Development of electroless silver plating on Para‐aramid fibers and growth morphology of silver deposits

The development of a conductive fiber with flame resistance is an urgent concern particularly in national defense and other specialized fields. Aramid fibers (para‐ or meta‐) exihibit high strength and excellent fire resistance. Electroless silver plating on para‐aramid fibers and growth morphology of silver deposits was investigated in the present work. The surface of para‐aramid fibers was roughened using sodium hydride/dimethyl sulfoxide to guarantee successful electroless plating. Two complexing agents (ethylene diamine/ammonia) and two reducing agents (glucose/seignette salt) were used for the electroless silver plating bath design. Structure and properties of the resulting silver‐deposited para‐aramid fibers were evaluated based on scanning electron microscopy, silver weight gain percentage calculation, electrical resistance measurement, crystal structure analysis, and mechanical properties test. The results showed that a higher silver weight gain was advantageous to the improvement of conductivity for the silver‐deposited para‐aramid fibers. The obtained silver deposit was homogenous and compact. Electroless silver‐plating deposits were considered to be three‐dimensional nucleation and growth model (Volmer–Weber). Black, silver gray, and white deposits appeared sequentially with progressive plating. The breaking strength of silver‐deposited para‐aramid fibers remained at value up to 44 N. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Characterization of Cu Nanoparticles on TiO2 Photocatalysts Fabricated by Electroless Plating Method

Cu-modified TiO₂ photocatalysts (Cu/TiO₂) were fabricated by electroless plating and wet impregnation methods. Photocatalytic activity for H₂ production over Cu/TiO₂ by electroless plating method was higher than that over Cu/TiO₂ by impregnation method. Characterization of Cu nanoparticles by HRTEM, STEM-EDX, XRD and XAFS was studied. As compared to the wet impregnation method, the electroless plating method resulted in the formation of Cu nanoparticles with small size and uniform distribution on the TiO₂ surface, which caused the enhancement of H₂ production. XAFS measurement provided the evidences for the chemical state change of Cu species during the photocatalytic reaction. The process that Cu species varied from Cu²⁺ into Cu⁰ via Cu¹⁺ as the intermediate under photoirradiation is very important for the H₂ production, which indicates that the metallic Cu nanoparticles acted as the active sites and restrained the photogenerated charges recombination.     

A new electroless Ni plating procedure of iodine-treated aramid fiber

A new, durable, etchant- and tin-free catalyzation process was studied for electroless nickel metallization of aramid fiber via iodine pretreatment. Firstly, iodine components were selectively doped onto the inner part of the fiber using vapor iodine exposure followed by treatment with a tin-free acidic palladium chloride solution to form palladium iodide (PdI₂) on the fiber surface. After subsequent reduction of PdI₂ into metal palladium (Pd), electroless plating was carried out. A uniform Ni plating layer was formed on the fiber surface, which exhibited high durability against resistance tests of ultrasonic exposure, tape peel-off, and corrosion in NaCl solution. Here, Pd particles that formed at the inner part near the fiber surface functioned as an anchor of the plated layer as well as a catalyst of electroless plating. Investigation of the plate bath composition shows that the use of anionic surfactant enhances the adhesion of the plated layer with fiber matrix, while a reducing agent in the plate bath reduces the smoothness of the plated surface. Also, the plate bath pH and the temperature of the plating solution control the layer deposition rate noticeably more than does the plating time. The proposed method retained good tensile strength in the plated fiber. Ni-plated aramid fiber exhibited durable electrical conductivity and magnetic properties.     

Experimental and theoretical studies on the adjustable thermal properties of epoxy composites with silver‐plated short fiberglass

This article investigates the evolution of the thermal conductivity and the coefficient of thermal expansion (CTE) of epoxy composites filled with different silver‐plated short glass fibers (Ag@GFs) treated by electroless plating. After electroless plating, the results of X‐ray diffraction and scanning electron microscopy showed that glass fibers were coated with pure silver shells whose thickness was controlled via the repetition of electroless plating cycle, and calculated by weighting method. The optical photographs showed that Ag@GFs are randomly oriented and uniformly dispersed in the composites. HotDisk thermal constant analyzer and dilatometer were used to further characterize the thermal conductivity and the CTE of the composites, respectively. The results revealed that the thermal conductivity of Ag@GF/epoxy composites increased with the increase of Ag@GF content, and was adjusted by changing the thickness of silver shell. But the CTE of the composites drops sharply as the Ag@GF content increases compared with neat epoxy. Based on Agari model with fitted factors of C_p and C_f, the calculated thermal conductivity values of Ag@GF/epoxy composites agreed well with the experimental results, and C_p kept almost unchanged, but C_f varied with the change of the thickness of silver shell, despite increasing filler content. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45555.     

