WO1996034077A1 - Candle - Google Patents
Candle Download PDFInfo
- Publication number
- WO1996034077A1 WO1996034077A1 PCT/US1996/005234 US9605234W WO9634077A1 WO 1996034077 A1 WO1996034077 A1 WO 1996034077A1 US 9605234 W US9605234 W US 9605234W WO 9634077 A1 WO9634077 A1 WO 9634077A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- candle
- diblock
- triblock
- copolymers
- gel
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims abstract description 53
- 229920000428 triblock copolymer Polymers 0.000 claims abstract description 31
- 229920000359 diblock copolymer Polymers 0.000 claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims description 49
- 239000000463 material Substances 0.000 claims description 39
- 229920001400 block copolymer Polymers 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 13
- 229930195733 hydrocarbon Natural products 0.000 claims description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 239000003205 fragrance Substances 0.000 claims description 8
- 229920006030 multiblock copolymer Polymers 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 4
- 229920001169 thermoplastic Polymers 0.000 claims 4
- 239000004416 thermosoftening plastic Substances 0.000 claims 4
- 229920001971 elastomer Polymers 0.000 abstract description 11
- 239000005060 rubber Substances 0.000 abstract description 10
- 239000002480 mineral oil Substances 0.000 abstract description 6
- 235000010446 mineral oil Nutrition 0.000 abstract description 6
- 239000004033 plastic Substances 0.000 abstract description 2
- 239000000499 gel Substances 0.000 description 53
- 239000003921 oil Substances 0.000 description 36
- 229920006122 polyamide resin Polymers 0.000 description 23
- 239000001993 wax Substances 0.000 description 17
- 229920002633 Kraton (polymer) Polymers 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 230000002441 reversible effect Effects 0.000 description 5
- 230000035900 sweating Effects 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 230000003796 beauty Effects 0.000 description 3
- 238000004939 coking Methods 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 210000004243 sweat Anatomy 0.000 description 3
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- -1 stearic acid compound Chemical class 0.000 description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 2
- 229920006345 thermoplastic polyamide Polymers 0.000 description 2
- JCYPECIVGRXBMO-UHFFFAOYSA-N 4-(dimethylamino)azobenzene Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=CC=CC=C1 JCYPECIVGRXBMO-UHFFFAOYSA-N 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 244000099147 Ananas comosus Species 0.000 description 1
- 235000007119 Ananas comosus Nutrition 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 244000297179 Syringa vulgaris Species 0.000 description 1
- 235000004338 Syringa vulgaris Nutrition 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 244000077233 Vaccinium uliginosum Species 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000008395 clarifying agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C5/00—Candles
- C11C5/002—Ingredients
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C5/00—Candles
- C11C5/002—Ingredients
- C11C5/004—Ingredients dyes, pigments; products giving a coloured flame
Definitions
- This invention relates generally to candles and more specifically to clear candles comprising a gel.
- the clear candle body of this invention comprises a heterophase thermally reversible mineral oil gel formed by a system of physically crosslinked block copolymers.
- the gel consistency may be controlled by varying the amount, ratio and types of certain copolymers, including diblock and triblock copolymers, so as to provide a gel which has desirable properties for a stable, safe, and attractive clear candle.
- the heat of the candle's flame melts a small pool of the candle body material around the base of the exposed portion of the wick, and this molten material is then drawn up through and along the wick by capillary attraction, to fuel the flame.
- a candle's melting point is critical, in that the candle material should liquefy at or below temperatures to which the candle's material can be raised by radiant heat from the candle flame. If the candle's melting temperature is too low, the candle will drip or, in an extreme case, the entire candle body will melt, dropping the wick into a pool of molten body material, with the potential that the surface of the pool could ignite.
- the candle body material burn with a flame that is both luminous and smokeless, and the odors that are produced by its combustion should not be unpleasant or intrusive.
- the candle body of this invention is made by the physical cross linking of co ⁇ polymers to form a gel which is heterophase
- heterophase as used herein means a 2-phase system, which comprises an "oil” phase and a “block co-polymer” phase, the two phases being separate chemically and on a micro scale physically, but indistinct on a macro scale physically), and thermally reversible (i.e., when the gel is heated, the chemical composition of the gel remains the same, only physical properties of the gel - such as viscosity - change).
- the clear candles disclosed in the prior art are typically manufactured with a thermoplastic polyamide resin which requires a chemical reaction to solidify the gel.
- polyamide resin materials of these prior candles when heated, melt into and form chemical substances different from the original monomers or chemical constituents.
- these polyamide resin based clear candles are not thermally reversible.
- a characteristic polyamide resin based candle is disclosed in United States patent 3,819,342 ("the '342 patent"). This patent discloses a transparent candle composition comprising a thermal plastic polyamide resin and a flammable solvent described as being capable of solubilizing the resin at a temperature below about 212°F, and forming a transparent gel-type structure.
- the solvent of the '342 patent is selected from the group consisting of unsaturated fatty acids, unsaturated fatty alcohols, saturated fatty alcohols, esters of fatty acids with polyhydric alcohols and glycerol, and mixtures thereof, and being present in amounts sufficient to gel the resin.
- Additional materials used in this candle are coloring, anti-flaring compounds, perfumes, clarifying agents. Examples of different anti-flaring compounds are listed, however, the requirement of an anti-flaring compound points out a most serious problem with all polyamide resin based candles. Specifically, polyamide resins are known to separate into layers, and, after separation, the top of the candle is covered with an oil layer that flashes when lit.
- the '289 patent discloses another clear candle that is chemically very similar to the devices of the '342 patent discussed above.
- the '289 patent discloses a candle composition which may be transparent or pastel shaded and which is allegedly adapted to incorporate perfumes without flashing during burning.
- the basic composition of the '289 patent comprises a thermoplastic polyamide resin formed from linoleic acid polymerized with polyamide compound; an alkolamide or alkanol; and a stearic acid compound.
- the '289 patent further describes the use of polyamide resins to allegedly help eliminate "sweating" and to provide a smoother and glossier finish.
- Sweating is the process whereby oils migrate out of the candle body to the surface, giving it a oily texture, and is most commonly caused by syneresis. Syneresis occurs when oil is physically squeezed out from the candle body because of excessive chemical crosslinking. Sweating is not only an aesthetic drawback, it can be a performance or safety problem as well. If a candle sweats, the oil on the surface is available to ignite, which can result in an uncontrolled or torch- like situation rather than a candle.
- the gel based candle of the present invention does not sweat or separate, because syneresis can be easily controlled by adjusting the ratio of diblock to triblock polymers to insure that all of the oil is entrained within a system of physically crosslinked copolymers.
