USRE24062E - Coated product - Google Patents
Coated product Download PDFInfo
- Publication number
- USRE24062E USRE24062E US45107954A USRE24062E US RE24062 E USRE24062 E US RE24062E US 45107954 A US45107954 A US 45107954A US RE24062 E USRE24062 E US RE24062E
- Authority
- US
- United States
- Prior art keywords
- polyethylene
- treated
- sulphuric acid
- coated product
- product
- 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
Links
- 229920000573 polyethylene Polymers 0.000 description 29
- 239000004698 Polyethylene Substances 0.000 description 26
- -1 polyethylene Polymers 0.000 description 26
- 238000000034 method Methods 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 235000011149 sulphuric acid Nutrition 0.000 description 6
- 239000001117 sulphuric acid Substances 0.000 description 6
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000976 ink Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 3
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 3
- 230000001464 adherent effect Effects 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 230000005661 hydrophobic surface Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229920001220 nitrocellulos Polymers 0.000 description 3
- 229940079938 nitrocellulose Drugs 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 229920013646 Hycar Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- MCUDGYVHPADJBD-UHFFFAOYSA-L hydroxy-(hydroxy(dioxo)chromio)oxy-dioxochromium sulfuric acid Chemical compound OS(O)(=O)=O.O[Cr](=O)(=O)O[Cr](O)(=O)=O MCUDGYVHPADJBD-UHFFFAOYSA-L 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
Definitions
- polyethylene surfaces readily may be made hydrophilic and adaptable to cementing and printing by oxidation with a strong sulphuric acid-dichromate solution which may be obtained by saturating concentrated sulphuric acid with technical sodium dichromate.
- the surface is prepared simply by passing it through a bath of the oxidizing solution and then washing in water and drying.
- the surface treatment of the present invention may be integrated in the continuous production so as continuously to produce a1product having a hydrophilic surface.
- the degree of treatment or modification of the normally hydrophobic surface can be regulated by varying the temperature and strength of the acid-dichromate solution and the exposure time of the surface to the'solution.
- a treated surface can be printed on quite successfully with nitro cellulose lacquer. If the printed surface is submerged in water for an hour, the printing can be scratched off, but will not be damaged by rubbing.
- the treatment does not inpair the optical properties 7 of the sheet and, in fact, has been found to improve considerably the transparency or clarity of polyethylene.
- Metals may be easily deposited on such treated surfaces by allowing the surface to come into contact with an aqueous solution of a readily-reducible metal salt and reducing the metallic salt. Thin films of copper and silvermay be deposited in this manner. Metals may also be applied to the treated surface by the process of low vacuum volatilisation. Better adhesion is obtained when the metals are applied to treated, as compared with untreated, polyethylene surfaces.
- the polyethylene treatment of the present invention maybe used wherever the hydrophilic property is required or helpful.
- the interior of polyethylene bottles treated with the aciddichromate has been, successfully given an adherent chain as a result of the sulphuric acid-dichromate treatment. Water is found to spread evenly over a polyethylene surface treated in this way instead of gathering in drops as in the case of an untreated surface. Subsequent exposure of a treated surface to water does not wash away or destroy the hydrophilic character of the treated surface.
- the treated surface will take up basic dyes from an aqueous solution, while adhesives and cements based on polyvinyl alcohol, polyvinyl acetate, nitro cellulose, gelatin, Hycar rubber and similar polar compounds adhere readily to such a surface.
- Hycar rubber is the name given by B. F. Goodrich Company to a synthetic rubber compound that is a butadiene copolymer of undisclosed composition. Solvents which migrate readily through polyethylene as, for example, methyl ethyl ketone, can be used as solvents for the cement.
- electrostatic charges do not accumulate on polyethylene surfaces treated according to the process of the present invention and polyethylene thus treated can advantageously be used in-the manufacture of covers, for instruments, dials, gauges, indicators and the like, especially those in which accumulation of electrostatic charges on the cover has a disturbing influence on the instrument itself.
