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Publication numberUS20020157535 A1
Publication typeApplication
Application numberUS 09/796,218
Publication dateOct 31, 2002
Filing dateFeb 28, 2001
Priority dateFeb 28, 2001
Also published asDE60211402D1, DE60211402T2, EP1236496A1, EP1236496B1, US6736882, US20030131728, US20030134742
Publication number09796218, 796218, US 2002/0157535 A1, US 2002/157535 A1, US 20020157535 A1, US 20020157535A1, US 2002157535 A1, US 2002157535A1, US-A1-20020157535, US-A1-2002157535, US2002/0157535A1, US2002/157535A1, US20020157535 A1, US20020157535A1, US2002157535 A1, US2002157535A1
InventorsVladislav Kanazirev, Alan Cohen
Original AssigneeKanazirev Vladislav I., Cohen Alan P.
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Process and adsorbent for gas drying
US 20020157535 A1
Abstract
An adsorbent and a process are disclosed for drying gases in a pressure swing dryer. The adsorbent comprises a pre-formed alumina particle with a thin layer of colloidal silica disbursed on the surface of the preformed alumina particle. Surprisingly the thin layer of colloidal silica does not interfere with the drying properties of the pre-formed alumina particle, while significantly improving the physical properties of the pre-formed alumina particle
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Claims(19)
What is claimed is:
1. A process for the drying of a compressed gas comprising a gas component and water, said process comprising contacting the compressed gas stream with an adsorbent to adsorb at least a portion of the water to produce a dry compressed gas stream, wherein said selective adsorbent comprises a shaped alumina particle having dispersed thereon a colloidal silica layer.
2. The process of claim 1 wherein the adsorbent has an attrition loss of less than 0.04 wt-%.
3. The process of claim 1 wherein the silica layer extends less than about 50 microns from the surface of the shaped particle towards the center of the particle.
4. The process of claim 1 wherein the adsorbent comprises a rehydration loss of less than about 5 wt-%.
5. The process of claim 1 wherein the shaped alumina particle is selected from the group consisting of spherical, an extrudate, a pill, a flake or a monolith.
6. The process of claim 1 wherein the gas component is selected from the group consisting of air, nitrogen, light hydrocarbons and mixtures thereof.
7. The process of claim 1 wherein the gas component comprises air.
8. The process of claim 1 further comprising periodically purging the selective adsorbent to desorb the water.
9. The process of claim 1 wherein the contacting of the compressed gas with the adsorbent takes place in a pressure swing adsorption process wherein the adsorbent is depressurized to an effective desorption pressure and purged to desorb the water.
10. A method for producing an adsorbent for drying compressed gas comprising:
a) coating a pre-formed alumina particle with a coating solution comprising colloidal silica to provide a coated pre-formed particle having a narrow layer of colloidal silica disbursed thereon; and
b) drying and activating the coated pre-formed particle to produce the adsorbent.
11. The method of claim 10 wherein the pre-formed particle comprises a sphere or an extrudate.
12. The method of claim 10 wherein the coating solution also comprises an ion selected from the group consisting of sodium, chloride, hydrogen, and the like.
13. The method of claim 10 wherein the coated pre-formed particle is activated at an activation temperature greater than about 400° C. (750° F.).
14. A shaped particle having a core consisting of a shaped alumina carrier having a colloidal silica layer dispersed on the shaped alumina carrier, at least 60 percent of the colloidal silica being present in a band extending from the surface towards the center and having a width of less than about 50 microns.
15. The shaped particle of claim 14 wherein the band of colloidal silica extending from the surface toward the center comprises a width of less than about 20 microns.
16. The shaped particle of claim 14 wherein the adsorbent has an attrition loss of less than 0.4 wt-%.
17. The shaped particle of claim 14 wherein the adsorbent comprises a rehydration loss of less than about 5 wt-%.
18. The shaped particle of claim 14 wherein the shaped alumina particle is selected from the group consisting of a sphere, an extrudate, a pill, a flake or a monolith.
19. An air brake dryer assembly having a refillable or replaceable cartridge containing the shaped particle of claim 14.
Description
FIELD OF THE INVENTION

[0001] The present invention relates, in general, to a process for drying a compressed gas stream and, more particularly, to a process for drying a gas stream with a novel solid adsorbent.

BACKGROUND OF THE INVENTION

[0002] Drying of gases to remove water is a common requirement in providing gases at high pressure for use in chemical processing, air brake systems in transportation, and shop applications ranging from pneumatic control to paint spraying. The removal of moisture from the high pressure gases reduces corrosion and prevents water buildup and freezing in such systems. Condensation of water in air brake systems or pneumatic systems can result in inefficiencies and system failure.

