US2559305A - Manufacture of tanning substances - Google Patents
Manufacture of tanning substances Download PDFInfo
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- US2559305A US2559305A US9953A US995348A US2559305A US 2559305 A US2559305 A US 2559305A US 9953 A US9953 A US 9953A US 995348 A US995348 A US 995348A US 2559305 A US2559305 A US 2559305A
- Authority
- US
- United States
- Prior art keywords
- tanning
- substances
- parts
- alkali
- waste lye
- 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
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- 239000000126 substance Substances 0.000 title claims description 50
- 238000004519 manufacturing process Methods 0.000 title description 3
- 239000003513 alkali Substances 0.000 claims description 19
- 239000002699 waste material Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
- 239000000243 solution Substances 0.000 claims description 14
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 13
- 239000001913 cellulose Substances 0.000 claims description 9
- 229920002678 cellulose Polymers 0.000 claims description 9
- 239000012670 alkaline solution Substances 0.000 claims description 8
- 239000003518 caustics Substances 0.000 claims description 5
- 230000001376 precipitating effect Effects 0.000 claims description 4
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 53
- 235000011121 sodium hydroxide Nutrition 0.000 description 24
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 22
- 239000000203 mixture Substances 0.000 description 13
- 239000001569 carbon dioxide Substances 0.000 description 11
- 229910002092 carbon dioxide Inorganic materials 0.000 description 11
- 239000002253 acid Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 235000010265 sodium sulphite Nutrition 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000004291 sulphur dioxide Substances 0.000 description 2
- 235000010269 sulphur dioxide Nutrition 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 235000018553 tannin Nutrition 0.000 description 2
- 229920001864 tannin Polymers 0.000 description 2
- 239000001648 tannin Substances 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000836430 Hilda Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000218657 Picea Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- LVGQIQHJMRUCRM-UHFFFAOYSA-L calcium bisulfite Chemical compound [Ca+2].OS([O-])=O.OS([O-])=O LVGQIQHJMRUCRM-UHFFFAOYSA-L 0.000 description 1
- 235000010260 calcium hydrogen sulphite Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- -1 hydroxy- Chemical class 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- SYXUBXTYGFJFEH-UHFFFAOYSA-N oat triterpenoid saponin Chemical compound CNC1=CC=CC=C1C(=O)OC1C(C=O)(C)CC2C3(C(O3)CC3C4(CCC5C(C)(CO)C(OC6C(C(O)C(OC7C(C(O)C(O)C(CO)O7)O)CO6)OC6C(C(O)C(O)C(CO)O6)O)CCC53C)C)C4(C)CC(O)C2(C)C1 SYXUBXTYGFJFEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 238000004048 vat dyeing Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
- C14C3/08—Chemical tanning by organic agents
- C14C3/24—Chemical tanning by organic agents using lignin derivatives, e.g. sulfate liquor
Definitions
- the obtained tanning substance can be used by itself, without addition of other substances,
- the solution has a-pI-I-value of 3 to 4 and may be used according to the usual tanning prescriptions.
- the tanning substance is absorbed almost completely by the normally treated hides.
- the leather obtained is light-brown, has a slightly aromatic smell, good strength, and soft quality.
- a further advantage of our process consists in that owing to the careful low temperature treatment with alkali, not only the tanning substances of advantageous properties, but other valuable products can be obtained in the courseof this process. These products are destroyed -cOmpleteIy-orfor the greatest part, if tanning substances are obtained-from sulphite waste lye by a more intensive action of alkali.
- Such byiprod'ucts are, first of all, hydroxyand alkoxyaldehydes, especially vanillin, as well as sugar '..:acting' as a reducing agent, and organic acids.
- s-Hydroxyand alkoxy-aldehydes are obtained l.-.fr.om the mother liquor remaining after the separation of the tanning substance, according to methods knownper se, e. g. by extraction with organic solvents. or by steam distillation, a remaining solution rich in reducing, sugar-like :substances and organic acids being obtained.
- acid preferably hydrochloric acid
- acid is added in such an amount that only bisulphite and a small quantity of free sulphur dioxide are formed in the acidified mixture, whereas the presence of free mineral .acid is avoided, since such acid would decompose.
- the mother liquor deprived from the tan- ...ning substance is adjusted to a pH-value lower than 5, preferably to a pH-value between, 2 and 3.
- the aldehydes are obtained,
- the solution may be evaporated and the mineral salts, normally sodium chloride, may be obtained by crystallizing and centrifuging or the like.
