An actinometer is an instrument that can measure the heating power of radiation. Actinometers are used in meteorology to measure solar radiation as pyranometers, pyrheliometers and net radiometers.
An actinometer is a chemical system or physical device which determines the number of photons in a beam integrally or per unit time. This name is commonly applied to devices used in the ultraviolet and visible wavelength ranges. For example, solutions of iron(III) oxalate can be used as a chemical actinometer, while bolometers, thermopiles, and photodiodes are physical devices giving a reading that can be correlated to the number of photons detected.
Swiss physicist Horace-Bénédict de Saussure invented an early version in the late 18th century. His design used a blackened thermometer enclosed in a glass sphere to measure solar radiation, which he referred to as a "heliothermometer." This instrument is considered one of the first tools to systematically measure solar intensity.
John Herschel further developed actinometers in the 19th century, including a design involving photochemical reactions to measure sunlight intensity, which was a significant step forward. Herschel's actinometer involved observing the rate of a chemical reaction under sunlight, which allowed for more precise quantification of solar energy. Herschel's version was influential and helped standardize measurements of solar energy. Herschel introduced the term actinometer, the first of many uses of the prefix actin for scientific instruments, effects, and processes. [1]
The actinograph is a related device for estimating the actinic power of lighting for photography.
Chemical actinometry involves measuring radiant flux via the yield from a chemical reaction. This process requires a chemical with a known quantum yield and easily analyzed reaction products.
Potassium ferrioxalate is commonly used, as it is simple to use and sensitive over a wide range of relevant wavelengths (254 nm to 500 nm). Other actinometers include malachite green Leucocyanidins, vanadium(V)–iron(III) oxalate and monochloroacetic acid, however all of these actinometers undergo dark reactions, that is, they react in the absence of light. This is undesirable since it will have to be corrected for. Organic actinometers like butyrophenone or piperylene are analysed by gas chromatography. Other actinometers are more specific in terms of the range of wavelengths at which quantum yields have been determined. Reinecke's salt K[Cr(NH3)2(NCS)4] reacts in the near-UV region although it is thermally unstable. [2] [3] [4] Uranyl oxalate has been used historically but is very toxic and cumbersome to analyze.
Recent investigations into nitrate photolysis [5] [6] have used 2-nitrobenzaldehyde and benzoic acid as a radical scavenger for hydroxyl radicals produced in the photolysis of hydrogen peroxide and sodium nitrate. However, they originally used ferrioxalate actinometry to calibrate the quantum yields for the hydrogen peroxide photolysis. Radical scavengers proved a viable method of measuring production of hydroxyl radical.
Meso-diphenylhelianthrene can be used for chemical actinometry in the visible range (400–700 nm). [7] This chemical measures in the 475–610 nm range, but measurements in wider spectral ranges can be done with this chemical if the emission spectrum of the light source is known.
Photochemistry is the branch of chemistry concerned with the chemical effects of light. Generally, this term is used to describe a chemical reaction caused by absorption of ultraviolet, visible (400–750 nm), or infrared radiation (750–2500 nm).
Photobiology is the scientific study of the beneficial and harmful interactions of light in living organisms. The field includes the study of photophysics, photochemistry, photosynthesis, photomorphogenesis, visual processing, circadian rhythms, photomovement, bioluminescence, and ultraviolet radiation effects.
The ozone–oxygen cycle is the process by which ozone is continually regenerated in Earth's stratosphere, converting ultraviolet radiation (UV) into heat. In 1930 Sydney Chapman resolved the chemistry involved. The process is commonly called the Chapman cycle by atmospheric scientists.
In particle physics, the quantum yield of a radiation-induced process is the number of times a specific event occurs per photon absorbed by the system.
Photosensitizers are light absorbers that alter the course of a photochemical reaction. They usually are catalysts. They can function by many mechanisms, sometimes they donate an electron to the substrate, sometimes they abstract a hydrogen atom from the substrate. At the end of this process, the photosensitizer returns to its ground state, where it remains chemically intact, poised to absorb more light. One branch of chemistry which frequently utilizes photosensitizers is polymer chemistry, using photosensitizers in reactions such as photopolymerization, photocrosslinking, and photodegradation. Photosensitizers are also used to generate prolonged excited electronic states in organic molecules with uses in photocatalysis, photon upconversion and photodynamic therapy. Generally, photosensitizers absorb electromagnetic radiation consisting of infrared radiation, visible light radiation, and ultraviolet radiation and transfer absorbed energy into neighboring molecules. This absorption of light is made possible by photosensitizers' large de-localized π-systems, which lowers the energy of HOMO and LUMO orbitals to promote photoexcitation. While many photosensitizers are organic or organometallic compounds, there are also examples of using semiconductor quantum dots as photosensitizers.
Photodissociation, photolysis, photodecomposition, or photofragmentation is a chemical reaction in which molecules of a chemical compound are broken down by absorption of light or photons. It is defined as the interaction of one or more photons with one target molecule that dissociates into two fragments.
