JP5894146B2 - レオロジー改変された低発泡性液体抗菌組成物及びその使用方法 - Google Patents
レオロジー改変された低発泡性液体抗菌組成物及びその使用方法 Download PDFInfo
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- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
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Description
本発明がより容易に理解されるように、一定の用語を最初に定義する。以下の定義される用語については、異なる定義が請求項中又は本明細書中の他所で示されない限り、これらの定義が適用される。
Generally Regarded As Safe(GRAS)に列挙された陰イオン界面活性剤の良好な洗浄力及び広い殺生物効力は、それらを農産物洗浄剤処方の活性成分としての使用に理想的なものとする。しかしながら、これらの界面活性剤の高い発泡性は、それらをEcolabから入手可能なOasis Proアスピレーターディスペンサーなどの自動分配装置に適した便利な液体形態中で使用されるのには困難なものとする。分配装置はしばしば、濃縮形態からの分配過程の間に、大量の安定な泡を生成する。泡の存在は、リンスを含まない農産物洗浄剤処方などのリンスを含まない処方において使用される場合、それは、接触表面の視覚的外観に影響を及ぼすだけでなく、農産物などの接触表面の味、匂い、テクスチャー及び外観も変化させうるために、有害である。
いくつかの側面においては、組成物は抗菌剤を含む。いくつかの実施態様においては、本発明の組成物とともに使用されるのに適した抗菌剤は、GRAS抗菌剤又は食品グレードの組成物である。
組成物はさらに、消泡剤を含む。いくつかの実施態様においては、組成物は、食品グレードの品質の消泡剤を含むことができる。この目的を達成するために、シリコーンが有効な消泡剤として使用可能である。組成物は、組成物が液体形態であるにもかかわらず、消泡剤としてシリコーンが取り込まれることができるように設計される。ジメチルシリコーン、グリコールポリシロキサン、メチルフェノールポリシロキサン、トリアルキル又はテトラアルキルシラン、疎水性シリカ消泡剤及びそれらの混合物などのシリコーンはすべて、組成物中で消泡剤として使用可能である。一般的に入手可能な市販の消泡剤は、有機エマルジョン中に結合されたシリコーンであるArmour Industrial Chemical CompanyからのArdefoam(登録商標);シリコーン及びノンシリコーンタイプの消泡剤並びにシリコーンエステルであるKrusable Chemical Companyから入手可能なFoam Kill(登録商標)又はKresseo(登録商標);及びDow Corning Corporation から商業的に入手可能なAnti-Foam A(登録商標)及びDC-200を含む。本組成物とともに使用されるのに適した他の追加の消泡剤は、Dow Corning Corporation から商業的に入手可能なFG10及び1520並びにLambentから商業的に入手可能なHodag FD-82Kを含むが、これらに限定されない。消泡剤は、約0.01重量%〜20重量%、約0.1重量%〜10重量%、又は約0.01重量%〜約2重量%の濃度範囲で存在することができる。いくつかの実施態様においては、組成物は、ゼロ超であるが1重量%未満の消泡剤を含む。当然のことながら、これらの値及び範囲の間のすべての値及び範囲は、本開示に組み込まれる。
いくつかの実施態様においては、組成物は酸味料を含む。酸味料は、約1以下のpHを有する濃縮組成物を生成するための有効量で存在することができる。他の実施態様においては、酸味料は、約5、約5以下、約4、約4以下、約3、約3以下、約2、約2以下などのpHを有する使用組成物を生成するための有効量で存在することができる。いくつかの実施態様においては、組成物は、約0〜約6、約1〜約5、又は約2〜約4の間のpHを有する。他の実施態様においては、組成物は、約3.2未満のpHを有する。
いくつかの実施態様においては、組成物は、安定化剤も含む。いくつかの実施態様においては、安定化剤は、食品グレード又はGRAS安定化剤である。安定化剤は、組成物の安定性を維持することを助ける。例えば、いくつかの実施態様においては、安定化剤は、硬水中での組成物の安定性を維持することを助ける。いくつかの実施態様においては、安定化剤は、組成物が500ppmの硬水で希釈された場合、少なくとも24時間、沈澱の生成を防ぐための有効量で存在する。
組成物は、増粘剤も含む。増粘剤は、食品グレード又はGRASであることができる。増粘剤は、組成物の粘度を増加させ、そして酸性条件下での組成物中への消泡剤の取り込みを可能とする。すなわち、増粘剤は、消泡剤が存在する場合に、相安定な組成物を維持する有効量で存在する。
いくつかの実施態様においては、組成物はキャリアーを含む。キャリアーは、組成物の他の成分を溶解し、懸濁し、又は担持する媒体を提供する。キャリアーの濃度及びタイプは、全体としての組成物の性質、貯蔵環境、及び他の因子の中でも、抗菌剤の濃度を含む適用方法に依存するだろう。特に、キャリアーは、本発明の組成物中の活性剤の抗菌有効性を阻害しない濃度が選ばれ、そして使用されるべきである。食品接触表面、すなわち、農産物、を洗浄するために使用される場合、選ばれたキャリアーは、食品接触表面に悪影響を及ぼさないものであるべきである。
いくつかの実施態様においては、組成物は、1つ以上の染料を含む。染料は、食品グレード又はGRAS染料であることができる。染料は、抗菌組成物が、シンク中又は洗浄水などの処理溶液中に存在するという証拠を提供することを助ける。組成物とともに使用されるための染料は、約2未満のpHなどの低いpHにおいて安定でなければならない。開示された組成物とともに使用するのに好適な染料は、FD&C Green 3、FD&C Yellow 5及びそれらの混合物を含むが、これらに限定されない。
本発明の組成物は、追加の成分を含むことができる。追加の成分は、界面活性剤、加工助剤、着色剤、着香剤、抗褐変剤、及びそれらの混合物を含むことができるが、これらに限定されない。
組成物は、濃縮組成物と使用組成物を含む。例えば、濃縮組成物は、水などで希釈されて、使用組成物を生成することができる。ある実施態様においては、濃縮組成物は、対象への適用の前に、使用溶液に希釈されることができる。経済的理由から、濃縮物が販売されることができ、そしてエンドユーザーが該濃縮物を水又は水性希釈剤で使用溶液に希釈することができる。他の実施態様においては、使用組成物は、約0.01〜約10重量%の濃縮組成物及び約90〜約99.99重量%の希釈剤;又は約0.1〜約2重量%の濃縮組成物及び約98〜約99.9重量%の希釈剤を含むことができる。
いくつかの側面においては、本開示は、抗菌組成物を適用するのに適した任意の方法又は器械を使用して、該組成物と食品製品を接触させる方法を提供する。食品製品への接触は、田畑、加工場所又は工場、車両、倉庫、店、レストラン又は家庭などの食品製品が見出されるかもしれない任意の場所において行われることができる。これらの同じ方法が、他の対象物への組成物の適用にも適応可能である。
代表的な農産物洗浄剤処方への消泡剤の添加の影響を評価するために、試験を行った。3つの製剤を試験した。組成物A及びBを、本開示の実施態様に従って調製した。組成物A及びBを以下の表に示す。
実施例1で上記した組成物A及びBを用いた試験を、レタス上への残留化学物質のキャリーオーバーを本発明の様々な農産物洗浄剤の泡の高さと濃度の関数として評価するために実施した。
本開示の実施態様による抗菌性の農産物洗浄剤組成物の、フルーツ及び野菜の処理用水中のリステリア・モノサイトゲネス、エシェリキア・コリO157:H7及びサルモネラ・エンテリカを減少させる能力を測定するために試験を行った。農産物洗浄剤の処方も以下の表に示す。
本開示の実施態様による代表的な農産物洗浄剤組成物の、ほうれん草の葉の表面上のリステリア・モノサイトゲネス、エシェリキア・コリO157:H7及びサルモネラ・エンテリカを減少させるための残留有効性を評価するために試験を行った。以下の農産物洗浄剤組成物をこの試験のために使用した。
代表的な抗菌農産物洗浄剤組成物への、異なる酸の効果を比較するために試験を行った。この試験のために、乳酸、及び重硫酸ナトリウム(SAS)を使用した。試験した農産物洗浄剤組成物を以下の表に示す。
Claims (10)
- 以下の:
(a)少なくとも約25重量%の水;
(b)抗菌剤として陰イオン界面活性剤;
(c)シリコーンを含む消泡剤;
(d)酸味料;
(e)安定化剤;及び
(f)増粘剤、
を含む、単一相の水性低発泡性濃縮抗菌組成物であって、ここで、該組成物は、約50センチポアズ〜約3500センチポアズの粘度を有し、そして、前記増粘剤は、前記組成物が酸性条件下で相安定であるような有効量で存在する、前記組成物。 - 前記陰イオン界面活性剤が、以下の:アルキルスルフェート、アルキルスルホネート、アルキルアリールスルホネート、スルホン化脂肪酸、スルホン化脂肪酸エステル、スルホン化カルボン酸エステル、及びそれらの混合物から成る群から選ばれる、請求項1に記載の組成物。
- 前記組成物が、C5〜C11カルボン酸を実質的に含まない、請求項1に記載の組成物。
- 前記消泡剤が、ジメチルシリコーン、グリコールシロキサン、メチルフェノールポリシロキサン、トリアルキルシラン及びテトラアルキルシランからなる群から選ばれるシリコーン消泡剤を含む、請求項1に記載の組成物。
