US2240957A - Process for avoiding and rendering harmless the precipitates of water insoluble metal salts - Google Patents
Process for avoiding and rendering harmless the precipitates of water insoluble metal salts Download PDFInfo
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- US2240957A US2240957A US107020A US10702036A US2240957A US 2240957 A US2240957 A US 2240957A US 107020 A US107020 A US 107020A US 10702036 A US10702036 A US 10702036A US 2240957 A US2240957 A US 2240957A
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- 150000003839 salts Chemical class 0.000 title description 27
- 239000002244 precipitate Substances 0.000 title description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 19
- 238000000034 method Methods 0.000 title description 15
- 229910052751 metal Inorganic materials 0.000 title description 8
- 239000002184 metal Substances 0.000 title description 8
- 238000009877 rendering Methods 0.000 title description 6
- 239000008233 hard water Substances 0.000 description 19
- 239000002253 acid Substances 0.000 description 17
- -1 aliphatic alcohols Chemical class 0.000 description 15
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 12
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
- 239000000344 soap Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 238000005406 washing Methods 0.000 description 12
- 159000000000 sodium salts Chemical class 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 7
- 239000000292 calcium oxide Substances 0.000 description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 159000000007 calcium salts Chemical class 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- XWSGEVNYFYKXCP-UHFFFAOYSA-N 2-[carboxymethyl(methyl)amino]acetic acid Chemical compound OC(=O)CN(C)CC(O)=O XWSGEVNYFYKXCP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000008234 soft water Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Chemical compound OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- PQHYOGIRXOKOEJ-UHFFFAOYSA-N 2-(1,2-dicarboxyethylamino)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)NC(C(O)=O)CC(O)=O PQHYOGIRXOKOEJ-UHFFFAOYSA-N 0.000 description 1
- KEZYHIPQRGTUDU-UHFFFAOYSA-N 2-[dithiocarboxy(methyl)amino]acetic acid Chemical compound SC(=S)N(C)CC(O)=O KEZYHIPQRGTUDU-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical class OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 101000907988 Petunia hybrida Chalcone-flavanone isomerase C Proteins 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
- 229910001626 barium chloride Inorganic materials 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229940003871 calcium ion Drugs 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- MRQIXHXHHPWVIL-UHFFFAOYSA-N chembl1397023 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=CC=C1 MRQIXHXHHPWVIL-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 210000004081 cilia Anatomy 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 235000019239 indanthrene blue RS Nutrition 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000005494 tarnishing Methods 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/325—Amines
- D06M13/342—Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines
Definitions
- My present invention relates to a process for avoiding and rendering harmless precipitates of water insoluble metal salts more particularly the precipitates formed owing to the hardness of water.
- a large number of various protective colloids are already known which are capable of avoiding in soaping processes the precipitation of calcium salts of hard water in a coarse form or of dispersing the precipitates formed. They are useful for avoiding chalky stains on textile goods but they are unable to avoid loss of soap in hard water since the dispersed chalky soap does not foam and has no detergent power, nor can they prevent the precipitation of calcium carbonate occurring particularly at higher temperatures and in the presence of alkalies, which precipitates may likewise be deposited on the textile goods. In many cases other is which tend to form scarcely glllhlcmninsoluble precipitates may have a distyLbinaaefiect. Thus water containing iron effects, as itis well known, a strong turning of the goods to yellow and injures the shade of some dyestuffs. When textile goods are washed in zinc lined vessels even precipitates of zinc soaps may be formed on the goods.
- aluminium soaps are used for waterproofing goods. If it is required to render such goods wettable again it is often necessary to remove the aluminium salts from the fiber.
- aminocarboxylic acids of the aforesaid type which are useful for the present process of which only some examples can be named.
- aminocarboxylic acids of the aforesaid type which are useful for the present process of which only some examples can be named.
- CIlaCOOH cmcoon coon (Beilstein, fourth edition, vol. 14, page 354) is alkyior arylgroups suitable compounds are obtained, for instance C-phenyl-nitrilotriacetic acid of the formula:
- Such washing and deterging and the like liquors may contain besides the aforesaid aminocarboxyiic acids further ingredients, which due to the presence of the aminocarboxylic acid can exhibit their own effect for instance in hard water in the same manner as when applied in soft water free from metal salts.
- Such an ingredient is particularly soap, but also other deterging agents, 1. e. besides the salts of the'higher fatty acids (the soaps) salts of sulfonic acid deriva- Aminocarboxylic acids which.
- alkylated naphthalene sulfonic acids for instance alkylated naphthalene sulfonic acids, water soluble salts of acid sulfuric acid esters of higher aliphatic alcohols such as of lauryl-, cetylor oleyl-alcohol, salts of condensation products of fatty acids with for instance hydroxyor aminoalkylsulfonic acids and the like.
- Such bodies may be previously mixed with the present aminocarboxylic acid and the mixture may be added to the liquors in question or the single ingredients may be added in any sequence in suitable properties of weight to the aqueous liquors.
