WO2006092272A2 - Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung - Google Patents
Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung Download PDFInfo
- Publication number
- WO2006092272A2 WO2006092272A2 PCT/EP2006/001831 EP2006001831W WO2006092272A2 WO 2006092272 A2 WO2006092272 A2 WO 2006092272A2 EP 2006001831 W EP2006001831 W EP 2006001831W WO 2006092272 A2 WO2006092272 A2 WO 2006092272A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- acrylic acid
- water
- dehydration
- phase
- gas
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/52—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition by dehydration and rearrangement involving two hydroxy groups in the same molecule
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
- B01J8/0242—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid flow within the bed being predominantly vertical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/00106—Controlling the temperature by indirect heat exchange
- B01J2208/00168—Controlling the temperature by indirect heat exchange with heat exchange elements outside the bed of solid particles
- B01J2208/00212—Plates; Jackets; Cylinders
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00017—Controlling the temperature
- B01J2208/0053—Controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00002—Chemical plants
- B01J2219/00004—Scale aspects
- B01J2219/00006—Large-scale industrial plants
Definitions
- the present invention relates to a process for the production of acrylic acid, a process for the preparation of polymers by radical polymerization of acrylic acid, preferably for the preparation of water-absorbing polymers, the water-absorbing polymers obtainable by this process, water-absorbing polymers containing at least 25 wt .-% of partially neutralized Acrylic acid, a composite, a process for producing a composite, the composite obtainable by this process, the use of acrylic acid for producing water-absorbing polymer structures, an apparatus for producing acrylic acid, a process for producing acrylic acid and the acrylic acid obtainable by this process.
- a high content of acrylic acid dimers or acrylic acid oligomers is disadvantageous since these dimers or oligomers are incorporated into the polymer backbone in the preparation of superabsorbents by radical polymerization of acrylic acid in the presence of crosslinking agents.
- the copolymerized dimers are split to form ⁇ -hydroxypropionic acid, which is dehydrated under the postcrosslinking conditions to form acrylic acid.
- a high content of dimeric acrylic acid in the acrylic acid used for the preparation of the superabsorbent therefore leads to the content of acrylic acid monomers in a thermal treatment of the polymers, such as occurs in the post-crosslinking, increases.
- the soluble components in particular the acrylic acid monomers in the superabsorbent polymers, can cause skin irritation, the use of these polymers in hygiene articles requires a particularly low content of extractables.
- Acrylic acid prepared conventionally from propylene contains not insignificant amounts of double bond ketones, especially protoanemonin (PTA). This compound, upon contact with the skin, can cause symptoms of intoxication, such as redness, itching or blistering.
- Acrylic acid-based superabsorbents which contain high amounts of PTA as soluble constituents, are therefore of concern from a dermatological point of view.
- PTA interferes with the polymerization, as described, for example, in US-A-2002/0120085.
- DE-A-101 38 150 proposes to reduce the aldehyde content in the acrylic acid by bringing it into contact with an aldehyde scavenger in order to convert the aldehydes into high-boiling compounds which can then be separated off by distillation.
- Non-removed reagents are included in the superabsorbent obtained from such acrylic acid as soluble components which may come into contact with the skin of the sanitary article carrier when using the superabsorbents in sanitary articles. Furthermore, with the methods known from the prior art for the removal of aldehydes and ketones from acrylic acid, these impurities can only rarely be completely removed. In addition, such additives may adversely affect the polymerization and thus the properties of the resulting polymer.
- the object of the present invention was to provide polymers, in particular superabsorbents, which have a particularly low content of extractable, optionally toxic constituents.
- a further object of the present invention was to provide polymers, in particular superabsorbents, which are environmentally compatible and nevertheless have outstanding application properties. In particular, it was necessary to create superabsorbents with improved environmental compatibility and consistently good absorber properties.
- an object of the present invention was to propose a method and a device for producing the monomers or the polymers. conditions which can be integrated into existing large-scale production processes and devices with the least possible conversion effort.
- a contribution to achieving the abovementioned objects is made by a process for the production of acrylic acid, comprising at least the following steps: a. Dehydrating glycerine to an acrolein-containing dehydration product; b. Gas-phase oxidation of the dehydration product to give an acrylic acid-having monomer gas; c. contacting the monomer gas with a quenching agent to obtain an acrylic acid-containing quenching phase; d. Working up of the quench phase to obtain an acrylic acid-containing monomer phase.
- a further contribution to achieving the above objects is provided by a process for the preparation of a polymer by radical polymerization of acrylic acid, comprising at least the following steps:
- the glycerol is obtained from the saponification of fats.
- These fats can be both animal and vegetable fats. Animal fats are particularly important in carcass utilization. Vegetable fats fall in major shortfalls in oil production from oil crops such as oilseed rape, soy, sesame, olives and sunflower seeds. Large amounts of glycerol are particularly incurred in the production of so-called "biodiesel" from rapeseed oil, as can be seen inter alia from WO-A-2004 / 029016. Accordingly, it is preferred in the process according to the invention that the glycerol is used in the production of liquid fuels from natural raw materials, which is particularly present in oil mills downstream saponification facilities.
- the dehydration takes place at least partially in the liquid phase.
- liquid phases in particular aqueous systems are preferred. If the dehydration is carried out at least partially or even completely in a liquid phase, this has the advantage, in particular if this is an aqueous phase, that at high glycerol concentrations high acrolein concentrations in the aqueous phase can be achieved.
- aqueous phases with high acrolein concentrations can be used directly in the next step of gas phase oxidation.
- the aglolein-related excipients are separated off and the acrolein is fed to the gas-phase oxidation. So much longer catalyst life can be achieved.
- Another advantage of the liquid phase dehydration is that a rinsing effect can be achieved by the liquid phase, with the formation of a deposit on a solid catalyst can be significantly reduced, which leads to higher catalyst run times and thus to a lower regeneration requirement of the catalyst.
- a further advantage of the liquid phase dehydration is that they are carried out at relatively moderate temperatures, in a range from 160 to 270 ° C., preferably in a range from 180 to 260 ° C. and moreover preferably in a range from 215 to 245 ° C. can.
- the temperatures are in a range of 170 to 290 ° C, preferably in a range of 190 to 289 ° C, and more preferably in a range of 225 to 288 ° C.
- liquid phase dehydration it is preferred that this be done in a recycle mode in which, in the case of a solid catalyst, the glycerine-containing liquid phase is passed through a pump over the catalyst in a charge system.
- liquid catalysis or homogeneous catalysis at least one partial stream from the reactor is circulated. Reacted glycerol, spent catalyst and possibly withdrawn water are preferably added to the sub-stream fed back into the reactor in the recycle mode at the reactor inlet. If the partial stream is obtained during an acidically catalyzed dehydration, it is advantageous that the partial stream is at least partially neutralized. By this measure, the formation of by-products can be inhibited by reactions in the partial flow or even prevented.
- high boilers substances it is advantageous to deplete of the partial stream higher than acrolein boiling, referred to as high boilers substances. This can be done, for example, by membranes, which are preferably semipermeable, having separation units. Thus, in addition to a high selectivity, higher conversions and significantly fewer by-products can be obtained in a gentle way.
- this liquid glycerol phase generally has a water content in a range of 0 to 97 wt .-%, for example 0 to 30 wt.%, Preferably in a range of 60 to 95 wt .-%, particularly preferably in a range of 70 to 90 wt .-%, but also a smaller water content, for example, a water content in a range of 0 to 20 wt.% Or from 0 to 10 wt.% Water, each based on the aqueous phase, conceivable is.
- the aqueous glycerin phase generally has an amount of water in the range of 0 to 97% by weight, preferably in a range of 60 to 95% by weight, and more preferably in a range of 70 to 90% by weight, respectively based on the aqueous glycerol phase, wherein it may be particularly advantageous here to use smaller amounts of water, for example a water content in a range from 0 to 20% by weight or from about 0 to 10% by weight.
- the other main constituent of the glycerol phase is glycerol. Further advantages of gas phase dehydration are high conversions up to a total conversion with equally high space-time yields.
- the glycerol can first be supplied to the gas phase dehydration and then to the liquid phase dehydration or in reverse order.
- the former sequence there is the advantage that saline-laden glycerol batches originating from the fat saponification can be prepared by vaporization in the gas phase dehydration of this salt freight and then further increased to high yields and selectivities with few Ne in liquid phase dehydration by the recycle mode - Ben arean be implemented.
- a dehydration catalyst is used in this.
- Suitable dehydration catalysts are both acidic and alkaline catalysts. Acid catalysts are particularly preferred because of the low tendency toward oligomer formation.
- the dehydration catalyst can be used both as a homogeneous and as a heterogeneous catalyst. When the dehydration catalyst is a heterogeneous catalyst, it is preferred that the dehydration catalyst be supported by a carrier x. in contact. As a carrier x. all suitable to the expert appear suitable solids into consideration. In this context, it is preferred that these solids have suitable pore volumes which are suitable for good binding and absorption of the dehydration catalyst.
- total pore volumes according to DIN 66133 in a range of 0.01 to 3 ml / g are preferred and in a range of 0.1 to 1.5 ml / g particularly preferred.
- the carrier x. suitable solids have a surface area in the range of 0.001 to 1000 m 2 / g, preferably in the range of 0.005 to 450 m 2 / g and more preferably in the range of 0.01 to 300 m 2 / g according to BET test according to DIN 66131
- the carrier for the dehydration catalyst may on the one hand be a bulk material having an average particle diameter in the range from 0.1 to 40 mm, preferably in the range from 1 to 10 mm and moreover preferably in the range from 1.5 to 5 mm, be used.
- the wall of the dehydration reactor can serve as a carrier.
- the carrier per se may be acidic or basic, or an acidic or basic dehydration catalyst may be applied to an inert carrier. Dipping or impregnating or incorporation into a carrier matrix should be mentioned in particular as application techniques.
- Suitable carriers x. which may also have dehydration catalyst properties, are in particular natural or synthetic silicatic substances, in particular mordenite, montmorillonite, acidic zeolites; treated with mono-, di- or polybasic inorganic acids, in particular phosphoric acid, or acidic salts of inorganic acids, such as oxidic see or silicate substances, for example Al 2 O 3 , TiO 2 ; Oxides and mixed oxides, such as gamma-Al 2 ⁇ 3 and ZnO-Al 2 O 3 - and Cu-Al mixed oxides of heteropolyacids.
- the carrier x. at least partially consists of an oxide compound.
- Such oxidic compounds should have at least one of Si, Ti, Zr, Al, P or a combination of at least two of them.
- Such carriers can also act as dehydration catalysts themselves by virtue of their acidic or basic properties.
- a preferred both as a carrier as x. as well as acting as dehydration catalyst class of compounds include silicon, aluminum and / or phosphorus oxides.
- Preferred basic both as dehydration catalyst and as carrier x.
- Fungents include alkali, alkaline earth, lanthanum, lanthanides, or a combination of at least two of them in their oxidic form.
