US20040108082A1

US20040108082A1 - Filler-fiber composite

Info

Publication number: US20040108082A1
Application number: US10/314,730
Authority: US
Inventors: Geoffrey Hughes
Original assignee: Specialty Minerals Michigan Inc
Current assignee: Specialty Minerals Michigan Inc
Priority date: 2002-12-09
Filing date: 2002-12-09
Publication date: 2004-06-10
Also published as: NO20053287L; AU2003294561A1; WO2004053228A3; WO2004053228A2; BR0317093A; AR042329A1; TW200508457A; CL2003002530A1; RU2005121563A; ZA200504337B; JP2006509120A; EP1579068A2; CN1723316A; CA2538371A1; KR20040050052A

Abstract

The present invention relates to a filler-fiber composite, a process for its production, the use of such in the manufacture of paper or paperboard products and to paper produced therefrom. More particularly the invention relates to a filler-fiber composite in which the morphology and particle size of the mineral filler are established prior to the development of the bond to the fiber. Even more particularly, the present invention relates to a PCC filler-fiber composite, wherein the desired optical and physical properties of the paper produced therefrom are realized.

Description

FIELD OF THE INVENTION

1. Background of the Invention

Loading particulate fillers such as calcium carbonate, talc and clay on fibers for the subsequent manufacture of paper and paper products continues to be a challenge. A number of methods, having some degree of success, have been used to address this issue. To insure that fillers remain with or within the fiber web, retention aids have been used, direct precipitation onto the fibers have been used, a method to attach the filler directly to the surface of the fiber have been used, mixing the fiber and the filler have been used, precipitation within never dried pulp have been used, a method for filling the cellulosic fiber have been used, high shear mixing have been used, fiberous material and calcium carbonate have been reacted with carbon dioxide in a closed pressurized container, fillers have been trapped by mechanical bonding, cationically charged polymers have been used and pulp fiber lumen loaded with calcium carbonate have all been used to retain filler in fiber for subsequent use in paper. Most of the methods for fiber retention are both expensive and ineffective.

Therefore, what is needed is a filler fiber composite and a method for producing the same that is both effective in retaining the filler and inexpensive for the paper maker to utilize.

Therefore, an object of the present invention is to produce a filler-fiber composite. Another object of the present invention is to provide a method for producing a filler-fiber composite. While another object of the present invention is to produce a filler-fiber composite that maintains physical properties such as tensile strength, breaking length and internal bond strength. Still a further object of the present invention is to produce a filler-fiber composite that maintains optical properties such as ISO opacity and pigment scatter. While still a further object of the present invention is to provide a filler-fiber composite that is particularly useful in paper and paperboard products.

2. Related Art

U.S. Pat. No. 6,156,118 teaches mixing a calcium carbonate filler with noil fibers in a size of P50 or finer.

U.S. Pat. No. 5,096,539 teaches in-situ precipitation of an inorganic filler with never dried pulp.

U.S. Pat. No. 5,223,090 teaches a method for loading cellulosic fiber using high shear mixing of crumb pulp during carbon dioxide reaction.

U.S. Pat. No. 5,665,205 teaches a method for combining a fiber pulp slurry and an alkaline salt slurry in the contact zone of a reactor and immediately contacting the slurry with carbon dioxide and mixing so as to precipitate filler onto secondary pulp fibers.

U.S. Pat. No. 5,679,220 teaches a continuous process for in-situ deposition of fillers in papermaking fibers in a flow stream in which shear is applied to the gaseous phase to complete the conversion of calcium hydroxide to calcium carbonate immediately.

U.S. Pat. No. 5,122,230 teaches process for modifying hydrophilic fibers with a substantially water insoluble inorganic substance in-situ precipitation.

U.S. Pat. No. 5,733,461 teaches a method for recovery and use of fines present in a waste water stream produced in a paper manufacturing process.

U.S. Pat. No. 5,731,080 teaches in-situ precipitation wherein the majority of a calcium carbonate trap the microfiber by reliable and non-reliable mechanical bonding without binders or retention aids.

U.S. Pat. No. 5,928,470 teaches method of making metal oxide or metal hydroxide-modified cellulosic pulp.

U.S. Pat. No. 6,235,150 teaches a method of producing a pulp fiber lumen loaded with calcium carbonate having a particle size of 0.4 microns to 1.5 microns.

