CA1095367A - Liquid detergent-bleach concentrates having high alkalinity - Google Patents
Liquid detergent-bleach concentrates having high alkalinityInfo
- Publication number
- CA1095367A CA1095367A CA307,759A CA307759A CA1095367A CA 1095367 A CA1095367 A CA 1095367A CA 307759 A CA307759 A CA 307759A CA 1095367 A CA1095367 A CA 1095367A
- Authority
- CA
- Canada
- Prior art keywords
- weight
- alkali metal
- hypochlorite
- composition
- diphenyl oxide
- 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.)
- Expired
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 8
- 239000012141 concentrate Substances 0.000 title abstract description 21
- 239000007844 bleaching agent Substances 0.000 title abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 48
- 238000004140 cleaning Methods 0.000 claims abstract description 31
- -1 alkali metal hypochlorite Chemical class 0.000 claims abstract description 29
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 25
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Inorganic materials Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000002689 soil Substances 0.000 claims abstract description 14
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000243 solution Substances 0.000 claims abstract description 12
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims abstract description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims abstract description 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 238000004061 bleaching Methods 0.000 claims description 5
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 4
- SATVIFGJTRRDQU-UHFFFAOYSA-N potassium hypochlorite Chemical compound [K+].Cl[O-] SATVIFGJTRRDQU-UHFFFAOYSA-N 0.000 claims description 4
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 4
- 239000004111 Potassium silicate Substances 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 3
- 235000019353 potassium silicate Nutrition 0.000 claims description 3
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 2
- 235000013311 vegetables Nutrition 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 239000002184 metal Substances 0.000 abstract description 6
- 239000002738 chelating agent Substances 0.000 abstract description 5
- 238000010790 dilution Methods 0.000 abstract description 5
- 239000012895 dilution Substances 0.000 abstract description 5
- 230000007774 longterm Effects 0.000 abstract description 3
- 239000010775 animal oil Substances 0.000 abstract 1
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- 235000008504 concentrate Nutrition 0.000 description 16
- 239000003599 detergent Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000014666 liquid concentrate Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- RVHSTXJKKZWWDQ-UHFFFAOYSA-N 1,1,1,2-tetrabromoethane Chemical compound BrCC(Br)(Br)Br RVHSTXJKKZWWDQ-UHFFFAOYSA-N 0.000 description 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Abstract
LIQUID DETERGENT-BLEACH
CONCENTRATES HAVING HIGH ALKALINITY
Abstract of the Disclosure There are disclosed liquid detergent-bleach concentrates of high alkalinity which are clear solutions having excellent long term stability at elevated temper-atures and at low temperatures. The concentrate compo-sitions consist essentially of an alkali metal hypochlorite, alkali metal chloride, an alkali metal salt of an alkylated diphenyl oxide sulfonic acid, and metal chelating agents in an aqueous composition having a high proportion of alkali metal hydroxide. The concentrates are useful upon dilution in forming hard surface cleaning compositions which are particularly useful in removal of oily soils, derived from animal and vegetable oils.
CONCENTRATES HAVING HIGH ALKALINITY
Abstract of the Disclosure There are disclosed liquid detergent-bleach concentrates of high alkalinity which are clear solutions having excellent long term stability at elevated temper-atures and at low temperatures. The concentrate compo-sitions consist essentially of an alkali metal hypochlorite, alkali metal chloride, an alkali metal salt of an alkylated diphenyl oxide sulfonic acid, and metal chelating agents in an aqueous composition having a high proportion of alkali metal hydroxide. The concentrates are useful upon dilution in forming hard surface cleaning compositions which are particularly useful in removal of oily soils, derived from animal and vegetable oils.
Description
3~S~
BACKGROUND OF THE INVENTION
1. Field of the Invention This invention relates to an aqueous cleaning and bleaching composition containing a stable, concentrated alkali metal hypochlorite composition.
BACKGROUND OF THE INVENTION
1. Field of the Invention This invention relates to an aqueous cleaning and bleaching composition containing a stable, concentrated alkali metal hypochlorite composition.
