Ljerka Kratofil Krehula, Ana Peršić, N. Popov, S. Krehula
Due to the intensive search for new types of advanced polymer materials for targeted applications, this work offers insight into the properties of low-density polyethylene/hematite composites. The specific feature of this study lies in the use of elongated hematite particles of different shapes. Uniform ellipsoid-, peanut- and rod-shaped hematite particles were hydrothermally synthesized and incorporated into the polymer matrix of low-density polyethylene (LDPE). LDPE/hematite composites are prepared by melt mixing. Hematite particles are characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (PXRD). The pure LDPE polymer and LDPE/hematite composites were studied by FT-IR and UV-Vis-NIR spectroscopy and by thermogravimetric analysis (TGA). The determination of the mechanical and barrier properties was also carried out. The obtained results indicate the influence of the elongated particles on the improvement of LDPE properties. An increase in thermal stability and UV-absorption was observed as well as the improvement of mechanical and barrier properties. The improvement of the composites’ properties in comparison to the pure LDPE is especially visible in the composites prepared with low content of hematite (0.25%). LDPE/hematite composites have promising characteristics for application as packaging materials with enhanced mechanical, thermal and barrier properties as well as UV-protective materials.
随着对新型先进聚合物材料目标应用的深入研究，本研究对低密度聚乙烯/赤铁矿复合材料的性能进行了深入探讨。这项研究的特点在于使用了不同形状的细长赤铁矿颗粒。通过水热法合成了均匀的椭圆形、花生形和棒状赤铁矿颗粒，并将其加入到低密度聚乙烯（LDPE）的聚合物基体中。低密度聚乙烯/赤铁矿复合材料是通过熔融混合制备的。赤铁矿颗粒通过扫描电子显微镜（SEM）和粉末 X 射线衍射（PXRD）进行表征。纯低密度聚乙烯聚合物和低密度聚乙烯/赤铁矿复合材料通过傅立叶变换红外光谱、紫外-可见-近红外光谱和热重分析（TGA）进行了研究。此外，还对机械性能和阻隔性能进行了测定。结果表明，细长颗粒对改善低密度聚乙烯的性能有一定影响。热稳定性和紫外线吸收率都有所提高，机械性能和阻隔性能也有所改善。在赤铁矿含量较低（0.25%）的复合材料中，与纯低密度聚乙烯相比，复合材料性能的改善尤为明显。低密度聚乙烯/赤铁矿复合材料具有良好的机械、热和阻隔性能，可用作包装材料和紫外线防护材料。
{"title":"Polymer Composites of Low-Density Polyethylene (LDPE) with Elongated Hematite (α-Fe2O3) Particles of Different Shapes","authors":"Ljerka Kratofil Krehula, Ana Peršić, N. Popov, S. Krehula","doi":"10.3390/jcs8020073","DOIUrl":"https://doi.org/10.3390/jcs8020073","url":null,"abstract":"Due to the intensive search for new types of advanced polymer materials for targeted applications, this work offers insight into the properties of low-density polyethylene/hematite composites. The specific feature of this study lies in the use of elongated hematite particles of different shapes. Uniform ellipsoid-, peanut- and rod-shaped hematite particles were hydrothermally synthesized and incorporated into the polymer matrix of low-density polyethylene (LDPE). LDPE/hematite composites are prepared by melt mixing. Hematite particles are characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (PXRD). The pure LDPE polymer and LDPE/hematite composites were studied by FT-IR and UV-Vis-NIR spectroscopy and by thermogravimetric analysis (TGA). The determination of the mechanical and barrier properties was also carried out. The obtained results indicate the influence of the elongated particles on the improvement of LDPE properties. An increase in thermal stability and UV-absorption was observed as well as the improvement of mechanical and barrier properties. The improvement of the composites’ properties in comparison to the pure LDPE is especially visible in the composites prepared with low content of hematite (0.25%). LDPE/hematite composites have promising characteristics for application as packaging materials with enhanced mechanical, thermal and barrier properties as well as UV-protective materials.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"44 21","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139845413","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}
D. Dimonie, R. Grigorescu, B. Trică, C. Damian, Eugeniu Vasile, Roxana Trusca, Cristian-Andi Nicolae, Diana Constantinescu-Aruxandei, F. Oancea
This article compares two exfoliation options of multilayered silicate, one considering the action of shear stress and temperature during melt compounding and another takeing into account the action of the thermo-mechanical pretreatment of multilayered silicate in a plasticizer common to the starch and polyvinyl alcohol (PVOH), the two polymers from the compound. Increasing the action time of the shear stress and temperature during melt compounding proved to be an ineffective method for silicate exfoliation following the high degradability of starch and PVOH under thermo-mechanical conditions and the loss of hydration of the multilayered silicate under thermo-mechanical conditions. The obtained results prove that, by pretreating before embedding into the desired starch-PVOH matrix, it was possible to cancel the electrostatic attractions between the component lamellae of a multilayered silicate. During melt compounding with the two polymers, new attractions between the obtained lamellae and the polar groups of each polymer from the blend were settled, and so, without the usage of a liquid plasticizer, exfoliated intercalated nanocomposites were achieved. The improved properties and the practical importance of the new nanocomposites regards the obtaining of a non-degradable material that has a white color, better elastic properties and thermal stability, and a higher dissipation capacity of deformation energy.
