EP0605446A1 - Procedure for synthesis of a white or light-coloured cross-linked halogen containing polymer - Google Patents
Procedure for synthesis of a white or light-coloured cross-linked halogen containing polymerInfo
- Publication number
- EP0605446A1 EP0605446A1 EP92918039A EP92918039A EP0605446A1 EP 0605446 A1 EP0605446 A1 EP 0605446A1 EP 92918039 A EP92918039 A EP 92918039A EP 92918039 A EP92918039 A EP 92918039A EP 0605446 A1 EP0605446 A1 EP 0605446A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- halogen containing
- glycidyl
- polymer
- cross
- 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.)
- Withdrawn
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 41
- 229910052736 halogen Inorganic materials 0.000 title claims abstract description 25
- 150000002367 halogens Chemical class 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims abstract description 20
- 230000015572 biosynthetic process Effects 0.000 title abstract description 6
- 238000003786 synthesis reaction Methods 0.000 title abstract description 4
- 239000003822 epoxy resin Substances 0.000 claims abstract description 21
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 21
- 238000004132 cross linking Methods 0.000 claims abstract description 18
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003381 stabilizer Substances 0.000 claims abstract description 15
- 239000000314 lubricant Substances 0.000 claims abstract description 5
- 239000004014 plasticizer Substances 0.000 claims abstract description 4
- 229920006037 cross link polymer Polymers 0.000 claims abstract 2
- 229920001577 copolymer Polymers 0.000 claims description 10
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- -1 glycidyl ester Chemical class 0.000 claims description 3
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 3
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000007792 addition Methods 0.000 description 12
- 239000004593 Epoxy Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 238000004458 analytical method Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000001282 organosilanes Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 2
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 150000004819 silanols Chemical class 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OWMNWOXJAXJCJI-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxymethyl)oxirane;phenol Chemical compound OC1=CC=CC=C1.OC1=CC=CC=C1.C1OC1COCC1CO1 OWMNWOXJAXJCJI-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- 239000004971 Cross linker Substances 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
- 239000004605 External Lubricant Substances 0.000 description 1
- 229910000003 Lead carbonate Inorganic materials 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 229910003849 O-Si Inorganic materials 0.000 description 1
- 229910003872 O—Si Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 description 1
- SJOCPYUKFOTDAN-ZSOIEALJSA-N methyl (4z)-4-hydroxyimino-6,6-dimethyl-3-methylsulfanyl-5,7-dihydro-2-benzothiophene-1-carboxylate Chemical compound C1C(C)(C)C\C(=N\O)C=2C1=C(C(=O)OC)SC=2SC SJOCPYUKFOTDAN-ZSOIEALJSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical class C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- QRCJOCOSPZMDJY-UHFFFAOYSA-N valnoctamide Chemical compound CCC(C)C(CC)C(N)=O QRCJOCOSPZMDJY-UHFFFAOYSA-N 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
Definitions
- the present invention concerns white or light-coloured thermostable cross-linked halogen containing polymers and a procedure for producing them.
- organosilanes are used as cross-linkers.
- the patent application DE 3719151 describes the use of organosilanes, especially mercaptosilanes (e.g. mercaptopropyl trimethoxysilane (I)) as cross-linking agents for halogen containing polymers, especially the homopolyroer PVC.
- the cross-linking is done as follows:
- First trimethoxysilane (I) is grafted on to the polymer chain, and this should preferably be done by a normal process such as compounding, extrusion or rolling.
- the cross-linking reaction is then carried out in two steps: By hot water or steam treatment alkoxysilanes are hydrolysed and form silanols. Once the silanols have been formed they quickly react with one another and form the cross link through condensation of H 2 O:
- halogen containing polymers consist of copolymers of halogen containing monomer and glycidyl acrylates.
- the preferred copolymers are copolymers between vinyl chloride monomer (VCM) and glycidyl methacrylate (GMA).
- VCM vinyl chloride monomer
- GMA glycidyl methacrylate
- the Norwegian patent application first and foremost differs from DE 3719151 in that the epoxy group introduced by the glycidyl monomers facilitates the grafting of the organosilanes to the polymer chain.
- the dominant grafting reaction is assumed to take place as follows, where a copolymer of VCM and 0.05-10% of glycidyl methacrylate are used together with (I):
- the colouring limits the usefulness of this cross-linking technique, since even after the addition of large quantities of the white pigment titanium oxide there is still a yellowish tone. This means that the cross-linking method cannot be used when whiteness is an important requirement.
- the colour is moreover unstable, showing a tendency to change under the influence of sunlight, for example. It is also difficult to add other colours, especially light colours.
- the object of the invention is thus to avoid the disadvantages of the methods described above and to obtain a cross-linked halogen containing polymer with a white or light colour.
- a further objective is to strengthen the network.
- the present invention concerns a method of producing white or light-coloured thermostable cross-linked halogen containing polymer. Surprisingly, it was found that this polymer can be produced using mercaptosilane, lead stabilizer and a low- molecular epoxy compound. The low-molecular epoxy compound reacts with the mercaptosilane and/or the by-products which together with the lead stabilizer cause the colouring, and thus remedies the problem.
