US20150267349A1 - Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production - Google Patents

Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production Download PDF

Info

Publication number
US20150267349A1
US20150267349A1 US14/733,067 US201514733067A US2015267349A1 US 20150267349 A1 US20150267349 A1 US 20150267349A1 US 201514733067 A US201514733067 A US 201514733067A US 2015267349 A1 US2015267349 A1 US 2015267349A1
Authority
US
United States
Prior art keywords
pulp
enzyme
pitch
oven
esterase
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.)
Abandoned
Application number
US14/733,067
Inventor
Xiang H. Wang
Jian Hua Ma
Chengliang Jiang
Howard Kaplan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Enzymatic Deinking Technologies LLC
Original Assignee
Enzymatic Deinking Technologies LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Enzymatic Deinking Technologies LLC filed Critical Enzymatic Deinking Technologies LLC
Priority to US14/733,067 priority Critical patent/US20150267349A1/en
Assigned to ENZYMATIC DEINKING TECHNOLOGIES, L.L.C. reassignment ENZYMATIC DEINKING TECHNOLOGIES, L.L.C. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JIANG, CHENGLIANG, KAPLAN, HOWARD, MA, JIAN HUA, WANG, XIANG H.
Publication of US20150267349A1 publication Critical patent/US20150267349A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/02Agents for preventing deposition on the paper mill equipment, e.g. pitch or slime control
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-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
    • D21C9/08Removal of fats, resins, pitch or waxes; Chemical or physical purification, i.e. refining, of crude cellulose by removing non-cellulosic contaminants, optionally combined with bleaching
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-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
    • D21C9/08Removal of fats, resins, pitch or waxes; Chemical or physical purification, i.e. refining, of crude cellulose by removing non-cellulosic contaminants, optionally combined with bleaching
    • D21C9/086Removal of fats, resins, pitch or waxes; Chemical or physical purification, i.e. refining, of crude cellulose by removing non-cellulosic contaminants, optionally combined with bleaching with organic compounds or compositions comprising organic compounds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H11/00Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D21H11/08Mechanical or thermomechanical pulp
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/005Microorganisms or enzymes
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • D21H17/56Polyamines; Polyimines; Polyester-imides
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/66Salts, e.g. alums

