Patent Application
20180015426
The invention relates to the field of filtering structures made of an inorganic material which are intended for the filtration of liquids, in particular the structures coated with a membrane in order to separate particles or molecules from a liquid, more particularly from water.
Filters which use ceramic or nonceramic membranes to carry out the filtration of various fluids, in particular polluted water, have been known for a long time. These filters can operate according to the principle of frontal filtration, this technique involving the passage of the fluid to be treated through a filtering media perpendicularly to its surface. This technique is limited by the accumulation of particles and the formation of a cake at the surface of the filtering media. This technique is thus more particularly suitable for the filtration of liquids not comprising high loads of pollutants (that is to say, the liquid or solid particles in suspension).
According to another technique to which the present invention also relates, use is made of tangential filtration which, in contrast, makes it possible to limit the accumulation of particles by virtue of the longitudinal circulation of the fluid at the surface of the membrane. The particles remain in the circulating stream, while the liquid can pass through the membrane under the effect of the pressure. This technique provides stability of the performance and of the level of filtration.
The strong points of tangential filtration are thus its ease of use, its reliability, by virtue of the use of organic and/or inorganic membranes, the porosity of which is suitable for carrying out said filtration, and its continuous operation. Tangential filtration requires little or no adjuvant and provides two separate fluids which may both be of economic value: the concentrate (also known as retentate) and the filtrate (also known as permeate); it is regarded as a clean process which is environmentally friendly. Tangential filtration techniques are used in particular for microfiltration or ultrafiltration. The tangential configuration generally requires the use of at least two pumps, one a pressurization (or booster) pump and the other a recirculation pump. The recirculation pump often exhibits the disadvantage of a sizable energy consumption. The use of filtering devices guaranteeing high flow rates of the filtrate would make it possible to limit the energy consumption.
The present invention is thus suitable just as much for tangential filters as for frontal filtration filters.
Numerous filter structures operated according to the principles of tangential filtration or of frontal filtration are thus known from the current art. They comprise or are formed from tubular or parallelepipedal supports made of a porous inorganic material formed of walls delimiting longitudinal channels parallel to the axis of said supports.
In the case of tangential filters, the filtrate passes through the walls and is then discharged at the peripheral external surface of the porous support. These filters are more particularly suitable for filtering liquids having high loads of particles.
In the case of the frontal filters, the longitudinal channels are normally blocked at one end, for example alternately, so as to form inlet channels and outlet channels separated by the walls of the channels, the inlet and/or outlet channels being coated with a filtering membrane through which all the liquid passes, the particles being retained by the membrane.
The surface of said channels is generally normally covered with a membrane, preferably made of a porous inorganic material, known as membrane, membrane layer or separating membrane layer in the present description, the nature and the morphology of which are suitable for halting the molecules or the particles, the size of which is close to or greater than the median diameter of the pores of said membrane, when the filtrate spreads through the porosity of the porous support under the pressure of the fluid passing through the filter. The membrane is conventionally deposited on the internal surface of the channels by a process of coating a slip of the porous inorganic material, followed by a consolidation heat treatment, in particular a drying and generally a sintering of the ceramic membranes.
Numerous publications indicate different configurations of the traversing channels which are targeted at obtaining a filter exhibiting the optimum properties for the application and in particular:
The studies carried out by the applicant company have shown, according to another complementary approach, that, within such filtering structures, it is of use to adjust the chemical composition of the separating membrane, in order to further improve the filtration performance of the structure, indeed even the lifetime of the filter. Such an aim is achieved in particular by the improvement to the resistance to abrasion of the membrane of the filter according to the invention, which can for this reason operate effectively over a substantially greater lifetime.
Numerous documents of the art describe different possible compositions for the ceramic membrane made of porous inorganic material without, however, establishing a causal relationship between the composition of the material constituting the membrane and the performance of the filter. According to one implementation, the application FR 2 549 736 proposes to increase the flow of filtered liquid by specifying the size of the particles forming the filtering layer, with respect to those forming the support. However, the layers made of alumina disclosed exhibit a flow regarded as weak from the viewpoint of the present invention.
