• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a process for preparing a polyol having three or four hydroxyl groups by subjecting the aldolization product from aldehyde and formaldehyde in the presence of water to hydrogenation in the presence of a hydrogenation catalyst at a high temperature. The aldehyde is obtained by aldolization of an aldehyde having at least two? -Hydrogen atoms and a formula R 1 CHO and formaldehyde in the presence of 20-70 wt%, preferably 40-60 wt%, of an anion exchange resin . The hydrogenation reaction is preferably carried out in the presence of water. In the above formula R 1 CHO, R 1 is hydrogen, an alkyl group having 1-7 carbon atoms which may have a cycloalkyl substituent, a cycloalkyl group, an aryl group, and an aralkyl group having 1-7 carbon atoms in the alkyl chain Select from.
    公开号:KR20020040682A
    申请号:KR1020017016635
    申请日:2000-06-30
    公开日:2002-05-30
    发明作者:살미타피오；세르라-홀름발렌티나；란타킬라티이나-카이사；마아키-아르벨라파이비；린드포르스라르스-페테르；노우시아이넨한누
    申请人:다이니아 케미컬스 오이；
    IPC主号:
    专利说明:

    PROCESS FOR THE PREPARATION OF POLYOLS < RTI ID = 0.0 >
    [2] Polyols and especially 1,1,1-trimethylol propane (TMP) are important as starting materials and intermediates in the production of synthetic resins such as polyester resins.
    [3] These compounds are also used for the production of plasticizers, synthetic lubricants, surfactants and the like.
    [4] A polyol such as 1,1,1-trimethylol propane can be obtained by reacting formaldehyde and another aldehyde, for example, in the presence of a strong alkaline catalyst such as sodium hydroxide, potassium hydroxide or calcium hydroxide, Of an alcohol.
    [5] However, large amounts of formate salts are produced as byproducts and this method is not economically effective in commercial terms.
    [6] In another modification, aldolization of formaldehyde and another aldehyde is carried out in the presence of an amine catalyst such as triethylamine, followed by hydrogenation.
    [7] The aldolization reaction may be carried out using an anion exchange resin acting as a catalyst.
    [8] In the specification of DE 195 420 36, a method for producing polyalcohol is described, wherein an alkanal or ketone is reacted with formaldehyde in an aqueous solution in the presence of an amine and then reacted with formaldehyde to form a cannirole methanol, excess amine, and excess formaldehyde were separated from the cannizzarro-reaction.
    [9] The remaining reaction mixture was heated to produce a polyalcohol formate.
    [10] The resulting polyalcohol formamate was subjected to a trans-esterification reaction with an alcohol in order to obtain a predetermined polyalcohol and separated in the reaction mixture.
    [11] In this specification, isobutyraldehyde is reacted with a tertiary amine, preferably triethylamine, and the periodic table IB, IVA, IVB, VA, Reacted with paraformaldehyde in the presence of at least one oxide of the elements of groups VB, VIB and VII, and then the resulting monomer and dimer hydroxypivaldehyde are hydrogenated.
    [12] In the specification of USP 5,146,012, a reaction product comprising hydroxypivaldehyde is obtained by reacting isobutyraldehyde with paraformaldehyde, a mixture of a reaction product having an alcohol, preferably about 40-90% methanol, is produced, Discloses a method for producing neopentyl glycol by contacting a mixed liquid with hydrogen in the presence of a hydrogenation catalyst.
    [13] In the process for preparing polyols described in the patent document FI 965268, formaldehyde and other aldehydes having at least two carbon atoms are subjected to aldolization reaction in the presence of a weakly basic anion exchange resin, Hydrogenation was carried out in the presence of a catalyst.
    [14] In the specification of the patent document FI 974638, it is described in the specification of FI 974638 that in the liquid phase composed of 1 to 70 wt% of a solvent, preferably an aliphatic alcohol or an ether or a mixture thereof, and 15 wt% or less of water in the presence of a nickel- Is hydrogenated to prepare neopentyl glycol.
    [15] The specification of JP 10227608 discloses a method for purifying dimethylol alkanals.
    [16] The unreacted formaldehyde was separated from the dimethylol alkanal-containing reaction product, and the reaction product was a hydroxide, carbonate or bicarbonate of an alkali metal or an alkaline earth metal, or other basic catalyst such as an anion exchange resin And condensation reaction of aliphatic aldehyde and formaldehyde in the presence of water.
