WO2004099352A2 - Additives and methods for reducing odor - Google Patents
Additives and methods for reducing odor Download PDFInfo
- Publication number
- WO2004099352A2 WO2004099352A2 PCT/US2004/013704 US2004013704W WO2004099352A2 WO 2004099352 A2 WO2004099352 A2 WO 2004099352A2 US 2004013704 W US2004013704 W US 2004013704W WO 2004099352 A2 WO2004099352 A2 WO 2004099352A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oil
- odor reducing
- reducing additive
- odor
- mixture
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/34—Fragrance or deodorizing properties
Definitions
- This invention relates to additives and methods for reducing odor in oil based media, and to oil based media mixtures having reduced odor.
- Asphalt representing one example of oil based media
- asphalt is an important material for building and repairing roads. It is also used in applications such as roofing and weather sealing.
- hot mix asphalt produces volatile materials such as hydrocarbons, sulfides, and mercaptans, which can have strong, persistent and potentially harmful odors.
- the odors can cause discomfort to persons working with the hot asphalt, to residents living near areas where asphalt is manufactured or paved and generally to persons who come within close range of the hot asphalt.
- Traditional odor treating compositions act as deodorizers or masking agents, essentially overwhelming the undesired odor with another odor. Such techniques, however, are poor at masking strong odors.
- the invention provides a method for reducing odor in oil based media, said method comprising mixing an odor reducing amount of an odor reducing additive with the oil based medium, wherein the odor reducing additive is an essential oil, an essential oil component, or mixtures thereof.
- the invention also provides mixtures having reduced odor comprising: an oil based medium; and an odor reducing additive, wherein the odor reducing additive is an essential oil, an essential oil component, or mixtures thereof.
- FIG. 1 is a GC trace of a blank sample showing a volatile substance given off by septa when heated to 151°C.
- FIGS. 2, and 3 are GC traces of the headspace above an asphalt sample.
- FIG. 4 is a GC trace of the headspace above an asphalt sample containing an odor reducing additive.
- FIG. 5 is a GC trace of the headspace above an asphalt sample containing an odor reducing additive.
- FIGS. 6 is a GC trace of the headspace above an asphalt sample.
- FIG. 7 is a GC trace of the headspace above an asphalt sample containing an odor reducing additive.
- FIG. 8 is a GC trace of the headspace above an asphalt sample containing an odor reducing additive.
- the invention provides odor reducing additives and methods for reducing odors in oil based media.
- the odor reducing additive is one or more essential oils or essential oil components.
- essential oils is meant natural extracts of various parts of aromatic plants and trees.
- essential oil components is meant any of the components which make up an essential oil. Examples of such components include, but are not limited to, te ⁇ enes, alcohols, aldehydes, aromatics, phenolics, esters, te ⁇ ene derivatives, non te ⁇ ene essential oil components, and te ⁇ ene reactants.
- Preferred odor reducing additives are te ⁇ enes, or essential oils containing te ⁇ enes as components.
- te ⁇ enes encompasses all variations of te ⁇ enes and their derivatives, including hydrocarbon te ⁇ enes, unsaturated te ⁇ enes, oxygen containing te ⁇ enes (te ⁇ enoids) such as alcohols, aldehydes, ketones, esters, acetates, ketals and oxides, as well as te ⁇ enes of various chain lengths, including monote ⁇ enes, sesquite ⁇ enes, dite ⁇ enes, trite ⁇ enes, and tetrate ⁇ enes.
- te ⁇ enes occur naturally in plants as constituents of essential oils or they may form from the process of extraction (such as steam distillation, water distillation, hydro distillation or solvent extraction) of the oil from the plant material. Te ⁇ enes may be formed by further processes such as the result of oxygen or hydroxyl addition via acid hydrolysis or by air oxidation or via synthetic or natural reagents.
