US2707144A - Method of bleaching mechanically disintegrated wood pulp - Google Patents
Method of bleaching mechanically disintegrated wood pulp Download PDFInfo
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- US2707144A US2707144A US240982A US24098251A US2707144A US 2707144 A US2707144 A US 2707144A US 240982 A US240982 A US 240982A US 24098251 A US24098251 A US 24098251A US 2707144 A US2707144 A US 2707144A
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- pulp
- hydrosulphite
- polyphosphate
- bleaching
- wood pulp
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1026—Other features in bleaching processes
- D21C9/1042—Use of chelating agents
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/06—Chelate
Definitions
- the present invention relates to an improved process for bleaching wood pulp, and more particularly it relates to an improved process for bleaching mechanically-disintegrated wood pulp involving the use of a water-soluble hydrosulphite in conjunction with an agent providing a markedly-improved bleach.
- the bleaching of Wood pulp particularly mechanically-disintegrated wood pulp
- One of the bleaching agents which have been suggested for this purpose is a water-soluble hydrosulphite.
- a hydrosulphite By the use of a hydrosulphite, the brightness of mechanically-disintegrated wood pulp, which is normally in the neighborhood of about 60% when measured by the General Electric Reflectance Meter, can be increased a few points at the most. Attempts have been made to increase this bleaching effect through the use of pH control, temperature control, buffering agents, whitening agents, and the like. However, no substantial improvements resulted from these attempts.
- Another object of the present invention is to provide an improved method for bleaching mechanically-disintegrated wood pulp involving the use of a water-soluble hydrosulphite wherein the brightness increase realized is markedly greater than that obtained through prior methods involving the use of a hydrosulphite.
- Still another object of the present invention is to provide a simple method for bleaching mechanicallydisintegrated wood pulp involving the use of a watersoluble hydrosulphite in conjunction with another agent, whereby the brightness increase obtained is substantially greater than that obtained through the use of a watersoluble hydrosulphite alone.
- the bleaching process of the present invention comprises intimately mixing, with mechanically-disintegrated wood pulp at an elevated temperature, a water-soluble hydrosulphite and a water-soluble polyphosphate.
- the polyphosphate will be mixed with the pulp at a time not substantially later than that at which the hydrosulphite is mixed with the pulp, and preferably the hydrosulphite and polyphosphate are mixed substantially simultaneously with the wood pulp.
- the hydrosulphite and polyphosphate are left in contact with the pulp until the desired bleaching is obtained.
- the polyphosphate must be incorporated in the wood pulp not substantially later than the time at which the hydrosulphite is mixed with the wood pulp. Regardless of the theory, it is a fact that the incorporation of the polyphosphate with the hydrosulphite in the wood pulp results in a marked improvement in the bleaching etfect realized from the hydrosulphite.
- mechanically-disintegrated wood pulp contains a relatively high concentration of lignins which often react with certain of the metal ions, particularly iron, to form highly coloring products.
- the combining of the polyphosphate with the stated metal ions thus also prevents the metal ions from combining with the lignin accounting for a further increase in brightness.
- Wood pulp treated in accordance with the present invention it is, as stated, mechanically-disintegrated wood pulp.
- Wood pulp there are two types of such Wood pulp: (1) ground wood pulp and (2) semichemical wood pulp.
- Ground wood pulp as is well-known, is obtained merely by grinding logs to reduce the logs to fibers.
- Semi-chemical wood pulp is obtained by first reducing the log to chips, treating the chips briefly with chemicals. such as sodium sulphite and sodium bicarbonate, at elevated temperature and pressure preliminarily to soften the chips somewhat, and grinding the chips to fibers.
- chemicals such as sodium sulphite and sodium bicarbonate
- the pulp treated in accordance with the present invention may be obtained from several different sources. That is to say it may be ground wood pulp or semi-chemical pulp coming directly from the grinder, or from a point in the pulp-processing procedure remote from the grinder. On the other hand, the pulp coming from the grinder may be first dried and baled, and the bales shipped to a distant point where they are broken up and re-pulped. The pulp treated in accordance with the present invention may be such re-pulped material.
- the source of the pulp treated in accordance with the present invention is relatively immaterial so long as during the bleaching process it has the proper consistency.
- the consistency of the pulp treated in accordance with the present process will be at least about 0.5%, by weight, and the con sistency thereof may range up to the point where satisfactory mixing is not feasible, for example up to 10%, or even 15%, by weight, if desired.
- the consistency of pulp is between about 2% and about 5%, by weight.
- both the pulp coming directly from the grinder and the re-pulped material will have a consistency within these ranges.
- the consistency of pulp obtained from other points in the pulp-processing treatment may require adjustment, and, if such be the case, the consistency of the pulp can be adjusted to the desired level by simply adding or removing water.
