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Ziegler Catalyst Systems

Special catalyst system (Ziegler-Natta) required Three structures ... [Pg.111]

Before the development of the Ziegler-Natta catalyst systems (Section 6 21) polymer ization of propene was not a reaction of much value The reason for this has a stereo chemical basis Consider a section of polypropylene... [Pg.312]

Coordination polymerization of isoprene using Ziegler-Natta catalyst systems (Section 6 21) gives a material similar in properties to natural rubber as does polymerization of 1 3 butadiene Poly(1 3 buta diene) is produced in about two thirds the quantity of SBR each year It too finds its principal use in tires... [Pg.408]

Metal Alibis and Alkoxides. Metal alkyls (eg, aluminum boron, sine alkyls) are fairly active catalysts. Hyperconjugation with the electron-deficient metal atom, however, tends to decrease the electron deficiency. The effect is even stronger in alkoxides which are, therefore, fairly weak Lewis acids. The present discussion does not encompass catalyst systems of the Ziegler-Natta type (such as AIR. -H TiCl, although certain similarities with Friedel-Crafts systems are apparent. [Pg.564]

Catalysts. Iodine and its compounds ate very active catalysts for many reactions (133). The principal use is in the production of synthetic mbber via Ziegler-Natta catalysts systems. Also, iodine and certain iodides, eg, titanium tetraiodide [7720-83-4], are employed for producing stereospecific polymers, such as polybutadiene mbber (134) about 75% of the iodine consumed in catalysts is assumed to be used for polybutadiene and polyisoprene polymeri2a tion (66) (see RUBBER CHEMICALS). Hydrogen iodide is used as a catalyst in the manufacture of acetic acid from methanol (66). A 99% yield as acetic acid has been reported. In the heat stabiH2ation of nylon suitable for tire cordage, iodine is used in a system involving copper acetate or borate, and potassium iodide (66) (see Tire cords). [Pg.366]

Most catalysts for solution processes are either completely soluble or pseudo-homogeneous all their catalyst components are introduced into the reactor as Hquids but produce soHd catalysts when combined. The early Du Pont process employed a three-component catalyst consisting of titanium tetrachloride, vanadium oxytrichloride, and triisobutjlalurninum (80,81), whereas Dow used a mixture of titanium tetrachloride and triisobutylalurninum modified with ammonia (86,87). Because processes are intrinsically suitable for the use of soluble catalysts, they were the first to accommodate highly active metallocene catalysts. Other suitable catalyst systems include heterogeneous catalysts (such as chromium-based catalysts) as well as supported and unsupported Ziegler catalysts (88—90). [Pg.387]

Similar to IFP s Dimersol process, the Alphabutol process uses a Ziegler-Natta type soluble catalyst based on a titanium complex, with triethyl aluminum as a co-catalyst. This soluble catalyst system avoids the isomerization of 1-butene to 2-butene and thus eliminates the need for removing the isomers from the 1-butene. The process is composed of four sections reaction, co-catalyst injection, catalyst removal, and distillation. Reaction takes place at 50—55°C and 2.4—2.8 MPa (350—400 psig) for 5—6 h. The catalyst is continuously fed to the reactor ethylene conversion is about 80—85% per pass with a selectivity to 1-butene of 93%. The catalyst is removed by vaporizing Hquid withdrawn from the reactor in two steps classical exchanger and thin-film evaporator. The purity of the butene produced with this technology is 99.90%. IFP has Hcensed this technology in areas where there is no local supply of 1-butene from other sources, such as Saudi Arabia and the Far East. [Pg.440]

Extensive efforts have been made to develop catalyst systems to control the stereochemistry, addition site, and other properties of the final polymers. Among the most prominant ones are transition metal-based catalysts including Ziegler or Ziegler-Natta type catalysts. The metals most frequentiy studied are Ti (203,204), Mo (205), Co (206-208), Cr (206-208), Ni (209,210), V (205), Nd (211-215), and other lanthanides (216). Of these, Ti, Co, and Ni complexes have been used commercially. It has long been recognized that by varying the catalyst compositions, the trans/cis ratio for 1,4-additions can be controlled quite selectively (204). Catalysts have also been developed to control the ratio of 1,4- to 1,2-additions within the polymers (203). [Pg.346]

Erom 1955—1975, the Ziegler-Natta catalyst (91), which is titanium trichloride used in combination with diethylaluminum chloride, was the catalyst system for propylene polymerization. However, its low activity, which is less than 1000 g polymer/g catalyst in most cases, and low selectivity (ca 90% to isotactic polymer) required polypropylene manufacturers to purify the reactor product by washing out spent catalyst residues and removing unwanted atactic polymer by solvent extraction. These operations added significantly to the cost of pre-1980 polypropylene. [Pg.203]

