US1763368A - Method of accelerating and improving tanning processes - Google Patents
Method of accelerating and improving tanning processes Download PDFInfo
- Publication number
- US1763368A US1763368A US215761A US21576127A US1763368A US 1763368 A US1763368 A US 1763368A US 215761 A US215761 A US 215761A US 21576127 A US21576127 A US 21576127A US 1763368 A US1763368 A US 1763368A
- Authority
- US
- United States
- Prior art keywords
- tanning
- accelerating
- hides
- improving
- acid
- 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
- 238000000034 method Methods 0.000 title description 16
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 10
- 239000010985 leather Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 235000013311 vegetables Nutrition 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000284 extract Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 229960004592 isopropanol Drugs 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 238000006467 substitution reaction Methods 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- 229940013688 formic acid Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 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
- C14C3/10—Vegetable tanning
Definitions
- the hides are treated in tanning liquors, which have been enriched by means of nontanning substances (tannin, gallic acid, resorcin and the like) and are thereupon brought into strong tanning liquors, which are supposed to effect a thorough tanning of the hides in a short time.
- nontanning substances tanning liquors, which have been enriched by means of nontanning substances (tannin, gallic acid, resorcin and the like) and are thereupon brought into strong tanning liquors, which are supposed to effect a thorough tanning of the hides in a short time.
- the hides that is, the grained parts of the same are treated with inorganic salts adapted to make the grains non-sensitive to the astringent effects of strong tanning liquors (alumen, Glaubers salt, kitchen salt, bitter salt in combination with bichromate, boric acid, oxalic acid, chloride of calcium, hydrochloric aniline).
- strong tanning liquors alumen, Glaubers salt, kitchen salt, bitter salt in combination with bichromate, boric acid, oxalic acid, chloride of calcium, hydrochloric aniline.
- the first of the processes mentioned is expensive, and on account of the sensitivenessof the employed substances to iron, is not to be depended upon. Further the tanning lasts for at least 3 to 4 days, because the liquor at the first stages of treatment must not be stronger than 3 to 3 156. in order that the grains are not damaged.
- the initial treatment with inorganic salts is always risky, because conversion with the vegetable tanning agents may take place, whereby the coloring properties, the softness, the flexibility and the touch of the grains are ali'ccted in an unfavorable manner.
- chronilum salts and alumh num salts are used also the character of the leather is changed, so that a product is obtained, which resembles the so-called semichrome-leather.
- sul phonic acids which are obtained by condensing naphthalene or ring substitution productsof naphthalene, or the corresponding sulphonic acids, in the presence of condensation or oxidationv agents with alcohols of the aliphatic series, having more than two carbon atoms.
- Such substances may, for instance, be produced by converting one molecule of naphthulene into a mixture of alpha and beta. sulphonic acids and bringing the same into reaction with 2.1 molecules of isopropyl-alcohol and 221 molecules of concentrated sul 'ihurie acid at temperatures below 100 C. and in the presence of a large quantity ofconcentratcd sulphuric acid.
- the sodium salt obtained in the usual Way by treating with lime water and boiling the thus obtained sulphonic acid of the condensation product of naphthalene and iso-propyl alcbhol, forms directly a suitable addition for the tanning process to be described.
- naphthalene other polynuelear aromatic hydrocarbons and substitution products of such substances, as for instance, halogen or hydroxy substituted compounds, may be used.
- iso-propyl alcohol also higher alcohols especially such of the secondary series may be employed.
- the condensation products are amorphous substances which very easily dissolve in water and which as free acids and also as alkali salts possess a considerable moistening and frothing ability.
- hydrobeii zol Example 1 kg. of unhaired hides, which are designed for tanned upper leather and which, therefore, have been accordingly treated in the lime pit, are unlimed and eventually soaked. These hides are not as usual brought into a diluted color solution (tanning liquor of 0.5 to 1.5 136.) but are treated with a solution of 2 kg. of one of the above named substances in 300 liters of water for 3 to 4 hours, whereupon the hides are directly brought into a tanning liquor of 4 to 6 B., which is sufficiently strong to effect the final tannin
- the tanning may be performed in drums or rats.
- a tanning agent any vegetable extract or mixture of different extracts may be used. The entire tanning process lasts for 2a to 36 hours.
- Ewa-mple 2 100 kg. of unhaired hides, which are designed for bottom leather and have been accordingly treated, are unlimed as possible by means of an organic acid (lactic acid, formic-acid, butyric acid or the like) Thereupon 2 kg. of one of the above named substances are added to the same bath (or to a fresh bath) and are allowed to act upon the hides. For this purpose small amounts of organic acids may be added anew in order that the unhaired hides may be raised sufficiently. After 3 to L hours the hides can be put into the tanning bath. Any vegetable extract may be used. The extract is chosen in accordance with the purpose for which the finished product is intended to be used.
- an organic acid lactic acid, formic-acid, butyric acid or the like
- Example 3 The tr atment of unhaired hides can also ire performed in a weak tanning liquor to which 2 kg. of one of the above named substances are added for each 100 kg. of hides.
- a method of accelerating and improving the tanning processes when working with vegetable tanning agents which comprises adding to the tanning liquor, condensation products of naphthalene sulfonic acids and alcohols of the alipathic series having more than two carbon atoms in the presence of condensation mediums.
- a method of accelerating and improving the tanning processes when working with vegetable tanning agents which comprises adding to the tanning liquor sulphonic acids of propylated naphthalene.
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
lid
atented lune lmi lfl FRIEDRICH JPOSPIECH, OF DRESDEN, GERMANY, ASSIGNOR T0 CHIIEMJESCHE FABRIK IOT'JL d6 (30., OF DRIIE$DEN, GERMANY METHOD OF ACCELERATING AND IMPRUVING TAN'NING PROGESSES No Drawing. Application filed August 26, 1927, Serial No. 215,761, and in Germany August 21, 1926.
