermal energy, making thermoplastics moldable at high temperatures.
  • Thermosets have the same Van der Waals bonds that thermoplastics do. They also have a stronger linkage to other chains. Strong covalent bonds chemically hold different chains together in a thermoset material. The chains may be directly bonded to each other or be bonded through other molecules. This "cross-linking" between the chains allows the material to resist softening upon heating.
  • Compression Molding This type of molding was among the first to be used to form plastics. It involves four steps: Pre-formed blanks, powders or pellets are placed in the bottom section of a heated mold or die. The other half of the mold is lowered and is pressure applied. The material softens under heat and pressure, flowing to fill the mold. Excess is squeezed from the mold. If a thermoset, cross-linking occurs in the mold. The mold is opened and the part is removed. For thermoplastics, the mold is cooled before removal so the part will not lose its shape. Thermosets may be ejected while they are hot and after curing is complete. This process is slow
  • Injection Molding This very common process for forming plastics involves four steps: Powder or pelletized polymer is heated to the liquid state. Under pressure, the liquid polymer is forced into a mold through an opening, called a sprue. Gates control the flow of material. The pressurized material is held in the mold until it solidifies. The mold is opened and the part removed by ejector pins. Advantages of injection molding include rapid processing, little waste, and easy automation.
  • Transfer Molding This process is a modification of compression molding. It is used primarily to produce thermosetting plastics. Its steps are: A partially polymerized material is placed in a heated chamber. A plunger forces the flowing material into molds. The material flows through sprues, runners and gates. The temperature and pressure inside the mold are higher than in the heated chamber, which induces cross-linking. The plastic cures, is hardened, the mold opened, and the part removed. Mold costs are expensive and much scrap material collects in the sprues and runners, but complex parts of varying thickness can be accurately produced.
  • Extrusion This process makes parts of constant cross section like pipes and rods. Molten polymer goes through a die to produce a final shape. It involves four steps: Pellets of the polymer are mixed with coloring and additives. The material is heated to its proper plasticity. The material is forced through a die. The material is cooled.
  • Blow Molding Blow molding produces bottles, globe light fixtures, tubs, automobile gasoline tanks, and drums. It involves: A softened plastic tube is extruded The tube is clamped at one end and inflated to fill a mold. Solid shell plastics are removed from the mold. This process is rapid and relatively inexpensive.
  • In 1989, a billion pounds of virgin PET were used to make beverage bottles of which about 20% was recycled. Of the amount recycled, 50% was used for fiberfill and strapping. The reprocessors claim to make a high quality, 99% pure, granulated PET. It sells at 35 to 60% of virgin PET costs. The major reuses of PET include sheet, fiber, film, and extrusions.
  • Of the plastics that have a potential for recycling, the rigid HDPE container is the one most likely to be found in a landfill. Less than 5% of HDPE containers are treated or processed in a manner that makes recycling easy.
  • There is a great potential for the use of recycled HDPE in base cups, drainage pipes, flower pots, plastic lumber, trash cans, automotive mud flaps, kitchen drain boards, beverage bottle crates, and pallets.
  • LDPE is recycled by giant resin suppliers and merchant processors either by burning it as a fuel for energy or reusing it in trash bags. Recycling trash bags is a big business.
  • There is much controversy concerning the recycling and reuse of PVC due to health and safety issues. When PVC is burned, the effects on the incinerator and quality of the air are often questioned. The Federal Food and Drug Administration (FDA) has ordered its staff to prepare environmental impact statements covering PVC's role in landfills and incineration. The burning of PVC releases toxic dioxins, furans, and hydrogen chloride.
  • PVC is used in food and alcoholic beverage containers with FDA approval. The future of PVC rests in the hands of the plastics industry to resolve the issue of the toxic effects of the incineration of PVC. It is of interest to note that PVC accounts for less than 1% of land fill waste.
  • PS and its manufacturers have been the target of environmentalists for several years. The manufacturers and recyclers are working hard to make recycling of PS as common as that of paper and metals. One company, Rubbermaid, is testing reclaimed PS in service trays and other utility items.
  • Table 3: Major Plastic Resins and Their Uses Resin CodeResin NameCommon UsesExamples of Recycled Products Polyethylene Terephthalate (PET or PETE) Soft drink bottles, peanut butter jars, salad dressing bottles, mouth wash jars Liquid soap bottles, strapping, fiberfill for winter coats, surfboards, paint brushes, fuzz on tennis balls, soft drink bottles, film High density Polyethylene (HDPE) Milk, water, and juice containers, grocery bags, toys, liquid detergent bottles Soft drink based cups, flower pots, drain pipes, signs, stadium seats, trash cans, re-cycling bins, traffic barrier cones, golf bag liners, toys Polyvinyl Chloride or Vinyl (PVC-V) Clear food packaging, shampoo bottles Floor mats, pipes, hoses, mud flaps Low density Polyethylene (LDPE) Bread bags, frozen food bags, grocery bags Garbage can liners, grocery bags, multi purpose bags Polypropylene (PP) Ketchup bottles, yogurt containers, margarine, tubs, medicine bottles Manhole steps, paint buckets, videocassette storage cases, ice scrapers, fast food trays, lawn mower wheels, automobile battery parts. Polystyrene (PS) Video cassette cases, compact disk jackets, coffee cups, cutlery, cafeteria trays, grocery store meat trays, fast-food sandwich container License plate holders, golf course and septic tank drainage systems, desk top accessories, hanging files, food service trays, flower pots, trash cans
Becky Kriger

