Cellulose acetate hollow fiber membrane from banana stem fibers coated by TiO2 (CAHFMT) was prepared and characterized as an alternative material for degradation of waste textile dye. Its applicability was demonstrated by mechanical properties, FTIR, SEM, thermal resistance, performance, and degradation efficiency. Cellulose acetate (CA) was synthesized from banana stem fibers by swelling stage, acetylation reaction, and hydrolysis reaction. CA was modified using TiO2 of various concentrations. CAHFMT with 22 % w/v dope concentration has the optimum mechanical properties (stress, strain and Young’s modulus), as well as hydrophilic properties. The performances of CAHFMT with Congo red were determined. The SEM results showed that the membrane had rigid pores. Moreover, this research stated that CAHFMT could be a solution to overcome economical and effective problems.
{"title":"Cellulose Acetate Hollow Fiber Membranes from Banana Stem Fibers Coated by TiO2 for Degradation of Waste Textile Dye","authors":"S. Wafiroh, A. Abdulloh, A. A. Widati","doi":"10.23939/CHCHT15.02.291","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.291","url":null,"abstract":"Cellulose acetate hollow fiber membrane from banana stem fibers coated by TiO2 (CAHFMT) was prepared and characterized as an alternative material for degradation of waste textile dye. Its applicability was demonstrated by mechanical properties, FTIR, SEM, thermal resistance, performance, and degradation efficiency. Cellulose acetate (CA) was synthesized from banana stem fibers by swelling stage, acetylation reaction, and hydrolysis reaction. CA was modified using TiO2 of various concentrations. CAHFMT with 22 % w/v dope concentration has the optimum mechanical properties (stress, strain and Young’s modulus), as well as hydrophilic properties. The performances of CAHFMT with Congo red were determined. The SEM results showed that the membrane had rigid pores. Moreover, this research stated that CAHFMT could be a solution to overcome economical and effective problems.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74248000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
B. Korchak, O. Grynyshyn, T. Chervinskyy, A. Nagurskyy, V. Stadnik
The scheme of the integrated regeneration method for used mineral motor oils (UMMO) has been developed, according to which M-10DM and NORMAL 15W40 used oils were regenerated. A study on changes in physico-chemical properties, qualitative and elemental composition was carried out, and a mathematical model of the process was built. The further applications of the obtained products were proposed. Based on the obtained results, the technological scheme and flow chart of UMMO integrated regeneration were developed, and the process material balance was calculated.
{"title":"Integrated Regeneration Method for Used Mineral Motor Oils","authors":"B. Korchak, O. Grynyshyn, T. Chervinskyy, A. Nagurskyy, V. Stadnik","doi":"10.23939/CHCHT15.02.239","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.239","url":null,"abstract":"The scheme of the integrated regeneration method for used mineral motor oils (UMMO) has been developed, according to which M-10DM and NORMAL 15W40 used oils were regenerated. A study on changes in physico-chemical properties, qualitative and elemental composition was carried out, and a mathematical model of the process was built. The further applications of the obtained products were proposed. Based on the obtained results, the technological scheme and flow chart of UMMO integrated regeneration were developed, and the process material balance was calculated.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91244307","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
P. N. S. Pathirannehe, T. D. Fernando, C. Rajapakse
In this study, physically and chemically modified chitosan; protonated glycerol diglycidyl ether cross-linked chitosan beads (GDCLCB/H+) were prepared and characterized using FTIR and SEM. The optimum defluoridation capacity (DC) of GDCLCB/H+ was observed at the initial F- ion concentration of 15 mg/l, adsorbent dosage of 0.6 g, contact time of 30 min and pH of the solution was in the range of 5–7 at 303 ± 2 K. The equilibrium adsorption data fitted well with Langmuir and Freundlich isotherm models. The maximum adsorption capacity (q0), obtained from Langmuir isotherm for F-adsorption was found to be 2000 mg/kg, which was significantly higher than that of unmodified chitosan (192.3 mg/kg) and most of the chitosan-based sorbents reported in the literature. Water samples collected from Medawachchiya, Sri Lanka, were treated with the adsorbents and the results suggested that GDCLCB/H+ could be used as an effective defluoridation agent.
