In metallurgy, a flux (derived from Latin fluxus meaning “flow”) is a chemical cleaning agent, flowing agent, or purifying agent. Fluxes may have more than one function at a time. They are used in both extractive metallurgy and metal joining.
Some of the earliest known fluxes were carbonate of soda, potash, charcoal, coke, borax, lime, lead sulfide and certain minerals containing phosphorus. Iron ore was also used as a flux in the smelting of copper. These agents served various functions, the simplest being a reducing agent, which prevented oxides from forming on the surface of the molten metal, while others absorbed impurities into the slag, which could be scraped off the molten metal. As cleaning agents, fluxes facilitate soldering, brazing, and welding by removing oxidation from the metals to be joined. Common fluxes are: ammonium chloride or rosin for soldering tin; hydrochloric acid and zinc chloride for soldering galvanized iron (and other zinc surfaces); and borax for brazing, braze-welding ferrous metals, and forge welding.
In the process of smelting, inorganic chlorides, fluorides (see fluorite), limestone and other materials are designated as "fluxes" when added to the contents of a smelting furnace or a cupola for the purpose of purging the metal of chemical impurities such as phosphorus, and of rendering slag more liquid at the smelting temperature. The slag is a liquid mixture of ash, flux, and other impurities. This reduction of slag viscosity with temperature, increasing the flow of slag in smelting, is the original origin of the word flux in metallurgy. Fluxes are also used in foundries for removing impurities from molten nonferrous metals such as aluminium, or for adding desirable trace elements such as titanium.
In high-temperature metal joining processes (welding, brazing and soldering), the primary purpose of flux is to prevent oxidation of the base and filler materials. for example, tin-lead solder attaches very well to copper, but poorly to the various oxides of copper, which form quickly at soldering temperatures. Flux is a substance, which is nearly inert at room temperature, but which becomes strongly reducing at elevated temperatures, preventing the formation of metal oxides. Additionally, flux allows solder to flow easily on the working piece rather than forming beads, as it would otherwise.
The role of a flux in joining processes is typically dual: dissolving of the oxides on the metal surface, which facilitates wetting by molten metal, and acting as an oxygen barrier by coating the hot surface, preventing its oxidation. In some applications molten flux also serves as a heat-transfer medium, facilitating heating of the joint by the soldering tool or molten solder.
Fluxes for soft soldering are typically of organic nature, though inorganic fluxes, usually based on halogenides and/or acids, are also used in non-electronics applications. Fluxes for brazing operate at significantly higher temperatures and are therefore mostly inorganic; the organic compounds tend to be of supplementary nature.
Organic fluxes typically consist of four major components:
Inorganic fluxes contain components playing the same role as in organic fluxes. They are more often used in brazing and other high-temperature applications, where organic fluxes have insufficient thermal stability. The chemicals used often simultaneously act as both vehicles and activators; typical examples are borax, borates, fluoroborates, fluorides and chlorides. Halogenides are active at lower temperatures than borates, and are therefore used for brazing of aluminium and magnesium alloys; they are however highly corrosive.
Fluxes have several important properties:
The surface of the tin-based solder is coated predominantly with tin oxides; even in alloys the surface layer tends to become relatively enriched by tin. Fluxes for indium and zinc based solders have different compositions than fluxes for ordinary tin-lead and tin-based solders, due to different soldering temperatures and different chemistry of the oxides involved.
The composition of fluxes is tailored for the required properties - the base metals and their surface preparation (which determine the composition and thickness of surface oxides), the solder (which determines the wetting properties and the soldering temperature), the corrosion resistance and ease of removal, and others.
Organic fluxes are unsuitable for flame soldering and flame brazing, as they tend to char and impair solder flow.
Some metals are classified as "unsolderable" in air, and have to be either coated with another metal before soldering or special fluxes and/or protective atmospheres have to be used. Such metals are beryllium, chromium, magnesium, titanium, and some aluminium alloys.
Fluxes for high-temperature soldering differ from the fluxes for use at lower temperatures. At higher temperatures even relatively mild chemicals have sufficient oxide-disrupting activity, but the metal oxidation rates become fairly high; the barrier function of the vehicle therefore becomes more important than the fluxing activity. High molecular weight hydrocarbons are often used for this application; a diluent with a lower molecular weight, boiling off during the preheat phase, is usually used to aid application.
The role of the activators is primarily disruption and removal of the oxide layer on the metal surface (and also the molten solder), to facilitate direct contact between the molten solder and metal. The reaction product is usually soluble or at least dispersible in the molten vehicle. The activators are usually either acids, or compounds that release acids at elevated temperature.
The general reaction of oxide removal is:
Salts are ionic in nature and can cause problems from metallic leaching or dendrite growth, with possible product failure. In some cases, particularly in high-reliability applications, flux residues must be removed.
