Patent Application
20240384042
The invention relates to polyvinyl alcohol (PVA) containing gel and gel beads that optionally may contain polyurethane (PU), methods for making gel and gel beads, methods for immobilizing substances such as microorganisms, cells, enzymes, and/or other materials in gel and gel beads, and methods for using such gel and gel beads in applications.
The use of immobilized microorganisms and enzymes has been considered as an alternative technology for wastewater treatment to replace conventional suspension sludge (SS) systems, such as an activated sludge system (Dumitriu and Chornet, 1998). Entrapment of microorganisms and enzymes in polymeric gel has been done previously but with various disadvantages (Kuraray Co., Ltd., 2012; Aslam et al., 2018). For example, there have been many drawbacks to using PVA for immobilization, such as a resulting weak physical structure and significant adhesion problems. The leakage of PVA gel from the surface of beads often occurred under mechanical agitation from water flow or aeration. A significant PVA biological decomposition problem was caused by entrapped microorganisms such as denitrifiers, e.g., Pseudomonas, etc. Such disadvantages rendered the lifetime of the PVA gel beads to a limited useful period (e.g., a few months for some applications).
Some modifications of PVA gel beads involved a modification of the chemical structure of PVA gel beads using acetalization (Kuraray Co., Ltd., 2012), etherification (Schmidt et al., 1934) or other modifications (Aslam et al., 2018). Although this functional group modification might make PVA gel beads stronger to resist microbial decomposition, there are several drawbacks of these attempts, including that (1) they are not cost effective and require significant amounts of energy, (2) they may use aldehydes, especially glutaraldehyde, which are toxic to microorganisms, (3) common microorganisms cannot survive under certain process conditions that were applied, for example at pH<3 and temperatures of 40°-80° C., (4) the weak physical structure produced causes compaction in filters, and (5) the formation of gel beads still relies on alginate, etc., in a calcium ion solution. The structure of alginate is easily disintegrated into pieces because the calcium ion in the center of chelates can be withdrawn and replaced by phosphates in, for example, natural water. Also, alginate itself is easily decomposed by microorganisms as a carbon source.
Some previous reports suggested environmentally friendly modifications of the immobilization process using a particular PVA-boric acid method. Hwang suggested in U.S. provisional 62/856,328 (Jun. 3, 2019) that adding sodium chloride, calcium chloride and magnesium sulfate at the end of the immobilization process would improve the surface strength and solve the adhesion problem. However, it did not prevent the significant leakage of PVA gel from inside of gel beads or the end of the tadpole-shape gel beads, indicating that the major reason for the adhesion problem was still present and not solved. Hwang et al. described in a utility patent in 2014 (R.O.C. patent No. I425050) a development of ether-type anionic polyurethane (PU) gel beads. No PVA was described in those gel beads in the 2014 application. Earlier, Hwang et al. (https://www.slideserve.com/tiara/pu-pva) in 2005 disclosed PU/PVA immobilization cell beads. There is very little discussion about the PU/PVA immobilization cell beads and the PU gel beads, because of the very weak physical structure that resulted, which is not suitable for being used as a filter or for other purification or other processing methods.
U.S. Pat. No. 5,290,693 (1994) disclosed the hardening of PVA gel beads by adding phosphates. However, the gel beads disclosed there can still leak because using phosphate to harden the gel beads resulted in the gel beads not being hard enough.
An improved method for making improved gel and gel beads with immobilized substances (e.g., microorganisms such as bacteria and new substances not immobilized before) is thus needed. Such a method could be improved by using less harsh, more efficient and cost-effective processes and semi-continuous or continuous processes rather than discrete modes. The resulting characteristics of the gel and gel beads could also be improved by providing improved stability, improved viability of the immobilized substance, less leakage, improved hardness, and reinforcement.
The embodiments of this invention include PVA and/or PU/PVA gel and gel beads with improved structures and properties (e.g., stability, hardness, reinforcement, less harsh environments, less leakage) containing immobilized substances. The embodiments of this invention also include novel and non-obvious methods (e.g., continuous, efficient processes, such as with extruders) and apparatus for making PVA and/or PU/PVA gel and gel beads containing one or more immobilized substances such as microorganisms (e.g., bacteria, algae, fungi, protozoa, etc.), cells, enzymes and/or other materials (e.g., other chemicals such as non-enzymes, other living organisms, soil, sludge, mixtures of purified, partially purified or unpurified materials).
Embodiments of these gel, gel beads, methods and apparatus may comprise several operations that can be performed serially or combined. These operations include forming a PVA slurry solution, and, optionally, combining PU with PVA to form a PU/PVA slurry solution. The PU is preferably an ether-type hydrophilic polyurethane and it may be heated or unheated before use or in the slurry solution. We are using the phrase “slurry solution” to describe a slurry and/or solution that may be complex with several components or phases present at once or at different times (e.g., components and phases present such as a slurry, a powder, a mixture, a solution, a precipitate, etc.).