Chemistry - Condensation polymer - 0 views

  • Condensation polymers are any class of polymer formed through a condensation reaction, as opposed to addition polymers which involve the reaction of unsaturated monomers. Types of condensation polymer include polyamides and polyesters.
  • The carboxylic acids and amines link to form peptide bonds, also known as amide groups. Proteins are condensation polymers made from amino acid monomers. Carbohydrates are also condensation polymers made from sugar monomers such as glucose and galactose.
  • Condensation Polymers, unlike Addition polymers are bio-degradable. The peptide or ester bonds between monomers can be hydrolysed by acid catalysts or bacterial enzymes breaking the polymer chain into smaller pieces.
Becky Kriger

Plastics - 0 views

  • lastics are synthetic materials, which means that they are artificial, or manufactured.
  • he building blocks for making plastics are small organic molecules - molecules that contain carbon along with other substances. They generally come from oil (petroleum) or natural gas, but they can also come from other organic materials such as wood fibers, corn, or banana peels! Each of these small molecules is known as a monomer ("one part") because it's capable of joining with other monomers to form very long molecule chains called polymers ("many parts")
  • 1. Crude oil, the unprocessed oil that comes out of the ground, contains hundreds of different hydrocarbons, as well as small amounts of other materials. The job of an oil refinery is to separate these materials and also to break down (or "crack) large hydrocarbons into smaller ones. 2. A petrochemical plant receives refined oil containing the small monomers they need and creates polymers through chemical reactions. 3. A plastics factory buys the end products of a petrochemical plant - polymers in the form of resins - introduces additives to modify or obtain desirable properties, then molds or otherwise forms the final plastic products.
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  • One such molecule is the ethylene monomer, the starting point for a variety of plastics. Ethylene is a small hydrocarbon consisting of four hydrogen atoms and two carbon atoms.
  • Polymerization is often started by combining the monomers through the use of a catalyst - a substance that aids a chemical reaction without undergoing any permanent chemical change itself. During the chemical reaction, hundreds or thousands of monomers combine to form a polymer chain, and millions of polymer chains are formed at the same time. The mass of polymers that results is known as a resin.
  • Polyethylene is made from just ethylene monomers - but it's also possible to create polymers from two or more different monomers. You can make hundreds of different polymers depending on which monomers and catalysts you use.
  • Cellulose, the basic component of plant cell walls is a polymer, and so are all the proteins produced in your body and the proteins you eat. Another famous example of a polymer is DNA - the long molecule in the nuclei of your cells that carries all the genetic information about you.
  • lastics are classified into two categories according to what happens to them when they're heated to high temperatures. Thermoplastics keep their plastic properties: They melt when heated, then harden again when cooled. Thermosets, on the other hand, are permanently "set" once they're initially formed and can't be melted. If they're exposed to enough heat, they'll crack or become charred.
  • Thermoplastics have long, linear polymer chains that are only weakly chemically bonded, or connected, to each other. When a thermoplastic object is heated, these bonds are easily broken, which makes the polymers able to glide past each other like strands of freshly cooked spaghetti. That's why thermoplastics can readily be remolded. The weak bonds between the polymers reform when the plastic object is cooled, which enable it to keep its new shape.
  • The linear chains are crosslinked - strongly chemically bonded. This prevents a thermoplastic object from being melted and reformed.
  • The most common method for making plastics is molding. To make a thermoplastic object, plastic granules known as resin are forced into a mold under high heat and pressure. When the material has cooled down, the mold is opened and the plastic object is complete. When making plastic fibers, the molten resin is sprayed through a strainer with tiny holes.
  • Thermosets are produced in two steps: 1. Linear polymers are formed. 2. The linear polymers are forced into a mold where "curing" takes place. This may involve heating, pressure, and the addition of catalysts. During this process, a cross-linked or networked structure forms, creating a permanently hard object that is no longer meltable or moldable.
  • For most applications, the ideal polymer is a long, straight chain with a highly regular molecular structure. Early synthetic polymers, however, often exhibited odd little branches and other irregularities. In the 1950s, German chemist Karl Ziegler (1898–1973) discovered that an entirely different type of catalyst - a combination of aluminum compounds with other metallic compounds - could solve some of these annoying problems and increase the length of a polymer chain, producing superior plastics.
  • olymers often have short side chains, which can occur on either side of the main chain. If side branches occur randomly to the left or right, the polymer has an irregular structure. Italian chemist Giulio Natta (1903–1979) discovered that some Ziegler catalysts led to a uniform structure in which all the side branches are on the same side.
  • Firstly, there is an environmental impact from plastics production; however the plastics industry has worked hard to reduce energy and water use, as well as waste generation during the manufacturing processes.
  • Secondly, during their lives, plastic products can save energy and reduce carbon dioxide emissions in a variety of ways. For example, they're lightweight, so transporting them is energy efficient. And plastic parts in cars and airplanes reduce the weight of those vehicles and therefore less energy is needed to operate them and lower emissions are created.
Becky Kriger