As a result of the work of Ziegler in Germany, Natta in Italy and Pease and Roedel in the United States, the process of co-ordination polymerisation, a process related to ionic polymerisation, became of significance in the late 1950s. This process is today used in the commercial manufacture of polypropylene and polyethylene and has also been used in the laboratory for the manufacture of many novel polymers. In principle the catalyst system used governs the way in which a monomer and a growing chain approach each other and because of this it is possible to produce stereoregular polymers. [Pg.37]

Factors affecting laboratory polymerisation of the monomer have been discussed" and these indicate that a Ziegler-Natta catalyst system of violet TiCl3 and diethyl aluminium chloride should be used to react the monomer in a hydrocarbon diluent at atmospheric pressure and at 30-60°C. One of the aims is to get a relatively coarse slurry from which may be washed foreign material such as catalyst residues, using for example methyl alcohol. For commercial materials these washed polymers are then dried and compounded with an antioxidant and if required other additives such as pigments. [Pg.270]

Polybutadiene was first prepared in the early years of the 20th century by such methods as sodium-catalysed polymerisation of butadiene. However, the polymers produced by these methods and also by the later free-radical emulsion polymerisation techniques did not possess the properties which made them desirable rubbers. With the development of the Ziegler-Natta catalyst systems in the 1950s, it was possible to produce polymers with a controlled stereo regularity, some of which had useful properties as elastomers. [Pg.290]

Polymers containing 90-98% of a c 5-1,4-structure can be produced using Ziegler-Natta catalyst systems based on titanium, cobalt or nickel compounds in conjuction with reducing agents such as aluminium alkyls or alkyl halides. Useful rubbers may also be obtained by using lithium alkyl catalysts but in which the cis content is as low as 44%. [Pg.290]

The polyalkenamers are usually prepared by means of a Ziegler-Natta catalyst system. For example fran.v-polypentenamer may be obtained from cyclopentene... [Pg.304]

Attempts to produce coplymers of ethylene and styrene by free radical and by conventional Ziegler-Natta catalysts systems have, over the years, not proved successful. However, in 1998 Dow announced novel polymers using a metallocene process with the intention of commercial polymerisation using a 23 000t.p.a. capacity plant starting in 1999. [Pg.308]

Following their introduction in 1953, Ziegler-Natta catalysts revolutionized the field of polymer chemistry because of two advantages the resultant polymers are linear, with practically no chain branching, and they are stereochemical ly controllable. Isotactic, syndiotactic, and atactic forms can all be produced, depending on the catalyst system used. [Pg.1209]

In contrast to the processes of Ethyl and of Chevron/Gulf, which use Ziegler catalyst in the oligomerization of the ethylenes, Shell uses a self-developed catalyst system consisting of, for example, a nickel salt, a rm-organophosphine group, and a polar solvent such as 1,4-butanediol (3) [34,35] ... [Pg.50]

In comparison to the Ziegler catalyst, the use of the nickel catalyst system offers the following advantages [34] ... [Pg.50]


See other pages where Ziegler Catalyst Systems is mentioned: [Pg.791]    [Pg.387]    [Pg.207]    [Pg.809]    [Pg.453]    [Pg.182]    [Pg.24]    [Pg.387]    [Pg.233]    [Pg.791]    [Pg.387]    [Pg.207]    [Pg.809]    [Pg.453]    [Pg.182]    [Pg.24]    [Pg.387]    [Pg.233]    [Pg.356]    [Pg.367]    [Pg.383]    [Pg.397]    [Pg.398]    [Pg.407]    [Pg.410]    [Pg.411]    [Pg.411]    [Pg.411]    [Pg.413]    [Pg.430]    [Pg.506]    [Pg.38]    [Pg.211]    [Pg.248]    [Pg.327]    [Pg.161]    [Pg.287]    [Pg.431]    [Pg.331]   
See also in sourсe #XX -- [ Pg.105 ]




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Catalyst systems Ziegler-Natta catalysts

Ziegler catalyst

Ziegler systems

Ziegler-Natta catalyst system

Ziegler-Natta catalyst system structures

Ziegler-Natta catalysts heterogeneous systems

Ziegler-Natta catalysts metallocene-based systems

Ziegler-Natta catalysts titanium-aluminum systems

Ziegler-Natta olefin polymerization soluble catalyst systems

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