US2842138A - Method for making bandage material for orthopedic casts and product thereof - Google Patents
Method for making bandage material for orthopedic casts and product thereof Download PDFInfo
- Publication number
- US2842138A US2842138A US405502A US40550254A US2842138A US 2842138 A US2842138 A US 2842138A US 405502 A US405502 A US 405502A US 40550254 A US40550254 A US 40550254A US 2842138 A US2842138 A US 2842138A
- Authority
- US
- United States
- Prior art keywords
- plaster
- paris
- resin
- bandage
- cast
- 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
- 239000000463 material Substances 0.000 title description 17
- 238000000034 method Methods 0.000 title description 15
- 230000000399 orthopedic effect Effects 0.000 title description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 75
- 239000011507 gypsum plaster Substances 0.000 claims description 73
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 claims description 72
- 239000000203 mixture Substances 0.000 claims description 18
- 230000003100 immobilizing effect Effects 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 229920005989 resin Polymers 0.000 description 62
- 239000011347 resin Substances 0.000 description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 20
- 238000001035 drying Methods 0.000 description 18
- 239000007788 liquid Substances 0.000 description 17
- 229920000877 Melamine resin Polymers 0.000 description 13
- 239000004744 fabric Substances 0.000 description 11
- 229910052602 gypsum Inorganic materials 0.000 description 11
- 239000010440 gypsum Substances 0.000 description 11
- 229920002689 polyvinyl acetate Polymers 0.000 description 8
- 239000011118 polyvinyl acetate Substances 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 6
- 239000011505 plaster Substances 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000010981 drying operation Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000005728 strengthening Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- IMTKRLUCQZWPRY-UHFFFAOYSA-N triazine-4-carbaldehyde Chemical compound O=CC1=CC=NN=N1 IMTKRLUCQZWPRY-UHFFFAOYSA-N 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 206010052428 Wound Diseases 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 150000004683 dihydrates Chemical class 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 206010021639 Incontinence Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/07—Stiffening bandages
- A61L15/08—Stiffening bandages containing inorganic materials, e.g. plaster of Paris
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/04—Plaster of Paris bandages; Other stiffening bandages
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/14—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00836—Uses not provided for elsewhere in C04B2111/00 for medical or dental applications
Definitions
- This invention relates to cast-forming elements designed to be used for immobilizing or supporting parts of the body.
- cast-forming elements composed of plaster of Paris or other settable material supported on suitable backing material are utilized in making casts that fit closely to the part of the body requir-
- the backing material is most usually in strip form wound into a roll or suitably pre-cut to the desired shape as, for instance, in manufacture of arm splints.
- the backing material may be woven gauze or crinoline of suitable mesh, or may be of knitted construction.
- the cast-forming element such as a bandage, may be immersed in water, excess water squeezed out by hand pressure, anclthe bandage then applied to the body in spiral fashion until enough thickness has been built up to provide the cast strength needed. 7
- plaster of Paris One technique of applying the plaster of Paris to the backing involves passing the backing fabric through a chamber in which the plaster of Paris, in the form of a fine powder, is dusted or otherwise coated on the backing. This is a dry operation, and the product is commonly known as looseplaster bandage.”
- the loose plaster bandage has marked disadvantages. The plaster is not firmly secured to the backing and'tends to drop off in'handling and wash oif during immersion of the bandage prior to application by the physician. This loss of plaster results in the production of casts of non-uniform and generally low strength.
- plaster of Paris bandages have always had certain inherent disadvantages which have long been well recognized by the profession and bythe trade. In'the first place, plaster of Paris has by nature a. high. density As! and is, therefore, a heavy material, which is a considerable disadvantage for ambulatory patients. Further, in order to assure adequate cast strength, it has been deemed advisable to employ plaster of Paris bandages in considerable thickness, which not only aggravates the weight disadvantage, but also decreases X-ray transparency. It would be desirable, if possible, to make a cast so thin that it would be permeable to X-rays, thereby making possible taking of X-ray pictures while the cast is still in place on the body of the patient.
- Set plaster of Paris casts are also notably susceptible to deterioration upon Contact with water. Improvement in water resistance would be of particular advantage in cases of incontinent patients, or in the case of arm casts which are apt to become wetted with water when the hands are being washed.
- Objects of the invention include improving the strength, lightness and X-ray transparency characteristics of plaster of Paris bandage casts. Another object is to incorporate a strengthening agent in hard-coated plaster of Paris bandages so as to improve the strength of the cast prepared therefrom. Still other objects comprise improving the early strength, resistance to deterioration from exposure to water after setting, and anti-microbial action of casts prepared from plaster of Paris bandages.
- the strength-giving material incorporated in the paste which is employed to impregnate the backing must, of course, be refractory to the retardant employed in cases where an aqueous liquid is utilized in the paste, and must in any case resist the elfect of the plaster of Paris itself. It must resist deterioration under conditions necessary to effect removal of liquid, i. e. elevated temperature.
- the finished bandage also must have stability so that it may be stored on the shelf of the wholesaler and retailer for a reasonable length of time without excessive decrease in strength-producing properties.
- a further object of the invention is to incorporate a strengthening agent in a hard-coated plaster of Paris bandage, the desired strengthening agent being refractory to the conditions to which it is subject, and the finished bandage having a suitable storage life.