- the separated salts may be used as tanning salts.
- greyish-brown color which still contains large sugar-like substances, as well as various organic acids and may be employed as a reducing agent for technical purposes, for instance to reduce metallic salts in galvanic processes, manufacture of dyes, vatdyeing and soon, and can substitute the substances, suchwas glucose, hyposulphite and the like-used heretofore inthese domains.
- organic dry substance of the sulphite cellulose waste lye or its residue which substance may, under normal tanning conditions, be employed as the only tanning means in the process.
- . ganic' dry substance are treated at normal temperature in a kneader with 40 parts of solid caustic soda which are gradually added. By proper. control of the alkali addition, a temperature of 90 to 100 C. is reached which .is
- Example 2 (2) 130 parts by weight of athickened spruce,- wood sulphite waste lye containing 34.7 per cent. organic dry substance are stirred at the conditions of the Example 1 with 67 parts by weight of per cent. strong lye at to C. for 6 to 8 hours, and the resultingmixture is worked up accordinging to Example 1.
- the yields amount to 30 parts by weight of tanning substance, 5 parts by weight of a mixture of aldehydes, 20 parts by weightofa reducing agent.
- the diluted solution resulting from the treatment of the sulphite waste lye or its residue with alkali is subjected to a saturation with carbon dioxide or gases containing carbon dioxide, before the taming substances are liberated by the acid treatment.
- the process is preferably carried out so that the saturation with carbon dioxide is effected in two stages by introducing first carbon dioxide, until a pH- value of 9 is attained; in this stage substantially sodium sulphite and sodium sulphate are precipitated together with slight amounts of soda.
- the saturation with carbon dioxide is continued in a second stage, until a pH-value of about 7.5 is reached.
- a mixture of bicarbonates with some soda precipitate is thus obtained, which includes at the same time a considerable amount of saponine substances of high lathering power, (fraction II)
- saponine substances of high lathering power fraction II
- the solution still contains the alkali compounds of the tanning substances, and, especially when working up beech-wood, considerable amounts of sodium acetate.
- the solution is now acidified, preferably up to a pH-value of 3.5 in a manner known per se.
- the acidification may be efiected by mineral acids, such as hydrochloric, sulphuric or phosphoric acid.
- mineral acids such as hydrochloric, sulphuric or phosphoric acid.
- sulphuric or phosphoric acid to liberate the tanning substances from their alkali compounds is particularly advantageous, since in such a case the liquid which is obtained, after the precipitated substances are filtered or centrifuged off, may be subjected to a distillation, if desired after being strongly acidified once more, in order to obtain acetic acid in the distillate.
- the carbon dioxide required in the course of the process for saturation and preliminary separation, is available in large quantities in paper mills and cellulose factories.
- the sulphite waste lye to be worked up accumulates, since in the manufacture of the waste lye of calcium bisulphite from lime stone and sulphurous acid, this lye bein used for disintegrating purposes, carbon dioxide escapes from the lye-towers as a waste gas.
- the mixture of sodium sulphite and sodium sulphate, accumulating as fraction I can be returned into the process by admixing this mixture of salts to the water in the lyetowers.
- a process for producing tannin substances from sulphite cellulose waste lye which comprises treating said waste lye in form of a concentrated liquor of about 30 B. with caustic alkali in a ratio of about 30-32 parts of caustic alkali, calculated a solid alkali hydroxide, per 100 parts of said concentrated liquor, said liquor containing from about 30-38 per cent of dry organic substances, maintaining the alkaline solution thus formed under atmospheric pressure at a temperature ranging from 60 to 100 C. for several hours, precipitating from the alkaline solution the tanning substances formed during the treatment by addition of hydrochloric acid in an amount imparting a pH-value of about 5 to the resulting liquid, and removing the tanning substances from said liquid.
- a process for producing tanning substances from sulphite cellulose waste lye which comprises treating said waste lye in form of a concentrated liquor of about 30 B. with concentrated caustic alkali at a temperature ranging from 60 to 100 C. for several hours under allmospheric pressure, precipitating from the alkaline solution the tanning substances formed during the treatment by addition of hydrochloric acid in an amount imparting to the resulting liquid a pH-value of about 5, removin the tanning substances from said liquid, adding more acid to bring the pH-value of the liquid to 2-3, and extracting therefrom the hydroxyand alkoxy-aldehydes present therein.