- Such acidic or basic dehydration catalysts are commercially available both from Degussa AG and from Südchemie AG. Another class are ion exchangers. These can also be present in both basic and acidic form.
- Suitable homogeneous dehydration catalysts are, in particular, inorganic acids, preferably phosphorous-containing acids and, moreover, preferably phosphoric acid. These inorganic acids may be on the carrier x. be immobilized by immersion or impregnation.
- heterogeneous catalysts Especially in the gas phase dehydration, the use of heterogeneous catalysts has proven particularly useful. In liquid phase dehydration, however, both homogeneous and heterogeneous dehydration catalysts are used.
- the dehydration catalyst is an inorganic acid.
- the term "acid” in this text refers to the substances that are in accordance with the definition of Brönsted as acid behavior. All acids which are known and suitable for the person skilled in the art come into consideration here. Preferably, S- and P-containing acids are mentioned, with the P-containing acids being preferred. In connection with the liquid phase dehydration, it is furthermore preferred that this is also present in a solution as a homogeneous dehydration catalyst. This solution is preferably the aqueous glycerol-containing phase used for dehydration.
- These homogeneous catalysts are contained in an amount in a range of 0.0001 to 20% by weight, preferably in a range of 0.001 to 15% by weight, and more preferably in a range of 0.01 to 10% by weight. , in each case based on the dehydrating phase used.
- a dehydration catalyst having a Ho value in the range of +1 to -10, preferably in a range of +2 to -8.2 and more preferably in the liquid phase dehydration in a range from +2 to -3 and in the gas phase dehydration in a range of -3 to -8.2.
- the Ho value corresponds to the acid function according to Hammett and can be determined by the so-called aminotration and use of indicators or by absorption of a gaseous base - see "Studies in Surface Science and Catalytics", vol. 51, 1989: Solid Acids and Bases, their catalytic properties ", K. Tannabe et al. Further details on the preparation of acrolein from glycerol can be found in DE 42 38 493 C1.
- the gas phase oxidation in step b) of the process according to the invention is carried out in the presence of one or more oxidation catalysts which have transition metals in elemental or in chemically bonded form or both.
- the oxidation catalysts it is preferred that these have at least one of the elements molybdenum, tungsten, vanadium or a combination of at least two thereof in at least partially oxidic form.
- Such oxidation catalysts are preferably used as heterogeneous catalysts with a carrier y. in Contact used standing. It is preferred that the oxidation catalysts in this carrier y. are incorporated.
- a suitable carrier y. basically come in connection with the carriers x.
- oxidation catalysts are described in detail in the literature. Reference is made by way of example to DE-A-2626 887, EP-AO 534294 and US-A-2002/0198406. Such oxidation catalysts for the conversion of acrolein to acrylic acid are commercially available, for example, from the Mitsubishi KIC.
- the dehydration product if appropriate in an aqueous phase, is fed to the gas phase oxidation.
- the dehydration product has at least 10% by weight, preferably at least 20% by weight and furthermore preferably at least 40% by weight of acrolein.
- the amount of water should be in the range of 0.001 to 50% by weight, preferably in the range of 0.1 to 50% by weight, more preferably in the range of 10 to 40% by weight and more preferably in the range of 12 to 20% by weight. %, these referring to the above wt.% data respectively relating to the phase fed into the gas phase oxidation.
- a further embodiment of the method according to the invention provides that glycerol is used as the aqueous glycerol phase having a glycerol concentration in a range from 0.1 to 90, preferably in a range from 1 to 80 and particularly preferably in a range from 2 to 50% by weight.
- % in each case based on the aqueous glycerol phase, is introduced into a dehydration space.
- This dehydration space includes both a liquid phase and a gas phase, wherein the concentration of glycerol in the liquid phase is greater than in the gas phase and wherein the concentration of acrolein in the gas phase is greater than in the liquid phase.
- the concentration of glycerol in the liquid phase is at least a factor of 1.1, preferably at least a factor of 2, and more preferably at least a factor of 5 higher than in the Gas phase.
- the concentration of the acrolein in the gas phase is at least a factor of 1.1, preferably at least a factor of 2, and more preferably a factor of 5 higher than in the liquid phase.
- the acrolein contained in the gas phase is removed from the dehydration space, which is preferably designed as a pressure reactor.
- more dehydration of glycerol into acrolein takes place in the liquid phase than in the gas phase.
- the dehydration of glycerol to acrolein is preferably carried out in the liquid phase at least by a factor of 1.1, particularly preferably by at least a factor of 2, and moreover preferably by at least a factor of 5, more than in the gas phase. It is further preferred in this embodiment that the acrolein formed in the liquid phase is converted into the gas phase. It is further preferred in this embodiment that the volume fraction of the dehydration space occupied by the liquid phase is greater than the volume fraction occupied by the gas phase.
- the volume fraction occupied by the liquid phase is preferably at least a factor of 1.1, preferably at least a factor of 2 and particularly preferably at least a factor of 5 greater than the volume fraction of the dehydration charge occupied by the gas phase.
- the factors used here can be determined, for example, on the basis of examination of the phase equilibria.
- This embodiment of the process according to the invention for the production of acrylic acid preferably comprises the following process steps: a. Dehydration of glycerin in the form of an aqueous glycerol solution to an acrolein dehydration product in the form of an aqueous acrolein solution by liquid phase dehydration with at least partial transfer of the aqueous acrolein solution to the gas phase, wherein the weight ratio of acrolein to glycerol in the gas phase by a factor of at least 2, preferably at least 4, more preferably at least 10 and most preferably at least 100 greater is the weight ratio of acrolein to glycerol in the aqueous
- the process for producing a polymer in this particular embodiment of the process according to the invention comprises the following process steps:
- the gas-phase oxidation is preferably carried out in a temperature range of 200 to 400 0 C, preferably in the range of 250 to 350 ° C and more preferably in a range from 280 to 340 ° C.
- the monomer gas contains the acrylic acid in an amount in the range of 5 to 50% by weight, preferably in the range of 10 to 40% by weight, and more preferably in the range of 15 to 15% 30% by weight, based in each case on the monomer gas.
- quenching agent in process step c) of the process according to the invention water or an organic compound having a boiling point in the range of 50 to 250 0 C, preferably in a range of 70 to 18O 0 C and beyond preferably in a range of 105 to 150 0 C or water and to use this organic compound.
- Aromatics and, moreover, preferably alkylated aromatics may be considered as such an organic compound.
- the quenching agent is contacted with the monomer gas in a suitable column, preferably in countercurrent.
- the acrylic acid-laden aqueous quenching agent in a further step with a release agent, preferably not good with water is soluble, is worked up.
- the acrylic acid-rich phase is subjected to either a distillation or a crystallization or both, preferably first a crystallization.
- the crystallization can be carried out both as a layer and as a suspension crystallization.
- Suitable layer crystallization devices are commercially available from Sulzer AG.
- Suitable suspension crystallization processes usually make use of a crystal generator followed by a wash column. Such devices and methods are commercially available from Niro Listetechnologie BV.
- extraction / release agent is in particular an aromatic compound, moreover preferably an alkylaromatic and further preferably toluene into consideration.
- an organic compound be used as a release agent, this charged with acrylic acid organic compound also both a distillation and a crystallization or a Combination of both.
- a crystallization suitable for this purpose is disclosed in EP-A1 015 410.
- the quenching phase contains the acrylic acid in an amount in the range of 30 to 90% by weight, preferably in the range of 35 to 85% by weight, and more preferably in the range of 45 to 75% by weight %, in each case based on the monomer phase.
- the work-up of the quench phase takes place at temperatures below the boiling point of the acrylic acid.
- the quench comprises using a correspondingly cold quench already a temperature of below 4O 0 C.
- the so-tempered quenched phase can be then supplied to an extraction or crystallization, or both, for working up, the temperatures are preferably in a range from - 40 till 40 0 C, preferably in a range of -20 to 39 ° C and particularly preferably in a range of -10 to 35 ° C lie.
- the monomer phase contains the acrylic acid in an amount in the range from 99 to 99.98% by weight, based in each case on the monomer phase.
- acrylic acid contents in a monomer phase occur in particular when working up takes place by distillation.
- the acrylic acid is contained in an amount of 30 to 70% by weight, preferably in an amount of 40 to 60% by weight and more preferably in an amount in a range from 45 to 65% by weight in the monomer phase in addition to water, and the impurities other than water and acrylic acid are less than 0.02% by weight, based on the monomer phase.
- This aqueous monomer phase has the advantage that it can be used without further dilution. step, which is necessary in the highly concentrated monomer phase, can be used in the aqueous polymerization of the monomer phase.
- the invention relates to a device for the production of acrylic acid, the fluid-conducting connected to each other comprising the following components:
- Ia a dehydration reactor
- 2a a gas phase oxidation reactor
- 3 a a quenching unit
- 4a a workup unit.
- the invention relates to a device for the preparation of polymers, the fluid-conducting interconnected first, the components listed above Ia. to 4a. and further, a polymerization unit 5b. having.
- the dehydration reactor has a starting material container suitable for the absorption of glycerol, followed by a reaction area configured to receive catalyst, again followed by a quencher with a discharge to the gas phase oxidation reactor.
- a starting material container suitable for the absorption of glycerol
- a reaction area configured to receive catalyst
- a quencher with a discharge to the gas phase oxidation reactor are formed from conventional materials used in the chemical industry, inert to the reaction conditions, such as stainless steel or glass.
- the reaction region may also have walls that act as a catalyst.
- the quencher is designed as a column into which water or high-boiling organic solvent can be fed.
- a further development of the device according to the invention has, after the educt container and before the reaction zone, an evaporator. These embodiments are particularly suitable for gas phase dehydration.
- the glycerin is used from the fatty acid saponification with a high salt load, it is preferable that the evaporator has
- the reaction region has a lower product outlet, which opens into the quencher.
- This construction method has proven particularly in connection with the gas phase dehydration.
- the reaction region has an upper product outlet which opens into the quencher. This type of construction has proven particularly successful in liquid phase dehydration.
- the reaction zone is incorporated in a circuit with which reactants and reaction product can be circulated.
- Suitable gas-phase oxidation reactors are all reactors which are familiar to the person skilled in the art and appear suitable for the process according to the invention and which are capable of reacting acrolein by gas-phase oxidation to give acrylic acid.
- a coolant preferably a molten salt.
- These tube bundle or plate reactors take on the side facing away from the coolant to a suitable catalyst. This can on the one hand be present as a powder bed and on the other hand, the surfaces of the tubes or the plates may be coated with the catalyst.
- quenching units the types commonly used in the previous large-scale gas phase oxidation of acrolein to acrylic acid are also preferably used.
- Such Quenchüen are designed as columns or towers and can as well as the reactors, for example, from the Deggendorfer shipyard GmbH be acquired commercially.
- Also suitable as a work-up unit are all the distillation and crystallization and extraction devices known to the person skilled in the art from the large-scale synthesis of acrylic acid by gas phase oxidation of acolein.
