CA2211356C - Ozone-friendly correction fluid with improved overwrite characteristic - Google Patents
Ozone-friendly correction fluid with improved overwrite characteristic Download PDFInfo
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- CA2211356C CA2211356C CA002211356A CA2211356A CA2211356C CA 2211356 C CA2211356 C CA 2211356C CA 002211356 A CA002211356 A CA 002211356A CA 2211356 A CA2211356 A CA 2211356A CA 2211356 C CA2211356 C CA 2211356C
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- Prior art keywords
- phase
- correction fluid
- opacifying
- ozone
- polymeric
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D10/00—Correcting fluids, e.g. fluid media for correction of typographical errors by coating
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Oxygen, Ozone, And Oxides In General (AREA)
- Lubricants (AREA)
Abstract
Generally, the invention relates to an ozone-friendly correction fluid that has improved writeover characteristics. The ozone-friendly correction fluids thus have a key benefit (good writeover characteristic) associated with halogenated hydrocarbon solvent-based correction fluids, but also have the environmental benefits associated with ozone-friendly solvent-based correction fluids. Specifically, the present invention relates to an ozone-friendly correction fluid comprising a non-halogenated hydrocarbon solvent, a polymeric phase and an opacifying phase, wherein the radio of opacifying phase to polymeric phase is from about 2.2 to about 3.8 preferably from about 2.4 to about 3.6 (based on weight).
Description
OZONE-FRIENDLY CORRECTION FLUID WITH IMPROVED
OVERWRITE CHARACTERISTIC
The invention relates to correction fluids.
Correction fluids are used for correcting handwritten, typewritten, photocopied, or laser printed markings on paper. Generally, correction fluids are applied to a paper surface over an erroneous marking in liquid form. The fluid subsequently forms a film which effectively covers erroneous markings on the surface and can receive a correct marking. Making a corrective marking over the film commonly is known as "writeover".
Correction fluids typically include some standard ingredients, including an opacifying pigment (commonly titanium dioxide), a film-forming polymeric material, and a solvent.
The opacifying pigment is dispersed in the fluid and provides the basic white color which can be toned with other pigments to provide a correction fluid closely corresponding to the color of the paper to which the fluid is to be applied. The opacifying pigment functions to obscure the erroneous marking over which the correction fluid is applied.
The film-forming polymeric material, also known as the binder, binds the pigment to the paper and helps to form a flexible but continuous covering that remains once the solvent has dried. r The solvent is used as the carrier for the other ingredients in the fluid. Historically, halogenated hydrocarbons have been the solvents of choice for correction fluid compositions.
Halogenated hydrocarbon solvents present special advantages primarily because they have evaporation rates which provide correction fluids that dry rapidly and completely. Additionally, they do not interact with typewritten markings to cause unacceptable bleeding. Also, they can effectively dissolve those film-forming polymeric materials which provide durable but flexible films without causing excessive cockling or distortion of paper surfaces. Despite their recognized advantages when used as correction fluid solvents, the use of halogenated hydrocarbon solvents has become a matter of increased concern primarily because of their adverse effect on the environment (stratospheric ozone depletion). Accordingly, providing an "ozone-friendly" correction fluid by eliminating the use of halogenated hydrocarbon solvents has become desirable. By ozone-friendly correction fluid, we mean a correction fluid which either does not contain a material that migrates to the stratosphere or, if it contains such a material, the material does not cause a reduction in the ozone concentrations.
Attempts have been made to replace the halogenated solvents with non-halogenated ' alternatives. Aqueous-based systems such as those described in U.S. Patent No. 5,332,599 are not effective for a wide variety of ink formulations.
Alternatively, non-halogenated hydrocarbon solvents, such as those described in U.S. Patent Nos. 5,199,976 and 5,306,755 cover a wide range of ink types, but suffer from poor overwrite characteristics.
It is a object of the present invention to provide a correction fluid based on a non-halogenated solvent system with improved overwrite characteristics.
Generally, the invention relates to an ozone-friendly correction fluid that has improved writeover characteristics. The ozone-friendly correction fluids thus have a key benefit (good writeover characteristic) associated with halogenated hydrocarbon solvent-based correction fluids, but also have the environmental benefits associated with ozone-friendly solvent-based correction fluids.
