EP3078733B1 - Spülen von polycarbonat - Google Patents

Spülen von polycarbonat Download PDF

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Publication number
EP3078733B1
EP3078733B1 EP16168259.6A EP16168259A EP3078733B1 EP 3078733 B1 EP3078733 B1 EP 3078733B1 EP 16168259 A EP16168259 A EP 16168259A EP 3078733 B1 EP3078733 B1 EP 3078733B1
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EP
European Patent Office
Prior art keywords
polycarbonate
composition
rinsing
rinse aid
cleaning
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.)
Not-in-force
Application number
EP16168259.6A
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English (en)
French (fr)
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EP3078733A1 (de
Inventor
Thomas Tyborski
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ecolab Inc
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Ecolab Inc
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Priority to EP16168259.6A priority Critical patent/EP3078733B1/de
Publication of EP3078733A1 publication Critical patent/EP3078733A1/de
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Publication of EP3078733B1 publication Critical patent/EP3078733B1/de
Not-in-force legal-status Critical Current
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10—Objects to be cleaned
    • C11D2111/14—Hard surfaces
    • C11D2111/18—Glass; Plastics

Definitions

  • the present invention relates to rinsing compositions for the purpose of rinsing surfaces, preferably wherein the surfaces comprises at least partially polycarbonate surfaces.
  • the present invention also relates to corresponding methods of rinsing surfaces.
  • polymeric materials are frequently used.
  • PET polyethylene terephthalate
  • polyarcylate polycarbonate and the like may be present in molds, for example chocolate molds, in bottles such as soda bottles, in food and beverage plant equipment, and the like.
  • polycarbonate is used for bottle material and dairy industries (water, milk, baby bottles).
  • Polycarbonate is also used in institutional markets for trays but also for roofs, e.g. railway stations, stadiums, arenas.
  • polycarbonate is used for dialysis, connectors and appliance systems.
  • polycarbonate is used for machinery parts such as cover of e.g. slicers, packaging machines and for separation between different production areas.
  • alkaline composition e.g. based on sodium/potassium hydroxide.
  • This caustic/alkaline detergents may contain surfactants.
  • oxidizers e.g. chlorine, are added to alkaline cleaning formulations. These products are used in a concentration from 0.3 to 20 %.
  • the cleaning of bottles, trays and molds in normal cases takes place in a tunnel washing machine by spraying the detergent on the polycarbonate surfaces.
  • stress cracking is highly undesirable for several reasons. In the case of molds stress cracking can cause problems when the mold leaves polycarbonate fragments in the product. In some cases stress cracking can cause processing lines to shut down which is very costly for a plant.
  • US patent 3,993,575 discloses an acid cleaner and brightener concentrate composition comprising a dicarboxycic acid, an amine and water having an pH of about 1 to about 3 which is useful in the removal of tenacious soil from vehicles without subsequent harm to surfaces including coated polycarbonate glass substitute.
  • US 4,505,836 discloses a process of cleaning a polycarbonate surface or bottle including washing the surface or bottle with a composition consisting essentially of an aqueous basic solution containing the members: alkali metal carbonate, alkali metal bi-carbonate an a mixture of mono- and diesters of phophoric acid and then rinsing the surface or bottle with water.
  • US 5,223,162 discloses a washing composition for inhibiting stress cracking in poly(alkaline terephthalate) or polycarbonate articles by applying to the article a hydrophilic substituted aromatic hydrocarbon having either an alkyl or aryl side chain such as a sodium sulfonate.
  • the washing composition is prepared from a concentrate comprising an alkaline metal hydroxide, a chelant or sequestrant, the stress cracking inhibitor and water.
  • WO97/06229 it is disclosed that many conventional aqueous alkaline and acid cleaners promote stress cracking of polycarbonate plastics. Said WO97/06229 therefore provides an aqueous liquid composition containing dihydrogenphosphate salt, sulfur containing surfactant and preferably a small amount of phosphoric acid which is stated to clean soiled metal surfaces without damaging plastic parts, especially made of polycarbonate, that come into contact with the composition.
  • EP0844301 discloses that mold removal from plastic bottles such as polyesterant polycarbonate bottles can be significantly enhanced by adding to a typical caustic soaking solution an effective amount of a complex polyphosphate such as sodium tri-poly phosphate and a surfactant. It is further disclosed that mold removal can be further enhanced by combining with the phosphate and surfactant either a phosphonate and/or a chelating agent such as sodium glucoheptonate. This combination is stated to significantly improve mold removal but does not increase stress cracking of the plastic bottle.
