US2265463A - Process to increase the viscosity of aqueous gelatin solutions - Google Patents
Process to increase the viscosity of aqueous gelatin solutions Download PDFInfo
- Publication number
- US2265463A US2265463A US339588A US33958840A US2265463A US 2265463 A US2265463 A US 2265463A US 339588 A US339588 A US 339588A US 33958840 A US33958840 A US 33958840A US 2265463 A US2265463 A US 2265463A
- Authority
- US
- United States
- Prior art keywords
- acid
- viscosity
- gelatin
- acids
- amino
- 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
- 108010010803 Gelatin Proteins 0.000 title description 28
- 229920000159 gelatin Polymers 0.000 title description 28
- 239000008273 gelatin Substances 0.000 title description 28
- 235000019322 gelatine Nutrition 0.000 title description 28
- 235000011852 gelatine desserts Nutrition 0.000 title description 28
- 238000000034 method Methods 0.000 title description 10
- 239000002253 acid Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 15
- -1 silver halide Chemical class 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 8
- 235000002639 sodium chloride Nutrition 0.000 description 7
- 125000004442 acylamino group Chemical group 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 2
- XMVQWNRDPAAMJB-UHFFFAOYSA-N (+)-13-Cyclopent-2-enyl-tridecansaeure Natural products OC(=O)CCCCCCCCCCCCC1CCC=C1 XMVQWNRDPAAMJB-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- XMVQWNRDPAAMJB-QGZVFWFLSA-N (S)-chaulmoogric acid Chemical compound OC(=O)CCCCCCCCCCCC[C@H]1CCC=C1 XMVQWNRDPAAMJB-QGZVFWFLSA-N 0.000 description 1
- XQITUXIEASXIMZ-UHFFFAOYSA-N 2-sulfooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O XQITUXIEASXIMZ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- UOWVXTFCPSXYLN-UHFFFAOYSA-N 3-amino-2-benzoylbenzoic acid Chemical compound NC1=CC=CC(C(O)=O)=C1C(=O)C1=CC=CC=C1 UOWVXTFCPSXYLN-UHFFFAOYSA-N 0.000 description 1
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- RRIWSQXXBIFKQM-UHFFFAOYSA-N benzylcarbamic acid Chemical compound OC(=O)NCC1=CC=CC=C1 RRIWSQXXBIFKQM-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Inorganic materials O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical class CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F4/00—Monocomponent artificial filaments or the like of proteins; Manufacture thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
- Y10S516/04—Protein or carboxylic compound containing
Definitions
- This invention relates to a process to increase the viscosity of aqueous gelatin solutions.
- the viscosity of aqueous gelatin solutions depends notoriously on several factors, as for instance gelatin quality, concentration, temperature, presence of hardeners and the like, and represents therefore a very variable indefinite quantity.
- To work up technical gelatin solutions for instance to spin filaments or to cast gelatin layers for the manufacture of foils or coatings for sizes, protective layers and the like, it is of great importance to adjust the viscosity independently of other factors influencing the viscosity and to have means at hand which make it possible to increase the viscosity in a regulatable and sufficient manner without noticeably influencing on the other hand the physical or chemical properties of the gelatin solution.
- An increase of the viscosity was hitherto accomplished by decreasing the temperature.
- the increase of the viscosity of such gelatin solutions in a manner sufiicient for all requirements may be accomplished according to the present invention by an admixture of acyl amino compounds of aromatic sulfoand carboxylic acids, in which the acyl radical consists of an aliphatic group of at least 10 carbon atoms or contains such a group.
- the aqueous solutions of these organic compounds show for themselves scarcely any higher viscosity than the solvent.
- the increase of the viscosity is therefore connected probably with a colloid chemical reaction which advantageously is so, that the usual properties of the gelatin are unchanged, when added in normal proportions.
- the naphthalene derivatives possess generally a higher effectiveness than the benzene derivatives.
- the disulfo acids are often more effective. than the monosulfo acids which also show reduced solubility. Also polyacids are very well suited.
