Boric acid

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Orthoboric acid
Structural formula
Structural formula
Space-filling model
Space-filling model
Boric acid crystals
Names
IUPAC name
Boric acid[1]
Other names
Orthoboric acid, Boracic acid, Sassolite, Borofax, Trihydroxyborane, Boranetriol, Hydrogen borate, Acidum boricum
Identifiers
3D model (
JSmol
)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
 100.030.114 Edit this at Wikidata
EC Number
  • 233-139-2
E number E284 (preservatives)
KEGG
UNII
  • InChI=1S/BH3O3/c2-1(3)4/h2-4H checkY
    Key: KGBXLFKZBHKPEV-UHFFFAOYSA-N checkY
  • InChI=1/BH3O3/c2-1(3)4/h2-4H
    Key: KGBXLFKZBHKPEV-UHFFFAOYAI
  • OB(O)O
  • [OH+]=[B-](O)O
Properties
BH3O3
Molar mass 61.83 g·mol−1
Appearance White crystalline solid
Density 1.435 g/cm3
Melting point 170.9 °C (339.6 °F; 444.0 K)
Boiling point 300 °C (572 °F; 573 K)
2.52 g/100 mL (0 °C)
4.72 g/100 mL (20 °C)
5.7 g/100 mL (25 °C)
19.10 g/100 mL (80 °C)
27.53 g/100 mL (100 °C)
Solubility in other solvents Soluble in lower alcohols
moderately soluble in pyridine
very slightly soluble in acetone
log P -0.29[2]
Acidity (pKa) 9.24 (first proton), 12.4 (second), 13.3 (complete)
Conjugate base
 Borate
-34.1·10−6 cm3/mol
Structure
Trigonal planar
0 D
Pharmacology
S02AA03 (WHO) D08AD (WHO)
Hazards
GHS labelling:
GHS08: Health hazard
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Flash point Nonflammable
Lethal dose or concentration (LD, LC):
2660 mg/kg, oral (rat)
Related compounds
Related compounds
 Boron trioxide
Borax
Supplementary data page
Boric acid (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Boric acid, more specifically orthoboric acid, is a compound of

borate esters
.

Boric acid is often used as an

neutron absorber
, or precursor to other boron compounds.

The term "boric acid" is also used generically for any

oxoacid of boron, such as metaboric acid HBO2 and tetraboric acid
H2B4O7.

History

Orthoboric acid was first prepared by Wilhelm Homberg (1652–1715) from borax, by the action of mineral acids, and was given the name sal sedativum Hombergi ("sedative salt of Homberg"). However boric acid and borates have been used since the time of the ancient Greeks for cleaning, preserving food, and other activities.[4]

Molecular and crystal structure

The three oxygen atoms form a trigonal planar geometry around the boron. The B-O bond length is 136 pm and the O-H is 97 pm. The molecular point group is C3h.[5]

Two crystalline forms of orthoboric acid are known:

hexagonal. The former is the most common; the second, which is a bit more stable thermodynamically, can be obtained with a special preparation method.[6]

Triclinic

The triclinic form of boric acid consists of layers of B(OH)3 molecules held together by hydrogen bonds with an O...O separation of 272 pm. The distance between two adjacent layers is 318 pm.[7]

The unit cell of boric acid
hydrogen bonding (dashed lines)
allows boric acid molecules to form
parallel layers in the solid state

Preparation

Boric acid may be prepared by reacting borax (sodium tetraborate decahydrate) with a mineral acid, such as hydrochloric acid:

Na2B4O7·10H2O + 2 HCl → 4 B(OH)3 + 2 NaCl + 5 H2O

It is also formed as a by product of hydrolysis of boron trihalides and diborane:[8]

B2H6 + 6 H2O → 2 B(OH)3 + 6 H2
BX3 + 3 H2O → B(OH)3 + 3 HX (X = Cl, Br, I)

Reactions

Pyrolysis

When heated, orthoboric acid undergoes a three step dehydration. The reported transition temperatures vary substantially from source to source.[citation needed]

When heated above 140 °C, orthoboric acid yields metaboric acid (HBO2) with loss of one water molecule:[9][10]

B(OH)3 → HBO2 + H2O

Heating metaboric acid above about 180 °C eliminates another water molecule forming tetraboric acid, also called pyroboric acid (H2B4O7):[9][10]