  • WO98/59072 discloses an additive for a detergent formulation comprising a sequestrant preferably selected from the group of nitrilo tracetic acid (NTA), beta-alanine diacetic acid ( ⁇ -ADA), methyl glycine diacetic acid (MGDA), serin diacetic acid (SDA) and ethyl glycine diacetic acid (EGDA) and further comprising a non-ionic surfactant and or a hydrotrope.
  • NTA nitrilo tracetic acid
  • ⁇ -ADA beta-alanine diacetic acid
  • MGDA methyl glycine diacetic acid
  • SDA serin diacetic acid
  • EGDA ethyl glycine diacetic acid
  • DE10 2004 055 492 discloses a rinsing composition for automatic dishwashing, especially suitable for rinsing plastic articles.
  • Said rinsing composition comprises C 8 -C 20 -alkyl-bis-(2-hydroxy alkyl) amine as a detergent compound as well as at least one acid compound.
  • the rinsing composition is stated to reduce or to inhibit the occurrence of stress cracking in the plastic article.
  • WO 01/42411 discloses compositions including ether-capped poly(oxyalkylated) alcohol surfactants having superior grease cleaning abilities and improved spotting/filming benefits.
  • good soil carrying and anti organic depositing e.g. cacao pigments
  • anti scaling e. g. mineral deposits from hard water
  • an aqueous rinse aid composition for rinsing surfaces preferably wherein the surfaces comprises at least partially polycarbonate surfaces, comprising:
  • the invention refers to:
  • the cleaning composition described herein does not comprise NaOH, KOH, other hydroxides, nitrilotriacetic acid (NTA) or ethylene diamino tetraacetic acid (EDTA) or combinations thereof.
  • NTA nitrilotriacetic acid
  • EDTA ethylene diamino tetraacetic acid
  • the cleaning composition described herein is highly compatible with polycarbonate materials and do not cause any stress cracking but is very suitable to remove deposits, especially chocolate deposits. This will be shown in detail in the examples below.
  • the one or more surfactants are non-ionic and/or anionic surfactants. From the group of the non-ionic surfactants there are preferred especially the branched ethoxylated and or propoxylated C 10 -C 22 alcohols having a degree of ethoxylation and/or propoxylation of 1 to 10, preferably a C 16 guerbet alcohol having a degree of ethoxylation of 2.
  • non-ionic surfactants are alkylpolyglycosides; amineoxides, e.g. laurylamine; copolymeric carboxylates, e.g. acrylic/maleic copolymers or other copolymers of either maleic or acrylic acid; and hydrotropes, e.g. octyliminodipropionate.
  • these surfactants are less suitable for so-called cleaning-in-the-place (CIP) or passing-through applications as long as no antifoaming agents are added or the concentration of said amines is not very low.
  • Suitable surfactants are the surfactants nrs. 1, 2, 24, 46, 51 (alkylpolyglycosides), nrs. 19, 50, 53, 59 (anionic surfactants), nr. 47 (amineoxide), nr. 3 (amphoteric surfactant), nrs. 23, 38, 39, 57 (non-ionic surfactants) and nrs. 48, 49 disclosed below in table 4.
  • anionic surfactants phosphate polyether ester and/or alkylated aryl sulphonates, especially the alkali cumene sulphonates, are preferred. These surfactants do not only improve the cleaning properties of the cleaning composition described herein and have the function to facilitate the drying process due to their ability to reduce interfacial tension but furthermore have good material compatibility properties.
  • the di- or oligoimides derived from dicarbocylic acids used as chelating agent in the cleaning composition described herein are di- or oligoimides derived from C 2 - C 6 alkyl diacids, preferably derived from succinic acids, and most preferably an iminodisuccincic acid salt, e.g. the sodium salt ( CAS-No. 144538-83-0 ). These di- or oligoimides are preferably present in the aqueous cleaning composition in an amount of 10 to 90 weight %, preferably in an amount of 20 to 60 weight %.
  • the sequestring agents are present in the cleaning composition described herein in order to inhibit crystal growth which would lead to limestone deposits.
  • the sequestring agents are selected from the group of polyphosphates, gluconic acid, polycarboxylic acids, hydroxy polycarboxylic acids, phosphonic acids, and the water-soluble salts thereof.
  • Examples of appropriate sequestring agents are penta sodium triphosphate, citric acid, 2-phosphonobutane-1,2,4-tricarboxylic acid, and the water-soluble salts thereof. Even if not preferred also nitrilotriacetic acid (NTA) and/or ethylene diamino tetraacetic acid (EDTA) may be used as sequestring agents.
  • NTA nitrilotriacetic acid
  • EDTA ethylene diamino tetraacetic acid
  • NTA and EDTA are not preferred due to their alkalinity, their toxicity and harmfulness to the environmental.
  • sequestring agents are methyl glycin diacetic acid, dicarboxymethyl-L-glutamic acid, serine diacetic acid, imidosuccinic acid, poly acrylic acids and copolymers of maleic anhydride and acrylic acids as well as salts thereof.
  • Commercially available are e.g. Sokalan® CP5 and PA 30 from BASF, Alcosperse® 175 and 177 from Alco, LMW ® 45 N and SPO2 ND from Norsohaas.
  • Suitable natural polymers are for example oxidized starch (e.g.
  • suitable phosphonic acid are e.g. 1-hydroxyethyl-1,1-diphosphonic acid, diethylen triamine pentamethylen phosphonic acid or ethylen diamin tetramethylen phosphonic acid or salts thereof.
  • the sequestring agent is preferably present in an amount of 1 to 30 weight %, preferably in an amount of 5 to 20 weight %.