Other publications, for example the patent application EP 0 219 383 A1, mention the use of silicon carbide and nitride as constituent material of the membrane. According to Example 2 of this publication, a filtering body, including the membrane layer formed of SiC particles, is directly calcined under nitrogen at a temperature of 1050° C. The resistance to abrasion of the membrane thus obtained has, however, appeared too low to make it possible to obtain filters having a prolonged lifetime.
The patent application WO 03/024892 describes a method of preparation of a support or of a membrane produced from a mixture of coarse α-SiC particles, of a metalic silicon powder and of a carbon precursor which are intended to form, between the coarse grains, a bonding phase of fine β-SiC particles. The bonding phase is finally subsequently converted, according to this teaching, into α-SiC by firing at a very high temperature (typically 1900 to 2300° C.)
The patent U.S. Pat. No. 7,699,903 B2 describes separating membrane layers made of silicon carbide starting from a mixture of two powders of α-SiC particles sintered together at a temperature of between 1750 and 1950° C.
The document EP 2 511 250 describes a porous support comprising SiC grains, the surface of which is covered with a nitrogen-comprising layer. This nitrogen layer is obtained by a nitridation treatment which makes it possible to control the resistivity for combustion gas decontamination. According to this publication, an attempt is made to thus obtain a filter or more exactly a support element made of SiC doped with nitrogen, the conductivity of which as a function of the temperature is controlled. It is clearly indicated in this document that said nitridation is carried out on the SiC grains constituting the porous support. The document thus does not describe the deposition of an additional layer (i.e., a separating membrane layer) on the internal surface of the channels or the external surface of the filtering element before nitridation.
Patent application EP 2 484 433 describes a particle filter for the purification of exhaust gases, the porous walls of which can comprise SiC and other particles than SiC, it being possible for these particles to be chosen from an oxide, an oxynitride or a nitride of an element of Groups 3 to 14 of the Periodic Table.
In the present description, the terms separating membranes, separating layer or separating membrane layer are used without distinction to denote such membranes which make possible filtration.
The object of the present invention is to provide a filter incorporating a filtering membrane which is resistant whatever its condition of use and the longevity of which is thus found to be improved thereby, for a filtration performance which is identical or substantially improved with respect to prior implementations.
A nitridation according to the invention of a powder of metalic silicon grains advantageously makes it possible to obtain a controlled distribution of the pore sizes and in particular a narrow distribution in pore sizes centered on a smaller median pore diameter. Such a material can thus potentially make it possible to achieve membranes of high selectivity, due to said distribution.
In particular, an optimum in terms of resistance to abrasion and of chemical resistance has been demonstrated by the studies of the applicant company, described below, by an appropriate selection of the constituent material of said composite membranes made of SiC-nitride or SiC-oxynitride obtained by the reactive sintering process according to the invention.
The invention thus relates, according to a first aspect, to a filtering structure or filter configured for the filtration of a fluid, such as a liquid, comprising or composed of a support element made of a porous ceramic material, said element exhibiting a tubular or parallelepipedal shape delimited by an external surface and comprising, in its internal portion, a set of adjacent channels, with axes parallel to one another and separated from one another by walls of said porous inorganic material, in which at least a portion of said channels are covered on their internal surface (and/or on said external wall, according to certain filter configurations) with a porous separating membrane layer. During the operation of the filter, this layer, as indicated above, comes into contact with said fluid to be filtered circulating in said channels in order to make possible the tangential or frontal filtration thereof.
In a filter according to the present invention:
According to preferred embodiments of the present invention:
In the present description, unless otherwise specified, all percentages are by weight.
As regards the porous support, the following information relating to preferred but nonlimiting embodiments of the present invention is given:
Dh=4×S/P
As indicated above, the filter according to the invention can comprise, in addition to the separating membrane layer, one or more primer layers arranged between the material constituting the support element and the material constituting the separating membrane layer. The role of this (these) “primer” layer(s) consists in facilitating the tying of the separating layer and/or in preventing the particles of the separating membrane from passing through the support, in particular during a deposition by coating.
The following information is additionally given:
The open porosity and the median pore diameter of the porous support described in the present description are determined in a known way by mercury porosimetry.
