US1795757A - Method of bleaching and process for preparing liquors therefor - Google Patents
Method of bleaching and process for preparing liquors therefor Download PDFInfo
- Publication number
- US1795757A US1795757A US261698A US26169828A US1795757A US 1795757 A US1795757 A US 1795757A US 261698 A US261698 A US 261698A US 26169828 A US26169828 A US 26169828A US 1795757 A US1795757 A US 1795757A
- Authority
- US
- United States
- Prior art keywords
- bleaching
- pulp
- permanganate
- hypochlorite
- manganate
- 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.)
- Expired - Lifetime
Links
- 238000004061 bleaching Methods 0.000 title description 52
- 238000000034 method Methods 0.000 title description 33
- 238000004519 manufacturing process Methods 0.000 title description 12
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 42
- 239000000463 material Substances 0.000 description 32
- 239000000243 solution Substances 0.000 description 27
- 239000007844 bleaching agent Substances 0.000 description 21
- LBSANEJBGMCTBH-UHFFFAOYSA-N manganate Chemical compound [O-][Mn]([O-])(=O)=O LBSANEJBGMCTBH-UHFFFAOYSA-N 0.000 description 21
- 239000002131 composite material Substances 0.000 description 19
- 230000008569 process Effects 0.000 description 18
- 239000000460 chlorine Substances 0.000 description 15
- 229910052801 chlorine Inorganic materials 0.000 description 15
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 13
- 239000002657 fibrous material Substances 0.000 description 12
- 239000003513 alkali Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000002023 wood Substances 0.000 description 8
- 229920001131 Pulp (paper) Polymers 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000001340 alkali metals Chemical class 0.000 description 5
- 238000010411 cooking Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- JYLNVJYYQQXNEK-UHFFFAOYSA-N 3-amino-2-(4-chlorophenyl)-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(CN)C1=CC=C(Cl)C=C1 JYLNVJYYQQXNEK-UHFFFAOYSA-N 0.000 description 4
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 4
- -1 bleaching powder Chemical class 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 239000005708 Sodium hypochlorite Substances 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- BNBLBRISEAQIHU-UHFFFAOYSA-N disodium dioxido(dioxo)manganese Chemical compound [Na+].[Na+].[O-][Mn]([O-])(=O)=O BNBLBRISEAQIHU-UHFFFAOYSA-N 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000556720 Manga Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 2
- 150000008041 alkali metal carbonates Chemical class 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000007500 overflow downdraw method Methods 0.000 description 2
- SIWNEELMSUHJGO-UHFFFAOYSA-N 2-(4-bromophenyl)-4,5,6,7-tetrahydro-[1,3]oxazolo[4,5-c]pyridine Chemical compound C1=CC(Br)=CC=C1C(O1)=NC2=C1CCNC2 SIWNEELMSUHJGO-UHFFFAOYSA-N 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910000616 Ferromanganese Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 244000273256 Phragmites communis Species 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000002761 deinking Substances 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/1078—Bleaching ; Apparatus therefor with Mn-containing compounds
Definitions
- the bleaching treatment tends to injure or weaken the fibres.
- bearing compounds sometimes has a natural wood tint, rendering it inferior for the better qualities of product, and its ash content may be increased by the bleaching operation, particularly when bleaching powder lsused.
- manganates as well as permanganates can be successfully and advantageously employed in the bleaching process of the present invention, as for example, in conjunction with chlorine or/and hypochlorite.
- the manganates are usually less eflicient than the permanganates; and we I regard the use of permanganates as more advantageo us than the use of manganates for bleaching fibrous material, e. g., pulp.
- Permanganates can be produced from manganates by oxidation-with suitable agents; and this production of perma-nganates and their subsequent use according to the present invention can advantageously be combined.
- sodium manganate admixed with an excess of alkali (such as sodium hydroxide), may be treated with chlorine to oxidize the sodium manganate to sodium permanganate and to form typochlorite with the excess alkali; and the resulting mixture can then be utilized as a composite bleaching or oxidizing agent, as hereinafter more fully described.
- alkali such as sodium hydroxide
- the permanganates which we consider particularly advantageous are sodium'permanganate and alkaline earth metal permanganate, such as calcium permanganate.