[0003] In fluid drying and purification applications in which a contaminant is present in the fluid at concentrations of about 3 percent or less, the adsorbent is generally of low value and frequently removed for disposal. One important drying and purification application includes drying air, particularly compressed air. In such applications cost can become a significant factor in the selection of a drying process. For example, a once-through process employs an adsorbent which is exposed to the fluid until the adsorbent is no longer effective in removing the contaminant Once-through processes require large inventories of adsorbent and frequent disposal of spent adsorbent An alternative to this approach is to employ a regenerative adsorption cycle wherein the adsorbent is periodically regenerated to remove the contaminant from the spent adsorbent and restore the adsorbent's capacity for adsorbing the contaminant. Regenerative adsorption cycles are generally classified according to the manner in which the desorption takes place Both thermal swing adsorption processes and pressure swing adsorption processes are generally known in the art for various types of adsorptive separations. Generally, thermal swing processes utilize the process steps of adsorption at a low temperature, regeneration at an elevated temperature with a hot purge gas and subsequent cooling down to the adsorption temperature. One process for drying gases generally exemplary of thermal swing processes is described in U.S. Pat. No. 4,484,933, issued to Cohen. The patent describes basic thermal swing processing steps coupled with the use of an auxiliary adsorber bed for improving the regeneration step Thermal swing processes are often used for drying gases and liquids and for purification where trace impurities are to be removed. Often, thermal swing processes are employed when the components to be adsorbed are strongly adsorbed on the adsorbent, i.e., water, and thus, heat is required for regeneration. Thermal swing adsorption processes are characterized by long cycles which require large amounts of purge gas to regenerate and cool the adsorbent to return the adsorbent to adsorption conditions in each cycle.

[0004] Pressure swing adsorption (PSA) provides a means for adsorption that does not require heat for regeneration. Instead, regeneration is accomplished by reducing the pressure in the adsorber bed to below the pressure at which adsorption had occurred. PSA process typically includes steps of adsorption at an elevated pressure, desorption to a lower pressure and repressurization to the adsorption pressure. The process also often includes a purge step at the desorption pressure to enhance desorption. PSA processes are characterized by lower adsorbent differential loadings within each cycle which results in greater inventories of adsorbent Furthermore, the cycle time of a PSA process is shorter than a thermal swing adsorption process because there are no heat transfer related delays while the bed is cooled to adsorption conditions. Lastly, the amount of purge gas required for a PSA process can be significantly lower than the amount of purge gas in a thermal swing adsorption process, because the purge gas in the PSA process is only required to remove adsorbate from the adsorbent and not to additionally cool the adsorbent.

[0005] Such PSA processing is disclosed in U.S. Pat. No. 3,430,418 issued to Wagner and in U.S. Pat. No. 3,986,849 issued to Fuderer et al, wherein cycles based on the use of multi-bed systems are described in detail As is generally known and described in these patents, the contents of which are incorporated herein by reference as if set out in full, the PSA process is generally carried out in a sequential processing cycle that includes each bed of the PSA system. Such cycles are commonly based on the release of void space gas from the product end of each bed in one or more cocurrent depressurization steps upon completion of the adsorption step. In these cycles, the released gas typically is employed for pressure equalization and for subsequent purge steps. The bed is thereafter countercurrently depressurized and often purged to desorb the more selectively adsorbed component of the gas mixture from the adsorbent and to remove such gas from the feed end of the bed prior to the repressurization thereof to the adsorption pressure.

[0006] Pressure swing dryers are used on heavy trucks and busses to dry the compressed air that operates the brakes and other pneumatic accessories. These dryers use molecular sieve or other desiccants to remove water from ambient air that has been compressed to usually about 130 psig (8.8 bar gauge). Some trucks now operate systems with 12 bar gauge (176 psig) of air pressure. The dryers operate on a pressure swing cycle. Compressed ambient air is passed into the air brake dryer unit, wherein liquid water is separated and water vapor is adsorbed on a desiccant. Dry, compressed air is removed from the air brake dryer unit and passed to the brake system. Water is desorbed from the desiccant in a desorption or depressurization step which typically takes place at atmospheric pressure, 0 bar (gauge pressure) and may include a purge step at atmospheric pressure.

