This application is the national phase under 35 U.S.C. § 371 of PCT International Application No. PCT/FR02/00574 which has an International filing date of Feb. 14, 2002, which designated the United States of America.
The present invention concerns a process for the manufacture of a sheet of paper containing calcium carbonate in the form of calcite.
Various types of paper are known to contain mineral fillers, in order, on one hand, to reduce their costs, since the fillers are less expensive than cellulose fibers, and, on the other hand, to provide or improve certain physical and mechanical characteristics. Materials specifically used as fillers are kaolin, talc, titanium oxide, aluminum hydroxide, satin white, and calcium carbonate in ground or precipitated form. The classic method for these fillers involves preparation ex situ at the time of manufacture of the paper; they are incorporated into the paper fibers and retained through the addition of retention agents.
The development of paper manufacturing in an alkaline environment, in order to make the paper more durable, has led to wider use of calcium carbonate.
Calcium carbonate presents a number of crystallographic forms. The most stable and most commonly-used form is calcite; another, somewhat less frequently used form is aragonite; the least stable form is vaterite. Calcite and aragonite crystals are rhombohedral in shape, whereas vaterite crystals are spherical.
Paper-making processes have been proposed which enable the calcium carbonate to be precipitated in situ onto paper fibers and fixed without the addition of retention agents.
Such processes have been described in the patents listed below.
Patent application WO 9942657 describes a new process for the synthesis of calcium carbonate in the presence of cellulose fibers, so as to obtain, at the end of the process, a calcium carbonate precipitate in situ on the fibers. This process is characterized by the inclusion of:
When all of these three ingredients are present, the calcium carbonate crystals are fixed onto the fibers, and a higher level of retention is obtained than when calcium carbonate is added to a paper composition that requires retention agents. This process is implemented in the dilute medium typically used in the paper-making process.
U.S. Pat. No. 5,679,220 also describes a method of fixing precipitated calcium carbonate onto paper fibers in a paper-making process using cellulose fibers, calcium hydroxide and carbon dioxide under high shearing as a precipitating gas. The patent envisages a variation in the molar ratio of the carbon dioxide to the calcium hydroxide in order to obtain calcium carbonate crystals of different morphologies. Nonetheless, this patent does not clearly show how to obtain the desired crystallographic form of calcium carbonate.
The objective of the present invention is to provide a sheet of paper that contains calcium carbonate in its common form of calcite and that has improved “look-through.”
The applicant has shown that it is possible to act on crystallographic forms of calcium carbonate through the use of the in situ precipitation process of calcium carbonate, by adjusting the order and the durations of contact between the various compositions involved, in order to precipitate and fix the calcium carbonate onto the fibers in situ when a sheet of paper is being manufactured. He has shown that the calcium carbonate precipitated according to in situ processes initially crystallizes in the form of vaterite, which is unstable before being transformed into its more stable form of calcite, and that this passage from vaterite to calcite could be controlled and used at the time of manufacture of the sheet of paper, in order to improve the fixation and distribution of the calcium carbonate crystals, in calcite form, within the paper.
The invention provides a process for the manufacture of a sheet of paper containing paper fibers and calcium carbonate, mostly in the form of calcite crystals directly linked to the paper fibers, wherein said process includes the following stages:
Preferably, the paper-manufacturing process is characterized by the fact that the composition containing calcium hydroxide is added after the composition containing calcium hydrogen carbonates and/or hydrated and/or dissolved carbon dioxide.
Preferably, the paper-manufacturing process is characterized by the fact that the composition containing calcium hydrogen carbonates results from a mixture, in an aqueous medium, of recycled calcium carbonate and carbon dioxide.
Preferably, the recycled calcium carbonate comes from recycled paper products, specifically recycled paper fibers and/or recycled white water.
Recycled white water originates in the water drained from the fibrous suspension on the wire of the paper-making machine. It contains fine elements, specifically fillers, such as calcium carbonate, and possibly other alkaline or alkaline-earth compounds and cellulose fibers (called “fine” fibers) which are not retained on the wire, these fibers themselves containing fillers. Like other possible sources of recycled paper products, there are recycled paper fibers which originate in old papers, specifically de-inked and possibly bleached papers, and recycled “casse paper”; these products also contain fillers, such as calcium carbonate and possibly other alkaline or alkaline-earth compounds. Another source might be de-inking sludge and other types of sludge from the paper-making process.
According to a particular embodiment of the invention, the carbon dioxide is added in different places in the cycle of the paper-making machine. Preferably, this addition is performed before the addition of the calcium hydroxide, in order to ensure the dissolution of the gas and thus to subsequently encourage the speed of the reaction with the calcium hydroxide in order to form the precipitated vaterite crystals.
Preferably, most of the carbon dioxide is added in the course of the white water recycling cycle of the paper-making machine. At the start of the cycle, the carbonic (carbon dioxide) gas participates in the solubilization of the recycled calcium carbonate, in the form of calcium hydrogen carbonates, present in the white water. The calcium carbonate will subsequently be recrystallized during reaction with the calcium hydroxide.
