Статті в журналах з теми "Green Chemistry Separation"
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Rogers, Luke, and Klavs F. Jensen. "Continuous manufacturing – the Green Chemistry promise?" Green Chemistry 21, no. 13 (2019): 3481–98. http://dx.doi.org/10.1039/c9gc00773c.
Повний текст джерелаClark, James H. "Catalysis for green chemistry." Pure and Applied Chemistry 73, no. 1 (January 1, 2001): 103–11. http://dx.doi.org/10.1351/pac200173010103.
Повний текст джерелаSahoo, Tejaswini, Jagannath Panda, Jnanaranjan Sahu, Dayananda Sarangi, Sunil K. Sahoo, Braja B. Nanda, and Rojalin Sahu. "Green Solvent: Green Shadow on Chemical Synthesis." Current Organic Synthesis 17, no. 6 (September 25, 2020): 426–39. http://dx.doi.org/10.2174/1570179417666200506102535.
Повний текст джерелаNamieśnik, Jacek. "Green analytical chemistry - Some remarks." Journal of Separation Science 24, no. 2 (February 1, 2001): 151–53. http://dx.doi.org/10.1002/1615-9314(20010201)24:2<151::aid-jssc151>3.0.co;2-4.
Повний текст джерелаDembek, Mikołaj, and Szymon Bocian. "Stationary Phases for Green Liquid Chromatography." Materials 15, no. 2 (January 6, 2022): 419. http://dx.doi.org/10.3390/ma15020419.
Повний текст джерелаSagandykova, Gulyaim, Michał Szumski, and Bogusław Buszewski. "How much separation sciences fit in the green chemistry canoe?" Current Opinion in Green and Sustainable Chemistry 30 (August 2021): 100495. http://dx.doi.org/10.1016/j.cogsc.2021.100495.
Повний текст джерелаDonato, Laura, Imen Iben Nasser, Mustapha Majdoub, and Enrico Drioli. "Green Chemistry and Molecularly Imprinted Membranes." Membranes 12, no. 5 (April 27, 2022): 472. http://dx.doi.org/10.3390/membranes12050472.
Повний текст джерелаZhang, Pengrui, Mingyong Wang, Jinhe Sun, Fei Shao, Yongzhong Jia, and Yan Jing. "Lithium Isotope Green Separation Using Water Scrubbing." Chemistry Letters 48, no. 12 (December 5, 2019): 1541–43. http://dx.doi.org/10.1246/cl.190669.
Повний текст джерелаKoel, Mihkel, and Mihkel Kaljurand. "Application of the principles of green chemistry in analytical chemistry." Pure and Applied Chemistry 78, no. 11 (January 1, 2006): 1993–2002. http://dx.doi.org/10.1351/pac200678111993.
Повний текст джерелаRichter, Steffi. "Green Separation Processes - Fundamentals and Applications." Environmental Science and Pollution Research - International 13, no. 2 (March 2006): 145. http://dx.doi.org/10.1065/espr2006.02.005.
Повний текст джерелаLee, Wei Jie, Pei Sean Goh, Woei Jye Lau, Ahmad Fauzi Ismail, and Nidal Hilal. "Green Approaches for Sustainable Development of Liquid Separation Membrane." Membranes 11, no. 4 (March 25, 2021): 235. http://dx.doi.org/10.3390/membranes11040235.
Повний текст джерелаBai, Fang, Jing Li, and Chao Hua. "Research Progresses of Deep Eutectic Solvents and its Application in Separation and Catalysis." Materials Science Forum 921 (May 2018): 3–12. http://dx.doi.org/10.4028/www.scientific.net/msf.921.3.
Повний текст джерелаNaccarato, Attilio. "Development and Application of Green or Sustainable Strategies in Analytical Chemistry." Separations 10, no. 1 (January 5, 2023): 32. http://dx.doi.org/10.3390/separations10010032.
Повний текст джерелаDogan, Aysegul, and Marek Tobiszewski. "Optimization of liquid chromatographic separation of pharmaceuticals within green analytical chemistry framework." Microchemical Journal 152 (January 2020): 104323. http://dx.doi.org/10.1016/j.microc.2019.104323.
Повний текст джерелаNie, Lirong, Chaochao Cai, Runpeng Guo, Shun Yao, Zhi Zhu, Yanchen Hong, and Dong Guo. "Ionic Liquid-Assisted DLLME and SPME for the Determination of Contaminants in Food Samples." Separations 9, no. 7 (July 6, 2022): 170. http://dx.doi.org/10.3390/separations9070170.
