WO1992020728A1 - Method for producing an ionomer - Google Patents
Method for producing an ionomer Download PDFInfo
- Publication number
- WO1992020728A1 WO1992020728A1 PCT/NL1992/000086 NL9200086W WO9220728A1 WO 1992020728 A1 WO1992020728 A1 WO 1992020728A1 NL 9200086 W NL9200086 W NL 9200086W WO 9220728 A1 WO9220728 A1 WO 9220728A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- plastic
- conducting medium
- medium
- electrical field
- elec
- Prior art date
Links
- 229920000554 ionomer Polymers 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 239000004033 plastic Substances 0.000 claims abstract description 51
- 229920003023 plastic Polymers 0.000 claims abstract description 51
- 230000005684 electric field Effects 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 9
- -1 polyethylene Polymers 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000344 soap Substances 0.000 claims description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000005192 partition Methods 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 238000009740 moulding (composite fabrication) Methods 0.000 description 6
- 125000000524 functional group Chemical group 0.000 description 5
- 150000002500 ions Chemical group 0.000 description 4
- 229910021645 metal ion Inorganic materials 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000010416 ion conductor Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 235000010269 sulphur dioxide Nutrition 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0093—Chemical modification
- B01D67/00931—Chemical modification by introduction of specific groups after membrane formation, e.g. by grafting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/0081—After-treatment of articles without altering their shape; Apparatus therefor using an electric field, e.g. for electrostatic charging
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
- H01M6/181—Cells with non-aqueous electrolyte with solid electrolyte with polymeric electrolytes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2096/00—Use of specified macromolecular materials not provided for in a single one of main groups B29K2001/00 - B29K2095/00, as moulding material
- B29K2096/005—Ionomers
Definitions
- the invention relates to a method for producing an ionomer.
- the invention relates more in particular to the producing of an ionomer from a plastic which initially usual ⁇ ly contains no incorporated ion compounds in addition to the normal organic covalent bonds.
- This new method for producing ionomers comprises of: i) providing a plastic; ii) placing an electrically conducting medium in contact with a plastic surface of the plastic; and iii) applying an electrical field over the plastic surface. It has been found, namely, that if a plastic is loaded with an electrical field in the presence of an electrically conducting medium, groups are radicalized or ionized from the external and/or internal plastic surface in the direction of the electrical field in the plastic, which groups are con ⁇ verted as a result for instance of oxidation reactions into for example carboxylic acids and/or sulphonic acids. Under ⁇ stood by plastic surface is, among other things, an external plastic surface optionally provided with grooves, scratches or other surface defects and walls of cavities in the plastic which may contain contaminants.
- hydrophilic channels which are however se i- p rmeable.
- the electrically conducting medium for instance water, is mobile in these channels but hydrated ions can only displace in these channels under the influence of the elec- trical field.
- an ionomer according to the invention can also be provided with cavities in which salts are entrapped. Both liquids and gases can be used as electrically conducting medium.
- the latter has the particular objective that the oxidized groups can dissociate and form an ionoge- nic, functional group with the metal ions supplied by the medium.
- the electrically conducting medium can be an inorga ⁇ nic medium such as water and ammonia.
- the electrically con ⁇ ducting medium can likewise be an organic medium such as alkanols, for instance methanol and ethanol. If the electri ⁇ cally conducting medium has an inherent insufficient activi- ty, diverse reactive components can be added to the medium and/or to the plastic.
- One group of reactive components consists of gases such as oxygen, ozone, sulphur oxide, for instance sulphur dioxide. Such gases can sustain and assist the radical-form- ing or ion-forming reactions as well as the oxidation reac ⁇ tions.
- gases such as oxygen, ozone, sulphur oxide, for instance sulphur dioxide.
- gases can sustain and assist the radical-form- ing or ion-forming reactions as well as the oxidation reac ⁇ tions.
- Another group of reactive components is formed by salts, particularly salts of multivalent metal ions such as copper, tin and manganese.
- salts particularly salts of multivalent metal ions such as copper, tin and manganese.
- metal ions accelerate the growth of the hydrophilic channels, possibly partly due to a catalytic acceleration of the oxidation reactions.