The porosity and the median pore diameter of the membrane are advantageously determined according to the invention using a scanning electron microscope. For example, sections of a wall of the support in cross section are produced, as illustrated by the appended
An example of determination of the median pore diameter or of the median size of the particles constituting the membrane layer, by way of illustration, comprises the following sequence of stages which is conventional in the field:
Within the meaning of the present description unless otherwise mentioned, the median size of the particles or the median diameter of the pores measured by microscopy respectively denotes the diameter of the particles or of pores below which 50% by number of the population occurs. On the other hand, as regards the pore diameter measured on the substrate by mercury porosimetry, the median diameter corresponds to a threshold of 50% of the population by volume.
The term “sintering” refers conventionally in the field of ceramics (that is to say, within the meaning indicated in the international standard ISO 836:2001, point 120) to a consolidation by heat treatment of a granular agglomerate. The heat treatment of the particles used as starting charge for obtaining the membrane layers according to the invention thus makes possible the joining and the growth of their contact interfaces by movement of the atoms inside and between said particles.
The sintering between the SiC grains and the metallic silicon grains according to the invention is normally essentially carried out in the liquid phase, the sintering temperature being close to, indeed even greater than, the melting point of metallic silicon.
The sintering can be carried out in the presence of a sintering additive, such as an iron oxide. The term “sintering additive” is understood to mean a compound known usually for making possible and/or accelerating the kinetics of the sintering reaction.
The median diameter d50 of the powders of particles used to produce the support or the membrane is given conventionally by a particle size distribution characterization, for example using a laser particle sizer.
The contents by weight of nitrogen and of oxygen of the membrane can be determined after melting under an inert gas, for example using an analyzer sold under the reference TC-436 by Leco Corporation.
The SiC content can also be measured according to a protocol defined according to the standard ANSI B74.15-1992-(R2007) by a difference between total carbon and free carbon, this difference corresponding to the carbon fixed in the form of silicon carbide.
The residual metallic silicon is measured according to the method known to a person skilled in the art and referenced under ANSI B74-151992 (R2000).
The presence and the percentages by weight of the different nitrogen-comprising crystalline phases in the membrane material, in particular of Si3N4 type (in the a or (3 crystallographic form) and/or of Si2ON2 type, and also of the SiC crystalline phases, can be determined by X-ray diffraction and Rietveld analysis.
A nonlimiting example which makes possible the preparation of a filter according to the invention, very obviously also nonlimiting of the processes which make it possible to obtain such a filter and of the process according to the present invention, is given below.
According to a first stage, the filtering support is obtained by extrusion of a paste through a die configured according to the geometry of the structure to be produced according to the invention. The extrusion is followed by a drying and by a firing in order to sinter the inorganic material constituting the support and to obtain the characteristics of porosity and of mechanical strength necessary for the application.
For example, where a support made of SiC is concerned, it can in particular be obtained according to the following manufacturing stages:
The filtering support is subsequently coated according to the invention with a membrane (or separating membrane layer). One or more layers can be deposited in order to form a membrane according to various techniques known to the person skilled in the art: techniques for deposition starting from suspensions or slips, chemical vapor deposition (CVD) techniques or thermal spraying techniques, for example plasma spraying.
Preferably, the membrane layers are deposited by coating starting from slips or suspensions. A first layer (known as primer layer) is preferably deposited in contact with the porous material constituting the substrate, acting as tie layer. A nonlimiting example of an inorganic primer formulation comprises from 30% to 50% by weight of SiC powder(s) with a median diameter of 2 to 20 microns and 1 to 10% by weight of a metallic silicon powder, typically with a median diameter of between 1 and 10 microns, the remainder being of demineralized water (apart from the optional organic additives).
Typically, a primer formulation comprises, by weight, from 25 to 35% of an SiC powder with a median diameter of 7 to 15 microns, from 10 to 20% of an SiC powder with a median diameter of 3 to 6 microns and from 5 to 15% of a silicon powder with a median diameter of 1 to 5 microns, the remainder at 100% being contributed by demineralized water (apart from the organic additives or additions).
Although preferably present, in some filter configurations this primer layer may be absent without departing from the scope of the invention.
A second layer of finer porosity is subsequently deposited on the primer layer (or directly on the support), which constitutes the membrane or separating membrane layer proper. The porosity of the latter layer is appropriate for conferring, on the filtering element, its final filtration properties.