- a process for producing tanning substances 0 saturating the alkaline solution with carbon dioxide in two stages, introducing the carbon dioxide in a first stage until a pH-value of about 9 is reached in the solution, separatin from the liquid the formed mixture of sodium sulphite, sodium sulphate, and sodium carbonate, then from sulphite cellulose waste lye, which comintroducing carbon-dioxide in said second stage until-the pH-value reaches about 7.5, separating from the liquid the formed carbonates, bicarbonates, and saponine-like substances, there-- 4 after acidifying the liquid for precipitation of. the tanning substances and separating the same from the liquid.
- caustic soda is added in form of a concentrated solution of at least 60 per cent NaOI-I, in an amount of about 30-32 parts of NaOI-I for 100 parts of concentrated liquor.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Description
3. beech-wood sulphite waste lye of 33 Baum with 40 parts of solid caustic soda at 90 to 100 C., while stirring, for 6 to 8 hours.
The obtained tanning substance can be used by itself, without addition of other substances,
for tanning purposes and is practically com-- The process according to the invention has therefore the advantage of a practically complete utilization of the sulphite cellulose waste lye, since the following substances are obtained:
(a) A practically completely soluble tanning substance representing 60 to 70 per cent. of the pletely soluble in warm water with a yellow-" I brown color. The solution has a-pI-I-value of 3 to 4 and may be used according to the usual tanning prescriptions. The tanning substance is absorbed almost completely by the normally treated hides. The leather obtained is light-brown, has a slightly aromatic smell, good strength, and soft quality.
A further advantage of our process consists in that owing to the careful low temperature treatment with alkali, not only the tanning substances of advantageous properties, but other valuable products can be obtained in the courseof this process. These products are destroyed -cOmpleteIy-orfor the greatest part, if tanning substances are obtained-from sulphite waste lye by a more intensive action of alkali. Such byiprod'ucts are, first of all, hydroxyand alkoxyaldehydes, especially vanillin, as well as sugar '..:acting' as a reducing agent, and organic acids. s-Hydroxyand alkoxy-aldehydes are obtained l.-.fr.om the mother liquor remaining after the separation of the tanning substance, according to methods knownper se, e. g. by extraction with organic solvents. or by steam distillation, a remaining solution rich in reducing, sugar-like :substances and organic acids being obtained.
.- '..In order to avoid losses of hydroxyand alk- ..oxy+aldehydes when separating tanning substances from the mixture obtained by an alkali =.,treatment of the sulphite waste lye or the like at relatively low'temperatures, acid, preferably hydrochloric acid, is added in such an amount that only bisulphite and a small quantity of free sulphur dioxide are formed in the acidified mixture, whereas the presence of free mineral .acid is avoided, since such acid would decompose. the .bisulphite compounds of the hydroxyaand alkoxy-aldehydes split off from the lignin in.'the secondary reaction, and would result in -.a'iseparation of the aldehydes together with the ..tanning substance in insoluble form. The acidigfication of .the mixture for separating the tan- :ning substance is' therefore only carried to a pH-value of 5. Only after the separation of 5-; thetanning substance has occurred, the solution r...should be further acidified. If, for instance, an extraction process is used to obtain the aldehydes, the mother liquor deprived from the tan- ...ning substance, is adjusted to a pH-value lower than 5, preferably to a pH-value between, 2 and 3. Before, or after, the aldehydes are obtained,
. the solution may be evaporated and the mineral salts, normally sodium chloride, may be obtained by crystallizing and centrifuging or the like.
-The separated salts. may be used as tanning salts.
The residue which may be concentrated by evaporation at a suitable pI-I-value such as a pH- 1 value of 5, represents a rather'thick liquid of amounts of highly reducing,
greyish-brown color, which still contains large sugar-like substances, as well as various organic acids and may be employed as a reducing agent for technical purposes, for instance to reduce metallic salts in galvanic processes, manufacture of dyes, vatdyeing and soon, and can substitute the substances, suchwas glucose, hyposulphite and the like-used heretofore inthese domains.
organic dry substance of the sulphite cellulose waste lye or its residue, which substance may, under normal tanning conditions, be employed as the only tanning means in the process.
