High Performance Photothermal Conversion Materials, Membrane, Layer Structure and Applications Thereof

Abstract

Present invention is related to a high performance photothermal conversion materials, membrane, layer structure and applications thereof. The said materials comprise an UV and infrared absorbed material and a visible light absorbed material with at least one of or both of these materials has photothermal conversion ability. These materials could be further produced as a porous membrane or foam layer with a plastic material. Further by layered with another hydrophilic fiber layer, a porous layer structure could be obtained by the present invention with high performance photothermal conversion, uni-direction water transportation and photocatalytic abilities. The present invention could absorb a wide range of light source (UV-to-vis-to-NIP) and convert to another energy like heat solving the insufficiency of conventional photothermal conversion material.

Claims

1. A photothermal conversion material comprising: a composite selected from the following two groups: an ultraviolet light and infrared light absorbing material is selected from the group consisting of tungsten oxide, titanium oxide, copper sulfide or carbon-containing material; and a visible light absorbing material is selected from the group consisting of Iron oxide, Carbon nitride, or precious metals.

2. The photothermal conversion material as claimed in claim 1, wherein: the tungsten oxide further comprises tungsten bronze; the carbon-containing material comprises graphite, graphene or carbon tube; and the precious metals comprises gold or silver.

3. The photothermal conversion material as claimed in claim 2, wherein: the tungsten bronze comprises rubidium tungsten bronze or cesium tungsten bronze.

4. The photothermal conversion material as claimed in claim 1, wherein: the photothermal conversion material has photocatalystic ability.

5. The photothermal conversion material as claimed in claim 2, wherein: the photothermal conversion material has photocatalystic ability.

6. The photothermal conversion material as claimed in claim 1, wherein the photothermal conversion material is in a form of porous fibrous membrane or porous foamed membrane by a plastic material.

7. The photothermal conversion material as claimed in claim 2, wherein the photothermal conversion material is in a form of porous fibrous membrane or porous foamed membrane by a plastic material.

8. The photothermal conversion material as claimed in claim 3, wherein the photothermal conversion material is in a form of porous fibrous membrane or porous foamed membrane by a plastic material.

9. The photothermal conversion material as claimed in claim 4, wherein the photothermal conversion material is in a form of porous fibrous membrane or porous foamed membrane by a plastic material.

10. The photothermal conversion material as claimed in claim 6, wherein the plastic material comprises polyvinylidene fluoride or triacetate cellulose.

11. The photothermal conversion material as claimed in claim 7, wherein the plastic material comprises polyvinylidene fluoride or triacetate cellulose.

12. The photothermal conversion material as claimed in claim 8, wherein the plastic material comprises polyvinylidene fluoride or triacetate cellulose.

13. The photothermal conversion material as claimed in claim 9, wherein the plastic material comprises polyvinylidene fluoride or triacetate cellulose.

14. A photothermal conversion material complex comprising: a thermal conversion material as a membrane as claimed in claim 1 being laminated onto a hydrophilic fibrous layer.

15. The photothermal conversion material complex as claimed in claim 14, wherein the hydrophilic fibrous layer comprises polyvinyl alcohol, polyester or polyurethane.

16. The photothermal conversion material complex as claimed in claim 14, wherein the thermal conversion membrane and/or the hydrophilic fibrous layer has gradients of porous or contact angle from the material to have gradient hydrophilic and hydrophobic structure.

17. The photothermal conversion material complex as claimed in claim 15, wherein the thermal conversion membrane and/or the hydrophilic fibrous layer has gradients of porous or contact angle from the material to have gradient hydrophilic and hydrophobic structure.

18. The photothermal conversion material complex as claimed in claim 14, wherein the complex is applied to sewage treatment or seawater desalination.

19. The photothermal conversion material complex as claimed in claim 15, wherein the complex is applied to sewage treatment or seawater desalination.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] The steps and the technical means adopted by the present invention achieve the above and other objects can be best understood by referring to the following detailed description of the preferred embodiments and the accompanying drawings.

[0016] FIG. 1A is an illustration of a photothermal conversion material in accordance with the present invention.

[0017] FIG. 1B is a closed-up view of FIG. 1A regarding the fiber composed of the photothermal conversion material in accordance with the present invention.

[0018] FIG. 2 is a SEM figure illustrating porous fiber composed of the photothermal conversion material in accordance with the present invention.

