US2092749A - Process and composition of matter - Google Patents

Process and composition of matter Download PDF

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US2092749A
US2092749A US637559A US63755932A US2092749A US 2092749 A US2092749 A US 2092749A US 637559 A US637559 A US 637559A US 63755932 A US63755932 A US 63755932A US 2092749 A US2092749 A US 2092749A
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acid
cloth
tensile strength
water
nitrated
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US637559A
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George B Bradshaw
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EIDP Inc
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EI Du Pont de Nemours and Co
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/58Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides
    • D06M11/64Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides with nitrogen oxides; with oxyacids of nitrogen or their salts

Definitions

  • This invention relates to acid resistant material, particularly fibers and fabrics which are capable of withstanding the chemical action of mineral acids, and a process for the manufacture 5 thereof. It especially contemplates the production of filter-cloths which are not only highly acid resistant but possess excellent mechanical strength.
  • Example I Unbleached loosely woven cotton cloth formed of loosely spun threads and containing about 3% to 9% of moisture was produced without subjecting the cotton to artificialheat or otherwise treating it in any manner so as to cause deterio- More specifically, the fabric referred to-was a carded Chafer Peeler, 9% ounce per square yard weight, 30 pick warp, 30 pick filler, threads 20-4 ply and square weave. A piece of this material was immersed in eighty times its own weight of a mixed acid solution containing about 83% nitric acid,11% sulfuric acid, and 6% water, the temperature being maintained r at about 20 C. to 25 C.
  • the treatment was continued for about 30 minutes (or until the maximum nitrogen content possible without loss of tensile strength had been obtained).
  • the cloth was then removed from the first acid bath and quickly submerged in a body of practically anhy- 20 drous mixed acid containing about 50% nitric acid and 50% sulfuric acid.
  • the volume of acid and temperature employed were substantially the same as for the first acid.
  • This second treatment was continued for about one hour.
  • the cloth 25 was then removed from the second acid bath and washed. It contained by analysis about 13.4% nitrogen on the dry basis.
  • Example II A piece of 21 ounce per square yard weight loosely woven twill, thefibers of which had never been deteriorated by boiling or otherwise, was treated by the procedure set out in Example I.
  • Example III other than the usual process of fumigating Egyptian cotton upon its arrival in the United States, was treated as described in Example I. The most desirable results were obtained with a 20 minute treatment in the first acid and a 40 minute treatment in the second acid. The tensile strength of the nitrated cloth was substantially the same as that of the unnitrated cloth.
  • the process of the invention is preferably applied to materials of the class known as pcto celluloses (cotton, ramie, flax, hemp and the like) as distinguished from the ligno celluloses (wood and the like).
  • the nitration may cause it to shrink from 15% to in area and, for this reason, it is desirable to use a loosely woven material. Furthermore, a tightly woven fabric does not allow the acid to penetrate satisfactorily. The best results are generally obtained when the warp and woof of the fabric are equl-distant and have substantially the same tensile strength.
  • the cellulosic fiber or fabric to be nitrated it is preferable that such conditioning be effected without ever removing therefrom substantial amounts of the natural moisture, that is, the moisture which remains in the cellulose fiber when it is allowed to air-dry under normal atmospheric conditions.
  • the water content may vary from about 3% to 12% by weight of the various cellulose materials and, for any particular kind of cellulose, may vary on either side of the average water content by about 1% to 2% by weight within the extreme range ofv ordinary atmospheric conditions.
  • the composition of the nitrating acid may vary widely. It should preferably be so regulated as to eifect nitration of the fiber or fabric without substantial gelatinization. At the same time, the concentration of nitric acid present should preferably be sumciently high to insure penetration of the fiber or fabric. If nitrating acid of relatively high l-lNOa contentis/ not used initially,
  • the reaction with the cellulose, which forms water, may dilute the acid to such an extent that the cellulosic fibers are not uniformly nitrated.
  • sulfuric acid used in the nitrating acid, it is desirable that it be present in relatively small amounts, since the formation of cellulose sulfate esters which would. occur to a considerable extent if large proportions of sulfuric acid were present has the effect of weakening the fibers undesirably.
  • a relatively small amount of sulfuric acid may increase the penetrating power of the nitric acid without weakening the fiber substantially.
  • the nitrating acid may contain other reagents adapted to increase the penetrating pbwer of the nitric acid, as for example, acetic acid or phosphoric acid.
