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    • 专利摘要:
    The present invention provides a process for the preparation of zeolites X and LSX in which about 50 to about 99% of the exchangeable sites are agglomerated with a binder filled with lithium ions, comprising exchanging a portion of the exchangeable cations of the starting zeolite with lithium, The exchange consists of contacting the zeolite distributed in two or more vessels in a static bed form, arranged in series, in a mutually changeable manner, with the lithium compound solution 1 being transported through the carousel, The sequence of vessels is adjusted cyclically at a given time interval; When lithium is exchanged in the first vessel by the desired amount in the zeolite, the first vessel is removed from the series of carousels, the zeolite present in it is washed to remove the solution of the lithium compound and discharged (4) Exchanged with a fresh zeolite charge to be optionally exchanged, the bleed 5 being separated from the effluent generated by the carousel and discharged from the stream corresponding to the excess of lithium used and The first stream 5 corresponding to filtration "e" at the outlet of the head column of the carousel Subsequent stream (3) corresponding to the filtration "E 0 " at the outlet of the carousel. (“E 0 ” is the stoichiometric equivalent of exchangeable lithium in a sieve and “e” is the excess required to obtain the desired degree of exchange for lithium, preferably greater than 96%) in the carousel Discharged It is related with the manufacturing method of X type zeolite characterized by the above-mentioned. The method makes it possible to achieve a high level of lithium exchange with significantly improved lithium yield over the prior art methods.
    公开号:KR20020005495A
    申请号:KR1020010040542
    申请日:2001-07-06
    公开日:2002-01-17
    发明作者:마시니쟝-쟈끄；쁠레도미니끄；사끌뢰쟝-끌로드；비달쟝-루이
    申请人:쇼송 빠뜨리시아；세카 에스. 에이.；
    IPC主号:
    专利说明:

    PROCESS FOR THE PREPARATION OF AGGLOMERATED ZEOLITES X AND LSX EXCHANGED WITH LITHIUM
    [2] The present invention relates to a process for the preparation of agglomerated zeolites of type X wherein some of the exchangeable cationic sites are filled with lithium ions.
    [3] The term “zeolite of type X” is understood to mean zeolite X with an Si / Al atomic ratio of 1.5 and more particularly zeolite LSX (Low Silica X) having an Si / Al atomic ratio of about 1 as follows.
    [4] Zeolite X exchanged with lithium (i.e., at least part of the cationic exchangeable site is filled with lithium ions) has many industrial applications, and the selective adsorption technique of the gas to be separated allows nitrogen to be transferred to other gases, for example Widely used to separate from oxygen, argon and hydrogen. The zeolites used can be provided in a variety of forms, and the very form employed can determine their usefulness in industrial adsorption methods. When zeolites are used as industrial adsorbents, in order to avoid the risk of compacting or at least significantly reducing the stream in the column by compacting the zeolites in powder form in industrial scale adsorption columns, for example, by converting them into particulates It is desirable to form aggregates.
    [5] According to US Pat. No. 3,140,933, the X-type zeolite in which the base ions are exchanged with lithium ions can be effectively used to separate nitrogen from oxygen in the temperature range up to 30 ° C. Since the exchange of ions is not total and zeolite X has been synthesized in sodium medium, the adsorbent used is mixed sodium / lithium zeolite.
    [6] US 4,859,217 discloses the separation of nitrogen from oxygen by adsorption at temperatures of 15 to 70 ° C., using zeolite X-type containing more than 88% of ions of lithium ions, especially when the zeolite is used with an atomic ratio of Si / Al of 1 to 1.25. Discloses that is very good.
    [7] US 5,179,979 has a higher thermal stability than the corresponding zeolites having only lithium, the X-type lithium / alkaline earth metal zeolites having a molar ratio of lithium / alkaline earth metal of about 95/5 to 50/50, and having good adsorption selectivity and capacity. Insist.
    [8] US 5,152,813 has a Si / Al zeolite ratio ≦ 1.5, the exchangeable site is filled with at least 2 ions (5 to 95% lithium ions, and a second ion selected from 5 to 95% calcium, strontium and mixtures thereof) ), A method of adsorbing nitrogen in a gas mixture wherein the sum (lithium and the second exchangeable ion) is at least 60%.
    [9] US 5,464,467 has a cation equivalent of about 50 to about 95% lithium, aluminum, scandium, gallium, iron (III), chromium (II), indium, yttrium, lanthanide alone or two or more lanthanide mixtures, and mixtures thereof About 4 to about 50% selected trivalent ions and 0 to about 15% residual ions selected from sodium, potassium, ammonium, hydronium, calcium, strontium, manganese, barium, zinc, copper (II) and mixtures thereof And a type X zeolite, which is prepared by first exchanging a replaceable cation of a zeolite previously agglomerated with a binder, followed by exchange with a trivalent cation or cations.
    [10] US 5,932,509 discloses the same zeolite in such a way that it consists first of exchanging the exchangeable cation of the zeolite X powder with a trivalent cation, then coagulating with a binder, and finally performing an exchange of lithium on the coagulated zeolite. The manufacturing method to manufacture is shown. The method requires drying of the zeolite material and intermediate activation. However, there is an advantage of limiting the loss of expensive end products due to the amount of lithium by performing final lithium exchange on the product produced by particle separation.
    [11] Because of the high cost of lithium salts, it is necessary to use alternative lithium exchange methods where possible to avoid loss of lithium.
    [12] EP 863,109 is a series of two or more vessels in which ions, in particular lithium ion exchange solutions, are arranged so that they can be periodically exchanged around and the exchange solution filled with the zeolites to be exchanged is in each case transferred from a series of first vessels to the next. When passing through and reaching the desired level of ion exchange, the vessel containing the zeolite exchanged to the desired level is separated in a series of devices and the exchange solution is separated from the zeolite, washed, purified and re-substituted zeolite Disclosed is a continuous countercurrent process of zeolite ion exchange in the form of zeolites, preferably in particulate form, which is replaced with The method is a zeolite that is highly exchanged with lithium, i.e. has a high degree of lithium exchange (corresponding to the Li / Li + Na molar ratio of Li and Na ions in the zeolite), but the output of lithium is very poor (i.e. 12% or less). By making it possible to obtain the solution, this process cannot be industrially carried out in which the solution recovered at the outlet of a vessel comprising a lithium-exchanged zeolite contains not only lithium but also ions, usually sodium and / or potassium, which have been exchanged. As a cumbersome reprocessing is required before release to the environment can be made, it is difficult to effectively recover the solution industrially.