  • a particularly preferred sequestring agent is a mixture of a tripolyphosphate and a gluconate, for example potassium tripolyphosphate and sodium gluconate. If a mixture of tripolyphosphate and sodium gluconate is used the polyphosphate is present in an amount of 0.5 to 10 weight %, preferably 1 to 4 weight %, and the gluconate is present in an amount of 1 to 20 weight %, preferably 3 to 10 weight %.
  • the cleaning composition described herein is free of NaOH, KOH, other hydroxides, nitrilotriacetic acid (NTA) or ethylene diamino tetraacetic acid (EDTA) or combinations thereof in order not to damage said surfaces.
  • NTA nitrilotriacetic acid
  • EDTA ethylene diamino tetraacetic acid
  • the cleaning composition described herein may further comprise a stabilizing agent, preferably selected from the group comprising propylene glycol butylether, ethanol, isopropylether, n-propanol, and other glycoles.
  • the stabilizing agent is preferably present in an amount of 0.1 to 10 weight %, preferably in an amount of 0.5 to 5 weight %.
  • the pH value of the cleaning composition described herein should be below 11 and preferably below 10.5. However, in order to provide good cleaning properties it is preferred that the pH value is not below 7, preferably not below 8 since the sequestring agents have only a poor or even no performance in neutral or acidic range.
  • the aqueous cleaning composition comprises a) the water in an amount of 10-90 wt.-%, b) the di- or oligoimide derived from dicarboxylic acids or salt thereof in an amount of 10-90 wt.-%, c) the sequestring agent(s) in an amount of 0.5-10 wt.-%, and d) the surfactant(s) in an amount of 1-20 wt.-%.
  • the aqueous cleaning composition comprises: a) water in an amount of 10-90 wt.-%, and b) an iminooligosuccinate in an amount of 10-90 wt.-%, and c) tripolyphosphat in an amount of 0.5-10 wt.-%, and/or d) a gluconate in an amount of 1-20 wt.-%, and e) a phosphate polyether ester in an amount of 0.05-5 wt.-%, and f) propylene glycol butylether in an amount of 0.1-10 wt.-%.
  • the above cleaning composition can be prepared from a concentrate composition containing less or even no water in order to save weight and volume which might be desirable for storing and/or transportation purposes.
  • the components of the concentrate composition are the same as for the aqueous cleaning composition except for water which is added to said concentrate composition prior to the use of the resulting aqueous cleaning composition.
  • aqueous cleaning composition and concentrate composition may be used for the purpose of cleaning surfaces, preferably wherein the surfaces comprise at least partially a polycarbonate surface.
  • plastic surfaces as for example polyacrylate, polyethylene, polyoxymethylene (POM), can also be cleaned with the compositions described herein without the risk of damages due to for example stress cracking.
  • plastic surfaces not sensitive to stress cracking e.g. thermoplastic polymers and elastomers, can be cleaned with the compositions described herein.
  • an aqueous rinse aid composition for rinsing surfaces preferably wherein the surfaces comprises at least partially polycarbonate surfaces, comprising:
  • the rinse aid composition of the present invention is highly compatible with polycarbonate materials and does not cause any stress cracking, but is very suitable to remove deposits, especially chocolate deposits. This will also be shown in detail in the examples below.
  • the aqueous rinse aid composition further comprises a stabilizing agent as for example propyleneglycolbutylether, ethanol, isopropylether, n-propanol, and other glycoles, preferably propyleneglycolbutylether.
  • a stabilizing agent as for example propyleneglycolbutylether, ethanol, isopropylether, n-propanol, and other glycoles, preferably propyleneglycolbutylether.
  • the above-mentioned C16 guerbet alcohol having a degree of ethoxylation of 2 is present in an amount of 1 to 15 wt.-%, preferably in an amount of 3 to 8 wt.-%.
  • the cumene sulphonate is present in an amount of 5 to 50 wt.-%, preferably in an amount of 15 to 35 wt.-%.
  • the above stabilizing agent preferably propyleneglycolbutylether, may be present in an amount of 1 to 30 wt.-%, preferably in an amount of 5 to 15 wt.-%.
  • the rinse aid composition of the present invention is preferably free of NaOH, KOH, other hydroxides, nitrilotriacetic acid (NTA) or ethylene diamino tetraacetic acid (EDTA) or combinations thereof in order not to damage the surfaces to be rinsed, especially polycarbonated surfaces, especially in the cases where the applied rinse aid composition is not removed from said surfaces after its application.
  • NTA nitrilotriacetic acid
  • EDTA ethylene diamino tetraacetic acid
  • the above aqueous rinse aid composition may be prepared from a concentrate composition containing less or even no water in order to save weight and volume which may be desirable for storing or transportation purposes.
  • the components of the concentrate composition are the same as for the aqueous rinse aid composition except for water which is added to said concentrate composition prior to the use of the resulting aqueous rinse aid composition.
  • the aqueous rinse aid composition and concentrate composition may be used for the same purposes as mentioned above for the cleaning compositions.
