US3808038A - Formed article of cellulose acetate treated with organic titanium chelate compounds - Google Patents

Formed article of cellulose acetate treated with organic titanium chelate compounds Download PDF

Info

Publication number
US3808038A
US3808038A US11848771A US3808038A US 3808038 A US3808038 A US 3808038A US 11848771 A US11848771 A US 11848771A US 3808038 A US3808038 A US 3808038A
Authority
US
United States
Prior art keywords
cellulose acetate
titanium chelate
organic titanium
carbon atoms
chelate compound
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
Inventor
N Minagawa
W Ueno
H Kawaguchi
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.)
Fujifilm Holdings Corp
Original Assignee
Fuji Photo Film Co Ltd
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 Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Application granted granted Critical
Publication of US3808038A publication Critical patent/US3808038A/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
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/85Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/003Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31971Of carbohydrate

Definitions

  • Cited articles are generated by incorporation into or on the UNITED STATES PATENTS article of an organic titanium chelate compound.
  • This invention relates to an antistatic method for formed articles of cellulose acetate. More particularly, it is concerned with a method of preventing static troubles by adding an organic titanium chelate compound to cellulose acetate and then forming the article or by treating the surface of a formed article of cellulose acetate with a solution of an organic titanium chelate compound in an organic solvent.
  • R and R are alkyl groups of or 4 carbon atoms
  • R is a hydrogen atom, an alkyl group of from 1 to 4'carbon atoms, or an aryl group of from 6 to 10 carbon atoms
  • R R and R are hydrogen atoms or alkyl groups of from 1 to 4 carbon atoms and R is an alkoxyl group of from 1 to 4 carbon atoms or an aryl group of from 6 to 10 carbon atoms
  • R and R are alkyl groups of 3 or 4 carbon atoms
  • R is an alkyl group of from 1 to 4 carbon atoms or an aryl group of from 6 to 10 carbon atoms
  • R is a hydrogen atom or an alkyl group of from 1 to 4 carbon atoms
  • R is an alkyl group of from 1 to 4 carbon atoms, an aryl group of from 6 to 10 carbon atoms, or an alkoxyl group of from 1 to 4 carbon
  • the titanium chelate compounds can be obtained by reacting a titanium alkoxide with at least one of the keto-alcohols, aldehyde-alcohols and dicarbonyl compounds having an active hydrogen.
  • the organic titanium chelate compound used in the invention reacts with the hydroxyl groups remaining in the cellulose acetate forming a strong chemical bond. Therefore, it is not removed by friction or water washing and the antistatic effect does not deteriorate with the passage of time.
  • a titanium alkoxide obtained by reacting titanium tetrachloride with a monohydric alcohol is too reactive to be stable. For example, it is immediately converted into titanium dioxide by a microamount of water in a solvent or by the moisture in the air.
  • the organic titanium chelate compound of the invention is so stable that it does not require a particularly dehydrated solvent and is not changed when left in the air.
  • the organic titanium chelate compound of the invention can be obtained by reacting a titanium alkoxide with one or more organic compounds capable of forming the chelate compound, such as aldehyde-alcohols, keto-alcohols and dicarbonyl compounds having active hydrogens.
  • Suitable titanium alkoxides which can be used are tetraisopropyl titanate and tetrabutyl titanate.
  • a suitable aldehyde-alcohol which can be used is B-hydroxybutyraldehyde and suitable ketoalcohols which can be used are diacetone alcohol and 'y-ketobutanol.
  • the titanium alkoxide is reacted with the aldehyde alcohol and/or keto alcohol thus obtaining the above-described organic titanium chelate compound having the General Formula A.
  • dicarbonyl compounds having active hydrogens which can be used are acetylacetone, acetoacetic acid ester, benzoylacetone and benzoylacetic acid ester.
  • the titanium alkoxide is reacted with the dicarbonyl compound having an active hydrogen thus obtaining the above-described organic titanium chelate compound having the General Formula B.
  • these compounds may be added to the cellulose acetate which is formed into pellets followed by molding or may be applied in the form of a solution, dispersion or emulsion to the surface of a formed article of cellulose acetate.
