EP2215200A2 - Procédé de fabrication d'une composition organique contenant un n-nonyléther - Google Patents
Procédé de fabrication d'une composition organique contenant un n-nonylétherInfo
- Publication number
- EP2215200A2 EP2215200A2 EP08852039A EP08852039A EP2215200A2 EP 2215200 A2 EP2215200 A2 EP 2215200A2 EP 08852039 A EP08852039 A EP 08852039A EP 08852039 A EP08852039 A EP 08852039A EP 2215200 A2 EP2215200 A2 EP 2215200A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- nonyl
- ether
- component
- nonyl ether
- 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.)
- Withdrawn
Links
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Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/03—Specific additives for general use in well-drilling compositions
- C09K8/035—Organic additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/36—Water-in-oil emulsions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/52—Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
Definitions
- the present invention relates to a process for producing an organic composition which comprises a functional component selected from the group consisting of a thermoplastic polymer, an enzyme, a binder, a paraffin, an oil, a colorant and a hair or skin care substance, and an n Nonyl ether, a process for producing a shaped article, a method for producing a packaged product, the use of at least one n-nonyl ether, the use of a shaped article, a method for cleaning the surfaces of boreholes, drilling equipment or cuttings, method for producing a Borehole and method for producing an oil or a gas.
- a functional component selected from the group consisting of a thermoplastic polymer, an enzyme, a binder, a paraffin, an oil, a colorant and a hair or skin care substance, and an n Nonyl ether
- pure alcohol and its derivatives such as, for example, ethers or esters
- Pure Cs alcohol and its derivatives are characterized by deep solidification points, but have low boiling points and are therefore very volatile.
- the branched i-nonanols are substance mixtures and are produced petrochemically. The branching of the alcohols leads to a poorer biodegradability.
- a disadvantage in connection with the use of i-nonanols is still the too high melting point or too low boiling range of the derivatives such as esters, ethoxylates, sulfates, even if alcohol mixtures are used. Due to the non-ideal viscosity behavior, especially at lower temperatures, this product group is therefore limited.
- the present invention was based on the object at least partially overcome the disadvantages resulting from the prior art.
- organic compositions comprising ethers of medium chain linear fatty alcohols can be provided as an additive, these organic compositions being comparable to those known from the prior art, organic compositions have less volatile components and have a satisfactory viscosity behavior even at low temperatures.
- the present invention the object of the invention to provide a method by means of which organic compositions containing ethers of linear fatty alcohols short to medium chain length can be provided as an additive, with as many components of these organic compositions on renewable resources or starting materials, which renewable raw materials can be obtained.
- organic compositions obtainable by this process in comparison to those known from the prior art, organic compositions have improved performance properties.
- the present invention was the object of specifying a compound Phyg, which can be used in particular as an additive in drilling fluids or cleaning agents for drilling equipment.
- the present invention relates to a process for producing an organic composition which comprises a functional component selected from the group consisting of a thermoplastic polymer, an enzyme, a binder, a paraffin, an oil, a colorant and a hair or skin care substance , containing as process steps:
- an n-nonyl ether as an additive which is obtainable by reacting an n-nonyl alcohol component with a further component which is capable of reacting with the n-nonyl alcohol component to form an n-nonyl ether,
- the functional component of a thermoplastic composition is the thermoplastic polymer, the functional component of an adhesive of the binder, the functional component of a lubricant formulation the oil, the functional component of a detergent the enzyme, the functional component of a defoamer the paraffin, the functional component of a paint or a colorant the colorant and the functional component of a cosmetic preparation Hair or skin care substance.
- an "organic composition” is preferably understood as meaning a composition which consists of more than 50% by weight, based on the total weight of the organic composition, of organic components, wherein as an organic component it is preferable to use a carbon-containing compound Exception of CO 2 , CO, carbides, CSO and pure carbon compounds such as graphite, carbon black or diamond .
- the organic component is a hydrocarbon compound having oxygen, nitrogen, phosphorus, sulfur or at least two of these atoms as heteroatoms can.
- an n-nonyl ether is initially provided as an additive which is obtainable by reacting an n-nonyl alcohol component with a further component which is in contact with the n-nonyl ether.
- Nonyl alcohol component is able to react to form an n-nonyl ether.
- n-nonyl ether preferably comprises the following process steps:
- ia2 providing a further component capable of reacting with the n-nonyl alcohol component to form an n-nonyl ether
- an n-nonyl alcohol component is initially provided.
- the n-nonyl alcohol component to at least 80 wt .-%, more preferably at least 90 wt .-% and most preferably at least 99 wt. %, in each case based on the provided n-nonyl alcohol component, is obtained from pelargonic acid.
- the catalytic hydrogenation of esters of pelargonic acid for example the catalytic hydrogenation of the methyl, ethyl, propyl or butyl ester of pelargonic acid.
- the pelargonic acid itself can be obtained for example by ozonolysis of oleic acid and subsequent, oxidative work-up of the oleic ozone or by ozonolysis of
- the preparation of oleic acid can again be effected from tallow or tall oils, as described, for example, in US 6,498,261
- the pelargonic acid can also be obtained by ozonolysis of oleic acid or erucic acid by isomerization of petrochemical raw materials, and the petrochemical production of pelargonic acid is also conceivable, as described, for example, by Harold A., Witteoff, Bryan G., Reuben, Jeffrey S. Plotkin in, J 7 UtS and OiIs ", Industrial Organic Chemicals ( Second Edition) (2004), John Wiley & Sons, Inc., pp. 411-434, or the preparation of pelargonic acid from oleic acid according to the method described in GB-A-813842.
- the n-nonyl alcohol component used for the preparation of the n-nonyl ether contains, in addition to the n-nonyl alcohol, further alcohols, for example Cs and / or Cio alcohols, but in this case it is particularly preferred that the n-nonyl alcohol component is less than 10% by weight, more preferably less than 7.5% by weight, and most preferably less than 5% by weight, based in each case on the n-nonyl alcohol component , Cs and Cio alcohols.
- the proportion of n-nonyl alcohol in the n-nonyl alcohol component is in the case of use a mixture of n-nonyl alcohol and at least one further alcohol, preferably at least 90% by weight, more preferably at least 92.5% by weight and most preferably at least 95% by weight, based in each case on the total weight of the n-nonyl alcohol Component.
- n-nonyl alcohol component is in particular that n-Nonylalkohol- component which is obtained by catalytic hydrogenation of the products marketed under the brand name EMERY ® 1202 EMERY ® 1203 and Emery ® 1210 pelargonic acid, wherein EMERY ® 1202 less than 1 Wt .-% of C ⁇ monocarboxylic acids, about 1 wt .-% of C 7 - monocarboxylic acids, about 4 wt .-% of Cs monocarboxylic acids, about 93 wt .-% of pelargonic acid and about 2 wt.
- EMERY ® 1202 less than 1 Wt .-% of C ⁇ monocarboxylic acids, about 1 wt .-% of C 7 - monocarboxylic acids, about 4 wt .-% of Cs monocarboxylic acids, about 93 wt .-% of pelargonic acid and about 2 wt.
- EMERY ® weight 1203 about 0.1 wt .-% of C ⁇ -Cs-monocarboxylic acids, to about 99 wt .-% of pelargonic acid and about 0.9.
- step ia2) of the process for providing an n-nonyl ether at least one further component which is reacted with the n-nonyl alcohol
- Component with the formation of an n-nonyl ether is provided, whereby this further component is preferably an alcoholic compound. hol, an epoxide, a haloalkane or a mixture of at least two of them.
- this alcohol is selected from the group consisting of cis to C 3 o-alkanols, particularly preferably ci to C 2 o-alkanols and most preferably Ci- to C.
- Ci- to C3o-diols such as methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, octanol and nonanol
- Ci- to C3o-diols more preferably from Ci- to C 2O -DiO len and most preferably ci- to Cio-diols such as glycol and propanediol
- Ci- to C3o-triols more preferably from Ci- to C 2O -TnO len and most preferably Ci- to Cio-triols, such as glycerol, polyalcohols or polyether alcohols, such as Diethylene glycol, dipropylene glycol, triethylene glycol, triethylene glycol, tetraethylene glycol, tetrapropylene glycol, polyethylene glycols having a molecular weight of more than 100 g / mol, polypropylene glycol
- epoxides of C 2 to C 2 O hydrocarbons and more preferably C 2 to C 14 hydrocarbons are preferably used, with ethylene oxide, propylene oxide and glycidol particularly preferred epoxides and ethylene oxide and propylene oxide am most preferred epoxides.
- Other suitable components are epoxystearic acid and diepoxylinoleic acid or derivatives thereof.
- halogen alkane in particular chlorine alkanes, such as 1-chloro-butane, 2-chloro-butane, 1-chloro-pentane, 2-chloro-pentane or 3-chloro-pentane into consideration.
- the n-nonyl alcohol component is reacted with the at least one component to form an n-nonyl ether.
- the condensation of the alcohols under dehydration is preferably carried out continuously, in particular in a fixed bed reactor which is charged with suitable catalysts is, such as with alumina moldings, in particular with ⁇ -alumina, preferably in the form of pellets, tablets, extrudates, spheres or granules, or with zeolite-based catalyst systems.
- suitable catalysts such as with alumina moldings, in particular with ⁇ -alumina, preferably in the form of pellets, tablets, extrudates, spheres or granules, or with zeolite-based catalyst systems.
- the condensation is preferably carried out at temperatures of from 200 ° C. to 260 ° C., more preferably from 220 ° C. to 260 ° C. and at a pressure of from 10 mbar to 60 bar.
- the condensation takes place in the gas and / or liquid phase.
- the optimum temperatures depend on the educt (s) used, the progress of the reaction, the type of catalyst and the catalyst concentration. They can easily be determined by experiment for each individual case. Higher temperatures increase the reaction rates and promote side reactions, such as dehydration from alcohols or formation of colored by-products.