- 前記増粘剤が、以下の:天然ポリサッカライド又はセルロース増粘剤、植物滲出物、海草抽出物、水溶性ポリマー、ポリアクリル酸ベースの増粘剤、ポリアクリルアミドベースの増粘剤、無機質粘土ベースの増粘剤、及びそれらの混合物から成る群から選ばれる、請求項1に記載の組成物。
- 前記酸味料が食品添加物成分を含む、請求項1に記載の組成物。
- 前記酸味料が、以下の:クエン酸、重硫酸ナトリウム、酢酸、アジピン酸、酒石酸、プロピオン酸、リンゴ酸、乳酸、硫酸、並びにそれらの誘導体及び混合物から成る群から選ばれる、請求項1に記載の組成物。
- 前記組成物が、以下の:
約0.01重量%〜約50重量%の抗菌剤;
約0.01重量%〜約10.0重量%のシリコーンを含む消泡剤;
約0.1重量%〜約10重量%の増粘剤;及び
約1重量%〜約50重量%の酸味料、
を含む、請求項1に記載の組成物。 - 前記組成物が、約3.2未満のpHを有する、請求項1に記載の組成物。
- 前記組成物が、さらに、以下の:界面活性剤、加工助剤、染料、着色剤、付臭剤、及びそれらの混合物から成る群から選ばれる追加の成分を含む、請求項1に記載の組成物。
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Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20130344210A1 (en) * | 2011-05-25 | 2013-12-26 | Jones-Hamilton Co. | Food Treatment Method |
CN105377979B (zh) | 2013-07-12 | 2018-08-31 | 龙喜陆工业株式会社 | 抗病毒性氯乙烯系树脂组合物、内装片材及其制造方法、抗病毒性壁纸及其制造方法 |
JP6246512B2 (ja) * | 2013-07-12 | 2017-12-13 | ロンシール工業株式会社 | 抗ウイルス性壁紙 |
JP2015030947A (ja) * | 2013-08-05 | 2015-02-16 | ロンシール工業株式会社 | 抗ウイルス性壁紙 |
US9675067B2 (en) | 2014-09-03 | 2017-06-13 | Hawkins, Inc. | Animal feed preservative, supplement and methods |
JP6867743B2 (ja) * | 2014-11-27 | 2021-05-12 | ロンシール工業株式会社 | 抗ウイルス性を有する表面処理剤及び表面処理剤が塗布されている抗ウイルス性シート状物 |
AU2016377338B2 (en) * | 2015-12-22 | 2019-10-31 | 3M Innovative Properties Company | Methods for spore removal |
CA3054827C (en) | 2017-03-01 | 2023-02-14 | Ecolab Usa Inc. | Reduced inhalation hazard sanitizers and disinfectants via high molecular weight polymers |
CN106820791B (zh) * | 2017-03-28 | 2024-07-12 | 广东金丽声展示设备有限公司 | 一种超市用货架 |
AU2018342100B2 (en) | 2017-09-26 | 2021-08-12 | Ecolab Usa Inc. | Acidic/anionic antimicrobial and virucidal compositions and uses thereof |
JP2022502237A (ja) * | 2018-09-28 | 2022-01-11 | ダウ グローバル テクノロジーズ エルエルシー | ヒドロキシエチルセルロース誘導体泡制御剤および食材の加工方法 |
Family Cites Families (212)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA723264B (en) | 1972-10-13 | 1974-08-28 | H Van Til | Improvements in toys |
DE2327857C3 (de) | 1973-06-01 | 1982-04-29 | Henkel KGaA, 4000 Düsseldorf | Flüssiges schaumreguliertes Waschmittel |
IT1004032B (it) | 1973-11-16 | 1976-07-10 | Colgate Palmolive Co | Procedimento per la produzione di particelle da incorporare in denti frici per dare agli stessi un aspetto screziato particelle otte nute e dentifricio che le contiene |
AT338948B (de) | 1974-10-10 | 1977-09-26 | Henkel & Cie Gmbh | Pulverformige wasch- und reinigungsmittel und verfahren zu ihrer herstellung |
US4069312A (en) | 1974-11-04 | 1978-01-17 | Colgate Palmolive Company | Uniform particles of speckling material for incorporation in oral dentrifices |
US4069311A (en) | 1974-11-04 | 1978-01-17 | Colgate Palmolive Company | Oral dentifrice containing uniform particles of speckling material |
US4181621A (en) | 1975-07-08 | 1980-01-01 | Blendax-Werke R. Schneider & Co. | Cleaning agents for dentures |
DE2618977C3 (de) | 1976-04-29 | 1980-02-14 | Henkel Kgaa, 4000 Duesseldorf | Flüssiges, scheuernd wirkendes Reinigungsmittel |
DE2709690B1 (de) | 1977-03-05 | 1978-05-11 | Henkel Kgaa | Fluessiges Reinigungsmittel |
AT352241B (de) | 1977-04-22 | 1979-09-10 | Henkel Kgaa | Pulverfoermiges, phosphatfreies textil- waschmittel |
US4163795A (en) | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
US4163798A (en) | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
US4163796A (en) | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
US4190668A (en) | 1977-12-14 | 1980-02-26 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
US4163797A (en) | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
US4225669A (en) | 1979-04-27 | 1980-09-30 | Melnick Joseph L | Staining and analysis of bacteria |
US4228048A (en) | 1979-05-25 | 1980-10-14 | Chemed Corporation | Foam cleaner for food plants |
US4241080A (en) | 1979-05-29 | 1980-12-23 | The Dow Chemical Company | Stabilized aqueous antimicrobial composition |
US4232041A (en) | 1979-06-20 | 1980-11-04 | The Dow Chemical Company | Aqueous antimicrobial composition having improved stability |
GB2072014B (en) | 1980-03-08 | 1984-02-15 | Kanebo Ltd | Cosmetics containing 18-glycyrrhizins |
US4421665A (en) | 1980-08-25 | 1983-12-20 | Lloyd Eugene A | Contact lens cleaning composition containing lipid solvent and method of using |
US4654208A (en) | 1983-03-01 | 1987-03-31 | Stockel Richard F | Anti-microbial compositions comprising an aqueous solution of a germicidal polymeric nitrogen compound and a potentiating oxidizing agent |
