EP1230331A1 - Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention - Google Patents
Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtentionInfo
- Publication number
- EP1230331A1 EP1230331A1 EP00971481A EP00971481A EP1230331A1 EP 1230331 A1 EP1230331 A1 EP 1230331A1 EP 00971481 A EP00971481 A EP 00971481A EP 00971481 A EP00971481 A EP 00971481A EP 1230331 A1 EP1230331 A1 EP 1230331A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- lamellar crystallites
- organic phase
- use according
- lamellar
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- 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
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- 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
- C10M171/06—Particles of special shape or size
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/055—Particles related characteristics
- C10N2020/06—Particles of special shape or size
-
- 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
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
Definitions
- the present invention relates to the use, as extreme pressure additives in aqueous lubricants, of lamellar crystallites. It also relates to these lamellar crystallites as well as their production.
- the present invention relates to the use in aqueous lubricants, as extreme pressure additives of lamellar crystallites, of micron size, and comprising a stack of organic phases and aqueous solutions; said crystallites being dispersed within the aqueous lubricant. It has in fact been found that these lamellar crystallites, the length of which is less than or equal to 100 ⁇ m, the width less than or equal to 30 ⁇ m and the thickness less than or equal to 200 nm, come into contact with the surface of the metal to be transformed , and that they promote lubrication, by a sliding of the lamellar crystallites relative to each other, during the transformation / deformation operation.
- the appended figure represents a photograph taken by transmission electron microscopy (Cryo-MET; full scale of the photograph: 2 ⁇ m). It represents lamellar crystallites according to the invention.
- the present invention therefore has for first object the use as an extreme pressure additive used in aqueous lubricants used for the deformation or the transformation of metals, of lamellar crystallites of length (L) between 0.1 and 100 ⁇ m, of width (I) between 0.5 and 30 ⁇ m and of thickness (e) between 5 and 200 nm, comprising a stack of organic phases (O) and aqueous solutions (A) according to the sequence O / [A / O] n, n being an integer other than 0 and such that the stack has a thickness of 5 to 200 nm, the organic phases comprising: i) at least one acid chosen from:
- a second object of the invention consists of such lamellar crystallites.
- Another object of the invention consists in obtaining the lamellar crystallites.
- the method consists in bringing into contact a solution or a dispersion comprising the acid optionally neutralized, with the metal being in an ionic and / or metallic form.
- a second variant for obtaining the lamellar crystallites according to the invention consists in preparing an aqueous mixture comprising the polymer and then in raising locally the temperature of the mixture above the cloud point temperature of said block polymer. This temperature rise more particularly takes place in the vicinity of the metal surface to be treated / deformed, in particular with the release of heat resulting from the friction or deformation of the metal.
- the lamellar crystallites will first be described.
- said lamellar crystallites have a length of between 0.1 and 100 ⁇ m.
- the length of the lamellar crystallites is between 0.5 and 20 ⁇ m.
- the lamellar crystallites also have a width varying between 0.5 and 30 ⁇ m. More particularly, the width of the lamellar crystallites is between 0.5 and 10 ⁇ m.
- the thickness of the lamellar crystallites is between 5 and 200 nm, preferably between 10 and 100 nm.
- the dimensions of the lamellar crystallites which have just been indicated correspond to average values. In other words, there is a size distribution of the lamellar crystallites, the average of which falls within the above ranges.
- the lamellar crystallites more particularly consist of a stack of organic phases (O) and aqueous solutions (A) according to the sequence 0 / [A / 0] n, n being an integer different from 0 and such that l stack has a thickness of 5 to 200 nm.
- n is a positive integer which can be at most equal to 100.
- n is an integer between 1 and 20.
- the lamellar crystallites comprise organic phases consisting of at least one acid and at least one metal in the form of a multivalent ion.
- the acid used in the composition of said organic phases is chosen from:
- said acid is optionally in a form neutralized by an organic or mineral base.
- organic phases can comprise either a single type of acid or a mixture of these two types. They may likewise comprise, in each of these types, a single acid or else a mixture of several of them.
- carboxylic acids capable of entering into the composition of the organic phases of the lamellar crystallites according to the invention are chosen from mono- or poly-carboxylic acids, saturated or not, comprising 5 to 40 carbon atoms.
