TW200827435A - Partial acyl glyceride based biowaxes, biocandles prepared therefrom and their preparation methods - Google Patents

Partial acyl glyceride based biowaxes, biocandles prepared therefrom and their preparation methods Download PDF

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TW200827435A
TW200827435A TW95147367A TW95147367A TW200827435A TW 200827435 A TW200827435 A TW 200827435A TW 95147367 A TW95147367 A TW 95147367A TW 95147367 A TW95147367 A TW 95147367A TW 200827435 A TW200827435 A TW 200827435A
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wax
raw
weight
candle
biomass
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TW95147367A
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TWI322180B (en
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Yi-Fa Lee
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Chant Oil Co Ltd
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Abstract

The present invention relates to a biowax comprising a partial acyl glyceride selected from the group consisting of a monoacylglyceride, a diacylglyceride and the combination thereof. The present invention also relates to a biocandle comprising a biowax and a wick, and to a method of producing the same.

Description

200827435 九、發明說明: 【發明所屬之技術領域】 本發明關於一種生質蠟,其包含部份醯基甘油酯 (PAG),本發明亦關於一種由該生質躐形成的生質躐濁, 5 及關於一種製造彼等之方法。 【先前技術】 在市場上已發展出許多種類的蠟燭,習知技術中,蠟 燭係由石蠟及/或天然蠟所製成。某些由習知方法製得的 10 典型躐燭可形成為杯型躐燭(container candles)、祈禱用蠛 燭(votive candles)、柱狀躐燭(pillar candles)、錐形躐燭 (taper candles)、茶躐燭(tea-light candles)及旋風式躐燭 (hurricane candles) 〇 長久以來,已知生質蠟,如蜂蠟(棕櫚酸蜜蠟酯 15 (myricyl palmitate))及錄纖(棕櫚酸蘇鐵 S旨(cetyl palmitate)) 等,可用作為製造蠟燭的天然蠟。近期,隨著石油精煉工 業的發展,石油躐(fossil waxes),如石躐等,亦可作為供 製造蠟燭用的蠟燭蠟之原料。 當今,以石蠟為基質的蠟係作為蠟燭製造的主要原料 20 來源,該石躐係由在石油(fossil oils)精煉後所留下的殘餘 物製得,已發現石蠟可完全地燃燒,惟其燃燒時,通常會 釋出煙霧及產生令人不悅的氣味。 棕櫚硬脂(palm stearin)是來自棕櫊油精製工業的副 產物,每年棕櫚硬脂的產率非常龐大,且其價格遠較石蠟 200827435 便且’已I试使用棕櫚硬脂作為躐燭躐的成分。然而,由 於棕櫚硬脂具有較低熔點的性質,其在蠟燭蠟中的摻合百 分比受到限制且難以控制。而即使棕櫚硬脂可被氫化成較 高熔點的棕櫚硬脂,由其製得的蠟燭反而更為易脆且缺乏 延展性(malleability)。因此,棕櫚硬脂作為蠟燭蠟的成分 之應用仍然受到限制。 為提供具有乾淨燃燒特性的蠟燭,已對具有低石蠟含 夏的躐燭躐進行廣泛之研究,例如美國專利案號 6,503,285、6,645,26卜 6,770,104、6,773,469、6,797,020、 10 15 及6,824,572均揭示以三醯基甘油為底的壤燭蝶,特別是 由各種動物來源及/或植物來源(如植物油源)衍生的蠟燭 蠟0 然而,由以植物油為基質的材料調配得的蠟燭蠟經常 產生各類_。已發現和以錢為基質㈣燭相較下,以 植物油為基質的蠛濁有許多缺點,例如龜裂、形成氣穴㈣ P〇c廿ke〇 ’及例如伴隨黃豆材料的天然產物氣味。此外,該200827435 IX. Description of the Invention: [Technical Field] The present invention relates to a raw material wax comprising a partially mercaptoglyceride (PAG), and the present invention also relates to a biomass turbidity formed by the biomass crucible, 5 and about a method of manufacturing them. [Prior Art] Many kinds of candles have been developed on the market, and in the prior art, wax candles are made of paraffin wax and/or natural wax. Some of the 10 typical candles produced by conventional methods can be formed into cup candles, votive candles, pillar candles, and taper candles. ), tea-light candles and hurricane candles 生 For a long time, raw waxes such as beeswax (myricyl palmitate) and fiber recording (ferric palmitate) have been known. S (cetyl palmitate), etc., can be used as a natural wax for making candles. Recently, with the development of the petroleum refining industry, fossil waxes, such as sarcophagus, can also be used as a raw material for candle wax for making candles. Today, paraffin-based waxes are the source of the main raw material for the manufacture of candles. The sarcophagus is made from residues left after refining of fossil oils. It has been found that paraffin wax can be completely burned, but it burns. At the time, smoke is usually released and an unpleasant smell is produced. Palm stearin is a by-product of the palm oil refining industry. The annual yield of palm stearin is very large, and its price is much higher than that of paraffin 200827435 and 'I have tried palm stearin as a candlestick. ingredient. However, due to the lower melting point properties of palm stearin, its blending percentage in candle wax is limited and difficult to control. Even though palm stearin can be hydrogenated to a higher melting point of palm stearin, the candle made therefrom is more fragile and lacks malleability. Therefore, the application of palm stearin as a component of candle wax is still limited. In order to provide a candle having a clean burning characteristic, extensive research has been conducted on a candle with a low paraffin summer, such as U.S. Patent Nos. 6,503,285, 6,645,26, 6,770,104, 6,773,469, 6,797,020, 10 15 and 6,824,572. A candle based on triterpene glycerol, especially a candle wax derived from various animal sources and/or plant sources (such as vegetable oil sources). However, candle waxes prepared from vegetable oil-based materials often produce class_. It has been found that vegetable oil-based turbidity has many disadvantages, such as cracking, formation of air pockets (4) P〇c廿ke〇', and, for example, the natural product odor accompanying the soybean material, as compared to the money-based (four) candle. In addition, the

以頁豆為基質的徵具有與下述性能A 心士 , -a认 相關的問題:最適當的 火焰大小,付δ均勻燃燒之有效的蠟和燭芯 燃燒時間,產品顏色整合性及/或產品儲存。b 為使產品具有美觀和功能性產品表面=因此 品質,需要開發新穎的以植物油為底的代替蝶。所要求的The Bean-Based Sign has the following problems associated with the following properties: A, the most appropriate flame size, the effective wax and wick burning time for δ uniform burning, product color integration and/or Product storage. b In order to make the product aesthetic and functional, the surface of the product = therefore quality, it is necessary to develop a novel vegetable oil-based replacement butterfly. Required