  • the present invention also includes a method of using the rinse aid compositions described herein to rinse polymeric surfaces, especially polycarbonate surfaces.
  • the compositions may be applied to a polymeric surface in several ways including spraying, pouring, wiping, dipping, misting, rolling, and foaming the composition onto the polymeric surface. Further, the composition may be applied manually or as part of a clean-in-place cleaning program.
  • Described herein but not part of the present invention is also a method of cleaning and optionally rinsing a surface, preferably wherein the surface comprises at least partially a polycarbonate surface, comprising the steps: a) applying to the surface the cleaning composition as described above, and b) optionally removing the cleaning composition from the surface, preferably by rinsing the surface with water, and/or c) optionally applying to the surface the rinse aid composition according as described above, and d) optionally removing the rinse aid composition from the surface, preferably by drying with warm or hot air.
  • a method of rinsing a surface preferably wherein the surface comprises at least partially a polycarbonate surface, comprising the steps: a) applying to the surface the rinse aid composition as described above, and b) optionally removing the rinse aid composition from the surface, preferably by drying with warm or hot air.
  • compositions When applied to a polymeric surface, the compositions are preferably applied at temperatures in the range of 20-70°C, preferably 40-60°C.
  • the rinsing compositions according to the present invention have superior properties with respect to rinsing performance, soil carrying ability (dispersing ability), ability to inhibit lime deposition (mineral deposits from hard water), ability to inhibit organic deposition (e.g. cacao pigments), possibility to monitor the concentration of the rinsing composition by conductivity and with respect to material compatibility.
  • Table 1 shows the respective performances of chlorine-alkaline, strong caustic and acidic cleaners as well as of the cleaner compositions described herein.
  • Table 1 Performances of various cleaning compositions Performance of alkaline chlorinated formulations alkaline formulations acidic formulations formulation described herein cleaning +++ +++ - +++ soil carrying o o/++ - ++ scale inhibiting - -/o +++ ++ inhibiting of organic deposits (cacao pigments) o o/+ - ++ online control ⁇ +++ +++ ++ material compatibility (polycarbonate) - - +++ ++/+++ +++: excellent, ++: very good, +: good, o: only in some cases applicable, -: inapplicable
  • Example 1 Table 2 shows the conditions and results of impact tests of traditional cleaner compositions on polycarbonate surfaces.
  • Table 2 shows the conditions and results of impact tests of traditional cleaner compositions on polycarbonate surfaces.
  • A2 Tensile bars showed tensile elongation till just after yield.
  • A3 Tensile bars showed elongation till yield only.
  • A4 Tensile bars showed visible signs of crazing effects.
  • A5 Tensile bars already broken in testing. W: Whitening effects, even after cleaning. C: Crazes visible. D: Surface defects other then crazes.
  • Example 2 Table 3 shows the conditions and results of impact tests of various substances, e.g. whole milk chocolate, NTA, EDTA or pure sodium gluconate, and of the cleaning and rinsing compositions described herein and rinsing composition T according to the present invention on polycarbonate surfaces.
  • a solution of a composition in demineralized water was prepared and applied to a polycarbonate test piece for 168 hours at 50 °C. Thereafter the polycarbonate surface was visually evaluated for defects in the surface. Results are shown in table 3.
  • Table 3 Conditions and results of impact tests of various substances and of the cleaning and rinsing compositions described herein and rinsing composition T according to the invention on polycarbonate surfaces.
  • Example 3 Table 4 shows the conditions and results of impact tests of various surfactants and of the guerbet alcohol Dehydol G162 used in the rinse aid composition of the invention on polycarbonate surfaces.
  • a solution of a surfactant in demineralized water was prepared and applied to a polycarbonate test piece for 168 hours at 50 °C. Thereafter the polycarbonate surface was visually evaluated for defects in the surface. Results are shown in table 4.
  • results in table 4 shows that only a few surfactants pass all tests with the result N (no attacks, no defects).
  • Those surfactants which show good material compatibility i.e. surfactants nr. 1-3, 19, 24, 38, 39, 46-51, 53, 57 und 59, have, however, the disadvantages of being too much foaming (nr. 2, 19, 24, 46, 47, 51, 53, 59 but could possibly combined with a non foaming/defoaming surfactant e. g. 23, 38, 39) and/or having poor surface tension reducing properties (nr. 57).
  • most of the surfactants mentioned in table 4 have both poor material compatibility as well as the additional disadvantages mentioned above.
  • Dehydol G 162 (nr. 23) is the only surfactant having passed all tests with N and additionally having no such disadvantages than other surfactants as mentioned above. Therefore, Dehydol G 162 has superior properties in CIP- and spray applications.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Claims (5)