The problem of insuring that filler materials, such as calcium carbonate, ground calcium carbonate, clay and talc, remain within fibers that are ultimately to be used in paper has been subjected to a number of proofs. However, none of the prior related art discloses a filler fiber composite where the morphology of the filler is predetermined prior to introducing fibers, a method for its production nor its use in paper or paper products.

SUMMARY OF THE INVENTION

The present invention relates to a filler-fiber composite including feeding slake containing seed to a first stage reactor, reacting the slake containing seed in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry, reacting the first partially converted calcium hydroxide calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide to produce a second partially converted calcium hydroxide calcium carbonate slurry and reacting the second partially converted calcium hydroxide calcium carbonate slurry in a third stage reactor in the presence of carbon dioxide and fibers to produce a filler-fiber composite.

In another aspect, the present invention relates to a filler-fiber composite including feeding slake containing seed to a first stage reactor, reacting the slake containing seed in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry and reacting the first partially converted calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide and fibers to produce a filler-fiber composite.

In a further aspect, the present invention relates to a filler-fiber composite including feeding slake containing citric acid to a first stage reactor, reacting the slake containing citric acid in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry, reacting the first partially converted calcium hydroxide calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide to produce a second partially converted calcium hydroxide calcium carbonate slurry, and reacting the second partially converted calcium hydroxide calcium carbonate slurry in a third stage reactor in the presence of carbon dioxide and fibers to produce a filler-fiber composite.

In yet a further aspect, the present invention relates to a filler-fiber composite Including feeding slake containing citric acid to a first stage reactor, reacting the slake containing citric acid in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry, taking a first portion of the partially converted calcium hydroxide calcium carbonate slurry adding fibers and reacting such in a second stage reactor in the presence of carbon dioxide to produce a calcium carbonate fiber composite to serve as a heel and taking a second portion of the partially converted calcium hydroxide calcium carbonate slurry adding fibers and surfactant and reacting in the presence of CO ₂to produce a second partially converted Ca(OH)₂/CaCO₃/fiber material and reacting the second partially converted Ca(OH)₂/CaCO₃/fiber material in the presence of CO₂in a third stage reactor to produce a filler-fiber composite.

In still a further aspect, the present invention relates to a filler-fiber composite including feeding slake containing citric acid to a first stage reactor, reacting the slake containing citric acid in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry, taking a first portion of the partially converted calcium hydroxide calcium carbonate slurry adding fibers and reacting such in a second stage reactor in the presence of carbon dioxide to produce a calcium carbonate/fiber composite to serve as a heel and taking a second portion of the partially converted calcium hydroxide calcium carbonate slurry adding fibers and polyacrylamide and reacting in the presence of CO ₂to produce a second partially converted Ca(OH)₂/CaCO₃/fiber material and reacting the second partially converted Ca(OH)₂/CaCO₃/fiber material in the presence of CO₂in a third stage reactor to produce a filler-fiber composite.

In a final aspect, the present invention relates to a filler-fiber composite including feeding slake containing citric acid to a first stage reactor, reacting the slake containing citric acid in the first stage reactor in the presence of carbon dioxide to produce a CaCO ₃heel and adding slake containing sodium carbonate to the heel material of the first stage reactor in the presence of CO₂to produce a partially converted calcium hydroxide calcium carbonate slurry and reacting the partially converted calcium hydroxide calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide and fibers to produce a filler-fiber composite.

Fiber as used in the present invention is defined as fiber produced by refining (any pulp refiner

known in the pulp processing industry) cellulose and/or mechanical pulp fiber. The fibers are typically 0.1 to 2 microns in thickness and 10 to 400 microns in length and are additionally prepared according to U.S. Pat. No. 6,251,222, which is by this reference incorporated herein.

DETAILED DESCRIPTION OF THE INVENTION

Precipitation of PCC with Varying Morphologies

Continuous Flow Stir Tank Reactor (CFSTR)

Scalenohedral Morpholog

The first step in this process involves making a high reactive Ca(OH) ₂milk-of-lime slake and screening it at −325 mesh. This slake is then added to an agitated reactor, brought to a desired reaction temperature, 0.1 percent citric acid is added to the slake to inhibit aragonite formation, and reacted with CO₂gas. The reaction proceeds 10 percent to 40 percent of the way through at which point the reaction is stopped. This produces a partially converted Ca(OH)₂/CaCO₃slurry (approximately 20 percent solids by weight) which is then fed into a reaction vessel at a rate that matches CO₂gassing to maintain a given conductivity (ionic saturation) to produce a scalenohedral crystal. This reaction proceeds until stabilization of the process is achieved. The product made once stabilization is achieved (approximately 95 percent converted) is then mixed with diluted fibers (approximately 1.5 percent concentration) and water. This mixture is then reacted with CO₂gas to endpoint pH 7.0. The product manufactured using this method can contain from about 0.2 percent to about 99.8 percent scalenohedral PCC with respect to fibers at 3 percent to 5 percent total solids.

