DK160103B - CLEANER BASED ON ACTIVE CHLOR AND ALKALI - Google Patents

CLEANER BASED ON ACTIVE CHLOR AND ALKALI Download PDF

Info

Publication number
DK160103B
DK160103B DK172184A DK172184A DK160103B DK 160103 B DK160103 B DK 160103B DK 172184 A DK172184 A DK 172184A DK 172184 A DK172184 A DK 172184A DK 160103 B DK160103 B DK 160103B
Authority
DK
Denmark
Prior art keywords
alkali
active chlorine
active
chlor
compound
Prior art date
Application number
DK172184A
Other languages
Danish (da)
Other versions
DK160103C (en
DK172184A (en
DK172184D0 (en
Inventor
Nicolaas Andrianus Ign Paassen
Original Assignee
Stamicarbon
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Stamicarbon filed Critical Stamicarbon
Publication of DK172184D0 publication Critical patent/DK172184D0/en
Publication of DK172184A publication Critical patent/DK172184A/en
Publication of DK160103B publication Critical patent/DK160103B/en
Application granted granted Critical
Publication of DK160103C publication Critical patent/DK160103C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/06Ether- or thioether carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions

Landscapes

  • 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)

Description

- i -- i -

DK 160103 BDK 160103 B

Opfindelsen angår et rensemiddel baseret på aktivt chlor og alkali. Sådanne rensemidler anvendes 1 praksis til rensning af rør og kanaler o.l., fx. 1 apparater til mælkebehandling. Normalt finder rensningen sted ved 40°C - 45°C og derfor skal blandingen forvarmes til en 5 passende temperatur. Normalt anvendes der ikke andre overfladeaktive stoffer end befugtningsmldler 1 sådanne blandinger, fordi der ellers ville forekomme for megen skumdannelse, især ved forhøjede temperatuer og intens mekanisk behandling, hvilket følgelig ville påvirke rensningen snarere i en uheldig retning end på en fordelagtig måde.The invention relates to a cleaning agent based on active chlorine and alkali. Such cleaners are used in practices for cleaning pipes and ducts and the like, e.g. 1 milk processing apparatus. Usually the purification takes place at 40 ° C - 45 ° C and therefore the mixture must be preheated to a suitable temperature. Normally, surfactants other than wetting agents in such mixtures are not used because otherwise there would be too much foaming, especially at elevated temperatures and intense mechanical treatment, which would consequently affect the cleaning rather in an unfortunate direction than in an advantageous way.

10 Sådanne rensemidler er meget forskellige fra de såkaldte fortykkede blegemidler, som fx. nævnt i GB-offentliggørelsesskrift 207610 og EP-offentliggørelsesskrift 0.072.600, som indeholder meget mere hypo-chloritopløsning end alkali (se side 2, linie 25 1 EP-offentliggørel-sesskrift 0.072.600), og hvori det tilsatte overfladeaktive stof tjener 15 til fortykkelse af forbindelsen. De foreliggende forbindelser skal anvendes industrielt og indeholder al kalimetal hydroxider 1 en mængde på mindst 50% af blegningsmidlet.Such cleansers are very different from the so-called thickened bleaching agents, such as e.g. mentioned in GB Publication No. 207610 and EP Publication No. 0.072,600, which contains much more hypochlorite solution than alkali (see page 2, line 25 1 EP Publication No. 0.072,600), wherein the added surfactant serves 15 to thickening of the compound. The present compounds are to be used industrially and contain all potassium hydroxides in an amount of at least 50% of the bleaching agent.

Det har på overraskende måde vist sig, at en meget begrænset gruppe ethercarboxylsyrederi vater, når de tilsættes denne slags midler, har 20 en kombination af en meget effektiv overfladeaktiv virkning og en lav skumdannelse, hvilket gør det muligt at anvende disse forbindelser 1 de foreliggende rensemidler, og derpå at anvende disse rensemidler ved stuetemperatur. Der opnås derfor en vigtig energibesparelse på denne måde, der Ikke sker på bekostning af rensevirkningen.Surprisingly, it has been found that, when added to these agents, a very limited group of ether carboxylic acid preparations have a combination of a very effective surfactant and a low foaming, which allows these compounds to be used in the present cleaning agents. , and then using these cleaners at room temperature. Therefore, an important energy saving is achieved in this way, which is not at the expense of the cleaning effect.