The activity of the activator generally increases with temperature, up to a certain value where activity ceases, either due to thermal decomposition or excessive volatilization. However the oxidation rate of the metals also increases with temperature.
At high temperatures, copper oxide reacts with hydrogen chloride to water-soluble and mechanically weak copper chloride, and with rosin to salts of copper and abietic acid which is soluble in molten rosin.
Some activators may also contain metal ions, capable of exchange reaction with the underlying metal; such fluxes aid soldering by chemically depositing a thin layer of easier solderable metal on the exposed base metal. An example is the group of fluxes containing zinc, tin or cadmium compounds, usually chlorides, sometimes fluorides or fluoroborates.
Common high-activity activators are mineral acids, often together with halides, amines, water and/or alcohols:
Inorganic acids are highly corrosive to metals even at room temperature, which causes issues during storage, handling and applications. As soldering involves high temperatures, compounds that decompose or react with acids as products are frequently used:
The terms resin flux and rosin flux are ambiguous and somewhat interchangeable, with different vendors using different assignments. Generally, fluxes are labeled as rosin if the vehicle they are based on is primarily natural rosin. Some manufactures reserve "rosin" designation for military fluxes based on rosin (R, RMA and RA compositions) and label others as "resin".
Rosin has good flux properties. A mixture of organic acids (resin acids, predominantly abietic acid, with pimaric acid, isopimaric acid, neoabietic acid, dihydroabietic acid, and dehydroabietic acid), rosin is a glassy solid, virtually nonreactive and noncorrosive at normal temperature, but liquid, ionic and mildly reactive to metal oxides at molten state. Rosin tends to soften between 60-70 °C and is fully fluid at around 120 °C; molten rosin is weakly acidic and is able to dissolve thinner layers of surface oxides from copper without further additives. For heavier surface contamination or improved process speed, additional activators can be added.
There are three types of rosin: gum rosin (from pine tree oleoresin), wood rosin (obtained by extraction of tree stumps), and tall oil rosin (obtained from tall oil, a byproduct of kraft paper process). Gum rosin has a milder odor and lower tendency to crystallize from solutions than wood rosin, and is therefore preferred for flux applications. Tall oil rosin finds increased use due to its higher thermal stability and therefore lower tendency to form insoluble thermal decomposition residues. The composition and quality of rosin differs by the tree type, and also by location and even by year. In Europe, rosin for fluxes is usually obtained from a specific type of Portuguese pine, in America a North Carolina variant is used.
Natural rosin can be used as-is, or can be chemically modified by e.g. esterification, polymerization, or hydrogenation. The properties being altered are increased thermal stability, better cleanability, altered solution viscosity, and harder residue (or conversely, softer and more tacky residue). Rosin can be also converted to a water-soluble rosin flux, by formation of an ethoxylated rosin amine, an adduct with a polyglycol and an amine.
Fluxes can be also prepared from synthetic resins, often based on esters of polyols and fatty acids. Such resins have improved fume odor and lower residue tack, but their fluxing activity and solubility tend to be lower than of natural resins.
R, WW, and RMA grades are used for joints that can not be easily cleaned or where there is too high corrosion risk. More active grades require thorough cleaning of the residues. Improper cleaning can actually aggravate the corrosion by releasing trapped activators from the flux residues.
There are several possible activator groups for rosins:
Solder fluxes are specified according to several standards.
The most common one in European setting is the ISO 9454-1 (also known as DIN EN 29454-1).
The flux classes according to ISO 9454-1 are specified by four-character code, by flux type, base, activator, and type. The form code is often omitted.
Therefore, 1.1.2 means rosin flux with halides.