- a suitable process for preparing an ether using haloalkanesulfonic acids as catalysts is described, for example, in DE-A-195 11 668.
- the crude product obtained in this way usually consists of a mixture of starting material, olefins and dialkyl ethers, which can be separated, for example, by distillation, wherein the unreacted alcohol is preferably recycled back into the process.
- dialkyl ethers by condensation of diols is described, for example, in DE-A-10 2004 056 786 or in WO-A-97/035823, the disclosure of which with respect to the preparation of dialkyl ethers from alcohols is hereby introduced as a reference and a part of Disclosure of the present invention forms.
- n-nonyl ether is prepared as a further component by substitution reaction between the alcohols in the n-nonyl alcohol component and an epoxide, for example ethylene oxide or propylene oxide
- the reaction is preferably carried out in the presence of suitable catalysts, such as zeolites or hydrophobicized hydrotalcites
- suitable catalysts such as zeolites or hydrophobicized hydrotalcites
- the reaction of ethylene oxide and propylene oxide with, for example, alcohols to give polyethoxylated or multiply propoxylated ethers is described, for example, in DE-A-40 10 606, the disclosure of which relates to the preparation of dialkyl ethers from alcohols and ethylene oxide or propylene oxide herewith as a reference and forms part of the disclosure of the present invention.
- the n-nonyl ether provided in process step i) is a polyether alcohol having 2 to 30 ether repeat units, more preferably having 4 to 20 repeat units, wherein these ether-repeating units are preferably a - [0-CH 2 -CH 2 ] unit, a - [0-CH 2 -CH 2 -CH 2 ] unit or a mixture of these units.
- Such polyether alcohols can be obtained by reacting the n-nonyl alcohol component in a condensation reaction with a polyethylene glycol of corresponding chain length or by reacting the n-nonyl alcohol component in a substitution reaction with ethylene oxide, propylene oxide or a mixture of ethylene oxide and propylene oxide is implemented in such relative amounts that 2 to 30 ether repeat units, particularly preferably 4 to 20 ether repeating units are bound to the n-nonyl alcohol component.
- n-nonyl ether but in particular that described above, be supported on n-nonyl ether.
- Nonyl alcohol based polyether alcohol as a modified n-nonyl ether in
- the process for providing an n-nonyl ether comprises the further process step of
- the acid component for the esterification it is possible to use all organic and inorganic acids known to the person skilled in the art, which are capable of reacting with OH functional organic compounds. Particularly preferred according to the invention is the use of mono-, di- or polycarboxylic acids.
- Suitable monocarboxylic acids in this context are, for example, acetic acid, butyric acid, acrylic acid, methacrylic acid, oleic acid, oxalic acid, stearic acid, succinic acid, citric acid, fumaric acid, maleic acid, benzoic acid or citric acid, while as dicarboxylic acids, for example, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid , Pimelic, suberic, azelaic, sebacic, tartaric, malic, ⁇ -ketoglutaric, oxaloacetic, orthophthalic, isophthalic or terephthalic acid.
- dicarboxylic acids for example, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid , Pimelic, suberic, azelaic, sebacic, tartaric, malic, ⁇ -ketoglutaric, o
- a suitable tricarboxylic acid is, for example, trimellitic acid.
- inorganic acids such as, for example, sulfuric acid, phosphoric acid or boric acid, so that the corresponding sulphates, phosphates or borates are obtained.
- Sulfonic acids such as, for example, benzenesulfonic acid, n-nonylsulfonic acid, dodecylbenzenesulfonic acid, dodecylbenzenesulfonate, dodecylbenzenesulfonic acid, ammonium dodecylbenzenesulfonate, benzenesulfonic acid or dodecylbenzenesulfonic acid, can also be used as the acid. Also conceivable is the use of a mixture of at least two of the abovementioned acid components, in particular the use of a mixture of an organic and of an inorganic acid.
- the acid component is reacted with the n-nonyl ether in such a proportion that the molar ratio of carboxylic acid groups: hydroxyl groups in a range of 1: 1.0 to 1: 5.0, more preferably in a range of 1: 1.2 to 1: 2, and most preferably in a range of 1: 1, 7 to 1: 1.9.
- the esterification is preferably carried out in the presence of an esterification catalyst.
- esterification catalysts acids such as sulfuric acid or p-toluenesulfonic acid, or metals and their compounds can be used. Suitable examples are tin, titanium, zirconium, which are used as finely divided metals or expediently in the form of their salts, oxides or soluble organic compounds.
- the metal catalysts are achieved in contrast to proton acids high-temperature catalysts that did their full activi- usually only at temperatures above 180 0C. However, they are preferred according to the invention, because they provide less by-products, such as Olef ⁇ ne compared to the proton catalysis.
- esterification catalysts are one or more divalent tin compounds or tin compounds or elemental tin, which can react with the starting materials to divalent tin compounds.
- catalyst tin tin (II) chloride, tin (II) sulfate, tin (II) alcoholates or tin (II) salts of organic acids, in particular of mono- and dicarboxylic acids.
- Particularly preferred tin catalysts are tin (II) oxalate and tin (II) benzoate.
- the esterification reaction can be carried out by methods known to the person skilled in the art.
- the esterification reaction it is preferable to conduct the esterification reaction at a temperature in a range of 50 to 300 ° C., more preferably in a range of 100 to 250 ° C., and most preferably in a range of 150 to 200 ° C.
- the optimum temperatures depend on the alcohol (s) used, the progress of the reaction, the type of catalyst and the catalyst concentration and can easily be determined by experiment for each individual case.
- a functional component is provided.
- the functional component is a thermoplastic polymer and the organic composition is therefore a thermoplastic, organic composition.
- thermoplastic polymer refers to plastics that can be easily (thermo-plastic) deformed in a certain temperature range.This process is reversible and can be as often as desired by cooling and reheating to the molten state be repeated, as long as the thermal decomposition of the material does not start due to overheating.
- thermoplastic polymers which can be used as the functional component according to the first variant of the inventive method, are generally polycondensates or chain polymers or a mixture of these two, in particular thermoplastic polyurethanes, thermoplastic polyesters, thermoplastic polyamides, thermoplastic polyolefins, thermoplastic polyvinyl esters, thermoplastic polyethers , thermoplastic polystyrenes, thermoplastic polyimides, thermoplastic sulfur polymers, thermoplastic polyacetals, thermoplastic fluoroplastics, thermoplastic styrene-olefin copolymers, thermoplastic
- thermoplastic ethylene-vinyl acetate copolymers Polyacrylates, thermoplastic ethylene-vinyl acetate copolymers or mixtures of two or more of the above-mentioned thermoplastic polymers in question.
- thermoplastic polymer to more than 90 wt .-%, more preferably more than 95 wt .-%, more preferably at least 99 wt .-% and most preferably to 100 wt. -%, based in each case on the total weight of the thermoplastic polymer, based on thermoplastic polyesters.
- polyester includes, in particular, polymers produced by a polycondensation reaction between a polycarboxylic acid and a polyol (so-called “LA / BB polyester”) or by polycondensation reaction of a hydroxycarboxylic acid or by ring-opening polymerization of a cyclic ester (
- polycarbonates which are obtainable by reaction of phosgene with diols may be excluded from the term "polyester” used according to the invention.
- thermoplastic polyesters and copolyesters can be used.
- polyesters include in Substantially linear polyesters which have been prepared via a condensation reaction of at least one polycarboxylic acid, preferably a dicarboxylic acid (diacid) or an ester-forming derivative thereof and at least one polyol, preferably a dihydric alcohol (diol).
- the preferred dibasic acid and preferably divalent diol may both be either aliphatic or aromatic, but aromatic and partially aromatic polyesters are particularly preferred as thermoplastic molding materials in view of their high softening points and hydrolytic stability.
- aromatic polyesters essentially all ester linkages to the aromatic ones are
- Attached rings They can be semi-crystalline and even exhibit liquid crystalline behavior or be amorphous.
- Partially aromatic polyesters which have been obtained from at least one aromatic dicarboxylic acid or an ester-forming derivative thereof and at least one aliphatic diol are thermoplastic compounds which are particularly preferred according to the invention
- polyester examples include terephthalic acid, 1,4-naphthalenedicarboxylic acid, or 4,4'-
- Suitable aliphatic diols include alkylene diols, especially those containing 2 to 6 C atoms, preferably 2 to 4 C atoms, in which case in particular ethylene glycol, propylene diols and butylene diols may be mentioned.
- ethylene glycol, 1,3-propylene diol or 1,4-butylene diol are used as the polyol or diol component for the production of the thermoplastic polyester contained in the composition according to the invention as component a).
- particularly preferred thermoplastic polyesters which are characterized by
- Polyalkylene terephthalate PET
- polypropylene terephthalate PPT
- polybutylene terephthalate PBT
- polyalkylene naphthalates for example, polyethylene naphthalate (PEN) or polybutylene naphthalate (PBN)
- polylactic acid PPA
- polyalkylene dibenzoate te, for example Polyethylenbibenzoat and mixtures of at least two of these thermoplastic polyesters.
- These partially aromatic polyesters described above may optionally contain a small amount of units selected from others
- Dicarboxylic acids for example, isophthalic acid, or other diols, such as cyclohexanedimethanol, are derived, which generally reduces the melting point of the polyester.
- a special group of partially aromatic polyesters are so-called segmented or block copolyesters, which additionally contain the aforementioned polyester segments (also called “hard segments"), so-called “soft segments”.
- These soft segments are made of a flexible polymer; that is, a substantially amorphous polymer having a low glass transition temperature (T g ) and low rigidity, with reactive end groups, preferably two hydroxyl groups.
- T g glass transition temperature
- Soft segments below 0 ° C., more preferably below -20 ° C., and most preferably below -40 ° C.
