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WO2008112534A2 - Utilisation de borates d'ammonium quaternaire en tant que biocides antifongiques, anti-mildiou, anti-moisissure pour le traitement de pâte et de papier à papier - Google Patents

Utilisation de borates d'ammonium quaternaire en tant que biocides antifongiques, anti-mildiou, anti-moisissure pour le traitement de pâte et de papier à papier Download PDF

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Publication number
WO2008112534A2
WO2008112534A2 PCT/US2008/056186 US2008056186W WO2008112534A2 WO 2008112534 A2 WO2008112534 A2 WO 2008112534A2 US 2008056186 W US2008056186 W US 2008056186W WO 2008112534 A2 WO2008112534 A2 WO 2008112534A2
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WO
WIPO (PCT)
Prior art keywords
substituted
groups
quaternary ammonium
paper
range
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Application number
PCT/US2008/056186
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English (en)
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WO2008112534A3 (fr
Inventor
Joe D. Sauer
George W. Cook
William S. Pickrell
Christopher J. Nalepa
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Albemarle Corporation
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.)
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Publication date
Application filed by Albemarle Corporation filed Critical Albemarle Corporation
Publication of WO2008112534A2 publication Critical patent/WO2008112534A2/fr
Publication of WO2008112534A3 publication Critical patent/WO2008112534A3/fr

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Classifications

    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP 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
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03—Non-macromolecular organic compounds
    • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/07—Nitrogen-containing compounds
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP 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
    • D21H21/00—Non-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
    • D21H21/14—Non-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 characterised by function or properties in or on the paper
    • D21H21/36—Biocidal agents, e.g. fungicidal, bactericidal, insecticidal agents