[0019] FIG. 3 is an illustration of usage for the photothermal conversion material in accordance with the present invention.

[0020] FIG. 4 is an illustration of hydrophilic and hydrophobic gradients structure of the photothermal conversion material complex in accordance with the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0021] Reference will now be made in detail to the present preferred embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers are used in the drawings and the description to refer to the same or like parts. It is not intended to limit the method by the exemplary embodiments described herein. In the following detailed description, for purposes of explanation, numerous specific details are set forth in order to attain a thorough understanding of the disclosed embodiments. It will be apparent, however, that one or more embodiments may be practiced without these specific details. As used in the description herein and throughout the claims that follow, the meaning of “a”, “an”, and “the” may include reference to the plural unless the context clearly dictates otherwise. Also, as used in the description herein and throughout the claims that follow, the terms “comprise or comprising”, “include or including”, “have or having”, “contain or containing” and the like are to be understood to be open-ended, i.e., to mean including but not limited to.

[0022] The present invention first provides a full-spectrum high performance photothermal conversion material comprising an ultraviolet light and infrared light absorbing material, and a visible light absorbing material, the ultraviolet light and infrared light absorbing material and/or the visible light absorbing material has an ability of absorbing a light source and converting it into another kind of energy, such as thermal energy.

[0023] The ultraviolet light and infrared light absorbing material in the present invention comprises tungsten oxide, titanium oxide (TiO), copper sulfide (CuS) or carbon-containing material. The visible light absorbing material includes Iron oxide, Carbon nitride, or precious metals such as gold or silver. The carbon-containing material comprises graphite, graphene or carbon tube, or other likely materials.

[0024] The aforementioned Titanium oxide (TiO), Copper sulfide (CuS) or carbon-containing materials in the present invention may already have the ability to absorb a light source in full-spectrum, and can be combined with other single light source absorbing materials to form a composite material achieving a more comprehensive full spectrum absorption efficiency.

[0025] The preferred embodiment of the present invention includes the ultraviolet light and infrared light absorbing material with the content in mole ratios ranging from 1:2 to 5:1, such as tungsten oxide (tungsten oxide (WO.sub.x) or tungsten bronze (M.sub.xWO.sub.3), where x may be 0.01-100), and the visible light absorbing material, such as a composite material obtained from one or more of following two components: iron oxide (Fe.sub.3O.sub.4) or carbon nitride (g-C3N4). The tungsten oxide includes tungsten trioxide Wo.sub.3 or WO.sub.2.72. The tungsten bronze includes rubidium tungsten bronze (Rb.sub.xWO.sub.3, where x may be 0.01-100) or cesium tungsten bronze (Cs.sub.xWO.sub.3, Cs.sub.0.32WO.sub.3, where x may be 0.01˜100). The photothermal conversion material of the present invention can have a variety of structural types, including nanoparticles, nanorods, nanowires, nanobundles, and nanocrystals or Urchin-like spheres.

[0026] The photothermal conversion material in the present invention has the ability to absorb the photon energy from the full-spectrum (UV-to-vis-to-NIP) wavelength, and can efficiently convert light energy directly into heat energy under light illumination. On the other hand, the tungsten compound in the present invention contains tungsten oxide (WO.sub.x) or tungsten bronze (M.sub.xWO.sub.3) components, which have ultraviolet light, infrared light and enhanced near-infrared absorption capabilities. The tungsten bronze is M.sub.xWO.sub.x produced by doping metal elements in tungsten oxide to enhance the light absorption in the solar spectrum, or strong local surface plasmon resonance (LSPR) and interval charge transfer (oxidation from W6.sup.+ to W5.sup.+ state). By mixing this type of tungsten material with other materials, a full-spectrum photocatalyst with advanced light absorption efficiency are formed.

[0027] With reference to FIGS. 1A and 1B, the aforementioned photothermal conversion material 111A and a suitable plastic material 111B are formed as an electrospinning, solution with a concentration ranging from 1 wt % to 20 wt %, more preferably between 3 wt % to 10 wt %. An electrospinning process is utilized to form a composite electrospun fiber 111 to form a composite electrospun fiber layer 11. Further the composite electrospun fiber layer 11 is laminated on a hydrophilic fibrous layer 13 formed from a hydrophilic fiber 131 to form a photothermal conversion composite layer structure 10.