    [17] Water is added to the reaction product so that the content of water is about 4 times by weight based on the formaldehyde content in the reaction product solution, and the obtained mixed solution is supplied to a thin film vaporizer, And the resulting formaldehyde vapor and steam were distilled at one end of the thin film vaporizer to purify the dimethylol alkanal.
    [18] As described above, it can be seen that there are several technical problems in the method according to the prior art.
    [19] As an example, an undesirable side reaction occurred in the first treatment step of the process for producing 1,1,1-trimethylol propane (TMP) and in the aldolization reaction treatment step of the aldehyde.
    [20] When 2-ethyl-3-hydroxypropanol is produced by reacting a starting material such as n-butanal with formaldehyde, 2-ethylpropanol (ethyl acrolein) is obtained by dehydration.
    [21] 2-ethyl-3-hydroxypropanol also reacted with formaldehyde to produce the desired intermediate 2-ethyl-3-hydroxy-2- (hydroxymethyl) propanol (TMPA).
    [22] Due to the adverse reaction, the yield of aldol and the yield and purity of the final product decreased in the aldolization reaction step.
    [23] The aldol product 2-ethyl-3-hydroxy-2- (hydroxymethyl) propanal contains an unreacted amount of unreacted formaldehyde.
    [24] This unreacted formaldehyde affects the step of hydrogenation by the catalyst as a catalyst inhibitor.
    [25] It is necessary to use a large amount of a hydrogenation catalyst in order to prevent and compensate for the inhibitory effect of formaldehyde in the hydrogenation reaction, and as a result, there is a disadvantage of increasing the size and cost of the reactor.
    [26] Typically, the number of phases of one component depends on its temperature and concentration.
    [27] If the concentration of formaldehyde increases at low temperatures, especially below 50 ° C, solid paraformaldehyde is formed, which can lead to severe blocking problems.
    [28] In view of the above-mentioned conventional drawbacks, it is necessary to improve the production method of the polyol to improve the yield, purity, conversion and selectivity.
    [1] The present invention relates to a process for the production of polyols having three or four hydroxyl groups by hydrogenating an aldolisation product from aldehydes and formaldehyde in the presence of water in the presence of a hydrogenation catalyst at a high temperature.
    [29] The present invention relates to a process for the production of polyols by aldolization of aldehydes and formaldehyde over an anion exchange resin catalyst and hydrogenation of the aldol product on a supported metal catalyst.
    [30] The technical features of the process for preparing the polyol are set forth in the claims.
    [31] It will be understood by those skilled in the art that the above-described objects can be achieved and overcome the drawbacks of the prior art methods.
    [32] The polyol can be usually prepared by subjecting an aldolization reaction to hydrogenation of the aldol product.
    [33] The aldolization reaction is preferably carried out in the presence of water, in the presence of an anion exchange resin and indeed in an alcohol-free environment, and the subsequent hydrogenation reaction of the aldol product is preferably carried out in the presence of water.
    [34] In the process for producing a polyol having 3 or 4 hydroxyl groups according to the present invention, the aldehyde is preferably an aldehyde having 20 to 70 wt% of aldehyde and formaldehyde having at least two -Hydrogen atoms represented by R 1 CH 2 CHO, Is obtained by subjecting an aldolization reaction in the presence of 40-60 wt% of water, and hydrogenating the obtained aldehyde.
    [35] In gastroesophageal R 1 CH 2 CHO, R 1 is hydrogen, aralkyl having from cycloalkyl groups having from 1 to 7 carbon atoms which can have any substituent, a cycloalkyl group, an aryl group and 1-7 carbon atoms carbon atoms in the alkyl chain kilgi Select from group.
    [36] In practice, in an alcohol-free environment, the aldolization reaction can be carried out in the presence of 0-20 wt%, preferably 0-12 wt% methanol.
    [37] In the aldolization reaction, an aldehyde having at least two -Hydrogen atoms and formaldehyde are reacted in the presence of an anion exchange resin at a molar ratio of formaldehyde to aldehyde of 2: 1 to 6: 1, 50-70 < 0 > C.
    [38] A suitable anion exchange resin catalyst, preferably a weakly basic anion exchange resin, can be treated and the upper limit of the reaction temperature is limited by the heat resistance of the anion exchange resin used.
    [39] The anion exchange resin may be a primary amine (-NH 2 ), a secondary amine (-NHR where R is an alkyl or aryl group), a tertiary amine (-NR 2 where R is as above and R is the same or different Alkyl group) and mixtures thereof.
