US1941475A - Bleached condensation product of carbohydrates and crude hydrocarbons - Google Patents
Bleached condensation product of carbohydrates and crude hydrocarbons Download PDFInfo
- Publication number
- US1941475A US1941475A US518291A US51829131A US1941475A US 1941475 A US1941475 A US 1941475A US 518291 A US518291 A US 518291A US 51829131 A US51829131 A US 51829131A US 1941475 A US1941475 A US 1941475A
- Authority
- US
- United States
- Prior art keywords
- condensation product
- bleached
- carbohydrates
- crude
- tanning
- 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
- 239000007859 condensation product Substances 0.000 title description 10
- 235000014633 carbohydrates Nutrition 0.000 title description 4
- 150000001720 carbohydrates Chemical class 0.000 title description 3
- 229930195733 hydrocarbon Natural products 0.000 title 1
- 150000002430 hydrocarbons Chemical class 0.000 title 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 16
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 229940099408 Oxidizing agent Drugs 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical class Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000007800 oxidant agent Substances 0.000 description 5
- 239000007844 bleaching agent Substances 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- 241000529895 Stercorarius Species 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- 239000005708 Sodium hypochlorite Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- 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 1
- 229910019093 NaOCl Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- -1 carbohydrates aromatic hydrocarbons Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001131 transforming effect Effects 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
- C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
- C14C3/20—Chemical tanning by organic agents using polycondensation products or precursors thereof sulfonated
Definitions
- oxidizingagent willnaturally varyito some-extent with the nature of the-condensation product-and its impuritles we "have found that in generalwi'th" condensation products contain-* January 31, 1931,condensation products ofcrude ing cellulose and residues'from tliepurific'ation m aromatic hydrocarbons or residues from the puricontain organic acids filed. January 31, 1931 andScrial- noisy 51 2,753-filed fication of aromatic hydrocarbons are condensed with carbohydrates'an'dsulfuric-acid or withcanbohydrates treated-with phthali'c' anhydrideand sulfuric acid, the products being tanningagents.
- tanning agents obtained by the sulfonation of crude aromatic hydrocarbons or other residues which are described in the co-pending application of J aeger and Witzel, Serial No. 518,- 292 filed February 25, 1931 are likewise very dark in color.
- Tanning agents obtained by the sulfonation of crude coal tar fractions such as anthracene oil, etc. may likewise be bleached by the process of the present invention.
- These tanning agents obtained by sulfonating crude coal tar fractions are described in the co-pending application of A. O. Jaeger, Serial No. 519,267 filed February 28,
- the condensation products may be bleached with oxidizing agents, for example hypochlorites, either in the preformed state or formed in situ by the use of chlorine, which decolorize the highly colored products, transforming them into relatively light colcred material, varying from a yellow to a light brown, which can be used even in the tanning of light coloredleathers and which show no no-.
- oxidizing agents for example hypochlorites
- Example 1 I 50 parts of the black granularmass obtained according to Example 1 of the Jaeger application Serial No. 512,500 filed January 30,1931 and which is the condensation product of the residue from the purification of crude anthracene by means of furfural, cellulose and sulfuric acid are mixed with 500 parts by weight of water and vigorously stirred for one hour. 400 parts of a water solution containing 10.84 parts of NaOCl is. vigorously stirred in. The stirring is continued for about two hours, the color of the liquor changing from dark brown or black to dark yellow or very light brown. On evaporation, a solid is obtained which is readily soluble in water.
- chlorine maybe passed in, the solution being kept sufficiently alkaline to assure good absorption of the chlorine.
- the amount of chlorine passed in man January 31, 1931, in the formof its sodium salt should, of course, correspond to about sodium hypochlorite.
- potassium permanganate or chromic acid may be used instead of using hypohalites.
- Example 2 A condensation product of cellulose treated with phthalic anhydride, the residue from the solvent purification of anthracene and sulfuric acid, prepared as described in Example 1 of the application of A. O. J aeger, Serial No. 512,753 filed is treated with a hypochlorite as described in Example 1. A very marked lightening in color is obtained without substantially affecting the tanning power of the material.
- Example 4 The condensation product of cellulose, the residue from the solvent purification of crude anthracene, sulfuric acid and formaldehyde,as
- Example 1 of theJaeger and Wit zel application Serial No. 518,292 filed February 25, 1931, above referred to, in the form or its sodium or calcium salt is treated with a hypochlorite as described in Example 1.
- the brownish black liquor is transformed into a light brown or brownish yellow, and retains its tanning powers.
- a process of producing light colored tanning agents which comprises condensing at least one carbohydrate, phthalic anhydride and at least one impure aromatic hydrocarbon with sulfuric acid and'subjecting ,a dispersion of the soluble condensation product obtained to the action oi a bleaching agent in amounts suflicient to substantially lighten the color, but insufficient to destroy the tanning properties thereof.