[0007] In air brake systems, the compressor runs intermittently in cycles determined by the filling and depletion of the air in a supply tank. The compressor pumps until the pressure in the supply tank reaches the cut out pressure or upper pressure limit, typically about 1000 kPa (145 psia). Then the compressor rests until the pressure in the supply tank is reduced by air usage in the brake systems, other pneumatic equipment and regeneration (purging) of the dryer, falls to the lower pressure limit reaches about 860 kPa (125 psia).

[0008] An alumino-silicate gel desiccant, for example, is commonly used as a drying agent for extracting water vapor from gas. This desiccant has a strong molecular attraction for water vapor and may require heating to about 250°to 400° F. (120° to 205° C.) to fully desorb water vapor. It has been observed that alumino-silicate gel desiccant also will adsorb VOC's and may require heating up to about 350° F. (about 175° C.) or more to fully desorb typical VOC's released in a paint spray booth. Low boiling point hydrocarbons are desorbed at a lower temperature than higher boiling point hydrocarbons. When either water vapor or VOC's are directly adsorbed by a desiccant, a strong dipole bond is formed. One desiccant for adsorbing VOC's is an alumino-silicate gel containing about 3% alumina (Al2O3) and 97% silica (SiO2) in the form of hard, generally spherical beads. Such a desiccant is commercially available, for example, from Engelhard Corporation of Iselin, N.J. under the trademark “Sorbead®”.

[0009] Pressure swing dryers contain a desiccant, which alternately adsorbs water from the compressed air and then desorbs the water into the purge air. Molecular sieves, silica gel, activated alumina, and alumino-silicate gels as disclosed hereinabove are all used commercially as pressure swing desiccants. Other VOC adsorbent materials such as zeolite also may be acceptable alternatives (see U.S. Pat. No. 5,968,235). In addition to the ability to adsorb and desorb water, a pressure swing desiccant should have suitable physical properties (attrition, abrasion, and dust) and low cost, Low reactivity with hydrocarbons is also desirable. Silica gel is a low cost alternative, but generally suffers from breakage when contacted with liquid water. Activated alumina is also a low cost alternative, but suffers from high abrasion loss and dust. Molecular sieves are effective, but cost much more than silica gel or alumina. The alumino-silicate gel consisting of 3% alumina and 97% silica is more costly than activated alumina and is highly reactive to unsaturated hydrocarbons than molecular sieves, silica gel or alumina.

[0010] There is a need for low cost, effective adsorbents for use in pressure swing adsorption air dryers. A suitable adsorbent must not only produce low dew points, it must also have acceptable physical properties, such as low dust and resistance to abrasion loss and attrition. Air brake drying represents a severe environment for the operation of a dryer wherein the desiccant is subject to vibration and large pressure swings between the adsorption and desorption steps. In addition, the desiccant is exposed to hot compressed air which may contain oil and other volatile compounds such as hydrocarbons which could harm brake cylinders and related equipment. Adsorbents are sought which are more resistant to attrition and abrasion loss than conventional materials and which are effective in the removal of water and other contaminants from the compressed gas to produce dry compressed gases, i.e., compressed gases having a low dew point.

SUMMARY OF THE INVENTION

[0011] The present invention provides a desiccant and a process for drying a gas comprising a gas component such as air, light hydrocarbons, nitrogen, hydrogen, and mixtures thereof and water. The present invention can be employed to provide improved systems for drying compressed gases, for such applications as air brake drying in truck and locomotive brake systems, and in providing dry compressed gases for shop use. According to the present invention, activated shaped or pre-formed alumina particles are modified by depositing a thin dispersed layer of colloidal silica on the external surface of the alumina particles The colloidal silica coating drastically reduces the abrasion loss and dusting. Surprisingly, this improvement is achieved without seriously reducing the drying performance of alumina. Furthermore, the colloidal silica-coated alumina of the present invention has low reactivity to unsaturated hydrocarbons because the surface coating of colloidal silica minimizes contact between the unsaturated hydrocarbons and the deactivated alumina surface.

DETAILED DESCRIPTION OF THE INVENTION

[0012] The process of the invention is intended to be practiced on feed gas streams which comprise a feed gas and moisture or water; such feed gas streams include air, nitrogen, light hydrocarbons and mixtures thereof. The term “light hydrocarbons” is intended to include hydrocarbons having 1 to 4 carbon atoms per molecule.

