US3427277A - Method of making pressure-sensitive liquid-dispensing device from polyamides and article therefrom - Google Patents
Method of making pressure-sensitive liquid-dispensing device from polyamides and article therefrom Download PDFInfo
- Publication number
- US3427277A US3427277A US504218A US3427277DA US3427277A US 3427277 A US3427277 A US 3427277A US 504218 A US504218 A US 504218A US 3427277D A US3427277D A US 3427277DA US 3427277 A US3427277 A US 3427277A
- Authority
- US
- United States
- Prior art keywords
- liquid
- polyamide
- ink
- polyamides
- solvent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004952 Polyamide Substances 0.000 title description 34
- 229920002647 polyamide Polymers 0.000 title description 33
- 238000004519 manufacturing process Methods 0.000 title description 5
- 239000000976 ink Substances 0.000 description 25
- 239000007788 liquid Substances 0.000 description 25
- 239000002904 solvent Substances 0.000 description 21
- 239000000203 mixture Substances 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 15
- 229920001778 nylon Polymers 0.000 description 11
- 239000004677 Nylon Substances 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 238000001816 cooling Methods 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000499 gel Substances 0.000 description 7
- 150000005846 sugar alcohols Polymers 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- MXAOILAHPVJWBS-UHFFFAOYSA-N 10-(azepan-1-yl)-10-oxodecanamide Chemical compound NC(=O)CCCCCCCCC(=O)N1CCCCCC1 MXAOILAHPVJWBS-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- DJZKNOVUNYPPEE-UHFFFAOYSA-N tetradecane-1,4,11,14-tetracarboxamide Chemical compound NC(=O)CCCC(C(N)=O)CCCCCCC(C(N)=O)CCCC(N)=O DJZKNOVUNYPPEE-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- -1 e.g. Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000001788 irregular Effects 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002781 deodorant agent Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- CKIGNOCMDJFFES-UHFFFAOYSA-N n-naphthalen-2-yl-1-phenylmethanimine Chemical compound C=1C=C2C=CC=CC2=CC=1N=CC1=CC=CC=C1 CKIGNOCMDJFFES-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 235000012544 Viola sororia Nutrition 0.000 description 1
- 241001106476 Violaceae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000019241 carbon black Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- YYGBVRCTHASBKD-UHFFFAOYSA-M methylene green Chemical compound [Cl-].C1=CC(N(C)C)=C([N+]([O-])=O)C2=[S+]C3=CC(N(C)C)=CC=C3N=C21 YYGBVRCTHASBKD-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/88—Polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41K—STAMPS; STAMPING OR NUMBERING APPARATUS OR DEVICES
- B41K1/00—Portable hand-operated devices without means for supporting or locating the articles to be stamped, i.e. hand stamps; Inking devices or other accessories therefor
- B41K1/36—Details
- B41K1/38—Inking devices; Stamping surfaces
- B41K1/54—Inking pads
Definitions
- Micro-porous gel-like irregular, unsymmetrical polyamide and liquid which is a non-solvent at room temperature and solvent at elevated temperature.
- Method of manufacture involves heating mixture to form a homogeneous liquid and cooling to gel.
- a substance to be dispensed from the gel, e.g., ink, is dispersed in the liquid.
- This invention relates to compositions, and methods for other manufacture, that have a self-contained supply of fluid material that will be expressed from the composition upon the application of pressure.
- compositions of this sort may be useful in dispensing numerous liquids such as inks, perfumes, deodorants, medicinal agents, and other like materials. While it should be understood that these devices may contain any such useful liquids, for simplicity, the invention will be described hereinafter with specific regard to ink filled materials that are particularly adapted for use as ink pads, ink rolls, marking stamps, printing platens, self-ink type, etc. It will be understood, however, that this is not done by way of limitation and that the invention is equally applicable to other liquid fillers which are intended to be included within the scope hereof.
- Porous inking devices and structures are known to the prior art. Ordinarily, these devices are filled or impregnated with the inking medium only after they are in substantially finished form. It has also been proposed to produce inking devices having liquid-retaining regions, and with or without liquid ink present therein, with the aid of pore-forming agents. Further, vinyl plastisol and organosol compositions containing an incompatible inking vehicle in the fused state have also been used to produce a fused inking device.
- An object of this invention is to provide a method of making a pressure-sensitive liquid-dispensing device.
- Another object of this invention is to provide a polyamide inking device having a long useful life with controlled exudation of ink to give very sharp images.
- a further object of this invention is to provide a method "ice of making a composition, and the composition per se, with liquid-dispensing properties.
- a further object of this invention is to provide a composition useful in making liquid-dispensing devices.
- the method involves mixing a powdered polyamide with a liquid which is a non-solvent for the polyamide at room temperature, but which is a solvent for the polyamide at elevated temperatures, and with a dye or pigment soluble in or dispersi'ble in the solvent; heating the mixture thus formed, with or without agitation, to a temperature and for a time sufficient to dissolve said polyamide and form a homogeneous liquid; then cooling the homogeneous liquid to room temperature to produce a micro-porous pressure-sensitive ink-containing and -exuding gel-like structure.
