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Fabrication of superhydrophobic TA2 titanium alloy and preliminary assessment of its antifouling, self-cleaning, anti-icing, friction resistance, and corrosion resistance performance 超疏水 TA2 钛合金的制造及其防污、自清洁、防结冰、耐摩擦和耐腐蚀性能的初步评估
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-03-01 DOI: 10.1007/s11998-023-00900-5
Sian Chen, Benfeng Zhu, Xuesheng Wang, Na Chen, Guowei Ji, Mengyan Liu, Yumeng Yang, Li Ren, Shuxin Shuai, Jiajun Cao, Li Jiang, Guoying Wei

Titanium alloy-based superhydrophobic surfaces have great advantages in terms of self-cleaning and corrosion resistance. To extend the application of titanium alloy, a multifunctional superhydrophobic TA2 titanium alloy was fabricated by anodic oxidation and chemical modification. Regular TiO2 nanotube arrays were obtained after anodic oxidation and completely covered by 1H,1H,2H,2H-perfluorodecyltriethoxysilane. The water contact angle of superhydrophobic TA2 titanium alloy is as high as 153.4° ± 0.6°, and the contact angle of the surface shows good stability in different pH aqueous solutions and different concentrations of NaCl solutions. At −10 °C, the icing time of superhydrophobic TA2 titanium alloy surface can be extended to 4400 s. Furthermore, the superhydrophobic TA2 titanium alloy still maintains superhydrophobic properties when polished 70 times by sandpaper, indicating that the surface has good friction resistance. Electrochemical impedance spectroscopy results show that superhydrophobic TA2 titanium alloy with a Z′|f=0.01 Hz value of 84 kΩ cm2 has better corrosion resistance compared with the TA2 titanium alloy. These results indicate that the superhydrophobic composite film integrates multiple functions on the surface of TA2 titanium alloy, which greatly expands its application.

钛合金基超疏水表面在自清洁和耐腐蚀方面具有很大优势。为了扩大钛合金的应用范围,研究人员通过阳极氧化和化学修饰制备了多功能超疏水 TA2 钛合金。阳极氧化后得到规则的 TiO2 纳米管阵列,并被 1H,1H,2H,2H-全氟癸基三乙氧基硅烷完全覆盖。超疏水 TA2 钛合金的水接触角高达 153.4° ± 0.6°,在不同 pH 值的水溶液和不同浓度的氯化钠溶液中,其表面接触角均表现出良好的稳定性。此外,超疏水 TA2 钛合金在用砂纸抛光 70 次后仍能保持超疏水特性,表明其表面具有良好的耐摩擦性。电化学阻抗谱结果表明,与 TA2 钛合金相比,Z′|f=0.01 Hz 值为 84 kΩ cm2 的超疏水 TA2 钛合金具有更好的耐腐蚀性。这些结果表明,超疏水复合膜在 TA2 钛合金表面集成了多种功能,大大拓展了其应用范围。
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引用次数: 0
Preparation and application of fluorine-containing acrylate emulsion in two-component waterborne polyurethane coatings 双组分水性聚氨酯涂料中含氟丙烯酸酯乳液的制备和应用
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-28 DOI: 10.1007/s11998-023-00893-1
Aohuan Guo, Jianben Xu, Caili Yu, Faai Zhang

Traditional two-component waterborne polyurethane (2K WPU) has low water resistance, which limits its application in the wide field. In this work, fluorine-modified 2K WPU films (2K-WFPUs) were successfully prepared using a fluorine-modified acrylate emulsion as hydroxyl component and a hydrophilically modified polyisocyanate as curing agent. Fourier transform infrared spectroscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy analysis indicate that hexafluorobutyl acrylate (HFBA) was successfully introduced into the 2K-WFPUs. The effects of HFBA content on the surface, thermal stability, water resistance, mechanical, and application properties of 2K-WFPUs were investigated. Compared with the unmodified film, with the increase in HFBA level from 0 to 8%, the static water contact angle of 2K-WFPUs increased from 66° to 92°, the surface-free energy decreased from 42.7 to 28.4 mJ m−2, the water absorption reduced from 15.9 to 9.9%. Thermogravimetric analysis shows that the thermal stabilities of 2K-WFPUs were improved remarkably. Meanwhile, adding HFBA did not weaken the impact resistance, flexibility, and adhesion of 2K-WFPUs and maintained the highest level. The fluorine-modified 2K WPU coatings have potential application in wood furniture and automotive finishing.