- Suitable polymerization units which are used in process step E. for the polymerization of the monomer phase, on the one hand discontinuously operating stirred tank and on the other hand continuously operating systems, such as belt polymerization, extruder and the like are suitable. These polymerization reactors are followed by comminution and drying. The superabsorber precursor thus obtained can be further subjected to surface or postcrosslinking.
- surface or postcrosslinking please refer to the aforementioned work by Graham & Buchholz. If the polymers are cross-linked, partially neutralized polyacrylates, the exact procedure is referred to the 3rd chapter (page 69ff) in "Modern Superabsorbent Polymer Technology", FL Buchholz and AT Graham (publisher) in VCH, New York, 1998, which forms part of this disclosure.
- water-absorbing polymer structures can be obtained as particularly suitable superabsorbers.
- a contribution to the solution of the abovementioned objects is also afforded by water-absorbing polymer structures obtainable by free-radical polymerization of the acrylic acid obtainable by the above-described synthesis process in the presence of crosslinking agents.
- Water-absorbing polymer structures which contribute at least 25% by weight, preferably at least 50% by weight, more preferably at least 75% by weight and most preferably at least 95% by weight, also contribute to the solution of the abovementioned objects.
- non-fossil, renewable organic material emanates.
- non-fossil, renewable organic materials are, in particular, not materials derived from petroleum, or from coal or lignite, and from natural gas. Rather, these non-fossil, renewable organic materials are products of agriculture and forestry, especially fats and oils of glycerol and fatty acids.
- these water-absorbing polymer structures are obtainable by a process comprising the following process steps: i) polymerization of the acrylic acid in the presence of a crosslinker to form a polymer gel; ii) optionally comminution of the polymer gel; iii) drying of the optionally comminuted polymer gel to obtain water-absorbing polymer structures, and iv) optionally surface post-treatment of the water-absorbing polymer structures.
- inventive water-absorbing polymer structures these are based on at least 25% by weight, preferably at least 35% by weight and most preferably at least 45% by weight of natural, biodegradable polymers, preferably on carbohydrates such as cellulose or strength.
- Polymeric structures preferred according to the invention are fibers, foams or particles, with fibers and particles being preferred and particles being particularly preferred.
- polymer fibers are dimensioned so that they can be incorporated into or as yarn for textiles and also directly in textiles. It is inventively preferred that the polymer fibers have a length in the range of 1 to 500, preferably 2 to 500 and more preferably 5 to 100 mm and a diameter in the range of 1 to 200, preferably 3 to 100 and particularly preferably 5 to 60 denier ,
- Polymer particles preferred according to the invention are dimensioned such that they have an average particle size according to ERT 420.2-02 in the range from 10 to 3000 ⁇ m, preferably 20 to 2000 ⁇ m and particularly preferably 150 to 850 ⁇ m. Furthermore, it is preferred that the proportion of particles having a particle size in a range from 300 to 600 ⁇ m is at least 50% by weight, particularly preferably at least 75% by weight.
- CRC Centrifugation Retention Capacity
- ERT Edana Recommended Test Method
- the polymer structure is based on at least 25 wt .-%, preferably at least 50 wt .-%, more preferably at least 75 wt .-% and most preferably at least 95 wt .-%, of acrylic acid, wherein at least 80 wt .-%, preferably at least 90 wt .-% and most preferably at least 95 wt.% Of the acrylic acid monomers used for the preparation of the water-absorbing polymer structures by a
- the polymer structure has a biodegradability determined according to the modified Sturm test according to Annex V to Directive 67/548 / EEC after 28 days of at least 25%, preferably at least 35% and most preferably at least 45%, one value of maximum
- the polymer structure has a CRC value determined according to ERT 441.2-02 of at least 20 g / g, preferably at least 25 g / g and most preferably at least 29 g / g, a CRC value of 60 g / g , as upper limit in general is not exceeded.
- this has at least the properties ßl and ß2. All further developments specified in this text for the polymer structures also apply to the polymer structure of this paragraph.
- water-absorbing polymer structures which are preferred for at least 10, preferably at least 25, more preferably at least 50 and moreover at least 75 and furthermore preferably at least 80% by weight, based in each case on the polymer structure, of acrylic acid, which are characterized by the following properties:
- the polymer structure shows a sustainability factor of at least 10, preferably at least 20, more preferably at least 50, moreover preferably at least 75, further preferably at least 85 and further preferably at least 95;
- the polymer structure has a biodegradability determined according to the modified Sturm test according to Annex V to Directive 67/548 / EEC after 28 days of at least 25%, preferably at least 35% and most preferably at least 45%, one value of a maximum of 75 to 95% as upper limit in general is not exceeded;
- the polymer structure has a CRC value determined according to ERT 441.2-02 of at least 20 g / g, preferably at least 25 g / g and most preferably at least 29 g / g, a CRC value of 60 g / g , as upper limit in general is not exceeded.
- this has at least the properties ⁇ l and ⁇ 2. All further developments specified in this text for the polymer structures also apply to the polymer structure of this paragraph.
- the above upper limits may also be up to 10% or even up to 20% lower.
- these di- or polysaccharides are preferably in an amount of at least 1 wt .-%, preferably at least 5 wt .-% and more preferably at least 15 wt .-%, each based on the polymer structure, as another Component of the polymer structure, so that the sum of the wt .-% of the components of the water-absorbing polymer structure 100 wt .-% results.
- chain polyoxides are preferred which preferably have a number average molecular weight in the range of 10,000 to 1,000,000, and preferably in the range of 50,000 to 500,000 g / mol, as determined by gel permeation chromatography and light scattering. These are preferably made of linear and thus unmistakable chains.
- suitable sugar compounds are all known to those skilled and suitable appearing suitable sugar compounds into consideration.
- cellulose and starch may be mentioned, with one or at least two different starches being preferred.
- amylose-containing starches are preferred.
- the amylose content is preferably in a range of 10 to 80, and more preferably in a range of 20 to 70 wt .-%, each based on the starch.
- the di- or polysaccharides have a particle size in which at least 50% by weight, preferably at least 70% by weight and moreover preferably at least 85% by weight of the particles are smaller than 50 ⁇ m.
- the particle size is determined by sieve analysis.
- Such products are, for example, under the brand Eurylon ® 7 or Foralys ® 380 Roquette - France - commercially available.
- the water-absorbing polymer is at least 50 wt .-%, preferably at least 80 wt .-% and more preferably at least 95 wt .-% based on acrylic acid derived from the dehydration process according to the invention and partially neutralized with a crosslinking agent for Polymerization is used.
- the surface networking is through here achieved post-crosslinking already achieved.
- the sustainability factor indicates to what proportion the polymer structure is based on substances based on non-fossil, renewable organic material. At a sustainability factor of 100, the polymer structure consists entirely of non-fossil, renewable organic materials.
- a further solution to the problems described at the outset is a composite comprising the inventive water-absorbing polymer structures or water-absorbing polymer structures obtainable by free-radical polymerization of the acrylic acid obtainable by the above-described synthesis process in the presence of crosslinking agents.
- the polymer structures according to the invention and the substrate are firmly connected to one another.
- films of polymers such as polyethylene, polypropylene or polyamide, metals, nonwovens, threads, tissues, fabrics, natural or synthetic fibers, or other foams are preferred.
- the polymer structures it is preferred according to the invention for the polymer structures to be present in an amount of at least 50% by weight, preferably at least 70% by weight and even more preferably at least 90% by weight, based on the total weight of polymer structure and substrate in the composite are included.
- the composite according to the invention is a sheet-like composite, as described in WO-A-02/056 812 as "absorbent material.”
- absorbent material a sheet-like composite, as described in WO-A-02/056 812 as "absorbent material.”
- a further contribution to the solution of the abovementioned objects is provided by a method for producing a composite, wherein the present invention water-absorbing polymers which are obtainable by radical polymerization of the acrylic acid obtainable by the synthesis process described above in the presence of crosslinking agents, and a substrate and optionally an additive are brought into contact with each other.
- the substrates used are preferably those substrates which have already been mentioned above in connection with the composite according to the invention.
- chemical products comprising the water-absorbing polymer structures according to the invention or a composite according to the invention.
- Preferred chemical products are, in particular, foams, moldings, fibers, films, cables, sealing materials, liquid-absorbent hygiene articles, in particular diapers and sanitary napkins, carriers for plant or fungi growth-regulating agents or crop protection active ingredients, additives for building materials, packaging materials or floor additives.
- Preferred chemical products are sanitary articles comprising an upper layer, a lower layer and an intermediate layer between the upper layer and the lower layer, which contains water-absorbing polymer structures according to the invention.
- the invention relates to a process for the production of acrolein characterized by the process described herein for the dehydration of glycerol to an acrolein-containing dehydration product and the preferred embodiments of this dehydration described herein.
- the invention further relates to fibers, films, adhesives, cosmetics, molding compositions, textile and leather auxiliaries, flocculants, coatings or lacquers based on acrylic acid, obtainable by a process according to the invention is, or their derivatives or salts.
- Suitable derivatives of acrylic acid are in particular their esters, preferably their alkyl esters and moreover preferably their C 1 to C 10 , more preferably C 2 to C 5 and further preferably C 3 to C 4 alkyl esters.
- Salts are the alkali metal or alkaline earth metal salts and the ammonium salts of acrylic acid.
- the invention further relates to the use of an acrylic acid obtained by a process according to the invention or its derivatives or salts in fibers, films, adhesives, cosmetics, molding compositions, textile and leather auxiliaries, flocculants, coatings or paints.
- FIG. 1 shows a schematic sequence of the individual steps and steps of the method according to the invention and the device according to the invention.
- Fig. 2 shows a gas phase dehydration unit.
- Fig. 3 shows a liquid phase dehydration unit.
- Fig. 4 shows a processing unit.
- Fig. 5 shows another embodiment of the liquid phase dehydration unit
- the oils or fats are first introduced into a saponifier 1 where alkaline saponification with lyes or alkali alcoholates takes place.
- the glycerin recovered in the saponifier according to generally known purification steps such as salting-out and distillation is then fed to a dehydration unit with a dehydration reactor 2 (to recover from the glycerol acrolein).
- the acrolein thus obtained is then fed in a next step to a gas phase reactor 3 in which it is replaced by a gas phase oxidation reaction. action is converted to acrylic acid.
- the gas phase reactor 3 is followed by a quench unit 4, in which the acrylic acid-containing gas from the gas phase reactor 3 is brought into the liquid phase by bringing it into contact with a quencher.
- the liquid mixture of quenching agent and acrylic acid is fed to a processing unit 5 following the quenching unit 4.
- the acrylic acid is either by crystallization or distillation or a combination of these two steps or by extraction or a combination of extraction and crystallization or a combination of extraction and distillation or a combination of extraction distillation and distillation to pure acrylic acid (at least 99.98 % Acrylic acid) which is present either as pure acrylic acid by itself or in an aqueous phase.