    [13] The present invention provides a process for the preparation of zeolite X aggregates in which at least some of the exchangeable sites are filled with lithium and do not exhibit the disadvantages of the process in the prior art described above.
    [1] 1, (1) is a lithium compound solution, (2) is an effluent, (3) is a second stream, (4) is a separation of the head column and delivery of its filler, (5) is a first stream Where H is the head column, M is the middle column, and T is the tail column.
    [14] The above-mentioned zeolites prepared according to the method which is the subject of the present invention contain the following ones having an atomic ratio of Si / Al of 1.5 or less, preferably 0.9 to 1.1, and exchangeable cations represented by equivalent weight, and coagulating with a binder. Is a type X zeolite;
    [15] About 50 to about 99% and preferably at least 96% of lithium ions,
    [16] Trivalent ions selected from aluminum, scandium, gallium, iron (III), chromium (III), indium, yttrium, lanthanide or rare earth metals alone or in mixtures, and / or calcium, strontium, zinc, copper, chromium (II) About 4 to about 50% of a divalent ion selected from iron (II), manganese, nickel or cobalt alone or in a mixture,
    [17] 0 to about 15% residual ions selected from sodium, potassium, ammonium or hydronium alone or in a mixture, agglomerated with a binder.
    [18] The process according to the invention not only has a final level of lithium exchange of at least 96%, but also an improved output than EP 863,109, ie an easier treatment of lithium containing effluents for effective recovery purposes, resulting in a yield of at least 45% and in the zeolites obtained The concentrations of Li, Na, and K are represented by Li, Na, and K, respectively, and the ratio of the amount of lithium fixed to the zeolite to the amount of lithium introduced is defined as the Li / Li + Na + K ratio. It is characterized by the fact that it is possible to obtain a lithium yield of at least 80%.
    [19] Coagulation
    [20] The first step of the method developed by the Applicant consists of coagulating the starting zeolite with an inert binder. As starting zeolites, zeolite X powders, which are generally obtained by synthesis, whose main exchangeable sites are mainly filled with sodium and / or potassium ions, are generally used.
    [21] Some of the sodium and / or potassium cations are calcium, strontium, zinc, copper, chromium (II), iron (II), manganese, nickel, cobalt, aluminum, scandium, gallium, iron (III), chromium (III), indium Zeolites substituted with one or more divalent and / or trivalent cations such as yttrium or lanthanide or rare earth metals may also be used.
    [22] The exchangeable cationic sites of the zeolites are more suitable for use in high speed mixers, whereby the solution of the zeolite suspension and compound to be exchanged is preferably reliably homogeneously mixed with the suspension and the solution after a short contact time (minutes) of the solution. The zeolites, preferably in the form of water-soluble suspensions, are preferably trivalent ions and / or divalent ions by simultaneously pumping into a static mixer which is able to ensure a homogeneous mixing of the solution after a very short contact time (seconds). Contact with a solution of the compound of causes the divalent and / or trivalent ions or ions to exchange on the starting sodium or sodium + potassium zeolite. At this time, all the batches are made such that the flow rate is adjusted so that the weight ratio of the weight of the suspension to the solution is substantially constant.
    [23] If the mixture obtained is aged with gentle stirring of about 1 hour, the willingness to exchange in the static mixer for the degree of exchange retaining the quantitative degree achieved by normal exchange is ineffective. It has been found that better random distribution of divalent and / or trivalent ions in the zeolite structure is obtained, which is manifested by a markedly improved final level of nitrogen absorption capacity, which is unexpected.
    [24] Although this is not absolutely necessary, it is preferable to use an aqueous solution of exchange ions (bivalent and / or trivalent ions). Any water soluble compound of exchange ions can be used. Preferred water-soluble compounds of ions are salts, in particular chlorides, sulfates and nitrates. Particularly preferred salts are chlorides because of their high solubility and easy availability.
    [25] When it is desired to produce a zeolite in which part of the cationic site is filled with several types of divalent and / or trivalent ions as defined above, all cations are brought into contact with a solution containing all of these cations to simultaneously It is possible to exchange, to exchange each cation in succession, or to employ an intermediate solution between two preceding solutions.
    [26] Another preferred form consists of exchanging exchangeable cations or cations of zeolites simultaneously with trivalent and / or divalent ions and monovalent ions, preferably sodium ions.
    [27] Another preferred alternative form may or may not be combined with any of the above preferred forms, immediately after exchange with trivalent and / or divalent ions, or simultaneously with trivalent and / or divalent and monovalent ions. And then immediately stabilizes the zeolite with sodium hydroxide.
    [28] In a method known to those skilled in the art, after each step of ion exchange, the zeolite is washed with water and then dried at a temperature generally between 40 and 200 ° C.
    [29] When trying to obtain a zeolite aggregate exchanged at a high level, usually at least 96%, relative to lithium, very large amounts, even all, of the exchangeable cations of the starting zeolite or of the preaggregated zeolites, are all monovalent cation species, preferably Preferably it is converted to sodium or ammonium ion form. To this end the zeolite is contacted with a solution comprising monovalent ions such as sodium or ammonium ions, such as an aqueous solution of NaCl (preferably) or NH 4 Cl before or after the flocculation step. The inventors have found that the exchange step facilitates the purification process and reduces the lithium exchange by reducing excessive "e".
    [30] Prior to lithium exchange, the degree of exchange with respect to the potassium of the zeolite is preferably 15% or less, advantageously 10% or less of the total exchangeable sites.