2 Description_o~ the Prior Art It is known from U. S. Patent 3,172,861 to combine a liquid alkali metal hypochlorite bleaching composition with a bleach-stable deter~ent which can be an alkylated diphenyl oxide sulfonic acid alkali metal salt and to obtain clear compositions which are storage stable at room temperature and free of precipitate or cloudiness after 6 weeks to 4 months shelf-storage at room temperature. In the compositions disclosed therein it has been believed necessary to maintain the con-centrations of ingredients proportionately low in order that the recognized tendency of organic materials to decompose in the presence of oxidizing agents will be minimized. In view of the disclosure contained in this reference therefor, it is unexpected that the applicants have discovered that hypochlorite concentrates containing an alklai metal hydroxide and an alkali metal chloride in addition to an alkali metal hypochlorite and an alkali metal salt of an alkylated diphenyl oxide sulfonic acid can be prepared ~-which are clear, stable to storage at room temperature and at elevated temperatures and at low temperatures and upon dilution are more effective in oily soil removal than the compositions of the prior art.
While stable mixtures of sodium or calcium hypochlorite and a detergent together with compound such as alkali metal phosphates, silicates, carbonates or sulates have been prepared in the dry state and utilized as cleaning compositions upon admixture with water, these dry compositions are intended to be mixed with water immediately prior to use and are neither -2~
- . : ; . , .
.
~9S3~
stable in contact with water nor do they generally form clear aqueous solutions. Thus there is an unfulfilled need for an aqueous liquid concentrate containing an alkali metal hypo-chlorite, alkali and a detergent together with metal chelating agents and metal passivating agents which can be diluted with ,: .
water prior to use to form a stable balanced detergent composition suitable for general purpose or hard surface cleaning. Unex-pectedly, in the liquid concentrates of the invention, the presence of an equimolar amount of alkali metal chloride, based upon the alkali metal hypochlorite, does not adversely affect long-term storage stability or inhibit cleaning efficiency.
Other liquid detergent-bleach compositions are disclosed in U. S. Patent 3,758,409, U. S. Patent 3,929,661 and U. ~O Patent 3t560,389. GeneralIy, such compositions contain ; structurally dissimilar detergents as compared to the detergent used in the compositions of the invention.
SUMMARY OF THE INVENTION
There are disclosed clear, stable at room temperature, at elevated temperatures and at low temperatures alkali metal hypochlorite-detergent concentrates which are useful, upon ~ :1 dilution with water, for general purpose, hard surface cleaning at temperat~res of about 15 C to about 8~ C, and which are particularly useful in removing anlmal and vegetable based oily and fatty soil deposits normally encountered on processing ` equipment in the meat and poultry industry.
D SCR I PT I ON OF THE PREFERl~ED_ EMBOD IMENTS
The concentrates of the invention contain high con-centrations of alkali metal hydroxide and alkali metal chloride said alkali metal chloride preferably present in an equimolar amount based upon the concentration oE alkali metal hypochlorite/
and can contain conventional metal chelating agents and synergists to increase cleaning efficiency. The detergent of the invention , ~
_3--~' 9536;7 which is stable to oxidation in the presence oE an alkali metal hypochlorite consists of an alkylated diphenyl oxide sulfonic acid alkali metal salt. The clear, long-term stable cleaning concentrate composition9 of the invention are high in alkalinity and generally contain, on a weight basis, about 5 to about 20% alkali metal hydroxide, preferably about 8 to about 15% alkali metal hydroxide and most preferably about 10 to about 13~. Generally, ~he concentrates contain, on a weight basis, about 2 to 1S% of an alkali metal hypochlorite, prefer-ably about 2 to about 10~ and most preferably about 2 to about4% and about 0.1 mole to about 1.5 moles of an alkali metal chloride per mole of ~aid hypochlorite. The proportion of the alkali metal salt of an alkylated diphenyl oxide sulfonic acid is generally about 15 to 200% by weight based upon the weight of an alkali metal hypochlorite, preferably about 60 to ~ `
about 200% by weight and most pre~erably about 100 to about 200 by weight. It i~ also desirable to include as part of the composition minor amounts such as about 2% to about 8% each of certain conventional metal passivating or chelating agents such as phosphoric acid, potassium silicate and sodium tripoly-phosphate for their known conventional effects as heavy metal chelating agents and for their known synergistic action in combination with alkali and a detergent in improving cleaning efficiency. Representative alkali metals are sodium, potassium and lithium. The concentrates are dlluted with water for use at the point of use. Generally, active solution concentrations on a weight basis of about 0.5% to about 5% are used for cleaning hard surfaces at application temperatures of about 15 C to ~;
about 80 C and higher~ Preferably about 1% to about 3~ active total weight of the concentrate solution concentrations are used and most preferably about 1% to about 2~ active solution con-centrations are used. Cleaning is accomplished by applicationr ~4~
", ,, ,~
~`
~S3~
of the diluted concentrate of the invention to a hard surface to be cleaned followed by rinsing with water. Optionally, frictional force can be applied to loosen heavy layers of soil.
