EP2443280A1 - Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill - Google Patents
Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper millInfo
- Publication number
- EP2443280A1 EP2443280A1 EP10789951A EP10789951A EP2443280A1 EP 2443280 A1 EP2443280 A1 EP 2443280A1 EP 10789951 A EP10789951 A EP 10789951A EP 10789951 A EP10789951 A EP 10789951A EP 2443280 A1 EP2443280 A1 EP 2443280A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- rejects
- alkaline
- fiber
- alkali
- hydrogen peroxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/001—Modification of pulp properties
- D21C9/002—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
- D21C9/005—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives organic compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/001—Modification of pulp properties
- D21C9/007—Modification of pulp properties by mechanical or physical means
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/16—Bleaching ; Apparatus therefor with per compounds
- D21C9/163—Bleaching ; Apparatus therefor with per compounds with peroxides
Definitions
- the present invention is directed to processes producing mechanical pulps utilizing refiners for improving the quality of screen rejects, and most particularly to a mechanical pulp mill integrated with a neutral-alkaline papermaking process producing mechanical printing paper grades.
- the rejects are treated with hydrogen peroxide, an alkali and an organic stabilizing agent to provide improved optical and physical properties of the refined rejects.
- Mechanical pulping is a process of mechanically triturating wood into its fibers for the purpose of making pulp.
- a key advantage of mechanical pulping is the high yield compared to chemical pulping which removes most or all of the lignin binding the cellulose fibers. Lignin is not removed from mechanically pulped wood, meaning scarce resources are more efficiently utilized.
- Pulps made using conventional mechanical pulping methods are mainly used for newsprint and other printing papers destined for direct mail advertising, directories and some magazines and books, and are typically unsuitable for higher quality or more durable paper end products. This is due, in part, to the fact that mechanical pulps are generally more difficult to bleach, can revert in terms of brightness due to light and humidity exposure and typically have lower strength than chemical pulps.
- the TMP process typically consists of two refining stages.
- the first stage is pressurized, which allows the capture of thermal energy released as steam when mechanical energy is applied to the wood chips between the rotating refiner discs. Control of the steam pressure allows the primary refiner to operate at elevated temperatures and provides steam to heat and moisturize the wood chips before refining.
- the second stage refiner may be atmospheric, but it is more common to pressurize that stage also in order to capture more energy and better control the process. Pulps made by the TMP and CTMP processes have higher strength, which makes them the more favored mechanical pulping processes. However, there is still potential for improvement.
- the TMP process consumes a high quantity of electrical energy and the pulp produced by the TMP process tends to be darker than most other pulps due to thermal darkening of fiber during refining. Furthermore, the presence of large quantities of lignin in the refined fiber makes it highly susceptible to alkaline darkening.
- alkaline peroxide treatment of mechanical pulp rejects has been shown to produce improved physical properties and higher brightness equal to or superior to those of sulphonation.
- efficient alkaline peroxide treatments have been described as requiring a treatment time of from five to forty minutes or more to provide maximum improvements. See for example " HIGH ALKALINE PEROXIDE TREATMENT OF WHITE SPRUCE/LODGEPOLE PINE RMP REJECTS', S.G. Book, ppl-17, CPPA Pacific Coast Brach Mini- Conference April 1990 and "ALKALINE PEROXIDE TREATMENT OF SOUTHERN PINE TMP REJECTS", MJ. Sferrazza et al., pp 617- 629, 1988 Pulping Conference. In the described processes, 4.4-8.9% by weight NaOH based on fiber was being utilized to treat rejects in order to achieve the physical strength improvements noted and caustic/ peroxide (C/P) ratios of 2-3 : 1 were utilized.
- C/P caustic/ peroxide
- US Patent Publication No. 2009/0032207 discloses a mechanical or chem. -mechanical process for making pulp in which, after fibrillation, the pulp is bleached in alkaline conditions. Thereafter, the rejects are screened and bleached separately from the accepts and the bleached rejects mixed with the accepts.
- US Patent Publication 2008/0035286 discloses an alkaline peroxide mechanical pulping process which includes a step of treating fiberized lignocellulosic material with alkali peroxide chemical for a time and under conditions sufficient to obtain a pulp of desired consistency.
- Bleaching is a term associated with a pulping process whereby certain chemicals are well mixed with fiber and then retained on the fiber for a given amount of time to increase the pulp's brightness. Bleaching is practiced on chemical and mechanical fiber pulps. In mechanical pulping, the increase in brightness is achieved by altering the chemical structure of the conjugated double bonds in lignin. The conjugated double-bonded species are called chromophores. "Brightening” is the term often used when referring to bleaching of mechanical pulps to distinguish it from the bleaching process of chemical pulps, which differs by the removal all lignin. As used hereinafter “bleaching" will be intended to cover the process of "brightening" as well.
