Lightfastness

Last updated
Clay earth pigments such as burnt sienna often have a high lightfastness Pigment sienna burnt iconofile.jpg
Clay earth pigments such as burnt sienna often have a high lightfastness

Lightfastness is a property of a colourant such as dye or pigment that describes its resistance to fading when exposed to light. [1] [2] [3] Dyes and pigments are used for example for dyeing of fabrics, plastics or other materials and manufacturing paints or printing inks.

Contents

The bleaching of the color is caused by the impact of ultraviolet radiation in the chemical structure of the molecules giving the color of the subject. The part of a molecule responsible for its color is called the chromophore. [4] [5]

Light encountering a painted surface can either alter or break the chemical bonds of the pigment, causing the colors to bleach or change in a process known as photodegradation. [6] Materials that resist this effect are said to be lightfast. The electromagnetic spectrum of the sun contains wavelengths from gamma waves to radio waves. The high energy of ultraviolet radiation in particular accelerates the fading of the dye. [7]

The photon energy of UVA-radiation which is not absorbed by atmospheric ozone exceeds the dissociation energy of the carbon-carbon single bond, resulting in the cleavage of the bond and fading of the color. [7] Inorganic colourants are considered to be more lightfast than organic colourants. [8] Black colourants are usually considered the most lightfast. [9]

Lightfastness is measured by exposing a sample to a lightsource for a predefined period of time and then comparing it to an unexposed sample. [2] [3] [10]

Chemical processes

During the fading, colourant molecules undergo various chemical processes which result in fading.

When a UV-photon reacts with a molecule acting as colourant, the molecule is excited from the ground state to an excited state. The excited molecule is highly reactive and unstable. During the quenching of the molecule from excited state to ground state, atmospheric triplet oxygen reacts with the colourant molecule to form singlet oxygen and superoxide oxygen radical. The oxygen atom and the superoxide radical resulting from the reaction are both highly reactive and capable of destroying the colourants. [7]

Photolysis

Photolysis, i.e., photochemical decomposition is a chemical reaction where the compound is broken down by the photons. This decomposition occurs when a photon of sufficient energy encounters a colorant molecule bond with a suitable dissociation energy. The reaction causes homolytic cleavage in the chromophoric system resulting in the fading of the colourant. [7]

Photo-oxidation

Photo-oxidation, i.e., photochemical oxidation. A colorant molecule, when excited by a photon of sufficient energy, undergoes an oxidation process. In the process the chromophoric system of the colorant molecule reacts with the atmospheric oxygen to form a non-chromophoric system, resulting in fading. Colorants which contain a carbonyl group as the chromophore are particularly vulnerable to oxidation. [7]

Photoreduction

Photo-reduction, i.e., photochemical reduction. A colorant molecule with an unsaturated double bond (typical to alkenes) or triple bond (typical to alkynes) acting as a chromophore undergoes reduction in the presence of hydrogen and photons of sufficient energy, forming a saturated chromophoric system. Saturation reduces the length of the chromophoric system, resulting in the fading of the colorant. [7]

Photosensitization

Photosensitization, i.e., photochemical sensitization. Exposing dyed cellulosic material, such as plant-based fibers, to sunlight allows dyes to remove hydrogen from the cellulose, resulting in photoreduction on the cellulosic substrate. Simultaneously, the colorant will undergo oxidation in the presence of the atmospheric oxygen, resulting in photo-oxidation of the colourant. These processes result in both fading of the colorant and strength loss of the substrate. [7]

Phototendering

Phototendering, i.e., photochemical tendering. As a result of UV light, the substrate material supplies hydrogen to the colourant molecules, reducing the colorant molecule. As the hydrogen is removed, the material undergoes oxidation. [7]

Standards and measure scales

Some organizations publish standards for rating the lightfastness of pigments and materials. Testing is typically done by controlled exposure to sunlight, or to artificial light generated by a xenon arc lamp. [11] Watercolors, inks, pastels, and colored pencils are particularly susceptible to fading over time, so choosing lightfast pigments is especially important in these media. [1]

The most well known scales measuring the lightfastness are the Blue Wool Scale, Grey scale and the scale defined by ASTM (American Standard Test Measure). [11] [12] [13] [14] On the Blue Wool Scale the lightfastness is rated between 1–8. 1 being very poor and 8 being excellent lightfastness. In grey scale the lightfastness is rated between 1–5. 1 being very poor and 5 being excellent lightfastness. [1] [2] [10] On ASTM scale the lightfastness is rated between I-V. I is excellent lightfastness and it corresponds to ratings 7–8 on Blue Wool Scale. V is very poor lightfastness and it corresponds to Blue Wool scale rating 1. [10]

Metropolia sign bleached.jpg
Side of a sign of the University of Applied Sciences oriented towards the southeast where direct sunlight impacting from dawn to afternoon has bleached the red and yellow colors from the logo of the institution.
Metropolia sign unbleached.jpg
Side of the sign oriented towards the northwest where the red and yellow colors can still be clearly recognized.

