Читать книгу The Chemistry of Environmental Engineering - Johannes Karl Fink - Страница 4

1 Chapter 1Figure 1.1 Ethylene-bis(tetrahydroindenyl) zirconium dichloride.Figure 1.2 Vinyl triethoxysilane.Figure 1.3 Young’s modulus versus CNT volume fraction (9).Figure 1.4 polymerization of amino-containing styrenic monomers (15).Figure 1.5 Terpenes.Figure 1.6 3-Tris(trimethylsiloxy)silylpropyl sulfonate.Figure 1.7 Surfactants.Figure 1.8 Cationic silicone surfactants.Figure 1.9 Synthesis silicone surfactant (37).Figure 1.10 Poly(oxyethylene trisiloxane).Figure 1.11 Variation of the surface tension with the concentration of sur...Figure 1.12 Si4-PEGn, Si4Ph3-PEGn, Si4Ph6-PEGn.Figure 1.13 Synthesis of BAAM copolymers (78).Figure 1.14 compounds for fluorine-containing nanocontainers.Figure 1.15 2-(3-(3-Imidazolylpropyl)ureido)ethyl acrylate.Figure 1.16 Spiropyran mechanophore (84).Figure 1.17 Histidine.Figure 1.18 Diols.Figure 1.19 Diisocyanate monomers.Figure 1.20 Polythiol crosslinking agents.Figure 1.21 2,2´-Dimethoxy-2-phenylacetophenone.Figure 1.22 Isosorbide.

2 Chapter 2Figure 2.1 1H,1H,2H,2H-Perfluorodecyltrichlorosilane.Figure 2.2 Antibiotics.Figure 2.3 Branched chain monomers.Figure 2.4 Crosslinking agents.Figure 2.5 Adsorption isotherms of colloids and activated carbon (30).Figure 2.6 Monomers for esterification reaction.Figure 2.7 N-Isopropylmethacrylamide.Figure 2.8 N-Methylaniline.Figure 2.9 Tobramycin.Figure 2.10 Aqueous monomers.Figure 2.11 2-(Methacryloyloxy)ethyl dimethyl-(3-sulfopropyl) ammonium hyd...

3 Chapter 3Figure 3.1 Components for vinyl macromonomers.Figure 3.2 Polymethine compounds.Figure 3.3 Dithioesters.Figure 3.4 Xanthates.Figure 3.5 Synthesis of 4-cyano-4-[(thiobenzoyl)sulfanyl]pentanoic acid (4...Figure 3.6 Monomers for RAFT polymerization.Figure 3.7 Laccase.Figure 3.8 Nisin.Figure 3.9 Contact Angle Versus Soaking Time (101).

4 Chapter 4Figure 4.1 Recovered products.Figure 4.2 Products from chemical recycling of PET.

5 Chapter 5Figure 5.1 Atenolol.Figure 5.2 Acetaminophen.Figure 5.3 Methyl violet.Figure 5.4 Colors.

6 Chapter 6Figure 6.1 Avermectin B1a.Figure 6.2 Atrazine.Figure 6.3 Methyl paraoxon.Figure 6.4 Hydrolysis kinetics of methyl paraoxon (3).Figure 6.5 2,4-Dichlorophenoxyacetic acid.Figure 6.6 Thiram.Figure 6.7 Pesticides.Figure 6.8 Agrochemicals.Figure 6.9 Dichlorvos.Figure 6.10 Brilliant cresyl blue.Figure 6.11 Materials for an amperometric carbaryl biosensor.Figure 6.12 Compounds for Electrochemical Sensing.Figure 6.13 Phoxim .Figure 6.14 Compounds for molecularly imprinted sensor.Figure 6.15 Thiamethoxam.

7 Chapter 7Figure 7.1 1H,1H,2H,2H-perfluorooctyl trimethoxysilane.Figure 7.2 Poly(9,9-dioctylfluorene-alt-benzothiadiazole).Figure 7.3 poly [9,9-dioctyl fluorene-9,9-(bis(3,(N,N-dimethylamino)-N-eth...Figure 7.4 Bromophenylethynyl trimethylsilane.Figure 7.5 Bis(4-methoxyphenyl) maleimide.Figure 7.6 Tris(1-phenylisoquinoline)iridium(III).Figure 7.7 PF-CzBTO structure.Figure 7.8 Monomers for PEDOT and PSS.Figure 7.9 N-([1,1’-Biphenyl]-4-yl)-N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9’-...Figure 7.10 Acridine monomers.Figure 7.11 1-(4-Bromophenyl)-2-phenylbenzimidazole.Figure 7.12 Thiophene and triazole derivatives.Figure 7.13 Meldrum’s acid, 2,2-dimethyl-1,3-dioxane-4,6-dione.

8 Chapter 8Figure 8.1 Activating reagents.Figure 8.2 Histamine.

9 Chapter 9Figure 9.1 1,2-Dioleoyloxy-3-trimethylammonium propane.Figure 9.2 Cholesterol.Figure 9.3 Hyaluronic acid.Figure 9.4 Synthesis of a biodegradable conducting monomer (13).Figure 9.5 2-(Trichloroacetyl)pyrrole.Figure 9.6 Isobornyl acrylate.Figure 9.7 Uptake at room temperature in weight percent of PLA (41).