• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 优先权
    • 专利摘要:
    Summary Procedure for treatment ay talloljebeck. According to this process, some of the fatty acids and resin acids are liberated from their sterol and trasprite esters and converted to methanol esters or ethanol esters. The transesterified products are removed from the stream by evaporation and then condensed, and by hydrogenation of the obtained condensate the acids are decarboxylated and the double bonds are matted. It is possible that any of the present invention for producing motor fuel from tall oil pitch.
    公开号:SE537513C2
    申请号:SE1200658
    申请日:2011-03-28
    公开日:2015-05-26
    发明作者:Juhani Saviainen；Mikko Rintola；Timo Saarenko
    申请人:Forchem Oy；
    IPC主号:
    专利说明:

    The present invention relates to a process for the treatment of tall oil pitch in accordance with the preamble of claim 1.
    In such a process, the composition treated from tall oil contains the sterol esters of resin-derived fatty and resin acids and optionally esters of other trasprites.
    The present invention further relates to a product according to claim 15.
    Tall oil is one that is obtained as a by-product in the cellulose industry. It is already possible that tall oil contains resin acids, fatty acids, sterols and other rubbing alcohol as well as small amounts of inorganic compounds, such as Na2SO4, which are residues from cellulose cooking. Tall oil also contains metal cations, which are derived from wood and goods; from the following basic names: Ca, Fe, Mg, P, Al, Zn, Mn, V, As and Si. Tall oil may also contain other inorganic compounds. These most commonly occur in the form of resinate and / or salts of fatty acids. Their levels are usually 140-280 ppm. This means that they bind materials about 6.7 - 7.5 times their own molecular weight. Depending on the concentration, the materials in question bind e.g. resin acids 900 - 1900 ppm = maximum 0.2% by weight in crude oil and about 0.6% in pitch from tall oil distribution.
    Tall oil pitch, which is a residue from distillation distillation, was usually burned mixed with the distillate of the tall oil distillation. Tall oil pitch contains about 13% free resin acids, about 3 - 8% free fatty acids, only about 1% free sterols and about 12% bound sterols and about 60% fatty acid esters and fatty acid esters of trasprit. In addition, pitch contains a small amount of lignin, the molecular weight of which is usually over 1000, and dimers and oligomers of resin acids. the intention is that any pitch to produce motor fuel from the fatty and resin acids that the pitch contains, the metal residues must be removed. The fuel containing metal residues is not suitable for engine operation; in addition, these residues become catalyst poisons during the hydrogenation process, which is carried out in the production of motor fuels to stabilize the fuel and to prevent it from oxidizing and to lower the solidification point. According to a solution described in published patent application No. WO 2009131510, the removal of these cations is carried out with a sulfuric acid and phosphoric acid treatment and a subsequent filtration through a <10 lam filter. According to the patent application, crude tall oil (CTO) is used in the treatment.
    However, a treatment according to the edge procedure does not completely remove zinc, vanadium and arsenic. If the deposits are realized by carrying out each acid treatment separately, the precipitation being almost complete, the process becomes expensive and complicated. Consequently, when CTOs are treated according to the degree of solution, a large amount of material must be treated. This treatment does not remove lignin, but instead makes it tower. annu looser.
    U.S. Patent No. 4,426,322 discloses a CTO treatment by means of water under pressure, with which water the water-soluble salts, mainly Na 2 SO 4, are deposited, preferably at a temperature of 130 ° C, from the tall oil before the distillation treatments. However, this treatment does not remove the cations bound to the resin acids and fatty acids, nor the suspended fibers.
    According to U.S. Patent No. 4,248,769, sulfate monkey is washed with a solution of concentrated Na 2 SO 4 prior to acidification, whereby it is possible to deposit about 50% of the lignin salts, i.e. lignan20 erna.
    U.S. Patent Application Laid-Open No. 2009/0217573 A1 describes how fuel combustion engine fuel is produced from ratall oil. According to this, the ratall oil is esterified with alcohol (C1-C8), the water and the alcohol are separated, the remaining dry ester mixture is distilled into two fractions and the amount of sulfur compounds is reduced by removing them by distillation in different steps.