  • the invention utilizes the fact that the static generating property of cellulose acetate can be varied by adding an organ ic titanium chelate compound to or coating an organic titanium chelate compound onto a surface. Static charge can be suppressed while the static generating characteristics are varied appropriately depending on the quantity of the organic titanium chelate compound added or coated. Therefore, it is advantageous in that the quantity of the organic titanium chelate compound used can be varied freely so as to reduce the magnitude of the static generation depending on the kind of objects which will be subjected to friction or which may come into contact with other objects.
  • the disadvantages encountered with the prior art method wherein the surface electric resistance of the formed article to be treated is lowered by a surfactant can be overcome, that is, that the treated layer on the surface is readily stripped off by friction or removed by water washing or the antistatic agent exudes on the surface.
  • the static charge can be prevented permanently without deteriorating the quality of the formed article.
  • the foregoing cellulose acetate solution was at room temperature flowed, spread and dried.
  • the resulting film was stripped from a support and held at 1 10C for 2 hours to remove the residual solvent.
  • the charge on frictional contact with a rubber roller and the surface electric resistivity of the thus obtained cellulose acetate film are shown in Table l, at a relative humidity of 65 percent.
  • the amount of the organic titanium chelate compound added to the cellulose acetate (acetic acid bonded 60.7 percent) was adjusted to 0.7 g/l00 g cellulose acetate thereby completely preventing the friction charge with rubber.
  • EXAMPLE 3 1.75 g of the organic titanium chelate compound having the above-described structural formula, synthesized from tetraisopropyl titanate and benzoylacetophenone, was dissolved in a mixed solvent consisting of 100 g of methylene chloride, 200 g of methyl ethyl ketone and 50 g of isopropanol, coated onto a film of cellulose acetate (acetic acid bonded 55.0 percent) and dried at C for 5 minutes. The composition of the resulting coating solution corresponded to a concentration of the organic titanium chelate compound of 0.5 percent by weight. Where it is desired to vary the concentration of the coating solution, the amount of the organic titanium chelate compound can be varied while holding the composition and amount of the solvent constant. Coating and drying conditions are also constant.
  • a concentration of about 0.5 percent is effective to prevent a charge on frictional contact with a rubber roller.
  • EXAMPLE 4 The organic titanium chelate compound, synthesized from tetrabutyl titanate and B-hydroxybutyraldehyde, was added to a film of cellulose acetate (acetic acid bonded 55.0 percent) in a manner similar to that of Example 1. The charge on frictional contact with a rubber roller and the surface electric resistivity were measured at a relative humidity of 65 percent, with the results obtained being shown in Table 4.
  • a cellulose acetate article having anti-static characteristics comprising cellulose acetate having coated thereon or incorporated therein an anti-statically effective amount of an organic titanium chelate compound selected from the group consisting of titanium chelate compounds having the general formula A:
  • R, and R are alkyl groups of 4 carbon atoms
  • R is selected from the group consisting of a hydrogen atom, an alkyl group of from 1 to 4 carbon atoms, and an aryl group of from 6 to 10 carbon atoms
  • R R and R are selected from the group consisting of hydrogen atoms and alkyl groups of from 1 to 4 carbon atoms
  • R is selected from the group consisting of an alkoxyl group of from 1 to 4 carbon atoms and an aryl group of from 6 to 10 carbon atoms
  • B having the general formula B:
  • R and R are alkyl groups of 4 carbon atoms
  • R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms and an aryl group of from 6 to 10 carbon atoms
  • R is selectedfromthe group consisting of a hydrogen atom and an alkyl group of from 1 to 4 carbon atoms
  • R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms, an aryl group of from 6 to 10 carbon atoms
  • R and R are alkyl groups of 4 carbon atoms
  • R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms and an aryl group of from 6 to 10 carbon atoms
  • R is selected from the group consisting of a hydrogen atom and an alkyl group of from 1 to 4 carbon atoms
  • R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms, an aryl group of from 6 to 10 carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)

Abstract

Anti-static characteristics for formed cellulose acetate articles are generated by incorporation into or on the article of an organic titanium chelate compound.