- the acrylic acid thus obtained is then fed to a polymerization unit 6.
- the polymer obtained in the polymerization unit 6 can be formulated according to the following use.
- the polymerization unit 6 can be followed by a further processing unit, for example a diaper machine or a machine for the production of dressing and wound materials.
- FIG. 2 shows a gas phase dehydration unit in which a reactant container 7 is connected to an evaporator 12.
- the evaporator 12 is connected upstream of a reaction area 9.
- the pressure-resistant reaction region 9 has catalyst 8.
- Both the evaporator 12 and the reaction zone 9 have heating elements 21 with which the temperatures necessary for evaporation and dehydration of the glycerine can be set.
- Via a lower outlet 13 the reaction region 9 is connected to a quencher 10.
- the quencher 10 receives in its upper region next to the lower product outlet 13 still a Quench irregularkeitseinspeisung 16.
- a collecting container for by-products 17 follows, which can be emptied via a drain valve 19.
- the upper region of the quencher 10 also receives a discharge line 11 which supplies the acrolein-containing dehydration product to the gas phase reactor 3.
- This is followed by the quench unit 4.
- 3 shows a liquid-phase dehydration preparation in which glycerol is introduced into a starting material container 7, which is connected to the upper region of a pressure-loadable reaction region 9, which in turn comprises catalysts 8.
- the reaction area 9 is tempered by a heating element 21.
- a buffer container 18 connects, which forms a circuit 20 via a pump with the reaction region, over which already in the reaction region 9 and the buffer container 18 located glycerol and acrolein can be circulated.
- a transition line 2x1 to a quencher 10 which opens into the upper region of the quencher 10 together with a quench liquid feed 16.
- a discharge line 11 to the gas phase reaction reactor 3 which in turn is followed by the quench unit 4.
- a collecting container 17 for by-products 17 equipped with a discharge valve 19 opens.
- Fig. 4 the originating from the gas phase reaction reactor 3 gas is introduced into the quench unit 4, in which it is contacted with water and absorbed, wherein as the absorption liquid, an acrylic acid aqueous solution is obtained, in which also ent a part of the ent in the above synthetic steps - standing by-products is included.
- this aqueous acrylic acid solution is fed to an extraction unit 23.
- the acrylic acid solution is brought into contact with toluene as release agent (TM).
- TM release agent
- the substantially based on the release agent phase is fed via the feed 24 to the crystallizer 25, which is preferably a scraped-surface cooler.
- the crystal suspension obtained in the crystallizer 25 is then fed via a suspension feed 26 to a wash column 27, in which a separation of the acrylic acid crystals takes place, in the course of which a mother liquor containing the release agent is retained.
- the in the wash column 27 after the separation of the acrylic Acid crystals obtained mother liquor is preferably at least partially recycled via the mother liquor 28 into the extraction unit 23. It is further preferred that the essentially water-based upper phase obtained in the extraction unit 23 is returned to the quench unit 4 via the quench guide 29.
- Fig. 5 is shown schematically that optionally mixed in a premixer 32, via the leads A to C water, glycerol and, if necessary, catalyst, for example an inorganic acid such as phosphoric acid and fed to the formed as a stainless steel pressure reactor dehydration reactor 2.
- catalyst for example an inorganic acid such as phosphoric acid
- the dehydration of glycerol to acrolein takes place in the liquid phase.
- a soluble and thus homogeneously distributable cata- sators such as an inorganic acid
- a distillation device 33 which has a low-boiling region 34 in the upper section and a high-boiling region 35 in the lower section, the acrolein-containing phase from the dehydration being fed between the two regions 34 and 35.
- the lower than acrolein boiling components led out via discharge E and led the remaining acrolein and the high boiler in the reflux.
- the high boiler area representing the high boiler area 35 the high boiler are concentrated. In this case, it is advantageous for the sump product to be circulated. From the high boiler area, the components boiling higher than acrolein are discharged and fed to a high boiler 37 via a heavy-duty pump.
- the high-boiler separator 37 is advantageously equipped with a membrane.
- the freed from the high boilers primarily water and glycerol having mixture is supplied to the pre-mixer 32 after passing through the high boiler 37 and thus is the dehydration again available.
- the vaporized in an evaporator at 295 0 C glycerol was supported on 100 ml DIE ses catalyst in a steel pipe in the reaction region than 20 wt .-% aqueous solution with a pump with a 40 ml / h and at a temperature of 270 0 C.
- the acrolein inconvenience reaction mixture was with water as Quenchstoff brought into contact in the quencher and the resulting aqueous mixture of gas phase oxidation in a commercial reactor for gas phase senoxidation of acrolein to acrylic acid.
- Example 2 a catalyst as described in Example 1 was used for liquid phase dehydration (dashed lines), instead of the Rosentahl spheres being used on a silica support (H 0 value between 2 and 3).
- the reaction temperature was 240 ° C.
- Water was used as the quenching agent.
- a gas phase oxidation was carried out in a commercially available gas phase oxidation reactor, followed by absorption in water in a quench unit.
- the acrylic acid water mixtures obtained in Examples 1 and 2 were mixed with toluene in a glass separator funnel heated to 0 ° C. with 0.5 part of their volume. The mixture was vigorously shaken and allowed to stand for 60 minutes to allow phase separation. The two phases thus formed were separated. The toluene-containing phase is subjected to azeotropic distillation and the resulting acrylic acid is distilled again before being used for the polymerization.
- a monomer solution consisting of 280 g of the above-obtained acrylic acid, which was neutralized to 70 mol% with sodium hydroxide, 466.8 g of water, 1.4 g Polyethylene glycol-300 diacrylate and 1.68 g Allyloxypolyethylenglykolacryl Acid Tar- ester is freed from the dissolved oxygen by purging with nitrogen and cooled to the starting temperature of 4 0 C.
- Example 3 The polymer obtained in Example 3, postcrosslinked was treated with a wasserlösli- chen wheat starch (the product Foralys ® 380 Roquette, Lestrem, France) in the weight ratio polymer: starch of 4: 1 under dry conditions and then for 45 minutes in a roller mixer Type BTR 10 from Fröbel GmbH, Germany, further homogenized.
- a wasserlösli- chen wheat starch the product Foralys ® 380 Roquette, Lestrem, France
- the product exhibited biodegradability according to the modified storm test after 39 days of 39% and a CRC of 29.9 g / g.
- the sustainability factor was around 99. LIST OF REFERENCE NUMBERS
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2006800104254A CN101151237B (zh) | 2005-02-28 | 2006-02-28 | 丙烯酸、基于可再生资源的吸水聚合物结构及该结构的制造方法 |
JP2007557408A JP5554472B2 (ja) | 2005-02-28 | 2006-02-28 | アクリル酸、再生可能原料系の吸水性ポリマー構造、及び前記構造の製造方法 |
US11/817,247 US20090134357A1 (en) | 2005-02-28 | 2006-02-28 | Acrylic acid, water-absorbent polymer structures based on renewable resources and method for producing said structures |
EP06707335.3A EP1866272B1 (de) | 2005-02-28 | 2006-02-28 | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung |
BRPI0607884-2A BRPI0607884A2 (pt) | 2005-02-28 | 2006-02-28 | processos de produção de ácido acrìlico e polìmeros, dispositivos de produção de ácido acrìlico e polìmeros, estruturas poliméricas hidroabsorventes, compósito, processo de produção de compósito, produtos compreendendo ácido acrìlico, e uso de ácido acrìlico |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005009586.0 | 2005-02-28 | ||
DE102005009586 | 2005-02-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006092272A2 true WO2006092272A2 (de) | 2006-09-08 |
WO2006092272A3 WO2006092272A3 (de) | 2007-04-26 |
Family
ID=36501901
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/001831 WO2006092272A2 (de) | 2005-02-28 | 2006-02-28 | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung |
Country Status (8)
Country | Link |
---|---|
US (1) | US20090134357A1 (de) |
EP (1) | EP1866272B1 (de) |
JP (2) | JP5554472B2 (de) |
CN (1) | CN101151237B (de) |
BR (1) | BRPI0607884A2 (de) |
TW (2) | TWI438187B (de) |
WO (1) | WO2006092272A2 (de) |
ZA (1) | ZA200707214B (de) |
Cited By (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006136336A2 (de) * | 2005-06-20 | 2006-12-28 | Evonik Stockhausen Gmbh | Herstellung von acrolein, acrylsäure und wasserabsorbierenden polymergebilden aus glycerin |
WO2008007002A2 (fr) * | 2006-07-13 | 2008-01-17 | Arkema France | Catalyseur membranaire pour la synthèse d'acide acrylique à partir de glycérol |