依此,已有開發代替的蠟材料之需求J 燭時’該代替的料具有乾淨的燃燒田佳=成= 類材料為可生物分解的及衍生自再 貪較佳地,该 生原枓,更佳地,該蠟 20 200827435 濁基質躐材料具有下述物理特性:例如使該材料容易形成 具有令人愉悅的外觀及/或觸感,以及具有理想嗅覺性質 之蠟燭的熔點、硬度及/或延展性等。 再者,京都協定書制定了地球上各方面有關綠色議題 的條約,其目的為“穩定大氣中溫室氣體濃度於可防土危 險之干擾氣候糸統的人為因素(anthropogenic)之含量’,。由 於石油燃料(fossil fuel)來源短缺,且油價持續飆漲,生質 燃料(biomass fuels)在再生能源供給鏈中扮演了極重要角 色。在快速發展的生質柴油(biodiesel)供給鏈中,甘油的 過剩供給變成需解決的迫切問題。 【發明内容】 本發明提供一種以部份醯基甘油酯(PAG)為基質的生 貝蝶’該以PAG為基質的生質躐可消耗大量的甘油,因 此可與該生質柴油供給鏈配合,以解決甘油過量生產問 題。本發明中,消耗甘油以製造以PAG為基質的生質虫鼠 及使用該生質蠟形成環保蠟燭,將有助於地球上碳循環系 的正常發展。最終,其可重導石油能源為極有價值且可行 的農業能源政策。 本發明提供一種以PAG為基質的生質蠟,其適於作 為蠟燭蠟。以火焰長度來論,以PAG為基質的生質織觸 具有與由石蠟製成的商業蠟燭相比擬的燃燒特性,且不會 有令人不悅的氣味。與石蠟相比,該生質蠟具有優異的特 座’包括低黑煙排放及南的添加劑相容性’此使得以Pag 200827435 為基質的生質蠟可有效地代替石蠟。 根據本發明,本發明另提供一種生質蠟燭,其包含生 質蠟及燭芯,其中該生質蠟包含部份醢基甘油酯。又,該 蠟燭亦可由以PAG為基質的生質蠟形成,該生質蠟係含 5 有石蠟及/或硬脂(stearin)作為額外的成分,由其製得的蠟 燭可展現均勻的組成、半透明與細晶粒結晶構造,該蠟燭 通常可乾淨燃燒及釋出極少量的黑煙。由於低黑煙排放性 與生物可分解性之組合,且係由再生原料製造的蠟燭,使 得本發明蠟燭成為特別有利於環保的產品。 1〇 根據本發明,係提供一種製造生質蠟燭之方法,利用 本發明之方法,可形成各種類的生質蠟燭,例如杯型蠟 燭、蠟燭珠粒等。 【實施方式】 15 根據本發明,該生質蠟包含部份醯基甘油酯(PAG), 較佳地,根據本發明之生質蠟包含約20重量%(wt.%)至 100重量%,較佳為30重量%至100重量%的PAG,以生 質犧的總重量為基準。 如本文所使用者,術語“生質蠟”意指由衍生自生質柴 20 油供給鏈的原料所製得的蠟。如本文所使用者,術語“部 分醯基甘油酯”意指一種甘油酯,選自包含單醯基甘油酯 (MAG)、二酿基甘油醋(DAG)及其組合之組群。該部份酿 基甘油酯可藉由甘油分子與一或二種中鏈或長鏈脂肪酸 之酯化反應而製得。如本文所使用者,術語“中鏈脂肪酸” 200827435 意指具有6至10個碳的飽和或不飽和脂肪酸,或其混合 物,又,術語“長鏈脂肪酸”意指具有14至24個碳的飽和 或不飽和脂肪酸,或其混合物。更佳地,該醯基具有C16, C18, C18:l,C18:2之直鏈。根據本發明,部份醢基甘油酯 5 可單獨使用或與三醯基甘油酯及/或其他成分組合使用。 本文中使用的術語“生質蠟燭”意指由生質蠟製得的蠟燭。 根據本發明,生質蠟可進一步包含三醢基甘油酯 (TAG)、硬月旨或石蠟、或其組合物作為額外的成分。於本 發明之一較佳的具體實施例中,生質蠟包含單醯基甘油酯 ίο (MAG)、二醯基甘油酯(DAG)及三醯基甘油酯(TAG)。單 醯基甘油酯較佳用量為約10至75重量%,更佳用量為約 40至70重量%,以生質蠟的重量為基準。二醯基甘油酯 (DAG)較佳用量為約10至50重量%,更佳用量為約10 至35重量%,以生質蠟的重量為基準。選擇性地使用三 15 醯基甘油酯(TAG),其用量可為約5至50重量%,較佳用 量為10至40重量%,以生質蠟的重量為基準。 本發明中,生質蠟可選擇性地包括少量的其他添加 劑,以改質該躐性材料的性質。可併入本發明生質蠛中的 添加劑實例包括:著色劑,香料(例如香精油),抗氧化劑, 20 UV光吸收劑及移動抑制劑,及類似物。較佳地,生質躐 與天然的著色劑摻合,以提供一種均勻單色分布。 生質蠟的熔點為約40至62°c。於一具體實施例中, 該生質蠟具有約0.2至35的碘值。 本發明中,生質蠟可形成所希望的形狀。根據一較佳 200827435 具體實施例’生質躐可形成粉末狀或顆粒。較佳地, 質躐可形成珠粒,其可藉加熱生為溶融態及之後喷 的生質躐而製得,或可藉由購自承德油脂股份 設備製得。根據本發明,生質躐可被成型為具有直= 0.5至1.2毫米的珠粒。 二、 本發明中,生質蠟適於作為製造生質蠟燭的原料。 本發明,提供一種生質蠟燭’其包含生質蠟及燭 心,其中該生質蠟包含部份醯基甘油酯(PAG)。生質蠟燭 基本上為固體、穩定而不脆,通常有點延展性,而益可目 視到的游離油。本發明中,生質蠟燭可藉由熔融工方 法而形成所希望形狀的蠟燭,例如柱狀蠟燭、茶蠟燭等。 15 本發明中,為了能從該以pAG為基質的生質蠟的環 保安全領域巾完整受益,希望使料具有金屬核芯(例如 2或鋅核芯)的濁芯。適合的燭芯材料實例為辮子形棉 芯。燭芯亦可採用用於其他蠟(例如石蠟及/或 二 燭芯。 W心加平 根據本發明,其進一步提供一種製造生質蠟燭之方 t其包含步驟:υ加熱以PAG為基質的生質壤至炫融 狀悲,2)將該熔融的生質蠟引入模具中,其中該模具 含燭芯設置其中,3)將模具中的熔融生質蠟冷卻γ及^ 固化該生質蠟,及之後將該經固化的生質蠟從模具中移 本發明進一步提供一種製造生質蠟燭之方法,其包含 20 200827435 將以PAG為基質的生質蠟加熱至熔融狀態,喷灑冷卻該 生質蠟,以形成〇·5至1.2毫米珠粒,及將該生質蠟珠粒 壓製到模具中,以形成蠟燭。 在生質蠟燭之製程中,重要的是著色劑(若存在)需要 5 被溶解於以PAG為基質的生質蠟中,以防止不溶的顆粒 阻塞燭芯中生質蠟流。通常,受阻塞的生質蠟流會產生不 良的蠟燭燃燒,再者,生質蠟的色澤亦可能影響染色性 能。大部分的香料可被用於生質蠟,以改善所製得的生質 蝶燭性能,如穩定性、反應性、色澤等。 10 根據本發明,所製得的生質蠟燭可乾淨燃燒及釋出極 少量的黑煙。 本發明中,須暸解於說明書及申請專利範圍之所有實 例中代表的成分量、性質等的所有數字係以”約1’字修飾, 及所有份數及百分比意指以重量計,除非另有指定。 15 本發明藉由下述實施例更詳盡地說明,該實施例不意 欲以任何方式限制本發明範圍,雖然設於大範圍的數字範 圍和參數範圍是近似值,但儘可能精確地紀錄在特定的實 施例中的數值。然而,任何數值固有地含有一定偏差,其 係為在各個試驗檢測中必定會產生的標準偏差。 實施例 A. PAG的氣體層析分析Accordingly, there has been a need to develop a replacement wax material when the J candle is used. The substitute material has a clean burning field. The raw material is biodegradable and derived from re-corruption. More preferably, the wax 20 200827435 turbid matrix material has the following physical properties: for example, the material is readily formed to have a pleasant appearance and/or feel, and the melting point, hardness and/or the candle having the desired olfactory properties. Extensibility, etc. Furthermore, the Kyoto Protocol establishes a treaty on all aspects of the world on green issues, with the aim of “stabilizing the concentration of greenhouse gases in the atmosphere against the anthropogenic content of the climate system that is resistant to soil”. There is a shortage of fossil fuel sources, and oil prices continue to soar. Biomass fuels play a very important role in the renewable energy supply chain. In the rapidly growing biodiesel supply chain, glycerol Excess supply has become an urgent problem to be solved. SUMMARY OF THE INVENTION The present invention provides a biosynthesis of a thioglycolate (PAG) based on PAG as a substrate, which can consume a large amount of glycerol, and thus can Cooperating with the biodiesel supply chain to solve the problem of glycerol overproduction. In the present invention, consumption of glycerol to produce PAG-based germplasm pests and use of the biomass wax to form an environmentally friendly candle will contribute to carbon on the earth. The normal development of the circulation system. Finally, its re-directed petroleum energy is an extremely valuable and feasible agricultural energy policy. The present invention provides a PAG for a quality raw wax suitable for use as a candle wax. In terms of flame length, the PAG-based biotextile has a burning characteristic comparable to that of a commercial candle made of paraffin, and there is no such thing as A pleasant smell. Compared with paraffin wax, this raw wax has excellent special features 'including low black smoke emission and south additive compatibility'. This makes the raw wax based on Pag 200827435 effectively replace paraffin. According to the present invention, the present invention further provides a raw material candle comprising a raw material wax and a wick, wherein the raw material wax comprises a partial mercaptoglyceride. Further, the candle may be formed of a PAG-based biomass wax. The raw wax contains 5 paraffin and/or stearin as an additional component, and the candle made therefrom exhibits uniform composition, translucency and fine crystal structure. The candle is usually clean and burnt. The release of a very small amount of black smoke. Due to the combination of low black smoke emission and biodegradability, and the manufacture of candles made from recycled raw materials, the candle of the present invention becomes a particularly environmentally friendly product. provide A method for producing a raw candle, by which the various types of raw candles, such as cup-shaped candles, candle beads, etc., can be formed. [Embodiment] 15 According to the present invention, the raw wax contains a part of the wax. Glyceryl ester (PAG), preferably, the germ wax according