25 Den foreliggende opfindelse angår derfor rensemidler på basis af aktivt chlor og alkali, der er karakteriseret ved, at de også indeholder en mindre mængde af en forbindelse med formlen: c«Hi70"(C2H*°)nCH2C00M, 30 hvor M er natrium eller kalium og n er er et tal, som har en gennemsnitsværdi mellem 1 og 10.The present invention therefore relates to active chlorine and alkali cleaners characterized in that they also contain a minor amount of a compound of the formula: c "Hi70" (C2H + °) nCH2C00M, where M is sodium or potassium and n is a number having an average value between 1 and 10.

De foreliggende overfladeaktive stoffer er kendt 1 sig selv og tilhører en gruppe forbindelser, som allerede har været kendt gennem 35 længere tid for dets anvendelighed. Inden for denne gruppe forbindelser - 2 - ΓΛ\/ Λ / r\ -1 Γ· 7 D 'The present surfactants are known in themselves and belong to a group of compounds which have been known for a long time for its usefulness. Within this group of connections - 2 - ΓΛ \ / Λ / r \ -1 Γ · 7 D '

Ur\ ; :, ; 1.1 ; DUr \; :,; 1.1; D

har C H -forbindelserne imidlertid altid varet betragtet som en slags 8 17 grænsetilfælde, og forbindelser udviklet fra mere langkædede hydrofobi-ske grupper blev altid foretrukket. Dette fremgår ikke blot at det ovennævnte GB-offentliggørelsesskrift 2.076.010, som, skønt det nævner, 5 at den hydrofobiske gruppe kan være fx. en Cg_20 alkyl gruppe, foretrækker C - C , og fra EP-offentliggørelsesskrift 0.072.600, der som hydrofobisk gruppe bl.a. nævner en alkylgruppe på 8 - 18 kulstofatomer og foretrækker Cl2 - Cig, men også fra NL-offentliggørelsesskrift 7405231, hvor den hydrofobiske gruppe igen kan være en Cg - C20 al kyl -10 gruppe, men atter foretrækkes C12- Cift-alkyl, og fra FR-offentliggørel-sesskrift 1.099.847, som, skønt der nævnes en C H „ forbindelse som et eksempel på en mulig forbindelse, også klart foretrækker større al kyl -forbindelser. Det skal bemærkes, at Cg-forbindelsen ikke anvendes i nogle af eksemlerne i de ovennævnte skrifter.however, the C H compounds have always been considered a kind of boundary case, and compounds developed from more long chain hydrophobic groups were always preferred. This is not only apparent from the aforementioned GB Publication No. 2,076,010, which, although it mentions that the hydrophobic group may be e.g. a Cg-20 alkyl group, prefers C - C, and from EP Publication specification 0.072,600 which, as a hydrophobic group, i. mentions an alkyl group of 8 to 18 carbon atoms and prefers Cl 2 -Cig, but also from NL Publication No. 7405231, wherein the hydrophobic group may again be a C 8 -C 20 alkyl group -10 but again C 12 -Cift alkyl is preferred and FR Publication 1,099,847, which, although mentioning a CH₂ compound as an example of a possible compound, also clearly prefers larger alkyl compounds. It should be noted that the Cg compound is not used in some of the examples in the aforementioned writings.

15 I forbindelserne, som anvendes ifølge den foreliggende opfindelse kan alkylgruppen C.H,, være en lige kæde eller en forgrenet gruppe, fx. n-octyl eller 2-ethyl hexyl. I princippet kan man selvfølgelig også blande den frie syre i forbindelsen, som indeholder det aktive chlor og alkali, således at det ønskede salt dannes in situ. Teoretisk er det 20 selvfølgelig også muligt at anvende andre salte, som fx. ammoniumsalte eller organiske ammonium- og aminsalte, men i praksis anvender man for- i trinsvis et salt af ethercarboxylsyre med samme anion som i al kalimetal hydroxidforbindelsen i basisblandingen.In the compounds used in the present invention, the alkyl group C H 2 may be a straight chain or a branched group, e.g. n-octyl or 2-ethyl hexyl. In principle, of course, the free acid can also be mixed in the compound containing the active chlorine and alkali, so that the desired salt is formed in situ. Theoretically, it is of course also possible to use other salts, such as e.g. ammonium salts or organic ammonium and amine salts, but in practice a salt of ether carboxylic acid with the same anion is used, preferably with the same anion as in all the potassium hydroxide compound in the base mixture.

