US2301806A - Mineral wax composition - Google Patents

Mineral wax composition Download PDF

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Publication number
US2301806A
US2301806A US323122A US32312240A US2301806A US 2301806 A US2301806 A US 2301806A US 323122 A US323122 A US 323122A US 32312240 A US32312240 A US 32312240A US 2301806 A US2301806 A US 2301806A
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Prior art keywords
wax
color
formation
exposure
acids
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US323122A
Inventor
Lyle A Hamilton
Robert C Moran
Albert R Cattell
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ExxonMobil Oil Corp
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Socony Vacuum Oil Co Inc
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Priority to US323122A priority Critical patent/US2301806A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005Stabilisers against oxidation, heat, light, ozone

Definitions

  • This invention is directed to the stabilization of wax against the formation of deleterious color after long exposure to normal atmospheric and' light conditions under prolonged periods of time and has for its object the provision of a wax so stabilized by the addition thereto of certain ingredients not heretofore used for such purposes.
  • This invention is based upon the discovery that the esters of the aliphatic monohydric alcohols generally when mixed with wax in small amounts tend to materially increase the capability of the wax for resisting color deterioration under conditions of prolonged exposure to light at temperatures near atmospheric.
  • esters of aliphatic monohydric alcohols which may be used, several sub-classes appear to be particularly effective.
  • alkyl esters of aliphatic hydroxy acids such as for example dibutyl tartrate, amyl lactate, tributyl citrate and other similar esters.
  • alkyl esters of many dibasic acids we have found to be particularly effective and in particular in this general group have found effectiveness resident in the alkyl esters of phthalic acids, such as for example, diamyl phthalate.
  • the amounts in which these various inhibitive agents may be used will vary principally with the capability of .the inhibitive agent and with the type of exposure to which it is believed the product may be subjected, in general, however, the range of concentrations to be used will be from 0.01 to 5.0 weight percent with the preferred concentration being at about 1% by weight 01' the additive agent.
  • a white refined paraffin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an ester of an alkyl monohydric alcohol and an oxygen containing acid selected from the group consisting of aliphatic hydroxy acids, phthalic acid, and oxygen acids of phosphorus.
  • a white refined paraflin wax product inhibited. against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of from 0.01 to 5.0 weight per cent of an ester of an alkyl monohydric alcohol and an oxygen containing acid selected from the group consisting of aliphatichydroxy acids, phthalic acid, and oxygen acids of phos phorus.
  • a white refined paraflin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an aliphatic hydroxy acid.
  • a white refined paraflin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of phthalic acid.
  • a white refined parafiin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an oxygen acid of phosphorus.
  • a white refined paraflin wax product inaddition thereto of from 0.01 to 5.0 weight perpent of an alkyl ester of an oxygen acid of phosphorus.
  • a white refined paraffin wax product inhibited against the formation therein of delete rious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an acid selected from the group consisting of tartaric, lactic, and citric acids.
  • a white refined paraflln wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of diamyl phthalate.
  • a white refined paraffin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to-light by the addition thereto of a small amount of tri-; hutyl phosphate.