- the polymer consists of 30-98 weight % halogen containing polymer, 0-60 weight % plasticizer, 0.05-10 weight % hydrolysable mercaptosilane, 0.1-10 weight % lead stabilizer, 0-4 weight % lubricant and 0.1-10 weight % epoxy resin.
- the halogen containing polymer may be a homopolymer like PVC, or a copolymer based on halogen containing polymer and inactive or reactive comonomers with respect to the cross-linking.
- a copolymer between a halogen containing monomer and a glycidyl- containing acrylate is favoured.
- the content of glycidyl- containing acrylate is 0.05-10 weight %. Under 0.05 weight % the effect is too weak and over 10% the polymerization is too slow.
- the mercaptosilane is of the general formula:
- R' a -CH 2 - -C 2 H 4 - up to C 8 H 16 or another non-functional group.
- R'' a freely selected, non-hydrolysable group
- Y one or more hydrolysable groups such as -OCH 3 , -OC 2 H 5 ,
- the compound R" can be a freely selected non-hydrolysable group.
- Examples of usable groups are -CH 2 - up to C 8 H 17 , but the choice of groups in principle has no significance for the result.
- the lead stabilizer is a freely selected commercial stabilizer based on e.g. tribasic lead sulphate, tetrabasic lead sulphate, dibasic lead phosphite, dibasic lead carbonate, dibasic lead phthalate.or dibasic lead stearate.
- the upper limit is fixed according to whatever is practical, there is no level that cannot be exceeded.
- the disadvantages of high additions are more expense and higher density.
- a practical limit is 10 weight %.
- the low-molecular epoxy compound may consist of e.g. monofunc- tional or multifunctional glycidyl ethers, glycidyl esters, glycidyl amines, or of a linear or cycloaliphatic type. This is added at 0.1-10 weight %. An addition of less than 0.1% has no effect and an addition over 10% produces too great a surplus of epoxy resin in proportion to the mercaptosilane. In addition the mixture may contain small quantities of the ordinary additives used for this type of product.
- DGEBA resin commercial epoxy resin of diglycidyl ether-bisphenol A type, known as DGEBA resin.
- Hot-set Measured as the deformation caused by a load of 0.1 MPa on a sample rod at 200° C after 15 mins., and as the residual deformation 5 mins. after the load has been removed from the sample.
- Example 3 shows that it is possible to produce white material which is strongly cross-linked by adding a low-molecular epoxy compound to the already familiar reaction between mercaptosilane, epoxy-containing halogen containing comonomer and lead stabilizer.
- the fact that the gel content decreases through addition of epoxy resin and that the deformation by heat also becomes greater is very probably a function of the fact that the low-molecular epoxy compound "steals" mercaptosilane from the epoxy- groups bonded in the chain.
- hydrolysed and condensed compounds of type (IV) have a positive effect on the hot-set, but it is no less effective than if (I) were grafted to the polymer chains.
- Example 4 shows that an increase of the amount of epoxy in the polymer chains can produce a white material with lower low- molecular epoxy resin content.
- the example shows the same tendency as Example 3, inasmuch as addition of epoxy resin decreases the gel content and increases the hot-set deformation.
- Cycloaliphatic epoxy resins are considered less reactive with mercaptan groups than for example diglycidyl ether-based epoxy resins like those of the DGEBA type.
- the higher gel content and the lower deformation than when DGEBA resin is used may be due to the fact that the cycloaliphatic epoxy resin does not compete as well with the polymer-based epoxy groups for (I).
- Example 3-5 the addition of low-molecular epoxy resin has produced a lighter or white material at the expense of a rather poorer cross-linking.
- the epoxy resin in all these experiments has been difunctional, and the mercaptosilane has been tetra- functional. This has clearly not been sufficient to make an overall positive contribution to the mechanical durability of the network in terms of hot-set values.
- Example 6 the addition of low-molecular epoxy resin has produced a lighter or white material at the expense of a rather poorer cross-linking.
- the epoxy resin in all these experiments has been difunctional, and the mercaptosilane has been tetra- functional. This has clearly not been sufficient to make an overall positive contribution to the mechanical durability of the network in terms of hot-set values.
- Example 6 Example 6 :
- Example 6 shows that the use of a tetrafunctional resin makes a contribution to the mechanical durability of the network, at least with additions of small quantities.
- the fact that the material turns light yellow is presumably due to the fact that Araldit 0163 itself is an intense yellow colour.
- the lower gel content than in Example 3 can be explained by the fact that the epoxy content is higher per weight unit in the tetrafunctional resin than in the DGEBA resin.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Procédé de synthèse d'un polymère réticulé blanc ou à coloration claire contenant un halogène polymère réticulé blanc ou à coloration claire et procédé de synthèse dudit polymère. Le polymère est constitué par 30-98 % en poids d'un polymère contenant un halogène, par 0-60 % en poids d'un plastifiant, par 0,05-10 % en poids d'un mercaptosilane hydrolysable, par 0,1-10 % en poids d'un stabilisant en plomb, par 0-4 % en poids d'un lubrifiant et par 0,1-10 % en poids d'une résine époxy. La réticulation s'effectue en présence d'humidité après le traitement du polymère.Process for the synthesis of a white or light colored crosslinked polymer containing a white or light colored crosslinked polymeric halogen and process for the synthesis of said polymer. The polymer consists of 30-98% by weight of a halogen-containing polymer, by 0-60% by weight of a plasticizer, by 0.05-10% by weight of a hydrolyzable mercaptosilane, by 0.1 -10% by weight of a lead stabilizer, by 0-4% by weight of a lubricant and by 0.1-10% by weight of an epoxy resin. Crosslinking takes place in the presence of moisture after treatment of the polymer.
