US3194865A - Acid depilation and extrudable fibril production from hide corium - Google Patents
Acid depilation and extrudable fibril production from hide corium Download PDFInfo
- Publication number
- US3194865A US3194865A US227585A US22758562A US3194865A US 3194865 A US3194865 A US 3194865A US 227585 A US227585 A US 227585A US 22758562 A US22758562 A US 22758562A US 3194865 A US3194865 A US 3194865A
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- Prior art keywords
- hide
- corium
- acid
- collagen
- solution
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- Expired - Lifetime
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- 239000002253 acid Substances 0.000 title claims description 54
- 238000004519 manufacturing process Methods 0.000 title description 8
- 230000035617 depilation Effects 0.000 title 1
- 102000008186 Collagen Human genes 0.000 claims description 66
- 108010035532 Collagen Proteins 0.000 claims description 66
- 229920001436 collagen Polymers 0.000 claims description 66
- 239000000243 solution Substances 0.000 claims description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 210000002615 epidermis Anatomy 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 19
- 239000007864 aqueous solution Substances 0.000 claims description 17
- 230000001112 coagulating effect Effects 0.000 claims description 17
- 210000004907 gland Anatomy 0.000 claims description 16
- 238000001035 drying Methods 0.000 claims description 14
- 238000005406 washing Methods 0.000 claims description 14
- 239000012670 alkaline solution Substances 0.000 claims description 9
- 238000002791 soaking Methods 0.000 claims description 9
- 210000001732 sebaceous gland Anatomy 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- 239000000701 coagulant Substances 0.000 claims description 7
- 210000004207 dermis Anatomy 0.000 claims description 7
- 238000007790 scraping Methods 0.000 claims description 6
- 241001465754 Metazoa Species 0.000 claims description 5
- 210000004209 hair Anatomy 0.000 description 18
- 238000011282 treatment Methods 0.000 description 16
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 10
- 235000011941 Tilia x europaea Nutrition 0.000 description 10
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 10
- 235000011130 ammonium sulphate Nutrition 0.000 description 10
- 238000001125 extrusion Methods 0.000 description 10
- 239000000835 fiber Substances 0.000 description 10
- 239000004571 lime Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 229940037003 alum Drugs 0.000 description 9
- 230000003750 conditioning effect Effects 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 102000011782 Keratins Human genes 0.000 description 8
- 108010076876 Keratins Proteins 0.000 description 8
- 238000010494 dissociation reaction Methods 0.000 description 8
- 230000005593 dissociations Effects 0.000 description 8
- 210000003780 hair follicle Anatomy 0.000 description 8
- 210000003491 skin Anatomy 0.000 description 8
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 6
- 239000001768 carboxy methyl cellulose Substances 0.000 description 6
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 6
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 6
- 229940105329 carboxymethylcellulose Drugs 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000006386 neutralization reaction Methods 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 239000011260 aqueous acid Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 4
- 238000010306 acid treatment Methods 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000010985 leather Substances 0.000 description 4
- 235000013580 sausages Nutrition 0.000 description 4
- 241000283690 Bos taurus Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 229940093915 gynecological organic acid Drugs 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- BSYNFGPFPYSTTM-UHFFFAOYSA-N 2-hydroxypropanoic acid;hydrate Chemical compound O.CC(O)C(O)=O BSYNFGPFPYSTTM-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 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
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009937 brining Methods 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 230000006240 deamidation Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003307 slaughter Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 230000003313 weakening 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
- C14C1/00—Chemical treatment prior to tanning
- C14C1/06—Facilitating unhairing, e.g. by painting, by liming
-
- A—HUMAN NECESSITIES
- A22—BUTCHERING; MEAT TREATMENT; PROCESSING POULTRY OR FISH
- A22C—PROCESSING MEAT, POULTRY, OR FISH
- A22C13/00—Sausage casings
- A22C13/0013—Chemical composition of synthetic sausage casings
- A22C13/0016—Chemical composition of synthetic sausage casings based on proteins, e.g. collagen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L89/00—Compositions of proteins; Compositions of derivatives thereof
- C08L89/04—Products derived from waste materials, e.g. horn, hoof or hair
- C08L89/06—Products derived from waste materials, e.g. horn, hoof or hair derived from leather or skin, e.g. gelatin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09H—PREPARATION OF GLUE OR GELATINE
- C09H1/00—Pretreatment of collagen-containing raw materials for the manufacture of glue
- C09H1/04—Pretreatment of collagen-containing raw materials for the manufacture of glue of hides, hoofs, or leather scrap
Definitions
- the collagen fibrils in bovine hides are arranged in bundles to form collagen fibers that vary in length and measure many thousand of Angstroms in diameter.
- Cowhide collagen fibers have been observed which measure about 10,000 to 20,000 Angstroms in diameter in the dehydrated state but larger collagen fibers measuring as much as 1,000 microns in diameter in their dehydrated state are believed to exist.
- Each collagen fiber contains hundreds or even thousands of fibrils, all bound together by a sheath.
- the collagen fibers in turn are organized into bundles of ollagen fibers that are large enough to be seen by the naked eye and form the familiar fibers visible in hides of all sorts.
- cowhide tissue is the commercially available raw material from which collagen fibrils can be obtained.
- Edible sausage casings may be manufactured by extruding a mass of undegraded acid swollen collagen fibrils through an annular orifice to form a tubular casing which can then be treated in a manner to dehydrate and deswell the individual collagen fibril units.
- collagen fibrils in the extruded casing lose their excess water of hydration by air drying, they cohere to form a translucent hyaloid substance in which the boundary line between individual fibrils cannot be distinguished.
- the hide To make a dispersion of swollen collagen fibrils suitable for extrusion, the hide must first be freed from all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands. This upper portion of the hide has been aptly designatetd the thermostat layer by Wilson, since it contains those organs concerned with the regulation of body temperature. These structures are made up of proteins of the class known as keratin.
- the class of protein known as collagen is present in that part of the hide lying beneath the thermostat layer, known as the corium.
- Centuries ago tanners discovered that a solution of lime might be used to separate hair from skin without much damage to the skin. The reason for this is that lime has a limited saturability. If one pound of lime (calcium hydroxide) is put into a gallon of water, from 99.4 to 98.5 percent of it will remain undissolved because the solution becomes saturated at about 0.006 pound per gallon of water at boiling point and at about 0.015 pound per gallon of water near the freezing point. A saturated solution of lime has a pH value of about 12.5. It cannot be raised above this point by adding more lime because the excess will not dissolve.
- calcium hydroxide calcium hydroxide
- lime treatment is quite suitable for leather manufacture, lime should not be used to dehair hides if the end product is to be an extruded casing.
- lime aids in the removal of hair and the epidermis layer like most chemical reactions the liming of hides requires judgment and some compromise because the reaction of lime with keratin and collagen is not perfectly selective.
- the liming of hides is a very complicated reaction chemically which can effect the collagen fibrils that make up the hide in at least three ways:
- Calcium hydroxide has a specific effect on collagen and a tendency to form complexes with hydroxy groups, which probably is connected with its low degree of ionization, its complexing power, and the bivalency of the cation.