Embodiments of these gel, gel beads, methods and apparatus may also comprise combining one or more anions (e.g., anion releasing compounds) with the PVA and/or PU/PVA slurry solution and then forming PVA gel and/or PU/PVA gel. The one or more anions (e.g., from added anion releasing compounds) that are used can preferably comprise sulfate, phosphate, and/or borate anions, and other suitable anions or anion releasing chemicals, as will be apparent to the person of ordinary skill in the art. These operations can be done serially or in their various combinations.
Embodiments of these gel, gel beads, methods and apparatus may optionally comprise combining the PVA and/or PU/PVA slurry solution with an etherification compound. The etherification compound is one that increases or enhances (e.g., catalyzes) ether formation and is preferably sulfuric acid or another acid.
Embodiments of these gel, gel beads, methods and apparatus may comprise then combining one or more substances, such as microorganisms (e.g., bacteria, algae, fungi, protozoa, etc.), cells, enzymes and/or other materials (e.g., other chemicals such as non-enzymes, other living organisms, soil, sludge, mixtures of purified, partially purified or unpurified materials), with the slurry solution, and then combining boric acid solution with the slurry solution with the one or more substances to immobilize and forming gel or gel beads. These operations can be done serially or combined together. The environment of the slurry solution may be improved for a given application by avoiding potentially harsh conditions that may apply. Thus, the pH of the slurry solution for some applications (e.g., microorganisms, cells) may preferably be less than about pH 7, more preferably above about pH 3, and most preferably be above about pH 5.5. Other applications may benefit from different pH ranges.
Preferred substances to be immobilized are microorganisms, cells, enzymes, non-enzyme chemicals, sludge, or mixtures of materials.
Embodiments of these gel, gel beads, methods and apparatus may also comprise forming a bead or other shape for the gel with, for example, a discrete-mode dropping apparatus, such as the apparatus that is known in the art or, more preferably, extrusion apparatus. The operation of forming a bead or other shape for the gel with an extrusion apparatus is preferably done as part of a semi-continuous or continuous process. The operation of forming a gel is preferably done by spreading it on a surface or support, such as a board, plate or reaction component, for use in a process or method.
Embodiments of these gel, gel beads, methods and apparatus may then comprise combining one or more hardening agents with the gel or gel beads containing the one or more immobilized substances. The one or more hardening agents preferably comprises a cation or a cation releasing compound, such as an alkali metal, an alkaline earth metal, other metal ion, and/or a mixture thereof. The alkali metal preferably is Li+, Na+, K30 , and/or mixtures thereof. The alkaline metal is preferably Ca2+, Mg2+, and/or mixtures thereof. The other metal ion that can be used is preferably Al+3, Fe2+, Fe+3, Zn2+ and Cu2+, and/or mixtures thereof.
Embodiments of these gel, gel beads, methods and apparatus may then comprise, optionally, combining one or more reinforcement agents with the gel or gel beads containing the one or more immobilized substances. The optional one or more reinforcement agents preferably comprise fibers. Preferable fibers are synthetic fibers such as fibers of polyacrylic acid, polyvinyl acetate, polyacrylamide fibers and natural fibers such fibers from algae, cellulose, pulp, cotton, linen and other natural sources, and/or mixtures thereof. These operations set forth above can be done serially or in their various combinations.
Preferred embodiments of the gel beads of this invention are gel beads comprised of PVA gel and/or PU/PVA gel, including linked PVA units and/or linked PU/PVA units; gel beads with one or more immobilized substances such as microorganisms (e.g., bacteria, algae), cells, enzymes and/or other materials; gel beads of a preferred size from about 2 mm to about 6 mm, and more preferred from about 3 mm to about 5 mm, and most preferred of about 4 mm; and gel beads with less than about 10% PVA or immobilized substance leakage from the gel beads after one week of use in an application such as an aqueous solution treatment process, and more preferred with less than about 1% PVA or immobilized substance leakage from the gel beads after one week of use in an application such as an aqueous solution treatment process, and most preferred with less than about 0.1% PVA or immobilized substance leakage from the gel beads after one week of use in an application such as an aqueous solution treatment process.
In certain preferred embodiments, including those in the paragraph above, gel beads have a hardness greater than or equal to about 0.03 kg/cm2, and more preferably, gel beads have a hardness greater than or equal to about 0.1 kg/cm2, and most preferably, gel beads have a hardness greater than or equal to about 0.5 kg/cm2. A hardness greater than or equal to about 0.03 kg/cm2 may improve processability in some embodiments of this invention.