- Potassium permanganate hasa limited solubility, as compared with sodium permanga- Application filed. March 14, 1928. Serial No. 261,698.
- the permanganates canbe used in either acid, neutral or alkaline solution, and with temperature within a limited degree, by more intense agitation, etc., and this is desirable for the purpose of control in bleaching certain materials, particularly where acid is not present for example, the material may be heated up to 30 deg. (l, or to any suitable temperature, up toboiling, but it is one advantage of the process that it can be carried out expeditiously with but moderate heating, thus reducing the liability of injuring the fibrous materials so treated.
- the bleaching liquor can advantageously be prepared in the form of a strong stock solution and added in predetermined amounts to thefibrous material to be bleached.
- the fibres may be mixed with and distributed containing manganate or permanganate to the material to be bleached, we find it advantageous to gradually introduce the solution,
- the strong solution may be sprinkled or sprayed or atomized into the mixture.
- the material can then be directly treated with sulfur dioxide or solution of sulfurous'acid, a bi-sulfite, or a sulfite and acid; or it can with advantage be separated from its accompanying liquor to a. greater 01' less extent before the sulfurous treatment, for example, by washing the material so that a fair portion of the original.
- the amount of sulfur .dioxide or other sulfurous material required for removing from the fibrous material, the brown material (if any) produced by action of a manganate or permanganate, may vary somewhat with,
- colorless or white manganese salts may be left with the wet pulp. They may then combine with the alkaline size if any is used. However, such salts may be removed from such pulp, and, if the pulpis to be dried, care-should be taken to remove objectionable compounds by washing the bleached pulp after the bleaching operation.
- the bleaching agents when alkali metalcompounds are used, are readily soluble so that the bleached and washed fibrous mate.- rial is relatively low in ash as well of good white color and excellent texture.
- the bleaching process moreover, is one which can be carried out at a moderate or relatively low temperature.
- the permanganate which may be used in the present invention may advantageously be produced from manganate.
- Alkali metal manganates are commonly made by fusion methods which leave an excess of alkali, such as sodium oxide or hydroxide, with the manganate, when good yields are obtained. Instead of neutralizing this excess of alkali with an acid, we have found that it is advantageous to leave it with the manganate, and then treat the mixture of manganate and excess alkali in solution, or in suspension in part, with chlorine, either after or before adding the mixture to the fibrous material to be bleached.
- Chlorine ganate will act upon the manganate to form permanganate and it will also act upon the excess alkali to form hypochlorite, so that if enough chlorine be added there will be produced a composite solution containing both permanganate and hypochlorite.
- such a composite bleaching solution is admixed with the pulp or other material to be bleached, or when the composite bleaching solution is produced. in admixture with. the pulp or other material (as hereinafter described), the hypochlorite, especially when present in relatively-large amount in alkaline solution, appears toact through the perman- Ferhaps by reoxidizing any manganate (i any) formed by reduction of permanganate in presence of organic matter and reconverting it into permanganate, although we do not desire to limit our by any suchiexplanation if other chemical action takes place when such a composite bleach liquor is used.
- hypochlorite in such composite bleach liquor, appears to act in a different and more advantageous manner than when used alone, while the action of the permanganate is supplemented by the action of the hypochlorite so that a lesser amount of permanganate need be used than if the permanganate alone were relied upon.
- this composite bleaching agent containing sodium permanganate and sodium hypochlorite and its use are new in the art; and we claim such composite bleaching agent as our invention or discovery, as well as the method of bleaching in which such composite agent is employed, and also the method of preparing such composite agent. Owing to its characteristic composition-and properties, this composite agent can alsobe adva ntageously used for other purposes than bleaching, e. g., as a disinfectant, deodorant, germicide, for water purification, sewage treatment, cleaning purposes, etc.
- the composite bleaching agent may be directly made in solution at the time and place of use.
- sodium manganate is made by a fusion method and contains an excess of soda
- this material can be shipped in a solid state to a laundry, textile factory, pulp mill, paper mill, etc., and there dissolved in water, and the solution treated with gaseous chlorine suflicient to oxidize the manganate to permanganate and produce hypochlorite by reaction upon excess soda.