{"title":"Increasing the Efficiency of Multilayered Silicate Melt Incorporation into Starch-Based Polymeric Matrices","authors":"D. Dimonie, R. Grigorescu, B. Trică, C. Damian, Eugeniu Vasile, Roxana Trusca, Cristian-Andi Nicolae, Diana Constantinescu-Aruxandei, F. Oancea","doi":"10.3390/jcs8020072","DOIUrl":"https://doi.org/10.3390/jcs8020072","url":null,"abstract":"This article compares two exfoliation options of multilayered silicate, one considering the action of shear stress and temperature during melt compounding and another takeing into account the action of the thermo-mechanical pretreatment of multilayered silicate in a plasticizer common to the starch and polyvinyl alcohol (PVOH), the two polymers from the compound. Increasing the action time of the shear stress and temperature during melt compounding proved to be an ineffective method for silicate exfoliation following the high degradability of starch and PVOH under thermo-mechanical conditions and the loss of hydration of the multilayered silicate under thermo-mechanical conditions. The obtained results prove that, by pretreating before embedding into the desired starch-PVOH matrix, it was possible to cancel the electrostatic attractions between the component lamellae of a multilayered silicate. During melt compounding with the two polymers, new attractions between the obtained lamellae and the polar groups of each polymer from the blend were settled, and so, without the usage of a liquid plasticizer, exfoliated intercalated nanocomposites were achieved. The improved properties and the practical importance of the new nanocomposites regards the obtaining of a non-degradable material that has a white color, better elastic properties and thermal stability, and a higher dissipation capacity of deformation energy.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"107 25","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139786069","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}
D. Dimonie, R. Grigorescu, B. Trică, C. Damian, Eugeniu Vasile, Roxana Trusca, Cristian-Andi Nicolae, Diana Constantinescu-Aruxandei, F. Oancea
This article compares two exfoliation options of multilayered silicate, one considering the action of shear stress and temperature during melt compounding and another takeing into account the action of the thermo-mechanical pretreatment of multilayered silicate in a plasticizer common to the starch and polyvinyl alcohol (PVOH), the two polymers from the compound. Increasing the action time of the shear stress and temperature during melt compounding proved to be an ineffective method for silicate exfoliation following the high degradability of starch and PVOH under thermo-mechanical conditions and the loss of hydration of the multilayered silicate under thermo-mechanical conditions. The obtained results prove that, by pretreating before embedding into the desired starch-PVOH matrix, it was possible to cancel the electrostatic attractions between the component lamellae of a multilayered silicate. During melt compounding with the two polymers, new attractions between the obtained lamellae and the polar groups of each polymer from the blend were settled, and so, without the usage of a liquid plasticizer, exfoliated intercalated nanocomposites were achieved. The improved properties and the practical importance of the new nanocomposites regards the obtaining of a non-degradable material that has a white color, better elastic properties and thermal stability, and a higher dissipation capacity of deformation energy.
