US2543086A - Method of preparing dustless photographic fixing powders - Google Patents

Method of preparing dustless photographic fixing powders Download PDF

Info

Publication number
US2543086A
US2543086A US787617A US78761747A US2543086A US 2543086 A US2543086 A US 2543086A US 787617 A US787617 A US 787617A US 78761747 A US78761747 A US 78761747A US 2543086 A US2543086 A US 2543086A
Authority
US
United States
Prior art keywords
dust
particles
parts
anhydrous sodium
powder
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
Application number
US787617A
Inventor
Edwin S Wiitala
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US787617A priority Critical patent/US2543086A/en
Priority to FR980404D priority patent/FR980404A/en
Application granted granted Critical
Publication of US2543086A publication Critical patent/US2543086A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/38Fixing; Developing-fixing; Hardening-fixing
    • G03C5/386Hardening-fixing

Definitions

  • This invention relates to photographic fixing powders and more particularly to dustless substantially anhydrous fixing powders and the method for their preparation.
  • One method of preparing photographic fixing powders comprises thoroughly mixing several anhydrous chemicals in a conical "blender! Among the chemicals usually found in the acid fixer the most prominent dust contributor is the anhydrous sodium thiosuliate. Other chemicals that produce dust particles include sodium acetate, sodium bisulfite, and boric acid. This dust conditon presents a definite hazard to the photographic trade due to potential contamination of sensitive emulsions and darkroom areas, and
  • the principal object of this invention is to obv ate the above-mentioned dust defects of acid fixing powders and to provide a method of preparing these acid fixing powders which eliminates such dust from occurring in the fixing powder.
  • Another object is to provide an acid fixing powder containing substantially no dust-like particles.
  • a further object is to prepare a substantially anhydrous fixing powder which has improved solubility characteristics.
  • these and other objects are attained by adding to the fixing powder mixture one or more components which contain water of hydration.
  • the hydrated component is introduced into the mixture in a dry state and consequently can be dispersed uniformly throughout the fixing powder mixture.
  • the mixture is then heated to a temperature suf- .ficient to release water of hydration which is thus uniformly distributed throughout the fixing powder. .
  • only the particularly active dust-forming components need be thus treated, and other substantially dust-free components can be subsequently added to the composition.
  • the resu t ng fixing powder is about 99 percent dust free, whereas the same mixture without the moisture-releasing step is only 88 percent dust free. Since the moisture is uniformly distributed. there is less possibility of localized 'sulfurization reactions taking place as could be the case were the moisture added by other means. Drying is also more easily accomplished since there are no localized high concentrations of moisture present which may cause lumping and a non-uniformly dried product.
  • My process has the advantages in thatit is possible to control accurately the amount of moisture addition; a very uniform distribution of available moisture is hadj th'e'resulting product does not form a hard cake when put in solution; an increased rate of solution is experienced; the uniform moisture distribution afiords a more uniform and complete drying, and a considerably more complete elimination of dust than results by other methods; on prolonged standing or aging in containers the granular product does not cake or thiosulfate.
  • Example 1 A substantially anhydrous dustfree fixing powder containing:
  • Sodium thiosulfate pentahydrate 20 is prepared in accordance with my invention as follows: A mixture containing the anhydrous sodium thiosulfate, the sodium thiosulfate pentahydrate, anhydrous sodium bisulfite, and sodium acetate is tumbled in a closed mixer which is adapted to be heated in minutes to 120 F. to release the water of hydration of the sodium This heating andtumbling eliminates dust particles and the remaining components of the formula are then thoroughly mixed into the composition. . The resulting granular product is found to be 99.9 percent free of dust. A mixed sample of this formula without the dust-eliminating or heating step is only 88 percent free from dust. The treated composition was easily soluble in water, whereas the untreated composition tended to cake and dissolvedslowly in water.
  • Example 2 The formula shown in Example 1 is added together to a closed mixer and then mixed and heated in minutes to 110 F. The mixture is then cooled and was found to be 99.9 percent free of dust. The resulting fixing powder was easily soluble in water.
  • Example 3 The formula shown in Example 1 is mixed as follows in order to prepare a dustless fixing powder.
  • the anhydrous sodium thiosulfate is preheated to 135 F. in the mixer and then the remaining components at a temperature of about 70 F. are added to the mixer and mixed for 15 minutes with the thiosulfate.
  • the resulting temperature is about 110 F. which is suflicient to liberate some residual moisture in the chemicals as well as some water of hydration in the alum.
  • the mix is not sulfurized and on cooling was found to be 99.0 percent free of dust.
  • Example 4 To preheated anhydrous sodium thiosulfate, which has been heated in the mixer to 135 F., are added the other components in the fixing formula of Example 1 (excluding the sodium thiosulfate pentahydrate) except that percent of the sodium acetate is in the form of sodium acetate trihydrate. Mixing was conducted at 110 F. for 20 minutes, and on cooling to room temperature the resulting fixing powder was found to be 99.9 percent dust free.
  • Example 5 pounds of the acid fixing powder mixture containing:
  • the dustiness of the various fixing powders was determined in an air elutriation unit. This unit involves a slow fiow of air at 18 ft. per minute through a 10.-inch"square duct into which is fed the material;to be dust tested from a vibrating feed trough at the rate of 0.5 gm. per minute. The dustiest particles falling from the top of theduct will travel farther down the horizontal duct than the dustless particles before settling to its bottom. The rate of fall is dependent upon particle density and shape.
  • the bottom of the duct is covered with aluminum trough-like plates to facilitate removal of the obtained fractions. The plates are graduated from the point of feed as follows: 1, 5, 14, 30, and 52 inches. This graduation results in plates of 1, 4, 9, 16, and 22 inches in length, respectively. It was found that particles falling on the last two plates are particularly objectionable. The particles have a flat cylindrical shape and have diameters of lessthan 1 to 80 microns.
  • dust particles I mean particles of one or more components of the fixing powder.
  • the fixing powder resulting from my invention may be termed substantially anhydrous and by that term I mean that the product contains only moisture resulting from the release of water of hydration from those components containing water of hydration. This amount of water may be as highas 10-15% of the composition, although generally only 5% is present. This water content compares favorably with the moisture in fixing powders. made by former methods which moisture may be as high as 40%.
  • the method of forming a substantially anhydrous, dust-free photographic fixing powder which comprises thoroughly mixing together in a closed mixer While heating to F. in 20 minutes, 5 parts boric acid, 10 parts anhydrous sodium bisulfite, 147 parts anhydrous sodium thiosulfate, 22.5 parts anhydrous sodium acetate, 22.5 parts potassium alum, 20 parts sodium thiosulfate pentahydrate, said ingredients being in a powder form and comprising relatively large particles and relatively minute dust-like particles, said heating causing the release of water of hydration from said pentahydrate, and resulting in binding said minute dust-like particles to the larger particles thereby substantially reducing the. dustiness of the fixing powder.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Detergent Compositions (AREA)