[0013] The process of the present invention is useful in gas drying applications such as in air brake systems for trucks or locomotives In these systems the gas, such as air, is generally saturated with water following its compression to some operating pressure to activate the braking systems of the vehicle or piece of heavy equipment If this water is not removed or significantly reduced, the braking systems will be subject to greater corrosion, or freezing, resulting in higher maintenance costs and reduced reliability Generally, the feed gas stream employed to activate a braking system comprises air at water saturation conditions and a pressure above atmospheric pressure. Preferably the temperature at which the feed gas stream is available ranges between about 37° C. (100° F.) and about 82° C. (180° F.). More preferably the temperature at which the feed gas stream is available ranges between about 37° C. (100° F.) and about 66° C. (150° F.). Preferably the pressure at which the feed stream is available is greater than about 790 kPa (100 psig), and more preferably the pressure at which the feed gas stream is available ranges between about 790 kPa and about 1.14 MPa (150 psig), and most preferably the pressure at which the feed gas stream is available ranges between about 790 kPa and about 869 kPa (110 psig).

[0014] The water in the feed gas stream, or compressed gas stream, will be present at saturated conditions which comprise from about 8,000 to about 32,000 ppm-vol depending upon the temperature and the pressure of the feed gas. Preferably the water content in the product gas, or dry compressed gas, produced by the dryer will be reduced by at least about 95 percent, and more preferably the water content in the product gas will be reduced by about 95 to about 99.9 volume percent of the amount of water in the feed gas. Preferably the amount of water in the product gas stream will be less than 1000 ppm-vol, and more preferably the amount of water in the product gas stream will range from about 50 to about 100 ppm-vol. In some cases the water content of the product gas will be expressed as the dew point depression from the ambient air temperature, wherein the dew point depression is the ambient temperature minus the dew point temperature for any stream. The dew point temperature for any stream is the temperature at which condensation will occur. In such cases, the dew point depression preferably will be greater than about 17° C. (30° F.) and more preferably will be greater than about 50° C. (90° F.).

[0015] The term “pressure swing adsorption” as used herein generally relates to an adsorption process wherein an adsorber bed is part of an integrated process whereby a continuous adsorber operation can be obtained while simultaneously regenerating a spent adsorber bed. In pressure swing adsorption, there exists a plurality of adsorption zones maintained at an elevated pressure effective to adsorb water while allowing the bulk of the feed gas to pass through the adsorber bed. At a defined time, the passing of the adsorber feed to a first adsorber bed is discontinued and the first adsorber bed is depressurized by one or more counter-current depressurization steps wherein the pressure is reduced to a defined level which permits additional components of the feed gas remaining in the first adsorber bed to be withdrawn and utilized or vented The first adsorber bed is depressurized in a countercurrent depressurization step wherein the pressure in the first adsorber bed is further reduced by withdrawing desorbed water vapor countercurrently to the direction of the feed. Finally the adsorber bed is purged with a purge gas such as dried product gas and repressurized. The final stage of repressurization is with the feed gas or the product gas in order to conserve the feed or the product gas.

[0016] In air brake drying systems, the process is simplified and generally there are no feed gas conservation steps. Pressure swing adsorption in air brake drying is generally carried out in a single adsorbent bed with essentially two process steps. The adsorption stroke comprises rising pressure adsorption as the feed gas is introduced and the adsorber bed pressure rises to the pressure of the feed gas, followed by constant pressure adsorption as the feed gas is passed through the adsorber bed and a product gas is collected in a product reservoir. The adsorption stroke is continued until a pressure set point in the product reservoir is reached which corresponds to the capacity of the reservoir. Typically this pressure set point is about 930 kPa (135 psia) and is reached after about 2 minutes in heavy services or in about 30 seconds under light duty. At this point, the feed gas passing is discontinued and the adsorber bed is placed in a desorption stroke wherein the adsorber bed is simultaneously counter-currently depressurized and purged with a portion of the product gas withdrawn from the product reservoir. Typically the portion of the product gas is collected during each cycle in the product reservoir, or pressurized storage tank, and the desiccant or adsorbent is disposed in a replaceable or refillable cartridge in an air brake dryer assembly. At the completion of the desorption stroke, the pressure swing air dryer is returned to the adsorption stroke. A cycle time for pressure swing air brake drying means the length of time of the adsorption stroke plus the length of the desorption stroke. Typically the cycle times for such pressure swing air brake dryers ranges from about 60 seconds to about 150 seconds. The pressure swing air brake dryers are fixed beds containing an adsorbent and are configured with low length to diameter ratios to accommodate vehicle space limitations. In some severe service situations for example in locomotives, pressure swing adsorption air brake systems are provided with 2 adsorption beds which alternate between the adsorption and desorption strokes to provide a continuous supply of dry air. An example of an air brake dryer containing a desiccant is disclosed in U.S. Pat. No. 5,607,500, which is hereby incorporated by reference.