- the treatment in accordance with the present invention is at an elevated temperature. That is to say, the temperature of the pulp during the treatment :will be above normal room temperature, and generally will be above about F., more generally above about F. While the temperature of the pulp may range as high as 212 F., no advantage is to be gained by operating at such temperatures, and a preferred operating range is between about and about F. The provision of the stated temperatures will ofier no problem to those skilled in the art. In the event fresh ground wood pulp, that is the slurry coming directly from the grinder, is being treagad, such pulp will generally be at a satisfactory temperature due to the heat generated during the grinding operation.
- a water-soluble hydrosulphite as the main bleaching agent.
- Watersoluble hydrosulphites employed for bleaching wood pulp are well-known and include zinc hydrosulphite, the alkali metal hydrosulphites, such as sodium hydrosulphite and potassium hydrosulphite, ammonium hydrosulphite, and the like. Of the various water-soluble hydrosulphites, sodium hydrosulphite and zinc hydrosulphite, particularly the former, are preferred.
- the hydrosulphite may be added to the pulp in solid form or as a solution in water.
- the hydrosulphite first be dissolved in water and the resulting solution then mixed with the pulp.
- the amount of hydrosulphite incorporated in the pulp may vary somewhat depending upon the type of pulp treated, the degree of brightness increase desired, and other factors known to those skilled in the bleaching art. Generally, the amount of hydrosulphite mixed with the pulp will be at least about 0.25 by weight, based on the weight of the dry pulp. While amounts of hydrosulphite as high as about 5% or even higher, may be employed, no significant advantage is to be gained by using amounts substantially in excess of about 3%, by weight. Preferably, the amount of hydrosulphite employed will be between about 0.5% and about 1.5%, by weight, based on the dry weight of the pulp.
- polyphosphate employed in accordance with the present process it will, as stated, be any of the water-soluble polyphosphates, that is, a polyphosphate having the formula (M2O)P2O5 wherein M is a monovalent cation providing water-solubility to the compound and wherein x is less than 3.
- M is a monovalent cation providing water-solubility to the compound and wherein x is less than 3.
- monovalent cations providing water-solubility to the compound are hydrogen, NH4, the alkali metals, such as sodium and potassium, and the like.
- Mixtures of polyphosphates may be employed if desired.
- the polyphosphate employed may be of the crystalline type or of the glassy type.
- polyphosphates that may be employed in accordance with the present invention (using sodium for M for the purpose of illustration) are sodium pyrophosphate (Na4P2O7) wherein x is 2, sodium tetraphosphate (NaePrOm) wherein x is 1.5, sodium tripolyphosphate (NaaPsOro) wherein x is 1.67, sodium hexapolyphosphate (NasPsOrs) wherein x is 1.33, sodium heptapolyphosphate (Na9P'zO22) wherein x is 1.29, sodium decapolyphosphate (NamPmOar) wherein x is 1.2, and the like.
- Na4P2O7 sodium tetraphosphate
- NaePrOm sodium tripolyphosphate
- NaaPsOro sodium tripolyphosphate
- NasPsOrs sodium hexapolyphosphate
- Na9P'zO22 sodium heptapolyphosphate
- polyphosphates mentioned those in which x in the above formula is between about 1 and about 2, and particularly where M is an alkali metal, especially sodium, are preferred.
- M is an alkali metal, especially sodium
- sodium tetraphosphate and sodium pyrophosphate, especially the former may be mentioned.
- the polyphosphate may be added to the wood pulp as a solid or as an aqueous solution thereof, preferably the latter.
- the amount of polyphosphate employed may vary somewhat depending upon the type of pulp treated and the degree of brightness increase desired. In most cases the amount of polyphosphate employed will be at least about 0.1%, by weight, based on the weight of the dry pulp. While amounts of polyphosphate as high as about 5% or even higher, may be employed, no significant advantage is to be gained by the use of amounts of polyphosphate substantially in excess of about 23%. Preferably, the amount of polyphosphate employed is between about 0.3% and about 1%, by weight, based on the weight of the dry pulp.
- the polyphosphate will be added to the pulp not substantially later than the time when the hydrosulphite is added to the pulp.
- the polyphosphate may be added to the pulp at any time before, or at the same time as the hydrosulphite is added thereto, or may even be added directly after the hydrosulphite is added to the pulp.
- the term not substantially later when used in connection with the time of addition of the polyphosphate to the pulp in relation to the time of addition of the hydrosulphite means that any delay between the addition of the hydrosulphite to the pulp and the addition of the polyphosphate to the pulp will not be such as will permit a substantial amount of the hydrosulphite to be decomposed before the polyphosphate is mixed therewith.
- the polyphosphate and the hydrosulphite are preferably mixed substantially simultaneously with the wood pulp.
- the hydrosulphite and the polyphosphate may be added separately but substantially simultaneously, or the hydrosulphite and the polyphosphate may be premixed, for example, in water, and the resulting mixture added to the pulp. This latter means is the preferred Way of incorporating and mixing the hydrosulphite and polyphosphate with the wood pulp.
