IP Library Granted Patent US 11,643,503
Granted Patent B2
US 11,643,503 · App. 16/925,780 · Granted May 9, 2023

Highly spherical polyamide microparticles and synthesis methods related thereto

Inventor: Hojjat Seyed Jamali (Mississauga, CA)
Assignee: XEROX CORPORATION
C08G69/46B29B2009/125
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Quick Facts
Patent No.
US 11,643,503
App. No.
16/925,780
Granted
May 9, 2023
Kind
B2
Abstract

A method of synthesizing polyamide microparticles may comprise: dehydrating and shearing a mixture comprising a matrix fluid, an emulsion stabilizer at about 0.01 wt % to about 50 wt % based on the weight of the matrix fluid, a solvent at about 13 wt % to about 75 wt % based on the weight of the matrix fluid, and a cyclic amide monomer at about 20 wt % to about 90 wt % based on the weight of the matrix fluid to yield an emulsion having a water content of about 1 wt % or less based on the total weight of the emulsion; adding a deprotonating agent to the emulsion at a concentration of about 0.01 wt % to about 1 wt % based on the weight of the matrix fluid; and contacting the emulsion with a polymerization initiator under conditions effective to polymerize the cyclic amide monomer into a plurality of polyamide microparticles.

Claims (32)

1. A method of synthesizing polyamide microparticles comprising:

dehydrating and shearing a mixture comprising a matrix fluid, an emulsion stabilizer, a solvent, and a cyclic amide monomer to yield an emulsion having a water content of about 1 wt % or less based on the total weight of the emulsion;

adding a deprotonating agent to the emulsion at a concentration of about 0.01 wt % to about 1 wt % based on the weight of the matrix fluid;

adding a polymerization initiator to the emulsion; and

polymerizing the cyclic amide monomer into a plurality of polyamide microparticles, wherein the polyamide microparticles have a diameter span of about 0.2 to about 10.

2. The method claim 1 , wherein the emulsion stabilizer is at about 0.01 wt % to about 50 wt % based on the weight of the matrix fluid.

3. The method claim 1 , wherein the solvent at about 13 wt % to about 75 wt % based on the weight of the matrix fluid.

4. The method claim 1 , wherein the cyclic amide monomer at about 20 wt % to about 90 wt % based on the weight of the matrix fluid.

5. The method claim 1 , wherein adding the deprotonating agent is before adding the polymerization initiator.

6. The method claim 1 , wherein adding the deprotonating agent is after adding the polymerization initiator.

7. The method claim 1 , wherein adding the deprotonating agent is at the same time as adding the polymerization initiator.

8. The method of claim 1 , wherein the cyclic amide monomer is selected from the group consisting of azeridinone, 2-azetidinone, 2-pyrrolidinone, 2-piperidinone, ε-caprolactam, 2-azacyclooctanone, 2-azacyclononanone, 2-azacyclodecanone, 2-azacycloundecanone, 2-aza-cyclododecanone, laurolactam, and any combination thereof.

9. The method of claim 1 , wherein the polyamide of the polyamide microparticles is selected from the group consisting of: polycaproamide, poly(hexamethylene succinamide), polyhexamethylene adipamide, polypentamethylene adipamide, polyhexamethylene sebacamide, polyundecaamide, polydodecaamide, polyhexamethylene terephthalamide, nylon 10.10, nylon 10.12, nylon 10.14, nylon 10.18, nylon 6.10, nylon 6.18, nylon 6.12, nylon 6.14, and any copolyamide thereof.