Повний текст джерелаHOU, Yucui, Congfei YAO, and Weize WU. "Deep Eutectic Solvents: Green Solvents for Separation Applications." Acta Physico-Chimica Sinica 34, no. 8 (2018): 873–85. http://dx.doi.org/10.3866/pku.whxb201802062.
Повний текст джерелаRen, Liwei, Tian Xu, Ruoping He, Zhenhua Jiang, Hua Zhou, and Ping Wei. "A green resolution–separation process for aliphatic secondary alcohols." Tetrahedron: Asymmetry 24, no. 5-6 (March 2013): 249–53. http://dx.doi.org/10.1016/j.tetasy.2013.01.018.
Повний текст джерелаVono, Lucas L. R., Camila C. Damasceno, Jivaldo R. Matos, Renato F. Jardim, Richard Landers, Sueli H. Masunaga, and Liane M. Rossi. "Separation technology meets green chemistry: development of magnetically recoverable catalyst supports containing silica, ceria, and titania." Pure and Applied Chemistry 90, no. 1 (January 26, 2018): 133–41. http://dx.doi.org/10.1515/pac-2017-0504.
Повний текст джерелаBandara, H. M. Dhammika, Kathleen D. Field, and Marion H. Emmert. "Rare earth recovery from end-of-life motors employing green chemistry design principles." Green Chemistry 18, no. 3 (2016): 753–59. http://dx.doi.org/10.1039/c5gc01255d.
Повний текст джерелаHung, M. T., and J. C. Liu. "Microfiltration for separation of green algae from water." Colloids and Surfaces B: Biointerfaces 51, no. 2 (August 2006): 157–64. http://dx.doi.org/10.1016/j.colsurfb.2006.07.003.
Повний текст джерелаHao, Jianxiu, Limin Han, Keli Yang, Hongye Zhao, Xiaomin Li, Yanpeng Ban, Na Li, Huacong Zhou, and Quansheng Liu. "Metal ion-induced separation of valuable organic acids from a depolymerized mixture of lignite without using organic solvents." RSC Advances 10, no. 6 (2020): 3479–86. http://dx.doi.org/10.1039/c9ra10542e.
Повний текст джерелаGhanbari Kermanshahi, Mohammad, and Kiumars Bahrami. "Fe3O4@BNPs@SiO2–SO3H as a highly chemoselective heterogeneous magnetic nanocatalyst for the oxidation of sulfides to sulfoxides or sulfones." RSC Advances 9, no. 62 (2019): 36103–12. http://dx.doi.org/10.1039/c9ra06221a.
Повний текст джерелаZverev, I. V., A. V. Podgaetskii, and S. A. Fadeev. "Separation of kerogen from green river oil shale." Solid Fuel Chemistry 50, no. 4 (July 2016): 248–55. http://dx.doi.org/10.3103/s0361521916040121.
Повний текст джерелаLiu, Wenbo, and Chao-Jun Li. "Recent Synthetic Applications of Catalyst-Free Photochemistry." Synlett 28, no. 20 (September 14, 2017): 2714–54. http://dx.doi.org/10.1055/s-0036-1590900.
Повний текст джерелаAbdel Hameed, Eman A., Zaitona A. Abd El-Naby, Alaa El Gindy, Sawsan A. Zaitone, Reem Alshaman, Roshdy E. Saraya, and Gasser M. Khairy. "Two New HPLC Methods, Assessed by GAPI, for Simultaneous Determination of Four Antipsychotics in Pharmaceutical Formulations: A Comparative Study." Separations 9, no. 8 (August 15, 2022): 220. http://dx.doi.org/10.3390/separations9080220.
Повний текст джерелаFrancioso, Antonio, Silvestro Dupré, and Mario Fontana. "Chemistry of Outlandish Natural Products Belonging to Sulfur Metabolism: Unrevealed Green Syntheses and Separation Strategies from the Cavallini’s Old School." Separations 9, no. 2 (February 7, 2022): 45. http://dx.doi.org/10.3390/separations9020045.
Повний текст джерелаKoina, Ioulia Maria, Yiannis Sarigiannis, and Evroula Hapeshi. "Green Extraction Techniques for the Determination of Active Ingredients in Tea: Current State, Challenges, and Future Perspectives." Separations 10, no. 2 (February 9, 2023): 121. http://dx.doi.org/10.3390/separations10020121.