- the hydrosulphite and polyphosphate must be intimately mixed with the wood pulp. This intimate mixture may be obtained through a wide variety of means, such as the use of conventional mixing blades, and the like. Following mixing, the hydrosulphite and polyphosphate are permitted to remain in contact with the pulp until the desired bleaching has taken place. This time of contact may be varied depending upon the amounts of hydrosulphite and of polyphosphate employed, the temperature conditions employed, the type of pulp treated, the degree of brightness desired, as well as the other considerations known to those skilled in the bleaching art. However, in general, the time may range from as little as a few minutes, for example three minutes, up to an hour and a half or even longer. Under the preferred operating conditions referred to above, satisfactory bleaching may be obtained in from about 10 to about 30 minutes.
- the pH of the mixture during the process should not be permitted to become substantially alkaline, that is to say, the pH of the medium during the bleaching treatment should not be substantially in excess of about 8.5.
- a pH on the acid side of neutrality may be, and preferably is, employed, and a pH as low as about 3 is satisfactory.
- the precise pH employed will depend somewhat upon the nature of the hydrosulphite and polyphosphate selected, for example, when the polyphosphate is an alkali metal salt, the pH may be somewhat higher than when the cation is one of the other mentioned materials. In most cases, the pH will range between about 4 and about 6.5, with pI-Is between about 5 and about 6 being preferred.
- the adjustment of the pH if after the addition of the hydrosulphite and polyphosphate such adjustment is desired, will offer no problem to those skilled in the art, and conventional alkaline or acidic materials may be employed.
- the confined, air-tight path comprises a vertical fluid way, particularly an alternately vertically ascending and vertically descending fluid way, such as a series of upright columns through which the mixture of pulp and bleaching material flows in series.
- the pulp-consistency, concentration of hydrosulphite and pglyphosphate, temperature and pH, are as mentioned a ove.
- the pulp suspension may be treated to de-water it, in accordance with the usual practice, or may be made directly into paper.
- the suspension may be diluted and sent to a bull screen where any chunks of wood not previously removed are removed, following which the suspension may be diluted further, for example to about 0.3-0.4% consistency.
- the pulp may be tie-watered on a wet lap machine, for example, to a consistency of about 25%, and then pressed to a consistency of about 50%.
- Example 1 To ground wood pulp, at a temperature of about 175 F. and at a consistency of about 3%, is added an aqueous solution of sodium hydrosulphite and sodium tetraphosphate. The amounts of those materials added are 1% and 0.5%, by weight, respectively, based on the weight of the dry pulp. The solution of sodium hydrosulphite and sodium tetraphosphate is mixed with the pulp with vigorous agitation and the pulp is then held without agitating for about 5 minutes. At the end of this time, the pulp is diluted to 0.3% consistency, and paper is made from the pulp in the usual fashion. The resulting paper has a brightness of 69% (as measured on the General Electric Reflectance Meter) as compared to the unbleached pulp which has a brightness of 58%.
- the method of bleaching mechanically-disintegrated wood pulp which comprises intimately mixing with said pulp at a temperature between about 120 F. and about 212 F., a water-soluble hydrosulphite and a watersoluble polyphosphate, said polyphosphate being mixed with said pulp at a time not substantially later than that at which said hydrosulphite .is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching, and said mixture of pulp, hydrosulphite and polyphosphate having a pH between about 3 and about 8.5.
- the method of bleaching mechanically-disintegrated wood pulp which comprises intimately mixing with said pulp at a temperature between about 120 F. and about 212 F., a water-soluble hydrophosphite and an alkali metal polyphosphate, said alkali-metal polyphosphate being mixed with said pulp at a time not substantially later than that at which said hydrosulphite is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching.
- alkali metal polyphosphate comprises a sodium polyphosphate
- the method of bleaching mechanically-disintegrated wood pulp which comprises mixing with said pulp, at a consistency of between about 0.5% and about 10% and at a temperature between about 120 F. and about 212 F., a water-soluble hydrosulphite and an alkali metal polyphosphate, said polyphosphate being mixed with said pulp at a time not substantially laterthan that at which said hydrosulphite is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching, and said mixture of pulp, hydrosulphite and alkali-metal polyphosphate having a pH between about 3 and about 8.5.
Description
United States Patent fiFice 2,707,144 Patented Apr. 26, 1955 METHOD OF BLEACHING MECHANICALLY DISINTEGRATED WOOD PULP Donald B. Sparrow and James J. Eberl, Moylan, and Kenneth W. Britt, Norwood, Pa., assignors to Scott Paper Company, Chester, Pa., a corporation of Pennsylvania No Drawing. Application August 8, 1951, Serial No. 240,982
14 Claims. (Cl. 8-104) The present invention relates to an improved process for bleaching wood pulp, and more particularly it relates to an improved process for bleaching mechanically-disintegrated wood pulp involving the use of a water-soluble hydrosulphite in conjunction with an agent providing a markedly-improved bleach.
