US3309165A - Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming - Google Patents
Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming Download PDFInfo
- Publication number
- US3309165A US3309165A US353631A US35363164A US3309165A US 3309165 A US3309165 A US 3309165A US 353631 A US353631 A US 353631A US 35363164 A US35363164 A US 35363164A US 3309165 A US3309165 A US 3309165A
- Authority
- US
- United States
- Prior art keywords
- resin
- tensile strength
- fabric
- cellulose
- textile
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 99
- 230000008569 process Effects 0.000 title claims description 78
- 229920005989 resin Polymers 0.000 title claims description 58
- 239000011347 resin Substances 0.000 title claims description 58
- 229920002678 cellulose Polymers 0.000 title claims description 32
- 239000001913 cellulose Substances 0.000 title claims description 32
- 239000004753 textile Substances 0.000 title claims description 32
- 230000006866 deterioration Effects 0.000 title claims description 13
- 230000002906 microbiologic effect Effects 0.000 title claims description 13
- 229920003180 amino resin Polymers 0.000 title claims description 9
- 238000010025 steaming Methods 0.000 title 1
- 239000000463 material Substances 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 4
- 230000002829 reductive effect Effects 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 230000003247 decreasing effect Effects 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 55
- 238000011282 treatment Methods 0.000 description 21
- 229920000742 Cotton Polymers 0.000 description 19
- 238000004132 cross linking Methods 0.000 description 15
- 238000001723 curing Methods 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 13
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000001035 drying Methods 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 6
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 6
- 238000009933 burial Methods 0.000 description 6
- 235000019253 formic acid Nutrition 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 5
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 238000013036 cure process Methods 0.000 description 5
- 244000005700 microbiome Species 0.000 description 5
- 241000006460 Cyana Species 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 230000002441 reversible effect Effects 0.000 description 4
- 241000272525 Anas platyrhynchos Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000013007 heat curing Methods 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 238000013508 migration Methods 0.000 description 3
- 230000005012 migration Effects 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 206010003549 asthenia Diseases 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 229920005565 cyclic polymer Polymers 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000001461 cytolytic effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000009988 textile finishing Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- ZHXAZZQXWJJBHA-UHFFFAOYSA-N triphenylbismuthane Chemical compound C1=CC=CC=C1[Bi](C=1C=CC=CC=1)C1=CC=CC=C1 ZHXAZZQXWJJBHA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
Definitions
- This invention relates to a procedure which Will reverse the tensile strength loss of cotton textiles normally associated with the use of condensation resins employed to render cellulosic fibers resistant to microbiological deterioration.
- condensation resins are also used to impart wash and wear properties in fabrics and the treatment procedure of this invention will also reverse the tensile strength loss that occurs in these treated fabrics.
- Resin treatment of cotton cloth to make it resistant to attack by microorganisms has a serious drawback, namely, a substantial loss in tensile strength of the treated material.
- This process essentially involves padding the scoured cotton fabric in a treatment solution containing 17% trimethylolmelamine, 20% formic acid and 63% water.
- the fabric which now has about an 80% wet pickup passes through a drying oven at 80 C. (176 F.) for 4 minutes, followed by curing at 140 C. (284 F.) for 4 minutes.
- Final resin deposition in the fabric for optimum resistance to microbial deterioration is about 12%.
- Fabric treated by this procedure undergoes 25-30% loss in tensile strength.
- blueline 8 02. cotton duck has a tensile strength of about 100 lbs. per square inch.
- the tensile strength of this fabric after treatment by Southern Regional process containing 11.8% resin addon becomes lowered to about 75 lbs. per square inch.
- the Arigal process can be carried on either semicontinuously by a wet-aging process at room temperature or at a slightly higher temperature or on a continuous basis using a conventional steamer.
- the main obstacle to processing on standard equipment by this process is the risk that the condensation-resin solution would migrate during Wet fixation. Measures taken to overcome this included the use of high rates of impregnation and higher concentrations of condensation-resin or the concentration of condensation-resin solution taken up by the fiber has to be increased by partial drying of the impregnated fabric.