[0017] Pressure swing adsorption systems are more efficient at higher pressures, typically pressures greater than about 2.2 MPa (300 psig), In addition, pressure swing adsorption air brake dryers are generally characterized by short cycles with relatively low differences in adsorbent loading between the upper and lower pressure ranges of operation. This leads to the use of larger amounts of adsorbent in a pressure swing adsorption device than a thermal swing adsorption process. Furthermore, the amount of purge gas required for a pressure swing adsorption unit varies inversely with pressure; the ratio of purge gas to feed gas is reduced as the pressure increases. At low pressures, the amount of purge gas approaches the amount of feed gas.

[0018] The adsorbent of the present invention is prepared by treating shaped alumina particles with colloidal silica prior to activation. The activated alumina referred to includes alumina having a surface area usually greater than 100 m2/g and typically in the range of 100 to 550 m2/g. Further, the activated alumina powder is preferably obtained by rapid dehydration of aluminum hydroxides, e.g., alumina trihydrate or hydrargillite in a stream of hot gases. Dehydration may be accomplished in any suitable apparatus using the stream of hot gases. Generally, the time for heating or contacting with the hot gases is a very short period of time, typically from a fraction of a second to 4 or 5 seconds, for example. Normally, the temperature of the gases varies between 400°and 1000° C. The process is commonly referred to as flash calcination and is disclosed in U.S. Pat. No. 2,915,365 incorporated herein by reference. However, other methods of calcination may be employed to dehydrate or partially dehydrate the trihydrate.

[0019] A source of activated alumina is gibbsite which is one form of alumina hydrate derived from bauxite using the Bayer process. However, alpha alumina monohydrate, pseudoboehmite or the alumina trihydrate may be used. Other sources of alumina may also be utilized including clays and aluminum alkoxides. Also, alumina gel may be used as a source of the alumina. The shaped or pre-formed alumina particles are agglomerates having an average pore diameter less than about 3.5 nm (35 angstroms). The agglomerates may be formed into spheres, pills, extrudates, flakes, monoliths and the like. Agglomerates formed in this manner generally comprise alumina particles having an average particle diameter of about 9,000 to 10,000 nm. The total surface area of a typical alumina particle will be about 350 m2/g, while the surface area of the surface only of the alumina particle is about 12 m2/g. The adsorbent of the present invention comprises alumina particles having colloidal silica disposed on the surface of the alumina particles without obstructing the remaining surface area within the porous alumina particle. This phenomena was confirmed by scanning electron microscopy and energy dispersive x-ray analysis (SEM-EDS). When the shaped alumina particles which range in size from about 1.0 to about 3.0 mm are treated with colloidal silica, the silica is disposed in a narrow layer or band concentrated near the surface of the shaped alumina particle. Surprisingly, this narrow band of silica does not interfere with the adsorption properties of the shaped or pre-formed alumina particle, and actually improves the physical properties of the adsorbent including attrition loss and abrasion. The colloidal silica could be applied to the pre-formed alumina particle by spraying, soaking or any other conventional means. It is preferred to apply the colloidal silica layer by soaking the pre-formed alumina particle in a colloidal silica solution.

[0020] A colloid is defined as consisting of small particles which are in suspension which fails to settle out and diffracts a beam of light. By the term “colloidal silica” it is meant silica particles ranging in average diameter greater than 4 nm and less than about 500 nm. Preferably, the average diameter of the colloidal silica particles ranges from about 4 nm to about 200 nm, and most preferably the average diameter of the colloidal silica particles ranges from about 4 nm to about 10 nm, A preferred colloidal silica solution comprises colloidal silica in an aqueous solution. The colloidal silica solution can comprise other ions selected from the group consisting of sodium ions, hydrogen ions, chloride ions, and the like. In the present invention, the colloidal silica does not penetrate the entire particle, but remains within a thin layer near the surface of the pre-formed alumina particle. On the other hand, silicate treating; that is, treating with soluble silica, results in silica dispersed beyond the surface toward the center of the pre-formed alumina particle. Such silicate treated materials do not show the improved physical properties such as attrition loss and abrasion of the adsorbent of the present invention.