[0028] The plastic material 111B preferably contains polyvinylidene fluoride (PVDF) or triacetate cellulose (TAC), more preferably the TAC could be recycled triacetate cellulose (r-TAC) and the like. The photothermal conversion material 111A and the plastic material 111B are mixed to form an electrospinning liquid using electrospinning technology to produce the composite electrospun fiber layer 11 on the hydrophilic fibrous layer 13. The hydrophilic fibrous layer 13 is preferably to be polyvinyl alcohol (PVA), modified hydrophilic polyester or polyurethane (PU). The modified hydrophilic polyester comprises a non-woven fabric of ethylene terephthalate (PET) fiber.

[0029] On the other hand, the photothermal conversion material 111A and the plastic material 111B are electrospun to produce the composite electrospun fiber layer 11. The composite electrospun fiber layer 111 is preferably to have its fiber with porous structure as shown in FIG. 2. The plastic material 111B is used as a polymer matrix providing the composite electrospun fiber layer 11 hydrophobic and moisture-permeable abilities.

[0030] It is worth noticed that the composite electrospun fiber layer 111 as mentioned above is only a preferred embodiment of the present invention. However, the photothermal conversion material 111A and a compatible plastic 111B could also be used by other processes such as melt-blown technique to form a porous fiber membrane layer, or a foaming process to form a porous foamed membrane layer and further laminated on the hydrophilic fibrous layer 13 to form the photothermal conversion composite layer structure 10 as described by the present invention.

[0031] With reference to FIG. 3, the photothermal conversion layer structure 10 of the present invention is preferably used for the function of driving water evaporation by the hydrophilic fibrous layer 13 contacting with any treating liquid surface W. As such, the hydrophilic fibrous layer 13 will continue to absorb moisture into the fiber from the treating liquid surface, and the photothermal conversion composite layer structure 10 on the upper layer to directly absorb light sources from an external environment, such as solar energy to convert light energy into heat. By using that generated heat, the moisture can gradually evaporate from the treating liquid surface W. The photothermal conversion composite layer structure 10 accelerates the effect of moisture evaporation. Because the photothermal conversion composite layer structure 10 provided by the present invention is a combination of hydrophilic and hydrophobic layers, the hydrophilic layer contacting the treating liquid surface W to allow the liquid being unidirectionally moved to the hydrophobic layer and eventually dispersed or evaporated.

[0032] More preferably, the unidirectional moisture conductivity of the photothermal conversion composite layer structure 10 can be further achieved through the hydrophilic and hydrophobic gradients between structures in each layer. With reference to FIG. 4, by using multiple layers of the hydrophobic layer 13 (for example three layers as shown in FIG. 4) with its composed hydrophobic fiber with different contact angle/materials to have the so-called hydrophobic gradient. The composite electrospun fiber layer 11 can also have similar design with multiple layers (for example three layers as shown in FIG. 4) with different degree of hydrophilic ability achieving from different porosity. The hydrophilic and hydrophobic gradient effect would allow the present invention to have a better unidirectional moisture conductivity.

[0033] The structural engineering strategies of the photothermal conversion composite layer structure 10 provided by the present invention comprises but not limited to: light absorption and light conversion engineering, thermal localization and thermal conductivity, waterway design, interface engineering, bionic structure design, 3D evaporator design and salt discharge structure design, etc. The present invention has a broad band or full-spectrum light absorption ability and high efficiency photothermal conversion ability, and has good heat insulation and high efficiency water transmission efficiency.

EMBODIMENT 1

Synthesis of Rb.SUB.x.WO.SUB.3.—Fe.SUB.3.O.SUB.4 .Nanocomposite

[0034] 0.5952 g of WCl.sub.6 was continuously stirred for 15 minutes and dissolved in absolute ethanol, and then 0.076 g of RbOH was added. Then add 24 mL of acetic acid to the mixed solution at 240° C. and put it in an sterilizer lined with Teflon lining for 20 hours. The solution was taken out of from the sterilizer, centrifuged and dried in an oven at 60° C. to obtain Rb.sub.xWO.sub.3.