Definitions

  • the present invention is generally in the field of managing wood pitch using enzyme treatment of wood pulp.
  • Wood resin is composed of fatty acids and resin acids, triglycerides, steryl esters, and sterols. Wood resins, as well as other extractives such as lignins, pectins, and phenols, are the major components of pitch deposits.
  • the encapsulated resin is liberated from ray parenchyma cells and resin canals. Some of the dispersed resin droplets precipitate onto fiber surfaces, impairing fiber to fiber bonding and thereby negatively affecting the physical properties of the pulp. Dispersed resin which precipitates later in the pulping and papermaking processes can affect paper machine runnability and reduce paper quality, resulting in increased manufacturing costs.
  • pitch deposits in pulping and paper manufacturing processes have been reduced by seasoning wood logs and chips, and by the use of physiochemical control agents.
  • cationic coagulant chemicals have been used to fix the extractives to the fibers so that the pitch particles can be removed with the paper products and therefore reduce and/or eliminate the pitch related deposit on the manufacturing equipment.
  • Traditional methods include alum, talc, bentonite, surfactants, pitch stabilizer, detackifiers, and polymers.
  • those traditional methods have their limitations due to the complexities of pulping and paper making process, particularly when used with recycled paper.
  • Laccase has been used in some cases to treat pulp, see for example, U.S. Pat. Nos. 5,691,193; 6,242,245; U.S. Pat. No. 6,610,172; and International Publication No. WO 92/09741.
  • Other methods have used enzymes such as lipase and cellulase.
  • U.S. Pat. No. 7,125,471 discloses the use of enzyme compositions containing at least one esterase and at least one lipase for treating sludge added to pulp.
  • U.S. Pat. No. 6,939,437 discloses the use of cationic colloidal alumina microparticles, at least one polymer and optionally a cellulolytic enzyme for the treatment of pulp.
  • 2007/0261806 and 2006/0048908 disclose enzyme formulations for treating pulp (see also U.S. Pat. Nos. 6,770,170; 6,712,933 for additional treatments including enzymes).
  • the treatment pH may be in the range of 3.5 to 12 and the temperature range may be in a range between 35° C. and 90° C.
  • U.S. Pat. No. 5,616,215 discloses the use of lipase and aluminum salt to treat pulp containing mechanical pitch (triglycerides), wherein the treatment pH was in the range of 4-5.5 and the temperature was in the range of 30-70° C.
  • thermomechanical pulping (TMP) mills usually are run at temperatures ranging from 70 to 98° C. This temperature range is too high for even what is today known as thermophilic enzymes.
  • TMP thermomechanical pulping
  • the application of normal lipolytic enzymes disclosed in the prior art is limited or even impossible at such high temperatures.
  • the application of “normal” enzymes would require cooling of pulp stocks by addition of cold water, prior to enzyme treatment. The additional cooling creates many problems, for example, temperature shock to the system, increased fresh water usage, and increased demand of a mill's wastewater treatment capacity. The addition of cooling water can cause energy loss in a mill.
  • pitch containing pulp is treated with an effective amount of metal ions selected from the group consisting of aluminum, calcium, magnesium, iron, copper, zinc, titanium and zirconium prior to treatment with a lipolytic enzyme formulation.
  • pitch containing pulp is treated with an effective amount of a cationic polymer.
  • the pulp is treated with an effective amount of alum.
  • the pulp is treated with an effective amount of a metal ion or cationic polymer effective to increases stability of the enzyme at high temperature and at broad pH ranges of 3-11.
  • the method can be applied to any pitch-containing pulp, such as GW (Ground Wood), TMP (Thermo Mechanical Pulp), CTMP (Chemical Thermo Mechanical Pulp), Recycled ONP (old news paper), and/or their combinations.
  • GW Round Wood
  • TMP Thermo Mechanical Pulp
  • CTMP Complementary Thermo Mechanical Pulp
  • Recycled ONP old news paper
  • Examples are pulps produced by mechanical pulping, alone or combined with a certain chemical treatment.
  • the disclosed method enables treatment of pulp with normal a lipolytic enzyme to work at temperature range from about 70° C. to 98° C., preferably from about 70° C. to 90° C.
  • the wood pulp can be treated for a period of time from about 0.1 to 36 hours, more preferably from about 1.0 to about 12 hours.
  • the addition of metal ions or cationic polymers to the pulp prior to enzyme treatment stabilizes the enzyme formulation and speeds up the enzymatic reactions at high temperature and broader pH range. This enhances the effectiveness of the enzyme formulation in removing extractives such as long chain triglycerides whose conversion is favored thermodynamically at high temperatures. Additionally, the ability of the enzyme formulation to be active at high temperatures decreases the need for adding cooling water prior to enzyme treatment, thus reducing the fresh water use and costs associated with waste waster treatment.
  • the ability of the enzyme formulation to be active at lower pH (as low as 3.0) and higher pH (as high as 10.5) reduces the need for acid or base usage for pH adjustment of pulp stocks prior to enzyme treatment. It makes it possible for enzyme to be added to the locations where the conditions can be too harsh for normal lipolytic enzymes with the use of method described herein. In addition, the chemical costs can be reduced.
  • FIG. 5 is a graph showing the effect of metal ions on TG conversion using EnzOx® A under normal conditions at 65° C. and pH5.0-5.2.
  • FIG. 6 is a graph showing the relative enzyme activity (compared to the formulation freshly made with water dilution) of formulations (containing EnzOx® A) as a function of storage time under elevated temperature (40° C.), without and with addition of a cationic polymer (Polymer A).
  • Pitch refers to a composition composed of primarily triglycerides (TG), resin acids, fatty acids, waxes, resin esters, fatty alcohols, sterols, and terpenes, which are released from wood fibers during chemical and mechanical pulping processes. These resinous substances usually react with metal ions in the pulp stream and whitewater system which are added by the requirement of mill processes precipitate as aluminum, calcium, and magnesium salts, which may cause problems with the wet end components of paper machines.
  • TG triglycerides
  • Apparent pitch or “depositable pitch”, as used herein, refers to pitch which is located on the surface of the wood chips or sawdust or wood pulp is suspended in the aqueous phases as dissolved colloidal particles. Apparent pitch content is distinguished from total pitch content or total wood extractives, which includes pitch located on the surface of the wood chips or sawdust or wood pulp as well as pitch encapsulated or trapped within the wood fibers.
  • “Stone ground wood pulp”, as used herein, refers to pulp which is produced by grinding wood or wood chips into relatively short fibers with stone grounding. This pulp is used mainly in newsprint and wood-containing papers, such as lightweight coated (LWC) and super-calendared (SC) papers.
  • LWC lightweight coated
  • SC super-calendared
  • TMP Thermo Mechanical Pulp
  • pulp that is produced by a thermo-mechanical process where wood chips or sawdust are softened by steam before entering a pressurized refiner.
  • TMP generally has the same end-uses as stone groundwood pulp.
  • “Semi-chemical pulp”, as used herein, refers to pulp produced in a manner similar to TMP but the wood chips and/or sawdust are chemically treated before entering the refiner. This pulp has properties suited to tissue manufacture.
  • “Chemical pulp”, as used herein, refers to pulp produced by the treatment of wood chips or sawdust with chemicals to liberate the cellulose fibers by removing binding agents such as lignin resins and gums.
  • Sulphite and Sulphate pulping, or Kraft are two types of chemical pulping. Kraft is the predominant pulping process in chemical pulp production.
  • Recycled pulp or “recycled fibers” refers to fiber components of a paper or paperboard furnish that is derived from recycled paper and paperboard or wastepaper.
  • Suitable esterases include but are not limited to, are phospholipases (EC 3.1.1.32 and EC 3.1.1.4), carboxyl esterases (EC 3.1.1.1), pectinesterase (EC 3.1.1.11), lipolytic enzymes (EC 3.1.1.3) and acetyl esterase (EC 3.1.1.6) or acetyl esterase, which hydrolyze carboxylic esters.
  • phospholipases EC 3.1.1.32 and EC 3.1.1.4
  • carboxyl esterases EC 3.1.1.1
  • pectinesterase EC 3.1.1.11
  • lipolytic enzymes EC 3.1.1.3
  • acetyl esterase EC 3.1.1.6
  • acetyl esterase which hydrolyze carboxylic esters.
  • examples of other suitable lipolytic enzymes include cholesterol esterase (EC 3.1.1.13), which hydrolyses sterol esters.
  • Pectin esterase breaks the ester bond linking the pectin groups. Pectin is
  • Mono-, di- and triglycerides in a wood pulp sample can be reduced, i.e. hydrolyzed, in the presence of a lipolytic enzyme, such as a lipase, to form glycerol and fatty acids.
  • a lipolytic enzyme such as a lipase
  • the lipolytic enzyme is a non-selective lipase (EC 3.1.1.3) that can hydrolyze the ester bonds at all three locations in the glyceride structure.
  • Suitable lipases for the hydrolysis of triglycerides may be derived from plant, animal, or preferably microbial sources. Examples of sources for microbial lipases include Candida rugosa, Rhizopus arrhizus , and Chromobacterium viscosum .