Description

Haslam 117/144 X United States Patent [1 1 1111 3,808,038 Ueno et al. Apr. 30, 1974 [5 FORMED ARTICLE OF CELLULOSE 2,525,049 10/1950 Signaigo 117/144 x ACETATE TREATED WITH ORGANIC 2,658,000 1 1/1953 Sullivan et al. 1 17/144 X TITANIUM CHELATE Cob/[POUNDS 2,788,295 4/1957 Cooke et al. 1 17/144 X [75] Inventors: Wataru Ueno, Kanagawa; Hideo FOREIGN PATENTS OR APPLICATIONS Kawaguchi; Nobuhiko Minagawa, 557,905 5/1958 Canada 106/ 169 7 both of Sh1zu0ka, all of Japan OTHER PUBLICATIONS [73] ASSgnee: Fuji Photo Feld et al., The Organic Chemistry of Titanium, 1965,
Nakanuma, Japan pp. 58-68, 174-183. [22] Filed: Feb. 24, 1971 Hist, R. P., et al., Polyfunctional lsocyanatest Titanium Organics as Cross-Linking Agents for Cellulose [21] Appl' Derivatives, Ind. & Engr. Chemistry, vol. 48, N0. 8,
Aug., 1956, P. 1,325. [30] Foreign Application Priority Data Feb. 24, 1970 Japan 45-15706 Primary Examiner-William D. Martin Assistant Examiner-M. R. Lusignan [52] US. Cl 117/144, 106/ 169, 106/189, Attorney, Agent, or Firm-Sughrue, Rothwell, Mion,
106/196 Zinn & Macpeak [51] Int. Cl. C08j H38 [58] Field of Search 117/144, 159; 106/169,
106/196, 189 [57] ABSTRACT Anti-static characteristics for formed cellulose acetate 5 References Cited articles are generated by incorporation into or on the UNITED STATES PATENTS article of an organic titanium chelate compound.
2,768,909 10/1956 1 Claim, No Drawings FORMED ARTICLE OF CELL ULOSE ACETATE TREATED WITH ORGANIC TITANIUM CI-IELATE COMPOUNDS BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to an antistatic method for formed articles of cellulose acetate. More particularly, it is concerned with a method of preventing static troubles by adding an organic titanium chelate compound to cellulose acetate and then forming the article or by treating the surface of a formed article of cellulose acetate with a solution of an organic titanium chelate compound in an organic solvent.
2. Description of the Prior Art Some antistatic methods for plastics hitherto have been proposed, for example, by reducing the generation of static charges on the surface of the plastics due to friction or contact with another object, or lowering the electric resistance of the surface of plastics to increase the dissipation of the static charges. The latter method has been carried out completely.
We, the inventors, have conducted research on antistatic methods for formed articles of cellulose acetate for a long time and have invented the following antistatic method, which relates to the reducing of the generation of staticcharges on the surface.
SUMMARY OF THE INVENTION in whichR and R are alkyl groups of or 4 carbon atoms, R is a hydrogen atom, an alkyl group of from 1 to 4'carbon atoms, or an aryl group of from 6 to 10 carbon atoms, R R and R are hydrogen atoms or alkyl groups of from 1 to 4 carbon atoms and R is an alkoxyl group of from 1 to 4 carbon atoms or an aryl group of from 6 to 10 carbon atoms, and General Forr'riulaB in which R and R are alkyl groups of 3 or 4 carbon atoms, R is an alkyl group of from 1 to 4 carbon atoms or an aryl group of from 6 to 10 carbon atoms, R, is a hydrogen atom or an alkyl group of from 1 to 4 carbon atoms, R is an alkyl group of from 1 to 4 carbon atoms, an aryl group of from 6 to 10 carbon atoms, or an alkoxyl group of from 1 to 4 carbon atoms.
The titanium chelate compounds can be obtained by reacting a titanium alkoxide with at least one of the keto-alcohols, aldehyde-alcohols and dicarbonyl compounds having an active hydrogen.
DETAILED DESCRIPTION OF THE INVENTION The organic titanium chelate compound used in the invention reacts with the hydroxyl groups remaining in the cellulose acetate forming a strong chemical bond. Therefore, it is not removed by friction or water washing and the antistatic effect does not deteriorate with the passage of time.
A titanium alkoxide obtained by reacting titanium tetrachloride with a monohydric alcohol is too reactive to be stable. For example, it is immediately converted into titanium dioxide by a microamount of water in a solvent or by the moisture in the air. On the contrary, the organic titanium chelate compound of the invention is so stable that it does not require a particularly dehydrated solvent and is not changed when left in the air.
