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Book
Intramolecular Hydrogen Bonding 2021
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Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

This book describes the results of both theoretical and experimental research on many topical issues in intramolecular hydrogen bonding. Its great advantage is that the presented research results have been obtained using many different techniques. Therefore, it is an excellent review of these methods, while showing their applicability to the current scientific issues regarding intramolecular hydrogen bonds. The experimental techniques used include X-ray diffraction, infrared and Raman spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), nuclear quadrupole resonance spectroscopy (NQR), incoherent inelastic neutron scattering (IINS), and differential scanning calorimetry (DSC). The solvatochromic and luminescent studies are also described. On the other hand, theoretical research is based on ab initio calculations and the Car–Parrinello Molecular Dynamics (CPMD). In the latter case, a description of nuclear quantum effects (NQE) is also possible. This book also demonstrates the use of theoretical methods such as Quantum Theory of Atoms in Molecules (QTAIM), Interacting Quantum Atoms (IQA), Natural Bond Orbital (NBO), Non-Covalent Interactions (NCI) index, Molecular Tailoring Approach (MTA), and many others.

Keywords

Research & information: general --- intramolecular interaction --- interaction energy --- hydrogen bond --- intramolecular hydrogen bonds --- deuterium isotope effects on chemical shifts --- isotope ratios --- hydrogen bond energies --- intramolecular hydrogen bonding --- high-accuracy extrapolation methods --- QTAIM --- non-covalent interactions --- local vibrational modes --- hydrogen bond (HB) --- intramolecular hydrogen bond (IHB) --- molecular tailoring approach (MTA) --- fragmentation methods --- bond energy estimation --- noncovalent interactions --- structures and binding energies --- charge-transfer interactions --- spin–spin coupling constants --- polymorphism --- isomerization --- phase transition --- nitro group --- matrix isolation --- IINS --- FT-IR --- Raman --- X-ray --- NQR --- DSC --- DFT --- Schiff base --- N-salicylidene aniline derivative --- photophysical properties --- solvatochromism --- Hirshfeld surface analysis --- amino-alcohols --- α-substitution --- beryllium bonds --- calculated infrared spectra --- interacting quantum atoms --- resonance-assisted hydrogen bond --- Schiff bases --- inelastic incoherent neutron scattering --- isotopic effect --- excited-state intramolecular proton transfer --- photochemistry --- photobiology --- quantum chemistry --- molecular dynamics --- ultrafast processes --- gas phase --- crystalline phase --- MP2 --- CCSD --- AIM --- SAPT --- nuclear quantum effects --- CPMD --- n/a --- spin-spin coupling constants


Book
Intramolecular Hydrogen Bonding 2021
Author:
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

This book describes the results of both theoretical and experimental research on many topical issues in intramolecular hydrogen bonding. Its great advantage is that the presented research results have been obtained using many different techniques. Therefore, it is an excellent review of these methods, while showing their applicability to the current scientific issues regarding intramolecular hydrogen bonds. The experimental techniques used include X-ray diffraction, infrared and Raman spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), nuclear quadrupole resonance spectroscopy (NQR), incoherent inelastic neutron scattering (IINS), and differential scanning calorimetry (DSC). The solvatochromic and luminescent studies are also described. On the other hand, theoretical research is based on ab initio calculations and the Car–Parrinello Molecular Dynamics (CPMD). In the latter case, a description of nuclear quantum effects (NQE) is also possible. This book also demonstrates the use of theoretical methods such as Quantum Theory of Atoms in Molecules (QTAIM), Interacting Quantum Atoms (IQA), Natural Bond Orbital (NBO), Non-Covalent Interactions (NCI) index, Molecular Tailoring Approach (MTA), and many others.


Book
Insecticide, Acaricide, Repellent and Antimicrobial Development
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

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Abstract

The present book, a reprint of the Molecules Special Issue "Insecticide, Acaricide, Repellent and Antimicrobial Development", presents key advances in the development of effective and eco-friendly insecticides, acaricides, repellents, and antimicrobials, including products of natural origin.