In order to control the rheology of the slips and to observe a suitable viscosity (typically of between 0.01 and 1.5 Pa·s, preferably 0.1 and 0.8 Pa·s, under a shear gradient of 1 s−1 measured at 22° C. according to the standard DIN C 33-53019), thickening agents (according to proportions typically between 0.02 and 2% of the weight of water), bonding agents (typically between 0.5 and 20% of the weight of SiC powder) and dispersing agents (between 0.01 and 1% of the weight of SiC powder) can be added. The thickening agents are preferably cellulose derivatives, the bonding agents are preferably PVAs or acrylic derivatives and the dispersing agents are preferably of the ammonium polymethacrylate type.
Organic additions, expressed by weight of the slip, in particular Dolapix A88 as deflocculating agent, for example according to a proportion of 0.01 to 0.5%, Tylose, for example of MH4000P type, as thickener according to a proportion of 0.01 to 1%, PVA as adhesion agent in a proportion of 0.1 to 2%, expressed by dry weight, monoethylene glycol as plasticizer and 95 vol % ethanol as reducer of surface tension are more particularly appropriate.
These coating operations typically make it possible to obtain a primer layer with a thickness of approximately 30 to 40 micrometers after drying. During the second coating stage, a separating membrane layer with a thickness, for example, of approximately 30-40 μm is obtained after drying, this thickness range being, of course, in no way limiting.
The specific stages of a process according to the invention for the deposition of the separating membrane layer according to the invention on the support, optionally above the primer layer described above, are described below.
According to a first embodiment, a slip is prepared as indicated above from a powder of silicon carbide particles and from a metallic silicon powder, in a ratio by weight between the two inorganic powders (wSi/wSiC) of between 0.03 and 0.30 and preferably between 0.05 and 0.15 and in the presence of the amount of water which preferably makes it possible to observe the conditions of rheology and of viscosity which are described above, and also in the presence of the organic agents necessary, preferably, so as to obtain a slip having a pH of less than or equal to 9.
The slip is subsequently applied to the support element, under conditions and by means appropriate for making possible the formation of a thin layer on the internal part of the channels of said filter, such as in particular described above.
After application of this layer, the support is first dried at ambient temperature, typically for at least 10 minutes, and then heated at 60° C. for at least 12 hours. Finally, a porous separating membrane layer at the surface of the channels of the support is obtained by sintering in a furnace. The firing temperature is typically at least 1200° C. and is preferably less than 1600° C., in order to make possible the formation of the nitrides, during the reactive sintering between the SiC grains, the metallic silicon and the nitrogen present in the atmosphere of the sintering. The sintering temperature is preferably between 1300° C. and 1500° C., preferably between 1350° C. and 1480° C. and generally above the melting point of the metallic silicon in the initial mixture, at ambient pressure. The sintering temperature of the separating membrane layer is normally lower than the sintering temperature of the support.
As indicated above, the firing is carried out under a reducing atmosphere containing or based on nitrogen, in particular in the form of gaseous nitrogen (N2) or in the form of ammonia. The firing time is prolonged until there is obtained, in the end, a content of nitrogen present within the separating membrane layer according to the present invention. The firing can be continued by a heat treatment under a reducing atmosphere containing a mixture of nitrogen and hydrogen, for example, by volume, 5% of hydrogen H2 per 95% of nitrogen N2, at a temperature of between 1000° C. and 1300° C., preferably between 1100° C. and 1200° C. This form makes it possible to obtain a separating membrane layer made of a porous material comprising a mixture of silicon carbide and silicon nitride. The thickness of the separating membrane layer obtained is preferably between 10 and 60 micrometers. The electron microscopy and X-ray fluorescence analyses show that the material thus obtained is composed essentially of α-SiC grains bonded together by a bonding phase where the silicon nitride is concentrated.
According to a second embodiment, the filter coated with its membrane layer obtained according to the first embodiment is annealed in a temperature range extending from 600 to 1100° C., preferably between 700 and 900° C., this time under an oxidizing atmosphere, for example under air. The firing time is advantageously between 2 and 6 hours and is prolonged until there is obtained a separating membrane layer comprising this time SiC and silicon oxynitride, the formulation of which generally accepted is Si2ON2, even if other ratios are in no way excluded according to the present invention. For example, the silicon oxynitride represents between 1 and 30%, preferably between 1 and 5%, of the total weight of the material constituting the membrane.