- the '289 patent also discusses the optional addition of ionic surface agents to prevent "blooming" or fogging of the candle which would result in the loss of transparency. This is significant because another persistent complaint about commercially available polyamide resin based candles is that they are initially cloudy or they become cloudy over time. The addition of the ionic surface agents may help this problem in some cases, but it does not eliminate cloudiness in the polyamide resin based candles. In stark contrast, candle's made according to this invention start out clear, remain clear during burning, and do not "bloom” or fog over time.
- United States patent 3,645,705 discloses a transparent candle body material formed by combining a straight chain aliphatic amide with white mineral oil and alcohol.
- the '705 material is therefore, polyamide resin based, and is described as providing a molded, solid, and free standing product.
- the resin is mixed with natural oils to cause it to gel.
- This invention claims to be transparent as glass but slightly yellow due to the oil content. There is also a methyl ester added for hardness.
- the lack of pigment and/or dye is referred to numerous times in the disclosure, but there is no disclosure that the wax used is any different than the opaque paraffin wax used in normal candle making.
- the clear candle of the present invention is a true candle that burns and is consumed, and it is not a wax based candle but rather a gel based system of physically crosslinked copolymers.
- the clear candle of this application addresses and overcomes the structural, aesthetic and functional problems of prior art candles by providing a gel body of the present invention is formed by physically crosslinked block copolymers in a heterophase thermally reversible mineral oil gel.
- the paraffin wax or polyamide thermoplastic resin products known heretofore cannot provide a stable, clear candle having the structural and performance advantages as set forth herein.
- block copolymers which can be advantageously used as one or more components in the present invention.
- These block copolymers are described as gels or gelloid liquid extended polymer compositions which can comprise an intimate mixture of a block copolymer containing relatively hard blocks and relatively elastomeric blocks.
- the additional polymer or copolymer material of this disclosure is to have at least partial compatibility with and a higher glass transition softening or melting temperature than the hard blocks of the block copolymer, and at least 500 parts by weight of extender liquid per 100 parts of the block copolymer, the liquid being present to extend and soften the elastomeric blocks of the block copolymer.
- the extender liquid can be a hydrocarbon oil and/or a synthetic oil and the resulting gels or gelloid compositions are of the type which can be used in the clear candle of the present invention.
- the '603 publication is hereby incorporated by reference herein.
- gel material as described in United States patent 5,221,534 can also be utilized as the gel material for the body of the candle of the present invention.
- the '534 patent describes a health and beauty aid gel composition comprised of one or more health and beauty aid components, a mineral oil, and a blend of at least two different polymer members.
- the viscous, yet flowable material of the '534 patent was initially contemplated by the present applicant as a potential additive for standard wax based candles to enhance quality and to make them softer and less brittle, because the material of the '534 patent does not coke during burning. As a candle burns down into a container there may be insufficient oxygen at the bottom of the container to support complete combustion.
- Particles of incomplete combustion can thereby form on the upper inside edge of the container; coking typically takes the form of a black smudge-like ring around the top of the container.
- soot Particles of incomplete combustion
- coking typically takes the form of a black smudge-like ring around the top of the container.
- One object of the present invention is to form a non-coking candle which burns cleaner than both wax and polyamide resin based candles.
- the gel candle of the present invention may be starved for oxygen, the gel candle burns slower than wax and the oxygen demands are less, thus the potential for coking is obviated.
- Wax based and polyamide resin based candles burn more than 2 times faster than the gel material of this invention. In other words, the time to consume the entire clear gel candle takes more than twice as long as a standard paraffin wax, based on the same size and shape, candles.
- Another object of the present invention is to mold a candle, which when colored, does not fade, is more stable and longer lasting than both wax and polyamide resin based candles.
- Wax based and polyamide resin based candles are typically dyed with organic dyes which are sensitive to light. Pigments are not used in molded candles because they effect the burn of a wax based candle and they decrease the clarity of a polyamide resin based candle.
- a colored wax based or polyamide based candle sits on a table, or in any form of light, it's color begins to fade over time.
- the dye fades due to a chemical reaction of the organic dye with the organic candle body material in the presence of light and oxygen.
- the gel material of this invention does not chemically react with dyes and therefore, the color fades significantly less over time.
- a further object of the present invention is to form a candle which has a lower tendency to become brittle with age, as compared to wax based candles and polyamide resin based candles.
- Polyamide resin based candles become brittle as the oil component separates, or "sweats" out of the candle body.
- the gel candle body of this invention addresses this problem, as the gel is stable over time because the oil component is permanently entrained in the system of crosslinked copolymers. Furthermore, there are no chemical reactions occurring between components within the gel candle body so there is no gradual deterioration as is common with wax.
- Yet another object of the present invention is to form a candle which is thermally reversible.
- This thermal reversibility gives the clear candle of the instant invention significant process advantages over polyamide resin based candles.
- the polyamide resin based candles are solidified via a chemical polymerization reaction. This reaction cannot be reversed and all mixing, pouring and molding must be done at one time. Any mistakes in the molding process and a polyamide candle is ruined.
- the thermally reversibility of the clear candle of the present invention allows the easy mixing of color(s) and/or fragrance(s).
- the clear candle of the present invention may be poured into containers in one step or a series of steps.
- the manufacturer has great latitude in processing because after the gel is cooled it can be reheated to a fluid state, reworked, and recooled any number of times. Thermal reversibility allows the manufacturer to recycle material. For instance, if one candle container sells better than another, premade candles can be heated, removed from their old containers and poured into a more popular container. This recycling is not possible with a polyamide resin based candle. It is also an object of the present invention to form a candle which does not exhibit syneresis. Syneresis, the secretion of oil from a gel due to excessive crosslinking, is a serious problem with the polyamide resin based candles as discussed above.
- the polyamide based candles are chemically crosslinked to such a great extent that oil is exuded therefrom and oil layers can form.
- the presence of an oil layer on a candle is a serious safety concern.
- the gel candle body of the present invention is not prone to syneresis. Because physical, as opposed to chemical, crosslinking is involved the ratio, amount, and type of copolymers can be controlled to eliminate syneresis.
- the copolymers form three-dimensional networks or gels through physical crosslinks. Crosslinking in these block copolymers occurs due to the formation of submicroscopic particles of a particular block, referred to as domains.
- Crosslinking of the insoluble domains can be obtained by factors affecting the crosslink density of the networks including length of insoluble block domains, length of soluble block domains, and the number of crosslinkable sites.
- branched or star polymers will have more crosslinks than triblock or diblock polymers.
- the type of solvent or plasticizer to which the blocks are subjected will also affect these characteristics.