Description

Patented Feb. 27, 1951 AMETHOD 0F PREPARING DUSTLESS QHOTOGBAPHIC FIXING PQVYDERS Edwin S. Wiitala, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application November 22, 1947, Serial No. 787,617
2 Claims. (Cl. 95-88) This invention relates to photographic fixing powders and more particularly to dustless substantially anhydrous fixing powders and the method for their preparation.
At the present time there is a considerable demand in the photographic trade for anhydrous fixing powders. These fixing powders are made up of a mixture of several chemicals, both inorganic and organic, many of which comprise such fine particles that they are inherently dusty and cause d ifiiculty in handling during the preparation of the fixing powder as well as when the photographer employs them. In the latter case, unless special care is employed. the dust may fall upon other photographic elements in the vicinity and cause damage.
One method of preparing photographic fixing powders comprises thoroughly mixing several anhydrous chemicals in a conical "blender! Among the chemicals usually found in the acid fixer the most prominent dust contributor is the anhydrous sodium thiosuliate. Other chemicals that produce dust particles include sodium acetate, sodium bisulfite, and boric acid. This dust conditon presents a definite hazard to the photographic trade due to potential contamination of sensitive emulsions and darkroom areas, and
consequently the photographer must exercise particu ar care when opening the package and employing the powder so as not to stir up dust.
The principal object of this invention is to obv ate the above-mentioned dust defects of acid fixing powders and to provide a method of preparing these acid fixing powders which eliminates such dust from occurring in the fixing powder.
Another object is to provide an acid fixing powder containing substantially no dust-like particles.
A further object is to prepare a substantially anhydrous fixing powder which has improved solubility characteristics.
In accordance with the invention, these and other objects are attained by adding to the fixing powder mixture one or more components which contain water of hydration. The hydrated component is introduced into the mixture in a dry state and consequently can be dispersed uniformly throughout the fixing powder mixture. The mixture is then heated to a temperature suf- .ficient to release water of hydration which is thus uniformly distributed throughout the fixing powder. .If desired, only the particularly active dust-forming components need be thus treated, and other substantially dust-free components can be subsequently added to the composition.
This internal release of moisture apparently bonds the fine dust-like particles of the chemical to other particles of the mixture which are relatively larger. While the exact theory of the bonding action has not been established, possibly the bonding includes two different operations, which result in the granulated product. In one, the released water of hydration actually dissolves the small dust particles whose solution is deposited on other large crystals, and in this manner crystal growth is obtained and the dust particles eliminated. By the other operation, the hydrate crystals may form a nucleus of moisture on which the fine particles adhere. The product at any rate is agglomerated, whatever the mechanism, and may then be dried further to prevent caking and a possible sulfurization reaction on prolonged standing. The degree of drying is dependent upon the amount of moisture added as hydrate and that already present in the product.
The resu t ng fixing powder is about 99 percent dust free, whereas the same mixture without the moisture-releasing step is only 88 percent dust free. Since the moisture is uniformly distributed. there is less possibility of localized 'sulfurization reactions taking place as could be the case were the moisture added by other means. Drying is also more easily accomplished since there are no localized high concentrations of moisture present which may cause lumping and a non-uniformly dried product. My process has the advantages in thatit is possible to control accurately the amount of moisture addition; a very uniform distribution of available moisture is hadj th'e'resulting product does not form a hard cake when put in solution; an increased rate of solution is experienced; the uniform moisture distribution afiords a more uniform and complete drying, and a considerably more complete elimination of dust than results by other methods; on prolonged standing or aging in containers the granular product does not cake or thiosulfate.
lump, as may be the case in wet binders; and the product has the appearance of a single powder chemical.
The following examples illustrate my novel process for preparing anhydrous acid fixing powders.
Example 1.--A substantially anhydrous dustfree fixing powder containing:
