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Buffer capacity falls to 33% of the maximum value at pH = pK a ± 1, to 10% at pH = pK a ± 1.5 and to 1% at pH = pK a ± 2. For this reason the most useful range is approximately pK a ± 1. When choosing a buffer for use at a specific pH, it should have a pK a value as close as possible to that pH. [2]
Free Fire Max is an enhanced version of Free Fire that was released in 2021. [71] [72] It features improved High-Definition graphics, sound effects, and a 360-degree rotatable lobby. Players can use the same account to play both Free Fire Max and Free Fire, and in-game purchases, costumes, and items are synced between the two games. [73]
On December 9, 2021, at The Game Awards, Google announced that Google Play Games beta would launch in early 2022, bringing Android games to Windows PCs and laptops. [10] The minimum specification requirements to run Google Play Games are currently Windows 10 or later operating system with an integrated graphics card and quad-core CPU that can access Google Play Games beta (previously octo-core ...
McIlvaine buffer is a buffer solution composed of citric acid and disodium hydrogen phosphate, also known as citrate-phosphate buffer.It was introduced in 1921 by the United States agronomist Theodore Clinton McIlvaine (1875–1959) from West Virginia University, and it can be prepared in pH 2.2 to 8 by mixing two stock solutions.
Borate buffered saline (abbreviated BBS) is a buffer used in some biochemical techniques to maintain the pH within a relatively narrow range. Borate buffers have an alkaline buffering capacity in the 8–10 range. Boric acid has a pK a of 9.14 at 25 °C.
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The Britton–Robinson buffer (BRB or PEM) is a "universal" pH buffer used for the pH range from 2 to 12. It has been used historically as an alternative to the McIlvaine buffer , which has a smaller pH range of effectiveness (from 2 to 8).
Aminomethyl propanol is used for the preparation of buffer solutions. [3] It is a component of the drugs ambuphylline and pamabrom.It is also used in cosmetics. [2]It is a precursor to oxazolines via its reaction with acyl chlorides. [5]