- the hot homogeneous liquid can be poured, extruded, injection molded, or otherwise formed into the desired shape and configuration prior to cooling.
- Example I The following materials were used in this example: Ethylene glycol cc 60 Methyl violet base A dye gm 2 61 nylon gm 10 Nylon blendE gm l0 1 61 nylon is a polyamide interpolymer or copolymer of part hexamethylene adipamide, ,4; part hexamethylene sebacamide, and part caprol-actam. This was used in the form of a finely divided powder.
- a finely powdered blend of 60% type 6/6 nylon and 40% type 6 nylon is provided.
- the ethylene glycol was poured into a beaker and the methyl violet dye was stirred into it.
- the 61 nylon was then added to the beaker and stirred until wetted out, then the nylon blend E was added and stirred until wetted out.
- One of the trays was preheated to approximately 'F. prior to pouring. After cooling, the resulting ink pads were used with conventional rubber stamps having molded raised letters and numerals.
- the transfer of ink from the ink pad to the rubber stamp was quite smoothly and easily accomplished with only slight application of pressure and the rubber stamp produced good, clear impressions.
- the stamp pad made in the preheated mold produced a slightly better ink pad.
- the pore size of the ink pads was in the range of from about 1 to about 3 microns.
- Example II The procedure and composition described in Example I were employed in this example with the exception that 72 cc. of ethylene glycol were used instead of 60 cc. and 3 gms. of methyl violet dye used instead of the previous 2 gms.
- the resulting ink pads were tough, had a pore size of about 1 to about 3 microns, and readily transferred ink to a stamp when applied against the surface of the ink pad.
- the stamp produced excellent impressions and imprints on many different grades of paper.
- Example III The following materials were used in this example:
- Ethylene glycol cc 36 Propylene glycol cc 36 Methyl violet base
- a dye gms 8 61 nylon gms 10 Nylon blend E gms 20 The ethylene glycol and propylene glycol were placed in a beaker together with the dye and stirred until the dye was wetted out. The powdered nylons were then added with continued stirring until they were wetted out. The mixture was heated to approximately 350 F. and stirring continued until all lumps disappeared and a resulting freefiowing, homogeneous liquid was produced. This liquid was then poured into preheated roll molds and then cooled to form a gel.
- This procedure produced an ink or inking roller which is useful for printing names and addresses or other indicia on sales slips or the like with a printing apparatus of the type shown in US. Patent 2,620,730.
- a portable printing plate having raised characters is supported by one of two opposed members, the inking roller being carried by the other of said opposed members.
- a sales slip or the like, with or without a plurality of carbons, is interposed between the opposed members and the roller is then moved in a path substantially contiguous with the raised characters are imprinted upon the sales slip with one or more carbons also being produced, if desired.
- the inking roller of Example III exuded ink from its surface only in those areas corresponding to the raised characters of the printing plate thereby giving a clear, legible impression without smearing or blotting.
- homogeneous liquid is intended to cover and include true molecular solutions as well as colloidal dispersions.
- the cooling operation may be carried out in molds which are at room temperature or with moderately preheated molds, e.g., preheated to a temperature of about 120-180 F.
- a preferred class of polyamides that may be mentioned as being particularly suitable for use in this invention are those that are prepared by the amidization of polyfunctional amines, which preferably are at least trifunctional, and may be aliphatic, alicyclic or aromatic, and a mixture of diand trifunctional acids that have been produced from unsaturated fatty acids or their esters by reductive oligomerization, Other 0f the known polyamides of at least moderate molecular weight and mixtures thereof may be useful in this invention, and their initial selection may be based upon the above noted characteristics of low crystallinity and a wide softening or melting point range. The final choice of the particular polyamide used will depend upon the hardness and other properties desired in the final product.
- polystyrene foams are copolymers and interpolymers.
- One such commercially available polyamide is prepared from approximately equal portions of hexamethylene adipamide, hexamethylene sebacamide and caprolactam (sold under the trade designation nylon 61 by DuPont).
- a suitable solvent for use with a particular polyamide in forming the gel may also be of importance.
- the solvent is selected for its ability to solvate the polyamide at elevated temperatures as well as for its ability to form a relatively strong, stable gel.
- solvents that are suitable for use in the practice of this invention, there may be mentioned alcohols, and especially the polyhydric alcohols such as ethylene, propylene and hexylene glycol, glycerine, and especially triethylene glycol.
- swelling agents such as epoxies and dioctylphthalate may .be used effectively in some instances.
- the proportion of solvent to polymer can be varied over wide limits depending upon the physical characteristics desired of the finished device. Generally, the proportions of polyhydric alcohol solvent will vary from 25 to 75% by weight of the entire composition.
- the finished product may be more suitable for use if supplied in a cross-linked state, either throughout the structure or merely a surface cross-linking, and to that end, minor amounts of known polyamide crosslinking agents may be employed.
- dyes which may be used as the coloring or inking material for example, methyl violet, methylene blue, methylene green, etc.
- pigments dispersible in the polyhydric alcohol e.g., carbon black, ultramarine blues and violets, chrome oxide greens, etc.