WO2008023040A2 (de) * | 2006-08-22 | 2008-02-28 | Evonik Stockhausen Gmbh | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung mittels dehydratisierung |
WO2008053646A1 (fr) * | 2006-11-02 | 2008-05-08 | Nippon Shokubai Co., Ltd. | Procédé de fabrication d'acide acrylique, appareil de fabrication d'acide acrylique et composition pour la fabrication d'acide acrylique |
WO2008061860A1 (de) | 2006-11-20 | 2008-05-29 | Evonik Degussa Gmbh | Verfahren zur herstellung von fettsäurealkylestern und acrolein aus triglyceriden |
WO2008066082A1 (fr) | 2006-12-01 | 2008-06-05 | Nippon Shokubai Co., Ltd. | Procédé permettant de produire une composition contenant de l'acroléine et de la glycérine |
JP2008137950A (ja) * | 2006-12-01 | 2008-06-19 | Nippon Shokubai Co Ltd | グリセリンからのアクロレインの製法 |
FR2909999A1 (fr) * | 2006-12-19 | 2008-06-20 | Arkema France | Procede de preparation d'acide acrylique a partir de glycerol |
DE102007004960A1 (de) | 2007-01-26 | 2008-07-31 | Basf Se | Verfahren zur Herstellung von Acrylsäure |
JP2008174544A (ja) * | 2007-11-27 | 2008-07-31 | Nippon Shokubai Co Ltd | アクロレインの製造方法 |
DE102008040799A1 (de) | 2008-07-28 | 2008-12-11 | Basf Se | Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enthaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal |
DE102007055086A1 (de) | 2007-11-16 | 2009-05-20 | Basf Se | Verfahren zur Herstellung von Acrylsäure |
WO2009084417A1 (ja) * | 2007-12-28 | 2009-07-09 | Showa Denko K.K. | アクリル酸の製造方法 |
US7566804B2 (en) | 2007-01-26 | 2009-07-28 | Basf Aktiengesellschaft | Process for preparing acrylic acid |
DE102008001435A1 (de) | 2008-04-28 | 2009-10-29 | Basf Se | Verfahren zur Übertragung von Wärme auf eine monomere Acrylsäure, Acrylsäure-Michael-Oligomere und Acrylsäurepolymerisat gelöst enthaltende Flüssigkeit |
WO2009130915A1 (ja) * | 2008-04-25 | 2009-10-29 | 株式会社日本触媒 | ポリアクリル酸(塩)系吸水性樹脂およびその製造方法 |
EP2145872A1 (de) | 2008-07-19 | 2010-01-20 | Cognis IP Management GmbH | Verfahren zur Dehydratisierung von Alkoholen |
WO2010010309A2 (fr) * | 2008-07-25 | 2010-01-28 | Arkema France | Procede de synthese d'esters de l'acide acrylique bioressources |
DE102009027401A1 (de) | 2009-07-01 | 2010-02-18 | Basf Se | Verfahren der Abtrennung von Acrylsäure aus dem Produktgasgemisch einer heterogen katalysierten partiellen Gasphasenoxidation wenigstens einer C3-Vorläuferverbindung |
DE102008041573A1 (de) | 2008-08-26 | 2010-03-04 | Basf Se | Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enhaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal |
FR2935971A1 (fr) * | 2008-09-16 | 2010-03-19 | Arkema France | Acide bio-acrylique de grade polymere et son procede de fabrication a partir de glycerol. |
EP2186790A1 (de) * | 2007-08-29 | 2010-05-19 | Showa Denko K.K. | Verfahren zur herstellung von acrolein und verfahren zur herstellung von acrylsäure |
JP2010519191A (ja) * | 2007-02-16 | 2010-06-03 | アルケマ フランス | グリセロールからのアクリロニトリルの合成方法 |
FR2939055A1 (fr) * | 2008-12-03 | 2010-06-04 | Coatex Sas | Utilisation de polymeres acryliques dont l'acide acrylique est issu du glycerol, comme agent de dispersion ou de broyage de matieres minerales. |
DE102008060888A1 (de) | 2008-12-09 | 2010-06-10 | Evonik Stockhausen Gmbh | Verfahren zur Herstellung von Acrolein umfassend die Aufarbeitung einer Rohglycerin-Phase |
DE102008054587A1 (de) | 2008-12-12 | 2010-06-17 | Basf Se | Verfahren zur Rückspaltung von in einer Flüssigkeit F enthaltenen Michael-Addukten, die bei der Herstellung von Acrylsäure oder deren Ester gebildet wurde |
WO2010136697A1 (fr) | 2009-05-28 | 2010-12-02 | Arkema France | Polymere adhesif sensible a la pression contenant du methacrylate de tetrahydrofurfuryle |
WO2011000808A2 (de) | 2009-07-01 | 2011-01-06 | Basf Se | Verfahren der abtrennung von acrylsäure aus dem produktgasgemisch einer heterogen katalysierten partiellen gasphasenoxidation wenigstens einer c3-vorläuferverbindung |
WO2011010035A1 (fr) | 2009-07-22 | 2011-01-27 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource a partir de glycerol |
WO2011010036A1 (fr) | 2009-07-22 | 2011-01-27 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource a partir de glycerol |
DE102010001228A1 (de) | 2010-01-26 | 2011-02-17 | Basf Se | Verfahren der Abtrennung von Acrylsäure aus dem Produktgasgemisch einer heterogen katalysierten partiellen Gasphasenoxidation wenigstens einer C3-Vorläuferverbindung |
WO2011040575A1 (ja) | 2009-09-30 | 2011-04-07 | 株式会社日本触媒 | ポリアクリル酸(塩)系吸水性樹脂およびその製造方法 |
JP2011513487A (ja) * | 2008-03-13 | 2011-04-28 | フイナ・テクノロジー・インコーポレーテツド | トルエン及びメタンからのエチルベンゼンの製造方法 |
FR2953829A1 (fr) * | 2009-12-14 | 2011-06-17 | Arkema France | Procede de fabrication d'acroleine et/ou d'acide acrylique a partir de glycerol |
JP2011518111A (ja) * | 2008-04-16 | 2011-06-23 | アルケマ フランス | グリセリンからアクロレインを製造する方法 |
WO2011080447A1 (fr) | 2009-12-14 | 2011-07-07 | Arkema France | Procede de fabrication d'acroleine et/ou d'acide acrylique a partir de glycerol |
WO2011090129A1 (ja) | 2010-01-20 | 2011-07-28 | 株式会社日本触媒 | 吸水性樹脂の製造方法 |
WO2011090130A1 (ja) | 2010-01-20 | 2011-07-28 | 株式会社日本触媒 | 吸水性樹脂の製造方法 |
WO2011114051A1 (fr) * | 2010-03-18 | 2011-09-22 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource de grade polymere a partir de glycerol |
JP2011528705A (ja) * | 2008-07-22 | 2011-11-24 | アルケマ フランス | 再生可能な材料からのプロピオン酸ビニルの製造と、得られたプロピオン酸ビニルと、その使用 |
WO2012045738A1 (de) | 2010-10-08 | 2012-04-12 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
US20120100372A1 (en) * | 2010-10-23 | 2012-04-26 | Mohammad Hassan Nazaran | Chelate compounds |
US8299299B2 (en) | 2008-07-28 | 2012-10-30 | Basf Se | Process for separating acrylic acid present as a main constituent and glyoxal present as a by-product in a product gas mixture of a partial heterogeneously catalyzed gas phase oxidation of a C3 precursor compound of acrylic acid |
DE102011076931A1 (de) | 2011-06-03 | 2012-12-06 | Basf Se | Wässrige Lösung, enthaltend Acrylsäure und deren konjugierte Base |
DE102012201913A1 (de) | 2012-02-09 | 2013-08-14 | Tesa Se | Haftklebebänder auf Basis biobasierter Monomere |
US8742169B2 (en) | 2008-06-05 | 2014-06-03 | Showa Denko K.K. | Acrolein manufacturing method and acrylic acid manufacturing method |
WO2014079785A3 (de) * | 2012-11-26 | 2014-12-31 | Basf Se | Verfahren zur herstellung von superabsorbern auf basis nachwachsender rohstoffe |
DE102013226428A1 (de) | 2013-12-18 | 2015-06-18 | Basf Se | Extraktionskolonne und Verfahren zum Extrahieren eines Bestandteils aus einem Fluid |
WO2015124856A1 (fr) | 2014-02-19 | 2015-08-27 | Arkema France | Procede de production d'acide acrylique bio-source |
US9776940B2 (en) | 2015-08-07 | 2017-10-03 | Basf Se | Process for production of acrylic acid |
EP2565211B1 (de) | 2010-04-26 | 2017-10-25 | Nippon Shokubai Co., Ltd. | Polyacrylsäure(salz), wasserabsorbierendes harz auf basis von polyacrylsäure(salz) und verfahren zu seiner herstellung |
WO2020020697A1 (de) | 2018-07-26 | 2020-01-30 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
US10640588B2 (en) | 2010-04-26 | 2020-05-05 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt), polyacrylic acid (salt)-based water-absorbing resin, and process for producing same |
WO2021191042A1 (de) | 2020-03-26 | 2021-09-30 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
WO2021224044A1 (de) | 2020-05-04 | 2021-11-11 | Basf Se | Verfahren zur rückspaltung von in einer flüssigkeit f enthaltenen michael-addukten, die bei der herstellung von acrylsäure gebildet wurden |
WO2022018013A1 (en) | 2020-07-20 | 2022-01-27 | Basf Se | Aqueous polymer latex of film-forming copolymers suitable as binder in waterborne coating compositions |
WO2022034247A1 (de) | 2020-08-14 | 2022-02-17 | Tesa Se | Haftklebmasse |
DE202022101833U1 (de) | 2022-04-06 | 2022-04-25 | Basf Se | Öl-basierte Bohrflüssigkeiten mit Copolymeren aus Styrol, 2-Octylacrylat und (Meth)acrylsäure |
DE202022101834U1 (de) | 2022-04-06 | 2022-04-25 | Basf Se | Polymethylmethacrylat (PMMA) mit 2-Octylacrylat-Comonomer |
DE202022102002U1 (de) | 2022-04-13 | 2022-04-25 | Basf Se | Härtbare Zusammensetzungen enthaltend 2-Octylacrylat zur Boden- und Fahrbahnbeschichtung |
DE202022101962U1 (de) | 2022-04-12 | 2022-04-29 | Basf Se | Alkyl(meth)acrylat-Polymere enthaltend 2-Octylacrylat zur Hydrophobierung von Textilien |
WO2023006503A1 (de) | 2021-07-28 | 2023-02-02 | Basf Se | Verfahren zur herstellung von acrylsäure |
DE202023100921U1 (de) | 2023-02-27 | 2023-04-11 | Basf Se | Härtbare Zusammensetzung enthaltend 2-Octyl(meth)acrylat |
WO2023148332A1 (en) | 2022-02-04 | 2023-08-10 | Basf Se | Polymer binder based on 2-octyl acrylate, n-butyl acrylate and methyl methacrylate for aqueous coating compositions containing titanium dioxide |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7169843B2 (en) * | 2003-04-25 | 2007-01-30 | Stockhausen, Inc. | Superabsorbent polymer with high permeability |
DE10334286B4 (de) | 2003-07-25 | 2006-01-05 | Stockhausen Gmbh | Pulverförmige,wasserabsorbierende Polymere mit mittels thermoplastischen Klebstoffen gebundenen Feinteilchen, Verfahren zu deren Herstellung sowie diese beinhaltende chemische Produkte und Verbunde |