    [40] The resin matrix used is preferably a condensation product of epichlorohydrin and an amine or styrene copolymer such as ammonia, phenol resin, acrylic resin or chloromethylated styrene-divinylbenzene copolymer.
    [41] Suitable weakly basic anion exchange resins are described in the specification FI 965268.
    [42] The aldolization reaction is preferably carried out under inert gas pressure, such as nitrogen, and can be carried out as a batch process, a semibatch process, preferably a continuous process.
    [43] The effect of methanol on the TMP-aldol yield (Y) is shown in the following graph.
    [44] 1. Three different experiments were conducted (methanol 0wt%, 6wt%, 18wt%) and in the experiment without methanol, paraformaldehyde was used.
    [45] Graph 1
    [46] The TMP-aldol yield in the presence of methanol
    [47] Code Description
    [48] ◆: TMP-aldol yield (Y) in the presence of 18 wt%
    [49] (TMP-Aldol yield (Y) in the presence of 6 wt%
    [50] (Y): TMP-aldol yield (Y) in the presence of 0 wt%
    [51] The molar ratio of formaldehyde to aldehyde was 4: 1
    [52] Temperature 70 ° C
    [53] Water 55wt%
    [54]
    [55] The effect of the water content on TMP-aldol yield (Y) in an environment without methanol is shown in the following graph 2.
    [56] The molar ratio of formaldehyde to aldehyde is 4: 1 and the TMP-aldol yield (Y) for three different water concentration values after 5 hours at 70 ° C is found to be maximum at the water content of 55 wt% in the reaction mixture .
    [57] Graph 2
    [58] Effect of Water Content on TMP-Aldol Yield (Y) in Methanol-Free Environments
    [59]
    [60] Following the aldol reaction treatment step, the aldol product was hydrogenated.
    [61] The hydrogenation reaction is carried out at a temperature of 50 to 200 DEG C, preferably 60 to 90 DEG C under a pressure of 1 to 200 bar, preferably 10 to 80 bar.
    [62] Solvents can be used selectively in the hydrogenation reaction. Suitable solvents include aliphatic alcohols such as methanol, ethanol and propanol, and have a content of 0 to 70 wt%, preferably 30 to 50 wt%.
    [63] However, in the case where formaldehyde is contained in the aldolization mixture after the aldolization reaction treatment step, it is effective to use only water as a solvent in place of alcohol in the hydrogenation of the aldol product using the Ni catalyst as the hydrogenation catalyst .
    [64] Typically, formaldehyde delays the hydrogenation of the aldol product, but the hydrogenation of the aldol product is significantly increased when only water is used as the solvent.
    [65] A suitable water concentration is 0-90 wt%, preferably 20-90 wt%.
    [66] The aldol product can be selectively purified before the hydrogenation reaction by steam distillation in which the obtained aldolization reaction mixture and water are mixed and distilled.
    [67] Water, formaldehyde and impurities are distilled together.
    [68] As a modification, steam may be directly passed through the solution to be distilled.
    [69] Separation of impurities such as formaldehyde and ethyl acrolein from the aldol product by steam distillation is preferably carried out under a vacuum or an atmospheric pressure at a temperature of 50 to 110 ° C.
    [70] The unreacted formaldehyde separated from the aldol product is refluxed back into the aldol reactor thereby reducing formaldehyde consumption and increasing the efficiency of the overall process.
    [71] As a hydrogenation catalyst, a commercially available catalyst such as a supporting metal catalyst may be used by constituting Cu, Cr, Ni, Zn, Pt, Pd, Ru, Mn or Cu.
    [72] A suitable catalyst is a Cu-Zn / Al 2 O 3 , Cu-Cr / Al 2 O 3, Ni-Cr / SiO 2, Pt / C, Pt-Pd / C, Ru / C and Ru-Pt / C Preferred catalysts include Cu-Cr / Al 2 O 3 and Ni-Cr / SiO 2 .
    [73] The Ni content of the catalyst is 60-99 wt%, and the Cr content is 1-40 wt%.
    [74] When the reaction mixture contains formaldehyde in the aldolization step and the hydrogenation step is carried out in water, the choice of Ni-catalyst is preferred.
    [75] The catalyst may be an inorganic oxide such as silica or a carrier suitable for carbon.
    [76] The catalyst can be selectively activated in a hydrogen flow, preferably at a temperature of about 400 < 0 > C, prior to the hydrogenation reaction.
    [77] The hydrogenation reaction step can be carried out as a batch process, as a semi batch process, or preferably as a continuous process.