- the te ⁇ enes can be isolated from the oils in order to intensify the te ⁇ enes' effectiveness, or essential oils may be used in their whole, especially where the oils naturally contain high concentrations of te ⁇ enes.
- oils suitable for use in the invention include: ajowan, angelica root, angelica root himalayan, angelica seed, aniseed china star, anise seed, aniseed, armoise, artemisia, asafoetida, backhousia anisata, lemon myrtle oil certified, basil, basil intensn, basil sweet linalool, basil methyl chavicol, bay west indies, bergamot calabrian, bergamot ivory coast, bergamot mint, bergamot non-phototoxic, borneo camphor, buchu, cabreuva, cajeput ambon, camphor white oil, cananga, caraway, cardamon, carrot seed, carrot seed European, cassia, cedarwood atlas, cedarwood Chinese, cedarwood himalayan, cedar leaf, cedarwood texas, cedarwood Virginian, celery seed, chamomile german extra blue, chamomile wild moroccan, chamomile matric
- the odor reducing additives of the invention reduce odor by interacting with odor causing compounds in oil based media.
- preferred additives are those that contain components capable of interacting with odor causing substances.
- Such components include for example: unsaturated te ⁇ enes; phenolics such as eugenol (an isolate from clove oil; this is not a te ⁇ ene but is still an essential oil component) which can react for instance with acids and base derived odors; primary, secondary, and tertiary alcohols such as linalool, citronellol, te ⁇ ineol and especially tertiary alcohols, which can form odor reactive carbocations; oxides, such as 1,4 cineole, 1,8 cineole, and linalool oxide; ketones such as camphor, a common constituent of essential oils like Rosemary and Sage oil or it maybe manufactured as a derivative of tu ⁇ entine oil.
- Odor reducing additives can also be selected for a particular application based on the ability of the components in the additive to dissolve or bind odorous compounds. Since, as is well known, like dissolves like, essential oil components can be selected according to their similarity in structure to the odor to be reduced or eliminated. For example, if the odor is a hydrocarbon, then a hydrocarbon te ⁇ ene, such as ⁇ -pinene, ⁇ -pinene, ⁇ -3 carene, or dipentene, or mixtures thereof is preferred. If the odor is styrene, then te ⁇ enes such as p-cymene or p- cymenene are preferred for treating this odor.
- essential oil components that reduce odors such as ammonia, sulfur and mercaptans can be readily selected.
- a broad spectrum of odors is to be treated, a broad-spectrum mix of essential oils and/or essential oil components can be used, thus combining the reactivity of a number of components.
- One preferred odor reducing additive is a broad spectrum mixture of components and/or essential oils and includes:
- Another preferred odor reducing additive includes:
- Another preferred odor reducing additive that is especially useful for reducing or eliminating hydrocarbon odors is one or more te ⁇ enes, selected from d-limonene,
- Another preferred odor reducing additive comprises as primary constituents: (+) limonene, pine extract and pine white oil, pinus sylvestris oil, anise seed oil, and clove bud oil.
- the additive may contain additional miscellaneous oils including aniseed oil, camphor white oil, cedarwood atlas oil, cedarwood texas oil, cedarwood Virginia oil, lavandin absolute, lime distilled oil, olibanum extract, rosemary oil, sandlewood west indian oil, tocopherol alpha, and vanilla.
- these components are present at a volume ratio of about 35-45 % of (+) limonene, about 25- 35 % of pine extract and pine white oil, about 1-5 % pinus sylvestris oil, about 3-8 % anise seed oil, about 3-8 % clove bud oil and about 20-25 % miscellaneous oils.
- This additive is preferred for reducing odor where the oil based medium is liquid asphalt cement.
- the amount of odor reducing additive that is added to oil based media will depend on several factors including whether isolated essential oil components or essential oils are used, the concentration of components in the essential oils, the quantity of volatiles in the oil based media that cause the odor, and the cost of the particular component(s) or essential oil(s). As a general guideline, it is preferred that about 0.0001 to about 10 %, more preferably about 0.0003 % to about 3 %, by volume, of odor reducing additive is used, relative to the volume amount of oil based media.