4 HBO2 → H2B4O7 + H2O

Further heating (to about 530 °C) leads to boron trioxide:[11][9][10]

H2B4O7 → 2 B2O3 + H2O

Aqueous solution

When orthoboric acid is dissolved in water, it partially dissociates to give metaboric acid:

B(OH)3 ⇌ HBO2 + H2O

The solution is mildly acidic due to ionization of the acids:

B(OH)3 + H2O ⇌ [BO(OH)2]− + H3O+
HBO2 + H2O ⇌ [BO2]− + H3O+

However, Raman spectroscopy of strongly alkaline solutions has shown the presence of [B(OH)4]− ions,[12] leading some to conclude that the acidity is exclusively due to the abstraction of OH− from water:[12]

B(OH)3 + HO− ⇌ B(OH)−4

Equivalently,

B(OH)3 + H2O ⇌ B(OH)−4 +  H+ (K = 7.3×10−10; pK = 9.14)

Or, more properly,

B(OH)3 + 2 H2O ⇌ B(OH)−4 + H3O+

This reaction occurs in two steps, with the neutral complex aquatrihydroxyboron B(OH)3(OH2) as an intermediate:[13]

  1. B(OH)3 + H2O → B(OH)3(OH2)
  2. B(OH)3(OH2) + H2O + HO− → [B(OH)4]− + H3O+

This reaction may be characterized as

Brønsted acidity.[14][15][16]
However, some of its behaviour towards some chemical reactions suggest it to be tribasic acid in the Brønsted sense as well.

Boric acid, mixed with borax Na2B4O7·10H2O (more properly Na2B4O5(OH)4·8H2O) in the weight ratio of 4:5, is highly soluble in water, though they are not so soluble separately.[17]

Sulfuric acid solution

Boric acid also dissolves in anhydrous sulfuric acid according to the equation:[7]

B(OH)3 + 6 H2SO4 → [B(SO4H)4]− + 2 [HSO4]− + 3 H3O+

The product is an extremely strong acid, even stronger than the original oleum.[7]

Esterification

Boric acid reacts with alcohols to form

aryl. The reaction is typically driven by a dehydrating agent, such as concentrated sulfuric acid:[18]

B(OH)3 + 3 ROH → B(OR)3 + 3 H2O

With vicinal diols

The acidity of boric acid solutions is greatly increased in the presence of

hydroxyl groups in adjacent carbon atoms, (R1,R2)=C(OH)−C(OH)=(R3,R4)) such as glycerol and mannitol.[19][7][20]

The tetrahydroxyborate anion formed in the dissolution spontaneously reacts with these diols to form relatively stable anion esters containing one or two five-member −B−O−C−C−O− rings. For example, the reaction with mannitol H(HCOH)6H, whose two middle hydroxyls are in cis orientation, can be written as

B(OH)3 + H2O ⇌ [B(OH)4]− + H+
[B(OH)4]− + H(HCOH)6H ⇌ [B(OH)2(H(HCOH)2(HCO−)2(HCOH)2H)]− + 2 H2O
[B(OH)2(H(HCOH)2(HCO−)2(HCOH)2H)]− + H(HCOH)6H ⇌ [B(H(HCOH)2(HCO−)2(HCOH)2H)2]− + 2 H2O

Giving the overall reaction

B(OH)3 + 2 H(HCOH)6H ⇌ [B(H(HCOH)2(HCO−)2(HCOH)2H)2]− + 3 H2O + H+

The stability of these

mannitoboric acid
.

The addition of mannitol to an initially neutral solution containing boric acid or simple borates lowers its

titrator. This property is used in analytical chemistry to determine the borate content of aqueous solutions, for example to monitor the depletion of boric acid by neutrons in the water of the primary circuit of light-water reactor when the compound is added as a neutron poison during refueling operations.[7]

Toxicology

Based on mammalian median lethal dose (LD50) rating of 2,660 mg/kg body mass, boric acid is only poisonous if taken internally or inhaled in large quantities. The Fourteenth Edition of the Merck Index indicates that the LD50 of boric acid is 5.14 g/kg for oral dosages given to rats, and that 5 to 20 g/kg has produced death in adult humans. For a 70 kg adult, at the lower 5 g/kg limit, 350 g could produce death in humans. For comparison's sake, the LD50 of salt is reported to be 3.75 g/kg in rats according to the Merck Index. According to the Agency for Toxic Substances and Disease Registry, "The minimal lethal dose of ingested boron (as boric acid) was reported to be 2–3 g in infants, 5–6 g in children, and 15–20 g in adults. [...] However, a review of 784 human poisonings with boric acid (10–88 g) reported no fatalities, with 88% of cases being asymptomatic."[21]