- a process of producing light colored tanning agents which comprises condensing at least one carbohydratawphthalic anhydride and at least one substance belonging to the group consisting of residues from solvent purification of crude anthracene with phenanthrene and carbazole solvents, residues from solvent purification of crude anthracene with phenanthrene solvents, residues from the vaporization of impure anthracene, residues from the vaporization of crude naphthalene, with sulfuric acid and subjecting a dispersion of the condensation product obtained to the action of a bleaching agent in amounts suiiicient to substantially lighten the color, but insuflicient to destroy the tanning properties thereof.
- a" V l 3.
- a process according to claim 1, in which the bleaching agent is a hypohalite.
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
aldehydes,"orboth.
In-co=pending applications of Jaeger, 'SerlaLNo. 512,500- filed January '30} 1931, Serial 'No. 512,752
Patented Jan. 2, 1934 lam-scum; CONBENSATIONWPRODUCT 0F omnenmnamsmnn @onomr omens Alphonso; ulian-Mount Lebanon, and-Heinrich I wzivnmmnaramma, assignorsto'lheselden. ('Jompany, Pittsburgh, Pa, a corporation 0t) l st m-m, ion February 19:11:
swarm. 518,291 I 4 (01., 260-2) Thi invention-relates to:condensation -prodnets of carbohydrates aromatic hydrocarbons and sulfuric acid which {may or may--not'- also such as phthalio'anhydride; I
. i amount of: oxidizingagent willnaturally varyito some-extent with the nature of the-condensation product-and its impuritles we "have found that in generalwi'th" condensation products contain-* January 31, 1931,condensation products ofcrude ing cellulose and residues'from tliepurific'ation m aromatic hydrocarbons or residues from the puricontain organic acids filed. January 31, 1931 andScrial- Noi 51 2,753-filed fication of aromatic hydrocarbons are condensed with carbohydrates'an'dsulfuric-acid or withcanbohydrates treated-with phthali'c' anhydrideand sulfuric acid, the products being tanningagents.
15 "While the tanning power of the products is excellent and-the raw-material lsf-very cheap, many of the products are open to the-objection that they are highly colored, this being particularly true of the products obtained from crude residues from the purification of aromatic hydrocarbons,
some of which are black orvery dark brown and are, therefore, objectionable when used with light colored leathers.
Similarly, tanning agents obtained by the sulfonation of crude aromatic hydrocarbons or other residues which are described in the co-pending application of J aeger and Witzel, Serial No. 518,- 292 filed February 25, 1931 are likewise very dark in color. The condensation products of cellulose, crude aromatic hydrocarbons and sulfuric acid when reacted with aldehydes as described and claimed in the application of Jaeger and Witzel,
' Serial No. 520,456 filed March 5, 1931 likewise present problems in tanning due to their high color.
Tanning agents obtained by the sulfonation of crude coal tar fractions such as anthracene oil, etc. may likewise be bleached by the process of the present invention. These tanning agents obtained by sulfonating crude coal tar fractions are described in the co-pending application of A. O. Jaeger, Serial No. 519,267 filed February 28,
, According to the present invention, we have found that, surprising as it may seem, the condensation productsmay be bleached with oxidizing agents, for example hypochlorites, either in the preformed state or formed in situ by the use of chlorine, which decolorize the highly colored products, transforming them into relatively light colcred material, varying from a yellow to a light brown, which can be used even in the tanning of light coloredleathers and which show no no-.
great excess oi oxidizing agent/"is used? If too- .large-an-excess of oxidizing agentis-used' the an 'ning power is lessened, and 'if' a sufilc'ient excess is used it may be-entirely destroyed; While the of aromatic hydrocarbonssuch as crude anthracene should not be treated with more than 50% of their weight of thefoxidizing agent'andusually 10% ives better results-1 I-naddition to the-hypohalites, other-oxidizing agents maybe'u'sed suchas chlorine in acid ;solution, chromic acidgpotassium pennanganateyetc and; ifdsiredymixturesmaybe used: Irr'case' of chromic acid, the reduction product is itself a tanning material.
The constitution of the condensation products involved in the present invention is not definitely known and the action of the oxidizing agent is likewise not definitely proven. Nevertheless, we
Example 1 I 50 parts of the black granularmass obtained according to Example 1 of the Jaeger application Serial No. 512,500 filed January 30,1931 and which is the condensation product of the residue from the purification of crude anthracene by means of furfural, cellulose and sulfuric acid are mixed with 500 parts by weight of water and vigorously stirred for one hour. 400 parts of a water solution containing 10.84 parts of NaOCl is. vigorously stirred in. The stirring is continued for about two hours, the color of the liquor changing from dark brown or black to dark yellow or very light brown. On evaporation, a solid is obtained which is readily soluble in water. and shows good tanning powers Instead of using sodium hypochlorite, chlorine maybe passed in, the solution being kept sufficiently alkaline to assure good absorption of the chlorine. The amount of chlorine passed in man January 31, 1931, in the formof its sodium salt should, of course, correspond to about sodium hypochlorite.