US4485029A (en) | 1984-03-19 | 1984-11-27 | Minnesota Mining And Manufacturing Company | Disinfecting method and compositions |
US4826689A (en) | 1984-05-21 | 1989-05-02 | University Of Rochester | Method for making uniformly sized particles from water-insoluble organic compounds |
US4632847A (en) | 1985-02-06 | 1986-12-30 | Isotek Corporation | In situ polymeric membrane for isolating hazardous materials |
US5112750A (en) | 1985-06-25 | 1992-05-12 | Asama Chemical Co., Ltd. | Immobilized cells and culture method utilizing the same |
DE3533531A1 (de) | 1985-09-20 | 1987-04-02 | Henkel Kgaa | Reinigungsmittel fuer harte oberflaechen |
US4776974A (en) | 1986-03-17 | 1988-10-11 | Diversey Wyandotte Corporation | Stable antimicrobial sanitizing composition concentrates containing alkyl amine oxides |
US4715980A (en) | 1986-03-17 | 1987-12-29 | Diversey Wyandotte Corporation | Antimicrobial sanitizing composition containing n-alkyl and n-alkenyl succinic acid and methods for use |
GB8620845D0 (en) | 1986-08-28 | 1986-10-08 | Reckitt & Colmann Prod Ltd | Treatment of textile surfaces |
US5531982A (en) | 1987-01-30 | 1996-07-02 | Colgate Palmolive Company | Antimicrobial oral composition |
DE3711680A1 (de) | 1987-04-07 | 1988-10-27 | Hoechst Ag | Waessrige biozide kationische kunststoffdispersionen und deren verwendung als fungizide, bakterizide und algizide ausruestungsmittel |
US5128342A (en) | 1987-10-03 | 1992-07-07 | Globus Alfred R | Stable, active chlorine containing anti-microbial compositions |
US5087757A (en) | 1987-12-16 | 1992-02-11 | The Dow Chemical Company | Preparation of alkylthioethylamine salts |
DE3812693A1 (de) | 1988-03-19 | 1989-09-28 | Reckitt Gmbh | Reinigungstablette fuer zahnprothesen |
US4973466A (en) | 1988-06-21 | 1990-11-27 | Chiron Ophthalmics, Inc. | Wound-healing dressings and methods |
US4938763B1 (en) | 1988-10-03 | 1995-07-04 | Atrix Lab Inc | Biodegradable in-situ forming implants and method of producing the same |
US5186857A (en) | 1988-11-14 | 1993-02-16 | Imaginative Research Associates, Inc. | Self-foaming oil compositions and process for making and using same |
DE3904099C1 (ja) | 1989-02-11 | 1990-07-12 | Schuelke & Mayr Gmbh, 2000 Norderstedt, De | |
US5158766A (en) | 1989-04-13 | 1992-10-27 | Ecolab, Inc. | Storage stable aqueous soluble germicidal film forming composition |
US5116620A (en) | 1989-11-21 | 1992-05-26 | Bruce A. Barber | Antimicrobial wound dressing |
USRE37950E1 (en) | 1990-04-24 | 2002-12-31 | Atrix Laboratories | Biogradable in-situ forming implants and methods of producing the same |
DE4015859A1 (de) | 1990-05-17 | 1991-11-21 | Henkel Kgaa | Aktivatoren fuer anorganische perverbindungen |
US5158887A (en) | 1990-09-09 | 1992-10-27 | Hsu Edward J | Process for massive conversion of clostridia in synchronized cells of elongated length or refractile endospores |
US5143720A (en) | 1990-11-28 | 1992-09-01 | Microcide, Inc. | Disinfecting and sanitizing compositions |
US5288493A (en) | 1991-05-17 | 1994-02-22 | National Starch And Chemical Investment Holding Corporation | Skin care compositions with improved rub-off resistance |
US5234719A (en) | 1991-06-04 | 1993-08-10 | Ecolab Inc. | Food additive sanitizing compositions |
US5200189A (en) | 1991-07-23 | 1993-04-06 | Ecolab Inc. | Peroxyacid antimicrobial composition |
US5158772A (en) | 1991-09-23 | 1992-10-27 | Davis Walter B | Unique bacterial polysaccharide polymer gel in cosmetics, pharmaceuticals and foods |
IL101007A (en) | 1992-02-18 | 1997-08-14 | Pharmos Ltd | Dry stable compositions prepared by lyophilization |
MX9301789A (es) | 1992-04-03 | 1993-10-01 | Iaf Biochem Int | Nuevos oligopeptidos lipofilicos con actividad inmunomoduladora. |
US5270351A (en) | 1992-06-15 | 1993-12-14 | American Dental Association Health Foundation | Adhesion-promoting agents incorporating polyvalent cations |
US5436008A (en) | 1992-12-11 | 1995-07-25 | Ecolab Inc. | Sanitizing compositions |
US5403587A (en) | 1993-04-22 | 1995-04-04 | Eastman Kodak Company | Disinfectant and sanitizing compositions based on essential oils |
AU7564494A (en) | 1993-08-13 | 1995-03-14 | Smith & Nephew Richards Inc. | Microporous polymeric foams and microtextured surfaces |