Definitions

  • the present invention relates to a method of controlling mold, fungus, and/or mildew in pulp and/or paper processing. More particularly, the present invention relates to the use of quaternary ammonium borate compositions as biocides and/or paper additives in pulp and paper processing.
  • Paper manufacturing generally involves a series of processes that can be roughly grouped into five major manufacturing categories, 1) pulp production, 2) pulp processing and the recovery of chemicals used during pulp processing, 3) pulp bleaching, if a white paper is the desired end product, 4) refining or preparation of the stock used to produce paper, and 5) the manufacturing of a paper product.
  • biocidial agents are used to control the growth of many microorganisms because the growth or presence of these microorganisms is detrimental to the paper manufacturing process. For example, the presence of these microorganisms can cause increased sheet breaks, wet-end depositions, and increased usage of various additives used in the papermaking process.
  • oxidizing agents have been used to control microorganisms in the papermaking process. While the use of these oxidizer such as sodium hypochlorite can be effective, by their very nature, oxidizing compounds are not persistent, and are "spent” or “consumed” in a rapid fashion, leaving the system unprotected with regard to biocidal action. In the paper industry this is especially the case because of the presence of organic materials such as fiber, starch, etc. materials in the process. Typically, these organic materials react with and consume the oxidizer, making it much less effective at controlling microbial populations. Thus, it has been common practice to overdose the paper syatem with oxidizing biocides, which suffers from its own drawbacks. For example, the overdosing of oxidizers can cause an increased usage of wet-end chemicals such as sizing agents along with higher corrosion rates and reduced felt life.
  • the present invention relates to the use of quaternary ammonium borate compositions as a biocide in the manufacturing of paper products.
  • Quaternary ammonium borate compositions suitable for this purpose include quaternary ammonium compounds having the formula: wherein Y is selected from H 2 BO 3 ' ; HBO 3 "2 ; BO 3 '3 ; B 4 O 7 “2 ; HB 4 O 7 “ ; B 3 O 5 " ; B 5 O 8 '2 ; and BO 2 " ; R 1 , R 2 , R 3 and R 4 are independently selected from /) substituted or unsubstituted alkyl groups or //) substituted or unsubstituted alkenyl groups, wherein if i) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups; and m
  • Y is a borate counter-anion and m can be 1, 2, 3, 4, or 5, depending on the selection of Y.
  • Borate anions suitable for use herein include the dihydrogen borate anion, H 2 BO 3 " ; the hydrogen borate anion, HBO 3 "2 ; the borate anion, BO 3 "3 ; the tetraborate anion, B 4 O 7 “2 ; the hydrogen tetraborate anion, HB 4 ⁇ 7 " ; B 3 Os " ; pentaborate, B 5 Os “2 ; and BO 2 " .
  • Y is suitably selected from H 2 BO 3 " ; HBO 3 '2 ; BO 3 “3 ; B 4 O 7 “2 ; HB 4 O 7 “ ; B 3 O 5 “ ; B 5 O 8 “2 ; and BO 2 " . It is preferred that Y is BO 3 "3 , and m is 3.
  • the four carbon chains, i.e. R 1 , R 2 , R 3 and R 4 , of the quats used in the present invention are independently selected from /) substituted or unsubstituted alkyl groups or H) substituted or unsubstituted alkenyl groups, wherein if / ' ) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • Alkyl and alkenyl groups suitable for use in the quats are those that contain in the range of from 1 to 20 carbon atoms.
  • Ri and R 2 are independently chosen from alkyl groups having in the range of from 1 to 3 carbon atoms
  • R 3 and R 4 are independently chosen in the range of from 6 to 20 carbon atom-containing groups selected from i) substituted or unsubstituted alkyl groups or H) substituted or unsubstituted alkenyl groups, wherein if / ' ) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups; and m is 1, 2, or 3.
  • Rj and R 2 are methyl groups and R 3 and R 4 are independently selected from unsubstituted alkyl groups containing in the range of from 8 to 14 carbon atoms.
  • one of R 3 or R 4 is an unsubstituted alkyl group containing in the range of from 8 to 10 carbon atoms
  • one of R 3 or R 4 is an unsubstituted alkyl group containing in the range of from 12 to 14 carbon atoms.
  • At least one, sometimes only one and in other embodiments only two, of the four carbon chains, i.e. Ri, R 2 , R 3 and R 4 is selected from i) substituted or unsubstituted alkyl groups that contain from 13 to 16, sometimes 14 to 16, sometimes 14, carbon atoms or U) substituted or unsubstituted alkenyl groups that contain from 13 to 16, sometimes 14 to 16, sometimes 14, carbon atoms, wherein if /) or U) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • These carbon chains can be saturated or unsaturated, preferably unsubstituted.
  • at least two, in some embodiments only two, and in other embodiments three, of Ri, R 2 , R 3 and R 4 are independently chosen from alkyl groups having from 1 to 4, sometimes 1 to 3, in some embodiments 2 to 4, carbon atoms.
  • one of Ri, R 2 , R 3 and R 4 be selected from ⁇ ) substituted or unsubstituted alkyl groups or if) substituted or unsubstituted alkenyl groups, wherein if i) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • the alkyl and alkenyl groups are those that contain from 1 to 20 carbon atoms.
  • the one of Ri, R 2 , R 3 and R 4 is chosen from 6 to 20 carbon atom-containing groups selected from i) substituted or unsubstituted alkyl groups or U) substituted or unsubstituted alkenyl groups, wherein if /) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups; and m is 1, 2, 3, 4, or 5, sometimes 1, 2, or 3.
  • it is selected from unsubstituted alkyl groups containing from 8 to 14 carbon atoms.
  • it is selected from unsubstituted alkyl group containing from 8 to 10 carbon atoms
  • it is selected from unsubstituted alkyl groups containing from 12 to 14 carbon atoms.