  • nitrating acids which may be used in this stage may be mentioned anhydrous nitric acid, nitric acid containing water, or a nitric acid-sulfuric acid solution which may contain water. If a nitric acid-water solution is employed, the amount of water present should preferably be less than about 4% by weight. In general, it is preferable to employ a mixed nitric-sulfuric acid solution having an HNQa content of at least about 76% by weight, the remainder being sulfuric acid and/or water (preferably not exceeding 12%).
  • composition of the acid solution employed for the second treatment may also. vary within relatively wide limits. It is preferable, however, that the water content of this second acid should vary from about 4% to nightly fuming.
  • the acid content of this second solution should preferably be more than about and less than about 60% EH03, the remainder being H2SO4. Especially desirable results are obtained when the first acid solution contains about 82% to 83% EH03, 7% to 8% H20 and about 10% H2804, and the second acid solution contains about to HNOa and 45% to 50% H2804. Small amounts of mo; may also be present in the acid solutions employed.
  • each acid bath should preferably be such that the heat of reaction is'quickly dissipated and that the strength of the acid is maintained nearly uniform in spite of the water formed from the reaction with the cellulose.
  • the temperaturesof the acid baths should preferably be not lower than about 12 C. or higher than about 30 C.
  • the reaction slows up to an undesirable extent when temperatures much lower than 20 C. are utilized and a slowing up of the reaction is particularly disadvantageous for the reason that time is allowed for side reactions.
  • the temperature utilized exceeds about 30 C., reactions may occur which weaken the fiber or fabric.
  • the cellulosic fiber may have its nitrogen content raised to about 13% in the first treatment,
  • the method of nitration may be varied widely. It may conveniently'be a so-called pot process in which the nitrating acids are contained in open vessels. The cloth is then immersed in the first acid by suspending it from rods and weighting it at the bottom. After the desired nitration is effected, it is removed from the first acid and transferred to the second acid. In the transfer some of the first acid is carried along. After immersion in the second acid, it may be withdrawn and washed with a stream of water. The finished cloth is preferably preserved in a damp or wet state.
  • nitrated fabrics produced in accordance with the preferred process of this invention are more resistant to acids than a y of the types of filter-cloths previously known. They are particularly advantageous for use in filter press filtrations because in such operations it is desirable that the filter cloth used should possess not only good mechanical strength and resistance to acids but also pliability to the extent that the cloth will return to its original shape when the filter cake has been removed. In a given filter press filtration involving an acidic solution, the improved filter cloths prepared according to the'present invention will last at least seventy times longer than the same cloth unnitrated.
  • a process of producing nitrated cellulosic materials highly resistant to acids the steps which comprise treating cellulose materials with a nitrating acid sufficiently high in nitric acid and deficient in water and auxiliary penetrating acid, and at a temperature and for a time such that partial nitration is effected without substantially changing the appearance of the material treated and without substantially altering its tensile strength, and continuing the nitration with a more strongly nitrating acid which contains less nitric acid, about 0'4% water and materially more auxiliary penetrating acid than the first acid, until the nitrogen content of the material treated is in excess of 13%.
  • nitrated cellulosic materials highly resistant to acids the step which comprises nitrating a cellulose material to a nitrogen content in excess of 13% with a nitrating acid containing about 40% to about 60% HNOs,
  • the process of producing acid resistant materials which comprises subjecting an undeteriorated cotton fabric to the action of an acid solution containing at least 76% HNOS, not more than 12% water, the remainder being H2504, until the maximum nitrogen content of the product is obtained without substantial loss of tensile strength and thereafter treating the resultant product with a nitric-sulfuric acid solution containing less than about 4% water, and more than about 40% HNOz but less than about 60% HNOs, until the nitrogen content of said product is about 13.4% by weight, while maintaining a ternperature of 20 C. to 30 C. in both acid solutions.
  • a nitrated natural cellulosic fabric containing about 13.4% nitrogen characterized by the properties that it possesses at least 85% of the tensile strength of the original unnitrated fabric for the same linear Width and retains at least 50% of its tensile strength after being immersed in %0% sulfuric acid for thirty minutes at 90 C.
  • a nitrated natural cotton fabric containing about 13.4% nitrogen characterized by the properties that it possesses at least 85% of the tensile strength of the original unnitrated fabric for the same linear width and retains at least 50% of its tensile strength after being immersed in 40% sulfuric acid for thirty minutes at 90 C.