- Brightening is often carried out in a single step in the pulping process.
- the bleaching process is conventionally carried out in a bleaching train in one or a plurality of vessels (bleach towers or stages) in a distinct section of the mill, as opposed to the pulping section of the mill.
- Brightening can be carried out using oxidizing agents such as hydrogen peroxide and/or reducing agents such as sodium dithionite or sodium hydrosulfite.
- hydrogen peroxide an oxidizing agent
- sodium hydroxide is a strong alkali and provides the requisite high pH necessary to produce the active perhydroxyl ion, HOO " , thought to produce the bleaching effect in pulps.
- the cost of sodium hydroxide has been increasing due to changes in availability and energy costs. Concern over the environment has also meant a decrease in the available sodium hydroxide supply. Therefore, different alkali sources and different methods have been tried to find suitable alternatives for bleaching liquors and bleaching processes with limited commercial success.
- sodium silicate and one of various organic and inorganic stabilizing agents are typically applied to fiber during and prior to addition of hydrogen peroxide and alkali on the fiber.
- These materials are beneficial largely due to their ability to control metal ions such as manganese, iron and copper that are contained in wood chips entering the pulping process. If untreated, these metal ions destroy hydrogen peroxide and perhydroxyl ion before it is able to brighten chromophores, making the process must less cost efficient and lowering brightening performance.
- the present invention specifically excludes the use of sodium silicate for stabilization of peroxide and perhydroxyl ion.
- the presence of silicates can result in the formation of scales (eg. calcium silicate, sodium carbonate) such as on refiner plates which can limit the ability of the refiner to refine rejects.
- scales eg. calcium silicate, sodium carbonate
- Figure 1 is a bar graph of ISO Brightness of Refined Screen Rejects based upon Example 1.
- Figure 2 is a graph of ISO Brightness of Refined Screen Rejects versus % Peroxide based upon Example 1.
- Figure 3 is graph of Bulk of Refined Screen Rejects versus Caustic based upon Example 1.
- Figure 4 is a graph of ISO Brightness versus Applied Peroxide in bleaching TMP Screened Stock based upon Example 1.
- Figure 5 is a graph of the % bulk decrease and % tensile strength increase compared to baseline from APTR at increasing C/P of Rejects Screen Accepts based upon Example 2.
- Figure 6 is a graph of the %Long Fiber due to APTR at increasing C/P of Rejects Screen Accepts and TMP Screened Stock based upon Example 2.
- Figure 7 is a graph of the %bulk decrease and % strength increase compared to baseline from APTR at increasing C/P of TMP Screened Stock based upon Example
- Figure 8 is a graph of brightness measured on stock at various points through the TMP mill before, during and after a 7-day APTR trial at a 1.0 C/P based upon Example 2.
- Figure 9 is a graph of total specific energy in rejects refining versus final rejects freeness with compared to without APTR after a 7-day APTR trial at a 1.0 C/P based upon Example 2.
- Figure 10 is a graph of wet-end breaks by day for all downstream paper machines before, during and after a 7-day APTR trial at a 1.0 C/P based upon Example 2.
- Figure 11 is a graph of key pulp properties from pulp sampled at the Rejects Refiner Discharge after applying a moderate hydrogen peroxide dosage based upon Example 3.
- Figure 12 is a graph of key pulp properties from pulp sampled at the Rejects Refiner Discharge after applying a higher hydrogen peroxide dosage based upon Example 3.
- the present invention is directed to an improved process for the treatment of mechanical pulping rejects fiber wherein an alkaline hydrogen peroxide treatment is employed that does not require retention time on fiber prior to high consistency refining and which is effective at low chemical treatment levels.
- the use of zero retention time when adding alkaline treatment chemicals to thickened rejects prior to refining was found to be effective at caustic addition rates of less than or equal to 3.5% by weight in paper mills which operate at least one integrated neutral-alkaline papermaking machine and recycle water from this back to the mechanical pulp mill.
- percentages are by weight unless specifically specified otherwise. Elimination of the requirement for retention of alkaline peroxide on rejects fiber prior to refining allows the present invention to be implimented with minimal capital cost.
- Recycle of neutral-alkaline paper machine white water to the mechanical pulp mill and the buffering associated with it from precipitated calcium carbonate (PCC) or ground calcium carbonate (GCC) filler pigment minimizes operating chemical costs by reducing the alkali demand of the mechanical fiber. This results in lower addition of total alkali on the rejects.
- the amount of hydrogen peroxide added when alkaline treating rejects is related to caustic additon so lower caustic requirements result in lower hydrogen peroxide requirements and makes the process more cost-effective.