Parts Boric acid Anhydrous sodium bisulfite Anhydrous sodium thiosulfate 147 Anhydrous sodium acetate 22.5 Potassium alum 22.5 Sodium thiosulfate pentahydrate 20 is prepared in accordance with my invention as follows: A mixture containing the anhydrous sodium thiosulfate, the sodium thiosulfate pentahydrate, anhydrous sodium bisulfite, and sodium acetate is tumbled in a closed mixer which is adapted to be heated in minutes to 120 F. to release the water of hydration of the sodium This heating andtumbling eliminates dust particles and the remaining components of the formula are then thoroughly mixed into the composition. .The resulting granular product is found to be 99.9 percent free of dust. A mixed sample of this formula without the dust-eliminating or heating step is only 88 percent free from dust. The treated composition was easily soluble in water, whereas the untreated composition tended to cake and dissolvedslowly in water.
Example 2.-The formula shown in Example 1 is added together to a closed mixer and then mixed and heated in minutes to 110 F. The mixture is then cooled and was found to be 99.9 percent free of dust. The resulting fixing powder was easily soluble in water.
Example 3.The formula shown in Example 1 is mixed as follows in order to prepare a dustless fixing powder. The anhydrous sodium thiosulfate is preheated to 135 F. in the mixer and then the remaining components at a temperature of about 70 F. are added to the mixer and mixed for 15 minutes with the thiosulfate. The resulting temperature is about 110 F. which is suflicient to liberate some residual moisture in the chemicals as well as some water of hydration in the alum. The mix is not sulfurized and on cooling was found to be 99.0 percent free of dust.
Example 4.-To preheated anhydrous sodium thiosulfate, which has been heated in the mixer to 135 F., are added the other components in the fixing formula of Example 1 (excluding the sodium thiosulfate pentahydrate) except that percent of the sodium acetate is in the form of sodium acetate trihydrate. Mixing was conducted at 110 F. for 20 minutes, and on cooling to room temperature the resulting fixing powder was found to be 99.9 percent dust free.
Example 5.'25 pounds of the acid fixing powder mixture containing:
Parts Boric acid 5 Anhydrous sodium bisulfite 12.5 Anhydrous sodium thiosulfate 290.0 Anhydrous sodium acetate 22.5 Sodium thiosulfate pentahydrate 9 were tumbled in a closed mixer for one hour at 130 F. The resulting tacky product was then dried for 14 hours in a tray at 125 F. under Parts Boric acid 5 Anhydrous sodium bisulfite 12.5 Anhydrous sodium thiosulfate 282 Anhydrous sodium acetate 30 Sodium thiosulfate pentahydrate 27 were tumbled in a closed mixer for one hour at 130 F. The resulting tacky product was then dried for 14 hours in a tray at 125 F. under vacuum. This mixture was uniformly blended with 20 parts of ammonium alum.
Dust measurement on this material showed it to be 99.9 percent free of dust.
The dustiness of the various fixing powders was determined in an air elutriation unit. This unit involves a slow fiow of air at 18 ft. per minute through a 10.-inch"square duct into which is fed the material;to be dust tested from a vibrating feed trough at the rate of 0.5 gm. per minute. The dustiest particles falling from the top of theduct will travel farther down the horizontal duct than the dustless particles before settling to its bottom. The rate of fall is dependent upon particle density and shape. The bottom of the duct is covered with aluminum trough-like plates to facilitate removal of the obtained fractions. The plates are graduated from the point of feed as follows: 1, 5, 14, 30, and 52 inches. This graduation results in plates of 1, 4, 9, 16, and 22 inches in length, respectively. It was found that particles falling on the last two plates are particularly objectionable. The particles have a flat cylindrical shape and have diameters of lessthan 1 to 80 microns.
It will be understood that in referring to dust particles I. mean particles of one or more components of the fixing powder.
The fixing powder resulting from my invention may be termed substantially anhydrous and by that term I mean that the product contains only moisture resulting from the release of water of hydration from those components containing water of hydration. This amount of water may be as highas 10-15% of the composition, although generally only 5% is present. This water content compares favorably with the moisture in fixing powders. made by former methods which moisture may be as high as 40%.
I claim:
1. The method of forming a substantially anhydrous dust-free photographic fixing powder tion whereby the dust-like particles the com- 1 position are bound to the larger particles of the powder. 7
2. The method of forming a substantially anhydrous, dust-free photographic fixing powder which comprises thoroughly mixing together in a closed mixer While heating to F. in 20 minutes, 5 parts boric acid, 10 parts anhydrous sodium bisulfite, 147 parts anhydrous sodium thiosulfate, 22.5 parts anhydrous sodium acetate, 22.5 parts potassium alum, 20 parts sodium thiosulfate pentahydrate, said ingredients being in a powder form and comprising relatively large particles and relatively minute dust-like particles, said heating causing the release of water of hydration from said pentahydrate, and resulting in binding said minute dust-like particles to the larger particles thereby substantially reducing the. dustiness of the fixing powder.
EDWIN S. WIITALA.
6 REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,753,059 Murray Apr. 1, 1930 2,074,200 Barth et a1 Mar. 16, 1937 2,101,834 Bean Dec. 14, 1937 2,378,248 Russell et a1. June 12, 1945 2,414,969 Moose Jan. 28, 1947 2,477,492 Moose July 26, 1949