    [31] For the agglomeration, in the first step, the starting zeolite X mentioned is generally mixed in the presence of water in the form of a binder in powder form, and then the mixture is converted into agglomerates, for example, by injection or bead molding, and the molded zeolite The / binder mixture is heated at a temperature of about 400-700 ° C., converting to “green” aggregates that are resistant to grinding. Binders used to agglomerate zeolites include clay (especially preferred by Applicant's company), silica, alumina, metal oxides and mixtures thereof.
    [32] It is possible to produce agglomerates containing less than 5% by weight of the residual binder. The process for preparing such aggregates with low levels of binder consists in converting the binder of the aggregates described above to the zeolite phase. For this purpose, the starting point is the agglomeration of the zeolite X powder with a zeolite convertible binder (for example kaolin or metakaolin), after which the conversion to zeolite is followed by alkali mash, for example according to the method disclosed in EP 932,581. This is done using maceration. In this way, it is possible to easily obtain very effective particulates which exhibit 95% or more of zeolite according to the invention.
    [33] In addition, the zeolite is a three component composition such as silica / alumina / toria, silica / alumina / zirconia as binder, as well as silica / alumina, silica / magnesia, silica / zirconia, silica / toria, silica / beryllium oxide and silica / titanium dioxide And agglomerates with materials such as clay.
    [34] The relative ratios of the constituents of the binder and zeolite can vary widely. Aggregate binders are generally present at 5 to 30 parts by weight per 100 parts by weight of the flocculated material. It is advantageous for the aggregate to have a diameter of about 0.2 to about 5 mm.
    [35] An alternative form of the flocculation step for zeolites in which part of the exchangeable cationic sites is filled with divalent and / or trivalent cations is, firstly, sodium or sodium before exchanging some of the sodium and optionally some of the potassium of the zeolite. + Potassium zeolite first and then coagulate with divalent and / or trivalent cations.
    [36] Li exchange
    [37] For agglomerated zeolites, according to the method described in detail below, agglomerated zeolites, preferably in the form of water-soluble suspensions, are contacted with an aqueous solution of a lithium compound (1) solution, preferably a lithium salt such as LiCl Exchange at least a portion of the exchangeable cations of the zeolite.
    [38] The agglomerated zeolites to be exchanged (for simplicity in the following, the exchangeable cations are regarded as only Na and K) have at least two, preferably three, lithium solution solutions arranged in a series and interchangeable manner. It is distributed to the container of the static bed form mentioned above, and is transported through the said container arranged in series. In the above, a sequence of serially arranged vessels, known as carrousels, is controlled periodically at a given time interval, and the inlet of fresh solution is the first vessel in which the zeolite exchanged with lithium to the maximum extent is found in each case. Go to the next container in the series. When lithium is exchanged in the first vessel by the desired amount in the zeolite, the first vessel is removed from the series of carousels, the zeolite present in it is washed, removed from the solution of the lithium compound and discharged (4), Replace with fresh zeolite charge to be optionally exchanged.
    [39] The process according to the invention separates the bleed 5 from the effluent generated by the carousel, and the excess amount of lithium used (hereinafter, for simplicity, regards the lithium compound solution used as an aqueous LiCl solution). And discharged from the stream corresponding to the discharged from the carousel:
    [40] The first stream 5 corresponding to filtration "e" at the outlet of the head column of the carousel
    [41] Subsequent stream (3) corresponding to the filtration "E 0 " at the outlet of the carousel.
    [42] (“E 0 ” is the stoichiometric equivalent of exchangeable lithium in a sieve and “e” is the excess required to obtain the desired degree of exchange (surprisingly greater than 96%)).
    [43] This results in two streams:
    [44] The first stream 5 or bleed (outlet of the first vessel) is in effect a LiCl solution containing trace amounts of NaCl and KCl.
    [45] The second stream 3 (outlet of the carousel) is rich in NaCl and KCl and contains a reduced amount of LiCl, which has the advantage of being released into the natural environment with a simple purification treatment for lithium.
    [46] The diagram shown in the accompanying drawings corresponds to the method according to the invention described above.
    [47] The method according to the invention consists of three steps:
    [48] 1-As an initial start-up of the carousel, its action is to filter the lithium chloride solution 1, thereby placing a column system on a column of carousel filled with starting zeolite at the Li exchange level, so that the method Consists of allowing inflow to carousel,
    [49] 2-normal action (how to obtain a totally stable result over each cycle following the same procedure as described above)
    [50] 3-End of cycle.
    [51] In a preferred case in which the plant operates with three columns, the initial start up step may also consist of:
    [52] In the first and second places of the exchange line, install two pre-exchanged columns obtained at the end of the previous compilation, and install columns of "virgin" beads in the tail position; In this case, starting requires a low Li consumption which is substantially the same as for the normal cycle in normal operation;
    [53] Or, start with three columns of "new" sieves, in which part of the recycled Li solution and the pure LiCl solution obtained at the end of the previous process were partially exchanged.
    [54] Two alternatives to the initial startup phase described in detail above are somewhat economically advantageous because they limit the loss of lithium.
    [55] In the preferred case where the plant operates with three columns, two alternatives can be applied at the end of the cycle:
    [56] The cleaning is continued through a line of three columns (Li solution is recovered for recycling on “new” beads at the beginning of the next process) and the line is to be used to start the next process. Drying two charges of the exchanged beads,
    [57] Alternatively, the exchange is continued on a three column line with the recovery of the Li rich solution 5 generated to achieve Li 96% exchangeability in the beads of the final column of the carousel.
    [58] It will be advantageous if these solutions are used as the initial starting solution.
    [59] The temperature of the solution of the lithium compound is preferably 80 to 120 ° C, in particular 110 to 120 ° C. It is contemplated that higher temperatures may be advantageously used by applying pressure to the system at pressures above the vapor pressure of the exchange solution at that temperature.
    [60] The lithium concentration of the solution, limited by the solubility of the salt, is chosen as high as possible to reduce the costs associated with reprocessing. Preference is given to using lithium solutions having a concentration of 1 to 10 M, preferably 3 to 6 M.
    [61] It is advantageous to add a purification step by crystallization of LiCl bleed to the process: this step allows for the selective removal of most of the NaCl and KCl residues present in the bleed, instead of the stream "e" during the next exchange run. Allow NaCl and KCl residues to be recycled (prior to release). Thus, independent loops for sodium and potassium extraction are generated.