- the device of the present invention can be used to exude or transfer ingredients other than ink.
- ingredients dispersible or soluble in the polyhydric alcohol solvent, e.g., perfumes, deodorants, medicinal agents, etc.
- a method of forming a pressure-sensitive liquiddispensing device that has a self-contained reservoir of a first liquid which comprises:
- polyhydric alcohol is ethylene glycol, propylene glycol, triethylene glycol, glycerine, or mixtures thereof.
- polyamide is an interpolymer consisting essentially of the polymerization product of hexamethylene adipamide, hexamethylene sebacamide, and caprolactam.
- a form stable, pressure-sensitive, liquid-dispensing, gel-like structure comprised of a polyamide and a liquid that is a solvent for the polyamide at elevated temperatures and a nonsolvent at room temperatures wherein the polyamide is an interpolymer consisting essentially molar portions of hexamethylene adipamide, hexamethylene sebacamide and caprolactam.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Birds (AREA)
- Pharmacology & Pharmacy (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21854662A | 1962-08-22 | 1962-08-22 | |
US50421865A | 1965-10-23 | 1965-10-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3427277A true US3427277A (en) | 1969-02-11 |
Family
ID=26913022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US504218A Expired - Lifetime US3427277A (en) | 1962-08-22 | 1965-10-23 | Method of making pressure-sensitive liquid-dispensing device from polyamides and article therefrom |
Country Status (3)
Country | Link |
---|---|
US (1) | US3427277A (enrdf_load_stackoverflow) |
CH (1) | CH420222A (enrdf_load_stackoverflow) |
SE (1) | SE306941B (enrdf_load_stackoverflow) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3519577A (en) * | 1964-06-22 | 1970-07-07 | Minnesota Mining & Mfg | Method for forming elastomeric particles |
US3846367A (en) * | 1973-05-24 | 1974-11-05 | Du Pont | Mineral reinforced nylon composition with high impact strength |
US4247498A (en) * | 1976-08-30 | 1981-01-27 | Akzona Incorporated | Methods for making microporous products |
US4450126A (en) * | 1982-04-21 | 1984-05-22 | Puropore, Inc. | High strength nylon blend membranes |
US4477598A (en) * | 1982-04-21 | 1984-10-16 | Puropore, Inc. | High strength nylon blend membranes |
DE3829766A1 (de) * | 1988-09-01 | 1990-03-22 | Akzo Gmbh | Verfahren zur herstellung von membranen |
US20100326919A1 (en) * | 2008-02-19 | 2010-12-30 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Monolithic supports and methods for their production |
US20110000873A1 (en) * | 2005-05-24 | 2011-01-06 | Sven Dobler | Fragrance slurry pad |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2639278A (en) * | 1950-12-22 | 1953-05-19 | Polymer Corp | Method of preparing finely divided nylon powder |
US3022542A (en) * | 1958-08-05 | 1962-02-27 | Polymer Corp | Porous polyamide articles and process for the production thereof |
US3055297A (en) * | 1957-01-14 | 1962-09-25 | Johnson & Son Inc S C | Microporous synthetic resin material |
-
1963
- 1963-08-21 SE SE9113/63A patent/SE306941B/xx unknown
- 1963-08-22 CH CH1038163A patent/CH420222A/fr unknown
-
1965
- 1965-10-23 US US504218A patent/US3427277A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2639278A (en) * | 1950-12-22 | 1953-05-19 | Polymer Corp | Method of preparing finely divided nylon powder |
US3055297A (en) * | 1957-01-14 | 1962-09-25 | Johnson & Son Inc S C | Microporous synthetic resin material |
US3022542A (en) * | 1958-08-05 | 1962-02-27 | Polymer Corp | Porous polyamide articles and process for the production thereof |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3519577A (en) * | 1964-06-22 | 1970-07-07 | Minnesota Mining & Mfg | Method for forming elastomeric particles |
US3846367A (en) * | 1973-05-24 | 1974-11-05 | Du Pont | Mineral reinforced nylon composition with high impact strength |
US4247498A (en) * | 1976-08-30 | 1981-01-27 | Akzona Incorporated | Methods for making microporous products |
US4450126A (en) * | 1982-04-21 | 1984-05-22 | Puropore, Inc. | High strength nylon blend membranes |
US4477598A (en) * | 1982-04-21 | 1984-10-16 | Puropore, Inc. | High strength nylon blend membranes |
DE3829766A1 (de) * | 1988-09-01 | 1990-03-22 | Akzo Gmbh | Verfahren zur herstellung von membranen |
US20110000873A1 (en) * | 2005-05-24 | 2011-01-06 | Sven Dobler | Fragrance slurry pad |
US20100326919A1 (en) * | 2008-02-19 | 2010-12-30 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Monolithic supports and methods for their production |
US8535527B2 (en) | 2008-02-19 | 2013-09-17 | Merck Patent Gmbh | Monolithic supports and methods for their production |
Also Published As
Publication number | Publication date |
---|---|
CH420222A (fr) | 1966-09-15 |
SE306941B (enrdf_load_stackoverflow) | 1968-12-16 |
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