Description

' connection with food products.
Patented Nov. I 10, 1942 MINERAL WAX COMPOSITION Lyle A.
Hamilton and Robert C. Moran, Wenonah,
and Albert R. Cattell, Pitman, N. J assignors to Socony-Vacuum Oil Company, Incorporated,
New York, N. Y., a corporation of New York No Drawing. Application March 9, 1940, Serial No. 323,122
11 Claims.
Refined parafiin waxes in general require quite meticulous refining treatment to produce a wax which is stable against the formation of color bodies resulting in a yellowing of the wax over long periods of exposure of the wax to normal atmospheric and light conditions. This becomes particularly acute and is a controlling factor in the salability of the wax when the wax is utilized as a covering for, as a coating for, or otherwise in Since the formation of adverse color in the wax detracts materially from the appearance of the product with which it is associated, the color stability of the wax becomes a matter of very considerable importance over and beyond the value of the wax itself.
Numerous attempts have been made to increase the color stability of waxes by highly rigorous methods of refining, as, for example, treatment with sulfuric acids under extreme conditions.
This invention is directed to the stabilization of wax against the formation of deleterious color after long exposure to normal atmospheric and' light conditions under prolonged periods of time and has for its object the provision of a wax so stabilized by the addition thereto of certain ingredients not heretofore used for such purposes.
This invention is based upon the discovery that the esters of the aliphatic monohydric alcohols generally when mixed with wax in small amounts tend to materially increase the capability of the wax for resisting color deterioration under conditions of prolonged exposure to light at temperatures near atmospheric.
Of the various esters of aliphatic monohydric alcohols which may be used, several sub-classes appear to be particularly effective. For example, we may use the alkyl esters of aliphatic hydroxy acids such as for example dibutyl tartrate, amyl lactate, tributyl citrate and other similar esters. As a second class, we have found alkyl esters of many dibasic acids to be particularly effective and in particular in this general group have found effectiveness resident in the alkyl esters of phthalic acids, such as for example, diamyl phthalate. As a third class of useful esters we have found stabilization characteristics resident in alkyl esters of mineral acids specifically the oxygen acids of phosphorus, such as for example, tributyl phosphate.
To exemplify the color stabilizing effect of these various compositions, there are cited below results obtained in two tests. In each of these tests blocks of 126 F. A. S. T. M, melting point scale wax having the dimensions 6 in. x 1%; in. x /2 in.
with and without added inhibitors were exposed upon the roof of a building where they were called upon to withstand full sunlight exposure. In the first series of tests set forth in Table I, the duration of the exposure was 28 days. In the second series of tests, set forth in Table II, the duration of the exposure was 53 days.
Table I v [6" x 1%" x M blocks of 126 F, A. S. 'I. M. melting point scale wax, with and without added inhibitors-exposed on roof for 28 days] wax, with and without added inhibitors-exposed on root for 53 days] Samples Material added Conc g z Per cent Blank None Yellow. Samples lighter in Dibutyl tartrate. 1.0 color than blank Amyl lactate 1.0 after 53 days expo- Diamyl phthalate... 1.0 sure on roof. Tributyl phosphate. 1.0 No change.
On all of the above tests the samples after exposure were compared both with the blank and with similar blanks which had been protected from color deterioration. In all cases the color of the exposed sample was commercially improved over that of the uninhibited blank. In those tests wherein the color after test is noted No change," this means that the color of the inhibited test block after'the indicated exposure was exactly the same as the color of a fresh and unexposed block. Since no quantitative standards are in common use for expressing the color of wax, the data must necessarily be presented in the above form.
It is evident from the above tests that the inhibitors with which this invention is coneerned are capable of efiecting important changes in the liability of a commercial paraffn wax to the formation of deleterious color.
The amounts in which these various inhibitive agents may be used will vary principally with the capability of .the inhibitive agent and with the type of exposure to which it is believed the product may be subjected, in general, however, the range of concentrations to be used will be from 0.01 to 5.0 weight percent with the preferred concentration being at about 1% by weight 01' the additive agent.
We claim:
1. A white refined paraffin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an ester of an alkyl monohydric alcohol and an oxygen containing acid selected from the group consisting of aliphatic hydroxy acids, phthalic acid, and oxygen acids of phosphorus.
2. A white refined paraflin wax product inhibited. against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of from 0.01 to 5.0 weight per cent of an ester of an alkyl monohydric alcohol and an oxygen containing acid selected from the group consisting of aliphatichydroxy acids, phthalic acid, and oxygen acids of phos phorus.
3. A white refined paraflin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an aliphatic hydroxy acid.
4. A white refined paraflin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of phthalic acid.
5. A white refined parafiin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an oxygen acid of phosphorus.
6. A white refined paraflin wax product inaddition thereto of from 0.01 to 5.0 weight perpent of an alkyl ester of an oxygen acid of phosphorus.
9. A white refined paraffin wax product inhibited against the formation therein of delete rious color upon prolonged exposure to light by the addition thereto of a small amount of an alkyl ester of an acid selected from the group consisting of tartaric, lactic, and citric acids.
10. A white refined paraflln wax product inhibited against the formation therein of deleterious color upon prolonged exposure to light by the addition thereto of a small amount of diamyl phthalate. V
11. A white refined paraffin wax product inhibited against the formation therein of deleterious color upon prolonged exposure to-light by the addition thereto of a small amount of tri-; hutyl phosphate.
LYLE :a v2:"; TON.
ROBERT C. MORAN.
US323122A 1940-03-09 1940-03-09 Mineral wax composition Expired - Lifetime US2301806A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2625491A (en) * 1949-12-29 1953-01-13 Standard Oil Dev Co Stabilized wax composition
US2777776A (en) * 1954-05-03 1957-01-15 Atlantic Refining Co Free-flowing powdered waxes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2625491A (en) * 1949-12-29 1953-01-13 Standard Oil Dev Co Stabilized wax composition
US2777776A (en) * 1954-05-03 1957-01-15 Atlantic Refining Co Free-flowing powdered waxes

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