- bovine hides are dehaired in such a way that the corium is not adversely affected for its subsequent use in the preparation of swollen collagen fibrils for casing manufacture.
- This may be accomplished by soaking the hide in a dilute aqueous solution of a weak acid that has a dissociation constant between l.O l0- and 1.0 10 in aqueous solutions. That one should in this manner be able to facilitate the removal of hair and epidermis without adversely effecting the collagen fibrils that make up the corium is all the more surprising in view of the known greater resistance of keratin to acid attack.
- the hairs are rendered removable from the skin by the dilute acid treatment because the acid swells and softens the corium of the skin, thus rendering the-hairs removable from the follicles and the epidermis removable from the collagencontaining derma.
- the subsequent treatment of the corium to produce swollen collagen fibrils for casings involves further swelling with similar dilute solutions of weak acids, the unhairing of the hides with such acid solutions is not adverse to the subsequent treatment of the corium and in some cases may contribute favorably to such subsequent treatment.
- Weak organic acids which may be used in the practice of the present invention are those having a dissociation is difficult to pass through the rollers of the splitting and dehairing machine. 7
- the acidic aqueous solutions used may contain from 3 to 5% by weight of the organic acids described above, as required to give a pH of 2.3 to 3.7.
- the acidic dehairing solution should be maintained at room temperature (about 7075 F.) and the fresh hides are permitted to soak in the acid bath with occasional agitation for 100 to 150 hours. The soaking'time in the bath may, of course, be reduced if the temperature of the bath is increased, but at elevated temperatures there will be some loss of the collagen due to acid hydrolysis and degradation.
- the hides after this acid treatment are run through a defleshing machine and scraped on both sides to remove all hair epidermis and any adhering flesh.
- the cleaned corium so obtained is in a swollen condition because of Lsolvation that occurs during the acid treatment. This swelling interferes with cornminution and other mechanical handling of the skin during the preliminary stages of dispersing the collagen fibrils. It is necessary, therefore, after removal of the hair and epidermis to carefully neutralize and deswell the cleaned hide corium before proceeding further.
- the cleaned hide corium is soaked in a weak aqueous alkaline bath at room temperature for about 12 hours. It is important to control the temperature and pH of the neutralizing bath to avoid alteration or degradation of the collagen.
- the alkaline bath should not contain reagents, such as lime, or alkaline earth salts that might form an irreversible complex with the collagen.
- the alkaline bath may be prepared by dissolving ammonia or a soluble salt of a strong base and a weak acid, such as sodium bicarbonate, in water to give an alkaline pH below 10.0. Strongly alkaline agents must be avoided with regard to the ultimate use of the corium because the reagent used for neutralization and the ultimate pH of the neutralized skin are of. substantial importance as they effect the subsequent condition of the acid swollen collagen fibrils in the mass to be extruded.
- the cleaned hide corium is Washed in Water for 3 to 4 hours.
- the hide corium after neutralization and washing is in a deswollen condition and may be subdivided, using conventional grinding equipment, to a particle size that is readily dispersible in dilute acid solution.'
- the cleaned hide corium is then loaded into a large drum having a capacity for forty hides and carefully neutralized by washing for four hours at a temperature of 55410" F. in a dilute alkaline solution containing eighty pounds of sodium bicarbonate in 4,000 pounds of water. The total time required for neutralization in this alkaline wash is approximately 12 hours.
- the neutralized hide corium is next washed in an overflow'bath for 3 to 4 hours in order to remove the salts formed during the neutralization step.
- the hide corium afte this final Wash is composed of substantially pure colagen fibrils free of all hair follicles and other extraneous matter. It may be comrninuted and reswollen in acid solution to form a homogeneous mass of swollen collagen fibrils useful in the manufacture of extruded collagen casings, as disclosed, for example, in United States Patents No. 3,123,653 and No. 3,123,482.
- Composites are prepared from five hides; The hide composites are then cut into /2 to 4 square inch sections and reduced to pulp by three passes through a meat grinder, each pass being a finer grind. The first and second passes are through 18 and 8 millimeter holes, respectively. The final grind is through holes 1.5 millimeters in diameter. ltis important during the grinding process to keep the pulp below 20 C. This may be done by adding crushed ice to the hide sections as they are fed to the grinder.
- the ground pulp is next diluted with tap water at 16 C. to give a smooth slurry containing 7.4% dry solids.
- This slurry parts is then treated with 125 parts of a 2.4% lactic acid water solution using an inline mixer to form a homogeneous mass of swollen colagen fibrils. It is important during this acid swelling step also that the temperature be maintained below about 25 C.
- the mixture so obtained contains 3.7% hide solids and 1.2% lactic acid.
- the mass of swollen collagen fibrils is further dispersed in a suitable homogenizer, fitted with a 2-stage valve and operated with a 1500 p.s.i. drop per stage.
- the individual fibrils are freed from the fiber bundles and fibers and released from'the fiber sheaths. They take up all liquid and swell from an original diameter of the order of 300 A. to 1000 A. toa freshly swollen (one day old) maximum diameter of the order of 15,000 A.
- mixtures prepared in similar manner may contain hide solids (in the above-described form of swollen collagen fibrils)'as low as about 3% and as high as about 5%, the preferred concentration of hide solids being about 4%. If the concentration is less than 2.5% the mixture is so watery that coagulation after extrusion becomes virtually impossible, while a concentration exceeding 6% requires very high extrusion pressures due to increased viscosity and tends to formation of tough casings.
- the preferred concentration of lactic acid is about 1.2% but may be as low as about 0.50%.
- the fluid mass of swollen collagen fibrils obtained by the method above described is filtered through a 7-mil filter screen to remove unswollen collagen and noncolagenous materials, and then extruded in the form of a tube preferably in such away as to impart some collagen fibril orientation transverse to the extrusion direction.
- extruder constitutes no essential part of the present invention, but it has been found preferable to utilize the action of the extruder to effect the maximum homogeneity of fibril distribution so as to impart substantial burst strength and transverse tear strength to the tube and horre casing while also eifectingorientation or alignment of fibrils or masses of fibrils in the direction of extrusion, particularly those adjacent the tube walls, thereby to achieve substantial longitudinal or tensile strength as well.
- the extruded fluid mass of swollen collagen fibrils leaves the orifice of the extruder in the form of a tubular body of Watery fluid travelling preferably upwardly into a dehydrating or coagulating bath which surrounds the orifice of the extruder and extends upwardly therefrom.
- the initial coagulating bath into which the extruded tubular body immediately passes is preferably in the form of a vertical column of liquid constituting a housing surrounding and extending upwardly from the extruder orifice. A portion of this liquid flows upwardly within the extruded tubular body, passing between the extruded body and an internally disposed over-fiow or return tube.
- the flow rate within the extruded body is quite slow, to avoid pressures and velocities harmful to the delicate extruded body, and may be, e.g., about 1 gallon per hour.
