Objective: The objective of this study is to conduct a comparative investigation into the performance of multiwall carbon nanotube (MWCNT) and carbon wastes (C-waste) derived from the aluminum industry in the creation of thermally stable cementitious mortar. Specifically, the research aims to assess their impact on compressive strength and thermal stability, with a focus on identifying the superior additive for enhancing the properties of cement mortar. Methods: Cement mortar is produced using a blend of CEMIII cement and sand passing through a 1 mm sieve. Various ratios of MWCNT and C-waste, ranging from 0.1% to 0.7%, are incorporated into the mixture. Compressive strength tests are conducted at different intervals, up to 90 days, to evaluate the effects of additives on strength enhancement. Additionally, the resistance to high temperatures is examined by subjecting the mortar samples to firing temperatures up to 700 degrees Celsius. Results: The inclusion of both MWCNT and C-waste leads to improvements in compressive strength values, with the most significant enhancement observed at 0.1% concentration, resulting in approximately 70MPa and 75MPa at 90 days, respectively. Notably, C-waste demonstrates superior physical and mechanical properties compared to MWCNT, along with a lower production cost. Moreover, both additives exceed the specified limits for thermal resistance in mortar, achieving measurements of about 60MPa for MWCNT and 63MPa for C-waste when exposed to firing temperatures of 700 degrees Celsius. These results highlight the higher thermal stability of C-waste relative to MWCNT. Conclusion: In conclusion, this study confirms the efficacy of utilizing C-waste as an additive in cementitious mortar production, showcasing its superior performance over MWCNT in terms of compressive strength enhancement and thermal stability. The findings underscore the potential of repurposing industrial by-products such as C-waste to improve material properties while also addressing environmental concerns and reducing production costs in construction applications.
{"title":"Comparative Study between Multiwall Carbon Nano Tube and Carbon Waste from Aluminium Production in the Preparation of Thermally Stable Cementitious Mortar","authors":"Hisham M. Khater, Mahmoud Gharieb","doi":"10.53964/jmpcm.2024002","DOIUrl":"https://doi.org/10.53964/jmpcm.2024002","url":null,"abstract":"Objective: The objective of this study is to conduct a comparative investigation into the performance of multiwall carbon nanotube (MWCNT) and carbon wastes (C-waste) derived from the aluminum industry in the creation of thermally stable cementitious mortar. Specifically, the research aims to assess their impact on compressive strength and thermal stability, with a focus on identifying the superior additive for enhancing the properties of cement mortar. Methods: Cement mortar is produced using a blend of CEMIII cement and sand passing through a 1 mm sieve. Various ratios of MWCNT and C-waste, ranging from 0.1% to 0.7%, are incorporated into the mixture. Compressive strength tests are conducted at different intervals, up to 90 days, to evaluate the effects of additives on strength enhancement. Additionally, the resistance to high temperatures is examined by subjecting the mortar samples to firing temperatures up to 700 degrees Celsius. Results: The inclusion of both MWCNT and C-waste leads to improvements in compressive strength values, with the most significant enhancement observed at 0.1% concentration, resulting in approximately 70MPa and 75MPa at 90 days, respectively. Notably, C-waste demonstrates superior physical and mechanical properties compared to MWCNT, along with a lower production cost. Moreover, both additives exceed the specified limits for thermal resistance in mortar, achieving measurements of about 60MPa for MWCNT and 63MPa for C-waste when exposed to firing temperatures of 700 degrees Celsius. These results highlight the higher thermal stability of C-waste relative to MWCNT. Conclusion: In conclusion, this study confirms the efficacy of utilizing C-waste as an additive in cementitious mortar production, showcasing its superior performance over MWCNT in terms of compressive strength enhancement and thermal stability. The findings underscore the potential of repurposing industrial by-products such as C-waste to improve material properties while also addressing environmental concerns and reducing production costs in construction applications.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140996658","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}
Innovative energy storage devices, viz., supercapacitors and rechargeable batteries are of great awareness owing to their comprehensive claims in flexible electronics and implantations. In simple electronic devices, frequently facing problems like bending, collision, steeping, piercing, and even encountering shearing, fire, water, etc. Hence, a high mandate is needed for the constructive and consistency of energy storage devices. Hydrogels are hydrophilic three-dimensional polymers filled with water which are highly noticeable electrolyte materials due to their high-water permeability and smoothness, which enable them to fulfil the vital necessities for flexible energy storage devices. Hydrogels with intriguing physicochemical assets for justifiable energy storing for water production. The proposal of novel hydrogel electrolytes for supercapacitors and batteries with electrochemical performances for imminent growth. The biopolymeric hydrogel electrolytes can be chosen as substitute materials for supercapacitors due to their decent ionic conductivity, no fluid seepage, and no toxicity. Focus of the review aims to highlight the hydrogels materials combined into batteries and deliver thrilling tailorable architectures for multifunctionalities with amicable applications.