- the process of treating polyethylene products which comprises exposing the product to a saturated solution of sodium dichromate in concentrated sulphuric acid to render the surface of the polyethylene hydrophilic, receptive to printing ink, and free of static electricity.
- Solid polyethylene having a surface which is bydrophilic, receptive to printing inks, and free of static charge, said surface comprising essentially oxdired polyme and which surface has an adherent film of an oil I 2,413,789 Seheiderbauer Jan. 7, 1947 resistant polar compound. v 2,418,018 Erusberger et a1 Mar. 25, 1947 II.
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Printing Plates And Materials Therefor (AREA)
Description
orlglna'lpatentliutformsnopartof madehyrelnue.
J 4 United States Pam Ofiice Re. 24,062 Reissuecl Sept. 30,. 1955 PROCESS FOR TREATING POLYETIIYLENE AND COATED PRODUCT Pllll V. [ml] P I" N. Y J to M p mihiflommssotnenware,
No Drawing. Original No. 2,668,134, dated February 2,
1954, Serlal No. 47,147, August 31, 1948. guru for reimue August 19, 1954, Serial No. 451,
11 Claims. (Cl. 154-439) Matter enclosed in heavy brackets 1 h the liw specllicatlon; matter printed in Italics indicates the additions V This invention relates to the preparation of polyethylene Q articles for cementing or printing, and more particularly tinto the oxidation of the normally hydrophobic surfaces of the articles so that they are hypophilic and free of static charge.
Heretofore, difliculty has been experienced in cementing polyethylene products and in printing legends thereon, the normally hydrophobic surface of polyethylene being unreceptive to most glues, adhesives and printing inks and dyes.
in accordance with the present invention, polyethylene surfaces readily may be made hydrophilic and adaptable to cementing and printing by oxidation with a strong sulphuric acid-dichromate solution which may be obtained by saturating concentrated sulphuric acid with technical sodium dichromate. The surface is prepared simply by passing it through a bath of the oxidizing solution and then washing in water and drying.
In the case of polyethylene sheet and similar products which are formed by continuous processes, as for example, extrusion, the surface treatment of the present invention may be integrated in the continuous production so as continuously to produce a1product having a hydrophilic surface.
The degree of treatment or modification of the normally hydrophobic surface can be regulated by varying the temperature and strength of the acid-dichromate solution and the exposure time of the surface to the'solution.
' With strong solution at room temperature (70 F.) the treatment is practically instantaneousin rendering the surface hydrophilic.
, The subsequent washing of the treated surface immediately and completely removes any sulphuric acid products which may have adhered to the polyethylene 2 way it is possible to form letters and other drapes on polyethylene by subjecting such treated areas to the action of dyes or aqueous inks. A treated surface can be printed on quite successfully with nitro cellulose lacquer. If the printed surface is submerged in water for an hour, the printing can be scratched off, but will not be damaged by rubbing.
The treatment does not inpair the optical properties 7 of the sheet and, in fact, has been found to improve considerably the transparency or clarity of polyethylene.
Metals may be easily deposited on such treated surfaces by allowing the surface to come into contact with an aqueous solution of a readily-reducible metal salt and reducing the metallic salt. Thin films of copper and silvermay be deposited in this manner. Metals may also be applied to the treated surface by the process of low vacuum volatilisation. Better adhesion is obtained when the metals are applied to treated, as compared with untreated, polyethylene surfaces.