- Another group of reactive components is formed by surface-active substances such as a soap.
- surface-active substances for example a stearate, can on the one hand effect the same function as the salts and on the other reduce the surface tension so that the electrically conduct ⁇ ing, more or less polar medium can penetrate more rapidly into the apolar plastic.
- Other examples of soaps for use comprise alkyl sulphonates, aryl sulphonates, alkyl(aryl) sulphonates and ethylene oxide adducts optionally in combina ⁇ tion with alkyl and/or aryl groups.
- the magnitude of the electrical field applied over the plastic is not limited to a determined value.
- a first forming of ionogenic, functional groups already takes place from a value of 1 V/mm of plastic.
- An upper limit for the magnitude of the electrical field is determined by the short-circuit voltage of the plastic, which voltage can change as the iono eric character of the plastic increases.
- a reasonable speed for the forming of the ionogenic, functional groups occurs with an electrical field of 0.2 to 20 kV/mm. If for instance the plastic consists of polyethylene, optimum speeds for the forming of ionogenic, functional groups are obtained when the electrical field amounts to 0.5 to 10 kV/ m. In general, the strongest possible electrical field will be applied, having in practice a value approximately equal to half the short-circuit voltage.
- the frequency of the applied field amounts generally to 1 to 10 5 Hz, preferably 10 Hz to 25 kHz. It has been found however that the magnitude of the frequency can influence the properties of the formed ionomers. For instance at lower frequencies of 5 Hz to 10 kHz mainly electrochemical reac ⁇ tions will occur (oxidation reactions) whereby mainly hydro ⁇ philic channels are formed. At higher frequencies, for exam- pie from 100 Hz, the ion conduction phenomenon will occur to a greater extent whereby, when the electrically conducting medium contains salts, salts can penetrate into cavities inside the hydrophilic channels and possibly contribute to cavity forming. Once enclosed in these cavities and in the absence of an electrical field, these salts are irreversibly entrapped inside the ionomer.
- the ionomer produced according to the invention gene ⁇ rally has the form of a sheet.
- This sheet form may already be present in the plastic subjected to the method. It is however possible that a for example hollow cylindrical plastic is subjected to a radially oriented electrical field, whereafter an ionomer in the form of a sheet is formed from this hollow cylindrical plastic by means of delamination, optionally by peeling.
- An optimum method for producing ionomers is obtained if the plastic is placed in contact with the conducting medium on surfaces facing away from each other.
- a preferred embodiment for performing the method according to the invention comprises the use of a strip-like plastic which is converted into a channel shape, into which channel liquid, electrically conducting medium is introduced.
- the channel-shaped plastic is guided through a bath of liquid electrically conducting medium.
- an electrode for applying the electrical field over the plastic strip.
- the plastic in this case in the form of a plastic foil, can form a parti ⁇ tion between two medium chambers each containing for instance gaseous electrically conducting medium (for instance water vapour) and an electrode for generating the electrical field. If a good sealing with the chamber walls is ensured, this method can likewise be converted into a continuous method.
- gaseous electrically conducting medium for instance water vapour
- Plastics which can be converted into ionomers with the method according to the invention are in principle not limi ⁇ ted to a specific group of plastics, plastics which can particularly be used comprise polyethylene, polypropylene, polystyrene and polytetrafluoroethylene.
- the ionomers produced in accordance with the method according to the invention can be applied in very many fie ⁇ lds.
- An example which might be quoted is as ion conductor in for instance polymer batteries, in which the ionomer func ⁇ tions as an electrolyte.
- the ionomer can also be applied as a semi-permeable membrane with a selective permeability for particular types of molecules and ions, wherein the permeabi ⁇ lity can moreover be adjusted as a function of the electrical field and/or the temperature.