The alkali metal salts o alkylated diphenyl oxide sulfonic acids are known materials and methods for the pre--paration thereo are disclosed in U. S. Patent 2,854,477 which is incorporated herein by reference. Generally, in the pre-paration of these detergents, alkyl diphenyl ethers are employed as starting materials. These are prepared by methods known in the art such as by reaction of an unsaturated aliphatic hydrocarbon or saturated aliphatic monohalohydrocarbon with a diphenyl ether in the presence of a Friedel-Crafts catalyst.
The sulfonating agent can be chlorosulfonic acid or sulfur trioxide and can be used in amounts of 2 to 2.3 moles per mole of the alkyl diphenyl ether. The sulfonated alkyl diphenyl i ether is converted to the sulfonic acid salt of an alkali metal such as sodium or potassium in order to confer water solubility upon the molecule. Generally, the alkyl moiety of said alkylated diphenyl oxide sulfonic acid alkali metal salt has about 8 to about 22 carbon atoms and the sulfonate groups per diphenyl oxide group average about 1.8 to about 2.3.
In order to determine the relative cleaning efficiency .. --of the concentrates of the invention upon dilution with water, the concentrate of the invention illustrated by Example 1 below was diluted to a solids concentration of 1~ by adding water to the concentrate. For comparison purposes, as shown in Control Example 3, a 1~ by weight solution was made, utilizing a concentrate containing 3% by weight sodium hypochlorite and 8% by welght o~ the sodium salt of sulfonated alkyl diphenyl oxide sold under th~ trademark "DOWFAX 3B-2" by the Dow Chemical Company, Midland, Michigan. In addition, an aqueous concentrate ~ontaining 3% by weight sodium hypochlorite was diluted to 1%
5- ' ` ~G195367 and used as a control as shown in Example 4.
Cleaning efficiency was evaluated, using the method of evaporative rate analysis which has hitherto been applied mainly to analysis oE the surface characteristics of metals ; i as disclosed by Anderson in the November 1969 issue of the ,.~ .
Journal of Colloid and Interface Science. In applying this test method to evaluate the effectiveness with which soil can be removed from a substrate, the difference in radioactivity i~ measured be~ore and aEter cleaning of a soiled surface to which a test solution consisting of a radioactively tagged matQrial in a volatile solvent has been applied. Evaluation is made subsequent to a period of time (i.e., about 3 to 5 , seconds) during which the solvent, after having been applied to the soiled surface, is observed as having evaporated from the surface. For the purposes of the test method utilized herein, a radioactively ta~ged volatile solvent was utilized.
By the method of evaporative rate analysis utilizing a surface analyzer, sold under the registered trademark "Meseran" by . :
ERA Systems, Inc., the non-volatile residue of the test solvent was determined subsequent to the application of a controlled amount of said solvent to the soiled surface to be evaluated.
Approximately 20 microliters of`test solvent is applied to the .
surface to be tested. Subsequent to the deposition on the surface to be tested of this amount of radioactively tagged volatile solvent, the solvent is allowed to interact with the surface bymechanisms such as adsorptiont pexmeation, diffusion, solvation or absorption. It is believed that the rate o~
in~eraction is proportional to the amount of soil on the surface.
¦ 30 For the purposes of evaluation of soil retention in order to determine relative effectiveness of the cleaning composition of the invention, as compared to prior art cleaning . . .