It will be-understood that the polyethylene treatment of the present invention maybe used wherever the hydrophilic property is required or helpful. For example, the interior of polyethylene bottles treated with the aciddichromate has been, successfully given an adherent chain as a result of the sulphuric acid-dichromate treatment. Water is found to spread evenly over a polyethylene surface treated in this way instead of gathering in drops as in the case of an untreated surface. Subsequent exposure of a treated surface to water does not wash away or destroy the hydrophilic character of the treated surface. The treated surface will take up basic dyes from an aqueous solution, while adhesives and cements based on polyvinyl alcohol, polyvinyl acetate, nitro cellulose, gelatin, Hycar rubber and similar polar compounds adhere readily to such a surface. Hycar rubber is the name given by B. F. Goodrich Company to a synthetic rubber compound that is a butadiene copolymer of undisclosed composition. Solvents which migrate readily through polyethylene as, for example, methyl ethyl ketone, can be used as solvents for the cement.
It will be obvious that the whole of the surface of the polyethylene article need not be treated with the aciddichrornate but that areasofvarious disposer form canbesubiectedtotheactionofthesolution. Inthis oil resistant film of polyvinyl alcohol. It was found that the adherence of the him was great enough to tear the surface of the polyethylene. I
It also has been found that electrostatic charges do not accumulate on polyethylene surfaces treated according to the process of the present invention and polyethylene thus treated can advantageously be used in-the manufacture of covers, for instruments, dials, gauges, indicators and the like, especially those in which accumulation of electrostatic charges on the cover has a disturbing influence on the instrument itself.
I claim:
l. The process of treating polyethylene products which comprises exposing the product to a saturated solution of sodium dichromate in concentrated sulphuric acid to render the surface of the polyethylene hydrophilic, receptive to printing ink, and free of static electricity.
2. The process of treating polyethylene products which.
comprises exposing the product to a bath of sulphuric acid and sodium dichromate, washing the product in water and drying. 1
3. The process recited in claim 2 wherein the product is exposed only instantaneously to the acid-dichromate.
4. The process recited in claim 2 and including exposing the product to a dye.
5. The process of treating polyethylene products which comprises exposing the product to a bath of sulphuric acid and sodium dichromate, washing, drying, applying a nitro cellulose lacquer.
6. The process of bonding a polyethylene surface to another surface which comprises exposing the polyethylene surface to a bath of sulphuric acid and sodium dichromate, washing, and bonding the surfaces together with a polar cement.
7. Solid polyethylene having a surface which is bydrophilic, receptive to printing inks, and free of static charge, said surface comprising essentially oxdired polyme and which surface has an adherent film of an oil I 2,413,789 Seheiderbauer Jan. 7, 1947 resistant polar compound. v 2,418,018 Erusberger et a1 Mar. 25, 1947 II. A polyethylene article, a surface of which com- 2,431,042 I ngersoll Nov. 18, 1947 1" I prises polar compound receptive; oxidized polyethylene 2,431,956 Moody Dec. 2, 1947 1 and which surface has an adherent film of an oil re 5 2,446,536 Hardy Aug. 10, 1948 i sis-tan: polar compound. 2,584,722 London Feb. 5, 1952 References Cited in the file of, this patent OTHER REFERENCES 7 orthe original patent British Plastics, Properties and Uses of Polythene,"
- 1 Richards, April 1945, pp. 146 to 151.