Graphical abstract

传统的双组分水性聚氨酯(2K WPU)耐水性较低,限制了其在广泛领域的应用。本研究以氟改性丙烯酸酯乳液为羟基组分,亲水改性多异氰酸酯为固化剂,成功制备了氟改性 2K 水性聚氨酯薄膜(2K-WFPUs)。傅立叶变换红外光谱、扫描电子显微镜和 X 射线光电子能谱分析表明,六氟丁基丙烯酸酯(HFBA)被成功引入到 2K-WFPU 中。研究了 HFBA 含量对 2K-WFPU 表面、热稳定性、耐水性、机械和应用性能的影响。与未改性薄膜相比,随着 HFBA 含量从 0% 增加到 8%,2K-WFPU 的静态水接触角从 66°增加到 92°,表面自由能从 42.7 mJ m-2 降低到 28.4 mJ m-2,吸水率从 15.9% 降低到 9.9%。热重分析表明,2K-WFPU 的热稳定性显著提高。同时,添加 HFBA 不会削弱 2K-WFPU 的抗冲击性、柔韧性和粘附性,并保持了最高水平。氟改性 2K WPU 涂料有望应用于木制家具和汽车涂装。
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引用次数: 0
Tuning the mechanical properties of epoxy-acrylate core–shell nanostructured film via epoxy concentration in the core layer 通过芯层中的环氧浓度调节环氧-丙烯酸酯芯壳纳米结构薄膜的机械性能
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-26 DOI: 10.1007/s11998-023-00888-y
Eyann Lee, Zulkifli Mohamad Ariff, Mohamad Danial Shafiq, Raa Khimi Shuib, Muhamad Sharan Musa

Epoxy-acrylate (EA) core–shell nanoparticles have gained significant attention recently due to their dual unique properties as heterogeneous materials, particularly in coating applications. However, the effect of epoxy (EP) concentration in core layer on mechanical properties is still limited, and the mechanism of how it affects the film's performance is not well understood. In this study, we investigate the effect of varying EP concentration in the core layer on the mechanical properties of nanostructured films containing EA core–shell nanoparticles. The core–shell nanoparticles were synthesized through multistage seeded emulsion polymerization. The transmission electron microscopy (TEM) images revealed similar particle morphology and size in all EA nanoparticles. Differential scanning calorimetry (DSC) analysis confirmed the successful synthesis of core–shell particle morphology with two glass transition temperature (Tg) values (~12 °C and ~ 60 °C) observed for the core and shell layers, respectively. We observed an increase in the Tg values of the shell layer with higher EP content in the core layer. The use of EP-based copolymers raised the Tg values of the shell layer, significantly affecting the film formation behavior and their mechanical properties through interlayer crosslinking. Tensile modulus values for the films ranged from 200 to 500 MPa, marking the highest modulus reported for cast films of EA nanostructured films. Our findings reveal a straightforward and versatile method for producing high-modulus EA nanostructured films with customizable mechanical properties, making the model ideal for enhancing wood coating performance.

环氧丙烯酸酯(EA)核壳纳米粒子因其作为异质材料所具有的双重独特性能,尤其是在涂层应用方面的性能,近来受到了广泛关注。然而,芯层中环氧树脂(EP)浓度对机械性能的影响仍然有限,而且对其如何影响薄膜性能的机理也不甚了解。在本研究中,我们研究了芯层中环氧树脂浓度的变化对含有 EA 核壳纳米粒子的纳米结构薄膜力学性能的影响。核壳纳米粒子是通过多级种子乳液聚合法合成的。透射电子显微镜(TEM)图像显示,所有 EA 纳米粒子的形态和尺寸相似。差示扫描量热法(DSC)分析证实了核壳粒子形态的成功合成,并观察到核层和壳层分别具有两个玻璃化转变温度(Tg)值(~12 °C和~60 °C)。我们观察到,芯层中 EP 含量越高,外壳层的 Tg 值也越高。使用 EP 共聚物提高了外壳层的 Tg 值,通过层间交联显著影响了薄膜的形成行为及其机械性能。薄膜的拉伸模量值介于 200 到 500 兆帕之间,是目前所报道的 EA 纳米结构铸膜的最高模量。我们的研究结果揭示了一种生产具有可定制机械性能的高模量 EA 纳米结构薄膜的直接而通用的方法,使该模型成为提高木质涂层性能的理想选择。
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引用次数: 0
Pistachio shell-derived carbon dots and their screen-printing formulation for anticounterfeiting applications 开心果壳衍生碳点及其丝网印刷配方在防伪领域的应用
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-26 DOI: 10.1007/s11998-023-00894-0
H. D. Chinmayi, Namratha Ullal, Dhanya Sunil, Suresh D. Kulkarni, P. J. Anand, K. Udaya Bhat

