EP3816327A1 - The formation method of porous antibacterial coatings on titanium and titanium alloys surface - Google Patents
The formation method of porous antibacterial coatings on titanium and titanium alloys surface Download PDFInfo
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- EP3816327A1 EP3816327A1 EP20460021.7A EP20460021A EP3816327A1 EP 3816327 A1 EP3816327 A1 EP 3816327A1 EP 20460021 A EP20460021 A EP 20460021A EP 3816327 A1 EP3816327 A1 EP 3816327A1
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/026—Anodisation with spark discharge
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/26—Anodisation of refractory metals or alloys based thereon
Definitions
- the subject of this invention is a formation method of the porous oxide layers on the surface of titanium and titanium alloys by plasma electrochemical oxidation. Due to the oxidation in baths containing suspended, insoluble particles of silver and copper compounds, the obtained oxide layers are intended to be characterized antimicrobial and/or bacteriostatic properties.
- Titanium and titanium alloys are used as long-term implant materials characterized by good biocompatibility with hard and soft tissue of the human body.
- bactericides such as antibiotics.
- a good example of different than antibiotics bactericides can be the modified implant biomaterials containing silver or copper in their composition. So far in the literature, there are known studies of obtaining layers containing silver or copper compounds formed from soluble forms of these elements compounds.
- the patent no. CN 101899700 describes the method of obtaining bioactive coatings on the surface of titanium and magnesium alloys by the plasma electrochemical oxidation using bath consisting of AgNO 3 , which results in the formation of porous oxide layers containing calcium, phosphorus and silver improving the bioactivity of the coatings, as well as their corrosion resistance and decreasing the risk of bacterial infections caused by implantation processes.
- the thickness of the coating formed on the surface of the titanium alloy measured 50-85 ⁇ m, the porosity of the coating was in the range from 20% to 30%, and the determined adhesion of the coating to the substrate was 23-40 MPa.
- the patent no. CN 108543109 describes the formation method of composite materials with antibacterial properties.
- the composite consists of ceramic TiO 2 and silver nanoparticles on the surface of a titanium alloy intended for use as the implant for bone tissue.
- a titanium alloy intended for use as the implant for bone tissue.
- Antibacterial properties of Ag (or Pt)-containing, calcium phosphate coatings formed by micro-arc oxidation W.H. Song, H.S. Ryu, S.H.
- Cimenoglu Materials Science and Engineering, 71 (2017) 565
- the method of plasma electrochemical oxidation using the bath containing Na 2 SiO 3 , NaOH and CH 3 COOAg presents the method of plasma electrochemical oxidation using the bath containing Na 2 SiO 3 , NaOH and CH 3 COOAg.
- Characteristics of multi-layer coatings synthesized on Ti6A14V alloy by micro-arc oxidation in silver nitrate added electrolytes F. Muhaffel, G. Cempura, M. Menekse, A. Czyrska-Filemonowicz, N. Karaguler, H. Cimenoglu, Surface and Coating Technology.
- Cimenoglu Materials Science and Engineering C, 48 (2015) 579
- Corrosion behaviour of Zn-incorporated antibacterial TiO2 porous coating on titanium (X. Zhang, H. Wang, J. Li, X. He, R. Hang, X. Huang, L. Tian, B.
- Chromium(VI) compounds, fluorides and orthophosphates are not used during the process, therefore air polluting products have been limited.
- microporous coating structures with good antibacterial properties, bioactivity, corrosion resistance and abrasion resistance are obtained.
- CN1035266261 there is presented the method of obtaining ceramic membranes containing zinc on the surface of titanium or magnesium modified by plasma electrochemical oxidation process using electrolytes containing soluble compounds of zinc and calcium, titanium or magnesium as anodes and stainless steel as cathode.
- the obtained ceramic membranes increase the bioactivity of the titanium or magnesium surface. Additionally, they degrade in the human body environment, causing the increase in immunity of human organism to bacterial infections and supporting the cell growth process in vitro.
- the titanium anodic oxidation method is described using the alkaline bath containing: 0.05 mol ⁇ dm -3 C 3 H 7 Na 2 O 6 P ⁇ 5H 2 O, 0.10 mol ⁇ dm -3 Ca(CH 3 COO) 2 ⁇ H 2 O and 0.04 mol ⁇ dm -3 Zn(CH 3 COO) 2 ⁇ 2H 2 O, as well as the acid bath containing: 85% H 3 PO 4 and 500 g of dissolved Zn(NO 3 ) 2 ⁇ 6H 2 O.
- the patent no. CN 107376897 describes the method of plasma oxidation of electrochemical titanium in the electrolyte containing zinc nanoparticles.
- Popat, P. Soares, "Thin Solid Films” presents the method of anodic electrochemical oxidation in the bath containing Ca(CH 3 COO) 2 , calcium glycerophosphate and Zn(CH 3 COO) 2 .
- the patent no. PL 225226 descibes the method of anodic electrochemical oxidation of tantalum, niobium and zirconium in the suspension of insoluble CaSiO 3 at a concentration of 1-300 g ⁇ dm -3 at the temperature of 15-50°C at the anodic current density of 5-200 mA ⁇ cm -2 and applied voltage of 100-650 V for 1-60 minutes.