- the odor reducing additive can be added directly to an odor producing oil based medium, or it can be diluted with a carrier oil. Dilution with a carrier oil is especially useful where only a very small amount of additive is required to reduce odor, thereby facilitating handling of the additive. Dilution with a carrier oil can also help dissolve or disperse the additive in the oil based medium.
- Suitable carrier oils include, for instance, mineral oil, vegetable oil, fatty acid alkyl esters, or mixtures thereof.
- a preferred carrier oil is fatty acid alkyl esters or mixtures of fatty acid alkyl esters.
- the fatty component of the fatty acid ester is linear or branched C 8 - C 20 alkyl.
- the alkyl component of the fatty acid ester is linear or branched C ⁇ -C 6 alkyl.
- Preferred carrier oils includes fatty acid methyl ester(s) and fatty acid ethyl esters.
- Preferred oils also include methyl and ethyl esters of palm, coconut, canola, peanut, sunflower, and safflower oils.
- Another preferred carrier oil is SOYGOLD® 1000, which contains alkyl C ⁇ 6 -C ⁇ 8 methyl esters, and is a methyl ester of soybean oil. SOYGOLD® 1000 is available from AG Environmental Products L.L.C., Lenexa, Kansas.
- the ratio of odor reducing additive to carrier oil is about 1-50 % by volume of odor reducing additive and about 50-99 % by volume of carrier oil.
- Oil based media with which the odor reducing additives of the invention can be used include all oil based media that produce odors.
- examples of such media include, but are not limited to, wax based products such as candles, resins, fuel oil, waste oil fuel oil, synthetic lubricants, rubber, liquid asphalt cement, and hot mix asphalt.
- Preferred oil based media include wax based products, liquid asphalt cement, hot mix asphalt and waste oil fuel oil.
- the odor reducing additives of the invention When added to wax based products, such as candles, the odor reducing additives of the invention function to reduce or eliminate odors in the area surrounding the location where the candle is being burned. Thus, burning of a candle containing the odor reducing additive of the invention reduces odors in the surroundings of the candle.
- the odor reducing additive is diluted with carrier oil prior to addition of the additive to the wax.
- the ratio is about 35 to about 45 volume % of additive to about 55-65 % by weight of carrier oil.
- the total amount of odor reducing additive and carrier oil that is mixed with the wax is about 10 to about 15 % based on the volume of the wax.
- hot mix asphalt contains at least two major components; liquid asphalt cement ("liquid AC," also known as “binder”) and aggregates.
- liquid AC functions to coat and bind together the aggregate particles.
- the aggregates provide stability and strength to the asphalt mixture.
- Aggregates can be, for example, crushed rock, fillers, gravel, stone, quarry gravel and recycled paving material.
- the odor reducing additive used with hot mix asphalt is first diluted with a carrier oil, such as fatty acid alkyl esters, prior to addition to the asphalt.
- a carrier oil such as fatty acid alkyl esters
- the ratio of additive to carrier oil is about 1-5 % by volume of additive to about 95-99 % by volume of carrier oil.
- the diluted additive is mixed with the liquid AC prior to mixing of the liquid AC with the aggregates.
- the diluted additive is mixed with the liquid AC during or after refinement of the liquid AC from crude oil, or at a liquid AC terminal, or at a hotmix asphalt plant prior to mixing of the liquid AC with aggregates.
- the ratio of the total amount of odor reducing additive and carrier oil that is mixed with the liquid AC is about 0.001 to about 0.05 % of additive and carrier oil to about 99.999-99.95 % by volume of liquid AC. More preferably, the ratio is about 0.007-0.03 % of additive and carrier oil to about 99.993-99.97 % by volume of liquid AC. Even more preferably, the ratio is about 0.009-0.02 % of additive and carrier oil to about 99.991-99.98 % by volume of liquid AC.
