Composite adsorbents and method of making them

Abstract

A composition for making composite adsorbents from a mixture of geopolymer, zeolite and activated carbon wherein a geopolymer material, a carbonaceous material, and an alkali activating agent are the components of the mixture. The alkali activating agent to carbonaceous material solid mass ratio is at least 0.25:1, respectively. A process for producing shaped composite adsorbents from the composition is done using conventional means such as mixing, shaping, extrusion and other methods. Alkali activation is used to convert the carbonaceous material to activated carbon, followed by hydrothermal treatment to convert the geopolymer material to zeolites. Shaped composite adsorbents fabricated from the composition of the instant invention are used for adsorption, purification, or other separation applications of liquids and gases.

Claims

1. A process for producing composite adsorbents having components of geopolymer, zeolite, and activated carbon, comprising: (a) mixing a geopolymer material which comprises an aluminosilicate source, an alkali silicate activator, and a carrier fluid in the composition, a carbonaceous material, and an alkali activating agent, wherein the alkali activating agent to carbonaceous material solid mass ratio is at least 0.25:1, respectively, to produce a paste mixture wherein the paste mixture has a uniform composition and desired rheology for shaping, (b) fabricating the paste mixture using common adsorbent shaping methods to form granule or pellet compositions possessing sizes from 0.2 to 5 mm for adsorption processes, (c) curing the granule or pellet compositions to increase strength through geopolymerization, (d) chemically activating the carbonaceous material in the granule or pellet compositions at a temperature of greater than about 400° C. in an inert gas using the alkali activating agent present in the compositions to in-situ produce activated carbon, (e) conducting hydrothermal treatment of the composition to convert part of the geopolymer to in-situ produce zeolite and form the composite adsorbents, and (f) washing and drying the produced composite adsorbents.

2. The process of claim 1 (a), wherein the geopolymer material is a class of aluminum silicate inorganic polymers which have an amorphous 3-dimensional polysialate network consisting of SiO.sub.4 and AlO.sub.4 tetrahedra.

3. The process of claim 1 (a), wherein the carrier fluid is water.

4. The process of claim 1 (a) wherein the carbonaceous material is coal, petroleum coke, charcoal, petroleum asphalt, waste rubber tire, or biomass.

5. The process of claim 1 (a), wherein the alkali activating agent is an alkali metal or alkaline earth metal hydroxide or salt.

6. The process of claim 5, wherein the alkali metal hydroxide is at least one of sodium hydroxide, potassium hydroxide, or lithium hydroxide.

7. The process of claim 5, wherein the alkali activating agent is sodium hydroxide.

8. The process of claim 1 (a), wherein the ratio of the alkali activating agent to carbonaceous material solid mass ratio is at least 0.5:1.

9. The process of claim 1 (a), wherein the ratio of the alkali activating agent to carbonaceous material solid mass ratio is at least 1:1.

10. The process of claim 1 (d), wherein the inert gas is nitrogen.

11. The process of claim 1 (c), wherein the curing is done at a temperature from about 20 to about 150° C., conducted over 1 to 72 hours.

12. The process of claim 1 (c), wherein the curing in done in the presence of moisture, water or steam.

13. The process of claim 1 (d), wherein the temperature is from about 400 to about 1,000° C.

14. The process of claim 1 (e), wherein the temperature of the hydrothermal treatment is below about 250° C. and is done in the presence of water or an alkali solution.

15. A composite adsorbent comprising a mixture of geopolymer, zeolite, and activated carbon whenever produced by the process of claim 1.

16. A process for preparing a composite adsorbent having a geopolymer, zeolite, and activated carbon, wherein the improvement comprises the steps of: (a) preparing a geopolymer material which comprises an aluminosilicate source, an alkali silicate activator, and a carrier fluid in the composition, (b) chemically activating a carbonaceous material in a granule or pellet composition form, at a temperature of greater than about 400° C., in an inert gas, using an alkali activating agent present in the compositions to in-situ produce activated carbon, and (c) conducting hydrothermal treatment of the composition of step (a) to convert part of the geopolymer to in-situ produce zeolite and form the composite adsorbent.

17. The process of claim 16 (a), wherein the temperature is from about 400 to about 1,000° C.

18. The process of claim 16 (b), wherein the temperature of the hydrothermal treatment is below about 250° C. and is done in the presence of water or an alkali solution.