- C/P caustic to peroxide ratio
- ATR alkaline peroxide treatment of rejects
- alkali is meant to include any source of alkalinity such as sodium hydroxide or caustic soda (NaOH), sodium carbonate (Na 2 CO 3 ) and sodium bicarbonate (NaHCO 3 ).
- Na 2 CO 3 and NaHCO 3 also provide buffer capacity to prevent wide swings in pH. When alkaline peroxide bleaching at high temperatures, better brightness is obtained with buffered systems. Buffering the system at lower pH (preferably between about 9 to about 10.5) prevents peroxide decomposition and darkening, but still provides adequate alkalinity to produce the desired species. The buffer releases alkalinity as necessary, and provides sufficient alkalinity for a slow and even production of the perhydroxyl ions.
- the calcium carbonate functions as a buffer and would be expected to improve brightening during APTR that occurs in a high temperature refiner.
- the components of the APTR liquor may be added separately or concurrently, concurrently meaning two or more components together such as a pre-mixed stream and separately meaning one at a time, as in individual streams.
- a hydrogen peroxide stabilizer such as a suitable chelating agent may be included.
- Chelating agents can include, but are not limited to aminopolycarboxylic acids, (e.g.) ethylenediaminetetraacetic acid (EDTA), diethylene triamine pentaacetic acid (DTPA), nitrilotriacetic acid (NTA), phosphonic acids, (e.g.) ethylenediaminetetramethylene-phosphonic acid (EDTMP), diethylenetriaminepentamethylenephosphonic acid (DTPMP), nitrilotrimethylenephosphonic acid (NTMP), polycarboxylic acids, gluconates, citrates, polyacrylates, and polyaspartates or any combination thereof.
- aminopolycarboxylic acids e.g.) ethylenediaminetetraacetic acid (EDTA), diethylene triamine pentaacetic acid (DTPA), nitrilotriacetic acid (NTA), phosphonic acids, (e.g.)
- a chelating agent may be added to the bleaching liquor in an amount up to 0.5% by weight based on fiber but is preferably added at addition rates of from about 0.1-0.25% based on fiber.
- chelating agents may be added separately or concurrently with one or more bleach liquor components at one or more chemical addition points in the refining system. Chelating agents are thought to bind metals to prevent the decomposition of hydrogen peroxide which can cause darkening of the produced paper.
- neutral-alkaline it is meant a pH of about 7.0 to 7.5. Additionally, it was found that neutral-alkaline Whitewater containing significant amounts of non-oxidized sulfur compounds leads to brightness gains during APTR that are lower than those where the neutral-alkaline Whitewater does not contain these impurities.
- Figures 1-4 summarize the relationships observed after APTR on fiber from laboratory-prepared handsheets made from Refined Screen Rejects and brightened TMP Screened Stock samples.
- Trials were conducted at an integrated neutral-alkaline mechanical printing paper mill producing a range of paper grades having brightness specifications of 58-84% ISO and printing opacity specification of 85-97%. During extended operating periods of 12 hours and separately, 7 days, APTR was evaluated by applying a liquor containing dilution water, DTPA, caustic soda and hydrogen peroxide onto feedstock for two rejects refiners operating in parallel.
- the 12-hour evaluations allowed: a) comparing results from two different addition points around the refiners, b) evaluating a low (0.6) and a medium (1.0) C/P ratio at a constant hydrogen peroxide addition of 30 kg/BDt to determine effects on fiber quality at various locations in the TMP mill that the rejects refiners were operating in and c) determining how rejects refining specific energy was impacted by APTR.
- the 7 day and 24 hour per day evaluation were at a 1.0 C/P with addition of 30 kg/BDt peroxide on rejects and a) allowed paper machine Whitewater coming back to the TMP mill to completely turn over, b) evaluated downstream effects of APTR in bleaching of TMP on the paper machines on various paper grades and c) provided data showing specific energy reduction in rejects refining.
- Table 2 summarizes laboratory data of accepts samples collected during a single week of primary, secondary and rejects screens when two APTR operating periods of 12 hours each in duration could be compared to three operating periods surrounding them when APTR was not operating.
- Figures 5-7 illustrates the key benefits of APTR in the TMP mill during the 12 hour trials while Figures 8-10 summarize key results of continuous automated testing in the TMP mill and at the three downstream paper machines over the extended 7 day trial.
- Trials were conducted at an integrated neutral-alkaline mechanical printing paper mill producing a limited number of paper grades having brightness specifications of 58- 60% ISO and printing opacity specification of 85-95%.
- APTR was evaluated by applying a liquor containing dilution water, DTPA, caustic soda and hydrogen peroxide into high-pressure dilution feed water added at the refining zone of one or two atmospheric refiners operating in series. These refiners process screened, cleaned TMP rejects that are subsequently bleached separately from additional TMP accepts/rejects with sodium hydrosulfite and utilized as a reinforcing fiber on two downstream paper machines.
