GB477521A - Detergents - Google Patents

Detergents

Info

Publication number
GB477521A
GB477521A GB17700/36A GB1770036A GB477521A GB 477521 A GB477521 A GB 477521A GB 17700/36 A GB17700/36 A GB 17700/36A GB 1770036 A GB1770036 A GB 1770036A GB 477521 A GB477521 A GB 477521A
Authority
GB
United Kingdom
Prior art keywords
product
glycerine
sulphuric acid
water
sulphate
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
Application number
GB17700/36A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Colgate Palmolive Co
Original Assignee
Colgate Palmolive Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of GB477521A publication Critical patent/GB477521A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B3/00Refining fats or fatty oils
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/01Wetting, emulsifying, dispersing, or stabilizing agents
    • Y10S516/03Organic sulfoxy compound containing
    • Y10S516/04Protein or carboxylic compound containing

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Microbiology (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Fats And Perfumes (AREA)

Abstract

<PICT:0477521/IV/1> <PICT:0477521/IV/2> <PICT:0477521/IV/3> One molecular proportion of a fatty oil and one molecular proportion of anhydrous glycerine are reacted with such an excess of fuming sulphuric acid over the equivalent of three molecular proportions of 100 per cent sulphuric acid that the sulphuric acid remaining after the reaction has a concentration of not less than 95 per cent, and the product is neutralized without previous dilution, in the presence of a large excess of already neutralized material. The glycerine and fatty oil or the glycerine and excess fuming sulphuric acid may be first reacted together or the three components may be mixed simultaneously. The product may be prepared free from inorganic salts by extraction with alcohol, e.g. butyl alcohol, before or after the neutralization step or the sulphate free sodium, potassium, ammonium, triethanolamine and magnesium salts may be prepared from the calcium salt, the calcium being precipitated by means of carbon dioxide or a carbonate, phosphate or oxalate. The effect of adding solutions of the following salts to the pure and sulphate containing products is stated: calcium, barium, potassium, magnesium, aluminium, ferric and mercuric chlorides, ammonium and copper sulphates, lead acetate and silver nitrate. No turbidity or precipitate is given with hydrochloric acid, hard water and sea water. In an example, glycerine is treated with fuming sulphuric acid and the mixture is reacted with coconut oil. The glycerine and fuming sulphuric acid are pumped into a mixer 13 shown in Fig. 5, which consists of a cylindrical shell provided with paddles 24, 25 and 26 carried on a vertical shaft, and hollow annular members 27 and 28 through which cooling water is circulated. Each of the three upper paddles, as shown in Fig. 7, consists of a circular plate with four vanes extending helically above it to throw the liquid outwardly and four helical vanes below the plate to draw the liquid inwardly and propel it downwards to the underlying cooling element. The fourth paddle 25 is of similar construction but both upper and lower vanes force the liquid outwardly so that some is circulated to the top of the mixer. Before leaving the mixer by the opening 19, the reaction liquid passes cooling members 28 and paddles 26. The reaction liquid is treated with coconut oil in a second mixer similar in construction to the first, but the hollow annular members are supplied with heating water instead of cooling water and the reaction mixture is, in part returned to the top of the mixer by the second paddle, the upper and lower vanes of which throw the reaction mixture outwardly. The reaction mixture is passed to a neutralizer, Fig. 9, comprising cooling and mixing elements. Caustic soda solution enters by pipe 40 and the reaction mixture by the pipe 38, and the resulting neutralized product passes down through a cooling cylinder 41, being mixed by paddles 46 on a vertical shaft 44. The product then rises and is further cooled by the outer jacket 42; a portion is withdrawn through pipe 43. Additional cooling means is provided by a coil 50 and circulation is assisted by a large impeller 47 and deflecting members 48 and 49. A series of scrapers 51 and 52 removes any product that deposits upon the walls of the cooling chambers. The scrapers are attached to supports which are mounted upon a spider 57 which is rotated by a shaft 58. Springs 53, 54 press the scrapers against the walls of the cooling chambers. The supply of caustic soda is controlled by a device which continuously measures the pH value of the contents of the neutralizer. The product leaving the latter is subjected to a spray drying process, e.g. that described in Specification 291,041, [Class 91]. The following examples illustrate the use of the product as a detergent or emulsifying agent or soap substitute: (1) the product containing sodium sulphate is obtained in the form of flakes by drying it over a heated roll and is milled with water and a perfuming material containing eugenol; it is finally pressed into cakes; (2) the sodium sulphate free product is dried and formed into a bar; (3) a shaving cream free from alkalinity is formed by mixing the product with water, glycerine, stearic acid and a perfume; (4) a dental cream is formed by mixing the product with water, glycerine, calcium carbonate, starch, sodium benzoate and a flavouring material; dicalciumphosphate and magnesium hydroxide may also be present; (5) a face cream is formed by mixing the product with water, glycerine, stearic acid, mineral oil and perfume; (6) a shampoo is formed