Keywords

Medicine --- Lauraceae --- Aedes aegypti --- Aedes albopictus --- Culex quinquefasciatus --- antibacterial --- antifungal --- antioxidants --- compatibility --- date palm dust mites --- host defense --- Oligonychus afrasiaticus --- Metarhizium anisopliae --- natural acaricide --- synergism --- 1-Chlorooctadecane --- Lamiaceae --- Clinopodium nepeta subsp. nepeta --- Clinopodium nepeta subsp. glandulosum --- essential oils --- chemical variability --- biological activities --- Citrullus colocynthis --- spinasterol, 22,23-dihydrospinasterol --- fernenol --- insecticidal activity --- LC50 --- electrical penetration graph --- peach potato aphid --- antifeedants --- attractants --- structure-activity relationships --- fractionation --- reducing activity --- biomolecules --- antibiofilm --- microbial infection --- mangrove --- larvicidal activity --- enzyme inhibition --- Rhizophora mucronata --- repellent --- mosquitoes --- Erigeron --- Conyza bonariensis --- Conyza canadensis --- Conyza sumatrensis --- mosquito --- vector control --- naphthoquinones --- plumbagin --- Spodoptera littoralis --- insect growth inhibition --- carnivorous plants --- Nepenthes --- botanical-based insecticide --- cereals --- green grain protectant --- essential oil nanoformulation --- stored-product beetles --- Tenebrionidae --- Chagas' disease transmission --- triatomines --- peridomiciliary use --- Argentina --- biopesticides --- bio-based pesticides --- chemical ecology --- pest control --- natural products --- storage --- monoterpenes --- bioinsecticide --- insect pest --- toxicity --- eugenol derivatives --- amino alcohols --- semisynthetic insecticides --- bioinsecticides --- phenylpropanoids --- Spodoptera frugiperda --- urban pests --- agricultural pests --- aphids --- cockroaches --- kissing bugs --- insect vectors --- green insecticides --- moth pests --- non-target toxicity --- stored product pests --- termites --- Lauraceae --- Aedes aegypti --- Aedes albopictus --- Culex quinquefasciatus --- antibacterial --- antifungal --- antioxidants --- compatibility --- date palm dust mites --- host defense --- Oligonychus afrasiaticus --- Metarhizium anisopliae --- natural acaricide --- synergism --- 1-Chlorooctadecane --- Lamiaceae --- Clinopodium nepeta subsp. nepeta --- Clinopodium nepeta subsp. glandulosum --- essential oils --- chemical variability --- biological activities --- Citrullus colocynthis --- spinasterol, 22,23-dihydrospinasterol --- fernenol --- insecticidal activity --- LC50 --- electrical penetration graph --- peach potato aphid --- antifeedants --- attractants --- structure-activity relationships --- fractionation --- reducing activity --- biomolecules --- antibiofilm --- microbial infection --- mangrove --- larvicidal activity --- enzyme inhibition --- Rhizophora mucronata --- repellent --- mosquitoes --- Erigeron --- Conyza bonariensis --- Conyza canadensis --- Conyza sumatrensis --- mosquito --- vector control --- naphthoquinones --- plumbagin --- Spodoptera littoralis --- insect growth inhibition --- carnivorous plants --- Nepenthes --- botanical-based insecticide --- cereals --- green grain protectant --- essential oil nanoformulation --- stored-product beetles --- Tenebrionidae --- Chagas' disease transmission --- triatomines --- peridomiciliary use --- Argentina --- biopesticides --- bio-based pesticides --- chemical ecology --- pest control --- natural products --- storage --- monoterpenes --- bioinsecticide --- insect pest --- toxicity --- eugenol derivatives --- amino alcohols --- semisynthetic insecticides --- bioinsecticides --- phenylpropanoids --- Spodoptera frugiperda --- urban pests --- agricultural pests --- aphids --- cockroaches --- kissing bugs --- insect vectors --- green insecticides --- moth pests --- non-target toxicity --- stored product pests --- termites


Book
Intramolecular Hydrogen Bonding 2021
Author:
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
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Bookmark

Abstract

This book describes the results of both theoretical and experimental research on many topical issues in intramolecular hydrogen bonding. Its great advantage is that the presented research results have been obtained using many different techniques. Therefore, it is an excellent review of these methods, while showing their applicability to the current scientific issues regarding intramolecular hydrogen bonds. The experimental techniques used include X-ray diffraction, infrared and Raman spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), nuclear quadrupole resonance spectroscopy (NQR), incoherent inelastic neutron scattering (IINS), and differential scanning calorimetry (DSC). The solvatochromic and luminescent studies are also described. On the other hand, theoretical research is based on ab initio calculations and the Car–Parrinello Molecular Dynamics (CPMD). In the latter case, a description of nuclear quantum effects (NQE) is also possible. This book also demonstrates the use of theoretical methods such as Quantum Theory of Atoms in Molecules (QTAIM), Interacting Quantum Atoms (IQA), Natural Bond Orbital (NBO), Non-Covalent Interactions (NCI) index, Molecular Tailoring Approach (MTA), and many others.