- the catalyst and accelerator employed in this process are also different from the Ciba process, but the treated fabric presumably protects in a manner similar to the Ciba process; the resin is insolu-bilized within the fiber by the wet fixation process and the properties of the fabric are hardly changed.
- the tensile strength of the fabric in unaffected which is indicative of no crosslinking with the cellulose.
- the object of this invention is to provide a procedure which will reverse the loss of tensile strength associated with the conventional heat curing in the dry state of resin treatment procedures used to impart rot and weather resistance to cotton fabric.
- This invention is, therefore, a process for reversing the undesirable mechanical damage done to the physical properties of cotton fiber as a result of depositing condensation resins in the cotton fiber, and at the same time permitting retention of the desirable characteristic of resistance to microbiological deterioration.
- Ruperti Process for 7 days by Ruperti Process and dried at Prior art as taught by Rupertis wet fixation process might lead to the conclusion that emulsions of hardenable aminoplas-ts such as methylolrnelamine when applied to cellulosic fibrous material can be fixed to the fabric thereby rendering it resistant to microbiological deterioration wi'th no loss of tensile strength, but the Table above shows that this conclusion is not factual when applied to the Southern Regional process.
- blue-line fabric treated in a freshly prepared solution by the Southern Regional process except substituting Rupertis wet-cure process (curing the treated fabric in a plastic bag for 4 and 7 days at room tempera ture) for the drying (80 C.) and curing at C. resulted in the following: the blue-line fabric treated by this process did, in fact, retain its tensile strength while having a resin add-on of 12.5% and 12.9% respectively as monitored by nitrogen analysis determined after boiling the treated fabric for 30 minutes; this fabric, however, after 1-6 weeks burial retained only 37% and 11% of its tensile strength; however, drying the fabric at 80 C. (176 P.) (not to be confused with dry curing which is done at 140 C.
- Rupertis process called wet-fixing is a process whereby instead of hardening the aminoplast in the dry state, it can be converted into the insoluble state without previous drying and without completely removing the water derived from the impregnating solution so that a condensation product is formed in the wet state.
- Ruperti states that in the wet-fixing process the reaction takes a different course and the properties of the fiber are not changed in the way they are by dry heat hardening. Fundamental differences in the course of the reaction and the effects produced occur depending on whether dry hardening or wet fixing is used.
- the remaining six indicate possible modes of reaction with cellulose and include; (4) simple crosslink, (5) linear polymer, crosslinked to cellulose, (6) cyclic polymer, crosslinked to cellulose, -(7) monomer, linked to only one cellulose chain, (8) linear polymer, linked to only one cellulose chain, and (9) cyclic polymer, linked to only one cellulose chain.
- Rupertis and Cyana Sta-Tufi' finish process belong in one of the first three classes, and the Southern Regional process belongs to one of the latter six, probably by methylene groups crosslinking glucose units through ether formation.
- Ruperti is aimed to prevent crosslin-king at suggested temperatures of anywhere from room temperature to 80 C., noting that crosslinking will occur at higher temperatures which appears to suggest that such action should be avoided.
- the present process permits the crosslinking to take place with resultant loss in tensile strength, but reverses this by autoclaving, either at the time of manufacture or at a later date.
- This process is distinctly different than the Ruperti process where no crosslinking occurs and can be used with fast dry cure techniques where wet cure methods destroy the eifectivenesses of the dry cure treatment as shown in the Table.
- the fabric or yarn is padded as previously described and the material is dried uniformly with a minimum of resin migration. Once the resin is dried, it is fixed and is not removed to any appreciable mount by subsequent autoclaving. Thus, resin migration is prevented and there is no need to control the condensation of steam in this process.