In synergy with constructing a sustainable environment, facile reuse of carbon-rich biowastes as inexpensive precursors for the synthesis of value-added functional carbon dots (CDs) has garnered fruitful outcomes. Pistachio shells comprising cellulose, hemicellulose, and lignin were successfully utilized as a carbon source for the synthesis of CDs through carbonization and subsequent hydrothermal method. The methanolic fraction with desirable fluorescence in the visible region obtained after column purification of CDs was further characterized using TEM, EDS, SAED, FTIR, XPS, RS, XRD, and TCSPC techniques. The blue and green emitting CDs were used as colorants to prepare a water-based ink for screen printing. The screen prints on UV dull paper substrate exhibited good colorimetric and density values. The UV-induced yellow fluorescence of the ink film can be used as a security feature to authenticate genuine document/products and data storage.

Graphical abstract

在建设可持续发展环境的过程中,将富碳生物废料作为廉价前体用于合成高附加值的功能性碳点(CD)取得了丰硕成果。由纤维素、半纤维素和木质素组成的开心果壳被成功用作碳源,通过碳化和随后的水热法合成碳点。采用 TEM、EDS、SAED、FTIR、XPS、RS、XRD 和 TCSPC 等技术进一步表征了经柱纯化后获得的在可见光区域具有理想荧光的甲醇馏分。蓝色和绿色发光 CD 被用作着色剂来制备用于丝网印刷的水基油墨。在紫外线钝化纸基底上进行的丝网印刷显示出良好的色度和密度值。墨膜的紫外线诱导黄色荧光可用作防伪特征,以验证真实文件/产品和数据存储。
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引用次数: 0
Advances in emerging hydrogel fouling-release coatings for marine applications 海洋应用中新兴水凝胶污垢释放涂层的进展
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-23 DOI: 10.1007/s11998-023-00895-z
Michael Kio, Jeffery Klauda

The accumulation of microorganisms, algae, mussels, and barnacles on the hull of sea vessels leads to biofouling, surface corrosion, and increased drag as the vessel moves through water costing the marine industry around $15 billion/year. Current commercial traditional antifouling coatings suffer from reduced energy efficiency and short lifespan and contain heavy metals that are toxic to marine organisms and humans. The banning of these coatings is due to environmental concerns, and nonbiocidal alternatives such as polymer-based coatings are being sought after. This review demonstrates emerging promises of hydrogel fouling-release coatings (FRCs) in the marine environment that may be effective against a prevalent amount of biofouling agents. The review also highlights the importance of polymer backbone materials with surface wettability characteristics possessing hydrophobic, hydrophilic, and zwitterionic properties and further discusses emerging antifouling techniques, synthesis of hydrogel, swelling behavior of hydrogel, laboratory assays of hydrogel coating, marine field test, and outlook of hydrogel fouling-release (FRCs) coatings.

