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Bio-waste-derived nanofibers formed by solution blowing and their applications as biomedical materials and adsorbents for heavy metals removal from polluted water.

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Bio-waste-derived nanofibers formed by solution blowing and their applications as biomedical materials and adsorbents for heavy metals removal from polluted water.

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Plenary lecture given by Prof. Alexander Yarin (University of Illinois at Chicago, USA) on September 11, 2017 in Gramado (Brazil) during the XVI B-MRS Meeting.

Plenary lecture given by Prof. Alexander Yarin (University of Illinois at Chicago, USA) on September 11, 2017 in Gramado (Brazil) during the XVI B-MRS Meeting.

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Bio-waste-derived nanofibers formed by solution blowing and their applications as biomedical materials and adsorbents for heavy metals removal from polluted water.

  1. 1. Alexander L. Yarin Department of Mechanical and Industrial Engineering University of Illinois at Chicago U.S.A. University of Illinois at Chicago
  2. 2. 2 Acknowledgements This work was supported by a research contract with the United Soybean Board, Chesterfield, Missouri (research contract no. 0491). This work is supported by the Nonwovens Institute, grant No. 14-161. University of Illinois at Chicago PhD students from the UIC Multiscale Mechanics and Nanotechnology Lab involved in this work: Y. Zhang S. Sinha-Ray Sh. Khansari A. Kolbasov S. Sett Postdocs: Dr. M.W. Lee Dr. S. Duzyer Dr. S. An Collaborators: Dr. B. Pourdeyhimi (North Carolina State University), Dr. K. Stephansen (Technical University of Denmark) Dr. S.S. Yoon (Korea University)
  3. 3. Outline • Solution Blowing of Bio-Waste Derived Nanofibers • Mechanical Behavior of Soy Protein-Based Nanofiber Mats • Plant- and Animal-Based Nanofibers • Effect of Chemical and Physical Crosslinking on Mechanical Properties of Soy Protein-Based Nanofiber Mats • Controlled Drug Release (Desorption) from Soy Protein-Based Nanofiber Mats • Protection of Pruned Vines from Esca Fungi • Prevention of Mold Invasion • Antibacterial Action • Heavy Metal Ion Adsorption on Biopolymer Nano-Textured Membranes • Conclusion 3 University of Illinois at Chicago
  4. 4. Plant- and Animal-Based Protein Biopolymers Biofuel Byproducts Cellulose Cellulose Acetate ZeinSoy Protein Silk Sericin Lignin Bovine Serum Albumin, Fish Protein, Chitosan 4 University of Illinois at Chicago
  5. 5. 5 Plant-Based Biopolymers’ Applications University of Illinois at Chicago • Biodiesel • Bioplastic • Drug Delivery • Wound Dressing • Disinfectants • Adhesives • Films • Textile • Clear Tapes • Glass Frames • Cigarette Filters • Additives • Coatings • Carbon Fiber • Paper Industry • Cosmetics • Adsorbents
  6. 6. Even cars: 6 University of Illinois at Chicago
  7. 7. Solution Blowing of Bio-Waste Derived Nanofibers Solution blowing setup to produce monolithic and core-shell nanofibers • Sinha-Ray, S., Yarin, A. L., Pourdeyhimi, B., 2010, Carbon 48, 3575-3578. • Sinha-Ray, S., Zhang, Y., Yarin, A.L., Davis, S., Pourdeyhimi, B., 2011, Biomacromolecules 12, 2357-2363. • Khansari, S., Sinha-Ray, S., Yarin, A.L., Pourdeyhimi, B., 2012, Journal of Applied Physics 111, 044906-1-13. 7 University of Illinois at Chicago
  8. 8. Schematic of Solution Blowing Process
  9. 9. Sample Preparation Nanofibers are collected on rotating aluminum drum and cut into rectangular pieces of 10-25 mm wide and 20-40 mm long. Nanofiber mat thickness is 0.20-0.30 mm. Solution-blown sample of soy protein/nylon 6 (70/30 wt/wt%).
  10. 10. Single-nozzle Solution Blowing
  11. 11. Macroscopic Images of Soy Protein Nanofibers Average diameter of nanofibers is 300-500 nm.