{"title":"Polymeric Hydrogels for Energy Devices","authors":"Selvam Guhanathan","doi":"10.53964/jmpcm.2024001","DOIUrl":"https://doi.org/10.53964/jmpcm.2024001","url":null,"abstract":"Innovative energy storage devices, viz., supercapacitors and rechargeable batteries are of great awareness owing to their comprehensive claims in flexible electronics and implantations. In simple electronic devices, frequently facing problems like bending, collision, steeping, piercing, and even encountering shearing, fire, water, etc. Hence, a high mandate is needed for the constructive and consistency of energy storage devices. Hydrogels are hydrophilic three-dimensional polymers filled with water which are highly noticeable electrolyte materials due to their high-water permeability and smoothness, which enable them to fulfil the vital necessities for flexible energy storage devices. Hydrogels with intriguing physicochemical assets for justifiable energy storing for water production. The proposal of novel hydrogel electrolytes for supercapacitors and batteries with electrochemical performances for imminent growth. The biopolymeric hydrogel electrolytes can be chosen as substitute materials for supercapacitors due to their decent ionic conductivity, no fluid seepage, and no toxicity. Focus of the review aims to highlight the hydrogels materials combined into batteries and deliver thrilling tailorable architectures for multifunctionalities with amicable applications.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140716814","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}
Mostafa Abbaszadeh Valojerdi, S. M. Zebarjad, M. H. Moghim
Objective: In the current research, the creep behavior of polyethylene (PE) matrix nanocomposites reinforced with different content of clay nano particles (i.e., 0, 1, 3, 5, 10wt%) at different temperatures (25 and 50℃) has been investigated. Methods: In order to produce composite samples of pure PE reinforced with different percentages of clay (0, 1, 3, 5 and 10% by weight), a twin extruder was used in the temperature range of 200-230℃. Also, to produce the standard samples, an injection machine was used using in the temperature range of 220-230℃. The samples were subjected to a constant load, typically around 0.7 to 0.8 times the yield strength, at 25 and 50℃ , and at constant strain rate of 0.1min-1. Results: The creep investigations showed that for PE and its nanocomposites the creep trend could be divided into primary, secondary, and tertiary stages. The length of each stage depended strongly on both temperature and the stress level at which the samples tested as well as the clay content. It was observed that adding nano particles in small amounts (1wt%) led to an increase in the length of the creep life of PE and it also improved this property in both temperatures. Conclusion: It was observed that increasing test temperature from causes to decrease the creep strength as well as a rapid onset of plastic deformation for all materials including PE and its nanocomposites. PE nanocomposites with higher than 1wt% clay exhibited a noticeable drop in creep strength particularly at 50℃.
