IP Library Granted Patent US 7,303,794
Granted Patent B2
US 7,303,794 · App. 10/813,772 · Granted Dec 4, 2007

Ink jet recording paper

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Quick Facts
Patent No.
US 7,303,794
App. No.
10/813,772
Granted
Dec 4, 2007
Kind
B2
Abstract

A thermal ink jet recording paper, incorporating dewatered and milled precipitated calcium carbonate (“PCC”) is disclosed. Precipitated calcium carbonate is dewatered and milled in the presence of an amphoteric or anionic dispersant to produce a high solids PCC composition. When used in coating formulations the PCC has a surface morphology and chemistry that enhances the printability of ink jet paper. Ink jet recording paper incorporating the PCC of the present invention has reduced ink feathering and spreading as well as improved optical density, dry time, and water fastness.

Claims (36)

1. A method for producing a precipitated calcium carbonate for ink jet recording paper comprising:

a) admixing calcium oxide with water to produce a calcium hydroxide slurry;

b) admixing a first amount of an organophosphonate followed by adding aluminum sulfate to the calcium hydroxide slurry;

c) introducing carbon dioxide to the calcium hydroxide slurry to produce a precipitated calcium carbonate slurry;

d) adding a second amount of organophosphonate to the precipitated calcium carbonate slurry;

e) admixing phosphoric acid to the precipitated calcium carbonate slurry;

f) screening and dewatering the calcium carbonate slurry; and

g) milling the screened and dewatered precipitated calcium carbonate in the presence of an amphoteric or anionic dispersant after step (d), to produce a precipitated calcium carbonate product.

2. The method of claim 1 wherein the first organophosphonate is selected from the group consisting of nitrilo-tris-(methylene phosphonic acid), ethylenediaminetetra (methylene phosphonic acid), diethylenetriaminepenta (methylene phosphonic acid), hydroxy ethane-1,1-diphosphonic acid, ethanolamine, ethanolamine bis-(methylenephosphonic acid), N-dimethylene phosphonic acid, and hexamethylenediaminetetra (methylene phosphonic acid).

3. The method of claim 1 wherein the first amount of the organophosphonate is employed at a level of from about 0.04 percent by weight calcium hydroxide slurry to about 0.15 percent by weight calcium hydroxide slurry and wherein the aluminum sulfate is from about 2.5 percent by weight calcium hydroxide slurry to about 4.5 percent by weight calcium hydroxide slurry.

4. The method of claim 1 wherein the first organophosphonate is ethanolamine bis-(methylenephosphonic acid).

5. The method of claim 1 wherein the second organophosphonate is employed at a level of from about 0.50 percent weight PCC slurry to about 1.0 percent weight PCC slurry.

6. The method of claim 1 wherein the second organophosphonate is ethanolamine bis-(methylenephosphonic acid).

7. The method of claim 1 wherein the amphoteric dispersant is selected from the group consisting of sodium salts of co-polymers of acrylic acid and diallyldimethylammonium chloride.

8. The method of claim 7 wherein the amphoteric dispersant is employed at a level of from about 1.0 percent active dispersant by weight PCC to about 5.0 percent active dispersant by weight PCC.

9. The method of claim 7 wherein the amphoteric dispersant has a molecular weight ranging from about 2000 to about 10000.

10. The method of claim 1 wherein the anionic dispersant is from the group consisting of sodium polyacrylates and copolymers of acrylic maleic acids.

11. The method of claim 1 wherein the anionic dispersant is employed at a level of from about 1.0 percent active dispersant by weight PCC to about 5.0 percent active dispersant by weight PCC.

12. The method of claim 1 wherein the anionic dispersant has a molecular weight ranging from about 2000 to about 10000.

13. The method of claim 1 wherein the PCC produced is from about 25 percent solids to about 65 percent solids concentration viscosity of from about 500 centipoise to about 1000 centipoise specific surface area of from about 60 m 2 /g to about 100 m 2 /g and surface charge of from about −(negative) 30 millivolt (mV) to about +5 mV.

14. A method for producing a precipitated calcium carbonate for ink jet recording paper comprising:

a) admixing calcium oxide with water to produce a calcium hydroxide slurry;

b) admixing a first amount of an organophosphonate followed by adding aluminum sulfate to the calcium hydroxide slurry;

c) introducing carbon dioxide to the calcium hydroxide slurry to produce a precipitated calcium carbonate slurry;

d) adding a second amount of organophosphonate to the precipitated calcium carbonate slurry;

e) admixing phosphoric acid to the precipitated calcium carbonate slurry;

f) screening and dewatering the calcium carbonate slurry;

g) milling the screened and dewatered precipitated calcium carbonate in the presence of an amphoteric or anionic dispersant after step (d), to produce a precipitated calcium carbonate product; and,

h) coating at least one side of a paper base stock with a coating formulation comprising the milled precipitated calcium carbonate and binder to form the ink jet recording paper.

15. A method according to claim 1 wherein the milled PCC is used in ink jet coating formulations for paperboard transparency, fabric, and tee-shirt iron-ons.

16. The method of claim 1 wherein the amphoteric dispersant is selected from the group consisting of sodium salts of co-polymers of acrylic acid and methyl chloride quaternaryamine of dimethylaminoethylacrylate.

17. The method of claim 16 wherein the amphoteric dispersant is employed at a level of from about 1.0 percent active dispersant by weight PCC to about 5.0 percent active dispersant by weight PCC.

18. The method of claim 16 wherein the amphoteric dispersant has a molecular weight ranging from about 2000 to about 10000.

19. The method of claim 1 wherein the amphoteric dispersant is selected from the group consisting of an acrylic acid and a diallyldimethylammonium chloride quaternaryamine copolymer.

20. The method of claim 19 wherein the amphoteric dispersant is employed at a level of from about 1.0 percent active dispersant by weight PCC to about 5.0 percent active dispersant by weight PCC.

21. The method of claim 19 wherein the amphoteric dispersant has a molecular weight ranging from about 2000 to about 10000.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR NAME PREVIOUSLY RECORDED ON REEL 032908 FRAME 0946. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded May 19, 2014
From: MINERALS TECHNOLOGIES INC.; SPECIALTY MINERALS (MICHIGAN) INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 032922/0127 →
SECURITY INTEREST Recorded May 15, 2014
From: MINERAL TECHNOLOGIES INC.; SPECIALTY MINERALS (MICHIGAN) INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 032908/0946 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2004
From: SUPERKA, ANNMARIE; ROTH, KEVIN JAY
To: SPECIALTY MINERALS (MICHIGAN) INC.
Reel/Frame 015171/0949 →