- a candle comprising: at least one wick; a container; a clear body; said wick being disposed through said body near the central axis of said body, said body being disposed in said container; and wherein said body is a clear gel comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, said composition including at least one diblock copolymer and at least one triblock copolymer.
- said at least one diblock copolymer and said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers, said diblock and triblock polymers comprising segments of styrene monomer units and rubber monomer units.
- a method of using a gel composition as a candle material said gel composition comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt.
- said at least one diblock copolymer and said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers, said diblock and triblock polymers comprising segments of styrene monomer units and rubber monomer units.
- the clear gel described herein has been found to be especially useful as a clear candle material, and preferably comprises a blend of polymers in combination with a hydrocarbon oil.
- the hydrocarbon oil can be a cosmetic grade hydrocarbon oil (natural or synthetic) and more preferably it is white oil.
- Such hydrocarbon oils should have characteristics which will cause them to remain liquid at temperatures ranging from 0°C up to about 200°C for almost all applications, and may be a paraffinic oil, a naphthenic oil, natural mineral oil or the like.
- the blend of polymers preferably comprises at least two components selected from the group consisting of diblock copolymers, triblock copolymers, radial copolymers, multiblock polymers and mixtures thereof. It is required that at least one diblock and at least one triblock copolymer be present in the blend.
- Commercially available thermoplastic rubber type polymers which are especially useful in forming the compositions of the present invention are sold under the trademark Kraton® by
- the Kraton® rubber polymers are described as elastomers which have an unusual combination of high strength and low viscosity and a unique molecular structure of linear diblock, triblock and radial polymers. Each molecule of the Kraton® rubber is believed to consist of block segments of styrene monomer units and rubber monomer units and each block segment may consist of 100 monomer units or more. The most common structure is the linear ABA block type; styrene-butadiene-styrene (SBS) and styrene-isoprene-styrene (SIS), the Kraton® D rubber series.
- SBS styrene-butadiene-styrene
- SIS styrene-isoprene-styrene
- a second generation polymer of this series is the Kraton® G series which are styrene-ethylene-butylene-styrene type (S-EB-S) polymers.
- Diblock polymers include the ABA type and the SB, styrene-ethylenepropylene (S-EP) and (S-EB).
- S-EP styrene-ethylenepropylene
- S-EB styrene-ethylenepropylene
- the ABA structure of the Kraton® rubber molecule has polystyrene endblocks and elastomeric midblocks.
- This series of polymers is sold commercially and indicated as being major compounding ingredients or additives in adhesives, sealants and coatings, asphalt modification for roads and roofing, polymer modification, thermoset modification, and oil modification including use as viscosity index improvers, greases and gels.
- the Kraton® G rubbers are indicated as being compatible with paraffinic and naphthionic oils and the triblock copolymers are reported as taking up more than 20 times their weight in oil to make a product which can vary in consistency from a "Jello” to a strong elastic rubbery material depending on the grade and concentration of the rubber.
- a preferred clear candle body composition of the instant invention is prepared by blending into the hydrocarbon oil the mixture or blend of diblock and triblock or other copolymers in the desired amounts. The amounts of each copolymer and the amount of the mixture contained in the hydrocarbon oil will determine the final form of the gel. Care must be taken to insure the ratio, amount and type of ingredients are correct to yield a clear semi-solid gel.
- the semi-solid gel is the candle "body.”
- the gel is formed by blending the polymers and oil and heating them to between about 50° to 90° C to dissolve the polymer blend in the oil. Mixing may be carried out in any conventional manner. On cooling, the gel forms. Fragrance(s) and/or color(s) may be added at any time prior to cooling. Alternatively, a formed gel can be heated to reform the solution, upon which the fragrance(s) and/or color(s) may be added, and the gel allowed to reform on cooling. The resulting gel is preferably free standing at room temperature (the candle "body") and must be heated to about 200° Fahrenheit (93.3°C), plus or minus 10° before it flows easily. After the fragrance(s) and/or color(s) are mixed into the material it is poured into a container. Typical colors and fragrances which can be used in preferred embodiments are listed in tables 1 and 2.
- the container for a candle made hereunder can comprise any of a variety of devices which can contain the gel, do not burn, and do not melt.
- a faceted glass container can be used for aesthetic purposes. While it is contemplated that a clear candle made according to the present invention could be provided without a container, due to the gel-like nature of the candle itself, and its potential flowability when heated, it is preferred that such candles include an appropriate container.
- wick is placed in the candle body before the gel firms up.
- the term "wick” as used herein means any filamentary body which is sufficiently sturdy, which will bum with a flame, and which is capable of drawing up the molten candle material by capillary action.
- the wick can be any properly sized commercially available wick.
- an appropriately sized Atkins and Pierce 60/40/18 type wick, saturated with a high molecular weight microcrystalline wax can be used.
- more than one wick may be used in a single candle according to the present invention.
- the blend of copolymers used in the preferred formulation of the clear candle body is a mixture of diblock copolymers and triblock copolymers.
- Each polymer contains at least two incompatible segments, for example at least one hard and one soft segment. In general in the diblock polymer, segments will be sequential with respect to hard and soft segments. In a triblock polymer, the segment ratio is two hard/ one soft, two hard/one soft, etc. (i.e. a 2-1-2-1 copolymer).
- the multiblock polymers can contain any combination of hard and soft segments. In the clear candle composition, however, there must always be present at least one diblock and one triblock copolymers, and the combination must also provide both the hard and soft characteristics necessary for the composition. These characteristics are necessary in order to provide the controlled syneresis which is an essential part of the present invention.
- the body of the clear candle is thereby preferably provided in a gel form comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of: diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, there being present at least one diblock copolymer and at least one triblock copolymer. While the precise ratio of diblock and triblock copolymers can be varied to provide varying characteristics to the gel, it has been found that both must be present.
- said at least one diblock copolymer and at least one triblock copolymer comprise from about 1 to 99 wt.
- the diblock copolymer forms from about 1 to 3 weight percent of the blend of polymers, while the triblock copolymer forms from about 97 to 99 weight percent of the blend of polymers. It has been found that having a disproportionately large part of the triblock in comparison to the diblock, tends to make the material more gel-like and less prone to crumbling.
- the diblock or triblock copolymers should also have copolymers comprising block segments of styrene monomer units and mbber monomer units.
- the diameter of the gel candle body is preferably less than 3 inches (7.6 cm) as it has been observed that if the gel candle is larger, the heat of the wick may not melt the entire top of the candle surface. This will leave some gel material around the edges unburned and the candle will bu down the middle, leaving the edges of the container coated with some of the material. This is not preferred for aesthetic reasons, and due to the general wasteful nature of such performance.