to the present invention comprises from about 20% by weight (% by weight) to 100% by weight, preferably from 30% by weight to 100% by weight, of PAG. The total weight is based on the term. As used herein, the term "raw wax" means a wax made from a raw material derived from a supply chain of a biomass 20 oil. As used herein, the term "partial mercaptoglyceride" "A glyceride is selected from the group consisting of monoterpene glycerides (MAG), di-branched glycerol (DAG), and combinations thereof. The partially-branched glyceride can be obtained by esterification of a glycerol molecule with one or two medium or long chain fatty acids. As used herein, the term "medium chain fatty acid" 200827435 means a saturated or unsaturated fatty acid having 6 to 10 carbons, or a mixture thereof, and the term "long-chain fatty acid" means having a saturation of 14 to 24 carbons. Or an unsaturated fatty acid, or a mixture thereof. More preferably, the thiol has a linear chain of C16, C18, C18:1, C18:2. According to the invention, the partially mercaptoglyceride 5 can be used alone or in combination with a trimethyl glyceride and/or other ingredients. The term "biomass candle" as used herein refers to a candle made from raw wax. According to the present invention, the raw material wax may further comprise tridecyl glyceride (TAG), hard moon or paraffin wax, or a combination thereof as an additional component. In a preferred embodiment of the invention, the germ wax comprises monodecyl glyceride ίο (MAG), dimercapto glyceride (DAG) and tridecyl glyceride (TAG). The monodecyl glyceride is preferably used in an amount of from about 10 to 75% by weight, more preferably from about 40 to 70% by weight, based on the weight of the raw wax. The dimercaptoglyceride (DAG) is preferably used in an amount of from about 10 to 50% by weight, more preferably from about 10 to 35% by weight, based on the weight of the raw wax. The tri 15 decyl glyceride (TAG) may optionally be used in an amount of from about 5 to 50% by weight, preferably from 10 to 40% by weight, based on the weight of the raw wax. In the present invention, the raw wax may optionally include a small amount of other additives to modify the properties of the inert material. Examples of additives which may be incorporated into the biomass of the present invention include: colorants, perfumes (e.g., essential oils), antioxidants, 20 UV light absorbers and mobile inhibitors, and the like. Preferably, the biomass 躐 is blended with a natural colorant to provide a uniform monochromatic distribution. The raw wax has a melting point of about 40 to 62 ° C. In one embodiment, the raw wax has an iodine value of from about 0.2 to about 35. In the present invention, the raw wax can form a desired shape. According to a preferred embodiment of the invention, the raw material 躐 can form a powder or granule. Preferably, the enamel can form beads which can be prepared by heating the raw mash and then spraying the mash, or can be obtained by purchasing from Chengde Oils and Fats Co., Ltd. equipment. According to the invention, the green crucible can be shaped to have beads of straight = 0.5 to 1.2 mm. 2. In the present invention, the raw material wax is suitable as a raw material for producing a raw candle. The present invention provides a bio-mass candle comprising a raw wax and a candle, wherein the raw wax comprises a partially mercaptoglyceride (PAG). Biomass candles are essentially solid, stable and not brittle, usually a little malleable, and free of visible oil. In the present invention, the raw candle can be formed into a candle of a desired shape by a melting method, such as a column candle, a tea candle or the like. In the present invention, in order to be able to fully benefit from the environmentally safe safety of the pAG-based biomass wax, it is desirable to have a turbid core of a metal core (e.g., a 2 or zinc core). An example of a suitable wicking material is a braided cotton core. The wick can also be used for other waxes (such as paraffin and / or two wicks. W heart flattening according to the invention, which further provides a method for making a raw candle t comprising the steps of: heating the PAG-based biomass 2) the molten raw wax is introduced into the mold, wherein the mold comprises a wick provided therein, 3) the molten raw wax in the mold is cooled γ and the solid wax is cured, and The solidified wax is then transferred from the mold. The invention further provides a method for producing a green candle comprising 20 200827435. The PAG-based biomass wax is heated to a molten state, and the raw wax is spray-cooled. To form 〇·5 to 1.2 mm beads, and press the raw wax beads into a mold to form a candle. In the process of the raw candle, it is important that the coloring agent, if present, is required to be dissolved in the PAG-based biomass wax to prevent insoluble particles from blocking the flow of the raw wax in the wick. Usually, the blocked wax stream will produce poor candle burning. Furthermore, the color of the raw wax may also affect the dyeing performance. Most of the perfume can be used in the raw wax to improve the performance of the resulting butterfly candle, such as stability, reactivity, color and the like. According to the present invention, the produced raw candle can cleanly burn and release a very small amount of black smoke. In the present invention, it is to be understood that all numbers of ingredients, properties, and the like, which are represented in all examples of the specification and claims, are modified by the word "about 1", and all parts and percentages are by weight unless otherwise The invention is described in more detail by the following examples, which are not intended to limit the scope of the invention in any way, although the numerical ranges and ranges of parameters which are set in the broad range are approximations, Numerical values in a particular embodiment. However, any numerical value inherently contains a certain deviation which is a standard deviation that must be produced in each test. Example A. Gas Chromatographic Analysis of PAG