v UNITED STATES PATENTS Modern Inorganic Chemistry," Mellor, 1917, p. 465. g v 2,125-374 Herman al B- 2, 1938 Industrial and Engineering Chem, Polythene, June 3 2,153,553 Fawcet et al Apr. 11, 1939 7 1945 pp. 52541 1315-196. Schlack Sepl- 1940 :British Plastics, Properties and Uses of Polythene, 2,341,885 Feb-15,1944 15 Midwinter, May 1945, pp. 208-228. 7
2,400,720 S tandinger et a1; May 21, 1946
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45107954 USRE24062E (en) | 1948-08-31 | 1954-08-19 | Coated product |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47147A US2668134A (en) | 1948-08-31 | 1948-08-31 | Process for treating polyethylene and coated product |
| US45107954 USRE24062E (en) | 1948-08-31 | 1954-08-19 | Coated product |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE24062E true USRE24062E (en) | 1955-09-20 |
Family
ID=29218136
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US45107954 Expired USRE24062E (en) | 1948-08-31 | 1954-08-19 | Coated product |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE24062E (en) |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2828237A (en) * | 1955-09-08 | 1958-03-25 | American Viscose Corp | Sealing polyethylene to other organic resins |
| US2832699A (en) * | 1956-04-30 | 1958-04-29 | Dow Chemical Co | Method for destaticizing polyethylene and articles thereby obtained |
| US2832698A (en) * | 1956-04-30 | 1958-04-29 | Dow Chemical Co | Method for destaticizing polymeric substances and articles thereby obtained |
| US2937066A (en) * | 1955-11-23 | 1960-05-17 | Dow Chemical Co | Method for treating polyethylene and treated polyethylene articles thereby obtained |
| US2955970A (en) * | 1957-10-25 | 1960-10-11 | Lowe Paper Co | Extrusion coating |
| US2973241A (en) * | 1956-10-26 | 1961-02-28 | Phillips Petroleum Co | Method for producing high crystalline 1-olefin polymers of decreased flammability by treatment with nitric acid and resulting products |
| US2991217A (en) * | 1956-11-13 | 1961-07-04 | American Can Co | Method for improving the wettability of polyethylene by aqueous compositions |
| US3035915A (en) * | 1958-12-29 | 1962-05-22 | Du Pont | Process for rendering polyester film receptive to photographic materials and resulting elements |
| US3043818A (en) * | 1959-03-20 | 1962-07-10 | Du Pont | Polymeric compositions |
| US3067949A (en) * | 1959-07-22 | 1962-12-11 | Gen Motors Corp | Electrostatic coating apparatus with rotary impeller |
| US3091536A (en) * | 1956-08-02 | 1963-05-28 | Montedison Spa | Photographic films comprising a synthetic resin support |
| US3099350A (en) * | 1959-12-14 | 1963-07-30 | Nat Distillers Chem Corp | Packaging films and package produced therefrom |
| US3101989A (en) * | 1959-07-09 | 1963-08-27 | Rhodiaceta | Process for improving the affinity for dyes of shaped polyolefine articles |
| US3112199A (en) * | 1958-01-28 | 1963-11-26 | Montedison Spa | Laminates including photographic films comprising modified, superficially adhesive films of crystalline polymeric alpha-olefins, and methods for making such laminates |
| US3231454A (en) * | 1961-04-14 | 1966-01-25 | Cadillac Products | Cushioning material |
| US3248271A (en) * | 1961-05-08 | 1966-04-26 | Celanese Corp | Shaped oxymethylene thermoplastic polymer and method of surface treating same |
| US3256365A (en) * | 1956-06-20 | 1966-06-14 | Du Pont | Composition comprising polyethylene and oxidation products of polyethylene and articles thereof |
| US3282729A (en) * | 1963-02-27 | 1966-11-01 | Union Carbide Corp | Barrier coated thermoplastic olefin polymer substrates |
| US3306791A (en) * | 1962-10-08 | 1967-02-28 | Gulton Ind Inc | Bonding of epoxy resins to polyolefin plastic materials |
| US3317330A (en) * | 1965-01-05 | 1967-05-02 | Chemclean Corp | Method of treating polyethylene and polypropylene plastic surfaces |