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Abstract
A clear candle made from a gel comprising mineral oil containing blends of diblock and triblock copolymers based on synthetic thermal plastic rubbers. The clear candle is stable, does not separate, and does not flash when burned. The candle, although free standing at room temperature, will preferably be supplied in a container, and it may be colored and/or scented.
Description
CANDLE
Mohamed Elsamaloty
This is a continuation-in-part application of application Serial No. 08/429,606 filed April 27, 1995.
FIELD OF THE INVENTION
This invention relates generally to candles and more specifically to clear candles comprising a gel. The clear candle body of this invention comprises a heterophase thermally reversible mineral oil gel formed by a system of physically crosslinked block copolymers. The gel consistency may be controlled by varying the amount, ratio and types of certain copolymers, including diblock and triblock copolymers, so as to provide a gel which has desirable properties for a stable, safe, and attractive clear candle.
BACKGROUND OF THE INVENTION
While the burning of a candle might appear to be simple and uninvolved, in fact, the process that takes place in the burning of a candle imposes rather stringent requirements upon the candle body material. At the outset, a typical wax candle body
must be rigid enough to support itself (or be supported), in a relatively long wick filament, but it should not be excessively brittle at low room temperatures.
With respect to the actual burning of the candle, the heat of the candle's flame melts a small pool of the candle body material around the base of the exposed portion of the wick, and this molten material is then drawn up through and along the wick by capillary attraction, to fuel the flame. A candle's melting point is critical, in that the candle material should liquefy at or below temperatures to which the candle's material can be raised by radiant heat from the candle flame. If the candle's melting temperature is too low, the candle will drip or, in an extreme case, the entire candle body will melt, dropping the wick into a pool of molten body material, with the potential that the surface of the pool could ignite. If too high a temperature is required to melt the body material, the flame will be starved because insufficient fuel will be drawn up through the wick, with the result that the flame will be too small to maintain itself. Moreover, when molten, the candle body material must have a relatively low viscosity to insure that it will be capable of being drawn up through the wick by capillary action. In addition to meeting the above requirements, it is preferred that the candle body material burn with a flame that is both luminous and smokeless, and the odors that are produced by its combustion should not be unpleasant or intrusive.
Heretofore no composition that meets all these requirements has been transparent or clear (the terms "clear" and "transparent" are used interchangeably herein and connote a substantial absence of cloudiness/obscurity, so that the product
features an ability to let light pass through in a substantially unobstructed manner, and an ability to have colorant added to the composition without the loss of the absence of cloudiness/obscurity or of the ability to let light pass through in a fairly unobstructed manner). Although clear candles have been disclosed in the prior art, none of these formulations have fulfilled all of the above described requirements of a candle in general, nor have they possessed all of the benefits of the clear candle of this invention. The present invention has an objective of providing a clear candle with a soft rubbery consistency which does not change or harden, and which possesses all of the necessary characteristics of a candle and which, moreover, is truly transparent.
The candle body of this invention is made by the physical cross linking of co¬ polymers to form a gel which is heterophase ("heterophase" as used herein means a 2-phase system, which comprises an "oil" phase and a "block co-polymer" phase, the two phases being separate chemically and on a micro scale physically, but indistinct on a macro scale physically), and thermally reversible (i.e., when the gel is heated, the chemical composition of the gel remains the same, only physical properties of the gel - such as viscosity - change). The clear candles disclosed in the prior art are typically manufactured with a thermoplastic polyamide resin which requires a chemical reaction to solidify the gel. The polyamide resin materials of these prior candles, when heated, melt into and form chemical substances different from the original monomers or chemical constituents. Thus, these polyamide resin based clear candles are not thermally reversible.
A characteristic polyamide resin based candle is disclosed in United States patent 3,819,342 ("the '342 patent"). This patent discloses a transparent candle composition comprising a thermal plastic polyamide resin and a flammable solvent described as being capable of solubilizing the resin at a temperature below about 212°F, and forming a transparent gel-type structure. The solvent of the '342 patent is selected from the group consisting of unsaturated fatty acids, unsaturated fatty alcohols, saturated fatty alcohols, esters of fatty acids with polyhydric alcohols and glycerol, and mixtures thereof, and being present in amounts sufficient to gel the resin. Additional materials used in this candle are coloring, anti-flaring compounds, perfumes, clarifying agents. Examples of different anti-flaring compounds are listed, however, the requirement of an anti-flaring compound points out a most serious problem with all polyamide resin based candles. Specifically, polyamide resins are known to separate into layers, and, after separation, the top of the candle is covered with an oil layer that flashes when lit. This flashing can obviously be hazardous and is functionally inconsistent with a candle's natural function of providing reliable, consistent lighting. Clear candles made in accordance with this invention have the advantage of being completely stable over time. They will not separate into layers as prior art candles would, and thus there is no excess fluid available to flash.
United States Patent 3,615,289 ("the '289 patent"), discloses another clear candle that is chemically very similar to the devices of the '342 patent discussed above. The '289 patent discloses a candle composition which may be transparent or pastel shaded and which is allegedly adapted to incorporate perfumes without flashing during burning. The basic composition of the '289 patent comprises a thermoplastic
polyamide resin formed from linoleic acid polymerized with polyamide compound; an alkolamide or alkanol; and a stearic acid compound. The '289 patent further describes the use of polyamide resins to allegedly help eliminate "sweating" and to provide a smoother and glossier finish. Sweating is the process whereby oils migrate out of the candle body to the surface, giving it a oily texture, and is most commonly caused by syneresis. Syneresis occurs when oil is physically squeezed out from the candle body because of excessive chemical crosslinking. Sweating is not only an aesthetic drawback, it can be a performance or safety problem as well. If a candle sweats, the oil on the surface is available to ignite, which can result in an uncontrolled or torch- like situation rather than a candle.
Practical experience with, and laboratory testing of, the '289 and '342 candles has indicated that separation was a consistent and serious problem. Sweating also occurred in these candles, but the amount of oil secreted was small with respect to the large pool of oil that forms on the top of the candles after phase separation. The gel based candle of the present invention does not sweat or separate, because syneresis can be easily controlled by adjusting the ratio of diblock to triblock polymers to insure that all of the oil is entrained within a system of physically crosslinked copolymers.
The '289 patent also discusses the optional addition of ionic surface agents to prevent "blooming" or fogging of the candle which would result in the loss of transparency. This is significant because another persistent complaint about commercially available polyamide resin based candles is that they are initially cloudy or they become cloudy over time. The addition of the ionic surface agents may help
this problem in some cases, but it does not eliminate cloudiness in the polyamide resin based candles. In stark contrast, candle's made according to this invention start out clear, remain clear during burning, and do not "bloom" or fog over time.