- PL 225227 there is presented the method of electrochemical oxidation of plasma titanium and its alloys in a suspension of CaSiO 3 at a concentration of 1-300 g ⁇ dm -3 at the temperature of 15-50°C, at the anodic current density of 5-200 mA ⁇ cm -2 and applied voltage of 100-650 V in time 1-60 minutes.
- PL 396115 there is described the method of electrochemical oxidation of plasma titanium and its alloys in suspension containing ZrSiO 4 at the concentration of 1-100 g ⁇ dm -3 with the addition of the alkali metal hydroxide at the concentration of 5-100 g ⁇ dm -3 at the temperature of 15-50°C, at the anodic current density 5-500 mA ⁇ cm -2 and 1-600 V for 1-30 minutes.
- PL 214630 describes the method of electrochemical plasma oxidation of Ti-xNb-yZr alloys in the Ca(H 2 PO 2 ) 2 solution at the concentration of 1-150 g ⁇ dm -3 or in a NaH 2 PO 2 solution at a concentration of 1-250 g ⁇ dm -3 at the temperature of 15-50°C, at the anodic current density of 5-5000 mA ⁇ cm -2 and applied voltage of 100-650 V for 1-60 minutes.
- the aim of the invention is to develop a method allowing to obtain the porous oxide layers with incorporated compounds with antibacterial properties.
- the essence of the invention is the surface modification of titanium and titanium alloys via plasma electrochemical oxidation in the baths containing Ca(H 2 PO 2 ) 2 at a concentration from 0.01 mol ⁇ dm -3 to 5 mol ⁇ dm -3 , at the anodic current density from 1 mA ⁇ cm -2 to 250 mA ⁇ cm -2 and applied voltage from 50 V to 600 V.
- the surface-modified elements are immersed in an aqueous salt solution containing insoluble cooper(II) phosphate Cu 3 (PO 4 ) 2 , silver(I) phosphate Ag 3 PO 4 or zinc phosphate Zn 3 (PO 4 ) 2 at a concentration from 1 to 400 g ⁇ dm -3 .
- the invention describes the method of the plasma electrochemical oxidation of titanium and its titanium alloys in suspensions containing insoluble silver or copper compounds in the form of the oxides. In this way, it is possible to obtain porous oxide layers incorporated with particles of compounds characterised by the antibacterial properties.
- An addition of mentioned silver and copper suspension compounds can be a one-step modification of the surface of titanium and its alloys. Thanks to this, there is a chance to eliminate the necessity of high, oral antibiotic delivery route, which is the main cause of increasing bacteria resistance to antibiotics. Additionally, the number of side effects and allergic reactions related to antibiotic treatment can be reduced.
- the surfaces anodised via plasma electrolytic oxidation process are porous and rough, which promotes the proliferation of living cells and supports the osseointegration process.
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- Organic Chemistry (AREA)
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- Chemical Treatment Of Metals (AREA)
- Materials For Medical Uses (AREA)
Abstract
Description
- The subject of this invention is a formation method of the porous oxide layers on the surface of titanium and titanium alloys by plasma electrochemical oxidation. Due to the oxidation in baths containing suspended, insoluble particles of silver and copper compounds, the obtained oxide layers are intended to be characterized antimicrobial and/or bacteriostatic properties.
- Titanium and titanium alloys are used as long-term implant materials characterized by good biocompatibility with hard and soft tissue of the human body. During the implantation process, there is a risk of human tissues septic inflammation occurrence. Therefore, patients are being treated with bactericides such as antibiotics. However, because of the increasing resistance of bacteria to antibiotics, there are being carried out the studies of the alternative antibacterial agents. A good example of different than antibiotics bactericides can be the modified implant biomaterials containing silver or copper in their composition. So far in the literature, there are known studies of obtaining layers containing silver or copper compounds formed from soluble forms of these elements compounds.
- The patent no.