I The organic titanium chelate compound of the invention can be obtained by reacting a titanium alkoxide with one or more organic compounds capable of forming the chelate compound, such as aldehyde-alcohols, keto-alcohols and dicarbonyl compounds having active hydrogens. Suitable titanium alkoxides which can be used, for example, are tetraisopropyl titanate and tetrabutyl titanate. A suitable aldehyde-alcohol which can be used is B-hydroxybutyraldehyde and suitable ketoalcohols which can be used are diacetone alcohol and 'y-ketobutanol. The titanium alkoxide is reacted with the aldehyde alcohol and/or keto alcohol thus obtaining the above-described organic titanium chelate compound having the General Formula A.
Examples of the dicarbonyl compounds having active hydrogens which can be used are acetylacetone, acetoacetic acid ester, benzoylacetone and benzoylacetic acid ester. The titanium alkoxide is reacted with the dicarbonyl compound having an active hydrogen thus obtaining the above-described organic titanium chelate compound having the General Formula B.
In the antistatic method of the invention, these compounds may be added to the cellulose acetate which is formed into pellets followed by molding or may be applied in the form of a solution, dispersion or emulsion to the surface of a formed article of cellulose acetate.
The invention utilizes the fact that the static generating property of cellulose acetate can be varied by adding an organ ic titanium chelate compound to or coating an organic titanium chelate compound onto a surface. Static charge can be suppressed while the static generating characteristics are varied appropriately depending on the quantity of the organic titanium chelate compound added or coated. Therefore, it is advantageous in that the quantity of the organic titanium chelate compound used can be varied freely so as to reduce the magnitude of the static generation depending on the kind of objects which will be subjected to friction or which may come into contact with other objects.
ln accordance with the method of this invention, the disadvantages encountered with the prior art method wherein the surface electric resistance of the formed article to be treated is lowered by a surfactant can be overcome, that is, that the treated layer on the surface is readily stripped off by friction or removed by water washing or the antistatic agent exudes on the surface. When a formed article is treated according to the invention, the static charge can be prevented permanently without deteriorating the quality of the formed article.
The following examples are given to illustrate the invention in greater detail without limiting the scope of the invention.
EXAMPLE 1 H: C O O i l-CH:
The organic titanium chelate compound having the above-described structural formula, synthesized from tetrabutyl titanate and diacetone alcohol, was added to cellulose acetate (acetic acid bonded 60.7 percent) using the following procedure. 25 g of cellulose acetate (acetic acid bonded 60.7 percent) was dissolved in a mixed solvent consisting of 18 g of n-butanol and 207 g of methylene chloride. After the dissolving was completed, 0.25 g of the above-described organic titanium chelate compound was dissolved in g of methylene chloride, added and mixed with adequate agitation. The composition of the resulting solution corresponded to 1.0 g of organic titanium chelate compound/100 g of cellulose acetate. Where it is desired to vary the content of the organic titanium chelate compound, the concentration of the organic titanium chelate compound in methylene chloride solution can be varied while holding constant the ratio of the cellulose acetate and each solvent.
The foregoing cellulose acetate solution was at room temperature flowed, spread and dried. The resulting film was stripped from a support and held at 1 10C for 2 hours to remove the residual solvent. The charge on frictional contact with a rubber roller and the surface electric resistivity of the thus obtained cellulose acetate film are shown in Table l, at a relative humidity of 65 percent. The amount of the organic titanium chelate compound added to the cellulose acetate (acetic acid bonded 60.7 percent) was adjusted to 0.7 g/l00 g cellulose acetate thereby completely preventing the friction charge with rubber.