  12. 12. Microscopic Optical Images of Soy Protein Nanofibers: SP/Nylon 6 Nanofibers Blown from Solution in Formic Acid
  13. 13. Microscopic Optical Images of Soy Protein Nanofibers: SP/PVA Nanofibers Blown from Aqueous Solution
  14. 14. From Single-Nozzle to Eight-Nozzle Solution Blowing
  15. 15. 45 wt% Soy Protein-Nylon 6 Nanofiber Mat: 6 Nozzles for 5 Minutes
  16. 16. Industrial-Scale Solution Blowing of Soy Protein Nanofiber Mats A. Kolbasov et al. Industrial & Engineering Chemistry Research 55, 323-333 (2016).
  17. 17. Industrial-Scale Soy Protein Nanofiber Mats
  18. 18. Solution-Blown Monolithic Nanofibers Containing 50% of Bio-Polymer (Soy Protein) S. Sinha-Ray, Y. Zhang, A.L. Yarin, S.C. Davis, B. Pourdeyhimi, Biomacromolecules, 12, 2357-2363 (2011).
  19. 19. Solution-Blown Core-Shell Nanofibers with Soy Protein in the Shell
  20. 20. Sample Preparation and Tensile Tests 100 N capacity Instron machine (model 5942) • Khansari, S., Sinha-Ray, S., Yarin, A.L., Pourdeyhimi, B., 2012, Journal of Applied Physics 111, 044906-1-13. 20 University of Illinois at Chicago
  21. 21. Stress-Strain Behavior for Soy Protein/Nylon 6 (40/60 wt%) Nanofiber Mats Failure stress and strain are in the range of σxx,rupture=0.4-0.9 MPa and εrupture=4-10%. • Khansari, S., Sinha-Ray, S., Yarin, A.L., Pourdeyhimi, B., 2012, Journal of Applied Physics 111, 044906-1-13. 21 University of Illinois at Chicago
  22. 22. Phenomenological rheological constitutive equation: For an incompressible material: Phenomenological Model σ=-PI+τ σ is stress tensor, P is hydrostatic pressure, and τ is deviatoric stress Constitutive equation for stress in elastic-viscopastic material: 22 University of Illinois at Chicago • M. B. Rubin and A. L. Yarin, 1993, J. Non-Newton. Fluid Mech. 50, 79; Corrigendum: 1995, J. Non-Newton. Fluid Mech. 57, 321.
  23. 23. Phenomenological Model 23 University of Illinois at Chicago • Prager, W. Duke Math. J. 9, 1942, 228. Prager Equation The phenomenological equation for the uniaxial stretching of a planar strip yields the following stress-strain dependence:
  24. 24. Stress-Strain Behavior of Soy Protein Nanofiber Mats Average width of the samples (mm) Average thickness of the samples (mm) Average Young’s modulus E (MPa) Average yield stress Y (MPa) Average specific strain energy u (MPa) Average maximum strain at rupture εrupture(%) Average maximum stress at rupture σxx,rupture 12.07 0.20 19.56±6.48 0.56±0.15 2.26±0.71 4.52±0.92 0.67±0.10 24 1, experiment 2, phenomenological model 1, experiment 2, phenomenological model University of Illinois at Chicago
  25. 25. for(φ,t): the orinetational probability density function in nanofiber mat. at t=0, for(φ,t) =1/2π Solution for(φ,t) is found from the Fokker-Planck equation: Micromechanical Model 25 University of Illinois at Chicago
  26. 26. Rupture of Individual Bonds in Mats under Uniaxial Stretching 26 University of Illinois at Chicago
  27. 27. 27 Mat Plasticity as Bond Rupture Process University of Illinois at Chicago