- Another portion of the coagulating liquid flows upwardly in the housing outside the extruded tubular body and returns through an external overflow drain for recirculation.
- the fiow rate of said outside column of liquid may be relatively rapid, e.g., about 2 gallons per minute.
- the density of the extruded tubular body as it comes from the extruder orifice is substantially less than that of the coagulating salt solution into which it passes. Accordingly the tendency of the extruded tubular body is to rise and travel naturally upwardly in the coagulating liquid. This phenomenon facilitates the starting up of the extruder and the maintenance of the desired upward travel of the-tubular body with the exertion of a minimum of external forces thereupon. This action occurs at that stage in the treatment of the tubular body when it is weakest and most fragile and possesses virtually no integrity of its own.
- This coagulating treatment is the first conditioning step applied afte extrusion of the tubular body.
- the extended coagulating bath itself is preferably an aqueous ammonium sulfate solution containing about 40% ammonium sulfate adjusted to a pH substantially higher than that of the acidswollen collagen material, e.g., a pH of about 7.0, with some suitable alkaline material such as sodium or ammonium hydroxide.
- the coagulating liquids in the vertical housing above the extruder and in said extended bath are of the same aforesaid composition.
- the purpose served by these coagulating baths is primarily to replace the water in the extruded tubular body by ammonium sulfate solution, thereby coagulating and giving temporary form and integrity to the tubular body so that it may be handled in the subsequent conditioning operations.
- the tubular body when it passes from the extrusion nozzle or orifice, has a wall thickness determined by the annular space between the internal and external extruder tubes forming the orifice.
- the external diameter of the inner extrusion tube is preferably about .75 while the radial distance between the exterior of said inner tube and the interior wall of the external tube is about .014".
- the tubular body referred to will have an initial wall thickness of about .014" (14 mils) and this thickness will be substantially maintained throughout most of the liquid conditioning treatments as hereinafter described.
- the dried tubular body will be reduced to a wall thickness of the order of .001" (1 mil), but the initial inne diameter of about .75 will be preserved.
- the casing diameter of about .75" is typical of casings used for fresh pork sausages.
- the concentration of coagulating salt in the coagulated tubular body is substantially reduced, thereby to facilitate the hardening action ereinafter described.
- hardening is effected by treatment with alum and it has been found that such treatment is effective only when the concentration of ammonium sulfate in the tubular body has been substantially reduced, yet a sufiicient amount thereof retained pro term to avoid undue softening and weakening of the coagulated tubular body. Accordingly the tubula body is pro-washed for a period of about six minutes in a much diluted water solution of ammonium sulfate (e.g., about 4% to 18%) similarly adjusted to pH of about 6.5.
- a third conditioning step constitutes a hardening of the coagulated casings by reaction of the collagen therein to alum.
- the pre-washed coagulated tubular body is immersed in and treated with a solution containing, e.g., about 6% alum [NH Al(SO -24H O], 1% citric acid and 4% ammonium sulfate.
- the contact time is about six minutes and this alum hardening solution is maintained at pH 4.3.
- This hardening treatment is sometimes called tanning, but the primary purpose is to efiect a hardening of the casing so as to make it resistant to water, which is not the case with collagen coagulated with ammonium sulfate. Without such hardening action the application of water to the tubular body coagulated with ammonium sulfate would reduce it to a formless gel. In other words the coagulation with ammonium sulfate is essentially a temporary step after which a more permanent hardening action is effected by treatment with alum. More detailed descriptions of the alum treatment with various examples thereof are given in United States Patent No. 3,123,481.
- the fourth conditioning step involves removal of the ammonium sulfate salt which has remained in the tubular body after the pre-wash and alum hardening "steps. This excess am monium sulfate as well as any excess alum in the tubular body are removed by a prolonged washing of the tubular body in tap water, e.g., for about twenty minutes, preferably using two or more changes of water.
- the fifth step in the conditioning of the tubular body is called a plasticizing operation.
- This procedure involves essentially two steps, one of which is the application of a humectant such as glycerine which preserves the softness of the material after drying and helps in rehumidifying it.
- a humectant such as glycerine which preserves the softness of the material after drying and helps in rehumidifying it.
- This plasticizing material also prevents cracking and other effects consequent upon undue drying.
- the plasticizing bath may contain 3.6% glycerol, 20 parts per million formaldehyde and 0.1% sodium bicarbonate. The dwell time in this bath is about five minutes.
- CMC carboxymethyl-cellulose
- the plasticizing bath Concomitantly with the plasticizing step, carboxymethyl-cellulose (CMC) is preferably included in the plasticizing bath and applied thereby to the tubular body.
- CMC carboxymethyl-cellulose
- about 0.33% CMC is added to the bath and the glycerol concentration is preferably increased to about 4.8%.
- the application of CMC has the effect of partially drawing out water from the tubular body and thereby reducing its thickness. In the example here given, the thickness reduction is from the original 14 mils to about 10 mils.
- the hardened, plasticized and partially solidified tubular body is dried by hot air currents.
- the casing is inflated by blowing air into and through the length thereof as it passes into a drying chamber while at the some time warm air is blown over and around the exterior.
- This drying air is at approximately 80 C. and 8% relative humidity and the casing is subjected to such treatment until the wall thickness of the tubular body has been reduced to about 1 mil in the example under discussion.
- great care is taken during thisstep to prevent expansion or stretching of the air-inflated casing beyond the internal diameter imparted to it by the extrusion, e.g., 75 inch in the example given. mined by visual inspection, the dried casing tube being translucent, while the presence of moisture is indicated by a whitish, opaque color.
- an albumin powder may be blown into and through the inflated casing or otherwise applied, as more particularly described in United States Patent No. 3,123,480. Also after drying the dried tube may be partially re-humidified, by application of moist air, to avoid brittleness or cracking.
- the dried casing tube may then be subjected to automatic shirring and shirred lengths severed to form casings adapted to be stuffed on automatic stuffing machines.
- the casing is preferably subjected to a heat-curing treatment. This treatment comprises storage for about eight hours at a rising temperature brin ing the casing material from room temperature to about 80 C. It is then maintained at 80 C. fo some sixteen hours more, which completes the heat curing thereof.
- the achievement of suitable drying can be deterunease-e ti 6.
- drying said hardened body by passing it through a drying chamber and subjecting it therein to heated currents of air while maintaining the drying body in the form of a tube by inflation with air under pressure and controlling the pressure of said inflating air so as to maintain the inner diameter of the tube substantially the same as that at which it was extruded in the wet state.
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Description
United States Patent 3,194,365 ACHD DEPELATIGN AND EXTRUDABLE MERE. PRUDUCTKUN FRGM HHDE CGRIUM Paul V. Fagan, New iirnnswick, and Emanuel R. Lieberman, Somerville, NJ, assignors to .l'ohnson & Johnson, a corporation of New Jersey No Drawing. Fiied Oct. 1, 1962, Ser. No. 227,585 12 Claims. (Cl. Zed-409) The present invention relates to a method of treating hides and skins to prepare them for a subsequent conversion into a dispersion of swollen collagen fibrils for easing manufacture.