In certain preferred embodiments, including those in the two paragraphs above, gel beads pass a stress test by showing preferably less than about 5% to about 10% leakage or loss of PVA or immobilized substance, more preferably less than about 1% leakage or loss of PVA or immobilized substance, and most preferably no measurable leakage or loss of PVA or immobilized substance. One such stress test uses a velocity gradient (G≥300 s−1) produced by strong agitation from coarse air bubbles for one week. Additional stress tests can be applied that mimic or relate to the given application in which the gel beads will be used to measure the leakage or loss of PVA from the beads for a relevant period of time. The leakage and loss of PVA from gel beads can be measured by, for example, measuring PVA in the solution, observation of a solution of the gel beads, observation of foaming, or measuring COD (chemical oxygen demand), for example, in a solution of reverse osmosis purified water.
Applications for the embodiments of this invention include using the PVA and/or PU/PVA gel or gel beads in various substrate and aqueous solution treatment, purification processes and manufacturing processes, as examples. These applications can comprise applying or otherwise combining the gel or gel beads of this invention that contain immobilized substances such as microorganisms (e.g., bacteria, algae, fungi, protozoa, etc.), cells, enzymes and/or other materials (e.g., other chemicals such as non-enzymes, other living organisms, soil, mixtures of purified, partially purified or unpurified materials) with substrates and aqueous solutions to, among other things, for example, reduce the COD (chemical oxygen demand), reduce volatile organic chemicals, reduce the odor, denitrify, nitrify, and/or purify the aqueous solution or produce products. The person of ordinary skill in the art understands how this application and combining of the gel and gel beads of this invention to these substrates and aqueous solutions can be done in, for example, in situ or in reaction tanks, reaction plates, reaction columns, other reaction vehicles (e.g., containers, tubes), and processes and/or be incorporated into pre-existing manufacturing and purification type processes and apparatus. Thus, this method may comprise applying the gel or gel beads containing the immobilized substances to a substrate, gas or aqueous solution, treating the substrate, gas or aqueous solution with the gel or gel beads, and recovering (e.g., retrieving, reclaiming, reusing, separating, filtering, removing, bypassing, etc.) the gel or gel beads from the treated substrate or aqueous solution. These applications can apply to many different types of substrates and aqueous solution treatments, including wastewater treatment, aquaculture water treatment, aquarium water treatment, chemical process solution treatment or production, manufacturing process solution treatment or production, biofuel and biodiesel production, antibiotic process solution treatment or production, and/or other pharmaceutical process solution treatment or production. Other applications of immobilized substances, including immobilized bacteria and algae, can be used with embodiments of this invention that are known, or will be known, to a person of ordinary skill in the art (e.g., components of devices, biosensors, bioreactors, environmental mitigation and remediation (e.g., metals, gases, toxins) applications).
Advantages of the embodiments of this invention are described and apparent throughout this specification. For example, certain embodiments permit the use of semi-continuous and/or continuous processing using an extruder, which has not been applied to relevant aqueous solutions or such gel beads in particular. The disclosed pre- and post-treatment modifications of PVA-boric acid immobilization processes for substances can provide more advantageous solutions, more stability, better strength, improved adhesion properties, less leakage, better physical and chemical structure, be more environmentally friendly, be more economical, etc., compared to previous applications of gel and gel beads, such as applications concerning wastewater treatment, and new applications that were not done before because of the drawbacks of the gel and gel beads used.
The invention provides a method of production of immobilized substances such as microorganisms (e.g., bacteria, algae, fungi, protozoa, etc.), cells, enzymes and/or other materials (e.g., other chemicals such as non-enzymes, other living organisms, soil, sludge, mixtures of purified, partially purified or unpurified materials) in gel and gel beads using PVA and/or PU/PVA for application in many different processes involving substrates and/or aqueous solutions, such as aquarium, aquaculture, water and wastewater treatment, and in manufacturing processes and production (e.g., the biochemical, chemical and pharmaceutical industry). In particular, it can increase the surface strength of gel and gel beads and reinforce the interior structure of the gel and gel beads through pre- and post-treatments combined with PVA-boric acid cell immobilization processes. At the same time, the invention can solve the significant adhesion problems of gel and gel beads. Thus, preferred embodiments of the gel and gel beads can maintain their dispersion during processes, conveyance and/or filtering through unit operations in manufacturing factories and treatment applications and their usage in different fields.
The invention also describes methods for improved throughput and/or mass production of immobilized substances in gel and gel beads. In particular, the use of high-productivity extruders, which have not been used with aqueous solutions at room temperature (Prüße et al., 2002), is now applied to the invention's production of immobilized substances in gel beads with the advantage of continuous discharge of PVA slurry solution in the method. Otherwise, other techniques, such as a dropping technique of manufacture using dropping apparatus, can only operate in a discrete mode.