- the time advantage is important in that the wet fixation process using steam under pressure requires thirty minutes exposure whereas the present procedure requires only a total of six to eight minutes, i.e., four to six minutes dry curing plus two minutes autoclaving. This represents a 70-80% savings in processing time, required to provide the desired end product and the time advantage is even greater if the wet cure process is used at room temperature where the curing is a matter of one to four days.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
United States Patent 3,309,165 PROCESS OF IMPROVING THE TENSILE STRENGTH AND INCREASING RESIST- ANCE TO MICROBIOLOGICAL DETE- RIORATION 0F CELLULOSE TEXTILE CONTAINING CURED AMINOPLAST RESIN BY STEAMTNG Morris R. Rogers, Framingham, and Arthur M. Kaplan,
Waban, Mass, assignors to the United States of America as represented by the Secretary of the Army No Drawing. Filed Mar. 20, 1964, Ser. No. 353,631 4 Claims. (Cl. 8-116.3)
The invention described herein may be manufactured and used by or for the Government for governmental purposes, without the payment to us of any royalty thereon.
This invention relates to a procedure which Will reverse the tensile strength loss of cotton textiles normally associated with the use of condensation resins employed to render cellulosic fibers resistant to microbiological deterioration.
It should be noted that condensation resins are also used to impart wash and wear properties in fabrics and the treatment procedure of this invention will also reverse the tensile strength loss that occurs in these treated fabrics.
One of the practical means of providing a durable, colorless, rot-resistant treatment to cotton is through the application of the acid colloid of trimethylolmelamine. Formic acid colloid of trimethylolmelamine is applied to fabric by essentially the same conventional method used for resin finishing, namely padding, drying and curing. This technique was developed at the Southern Regional Research Laboratory, USDA. and will hereafter be referred to as the Southern Regional process or SRRL.
It is well known that for many years that aminoplast resins applied by the conventional process to cotton will render it resistant to microbial attack. Acid colloids have been used by others but the techniques utilized produced stiff cotton goods with a variable degree of rot resistance.
Resin treatment of cotton cloth to make it resistant to attack by microorganisms, as practiced by the dry cure method exemplified by the Southern Regional process, has a serious drawback, namely, a substantial loss in tensile strength of the treated material. This process essentially involves padding the scoured cotton fabric in a treatment solution containing 17% trimethylolmelamine, 20% formic acid and 63% water. The fabric which now has about an 80% wet pickup passes through a drying oven at 80 C. (176 F.) for 4 minutes, followed by curing at 140 C. (284 F.) for 4 minutes. Final resin deposition in the fabric for optimum resistance to microbial deterioration is about 12%. Fabric treated by this procedure undergoes 25-30% loss in tensile strength. For example, blueline 8 02. cotton duck has a tensile strength of about 100 lbs. per square inch. The tensile strength of this fabric after treatment by Southern Regional process containing 11.8% resin addon becomes lowered to about 75 lbs. per square inch.
3,309,165 Patented Mar. 14, 1967 2 This loss in tensile strength is probably a result of crosslinking of the resin in association with the cellulose. Any loss in tensile strength of a fabric is considered undesirable and in practice may render the material too weak for certain end item use.
The Arigal process of Ciba Ltd. in conjunction with US. Patent No. 3,050,419 to A. Ruperti, claims to overcome the customary loss in tensile strength by depositing a synthetic resin in the fiber, this resin is not cured in the ordinary way, but fixed in the presence of water. The insolubilization of the resin within the fibers provides a permanent barrier against microorganisms. No reaction takes place with cellulose and the properties are hardly affected. The water absorption capacity of the fiber remains unchanged and its tensile strength remains unchanged.
The water present in the wet fixation hinders the crosslinking of the cellulose to such an extent that it hardly occurs in condensation-resin finishing. Some crosslinking can be obtained in wet fixation by working at higher temperatures or lengthening the reaction time. This would lead to the usual modification in the properties of the treated fabric and cause loss of strength. Crosslinking is not necessary for conversion, since insolubilized resin provides an adequate mechanical barrier against microorganism.
The Arigal process can be carried on either semicontinuously by a wet-aging process at room temperature or at a slightly higher temperature or on a continuous basis using a conventional steamer. The main obstacle to processing on standard equipment by this process is the risk that the condensation-resin solution would migrate during Wet fixation. Measures taken to overcome this included the use of high rates of impregnation and higher concentrations of condensation-resin or the concentration of condensation-resin solution taken up by the fiber has to be increased by partial drying of the impregnated fabric.