- This resulting solution can then be added directly to the pulp or other material to be bleached.
- the manganate or permanganate contains less than a desired amount of excess alkali
- suitable alkali or alkaline compounds can be added before the treatment with chlorine, and the composite solution will be obtained.
- the manganateor permanganate and excess alkali or other suitable compound can be added to and mixed with'the' pulp or other material to be bleached and the chlorine about 3 parts of sodium permanganate, or
- sodium hypochlorite (or its equivalent as stated).
- Such amounts of such bleaching reagents may be employed on about 100 parts (air-dry weight) of the pulp such as chemical pulp derived from Wood. Suitable ratios of such reagents intermediate to such proportions may be used, in each case employing such an amount of bleaching material. as is required to effect the desired degree of bleach ing, although a moderate excess over such needed amount may be used. This-may facilitate the bleaching treatment.
- the proportions of permanganate and hypochlorite in the composite bleach solution can be varied and regulated, for example, by varying and regulating the amount of free alkali in" admixture with the ma-nganate which is to be treated with chlorine.
- a composite bleach solution of regulated permanganate and hypochlorite content can be made by dissolving known amounts of separately produced permanganate and hypochlorite. Such solutions can be produced prior to the addition of the composite bleaching solution to the pulp or other material to be bleached, or
- the mixture may be produced, for example,
- the pulp or other material to be washing the pulp or other material to be bleached, after the manggiiate orpermanganate and hypochlorite treatment, the pulp, etc. can be freed from the greater part of the compounds in solution, prior to the sulfur dioxide or other treatment for dissolving a manganese compound.
- sulfur dioxide for converting a compound'of manganese into a soluble form
- other agents. which convert such compound into colorless and soluble compounds can be similarly used.
- Acid alone can be used for this purpose, such as hydrochloric acid or sulfuric acid, but a considerable amount of such acid will-be re quired unless the action is carried out or finished at an elevated temperature, or allowed to stand for considerable time, and the fibres may be injured thereby.
- the treatment With sulfur dioxide or sulfurous acid has the advantage that it takes place readily and quickly at ordinary temperature.
- WVhile we have described the invention more particularly in connection with the bleaching ofpulp, e. g., pulp derived-from wood, for which it is particularly advan tageous, yet it will be understood that the invention is also applicable to the bleaching of other fibrous materials, such as cotton, silk, linen, wool, etc., in a similar manner, as well as paper pulp stocks recovered through deinking processes, etc., and we include the bleaching of such materials within the more comprehensive claims appended hereto.
- the advantages of the process of the present invention is the uniformity of the bleaching action and the desirable condition in which the fibres are left.
- the fibres, for example, of cotton, silk, pulp, etc. are thus in a form well adapted for subsequenttreatment, e. g., for uniform dyeing, etc.
- the process of the present invention is also of particular value for the bleaching of chemical pulps from wood which are relatively difiicult to bleach by common bleaching methods and enables a superior bleached pulp to be obtained therefrom, of. good white color.
- the process of the present invention is of moreor less general application to the bleaching of fibrous mate rial and. fabrics, etc., of a bleachable character and will give whiter bleached materials and with less injury than with any of the common bleaching methods of which we are aware.
- chlorine or a hypochlorite may be used to bring about a partial bleaching of the material, and the bleaching operation can then be completed with the manganate or permanganate, and, to the extent that residual chlorine or an active chlorine bearing compound remains when the manganate or permanganate is added, the further bleaching operation may be of a character similar to that when a composite bleach liquor containing permanganate and hypochlorite is added. So also, other bleaching agents may be used in conjunction with the manganate or perman anate, to modify the bleaching operation. Terborates or peroxides, for example, may thus be used.
- the invention is not limited thereto, but other suitable manganates and permanganates can be used which are capable of exerting a bleaching or oxidizing action, and such manga'nates or permanganates can be used in conjunction with other agents, e. g., hypochlorites, etc., as hereinbefore described.
- alkali metal manganates or permanganates are employed, they canbe produced by any suitable method of production, such as by fusion, electrolytically, etc.