The collagen fibrils in bovine hides are arranged in bundles to form collagen fibers that vary in length and measure many thousand of Angstroms in diameter. Cowhide collagen fibers have been observed which measure about 10,000 to 20,000 Angstroms in diameter in the dehydrated state but larger collagen fibers measuring as much as 1,000 microns in diameter in their dehydrated state are believed to exist. Each collagen fiber contains hundreds or even thousands of fibrils, all bound together by a sheath. The collagen fibers in turn are organized into bundles of ollagen fibers that are large enough to be seen by the naked eye and form the familiar fibers visible in hides of all sorts. For all practical purposes, cowhide tissue is the commercially available raw material from which collagen fibrils can be obtained.
Edible sausage casings may be manufactured by extruding a mass of undegraded acid swollen collagen fibrils through an annular orifice to form a tubular casing which can then be treated in a manner to dehydrate and deswell the individual collagen fibril units. When the collagen fibrils in the extruded casing lose their excess water of hydration by air drying, they cohere to form a translucent hyaloid substance in which the boundary line between individual fibrils cannot be distinguished.
To make a dispersion of swollen collagen fibrils suitable for extrusion, the hide must first be freed from all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands. This upper portion of the hide has been aptly designatetd the thermostat layer by Wilson, since it contains those organs concerned with the regulation of body temperature. These structures are made up of proteins of the class known as keratin. The class of protein known as collagen, on the other hand, is present in that part of the hide lying beneath the thermostat layer, known as the corium. In trying to separate the keratin from the collagen without damage to the collagen, it is important to recognize the differences in properties between these two kinds of protein. Both keratin and collagen can be destroyed by strong solutions of acids or :alkalies, but acids destroy collagen more readily than they do keratin and alkalies destroy keratin more readily than they do collagen. For this reason, the separation has previously been eifected in alkaline solutions.
If a calf skin is immersed in a solution containing one pound of caustic soda per gallon of water, the hair will be quickly dissolved, but the true corium will not be irreparably damaged for leather manufacture until after the hair is gone. Nevertheless the method is a dangerous one even in the manufacture of leather because strong alkali will rapidly degrade collagen. The pH value of such a solution is about 14.0. At this pH value, collagen is hydrolyzed and destroyed although hair and epidermis are more quickly destroyed.
Centuries ago, tanners discovered that a solution of lime might be used to separate hair from skin without much damage to the skin. The reason for this is that lime has a limited saturability. If one pound of lime (calcium hydroxide) is put into a gallon of water, from 99.4 to 98.5 percent of it will remain undissolved because the solution becomes saturated at about 0.006 pound per gallon of water at boiling point and at about 0.015 pound per gallon of water near the freezing point. A saturated solution of lime has a pH value of about 12.5. It cannot be raised above this point by adding more lime because the excess will not dissolve.
Although lime treatment is quite suitable for leather manufacture, lime should not be used to dehair hides if the end product is to be an extruded casing. For although lime aids in the removal of hair and the epidermis layer, like most chemical reactions the liming of hides requires judgment and some compromise because the reaction of lime with keratin and collagen is not perfectly selective. The liming of hides is a very complicated reaction chemically which can effect the collagen fibrils that make up the hide in at least three ways:
(1) By deamidation and the minor destruction of the arginine residue resulting in an increase in free carboxylic groups.
(2) By breaking coordinate cross links between peptide bonds of adjacent peptide chains. This can result also in a greater up-take of cations, and
(3) Calcium hydroxide has a specific effect on collagen and a tendency to form complexes with hydroxy groups, which probably is connected with its low degree of ionization, its complexing power, and the bivalency of the cation.
The effects noted above may contribute to the inability of earlier Workers in this field to produce edible sausage casings using limed hides as a starting material.
It is an object of the present invention, therefore, to remove the hair, epidermis layer, thermostat layer and all keratin substances from fresh hides without denaturing or adversely effecting the collagen fibrils that make up the hide corium.
In accordance with the present invention, bovine hides are dehaired in such a way that the corium is not adversely affected for its subsequent use in the preparation of swollen collagen fibrils for casing manufacture. This may be accomplished by soaking the hide in a dilute aqueous solution of a weak acid that has a dissociation constant between l.O l0- and 1.0 10 in aqueous solutions. That one should in this manner be able to facilitate the removal of hair and epidermis without adversely effecting the collagen fibrils that make up the corium is all the more surprising in view of the known greater resistance of keratin to acid attack.
While the present invention is not to be limited by any particular theory, it is believed that the hairs are rendered removable from the skin by the dilute acid treatment because the acid swells and softens the corium of the skin, thus rendering the-hairs removable from the follicles and the epidermis removable from the collagencontaining derma. Inasmuch as the subsequent treatment of the corium to produce swollen collagen fibrils for casings involves further swelling with similar dilute solutions of weak acids, the unhairing of the hides with such acid solutions is not adverse to the subsequent treatment of the corium and in some cases may contribute favorably to such subsequent treatment.
Weak organic acids which may be used in the practice of the present invention are those having a dissociation is difficult to pass through the rollers of the splitting and dehairing machine. 7
The acidic aqueous solutions used may contain from 3 to 5% by weight of the organic acids described above, as required to give a pH of 2.3 to 3.7. At a pH above 3.7 it is necessary to treat the hides with the acid solution for a longer time and at a pH below 2.3 there is more danger of degrading the collagen. The acidic dehairing solution should be maintained at room temperature (about 7075 F.) and the fresh hides are permitted to soak in the acid bath with occasional agitation for 100 to 150 hours. The soaking'time in the bath may, of course, be reduced if the temperature of the bath is increased, but at elevated temperatures there will be some loss of the collagen due to acid hydrolysis and degradation.
The hides after this acid treatment are run through a defleshing machine and scraped on both sides to remove all hair epidermis and any adhering flesh. The cleaned corium so obtained is in a swollen condition because of Lsolvation that occurs during the acid treatment. This swelling interferes with cornminution and other mechanical handling of the skin during the preliminary stages of dispersing the collagen fibrils. It is necessary, therefore, after removal of the hair and epidermis to carefully neutralize and deswell the cleaned hide corium before proceeding further. During the neutralization step the cleaned hide corium is soaked in a weak aqueous alkaline bath at room temperature for about 12 hours. It is important to control the temperature and pH of the neutralizing bath to avoid alteration or degradation of the collagen. 'Moreover, the alkaline bath should not contain reagents, such as lime, or alkaline earth salts that might form an irreversible complex with the collagen. The alkaline bath may be prepared by dissolving ammonia or a soluble salt of a strong base and a weak acid, such as sodium bicarbonate, in water to give an alkaline pH below 10.0. Strongly alkaline agents must be avoided with regard to the ultimate use of the corium because the reagent used for neutralization and the ultimate pH of the neutralized skin are of. substantial importance as they effect the subsequent condition of the acid swollen collagen fibrils in the mass to be extruded.
