Polymerizes To Form Polyethylene

Transcription

Polymerizes to form polyethylene

Ethylene polymerizes to form polyethylene. Is polyethylene fuel resistant. Why does butane not form polymers. Polymerizes to form polyethylene physical or chemical. How to make polyethylene biodegradable.Figure 18.6 shows a polyethylene polymer backbone with a large number of carbon atoms connected.From: Extrusion, 2005 Versatility, ease of manufacture, and relatively low cost make plastics some of the most useful materials for a wide range of applications. This article explains the chemistry and production processes behind two of the mostpopular plastics — polyethylene and polypropylene. Plastics are some of the world’s most diverse and useful manufacturing materials. While plastics encompass a large number of materials, polyethylene and polypropylene are two of the major plastic types found in many consumer goods, from car parts to shopping bags to water pipes. Several typesof reactors can make polymers, including fluidized-bed, loop, autoclave, and tubular reactors. Different grades of polyethylene and polypropylene offer a wide range of physical properties, such as density, stiffness, flexibility, opacity, melting point, texture, and strength. Manipulating variables in the reactor, such as monomer, comonomer, catalyst,and cooling media flowrates, can control key quality parameters. Additives and colorings can modify the appearance of the polymer. Polymer plants are semi-continuous processes. Raw material is fed into a reactor continuously at the front end, while polymer powder and pellets are packaged in batches. Most sites operate multiple lines with manybins and silos for storage and blending. The plastics are eventually delivered to customers using barges, trucks, or rail cars. This article describes the different polyolefin production processes, their key operating parameters, and ways to use automation for improved quality control and higher throughput. The chemistry of making plastic It’s helpful tounderstand some of the chemistry behind the polymerization reaction to appreciate how the process works and the complexity involved in making plastic. A polymerization reaction starts with a primary ingredient (monomer), such as ethylene or propylene. Ethylene (C2H4) is a stable molecule with two carbon atoms and a double bond. Polyethylene(PE) is a made by the reaction of multiple ethylene molecules in the presence of catalyst to break the double bond and connect the carbon atoms into a chain (Figure 1). The longer the chain, the higher the molecular weight. Polymers can have molecular weights in the millions. Similarly, polypropylene (PP) is made by breaking the double bond in apropylene (C3H6) molecule, in the presence of a catalyst, to form long chains of three-carbon-atom molecules (Figure 2). The third carbon atom adds a complexity: On which side of the chain will the methyl (CH3) groups fall? They could all be on one side of the chain’s centerline, or backbone (isotactic), they could appear alternately on opposite sidesof the backbone (syndiotactic), or their positions could be random (atactic). These arrangements have different physical properties. Polymerization reactions will also consume hydrogen, which is required to quench the reaction (i.e., end the chains), and some will involve a secondary ingredient (known as a comonomer). Since the concentrations ofthese components in the reactor affect the probabilities that specific reactions will take place, the composition in the reactor effectively sets the amount of branching and the length of the chain. Figure 1. Ethylene is a stable molecule with two carbon atoms connected by a double bond. Polyethylene is made by the reaction of multiple ethylenemolecules in the presence of catalyst. The polymer industry employs many catalysts, and new catalysts are developed every year. Different catalysts are used to create polymers with particular properties, even in the same reactor. Each PE or PP process licensor incorporates proprietary catalyst formulations in its reactor designs. Depending on thetype of reactor, the catalysts can be solid particles or suspended in hydrocarbon or solvent. Polymerization is a highly exothermic reaction, and it requires continuous cooling to prevent runaway reactions. Most reactor systems include an emergency quench that quickly shuts down the reactor if the temperature reaches a predetermined setpoint.Before the implementation of redundant control mechanisms, a runaway reaction could cause the reactor to become completely plugged with plastic. Process designs have since changed and safety systems have been implemented to prevent such incidents. Figure 2. Polypropylene is made by breaking the double bond in a propylene molecule in thepresence of a catalyst. The resulting polymer may be isotactic, with all of the methyl groups on the same side of the polymer backbone, syndiotactic, with alternate methyl groups on opposite sides of the backbone, or atactic (not shown), with the methyl groups arranged randomly. Figure 3. The molecular weight distribution of a bimodal polymer hasmore than one peak. Key quality specifications Although polymer properties can be modified somewhat in the blending and extruding steps, the conditions in the reactor set the product grade(s) — as defined by a few key quality measures — that can be made. In general, polyethylene