{"title":"A Study on the Role of Clay Nanoparticles and Temperature on the Creep Behavior of Polyethylene Matrix Nanocomposite","authors":"Mostafa Abbaszadeh Valojerdi, S. M. Zebarjad, M. H. Moghim","doi":"10.53964/jmpcm.2023004","DOIUrl":"https://doi.org/10.53964/jmpcm.2023004","url":null,"abstract":"Objective: In the current research, the creep behavior of polyethylene (PE) matrix nanocomposites reinforced with different content of clay nano particles (i.e., 0, 1, 3, 5, 10wt%) at different temperatures (25 and 50℃) has been investigated. Methods: In order to produce composite samples of pure PE reinforced with different percentages of clay (0, 1, 3, 5 and 10% by weight), a twin extruder was used in the temperature range of 200-230℃. Also, to produce the standard samples, an injection machine was used using in the temperature range of 220-230℃. The samples were subjected to a constant load, typically around 0.7 to 0.8 times the yield strength, at 25 and 50℃ , and at constant strain rate of 0.1min-1. Results: The creep investigations showed that for PE and its nanocomposites the creep trend could be divided into primary, secondary, and tertiary stages. The length of each stage depended strongly on both temperature and the stress level at which the samples tested as well as the clay content. It was observed that adding nano particles in small amounts (1wt%) led to an increase in the length of the creep life of PE and it also improved this property in both temperatures. Conclusion: It was observed that increasing test temperature from causes to decrease the creep strength as well as a rapid onset of plastic deformation for all materials including PE and its nanocomposites. PE nanocomposites with higher than 1wt% clay exhibited a noticeable drop in creep strength particularly at 50℃.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139140152","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}
Beckley Victorine Namondo, Ekane Peter Etape, J. Foba-Tendo
Background: The presence of natural fiber in composites has shown a positive influence on the resilience of the reinforced polymer composites but this influence shows variability with Natural fiber Surface treatment, concentration of treatment solution and the length of treatment time. 5wt.% of sodium hydroxide (NaOH) alkali solution concentration has shown to be effective and efficient in dissolving the hemicellulose and the lignin portions while preserving the cellulose part of the fiber. There is enough literature on the chemical, physical, mechanical and thermal properties of Natural fibers but there is no comprehensive study on the chemical composition, morphology and concentration of the chemical compositions, water absorption behavior and thermal properties of Raffia hookeri fibers. Objective: Given that these properties vary with both the plant type and Botanical species, we are taking this advantage to study in detailed the morphological and composition of Raffia hookeri fiber and to Characterize the fiber for the evaluation of Mechanical Properties for Technological application. Methods: Raffia hookeri fiber was extracted and the basic technological application properties such as moisture and water adsorption, morphology, chemical, physical and thermal properties were analyzed using, chemical composition analysis, scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), Fourier transformed Infrared (FTIR), X-ray diffraction (XRD) and Thermo gravimetric analysis (TGA) while tensile test was used to evaluate the mechanical behavior of the fibers. Results: Chemical analysis revealed that the fiber was made up of cellulose (40wt.%), hemicellulose (20wt.%), lignin (33wt.%) and extractives 7wt.%, Thermal analysis indicated thermal stability up to 220oC, while the SEM/EDS results revealed that the effect of treatment on the fiber surface increased with the treatment time and reached maximum after 10h. This variability inferred on the morphological composition which recorded modifying effects both on the fiber-polymer matrix and the mechanical properties of the treated fibers. The FT-IR and XRD results indicated modification of the functional groups on the fiber morphology which improved on the mechanical, moisture and water adsorption capacity of the treated fibers. Conclusion: The alkali treatment has modifying effects on Raffia hookeri fiber morphology and chemical composition which affect its technological application Properties.