- the sulfo acids may be employed also in the form of their salts or acid salts, if necessary together with organic bases. Their effectiveness is maintained also in various pH-regions. In the presence of soluble salts, for instance common salts, the effectiveness is somewhat decreased. The quantity of the admixture depends entirely on the desired effect. It is mostly suflicient to add 0.5-5% of the dry-weight of the gelatin, however more may be added.
- the atom groupings mentioned are also effective, when they are contained in the dyestuffs. Besides numerous other azo-dyestuifs the one obtained from tetrazotized diamino diphenyl eyclohexane and 1-stearoylamino-8-naphthol-fi-disulfo-acid increases also the viscosity of gelatin solutions.
- the radical of the stearic acid is of special interest, because it yields relatively high eflective compounds and also because the stearic acid is one of the cheapest of the respective acids.
- acids with less C-atoms as for instance palmitic acid, myristic acid, lauric acid are well suited as substituents, naturally also longer-chained acids like eicosane acid or montanic acids or unsaturated acids like the undecylic acid, oleic acid, eruic acid or also substitution products of these fatty acids, as for instance oxy compounds, halogen compounds and polyvalent acids like octadecyl dicarboxylic acid, sulfo stearic acid and others.
- the acids may also contain ring systems, as for instance the chaulmoogric acid or di-p-octadecyl benzoic acid.
- the fatty acid may also be connected by intermediate members with the benzeneor naphthalene sulfo acids, as for instance by the acid radical of amino fatty acids, aromatic amino acids (amino benzoic acid, amino benzoyl benzoic acid) or mixed aromatic-aliphatic acids like benzyl amino carboxylic acid, i. e. acyl amino groups and acid groups may belong also to different ring systems.
- Suitable compounds are for instance 2 stearoyl-amino-5-naphthol 7 sulfo-acid, 1- stearoyl amino 5 naphthol '7 sulfo-acid, 1- stearoyl amino 8 naphthol-3,6- disulfo acid, stearoyl-dehydrothio-p toluidinesulfo acid, 5- (m stearoylamino phenyl) -(naphtho-1',2' :2,3- imidazol) -5' ,7-disulfo-acid, l-(m-sulfo-phenyl) 3- (p-stearoyl-amino-phenyl) -pyrazolone- (5) 5- oleylamine-2,6-dimethylqulnoline 8 -sulfo-acid,
- Process for increasing the viscosity of aqueous solutions of gelatin which comprises adjusting the necessary viscosity to the desired degree by adding a substance selected from the class consisting of acyl-amino compounds of aromatic sulfo and carboxylic acids, in which the acyl radical consists of an aliphatic group of at least 10 carbon atoms.
- Process for increasing the viscosity of aqueous solutions of gelatin which comprises adjusting the necessary viscosity to the desired degree by adding a substance selected from the class consisting of acyl-amino compounds of aromatic sulfo and carboxylic acids, in which the acyl radical contains an aliphatic group of at least 10 carbon atoms.
- Process for increasing the viscosity of aqueous solutions of gelatin which comprises adjusting the necessary viscosityto the desired degree by adding a substance selected from the class consisting of acyl-amino compounds of arcmatic sulfo and carboxylic acids, in which the acyl radical contains the salts of an aliphatic group of at least 10 carbon atoms.
- Thickened aqueous solutions of gelatin containing an addition of a viscosity increasing agent selected from the class consisting of acylamino compounds of aromatic sulfoand carboxylic acids in which the acyl radicle consists of an aliphatic group of at least 10 carbon atoms.
- a viscosity increasing agent selected from the class consisting of acylamino compounds of aromatic sulfoand carboxylic acids in which the acyl radicle consists of an aliphatic group of at least 10 carbon atoms.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Materials For Medical Uses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2265463X | 1939-06-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2265463A true US2265463A (en) | 1941-12-09 |
Family
ID=7992979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US339588A Expired - Lifetime US2265463A (en) | 1939-06-03 | 1940-06-08 | Process to increase the viscosity of aqueous gelatin solutions |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2265463A (fr) |
| FR (1) | FR906016A (fr) |
-
1940
- 1940-06-08 US US339588A patent/US2265463A/en not_active Expired - Lifetime
-
1944
- 1944-07-21 FR FR906016D patent/FR906016A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR906016A (fr) | 1945-12-20 |
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