Electromagnetic shielding and corrosion resistance of electroless Ni‐P and Ni‐P‐Cu coatings on polymer/carbon fiber composites

In order to study electrical properties, especially the electromagnetic interference (EMI) shielding property of ternary Ni‐P‐Cu plated polyether ether ketone/carbon fiber composites (CFs/PEEK) and their dependence on Cu content of the coating, electroless Ni‐P coating was first deposited on CFs/PEEK to obtain the optimum conditions for deposition rate, then a small quantity of CuSO₄•5H₂O (0.1∼0.4 g/L) was added in the electroless nickel‐based alloy plating (ENP) bath to investigate the influence of Cu content on the deposition rate and coating characterizations. The EMI shielding effectiveness (SE) was evaluated and corrosion resistance was characterized by electrochemical polarization measurement. It was found that coating phase change from amorphous to a mixture of amorphous and microcrystalline phases with the increase of Cu²⁺ concentration. Due to the neat morphology and uniform amorphous structure, the optimum coating Ni‐P‐2.2 wt% Cu obtained at the 0.2 g/L Cu²⁺ in the bath owns the best corrosion resistance, EMI SE and the lowest surface resistance. POLYM. COMPOS., 36:923–930, 2015. © 2014 Society of Plastics Engineers     

碳纤维布化学镀铜工艺的研究

采用以甲醛为还原剂的化学镀铜液,用硝酸银作活化剂,在碳纤维布表面沉积出连续、均匀、有光泽的化学镀铜层。研究了不同前处理工艺对碳纤维布化学镀铜的影响。采用扫描电子显微镜表征了化学镀铜层的表面形貌,并用数字电压表测试了碳纤维布化学镀铜前后的导电性。     

Electroless copper plating using Fe as a reducing agent

Although the electroless plating method is known to be an effective method for obtaining fine wiring in particular, 1 mol hydrogen gas is generated during 1 mol Cu deposition, and voids are generated in the wiring when electroless Cu plating is applied to fine wiring. To avoid the hydrogen evolution, the possibility of performing electroless Cu plating was confirmed using an inexpensive Fe^II compound as a reducing agent. The bath contains CuSO₄, FeSO₄, NaCl, ethylenediamine, sodium citrate, polyethylene glycol (PEG), and 2,2′-bipyridine. Under optimal conditions, over 1.7 μm of copper deposit with a smooth surface was obtained after 3 h of plating, which did not contain iron as an impurity. The electrical resistivity of the copper film is about 3-4 μΩ cm corresponding to that of electroplated copper films.     

Formation of bead‐free and core–shell superfine electrospinning fibers under the assistance of another polymer and an interfacial compatibilizer

This work presents a new way of preparing bead‐free and core–shell superfine polymer electrospinning fibers under the assistance of another polymer and an interfacial compatibilizer. For the electrospinning of polystyrene (PS)/CHCl₃ solution, the bead‐free fiber cannot be obtained until the PS concentration is above 0.25 g/mL but its average diameter is above 10 μm. Using polyamide 6 (PA6) as an additive, the critical concentration capable of forming bead‐free fiber greatly decreased and core–shell fibers with PA6 as the core and PS as the shell were obtained due to the driving effect of high spinability of PA6. The introduction of a copolymer (PS‐co‐TMI) of styrene (St) and 3‐isopropenyl‐α,α‐dimethylbenzene isocyanate (TMI) can react with amine of PA6 to form the copolymer of PS and PA6 as an interfacial compatibilizer. As a result, it can further enhance the dispersion and deformation of minor component PA6 into uniform microfiber core, and drive PS to uniformly cover the surface of PA6 fibers, and finally form bead‐free and core–shell superfine fibers. POLYM. ENG. SCI., 59:1437–1444 2019. © 2019 Society of Plastics Engineers     