- One advantageous method of production is by electrolyzing a solution of causticalkali or alkali metal carbonate, using anodes of ferromanganese or other suitable manganesebearing material.
- a manganate to include both manganates and permanganates.
- alkali-forming metal is intended to in-- clude both alkaline earth metals such as calcium, barium or magnesium and alkali metals such as sodium or potassium.
- the process of treating cellulosic-fibrous material to obtain a product relatively high in alpha cellulose comprises subjecting wood pulp obtained from wood by a of chemical pulp from Wood, which comprises preparing a mixture containing such fibres and water, distributing throughout such mixture a solution containing an alkali metal. hypochlorite and a permanganate, treating the fibres by means of bleaching ma.- terials supplied by the solution until substantially all the colored. non-fibrous organic constituents of the pulp have been rendered substantially colorless or readily separable from the fibres, and subsequently treating the resulting fibrous material by means of an acid liquor so as to render soluble a colored tures.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
Description
Patented Mar.- 10, 1931 UNITED STATES PATENT OFFICE LINN IBRADLEY, OE MONTOLAIR, NEW JERSEY, AND EDWARD P. MCKEEFE, OF PLAT'IS- BURG, NEW YORK, ASSIGNORS T0 BRADLEY-MCKEEFE CORPORATION, OF NEW YORK,
N. Y., A. CORPORATION OF NEW YORK METHOD OF BLEACHING AND PROCESS FOR PREPARING LIQUORS THEREFOR No Drawing.
tured into Patent No. 1,768,819, Serial No.
544,322, filed March 16, 1922, which has ma t-ured into .Patent No. 1,768,820 and Serial Nos. 481,146 and 481,147, filed June 28, 1921.
In the common methods of bleaching pulp with chlorine or chlorine-bearing compounds such as bleaching powder, the bleaching treatment tends to injure or weaken the fibres.
So also, wood pulp bleached with chlorine-.
bearing compounds sometimes has a natural wood tint, rendering it inferior for the better qualities of product, and its ash content may be increased by the bleaching operation, particularly when bleaching powder lsused.
We have found that manganates as well as permanganates can be successfully and advantageously employed in the bleaching process of the present invention, as for example, in conjunction with chlorine or/and hypochlorite. The manganates are usually less eflicient than the permanganates; and we I regard the use of permanganates as more advantageo us than the use of manganates for bleaching fibrous material, e. g., pulp. Permanganates can be produced from manganates by oxidation-with suitable agents; and this production of perma-nganates and their subsequent use according to the present invention can advantageously be combined.
For example, sodium manganate, admixed with an excess of alkali (such as sodium hydroxide), may be treated with chlorine to oxidize the sodium manganate to sodium permanganate and to form typochlorite with the excess alkali; and the resulting mixture can then be utilized as a composite bleaching or oxidizing agent, as hereinafter more fully described.
The permanganates which we consider particularly advantageous are sodium'permanganate and alkaline earth metal permanganate, such as calcium permanganate.
Potassium permanganate hasa limited solubility, as compared with sodium permanga- Application filed. March 14, 1928. Serial No. 261,698.
nate, and we have found that its solution is more stable, so that in many instances it is less advantageous for use as a bleaching agent. With sodium permanganate, to explain, stronger solutions can readily be pre pared and only a relatively small or moderate amount of the solution need be added to thematerial to be bleached to obtain the desired bleaching effect.
The permanganates canbe used in either acid, neutral or alkaline solution, and with temperature within a limited degree, by more intense agitation, etc., and this is desirable for the purpose of control in bleaching certain materials, particularly where acid is not present for example, the material may be heated up to 30 deg. (l, or to any suitable temperature, up toboiling, but it is one advantage of the process that it can be carried out expeditiously with but moderate heating, thus reducing the liability of injuring the fibrous materials so treated.
The bleaching liquor can advantageously be prepared in the form of a strong stock solution and added in predetermined amounts to thefibrous material to be bleached. The fibres may be mixed with and distributed containing manganate or permanganate to the material to be bleached, we find it advantageous to gradually introduce the solution,
into a mixture of fibrous-material and water while the latter is being circulated or agitated, thus avoiding the presence of a large excess of the bleach liquor in contact with any one portion of the material to be bleached and minimizing the possibility of the local production of oxycellulose. For example, the strong solution may be sprinkled or sprayed or atomized into the mixture.