United States patent 3,645,705 discloses a transparent candle body material formed by combining a straight chain aliphatic amide with white mineral oil and alcohol. The '705 material is therefore, polyamide resin based, and is described as providing a molded, solid, and free standing product. The resin is mixed with natural oils to cause it to gel. This invention claims to be transparent as glass but slightly yellow due to the oil content. There is also a methyl ester added for hardness. The
'705 patent is, however, similar in composition to the '342 and '289 patents and has the same structural and functional problems associated with it, and is therefore chemically as well as physically distinct from the present invention.
United States patent 3,741,711 ("the '711 patent"), discloses a clear, undyed and unpigmented wax based "candle." However, a closer reading of this patent indicates that the invention is a reusable "candle holder" and not a "candle". Particularly, the '711 patent discloses a multilayer holder with a decorated outer surface. The disclosure further states that the candle body has "an illuminous glow throughout the body of the candle ... when the candle is being burned.". There are, however, no compositions claimed, or disclosed, other than wax. In this particular patent, "clear" apparently means, a wax that is undyed and unpigmented. The lack of pigment and/or dye is referred to numerous times in the disclosure, but there is no disclosure that the wax used is any different than the opaque paraffin wax used in
normal candle making. In contrast, the clear candle of the present invention is a true candle that burns and is consumed, and it is not a wax based candle but rather a gel based system of physically crosslinked copolymers.
Thus, in general, the clear candle of this application addresses and overcomes the structural, aesthetic and functional problems of prior art candles by providing a gel body of the present invention is formed by physically crosslinked block copolymers in a heterophase thermally reversible mineral oil gel. The paraffin wax or polyamide thermoplastic resin products known heretofore cannot provide a stable, clear candle having the structural and performance advantages as set forth herein.
PCT Application No. WO 88-00603 ("the '603 publication"), published Jan. 28, 1988, describes block copolymers which can be advantageously used as one or more components in the present invention. These block copolymers are described as gels or gelloid liquid extended polymer compositions which can comprise an intimate mixture of a block copolymer containing relatively hard blocks and relatively elastomeric blocks. The additional polymer or copolymer material of this disclosure is to have at least partial compatibility with and a higher glass transition softening or melting temperature than the hard blocks of the block copolymer, and at least 500 parts by weight of extender liquid per 100 parts of the block copolymer, the liquid being present to extend and soften the elastomeric blocks of the block copolymer. The extender liquid can be a hydrocarbon oil and/or a synthetic oil and the resulting gels or gelloid compositions are of the type which can be used in the clear candle of the present invention. However, there is no teaching, or suggestion in the '603 publication
of the potential for using these materials in a candle, let alone to form a clear candle. The '603 publication is hereby incorporated by reference herein.
Similarly, gel material as described in United States patent 5,221,534 ("the '534 patent") can also be utilized as the gel material for the body of the candle of the present invention. The '534 patent describes a health and beauty aid gel composition comprised of one or more health and beauty aid components, a mineral oil, and a blend of at least two different polymer members. The viscous, yet flowable material of the '534 patent was initially contemplated by the present applicant as a potential additive for standard wax based candles to enhance quality and to make them softer and less brittle, because the material of the '534 patent does not coke during burning. As a candle burns down into a container there may be insufficient oxygen at the bottom of the container to support complete combustion. Particles of incomplete combustion (known as soot or coke) can thereby form on the upper inside edge of the container; coking typically takes the form of a black smudge-like ring around the top of the container. During testing, however, it was observed that the material of the '534 patent began to separate into layers when it sat for a short period of time. Also, the material flashed when the wick placed in it was lit. These characteristics made this material unsuitable for the purpose of a candle additive.
During testing however, a reformulated, more gel-like version of the material of the '534 patent was checked for possible use as an additive. The amount of the triblock polymers was increased so as to make the material more gel-like. While the product was determined to be of no interest as a candle additive, the testing led to an important discovery. The reformulated material was heated until it flowed, it was poured into a jar. A wick was then placed into it. and the sample was burned. There was no separation into phases, no sweating, and the material did not flash when burned. Surprisingly and quite unexpectedly, it was discovered that the experimental candle was transparent, it's body glowed when lit, and it did not discolor upon burning. The transparent nature of the candle made it extremely attractive.
Although this reformulated version of the '534 patent forms an excellent clear candle, it is at the same time rendered less suitable for its original purpose as a carrier for health and beauty aid compositions because of its gel (semi-solid) form. Importantly, there is no teaching or suggestion in the '534 patent of the potential for using this material as a candle. The disclosure of the '534 patent is hereby incorporated herein by reference.
SUMMARY OF THE INVENTION
While not exclusive, the following describes some of the important features and objectives of the present invention.
One object of the present invention is to form a non-coking candle which burns cleaner than both wax and polyamide resin based candles. Although it is possible for the gel candle of the present invention to be starved for oxygen, the gel candle burns slower than wax and the oxygen demands are less, thus the potential for coking is obviated.
It is yet another object of the present invention to form a candle which has a slower burn rate than a normal paraffin wax candle or a polyamide resin based candle.
Wax based and polyamide resin based candles burn more than 2 times faster than the gel material of this invention. In other words, the time to consume the entire clear gel candle takes more than twice as long as a standard paraffin wax, based on the same size and shape, candles.
Thus, it is a further object of the present invention to form a candle which is longer lasting than wax based and polyamide resin based candles.
Another object of the present invention is to mold a candle, which when colored, does not fade, is more stable and longer lasting than both wax and polyamide resin based candles. Wax based and polyamide resin based candles are typically dyed with organic dyes which are sensitive to light. Pigments are not used in molded
candles because they effect the burn of a wax based candle and they decrease the clarity of a polyamide resin based candle. When a colored wax based or polyamide based candle sits on a table, or in any form of light, it's color begins to fade over time. The dye fades due to a chemical reaction of the organic dye with the organic candle body material in the presence of light and oxygen. The gel material of this invention does not chemically react with dyes and therefore, the color fades significantly less over time.
A further object of the present invention is to form a candle which has a lower tendency to become brittle with age, as compared to wax based candles and polyamide resin based candles. Polyamide resin based candles become brittle as the oil component separates, or "sweats" out of the candle body. The gel candle body of this invention addresses this problem, as the gel is stable over time because the oil component is permanently entrained in the system of crosslinked copolymers. Furthermore, there are no chemical reactions occurring between components within the gel candle body so there is no gradual deterioration as is common with wax.