{"title":"Increasing the Efficiency of Multilayered Silicate Melt Incorporation into Starch-Based Polymeric Matrices","authors":"D. Dimonie, R. Grigorescu, B. Trică, C. Damian, Eugeniu Vasile, Roxana Trusca, Cristian-Andi Nicolae, Diana Constantinescu-Aruxandei, F. Oancea","doi":"10.3390/jcs8020072","DOIUrl":"https://doi.org/10.3390/jcs8020072","url":null,"abstract":"This article compares two exfoliation options of multilayered silicate, one considering the action of shear stress and temperature during melt compounding and another takeing into account the action of the thermo-mechanical pretreatment of multilayered silicate in a plasticizer common to the starch and polyvinyl alcohol (PVOH), the two polymers from the compound. Increasing the action time of the shear stress and temperature during melt compounding proved to be an ineffective method for silicate exfoliation following the high degradability of starch and PVOH under thermo-mechanical conditions and the loss of hydration of the multilayered silicate under thermo-mechanical conditions. The obtained results prove that, by pretreating before embedding into the desired starch-PVOH matrix, it was possible to cancel the electrostatic attractions between the component lamellae of a multilayered silicate. During melt compounding with the two polymers, new attractions between the obtained lamellae and the polar groups of each polymer from the blend were settled, and so, without the usage of a liquid plasticizer, exfoliated intercalated nanocomposites were achieved. The improved properties and the practical importance of the new nanocomposites regards the obtaining of a non-degradable material that has a white color, better elastic properties and thermal stability, and a higher dissipation capacity of deformation energy.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"45 19","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139846116","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}
Ljerka Kratofil Krehula, Ana Peršić, N. Popov, S. Krehula
Due to the intensive search for new types of advanced polymer materials for targeted applications, this work offers insight into the properties of low-density polyethylene/hematite composites. The specific feature of this study lies in the use of elongated hematite particles of different shapes. Uniform ellipsoid-, peanut- and rod-shaped hematite particles were hydrothermally synthesized and incorporated into the polymer matrix of low-density polyethylene (LDPE). LDPE/hematite composites are prepared by melt mixing. Hematite particles are characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (PXRD). The pure LDPE polymer and LDPE/hematite composites were studied by FT-IR and UV-Vis-NIR spectroscopy and by thermogravimetric analysis (TGA). The determination of the mechanical and barrier properties was also carried out. The obtained results indicate the influence of the elongated particles on the improvement of LDPE properties. An increase in thermal stability and UV-absorption was observed as well as the improvement of mechanical and barrier properties. The improvement of the composites’ properties in comparison to the pure LDPE is especially visible in the composites prepared with low content of hematite (0.25%). LDPE/hematite composites have promising characteristics for application as packaging materials with enhanced mechanical, thermal and barrier properties as well as UV-protective materials.
随着对新型先进聚合物材料目标应用的深入研究，本研究对低密度聚乙烯/赤铁矿复合材料的性能进行了深入探讨。这项研究的特点在于使用了不同形状的细长赤铁矿颗粒。通过水热法合成了均匀的椭圆形、花生形和棒状赤铁矿颗粒，并将其加入到低密度聚乙烯（LDPE）的聚合物基体中。低密度聚乙烯/赤铁矿复合材料是通过熔融混合制备的。赤铁矿颗粒通过扫描电子显微镜（SEM）和粉末 X 射线衍射（PXRD）进行表征。纯低密度聚乙烯聚合物和低密度聚乙烯/赤铁矿复合材料通过傅立叶变换红外光谱、紫外-可见-近红外光谱和热重分析（TGA）进行了研究。此外，还对机械性能和阻隔性能进行了测定。结果表明，细长颗粒对改善低密度聚乙烯的性能有一定影响。热稳定性和紫外线吸收率都有所提高，机械性能和阻隔性能也有所改善。在赤铁矿含量较低（0.25%）的复合材料中，与纯低密度聚乙烯相比，复合材料性能的改善尤为明显。低密度聚乙烯/赤铁矿复合材料具有良好的机械、热和阻隔性能，可用作包装材料和紫外线防护材料。
{"title":"Polymer Composites of Low-Density Polyethylene (LDPE) with Elongated Hematite (α-Fe2O3) Particles of Different Shapes","authors":"Ljerka Kratofil Krehula, Ana Peršić, N. Popov, S. Krehula","doi":"10.3390/jcs8020073","DOIUrl":"https://doi.org/10.3390/jcs8020073","url":null,"abstract":"Due to the intensive search for new types of advanced polymer materials for targeted applications, this work offers insight into the properties of low-density polyethylene/hematite composites. The specific feature of this study lies in the use of elongated hematite particles of different shapes. Uniform ellipsoid-, peanut- and rod-shaped hematite particles were hydrothermally synthesized and incorporated into the polymer matrix of low-density polyethylene (LDPE). LDPE/hematite composites are prepared by melt mixing. Hematite particles are characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (PXRD). The pure LDPE polymer and LDPE/hematite composites were studied by FT-IR and UV-Vis-NIR spectroscopy and by thermogravimetric analysis (TGA). The determination of the mechanical and barrier properties was also carried out. The obtained results indicate the influence of the elongated particles on the improvement of LDPE properties. An increase in thermal stability and UV-absorption was observed as well as the improvement of mechanical and barrier properties. The improvement of the composites’ properties in comparison to the pure LDPE is especially visible in the composites prepared with low content of hematite (0.25%). LDPE/hematite composites have promising characteristics for application as packaging materials with enhanced mechanical, thermal and barrier properties as well as UV-protective materials.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"112 20","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139785329","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. Lesbayev, Nurgali Rakhymzhan, Gaukhar Ustayeva, Yerkebulan Maral, M. Atamanov, Moldir Auyelkhankyzy, Ayazhan Zhamash