    An article in the journal Energy & Fuels (2001. 15, 1166-1172) describes how a resin acid fraction of edible oil is converted into motor fuel. According to this article, the first - COOH - groups are removed by converting them to alcohols or hydrocarbons by thermal fission, whereby CO2 is removed. This requires a temperature of about 400 ° C and a Ni-Mo catalyst. According to the same article, it is possible to directly hydrate the resin acids at a temperature of 350-400 ° C and at a water pressure of 100 bar while using a Ni-Mo oxide catalyst on the surface of alumina. In this way it is possible to produce 2 cycloalkanes and hydrogenated "aromatics".
    The tests in this publication were so interesting that a pure resin fraction was used in them (Unitol NCY / Arizona Chemicals). The boiling point of the majority of the product obtained was about 320 ° C at normal pressure.
    U.S. Patent No. 5,705,722 discloses that tall oil, which is substantially free of ash (a distilled product, the bottom product of which is tall oil pitch), is hydrogenated at a 4MPa H 2 pressure and at a temperature of 370-450 ° C. The cetane index of a product produced in this way is pasted to be so good that it can be used as an additive in petrochemical diesel of poor quality.
    The patents described above systematically utilize fractions from which high molecular weight chemicals have been derived, or according to some publications, laboratory tests have been performed with "pure" chemicals. Tall oil, and in particular its pitch, contains large amounts of cations, which are catalyst poisons. Consequently, procedures based on the hydrogenation of pure chemicals are not industrially applicable.
    The object of the present invention is to eliminate at least some problems in relation to prior art and to provide a completely new method for treating tall oil pitch, in particular to treat it in such a way that it is possible to obtain motor fuel or an additive for this industry.
    This invention is based on the idea of first releasing the resin and fatty acids which pitch contains from its esters. This can be achieved by e.g. use water hydrolysis or transesterification or a combination thereof, the transesterification being carried out in particular by means of a low molecular weight alcohol. The fatty acids or their lower alkyl esters, which have been liberated from a high molecular weight ester, are then removed from the pitch by distillation or, preferably, evaporation. The anta is condensed and recovered.
    It has been found that the evaporation is preferably carried out by means of a device, the pitch is usually treated with so much salt that it does not substantially boil on the evaporation surface. A preferred embodiment refers to a shortwave evaporator, i.e. a device, accustomed to the surface to be heated and the cooling surface lying opposite each other and accustomed to the gas flow separated from the evaporated liquid, is very slow due to large heating and condensing surfaces. By using such a device, the number of droplets and other particles carried by the gas flow is minimal.
    It is possible to hydrogenate the products prepared in the above-mentioned manner, whereby the double bonds of the fatty acids of the fatty acids are hydrogenated, i.e. matte, and the fatty acids -COOH or -COOCH3 - are converted to carbon dioxide and methane or ethane. The alkyl esters of the resin acids are subjected to a similar phenomenon with the difference that their ring structure is at least partially opened. When this salt is used, a bio-component is obtained, which is suitable for use as a motor fuel, e.g. diesel fuel.
    More specifically, the method according to the invention can be characterized mainly by what is stated in the preamble of claim 1.
    The product according to the present invention is characterized by what is stated in claim 15.
    Significant advantages are achieved with the present invention. Salunda it is possible to intend Tart increase the economic value of the components of tall oil pitch in comparison with only burning it.
    Since most of the esters of fatty acids and resin acids, and the free fatty acids and resin acids have been released by evaporating from the pitch, sterols which have also been released remain in the pitch and which are t.o.m. more valuable than the fatty acids.
    Of the metals present in tall oil, Zn, As, Fe, Si and Pb, and according to some experts alien Na and Ca, are harmful catalyst poisons, as they tap into the pores of the actual catalyst bar, such as activated carbon and Al 2 O 3. The first four metals in the uplift, i.e. Zn, As, Fe, Si and Pb, also emit hydrogenation catalyst poisons. In addition, metals, together with e.g. Phosphorus, which is present in the automotive industry, is the catalyst toxins of exhaust gas converters, among which lead is the most harmful. In the jet engine industry, the maximum permissible amount of metals together amounts to 5 - 98 ppb (0.001 ppm), depending on written sources.