CN 101899700 describes the method of obtaining bioactive coatings on the surface of titanium and magnesium alloys by the plasma electrochemical oxidation using bath consisting of AgNO3, which results in the formation of porous oxide layers containing calcium, phosphorus and silver improving the bioactivity of the coatings, as well as their corrosion resistance and decreasing the risk of bacterial infections caused by implantation processes. The thickness of the coating formed on the surface of the titanium alloy measured 50-85 µm, the porosity of the coating was in the range from 20% to 30%, and the determined adhesion of the coating to the substrate was 23-40 MPa. The patent no.CN 108543109 describes the formation method of composite materials with antibacterial properties. The composite consists of ceramic TiO2 and silver nanoparticles on the surface of a titanium alloy intended for use as the implant for bone tissue. In the paper "Antibacterial properties of Ag (or Pt)-containing, calcium phosphate coatings formed by micro-arc oxidation" (W.H. Song, H.S. Ryu, S.H. Hong, Journal of Biomedical Materials Research Part A, 88 (1) (2009) 246) there is known the method of plasma electrochemical oxidation using the bath containing: 0.04 mol·dm-3 C3H7Na2O6P·5H2O, 0.40 mol·dm-3 (CH3COO)2Ca·H2O and AgNO3 or CH3COOAg in the concentration range 0.00003-0.00400 mol·dm-3 at 250-450 V. The manuscript "Antibacterial titanium surfaces for medical implants" (S. Ferraris, S. Spriano, Materials Science and Engineering, 61 (2016) 965) presents the method of plasma electrochemical oxidation using the bath containing 7-25 nm silver nanoparticles, (CH3COO)2Ca and calcium glycerophosphate. The paper "Fabrication of oxide layer on zirconium by micro-arc oxidation: Structural and antimicrobial characteristics" (S. Fidan, F. Muhaffel, M. Riool, G. Cempura, L. de Boer, S. A. J Zaat, A. Czyrska-Filemonowicz, H. Cimenoglu, Materials Science and Engineering, 71 (2017) 565) presents the method of plasma electrochemical oxidation using the bath containing Na2SiO3, NaOH and CH3COOAg. In the manuscript "Characteristics of multi-layer coatings synthesized on Ti6A14V alloy by micro-arc oxidation in silver nitrate added electrolytes" (F. Muhaffel, G. Cempura, M. Menekse, A. Czyrska-Filemonowicz, N. Karaguler, H. Cimenoglu, Surface and Coating Technology. 307 (2016) 308) there is known the method of plasma electrochemical oxidation in the bath containing Na2HPO4, Ca(CH3COO)2·H2O and AgNO3 in concentrations 0.1 g·dm-3 or 0.4 g·dm-3. In the manuscript "Corrosion Resistance and Antibacterial Properties of Ag-Containing MAO Coatings on AZ31 Magnesium Alloy Formed by Microarc Oxidation" (S. Ryu, SH Hong, Journal of Electrochemical Society, 157 (2010) 131), the method of plasma electrochemical oxidation in bath containing Na2SiO3 and AgNO3 is known. The paper "High-current anodization: A novel strategy to functionalize titanium-based biomaterials" (C. Chang, X. Huang, Y. Liu, L. Bai, X. Yang, R. Hang, B. Tang, PK Chu, Electrochimica Acta, 173 (2015) 345) presents the method of plasma electrochemical oxidation in the bath containing 7.6 g·dm-3 Na3PO4, 9.4 g·dm-3 Ca(NO3)2 and 1.0 g·dm-3 AgNO3. The publication "In vitro antibacterial activity of porous TiO2-Ag composite layers against methicillin-resistant Staphylococcus ureus" (B.S. Necula, L.E. Fratila-Apachitei, S.A. Zaat, I. Apachitei, J. Duszczyk, Acta Biomaterialia, 5 (2009) 3573) presents the method of plasma electrochemical oxidation in the bath containing 0.15 mol·dm-3 Ca(CH3COO)2 or 0.02 mol·dm-3 calcium glycerophosphate with the addition of 0.03 g·dm-3 of nanoparticles Ag. The manuscript "Characteristics of multi-layer coating formed on commercially pure titanium for biomedical applications" (D. Teker, F. Muhaffel, M. Menekse, NG Karaguler, M. Baydogan, H. Cimenoglu, Materials Science and Engineering C, 48 (2015) 579) presents the method of anodic electrochemical oxidation using the bath containing Na2HPO4, Ca(CH3COO)2 and 0.0025 mol·dm-3 CH3COOAg. In the paper "Corrosion behaviour of Zn-incorporated antibacterial TiO2 porous coating on titanium" (X. Zhang, H. Wang, J. Li, X. He, R. Hang, X. Huang, L. Tian, B. Tang, Ceramic International, 32 (2016) 919) there is presented the method of anodic electrochemical oxidation in the bath consisting of 0.02 mol·dm-3 sodium β-glycerophosphate, 0.1 mol·dm-3 Ca(CH3COO)2, 0.1 mol·dm-3 Zn(CH3COO)2 and 6 g·dm-3 of nanoparticles Ag. In the manuscript "Energy-Dispersive X-Ray Spectroscopy Mapping of Porous Coatings Obtained on Titanium by Plasma Electrolytic Oxidation in a Solution Containing Concentrated Phosphoric Acid with Copper Nitrate" (K. Rokosz, T. Hryniewicz, L. Dudek, A. Schutz, J. Heeg and M. Wienecke, Advances in Materials Science, 16 (2016) 15) there is presented the method of anodic oxidation of titanium using the bath containing Cu(NO3)2. 