- Suitable examples of "soft segments” are aliphatic polyethers, aliphatic Polyester or aliphatic polycarbonates.
- the molecular weight of the soft segments may vary within wide limits, but is preferably between 400 and 6,000 g / mol.
- linear polyesters which via a polycondensation reaction of at least one polycarboxylic acid or a
- thermoplastic polyesters which are obtainable by polycondensation of short-chain hydroxycarboxylic acids or by ring-opening reaction of cyclic esters.
- suitable short-chain hydroxycarboxylic acid which can be used for the preparation of thermoplastic polymers include in particular L-lactic acid, D-lactic acid, DL-lactic acid, glycolic acid, 3-hydroxybutyric acid, 4-hydroxybutyric acid, 4-hydroxyvaleric acid, 5-
- Suitable cyclic esters include glycolide (a dimer of glycolic acid) and ⁇ -caprolactone (a cyclic ester of 6-hydroxycaproic acid).
- thermoplastic polyesters The preparation of the thermoplastic polyesters described above is also described, inter alia, in the "Cyclopedia of Polymer Science and Engineering", Volume 12, pages 1-75 and pages 217-256, John Wiley & Sons (1988) and also in “Ullmann's Encyclopedia of Industrial Chemistry, Vol. A21, pages 227 to 251, VCH Publishers Inc. (1992).
- Thermoplastic polymers preferred according to the invention are polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and polylactic acid (PLA).
- PET polyethylene terephthalate
- PBT polybutylene terephthalate
- PLA polylactic acid
- this thermoplastic polymer as the functional component in an amount of at least 60 wt .-%, preferably of at least
- n-nonyl ether as an additive, in particular as a mold release agent, as an antifogging agent, as a plasticizer, as Antistatikmit- or as a lubricant, preferably in an amount in the range of 0.001 to 40% by weight, more preferably in an amount in the range of 0.01 to 25% by weight, and most preferably in an amount in the range of 0.1 to 10 wt .-%, each based on the total weight of the thermoplastic composition is used.
- the n-nonyl ether is a polyalkylene glycol ether of the n-nonanol, more preferably a polyethylene glycol ether or polypropylene glycol ether of the n-nonanol and most preferably a poly ethylene glycol ether of n-nonanol is, wherein the polyalkylene glycol, which was used for the preparation of the polyalkylene glycol, preferably has a molecular weight of more than 100 g / mol.
- additives which can be provided according to this first variant of the inventive method in process step ic), in particular Schalgzähmaschinebuchsmodifikatoren, filler materials, reinforcing agents, flame retardant compounds, heat and UV stabilizers, antioxidants, other processing aids, nucleating agents, dyes and anti-drip agents in question.
- suitable Schalgzähmaschinebuchsmodifikatoren filler materials, reinforcing agents, flame retardant compounds, heat and UV stabilizers, antioxidants, other processing aids, nucleating agents, dyes and anti-drip agents in question.
- Impact modifiers, filler materials, reinforcing agents and flame retardant compounds can be found inter alia US 2005/0234171 Al. These other additives are preferably used in an amount in a range of 0.001 to 20 wt .-%, particularly preferably in an amount in a range of 0.01 to
- thermoplastic composition 10 wt .-% and most preferably in an amount in a range of 0.1 to 5 wt .-%, each based on the total weight of the thermoplastic composition used.
- the mixing of the n-nonyl ether, the functional component (thermoplastic polymer) and optionally the additive, which takes place in the case of the first variant of the process according to the invention in process step ii), can be carried out using known techniques.
- the blending may be a dry blending operation where the various components are below the melt processing temperature of the thermoplastic polymer, or a melt mixing process in which the components, optionally premixed and mixed at the melt processing temperatures of the thermoplastic polymer.
- the melt mixing method is the preferred melt edge method according to the present invention, which is obtained by, for example, continuous melt kneading using a single-screw kneader, a twin-screw kneading machine of the same directional rotation type, gear different directional rotation type, non-serration equal direction Rotation type, non-serration different direction rotation type, or others
- Types or by batch melt kneading using a Walzenknetmaschine, a Banbury-Rnetmaschine or the like can be realized. Also conceivable is a combination of a dry mixing process and a melt mixing process.
- the order and the manner of addition of the individual components ia), ib) and optionally ic) in the mixing device is basically not critical.
- initially the thermoplastic polymer and optionally the additives can be initially charged in the mixing device and only then the n-nonyl ether can be added.
- the mixing takes place according to at least one of the following measures: Ml) at the glass transition temperature of the thermoplastic polymer or at a temperature above the glass transition temperature of the thermoplastic polymer; M2) wherein the n-nonyl ether is more liquid than the thermoplastic polymer; or M3) wherein at least a portion of the n-nonyl ether is added to the precursor of the thermoplastic polymer.
- the mixing of the components provided in process steps ia), ib) and optionally ic) in process step ii) of the process according to the invention is carried out by a melt mixing process.
- the mixing in process step ii) takes place at the glass transition temperature of the thermoplastic polymer or at a temperature above the glass transition temperature of the thermoplastic polymer.
- the mixing at a temperature in a range of 5 degrees below the glass transition temperature (T g ) to 200 0 C above the glass transition temperature of the thermoplastic polymer used, more preferably at a temperature in a Be - ranging from 1 degree below the glass transition temperature (T g) to 180 0 C above the glass transition temperature of the thermoplastic polymer, and most preferably (T g) at a temperature in a range from 1 degree above the glass transition temperature to 150 0 C above the glass transition temperature of the thermoplastic polymer used, but the upper limit of the temperature range is essentially limited by the decomposition temperature of the thermoplastic polymer used. Furthermore, it corresponds to embodiments of the invention, when the mixing takes place at temperatures in a range of 10 to 180 0 C and preferably 50 to 150 0 C above the glass transition temperature of the thermoplastic polymer used.
- the n-nonyl ether is more liquid than the thermoplastic polymer
- the n-nonyl ether is used at a temperature at which it is liquid and the thermoplastic polymer is not yet liquid.
- the temperature of the thermoplastic polymer is below the glass transition temperature of this polymer.
- the melting temperature of the n-nonyl ether and the glass transition temperature of the thermoplastic polymer at least 5 ° C, preferably at least
- thermoplastic polymer 10 0 C and more preferably at least 30 0 C distinguish. Furthermore, it is in this embodiment and also generally preferred to use the thermoplastic polymer as granules. In general, all granule forms known to those skilled in the art with spherical or cylindrical spatial form are also contemplated herein.
- the granule size determined by sieve analysis is in a range of 0.01 to 5 cm and preferably in a range of 0.1 to 4 cm for at least 70% by weight of the granule particles.
- the surfaces of the granule particles can be at least partially coated with the n-nonyl ether, so that at least partially coated thermoplastic polymer granules is obtained. This allows the most homogeneous possible distribution of the n-nonyl ether according to the invention in the thermoplastic composition, especially if this is formulated as a formulation for the subsequent extrusion.
- n-nonyl ethers in liquid and also in solid form are suitable.
- a precursor of the thermoplastic polymer basically all precursors known to those skilled in the art are considered prior to obtaining the thermoplastic polymer. These include in particular precursors which have a lower molecular weight than the final thermoplastic polymer. In this case, it is preferred that the molecular weight of the precursor be at least 1.1, preferably at least 1.5, and more preferably at least 2, of that of the finished thermoplastic polymer.
- thermoplastic polymer which preferably consist of 2 to 100 monomers
- a prepolymer which is polymerized, usually by heat treatment, to form the finished thermoplastic polymer is based
- the functional component is an enzyme and the organic composition is a detergent.
- Suitable enzymes are in particular amylases, proteases, lipases, cellulases, peroxidases or mixtures of at least two of these enzymes.
- Amylases are added to remove starch and glycogen. Suitable for use according to the invention are alpha, beta and gamma amylases, as well as
- Glucoamylases and maltogenic amylases are commercially available for example under the names Duramyl ®, Termamyl ®, Fungamyl ® and BAN ® (Novo Nordisk), and Maxamyl ®, Purafect ® OxAm the o-.
- the amylases can come from any source, such as bacteria, fungi, animal pancreatic glands
- amylase enzymes can be used in the compositions according to the invention in an amount of from 0.0001% by weight to 5% by weight, more preferably from 0.0001% by weight to 1% by weight and most preferably from 0.0005 to 0.5 wt .-%, each based on the total weight of the organic composition, are present.
- proteases for cleaving proteins and peptide residues can also be added to the organic compositions according to the invention in accordance with the second variant of the method according to the invention.
- Proteases are particularly suitable for the hydrolytic cleavage and removal of protein residues, in particular dried-on protein residues.
- Proteases which are suitable according to the invention are proteinases (endopeptidases) and peptidases (exopeptidases).
- Useful proteases may be of plant, animal, bacterial and / or fungal origin. Suitable proteases are in particular serine, cysteine, aspartate and metal proteases. Also genetically modified proteases are, if appropriate even preferred, usable in the inventive compositions.
- proteases are commercially available under the names Alcala- se ®, BLAP ®, Durazym ®, Esperase ®, Everlase® ®, Maxapem ®, Maxatase ®, options timase Purafect ® OxP or Savinase ®.
- proteases are used in an amount of from 0.00001 to 1.5% by weight and more preferably from 0.0001 to 0.75% by weight, based in each case on the total weight of the organic composition.
- lipases can be used as a functional component according to the second variant of the method according to the invention. They serve to remove firmly adhering greasy soil. Lipases are thus a biosynthetic
- Suitable lipases can be obtained from plants (for example, Rhizinus species), microorganisms and animal sources, such as pancreatic lipases. Commercially available lipases are, for example, Lipolase ®, Lipomax® ®, ® and Lipozym Lumafast® ®.
- the above-mentioned enzymes may optionally be combined with any other enzymes to improve the purification performance of the
- Detergent used to further improve organic composition is Detergent used to further improve organic composition.