- they correspond to the following formula:
- R1 - COOH formula in which R 1 represents an alkyl, alkenyl radical having one or more ethylenic unsaturations, linear or branched, having from 5 to 40 carbon atoms (the carbon atom of the carboxylic group being included), optionally substituted by one or more radicals hydroxyls and / or at least one carboxylic function.
- the acid corresponds to the above formula, in which R 1 represents an alkyl radical comprising 7 to 30 carbon atoms, optionally substituted by one or more hydroxyl radicals and / or one or more , preferably one, carboxylic functions.
- the second carboxylic function may or may not be at the end of the chain.
- the organic phase i) derives from at least one fatty acid, more particularly comprising a single carboxylic function.
- fatty acid more particularly comprising a single carboxylic function.
- saturated fatty acids mention may be made of stearic, palmitic and behenic acids.
- unsaturated fatty acids there may be mentioned unsaturated fatty acids having a single double bond such as linderic, myristoleic, palmitoleic, oleic, petroselenic, doeglic, gadoleic, erucic acids; unsaturated fatty acids having two double bonds such as linoleic acid; unsaturated fatty acids having 3 double bonds such as linolenic acid; unsaturated fatty acids having more than 4 double bonds such as isanic, stearodonic, arachidonic, chypanodonic acids; unsaturated fatty acids carrying a hydroxyl group such as ricinoleic acid and their mixtures.
- R which may or may not be identical, represent a hydrocarbon radical comprising 1 to 30 carbon atoms
- A is a linear or branched alkylene radical comprising 2 to 4 carbon atoms
- y which is an average value, is between 0 and 100
- x and x 'are equal to 1 or 2, provided that x + x' 3.
- R is an aliphatic, cycloaliphatic or aromatic hydrocarbon radical, saturated or unsaturated, containing 1 to 30 carbon atoms.
- the radicals R which are identical or different, are alkyl or alkenyl radicals carrying one or more ethylenic unsaturations, linear or branched, containing 8 to 26 carbon atoms.
- radicals R which may or may not be identical, may be aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents; these radicals comprising 6 to 30 carbon atoms.
- aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents; these radicals comprising 6 to 30 carbon atoms.
- non-phenyl, mono-, di- and tri-styrylphenyl radicals may be mentioned, among others.
- the group OA corresponds to an oxyethylenated, oxypropylenated, oxybutylenated radical, or their mixtures.
- said group corresponds to an oxyethylenated and / or oxypropylenated radical.
- the acid used in the composition of the organic phases of the lamellar crystallites is optionally in a form neutralized by a mineral or organic base.
- suitable bases capable of being used to neutralize the acid suitable are the basic compounds creating monovalent species.
- bases used are preferably water-soluble.
- hydroxides hydroxycarbonates, carbonates, bicarbonates, of alkali metals, ammonia.
- Suitable organic bases mention may be made in particular of primary, secondary or tertiary amines, comprising 1 to 40 carbon atoms, optionally substituted by one or more hydroxyl radicals, and / or one or several oxyalkylenated groups.
- Said alkylene groups are preferably oxyethylene units.
- the number of oxyalkylenated units, if they are present, is less than or equal to 100.
- Suitable amines there may be mentioned monoethanolamine, diethanolamine, ethylenediamine, aminoethylethanolamine, aminomethylpropanolamine.
- Polyoxyalkylenated fatty amines can also be used as organic base, such as those sold by Rhodia
- the lamellar crystallites further comprise at least one metal in the form of a multivalent ion. More particularly, said metal can be in the form of a divalent ion or even a trivalent ion. It is likewise not excluded to use several metals, with identical or different degrees of oxidation.
- said metal is chosen from columns IIA, VIII, IB, IIB, with the exception of cobalt and nickel. More particularly, the metals are chosen from calcium, magnesium, copper, zinc, iron, aluminum.
- the lamellar crystallites can comprise a mixture of at least two metals.
- the lamellar crystallites comprise a mixture of two metals, which preferably are zinc and copper.
- the organic phases of the lamellar crystallites comprise at least one polyoxyalkylenated block polymer having a cloud point.
- the cloud point designates the temperature of the critical point in the phase diagram of the polymer with water, corresponding to the appearance of an attraction between the micelles giving rise to the coexistence of a self-organized phase. lamellar and a solution.
- the polyoxyalkylenated block polymer used in the composition of the organic phases ii) has a cloud point of between 30 ° C and 90 ° C.