微生物、藻类、贻贝和藤壶在海船船体上的积累会导致生物污损、表面腐蚀以及船只在水中行驶时阻力增加,每年给海洋产业造成约 150 亿美元的损失。目前的商用传统防污涂料能效低、寿命短,而且含有对海洋生物和人类有毒的重金属。出于对环境的考虑,这些涂料已被禁用,人们正在寻求非杀菌的替代品,如聚合物基涂料。本综述展示了海洋环境中新出现的水凝胶污垢释放涂层(FRCs)的前景,这种涂层可有效抵御大量生物污损剂。综述还强调了具有疏水、亲水和齐聚物特性的表面润湿性聚合物骨架材料的重要性,并进一步讨论了新兴防污技术、水凝胶的合成、水凝胶的溶胀行为、水凝胶涂层的实验室检测、海洋现场测试以及水凝胶污垢释放涂层(FRCs)的前景。
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引用次数: 0
Preparation of active–passive anticorrosion antistatic epoxy nanocomposite coatings loaded with CeO2, CeO2@C, and CHS particles 制备负载有 CeO2、CeO2@C 和 CHS 颗粒的活性-被动防腐防静电环氧纳米复合涂层
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-22 DOI: 10.1007/s11998-023-00890-4
Sara Sabzavar, Mehdi Ghahari, Mehran Rostami, Morteza Ganjaee Sari

In this study, active–passive anticorrosion antistatic epoxy composite coatings containing CeO2, carbon coated ceria (CeO2@C), and carbon hollow sphere particles were prepared. Cerium oxide (CeO2) particles were synthesized through a hydrothermal approach in the presence of polyvinylpyrrolidone as a surfactant to achieve a uniform and semispherical morphology and to improve dispersion stability. Carbon hollow spheres (CHSs) were also fabricated using the surface-modified silica templating method. The structure and morphology of the synthesized particles were analyzed using Fourier transform infrared spectrometry, X-ray diffractometry, Raman spectrometry, and scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM-EDS). Furthermore, migration of the synthesized particles from the bulk toward the surface was investigated with atomic force microscopy, Raman spectra, and field emission SEM in addition to density, capillary wetting, contact angle, and zeta potential measurements. The results indicated that CHSs migrate toward the surface of the matrix due to its low interfacial tensions leading to a decline in the dielectric constant and electrical resistance, providing a composite with suitable antistatic properties. Moreover, electrochemical impedance spectroscopy and immersion testing were used to estimate the influence of the particles on the coating's anticorrosive property. The results showed that the impedance modulus at low frequency (|Z|0.01 Hz) significantly increased from 3.81 × 106 Ω cm2 (pristine epoxy) to 11 × 108 Ω cm2 after 40 days of immersion in 3.5% NaCl water solution. As a result of the synergistic protection provided by ceria, CHS, and CeO2@C particles, composite coatings exhibit superior anticorrosion properties. The ceria particles have an inhibitory effect which forms a passive layer. Furthermore, the CHS and CeO2@C particles produce a protective barrier prolonging the penetration pathway of corrosive media. Such significant improvements can provide an antistatic coating for designing novel corrosion protection coatings.

Graphical abstract

本研究制备了含有 CeO2、碳包覆铈(CeO2@C)和碳空心球颗粒的主动-被动防腐防静电环氧树脂复合涂层。氧化铈(CeO2)颗粒是在聚乙烯吡咯烷酮作为表面活性剂存在下通过水热法合成的,以获得均匀的半球形形态并提高分散稳定性。此外,还采用表面改性二氧化硅模板法制造了碳空心球(CHS)。利用傅立叶变换红外光谱法、X 射线衍射法、拉曼光谱法和扫描电子显微镜-能散射 X 射线光谱法(SEM-EDS)分析了合成颗粒的结构和形态。此外,除了密度、毛细管润湿性、接触角和 zeta 电位测量之外,还利用原子力显微镜、拉曼光谱和场发射扫描电镜研究了合成颗粒从体积向表面的迁移。结果表明,由于基质的界面张力较低,CHS 向基质表面迁移,导致介电常数和电阻下降,从而使复合材料具有合适的抗静电性能。此外,还利用电化学阻抗光谱和浸泡试验来评估颗粒对涂层防腐性能的影响。结果表明,在 3.5% NaCl 水溶液中浸泡 40 天后,低频(|Z|0.01 Hz)下的阻抗模量从 3.81 × 106 Ω cm2(原始环氧树脂)显著增加到 11 × 108 Ω cm2。由于铈、CHS 和 CeO2@C 颗粒的协同保护作用,复合涂层表现出卓越的防腐性能。铈颗粒具有抑制作用,可形成被动层。此外,CHS 和 CeO2@C 颗粒还能产生保护屏障,延长腐蚀性介质的渗透路径。这些重大改进可为设计新型防腐蚀涂层提供抗静电涂层。
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引用次数: 0
Dual-responsive wettability of poly o-toluidine nanofiber coating fabricated by interfacial polymerization 通过界面聚合制造的聚邻甲苯胺纳米纤维涂层的双响应润湿性
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-21 DOI: 10.1007/s11998-023-00889-x
Xianghui Xu, Hansong Zuo, Xiaoyan Zhou, Weiwei Wei, Yongqing Cao