GC 型號:YOUNGLIN ACME 6000M GC 20 200827435 GC條件:GC Model: YOUNGLIN ACME 6000M GC 20 200827435 GC conditions:

1·管柱:QUADREX熔合矽石毛細管柱; 007-65HT-25W-0.1F, 0.32mmID1. Column: QUADREX fusion meteorite capillary column; 007-65HT-25W-0.1F, 0.32mmID

2. 檢測器:FID 5 10 3. 承載氣體:氮氣 4. 烤箱溫度:2. Detector: FID 5 10 3. Carrier gas: nitrogen 4. Oven temperature:

1) 80°C(維持1分鐘),及以20°C/分鐘之速率到達 240〇C1) 80 ° C (maintained for 1 minute), and reached 240 ° C at a rate of 20 ° C / minute

2) 240°C,及以4°C/分鐘之速率到達360°C 3) 360°C (維持11分鐘)2) 240 ° C, and reach 360 ° C at a rate of 4 ° C / min 3) 360 ° C (maintain 11 minutes)

5. 注入器溫度:280°C5. Injector temperature: 280 ° C

6. 檢測器溫度:360°C6. Detector temperature: 360 ° C

7. 測量範圍·· 6xl03mV 15 樣品之製備: 均勻混合0.2公克的樣品與5毫升的氯仿。 分析條件: 1·樣品量:0.2微升 20 2.分析時間:5 0分鐘 B.用於製備蠟的成分 成份1 :石蠟,供應自台灣蠟品股份有限公司(Taiwan Wax Co·,Ltd·),具有如表1所示物理性質。 200827435 表1 物理性質 試驗方法 數值 Μ·Ρ·,。C ASTM D87 59.8 在25°C針穿刺,毫米 ASTMD1321 15.5 在100°C動力黏度,cps ASTM D445 4.382 油含量,重量% ASTMD721 0.116 色澤 ASTM D156 30 碳分布 ASTM D5442 C20 〜C46 <。26 16.48% 。26-29 23.78% C29-32 23.05% C32-44 36.69% 〉。44 nil η-石蠟 51.05% 成分2 :脂肪酸S1801,供應自Ρ·Τ· MUSIM MAS·,具有 5 如表2所列示物理性質。 表2 物理性質 試驗方法 數值 酸值,毫克KOH/克 ASTM D 1980-87 210.2 皂化值,毫克KOH/克 ASTM D1962-85 211.4 碘值,克碘/100克 ASTM D 1959-97 0.13 -13- 200827435 Μ·Ρ·,。C ASTMD 1982-85 55.4 脂肪酸碳鏈組成,% ASTMD 1983-90 C12+14 0.4 C16 57.67 C18 41.3 其它 0.5 成分3 :脂肪酸1698,供應自P.T. MUSIMMAS.,具有如 表3所列示物理性質。 物理性質 數值 酸值,毫克KOH/克 218.5 皂化值,毫克KOH/克 220 碘值,克碘/100克 0.1 M.P.,。C 62.0 脂肪酸碳鏈組成,% C12+14 0.3 C16 98.6 C18 1.1 其它 0.5 5 表3 成分4 :二種類型的RBD棕櫊硬脂,供應自P.T. MUSIM MAS.,具有如表4所列示物理性質。 -14- 200827435 表4 物理性質 類型1 類型2 游離脂肪酸,% 0.057 0.01 碘值,克埃/100克 20.4 33.3 Μ·Ρ·,。C 56.5 51 脂肪酸碳鏈組成,% C16 72.00 59.8 C18 5.10 3.67 C18:l 16.22 29.7 C18:2 3.67 5.22 成分5 :硬化的油脂F081,由RBD棕橺硬脂(類型2,成 5 分4)在溫度為170至200°C、壓力為3公斤及鎳催化劑 (0.2%)的存在下進行氫化反應4小時而製得者,具有如表 5所列示物理性質。 表5 物理性質 數值 酸值,毫克KOH/克 1.2 皂化值,毫克KOH/克 196.8 埃值,克破/100克 0.4 Μ·Ρ·,。C 57 加納色澤(Color Gardner) 1.3 -15- 200827435 脂肪酸碳鏈組成,% C16 59.8 C18 38.6 成分6 :定義為GMP的部份醯基甘油酯,由200公克的 脂肪酸1698(成分3)與72公克的甘油在250°C反應5小時 而製得者,具有如表6a所列示物理性質,GC分析結果與 數據分別示於圖1與表6b。 10 TAG :三醯基甘油酯 表6a 物理性質 數值 游離脂肪酸,% 1.2 M.P,,。C 56 MAG,% 64.0 DAG,% 25.5 TAG,% 9.3 MAG :單醯基甘油酯 DAG ··二醯基甘油酯 表6b 峰編號 成分 滯留時間(秒) 面積 百分比(%) 1 FFA 8.813 146.88 1.20 2 GMP 14.424 7845.39 63.98 3 GDP 31.754 3132.86 25.54 -16- 200827435 4 GTP 48.118 1137.85 9.28 FFA :游離脂肪酸 GMP :單棕櫚酸甘油酯 GDP :二棕櫚酸甘油酯 GTP :三棕櫚酸甘油酯 成分7 :定義為GMSlv=1.〇的部份醯基甘油g旨,由200公 克的脂肪酸S1801(成分2)與72公克的甘油在250°C反應 5小時而製得者,具有如表7a所列示物理性質,GC分析 結果與數據分別示於圖2與表7b。 10 表7a 物理性質 數值 酸值,毫克KOH/克 0.4 破值,克蛾/100克 0.2 色澤,APHA 140 Μ·Ρ·,。C 56 MAG,% 62.6 DAG,% 28.8 TAG,% 7.6 表7b 峰編號 成分 滯留時間(秒) 面積 百分比(%) 1 G 3.539 519.91 0.65 2 FFA 6.525 233.16 0.29 3 FFA 7.350 46.61 0.06 •17- 200827435 4 單-甘油酯 10.453 48623.36 60.90 5 二-甘油酯 16,861 215.56 0.27 6 二-甘油酯 23.320 24237.86 30.36 7 三-甘油酯 36.047 5964.83 7.47 G :甘油 成分8 :定義為GMSIV=15的部份醯基甘油S旨,由200公克 的含等量F081(成分5)與RBD棕櫚硬脂(類型2,成分4) 之混合物與40公克的甘油在250°C反應8小時而製得者, 具有如表8a所列示物理性質,GC分析結果與數據分別示 於圖3與表8b。 表8a 物理性質 數值 Μ·Ρ·,。C 46 MAG,% 68.35 DAG,% 15.69 TAG,% 11.72 峰編號 成分 滯留時間(秒) 面積 百分比(%) 1 G 2.572 83.89 0.62 2 FFA 6.424 487.76 3.61 3 FFA 7.287 558.61 4.14 -18- 200827435 4 單-甘油酯 9.360 8665.79 64.21 5 二-甘油酯 15.445 10.99 0.08 6 二-甘油酯 19.710 2106.60 15.61 7 三-甘油酯 27.898 6.40 0.05 8 三-甘油酯 29.627 42.31 0.31 9 三-甘油酯 31.626 1532.99 11.36 成分9 :定義為GMSIV=2〇的部份醯基甘油酯,由200 公克的RBD棕櫚硬脂(類型1,成分4)與40公克的甘 油在250°C反應8小時而製得者,具有如表9a所列示 5 物理性質,GC分析結果與數據分別示於圖4與表9b。 表9a 物理性質 數值 色澤 1.4 M.P.,。C 46 MAG,% 49.6 DAG,% 11.1 TAG,% 33.1 表9b 峰編號 成分 滯留時間(秒) 面積 百分比(%) 1 FFA 6.499 989.15 5.25 2 單_甘油酯 9.405 8776.13 46.60 -19- 200827435 3 二·甘油酯 19.948 2471.18 13.12 4 三-甘油酯 27.846 16.10 0.09 5 三-甘油酯 32.311 6582.08 34.95 成分10 :定義為GMSIV=3〇的部份醯基甘油酯,由200公 克的RBD棕櫚硬脂(類型2,來自成分4)與40公克的甘 油在250°C反應8小時而製得者,具有如表10a所列示物 理性質,GC分析結果與數據分別示於圖5與表10b。 表10a 物理性質 數值 Μ·Ρ.,。C 42 MAG,% 66.2 DAG,% 13.4 TAG,% 13.3 表10b 峰編號 成分 滯留時間(秒) 面積 百分比(%) 1 G 2.489 49.89 0.18 2 FFA 6.511 1933.86 6.93 3 單-甘油醋 9.507 18463.30 66.20 4 二-甘油酯 13.502 14.22 0.05 5 二-甘油酯 15.504 20.38 0.07 6 二-甘油酯 20.023 3715.59 13.32 -20- 200827435 7 三-甘油酯 27.924 18.28 0.07 8 三-甘油酯 33.699 3674.74 13.18 驗的杯剞蠟竭的製備(如表li所列示): 將等量用量的不同蠟成分混合及加熱熔融。