{"title":"Raffia hookeri Fiber: Effect of Alkali Treatment on Morphology, Composition and Technological Application Properties","authors":"Beckley Victorine Namondo, Ekane Peter Etape, J. Foba-Tendo","doi":"10.53964/jmpcm.2023003","DOIUrl":"https://doi.org/10.53964/jmpcm.2023003","url":null,"abstract":"Background: The presence of natural fiber in composites has shown a positive influence on the resilience of the reinforced polymer composites but this influence shows variability with Natural fiber Surface treatment, concentration of treatment solution and the length of treatment time. 5wt.% of sodium hydroxide (NaOH) alkali solution concentration has shown to be effective and efficient in dissolving the hemicellulose and the lignin portions while preserving the cellulose part of the fiber. There is enough literature on the chemical, physical, mechanical and thermal properties of Natural fibers but there is no comprehensive study on the chemical composition, morphology and concentration of the chemical compositions, water absorption behavior and thermal properties of Raffia hookeri fibers. Objective: Given that these properties vary with both the plant type and Botanical species, we are taking this advantage to study in detailed the morphological and composition of Raffia hookeri fiber and to Characterize the fiber for the evaluation of Mechanical Properties for Technological application. Methods: Raffia hookeri fiber was extracted and the basic technological application properties such as moisture and water adsorption, morphology, chemical, physical and thermal properties were analyzed using, chemical composition analysis, scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), Fourier transformed Infrared (FTIR), X-ray diffraction (XRD) and Thermo gravimetric analysis (TGA) while tensile test was used to evaluate the mechanical behavior of the fibers. Results: Chemical analysis revealed that the fiber was made up of cellulose (40wt.%), hemicellulose (20wt.%), lignin (33wt.%) and extractives 7wt.%, Thermal analysis indicated thermal stability up to 220oC, while the SEM/EDS results revealed that the effect of treatment on the fiber surface increased with the treatment time and reached maximum after 10h. This variability inferred on the morphological composition which recorded modifying effects both on the fiber-polymer matrix and the mechanical properties of the treated fibers. The FT-IR and XRD results indicated modification of the functional groups on the fiber morphology which improved on the mechanical, moisture and water adsorption capacity of the treated fibers. Conclusion: The alkali treatment has modifying effects on Raffia hookeri fiber morphology and chemical composition which affect its technological application Properties.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115120878","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}
Objective: This paper investigates a range of optimization approaches for advanced composite structural items made of polymers with inclusion of specially formulated glass fibers (GFs) (either continuous linear strands or mesh matrix). Methods: Ridged polymer test panels were tested for flexural strength using variable loads (ASTM D790 standard). Tested variables included: (a) thickness and amount of GF dispersed within polymer matrix, (b) addition and placement of open mesh woven element on open flat surfaces of polymer panel, and (c) addition and selective placement of tension setters on ridges. Results: Optimal amounts of additives, design and compositions were determined for strength and impact resistance of polymer composites. Tension setters were found to be best embedded in laterally extending rib elements of composite structure, preferably as end-portions of rib elements. Open mesh woven element should be placed strategically within polymeric body to provide impact strength where needed the most. Conclusion: These optimized composite structural designs showed higher strength (up to 331% of the base polymer), higher impact resistance (up to 551% of the base), with additional benefit of reduced weight by 15-21%, as compared to conventional polymer panels.
{"title":"Optimization Techniques for Multi-component Materials","authors":"Victor Vasnetsov, Catherine Vasnetsov","doi":"10.53964/jmpcm.2023002","DOIUrl":"https://doi.org/10.53964/jmpcm.2023002","url":null,"abstract":"Objective: This paper investigates a range of optimization approaches for advanced composite structural items made of polymers with inclusion of specially formulated glass fibers (GFs) (either continuous linear strands or mesh matrix). Methods: Ridged polymer test panels were tested for flexural strength using variable loads (ASTM D790 standard). Tested variables included: (a) thickness and amount of GF dispersed within polymer matrix, (b) addition and placement of open mesh woven element on open flat surfaces of polymer panel, and (c) addition and selective placement of tension setters on ridges. Results: Optimal amounts of additives, design and compositions were determined for strength and impact resistance of polymer composites. Tension setters were found to be best embedded in laterally extending rib elements of composite structure, preferably as end-portions of rib elements. Open mesh woven element should be placed strategically within polymeric body to provide impact strength where needed the most. Conclusion: These optimized composite structural designs showed higher strength (up to 331% of the base polymer), higher impact resistance (up to 551% of the base), with additional benefit of reduced weight by 15-21%, as compared to conventional polymer panels.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130254220","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}
Z. Zubair, M. Rizwan, Fatima Shehzadi, K. Shaker, Fiaz Hussain, H. F. Shakir
Objective: Glass fiber reinforced composites with epoxy were prepared using thermally reduced graphene oxide (TRGO) and multiwall carbon nanotubes (CNTs) as electrically conductive nano filler. Electrical, mechanical, dielectric and electromagnetic interference (EMI) shielding properties were analyzed and compared. Methods: TRGO was prepared by modified hummers method and X-ray diffraction spectra showed the carbon hexagonal structure with 6-8nm of thickness. Tensile, flexural and impact strength of these composites was comparable and increase with increasing filler content. The effect of TRGO and CNTs on AC & DC conductivity of composites was also compared, which showed that increasing the TRGO content increased the electrical conductivity little better than that of CNTs filled composite. Results: The dielectric properties also improved better for composite incorporating TRGO than with the CNTs, at higher frequency (5MHz). With addition of 2.0% TRGO and CNTs, the maximum SET observed was 32dB at lower frequency, with TRGO-based composite manage to maintain its performance even at higher frequency whereas, this value dropped to 24dB for CNT-based composite at 5MHz of frequency. Conclusion: The dispersion state, the composition of the fillers, and their interaction with matrix are the most important factors in these polymeric composites for the development in EMI shielding effectiveness.
