Boric acid salts

Halogenated compounds such as bis(alkyl ether)tetrabromobisphenol A or decabromodiphenyl oxide (DECA) may be used as flame-retardants for polyolefin foams, eventually using antimony oxide, metal oxides, boric acid salts, and metal hydroxides as synergist.92 For example Weil and Levchik93 reported that using suitable amounts of DECA and Sb203, polyethylene foams rated UL94 HF-1 are obtained. 

An improvement over this earlier system was attained with the addition of boron compounds such as boric acid or borate salts [106-108], It has been hypothesized that boric acid and calcium form intramolecular bonds which effectively crosslink or staple an enzyme molecule together [107,108], The use of polyols such as propylene glycol, glycerol, and sorbitol in conjunction with the boric acid salts further enhances the stability of these enzymes [109-111], The patent literature contains numerous examples of enzyme stabilization systems that utilize borates, polyols, carboxylate salts, calcium, and ethanolamines, or combinations thereof [91,112-115],... 

Lehmann, H. A. Recent chemistry of boric acids salts. Z. Chem. 3, 284 (1963). 

Lithium perfluorinated boric acid salt cluster... 

LiTFSA) and lithium bis(pentafluoroethylsulfonyl) amide (LiBETA), lithium fluoroalkylfluorophosphate, lithium bis(oxalate) borate, and lithium perfluorinated boric acid salt cluster. These compounds are currently imder evaluation for commercialization. Lithium bis(oxalate) borate in particular is considered promising as it is a low-cost material containing no fluorine and made from abimdantly available boric acid and oxalic acid. 

A wide variety of corrosion-inhibitor formulations use an alkanolamine as one component. Coolant systems and lubricating oils make use of alkanolamines to protect steel parts from corrosion. The triethanolamine and triisopro-panolamine are used in these formulations as the amine or as an amine soap. The alkanolamine soaps are equivalent or superior to sodium nitrite anticorrosion formulations. A monoisopropanolamine-boric acid salt also has been shown to be superior to sodium nitrite for corrosion protection. 

Synthesis of H2LIO4 cannot, however, be carried out in the presence of K+, Mg +, Zn +, Cd + or Pd " " ions, or in the presence of boric acid salts. Hexaazatetradecine systems [M(L106)j have been obtained from the o-halogen-o -amino derivative L105 on nickel(II) and palladium(II) matrices (Eq. 2.62) [143]. 

Reaction with sodium borohydride. Untreated and Fe-TAML/H202 treated effluents (100 mL) were diluted tenfold with water. NaBH4 (200 mg) was added and stirred at room temperature. Further portions of sodium borohydride (200 mg) were added after two and four days. On day seven, samples (7 mL) were neutralised with 5 % sulfuric acid (2 drops) and centrifuged (3000 rpm, 15 min) to remove boric acid salts before spectral analysis. 

With sodium hydroxide as the base boron of the alkylborane is converted to the water soluble and easily removed sodium salt of boric acid... 

Alkali metals Moisture, acetylene, metal halides, ammonium salts, oxygen and oxidizing agents, halogens, carbon tetrachloride, carbon, carbon dioxide, carbon disul-flde, chloroform, chlorinated hydrocarbons, ethylene oxide, boric acid, sulfur, tellurium... 

An aqueous PVA solution containing a small amount of boric acid may be extmded into an aqueous alkaline salt solution to form a gel-like fiber (15,16). In this process, sodium hydroxide penetrates rapidly into the aqueous PVA solution extmded through orifices to make it alkaline, whereby boric acid cross-links PVA molecules with each other. The resulting fiber is provided with sufficient strength to withstand transportation to the next process step and its cross section does not show a distinct skin/core stmcture. 

Nondurable Finishes. Flame-retardant finishes that are not durable to launderiag and bleaching are, ia general, relatively iaexpensive and efficient (23). In some cases, a mixture of two or more salts is more effective than either of the components alone. For example, an add-on of 60% borax (sodium tetraborate) is required to prevent fabric from burning, and boric acid is iaeffective as a flame retardant even at levels equal to the weight of the fabric. However, a mixture of seven parts borax and three parts boric acid imparts flame resistance to a fabric with as Utde as 6.5% add-on. 

Aqueous mineral acids react with BF to yield the hydrates of BF or the hydroxyfluoroboric acids, fluoroboric acid, or boric acid. Solution in aqueous alkali gives the soluble salts of the hydroxyfluoroboric acids, fluoroboric acids, or boric acid. Boron trifluoride, slightly soluble in many organic solvents including saturated hydrocarbons (qv), halogenated hydrocarbons, and aromatic compounds, easily polymerizes unsaturated compounds such as butylenes (qv), styrene (qv), or vinyl esters, as well as easily cleaved cycHc molecules such as tetrahydrofuran (see Furan derivatives). Other molecules containing electron-donating atoms such as O, S, N, P, etc, eg, alcohols, acids, amines, phosphines, and ethers, may dissolve BF to produce soluble adducts. 

Manufacture. Fluoroborate salts are prepared commercially by several different combinations of boric acid and 70% hydrofluoric acid with oxides, hydroxides, carbonates, bicarbonates, fluorides, and bifluorides. Fluoroborate salts are substantially less corrosive than fluoroboric acid but the possible presence of HF or free fluorides cannot be overlooked. Glass vessels and equipment should not be used. 