US5370729A (en) | 1993-09-15 | 1994-12-06 | Ecolab Inc. | Food safe composition to facilitate soil removal |
US5639466A (en) | 1994-02-24 | 1997-06-17 | Chronopol, Inc. | Method for packaging foodstuffs |
US5731275A (en) | 1994-04-05 | 1998-03-24 | Universite De Montreal | Synergistic detergent and disinfectant combinations for decontaminating biofilm-coated surfaces |
GB9409466D0 (en) | 1994-05-12 | 1994-06-29 | Ciba Geigy Ag | Textile treatment |
US5939060A (en) | 1994-08-12 | 1999-08-17 | The Procter & Gamble Company | Composition for reducing malodor impression on inanimate surfaces |
US5510052A (en) | 1994-08-25 | 1996-04-23 | Colgate-Palmolive Co. | Enzymatic aqueous pretreatment composition for dishware |
US5540920A (en) | 1994-11-22 | 1996-07-30 | Olin Corporation | Synergistic biocide composition containing pyrithione plus an additive |
US5614538A (en) | 1994-12-05 | 1997-03-25 | Olin Corporation | Synergistic antimicrobial composition containing pyrithione and alcohol |
US5900445A (en) | 1994-12-20 | 1999-05-04 | Bic Corporation | Erasable ink composition containing a polymer dye obtained from ethylenic monomers and marking instrument containing same |
US5567753A (en) | 1995-01-27 | 1996-10-22 | Avery Dennison Corporation | Adhesive composition which changes from colored to colorless upon application to a substrate |
US5939203A (en) | 1995-02-03 | 1999-08-17 | Arch Chemicals, Inc. | Discoloration prevention in pyrithione-containing coating compositions |
US6777003B1 (en) | 1995-06-07 | 2004-08-17 | Cognis Corporation | Iodine complex of alkyl polyglycosides |
US5626856A (en) | 1995-06-30 | 1997-05-06 | Safe & Dry Company, Inc. | Cosmetic delivery vehicles and related compositions |
US5645823A (en) | 1995-07-07 | 1997-07-08 | Thrall; Bernice Eileen | Keratinous tissue conditioner |
US5736152A (en) | 1995-10-27 | 1998-04-07 | Atrix Laboratories, Inc. | Non-polymeric sustained release delivery system |
US5718895A (en) | 1995-11-16 | 1998-02-17 | Alcon Laboratories, Inc. | Enzymes with low isoelectric points for use in contact lens cleaning |
DE19600475A1 (de) | 1996-01-09 | 1997-07-10 | Henkel Ecolab Gmbh & Co Ohg | Verfahren zum Reinigen und Desinfizieren von Melkanlagen |
US6010993A (en) | 1996-02-23 | 2000-01-04 | The Procter & Gamble Company | Disinfecting compositions |
US20020169099A1 (en) | 1996-04-15 | 2002-11-14 | Stepan Company, A Corporation Of The State Of Delaware | High foaming detergent composition having a non-ionic surfactant base |
ATE203048T1 (de) | 1996-05-31 | 2001-07-15 | Ecolab Inc | Förderanlageschmiermittel auf basis von alkyletheramin |
US5723418A (en) | 1996-05-31 | 1998-03-03 | Ecolab Inc. | Alkyl ether amine conveyor lubricants containing corrosion inhibitors |
US6358897B1 (en) | 1996-06-07 | 2002-03-19 | Alcon Laboratories, Inc. | Alkyl trypsin compositions and methods of use in contact lens cleaning and disinfecting systems |
US6136885A (en) | 1996-06-14 | 2000-10-24 | 3M Innovative Proprerties Company | Glass ionomer cement |
US5868859A (en) | 1996-10-11 | 1999-02-09 | Ecolab Inc. | Use of infrared radiation in detection methods to defoam aqueous systems |
US6110883A (en) | 1996-11-13 | 2000-08-29 | The Procter & Gamble Company | Aqueous alkaline peroxygen bleach-containing compositions |
IL130709A0 (en) | 1996-12-31 | 2000-06-01 | American Medical Res Inc | Skin product having continuing antimicrobial antiviral antiseptic and healing properties |
US6242526B1 (en) | 1997-01-28 | 2001-06-05 | Stepan Company | Antimicrobial polymer latexes derived from unsaturated quaternary ammonium compounds and antimicrobial coatings, sealants, adhesives and elastomers produced from such latexes |
DE19713852A1 (de) | 1997-04-04 | 1998-10-08 | Henkel Kgaa | Aktivatoren für Persauerstoffverbindungen in Wasch- und Reinigungsmitteln |
AUPO690997A0 (en) | 1997-05-20 | 1997-06-12 | Novapharm Research (Australia) Pty Ltd | Alkylpolyglucosides containing disinfectant compositions active against pseudomonas microorganism |
US6183757B1 (en) | 1997-06-04 | 2001-02-06 | Procter & Gamble Company | Mild, rinse-off antimicrobial cleansing compositions which provide improved immediate germ reduction during washing |