The actual lightfastness is dependent on the strength of the radiation of the sun, so lightfastness is relative to geographic location, season, and exposure direction. The following table is listing suggestive relations of the lightfastness ratings on different measure scales and the relation relative to time in direct sunlight and normal conditions of display: away from a window, under indirect sunlight and properly framed behind a UV protective glass. [10]

DescriptionMeasure scalesDirect exposureNormal conditions of display
Blue Wool ratingASTM ratingSummerWinter
Very poor lightfastness1Vless than 2 years
Poor lightfastness2IV2–15 years
34–8 days2–4 weeks
Fair lightfastness4III2–3 weeks2–3 months15–50 years
53–5 weeks4–5 months
Very good lightfastness6II6–8 weeks5–6 months50–100 years
Excellent lightfastness7I3–4 months7–9 monthsover 100 years
8over 1.5 years

Test procedure

The relative amount of fading can be measured and studied by using standard test strips. In the workflow of the Blue Wool test, one reference strip set shall be stored protected from any exposure to light. Simultaneously, another equivalent test strip set is exposed under a light source defined in the standard. For example, if the lightfastness of the colourant is indicated to be 5 on the Blue Wool scale, it can be expected to fade by a similar amount as the strip number 5 in the Blue Wool test strip set. The success of the test can be confirmed by comparing the test strip set with the reference set that was stored protected from the light. [12] [13]

In graphical industry

In printing, organic pigments are mainly used in the inks, so the shifting or bleaching of the color of a printing product due to the presence of UV light is usually just a matter of time. The use of organic pigments is justified primarily by their inexpensive cost compared to inorganic pigments. The particle size of the inorganic pigments is often larger than that of organic pigments, thus inorganic pigments are often not suitable to be used in offset printing. [15]

In screen printing, the particle size of the pigment is not the limiting factor. Thus it is the preferred printing method for printing jobs requiring extreme lightfastness. The thickness of the ink layer affects the lightfastness by the amount of pigment laid on the substrate. The ink layer printed by screen printing is thicker than that printed by offset printing. In other words, it contains more pigment per area. This leads to better lightfastness even though the printing ink used in both methods would be based on the same pigment. [7]

When mixing printing inks, the ink with the weaker lightfastness defines the lightfastness of the whole mixed color. The fading of one of the pigments leads to a tone shift towards the component with better lightfastness. If it is required that there will be something visible from the printing, even though its dominant pigment would fade, then a small amount of pigment with excellent lightfastness can be mixed with it.

See also

Related Research Articles

<span class="mw-page-title-main">Dye</span> Soluble chemical substance or natural material which can impart color to other materials

A dye is a colored substance that chemically bonds to the substrate to which it is being applied. This distinguishes dyes from pigments which do not chemically bind to the material they color. Dye is generally applied in an aqueous solution and may require a mordant to improve the fastness of the dye on the fiber.

<span class="mw-page-title-main">Ink</span> Liquid or paste that contains pigments or dyes

Ink is a gel, sol, or solution that contains at least one colorant, such as a dye or pigment, and is used to color a surface to produce an image, text, or design. Ink is used for drawing or writing with a pen, brush, reed pen, or quill. Thicker inks, in paste form, are used extensively in letterpress and lithographic printing.

<span class="mw-page-title-main">Pigment</span> Colored material

A pigment is a powder used to add color or change visual appearance. Pigments are completely or nearly insoluble and chemically unreactive in water or another medium; in contrast, dyes are colored substances which are soluble or go into solution at some stage in their use. Dyes are often organic compounds whereas pigments are often inorganic. Pigments of prehistoric and historic value include ochre, charcoal, and lapis lazuli.

A colourant/colour additive or colorant/color additive is a substance that is added or applied in order to change the colour of a material or surface. Colourants can be used for many purposes including printing, painting, and for colouring many types of materials such as foods and plastics. Colourants work by absorbing varying amounts of light at different wavelengths of its spectrum, transmitting or reflecting the remaining light in straight lines or scattered.