Повний текст джерелаDas, Saikat, Jie Feng, and Wei Wang. "Covalent Organic Frameworks in Separation." Annual Review of Chemical and Biomolecular Engineering 11, no. 1 (June 7, 2020): 131–53. http://dx.doi.org/10.1146/annurev-chembioeng-112019-084830.
Повний текст джерелаRaza, Ayesha, Sarah Farrukh, Arshad Hussain, Imranullah Khan, Mohd Hafiz Dzarfan Othman, and Muhammad Ahsan. "Performance Analysis of Blended Membranes of Cellulose Acetate with Variable Degree of Acetylation for CO2/CH4 Separation." Membranes 11, no. 4 (March 29, 2021): 245. http://dx.doi.org/10.3390/membranes11040245.
Повний текст джерелаWang, Shuai, Xuan Li, and Jun Jie Zhang. "Rapid Photochemical Synthesis of 6-Methyl-1-Indanone." Advanced Materials Research 634-638 (January 2013): 416–19. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.416.
Повний текст джерелаAzimi, Sabikeh G., Ghodsieh Bagherzade, Mohammad Reza Saberi, and Zeinab Amiri Tehranizadeh. "Discovery of New Ligand with Quinoline Scaffold as Potent Allosteric Inhibitor of HIV-1 and Its Copper Complexes as a Powerful Catalyst for the Synthesis of Chiral Benzimidazole Derivatives, and in Silico Anti-HIV-1 Studies." Bioinorganic Chemistry and Applications 2023 (April 21, 2023): 1–17. http://dx.doi.org/10.1155/2023/2881582.
Повний текст джерелаFeder-Kubis, Joanna, Jolanta Flieger, Małgorzata Tatarczak-Michalewska, Anita Płazińska, Anna Madejska, and Marta Swatko-Ossor. "Renewable sources from plants as the starting material for designing new terpene chiral ionic liquids used for the chromatographic separation of acidic enantiomers." RSC Advances 7, no. 51 (2017): 32344–56. http://dx.doi.org/10.1039/c7ra03310a.
Повний текст джерелаAl-Tannak, Naser F., and Ahmed Hemdan. "Eco-Friendly Separation of Antihyperlipidemic Combination Using UHPLC Particle-Packed and Monolithic Columns by Applying Green Analytical Chemistry Principles." Separations 8, no. 12 (December 14, 2021): 246. http://dx.doi.org/10.3390/separations8120246.
Повний текст джерелаYAYABE, Fumihisa, Hitoshi KINUGASA, and Tadakazu TAKEO. "A simple preparative chromatographic separation of green tea catechins." Journal of the agricultural chemical society of Japan 63, no. 4 (1989): 845–47. http://dx.doi.org/10.1271/nogeikagaku1924.63.845.
Повний текст джерелаKaur, Pawanpreet, and Harish Kumar Chopra. "Recent Advances in Applications of Supported Ionic Liquids." Current Organic Chemistry 23, no. 26 (January 1, 2020): 2881–915. http://dx.doi.org/10.2174/1385272823666191204151803.
Повний текст джерелаFu, Ye, and Zhiguang Guo. "Natural polysaccharide-based aerogels and their applications in oil–water separations: a review." Journal of Materials Chemistry A 10, no. 15 (2022): 8129–58. http://dx.doi.org/10.1039/d2ta00708h.
Повний текст джерелаBorpatra Gohain, Moucham, Sachin Karki, Diksha Yadav, Archana Yadav, Neha R. Thakare, Swapnali Hazarika, Hyung Keun Lee, and Pravin G. Ingole. "Development of Antifouling Thin-Film Composite/Nanocomposite Membranes for Removal of Phosphate and Malachite Green Dye." Membranes 12, no. 8 (August 7, 2022): 768. http://dx.doi.org/10.3390/membranes12080768.
Повний текст джерелаFeng, Xueting, Hang Song, Tenghe Zhang, Shun Yao, and Yan Wang. "Magnetic Technologies and Green Solvents in Extraction and Separation of Bioactive Molecules Together with Biochemical Objects: Current Opportunities and Challenges." Separations 9, no. 11 (November 3, 2022): 346. http://dx.doi.org/10.3390/separations9110346.