Claims (1)

1. THE METHOD OF FORMING A SUBSTANTIALLY ANHYDROUS DUST-FREE PHOTOGRAPHIC FIXING POWDER WHICH COMPRISES THOROUGHLY MIXING 5 PARTS BORIC ACID, 10 PARTS ANHYDROUS SODIUM BISULFITE, 147 PARTS ANHYDROUS SODIUM THIOSULFATE, 22.5 PARTS ANHYDROUS SODIUM ACETATE, 22.5 PARTS POTASSIUM ALUM, 20 PARTS SODIUM THIOSULFATE PENTAHYDRATE, SAID INGREDIENTS BEING IN POWDERED FORM AND COMPRISING RELATIVELY LARGE PARTICLES AND RELATIVELY MINUTE DUST-LIKE PARTICLES AND THEN HEATING THE MIXTURE TO RELEASE THE WATER OF HYDRATION WHEREBY THE DUST-LIKE PARTICLES IN THE COMPOSITION ARE BOUND TO THE LARGER PARTICLES OF THE POWDER.
US787617A 1947-11-22 1947-11-22 Method of preparing dustless photographic fixing powders Expired - Lifetime US2543086A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US787617A US2543086A (en) 1947-11-22 1947-11-22 Method of preparing dustless photographic fixing powders
FR980404D FR980404A (en) 1947-11-22 1948-11-22 Powder photographic fixatives and process for their preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US787617A US2543086A (en) 1947-11-22 1947-11-22 Method of preparing dustless photographic fixing powders

Publications (1)