1 dm3 of bath may contain 85% H3PO4 and 600 g of dissolved Cu(NO3)2. The process can be carried out at 450 V. In the work "Catalytically active cobalt-copper-oxide layers on aluminium and titanium" (I.V. Lukiyanchuk, I.V. Chernykh, V.S. Rudnev, A. Yu Ustinov, L.M. Tyrina, P.M. Nedozorov, E.E. Dmitrieva, Protection of Metals and Physical Chemistry of Surfaces, 50 (2014) 209) there is known the method of obtaining oxide layers on the titanium surface by the plasma electrolytic oxidation treatment, followed by the modification of the obtained oxide layers with copper and cobalt by impregnation in solutions of soluble copper and cobalt salts. The manuscript "Biological Activity and Antibacterial Property of Nano-structured TiO2 Coating Incorporated with Cu Prepared by Micro-arc Oxidation" (W. Zhu, Z. Zhang, B. Gu, J. Sun, L. Zhu, Journal of Materials Science & Technology, 29 (2013) 237) describes the plasma electrochemical oxidation method using the bath containing 0.05 mol·dm-3 sodium β-glycerophosphate, 0.1 mol·dm-3 Ca(CH3COO)2 and 0.05 mol·dm-3 (CH3COO)2Cu. The publication "SEM, EDS and XPS Analysis of the Coatings · Obtained on Titanium after Plasma Electrolytic Oxidation in Electrolytes Containing Copper Nitrate" (K. Rokosz, T. Hryniewicz, D. Matýsek, S. Raaen, J. Valíček, L. Dudek, M. Harničárová, Materials, 9 (2016) 318) there is known the method of anodic oxidation of titanium from the bath containing Cu(NO3)2. 1 dm3 of bath may contain 85% H3PO4 and 10-600 g of dissolved Cu(NO3)2. In the paper "Microstructure and antibacterial properties of Cu-doped TiO2 coating on titanium by micro-arc oxidation" (X. Yao, X. Zhang, H. Wu, L. Tian, Y. Ma, B. Tang, Applied Surface Science, 292 (2014) 944) there is known the method of plasma electrochemical oxidation in the bath containing 2 g·dff-3 NaOH, 15 g·dm-3 NaH2PO4 and 3 g·dm-3 Cu nanoparticles. In the manuscript "One-step fabrication of cytocompatible micro/nano-textured surface with TiO2 mesoporous arrays on titanium by high current anodization" (X. Huang, Y. Liu, H. Yu, X. Yang, Y. Wang, R. Hang, B. Tang, Electrochimica Acta, 199 (2016) 116) there is known the method of anodic electrochemical oxidation using the bath containing 3.8-7.6 g·dm-3 Na3PO4 and 1.0-8.0 g·dm-3 Cu(NO3)2. The paper "The dual function of Cu-doped TiO2 coatings on titanium for application in percutaneous implants" (L. Zhang, J. Guo, X. Huang, Y. Zhang, Y. Han, Journal of Materials Chemistry, 4 (2016) 3788) presents the method of anodic electrochemical oxidation using the bath containing 0.02 mol·dm-3 sodium β-glycerophosphate, 0.02 mol-dm-3 Ca(CH3COO)2 and 0.00125-0.005 mol·dm-3 Cu(CH3COO)2. The patent no.CN103911644 describes the plasma electrochemical oxidation of titanium alloys using baths containing phytic acid or phytate with the addition of electrolytes such as bioactive calcium, magnesium, zinc salts or with the addition of organic compounds such as tannic acid or hydroxides. Chromium(VI) compounds, fluorides and orthophosphates are not used during the process, therefore air polluting products have been limited. As a result of the process, microporous coating structures with good antibacterial properties, bioactivity, corrosion resistance and abrasion resistance are obtained. In the patent no. there is presented the method of obtaining ceramic membranes containing zinc on the surface of titanium or magnesium modified by plasma electrochemical oxidation process using electrolytes containing soluble compounds of zinc and calcium, titanium or magnesium as anodes and stainless steel as cathode. The obtained ceramic membranes increase the bioactivity of the titanium or magnesium surface. Additionally, they degrade in the human body environment, causing the increase in immunity of human organism to bacterial infections and supporting the cell growth process in vitro. In the publication "Antibacterial activity and increased bone marrow stem cell functions of Zn-incorporated TiO2 coatings on titanium" (H. Hu, W. Zhang, Y. Qiao, X. Jiang, X. Liu, C. Ding, "Acta Biomaterialia" (8 (2012) 904) there is known the method of plasma electrochemical oxidation of titanium using the baths containing zinc. The bath containing 0.1 mol·dm-3 C4H6O4Ca·H2O,CN1035266261
0.05 mol·dm-3 C3H7Na2O6P·5H2O and Zn(CH3COO)2·2H2O in the concentration range 0.02-0.06 mol·dm-3 has been used. In the paper "SEM and EDS Characterization of Porous Coatings Obtained On Titanium by Plasma Electrolytic Oxidation in Electrolyte Containing Concentrated Phosphoric Acid with Zinc Nitrate" (K. Rokosz, T. Hryniewicz, K. Pietrzak, W. Malorny, "Advances in Materials Science" (17 (2017) 41), the titanium anodic oxidation method is described using the alkaline bath containing: 0.05 mol·dm-3 C3H7Na2O6P·5H2O, 0.10 mol·dm-3 Ca(CH3COO)2·H2O and 0.04 mol·dm-3 Zn(CH3COO)2·2H2O, as well as the acid bath containing: 85% H3PO4 and 500 g of dissolved Zn(NO3)2·6H2O. The patent no.CN 107376897 describes the method of plasma oxidation of electrochemical titanium in the electrolyte containing zinc nanoparticles. In the manuscript "Preparation and photocatalytic performance of ZnO/WO3/TiO2 composite coatings formed by plasma electrolytic oxidation" (Q. Honglei, L. Chen, Y. Xiwen, W. Mingyue, Y. Zongcheng, "Journal of Materials Science: Materials in Electronics "(29 (2018) 2060) there is known the method of plasma oxidation of electrochemical titanium in the electrolyte containing zinc nanoparticles. In the paper "Enhanced corrosion resistance and in-vitro biodegradation of plasma electrolytic oxidation coatings prepared