Following the neutralization step the cleaned hide corium is Washed in Water for 3 to 4 hours. The hide corium after neutralization and washing is in a deswollen condition and may be subdivided, using conventional grinding equipment, to a particle size that is readily dispersible in dilute acid solution.'
It will be understood that the foregoing general descrip- 5 tion is exemplary and explanatory but does not restrict the invention. The process for dehairing fresh bovine hides may be more fully understood from the following description and example.
Forty steer hides, fresh from the slaughter house, are trimmed, fleshed, and placed in a drum bath with 3600 pounds of cold water (58 F). The hides are drummed for 30 minutes and the wash water is discarded. An aqueous acetic. acid solution is prepared in a paddle vat by adding to 3000 pounds of water at room temperature (70 F.) 111 pounds (3.7% by weight) of acetic acid. The washed steer hides are placed in the vat and the hides are agitated intermittently to insure that all sections of the hide surface contact the acidsolution. The pH of the acetic solution. increases from 3.2 to 3.5 after forty hours and the concentration of the acetic-acid in solution at this time is 3.3 by weight. Intermittent agitation is continued and at the end of'90 hours the acid concentration has diminished to 2.1% by weight and the pH is 3.7. The hides are allowed to soak in the vat for five days and five nights (120 hours) with occasional agitation to assure uniform treatment of all hides. After the acid treatment the hides are scraped on both sides to remove hair, epidermis and other undesirable matter.
The cleaned hide corium is then loaded into a large drum having a capacity for forty hides and carefully neutralized by washing for four hours at a temperature of 55410" F. in a dilute alkaline solution containing eighty pounds of sodium bicarbonate in 4,000 pounds of water. The total time required for neutralization in this alkaline wash is approximately 12 hours.
The neutralized hide corium is next washed in an overflow'bath for 3 to 4 hours in order to remove the salts formed during the neutralization step. The hide corium afte this final Wash is composed of substantially pure colagen fibrils free of all hair follicles and other extraneous matter. It may be comrninuted and reswollen in acid solution to form a homogeneous mass of swollen collagen fibrils useful in the manufacture of extruded collagen casings, as disclosed, for example, in United States Patents No. 3,123,653 and No. 3,123,482.
Composites are prepared from five hides; The hide composites are then cut into /2 to 4 square inch sections and reduced to pulp by three passes through a meat grinder, each pass being a finer grind. The first and second passes are through 18 and 8 millimeter holes, respectively. The final grind is through holes 1.5 millimeters in diameter. ltis important during the grinding process to keep the pulp below 20 C. This may be done by adding crushed ice to the hide sections as they are fed to the grinder.
The ground pulp is next diluted with tap water at 16 C. to give a smooth slurry containing 7.4% dry solids. This slurry parts) is then treated with 125 parts of a 2.4% lactic acid water solution using an inline mixer to form a homogeneous mass of swollen colagen fibrils. It is important during this acid swelling step also that the temperature be maintained below about 25 C. The mixture so obtained contains 3.7% hide solids and 1.2% lactic acid. After the pulp is blended with acid, the mass of swollen collagen fibrils is further dispersed in a suitable homogenizer, fitted with a 2-stage valve and operated with a 1500 p.s.i. drop per stage. In the ultimate fluid mass of swollen colagen fibrils so prepared the individual fibrils are freed from the fiber bundles and fibers and released from'the fiber sheaths. They take up all liquid and swell from an original diameter of the order of 300 A. to 1000 A. toa freshly swollen (one day old) maximum diameter of the order of 15,000 A.
Other mixtures prepared in similar manner may contain hide solids (in the above-described form of swollen collagen fibrils)'as low as about 3% and as high as about 5%, the preferred concentration of hide solids being about 4%. If the concentration is less than 2.5% the mixture is so watery that coagulation after extrusion becomes virtually impossible, while a concentration exceeding 6% requires very high extrusion pressures due to increased viscosity and tends to formation of tough casings. The preferred concentration of lactic acid is about 1.2% but may be as low as about 0.50%.
The fluid mass of swollen collagen fibrils obtained by the method above described is filtered through a 7-mil filter screen to remove unswollen collagen and noncolagenous materials, and then extruded in the form of a tube preferably in such away as to impart some collagen fibril orientation transverse to the extrusion direction. The particular design and operation of the extruder constitutes no essential part of the present invention, but it has been found preferable to utilize the action of the extruder to effect the maximum homogeneity of fibril distribution so as to impart substantial burst strength and transverse tear strength to the tube and ultimae casing while also eifectingorientation or alignment of fibrils or masses of fibrils in the direction of extrusion, particularly those adjacent the tube walls, thereby to achieve substantial longitudinal or tensile strength as well.
A preferred form of extruder utilizing the action of counter-rotating discs which facilitate a homogeneous and non-oriented distribution of fibrils, especially within the interior of the casing walls, is shown and described in United States Patent No. 3,122,788.
In accordance with the invention the extruded fluid mass of swollen collagen fibrils leaves the orifice of the extruder in the form of a tubular body of Watery fluid travelling preferably upwardly into a dehydrating or coagulating bath which surrounds the orifice of the extruder and extends upwardly therefrom. The initial coagulating bath into which the extruded tubular body immediately passes is preferably in the form of a vertical column of liquid constituting a housing surrounding and extending upwardly from the extruder orifice. A portion of this liquid flows upwardly within the extruded tubular body, passing between the extruded body and an internally disposed over-fiow or return tube. The flow rate within the extruded body is quite slow, to avoid pressures and velocities harmful to the delicate extruded body, and may be, e.g., about 1 gallon per hour. Another portion of the coagulating liquid flows upwardly in the housing outside the extruded tubular body and returns through an external overflow drain for recirculation. The fiow rate of said outside column of liquid may be relatively rapid, e.g., about 2 gallons per minute. Thus the inside and outside of the tubular body are initially bathed in upwardly flowing columns of a coagulating liquid.
It should be noted that the density of the extruded tubular body as it comes from the extruder orifice is substantially less than that of the coagulating salt solution into which it passes. Accordingly the tendency of the extruded tubular body is to rise and travel naturally upwardly in the coagulating liquid. This phenomenon facilitates the starting up of the extruder and the maintenance of the desired upward travel of the-tubular body with the exertion of a minimum of external forces thereupon. This action occurs at that stage in the treatment of the tubular body when it is weakest and most fragile and possesses virtually no integrity of its own.
After reaching the top of the liquid housing, the tubular body is passed into and through an extended bath of the coagulating liquid for a total coagulating exposure of about 6 minutes, although this time may be as short as about 3 minutes. The means and apparatus for accomplishing this transfer and subsequent conditioning operations will be hereinafter described in detail. This coagulating treatment is the first conditioning step applied afte extrusion of the tubular body. The extended coagulating bath itself is preferably an aqueous ammonium sulfate solution containing about 40% ammonium sulfate adjusted to a pH substantially higher than that of the acidswollen collagen material, e.g., a pH of about 7.0, with some suitable alkaline material such as sodium or ammonium hydroxide. The coagulating liquids in the vertical housing above the extruder and in said extended bath are of the same aforesaid composition. The purpose served by these coagulating baths is primarily to replace the water in the extruded tubular body by ammonium sulfate solution, thereby coagulating and giving temporary form and integrity to the tubular body so that it may be handled in the subsequent conditioning operations.