- odor reducing additives of the invention demonstrate the capability of the odor reducing additives of the invention to reduce odor of asphalt.
- odor reducing additives were mixed with asphalt in sealed vials.
- the headspace of the sealed vials was evaluated by gas chromatography/mass spectroscopy (GC/MS).
- GC/MS data indicated that the headspace of asphalt samples containing odor reducing additives contained reduced amounts of oil volatiles compared to the headspace of asphalt samples not containing odor reducing additives.
- Odor reducing additive X contains Thyme, Cinnamon, Pine Needle, Pine wood, Aniseed, Lemon, the reaction product of tu ⁇ entine oil and acid and subsequent fractionation, and orange oil.
- the additive is diluted with carrier oil at a volume ratio of about 3 % additive to about 97 % of carrier oil.
- Odor reducing additive Y contains (+) limonene, pine extract, pine white oil, pinus sylvestris oil, anise seed oil, clove bud oil and other miscellaneous oils.
- the additive is diluted with carrier oil at a volume ratio of about 3 % additive to about 97 % of carrier oil.
- Vial 6422-1 had an average nonualized total peak area of 14,266 +1-5% counts.
- Vial 6422-2 (containing 1 ⁇ L of X oil) had an average normalized total peak area of 14,735 +1-5% counts (FIG. 4).
- Vial 6422-3 (containing 1 ⁇ L of Y oil) produced no detectable hydrocarbon peaks (FIG. 5). Three aliquot samples of 6422-3 were run with identical results. (Minimum detection limit was approximately 500 counts). Vial 7022-1 had an average normalized total peak area of 1494 +1-5% counts.
- Vial 7022-2 (containing 1 ⁇ L of X oil) produced no detectable hydrocarbon peaks. (FIG. 7). Three aliquot samples of 7022-2 were run with identical results. (Minimum detection limit was approximately 500 counts). Vial 7022-3 (containing 1 ⁇ L of Y oil) produced no detectable hydrocarbon peaks (FIG. 8). Three aliquot samples of 7022-3 were run with identical results. (Minimum detection limit was approximately 500 counts).
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Civil Engineering (AREA)
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- Fats And Perfumes (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2004236734A AU2004236734B2 (en) | 2003-05-02 | 2004-04-30 | Additives and methods for reducing odor |
EP04751196.9A EP1620532B1 (en) | 2003-05-02 | 2004-04-30 | Additives and methods for reducing odor |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/428,233 | 2003-05-02 | ||
US10/428,233 US7037955B2 (en) | 2003-05-02 | 2003-05-02 | Additives and methods for reducing odor |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2004099352A2 true WO2004099352A2 (en) | 2004-11-18 |
WO2004099352A3 WO2004099352A3 (en) | 2006-11-09 |
Family
ID=33310356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2004/013704 WO2004099352A2 (en) | 2003-05-02 | 2004-04-30 | Additives and methods for reducing odor |
Country Status (4)
Country | Link |
---|---|
US (2) | US7037955B2 (en) |
EP (1) | EP1620532B1 (en) |
AU (1) | AU2004236734B2 (en) |
WO (1) | WO2004099352A2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007037534A1 (en) | 2007-08-09 | 2009-02-12 | Air & D - Sarl | Odor reduction process for bitumen |
