• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    An antimicrobial agent is described for polymers based on a 2,2,6,6-tetramethylpiperidine derivative, wherein the 2,2,6,6-tetramethylpiperidine derivative of the formula having n> 2 comprising at least two primary or secondary amino groups by means of a polyoxirane compound of the formula is converted to a polymeric compound containing the structural unit at regular intervals.
    公开号:AT510488A1
    申请号:T1622/2010
    申请日:2010-09-29
    公开日:2012-04-15
    发明作者:
    申请人:Ke Kelit Kunststoffwerk Gmbh；
    IPC主号:
    专利说明:

    -1 - ► ♦ ·
    (37 498) II
    The invention relates to an antimicrobial agent for polymers based on a 2,2,6,6-tetramethylpiperidine derivative.
    Biocides such as sulfonamides, cephalosporins, tetracyclines and the like. Like., Engage in metabolic processes typical of protozoa and must therefore generally have small-molecule structures and be water-soluble. This, however, provides the essential preconditions for an unwanted influence to be exerted on other metabolic processes, all of which take place in an aqueous environment, which should be avoided as far as possible. These disadvantages are avoided by Kontaktbiocide, which usually form high molecular weight, protonatable, chemical compounds that, without entering into aqueous solution or intervene in the internal metabolism, killing unicellular organisms by mere contact due to static charges and the resulting cell lysis. However, known contact biocides, for example polymers of basic methacrylates due to the system-immanent ester groups could not prevail, on the one hand because of the insufficient Hydroiysestabilität the ester groups and on the other hand because of the lack of compatibility of the polyester with the market dominating group of polyolefins.
    To be able to equip transparent plastics with an antimicrobial agent, without impairing the properties of the plastic, in particular with regard to transparency and weather resistance, it has already been proposed (EP 0 945 064 B1) to use 2,2,6,6-tetramethylpiperidine derivatives as antimicrobial agent , so sterically hindered amines, as they are widely used as light stabilizers for outdoor plastics. The biocidal effect is, however, comparatively low. In addition, despite good hydrolytic stability, there is a risk of flooding out of a substrate due to molecular weight.
    The invention is therefore based on the object to provide a Kontaktbiocid that can meet the demands placed on such antimicrobial agent requirements, in particular with regard to water insolubility, stability and long-term effect, beneficial.
    Starting from an antimicrobial agent of the type described above, the invention solves the stated problem by providing a 2,2,6,6-tetramethylpiperidine derivative of the formula ## STR3 ## which comprises at least two primary or secondary amino groups
    with n > 2 is converted by means of a poly-oxirane compound of the formula CH - CH-R1-CH-CH2 oo to a polymeric compound which is the structural unit
    contains at regular intervals.
    By reacting the sterically hindered amines known per se as light stabilizers for polymers, which are provided with at least two primary or secondary amino groups with difunctional reactive molecules to give high molecular weight structures, advantageous conditions for contact biocides are created because of the high molecular weight ensures a high degree of insolubility and a comparatively low, only large-meshed cross-linking is present, so that on the largely linear molecules the unicellular organisms, such as Gram-positive and Gram-negative bacteria, molds and the like, can dock to the cationically active groups without being hindered become. As a result of the charge exchange with the lipoproteins of the bacterial cell envelope, which takes place during docking, cell lysis ensues, thereby destroying the living being. Since the chemical structure of the adducts obtained is stable, the contact biocidal long-term effect can be ensured.
    Dioxirane compounds are particularly suitable as polyoxirane compounds for the reaction according to the invention with a 2,2,6,6-tetramethylpiperidine derivative, because a chain structure of the molecules which facilitates the docking of the protozoa is preferred. Di-oxirane compounds that can be beneficially employed for this purpose include bisphenol A diglycidyl ethers and oligomers thereof, glycol / polyglycol diglycidyl ethers, siloxane diglycidyl ethers, polysiloxane dipeoxides, copolymers of ethylene, propylene, styrene with glycidyl monomers, e.g. For example, vinyl glycidyl ether with a proportion of Glycidylcomonomeren from 1 to 50% in the copolymer, and polymers of Methacrylsäureglycidylester.