Surface modification of nylon‐6 fibers for medical applications

Hydroxyethylmethacrylate (HEMA) is considered to be one of the important vinyl monomers. The ability of polyhydroxyethyl‐methacylate (PHEMA) graft sites to consecutive chemical modification makes the use of nylon‐6 fibers grafted with PHEMA a feasible bed for immobilization of a wide range of biologically active reagents, specially enzymes, drugs, cells, and immunadsorbents. Stemming from the above discussions, in this article, the graft copolymerization of HEMA onto modified nylon‐6 fibers containing Polydiallyldimethylammonium chloride (PDADMAC) in the presence of Cu²⁺–K₂S₂O₈ as a redox initiating system was carried out, with very high rate and almost without homopolymer formation. The factors affecting the grafting reaction (monomer, K₂S₂O₈ and cupric ion concentrations, the amount of PDADMAC as well as the reaction temperature) were studied. Kinetic investigation revealed that the rate of grafting (R_p) of HEMA onto modified nylon‐6 fibers is proportional to [HEMA]¹, [CuSO₄.5H₂O] ^0.7, [PDADMAC]^0.4, and [K₂S₂O₈]^1.4. The overall activation energy was calculated (71 KJ/mol). The fine structure, surface topography, thermal and electrical properties of parent and grafted nylon‐6 fibers were investigated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3788–3796, 2007     

石英光纤表面化学镀镍磷合金工艺

引　言石英光纤广泛应用于光通信、光传感等领域 ,利用它制作的光纤传感器可用来测量物体的应力和应变 .但在测量前应先将传感器牢固地固定在待测物体上 ,常用的固定方法是使用环氧树脂等胶黏剂 ,这种方法存在着致命的缺点 ,即胶黏剂与待测物体和光纤涂覆层之间、光纤芯层和光纤涂覆层之间会产生相对移动 ,使得测量的数据不能真实地反映待测物体的应力和应变[1,2 ] .因此 ,若能将石英光纤表面金属化 ,然后用锡焊的方法使光纤固定在　　Receiveddate:2 0　待测物体上 ,这一难题将会完全解决 .光纤表面金属化有多种方法可以实现 ,常用的方法…     

Antimicrobial activity of bleached cattail fibers (Typha domingensis) impregnated with silver nanoparticles and benzalkonium chloride

Typha domingensis (Cattail) fiber is a significant natural resource, abundant in cellulose. The study reports the useful utilization of T. domingensis fiber for physicochemical impregnation of silver nanoparticles and benzalkonium chloride, in the development of a material with antimicrobial activity. The fibers were pre-treated with alkaline hydrogen peroxide (bleaching) for partial removal of lignin, pectin and waxes. Subsequently treated in a solution of different concentrations of benzalkonium chloride and Tollens' reagent. The new materials obtained were carefully investigated for their structure and thermal stability, morphology and susceptibility to antimicrobials (Staphylococcus aureus, Escherichia coli, Salmonella typhimuruim, and Salmonella enteritidis). Fourier transform infrared spectra showed the presence of benzalkonium chloride. The morphology analysis showed the silver nanoparticles on the surface of the bleached fibers. The susceptibility profile to antimicrobials was confirmed by the formation of inhibition halos (≅11.26 mm). Based on the properties of the materials obtained, it can be concluded that the modified cattail fibers have the potential to be used as a functional filler, or coating, in the development of antimicrobial composites.     

Incorporation of reactive silver‐tricalcium phosphate nanoparticles into polyamide 6 allows preparation of self‐disinfecting fibers

Polymer fibers are used for a wide range of materials in contact with the human body. Since bacterial contamination may cause diseases, it is desirable to provide fibers with antimicrobial properties. This work investigates the ability of silver‐tricalcium phosphate nanoparticles (Ag/TCP) to build a reactive system when incorporated in polyamide fibers. In the presence of bacteria, the TCP carrier particles are biodegraded and trigger the release of silver. For this work, Ag/TCP nanoparticles (1.3 wt% silver) were produced by flame spray synthesis and subsequently processed with polyamide 6 to fibers (125‐μm thick, containing 260 ppm silver) with the aid of extrusion and melt‐spinning for subsequent antibacterial testing. The fibers were contaminated with the clinically relevant strains Escherichia coli or Streptococcus sanguinis, respectively. The reactive fibers demonstrated significantly reduced plate count within 24 h (the number of colony forming units was reduced by 99.999% with E. coli and 99.6% with S. sanguinis compared with pure PA6 reference fibers). These reactive properties of easily integrated antibacterial silver suggest an implementation of intelligent fibers to a wide range of applications. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Enhanced photocatalytic properties of a novel GO-Ag-C6H5Ag3O7 nanocomposite

A novel graphene oxide-Ag-C₆H₅Ag₃O₇ nanocomposite was prepared by a facile precipitation reaction with the aid of photo-reduction. The rich surface functional groups of graphene oxide (GO) interacted with silver cations, provided the nucleation sites and induced the formation of C₆H₅Ag₃O₇ nanoparticles on the GO surface uniformly. The nanocomposite displayed an enhanced photocatalytic activity compared with pure C₆H₅Ag₃O₇ and GO under simulated sunlight, due to the reduced recombination of plasmon-induced electron–hole pairs on the Ag nanoparticles by the GO. This study likely provides one possibility of exploiting stable Ag/silver (I) complex photocatalysts in dealing with environmental contaminants.     