    Copper, in turn, is the most harmful metallic dirt in the finished industry. Even at levels of 25 Ile, it causes oligomerization of molecules (rubber resin). Consequently, the metals must be carefully removed from fatty acids and resin acids obtained from tall oil pitch, and in general from the industry produced from tall oil products.
    WO / 2010/003504 describes a process for adsorbing and absorbing metals from diesel fuel. This solution relates to the removal of Cu, Pb and Zn cations by using fatty acids (R2COOH) impregnated on a bar powder.
    The pure and metal-free fatty acids and resin acids or their alcohol esters, which can be obtained by means of the present invention, are de facto highly unsuitable as they are used as a fuel in diesel engines. It is possible to hydrate the fatty acids, also together with the resin acids, in order to obtain t.o.m. gas turbine fuel.
    In the following, the present invention is further investigated with the aid of a detailed description.
    The accompanying drawing shows a flow chart according to a preferred embodiment of the present invention.
    In general, the present invention relates to the following: a substantial portion of the fatty acids and resin acids are liberated from their sterol esters and possibly from their other substituent esters, Preferably they are converted to methanol or ethanol esters or similar lower alkyl esters, the transesterified products are removed preferably immediately, and if desired, the resulting condensate is hydrogenated.
    By "a substantial portion" is meant that at least about 50 mole percent, most preferably at least 70 mole percent, especially at least 80 mole percent of the sterol alcohols and trasprites of the fatty acids and resin acids that the pitch possesses are released from their esters and converted to layers. alkyl esters.
    By a "lower alcohol" is meant having C 1-4 alcohol, preferably methanol or ethanol.
    According to the present invention, there are at least two approaches (see figure), depending on how the fatty acids and resin acids are released from the sterol esters and possibly from other alcohol esters. It is also possible to combine these two. salt.
    In the first embodiment named "Option 1" in the figure, the process starts with a water hydrolysis, which preferably consists of an acid hydrolysis. In the figure, reference number 1 refers to the hydrolysis step. Loose salts, and at least some of the cations bound to the resin acids, are dissolved in water, which is precipitated by decantation after hydrolysis. In the figure, reference number (2) refers to the drying step.
    Preferably, the hydrolysis is carried out at a temperature of about 250-360 ° C and correspondingly at a pressure of 40-86 bar, and further the clamping is carried out at a temperature of about 95 ° C. It is also possible to operate at a temperature of about 220-280 ° C and correspondingly at a pressure of 25-65 bar.
    Now the soluble salts and at least some of the salts dissolved due to acidity are still in their aqueous phase.
    The water hydrolysis described above may be partial or only an aqueous water. It is important that in as many steps as possible, as much metals, phosphorus and solids as possible are removed from the fatty acids, resin acids and / or their lower alkyl esters (methyl or ethyl esters) released from the pitch. After any water treatment, the fatty acid mixture to be esterified must be carefully dried. If the mixture has not been subjected to estrification at all, but is distilled off and hydrated after liberation either at the original distillation site or elsewhere, then the liberation from the metals is equally important.
    A special feature of the water hydrolysis is that the dissolved salts are deposited together with the excess water, assuming that at least a large part of the water is decanted before the water evaporation to release it from organic material. By water or water anhydrolysis is meant a pretreatment before a possible alcohol esterification.
    Instead of water hydrolysis 1, it is possible to carry out only one water wash, drying and 6 transesterification. In this way, it is possible to deposit most of the salts (Na2SO4).
    Methanol or ethanol can also be used in a water hydrolysis to help dissolve the emulsions and by contributing to the transesterification (J. Am. Chem. Soc., 2001, 123 (41) pp. 10101-10102).
    The transesterification 3 is then carried out with a lower alcohol, typically a C1-4 alcohol, such as methanol or ethanol, after the reaction mixture has been dried.
    According to another embodiment, direct transesterification is used which is carried out with the above-mentioned lower alcohol, such as methanol or ethanol (this solution is called alternative "Option 2"). Also in this case, an acid catalyst is used which facilitates the separation of the metals into the generated aqueous phase, which has been removed by decantation or centrifugation or evaporation.
