Dealkalization is a process of surface modification applicable to glasses containing alkali ions, wherein a thin surface layer is created that has a lower concentration of alkali ions than is present in the underlying, bulk glass. This change in surface composition commonly alters the observed properties of the surface, most notably enhancing corrosion resistance.
Many commercial glass products such as containers are made of soda-lime glass, and therefore have a substantial percentage of sodium ions in their internal structure. Since sodium is an alkali element, its selective removal from the surface results in a dealkalized surface. A classic example of dealkalization is the treatment of glass containers, where a special process is used to create a dealkalized inside surface that is more resistant to interactions with liquid products put inside the container. However, the term dealkalization may also be generally applied to any process where a glass surface forms a thin surface layer that is depleted of alkali ions relative to the bulk. A common example is the initial stages of glass corrosion or weathering, where alkali ions are leached from the surface region by interactions with water, forming a dealkalized surface layer.
A dealkalized surface may have either no alkali remaining or may just have less than the bulk. In silicate glasses, dealkalized surfaces are also often considered "silica-rich" since the selective removal of alkali ions can be thought to leave behind a surface composed primarily of silica (SiO2). To be precise, dealkalization does not generally involve the outright removal of alkali from the glass, but rather its replacement with protons (H+) or hydronium ions (H3O+) in the structure through the process of ion-exchange.
For glass containers, the goal of surface dealkalization is to render the inside surface of the container more resistant to interactions with liquid products later put inside it. Since the treatment is directed primarily at changing the properties of the inside surface in contact with the product, it is also referred to as "internal treatment".
The most common example of its use with containers is on bottles intended to hold alcoholic spirits. The reason for this is that some alcoholic spirits such as vodka and gin have an approximately neutral pH and a high alcohol content, but are not buffered in any way against changes in pH. If alkali is leached from the glass into the product, the pH will begin to rise (i.e. become more alkaline), can eventually reach a pH high enough that the solution begins to attack the glass itself quite effectively. [1] [2] By this mechanism, initially neutral alcohol products can achieve a pH where the glass container itself begins to slowly dissolve, leaving thin, siliceous glass flakes or particles in the fluid. Dealkalization treatment hinders this process by removing alkali from the inside surface. Not only does this mean less extractable alkali in the glass surface directly contacting the product, but it also creates a barrier for the diffusion of alkali from the underlying bulk glass into the product. [3]
The same logic applies in pharmaceutical glass items such as vials that are intended to hold medicinal products. While many of these items are composed of more durable borosilicate glass, they are also at times dealkalized in order to minimize the possibility of alkali leaching from the glass into the product. This action helps to avoid undesired changes in pH or ionic strength of the solution, which not only inhibits eventual attack of the glass as previously described, but can also be important in maintaining the efficacy or stability of sensitive product formulations.
Dealkalizing glass containers is accomplished by exposing the glass surface to reactive sulfur- or fluorine-containing compounds during the manufacturing process. A rapid ion-exchange reaction proceeds that depletes the inside surface of alkali, and is performed when the glass is at high temperature, usually on the order of 500–650 °C or greater. [4]
Historically, sulfur-containing compounds were the first materials used to dealkalize glass containers. Dealkalization proceeds through the interdiffusion/ion-exchange of Na+ out of the glass and H+/H3O+ into the glass, along with the subsequent reaction of the sulfate species with available sodium at the surface to form sodium sulfate (Na2SO4). The latter is left behind as water-soluble crystalline deposits, or bloom, on the glass surface that must be rinsed away prior to filling. On manufacturing lines, one way in which this process was done was by flooding the annealing lehr with sulfur dioxide (SO2) or sulfur trioxide (SO3) gases—especially in the presence of water, which enhances the reaction. However, this practice fell into disfavor due to environmental and health concerns regarding SOx-type gases. [5] An alternative method for sulfate treatment is with solid ammonium sulfate salt or aqueous solutions thereof. These materials are introduced inside the container after forming and decompose into gases in the annealing lehr, where the resulting sulfur-containing gas mixture carries out the dealkalization reaction. This method is purportedly safer than flooding the annealing lehr since the unreacted components in the gas mixture will tend not to escape to the atmosphere, but rather react with each other and recreate the original salt in the container that can later be rinsed away. [6]
Treatment with fluorine-containing compounds is typically accomplished through the injection of a fluorinated gas mixture (e.g. 1,1-difluoroethane mixed with air) into bottles at high temperatures. The gas can be delivered to the container either in the air used in the forming process (i.e. during the final blow of the container into its desired shape), or with a nozzle directing a stream of the gas down into the mouth of the bottle as it passes on a conveyor belt after forming but before annealing. The mixture gently combusts inside the bottle, creating an extremely small dose of hydrofluoric acid that reacts with the glass surface and serves to dealkalize it. The resultant surface is virtually free from any residues of the process. [7] This treatment is also known as the Ball I.T. process (I.T. standing for internal treatment) as Ball Corporation held the patent and developed the first commercially available system implementing this process.