將熔融的 蝶倒入鋁杯中,鋁杯具有高15毫米X直徑37.5毫米,及 杯子中間配置有23毫米長的辮子狀棉芯。所產生的壤燭 經冷卻及固化,以供燃燒試驗用。 f施例1 $ 13 根據表11所列示的成分及含量製備杯型蠟燭。 5·^燃燒試驗 由以部份醯基甘油酯(PA G)為基質的生質蠟製得的生 質蠟燭,其燃燒性能藉由下述步驟進行: 1·將各個含有不同用量的蠟成分之杯型蠟燭編號及秤重; 2·將杯型蠟燭放在實驗台上,以1〇〇毫米間距相隔放置; 3·將石膏板放在桌台上方75毫米高處,以觀察在燃燒時 由蠟燭釋出的黑煙; 4. 點燃杯型蝶燭及開始料;#各邮周_有—圈蝶液 ,(約5至6分鐘)’儘快地測量各杯型蠟燭的火焰高度; 5. 母隔1小時再測量一次火焰高度; 6. 在60分鐘後,測量各杯型壞濁在内焰最高點的火焰溫 200827435 7·在它們之任一者燃燒完全後,全部熄火,將各杯型蠟燭 秤重;之後計算各杯型蠟濁的燃燒速率。 杯型蠟燭的燃燒試驗結果如表11所示。 表11 實施例編號 1 2 3 4 5 6 7 8 9 幽歹) 10 11 12 13 成分1 :石蠟(重量,克) 3.91 4.94 5.23 7.78 7.49 成分2:S1801(重量,克) 3.91 4.94 5.49 7.99 7.49 成分5 : F081(重量,克) 3.91 5.23 5.49 7.78 成分6: GMP(重量,克) 21.59 成分7:GMSrv^重量,克) 3.91 4.94 5.23 5.49 7,99 7.78 7.78 15.32 成分8:avlS^15(重量,克) 23.26 成分9:C^IW重量,克) 22.87 成分10:QviW重量,克) 22.04 性質 MP(°〇 50.5 52 52 51.5 52 53 57.5 54 52 46 46 42 52 初重(克) 15.64 14.82 15.69 16.47 15.98 15.56 15.56 15.32 14.98 23.26 22.87 22.04 21.59 殘重(克),132分鐘後 4.77 3.10 3.64 6.76 7.37 5.60 2.78 3.62 3.88 14.24 14.00 15.11 10,60 燃燒速率(克/小時) 4.94 5.32 5.48 4.42 3.91 4.53 5.80 5.32 5.04 4.10 4,03 3.15 5.00 火焰溫度(°C) 731 768 757 711 729 777 839 881 806 835 740 668 820 火焰高度(毫米),6分鐘後 26 27 25 23 24 24 27 22 33 15 25 20 25 火焰高度(毫米),70分鐘後 26 26 26 22 15 25 30 22 28 18 18 10 18 火焰高度(毫米),132分鐘後 21 24 30 20 15 23 23 21 27 15 17 6 24 如表11所示,由本發明生質蠟製成的生質蠟燭,搭配平 -22- 200827435 衡量用量的石蠟及/或硬脂一起使用,由目視外觀顯示, 其展現優異的蠟流經燭芯的特性,同時本發明的生質蠟燭 顯示穩定燃燒速率及良好的外觀(例如色澤,香氣及清澈 度),及在燃燒時亦僅釋出低量的黑煙及有良好的氣味。 5 述於本文之本發明的具體實施例係為較佳的,在不悖 離本發明的精神與範圍下可進行各種改質及改良,本發明 的範圍由隨附的申請專利範圍指明,及所有落在等同物的 意義與範圍的改變均涵蓋其中。 10 【圖式簡單說明】 圖1顯示實施例13之GMP的氣體層析分析結果。 圖2顯示實施例8的部份醯基甘油酯(定義為GMSIV=1.〇) 的氣體層析分析結果。 圖3顯示實施例10之部份醯基甘油酯(定義為GMSiv=15) 15 的氣體層析分析結果。 圖4顯示實施例11的部份醯基甘油酯(定義為GMSiv=20) 的氣體層析分析結果。 圖5顯示實施例12的部份醯基甘油酯(定義為GMSiv=30) 的氣體層析分析結果。 20 【主要元件符號說明】 (無) -23-7. Measurement range·· 6xl03mV 15 Preparation of sample: Mix 0.2 g sample and 5 ml chloroform uniformly. Analytical conditions: 1. Sample size: 0.2 μl 20 2. Analysis time: 50 minutes B. Ingredients used to prepare waxes Component 1: Paraffin wax, supplied from Taiwan Wax Co., Ltd. , having the physical properties as shown in Table 1. 200827435 Table 1 Physical properties Test method Value Μ·Ρ·,. C ASTM D87 59.8 Needle puncture at 25 ° C, mm ASTMD1321 15.5 Dynamic viscosity at 100 ° C, cps ASTM D445 4.382 Oil content, weight % ASTMD721 0.116 Color ASTM D156 30 Carbon distribution ASTM D5442 C20 ~ C46 <. 26 16.48%. 26-29 23.78% C29-32 23.05% C32-44 36.69% 〉. 44 nil η-paraffin 51.05% Ingredient 2: Fatty acid S1801, supplied from Ρ·Τ· MUSIM MAS·, having 5 physical properties as listed in Table 2. Table 2 Physical properties Test method Numerical acid value, mg KOH / gram ASTM D 1980-87 210.2 Saponification value, mg KOH / gram ASTM D1962-85 211.4 Iodine value, gram iodine / 100 g ASTM D 1959-97 0.13 -13- 200827435 Μ·Ρ·,. C ASTMD 1982-85 55.4 Fatty acid carbon chain composition, % ASTMD 1983-90 C12+14 0.4 C16 57.67 C18 41.3 Other 0.5 Ingredient 3: Fatty acid 1698, supplied from P.T. MUSIMMAS., having the physical properties as listed in Table 3. Physical Properties Value Acid value, mg KOH/g 218.5 Saponification value, mg KOH/g 220 Iodine value, gram iodine/100 g 0.1 M.P.,. C 62.0 Fatty acid carbon chain composition, % C12+14 0.3 C16 98.6 C18 1.1 Other 0.5 5 Table 3 Ingredient 4: Two types of RBD palm 櫊 stearin, supplied from PT MUSIM MAS., with physical properties as listed in Table 4 . -14- 200827435 Table 4 Physical Properties Type 1 Type 2 Free fatty acids, % 0.057 0.01 Iodine value, gram/100 g 20.4 33.3 Μ·Ρ·,. C 56.5 51 Fatty acid carbon chain composition, % C16 72.00 59.8 C18 5.10 3.67 C18:l 16.22 29.7 C18:2 3.67 5.22 Ingredient 5: Hardened fat F081, from RBD brown stearin (type 2, into 5 points 4) at temperature The hydrogenation reaction was carried out for 4 hours in the presence of 170 to 200 ° C, a pressure of 3 kg, and a nickel catalyst (0.2%), and had the physical properties as listed in Table 5. Table 5 Physical Properties Value Acid value, mg KOH/g 1.2 Saponification value, mg KOH/g 196.8 angstrom value, gram break/100 g 0.4 Μ·Ρ·,. C 57 Color Gardner 1.3 -15- 200827435 Fatty acid carbon chain composition, % C16 59.8 C18 38.6 Ingredient 6: Partially defined as GMP, mercaptoglyceride, from 200 grams of fatty acid 1698 (ingredient 3) and 72 grams The glycerol was prepared by reacting at 250 ° C for 5 hours, and had the physical properties as shown in Table 6a. The GC analysis results and data are shown in Figures 1 and 6b, respectively. 