    [78] After the hydrogenation step, certain desired polyols are separated in the reaction mixture by suitable methods, such as distillation, and the solvent used can be refluxed to the hydrogenation step.
    [79] The method according to the invention has several advantages.
    [80] The aldolization reaction is carried out using a solid phase catalyst, so that there is no need to separate the catalyst and recycle the catalyst after the reaction.
    [81] In the process for producing the polyol, since water is the optimum amount in the aldolization reaction step, it exhibits excellent conversion rate and improved selectivity.
    [82] In the case of 1,1,1-trimethylolpropane, the production of ethyl acrylate can be reduced by optimizing the amount of water in the reaction mixture.
    [83] The use of water as a solvent in the hydrogenation reaction step improves the performance of the hydrogenation reaction because the catalytic inhibitory effect of formaldehyde does not occur more than expected and the hydrogenation catalyst is less needed.
    [84] This method is very effective, and the cost is low.
    [85] The reason for this is that complete elimination of formaldehyde is not required after the aldolization reaction step, and in the hydrogenation treatment in water, smaller amounts and larger amounts of formaldehyde work in the same way.
    [86] The selectivity of the aldolization reaction step in the presence of the weakly basic anion exchange resin, the performance in the hydrogenation step and the yield of the coarse product can be reduced and effectively improved by the process of the present invention.
    [87] This is because the consumption of raw materials can be reduced and the purification cost of the final product can be reduced.
    [88] Next, the present invention will be described more specifically with reference to Examples, but the present invention is not limited thereto.
    [89] Examples 1-7 Aldolisation < RTI ID = 0.0 >
    [90] Seven kinds of experiments were conducted using formaldehyde and n-butyraldehyde as starting materials.
    [91] The effect of solvent or bisolvent on the aldolization reaction was investigated using water concentrations of different methanol in the feed mixture.
    [92] Experimental conditions and results of the aldolization reaction are shown in Table 1 below.
    [93] Table 1 Experimental Conditions and Results of Aldolization
    [94]
    [95] Note: In the examples without methanol, formaldehyde was introduced into the system as paraformaldehyde, and 42 wt% formaldehyde was used in the example using methanol.
    [96] Therefore, the amounts shown in Table 1 are the amounts used for paraformaldehyde in Examples 1-5 and formalin in Examples 6 and 7.
    [97] Paraformaldehyde in Examples 4 and 5 contains 25 wt% water.
    [98] F11: Formaldehyde
    [99] BAL: n-Butyraldehyde
    [100] TMPA: 2-ethyl-3-hydroxy-2 '- (hydroxymethyl) propanal
    [101] EA: ethyl acrolein
    [102] * Commercial anion exchange resins were used in each example.
    [103] Examples 8-16
    [104] Several commercially available anion exchange resins were tested as aldolization catalysts.
    [105] Important resin properties are listed in Table II below.
    [106] The selectivity value (S) for the aldol, defined as the ratio of aldol yield to ethyl acrolein yield, is shown in Table II.
    [107] Examples 8 to 16 were carried out at a temperature of 60 DEG C at a ratio of formaldehyde to butyraldehyde of 4: 1.
    [108] The results obtained were calculated after 6 hours of reaction time.
    [109] Table Ⅱ Anion exchange resin used as an aldolization catalyst
    [110]
    [111] Na: Can not process (NoT Applicable)
    [112] Example 17 Aldol product The purification of 2-ethyl-3-hydroxy-2- (hydroxymethyl) propanol
    [113] Formaldehyde was isolated from the aldol product at atmospheric pressure at 100 占 폚 using 400 ml of a total batch volume (volume of 200 ml of distilled water and 200 ml of aldolization reaction product).
    [114] Excess water was added immediately after observing the distillate droplets first obtained from the condenser.
    [115] The water was adjusted to maintain a constant solution volume in the distillation flask.
    [116] In order to reduce formaldehyde content from 4.5 wt% to 1.0 wt% or less, 750 mL of water supplied through a distillation pot was required.
    [117] The distillation time was 3 hours.
    [118] In order to reduce formaldehyde content to 0.2 wt% or less, 1600 mL of water supplied through the distillation pot was required, and the distillation time was 7 hours.
    [119] After the distillation, 200 ml of water was evaporated in the solution to remove water added before distillation.
    [120] The dominant co-product, ethyl acrolein, obtained in the aldolization reaction step was distilled off in the separation step.
    [121] Example 18-19 Hydrogenation of purified aldol product obtained by 1,1,1-trimethylol propane (1,1,1-trihydroxymethylpropane)
    [122] Two examples were conducted using 0.19 wt.% And 0.93 wt.% Of different formaldehyde concentrations in the feed mixture.