[0021] One of the problems of coating silica on pre-formed particles of alumina is keeping the coating on the alumina particle, This ability of the coating to remain on the particle is measured by attrition loss and by abrasion loss. Attrition loss is a physical property of the pre-formed alumina particle which is measured by rubbing or grinding the particles together and measuring the loss during the grinding process. Accordingly, a sample of the material is rotated for a set period of time in a cylindrical drum having a single baffle. Any fines produced during the test are determined and considered to be a measure of the propensity of the material to produce fines in the course of transportation, handling and use. Typically, 100 g of material are rotated for 1800 revolutions at a rate of about 60 revolutions per minute. The colloidal silica coated alumina particles of the present invention surprisingly showed a significant reduction in attrition loss relative to untreated and silicate treated alumina particles. The attrition loss after colloidal silica treatment was less than 0.5 wt-% and more particularly the attrition loss of the colloidal silica treated alumina was less than 0.2 wt-%. This represents a 400% improvement over conventionally silicate treated and untreated alumina.

[0022] Abrasion loss is measured by placing a weighted sample of material on a screen and tapping the screen for about 30 minutes while catching any dust produced The amount of dust produced is determined and expressed as a weight percent loss. Abrasion loss determined for the colloidal silica treated alumina particles showed significant improvement over conventional silica treated and untreated aluminas. The abrasion loss for colloidal silica treated alumina particles was less than 0.5 wt-%, and more particularly less than 0.05 wt-%

EXAMPLES

[0023] The following examples are provided to illustrate the process of the present invention and are not intended to limit the scope of the claims that follow. The examples are based on laboratory data of adsorption characteristics of various desiccants or on process engineering design calculations and adsorption relationships as noted. Some of the examples presented below are experiments done with unactivated, pre-formed alumina particles as described hereinabove. They are formed in a conventional manner by agglomerating flash calcined alumina as described hereinabove.

Example 1

[0024] (Spray Treatment)

[0025] About 1000 g of unactivated, pre-formed alumina particles of 2.4 to 4 mm in diameter (size 5×8 mesh Tyler screen series) were treated in a 0.3 meter (12-inch) laboratory rotating drum and sprayed by hand with the following solutions. The method used was to spray the pre-formed alumina particles for 3-5 minutes with 70-80 cc of the silica solution followed by about 5 minute further rotation. The alumina particles were then tray activated for 1 hour at 750° F. (400° C.) in a Grieve oven and analyzed for attrition according to the American Society for Testing and Measurement (ASTM) test designation D 4058-87. Abrasion was also measured to determine the abrasion loss of activated alumina wherein a 165 g sample is placed on a 595 micron (28 mesh Tyler) screen and the screen is tapped for 30 minutes. Abrasion loss is the weight percent of sample lost through the screen.

TABLE 1
Approx. Abrasion
Treatment SiO2 content Loss, SPM Attrition, ASTM
Sample Solution (VFB*) 202B, wt-% D4058-87, wt-%
1-1 None 0   0.66 0.85
1-2 Water 0   0.62 0.77
1-3 Na2SiO3 2.2 1.03 0.89
1-4 Ludox ® Cl 2.1  0.048 0.10
1-5 Ludox ® SM 1.8 0.04 0.21

[0026] Ludox® C1 (DuPont Corp. identified as Ludox® CL) is a colloidal silica coated with alumina and containing chloride as an ion. The Ludox® CL has a total content of SiO2 and Al2O3 of about 30 wt-%, and a pH of 4.6. Ludox® SM (DuPont Corp. identified as Ludox® SM-30) is sodium-stabilized 30 wt-% colloidal silica, with a pH of 10.5. The spraying solution for samples (1-4) and (1-5) was prepared by diluting the original Ludox® reagent with an equal mass of water. A weight of 92.7 g of diluted Ludox® Cl solution was sprayed over 1000 g pre-formed alumina particles to make sample (1-4), and 78.6 g of diluted Ludox® SM was sprayed over 1000 g of pre-formed alumina particles to make sample (1-5).

[0027] Sodium metasilicate Na2SiO3·5 H2O is a technical grade reagent available from Alfa Aesar. Forty grams of the granular product was dissolved in 100 g water. The pre-formed particles (1000 gm) were sprayed with 108 g of sodium metasilicate solution to make sample (1-3).

[0028] The abrasion loss for the water treated control sample (1-2) is practically the same as the untreated particles of sample (1-1). The abrasion loss of the alumina particles treated with both forms of colloidal silica samples (1-4) and (1-5) are improved by more than one order of magnitude, while the abrasion loss with the sodium silicate sample (1-3) actually became worse, indicating that the silicate coating may be contributing to the abrasion loss. The samples treated with colloidal silica were significantly reduced in attrition loss under the ASTM test of 1800 revolutions of the test drum.