The product has a specific surface area from about 5 meters squared per gram to about 11 meters squared per gram; product solids from about 3 percent to about 5 percent and a PCC content from about 0.2 percent to about 99.8 percent, and is predominantly scalenohedral in morphology.

Aragonitic Morpholog

The first step in this process involves making a high reactive Ca (OH) ₂milk-of-lime slake and screened at −325 mesh. The concentration of this slake is approximately 15 percent by weight. This slake is then added to an agitated reactor, brought to a desired reaction temperature, from about 0.05 percent to about 0.04 percent additive is added to direct morphology and size, and reacted with CO₂gas. The reaction proceeds 10 percent to 40 percent of the way through at which point the reaction is stopped. This produces a partially converted Ca (OH)₂/CaCO₃slurry which is then fed into a reaction vessel at a rate that matches CO₂gassing to maintain a given conductivity (ionic saturation) to produce an acicular, aragonitic crystal. The reaction continues until process stabilization is achieved. The product made once stabilization is achieved, (approximately 95 percent calcium carbonate) is mixed with diluted fibers (approximately 1.5 percent concentration) and water. The calcium carbonate and fibers are then reacted with CO₂gas to an endpoint of pH 7.0. The product manufactured using this method contains from about 0.2 percent to about 99.8 percent aragonitic PCC with respect to the fibers at about 3 percent to about 5 percent total solids.

The product has a specific surface area of about 5 meters squared per gram to about 8 meters squared per gram; product solids from about 3 percent to about 5 percent by weight and a PCC content from about 0.2 percent to about 99.8 percent with respect to fibers and has a predominantly aragonitic morphology.

Rhombohedral Morphology

The first step in this process involves making a high reactive Ca (OH) ₂milk-of-lime slake which is screened at −325 mesh and has a concentration of approximately 20 percent by weight. 0.1 percent citric acid is added to inhibit aragonite formation. A portion of this slake is added to an agitated reactor, brought to a desired reaction temperature and carbonated with CO₂gas. The reaction proceeds to conductivity minimum producing a “heel”. A “heel” is defined as a fully converted calcium carbonate crystal with average particle size typically in the range of about 1 micron to about 2.5 micron with any crystal morphology. Sodium carbonate is added to the remainder of the slake not used in the manufacture of the “heel” material. This slake and CO₂is added to the “heel” material at a CO₂gassing rate to maintain a given conductivity (ionic saturation) to produce a rhombohedral crystal. The reaction is continued until process stabilization is achieved. Once stabilization is achieved, this product (approximately 90 percent to 95 percent converted) is mixed with diluted fibers (approximately 1.5 percent concentration) and water. Additional CO₂is added to an endpoint of pH 7.0. The product manufactured using this method contains from about 0.2 percent to about 99.8 percent rhombohedral PCC with respect to fibers and is about 3 percent to about 5 percent total solids.

The product has a specific surface area from about 5 meters squared per gram to about 8 meters squared per gram; product solids from about 3 percent to about 5 percent; and PCC content from about 0.2 percent to about 99.8 percent and has a predominantly rhombohedral morphology:

EXAMPLES

The following examples are intended to exemplify the invention and are not intended to limit the scope of the invention. [0037]