3t53~
compositions, a stainless steel rectangular panel, measuring five inches by two inches was soiled by coating with a solution of O.S~i chicken fat in petroleum ether. The soil was applied to the panel, using a 0.05 milliliter micropipet and the droplet applied thereby was applied by spreading over the panel surface, using a glass microscope slide. After drying, the samples are ready for use in evaluating the cleaning efficiency of the compositions of the invention. It should be noted that prior to the coating o, the stainless steel panels with the chicken fat petroleum ether composition, the panels were first cleaned using a commercial detergent, followed by immersion in boiling trichloroethylene for a period of 30 minutes. In order to determine cleanliness of the panels prior to coating with soil~ the panels were evaluated, using the evaporative rate analysis method utilizing the Meseran~ surface analyzer referred to above. By this method, a radioactively tagged solvent, believed to be a mixture of radioactively tagged lrl,2,2~tetra-bromoethane, 1,1,2-trifluorotrichloroethane and chloroform, was applied to three locations on the panel spaced approximately e~ual distance from each other and positioned along the length-wise dimension of the panel. Cleaned panels show essentially no radioactivity upon evaluation. `~
... ., . ~
In order to evaluate the cleaning efficiency of the compositions of the invention, the soiled panels, having a chi~ken fat coating applied as described above, were immersed in a 1% by weight aqueous solution of the detergent-bleach composition of the invention at a temperature of 150 F. for a period of S minutes. Comparison of the radioactivity retention prior to cleaning and subsequent to cleaning under said con-ditions, provides a measure of the efficiency o the cleaningsolution. The cleaning composition of Example 2 was evaluated against the cleaning compositions of Examples 3 ancl 4 and the . .
ss3~
results are reported in the Eollowing table. In each case, panels were analyzed for retention of radioactivity prior to cleaning and subsequent to cleaning and the difference deter-mined. Results are reported in the table as percent retention of soil, the cleaning composition showing the lowest percent re~ention oE soil being the most efficient cleaning composition.
Table CLEANING EFFICIENCY BY
EVAPORATIVE RATE ANALYSIS
% Soil Retention After Cleaning at 150F, 5 Min., 1~ Solution Exa~ple Test Test Test No. ~lo. 1 No. 2No. 3 2 55 50.~ 61 ~ ,
While stable mixtures of sodium or calcium hypochlorite and a detergent together with compound such as alkali metal phosphates, silicates, carbonates or sulates have been prepared in the dry state and utilized as cleaning compositions upon admixture with water, these dry compositions are intended to be mixed with water immediately prior to use and are neither -2~
- . : ; . , .
.
~9S3~
stable in contact with water nor do they generally form clear aqueous solutions. Thus there is an unfulfilled need for an aqueous liquid concentrate containing an alkali metal hypo-chlorite, alkali and a detergent together with metal chelating agents and metal passivating agents which can be diluted with ,: .
water prior to use to form a stable balanced detergent composition suitable for general purpose or hard surface cleaning. Unex-pectedly, in the liquid concentrates of the invention, the presence of an equimolar amount of alkali metal chloride, based upon the alkali metal hypochlorite, does not adversely affect long-term storage stability or inhibit cleaning efficiency.
Other liquid detergent-bleach compositions are disclosed in U. S. Patent 3,758,409, U. S. Patent 3,929,661 and U. ~O Patent 3t560,389. GeneralIy, such compositions contain ; structurally dissimilar detergents as compared to the detergent used in the compositions of the invention.
SUMMARY OF THE INVENTION
There are disclosed clear, stable at room temperature, at elevated temperatures and at low temperatures alkali metal hypochlorite-detergent concentrates which are useful, upon ~ :1 dilution with water, for general purpose, hard surface cleaning at temperat~res of about 15 C to about 8~ C, and which are particularly useful in removing anlmal and vegetable based oily and fatty soil deposits normally encountered on processing ` equipment in the meat and poultry industry.