- the foregoing objects are realized according to the invention in the form of a cast-producing element comprising a supporting fabric having bonded thereto a composition comprising 5 to 30% by weight of an aldehydetriazine resin, and -70% by weight of plaster of Paris based on the total weight of resin and plaster of Paris.
- the invention bandage is prepared by making a paste or slurry of a dispersing liquid, plaster of Paris and the.
- the triazine-aldehyde resin is preferably the one prepared from melamine, a species of triazines, with formaldehyde, a particular aldehyde.
- the condensation product of about 1 mol of melamine with about 3 or more mols of formaldehyde is suitable.
- the invention is not limited to a particular ratio of triazine to aldehyde, nor is it limited to a particular triazine, melamine, nor the particular aldehyde, formaldehyde.
- the triazine-aldehyde resin be water-dispersible, and be enpable of being cured to a hard-set water-insoluble state.
- the resins are of the type which are now commercially available, and which are described in United States Patent 2,260,239 issued October 21, 1941 to Talbott and United States Patent 2,310,004 issued February 2. 1943 to Widmer et al.
- a suitable resin may be made by mixing about 1 mol of melamine with 4 mols of formaldehyde in the form of a 37% aqueous solution (formalin).
- the formaldehyde is preferably first brought to a pH of 8.84 by addition of 3% aqueous solution of sodium hydroxide.
- the mixture of melamine and alkalinized formaldehyde is preferably heated under a reflux condenser for about 15 minutes, after which time water is removed overhead from the reaction vessel as the reaction proceeds. Removal of distillate is continued for about 15 minutes and until the temperature of the reactor charge is about 105 C. At this point the operation is interrupted and the batch cooled to about 60 C. as rapidly as possible.
- the product is a clear. slightly viscous oily-appearing syrup having a pH of about 8.1 and a resin content of about 50%. It may be used in preparing pastes of resin-plaster of Paris for impregnating fabrics to make plaster of Paris bandages according to the present invention.
- the plaster of Paris used for purposes of present invention may be ordinary plaster of Paris of the type conventionally incorporated in plaster of Paris bandages, or may be the high strength type plaster of Paris commonly known as alpha gypsum.
- alpha gypsum The latter material is disclosed and described in U. S. P. 1,901,051, issued March 14. 1933 to Randel and Dailey.
- This high strength gypsum is manufactured by calcination of gypsum rock in contact with steam at 17 to 20 lbs. gauge pressure. followed by drying and grinding.
- Alpha gypsum differs from ordinary plaster of Paris in that its compressive strength will range from 5000 lbs. per square inch on upward.
- Alpha ypsum is further differentiated from ordinary laster of Paris or hemihydrate in the physical nature of individual crystal fra ments composing the finely ground product. Tts properties and methods employed in production are fully disclosed in the above-mentioned Randel et al. patent.
- Triazine-aldehvde resin is incorporated in the paste or slurrv. and eventually in the completed plaster of Paris bandage. in amount sufiicient to impart to the final product a substantial increase in strength and substantial improvement in properties from the standpoints mentioned in the statement of objects above. Generally. appreciable improvement in properties may be noted if the amount of resin is at least about of the total combined weights of resin and plaster of Paris, i. e. 5% resin and 95% plaster of Paris. Optimum properties from the standpoint of final cast strength, early strength, resistance to water, etc., are noted within the preferred composition to resin, 90 to 85% plaster of Paris by weight. At resin compositions substantially above 15% advantages of the invention will still be notable.
- resin concentrations are generally maintained below about 30% by weight based on the combined weights of resin and plaster of Paris.
- the invention is not limited to a particular paste-forming liquid. Certain advantages of the invention inhere by use of organic nonaqueous liquids such as isopropyl alcohol, aqueous alcohol, or methylene chloride. In these cases, use of a retarder may be dispensed with since there is not sulficient water in the system to set the plaster of Paris in the slurry.
- the period between paste formation and the final drying of the bandage is a critical one in that the plaster of Paris and resin are subjected to conditions which tend to destroy or derogate from the soughtfor properties of the bandage.
- control of operating variables in this period is important.
- One yarrable to be controlled is the pH of the paste. pH 18 maintained above about 7.0, and preferably in the approximate range 7.0 to 10.0, in order to minimize curing of the triazinealdehyde resin. pH may be controlled by incorporat ng suitable amounts of alkalizing material and by ehmrnatmg any ingredients which would tend to lower the pH.
- Retarders other than the ammonium borate mentioned specifically may be employed providing they do not produce undesirably low pH so as to effect advancement or curing of the resin.
- Drying i. e. removal of liquid from the lmpr egnated bandage, whether it be aqueous or nonaqueous liquid as described above, is carried out at temperature and other conditions which minimize tendency of the resin to advance or cure. Removal of liquid should be brought about in the minimum time and at the minimum temperature feasible. That is, the drying conditions should be maintained so that the time required to effect desired degree of removal of liquid is short enough so that curing of the resin is not excessive. Furthermore, during this drying period temperature is maintained below a. level at which appreciable curing will take place, but sufiiciently high to efiect removal of water within the time limits specified above. Most preferably, temperatures are maintained at not greater than about 300 F. A suitable operating range of temperature for drying aqueous pastes may be found between 200 and 300 F.
- drying period liquid, particularly water, tends to promote or catalyze not only setting of the plaster of Paris, i. e. conversion to the dihydrate or gypsum, but also tends to catalyze advancement or curing of the resin.