  • Other suitable lipolytic enzymes belong to the family of carboxylic ester hydrolases. Representative examples of these include phospholipases, lipoprotein lipases, and acylglycerol lipases
  • EnzOx® A, B and C are three of the commercially formulated pitch control products from Enzymatic Deinking Technologies, LLC, Norcross, Ga. 30093.
  • the EnzOx® products contain principally esterases, cellulases, hemicellulase, amylases, and pectinases.
  • the enzyme formulation is EnzOx® A containing a normal temperature lipase, Resinase® A2X, Novozymes A/S.
  • the working temperature is from 45 to 70° C. with optimum temperature from 55 to 65° C.; the working pH range is from 4.0 to 7.5 with optimum pH range from 4.5 to 6.5.
  • the enzyme formulation is EnzOx® B, which comprises a commercial thermostable lipolytic enzyme, Resinase® HT, Novozymes A/S.
  • the working temperature range is from 55 to 85° C. with optimum from 65 to 80° C.
  • Metal ions that can be used to catalyze the enzymatic reaction of esterases and stabilize the enzyme formulations at high temperature, at alkaline pH, at neutral ph, and at acidic pH conditions include but are not limited to, aluminum, calcium, magnesium, iron, copper, zinc, titanium, and zirconium.
  • the aluminum ion can be provided by any aluminum salt that is soluble or partially soluble under the conditions of the mill processes.
  • the aluminum ion is provided by Papermaker's alum.
  • aluminum sulfate or aluminum chloride is used to provide the aluminum salt.
  • Calcium chloride, magnesium chloride, zinc sulfate, copper sulfate, iron sulfate or chloride, titanium chloride, and zirconium sulfate can also be used.
  • the pitch containing pulp is treated with the metal ions either prior to or together with addition of the enzyme formulation into pulps with sufficient mixing. It is preferred that metals ions are added to the pulp before the enzyme addition.
  • the metal ion or cationic polymer treatment enables EnzOx® A to be active over a temperature range from about 70 to 98° C., more preferably from about 75 to 85° C. instead of optimum range from 55 to 65° C. for the control; and at a pH range from 3.0 to 11, more preferably from about 7 to 10 instead of optimum pH range from 4.5 to 6.5 for the control.
  • the concentration of esterase enzymes used to treat pulp is from 0.005% to 1.0% based on oven dried fibers, preferably 0.005% to about 0.1% based on O.D.
  • the concentration of the metal ions or cationic polymers is from 1-100 lbs per ton based on oven dried fibers, preferably 10-60 lbs per ton based on O.D. fibers.
  • the addition of the metal ions to wood pulp enables the treatment of wood pulp at higher temperature and wider pH ranges.
  • Water soluble polymers such as a cationic water soluble polymer can be used to stabilize the enzyme formulation and increase the enzyme's catalytic activity, like the metal ions mentioned above.
  • examples of such polymers include epichlorohydrin/dimethylamine polymers (EPI-DMA) and cross-linked solutions thereof, polydiallyl dimethyl ammonium chloride (DADMAC), polyethylenimine (PEI), hydrophobically modified polyethylenimine, polyamines, resin amines, polyacrylamide, DADMAC/acrylamide copolymers, and ionene polymers.
  • Examples of ionene polymers include those set forth in U.S. Pat. Nos. 5,681,862, 5,575,993, and 5,256,252.
  • polymers can be used in any amount and preferably in dosage ranges from about 0.1-10 lbs per ton based on O.D. fibers, more preferably from 0.5 to 5 lbs/ton based on O.D. fibers.
  • the enzyme formulations are generally added to the pulp chests, preferably together with metal ions or cationic polymers at a place where sufficient mixing and retention time are available.
  • metal ions and/or cationic polymers can also be added to the mill whitewater systems prior to the enzyme addition.
  • the disclosed method may be used with any pitch-containing pulp, and especially to pulps with a considerable content of triglycerides and other esters.
  • the addition points of enzyme formulations can be at any one of various locations during the pulping and paper manufacturing processes. Suitable locations include, but are not limited to, latency chest, reject refiner chest, disk filter or Decker feed or accept, whitewater system, pulp stock storage chests (either low density (“LD”), medium consistency (MC), or high consistency (HC)), blend chest, machine chest, headbox, saveall chest, and paper machine whitewater system.
  • LD low density
  • MC medium consistency
  • HC high consistency
  • the effectiveness of the enzyme treatment can be determined by measuring the triglyceride (TG) content in a wood pulp sample at various locations in the pulping and papermaking processes using the triglyceride assay method described in U.S. Pat. No. 7,067,244 by Jiang et al.
  • Metal ions or cationic polymers are added to the stock at a range from 0.025% to 3.0%, and more preferably 0.5-1.2% based on O.D. fibers.
  • Enzyme solutions are added to the stock at the same time or after alum or metal ions addition. Enzyme can be formulated with metal ions and cationic polymers before the enzyme is added to pulp stocks.
  • the dose of the enzyme ranges from 1 to 2000 ppm based on O.D. fibers.
  • the final usage of EnzOx® products is in the range of 0.005% to 0.5%, preferably 0.01% to 0.2% based on O.D. fibers.
  • a newsprint mill TMP pulp stock collected from secondary refiner accept with no alum addition, was collected. Prior to lab tests, it was mixed well to ensure uniformity of the stock. The stock consistency was determined. Based on the consistency, the stock was diluted to 1.0% consistency, and the pH was adjusted to 5.0-5.2. 100 grams of the 1.0% stock was transferred into each of a series of flasks. The flasks containing stock were conditioned in a water bath at the required temperature for 30 minutes with continuous mixing. Alum solution was added to the stock and mixed for 30 seconds and then enzyme solutions were added to the stock. Pulp samples were collected at reaction time of 20 min to 1.5 hours for testing.
  • FIG. 1 shows the TG conversion results without and with 40#/ton and 80#/ton alum using 0.04% EnzOx® A at 65° C.
  • Total TG conversion as well as the rate of conversion was increased by the addition of alum.
  • the rate increase is indicated by higher TG conversion at a much shorter reaction time with alum in comparison with no alum.
  • the stock preparation procedure is the same as in Example 1. Two sets of diluted stocks were prepared and pH values were adjusted to pH4.0, 5.0, 6.0, 7.0, 8.0, 9.0 and 10.0, respectively. One set had no alum, while the other set of was treated with 40 lbs/ton of alum. These stocks were then treated with 0.04% of EnzOx® A for 3 hours. The TG content was measured for pulp samples after the treatment.
  • the pulp stock preparation procedure is the same as in Example 1. Two sets of stocks, one with no alum and the other with 30 lbs/ton alum, were prepared. The stocks were then treated with EnzOx® A at 0.04% based on O.D. fibers at different temperatures from 65 to 85° C. for three hours.
  • the stock preparation procedure is the same as in Example 1. The tests were carried out at high temperatures from 75 to 90° C.
  • EnzOx® B is an enzyme formulation with a thermophilic lipolytic enzyme. Compared to EnzOx® A, EnzOx® B has much higher upper limit of temperature tolerance, as shown in FIGS. 3 and 4 . However, even for this thermophilic enzyme, at temperatures above 80° C., it is quickly deactivated and loses its ability to further hydrolyze TGs. The alum treatment significantly increased the TG conversion even at a higher temperature. Even at 90° C., in the presence of 30#/ton alum, EnzOx® B provides about 40% TG conversion. The alum addition increased the effective working temperature for EnzOx® B by at least 10° C. In other studies, EnzOx® B still showed economically viable TG conversion with alum addition at 95° C., which is about 10-15° C. higher than the optimum temperature for the control enzyme only.
  • the stock preparation procedure is the same as in Example 1.
  • the stocks were treated with the following metal ion solutions which are CaCl 2 , MgCl 2 , FeCl 3 , CuSO 2 and zinc chloride, and ferric chloride.
  • the stock treated with 0.25% metal ions based on O.D. fibers were then treated with EnzOx® A at 65° C. for 3 hours.
  • Two formulations were prepared from Resinase A2X.
  • One experimental product as a control formulation was prepared by dilution with distilled water directly.
  • the other formulation was made by addition a cationic polymer, SUPERFLCO® C573, a polyamine from Cytec Inc. Both formulations were diluted to have about 40% of the original enzyme activity.
  • FIG. 6 shows the relative enzyme activity for the two enzyme formulations when stored at 40° C. for prolonged durations. It can be seen that after 14 and 21 days storage at high temperature of 40° C., the water-only diluted formulation has an enzyme activity of about 75% and 55%, respectively, of the freshly prepared enzymes. This indicates that product loses the enzyme activity quickly at high storage temperatures if no cationic polymer is used. So, in general, the enzyme manufactures require paper mills to store their products preferably in lower than room temperatures. However, this is not always viable in many mill's conditions.
  • Resinase® A2 ⁇ formulation with C573 showed much higher enzyme activity. After 21 days storage at 40° C., the enzyme activities stabilized at around 90% compared with about 55% for the control. Bioactivity tests indicated that the control product had significant microbial growth, while the cationic polymer-stabilized product had no detectable microbial growth. The results demonstrate that the cationic polymers can significantly enhance the shelf life of esterase products.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