Electrospun soy‐protein‐based nanofibrous membranes for effective antimicrobial air filtration

Soy proteins are gaining more and more attention because of its multifunction and biodegradability. Silver nanoparticles (AgNPs) are introduced into the nanofibers to prevent growth of microorganisms over the filter media. In the present study, the multifunctional and antimicrobial nanofibrous membranes were prepared by electrospinning the soy protein isolate (SPI)/polymide‐6 (PA6)‐silver nitrate system followed by ultraviolet reduction. The morphology of SPI/PA6 nanofibrous membranes was characterized by scanning electron microscopy. Antibacterial property of nanofibrous membranes were investigated against Escherichia coli and Bacillus subtilis. The optimized fiber membrane exhibited over 95% filtration efficiency of PM_0.3 (particulate matter size less than 0.3 μm). The successful synthesis of SPI/PA6‐AgNPs nanofibrous membranes would make it to be the potential candidate for novel antibacterial and high‐performance air filter. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45766.     

Study on depositing SiO2 nanoparticles on the surface of jute fiber via hydrothermal method and its reinforced polypropylene composites

To improve the interfacial compatibility of jute fiber reinforced polypropylene (PP) composites, hydrothermal method was used to deposit SiO₂ nanoparticles on the surface of pretreated jute fibers and the effect of reaction factors (tetraethoxysilane [TEOS] concentration, ammonia concentration, and reaction temperature) on the deposition of SiO₂ nanoparticles were evaluated. The results of FTIR, XRD, SEM, and TEM showed that the amorphous SiO₂ nanoparticles with an average particle size of 65.0 nm were successfully deposited on the surface of jute fibers at the TEOS/H₂O volume ratio of 1:2, ammonia of 0.55 M, reaction temperature of 100 °C (0.15 MPa) for 5 h. Compared with the sol–gel method, SiO₂ nanoparticles obtained by the hydrothermal method possessed smaller particle size and were less agglomerated, which can better fill in the surface defects of the jute fibers and result in a 12.9% increase in the tensile strength. The study on the mechanical properties and interface performance of the jute fiber reinforced PP composites indicated that the interfacial compatibility between jute fibers and PP was obviously improved. The tensile and impact strength of the composites reinforced with nano‐SiO₂ deposited jute fibers were increased by 26.87% and 25.65%, respectively, compared with the untreated jute fibers. J. VINYL ADDIT. TECHNOL., 26:43–54, 2020. © 2019 Society of Plastics Engineers     

Comparative Study of Silver Nanoparticles Coated and Uncoated NiO–Fe2O3–CaO–SiO2–P2O5 Ferromagnetic Bioactive Ceramics

Bioactive ferromagnetic ceramics of system xNiO–(3?x)Fe₂O₃–52CaO–30SiO₂–15P₂O₅, (x = 0, 3 mol%) have been prepared in the laboratory using sol–gel technique. Silver nanoparticles coating has been undertaken on the surface of synthesized samples. Comparative study of silver nanoparticles coated and uncoated samples has been undertaken with the help of transmission electron microscopy, X‐ray diffraction (XRD), degradation, drug delivery, hemolysis, antimicrobial, and cell culture studies. XRD patterns indicate the growth of hydroxyl apatite layer on the surface of coated as well as uncoated samples. Ferromagnetic properties of samples have been investigated with the help of vibrating sample magnetometer technique. Samples have shown good response as drug carriers under normal conditions as well as under the influence of magnetic field. Drug release mechanism and mesoporus nature of samples have been investigated with the help of Brunauer–Emmett–Teller technique. Nonreactivity of samples (coated and uncoated) with red blood cells and white blood cells show nontoxic nature of the samples. Coated samples have shown better antimicrobial properties against six different microorganisms, including some resistive strain like methicillin‐resistant Staphylococcus aureus with minimum inhibitory concentration of 0.05 mg/ml as compared to uncoated samples. It has been observed that samples also provide a healthy environment for the growth of MG 63 cell lines. It has been noticed that presence of silver nanoparticles on the surface of samples improve degradation and antimicrobial properties.     