Publication Number Publication Date
US2543086A true US2543086A (en) 1951-02-27

Family

ID=25142044

Family Applications (1)

Application Number Title Priority Date Filing Date
US787617A Expired - Lifetime US2543086A (en) 1947-11-22 1947-11-22 Method of preparing dustless photographic fixing powders

Country Status (2)

Country Link
US (1) US2543086A (en)
FR (1) FR980404A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2871121A (en) * 1955-12-14 1959-01-27 Kimura Shuji Photographic fixer-hardener compositions
US5055384A (en) * 1989-05-10 1991-10-08 Agfa Gevaert Aktiengesellschaft Granulated photographic fixative and its preparation
US5135840A (en) * 1990-03-23 1992-08-04 Agfa Gevaert Aktiengesellschaft Granulated photochemicals

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1753059A (en) * 1928-07-14 1930-04-01 Norton And Gregory Ltd Production of photographic images
US2074200A (en) * 1935-02-08 1937-03-16 Agfa Ansco Corp Prepared chemicals and method of preparing the same
US2101834A (en) * 1936-01-29 1937-12-14 Eastman Kodak Co Compositions of matter for photographic processing baths
US2378248A (en) * 1942-09-26 1945-06-12 Eastman Kodak Co Photographic art
US2414969A (en) * 1943-03-13 1947-01-28 Monsanto Chemicals Process for producing agglomerated water treating compositions
US2477492A (en) * 1943-12-03 1949-07-26 Monsanto Chemicals Agglomerated water treating composition and method of producing same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1753059A (en) * 1928-07-14 1930-04-01 Norton And Gregory Ltd Production of photographic images
US2074200A (en) * 1935-02-08 1937-03-16 Agfa Ansco Corp Prepared chemicals and method of preparing the same
US2101834A (en) * 1936-01-29 1937-12-14 Eastman Kodak Co Compositions of matter for photographic processing baths
US2378248A (en) * 1942-09-26 1945-06-12 Eastman Kodak Co Photographic art
US2414969A (en) * 1943-03-13 1947-01-28 Monsanto Chemicals Process for producing agglomerated water treating compositions
US2477492A (en) * 1943-12-03 1949-07-26 Monsanto Chemicals Agglomerated water treating composition and method of producing same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2871121A (en) * 1955-12-14 1959-01-27 Kimura Shuji Photographic fixer-hardener compositions
US5055384A (en) * 1989-05-10 1991-10-08 Agfa Gevaert Aktiengesellschaft Granulated photographic fixative and its preparation
US5135840A (en) * 1990-03-23 1992-08-04 Agfa Gevaert Aktiengesellschaft Granulated photochemicals

Also Published As

Publication number Publication date
FR980404A (en) 1951-05-11

Similar Documents

Publication Publication Date Title
US5055384A (en) Granulated photographic fixative and its preparation
JPH02109042A (en) Granular color photographic developer and manufacture thereof
US3565658A (en) Carbon black dispersing agent
ATE35422T1 (en) PROCESSES FOR THE PREPARATION OF PIGMENT COMPOSITIONS.
US3692529A (en) Process of oiling
US2543086A (en) Method of preparing dustless photographic fixing powders
US4029820A (en) Tracers
US3086833A (en) Diazonium salt compositions and method
US2744823A (en) Salt composition
US2421185A (en) Dustless salt and process
US4425170A (en) Desensitizing explosives
US3644215A (en) Process for converting liquid antioxidants to pulverulent form
US3558299A (en) Process for rendering particulate urea substantially noncaking and composition
US3981713A (en) Urea-zinc oxide composition and process
US2788280A (en) Water repellent materials and process of producing the same
US2407805A (en) Explosive composition
US2739167A (en) Stabilized, oil-soluble vitamins and process of preparing the same
US2835602A (en) Cementitious mixes
US2850553A (en) Stabilized benzothiazolesulfenamide composition and method of preparing the same
US2685513A (en) Method of stabilizing hydrates of sodium metaborate and single powder photographic developers containing same
ES282900A1 (en) Procedure for the preparation of a finally divided wax composition containing a herbicide material (Machine-translation by Google Translate, not legally binding)
US2592366A (en) Noncaking photographic acid fixing powders
US2973257A (en) Propellent powder
US3335097A (en) Digestion catalyst
DE69321899T2 (en) PRODUCTION OF FLOWABLE ALKALI OR AMMONIUM THIOSULFATE OR SULFIT AND PRODUCT BY THIS PROCESS