Wood pulp is treated with an esterase formulation in combination with a metal ion or cationic polymer to increase the stability or activity or both of esterase enzymes at high temperature, or at extreme pH ranges of acidic and alkaline conditions. The treatment by esterase together with metals ion or cationic polymer can be used to treat pitch containing pulp at high temperatures prior to, during or after refining of wood chip/pulp, in order to enhance the reduction of pitch problems and facilitate in the manufacture of paper.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation of U.S. application Ser. No. 12/349,149, filed Jan. 6, 2009. Application Ser. No. 12/349,149, filed Jan. 6, 2009, is hereby incorporated herein by reference in its entirety.
  • FIELD OF THE INVENTION
  • The present invention is generally in the field of managing wood pitch using enzyme treatment of wood pulp.
  • BACKGROUND OF THE INVENTION
  • Wood resin is composed of fatty acids and resin acids, triglycerides, steryl esters, and sterols. Wood resins, as well as other extractives such as lignins, pectins, and phenols, are the major components of pitch deposits. During mechanical pulping, the encapsulated resin is liberated from ray parenchyma cells and resin canals. Some of the dispersed resin droplets precipitate onto fiber surfaces, impairing fiber to fiber bonding and thereby negatively affecting the physical properties of the pulp. Dispersed resin which precipitates later in the pulping and papermaking processes can affect paper machine runnability and reduce paper quality, resulting in increased manufacturing costs.
  • Traditionally, pitch deposits in pulping and paper manufacturing processes have been reduced by seasoning wood logs and chips, and by the use of physiochemical control agents. For example, cationic coagulant chemicals have been used to fix the extractives to the fibers so that the pitch particles can be removed with the paper products and therefore reduce and/or eliminate the pitch related deposit on the manufacturing equipment. Traditional methods include alum, talc, bentonite, surfactants, pitch stabilizer, detackifiers, and polymers. However, those traditional methods have their limitations due to the complexities of pulping and paper making process, particularly when used with recycled paper.
  • In order to overcome the limitations associated with the use of physiochemical treatments, biological treatments, such as the use of enzymes, have been developed and widely used for pitch control at newsprint mills. For example, lipases have been used to degrade triglycerides into glycerol and fatty acids to reduce the pitch deposition problems caused by triglycerides. Such treatments, however, can result in increased concentrations of certain pitch components and by-products, such as fatty acids, which would affect machine runnability and product quality. In fact, one of the major challenges in modern mills with closed-cycle water systems is the removal of lipophilic wood extractives that tend to accumulate in pulping and papermaking systems or circuits because they can no longer be sufficiently purged from the system via the water. The increasing degree of water closure in mills is leading to an increase in pitch concentrations, which increases the chances of pitch deposition and the discharge of more heavily concentrated pitch-laden waste water. This makes it more difficult for pulp and papermaking mills to meet state and federal requirements for reducing effluents to meet minimum effluent discharge levels.
  • Laccase has been used in some cases to treat pulp, see for example, U.S. Pat. Nos. 5,691,193; 6,242,245; U.S. Pat. No. 6,610,172; and International Publication No. WO 92/09741. Other methods have used enzymes such as lipase and cellulase. U.S. Pat. No. 7,125,471 discloses the use of enzyme compositions containing at least one esterase and at least one lipase for treating sludge added to pulp. U.S. Pat. No. 6,939,437 discloses the use of cationic colloidal alumina microparticles, at least one polymer and optionally a cellulolytic enzyme for the treatment of pulp. U.S. Published Application Nos. 2007/0261806 and 2006/0048908 disclose enzyme formulations for treating pulp (see also U.S. Pat. Nos. 6,770,170; 6,712,933 for additional treatments including enzymes). The treatment pH may be in the range of 3.5 to 12 and the temperature range may be in a range between 35° C. and 90° C. U.S. Pat. No. 5,616,215 discloses the use of lipase and aluminum salt to treat pulp containing mechanical pitch (triglycerides), wherein the treatment pH was in the range of 4-5.5 and the temperature was in the range of 30-70° C.
  • However, many mechanical pulping mills are operated at physical and chemical conditions where current commercially available, “normal” enzymes will be deactivated and lose their functions or activities. For example, thermomechanical pulping (TMP) mills usually are run at temperatures ranging from 70 to 98° C. This temperature range is too high for even what is today known as thermophilic enzymes. Thus the application of normal lipolytic enzymes disclosed in the prior art is limited or even impossible at such high temperatures. At present, the application of “normal” enzymes would require cooling of pulp stocks by addition of cold water, prior to enzyme treatment. The additional cooling creates many problems, for example, temperature shock to the system, increased fresh water usage, and increased demand of a mill's wastewater treatment capacity. The addition of cooling water can cause energy loss in a mill. Most mills have designed their TMP plants with a limited stock storage time. The use of additional cooling water means that the stock will be stored at much lower consistency. This reduces the stock storage time that is badly needed for most mills, because they have to run the TMP plants under the real-time-price (RTP) schedule to manage the energy cost, particularly in summer times. For example, the RTP schedule demands the paper mills to run the TMP only at low energy cost hours, usually from 10 PM to 8 AM, to produce the full day pulp needed for paper machine production. If the stock consistency is lowered, the mill won't have enough storage space to store pulp stocks. Therefore, in many mills, lowering the TMP operating temperature to make the enzyme work is simply not viable.
  • Most tree species, particularly southern pines, have higher contents of extractives in the winter (i.e., the papermaker's “pitch season”) than in the summer. Furthermore, the chemical composition of the winter pitch changes too, that is, there is much higher content of long chain triglycerides (TG) and fatty acids in the tree extractives. Long chain TGs and fatty acids have higher melting points and require high temperatures to remain liquid. TG conversion by lipolytic enzymes is therefore favored thermodynamically at a high temperature. Lipolytic enzymes, being mostly surface-active enzymes, won't work effectively since the TGs and pitch remain solid under temperature ranges where the normal enzymes are active. Additionally, solubility and miscibility of fatty acids and their corresponding salts increase with temperature. High temperature operation helps disperse the pitch in the stock and reduces the risk of forming deposition.
  • It is an object of the present invention to provide a method of treating the fiber stocks with industrial esterases at a temperature 5 to 20 degrees Celsius higher than the enzyme's denaturation temperature.
  • It is an object of the invention to provide a method for decreasing the total amount of extractives in wood pulp that is effective over relatively short treatment times.
  • It is a further object of the present invention to provide an esterase formulation which is stable and active at temperature range from 70 to 98° C.
  • It is a further object of the present invention to provide a method for treating pitch containing pulp at a broad pH 3.0-10.5 with the addition of metal salts, cationic polymers and/or their combinations prior to the treatment using normal industrial esterases.
  • It is still an object of the present invention to provide a method of treating pitch containing pulp at neutral and alkaline pH with an esterase formulation.
  • It is also an object of the present invention to provide a method of treating pitch containing pulp at acidic pH with an esterase formulation.
  • It is also an object of the invention to provide a method of decreasing the total amount of extractives in wood pulp with esterase treatment in order to lower refining energy requirements, and better paper machine runnability.
  • BRIEF SUMMARY OF THE INVENTION
  • A method of treating pitch containing pulp at a higher temperature range than what the esterases allow at normal application temperature or pH has been developed. In one embodiment pitch containing pulp is treated with an effective amount of metal ions selected from the group consisting of aluminum, calcium, magnesium, iron, copper, zinc, titanium and zirconium prior to treatment with a lipolytic enzyme formulation. In another embodiment pitch containing pulp is treated with an effective amount of a cationic polymer. In a more preferred embodiment the pulp is treated with an effective amount of alum. The pulp is treated with an effective amount of a metal ion or cationic polymer effective to increases stability of the enzyme at high temperature and at broad pH ranges of 3-11.
  • The method can be applied to any pitch-containing pulp, such as GW (Ground Wood), TMP (Thermo Mechanical Pulp), CTMP (Chemical Thermo Mechanical Pulp), Recycled ONP (old news paper), and/or their combinations.