Повний текст джерелаMichalski, Rajmund, and Paulina Pecyna-Utylska. "Green Aspects of Ion Chromatography versus Other Methods in the Analysis of Common Inorganic Ions." Separations 8, no. 12 (December 3, 2021): 235. http://dx.doi.org/10.3390/separations8120235.
Повний текст джерелаRubiyanto, Dwiarso, Nurcahyo Iman Prakoso, Imam Sahroni, Rico Nurillahi, and Is Fatimah. "ZnO-Porous Clay Heterostructure from Saponite as Green Catalyst for Citronellal Cyclization." Bulletin of Chemical Reaction Engineering & Catalysis 15, no. 1 (November 13, 2019): 137–45. http://dx.doi.org/10.9767/bcrec.15.1.5800.137-145.
Повний текст джерелаMohammad, Ali, and Nazrul Haq. "TLC separation of amino acids with a green mobile phase." Journal of Planar Chromatography – Modern TLC 23, no. 4 (August 2010): 260–64. http://dx.doi.org/10.1556/jpc.23.2010.4.4.
Повний текст джерелаSamanidou, Victoria, and Abuzar Kabir. "Magnet Integrated Fabric Phase Sorptive Extraction (MI-FPSE): A Powerful Green(er) Alternative for Sample Preparation." Analytica 3, no. 4 (December 2, 2022): 439–47. http://dx.doi.org/10.3390/analytica3040030.
Повний текст джерелаGuo, Weiwei, Qi Zhang, Yang Cao, Kaihua Cai, Shengyong Zhang, and Yonghai Chai. "Environmentally benign access to isoindolinones: synthesis, separation and resource recycling." Green Chemistry 22, no. 9 (2020): 2873–78. http://dx.doi.org/10.1039/d0gc00957a.
Повний текст джерелаPradel, Jean Sebastien, and William G. Tong. "Determination of malachite green, crystal violet, brilliant green and methylene blue by micro-cloud-point extraction and nonlinear laser wave-mixing detection interfaced to micellar capillary electrophoresis." Analytical Methods 9, no. 45 (2017): 6411–19. http://dx.doi.org/10.1039/c7ay01706e.
Повний текст джерелаZhang, Chunhui, Yuheng Zhang, Xiao Xiao, Guoliang Liu, Zhe Xu, Bing Wang, Cunming Yu, Robin H. A. Ras, and Lei Jiang. "Correction: Efficient separation of immiscible oil/water mixtures using a perforated lotus leaf." Green Chemistry 22, no. 2 (2020): 565–66. http://dx.doi.org/10.1039/c9gc90121c.
Повний текст джерелаAsimi Neisiani, A., R. Saneie, A. Mohammadzadeh, D. G. Wonyen, and S. Chehreh Chelgani. "Biodegradable hematite depressants for green flotation separation – An overview." Minerals Engineering 199 (August 2023): 108114. http://dx.doi.org/10.1016/j.mineng.2023.108114.
Повний текст джерелаSantali, Eman Y., Ibrahim A. Naguib, Abdullah M. Alshehri, Yazeed A. Alzahrani, Abdullah E. Alharthi, Turki S. Alosaimi, Bandar D. Alsayali, et al. "Greenness Assessment of Chromatographic Methods Used for Analysis of Empagliflozin: A Comparative Study." Separations 9, no. 10 (October 1, 2022): 275. http://dx.doi.org/10.3390/separations9100275.
Повний текст джерелаChen, Guang-Hui, Yan-Ping He, Fu-Pei Liang, Lei Zhang, and Jian Zhang. "A green separation process of Ag via a Ti4(embonate)6 cage." Dalton Transactions 49, no. 47 (2020): 17194–99. http://dx.doi.org/10.1039/d0dt03214j.
Повний текст джерелаZeng, Shaojuan, Yongkang Cao, Pengfei Li, Xinyan Liu, and Xiangping Zhang. "Ionic liquid–based green processes for ammonia separation and recovery." Current Opinion in Green and Sustainable Chemistry 25 (October 2020): 100354. http://dx.doi.org/10.1016/j.cogsc.2020.100354.
Повний текст джерелаZhuang, Guo-Liang, Chao-Fong Wu, Ming-Yen Wey, and Hui-Hsin Tseng. "Impacts of Green Synthesis Process on Asymmetric Hybrid PDMS Membrane for Efficient CO2/N2 Separation." Membranes 11, no. 1 (January 15, 2021): 59. http://dx.doi.org/10.3390/membranes11010059.
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