US1935946A - Candle manufacture - Google Patents

Candle manufacture Download PDF

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Publication number
US1935946A
US1935946A US606522A US60652232A US1935946A US 1935946 A US1935946 A US 1935946A US 606522 A US606522 A US 606522A US 60652232 A US60652232 A US 60652232A US 1935946 A US1935946 A US 1935946A
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US
United States
Prior art keywords
stearic acid
manufacture
candle
split
scale
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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 - Lifetime
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US606522A
Inventor
Egan James
Mills Victor
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.)
Procter and Gamble Co
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Procter and Gamble 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 Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US606522A priority Critical patent/US1935946A/en
Application granted granted Critical
Publication of US1935946A publication Critical patent/US1935946A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11C5/00Candles
    • C11C5/002Ingredients

Definitions

  • the manufacture of refined wax for candles has consisted of a graining operation in which the crystalline grains separating from the paraffin oil are retained within the plates of a filter press through which the grained material is passed.
  • the pressing operation results in the retention within the plates of a material which is known as scale, and has a melting point of from 121 to 127 degrees F. While the scale is a white product, it is too soft for use except with greatly increased percentages of commercial stearic acid.
  • the refining process of the paraffin wax suitable for candle manufacture from the scale increases the expense of candle manufacture, the price variation between 'scale and the refined wax being usually about to per pound.
  • the fatty material may .be split by any well known splitting process, such as the autoclave process, or that suggested by Twitchell or Petroff.
  • the splittin process as is well known, hydrolizes the fatty material and permits the glycerine to separate from the fatty acids.
  • the fatty acid recovered by this process is then distilled. It will have a stearic acid content of around 75%, and in admixture with commercial scale, candle material is formed which has a very fine grain and a determined resistance against cracking.
  • the percentage ofthe stearic acid, either commercial grade or synthetically produced, to be used with the parafiin wax may be varied to suit climatic conditions and the size of the candles to be made.
  • the art of candle manufacture which comprises admixing with paraflin scale a proportion of the split fatty acid from a hydrogenated oil in which the stearic acid content is considerably higher than the 45% normally occurring in commercial stearic acid, said stearic acid content being substantially in excess of 65%, and the percentage of said split fatty acid varying from 5 to 50% in the mixture.