- ingredients such as sodium sulfate, sodium carbonate, silicates and phosphates, oxidants or reducing agents such as perborates and hydrosulflte, organic servants an e like.
- Example 1 To hard water containing 0.2 gram of calcium oxide per liter 2 grs. of the sodium salt of trimethylarnino-a-a-u-tricarboxylic acid per liter are added care being taken to establish an alkaline reaction by adding a small quantity of sodium carbonate. On adding thereto while hot 1 to 2 grs. of soap per liter a clear strongly foaming solution of very good detergent power is obtained. Such an aqueous liquor exhibits no precipitate of calcium carbonate even when boiled with the addition of sodium carbonate or caustic soda.
- Example 2 A cotton tissue, which has been repeatedly washed with hard water and is therefore strongly intermingled with precipitates of chalky soap, containing according to analysis 1.5% of calcium oxide and after treatment with hydrochloric acid 10.5% of fat which can be extracted, is treated for about an hour with a boiling liquor which has been made alkaline and contains in the liter of the trimethylamine-a-a-a"-tricarboxylic acid. After washing out and drying the chalky soap has been practically removed from the goods.
- the tissue contains according to analysis 0.05% of calcium oxide and 0.6% of fat.
- Example 3 To a hard water containing 0.1 gram of calcium oxide per liter 1% of its weight of crystallized sodium metasilicate-pentahydrate and 0.05% of its weight of the sodium salt of the trimethylamine-tricarboxylic acid are added. When boiling oil the liquor a clear solution is obtained. whereas without such an addition fiocky precipitates are formed.
- Example 4 To 100 parts of a solution containing parts of an aminocarboxylic acid obtainable by entirely hydrolizing albumen parts of monochloroacetic acid and parts of sodium carbonate are added. By heating the mixture for Examiner 10 to 12 hours at 95 to 100 C. and drying it a brownish powder is obtained which is likewise able of making harmless the hardness of water and of avoiding precipitates of calcium salts.
- Example Cotton yarn is dyed with 3% of its weight of Sirius light green BL (Schultz, Farbstofitabellen, (1934) first volume of addition, page 131) with the addition per liter of grs. of sodium sulfate and 5 grs. of the sodium salt of the methyliminodiacetic acid (Beilstein, fourth edition, vol. IV, page 367) for about an hour at 90 to 95 C. while using a hard water containing 0.12 gram of calcium oxide per liter.
- the goods are dyed in an unobjectionable manner whereas without the addition of the methyliminodiacetic acid the goods are dyed unequally owing to the sensitiveness of the dyestuff towards chalk.
- Example 6 Cotton goods in the form of cops or cross bobbins are dyed on any usual dyeing apparatus with of its weight of a paste of Indanthrene scarlet B (Schultz, Farbstofitabellen, vol. II (1932), page 132) according to a process usual for such a vat dyestuif while using a hard water containing 0.15 gram of calcium oxide per liter, to the dyeing liquor per liter 3 grs. of the sodium salt of the anthranilic-N,N-diacetic acid being added.
- the goods are dyed in an unobjectionable manner whereas without such an addition white dusty precipitates of calcium salt are formed.
- Example 7 When using in Example 1 instead of the sodium salt of the nitrilotriacetic acid mentioned therein the same quantity of the sodium salt of the C-phenyl-nitrilotriacetic acid likewise a clear well foaming solution is obtained.
- the aforesaid acid may be prepared as follows: A mixture of 150 parts of a-aminophenylacetic acid (Beilstein, fourth edition, vol. 14, page 460), 285 parts of monochloroacetic acid, 375 parts of sodium carbonate and 800 parts of water is slowly heated to 95 to 100 C. and after stirring for some hours at this temperature 470 parts of hydrochloric acid of B. are added. After some time the C-pheny1-nitrilo-triacetic acid separates as a white crystalline powder.
- a-aminophenylacetic acid Beilstein, fourth edition, vol. 14, page 460
- monochloroacetic acid 375 parts of sodium carbonate
- 800 parts of water is slowly heated to 95 to 100 C. and after stirring for some hours at this temperature 470 parts of hydrochloric acid of B. are added. After some time the C-pheny1-nitrilo-triacetic acid separates as a white crystalline powder.
- Example 8 According to one of the usual methods 2 grs. of 2.3-hydroxynaphthoic acid-B-naphthalide are dissolved in a caustic soda solution with the addition of hot water while using a hard water containing 0.12 gram of calcium oxide per liter and further on adding per liter 3 grs. of the sodium salt of the iminobissuccinic acid of the formula:
- Example 9 In the same manner as described in the foregoing examples the ethylene-bis-(iminodiacetic) acid of the formula:
- HOOC.H2C CHQ-COOH may be used. It may be prepared either by saponifying the corresponding nitril or by acting with monochloro-acetic acid on ethylene diamine for instance in the following manner: 60 parts of ethylene diamine in an aqueous solution of 10% strength are mixed with 466 parts of the sodium salt of monochloroacetic acid and 212 parts of sodium carbonate and the mixture is heated at to C. for 8 to 10 hours. Then 470 parts of a hydrochloric acid of 20 B. are added. When cool, the aforesaid acid precipitates. It is dimculty soluble in cold water and may be recrystallized from water.