Biopolymers and Bioplastics - 0 views

  • Biopolymers are polymers which are present in, or created by, living organisms. These include polymers from renewable resources that can be polymerized to create bioplastics. Bioplastics are plastics manufactured using biopolymers, and are biodegradable.
  • There are two main types of biopolymers: those that come from living organisms; and, those which need to be polymerized but come from renewable resources. Both types are used in the production of bioplastics
  • Biopolymer Natural Source What is it? Cellulose Wood, cotton, corn, wheat, and others This polymer is made up of glucose. It is the main component of plant cell walls. Soy protein Soybeans Protein which naturally occurs in the soy plant. Starch Corn, potatoes, wheat, tapioca, and others This polymer is one way carbohydrates are stored in plant tissue. It is a polymer made up of glucose. It is not found in animal tissues. Polyesters Bacteria These polyesters are created through naturally occurring chemical reactions that are carried out by certain types of bacteria.
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  • Biopolymer Natural Source What is it? Lactic Acid Beets, corn, potatoes, and others Produced through fermentation of sugar feedstocks, such as beets, and by converting starch in corn, potatoes, or other starch sources. It is polymerized to produce polylactic acid -- a polymer that is used to produce plastic. Triglycerides Vegetable oils These form a large part of the storage lipids found in plant and animal cells. Vegetable oils are one possible source of triglycerides that can be polymerized into plastics.
  • Using Fermentation to Produce Plastics Fermentation, used for hundreds of years by humans, is even more powerful when coupled with new biotechnology techniques.
  • Today, fermentation can be carried out with genetically engineered microorganisms, specially designed for the conditions under which fermentation takes place,
  • Fermentation, in fact, is the process by which bacteria can be used to create polyesters. Bacteria called Ralstonia eutropha are used to do this. The bacteria use the sugar of harvested plants, such as corn, to fuel their cellular processes. The by-product of these cellular processes is the polymer.
  • Lactic acid is fermented from sugar, much like the process used to directly manufacture polymers by bacteria. However, in this fermentation process, the final product of fermentation is lactic acid, rather than a polymer. After the lactic acid is produced, it is converted to polylactic acid using traditional polymerization processes.
  • Plants are becoming factories for the production of plastics. Researchers created a Arabidopis thaliana plant through genetic engineering. The plant contains the enzymes used by bacteria to create plastics. Bacteria create the plastic through the conversion of sunlight into energy. The researchers have transferred the gene that codes for this enzyme into the plant, as a result the plant produces plastic through its cellular processes. The plant is harvested and the plastic is extracted from it using a solvent. The liquid resulting from this process is distilled to separate the solvent from the plastic.
  • Currently, fossil fuel is still used as an energy source during the production process. This has raised questions by some regarding how much fossil fuel is actually saved by manufacturing bioplastics. Only a few processes have emerged that actually use less energy in the production process.
  • Energy use is not the only concern when it comes to biopolymers and bioplastics. There are also concerns about how to balance the need to grow plants for food, and the need to grow plants for use as raw materials. Agricultural space needs to be shared. Researchers are looking into creating a plant that can be used for food, but also as feedstock for plastic production.
  • Biopolymers and bioplastics are the main components in creating a sustainable plastics industry. These products reduce the dependence on non-renewable fossil fuels, and are easily biodegradable. Together, this greatly limits the environmental impacts of plastic use and manufacture. Also, characteristics such as being biodegradable make plastics more acceptable for long term use by society. It is likely that in the long term, these products will mean plastics will remain affordable, even as fossil fuel reserves diminish.
Becky Kriger