  • At least two of the four carbon chains be independently selected chosen from alkyl groups having from 1 to 4, sometimes 1 to 3, in some embodiments 2 to 4, carbon atoms, and two of the four carbon chains be independently chosen from 6 to 20 carbon atom-containing groups selected from /) substituted or unsubstituted alkyl groups or if) substituted or unsubstituted alkenyl groups, wherein if /) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups; and m is 1, 2, 3, 4, or 5, sometimes 1, 2, or 3, wherein ranges as described above are contemplated and the two of the four carbon chains independently chosen from 6 to 20 carbon atom-containing groups contain different numbers of carbon atoms.
  • At least one, sometimes only one and in other embodiments only two, of the four carbon chains, i.e. Ri, R 2 , R 3 and R 4 is selected from i) substituted or unsubstituted alkyl groups that contain from 13 to 16, preferably 14 to 16, more preferably 14, carbon atoms or H) substituted or unsubstituted alkenyl groups that contain from 13 to 16, preferably 14 to 16, more preferably 14, carbon atoms, wherein if /) or H) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • These carbon chains can be saturated or unsaturated, preferably unsubstituted.
  • at least two, in some embodiments only two, and in other embodiments three, Of R 1 , R 2 , R 3 and R 4 are independently chosen from alkyl groups having from 1 to 4, preferably 1 to 3, in some embodiments 2 to 4, carbon atoms.
  • one of Ri, R 2 , R 3 and R 4 be selected from / ' ) substituted or unsubstituted alkyl groups or if) substituted or unsubstituted alkenyl groups, wherein if / ' ) or if) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • the alkyl and alkenyl groups are those that contain from 1 to 20 carbon atoms.
  • the one of Ri, R 2 , R3 and R 4 is chosen from 6 to 20 carbon atom-containing groups selected from ⁇ ) substituted or unsubstituted alkyl groups or H) substituted or unsubstituted alkenyl groups, wherein if i) or U) is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups; and m is 1, 2, or 3.
  • it is selected from unsubstituted alkyl groups containing from 8 to 14 carbon atoms.
  • it is selected from unsubstituted alkyl group containing from 8 to 10 carbon atoms
  • it is selected from unsubstituted alkyl groups containing from 12 to 14 carbon atoms.
  • m is 2, and one of the four organic radicals of a quat may be a "shared" radical with a second quat.
  • R 4 is shown as the shared radical, the shared radical can be any of Ri, R 2 , R3, or R 4 .
  • the quaternary ammonium compounds used in the practice of the present invention have the general formula:
  • R 1 , R 2 , R 3 , R 4 are as described above including preferred embodiments, and Y is selected from those anions described above having an ionic charge of -2, in some embodiments a borate anion having an ionic charge of -2, in some embodiments,
  • R 1 , R 2 , R 3 , R 4 are as described above including preferred embodiments, and each Y is independently selected from borate anions having an ionic charge of -1, in other embodiments each Y is H 2 BO 3 " . It should be noted that while in this embodiment R 4 is shown as the shared radical, the shared radical can be any of Rj, R 2 , R 3 , or R 4 .
  • m is 3, and one of the four organic radicals of a quat is a "shared" radical with a second quat.
  • the quaternary ammonium compounds used in the coating formulations of the present invention can have the general formula:
  • Ri, R 2 , R 3 , and R 4 are as described herein including preferred embodiments, and one Y is independently selected from the borate counter-anions described above having an ionic charge of -2 and the other Y is selected from borate counter-anions having an ionic charge of -1.
  • one Y is selected from H 2 BO 3 " ; HB 4 O 7 " ; B 3 O 5 " ; and BO 2 " and the other Y is selected from HBO 3 "2 ; B 4 O 7 "2 ; and B 5 O 8 "2 .
  • R 4 is shown as the shared radical, the shared radical can be any of R 1 , R 2 , R 3 , or R 4 .
  • Ri, R 2 , R 3 , and R 4 are as described above including preferred embodiments, and each Y is independently selected from those borate counter anions having a net ionic charge of -1. In some embdoiments, each Y is independently selected from H 2 BO 3 " ; HB 4 O 7 " ; B 3 (V. It should be noted that while in this embodiment R 4 is shown as the shared radical, the shared radical can be any of Rj, R 2 , R 3 , or R 4 .
  • m is 3 and Y is BO 3 "3 .
  • the quaternary ammonium compounds used in the present invention have the general formula:
  • R 1 , R 2 , R 3 , or R 4 are as described above including preferred embodiments. It should be noted that while in this embodiment R 4 and R 2 are shown as the shared radicals, the shared radicals can be independently any of Ri, R 2 , R 3 , or R 4 or any combinations thereof.
  • R 4 and R] can be the shared radicals, Ri and R 3 can be the shared radicals, etc.
  • all three nitrogen atoms can share the same radical group, independently selected from Rj, R 2 , R 3 , or R 4 .
  • one, in some embodiments more than one, quaternary ammonium compound(s) having the formula can be used:
  • R 1 , R 2 , R 3 , Y, and m are as described above, R' is a hydrocarbon group having from 1-10 carbon atoms, in some embodiments in the range of from 1 to 5, in some embodiments in the range of from 1 to 3, and R" and R'" are independently selected from i) substituted or unsubstituted alkyl groups or U) substituted or unsubstituted alkenyl groups, wherein if / ' ) or / ' 0 is substituted, they have one or more substituent groups selected from aryl, heterocyclyl, hydroxyl, ester, benzyl, carboxyl, halo, nitro, cyano, alkoxy or oxo groups.
  • R" and R'" are selected from unsubstituted alkyl groups having in the range of from 1 to 20 carbon atoms, in some embodiments in the range of from 1 to 15, and in other embodiments in the range of from 6 to 14.
  • the quats of the present invention can be prepared by any methods known in the art, exemplary methods include those described in commonly-owned co-pending applications PCT US2005/010162 and US 60/730,821, which are incorporated herein by reference in their entirety.
  • the processes used in the production of quats typically produce quats in an aqueous solution.
  • the aqueous solution typically comprises water, at least one polar organic co-solvent, and one or more quats, as described herein.