D SCR I PT I ON OF THE PREFERl~ED_ EMBOD IMENTS
The concentrates of the invention contain high con-centrations of alkali metal hydroxide and alkali metal chloride said alkali metal chloride preferably present in an equimolar amount based upon the concentration oE alkali metal hypochlorite/
and can contain conventional metal chelating agents and synergists to increase cleaning efficiency. The detergent of the invention , ~
_3--~' 9536;7 which is stable to oxidation in the presence oE an alkali metal hypochlorite consists of an alkylated diphenyl oxide sulfonic acid alkali metal salt. The clear, long-term stable cleaning concentrate composition9 of the invention are high in alkalinity and generally contain, on a weight basis, about 5 to about 20% alkali metal hydroxide, preferably about 8 to about 15% alkali metal hydroxide and most preferably about 10 to about 13~. Generally, ~he concentrates contain, on a weight basis, about 2 to 1S% of an alkali metal hypochlorite, prefer-ably about 2 to about 10~ and most preferably about 2 to about4% and about 0.1 mole to about 1.5 moles of an alkali metal chloride per mole of ~aid hypochlorite. The proportion of the alkali metal salt of an alkylated diphenyl oxide sulfonic acid is generally about 15 to 200% by weight based upon the weight of an alkali metal hypochlorite, preferably about 60 to ~ `
about 200% by weight and most pre~erably about 100 to about 200 by weight. It i~ also desirable to include as part of the composition minor amounts such as about 2% to about 8% each of certain conventional metal passivating or chelating agents such as phosphoric acid, potassium silicate and sodium tripoly-phosphate for their known conventional effects as heavy metal chelating agents and for their known synergistic action in combination with alkali and a detergent in improving cleaning efficiency. Representative alkali metals are sodium, potassium and lithium. The concentrates are dlluted with water for use at the point of use. Generally, active solution concentrations on a weight basis of about 0.5% to about 5% are used for cleaning hard surfaces at application temperatures of about 15 C to ~;
about 80 C and higher~ Preferably about 1% to about 3~ active total weight of the concentrate solution concentrations are used and most preferably about 1% to about 2~ active solution con-centrations are used. Cleaning is accomplished by applicationr ~4~
", ,, ,~
~`
~S3~
of the diluted concentrate of the invention to a hard surface to be cleaned followed by rinsing with water. Optionally, frictional force can be applied to loosen heavy layers of soil.
The alkali metal salts o alkylated diphenyl oxide sulfonic acids are known materials and methods for the pre--paration thereo are disclosed in U. S. Patent 2,854,477 which is incorporated herein by reference. Generally, in the pre-paration of these detergents, alkyl diphenyl ethers are employed as starting materials. These are prepared by methods known in the art such as by reaction of an unsaturated aliphatic hydrocarbon or saturated aliphatic monohalohydrocarbon with a diphenyl ether in the presence of a Friedel-Crafts catalyst.
The sulfonating agent can be chlorosulfonic acid or sulfur trioxide and can be used in amounts of 2 to 2.3 moles per mole of the alkyl diphenyl ether. The sulfonated alkyl diphenyl i ether is converted to the sulfonic acid salt of an alkali metal such as sodium or potassium in order to confer water solubility upon the molecule. Generally, the alkyl moiety of said alkylated diphenyl oxide sulfonic acid alkali metal salt has about 8 to about 22 carbon atoms and the sulfonate groups per diphenyl oxide group average about 1.8 to about 2.3.
In order to determine the relative cleaning efficiency .. --of the concentrates of the invention upon dilution with water, the concentrate of the invention illustrated by Example 1 below was diluted to a solids concentration of 1~ by adding water to the concentrate. For comparison purposes, as shown in Control Example 3, a 1~ by weight solution was made, utilizing a concentrate containing 3% by weight sodium hypochlorite and 8% by welght o~ the sodium salt of sulfonated alkyl diphenyl oxide sold under th~ trademark "DOWFAX 3B-2" by the Dow Chemical Company, Midland, Michigan. In addition, an aqueous concentrate ~ontaining 3% by weight sodium hypochlorite was diluted to 1%
5- ' ` ~G195367 and used as a control as shown in Example 4.
Cleaning efficiency was evaluated, using the method of evaporative rate analysis which has hitherto been applied mainly to analysis oE the surface characteristics of metals ; i as disclosed by Anderson in the November 1969 issue of the ,.~ .
Journal of Colloid and Interface Science. In applying this test method to evaluate the effectiveness with which soil can be removed from a substrate, the difference in radioactivity i~ measured be~ore and aEter cleaning of a soiled surface to which a test solution consisting of a radioactively tagged matQrial in a volatile solvent has been applied. Evaluation is made subsequent to a period of time (i.e., about 3 to 5 , seconds) during which the solvent, after having been applied to the soiled surface, is observed as having evaporated from the surface. For the purposes of the test method utilized herein, a radioactively ta~ged volatile solvent was utilized.