{"title":"Electric, Dielectric, Mechanical and Emi Shielding Study of Fiber Reinforced Polymer Based Nanocomposites with the Incorporation of Graphene/Cnts","authors":"Z. Zubair, M. Rizwan, Fatima Shehzadi, K. Shaker, Fiaz Hussain, H. F. Shakir","doi":"10.53964/jmpcm.2023001","DOIUrl":"https://doi.org/10.53964/jmpcm.2023001","url":null,"abstract":"Objective: Glass fiber reinforced composites with epoxy were prepared using thermally reduced graphene oxide (TRGO) and multiwall carbon nanotubes (CNTs) as electrically conductive nano filler. Electrical, mechanical, dielectric and electromagnetic interference (EMI) shielding properties were analyzed and compared. Methods: TRGO was prepared by modified hummers method and X-ray diffraction spectra showed the carbon hexagonal structure with 6-8nm of thickness. Tensile, flexural and impact strength of these composites was comparable and increase with increasing filler content. The effect of TRGO and CNTs on AC & DC conductivity of composites was also compared, which showed that increasing the TRGO content increased the electrical conductivity little better than that of CNTs filled composite. Results: The dielectric properties also improved better for composite incorporating TRGO than with the CNTs, at higher frequency (5MHz). With addition of 2.0% TRGO and CNTs, the maximum SET observed was 32dB at lower frequency, with TRGO-based composite manage to maintain its performance even at higher frequency whereas, this value dropped to 24dB for CNT-based composite at 5MHz of frequency. Conclusion: The dispersion state, the composition of the fillers, and their interaction with matrix are the most important factors in these polymeric composites for the development in EMI shielding effectiveness.","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115796989","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}
{"title":"Hexagonal Lead Ferrite Magnetic Separation Catalysts: Synthesis, Optical Characterization, Ultrasonic Catalytic Activity and Performance Prediction","authors":"","doi":"10.53964/jmpcm.2022011","DOIUrl":"https://doi.org/10.53964/jmpcm.2022011","url":null,"abstract":"","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125142498","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}
Objective: The objective of the current work is to synthesize the conducting polymer, i.e
目的:本研究的目的是合成导电聚合物，即导电聚合物
{"title":"Effect of Deposition Time on Electrochemical Properties of Polyaniline Samples Prepared by Chemical Bath Deposition","authors":"S. P. Thokale, B. Lokhande","doi":"10.53964/jmpcm.2022010","DOIUrl":"https://doi.org/10.53964/jmpcm.2022010","url":null,"abstract":"Objective: The objective of the current work is to synthesize the conducting polymer, i.e","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116867555","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}
{"title":"Solutions Containing Polyvinylpyrrolidone for the Production of TiO2 Fibers Used As Semiconductors in the Photodegradation of Two Different Dyes","authors":"","doi":"10.53964/jmpcm.2022009","DOIUrl":"https://doi.org/10.53964/jmpcm.2022009","url":null,"abstract":"","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123362615","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}
{"title":"A Green Method for Preparing Thioctic Acid Hydrogel at Room Temperature","authors":"","doi":"10.53964/jmpcm.2022008","DOIUrl":"https://doi.org/10.53964/jmpcm.2022008","url":null,"abstract":"","PeriodicalId":385339,"journal":{"name":"Journal of Modern Polymer Chemistry and Materials","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126638322","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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