Examples of methods of producing immobilized substances of this invention, comprises:
Embodiments of this invention can also use etherification as an alternative, for example, using ether-modified PVA as a matrix with/without other interior reinforcement materials mixed together to entrap substances such as microorganisms or enzymes into PVA gel ether-beads. A PVA of about 1% to about 20% can be modified by adding from about 0.01 to about 1% w/v sulfuric acid or another acid, an etherification compound. Also, PU can be added (e.g., from about 0.1 to about 20% PU) before or after PVA dissolution at about 90° to about 120° C. These embodiments of this invention can use significantly smaller amounts of PU (less than 5%) than what was previously used. It is surprising that such small amounts of PU can stabilize and prevent the leakage of PVA gel from gel beads. The alternative of using sulfuric acid or another acid for etherification of PVA can also prevent the leakage of PVA gel from the beads.
Thus, this invention provides an optional etherification modification that can prevent the leakage of PVA gel in PVA gel beads. Mechanical strength can further be improved by adding reinforcement materials. Some reinforcement materials such as synthetic fibers (e.g., PVAc (polyvinyl acetate), PAA (polyacrylic acid), and PAM (polyacrylamide), etc.) and/or mixtures thereof, and natural fibers (e.g., algae, cellulose, pulp, cotton, and linen, etc., and/or mixtures thereof) can be added alone or in combination to further increase mechanical strength.
The esterification of this invention can be modified by adding anions to PVA or PU/PVA gel to increase the mechanical strength of PVA or PU/PVA immobilized-substance gel beads. The anions include phosphates, sulfates and boric acid/borates at concentrations between about 0.01% to about 5%.
In pretreatment, the heating time of the PVA slurry solution is preferably about 30 to about 90 minutes (more preferably about 60 minutes). Thus, for example, with this pretreatment, preferably no leakage of PVA oligomers occurs from the gel or gel beads while the gel or gel beads undergo stress testing at the end of the process using coarse air bubble aeration or a similar technique of stress testing for about a week or more. A preferred stress test used was performed by preparing a 1-liter clean air sparger; adding 100 ml of the gel beads to the sparger; filling the air sparger with reverse osmosis (RO) water to 1 liter; agitating the air sparger; setting the airflow at 1000 ml/min (so the velocity gradient G can be about or greater than 300 sec−1); observing the accumulated bubble height and recording each day for one week. Bubble or foam height less than 5 cm is preferred. A more preferred stress test is to measure COD for leakage or loss of PVA. Useful testing and analysis of G is reported in “Coagulation and Flocculation in Water and Wastewater Treatment,” IWA Publishing, London, Seattle, Bratby J. (2006); reproduced in part at https://www.iwapublishing.com/news/coagulation-and-flocculation-water-and-wastewater-treatment.
In the post-treatment, after PVA and/or PU/PVA immobilized-substance gel and gel beads have been formed and removed from the boric acid solution, the gel and gel beads may be further hardened in a solution of alkali group or alkaline earth group metal salts that have concentrations of about 0.5 to about 25% for a period of time ranging between about 30 minutes to about 15 hours, preferably between about 1 to about 5 hours. Those hardening metals include Li+, Na+, K+, Ca2+, Mg2+. Other metal ions such as Al+3, Fe2+, Fe+3, Zn2+ and Cu2+ can also be used. A pH of about 4 to about 9 is preferred for the process.
In one embodiment of the invention, all of the aforementioned features are done to produce the gel or gel beads. In other embodiments of the invention, only one or more of the aforementioned features are done to produce the gel or gel beads. This flexibility is provided to improve the characteristics of the gel or gel beads overall for a given application, as some modifications may produce other weaknesses. In these embodiments, the intent is for the methods and steps to be applied to integrated solutions to achieve the maximum or optimum beneficial effects with the minimal weaknesses for the given applications.
Examples of the manufacturing equipment for gel and gel beads containing immobilized substances such as microorganisms and enzyme provided by the present invention includes a heating dissolution tank, a mixing tank, a conveying mechanism and a bead-forming tank. The heating dissolution tank contains PVA (or PU/PVA) particles, water and anions after heating to form a PVA (or PU/PVA) gel; the mixing tank contains PVA (or PU/PVA) gel mixed with substances such as microorganisms or enzymes. The conveying mechanism has a pipeline, an extrusion piece, a cutting piece and a porous cover. The pipeline has an outlet open and an inlet connected to the mixing tank. The extrusion piece is arranged in the pipeline and close to the outlet, the porous cover closes the outlet and has a plurality of openings, and the cutting piece is arranged outside the porous cover. The bead-forming tank connected to the outlet of the first pipeline fills the boric acid solution. The PVA (or PU/PVA) slurry solution is formed into a PVA (or PU/PVA) gel in the heating dissolution tank, and then mixed with one or more substances (such as microorganisms or enzymes) in the mixing tank, and then is conveyed to the bead-forming tank through the pipeline. The PVA (or PU/PVA) gel coming to the outlet of pipeline is continuously extruded from the opening of the porous cover, and the cutting piece is used for cutting the PVA (or PU/PVA) gel extruded from the opening into multiple pieces which then enter into the bead-forming tank filled with boric acid aqueous solution. The PVA (or PU/PVA) gel is then converted into a plurality gel beads containing immobilized substances in the boric acid aqueous solution of the bead-forming tank. If extrusion is not used, a dropping technique and apparatus can be applied to the gel to form the gel beads.