    [123] These examples were carried out in a pressurized batch reactor connected with a bubbling unit.
    [124] 5 g of commercially available Ni-catalyst was charged into the reactor and the hydrogen flow was adjusted to 500 ml / mix at a pressure of 2 bar.
    [125] After a certain desired activation temperature (400 ° C) was reached, the hydrogen gas flow was increased to 750 ml / min to activate the catalyst.
    [126] Formaldehyde and ethyl acrolein were then separated from 150 ml aldol product and mixed with 150 ml methanol.
    [127] The feed mixture was injected into the foaming device to saturate oxygen to remove it from the solution.
    [128] The pressure in the reactor was reduced from 2 bar to 1.5 bar while the pressure in the foaming device was increased to 8 bar and the feed mixture was injected into the reactor.
    [129] The hydrogen feed was introduced by adjusting the desired desired pressure (70 bar) and temperature (90 ° C).
    [130] When the temperature became 15 to 20 占 폚 or less at a predetermined temperature, stirring was performed to adjust the temperature to 1000 rpm.
    [131] Samples taken in this treatment step were analyzed by HPLC and GC.
    [132] The operating conditions and results obtained in these examples are summarized below.
    [133] Example 18
    [134] Catalyst: Commercial Ni-catalyst
    [135] Particle size: 45 ~ 150㎛
    [136] Catalyst weight: 5 g
    [137] Solution volume: 300 ml
    [138] Temperature: 90 ° C
    [139] Pressure: 70 bar
    [140] Stirring speed: 1000 rpm
    [141] Feed mixture: formaldehyde 0.19 wt%
    [142] Aldol product 14.55 wt%
    [143] MeOH + H 2 O 85.26 wt%
    [144] Product: 1,1,1-trimethylol propane 14.67 wt%
    [145] MeOH + H 2 O 85.33 wt%
    [146] Conversion rate: 100%
    [147] Selectivity: 99%
    [148] Example 19
    [149] Catalyst: Commercial Ni-catalyst
    [150] Particle size: 45 ~ 150㎛
    [151] Catalyst weight: 5 g
    [152] Solution volume: 300 ml
    [153] Temperature: 90 ° C
    [154] Pressure: 70 bar
    [155] Stirring speed: 1000 rpm
    [156] Feed mixture: 0.93 wt% formaldehyde
    [157] Aldol product 13.14 wt%
    [158] MeOH + H 2 O 85.93 wt%
    [159] Product: 1,1,1-trimethylol propane 12.15 wt%
    [160] MeOH + H 2 O + uic 87.85 wt%
    [161] (uic: unidentified component)
    [162] Conversion rate: 100%
    [163] Selectivity: 91%
    [164] In Example 18 carried out with an extremely low formaldehyde content (< 0.2 wt%), the rate of hydrogenation was significantly higher at the beginning and no inhibition was observed.
    [165] This shows that there is a strong inhibitory effect of aldehyde, which can be seen in the following graph 3.
    [166] The initial inhibition at a reaction rate of temperature 90 DEG C was observed when the formaldehyde content in the feed was 0.93 wt% (Example 19).
    [167] Graph 3
    [168] The formaldehyde concentration of Example 19 was 0.93 wt% (- -) and a formaldehyde concentration of 0.2 wt% or less (- -), the hydrogenation effect of aldol at 90 ℃ and 70 bar
    [169]
    [170] Effect of Solvent by Hydrogenation of TMP-Aldol
    [171] Examples 20-26
    [172] First, a commercially available Ni-catalyst having a sieving (particle size < 45 mu m) was pulverized and activated in a hydrogen gas flow at 400 DEG C for 1 hour.
    [173] The hydrogenation feed was then introduced into the foaming device and saturated with hydrogen in 10 minutes to remove oxygen from the resulting solution.
    [174] After removing the oxygen, the reaction mixture was introduced into an autoclave.
    [175] When the desired pressure and temperature values were obtained by adjusting the pressure and temperature, the stirring speed was adjusted by a magnetic stirrer.
    [176] Liquid samples were collected and analyzed.
    [177] The superiority of pure water as a solvent when using high formaldehyde (FH) content is shown in graphs 4 and 5.
    [178] In Examples 24 to 26, hydrogenation was carried out under different treatment conditions using water as a solvent.
    [179] The processing conditions and results of the embodiment are summarized below.