- Example 10 Cotton goods are dyed as described in Example 6, but while adding per liter 2 grs. of the sodium salt of an acid of the formula:
- Example 11 10 parts of the sulfuric acid ester of oleylalcohol (or of another synthetical deterging agent) are mixed with 15 parts of sodium perborate, 20 parts of sodium silicate, 15 parts of the sodium salt of the nitrolotriacetic acid and 40 parts of sodium chloride. In this manner a deterging agent very suitable for boiling washing processes which is clearly soluble even in hard water is obtained.
- centrated solution 10 grs. of sodium sulfate is added. At first the solution remains clear and becomes strongly turbid only after standing for some time. The barium sulfate which precipitates in a very fine state begins to sink down only after some hours.
- Such a solution may be advantageously used for tarnishing artificial silk.
- R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R1 standing for a member of the group consisting of hydrogen and alkyl.
- Cross Reference 4 The process of washing which comprises adding to hard water alkali metal salts of carboxylic acids of the general formula:
- R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R2 standing for a member of the group consisting of hydrogen and alkyl, adding a Water-soluble detergent of the group consisting of salts of sulfonic acid derivatives of aliphatic and aromatic hydrocarbons, salts of acid sulfuric acid esters of higher aliphatic alcohols, salts of -condensation products of fatty acids with hydroxy alkyl sulfonic acids and salts of condensation products of fatty acids with amino alkyl sulfonic acids to the water and washing the materials to be cleansed with the water thus treated.
- R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R2 standing for a member of the group consisting of hydrogen and alkyl, adding a water-soluble soap to the water and washing the materials to be cleansed with the water thus treated.
- washing composition a mixture consisting of a water-soluble soap and an alkali metal salt of a carboxylic acid of the general formula:
- cmcoon x-crncoon Examiner wherein R stands for a member selected the group consisting of the radicles from R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R: standing for a member of the group consisting of hydrogen and alkyl.
- washing composition a mixture consisting of a water-soluble detergent oi the group consisting of salts of suifonic acid derivatives of aliphatic and aromatic hydrocarbons, salts of acid sulfuric acid esters of higher aliphatic alcohols, salts of condensation products of fatty acids with. hydroxy allzyl sulfonic acids and salts of condensation products of fatty acids with amino alliyl SLfl-fOIliC acids and an alkali metal salt of a carboxylic acid of the general formula:
- R stands for a member selected from the group consisting of the radicles cilia ooii R1 ancling for a member of the group consisting of hydrogen, a kyl ncl phony; and R: standing for a member of the group consisting of hydrogen and allz'gl.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
Description
252. UUMlUbl l mo.
Patented May 6, 1941 PROCESS FOR AVOIDING AND RENDERING HARMLESS THE PRECIPITATES OF WATER INSOLUBLE MIETAL SALTS Ferdinand Miinz, Frankfort-on-the-Main, Germany, assignor, by mesne assignments, to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application October 22, 1936, Serial No. 107,020. In Germany October 30, 1935 7 Claims.
My present invention relates to a process for avoiding and rendering harmless precipitates of water insoluble metal salts more particularly the precipitates formed owing to the hardness of water.
A large number of various protective colloids are already known which are capable of avoiding in soaping processes the precipitation of calcium salts of hard water in a coarse form or of dispersing the precipitates formed. They are useful for avoiding chalky stains on textile goods but they are unable to avoid loss of soap in hard water since the dispersed chalky soap does not foam and has no detergent power, nor can they prevent the precipitation of calcium carbonate occurring particularly at higher temperatures and in the presence of alkalies, which precipitates may likewise be deposited on the textile goods. In many cases other is which tend to form scarcely glllhlcmninsoluble precipitates may have a distyLbinaaefiect. Thus water containing iron effects, as itis well known, a strong turning of the goods to yellow and injures the shade of some dyestuffs. When textile goods are washed in zinc lined vessels even precipitates of zinc soaps may be formed on the goods.
Generally aluminium soaps are used for waterproofing goods. If it is required to render such goods wettable again it is often necessary to remove the aluminium salts from the fiber.
According to my present invention there are added to aqueous liquors containing metal salts of the aforesaid type organic aminocarboxylic acids containing in relation to one basic nitrogen atom more than one carboxylic acid group stand- ;ing in a-position thereto. When adding these lsubstances to aqueous liquors in the presence of metal salts which tend to form or have already formed difficultly soluble or insoluble precipitates particularly to hard water such precipittates are made harmless under particularly fa- .vorable conditions.