on AZ91 Mg alloy using ZnO nanoparticles-incorporated electrolyte" (A. Bordbar-Khiabani, B. Yarmand, M. Mozafari, Surface and Coatings Technology (360 (2019) 153) there is described the method of plasma electrochemical oxidation in the bath containing 4.5 g·dm-3 of ZnO nanoparticles. In the manuscript "The effect of applied voltages on the structure, apatite-inducing ability and antibacterial ability of micro arc oxidation coating formed on titanium Surface" (Q. Du, D. Wei, Y. Wang, S. Cheng, S. Liu, Y. Zhou, D. Jia, Bioactive Materials (3 (2018) 426) there is presented the method of plasma electrochemical oxidation using the bath consisting of 15 g·dm-3 EDTA, 8.8 g·dm-3 Ca(CH3COO)2·H2O, 6.3 g·dm-3 Ca(H2PO4)2·H2O, 7.1 g·dm-3 Na2SiO3·9H2O, 5 g·dm-3 NaOH, 6 mL·dm-3 H2O2 and 8.5 g·dm-3 Zn(CH3COO)2. The publication "Bactericidal activity and cytotoxicity of a zinc doped PEO titanium coating" (L. Sopchenski, K. Popat, P. Soares, "Thin Solid Films" (660 (2018) 477) presents the method of anodic electrochemical oxidation in the bath containing Ca(CH3COO)2, calcium glycerophosphate and Zn(CH3COO)2. The patent no. descibes the method of anodic electrochemical oxidation of tantalum, niobium and zirconium in the suspension of insoluble CaSiO3 at a concentration of 1-300 g·dm-3 at the temperature of 15-50°C at the anodic current density of 5-200 mA·cm-2 and applied voltage of 100-650 V for 1-60 minutes. In the patent no.PL 225226 there is presented the method of electrochemical oxidation of plasma titanium and its alloys in a suspension of CaSiO3 at a concentration of 1-300 g·dm-3 at the temperature of 15-50°C, at the anodic current density of 5-200 mA·cm-2 and applied voltage of 100-650 V in time 1-60 minutes. In the patent no.PL 225227 there is described the method of electrochemical oxidation of plasma titanium and its alloys in suspension containing ZrSiO4 at the concentration of 1-100 g·dm-3 with the addition of the alkali metal hydroxide at the concentration of 5-100 g·dm-3 at the temperature of 15-50°C, at the anodic current density 5-500 mA·cm-2 and 1-600 V for 1-30 minutes. The patent no.PL 396115 describes the method of electrochemical plasma oxidation of Ti-xNb-yZr alloys in the Ca(H2PO2)2 solution at the concentration of 1-150 g·dm-3 or in a NaH2PO2 solution at a concentration of 1-250 g·dm-3 at the temperature of 15-50°C, at the anodic current density of 5-5000 mA·cm-2 and applied voltage of 100-650 V for 1-60 minutes.PL 214630 - The aim of the invention is to develop a method allowing to obtain the porous oxide layers with incorporated compounds with antibacterial properties.
- The essence of the invention is the surface modification of titanium and titanium alloys via plasma electrochemical oxidation in the baths containing Ca(H2PO2)2 at a concentration from 0.01 mol·dm-3 to 5 mol·dm-3, at the anodic current density from 1 mA·cm-2 to 250 mA·cm-2 and applied voltage from 50 V to 600 V. The surface-modified elements are immersed in an aqueous salt solution containing insoluble cooper(II) phosphate Cu3(PO4)2, silver(I) phosphate Ag3PO4 or zinc phosphate Zn3(PO4)2 at a concentration from 1 to 400 g·dm-3.
- The invention describes the method of the plasma electrochemical oxidation of titanium and its titanium alloys in suspensions containing insoluble silver or copper compounds in the form of the oxides. In this way, it is possible to obtain porous oxide layers incorporated with particles of compounds characterised by the antibacterial properties. An addition of mentioned silver and copper suspension compounds can be a one-step modification of the surface of titanium and its alloys. Thanks to this, there is a chance to eliminate the necessity of high, oral antibiotic delivery route, which is the main cause of increasing bacteria resistance to antibiotics. Additionally, the number of side effects and allergic reactions related to antibiotic treatment can be reduced. The surfaces anodised via plasma electrolytic oxidation process are porous and rough, which promotes the proliferation of living cells and supports the osseointegration process.
- Example I: The titanium implant, pre-treated by polishing, degreasing, etching and rinsing in demineralised water is placed in the solution containing 0.1 mol·dm-3 Ca(H2PO2)2 and the suspension of 10 g·dm-3 Ag3PO4. After placing the implant in the anodising bath, the electrolytic plasma oxidation process is carried out by polarizing it with the anodic current density of 150 mA·cm-2. The process is carried out for 5 minutes, with the maximum voltage of 300 V. After the process, the implant is rinsed in demineralised water and air-dried at 45°C.
- Example II: The implant made of Ti-13Nb-13Zr alloy, mechanically pre-treated, degreased, etched and rinsed in demineralised water is placed in the anodising bath containing 0.01 mol·dm-3 Ca(H2PO2)2 and the suspension of 100 g·dm-3 Cu3(PO4)2. After placing the implant in the bath, the electrolytic plasma oxidation process is carried out by polarizing it with the anodic current density of 100 mA·cm-2. The process is carried out for 7 minutes, with the maximum voltage of 350 V. After the process, the implant is rinsed in demineralised water and air-dried at 45°C.