    [180] Examples 20 to 23 Preparation of water and methanol as a solvent in the hydrogenation reaction
    [181] Example 20 (methanol solvent)
    [182] Catalyst: Commercial Ni-catalyst
    [183] Particle size: <45㎛
    [184] Catalyst weight: 5 g
    [185] Solution volume: 300 ml
    [186] Temperature: 80 ° C
    [187] Pressure: 80 bar
    [188] Stirring speed: 1500 rpm
    [189] Feed mixture: FH 2.17 wt%
    [190] TPM-aldol 9.90 wt%
    [191] TPM 1.03wt%
    [192] MeOH 42.0 wt%
    [193] H 2 O 44.9 wt%
    [194] Product: TMP 7.44 wt%
    [195] TPM-aldol 4.04 wt%
    [196] FH 0.04 wt%
    [197] MeOH * 43.6 wt%
    [198] H 2 O 44.9 wt%
    [199] Conversion rate (360 minutes): 59%
    [200] Selectivity: 100%
    [201] Example 21 Non-methanol Solvent
    [202] Catalyst: Commercial Ni-catalyst
    [203] Particle size: <45㎛
    [204] Catalyst weight: 5 g
    [205] Solution volume: 300 ml
    [206] Temperature: 80 ° C
    [207] Pressure: 80 bar
    [208] Stirring speed: 1500 rpm
    [209] Feed mixture: FH 2.27 wt%
    [210] TPM-aldol 11.11 wt%
    [211] TPM 0.68wt%
    [212] MeOH 0.3 wt%
    [213] H 2 O 85.64 wt%
    [214] Product: TMP 12.74 wt%
    [215] TPM-aldol 0wt%
    [216] FH 0wt%
    [217] MeOH * 1.6 wt%
    [218] H 2 O 85.64 wt%
    [219] Conversion Rate (360 minutes): 100%
    [220] Selectivity: 100%
    [221] * MeOH: Metal alcohol produced from hydrogenation of FH
    [222] Graph 4
    [223] Hydrogenation of TMP-aldol at 80 ° C and 80 bar with high FH content (over 2 wt%) using a mixture of methyl alcohol and H 2 O or pure water as solvent
    [224]
    [225] Example 22 Methanol Solvent
    [226] Catalyst: Commercial Ni-catalyst
    [227] Particle size: 45 ~ 150㎛
    [228] Catalyst weight: 5 g
    [229] Solution volume: 300 ml
    [230] Temperature: 90 ° C
    [231] Pressure: 80 bar
    [232] Stirring speed: 1500 rpm
    [233] Feed mixture: FH 0.99 wt%
    [234] TPM-aldol 12.18 wt%
    [235] TPM 0.87 wt%
    [236] MeOH 85.96 wt% 50% MeOH
    [237] 35.96% H 2 O
    [238] Product: TMP 13.5 wt%
    [239] MeOH + H 2 O 86.5 wt%
    [240] Conversion rate (120 min): 100%
    [241] Selectivity: 100%
    [242] Example 23 Non-methanol Solvent
    [243] Catalyst: Commercial Ni-catalyst
    [244] Particle size: 45 ~ 150㎛
    [245] Catalyst weight: 5 g
    [246] Solution volume: 300 ml
    [247] Temperature: 90 ° C
    [248] Pressure: 80 bar
    [249] Stirring speed: 1500 rpm
    [250] Feed mixture: FH 0.63 wt%
    [251] TPM-aldol 10.80 wt%
    [252] TPM 1.22 wt%
    [253] H 2 O 87.35 wt%
    [254] Product: TMP 12.50 wt%
    [255] H 2 O + MeOH * 87.5 wt%
    [256] Conversion Rate (50 min): 100%
    [257] Selectivity: 100%
    [258] * MeOH is MeOH generated from the hydrogenation of FH.
    [259] Graph 5
    [260] Hydrogenation of TMP-aldol with low FH initial content (1 wt% or less) at 90 ° C and 80 bar pressure using a mixture of MeOH and H 2 O as a solvent or pure water
    [261]
    [262] EXAMPLES 24-26 Under different operating conditions, water
    [263] Example 24 Non-methanol Solvent
    [264] Catalyst: Commercial Ni-catalyst
    [265] Particle size: 45 ~ 150㎛
    [266] Catalyst weight: 5 g
    [267] Solution volume: 300 ml
    [268] Temperature: 90 ° C
    [269] Pressure: 80 bar
    [270] Stirring speed: 1500 rpm
    [271] Feed mixture: FH 2.25 wt%
    [272] TPM-aldol 10.83 wt%
    [273] TPM 0.95 wt%
    [274] H 2 O 85.97 wt%
    [275] Product: TMP 12.35 wt%
    [276] 0.13 wt% TMP-
    [277] H 2 O + MeOH * 87.52 wt%
    [278] * MeOH is MeOH generated from the hydrogenation of FH.