WO2009083156A1 (en) * | 2007-12-21 | 2009-07-09 | Air & D - Sarl | Method for reducing malodorous substances in tank containers |
KR101481169B1 (en) | 2008-07-25 | 2015-01-12 | 현대자동차주식회사 | Deodorizing method for recycling rubber waste |
US10323199B2 (en) * | 2016-07-09 | 2019-06-18 | Ssr Pharma Private Ltd | Fuel supplement to reduce harmful emissions |
US11274208B2 (en) | 2016-10-12 | 2022-03-15 | Shell Oil Company | Reducing crumb rubber modified bitumen odors |
Families Citing this family (32)
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EP1497344B1 (en) * | 2002-04-25 | 2006-06-14 | Neville Chemical Europe B.V. | Improved modifiers for coatings, adhesives or sealants |
US6749677B2 (en) * | 2002-08-07 | 2004-06-15 | Michael Freisthler | Asphalt sealer composition |
ITMI20031390A1 (en) * | 2003-07-08 | 2005-01-09 | Turispharma S R L | EXTRACTION METHOD OF ACTIVE MOLECULAR STRUCTURES FROM NATURAL RESINS AND / OR ESSENTIAL OILS. |
US7556849B2 (en) * | 2004-03-25 | 2009-07-07 | Johns Manville | Low odor faced insulation assembly |
JP4515137B2 (en) * | 2004-04-20 | 2010-07-28 | 株式会社東海 | Liquid fuel for combustion equipment |
US6987207B1 (en) * | 2005-03-03 | 2006-01-17 | Alan Jeffrey Ronyak | Hydrocarbonaceous composition |
US20060215483A1 (en) * | 2005-03-25 | 2006-09-28 | Gary Helf | Asphalt pavement recycling method and compositions |
US7659232B1 (en) * | 2005-08-08 | 2010-02-09 | Novel Wares, Inc. | Garden tool maintenance fluid |
US20070048342A1 (en) * | 2005-08-23 | 2007-03-01 | Hauber Robert J | Anti-microbial and anti-fungal additives to provide mold and mildew resistance |
CN100366714C (en) * | 2005-11-04 | 2008-02-06 | 抚顺平天蜡制品有限公司 | Health-care candle with Chinese medicinal herb |
US20070270524A1 (en) * | 2006-05-18 | 2007-11-22 | Kerns Kelley J | Composition of matter and method of application for elimination of odors in shell sand encapsulation |
CA2655162A1 (en) * | 2006-06-12 | 2008-04-03 | Carus Corporation | Compositions for bioremediation and methods for using |
PL2190929T3 (en) * | 2007-08-23 | 2014-03-31 | Innophos Inc | Asphalt emulsion priming compositions and methods of use |
FR2929617A1 (en) * | 2008-04-04 | 2009-10-09 | Edwige Malysza | PERFUMED PATINA FOR RECOVERING SURFACES, FOR EXAMPLE WALL WALLS |
US8425678B2 (en) * | 2008-06-18 | 2013-04-23 | Owens Corning Intellectual Capital, Llc | Low odor asphalt compositions and low odor asphalt produced therefrom |
US9631093B2 (en) | 2011-12-07 | 2017-04-25 | Owens Corning Intellectual Capital, Llc | Methods for reducing odors in asphalt |
US8556536B2 (en) | 2009-01-02 | 2013-10-15 | Heatwurx, Inc. | Asphalt repair system and method |
US8562247B2 (en) | 2009-01-02 | 2013-10-22 | Heatwurx, Inc. | Asphalt repair system and method |
US8287635B2 (en) * | 2009-02-10 | 2012-10-16 | Green Product Solutions, Inc. | Asphalt mix workable at ambient temperatures with only biodegradable solvents and method of manufacturing the same |
US20100319865A1 (en) * | 2009-06-19 | 2010-12-23 | Weyerhaeuser Nr Company | Pulp for Odor Control |
US9416499B2 (en) | 2009-12-31 | 2016-08-16 | Heatwurx, Inc. | System and method for sensing and managing pothole location and pothole characteristics |
US8801325B1 (en) | 2013-02-26 | 2014-08-12 | Heatwurx, Inc. | System and method for controlling an asphalt repair apparatus |