To date, smart surfaces with controllable wettability have received extraordinary attention due to their great importance in both fundamental research and practical applications. Chemical composition and surface topography are the two key factors to affect the wettability of solid surfaces. Applying external stimuli to change the surface chemistry and/or topography is considered to be a valuable approach for driving the transition between hydrophilicity and hydrophobicity of surfaces. In this study, poly o-toluidine nanofibers were synthesized by a facile aqueous/organic interfacial polymerization, and superhydrophobic coatings of poly o-toluidine were prepared via a room-temperature spraying process. The reversible wettability conversion between the superhydrophobic and the hydrophilic state of the obtained poly o-toluidine coating under ultraviolet irradiation and electric stimulation was investigated. From the X-ray photoelectron spectroscopy analysis, this intelligent switching wetting behavior under ultraviolet light irradiation was confirmed to have a high correlation with the change in surface chemical composition. When the electric stimulation was applied, the wettability switch was caused by the redistribution of charge and electric dipole along the liquid–solid interface. 

迄今为止,具有可控润湿性的智能表面因其在基础研究和实际应用中的重要意义而受到了广泛关注。化学成分和表面形貌是影响固体表面润湿性的两个关键因素。施加外部刺激来改变表面化学成分和/或形貌被认为是推动表面亲水性和疏水性转变的重要方法。本研究采用水/有机界面聚合法合成了聚邻甲苯胺纳米纤维,并通过室温喷涂工艺制备了聚邻甲苯胺超疏水涂层。研究了所获得的聚邻甲苯胺涂层在紫外线照射和电刺激下在超疏水态和亲水态之间的可逆润湿转换。通过 X 射线光电子能谱分析,证实了紫外线照射下的这种智能切换润湿行为与表面化学成分的变化高度相关。当施加电刺激时,润湿性切换是由电荷和电偶极子沿液固界面的重新分布引起的。
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引用次数: 0
Simulation analysis of the start-up process of Carreau-type fluid slot die coating Carreau 型流体槽模具涂层启动过程的模拟分析
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-15 DOI: 10.1007/s11998-023-00891-3
Shaofei Pan, Yikun Wei, Jianneng Chen, Chuanyu Wu, Jiangming Jia

The start-up process is important for ensuring the end quality of slot coating products. This study uses ANSYS Fluent to explore the start-up process of slot coating with Carreau-type non-Newtonian fluid. The relationship between the pressure change in the coating bead at the slot outlet and the stabilization process of the coating bead is analyzed, and the effects of the downstream die lip angle and downstream die lip length on the size of the coating bead are discussed. The simulation results show that the pressure at the slot outlet directly affects the stabilization of the coating bead, and accelerating the coating bead stabilization pressure can accelerate the start-up process. When other parameters remain unchanged, reducing the downstream die lip angle or length can reduce the size of the coating bead, thereby accelerating the start-up process.

启动过程对于确保槽涂层产品的最终质量非常重要。本研究使用 ANSYS Fluent 探索了使用 Carreau 型非牛顿流体的槽涂层的启动过程。分析了槽出口处涂覆珠压力变化与涂覆珠稳定过程之间的关系,讨论了下游模唇角度和下游模唇长度对涂覆珠尺寸的影响。模拟结果表明,槽出口处的压力直接影响涂膜珠的稳定,加快涂膜珠稳定压力可加快启动过程。在其他参数不变的情况下,减小下游模唇角度或长度可以减小涂膜珠的尺寸,从而加快启动过程。
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引用次数: 0
Biodegradable surfactants do not improve antifouling or fouling-release performance of polydimethylsiloxane 生物降解表面活性剂无法改善聚二甲基硅氧烷的防污或污垢释放性能
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-13 DOI: 10.1007/s11998-023-00884-2
Emmerson R. Wilson, Katerina Basque, Meaghan MacDonald, Amelia F. MacKenzie, Michelle Hodgson, Robin Stuart, Truis Smith-Palmer, Russell C. Wyeth