US7173086B2 (en) | 2003-10-31 | 2007-02-06 | Stockhausen, Inc. | Superabsorbent polymer with high permeability |
WO2005123781A2 (de) | 2004-06-21 | 2005-12-29 | Stockhausen Gmbh | Wasserabsorbierendes polysaccharid sowie ein verfahren zu seiner herstellung |
JP4909526B2 (ja) * | 2005-04-12 | 2012-04-04 | 花王株式会社 | アクロレインの製造方法 |
DE102005055497A1 (de) * | 2005-11-18 | 2007-05-31 | Stockhausen Gmbh | Geruchsbindende superabsorbierende Zusammensetzung |
JP5162128B2 (ja) * | 2006-12-27 | 2013-03-13 | 株式会社日本触媒 | グリセリンからのアクロレインの製造方法 |
US8236884B2 (en) | 2007-03-23 | 2012-08-07 | Evonik Stockhausen, Llc | High permeability superabsorbent polymer compositions |
US7816426B2 (en) * | 2007-07-16 | 2010-10-19 | Evonik Stockhausen, Llc | Superabsorbent polymer compositions having color stability |
DE102007045724B4 (de) | 2007-09-24 | 2012-01-26 | Evonik Stockhausen Gmbh | Superabsorbierende Zusammensetzung mit Tanninen zur Geruchskontrolle, Verfahren zu deren Herstellung und Verwendung |
US8318306B2 (en) * | 2008-01-30 | 2012-11-27 | Evonik Stockhausen, Llc | Superabsorbent polymer compositions having a triggering composition |
TWI455973B (zh) * | 2008-03-05 | 2014-10-11 | Evonik Degussa Gmbh | 用於氣味控制的具有水楊酸鋅的超吸收性組合物 |
DE102008020688B3 (de) * | 2008-04-24 | 2009-11-05 | Evonik Stockhausen Gmbh | Verfahren zur Herstellung und Aufreinigung wässriger Phasen |
JP2008280349A (ja) * | 2008-06-02 | 2008-11-20 | Nippon Shokubai Co Ltd | アクリル酸の製造方法、アクリル酸製造用装置、およびアクリル酸製造用組成物 |
JP5153462B2 (ja) * | 2008-06-05 | 2013-02-27 | 昭和電工株式会社 | アクロレインの製造方法及びアクリル酸の製造方法 |
DE102008044946B4 (de) * | 2008-08-29 | 2022-06-15 | Evonik Superabsorber Gmbh | Einsatz von Schaumkörpern in Oxidations-Reaktoren zur Herstellung ungesättigter Carbonsäuren |
US8222477B2 (en) * | 2008-10-20 | 2012-07-17 | Evonik Stockhausen, Llc | Superabsorbent polymer containing clay, particulate, and method of making same |
US7910688B2 (en) | 2008-10-22 | 2011-03-22 | Evonik Stockhausen Inc. | Recycling superabsorbent polymer fines |
EP2179981A1 (de) * | 2008-10-24 | 2010-04-28 | Arkema France | Verfahren zur Herstellung von Acrolein aus Glycerol |
US8361926B2 (en) * | 2008-11-25 | 2013-01-29 | Evonik Stockhausen, Llc | Water-absorbing polysaccharide and method for producing the same |
US8198477B2 (en) * | 2008-12-24 | 2012-06-12 | Rohm And Haas Company | Process for production of acrolein from glycerol |
EP2395029B1 (de) | 2009-02-06 | 2020-01-15 | Nippon Shokubai Co., Ltd. | Wasserabsorbierendes harz auf basis von polyacrylsäure (salz) und herstellungsverfahren dafür |
EP2371869A1 (de) | 2010-03-30 | 2011-10-05 | Evonik Stockhausen GmbH | Verfahren zur Herstellung eines hochabsorbierenden Polymers |
DE102010040921A1 (de) | 2010-09-16 | 2012-03-22 | Basf Se | Verfahren zur Herstellung von Acrylsäure aus Methanol und Essigsäure |
US8802786B2 (en) | 2011-04-21 | 2014-08-12 | Evonik Corporation | Particulate superabsorbent polymer composition having improved performance properties |
DE102013000602A1 (de) | 2013-01-16 | 2014-07-17 | Evonik Industries Ag | Verfahren zur Herstellung von Acrylsäure |
US9375507B2 (en) | 2013-04-10 | 2016-06-28 | Evonik Corporation | Particulate superabsorbent polymer composition having improved stability |
US9302248B2 (en) | 2013-04-10 | 2016-04-05 | Evonik Corporation | Particulate superabsorbent polymer composition having improved stability |
DE102013217386A1 (de) | 2013-09-02 | 2015-03-05 | Evonik Industries Ag | Verfahren zur Herstellung von Acrylsäure |
US20160194430A1 (en) * | 2013-09-06 | 2016-07-07 | Sika Technology Ag | Bio-based polycarboxylate ether and methods for the production thereof |
CN105884983A (zh) * | 2014-11-06 | 2016-08-24 | 邹城市安德机械制修有限公司 | 一种高分子吸水树脂及其制备方法 |
WO2023074720A1 (ja) * | 2021-10-27 | 2023-05-04 | 住友精化株式会社 | α,β-不飽和カルボン酸化合物の架橋重合体及びその用途 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0890591A2 (de) * | 1997-07-07 | 1999-01-13 | Idemitsu Petrochemical Co., Ltd. | Acrylatpolymer, Verfahren zu seiner Herstellung und biologisch abbaubare Builderkomponente |
US20020120085A1 (en) * | 2000-06-21 | 2002-08-29 | Nippon Shokubai Co., Ltd. | Production process for water-absorbent resin |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1916743A (en) * | 1929-06-15 | 1933-07-04 | Schering Kahlbaum Ag | Production of acrolein |
US2042224A (en) * | 1934-06-27 | 1936-05-26 | Shell Dev | Process of converting a polyhydric alcohol to a carbonyl compound |
US2558520A (en) * | 1948-01-29 | 1951-06-26 | Us Ind Chemicals Inc | Production of acrolein from glycerol |
DE2626887B2 (de) * | 1976-06-16 | 1978-06-29 | Basf Ag, 6700 Ludwigshafen | Katalysator für die Oxadation von (Methacrolein zu (Meth)Acrylsäure |
JPS55102536A (en) * | 1979-01-30 | 1980-08-05 | Mitsubishi Petrochem Co Ltd | Preparation of acrylic acid |
US5218146A (en) * | 1987-05-27 | 1993-06-08 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Process for production of acrylic acid |
JPH0686399B2 (ja) * | 1987-05-27 | 1994-11-02 | 株式会社日本触媒 | アクリル酸の製造方法 |
DE4132263A1 (de) * | 1991-09-27 | 1993-04-01 | Basf Ag | Verfahren zur katalytischen gasphasenoxidation von acrolein zu acrylsaeure |
DE4238493C1 (de) * | 1992-11-14 | 1994-04-21 | Degussa | Verfahren zur Herstellung von Acrolein und dessen Verwendung |
DE4238492C2 (de) * | 1992-11-14 | 1995-06-14 | Degussa | Verfahren zur Herstellung von 1,2- und 1,3-Propandiol |
DE19740252A1 (de) * | 1997-09-12 | 1999-03-18 | Basf Ag | Verfahren zur Herstellung von Acrylsäure und Methacrylsäure |
JPH11240959A (ja) * | 1998-02-24 | 1999-09-07 | Nippon Shokubai Co Ltd | 吸水性ポリマー組成物およびその製法 |
DE19814387A1 (de) * | 1998-03-31 | 1999-10-07 | Basf Ag | Verfahren zur Herstellung von Acrylsäure und Acrylsäureestern |
JP2000281617A (ja) * | 1999-01-29 | 2000-10-10 | Mitsubishi Chemicals Corp | アクリル酸の精製方法 |
DE60001867T2 (de) * | 1999-01-29 | 2004-01-22 | Mitsubishi Chemical Corp. | Verfahren zur Reinigung von Acrylsäure |
JP3938646B2 (ja) * | 2000-01-14 | 2007-06-27 | 株式会社日本触媒 | アクリル酸の製造方法 |
JP2001247510A (ja) * | 2000-03-08 | 2001-09-11 | Nippon Shokubai Co Ltd | アクリル酸の製造方法 |
US6441227B1 (en) * | 2000-06-23 | 2002-08-27 | Saudi Basic Industries Corporation | Two stage process for the production of unsaturated carboxylic acids by oxidation of lower unsaturated hydrocarbons |
CA2428800C (en) * | 2000-11-20 | 2011-09-13 | Dow Global Technologies Inc. | In vivo use of fluid absorbent polymers |
DE10125599A1 (de) * | 2001-05-25 | 2002-11-28 | Stockhausen Chem Fab Gmbh | Superabsorber, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE10138150A1 (de) * | 2001-08-03 | 2003-02-13 | Basf Ag | Verfahren zur Herstellung wasserabsorbierender Harze |
EP1319648B1 (de) * | 2001-12-14 | 2008-04-02 | Stockhausen GmbH | Verfahren zur Herstellung von Acrylsäure |
DE10211686A1 (de) * | 2002-03-15 | 2003-10-02 | Stockhausen Chem Fab Gmbh | (Meth)Acrylsäurekristall und Verfahren zur Herstellung und Aufreinigung von wässriger (Meth)Acrylsäure |
DE10243700A1 (de) * | 2002-09-20 | 2004-04-01 | Oelmühle Leer Connemann Gmbh & Co. | Verfahren und Vorrichtung zur Herstellung von Biodiesel |
JP2005036100A (ja) * | 2003-07-14 | 2005-02-10 | Nippon Shokubai Co Ltd | 吸水性樹脂を製造する方法 |
JP5006507B2 (ja) * | 2004-01-30 | 2012-08-22 | 株式会社日本触媒 | アクリル酸の製造方法 |
FR2882052B1 (fr) * | 2005-02-15 | 2007-03-23 | Arkema Sa | Procede de deshydratation du glycerol en acroleine |
-
2006
- 2006-02-27 TW TW095106533A patent/TWI438187B/zh active
- 2006-02-27 TW TW101122385A patent/TWI522092B/zh active
- 2006-02-28 US US11/817,247 patent/US20090134357A1/en not_active Abandoned
- 2006-02-28 JP JP2007557408A patent/JP5554472B2/ja active Active
- 2006-02-28 BR BRPI0607884-2A patent/BRPI0607884A2/pt not_active IP Right Cessation
- 2006-02-28 EP EP06707335.3A patent/EP1866272B1/de active Active
- 2006-02-28 WO PCT/EP2006/001831 patent/WO2006092272A2/de active Application Filing
- 2006-02-28 CN CN2006800104254A patent/CN101151237B/zh active Active
-
2007
- 2007-08-27 ZA ZA200707214A patent/ZA200707214B/en unknown
-
2012
- 2012-05-07 JP JP2012105738A patent/JP2012153717A/ja active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0890591A2 (de) * | 1997-07-07 | 1999-01-13 | Idemitsu Petrochemical Co., Ltd. | Acrylatpolymer, Verfahren zu seiner Herstellung und biologisch abbaubare Builderkomponente |
US20020120085A1 (en) * | 2000-06-21 | 2002-08-29 | Nippon Shokubai Co., Ltd. | Production process for water-absorbent resin |
Non-Patent Citations (2)
Title |
---|
DATABASE WPI Section Ch, Week 200560 Derwent Publications Ltd., London, GB; Class A41, AN 2005-585659 XP002384230 & JP 2005 213225 A (NIPPON SHOKUBAI CO LTD) 11. August 2005 (2005-08-11) * |
See also references of EP1866272A2 * |
Cited By (104)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006136336A3 (de) * | 2005-06-20 | 2007-04-26 | Stockhausen Chem Fab Gmbh | Herstellung von acrolein, acrylsäure und wasserabsorbierenden polymergebilden aus glycerin |
WO2006136336A2 (de) * | 2005-06-20 | 2006-12-28 | Evonik Stockhausen Gmbh | Herstellung von acrolein, acrylsäure und wasserabsorbierenden polymergebilden aus glycerin |