    [62] In addition, the carousel is thermally recovered faster and the benefits of minimizing the loss of lithium by recycling before releasing the final effluent (NaCl + KCl + trace amounts of LiCl) from the last vessel of the carousel and then charging zeolite X. Taken as a condition, the operation of the carousel can be further improved.
    [63] The zeolites produced are advantageously used as adsorbents of nitrogen present in gas mixtures, in particular in air, so that it is possible to separate nitrogen from other gases present in the gas mixture. The separation is performed by passing the gas mixture through one or more adsorption zones containing the zeolites thus prepared.
    [64] The following examples provide a better understanding of the present invention.
    [65] Example 1 (comparative example)
    [66] a. Preparation of Na, K, M, LSX Beads with Diameter 1.6-2.5 mm
    [67] 1,000 liters of industrial soft water is placed in a vessel with a propeller stirrer. Si / Al atomic ratio 1, 77% of exchangeable cationic sites filled with sodium, 23% filled with potassium, volume 0.262 cm 3 / g (measured by toluene adsorption at 25 ° C. under a relative pressure of 0.5) 200 kg of zeolite LSX powder (amount considered to be anhydride) with micropores and Dubinin volume of 0.325 cm 3 / g is added with stirring (100 revolutions / minute, ambient speed = 3.5 m / s). Industrial Hittometal Chloride Solution sold by Rhodia under the trademark LADI (16.6 wt.% La 2 O 3 and 7.2 wt.% Pr 2 O 3 , concentrated lanthanum and praseodymium chloride, water and other rare earth metals (Ce, 45 kg of an aqueous solution comprising a residue consisting mainly of chloride of Nd) is then introduced over approximately 10 minutes or more. Stirring is reduced to 20 revolutions / minute and the reactor is maintained under these conditions for about 1 hour so that at the end of this time the mixture finally becomes homogeneous and the powder thus obtained is filtered, washed and dried.
    [68] The powder is subsequently agglomerated with clay binders at a level of 17% by weight (in terms of total flocculated material). The product is molded into beads of diameter 1.6-2.5 mm. These beads are dried at 80 ° C. and then activated at 580 ° C. under dry air free of carbon dioxide according to the LTC (crossed bed) technique (eg disclosed in EP 421,875).
    [69] The analysis of aggregated and exchanged zeolites, expressed as a percentage of the initial zeolite LSX exchange capacity, is thus as follows.
    [70] Hito metal equivalent 14%
    [71] Sodium equivalent 69%
    [72] Potassium Equivalent 17%
    [73] b. Lithium exchange according to the method of the present invention (the target degree of lithium exchange is 96%)
    [74] b-1. The carousel consists of three cylindrical columns H (head column), M (middle column) and T (tail column), the column has a cross section of 0.695 m 2, the bed height is 6 m, the top distributor and the bottom of the column With a support grid with sieves suitable for the specific size of beads, each column is sifted with 2,700 kg of beads prepared in step a.
    [75] The initial start-up of the carousel consists of filtering the lithium chloride solution over three columns of the carousel in the downward direction. The amount of Li filtered is approximately 4.7 E 0 (first, 1.7 E 0 for an aqueous LiCl solution containing about 7 g / l Na and 1.5 g / l K, 3 E 0 for a pure LiCl solution). LiCl solutions having concentrations of 1 M and 4 M, respectively, were adjusted to 115 ° C. before being fed continuously to a three column line. Filtration is carried out at a rate of 15 cm / min.
    [76] At the end of the filtration, the head column H, which has 94% exchange rate for the lithium of the beads, is cleaned, then discharged and freshly charged with new beads. This bed of beads is then placed in the tail of the exchange line. As a result, the normal action (filtration of LiCl solution with concentration equal to 1.1 E 0 ) begins according to the following cycle:
    [77] 1) Delivery of 2,700 kg (anhydride equivalents) of fresh beads into the free column of carousel substantially positioned at the tail position of the carousel, as described above.
    [78] 2) filtration over a tail column of recycled LiCl solution from the previous cycle; The solution contains about 0.3 E 0 Li but is rich in Na + K and corresponds to the final liquid amount (fixed) of the column forced out of the carousel for the entire cycle. This step allows, on the one hand, to fix approximately 50% of the Li present in the recycled solution to the new beads, and on the other hand to preheat the new column to facilitate subsequent exchange with Li ("final recycling"). Let's do it.
    [79] During this step (essentially water soaking) the effluent 2 resulting from the carousel is sent directly to the effluent treatment plant.
    [80] 3) Filtration on a 10 m3 head column of pure LiCl solution with a concentration of 1.4 M at 115 ° C (1.1 E 0 equivalent of Li, ie "e" = 0.1 E 0 )
    [81] Filtration is carried out over the entire length of the exchange line at a rate of 15 cm / min; It is deficient in Li (about 0.15 E 0 ), rich in Na + K and recovered (10 m 3) effluent is also directly connected to the effluent treatment plant 3.
    [82] The choice of filtration rate depends on the flow control conditions:
    [83] Just as plug flow is necessary to ensure a systematic organization of the head in the filtration column, a minimum pressure drop is necessary to avoid excessively large preferred flow rates. Considering the size of the beads to be used, the optimum filtration rate is determined to be 15 cm / min.
    [84] Although Li concentration is suitable for the exchange, dilution of the LiCl solution was chosen to increase the volume of the solution because it is advantageous that the contact time is dynamic.
    [85] 4) Cleaning of the head column where most of the carousel is completely replaced.
    [86] This step consists in "forced" the liquid content of the head column by filtration of 4.5 m 3 tap water at 15 cm / min over the entire length of the carousel (ie, the true step of Li filtration). The solution recovered at the outlet of the exchange line will be recovered to a designated vessel and recycled in the next cycle with filtration (finishing recycle 2) on a new column of new beads.
    [87] Further cleaning is mainly carried out by filtration with tap water of 0.5 m 3 on the head column to ensure minimization of the residual amount of chloride on the lithium exchange beads.