De andre komponenter i systemet er de sædvanlige til denne slags 25 forbindelser. Alkaliet er Κ0Η eller NaOH og koncentrationen af det kan varieres indenfor relativt store grænser, i almindelighed mellem 20 -250 gram/1. En passende koncentration er i størrelsesordenen 80 - 120 g/1. Det aktive chlor i systemet kan udledes fra forskellige kendte forbindelser. Chorholdigt blegningslud er et billigt produkt og anven-30 des derfor i almindelighed. En forbindelse som trichlorcyanursyre eller chloramin T kan imidlertid også anvendes som et chlorproducerende mid del. Sædvanligvis indeholder systemet omkring 3% - 6% aktivt chlor, fortrinsvis omkring 4,5%. Som allerede nævnt er mængden af alkali i et sådant system mindst 50% af mængden af blegningsmiddel.The other components of the system are the usual ones for this kind of connection. The alkali is Κ0Η or NaOH and the concentration of it can be varied within relatively large limits, generally between 20-250 grams / l. A suitable concentration is in the order of 80-120 g / l. The active chlorine in the system can be derived from various known compounds. Chlorine bleaching liquor is a cheap product and is therefore generally used. However, a compound such as trichlorocyanuric acid or chloramine T can also be used as a chlorine-producing agent. Usually, the system contains about 3% - 6% of active chlorine, preferably about 4.5%. As already mentioned, the amount of alkali in such a system is at least 50% of the amount of bleach.

35 Mængden af overfladeaktivt stof, som skal anvendes ifølge den fo- - 3 - DK -of Μ" 3 religgende opfindelse kan bedst udtrykkes i vægtforholdet mellem overfladeaktivt stof og aktivt chlor. Dette vægtforhold kan i almindelighed variere fra 1:10 til 1:3. Således er det passende at anvende 0.65% af det foreliggende overfladeaktive stof ved den ovenævnte foretrukne 5 mængde på 4,5% af aktivt chlor.The amount of surfactant to be used in accordance with the present invention can best be expressed in the weight ratio of surfactant to active chlorine. This weight ratio can generally range from 1:10 to 1: 3. Thus, it is convenient to use 0.65% of the present surfactant at the above preferred amount of 4.5% of active chlorine.

EKSEMPLEREXAMPLES

Et antal blandinger blev fremstillet hver indeholdende 30% hypo-10 chlorit-blegemiddel (150 g chlor/1), 20% af en 50% vandig kaliumhydroxid, de procentvise mængder af ethercarboxylkaliumsal te anført 1 det følgende, og resten vand. De anvendte ethercarboxylsal te havde formlen octyl-0-(C2H40)nCH2C00K.A number of mixtures were prepared each containing 30% hypo-10 chlorite bleach (150 g chlorine / l), 20% of a 50% aqueous potassium hydroxide, the percentages of ether carboxyl potassium salt listed in the following, and the remainder water. The ether carboxyl salts used had the formula octyl-O- (C 2 H 40) nCH 2 CO.

Eksempel I II III IV V VI VII VIII IX X XIExample I II III IV V VI VII VIII IX X XI

% n « 3 0,5 1 0,75 0,5 0,5 0,25 0,4 - - 0,25 - % n * 5 - - 0,75 0,5 - 0,5 0,4 - - 0,25 0,65 % n * 8 1 0,5 - - 0,25 - - 0,60 0,65 0,25 -% n «3 0.5 1 0.75 0.5 0.5 0.25 0.4 - 0.25 -% n * 5 - 0.75 0.5 - 0.5 0.4 - - 0.25 0.65% n * 8 1 0.5 - - 0.25 - - 0.60 0.65 0.25 -

En skumdannelsesundersøgelse blev udført ved at opløse 10 g af 15 hvert produkt i 1 liter vand fra vandhanen (Tysk hårdhed omkring 20°), og at ryste 50 ml af denne opløsning kraftigt i hånden i en rystecylinder på 100 ml, og at aflæse skumvoluminet efter 1 minut. I dette eksperiment betragtes et skumvolumen på 15 ml eller mindre som tilfredsstillende. Resultaterne af disse eksperimenter er anført i den følgende 20 tabel.A foaming study was performed by dissolving 10 g of 15 each product in 1 liter of tap water (German hardness about 20 °), vigorously shaking 50 ml of this solution in a 100 ml shaking cylinder and reading the foam volume after 1 minute. In this experiment, a foam volume of 15 ml or less is considered satisfactory. The results of these experiments are given in the following table.