Description

Patented Nov. 21, 1933 CANDLE MANUFACTURE James Egan, Staten Island, N. Y., and Victor Mills, Cincinnati, Ohio, assignors to The Proc-' ter & Gamble Company, Cincinnati, Ohio, a
corporation of Ohio No Drawing. Application April 20, 1932 Serial No. 606,522
'1 Claims. '(01. 87-21) v Our invention relates to the manufacture of candles, and particularly to the manufacture of candles from parafiin materials heretofore unavailable for use in such manufacture.
Stearic acid, as it is commercially known, and
as it has been commonly used in the manufacture of candles, is obtained from the saponification of tallow of high melting point, and con tains an average of approximately 45% stearic acid and 55% palmitic acid. Stearic acid has been used in the manufacture of candles by mixing about ten parts with about 90 parts of re-. fined paraflin wax. The parafiin wax required for candle manufacture has a melting point of from 128 to 138 degrees F.
The manufacture of refined wax for candles has consisted of a graining operation in which the crystalline grains separating from the paraffin oil are retained within the plates of a filter press through which the grained material is passed. The pressing operation results in the retention within the plates of a material which is known as scale, and has a melting point of from 121 to 127 degrees F. While the scale is a white product, it is too soft for use except with greatly increased percentages of commercial stearic acid. v
The refining process of the paraffin wax suitable for candle manufacture from the scale increases the expense of candle manufacture, the price variation between 'scale and the refined wax being usually about to per pound.
It is the object of our invention to utilize the less expensive scale for the manufacture of candles; and in order to secure good grade candle material having a fine opaque grain, superior to that obtainable from commercial stearic acid, we propose to mixwith the scale the split fatty acids resulting from products formed by hydrogenating natural oils having a high content of linolic, oleic or other unsaturated bodies.
In carrying out our process, we hydrogenate a suitable natural oil, such as cottonseed oil, until it has an iodine value of 5 or lower. The average titre of this hydrogenated product would be around degrees as against a variation of from 54 to 57 degrees for the best grade stearic acid.
After the oil is hydrogenated, the fatty material may .be split by any well known splitting process, such as the autoclave process, or that suggested by Twitchell or Petroff. The splittin process, as is well known, hydrolizes the fatty material and permits the glycerine to separate from the fatty acids.
The fatty acid recovered by this process is then distilled. It will have a stearic acid content of around 75%, and in admixture with commercial scale, candle material is formed which has a very fine grain and a determined resistance against cracking.
In order to explain the advantages of the use of our process over what had previously been suggested, we have in the first instance the use of a. paraffin product having softer physical characteristics and being less expensive in admixture with a split hydrogenated oil in which much less of the split hydrogenated oil is required to give the candle material a desired grain and resistance to cracking because of the much higher percentage of stearic acid present in the split hydrogenated oil. A further economy may be noted because the cost of preparation'of the stearic acid from hydrogenated oil is materially less than the cost of preparing stearic acid by the old well known tallow saponification process.
It should be understood that the percentage ofthe stearic acid, either commercial grade or synthetically produced, to be used with the parafiin wax may be varied to suit climatic conditions and the size of the candles to be made. We might state that as a specific example that from 5% to 10% of the split distilled fatty acid recovered .from hydrogenated oil can be satisfactorily used with 95% of scale. We may increase the proportion of the synthetic stearic acid however to as high as 50%.
While the use of split hydrogenated fatshas been suggested in the past, as far as we know the use of this split hydrogenated product has been merely suggested as a substitute for commercial stearic acid and not because its use would permit the use of a paraflin product which was materially cheaper in price.