- the resin once cured can impart no strengthening characteristics to the cast-forming bandage and, in fact, materially detracts from the strength properties that the plaster of Paris would have in the absence of any resin. Accordingly, drying conditions described above are maintained until free (volatile) water content of the bandage has been reduced to below 0.3% based on the weight of resin.
- the bandage is most preferably wrapped in a sealed sub stantially water vapor-impermeable wrapper or container promptly after leaving the drying operation. If the bandage material is to be slit into widths narrower than the web coated and dried in the bandage-making operation, such slitting will preferably be carried out after drying and before packaging so that the packaged bandage, once sealed, may be maintained intact until finally used by the consumer.
- Setting time of the bandage may be controlled by addition of accelerators or retarders known in the art to be eifective for controlling the setting time of the plaster of Paris.
- Retarders include soluble citrates, phosphates, acetates, or other organic retarders. These ingredients, when used, are generally incorporated into the plaster of Paris-resin paste described above.
- binders are polyvinyl acetate emulsions, described in U. S. P. 2,655,148.
- Other usable binders include emulsions or solutions of polymers of vinyl chloride, vinyl acetate, acrylates, methacrylates, or butadiene; or copolymers, interpolymers or polymeric mixtures thereof.
- the binder is preferably mixed into the paste just as are the other components of the bandage.
- the bandage is immersed in water according to the usual pro- Further, the resin in the bandage is optionally treated with a catalyst to' produce curing of the resin as rapidly as possible.
- This catalyst is conveniently added to the water in which the bandage is immersed.
- Catalyst concentrations in the water are maintained at a value sufiicient to produce in the resin the desired degree of cure in the desired interval of time. Catalyst concentrations of 0.5 to 6.0% may be found to produce the desired effect.
- One indicia of satisfactory environment for proper resin cure is pH, which is preferably maintained at about 6 or below in order toetfect proper resin cure within a short period of time at the relatively low temperature which will prevail.
- Acidity control may be produced by use of the resin-curing catalysts, for example ammonium'chloride or'. other acid salts 'or weak acids such as zinc sulfate, zinc chloride, aluminum sulfate, etc.
- Example I With parts of uncured water-soluble melamineformaldehyde resin prepared from a mixture of 1 mol melamine and 4 mols formaldehyde according to the foregoing procedure, there were mixed 90 parts of alpha gypsum prepared substantially according to the procedure of U. S. P. 1,901,051, and 40 parts water containing 0.5 part borax and 1.2 parts of polyvinyl acetate emulsion containing 55% polyvinyl acetate. The mixture had the consistency of a thin paste. It was coated on gauze and dried for about two minutes at 275 F.
- a strip of the dried bandage material 4 inches wide by 5 yards long was dipped into a l /2% aqueous solution of ammonium chloride and wrapped around a cylindrical member to prepare a cast.
- the cast was made of about 25 laminations of the gauze as measured through its thickness.
- the cast was allowed to set for 24 hours at room temperature after which time it was tested for cast strength according to Federal specification GG-B-l07, June 21, 1951, section 4.3.6 (except that setting time was 24 hours instead of 1 hour as called for by the specification). Strength tests were also made on similar casts after 7 days setting time. The result obtained is presented in the table below.
- Example II A homogeneous mixture was prepared of parts of melamine-formaldehyde resin substantially the same as that employed in Example I, 85 parts of alpha gypsum and 35 parts water containing 0.4 part boric acid, 0.8 parts 28% aqueous ammonia solution and 0.6 part polyvinyl acetate emulsion containing 55% polyvinyl acetate.
- Example III A paste similar to that described in Examples I and II was prepared using 25 parts aldehyde-triazine resin, 75 parts alpha gypsum and 45 parts water containing 0.6 part polyvinyl acetate emulsion, 0.4 part boric acid and 0.59 part of 28% aqueous ammonia. The mixture was coated on gauze and dried at 250 F. for about 3 minutes. A cast was prepared as in Example I and tested as described in that example. Results are presented in the table below.
- Example IV A paste similar to that described in the foregoing examples was prepared from parts alpha gypsum, 10 parts of the same resin and 50 parts of aqueous ethyl alcohol containing 1 part of polyvinyl acetate emulsion. The mixture was coated on ordinary gauze and dried at F. for 2 minutes. The cast was tested as in Example I, the results being presented in the table below.
- Example V The slurry in this example was composed of 85 parts alpha gypsum, 15 parts of the same resin and 2 parts of ammonium chloride, mixed with 60 parts of anhydrous methylene chloride containing 1 part of polyvinyl acetate emulsion. The mixture was spread on gauze using a knife coater, and dried at 100 F. for five minutes. A strip of the material 4 inches wide by 5 yards long was immersed in water, and a cast was prepared. The cast was tested according to the procedure described above with the results presented in the table below.
- the table also includes strength tests on a commercially available 4 inches wide by 5 yards long bandage made into a cast, the bandage being formed of alpha gypsum coated on and bonded to gauze, and having composition similar to invention bandages except that there was no aldehyde-triazine resin present.
- a bandage for producing an immobilizing cast comprising a fabric backing and bonded to said fabric a substantially dry composition comprising about 530% by weight of uncured aldehyde-triazine resin and about 95 70% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, and sufiicient adhesive to bond said composition to said backing.
- a bandage for producing an immobilizing cast comprising a fabric backing and bonded to said fabric a substantially dry composition comprising about 530% by weight of uncured melamine-formaldehyde resin and about 9570% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, and suflicient adhesive to bond said composition to said backing.