- the ionomers can be used for purifying solutions, dispersions and emulsions of both chemical and medicinal nature.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Transplantation (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Electrochemistry (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Saccharide Compounds (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE69232733T DE69232733T2 (en) | 1991-05-10 | 1992-05-08 | METHOD FOR PRODUCING AN IONOMER |
DK92917395T DK0647249T3 (en) | 1991-05-10 | 1992-05-08 | Process for preparing an ionomer |
EP92917395A EP0647249B1 (en) | 1991-05-10 | 1992-05-08 | Method for producing an ionomer |
AT92917395T ATE222272T1 (en) | 1991-05-10 | 1992-05-08 | METHOD FOR PRODUCING AN IONOMER |
US08/146,076 US5427662A (en) | 1991-05-10 | 1992-05-08 | Method for producing an ionomer |
JP51016392A JP3268531B2 (en) | 1991-05-10 | 1992-05-08 | Manufacturing method of ionomer |
NO934030A NO308477B1 (en) | 1991-05-10 | 1993-11-08 | Process for preparing an ionomer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL9100815 | 1991-05-10 | ||
NL9100815A NL9100815A (en) | 1991-05-10 | 1991-05-10 | METHOD FOR MANUFACTURING AN IONOMER |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1992020728A1 true WO1992020728A1 (en) | 1992-11-26 |
Family
ID=19859237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1992/000086 WO1992020728A1 (en) | 1991-05-10 | 1992-05-08 | Method for producing an ionomer |
Country Status (12)
Country | Link |
---|---|
US (1) | US5427662A (en) |
EP (1) | EP0647249B1 (en) |
JP (1) | JP3268531B2 (en) |
AT (1) | ATE222272T1 (en) |
AU (1) | AU1874592A (en) |
CA (1) | CA2102510A1 (en) |
DE (1) | DE69232733T2 (en) |
DK (1) | DK0647249T3 (en) |
ES (1) | ES2179041T3 (en) |
NL (1) | NL9100815A (en) |
NO (1) | NO308477B1 (en) |
WO (1) | WO1992020728A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996033293A1 (en) * | 1995-04-19 | 1996-10-24 | Korea Institute Of Science And Technology | Modification of surfaces of polymers, metal or ceramic |
NL1005418C2 (en) * | 1997-03-03 | 1998-09-07 | Kema Nv | Method for treating a base material to obtain specific properties. |
WO2002031030A1 (en) * | 2000-10-12 | 2002-04-18 | Osaka Gas Co., Ltd. | Formed resin article |
EP1548447A1 (en) * | 2002-09-26 | 2005-06-29 | ARKRAY, Inc. | Method of producing analytical tool |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009026376A1 (en) | 2009-08-14 | 2011-02-24 | Karl August Dr. Brensing | Device for introducing gas into liquids |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1128644B (en) * | 1958-03-01 | 1962-04-26 | Kalle Ag | Process for modifying the surface properties of deformed thermoplastics |
US3124729A (en) * | 1957-06-04 | 1964-03-10 | Method for preparing surfaces com- | |
FR2119546A5 (en) * | 1970-12-22 | 1972-08-04 | Monsanto Chemicals | |
GB2013213A (en) * | 1978-01-26 | 1979-08-08 | Troester Gmbh | Method of cross linking plastics and/or rubber materials |
US4353799A (en) * | 1976-05-19 | 1982-10-12 | Baxter Travenol Laboratories, Inc. | Hydrophobic diffusion membranes for blood having wettable surfaces |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62263361A (en) * | 1986-05-09 | 1987-11-16 | 東レ株式会社 | Production of nonwoven fabric |
US4988419A (en) * | 1988-01-20 | 1991-01-29 | Industrial Management Co. | Method and apparatus for producing conductivity in materials |
EP0436918B1 (en) * | 1990-01-03 | 1995-06-28 | Wolff Walsrode Aktiengesellschaft | Process for treating a polyolefin film |
-
1991