Example 1

Scalenohedral PCC [0038]
Reacted 15 liters of water with 3 kilogram CaO at 50 degrees Celsius producing a 20 percent by weight Ca(OH)[0039] ₂slake. The Ca(OH)₂slake was then screened at −325 mesh producing a screened slake that was transferred to a first 30-liter double jacketed stainless steel reaction vessel with an agitation of 615 revolutions per minute (rpm). 0.1 percent citric acid, by weight of total theoretical CaCO₃to be produced, was added to the screened slake in a 30-liter reaction vessel and the temperature of the contents brought to 40 degrees Celsius. Began addition of 20 percent CO₂gas in air (14.83 standard liter minute CO₂/59.30 standard liter minute air) to the 30-liter reaction vessel to produce a 2:1 Ca (OH)₂/CaCO₃slurry. At this point, CO₂gassing was stopped and the slurry was transferred to an agitated 20-liter storage vessel. 2 liters of the 2:1 Ca(OH)₂/CaCO₃slurry was transferred to a first 4-liter agitated (1250 rpm) stainless steel, double jacketed reaction vessel. The temperature was brought to 51 degrees Celsius and 20 percent CO₂gas in air (1.41 standard liter minute CO₂/5.64 standard liter minute air) was added to the first 4-liter reaction vessel until a pH of 7.0 was achieved producing a CaCO₃slurry. Once a pH 7.0 was achieved began addition of the 2:1 Ca(OH)₂/CaCO₃slurry of the 20-liter storage vessel to the first 4-liter reaction vessel while continuing to add 20 percent CO₂gas in air (1.41 standard liter minute CO₂/5.64 standard liter minute air) to the first 4-liter reaction vessel to maintain a conductivity of approximately 90 percent ionic saturation. The addition of Ca(OH)₂/CaCO₃slurry and CO₂to the first 4-liter reaction vessel was continued for approximately 12 hours until product physical properties remained essentially unchanged, producing a CaCO₃slurry that was approximately 98 percent converted. Transferred 0.18 liters of the 98 percent CaCO₃slurry to a second 4-liter agitated (1250 rpm), stainless steel, double jacketed reaction vessel, added 0.66 liters of 3.8 percent by dry weight cellulosic fibers and diluted to 1.5 percent consistency. This mixture of CaCO₃slurry and fiber was reacted with 20 percent CO₂in air (1.41 standard liter minute CO₂/5.64 standard liter minute air) to produce a CaCO₃filler-fiber composite. The calcium carbonate filler had a predominantly scalenohedral morphology.

Example 2

Aragonitic PCC [0040]
Reacted 10.5 liters of water with 2.1 kilograms CaO at 50 degrees Celsius producing a 15 percent by weight Ca(OH)[0041] ₂slake. The Ca(OH)₂slake was then screened at −325 mesh producing a screened slake that was transferred to a 30-liter double jacketed stainless steel reaction vessel with an agitation of 615rpm. Added 0.1 percent by weight of a high surface area (HSSA) aragonitic seed (surface area ˜40 meters squared per gram, approximately 25 percent solids) to the 30-liter reaction vessel and brought the temperature of the contents to 51 degrees Celsius. A “seed” is defined as a fully converted aragonitic crystal that has been endpointed and milled to a high specific surface area (i.e. greater than 30 meters squared per gram and typically a particle size of 0.1 to 0.4 microns). Began addition of 10 percent CO₂gas in air (5.24 standard liter minute CO₂/47.12 standard liter minute air) to the 30-liter stainless steel, double jacketed reaction vessel for a 15-minute period after which the CO₂concentration was increased to 20 percent in air (10.47 standard liter minute CO₂/41.89 standard liter minute air) for an additional 15 minutes producing a 2.3:1 Ca (OH)₂/CaCO₃slurry. At which time CO₂gassing was stopped. The 2.3:1 Ca(OH)₂/CaCO₃slurry was transferred to an agitated 20-liter storage vessel. Transferred 2 liters of the 2.3:1 Ca(OH)₂/CaCO₃slurry to a first 4-liter agitated, double jacketed stainless steel reaction vessel with agitation set at 1250rpm and the temperature was brought to 52 degrees Celsius. Began addition of 20 percent CO₂gas in air (1.00 standard liter minute CO₂/3.99 standard liter minute air) to the first 4-liter reaction vessel and the reaction was continued until a pH of 7.0 was achieved producing a 100 percent CaCO₃slurry. The temperature of the 100 percent CaCO₃slurry of the first 4-liter reaction vessel was brought to 63 degrees Celsius. Began addition of the 2.3:1 Ca(OH)₂/CaCO₃slurry of the 20-liter storage vessel to the first 4-liter reaction vessel while continuing to add 20 percent CO₂in air (1.00 standard liter minute CO₂/3.99 standard liter minute air) to the first 4-liter reaction vessel maintaining a conductivity of approximately 90 percent ionic saturation. Continued the reaction for approximately 9 hours until the physical properties of the resultant product remained essentially unchanged, producing a 98 percent by wt. CaCO₃slurry.
Transferred 0.35 liters of the 98 percent CaCO[0042] ₃slurry to a second 4-liter agitated (1250 rpm), stainless steel, double jacketed reaction vessel, added 0.66 liters of 3.8 percent by wt. cellulosic fiber and 1.0 liters water to the second 4-liter reactor producing a 1.5 percent by wt. CaCO₃/fiber mixture. Added an additional 20 percent CO₂in air (1.00 standard liter minute CO₂/3.99 standard liter minute air) to the second 4-liter reaction vessel until a pH of 7.0 was reached at which time the reaction was completed producing a CaCO₃/fiber composite. The composite consisted of approximately 75 percent aragonitic PCC to fiber.