WO2008007002A3 (fr) * | 2006-07-13 | 2008-02-28 | Arkema France | Catalyseur membranaire pour la synthèse d'acide acrylique à partir de glycérol |
WO2008007002A2 (fr) * | 2006-07-13 | 2008-01-17 | Arkema France | Catalyseur membranaire pour la synthèse d'acide acrylique à partir de glycérol |
FR2903620A1 (fr) * | 2006-07-13 | 2008-01-18 | Arkema France | Catalyseur membranaire pour la synthese d'acide acrylique a partir de glycerol |
US7939597B2 (en) | 2006-08-22 | 2011-05-10 | Evonik Stockhausen Gmbh | Acrylic acid and water-absorbing polymer structures based on renewable raw materials and process for their production by dehydration |
DE102006039205A1 (de) * | 2006-08-22 | 2008-03-20 | Stockhausen Gmbh | Auf nachwachsenden Rohstoffen basierende Acrylsäure und wasserabsorbierende Polymergebilde sowie Verfahren zu deren Herstellung mittels Dehydratisierung |
WO2008023040A3 (de) * | 2006-08-22 | 2008-06-12 | Stockhausen Chem Fab Gmbh | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung mittels dehydratisierung |
US8258249B2 (en) | 2006-08-22 | 2012-09-04 | Evonik Stockhausen Gmbh | Water-absorbing polymer structures based on renewable raw materials and process for their production by dehydration |
WO2008023040A2 (de) * | 2006-08-22 | 2008-02-28 | Evonik Stockhausen Gmbh | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung mittels dehydratisierung |
WO2008053646A1 (fr) * | 2006-11-02 | 2008-05-08 | Nippon Shokubai Co., Ltd. | Procédé de fabrication d'acide acrylique, appareil de fabrication d'acide acrylique et composition pour la fabrication d'acide acrylique |
WO2008061860A1 (de) | 2006-11-20 | 2008-05-29 | Evonik Degussa Gmbh | Verfahren zur herstellung von fettsäurealkylestern und acrolein aus triglyceriden |
JP2010510277A (ja) * | 2006-11-20 | 2010-04-02 | エボニック デグサ ゲーエムベーハー | トリグリセリドからの脂肪酸アルキルエステルおよびアクロレインの製造法 |
WO2008066082A1 (fr) | 2006-12-01 | 2008-06-05 | Nippon Shokubai Co., Ltd. | Procédé permettant de produire une composition contenant de l'acroléine et de la glycérine |
JP2008137950A (ja) * | 2006-12-01 | 2008-06-19 | Nippon Shokubai Co Ltd | グリセリンからのアクロレインの製法 |
US7951978B2 (en) | 2006-12-01 | 2011-05-31 | Nippon Shokubai Co., Ltd. | Process for producing acrolein and glycerin-containing composition |
JP2014156469A (ja) * | 2006-12-19 | 2014-08-28 | Arkema France | グリセロールからのアクリル酸の製造方法 |
CN101563311B (zh) * | 2006-12-19 | 2013-10-30 | 阿肯马法国公司 | 从甘油制备丙烯酸的方法 |
WO2008087315A3 (fr) * | 2006-12-19 | 2008-11-06 | Arkema France | Procede de preparation d'acide acrylique a partir de glycerol |
US8212070B2 (en) | 2006-12-19 | 2012-07-03 | Arkema France | Method for preparing acrylic acid from glycerol |
WO2008087315A2 (fr) * | 2006-12-19 | 2008-07-24 | Arkema France | Procede de preparation d'acide acrylique a partir de glycerol |
FR2909999A1 (fr) * | 2006-12-19 | 2008-06-20 | Arkema France | Procede de preparation d'acide acrylique a partir de glycerol |
JP2010513422A (ja) * | 2006-12-19 | 2010-04-30 | アルケマ フランス | グリセロールからのアクリル酸の製造方法 |
US7566804B2 (en) | 2007-01-26 | 2009-07-28 | Basf Aktiengesellschaft | Process for preparing acrylic acid |
DE102007004960A1 (de) | 2007-01-26 | 2008-07-31 | Basf Se | Verfahren zur Herstellung von Acrylsäure |
JP2010519191A (ja) * | 2007-02-16 | 2010-06-03 | アルケマ フランス | グリセロールからのアクリロニトリルの合成方法 |
EP2186790A4 (de) * | 2007-08-29 | 2013-09-04 | Showa Denko Kk | Verfahren zur herstellung von acrolein und verfahren zur herstellung von acrylsäure |
EP2186790A1 (de) * | 2007-08-29 | 2010-05-19 | Showa Denko K.K. | Verfahren zur herstellung von acrolein und verfahren zur herstellung von acrylsäure |
DE102007055086A1 (de) | 2007-11-16 | 2009-05-20 | Basf Se | Verfahren zur Herstellung von Acrylsäure |
JP2008174544A (ja) * | 2007-11-27 | 2008-07-31 | Nippon Shokubai Co Ltd | アクロレインの製造方法 |
JP5572393B2 (ja) * | 2007-12-28 | 2014-08-13 | 昭和電工株式会社 | アクリル酸の製造方法 |
US8461380B2 (en) | 2007-12-28 | 2013-06-11 | Showa Denko K.K. | Method for production of acrylic acid |
WO2009084417A1 (ja) * | 2007-12-28 | 2009-07-09 | Showa Denko K.K. | アクリル酸の製造方法 |
JP2011513487A (ja) * | 2008-03-13 | 2011-04-28 | フイナ・テクノロジー・インコーポレーテツド | トルエン及びメタンからのエチルベンゼンの製造方法 |
JP2011518111A (ja) * | 2008-04-16 | 2011-06-23 | アルケマ フランス | グリセリンからアクロレインを製造する方法 |
WO2009130915A1 (ja) * | 2008-04-25 | 2009-10-29 | 株式会社日本触媒 | ポリアクリル酸(塩)系吸水性樹脂およびその製造方法 |
JP5730013B2 (ja) * | 2008-04-25 | 2015-06-03 | 株式会社日本触媒 | ポリアクリル酸(塩)系吸水性樹脂およびその製造方法 |
DE102008001435A1 (de) | 2008-04-28 | 2009-10-29 | Basf Se | Verfahren zur Übertragung von Wärme auf eine monomere Acrylsäure, Acrylsäure-Michael-Oligomere und Acrylsäurepolymerisat gelöst enthaltende Flüssigkeit |
US8742169B2 (en) | 2008-06-05 | 2014-06-03 | Showa Denko K.K. | Acrolein manufacturing method and acrylic acid manufacturing method |
EP2145872A1 (de) | 2008-07-19 | 2010-01-20 | Cognis IP Management GmbH | Verfahren zur Dehydratisierung von Alkoholen |
JP2011528705A (ja) * | 2008-07-22 | 2011-11-24 | アルケマ フランス | 再生可能な材料からのプロピオン酸ビニルの製造と、得られたプロピオン酸ビニルと、その使用 |
US9206110B2 (en) | 2008-07-22 | 2015-12-08 | Arkema France | Method for producing bioresourced propionic acid from glycerol |
JP2012501299A (ja) * | 2008-07-22 | 2012-01-19 | アルケマ フランス | グリセロールからバイオ資源のプロピオン酸を製造する方法 |
US8440859B2 (en) | 2008-07-22 | 2013-05-14 | Arkema France | Method for producing bioresourced propionic acid from glycerol |
FR2934261A1 (fr) * | 2008-07-25 | 2010-01-29 | Arkema France | Procede de synthese d'esters de l'acide acrylique |
WO2010010309A2 (fr) * | 2008-07-25 | 2010-01-28 | Arkema France | Procede de synthese d'esters de l'acide acrylique bioressources |
WO2010010309A3 (fr) * | 2008-07-25 | 2010-03-18 | Arkema France | Procede de synthese d'esters de l'acide acrylique bioressources |
DE102008040799A1 (de) | 2008-07-28 | 2008-12-11 | Basf Se | Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enthaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal |
US8299299B2 (en) | 2008-07-28 | 2012-10-30 | Basf Se | Process for separating acrylic acid present as a main constituent and glyoxal present as a by-product in a product gas mixture of a partial heterogeneously catalyzed gas phase oxidation of a C3 precursor compound of acrylic acid |
DE102008041573A1 (de) | 2008-08-26 | 2010-03-04 | Basf Se | Verfahren zur Auftrennung von in einem Produktgasgemisch einer partiellen heterogen katalysierten Gasphasenoxidation einer C3-Vorläuferverbindung der Acrylsäure als Hauptbestandteil enhaltener Acrylsäure und als Nebenprodukt enthaltenem Glyoxal |
US8748545B2 (en) | 2008-09-16 | 2014-06-10 | Arkema France | Process for producing bio-resourced polymer-grade acrylic acid from glycerol |
FR2935971A1 (fr) * | 2008-09-16 | 2010-03-19 | Arkema France | Acide bio-acrylique de grade polymere et son procede de fabrication a partir de glycerol. |
WO2010031949A1 (fr) * | 2008-09-16 | 2010-03-25 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource de grade polymere a partir de glycerol |
FR2939055A1 (fr) * | 2008-12-03 | 2010-06-04 | Coatex Sas | Utilisation de polymeres acryliques dont l'acide acrylique est issu du glycerol, comme agent de dispersion ou de broyage de matieres minerales. |
US8524945B2 (en) | 2008-12-09 | 2013-09-03 | Evonik Degussa Gmbh | Method for producing acrolein comprising the regeneration of a raw glycerin phase |
DE102008060888A1 (de) | 2008-12-09 | 2010-06-10 | Evonik Stockhausen Gmbh | Verfahren zur Herstellung von Acrolein umfassend die Aufarbeitung einer Rohglycerin-Phase |
DE102008054587A1 (de) | 2008-12-12 | 2010-06-17 | Basf Se | Verfahren zur Rückspaltung von in einer Flüssigkeit F enthaltenen Michael-Addukten, die bei der Herstellung von Acrylsäure oder deren Ester gebildet wurde |
WO2010136697A1 (fr) | 2009-05-28 | 2010-12-02 | Arkema France | Polymere adhesif sensible a la pression contenant du methacrylate de tetrahydrofurfuryle |
WO2011000808A2 (de) | 2009-07-01 | 2011-01-06 | Basf Se | Verfahren der abtrennung von acrylsäure aus dem produktgasgemisch einer heterogen katalysierten partiellen gasphasenoxidation wenigstens einer c3-vorläuferverbindung |
DE102009027401A1 (de) | 2009-07-01 | 2010-02-18 | Basf Se | Verfahren der Abtrennung von Acrylsäure aus dem Produktgasgemisch einer heterogen katalysierten partiellen Gasphasenoxidation wenigstens einer C3-Vorläuferverbindung |
WO2011010036A1 (fr) | 2009-07-22 | 2011-01-27 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource a partir de glycerol |
WO2011010035A1 (fr) | 2009-07-22 | 2011-01-27 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource a partir de glycerol |
WO2011040575A1 (ja) | 2009-09-30 | 2011-04-07 | 株式会社日本触媒 | ポリアクリル酸(塩)系吸水性樹脂およびその製造方法 |
US10294315B2 (en) | 2009-09-30 | 2019-05-21 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt)-based water absorbent resin and method for producing same |
TWI471300B (zh) * | 2009-12-14 | 2015-02-01 | Arkema France | 由甘油製造丙烯醛及/或丙烯酸的方法 |
WO2011080447A1 (fr) | 2009-12-14 | 2011-07-07 | Arkema France | Procede de fabrication d'acroleine et/ou d'acide acrylique a partir de glycerol |