After the manganate or permanganate has acted upon the material, the material can then be directly treated with sulfur dioxide or solution of sulfurous'acid, a bi-sulfite, or a sulfite and acid; or it can with advantage be separated from its accompanying liquor to a. greater 01' less extent before the sulfurous treatment, for example, by washing the material so that a fair portion of the original.
liquor is replaced by water, and then treating the fibrous material with sulfurous material after such washing operation.
The amount of sulfur .dioxide or other sulfurous material required for removing from the fibrous material, the brown material (if any) produced by action of a manganate or permanganate, may vary somewhat with,
manganate or permanganate respectively,
and when used for bleaching give up oxygen more readily, and we have found that these manganates and permanganates, nevertheless,;can readily bleach without unduly injuring the fibrous material.
When bleaching pulp which is to remain in the wet form until used in the manufacture of paper, colorless or white manganese salts may be left with the wet pulp. They may then combine with the alkaline size if any is used. However, such salts may be removed from such pulp, and, if the pulpis to be dried, care-should be taken to remove objectionable compounds by washing the bleached pulp after the bleaching operation.
It is one advantage of the present invention that the bleaching agents, when alkali metalcompounds are used, are readily soluble so that the bleached and washed fibrous mate.- rial is relatively low in ash as well of good white color and excellent texture. The bleaching process, moreover, is one which can be carried out at a moderate or relatively low temperature.
As above stated, the permanganate which may be used in the present invention, may advantageously be produced from manganate. Alkali metal manganates are commonly made by fusion methods which leave an excess of alkali, such as sodium oxide or hydroxide, with the manganate, when good yields are obtained. Instead of neutralizing this excess of alkali with an acid, we have found that it is advantageous to leave it with the manganate, and then treat the mixture of manganate and excess alkali in solution, or in suspension in part, with chlorine, either after or before adding the mixture to the fibrous material to be bleached. Chlorine ganate will act upon the manganate to form permanganate and it will also act upon the excess alkali to form hypochlorite, so that if enough chlorine be added there will be produced a composite solution containing both permanganate and hypochlorite.
lVhen such a composite bleaching solution is admixed with the pulp or other material to be bleached, or when the composite bleaching solution is produced. in admixture with. the pulp or other material (as hereinafter described), the hypochlorite, especially when present in relatively-large amount in alkaline solution, appears toact through the perman- Ferhaps by reoxidizing any manganate (i any) formed by reduction of permanganate in presence of organic matter and reconverting it into permanganate, although we do not desire to limit ourselves by any suchiexplanation if other chemical action takes place when such a composite bleach liquor is used. The hypochlorite, in such composite bleach liquor, appears to act in a different and more advantageous manner than when used alone, while the action of the permanganate is supplemented by the action of the hypochlorite so that a lesser amount of permanganate need be used than if the permanganate alone were relied upon.
In so far as we have been able to ascertain, such a composite bleaching agent containing sodium permanganate and sodium hypochlorite and its use are new in the art; and we claim such composite bleaching agent as our invention or discovery, as well as the method of bleaching in which such composite agent is employed, and also the method of preparing such composite agent. Owing to its characteristic composition-and properties, this composite agent can alsobe adva ntageously used for other purposes than bleaching, e. g., as a disinfectant, deodorant, germicide, for water purification, sewage treatment, cleaning purposes, etc.