This study proposes a method to control the pore-forming process by performing preliminary mechanical activation of the initial rice husk before carbonization. Preliminary mechanical activation of the initial rice husk leads to the loosening of the intercellular substance and its partial depolymerization, thereby increasing the availability of its internal structure for pore formation during carbonization and chemical activation. Using the method described above, nanoporous carbon was obtained with a Brunauer–Emmett–Teller (BET)-calculated specific surface area of 2713 m2/g, a micropore specific surface area calculated by using the Dubinina–Radushkevich (D-R) method of 3099 m2/g, and a total pore volume calculated by using the Barett–Joyner–Halenda (BJH) method of 1.625 cm3/g. Due to these characteristics, the adsorption capacity in the obtained sample was for hydrogen 3.7 wt.% at a temperature of −190 °C and a pressure of 9 kgf/cm2, which is 29.7% higher than the adsorption capacity of nanoporous carbon obtained based on rice husk without mechanical activation. The composite “carbon–platinum” NC-2/Pt10%, at a temperature of 20 °C and a pressure of 9 kgf/cm2, showed an increase in sorption capacity of 27% compared to pure nanoporous carbon NC-2, which is explained by the emergence of the spillover effect.
{"title":"Preparation of Nanoporous Carbon from Rice Husk with Improved Textural Characteristics for Hydrogen Sorption","authors":"B. Lesbayev, Nurgali Rakhymzhan, Gaukhar Ustayeva, Yerkebulan Maral, M. Atamanov, Moldir Auyelkhankyzy, Ayazhan Zhamash","doi":"10.3390/jcs8020074","DOIUrl":"https://doi.org/10.3390/jcs8020074","url":null,"abstract":"This study proposes a method to control the pore-forming process by performing preliminary mechanical activation of the initial rice husk before carbonization. Preliminary mechanical activation of the initial rice husk leads to the loosening of the intercellular substance and its partial depolymerization, thereby increasing the availability of its internal structure for pore formation during carbonization and chemical activation. Using the method described above, nanoporous carbon was obtained with a Brunauer–Emmett–Teller (BET)-calculated specific surface area of 2713 m2/g, a micropore specific surface area calculated by using the Dubinina–Radushkevich (D-R) method of 3099 m2/g, and a total pore volume calculated by using the Barett–Joyner–Halenda (BJH) method of 1.625 cm3/g. Due to these characteristics, the adsorption capacity in the obtained sample was for hydrogen 3.7 wt.% at a temperature of −190 °C and a pressure of 9 kgf/cm2, which is 29.7% higher than the adsorption capacity of nanoporous carbon obtained based on rice husk without mechanical activation. The composite “carbon–platinum” NC-2/Pt10%, at a temperature of 20 °C and a pressure of 9 kgf/cm2, showed an increase in sorption capacity of 27% compared to pure nanoporous carbon NC-2, which is explained by the emergence of the spillover effect.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"118 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139785571","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. Lesbayev, Nurgali Rakhymzhan, Gaukhar Ustayeva, Yerkebulan Maral, M. Atamanov, Moldir Auyelkhankyzy, Ayazhan Zhamash
This study proposes a method to control the pore-forming process by performing preliminary mechanical activation of the initial rice husk before carbonization. Preliminary mechanical activation of the initial rice husk leads to the loosening of the intercellular substance and its partial depolymerization, thereby increasing the availability of its internal structure for pore formation during carbonization and chemical activation. Using the method described above, nanoporous carbon was obtained with a Brunauer–Emmett–Teller (BET)-calculated specific surface area of 2713 m2/g, a micropore specific surface area calculated by using the Dubinina–Radushkevich (D-R) method of 3099 m2/g, and a total pore volume calculated by using the Barett–Joyner–Halenda (BJH) method of 1.625 cm3/g. Due to these characteristics, the adsorption capacity in the obtained sample was for hydrogen 3.7 wt.% at a temperature of −190 °C and a pressure of 9 kgf/cm2, which is 29.7% higher than the adsorption capacity of nanoporous carbon obtained based on rice husk without mechanical activation. The composite “carbon–platinum” NC-2/Pt10%, at a temperature of 20 °C and a pressure of 9 kgf/cm2, showed an increase in sorption capacity of 27% compared to pure nanoporous carbon NC-2, which is explained by the emergence of the spillover effect.