Example 3

Rhombohedral PCC [0043]
Reacted 15 liters of water with 3 kilograms CaO at 50 degrees Celsius producing a 20 percent by weight Ca(OH)[0044] ₂slake. The Ca(OH)₂slake was screened at −325 mesh producing a screened slake that was transferred to an agitated 20-liter storage vessel. Transferred 2-liters of the screened slake from the 20-liter storage vessel to a first 4-liter agitated, stainless steel, double jacketed reaction vessel and began agitation at 1250 rpm. Added 0.03 percent citric acid by weight of theoretical CaCO₃to the first 4-liter reaction vessel and raised the temperature of the contents to 50 degrees Celsius. Added 20 percent CO₂gas in air (1.44 standard liter minute CO₂/5.77 standard liter minute air) to the first 4-liter reaction vessel until a pH of 7.0 was achieved producing a 100 percent CaCO₃slurry. To the screened slake in the 20-liter storage vessel, added a solution of 1.3 percent by weight of Na₂CO₃, based on theoretical yield of CaCO₃, producing a Ca(OH)₂/Na₂CO₃slake. Increased the temperature of the contents of the first 4-liter reaction vessel to approximately 68 degrees Celsius and began addition of the Ca(OH)₂/Na₂CO₃slake of the 20-liter storage vessel to the first 4-liter reaction vessel while continuing to add 20 percent CO₂in air (1.44 standard liter minute CO₂/5.77 standard liter minute air) to the first 4-liter reaction vessel maintaining a conductivity of approximately 50 percent ionic saturation. Addition of the Ca(OH)₂/Na₂CO₃slake and CO₂was continued for approximately 12 hours until physical properties of the resultant product remained essentially unchanged producing an approximate 98 percent by wt. CaCO₃slurry.
Transferred 0.22 liters of the 98 percent CaCO[0045] ₃slurry to a second 4-liter agitated (1250 rpm) dual jacketed, stainless steel reaction vessel and added 0.66 liters of 3.8 percent by weight cellulosic fiber and 1.0 liters water to the second 4-liter reactor producing a 1.5 percent by weight CaCO₃/fiber mixture. Added an additional 20 percent CO₂in air (1.44 standard liter minute CO₂/5.77 standard liter minute air) to the second 4-liter reaction vessel until a pH of 7.0 was reached at which time the reaction was completed producing an approximate 3.4 percent by wt CaCO₃/fiber composite. The calcium carbonate had a predominantly rhombohedral morphology.