  • These aqueous solutions generally have a polar organic co-solvent to water ratio in the range of from about 10:90 up to about 99:1 (wt. co-solvent: wt. water based on the combination of the water and polar organic co-solvent), and the exact amount of the polar organic co-solvent and water is selected according to the selection of Ri, R 2 , R 3 and R 4 .
  • the ratio of co-solvent : water, by weight and on the same basis is within the range of from about 50:50 to about 99:1, about 60:40 to about 99:1 is more preferred, about 70:30 to about 98:2 is even more preferred, and about 80:20 to about 95:5 is yet more preferred.
  • aqueous solutions having a higher ratio of co-solvent to water are preferred for quats containing very hydrophobic alkyl substituent groups, e.g., double tailed or twin tailed quats where the alkyl groups are Ci 0 - C 20 , for example, while aqueous solutions having a lower ratio of co-solvent to water are preferred for boron-quats having less hydrophobic alkyl substituent groups, e.g., a (C 2 - C 6 ) alkyltrimethylammonium salt.
  • the aqueous solutions comprise water, at least one polar organic co-solvent and the quat(s) according to the present invention.
  • these ratios were based on the amount of polar organic co-solvent and water.
  • the mixture is a ternary composition comprising at least three major components, water, polar organic co-solvent, and the quat "salt".
  • the ratio of the components of the aqueous solution can be represented as a ratio of wt. quat: wt. polar organic co-solvent: wt.
  • an aqueous solution formed by adding 25% by weight of a quat salt to a mixture comprising an 85:15 by weight mixture of methanol: water would have a ternary composition, by weight, of 25:64:11, quat salt: methanol: water by weight, based on the aqueous solution.
  • aqueous solutions generally have a concentration of quat(s) ranging from about 1 to about 50 wt.% quat, based on the aqueous solution.
  • the quaternary ammonium betaine compositions are contained in an aqueous solution, as described above.
  • the aqueous solutions are metal coupler free.
  • metal coupler free it is meant that the aqueous solutions do not contain metals such as copper, mercury, lead, cadmium, hexavalent chromium, arsenic, antimony, or zinc. These metals are commonly used for their biocidal properties. However, these and other "heavy" metals pose certain environmental concerns, thus, it would be beneficial to use biocides without these heavy metals.
  • the quaternary ammonium borate compositions can be used as a biocide in any step of the papermaking process.
  • the quaternary ammonium borate compositions can be used as an effective biocide in the pulping area or in the wet end.
  • the quaternary ammonium borate compositions of the present invention can also be applied to the paper sheet to provide the end paper product with desired characteristics, discussed below.
  • the quaternary ammonium borate compositions can be applied to the paper sheet at the size press.
  • the quaternary ammonium borate compositions can be applied to the paper sheet and used as a biocide in the wet end and/or in the pulping process.
  • the inventors hereof while not wishing to be bound by theory, believe that the application of quaternary ammonium borates to the paper sheet or use of the same in the wet end can impart at least one of, preferably at least two of, more preferably substantially all of, the following properties to the final paper product: i)fungicidal properties, ii)mildewcidal properties, iii)biocidal properties, and iv) termite repellant properties.
  • the quats of the present invention are effective at imparting some flame retardant properties to the treated paper.
  • “some flame retardant properties” it is meant that the paper containing the quaternary ammonium borate compositions does not ignite, and or burn when exposed to flame, as readily as paper that does not contain the quaternary ammonium borate compositions.
  • repelling termites it is meant that the termites do not feed on the quat treated paper, will crawl across the quat-treated paper without feeding on it, and in essence resort to cannibalistic behavior for food instead of feeding on the quat treated paper.
  • the inventors hereof while not wishing to be bound by theory, believe that the termites do not recognize the paper as a food source.
  • the final paper product comprises an effective amount of the quaternary ammonium borate composition.
  • an effective amount it is meant that the treated paper comprises in the range of from about 1 to about 30 wt.%, based on the weight of the treated paper sheet, of the quaternary ammonium borate composition. In preferred embodiments, the treated paper comprises from about 5 to about 10 wt.% of the quaternary ammonium borate composition, on the same basis.
  • the quat is used as a biocide in he papermaking process, it is added until an effective mount of quat is present in the area where biocidial activity is desired.
  • the amount of quat added is that amount necessary to provide for a quat concentration in the range of from about 10,000 to about 300,000 ppm of the quat is present in the white water, preferably in the range of from about 50,000 to about 100,000 ppm.
  • the amount of quat present in the pulp storage chest is added is in the range of from about 10,000 to about 300,000 ppm of the quat is present in the chest, preferably in the range of from about 50,000 to about 100,000 ppm.
  • the amount of quat added is that amlount necessary to maintain a quat concentration in the range of from about 10,000 to about 300,000 ppm of the quat, preferably in the range of from about 50,000 to about 100,000 ppm. It should be noted that it is within the present invention to add the quaternary ammonium composition either batch-wise or continuously to maintain a satisfactory concentration of quat. However, it is preferred that the quat be continuously metered to maintain the concentration of quat. [0033] The above description is directed to several embodiments of the present invention. Those skilled in the art will recognize that other embodiments, which are equally effective, could be devised for carrying out the spirit of this invention. It should also be noted that preferred embodiments of the present invention contemplate that all ranges discussed herein include ranges from any lower amount to any higher amount.