10 TAG: tridecyl glyceride Table 6a Physical properties Value Free fatty acid, % 1.2 M.P,,. C 56 MAG,% 64.0 DAG,% 25.5 TAG,% 9.3 MAG : monodecyl glyceride DAG ··dimercaptoglyceride Table 6b Peak number component retention time (seconds) Area percentage (%) 1 FFA 8.813 146.88 1.20 2 GMP 14.424 7845.39 63.98 3 GDP 31.754 3132.86 25.54 -16- 200827435 4 GTP 48.118 1137.85 9.28 FFA: free fatty acid GMP: monopalmitate GDP: dipalmitate GTP: tripalmitin component 7: defined as GMSlv= 1. A part of hydrazine glycerol, prepared by reacting 200 g of fatty acid S1801 (ingredient 2) with 72 g of glycerol at 250 ° C for 5 hours, having physical properties as shown in Table 7a, GC The analysis results and data are shown in Figure 2 and Table 7b, respectively. 10 Table 7a Physical Properties Value Acid value, mg KOH / gram 0.4 breaking value, gram moth / 100 g 0.2 color, APHA 140 Μ · Ρ ·,. C 56 MAG,% 62.6 DAG,% 28.8 TAG,% 7.6 Table 7b Peak number component retention time (seconds) Area percentage (%) 1 G 3.539 519.91 0.65 2 FFA 6.525 233.16 0.29 3 FFA 7.350 46.61 0.06 •17- 200827435 4 Single - glyceride 10.453 48623.36 60.90 5 di-glyceride 16,861 215.56 0.27 6 di-glyceride 23.320 24237.86 30.36 7 tri-glyceride 36.047 5964.83 7.47 G: glycerin component 8: defined as GMSIV=15 partial thioglycol S Prepared by reacting 200 grams of a mixture of equal amounts of F081 (ingredient 5) with RBD palm stearin (type 2, ingredient 4) with 40 grams of glycerol at 250 ° C for 8 hours, as listed in Table 8a The physical properties, GC analysis results and data are shown in Figure 3 and Table 8b, respectively. Table 8a Physical properties Values Μ·Ρ·,. C 46 MAG,% 68.35 DAG,% 15.69 TAG,% 11.72 Peak number Component retention time (seconds) Area percentage (%) 1 G 2.572 83.89 0.62 2 FFA 6.424 487.76 3.61 3 FFA 7.287 558.61 4.14 -18- 200827435 4 Mono-glycerol Ester 9.360 8665.79 64.21 5 Di-glyceride 15.445 10.99 0.08 6 Di-glyceride 19.710 2106.60 15.61 7 Tri-glyceride 27.898 6.40 0.05 8 Tri-glyceride 29.627 42.31 0.31 9 Tri-glyceride 31.626 1532.99 11.36 Ingredient 9: Defined as GMSIV = 2 〇 part of decyl glyceride, prepared by reacting 200 grams of RBD palm stearin (type 1, ingredient 4) with 40 grams of glycerol at 250 ° C for 8 hours, as shown in Table 9a 5 Physical properties, GC analysis results and data are shown in Figure 4 and Table 9b, respectively. Table 9a Physical properties Numerical Colour 1.4 M.P.,. C 46 MAG,% 49.6 DAG,% 11.1 TAG,% 33.1 Table 9b Peak number component retention time (seconds) Area percentage (%) 1 FFA 6.499 989.15 5.25 2 Mono-glyceride 9.405 8776.13 46.60 -19- 200827435 3 Diglycerol Ester 19.948 2471.18 13.12 4 Tri-glyceride 27.846 16.10 0.09 5 Tri-glyceride 32.311 6582.08 34.95 Ingredient 10: Partially defined as GMSIV=3〇 part of mercaptoglyceride, from 200 g of RBD palm stearin (type 2, from Ingredient 4) was prepared by reacting 40 g of glycerol at 250 ° C for 8 hours, having physical properties as shown in Table 10a, and GC analysis results and data are shown in Figures 5 and 10b, respectively. Table 10a Physical properties Values Μ·Ρ.,. C 42 MAG,% 66.2 DAG,% 13.4 TAG,% 13.3 Table 10b Peak number Component retention time (seconds) Area percentage (%) 1 G 2.489 49.89 0.18 2 FFA 6.511 1933.86 6.93 3 Mono-glycerol 9.507 18463.30 66.20 4 II- Glycerides 13.502 14.22 0.05 5 Di-glycerides 15.504 20.38 0.07 6 Di-glycerides 20.023 3715.59 13.32 -20- 200827435 7 Tri-glycerides 27.924 18.28 0.07 8 Tri-glycerides 33.699 3674.74 13.18 Preparation of cups and waxes As listed in Table li): Mix equal amounts of different wax components and heat and melt. The molten butterfly was poured into an aluminum cup having a height of 15 mm X and a diameter of 37.5 mm, and a 23 mm long braided cotton core disposed in the middle of the cup. The resulting candle is cooled and solidified for combustion testing. f Example 1 $ 13 Prepare a cup candle according to the ingredients and contents listed in Table 11. 