  • Examples are pulps produced by mechanical pulping, alone or combined with a certain chemical treatment. The disclosed method enables treatment of pulp with normal a lipolytic enzyme to work at temperature range from about 70° C. to 98° C., preferably from about 70° C. to 90° C.
  • The wood pulp can be treated for a period of time from about 0.1 to 36 hours, more preferably from about 1.0 to about 12 hours. The addition of metal ions or cationic polymers to the pulp prior to enzyme treatment stabilizes the enzyme formulation and speeds up the enzymatic reactions at high temperature and broader pH range. This enhances the effectiveness of the enzyme formulation in removing extractives such as long chain triglycerides whose conversion is favored thermodynamically at high temperatures. Additionally, the ability of the enzyme formulation to be active at high temperatures decreases the need for adding cooling water prior to enzyme treatment, thus reducing the fresh water use and costs associated with waste waster treatment. Furthermore, the ability of the enzyme formulation to be active at lower pH (as low as 3.0) and higher pH (as high as 10.5) reduces the need for acid or base usage for pH adjustment of pulp stocks prior to enzyme treatment. It makes it possible for enzyme to be added to the locations where the conditions can be too harsh for normal lipolytic enzymes with the use of method described herein. In addition, the chemical costs can be reduced.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a graph showing the conversion of triglycerides (TG) using EnzOx® A as a function of reaction time with different amounts of alum (□=0 lbs/ton: ▪=40 lbs/ton and =80 lbs/ton) at 65° C. and pH5.0-5.2.
  • FIG. 2 is a graph showing the conversion of TG using EnzOx® A at different treatment pH without (□=0 lbs/ton) and with (▪=40 lbs/ton) addition of alum at 65° C. and pH5.0-5.2.
  • FIG. 3 is a graph showing the conversion of TG using EnzOx® A at different treatment temperature without (□=0#/ton) and with (▪=30 lbs/ton) addition of alum at pH5.0-5.2.
  • FIG. 4 is a graph showing the conversion of TG using EnzOx® B at different treatment temperature without (□=0 lbs/ton) and with (=30 and ▪=80 #/ton) addition of alum at pH5.0-5.2.
  • FIG. 5 is a graph showing the effect of metal ions on TG conversion using EnzOx® A under normal conditions at 65° C. and pH5.0-5.2.
  • FIG. 6 is a graph showing the relative enzyme activity (compared to the formulation freshly made with water dilution) of formulations (containing EnzOx® A) as a function of storage time under elevated temperature (40° C.), without and with addition of a cationic polymer (Polymer A).
  • DETAILED DESCRIPTION OF THE INVENTION I. Definitions
  • “Pitch”, as used herein, refers to a composition composed of primarily triglycerides (TG), resin acids, fatty acids, waxes, resin esters, fatty alcohols, sterols, and terpenes, which are released from wood fibers during chemical and mechanical pulping processes. These resinous substances usually react with metal ions in the pulp stream and whitewater system which are added by the requirement of mill processes precipitate as aluminum, calcium, and magnesium salts, which may cause problems with the wet end components of paper machines.
  • “Apparent pitch” or “depositable pitch”, as used herein, refers to pitch which is located on the surface of the wood chips or sawdust or wood pulp is suspended in the aqueous phases as dissolved colloidal particles. Apparent pitch content is distinguished from total pitch content or total wood extractives, which includes pitch located on the surface of the wood chips or sawdust or wood pulp as well as pitch encapsulated or trapped within the wood fibers.
  • “Stone ground wood pulp”, as used herein, refers to pulp which is produced by grinding wood or wood chips into relatively short fibers with stone grounding. This pulp is used mainly in newsprint and wood-containing papers, such as lightweight coated (LWC) and super-calendared (SC) papers.
  • “Thermo Mechanical Pulp” or “TMP”, as used herein, refers to pulp that is produced by a thermo-mechanical process where wood chips or sawdust are softened by steam before entering a pressurized refiner. TMP generally has the same end-uses as stone groundwood pulp.
  • “Semi-chemical pulp”, as used herein, refers to pulp produced in a manner similar to TMP but the wood chips and/or sawdust are chemically treated before entering the refiner. This pulp has properties suited to tissue manufacture.
  • “Chemical pulp”, as used herein, refers to pulp produced by the treatment of wood chips or sawdust with chemicals to liberate the cellulose fibers by removing binding agents such as lignin resins and gums. Sulphite and Sulphate pulping, or Kraft, are two types of chemical pulping. Kraft is the predominant pulping process in chemical pulp production.
  • “Recycled pulp” or “recycled fibers” refers to fiber components of a paper or paperboard furnish that is derived from recycled paper and paperboard or wastepaper.
  • II. Materials for Enzymatic Treatment of Wood Pulp
  • A. Esterase and Enzyme Formulations
  • Suitable esterases (EC 3.1.1), include but are not limited to, are phospholipases (EC 3.1.1.32 and EC 3.1.1.4), carboxyl esterases (EC 3.1.1.1), pectinesterase (EC 3.1.1.11), lipolytic enzymes (EC 3.1.1.3) and acetyl esterase (EC 3.1.1.6) or acetyl esterase, which hydrolyze carboxylic esters. Examples of other suitable lipolytic enzymes include cholesterol esterase (EC 3.1.1.13), which hydrolyses sterol esters. Pectin esterase breaks the ester bond linking the pectin groups. Pectin is a family of compounds found in cell walls of plants/trees and has been implicated in problems of drainage and pitch deposition.
  • Mono-, di- and triglycerides in a wood pulp sample can be reduced, i.e. hydrolyzed, in the presence of a lipolytic enzyme, such as a lipase, to form glycerol and fatty acids. Preferably, the lipolytic enzyme is a non-selective lipase (EC 3.1.1.3) that can hydrolyze the ester bonds at all three locations in the glyceride structure. Suitable lipases for the hydrolysis of triglycerides may be derived from plant, animal, or preferably microbial sources. Examples of sources for microbial lipases include Candida rugosa, Rhizopus arrhizus, and Chromobacterium viscosum. Other suitable lipolytic enzymes belong to the family of carboxylic ester hydrolases. Representative examples of these include phospholipases, lipoprotein lipases, and acylglycerol lipases.
  • EnzOx® A, B and C are three of the commercially formulated pitch control products from Enzymatic Deinking Technologies, LLC, Norcross, Ga. 30093. The EnzOx® products contain principally esterases, cellulases, hemicellulase, amylases, and pectinases. In one embodiment, the enzyme formulation is EnzOx® A containing a normal temperature lipase, Resinase® A2X, Novozymes A/S. The working temperature is from 45 to 70° C. with optimum temperature from 55 to 65° C.; the working pH range is from 4.0 to 7.5 with optimum pH range from 4.5 to 6.5. In another embodiment, the enzyme formulation is EnzOx® B, which comprises a commercial thermostable lipolytic enzyme, Resinase® HT, Novozymes A/S. The working temperature range is from 55 to 85° C. with optimum from 65 to 80° C.
  • B. Metal Ions
  • Metal ions that can be used to catalyze the enzymatic reaction of esterases and stabilize the enzyme formulations at high temperature, at alkaline pH, at neutral ph, and at acidic pH conditions include but are not limited to, aluminum, calcium, magnesium, iron, copper, zinc, titanium, and zirconium.
  • The aluminum ion can be provided by any aluminum salt that is soluble or partially soluble under the conditions of the mill processes. In a preferred embodiment, the aluminum ion is provided by Papermaker's alum. Preferably, aluminum sulfate or aluminum chloride is used to provide the aluminum salt.
  • Calcium chloride, magnesium chloride, zinc sulfate, copper sulfate, iron sulfate or chloride, titanium chloride, and zirconium sulfate can also be used.
  • The pitch containing pulp is treated with the metal ions either prior to or together with addition of the enzyme formulation into pulps with sufficient mixing. It is preferred that metals ions are added to the pulp before the enzyme addition. The metal ion or cationic polymer treatment enables EnzOx® A to be active over a temperature range from about 70 to 98° C., more preferably from about 75 to 85° C. instead of optimum range from 55 to 65° C. for the control; and at a pH range from 3.0 to 11, more preferably from about 7 to 10 instead of optimum pH range from 4.5 to 6.5 for the control. The concentration of esterase enzymes used to treat pulp is from 0.005% to 1.0% based on oven dried fibers, preferably 0.005% to about 0.1% based on O.D. fibers. The concentration of the metal ions or cationic polymers is from 1-100 lbs per ton based on oven dried fibers, preferably 10-60 lbs per ton based on O.D. fibers. The addition of the metal ions to wood pulp enables the treatment of wood pulp at higher temperature and wider pH ranges.
  • C. Cationic Polymers
  • Water soluble polymers such as a cationic water soluble polymer can be used to stabilize the enzyme formulation and increase the enzyme's catalytic activity, like the metal ions mentioned above. Examples of such polymers include epichlorohydrin/dimethylamine polymers (EPI-DMA) and cross-linked solutions thereof, polydiallyl dimethyl ammonium chloride (DADMAC), polyethylenimine (PEI), hydrophobically modified polyethylenimine, polyamines, resin amines, polyacrylamide, DADMAC/acrylamide copolymers, and ionene polymers. Examples of ionene polymers include those set forth in U.S. Pat. Nos. 5,681,862, 5,575,993, and 5,256,252. Those above-mentioned polymers can be used in any amount and preferably in dosage ranges from about 0.1-10 lbs per ton based on O.D. fibers, more preferably from 0.5 to 5 lbs/ton based on O.D. fibers.