- Further enzymes which are suitable according to the invention are cellulases, hemicellulases, peroxidases, reductases, oxidases, ligninases, cutinases, pectinases, xylanases, phenoloxidases, lipoxygenases, tannases, pentosanases, sen, malanases. Glucanases, arabinosidases and any mixtures of these enzymes.
- the n-nonyl ether is preferably added to the detergent in the function of a surfactant, in which case it is preferred for the n-nonyl ether to be present in an amount of 0.001 to 40% by weight, more preferably of 0.01 to 30 wt .-%, more preferably from 0.1 to 20 wt .-% and most preferably from 1 to 10 wt .-%, each based on the total weight of the organic composition is used.
- additives which can be provided in process step ic) according to this second variant of the process according to the invention, there are in particular further surfactants, builders, solvents, hydrophobic components, phase separation auxiliaries, thickeners, polymers, soil release, different from the n-nonyl ether Active ingredients, solubilizers, hydrotropes, such as, for example, sodium cumene sulphonate, octylsulfate, butylglucoside, butylglycol, emulsifiers, such as gallus soap, gloss-drying additives, cleaning intensifiers, antimicrobial agents or antidotes, antistatics, preservatives, such as glutaraldehyde,
- Bleaching systems perfumes, fragrances, dyes, opacifiers or skin protection agents, wherein the amount of such additives is usually not more than 12 wt .-%, based on the total weight of the organic composition.
- the functional component is a binder and the organic composition is an adhesive.
- the chemical composition of the binder contained in the adhesive depends on how it is set by the adhesive.
- it can be a physically setting adhesive, for example a hotmelt adhesive comprising, for example, ethylene-vinyl acetate copolymers, polyamides or polyesters as binders, a solvent-containing wet adhesive comprising, for example, polymeric vinyl compounds, polymethyl methacrylate or natural and synthetic rubber as a binder a contact adhesive, including, for example
- Polychloroprene or butadiene-acrylonitrile rubber as a binder a dispersion adhesive containing, for example, polyvinyl acetate, vinyl acetate copolymers, polyacrylates, polyvinylidene chloride, styrene-butadiene copolymers, polyurethanes, polychloroprene or rubber latexes as binder, a water-based adhesive containing, for example, glutinic glues , such as skin glue or fish glue, glues based on natural vegetable products, such as starch glue, methyl cellulose or casein glue, or PVAL adhesives as a binder, a pressure-sensitive adhesive, including for example polyacrylates, polyvinyl ethers or natural rubber as a binder, or a Plastiso 1, including, for example, PVC and plasticizers as binders, act.
- a dispersion adhesive containing, for example, polyvinyl acetate, vinyl acetate copolymers, poly
- Adhesive for example a cyanoacrylate-based adhesive, including, for example, cyanoacrylic acid ester as a binder, a methylacrylate methacrylate-based adhesive, including, for example, methacrylic acid methyl ester as a binder, an anaerobic curing adhesive comprising, for example, diacrylic esters of diols as curing agents, a radiation-curable adhesive comprising, for example, epoxy acrylates or polyester acrylates as binders, a phenol-formaldehyde resin-based adhesive containing, for example, phenols and Formaldehyde as a binder, a silicone-based adhesive, including, for example, polyorganosiloxanes as a binder, a polyimide-based adhesive, including, for example, aromatic tetracarboxylic anhydrides and aromatic diamines as binders, an epoxy resin adhesive comprising, for example, oligomeric diepoxides and polyamines or polyamido
- the concentration of binder in the adhesive is dependent on the type of adhesive used, but is usually in a range of 10 to 100 wt .-%, more preferably from 20 to 90 wt .-% and more preferably from 30 to 80 wt. -%, in each case based on the total weight of the adhesive.
- the n-nonyl ether is preferably added to the adhesive in the function of a solvent, a condenser or else in the function of a surfactant, in which case it is preferred for the n-nonyl ether to be present in one
- Amount of 0.001 to 40 wt .-%, particularly preferably from 0.1 to 30% by weight, more preferably from 1 to 20 wt .-% and most preferably from 3 to 10 wt .-%, each based on the total weight of the organic composition is used.
- the concentration of the n-nonyl ether may optionally also be above the above-mentioned concentration ranges.
- the additives which can be provided according to this third variant of the process according to the invention in method step ic) depend on the nature of the particular adhesive.
- the amount of such additives depends on the nature of the particular adhesive and is usually not more than 50 wt .-%, based on the total weight of the organic composition.
- the functional component is a paraffin, in particular a paraffin wax, and the organic composition is a defoamer.
- the paraffin provided as a functional component in the fourth variant of the process according to the invention in process step ib) generally represents a complex substance mixture without a sharp melting point.
- its melting range is usually determined by differential thermal analysis (DTA) as described in "The Analyst” (1962), 420, and / or its solidification point. This is the temperature at which the wax passes from the liquid to the solid state by slow cooling.
- DTA differential thermal analysis
- Paraffins with less than 17 carbon atoms are not useful according to the invention, their proportion in the paraffin wax mixture should therefore be as low as possible and is preferably below the limit which can be measured with conventional analytical methods, for example gas chromatography.
- waxes are used, which solidify in the range of 20 0 C to 70 0 C.
- paraffin wax mixtures may contain different proportions of liquid paraffin.
- the liquid fraction is as high as possible at 40 0 C without amount at this temperature already 100%.
- Particularly preferred paraffin wax mixtures have at 40 ° C. a liquid fraction of at least 50% by weight, in particular of
- paraffin waxes contain less than 1 wt .-%, in particular less than 0.5 wt .-% at 110 0 C and atmospheric pressure vaporizable fractions. According to the invention Paraffin waxes can be obtained for example under the trade names Luna Flex ® from fillers and Deawax ® DEA Mineralöl AG.
- the amount of paraffin in the defoaming organic composition is preferably in a range of 50 to 99% by weight, more preferably 60 to 95% by weight, and most preferably 70 to 95% by weight, respectively based on the total weight of the organic composition. If, however, carrier materials are added to the defoamer, the proportion of Parafin also be well below the above concentration ranges.
- the n-nonyl ether is preferably added to the defoamer in the function of a solvent or else in the function of a surfactant, in which case it is preferred for the n-nonyl ether to be present in an amount of 0.001 to 20% by weight %, more preferably from 0.1 to 10% by weight, even more preferably from 1 to 8% by weight and most preferably from 2 to 7% by weight, based in each case on the total weight of the organic composition, is used.
- the additives which can be provided in process step ic) according to this fourth variant of the process according to the invention may be, for example, silicone oils and their mixtures with hydrophobicized silica, or further defoaming compounds such as, for example, bisamides.
- the defoamer may also contain carrier materials which preferably have a granular structure and consist of water-soluble or water-dispersible, surfactant-free compounds, in particular of inorganic and / or organic salts which are suitable for use in detergents and cleaners.
- water-soluble, inorganic support materials are in particular alkali metal carbonate, alkali metal borate, alkali aluminosilicate and / or alkali metal sulfate, while as organic carrier materials, for example acetates, tartrates, succinates, citrates, carboxymethylsuccinates and the alkali metal salts of aminopolycarboxylic acids, such as EDTA, hydroxyalkanephosphonates and Aminoalkanpolyphosphonate in question, such as l-hydroxyethane-l, l-diphosphonate, Ethylendiaminotetramethy- lenphosphonat and Diethylentriaminpentamethylenphosphonat can be used.
- organic carrier materials for example acetates, tartrates, succinates, citrates, carboxymethylsuccinates and the alkali metal salts of aminopolycarboxylic acids, such as EDTA, hydroxyalkanephosphonates and Amin
- film-forming polymers such as Polyethylene glycols, polyethylene glycols, polyvinylpyrrolidones, polyacrylates and cellulose derivatives as support materials are conceivable, for example.
- the amount of such additives is usually not more than 25% by weight, based on the total weight of the organic composition.
- carrier materials can also be used in a significantly higher concentration.
- defoamer which can be prepared according to the fourth variant of the method according to the invention mentioned in WO-A-1997/034983 defoamers are mentioned, in particular, the disclosure of this document with respect to the method for producing a defoamer from the in the Process steps Ia, Ib and Ic) provided in the sense of process step ii) is hereby incorporated by reference and forms part of the disclosure of the present invention.
- the functional component is an oil, preferably a hydrocarbon having 20 to 35 carbon atoms (lubricating oil), and the organic composition is a lubricant formulation.
- the oil contained in the lubricant formulation may be a raffinate obtained by separating hydrocarbons naturally present in petroleum with 20 to 35 carbon atoms, a hydrocracking oil (HC synthesis oil) obtained by cracking petroleum constituents greater than 35% Carbon atoms, or by synthetic hydrocarbons obtained by cracking petroleum constituents of less than 12 carbon atoms into gases such as, in particular, ethene or butene and the subsequent synthesis of hydrocarbons having 20 to 35 carbon atoms can be obtained from these gases.
- HC synthesis oil hydrocracking oil
- bio-oils obtained from renewable raw materials may also be present in the lubricant formulation, in particular
- Bio oils from the HETG, HEPG, HEPR or HEES group can be used.
- the HETG group includes triglycerides, such as rapeseed oil, while the HEPG group comprises polyglycols.
- the HEES group includes synthetic esters, in particular TMP esters (trimethylpropane esters, also called esters of oleic acid or trioleate).
- the HEPR group includes liquids consisting mainly of polyalphaolefins (PAO) and related hydrocarbons.
- the amount of oil in the lubricant formulation is preferably in the range of 50 to 99% by weight, more preferably in the range of 60 to 95% by weight, and most preferably in the range of 70 to 90% by weight. %, in each case based on the total weight of the organic composition.
- the lubricant formulation may also have large amounts of water, in which case the oil content in the lubricant formulation may well be well below the above-mentioned concentration ranges.