| US3412178A (en) * | 1964-04-16 | 1968-11-19 | Gulf Oil Corp | Ethylene copolymer |
| US4055695A (en) | 1970-01-30 | 1977-10-25 | Imperial Chemical Industries Limited | Foamed polyolefine films |
| US4421780A (en) | 1980-12-24 | 1983-12-20 | Societa' Italiana Resine S.I.R. S.P.A. | Heat-sealable polyolefin films and processes for their preparation |
| US4515210A (en) | 1981-01-15 | 1985-05-07 | Courtaulds Plc | Heat exchanger having a plastics membrane |
-
1954
- 1954-08-19 US US45107954 patent/USRE24062E/en not_active Expired
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2828237A (en) * | 1955-09-08 | 1958-03-25 | American Viscose Corp | Sealing polyethylene to other organic resins |
| US2937066A (en) * | 1955-11-23 | 1960-05-17 | Dow Chemical Co | Method for treating polyethylene and treated polyethylene articles thereby obtained |
| US2832699A (en) * | 1956-04-30 | 1958-04-29 | Dow Chemical Co | Method for destaticizing polyethylene and articles thereby obtained |
| US2832698A (en) * | 1956-04-30 | 1958-04-29 | Dow Chemical Co | Method for destaticizing polymeric substances and articles thereby obtained |
| US3256365A (en) * | 1956-06-20 | 1966-06-14 | Du Pont | Composition comprising polyethylene and oxidation products of polyethylene and articles thereof |
| US3091536A (en) * | 1956-08-02 | 1963-05-28 | Montedison Spa | Photographic films comprising a synthetic resin support |
| US2973241A (en) * | 1956-10-26 | 1961-02-28 | Phillips Petroleum Co | Method for producing high crystalline 1-olefin polymers of decreased flammability by treatment with nitric acid and resulting products |
| US2991217A (en) * | 1956-11-13 | 1961-07-04 | American Can Co | Method for improving the wettability of polyethylene by aqueous compositions |
| US2955970A (en) * | 1957-10-25 | 1960-10-11 | Lowe Paper Co | Extrusion coating |
| US3112199A (en) * | 1958-01-28 | 1963-11-26 | Montedison Spa | Laminates including photographic films comprising modified, superficially adhesive films of crystalline polymeric alpha-olefins, and methods for making such laminates |
| US3035915A (en) * | 1958-12-29 | 1962-05-22 | Du Pont | Process for rendering polyester film receptive to photographic materials and resulting elements |
| US3043818A (en) * | 1959-03-20 | 1962-07-10 | Du Pont | Polymeric compositions |
| US3101989A (en) * | 1959-07-09 | 1963-08-27 | Rhodiaceta | Process for improving the affinity for dyes of shaped polyolefine articles |
| US3067949A (en) * | 1959-07-22 | 1962-12-11 | Gen Motors Corp | Electrostatic coating apparatus with rotary impeller |
| US3099350A (en) * | 1959-12-14 | 1963-07-30 | Nat Distillers Chem Corp | Packaging films and package produced therefrom |
| US3231454A (en) * | 1961-04-14 | 1966-01-25 | Cadillac Products | Cushioning material |
| US3248271A (en) * | 1961-05-08 | 1966-04-26 | Celanese Corp | Shaped oxymethylene thermoplastic polymer and method of surface treating same |
| US3306791A (en) * | 1962-10-08 | 1967-02-28 | Gulton Ind Inc | Bonding of epoxy resins to polyolefin plastic materials |
| US3282729A (en) * | 1963-02-27 | 1966-11-01 | Union Carbide Corp | Barrier coated thermoplastic olefin polymer substrates |
| US3412178A (en) * | 1964-04-16 | 1968-11-19 | Gulf Oil Corp | Ethylene copolymer |
| US3317330A (en) * | 1965-01-05 | 1967-05-02 | Chemclean Corp | Method of treating polyethylene and polypropylene plastic surfaces |
| US4055695A (en) | 1970-01-30 | 1977-10-25 | Imperial Chemical Industries Limited | Foamed polyolefine films |
| US4421780A (en) | 1980-12-24 | 1983-12-20 | Societa' Italiana Resine S.I.R. S.P.A. | Heat-sealable polyolefin films and processes for their preparation |
| US4515210A (en) | 1981-01-15 | 1985-05-07 | Courtaulds Plc | Heat exchanger having a plastics membrane |
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