{"title":"Preparation of Nanoporous Carbon from Rice Husk with Improved Textural Characteristics for Hydrogen Sorption","authors":"B. Lesbayev, Nurgali Rakhymzhan, Gaukhar Ustayeva, Yerkebulan Maral, M. Atamanov, Moldir Auyelkhankyzy, Ayazhan Zhamash","doi":"10.3390/jcs8020074","DOIUrl":"https://doi.org/10.3390/jcs8020074","url":null,"abstract":"This study proposes a method to control the pore-forming process by performing preliminary mechanical activation of the initial rice husk before carbonization. Preliminary mechanical activation of the initial rice husk leads to the loosening of the intercellular substance and its partial depolymerization, thereby increasing the availability of its internal structure for pore formation during carbonization and chemical activation. Using the method described above, nanoporous carbon was obtained with a Brunauer–Emmett–Teller (BET)-calculated specific surface area of 2713 m2/g, a micropore specific surface area calculated by using the Dubinina–Radushkevich (D-R) method of 3099 m2/g, and a total pore volume calculated by using the Barett–Joyner–Halenda (BJH) method of 1.625 cm3/g. Due to these characteristics, the adsorption capacity in the obtained sample was for hydrogen 3.7 wt.% at a temperature of −190 °C and a pressure of 9 kgf/cm2, which is 29.7% higher than the adsorption capacity of nanoporous carbon obtained based on rice husk without mechanical activation. The composite “carbon–platinum” NC-2/Pt10%, at a temperature of 20 °C and a pressure of 9 kgf/cm2, showed an increase in sorption capacity of 27% compared to pure nanoporous carbon NC-2, which is explained by the emergence of the spillover effect.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"18 11","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139845684","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}
Sergey V. Yudintsev, Michael I. Ojovan, V. Malkovsky
The current policy of managing high-level waste (HLW) derived in the closed nuclear fuel cycle consists in their vitrification into B-Si or Al-P vitreous forms. These compounds have rather limited capacity with respect to the HLW (5–20 wt%), and their properties change over time due to devitrification of the glasses. Cardinal improvement in the management of HLW can be achieved by their separation onto groups of elements with similar properties, followed by their immobilization in robust waste forms (matrices) and emplacement in deep disposal facilities. One of the possible fractions contains trivalent rare-earth elements (REEs) and minor actinides (MAs = Am and Cm). REEs are the fission products of actinides, which are mainly represented by stable isotopes of elements from La to Gd as well as Y. This group also contains small amounts of short-lived radionuclides with half-lives (T1/2) from 284 days (144Ce) to 90 years (151Sm), including 147Pm (T1/2 = 2.6 years), 154Eu (T1/2 = 8.8 years), and 155Eu (T1/2 = 5 years). However, the main long-term environmental hazard of the REE–MA fraction is associated with Am and Cm, with half-lives from 18 years (244Cm) to 8500 years (245Cm), and their daughter products: 237Np (T1/2 = 2.14 × 106 years), 239Pu (T1/2 = 2.41 × 104 years), 240Pu (T1/2 = 6537 years), and 242Pu (T1/2 = 3.76 × 105 years), which should be immobilized into a durable waste form that prevents their release into the environment. Due to the heat generated by decaying radionuclides, the temperature of matrices with an REE–MA fraction will be increased by hundreds of centigrade above ambient. This process can be utilized by selecting a vitreous waste form that will crystallize to form durable crystalline phases with long-lived radionuclides. We estimated the thermal effects in a potential REE–MA glass composite material based on the size of the block, the content of waste, the time of storage before immobilization and after disposal, and showed that it is possible to select the waste loading, size of blocks, and storage time so that the temperature of the matrix during the first decades will reach 500–700 °C, which corresponds to the optimal range of glass crystallization. As a result, a glass–ceramic composite will be produced that contains monazite ((REE,MA)PO4) in phosphate glasses; britholite (Cax(REE,MA)10-x(SiO4)6O2) or zirconolite ((Ca,REE,MA)(Zr,REE,MA)(Ti,Al,Fe)2O7), in silicate systems. This possibility is confirmed by experimental data on the crystallization of glasses with REEs and actinides (Pu, Am). The prospect for the disposal of glasses with the REE–MA fraction in deep boreholes is briefly considered.