The following procedures for treatment of cotton fabric by the wet fixation process are recommended by A. Ruperti (American Dyestuff Reporter, vol. 50, pages 21- 24) in using the Arigal process:
(1) Continuous steam pr0cess.-The fabric is padded with a solution of Arigal (melamine-formaldehyde precondensate) to which hydrogen peroxide is added, and then squeezed and dried to a residual moisture of 20- 40%. The impregnated fabric is then steamed for at least eight minutes with saturated steam in a continuous ager. This procedure leads to the formation of formic acid by the oxidation of formaldehyde with hydrogen peroxide. The insolubilization of the resin within the fiber takes place rapidly.
(2) Semi-continuous wet aging-The fabric is impregnated with Arigal C and hydrogen peroxide, squeezed, and if necessary, dried to a residual moisture content of at least 20%. The fabric is then wrapped in plastic sheets to prevent drying. The rolls are kept either at room temperature, or slightly above, until the wet fixation process has been completed which usually required 1-4 days, depending on the temperature, 80 F.
3 (2427 C.) for at least 4 days or 24 hours at 105 F. (41 C).
(3) Formic acid process.Hydrogen peroxide is replaced by small amounts of formic acid which are not added to the impregnation bath but applied to the fabric after impregnation by spraying or nip-padding, etc. The resin is fixed Wet by one of the methods previously described. The Cyana Sta-Tutf Finish is also a resin treatment process using Aerotex Sta-Tutf Resin A and Areotex Sta-Tutf Accelerator B and curing by the wet fixation process at a convenient temperature. Although little information is made availableon the nature of the specific resin, it is presumed to be a fully methylated methylolmelamine. The catalyst and accelerator employed in this process are also different from the Ciba process, but the treated fabric presumably protects in a manner similar to the Ciba process; the resin is insolu-bilized within the fiber by the wet fixation process and the properties of the fabric are hardly changed. The tensile strength of the fabric in unaffected which is indicative of no crosslinking with the cellulose.
The object of this invention is to provide a procedure which will reverse the loss of tensile strength associated with the conventional heat curing in the dry state of resin treatment procedures used to impart rot and weather resistance to cotton fabric.
No established satisfactory procedure is known for reversing tensile strength loss associated with the dry heat cure resin treatment of cotton fabric. Rupertis procedure heretofore described states the use of his Wet fixation process does not permit any reaction to take place with the cellulose and the properties of the fabric are hardly affected. Thus, no crosslinking is effected and no loss in tensile strength takes place, which is in contrast to the curing of resins by dry heat. At elevated temperatures Ruperti, however, notes that crosslinking will occur.
However, with the Southern Regional process, areaction apparently does take place between the resin and the cellulose as evidenced by a loss in tensile strength after treatment, thus resulting in chemically modified cellulose. This reaction probably results in crosslinking between the cellulose chains; however as pointed out in Developments in Industrial Microbiology, 2, pages 79- 91 by W. N. Berard et al.; and in Textile Finishing Bulletin No. 136, American Cyanamid Co., Textile Resin Department by T. F. Cooke; resin finishes such as the acid colloid finish of the Southern Regional process do not act as a physical barrier to prevent microbiological attack as previously postulated but rather as a chemical barrier which renders cotton resistant to microbiological deterioration. The Arigal process, however, claims protection by providing an insoluble resin finish which acts as a mechanical barrier against microorganisms.
This invention is, therefore, a process for reversing the undesirable mechanical damage done to the physical properties of cotton fiber as a result of depositing condensation resins in the cotton fiber, and at the same time permitting retention of the desirable characteristic of resistance to microbiological deterioration.
The procedure for reversing the tensile strength loss in cotton fabric treated by the Southern Regional process as previously described in detail, consists in immediately thereafter or after an indefinite storage period, subjecting this treated fabric to steam under pressure (l6-18 lbs./ sq. in.) and at a temperature of 252-255 F. for a period of 2-20 minutes. This treatment leaves the mechanical properties of the fabric unchanged along with its resistance to microbiological deterioration. An 11.8% resin add-on to blue line 8 oz. duck gives the before and after soil burial tensile strength values as recorded in the following table.