Γ',Ι/ *ί ,- Γ5 /-I ν Ο UΓ\ . < 1 ./ ; >1 Ο Ο - 4 - EKSEMPEL TEMPERATUR, °C ml skum I 20 10 II 20 12 _III_20_13_ IV 20 12 V 15 8 _VI_15_9_ VII 13 6 VIII 13 7 _IX_12_9_ 13 7 14 9 _19 _5_ 20 6 X 13 13 _XI_12_9_ 20 7Γ ', Ι / * ί, - Γ5 / -I ν Ο UΓ \. <1 ./; > 1 Ο Ο - 4 - EXAMPLE TEMPERATURE, ° C ml foam I 20 10 II 20 12 _III_20_13_ IV 20 12 V 15 8 _VI_15_9_ VII 13 6 VIII 13 7 _IX_12_9_ 13 7 14 9 _19 _5_ 20 6 X 13 13 _XI_12_9_ 20 7

Til nogle formål foretrækkes KOH i denne slags forbindelser og til andre formål foretrækkes NaOH. Dette udgør ingen forskel for virkningen af den foreliggende opfindelse, hvilket vil fremgå af de følgende to eksempler.For some purposes, KOH is preferred in these kinds of compounds and for other purposes NaOH is preferred. This makes no difference to the effect of the present invention, as will be apparent from the following two examples.

5 Blandingerne fra eksemplerne IX og XI blev atter fremstillet, men denne gang med natriumhydroxid. Disse blandinger betegnes med eksemplerne IXa og Xla. De blev også underkastet den ovennævnte skumdannelsesundersøgelse, ved 12°C og 20°C. Resultaterne er anført i det følgende og af hensyn til overskueligheden er de tilsvarende resultater med 10 kaliumhydroxid fra den ovenstående tabel atter anført her.The mixtures of Examples IX and XI were again prepared, but this time with sodium hydroxide. These mixtures are denoted by Examples IXa and Xla. They were also subjected to the above foam formation study, at 12 ° C and 20 ° C. The results are set out below and for reasons of clarity, the corresponding results with 10 potassium hydroxide from the above table are listed again.

- 5 -- 5 -

EKSEMPEL ml skum v 12°C ml skum v 20°CEXAMPLE ml foam at 12 ° C ml foam at 20 ° C

IX 9 6 IXa 10 7 XI 10 7 XIa 11 6IX 9 6 IXa 10 7 XI 10 7 XIa 11 6

Claims (3)

1 Rensemiddel baseret på aktivt chlor, som blegningsmiddel og alkalimetal hydroxider i en mængde på mindst 50¾ af blegningsmidlet, kendetegnet ved, at det indeholder en mindre mængde af en lavt-skummende forbindelse med formlen: 5 c.Hi,°-(cA°)nCH2C00M’ hvor M er natrium eller kalium og n er er et tal, som har en gennemsnitsværdi mellem 1 og 10.1 Active chlorine based detergent such as bleaching agent and alkali metal hydroxides in an amount of at least 50¾ of the bleaching agent, characterized in that it contains a minor amount of a low-foaming compound of the formula: 5 c.Hi, ° - (cA °) nCH2C00M 'where M is sodium or potassium and n is a number having an average value between 1 and 10. 2. Rensemiddel ifølge krav 1, kendetegnet ved, at vægtforholdet mellem den lavtskummende forbindelse og det aktive chlor er 1:10 til 1:3.Purifier according to claim 1, characterized in that the weight ratio of the low foaming compound to the active chlorine is 1:10 to 1: 3. 3. Rensemiddel ifølge krav 1 eller 2, kendetegnet ved, at det indeholder 3% - 6% aktivt chlor i form af en blegningslud. 15A cleaning agent according to claim 1 or 2, characterized in that it contains 3% - 6% of active chlorine in the form of a bleaching liquor. 15
DK172184A 1983-03-31 1984-03-29 CLEANER BASED ON ACTIVE CHLOR AND ALKALI DK160103C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL8301168A NL8301168A (en) 1983-03-31 1983-03-31 CLEANER BASED ON ACTIVE CHLORINE AND ALKALI.
NL8301168 1983-03-31

Publications (4)

Publication Number Publication Date
DK172184D0 DK172184D0 (en) 1984-03-29
DK172184A DK172184A (en) 1984-10-01
DK160103B true DK160103B (en) 1991-01-28
DK160103C DK160103C (en) 1991-06-10

Family

ID=19841642

Family Applications (1)