19. The process of claim 1 (b), wherein the adsorbent shaping methods are granulation or extrusion.

20. The process of claim 4, wherein the biomass is derived from wood, bamboo, coconut husk, lignite, or rice husk.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 illustrates as a flow diagram the process steps for manufacturing the composite adsorbents of the instant invention.

(2) FIGS. 2A and 2B shows two optical images of composite adsorbent granules of Example 1 in different size ranges. FIG. 2A shows 10-20 mesh; FIG. 2B shows 20-40 mesh.

(3) FIGS. 3A and 3B graphically plots the adsorption performance evaluation breakthrough curves of the adsorbents in Example 5 and Comparative Example A.

DETAILED DESCRIPTION OF THE INVENTION

(4) It is understood that the terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. As used in this specification, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly indicates otherwise. The following terms in the Glossary as used in this application are to be defined as stated below and for these terms, the singular includes the plural.

(5) Various headings are present to aid the reader, but are not the exclusive location of all aspects of that referenced subject matter and are not to be construed as limiting the location of such discussion.

Glossary

(6) Ambient temperature means room temperature, usually from 20-25° C.

(7) wt % means percent by weight

Discussion

(8) The instant invention discloses a composition and a process for producing composite adsorbents comprised of zeolite and carbon having desired shapes and sizes for adsorption applications, made by mixing together components of a geopolymer material, a carbonaceous material, and an alkali activating agent, wherein the alkali activating agent to carbonaceous material solid mass ratio of at least 0.25:1, respectively, to produce a paste mixture having a uniform composition and desired rheology for shaping; processing the paste using common adsorbent shaping methods, including granulation or extrusion, to form granules or pellets to achieve suitable sizes for adsorption processes; chemically activating the carbonaceous material at a temperature generally higher than 400° C., preferably in the range of 400-1,000° C., in an inert gas, such as N.sub.2, using the alkali activating agent included in the composition to in-situ produce activated carbon; conducting hydrothermal treatment to convert part of the geopolymer to zeolite; washing and drying the produced zeolite and carbon composite adsorbents for adsorption applications. FIG. 1 illustrates these process steps as a flow diagram for manufacturing composite adsorbents of the instant invention.

(9) Geopolymers are a class of aluminum silicate inorganic polymers which have an amorphous 3-dimensional polysialate network consisting of SiO.sub.4 and AlO.sub.4 tetrahedra. The formation of a geopolymer involves an aluminosilicate source material and an alkali silicate activator solution. In a typical synthesis, calcined clay or fly ash is mixed with alkali silicate solutions to form a geopolymer. The geopolymerization process consists of three stages: 1) dissolution of aluminum and silicon ions from the aluminosilicate source to form mobile monomers through the reaction with hydroxide ions; 2) re-orientation and re-arrangement of the monomers and formation of larger oligomers; 3) polycondensation of oligomers to form rigid 3-dimensional network of oxygen bonded SiO.sub.4 and AlO.sub.4 tetrahedra.

(10) Geopolymer materials can set at ambient temperature and achieve many excellent material properties such as high strength as well as thermal and chemical stabilities. One typical characteristic of geopolymers is their ability to set and develop material strength at ambient or slightly elevated temperature after mixing. They have been used in a number of applications such as construction cement and refractory materials. Geopolymerization process starts as soon as an alkali silicate activator is mixed with an aluminosilicate source material. Geopolymers typically set in a few hours, during which the mixture develops rigid polymeric network, loses plasticity and becomes hard, and achieves high material strength.

(11) Activated carbon can be manufactured from carbonaceous materials, including coal, petroleum coke, biomass, and others. Due to abundant availability and low cost of biomass wastes, they have been increasingly used as the raw material for activated carbon production. Activated carbon can be produced by physical or chemical activation methods. The physical activation method is comprised of two main processes: carbonization and activation by steam or CO.sub.2. Chemical activation is a single step process conducted in the presence of activating agents such as alkali hydroxide, phosphoric acid, ZnCl.sub.2, etc. Chemical activation generally occurs at a lower temperature than physical activation (generally >800° C.). It has been reported that when an alkali hydroxide such as NaOH is used as the activating agent, high surface area activated carbons are produced.