is categorized based on its density, the linearity of the molecules(i.e., degree of branching), and its molecular weight (length of the chains). Other polymer qualities, including the molten flowing property, known as the melt-flow index, are a function of the crystalline structure and are also primarily determined by the polymerization reaction. The melt-flow index determines the polymer’s behavior in downstreamoperations, such as extrusion, blow molding, or film production. The most common polyethylene grades are: high-density polyethylene (HDPE). This polymer has a density greater than or equal to 0.941 g/cm3. It has a low degree of branching, with mostly linear molecules, has high tensile strength, is resistant to many chemicals, and is used in suchproducts as bottles, jugs, water pipes, and toys. medium-density polyethylene (MDPE). With a density range between 0.925 and 0.940 g/cm3, MDPE has better shock and stress crack resistance than HDPE and is commonly used for gas pipes, plastic bags, and packaging films. low-density polyethylene (LDPE). This grade has a density range of. Wereap the benefits of using Styrofoam containers, but don't often consider where they end up. Styrofoam materials do not break down quickly under exposure to the elements. When buried in a landfill, styrofoam will remain intact for a long time. The good news is that there is not a lot of this pollutant found in landfills (maybe about \(0.5\%\) by weightof the total mass of garbage). There is no good way to recycle Styrofoam at present, but in the future, a creative scientist may change that. Polymers are very different from the other kinds of organic molecules that you have seen so far. Whereas other compounds are of relatively low molar mass, polymers are giant molecules of very high molar mass.Polymers are the primary components of all sorts of plastics and related compounds. A polymer is a large molecule formed of many smaller molecules covalently bonded in a repeating pattern. The small molecules which make up the polymer are called monomers. Polymers generally form either from an addition reaction or a condensation reaction. Anaddition polymer is a polymer formed by chain addition reactions between monomers that contain a double bond. Molecules of ethene can polymerize with each other under the right conditions to form the polymer called polyethylene. \[n \ce{CH 2 CH 2} \rightarrow \ce{-(CH 2CH 2)} n-onumber \] The letter \(n\) stands for the number of monomersthat are joined in repeated fashion to make the polymer, and can have a value in the hundreds or even thousands. Figure \(\PageIndex{1}\): Polyethylene synthesis. The reactions above show the basic steps to form an addition polymer: Initiation - a free radical initiator \(\left( \ce{X} * \right)\) attacks the carbon-carbon double bond (first step above).The initiator can be something like hydrogen peroxide. This material can easily split to form two species with a free electron attached to each: \(\ce{H-O-O-H} \rightarrow 2 \ce{H-O} \cdot\). This free radical attacks a carbon-carbon double bond. One of the pi electrons forms a single bond with the initiator while the other pi electron forms a new freeradical on the carbon atom. Propagation - the new free radical compound interacts with another alkane, continuing the process of chain growth (second step above). Termination occurs whenever two free radicals come in contact with one another (not shown). The two free electrons form a covalent bond and the free radical on each molecule nolonger exists. Polyethylene can have different properties depending on the length of the polymer chains, and on how efficiently they pack together. Some common products made from different forms of polyethylene include plastic bottles, plastic bags, and harder plastic objects such as milk crates. Several other kinds of unsaturated monomers can bepolymerized, and are components in common household products. Polypropylene is stiffer than polyethylene, and is in plastic utensils and some other types of containers. Figure \(\PageIndex{2}\): Polypropylene structure. Polystyrene is used in insulation and in molded items such as coffee cups. Figure \(\PageIndex{3}\): Polystyrene synthesis and

structure. Polyvinyl chloride (PVC) is extensively used for plumbing pipes. Figure \(\PageIndex{4}\): Polyvinyl chloride. Polyisoprene is a polymer of isoprene and is better known as rubber. It is produced naturally by rubber trees, but several variants have been developed which demonstrate improvements on the properties of natural rubber. Figure \(\PageIndex{5}\): Polyisoprene. Summary A polymer is a large molecule formed of many smaller molecules covalently bonded in a repeating pattern; they are the primary components of all sorts of plastics and related compounds. The small molecules which make up polymers are called monomers. Polymers generally form either from an additionreaction or a condensation reaction. An addition polymer is a polymer formed by chain addition reactions between monomers that contain a double bond. The basic steps to form an addition polymer are: (1) initiation, (2) propagation, (3) termination LICENSED UNDER

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Ethylene polymerizes to form polyethylene. Is polyethylene fuel resistant. Why does butane not form polymers. Polymerizes to form polyethylene physical or chemical.