WO2011073552A1 (fr) | 2009-12-14 | 2011-06-23 | Arkema France | Procede de fabrication d'acroleine et/ou d'acide acrylique a partir de glycerol |
FR2953829A1 (fr) * | 2009-12-14 | 2011-06-17 | Arkema France | Procede de fabrication d'acroleine et/ou d'acide acrylique a partir de glycerol |
WO2011090130A1 (ja) | 2010-01-20 | 2011-07-28 | 株式会社日本触媒 | 吸水性樹脂の製造方法 |
WO2011090129A1 (ja) | 2010-01-20 | 2011-07-28 | 株式会社日本触媒 | 吸水性樹脂の製造方法 |
DE102010001228A1 (de) | 2010-01-26 | 2011-02-17 | Basf Se | Verfahren der Abtrennung von Acrylsäure aus dem Produktgasgemisch einer heterogen katalysierten partiellen Gasphasenoxidation wenigstens einer C3-Vorläuferverbindung |
FR2957594A1 (fr) * | 2010-03-18 | 2011-09-23 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource de grade polymere a partir de glycerol |
WO2011114051A1 (fr) * | 2010-03-18 | 2011-09-22 | Arkema France | Procede de fabrication d'acide acrylique bio-ressource de grade polymere a partir de glycerol |
EP2565211B1 (de) | 2010-04-26 | 2017-10-25 | Nippon Shokubai Co., Ltd. | Polyacrylsäure(salz), wasserabsorbierendes harz auf basis von polyacrylsäure(salz) und verfahren zu seiner herstellung |
US10640593B2 (en) | 2010-04-26 | 2020-05-05 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt), polyacrylic acid (salt)-based water-absorbing resin, and process for producing same |
US10640588B2 (en) | 2010-04-26 | 2020-05-05 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt), polyacrylic acid (salt)-based water-absorbing resin, and process for producing same |
US9212122B2 (en) | 2010-10-08 | 2015-12-15 | Basf Se | Process for inhibiting unwanted free-radical polymerization of acrylic acid present in a liquid phase P |
WO2012045738A1 (de) | 2010-10-08 | 2012-04-12 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
US20120100372A1 (en) * | 2010-10-23 | 2012-04-26 | Mohammad Hassan Nazaran | Chelate compounds |
DE102011076931A1 (de) | 2011-06-03 | 2012-12-06 | Basf Se | Wässrige Lösung, enthaltend Acrylsäure und deren konjugierte Base |
US9150483B2 (en) | 2011-06-03 | 2015-10-06 | Basf Se | Aqueous solution comprising acrylic acid and the conjugate base thereof |
WO2012163931A1 (de) | 2011-06-03 | 2012-12-06 | Basf Se | Wässrige lösung, enthaltend acrylsäure und deren konjugierte base |
DE102012201913A1 (de) | 2012-02-09 | 2013-08-14 | Tesa Se | Haftklebebänder auf Basis biobasierter Monomere |
EP2626397A1 (de) | 2012-02-09 | 2013-08-14 | tesa AG | Haftklebebänder auf Basis biobasierter Monomere |
EP2626397B1 (de) | 2012-02-09 | 2018-05-30 | tesa SE | Haftklebemasse umfassend Polymere hergestellt mit biobasierten Monomeren |
US9822197B2 (en) | 2012-11-26 | 2017-11-21 | Basf Se | Method for producing superabsorbers based on renewable raw materials |
WO2014079785A3 (de) * | 2012-11-26 | 2014-12-31 | Basf Se | Verfahren zur herstellung von superabsorbern auf basis nachwachsender rohstoffe |
DE102013226428A1 (de) | 2013-12-18 | 2015-06-18 | Basf Se | Extraktionskolonne und Verfahren zum Extrahieren eines Bestandteils aus einem Fluid |
US9643910B2 (en) | 2013-12-18 | 2017-05-09 | Basf Se | Extraction column and process for extracting a constituent from a fluid |
WO2015124856A1 (fr) | 2014-02-19 | 2015-08-27 | Arkema France | Procede de production d'acide acrylique bio-source |
US9776940B2 (en) | 2015-08-07 | 2017-10-03 | Basf Se | Process for production of acrylic acid |
US11447439B2 (en) | 2018-07-26 | 2022-09-20 | Basf Se | Method for inhibiting unwanted radical polymerisation of acrylic acid present in a liquid phase P |
WO2020020697A1 (de) | 2018-07-26 | 2020-01-30 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
WO2021191042A1 (de) | 2020-03-26 | 2021-09-30 | Basf Se | Verfahren zur hemmung der unerwünschten radikalischen polymerisation von in einer flüssigen phase p befindlicher acrylsäure |
WO2021224044A1 (de) | 2020-05-04 | 2021-11-11 | Basf Se | Verfahren zur rückspaltung von in einer flüssigkeit f enthaltenen michael-addukten, die bei der herstellung von acrylsäure gebildet wurden |
WO2022018013A1 (en) | 2020-07-20 | 2022-01-27 | Basf Se | Aqueous polymer latex of film-forming copolymers suitable as binder in waterborne coating compositions |
WO2022034247A1 (de) | 2020-08-14 | 2022-02-17 | Tesa Se | Haftklebmasse |
WO2023006503A1 (de) | 2021-07-28 | 2023-02-02 | Basf Se | Verfahren zur herstellung von acrylsäure |
WO2023148332A1 (en) | 2022-02-04 | 2023-08-10 | Basf Se | Polymer binder based on 2-octyl acrylate, n-butyl acrylate and methyl methacrylate for aqueous coating compositions containing titanium dioxide |
DE202022101833U1 (de) | 2022-04-06 | 2022-04-25 | Basf Se | Öl-basierte Bohrflüssigkeiten mit Copolymeren aus Styrol, 2-Octylacrylat und (Meth)acrylsäure |
DE202022101834U1 (de) | 2022-04-06 | 2022-04-25 | Basf Se | Polymethylmethacrylat (PMMA) mit 2-Octylacrylat-Comonomer |
DE202022101962U1 (de) | 2022-04-12 | 2022-04-29 | Basf Se | Alkyl(meth)acrylat-Polymere enthaltend 2-Octylacrylat zur Hydrophobierung von Textilien |
DE202022102002U1 (de) | 2022-04-13 | 2022-04-25 | Basf Se | Härtbare Zusammensetzungen enthaltend 2-Octylacrylat zur Boden- und Fahrbahnbeschichtung |
DE202023100921U1 (de) | 2023-02-27 | 2023-04-11 | Basf Se | Härtbare Zusammensetzung enthaltend 2-Octyl(meth)acrylat |
Also Published As
Publication number | Publication date |
---|---|
TWI522092B (zh) | 2016-02-21 |
JP5554472B2 (ja) | 2014-07-23 |
US20090134357A1 (en) | 2009-05-28 |
CN101151237A (zh) | 2008-03-26 |
JP2008531628A (ja) | 2008-08-14 |
CN101151237B (zh) | 2011-10-26 |
TW200643009A (en) | 2006-12-16 |
EP1866272B1 (de) | 2017-10-18 |
TW201242580A (en) | 2012-11-01 |
BRPI0607884A2 (pt) | 2009-10-20 |
JP2012153717A (ja) | 2012-08-16 |
EP1866272A2 (de) | 2007-12-19 |
ZA200707214B (en) | 2008-07-30 |
WO2006092272A3 (de) | 2007-04-26 |
TWI438187B (zh) | 2014-05-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1866272B1 (de) | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung | |
EP2061742B1 (de) | Auf nachwachsenden rohstoffen basierende acrylsäure und wasserabsorbierende polymergebilde sowie verfahren zu deren herstellung mittels dehydratisierung | |
EP1863917B1 (de) | Verfahren zur herstellung eines wasserabsorbierenden polymergebildes basierend auf acrylsäure | |
WO2006136336A2 (de) | Herstellung von acrolein, acrylsäure und wasserabsorbierenden polymergebilden aus glycerin | |
EP2066611B1 (de) | Verfahren zur herstellung von durch kristallisation gereinigter acrylsäure aus hydroxypropionsäure sowie vorrichtungen dazu | |
EP1417164B1 (de) | Verfahren zur herstellung wasserabsorbierender harze | |
EP1926700B1 (de) | Verfahren zur herstellung von (meth)acrylsäure mit schwersiedeaufarbeitung durch kristallisation | |
DE102008044946B4 (de) | Einsatz von Schaumkörpern in Oxidations-Reaktoren zur Herstellung ungesättigter Carbonsäuren | |
EP1940766B2 (de) | Neutralisationsverfahren | |
WO2005005514A1 (de) | (meth)acrylsäureester monoalkoxilierter polyole und deren herstellung | |
EP1689796A1 (de) | (meth)acrylsäureester ungesättigter aminoalkohole und deren herstellung | |
DE102012200996A1 (de) | Verfahren zur Herstellung von Ethylen und anderen Olefinen aus wässrigen Lösungen der korrespondierenden Alkohole | |
EP1682480B1 (de) | Verfahren zur herstellung von benzoesäureestern | |
WO2015036218A1 (de) | Verfahren zur dehydratisierung von 3-hydroxypropionsäure zu acrylsäure | |
DE102008038273A1 (de) | Ein Verfahren zur Herstellung von Acrylsäure und daraus herstellbaren Verbindungen basierend auf Glycerin mit Wechselkatalysator | |
EP3145965B1 (de) | Verfahren zur kontinuierlichen dehydratisierung von 3-hydroxypropionsäure zu acrylsäure | |
EP1318136B1 (de) | Verfahren zur Herstellung von gesättigten Carbonsäuren mit ein bis vier C-Atomen durch Gasphasenoxidation von 2-butanon | |
EP3619243B1 (de) | Verfahren zur diskontinuierlichen herstellung von superabsorberpartikeln durch polymerisation einer in einem hydrophoben lösungsmittel dispergierten wässrigen monomerlösung | |
DE10138101A1 (de) | Verfahren zur Abtrennung von Acrylsäure aus den Reaktionsgasen der katalytischen Gasphasenoxidation | |
WO2024083322A1 (de) | Verbessertes verfahren zur depolymerisierung von polyethylenterephthalat |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DPE2 | Request for preliminary examination filed before expiration of 19th month from priority date (pct application filed from 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2007557408 Country of ref document: JP Ref document number: 2007/07214 Country of ref document: ZA Ref document number: 6628/DELNP/2007 Country of ref document: IN |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REEP | Request for entry into the european phase |
Ref document number: 2006707335 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006707335 Country of ref document: EP Ref document number: 200680010425.4 Country of ref document: CN |
|
WWP | Wipo information: published in national office |
Ref document number: 2006707335 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 11817247 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: PI0607884 Country of ref document: BR Kind code of ref document: A2 |