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NO913441A NO173337C (en) | 1991-09-03 | 1991-09-03 | White or light colored crosslinked halogenated polymeric material and its preparation |
NO913441 | 1991-09-03 | ||
PCT/NO1992/000131 WO1993005112A1 (en) | 1991-09-03 | 1992-08-17 | Procedure for synthesis of a white or light-coloured cross-linked halogen containing polymer |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0605446A1 true EP0605446A1 (en) | 1994-07-13 |
Family
ID=19894424
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92918039A Withdrawn EP0605446A1 (en) | 1991-09-03 | 1992-08-17 | Procedure for synthesis of a white or light-coloured cross-linked halogen containing polymer |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0605446A1 (en) |
JP (1) | JP2631036B2 (en) |
KR (1) | KR940702205A (en) |
CN (1) | CN1036401C (en) |
AU (1) | AU666494B2 (en) |
BR (1) | BR9206453A (en) |
CA (1) | CA2116861A1 (en) |
FI (1) | FI940996A (en) |
HU (1) | HUT68670A (en) |
NO (1) | NO173337C (en) |
PT (1) | PT100835A (en) |
TW (1) | TW254959B (en) |
WO (1) | WO1993005112A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004051353A1 (en) * | 2004-10-21 | 2006-04-27 | Wacker Polymer Systems Gmbh & Co. Kg | Silane-modified polyvinyl alcohols |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1339497C (en) * | 1988-06-10 | 1997-10-14 | Owens-Illinois Closure Inc. | Closure assembly and method of making same using epoxidized natural oil in a low fusing, curable plastisol |
NO166189C (en) * | 1989-02-08 | 1991-06-12 | Norsk Hydro As | CIRCULATED THERMOSTABLE POLYMER AND MANUFACTURING THEREOF. |
CN1045218A (en) * | 1989-03-02 | 1990-09-12 | 合肥四达应用化学研究所 | Chinese toon juice beverage preparation and extraction technology for Chinese toon juice |
BE1005674A3 (en) * | 1991-02-20 | 1993-12-14 | Solvay | Compositions chloride copolymers vinylidene heat stabilized and use. |
-
1991
- 1991-09-03 NO NO913441A patent/NO173337C/en unknown
-
1992
- 1992-08-17 EP EP92918039A patent/EP0605446A1/en not_active Withdrawn
- 1992-08-17 KR KR1019940700698A patent/KR940702205A/en active IP Right Grant
- 1992-08-17 WO PCT/NO1992/000131 patent/WO1993005112A1/en not_active Application Discontinuation
- 1992-08-17 AU AU24749/92A patent/AU666494B2/en not_active Ceased
- 1992-08-17 HU HU9400643A patent/HUT68670A/en unknown
- 1992-08-17 CA CA002116861A patent/CA2116861A1/en not_active Abandoned
- 1992-08-17 JP JP5505119A patent/JP2631036B2/en not_active Expired - Lifetime
- 1992-08-17 BR BR9206453A patent/BR9206453A/en not_active Application Discontinuation
- 1992-09-03 CN CN92110104A patent/CN1036401C/en not_active Expired - Fee Related
- 1992-09-03 PT PT100835A patent/PT100835A/en not_active Application Discontinuation
- 1992-09-04 TW TW081107013A patent/TW254959B/zh active
-
1994
- 1994-03-02 FI FI940996A patent/FI940996A/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9305112A1 * |
Also Published As
Publication number | Publication date |
---|---|
CN1070661A (en) | 1993-04-07 |
NO913441D0 (en) | 1991-09-03 |
KR940702205A (en) | 1994-07-28 |
AU666494B2 (en) | 1996-02-15 |
HUT68670A (en) | 1995-07-28 |
BR9206453A (en) | 1995-03-01 |
PT100835A (en) | 1993-10-29 |
FI940996A0 (en) | 1994-03-02 |
NO173337C (en) | 1993-12-01 |
CA2116861A1 (en) | 1993-03-18 |
WO1993005112A1 (en) | 1993-03-18 |
TW254959B (en) | 1995-08-21 |
NO913441L (en) | 1993-03-04 |
AU2474992A (en) | 1993-04-05 |
CN1036401C (en) | 1997-11-12 |
HU9400643D0 (en) | 1994-06-28 |
FI940996A (en) | 1994-03-15 |
NO173337B (en) | 1993-08-23 |
JP2631036B2 (en) | 1997-07-16 |
JPH07500852A (en) | 1995-01-26 |
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Legal Events
Date | Code | Title | Description |
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