(1)) A large part of the sulphur contained in the initial material, particularly of the organ- Examples (1) 125 parts by weight Or thickened sulphite spirit residuec'ontaining 32.4 per. cent. or-
. ganic' dry substance, are treated at normal temperature in a kneader with 40 parts of solid caustic soda which are gradually added. By proper. control of the alkali addition, a temperature of 90 to 100 C. is reached which .is
maintained throughout the following 6 to '8 hours. .During that period, the mixture is being stirred and becomes thicker and darker. It
isthen diluted with water inthe amount of one third of the volume, whereafter a pI-I-value of 5 is adjusted with hydrochloric acid, the disengaged tanning substances are filtered off and washed in the cold with 0.5 per cent.. bydrochloric. acid and thereafter with water. 28 parts by weight of a dry tanning substance are 5 obtained. The mother liquor remaining from the filtration is mixed with the washing liquid and heated, while the escaping sulphur dioxide is collected. From'the remaining acid solution,
- in which the pH-value'is adjusted to 2-3, the
hydroxy-. and alkoxy-aldehydes liberated from their bisulphite compoundsfare obtained asyellow oils by known extraction methods with organic solvents (chloroform, ether, methylene chloride'and so on). The yield amounts to 3 parts by weight. The aqueous solution is then neutralized with alkali and concentrated by evaporationto. such'an extent that the dissolved sodium chloride is precipitated; There remain 18 parts by weight of a liquid which may be used as a reducing agent. r
(2) 130 parts by weight of athickened spruce,- wood sulphite waste lye containing 34.7 per cent. organic dry substance are stirred at the conditions of the Example 1 with 67 parts by weight of per cent. strong lye at to C. for 6 to 8 hours, and the resultingmixture is worked up acording to Example 1. The yields amount to 30 parts by weight of tanning substance, 5 parts by weight of a mixture of aldehydes, 20 parts by weightofa reducing agent.
(3) 128 parts of a thickened beech-wood sulphitewastelye containin 38 per cent. of organicdry substance arestirred. at the conditions of Example 1 with 40 parts ofsolidcaustic soda at 90 to 100 C; for 6 to 8.hours. By further working: up. the. resulting mixture according to Example l, 31 parts by weight of. a tanning substance; .8 parts by. weight ofa .mixture .of. alde-.
agent, are obtained.
hydes, and lfi -partsiby zweighigg of a reducing In 'order' to separate -the tanning, substances from the solution diluted with water; relatively large amounts'ofimineral. acids. are. consumed in, thisprocess, irrespective.,ot -.,-the particular.,con-
, -,ditions.maintained inthe, alkali treatment, since the entire amount of alkali .subjected'to'the reglaction must be combined withethe aci ,the tannin substance isliberated from its}.alkali m given 'in' the: gexamplesygper, ;1 parts zof;--,sul-
compounds. However, it. is possible to s,eparate the tanning substances from.,the solution-under conditions that will enableusto save, aponsid- .erable. amount of mineral acidgwith concurrent,
lrrinihezh e -imina r sepa atiomm ;sbemsedeas harmea se r,.asza cadd tio lWa hin lmeansaduerto ts c nte t. of rbona s, bicar- --cbona s.za drsanoni e like su s nc .ln; t e claims; sle res on' iconcent ated ncaustic. alkah. when ,noteoth w e. specified: i intended to define concentrations n ;the,;.;order .nofnabout .parts .brwe ht f;.=.caust c alka i (correspondin s sabo t parts vmmmen phite cellulose waste lye of,- about 30?,1,B..
Theexpre n:;su phi eece l ewwas esir ei th 1ai sis' n end dtold fl e aiconcen rated lawastezl sof .ahe tfi tjtBaum i lu ngswa t partial recovery of' the excessive alkali in fornr qgg lye residues whichmemainaitenthe extractiomof of valuable compounds.
For this purpose the diluted solution resulting from the treatment of the sulphite waste lye or its residue with alkali is subjected to a saturation with carbon dioxide or gases containing carbon dioxide, before the taming substances are liberated by the acid treatment. The process is preferably carried out so that the saturation with carbon dioxide is effected in two stages by introducing first carbon dioxide, until a pH- value of 9 is attained; in this stage substantially sodium sulphite and sodium sulphate are precipitated together with slight amounts of soda. After separating the mixture of salts (fraction I) the saturation with carbon dioxide is continued in a second stage, until a pH-value of about 7.5 is reached. A mixture of bicarbonates with some soda precipitate is thus obtained, which includes at the same time a considerable amount of saponine substances of high lathering power, (fraction II) By the described saturation with carbon dioxide and the preliminary separation of the precipitated salts, about two thirds of the alkali present are removed from the solution so that 40 the amount of mineral acid necessary for complete combination with the remainin alkali will be only one third of the amount required otherwise. After elimination of the salts formed in the reaction, the solution still contains the alkali compounds of the tanning substances, and, especially when working up beech-wood, considerable amounts of sodium acetate. For liberating the tanning. substances, the solution is now acidified, preferably up to a pH-value of 3.5 in a manner known per se. The acidification may be efiected by mineral acids, such as hydrochloric, sulphuric or phosphoric acid. The use of sulphuric or phosphoric acid to liberate the tanning substances from their alkali compounds is particularly advantageous, since in such a case the liquid which is obtained, after the precipitated substances are filtered or centrifuged off, may be subjected to a distillation, if desired after being strongly acidified once more, in order to obtain acetic acid in the distillate.