- Example III: The implant made of Ti-15Mo alloy, mechanically pre-treated, degreased, etched and rinsed in demineralised water is placed in the anodising bath containing 5 mol·dm-3 Ca(H2PO2)2 and the suspension of 200 g·dm-3 Zn3(PO4)2. After placing the implant in the bath, the electrolytic plasma oxidation process is carried out by polarizing it with the anodic current density of 200 mA·cm-2. The process is carried out for 5 minutes, with the maximum voltage of 400 V. After the process, the implant is rinsed in demineralised water and air-dried at 45°C.
Claims (4)
- The method of titanium surface modification by plasma electrochemical oxidation in Ca(H2PO2)2 baths at a concentration from 0.01 mol·dm-3 to 5 mol·dm-3 with an anodic current density from 1 mA·cm-2 to 250 mA·cm-2 and applied voltage from 50 V to 600 V is characterized by immersing the surface-modified element in an aqueous salt solution with insoluble particles of metal phosphate at a concentration from 1 g·dm-3 to 400 g·dm-3.
- According to patent claim 1, the process is characteristic because the aqueous salt solution contains copper(II) phosphate Cu3(PO4)2 at a concentration from 1 g·dm-3 to 400 g·dm-3.
- According to patent claim 1, the process is characteristic because the aqueous salt solution contains silver(I) phosphate Ag3PO4 at a concentration from 1 g·dm-3 to 400 g·dm-3.
- According to patent claim 1, the process is characteristic because the aqueous salt solution contains zinc phosphate Zn3(PO4)2 at a concentration from 1 g·dm-3 to 400 g·dm-3.
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| PL430374A PL239584B1 (en) | 2019-06-25 | 2019-06-25 | Method of obtaining porous antibacterial coatings on the surface of titanium and its alloys |
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| EP3816327A1 true EP3816327A1 (en) | 2021-05-05 |
| EP3816327B1 EP3816327B1 (en) | 2023-10-18 |
| EP3816327B8 EP3816327B8 (en) | 2023-12-20 |
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Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL225226A1 (en) | 1980-06-26 | 1982-01-04 | Zaklady Wytworcze Urzadzen Syg | |
| PL225227A1 (en) | 1980-06-26 | 1982-01-04 | Ct Kt Maszyn Gorniczych Komag | |
| RU94028190A (en) * | 1994-07-27 | 1996-05-20 | Институт химии Дальневосточного отделения РАН | Electrolyte for titanium and its alloys microarc oxidation |
| CN101899700A (en) | 2009-05-25 | 2010-12-01 | 佳木斯大学 | Preparation method of silver-loaded antibacterial bioactive coating on magnesium and titanium surfaces by ultrasonic micro-arc oxidation |
| CN102677125A (en) * | 2012-06-13 | 2012-09-19 | 西北有色金属研究院 | Preparation method of active antibacterial composite coating on surface of titanium and titanium alloy medical instrument |
| PL396115A1 (en) | 2011-08-29 | 2013-03-04 | Politechnika Slaska | Method for anodic passivation of the vanadium-free titanium Ti-xNb-yZr alloys |
| PL214630B1 (en) | 2010-03-22 | 2013-08-30 | Politechnika Slaska Im Wincent | Method for modification of the surface layer of Ti-xNb-yZr alloys with calcium and phosphorus by electrochemical plasma oxidation |
| PL214958B1 (en) * | 2010-03-22 | 2013-10-31 | Politechnika Slaska Im Wincent | Method for modification of the surface layer of titanium and its alloys with calcium and phosphorus by electrochemical plasma oxidation |
| CN103526261A (en) | 2013-10-17 | 2014-01-22 | 赵全明 | Preparation method of zinc-containing micro-arc oxidation electrolyte and zinc-containing biological ceramic membrane |
| CN103911644A (en) | 2014-04-09 | 2014-07-09 | 江西科技师范大学 | Micro-arc oxidation electrolyte and micro-arc oxidation method for titanium alloys |
| CN107376897A (en) | 2017-06-27 | 2017-11-24 | 华南理工大学 | A kind of oxidation catalysis film containing three metals and preparation method and application |
| CN108543109A (en) | 2018-03-13 | 2018-09-18 | 淮阴工学院 | It is low to grind dual antibacterial titanium-based nano composite material bone implant and its manufacturing process |
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Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL225226A1 (en) | 1980-06-26 | 1982-01-04 | Zaklady Wytworcze Urzadzen Syg | |
| PL225227A1 (en) | 1980-06-26 | 1982-01-04 | Ct Kt Maszyn Gorniczych Komag | |