The composite bleaching agent may be directly made in solution at the time and place of use. For example, if sodium manganate is made by a fusion method and contains an excess of soda, this material can be shipped in a solid state to a laundry, textile factory, pulp mill, paper mill, etc., and there dissolved in water, and the solution treated with gaseous chlorine suflicient to oxidize the manganate to permanganate and produce hypochlorite by reaction upon excess soda. This resulting solution can then be added directly to the pulp or other material to be bleached.
preferably after clarification, if needed. If
the manganate or permanganate contains less than a desired amount of excess alkali, suitable alkali or alkaline compounds can be added before the treatment with chlorine, and the composite solution will be obtained. Instead of producing the composite solution containing permanganate and hypochlorite and subsequentlyadding this solution to the pulp or other material to be bleached, the manganateor permanganate and excess alkali or other suitable compound can be added to and mixed with'the' pulp or other material to be bleached and the chlorine about 3 parts of sodium permanganate, or
its chemical equivalent, to about 1 part more or less of. such permanganate, and from about part. of sodium hypochlorite, or its chemical equivalent in other suitable hypochlorite such as calcium hypochlorite, to
' about 15 parts to 20 parts, more or less, of
sodium hypochlorite (or its equivalent as stated). Such amounts of such bleaching reagents may be employed on about 100 parts (air-dry weight) of the pulp such as chemical pulp derived from Wood. Suitable ratios of such reagents intermediate to such proportions may be used, in each case employing such an amount of bleaching material. as is required to effect the desired degree of bleach ing, although a moderate excess over such needed amount may be used. This-may facilitate the bleaching treatment. The proportions of permanganate and hypochlorite in the composite bleach solution can be varied and regulated, for example, by varying and regulating the amount of free alkali in" admixture with the ma-nganate which is to be treated with chlorine. So also,*a composite bleach solution of regulated permanganate and hypochlorite content can be made by dissolving known amounts of separately produced permanganate and hypochlorite. Such solutions can be produced prior to the addition of the composite bleaching solution to the pulp or other material to be bleached, or
.the mixture may be produced, for example,
in the pulp by separately adding the permanganate and hypochlorite solutions thereto, with appropriate agitation of the pulp to bring about uniformity of distribution of the reacting materials. The regulation of the proportions of permanganate and hypochlorite makes possible the regulation of the bleaching operation in a simple and advantageous manner, as will be readily appreciated.
\Vhen the pulp or other material to be washing the pulp or other material to be bleached, after the manggiiate orpermanganate and hypochlorite treatment, the pulp, etc., can be freed from the greater part of the compounds in solution, prior to the sulfur dioxide or other treatment for dissolving a manganese compound. Instead of using sulfur dioxide for converting a compound'of manganese into a soluble form, other agents. which convert such compound into colorless and soluble compounds can be similarly used. Acid alone can be used for this purpose, such as hydrochloric acid or sulfuric acid, but a considerable amount of such acid will-be re quired unless the action is carried out or finished at an elevated temperature, or allowed to stand for considerable time, and the fibres may be injured thereby. The treatment With sulfur dioxide or sulfurous acid has the advantage that it takes place readily and quickly at ordinary temperature.
WVhile we have described the invention more particularly in connection with the bleaching ofpulp, e. g., pulp derived-from wood, for which it is particularly advan tageous, yet it will be understood that the invention is also applicable to the bleaching of other fibrous materials, such as cotton, silk, linen, wool, etc., in a similar manner, as well as paper pulp stocks recovered through deinking processes, etc., and we include the bleaching of such materials within the more comprehensive claims appended hereto. Among the advantages of the process of the present invention is the uniformity of the bleaching action and the desirable condition in which the fibres are left. The fibres, for example, of cotton, silk, pulp, etc., are thus in a form well adapted for subsequenttreatment, e. g., for uniform dyeing, etc.
We have found that pulps obtained, for
example, by the soda, sulfate or sulfite process, so called, or modification thereof, are not only given a White color, but retain their white color much better and longer, when jected to a temperature of 100 C. for a period of seventy-two hours in the presence of air. This advantage of increased permanence of the whiteness of the bleached pulp is a characteristic advantage of the present invention.