US6183763B1 (en) | 1997-06-04 | 2001-02-06 | Procter & Gamble Company | Antimicrobial wipes which provide improved immediate germ reduction |
US6217887B1 (en) | 1997-06-04 | 2001-04-17 | The Procter & Gamble Company | Leave-on antimicrobial compositions which provide improved immediate germ reduction |
US6656923B1 (en) | 1997-06-09 | 2003-12-02 | The Procter & Gamble Company | Uncomplexed cyclodextrin compositions for odor and wrinkle control |
US6001343A (en) | 1997-06-09 | 1999-12-14 | The Procter & Gamble Company | Uncomplexed cyclodextrin compositions for odor and wrinkle control |
AU4356997A (en) | 1997-06-09 | 1998-12-30 | Procter & Gamble Company, The | Malodor reducing composition containing amber and musk materials |
US6762172B1 (en) | 1997-07-17 | 2004-07-13 | Nova Biogenetics, Inc. | Water-stabilized organosilane compounds and methods for using the same |
US6113815A (en) | 1997-07-18 | 2000-09-05 | Bioshield Technologies, Inc. | Ether-stabilized organosilane compositions and methods for using the same |
US6436444B1 (en) | 1997-09-26 | 2002-08-20 | Ecolab Inc. | Acidic aqueous chlorite teat dip providing shelf life sanitizing capacity and tissue protection |
US6749869B1 (en) | 1997-09-26 | 2004-06-15 | Ecolab | Acidic aqueous chlorite teat dip providing shelf life, sanitizing capacity and tissue protection |
US5916581A (en) | 1997-10-21 | 1999-06-29 | West Agro, Inc. | Iodine antimicrobial compositions containing nonionic surfactants and halogen anions |
US6139856A (en) | 1997-12-11 | 2000-10-31 | Biomedical Development Corp. | Composition useful for providing one-step surgical preparation and drape |
FR2774284B1 (fr) | 1998-02-03 | 2001-06-29 | Oreal | Poudre cosmetique et/ou dermatologique, son procede de preparation et ses utilisations |
ATE428301T1 (de) | 1998-02-12 | 2009-05-15 | Surfacine Dev Company Llc | Desinfektionzusammensetzungen mit verzögerter freisetzung der bioziden aktivität |
FR2776510B1 (fr) | 1998-03-31 | 2002-11-29 | Oreal | Derives de polyamino-acides et leur utilisation dans des compositions de traitement des fibres keratiniques |
US5980375A (en) | 1998-04-13 | 1999-11-09 | Chad Company Of Missouri, Inc. | Method and apparatus for antimicrobial treatment of animal carcasses |
US6528013B1 (en) | 1998-04-27 | 2003-03-04 | The Procter & Gamble Company | Uncomplexed cyclodextrin compositions for odor and wrinkle control |
US6440442B1 (en) | 1998-06-29 | 2002-08-27 | Hydromer, Inc. | Hydrophilic polymer blends used for dry cow therapy |
US6203812B1 (en) | 1998-06-29 | 2001-03-20 | Hydromer, Inc. | Hydrophilic polymer blends used to prevent cow skin infections |
US6395289B1 (en) | 1998-06-29 | 2002-05-28 | Hydromer, Inc. | Hydrophilic polymer blends used to prevent cow skin infections |
US6743574B1 (en) | 2000-09-12 | 2004-06-01 | Lifenet | Process for devitalizing soft-tissue engineered medical implants, and devitalized soft-tissue medical implants produced |
BR9908386A (pt) | 1998-07-17 | 2000-10-31 | Chemeq Ltd | Método de preparação de composições poliméricas, composições microbicidas, dermatológicas e/ou aditivas de alimentos para animais e seus usos |
US6010729A (en) | 1998-08-20 | 2000-01-04 | Ecolab Inc. | Treatment of animal carcasses |
US6235692B1 (en) | 1998-08-26 | 2001-05-22 | Cottrell International, Llc | Foaming enzyme spray cleaning composition and method of delivery |
JP3722268B2 (ja) | 1998-09-03 | 2005-11-30 | 栗田工業株式会社 | 抗菌性組成物 |
DK1123081T3 (da) | 1998-10-19 | 2003-03-24 | Synthes Ag | Hærdelig keramisk hydraulisk cement |
US5998358A (en) | 1999-03-23 | 1999-12-07 | Ecolab Inc. | Antimicrobial acid cleaner for use on organic or food soil |
US6534075B1 (en) | 1999-03-26 | 2003-03-18 | Ecolab Inc. | Antimicrobial and antiviral compositions and treatments for food surfaces |
US6488943B1 (en) | 1999-04-13 | 2002-12-03 | The Procter & Gamble Company | Antimicrobial wipes which provide improved immediate germ reduction |
US6506803B1 (en) | 1999-04-28 | 2003-01-14 | Regents Of The University Of Michigan | Methods of preventing and treating microbial infections |
US6313182B1 (en) | 1999-05-04 | 2001-11-06 | Air Products And Chemicals, Inc. | Acetylenic diol ethylene oxide/propylene oxide adducts and processes for their manufacture |
JP4874483B2 (ja) | 1999-06-09 | 2012-02-15 | ロバート イー. シーバース | 超臨界流体補助ネブライゼーション及びバブル乾燥 |