    The reaction of the 2,2,6,6-tetramethylpiperidine derivative bodies with the dioxirane compounds can be carried out as a standard reaction to then incorporate the resulting antimicrobial agent into the polymer which is to be bio-cidated. However, an in situ reaction directly in the polymer is preferred, with polyaddition taking place without release of waste products to be removed. In this case, the polymer granules, a 2,2,6,6-tetramethyl-piperidine derivative and a poly-oxirane compound according to the invention in a suitable amount, for example, 0.5 to 5 wt.%, Mixed, so that the addition reaction in the extruder, in Injection molding machine, calender and the like. During the necessary for the formation of a workpiece plasticization of the mixture takes place. In this case, the recipe can be adapted to specific requirements at short notice because the reactants are readily available, storable and readily dosed. However, it is also possible to carry out the in situ synthesis with a high concentration of the starting materials, for example 20 to 50% by weight, whereby the 2,2,6,6-tetramethylpiperidine derivative and the dioxirane compound are kneaded in a polymer matrix and the resulting product is granulated to be blended with the polymer to be biocidized.
    As 2,2,6,6-Tetramethylpiperidinderivat can advantageously a compound of the formula η nw ru gi
    0 G CK CH. Where n is a number from 1 to 4, G and G1 independently of one another are hydrogen or methyl and G2 for n = 1 hydrogen is a C1-C18 alkyl which is optionally interrupted by one or more oxygen atoms, cyanoethyl, benzyl, glycidyl, a monovalent radical of an aliphatic, cycloaliphatic, araliphatic, unsaturated or aromatic carboxylic acid, carbamic acid or a phosphorus-containing acid or a monovalent silyl radical, for n = 2, a C2-C12 alkylene, C4-C12 alkenylene, xylylene, a bivalent radical an aliphatic, cycloaliphatic, araliphatic or aromatic dicarboxylic acid, dicarbamic acid or a phosphorus-containing acid or a divalent silyl radical, for n = 3 a trivalent radical of an aliphatic, cycloaliphatic or aromatic tricarboxylic acid, an aromatic tricarbamic acid or a phosphorus-containing acid or a trivalent silyl radical and for n = 4 a vi meaningful radical of an aliphatic, cycloaliphatic or aromatic tetracarboxylic acid.
    As the silyl radical, G 2 is preferably a radical of an aliphatic carboxylic acid having 2 to 18 C atoms, a cycloaliphatic carboxylic acid having 7 to 15 C atoms, an α, β-unsaturated carboxylic acid having 3 to 5 C atoms or an aromatic radical.
    Carboxylic acid used with 7 to 15 carbon atoms, wherein the carboxylic acid may be substituted in each case in the aliphatic, cycloatiphatic or aromatic moiety with 1 to 3 further groups.
    If a monovalent silyl radical is used as G2, the result is, for example, a radical of the formula (CjH 2j) -Si (Z ') 2Z ", where j is an integer between 2 and 5 and Z' and Z" independently of one another are C 1 to C 4 Alkyl or Ci to C4 alkoxy.
    If G2 is a divalent radical of a dicarboxylic acid, the result is, for example, melanic acid, succinic acid, glutaric acid, adipic acid, suberic acid, sebacic acid, maleic acid, itaconic acid, phthalic acid, dibothylmalonic acid, dibenzylmalonic acid, Butyl- (3,5) di-tert-butyl-1-hydroxybenzyl) -malonic acid or bicycloheptene dicarboxylic acid ester.
    If a bivalent radical of a dicarbamic acid is used as G 2, then G 2 can form the corresponding radical of a hexamethylenedicarbamic acid or of 2,4-toluenedicarbamic acid.
    If G2 is a trivalent radical of a tricarboxylic acid, the result is, for example, a trimellitic acid, citric acid or nitrilotriacetic acid radical.
    For a tetravalent radical of a tetracarboxylic acid, for example, G2 may be the tetravalent radical of butane-1,2,3,4-tetracarboxylic acid or of pyromellitic acid.