Example 4

Scalenohedral—CFSTR [0046]
Reacted 15 liters of water with 3 kilograms CaO at 48 degrees Celsius to produce a Ca(OH)[0047] ₂slake, added an additional 6 liters of water producing a 20 percent by weight Ca(OH)₂slake. The 20 percent Ca(OH)₂slake was screened at −325 mesh and transferred to a 30-liter double jacketed, stainless steel reaction vessel with an agitation of 615 rpm. Added 0.015 percent citric acid, by weight of total theoretical CaCO₃to be produced, to the 30-liter reaction vessel and the temperature of the contents brought to 36 degrees Celsius. Began addition of 20 percent CO₂gas in air (13.72 standard liter minute CO₂/54.89 standard liter minute air) to the 30-liter reaction vessel to produce a 5:1 Ca(OH)₂/CaCO₃slurry. CO₂gassing was stopped and the Ca(OH)₂/CaCO₃slurry was transferred to an agitated 20-liter storage vessel.
In a 4-liter agitated storage vessel, combined 0.25 liters of the Ca(OH)[0048] ₂/CaCO₃slurry with 0.66 liters of 3.8 percent by weight fibers and with 1.09 liters of water making a Ca(OH)₂/CaCO₃/fiber material. Transferred 2 liters of the Ca(OH)₂/CaCO₃/fiber material to a 4-liter agitated (1250 revolutions per minute) reaction vessel and the temperature brought to 55 degrees Celsius and carbonated with 20 percent CO₂in air (1.30 standard liter minute CO₂/5.23 standard liter minute air) to a pH of 7.0 producing a CaCO₃/fiber composite. Prepared 16-liters of 1.5 percent by weight fibers and a separate 10-liter vessel of water. To the 4-liter reaction vessel began addition of the Ca(OH)₂/CaCO₃slurry of the 20-liter agitated storage vessel, along with the 1.5 percent consistency fiber mixture at 172.05 ml per minute, along with 31.21 ml per minute of additional water while maintaining the flow of CO₂gas (1.30 standard liter minute CO₂/5.23 standard liter minute air) at a rate to maintain conductivity of approximately 90 percent ionic saturation, while maintaining mass balance of approximately 4 percent to 5 percent total solids.
This reaction was continued until product physical properties remained essentially unchanged. Addition of material from the storage vessel was stopped while CO[0049] ₂addition was continued and the material in the 4-liter agitated reaction vessel was brought to a pH of 7.0 at which time CO₂addition was stopped producing a 2.2:1 CaCO₃/fiber composite with the CaCO₃having a well defined scalenohedral morphology.

Example 5

Scalenohedral CFSTR/Surfactant [0050]
Reacted 15 liters of water with 3 kilograms CaO at 48 degrees Celsius to produce a Ca(OH)[0051] ₂slake, added an additional 6 liters of water producing a 20 percent by weight Ca(OH)₂slake. The 20 percent Ca(OH)₂slake was screened at −325 mesh and transferred to a 30-liter reaction vessel (615revolutions per minute). Added 0.015 percent citric acid, by weight of total theoretical CaCO3 to be produced, to the 30-liter reaction vessel and the temperature of the contents brought to 35 degrees Celsius. Began addition of 20 percent CO₂gas in air (14.08 standard liter minute CO₂/56.30 standard liter minute air) to the 30-liter reaction vessel producing a 5:1 Ca(OH)₂/CaCO₃slurry. At this point, CO₂gassing was stopped and the Ca(OH)₂/CaCO₃slurry was transferred to a 20-liter agitated storage vessel.
In a 4-liter agitated storage vessel, combined 0.25 liters of the Ca(OH)[0052] ₂/CaCO₃slurry with 0.66 liters of 3.8 percent by weight fibers and with 1.09 liters of water making 2 liters of Ca(OH)₂/CaCO₃/fiber material.
Transferred 2 liters of the Ca(OH)[0053] ₂/CaCO₃/fiber material to a 4-liter stainless steel, double jacketed, agitated (1250 revolutions per minute) reaction vessel and the temperature was brought to 58 degrees Celsius. Reacted the Ca(OH)₂/CaCO₃/fiber material with 20 percent CO₂in air (1.30 standard liter minute CO₂/5.23 standard liter minute air) to a pH of 7.0.
At this point, prepared 16-liters of 1.5 percent by weight fibers (6.32 liters of fibers at 3.8 percent consistency and 9.68 liters of water) and a separate 10-liter vessel of water. Added 0.04 percent surfactant based on the volume of fibers at 1.5 percent consistency. The surfactant is Tergitol™ MIN-FOAM 2× which is available commercially from Union Carbide, 39 Old Ridgebury Road, Danbury, Conn. 06817. [0054]
Once a pH of 7.0 was achieved in the 4-liter reaction vessel, began addition of the remaining 5:1 Ca(OH)[0055] ₂/CaCO₃slurry from the 20-liter agitated storage vessel, with a flow of the 1.5 percent fiber mixture at 176.48 ml per minute and with 32.00 ml per minute water from the 10-liter vessel to the 4-liter reaction vessel while maintaining the flow of CO₂gas (1.30 standard liter minute CO₂/5.23 standard liter minute air) at a rate to maintain conductivity of approximately 90 percent ionic saturation, while maintaining mass balance of approximately 4 percent to 5 percent total solids. Continued addition of the material from the agitated storage vessel to the reaction vessel until product physical properties remained essentially unchanged. At which point, addition of material from the storage vessel was stopped while CO₂addition was continued to a pH of 7.0 at which time CO₂addition was stopped. This produced a 2.33:1 CaCO₃/fiber composite with the calcium carbonate having a well defined scalenohedral morphology.