  1. Wässrige Klarspülerzusammensetzung zum Spülen von Oberflächen, vorzugsweise wobei die Oberflächen mindestens teilweise Polycarbonatoberflächen umfassen, umfassend:
    a) 1-15 Gew.-% eines C16-Guerbet-Alkohols, der einen Ethoxylierungsgrad von 2 aufweist,
    b) 5-50 Gew.-% eines Cumol-Sulfonats,
    c) 20-95 Gew.-% Wasser, und optional
    d) 1-30 Gew.-% eines Stabilisierungsmittels.
  2. Wässrige Klarspülerzusammensetzung nach Anspruch 1, wobei der pH-Wert der wässrigen Klarspülerzusammensetzung im Bereich zwischen 3 und 9 liegt.
  3. Wässrige Klarspülerzusammensetzung nach Anspruch 2, wobei der pH-Wert der wässrigen Klarspülerzusammensetzung im Bereich zwischen 7 und 9 liegt.
  4. Verwendung einer Zusammensetzung nach einem der Ansprüche 1 bis 3 zum Zwecke des Spülens von Oberflächen, vorzugsweise wobei die Oberflächen mindestens teilweise Polycarbonatoberflächen umfassen.
  5. Verfahren zum Spülen einer Oberfläche, vorzugsweise wobei die Oberfläche mindestens teilweise eine Polycarbonatoberfläche umfasst, umfassend die Schritte:
    a) Anwenden der Klarspülerzusammensetzung nach einem der Ansprüche 1 bis 3 auf der Oberfläche, und
    b) optional Entfernen der Klarspülerzusammensetzung von der Oberfläche, vorzugsweise durch Trocknen mit warmer oder heißer Luft.
EP16168259.6A 2007-05-11 2007-05-11 Spülen von polycarbonat Not-in-force EP3078733B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP16168259.6A EP3078733B1 (de) 2007-05-11 2007-05-11 Spülen von polycarbonat