TABLE 1 Amount of Organic EXAMPLE 2 ll C() 02115 TABLE 2 Amount of Organic Titanium Chelate Surface Compound Added Charge on Frictional Electric (g/IUO g cellulose Contact with Rubber Resistiv|ty acetate) Roller (V) ((1) 0.0 +29 1.3 10" 0.25 +13 7.5 X 10'" 0.50 2 7.4 X 10' L0 6 7 2 X10121 6 9.4 x 10" As is evident from these results, the added amount of 0.5 g/ g cellulose acetate is effective so as to reduce the charge on frictional contact with rubber roller.
EXAMPLE 3 1.75 g of the organic titanium chelate compound having the above-described structural formula, synthesized from tetraisopropyl titanate and benzoylacetophenone, was dissolved in a mixed solvent consisting of 100 g of methylene chloride, 200 g of methyl ethyl ketone and 50 g of isopropanol, coated onto a film of cellulose acetate (acetic acid bonded 55.0 percent) and dried at C for 5 minutes. The composition of the resulting coating solution corresponded to a concentration of the organic titanium chelate compound of 0.5 percent by weight. Where it is desired to vary the concentration of the coating solution, the amount of the organic titanium chelate compound can be varied while holding the composition and amount of the solvent constant. Coating and drying conditions are also constant.
The charge on frictional contact with a rubber roller and the surface electric resistivity of the thus treated film were measured at a relative humidity of 65 percent to obtain the results shown in Table 3.
As is evident from these results, a concentration of about 0.5 percent is effective to prevent a charge on frictional contact with a rubber roller.
EXAMPLE 4 The organic titanium chelate compound, synthesized from tetrabutyl titanate and B-hydroxybutyraldehyde, was added to a film of cellulose acetate (acetic acid bonded 55.0 percent) in a manner similar to that of Example 1. The charge on frictional contact with a rubber roller and the surface electric resistivity were measured at a relative humidity of 65 percent, with the results obtained being shown in Table 4.
TABLE 4 Amount of Organic The organic titanium chelate compound synthesized from tetraisopropyl titanate and acetylacetone was coated onto a film of cellulose acetate (acetic acid bonded 60.7 percent) using the same procedure as described in Example 3 and the charge on frictional contact with a rubber roller and the surface electric resistivity were measuredat a relative humidity of 65 percent with the results obtained being shown in Table 5.
TABLE 5 Surface Concentration of Charge on Frictional Electric Coating Solution Contact with Rubber Resistivity (wt Roller (V) (O) 0.0 l' 28 4.5 X 0.5 4 8.9 X 10' 1.0 e 6 9.0 X 10' 2.0 5 7.5 X 10" What is claimed is:
l. A cellulose acetate article having anti-static characteristics comprising cellulose acetate having coated thereon or incorporated therein an anti-statically effective amount of an organic titanium chelate compound selected from the group consisting of titanium chelate compounds having the general formula A:
General Formula A wherein R, and R are alkyl groups of 4 carbon atoms, R is selected from the group consisting of a hydrogen atom, an alkyl group of from 1 to 4 carbon atoms, and an aryl group of from 6 to 10 carbon atoms, R R and R are selected from the group consisting of hydrogen atoms and alkyl groups of from 1 to 4 carbon atoms, and R is selected from the group consisting of an alkoxyl group of from 1 to 4 carbon atoms and an aryl group of from 6 to 10 carbon atoms, and having the general formula B:
General Formula B wherein R and R are alkyl groups of 4 carbon atoms, R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms and an aryl group of from 6 to 10 carbon atoms, R, is selectedfromthe group consisting of a hydrogen atom and an alkyl group of from 1 to 4 carbon atoms and R is selected from the group consisting of an alkyl group of from 1 to 4 carbon atoms, an aryl group of from 6 to 10 carbon atoms, and
an alkoxyl group of from 1 to 4 carbon atoms.
US11848771 1970-02-24 1971-02-24 Formed article of cellulose acetate treated with organic titanium chelate compounds Expired - Lifetime US3808038A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1570670A JPS4823541B1 (en) 1970-02-24 1970-02-24