  28. 28. * fσ /E 0.047= 1-experiment 2,3,4-micromechanical model * fσ /E 0.058= * fσ /E 0.040= Soy protein/nylon 6 (40/60 wt/wt %) nanofiber mat’s stress-strain curve fitted with (a) phenomenological and (b) micromechanical models. Characterization of Stress-Strain Behavior for Soy Protein Nanofibers 28 University of Illinois at Chicago
  29. 29. Characterization of Stress-Strain Behavior for Soy Protein Nanofibers Sample Width (mm) Thickness (mm) Young’s modulus E (phenomenological model); MPa Young’s modulus E corresponding to the micromechanical model; MPa Yield stress of the phenomenological model, Y (MPa) 1 11.91 0.22 12.8 12.8 0.53 0.071 2 11.47 0.22 17.58 17.58 0.46 0.047 3 12.43 0.22 14.26 14.26 0.46 0.058 4 11.47 0.22 20.88 20.88 0.53 0.047 5 11.21 0.22 19.69 19.69 0.6 0.055 6 11.38 0.24 24.01 24.01 0.6 0.047 7 11.53 0.2 38.02 38.02 0.78 0.038 8 11.65 0.22 24.25 24.25 0.53 0.041 9 11.99 0.22 14.87 14.87 0.49 0.058 10 12.01 0.16 21.79 21.79 0.79 0.060 Relative bond rupture stress of the micromechanical model, * fσ /E 29 University of Illinois at Chicago
  30. 30. Average width of the samples (mm) Average thickness of the samples (mm) Average Young’s modulus E (MPa) Average yield Stress Y (MPa) Average specific strain energy u (MPa) Average maximum strain at rupture εrupture(%) Average maximum stress at rupture σxx,rupture 11.22 0.15 22.26±6.06 0.57±0.3 0.92±0.02 2.41±0.40 0.54±0.10 1-experiment 2-phenomenological model Characterization of Stress-Strain Behavior for Core/Shell Soy Protein Nanofibers 30 University of Illinois at Chicago
  31. 31. Characterization of Stress-Strain Behavior for Nylon 6 Nanofibers Average width of the samples (mm) Average thickness of the samples (mm) Average Young’s Modulus E (MPa) Average yield stress Y (MPa) Average specific strain energy u (MPa) Average maximum strain at rupture εrupture(%) Average maximum stress at rupture σxx,rupture 13.00 0.39 14.46±2.30 1.17±0.75 11.71±0.31 11.80±1.39 1.68±0.18 1-experiment 2-phenomenological model 31 University of Illinois at Chicago
  32. 32. 32 Biopolymer-Based Nanofiber Mats Cellulose Acetate/PAN (50/50 wt %) Cellulose Acetate/PAN (30/70 wt %) Soy Protein/Zein/Nylon 6 (25/25/50 wt %) Zein/Nylon 6 (57/43 wt %) Core/Shell Zein/Nylon 6 70 wt % zein in core Lignin/Nylon 6 (50/50 wt %) Zein/Silk Sericin/Nylon 6 (25/25/50 wt %) Silk Sericin/Nylon 6 (50/50 wt %) BSA/PVA (50/50 wt %) Cellulose Acetate/PAN (50/50 wt %) Soy Protein/Zein/Nylon 6 (25/25/50 wt %) Zein/Nylon 6 (57/43 wt %) Silk Sericin/Nylon 6 (50/50 wt %) Zein/Silk Sericin/Nylon 6 (25/25/50 wt %) Soy Protein/PET (20/80 wt %) BSA/PVA (50/50 wt %) Core/Shell Zein/Nylon 6 70 wt % zein in core University of Illinois at Chicago S. Khansari, S. Sinha-Ray, A.L. Yarin,B. Pourdeyhimi. Industrial & Engineering Chemistry Research 52, 15104-15113 (2013).
  33. 33. Solution-Blown Nanofibers from Fish Sarcoplasmic Protein 33 University of Illinois at Chicago Solution-blown FSP/nylon 6 fibers with dry weight ratios of (a) 10/90, (b) 25/75, (c) 50/50, (d) 75/25, (e) 90/10. S. Sett, K. Stephansen, A.L. Yarin. Polymer v.93, 78-87 (2016).