TABLE [Average breaking strength in lbs. before and after soil burial note. Resin used in all treatments was Mousantos Resloom HP] Weeks Treatment on 8 oz. Blue Line Duck 0 riglnal 16 32 48 weeks weeks weeks 6. SRRL-T1eatment-Wet cured at room temp. for 4 days by Ruperti Process 7. SRRL-TreatxnentWet cured at room temp. for 4 days by Buperti Process and dried at 80 C 8. SRRL-Treatment-Wet cured at room temp. for 7 days by Ruperti Process SRRL-Treatment-Wet cured at room temp. for 7 days by Ruperti Process and dried at Prior art as taught by Rupertis wet fixation process might lead to the conclusion that emulsions of hardenable aminoplas-ts such as methylolrnelamine when applied to cellulosic fibrous material can be fixed to the fabric thereby rendering it resistant to microbiological deterioration wi'th no loss of tensile strength, but the Table above shows that this conclusion is not factual when applied to the Southern Regional process.
For example, blue-line fabric treated in a freshly prepared solution by the Southern Regional process except substituting Rupertis wet-cure process (curing the treated fabric in a plastic bag for 4 and 7 days at room tempera ture) for the drying (80 C.) and curing at C. resulted in the following: the blue-line fabric treated by this process did, in fact, retain its tensile strength while having a resin add-on of 12.5% and 12.9% respectively as monitored by nitrogen analysis determined after boiling the treated fabric for 30 minutes; this fabric, however, after 1-6 weeks burial retained only 37% and 11% of its tensile strength; however, drying the fabric at 80 C. (176 P.) (not to be confused with dry curing which is done at 140 C. (284 F.)) the fabric retained 86% and 56% of its tensile strength respectively after 16 weeks soil burial. Although wet curing applied to the SR=RL process did prevent loss in tensile, it certainly did not offer the protection in soil burial provided by the autoclaving treatment of this process.
The greater resistance of the wet cured blue-line fabric, as noted in the Table, followed by drying at 80 C. over the wet cured fabric 'is probably a result of a reaction between the resin and fabric noted in dry curing, although 80 C. is not usually considered a dry curing temperature.
The application of the wet fixation process of Ruperti to the SR-RL technique does not provide the degree of rot resistance to the Southern Regional process that might be expected. If the wet fixation process is followed, the degree of rot resistance is greatly reduced over that which is obtained by the Southern Regional process followed by autoclaving as disclosed in the above Table. Thus, this clearly indicates that the reaction between the resin and cellulose as controlled by the wet fixation process is a different chemical or physical phenomenon than exists between the cellulose and the resin undergoing a dry cure at elevated temperatures (140 C.) followed by autoclaving as described in the present process. This view is advanced as a rebuttal to a possible opinion that the application of this process to reverse the strength loss of the Southern Regional process is merely the application of the Ruperti or wet cure process at a different stage in the treatment procedure.
It should be noted that in order to form an insoluble condensation product within a fabric treated with an aminoplast resin by the conventional process such as the Southern Regional treatment, it is necessary to first dry the treated fabric and then subject the fabric to an elevated temperature such as 140 C. for approximately 4 minutes. By hardening in the dry state, water insoluble products are formed that cause a reduction in the tensile strength of the fabric.
By contrast, Rupertis process called wet-fixing, is a process whereby instead of hardening the aminoplast in the dry state, it can be converted into the insoluble state without previous drying and without completely removing the water derived from the impregnating solution so that a condensation product is formed in the wet state. Ruperti states that in the wet-fixing process the reaction takes a different course and the properties of the fiber are not changed in the way they are by dry heat hardening. Fundamental differences in the course of the reaction and the effects produced occur depending on whether dry hardening or wet fixing is used.
Reference is made to a publication in 1955 on Some Controversial Aspects of Crease Resistance of Cellulose Fabrics, Textile Research Journal 25 pages 24-40 by A. C. Nuessle et al. wherein is listed nine possible reactions when a difunctional resin-former is polymerized or cured within cellulose fibers. Three possible reactions involving only the resin polymerization and no bonding to cellulose can occur; (1) cyclic dimer, (2) linear polymer, and (3) thermoset polymer. The remaining six indicate possible modes of reaction with cellulose and include; (4) simple crosslink, (5) linear polymer, crosslinked to cellulose, (6) cyclic polymer, crosslinked to cellulose, -(7) monomer, linked to only one cellulose chain, (8) linear polymer, linked to only one cellulose chain, and (9) cyclic polymer, linked to only one cellulose chain.