{"title":"Thermal Effects and Glass Crystallization in Composite Matrices for Immobilization of the Rare-Earth Element–Minor Actinide Fraction of High-Level Radioactive Waste","authors":"Sergey V. Yudintsev, Michael I. Ojovan, V. Malkovsky","doi":"10.3390/jcs8020070","DOIUrl":"https://doi.org/10.3390/jcs8020070","url":null,"abstract":"The current policy of managing high-level waste (HLW) derived in the closed nuclear fuel cycle consists in their vitrification into B-Si or Al-P vitreous forms. These compounds have rather limited capacity with respect to the HLW (5–20 wt%), and their properties change over time due to devitrification of the glasses. Cardinal improvement in the management of HLW can be achieved by their separation onto groups of elements with similar properties, followed by their immobilization in robust waste forms (matrices) and emplacement in deep disposal facilities. One of the possible fractions contains trivalent rare-earth elements (REEs) and minor actinides (MAs = Am and Cm). REEs are the fission products of actinides, which are mainly represented by stable isotopes of elements from La to Gd as well as Y. This group also contains small amounts of short-lived radionuclides with half-lives (T1/2) from 284 days (144Ce) to 90 years (151Sm), including 147Pm (T1/2 = 2.6 years), 154Eu (T1/2 = 8.8 years), and 155Eu (T1/2 = 5 years). However, the main long-term environmental hazard of the REE–MA fraction is associated with Am and Cm, with half-lives from 18 years (244Cm) to 8500 years (245Cm), and their daughter products: 237Np (T1/2 = 2.14 × 106 years), 239Pu (T1/2 = 2.41 × 104 years), 240Pu (T1/2 = 6537 years), and 242Pu (T1/2 = 3.76 × 105 years), which should be immobilized into a durable waste form that prevents their release into the environment. Due to the heat generated by decaying radionuclides, the temperature of matrices with an REE–MA fraction will be increased by hundreds of centigrade above ambient. This process can be utilized by selecting a vitreous waste form that will crystallize to form durable crystalline phases with long-lived radionuclides. We estimated the thermal effects in a potential REE–MA glass composite material based on the size of the block, the content of waste, the time of storage before immobilization and after disposal, and showed that it is possible to select the waste loading, size of blocks, and storage time so that the temperature of the matrix during the first decades will reach 500–700 °C, which corresponds to the optimal range of glass crystallization. As a result, a glass–ceramic composite will be produced that contains monazite ((REE,MA)PO4) in phosphate glasses; britholite (Cax(REE,MA)10-x(SiO4)6O2) or zirconolite ((Ca,REE,MA)(Zr,REE,MA)(Ti,Al,Fe)2O7), in silicate systems. This possibility is confirmed by experimental data on the crystallization of glasses with REEs and actinides (Pu, Am). The prospect for the disposal of glasses with the REE–MA fraction in deep boreholes is briefly considered.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":" 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139786845","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}
Ruiqi Zheng, Jianyong Pang, Jian Sun, Yongqiang Su, Guoping Xu
In order to enhance the practical application of carbon-fiber-reinforced concrete (CFRC) in engineering, it is necessary to study the damage mechanism of CFRC. Experimental research on the mechanical properties of CFRC under multiple strain rates was conducted. Five different fiber contents were analyzed to study the compressive strength and tensile strength of CFRC, and the damage characteristics of CFRC under multiple strain rates were analyzed based on failure modes and energy changes. An energy-based damage constitutive model was established. The results showed the following: (1) When the carbon fiber content was 0.4%, CFRC had the best comprehensive performance, with a 15.02% increase in compressive strength and a 51.12% increase in tensile strength. With the increase in strain rate, the compressive strength of the concrete increased. (2) Under high strain rates, carbon fiber significantly enhanced the compressive strength of the concrete, and the input energy, elastic strain energy, and dissipated energy increased. The peak value of the elastic strain energy conversion rate increased, and the minimum value of the dissipated energy conversion rate decreased. (3) Under the same strain rate, the CFRC had a larger inflection point of dissipated energy corresponding to the strain compared to the reference group of concrete during the loading process. A constitutive model for CFRC was established based on damage mechanics and probability statistics. The research results will provide theoretical references for the application of carbon-fiber-reinforced concrete.