- a bandage for producing an immobilizing cast comprising a woven fabric backing and bonded to said fabric a substantially dry compositien comprising about 10 7 15% by weight of uncured melamine-formaldehyde resin and about 90-85% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, sufiicient adhesive to bond said composition to said backing, and plasticizer for said composition.
- the method of producing a plaster of Paris bandage which comprises preparing a paste of a liquid, plaster of Paris, and an uncured aldehyde-triazine resin, the amount of resin being about -30% and the amount of plaster of Paris being about 95-70% of the combined weights of resin and plaster of Paris, and sufficient adhesive to bond said resin and plaster of Paris to a Web, impregnating a web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin.
- the method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of a liquid, plaster of Paris, an uncured aldehyde-triazine resin, the amount of resin being about -15% and the amount of plaster of Paris being about 90-85% of the combined weights of resin and plaster of Paris, impregnating a fibrous web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin, and sealing the dried material in a substantially watcr-impervious Wrapper promptly after said drying operation.
- the method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, and retarder, the amount of resin being about 530% and the amount of plaster of Paris being about 95-70% of the combined weights of resin and plaster of Paris, impregnating a fibrous web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin.
- the method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, retarder and plasticizer, the amount of resin being about 10l5% and the amount of plaster of Paris being about -85% of the combined weights of resin and plaster of Paris, impregnating a woven fibrous web with said paste, drying the impregnated web at temperature not above 300 F. for time short enough and under conditions to prevent substantial curing of said resin, and controlling the pH of said bandage in the approximate range 7.0 to 10.0 during said drying operation.
- the method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, retarder and plasticizer, the amount of resin being about 10-15% and the amount of plaster of Paris being about 90-85% of the combined weights of resin and plaster of Paris, impregnating a woven fibrous web with said paste, drying the impregnated web at temperature not above 300 F. for time short enough to prevent substantial curing of said resin to volatile water content below about 0.3% based on the weight of said resin, controlling the pH of said bandage in the approximate range 7 to 10 during said drying operation, and sealing the dried material in a substantially waterimpervious wrapper promptly after said drying operation.
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Description
METHOD FOR MAKKNG ing immobilizing or support.
Unite ttes aten BANDAGE MATERIAL FOR ORTHOPEDIC CASTS AND PRUDUCT THEREGF No Drawing. Application January 21,
Serial No. 4055M;
8 Claims. (Cl. 128-431) This invention relates to cast-forming elements designed to be used for immobilizing or supporting parts of the body.
In conventional practice cast-forming elements composed of plaster of Paris or other settable material supported on suitable backing material are utilized in making casts that fit closely to the part of the body requir- The backing material is most usually in strip form wound into a roll or suitably pre-cut to the desired shape as, for instance, in manufacture of arm splints. The backing material may be woven gauze or crinoline of suitable mesh, or may be of knitted construction. In use, the cast-forming element, such as a bandage, may be immersed in water, excess water squeezed out by hand pressure, anclthe bandage then applied to the body in spiral fashion until enough thickness has been built up to provide the cast strength needed. 7
One technique of applying the plaster of Paris to the backing involves passing the backing fabric through a chamber in which the plaster of Paris, in the form of a fine powder, is dusted or otherwise coated on the backing. This is a dry operation, and the product is commonly known as looseplaster bandage." The loose plaster bandage has marked disadvantages. The plaster is not firmly secured to the backing and'tends to drop off in'handling and wash oif during immersion of the bandage prior to application by the physician. This loss of plaster results in the production of casts of non-uniform and generally low strength.
The patent faults of the loose plaster bandage gave rise to investigation into ways of improving adherence and minimizing loss of plaster of Paris from the backing material. The result of these developments was the hardcoated bandage in which the plaster of Paris is mixed with a liquid-dispersing medium into the paste or slurry, and this paste is' employed to impregnate the backing sheet. Upon drying of the plaste-impregnated backing one obtains a plaster of Paris bandage in which the plaster of Paris is bonded to the fabric, i. e. a hard-coated bandage. In procedures utilizing Water or aqueous liquids as dispersing medium for the paste it has been a problem to inhibit setting of the plaster of Paris, i. e. conversion of the hemihydrate to the dihydrate of calcium sulfate, between the time the paste is first prepared and the time the bandage is dried to produce the finished product. For this purpose, the use of'various retarders such as ammonium 'borate (disclosed in U. S. P; 2,557,083), or acetic acid has been proposed, or bandages have been prepared by the so-called -hot'water process in which setting of the plaster of Paris was prevented or minimized by keeping the paste hot during the critical period between initial wetting of the plaster and final drying of the bandage.
Plaster of Paris bandages have always had certain inherent disadvantages which have long been well recognized by the profession and bythe trade. In'the first place, plaster of Paris has by nature a. high. density As! and is, therefore, a heavy material, which is a considerable disadvantage for ambulatory patients. Further, in order to assure adequate cast strength, it has been deemed advisable to employ plaster of Paris bandages in considerable thickness, which not only aggravates the weight disadvantage, but also decreases X-ray transparency. It would be desirable, if possible, to make a cast so thin that it would be permeable to X-rays, thereby making possible taking of X-ray pictures while the cast is still in place on the body of the patient. Set plaster of Paris casts are also notably susceptible to deterioration upon Contact with water. Improvement in water resistance would be of particular advantage in cases of incontinent patients, or in the case of arm casts which are apt to become wetted with water when the hands are being washed.