In certain preferred embodiments, for mass production using an extruder, the proposed modified PVA (or PU/PVA) gel is preferred to be pretreated to increase its viscosity to more than about 5000 CPS (preferably about 10000 CPS), which may be a minimum requirement for normal extruder operation of certain extruders.
The PVA or PU/PVA gel and gel beads containing immobilized substances can have a variety of uses and applications. For example, wastewater treatment, waste gas treatment, odor treatment, aquarium water treatment, aquaculture water treatment, manufacturing process solution treatment, chemical process solution treatment and production, substrate purification, pharmaceutical (drugs (e.g., antibiotics), supplements, ingredients) production, biofuel and biodiesel production and biochemical (e.g., enzymes, antibodies) production, among others.
The PVA or PU/PVA gel and gel beads containing immobilized substances can also improve the efficacy of current existing methods and processes. There is no leakage or reduced or minimal leakage of the PVA or PU/PVA gel and gel beads, an improvement of currently existing immobilized gel and gel beads. The no or reduced leakage of PVA or PU/PVA are from gel and gel beads of this invention that contain nanopores that can be entered and exited. For example, in an overgrowth algae environment in a pond, lake, reservoir, or river, the ammonia, nitrite and nitrate (NH4—N, NO2−—N, NO3−—N) in the water can enter the gel and gel beads and be converted to nitrogen gas off the water by the bacteria within. Ammonia and nitrite can be converted to nitrate which can then be absorbed together with phosphorous by water plants or algae to denitrify the water. The algae, having lost its nitrogen and phosphorous source, will then gradually be reduced and the overgrowth problem resolved or reduced. The water will then return to more environmentally acceptable conditions. Another example is in wastewater treatment, organic compounds (COD) can be converted to CO2, and nitrogen containing compounds and ammonia (NH4) can be converted to nitrate (NO3−) then to N2 through two different kinds (aerobics or facultative anaerobe) of bacteria in the gel and gel beads to achieve efficiency of wastewater treatment in a processing plant or factory.
In pretreatment embodiments of this invention, the outer surface and/or interior structure characteristics of the gel and gel beads are characteristics that may be improved. For example, PVA-boric acid methods can poison microorganisms and/or deactivate enzymes over time. Embodiments of this invention, because of the less harsh immobilization process, can lead to expanded applications to the immobilization of different substances that could not have been done before. It is also hypothesized that the leakage of PVA using such PVA-boric acid methods is due to the weak spots on the outer surface of PVA gel beads. Thus, pre-polymerization using anions for esterification of PVA oligomer to increase the strength of interior structure is an optional and preferred embodiment. Some chemical reactions such as etherification of PVA by sulfuric acid at about 120° C. or copolymer with ether-type PU heated or unheated also can be used to seal the bead tadpole end using a dropping technique or both side cutting sections using an extruder.
During gel formation of embodiments of this invention, there are several ways to increase the viscosity of the gel (e.g., PVA gel) that may be important for successful application of higher throughput and/or mass production processes using an extruder that can be operated in a semi-continuous or continuous mode, in contrast to a discrete-mode dropping technique.
In post-treatment embodiments of this invention, cations may be added to reinforce and improve the surface characteristics of the gel and gel beads that were, for example, treated by phosphates. These cations may aid the stability of and/or otherwise improve the surface of gel and gel beads (e.g., PVA gel beads), by, for example, having increased sealing and/or increased hardness. Once the surface properties are more stable and/or otherwise improved, the adhesion problem that may apply to such gel and gel beads may be reduced or eliminated.
The subject matter of this disclosure is now described with reference to the following Examples. These Examples are provided for the purpose of illustration only, and the subject matter is not limited to these Examples, but rather encompasses all variations which are evident as a result of the teaching provided herein.
A PVA-boric acid method that can use a dropping technique and apparatus or extrusion technique and apparatus and that can be combined with the pretreatment 20 and post-treatment 4050 embodiments of this invention is described herein as in
The conveying mechanism 120 has a pipeline 121, an extrusion piece 122, a cutting piece 123, and a porous cover 124. The pipeline 121 has an outlet 125 and an inlet 126 connected to the heating dissolution tank 110 and mixing tank 111. The extrusion piece 122 is placed in the pipeline 121 and can be driven to move closer to the outlet 125. The porous cover 124 closes the outlet 125 and has a plurality of openings 127, and the cutting piece 123 is placed outside the porous cover 124.