Routine tests for surface dealkalization in the glass container industry all generally aim to evaluate the amount of alkali extracted from the glass when it is rinsed with or exposed to purified water. For example, dealkalization can be quickly checked by introducing a small volume of distilled water to a freshly made bottle and rolling the bottle gently to pass the water completely over its inside surface. The pH of the rinse water is then measured; untreated containers will tend to yield a slightly alkaline pH in the 8-9 range due to extracted alkali, while dealkalized containers tend to yield a pH that remains approximately neutral.
A much more thorough version of this test is outlined in various international and domestic testing standards for glass containers, [8] [9] [10] all with comparable methodologies. These tests evaluate the hydrolytic stability of the containers under more severe conditions, wherein containers, filled close to capacity with purified water, are covered and then heat-cycled in an autoclave at 121 °C for 1 hour. After cooling to room temperature, the water is titrated with acid to evaluate the pH of the water, and therefore the equivalent amount of alkali extracted during the heat cycle. The alkali content of the rinse water can also be evaluated more directly by chemical analysis of the rinse water, as outlined in more recent versions of the European Pharmacopoeia. According to the Pharmacopoeia standards, internally treated or dealkalized soda-lime glass containers are designated as "Type II" containers, thus setting them apart from their untreated counterparts due to their improved resistance to product interactions (as opposed to "Type III", which is standard, untreated soda-lime glass, or "Type I", which is reserved for highly resistant borosilicate glass).
While not routine, dealkalization can also be measured in a variety of other ways. Since dealkalized surfaces are more chemically durable, they are also more resistant to weathering reactions, and appropriate evaluation of this parameter can give indirect evidence of a previously dealkalized surface. It is also possible to evaluate dealkalization through the use of advanced, surface analytical techniques such as SIMS or XPS, which give direct measurements of glass surface composition. [11] [12]
Sulfuric acid (alternative spelling sulphuric acid), also known as vitriol, is a mineral acid composed of the elements sulfur, oxygen and hydrogen, with molecular formula H2SO4. It is a colorless, odorless, and syrupy liquid that is soluble in water and is synthesized in reactions that are highly exothermic.
Brine is a high-concentration solution of salt in water. In different contexts, brine may refer to salt solutions ranging from about 3.5% up to about 26%. Lower levels of concentration are called by different names: fresh water, brackish water, and saline water.
Hydrogen sulfide is the chemical compound with the formula H
2S. It is a colorless chalcogen hydride gas with the characteristic foul odor of rotten eggs. It is very poisonous, corrosive, and flammable.
Corrosion is a natural process that converts a refined metal into a more chemically-stable form such as oxide, hydroxide, or sulfide. It is the gradual destruction of materials by chemical and/or electrochemical reaction with their environment. Corrosion engineering is the field dedicated to controlling and preventing corrosion.
Sodium carbonate, Na2CO3, (also known as washing soda, soda ash and soda crystals) is the inorganic compound with the formula Na2CO3 and its various hydrates. All forms are white, water-soluble salts. All forms have a strongly alkaline taste and give moderately alkaline solutions in water. Historically it was extracted from the ashes of plants growing in sodium-rich soils. Because the ashes of these sodium-rich plants were noticeably different from ashes of wood (once used to produce potash), sodium carbonate became known as "soda ash". It is produced in large quantities from sodium chloride and limestone by the Solvay process.
The lead–acid battery was invented in 1859 by French physicist Gaston Planté and is the earliest, yet still most widely used, type of rechargeable battery. Despite having a very low energy-to-weight ratio and a low energy-to-volume ratio, its ability to supply high surge currents means that the cells have a relatively large power-to-weight ratio. These features, along with their low cost, make them attractive for use in motor vehicles to provide the high current required by automobile starter motors.
A corrosive substance is one that will damage or destroy other substances with which it comes into contact by means of a chemical reaction.
Calcium sulfate (or calcium sulphate) is the inorganic compound with the formula CaSO4 and related hydrates. In the form of γ-anhydrite (the anhydrous form), it is used as a desiccant. One particular hydrate is better known as plaster of Paris, and another occurs naturally as the mineral gypsum. It has many uses in industry. All forms are white solids that are poorly soluble in water. Calcium sulfate causes permanent hardness in water.
The Leblanc process was an early industrial process for the production of soda ash used throughout the 19th century, named after its inventor, Nicolas Leblanc. It involved two stages: production of sodium sulfate from sodium chloride, followed by reaction of the sodium sulfate with coal and calcium carbonate to produce sodium carbonate. The process gradually became obsolete after the development of the Solvay process.