In all the above cases the addition of the said aminocarboxylic acids which mostly have no colloid character is of great advantage. Hard water which contains such an addition acts as soft water towards agents which precipitate chalk. It may be that the said aminocarboxylic acids bind the calcium-ion in a complex form. In consequence thereof one needs no more soap for washing when using hard water containing such an addition than in the case of distilled water.
The same good result is obtained when adding the aforesaid substances to aqueous liquors apv i t plied for other improving processes for textile goods, such as for dying processes.
Even when using dyestuffs which are not sensitive towards chalk, precipitates of calcium carbonate may occur. Dyestuffs which are sensitive toward chalk form precipitates of insoluble salts. In all these cases the addition of the aforesaid products is of advantage.
Likewise existing precipitates of insoluble calcium or other metal salts can be redissolved without using strong acids which may be detrimental to fabrics and apparatus.
In many cases of particularly insoluble salts, for instance of barium sulfate and calcium oxalate, by adding the aforesaid amino carboxylic acids an entirely clear solution is not obtainable, but the formation of the precipitates only occurs slowly and in a finely dispersed state.
There exists a great number of aminocarboxylic acids of the aforesaid type which are useful for the present process of which only some examples can be named. Among the simplest compounds which are obtainable by acting with ammonia on monochloracetic acid or by saponifying nitrils the trirnethylamine-m,a'.a"- tricarboxylic acid or nitrilotriacetic acid of the formula:
CHLCOOH I NCHa.COOH .902-;
(Beilstein, fourth edition, volume IV, page 369) is particularly suitable. The iminodiacetic acid of the formula:
CH2.COOH
CHi-COOH CHaC O OH Alkyl-N CHI-C O OH Examiner 252. COMFOSiiiONS.
are essentially more effective than the less useful aryliminodiacetic acids of the formula:
CH:.COOH
ArylN CH2.COOH
But if the latter contain in the benzene nucleus an acid group standing in ortho position to the carbon atom to which the iminogroup is attached the efficacy is essentially increased, for instance the anthranilic-NN-diacetic acid of the formula:
CIlaCOOH cmcoon coon (Beilstein, fourth edition, vol. 14, page 354) is alkyior arylgroups suitable compounds are obtained, for instance C-phenyl-nitrilotriacetic acid of the formula:
cm. 0 on C-monomethyl-nitrilotriacetic acid,
" C-dimethyl-nitrilotriacetic acid of the formula:
/CH2.COOH N-CH2COOH C.COOH CH1 CH1 C-cyclohexenyl-nitrilotriacetic acid of the formula:
cincoon These aminocarboxylic acids, which correspond to the aforesaid general formula, have more or less the said effect in an aqueous medium according to their chemical constitution.
As pointed out above one may make use of this effect generally for washing, deterging and other improving processes of textile goods, but likewise for washing or treating otherwise subjects of various use, such as pieces of furniture, floors, windows, animal hairs and the like.
Such washing and deterging and the like liquors may contain besides the aforesaid aminocarboxyiic acids further ingredients, which due to the presence of the aminocarboxylic acid can exhibit their own effect for instance in hard water in the same manner as when applied in soft water free from metal salts. Such an ingredient is particularly soap, but also other deterging agents, 1. e. besides the salts of the'higher fatty acids (the soaps) salts of sulfonic acid deriva- Aminocarboxylic acids which.
. grs.
tives of aliphatic and aromatic hydrocarbons, for instance alkylated naphthalene sulfonic acids, water soluble salts of acid sulfuric acid esters of higher aliphatic alcohols such as of lauryl-, cetylor oleyl-alcohol, salts of condensation products of fatty acids with for instance hydroxyor aminoalkylsulfonic acids and the like.
Such bodies may be previously mixed with the present aminocarboxylic acid and the mixture may be added to the liquors in question or the single ingredients may be added in any sequence in suitable properties of weight to the aqueous liquors.
To such mixtures further ingredients may be added such as sodium sulfate, sodium carbonate, silicates and phosphates, oxidants or reducing agents such as perborates and hydrosulflte, organic servants an e like.
In order to further illustrate my invention the following examples are given, the parts being by weight and all temperatures in centrigrade degrees and the degrees of hardness of the water being German degrees. But I wish it, however, to be understood that my invention is not limited to the examples given, nor to the exact conditions stated therein.
Example 1 To hard water containing 0.2 gram of calcium oxide per liter 2 grs. of the sodium salt of trimethylarnino-a-a-u-tricarboxylic acid per liter are added care being taken to establish an alkaline reaction by adding a small quantity of sodium carbonate. On adding thereto while hot 1 to 2 grs. of soap per liter a clear strongly foaming solution of very good detergent power is obtained. Such an aqueous liquor exhibits no precipitate of calcium carbonate even when boiled with the addition of sodium carbonate or caustic soda.
Instead of the tricarboxylic acid one may use the iminodiacetic acid but with a somewhat reduced effect.