Description

Patented Sept. 14, 1937 UNITED SAT TENT 2,092,749 rRocEss AND coMPosrrion or MATTER No Drawing.
This invention relates to acid resistant material, particularly fibers and fabrics which are capable of withstanding the chemical action of mineral acids, and a process for the manufacture 5 thereof. It especially contemplates the production of filter-cloths which are not only highly acid resistant but possess excellent mechanical strength.
As is well known, it is impossible to filter solid materials from an acid medium with ordinary filter cloth, for the reason that the cloth is destroyed by the action of the acid. It is known also that when cloth of cellulosic origin is subjected to the action of nitric acid there results a change in the cloth which makes it less susceptible to the action of mineral acids such as, for example, hydrochloric, sulfuric, phosphoric and nitric acids. Heretofore, this increase in resistance to acids has always been accompanied by a lowering of the tensile strength of the cloth to the extent that it was of little commercial value. Furthermore, the treatment of the cloth with nitric acid caused it to become harder, more or less brittle, and somewhat gelatinized.
I It is an object of the present invention to produce fibers and fabrics, and especially filter cloths,
which are highly acid resistant, are pliable, and
possess good tensile strength. A further object is the provision of a new and improved process for producing materials of the character above described. Other objects of the invention will be. apparent by reference to the following de scripticn thereof.
These objects are accomplished according to 30 the invention whereby highly acid-resistant materials are obtained by treating certain cellulosic fibers and/or fabrics with a ni-trating acid to produce a product containing. in excess of 13.0%,
and preferably about 13.4% nitrogen by weight, while regulating the concentration of the acid, the temperature and the time of treatment to avoid substantial gelatinization of the cellulose and substantial loss of tensile strength. The 45 process of nitration is preferably effected'by subecting the cellulosic materials to the action of nitric acid in stages. p I I While the invention is susceptible of considerable variation and modification in the manner of 50 its practical application, particularly as regards the nature and proportions of the materials and the exact procedure employed, the following examples will illustrate how the invention may be practiced. The proportions and concentrations 55 are given by weight.
, ration of the cellulose.
application Uctober 12, 1932, Serial No. 637,559
10 Claims. (Cl. Mil-204i) Example I Unbleached loosely woven cotton cloth formed of loosely spun threads and containing about 3% to 9% of moisture was produced without subjecting the cotton to artificialheat or otherwise treating it in any manner so as to cause deterio- More specifically, the fabric referred to-was a carded Chafer Peeler, 9% ounce per square yard weight, 30 pick warp, 30 pick filler, threads 20-4 ply and square weave. A piece of this material was immersed in eighty times its own weight of a mixed acid solution containing about 83% nitric acid,11% sulfuric acid, and 6% water, the temperature being maintained r at about 20 C. to 25 C. The treatment was continued for about 30 minutes (or until the maximum nitrogen content possible without loss of tensile strength had been obtained). The cloth was then removed from the first acid bath and quickly submerged in a body of practically anhy- 20 drous mixed acid containing about 50% nitric acid and 50% sulfuric acid. The volume of acid and temperature employed were substantially the same as for the first acid. This second treatment was continued for about one hour. The cloth 25 was then removed from the second acid bath and washed. It contained by analysis about 13.4% nitrogen on the dry basis. Samples of the original cloth and the nitrated cloth were tested for tensile strength, and it was found that for the same 30 linear width of sample, the tensile strength of the nitrated cloth was substantially the same as that of the ail-nitrated 010th.
' Example II A piece of 21 ounce per square yard weight loosely woven twill, thefibers of which had never been deteriorated by boiling or otherwise, was treated by the procedure set out in Example I.
It was found desirable to continue the treatment 40 in the first acid for about one and one-half hours and the treatment in the second acid for about three hours. The tensile strength of the nitrated cloth was. about 85% of that of the unnitrated cloth for the same linear length. It was noted,
however, that the shrinkage of this heavier cloth was not as much as that of the lighter weight cloth described in'Example I.
Example III other than the usual process of fumigating Egyptian cotton upon its arrival in the United States, was treated as described in Example I. The most desirable results were obtained with a 20 minute treatment in the first acid and a 40 minute treatment in the second acid. The tensile strength of the nitrated cloth was substantially the same as that of the unnitrated cloth.