. The tubular body, when it passes from the extrusion nozzle or orifice, has a wall thickness determined by the annular space between the internal and external extruder tubes forming the orifice. In a preferred embodiment of the invention the external diameter of the inner extrusion tube is preferably about .75 while the radial distance between the exterior of said inner tube and the interior wall of the external tube is about .014". Thus the tubular body referred to will have an initial wall thickness of about .014" (14 mils) and this thickness will be substantially maintained throughout most of the liquid conditioning treatments as hereinafter described. Ultimately, in accordance with the invention, the dried tubular body will be reduced to a wall thickness of the order of .001" (1 mil), but the initial inne diameter of about .75 will be preserved. These dimensions are given by way of example and are not limiting, but to illustrate the relatively great reduction in wall thickness required and achieved by practice of the invention. The casing diameter of about .75" is typical of casings used for fresh pork sausages.
As a second conditioning step the concentration of coagulating salt in the coagulated tubular body is substantially reduced, thereby to facilitate the hardening action ereinafter described. In the preferred embodiment of the invention, hardening is effected by treatment with alum and it has been found that such treatment is effective only when the concentration of ammonium sulfate in the tubular body has been substantially reduced, yet a sufiicient amount thereof retained pro term to avoid undue softening and weakening of the coagulated tubular body. Accordingly the tubula body is pro-washed for a period of about six minutes in a much diluted water solution of ammonium sulfate (e.g., about 4% to 18%) similarly adjusted to pH of about 6.5.
In accordance with the invention, a third conditioning step constitutes a hardening of the coagulated casings by reaction of the collagen therein to alum. For this purpose the pre-washed coagulated tubular body is immersed in and treated with a solution containing, e.g., about 6% alum [NH Al(SO -24H O], 1% citric acid and 4% ammonium sulfate. The contact time is about six minutes and this alum hardening solution is maintained at pH 4.3.
This hardening treatment is sometimes called tanning, but the primary purpose is to efiect a hardening of the casing so as to make it resistant to water, which is not the case with collagen coagulated with ammonium sulfate. Without such hardening action the application of water to the tubular body coagulated with ammonium sulfate would reduce it to a formless gel. In other words the coagulation with ammonium sulfate is essentially a temporary step after which a more permanent hardening action is effected by treatment with alum. More detailed descriptions of the alum treatment with various examples thereof are given in United States Patent No. 3,123,481.
The fourth conditioning step, in accordance with the invention, involves removal of the ammonium sulfate salt which has remained in the tubular body after the pre-wash and alum hardening "steps. This excess am monium sulfate as well as any excess alum in the tubular body are removed by a prolonged washing of the tubular body in tap water, e.g., for about twenty minutes, preferably using two or more changes of water.
The fifth step in the conditioning of the tubular body is called a plasticizing operation. This procedure involves essentially two steps, one of which is the application of a humectant such as glycerine which preserves the softness of the material after drying and helps in rehumidifying it. This plasticizing material also prevents cracking and other effects consequent upon undue drying. As an example, the plasticizing bath may contain 3.6% glycerol, 20 parts per million formaldehyde and 0.1% sodium bicarbonate. The dwell time in this bath is about five minutes.
Concomitantly with the plasticizing step, carboxymethyl-cellulose (CMC) is preferably included in the plasticizing bath and applied thereby to the tubular body. For this purpose, about 0.33% CMC is added to the bath and the glycerol concentration is preferably increased to about 4.8%. A more detailed description of the composition of this combined plasticizing and CMC bath and variations thereof are given in United States Patent No. 3,123,483. The application of CMC has the effect of partially drawing out water from the tubular body and thereby reducing its thickness. In the example here given, the thickness reduction is from the original 14 mils to about 10 mils. Moreover, as described in United States Patent No. 3,123,483, the application of CMC improves the wet-strength of the casing before drying because of the proportionate increase in solid content. Moreover, it increases the burst-strength of the ultimate casing, thereby improving its properties during stufiing and cooking.
As the next or sixth conditioning step in the method, the hardened, plasticized and partially solidified tubular body is dried by hot air currents. For this purpose the casing is inflated by blowing air into and through the length thereof as it passes into a drying chamber while at the some time warm air is blown over and around the exterior. This drying air is at approximately 80 C. and 8% relative humidity and the casing is subjected to such treatment until the wall thickness of the tubular body has been reduced to about 1 mil in the example under discussion. In accordance with the invention, great care is taken during thisstep to prevent expansion or stretching of the air-inflated casing beyond the internal diameter imparted to it by the extrusion, e.g., 75 inch in the example given. mined by visual inspection, the dried casing tube being translucent, while the presence of moisture is indicated by a whitish, opaque color.
During the drying operation or immediately thereafter, an albumin powder may be blown into and through the inflated casing or otherwise applied, as more particularly described in United States Patent No. 3,123,480. Also after drying the dried tube may be partially re-humidified, by application of moist air, to avoid brittleness or cracking.
The dried casing tube may then be subjected to automatic shirring and shirred lengths severed to form casings adapted to be stuffed on automatic stuffing machines. As a final step, prior to stuffing but after shirring, the casing is preferably subjected to a heat-curing treatment. This treatment comprises storage for about eight hours at a rising temperature brin ing the casing material from room temperature to about 80 C. It is then maintained at 80 C. fo some sixteen hours more, which completes the heat curing thereof.
Other weak water soluble organic acids such as formic constant in'aqueous solution between 1.0 1O and LOX soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened; removing the hide from the acid solution and scraping the hide on both sides to remove from the hide corium all hair and flesh, the hair follicles epidermal layer, dermis and adnexial glands which consists of the sebaceous glands and sudorific glands; treating the dehaired and defieshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present and deswell the corium; washing the cleaned hide corium with water; comminuting the cleaned hide corium; and, reswelling the comminuted corium in acid solution to form a homogeneous mass of swollen collagen fibrils, all of the above steps being carried out at temperatures below C. 2. The process of claim 1 in which the aqueous acid solution is an acetic acid solution. I 3. The process of claim 1 in which the aqueous alkaline'solution is a solution of the salt of a strong base and a weak acid. 7
4. The process of claim 1 in which the aqueous acid solution is a lactic acid solution.
5. The process of claim 1 which the aqueous acid solution is a butyric acid solution. I
The achievement of suitable drying can be deterunease-e ti 6. The process of claim 1 in which the aqueous acid solution is a citric acid solution.
'7. The process of claim 1 in which the aqueous acid solution has a pH greater than 2.3 and less than 3.7.