| RU94028190A (en) * | 1994-07-27 | 1996-05-20 | Институт химии Дальневосточного отделения РАН | Electrolyte for titanium and its alloys microarc oxidation |
| CN101899700A (en) | 2009-05-25 | 2010-12-01 | 佳木斯大学 | Preparation method of silver-loaded antibacterial bioactive coating on magnesium and titanium surfaces by ultrasonic micro-arc oxidation |
| PL214630B1 (en) | 2010-03-22 | 2013-08-30 | Politechnika Slaska Im Wincent | Method for modification of the surface layer of Ti-xNb-yZr alloys with calcium and phosphorus by electrochemical plasma oxidation |
| PL214958B1 (en) * | 2010-03-22 | 2013-10-31 | Politechnika Slaska Im Wincent | Method for modification of the surface layer of titanium and its alloys with calcium and phosphorus by electrochemical plasma oxidation |
| PL396115A1 (en) | 2011-08-29 | 2013-03-04 | Politechnika Slaska | Method for anodic passivation of the vanadium-free titanium Ti-xNb-yZr alloys |
| CN102677125A (en) * | 2012-06-13 | 2012-09-19 | 西北有色金属研究院 | Preparation method of active antibacterial composite coating on surface of titanium and titanium alloy medical instrument |
| CN103526261A (en) | 2013-10-17 | 2014-01-22 | 赵全明 | Preparation method of zinc-containing micro-arc oxidation electrolyte and zinc-containing biological ceramic membrane |
| CN103911644A (en) | 2014-04-09 | 2014-07-09 | 江西科技师范大学 | Micro-arc oxidation electrolyte and micro-arc oxidation method for titanium alloys |
| CN107376897A (en) | 2017-06-27 | 2017-11-24 | 华南理工大学 | A kind of oxidation catalysis film containing three metals and preparation method and application |
| CN108543109A (en) | 2018-03-13 | 2018-09-18 | 淮阴工学院 | It is low to grind dual antibacterial titanium-based nano composite material bone implant and its manufacturing process |
Non-Patent Citations (26)
| Title |
|---|
| A. BORDBAR-KHIABANIB. YARMANDM. MOZAFARI: "Enhanced corrosion resistance and in-vitro biodegradation of plasma electrolytic oxidation coatings prepared on AZ91 Mg alloy using ZnO nanoparticles-incorporated electrolyte", SURFACE AND COATINGS TECHNOLOGY, vol. 360, 2019, pages 153 |
| B.S. NECULAL.E. FRATILA-APACHITEIS.A. ZAATI. APACHITEIJ. DUSZCZYK: "In vitro antibacterial activity of porous Ti0 -Ag composite layers against methicillin-resistant Staphylococcus ureus", ACTA BIOMATERIALIA, vol. 5, 2009, pages 3573, XP026693830, DOI: 10.1016/j.actbio.2009.05.010 |
| C. CHANGX. HUANGY. LIUL. BAIX. YANGR. HANGB. TANGPK CHU: "High-current anodization: A novel strategy to functionalize titanium-based biomaterials", ELECTROCHIMICA ACTA, vol. 173, 2015, pages 345, XP029209963, DOI: 10.1016/j.electacta.2015.05.075 |
| D. TEKERF. MUHAFFELM. MENEKSENG KARAGULERM. BAYDOGANH. CIMENOGLU: "Characteristics of multi-layer coating formed on commercially pure titanium for biomedical applications", MATERIALS SCIENCE AND ENGINEERING C, vol. 48, 2015, pages 579 |
| DATABASE EPODOC [online] EUROPEAN PATENT OFFICE, THE HAGUE, NL; 20 May 1996 (1996-05-20), XP002800828, Database accession no. RU-94028190-A * |
| F. MUHAFFELG. CEMPURAM. MENEKSEA. CZYRSKA-FILEMONOWICZN. KARAGULERH. CIMENOGLU: "Characteristics of multi-layer coatings synthesized on Ti6Al4V alloy by micro-arc oxidation in silver nitrate added electrolytes", SURFACE AND COATING TECHNOLOGY, vol. 307, 2016, pages 308, XP029823815, DOI: 10.1016/j.surfcoat.2016.09.002 |
| H. HUW. ZHANGY. QIAOX. JIANGX. LIUC. DING: "Antibacterial activity and increased bone marrow stem cell functions of Zn-incorporated TiOz coatings on titanium", ACTA BIOMATERIALIA, vol. 8, 2012, pages 904 |
| I.V. LUKIYANCHUKI.V. CHERNYKHV.S. RUDNEVA. YU USTINOVL.M. TYRINAP.M. NEDOZOROVE.E. DMITRIEVA: "Catalytically active cobalt-copper-oxide layers on aluminium and titanium", PROTECTION OF METALS AND PHYSICAL CHEMISTRY OF SURFACES, vol. 50, 2014, pages 209 |
| K. ROKOSZT. HRYNIEWICZD. MATYSEKS. RAAENJ. VALICEKL. DUDEKM. HARNICAROVA: "SEM, EDS and XPS Analysis of the Coatings , Obtained on Titanium after Plasma Electrolytic Oxidation in Electrolytes Containing Copper Nitrate", MATERIALS, vol. 9, 2016, pages 318 |
| K. ROKOSZT. HRYNIEWICZK. PIETRZAKW. MALORNY: "SEM and EDS Characterization of Porous Coatings Obtained On Titanium by Plasma Electrolytic Oxidation in Electrolyte Containing Concentrated Phosphoric Acid with Zinc Nitrate", ADVANCES IN MATERIALS SCIENCE, vol. 17, 2017, pages 41 |