The bleaching of Wood pulp, particularly mechanically-disintegrated wood pulp, is well known. One of the bleaching agents which have been suggested for this purpose is a water-soluble hydrosulphite. By the use of a hydrosulphite, the brightness of mechanically-disintegrated wood pulp, which is normally in the neighborhood of about 60% when measured by the General Electric Reflectance Meter, can be increased a few points at the most. Attempts have been made to increase this bleaching effect through the use of pH control, temperature control, buffering agents, whitening agents, and the like. However, no substantial improvements resulted from these attempts.
It is a principal object of the present invention to pro vide an improved process for bleaching mechanicallydisintegrated wood pulp wherein the brightness increase is markedly greater than that obtained by prior methods.
Another object of the present invention is to provide an improved method for bleaching mechanically-disintegrated wood pulp involving the use of a water-soluble hydrosulphite wherein the brightness increase realized is markedly greater than that obtained through prior methods involving the use of a hydrosulphite.
Still another object of the present invention is to provide a simple method for bleaching mechanicallydisintegrated wood pulp involving the use of a watersoluble hydrosulphite in conjunction with another agent, whereby the brightness increase obtained is substantially greater than that obtained through the use of a watersoluble hydrosulphite alone.
Further objects will be apparent from a consideration of the following specification and claims.
The bleaching process of the present invention comprises intimately mixing, with mechanically-disintegrated wood pulp at an elevated temperature, a water-soluble hydrosulphite and a water-soluble polyphosphate. The polyphosphate will be mixed with the pulp at a time not substantially later than that at which the hydrosulphite is mixed with the pulp, and preferably the hydrosulphite and polyphosphate are mixed substantially simultaneously with the wood pulp. The hydrosulphite and polyphosphate are left in contact with the pulp until the desired bleaching is obtained.
By the use of a water-soluble polyphosphate in conjunction with a water-soluble hydrosulphite in accordance with the present invention, a substantial increase in brightness in the treated wood pulp is obtained, and this increase is substantially greater than the increase obtained when a hydrosulphite alone is employed. While the exact reason for this is not fully understood, the followin theory is advanced by way of explanation. Mechanically-disin- 'tegrated wood pulp contains metal ions including iron, manganese, copper, nickel and cobalt, the iron predominating. Water-soluble hydrosulphites are relatively unstable in solution particularly at elevated temperatures, and this instability appears to be aggravated to a very great extent in the presence of wood pulp. It is, therefore, believed that the stated metal ions catalyze the decomposition of the hydrosulphite. This rapid decomposition of the hydrosulphite prevents that material from exerting its fullest bleaching effect. Since experiments have shown that, in mechanically-disintegrated wood pulp, the hydrosulphite is about five times more stable when a polyphosphate is present, it is believed that the polyphosphate combines with the stated metal ions forming complexes therewith, thus preventing their adverse efiect on the hydrosulphite. This belief is further strengthened by the fact that if the polyphosphate is added to the wood pulp some time after the hydrosulphite is added thereto, the advantages of the present invention are not realized. Thus, as indicated above, the polyphosphate must be incorporated in the wood pulp not substantially later than the time at which the hydrosulphite is mixed with the wood pulp. Regardless of the theory, it is a fact that the incorporation of the polyphosphate with the hydrosulphite in the wood pulp results in a marked improvement in the bleaching etfect realized from the hydrosulphite.
Moreover, mechanically-disintegrated wood pulp contains a relatively high concentration of lignins which often react with certain of the metal ions, particularly iron, to form highly coloring products. The combining of the polyphosphate with the stated metal ions thus also prevents the metal ions from combining with the lignin accounting for a further increase in brightness.
Referring to the Wood pulp treated in accordance with the present invention, it is, as stated, mechanically-disintegrated wood pulp. There are two types of such Wood pulp: (1) ground wood pulp and (2) semichemical wood pulp. Ground wood pulp, as is well-known, is obtained merely by grinding logs to reduce the logs to fibers. Semi-chemical wood pulp is obtained by first reducing the log to chips, treating the chips briefly with chemicals. such as sodium sulphite and sodium bicarbonate, at elevated temperature and pressure preliminarily to soften the chips somewhat, and grinding the chips to fibers. Both ground Wood pulp and semi-chemical wood pulp are relatively high in lignin content, and accordingly, present a particularly ditficult problem, from the standpoint of bleaching, as compared to normal chemical pulp.
The pulp treated in accordance with the present invention may be obtained from several different sources. That is to say it may be ground wood pulp or semi-chemical pulp coming directly from the grinder, or from a point in the pulp-processing procedure remote from the grinder. On the other hand, the pulp coming from the grinder may be first dried and baled, and the bales shipped to a distant point where they are broken up and re-pulped. The pulp treated in accordance with the present invention may be such re-pulped material. The source of the pulp treated in accordance with the present invention is relatively immaterial so long as during the bleaching process it has the proper consistency. Generally, the consistency of the pulp treated in accordance with the present process will be at least about 0.5%, by weight, and the con sistency thereof may range up to the point where satisfactory mixing is not feasible, for example up to 10%, or even 15%, by weight, if desired. Preferably, however, the consistency of pulp is between about 2% and about 5%, by weight. Generally, both the pulp coming directly from the grinder and the re-pulped material will have a consistency Within these ranges. The consistency of pulp obtained from other points in the pulp-processing treatment may require adjustment, and, if such be the case, the consistency of the pulp can be adjusted to the desired level by simply adding or removing water.