8. .A process of producing swollen collagen fibrils for extrusion into edible sausage casings comprising the steps immersing fresh undehaired hide in a dilute aqueous solution of an acid having a dissociation constant in aqueous solution between l.() l()* and 1.0 10
Soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened;
Removing the hide from the acid solution and removing from the hide corium all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands;
Treating the dehaired and defieshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present and deswell the corium;
Comminuting the neutralized and deswelled corium,
and
Subjecting the comminuted corium to the swelling action of an aqueous solution of an acid having a dissociation constant between 1.0 10 and 1.O 10 whereby a mass of swollen collagen fibrils is obtained;
all of the above steps being carried out at temperatures below 25 C.
9. In the method of producing a tubular collagen casing, the steps of:
immersing fresh undehaired animal hide in a dilute aqueous solution of an acid having a dissociation constant in aqueous solution between 1.O 10 and soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened;
removing the hide from the acid solution and scraping the hide on both sides to remove from the hide corium all hair and flesh, the hair follicles, epidermal layendermis and adnexial glands which consist of the sebaceous glands and the sudorific glands,
treating the dehaired and defleshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present 7 and deswell the corium;
washing the cleaned, hide corium with water;
comminuting the cleaned hide corium and reswelling the comminuted corium in acid solution to form a homogeneous mass of swollen collagen fibrils;
extruding the homogeneous mass of swollen collagen fibrils to form a continuous, fragile tubular body; applying a coagulant to said tubular body; hardening the coagulated body;
washing coagulant from the hardened body;
maintaining substantially the same wall thickness in said tubular body throughout the aforesaid steps of coagulating, hardening and washing said body; and,
drying said body.
169. Ina method of producing collagen casings, the
steps of:
immersing fresh undehaired animal hide in a dilute aqueous solution of "an acid having a dissociation constant in aqueous solution between l.0 l0 and soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened;
removing the hide from the acid solution and scraping the hide on both sides to remove from the hide corium all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands;
treating the dehaired and defleshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present and deswell the corium;
washing the cleaned hide corium with water;
comminuting the cleaned hide corium and reswelling the cornminuted corium in acid solution to form a homogeneous mass of swollen collagen fibrils;
extruding the homogeneous mass of swollen collagen fibrils to form a continuous, fragile, tubular body;
applying a coagulant to said tubular body;
hardening said body in the wet state; and,
drying said hardened body by passing it through a drying chamber and subjecting it therein to heated currents of air while maintaining the drying body in the form of a tube by inflation with air under pressure and controlling the pressure of said inflating air so as to maintain the inner diameter of the tube substantially the same as that at which it was extruded in the wet state.
11. In the method of producing a tubular collagen casing, the steps of immersing fresh undehaired animal hide in a dilute aqueous solution of an acid having a dissociation constant in aqueous solution between 1.O 10 and l.0
soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened;
removing the hide from the acid solution and scraping the hide on both sides to remove from the hide corium all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands;
treating the dehaired and defieshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present and deswell the corium;
washing the cleaned hide corium with water;
comminuting the cleaned hide corium and reswelling the comminuted corium in acid solution to form a homogeneous mass of swollen collagen fibrils having a collagen solids content in the range of more than 2.5 and less than 6% by weight;
extruding the homogeneous mass of swollen collagen fibrils to form a continuous, fragile, tubular body;
applying a coagulant to said tubular body;
hardening the coagulated body;
washing coagulant from the hardened body;
maintaining substantially the same wall thickness in said tubular body throughout the aforesaid steps of coagulating, hardening and washing said body; and, drying said body,
while maintaining the internal diameter of said body substantially equal to that at which it is extruded.
1e 12. In the method of producing a tubular collagen casing, the steps of:
immersing fresh undehaired animal hide in a dilute aqueous solution of an acid having a dissociation constant in aqueous solution between 1.0 10- and soaking the hide in said acid solution until the epidermal layer and thermostat layer of said hide are swollen and softened;
removing the hide from the acid solution and scraping the hide on both sides to remove from the hide corium all hair and flesh, the hair follicles, epidermal layer, dermis and adnexial glands which consist of the sebaceous glands and the sudorific glands;
treating the dehaired and defieshed hide corium so obtained with a dilute aqueous alkaline solution to neutralize residual acid present and deswell the corium;
washing the cleaned hide corium with water;
comminuting the cleaned hide corium and reswelling the comrninuted corium in acid solution to form a homogeneous mass of swollen collagen fibrils having a collagen solids content in the range of more than 2.5% and less than 6% by weight;
extruding the homogeneous mass of swollen collagen fibrils to form a continuous, fragile, tubular body;
immersing said body in a solution of ammonium sulfate to coagulate the collagen therein;
immersing the coagulated body in an alum solution to harden the body and render it resistant to softening by water;
water washing the hardened body;
immersing the washed, hardened body in a plasticizing solution; and,
drying said body.
References Cited by the Examiner UNITED STATES PATENTS OTHER REFERENCES Marriott: J. Soc. Lea. Trades Chemists, 1921, pp. 2-9. Wilson: Chemistry of Leather Manufacture, 2nd ed.,
pp. 311-312, Vol. 1, 1928, pub. by The Chemical Catalog Co., Inc., N.Y.C.
NORMAN G. TORCHIN, Primary Examiner.
ABRAHAM H. WINKELSTEIN, Examiner.
