Lg Chem, Ltd

Jungmin Sohn

Hyemin Lee

Tae Young Won

Chang Hun Han

Kwangin Shin

Junwye Lee

Seongbeom Heo

Minsu Kim

Yeonsoo Kim

Jihye Ryu

According to the method for preparation of a super absorbent polymer according to the present disclosure, fine particles present in the prepared super absorbent polymer are removed, thereby solving a dispersion problem of the fine particles and a problem of reduction in the physical properties of the super absorbent polymer.

Method for preparation of super absorbent polymer

The present disclosure relates to a preparation method of a super absorbent polymer capable of preparing a super absorbent polymer exhibiting an improved absorption rate while reducing an amount of a blowing agent used. The preparation method of a super absorbent polymer includes: preparing a monomer mixture including a water-soluble ethylene-based unsaturated monomer having at least partially neutralized acidic groups and an internal cross-linking agent; adjusting a dynamic pressure applied to the monomer mixture being transferred to 140 Pa or more by controlling a transfer rate while transferring the monomer mixture to a polymerization reactor; cross-linking and polymerizing the monomer mixture transferred to the polymerization reactor to form a hydrogel polymer; drying, pulverizing and classifying the hydrogel polymer to form a base resin powder; and further cross-linking a surface of the base resin powder in the presence of a surface cross-linking agent to form a surface cross-linked layer.

Preparation method of super absorbent polymer

The present disclosure relates to a super absorbent polymer and a preparation method of the same, which not only has excellent basic absorption performance, but also exhibits an improved absorption rate, and the like. The super absorbent polymer includes a base resin powder containing a first cross-linked polymer of a water-soluble ethylene-based unsaturated monomer having at least partially neutralized acidic groups; and a surface cross-linked layer containing a second cross-linked polymer in which the first cross-linked polymer is additionally cross-linked by a surface cross-linking agent on the base resin powder, wherein the super absorbent polymer contains less than 9.9% by number of super absorbent polymer particles having an aspect ratio, which is defined as shortest diameter/longest diameter of each super absorbent polymer particle, of less than 0.5, a vortex time is 5 to 55 seconds by a vortex method, and a surface tension is 50 to 80 mN/m.

Super absorbent polymer and preparation method thereof

Provided are a superabsorbent polymer exhibiting more improved absorption rate and liquid permeability as well as excellent basic absorption performance, and a preparation method thereof. The superabsorbent polymer includes a base polymer powder including a crosslinked polymer of water-soluble ethylene-based unsaturated monomers having acidic groups which are at least partially neutralized; and a surface crosslinked layer which is formed on the base polymer powder and in which the base polymer powder is additionally crosslinked via a surface crosslinking agent, wherein the superabsorbent polymer includes 10% by number or more of superabsorbent polymer particles each particle having an aspect ratio of less than 0.5, the aspect ratio defined as the shortest diameter/the longest diameter of the superabsorbent polymer particle, and has SFC in a predetermined range.

Superabsorbent polymer and preparation method thereof

The present disclosure relates to a preparation method of a super absorbent polymer capable of improving absorption performance of the super absorbent polymer by adding a simple additive later. The preparation method includes the steps of: forming a hydrogel polymer by cross-linking and polymerizing a water-soluble ethylene-based unsaturated monomer having at least partially neutralized acidic groups in the presence of an internal cross-linking agent; drying, pulverizing and classifying the hydrogel polymer to form a base resin powder; forming a surface cross-linked layer by further cross-linking a surface of the base resin powder in the presence of a surface cross-linking agent, adding a monovalent to trivalent metal cation on the surface cross-linked base resin powder at a temperature of 25&#xb0; C. to 80&#xb0; C., and maintaining and aging the resulting metal cation-added product at a temperature of 40&#xb0; C. to 60&#xb0; C. for 10 to 30 minutes.

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Daejeon, South Korea

Jungmin Sohn