Example 2 A cotton tissue, which has been repeatedly washed with hard water and is therefore strongly intermingled with precipitates of chalky soap, containing according to analysis 1.5% of calcium oxide and after treatment with hydrochloric acid 10.5% of fat which can be extracted, is treated for about an hour with a boiling liquor which has been made alkaline and contains in the liter of the trimethylamine-a-a-a"-tricarboxylic acid. After washing out and drying the chalky soap has been practically removed from the goods. The tissue contains according to analysis 0.05% of calcium oxide and 0.6% of fat.
Example 3 To a hard water containing 0.1 gram of calcium oxide per liter 1% of its weight of crystallized sodium metasilicate-pentahydrate and 0.05% of its weight of the sodium salt of the trimethylamine-tricarboxylic acid are added. When boiling oil the liquor a clear solution is obtained. whereas without such an addition fiocky precipitates are formed.
Example 4 To 100 parts of a solution containing parts of an aminocarboxylic acid obtainable by entirely hydrolizing albumen parts of monochloroacetic acid and parts of sodium carbonate are added. By heating the mixture for Examiner 10 to 12 hours at 95 to 100 C. and drying it a brownish powder is obtained which is likewise able of making harmless the hardness of water and of avoiding precipitates of calcium salts.
Example Cotton yarn is dyed with 3% of its weight of Sirius light green BL (Schultz, Farbstofitabellen, (1934) first volume of addition, page 131) with the addition per liter of grs. of sodium sulfate and 5 grs. of the sodium salt of the methyliminodiacetic acid (Beilstein, fourth edition, vol. IV, page 367) for about an hour at 90 to 95 C. while using a hard water containing 0.12 gram of calcium oxide per liter.
The goods are dyed in an unobjectionable manner whereas without the addition of the methyliminodiacetic acid the goods are dyed unequally owing to the sensitiveness of the dyestuff towards chalk.
Example 6 Cotton goods in the form of cops or cross bobbins are dyed on any usual dyeing apparatus with of its weight of a paste of Indanthrene scarlet B (Schultz, Farbstofitabellen, vol. II (1932), page 132) according to a process usual for such a vat dyestuif while using a hard water containing 0.15 gram of calcium oxide per liter, to the dyeing liquor per liter 3 grs. of the sodium salt of the anthranilic-N,N-diacetic acid being added. The goods are dyed in an unobjectionable manner whereas without such an addition white dusty precipitates of calcium salt are formed.
Example 7 When using in Example 1 instead of the sodium salt of the nitrilotriacetic acid mentioned therein the same quantity of the sodium salt of the C-phenyl-nitrilotriacetic acid likewise a clear well foaming solution is obtained.
The aforesaid acid may be prepared as follows: A mixture of 150 parts of a-aminophenylacetic acid (Beilstein, fourth edition, vol. 14, page 460), 285 parts of monochloroacetic acid, 375 parts of sodium carbonate and 800 parts of water is slowly heated to 95 to 100 C. and after stirring for some hours at this temperature 470 parts of hydrochloric acid of B. are added. After some time the C-pheny1-nitrilo-triacetic acid separates as a white crystalline powder.
The C-dimethyland C-cyclohexenylnitrilotriacetic acid which are obtainable in an analogous manner have a similar efiect.
Example 8 According to one of the usual methods 2 grs. of 2.3-hydroxynaphthoic acid-B-naphthalide are dissolved in a caustic soda solution with the addition of hot water while using a hard water containing 0.12 gram of calcium oxide per liter and further on adding per liter 3 grs. of the sodium salt of the iminobissuccinic acid of the formula:
C13H2.COOH (H.COOH
CELCOOH CH2.COOH
(which salt is obtainable by saponifying by means of an alcoholic caustic soda solution the ethylic ester cf. Beilstein, vol. IV, page 486). The solution remains clear and goods dyed in the usual manner are fast to rubbing. Without the addition of the aforesaid salt precipitates are formed and in consequence thereof goods similarly dyed are not fast to rubbing.
Example 9 In the same manner as described in the foregoing examples the ethylene-bis-(iminodiacetic) acid of the formula:
EOOC.H2C CH2.COOH
N.C:H4.N
HOOC.H2C CHQ-COOH may be used. It may be prepared either by saponifying the corresponding nitril or by acting with monochloro-acetic acid on ethylene diamine for instance in the following manner: 60 parts of ethylene diamine in an aqueous solution of 10% strength are mixed with 466 parts of the sodium salt of monochloroacetic acid and 212 parts of sodium carbonate and the mixture is heated at to C. for 8 to 10 hours. Then 470 parts of a hydrochloric acid of 20 B. are added. When cool, the aforesaid acid precipitates. It is dimculty soluble in cold water and may be recrystallized from water.
Example 10 Cotton goods are dyed as described in Example 6, but while adding per liter 2 grs. of the sodium salt of an acid of the formula:
which is obtainable in an analogous manner as the acids used in Examples 7 and 9 by acting with an excess of monochloroacetic acid on parahydroxyphenylalanine (Tyrosin).