Specifically, the present invention relates to an ozone-friendly correction fluid comprising a non-halogenated hydrocarbon solvent, a polymeric phase and an opacifying phase. wherein the ratio of opacifying phase to polymeric phase is from about 2.2 to about 3.8 preferably from about 2.4 to about 3.6 (based on weight).
Other features and advantages of the invention will be apparent from the description of the preferred embodiment thereof, and from the claims.
As used herein, the term "overwrite characteristic" relates to a correction fluid films ability to accept new written matter in the form of inks. marker pens and typewriter impacts.
Without being bound to theory, applicants believe that this characteristic is related to film strength and paper adhesion. When correction fluid films exhibit weak strength and poor paper adhesion the overwrite characteristic is extremely poor. This typically results in gouging and flaking of the correction fluid while new pen markings are made on the film. Accordingly, correction fluids which exhibit good "overwrite characteristic" do not exhibit excessive flaking or chipping during normal writing pressures. The E.
importance of a good overwrite characteristic is very important with ink pen and typewriter overwrite due to the relatively high pressures applied. The importance of good overwrite characteristic with marker pens is typically less important.
According to the present invention, it has been discovered that by ratioing the opacifying phase with the polymeric phase of a correction fluid based on a non-halogenated hydrocarbon solvent it is possible to obtain dramatically improved overwrite characteristics.
As used herein, the term "opacifying phase" refers to the total amount of opacifying agent found in the correction fluid. The opacifying agents suitable for use in the present invention include commercially available rutile titanium dioxide, anatase titanium dioxide, zinc sulfide, zinc oxide, calcium carbonate or blends or mixtures of these materials. Preferably the opacifying agent have an average particle size between about 0.2 and about 0.4 microns and an average oil absorption of about 14 lbs. oil/100 lbs. pigment to about 36 lbs. per 100 lbs. The amount of opacifying agent can vary depending on the degree of coverage desired (lower amounts will provide poorer coverage while higher amounts will provide extremely opaque coverage). From about 32 to about 55~ by weight opacifying agent based on the total weight of the composition is generally suitable. Preferably the opacifying agent is selected from the group consisting~of rutile titanium dioxide and anatase titanium dioxide at levels of from about 38 to about 52% by weight based on the total weight of composition.
A,s used. herein, the "polymeric phase"
refers to tlhe film forming binder, (i.e. resin) plasticizer;a, and. dispersants. Hinders suitable for use in 'the present invention include Thez~oplast:ic butyl methacrylate (BMA) copolymer (such as Neocryl B 705 or Neocryl*H700 polymer manufactured by Zeneca Resins, Wilmington, MA or Rohagum*P 6'75 supplied by Rohm Tech Inc., Malden, MA); vinyl toluene-butadiene copolymer (such as those manufactured by Goodyear Chemicals);
isobutyl me~thacrylate polymer (IBMP) (Acryloid*
867, manufactured by Rohm & Haas, Philadelphia, PA); n-buty:L methacrylate polymer (such as Elvacite 2044 manufactured by DuPont Chemical, Wilmington, DE); n-butyl methacrylate/isobutyl methacrylate copolymer (such as Elvacite 2046 manufactured by DuPont Chemical) and mixtures thereof. Suitable "plasticizers" include ditridecyl phthalate. Suitable dispersants include dio<:tyl sodium sulfosuccinate and polymeric fatty ester (Hypermer LPl manufactured by ICI Amer:LCas); and mixtures thereof.
As used herein, suitable "non-halogenated hydrocarbon solvents" include any cyclohexa.ne or alkylated cyclohexane and aliphatic hydrocarbons containing 10 or fewer carbon atoms.
P=eferably the material is methylcyclohexane.
Optionally, correction fluids of the present invention may also include other typical correction fluid ingredients such as tinting colorants, c:.g. lamp black, raw umber, yellow oxide, etc. These tinting colorants are counted as opacifying agents in the "opacifying phase"
calculation.. Also, a small amount of mustard oil * Trade-mark (0.1 - 0.2$) is often added as a deterrent.
According to the present invention, an Opacifying Phase to Polymeric Phase ratio in the range of from 2.2 to 3.8 provides excellent overwrite characteristics when compared with conventional non-halogenated hydrocarbon solvent correction fluid systems. Preferably, the opacifying phase to polymeric phase ratio is from 2.4 to 3.6.