by drying, pulverizing and screening the product or by mixing the product with perfume and water; oils and bleaching or colouring agents may be present; (7) a mouthwash is formed by mixing the product with chlorthymol, methylsalicylate and water; (8) a solution of the product in water comprises a liquid soap to which oil or naphtha may be added; (9) the product in the form of its calcium salt is mixed with sugar, saccharine, sodium perborate, calcium carbonate and perfume. The products may also be mixed with soap, sodium carbonate, phosphate or silicate, germicides, phenol, cresol, resorcinol, silver nitrate, mercury bichloride, aluminium chloride, zinc sulphate, alum, isoeugenol, vanillin, methylanthranilate, pumice, whiting, feldspar, solvents, naphtha, talc, titanium dioxide, barium sulphate, chalk, pigments, dyes, deodorants, animal, vegetable or mineral oils, and starch. The use in the process of tallow, soy bean oil, palm oil, fish oils and garbage grease is specified. The Specification as open to inspection under Sect. 91 comprises generally the interaction of a fatty oil, anhydrous glycerine and fuming sulphuric acid. The use of glycol or other polyhydric alcohol instead of glycerine is mentioned, and also esterification with naphthenic and abietic acids and acids obtained by the oxidation of paraffin hydrocarbons. It is stated that the products may be mixed with emery, ether, alcohol, benzol, glycols and waxes. This subject-matter does not appear in the Specification as accepted.ALSO:One molecular proportion of a fatty oil and one molecular proportion of anhydrous glycerine are reacted with such an excess of fuming sulphuric acid over the equivalent of three molecular proportions of 100 per cent sulphuric acid that the sulphuric acid remaining after the reaction has a concentration of not less than 95 per cent, and the product is neutralized, without previous dilution, in the presence of a large excess of already neutralized material. The neutralized product may be used as a detergent or emulsifying agent or as a soap substitute. The glycerine and fatty oil or the glycerine and excess fuming sulphuric acid may be first reacted together or the three components may be mixed simultaneously. The product may be prepared free from inorganic salts by extraction with alcohol, e.g. butyl alcohol, before or after the neutralization step or the sulphate free sodium, potassium, ammonium, triethanolamine and magnesium salts may be prepared from the calcium salt, the calcium being precipitated by means of carbondioxide or a carbonate, phosphate or oxalate. The effect of adding solutions of the following salts to the pure and sulphate containing products is stated: calcium, barium, potassium, magnesium, aluminium, ferric and mercuric chlorides, ammonium and copper sulphates, lead acetate and silver nitrate. No turbidity or precipitate is given with hydrochloric acid, hard water and sea water. In an example, glycerine is treated with fuming sulphuric acid and the mixture is reacted with coconut oil. The products may be mixed with soap, sodium, carbonate, phosphate, or silicate, germicides, phenol, cresol, resorcinol, silver nitrate, mercurybichloride, aluminium chloride, zinc sulphate, alum, isoeugenol, vanillin, methyl-anthranilate, pumice, whiting, feldspar, solvents, naphtha, talc, titanium dioxide, barium sulphate, chalk, pigments, dyes, deodorants, animal vegetable or mineral oils, and starch. The use in the process of tallow, soya bean oil, palm oil, fish oils and garbage grease is mentioned. The Specification as open to inspection under Sect. 91 comprises generally the interaction of a fatty oil, anhydrous glycerine and fuming sulphuric acid. Naphthenic and abietic acids and acids obtained by the oxidation of paraffin hydrocarbons are specified and also the use, instead of glycerine, of glycols. It is stated that the products may be mixed with emery, ether, alcohol, benzol, glycols and waxes. This subject-matter does not appear in the Specification as accepted.ALSO:Products which may be used as soap substitutes are prepared by reacting one molecular proporition of a fatty oil and one molecular proportion of anhydrous glycerine with such an excess of fuming sulphuric acid over the equivalent of three molecular proportions of 100 per cent sulphuric acid that the sulphuric acid remaining after the reaction has a concentration of not less than 95 per cent and thereafter neutralizing the product, without previous dilution, in the presence of a large excess of already neutralized material. The glycerine and fatty oil or the glycerine and excess fuming sulphuric acid may be first reacted together or the three components may be mixed simultaneously. The product may be prepared free from inorganic salts by extraction with alcohol, e.g. butyl alcohol, before or after the neutralization step or the sulphate free sodium, potassium, ammonium, triethanolamine and magnesium salts may be prepared from the calcium salt, the calcium being precipitated by means of carbon dioxide or a carbonate, phosphate or oxalate. The effect of adding solutions of the following salts to the pure and sulphate containing products is stated; calcium, barium, potassium, magnesium, aluminium, ferric and
GB17700/36A 1935-06-27 1936-06-25 Detergents Expired GB477521A (en)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US201171XA 1935-06-27 1935-06-27
US709276XA 1935-06-27 1935-06-27
US2130362XA 1935-06-27 1935-06-27
US2130361XA 1935-06-27 1935-06-27
US477521XA 1935-06-27 1935-06-27
US201172XA 1935-06-27 1935-06-27
US28712A US2130362A (en) 1935-06-27 1935-06-27 Detergent and method of preparation
US28711A US2130361A (en) 1935-06-27 1935-06-27 Art of deterging
CH199777T 1936-06-19