    [88] 5) Separation of the head column and transfer to the drying zone of the charge (4).
    [89] The cycle then ends and the carousel returns to normal with a new charge of new beads.
    [90] In summary, the manufacturing cycle is shown in the accompanying drawings.
    [91] With the passage of the cycle, the level of exchange for the removed head column for lithium decreases, resulting in a tendency to fall below the target (96%) (91%-92%):
    [92] -94% after starting
    [93] 93.5% after first cycle
    [94] -92% after the second cycle
    [95] 91.8% after the third cycle
    [96] When carried out under stable conditions, the maximum level of exchange of lithium obtained is 92% or less and the production is 87% for fixed lithium.
    [97] b-2. The exchange of lithium, except that in normal operation the filtration on the head column is carried out at 115 ° C. with a 1.4 M pure solution of LiCl (Li, ie 1.3 E 0 equivalents of 0.3 E 0 , instead of 0.1 E 0 ). And under the same performance conditions, and is carried out on the beads prepared in step a of the same carousel as described in b-1.
    [98] After start-up, the beads in the carousel's head column show an exchange rate equal to 98% for lithium, but as a result of the next cycle (still running at 1.3 E 0 ), the exchange rate for lithium decreases with each cycle. It shows a tendency to have a value of 92 to 93% (distant from this target 96%).
    [99] -98% after starting
    [100] 98% after the first cycle (forced start effect)
    [101] 95% after the second cycle
    [102] 94.2% after the third cycle
    [103] 93.5% after the fourth cycle
    [104] 92.5% after the fifth cycle.
    [105] When carried out under stable conditions, the maximum exchange level for lithium obtained is on the order of 92.5% and the yield is only 74%.
    [106] Example 2
    [107] Example 1 The beads prepared in a are placed in a carousel as defined in Example 1. b-1, wherein lithium exchange is performed according to the method defined above:
    [108] 1-initial start-up of the carousel, the action of which consists of installing a system of three columns, at the Li exchange level, such that the method runs from the inlet of fresh charge to the carousel,
    [109] 2-normal operation (following the same method as described in Example 1, leading to stable results throughout each cycle),
    [110] 3-End of cycle.
    [111] The initial start-up (1-) consists of filtering the lithium chloride (1) solution on three columns of bead-filled carousel, where the amount of Li filtered is about 4 E 0 and the LiCl solution at a concentration of 4 M is 3 Up to 115 ° C. before feeding on the column. Filtration is carried out at a rate of 12 cm / minute.
    [112] Example 1 In comparison with the methods for the lithium exchange of b-1 and b-2,
    [113] The action is carried out with LiCl solution 1 having a concentration of 4 M:
    [114] 1-has the advantage of optimum propulsion for lithium exchange,
    [115] 2-On the one hand, the volume of effluent to be treated is reduced, and on the other hand, the volume of solution to be recovered is reduced, which is a significant advantage (reduced transportation costs) in cases where the solution to be recovered must be transported.
    [116] Filtration speed is reduced to 12 cm / min, not excessively reducing dynamic contact time (optimal contact time / flow rate, concentration of solution to be fixed).
    [117] At the end of the filtration, the head column with a degree of exchange of 96% of the zone with respect to the lithium of the beads is washed, then discharged and freshly charged with new beads. This bed of beads is then placed in the tail of the exchange line. After that, normal action begins.
    [118] Normal action according to 2-) follows the cycle:
    [119] 1) Transfer of 2,700 kg (anhydride equivalents) of fresh beads into the free column of the carousel virtually located at the tail location of the carousel.
    [120] 2) filtration over a tail column of recycled LiCl solution from the previous cycle; The solution contains about 0.3 E 0 Li, but is rich in Na + K, corresponding to the final amount of liquid in the column forced out of the carousel during the previous cycle. This step firstly secures approximately 50% of the Li present in the recycled solution to the new beads, and secondly preheats the new column to facilitate subsequent exchange with Li (final recycling (2)). do.
    [121] During this step (essentially water soaking) the effluent 2 resulting from the carousel is sent directly to the effluent treatment plant.
    [122] 3) Filtration on a 6.6 m 3 head column of pure LiCl solution with a concentration of 4 M at 115 ° C. (Li 2.2 E 0 equivalents, ie “e” = 1.2 E 0 ):
    [123] In the first step, 4.5 m3 (approximate solution content of the head column) with an Li-rich (about 1.05 E 0 ) and low Na + K solution (5) is extracted from the bottom of the head column. This solution (5), which can be effectively and easily recovered, has the following average characteristics:
    [124] Li concentration of 19 to 20 g / l
    [125] Li / Na molar ratio of 6 to 8
    [126] Li / K molar ratio of 50 to 60
    [127] In the second step, the filtration is carried out at the same rate of 12 cm / min over the entire length of the exchange line, with less Li (about 0.15 0 , corresponding to the result of the recycle filtration performed on the new column at the beginning of the cycle). The recovered effluent (2.1 m 3) 3 enriched in Na + K is sent directly to the effluent treatment plant.
    [128] 4) Cleaning of the head column exchanged to 96% level for Li at this stage of the cycle.
    [129] This step consists in draining the liquid content of the head column (or hold-up) by filtration of 4.5 m 3 tap water at 12 cm / min over the entire length of the carousel (ie, the true step of Li filtration). . The solution recovered at the outlet of the exchange line will be stored in the designated vessel and recycled in the next cycle with filtration (finishing recycle 2) on a new column of "new" beads.
    [130] Further cleaning is mainly carried out by filtration with tap water of 0.5 m 3 on the head column to ensure minimization of the residual amount of chloride in the lithium exchange beads.
    [131] 5) Separation of the head column 4 and transfer to the drying zone of the filling.
    [132] The cycle then ends and the carousel returns to normal with a new charge of new beads.
    [133] In summary, a manufacturing cycle is shown in the accompanying drawings.
    [134] When carried out under stable conditions, the maximum level of exchange for the lithium obtained was 96%, the yield was 45%, and the stream could easily be recovered at the outlet of the carousel.