It is assumed that Rupertis and Cyana Sta-Tufi' finish process belong in one of the first three classes, and the Southern Regional process belongs to one of the latter six, probably by methylene groups crosslinking glucose units through ether formation.
In Lineken et al. article in 195-6 entitled, Cellulose Interactions and Certain Textile Resins, it is pointed out that lowering of the tensile or breaking strength in cotton fabrics is an index of crosslinking. Since Rupertis process shows little or no loss in tensile strength, there is no reaction with cellulose, whereas the treatment of this process brings about a loss in tensile strength which is interpreted as indicative of crosslinking.
This leads to the conclusion that the Ruperti process and the SRRL process herein described are chemically different and therefore not synonymous in any way, other than that of providing two distinct methods for imparting rot and weather resistance to cotton fabric. Also the present process makes possible a dry cure process that has the advantage of a wet-cure process in eliminating tensile loss of treated fabric without the loss of the protective treatment against microbial attack.
It should be emphasized that the process of Ruperti is aimed to prevent crosslin-king at suggested temperatures of anywhere from room temperature to 80 C., noting that crosslinking will occur at higher temperatures which appears to suggest that such action should be avoided. The present process permits the crosslinking to take place with resultant loss in tensile strength, but reverses this by autoclaving, either at the time of manufacture or at a later date. This process is distinctly different than the Ruperti process where no crosslinking occurs and can be used with fast dry cure techniques where wet cure methods destroy the eifectivenesses of the dry cure treatment as shown in the Table.
Fabric treated by water soluble aminoplasts textile resins show excellent resistance to cellulolytic microorganisms, however none of them have resistance to noncellulolytic fungi. As a result, resin finished cotton will support the surface growth of mildew where the source of,
food is not the cotton fibers but rather from an external source such as oil, dirt or soil of some undetermined nature, and thus lower the aesthetic appearance of the fabric. I
Experiments show that resin treated cotton duck that has undergone autoclaving surprisingly shows greater resistance to surface growth than does the fabric treated by the'regular Southern Regional process. This is also an advantage over Rupertis process since it has been found necessary to add a fungicide to the fabric to prevent surface growth, although the Cyana Sta-Tuif finish claims to offer resistance to surface growing fungi.
In Rupertis process, as well as in the Sta-Tutf finish, care must be exercised to protect the fabric or yarn against water drops or splashes. During the wet fixation process when steam is used, condensed water is constantly being formed and must be removed by periodic opening of traps, but at the same time care must be exercised to prevent the excess loss of steam. The condensation of water on fabric or yarn in wet fixation will retard the fixation with the resulting migration of the resin. Also, if the material dries out locally or the material comes in contact with metal parts it will result in local drying which results in dry curing and a loss in tensile strength. This is also applicable to the Cyana Sta-Tuif finish.
This process circumvents these disadvantages. The fabric or yarn is padded as previously described and the material is dried uniformly with a minimum of resin migration. Once the resin is dried, it is fixed and is not removed to any appreciable mount by subsequent autoclaving. Thus, resin migration is prevented and there is no need to control the condensation of steam in this process.
The salient features of this process that are considered important are as follows:
(a) The treatment definitely reverses the tensile loss associated with the heat curing process as shown in the table above;
(b) Experiment shows that the fixation of the resin by the wet fixation is not more complete than the dry heat fixation followed by two minutes autoclaving;
(c) The durability of the conversion of the fabric is definitely proven in that this process conserves the fabric after aproximately one years soil burial as shown in the foregoing table;
((1) Tests also shown that the wet fixation process does not impart the degree of resistance as found by this process when applied to SRRL procedures.
(e) The time advantage is important in that the wet fixation process using steam under pressure requires thirty minutes exposure whereas the present procedure requires only a total of six to eight minutes, i.e., four to six minutes dry curing plus two minutes autoclaving. This represents a 70-80% savings in processing time, required to provide the desired end product and the time advantage is even greater if the wet cure process is used at room temperature where the curing is a matter of one to four days.