- the n-nonyl ether is added preferably in the function of a solvent or in the function of a surfactant of the lubricant formulation, in which case it is preferred that the n-nonyl ether in an amount of 0.001 to 40 wt %, more preferably from 0.1 to 30% by weight, even more preferably from 1 to 20% by weight and most preferably from 2 to 10 wt .-%, each based on the total weight of the organic composition is used.
- the additives which can be provided in process step ic) according to this fifth variant of the process according to the invention can be, in particular, surface-active, oil-improving or oil-protecting additives.
- Surface-active additives include detergents, dispersants, high-pressure or wear protection, corrosion and rust protection, and friction-modifying additives.
- the oil-improving additives change the properties of the oil in terms of viscosity, pour point and elastomers, for example of seals.
- the oil-protective additives prevent the oil from aging, deactivate metal particles and prevent the oil from foaming. Even finely ground solids, such as Teflon (PTFE), ceramic oxides or Mo lybdändisulf ⁇ d- compounds can be added as an additive.
- the lubricant composition may also contain water in amounts of up to 95% by weight, more preferably in amounts of up to 90% by weight, in which case the lubricant composition preferably in the form of an emulsion.
- the functional component is a colorant and the organic composition is a lacquer or a color.
- a "color” is understood to mean a non-shiny, open-pored coating with a high proportion of dye and pigment, but only a low binder content, while a “coat” means a composition for coating surfaces of wood, metal , Plastic or mineral material understood which has a higher binder content compared to a paint.
- the colorant may be an inorganic or an organic colorant, which colorants may be water-soluble or water-insoluble.
- inorganic or organic, preferably powdered pigments are suitable. Pigments differ from dyes in that they are insoluble in their application media. Suitable inorganic pigments and their preparation methods may be G. Buxbaum; Industrial Inorganic Pigments ", 1st edition,
- colorants may be present in the paint or in the paint in amounts ranging from 0.001 to 40% by weight, more preferably in amounts in one
- the n-nonyl ether is added preferably in the function of a solvent or in the function of a surfactant to the paint or the color, in which case it is preferred that the n-nonyl ether in an amount of 0.001 to 40% by weight, more preferably from 0.1 to 30% by weight, even more preferably from 1 to 20% by weight and most preferably from 2 to 10% by weight, based in each case on the total weight of organic composition is used.
- the additives which can be provided in process step ic) according to this sixth variant of the process according to the invention may in particular be binders, such as vegetable oils, coniferous gum rosin, casein from milk, alkyd resin, polyurethane resin or epoxy resin, solvents, such as water , Ethanol, citrus peel oil, white spirit, water or glycol ethers, thixotropic agents, antioxidants, viscosity regulators, skin and foam inhibitors, leveling agents, UV absorbers, extenders, preservatives or binders.
- the amount of additives to be used can vary widely. This applies in particular to the binders and solvents, depending on whether it is a paint or a paint. 7.
- the functional component is a hair or skin care substance and the organic composition is a cosmetic preparation.
- hair and / or skin care substances are in particular 18-.beta.-glycyrrhetinic acid from liquorice root extract (Gylcyrrhiza glabra), preferably in a purity of> 99% pure substance in the extract, aescin in horse chestnut (Aesculus hippocastanum), allantoin, aloe vera ( containing mainly sugars, anthraquinones and minerals such as zinc), amino acids such as alanine, arginine, serine, lysine, ammonium glycyrrhizate from licorice root extract, preferably in a purity of almost 100% pure substance in the extract, apigenin from chamomile extract (Matri) caria recutita), Arnica, in particular Arnica montana or Arnica chamissonis, Asiaticoside and Madecassoside in Centella asiatica extract, Avenonaanthramide from oat extract (Avena sativa), Avocadol
- John's wort St. John's wort extract (Hypericum perforatum), jojoba oil, lecithin, corn oil (Zea mays), evening primrose oil, niacinamide, oenotheine B in the extract of fireweed (Epilobium angustifolium), oleuropein in olive extract (Olea europea), phytocresin (sodium Beta-sitosterol sulphate), plankton extract (tetraselmis suecica, spirulina and others), polyphenols, catechins from the extract of
- Grape seeds (Vitis vinifera), polyphenols, catechins from green tea (Camellia sinensis), marigold extract (Calendula off ⁇ cinalis), rosemary acid in melissa extract (Melissa off ⁇ cinalis), sandorn oil, oat glucans (Avena sativa), stearylglycyrrhetinic acid (stearyl ester the 18-beta-beta glycyrrhetinic acid), sterols, sitosterol in stinging nettle extract (Urtica dioca),
- Sweet almond oil (Prunus dulcis), vitamin C and its esters, vitamin E and its esters, wheat germ oil zinc gluconate / magnesium aspartate / copper gluconate, zinc sulfate or zinc oxide and proteins or protein derivatives such as protein hydrolysates (for example collagen, keratin, silk protein). or wheat protein hydrolysates).
- protein hydrolysates for example collagen, keratin, silk protein. or wheat protein hydrolysates.
- These hair and / or skin care substances may be present in the cosmetic preparations in amounts ranging from 0.001 to 40% by weight, more preferably in amounts ranging from 0.01 to 30% by weight, more preferably in amounts in a range of 0.01 to 30 wt .-%, and most preferably in amounts ranging from 0.1 to 10 wt .-%, each based on the total weight of the organic composition, be included.
- Nonyl ether preferably added in the function of a solvent or in the function of a surfactant of the cosmetic preparation, in which case it is preferred that the n-nonyl ether in an amount of 0.001 to 40 wt .-%, particularly preferably of 0.1 to 30 wt%, more preferably from 1 to 20 wt%, and most preferably from 2 to 10 wt .-%, each based on the total weight of the organic composition is used.
- Suitable additives which can be provided according to this seventh variant of the process according to the invention in method step ic) are, for example, Schrader, K., "Grundlagen und Vietnamese", 2nd edition, 1989, pages 728-737, Domsch, A ., "The Cosmetic Preparations", Verlag für chemische Industrie (H. Ziolkowsky, Ed.), 4th Edition, Volume 2 pages 212-230, 1992 or Johnson, DH, "Flair and Hair Care", New York, 1997, pages 65 to 104.
- the additives can be used in the customary amounts known to the person skilled in the art, in particular in amounts of from 0.1 to 10.0% by weight, based on the total weight of the organic composition.
- a contribution to the solution of the abovementioned objects is also provided by a method for producing a shaped body, comprising the method steps:
- thermoplastic composition obtainable by the above-described process according to the first variant
- thermoplastic composition to the glass transition temperature of the thermoplastic polymer or to a temperature above the glass transition temperature of the thermoplastic polymer;
- thermoplastic composition according to the invention is first of all prepared provided, wherein this provision is preferably carried out by a method according to the first variant of the inventive method.
- the thermoplastic composition is heated to the glass transition temperature of the thermoplastic polymer or at a temperature above the glass transition temperature of the thermoplastic polymer.
- the heating of the thermoplastic composition to a temperature in a range of 5 degrees below the glass transition temperature (T g ) to 100 0 C above the glass transition temperature of the thermoplastic polymer used, more preferably to a temperature in a range of 1 degree below the glass transition temperature (T g ) to 50 0 C above the glass transition temperature of the thermoplastic polymer used, and most preferably to a temperature in the range of 1 degree above the glass transition temperature (T g ) to 20 0 C is above the glass transition temperature of the thermoplastic polymer used, but here too the upper limit of the temperature range is essentially limited by the decomposition temperature of the thermoplastic polymer used.
- the method steps I) and II) can be carried out simultaneously or in succession.
- a simultaneous implementation of method steps I) and II) is useful, for example, if the thermoplastic composition is produced by means of a melt-blending method.
- a successive implementation of method steps I) and II) is useful, for example, if the thermoplastic composition is produced by a dry mixing process or if the thermoplastic composition is indeed produced by a melt blending method, but not immediately after the production of a molded article. rather, it is first subjected to cooling in accordance with method step v).
- a shaped body is produced from the heated, thermoplastic composition produced in process step II).
- injection molding, extrusion molding, compression molding, layer molding, lamination molding, cavity molding, vacuum molding and transfer molding are considered as a method of producing a molded article, with injection molding being particularly preferred.
- the mass cross-section is the cross-section of a region of the shaped body that consists of the thermoplastic molding composition of the invention.
- the mass cross-section represents the thickness of a wall of these containers or containers.
- the mass cross-section represents the thickness of these threads or strands.
- the mass cross section represents the strength of these flat structures.
- all methods known and suitable to the person skilled in the art come into consideration for reducing the mass fraction. This includes, for example, stretching in one or two directions, pulling in one or two directions, spinning or blowing, each preferably at elevated temperatures at which the thermoplastic composition of the invention is so soft or even liquid that stretching, pulling, spinning or Blisters can be done.
- stretching or drawing takes place when a fiber is to be obtained from the shaped body obtained in step III).
- drawing or stretching can take place in one or more dimensions.
- the web running from an extruder can be drawn onto a roll at a speed which is higher than that from the extruder in comparison with the exit speed.
- a container or container it is primarily the blowing in step IV) that is used, apart from stretching, pulling and spinning.
- the mass cross-section reduction takes place by applying a gas pressure.
- the gas pressure is generally chosen so that the usually heated to at least glass transition temperature thermoplastic composition of the molded article obtained in step III) can be stretched.
- the elongation is limited by the use of a mold having the final shape of the molded article.
- liquid containers such as freezers, trays and packaging for foods such as fruits, vegetables or meat and pharmaceuticals as tablets, capsules, suppositories or powders and containers for liquids produced.
- These liquid containers can be used in addition to liquids of the cosmetic or pharmaceutical industry in the food industry, preferably in the beverage industry as reusable containers such as PET or PLA bottles.