    The pressure and temperature of the transesterification are chosen depending on how much alcohol is raised in the pitch and which of the mixture's pressure. In general, the pressure is chosen so that it does not matter that the alcohol cannot boil off at the selected temperature. In Salunda, the temperature is generally in the range 25-300 ° C, e.g. about 50-250 ° C, and the pressure is normal air pressure or higher, e.g. maximum 150 bar (abs), most suitable maximum 100 bar (abs), e.g. about 2-90 bar (abs).
    The transesterification is most conveniently carried out with methanol or ethanol using an acid catalyst, e.g. sulfuric acid or an acidic ion exchange resin.
    These transesterifications and subsequent drying and evaporation are always carried out one after the other.
    To make maximum use of the pitch, e.g. in the production of motor fuel, the fatty acids to be released from the esters are separated by distillation 6.
    There are many separation procedures. It is possible to perform the separation e.g. with either a fractionation column, which generally comprises flake kind of return, 7 or only by "stripping distillation", the column not comprising a return, but comprising a plurality of separation bottoms, or a thin film evaporator or "shortwave evaporator".
    When fatty acids or their esters are evaporated, it is important that they are evaporated without boiling.
    Therefore, it is possible to use a thin film evaporator, but preferably the evaporator used is a "shortwave evaporator", which comprises a separate drip separator.
    In a shortwave evaporator, the condensing surface and the evaporation surface are in the same space and are approximately the same size. The gases move a short distance at low speed. This salt ensures that the metal cations do not migrate from the heating surface to the condensing surface. When pure fatty acid esters are obtained in this way, it is possible to carry out a possible hydrogenation treatment of them because the catalysts are not poisoned with metals.
    It is advantageous to use a short-wave evaporator because then the smallest possible amount of metals, if any, is transferred to the distillate or evaporator. This is important so that when the alkyl esters (typically methyl esters) of liberated fatty acids and resin acids are used for the production of diesel fuel by means of hydrogenation, the hydrogenation catalysts are not contaminated. It is advisable to feed these esters, together with petrochemical raw material, directly for further processing at an oil refinery.
    In both cases, both the water and the excess alcohol from the transesterification ring must first be removed by evaporation in a separate unit 4 and not before that the methyl esters of the fatty acids and resin acids are separated in a high vacuum from the other constituents of the basin.
    According to a preferred embodiment of the present invention, the sterol compounds are evaporated at a substantially lower pressure, after the esters of the fatty acids and the resin acids have been deposited by evaporation. Another possible treatment is that after the evaporation of the liberated acids, the remaining distillation residue of the pitch is dissolved into a lower alcohol, in particular into C1 or C2 alcohol, and the separated alcohol phase is evaporated and the sterols are used for further purification. In both cases, the sterols are distilled or evaporated at a lower pressure than the fatty acids (T 8 is in particular about 225 ° C, p = 0.01-3.5 mbar).
    The evaporated alkyl ester obtained is most preferably condensed immediately after evaporation. The condensation is typically carried out within about 1-60 minutes, especially within about 1-10 5 minutes after evaporation.
    According to another preferred embodiment, the treatment consists in that a product, accustomed to the fatty acids and the resin acids, is no longer bound to form high molecular weight esters, dried to release them from water (after decanting) and then evaporated, preferably in two steps. .
    In this case, a composition of fatty acid methyl ester and resin acid methyl ester is obtained in the condensate of the derivative in the first step 5, and a sterol composition in the following step 6. The residue comprises neutral materials and oligomers with a high boiling point. The residue contains dven metal resinate.
    In the first step, the operating pressure amounts to about 3 - 15 mbar (abs.) And the operating temperature to 220 ° C, and in the second step - as described above - the operating temperature most easily states to about 225 ° C and the operating pressure to 0.01 - 3, 5 mbar (abs).
    On this sieve, it is possible to utilize about 60 - 70% of the basin constituents, free from metal salts.
    Although it is possible to successfully use methyl esters as such as a fuel for diesel engines (Biorcsource Technology volume 98, published 2 Jan 2007 pp. 241-246), the product is susceptible to oxidation and oligomerization.
    Accordingly, the alkyl ester fraction of the fatty acid and the resin acid is catalytically hydrogenated and isomerized if necessary to increase the cetane index. By means of hydrogenation, it is possible to decarboxy30 clay the acids and meet the double bonds.