As stated previously, the treatment in accordance with the present invention is at an elevated temperature. That is to say, the temperature of the pulp during the treatment :will be above normal room temperature, and generally will be above about F., more generally above about F. While the temperature of the pulp may range as high as 212 F., no advantage is to be gained by operating at such temperatures, and a preferred operating range is between about and about F. The provision of the stated temperatures will ofier no problem to those skilled in the art. In the event fresh ground wood pulp, that is the slurry coming directly from the grinder, is being treagad, such pulp will generally be at a satisfactory temperature due to the heat generated during the grinding operation.
In accordance with the process of the present invention there is added to the stated wood pulp, a water-soluble hydrosulphite as the main bleaching agent. Watersoluble hydrosulphites employed for bleaching wood pulp are well-known and include zinc hydrosulphite, the alkali metal hydrosulphites, such as sodium hydrosulphite and potassium hydrosulphite, ammonium hydrosulphite, and the like. Of the various water-soluble hydrosulphites, sodium hydrosulphite and zinc hydrosulphite, particularly the former, are preferred. The hydrosulphite may be added to the pulp in solid form or as a solution in water. However, in order to insure intimate mixing of the hydrosulphite with the pulp, it is preferred that the hydrosulphite first be dissolved in water and the resulting solution then mixed with the pulp. The amount of hydrosulphite incorporated in the pulp may vary somewhat depending upon the type of pulp treated, the degree of brightness increase desired, and other factors known to those skilled in the bleaching art. Generally, the amount of hydrosulphite mixed with the pulp will be at least about 0.25 by weight, based on the weight of the dry pulp. While amounts of hydrosulphite as high as about 5% or even higher, may be employed, no significant advantage is to be gained by using amounts substantially in excess of about 3%, by weight. Preferably, the amount of hydrosulphite employed will be between about 0.5% and about 1.5%, by weight, based on the dry weight of the pulp.
Referring again to the polyphosphate employed in accordance with the present process, it will, as stated, be any of the water-soluble polyphosphates, that is, a polyphosphate having the formula (M2O)P2O5 wherein M is a monovalent cation providing water-solubility to the compound and wherein x is less than 3. Examples of monovalent cations providing water-solubility to the compound are hydrogen, NH4, the alkali metals, such as sodium and potassium, and the like. Mixtures of polyphosphates may be employed if desired. The polyphosphate employed may be of the crystalline type or of the glassy type. Examples of polyphosphates that may be employed in accordance with the present invention (using sodium for M for the purpose of illustration) are sodium pyrophosphate (Na4P2O7) wherein x is 2, sodium tetraphosphate (NaePrOm) wherein x is 1.5, sodium tripolyphosphate (NaaPsOro) wherein x is 1.67, sodium hexapolyphosphate (NasPsOrs) wherein x is 1.33, sodium heptapolyphosphate (Na9P'zO22) wherein x is 1.29, sodium decapolyphosphate (NamPmOar) wherein x is 1.2, and the like. Of the polyphosphates mentioned, those in which x in the above formula is between about 1 and about 2, and particularly where M is an alkali metal, especially sodium, are preferred. As specific preferred polyphosphates, sodium tetraphosphate and sodium pyrophosphate, especially the former, may be mentioned.
As in the case with the hydrosulphite, the polyphosphate may be added to the wood pulp as a solid or as an aqueous solution thereof, preferably the latter. The amount of polyphosphate employed may vary somewhat depending upon the type of pulp treated and the degree of brightness increase desired. In most cases the amount of polyphosphate employed will be at least about 0.1%, by weight, based on the weight of the dry pulp. While amounts of polyphosphate as high as about 5% or even higher, may be employed, no significant advantage is to be gained by the use of amounts of polyphosphate substantially in excess of about 23%. Preferably, the amount of polyphosphate employed is between about 0.3% and about 1%, by weight, based on the weight of the dry pulp.
As stated previously, the polyphosphate will be added to the pulp not substantially later than the time when the hydrosulphite is added to the pulp. This means, of course, that the polyphosphate may be added to the pulp at any time before, or at the same time as the hydrosulphite is added thereto, or may even be added directly after the hydrosulphite is added to the pulp. Thus, the term not substantially later when used in connection with the time of addition of the polyphosphate to the pulp in relation to the time of addition of the hydrosulphite, means that any delay between the addition of the hydrosulphite to the pulp and the addition of the polyphosphate to the pulp will not be such as will permit a substantial amount of the hydrosulphite to be decomposed before the polyphosphate is mixed therewith. As stated previously, the polyphosphate and the hydrosulphite are preferably mixed substantially simultaneously with the wood pulp. Thus, the hydrosulphite and the polyphosphate may be added separately but substantially simultaneously, or the hydrosulphite and the polyphosphate may be premixed, for example, in water, and the resulting mixture added to the pulp. This latter means is the preferred Way of incorporating and mixing the hydrosulphite and polyphosphate with the wood pulp.