If the filter is configured for an application in tangential filtration, it can be attached to a perforated plate at the point of the openings of channels, in leaktight manner, in order to be installed in a pipe or a filtration system. The heat treatment employed to attach the perforated plate to the filter support has to be carried out at a temperature lower than the decomposition temperature of the composite membrane.
If the filter exhibits channels which are alternately blocked in order to obtain a membrane filter which operates according to the principles of frontal filtration and if the blocking is carried out subsequent to the deposition of the membrane, at least for one face of the filter, either on the side of the inlet channels or on the outlet side, the blocking can be carried out with an SiC slip, the blocking elements being sintered at a temperature lower than the decomposition temperature of the composite membrane.
According to another configuration, not represented, of another filter according to the invention, this other filter is configured in order for the fluid to be treated to initially pass through the external wall, the permeate being collected this time at the outlet of the channels. According to such a configuration, the filtering membrane layer is advantageously deposited on the external surface of the filter and covers at least a portion of it. Such a configuration is often known as FSM (Flat Sheet Membrane). Reference may be made to the website: http://www.liqtech.com/img/user/file/FSM_Sheet_F_4_260214 V2.p df.
The figures associated with the examples which follow are provided in order to illustrate the invention and its advantages, without, of course, the embodiments thus described being able to be regarded as limiting of the present invention.
In the appended figures:
An electron microscopy photograph taken on a channel 4 of
The examples which follow are provided solely by way of illustration. They are not limiting and make possible a better understanding of the technical advantages relating to the use of the present invention.
The supports according to all the examples are identical and are obtained according to the same experimental protocol which follows.
The following are mixed in a kneader:
For each configuration, 5 to 10 crude supports with a diameter of 25 mm and with a length of 30 cm are thus synthesized.
The crude monoliths thus obtained are dried by microwave radiation for a time sufficient to bring the content of not chemically bound water to less than 1% by weight.
The monoliths are subsequently fired up to a temperature of at least 2100° C., which is maintained for 5 hours. The material obtained exhibits an open porosity of 43% and a distribution mean pore diameter of the order of 25 micrometers, as measured by mercury porosimetry.
According to this example, a separating membrane layer made of silicon carbide is subsequently deposited on the internal wall of the channels of a support structure as obtained above, according to the process described below.
A tie primer for the separating layer is formed, in a first step, from a slip, the inorganic formulation of which comprises 30% by weight of a powder of grains of black SiC (Sika DPF-C), the median diameter d50 of which is approximately 11 micrometers, 20% by weight of a powder of grains of black SiC (Sika FCP-07), the median diameter d50 of which is approximately 2.5 micrometers, and 50% of deionized water.
A slip of the material constituting the filtration membrane layer is also prepared, the formulation of which comprises 50% by weight of SiC grains (d50 of approximately 0.6 micrometer) and 50% of demineralized water.
The rheology of the slips was adjusted, by addition of the organic additives, to 0.5-0.7 Pa·s under a shear gradient of 1 s−1, measured at 22° C. according to the standard DIN C 33-53019.
These two layers are successively deposited according to the same process described below: the slip is introduced into a tank with stirring (20 revolutions/min). After a phase of deaerating under slight vacuum (typically 25 millibar) while continuing to stir, the tank is overpressurized to approximately 0.7 bar in order to be able to coat the interior of the support from its bottom part up to its upper end. This operation only takes a few seconds for a support with a length of 30 cm. Immediately after coating the slip over the internal wall of the channels of the support, the excess is discharged by gravity.
The supports are subsequently dried at ambient temperature for 10 minutes and then at 60° C. for 12 h. The supports thus dried are subsequently fired under argon at a temperature of 1430° C. for 4 h.
A cross section is taken over the filters thus obtained. The structure of the membrane is observed and studied with a scanning electron microscope.
According to this example, a separating membrane layer made of a composite silicon carbide/silicon nitride material is deposited on the internal wall of the channels of a support structure as described above and identical to that of example 1, according to the process described below.