{"title":"Removal of Fluoride from Drinking Water Using Protonated Glycerol Diglycidyl Ether Cross-Linked Chitosan Beads","authors":"P. N. S. Pathirannehe, T. D. Fernando, C. Rajapakse","doi":"10.23939/CHCHT15.02.205","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.205","url":null,"abstract":"In this study, physically and chemically modified chitosan; protonated glycerol diglycidyl ether cross-linked chitosan beads (GDCLCB/H+) were prepared and characterized using FTIR and SEM. The optimum defluoridation capacity (DC) of GDCLCB/H+ was observed at the initial F- ion concentration of 15 mg/l, adsorbent dosage of 0.6 g, contact time of 30 min and pH of the solution was in the range of 5–7 at 303 ± 2 K. The equilibrium adsorption data fitted well with Langmuir and Freundlich isotherm models. The maximum adsorption capacity (q0), obtained from Langmuir isotherm for F-adsorption was found to be 2000 mg/kg, which was significantly higher than that of unmodified chitosan (192.3 mg/kg) and most of the chitosan-based sorbents reported in the literature. Water samples collected from Medawachchiya, Sri Lanka, were treated with the adsorbents and the results suggested that GDCLCB/H+ could be used as an effective defluoridation agent.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78955696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
O. Vakhula, M. Pona, Solokha Ivan, O. Koziy, M. Petruk
The issue of cordierite-mullite refractories protection from the influence of aggressive factors is considered. The interaction between the components of protective coatings has been studied. It has been investigated that in the systems based on poly(methylphenylsiloxane) filled with magnesium oxide, alumina and quartz sand, the synthesis of cordierite (2MgO•2Al2O3•5SiO2), mullite (3Al2O3•2SiO2) or magnesium aluminate spinel (MgO•Al2O3) is possible. The basic composition of the protective coating, which can be recommended for the protection of cordierite-mullite refractory, is proposed.
{"title":"Ceramic Protective Coatings for Cordierite-Mullite Refractory Materials","authors":"O. Vakhula, M. Pona, Solokha Ivan, O. Koziy, M. Petruk","doi":"10.23939/CHCHT15.02.247","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.247","url":null,"abstract":"The issue of cordierite-mullite refractories protection from the influence of aggressive factors is considered. The interaction between the components of protective coatings has been studied. It has been investigated that in the systems based on poly(methylphenylsiloxane) filled with magnesium oxide, alumina and quartz sand, the synthesis of cordierite (2MgO•2Al2O3•5SiO2), mullite (3Al2O3•2SiO2) or magnesium aluminate spinel (MgO•Al2O3) is possible. The basic composition of the protective coating, which can be recommended for the protection of cordierite-mullite refractory, is proposed.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79306112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
O. Mukbaniani, J. Aneli, T. Tatrishvili, E. Markarashvili
Hydrosilylation reactions of 2,4,6,8-tetrahydro-2,4,6,8-tetramethylcyclotetrasiloxane (D4H) with 2,2,3,3,4,4,5,5-octafluoropentyl acrylate at 1:4.2 ratio of initial compounds catalysed by platinum catalysts have been studied and corresponding adduct D4R' has been obtained. Ring opening polymerization of D4R in the presence of dry potassium hydroxide has been carried out and comb-type polymers with 2,2,3,3,4,4,5,5-octafluoropentyl propionate side groups have been obtained. The synthesized product D4R and polymers were analyzed by FTIR, 1H, 13C, and 29Si NMR spectroscopy. The solid polymer electrolyte membranes have been obtained via sol-gel reactions of polymers with tetraethoxysilane doped with lithium trifluoromethylsulfonate (triflat) and lithium bis(trifluorosulfonyl)imide. It has been found that the electric conductivity of the polymer electrolyte membranes at room temperature changes in the range of (1.9•10-6) – (5.9•10-10) S•cm-1.
