Polymers Synthesis and Characterization
Polymer science represents a domain of great interest due to the possible applications of polymers in areas that range from the most common to those that are high-tech. To achieve this, synthesis and characterization techniques, as well as the correlation of the chemical structure and morphology wit...
Format: | eBook |
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Language: | English |
Published: |
Basel
MDPI - Multidisciplinary Digital Publishing Institute
2023
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Subjects: | |
Online Access: | Open Access: DOAB: description of the publication Open Access: DOAB, download the publication |
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245 | 0 | 0 | |a Polymers Synthesis and Characterization |
260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2023 | ||
300 | |a 1 online resource (774 p.) | ||
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520 | |a Polymer science represents a domain of great interest due to the possible applications of polymers in areas that range from the most common to those that are high-tech. To achieve this, synthesis and characterization techniques, as well as the correlation of the chemical structure and morphology with their properties, is critical. From the perspective of synthesis, there are two strategies for obtaining polymers: step-growth (polyaddition, polycondensation, and reversible-deactivation radical polymerization) and chain polymerization (radical polymerization, coordinative polymerization, and cationic and anionic polymerization).The advancement of polymer applications continues to lead to the expansion of the synthesis and characterization techniques that can be facilitated by novel, smart, multifunctional polymers. There is a correlation between structure, composition, morphology, and properties of applications that leads to substantial benefits for specific applications.This Special Issue will establish a collection of articles and reviews that follow the latest developments in polymer synthesis, their characterization techniques, and the correlation between structure and properties. | ||
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546 | |a English | ||
650 | 7 | |a History of engineering & technology |2 bicssc | |
650 | 7 | |a Technology: general issues |2 bicssc | |
653 | |a "green" chelates | ||
653 | |a 1-olefin | ||
653 | |a 1,3-butadiene | ||
653 | |a 3D dosimetry | ||
653 | |a absorbed dose | ||
653 | |a active coatings | ||
653 | |a adsorption | ||
653 | |a adsorption isotherms | ||
653 | |a adsorption kinetics | ||
653 | |a agro-industrial waste | ||
653 | |a alginate | ||
653 | |a and excitonic state | ||
653 | |a anti-solvent precipitation | ||
653 | |a antimicrobial activity | ||
653 | |a antimicrobial materials | ||
653 | |a antioxidant | ||
653 | |a apigenin | ||
653 | |a application | ||
653 | |a atomic force microscopy | ||
653 | |a ATRP | ||
653 | |a aza-Michael addition | ||
653 | |a ballistic protection | ||
653 | |a benzoxazines cure | ||
653 | |a beta-cyclodextrin | ||
653 | |a bimetallic | ||
653 | |a binder | ||
653 | |a bioavailability | ||
653 | |a biodegradability | ||
653 | |a biodegradable polyesters | ||
653 | |a biological agents | ||
653 | |a bisphenol A adsorption | ||
653 | |a bisphenol F | ||
653 | |a Box-Behnken design | ||
653 | |a bromination | ||
653 | |a bubble column reactor | ||
653 | |a catalysis | ||
653 | |a characterization | ||
653 | |a chemical warfare agents | ||
653 | |a chitosan | ||
653 | |a chloroform | ||
653 | |a ciprofloxacin (CIP) | ||
653 | |a cis-1,4 selective | ||
653 | |a coatings | ||
653 | |a color | ||
653 | |a comb-like polymer | ||
653 | |a complexing agents | ||
653 | |a composite | ||
653 | |a conversion | ||
653 | |a cooperated | ||
653 | |a coordination polymer | ||
653 | |a copolymerization | ||
653 | |a copolymers | ||
653 | |a crystal structure analysis | ||
653 | |a CuAAC | ||
653 | |a curing agent | ||
653 | |a cyanide polymerization | ||
653 | |a damping property | ||
653 | |a decontamination | ||
653 | |a Diels-Alder reaction | ||
653 | |a dimethyl carbonate | ||
653 | |a dimethyl methylphosphonate (DMMP) | ||
653 | |a direct arylation polycondensation | ||
653 | |a disperse dyes | ||
653 | |a distribution | ||
653 | |a dosimetric properties | ||
653 | |a eco-friendly | ||
653 | |a elastomer | ||
653 | |a emulsion polymerization | ||
653 | |a end group effect | ||
653 | |a entanglement | ||
653 | |a environmental concern | ||
653 | |a epoxy oligomer | ||
653 | |a epoxy resin | ||
653 | |a epoxyurethane oligomer | ||
653 | |a equilibrium transesterification level | ||
653 | |a ethylene | ||
653 | |a extraction | ||