Ordinary plaster of Paris bandages have no inherent resistance to growth or reproduction of microbes. Growth of micro-organisms between the skin and the cast, or within the cast itself, has in many cases created serious problems, particularly in cases of large body casts or body jackets which remain in place for weeks or even months. Growth of micro-organisms within the cast may be even more serious in cases where casts are placed over open wounds or points of irritation. Hence, it would be desirable, if feasible, to prepare a cast which possesses inherent anti-microbial properties so as to eliminate or minimize the tendency of microbes to live and reproduce within the cast.
Objects of the invention include improving the strength, lightness and X-ray transparency characteristics of plaster of Paris bandage casts. Another object is to incorporate a strengthening agent in hard-coated plaster of Paris bandages so as to improve the strength of the cast prepared therefrom. Still other objects comprise improving the early strength, resistance to deterioration from exposure to water after setting, and anti-microbial action of casts prepared from plaster of Paris bandages.
The strength-giving material incorporated in the paste which is employed to impregnate the backing must, of course, be refractory to the retardant employed in cases where an aqueous liquid is utilized in the paste, and must in any case resist the elfect of the plaster of Paris itself. It must resist deterioration under conditions necessary to effect removal of liquid, i. e. elevated temperature.
The finished bandage also must have stability so that it may be stored on the shelf of the wholesaler and retailer for a reasonable length of time without excessive decrease in strength-producing properties. A further object of the invention, therefore, is to incorporate a strengthening agent in a hard-coated plaster of Paris bandage, the desired strengthening agent being refractory to the conditions to which it is subject, and the finished bandage having a suitable storage life.
The foregoing objects are realized according to the invention in the form of a cast-producing element comprising a supporting fabric having bonded thereto a composition comprising 5 to 30% by weight of an aldehydetriazine resin, and -70% by weight of plaster of Paris based on the total weight of resin and plaster of Paris. The invention bandage is prepared by making a paste or slurry of a dispersing liquid, plaster of Paris and the. uncured aldehyde-triazine resin, plus a suitable amount of retarder if required, the amount of resin and plaster of Paris being in the ranges aforesaid, impregnating the backing with'the paste, and drying the impregnated backing in a time short enough to prevent substantial curing of the resin and at a temperature high enough to effect drying of the bandage within the time requirement, but below temperature at which substantial curing of the resin would take place. Advantageous properties of the invention bandage include greater cast strength (including superior early strength), resistance to water after setting of 3. the cast, resistance to micro-organisms, and other advantages suggested by the foregoing recitation of objects. Other features of the invention and its preferred embodiments are set forth hereinafter.
The triazine-aldehyde resin, the use of which is contemplated according to the present invention, is preferably the one prepared from melamine, a species of triazines, with formaldehyde, a particular aldehyde. The condensation product of about 1 mol of melamine with about 3 or more mols of formaldehyde is suitable. However. the invention is not limited to a particular ratio of triazine to aldehyde, nor is it limited to a particular triazine, melamine, nor the particular aldehyde, formaldehyde. It is, however, preferred according to the invention that the triazine-aldehyde resin be water-dispersible, and be enpable of being cured to a hard-set water-insoluble state. The resins are of the type which are now commercially available, and which are described in United States Patent 2,260,239 issued October 21, 1941 to Talbott and United States Patent 2,310,004 issued February 2. 1943 to Widmer et al. Alternatively, a suitable resin may be made by mixing about 1 mol of melamine with 4 mols of formaldehyde in the form of a 37% aqueous solution (formalin). The formaldehyde is preferably first brought to a pH of 8.84 by addition of 3% aqueous solution of sodium hydroxide. The mixture of melamine and alkalinized formaldehyde is preferably heated under a reflux condenser for about 15 minutes, after which time water is removed overhead from the reaction vessel as the reaction proceeds. Removal of distillate is continued for about 15 minutes and until the temperature of the reactor charge is about 105 C. At this point the operation is interrupted and the batch cooled to about 60 C. as rapidly as possible. The product is a clear. slightly viscous oily-appearing syrup having a pH of about 8.1 and a resin content of about 50%. It may be used in preparing pastes of resin-plaster of Paris for impregnating fabrics to make plaster of Paris bandages according to the present invention.
The plaster of Paris used for purposes of present invention may be ordinary plaster of Paris of the type conventionally incorporated in plaster of Paris bandages, or may be the high strength type plaster of Paris commonly known as alpha gypsum. The latter material is disclosed and described in U. S. P. 1,901,051, issued March 14. 1933 to Randel and Dailey. This high strength gypsum is manufactured by calcination of gypsum rock in contact with steam at 17 to 20 lbs. gauge pressure. followed by drying and grinding. Alpha gypsum differs from ordinary plaster of Paris in that its compressive strength will range from 5000 lbs. per square inch on upward. Alpha ypsum is further differentiated from ordinary laster of Paris or hemihydrate in the physical nature of individual crystal fra ments composing the finely ground product. Tts properties and methods employed in production are fully disclosed in the above-mentioned Randel et al. patent.