By the method of evaporative rate analysis utilizing a surface analyzer, sold under the registered trademark "Meseran" by . :
ERA Systems, Inc., the non-volatile residue of the test solvent was determined subsequent to the application of a controlled amount of said solvent to the soiled surface to be evaluated.
Approximately 20 microliters of`test solvent is applied to the .
surface to be tested. Subsequent to the deposition on the surface to be tested of this amount of radioactively tagged volatile solvent, the solvent is allowed to interact with the surface bymechanisms such as adsorptiont pexmeation, diffusion, solvation or absorption. It is believed that the rate o~
in~eraction is proportional to the amount of soil on the surface.
¦ 30 For the purposes of evaluation of soil retention in order to determine relative effectiveness of the cleaning composition of the invention, as compared to prior art cleaning . . .
3t53~
compositions, a stainless steel rectangular panel, measuring five inches by two inches was soiled by coating with a solution of O.S~i chicken fat in petroleum ether. The soil was applied to the panel, using a 0.05 milliliter micropipet and the droplet applied thereby was applied by spreading over the panel surface, using a glass microscope slide. After drying, the samples are ready for use in evaluating the cleaning efficiency of the compositions of the invention. It should be noted that prior to the coating o, the stainless steel panels with the chicken fat petroleum ether composition, the panels were first cleaned using a commercial detergent, followed by immersion in boiling trichloroethylene for a period of 30 minutes. In order to determine cleanliness of the panels prior to coating with soil~ the panels were evaluated, using the evaporative rate analysis method utilizing the Meseran~ surface analyzer referred to above. By this method, a radioactively tagged solvent, believed to be a mixture of radioactively tagged lrl,2,2~tetra-bromoethane, 1,1,2-trifluorotrichloroethane and chloroform, was applied to three locations on the panel spaced approximately e~ual distance from each other and positioned along the length-wise dimension of the panel. Cleaned panels show essentially no radioactivity upon evaluation. `~
... ., . ~
In order to evaluate the cleaning efficiency of the compositions of the invention, the soiled panels, having a chi~ken fat coating applied as described above, were immersed in a 1% by weight aqueous solution of the detergent-bleach composition of the invention at a temperature of 150 F. for a period of S minutes. Comparison of the radioactivity retention prior to cleaning and subsequent to cleaning under said con-ditions, provides a measure of the efficiency o the cleaningsolution. The cleaning composition of Example 2 was evaluated against the cleaning compositions of Examples 3 ancl 4 and the . .
ss3~
results are reported in the Eollowing table. In each case, panels were analyzed for retention of radioactivity prior to cleaning and subsequent to cleaning and the difference deter-mined. Results are reported in the table as percent retention of soil, the cleaning composition showing the lowest percent re~ention oE soil being the most efficient cleaning composition.
Table CLEANING EFFICIENCY BY
EVAPORATIVE RATE ANALYSIS
% Soil Retention After Cleaning at 150F, 5 Min., 1~ Solution Exa~ple Test Test Test No. ~lo. 1 No. 2No. 3 2 55 50.~ 61 ~ ,
3 Control 74 86 69
4 Control 80 96 97 The following examples illustrate the various aspects of the invention including methods of preparing the compositions of the invention but are not intended to limit its scope. Where not otherwise speciEied throughout this specification and claims, temperatures are qiven in degrees Centigrade and parts, per-centages and proportions are by weight.
A foaming, chlorinated liquid alkaline detergent concentrate useful in the preparation of aqueous qleaning compositions which are effective in removing fatty and oily soils from food processing equipment was prepared by combining the following ingredients. To a kettle there was added 51,5 parts by weight of water, 26 parts by weight of a 45% by weight solution o~ potassium hydroxide. The water and potassium hydroxide solution was thoroughly mixed and then there was added . . .
g5367 phosphoric acid 3.5 parts by weight; potassium silicate, 2 parts by weight; and sodium tripolyphosphate, 6 parts by weight.