The hydrosulphite and polyphosphate, as stated, must be intimately mixed with the wood pulp. This intimate mixture may be obtained through a wide variety of means, such as the use of conventional mixing blades, and the like. Following mixing, the hydrosulphite and polyphosphate are permitted to remain in contact with the pulp until the desired bleaching has taken place. This time of contact may be varied depending upon the amounts of hydrosulphite and of polyphosphate employed, the temperature conditions employed, the type of pulp treated, the degree of brightness desired, as well as the other considerations known to those skilled in the bleaching art. However, in general, the time may range from as little as a few minutes, for example three minutes, up to an hour and a half or even longer. Under the preferred operating conditions referred to above, satisfactory bleaching may be obtained in from about 10 to about 30 minutes.
The pH of the mixture during the process should not be permitted to become substantially alkaline, that is to say, the pH of the medium during the bleaching treatment should not be substantially in excess of about 8.5. A pH on the acid side of neutrality may be, and preferably is, employed, and a pH as low as about 3 is satisfactory. The precise pH employed will depend somewhat upon the nature of the hydrosulphite and polyphosphate selected, for example, when the polyphosphate is an alkali metal salt, the pH may be somewhat higher than when the cation is one of the other mentioned materials. In most cases, the pH will range between about 4 and about 6.5, with pI-Is between about 5 and about 6 being preferred. The adjustment of the pH, if after the addition of the hydrosulphite and polyphosphate such adjustment is desired, will offer no problem to those skilled in the art, and conventional alkaline or acidic materials may be employed.
An advantageous method of mixing the hydrosulphite and polyphosphate with the wood pulp, and carrying out the bleaching treatment in general, is the process described and claimed in co-pending application Serial No. 240,897, filed August 8, 1951. In accordance with that process, the bleaching material, in aqueous solution, is continuously fed to a continuously-moving stream of the wood pulp. Thereafter, the mixture of bleaching material and pulp is subjected to combined vigorous agitation whereby the solution of bleaching material is intimately mixed with the pulp, and propulsion forcing the mixture of pulp and bleaching material as a continuously-moving stream, preferably characterized by streamlined plug flow, along a confined, air-tight path. The flowing mixture of pulp and bleaching material will substantially fill the cross-section of the confined path. The mixture is flowed continuously in the closed circuit until the desired bleaching is obtained. In accordance with the preferred embodiment of that process, the confined, air-tight path comprises a vertical fluid way, particularly an alternately vertically ascending and vertically descending fluid way, such as a series of upright columns through which the mixture of pulp and bleaching material flows in series. The pulp-consistency, concentration of hydrosulphite and pglyphosphate, temperature and pH, are as mentioned a ove.
After the desired bleaching has been obtained, the pulp suspension may be treated to de-water it, in accordance with the usual practice, or may be made directly into paper. For example, the suspension may be diluted and sent to a bull screen where any chunks of wood not previously removed are removed, following which the suspension may be diluted further, for example to about 0.3-0.4% consistency. After the diluted, bleached pulp is run through a fine screen, if desired, the pulp may be tie-watered on a wet lap machine, for example, to a consistency of about 25%, and then pressed to a consistency of about 50%.
While the foregoing description has dealt primarily with a hydrosulphite as the bleaching agent, it will be realized that the process is not limited to a hydrosulphite as the sole bleaching agent and that other bleaching agents may be employed in conjunction with the hydrosulphite.
Likewise, the process is not limited to the use of a polyphosphate as the sole supplemental agent and it will be understood that other agents may be included for what ever effect desired.
The process of the present invention will be more readily understood from a consideration of the following specific example which is given for the purpose of illustration only and is not intended to limit the scope of the invention in any way.
Example To ground wood pulp, at a temperature of about 175 F. and at a consistency of about 3%, is added an aqueous solution of sodium hydrosulphite and sodium tetraphosphate. The amounts of those materials added are 1% and 0.5%, by weight, respectively, based on the weight of the dry pulp. The solution of sodium hydrosulphite and sodium tetraphosphate is mixed with the pulp with vigorous agitation and the pulp is then held without agitating for about 5 minutes. At the end of this time, the pulp is diluted to 0.3% consistency, and paper is made from the pulp in the usual fashion. The resulting paper has a brightness of 69% (as measured on the General Electric Reflectance Meter) as compared to the unbleached pulp which has a brightness of 58%.
The same ground wood pulp treated similarly but without the addition of any polyphosphate, resulted in a paper having a brightness only 4 points greater than that of the unbleached pulp.