Publications (1)

Publication Number Publication Date
GB477521A true GB477521A (en) 1937-12-28

Family

ID=32046213

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17700/36A Expired GB477521A (en) 1935-06-27 1936-06-25 Detergents

Country Status (4)

Country Link
US (2) US2130361A (en)
CH (2) CH201171A (en)
DE (1) DE709276C (en)
GB (1) GB477521A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423452A (en) * 1944-05-05 1947-07-08 Colgate Palmolive Peet Co Process for treating sprayed dried organic detergents
US2480579A (en) * 1943-10-21 1949-08-30 Colgate Palmolive Peet Co Detergent products and their preparation
US2489955A (en) * 1943-08-25 1949-11-29 Colgate Palmolive Peet Co Preparation of nondusting organic detergent compositions
US2678921A (en) * 1948-08-04 1954-05-18 Colgate Palmolive Co Process of producing a milled nonsoap detergent in bar form
US2704279A (en) * 1950-02-24 1955-03-15 Colgate Palmolive Co Toilet soap and process of preparing same
US2749315A (en) * 1951-04-28 1956-06-05 Colgate Palmolive Co Toilet detergent bar and process of preparing same
US2773835A (en) * 1951-11-16 1956-12-11 Colgate Palmolive Co Liquid shampoo composition
US2879231A (en) * 1950-10-13 1959-03-24 Colgate Palmolive Co Shampoo composition
US2945816A (en) * 1955-09-28 1960-07-19 Colgate Palmolive Co Process for preparing detergent bars

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423449A (en) * 1941-04-17 1947-07-08 Colgate Palmolive Peet Co Preparation of spray dried soap particles having only slight dustforming tendencies
US2423450A (en) * 1941-04-17 1947-07-08 Colgate Palmolive Peet Co Preparation of synthetic organic detergent particles having only slight dust-forming tendencies
US2428317A (en) * 1944-12-22 1947-09-30 Cleansing composition
US2506062A (en) * 1946-01-12 1950-05-02 Gen Aniline & Film Corp Fire extinguishing composition and method
US2529211A (en) * 1946-01-12 1950-11-07 Gen Aniline & Film Corp Fire extinguishing composition and method
US2868812A (en) * 1955-02-09 1959-01-13 Colgate Palmolive Co Manufacture of fatty acid monoesters of glycerol monosulfuric acid and salts thereof
US2844607A (en) * 1956-08-09 1958-07-22 Gen Aniline & Film Corp Process for the manufacture of sulpho-alkylesters of fatty acids
US4950440A (en) * 1987-09-14 1990-08-21 Colgate-Palmolive Company Process for the manufacture of high fatty acid monoglyceride monosulfate detergents
US4832876A (en) * 1987-09-14 1989-05-23 Colgate-Palmolive Company Process for the manufacture of higher fatty monoglyceride monosulfate detergents
SE535397C2 (en) 2009-08-12 2012-07-24 Alfa Laval Corp Ab A deodorizer, heat exchanger system comprising deodorizers and method of using its

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2489955A (en) * 1943-08-25 1949-11-29 Colgate Palmolive Peet Co Preparation of nondusting organic detergent compositions
US2480579A (en) * 1943-10-21 1949-08-30 Colgate Palmolive Peet Co Detergent products and their preparation
US2423452A (en) * 1944-05-05 1947-07-08 Colgate Palmolive Peet Co Process for treating sprayed dried organic detergents
US2678921A (en) * 1948-08-04 1954-05-18 Colgate Palmolive Co Process of producing a milled nonsoap detergent in bar form
US2704279A (en) * 1950-02-24 1955-03-15 Colgate Palmolive Co Toilet soap and process of preparing same
US2879231A (en) * 1950-10-13 1959-03-24 Colgate Palmolive Co Shampoo composition
US2749315A (en) * 1951-04-28 1956-06-05 Colgate Palmolive Co Toilet detergent bar and process of preparing same
US2773835A (en) * 1951-11-16 1956-12-11 Colgate Palmolive Co Liquid shampoo composition
US2945816A (en) * 1955-09-28 1960-07-19 Colgate Palmolive Co Process for preparing detergent bars

Also Published As

Publication number Publication date
US2130362A (en) 1938-09-20
CH201172A (en) 1938-11-15
US2130361A (en) 1938-09-20
DE709276C (en) 1941-08-12
CH201171A (en) 1938-11-15

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