Triazine-aldehvde resin is incorporated in the paste or slurrv. and eventually in the completed plaster of Paris bandage. in amount sufiicient to impart to the final product a substantial increase in strength and substantial improvement in properties from the standpoints mentioned in the statement of objects above. Generally. appreciable improvement in properties may be noted if the amount of resin is at least about of the total combined weights of resin and plaster of Paris, i. e. 5% resin and 95% plaster of Paris. Optimum properties from the standpoint of final cast strength, early strength, resistance to water, etc., are noted within the preferred composition to resin, 90 to 85% plaster of Paris by weight. At resin compositions substantially above 15% advantages of the invention will still be notable. However, as resin concentration increases above this value there may be a corresponding increase in difiiculty of preparing and impregnating the paste on the backing fabric, and particularly where aqueous pastes are utilized there may be increased difiiculty in removing water from the impregnated fabric to produce the desired dry finished bandage. Accordingly, resin concentrations are generally maintained below about 30% by weight based on the combined weights of resin and plaster of Paris.
From the standpoint of simplicity of operation and required apparatus it is preferable to employ water as liquid dispersant for the paste or slurry. However, the invention is not limited to a particular paste-forming liquid. Certain advantages of the invention inhere by use of organic nonaqueous liquids such as isopropyl alcohol, aqueous alcohol, or methylene chloride. In these cases, use of a retarder may be dispensed with since there is not sulficient water in the system to set the plaster of Paris in the slurry.
As indicated above, the period between paste formation and the final drying of the bandage is a critical one in that the plaster of Paris and resin are subjected to conditions which tend to destroy or derogate from the soughtfor properties of the bandage. Hence, control of operating variables in this period is important. One yarrable to be controlled is the pH of the paste. pH 18 maintained above about 7.0, and preferably in the approximate range 7.0 to 10.0, in order to minimize curing of the triazinealdehyde resin. pH may be controlled by incorporat ng suitable amounts of alkalizing material and by ehmrnatmg any ingredients which would tend to lower the pH. Retarders other than the ammonium borate mentioned specifically may be employed providing they do not produce undesirably low pH so as to effect advancement or curing of the resin.
Drying, i. e. removal of liquid from the lmpr egnated bandage, whether it be aqueous or nonaqueous liquid as described above, is carried out at temperature and other conditions which minimize tendency of the resin to advance or cure. Removal of liquid should be brought about in the minimum time and at the minimum temperature feasible. That is, the drying conditions should be maintained so that the time required to effect desired degree of removal of liquid is short enough so that curing of the resin is not excessive. Furthermore, during this drying period temperature is maintained below a. level at which appreciable curing will take place, but sufiiciently high to efiect removal of water within the time limits specified above. Most preferably, temperatures are maintained at not greater than about 300 F. A suitable operating range of temperature for drying aqueous pastes may be found between 200 and 300 F.
The reason for the critical nature of the drying period is that liquid, particularly water, tends to promote or catalyze not only setting of the plaster of Paris, i. e. conversion to the dihydrate or gypsum, but also tends to catalyze advancement or curing of the resin. The resin once cured, of course, can impart no strengthening characteristics to the cast-forming bandage and, in fact, materially detracts from the strength properties that the plaster of Paris would have in the absence of any resin. Accordingly, drying conditions described above are maintained until free (volatile) water content of the bandage has been reduced to below 0.3% based on the weight of resin. Pursuant to maintaining desired low water content of the bandage and preventing the bandage, once dried, from absorbing water from the atmosphere, the bandage is most preferably wrapped in a sealed sub stantially water vapor-impermeable wrapper or container promptly after leaving the drying operation. If the bandage material is to be slit into widths narrower than the web coated and dried in the bandage-making operation, such slitting will preferably be carried out after drying and before packaging so that the packaged bandage, once sealed, may be maintained intact until finally used by the consumer.
The resinplaster of Paris bandages of the invention cedure.
may contain conventional amounts "of'plasticizer such as glycerols, glycols, polyglycols, etc. Setting time of the bandage may be controlled by addition of accelerators or retarders known in the art to be eifective for controlling the setting time of the plaster of Paris. Retarders include soluble citrates, phosphates, acetates, or other organic retarders. These ingredients, when used, are generally incorporated into the plaster of Paris-resin paste described above.
Another ingredient employed in preferred embodiments of the invention is a binder which serves the purpose of elfecting maximum adhesion of the plaster of Paris and resin to the bandage backing material. Suitable binders are polyvinyl acetate emulsions, described in U. S. P. 2,655,148. Other usable binders include emulsions or solutions of polymers of vinyl chloride, vinyl acetate, acrylates, methacrylates, or butadiene; or copolymers, interpolymers or polymeric mixtures thereof. The binder is preferably mixed into the paste just as are the other components of the bandage.
To produce a cast of the invention bandage, the bandage is immersed in water according to the usual pro- Further, the resin in the bandage is optionally treated with a catalyst to' produce curing of the resin as rapidly as possible. This catalyst is conveniently added to the water in which the bandage is immersed. Catalyst concentrations in the water are maintained at a value sufiicient to produce in the resin the desired degree of cure in the desired interval of time. Catalyst concentrations of 0.5 to 6.0% may be found to produce the desired effect. One indicia of satisfactory environment for proper resin cure is pH, which is preferably maintained at about 6 or below in order toetfect proper resin cure within a short period of time at the relatively low temperature which will prevail. ,Acidity control may be produced by use of the resin-curing catalysts, for example ammonium'chloride or'. other acid salts 'or weak acids such as zinc sulfate, zinc chloride, aluminum sulfate, etc.