    Particular preference is given to compounds in which n = 2 and for G1 2 the diacyl radical of an aliphatic dicarboxylic acid having 4 to 12 C atoms is used. Examples of polyakylpiperidine compounds of this type are: 1 4-hydroxy-2,2,6,6-tetramethylpiperidine 2 4-stearoyloxy-2,2,6,6-tetramethylpiperidine 3) 4'methacryloyloxy-1,2,2,6,6 pentamethylpiperidine 4) di (2,2,6,6-tetramethylpiperidin-4-yl) succinate 5) di (2,2,6,6-tetramethylpiperidin-4-yl) gfutarate 6) di {2,2,6, 6-tetramethylpiperidin-4-yl) adipate 7) Di {2,2,6,6-tetramethylpiperidin-4-yl) sebacate 8) Trimellitic acid tri (2,2,6,6-tetramethylpiperidin-4-yl) ester 9) diethylmelonic acid di (2,2,6,6-tetramethylpiperidin-4-yl) ester 10) di (1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin'4-yl) sebacate 11) hexane 1 ', 6'-bis (4-carbamayloxy-1-n-butyl-2,216,6, -tetramethylpiperidine) 12) dimethylbis (2,216,6-tetramethylpipedin-4-oxy) silane 13) phenyltris (2, 2,6) 6-tetramethylpiperidine-4-oxy) silane 14) 4-hydroxy-N-hydroxyethyl-2,2,6,6-tetramethylpiperidine 15) 4-hydroxy-N-2-hydroxypropyl) -2,2,6 , 6-tetramethylpiperidine 16) 1-glycidyl-4-hydroxy-2,2,6,6-tetramethylpiperidine
    A further possibility to use 2,2,6,6-tetramethylpiperidine derivatives advantageously consists in using as 2,2,6,6-tetramethylpiperidine derivative a compound of the formula
    G3 is CH, CH n, where n is 1 or 2, G3 is a diamine, for example an alkylenediamine or phenylenedimine, and G4 is an acololyl radical, for example acetylloxy or benzoyi.
    Examples of polyalkylpiperidine compounds of this type are: 17) N, Ν'-bis (2,2,6,6-tetramethylpiperidin-4-yl) hexamethylene-1,6-diamine 18) N, N'-bis (2 , 2,6) 6-tetramethylpiperidin-4-yl) -hexamethylene-1,6-diacetamide 19) Bis- (2,2,6,6-tetramethylpiperidin-4-yl) -amine * * * ft I lt | ·· I l · · «· t I *» *
    20) 4-benzoylamino-2,2,1,6,6-tetramethylpiperidine 21) N, N '* * * * * t' ll · Φ * * * * · t »i · · -7- -Bis (2,2,6,6-tetramethyl-piperidin-4-yl) N, N'-dibutyl-acipariide 22) N, N'-bis- (2,2,6,6-tetramethyl-piperidin-4 "yl) N 1 N ' -dicyclohexyl-2-hydroxypropylene-1,3-diamine) 23) N, N'-bis {2,2,6,6-tetramethylpiperidin-4-yl) p-xylylenediamine 24) N1N'-bis ( 2,2,6,6-tetramethylpiperidin-4-yl) succindiamide 25) N- (2,2,6,6-tetramethylpiperidin-4-yl) -β-aminodipropionic acid di (2,2,6,6- tetramethyl-piperidin-4-yl) ester or compounds of the formula: 26)
    H3C ch3 Η-N
    h3c ch3
    .NH-C = O C -N-CH 2 CH (OH) CH 2 -o
    27) 28) -8-29) 30) 31)
    y-HN- (2HO) -N- (SHO) -N- (zHO) -HN-Sd
    I I (se
    (W;
    (εε · · * · • • • • • I I I I I I
    36) - 10- C0H 8 '17 ceHlTN' n h3c h3c
    N i H
    CH CH3 3 h3c, ch3
    N-H h3c ch3 2 * 3 37)
    CH3 CH, -CH2-CH (OH) -CH2 h3c h3c
    N i H ch3 CH, 38) 39) -11 - 40) 41)
    42) - 12- R R i 2 '7 m
    43) Further examples of polymeric compounds are reaction products of compounds of the formula
    Epichlorohydrin for polyesters of butane-1,2,3,4-tetracarboxylic acid with a bifunctional alcohol of the formula
    HO CH, l 3 / 'CH, C-CH 2i CH, o- " 7 * Ha ^ -OH C CH-C-CH, / / 1 -ciCw-o' CH3 of the tetracarboxylic acid originating carboxyl side chains are esterified with 2,2,6,6-tetramethyl-4-hydroxypiperidine. 44) CH, i 3 CHf-CH2-CH 0 = C 0 = C i och3
    OR -Jm wherein R represents the 2,2,6,6-tetramethylpiperidine ring. 45)
    - 13-, ch3 H3Cv, CH3 o CH - N N -H2 Η-N N-CH2 H, CCH, h3c ch3 46)> iC F% 0 CH,