(12) In the instant invention, it has now been found that mixing a geopolymer material, a carbonaceous material, and an alkali activating agent at an alkali activating agent to carbonaceous material solid mass ratio of at least 0.25:1, respectively, prepares a paste mixture with uniform composition and desired rheology, enables effective shaping of the paste mixture to form granules or pellets with desired shapes and sizes using common adsorbent shaping methods, such as granulation or extrusion, and allows development of sufficient material strength in a short time period through geopolymerization at ambient or slightly elevated temperature for further processing to produce composite adsorbents.

(13) After a geopolymer material is prepared and mixed with a carbonaceous material and an activating agent to produce a uniform paste, the geopolymerization process starts. As geopolymer materials generally take a few hours of time to cure and harden at ambient temperature, the paste mixture can be processed to granules using granulation methods or pellets using extrusion methods. After granules or pellets are formed, they can be kept at ambient temperature to cure or heated to an elevated temperature, which is generally lower than 150° C., to accelerate curing to develop sufficient material strength for further processing such as sieving, activation, and hydrothermal treatment.

(14) The instant invention has now shown that most carbonaceous materials, including coal, petroleum coke, biomass, and others commonly used to manufacture activated carbon can be processed to particle sizes smaller than that of granules or pellets and can produce and form well-mixed paste mixtures with geopolymer materials. Additionally, biomass materials can be pre-mixed with alkali activating agent solutions to age and optionally heated to soften and break down biomass materials for easy processing and improved uniformity. Furthermore, the pre-mixing and aging of biomass materials with alkali activating agent solutions also improve alkali activation of the biomass mass to produce activated carbon.

(15) For carbonaceous materials such as coal, charcoal, and other easy-to-grind materials, they can be conveniently ground to produce powders and form uniform paste mixtures with geopolymer materials. For paste like carbonaceous materials such as petroleum asphalt, they can be directly mixed with geopolymer materials to produce uniform mixtures. For biomass carbonaceous materials such as wood, they can processed to produce sawdust, pre-mixed with alkali activating agents such as NaOH solutions to break down the materials, or pyrolyzed to produce charcoal for easy grinding. The processing of carbonaceous materials to small particle sizes not only improve the uniformity of the composite composition but also enhance the alkali activation and hydrothermal treatment processes to produce activated carbon and zeolite in the composite adsorbents.

(16) It is advantageous to use alkali activating agents such as alkali hydroxides at an alkali activating agent to carbonaceous material solid mass ratio of at least 0.25:1, more preferable to be at least 0.5:1, and even more preferable to be at least 1:1 in the mixture composition to manufacture zeolite and carbon composite adsorbents. Alkali hydroxides such as NaOH not only act as the activation agent to chemically convert carbonaceous materials to activated carbon but also provide the necessary alkali components for the effective conversion of geopolymer to zeolite. In addition, adding alkali hydroxide activating agents helps the dissolution of aluminosilicate material in the geopolymer composition and improve the geopolymerization process.

(17) The alkali activating agent can be added as a part of the geopolymer material composition or in addition to the geopolymer material and carbonaceous material mixture. The alkali activation of carbonaceous materials in the mixture composition can be conducted in an inert gas such as nitrogen or others, at a temperature of higher than 400° C., generally between about 400 and about 1,000° C. It is also now found that alkali activation also facilitates the conversion of geopolymer to zeolite under hydrothermal conditions.

(18) After the alkali activation of the mixture composition, the activated granules or pellets can be hydrothermally treated to convert part of geopolymer to zeolite. Since geopolymer is an aluminum silicate material, depending on the composition, geopolymer can be partly converted to zeolite by hydrothermal treatment in water, an alkali solution, or other media. The zeolite hydrothermal synthesis normally comprises heating the geopolymer material to a temperature between about 30 and about 200° C. for a period of time between 1 and 168 hours to produce the desired zeolite. The type of zeolite formed after the hydrothermal treatment depends on the geopolymer composition and hydrothermal conditions and includes A, X, Y, T, P, β, mordenite, and other zeolites. After hydrothermal treatment, the in-situ produced zeolite and carbon composite adsorbents are washed and dried for adsorption applications.