5·^Combustion test The biomass candle made from the biomass wax with partial mercaptoglyceride (PA G) as the matrix, its combustion performance is carried out by the following steps: 1. Each wax component containing different amounts Cup type candle number and weighing; 2. Place the cup type candle on the test bench and place it at intervals of 1 mm; 3. Place the gypsum board at a height of 75 mm above the table to observe when burning Black smoke released by the candle; 4. Light the cup-shaped butterfly candle and start the material; #邮邮周_有-圈蝶液, (about 5 to 6 minutes) 'Measure the flame height of each type of candle as soon as possible; 5 The flame height is measured once every 1 hour; 6. After 60 minutes, the flame temperature of each cup type is measured at the highest point of the inner flame. 200827435 7. After all of them are completely burned, all will be extinguished, and each will be fired. The cup type candle is weighed; then the burning rate of each cup type wax is calculated. The results of the burning test of the cup-shaped candle are shown in Table 11. Table 11 Example No. 1 2 3 4 5 6 7 8 9 歹) 10 11 12 13 Ingredient 1: Paraffin (weight, gram) 3.91 4.94 5.23 7.78 7.49 Ingredient 2: S1801 (weight, gram) 3.91 4.94 5.49 7.99 7.49 Ingredients 5 : F081 (weight, gram) 3.91 5.23 5.49 7.78 Ingredient 6: GMP (weight, gram) 21.59 Ingredient 7: GMSrv^weight, g) 3.91 4.94 5.23 5.49 7,99 7.78 7.78 15.32 Ingredient 8: avlS^15 (weight, g) 23.26 Ingredient 9: C^IW weight, g) 22.87 Ingredient 10: QviW weight, g) 22.04 Properties MP (°〇50.5 52 52 51.5 52 53 57.5 54 52 46 46 42 52 Initial weight (g) 15.64 14.82 15.69 16.47 15.98 15.56 15.56 15.32 14.98 23.26 22.87 22.04 21.59 Residual weight (g), after 132 minutes 4.77 3.10 3.64 6.76 7.37 5.60 2.78 3.62 3.88 14.24 14.00 15.11 10,60 Burning rate (g/hr) 4.94 5.32 5.48 4.42 3.91 4.53 5.80 5.32 5.04 4.10 4 ,03 3.15 5.00 Flame temperature (°C) 731 768 757 711 729 777 839 881 806 835 740 668 820 Flame height (mm), after 6 minutes 26 27 25 23 24 24 27 2 2 33 15 25 20 25 Flame height (mm), after 70 minutes 26 26 26 22 15 25 30 22 28 18 18 10 18 Flame height (mm), after 132 minutes 21 24 30 20 15 23 23 21 27 15 17 6 24 As shown in Table 11, the raw candle made of the raw material wax of the present invention is used together with the paraffin wax and/or hard fat measured by Ping-22-200827435, and is visually displayed, which exhibits an excellent wax flow through the wick. The characteristics of the present invention also show that the raw candle of the present invention exhibits a stable burning rate and a good appearance (e.g., color, aroma and clarity), and also releases only a low amount of black smoke and a good odor when burned. 5 The present invention is described in detail herein, and various modifications and improvements can be made without departing from the spirit and scope of the invention. All changes in the meaning and scope of the equivalents are covered. 10 [Simple Description of the Drawing] Fig. 1 shows the results of gas chromatography analysis of GMP of Example 13. Figure 2 shows the results of gas chromatographic analysis of a part of mercaptoglyceride of Example 8 (defined as GMSIV = 1.5). Figure 3 shows the results of gas chromatographic analysis of a portion of mercaptoglyceride (defined as GMSiv = 15) 15 of Example 10. Figure 4 shows the results of gas chromatographic analysis of a portion of the mercaptoglyceride of Example 11 (defined as GMSiv = 20). Figure 5 shows the results of gas chromatographic analysis of a portion of the mercaptoglyceride of Example 12 (defined as GMSiv = 30). 20 [Description of main component symbols] (none) -23-