    H-N) - O- (CH2) 3-Si-OC ^ H 2 '5 h3c ch3 oc2h5 47)
    48)
    49)
    m = 2-10 50) - 14-
    m = 2-10 51)
    53). "
    - 15 -
    54)
    ο II -C-CH ^ -CH- CO-CH-CH; co 0 II -c-CH, i 3 -O-CH, -C-CH 2 i CH, / Λ O- -ch9 h3c-o 2/2 c / / -ch2 h2c-o
    ch, I 3 CH-C-CH, -o I 2 CHL
    ch3 CH, m 55)
    CH, I 3 -O-CH, -C-CH 2 I CH, o- / -CH 2 / H 2 C-0 ^ CH, I 3 C CH- -c-1 / CH 3 0 -CH 2 h 2c-o m
    ··· * · * «* ·« »* * *« «i · * · ·« «· - 16- 56) 9H3 --Si-o- I {CH2) 3 0
    Examples
    Example 1 45 g (0.1 mol) of N, N'-bisformyl-N, N'-bis (2,2,6,6-tetramethyl-4-piperidinyl) hexamethylenediamine are dissolved in 500 ml of methyl ethyl ketone and with 22.6 g (0.1 mol) of cyclohexane-1,4-dioldigiycidylether and stirred at room temperature for 24 h. The reaction mixture is continuously viscous with slight yellowing. After the reaction time, the highly viscous mass is added with vigorous stirring in 500 ml of methanol and the precipitated adduct 1 finely divided After cooling to about 0 ° C, the pale yellow end product is filtered off, washed with methanol and washed at max. Dried 50 ° C.
    Yield: 60.5 g (89% by weight of the theoretical value)
    Melting point: not detectable, softening from 85 ° C
    In a sample no oxirane structures (H1 nmr / FTIR) can be detected. It can thus be distinguished from a structure of the adduct 1
    starting from x £ 16, target molecular weights in excess of 10,000 daltons are achieved. By kneading 1.5 g of the adduct I with 135 g of HDPE (density 0.951 g / cm3), sample 1 is obtained for biocidal test.
    Example 2
    Analogously to Example 1, 250 g (0.1 mol) of poly [6- (1,1,3,3-tetramethylbutyl) amino-1,3,5-triazine-2,4-diyl (2,2,6,6 -tetramethyl-4-piperidinyl) imino] hexamethylene (2,216,6-tetramethyl [-4-piperidyl] imine with 35 g (0.1 mol) of bisphenol A diglycidyl ether in 1 500 ml of tetrahydrofuran and precipitated by means of 5 000 ml of H 2 O. , isolated and dried.
    Yield: 322 g of adduct 2 1% by weight of adduct 2 are kneaded in PP-R at a density of 0.89 g / cm 3 at 145 ° C. to sample 2.
    Example 3 15 kg of PP-R polypropylene (density 0.89 g / cm 3) are mixed in a single-screw compounder with 160 g (-0.1 mol) of poly [(6-morpholino-s-triazine-2,4-diyl) (2,2,6,6-tetramethyl-4-piperidinyl) imino] hexamethylene (21216,6-tetramethyl-4-piperidinyl) imine and 140 g (0.05 mol) of polydimethylsiloxane having 2 entstehende Glyzidylgruppen of molecular weight 2750 at 200 ° C homogeneously kneaded and then granulated in cold water. The pellets are dried at 30 ° C and form a storage-stable, slightly yellowish opaque polymer composition containing about 2 wt.% Of the adduct 3. From this granulate, injection molding test plates of the format 6 x 6 cm are injected and used for the biocide test as sample 3.
    Example 4 480 g (1 mol) of bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, 1,750 g (1 mol) of difunctionalized polysiloxane according to Example 3 and 12,000 g of polypropylene PP-B (density 0.89 g / cm 3, MFR: 10) are homogeneously kneaded in a single-screw compounder at 180 ° C. and then granulated. The yellowish-colored, opaque granules -18- contains - 20% by weight of the adduct 4. A mixture of 90% by weight PP.R. (density 0.89 g / cm.sup.3, MFR: 0.23) is mixed with 10% by weight. of the adduct 4 extruded into tubes of 25 x 3.4 mm, tube sections are used as sample 4 for the biocide test.