    [135] Example 3
    [136] Prior to flocculation according to the method described in detail in Example 1.a, the zeolite NaK LSX of Example 1.a is suspended in an aqueous solution of a salt of the histometal and Na and the zeolite NaK LSX in water to form a Co-exchange of sodium ions removes the cationic sites of zeolites filled with potassium ions to 10% or less (degree of exchange for the sum of Na + K). An agglomerated zeolite is obtained in which the Na level is at least 90% of the level of Na + K in the starting zeolite and the degree of exchange for trivalent rare earth metal cations is about 14%.
    [137] The beads thus obtained are placed in a carousel as defined in Example 1. b-1, wherein lithium exchange of the zeolite of the beads is carried out according to the method defined in Example 1.
    [138] Li filtration is performed according to the method described in Example 2 with the following changes.
    [139] During the initial startup phase, the amount of Li filtered is about 4 E 0 . The 5 M concentration of LiCl solution is brought to 115 ° C. before being fed to a three column line, and filtration is carried out at a rate of 12 cm / min.
    [140] Using a LiCl solution having a concentration of 5 M, and beads having a K content less than those of Example 1.a, the precipitation limit of the LiCl / NaCl / KCl solution in the column of the carousel is lowered.
    [141] Increasing the LiCl concentration to 5 M enables the following points compared to the method of Example 2:
    [142] 1-has the advantage of optimum propulsion for lithium exchange,
    [143] 2-The advantage is to reduce the volume of effluent to be treated first, and to reduce the volume of solution to be effectively recovered second.
    [144] The filtration rate is maintained at 12 cm / min, without further reducing the dynamic contact time. The case of filling beads of smaller diameter is advantageous.
    [145] At the end of the filtration, the head column which has been 96% exchanged for Li is washed, then discharged and replaced with fresh fill of fresh sieve. This bed of beads is then placed in the tail of the exchange line. After that time, following the next cycle, normal action begins:
    [146] 1) Delivery of 2,700 kg (anhydride equivalents) of new beads of Na, εK, M, LSX into the free column of the carousel which is virtually located at the tail position of the carousel .
    [147] 2) filtration over a tail column of recycled LiCl solution from the previous cycle; The solution contains about 0.3 0 Li, but rich in Na, corresponding to the final amount of liquid in the column forced out of the carousel during the previous cycle.
    [148] This step firstly secures approximately 50% of the Li present in the recycled solution to the new beads, and secondly preheats the new column to facilitate subsequent exchange with Li (final recycling (2)). do.
    [149] The effluent from the carousel during this step (essentially water soaking) is sent directly to the effluent treatment plant 3.
    [150] 3) Filtration on 5.3 m 3 head column of pure LiCl solution with a concentration of 5 M at 115 ° C. (Li 2.2 E 0 equivalent, ie “e” = 1.2 E 0 ):
    [151] In the first step, 3.6 m3 (approximate solution content of the head column) with an aqueous solution rich in Li (about 1.05 E 0 ) and low in Na + εK are extracted at the bottom of the head column. This solution, which can be effectively and easily recovered, has the following average characteristics:
    [152] Li concentration of 23 to 25 g / l
    [153] 4.5 Li / Na molar ratio
    [154] -About 160 Li / K molar ratio
    [155] In the second step, filtration is carried out at the same rate of 12 cm / min over the entire length of the exchange line, with less Li (about 0.15 0 ; this is the result of recycle filtration performed on a new column at the beginning of the cycle), The recovered effluent (1.7 m 3) rich in Na + K is sent directly to the effluent treatment plant 3.
    [156] 4) Cleaning of the head column exchanged to 96% level for Li in this step of the cycle.
    [157] This step consists in draining the liquid content of the head column by filtration of 4.5 m 3 tap water at 12 cm / min over the entire length of the carousel (which in fact corresponds to the true step of Li filtration). The solution recovered at the outlet of the exchange line will be recovered to the designated vessel and recycled in the next cycle with filtration (finishing recycle 2) on a new column of "new" beads.
    [158] Further cleaning is mainly carried out by filtration with tap water of 0.5 m 3 on the head column to ensure minimization of the residual amount of chloride in the lithium exchange beads.
    [159] 5) Separation of the head column and transfer to the drying area of the filling.
    [160] The cycle then ends and the carousel is returned to its new fill with new beads.
    [161] Here again two alternatives can be used at the end of the cycle:
    [162] The cleaning is continued through a line of three columns (Li solution is recovered for recycling on “new” beads at the beginning of the next process) and the line is pre-exchanged, which will be used to start the next process. Drying the filling of the two beads,
    [163] Or continue the exchange on a three column line with the recovery of Li rich solution generated in order to achieve a 96% exchange rate of Li in the zeolite of the beads filling the final column of the carousel. These solutions can be used as starting solutions in the following process.
    [164] In summary, a manufacturing cycle is shown in the accompanying drawings.
    [165] The method provides the following:
    [166] The -Li exchange level is slightly higher than the Li exchange degree obtained in Example 2, and on average exceeds 96% because of increased Li exchangeability in Na-εK LSX substrates compared to Na-K LSX substrates.
    [167] Secondly, due to the low K content, the effective recovery of the Li solution collected at the bottom of the head column is increased so that the solution is fully recovered after removing Na from the optional crystallization unit of the replenishment. It became.
    [168] Example 4
    [169] Beads agglomerated according to the method described in Example 1.a are lithium exchanged according to the method of Example 3 with the following changes:
    [170] The phase extracted from the head column (bleed) in n-1 cycles (3.6 m 3) is treated with the following matters:
    [171] Lithium concentration of -23/25 g / l
    [172] 4.5 Li / Na molar ratio
    [173] -About 160 Li / K molar ratio
    [174] The treatment is by the following steps:
    [175] 1. Concentration suitable for the preparation of concentrates having a LiCl content of about 400 g / l under vacuum at a temperature on the order of 70 ° C.
    [176] 2. Cool one stage NaCl-rich stream to about 25 ° C using a suitable heat exchanger.
    [177] 3. Filtration of a two-stage LiCl-rich stream in a conventional manner to minimize the loss of lithium chloride.