In this embodiment, the pipeline 121 may be, for example, L-shaped, and the conveying mechanism 120 includes a buffer chamber 128 connected to the pipeline 121 and used to receive the extrusion piece 122. The buffer chamber 128 is provided with a power device 1281 and a plunger rod 1282 connected between the power device 1281 and the extrusion piece 122. The extrusion piece 122 can be a plate corresponding to the diameter of the pipeline 121. When a certain volume of PVA and/or PU/PVA gel accumulates in the pipeline 121, the extrusion piece 122 can be driven by the power device 1281 into the pipeline 121 to push the PVA and/or PU/PVA gel out of the porous cover 124 from the pipeline 121. After the squeezing operation is completed, the extrusion piece 122 can return to the buffer chamber 128. However, the present invention is not limited to this. The pipeline 121 is not limited to the L-shape, and the extrusion piece 122 may also be placed in the pipeline 121 in other ways.
In this embodiment, there may be a plurality of cutting pieces 123, and each cutting piece 123 includes a rotating shaft 1230 and a plurality of blades 1231 connected to the rotating shaft 1230. When the rotating shaft 1230 of each cutting piece 123 rotates, the blade 1230 can slide through the opening 127 of the porous cover 124 to cut the PVA and/or PU/PVA gel extruded from the opening 127 into multiple sections. The transmission shaft 1230 may be connected to a motor (not shown) and a controller (not shown) such as a microcomputer in cooperation with the action of the extrusion piece 122. However, the present invention is not limited to this, and the cutting piece 123 may also be in other forms.
The bead-forming tank 130 is connected to the outlet of the pipeline 121 in this embodiment. As can be seen from the foregoing, the bead-forming tank 130 is suitable for filling a boric acid aqueous solution. The multi-sections PVA and/or PU/PVA gel can be formed into a plurality of gel beads containing immobilized substances in the boric acid aqueous solution of the bead-forming tank 130.
In this embodiment, the manufacturing apparatus 100 for gel beads containing immobilized microorganisms or enzyme (or other substances) includes a bead-hardening tank 140 placed beside the bead-forming tank 130 and connected with the bead-forming tank 130. The bead-hardening tank 140 is adapted to receive gel beads containing immobilized substances from the bead-forming tank 130. The bead-hardening tank 140 contains the aforementioned hardening solution, and the gel beads containing the immobilized substances can be dispersed with each other and hardened in the hardening solution. Gel beads with immobilized microorganisms, enzymes or other substances need to be separated from the boric acid aqueous solution before being placed in the bead-hardening tank 140, and a sieve apparatus (not shown) is used to separate the boric acid aqueous solution from the gel beads containing immobilized microorganisms or enzymes (or other substances) and recover them. A liquid discharging device (not shown) can be arranged in the sieve apparatus for recovery of boric acid aqueous solution back to bead-forming tank 130.
In this embodiment, the apparatus 100 for immobilizing microbial gel bead particles includes a culture medium tank 150 placed beside the bead-hardening tank 140. The culture medium tank 150 is adapted to receive gel beads containing immobilized microorganisms, enzymes or other substances from the bead-hardening tank 140 and contains the culture medium. Certain of the immobilized substances that can be used, such as microorganisms immobilized in the gel beads, can be further cultivated in the culture medium tank 150. The gel beads containing immobilized microorganisms, enzymes or other substances can be stored in the culture medium tank 150 before sale.
The demonstration of an embodiment of the present invention was performed at a local machinery development factory. We first added anions (NaH2PO4, Na2HPO4, MgSO4, and H2SO4, respectively) and PU to a PVA slurry solution to increase the viscosity (as seen in Table 1) to form a PU/PVA gel, and the PU/PVA gel was quickly formed into immobilized microorganisms or enzyme gel beads in the bead-forming solution containing 7% of boric acid and phosphates. Then, the immobilized microorganisms or enzyme gel beads formed in the bead-forming solution were placed into the many different bead-hardening solutions that were composed of 1% of sodium chloride, ammonium chloride, ammonium sulfate or sulfuric acid, respectively. After the immobilized microorganisms or enzyme gel beads are soaked in the bead-hardening solution for a period of time (5 hours), the beads were hardened, and the adhesion of beads did not appear.
#1measured after two weeks;
#2when the trace amount of FeO was added.
Results in Table 1 show that the extruder can perform well when the PVA or PU/PVA gel have a viscosity of more than about 1810 CPS. Some factors affecting viscosity are PU and PVA concentration, disodium hydrogen phosphate concentration, the gel stored time, the degree of saponification, etc. Lot No. 13-14 could form small gel beads with size smaller than 1 mm that is too small for practical use in some wastewater treatment applications. One can make these small beads into fibers to be used in the pre-coated filters for treatment of aquarium water. One can use a double screw extruder for more viscous gel to make larger beads. Lot No. 23 successfully formed larger beads as shown in Table 2 which can be used directly in the wastewater treatment.