EP1198179B1 (en) | 1999-07-22 | 2007-01-17 | Astaris Llc | Antimicrobial polyphosphates in food processing |
US7384895B2 (en) | 1999-08-16 | 2008-06-10 | Ecolab Inc. | Conveyor lubricant, passivation of a thermoplastic container to stress cracking and thermoplastic stress crack inhibitor |
DE19942536A1 (de) | 1999-09-07 | 2001-03-08 | Henkel Ecolab Gmbh & Co Ohg | Verwendung von Schmiermitteln auf Polysiloxan-Basis |
DE19942534A1 (de) | 1999-09-07 | 2001-03-08 | Henkel Ecolab Gmbh & Co Ohg | Fluorhaltige Schmiermittel |
US6343225B1 (en) | 1999-09-14 | 2002-01-29 | Implanted Biosystems, Inc. | Implantable glucose sensor |
US6716805B1 (en) | 1999-09-27 | 2004-04-06 | The Procter & Gamble Company | Hard surface cleaning compositions, premoistened wipes, methods of use, and articles comprising said compositions or wipes and instructions for use resulting in easier cleaning and maintenance, improved surface appearance and/or hygiene under stress conditions such as no-rinse |
US6235820B1 (en) | 1999-10-12 | 2001-05-22 | Air Products And Chemicals, Inc. | Alkylated aminoalkylpiperazine surfactants |
US6281170B1 (en) | 1999-10-18 | 2001-08-28 | Air Products And Chemicals, Inc. | Surface tension reduction with N,N,N'-trialkkyl ureas |
US7012053B1 (en) | 1999-10-22 | 2006-03-14 | The Procter & Gamble Company | Fabric care composition and method comprising a fabric care polysaccharide and wrinkle control agent |
US6369146B1 (en) | 1999-10-26 | 2002-04-09 | Air Products And Chemicals, Inc. | Malic acid diester surfactants |
US6258342B1 (en) | 1999-11-03 | 2001-07-10 | Hercules Incorporated | Process for making toothpaste using agglomerated dispersible polymers |
US6461631B1 (en) | 1999-11-16 | 2002-10-08 | Atrix Laboratories, Inc. | Biodegradable polymer composition |
EP1231838B1 (en) | 1999-11-24 | 2009-12-02 | 3M Innovative Properties Company | Fruit, vegetable, and seed disinfectants |
AU1956401A (en) | 1999-12-10 | 2001-06-18 | Microban Products Company | Antimicrobial synthetic ion exchange resins |
US6716895B1 (en) | 1999-12-15 | 2004-04-06 | C.R. Bard, Inc. | Polymer compositions containing colloids of silver salts |
US6319526B1 (en) | 2000-01-06 | 2001-11-20 | Land O'lakes, Inc. | Pasta filata cheese |
US6463766B2 (en) | 2000-01-28 | 2002-10-15 | Kabushiki Kaisha Toshiba | Washing machine with means for preventing propagation of microorganism |
CA2397496C (en) | 2000-02-28 | 2007-07-24 | The Procter & Gamble Company | Acidic antimicrobial compositions for treating food and food contact surfaces and methods of use thereof |
US6506737B1 (en) | 2000-04-05 | 2003-01-14 | Ecolab, Inc. | Antimicrobial phosphonium and sulfonium polyhalide compositions |
US6423376B1 (en) | 2000-04-06 | 2002-07-23 | Air Products And Chemicals, Inc. | Tartaric acid diesters as biodegradable surfactants |
US6342470B1 (en) | 2000-04-26 | 2002-01-29 | Unilever Home & Personal Care Usa | Bar comprising soap, fatty acid, polyalkylene glycol and protic acid salts in critical ratios and providing enhanced skin care benefits |
US6218348B1 (en) | 2000-04-26 | 2001-04-17 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Process of making soap bar with enhanced skin benefits comprising adding salts of specific protic acid |
DE60114174T2 (de) | 2000-04-28 | 2006-07-20 | Ecolab Inc., St. Paul | Antimikrobielle zusammensetzung |
US6593283B2 (en) | 2000-04-28 | 2003-07-15 | Ecolab Inc. | Antimicrobial composition |
US6537563B2 (en) | 2000-05-11 | 2003-03-25 | Jeneric/Pentron, Inc. | Dental acid etchant composition and method of use |
US7282211B2 (en) | 2001-05-21 | 2007-10-16 | Btg International Inc. | Pest treatment composition |
US6511962B1 (en) | 2000-07-17 | 2003-01-28 | Micrologix Biotech Inc. | Derivatives of laspartomycin and preparation and use thereof |
US6306463B1 (en) | 2000-07-20 | 2001-10-23 | Air Products And Chemicals, Inc. | Citric acid tri-alkylamide surfactants |
US7097705B2 (en) | 2000-09-11 | 2006-08-29 | Air Products And Chemicals, Inc. | Cationic-anionic blends for dynamic surface tension reduction |
US6432436B1 (en) | 2000-10-03 | 2002-08-13 | Musculoskeletal Transplant Foundation | Partially demineralized cortical bone constructs |
US6617294B2 (en) | 2000-10-20 | 2003-09-09 | Vinod K. Narula | Waterless sanitizing hand cleanser |