Yet another object of the present invention is to form a candle which is thermally reversible. This thermal reversibility gives the clear candle of the instant invention significant process advantages over polyamide resin based candles. The polyamide resin based candles are solidified via a chemical polymerization reaction. This reaction cannot be reversed and all mixing, pouring and molding must be done at one time. Any mistakes in the molding process and a polyamide candle is ruined. The thermally reversibility of the clear candle of the present invention allows the easy mixing of color(s) and/or fragrance(s). Furthermore, the clear candle of the present invention may be poured into containers in one step or a series of steps. The manufacturer has great latitude in processing because after the gel is cooled it can be reheated to a fluid state, reworked, and recooled any number of times. Thermal reversibility allows the manufacturer to recycle material. For instance, if one candle container sells better than another, premade candles can be heated, removed from their old containers and poured into a more popular container. This recycling is not possible with a polyamide resin based candle.
It is also an object of the present invention to form a candle which does not exhibit syneresis. Syneresis, the secretion of oil from a gel due to excessive crosslinking, is a serious problem with the polyamide resin based candles as discussed above. The polyamide based candles are chemically crosslinked to such a great extent that oil is exuded therefrom and oil layers can form. The presence of an oil layer on a candle is a serious safety concern. The gel candle body of the present invention is not prone to syneresis. Because physical, as opposed to chemical, crosslinking is involved the ratio, amount, and type of copolymers can be controlled to eliminate syneresis. The copolymers form three-dimensional networks or gels through physical crosslinks. Crosslinking in these block copolymers occurs due to the formation of submicroscopic particles of a particular block, referred to as domains. Crosslinking of the insoluble domains can be obtained by factors affecting the crosslink density of the networks including length of insoluble block domains, length of soluble block domains, and the number of crosslinkable sites. For example, branched or star polymers will have more crosslinks than triblock or diblock polymers. The type of solvent or plasticizer to which the blocks are subjected will also affect these characteristics.
The above objects are achieved in accordance with the first aspect of the present invention which is a candle comprising: at least one wick; a container; a clear body; said wick being disposed through said body near the central axis of said body, said body being disposed in said container; and wherein said body is a clear gel comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, said composition including at least one diblock copolymer and at least one triblock copolymer. Preferably, said at least one diblock copolymer and said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers, said diblock and triblock polymers comprising segments of styrene monomer units and rubber monomer units.
In accordance with another aspect of the present invention, there is disclosed a method of using a gel composition as a candle material, said gel composition comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, with the proviso that there be contained in the composition at least one diblock copolymer and at least one triblock copolymer. Preferably, said at least one diblock copolymer and said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers, said diblock and triblock polymers comprising segments of styrene monomer units and rubber monomer units.
DETAILED DESCRIPTION OF INVENTION
The preferred embodiments of the present invention will now be described in greater detail below.
The clear gel described herein has been found to be especially useful as a clear candle material, and preferably comprises a blend of polymers in combination with a hydrocarbon oil. The hydrocarbon oil can be a cosmetic grade hydrocarbon oil (natural or synthetic) and more preferably it is white oil. Such hydrocarbon oils should have characteristics which will cause them to remain liquid at temperatures ranging from 0°C up to about 200°C for almost all applications, and may be a paraffinic oil, a naphthenic oil, natural mineral oil or the like.
The blend of polymers preferably comprises at least two components selected from the group consisting of diblock copolymers, triblock copolymers, radial copolymers, multiblock polymers and mixtures thereof. It is required that at least one diblock and at least one triblock copolymer be present in the blend. Commercially available thermoplastic rubber type polymers which are especially useful in forming the compositions of the present invention are sold under the trademark Kraton® by
Shell Chemical Company. The Kraton® rubber polymers are described as elastomers which have an unusual combination of high strength and low viscosity and a unique
molecular structure of linear diblock, triblock and radial polymers. Each molecule of the Kraton® rubber is believed to consist of block segments of styrene monomer units and rubber monomer units and each block segment may consist of 100 monomer units or more. The most common structure is the linear ABA block type; styrene-butadiene-styrene (SBS) and styrene-isoprene-styrene (SIS), the Kraton® D rubber series. A second generation polymer of this series is the Kraton® G series which are styrene-ethylene-butylene-styrene type (S-EB-S) polymers. Diblock polymers include the ABA type and the SB, styrene-ethylenepropylene (S-EP) and (S-EB). The ABA structure of the Kraton® rubber molecule has polystyrene endblocks and elastomeric midblocks. This series of polymers is sold commercially and indicated as being major compounding ingredients or additives in adhesives, sealants and coatings, asphalt modification for roads and roofing, polymer modification, thermoset modification, and oil modification including use as viscosity index improvers, greases and gels. The Kraton® G rubbers are indicated as being compatible with paraffinic and naphthionic oils and the triblock copolymers are reported as taking up more than 20 times their weight in oil to make a product which can vary in consistency from a "Jello" to a strong elastic rubbery material depending on the grade and concentration of the rubber.
A preferred clear candle body composition of the instant invention is prepared by blending into the hydrocarbon oil the mixture or blend of diblock and triblock or other copolymers in the desired amounts. The amounts of each copolymer and the amount of the mixture contained in the hydrocarbon oil will determine the final form of the gel. Care must be taken to insure the ratio, amount and type of ingredients are correct to yield a clear semi-solid gel. The semi-solid gel is the candle "body."
The gel is formed by blending the polymers and oil and heating them to between about 50° to 90° C to dissolve the polymer blend in the oil. Mixing may be carried out in any conventional manner. On cooling, the gel forms. Fragrance(s) and/or color(s) may be added at any time prior to cooling. Alternatively, a formed gel can be heated to reform the solution, upon which the fragrance(s) and/or color(s) may be added, and the gel allowed to reform on cooling.
The resulting gel is preferably free standing at room temperature (the candle "body") and must be heated to about 200° Fahrenheit (93.3°C), plus or minus 10° before it flows easily. After the fragrance(s) and/or color(s) are mixed into the material it is poured into a container. Typical colors and fragrances which can be used in preferred embodiments are listed in tables 1 and 2.