The treatment of this process and its accompanying ad vantages have been described in detail.
What is claimed is:
1. The process which comprises treating cellulose textile material with an aminoplast textile resin and an acidic catalyst, dry curing said textile resin on the textile material at high temperatures whereby the cellulose textile is cross-linked with said resin, the original tensile strength of the cellulose textile material is reduced and said resin cured textile is resistant to microbiological deterioration and weather; heating said resin cured textile material with steam at a temperature of about 252 to about 255 F. at a pressure of about 16 to 18 lbs. per sq. in. for a period of about 2 to 20 minutes whereby said resin cured textile has its original loss in tensile strength decreased and its resistance to loss of tensile strength through microbiological deterioration is further increased.
2. The process of claim 1 wherein said aminoplast textile resin is trimethylol melamine.
3. The process of claim 2 wherein said acidic catalyst is formic acid.
4. The process which comprises treating scoured cellulose textile material by padding it with a solution consisting of about 17% trimethylol melamine, about 20% acid catalyst and about 63% Water, passing said padded cellulose textile material through a dry oven at about 80 C., curing said dried textile material at about 140 C., Whereby the cellulose textile is cross-linked by the trirnethylol melamine, the original tensile strength of the cellulose textile material is reduced and said resin cured textile is resistant to microbiological deterioration and Weather;
References Cited by the Examiner UNITED STATES PATENTS 2,763,574 9/1956 Ruperti 8116.3 XR 3,050,419 8/ 1962 Ruperti 8116.3 X 3,119,715 1/1964 Reeves et a1. 8116.3 X
FOREIGN PATENTS 162,656 5/ 1955 Australia. 942,062 11/ 1963 Great Britain.
OTHER REFERENCES Decossas et al.: American Dyestuff Reporter, Aug. 21, 1961, pp. 33-35.
NORMAN G. TORCHIN, Primary Examiner.
H. WOLMAN, Assistant Examiner.
Claims (1)
1. THE PROCESS WHICH COMPRISES TREATING CELLULOSE TEXTILE MATERIAL WITH AN AMINOPLAST TEXTILE RESIN AND AN ACIDIC CATALYST, DRY CURING SAID TEXTILE RESIN ON THE TEXTILE MATERIAL AT HIGH TEMPERATURES WHEREBY THE CELLULOSE TEXTILE IS CROSS-LINKED WITH SAID RESIN, THE ORIGINAL TENSILE STRENGTH OF THE CELLULOSE TEXTILE MATERIAL IS REDUCED AND SAID RESIN CURED TEXTILE IS RESISTANT TO MICROBIOLOGICAL DETERIORATION AND WEATHER; HEATING SAID RESIN CURED TEXTILE MATERIAL WITH STEAM AT A TEMPERATURE OF ABOUT 252* TO ABOUT 255*F. AT A PRESSURE OF ABOUT 16 TO 18 LBS. PER SQ. IN. FOR A PERIOD OF ABOUT 2 TO 20 MINUTES WHEREBY SAID RESIN CURED TEXTILE HAS ITS ORIGINAL LOSS IN TENSILE STRENGTH DECREASED AND ITS RESISTANCE TO LOSS OF TENSILE STRENGTH THROUGH MICROBIOLOGICAL DETERIORATION IS FURTHER INCREASED.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US353631A US3309165A (en) | 1964-03-20 | 1964-03-20 | Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US353631A US3309165A (en) | 1964-03-20 | 1964-03-20 | Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming |
Publications (1)
Publication Number | Publication Date |
---|---|
US3309165A true US3309165A (en) | 1967-03-14 |
Family
ID=23389923
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US353631A Expired - Lifetime US3309165A (en) | 1964-03-20 | 1964-03-20 | Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming |
Country Status (1)
Country | Link |
---|---|
US (1) | US3309165A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3421923A (en) * | 1964-07-10 | 1969-01-14 | Ciba Ltd | Process for flame-proofing of cellulose-containing textiles |
US3528762A (en) * | 1965-05-10 | 1970-09-15 | Raduner & Co Ag | Process for abrasion resistant cellulose products |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763574A (en) * | 1951-07-10 | 1956-09-18 | Ciba Ltd | Method for protection of cellulosic fibrous material from attack by micro-organisms |