Example 6

Scalenohedral CFSTR/Polyacrylamide [0056]
Reacted 15 liters of water with 3 kilograms CaO at 48 degrees Celsius producing a Ca(OH)[0057] ₂slake, added an additional 6 liters of water producing a 20 percent by weight Ca(OH)₂slake. The 20 percent Ca(OH)₂slake was then screened at −325 mesh producing a screened slake that was transferred to a 30-liter agitated (615 rpm) reaction vessel. Added 0.1 percent citric acid, by weight of total theoretical CaCO₃to be produced, to the 30-liter reaction vessel and the temperature of the contents brought to 50 degrees Celsius. Began addition of 20 percent CO₂gas in air (15.01 standard liter minute CO₂/60.06 standard liter minute air) to the 30-liter reaction vessel producing a 5:1 Ca(OH)₂/CaCO₃slurry. CO₂gassing was stopped and the slurry was transferred to a 20-liter agitated storage vessel. To a 4-liter agitated vessel added 0.31 liters of the Ca(OH)₂/CaCO₃slurry, 0.60 liters of fibers at 3.8 percent consistency and 1.09 liters of water to produce a Ca(OH)₂/CaCO₃/fiber material. 2 liters of the Ca(OH)₂/CaCO₃/fiber material was transferred to a 4-liter agitated (1250 revolutions per minute) reaction vessel and the temperature was brought to 51 degrees Celsius. Began addition of 20 percent CO₂in air (1.34 standard liter minute CO₂/5.34 standard liter minute air) until a pH of 7.0 was reached producing a CaCO₃/fiber composite.
At this point, prepared 16-liters of 1.5 percent by weight fibers (6.32 liters of fibers at 3.8 percent consistency and 9.68 liters of water) and a separate 10-liter vessel of water. Added 0.05 percent cationic polyacrylamide (Percol 292) based on the volume of fibers at 1.5 per cent consistency. Percol 292 is commercially available from Allied Colloids, 2301 Wikroy Road, Suffolk, Va. 23434. [0058]
Once a pH of 7.0 was achieved in the 4-liter reaction vessel, began addition of the remaining 5:1 Ca(OH)[0059] ₂/CaCO₃slurry from the 20-liter agitated storage vessel, with a flow of the 1.5 percent fiber mixture at 90 ml per minute, along with 48.5 ml per minute of additional water to the 4-liter agitated, double jacketed reaction vessel while maintaining the flow of CO₂gas (1.30 standard liter minute CO₂/5.23 standard liter minute air) at a rate to maintain conductivity level of approximately 90 percent ionic saturation, and maintain mass balance of the reaction to maintain product concentration at approximately 4 percent to 5 percent solids. Continued addition of the material from the agitated storage vessel to the reaction vessel until product physical properties remained essentially unchanged. Addition of material from the 20-liter storage vessel was stopped while CO₂addition was continued until a pH of 7.0 was reached at which time CO₂addition was stopped producing a 3.34:1 CaCO₃/fiber composite with the PCC having a well defined scalenohedral morphology.
The control fiber of the present invention was refined at the Empire State Paper Research Institute (ESPRI) using an Escher-Wyss (conical) refiner to an 80° SR (freeness). Measured by a fiber quality analyzer (using arithmatic means) the control fiber measured 200-400 microns [0060]
How Control Filler-Fiber was Made [0061]

Produce a 15% solids slake and mix with fibers (˜1.5% consistency) React in the presence of CO ₂to endpoint of pH of 7.0 producing a filler-fiber composite with a surface area of 6-11 m2/g (˜60 to 80% PCC but can have more or less in composite)

TABLE 1


Breaking Length Physical Properties in Meters

Filler Loading	Scalenohedral	Aragonitic	Rhombohedral	Control
Levels	Filler-fiber	Filler-fiber	Filler-fiber	Filler-fiber

20	4,021	4,599	4,312	4,245
25	3,799	4,358	3,813	3,715
30	3,280	3,674	3,871	2,998

TABLE 2


Tensile Strength Physical Properties in kN/m

Filler Loading	Scalenohedral	Aragonitic	Rhombohedral	Control
Levels	Filler-fiber	Filler-fiber	Filler-fiber	Filler-fiber

20	3.062	3.555	3.397	3.382
25	3.124	3.324	2.999	3.021
30	2.658	2.785	3.005	2.448

TABLE 3


Internal Bond Strength Physical Properties in ft-lb

Filler Loading	Scalenohedral	Aragonitic	Rhombohedral	Control
Levels	Filler-fiber	Filler-fiber	Filler-fiber	Filler-fiber

20	237.70	264.07	283.13	255.67
25	263.20	285.95	251.65	256.95
30	242.63	248.60	273.65	249.53

The morphology controlled filler-fiber composite showed equivalent or greater physical properties (i.e. tensil strength, breaking length, and internal bond strength) as compared with the control filler-fiber.