Example 11 10 parts of the sulfuric acid ester of oleylalcohol (or of another synthetical deterging agent) are mixed with 15 parts of sodium perborate, 20 parts of sodium silicate, 15 parts of the sodium salt of the nitrolotriacetic acid and 40 parts of sodium chloride. In this manner a deterging agent very suitable for boiling washing processes which is clearly soluble even in hard water is obtained.
Gila-COOK Example 12 Example 13 To a solution containing per liter 10 grs. of barium chloride and 30 grs. of the sodium salt of the trimethylamine-tricarboxylic acid a con- 252. COMPOSlTlONS.
centrated solution of 10 grs. of sodium sulfate is added. At first the solution remains clear and becomes strongly turbid only after standing for some time. The barium sulfate which precipitates in a very fine state begins to sink down only after some hours.
Such a solution may be advantageously used for tarnishing artificial silk.
As it appears from the foregoing examples the most valuable compounds are aminocarboxylic acids of the general formula:
GHQ-CODE x-cin-000n wherein R stands for one of the radicles CHr-COOH -ci1iiN cm coon and C COOH c ll i X representing a member of the group consisting of CH2, H-C-alkyl, C=diall;yl, H-Cphenyl and C=cycloalkyl.
I claim:
1. Process for avoiding and rendering harmless precipitates formed from hard water salts, which comprises adding to hard water an alkali metal salt of the aminocarboxylic acid of the formula:
CH:.COOll 2. Process for avoiding and rendering harmless precipitates formed from hard water salts, which comprises adding to hard water an alkali metal salt of the aminocarboxylic acid of the formula:
3. The process of avoiding and rendering harmless precipitates of water insoluble metal salts which comprises adding to water containing salts of diand trivalent metals alkali metal salts of carboxylic acids of the general formula:
caicoon x-cnlcoon wherein R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R1 standing for a member of the group consisting of hydrogen and alkyl.
Cross Reference 4. The process of washing which comprises adding to hard water alkali metal salts of carboxylic acids of the general formula:
/CH:COOH x-omcoon wherein R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R2 standing for a member of the group consisting of hydrogen and alkyl, adding a Water-soluble detergent of the group consisting of salts of sulfonic acid derivatives of aliphatic and aromatic hydrocarbons, salts of acid sulfuric acid esters of higher aliphatic alcohols, salts of -condensation products of fatty acids with hydroxy alkyl sulfonic acids and salts of condensation products of fatty acids with amino alkyl sulfonic acids to the water and washing the materials to be cleansed with the water thus treated.
5. The process of washing which comprises adding to hard water alkali metal salts of carboxylic acids of the general formula:
/CH2COOII 5 N CBiCOOH wherein R stands for a member selected from the group consisting of the radicles R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R2 standing for a member of the group consisting of hydrogen and alkyl, adding a water-soluble soap to the water and washing the materials to be cleansed with the water thus treated.
6. As a washing composition a mixture consisting of a water-soluble soap and an alkali metal salt of a carboxylic acid of the general formula:
cmcoon x-crncoon Examiner wherein R stands for a member selected the group consisting of the radicles from R1 standing for a member of the group consisting of hydrogen, alkyl and phenyl and R: standing for a member of the group consisting of hydrogen and alkyl.
'7. As a washing composition a mixture consisting of a water-soluble detergent oi the group consisting of salts of suifonic acid derivatives of aliphatic and aromatic hydrocarbons, salts of acid sulfuric acid esters of higher aliphatic alcohols, salts of condensation products of fatty acids with. hydroxy allzyl sulfonic acids and salts of condensation products of fatty acids with amino alliyl SLfl-fOIliC acids and an alkali metal salt of a carboxylic acid of the general formula:
CHcC O OH x-cmc oon wherein R stands for a member selected from the group consisting of the radicles cilia ooii R1 ancling for a member of the group consisting of hydrogen, a kyl ncl phony; and R: standing for a member of the group consisting of hydrogen and allz'gl.