<span class="mw-page-title-main">Dyeing</span> Process of adding color to textile products

Dyeing is the application of dyes or pigments on textile materials such as fibers, yarns, and fabrics with the goal of achieving color with desired color fastness. Dyeing is normally done in a special solution containing dyes and particular chemical material. Dye molecules are fixed to the fiber by absorption, diffusion, or bonding with temperature and time being key controlling factors. The bond between the dye molecule and fiber may be strong or weak, depending on the dye used. Dyeing and printing are different applications; in printing, color is applied to a localized area with desired patterns. In dyeing, it is applied to the entire textile.

In chemistry, chromism is a process that induces a change, often reversible, in the colors of compounds. In most cases, chromism is based on a change in the electron states of molecules, especially the π- or d-electron state, so this phenomenon is induced by various external stimuli which can alter the electron density of substances. It is known that there are many natural compounds that have chromism, and many artificial compounds with specific chromism have been synthesized to date. It is usually synonymous with chromotropism, the (reversible) change in color of a substance due to the physical and chemical properties of its ambient surrounding medium, such as temperature and pressure, light, solvent, and presence of ions and electrons.

<span class="mw-page-title-main">Indanthrone blue</span> Organic dye made from 2-aminoanthraquinone

Indanthrone blue, also called indanthrene, is an organic compound with the formula (C14H6O2NH)2. It is a dark blue solid that is a common dye as well as a precursor to other dyes.

<span class="mw-page-title-main">Acid dye</span> Dye applied to low pH textile

An acid dye is a dye that is typically applied to a textile at low pH. They are mainly used to dye wool, not cotton fabrics. Some acid dyes are used as food colorants, and some can also be used to stain organelles in the medical field.

<span class="mw-page-title-main">Chromophore</span> A molecule that absorbs light

A chromophore is a molecule which absorbs light at a particular wavelength and emits color as a result. Chromophores are commonly referred to as colored molecules for this reason. The word is derived from Ancient Greek χρῶμᾰ (chroma) 'color', and -φόρος (phoros) 'carrier of'. Many molecules in nature are chromophores, including chlorophyll, the molecule responsible for the green colors of leaves. The color that is seen by our eyes is that of the light not absorbed by the reflecting object within a certain wavelength spectrum of visible light. The chromophore indicates a region in the molecule where the energy difference between two separate molecular orbitals falls within the range of the visible spectrum. Visible light that hits the chromophore can thus be absorbed by exciting an electron from its ground state into an excited state. In biological molecules that serve to capture or detect light energy, the chromophore is the moiety that causes a conformational change in the molecule when hit by light.

The Blue Wool Scale measures and calibrates the permanence of colouring dyes. Traditionally this test was developed for the textiles industry but it has now been adopted by the printing industry as measure of lightfastness of ink colourants. The American Association of Textile Chemists and Colorists pioneered the work on these test methods and together with the ASTM D13 committee.

<span class="mw-page-title-main">Photochromism</span> Reversible chemical transformation by absorption of electromagnetic radiation

Photochromism is the reversible change of color upon exposure to light. It is a transformation of a chemical species (photoswitch) between two forms by the absorption of electromagnetic radiation (photoisomerization), where the two forms have different absorption spectra.

Photodissociation, photolysis, photodecomposition, or photofragmentation is a chemical reaction in which molecules of a chemical compound are broken down by photons. It is defined as the interaction of one or more photons with one target molecule.

<span class="mw-page-title-main">Photodegradation</span> Alteration of materials by light

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.

Photoprotection is the biochemical process that helps organisms cope with molecular damage caused by sunlight. Plants and other oxygenic phototrophs have developed a suite of photoprotective mechanisms to prevent photoinhibition and oxidative stress caused by excess or fluctuating light conditions. Humans and other animals have also developed photoprotective mechanisms to avoid UV photodamage to the skin, prevent DNA damage, and minimize the downstream effects of oxidative stress.

Digital textile printing is described as any ink jet based method of printing colorants onto fabric. Most notably, digital textile printing is referred to when identifying either printing smaller designs onto garments and printing larger designs onto large format rolls of textile. The latter is a growing trend in visual communication, where advertisement and corporate branding is printed onto polyester media. Examples are: flags, banners, signs, retail graphics.

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.

Colour fastness is a term—used in the dyeing of textile materials—that characterizes a material's colour's resistance to fading or running. Colour fastness is the property of dyes and it is directly proportional to the binding force between photochromic dye and the fibre. The colour fastness may also be affected by processing techniques and choice of chemicals and auxiliaries.