  34. 34. Mechanical Characterization of Biopolymer-Based Nanofiber Mats 34 University of Illinois at Chicago zein/nylon 6 (40/60 wt%) core/shell zein /nylon 6 (70 wt% zein in core) silk sericin/nylon 6 (50/50 wt%) soy protein/PET (20/80 wt%) zein/nylon 6 (57/43 wt%) zein/nylon 6 (66/34 wt%) soy protein/zein /nylon 6 (25/25/50 wt%) silk sericin/zein /nylon 6 (25/25/50 wt%) lignin/nylon 6 (25/75 wt%) lignin/nylon 6 (50/50 wt%), cellulose acetate /PAN (30/70 wt%) pure PET
  35. 35. 35 Sample Content (wt %) Solvent Ave. Width (mm) Ave. Thickness (mm) Ave. Young’s Modulus E; (MPa) Ave. Yield Stress Y; (MPa) Max. Strain at Rupture (%) Max. Stress at Rupture (MPa) Zein/Nylon 40/60 Formic acid 8.44 0.20 12.53±2.55 0.16±0.07 2.21±0.76 0.19±0.06 Zein/Nylon 57/43 Formic acid 6.47 0.20 3.38±1.69 0.10±0.02 5.56±1.44 0.13±0.02 Zein/Nylon 66/34 Formic acid 7.08 0.20 2.16±0.74 0.04±0.01 4.28±0.92 0.06±0.01 Core-Shell Zein Core: 70/30 Formic acid 6.44 0.20 6.05±0.69 0.30±0.01 12.22±0.62 0.47±0.03 SP/Zein/Nylon 25/25/50 Formic acid 6.93 0.20 10.90±2.54 0.23±0.04 5.63±2.37 0.35±0.06 Zein/Silk Sericin/Nylon 25/25/50 Formic acid 6.50 0.15 20.46±4.88 0.24±0.05 2.50±0.49 0.35±0.60 Silk Sericin/Nylon 50/50 Formic acid 5.29 0.30 11.02±2.16 0.22±0.06 2.73±0.41 0.28±0.07 Lignin/Nylon 25/75 Formic acid 5.53 0.16 23.39±6.49 0.42±0.08 4.13±1.15 0.61±0.10 Lignin/Nylon 50/50 Formic acid 6.13 0.15 9.78±2.41 0.22±0.02 13.72±3.76 0.38±0.04 SP/PET 20/80 TFA/AC/ DCM 6.55 0.20 28.59±2.63 0.32±0.11 0.88±0.05 0.27±0.04 Cellulose AC/PAN 30/70 DMF 7.90 0.15 3.47±2.67 0.23±0.01 4.50±1.17 0.15±0.05 Pure PET 100 TFA/AC/ DCM 7.56 0.20 28.14±3.24 0.37±0.07 2.28±0.31 0.50±0.008 xx 8 2 E Y tanh 3 3 Y   =      σ ε Mechanical Properties for Biopolymer-Based Nanofiber Mats University of Illinois at Chicago
  36. 36. Crosslinking of Soy Protein Nanofiber Mats 36 Cross-linking Agents Formaldehyde Glyoxal Sodium Borohydride Zinc Sulfate • Sinha-Ray, S., Khansari, S., Yarin, A.L., Pourdeyhimi., B., 2012, Industrial and Engineering Chemistry Research 51, 15109-15121. University of Illinois at Chicago
  37. 37. (a) 20 wt% formaldehyde (b) 20 wt% glyoxal (c) 5 wt% of sodium borohydride (d) 10 wt% zinc sulfate (c) (d) The weight ratio of crosslinking agents to nanofiber samples is 5, 10, and 20 wt %. Soy protein/nylon 6 (50/50 wt %) nanofiber mat cross-linked at 80 wt % glyoxal/nanofiber mat ratio. Crosslinking of Soy Protein Nanofiber Mats 37 University of Illinois at Chicago
  38. 38. Mechanical Properties of Crosslinked Fibers using Formaldehyde and Zinc Sulfate 38 Formaldehyde Zinc Sulfate University of Illinois at Chicago
  39. 39. Rectangular pieces of nanofiber mats were heated under pressure for 1 min at 55 °C. 1- Non-bonded samples 2- Thermally-bonded samples Thermal Bonding of Soy Protein Nanofiber Mats 39 University of Illinois at Chicago
  40. 40. Wet Bonding for Soy Protein Nanofiber Mats Wet samples were compressed under the mass load of 150 g (i.e. under pressure of 6 kPa) for 24 h at room temperature until they were partially dried. 1- Non-treated samples 2- Wet-conglutinated samples 40 University of Illinois at Chicago
  41. 41. Controlled Drug Release from Soy Protein Nanofibers 41 University of Illinois at Chicago Monolithic Soy Protein/Nylon 6 (50/50 wt %) 1 wt % Rhodamine B fluorescent dye is incorporated in nanofiber mats. Core/Shell Soy Protein/Nylon 6 Monolithic Soy Protein/PVA (50/50 wt %) • Khansari, S., Duzyer, S., Sinha-Ray, S., Hockenberger, A., Yarin, A.L., Pourdeyhimi, B., 2013, Molecular Pharmeceutics 10, 4509-4526 . • Srikar, R., Yarin, A. L., Megaridis, C. M., Bazilevsky, A. V., Kelly, E., 2008, Langmuir 24, 965-974.
  42. 42. Soy Protein (50 wt%) Nanofibers Containing Rhodamine B Fluorescent Dye as a Model Drug vs. Riboflavin-Containing Nanofibers Sh. Khansari et al. Molecular Pharmaceutics 10, 4509-4526 (2013).