- the block polymers preferably have a molecular weight by weight of between 500 and 50,000 g / mole (measured by GPC, polyethylene glycol standard).
- the polymers suitable for the present invention comprise oxyethylenated and oxypropylenated and / or oxybutylenated units.
- block polymers have a proportion of oxyethylenated / (oxypropylenated and / or oxybutylenated) units between 1.5 and 5.
- the block polymers comprise oxyethylenated and oxypropylenated units.
- lamellar crystallites comprising organic phases of type ii
- the use of the latter takes place by locally raising the temperature of the medium in which said lamellar crystallites are dispersed, at a temperature greater than or equal to that of the cloud point of said block polymer.
- Such local elevation can advantageously take place in the vicinity of the metal surface to be treated / deformed. Indeed, during processing or deformation, heating of the metal surface generally occurs.
- the amount of lamellar crystallites dispersed in the aqueous lubricant during its use usually represents 0.1 to 5% by weight relative to the total weight of the lubricant during its use.
- the amount of lamellar crystallites is between 0.1 and 1% by weight relative to the same reference.
- the lamellar crystallites according to the invention can be used in the presence of at least one nonionic surfactant.
- nonionic surfactants that may be mentioned, among others, without however intending to be limited thereto:
- polyoxyalkylenated C8-C22 aliphatic alcohols .
- polyoxyalkylenated triglycerides .
- polyoxyalkylenated fatty acids .
- polyoxyalkylenated sorbitan esters .
- amides of C8-C20 fatty acids optionally polyoxyalkylenated.
- polyoxyalkylenated units if they are present, of these nonionic surfactants usually varies from 2 to 100. It should be noted that by polyoxyalkylenated units, the oxyethylenated, oxypropylenated, or their mixtures, are designated.
- the surfactant content usually varies between 0 and 5% relative to the total weight of lubricant during its use.
- the lamellar crystallites having organic phases of type i) can be obtained by bringing a solution or a dispersion comprising the optionally neutralized acid into contact with the metal which is in an ionic and / or metallic form .
- dispersion is meant a dispersion of vesicles, droplets or else micelles in an aqueous medium.
- a dispersion it may be advantageous to use a dispersion comprising at least one nonionic surfactant, such as in particular chosen from the list indicated above.
- the surfactant content usually varies, if it is present, between 1 and 30% by total weight of the concentrated dispersion.
- the latter can be either in its metallic form or in the form of a multivalent cation.
- Said cation can itself be in the form of a solid, a solution or a dispersion.
- the metal is used in the form of a solution, preferably aqueous
- a solution preferably aqueous
- salts of mineral acids such as halides, with chlorides for example; nitrates, as well as salts of organic acids such as formate, acetate, among others.
- the metal in the form of oxide, hydroxide, carbonate, or of the metal itself.
- the contacting is carried out in the presence of at least one compound having the effect of buffering the pH. More particularly, one or more compounds are chosen so that the pH of the medium is between 7 and 9, preferably between 8 and 8.5.
- the contact takes place with stirring.
- the metal is introduced in the chosen form, into the solution or dispersion of the acid optionally neutralized with the above-mentioned mineral or organic base.
- the operation advantageously takes place at a temperature below 100 ° C, and preferably at a temperature between 20 and 60 ° C.
- the lamellar crystallites having organic phases of type ii) can be obtained by preparing an aqueous mixture comprising the polymer and then locally raising the temperature of said mixture to a value at least greater than or equal to that of the point of cloudiness of said polymer.
- the lamellar crystallites according to the invention are therefore used, and this constitutes another object of the present invention, as an extreme pressure additive in aqueous lubricants used for the deformation or transformation of metals.
- deformation is understood to mean in particular the drawing operations, rolling. Processing operations refer more specifically to metal cutting work.
- the metals which can be the subject of such treatments are in particular, and mainly, steels, stainless steels, aluminum, copper, zinc, tin, copper-based alloys (bronze, brass), etc. .
- aqueous lubricants comprising the lamellar phases according to the invention are used in the operations of drawing of brass-plated steel wires.
- Aqueous lubricants are generally colloidal dispersions in water. It should be noted that the dispersions can be emulsions, or else dispersions of solid particles or of organized phases in an aqueous medium. Aqueous lubricants generally have a pH between 7 and 9.