The hitherto employed tanning processes in which vegetable tanning principles are used are in general, very imperfect, because a very long time is needed for carrying out such processes and the coloring of leather produced in the known tanning processes is not always satisfactory. Normally, the tan ning of upper leather, which. has been pre liminary tanned in the usual ooze of M -2% Be. and has been finished in an ooze of (5 lie, lasts for at least 12 to 16 days. Several proposals have been madefor shortening the duration of the process but the quick-tanning methods hitherto proposed will not however give entirely satisfactory results, because the grains 'aretanned before the inner parts of the unhaired hides are tanned, whereby the grains are damaged and the surface of the leather assumes an unattractive look.
According to one quick-tanning method, the hides are treated in tanning liquors, which have been enriched by means of nontanning substances (tannin, gallic acid, resorcin and the like) and are thereupon brought into strong tanning liquors, which are supposed to effect a thorough tanning of the hides in a short time.
According to another proposal, the hides, that is, the grained parts of the same are treated with inorganic salts adapted to make the grains non-sensitive to the astringent effects of strong tanning liquors (alumen, Glaubers salt, kitchen salt, bitter salt in combination with bichromate, boric acid, oxalic acid, chloride of calcium, hydrochloric aniline).
The first of the processes mentioned is expensive, and on account of the sensitivenessof the employed substances to iron, is not to be depended upon. Further the tanning lasts for at least 3 to 4 days, because the liquor at the first stages of treatment must not be stronger than 3 to 3 156. in order that the grains are not damaged.
The initial treatment with inorganic salts, in accordance with the second of the above mentioned proposals, is always risky, because conversion with the vegetable tanning agents may take place, whereby the coloring properties, the softness, the flexibility and the touch of the grains are ali'ccted in an unfavorable manner. When chronilum salts and alumh num salts are used also the character of the leather is changed, so that a product is obtained, which resembles the so-called semichrome-leather.
l have now found, that the above mentioned drawbacks are avoided and the duraqualities superior to the leather hitherto obtained.
Especially suited for the purpose are sul phonic acids which are obtained by condensing naphthalene or ring substitution productsof naphthalene, or the corresponding sulphonic acids, in the presence of condensation or oxidationv agents with alcohols of the aliphatic series, having more than two carbon atoms.
Such substances may, for instance, be produced by converting one molecule of naphthulene into a mixture of alpha and beta. sulphonic acids and bringing the same into reaction with 2.1 molecules of isopropyl-alcohol and 221 molecules of concentrated sul 'ihurie acid at temperatures below 100 C. and in the presence of a large quantity ofconcentratcd sulphuric acid. The sodium salt, obtained in the usual Way by treating with lime water and boiling the thus obtained sulphonic acid of the condensation product of naphthalene and iso-propyl alcbhol, forms directly a suitable addition for the tanning process to be described.
Instead of naphthalene, other polynuelear aromatic hydrocarbons and substitution products of such substances, as for instance, halogen or hydroxy substituted compounds, may be used. Instead of iso-propyl alcohol also higher alcohols especially such of the secondary series may be employed. Further aliphatic and cyclic oletines, such as tetradissolved in concentrated sulphuric acid, are well suited for the purpose in question. The condensation products are amorphous substances which very easily dissolve in water and which as free acids and also as alkali salts possess a considerable moistening and frothing ability.
hydrobeii zol Example 1 kg. of unhaired hides, which are designed for tanned upper leather and which, therefore, have been accordingly treated in the lime pit, are unlimed and eventually soaked. These hides are not as usual brought into a diluted color solution (tanning liquor of 0.5 to 1.5 136.) but are treated with a solution of 2 kg. of one of the above named substances in 300 liters of water for 3 to 4 hours, whereupon the hides are directly brought into a tanning liquor of 4 to 6 B., which is sufficiently strong to effect the final tannin The tanning may be performed in drums or rats. As a tanning agent any vegetable extract or mixture of different extracts may be used. The entire tanning process lasts for 2a to 36 hours.
Ewa-mple 2 100 kg. of unhaired hides, which are designed for bottom leather and have been accordingly treated, are unlimed as possible by means of an organic acid (lactic acid, formic-acid, butyric acid or the like) Thereupon 2 kg. of one of the above named substances are added to the same bath (or to a fresh bath) and are allowed to act upon the hides. For this purpose small amounts of organic acids may be added anew in order that the unhaired hides may be raised sufficiently. After 3 to L hours the hides can be put into the tanning bath. Any vegetable extract may be used. The extract is chosen in accordance with the purpose for which the finished product is intended to be used.
Example 3 The tr atment of unhaired hides canalso ire performed in a weak tanning liquor to which 2 kg. of one of the above named substances are added for each 100 kg. of hides.
I claim 1. A method of accelerating and improving the tanning processes when working with vegetable tanning agents, which comprises adding to the tanning liquor, condensation products of naphthalene sulfonic acids and alcohols of the alipathic series having more than two carbon atoms in the presence of condensation mediums.
2. A method of accelerating and improving the tanning processes when working with vegetable tanning agents, which comprises adding to the tanning liquor sulphonic acids of propylated naphthalene.
FRI EUR [(H POSPIECH.
as completely
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1763368X | 1926-08-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1763368A true US1763368A (en) | 1930-06-10 |
Family
ID=7742259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US215761A Expired - Lifetime US1763368A (en) | 1926-08-21 | 1927-08-26 | Method of accelerating and improving tanning processes |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1763368A (en) |
-
1927
- 1927-08-26 US US215761A patent/US1763368A/en not_active Expired - Lifetime
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