Examples Examples 1-5 below illustrate fluids with Opacifying Phase to Polymeric Phase ratios according to the present invention provide good overwrite properties at high wet fluid lay down, e.g., five mils film thickness. Example 6 below shows a ratio outside the claim range. In use, the Example 6 correction fluid shows inferior overwrite properties at high wet fluid lay down.
Example 1 Ing redients Wt.~
1. Methylcyclohexane 41.41 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 10.78 3. Ditridecyl Phthalate 3.99 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas,, Inc.) 2.22 5. Titanium Dioxide, Tipure R-931 41.39 6. Lamp Black 0.07 7. Mustard Oil 0.12 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacify3.ag 2.44 Phase to Polymeric Phase Ratio:
_ 7 _ l~cample 2 Ing redients Wt.~
1. Methylcyclohe:Kane 42.30 2. Thermoplastic IBMA Copolymer, Neocryl B 70!5 Polymer 9.65 3. Ditridec:yl Phthalate 3.57 4. Polymeric Fati~y Ester, Hyperme:r LP1 (ICI Americas, Inc.) 1.98 5. Titanium Dioxide, Tipure*R-931 42.29 6. Lamp Black 0.07 7. Mustard Oil 0.12 8. Fragrance 759:?92/0602185 (Haarma.nn & Reimer) 0.02 100.00 Opacifying 2.78 Phase t=o Polymeric Phase Ratio:
Example 3 Ing redients Wt.~
1. Methylcyclohexane 40.17 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 9.16 3. Ditridecyl Phthalate 3.39 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.88 5. Titanium; Dioxide, Tipure R-931 45.19 6. Lamp Black 0.08 7. Mustard Oil 0.11 8. Fragrance 759:'92/0602185 (Haarma.nn & Reimer) 0.02 100.00 Pigment 3.13 to Hinder Ratio:
* Trade-mark WO 96/23843 PCTlUS96/01245 _ g _ Example 4 In gredients Wt.%
1. Methylcyclohexane 39.69 , 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 8.52 3. Ditridecyl Phthalate 3.15 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.75 5. Titanium Dioxide, Tipure R-931 46.68 6. Lamp Black 0.08 7. Mustard Oil 0.11 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacifying 3.48 Phase to Polymeric Phase Ratio:
Example 5 Inc tredients Wt . ~
1. Methylcyclohexane 46.21 2. Vinyl Toluene-Butadiene Copolymer (Goodyear Chemicals) 9.68 3. Ditridecyl Phthalate 2.64 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.65 5. Titanium Dioxide, Tipure R-931 39.60 6. Lamp Black 0.07 7. Mustard Oil 0.13 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacifyiag 2.83 Phase E
to Polymeric Phase Ratio:
_ g _ Example 6 IncTredients Snit.
1. Methylcyclohexane 48.91 2. Vinyl Toluene-Butadiene Copolymer (Goodyear Chemicals) 8.53 3. Dioctyl Sodium Sulfosuccinate 1.56 4. Titanium Dioxide, Tipure R-931 40.79 5. Lamp Black 0.07 6. Mustard Oil 0.14 100.00 Opacifying Phase to Polymeric Phase Ratio: 4.04 The correction fluids containing the above ingredients were prepared by first dissolving the binder in the solvent system.
Next, the dispersant, plasticizer and opacifying agent were added and the mixture was dispersed for 3 hours in a bead mill after lamp black and mustard oil were added to obtain final fluid composition.
Other embodiments are within the claims.
For example, in addition to the most preferred ingredients the composition may also include various additives known to those skilled in the art. These additives are incorporated to improve specific properties. These include flattening agents to control film-glow, flow additives and thickeners to control brushing, leveling and ' settling and pigment extenders to reduce cost.
OVERWRITE CHARACTERISTIC
The invention relates to correction fluids.
Correction fluids are used for correcting handwritten, typewritten, photocopied, or laser printed markings on paper. Generally, correction fluids are applied to a paper surface over an erroneous marking in liquid form. The fluid subsequently forms a film which effectively covers erroneous markings on the surface and can receive a correct marking. Making a corrective marking over the film commonly is known as "writeover".