Recycling Plastics - How to Recycle Different Types of Plastic - 0 views

  • The easiest and most common plastics to recycle are made of polyethylene terephthalate (PETE) and are assigned the number 1. Examples include soda and water bottles, medicine containers, and many other common consumer product containers. Once it has been processed by a recycling facility, PETE can become fiberfill for winter coats, sleeping bags and life jackets. It can also be used to make bean bags, rope, car bumpers, tennis ball felt, combs, cassette tapes, sails for boats, furniture and, of course, other plastic bottles.
  • Number 2 is reserved for high-density polyethylene plastics. These include heavier containers that hold laundry detergents and bleaches as well as milk, shampoo and motor oil. Plastic labeled with the number 2 is often recycled into toys, piping, plastic lumber and rope.
  • Polyvinyl chloride, commonly used in plastic pipes, shower curtains, medical tubing, vinyl dashboards, and even some baby bottle nipples, gets number 3. Like numbers 4 (wrapping films, grocery and sandwich bags, and other containers made of low-density polyethylene) and 5 (polypropylene containers used in Tupperware, among other products), few municipal recycling centers will accept it due to its very low rate of recyclability.
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  • Number 6 goes on polystyrene (Styrofoam) items such as coffee cups, disposable cutlery, meat trays, packing “peanuts” and insulation. It is widely accepted because it can be reprocessed into many items, including cassette tapes and rigid foam insulation.
  • Usually imprinted with a number 7 or nothing at all, these plastics are the most difficult to recycle and, as such, are seldom collected or recycled.
Becky Kriger

Biodegradable plastics made from corn - 0 views

  • Biodegradable plastics have already been created by using proteins from plants such as corn or soy. But they were not strong enough to be used by the industry. Now, researchers at Iowa State University have found a way to reinforce these biorenewable plastics. They are using high-powered ultrasonics to reinforce the plastics with nanoclays.
  • But how biodegradable plastics can be made with corn proteins? Grewell keeps a plastic model of a molecule looking like a ball. That's about the shape of a soy or corn protein […] Then he unfolded the model into a long, straight loop. That's what happens when researchers add some glycerin — a byproduct of biodiesel production – and some water to the molecule.
  • Nanoclays are clays from the smectite family which have a unique morphology: they form platelets about 1 nanometer thick and 100 nanometers in diameter. Below is an example of the structure of one nanoclay raw material named montmorillonite.
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  • Apparently, it's difficult to use these nanoclays. So the researchers turned to "high-powered ultrasonics — high-frequency sound waves too high for human hearing – to separate and disperse the platelets."
Becky Kriger