IN2012DE00299A (en) | 2011-02-15 | 2015-04-10 | Flow Polymers Llc | |
CN103048416A (en) * | 2011-10-14 | 2013-04-17 | 西安千禾药业有限责任公司 | Detection method of Chinese medicinal composition for treating acute and chronic prostatitis |
MX2014014545A (en) * | 2012-05-30 | 2015-02-20 | Green Source Energy Llc | Composition and method for reducing hydrocarbon friction and drag in pipeline flow. |
US9976033B2 (en) | 2013-06-20 | 2018-05-22 | Greenroof Materials Llc | Voc-free asphalt-based compositions |
USD700633S1 (en) | 2013-07-26 | 2014-03-04 | Heatwurx, Inc. | Asphalt repair device |
JP6973220B2 (en) * | 2018-03-20 | 2021-11-24 | 日油株式会社 | Deodorant for asphalt |
US11987706B2 (en) | 2018-07-30 | 2024-05-21 | Dow Global Technologies Llc | Elastomer composition |
EP3911723B1 (en) * | 2019-01-17 | 2024-05-08 | The Lubrizol Corporation | Traction fluids |
CN113604058B (en) * | 2021-08-19 | 2022-05-03 | 浙江大学 | Organic volatile component capturing and converting agent and application thereof |
CN117004237A (en) * | 2023-07-11 | 2023-11-07 | 重庆市智翔铺道技术工程有限公司 | High-performance asphalt odor-removing and deodorizing additive composition, and preparation and application thereof |
Citations (1)
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WO2001036354A1 (en) | 1999-11-16 | 2001-05-25 | Alan Jeffrey Ronyak | Hydrocarbonaceous composition containing odor suppressant |
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US5271767A (en) * | 1991-10-07 | 1993-12-21 | Asphalt Control Systems Inc. | Odor-free hot-mix asphalt composition |
US20030026823A1 (en) * | 2000-06-05 | 2003-02-06 | The 54 Group, Ltd. | Environmentally safe insect repellent composition |
-
2003
- 2003-05-02 US US10/428,233 patent/US7037955B2/en not_active Expired - Lifetime
-
2004
- 2004-04-30 EP EP04751196.9A patent/EP1620532B1/en not_active Expired - Lifetime
- 2004-04-30 AU AU2004236734A patent/AU2004236734B2/en not_active Ceased
- 2004-04-30 WO PCT/US2004/013704 patent/WO2004099352A2/en active Application Filing
-
2006
- 2006-03-08 US US11/370,319 patent/US7306666B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001036354A1 (en) | 1999-11-16 | 2001-05-25 | Alan Jeffrey Ronyak | Hydrocarbonaceous composition containing odor suppressant |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007037534A1 (en) | 2007-08-09 | 2009-02-12 | Air & D - Sarl | Odor reduction process for bitumen |
WO2009083156A1 (en) * | 2007-12-21 | 2009-07-09 | Air & D - Sarl | Method for reducing malodorous substances in tank containers |
KR101481169B1 (en) | 2008-07-25 | 2015-01-12 | 현대자동차주식회사 | Deodorizing method for recycling rubber waste |
US10323199B2 (en) * | 2016-07-09 | 2019-06-18 | Ssr Pharma Private Ltd | Fuel supplement to reduce harmful emissions |
US11274208B2 (en) | 2016-10-12 | 2022-03-15 | Shell Oil Company | Reducing crumb rubber modified bitumen odors |
Also Published As
Publication number | Publication date |
---|---|
EP1620532A2 (en) | 2006-02-01 |
US7037955B2 (en) | 2006-05-02 |
AU2004236734B2 (en) | 2009-01-15 |
US7306666B2 (en) | 2007-12-11 |
EP1620532B1 (en) | 2014-02-26 |
AU2004236734A1 (en) | 2004-11-18 |
US20040220295A1 (en) | 2004-11-04 |
EP1620532A4 (en) | 2011-04-20 |
WO2004099352A3 (en) | 2006-11-09 |
US20060155003A1 (en) | 2006-07-13 |
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