(19) The instant invention provides a unique mixture composition and advantageous manufacturing process to produce high performance and low cost zeolite and carbon composite adsorbents with desired shapes and sizes. Instead of using expensive zeolite and activated carbon as the raw materials to produce zeolite-carbon composite adsorbents, low cost and abundant geopolymer materials and carbonaceous materials such as biomass are used to prepare mixture compositions for composite adsorbent fabrication. The mixture compositions can be easily shaped using common shaping methods to produce granules or pellets with suitable sizes and good strength. The use of alkali activating agents in the mixture composition not only enables geopolymerization to provide good material strength but allows chemical activation of carbonaceous materials to activated carbon and facilitates effective conversion of geopolymer to zeolite to form zeolite-carbon composite adsorbents.

(20) This process can be further understood by referring to the flow diagram of FIG. 1 as discussed below:

(21) Geopolymer materials according to Step 1 of FIG. 1 can be prepared by mixing an aluminosilicate source material, an alkali activator material, and a carrier fluid. The general formula of geopolymers is M.sub.n[—(SiO2).sub.z—(AlO2)-].sub.n, where M is a monovalent cation, z is the ratio of Si to Al, and n is the degree of polymerization. M is typically an alkali metal such as lithium, sodium, potassium, or other monovalent cation and z is typically 1, 2, 3, or up to 32. The geopolymer materials can be prepared using any suitable composition defined by the general formula of a geopolymer.

(22) The geopolymer composition according to Step 1 of FIG. 1 generally includes an aluminosilicate source. Exemplary aluminosilicate materials include, but are not limited to metakaolin, calcined kaolin clays, fly ash, blast furnace slags, aluminum-containing silica fume, and others. It is preferred that the aluminosilicate source is metakaolin, calcined clays, fly ash, slags, or a combination of two or more of these materials.

(23) The geopolymer composition according to Step 1 of FIG. 1 generally includes an alkali silicate activator. The alkali silicate activator generally comprises an alkali metal or alkaline earth metal silicate component. References herein to “alkali” compounds are intended to refer to alkali metals (e.g., Li, Na, and K) and alkaline earth metal (e.g., Mg, Ca) compounds. The alkali silicate component comprises at least one of sodium silicate, potassium silicate, lithium silicate, calcium silicate or magnesium silicate. The alkali silicate component preferably comprises sodium silicate.

(24) The geopolymer composition according to Step 1 of FIG. 1 generally includes a carrier fluid. The carrier fluid can be water, organic solvents, other liquids, or a combination of two or more fluids. It is preferred that the carrier fluid is water. If the aluminosilicate source or metal hydroxide activator is already in a liquid state, it is considered that the geopolymer composition already has a carrier fluid present.

(25) The carbonaceous materials according to Step 1 of FIG. 1 are materials that contain a large carbon content. Examples of carbonaceous materials include coal, petroleum coke, asphalt, wood, bamboo, coconut husk, lignite, rice husk, waste rubber tire, and others. Depending on the nature of carbonaceous materials, they can be used directly to mix with geopolymer materials, ground or pyrolyzed before grinding to obtain a powder form, or pre-treated with chemicals such as alkali hydroxide to break down the materials for easy processing.

(26) The alkali activating agents according to Step 1 of FIG. 1 generally includes an alkali metal or alkaline earth metal hydroxide or salt commonly used for chemical activation to produce activated carbon. The alkali hydroxide component comprises at least one of sodium hydroxide, potassium hydroxide, lithium hydroxide and the like, preferably sodium hydroxide. The alkali activating agent to carbonaceous material solid mass ratio in the mixture composition is preferably at least 0.25:1, more preferably at least 0.5:1, and even more preferably at least 1:1. The alkali activating agents can be added as a part of the geopolymer material composition or in addition to the geopolymer material and carbonaceous material mixture.

(27) The adsorbent shaping method according to Step 2 of FIG. 1 include granulation, extrusion, and other adsorbent manufacturing methods. Adsorbent granulation methods such as wet granulation, dry granulation, spray drying, and others are commonly used to produce adsorbent granules. Extrusion methods are generally used to produce adsorbent pellets in cylindrical or other shapes.

(28) The curing of the composition according to Step 3 of FIG. 1 can be conducted at ambient temperature or by raising the temperature of the mixture composition by providing a heat source. The heating can be achieved by convection, radiation, or conduction methods. The curing can be carried out at a temperature between about 20 and about 150° C., preferably between about 40 and about 100° C., more preferably between about 50 and about 80° C. The curing of the geopolymer composition may be conducted generally between 1 and 72 hours, preferably between about 4 to about 48 hours, and more preferably between about 8 to about 24 hours. The curing of the mixture composition may be carried out in presence of air, moisture, steam, flue gas, water, solvents, or other gases or liquids. Most preferably the curing is carried out in the presence of moisture, water, or steam.