The older specification, still often in use for specifying fluxes in shops, is the older German DIN 8511; the pairing is, however, not always one-to-one (note the multiple vs. one relation old standard vs. new standard in table below
|Strongly corrosive||F-SW-11||3.2.2||Inorganic acid other than phosphoric|
|Strongly corrosive||F-SW-12||3.1.1||Ammonium chloride|
|Strongly corrosive||F-SW-13||3.2.1||Phosphoric acid|
|Weakly corrosive||F-SW-21||3.1.1||Ammonium chloride|
|Weakly corrosive||F-SW-22||3.1.2||Inorganic salts without ammonium chloride|
|Weakly corrosive||F-SW-23||2.1.3||Organic water-soluble without halides|
|Weakly corrosive||F-SW-23||2.2.1||Organic water-insoluble without activators|
|Weakly corrosive||F-SW-23||2.2.3||Organic water-insoluble without halides|
|Weakly corrosive||F-SW-24||2.1.1||Organic water-soluble without activators|
|Weakly corrosive||F-SW-24||2.1.3||Organic water-soluble without halides|
|Weakly corrosive||F-SW-24||2.2.3||Organic water-insoluble without halides|
|Weakly corrosive||F-SW-25||2.1.2||Organic water-soluble with halides|
|Weakly corrosive||F-SW-25||2.2.2||Organic water-insoluble with halides|
|Weakly corrosive||F-SW-26||1.1.2||Rosin with halides|
|Weakly corrosive||F-SW-27||1.1.3||Rosin without halides|
|Weakly corrosive||F-SW-28||1.2.2||Rosin-free resin with halides|
|Non-corrosive||F-SW-31||1.1.1||Rosin without activators|
|Non-corrosive||F-SW-32||1.1.3||Rosin without halides|
|Non-corrosive||F-SW-33||1.2.3||Rosin-free resin without halides|
|Non-corrosive||F-SW-34||2.2.3||Organic water-insoluble without halides|
One standard increasing used (United States) is J-STD-004 (very similar to DIN EN 61190-1-1). Four characters (two letters, then one letter, and last a number) represent flux composition, flux activity, and whether activators include halides:
Base RO(sin) - RE(sin) - OR(ganic) - IN(organic)
Activity L(ow) - M(oderate)-H(igh)
Halide content <0.05% 0 (No) - 1 (Yes)
Any combination is possible, e.g. ROL0, REM1 or ORH0.
Some materials are very difficult to solder. In some cases special fluxes have to be employed.
Fluxes have several serious drawbacks:
In special cases the drawbacks are sufficiently serious to warrant using fluxless techniques.
Acid flux types (not used in electronics) may contain hydrochloric acid, zinc chloride or ammonium chloride, which are harmful to humans. Therefore, flux should be handled with gloves and goggles, and used with adequate ventilation.
Prolonged exposure to rosin fumes released during soldering can cause occupational asthma (formerly called colophony disease in this context) in sensitive individuals, although it is not known which component of the fumes causes the problem.
While molten solder has low tendency to adhere to organic materials, molten fluxes, especially of the resin/rosin type, adhere well to fingers. A mass of hot sticky flux can transfer more heat to skin and cause more serious burns than a comparable particle of non-adhering molten metal, which can be quickly shaken off. In this regard, molten flux is similar to molten hot glue.
In some cases the presence of flux is undesirable; flux traces interfere with e.g. precision optics or MEMS assemblies. Flux residues also tend to outgas in vacuum and space applications, and traces of water, ions and organic compounds may adversely affect long-term reliability of non-hermetic packages. Trapped flux residues are also the cause of most voids in the joints. Flux-less techniques are therefore desirable there.
For successful soldering and brazing, the oxide layer has to be removed from both the surfaces of the materials and the surface of the filler metal preform; the exposed surfaces also have to be protected against oxidation during heating. Flux-coated preforms can also be used to eliminate flux residue entirely from the soldering process.
Protection of the surfaces against further oxidation is relatively simple, by using vacuum or inert atmosphere. Removal of the native oxide layer is more troublesome; physical or chemical cleaning methods have to be employed and the surfaces can be protected by e.g. gold plating. The gold layer has to be sufficiently thick and non-porous to provide protection for reasonable storage time. Thick gold metallization also limits choice of soldering alloys, as tin-based solders dissolve gold and form brittle intermetallics, embrittling the joint. Thicker gold coatings are usually limited to use with indium-based solders and solders with high gold content.
Removal of the oxides from the solder preform is also troublesome. Fortunately some alloys are able to dissolve the surface oxides in their bulk when superheated by several degrees above their melting point; the Sn-Cu1 and Sn-Ag4 require superheating by 18-19 °C, the Sn-Sb5 requires as little as 10 °C, but the Sn-Pb37 alloy requires 77 °C above its melting point to dissolve its surface oxide. The self-dissolved oxide however degrades the solder's properties and increases its viscosity in molten state, this approach is therefore not optimal. Solder preforms are preferred to be with high volume-to-surface ratio, as that limits the amount of oxide being formed. Pastes have to contain smooth spherical particles, preforms are ideally made of round wire. The problem with preforms can be also sidestepped by depositing the solder alloy directly on the surfaces of the parts and/or substrates, by e.g. chemical or electrochemical means.
Protective atmosphere with chemically reducing properties can be beneficial in some cases. Molecular hydrogen can be used to reduce surface oxides of tin and indium at temperatures above 430 and 470 °C; for zinc the temperature is above 500 °C, where zinc is already becoming volatilized. (At lower temperatures the reaction speed is too slow for practical applications.) Very low partial pressures of oxygen and water vapor have to be achieved for the reaction to proceed.