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP16168259.6A EP3078733B1 (de) 2007-05-11 2007-05-11 Spülen von polycarbonat
EP07729011.2A EP2152842B1 (de) 2007-05-11 2007-05-11 Verfahren zum säubern von polycarbonat
PCT/EP2007/054559 WO2008138392A1 (en) 2007-05-11 2007-05-11 Cleaning of polycarbonate

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
EP07729011.2A Division-Into EP2152842B1 (de) 2007-05-11 2007-05-11 Verfahren zum säubern von polycarbonat
EP07729011.2A Division EP2152842B1 (de) 2007-05-11 2007-05-11 Verfahren zum säubern von polycarbonat

Publications (2)

Publication Number Publication Date
EP3078733A1 EP3078733A1 (de) 2016-10-12
EP3078733B1 true EP3078733B1 (de) 2018-09-05

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EP16168259.6A Not-in-force EP3078733B1 (de) 2007-05-11 2007-05-11 Spülen von polycarbonat
EP07729011.2A Not-in-force EP2152842B1 (de) 2007-05-11 2007-05-11 Verfahren zum säubern von polycarbonat

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Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3928602A1 (de) * 1989-08-30 1991-03-07 Henkel Kgaa Alkalistabile und stark alkalisch formulierbare antischaummittel fuer die gewerbliche reinigung, insbesondere fuer die flaschen- und cip-reinigung
ATE221569T1 (de) * 1996-04-16 2002-08-15 Procter & Gamble Ausgewählte mitten in der kette verzweigte oberflächenaktive substanzen enthaltende flüssige reinigungsmittel
US6093856A (en) * 1996-11-26 2000-07-25 The Procter & Gamble Company Polyoxyalkylene surfactants
JP4069968B2 (ja) * 1997-10-14 2008-04-02 ザ プロクター アンド ギャンブル カンパニー 中鎖分枝鎖界面活性剤を包含する軽質液体またはゲル食器洗浄用洗剤組成物
EP1047761A1 (de) * 1997-10-14 2000-11-02 The Procter & Gamble Company Seitenkettige tenside enthaltende spülwaschmittelzusammensetzungen für harte oberflächen
WO1999019450A1 (en) * 1997-10-14 1999-04-22 The Procter & Gamble Company Aqueous and non-aqueous heavy duty liquid detergent compositions comprising mid-chain branched surfactants
DE69924874T2 (de) * 1998-12-10 2005-11-17 Unilever N.V. Verwendung von waschmittelzusammensetzungen
EP1235892A1 (de) * 1999-12-08 2002-09-04 The Procter & Gamble Company Zusammensetzungen enthaltend etherverschlossene polyoxyalkylierte tensidalkohole
US6627591B2 (en) * 1999-12-17 2003-09-30 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Dye fixing composition
DE10100720A1 (de) * 2001-01-10 2002-07-11 Beiersdorf Ag Kosmetische und dermatologische waschaktive Zubereitungen, enthaltend eine wirksame Menge an Iminodibernsteinsäure und/oder ihren Salzen
US6546940B1 (en) * 2001-09-10 2003-04-15 Johnsondiversey, Inc. Cleaning composition and method for using the same
US7056874B2 (en) * 2002-09-23 2006-06-06 Ecolab Inc. Cleaning solutions for carbon removal
GB0522658D0 (en) * 2005-11-07 2005-12-14 Reckitt Benckiser Nv Composition

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Publication number Publication date
EP2152842B1 (de) 2017-10-11
WO2008138392A1 (en) 2008-11-20
EP2152842A1 (de) 2010-02-17
EP3078733A1 (de) 2016-10-12

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