Results in Table 2 show the PVA gel containing immobilized substances in different hardening solution at a concentration of 1%. The cylinder shape of gel beads turned into spherical shapes after the gel beads were swollen in water. Adding sulfuric acid (Lot No. 52) on the surface of PVA gel beads can prevent the adhesion problem and make gel beads disperse well. It was determined that for this embodiment, chloride made bead surfaces whiter. The sulfate will make gel beads more translucent as compared to certain other hardening solutions. The “whiter” means the surface of PVA gel beads is more condensed than “translucent” is some embodiments. All of the hardening agents that show positive improvement are embodiments of qualified hardening solutions for this example. Lot 51 gel beads have a hardness at 0.037kg/cm2 and size at 4.50±0.383 mm.
In this example, the appearance is shown of embodiments of the PVA gel beads where the 1% sulfuric acid (3.06 g concentrated sulfuric acid, 98%) and 10% PVA (30 g) were added into reverse osmosis water to make a 300-ml new method PVA slurry solution as in Tables 3 and 4. In Table 3 using NaCl as a hardening solution, which are significantly improved from gel beads disclosed in U.S. provisional application No. 63/003,516, April 2020, which is incorporated herein by reference. It is observed there that the pretreatment using sulfuric acid will make the gel beads bigger, softer, and more translucent than usual, indicating the physical structure is weak. However, these disadvantages can be corrected by embodiments of this invention so that the color can be observed whiter if the hardening cation ion concentration increases to more than 0.5%. Results in Table 4 show a similar experiment except that the hardening solution was changed to NH4Cl instead of NaCl. The ammonium chloride can make gel beads whiter with even only the small amount of 0.1%. Both of the hardening solutions, NaCl or NH4Cl, can keep gel beads dispersed in water. The hardness of 0.017 kg/cm2 can be achieved with an average diameter of 3.32 mm±0.028.
In this embodiment, unheated neutral ether-type PU was added to a PVA slurry solution before or after heating so that the leakage of PVA oligomer in PVA gel beads will not occur under a stress test using aeration with coarse air bubbles. Table 5 shows that using 6.7% PVA and 18% PU hardened in phosphates and NaCl can make a white and glossy surface with a little hardness of 0.005 kg/cm2. Lot No. 94 shows that there was no leakage of PVA oligomer under a stress test even though the hardening procedure was eliminated. Table 6 shows the gel beads significantly shrank in bead-forming solution if PU was heated and added into a PVA slurry solution. The PVA gel mixed with heated PU became opaque, like paste, and highly viscous (a viscosity of 5080 CPS measured under similar pretreatment condition as seen in Lot No. 11). Its appearance was also manifested in the rotating speed of the peristaltic pump that was used in the dropping technique for production of gel beads. Table 6 also shows that the size of PVA gel beads with heated PU changed from 2.7 mm to a larger 4 mm. Embodiments of these gel beads made with heated PU lose the glossy surface and the gel beads become softer as compared to PVA gel beads with unheated PU. Consequently, exemplary embodiments with the PU unheated provides different and more advantageous results for some applications compared 10 to heated PU. The 12% PVA with 2.75% unheated PU also showed good characteristics for the PVA gel beads as seen in Table 7 Lot No. 104.
In this embodiment, the PVA gel beads pretreated with NaH2PO4 and processed by a PVA-boric acid method were transferred separately into aqueous solutions of NaCl with varying concentration of 0.5, 1, 2, 3, 4, 5, 10, 20 and 25% and kept therein for 60 minutes. These beads were then removed from the solutions and rinsed with water. Diameter and hardness measurements were taken for ten PVA beads from each group. The remaining beads were put in 1000-mL air sparger for aeration stress tests. During aeration, 1000 mL/min of air was aerated for a week, after which the beads were removed for physical property measurements.
The properties of the gel beads of this example would be improved by application of the use of PU, etherification compounds and/or anions or anion releasing compounds to the making of the gel beads.
In this embodiment, PVA gel beads pretreated with NaH2PO4 and processed by a PVA-boric acid were transferred separately into aqueous hardening solutions of KCl with varying concentration of 0.5, 1, 2, and 3% and kept therein for 60 minutes. Table 9 shows that the diameters of the beads decreased with increased conductivity of the KCl solution, and the hardness of the beads also increased. After an aeration stress test, the beads which were hardened in solutions with a concentration of at least 1% maintained their white spherical appearance. However, the beads which were hardened in the solution with a concentration of 0.5% became translucent after aeration a stress test. These gel beads have some leakage of microorganisms from the gel beads.
The properties of the gel beads of this example would be improved by application of the use of PU, etherification compounds and/or anions or anion releasing compounds to the making of the gel beads.