The following examples, in which parts are on a weight basis unless otherwise specifically indicated, are presented not in a limiting sense but as illustrating the invention.
Example I With parts of uncured water-soluble melamineformaldehyde resin prepared from a mixture of 1 mol melamine and 4 mols formaldehyde according to the foregoing procedure, there were mixed 90 parts of alpha gypsum prepared substantially according to the procedure of U. S. P. 1,901,051, and 40 parts water containing 0.5 part borax and 1.2 parts of polyvinyl acetate emulsion containing 55% polyvinyl acetate. The mixture had the consistency of a thin paste. It was coated on gauze and dried for about two minutes at 275 F. A strip of the dried bandage material 4 inches wide by 5 yards long was dipped into a l /2% aqueous solution of ammonium chloride and wrapped around a cylindrical member to prepare a cast. The cast was made of about 25 laminations of the gauze as measured through its thickness. The cast was allowed to set for 24 hours at room temperature after which time it was tested for cast strength according to Federal specification GG-B-l07, June 21, 1951, section 4.3.6 (except that setting time was 24 hours instead of 1 hour as called for by the specification). Strength tests were also made on similar casts after 7 days setting time. The result obtained is presented in the table below.
Example II A homogeneous mixture was prepared of parts of melamine-formaldehyde resin substantially the same as that employed in Example I, 85 parts of alpha gypsum and 35 parts water containing 0.4 part boric acid, 0.8 parts 28% aqueous ammonia solution and 0.6 part polyvinyl acetate emulsion containing 55% polyvinyl acetate.
I The paste was coated on gauze backing and dried. After preparing a cast according to the procedure described in Example I, strength tests were carried out as described above. The results of tests for east strength are presented in the table below.
Example III A paste similar to that described in Examples I and II was prepared using 25 parts aldehyde-triazine resin, 75 parts alpha gypsum and 45 parts water containing 0.6 part polyvinyl acetate emulsion, 0.4 part boric acid and 0.59 part of 28% aqueous ammonia. The mixture was coated on gauze and dried at 250 F. for about 3 minutes. A cast was prepared as in Example I and tested as described in that example. Results are presented in the table below.
Example IV A paste similar to that described in the foregoing examples was prepared from parts alpha gypsum, 10 parts of the same resin and 50 parts of aqueous ethyl alcohol containing 1 part of polyvinyl acetate emulsion. The mixture was coated on ordinary gauze and dried at F. for 2 minutes. The cast was tested as in Example I, the results being presented in the table below.
Example V The slurry in this example was composed of 85 parts alpha gypsum, 15 parts of the same resin and 2 parts of ammonium chloride, mixed with 60 parts of anhydrous methylene chloride containing 1 part of polyvinyl acetate emulsion. The mixture was spread on gauze using a knife coater, and dried at 100 F. for five minutes. A strip of the material 4 inches wide by 5 yards long was immersed in water, and a cast was prepared. The cast was tested according to the procedure described above with the results presented in the table below. For purpose of comparison the table also includes strength tests on a commercially available 4 inches wide by 5 yards long bandage made into a cast, the bandage being formed of alpha gypsum coated on and bonded to gauze, and having composition similar to invention bandages except that there was no aldehyde-triazine resin present.
Cast Strength Pounds Example After 1 After 7 Day Days The invention is not limited to the foregoing examples and description since there are many modifications and equivalents within the scope of the invention.
The claims are:
1. A bandage for producing an immobilizing cast comprising a fabric backing and bonded to said fabric a substantially dry composition comprising about 530% by weight of uncured aldehyde-triazine resin and about 95 70% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, and sufiicient adhesive to bond said composition to said backing.
2. A bandage for producing an immobilizing cast comprising a fabric backing and bonded to said fabric a substantially dry composition comprising about 530% by weight of uncured melamine-formaldehyde resin and about 9570% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, and suflicient adhesive to bond said composition to said backing.
3. A bandage for producing an immobilizing cast comprising a woven fabric backing and bonded to said fabric a substantially dry compositien comprising about 10 7 15% by weight of uncured melamine-formaldehyde resin and about 90-85% by weight of plaster of Paris based on the total weight of resin and plaster of Paris, sufiicient adhesive to bond said composition to said backing, and plasticizer for said composition.
4. The method of producing a plaster of Paris bandage which comprises preparing a paste of a liquid, plaster of Paris, and an uncured aldehyde-triazine resin, the amount of resin being about -30% and the amount of plaster of Paris being about 95-70% of the combined weights of resin and plaster of Paris, and sufficient adhesive to bond said resin and plaster of Paris to a Web, impregnating a web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin.
5. The method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of a liquid, plaster of Paris, an uncured aldehyde-triazine resin, the amount of resin being about -15% and the amount of plaster of Paris being about 90-85% of the combined weights of resin and plaster of Paris, impregnating a fibrous web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin, and sealing the dried material in a substantially watcr-impervious Wrapper promptly after said drying operation.
6. The method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, and retarder, the amount of resin being about 530% and the amount of plaster of Paris being about 95-70% of the combined weights of resin and plaster of Paris, impregnating a fibrous web with said paste, and drying the impregnated web under conditions to prevent substantial hydration of said plaster of Paris and to prevent substantial curing of said resin.