(29) The alkali activation of carbonaceous materials in the mixture composition according to Step 4 of FIG. 1 can be conducted in inert gases such as nitrogen, argon, helium or others in the presence of an alkali activating agent at a temperature generally between about 400 and about 1,000° C., preferably between about 500 and about 900° C., and more preferably between about 600 and about 800° C. to produce activated carbon. Optional treatment in CO.sub.2, steam, or other gases may be conducted to further improve the properties of the activated carbon.

(30) The hydrothermal treatment of an activated mixture composition according to Step 5 of FIG. 1 is carried out by heating in a hydrothermal treatment medium at a temperature necessary to convert at least part of the geopolymer into a zeolite. Depending on the type of geopolymer composition and desired zeolite type, the hydrothermal treatment is generally performed at a temperature below about 250° C., advantageously below about 200° C., preferably below about 150° C. and within the range of about 40 to about 150° C., and most preferably within the range of about 60 to about 120° C. The hydrothermal treatment time is generally between 1 and 168 hours, preferably between 1 and 72 hours, more preferably between 2 to 48 hours, even more preferably between 4 to 24 hours.

(31) The invention will be further clarified by a consideration of the following examples, which are intended to be purely exemplary of the invention.

(32) Materials and Equipment:

(33) activated carbon adsorbents were purchased as Filtrasorb 300 from Calgon Carbon, Moon Township, Pa.

(34) h means hour

(35) L means liter

(36) metakaolin was purchased as PowerPozz metakaolin from Advanced Cement Technologies, Blaine, Wash.

(37) meq means milliequivalent

(38) ppm means parts per million

(39) sodium silicate solution was purchased as Grade 40 from Occidental Chemical Corporation, Dallas, Tex.

(40) sodium hydroxide was purchased as 50% caustic soda diaphragm from Occidental Chemical Corporation, Dallas, Tex.

(41) zeolite adsorbents were obtained as 13X zeolite beads from UOP, Des Plaines, Ill.

Example 1

(42) A composite mixture composition is prepared by mixing and aging wood sawdust with a sodium hydroxide activating agent solution at ambient temperature for overnight, mixing metakaolin with a sodium silicate activator solution to prepare a geopolymer composition, and then mixing the above two mixtures right after the geopolymer preparation to produce a uniform paste mixture. The composite mixture comprises by weight 22 wt % of metakaolin, 13 wt % of sodium silicate solution, 22 wt % of dry wood sawdust, and 43 wt % of sodium hydroxide activating agent solution. The alkali activating agent (sodium hydroxide solid) to carbonaceous material (wood sawdust) solid mass ratio is 1:1.

(43) The prepared composite paste mixture is ground in a coffee grinder and then tumbled in a rotating tumbler to shape the mixture and form green granules. The green granules are placed into a sealed container and heated at 60° C. to cure the geopolymer composition and further treat the wood material in the granules with alkali activating agent. The cured granules are transferred into a furnace and heated at 700° C. for 1 h in nitrogen to activate the wood material in the granules using the incorporated alkali hydroxide to produce activated carbon. The activated granules are subjected to hydrothermal treatment in a 1 mol/L sodium hydroxide solution at 75° C. for 24 h to form zeolite. After the hydrothermal treatment, the produced granules are washed with de-ionized water and dried at 120° C. for adsorption applications. FIG. 2 shows optical images of composite adsorbent granules in 10-20 (FIG. 2A) and 20-40 (FIG. 2B) mesh size ranges fabricated in this example.

(44) After drying, the composite granules are ground to powder and X-ray diffraction (XRD) is conducted to characterize the crystal phases of the material. Zeolites NaX and NaA are present in the composite material with NaX as the major phase, indicating zeolites are formed from geopolymer after hydrothermal treatment.

(45) For inorganic adsorption performance evaluation, 0.1 g of 20-40 mesh size composite granules are added into 100 mL of 200 ppm of copper sulfate solution and shaken at 100 rpm for 24 h. The copper solution is filtered after the test and its Cu.sup.2+ concentration is analyzed using a photometer system. The composite adsorbents have a Cu.sup.2+ adsorption capacity of 39 meq per 100 g (meq/100 g), higher than those of commercial zeolite granules (28 meq/100 g for 13X zeolite beads from UOP, Des Plaines, Ill.) and activated carbon granules (14 meq/100 g for Filtrasorb 300 from Calgon Carbon, Moon Township, Pa.).