It is a further advantage of the present invention that it makes possible the satisfactory bleaching of wood pulp cellulose produced by what is commonly known as theshorttime or quick-cook method, that is, by carry-- ing out the cook with cooking liquors of various degrees of strength or of concentration, at various pressures and temperatures and for various periods of time, and terminat ing the cook without carrying it to completion. Such pulp, produced by the short-time or quick-cook method, so-called, cannot be easily bleached by ordinary bleaching methods, and such treatment. usually gives a bleached product of inferior quality. We have found. however. that such pulp, which heretofore would be considered under-cooked and not easy to bleach by common bleaching methods, can advantageously be bleached by the process of the present invention and brought to a good white color with less injury to the fibres than with methods of bleaching heretofore commonly used. The present invention makes possible therefore theproduction of a satisfactory bleached pulp from under-cooked stock, thus avoiding the necessity in many cases of continuing the cooking operation for the normal period of time, etc. The cutting down of the time of the cooking operation makes possible an increase in the number of digestions which can be carried out in a given apparatus, and correspondingly increases the producing capacity of the digesters over the usual practice in the art. We accordingly include and claim as a part of our invention the production and bleaching of such under-cooked pulp by treating such pulp in the improved manner herein described.
In addition to the bleaching of undercooked pulps, the process of the present invention is also of particular value for the bleaching of chemical pulps from wood which are relatively difiicult to bleach by common bleaching methods and enables a superior bleached pulp to be obtained therefrom, of. good white color.
There are large supplies of forest products, etc., which, due to their inherent composition and properties, have been unsuited to the production of high grade cellulose material by the processes heretofore com monly practiced. We have foundthat many such materials can advantageously be treated for the production of pulp or cellulose materials by the use of a cookingliquor containing an alkali metal sulfite, with or without a lesser amount of other digesting reagent, as more fully described in companion applications. The bleaching process of the present invention is of special'value in conjunction with such a cooking process, and
gives a high grade white pulp from cellulose material. In this way cellulosic prod--- ucts such as wood, bagasse, reeds, grasses, bamboo, corn stalks, straws, etc., which are not commonly considered suitable for the production of high grade pulp or cellulose material can be converted into white products of relatively high grade. We therefore, have increased the available supply of raw materials available for the production of relativel high grade pulp or cellulose products. fiven when such products are subjected to the usual methods of cooking, the pulp obtained can be satisfactorily subjected to the bleaching process of the present invention to give a bleached pulp of high grade and whiter in color than is obtained with the usual bleaching processes, i. e., employing bleaching powder in the customary manner and amounts.
The process of the present invention, as above stated, is of moreor less general application to the bleaching of fibrous mate rial and. fabrics, etc., of a bleachable character and will give whiter bleached materials and with less injury than with any of the common bleaching methods of which we are aware.
While we have described the bleachin process of the present invention as carrie out with a manganate or permanganate, or
with acomposite bleach liquor containing both permanganate and hypochlorite, we-do not exclude the use of other bleaching agents, which may be used in conjunction with the manganate or permanganate. For
example, chlorine or a hypochlorite may be used to bring about a partial bleaching of the material, and the bleaching operation can then be completed with the manganate or permanganate, and, to the extent that residual chlorine or an active chlorine bearing compound remains when the manganate or permanganate is added, the further bleaching operation may be of a character similar to that when a composite bleach liquor containing permanganate and hypochlorite is added. So also, other bleaching agents may be used in conjunction with the manganate or perman anate, to modify the bleaching operation. Terborates or peroxides, for example, may thus be used.
While we have described the invention more particularly in connection with the use 7 of alkali metal and alkaline earth metal manga'na-tes and permanganates, the invention is not limited thereto, but other suitable manganates and permanganates can be used which are capable of exerting a bleaching or oxidizing action, and such manga'nates or permanganates can be used in conjunction with other agents, e. g., hypochlorites, etc., as hereinbefore described.
hen alkali metal manganates or permanganates are employed, they canbe produced by any suitable method of production, such as by fusion, electrolytically, etc. One advantageous method of production is by electrolyzing a solution of causticalkali or alkali metal carbonate, using anodes of ferromanganese or other suitable manganesebearing material. In preparing the manganate or permanganate solutions in this way, it is advantageous todiscontinue the electrolysis before all of the caustic alkali or alkali metal carbonate is converted into manganate or permanganate and to treat the resulting still alkaline solution with suitable chlorine bearing material to" form a composite bleaching liquor containing permanga nate and hypochlorite in solution.
In the accompanying claims we have used the phrase a manganate to include both manganates and permanganates. The term alkali-forming metal is intended to in-- clude both alkaline earth metals such as calcium, barium or magnesium and alkali metals such as sodium or potassium.