- two or more of the method steps I) to IV) to be supplemented by further method steps and / or to run at least overlapping in time. This applies in particular to process steps III) and IV).
- the material provided in process step a) is preferably a pharmaceutical, a personal care product, an agricultural auxiliary, an adhesive, a building material, a dye or a foodstuff.
- the at least partially surrounding the good can be done for example by the method described in DE-A-103 56 769.
- a contribution to the solution of the abovementioned objects is also provided by a method for coating substances which can be consumed by living beings, including as method steps:
- Nonyl alcohol component is able to react to form an n-nonyl ether
- n-nonyl ether at least partially surrounding the organism-consumable substance with the n-nonyl ether.
- the provision of the n-nonyl ether is preferably carried out according to process step ia) of the process described above for the preparation of an organic composition.
- the at least partial surrounding of the substance which can be consumed by living beings with the n-nonyl ether can take place, for example, in such a way that the consumable substance and the n-nonyl ether are mixed together in suitable mixing devices, in particular the Patterson-Kelley mixer, DRAIS turbulence mixer, Lödigemischer, Ruberg mixers, screw mixers, plate mixers and fluidized bed mixers as well as continuous vertical mixers in which the polymer structure is mixed by means of rotating knives in rapid frequency (Schugi mixer), as mixing devices into consideration.
- suitable mixing devices in particular the Patterson-Kelley mixer, DRAIS turbulence mixer, Lödigemischer, Ruberg mixers, screw mixers, plate mixers and fluidized bed mixers as well as continuous vertical mixers in which the polymer structure is mixed by means of rotating knives in rapid frequency (Schugi mixer), as mixing devices into consideration.
- the at least partially surrounding the edible by living things substance with the n-nonyl ether can also be done by, for example, presented by living beings in a fluidized bed mixer and submitted the n-nonyl ether in liquid form on by Living beings consumable substance is sprayed on.
- n-nonyl ether which can be obtained by reacting an n-nonyl alcohol component with a further component which reacts with the n-nonyl alcohol component to form an n-nonyl ether also contributes to the solution of the abovementioned objects to react as an additive in a composition
- a composition comprising as a functional component ⁇ ) a thermoplastic polymer, wherein the composition is a thermoplastic composition; ⁇ ) an enzyme, the composition being a detergent; ⁇ ) a binder of an adhesive, the composition being an adhesive; ⁇ ) a paraffin, the composition being a defoamer; ⁇ ) an oil, the composition being a lubricant formulation; ⁇ ) a colorant, the composition being a lacquer or a color; or ⁇ ) a hair or skin care substance, the composition being a cosmetic preparation,
- n-nonyl ether is preferably obtained by the process described above for preparing an n-nonyl ether, comprising the process steps ial), ia2), ia3) and optionally ia4).
- n-nonyl ether described at the outset, which is obtainable by reacting an n-nonyl alcohol component with a further component which reacts with the n-nonyl alcohol component to form an n-nonyl ether, also contributes to the solution of the abovementioned objects react as an additive in compositions used in drilling wells.
- n-nonyl ether described above is used as an additive in drilling fluids or cleaning agents for drilling equipment.
- the invention therefore also relates to a method for cleaning the surfaces of boreholes, in particular the walls of boreholes, conveyor or casing pipes or walls of the casing, and for cleaning boreholes. directions or cuttings, wherein the surfaces are first brought into contact with a cleaning agent containing the above-described n-nonyl ether and optionally rinsed the surfaces then with water.
- the cleaning agent is used in the form of an aqueous solution, an aqueous dispersion or an oil-in-water emulsion, including
- (cc2) 0 to 50 wt .-%, particularly preferably 0.5 to 35 wt .-%, further preferably 1.0 to 15 wt .-% and most preferably 1.2 to 10 wt .-% further, from n-nonyl ether various additives, as well
- (cc3) from 1 to 99.9% by weight, particularly preferably from 30 to 99% by weight, more preferably from 70 to 98% by weight and most preferably from 80 to 97.6% by weight of water,
- the amount of component ( ⁇ l) in the aqueous composition can vary and is adapted to the nature and extent of the contamination.
- additives other than n-nonyl ether ( ⁇ 2) there are used, in particular, infestants, fluid-loss additives, viscosity-regulating additives, wetting agents. tel or salts.
- infestants such as dirt, dirt, dust, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, smoke, and water, and water.
- organic polymer compounds of natural and / or synthetic origin may prove advantageous.
- Starch or chemically modified starches, cellulose derivatives such as carboxymethylcellulose, guar gum, synthangum or purely synthetic water-soluble and / or water-dispersible polymer compounds, in particular of the type of high molecular weight polyacrylamide compounds with or without anionic or cationic modification, may be mentioned here in particular.
- drilling equipment such as the derrick, the drill string, in particular the drill pipe and the drill bit, cleaning equipment, plant for solids disposal, in particular shakers or centrifuges, pumps, motors or gearboxes, or the drilling platform or parts thereof.
- the cleaning agent containing the n-nonyl ether is sprayed or applied to the surfaces of the objects or the objects to be cleaned are immersed in the aqueous compositions.
- the contaminants dissolve away from the surfaces.
- the surfaces are brought into contact with water so that the agents are removed together with the impurities, for example by the surface is sprayed with a jet of water.
- the cleaning agent containing the n-nonyl ether can be used for cleaning cuttings, the so-called cuttings, which accumulate during drilling and must be deposited in offshore boreholes on the bottom of the lake in the vicinity of the drilling platform
- the cuttings are cleaned beforehand and freed from the residues of the drilling fluid can be used for all cleaning operations known to those skilled in the art, which occur in the field of soil drilling, both in off-shore drilling and drilling on land. This includes in particular the removal of paraffin deposits from borehole walls.
- wellbores are cleaned by pumping a cleaning fluid under pressure through the wellbore and removing the debris from the walls of the wellbore by the cleaning agent. Subsequently, the impurities are transported with the liquid from the borehole.
- this includes the method steps
- the cleaning agent containing the n-nonyl ether is passed through the intermediate space between the outside of the casing and the walls of the borehole, preferably circulated in this intermediate space.
- This circulation may be effected, for example, by the detergent pumping down through the casing, preferably down the drill pipe, at the bottom of the casing, preferably on the drill bit or bit, and then through the space between the outside of the casing and the casing Walls of the borehole rises again. Is the cleaning agent continuously through the Pipe down pumped, can be cleaned in this way both the walls of the wellbore and the outside of the casing.
- the latter includes the step of drilling a borehole into the earth by means of a drill head driven by a drill string, wherein the cleaning agent containing the n-nonyl ether is at least partially guided through the boring head, preferably at least is partially circulated therethrough, this passage or circulation being at least partially during the presence of the drill bit in the wellbore.
- drilling equipment whose surface can be cleaned with the cleaning agent
- drilling equipment such as the derrick
- the drill string in particular the drill string and the drill bit
- cleaning equipment plant for solid disposal, in particular shakers or centrifuges, pumps, motors or gearbox, or but the drilling platform or parts thereof.
- the cleaning agent containing the n-nonyl ether is passed through the intermediate space between the outside of the casing and the walls of the borehole, preferably through this intermediate space.
- sealing liquid which is introduced in step (ß5) in the space between the outside of the conveying tube and the inside of the casing
- all known to the expert for this purpose materials can be used.
- those sealing liquids are mentioned, which are described in US 7,219,735.
- a further contribution to the solution of the abovementioned objects is also provided by a process for producing an oil or a gas which, in addition to the abovementioned process steps ( ⁇ 1) to ( ⁇ 3) and optionally ( ⁇ 4) and ( ⁇ 5), also the process steps
- the invention also relates to a method for the production of boreholes in which a drilling fluid is pumped through a borehole, wherein the drilling fluid used is a composition comprising the n-nonyl ether described in the introduction.
- this composition is a water-in-oil emulsion.
- composition is particularly preferred that the composition
- the organic oil phase I wholly or partially selected from the group of a) paraffins having 5 to 22 carbon atoms and / or b) paraffins with 5 to 22 C atoms and / or c) internal Olef ⁇ ne having 12 to 30 C atoms in the molecule and / or d) carboxylic acid esters of the general formula R-COO-R, in the R for a linear or branched, saturated or unsaturated Alkyl radical having 15 to 25 carbon atoms and R 'is a saturated, linear or branched alkyl radical having 3 to 22 carbon atoms, and / or e) mineral oils, and / or f) linear alpha-olefins (LAOs) with 12 to 30 C atoms, and / or g) carbonates.
- R-COO-R carboxylic acid esters of the general formula R-COO-R, in the R for a linear or branched, saturated or unsaturated Alkyl radical having 15 to 25 carbon
- this water-in-oil emulsion has a density of the liquid component in a range of 1.2 to 3.0 g / cm 3, and more preferably in a range of 1.5 to 3.0 g / cm 3 .
- the oil phase of the inventive systems contains the components a) to e) alone or the components a), b), d) or e) together in admixture with esters c) and optionally in admixture with other suitable oil phases. There are also any mixtures of the oil phases a) to e) with each other possible.
- linear or branched paraffins having 5 to 22 carbon atoms are used according to the invention.
- Paraffins - more correctly referred to as alkanes - are known to be saturated hydrocarbons which, for the linear or branched representatives of the general empirical formula C n H 2n + ! consequences.
- the cyclic alkanes follow the general empirical formula C n H 2n .
- Particularly preferred are the linear and branched paraffins, whereas cyclic paraffins are less preferred.
- branched paraffins are particularly preferred which are liquid at room temperature, ie those having 5 to 16 carbon atoms per molecule.
- paraffins with 17 to 22 carbon atoms, the use of a waxy consistency ways. But it is preferred to use mixtures of various fine paraffin, and it is particularly preferred that these mixtures are still liquid at 21 0 C. Such mixtures can be formed, for example, from paraffins having 10 to 21 carbon atoms. Paraffins are particularly preferred oil phases - alone or as a mixture component with further oil phases - in drilling fluids - preferably those of the invert type, in which the crosslinked glycerol or oligoglycerol esters according to the invention are used as thickeners.