All of the cloths described in the examples were tested by immersion in 40% sulfuric acid for thirty minutes at 90 -C., and it was found that all of the cloths retained at least 50% of their tensile strength. It will be recognized that these testing conditions are rather severe and are I not such as are likely to be encountered in orany weight. In general, the relatively heavy fabrics such as described in Example II have been found to be most desirable for filter press operations. While the most highly advantageous results have been obtained in the treatment of cotton fabrics, in its broader aspects the invention contemplates the treatment of certain other cellulosic materials. It has been found that linen, for example, may also be treated with very satisfactory results. In general, the process of the invention is preferably applied to materials of the class known as pcto celluloses (cotton, ramie, flax, hemp and the like) as distinguished from the ligno celluloses (wood and the like).
When cloth is nitrated as herein described, the nitration may cause it to shrink from 15% to in area and, for this reason, it is desirable to use a loosely woven material. Furthermore, a tightly woven fabric does not allow the acid to penetrate satisfactorily. The best results are generally obtained when the warp and woof of the fabric are equl-distant and have substantially the same tensile strength.
In the practice of the invention, it has been found that the results obtained in nitrating natural cellulosic materials of the class described are far superior to those obtained in the nitration of materials which have been chemically treated. Thus, it was found that when a cotton twill comparable to that used in Example 11 was boiled in a weak alkaline solution (about 2% soda ash based on the weight of the cloth) for six to eight hourawashed until neutral and dried at 105 C. to constant weight, then nitramd as in Example H, the nitrated cloth obtained had a much lower tensile strength than the cloth of Example T1 and was of little value for commercial filter-press operations. Since it is customary in the manufacture of cellulosic fabrics to heat, bleach, or otherwise chemically treat them, thediscovery that natural fibers and fabrics yield better results is considered to be a feature of the present invention.
If it is desired to condition or purify the cellulosic fiber or fabric to be nitrated, it is preferable that such conditioning be effected without ever removing therefrom substantial amounts of the natural moisture, that is, the moisture which remains in the cellulose fiber when it is allowed to air-dry under normal atmospheric conditions. The removal of this water of condition, or water of hygroscopicity, as it is sometimes called, apparently has some deteriorating efiect on cellulosic materials which renders them unsatisfactory for the purposes of the invention. Generally speaking, the water content may vary from about 3% to 12% by weight of the various cellulose materials and, for any particular kind of cellulose, may vary on either side of the average water content by about 1% to 2% by weight within the extreme range ofv ordinary atmospheric conditions.
The composition of the nitrating acid may vary widely. It should preferably be so regulated as to eifect nitration of the fiber or fabric without substantial gelatinization. At the same time, the concentration of nitric acid present should preferably be sumciently high to insure penetration of the fiber or fabric. If nitrating acid of relatively high l-lNOa contentis/ not used initially,
the reaction with the cellulose, which forms water, may dilute the acid to such an extent that the cellulosic fibers are not uniformly nitrated. Also, in the initial treatment of the cellulosic material, if sulfuric acid is used in the nitrating acid, it is desirable that it be present in relatively small amounts, since the formation of cellulose sulfate esters which would. occur to a considerable extent if large proportions of sulfuric acid were present has the effect of weakening the fibers undesirably. On the other hand, a relatively small amount of sulfuric acid may increase the penetrating power of the nitric acid without weakening the fiber substantially. After the cellulosic material has been nitrated to some extent, larger proportions of sulfuric acid appear to aid the nitration without unduly weakening the material. instead of sulfuric acid, the nitrating acid may contain other reagents adapted to increase the penetrating pbwer of the nitric acid, as for example, acetic acid or phosphoric acid.
For the practical application of the nitrating process, it has been found desirable to carry out the nitration in two stages, that is, by two acid treatments. Considerable variation is permissible in the acid composition used for the first treatment. As illustrations of nitrating acids which may be used in this stage may be mentioned anhydrous nitric acid, nitric acid containing water, or a nitric acid-sulfuric acid solution which may contain water. If a nitric acid-water solution is employed, the amount of water present should preferably be less than about 4% by weight. In general, it is preferable to employ a mixed nitric-sulfuric acid solution having an HNQa content of at least about 76% by weight, the remainder being sulfuric acid and/or water (preferably not exceeding 12%).