Wet Processing Engineering is one of the major streams in Textile Engineering or Textile manufacturing which refers to the engineering of textile chemical processes and associated applied science. The other three streams in textile engineering are yarn engineering, fabric engineering, and apparel engineering. The processes of this stream are involved or carried out in an aqueous stage. Hence, it is called a wet process which usually covers pre-treatment, dyeing, printing, and finishing.

Light harvesting materials harvest solar energy that can then be converted into chemical energy through photochemical processes. Synthetic light harvesting materials are inspired by photosynthetic biological systems such as light harvesting complexes and pigments that are present in plants and some photosynthetic bacteria. The dynamic and efficient antenna complexes that are present in photosynthetic organisms has inspired the design of synthetic light harvesting materials that mimic light harvesting machinery in biological systems. Examples of synthetic light harvesting materials are dendrimers, porphyrin arrays and assemblies, organic gels, biosynthetic and synthetic peptides, organic-inorganic hybrid materials, and semiconductor materials. Synthetic and biosynthetic light harvesting materials have applications in photovoltaics, photocatalysis, and photopolymerization.

<span class="mw-page-title-main">Synthetic colorant</span>


A colorant is any substance that changes the spectral transmittance or reflectance of a material. Synthetic colorants are those created in a laboratory or industrial setting. The production and improvement of colorants was a driver of the early synthetic chemical industry, in fact many of today's largest chemical producers started as dye-works in the late 19th or early 20th centuries, including Bayer AG(1863). Synthetics are extremely attractive for industrial and aesthetic purposes as they have they often achieve higher intensity and color fastness than comparable natural pigments and dyes used since ancient times. Market viable large scale production of dyes occurred nearly simultaneously in the early major producing countries Britain (1857), France (1858), Germany (1858), and Switzerland (1859), and expansion of associated chemical industries followed. The mid-nineteenth century through WWII saw an incredible expansion of the variety and scale of manufacture of synthetic colorants. Synthetic colorants quickly became ubiquitous in everyday life, from clothing to food. This stems from the invention of industrial research and development laboratories in the 1870s, and the new awareness of empirical chemical formulas as targets for synthesis by academic chemists. The dye industry became one of the first instances where directed scientific research lead to new products, and the first where this occurred regularly.

References

  1. 1 2 3 Boddy-Evans, Marion. "Art Glossary: Lightfastness". About.com . Retrieved 5 March 2015.
  2. 1 2 3 Simmons, Rosemary (2002). Dictionary of Printmaking Terms. London: A & C Black (Publishers) Ltd. p. 30. ISBN   978-0-7136-5795-1.
  3. 1 2 "Lightfastness". Printwiki. Retrieved 6 February 2017.
  4. "IUPAC Gold Book: Chromophore". IUPAC – International Union of Pure and Applied Chemistry. doi:10.1351/goldbook.C01076 . Retrieved 6 February 2017.
  5. Mälkönen, Pentti (1979). Orgaaninen kemia (in Finnish). Otava. pp. 237–238. ISBN   978-951-1-05378-1.
  6. "Why does ultraviolet light cause colors to fade?". Library of Congress. 23 August 2010. Retrieved 5 March 2015.
  7. 1 2 3 4 5 6 7 8 9 "Light Fastness of Textiles: Factors Affecting and Control Measures". Textile Learner. Retrieved 5 March 2015.
  8. "Organic vs Inorganic Pigments". Kolorjet Chemicals Pvt Ltd. Retrieved 6 February 2017.
  9. "Art Glossary: Carbon Black". Kolorjet Chemicals Pvt Ltd. Retrieved 6 February 2017.
  10. 1 2 3 4 "lightfastness tests". Bruce MacEvoy. 2015. Retrieved 6 February 2017.
  11. 1 2 "ASTM D4303 – 10(2016), Standard Test Methods for Lightfastness of Colorants Used in Artists' Materials". American Standard Test Measure International. 2016. Retrieved 6 February 2017.
  12. 1 2 "ISO 105-B01:2014 Textiles – Tests for colour fastness – Part B01: Colour fastness to light: Daylight". International Organization for Standardization. 2014. Retrieved 6 February 2017.
  13. 1 2 "ISO 105-B02:2014, Textiles – Tests for colour fastness – Part B02: Colour fastness to artificial light: Xenon arc fading lamp test". International Organization for Standardization. 2014. Retrieved 6 February 2017.
  14. "ISO 12040:1997, Graphic technology – Prints and printing inks – Assessment of light fastness using filtered xenon arc light". International Organization for Standardization. 1997. Retrieved 6 February 2017.
  15. "Pigments". BASF SE. 2016. Retrieved 6 February 2017.