The broad invention describedherein as well as other specific inventions described but not claimed herein are claimed in our companion applications and patents Serial No. 449,245, filed March 2, 1921, which has matured into Patent No. 1,768,819, Serial No.
, 261,696, filed March 14, 1928, which has matured. into Patent No. 1,768,821, Serial No.
261,697, filedMarch 14,1928, which has matured into Patent No. 1,768,822, and Serial No. 544,322, filed March 16, 1922, which has matured into Patent No. 1,768,820. Other specific inventions for related subject mat-. ter are claimed in our application Serial No. 370,726, filed June 13, 1929, which has matured into Patent No. 1,768,823.
. We claim:
1. The process of bleaching pulp produced from wood by an incomplete digesting 1 treatment which comprises treating the resulting fibrous material by means of liquor supplied with a manganate and with alkali metal hypochlorite capable of exerting a bleaching action.
2. The process of treating cellulosic-fibrous material to obtain a product relatively high in alpha cellulose, which comprises subjecting wood pulp obtained from wood by a of chemical pulp from Wood, which comprises preparing a mixture containing such fibres and water, distributing throughout such mixture a solution containing an alkali metal. hypochlorite and a permanganate, treating the fibres by means of bleaching ma.- terials supplied by the solution until substantially all the colored. non-fibrous organic constituents of the pulp have been rendered substantially colorless or readily separable from the fibres, and subsequently treating the resulting fibrous material by means of an acid liquor so as to render soluble a colored tures.
LINN BRADLEY. EDWARD P. MQKEEFE.
we aflix our signatreatment in a liquor containing a sulfite of sodium, said treatment being insuificient to free the fibres fromallnon-cellulose material, to a treatment with a liquor supplied with a manganate of an alkali forming metal and an alkali metal hypochlorite.
3. The process of treating cellulosic=fibrous I material to obtain a product relatively high in alpha cellulose, which comprises subjecting wood pulp obtained from wood by a treatment in a liquor containing a sulfite of sodium, said treatment being insuflicient to free the fibres from allnon-cellulose material, to a treatment with a liquor supplied with a manganate of an alkali metal and an alkali metal hypochlorite until substantially all the colored non-fibrous organic constituents of the pulp have been rendered substantially colorless or are readily separable from the fibres of the pulp and subsequently treating the resulting fibrous material to". render soluble a compound of manganese.
4. The process of bleaching colored fibres
Priority Applications (1)
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US261698A US1795757A (en) | 1928-03-14 | 1928-03-14 | Method of bleaching and process for preparing liquors therefor |
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US261698A US1795757A (en) | 1928-03-14 | 1928-03-14 | Method of bleaching and process for preparing liquors therefor |
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US1795757A true US1795757A (en) | 1931-03-10 |
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US261698A Expired - Lifetime US1795757A (en) | 1928-03-14 | 1928-03-14 | Method of bleaching and process for preparing liquors therefor |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2492047A (en) * | 1946-03-30 | 1949-12-20 | Du Pont | Bleaching wood pulp |
US4083749A (en) * | 1975-07-23 | 1978-04-11 | Mitsubishi Chemical Industries Ltd. | Method of making sized paper |
US4141786A (en) * | 1976-09-13 | 1979-02-27 | International Paper Company | Manganic ion delignification of lignocellulosic material |
US5529697A (en) * | 1994-07-20 | 1996-06-25 | The University Of Southern Mississippi | Process for color removal from paper mill wastewaters |
-
1928
- 1928-03-14 US US261698A patent/US1795757A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2492047A (en) * | 1946-03-30 | 1949-12-20 | Du Pont | Bleaching wood pulp |
US4083749A (en) * | 1975-07-23 | 1978-04-11 | Mitsubishi Chemical Industries Ltd. | Method of making sized paper |
US4141786A (en) * | 1976-09-13 | 1979-02-27 | International Paper Company | Manganic ion delignification of lignocellulosic material |
US5529697A (en) * | 1994-07-20 | 1996-06-25 | The University Of Southern Mississippi | Process for color removal from paper mill wastewaters |
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