[0035] Next, 0.2 g of the above-mentioned Rb.sub.xWO.sub.3 was dispersed and dissolved in 20 mL of absolute ethanol using ultrasonic and stirred for 1 hour. In the suspension, add 0.5 mol (mole) of Fe.sub.3O.sub.4 nanoparticle in ethanol solution 20 mL and stir quickly. The suspension was then centrifuged and dried in an oven at 60° C. for 1 hour.

[0036] Preparation of Rb.sub.xWO.sub.3—Fe.sub.3O.sub.4 Nanocomposite Electrospun Fiber Membrane and Photothermal Conversion Composite Layer Structure

[0037] The aforementioned Rb.sub.xWO.sub.3—Fe.sub.3O.sub.4 nanocomposite was stirred at a ratio of 9:1 (v/v) and completely dissolved in 5 wt % rTAC to form an electrospinning solution. The electrospinning solution was further applied to electrospinning process at a voltage of 15 kV, a flow rate of 0.5 ml/h, and a distance between needle tip and collector is 15 cm, and the Rb.sub.xWO.sub.3—Fe.sub.3O.sub.4 nanocomposite and rTAC as plastic material are spun on the PET non-woven fabric to obtain the photothermal conversion composite layer structure of the present invention.

EMBODIMENT 2

[0038] Synthesis of WO.sub.2.72—Fe.sub.3O.sub.4 Nanocomposite

[0039] Dissolve 0.7 g of WCl.sub.6 in 70 mL of absolute ethanol and continuous stirring for 15 minutes to obtain a yellow solution. At the same time, take another container to add 0.231 g of Fe.sub.3O.sub.4 powder to 50 mL of absolute ethanol and stir with ultrasonic to obtain a black solution.

[0040] The yellow solution and the black solution were mixed and placed in a sterilizer with a Teflon lining and heated in an oven at 180° C. for 24 hours. The suspension was then centrifuged and dried in an oven at 60° C. for 8 hours.

[0041] Preparation of WO.sub.2.72—Fe.sub.3O.sub.4 Nanocomposite Electrospun Fiber Membrane and Photothermal Conversion Composite Layer Structure

[0042] The aforementioned WO.sub.2.72—Fe.sub.3O.sub.4 was stirred at a ratio of 250 g and completely dissolved in 5 wt % rTAC to form an electrospinning solution. The electrospinning solution is applied to the electrospinning process at a voltage of 15 kV a relative humidity of 50%, a flow rate of 0.5 ml/h, and a distance between needle tip and collector is 15 cm. WO.sub.2.72—Fe.sub.3O.sub.4 nanocomposite and rTAC as being plastic material are spun on the PVA non-woven fabric to obtain the photothermal conversion composite layer structure 10.

EMBODIMENT 3

[0043] Synthesis of Cs.sub.0.32-gC.sub.3N.sub.4 Nanocomplex

[0044] gC.sub.3N.sub.4 was dissolved in 40 mL of ethanol and stirred for 1 hour. Next, add 0.297 g of WCl6 and vigorous stirring and mixing well.

[0045] Add 0.065 g of CSOH.Math.H2) to the above suspension and stir for 7 minutes. Further, 10 mL of acetic acid was added, and the suspension was placed in a sterilizer lined with Teflon and heated in an oven at 240° C. for 20 hours for reaction. After the reaction was completed, it was cooled to room temperature, and the resulting product was washed with ethanol 4 times, and then dried at 60° C. for 8 hours to obtain a Cs0.32-gC.sub.3N.sub.4 nanocomposite.

[0046] Preparation of the Cs.sub.0.32-gC.sub.3N.sub.4 Nanocomposite Electrospun Fiber Membrane and Photothermal Conversion Composite Layer Structure

[0047] The aforementioned. Cs0.32-gC.sub.3N.sub.4 nanocomposite was mixed in a dimethylformamide solution (Dimethylformamide, DMF) with ultrasonic for 1 hour, then 2.2 g of PVDF particles were added and heated and stirred at 120° C. for 2 hours and obtain an electrospinning solution after cooling. Then, the electrospinning liquid is electrospun on the PVA non-woven fabric to obtain the photothermal conversion composite layer structure 10.

[0048] <Validation Tests>

[0049] First, a UV-VIS-NIR spectrometer is used to perform a full-spectrum light energy absorption test to above three embodiments provided by the present invention as shown in Chart 1 below.