  • III. Methods of Treatment
  • The enzyme formulations are generally added to the pulp chests, preferably together with metal ions or cationic polymers at a place where sufficient mixing and retention time are available. However, metal ions and/or cationic polymers can also be added to the mill whitewater systems prior to the enzyme addition.
  • The disclosed method may be used with any pitch-containing pulp, and especially to pulps with a considerable content of triglycerides and other esters. The addition points of enzyme formulations can be at any one of various locations during the pulping and paper manufacturing processes. Suitable locations include, but are not limited to, latency chest, reject refiner chest, disk filter or Decker feed or accept, whitewater system, pulp stock storage chests (either low density (“LD”), medium consistency (MC), or high consistency (HC)), blend chest, machine chest, headbox, saveall chest, and paper machine whitewater system.
  • The effectiveness of the enzyme treatment can be determined by measuring the triglyceride (TG) content in a wood pulp sample at various locations in the pulping and papermaking processes using the triglyceride assay method described in U.S. Pat. No. 7,067,244 by Jiang et al.
  • Metal ions or cationic polymers are added to the stock at a range from 0.025% to 3.0%, and more preferably 0.5-1.2% based on O.D. fibers. Enzyme solutions are added to the stock at the same time or after alum or metal ions addition. Enzyme can be formulated with metal ions and cationic polymers before the enzyme is added to pulp stocks. The dose of the enzyme ranges from 1 to 2000 ppm based on O.D. fibers. The final usage of EnzOx® products is in the range of 0.005% to 0.5%, preferably 0.01% to 0.2% based on O.D. fibers.
  • EXAMPLES Example 1 Increased Triglyceride Conversion Kinetics in TMP Pulp
  • Materials and Methods
  • A newsprint mill TMP pulp stock, collected from secondary refiner accept with no alum addition, was collected. Prior to lab tests, it was mixed well to ensure uniformity of the stock. The stock consistency was determined. Based on the consistency, the stock was diluted to 1.0% consistency, and the pH was adjusted to 5.0-5.2. 100 grams of the 1.0% stock was transferred into each of a series of flasks. The flasks containing stock were conditioned in a water bath at the required temperature for 30 minutes with continuous mixing. Alum solution was added to the stock and mixed for 30 seconds and then enzyme solutions were added to the stock. Pulp samples were collected at reaction time of 20 min to 1.5 hours for testing.
  • Results
  • FIG. 1 shows the TG conversion results without and with 40#/ton and 80#/ton alum using 0.04% EnzOx® A at 65° C. Total TG conversion as well as the rate of conversion was increased by the addition of alum. The rate increase is indicated by higher TG conversion at a much shorter reaction time with alum in comparison with no alum.
  • Example 2 Increased TG Conversion at a Broader pH Range by Aluminum Addition
  • Materials and Methods
  • The stock preparation procedure is the same as in Example 1. Two sets of diluted stocks were prepared and pH values were adjusted to pH4.0, 5.0, 6.0, 7.0, 8.0, 9.0 and 10.0, respectively. One set had no alum, while the other set of was treated with 40 lbs/ton of alum. These stocks were then treated with 0.04% of EnzOx® A for 3 hours. The TG content was measured for pulp samples after the treatment.
  • Results
  • The results are given in FIG. 2. The alum treatment clearly increased the TG conversion by EnzOx® A treatment over the entire pH range tested (4-10). Without alum, only moderate TG conversion was obtained in a narrow range of pH 5-6. Above pH=7, there was essentially no apparent enzyme conversion of TG. With 40#/ton alum addition, the TG conversion was increased to 70-80% with alum treatment. This example demonstrated that aluminum ions could stabilize the lipase enzyme activity and catalyze the TG conversion at pH ranges where the enzyme would be inactivated if no alum is present.
  • Example 3 Increased TG Conversion with Alum Treatment at a Higher Temperature Range with EnzOx® a
  • Materials and Methods
  • The pulp stock preparation procedure is the same as in Example 1. Two sets of stocks, one with no alum and the other with 30 lbs/ton alum, were prepared. The stocks were then treated with EnzOx® A at 0.04% based on O.D. fibers at different temperatures from 65 to 85° C. for three hours.
  • Results
  • The results are shown in FIG. 3. Without alum addition, there was no significant TG conversion at above temperature 75° C., indicating that the enzymes were mostly thermally deactivated. In the presence of alum, TG conversion was significantly increased. For instance, at 75° C. TG conversion increased from about 18% without alum to about 82% with 30#/ton alum. It is very obvious that the presence of alum stabilized and protected the enzymes from heat deactivation. The alum addition increased the effective working temperatures for EnzOx® A by about 10° C.
  • Example 4 Increased TG Conversion with Alum Treatment at a Higher Temperature Range with EnzOx® B
  • Materials and Methods
  • The stock preparation procedure is the same as in Example 1. The tests were carried out at high temperatures from 75 to 90° C.
  • Results
  • The results are shown in FIG. 4 after three hours of reaction time.
  • EnzOx® B is an enzyme formulation with a thermophilic lipolytic enzyme. Compared to EnzOx® A, EnzOx® B has much higher upper limit of temperature tolerance, as shown in FIGS. 3 and 4. However, even for this thermophilic enzyme, at temperatures above 80° C., it is quickly deactivated and loses its ability to further hydrolyze TGs. The alum treatment significantly increased the TG conversion even at a higher temperature. Even at 90° C., in the presence of 30#/ton alum, EnzOx® B provides about 40% TG conversion. The alum addition increased the effective working temperature for EnzOx® B by at least 10° C. In other studies, EnzOx® B still showed economically viable TG conversion with alum addition at 95° C., which is about 10-15° C. higher than the optimum temperature for the control enzyme only.
  • Example 5 Increased TG Conversion by Other Metal Ions with EnzOx® a Treatment
  • It is believed that the aluminum effects enzyme stability and activity can also be obtained with other metal ions. This example illustrates the effect of other metal ions on enzyme activity and TG conversion.
  • Materials and Methods
  • The stock preparation procedure is the same as in Example 1. The stocks were treated with the following metal ion solutions which are CaCl2, MgCl2, FeCl3, CuSO2 and zinc chloride, and ferric chloride. The stock treated with 0.25% metal ions based on O.D. fibers were then treated with EnzOx® A at 65° C. for 3 hours.
  • Results
  • The results are shown in FIG. 5. It can be seen that in the presence of various metal ions of Ca, Mg, Zn, Cu and Fe, the TG conversions of pulp stock were all increased by EnzOx® A treatment at 0.04% dosage based on O.D. fibers. The results demonstrated that the metal ions can stabilize the enzyme activity of EnzOx® products and speed up the enzymatic reaction with TG in the pulp.
  • Example 6 Effect of Cationic Polymer on Stability of an EnzOx® a at High Storage Temperature
  • Materials and Methods
  • Most enzymes, when formulated as aqueous solution, experience stability problems, i.e., they lose the enzyme activity quickly. This problem is particularly serious when formulated enzyme products are transported and stored under elevated temperatures (e.g., in the summer). In this example, the commercial Resinase A2X, Novozymes AB, was used to demonstrate the effects of metal ions and cationic polymers on the stability of the enzyme.
  • Two formulations were prepared from Resinase A2X. One experimental product as a control formulation was prepared by dilution with distilled water directly. The other formulation was made by addition a cationic polymer, SUPERFLCO® C573, a polyamine from Cytec Inc. Both formulations were diluted to have about 40% of the original enzyme activity.
  • Results
  • FIG. 6 shows the relative enzyme activity for the two enzyme formulations when stored at 40° C. for prolonged durations. It can be seen that after 14 and 21 days storage at high temperature of 40° C., the water-only diluted formulation has an enzyme activity of about 75% and 55%, respectively, of the freshly prepared enzymes. This indicates that product loses the enzyme activity quickly at high storage temperatures if no cationic polymer is used. So, in general, the enzyme manufactures require paper mills to store their products preferably in lower than room temperatures. However, this is not always viable in many mill's conditions.
  • In contrast with control products that are diluted with water only, Resinase® A2× formulation with C573 showed much higher enzyme activity. After 21 days storage at 40° C., the enzyme activities stabilized at around 90% compared with about 55% for the control. Bioactivity tests indicated that the control product had significant microbial growth, while the cationic polymer-stabilized product had no detectable microbial growth. The results demonstrate that the cationic polymers can significantly enhance the shelf life of esterase products.