The carbon dioxide required in the course of the process for saturation and preliminary separation, is available in large quantities in paper mills and cellulose factories. There, the sulphite waste lye to be worked up accumulates, since in the manufacture of the waste lye of calcium bisulphite from lime stone and sulphurous acid, this lye bein used for disintegrating purposes, carbon dioxide escapes from the lye-towers as a waste gas. The mixture of sodium sulphite and sodium sulphate, accumulating as fraction I can be returned into the process by admixing this mixture of salts to the water in the lyetowers.
The mixture accumulating as fraction spirit or the like.
What- .we. cla rm-i 1. A procession pmducing tanning substances iromiesulphite cellulose. waste; lyemwhich-wcomprises treatin said waste lye in fOIIHsOi: arconcentrated liquor of about 30 B. with concentrated caustic alkali solution containing at least 60 per cent of alkali hydroxide, maintaining the alkaline solution under atmospheric pressure at 25 a temperature ranging from 60 to C. for
several hours, precipitating from the alkaline solution the tanning substances which formed during said treatment by addition of hydrochloric acid in an amount imparting a pH-value of about 5 to the resulting liquid, and removing the tanning substances from said liquid.
2. A process for producing tannin substances from sulphite cellulose waste lye, which comprises treating said waste lye in form of a concentrated liquor of about 30 B. with caustic alkali in a ratio of about 30-32 parts of caustic alkali, calculated a solid alkali hydroxide, per 100 parts of said concentrated liquor, said liquor containing from about 30-38 per cent of dry organic substances, maintaining the alkaline solution thus formed under atmospheric pressure at a temperature ranging from 60 to 100 C. for several hours, precipitating from the alkaline solution the tanning substances formed during the treatment by addition of hydrochloric acid in an amount imparting a pH-value of about 5 to the resulting liquid, and removing the tanning substances from said liquid.
3. A process for producing tanning substances from sulphite cellulose waste lye, which comprises treating said waste lye in form of a concentrated liquor of about 30 B. with concentrated caustic alkali at a temperature ranging from 60 to 100 C. for several hours under allmospheric pressure, precipitating from the alkaline solution the tanning substances formed during the treatment by addition of hydrochloric acid in an amount imparting to the resulting liquid a pH-value of about 5, removin the tanning substances from said liquid, adding more acid to bring the pH-value of the liquid to 2-3, and extracting therefrom the hydroxyand alkoxy-aldehydes present therein.
4. A process for producing tanning substances 0 saturating the alkaline solution with carbon dioxide in two stages, introducing the carbon dioxide in a first stage until a pH-value of about 9 is reached in the solution, separatin from the liquid the formed mixture of sodium sulphite, sodium sulphate, and sodium carbonate, then from sulphite cellulose waste lye, which comintroducing carbon-dioxide in said second stage until-the pH-value reaches about 7.5, separating from the liquid the formed carbonates, bicarbonates, and saponine-like substances, there-- 4 after acidifying the liquid for precipitation of. the tanning substances and separating the same from the liquid.
5. A process accordingto claim 4, wherein the caustic soda is added in form of solid NaOH in a ratio of about 30-32 parts to 100 parts of the concentrated liquor.
6.- A process according to claim 4, wherein the caustic soda is added in form of a concentrated solution of at least 60 per cent NaOI-I, in an amount of about 30-32 parts of NaOI-I for 100 parts of concentrated liquor.
MICHAEL MANGO-Ll).