    Example 5 280 g (0.1 mol) of a polypropyl-3-oxy-4- (2,2,6,6-tetramethylpiperidyl) methylsiloxane having a molecular weight of about 2,800 and 275 g (0.1 mol) of a difunctionalized polysiloxane according to Example 3 are incorporated in a total of 30 kg of polyethylene (HDPE, density 0.9 g / cm 3), MFR: 0.55) in the course of film extrusion (220 ° C) and the produced packaging film in a thickness of 25 pm and an adduct content of 1.8% as a sample 5 subjected to a Biocidtest.
    Example 6 156 g (1 mol) of 4-amino-2,2,6,6-tetramethylpiperidine and 500 g (1 mol) of di-alicyclic epoxidized polydimethylsiloxane are distributed on 50 kg of polypropylene granules in a drum mixer and the free-flowing granules of a Tube extrusion fed at 220 ° C. The tubes receive 1.3% by weight of the adduct 6 and are fed as sample 6 to a biocide test.
    Example 7 25 kg of LDPE (density 0.919 g / cm 3) are mixed with 120 g of glycidyl methacylate copolymer having an epoxy equivalent weight of 280 and a molecular weight of 6,800 and 110 g of 1,6-hexanediamine-N, N'-bis (2,2, 6,6-tetramethyl-4-piperidinyl) polymer with 2,6-trichloro-1,3,5-triazine and subsequent reaction with N-butyl-1-butaneamine and N-butyl-2,2,6,6-tetramethyl Homogenized -4-piperidinamine in a drum mixer and then extruded in a single-screw extruder to flexible tubing of dimension 16 x 1 mm. These tubes contain 0.9% by weight of the adduct 7 and are subjected as sample 7 to the biocide test.
    The microbicidal test was performed according to JIS Z 2801: 2000 with Eschericia coli DSM 787 and Staphylococcus aneus DSM 346. The value R of the antimicrobial activity was determined for Gram-positive and Gram-negative bacteria. - 19-
    Fungal growth was tested according to ISO 846, both by Method A, which is suitable for evaluating the resistance of the sample to fungal infestation, if no other usable organic materials are present, and by Method B, which detects the situation of surface contamination of the fungi Sample in practice reflects.
    The test results are summarized in the table below and compared with an untreated sample 8. In column 1, the numbers of the respective sample, in column 2 the weight proportion of the respective adduct in wt.%, In column 3, the polymer type, in columns 4 and 5, the value R of the antimicrobial activity for grampositive (grampos) and gram-negative (gram-neg.) bacteria, in column 6 the A and B values for fungal infestation indicated.
    Sample No. Add u kt polymer R-value fungal attack grampos. Gram-negative. 1 1.1 HDPE 3.6 3.6 ΑΑ00 B01 2 1.0 PP-R> 4.0> 4.0 AAOO B01 3 2.0 PP-R 3.7 4.6 AA01 B11 4 2, 0 PP-B 3.8 4.0 AA01 B01 5 1.8 HDPE 3.8 3.8 AA01 B01 6 1.3 PPH 4.0> 4.10000 B00 7 0.9 LDPE 3.2 3, 0 AA03 B04 8 - PP-R 1.0 1.0 A23 B34 ± i1
    权利要求:
    Claims (5)
    [1]
    Patent Attorneys Dipl.-Ing. Helmut Hübscher Dipl.-Ing. Karl Winfried Hellmich Spittelwiese 7, A 4020 Linz (37 498) II 1. Antimicrobial agent for polymers based on a 2,2,6,6-tetramethyl-piperidine derivative, characterized in that at least two primary or secondary amino groups comprising 2,2,6,6-tetramethylpiperidine derivative of the formula

    I- H3C. CH, H-N V L H3C CH, with n £ 2 by means of a poly-oxirane compound of the formula CHj-CH-R1-CH-CH2 o o converted to a polymeric compound which is the structural unit

    contains at regular intervals.
    [2]