US20020132742A1 (en) | 2000-12-06 | 2002-09-19 | Mizuki Peter Y. | Composition for cleaning fruits, vegetables and food contact surfaces |
US6514556B2 (en) * | 2000-12-15 | 2003-02-04 | Ecolab Inc. | Method and composition for washing poultry during processing |
US6699825B2 (en) | 2001-01-12 | 2004-03-02 | S.C. Johnson & Son, Inc. | Acidic hard-surface antimicrobial cleaner |
JP3936143B2 (ja) | 2001-02-06 | 2007-06-27 | 憲司 中村 | 抗菌防臭性の化粧用ブラシとその製造方法 |
DE10109217A1 (de) | 2001-02-26 | 2002-09-05 | Mitsubishi Polyester Film Gmbh | Transparente, biaxial orientierte Polyesterfolie |
US6413914B1 (en) | 2001-03-29 | 2002-07-02 | Air Products And Chemicals, Inc. | Low foam N,N′-dialkylmalamide wetting agents |
US6399543B1 (en) | 2001-03-29 | 2002-06-04 | Air Products And Chemicals, Inc. | Low foam N,N′-dialkyltartaramide wetting agents |
AU766539B2 (en) | 2001-04-20 | 2003-10-16 | Evonik Goldschmidt Gmbh | Compositions for controlling microorganisms, comprising an effective content of enzymatically prepared esters of polyglycerol |
US6929705B2 (en) | 2001-04-30 | 2005-08-16 | Ak Steel Corporation | Antimicrobial coated metal sheet |
US6537577B1 (en) | 2001-06-04 | 2003-03-25 | Bio Medical Development Corporation | Method of prophylaxis for bovine mastitis |
FR2826270B1 (fr) | 2001-06-22 | 2005-01-28 | Oreal | Lingette et ses utilisations dans le domaine cosmetique |
WO2003003832A1 (en) | 2001-07-06 | 2003-01-16 | Rnl Life Science Ltd. | Acid disinfectant composition comprising an anion surfactant |
US6979455B2 (en) | 2001-07-10 | 2005-12-27 | Microban Products Company | Antimicrobial concentrates |
US6627593B2 (en) | 2001-07-13 | 2003-09-30 | Ecolab Inc. | High concentration monoester peroxy dicarboxylic acid compositions, use solutions, and methods employing them |
US6573102B2 (en) | 2001-07-27 | 2003-06-03 | Coulter International Corp. | Lytic reagent composition for determination of nucleated blood cells |
WO2003014284A1 (en) | 2001-08-07 | 2003-02-20 | Fmc Corporation | High retention sanitizer systems |
US7256167B2 (en) | 2001-08-31 | 2007-08-14 | Reckitt Benckiser Inc. | Hard surface cleaner comprising suspended particles and oxidizing agent |
JP2003073229A (ja) | 2001-09-03 | 2003-03-12 | Asahi Kasei Corp | セルロースを含有するスプレー剤 |
DE10146264A1 (de) | 2001-09-20 | 2003-04-17 | Ecolab Gmbh & Co Ohg | Verwendung von O/W-Emulsionen zur Kettenschmierung |
US6762208B2 (en) | 2001-10-01 | 2004-07-13 | Air Products And Chemicals, Inc. | Alkane diol foam controlling agents |
US6824802B2 (en) | 2001-10-02 | 2004-11-30 | Nestec S.A. | On-demand neutralization of acid-preserved food |
JP2005505660A (ja) | 2001-10-09 | 2005-02-24 | ザ プロクター アンド ギャンブル カンパニー | ポリマービグアニドを含む表面処理用予備湿潤拭き取り用品 |
US7468105B2 (en) | 2001-10-16 | 2008-12-23 | Micron Technology, Inc. | CMP cleaning composition with microbial inhibitor |
EP2082724B1 (en) | 2001-11-15 | 2013-08-21 | Laboratorios Miret, S.A. | Use of cationic surfactant as antimicrobial activity enhancer in deodorants and oral care |
GB2383334A (en) | 2001-12-20 | 2003-06-25 | Reckitt Benckiser Inc | Powder detergent compositions |
GB2384244B (en) | 2002-01-18 | 2004-03-24 | Reckitt Benckiser | Cleaning compositions and uses |
US7008979B2 (en) | 2002-04-30 | 2006-03-07 | Hydromer, Inc. | Coating composition for multiple hydrophilic applications |
US7067499B2 (en) | 2002-05-06 | 2006-06-27 | Hercules Incorporated | Cationic polymer composition and its use in conditioning applications |
US7097850B2 (en) | 2002-06-18 | 2006-08-29 | Surmodics, Inc. | Bioactive agent release coating and controlled humidity method |
US7569530B1 (en) | 2003-06-20 | 2009-08-04 | The Procter & Gamble Company | Antimicrobial compositions, products and methods employing same |
DE10227872A1 (de) | 2002-06-22 | 2004-01-08 | Ecolab Gmbh & Co. Ohg | Wässriges Konzentrat zur Desinfektion von Oberflächen |
WO2004000234A2 (en) | 2002-06-25 | 2003-12-31 | Wm. Wrigley Jr. Company | Breath freshening and oral cleansing product with cinnamaldehyde |
KR100532097B1 (ko) | 2002-08-28 | 2005-11-29 | 삼성전자주식회사 | 수용성 고분자 항균처리제 및 이를 포함하는 잉크 조성물 |
US6962608B1 (en) | 2002-10-01 | 2005-11-08 | The Regents Of The University Of California | Regenerable antimicrobial polymers and fibers with oxygen bleaches |