Claims (24)

1. A method of enhancing the reduction of pitch deposition or controlling pitch related problems during the pulp and paper making process, the method comprising:
treating pitch-containing pulp stock at a temperature from 80° C. to 98° C. with a first enzyme formulation consisting essentially of one or more esterases (EC 3.1.1),
treating pitch-containing pulp, prior to or during the treatment with the first enzyme formulation, with one or more aluminum salts in an amount effective to stabilize the one or more esterases,
treating pitch-containing pulp, at a temperature below 80° C., with a second enzyme formulation comprising one or more enzymes.
2. The method of claim 1, wherein the esterases are selected from the group consisting of lipase, phospholipases, carboxyl esterases, pectinesterases, and acetyl esterases.
3. The method of claim 1, wherein the application dosage of the enzyme blend is from about 0.005% to 1.0% based on oven-dried fibers.
4. (canceled)
5. The method of claim 1, wherein the salt can be in the form of sulfate, sulfite, chloride, nitrate, perchlorate, phosphate, acetate, or an amino acid.
6. The method of claim 1, wherein the cationic polymer is selected from the group consisting of epichlorohydrin/dimethylamine polymers (EPI-DMA) and cross-linked solutions thereof, polydiallyl dimethyl ammonium chloride (DADMAC), polyethylenimine (PEI), hydrophobically modified polyethylenimine, polyamines, resin amines, polyacrylamide, DADMAC/acrylamide copolymers, and ionene polymers.
7. The method of claim 1, wherein the pitch containing pulp is treated with the first enzyme formulation for a time of from about 0.1 to 36 hours.
8. The method of claim 7 wherein the treatment with the first enzyme formulation is from about 0.5 to 15 hours.
9. (canceled)
10. The method of claim 1 wherein the pitch containing pulp is treated in a location selected from the group consisting of latency chest, pulp storage chests, stock pumps, and white water streams.
11. The method of claim 1 wherein the pitch containing pulp is treated with the enzyme at a pH of between 3.0 and 11 or between 5 and 10.
12. The method of claim 1 wherein the application dosage of the metal ions is from about 0.1% to 10.0%, based on oven-dried fibers.
13. The method of claim 1 wherein the application dosage of the cationic polymer is from about 0.005% to 1.0% based on oven-dried fibers.
14. A composition for enhancing the stability, or activity, or both stability and activity of esterases at elevated temperatures comprising one or more metal salt, a cationic polymer, or both metal salt and cationic polymer, in an amount effective to increase both the enzyme activity and stability.
15. The composition of claim 14, wherein the esterase is selected from the group consisting of lipolytic enzyme, phospholipase, carboxyl esterase, pectinesterase, and acetyl esterase.
16. The composition of claim 13, wherein the metal ion is selected from the group consisting of aluminum, calcium, magnesium, iron, copper, zinc, titanium and zirconium ions.
17. The composition of claim 14, wherein the aluminum ion is in the form of a compound selected from the group consisting of aluminum sulfate, aluminum chloride, poly aluminum sulfate, and sodium aluminate.
18. The composition of claim 14, wherein the cationic polymer is selected from the group consisting of epichlorohydrin/dimethylamine polymers and cross-linked solutions thereof, polydiallyl dimethyl ammonium chloride, polyethylenimine, hydrophobically modified polyethylenimine, polyamines, resin amines, polyacrylamide, DADMAC/acrylamide copolymers, and ionene polymers.
19. The method of claim 1, wherein the second enzyme formulation comprises cellulase, hemicellulase, pectinase, amylase, laccase, or a combination thereof.
20. The method of claim 1, wherein the esterase concentration is from about 0.005% to 1.0% based on oven-dried fibers.
21. The method of claim 20, wherein the esterase concentration is from about 0.01% to 0.5% based on oven-dried fibers.
22. The method of claim 3, wherein the application dosage of the enzyme blend is from 0.01 to 0.5% based on oven-dried fibers.
23. The method of claim 12, wherein the application dosage of the metal ions is from 1% to 5% based on oven-dried fibers.
24. The method of claim 13, wherein the application dosage of the cationic polymer is from 0.01 to 0.5% based on oven-dried fibers.
US14/733,067 2009-01-06 2015-06-08 Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production Abandoned US20150267349A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US14/733,067 US20150267349A1 (en) 2009-01-06 2015-06-08 Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/349,149 US9051692B2 (en) 2009-01-06 2009-01-06 Method of increasing enzyme stability and activity for pulp and paper production
US14/733,067 US20150267349A1 (en) 2009-01-06 2015-06-08 Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US12/349,149 Continuation US9051692B2 (en) 2009-01-06 2009-01-06 Method of increasing enzyme stability and activity for pulp and paper production