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  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Paper (AREA)

Abstract

La présente invention concerne l'utilisation de compositions à base de borate d'ammonium quaternaire en tant que biocides et/ou additifs de papier dans le traitement de pâte à papier et/ou de papier.
PCT/US2008/056186 2007-03-09 2008-03-07 Utilisation de borates d'ammonium quaternaire en tant que biocides antifongiques, anti-mildiou, anti-moisissure pour le traitement de pâte et de papier à papier WO2008112534A2 (fr)

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US89391307P 2007-03-09 2007-03-09
US60/893,913 2007-03-09

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WO2008112534A2 true WO2008112534A2 (fr) 2008-09-18
WO2008112534A3 WO2008112534A3 (fr) 2008-11-06

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105926353A (zh) * 2016-06-12 2016-09-07 铜陵锋帆彩色印务有限公司 凹凸棒土改性的防霉纸板及其制备方法
CN106087570A (zh) * 2016-06-12 2016-11-09 铜陵锋帆彩色印务有限公司 基于高岭土改性的防霉纸板涂料及其制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4970201A (en) * 1988-08-16 1990-11-13 Rutgerswerke Ag Preservatives for cellulose containing products
WO2005097729A2 (fr) * 2004-03-26 2005-10-20 Albemarle Corporation Procede de synthese de composes d'ammonium quaternaire et compositions associees
US20060257578A1 (en) * 2003-04-09 2006-11-16 Jun Zhang Micronized wood preservative formulations comprising boron compounds

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4970201A (en) * 1988-08-16 1990-11-13 Rutgerswerke Ag Preservatives for cellulose containing products
US20060257578A1 (en) * 2003-04-09 2006-11-16 Jun Zhang Micronized wood preservative formulations comprising boron compounds
WO2005097729A2 (fr) * 2004-03-26 2005-10-20 Albemarle Corporation Procede de synthese de composes d'ammonium quaternaire et compositions associees

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105926353A (zh) * 2016-06-12 2016-09-07 铜陵锋帆彩色印务有限公司 凹凸棒土改性的防霉纸板及其制备方法
CN106087570A (zh) * 2016-06-12 2016-11-09 铜陵锋帆彩色印务有限公司 基于高岭土改性的防霉纸板涂料及其制备方法

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