[0029] In Example 1, the treatment with colloidal silica has apparently produced a narrow layer of silica around the alumina particle that protects the outer surface from loss of material by attrition and abrasion. It is surprising that sodium silicate is distributed more evenly through the alumina core and is ineffective in producing an outer layer with the associated benefits.

Example 2

[0030] (Rehydration of Silica Treated Pre-formed Particles)

[0031] The pre-formed alumina particles treated with solutions in Example 1 were further analyzed by thermal gravimetric analysis (TGA) a few hours after the treatment, stored at room temperature in closed glass vials, and re-analyzed after 11 days. A differential TGA plot of weight loss vs. temperature gives insight into the alumina phases that are present in the sample. Of particular interest is the phase change or “rehydration” of the alumina to aluminum hydroxide [Al(OH)3]. Aluminum hydroxide gives a water loss at 270° C., whereas alumina does not. Based on the area under the peak of the differential TGA plot at about 300° C., rehydration was estimated as follows:

TABLE 2
Rehydration Effects on Alumina Particles
Conversion to AL(OH)3 with time
Conversion to Conversion to
Approx. SiO2 Al(OH)3, %, Al(OH)3, %,
Sample content (VFB*) Same day After 11 days
1-2 0   1.0 7.0
1-3 2.2 2.0 7.5
1-4 2.1 3.8 3.8
1-5 1.8 1.0 3.8

[0032] The data show that treatment with colloidal silica in samples (14) and (1-5) enhanced the stability of the pre-formed alumina particles and resulted in a significantly reduced tendency for rehydration, relative to the untreated and silicate treated alumina.

Example 3

[0033] (Stability Towards Rehydration of Activated Alumina Particles)

[0034] The pre-formed alumina particles produced in Example 1 were activated at 750° F. (400° C.) in an oven. Then 70 g of activated particles were added to 90 g deionized water and stored at room temperature for a prolonged period of time. Small samples were withdrawn and analyzed by TGA to determine the degree of rehydration. The results are shown in Table 3.

TABLE 3
Rehydration Stability
Rehydration Rehydration Rehydration
Sample after 24 h after 90 h after 240 h
1-1 5.1 9.7 15.0
1-2 4.0 9.5 14.2
1-3 5.5 8.5 12.0
1-4 3.3 7.6 12.6
1-5 4.2 8.8 12.4

[0035] The data on the activated particles in Table 3 show that all the silica-coating materials, including sodium silicate and both colloidal silicas, reduced the rehydration tendency of alumina. After 240 hours in water, the untreated (1-1) and water-treated (1-2) lost more than 14 wt-% of the alumina to rehydration, but the silica-treated particles lost only 12 wt-%, an improvement of about 15% after 240 hours, which is unexpected The expected result would have been that only the SiO2-coated portion of the coated pre-formed alumina particle would resist re-hydration. The expected improvement in re-hydration would be just about 3 5 wt-% for the 20-micron penetration of SiO2 into the particle observed in Example 5 below.

Example 4

[0036] (BET Surface Area)

[0037] The pre-formed alumina particles treated in Example 1 and activated at 750° F. were tested for BET surface area. The results, given in Table 4, show that the surface area was retained in spite of the silica coating. This shows that the coating did not form an impermeable envelope around the pre-formed alumina particles.

TABLE 4
Treatment Approx. SiO2 BET Surface
Sample Solution content (VFB*) Area, m2/g
1-2 Water 0   359
1-3 Na2SiO3 2.2 (not measured)
1-4 Ludox ® Cl 2.1 356
1-5 Ludox ® SM 1.8 366

Example 5

[0038] (Location of Silica Species)

[0039] The location of the silicate species in the treated particles of Example 1 was investigated by SEM-EDS scanning electron microscopy and the silica content was determined within a particle by energy dispersive analysis by x-rays. Measurements were made across the interior of the particle to determine the silica distribution of a sectioned particles of about 3.5 mm in diameter. The presence of silica as SiO2 in weight percent was plotted against the distance from the outer surface of the particles in the FIGURE. The nomenclature here is the same as in Example 1. These data show that a colloidal silica layer was formed on the outer surface by the treatment with colloidal silicas. The Ludox® C1 produced a silica layer that penetrated only about 20 microns into the particle. The Ludox® SM deposited more SiO2 on the outside, and its concentration also trailed off at about 20 microns, but a small amount penetrated farther into the particle to about 140 microns. The sodium silicate was more evenly distributed in the outer 140 microns of the particle.