Publications (1)

Publication Number Publication Date
US20150267349A1 true US20150267349A1 (en) 2015-09-24

Family

ID=42310955

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/349,149 Expired - Fee Related US9051692B2 (en) 2009-01-06 2009-01-06 Method of increasing enzyme stability and activity for pulp and paper production
US14/733,067 Abandoned US20150267349A1 (en) 2009-01-06 2015-06-08 Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/349,149 Expired - Fee Related US9051692B2 (en) 2009-01-06 2009-01-06 Method of increasing enzyme stability and activity for pulp and paper production

Country Status (1)

Country Link
US (2) US9051692B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030051836A1 (en) * 2001-05-21 2003-03-20 Novozymes A/S Enzymatic hydrolysis of a polymer comprising vinyl acetate monomer
US9051692B2 (en) * 2009-01-06 2015-06-09 Enzymatic Deinking Technologies, L.L.C. Method of increasing enzyme stability and activity for pulp and paper production
CN102985613B (en) * 2010-04-15 2015-11-25 巴克曼实验室国际公司 Use papermaking process and the system of enzyme and cationic accelerant composition
WO2012027272A2 (en) * 2010-08-23 2012-03-01 Hercules Incorporated Method of treating paper forming wire surface
CN110241651A (en) * 2018-12-05 2019-09-17 广东省造纸研究所 A kind of multifunctional compositions and its application improving paper production system
CN112593435B (en) * 2020-12-09 2022-12-23 山东隆科特酶制剂有限公司 Method for improving papermaking quality by alkaline pectinase combined with chemical reagent degumming

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050003516A1 (en) * 2003-04-16 2005-01-06 Novozymes A/S Enzymatic treatment of paper making
US9051692B2 (en) * 2009-01-06 2015-06-09 Enzymatic Deinking Technologies, L.L.C. Method of increasing enzyme stability and activity for pulp and paper production

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2050453B (en) * 1979-05-23 1983-02-09 Tenneco Chem Chemical compositions useful in the manufacture of paper sizing agents
US4964955A (en) * 1988-12-21 1990-10-23 Cyprus Mines Corporation Method of reducing pitch in pulping and papermaking operations
FI905954A (en) 1990-12-03 1992-06-04 Enso Gutzeit Oy FOERFARANDE FOER BLEKNING AV CELLULOSAMASSA.
JPH04240286A (en) * 1991-01-25 1992-08-27 Novo Nordisk As Method for preventing pitch trouble caused by heat resisting lipase
US5616215A (en) * 1991-04-19 1997-04-01 Novo Nordisk A/S Method of making paper from pulp treated with lipase and an aluminum salt
US5256252A (en) * 1992-07-15 1993-10-26 Nalco Chemical Company Method for controlling pitch deposits using lipase and cationic polymer
CA2115881C (en) * 1993-02-25 2000-05-23 Michael G. Paice Non-chlorine bleaching of kraft pulp
US5681862A (en) * 1993-03-05 1997-10-28 Buckman Laboratories International, Inc. Ionene polymers as microbicides
PT731834E (en) * 1993-12-03 2000-09-29 Buckman Labor Inc STABILIZATION OF COPOLYMER ENZYMES ON BLOCK
US5575993A (en) * 1994-08-31 1996-11-19 Buckman Laboratories International, Inc. Ionene polymers containing biologically-active anions
EP0905306A1 (en) * 1997-09-26 1999-03-31 Consortium für elektrochemische Industrie GmbH Multicomponent system for modifying, decomposing or bleaching lignin or lignin-containing materials and method of using this system
US6610172B1 (en) * 1999-05-06 2003-08-26 Novozymes A/S Process for treating pulp with laccase and a mediator to increase paper wet strength
US6939437B1 (en) * 1999-11-19 2005-09-06 Buckman Laboratories International, Inc. Paper making processes using enzyme and polymer combinations
US6770170B2 (en) * 2000-05-16 2004-08-03 Buckman Laboratories International, Inc. Papermaking pulp including retention system
AU6324901A (en) * 2000-05-17 2001-11-26 Buckman Labor Inc Papermaking pulp and flocculant comprising acidic aqueous alumina sol
CN1218087C (en) * 2000-06-16 2005-09-07 巴科曼实验室国际公司 Methods for control of organic contaminants in fiber suspensions
WO2002086230A1 (en) * 2001-04-20 2002-10-31 Enzymatic Deinking Technologies, Llc Rapid triglyceride assay for use in pulp pitch control
US7125471B2 (en) * 2001-11-29 2006-10-24 Buckman Laboratories International, Inc. Papermaking process using enzyme-treated sludge, and products
US20060048908A1 (en) * 2004-09-08 2006-03-09 Enzymatic Deinking Technologies, Llc System for control of stickies in recovered and virgin paper processing
US20070261806A1 (en) * 2006-05-09 2007-11-15 Enzymatic Deinking Technologies, Llc Treatment of Pulp Stocks Using Oxidative Enzymes to Reduce Pitch Deposition
US8308900B2 (en) * 2006-09-15 2012-11-13 Buckman Laboratories International, Inc. Methods to control lipophilic extractives in acacia wood pulp and fiber

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050003516A1 (en) * 2003-04-16 2005-01-06 Novozymes A/S Enzymatic treatment of paper making
US9051692B2 (en) * 2009-01-06 2015-06-09 Enzymatic Deinking Technologies, L.L.C. Method of increasing enzyme stability and activity for pulp and paper production

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
SMOOK, Handbook for Pulp and Paper Technologists, 1992, Angus Wilde Publications, 2nd edition, chapter 14. *

Also Published As

Publication number Publication date
US20100170646A1 (en) 2010-07-08
US9051692B2 (en) 2015-06-09

Similar Documents

Publication Publication Date Title
US20150267349A1 (en) Method of Increasing Enzyme Stability and Activity for Pulp and Paper Production
US20100269989A1 (en) Use of 1,3-selective lipases for pitch control in pulp and paper processes
EP2558640B1 (en) Paper making processes and system using enzyme and cationic coagulant combination
US8048268B2 (en) Method of controlling organic contaminants in pulp and paper making processes
AU2016310398B2 (en) Method for making lignocellulosic paper and paper products
US20070261806A1 (en) Treatment of Pulp Stocks Using Oxidative Enzymes to Reduce Pitch Deposition
CN101680172A (en) Methods to control organic contaminants in fibers
CA2862248A1 (en) Enzymatic pre-treatment of market pulp to improve fiber drainage and physical properties
JPH06173192A (en) Method for suppressing deposition of pitch in pulp manufacturing and paper manufacturing process
US20050000666A1 (en) Use of hemicellulase composition in mechanical pulp production
EP1454014B1 (en) Papermaking process using enzyme-treated sludge, and products
US20070062654A1 (en) Treatment of wood chips using enzymes
US5667634A (en) Method for controlling pitch deposits in papermaking process using lipase and polyelectrolyte
JP3149952B2 (en) Lipase-catalyzed ester hydrolysis
WO2013165568A1 (en) Pulp fiber modification using expansin or swollenin in combinations with one or more enzymes

Legal Events

Date Code Title Description
AS Assignment

Owner name: ENZYMATIC DEINKING TECHNOLOGIES, L.L.C., GEORGIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WANG, XIANG H.;MA, JIAN HUA;JIANG, CHENGLIANG;AND OTHERS;REEL/FRAME:035852/0459

Effective date: 20090109

STCV Information on status: appeal procedure

Free format text: ON APPEAL -- AWAITING DECISION BY THE BOARD OF APPEALS

STCV Information on status: appeal procedure

Free format text: BOARD OF APPEALS DECISION RENDERED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- AFTER EXAMINER'S ANSWER OR BOARD OF APPEALS DECISION