- They can also include the conventional additives in this field, such as preserving agents, anti-corrosion agents, anti-foaming agents, stabilizing agents.
- the lamellar crystallites according to the invention can be indifferently introduced into a bath for treating or deforming the metal, new or used.
- the lamellar crystallites according to the invention can be introduced into the bath in the form of precursors.
- the bath in the case of lamellar crystallites consisting of organic phases i), it is possible to add to the bath, on the one hand the optionally neutralized acid solution, and on the other hand, the metal in the required form.
- the block polymer having a cloud point which will transform into lamellar crystallites as soon as the temperature locally reaches a value at least equal to that of the cloud point of said polymer.
- H3PO4 / diethanolamine sufficient quantity to have a pH between 8 and 8.5 (buffer)
- the resulting mixture is then diluted 10 times.
- Brass powder (15 g / l) is then added thereto with stirring, at 40 ° C.
- the mixture is left for 5 days with stirring at the temperature indicated above. It is found, by analysis by transmission electron microscopy, that the mixture contains lamellar crystallites.
- the figure indeed shows lamellar crystallites of section between 50 and 100 nm and of length greater than 2-3 ⁇ m (full scale of the figure: 2 ⁇ m).
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9913139 | 1999-10-21 | ||
FR9913139A FR2800091B1 (fr) | 1999-10-21 | 1999-10-21 | Utilisation de micro-lamelles en tant qu'additifs extreme-pression dans des lubrifiants aqueux, micro-lamelles et leur obtention |
PCT/FR2000/002944 WO2001029159A1 (fr) | 1999-10-21 | 2000-10-23 | Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1230331A1 true EP1230331A1 (fr) | 2002-08-14 |
EP1230331B1 EP1230331B1 (fr) | 2005-04-06 |
Family
ID=9551181
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00971481A Expired - Lifetime EP1230331B1 (fr) | 1999-10-21 | 2000-10-23 | Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention |
Country Status (14)
Country | Link |
---|---|
US (1) | US6806238B1 (fr) |
EP (1) | EP1230331B1 (fr) |
JP (2) | JP2003528940A (fr) |
KR (1) | KR100523717B1 (fr) |
CN (1) | CN100345950C (fr) |
AT (1) | ATE292668T1 (fr) |
AU (1) | AU772577B2 (fr) |
BR (1) | BR0014935B1 (fr) |
CA (1) | CA2387820C (fr) |
DE (1) | DE60019327T2 (fr) |
ES (1) | ES2235968T3 (fr) |
FR (1) | FR2800091B1 (fr) |
MX (1) | MXPA02003685A (fr) |
WO (1) | WO2001029159A1 (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2820431B1 (fr) * | 2001-02-06 | 2007-04-27 | Rhodia Chimie Sa | Procede de deformation de metaux mettant en oeuvre un lubrifiant aqueux additive permettant d'augmenter la productivite |
KR100591778B1 (ko) * | 2005-01-19 | 2006-06-26 | 몽 필 김 | 곡물 분쇄기 |
AT502630B1 (de) * | 2005-10-21 | 2008-01-15 | Miba Sinter Austria Gmbh | Bauelement, insbesondere formteil, mit einer beschichtung |
US7449432B2 (en) * | 2006-03-07 | 2008-11-11 | Ashland Licensing And Intellectual Property, Llc (Alip) | Gear oil composition containing nanomaterial |
CN106350190B (zh) * | 2016-08-19 | 2019-04-30 | 湖北省化学工业研究设计院 | 一种高强镀黄铜钢丝拉拔润滑剂及其制备方法 |
WO2022099300A1 (fr) | 2020-11-05 | 2022-05-12 | Ardagh Metal Beverage USA Inc. | Formulations pour le travail des métaux avec des formulations d'inhibiteurs de corrosion |