(46) For organic adsorption performance evaluation, 0.1 g of 20-40 mesh size composite granules are added into a 500 ppm phenol solution and shaken at 100 rpm for 24 h. The phenol concentration of the filtrate is analyzed using a gas chromatography. The composite adsorbents have a phenol adsorption capacity of 59 mg/g, higher than that of commercial zeolite granules (5 mg/g for 13X zeolite beads from UOP, Des Plaines, Ill.) but lower than that of commercial activated carbon granules (189 mg/g for Filtrasorb 300 from Calgon Carbon, Moon Township, Pa.).

Example 2

(47) A composite mixture composition is prepared by mixing and aging wood sawdust with a sodium hydroxide activating agent solution at 60° C. for overnight, mixing metakaolin with a sodium silicate activator solution to prepare a geopolymer composition, and then mixing the above two mixtures right after the geopolymer preparation to produce a uniform paste mixture. The composite mixture comprises by weight 15 wt % of metakaolin, 9 wt % of sodium silicate solution, 22 wt % of dry wood sawdust, and 54 wt % of sodium hydroxide activating agent solution. The alkali activating agent (sodium hydroxide solid) to carbonaceous material (wood sawdust) solid mass ratio is 1.2:1.

(48) The prepared composite paste mixture is processed using the same shaping, alkali activation, and hydrothermal process as that in Example 1. XRD analysis of the fabricated composite adsorbents shows that zeolites NaX and NaA are formed in the composite material with NaX as the major phase. The inorganic and organic adsorption performance of the composite adsorbents are subjected to the same adsorption tests as that in Example 1. The composite adsorbents have a Cu.sup.2+ adsorption capacity of 45 meq/100 g and a phenol adsorption capacity of 71 mg/g.

Example 3

(49) A composite mixture composition is prepared by mixing wood sawdust with a sodium hydroxide activating agent solution, mixing metakaolin with a sodium silicate activator solution to prepare a geopolymer composition, and then mixing the above two mixtures right after the geopolymer preparation to produce a uniform paste mixture. The composite mixture comprises by weight 27 wt % of metakaolin, 16 wt % of sodium silicate solution, 14 wt % of dry wood sawdust, and 43 wt % of sodium hydroxide activating agent solution. The alkali activating agent (sodium hydroxide solid) to carbonaceous material (wood sawdust) solid mass ratio is 1.5:1.

(50) The prepared composite paste mixture is processed using the same shaping, alkali activation, and hydrothermal process as that in Example 1. XRD analysis of the fabricated composite adsorbents shows that zeolites NaX and NaA are formed in the composite material with NaX as the major phase. The inorganic and organic adsorption performance of the composite adsorbents are subjected to the same adsorption tests as that in Example 1. The composite adsorbents have a Cu.sup.2+ adsorption capacity of 27 meq/100 g and a phenol adsorption capacity of 30 mg/g.

Example 4

(51) A composite mixture composition is prepared by mixing and aging wood sawdust and charcoal powder with a sodium hydroxide activating agent solution, mixing metakaolin with a sodium silicate activator solution to prepare a geopolymer composition, and then mixing the above two mixtures right after the geopolymer preparation to produce a uniform paste mixture. The composite mixture comprises by weight 13 wt % of metakaolin, 8 wt % of sodium silicate solution, 16 wt % of dry wood sawdust, 8% of wood charcoal powder, and 55 wt % of sodium hydroxide activating agent solution. The alkali activating agent (sodium hydroxide solid) to carbonaceous material (wood sawdust and charcoal powder) solid mass ratio is 1.1:1.

(52) The prepared composite paste mixture is processed using the same shaping, alkali activation, and hydrothermal process as that in Example 1. XRD analysis of the fabricated composite adsorbents shows that zeolites NaX and NaA are formed in the composite material. The inorganic and organic adsorption performance of the composite adsorbents are subjected to the same adsorption tests as that in Example 1. The composite adsorbents have a Cu.sup.2+ adsorption capacity of 37 meq/100 g and a phenol adsorption capacity of 79 mg/g.