In this embodiment, the PVA gel beads pretreated with NaH2PO4 and processed by a PVA-boric acid method were transferred separately into aqueous solutions of CaCl2 with varying concentration of 0.25, 0.5, 1, 2, 3, 5, and 10% and kept therein for 60 minutes. Table 10 shows that the diameters of the beads decreased with increased conductivity of the CaCl2 solution when the concentration was lower than 3%, and the hardness of the beads increased. After the aeration stress test, the beads that were hardened in solutions with concentrations between 0.5 and 2% maintained their white spherical appearance. Beads which were hardened in solutions with concentrations of 0.25%, 3% and higher became translucent after the aeration stress test. These gel beads have some leakage of microorganisms from the gel beads.
The properties of the gel beads of this example would be improved by application of the use of PU, etherification compounds and/or anions or anion releasing compounds to the making of the gel beads.
In this embodiment, a pilot plant was operated using this invention. A PVA-boric acid method was used, including the use of an aqueous solution (150 kg) containing 10% by weight of PVA that was mixed thoroughly with a concentrated sludge solution (3 kg) containing microorganisms (sludge concentration>6 g/L). The PVA gel beads were transferred into aqueous solutions of MgSO4 with a conductivity of 155.3 mmho/cm and kept therein for 90 minutes. These beads were then removed from the solution and rinsed with water. The hardness of the beads was 0.44 kg/cm2. The average diameter of the beads was 3.14±0.08 mm.
In this example, 150 kg of the beads were added into a 3.2-m3 airlift pilot bioreactor for advanced wastewater treatment in a petrochemical factory located in an Industrial Park. The wastewater to be treated was the effluent of the wastewater plant in the factory. The target effluent COD (chemical oxygen demand) concentration of the advanced treatment was below 250 mg/L to secure the effluent to meet the Industrial Management Center Wastewater Effluent Standard, COD below 480 mg/L. The hydraulic retention time was 20-24 hrs. The reaction was performed outdoors without temperature or pH control.
The field test failed once because the PVA gel beads dissolved. In the second trial a post treatment using MgSO4 was adopted. These gel beads still have some leakage of PVA (less than 5%) from the gel beads that is not obvious in the wastewater. However, we could observe the foaming to see if there is leakage under the stress test. Without the sulfuric acid or PU step in the pretreatment, it was observed that foaming of about 12 cm occurred during the stress test. On the other hand, with gel beads with the sulfuric acid or PU pretreatment according to an embodiment of this invention, the foaming is less then 1 cm under a stress test. This indicates that with the pretreatment of embodiments of this invention, the leakage is minimized.
In another embodiment of a pilot plant, a PVA-boric acid method was used with immobilized sludge as in Example 8 except that the gel beads were transferred into a 1% of NaCl solution with a conductivity of 21.5 mmho/cm and kept therein for 120 minutes. The average diameter of the beads was 4.37±0.22 mm. About 15 kg of the beads were added into one of the dual 100-L bioreactors for a wastewater treatment test in a petrochemical factory. The same target wastewater for IS and SS was coming from the outlet of an anaerobic system of the factory's wastewater treatment system. The hydraulic retention time was 8 to 12 hours. The reaction was performed outdoors without temperature or pH control for three months.
Therefore, the properties of the gel beads discussed in this example for the plant treatment and the zebra fish would have been improved by the application of the PU, etherification and/or anions or anion releasing compounds of this invention.
In this embodiment, the unheated PU/PVA gel beads were used to cultivate algae, nitrifiers from a local petrochemical activated sludge system, and pure denitrifying culture purchased from Azoo (New Taipei City, Taiwan). The composition of PU/PVA gel beads is 10% PVA (36 g) and 2.3% PU (15g with 55% solid content) in the mixture of 285-mL reverse osmosis water and 60-mL microorganism solution (2 g/L). The results show the algal growth within 2-3 days. Cultivation of nitrifiers shows pink color in the bottom of the tank. The urea fed with 800 mg/L was utilized completely in a 1-liter air sparger during 3-day fed-batch cultivation. The denitrification process emitted nitrogen and the PU/PVA gel beads floated on the water surface. The concentration of NO3 was completely utilized under 2-day fed-batch cultivation. This is evidence that the improvement of the physical and chemical structure of PU/PVA gel beads of this invention does not have the previous drawbacks and permits the mass transfer capability of immobilized substances such as microorganisms for being used in the biological field.
Although the present invention has been described with reference to teaching, examples and preferred embodiments, one skilled in the art can easily ascertain its essential characteristics, and without departing from the spirit and scope thereof can make various changes and modifications of the invention to adapt it to various usages and conditions. Those skilled in the art will recognize or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are encompassed by the scope of the present invention.
All publications, patents, and applications mentioned in this specification are herein incorporated by reference.
This application claims the benefit of U.S. Provisional Patent Application No. 63/003,516, filed Apr. 1, 2020, which is incorporated by reference herein in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2020/035822 | 6/3/2020 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63003516 | Apr 2020 | US |