KR102477036B1 (ko) | 2022-05-26 | 2022-12-19 | 주식회사 에스에이치엘 | 습식윤활액 조성물 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3036118A (en) * | 1957-09-11 | 1962-05-22 | Wyandotte Chemicals Corp | Mixtures of novel conjugated polyoxyethylene-polyoxypropylene compounds |
US4452711A (en) * | 1983-01-20 | 1984-06-05 | Aluminum Company Of America | Aqueous metalworking lubricant containing polyoxypropylene-polyoxyethylene-polyoxypropylene block copolymers |
US5964692A (en) * | 1989-08-24 | 1999-10-12 | Albright & Wilson Limited | Functional fluids and liquid cleaning compositions and suspending media |
GB8926885D0 (en) * | 1989-11-28 | 1990-01-17 | Albright & Wilson | Drilling fluids |
US5807810A (en) * | 1989-08-24 | 1998-09-15 | Albright & Wilson Limited | Functional fluids and liquid cleaning compositions and suspending media |
US6166095A (en) * | 1993-12-15 | 2000-12-26 | Albright & Wilson Uk Limited | Method of preparing a drilling fluid comprising structured surfactants |
PL317709A1 (en) * | 1994-06-13 | 1997-04-28 | Du Pont | Steel corrosion inhibitors composition |
FR2758561B1 (fr) * | 1996-11-25 | 1999-04-23 | Rhodia Chimie Sa | Compositions d'orthophosphates soufres, leur procede de preparation et leur utilisation |
JPH11279581A (ja) * | 1998-03-26 | 1999-10-12 | Kyodo Yushi Co Ltd | 金属加工用水溶性油剤 |
FR2777902B1 (fr) * | 1998-04-28 | 2002-03-15 | Rhodia Chimie Sa | Utilisation dans un lubrifiant de trefilage,d'une suspension d'un sel de cobalt comme agent d'adherence,suspension et son obtention |
-
1999
- 1999-10-21 FR FR9913139A patent/FR2800091B1/fr not_active Expired - Fee Related
-
2000
- 2000-10-23 AU AU10330/01A patent/AU772577B2/en not_active Ceased
- 2000-10-23 US US10/111,002 patent/US6806238B1/en not_active Expired - Lifetime
- 2000-10-23 CN CNB008145687A patent/CN100345950C/zh not_active Expired - Lifetime
- 2000-10-23 EP EP00971481A patent/EP1230331B1/fr not_active Expired - Lifetime
- 2000-10-23 MX MXPA02003685A patent/MXPA02003685A/es active IP Right Grant
- 2000-10-23 WO PCT/FR2000/002944 patent/WO2001029159A1/fr active IP Right Grant
- 2000-10-23 AT AT00971481T patent/ATE292668T1/de not_active IP Right Cessation
- 2000-10-23 ES ES00971481T patent/ES2235968T3/es not_active Expired - Lifetime
- 2000-10-23 KR KR10-2002-7005010A patent/KR100523717B1/ko active IP Right Grant
- 2000-10-23 CA CA002387820A patent/CA2387820C/fr not_active Expired - Fee Related
- 2000-10-23 BR BRPI0014935-7A patent/BR0014935B1/pt not_active IP Right Cessation
- 2000-10-23 JP JP2001531946A patent/JP2003528940A/ja active Pending
- 2000-10-23 DE DE60019327T patent/DE60019327T2/de not_active Expired - Lifetime
-
2009
- 2009-08-07 JP JP2009184750A patent/JP2009287030A/ja active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO0129159A1 * |
Also Published As
Publication number | Publication date |
---|---|
AU1033001A (en) | 2001-04-30 |
DE60019327D1 (de) | 2005-05-12 |
ATE292668T1 (de) | 2005-04-15 |
BR0014935A (pt) | 2002-06-11 |
JP2003528940A (ja) | 2003-09-30 |
KR20020052192A (ko) | 2002-07-02 |
ES2235968T3 (es) | 2005-07-16 |
AU772577B2 (en) | 2004-04-29 |
CN1382203A (zh) | 2002-11-27 |
EP1230331B1 (fr) | 2005-04-06 |
FR2800091A1 (fr) | 2001-04-27 |
WO2001029159A1 (fr) | 2001-04-26 |
BR0014935B1 (pt) | 2011-03-22 |
KR100523717B1 (ko) | 2005-10-26 |
US6806238B1 (en) | 2004-10-19 |
JP2009287030A (ja) | 2009-12-10 |
CA2387820A1 (fr) | 2001-04-26 |
CN100345950C (zh) | 2007-10-31 |
DE60019327T2 (de) | 2006-05-04 |
FR2800091B1 (fr) | 2005-01-28 |
CA2387820C (fr) | 2007-05-01 |
MXPA02003685A (es) | 2003-10-14 |
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