Claims (1)

200827435 200827435 15 20 2· 3· 4· 5· 6· 申請專利範圍·· L 一種生質蠟(bi〇wax),包含部分醯基甘油酯,其選 自包含單醯基甘油酯及二醯基甘油酯及其組合^組 群。 、 根據申請專利範圍第丨項之生㈣,其中該部份酿 基甘油酯以20重量%至1〇0重量%的用量存在,以 生質蠟的總重量為基礎。 ,據申請專利範圍第】項之生_,其中該部份酿 基甘油醋以30重量%至100重量%的用 生質蠟的總重量為基準。 ^據申請專利範圍第1項之生質蝶,其另包含三醯 基甘油酯。 =申請專利範圍第4項之生㈣,其 為約10至75重量%,及二酸基甘油醋 量為約5 δ 醯基甘油酯的用 柜攄以生質蠟的重量為基準。 圍第5項之生質蟻,其中該三醯基 用量為W。至4。重量%,以生議重 根據申請專利範圍第丨 ί ί f含著色劑、抗氧化劑或香:油項之生貝壤’ 經==範毫=生㈣’其形成具有直 根據申請專利範圍第1至6項中任-項之生質蠛, •24- 9· 200827435 其具有熔點為約40至62°C。 I 〇·根據申凊專利範圍第1至6項中任一項之生質壤, 其具有蛾值為約0.2至35。 II · 一種生為蝶燭,係包含申請專利範圍第1至6項中 5 任一項的生質蠟,及燭芯。 12· —種製造生質蝶燭(bi〇can(jie)之方法,包含下列步 驟: 1) 將以PAG為基質的生質蠟加熱至熔融狀態; 2) 將該熔融的生質蠟引入模具中,其中該模具中包 ίο 含燭芯設置其中; 3) 將模具中的熔融生質蠟冷卻,及 4) 固化該生質蠟,及之後將該經固化的生質蠟從模 具中移除; ' 其申生質蠟包含部分醯基甘油酯,其選自包含單醯 15 基甘/由S曰、一驢基甘油酯及其組合之組群。 13· —種製造生質蝶燭之方法,包含下列步驟·· 1) 將以PAG為基質的生質蠟加熱至熔融狀態; 2) 喷灑冷卻該熔融的生質蠟,以形成〇·5至12毫米 珠粒,及 10 3)將该生負蟻珠粒壓製到模具中,以形成蝶燭。 -25-200827435 200827435 15 20 2· 3· 4· 5· 6· Patent Application Scope·· L A bio-based wax (bi〇wax) containing a partially mercaptoglyceride selected from the group consisting of monodecyl glycerides and diterpenoids Glycerides and combinations thereof. According to the fourth paragraph of the patent application, the portion of the glyceryl ester is present in an amount of from 20% by weight to 1.0% by weight based on the total weight of the raw wax. According to the patent application scope, the glycerin vinegar is based on the total weight of the raw wax of 30% by weight to 100% by weight. According to claim 1, the raw butterfly of the patent scope includes the trimethyl glyceride. = Application No. 4 of the patent scope (4), which is about 10 to 75% by weight, and the amount of the diacid-based glycerin is about 5 δ decyl glyceride, based on the weight of the raw wax. The ant colony of the fifth item, wherein the amount of the triterpene group is W. To 4. % by weight, in terms of the weight of the application, according to the scope of the patent application 含ί ί f containing colorants, antioxidants or fragrant: the oil of the raw shell soil 'pass == Fan milli = raw (four)' its formation has a straight line according to the scope of the patent application To 6 of the items - the quality of the product, • 24-9·200827435 which has a melting point of about 40 to 62 ° C. I. The raw soil of any one of claims 1 to 6 which has a moth value of about 0.2 to 35. II. A raw butterfly candle comprising the raw material wax of any one of the claims 1 to 6 and the wick. 12. A method for producing a biomass butterfly (bi), comprising the steps of: 1) heating a PAG-based biomass wax to a molten state; 2) introducing the molten biomass wax into a mold Wherein the mold contains a wick containing a wick therein; 3) cooling the molten raw wax in the mold, and 4) curing the raw wax, and then removing the cured raw wax from the mold ; The stilbene wax thereof comprises a partially mercaptoglyceride selected from the group consisting of monoterpene 15 glycol/S曰, monodecyl glyceride and combinations thereof. 13· A method for producing a raw butterfly candle, comprising the following steps: 1) heating the PAG-based biomass wax to a molten state; 2) spraying and cooling the molten biomass wax to form a 〇·5 Up to 12 mm beads, and 10 3) The raw negative ant beads are pressed into a mold to form a butterfly candle. -25-
TW95147367A 2006-12-18 2006-12-18 Partial acyl glyceride based biowaxes and candles prepared therefrom TWI322180B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101705157B (en) * 2009-11-17 2012-06-06 宁波旷世智源工艺设计股份有限公司 Aromatic candle with skin care effect and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101705157B (en) * 2009-11-17 2012-06-06 宁波旷世智源工艺设计股份有限公司 Aromatic candle with skin care effect and preparation method thereof

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