Keywords

Research & information: general --- intramolecular interaction --- interaction energy --- hydrogen bond --- intramolecular hydrogen bonds --- deuterium isotope effects on chemical shifts --- isotope ratios --- hydrogen bond energies --- intramolecular hydrogen bonding --- high-accuracy extrapolation methods --- QTAIM --- non-covalent interactions --- local vibrational modes --- hydrogen bond (HB) --- intramolecular hydrogen bond (IHB) --- molecular tailoring approach (MTA) --- fragmentation methods --- bond energy estimation --- noncovalent interactions --- structures and binding energies --- charge-transfer interactions --- spin-spin coupling constants --- polymorphism --- isomerization --- phase transition --- nitro group --- matrix isolation --- IINS --- FT-IR --- Raman --- X-ray --- NQR --- DSC --- DFT --- Schiff base --- N-salicylidene aniline derivative --- photophysical properties --- solvatochromism --- Hirshfeld surface analysis --- amino-alcohols --- α-substitution --- beryllium bonds --- calculated infrared spectra --- interacting quantum atoms --- resonance-assisted hydrogen bond --- Schiff bases --- inelastic incoherent neutron scattering --- isotopic effect --- excited-state intramolecular proton transfer --- photochemistry --- photobiology --- quantum chemistry --- molecular dynamics --- ultrafast processes --- gas phase --- crystalline phase --- MP2 --- CCSD --- AIM --- SAPT --- nuclear quantum effects --- CPMD --- intramolecular interaction --- interaction energy --- hydrogen bond --- intramolecular hydrogen bonds --- deuterium isotope effects on chemical shifts --- isotope ratios --- hydrogen bond energies --- intramolecular hydrogen bonding --- high-accuracy extrapolation methods --- QTAIM --- non-covalent interactions --- local vibrational modes --- hydrogen bond (HB) --- intramolecular hydrogen bond (IHB) --- molecular tailoring approach (MTA) --- fragmentation methods --- bond energy estimation --- noncovalent interactions --- structures and binding energies --- charge-transfer interactions --- spin-spin coupling constants --- polymorphism --- isomerization --- phase transition --- nitro group --- matrix isolation --- IINS --- FT-IR --- Raman --- X-ray --- NQR --- DSC --- DFT --- Schiff base --- N-salicylidene aniline derivative --- photophysical properties --- solvatochromism --- Hirshfeld surface analysis --- amino-alcohols --- α-substitution --- beryllium bonds --- calculated infrared spectra --- interacting quantum atoms --- resonance-assisted hydrogen bond --- Schiff bases --- inelastic incoherent neutron scattering --- isotopic effect --- excited-state intramolecular proton transfer --- photochemistry --- photobiology --- quantum chemistry --- molecular dynamics --- ultrafast processes --- gas phase --- crystalline phase --- MP2 --- CCSD --- AIM --- SAPT --- nuclear quantum effects --- CPMD


Book
Insecticide, Acaricide, Repellent and Antimicrobial Development
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

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Bookmark

Abstract

The present book, a reprint of the Molecules Special Issue "Insecticide, Acaricide, Repellent and Antimicrobial Development", presents key advances in the development of effective and eco-friendly insecticides, acaricides, repellents, and antimicrobials, including products of natural origin.