TABLE 4


ISO Opacity Optical Properties

Filler Loading	Scalenohedral	Aragonitic	Rhombohedral	Control
Levels	Filler-fiber	Filler-fiber	Filler-fiber	Filler-fiber

20	89.20	88.20	87.38	88.18
25	89.93	89.15	88.78	89.55
30	90.95	90.40	89.68	90.83

TABLE 5


Pigment Scatter Optical Properties

Filler Loading	Scalenohedral	Aragonitic	Rhombohedral	Control
Levels	Filler-fiber	Filler-fiber	Filler-fiber	Filler-fiber

20	60.15	55.47	55.08	58.55
25	64.90	62.40	61.10	65.40
30	70.55	69.55	65.80	73.13

The morphology controlled filler-fiber composite showed equivalent optical properties (i.e. ISO Opacity and Pigment Scatter) as compared with the control filler-fiber. [0067]

Claims

We claim:

1. A filler-fiber composite comprising:

(a) feeding slake containing seed to a first stage reactor

(b) reacting the slake containing seed in the first stage reactor in the presence of carbon dioxide to produce a first partially converted calcium hydroxide calcium carbonate slurry

(c) reacting the first partially converted calcium hydroxide calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide and a heel to produce a second partially converted calcium hydroxide calcium carbonate slurry and

(d) reacting the second partially converted calcium hydroxide calcium carbonate slurry in a third stage reactor in the presence of carbon dioxide and fibers to produce a filler-fiber composite.

2. The filler-fiber composite of claim 1 wherein the fiber is from about 0.1 microns to about 2 microns in thickness and from about 10 microns to about 400 microns in length.

3. The filler-fiber composite of claim 2 wherein the filler is aragonite and has a specific surface area of from about 5 meters squared per gram to about 11 meters squared per gram.

5. The filler-fiber composite of claim 4 wherein the first partially converted calcium hydroxide calcium carbonate slurry is converted from about 41 percent to about 99 percent.

6. The filler-fiber composite of claim 5 wherein the second partially converted calcium hydroxide calcium carbonate slurry is converted to a filler-fiber composite.

7. A method for producing a filler-fiber composite comprising:

(a) feeding slake containing citric acid to a first stage reactor

(e) reacting the slake containing citric acid in the first stage reactor in the presence of carbon dioxide to produce a CaCO₃heel and

(f) adding slake containing sodium carbonate to the heel material of the first stage reactor in the presence of CO₂to produce a partially converted calcium hydroxide calcium carbonate slurry and

(g) reacting the partially converted calcium hydroxide calcium carbonate slurry in a second stage reactor in the presence of carbon dioxide and fibrils to produce a filler-fiber composite.

8. The method for producing the filler-fiber composite of claim 7 wherein the fiber is from about 0.1 microns to about 2 microns in thickness and from about 10 microns to about 400 microns in length.

9. The method for producing the filler-fiber composite of claim 8 wherein the filler is rhombohedral and has a specific surface area of from about 5 meters squared per gram to about 11 meters squared per gram.

10. The method for producing the filler-fiber composite of claim 9 wherein the calcium hydroxide calcium carbonate slurry is converted from about 20 percent to about 40 percent.

11. The method for producing the filler-fiber composite of claim 10 wherein the first partially converted calcium hydroxide calcium carbonate slurry is converted from about 41 percent to about 99 percent.

12. The method for producing the filler-fiber composite of claim 11 wherein the second partially converted calcium hydroxide calcium carbonate slurry is converted to a filler-fiber composite.

13. The filler-fiber composite of claim 1 utilized in paper or paperboard.

14. The filler-fiber composite of claim 7 utilized in paper or paperboard.

15. The paper produced utilizing the filler-fiber of claim 1.

16. The paper produced utilizing the filler-fiber of claim 7.