Table 1
Scent Supplier Scent
Fragrance Lilac 91F/1733 Resources Balsam Pine 91F/1733 Potpourri 92F/2285 Citrus Grove 94F/1517 Pure Peach 94F/1689 Melon Patch 94F/2103
French Mint 308 Chemical Hollyberry 349
Libenn Aroma Black Cherry 11843
Manheimer Pomegranite 801047 Blueberry 830315 Floral Sachet 801021
Noville Wildflower 26445 Sugar Plus 89835 Peppermint AN 100049 Charlie 27950 Pina Colada AN 100050 Magique Noire 28565 Vanilla AN 107067
Table 2
Dye Supplier Color
Bekro Blue 3104 Navy 3464/54 Biege-Rose 3963/37
French Fat Yellow Oil Scarlet Cake Lilac D-270 Oil Orange Cherry Red Navy D-366 Solvent Green
Goldmann Green F2717 Yellow F2825 Blue F2828
Thermocolor 5GS Green Cake
The container for a candle made hereunder can comprise any of a variety of devices which can contain the gel, do not burn, and do not melt. Preferably, a faceted glass container can be used for aesthetic purposes. While it is contemplated that a clear candle made according to the present invention could be provided without a container, due to the gel-like nature of the candle itself, and its potential flowability when heated, it is preferred that such candles include an appropriate container.
A wick is placed in the candle body before the gel firms up. The term "wick" as used herein means any filamentary body which is sufficiently sturdy, which will bum with a flame, and which is capable of drawing up the molten candle material by capillary action. Preferably, the wick can be any properly sized commercially available wick. For example, an appropriately sized Atkins and Pierce 60/40/18 type
wick, saturated with a high molecular weight microcrystalline wax can be used. Also preferably, more than one wick may be used in a single candle according to the present invention.
The blend of copolymers used in the preferred formulation of the clear candle body is a mixture of diblock copolymers and triblock copolymers. Each polymer contains at least two incompatible segments, for example at least one hard and one soft segment. In general in the diblock polymer, segments will be sequential with respect to hard and soft segments. In a triblock polymer, the segment ratio is two hard/ one soft, two hard/one soft, etc. (i.e. a 2-1-2-1 copolymer). The multiblock polymers can contain any combination of hard and soft segments. In the clear candle composition, however, there must always be present at least one diblock and one triblock copolymers, and the combination must also provide both the hard and soft characteristics necessary for the composition. These characteristics are necessary in order to provide the controlled syneresis which is an essential part of the present invention.
The body of the clear candle is thereby preferably provided in a gel form comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of: diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, there being present at least one diblock copolymer and at least one triblock copolymer. While the precise ratio of diblock and triblock copolymers can be varied to provide varying characteristics to the gel, it has been found that both must be present. Preferably, said at least one diblock copolymer and at least one triblock copolymer comprise from about 1 to 99 wt. % of the blend of polymers. Even more preferably, the diblock copolymer forms from about 1 to 3 weight percent of the blend of polymers, while the triblock copolymer forms from about 97 to 99 weight percent of the blend of polymers. It has been found that having a disproportionately large part of the triblock in comparison to the diblock, tends to make the material more gel-like and less prone to crumbling. The diblock or triblock copolymers should also have
copolymers comprising block segments of styrene monomer units and mbber monomer units.
The diameter of the gel candle body is preferably less than 3 inches (7.6 cm) as it has been observed that if the gel candle is larger, the heat of the wick may not melt the entire top of the candle surface. This will leave some gel material around the edges unburned and the candle will bu down the middle, leaving the edges of the container coated with some of the material. This is not preferred for aesthetic reasons, and due to the general wasteful nature of such performance.
Thus, it is apparent that there has been provided a clear candle, in accordance with the present invention, and responding to the aspects and objects as set forth above. While the invention has been described in conjunction with specific embodiments, it is evident that many alternatives, modifications and variations will be apparent to those skilled in the art in light of the foregoing description and examples, and without deviating from the contemplated scope of the present invention. Accordingly, it is intended to embrace all such alternatives, modifications and variations which fall within the spirit and scope of the appended claims.
Claims
1. A candle comprising: at least one wick; a clear body; said wick located in said body; and wherein said body is a clear gel comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, said composition including at least one diblock copolymer and at least one triblock copolymer, with said diblock and triblock polymers comprising segments of styrene monomer units and mbber monomer units.
2. A candle according to claim 1 wherein said at least one diblock copolymer or said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers.
3. A candle according to claim 2 wherein the diblock polymers and triblock copolymers are derived from thermoplastic bbers.
4. A candle according to claim 3 wherein the diblock polymers and triblock polymers contain insoluble portions and soluble portions and are thermoplastic mbbers.
5. A candle according to claim 1 wherein a colorant is added to said clear body.
6. A candle according to claim 1 wherein a fragrance is added to said clear body.
7. A candle according to claim 1, further comprising a container.
8. The candle of claim 7, wherein said body is disposed in said container.
9. The candle of claim 1 , wherein said wick is located adjacent a central axis of said body.
10. A method of using a gel composition as a candle material, said gel composition comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, with the proviso that there be contained in the composition at least one diblock copolymer or at least one triblock copolymer, with said diblock and triblock polymers comprising segments of styrene monomer units and mbber monomer units.
11. The method of claim 10, wherein said at least one diblock copolymer or said at least one triblock copolymer comprise from about 1 to 99 wt. % of said blend of at least two different polymers.
12. The method of claim 11, wherein said gel is clear.
13. The method of claim 10, wherein said at least one triblock copolymer is a copolymer comprising block segments of styrene monomer units and mbber monomer units.
14. The method of claim 12, comprising placing said clear gel in a container and inserting at least one wick in said gel.
15. A candle comprising: at least one wick; a container; a clear body; said wick located in said body, said body being disposed in said container; and wherein said body is a clear gel comprising about 80 to 99 wt. % of a hydrocarbon oil, and about 1 to 20 wt. % of a blend of at least two different polymer members selected from the group consisting of diblock copolymers, triblock copolymers, radial block copolymers and multiblock copolymers, said composition including at least one diblock copolymer and at least one triblock copolymer, with said diblock and triblock polymers comprising segments of styrene monomer units and mbber monomer units.
16. A candle according to claim 15 wherein said at least one diblock copolymer or said at least one triblock copolymer forming 1 to 99 wt. % of said blend of at least two different polymers.
17. A candle according to claim 15 wherein the diblock polymers and triblock copolymers are derived from thermoplastic mbbers.
18. A candle according to claim 16 wherein the diblock polymers and triblock polymers contain insoluble portions and soluble portions and are thermoplastic mbbers.