The composition of the acid solution employed for the second treatment may also. vary within relatively wide limits. It is preferable, however, that the water content of this second acid should vary from about 4% to nightly fuming. The acid content of this second solution should preferably be more than about and less than about 60% EH03, the remainder being H2SO4. Especially desirable results are obtained when the first acid solution contains about 82% to 83% EH03, 7% to 8% H20 and about 10% H2804, and the second acid solution contains about to HNOa and 45% to 50% H2804. Small amounts of mo; may also be present in the acid solutions employed.
The volume of each acid bath should preferably be such that the heat of reaction is'quickly dissipated and that the strength of the acid is maintained nearly uniform in spite of the water formed from the reaction with the cellulose.
Generally speaking, an acid volume corresponding to 60-100 times the weight of the material treated gives satisfactory results.
During the nitration, the temperaturesof the acid baths should preferably be not lower than about 12 C. or higher than about 30 C. The reaction slows up to an undesirable extent when temperatures much lower than 20 C. are utilized and a slowing up of the reaction is particularly disadvantageous for the reason that time is allowed for side reactions. When the temperature utilized exceeds about 30 C., reactions may occur which weaken the fiber or fabric.
While the time of nitration may vary within relatively wide limits depending largely upon the temperatures and concentrations of the acids employed, practical application of the process has demonstrated that the length of time of the im-' mersion in both the first and second acids should be properly controlled. Too short a time of immersion of the material in the first acid ,results in a partial nitration or chemical change which gives undesirable results, while too long an acid treatment may cause gelatinization of the cellulose. A method of procedure which may be used in actual practice involves immersing the material in the first acid until the maximum nitrogen content is obtained without substantial loss of tensile strength.
Close control of the second nitrating step is also import-ant since in this stepthe fibers are subjected to a most intensive nitrating or chemical action. It has been found that the second treatmentis desirable if material having commercial possibilities is to be produced. It is not intended to indicate that cloth which has not been subjected to the second acid treatment has no use.
The cellulosic fiber may have its nitrogen content raised to about 13% in the first treatment,
but such material does not withstand filtration media containing sulfuric or phosphoric acids as well as the after-treated materials.
The method of nitration may be varied widely. It may conveniently'be a so-called pot process in which the nitrating acids are contained in open vessels. The cloth is then immersed in the first acid by suspending it from rods and weighting it at the bottom. After the desired nitration is effected, it is removed from the first acid and transferred to the second acid. In the transfer some of the first acid is carried along. After immersion in the second acid, it may be withdrawn and washed with a stream of water. The finished cloth is preferably preserved in a damp or wet state.
Insofar as is known, nitrated fabrics produced in accordance with the preferred process of this invention are more resistant to acids than a y of the types of filter-cloths previously known. They are particularly advantageous for use in filter press filtrations because in such operations it is desirable that the filter cloth used should possess not only good mechanical strength and resistance to acids but also pliability to the extent that the cloth will return to its original shape when the filter cake has been removed. In a given filter press filtration involving an acidic solution, the improved filter cloths prepared according to the'present invention will last at least seventy times longer than the same cloth unnitrated.
As many apparent and widely different embodiments of this invention may be made without departing from the spiritthereof, it is to be understood that I do not limit myself to the foregoing examples or description except-as indicated in the following claims.
I claim:
1. In a process of producing nitrated cellulosic materials highly resistant to acids, the steps which comprise treating cellulose materials with a nitrating acid sufficiently high in nitric acid and deficient in water and auxiliary penetrating acid, and at a temperature and for a time such that partial nitration is effected without substantially changing the appearance of the material treated and without substantially altering its tensile strength, and continuing the nitration with a more strongly nitrating acid which contains less nitric acid, about 0'4% water and materially more auxiliary penetrating acid than the first acid, until the nitrogen content of the material treated is in excess of 13%.
2. In a process of producing nitrated cellulosic materials highly resistant to acids, the step which comprises nitrating a cellulose material to a nitrogen content in excess of 13% with a nitrating acid containing about 40% to about 60% HNOs,
(l-4% water, the remainder being an auxiliary water, the remainder being sulfuric acid; and,
then treating theresultant product with a nitrating acid containing less than about 4% Water, about 40% to 60% HNOs, the remainder being sulfuric acid.
4. In a process of producing acid resistant materials, the steps which comprise subjecting natural cotton fabrics to the action of a nitricsulfuric acid solution containing more than about 76% by weight HNOa, less than about 12% water, the remainder being sulfuric acid, thereafter treating the resultant product with a nitric-sulfuric acid solution containing less than 4% of water and about 40% to about 60% HNO3.