10. The method of claim 1 , wherein the matrix fluid comprises one selected from the group consisting of: polysiloxanes modified with fatty acids, polysiloxanes modified with fatty alcohols, polysiloxanes modified with polyoxy alkylenes, polydimethylsiloxane (PDMS), methylphenylpolysiloxane, an alkyl modified polydimethylsiloxane, an alkyl modified methylphenylpolysiloxane, an amino modified polydimethylsiloxane, an amino modified methylphenylpolysiloxane, a fluorine modified polydimethylsiloxane, a fluorine modified methylphenylpolysiloxane, a polyether modified polydimethylsiloxane, a polyether modified methylphenylpolysiloxane, silicone oil, fluorinated silicone oils, perfluorinated silicone oils, polyethylene glycols, paraffins, liquid petroleum jelly, vison oils, turtle oils, soya bean oils, perhydrosqualene, sweet almond oils, calophyllum oils, palm oils, parleam oils, grapeseed oils, sesame oils, maize oils, rapeseed oils, sunflower oils, cottonseed oils, apricot oils, castor oils, avocado oils, jojoba oils, olive oils, cereal germ oils, esters of lanolic acid, esters of oleic acid, esters of lauric acid, esters of stearic acid, fatty esters, higher fatty acids, and fatty alcohols, and any combination thereof.

11. The method of claim 1 , wherein the solvent has a boiling point greater than about 150° C.

12. The method of claim 1 , wherein the dehydrating is performed such that about 10% to about 15% of the solvent is distilled off during the dehydrating.

13. The method of claim 1 , wherein the polymerization initiator comprises one selected from the group consisting of: toluene diisocyanate (TDI), methylene diphenyl diisocyate (MDI), and any combination thereof.

14. The method of claim 1 , wherein the deprotonating agent comprises a Group I and Group II metal hydroxide, a Group I and Group II metal hydride, potassium methoxide, sodium methoxide, potassium ethoxide, sodium ethoxide, lithium ethoxide, potassium t-butoxide, sodium t-butoxide, lithium t-butoxide, sodium caprolactamates, ε-caprolactam magnesium bromides, sodium dicaprolactamato-bis-(2-methoxyethoxo)-aluminate, and any combination thereof.

15. The method of claim 1 further comprising:

washing the polyamide microparticles.

16. The method of claim 1 , wherein the polyamide microparticles have a D10 of about 0.5 μm to about 125 μm, a D50 of about 1 μm to about 200 μm, and a D90 of about 70 μm to about 300 μm, wherein D10<D50<D90.

17. The method of claim 1 , wherein the polyamide microparticles have a circularity of about 0.8 or greater.

18. A method of synthesizing polyamide microparticles comprising:

dehydrating and shearing a mixture comprising a matrix fluid, an emulsion stabilizer, a solvent, and a cyclic amide monomer to yield an emulsion having a water content of about 1 wt % or less based on the total weight of the emulsion;

adding a deprotonating agent to the emulsion at a concentration of about 0.01 wt % to about 1 wt % based on the weight of the matrix fluid;

adding a polymerization initiator to the emulsion; and

polymerizing the cyclic amide monomer into a plurality of polyamide microparticles, wherein the polyamide microparticles have a D10 of about 0.5 μm to about 125 μm, a D50 of about 1 μm to about 200 μm, and a D90 of about 70 μm to about 300 μm, wherein D10<D50<D90.

19. A method of synthesizing polyamide microparticles comprising:

dehydrating and shearing a mixture comprising a matrix fluid, an emulsion stabilizer, a solvent, and a cyclic amide monomer to yield an emulsion having a water content of about 1 wt % or less based on the total weight of the emulsion;

adding a deprotonating agent to the emulsion at a concentration of about 0.01 wt % to about 1 wt % based on the weight of the matrix fluid;

adding a polymerization initiator to the emulsion; and

polymerizing the cyclic amide monomer into a plurality of polyamide microparticles, wherein the polyamide microparticles have a circularity of about 0.8 or greater.

Assignments (9)
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2020
From: JAMALI, HOJJAT SEYED
To: XEROX CORPORATION
Reel/Frame 053174/0673 →
Continuity (1)
Related Publication 20220010066A1 · Jan 13, 2022
Cited By (1)
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