    [178] 4. Dilute with water so that the concentration of lithium (relative to LiCl) is 5 M.
    [179] This results in about 2,400 L of a 5 M concentration of LiCl solution comprising less than 2 g / l NaCl and less than 3 g / l KCl.
    [180] N cycles
    [181] 2.4 m 3 of a 5 M LiCl solution treated as described above,
    [182] Filtration of 2.9 m3 of pure 5 M LiCl solution
    [183] The production cycle then proceeds according to the method described in Example 2, and considering the inherent losses in the method for the concentration / purification of lithium bleed described above, the lithium production is 85% as in Examples 1-3. Exceeded.
    [184] Example 5
    [185] Before flocculation according to the method described in detail in Example 1.a, the zeolite NaK LSX of Example 1.a is suspended in an aqueous solution of a salt of Na and the zeolite NaK LSX in water to form a cationic site of zeolite filled with potassium. Exchange with sodium ions to bring the level up to 8% (which is the exchange degree for the sum of Na + K). Agglomerated zeolites are obtained in which Na levels are at least 92% of the levels of Na + K in the starting zeolite.
    [186] The following exchange of lithium is performed on the beads thus prepared, and secondly, lithium exchange in beads of NaK LSK zeolite, which has not been exchanged of sodium ions, is performed.
    [187] Beads were placed in the carousel as defined in Example 1. b-1. In the apparatus, lithium exchange of the zeolite of the beads is carried out according to the method defined in Example 3.
    [188] At the end of filtration (4E 0 equivalents of Li), more than 96% of the exchanged head column for Li is washed, then discharged and replaced with fresh fill of new sieve. This bed of beads is then placed in the tail of the exchange line. After that time, following the next cycle, normal action begins:
    [189] 1) Delivery of 2,700 kg (anhydride equivalents) of new beads of Na, εK, LSX into the free column of the carousel which is virtually located at the tail position of the carousel.
    [190] 2) filtration over tail columns of recycled LiCl solution from all cycles; The solution is one containing about 0.3 Li 0, Na is rich, corresponding to a fixed final liquid volume of the column was removed binary force on the car-go for the entire cycle.
    [191] This step not only fixes approximately 50% of Li present in the recycled solution to the new beads, but also makes it possible to significantly lower the residual potassium content in the starting zeolite. In addition, it is possible to preheat the new column to facilitate next exchange with Li (final recycling 2).
    [192] The effluent 3 resulting from the carousel during this step (essentially wet with a stream rich in sodium and potassium as well as water) is sent directly to the effluent treatment plant.
    [193] 3) Filtration on a 6.6 m 3 head column of a pure LiCl solution with a concentration of 5 M at 115 ° C. (Li 2.2 E 0 equivalents, ie “e” = 1.2 E 0 ):
    [194] In the first step, a solution rich in Li (about 1.05 E 0 ) and low in Na + εK 4.2 m3 (approximately fixed to the column) is extracted from the bottom of the head column. This solution, which can be effectively and easily recovered, has the following average characteristics:
    [195] Li concentration of 23 to 25 g / l
    [196] -About 5.5 Li / Na molar ratio
    [197] -About 200 Li / K molar ratio
    [198] In the second step, filtration is carried out at the same rate of 12 cm / min over the entire length of the exchange line, with less Li (about 0.15 0 ; this is the result of recycle filtration performed on a new column at the beginning of the cycle), The Na-rich recovered effluent (2.4 m 3) is sent directly to the effluent treatment plant 3.
    [199] 4) Cleaning of the head column exchanged to 96% level for Li in this step of the cycle.
    [200] This step consists in draining the liquid content of the head column by filtration of 4.5 m 3 tap water at 12 cm / min over the entire length of the carousel (which in fact corresponds to the true step of Li filtration). The solution recovered at the outlet of the exchange line will be recovered to the designated vessel and recycled in the next cycle with filtration (finishing recycle 2) on a new column of "new" beads.
    [201] Further cleaning is mainly carried out by filtration with tap water of 0.5 m 3 on the head column to ensure minimization of the residual amount of chloride in the lithium exchange beads.
    [202] 5) Separation of the head column and transfer to the drying area of the filling.
    [203] The cycle then ends and the carousel returns to normal with a new charge of new beads.
    [204] After 8 cycles, the new column is replaced with zeolite Na K LSX beads with no sodium pre-exchanged.
    [205] The change from Na εK LSX beads (NaK LSX beads pre- exchanged with sodium) to NaK LSK beads (not pre- exchanged with sodium) does not alter the quality of the 4.2 m 3 stream extracted from the head column, especially the content of potassium ( The potassium content of the starting zeolite remained below 0.5 g / l, despite a significant increase in the content of the starting zeolites.
    [206] Therefore, by design pre-exchange of sodium (if not carried out interchangeably with divalent and / or trivalent ions) is unnecessary for production with a K content of less than 1 g / l in the stream. It is sufficient to initiate the filtration cycle with beads pre-exchanged with sodium. The final recycling step is then carried out with a stream containing Li / Na and Na / K ratios for the selective extraction of potassium present in the zeolites of the tail column. The final product (K content of bleed) is thus equivalent to that obtained with zeolites pre-exchanged with sodium.
    [207] According to an optional determination step described in Example 4, the phase extracted from the head column (bleed) in n-1 cycles (4.2 m 3) is as follows:
    [208] Lithium concentration of -24 g / l
    [209] -About 5.5 Li / Na molar ratio
    [210] When treated with a Li / K molar ratio of about 200, about 2,600 L of a 5 M concentration of LiCl solution containing less than 2 g / l NaCl and less than 2 g / l KCl is obtained.
    [211] The treated stream of 2.6 m 3 of 5 M LiCl solution is filtered in n cycles before being supplemented with 4 m 3 of pure 5 M LiCl solution.
    [212] The production cycle is then carried out according to the method described in Example 2, with greater than 85% Li production taking into account the losses inherent in the method for the concentration / purification of lithium bleed described above.
    [213] The method makes it possible to achieve a high level of lithium exchange with significantly improved lithium yield over the prior art methods.