  43. 43. Images of Rhodamine B-Loaded Nanofibers 43 Before Water Immersion After Completion of Release Experiments Monolithic Nylon 6 Nanofibers Monolithic Soy Protein/Nylon 6 (50:50) Nanofibers Monolithic Soy Protein/PVA (50:50) Nanofibers Monolithic soy protein/nylon 6 + 10 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 Nanofibers Core/Shell Soy Protein/Nylon 6 +10 wt% PEG Nanofibers Before Water Immersion After Completion of Release Experiments University of Illinois at Chicago
  44. 44. 44 Rhodamine B Release Profiles from Nanofibers Nylon 6 Nanofibers Soy Protein/Nylon 6 Nanofibers Soy Protein/PVA Nanofibers Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Soy Protein/Nylon 6 +10 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 Nanofibers Core/Shell Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 +10 wt% PEG Nanofibers University of Illinois at Chicago
  45. 45. The Release Kinetics for the Desorption-Limited Mechanism Gt is the amount of dye/drug release by time t; α=Msd0/(Msd0+Mbd0) is the nanoporosity factor; Msd0 is the initial amount of dye/drug at the nanopore surface; Mbd0 is the initial amount of dye/drug in the fiber bulk; τr is the characteristic time for the release process. 45 University of Illinois at Chicago • Srikar, R., Yarin, A. L., Megaridis, C. M., Bazilevsky, A. V., Kelly, E., 2008, Langmuir 24, 965-974.
  46. 46. Experimental Rhodamine B Release Profiles vs. Predictions of the Desorption-Limited Theory 46 Nylon 6 Nanofibers Soy Protein/Nylon 6 Nanofibers Soy Protein/PVA Nanofibers Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Soy Protein/Nylon 6 +10 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 Nanofibers Core/Shell Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 +10 wt% PEG Nanofibers University of Illinois at Chicago
  47. 47. α1 and τr1 correspond to drug release from the existing pores, and α2 and τr2 correspond to the “release” of a leachable component of the fibers and thus, to drug release from the surfaces of the newly formed pores. Gt is the amount of dye released by time t. τr is the characteristic time of the release process. The Release Kinetics for the Two-Stage Desorption-Limited Mechanism 47 University of Illinois at Chicago
  48. 48. Experimental Rhodamine B Release Profiles vs. Two-Stage Desorption-Limited Mechanism 48 University of Illinois at Chicago Nylon 6 Nanofibers Soy Protein/Nylon 6 Nanofibers Soy Protein/PVA Nanofibers Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Soy Protein/Nylon 6 +10 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 Nanofibers Core/Shell Soy Protein/Nylon 6 +5 wt% PEG Nanofibers Core/Shell Soy Protein/Nylon 6 +10 wt% PEG Nanofibers
  49. 49. 49 Sample Average α1(%) Average τr1(min) Average α2(%) Average τr2(min) Average E1(kJ/mol) Average E2(kJ/mol) Monolithic Nylon 6 38.21±5.63 15.05±2.35 20.17±3.72 299.15±97.95 28.43±0.38 35.79±0.6 SP/Nylon 49.23±7.22 23.4±3.46 10.79±3.09 199.31±40.66 29.53±0.38 34.85±0.26 SP/Nylon+5%PEG 66.52±3.84 20.55±1.46 15.19±1.24 191.58±25.17 29.23±0.17 34.78±0.1 SP/Nylon+10%PEG 56.8±1.63 38.37±6.56 36.77±1.31 490.29±180.73 30.75±0.45 37.59±0.04 Core/Shell SP/Nylon 36.98±0.84 20.96±2.71 15.66±2.72 362.07±14.04 29.26±0.31 36.39±+0.02 SP/Nylon+5%PEG 38.4±3.98 13.67±9.88 19.38±1.16 396.03±182.93 25.13±5.6 36.31±1.55 SP/Nylon+10%PEG 30.41±4.34 20.2±7.21 33.94±3.52 607.20±132.24 29±1.01 37.61±0.34 Two-Stage Desorption-Limited Mechanism Parameters University of Illinois at Chicago
  50. 50. Pruned Vines Affected by Esca Fungi Western Farm Press, July 1, 2017; http://www.westernfarmpress.com/grapes/grapevine-canker-disease -impacts-california-vineyards
  51. 51. Protection of Pruned Vines from Esca Fungi
  52. 52. Electrospun Biopolymer Membranes for Protection of Pruned Vines from Esca Fungi S. Sett, M.W. Lee, M. Weith, B. Pourdeyhimi, A.L. YarinJ. Materials Chem. B 3, 2147-2162 (2015).