US3050419A (en) * | 1956-05-08 | 1962-08-21 | Ciba Ltd | Process for fixing aminoplasts in the wet state on cellulosic fibrous materials |
GB942062A (en) * | 1959-06-10 | 1963-11-20 | Courtaulds Ltd | Improvements in the finishing of cellulosic textile materials |
US3119715A (en) * | 1962-04-06 | 1964-01-28 | Wilson A Reeves | Processes for treating cellulosic textiles with acid colloids of methylolmelamine |
-
1964
- 1964-03-20 US US353631A patent/US3309165A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763574A (en) * | 1951-07-10 | 1956-09-18 | Ciba Ltd | Method for protection of cellulosic fibrous material from attack by micro-organisms |
US3050419A (en) * | 1956-05-08 | 1962-08-21 | Ciba Ltd | Process for fixing aminoplasts in the wet state on cellulosic fibrous materials |
GB942062A (en) * | 1959-06-10 | 1963-11-20 | Courtaulds Ltd | Improvements in the finishing of cellulosic textile materials |
US3119715A (en) * | 1962-04-06 | 1964-01-28 | Wilson A Reeves | Processes for treating cellulosic textiles with acid colloids of methylolmelamine |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3421923A (en) * | 1964-07-10 | 1969-01-14 | Ciba Ltd | Process for flame-proofing of cellulose-containing textiles |
US3528762A (en) * | 1965-05-10 | 1970-09-15 | Raduner & Co Ag | Process for abrasion resistant cellulose products |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4090844A (en) | Process of producing high performance durable-press cotton | |
US3666400A (en) | Sizing of yarns and fibers with combinations of polymers and crosslinking agents | |
US2436076A (en) | Method of stabilizing against shrinkage textile materials of regenerated cellulose | |
US2763574A (en) | Method for protection of cellulosic fibrous material from attack by micro-organisms | |
TR28229A (en) | Fabric treatment for reducing the fibrillation degree and fibrillation tendency of fabrics made from triangular fibers. | |
US3186954A (en) | Catalyst system for heat curing of fabrics | |
US3709657A (en) | Wet fixation of resins in fiber systems for durable press products | |
US3309165A (en) | Process of improving the tensile strength and increasing resistance to microbiological deterioration of cellulose textile containing cured aminoplast resin by steaming | |
US3768969A (en) | Sensitized textiles with decreased formaldehyde odor | |
US2504857A (en) | Art of imparting crease resistance to cotton fabrics | |
CA1036303A (en) | Flame retardant process for cellulosics | |
US3374107A (en) | Process for the treatment of textiles with aminoplasts | |
US3546006A (en) | Wet-fixation process for cellulosic fabrics using low add-ons of resins | |
US3926555A (en) | Modification of cotton textiles and cotton/polyester textile blends by photo-initiated polymerization of vinylic monomers | |
US4619668A (en) | Dyed wrinkle-resistant and durable-press cotton fabrics | |
US3402988A (en) | Chemical deactivation of catalyst at both faces of a cellulosic fabric impregnated with a resin-catalyst system to improve abrasion resistance of fabric after curing | |
US3100674A (en) | Process for shrink-proofing proteinaceous textile materials and the product therefrom | |
Lewin et al. | The role of liquid ammonia in functional textile finishes | |
US3119715A (en) | Processes for treating cellulosic textiles with acid colloids of methylolmelamine | |
US2925317A (en) | Shrinkproofing of protein fibers with polyalkyleneimines | |
US2622994A (en) | Method of producing linen-like effects on textiles | |
US3528762A (en) | Process for abrasion resistant cellulose products | |
US2485250A (en) | Treatment of wool and the like | |
US3926550A (en) | Cotton-tung oil durable-press textiles with high flex abrasion resistance | |
US3041199A (en) | Wrinkle resistant cellulose fabric and method of production |