Example 5

(53) A composite mixture composition is prepared by mixing metakaolin with a pre-mixed sodium silicate and sodium hydroxide activator solution to prepare a geopolymer composition, and then mixing the above geopolymer with wood sawdust to produce a uniform paste mixture. The composite mixture comprises by weight 18 wt % of metakaolin, 10 wt % of sodium silicate solution, 18 wt % of dry wood sawdust, and 54 wt % of sodium hydroxide activating agent solution.

(54) The prepared composite paste mixture is processed using the same shaping, alkali activation, and hydrothermal process as that in Example 1, except that the alkali activation temperature is 750° C. XRD analysis of the fabricated composite adsorbents shows that zeolites NaX and sodalite are formed. The composite adsorbents are calcined in air at 850° C. to determine their carbon content, which is about 20 wt %. For inorganic and organic adsorption performance evaluation, 2.5 g of 20-40 mesh size composite granules are used to conduct fixed bed breakthrough curve analysis. A test column with 1 cm inner diameter is used. An influent solution with 400 ppm of Cu.sup.2+ and 1000 ppm of phenol is used with a flow rate of 1 mL/min. Effluent samples are analyzed to determine the effluent pollutant concentration at a given time (C.sub.t). Breakthrough curves are plotted using the ratio of effluent pollutant concentration (C.sub.t) over influent pollutant concentration (C.sub.0) with respect to time.

(55) Breakthrough curves for the adsorption of Cu.sup.2+ and phenol on the composite adsorbents in this example is shown in FIG. 3. Breakthrough curves for the adsorption of Cu.sup.2+ on the composite adsorbents (FIG. 3A) indicates that the composite adsorbents are more effective in removing inorganic pollutants and also have a greater adsorption capacity than a hybrid activated carbon and zeolite adsorbents in Comparative Example A. Breakthrough curves for the adsorption of phenol on the composite adsorbents (FIG. 3B) implies that the composite adsorbents have organic adsorption effectiveness and capacity close to those of the hybrid activated carbon and zeolite adsorbent systems in Comparative Example A.

Comparative Example A

(56) For the treatment of complex wastewater containing both inorganic and organic pollutants, to improve pollutant adsorption performance, hybrid adsorbent systems consisting of zeolite and activated carbon in series are used in industrial applications. Since there are about 20% by weight of carbon in the composite adsorbents in Example 5, to compare fixed bed adsorption performance of the composite adsorbents against the hybrid adsorbent systems, a hybrid adsorbent system containing 20 wt % of activated carbon adsorbents followed by 80 wt % of zeolite adsorbents are used. In each test, 2.5 g of hybrid adsorbents are used and the test conditions are the same as those used as in Example 5. Breakthrough curves for the adsorption of Cu.sup.2+ and phenol on the hybrid adsorbents in this example are shown in FIG. 3A and FIG. 3B.

Comparative Example B

(57) To evaluate the feasibility of using a mixture composition comprised of a geopolymer material, a carbonaceous material, and an ex-situ produced, pre-synthesized zeolite material to in-situ produced activated carbon by alkali activation at high temperatures and fabricate zeolite and activated carbon composite adsorbents, a commercial zeolite powder is employed to replace a portion (up to 20%) of the metakaolin material used in Example 5 while keeping other material components the same to prepare a composite paste mixture containing pre-synthesized zeolite material. The zeolite containing composite paste mixture is processed using the same shaping, curing, and alkali activation process.

(58) XRD analysis of the cured composite mixture shows that zeolites NaX is present in the mixture along with amorphous geopolymer material, indicating that zeolite NaX has been incorporated in the mixture. However, after alkali activation of the cured mixture at 750° C. in nitrogen to activate the wood material in the mixture to produce activated carbon, XRD analysis of the activated composite mixture shows that the zeolite phase is no longer present in the mixture, suggesting that the incorporated zeolite NaX has been destroyed by the carbon alkali activation process. Therefore, using a mixture composition comprised of a geopolymer material, a carbonaceous material, and an ex-situ produced, pre-synthesized zeolite material to in-situ produce activated carbon by alkali activation at high temperatures will not lead to the formation of zeolite and activated carbon composite adsorbents.

(59) Although the invention has been described with reference to its preferred embodiments, those of ordinary skill in the art may, upon reading and understanding this disclosure, appreciate changes and modifications which may be made which do not depart from the scope and spirit of the invention as described above or claimed hereafter. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the general manner of carrying out the invention.