Keywords

Medicine --- Lauraceae --- Aedes aegypti --- Aedes albopictus --- Culex quinquefasciatus --- antibacterial --- antifungal --- antioxidants --- compatibility --- date palm dust mites --- host defense --- Oligonychus afrasiaticus --- Metarhizium anisopliae --- natural acaricide --- synergism --- 1-Chlorooctadecane --- Lamiaceae --- Clinopodium nepeta subsp. nepeta --- Clinopodium nepeta subsp. glandulosum --- essential oils --- chemical variability --- biological activities --- Citrullus colocynthis --- spinasterol, 22,23-dihydrospinasterol --- fernenol --- insecticidal activity --- LC50 --- electrical penetration graph --- peach potato aphid --- antifeedants --- attractants --- structure-activity relationships --- fractionation --- reducing activity --- biomolecules --- antibiofilm --- microbial infection --- mangrove --- larvicidal activity --- enzyme inhibition --- Rhizophora mucronata --- repellent --- mosquitoes --- Erigeron --- Conyza bonariensis --- Conyza canadensis --- Conyza sumatrensis --- mosquito --- vector control --- naphthoquinones --- plumbagin --- Spodoptera littoralis --- insect growth inhibition --- carnivorous plants --- Nepenthes --- botanical-based insecticide --- cereals --- green grain protectant --- essential oil nanoformulation --- stored-product beetles --- Tenebrionidae --- Chagas’ disease transmission --- triatomines --- peridomiciliary use --- Argentina --- biopesticides --- bio-based pesticides --- chemical ecology --- pest control --- natural products --- storage --- monoterpenes --- bioinsecticide --- insect pest --- toxicity --- eugenol derivatives --- amino alcohols --- semisynthetic insecticides --- bioinsecticides --- phenylpropanoids --- Spodoptera frugiperda --- urban pests --- agricultural pests --- aphids --- cockroaches --- kissing bugs --- insect vectors --- green insecticides --- moth pests --- non-target toxicity --- stored product pests --- termites --- n/a --- Chagas' disease transmission


Book
Insecticide, Acaricide, Repellent and Antimicrobial Development
Author:
Year: 2022 Publisher: Basel MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

The present book, a reprint of the Molecules Special Issue "Insecticide, Acaricide, Repellent and Antimicrobial Development", presents key advances in the development of effective and eco-friendly insecticides, acaricides, repellents, and antimicrobials, including products of natural origin.

Keywords

Lauraceae --- Aedes aegypti --- Aedes albopictus --- Culex quinquefasciatus --- antibacterial --- antifungal --- antioxidants --- compatibility --- date palm dust mites --- host defense --- Oligonychus afrasiaticus --- Metarhizium anisopliae --- natural acaricide --- synergism --- 1-Chlorooctadecane --- Lamiaceae --- Clinopodium nepeta subsp. nepeta --- Clinopodium nepeta subsp. glandulosum --- essential oils --- chemical variability --- biological activities --- Citrullus colocynthis --- spinasterol, 22,23-dihydrospinasterol --- fernenol --- insecticidal activity --- LC50 --- electrical penetration graph --- peach potato aphid --- antifeedants --- attractants --- structure-activity relationships --- fractionation --- reducing activity --- biomolecules --- antibiofilm --- microbial infection --- mangrove --- larvicidal activity --- enzyme inhibition --- Rhizophora mucronata --- repellent --- mosquitoes --- Erigeron --- Conyza bonariensis --- Conyza canadensis --- Conyza sumatrensis --- mosquito --- vector control --- naphthoquinones --- plumbagin --- Spodoptera littoralis --- insect growth inhibition --- carnivorous plants --- Nepenthes --- botanical-based insecticide --- cereals --- green grain protectant --- essential oil nanoformulation --- stored-product beetles --- Tenebrionidae --- Chagas’ disease transmission --- triatomines --- peridomiciliary use --- Argentina --- biopesticides --- bio-based pesticides --- chemical ecology --- pest control --- natural products --- storage --- monoterpenes --- bioinsecticide --- insect pest --- toxicity --- eugenol derivatives --- amino alcohols --- semisynthetic insecticides --- bioinsecticides --- phenylpropanoids --- Spodoptera frugiperda --- urban pests --- agricultural pests --- aphids --- cockroaches --- kissing bugs --- insect vectors --- green insecticides --- moth pests --- non-target toxicity --- stored product pests --- termites --- n/a --- Chagas' disease transmission

Kirk-Othmer Encyclopedia of Chemical Technology. Fourth Edition. 16. Volume 16 : Mass transfer to Neuroregulators
Authors: ---
ISBN: 047152669X 0471526703 0471526711 047152672X 0471526746 0471526754 0471526762 0471526770 0471526770 0471526789 0471526800 0471526819 0471526827 0471526827 0471526835 0471526843 0471526851 047152686X 047152686X 0471526878 0471526886 0471526894 0471526908 0471526908 0471526916 0471526924 0471526932 0471526940 0471526940 0471526959 0471526967 9780471238966 0471238961 Year: 1995 Publisher: New York, NY ; Chichester : John Wiley,