TABLE-US-00001 CHART 1 full spectrum light absorption ability Type of light source Embodiment UV light Visible light Near infrared light Embodiment 1 Absorbed Absorbed Absorbed Embodiment 2 Absorbed Absorbed Absorbed Embodiment 3 Absorbed Absorbed Absorbed

[0050] Next, several thermal properties tests are performed to prove that the present invention has the ability to generate heat for evaporating moisture. The results are shown as Chart 2 below.

TABLE-US-00002 CHART 2 Thermal properties Thermal abilities Thermal Thermal Thermal Thermal conductivity diffusivity absorption resistance Embodiment (mW/m .Math. K) (mm.sup.2/s) (Ws.sup.1/2/m.sub.2K) (m.sup.2mK/W) Embodiment 1 28.10 0.13 78.17 21.20 Embodiment 2 At least At least At least At least 27.00 0.13 78.17 21.20 Embodiment 3 27.00 At least At least At least 0.13 78.17 21.20 Comparation 25.60 0.30 49.20 22.60 embodiment (Pure rTAC film)

[0051] The present invention also performs several tests for validating the conversion efficiency of light energy conversion and moisture evaporation with the photothermal conversion composite layer structure 10 at the treating liquid surface W as shown in Chart 3 below. By laying the preferred embodiments of the present invention on the surface of the treating liquid surface, the results show that the present invention has a strong interface heating ability, and a hot zone is obviously generated at the air-water interface under the light source, and the temperature of the water interface increases with treatment time of the light source. Under such thermal environment, the present invention successfully generates heat letting the water surface evaporated by the unidirectional layered structure. The present invention also has the excellent light-to-heat conversion efficiency under solar radiation and has stable performance and durability during multiple cycles showing that the present invention has the potential to be successfully introduced into the market.

TABLE-US-00003 CHART 3 Photothermal conversion efficiency Conversion Moisture weight loss Light Comparison of after 35 minutes of Evaporation conversion light source types exposure to light source rate/hour efficiency for photothermal Number of Embodiment (kg/m.sup.2) (kg/m.sup.2h) (%) effect cycles Embodiment 1 1.3 3.56 89.3 Solar energy > 15 NIR > Visible light Embodiment 2 At least At least At least Solar energy > 15 1.3 3.56 89.3 NIR > Visible light Embodiment 3 1.5 2.70 95.3 Solar energy > 12 NIR > Visible light Comparation embodiment  ,  0.60 1.44 — — —    Water surface without applying any light-to-heat conversion structure

[0052] The present invention has the ability of photothermal conversion with unidirectional structure which is particularly suitable for applications in seawater desalination or desalination. By using the preferred embodiments provided by the present invention, the salt ion content in sea water and the collected condensate water before and after the treatment are shown in Table 4. The present invention has the ability to treat sea water into drinking water (according to the definition of the salt ion content in drinking water by the World Health Organization) proving that the present invention does have excellent desalination ability.

TABLE-US-00004 CHART 4 Treatment status Before treatment After treatment Content of the irons (seawater) (drinking water) Na.sup.+ 27500 ppm  3.23 ppm K.sup.+ 1000 ppm  2.4 ppm Mg.sup.2+ 5300 ppm 0.17 ppm Ca.sup.2+ 1200 ppm 2.38 ppm

[0053] On the other hand, the photothermal conversion composite layer structure 10 provided by the present invention also has the ability to photocatalytically decompose heavy metal components. For example, the treated water also contains the pollutants like nitrophenol, tetracycline (tetracycline), methylene blue/orange (methylene blue/orange, MB/MB) and rhodamine B (rhodamine B) or these pollutants combination. The purified condensate water is tested to be colorless and transparent, and the pollutant content in the tested water is almost in zero content. The porous fiber structure of the present invention has the function of adsorbing pollutants, and the photothermal conversion material has the ability to convert organic pollutants, such as but not limited to hexavalent chromium (Cr(VI)) into non-toxic trivalent chromium (Cr(III)) and maintained in the porous membrane without returning to the water achieving the effect of sewage purification.

[0054] The foregoing descriptions are only preferred embodiments of the present invention, and are not intended to limit the scope of rights claimed by the present invention. All other equivalent changes or modifications completed without departing from the spirit disclosed by the present invention shall include Within the scope of the patent application of the present invention.