Abstract:
High impact polystyrene having a predominant core-shell morphology is made by polymerizing styrene in the presence of polybutadiene using toluene as a solvent. The thermoplastic polymer composition is characterized by a continuous phase of polystyrene containing dispersed graft copolymer particles having a core-shell structure with a polystyrene core occluded inside a polybutadiene shell. The styrene is desirably batch polymerized using styrene/toluene mixtures of about 70:30 by weight in the presence of from about 9 to about 15 weight percent polybutadiene while flashing off the toluene solvent.
Abstract:
A dual reactor process for the solution (co)polymerization of ethylene uses a catalyst having a phosphinimine ligand in each of the two reactors. In a preferred embodiment, the two reactors are operated at different temperatures and/or with different cocatalyst systems (such as “alumoxanes” and “ionic activators”) for the preparation of linear low density polyethylene (“LLPDE”) having a broad molecular weight distribution. Certain LLDPE polymers of this invention have an outstanding balance of physical properties (high dart impact strength and tear strength) excellent optical properties and excellent processability.
Abstract:
At least one single-stage or multistage stirrer which produces not only a tangential flow component but also an axial flow field is used in a stirred-vessel reactor in connection with the preparation of polymers by liquid phase polymerization.
Abstract:
A process for producing polyethylene having improved crack resistance, the process comprising copolymerizing ethylene and an alpha-olefinic comonomer comprising from 3 to 8 carbon atoms, in the presence of a chromium-based catalyst in a first reactor, feeding the polyethylene copolymer thereby produced and the chromium-based catalyst to a second reactor, and in the second reactor copolymerizing ethylene and an alpha-olefinic comonomer comprising from 3 to 8 carbon atoms, in the presence of the chromium-based catalyst thereby to produce a second polyethylene product, the first and second polyethylene products forming a combined polyethylene having a monomodal molecular weight distribution.
Abstract:
The present invention is to provide a production method of chemical reactive substances with stable quality by which solidification, gel formation, and the resulting blockade within material injection nozzles are prevented, and contamination of a reaction system with the gelled matter is prevented, as well as occurrence of problems on a production process due to the gelled matter is suppressed, when the chemical reactive substances are produced by injecting the liquid materials containing reactive substances having unsaturated double bonds into the reaction vessel through the material injection nozzles of the reaction vessel. The present invention is a production method of a chemical reactive substance which comprises injecting a liquid material containing a reactive substance having an unsaturated double bond into a reaction vessel through a material injection nozzle of said reaction vessel and causing a reaction at a reaction temperature of not less than 50° C., said production method of the chemical reactive substance including a step of removing at least a part of residual liquid remained in the material injection nozzle from inside of the material injection nozzle.
Abstract:
A process for preparing polypropylene-b-poly(ethylene-co-propylene) by the use of a tubular continuous polymerizer in the presence of an olefin-polymerizing catalyst comprising a solid catalyst component (1) composed of titanium and halogen; an organosilicon compound (2); and, if necessary, at least one electron-donating compound (3) selected from the group consisting of organosilicon compounds represented by the general formula: RnSi(OR′)4−n (wherein R and R′ are each independently a C1-C10 hydrocarbon group; and n is an integer of 1 to 3) and nitrogenous heterocyclic compounds, wherein the solid catalyst component (1) is preliminarily brought into contact with the organosilicon compound (2) in the presence of the electron-donating compound (3), and then a polypropylene segment is formed through polymerization, followed by formation of a poly(ethylene-co-propylene) segment at the end of the polypropylene segment through polymerization. The process enables efficient preparation of the polymer with a reduced content of inorganic contaminants, even when the polymer is one having a weight-average molecular weight of as high as 100,000 or more.
Abstract:
A dual reactor process for the solution and (co)polymerization of ethylene uses two different types of catalysts in the two reactors. A catalyst having a phosphinimine ligand is used in the first reactor. A Ziegler Natta catalyst is used in the second reactor. The process of this invention is comparatively easy to control and may be used to produce polyethylene products having a broad molecular weight distribution. Linear low density produced according to this invention is well suited for the manufacture of molded goods and plastic films.
Abstract:
Ethylene propylene copolymers, substantially free of diene, are described. The copolymers will have a uniform distribution of both tacticity and comonomer between copolymer chains. Further, the copolymers will exhibit a statistically insignificant intramolecular difference of tacticity. The copolymers are made in the presence of a metallocene catalyst.
Abstract:
Polyisobutene is prepared by cationic polymerization of isobutene and/or isobutene-containing hydrocarbons in the liquid phase in the presence of a complex of BF3 and at least one cocatalyst which is preferably chosen from oxygen-containing compounds, the BF3/cocatalyst complex being produced in situ by adding BF3 and cocatalyst to a reaction stream, wherein BF3 and oxygen-containing cocatalyst are added to the reaction stream via a common binary nozzle comprising an outlet for BF3 and an outlet for the oxygen-containing cocatalyst. The invention also describes a binary nozzle having a centrally arranged outlet for the catalyst.
Abstract:
Continuous anionic polymerization and melt-spinning of a polycaprolactam includes forming a reaction mixture by bringing at least two streams of liquid caprolactam respectively containing a polymerization initiator and co-initiator into contact with one another, and then subjecting the reaction mixture to anionic polymerization reaction conditions to obtain a molten polycaprolactam. The molten polycaprolactam is the directly (i.e., without intermediate solidification) transferred to, and extruded through, a fiber-forming orifice of a spinneret to form a fiber thereof. One exemplary system to achieve such continuous anionic polymerization and melt-spinning of polycaprolactam includes a mixer for receiving and mixing at least two streams of liquid caprolactam respectively containing a polymerization initiator and co-initiator, and a reactor and melt-spinning apparatus downstream of the mixer. The reactor and melt-spinning apparatus most preferably is formed of multiple plates which establish a reactor zone having a flow path for the reaction mixture which is sized and configured to achieve a predetermined residence time of the reaction mixture therein, and a temperature control zone in thermal communication with the reactor plate for controlling the temperature of the reaction plate to achieve anionic polymerization reaction conditions while the reaction mixture is flowing along the defined flow path therein to obtain the molten polycaprolactam. A spinneret zone downstream of the reactor zone thus receives the molten polycaprolactam directly and forms a fiber therefrom by extruding it through the spinneret's fiber-spinning orifice.