Polysaccharides - Chemistry Encyclopedia - 0 views

  • Polysaccharides are long polymers of monosaccharides and their derivatives. Unlike proteins or nucleic acids, these polymers can be either linear or branched, and they can contain only one type of monosaccharide (homopolysaccharides), or more than one (heteropolysaccharides)
  • Starch is a homopolysaccharide and has two forms: amylopectin and α-amylose. In nature, starch is approximately 10 to 30 percent α-amylose.
  • Starch is the main energy reserve in plants; glycogen is the main energy reserve in animals
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  • In contrast to amylopectin, which comprises 70 to 90 percent of natural starch, α-amylose is a branching polysaccharide.
  • Branches occur at every twelve to thirty residues along a chain of α (1→4) linked glucoses. As a result, amylopectin has one reducing end and many nonreducing ends.
  • Amylopectin and α-amylose are broken down by the enzyme amylase. In animals, salivary α-amylase begins the digestion process in the mouth. Pancreatic α-amylase continues the process in the intestine.
  • Glycogen is the energy storage carbohydrate in animals. Glycogen is found mainly in the liver (where it is responsible for up to 10 percent of liver mass) and skeletal muscle (1 to 2 percent of skeletal muscle mass)
  • However, glycogen branches more abundantly than amylopectin, with branches at every eight to twelve residues. As a result, it has many more nonreducing ends. Glycogen is broken down at these nonreducing ends by the enzyme glycogen phosphorylase to release glucose for energy.
  • The primary structural homopolysaccharides are cellulose and chitin. Cellulose, a major component of plant cell walls, is the most abundant natural polymer on Earth.
  • Like α-amylose, cellulose is a linear polysaccharide composed entirely of glucose. However, in cellulose the glucose residues occur in β(1→4) linkage rather than α (1→4) (see Figure 1).
  • In addition, individual cellulose strands can form hydrogen bonds with one another to provide additional strength. Most animals, including humans, lack the enzymes necessary to dissolve α(1→4) linkages and so cannot digest cellulose
  • The animals that can (such as ruminants) do so via a symbiosis with bacteria that secrete cellulose-degrading enzymes.
  • The second most abundant polymer on Earth is chitin. Chitin comprises much of the exoskeletons of crustaceans, insects, and spiders, as well as the cell walls of fungi. Structurally, chitin is very similar to cellulose, except that its basic monosaccharide is N-acetylglucosamine
Becky Kriger

Polypeptides - 0 views

  • Polypeptides are chains of amino acids. Proteins are made up of one or more polypeptide molecules.
  • One end of every polypeptide, called the amino terminal or N-terminal, has a free amino group. The other end, with its free carboxyl group, is called the carboxyl terminal or C-terminal.
  • he sequence of amino acids in a polypeptide is dictated by the codons in the messenger RNA (mRNA) molecules from which the polypeptide was translated. The sequence of codons in the mRNA was, in turn, dictated by the sequence of codons in the DNA from which the mRNA was transcribed. The schematic below shows the N-terminal at the upper left and the C-terminal at the lower right.
Becky Kriger

Special Properties of Polymers - 0 views

shared by Becky Kriger on 08 Dec 08 - Cached
  • why these polymers, these macromolecules, act differently from small molecules.
  • Chain entanglement Summation of intermolecular forces Time scale of motion
  • Remember now that most polymers are linear polymers; that is, they are molecules whose atoms are joined in a long line to form a huge chain. Now most of the time, but not always, this chain is not stiff and straight, but is flexible. It twists and bends around to form a tangled mess.
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  • when a polymer is molten, the chains will act like spaghetti tangled up on a plate. If you try to pull out any one strand of spaghetti, it slides right out with no problem. But when polymers are cold and in the solid state, they act more like a ball of string.
  • intermolecular forces affect polymers just like small molecules. But with polymers, these forces are greatly compounded. The bigger the molecule, the more molecule there is to exert an intermolecular force. Even when only weak Van der Waals forces are at play, they can be very strong in binding different polymer chains together. This is another reason why polymers can be very strong as materials. Polyethylene, for example is very nonpolar. It only has Van der Waals forces to play with, but it is so strong it's used to make bullet proof vests.
  • This is a fancy way of saying polymers move more slowly than small molecules do. Imagine you are a first grade teacher, and it's time to go to lunch. Your task is to get your kids from the classroom to the cafeteria, without losing any of them, and to do so with minimal damage to the territory you'll have to cover to get to the cafeteria. Keeping them in line is going to be difficult. Little kids love to run around every which way, jumping and hollering and bouncing this way and that. One way to put a stop to all this chaotic motion is to make all the kids join hands when you're walking them to lunch. This won't be easy rest assured, as there's always going to be a lot of little boys who are too macho to hold the hands of the girls next to them in line, and some who are too insecure in their manhood to hold anyone's hand. But once you get them to do this, their ability to run around is severely limited. Of course, their motion will still be chaotic. The chain of kids will curve and snake this way and that on its way to eat soybean patties disguised as who knows what. But the motion will be a lot slower. You see, if one kid gets a notion to just bolt off in one direction, he or she can't do it because he or she will be bogged down by the weight of all the other kids to which he or she is bound. Sure, the kid can deviate from the straight path, and make a few other kids do so, but the deviation will be far less than you'd bet if the kids weren't all linked together. It's the same way with molecules.
  • So then how does this make a polymeric material different from a material made of small molecules? This slow speed of motion makes polymers do some very unusual things. For one, if you dissolve a polymer in a solvent, the solution will be a lot more viscous than the pure solvent.
Becky Kriger