After thoroughly dissolving these ingredients, 3 parts by weight of liquid chlorine was added to the mixture while under rapid agitation. By reaction of this chlorine with an equal molar amount ofa portion of the potassium hydroxide present, equimolar amounts of potassium hypochlorite and potassium chloride are generated in situ in accordance with the following equation:
C12 + KOH ~ KOCl ~ KCl Upon attaining homogeneity of the mixture, there was added 4 parts by weight of the sodium salt of a sulfonated alkyl diphenyl oxide sold under the trademarlc "DOWFAX 3~-2" by the Dow Chemical Company, Midland, Michigan. It is understood that this material is sodium dodecyl diphenyl oxide disulfonate.
This liquid composition formed a stable solution which was clear at room temperature, at I20 C and at 0 F, which is the approximate freezing point of said solution. Such com-positions show excellent storage stability and substantially unchanged clarity as well as freedom from separation and precipitation of ingredients when stored over an extended period of two months at a temperature of 120 F or at a temper-...... :
ature of 0 F as well as at room temperature. The alkali metalhypochlorite bleaching activity is retained in such concentrate3 upon extended storage, as noted above, so that upon dilution at the time of use substantially the same bleaching effect is obtained in comparison with freshly prepared and diluted concentrates.
The concentrate of Example 1 was diluted with water to a concentration of 1% by weight.
EXAMPLE_3 (Control) A bleach-detergent composition of the prior art _g_ ~ 536~
was prepared consisting of 3~ by weight sodium hypochlorite, 8% by weight of the sodium salt of a sulfonated alkyl diphenyl oxide under the trademark "DOWFAX 3B-2" and water to 100%.
The composition was diluted to a concentration of 1% by weight , ~or use.
EXAMPLE 4 (Control) A 3% by weight aqueous solution of sodiu~ hypochlorite was prepared and further diluted with water to a concentration of 1% by weight for use.
;~
: ' ' :.
,, --1 0-- `
A foaming, chlorinated liquid alkaline detergent concentrate useful in the preparation of aqueous qleaning compositions which are effective in removing fatty and oily soils from food processing equipment was prepared by combining the following ingredients. To a kettle there was added 51,5 parts by weight of water, 26 parts by weight of a 45% by weight solution o~ potassium hydroxide. The water and potassium hydroxide solution was thoroughly mixed and then there was added . . .
g5367 phosphoric acid 3.5 parts by weight; potassium silicate, 2 parts by weight; and sodium tripolyphosphate, 6 parts by weight.
After thoroughly dissolving these ingredients, 3 parts by weight of liquid chlorine was added to the mixture while under rapid agitation. By reaction of this chlorine with an equal molar amount ofa portion of the potassium hydroxide present, equimolar amounts of potassium hypochlorite and potassium chloride are generated in situ in accordance with the following equation:
C12 + KOH ~ KOCl ~ KCl Upon attaining homogeneity of the mixture, there was added 4 parts by weight of the sodium salt of a sulfonated alkyl diphenyl oxide sold under the trademarlc "DOWFAX 3~-2" by the Dow Chemical Company, Midland, Michigan. It is understood that this material is sodium dodecyl diphenyl oxide disulfonate.
This liquid composition formed a stable solution which was clear at room temperature, at I20 C and at 0 F, which is the approximate freezing point of said solution. Such com-positions show excellent storage stability and substantially unchanged clarity as well as freedom from separation and precipitation of ingredients when stored over an extended period of two months at a temperature of 120 F or at a temper-...... :
ature of 0 F as well as at room temperature. The alkali metalhypochlorite bleaching activity is retained in such concentrate3 upon extended storage, as noted above, so that upon dilution at the time of use substantially the same bleaching effect is obtained in comparison with freshly prepared and diluted concentrates.
The concentrate of Example 1 was diluted with water to a concentration of 1% by weight.
EXAMPLE_3 (Control) A bleach-detergent composition of the prior art _g_ ~ 536~
was prepared consisting of 3~ by weight sodium hypochlorite, 8% by weight of the sodium salt of a sulfonated alkyl diphenyl oxide under the trademark "DOWFAX 3B-2" and water to 100%.
The composition was diluted to a concentration of 1% by weight , ~or use.
EXAMPLE 4 (Control) A 3% by weight aqueous solution of sodiu~ hypochlorite was prepared and further diluted with water to a concentration of 1% by weight for use.