, HILDA Administratrizc of the Estate of Fritz Neubyer,
Deceased.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Honig May 6, 1941
Claims (1)
1. A PROCESS FOR PRODUCING TANNING SUBTANCES FROM SULPHITE CELLULOSE WASTE LYE, WHICH COMPRISES TREATING SAID WASTE LYE IN FORM OF A CONCENTRATED LIQUOR OF ABOUT 30* BE. WITH CONCENTRATED CAUSTIC ALKALI SOLUTION CONTAINING AT LEAST 60 PER CENT OF ALKALI HYDROXIDE, MAINTAINING THE ALKALINE SOLUTION UNDER ATMOSPHERIC PRESSURE AT A TEMPERATURE RANGING FROM 60 TO 100* C. FOR SEVERAL HOURS, PRECIPITATING FROM THE ALKALINE SOLUTION THE TANNING SUBSTANCES WHICH FORMED DURING SAID TREATMENT BY ADDITION OF HYDROCHLORIC ACID IN AN AMOUNT IMPARTING A PH-VALUE OF ABOUT 5 TO THE RESULTING LIQUID, AND REMOVINGG THE TANNING SUBSTANCES FROM SAID LIQUID.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2559305X | 1944-05-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2559305A true US2559305A (en) | 1951-07-03 |
Family
ID=7996023
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US9953A Expired - Lifetime US2559305A (en) | 1944-05-02 | 1948-02-20 | Manufacture of tanning substances |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2559305A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2683706A (en) * | 1950-05-31 | 1954-07-13 | Inst Internat Financier | Method for the preparation of fusible lignin resins |
| US2727028A (en) * | 1951-03-14 | 1955-12-13 | Lignosol Chemicals Ltd | Treatment of waste sulphite liquor and products thereof |
| US3007864A (en) * | 1957-11-06 | 1961-11-07 | Puget Sound Pulp & Timber Co | Drilling muds and the like incorporating a treated sulfonated lignin containing material, and process for producing same |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US263797A (en) * | 1882-09-05 | Alexander mitscherlich | ||
| US940394A (en) * | 1908-09-24 | 1909-11-16 | Alexander Kumpfmiller | Tannin-containing extract and process of producing same. |
| US1147245A (en) * | 1914-02-26 | 1915-07-20 | Robeson Process Company | Tanning material and process of preparing the same. |
| US1303176A (en) * | 1919-05-06 | Ligno tanning material and process of producing the same from | ||
| US1571873A (en) * | 1924-06-10 | 1926-02-02 | Robeson Process Company | Process of making tanning preparations and products thereof |
| US1592062A (en) * | 1922-02-25 | 1926-07-13 | Baker Webster E Byron | Process for the conversion of sulphite waste liquors into tanning extracts |
| US1629448A (en) * | 1919-02-14 | 1927-05-17 | West Virginia Pulp & Paper Com | Process of making ligno-tanning material from waste sulphite liquor |
| US2241306A (en) * | 1936-07-09 | 1941-05-06 | Wilhelm Feith | Process for obtaining a tanning agent from waste sulphite liquor |
-
1948
- 1948-02-20 US US9953A patent/US2559305A/en not_active Expired - Lifetime
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US263797A (en) * | 1882-09-05 | Alexander mitscherlich | ||
| US1303176A (en) * | 1919-05-06 | Ligno tanning material and process of producing the same from | ||
| US940394A (en) * | 1908-09-24 | 1909-11-16 | Alexander Kumpfmiller | Tannin-containing extract and process of producing same. |
| US1147245A (en) * | 1914-02-26 | 1915-07-20 | Robeson Process Company | Tanning material and process of preparing the same. |
| US1629448A (en) * | 1919-02-14 | 1927-05-17 | West Virginia Pulp & Paper Com | Process of making ligno-tanning material from waste sulphite liquor |
| US1592062A (en) * | 1922-02-25 | 1926-07-13 | Baker Webster E Byron | Process for the conversion of sulphite waste liquors into tanning extracts |
| US1571873A (en) * | 1924-06-10 | 1926-02-02 | Robeson Process Company | Process of making tanning preparations and products thereof |
| US2241306A (en) * | 1936-07-09 | 1941-05-06 | Wilhelm Feith | Process for obtaining a tanning agent from waste sulphite liquor |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2683706A (en) * | 1950-05-31 | 1954-07-13 | Inst Internat Financier | Method for the preparation of fusible lignin resins |
| US2727028A (en) * | 1951-03-14 | 1955-12-13 | Lignosol Chemicals Ltd | Treatment of waste sulphite liquor and products thereof |
| US3007864A (en) * | 1957-11-06 | 1961-11-07 | Puget Sound Pulp & Timber Co | Drilling muds and the like incorporating a treated sulfonated lignin containing material, and process for producing same |
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