Photodegradation is the alteration of materials by light. Commonly, the term is used loosely to refer to the combined action of sunlight and air, which cause oxidation and hydrolysis. Often photodegradation is intentionally avoided, since it destroys paintings and other artifacts. It is, however, partly responsible for remineralization of biomass and is used intentionally in some disinfection technologies. Photodegradation does not apply to how materials may be aged or degraded via infrared light or heat, but does include degradation in all of the ultraviolet light wavebands.
UV filters are compounds, mixtures, or materials that block or absorb ultraviolet (UV) light. One of the major applications of UV filters is their use as sunscreens to protect skin from sunburn and other sun/UV related damage. After the invention of digital cameras changed the field of photography, UV filters have been used to coat glass discs fitted to camera lenses to protect hardware that is sensitive to UV light.
Organic photochemistry encompasses organic reactions that are induced by the action of light. The absorption of ultraviolet light by organic molecules often leads to reactions. In the earliest days, sunlight was employed, while in more modern times ultraviolet lamps are employed. Organic photochemistry has proven to be a very useful synthetic tool. Complex organic products can be obtained simply.
Potassium ferrioxalate, also called potassium trisoxalatoferrate or potassium tris(oxalato)ferrate(III) is a chemical compound with the formula K3[Fe(C2O4)3]. It often occurs as the trihydrate K3[Fe(C2O4)3]·3H2O. Both are crystalline compounds, lime green in colour.
In chemistry, a photoinitiator is a molecule that creates reactive species when exposed to radiation. Synthetic photoinitiators are key components in photopolymers.
The photostationary state of a reversible photochemical reaction is the equilibrium chemical composition under a specific kind of electromagnetic irradiation.
In polymer chemistry photo-oxidation is the degradation of a polymer surface due to the combined action of light and oxygen. It is the most significant factor in the weathering of plastics. Photo-oxidation causes the polymer chains to break, resulting in the material becoming increasingly brittle. This leads to mechanical failure and, at an advanced stage, the formation of microplastics. In textiles the process is called phototendering.
Nitrogen trioxide or nitrate radical is an oxide of nitrogen with formula NO
3, consisting of three oxygen atoms covalently bound to a nitrogen atom. This highly unstable blue compound has not been isolated in pure form, but can be generated and observed as a short-lived component of gas, liquid, or solid systems.
Photoelectrochemical processes are processes in photoelectrochemistry; they usually involve transforming light into other forms of energy. These processes apply to photochemistry, optically pumped lasers, sensitized solar cells, luminescence, and photochromism.
Non-ionizingradiation refers to any type of electromagnetic radiation that does not carry enough energy per quantum to ionize atoms or molecules—that is, to completely remove an electron from an atom or molecule. Instead of producing charged ions when passing through matter, non-ionizing electromagnetic radiation has sufficient energy only for excitation. Non-ionizing radiation is not a significant health risk. In contrast, ionizing radiation has a higher frequency and shorter wavelength than non-ionizing radiation, and can be a serious health hazard: exposure to it can cause burns, radiation sickness, many kinds of cancer, and genetic damage. Using ionizing radiation requires elaborate radiological protection measures, which in general are not required with non-ionizing radiation.
A photooxygenation is a light-induced oxidation reaction in which molecular oxygen is incorporated into the product(s). Initial research interest in photooxygenation reactions arose from Oscar Raab's observations in 1900 that the combination of light, oxygen and photosensitizers is highly toxic to cells. Early studies of photooxygenation focused on oxidative damage to DNA and amino acids, but recent research has led to the application of photooxygenation in organic synthesis and photodynamic therapy.
Photogeochemistry merges photochemistry and geochemistry into the study of light-induced chemical reactions that occur or may occur among natural components of Earth's surface. The first comprehensive review on the subject was published in 2017 by the chemist and soil scientist Timothy A Doane, but the term photogeochemistry appeared a few years earlier as a keyword in studies that described the role of light-induced mineral transformations in shaping the biogeochemistry of Earth; this indeed describes the core of photogeochemical study, although other facets may be admitted into the definition.
A photolabile protecting group is a chemical modification to a molecule that can be removed with light. PPGs enable high degrees of chemoselectivity as they allow researchers to control spatial, temporal and concentration variables with light. Control of these variables is valuable as it enables multiple PPG applications, including orthogonality in systems with multiple protecting groups. As the removal of a PPG does not require chemical reagents, the photocleavage of a PPG is often referred to as "traceless reagent processes", and is often used in biological model systems and multistep organic syntheses. Since their introduction in 1962, numerous PPGs have been developed and utilized in a variety of wide-ranging applications from protein science to photoresists. Due to the large number of reported protecting groups, PPGs are often categorized by their major functional group(s); three of the most common classifications are detailed below.
Ferrioxalate or trisoxalatoferrate(III) is a trivalent anion with formula [Fe(C2O4)3]3−. It is a transition metal complex consisting of an iron atom in the +3 oxidation state and three bidentate oxalate ions C2O2−4 anions acting as ligands.