5. In a process of producing acid resistant materials, the steps which comprise subjecting natural cotton fabrics to the action of an acid solution containing about 82% to 83% HNOS, 7% to 8% H20, and about 10% H2804 and thereafter treating the resultant product with an acid solution containing about 50% to 55% HNO3 and 45% to 50% H2804.
6. The process of producing acid resistant materials which comprises subjecting an undeteriorated cotton fabric to the action of an acid solution containing at least 76% HNOS, not more than 12% water, the remainder being H2504, until the maximum nitrogen content of the product is obtained without substantial loss of tensile strength and thereafter treating the resultant product with a nitric-sulfuric acid solution containing less than about 4% water, and more than about 40% HNOz but less than about 60% HNOs, until the nitrogen content of said product is about 13.4% by weight, while maintaining a ternperature of 20 C. to 30 C. in both acid solutions.
7. The process of producing an acid resistant filter cloth of high tensile strength which comprises immersing unbleached loosely woven cotton cloth containing about 3% to 9% of moisture and which has never been boiled in aqueous solutions, subjected to relatively high temperatures, or in any manner had substantial amounts of the natural moisture removed. therefrom, in an 80 fold volume of a mixed acid solution containing about 83% nitric acid, 11% sulfuric acid and 6% water at a temperature of about C. to C. until the maximum nitrogen content of the product without substantial loss of tensile strength has been obtained, and then removing the resultant cloth from the acid bath. and immediately thereafter submerging it in a substantially anhydrous acid mixture containin about nitric acid and 50% sulfuric acid 1 nitrogen content of the product is about 13.4% by Weight.
8. A nitrated natural cellulosic fabric characterized by the properties that it contains in excess of 13% nitrogen, has practically the same 7 general appearance as the original unnitrated fabric, possesses at least of the tensile strength of the original unnitrated fabric for the same linear width and. retains at least 50% of its tensile strength after being immersed in 0% sulfuric acid for thirty minutes at C.
9. A nitrated natural cellulosic fabric containing about 13.4% nitrogen, characterized by the properties that it possesses at least 85% of the tensile strength of the original unnitrated fabric for the same linear Width and retains at least 50% of its tensile strength after being immersed in %0% sulfuric acid for thirty minutes at 90 C.
10. A nitrated natural cotton fabric containing about 13.4% nitrogen, characterized by the properties that it possesses at least 85% of the tensile strength of the original unnitrated fabric for the same linear width and retains at least 50% of its tensile strength after being immersed in 40% sulfuric acid for thirty minutes at 90 C.
GEORGE E. BRADSHAW.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2416524A (en) * 1943-10-16 1947-02-25 Du Pont Composite filtering medium and method of filtering
US2461632A (en) * 1947-01-24 1949-02-15 Datlow Joseph Method of nitrating cellulose lacebacking fabrics
US2472591A (en) * 1946-03-29 1949-06-07 Eastman Kodak Co Method of preparing an oxidized nitrated cellulose
US2601404A (en) * 1950-04-12 1952-06-24 Thomas S Lasky Oil filter
US4609465A (en) * 1984-05-21 1986-09-02 Pall Corporation Filter cartridge with a connector seal
US7195053B2 (en) 2002-02-06 2007-03-27 Andersen Corporation Reduced visibility insect screen

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2416524A (en) * 1943-10-16 1947-02-25 Du Pont Composite filtering medium and method of filtering
US2472591A (en) * 1946-03-29 1949-06-07 Eastman Kodak Co Method of preparing an oxidized nitrated cellulose
US2461632A (en) * 1947-01-24 1949-02-15 Datlow Joseph Method of nitrating cellulose lacebacking fabrics
US2601404A (en) * 1950-04-12 1952-06-24 Thomas S Lasky Oil filter
US4609465A (en) * 1984-05-21 1986-09-02 Pall Corporation Filter cartridge with a connector seal
US7195053B2 (en) 2002-02-06 2007-03-27 Andersen Corporation Reduced visibility insect screen
US20090104829A1 (en) * 2002-02-06 2009-04-23 Alex Bredemus Reduced Visibility Insect Screen
US8042598B2 (en) 2002-02-06 2011-10-25 Andersen Corporation Reduced visibility insect screen

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