{"title":"Solid Polymer Electrolyte Membranes on the Basis of Fluorosiloxane Matrix","authors":"O. Mukbaniani, J. Aneli, T. Tatrishvili, E. Markarashvili","doi":"10.23939/CHCHT15.02.198","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.198","url":null,"abstract":"Hydrosilylation reactions of 2,4,6,8-tetrahydro-2,4,6,8-tetramethylcyclotetrasiloxane (D4H) with 2,2,3,3,4,4,5,5-octafluoropentyl acrylate at 1:4.2 ratio of initial compounds catalysed by platinum catalysts have been studied and corresponding adduct D4R' has been obtained. Ring opening polymerization of D4R in the presence of dry potassium hydroxide has been carried out and comb-type polymers with 2,2,3,3,4,4,5,5-octafluoropentyl propionate side groups have been obtained. The synthesized product D4R and polymers were analyzed by FTIR, 1H, 13C, and 29Si NMR spectroscopy. The solid polymer electrolyte membranes have been obtained via sol-gel reactions of polymers with tetraethoxysilane doped with lithium trifluoromethylsulfonate (triflat) and lithium bis(trifluorosulfonyl)imide. It has been found that the electric conductivity of the polymer electrolyte membranes at room temperature changes in the range of (1.9•10-6) – (5.9•10-10) S•cm-1.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77291528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Bratychak, V. Gunka, Y. Prysiazhnyi, Y. Hrynchuk, Iurii Sidun, Yuriy Demchuk, O. Shyshchak
The possibility of petroleum residues (tar and oxidized bitumen) modification with formaldehyde (37 % aqueous solution) has been studied at the temperature of 393±3 K for 3 h in the presence of organic solvent and using hydrochloric acid as a catalyst. Toluene, p-xylene, naphta solvent and n-octane were used as the solvents in the amount of 0–40 wt % relative to the initial material. By means of IR spectroscopy the resin-like compounds affecting the operational properties of petroleum residues have been detected. These compounds are formed as a result of formaldehyde reaction with residue components and solvent molecules.
{"title":"Production of Bitumen Modified with Low-Molecular Organic Compounds from Petroleum Residues. 1. Effect of Solvent Nature on the Properties of Petroleum Residues Modified with Folmaldehyde","authors":"M. Bratychak, V. Gunka, Y. Prysiazhnyi, Y. Hrynchuk, Iurii Sidun, Yuriy Demchuk, O. Shyshchak","doi":"10.23939/CHCHT15.02.274","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.274","url":null,"abstract":"The possibility of petroleum residues (tar and oxidized bitumen) modification with formaldehyde (37 % aqueous solution) has been studied at the temperature of 393±3 K for 3 h in the presence of organic solvent and using hydrochloric acid as a catalyst. Toluene, p-xylene, naphta solvent and n-octane were used as the solvents in the amount of 0–40 wt % relative to the initial material. By means of IR spectroscopy the resin-like compounds affecting the operational properties of petroleum residues have been detected. These compounds are formed as a result of formaldehyde reaction with residue components and solvent molecules.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74042782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this work, the green polymerization of vinyl acetate is carried out by a new method which consists in the use of clay called Maghnite-Na+ as an ecological catalyst, non-toxic, inexpensive and recyclable by a simple filtration. X-ray diffraction and scanning electron microscopy showed that Maghnite-Na+ is successfully obtained after cationic treatment (sodium) on crude maghnite. It is an effective alternative to replace toxic catalysts such as benzoyl peroxide and azobisisobutyronitrile which are mostly used during the synthesis of polyvinyl acetate (PVAc) making the polymerization reaction less problematic for the environment. The synthesis reaction is less energetic by the use of recycled polyurethane as a container for the reaction mixture and is considered as a renewable material and a good thermal insulator maintaining the temperature of 273 K for 6 h. The reaction in bulk is also preferred to avoid the use of a solvent and therefore to stay in the context of green chemistry. In these conditions, the structure of obtained polymer is established by 1H NMR and 13C NMR. Infrared spectroscopy (FT-IR) was also used to confirm the structure of PVAc. Thermogravimetric analysis showed that it is thermally stable and starts to degrade at 603 K while differential scanning calorimetry showed that this polymer has a glass transition temperature Tg of 323 K.