19. A candle according to claim 15 wherein a colorant is added to said clear body.
20. A candle according to claim 15 wherein a fragrance is added to said clear body.
21. The candle of claim 15, wherein said wick is located adjacent a central axis of said body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU55485/96A AU5548596A (en) | 1995-04-27 | 1996-04-10 | Candle |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US42960695A | 1995-04-27 | 1995-04-27 | |
US08/429,606 | 1995-04-27 | ||
US08/522,837 | 1995-09-01 | ||
US08/522,837 US5578089A (en) | 1995-04-27 | 1995-09-01 | Clear candle |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996034077A1 true WO1996034077A1 (en) | 1996-10-31 |
Family
ID=27028258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/005234 WO1996034077A1 (en) | 1995-04-27 | 1996-04-10 | Candle |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR001737A1 (en) |
AU (1) | AU5548596A (en) |
WO (1) | WO1996034077A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997008282A1 (en) * | 1995-08-29 | 1997-03-06 | Pennzoil Products Company | Transparent gel candles |
US5705175A (en) * | 1996-02-29 | 1998-01-06 | Pennzoil Products Company | Non-aqueous controlled release insect repellent and insecticide gels |
WO1999027042A1 (en) * | 1997-11-20 | 1999-06-03 | SCHÜMANN SASOL GmbH | Candle base material and method for producing a candle base material |
FR2782088A1 (en) * | 1998-08-07 | 2000-02-11 | Xavier Hivet | METHOD OF MAKING LIGHTING CANDLES, AND CANDLES MADE ACCORDING TO THIS METHOD |
FR2790480A1 (en) * | 1999-03-03 | 2000-09-08 | Andre Verstraeten | Ornamental lighting candles made by charging gelatinous particles of candle making material into a glass vessel containing a vertically aligned wick which when burning melts the particles in a defined limited zone round the wick |
DE10138242A1 (en) * | 2001-08-03 | 2003-02-27 | Ehrenburg Marcus Leonid | A completely hydrogenated hydrocarbon resin and fatty acid composition useful for preparation of transparent and stable candles |
US6582484B2 (en) | 1999-03-11 | 2003-06-24 | Reckitt Benckiser (Uk) Limited | Candle composition |
US6585783B1 (en) | 1997-11-20 | 2003-07-01 | SCHÜMANN SASOL GmbH | Candle base material and method for producing a candle base material |
DE10021953B4 (en) * | 1999-08-27 | 2011-10-27 | SCHÜMANN SASOL GmbH | Flammable mass |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3857805A (en) * | 1972-10-27 | 1974-12-31 | Cities Service Oil Co | Hydrocarbon wax composition |
JPS6198780A (en) * | 1984-10-22 | 1986-05-17 | Mitsui Petrochem Ind Ltd | New synthetic wax |
EP0224389A2 (en) * | 1985-11-22 | 1987-06-03 | RAYCHEM CORPORATION (a Delaware corporation) | Styrene-diene block copolymer compositions |
WO1988000603A2 (en) * | 1986-07-18 | 1988-01-28 | Raychem Limited | Gels comprising block copolymers |
US5132355A (en) * | 1990-11-26 | 1992-07-21 | Boris Nahlovsky | Gels of polyethylene block copolymers and liquid hydrocarbons |
US5221534A (en) * | 1989-04-26 | 1993-06-22 | Pennzoil Products Company | Health and beauty aid compositions |
-
1996
- 1996-04-10 AU AU55485/96A patent/AU5548596A/en not_active Abandoned
- 1996-04-10 WO PCT/US1996/005234 patent/WO1996034077A1/en active Application Filing
- 1996-04-26 AR AR33632296A patent/AR001737A1/en unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3857805A (en) * | 1972-10-27 | 1974-12-31 | Cities Service Oil Co | Hydrocarbon wax composition |
JPS6198780A (en) * | 1984-10-22 | 1986-05-17 | Mitsui Petrochem Ind Ltd | New synthetic wax |
EP0224389A2 (en) * | 1985-11-22 | 1987-06-03 | RAYCHEM CORPORATION (a Delaware corporation) | Styrene-diene block copolymer compositions |
WO1988000603A2 (en) * | 1986-07-18 | 1988-01-28 | Raychem Limited | Gels comprising block copolymers |
US5221534A (en) * | 1989-04-26 | 1993-06-22 | Pennzoil Products Company | Health and beauty aid compositions |
US5132355A (en) * | 1990-11-26 | 1992-07-21 | Boris Nahlovsky | Gels of polyethylene block copolymers and liquid hydrocarbons |
Non-Patent Citations (1)
Title |
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PATENT ABSTRACTS OF JAPAN vol. 10, no. 276 (C - 373) 10 September 1986 (1986-09-10) * |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5879694A (en) * | 1995-08-29 | 1999-03-09 | Pennzoil Products Company | Transparent gel candles |
WO1997008282A1 (en) * | 1995-08-29 | 1997-03-06 | Pennzoil Products Company | Transparent gel candles |
US6066329A (en) * | 1995-08-29 | 2000-05-23 | Pennzoil Products Company | Transparent gel candles |
US5705175A (en) * | 1996-02-29 | 1998-01-06 | Pennzoil Products Company | Non-aqueous controlled release insect repellent and insecticide gels |
US5871765A (en) * | 1996-02-29 | 1999-02-16 | Pennzoil Products Company | Non-aqueous controlled release pest and air care gel composition |
US6096102A (en) * | 1997-11-20 | 2000-08-01 | Schumann Sasol Gmbh & Co. Kg | Kerze (candle) |
WO1999027042A1 (en) * | 1997-11-20 | 1999-06-03 | SCHÜMANN SASOL GmbH | Candle base material and method for producing a candle base material |
US6585783B1 (en) | 1997-11-20 | 2003-07-01 | SCHÜMANN SASOL GmbH | Candle base material and method for producing a candle base material |
WO2000008123A1 (en) * | 1998-08-07 | 2000-02-17 | Xavier Hivet | Method for making lighting candles, and candles obtained by said method |
FR2782088A1 (en) * | 1998-08-07 | 2000-02-11 | Xavier Hivet | METHOD OF MAKING LIGHTING CANDLES, AND CANDLES MADE ACCORDING TO THIS METHOD |
FR2790480A1 (en) * | 1999-03-03 | 2000-09-08 | Andre Verstraeten | Ornamental lighting candles made by charging gelatinous particles of candle making material into a glass vessel containing a vertically aligned wick which when burning melts the particles in a defined limited zone round the wick |
US6582484B2 (en) | 1999-03-11 | 2003-06-24 | Reckitt Benckiser (Uk) Limited | Candle composition |
DE10021953B4 (en) * | 1999-08-27 | 2011-10-27 | SCHÜMANN SASOL GmbH | Flammable mass |
DE10138242A1 (en) * | 2001-08-03 | 2003-02-27 | Ehrenburg Marcus Leonid | A completely hydrogenated hydrocarbon resin and fatty acid composition useful for preparation of transparent and stable candles |
Also Published As
Publication number | Publication date |
---|---|
AR001737A1 (en) | 1997-11-26 |
AU5548596A (en) | 1996-11-18 |
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