  53. 53. Protection of Pruned Vines from Esca Fungi Rayon/soy protein/PCL nanofiber membranes; The scale bars are 25 µm.
  54. 54. Electrosprayed Food Adhesives
  55. 55. Delamination and Adhesion (a) 180º peeling test of samples using Instron machine. (b) Dead weight test.
  56. 56. Normal Adhesive Energy
  57. 57. Shear Adhesive Energy
  58. 58. Prevention of Mold Invasion by Lignin/PCL Nanofibers S. An et al. Cellulose 24, 951-965 (2017).
  59. 59. Prevention of Mold Invasion by Lignin/PCL Nanofibers Photographs of the four molds tested, which correspond to Aspergillus versicola KUC5201, Cladosporium cladosporioides KUC1385, Penicillium brevicompactum KUC1819, and Trichoderma viride KUC5062, respectively.
  60. 60. Prevention of Mold Invasion by Lignin/PCL Nanofibers Photographs of the LPNM-wrapped specimens (a) at the beginning and (b) after two weeks of mold cultivation. (c) Optical image and (d, e) SEM images of the surface of the tested LPNM. The first, second, and third columns correspond to tdep = 3, 6, and 9 h cases, respectively.
  61. 61. Antibacterial (anti- E. coli) Action of Silver-Decorated Soy Protein Nanofibers Y. Zhang et al. Catalysis Communications 34, 35-40 (2013).
  62. 62. Heavy Metal Ion Adsorption on Nano-Textured Biopolymer Membranes A. Kolbasov, S. Sinha-Ray, A.L. Yarin, B. Pourdeyhimi. J. Membrane Sci. 530, 250-263 (2017).
  63. 63. Heavy Metal Ion Adsorption on Nano-Textured Biopolymer Membranes Macroscopic and microscopic images of: (a,b) lignin/nylon-6 membrane; (c,d) oats/nylon-6 membrane; (e,f) sodium alginate/PVA membrane; (g,h) soy protein/nylon-6 membrane; and (i,j) chitosan/nylon-6 membrane.
  64. 64. Lead Adsorption on Nano-Textured Biopolymer Membranes in Throughflow
  65. 65. Fiber-Size Distribution
  66. 66. Heavy Metal Adsorption on Biopolymer Nanofiber Membranes in Throughflow: Theory 2 2 c c c Pe Da c t x x ∂ ∂ ∂ + = − × θ ∂ ∂ ∂ (1) Da c t ∂θ =− × θ ∂ (2) where Pe and Da are the dimensionless Peclet and Damkohler numbers, respectively, v Pe D =  (3) 2 k Da D =  (4) The boundary conditions at t>0 are imposed as following c x 0, c 1; x 1, 0 x ∂ = = = = ∂ (5) The initial conditions at t=0 are imposed as c 1, 1= θ= (6)
  67. 67. Heavy Metal Adsorption on Biopolymer Nanofiber Membranes in Throughflow: Theory vs. Experiment (a,b) lignin- and (c,d) oats-containing nano-textured membranes.
  68. 68. Heavy Metal Adsorption on Commerical Adsorbents and Biopolymer Nanofiber Membranes: Comparative Efficiency Adsorbent Pb (mg/g) Price ($/Metric Ton) TiO2 81.3 1000-3000 Modified AlO3 100 ZnO 6.7 2000-2500 CeO2 9.2 Activated carbon 26.5 1000-2000 Lignin-containing nanofibers 37 Oat-containing nanofibers 11
  69. 69. Book Containing Multiple Details on Our Work Published by Cambridge University Press in 2014
  70. 70. Conclusion • Solution blowing is an economically feasible and industrially scalable method for producing nanofibers from bio-waste. • Mechanical and the adhesion characteristics are appropriate for a number of important applications. • Nanofibers can be formed from a wide range of plant- and animal-derived biopolymers. • Bio-waste-derived nano-textured membranes hold great promise for such biomedical applications as controlled drug delivery, protection of pruned plants from fungi invasion, protection of pine sapwood from mold invasion, and anti-bacterial action. • Nano-textured membranes solution blown from bio-waste hold great promise as adsorbents for removal of heavy metal ions from polluted water and are competitive with commercial adsorbents. • As by-products of biodiesel production and many other industrial processes, green nano-textured materials derived from bio-waste can dramatically increase sustainability. 70 University of Illinois at Chicago
  71. 71. Green nano-textured materials can become such great scorers as Pele! 71 University of Illinois at Chicago

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