    权利要求:
    Claims (9)
    [1" claim-type="Currently amended] The atomic ratio of Si / Al is 1.5 or less, preferably 0.9 to 1.1, and exchangeable cations are represented by equivalent weight.
    About 50 to about 99% and preferably at least 96% of lithium ions,
    Trivalent ions selected from aluminum, scandium, gallium, iron (III), chromium (III), indium, yttrium, lanthanide or rare earth metals alone or in mixtures, and / or calcium, strontium, zinc, copper, chromium (II) About 4 to about 50% of a divalent ion selected from iron (II), manganese, nickel or cobalt alone or in a mixture,
    0 to about 15% residual ions selected from sodium, potassium, ammonium or hydronium alone or in mixtures
    A method for producing an X-type zeolite aggregated with a binder, wherein the exchangeable cation is sodium, potassium, ammonium and / or hydronium cations and / or divalent and / or trivalent cations. A portion of the exchangeable cation of is exchanged for lithium,
    The exchange transports the zeolite distributed in the vessel through the vessels (ie, carousel) arranged in series, in the form of two or more, preferably three or more static beds arranged in series in a mutually changeable manner. Contact with the lithium compound solution (1), the sequence of the vessels being controlled periodically at a given time interval, and the inlet of the fresh solution in each case in the first vessel where the zeolite exchanged to the maximum is found. Move to the next container in the series; When lithium is exchanged in the first vessel by the desired amount in the zeolite, the first vessel is removed from the series of carousels, the zeolite present in it is washed, removed from the solution of the lithium compound, and released (4) Consisting of exchanging with a fresh zeolite charge which is to be exchanged at random,
    The bleed 5 is separated from the effluent generated by the carousel and discharged from the stream corresponding to the excess of lithium used and
    The first stream 5 corresponding to filtration "e" at the outlet of the head column of the carousel
    Subsequent stream (3) corresponding to the filtration "E 0 " at the outlet of the carousel.
    (“E 0 ” is the stoichiometric equivalent of exchangeable lithium in a sieve and “e” is the excess required to obtain the desired degree of exchange for lithium, preferably greater than 96%) in the carousel Discharged
    A method for producing an X-type zeolite, characterized in that.
    [2" claim-type="Currently amended] The process of claim 1 wherein the temperature of the solution of the lithium compound is 80 to 120 ° C., preferably 110 to 120 ° C., or 120 ° C., if the pressure is applied to the system at a temperature under consideration, preferably above the vapor pressure of the exchange solution. Characterized in that it exceeds.
    [3" claim-type="Currently amended] Method according to claim 1 or 2, characterized in that the concentration of the solution of the lithium compound is 1 to 10 M, preferably 3 to 6 M.
    [4" claim-type="Currently amended] The process according to any one of claims 1 to 3, wherein the degree of exchange with respect to the potassium of the zeolite prior to lithium exchange is at most 15%, preferably at most 10% of all exchangeable sites.
    [5" claim-type="Currently amended] 5. The method according to claim 1, wherein very large amounts (even all) of the exchangeable cations of the starting zeolite, before the lithium exchange, before and / or after the agglomeration step of the zeolite, Preferably comprising converting to sodium or ammonium ion form.
    [6" claim-type="Currently amended] The process according to any one of claims 1 to 5, comprising the step of purifying by crystallization of LiCl bleed.
    [7" claim-type="Currently amended] The method of claim 1, wherein the final effluent (NaCl + KCl + trace amounts of LiCl) is recycled to the last vessel of the carousel.
    [8" claim-type="Currently amended] 8. A column system according to any one of the preceding claims, wherein the initial starting step is to install a column system at the Li exchange level, preferably by filtering the lithium chloride solution 1 on a column of carousel filled with starting zeolite.
    In the first and second places of the exchange line, install two pre-exchanged columns obtained at the end of the previous compilation and install columns of "virgin" beads in the tail position,
    Starting with three columns of "new" sieves, with partial replacement of the pure LiCl solution with the recycled Li solution obtained at the end of the previous process
    Characterized in that the starting zeolite is distributed in three static beds.
    [9" claim-type="Currently amended] The method of claim 8, wherein at the end of the cycle,
    The washing is continued through a line of three columns (Li solution is recovered for recycling on "new" beads at the beginning of the next process) and two charges of pre-changed beads to be used to start the next process Dry it,
    Or, exchange on a three column line with the recovery of the generated Li rich solution 5 which is advantageously used as the initial starting solution, in order to achieve 96% exchangeability of Li in the beads of the final column of the carousel. This will continue
    Characterized by the above.
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    同族专利:
    公开号 | 公开日
    HK1046265B|2009-12-24|
    JP2002087813A|2002-03-27|
    IL144005A|2005-03-20|
    HK1046265A1|2009-12-24|
    BR0102774A|2002-02-19|
    CN100486893C|2009-05-13|
    DE60102419T2|2005-03-10|
    CA2352412A1|2002-01-07|
    AR029568A1|2003-07-02|
    IL144005D0|2002-04-21|
    US20020031472A1|2002-03-14|
    EP1170254B1|2004-03-24|
    AT262489T|2004-04-15|
    SG99912A1|2003-11-27|
    KR100776550B1|2007-11-16|
    DE60102419D1|2004-04-29|
    TWI228103B|2005-02-21|
    FR2811313A1|2002-01-11|
    JP4953181B2|2012-06-13|
    US6649556B2|2003-11-18|
    CN1344677A|2002-04-17|
    FR2811313B1|2002-08-30|
    EP1170254A1|2002-01-09|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-07-07|Priority to FRFR00/08906
    2000-07-07|Priority to FR0008906A
    2001-07-06|Application filed by 쇼송 빠뜨리시아, 세카 에스. 에이.
    2002-01-17|Publication of KR20020005495A
    2007-11-16|Application granted
    2007-11-16|Publication of KR100776550B1
    优先权:
    申请号 | 申请日 | 专利标题
    FRFR00/08906|2000-07-07|
    FR0008906A|FR2811313B1|2000-07-07|2000-07-07|Process for the preparation of zeolites x and lsx agglomerated and exchanged with lithium|
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