Claims (1)
11. IN THE METHOD OF PRODUCING A TUBULAR COLLAGEN CASING, THE STEPS OF: IMMERSIING FRESH UNDEHAIRED ANIMAL HIDE IN A DILUTE AQUEOUS SOLUTION OF AN ACID HAVING A DISSOCIATIONL CONSTANT IN AQUEOUS SOLUTION BETWEEN 1.0X10**5 AND 1.0X10**-3; SOAKING THE HIDE IN SAID ACID SOLUTION UNTIL THE EPIDERMAL LAYER AND THERMOSTAT LAYER OF SAID HIDE ARE SWOLLEN AND SOFTENED; REMOVING THE HIDE FROM THE ACID SOLUTION AND SCRAPING THE HIDE ON BOTH SIDES TO REMOVE FROM THE HIDE CORIUM ALL HAIR AND FLESH, THE HAIR FOLICLES, EPIDERMAL LAYER, DERMIS AND ADNEXIAL GLANDS WHICH CONSIST OF THE SEBACEOUS GLANDS AND THE SUDORIFIC GLANDS; TREATING THE DEHAIRED AND DEFLESHED HIDE CORIUM SO OBTAINED WITH A DILUTE AQUEOUS ALKALINE SOLUTION TO NEUTRALIZE RESIDUAL ACID PRESENT AND DESWELL THE CORIUM; WASHING THE CLEANED HIDE CORIUM WITH WATER; COMMINUTING THE CLEANED HIDE CORIUM AND RESWELLING THE COMMINUTED CORIUM IN ACID SOLUTION TO FORM A HOMOGENEOUS MASS OF SWOLLEN COLLAGEN FIBRILS HAVING A COLLAGEN SOLIDS CONTENT IN THE RANGE OF MORE THAN 2.5% AND LESS THAN 6% BY WEIGHT; EXTRUDING THE HOMOGENEOUS MASS OF SWOLLEN COLLAGEN FIBRILS TO FORM A CONTINUOUS, FRAGILE, TUBULAR BODY; APPLYING A COAGULANT TO SAID TUBULAR BODY; HARDENING THE COAGULATED BODY; WASHING COAGULANT FROM THE HARDENED BODY; MAINTAINING SUBSTANTIALLY THE SAME WALL THICKNESS IN SAID TUBULAR BODY THROUGHOUT THE AFORESAID STEPS OF COAGULATING, HARDENING AND WASHING SAID BODY; AND, DRYING SAID BODY, WHILE MAINTAINING THE INTERNAL DIAMETER OF SAID BODY SUBSTANTIALLY EQUAL TO THAT AT WHICH IT IS EXTRUDED.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL298602D NL298602A (en) | 1962-10-01 | ||
GB1052872D GB1052872A (en) | 1962-10-01 | ||
BE638056D BE638056A (en) | 1962-10-01 | ||
US227585A US3194865A (en) | 1962-10-01 | 1962-10-01 | Acid depilation and extrudable fibril production from hide corium |
DE19631444997 DE1444997A1 (en) | 1962-10-01 | 1963-09-30 | Process for the production of swollen collagen fibrils suitable for sausage skin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US227585A US3194865A (en) | 1962-10-01 | 1962-10-01 | Acid depilation and extrudable fibril production from hide corium |
Publications (1)
Publication Number | Publication Date |
---|---|
US3194865A true US3194865A (en) | 1965-07-13 |
Family
ID=22853679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US227585A Expired - Lifetime US3194865A (en) | 1962-10-01 | 1962-10-01 | Acid depilation and extrudable fibril production from hide corium |
Country Status (5)
Country | Link |
---|---|
US (1) | US3194865A (en) |
BE (1) | BE638056A (en) |
DE (1) | DE1444997A1 (en) |
GB (1) | GB1052872A (en) |
NL (1) | NL298602A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3408918A (en) * | 1965-03-26 | 1968-11-05 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3425846A (en) * | 1965-07-13 | 1969-02-04 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3425847A (en) * | 1965-07-13 | 1969-02-04 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3508857A (en) * | 1966-02-25 | 1970-04-28 | Hoechst Ag | Process for removing keratin-containing parts from animal hides and pelts and the keratin-containing parts adhering to such hides and pelts |
US3525628A (en) * | 1967-11-20 | 1970-08-25 | Tee Pak Inc | Aluminum tannage of edible collagen casing |
US3534454A (en) * | 1969-02-07 | 1970-10-20 | Sato Hisao | Process of producing non-woven fabrics from modified collagen fibers |
US3620775A (en) * | 1968-08-12 | 1971-11-16 | Tee Pak Inc | Edible collagen casing |
US3894132A (en) * | 1973-09-10 | 1975-07-08 | Leonard Daniel | Method of forming collagen dispersions |
US3997290A (en) * | 1974-05-06 | 1976-12-14 | Del Cueto Eusebio | Process to separate and recover the solid and liquid phases from treatment baths of hides and skins |
US4814120A (en) * | 1984-02-21 | 1989-03-21 | Bioetica S.A. | Process for the preparation of collagen tubes |
JP2006513132A (en) * | 2002-05-21 | 2006-04-20 | コルテク オーストラリア リミテッド | Collagen and method for producing collagen |
US20130040885A1 (en) * | 2009-08-28 | 2013-02-14 | Tissue Science Laboratories Plc | Collagen pad |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2101877A (en) * | 1935-09-06 | 1937-12-14 | Eastman Kodak Co | Process for preparing photographic gelatin |
US2105036A (en) * | 1933-11-02 | 1938-01-11 | Firm Carl Freudenberg G M B H | Process for the manufacture of spun goods, fabrics, and other textiles |
US2485957A (en) * | 1946-04-26 | 1949-10-25 | American Cyanamid Co | Apparatus for treating strands |
US3123482A (en) * | 1961-01-16 | 1964-03-03 | R lieberman | |
US3123653A (en) * | 1960-09-20 | 1964-03-03 | Method of producing a tubular collagen casing |
-
0
- BE BE638056D patent/BE638056A/xx unknown
- GB GB1052872D patent/GB1052872A/en active Active
- NL NL298602D patent/NL298602A/xx unknown
-
1962
- 1962-10-01 US US227585A patent/US3194865A/en not_active Expired - Lifetime
-
1963
- 1963-09-30 DE DE19631444997 patent/DE1444997A1/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2105036A (en) * | 1933-11-02 | 1938-01-11 | Firm Carl Freudenberg G M B H | Process for the manufacture of spun goods, fabrics, and other textiles |
US2101877A (en) * | 1935-09-06 | 1937-12-14 | Eastman Kodak Co | Process for preparing photographic gelatin |
US2485957A (en) * | 1946-04-26 | 1949-10-25 | American Cyanamid Co | Apparatus for treating strands |
US3123653A (en) * | 1960-09-20 | 1964-03-03 | Method of producing a tubular collagen casing | |
US3123482A (en) * | 1961-01-16 | 1964-03-03 | R lieberman |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3408918A (en) * | 1965-03-26 | 1968-11-05 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3425846A (en) * | 1965-07-13 | 1969-02-04 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3425847A (en) * | 1965-07-13 | 1969-02-04 | Tee Pak Inc | Method of preparing an edible tubular collagen casing |
US3508857A (en) * | 1966-02-25 | 1970-04-28 | Hoechst Ag | Process for removing keratin-containing parts from animal hides and pelts and the keratin-containing parts adhering to such hides and pelts |
US3525628A (en) * | 1967-11-20 | 1970-08-25 | Tee Pak Inc | Aluminum tannage of edible collagen casing |
US3620775A (en) * | 1968-08-12 | 1971-11-16 | Tee Pak Inc | Edible collagen casing |
US3534454A (en) * | 1969-02-07 | 1970-10-20 | Sato Hisao | Process of producing non-woven fabrics from modified collagen fibers |
US3894132A (en) * | 1973-09-10 | 1975-07-08 | Leonard Daniel | Method of forming collagen dispersions |
US3997290A (en) * | 1974-05-06 | 1976-12-14 | Del Cueto Eusebio | Process to separate and recover the solid and liquid phases from treatment baths of hides and skins |
US4814120A (en) * | 1984-02-21 | 1989-03-21 | Bioetica S.A. | Process for the preparation of collagen tubes |
JP2006513132A (en) * | 2002-05-21 | 2006-04-20 | コルテク オーストラリア リミテッド | Collagen and method for producing collagen |
US20060149040A1 (en) * | 2002-05-21 | 2006-07-06 | John Snowden | Collagen and method for producing same |
US20130040885A1 (en) * | 2009-08-28 | 2013-02-14 | Tissue Science Laboratories Plc | Collagen pad |
Also Published As
Publication number | Publication date |
---|---|
DE1444997A1 (en) | 1969-02-06 |
GB1052872A (en) | |
BE638056A (en) | |
NL298602A (en) |
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