    If in this step it is desired to use the sterol fraction for final purification, it is separated by evaporation at a lower pressure. The hydrogenation can be carried out on one salt 'cant per se, e.g. as described in the publication Petroleum and Science and Technology 16 (5 & 6), 597-609 9 (1998).
    The pitch remaining after evaporation ("residual pitch" in the figure), which contains dimeric resin acids, oligomers, lycopene and spirits, i.e. lutein and neoxanthine, etc., and metal salts of resin acid, either burned or used as raw materials for adhesives.
    An article in the journal Petroleum and Science and Technology [16 (5 & 6), 597-609 (1998)] describes how tall oil, from which the pitch is depotched (Depitched Tall Oil = DPTO), excellently improves by hydrogenation the cetane index of diesel oil. The article studied in particular the poisoning of catalysts. It is obvious that the poisoning of catalysts is significantly more likely to be due to the use of pitch than to the use of DPTO, which poisoning is caused by relatively much higher metal contents.
    In the manner described above, a composition is obtained, the metal contents of which together amount to less than 50 mg / liter and furthermore the (Cu + Pb + Zn) contents together amount to a maximum of 300 ug / liter.
    Finally, some remarks on how the present invention is applied to a tall oil refinery.
    In principle, it is possible to use a tall oil refinery to carry out the reactions and physical separations described above. Savida short-wave evaporators are not available, am / ands a thin-film evaporator-drip separator and distillation column, used in already a laid back-flow ratio separates stinky metal resins. However, the advantages of using a short-circuit evaporator are a small pressure drop and the lower temperature of the evaporation surface.
    A normal tall oil distillery with a capacity of e.g. 150,000 tons / a fatty acids and resin acids, produces about 60,000 tons / a tall oil pitch. Since only pitch is now treated in the above-mentioned distillery and the bottom boilers used consist of either thin-film evaporators or fall-film evaporators, and they operate in a substantially lower capacity, the surface boiling is so insignificant that hardly any unwanted metal compounds move to the distillate.
    The transfer of material from the heating surface to the condensing surface is almost exclusively limited to the evaporation of molecules, when a short-wave evaporator or one of the majority of ordinary evaporators is used, such as a thin film evaporator and a falling film evaporator, at a capacity much longer than the heat.
    According to the first preferred alternative, the evaporation is carried out in a falling film evaporator, at a capacity which is 1/3 - 1/2 of the evaporator's originally planned capacity.
    According to another preferred alternative, the evaporation is performed in a thin film evaporator, at a capacity that is 1/3 - 1/2 of the evaporator's originally planned capacity. 11
    权利要求:
    Claims (6)
    [1]
    Process for the production of fuel, in particular for the production of fuel for motor vehicles, such as diesel fuel by treatment of tall oil pitch containing from tall oil resin esters of fatty alcohols and resin acids and optionally esters of other traal alcohols, characterized in that the fatty acids and at least some are released from their sterol and traalkoal alcohol esters and converted to lower alkyl esters, and the alkyl esters thus obtained are aylagged by evaporation from the pitch and subsequently condensed.
    [2]
    Process according to Claim 1, characterized in that the fatty acids and the resin acids are first released at least in part from their above-mentioned sterol or traalkohalo esters, which typically have a high molecular weight, by using water hydrolysis.
    [3]
    Process according to Claim 1 and / or 2, characterized in that the fatty acids and the resin acids are liberated from their above-mentioned sterol or traalkoal alcohol esters, which typically have a high molecular weight, by subjecting them to a transesterification reaction together with lower alcohols.
    [4]
    A method according to claim 1, characterized in that the pitch is treated on such a salt that it substantially does not boil on the evaporation surface.
    [5]
    A method according to any one of claims 1 to 4, characterized in that the treatment is carried out in a shortwave evaporator.
    [6]
    A method according to any one of claims 1 to 4, characterized in that the treatment is carried out in a case film evaporator yid
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    引用文献:
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FI20105308A|FI126337B|2010-03-26|2010-03-26|Procedure for utilizing tall oil pitch|
    PCT/FI2011/050256|WO2011117474A1|2010-03-26|2011-03-28|Method of utilizing tall oil pitch|
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