在这项工作中，醋酸乙烯酯的绿色聚合是通过一种新的方法进行的，该方法包括使用一种名为Maghnite-Na+的粘土作为生态催化剂，无毒，廉价，通过简单的过滤可回收。x射线衍射和扫描电镜结果表明，对粗磁铁矿进行阳离子(钠)处理后，获得了镁铁- na +。它是一种有效的替代品，可以取代在合成聚氯乙烯(PVAc)时常用的过氧化苯甲酰和偶氮二异丁腈等有毒催化剂，使聚合反应对环境的影响更小。使用回收聚氨酯作为反应混合物的容器，合成反应的能量较低，被认为是一种可再生材料和良好的隔热材料，可以保持273 K的温度6小时。散装反应也更适合避免使用溶剂，从而保持在绿色化学的背景下。在此条件下，通过1H NMR和13C NMR确定了所得聚合物的结构。红外光谱(FT-IR)也被用于确定聚氯乙烯的结构。热重分析表明该聚合物热稳定，在603 K时开始降解，差示扫描量热分析表明该聚合物的玻璃化转变温度Tg为323 K。
{"title":"Green Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst","authors":"Badia Imene Cherifi, M. Belbachir, S. Bennabi","doi":"10.23939/CHCHT15.02.183","DOIUrl":"https://doi.org/10.23939/CHCHT15.02.183","url":null,"abstract":"In this work, the green polymerization of vinyl acetate is carried out by a new method which consists in the use of clay called Maghnite-Na+ as an ecological catalyst, non-toxic, inexpensive and recyclable by a simple filtration. X-ray diffraction and scanning electron microscopy showed that Maghnite-Na+ is successfully obtained after cationic treatment (sodium) on crude maghnite. It is an effective alternative to replace toxic catalysts such as benzoyl peroxide and azobisisobutyronitrile which are mostly used during the synthesis of polyvinyl acetate (PVAc) making the polymerization reaction less problematic for the environment. The synthesis reaction is less energetic by the use of recycled polyurethane as a container for the reaction mixture and is considered as a renewable material and a good thermal insulator maintaining the temperature of 273 K for 6 h. The reaction in bulk is also preferred to avoid the use of a solvent and therefore to stay in the context of green chemistry. In these conditions, the structure of obtained polymer is established by 1H NMR and 13C NMR. Infrared spectroscopy (FT-IR) was also used to confirm the structure of PVAc. Thermogravimetric analysis showed that it is thermally stable and starts to degrade at 603 K while differential scanning calorimetry showed that this polymer has a glass transition temperature Tg of 323 K.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88022786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ab initio calculations based on the density functional theory were used. A cluster model of the faujasite zeolite structure (Al2Si22O66H36) with metal particles adsorbed above the aluminium centres was used. The NO and NH3 adsorption processes, individual and co-adsorption, have been studied over metal nanoparticles bound into zeolite clusters. Several configurations, electronic structure (charges, bond orders) and vibration frequencies have been analyzed to determine feasible pathways for the deNOx reaction. The M2O dimers (M = Cu, Mn or Fe) were considered in relation to the previous studies of iron complexes.