    [279] Conversion rate (290 minutes): 99%
    [280] Selectivity: 100%
    [281] EXAMPLES Non-methanol Solvent
    [282] Catalyst: Commercial Ni-catalyst
    [283] Particle size: 45 ~ 150㎛
    [284] Catalyst weight: 5 g
    [285] Solution volume: 300 ml
    [286] Temperature: 75 ° C
    [287] Pressure: 60 bar
    [288] Stirring speed: 1500 rpm
    [289] Feed mixture: FH 0.63 wt%
    [290] TPM-aldol 10.78 wt%
    [291] TPM 1.24wt%
    [292] H 2 O 87.37 wt%
    [293] Product: TMP 12.48 wt%
    [294] 0.15 wt% TMP-
    [295] H 2 O + MeOH * 87.37 wt%
    [296] Conversion rate (80 min): 99%
    [297] Selectivity: 100%
    [298] * MeOH is MeOH generated from the hydrogenation of FH
    [299] Example 26 Non-methanol Solvent
    [300] Catalyst: Commercial Ni-catalyst
    [301] Particle size: 45 ~ 150㎛
    [302] Catalyst weight: 5 g
    [303] Solution volume: 300 ml
    [304] Temperature: 60 ° C
    [305] Pressure: 40 bar
    [306] Stirring speed: 1500 rpm
    [307] Feed mixture: FH 0.62 wt%
    [308] TPM-aldol 11.20 wt%
    [309] TPM 1.18 wt%
    [310] H 2 O 87.0 wt%
    [311] Product: TMP 12.7 wt%
    [312] H 2 O + MeOH * 87.3 wt%
    [313] Conversion Rate (230 min): 100%
    [314] Selectivity: 100%
    [315] * MeOH is MeOH generated from the hydrogenation of FH.
    [316] According to the present invention, it is possible to effectively and industrially synthesize polyols having three or four hydroxyl groups such as trimethylolethane, trimethylolpropane and pentaerythritol.
    [317] By the method of the present invention, a known process such as an aldolization reaction following the Kaniza reaction is substituted, and an aldolization reaction is included after the hydrogenation step.
    [318] A starting material in the production of a synthetic resin such as a polyester resin and a polyol as an intermediate can be obtained at low cost by the present invention.
    权利要求:
    Claims (11)
    [1" claim-type="Currently amended] In the process for preparing a polyol having 3 or 4 hydroxy groups by hydrogenation of aldehydes, the aldehyde is reacted with at least two -Hydrogen atoms and an aldehyde having the formula R 1 CH 2 CHO with formaldehyde and weakly basic An anion exchange resin in the presence of 48 to 65 wt% of water at a temperature of 50 to 100 DEG C and the hydrogenation reaction is carried out at a temperature of 50 to 200 DEG C in the presence of 0 to 90 wt% &Lt; / RTI &gt;
    Gastric ROneCH2In CHO, ROne Lt; RTI ID = 0.0 &gt; C, &lt; / RTI &gt; optionally substituted with at least one cycloalkyl substituent,One-C7An alkyl group, a cycloalkyl group, an aryl group, and an aralkyl group having 1 to 7 carbon atoms in the alkyl chain thereof.
    [2" claim-type="Currently amended] The method according to claim 1,
    The weakly basic anion exchange resin comprises a primary amine having a -NH 2 group, a secondary amine having an -NHR group (wherein R is an alkyl or aryl group), a tertiary amine having a -N (R) 2 group, Each of which is an alkyl group or an aryl group) and / or a mixture thereof.
    [3" claim-type="Currently amended] The method according to claim 1,
    Wherein the hydrogenation reaction is carried out in the presence of a hydrogenation reaction catalyst comprising Ni, Cu, Cr, Zn, Pt, Pd, Ru, Co and / or Mn.
    [4" claim-type="Currently amended] The method of claim 3,
    Characterized in that the hydrogen-participating reaction catalyst is supported on a carrier.
    [5" claim-type="Currently amended] 5. The method of claim 4,
    Wherein the carrier is an inorganic oxide or carbon.
    [6" claim-type="Currently amended] The method according to claim 1,
    Wherein the hydrogenation reaction is carried out at a temperature of 60 to 90 占 폚.