Long-term exposure to boric acid may be of more concern, causing kidney damage and eventually kidney failure (see links below). Although it does not appear to be

carcinogenic, studies in dogs have reported testicular atrophy after exposure to 32 mg/(kg⋅day) for 90 days. This level, were it applicable to humans at like dose, would equate to a cumulative dose of 202 g over 90 days for a 70 kg adult, not far lower than the above LD50.[22]

According to the CLH report for boric acid published by the Bureau for Chemical Substances Lodz, Poland, boric acid in high doses shows significant developmental toxicity and

risk phrases R60 (may impair fertility) and R61 (may cause harm to the unborn child).[24][25][26][27][28]

At a 2010 European Diagnostics Manufacturing Association (EDMA) Meeting, several new additions to the substance of very high concern (SVHC) candidate list in relation to the Registration, Evaluation, Authorisation and Restriction of Chemicals Regulations 2007 (REACH) were discussed. Following the registration and review completed as part of REACH, the classification of boric acid CAS 10043-35-3 / 11113-50-1 is listed from 1 December 2010 is H360FD (May damage fertility. May damage the unborn child).[29][30]

Uses

Industrial

The primary industrial use of boric acid is in the manufacture of monofilament fiberglass usually referred to as textile fiberglass. Textile fiberglass is used to reinforce plastics in applications that range from boats, to industrial piping to computer circuit boards.[31]

Boric Acid is used as a Nuclear Poison in modern PWR type Nuclear Reactors as it Reduce Fission Process by Reducing Neutrons Flux. It is used in PWR Nuclear Reactor's Coolant water for Controlling Reactor Power as well as to Perform Emergency Reactor Shutdown.

In the jewelry industry, boric acid is often used in combination with

annealing and soldering operations.[citation needed
]

Boric acid is used in the production of the glass in

flat panel displays.[citation needed
]

In

sodium lauryl sulfate and a small portion of H
2SO
4
.

The solution of orthoboric acid and borax in 4:5 ratio is used as a fire retarding agent of wood by impregnation.[32]

It is also used in the manufacturing of

silica-containing powder used for producing induction furnace linings and ceramics
.

Boric acid is added to borax for use as welding flux by blacksmiths.[33]

Boric acid, in combination with polyvinyl alcohol (PVA) or silicone oil, is used to manufacture Silly Putty.[34]

Boric acid is also present in the list of chemical additives used for

propping agents aimed at maintaining the cracks in the shales sufficiently open to facilitate the gas extraction after the hydraulic pressure is relieved.[36][37][38] The rheological properties of borate cross-linked guar gum hydrogel mainly depend on the pH value.[39]

Boric acid is used in some expulsion-type electrical fuses as a de-ionization/extinguishing agent.[40] During an electrical fault in an expulsion-type fuse, a plasma arc is generated by the disintegration and rapid spring-loaded separation of the fusible element, which is typically a specialized metal rod that passes through a compressed mass of boric acid within the fuse assembly. The high-temperature plasma causes the boric acid to rapidly decompose into water vapor and boric anhydride, and in-turn, the vaporization products de-ionize the plasma, helping to interrupt the electrical fault.[41]

Medical

Boric acid can be used as an

vulvovaginal candidiasis.[45][46][47]

As an

antibacterial compound, boric acid can also be used as an acne treatment. It is also used as prevention of athlete's foot, by inserting powder in the socks or stockings. Various preparations can be used to treat some kinds of otitis externa (ear infection) in both humans and animals.[48] The preservative in urine sample bottles in the UK is boric acid.[49]

Boric acid solutions used as an eye wash or on abraded skin are known to be toxic, particularly to infants, especially after repeated use; this is because of its slow elimination rate.[50]