FERDINAND MUNZ.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US134737A US2130505A (en) | 1936-10-22 | 1937-04-03 | Polyamino carboxylic acids and process of making same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2240957X | 1935-10-30 |
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| Publication Number | Publication Date |
|---|---|
| US2240957A true US2240957A (en) | 1941-05-06 |
Family
ID=7991868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US107020A Expired - Lifetime US2240957A (en) | 1935-10-30 | 1936-10-22 | Process for avoiding and rendering harmless the precipitates of water insoluble metal salts |
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Cited By (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2524218A (en) * | 1946-03-28 | 1950-10-03 | Frederick C Bersworth | Washing composition |
| US2532391A (en) * | 1947-03-15 | 1950-12-05 | Frederick C Bersworth | Alkylene polyamine derivatives |
| US2542385A (en) * | 1946-10-12 | 1951-02-20 | Gen Aniline & Film Corp | Detergent composition |
| US2542831A (en) * | 1945-10-23 | 1951-02-20 | Socony Vacuum Oil Co Inc | Mineral oil composition and improving agent therefor |
| US2560839A (en) * | 1947-07-24 | 1951-07-17 | Gen Aniline & Film Corp | Detergent composition |
| US2564129A (en) * | 1951-08-14 | Cleaning and renewing used paint | ||
| US2583890A (en) * | 1945-05-02 | 1952-01-29 | Uetikon Chem Fab | Quantitative determination of metals |
| US2583891A (en) * | 1946-04-08 | 1952-01-29 | Uetikon Chem Fab | Quantitative determination of metals |
| US2589195A (en) * | 1949-03-14 | 1952-03-11 | Petrolite Corp | Processes for inhibiting scale deposition |
| US2606830A (en) * | 1949-03-08 | 1952-08-12 | Pittsburgh Coke & Chemical Co | Stable concentrated herbicidal compositions |
| US2606876A (en) * | 1952-08-12 | Compositions for stabilization of | ||
| US2657971A (en) * | 1951-12-10 | 1953-11-03 | Dental Perfection Company | Impression material |
| US2663704A (en) * | 1950-04-19 | 1953-12-22 | American Viscose Corp | Process and composition for producing improved viscose |
| US2777818A (en) * | 1954-10-08 | 1957-01-15 | United Chemical Corp Of New Me | Composition and method for controlling scale in oil wells |
| US2828262A (en) * | 1955-04-19 | 1958-03-25 | Exxon Research Engineering Co | Soap-salt complex thickened grease compositions |
| DE1042811B (en) * | 1953-02-13 | 1958-11-06 | California Research Corp | laundry detergent |
| US2868724A (en) * | 1954-02-12 | 1959-01-13 | Atlas Powder Co | Sequestering process |
| DE1049036B (en) * | 1953-03-18 | 1959-01-22 | California Research Corp | laundry detergent |
| US2921908A (en) * | 1956-07-02 | 1960-01-19 | Procter & Gamble | Sequestering composition containing a corrosion inhibitor |
| DE1102329B (en) * | 1959-10-01 | 1961-03-16 | Basf Ag | Washing-up liquid to prevent incrustations in textiles after washing |
| US2983684A (en) * | 1956-11-28 | 1961-05-09 | Wyandotte Chemicals Corp | Soap composition containing lime soap dispersant |
| US3095380A (en) * | 1958-07-14 | 1963-06-25 | Purex Corp Ltd | Composition for removal of heat scale and carbon deposits |
| US3211658A (en) * | 1961-03-24 | 1965-10-12 | Colgate Palmolive Co | Detergent composition with improved bleaching efficiency |
| US3228904A (en) * | 1962-05-03 | 1966-01-11 | Goodrich Co B F | Stabilization of synthetic polymers |
| US3293176A (en) * | 1964-04-01 | 1966-12-20 | Le Roy A White | Method of chelating with an ethergroup-containing sequestering agent |
| US3296027A (en) * | 1964-11-19 | 1967-01-03 | Nalco Chemical Co | Removal and inhibition of scale formation in steam generation |
| US3298956A (en) * | 1965-10-21 | 1967-01-17 | Monsanto Co | Lime soap dispersants |
| DE1244674B (en) * | 1956-12-19 | 1967-07-13 | Benckiser Gmbh Joh A | Process to avoid precipitation and discoloration and to mask iron in water |
| DE1258356B (en) * | 1956-08-09 | 1968-01-04 | Benckiser Gmbh Joh A | Process to avoid deposits and discoloration and to mask metal ions in alkaline waters |
| US3430641A (en) * | 1966-02-16 | 1969-03-04 | Nalco Chemical Co | Method of redispersing deposits |
| USRE28325E (en) * | 1958-10-08 | 1975-01-28 | Oh cooh | |
| US3965048A (en) * | 1974-03-29 | 1976-06-22 | The Drackett Company | Soap curd dissolving drain cleaner |
| US3966649A (en) * | 1972-09-28 | 1976-06-29 | Colgate-Palmolive Company | Liquid detergents containing chelidamic acids and salts thereof |
| US4216087A (en) * | 1978-12-18 | 1980-08-05 | The Dow Chemical Company | Scrubber scale prevention |
| US4245995A (en) * | 1977-02-25 | 1981-01-20 | Bayer Aktiengesellschaft | Stabilization of anionic indole dyestuffs |