    [7" claim-type="Currently amended] The method according to claim 1,
    Wherein the hydrogenation reaction is carried out in the presence of Ni-catalyst and 20-90 wt% of water.
    [8" claim-type="Currently amended] The method according to claim 1,
    Wherein the aldehyde comprising at least two -Hydrogen atoms is n-butanal, propanal or acetaldehyde.
    [9" claim-type="Currently amended] The method according to claim 1,
    Wherein the aldehyde obtained in the aldolization reaction is subjected to steam distillation before the hydrogenation reaction.
    [10" claim-type="Currently amended] 10. The method of claim 9,
    Characterized in that the steam distillation is carried out at sub-atmospheric pressure.
    [11" claim-type="Currently amended] 11. The method according to claim 9 or 10,
    Wherein the steam distillation is carried out in a vacuum state.
    类似技术:
    公开号 | 公开日 | 专利标题
    JP4889859B2|2012-03-07|Processes for the purification of alkyl alkanoates
    US6201160B1|2001-03-13|Preparation of alcohols
    KR101218414B1|2013-01-03|co-production of vinyl acetate and ethyl acetate
    EP1172349B1|2005-04-20|Multi-step process for the preparation of oxo-aldehydes and/or alcohols
    ES2233077T3|2005-06-01|Procedure for the preparation of ethyl acetate.
    US6680414B2|2004-01-20|Process for the hydrogenation of hydroformylation mixtures
    EP0987242B1|2002-12-04|Process for the preparation of higher oxo-alcohols from olefin mixtures
    CN1165504C|2004-09-08|Selective hydrogenation process of hydrogenation formylation mixture
    EP0003858B1|1981-07-15|A process for selectively removing minor amounts of beta-chloroacroleins and 5,6-epoxyhexene-1 from epichlorohydrin
    DK167183B1|1993-09-13|Procedure for preparing alcohols by steam phase hydrogenation of aldehydes
    US3000906A|1961-09-19|Purification of pivalolactone
    RU2330032C2|2008-07-27|Method of purifying crude propene-oxide
    KR100814310B1|2008-03-18|Process for the epoxidation of olefins
    EP0572812B1|1996-03-13|Method of producing 1,3-propanediol, by hydrogenation of hydroxypropionaldehyde
    US4122290A|1978-10-24|Process for the preparation of trimethylolalkanes
    US8562921B2|2013-10-22|Ethyl acetate production
    US6187971B1|2001-02-13|Method for producing polyalcohols
    EP2417089B1|2013-06-05|Method for producing 1,6-hexanediol and caprolactone
    ES2201334T3|2004-03-16|Procedure for the preparation of polivalent alcohols.
    KR101582107B1|2016-01-04|Method of producing neopentyl glycol
    EP2385933B1|2014-06-25|Method for producing polymethylols
    EP0343475B1|1993-08-04|Process for producing neopentyl glycol
    KR100463360B1|2005-02-28|Process for the Preparation of Polyalcohols
    US5004845A|1991-04-02|Hydrogenation of aldehydes
    CA1051039A|1979-03-20|Process for the production of butanediol
    同族专利:
    公开号 | 公开日
    US20020151754A1|2002-10-17|
    AU5831500A|2001-01-22|
    KR100636869B1|2006-10-19|
    SA1549B1|2006-11-11|
    AR032745A1|2003-11-26|
    DE60008559D1|2004-04-01|
    EP1218328B1|2004-02-25|
    FI991519A|2001-01-03|
    FI109993B1|
    EP1218328A1|2002-07-03|
    JP2003503470A|2003-01-28|
    WO2001002330A1|2001-01-11|
    ES2211567T3|2004-07-16|
    CN1217900C|2005-09-07|
    DE60008559T2|2004-12-16|
    FI109993B|2002-11-15|
    AT260230T|2004-03-15|
    US6593502B2|2003-07-15|
    TW541296B|2003-07-11|
    CN1360562A|2002-07-24|
    JP3868294B2|2007-01-17|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1999-07-02|Priority to FI991519
    1999-07-02|Priority to FI991519A
    2000-06-30|Application filed by 다이니아 케미컬스 오이
    2002-05-30|Publication of KR20020040682A
    2006-10-19|Application granted
    2006-10-19|Publication of KR100636869B1
    优先权:
    申请号 | 申请日 | 专利标题
    FI991519|1999-07-02|
    FI991519A|FI109993B|1999-07-02|1999-07-02|A process for preparing polyols|
    [返回顶部]