Boric acid is one of the most commonly used substances that can counteract the harmful effects of reactive hydrofluoric acid (HF) after an accidental contact with the skin. It works by forcing the free F− anions into the inert tetrafluoroborate anion. This process defeats the extreme toxicity of hydrofluoric acid, particularly its ability to sequester ionic calcium from blood serum which can lead to cardiac arrest and bone decomposition; such an event can occur from just minor skin contact with HF.[51][failed verification]

Insecticidal

Boric acid was first registered in the US as an insecticide in 1948 for control of

cannibalistic, eat others killed by contact or consumption of boric acid, consuming the powder trapped in the dead roach and killing them, too.[citation needed
]

Preservation

In combination with its use as an insecticide, boric acid also prevents and destroys existing wet and dry rot in timbers. It can be used in combination with an ethylene glycol carrier to treat external wood against fungal and insect attack. It is possible to buy borate-impregnated rods for insertion into wood via drill holes where dampness and moisture is known to collect and sit. It is available in a gel form and injectable paste form for treating rot affected wood without the need to replace the timber. Concentrates of borate-based treatments can be used to prevent slime, mycelium, and algae growth, even in marine environments.[citation needed]

Boric acid is added to salt in the curing of cattle hides, calfskins, and sheepskins. This helps to control bacterial development, and helps to control insects.[citation needed]

pH buffer

Distribution between boric acid and borate ion versus pH assuming pKa = 9.0 (e.g. salt-water swimming pool)
Boric acid predominates in solution below pH 9
Buffer capacity of the boric acid - borate system versus pH assuming pKa = 9.0 (e.g. salt-water swimming pool)
Boric acid buffers against rising pH in swimming pools

Boric acid in equilibrium with its conjugate base the borate ion is widely used (in the concentration range 50–100 ppm boron equivalents) as a primary or adjunct pH buffer system in

Buffer capacity is greater against rising pH (towards the pKa around 9.0), as illustrated in the accompanying graph. The use of boric acid in this concentration range does not allow any reduction in free HOCl concentration needed for pool sanitation, but it may add marginally to the photo-protective effects of cyanuric acid and confer other benefits through anti-corrosive activity or perceived water softness, depending on overall pool solute composition.[55]

Lubrication

Colloidal suspensions of nanoparticles of boric acid dissolved in petroleum or vegetable oil can form a remarkable lubricant on ceramic or metal surfaces[56] with a coefficient of sliding friction that decreases with increasing pressure to a value ranging from 0.10 to 0.02. Self-lubricating B(OH)3 films result from a spontaneous chemical reaction between water molecules and B2O3 coatings in a humid environment. In bulk-scale, an inverse relationship exists between friction coefficient and Hertzian contact pressure induced by applied load.[citation needed]

Boric acid is used to lubricate carrom and novuss boards, allowing for faster play.[57]

Nuclear power

Boric acid is used in some

thermal neutrons. Fission chain reactions are generally driven by the probability that free neutrons will result in fission and is determined by the material and geometric properties of the reactor. Natural boron consists of approximately 20% boron-10 and 80% boron-11 isotopes. Boron-10 has a high cross-section for absorption of low energy (thermal) neutrons. By increasing boric acid concentration in the reactor coolant, the probability that a neutron will cause fission is reduced. Changes in boric acid concentration can effectively regulate the rate of fission taking place in the reactor. During normal at power operation, boric acid is used only in pressurized water reactors (PWRs), whereas boiling water reactors (BWRs) employ control rod pattern and coolant flow for power control, although BWRs can use an aqueous solution of boric acid and borax or sodium pentaborate for an emergency shutdown system if the control rods fail to insert. Boric acid may be dissolved in spent fuel pools used to store spent fuel elements. The concentration is high enough to keep neutron multiplication at a minimum. Boric acid was dumped over Reactor 4 of the Chernobyl nuclear power plant after its meltdown to prevent another reaction from occurring.[citation needed
]

Pyrotechnics

Boron is used in pyrotechnics to prevent the amide-forming reaction between aluminium and nitrates. A small amount of boric acid is added to the composition to neutralize alkaline amides that can react with the aluminium.

Boric acid can be used as a colorant to make fire green. For example, when dissolved in methanol it is popularly used by fire jugglers and fire spinners to create a deep green flame much stronger than copper sulfate.[58]

Agriculture

Boric acid is used to treat or prevent boron deficiencies in plants. It is also used in preservation of grains such as rice and wheat.[59]

References

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Further reading

External links
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