If the candles are to be artificially colored, and
' if the candle stock is not to be the purest white,
which the stearic acid content is considerably higher than the 45% normally occurring in commercial stearic acid, said stearic acid content being substantially in excess of 3. The art of candle manufacture which comprises admixing with paraflin scale a proportion of the split fatty acid from a hydrogenated oil in which the stearic acid content is considerably higher than the 45% normally occurring in commercial stearic acid, said stearic acid content being substantially in excess of 65%, and the percentage of said split fatty acid varying from 5 to 50% in the mixture.
4. The art of candle manufacture which comprises using from to of paramn scale admixed with from 5 to 10% of a hydrogenated product having a stearic acid content of substantially in excess of 65%.
US606522A 1932-04-20 1932-04-20 Candle manufacture Expired - Lifetime US1935946A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US606522A US1935946A (en) 1932-04-20 1932-04-20 Candle manufacture

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US606522A US1935946A (en) 1932-04-20 1932-04-20 Candle manufacture

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US1935946A true US1935946A (en) 1933-11-21

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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2697926A (en) * 1949-07-29 1954-12-28 Standard Oil Dev Co Paraffin wax candle
US6503285B1 (en) 2001-05-11 2003-01-07 Cargill, Inc. Triacylglycerol based candle wax
US20030008257A1 (en) * 1998-08-12 2003-01-09 Indiana Soybean Board Vegetable lipid-based composition and candle
US20030017431A1 (en) * 2001-03-06 2003-01-23 Murphy Timothy A. Vegetable oil based wax compositions
US20030046860A1 (en) * 2001-08-02 2003-03-13 Archer Daniels Midland Co. Vegetable fat-based candles
US20030057599A1 (en) * 2001-09-25 2003-03-27 Murphy Timothy A. Triacylglycerol based wax compositions
US6645261B2 (en) 2000-03-06 2003-11-11 Cargill, Inc. Triacylglycerol-based alternative to paraffin wax
US20040088908A1 (en) * 2002-11-12 2004-05-13 Cargill, Inc Triacylglycerol based wax for use in candles
US20040088907A1 (en) * 2002-11-12 2004-05-13 Cargill, Inc. Triacylglycerol based wax for use in container candles
US6758869B2 (en) * 2000-02-02 2004-07-06 Cleanwax, Llp Non sooting paraffin containing candle
US20040221503A1 (en) * 2003-05-08 2004-11-11 Cargill, Incorporated Wax and wax-based products
US6852140B1 (en) 1999-09-24 2005-02-08 Cleanwax, Llc Low-soot, low-smoke renewable resource candle
US20060075679A1 (en) * 2004-10-13 2006-04-13 Cap Daniel S Acetylated wax compositions and articles containing them
US7588607B1 (en) 2005-03-16 2009-09-15 Daniel S. Cap Candlewax compositions with improved scent-throw
US8344052B2 (en) 2006-07-12 2013-01-01 Elevance Renewable Sciences, Inc. Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax
US8500826B2 (en) 2010-03-10 2013-08-06 Elevance Renewable Sciences, Inc. Lipid-based wax compositions substantially free of fat bloom and methods of making
US8551194B2 (en) 2007-05-30 2013-10-08 Elevance Renewable Sciences, Inc. Prilled waxes comprising small particles and smooth-sided compression candles made therefrom
US8603197B2 (en) 2007-02-16 2013-12-10 Elevance Renewable Sciences, Inc. Wax compositions and methods of preparing wax compositions
US8641814B2 (en) 2010-05-12 2014-02-04 Elevance Renewable Sciences, Inc. Natural oil based marking compositions and their methods of making
US8652221B2 (en) 2007-06-15 2014-02-18 Elevance Renewable Sciences, Inc. Hybrid wax compositions for use in compression molded wax articles such as candles
US8685118B2 (en) 2005-01-10 2014-04-01 Elevance Renewable Sciences, Inc. Candle and candle wax containing metathesis and metathesis-like products
US9139801B2 (en) 2011-07-10 2015-09-22 Elevance Renewable Sciences, Inc. Metallic soap compositions for various applications
US9249360B2 (en) 2010-07-09 2016-02-02 Elevance Renewable Sciences, Inc. Compositions derived from metathesized natural oils and amines and methods of making
US9458411B2 (en) 2010-11-23 2016-10-04 Cargill, Incorporated Lipid-based wax compositions substantially free of fat bloom and methods of making