- IO internal olefins
- IOs are likewise compounds known per se, which can be prepared by all methods known to the person skilled in the art.
- EP 0 787 706 A1 describes a process for the synthesis of IOs by isomerization of alpha-olefins to sulfonic or per-sulfonic acids. It is characteristic that the thus obtained IO are linear and contain at least one olefinic double bond, which is not in the alpha position of the alkyl chain located.
- such IO or 10 mixtures are used which contain IO having 12 to 30 C atoms in the molecule, preferably having 14 to 24 C atoms and in particular having up to 20 C atoms in the molecule.
- esters of the general formula R-COO-R ' in which R is a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 carbon atoms, and R' is a saturated, linear or branched alkyl radical having 6 to 22 C atoms Atoms means part of the oil phases according to the invention.
- esters are known chemical compounds. Their principal use in drilling fluids is z.
- B. Subject of EP 0374 672 Al or EP 0374 671 Al. Particularly preferred is the use of such esters whose radical R is a saturated or unsaturated alkyl radical having 15 to 25 and R 'is a saturated alkyl radical having 3 to 10 carbon atoms.
- the saturated compounds are particularly preferred.
- Mineral oils are a collective term for the liquid distillation products obtained from mineral raw materials (petroleum, lignite and coal, wood or peat), which consist essentially of mixtures of saturated hydrocarbons.
- the mineral oils contain only small amounts of aromatic hydrocarbons, preferably less than 3 wt .-%. Preference is given at 21 0 C liquid mineral oils based on petroleum.
- the mineral oils WEI sen preferably have boiling points from 180 to 300 0 C.
- LAOs Linear alpha-olefins
- alpha-C-atom monovalent unsaturated hydrocarbons that can be derived from natural products, but are also obtained synthetically on a large scale
- Natural-based LAOs are made by dehydrating natural-based fatty alcohols
- the synthetic LAOs - produced by oligomerization of ethylene - often contain straight-chain carbon numbers in the chain, but today there are also known processes for the preparation of odd-numbered alpha-olefins Because of their volatility, they generally have at least 10, preferably at least 12 to 14 C atoms in the molecule
- the upper limit of the LAO which is free-flowing at room temperature lies in the range from C 8 to C 20.
- carbonates are understood as meaning carbonic acid esters of fatty alcohols having 8 to 22 C atoms, preferably the diesters of carbonic acid.
- Such compounds and their use as oil phase for Bohr Hughesstoff are described in DE 40 18 228 Al.
- esters of Ci_ 5 monocarboxylic acids and 1- and / or polyfunctional alcohols where residues of 1-valent alcohols at least 6, preferably at least 8 C atoms and the polyhydric alcohols preferably 2 to 6 carbon atoms in the molecule have,
- the oil phase I) of the composition used as a drilling fluid in the form of a water-in-oil emulsion preferably have pour points below 0 0 C, preferably below -5 0 C (measured according to DIN ISO 3016: 1982-10) on.
- the Brookfield viscosity of the oil phase is at 0 0 C at most 50 mPas.
- the compositions used as drilling fluids, when formed as oil-based drilling mud of the W / O type have a plastic viscosity (PV) in the range of 10 to 70 mPas and a yield point YP of 5 to 60 lb / 100 ft 2 , each determined at 50 0 C, on.
- PV plastic viscosity
- the kinematic viscosity of the oil phase measured according to Ubbelohde at 20 0 C should preferably be at most 12 mm 2 / sec.
- the aqueous phase of the compositions according to the invention has preferably has a pH in the range from 7.5 to 12, preferably from 7.5 to 11 and in particular from 8 to 10.
- the composition used as the drilling fluid preferably comprises aqueous salt solutions, preferably saturated salt solutions, it being possible to use as salts all alkali metal or alkaline earth halides known to the person skilled in the art.
- suitable salts are, in particular, KCl, NaCl, LiCl, KBr, NaBr, LiBr, CaCl 2 , and MgCl 2 , among which CaCl 2 , NaCl and KCl or mixtures of these salts are particularly preferred.
- additives which may be present in the composition used as drilling mud according to component IV) are, in particular, additives selected from the group consisting of surfactants as admixing component for the crosslinked glycerol or oligoglycerol ester, weighting agents, fluid loss additives, pH modifiers, other viscosity modifying additives, wetting agents, salts, biocides, agents for inhibiting unwanted water exchange between drilled formations - e.g. B water swellable clays and / or salt layers - and the z.
- surfactants as admixing component for the crosslinked glycerol or oligoglycerol ester
- weighting agents fluid loss additives
- pH modifiers pH modifiers
- other viscosity modifying additives wetting agents
- salts e.g. B water swellable clays and / or salt layers - and the z.
- the additives may be water-soluble, oil-soluble and / or water or oil-dispersible.
- surfactants anionic, nonionic zwitterionic or cationic surfactants can be used. However, preferred are the nonionic and anionic surfactants.
- anionic surfactants are soaps, alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ethersulfates, glycerol ether sulfates, fatty acid ether sulfates, mixed hydroxy ether sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono- and dialkyl sulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts.
- nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol glycol polyethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty alcohol polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yloligoglycosides or glucuronic acid derivatives, fatty acid N-glycerides. alkyl glucamides, polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
- nonionic surfactants contain polyglycol ether chains, these may have a conventional, but preferably a narrow homolog distribution.
- the surfactants are an optional ingredient in the additives. They are preferably used in amounts of 0.01 to 2 wt .-%, in particular from 0.1 to 1.5 wt .-% and preferably from 0.2 to 0.5 wt .-%, in each case based on the total Water-in-oil emulsion, used.
- Suitable emulsifiers are preferably nonionic emulsifiers, which in particular are assigned to one of the following classes of substances: (oligo) alkoxylates, in particular lower alkoxylates, where corresponding ethoxylates and / or propoxylates are of particular importance - containing lipophilic radicals and for alkoxylation capable of basic molecules of natural and / or synthetic origin.
- Alkoxylates of the type indicated are known as such - ie with terminal free hydroxyl group on the alkoxy latrest - non-ionic emulsifiers, but the corresponding compounds may also be end-capped, for example by esterification and / or etherification.
- nonionic emulsifiers for the purposes of the invention are partial esters and / or partial ethers of polyfunctional new alcohols having in particular 2 to 6 C atoms and 2 to 6 OH groups and / or their oligomers with acids and / or alcohols containing lipophilic radicals .
- compounds of this type which additionally contain (oligo) -alkoxy radicals and in particular corresponding oligo-ethoxy radicals in their molecular structure.
- the polyfunctional alcohols having 2 to 6 OH groups in the base molecule or the oligomers derived therefrom may in particular be diols and / or triols or their oligomerization products, whereby the glycol and the glycerol or their oligomers may be of particular importance.
- the range of partial ethers of polyfunctional alcohols also includes known nonionic emulsifiers of the type of ethylene oxide / propylene oxide / butylene oxide block polymers.
- Another example of corresponding emulsifier components are alkyl (poly) glycosides of long-chain alcohols and also the already mentioned fatty alcohols of natural and / or synthetic origin or alkylolamides, amine oxides and lecithins.
- alkyl (poly) glycoside compounds APG compounds
- APG compounds alkyl glycoside compounds
- partial esters and / or partial ethers of polyhydric alcohols are in particular the corresponding partial esters with fatty acids, for example of the type of glycerol mono- and / or diesters, glycol monoesters, corresponding partial esters of oligomerized polyhydric alcohols, sorbitan partial esters and the like, and corresponding compounds with ether groups.
- organic polymer compounds of natural and / or synthetic origin may be of considerable importance in this context.
- starch or chemically modified starches cellulose derivatives such as carboxymethylcellulose, guar gum, synthangum or purely synthetic water-soluble and / or water-dispersible polymer compounds, in particular of the type of high molecular weight polyacrylamide compounds with or without anionic or cationic modification.
- Thinner for viscosity regulation The so-called diluents can be of organic or inorganic nature, examples of organic thinners are tannins and / or quebracho extract. Further examples of these are lignite and lignite derivatives, in particular lignosulfonates.
- EP 0 382 701 A1 As a preferred means against liquid loss (/ 7wz ⁇ i / oss additive) is in particular organophilic lignite, while preferred pH Modif ⁇ zierer example of EP 0 382 701 Al can be removed.
- the invention described in EP 0 382 701 A1 is based on the recognition that additives should be used in ester-based drilling fluids of the water-in-oil type which ensure that the rheological properties of the drilling fluid do not change even then, when increasing amounts of free carboxylic acids are released by partial ester hydrolysis. If possible, these free carboxylic acids should be converted into compounds which have stabilizing and emulsifying properties.
- EP 0 382 701 A1 proposes to prepare alkaline amines having a high oleophilicity and the lowest possible water solubility. which can form salts with the free acids.
- Typical examples of such amine compounds are primary, secondary and / or tertiary amines, which are predominantly water-insoluble and which moreover can be at least partially alkoxylated and / or substituted by hydroxyl groups.
- Further examples include aminoamides and / or heterocycles containing nitrogen as the ring atom.
- Suitable examples are basic amines which have at least one long-chain hydrocarbon radical having 8 to 36 carbon atoms, preferably having 10 to 24 carbon atoms, these hydrocarbon radicals may also be mono- or polyunsaturated.
- component IV) is preferably a weighting agent, such as BaSO 4 , in which case, in the case of a low added composition, component IV) is preferably used in an amount of up to 20% by weight.
- component IV) is preferably used in an amount of 20 to 50 wt .-%, while in heavily weighted compositions 50 to 70 wt .-% of component IV) can be used.