According to a particular embodiment of the invention, the process is characterized by the fact that the addition of said gaseous carbon dioxide takes place between the white water receiving site under the wire of the paper-making machine and the mineralizer. This will encourage full dissolution of the gas before the reaction with calcium hydroxide. In fact, it is preferable for the carbon dioxide to be added during the recycling cycle of the white water, so that it is entirely dissolved, in free form, in hydrated form, or in the form of calcium hydrogen carbonates or other alkaline or alkaline-earth salts, depending upon which of these ions are present.
An advantage of this process is that the fibers are not placed in contact with an alkaline product; this improves the homogeneity of the paper, which is known as “look-through,” because the fibers have a tendency to clump together in an alkaline environment. During recrystallization of the carbonate in the presence of fibers, the medium remains neutral; this improves the efficacy of the sizing agents and the optical agents, which are alkaline pH-sensitive.
An advantage of this process, introducing the carbonic gas at the beginning of the cycle (optimal dilution point for hydration of the gas) and in a machine adapted for mineralization of water, is that it is easier to use a gas with a low CO2 content, recovered from a boiler or a lime kiln, in order to transform it into calcium hydrogen carbonate.
According to a particular embodiment of the invention, the process is characterized by the fact that the carbon dioxide is introduced in the form of diluted carbonic gas, specifically fumes from a boiler or a limekiln, containing 8% to 25% of CO2.
In the process according to the invention, the molar ratio of carbon dioxide to calcium hydroxide is equal to approximately 1, and is therefore stoichiometric.
Furthermore, the process according to the invention is also advantageously characterized by the fact that the dilution rate of the paper fibers in the final reaction mixture ranges from 0.1% to 5% by weight, preferably from 0.2% to 1.5%.
Preferably, the process according to the invention is characterized by the fact that the composition containing the calcium hydroxide is an aqueous suspension of solid particles of said calcium hydroxide, known as milk of lime.
More particularly, the process according to the invention is characterized by the fact that the calcium hydroxide is in the form of an aqueous suspension of solid particles with a grading lower than 10 μm, preferably between 0.5 and 2 μm, and particularly on the order of 1 μm.
Let us assume that an industrial installation manufactures 5.4 metric tons of paper per hour, characterized by the following operating conditions for the principal cycles:
The gas reacts almost instantaneously with the milk of lime, in order to form, in suspension in the water, unstable vaterite crystals between points a and b; subsequently, after being mixed with the fibrous suspension (2, 2′) and before reaching the headbox (E), the vaterite crystals are transformed into stable calcite. The suspension of fibers and fillers is then conveyed onto the wire of the paper-making machine (M) for drainage and formation of the sheet of paper.
When the virgin fibers and the recycled paper are added, the pH of the suspension is stabilized at its final value, adjustable between 7 and 8 as desired, which corresponds to a calcium-carbon balance of the water.
The output of the paper-making machine consists of 5.4 tons of paper with a 26% filler of crystals, essentially in the form of rhombohedral calcite.
The size of the calcite crystals becomes smaller as the grading of the milk of lime becomes finer. The paper obtained will accordingly be more opaque when the milk of lime used contains grains less than 1 μm in dimension.
The high opacity of the sheet (6) is obtained by virtue of the very consistent distribution of the crystals hooked on to the fibers, without the help of a retention agent and without any variation in the pH. In comparison with the traditional process of filler retention with formation of aggregates by means of a retention agent, the improvement in opacity is between 3 and 4 points.
A sheet of paper is made according to the prior art whereby calcium carbonate is precipitated in situ, mixing the compounds at the same time without specifically adding the paper fibers last, and without adding them immediately after implementing the precipitation of the calcium carbonate.
It will be noted that the sheet of paper obtained according to the invention contains calcite crystals that are better distributed than those in the sheet of paper prepared according to the prior art, and that, accordingly, the “look-through” of said sheet of paper obtained according to the invention is improved.
Number | Date | Country | Kind |
---|---|---|---|
01 02186 | Feb 2001 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/FR02/00574 | 2/14/2002 | WO | 00 | 1/20/2004 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO02/066735 | 8/29/2002 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3321269 | Eizo Yasui et al. | May 1967 | A |
3458329 | Hatch et al. | Jul 1969 | A |
3578603 | Dale et al. | May 1971 | A |
4124688 | Shibazaki et al. | Nov 1978 | A |
4781818 | Reagan et al. | Nov 1988 | A |
4818373 | Bartholic et al. | Apr 1989 | A |
5232678 | Bleakley et al. | Aug 1993 | A |
5262006 | Andersson et al. | Nov 1993 | A |
5494651 | Minayoshi et al. | Feb 1996 | A |
5679220 | Matthew et al. | Oct 1997 | A |
5695733 | Kroc et al. | Dec 1997 | A |
5792440 | Huege | Aug 1998 | A |
5851655 | Tokiyoshi et al. | Dec 1998 | A |
6251222 | Silenius et al. | Jun 2001 | B1 |
6251356 | Mathur | Jun 2001 | B1 |
6310129 | Lilly et al. | Oct 2001 | B1 |
6387212 | Christian | May 2002 | B1 |
6706148 | Joisson et al. | Mar 2004 | B1 |
20030094252 | Sundar et al. | May 2003 | A1 |
Number | Date | Country |
---|---|---|
WO 9942657 | Aug 1999 | WO |
Number | Date | Country | |
---|---|---|---|
20040118542 A1 | Jun 2004 | US |