| K. ROKOSZT. HRYNIEWICZL. DUDEKA. SCHUTZJ. HEEGM. WIENECKE: "Energy-Dispersive X-Ray Spectroscopy Mapping of Porous Coatings Obtained on Titanium by Plasma Electrolytic Oxidation in a Solution Containing Concentrated Phosphoric Acid with Copper Nitrate", ADVANCES IN MATERIALS SCIENCE, vol. 16, 2016, pages 15 |
| KAZEK-KESIK ALICJA ET AL: "Surface characterisation of Ti-15Mo alloy modified by a PEO process in various suspens", MATERIALS SCIENCE AND ENGINEERING C, vol. 39, 12 March 2014 (2014-03-12), pages 259 - 272, XP029029210, ISSN: 0928-4931, DOI: 10.1016/J.MSEC.2014.03.008 * |
| L. SOPCHENSKIK. POPATP. SOARES: "Bactericidal activity and cytotoxicity of a zinc doped PEO titanium coating", THIN SOLID FILMS, vol. 660, 2018, pages 477, XP085440169, DOI: 10.1016/j.tsf.2018.05.055 |
| L. ZHANGJ. GUOX. HUANGY. ZHANGY. HAN: "The dual function of Cu-doped Ti02 coatings on titanium for application in percutaneous implants", JOURNAL OF MATERIALS CHEMISTRY, vol. 4, 2016, pages 3788 |
| MUHAFFEL FAIZ ET AL: "Characteristics of multi-layer coatings synthesized on Ti6Al4V alloy by micro-arc oxidation in silver nitrate added electrolytes", SURFACE AND COATINGS TECHNOLOGY, ELSEVIER BV, AMSTERDAM, NL, vol. 307, 1 September 2016 (2016-09-01), pages 308 - 315, XP029823815, ISSN: 0257-8972, DOI: 10.1016/J.SURFCOAT.2016.09.002 * |
| NECULA B S ET AL: "In vitro antibacterial activity of porous TiO"2-Ag composite layers against methicillin-resistant Staphylococcus aureus", ACTA BIOMATERIALIA, ELSEVIER, AMSTERDAM, NL, vol. 5, no. 9, 1 November 2009 (2009-11-01), pages 3573 - 3580, XP026693830, ISSN: 1742-7061, [retrieved on 20090518], DOI: 10.1016/J.ACTBIO.2009.05.010 * |
| Q. DUD. WEIY. WANGS. CHENGS. LIUY. ZHOUD. JIA: "The effect of applied voltages on the structure, apatite-inducing ability and antibacterial ability of micro arc oxidation coating formed on titanium Surface", BIOACTIVE MATERIALS, vol. 3, 2018, pages 426 |
| Q. HONGLEIL. CHENY. XIWENW. MINGYUEY. ZONGCHENG: "Preparation and photocatalytic performance of Zn0/WO /Ti02 composite coatings formed by plasma electrolytic oxidation", JOURNAL OF MATERIALS SCIENCE: MATERIALS IN ELECTRONICS, vol. 29, 2018, pages 2060 |
| S. FERRARISS. SPRIANO: "Antibacterial titanium surfaces for medical implants", MATERIALS SCIENCE AND ENGINEERING, vol. 61, 2016, pages 965 |
| S. FIDANF. MUHAFFELM. RIOOLG. CEMPURAL. DE BOERS. A. J ZAATA. CZYRSKA-FILEMONOWICZH. CIMENOGLU: "Fabrication of oxide layer on zirconium by micro-arc oxidation: Structural and antimicrobial characteristics", MATERIALS SCIENCE AND ENGINEERING, vol. 71, 2017, pages 565 |
| S. RYUSH HONG: "Corrosion Resistance and Antibacterial Properties of Ag-Containing MAO Coatings on AZ31 Magnesium Alloy Formed by Microarc Oxidation", JOURNAL OF ELECTROCHEMICAL SOCIETY, vol. 157, 2010, pages 131 |
| W. ZHUZ. ZHANGB. GUJ. SUNL. ZHU: "Biological Activity and Antibacterial Property of Nano-structured Ti0 Coating Incorporated with Cu Prepared by Micro-arc Oxidation", JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY, vol. 29, 2013, pages 237 |
| W.H. SONGH.S. RYUS.H. HONG: "Antibacterial properties of Ag (or Pt)-containing , calcium phosphate coatings formed by micro-arc oxidation", JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, vol. 88, no. 1, 2009, pages 246 |
| X. HUANGY. LIUH. YUX. YANGY. WANGR. HANGB. TANG: "One-step fabrication of cytocompatible micro/nano-textured surface with Ti0 mesoporous arrays on titanium by high current anodization", ELECTROCHIMICA ACTA, vol. 199, 2016, pages 116, XP029510966, DOI: 10.1016/j.electacta.2016.03.119 |
| X. YAOX. ZHANGH. WUL. TIANY. MAB. TANG: "Microstructure and antibacterial properties of Cu-doped Ti0 coating on titanium by micro-arc oxidation", APPLIED SURFACE SCIENCE, vol. 292, 2014, pages 944 |
| X. ZHANGH. WANGJ. LIX. HER. HANGX. HUANGL. TIANB. TANG: "Corrosion behaviour of Zn-incorporated antibacterial Ti02 porous coating on titanium", CERAMIC INTERNATIONAL, vol. 32, 2016, pages 919 |
Also Published As
| Publication number | Publication date |
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| EP3816327B1 (en) | 2023-10-18 |
| PL3816327T3 (en) | 2024-03-18 |
| PL430374A1 (en) | 2020-07-13 |
| PL239584B1 (en) | 2021-12-20 |
| EP3816327B8 (en) | 2023-12-20 |
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