In another example, a pulp having an initial brightness of 61% and which could be brightened 7.7 points by the use of the hydrosulphite alone, had its brightness increased to 72% by the use of sodium tetraphosphate in conjunction with the hydrosulphite, following the procedure of the above example.
Considerable modification is possible in the selection of the various ingredients as well as in the particular technique followed in carrying out the process without departing from the scope of the invention.
We claim:
1. In the bleaching of mechanically-disintegrated wood pulp by the use of a water-soluble hydrosulphite, the improvement which comprises mixing with said wood pulp, at a time not substantially later than that at which the hydrosulphite is mixed with the pulp, a water-soluble polyphosphate, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching.
2. The method of claim 1 wherein the temperature of the pulp is between about 120 F. and about 212 F.
3. In the bleaching of mechanically-disintegrated wood pulp wherein a water-soluble hydrosulphite is mixed with the pulp, the improvement which comprises mixing with the wood pulp, substantially simultaneously with the hydrosulphite, a water-soluble polyphosphate.
4. The method of claim 3 wherein the temperature of the2 wg od pulp is between about 120 F. and about 21 5. The method of bleaching mechanically-disintegrated wood pulp which comprises intimately mixing with said pulp at a temperature between about 120 F. and about 212 F., a water-soluble hydrosulphite and a watersoluble polyphosphate, said polyphosphate being mixed with said pulp at a time not substantially later than that at which said hydrosulphite .is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching, and said mixture of pulp, hydrosulphite and polyphosphate having a pH between about 3 and about 8.5.
6. The method of claim 5 wherein the pH of the mixture is between about 4 and about 6.5.
7. The method of bleaching mechanically-disintegrated wood pulp which comprises intimately mixing with said pulp at a temperature between about 120 F. and about 212 F., a water-soluble hydrophosphite and an alkali metal polyphosphate, said alkali-metal polyphosphate being mixed with said pulp at a time not substantially later than that at which said hydrosulphite is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching.
8. The method of claim 7 wherein said alkali metal polyphosphate comprises a sodium polyphosphate.
9. The method of bleaching mechanically-disintegrated wood pulp which comprises mixing with said pulp, at a consistency of between about 0.5% and about 10% and at a temperature between about 120 F. and about 212 F., a water-soluble hydrosulphite and an alkali metal polyphosphate, said polyphosphate being mixed with said pulp at a time not substantially laterthan that at which said hydrosulphite is mixed with said pulp, whereby the hydrosulphite and polyphosphate are in admixture with said wood pulp during bleaching, and said mixture of pulp, hydrosulphite and alkali-metal polyphosphate having a pH between about 3 and about 8.5.
10. The method of claim 9 wherein the consistency of said pulp is between about 2% and about 5%; wherein the temperature of said pulp is above about 135 F.; wherein said alkali-metal polyphosphate comprises a sodium polyphosphate; wherein said polyphosphate is mixed with said pulp substantially simultaneously with said hydrosulphite, and wherein the pH of the mixture of pulp, hydrosulphite and alkali-metal polyphosphate is between about 4 and about 6.5.
11. The method of claim 10 wherein the temperature of said pulp is between about 160 and about 190 F.; wherein said sodium polyphosphate is one in which the mol ratio of NazO to P205 is between about 1:1 and about 2: 1, and wherein the pH of said mixture is between about 5 and about 6.
12. The method of claim 11 wherein said water-soluble hydrosulphite is sodium hydrosulphite and wherein said sodium polyphosphate is sodium tetraphosphate.
13. The method of claim 10 wherein the amount of hydrosulphite employed is between about 0.25 and about 5%, by weight, based on the weight of the dry pulp, and wherein the amount of sodium polyphosphate employed is between about 0.1 and about 5%, by weight, based on the weight of the dry pulp.
14. The method of claim 10 wherein the amount of hydrosulphite employed is between about .5 and about 1.5%, by weight, based on the weight of the dry pulp, and wherein the amount of sodium polyphosphate employed is between about 0.3 and about 1%, by weight, based on the weight of the dry pulp.
References Cited in the file of this patent UNITED STATES PATENTS 1,333,029 MacIntyre Mar. 9, 1920 2,071,304 Hirschkind Feb. 16, 1937 2,071,307 Hirschkind Feb. 16, 1937 2,072,665 Campbell Mar. 2, 1937 2,073,923 Crocker Mar. 16, 1937 2,121,397 Downing June 21, 1938 2,130,321 Kharasch Sept. 13, 1938 FOREIGN PATENTS 13,753 Great Britain 1913 811,938 France Apr. 26, 1937 OTHER REFERENCES Lang et al.: Metaphosphate Increases the Washing Efliciency of Chemical Pulps, Paper Trade Jour., vol. 116, No. 20, pp. 33 to 36 (Tappi Sec., pp. 227 to 230), May 20, 1943.
Rittenhouse: Groundwood Bleaching with Zinc Hydrosulphite," Paper Trade Jour., vol. 131, No. 18, pp. 30, 36, November 2, 1950.