Plating is a surface covering in which a metal is deposited on a conductive surface. Plating has been done for hundreds of years; it is also critical for modern technology. Plating is used to decorate objects, for corrosion inhibition, to improve solderability, to harden, to improve wearability, to reduce friction, to improve paint adhesion, to alter conductivity, to improve IR reflectivity, for radiation shielding, and for other purposes. Jewelry typically uses plating to give a silver or gold finish.
Sodium sulfite (sodium sulphite) is a soluble sodium salt of sulfurous acid (sulfite) with the chemical formula Na2SO3. It is used as a preservative to prevent dried fruit from discoloring, and for preserving meats, and is used in the same way as sodium thiosulfate to convert elemental halogens to their respective hydrohalic acids, in photography and for reducing chlorine levels in pools. In boiler systems, sulfite and bisulfite are the most commonly employed oxygen scavengers used to prevent pitting corrosion. Sodium sulfite is also a byproduct of sulfur dioxide scrubbing, a part of the flue-gas desulfurization process.
Ion exchange is an exchange of ions between two electrolytes or between an electrolyte solution and a complex. In most cases the term is used to denote the processes of purification, separation, and decontamination of aqueous and other ion-containing solutions with solid polymeric or mineralic "ion exchangers".
Stress corrosion cracking (SCC) is the growth of crack formation in a corrosive environment. It can lead to unexpected sudden failure of normally ductile metal alloys subjected to a tensile stress, especially at elevated temperature. SCC is highly chemically specific in that certain alloys are likely to undergo SCC only when exposed to a small number of chemical environments. The chemical environment that causes SCC for a given alloy is often one which is only mildly corrosive to the metal. Hence, metal parts with severe SCC can appear bright and shiny, while being filled with microscopic cracks. This factor makes it common for SCC to go undetected prior to failure. SCC often progresses rapidly, and is more common among alloys than pure metals. The specific environment is of crucial importance, and only very small concentrations of certain highly active chemicals are needed to produce catastrophic cracking, often leading to devastating and unexpected failure.
Boiler water is liquid water within a boiler, or in associated piping, pumps and other equipment, that is intended for evaporation into steam. The term may also be applied to raw water intended for use in boilers, treated boiler feedwater, steam condensate being returned to a boiler, or boiler blowdown being removed from a boiler.
Phosphate coatings are used on steel parts for corrosion resistance, lubricity, or as a foundation for subsequent coatings or painting. It serves as a conversion coating in which a dilute solution of phosphoric acid and phosphate salts is applied via spraying or immersion and chemically reacts with the surface of the part being coated to form a layer of insoluble, crystalline phosphates. Phosphate conversion coatings can also be used on aluminium, zinc, cadmium, silver and tin.
Biogenic sulfide corrosion is a bacterially mediated process of forming hydrogen sulfide gas and the subsequent conversion to sulfuric acid that attacks concrete and steel within wastewater environments. The hydrogen sulfide gas is biochemically oxidized in the presence of moisture to form sulfuric acid. The effect of sulfuric acid on concrete and steel surfaces exposed to severe wastewater environments can be devastating. In the USA alone, corrosion is causing sewer asset losses estimated at around $14 billion per year. This cost is expected to increase as the aging infrastructure continues to fail.
Glass production involves two main methods – the float glass process that produces sheet glass, and glassblowing that produces bottles and other containers.
Concrete degradation may have various causes. Concrete can be damaged by fire, aggregate expansion, sea water effects, bacterial corrosion, calcium leaching, physical damage and chemical damage. This process adversely affects concrete exposed to these damaging stimuli.
Plasma-activated bonding is a derivative, directed to lower processing temperatures for direct bonding with hydrophilic surfaces. The main requirements for lowering temperatures of direct bonding are the use of materials melting at low temperatures and with different coefficients of thermal expansion (CTE).
Mixed oxidant solution is a kind of Disinfection which is used for disinfecting, sterilization and eliminating pathogenic microorganisms in water and in many other applications. Using Mixed oxidant solution for water disinfection, compared to other methods, such as sodium hypochlorite, Calcium hypochlorite, chlorine gas and ozonation has various benefits such as higher disinfecting power, stable residual chlorine in water, improved taste and odor, elimination of biofilm and safety. Mixed oxidant solution is produced from electrolysis of sodium chloride brine (sodium chloride) and it's a mixture of disinfecting compounds. The main component of this product is chlorine and its derivatives (ClO−, HClO and Cl2 solution). It also contains high amounts of chlorine dioxide (ClO2) solution, dissolved ozone, hydrogen peroxide(H2O2) and oxygen. This is the reason for calling this solution mixed oxidant.