Instead of using hypohalites, potassium permanganate or chromic acid may be used.
Example 2 Example 3 A condensation product of cellulose treated with phthalic anhydride, the residue from the solvent purification of anthracene and sulfuric acid, prepared as described in Example 1 of the application of A. O. J aeger, Serial No. 512,753 filed is treated with a hypochlorite as described in Example 1. A very marked lightening in color is obtained without substantially affecting the tanning power of the material.
Example 4 The condensation product of cellulose, the residue from the solvent purification of crude anthracene, sulfuric acid and formaldehyde,as
adescribed in Example 1 of theJaeger and Wit zel application Serial No. 518,292 filed February 25, 1931, above referred to, in the form or its sodium or calcium salt is treated with a hypochlorite as described in Example 1. The brownish black liquor is transformed into a light brown or brownish yellow, and retains its tanning powers.
What is claimed as new is: 1. A process of producing light colored tanning agents, which comprises condensing at least one carbohydrate, phthalic anhydride and at least one impure aromatic hydrocarbon with sulfuric acid and'subjecting ,a dispersion of the soluble condensation product obtained to the action oi a bleaching agent in amounts suflicient to substantially lighten the color, but insufficient to destroy the tanning properties thereof.
2. A process of producing light colored tanning agents, which comprises condensing at least one carbohydratawphthalic anhydride and at least one substance belonging to the group consisting of residues from solvent purification of crude anthracene with phenanthrene and carbazole solvents, residues from solvent purification of crude anthracene with phenanthrene solvents, residues from the vaporization of impure anthracene, residues from the vaporization of crude naphthalene, with sulfuric acid and subjecting a dispersion of the condensation product obtained to the action of a bleaching agent in amounts suiiicient to substantially lighten the color, but insuflicient to destroy the tanning properties thereof. a" V l 3. A process according to claim 1, in which the bleaching agent is a hypohalite.
;4. A process according to claim 2, in which the bleaching agent is a hypohalite.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US518291A US1941475A (en) | 1931-02-25 | 1931-02-25 | Bleached condensation product of carbohydrates and crude hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US518291A US1941475A (en) | 1931-02-25 | 1931-02-25 | Bleached condensation product of carbohydrates and crude hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1941475A true US1941475A (en) | 1934-01-02 |
Family
ID=24063327
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US518291A Expired - Lifetime US1941475A (en) | 1931-02-25 | 1931-02-25 | Bleached condensation product of carbohydrates and crude hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1941475A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9296956B2 (en) | 2010-10-28 | 2016-03-29 | Chevron U.S.A. Inc. | Method for reducing mercaptans in hydrocarbons |
-
1931
- 1931-02-25 US US518291A patent/US1941475A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9296956B2 (en) | 2010-10-28 | 2016-03-29 | Chevron U.S.A. Inc. | Method for reducing mercaptans in hydrocarbons |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1941475A (en) | Bleached condensation product of carbohydrates and crude hydrocarbons | |
| US2168315A (en) | Method for the purification of petroleum mahogany sulphonates | |
| US2000244A (en) | Process for separation and recovery of naphthenic acids and phenols | |
| US2058911A (en) | Process for the purification of naphthylamine sulphonic acid | |
| US1806973A (en) | Irvin w | |
| US2223364A (en) | Method of producing higher alkyl aromatic sulphonates | |
| US2121845A (en) | Process for producing clear lightcolored, water-soluble sulphonation products of mineral oil | |
| US2071521A (en) | Production of fluorescence producing substances soluble in hydrocarbon oils | |
| DE2346230A1 (en) | Process for the production of a starting material for activated carbon and its use for the production of activated carbon | |
| US745802A (en) | Nitro product. | |
| US2121032A (en) | Detergent and wetting agent and process of producing the same | |
| US518990A (en) | Hans a | |
| US1848883A (en) | Joseph bennett hill | |
| US1557844A (en) | Tanning composition | |
| US2346524A (en) | Production of thiophene-free benzene | |
| DE647988C (en) | Process for the preparation of condensation products containing sulfuric acid residues | |
| DE544889C (en) | Process for the preparation of sulfonic acids from condensation products from polynuclear aromatic hydrocarbons and olefins | |
| US972953A (en) | Slovent for pyroxylin, &c., and process for making the same. | |
| US3030410A (en) | Preparation of oil soluble sulfonates | |
| US1309320A (en) | Eiilis | |
| US1305790A (en) | forrest | |
| US2108901A (en) | Production of assistants for the | |
| US1595455A (en) | Process for treating petroleum emulsions | |
| US1708103A (en) | Signors to l g | |
| US54267A (en) | Improved method of purifying hydrocarbon oils |