Correction fluids typically include some standard ingredients, including an opacifying pigment (commonly titanium dioxide), a film-forming polymeric material, and a solvent.
The opacifying pigment is dispersed in the fluid and provides the basic white color which can be toned with other pigments to provide a correction fluid closely corresponding to the color of the paper to which the fluid is to be applied. The opacifying pigment functions to obscure the erroneous marking over which the correction fluid is applied.
The film-forming polymeric material, also known as the binder, binds the pigment to the paper and helps to form a flexible but continuous covering that remains once the solvent has dried. r The solvent is used as the carrier for the other ingredients in the fluid. Historically, halogenated hydrocarbons have been the solvents of choice for correction fluid compositions.
Halogenated hydrocarbon solvents present special advantages primarily because they have evaporation rates which provide correction fluids that dry rapidly and completely. Additionally, they do not interact with typewritten markings to cause unacceptable bleeding. Also, they can effectively dissolve those film-forming polymeric materials which provide durable but flexible films without causing excessive cockling or distortion of paper surfaces. Despite their recognized advantages when used as correction fluid solvents, the use of halogenated hydrocarbon solvents has become a matter of increased concern primarily because of their adverse effect on the environment (stratospheric ozone depletion). Accordingly, providing an "ozone-friendly" correction fluid by eliminating the use of halogenated hydrocarbon solvents has become desirable. By ozone-friendly correction fluid, we mean a correction fluid which either does not contain a material that migrates to the stratosphere or, if it contains such a material, the material does not cause a reduction in the ozone concentrations.
Attempts have been made to replace the halogenated solvents with non-halogenated ' alternatives. Aqueous-based systems such as those described in U.S. Patent No. 5,332,599 are not effective for a wide variety of ink formulations.
Alternatively, non-halogenated hydrocarbon solvents, such as those described in U.S. Patent Nos. 5,199,976 and 5,306,755 cover a wide range of ink types, but suffer from poor overwrite characteristics.
It is a object of the present invention to provide a correction fluid based on a non-halogenated solvent system with improved overwrite characteristics.
Generally, the invention relates to an ozone-friendly correction fluid that has improved writeover characteristics. The ozone-friendly correction fluids thus have a key benefit (good writeover characteristic) associated with halogenated hydrocarbon solvent-based correction fluids, but also have the environmental benefits associated with ozone-friendly solvent-based correction fluids.
Specifically, the present invention relates to an ozone-friendly correction fluid comprising a non-halogenated hydrocarbon solvent, a polymeric phase and an opacifying phase. wherein the ratio of opacifying phase to polymeric phase is from about 2.2 to about 3.8 preferably from about 2.4 to about 3.6 (based on weight).
Other features and advantages of the invention will be apparent from the description of the preferred embodiment thereof, and from the claims.
As used herein, the term "overwrite characteristic" relates to a correction fluid films ability to accept new written matter in the form of inks. marker pens and typewriter impacts.
Without being bound to theory, applicants believe that this characteristic is related to film strength and paper adhesion. When correction fluid films exhibit weak strength and poor paper adhesion the overwrite characteristic is extremely poor. This typically results in gouging and flaking of the correction fluid while new pen markings are made on the film. Accordingly, correction fluids which exhibit good "overwrite characteristic" do not exhibit excessive flaking or chipping during normal writing pressures. The E.
importance of a good overwrite characteristic is very important with ink pen and typewriter overwrite due to the relatively high pressures applied. The importance of good overwrite characteristic with marker pens is typically less important.
According to the present invention, it has been discovered that by ratioing the opacifying phase with the polymeric phase of a correction fluid based on a non-halogenated hydrocarbon solvent it is possible to obtain dramatically improved overwrite characteristics.
As used herein, the term "opacifying phase" refers to the total amount of opacifying agent found in the correction fluid. The opacifying agents suitable for use in the present invention include commercially available rutile titanium dioxide, anatase titanium dioxide, zinc sulfide, zinc oxide, calcium carbonate or blends or mixtures of these materials. Preferably the opacifying agent have an average particle size between about 0.2 and about 0.4 microns and an average oil absorption of about 14 lbs. oil/100 lbs. pigment to about 36 lbs. per 100 lbs. The amount of opacifying agent can vary depending on the degree of coverage desired (lower amounts will provide poorer coverage while higher amounts will provide extremely opaque coverage). From about 32 to about 55~ by weight opacifying agent based on the total weight of the composition is generally suitable. Preferably the opacifying agent is selected from the group consisting~of rutile titanium dioxide and anatase titanium dioxide at levels of from about 38 to about 52% by weight based on the total weight of composition.