- Figures H and 12 illustrate the beneficial effects of APTR on brightness, tensile and other key pulp properties utilizing Cf? ratios in the range of 0.35-0.40 in treatment liquor and DTPA applied into Unrefined Rejects prior to refining.
Landscapes
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Paper (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18707309P | 2009-06-15 | 2009-06-15 | |
| PCT/US2010/037880 WO2010147812A1 (en) | 2009-06-15 | 2010-06-09 | Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP2443280A1 true EP2443280A1 (en) | 2012-04-25 |
| EP2443280A4 EP2443280A4 (en) | 2014-08-13 |
| EP2443280B1 EP2443280B1 (en) | 2020-12-09 |
Family
ID=43356689
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10789951.0A Not-in-force EP2443280B1 (en) | 2009-06-15 | 2010-06-09 | Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20120097350A1 (en) |
| EP (1) | EP2443280B1 (en) |
| CN (1) | CN102459753A (en) |
| RU (1) | RU2495177C2 (en) |
| WO (1) | WO2010147812A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102776795B (en) * | 2012-08-03 | 2014-06-04 | 常州市春江化学有限公司 | Application of organic phosphonic acid in pulp bleaching process |
| CA2824076A1 (en) | 2012-08-21 | 2014-02-21 | University Of New Brunswick | System and method for reclaiming rejects in sulfite pulping |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE441282B (en) * | 1984-02-22 | 1985-09-23 | Mo Och Domsjoe Ab | PROCEDURE FOR THE PREPARATION OF IMPROVED HOG REPLACEMENT MASS |
| US4614646A (en) * | 1984-12-24 | 1986-09-30 | The Dow Chemical Company | Stabilization of peroxide systems in the presence of alkaline earth metal ions |
| AUPM452794A0 (en) * | 1994-03-17 | 1994-04-14 | Amcor Limited | Waste water recovery system |
| AU4271596A (en) * | 1995-12-19 | 1997-07-14 | Kvaerner Hymac Inc. | Process for treating refiner pulp |
| DE69912128T2 (en) * | 1998-04-17 | 2004-06-17 | Alberta Research Council, Inc., Edmonton | METHOD FOR PRODUCING LIGNOCELLULOSE-CONTAINING PULP FROM NON-WOODY MATERIAL |
| CA2356444C (en) * | 1999-02-15 | 2009-12-15 | Kiram Ab | Process for oxygen pulping of lignocellulosic material and recovery of pulping chemicals |
| US6881299B2 (en) * | 2001-05-16 | 2005-04-19 | North American Paper Corporation | Refiner bleaching with magnesium oxide and hydrogen peroxide |
| US6743332B2 (en) * | 2001-05-16 | 2004-06-01 | Weyerhaeuser Company | High temperature peroxide bleaching of mechanical pulps |
| GB0413068D0 (en) | 2004-06-11 | 2004-07-14 | Imerys Minerals Ltd | Treatment of pulp |
| FI121311B (en) | 2005-05-03 | 2010-09-30 | M Real Oyj | A process for the preparation of a mechanical pulp for use in the manufacture of paper and board |
| RU2322504C1 (en) * | 2006-06-26 | 2008-04-20 | Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова Российской академии наук | Method for preparing genetic-engineering human insulin |
| US8262851B2 (en) | 2006-08-10 | 2012-09-11 | Andritz Inc. | Processes and systems for the pulping of lignocellulosic materials |
| US8865101B2 (en) * | 2006-08-25 | 2014-10-21 | Robert A. Rossi | Process and system for producing commercial quality carbon dioxide from high solids lime mud |
-
2010
- 2010-06-09 US US13/264,206 patent/US20120097350A1/en not_active Abandoned
- 2010-06-09 WO PCT/US2010/037880 patent/WO2010147812A1/en not_active Ceased
- 2010-06-09 CN CN2010800264508A patent/CN102459753A/en active Pending
- 2010-06-09 EP EP10789951.0A patent/EP2443280B1/en not_active Not-in-force
- 2010-06-09 RU RU2011142599/12A patent/RU2495177C2/en active
Also Published As
| Publication number | Publication date |
|---|---|
| RU2495177C2 (en) | 2013-10-10 |
| EP2443280B1 (en) | 2020-12-09 |
| WO2010147812A1 (en) | 2010-12-23 |
| RU2011142599A (en) | 2013-04-27 |
| EP2443280A4 (en) | 2014-08-13 |
| US20120097350A1 (en) | 2012-04-26 |
| CN102459753A (en) | 2012-05-16 |
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