{"title":"Damage Model of Carbon-Fiber-Reinforced Concrete Based on Energy Conversion Principle","authors":"Ruiqi Zheng, Jianyong Pang, Jian Sun, Yongqiang Su, Guoping Xu","doi":"10.3390/jcs8020071","DOIUrl":"https://doi.org/10.3390/jcs8020071","url":null,"abstract":"In order to enhance the practical application of carbon-fiber-reinforced concrete (CFRC) in engineering, it is necessary to study the damage mechanism of CFRC. Experimental research on the mechanical properties of CFRC under multiple strain rates was conducted. Five different fiber contents were analyzed to study the compressive strength and tensile strength of CFRC, and the damage characteristics of CFRC under multiple strain rates were analyzed based on failure modes and energy changes. An energy-based damage constitutive model was established. The results showed the following: (1) When the carbon fiber content was 0.4%, CFRC had the best comprehensive performance, with a 15.02% increase in compressive strength and a 51.12% increase in tensile strength. With the increase in strain rate, the compressive strength of the concrete increased. (2) Under high strain rates, carbon fiber significantly enhanced the compressive strength of the concrete, and the input energy, elastic strain energy, and dissipated energy increased. The peak value of the elastic strain energy conversion rate increased, and the minimum value of the dissipated energy conversion rate decreased. (3) Under the same strain rate, the CFRC had a larger inflection point of dissipated energy corresponding to the strain compared to the reference group of concrete during the loading process. A constitutive model for CFRC was established based on damage mechanics and probability statistics. The research results will provide theoretical references for the application of carbon-fiber-reinforced concrete.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":" April","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139787347","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}
Sergey V. Yudintsev, Michael I. Ojovan, V. Malkovsky
The current policy of managing high-level waste (HLW) derived in the closed nuclear fuel cycle consists in their vitrification into B-Si or Al-P vitreous forms. These compounds have rather limited capacity with respect to the HLW (5–20 wt%), and their properties change over time due to devitrification of the glasses. Cardinal improvement in the management of HLW can be achieved by their separation onto groups of elements with similar properties, followed by their immobilization in robust waste forms (matrices) and emplacement in deep disposal facilities. One of the possible fractions contains trivalent rare-earth elements (REEs) and minor actinides (MAs = Am and Cm). REEs are the fission products of actinides, which are mainly represented by stable isotopes of elements from La to Gd as well as Y. This group also contains small amounts of short-lived radionuclides with half-lives (T1/2) from 284 days (144Ce) to 90 years (151Sm), including 147Pm (T1/2 = 2.6 years), 154Eu (T1/2 = 8.8 years), and 155Eu (T1/2 = 5 years). However, the main long-term environmental hazard of the REE–MA fraction is associated with Am and Cm, with half-lives from 18 years (244Cm) to 8500 years (245Cm), and their daughter products: 237Np (T1/2 = 2.14 × 106 years), 239Pu (T1/2 = 2.41 × 104 years), 240Pu (T1/2 = 6537 years), and 242Pu (T1/2 = 3.76 × 105 years), which should be immobilized into a durable waste form that prevents their release into the environment. Due to the heat generated by decaying radionuclides, the temperature of matrices with an REE–MA fraction will be increased by hundreds of centigrade above ambient. This process can be utilized by selecting a vitreous waste form that will crystallize to form durable crystalline phases with long-lived radionuclides. We estimated the thermal effects in a potential REE–MA glass composite material based on the size of the block, the content of waste, the time of storage before immobilization and after disposal, and showed that it is possible to select the waste loading, size of blocks, and storage time so that the temperature of the matrix during the first decades will reach 500–700 °C, which corresponds to the optimal range of glass crystallization. As a result, a glass–ceramic composite will be produced that contains monazite ((REE,MA)PO4) in phosphate glasses; britholite (Cax(REE,MA)10-x(SiO4)6O2) or zirconolite ((Ca,REE,MA)(Zr,REE,MA)(Ti,Al,Fe)2O7), in silicate systems. This possibility is confirmed by experimental data on the crystallization of glasses with REEs and actinides (Pu, Am). The prospect for the disposal of glasses with the REE–MA fraction in deep boreholes is briefly considered.