Reichert: Sodium Peroxide Bleaching of Mechanical Pulps-Control of Metal Catalysts in the Bleaching Operation, Paper Trade Jour., vol. 118, No. 15, April 13, 1944, pp. 45 to 48.
Claims (1)
1. IN THE BLEACHING OF MECHANICALLY-DISINTEGRATED WOOD PULP BY THE USE OF A WATER-SOLUBLE HYDROSULPHITE, THE IMPROVEMENT WHICH COMPRISES MIXING WITH SAID WOOD PULP, AT A TIME NOT SUBSTANTIALLY LATER THAN THAT AT WHICH THE HYDROSULPHITE IS MIXED WITH THE PULP, A WATER-SOLUBLE POLYPHOSPHATE, WHEREBY THE HYDROSULPHITE AND POLYPHOSPHATE ARE IN ADMIXING WITH SAID WOOD PULP DURING BLEACHING.
Priority Applications (2)
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US240982A US2707144A (en) | 1951-08-08 | 1951-08-08 | Method of bleaching mechanically disintegrated wood pulp |
DES42472A DE1052797B (en) | 1951-08-08 | 1955-01-28 | Process for bleaching wood pulp |
Applications Claiming Priority (1)
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US240982A US2707144A (en) | 1951-08-08 | 1951-08-08 | Method of bleaching mechanically disintegrated wood pulp |
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US2707144A true US2707144A (en) | 1955-04-26 |
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US240982A Expired - Lifetime US2707144A (en) | 1951-08-08 | 1951-08-08 | Method of bleaching mechanically disintegrated wood pulp |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US2826478A (en) * | 1955-07-19 | 1958-03-11 | Rohm & Haas | Method of bleaching mechanically-disintegrated wood pulp with hydrosulfite bleach containing an alkali metal citrate |
US2862784A (en) * | 1955-03-04 | 1958-12-02 | Virginia Smelting Company | Oxidative-reductive multi-stage bleaching of ground wood pulp |
US2963395A (en) * | 1958-03-31 | 1960-12-06 | Crown Zellerbach Corp | Process of bleaching lignocellulosic pulps |
US3016324A (en) * | 1957-03-07 | 1962-01-09 | Bauer Bros Co | Method and apparatus for producing wood pulp |
US3023140A (en) * | 1958-11-24 | 1962-02-27 | Bauer Bros Co | Pulp bleaching |
US3055792A (en) * | 1958-08-12 | 1962-09-25 | West Virginia Pulp & Paper Co | Bleaching cold caustic pump with so2 |
US3262883A (en) * | 1962-11-13 | 1966-07-26 | Rohm & Haas | Defouling ion exchange resins by the removal of iron oxides therefrom |
US3653804A (en) * | 1966-12-31 | 1972-04-04 | Basf Ag | Bleaching of wood pulp with dithionite solution stabilized by zinc compound |
US3985674A (en) * | 1974-12-10 | 1976-10-12 | Virginia Chemicals Inc. | Stabilized sodium dithionite solutions |
US20040117914A1 (en) * | 2002-11-05 | 2004-06-24 | Sibiet Jean Luc | Method for brightening virgin mechanical pulp |
CN102926186A (en) * | 2012-10-12 | 2013-02-13 | 濮阳宏业汇龙化工有限公司 | Powerful reduced powder |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US2862784A (en) * | 1955-03-04 | 1958-12-02 | Virginia Smelting Company | Oxidative-reductive multi-stage bleaching of ground wood pulp |
US2826478A (en) * | 1955-07-19 | 1958-03-11 | Rohm & Haas | Method of bleaching mechanically-disintegrated wood pulp with hydrosulfite bleach containing an alkali metal citrate |
US3016324A (en) * | 1957-03-07 | 1962-01-09 | Bauer Bros Co | Method and apparatus for producing wood pulp |
US2963395A (en) * | 1958-03-31 | 1960-12-06 | Crown Zellerbach Corp | Process of bleaching lignocellulosic pulps |
US3055792A (en) * | 1958-08-12 | 1962-09-25 | West Virginia Pulp & Paper Co | Bleaching cold caustic pump with so2 |
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US3653804A (en) * | 1966-12-31 | 1972-04-04 | Basf Ag | Bleaching of wood pulp with dithionite solution stabilized by zinc compound |
US3985674A (en) * | 1974-12-10 | 1976-10-12 | Virginia Chemicals Inc. | Stabilized sodium dithionite solutions |
US20040117914A1 (en) * | 2002-11-05 | 2004-06-24 | Sibiet Jean Luc | Method for brightening virgin mechanical pulp |
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CN102926186A (en) * | 2012-10-12 | 2013-02-13 | 濮阳宏业汇龙化工有限公司 | Powerful reduced powder |
CN102926186B (en) * | 2012-10-12 | 2014-05-14 | 濮阳宏业汇龙化工有限公司 | Powerful reduced powder |
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