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Abstract

"Written by prominent scholars from industry, academia, and research institutions, the Kirk-Othmer Encyclopedia of Chemical Technology presents a wide scope of articles on chemical substances—including their properties, manufacturing, and uses. It also focuses on industrial processes and unit operations in chemical engineering, as well as covering fundamentals and scientific subjects related to the field. Additionally, environmental and health issues concerning chemical technology are also addressed."--About page

Keywords

Chemistry, Technical --- Chemistry [Technical ] --- Encyclopedias --- Chemical technologies --- Chemistry, Technical. --- ENCYCLOPEDIAS --- Chemical technology --- Industrial chemistry --- Technical chemistry --- Chemistry --- Technology --- Chemical engineering --- Monograph --- Chemical Engineering --- Chemical & Materials Engineering --- Engineering & Applied Sciences --- Optical detectors. --- Patents. --- Petroleum. --- Gases. --- Materials. --- Microbiology. --- Nanoparticles. --- Optical rotation. --- Aquaculture --- Coal. --- Coating processes. --- Coatings. --- Colloids. --- Combustion --- Glass. --- Information science. --- Infrared spectroscopy. --- Insects. --- Ion exchange. --- Iron compounds. --- Ketones. --- Laboratories. --- Raman spectroscopy. --- Rare earth metal compounds. --- Immunoassay. --- Immunochemistry. --- Carbohydrates. --- Heat --- Mass transfer. --- Disinfection. --- Transmission. --- Computer software. --- Cosmetics. --- Databases. --- Composites --- Ceramics. --- Fuel. --- Genetic engineering. --- Heat exchangers. --- Nuclear fusion. --- Digestive System. --- Growth Substances. --- Géotextiles --- Lasers. --- Lead compounds. --- Lead. --- Light. --- Liquids. --- Manganese compounds. --- Mass spectrometry. --- Nuclear magnetic resonance. --- Marketing --- Actinide elements. --- Adsorption --- Aérosols --- Pollution atmosphérique --- Chemistry, Forensic. --- Flotation. --- Fluid mechanics. --- Fluidization. --- Fluorine compounds. --- Fluorine. --- Food additives. --- Food contamination. --- Food handling. --- Fuel cells. --- Digestive System --- Growth Substances --- Disinfection --- Benzene, ethenyl --- Benzene, ethenyl, polymers --- Butanedioic acid --- Dyes --- Microgravity --- Particle size --- Pesticides --- Silicon compounds --- Silk --- Silver --- Silver compounds --- Soaps --- Sodium --- Sodium compounds --- Soil --- Sol-gel processing --- Solar energy --- Solders --- Solvents --- Soybeans --- Spectroscopy --- Sprays --- Stains (coloring materials) --- Starches --- Steam --- Steel --- Steroids --- Stimulants (nervous systems) --- Strontium --- Strontium compounds --- Styrene-butadiene rubber --- Fungicides --- Furnaces --- Gallium --- Gallium compounds --- Gasoline --- Gelatins --- Gemstones --- Geothermal energy --- Germanium --- Germanium compounds --- Glycerol --- Glycols --- Gold --- Gold compounds --- Grignard reaction --- Gums --- Hafnium --- Hafnium compounds --- Hair preparations --- Hardness (mechanical) --- Heat resistant materials --- Heat stabilizers --- Metallic glasses --- Natural gas --- Safety --- Synthetic fuels --- Waters, natural --- 1,3-butadiene, 2-methyl --- Biocides --- Butanedioic acid, methylene --- -Catalysis --- Electric insulators --- Ethenone derivatives --- Hypoglycemic agents --- Imines --- Incinerators --- Inclusion compounds --- Indium --- Indium