A,s used. herein, the "polymeric phase"
refers to tlhe film forming binder, (i.e. resin) plasticizer;a, and. dispersants. Hinders suitable for use in 'the present invention include Thez~oplast:ic butyl methacrylate (BMA) copolymer (such as Neocryl B 705 or Neocryl*H700 polymer manufactured by Zeneca Resins, Wilmington, MA or Rohagum*P 6'75 supplied by Rohm Tech Inc., Malden, MA); vinyl toluene-butadiene copolymer (such as those manufactured by Goodyear Chemicals);
isobutyl me~thacrylate polymer (IBMP) (Acryloid*
867, manufactured by Rohm & Haas, Philadelphia, PA); n-buty:L methacrylate polymer (such as Elvacite 2044 manufactured by DuPont Chemical, Wilmington, DE); n-butyl methacrylate/isobutyl methacrylate copolymer (such as Elvacite 2046 manufactured by DuPont Chemical) and mixtures thereof. Suitable "plasticizers" include ditridecyl phthalate. Suitable dispersants include dio<:tyl sodium sulfosuccinate and polymeric fatty ester (Hypermer LPl manufactured by ICI Amer:LCas); and mixtures thereof.
As used herein, suitable "non-halogenated hydrocarbon solvents" include any cyclohexa.ne or alkylated cyclohexane and aliphatic hydrocarbons containing 10 or fewer carbon atoms.
P=eferably the material is methylcyclohexane.
Optionally, correction fluids of the present invention may also include other typical correction fluid ingredients such as tinting colorants, c:.g. lamp black, raw umber, yellow oxide, etc. These tinting colorants are counted as opacifying agents in the "opacifying phase"
calculation.. Also, a small amount of mustard oil * Trade-mark (0.1 - 0.2$) is often added as a deterrent.
According to the present invention, an Opacifying Phase to Polymeric Phase ratio in the range of from 2.2 to 3.8 provides excellent overwrite characteristics when compared with conventional non-halogenated hydrocarbon solvent correction fluid systems. Preferably, the opacifying phase to polymeric phase ratio is from 2.4 to 3.6.
Examples Examples 1-5 below illustrate fluids with Opacifying Phase to Polymeric Phase ratios according to the present invention provide good overwrite properties at high wet fluid lay down, e.g., five mils film thickness. Example 6 below shows a ratio outside the claim range. In use, the Example 6 correction fluid shows inferior overwrite properties at high wet fluid lay down.
Example 1 Ing redients Wt.~
1. Methylcyclohexane 41.41 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 10.78 3. Ditridecyl Phthalate 3.99 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas,, Inc.) 2.22 5. Titanium Dioxide, Tipure R-931 41.39 6. Lamp Black 0.07 7. Mustard Oil 0.12 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacify3.ag 2.44 Phase to Polymeric Phase Ratio:
_ 7 _ l~cample 2 Ing redients Wt.~
1. Methylcyclohe:Kane 42.30 2. Thermoplastic IBMA Copolymer, Neocryl B 70!5 Polymer 9.65 3. Ditridec:yl Phthalate 3.57 4. Polymeric Fati~y Ester, Hyperme:r LP1 (ICI Americas, Inc.) 1.98 5. Titanium Dioxide, Tipure*R-931 42.29 6. Lamp Black 0.07 7. Mustard Oil 0.12 8. Fragrance 759:?92/0602185 (Haarma.nn & Reimer) 0.02 100.00 Opacifying 2.78 Phase t=o Polymeric Phase Ratio:
Example 3 Ing redients Wt.~