;~
: ' ' :.
,, --1 0-- `
Claims (8)
1. A cleaning and bleaching liquid composition consisting essentially of an aqueous solution of:
A. about 2% to about 15% by weight of an alkali metal hypochlorite, B. about 15% to about 200% by weight of an alkali metal salt of an alkylated diphenyl oxide sulfonic acid based upon said alkali metal hypochlorite weight, C. about 5% to about 20% by weight of an alkali metal hydroxide, and D. an alkali metal chloride.
A. about 2% to about 15% by weight of an alkali metal hypochlorite, B. about 15% to about 200% by weight of an alkali metal salt of an alkylated diphenyl oxide sulfonic acid based upon said alkali metal hypochlorite weight, C. about 5% to about 20% by weight of an alkali metal hydroxide, and D. an alkali metal chloride.
2. The composition of claim wherein said hypochlorite is selected from the group consisting of sodium hypochlorite and potassium hypochlorite and is present in the proportion of about 3% to about 10% by weight and said alkali metal salt of an alkylated diphenyl oxide sulfonic acid is present in the proportion of about 30% to about 175% by weight on the basis of the weight of said hypochlorite.
3. The composition of claim 2 wherein said alkali metal salt of an alkylated diphenyl oxide sulfonic acid contains about 8 to about 22 carbon atoms in the alkyl moiety and an average of about 1.8 to 2.3 sulfonate groups per diphenyl oxide moiety.
4. The composition of claim 3 wherein said composition consists essentially of about 2% to about 4% by weight of potas-sium hypochlorite, an equimolar amount of potassium chloride and about 100% to about 200% by weight on the basis of the weight of said potassium hypochlorite of said sulfonated alkyl diphenyl oxide.
5. The composition of claim 4 wherein said composition contains on a weight basis about 8% to about 15% of potassium hydroxide, about 2% potassium silicate, about 3.5% phosphoric acid and about 6% sodium tripolyphosphate.
6. A method of cleaning hard surfaces comprising:
A. forming an aqueous solution of about 0.5% to about 5% by weight active solution concentration of the composition of claim 1, B. applying an effective amount of said mixture to said hard surface, and C. rinsing said surface with water.
A. forming an aqueous solution of about 0.5% to about 5% by weight active solution concentration of the composition of claim 1, B. applying an effective amount of said mixture to said hard surface, and C. rinsing said surface with water.
7. The method of claim 6 wherein said mixture is applied at a temperature of about 15° C to about 80° C to hard surfaces soiled with animal and vegetable-based oily soils.
8. A method of cleaning hard surfaces comprising:
A. forming an aqueous solution of 0.5% to about 5%
by weight active solution concentration of the composition of claim 5, B. applying an effective amount of said mixture to said hard surface, and C. rinsing said surface with water.
A. forming an aqueous solution of 0.5% to about 5%
by weight active solution concentration of the composition of claim 5, B. applying an effective amount of said mixture to said hard surface, and C. rinsing said surface with water.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81926177A | 1977-07-27 | 1977-07-27 | |
US819,261 | 1977-07-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1095367A true CA1095367A (en) | 1981-02-10 |
Family
ID=25227641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA307,759A Expired CA1095367A (en) | 1977-07-27 | 1978-07-20 | Liquid detergent-bleach concentrates having high alkalinity |
Country Status (4)
Country | Link |
---|---|
AU (1) | AU521730B2 (en) |
BR (1) | BR7804821A (en) |
CA (1) | CA1095367A (en) |
ZA (1) | ZA784238B (en) |
-
1978
- 1978-07-20 CA CA307,759A patent/CA1095367A/en not_active Expired
- 1978-07-26 ZA ZA00784238A patent/ZA784238B/en unknown
- 1978-07-26 AU AU38359/78A patent/AU521730B2/en not_active Expired
- 1978-07-26 BR BR7804821A patent/BR7804821A/en unknown
Also Published As
Publication number | Publication date |
---|---|
AU3835978A (en) | 1980-01-31 |
AU521730B2 (en) | 1982-04-29 |
ZA784238B (en) | 1979-08-29 |
BR7804821A (en) | 1979-04-10 |
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