A layer of tie primer for the separating layer is formed in a first step from a slip, the inorganic formulation of which comprises 30% by weight of a powder of grains of black SiC (Sika DPF-C), the median diameter d50 of which is approximately 11 micrometers, 15% by weight of a powder of grains of black SiC (Sika FCP-07), the median diameter d50 of which is approximately 5 micrometers, 5% of a silicon (Silgrain Micro 10), the median diameter d50 of which is approximately 3 μm, and 50% of deionized water.
A slip for the material constituting the separating membrane layer is also prepared but the formulation of which this time comprises 36% by weight of SiC grains with a median particle diameter d50 of the order of 0.6 micrometer, 4% of metallic silicon with a median particle diameter d50 of approximately 3 microns and 60% of deionized water.
The rheology of the slips is adjusted to 0.5-0.7 Pa·s at 1 s−1. In order to control the rheology of these slips and to observe a viscosity typically approximately Pa·s under a shear gradient of 1 s−1, measured at 22° C. according to the standard DIN C 33-53019. These layers are deposited according to the same process as for example 1. The coated supports are subsequently fired under nitrogen according to a temperature rise of the order of 10° C./h up to 1430° C. under stationary conditions for 4h.
According to this example, the procedure is identical to that of example 2 but 0.04% of iron oxide Fe2O3 provided by Bayferrox with a median diameter of approximately 0.7 micrometer, i.e. 0.5% with respect to the weight of silicon, is added to the slip for the material constituting the separating membrane layer.
According to this example, the procedure is identical to that of example 2 but amounts by weight of 8% of metallic silicon and 32% of SiC grains per 60% of demineralized water are introduced into the slip in order to form the material of the separating membrane layer.
Likewise, the primer layer was adapted with the same silicon content, such that its inorganic formulation comprises 30% by weight of a powder of grains of black SiC (Sika DPF-C), the median diameter d50 of which is approximately 11 micrometers, 12% by weight of a powder of grains of black SiC (Sika FCP-07), the median diameter d50 of which is approximately 5 micrometers, 8% of silicon (Silgrain Micro 10), the median diameter d50 of which is approximately 3 μm, and 50% of deionized water.
According to this example, the procedure is identical to that of example 2 but the sintering temperature is brought to 1800° C. for 2 hours under nitrogen.
According to this example, the procedure is identical to that of the preceding example 2 but the final firing of the coated supports is carried out this time at a temperature of 1100° C. for 2 hours and under pure nitrogen. This example thus appears in accordance with the teaching of the applications EP 0 219 383 and EP 2 484 433 for the preparation of an SiC membrane filter.
The properties and the characteristics of the filters thus obtained are measured as follows.
The mean thickness of the successive layers obtained for each example is measured by image analysis on the basis of the electron microscopy photographs.
The mean thickness of the separating layer is of the order of 40 micrometers for all the examples. The median pore diameter of the separating membrane layer varies between 200 and 250 nm for all the examples.
The other results as measured as indicated above are given in the following table 1.
The details of other experimental protocols followed are given additionally below:
The characteristics and the properties of the filters obtained according to examples 1 to 6 are given in table 1 below.
Other tests carried out by the applicant company have shown that the composition of the primer had no or virtually no influence on the properties described above of filtration and of durability of the separating membrane.
The results combined in the preceding table 1 indicate that examples 2 and 3 according to the invention exhibit the best combined performances in the different tests and measurements carried out. In particular, the filters having a filtering membrane according to the invention exhibit a high mechanical strength (scratch test) and also a greater filtration capacity. In addition, they appear to be more resistant to acid attacks.
According to example 5 according to the invention, it is observed that an excessively high firing temperature prevents the formation of the nitride and results finally in nitrogen contents which are too low to obtain the desired improvement. In the end, the results combined in the table indicate that the material used according to the invention to manufacture the separating membrane layer can only be obtained following certain processing conditions not yet described in the prior art.
The comparative example 6 (for which the temperature of calcination under nitrogen is only 1100° C.) exhibits a very high degree of scratching, that is to say a low mechanical strength. The data given in table 2 thus show that such a temperature, which is too low, does not make possible the insertion of elemental nitrogen into the material constituting the membrane.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1462765 | Dec 2014 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR2015/053660 | 12/18/2015 | WO | 00 |
