Aqua Chemical

Ingredient aqua Chemical meaning water Purpose solvent... 

At the initial stage of the in situ formation of organic aerosol, an aqua-chemical interaction of hydrocarbon molecules is supposed to take place with such atmospheric oxidizers as Oj, OH, NOx [31]. 

Aquaness Chemicals Aquatec Quimica SA Arizona Chemical Co. 

Aqua Chemical Brainerd Chemical Bruchem Coyne Chemical Puritan Products Warner Graham... 

Tetrafluoroethylene. Emulsion polymerisation of tetrafluoroethylene, catalysed by oxygen, yields polytetrafluoroethylene (Tejlon) as a very tough horn-hke material of high melting point. It possesses excellent electrical insulation properties and a remarkable inertness towards all chemical reagents, including aqua regia. 

United States Pharmacopeia stronger ammonia water ammonia test solution normal (1 N) aqua ammonia chemically pure technical, Bh°... 

The corrosion behavior of tantalum is weU-documented (46). Technically, the excellent corrosion resistance of the metal reflects the chemical properties of the thermal oxide always present on the surface of the metal. This very adherent oxide layer makes tantalum one of the most corrosion-resistant metals to many chemicals at temperatures below 150°C. Tantalum is not attacked by most mineral acids, including aqua regia, perchloric acid, nitric acid, and concentrated sulfuric acid below 175°C. Tantalum is inert to most organic compounds organic acids, alcohols, ketones, esters, and phenols do not attack tantalum. 

The chemical resistance of PTFE is almost universal It resists attack by aqua regia, hot fummg nitnc acid, hot caustic, chlorine, chlorosulfonic acid, and all solvents. Despite this broad chemical resistance, PTFE is attacked by molten alkali metals, ammonia solutions of such metals, chlorine trifluoride, and gaseous fluonne at elevated temperature and pressure PTFE swells or dissolves m certam highly fluonnated oils near its melting point. Specific lists of chemicals compatible with PTFE are available [/.8]... 

We employed malononitrile and l-crotonoyl-3,5-dimethylpyrazole as donor and acceptor molecules, respectively. We have found that this reaction at room temperature in chloroform can be effectively catalyzed by the J ,J -DBFOX/Ph-nick-el(II) and -zinc(II) complexes in the absence of Lewis bases leading to l-(4,4-dicya-no-3-methylbutanoyl)-3,5-dimethylpyrazole in a good chemical yield and enantio-selectivity (Scheme 7.47). However, copper(II), iron(II), and titanium complexes were not effective at all, either the catalytic activity or the enantioselectivity being not sufficient. With the J ,J -DBFOX/Ph-nickel(II) aqua complex in hand as the most reactive catalyst, we then investigated the double activation method by using this catalyst. 

As shown above, it was not so easy to optimize the Michael addition reactions of l-crotonoyl-3,5-dimethylpyrazole in the presence of the l ,J -DBFOX/ Ph-Ni(C104)2 3H20 catalyst because a simple tendency of influence to enantio-selectivity is lacking. Therefore, we changed the acceptor to 3-crotonoyl-2-oxazolidi-none in the reactions of malononitrile in dichloromethane in the presence of the nickel(II) aqua complex (10 mol%) (Scheme 7.49). For the Michael additions using the oxazolidinone acceptor, dichloromethane was better solvent than THF and the enantioselectivities were rather independent upon the reaction temperatures and Lewis base catalysts. Chemical yields were also satisfactory. 

The resistance of rhodium to chemical attack is remarkable, and surpasses that of platinum. Its domain of stability (as seen from Fig. 6.4) is extremely wide, and in the absence of complexing agents it is stable in aqueous solutions of all pH values. In the massive form it is unattacked by caustic alkalis, acids and oxidising agents, including aqua regia. When finely divided, however, it is attacked by concentrated sulphuric acid and aqua regia. 

Shimizu et al. (56) studied the biosynthesis of the STX analog neoSTX using Aph, flos-aquae NH-1. They were able to confirm its presence in strain NH-1 and to explain the biosynthetic pathway for this important group of secondary chemicals. 

In the presence of potassium chlorate/nitric acid/hydrochloric acid mixture, ruthenium oxidises expiosively. Ruthenium is chemically inert like any noble metal and maybe more than any other metal. Indeed, it is inactive vis- -vis aqua regia , but on this occasion potassium chlorate was combined with aqua regia. 

American Chemical Society. Aqua regia. Available online. URL http //jchemed.chem.wisc.edu/JCEsoft/CCA/CCA3/MAIN/ AQREGIA/PAGE1.HTM. Accessed on January 21, 2008. 

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