1. Methylcyclohexane 40.17 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 9.16 3. Ditridecyl Phthalate 3.39 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.88 5. Titanium; Dioxide, Tipure R-931 45.19 6. Lamp Black 0.08 7. Mustard Oil 0.11 8. Fragrance 759:'92/0602185 (Haarma.nn & Reimer) 0.02 100.00 Pigment 3.13 to Hinder Ratio:
* Trade-mark WO 96/23843 PCTlUS96/01245 _ g _ Example 4 In gredients Wt.%
1. Methylcyclohexane 39.69 , 2. Thermoplastic IBMA Copolymer, Neocryl B 705 Polymer 8.52 3. Ditridecyl Phthalate 3.15 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.75 5. Titanium Dioxide, Tipure R-931 46.68 6. Lamp Black 0.08 7. Mustard Oil 0.11 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacifying 3.48 Phase to Polymeric Phase Ratio:
Example 5 Inc tredients Wt . ~
1. Methylcyclohexane 46.21 2. Vinyl Toluene-Butadiene Copolymer (Goodyear Chemicals) 9.68 3. Ditridecyl Phthalate 2.64 4. Polymeric Fatty Ester, Hypermer LP1 (ICI Americas, Inc.) 1.65 5. Titanium Dioxide, Tipure R-931 39.60 6. Lamp Black 0.07 7. Mustard Oil 0.13 8. Fragrance 759292/0602185 (Haarmann & Reimer) 0.02 100.00 Opacifyiag 2.83 Phase E
to Polymeric Phase Ratio:
_ g _ Example 6 IncTredients Snit.
1. Methylcyclohexane 48.91 2. Vinyl Toluene-Butadiene Copolymer (Goodyear Chemicals) 8.53 3. Dioctyl Sodium Sulfosuccinate 1.56 4. Titanium Dioxide, Tipure R-931 40.79 5. Lamp Black 0.07 6. Mustard Oil 0.14 100.00 Opacifying Phase to Polymeric Phase Ratio: 4.04 The correction fluids containing the above ingredients were prepared by first dissolving the binder in the solvent system.
Next, the dispersant, plasticizer and opacifying agent were added and the mixture was dispersed for 3 hours in a bead mill after lamp black and mustard oil were added to obtain final fluid composition.
Other embodiments are within the claims.
For example, in addition to the most preferred ingredients the composition may also include various additives known to those skilled in the art. These additives are incorporated to improve specific properties. These include flattening agents to control film-glow, flow additives and thickeners to control brushing, leveling and ' settling and pigment extenders to reduce cost.
Claims (6)
1. A correction fluid comprising: a non-halogenated hydrocarbon solvent; a polymer phase and an opacifying phase, wherein the ratio of opacifying phase to polymeric phase is from 2.2 to 3.6 based on weight.
2. A correction fluid of claim 1 wherein said solvent is selected from the group consisting of: cyclohexane; an alkylated cyclohexane; an aliphatic hydrocarbon containing 10 or fewer carbon atoms; and mixtures thereof.
3. A correction fluid of claim 2 wherein said opacifying phase consists of a material selected from the group consisting of rutile titanium dioxide, anatase titanium dioxide, zinc sulfide, zinc oxide, calcium carbonate blends and mixtures of these materials.
4. A correction fluid of claim 3 wherein said polymeric phase is comprised of a resin material selected from the group consisting of thermoplastic butyl methacrylate, vinyl toluene-butadiene copolymer, isobutyl methacrylate polymer, n-butyl methacrylate/isobutyl methacrylate copolymer and mixtures thereof.