| US4294914A (en) * | 1978-09-14 | 1981-10-13 | Eastman Kodak Company | Photographic bleach compositions and methods of photographic processing |
| USRE30796E (en) * | 1962-07-23 | 1981-11-17 | The Dow Chemical Co. | Scale removal, ferrous metal passivation and compositions therefor |
-
1936
- 1936-10-22 US US107020A patent/US2240957A/en not_active Expired - Lifetime
Cited By (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2606876A (en) * | 1952-08-12 | Compositions for stabilization of | ||
| US2564129A (en) * | 1951-08-14 | Cleaning and renewing used paint | ||
| US2583890A (en) * | 1945-05-02 | 1952-01-29 | Uetikon Chem Fab | Quantitative determination of metals |
| US2542831A (en) * | 1945-10-23 | 1951-02-20 | Socony Vacuum Oil Co Inc | Mineral oil composition and improving agent therefor |
| US2524218A (en) * | 1946-03-28 | 1950-10-03 | Frederick C Bersworth | Washing composition |
| US2583891A (en) * | 1946-04-08 | 1952-01-29 | Uetikon Chem Fab | Quantitative determination of metals |
| US2542385A (en) * | 1946-10-12 | 1951-02-20 | Gen Aniline & Film Corp | Detergent composition |
| US2532391A (en) * | 1947-03-15 | 1950-12-05 | Frederick C Bersworth | Alkylene polyamine derivatives |
| US2560839A (en) * | 1947-07-24 | 1951-07-17 | Gen Aniline & Film Corp | Detergent composition |
| US2606830A (en) * | 1949-03-08 | 1952-08-12 | Pittsburgh Coke & Chemical Co | Stable concentrated herbicidal compositions |
| US2589195A (en) * | 1949-03-14 | 1952-03-11 | Petrolite Corp | Processes for inhibiting scale deposition |
| US2663704A (en) * | 1950-04-19 | 1953-12-22 | American Viscose Corp | Process and composition for producing improved viscose |
| US2657971A (en) * | 1951-12-10 | 1953-11-03 | Dental Perfection Company | Impression material |
| DE1042811B (en) * | 1953-02-13 | 1958-11-06 | California Research Corp | laundry detergent |
| DE1049036B (en) * | 1953-03-18 | 1959-01-22 | California Research Corp | laundry detergent |
| US2868724A (en) * | 1954-02-12 | 1959-01-13 | Atlas Powder Co | Sequestering process |
| US2777818A (en) * | 1954-10-08 | 1957-01-15 | United Chemical Corp Of New Me | Composition and method for controlling scale in oil wells |
| US2828262A (en) * | 1955-04-19 | 1958-03-25 | Exxon Research Engineering Co | Soap-salt complex thickened grease compositions |
| US2921908A (en) * | 1956-07-02 | 1960-01-19 | Procter & Gamble | Sequestering composition containing a corrosion inhibitor |
| DE1258356B (en) * | 1956-08-09 | 1968-01-04 | Benckiser Gmbh Joh A | Process to avoid deposits and discoloration and to mask metal ions in alkaline waters |
| US2983684A (en) * | 1956-11-28 | 1961-05-09 | Wyandotte Chemicals Corp | Soap composition containing lime soap dispersant |
| DE1244674B (en) * | 1956-12-19 | 1967-07-13 | Benckiser Gmbh Joh A | Process to avoid precipitation and discoloration and to mask iron in water |
| US3095380A (en) * | 1958-07-14 | 1963-06-25 | Purex Corp Ltd | Composition for removal of heat scale and carbon deposits |
| USRE28325E (en) * | 1958-10-08 | 1975-01-28 | Oh cooh | |
| DE1102329B (en) * | 1959-10-01 | 1961-03-16 | Basf Ag | Washing-up liquid to prevent incrustations in textiles after washing |
| US3211658A (en) * | 1961-03-24 | 1965-10-12 | Colgate Palmolive Co | Detergent composition with improved bleaching efficiency |
| US3228904A (en) * | 1962-05-03 | 1966-01-11 | Goodrich Co B F | Stabilization of synthetic polymers |
| USRE30796E (en) * | 1962-07-23 | 1981-11-17 | The Dow Chemical Co. | Scale removal, ferrous metal passivation and compositions therefor |
| US3293176A (en) * | 1964-04-01 | 1966-12-20 | Le Roy A White | Method of chelating with an ethergroup-containing sequestering agent |
| US3296027A (en) * | 1964-11-19 | 1967-01-03 | Nalco Chemical Co | Removal and inhibition of scale formation in steam generation |
| US3298956A (en) * | 1965-10-21 | 1967-01-17 | Monsanto Co | Lime soap dispersants |
| US3430641A (en) * | 1966-02-16 | 1969-03-04 | Nalco Chemical Co | Method of redispersing deposits |
| US3966649A (en) * | 1972-09-28 | 1976-06-29 | Colgate-Palmolive Company | Liquid detergents containing chelidamic acids and salts thereof |
| US3965048A (en) * | 1974-03-29 | 1976-06-22 | The Drackett Company | Soap curd dissolving drain cleaner |
| US4245995A (en) * | 1977-02-25 | 1981-01-20 | Bayer Aktiengesellschaft | Stabilization of anionic indole dyestuffs |
| US4294914A (en) * | 1978-09-14 | 1981-10-13 | Eastman Kodak Company | Photographic bleach compositions and methods of photographic processing |
| US4216087A (en) * | 1978-12-18 | 1980-08-05 | The Dow Chemical Company | Scrubber scale prevention |
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