US7001632B2 (en) | 2003-03-03 | 2006-02-21 | Kraft Foods Holdings, Inc. | Anti-listeria compositions for use in food products |
US7087190B2 (en) | 2003-03-20 | 2006-08-08 | Ecolab Inc. | Composition for the production of chlorine dioxide using non-iodo interhalides or polyhalides and methods of making and using the same |
US6953507B2 (en) | 2003-03-21 | 2005-10-11 | Ecolab Inc. | Low temperature cleaning |
US20050129643A1 (en) | 2003-06-20 | 2005-06-16 | Lepilleur Carole A. | Hydrocolloids and process therefor |
US7468346B2 (en) | 2003-06-30 | 2008-12-23 | Ecolab Inc. | Low foaming washing liquid |
US7491753B2 (en) | 2003-07-03 | 2009-02-17 | Mallard Creek Polymers, Inc. | Antimicrobial and antistatic polymers and methods of using such polymers on various substrates |
BRPI0416387A (pt) | 2003-11-11 | 2007-02-21 | Veckis Ind Ltd | composição desinfetante e métodos de confecção e uso da mesma |
US8226888B2 (en) | 2003-12-22 | 2012-07-24 | Institute For Environmental Health, Inc. | Adherent antimicrobial barrier and sanitizing agent |
US7771737B2 (en) * | 2004-01-09 | 2010-08-10 | Ecolab Inc. | Medium chain peroxycarboxylic acid compositions |
AU2005206690B2 (en) | 2004-01-09 | 2010-09-23 | Ecolab Inc. | Medium chain peroxycarboxylic acid compositions |
US7507429B2 (en) * | 2004-01-09 | 2009-03-24 | Ecolab Inc. | Methods for washing carcasses, meat, or meat products with medium chain peroxycarboxylic acid compositions |
US7135449B2 (en) | 2004-02-20 | 2006-11-14 | Milliken & Company | Composition for removal of odors and contaminants from textiles and method |
US7014843B2 (en) | 2004-03-24 | 2006-03-21 | Reheis, Inc. | Enhanced efficacy basic aluminum halides/metal cation salt, antiperspirants actives and compositions containing such materials and methods for making |
GB2419888B (en) | 2004-11-06 | 2010-04-14 | St Giles Foods Ltd | Liquid edible products and methods of stabilising liquid edible products |
EP1824954A1 (en) | 2004-11-19 | 2007-08-29 | The Procter and Gamble Company | Acidic laundry detergent compositions |
DE102004062775A1 (de) | 2004-12-21 | 2006-06-29 | Stockhausen Gmbh | Alkoholischer Pumpschaum |
US20060204466A1 (en) | 2005-03-08 | 2006-09-14 | Ecolab Inc. | Hydroalcoholic antimicrobial composition with skin health benefits |
MX2007010908A (es) | 2005-03-10 | 2007-12-05 | 3M Innovative Properties Co | Composiciones antimicrobianas que comprenden esteres de acidos hidroxicarboxilicos. |
US7112559B1 (en) | 2005-03-14 | 2006-09-26 | Ecolab Inc. | Thickened quaternary ammonium compound sanitizer |
US7309684B2 (en) | 2005-05-12 | 2007-12-18 | The Lubrizol Corporation | Oil-in-water emulsified remover comprising an ethoxylated alcohol surfactant |
US20080274242A1 (en) | 2006-07-21 | 2008-11-06 | Ecolab Inc. | Antimicrobial compositions and methods for treating packaged food products |
CA2611784C (en) | 2005-07-25 | 2014-09-16 | Ecolab Inc. | Antimicrobial compositions for use on food products |
EP2255665B1 (en) | 2005-07-25 | 2019-11-20 | Ecolab USA Inc. | Antimicrobial compositions and methods for treating packaged food products |
US20070042094A1 (en) | 2005-08-22 | 2007-02-22 | Alcide Corporation | Oxidation method and compositions therefor |
AU2006283215B2 (en) | 2005-08-23 | 2012-11-22 | 3M Innovative Properties Company | Methods of applying antimicrobial formulations on food |
US20070048344A1 (en) | 2005-08-31 | 2007-03-01 | Ali Yahiaoui | Antimicrobial composition |
WO2007064519A1 (en) | 2005-12-02 | 2007-06-07 | Gic Innovations Company | Vehicles for oral care with magnolia bark extract |
CA2644674A1 (en) | 2006-03-13 | 2007-09-20 | Vicente Etayo Garralda | Biodegradable protein based thermoset compositions, preparation methods and applications thereof |
US20080075793A1 (en) | 2006-09-21 | 2008-03-27 | Dunshee Wayne K | Antiviral compositions and methods of use |
KR101540220B1 (ko) | 2006-10-27 | 2015-07-29 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 식품용 증점제 조성물 |
US9555167B2 (en) | 2006-12-11 | 2017-01-31 | 3M Innovative Properties Company | Biocompatible antimicrobial compositions |
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CA2794841C (en) | 2021-02-23 |
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EP2571383A2 (en) | 2013-03-27 |
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