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Boric acid, B

Table 5. Thermodynamic Properties of Crystalline Boric Acid, B(OH)3 ... Table 5. Thermodynamic Properties of Crystalline Boric Acid, B(OH)3 ...
Boric acid [B(OH)3] is employed in primary coolant systems as a soluble, core reactivity controlling agent (moderator). It has a high capture cross-section for neutrons and is typically present to the extent of perhaps 300 to 1,000 ppm (down from perhaps 500 to 2,500 ppm 25 years ago), depending on nuclear reactor plant design and the equilibrium concentration reached with lithium hydroxide. However, boric acid may be present to a maximum extent of 1,200 ppm product in hot power nuclear operations. [Pg.477]

In presence of 3.45 x 10-3 M boric acid. b HC104 used for these runs. [Pg.296]

Draw the Lewis structure for boric acid, B(OH),. (a) Is resonance important for its description (b) The proton transfer equilibrium for boric acid is given in a footnote to Table 10.1. [Pg.562]

Boric acid, B(OH) , is a white solid that melts at 171°C. It is toxic to bacteria and many insects as well as humans and has long been used as a mild antiseptic and pesticide. Because the boron atom in B(OH)3 has an incomplete octet, it can act as a Lewis acid and form a bond by accepting a lone pair of electrons from an H20 molecule acting as a Lewis base ... [Pg.720]

Although the complete description of its structure will not be shown here, boric acid, B(OH)3, has a sheet structure in which each boron atom resides in a trigonal planar environment of oxygen atoms. There is hydrogen bonding between the OH groups in neighboring molecules. [Pg.123]

Boric acid, B(OH)3 is a Lewis acid with pKa = 9.0. A hydroxyl group is added to the trigonal boric acid molecule forming a tetrahedral borate ion ... [Pg.151]

Q VSUB Boric acid, B(OH)3(aq), is used as a mild antiseptic in eye-wash solutions. The following reaction takes place in aqueous solution. [Pg.387]

Coordination Number Three. These include planar complex ions such as boric acid B(OH)3 and out-of-plane pyramidal complexes (including SnCl3 ). [Pg.169]

Yamamoto reported the first boron reagent-based catalytic method that allows direct amide formahon from a free carboxylic acid and amine as the reaction partners [21]. Aryl boronic acid derivahves bearing electron-withdrawing subshtu-ents in the meta and/or para posihons were found to be the catalyst of choice for these kinds of transformations. Tang s work [22] featured the use of a cheap, readily available, non-toxic, and eco-friendly boric acid, B(OH)i, as a highly effective catalyst that proved to be superior to other known catalysts involved in the amidation process. [Pg.297]

How many grams of boric acid, B(OH), (FM 61.83), should be used to make 2.00 L of 0.050 0 M solution What kind of flask is used to prepare this solution ... [Pg.19]

Boric acid, B(OH)3, is a white solid that melts at 171°C. It is toxic to bacteria and many insects as well as humans and has long been used as a... [Pg.823]

Tetra(Hydrogen Sulfato)Boric Acid-Sulfuric Acid. HB(HS04)4 prepared by treating boric acid, B(OH)3, with sulfuric acid ionizes in sulfuric acid as shown by acidity measurements7 [Eq. (2.19)]. [Pg.47]

This group has symmetry element E, a rotational axis C , and a horizontal plane <7h perpendicular to C . Note that S also exists as a consequence of the elements already present (C and of,). Also, when n is even, the presence of i is again a necessary consequence. Examples include trans-N2F2 (C 21, Fig. 6.1.6), all-trans-1,5,9-cyclododecatricne (C 3h Fig. 6.1.7), and boric acid B(OH)3 (C h Fig. 13.5.1). [Pg.172]

Boric acid, B(OH)3, is the archetype and primary source of oxo-boron compounds. It is also the normal end product of hydrolysis of most boron compounds. It forms flaky, white and transparent crystals, in which the BO3 units are joined to form planar layers by O-H- O hydrogen bonds, as shown in Fig. 13.5.1. [Pg.486]

Boron is devoid of metallic character in water, it generates weakly acidic boric acid [B(OH)3]. This hydroxide bonds covalently with vicinal (neighboring) hydroxyl groups to form negatively charged, acidic complexes. [Pg.107]

B = 0 bonds may be present. The hydoxide boric acid B(OH)3 is formed by the hydrolysis of many boron compounds. It has a layer structure made up of planar molecules linked by hydrogen bonding. It is a... [Pg.152]

Effects of hydrogen bonding on physical and chemical properties. Hydrogen bonding produces many physical and chemical effects. The added intermolecular interaction often produces a drastic effect on melting and boiling points. For example, H20 boils at 100°C and H2S boils at -61 °C. BF3 is a gas (m.p. -127°C, b.p. -101 °C), whereas boric acid, B(OH)3, is a solid that decomposes at 185 °C. [Pg.82]

Hydrolysis of B203 generates orthoboric acid (boric acid), B(OH)3, another major commercial product that is manufactured on a scale of hundreds of thousands of tons per year by acidification of aqueous solutions of borax, a naturally occurring mineral (see Section 5-2). Crystalline B(OH)3 contains planar BO3" units (Fig. [Pg.171]

Boric acid, B(OH)3, or H3BO3, is the only boric acid of commercial sigiuficance. It is also referred to as orthoboric acid, bnt nsnally only when context requires specifying this particnlar form. It can also be written as B2O3 3H2O, emphasizing the relationship with its acid anhydride B2O3. [Pg.424]


See other pages where Boric acid, B is mentioned: [Pg.203]    [Pg.137]    [Pg.474]    [Pg.195]    [Pg.196]    [Pg.296]    [Pg.350]    [Pg.500]    [Pg.46]    [Pg.3]    [Pg.282]    [Pg.1547]    [Pg.58]    [Pg.5]    [Pg.19]    [Pg.175]    [Pg.175]    [Pg.682]    [Pg.1151]    [Pg.5]    [Pg.605]    [Pg.649]    [Pg.304]    [Pg.127]    [Pg.87]    [Pg.492]    [Pg.5]    [Pg.43]   
See also in sourсe #XX -- [ Pg.3 , Pg.203 ]

See also in sourсe #XX -- [ Pg.3 , Pg.203 ]




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