- the composition if it is present as a water-in-oil emulsion, is a nanoemulsion or a microemulsion which preferably contains water droplets or drops of an aqueous phase having a droplet size of less than 1000 .mu.m, preferably a droplet size in a range of 5 nm to 1000 microns, more preferably having a droplet size in a range of 10 nm to 850 microns, even more preferably with a drop size in a range of 20 nm to 700 ⁇ m, more preferably including a drop size in a range of 50 nm to 500 ⁇ m.
- microemulsion and "silicone emulsion” characterize emulsions which contain drops in the micrometer or nanometer range, wherein there may be some separation of these two ranges and thus also of these two terms.
- microemulsions are preferably understood to mean those emulsions which form spontaneously with a combination of the emulsion components, whereas the formation of nanoemulsions usually involves the supply of energy, for example in the form of homogenization. especially in the form of high-pressure homogenization.
- this is an aqueous solution or an oil-in-water emulsion.
- composition I 0 to 48 wt .-%, particularly preferably 0.1 to 20 wt .-% and most preferably 1 to 10 wt .-%, each based on the total weight of the composition, a water-immiscible organic oil phase , II) from 29.9 to 99.9% by weight, more preferably from 60 to 99% by weight and most preferably from 70 to 95% by weight, based in each case on the total weight of the composition, of water or aqueous phase,
- organic oil phase the aqueous phase and other additives
- those organic oil phases, aqueous phases and other additives which have already been mentioned above in connection with the water-in-oil emulsion are preferred.
- an oil-in-water emulsion as a drilling mud composition it can be prepared by any method known to those skilled in the art for making such an oil in water emulsion.
- this comprises the method steps:
- composition according to the invention in particular the composition according to the invention in the form of a water-in-oil emulsion, an aqueous solution or an oil-in-water emulsion;
- the introduction preferably the circulation preferably takes place at least partially during the drilling in method step ( ⁇ 2).
- the erfmdungshiele composition thus acts as a drilling fluid when drilling holes in the ground, preferably when drilling crude oil or natural gas.
- composition used as a drilling fluid in particular the composition used as a drilling fluid in the form of a Water-in-oil emulsion, an aqueous solution or an oil-in-water emulsion;
- a contribution to achieving the abovementioned objects is also made by a cleaning agent and a drilling fluid, preferably a drilling fluid in the form of the above-described water-in-oil emulsion or the oil-in-water emulsion described above.
- Pelargonklaremethylester was obtained, were mixed with 5 g of a 30 wt .-% solution of potassium hydroxide in methanol and heated to 100 0 C in an autoclave. At this temperature, the traces of methanol present were removed by evacuation five times and venting with nitrogen. After increasing the Reaction temperature to 150 0 C, a total of 264 g of ethylene oxide were added in portions, so that the pressure in the reactor 5x10 5 Pa not exceeded. After completion of the reaction was cooled to about 90 0 C and evacuated for the separation of remaining traces of ethylene oxide for about 15 minutes. It was a light yellow
- PET SP04 polyethylene terephthalate
- the mixing wall temperature was 40 0 C.
- 0.3 wt .-% of di-n-nonyl ether prepared in Example 1 was added as a mold release agent.
- the material was granulated on a granulator (ZSK 26Mcc) with a screw conveyor.
- thermoplastic composition For the production of moldings from the thermoplastic composition, a fully hydraulic injection molding machine with a hydraulic clamping unit type Battenfeld HM800 / 210 was used. The maximum closing force is 800 kN, the screw diameter is 25 mm. As a test tool, a tool with a tapered, rectangular core was used. To determine the demolding force, a load cell with a maximum measuring range of 2 kN was attached to the ejector rod. The pre-drying of the molding compound was carried out at about 225 ° C for about 4 hours. A significantly improved demolding with respect to a mold release agent-free molding composition was observed with the thermoplastic composition according to the invention. EXAMPLE 4: Preparation of a detergent
- a polyol mixture for a standard polyurethane hot melt adhesive QR 6202, Henkel
- a hot melt adhesive was prepared.
- 5% by weight of the nonyl diethylene glycol ether prepared in Example 2 was added.
- Example 1 2 wt .-% bisamide, 3 wt .-% sodium carbonate, 58.7 wt .-% sodium sulfate, 21.4 wt .-% sodium silicate, 2.1 wt .-% cellulose ether, 8.8 wt. % of the di-n-nonyl ether obtained in Example 1 and water are mixed to form an aqueous slurry which has been spray-dried with superheated steam according to the method of European Patent EP-A-0 625 922.
- a conventional lime mud was prepared from 7.6 g prehydrated bentonite, 1.15 g ferrochromolignosulfonate, 2.3 g slaked lime, 0.38 g starch and 0.76 g NaOH. 5% by weight of the nonyldiethylene glycol 1-ethers obtained in Example 2 were added to this lime rinse.
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Abstract
L'invention concerne un procédé de fabrication d'une composition organique qui contient un composant fonctionnel sélectionné dans le groupe constitué d'un polymère thermoplastique, d'une enzyme, d'un liant, d'une paraffine, d'une huile, d'un colorant et d'une substance de soin pour les cheveux ou pour la peau, le procédé comprenant les étapes suivantes : i) fourniture ia) d'un n-nonyléther comme additif, qui peut être obtenu par réaction d'un composant de n-nonylalcool avec un autre composant capable de réagir avec le composant de n-nonylalcool en formant un n-nonyléther, ib) du composant fonctionnel, et éventuellement ic) d'au moins un autre additif; ii) mélangeage du n-nonyléther, du composant fonctionnel et le cas échéant du ou des autres additifs. L'invention concerne en outre : un procédé de fabrication d'un corps moulé, un procédé de fabrication d'un produit d'emballage, l'utilisation d'au moins un n-nonyléther, l'utilisation d'un corps moulé, un procédé de nettoyage des surfaces de trous forés, de dispositifs de forage ou de menu de forage, des procédés de réalisation d'un trou foré et des procédés de fabrication d'une huile ou d'un gaz.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102007055594A DE102007055594A1 (de) | 2007-11-20 | 2007-11-20 | Verfahren zur Herstellung einer organischen Zusammensetzung beinhaltend einen N-Nonylether |
DE200810009368 DE102008009368A1 (de) | 2008-02-14 | 2008-02-14 | Verfahren zur Herstellung einer organischen Zusammensetzung beinhaltend einen N-Nonylether |
PCT/EP2008/065938 WO2009065906A2 (fr) | 2007-11-20 | 2008-11-20 | Procédé de fabrication d'une composition organique contenant un n-nonyléther |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2215200A2 true EP2215200A2 (fr) | 2010-08-11 |
Family
ID=40639762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08852039A Withdrawn EP2215200A2 (fr) | 2007-11-20 | 2008-11-20 | Procédé de fabrication d'une composition organique contenant un n-nonyléther |
Country Status (3)
Country | Link |
---|---|
US (1) | US20100300694A1 (fr) |
EP (1) | EP2215200A2 (fr) |
WO (1) | WO2009065906A2 (fr) |
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WO2009065903A2 (fr) * | 2007-11-20 | 2009-05-28 | Cognis Oleochemicals Gmbh | Procédé de production d'une composition organique comprenant un n-nonylester |
DE102008044706A1 (de) * | 2008-08-28 | 2010-03-04 | Emery Oleochemicals Gmbh | Viskositätsreduzierer für Polyetherpolyole |
US20120322694A1 (en) * | 2010-06-28 | 2012-12-20 | Baker Hughes Incorporated | Electrically Conductive Oil-Base Fluids for Oil and Gas Applications |
US20120245058A1 (en) * | 2011-03-22 | 2012-09-27 | Baker Hughes Incorporated | Graphene-Containing Fluids for Oil and Gas Exploration and Production |
EP3680246A1 (fr) * | 2011-05-10 | 2020-07-15 | Archer Daniels Midland Company | Dispersants dotés de composés d'origine biologique |
CN103614130A (zh) * | 2013-12-04 | 2014-03-05 | 北京安镁瑞普环保技术开发有限公司 | 生物酶制剂 |
CN103725266A (zh) * | 2013-12-23 | 2014-04-16 | 河南海洋化工有限公司 | 钻井液用防塌抑制剂及其制备方法 |
US10737480B2 (en) | 2014-07-08 | 2020-08-11 | Amril Ag | Sinterable feedstock for use in 3D printing devices |
WO2016118146A1 (fr) * | 2015-01-22 | 2016-07-28 | Halliburton Energy Services, Inc. | Composition de ciment compatibilisée pour le traitement d'une formation souterraine |
US10662364B2 (en) * | 2015-03-20 | 2020-05-26 | Resinate Materials Group, Inc. | Drilling fluids containing polyester polyols |
US10173943B2 (en) | 2015-05-11 | 2019-01-08 | Dow Agrosciences, Llc | Non-corrosive nitrification inhibitor polar solvent formulation |
WO2017069827A1 (fr) * | 2015-10-22 | 2017-04-27 | Dow Agrosciences, Llc | Formulation à base de solvant polaire d'inhibiteur de nitrification non corrosif |
US11905492B2 (en) * | 2020-02-21 | 2024-02-20 | Illinois Tool Works Inc. | Odor removing composition comprising zinc ricinoleate and fluorosurfactant and methods of making thereof |
CN112574724A (zh) * | 2020-12-10 | 2021-03-30 | 中油昆仑管道工程有限公司 | 用于定向钻穿越黏土层的泥浆 |
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- 2008-11-20 WO PCT/EP2008/065938 patent/WO2009065906A2/fr active Application Filing
- 2008-11-20 EP EP08852039A patent/EP2215200A2/fr not_active Withdrawn
- 2008-11-20 US US12/743,850 patent/US20100300694A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
---|---|
WO2009065906A3 (fr) | 2009-08-13 |
US20100300694A1 (en) | 2010-12-02 |
WO2009065906A2 (fr) | 2009-05-28 |
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