Surfaces that combine low-toxicity antifouling effects with fouling-release properties are an intriguing possibility for developing effective measures against marine biofouling. This study field tested siloxane-based fouling-release surfaces enhanced by adding biodegradable surfactants. Two different surfactants were added to a standard polydimethylsiloxane (PDMS) surface, as well as to PDMS soaked in silicone oil, and compared to controls without surfactant augmentation. Antifouling and fouling-release performance was assessed over 11 to 13 weeks against the most prominent fouling species at three locations in Cape Breton, Nova Scotia, Canada. Using nonlinear mixed effect analysis, surfactants were found to have little impact on the progression of biofouling on PDMS without silicone oil in all three sites and had no additional impact on the progression of biofouling on PDMS augmented with silicone oil. (Silicone oil was found to delay biofouling in PDMS without other additives.) Given the known toxicity of some surfactants to invertebrate larvae, future efforts should consider either higher concentrations or alternative varieties for incorporation into fouling-release surfaces.

兼具低毒性防污效果和污垢释放特性的表面是开发有效的海洋生物污垢防治措施的一种令人感兴趣的可能性。本研究实地测试了通过添加可生物降解的表面活性剂而增强的硅氧烷基污垢释放表面。在标准聚二甲基硅氧烷(PDMS)表面和浸泡在硅油中的聚二甲基硅氧烷表面添加了两种不同的表面活性剂,并与未添加表面活性剂的对照组进行了比较。在加拿大新斯科舍省布雷顿角的三个地点,针对最主要的污垢种类进行了为期 11 至 13 周的防污和污垢释放性能评估。通过非线性混合效应分析,发现表面活性剂对所有三个地点不含硅油的 PDMS 上生物污垢的发展影响甚微,对添加了硅油的 PDMS 上生物污垢的发展也没有额外的影响(发现硅油在不添加其他添加剂的情况下也能延缓 PDMS 上生物污垢的发展)。 考虑到某些表面活性剂对无脊椎动物幼虫的已知毒性,未来的研究应考虑在污垢释放表面添加更高浓度的表面活性剂或替代品。
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引用次数: 0
Antimicrobial surface coating as a pathway to curb resistance: preparation, mode of action and future perspective 作为抑制抗药性途径的抗菌表面涂层:准备工作、作用模式和未来展望
IF 2.3 4区 材料科学 Q2 CHEMISTRY, APPLIED Pub Date : 2024-02-12 DOI: 10.1007/s11998-023-00879-z
Vincent Ngunjiri Mwangi, Edwin Shigwenya Madivoli, Mourine Kangogo, Sammy Indire Wanakai, Walyambillah Waudo, Dennis Mwanza Nzilu

Antimicrobial resistance has proven to be an existential threat that endangers the health of human beings. The ease of accessing conventional antibiotics, and their unlimited and unregulated use and often misuse is seen to be a contributing factor to the rise in the resistance of microbes toward medications. The overuse of these medications in the agricultural sector also adds to the rising burden of antibiotic resistance. In line with efforts to counter the threat of antimicrobial resistance and the menace of hospital acquired infections developing antimicrobial surface coatings that can eliminate microbes that get deposited on those coatings is essential. This review aims to bring an understanding of antimicrobial resistance mechanisms, the preparation and mode of action and the future perspective of the antimicrobial surface coatings.

摘要 抗菌药耐药性已被证明是一种危及人类健康的生存威胁。传统抗生素的易得性、无限制和无管制的使用,以及经常出现的滥用,被认为是导致微生物耐药性上升的一个因素。农业部门过度使用这些药物也加重了抗生素耐药性的负担。为了应对抗菌药耐药性的威胁和医院感染的威胁,必须开发能够消灭沉积在抗菌表面涂层上的微生物的抗菌表面涂层。本综述旨在介绍抗菌剂的抗药性机制、制备方法和作用模式以及抗菌表面涂层的未来前景。
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引用次数: 0
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Journal of Coatings Technology and Research
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