Publications (1)

Publication Number Publication Date
US3808038A true US3808038A (en) 1974-04-30

Family

ID=11896198

Family Applications (1)

Application Number Title Priority Date Filing Date
US11848771 Expired - Lifetime US3808038A (en) 1970-02-24 1971-02-24 Formed article of cellulose acetate treated with organic titanium chelate compounds

Country Status (4)

Country Link
US (1) US3808038A (en)
JP (1) JPS4823541B1 (en)
FR (1) FR2079013A5 (en)
GB (1) GB1318334A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3899613A (en) * 1972-11-04 1975-08-12 Fuji Photo Film Co Ltd Static charge preventing method for acetylcellulose moldings
US4146669A (en) * 1976-04-06 1979-03-27 Tsentralny Nauchno-Issledovatelsky Institut Bumagi (Tsniib) Crosslinking agent, method of producing same and paper made with the use thereof

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5129067U (en) * 1974-08-27 1976-03-02
DE3134709A1 (en) * 1981-09-02 1983-03-10 Byk Gulden Lomberg Chemische Fabrik Gmbh, 7750 Konstanz ANTINEOPLASTIC TITANIUM COMPOUND AND MEDICINAL PRODUCTS CONTAINING THEM
DE3565254D1 (en) * 1984-06-30 1988-11-03 Huels Troisdorf TITAN (IV) -ACETYL ACETONATES

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2525049A (en) * 1946-08-22 1950-10-10 Du Pont Cellulose titanate film production
US2658000A (en) * 1951-05-31 1953-11-03 Nat Lead Co Solution for treatment of fibrous cellulosic materials
US2768909A (en) * 1953-07-28 1956-10-30 Du Pont Method of coating surface with transparent film and product resulting therefrom
US2788295A (en) * 1953-11-12 1957-04-09 American Cyanamid Co Titania monohydrate soil retarding treatment of textiles
CA557905A (en) * 1958-05-27 Canadian Titanium Pigments Limited Coating solution containing a cellulose compound and an alkyl titanate

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA557905A (en) * 1958-05-27 Canadian Titanium Pigments Limited Coating solution containing a cellulose compound and an alkyl titanate
US2525049A (en) * 1946-08-22 1950-10-10 Du Pont Cellulose titanate film production
US2658000A (en) * 1951-05-31 1953-11-03 Nat Lead Co Solution for treatment of fibrous cellulosic materials
US2768909A (en) * 1953-07-28 1956-10-30 Du Pont Method of coating surface with transparent film and product resulting therefrom
US2788295A (en) * 1953-11-12 1957-04-09 American Cyanamid Co Titania monohydrate soil retarding treatment of textiles

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Feld et al., The Organic Chemistry of Titanium, 1965, pp. 58 68, 174 183. *
Hist, R. P., et al., Polyfunctional Isocyanatest Titanium Organics as Cross Linking Agents for Cellulose Derivatives, Ind. & Engr. Chemistry, Vol. 48, No. 8, Aug., 1956, P. 1,325. *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3899613A (en) * 1972-11-04 1975-08-12 Fuji Photo Film Co Ltd Static charge preventing method for acetylcellulose moldings
US4146669A (en) * 1976-04-06 1979-03-27 Tsentralny Nauchno-Issledovatelsky Institut Bumagi (Tsniib) Crosslinking agent, method of producing same and paper made with the use thereof

Also Published As

Publication number Publication date
GB1318334A (en) 1973-05-31
JPS4823541B1 (en) 1973-07-14
FR2079013A5 (en) 1971-11-05

Similar Documents

Publication Publication Date Title
US5443944A (en) Photographic material
US4015050A (en) Plastics film with an aluminium phosphate coating
US3100704A (en) Photographic materials containing carbodhmides
EP0440957B1 (en) New polythiophene dispersions, their preparation and their use
US3519462A (en) Method of impregnating polymethyl methacrylate
US2874046A (en) Process for the retreatment of foils consisting of highly polymeric substances for the application of hydrophilic colloids
US3839078A (en) Method of coating substrates
US3337357A (en) New ultra-violet light stabilized compositions, processes for preparing same and uses thereof
US2720468A (en) Process for gelling
US3808038A (en) Formed article of cellulose acetate treated with organic titanium chelate compounds
US3741782A (en) Stabilized zirconium salts
US3005728A (en) Cellulosic laminates
DE2935616A1 (en) METHOD FOR CURING AN ORGANOALKOXYSILANE COMPOUND
US4438176A (en) Thermoplastic coated films with anti-static properties
US3573216A (en) Heterocyanoacrylate u.v. absorbers
US2343186A (en) Fireproofing plasticizers
US5209931A (en) Stabilized pvc products and their production
DE2544841A1 (en) METHOD FOR ANTISTATIC TREATMENT OF A LIGHT SENSITIVE PHOTOGRAPHIC SILVER HALOGENIDE MATERIAL
US3210312A (en) Anti-electrostatic imidazoline salts for resin compositions
US3362958A (en) 4-[pyrazolyl-(1)]-naphthalimides
US3870519A (en) S-triazine derivatives as ultraviolet protecting agents
US2415631A (en) Photographic paper
US3625692A (en) Photographic material having slippageimproving additive in surface coating
US2514131A (en) Process of producing sheetings of a water-soluble film-forming material
US2584337A (en) Antistatic treating composition for photographic film supports