compounds --- Indole derivatives --- Industrial hygiene --- Inks --- Inorganic polymers --- Integrated circuits --- Iodine --- Iodine compounds --- Ion implantation --- Ionomers --- Iron --- Isocyanates --- Plastics, laminated --- Reaction kinetics --- Sound insulators --- Thermal insulators --- 2-butenedioic acid (z) --- Brown coal --- Esr (electron spin resonance) --- Latex --- Leather --- Lecithins --- Lignins --- Lime --- Limestone --- Liquefied petroleum gases --- Liquid crystals --- Lithium --- Lithium compounds --- Lubricants --- Lubrication --- Luminescent materials --- Machining --- Magnesium --- Magnesium compounds --- Magnetic substances --- Magnetohydrodynamics --- Malt --- Manganese --- Propanedioic acid --- 1,2,3-propanetricarboxylic acid, 2-hydroxy --- -2-propenoic acid, 3-phenyl --- Chloro hydrocarbons --- Chlorosulfuric acid --- Chocolate --- Choline --- Chromatography --- Chromium --- Chromium compounds --- Chromophores --- Cobalt --- Cobalt compounds --- Coffee (beverage) --- Color --- Coloring materials --- Hydroxy compounds --- Phenols --- Photography --- 2h-1-benzopyran-2-one --- Antifoaming agents --- Benzene, 1-methylethyl --- Contact lenses --- Contraceptive agents --- Controlled-release drug delivery systems --- Coordination compounds --- Copper --- Copper compounds --- Corrosion --- Cotton fibers --- Cryogenics --- Crystallization --- Cyanamide derivatives --- Cyanides (inorganic) --- Cyanine dyes --- Cyanohydrins --- Cyanuric acid --- Cyclohexane derivatives --- Cyclopentadiene --- Dairy products --- Dental materials --- Detergency --- Drying agents --- Laboratory experiment --- Nitriles --- 2-propanone --- 2-propenal --- Ablative materials --- Abrasives --- Absorption --- Acetic acid --- Acrylic polymers --- Adhesives --- Aeration --- Air conditioning --- Alcohols --- Aldehydes --- Alkali metal hydroxides --- Alkaloids --- Ethyne derivatives --- Hexanedioic acid --- Polyoxymethylenes --- Adrenal cortex hormones --- Aerogels --- Benzene, dimethyl --- Biopolymers --- Bioremediation --- Chirality --- Condensation (physical) --- Furans --- Microemulsions --- Molecular modeling --- Molecular recognition --- Photoresists --- Purity --- Recycling of polymeric materials --- Semiconductor compounds --- Separation --- Surface analysis --- Thermography --- Urea --- Water-soluble polymers --- Weighing --- Welding --- Wine --- Wood --- ANTIBIOTICS --- ANTI-OBESITY AGENTS --- ANTIFREEZE --- ANTIMONY --- ANTIMONY COMPOUNDS --- ANTIOXIDANTS --- ANTIOZONANTS --- PARASITICIDES --- ANTISTATIC AGENTS --- VIRUCIDES --- AQUACULTURE --- ARSENIC --- ARSENIC COMPOUNDS --- ASBESTOS --- ASPHALT --- AIR POLLUTION --- INSTRUMENTATION --- JET AIRCRAFT FUEL --- DYES --- BAKERY PRODUCTS --- BARIUM --- BARIUM COMPOUNDS --- POLYMERS --- PERMEABILITY --- FUEL CELLS --- PROPERTIES --- 9,10-anthracenedione --- Alcohols, compounds, metal salts --- Alkyd resins --- Alkylation --- Allylic compounds --- Aluminum --- Aluminum compounds --- Amides --- Amines --- Amino acids --- Amino alcohols --- Aminoplasts --- Ammonia --- Ammonium compounds --- Analgesics --- Analytical chemistry --- Anesthetics --- Antibacterial agents --- Antibiotics --- Bronchodilator agents --- Senescence --- POWER --- PRESSURE --- PRINTING --- PROCESS CONTROL AND DYNAMICS --- ENERGY CONSERVATION --- PRODUCT LIABILITY --- 1-PROPANOL --- 2-PROPANOL --- OXIRANE, METHYL --- PROSTAGLANDINS --- PROSTHETIC DEVICES --- PROTEINS --- PSYCHOTROPIC DRUGS --- PULP (CELLULOSE) --- PUMPS --- PYRAZOLE DERIVATIVES --- PYRIDINE DERIVATIVES --- PYROTECHNIC COMPOSITIONS --- PYRROLE DERIVATIVES --- QUALITY CONTROL --- QUATERNARY AMMONIUM COMPOUNDS --- QUINOLINE DERIVATIVES --- QUINONES --- CROSSLINKING AGENTS --- RADIATION --- ISOTOPE INDICATORS --- RADIOELEMENTS --- RADIOGRAPHY, CONTRAST AGENTS --- PHARMACEUTICALS, RADIO --- RADIOPROTECTANTS --- REACTORS --- COATINGS --- RECYCLING --- CHEMICAL AND PHYSICAL EFFECTS --- MATCHES --- MATERIALS --- STANDARDS --- MEAT PRODUCTS --- DIAGNOSIS --- DIAGNOSTIC IMAGING --- MEMBRANES --- MEMORY, BIOLOGICAL --- MERCURY --- MERCURY COMPOUNDS --- ANODES --- METALS --- METALLURGY --- COMPOSITES --- SURFACE (CHEMISTRY AND PHYSICS) --- 2-PROPENOIC ACID, 2-METHYL --- METHANOL --- MICA-GROUP MINERALS --- POLYSACCHARIDES, BACTERIAL --- METABOLISM (MICROBIAL) --- MICROENCAPSULATION --- MICROSCOPY --- MICROWAVE --- MILK --- DAIRY PRODUCTS --- MINERAL ELEMENTS --- NUTRIENTS --- MINERALS --- MIXING --- MOLECULAR SIEVES --- MOLYBDENUM --- MOLYBDENUM COMPOUNDS --- NAPHTHALENE DERIVATIVES --- NAPHTHENIC ACIDS --- NEUROHORMONES --- NEUROTRANSMITTER AGONISTS --- NEUROTRANSMITTER ANTAGONISTS --- PREPARATION --- 1,2-benzenedicarboxylic acid --- Carbonic dichloride --- Disperse systems --- Paper --- Perchloric acid --- Perfumes --- Peroxides --- Pharmaceutical preparations --- Phenolic resins --- Phosphates --- Phosphine derivatives --- Phosphoric acid --- Phosphorus --- Phosphorus compounds --- Photochemistry --- Photoconductivity --- Photoelectric devices --- Phthalocyanine compounds --- Pigments --- THIOGLYCOLIC ACID --- THIOLS --- THIOPHENE DERIVATIVES --- THIOSULFATES --- THORIUM --- THORIUM COMPOUNDS --- THYROID GLAND --- THYROID HORMONES --- TIN --- TIN ALLOYS --- TIN COMPOUNDS --- TIRES --- TITANIUM --- TITANIUM ALLOYS --- TITANIUM COMPOUNDS --- TOLUENE --- TOXICOLOGY --- TRACE ELEMENTS --- TRANSPORTATION --- TUNGSTEN --- TUNGSTEN ALLOYS --- TUNGSTEN COMPOUNDS --- ULTRAFILTRATION --- UNITS OF MEASUREMENT --- URANIUM --- URANIUM COMPOUNDS --- THALLIUM COMPOUNDS --- POLYURETHANES --- VACCINES --- VACUUM --- VANADIUM --- VANADIUM ALLOYS --- VANADIUM COMPOUNDS --- VANILLIN --- VETERINARY MEDICINE --- VINEGAR --- VINYL COMPOUNDS --- VINYL POLYMERS --- ANALYSIS --- 1,1'-biphenyl, deriv --- Alcoholic beverages --- Alkadienes --- Aromatic hydrocarbons --- Bearings --- Beer --- Benzene --- Beryllium --- Biotechnology --- Bismuth --- Bleaching agents --- Blood --- Boron --- Bromine --- Cadmium --- Calcium --- Carbides --- Carbon --- Construction materials --- Friction materials --- Alditols --- Films (physical chemistry) --- S-substitution --- Sulfamic acid --- Sulfolane --- Sulfonation --- Sulfonic acids --- Sulfoxides --- Sulfur --- Sulfur compounds --- Sulfuric acid --- Supercritical fluids --- Surfactants --- Sutures --- Sweetening agents --- Talc --- Tall oil --- Tanks (containers) --- Tantalum --- Tantalum compounds --- Tar --- Tea --- Tellurium --- Tellurium compounds --- Temperature sensors --- Terpenes --- Textiles --- Thallium --- Thallium compounds --- Thermodynamics --- Thermoelectricity --- Anemometers --- Blood chemical analysis --- Flavoring agents --- Flocculating agents --- Fluorescent brighteners --- Foams --- Formaldehyde --- Formic acid --- Fractionation --- Fracture (materials) --- Friedel-crafts reaction --- Fruit and vegetable juices --- Plastics, cellular --- Viscosimeters

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