{"title":"Theoretical Studies of DENOx SCR over Cu-, Fe- and Mn-FAU Catalysts","authors":"Izabela Kurzydym, I. Czekaj","doi":"10.23939/CHCHT15.01.016","DOIUrl":"https://doi.org/10.23939/CHCHT15.01.016","url":null,"abstract":"Ab initio calculations based on the density functional theory were used. A cluster model of the faujasite zeolite structure (Al2Si22O66H36) with metal particles adsorbed above the aluminium centres was used. The NO and NH3 adsorption processes, individual and co-adsorption, have been studied over metal nanoparticles bound into zeolite clusters. Several configurations, electronic structure (charges, bond orders) and vibration frequencies have been analyzed to determine feasible pathways for the deNOx reaction. The M2O dimers (M = Cu, Mn or Fe) were considered in relation to the previous studies of iron complexes.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84074282","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Tokareva, Halyna Ohar, S. Tokarev, Yu Stetsyshyn
A new approach to synthesis at the aminated glass surface of novel biocompatible polymeric nanolayers consisting of poly(N-methacryloyl-L-proline) brushes has been developed. Formation of the polymer nanolayers has been realized in several stages. At the first stage, the glass surface has been modified by aminosilane (APTEC), afterwards monolayer of the peroxide-containing initiator (PI) based on pyromellitic acid has been tethered to this aminated surface. The immobilized PI has been used further for initiation of the grafting "from the surface" polymerization of N-methacryloyl-L-proline for obtaining of the peptidomimetic polymer brushes. Features of the reactions, as well as optimal conditions for performing the process are highlighted in this work. Presented here poly(N-methacryloyl-L-proline) grafted brush coatings are promising material for numerous applications in nanomedicine, especially for production of implants and systems of the controlled interaction with proteins and cells.
{"title":"Synthesis, Structure and Properties of the Grafted Peptidomimetic Polymer Brushes Based on Poly(N-methacryloyl-L-proline)","authors":"M. Tokareva, Halyna Ohar, S. Tokarev, Yu Stetsyshyn","doi":"10.23939/CHCHT15.01.026","DOIUrl":"https://doi.org/10.23939/CHCHT15.01.026","url":null,"abstract":"A new approach to synthesis at the aminated glass surface of novel biocompatible polymeric nanolayers consisting of poly(N-methacryloyl-L-proline) brushes has been developed. Formation of the polymer nanolayers has been realized in several stages. At the first stage, the glass surface has been modified by aminosilane (APTEC), afterwards monolayer of the peroxide-containing initiator (PI) based on pyromellitic acid has been tethered to this aminated surface. The immobilized PI has been used further for initiation of the grafting \"from the surface\" polymerization of N-methacryloyl-L-proline for obtaining of the peptidomimetic polymer brushes. Features of the reactions, as well as optimal conditions for performing the process are highlighted in this work. Presented here poly(N-methacryloyl-L-proline) grafted brush coatings are promising material for numerous applications in nanomedicine, especially for production of implants and systems of the controlled interaction with proteins and cells.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76956147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Influence of different types of surfactants on electrodeposition of copper- and carbon-bearing (graphite, carbon nanotubes (CNTs)) composite powder has been experimentally investigated. The size of powder particles decreased, and corrosion resistance increased when surfactants were added. Addition of cationic surfactant CTAB to the electrolyte with simultaneous ultrasonic treatment for CNTs dispersion gives maximum effect.
{"title":"Influence of Surfactants on Copper-CNTs Electrodeposition","authors":"I. Roslyk, Ganna Stovpchenkoko, G. Galchenko","doi":"10.23939/CHCHT15.01.125","DOIUrl":"https://doi.org/10.23939/CHCHT15.01.125","url":null,"abstract":"Influence of different types of surfactants on electrodeposition of copper- and carbon-bearing (graphite, carbon nanotubes (CNTs)) composite powder has been experimentally investigated. The size of powder particles decreased, and corrosion resistance increased when surfactants were added. Addition of cationic surfactant CTAB to the electrolyte with simultaneous ultrasonic treatment for CNTs dispersion gives maximum effect.","PeriodicalId":9793,"journal":{"name":"Chemistry & Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2021-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89618511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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