653 | |a flame retardant | ||
653 | |a fluorescence | ||
653 | |a free radical polymerization | ||
653 | |a Gabriel reaction | ||
653 | |a GC-MS/MS spectrometry | ||
653 | |a gelatin | ||
653 | |a glass transition temperature | ||
653 | |a glycidyl methacrylate | ||
653 | |a HCN polymers | ||
653 | |a heavy metal | ||
653 | |a high molecular weight | ||
653 | |a Hopkinson bar | ||
653 | |a host-guest strategy | ||
653 | |a hydrogel | ||
653 | |a hydrolysis resistance | ||
653 | |a hydrophobically associating water-soluble polymers | ||
653 | |a IA-PAE | ||
653 | |a in vitro drug dissolution | ||
653 | |a interpenetrating network | ||
653 | |a intramolecular charge transfer | ||
653 | |a IR spectrometry | ||
653 | |a kaolin | ||
653 | |a kinetic modeling | ||
653 | |a levofloxacin (LEV) | ||
653 | |a limestone | ||
653 | |a linear polyurethane | ||
653 | |a low-energy electron beam | ||
653 | |a lowest energetic consumption | ||
653 | |a luminescence | ||
653 | |a mechanical properties | ||
653 | |a melt polycondensation | ||
653 | |a microwave irradiation | ||
653 | |a microwave reactor | ||
653 | |a microwave-driven polymerization | ||
653 | |a miscibility | ||
653 | |a mixed microbial cultures | ||
653 | |a molecular brushes | ||
653 | |a multifunctional materials | ||
653 | |a multiwall carbon nanotubes (MWCNTs) | ||
653 | |a nanocomposite | ||
653 | |a nanocomposite films | ||
653 | |a nanofibers | ||
653 | |a nanoparticles | ||
653 | |a nanosuspension | ||
653 | |a natural resource | ||
653 | |a NIR laser irradiation | ||
653 | |a non-ionic waterborne polyester | ||
653 | |a olefin polymerization | ||
653 | |a oligopeptide length | ||
653 | |a oligotetramethylene oxide diol | ||
653 | |a one-pot method | ||
653 | |a organic catalyst | ||
653 | |a overall heat transfer coefficient | ||
653 | |a PC-PDMS copolymer | ||
653 | |a peeling | ||
653 | |a PET | ||
653 | |a PHB | ||
653 | |a phosphazene | ||
653 | |a phosphazenes | ||
653 | |a photothermal modeling | ||
653 | |a photothermal transduction efficiency | ||
653 | |a poly(methyl methacrylate) | ||
653 | |a poly(octadecyl acrylate) | ||
653 | |a poly(stearyl acrylate) | ||
653 | |a poly(vinylpyrrolidone) | ||
653 | |a poly(ε-caprolactone) | ||
653 | |a polyamide | ||
653 | |a polyester fabrics | ||
653 | |a polyethylene | ||
653 | |a polyethylene terephthalate recycling | ||
653 | |a polyhydroxyalkanoates | ||
653 | |a polyimide | ||
653 | |a polyisoprene | ||
653 | |a polymer | ||
653 | |a polymer dosimeter | ||
653 | |a polymeric composite | ||
653 | |a polymeric emulsifier | ||
653 | |a polymerization | ||
653 | |a polymers | ||
653 | |a polypyrrole nanoparticles | ||
653 | |a polyurea-polyurethane | ||
653 | |a polyurethane | ||
653 | |a polyurethanes | ||
653 | |a polyvinyl chloride | ||
653 | |a post-metallocene catalyst | ||
653 | |a PPG diamine | ||
653 | |a radiation crosslinking | ||
653 | |a radiation therapy | ||
653 | |a radioactive material | ||
653 | |a radiofluorogenic | ||
653 | |a radionuclide | ||
653 | |a RAFT copolymerization | ||
653 | |a RAFT polymerization | ||
653 | |a reverse iodine transfer polymerization | ||
653 | |a rheological behaviors | ||
653 | |a rheology | ||
653 | |a rocket propellant | ||
653 | |a ROP | ||
653 | |a salt tolerance | ||
653 | |a sand | ||
653 | |a semi-crystalline polymer | ||
653 | |a sheets | ||
653 | |a side chain crystalline polymer | ||
653 | |a silica | ||
653 | |a sodium alginate | ||
653 | |a sodium hypochlorite | ||
653 | |a solubility | ||
653 | |a soybean oil fatty acids | ||
653 | |a starch | ||
653 | |a starch bio-composite | ||
653 | |a strippable coating | ||
653 | |a styrene | ||
653 | |a styrene-acrylic emulsion | ||
653 | |a styrenic monomer | ||
653 | |a subscale rocket motor | ||
653 | |a sulfur mustard (HD) | ||
653 | |a superabsorbent composites | ||
653 | |a surface decontamination | ||
653 | |a sustainability | ||
653 | |a swelling behavior | ||
653 | |a synthesis | ||
653 | |a synthetic | ||
653 | |a TBD | ||
653 | |a terminal block | ||
653 | |a thermal analysis | ||
653 | |a thermally self-healing | ||
653 | |a tissue-equivalent phantom | ||
653 | |a titanium dioxide | ||
653 | |a ultraviolet protection factor | ||
653 | |a X-Ray diffraction | ||
653 | |a xanthan gum | ||
653 | |a Ziegler-Natta | ||
653 | |a α-diimine cobalt complexes | ||
653 | |a α,ω-alkenol | ||
653 | |a β-cyclodextrin | ||
653 | |a π − π stacking | ||
653 | |a π-π stacking interactions | ||
793 | 0 | |a DOAB Library. | |
856 | 4 | 0 | |u https://directory.doabooks.org/handle/20.500.12854/100044 |7 0 |z Open Access: DOAB: description of the publication |
856 | 4 | 0 | |u https://mdpi.com/books/pdfview/book/7137 |7 0 |z Open Access: DOAB, download the publication |