Cited By (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2697926A (en) * 1949-07-29 1954-12-28 Standard Oil Dev Co Paraffin wax candle
US7731767B2 (en) 1998-08-12 2010-06-08 Indiana Soybean Board, Inc. Vegetable lipid-based composition and candle
US20030008257A1 (en) * 1998-08-12 2003-01-09 Indiana Soybean Board Vegetable lipid-based composition and candle
US7387649B2 (en) 1998-08-12 2008-06-17 Tao Bernard Y Vegetable lipid-based composition and candle
US6852140B1 (en) 1999-09-24 2005-02-08 Cleanwax, Llc Low-soot, low-smoke renewable resource candle
US6758869B2 (en) * 2000-02-02 2004-07-06 Cleanwax, Llp Non sooting paraffin containing candle
US8529924B2 (en) 2000-03-06 2013-09-10 Elevance Renewable Sciences, Inc. Triacyglycerol-based alternative to paraffin wax
US20040047886A1 (en) * 2000-03-06 2004-03-11 Cargill, Incorporated Triacylglycerol-based alternative to paraffin wax
US8202329B2 (en) 2000-03-06 2012-06-19 Elevance Renewable Sciences, Inc. Triacylglycerol-based alternative to paraffin wax
US6645261B2 (en) 2000-03-06 2003-11-11 Cargill, Inc. Triacylglycerol-based alternative to paraffin wax
US7217301B2 (en) 2000-03-06 2007-05-15 Cargill, Incorporated Triacylglycerol-based alternative to paraffin wax
US6824572B2 (en) 2001-03-06 2004-11-30 Cargill, Incorporated Vegetable oil based wax compositions
US20030017431A1 (en) * 2001-03-06 2003-01-23 Murphy Timothy A. Vegetable oil based wax compositions
US7462205B2 (en) 2001-05-11 2008-12-09 Elevance Renewable Sciences, Inc. Triacylglycerol based candle wax
US6770104B2 (en) 2001-05-11 2004-08-03 Cargill, Incorporated Triacylglycerol based candle wax
US8070833B2 (en) 2001-05-11 2011-12-06 Elevance Renewable Sciences, Inc. Triacyglycerol based candle wax
US20040221504A1 (en) * 2001-05-11 2004-11-11 Cargill, Incorporated Triacylglycerol based candle wax
US6503285B1 (en) 2001-05-11 2003-01-07 Cargill, Inc. Triacylglycerol based candle wax
US20030046860A1 (en) * 2001-08-02 2003-03-13 Archer Daniels Midland Co. Vegetable fat-based candles
US20030057599A1 (en) * 2001-09-25 2003-03-27 Murphy Timothy A. Triacylglycerol based wax compositions
US7128766B2 (en) 2001-09-25 2006-10-31 Cargill, Incorporated Triacylglycerol based wax compositions
US8021443B2 (en) 2001-09-25 2011-09-20 Elevance Renewable Sciences, Inc. Triacylglycerol based wax composition
US6773469B2 (en) 2002-11-12 2004-08-10 Cargill, Incorporated Triacylglycerol based wax for use in candles
US6797020B2 (en) 2002-11-12 2004-09-28 Cargill, Incorporated Triacylglycerol based wax for use in container candles
US20040088908A1 (en) * 2002-11-12 2004-05-13 Cargill, Inc Triacylglycerol based wax for use in candles
US20040088907A1 (en) * 2002-11-12 2004-05-13 Cargill, Inc. Triacylglycerol based wax for use in container candles
US20040221503A1 (en) * 2003-05-08 2004-11-11 Cargill, Incorporated Wax and wax-based products
US20060272200A1 (en) * 2003-05-08 2006-12-07 Cargill, Incorporated Wax and wax-based products
US7833294B2 (en) 2003-05-08 2010-11-16 Elevance Renewable Sciences, Inc. Wax and wax-based products
US7192457B2 (en) 2003-05-08 2007-03-20 Cargill, Incorporated Wax and wax-based products
US8157873B2 (en) 2003-05-08 2012-04-17 Elevance Renewable Sciences, Inc. Wax and wax-based products
US20060075679A1 (en) * 2004-10-13 2006-04-13 Cap Daniel S Acetylated wax compositions and articles containing them
US7510584B2 (en) 2004-10-13 2009-03-31 Daniel S. Cap Acetylated wax compositions and articles containing them
US8911515B2 (en) 2005-01-10 2014-12-16 Elevance Renewable Sciences, Inc. Candle and candle wax containing metathesis and metathesis-like products
US8685118B2 (en) 2005-01-10 2014-04-01 Elevance Renewable Sciences, Inc. Candle and candle wax containing metathesis and metathesis-like products
US7588607B1 (en) 2005-03-16 2009-09-15 Daniel S. Cap Candlewax compositions with improved scent-throw
US8344052B2 (en) 2006-07-12 2013-01-01 Elevance Renewable Sciences, Inc. Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax
US8603197B2 (en) 2007-02-16 2013-12-10 Elevance Renewable Sciences, Inc. Wax compositions and methods of preparing wax compositions
US8940090B2 (en) 2007-02-16 2015-01-27 Elevance Renewable Sciences, Inc. Wax compositions and methods of preparing wax compositions
US8551194B2 (en) 2007-05-30 2013-10-08 Elevance Renewable Sciences, Inc. Prilled waxes comprising small particles and smooth-sided compression candles made therefrom
US8652221B2 (en) 2007-06-15 2014-02-18 Elevance Renewable Sciences, Inc. Hybrid wax compositions for use in compression molded wax articles such as candles
US8500826B2 (en) 2010-03-10 2013-08-06 Elevance Renewable Sciences, Inc. Lipid-based wax compositions substantially free of fat bloom and methods of making
US8876919B2 (en) 2010-03-10 2014-11-04 Elevance Renewable Sciences, Inc. Lipid-based wax compositions substantially free of fat bloom and methods of making
US8641814B2 (en) 2010-05-12 2014-02-04 Elevance Renewable Sciences, Inc. Natural oil based marking compositions and their methods of making
US9249360B2 (en) 2010-07-09 2016-02-02 Elevance Renewable Sciences, Inc. Compositions derived from metathesized natural oils and amines and methods of making
US9867771B2 (en) 2010-07-09 2018-01-16 Elevance Renewable Sciences, Inc. Waxes derived from metathesized natural oils and amines and methods of making
US9458411B2 (en) 2010-11-23 2016-10-04 Cargill, Incorporated Lipid-based wax compositions substantially free of fat bloom and methods of making
US10179888B2 (en) 2010-11-23 2019-01-15 Cargill, Incorporated Lipid-based wax compositions substantially free of fat bloom and methods of making
US9139801B2 (en) 2011-07-10 2015-09-22 Elevance Renewable Sciences, Inc. Metallic soap compositions for various applications

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