Example 6

[0040] (Soaking vs. Spraying Colloidal Silica)

[0041] In another preparation, a sodium stabilized colloidal silica solution (30% silica) (available from Nalco Chemical as Nalco® 1130) was applied to 3.5 to 6.7 mm (3×6 mesh) pre-formed alumina particles by spraying and soaking The amount of colloidal silica applied is shown in Table 5 below:

TABLE 5
Treatment Treatment Silica Added, Abrasion Loss,
Sample Solution Method wt-% (VFB*) SPM 202B, wt-%
6-1 Water Soak 0   0.35
6-2 Nalco ® 1130 Soak 0.8 0.17
6-3 Water Spray 0   1.33
6-4 Nalco ® 1130 Spray 2.2 0.15

[0042] Sample (6-3) was prepared by spraying 900 gm of pre-formed alumina particles with 78.7 gm water. Sample (6-4) was prepared by spraying 900 gm of pre-formed alumina particles with 62.1 gm diluted Nalco® colloidal silica solution. The diluted colloidal silica solution was prepared by mixing Nalco® 1130 with an equal mass of deionized water The soaking was done with water (1000 gm pre-formed alumina particles with 500 gm water for sample (6-1)) and colloidal silica (800 gm pre-formed alumina particles with 400 gm liquid consisting of 50 gm undiluted Nalco® 1130, 30% colloidal silica solution and 350 gm water for sample (6-2)). In both cases, the soaking solution just covered the pre-formed alumina particles placed in a beaker. After allowing the pre-formed alumina particles to stand without stirring for about 25 minutes, the liquid was decanted. Both the sprayed and soaked pre-formed alumina particles were further de-watered by being spread over a screen tray and immediately activated at 400° C. (750° F.) for one hour. The results show that merely soaking in water is effective in reducing abrasion loss, compared to spraying with water. However, spraying or soaking with colloidal silica are significantly more effective in reducing abrasion loss by more than 200% over treatment with water.

Example 7

[0043] (Dust Measurement)

[0044] Pre-formed alumina particles having an average diameter of between 1.4 mm and 2.8 mm (7×12 mesh) were treated by spraying with water, diluted with 30% colloidal silica, and sodium silicate, and then activated at 750° F. As in Example 6, the diluted colloidal silica solution was prepared by diluting the 30% colloidal silica solution of Example 6 with an equal mass of water. The dust level of the samples was reduced significantly by spraying with colloidal silica compared to spraying with water. Unexpectedly, sodium silicate treatment actually increased the dust level of the particles.

TABLE 6
Solution Treatment Silica Added, Relative
Sample Treatment Method wt-% (VFB*) Dust
7-1 Water Spray 0   466
7-2 30% Colloidal Silica Spray 1.6  80
7-3 Na2SiO3 Spray No data 753

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US7332017 *Sep 24, 2004Feb 19, 2008The Boc Group, Inc.Method and apparatus for separation of moisture from fluids
US7850766 *Aug 31, 2006Dec 14, 2010Cocona, Inc.Systems and methods for preferentially heating active particles and articles produced thereof
US7981836 *May 24, 2006Jul 19, 2011Uop LlcHydrothermally stable alumina
US8076263 *Sep 12, 2007Dec 13, 2011W. R. Grace & Co.-Conn.Sulfur tolerant alumina catalyst support
US8278242 *Jan 17, 2011Oct 2, 2012Uop LlcHydrothermally stable alumina
US20110053478 *Mar 19, 2009Mar 3, 2011Saint-Gobain Centre De Recherches Et D'etudes EuropeenFused and coated silica grains
US20110111955 *Jan 17, 2011May 12, 2011Uop LlcHydrothermally stable alumina
Classifications
U.S. Classification95/96, 502/407, 95/117, 502/415
International ClassificationB01J20/30, B01J20/10, B01D53/26, B01D53/28, B01J20/08, B01J20/32, B01D53/047, B60T17/00, B01D53/04, B01J20/34
Cooperative ClassificationB01D53/0415, B01D53/261, B01J20/3293, B01D53/047, B01D2253/342, B01D2259/4143, B01J20/08, B01J20/28019, B01D2253/106, B01J20/28016, B01D2253/104, B01J20/103, B01D53/02, B01J20/28061, B01J20/3236, B01D2257/80, B60T17/004, B01J20/3078, B01J20/3204, B01J2220/62, B01J20/28042
European ClassificationB01J20/32B4, B01J20/32F4, B01J20/32H4, B01J20/32F4D, B01J20/30, B01J20/10B, B01J20/32, B01D53/26B, B60T17/00A1, B01D53/047, B01J20/08, B01D53/02