    2. Antimicrobial agent according to claim 1, characterized in that a di-oxirane compound is used as poly-oxirane.
    [3]
    3. Antimicrobial agent according to claim 2, characterized in that the di-oxirane compound is a compound from the group of bisphenol A diglycidyl ethers and oligomers thereof, glycol / polyglycol diglycidyl ether, siloxane diglycidyl ether, polysiloxane dipeoxides, copolymers of ethylene, propylene, styrene with glycidyl mono- meren, z. B. Vinylglycidylether with a proportion of Glycidylcomonomeren from 1 to 50% in the copolymer, and polymers of Methacrylsäureglycidylester is used,
    [4]
    4. A method for equipping a polymer with an antimicrobial agent according to any one of claims 1 to 3, characterized in that a polymer granules, the 2,2,6,6-Tetramethylpiperidinderivat with the at least two primary or secondary amino groups and the poly-oxirane compound are admixed and that the mixture is plasticized in a conventional manner and formed into a workpiece,
    5. The method according to claim 4, characterized in that based on the total weight of the mixture 0.5 to 5.0 wt.% Of 2,2,6,6-tetramethylpiperidine derivative and poly-oxirane compound are admixed with the polymer granules Linz, am September 28, 2010 KE-KELIT Kunststoffwerk Gesellschaft mbH

    by: Patent Attorneys Dipl.-Ing. Helmut Hübscher Dipl.-Ing. Karl Winfried Hellmich Spittelwiese 7, A 4020 Linz A 1622/2010, A01N New claims (37 498) II Claims 1. Use of a 2,2,6,6-tetramethylpiperidine derivative of the formula comprising at least two primary or secondary amino groups

    with n £ 2 as an antimicrobial agent for polymers, wherein the 2,2,6,6-tetramethylpiperidine derivative is reacted by means of a Polyoxiranverbindung the formula CH - CH-R1-CH-CH2 O 0 to a polymeric compound which is the structural unit

    contains at regular intervals. REPLACED | 2 2, use according to claim 1, characterized in that as Po-lyoxiranverbindung a Dioxiranverbindung is used. 3, use according to claim 2, characterized in that the dioxirane compound is a compound from the group of bisphenol A diglycidyl ethers and oligomers thereof, Giycol / polyglycol diglycidyl ether, Siloxandiglycidylether, polysiloxanipoxides, copolymers of ethylene, propylene, styrene with glycidyl monomers, preferably Vinyl glycidyl ether with a proportion of glycidyl comonomers of 1 to 50% in the copolymer, and polymers of glycidyl methacrylate is used. 4, use of an antimicrobial agent according to any one of claims 1 to 3 for equipping a polymer, characterized in that the polymer granules 2,2,6,6-Tetramethylpiperidinderivat with the at least two primary or secondary amino groups and the Polyoxiranverbindung are admixed and that the Mixtured plasticized in a conventional manner and formed into a workpiece.
    [5]
    5. Use according to claim 4, characterized in that, based on the total weight of the mixture 0.5 to 5.0 wt.% Of 2,2,6,6-tetramethylpiperi-dine derivative and Polyoxiranverbindung the polymer granules are admixed. Linz, January 10, 2012 KE-KELIT Kunststoffwerk Gesellschaft m.b.H. By J

    submitted
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    同族专利:
    公开号 | 公开日
    EP2436266A1|2012-04-04|
    AT510488B1|2012-09-15|
    EP2436266B1|2018-04-04|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    JPS6332782B2|1977-08-08|1988-07-01|Sankyo Kk|
    EP0003542B1|1978-02-08|1981-11-25|Ciba-Geigy Ag|Polyalkylpiperidine derivatives of s-triazines, their use as stabilizers for polymers and polymers thus stabilized|
    US4348524A|1980-03-28|1982-09-07|Ciba-Geigy Corporation|Amide derivatives of polyalkylpiperidines|
    DE3901246A1|1989-01-18|1990-07-19|Basf Ag|USE OF 2,2,6,6-TETRAMETHYL-4-AMINOPIPERIDINAMIDES AS A FUNGICIDE|
    US6200583B1|1998-03-24|2001-03-13|Dainichiseika Color & Chemicals Mfg. Co., Ltd.|Antimicrobial agents, antimicrobial resin compositions, and articles having antimicrobial activity|EP2989154A1|2013-04-22|2016-03-02|Jansen AG|Plastic having a biocidal surface and method for producing said plastic|
    EP2824139A1|2013-07-12|2015-01-14|Jansen AG|Plastic with a biocidal surface and method of making same|
    法律状态:
    2020-08-15| MM01| Lapse because of not paying annual fees|Effective date: 20190929 |
    优先权:
    申请号 | 申请日 | 专利标题
    ATA1622/2010A|AT510488B1|2010-09-29|2010-09-29|ANTIMICROBIAL MEANS FOR POLYMERS|ATA1622/2010A| AT510488B1|2010-09-29|2010-09-29|ANTIMICROBIAL MEANS FOR POLYMERS|
    EP11183036.0A| EP2436266B1|2010-09-29|2011-09-28|Antimicrobial agent for polymers|
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