- 1991-05-10 NL NL9100815A patent/NL9100815A/en unknown
-
1992
- 1992-05-08 JP JP51016392A patent/JP3268531B2/en not_active Expired - Fee Related
- 1992-05-08 EP EP92917395A patent/EP0647249B1/en not_active Expired - Lifetime
- 1992-05-08 US US08/146,076 patent/US5427662A/en not_active Expired - Fee Related
- 1992-05-08 DK DK92917395T patent/DK0647249T3/en active
- 1992-05-08 CA CA002102510A patent/CA2102510A1/en not_active Abandoned
- 1992-05-08 AT AT92917395T patent/ATE222272T1/en not_active IP Right Cessation
- 1992-05-08 DE DE69232733T patent/DE69232733T2/en not_active Expired - Fee Related
- 1992-05-08 ES ES92917395T patent/ES2179041T3/en not_active Expired - Lifetime
- 1992-05-08 WO PCT/NL1992/000086 patent/WO1992020728A1/en active IP Right Grant
- 1992-05-08 AU AU18745/92A patent/AU1874592A/en not_active Abandoned
-
1993
- 1993-11-08 NO NO934030A patent/NO308477B1/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3124729A (en) * | 1957-06-04 | 1964-03-10 | Method for preparing surfaces com- | |
DE1128644B (en) * | 1958-03-01 | 1962-04-26 | Kalle Ag | Process for modifying the surface properties of deformed thermoplastics |
FR2119546A5 (en) * | 1970-12-22 | 1972-08-04 | Monsanto Chemicals | |
US4353799A (en) * | 1976-05-19 | 1982-10-12 | Baxter Travenol Laboratories, Inc. | Hydrophobic diffusion membranes for blood having wettable surfaces |
GB2013213A (en) * | 1978-01-26 | 1979-08-08 | Troester Gmbh | Method of cross linking plastics and/or rubber materials |
Non-Patent Citations (3)
Title |
---|
CHEMICAL ABSTRACTS, , 10 December 1979, Columbus, Ohio, US; abstract no. 91-193764N, GELAZOV KERIMOV: 'THERMOLUMINESCENCE OF POLYETHYLENE CAUSED BY A STRONG ELECTRIC FIELD' * |
CHEMICAL ABSTRACTS, , 15 November 1982, Columbus, Ohio, US; abstract no. 97-163621V, GEZALOV KERIMO: 'PRE-BREAKDOWN FREE RADICAL STATES IN POLYETHYLENE' * |
CHEMICAL ABSTRACTS, , 3 July 1989, Columbus, Ohio, US; abstract no. 110-95925G, RAGIMOV MAMEDOV ABASOV ALEKPEROV: 'STRONG ELECTRICAL FIELD EFFECT ON MOLECULAR MECHANISM OF POLYETHYLENE DEGRADATION' * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996033293A1 (en) * | 1995-04-19 | 1996-10-24 | Korea Institute Of Science And Technology | Modification of surfaces of polymers, metal or ceramic |
NL1005418C2 (en) * | 1997-03-03 | 1998-09-07 | Kema Nv | Method for treating a base material to obtain specific properties. |
WO1998039092A1 (en) * | 1997-03-03 | 1998-09-11 | N.V. Kema | Method of treating a base material for obtaining specific properties |
US6342130B1 (en) | 1997-03-03 | 2002-01-29 | N.V. Kema | Method of treating a base material for obtaining specific properties |
WO2002031030A1 (en) * | 2000-10-12 | 2002-04-18 | Osaka Gas Co., Ltd. | Formed resin article |
EP1548447A1 (en) * | 2002-09-26 | 2005-06-29 | ARKRAY, Inc. | Method of producing analytical tool |
EP1548447A4 (en) * | 2002-09-26 | 2010-11-03 | Arkray Inc | Method of producing analytical tool |
Also Published As
Publication number | Publication date |
---|---|
CA2102510A1 (en) | 1992-11-11 |
NO934030D0 (en) | 1993-11-08 |
EP0647249A1 (en) | 1995-04-12 |
JP3268531B2 (en) | 2002-03-25 |
NO308477B1 (en) | 2000-09-18 |
ATE222272T1 (en) | 2002-08-15 |
US5427662A (en) | 1995-06-27 |
ES2179041T3 (en) | 2003-01-16 |
DE69232733T2 (en) | 2003-04-24 |
EP0647249B1 (en) | 2002-08-14 |
NL9100815A (en) | 1992-12-01 |
JPH06507657A (en) | 1994-09-01 |
AU1874592A (en) | 1992-12-30 |
DE69232733D1 (en) | 2002-09-19 |
NO934030L (en) | 1993-11-08 |
DK0647249T3 (en) | 2002-11-25 |
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