The invention relates to an efficient process for the preparation of isoolefin polymers such as polyisobutene or butyl rubber by polymerization of isobutene and optionally further monomers in the presence of an initiator system prepared by continuously contacting at least one boron or aluminium compound and at least one initiator.

A method of determining multimodal polyethylene quality comprising the steps of (a) providing a multimodal polyethylene resin sample; (b) determining, in any sequence, the following: that the multimodal polyethylene resin sample has a melt index within 30% of a target melt index; that the multimodal polyethylene resin sample has a density within 2.5% of a target density; that the multimodal polyethylene resin sample has a dynamic viscosity deviation (% MVD) from a target dynamic viscosity of less than about 100%; that the multimodal polyethylene resin sample has a weight average molecular weight (M.sub.w) deviation (% M.sub.wD) from a target M.sub.w of less than about 20%; and that the multimodal polyethylene resin sample has a gel permeation chromatography (GPC) curve profile deviation (% GPCD) from a target GPC curve profile of less than about 15%; and (c) responsive to step (b), designating the multimodal polyethylene resin sample as a high quality resin.

A method capable of stably performing continuous production of a propylene polymer with high productivity while reducing generation of agglomerates is described. In the method, a monomer(s) containing propylene is/are (co)polymerized in a presence of an olefin polymerization catalyst with a polymerization system containing two or more gas phase polymerization reactors or a polymerization system containing a liquid phase polymerization reactor(s) and a gas phase polymerization reactor(s) such that that the total number of liquid phase polymerization reactor(s) and gas phase polymerization reactor(s) is three or more. In at least one gas phase polymerization reactor, an average retention time τ.sub.G [hour] in the gas phase polymerization, an average particle diameter D.sub.pi [μm] of fed powder, and a total amount C.sub.o [wt %] of an ethylene-derived structural unit and C4-C12 α-olefin-derived structural units in a polymer in discharged powder are in a predetermined relationship.

A method capable of stably performing continuous production of a propylene polymer with high productivity while reducing generation of agglomerates is described. In the method, a monomer(s) containing propylene is/are (co)polymerized in a presence of an olefin polymerization catalyst with a polymerization system containing two or more gas phase polymerization reactors or a polymerization system containing a liquid phase polymerization reactor(s) and a gas phase polymerization reactor(s) such that that the total number of liquid phase polymerization reactor(s) and gas phase polymerization reactor(s) is three or more. In at least one gas phase polymerization reactor, an average retention time τ.sub.G [hour] in the gas phase polymerization, an average particle diameter D.sub.pi [μm] of fed powder, and a total amount C.sub.o [wt %] of an ethylene-derived structural unit and C4-C12 α-olefin-derived structural units in a polymer in discharged powder are in a predetermined relationship.

A method for evaluating long-term durability of a resin for piping is provided. Unlike the conventional FNCT evaluation method requiring a long period of time, the method disclosed herein is capable of predicting long-term durability of a resin for piping in a short time, by a simple calculation using a content of tie molecules, an entanglement molecular weight (M.sub.e) and a content of ultrahigh molecular weight components. In addition, the olefinic polymer is configured to have a predetermined relationship in relation to the content of tie molecules, the entanglement molecular weight (M.sub.e) and the content of ultrahigh molecular weight components, whereby the polymer of the present application can be used in the manufacture of a heating pipe requiring excellent long-term durability.

A method for producing a polyolefin with a wide molecular weight distribution can comprise: polymerizing one or more monomers in the presence of a catalyst system in a loop reactor to produce a polyolefin product having a polydispersity index of 2.5 to 8, wherein the loop reactor comprises two or more reactors in series, and wherein the loop reactor has a loop thermal gradient of 50° C. to 150° C. and/or a standard deviation of inter-component thermal gradients along the loop reactor of 10° C. to 50° C.

A method for setting conditions for use of a polymerization catalyst includes a step of acquiring a physical property value derived from remaining functional groups after maintaining a temperature of a composition including a polymerization-reactive compound and a predetermined amount of a polymerization catalyst, a step of calculating a remaining functional group ratio from the physical property value, a step of calculating a reaction rate constant based on a reaction rate equation from the remaining functional group ratio, a step of calculating an activation energy and a frequency factor from the reaction rate constant using an Arrhenius plot, a step of determining whether or not the activation energy satisfies a predetermined condition for the polymerization catalyst, an step of setting an approximation equation from the frequency factor, and a step of setting an addition range with respect to the polymerization-reactive compound.

Provided are an ethylene-vinyl acetate copolymer having a high degree of crosslinking by controlling a temperature difference in an autoclave reactor and an input ratio of an initiator during polymerization, even though a reduced amount of a crosslinking agent is used, and a preparation method thereof.

A method for predicting physical properties of a polyethylene resin is provided, which can reliably predict a proper charging ratio of a crosslinking agent in the production process of a low density crosslinked polyethylene resin, and the physical properties of the polyethylene resin achieved therefrom. A method for producing a polyethylene resin by applying the same method is also provided.

According to an embodiment of the present invention, provided is a process for polymerizing molecular weight—adjustable polymer, comprising: a reactant supply step of supplying a gaseous monomer, a surfactant, and an initiator; a polymerization reaction step of performing a polymerization reaction in which the monomer, the surfactant, and the initiator participate; and a product discharging step of discharging the polymer compound produced by the polymerization reaction, wherein the flow rate of the supplied initiator is inversely proportional to the molecular weight of the polymer compound, and the molecular weight of the polymer compound produced by the polymerization reaction is adjusted by controlling the flow rate of the initiator.