Other reactive atmospheres are also in use. Vapors of formic acid and acetic acid are the most commonly used. Carbon monoxide and halogen gases (e.g. carbon tetrafluoride, sulfur hexafluoride, or dichlorodifluoromethane) require fairly high temperatures for several minutes to be effective.
Atomic hydrogen is much more reactive than molecular hydrogen. In contact with surface oxides it forms hydroxides, water, or hydrogenated complexes, which are volatile at soldering temperatures. The most practical dissociation method is probably an electrical discharge. Argon-hydrogen gas compositions with hydrogen concentration below the low flammable limit can be used, eliminating the safety issues. The operation has to be performed at low pressure, as the stability of atomic hydrogen at atmospheric pressure is insufficient. Such hydrogen plasma can be used for fluxless reflow soldering.
Active atmospheres are relatively common in furnace brazing; due to the high process temperatures the reactions are reasonably fast. The active ingredients are usually carbon monoxide (possibly in the form of combusted fuel gas) and hydrogen. Thermal dissociation of ammonia yields an inexpensive mixture of hydrogen and nitrogen.
Bombardment with atomic particle beams can remove surface layers at a rate of tens of nanometers per minute. The addition of hydrogen to the plasma augments the removal efficiency by chemical mechanisms.
Mechanical agitation is another possibility for disrupting the oxide layer. Ultrasound can be used for assisting tinning and soldering; an ultrasonic transducer can be mounted on the soldering iron, in a solder bath, or in the wave for wave soldering. The oxide disruption and removal involves cavitation effects between the molten solder and the base metal surface. A common application of ultrasound fluxing is in tinning of passive parts (active parts do not cope well with the mechanical stresses involved); even aluminium can be tinned this way. The parts can then be soldered or brazed conventionally.
Mechanical rubbing of a heated surface with molten solder can be used for coating the surface. Both surfaces to be joined can be prepared this way, then placed together and reheated. This technique was formerly used to repair small damages on aluminium aircraft skins.
Very thin layer of zinc can be used for joining aluminium parts. The parts have to be perfectly machined, or pressed together, due to the small volume of filler metal. At high temperature applied for long time, the zinc diffuses away from the joint. The resulting joint does not present a mechanical weakness and is corrosion-resistant. The technique is known as diffusion soldering.
Fluxless brazing of copper alloys can be done with self-fluxing filler metals. Such metals contain an element capable of reaction with oxygen, usually phosphorus. A good example is the family of copper-phosphorus alloys.
In soldering of metals, flux serves a threefold purpose: it removes any oxidized metal from the surfaces to be soldered, seals out air thus preventing further oxidation, and by facilitating amalgamation improves wetting characteristics of the liquid solder. Some fluxes are corrosive, so the parts have to be cleaned with a damp sponge or other absorbent material after soldering to prevent damage. Several types of flux are used in electronics.
A number of standards exist to define the various flux types. The principal standard is J-STD-004.
J-STD-004 characterizes the flux by type (e.g. Rosin (RO), Resin (RE), Organic (OR), Inorganic (IN)), its activity (strength of fluxing) and reliability of residue from a surface insulation resistance (SIR) and electromigration standpoint, and whether or not it contains halide activators.
This replaces the old MIL QQS standard which defined fluxes as:
|RMA||(Rosin mildly activated)|
Any of these categories (except WS) may be no-clean, or not, depending on the chemistry selected and the standard that the manufacturer requires.
J-STD-004 includes tests for electromigration and surface insulation resistance (which must be greater than 100 MΩ after 168 hours at elevated temperature and humidity with a DC bias applied).
Brazing (sometimes known as silver soldering or hard soldering) requires a much higher temperature than soft soldering, sometimes over 850 °C. As well as removing existing oxides, rapid oxidation of the metal at the elevated temperatures has to be avoided. This means that fluxes need to be more aggressive and to provide a physical barrier. Traditionally borax was used as a flux for brazing, but there are now many different fluxes available, often using active chemicals such as fluorides as well as wetting agents. Many of these chemicals are toxic and due care should be taken during their use.
A related use of flux is to designate the material added to the contents of a smelting furnace or a cupola for the purpose of purging the metal of impurities, and of rendering the slag more liquid. The flux most commonly used in iron and steel furnaces is limestone, which is charged in the proper proportions with the iron and fuel. The slag is a liquid mixture of ash, flux, and other impurities.
Hot corrosion can affect gas turbines operating in high salt environments (e.g., near the ocean). Salts, including chlorides and sulfates, are ingested by the turbines and deposited in the hot sections of the engine; other elements present in fuels also form salts, e.g. vanadates. The heat from the engine melts these salts which then can flux the passivating oxide layers on the metal components of the engine, allowing corrosion to occur at an accelerated rate.
|Wikisource has the text of the 1911 Encyclopædia Britannica article Flux.|