Application Number Title Priority Date Filing Date
DK172184A DK160103C (en) 1983-03-31 1984-03-29 CLEANER BASED ON ACTIVE CHLOR AND ALKALI

Country Status (5)

Country Link
EP (1) EP0121286B1 (en)
CA (1) CA1222427A (en)
DE (1) DE3479037D1 (en)
DK (1) DK160103C (en)
NL (1) NL8301168A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4670372A (en) * 1984-10-15 1987-06-02 Petrarch Systems, Inc. Process of developing radiation imaged photoresist with alkaline developer solution including a carboxylated surfactant
CA1281578C (en) * 1985-07-18 1991-03-19 Susan A. Ferguson High contrast photoresist developer with enhanced sensitivity
US7037884B2 (en) 1994-02-23 2006-05-02 Ecolab Inc. Alkaline cleaners based on alcohol ethoxy carboxylates
WO1995023202A1 (en) * 1994-02-23 1995-08-31 Ecolab Inc. Alkaline cleaners based on alcohol ethoxy carboxylates
DE19926627A1 (en) * 1999-06-11 2000-12-14 Henkel Kgaa Bleach and disinfectant
DE10006997C2 (en) 2000-02-16 2002-11-07 Federal Mogul Friedberg Gmbh Drive seal

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE528604A (en) * 1953-05-06
GB1475064A (en) * 1973-04-18 1977-06-01 Chem Y Fabriek Van Chem Produk Detergent compositions
GB2076010B (en) * 1980-05-13 1984-05-16 Sandoz Products Ltd Bleach composition
NL8103829A (en) * 1981-08-15 1983-03-01 Chem Y AQUEOUS BLEACH WITH CLEANING EFFECT.

Also Published As

Publication number Publication date
DK160103C (en) 1991-06-10
DE3479037D1 (en) 1989-08-24
NL8301168A (en) 1984-10-16
EP0121286A3 (en) 1986-01-22
EP0121286A2 (en) 1984-10-10
DK172184A (en) 1984-10-01
CA1222427A (en) 1987-06-02
EP0121286B1 (en) 1989-07-19
DK172184D0 (en) 1984-03-29

Similar Documents

Publication Publication Date Title
TWI233951B (en) Stabilized bromine solutions, method of manufacture and uses thereof for biofouling control
US3725473A (en) N-(2-hydroxyhydrocarbonyl) iminodicarboxylates
US5679633A (en) Low foam branched alkyldimethylamine oxides
JPH0832914B2 (en) Detergent composition containing ethylenediamine-N, N&#39;-disuccinic acid
JPH05186416A (en) Decomposable chelating agent
JP2007530499A5 (en)
US5972868A (en) Method for controlling alkaline earth and transition metal scaling with 2-hydroxyethyl iminodiacetic acid
DE2614148A1 (en) OXIDIZING AGENTS, BLEACHING AGENTS AND DETERGENTS WITH A BLEACH ACTIVATOR CONTENT
DK160103B (en) CLEANER BASED ON ACTIVE CHLOR AND ALKALI
JPH02295954A (en) 2-methyl- or 2-hydroxymethyl-serine-n, n-diacetic acid and preparation thereof
DK162175B (en) bLEACH FUNDS
JP5567330B2 (en) Composition with unexpected cleaning performance comprising a biodegradable chelating agent
US4029607A (en) Drain cleaning compositions
US3728266A (en) Liquid detergent composition
JPH04323298A (en) Additive for industrial detergent and industrial detergent composition containing the same additive
DE69616085T2 (en) AMINONITRILE INTERMEDIATE PRODUCTS FOR THE PRODUCTION OF 2-HYDROXYETHYLIMINODIACETIC ACID
EP4165153A1 (en) Cleaning product and related synthesis process
US5047577A (en) Quaternary ammonium compounds
EP2987847A1 (en) Use of oxidized humic acid its salts and derivatives in laundry compositions
JP3727083B2 (en) Detergent composition
RU2798937C1 (en) Composition of synthetic detergent with antibacterial effect
RU2226211C2 (en) Detergent liquid agent for treatment of food equipment
JPS608279B2 (en) liquid cleaning composition
US5488130A (en) Amino nitrile intermediate for the preparation of 2-hydroxypropyl iminodiacetic acid
JPH02182798A (en) Liquid detergent composition containing ampholytic surface active agent

Legal Events

Date Code Title Description
PBP Patent lapsed
B1 Patent granted (law 1993)
PBP Patent lapsed