The issue of selectivity in the direct synthesis of H2O2 from H2 and O2: the role of the catalyst in relation to the kinetics of reaction

The kinetic behavior in the direct synthesis of H₂O₂ with Pd–Me (Me = Ag, Pt) catalysts prepared by depositing the noble metals by electroless plating deposition (EPD) or deposition–precipitation (DP) methods on α-Al₂O₃ asymmetric ceramic membrane with or without a further surface coating by a carbon thin layer is reported. The effect of the second metal with respect to Pd-only catalysts considerably depends on the presence of the carbon layer on the membrane support. Several factors in the preparation of these membranes as well as the reaction conditions (temperature, concentration of Br⁻, pH) determine the selectivity in H₂O₂ formation, influencing the rate of the consecutive reduction of H₂O₂ (which is faster with respect to H₂O₂ decomposition on the metal surface) and/or of direct H₂ + O₂ conversion to H₂O. Defective Pd sites are indicated to be responsible for the two unselective reactions leading to water formation (parallel and consecutive to H₂O₂ formation), but the rate constants of the two reactions are differently influenced from the catalytic membrane characteristics. Increasing the noble metal loading on the membrane not only increases the productivity to H₂O₂, but also the selectivity, due to the formation of larger, less defective, Pd particles.     

Characterization of polyaniline/Ag nanocomposites using H2O2 and ultrasound radiation for enhancing rate

Polyaniline/Ag nanocomposites have been synthesized via in situ chemical oxidation polymerization of aniline in silver salt by sonochemical method using H₂O₂ as an external medium. H₂O₂ was used to reduce AgNO₃ to Ag nanoparticles as well as to polymerize aniline to polyaniline in the same pot. The ultrasound radiation as an energy source was applied to facilitate the reaction by reducing the reaction time. Reduction of the silver salt in aqueous aniline leads to the formation of silver nanoparticles which in turn catalyze oxidation of aniline to polyaniline. The research on the structures and properties of the composites showed the individual or aggregated silver nanoparticles are dispersed in the matrix of polyaniline. The composites possess a higher degradation temperature than polyaniline alone, and their electrical conductivity are raised morethan 200 times. The cyclic voltammetry and impedance spectroscopy results showed that the polyaniline/Ag film exhibits considerably higher electroactivity compared with polyaniline film without Ag particles. POLYM. COMPOS., 31:1662–1668, 2010. © 2009 Society of Plastics Engineers     

Preparation and antibacterial activity of polyvinyl alcohol/regenerated silk fibroin composite fibers containing Ag nanoparticles

Polyvinyl alcohol (PVA)/regenerated silk fibroin (SF)/AgNO₃ composite nanofibers were prepared by electrospinning. A large number of nanoparticles containing silver were generated in situ and well‐dispersed nanoparticles were confirmed by transmission electron microscopy (TEM) intuitionally. Ultraviolet (UV)‐visible spectroscopy and X‐ray diffraction (XRD) patterns indicated that nanoparticles containing Ag were present both in blend solution and in composite nanofibers after heat treatment and after subsequent UV irradiation. By annealing the nanofibers, Ag⁺ therein was reduced so as to produce nanoparticles containing silver. By combining heat treatment with UV irradiation, Ag⁺ was transformed into Ag clusters and further oxidized into Ag₃O₄ and Ag₂O₂. Especially size of the nanoparticles increased with heat treatment and subsequent UV irradiation. This indicated that the nanoparticles containing silver could be regulated by heat treatment and UV irradiation. The antimicrobial activity of heat‐treated composite nanofibers was evaluated by Halo test method and the resultant nanofibers showed very strong antimicrobial activity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The effects of surface treatments of fibers on the interfacial properties in single-fiber composites

The interfacial properties between fibers and the matrix contribute to the overall properties in high performance composites. Plasma treatments (Ar, O₂, CF₄/O₂, N₂/H₂) have been performed on carbon fibers to improve the fiber-matrix interaction. The treatment efficiency was checked by the single-fiber technique, while the surface chemistry and morphology were characterized by X-ray photoelectron spectroscopy (XPS), static secondary ion mass spectroscopy (SSIMS), and scanning electron microscopy (SEM). The O₂- and N₂/H₂-plasma treatments proved most effective both for introducing oxygen-containing functionalities at the fiber surface and for improving the interfacial shear strength of carbon fiber/epoxy composites. A relationship between the oxygen concentration at the fiber surface and the interfacial shear strength is demonstrated.