7. The method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, retarder and plasticizer, the amount of resin being about 10l5% and the amount of plaster of Paris being about -85% of the combined weights of resin and plaster of Paris, impregnating a woven fibrous web with said paste, drying the impregnated web at temperature not above 300 F. for time short enough and under conditions to prevent substantial curing of said resin, and controlling the pH of said bandage in the approximate range 7.0 to 10.0 during said drying operation.
8. The method of claim 4 for producing a plaster of Paris bandage which comprises preparing a paste of an aqueous liquid, plaster of Paris, an uncured melamineformaldehyde resin, retarder and plasticizer, the amount of resin being about 10-15% and the amount of plaster of Paris being about 90-85% of the combined weights of resin and plaster of Paris, impregnating a woven fibrous web with said paste, drying the impregnated web at temperature not above 300 F. for time short enough to prevent substantial curing of said resin to volatile water content below about 0.3% based on the weight of said resin, controlling the pH of said bandage in the approximate range 7 to 10 during said drying operation, and sealing the dried material in a substantially waterimpervious wrapper promptly after said drying operation.
References Cited in the file of this patent UNITED STATES PATENTS 2,419,440 Delmonte Apr. 22, 1947 2,557,083 Eberl June 19, 1951 2,571,343 Dailey Oct. 16, 1951 OTHER REFERENCES The Lancet for Dec. 19, 1953, pp. 1317-18.
Claims (1)
1. A BANDAGE FOR PRODUCING AN IMMOBILIZING CAST COMPRISING A FABRIC BACKING AND BONDED TO SAID FABRIC A SUBSTANTIALLY DRY COMPOSITION COMPRISING ABOUT 5-30% BY WEIGHT OF UNCURED ALDEHYDE-TRIAZINE RESIN AND ABOUT 9570% BY WEIGHT OF PLASTER OF PARIS BASED ON THE TOTAL WEIGHT OF RESIN AND PLASTER OF PARIS, AND SUFFICIENT ADHESIVE TO BOND SAID COMPOSITION TO SAID BACKING.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US405502A US2842138A (en) | 1954-01-21 | 1954-01-21 | Method for making bandage material for orthopedic casts and product thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US405502A US2842138A (en) | 1954-01-21 | 1954-01-21 | Method for making bandage material for orthopedic casts and product thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2842138A true US2842138A (en) | 1958-07-08 |
Family
ID=23603962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US405502A Expired - Lifetime US2842138A (en) | 1954-01-21 | 1954-01-21 | Method for making bandage material for orthopedic casts and product thereof |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2842138A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3236232A (en) * | 1962-11-20 | 1966-02-22 | David F Smith | Adhesive for bonded plaster of paris products |
| US3282265A (en) * | 1965-02-10 | 1966-11-01 | David F Smith | Plaster of paris product and process improvements |
| US3284227A (en) * | 1962-12-06 | 1966-11-08 | Fibreboard Paper Products Corp | Catalyzed gypsum wallboard and method of production thereof |
| US3508626A (en) * | 1967-12-22 | 1970-04-28 | Franklin Robbins | Acoustic diaphragm |
| US4214578A (en) * | 1977-11-18 | 1980-07-29 | Johnson & Johnson | Orthopedic bandage having improved conformability |
| US5609680A (en) * | 1992-12-21 | 1997-03-11 | Maeta Concrete Industry Ltd. | Cement, cement products, molding material, a concrete member and a method of producing the same |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419440A (en) * | 1947-04-22 | |||
| US2557083A (en) * | 1947-07-22 | 1951-06-19 | Johnson & Johnson | Plaster bandage and method and composition for making same |
| US2571343A (en) * | 1945-01-25 | 1951-10-16 | United States Gypsum Co | Self-setting plastic material consisting essentially of alpha-gypsum and an aminotriazine resin |
-
1954
- 1954-01-21 US US405502A patent/US2842138A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419440A (en) * | 1947-04-22 | |||
| US2571343A (en) * | 1945-01-25 | 1951-10-16 | United States Gypsum Co | Self-setting plastic material consisting essentially of alpha-gypsum and an aminotriazine resin |
| US2557083A (en) * | 1947-07-22 | 1951-06-19 | Johnson & Johnson | Plaster bandage and method and composition for making same |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3236232A (en) * | 1962-11-20 | 1966-02-22 | David F Smith | Adhesive for bonded plaster of paris products |
| US3284227A (en) * | 1962-12-06 | 1966-11-08 | Fibreboard Paper Products Corp | Catalyzed gypsum wallboard and method of production thereof |
| US3282265A (en) * | 1965-02-10 | 1966-11-01 | David F Smith | Plaster of paris product and process improvements |
| US3508626A (en) * | 1967-12-22 | 1970-04-28 | Franklin Robbins | Acoustic diaphragm |
| US4214578A (en) * | 1977-11-18 | 1980-07-29 | Johnson & Johnson | Orthopedic bandage having improved conformability |
| US5609680A (en) * | 1992-12-21 | 1997-03-11 | Maeta Concrete Industry Ltd. | Cement, cement products, molding material, a concrete member and a method of producing the same |
| US5614009A (en) * | 1992-12-21 | 1997-03-25 | Maeta Concrete Industry Ltd. | Cement, cement products, molding material, a concrete member and a method of producing the same |
| US5651816A (en) * | 1992-12-21 | 1997-07-29 | Maeta Concrete Industry Ltd. | Cement, cement products, molding material, concrete member and a method of producing the same |
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