Polymer Structures - 0 views

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  • Although the fundamental property of bulk polymers is the degree of polymerization, the physical structure of the chain is also an important factor that determines the macroscopic properties.
  • Configuration refers to the order that is determined by chemical bonds. The configuration of a polymer cannot be altered unless chemical bonds are broken and reformed. Conformation refers to order that arises from the rotation of molecules about the single bonds. These two structures are studied below.
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  • The two types of polymer configurations are cis and trans. These structures can not be changed by physical means (e.g. rotation). The cis configuration arises when substituent groups are on the same side of a carbon-carbon double bond. Trans refers to the substituents on opposite sides of the double bond.
  • Three distinct structures can be obtained. Isotactic is an arrangement where all substituents are on the same side of the polymer chain. A syndiotactic polymer chain is composed of alternating groups and atactic is a random combination of the groups. The following diagram shows two of the three stereoisomers of polymer chain.
  • The ability of an atom to rotate this way relative to the atoms which it joins is known as an adjustment of the torsional angle. If the two atoms have other atoms or groups attached to them then configurations which vary in torsional angle are known as conformations.
  • different conformation may represent different potential energies of the molecule. There several possible generalized conformations: Anti (Trans), Eclipsed (Cis), and Gauche (+ or -). The following animation illustrates the differences between them.
  • The geometric arrangement of the bonds is not the only way the structure of a polymer can vary. A branched polymer is formed when there are "side chains" attached to a main chain. A simple example of a branched polymer is shown in the following diagram.
  • One of these types is called "star-branching". Star branching results when a polymerization starts with a single monomer and has branches radially outward from this point. Polymers with a high degree of branching are called dendrimers Often in these molecules, branches themselves have branches.
  • A separate kind of chain structure arises when more that one type of monomer is involved in the synthesis reaction. These polymers that incorporate more than one kind of monomer into their chain are called copolymers. There are three important types of copolymers. A random copolymer contains a random arrangement of the multiple monomers. A block copolymer contains blocks of monomers of the same type. Finally, a graft copolymer contains a main chain polymer consisting of one type of monomer with branches made up of other monomers. The following diagram displays the different types of copolymers.
  • In addition to the bonds which hold monomers together in a polymer chain, many polymers form bonds between neighboring chains. These bonds can be formed directly between the neighboring chains, or two chains may bond to a third common molecule.
  • Polymers with a high enough degree of cross-linking have "memory." When the polymer is stretched, the cross-links prevent the individual chains from sliding past each other. The chains may straighten out, but once the stress is removed they return to their original position and the object returns to its original shape.
  • In vulcanization, a series of cross-links are introduced into an elastomer to give it strength. This technique is commonly used to strengthen rubber.
  • Elastomers,or rubbery materials, have a loose cross-linked structure. This type of chain structure causes elastomers to possess memory. Typically, about 1 in 100 molecules are cross-linked
  • Natural and synthetic rubbers are both common examples of elastomers. Plastics are polymers which, under appropriate conditions of temperature and pressure, can be molded or shaped (such as blowing to form a film). In contrast to elastomers, plastics have a greater stiffness and lack reversible elasticity.
Becky Kriger