Lithium Borates. Lithium metaborate [13453-69-5], LLBO2 2H20, is prepared from reaction of lithium hydroxide and boric acid. It is used as the fluxing agent for the matrix for x-ray fluorescence analytical techniques and in specialty glasses and enamels. The anhydrous salt melts at 847°C. 

The tertiary metal phosphates are of the general formula MPO where M is B, Al, Ga, Fe, Mn, etc. The metal—oxygen bonds of these materials have considerable covalent character. The anhydrous salts are continuous three-dimensional networks analogous to the various polymorphic forms of siHca. Of limited commercial interest are the alurninum, boron, and iron phosphates. Boron phosphate [13308-51 -5] BPO, is produced by heating the reaction product of boric acid and phosphoric acid or by a dding H BO to H PO at room temperature, foUowed by crystallization from a solution containing >48% P205- Boron phosphate has limited use as a catalyst support, in ceramics, and in refractories. 

A continuous process has been described (14) which can produce either the amide or the nitrile by adjusting the reaction conditions. Boric acid has been used as a catalyst in the amidation of fatty acid (15). Other catalysts employed include alumina (16), titanium, and 2inc alkoxides (17). The difficulty of complete reaction during synthesis has been explained by the formation of RCOOH NH RCOO , a stable intermediate acid ammonium salt (18). 

The presence of inorganic salts may enhance or depress the aqueous solubiUty of boric acid it is increased by potassium chloride as well as by potassium or sodium sulfate but decreased by lithium and sodium chlorides. Basic anions and other nucleophiles, notably borates and fluoride, greatly increase boric acid solubihty by forrning polyions (44). 

The apparent acid strength of boric acid is increased both by strong electrolytes that modify the stmcture and activity of the solvent water and by reagents that form complexes with B(OH) 4 and/or polyborate anions. More than one mechanism may be operative when salts of metal ions are involved. In the presence of excess calcium chloride the strength of boric acid becomes comparable to that of carboxyUc acids, and such solutions maybe titrated using strong base to a sharp phenolphthalein end point. Normally titrations of boric acid are carried out following addition of mannitol or sorbitol, which form stable chelate complexes with B(OH) 4 in a manner typical of polyhydroxy compounds. EquiUbria of the type ... 

Alcohols react with boric acid with elimination of water to form borate esters, B(OR)3. A wide variety of borate salts and complexes have been prepared by the reaction of boric acid and inorganic bases, amines, and heavy-metal cations or oxyanions (44,45). Fusion with metal oxides yields... 

A number of boron chemicals are prepared directly from boric acid. These include synthetic inorganic borate salts, boron phosphate, fluoborates, boron ttihaHdes, borate esters, boron carbide, and metal aHoys such as ferroboron [11108-67-1]. 

Anhydrous metal borates may be prepared by heating the hydrated salts to 300—500°C, or by direct fusion of the metal oxide with boric acid or B2O2. Many binary and tertiary anhydrous systems containing B2O2 form vitreous phases over certain ranges of composition (145). 

Preparation. Hexagonal boron nitride can be prepared by heating boric oxide with ammonia, or by heating boric oxide, boric acid, or its salts with ammonium chloride, alkaU cyanides, or calcium cyanamide at atmospheric pressure. Elemental nitrogen does not react with boric oxide even in the presence of carbon, though it does react with elemental boron at high temperatures. Boron nitride obtained from the reaction of boron trichloride or boron trifluoride with ammonia is easily purified. 

Acid—mordant dyes have characteristics similar to those of acid dyes which have a relatively low molecular weight, anionic substituents, and an affinity to polyamide fibers and mordant dyes. In general, brilliant shades caimot be obtained by acid—mordant dyes because they are used as their chromium mordant by treatment with dichromate in the course of the dyeing procedure. However, because of their excellent fastness for light and wet treatment, they are predominandy used to dye wool in heavy shades (navy blue, brown, and black). In terms of chemical constitution, most of the acid—mordant dyes are azo dyes some are triphenyhnethane dyes and very few anthraquinone dyes are used in this area. Cl Mordant Black 13 [1324-21 -6] (183) (Cl 63615) is one of the few examples of currentiy produced anthraquinone acid—mordant dyes. It is prepared by condensation of purpurin with aniline in the presence of boric acid, followed by sulfonation and finally by conversion to the sodium salt (146,147). 

Nickel. Nickel plating continues to be very important. Many plating baths have been formulated, but most of the nickel plating is done in either Watts baths or sulfamate baths. Watts baths contain sulfate and chloride nickel salts along with boric acid, and were first proposed in 1916 (111). Nickel was first plated from sulfamate in 1938 (112) and patented in 1943 (108). The process was brought to market in 1950 (113). Typical bath compositions and conditions are shown in Table 14. 

The first in this series to be reported was 4-oxoisoxazoline-3,5-dicarboxylic acid diethyl ester, which was formed by the reaction of nitrous acid on diethyl acetonedicarboxylate in 1891. Quilico described a number of syntheses in his 1962 review and the most general include the reaction of hydroxylamine and a-hydroxy-(or acetoxy)- 3-diketones and the conversion of 4-isoxazolediazonium salts to the hydroxy moiety (62HC(17)1, p. 3). Additional syntheses reported were the oxygenation of a 4-boric acid derivative (67JOM(9)l9) and peroxide oxidation of a 4-nitro-2-isoxazoline (Scheme 151) (79ZOR2436). 

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