5. A correction fluid of claim 4 wherein said polymeric phase further comprising a ditridecyl phthalate plasticizer.
6. A correction fluid of claim 5 wherein said polymer phase further comprises a dispersant selected from the group consisting of dioctyl sodium sulfosuccinate, polymeric fatty ester and mixtures thereof.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38105295A | 1995-01-31 | 1995-01-31 | |
| US381,052 | 1995-01-31 | ||
| PCT/US1996/001245 WO1996023843A1 (en) | 1995-01-31 | 1996-01-26 | Ozone-friendly correction fluid with improved overwrite characteristic |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2211356A1 CA2211356A1 (en) | 1996-08-08 |
| CA2211356C true CA2211356C (en) | 2002-08-06 |
Family
ID=23503463
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002211356A Expired - Fee Related CA2211356C (en) | 1995-01-31 | 1996-01-26 | Ozone-friendly correction fluid with improved overwrite characteristic |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP0807147A1 (en) |
| JP (1) | JPH10513216A (en) |
| CN (1) | CN1087329C (en) |
| AR (1) | AR000844A1 (en) |
| AU (1) | AU715675B2 (en) |
| BR (1) | BR9606869A (en) |
| CA (1) | CA2211356C (en) |
| CO (1) | CO4560379A1 (en) |
| PL (1) | PL321751A1 (en) |
| RU (1) | RU2154080C2 (en) |
| SG (1) | SG42918A1 (en) |
| TR (1) | TR199600082A2 (en) |
| TW (1) | TW408164B (en) |
| WO (1) | WO1996023843A1 (en) |
| ZA (1) | ZA96482B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6083618A (en) * | 1997-06-25 | 2000-07-04 | The Gillette Company | Correction fluids comprising composite polymeric particles |
| CN101238185A (en) | 2005-08-04 | 2008-08-06 | 桑福德有限合伙人公司 | Correction fluids |
| CN101400747B (en) * | 2006-04-01 | 2011-11-16 | 派通株式会社 | Retouching fluid and coating tool using the same |
| CN102295852A (en) * | 2010-06-25 | 2011-12-28 | 张红雨 | Universal correction fluid |
| US9109126B2 (en) | 2013-07-22 | 2015-08-18 | Sanford, L.P. | Ink compositions comprising colorant particles containing polymeric particles |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58141254A (en) * | 1982-02-16 | 1983-08-22 | Zebura Kk | Correcting ink |
| US5199976A (en) * | 1991-06-13 | 1993-04-06 | The Gillette Company | Ozone-friendly correction fluid |
| US5306755A (en) * | 1992-04-09 | 1994-04-26 | The Gillette Company | Correction fluid containing a butyl methacrylate copolymer ditridecyl phthalate, a non-halogenated solvent and an opacifying agent |
-
1996
- 1996-01-22 ZA ZA96482A patent/ZA96482B/en unknown
- 1996-01-26 JP JP8523676A patent/JPH10513216A/en not_active Ceased
- 1996-01-26 CN CN96191710A patent/CN1087329C/en not_active Expired - Fee Related
- 1996-01-26 CA CA002211356A patent/CA2211356C/en not_active Expired - Fee Related
- 1996-01-26 AU AU49093/96A patent/AU715675B2/en not_active Ceased
- 1996-01-26 WO PCT/US1996/001245 patent/WO1996023843A1/en not_active Application Discontinuation
- 1996-01-26 EP EP96905287A patent/EP0807147A1/en not_active Withdrawn
- 1996-01-26 BR BR9606869A patent/BR9606869A/en not_active Application Discontinuation
- 1996-01-26 PL PL96321751A patent/PL321751A1/en unknown
- 1996-01-26 RU RU97114942/04A patent/RU2154080C2/en active
- 1996-01-30 CO CO96003782A patent/CO4560379A1/en unknown
- 1996-01-31 TR TR96/00082A patent/TR199600082A2/en unknown
- 1996-01-31 SG SG1996000678A patent/SG42918A1/en unknown
- 1996-01-31 AR ARP960101217A patent/AR000844A1/en unknown
- 1996-03-12 TW TW085102944A patent/TW408164B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| BR9606869A (en) | 1997-12-23 |
| AR000844A1 (en) | 1997-08-06 |
| EP0807147A1 (en) | 1997-11-19 |
| WO1996023843A1 (en) | 1996-08-08 |
| RU2154080C2 (en) | 2000-08-10 |
| AU715675B2 (en) | 2000-02-10 |
| SG42918A1 (en) | 1997-10-17 |
| CA2211356A1 (en) | 1996-08-08 |
| AU4909396A (en) | 1996-08-21 |
| CN1172494A (en) | 1998-02-04 |
| CN1087329C (en) | 2002-07-10 |
| PL321751A1 (en) | 1997-12-22 |
| MX9705830A (en) | 1997-11-29 |
| CO4560379A1 (en) | 1998-02-10 |
| TW408164B (en) | 2000-10-11 |
| ZA96482B (en) | 1996-08-13 |
| JPH10513216A (en) | 1998-12-15 |
| TR199600082A2 (en) | 1996-08-21 |
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