Water-absorbent resin composition, absorbent material and absorbent article
US-2024424473-A1 · Dec 26, 2024 · US
US9873770B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9873770-B2 |
| Application number | US-201314434692-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 14, 2013 |
| Priority date | Jan 31, 2008 |
| Publication date | Jan 23, 2018 |
| Grant date | Jan 23, 2018 |
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Solid-state shear pulverization of semi-crystalline polymers and copolymers thereof and related methods for enhanced crystallization kinetics and physical/mechanical properties.
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We claim: 1. A method of affecting crystallization kinetics of a semi-crystalline homopolymer, said method comprising: providing a solid semi-crystalline homopolymer component, said homopolymer a single homopolymer comprising less than about 50% crystallinity; and applying a mechanical energy to said single homopolymer through solid-state shear pulverization in the presence of cooling at least partially sufficient to maintain said homopolymer in a solid state during said pulverization, said pulverization at least partially sufficient to induce at least one of polymer scission and indigenous nucleation sites within said homopolymer, whereby said affected crystallization kinetic effect is selected from at least one of increased onset crystallization temperature and reduced isothermal crystallization half-time. 2. The method of claim 1 wherein said single homopolymer is selected from polyesters, polyolefins and polyamides. 3. A method of affecting crystallization kinetics of a semi-crystalline homopolymer, said method comprising: providing a solid semi-crystalline homopolymer component, said homopolymer a single homopolymer comprising less than about 50% crystallinity; and applying a mechanical energy to said single homopolymer through solid-state shear pulverization in the presence of cooling at least partially sufficient to maintain said homopolymer in a solid state during said pulverization, said pulverization at least partially sufficient to induce at least one of an increased crystallization temperature and reduced isothermal crystallization half-time of said single homopolymer as compared to said single homopolymer absent shear pulverization. 4. The method of claim 3 wherein increasing said applied energy increases at least one of crystallization onset temperature, peak temperature and endset temperature of said single homopolymer as compared to said single homopolymer absent shear pulverization. 5. The method of claim 3 wherein increasing said applied energy decreases said crystallization half-time of said single homopolymer as compared to said single homopolymer absent shear pulverization. 6. The method of claim 3 wherein said single homopolymer is selected from polyesters, polyolefins and polyamides. 7. The method of claim 3 substantially absent at least one of a nucleating agent and a filler component. 8. A method of using solid-state shear pulverization to affect crystallization kinetics of a semi-crystalline homopolymer, said method comprising: providing a solid semi-crystalline homopolymer component, said homopolymer component a single homopolymer comprising less than about 50% crystallinity; introducing said single homopolymer into a solid-state shear pulverization apparatus, said apparatus comprising a cooling component at least partially sufficient to maintain said homopolymer in a solid state; shear pulverizing said single homopolymer, said pulverization at least partially efficient to affect at least one of a crystallization temperature and isothermal crystallization half-time of said single homopolymer, and said pulverization substantially absent at least one of a nucleating agent and a filler component; and discharging said shear pulverized single homopolymer from said apparatus. 9. The method of claim 8 wherein said homopolymer is selected from polyesters, polyolefins and polyamides. 10. The method of claim 9 wherein said pulverization increases at least one of crystallization onset temperature, peak temperature and endset temperature of said single homopolymer as compared to said single homopolymer absent shear pulverization. 11. The method of claim 9 wherein said pulverization decreases said crystallization half-time of said single homopolymer as compared to said single homopolymer absent shear pulverization.
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