{"title":"Thermal Effects and Glass Crystallization in Composite Matrices for Immobilization of the Rare-Earth Element–Minor Actinide Fraction of High-Level Radioactive Waste","authors":"Sergey V. Yudintsev, Michael I. Ojovan, V. Malkovsky","doi":"10.3390/jcs8020070","DOIUrl":"https://doi.org/10.3390/jcs8020070","url":null,"abstract":"The current policy of managing high-level waste (HLW) derived in the closed nuclear fuel cycle consists in their vitrification into B-Si or Al-P vitreous forms. These compounds have rather limited capacity with respect to the HLW (5–20 wt%), and their properties change over time due to devitrification of the glasses. Cardinal improvement in the management of HLW can be achieved by their separation onto groups of elements with similar properties, followed by their immobilization in robust waste forms (matrices) and emplacement in deep disposal facilities. One of the possible fractions contains trivalent rare-earth elements (REEs) and minor actinides (MAs = Am and Cm). REEs are the fission products of actinides, which are mainly represented by stable isotopes of elements from La to Gd as well as Y. This group also contains small amounts of short-lived radionuclides with half-lives (T1/2) from 284 days (144Ce) to 90 years (151Sm), including 147Pm (T1/2 = 2.6 years), 154Eu (T1/2 = 8.8 years), and 155Eu (T1/2 = 5 years). However, the main long-term environmental hazard of the REE–MA fraction is associated with Am and Cm, with half-lives from 18 years (244Cm) to 8500 years (245Cm), and their daughter products: 237Np (T1/2 = 2.14 × 106 years), 239Pu (T1/2 = 2.41 × 104 years), 240Pu (T1/2 = 6537 years), and 242Pu (T1/2 = 3.76 × 105 years), which should be immobilized into a durable waste form that prevents their release into the environment. Due to the heat generated by decaying radionuclides, the temperature of matrices with an REE–MA fraction will be increased by hundreds of centigrade above ambient. This process can be utilized by selecting a vitreous waste form that will crystallize to form durable crystalline phases with long-lived radionuclides. We estimated the thermal effects in a potential REE–MA glass composite material based on the size of the block, the content of waste, the time of storage before immobilization and after disposal, and showed that it is possible to select the waste loading, size of blocks, and storage time so that the temperature of the matrix during the first decades will reach 500–700 °C, which corresponds to the optimal range of glass crystallization. As a result, a glass–ceramic composite will be produced that contains monazite ((REE,MA)PO4) in phosphate glasses; britholite (Cax(REE,MA)10-x(SiO4)6O2) or zirconolite ((Ca,REE,MA)(Zr,REE,MA)(Ti,Al,Fe)2O7), in silicate systems. This possibility is confirmed by experimental data on the crystallization of glasses with REEs and actinides (Pu, Am). The prospect for the disposal of glasses with the REE–MA fraction in deep boreholes is briefly considered.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"23 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139846679","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}
Ruiqi Zheng, Jianyong Pang, Jian Sun, Yongqiang Su, Guoping Xu
In order to enhance the practical application of carbon-fiber-reinforced concrete (CFRC) in engineering, it is necessary to study the damage mechanism of CFRC. Experimental research on the mechanical properties of CFRC under multiple strain rates was conducted. Five different fiber contents were analyzed to study the compressive strength and tensile strength of CFRC, and the damage characteristics of CFRC under multiple strain rates were analyzed based on failure modes and energy changes. An energy-based damage constitutive model was established. The results showed the following: (1) When the carbon fiber content was 0.4%, CFRC had the best comprehensive performance, with a 15.02% increase in compressive strength and a 51.12% increase in tensile strength. With the increase in strain rate, the compressive strength of the concrete increased. (2) Under high strain rates, carbon fiber significantly enhanced the compressive strength of the concrete, and the input energy, elastic strain energy, and dissipated energy increased. The peak value of the elastic strain energy conversion rate increased, and the minimum value of the dissipated energy conversion rate decreased. (3) Under the same strain rate, the CFRC had a larger inflection point of dissipated energy corresponding to the strain compared to the reference group of concrete during the loading process. A constitutive model for CFRC was established based on damage mechanics and probability statistics. The research results will provide theoretical references for the application of carbon-fiber-reinforced concrete.
{"title":"Damage Model of Carbon-Fiber-Reinforced Concrete Based on Energy Conversion Principle","authors":"Ruiqi Zheng, Jianyong Pang, Jian Sun, Yongqiang Su, Guoping Xu","doi":"10.3390/jcs8020071","DOIUrl":"https://doi.org/10.3390/jcs8020071","url":null,"abstract":"In order to enhance the practical application of carbon-fiber-reinforced concrete (CFRC) in engineering, it is necessary to study the damage mechanism of CFRC. Experimental research on the mechanical properties of CFRC under multiple strain rates was conducted. Five different fiber contents were analyzed to study the compressive strength and tensile strength of CFRC, and the damage characteristics of CFRC under multiple strain rates were analyzed based on failure modes and energy changes. An energy-based damage constitutive model was established. The results showed the following: (1) When the carbon fiber content was 0.4%, CFRC had the best comprehensive performance, with a 15.02% increase in compressive strength and a 51.12% increase in tensile strength. With the increase in strain rate, the compressive strength of the concrete increased. (2) Under high strain rates, carbon fiber significantly enhanced the compressive strength of the concrete, and the input energy, elastic strain energy, and dissipated energy increased. The peak value of the elastic strain energy conversion rate increased, and the minimum value of the dissipated energy conversion rate decreased. (3) Under the same strain rate, the CFRC had a larger inflection point of dissipated energy corresponding to the strain compared to the reference group of concrete during the loading process. A constitutive model for CFRC was established based on damage mechanics and probability statistics. The research results will provide theoretical references for the application of carbon-fiber-reinforced concrete.","PeriodicalId":502935,"journal":{"name":"Journal of Composites Science","volume":"230 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139847482","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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