How Plastics Are Made - 0 views

  • The term "plastics" encompasses organic materials, such as the elements carbon (C), hydrogen (H), nitrogen (N), chlorine (Cl) and sulfur (S), which have properties similar to those naturally grown in organic materials such as wood, horn and rosin.
  • The plastic production process begins by heating the hydrocarbons in a "cracking process." Here, in the presence of a catalyst, larger molecules are broken down into smaller ones such as ethylene (ethene) C2H4, propylene (propene) C3H6, and butene C4H8 and other hydrocarbons.
  • Other examples of thermoset plastics and their product applications are: Polyurethanes: mattresses, cushions, insulation, ski boots, toys Unsaturated Polyesters: lacquers, varnishes, boat hulls, furniture,  Epoxies: glues, coating electrical circuits, helicopter blades
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  • Other examples of thermoplastics are: Polyethylene: packaging, electrical insulation, milk and water bottles, packaging film, house wrap, agricultural film Polypropylene: carpet fibers, automotive bumpers, microwave containers, external prostheses Polyvinyl chloride (PVC): sheathing for electrical cables, floor and wall coverings, siding, credit cards, automobile instrument panels
  • These monomers are then chemically bonded into chains called polymers.
  • The resulting resins may be molded or formed to produce several different kinds of plastic products with application in many major markets. The variability of resin permits a compound to be tailored to a specific design or performance requirement.
  • Polymers are created by the chemical bonding of many identical or related basic units and those produced from a single monomer type are called homopolymers. These polymers are specifically made of small units bonded into long chains. Carbon makes up the backbone of the molecule and hydrogen atoms are bonded along the carbon backbone.
  • In order to achieve a commercial product, the plastic is subject to further treatment and the inclusion of additives which are selected to give it specified properties
  • Additives are incorporated into polymers to alter and improve their basic mechanical, physical or chemical properties. Additives are also used to protect the polymer from the degrading effects of light, heat, or bacteria; to change such polymer properties as flow; to provide product color; and to provide special characteristics such as improved surface appearance or reduced friction.
  • Types of Additives:     antioxidants: for outside application,      colorants: for colored plastic parts, foaming agents: for Styrofoam cups,      plasticizers: used in toys and food processing equipment
  • A Thermoset is a polymer that solidifies or "sets" irreversibly when heated. Similar to the relationship between a raw and a cooked egg, once heated, a thermoset polymer can't be softened again and once cooked, the egg cannot revert back to its original form.
  • A Thermoplastic is a polymer in which the molecules are held together by weak secondary bonding forces that soften when exposed to heat and return to its original condition when cooled back down to room temperature. When a thermoplastic is softened by heat, it can then be shaped by extrusion, molding or pressing. Ice cubes are a common household item which exemplify the thermoplastic principle. Ice will melt when heated but readily solidifies when cooled.
  • In this method, a separate molding and cooling station on the equipment allows the parison to be continuously formed.  This technique is used mainly for small thin-walled parts ranging up to containers with five gallon capacities.  Parison programming can be used to vary the wall thickness.  Continuous extrusion also allows the use of heat-sensitive materials due to streamlined flow areas and die designs.
  • This technique is performed in three basic ways --reciprocating, ram accumulator, and accumulator head systems.  All three vary in machine design and the flow of molten resin through the die for parison forming.  However, each system is designed to produce larger, heavier, and thicker parts than continuous extrusion.
  • Blow moldable grades of material are initially injection molded into preform shapes.  These preforms are then thermally conditioned and then stretched (utilizing pneumatically operated stretch rods) low pressure air, followed by high pressure air up to 40 bar to form axially oriented parts with molded in necks.  The process is used to manufacture PET bottles.
  • This process utilizes various thermoplastic materials in a solid pelletized state and converts these materials by way of heat, pressure and compressed air into a finished good stat.The pellitized raw material is conveyed to the feed section of a plasticating extruder by way of a vacuum loader or auger screw.  The raw material is then conveyed forward through the extruder and is plastisized to a molten state of between 350 degrees and 500 degrees F. by way of a feed screw and external heating elements.The material in a melt state is then reshaped into a round hollow geometry termed a parison.  This parison is then extruded vertically from the head section of the machine through a round die at various outside and inside diameters.After extrusion of the parison between the two halves of a mold the press section closes encapsulating the parison inside the mold halves.  Upon mold close compressed air is entered into the parison by way of a centrally located air pipe or by piercing air needles.The molds are chilled with cooled water which transfers the hear form the now formed part inside the mold.  Upon complete part cooling the press section opens and the finished product is removed.  The material which is pinched off outside the mold cavity, or the flash, is then fed into a granulator which cops the flash into a granule size which can be fed back to the feed section of the extruder.
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