Sodium Tungstate Dihydrate-VII

The same approach can be used for primary alcohols. However, in the case of primary benzylic alcohols, the amount of hydrogen peroxide used affects the final product. Noyori and co-workers reported that when a small amount of hydrogen peroxide (< 1.5 molar amount) is used to oxidize primary benzylic alcohols, the corresponding aldehydes can be obtained; if a higher amount of hydrogen peroxide (2.5 - 5 molar amount) is added, the corresponding benzoic acids can be produced. The efficiency is highly dependent on the electronic propertiesof substituents.


 

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Poly Tungsten Shields for Highly-Skilled Injection Molding

For many decades, lead (Pb) was the best option for protecting against radiation. It was cheap and plentiful, but it was toxic and highly-hazardous. Manufacturing with lead is currently banned in Europe, and is on track to be banned in the U.S. Poly tungsten shields are effectively and safely shield against radiation, that alternative for lead shields.

Proprietary combination of tungsten and polymers called poly tungsten has been developed. Poly tungsten shields against radiation even better than lead does —but far more safely. Poly tungsten has the same density as lead, meaning it can shield radiation at the same level as lead. It retains its shape during use, and can be used in many applications. Poly tungsten is safe and reliable.

Injection-molded poly tungsten parts have been successfully used in:
CT scanners
X-ray machines
Radiation therapy
Nuclear medicine equipment.

 

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Sodium Tungstate Dihydrate-VI

c) Oxidation of alcohols
Secondary alcohols can be converted into the corresponding ketones (83-96% yield) under biphasic conditions (organic/aqueous) using 30% hydrogen peroxide in the presence of sodium tungstate dihydrate as catalyst and an appropriate PTC such as [CH3-(n-C8H17)3N]HSO4. Noyori and co-workers studied several cases with alkyl or aryl groups, namely 2-octanol or 1-phenylethanol, under solvent-free conditions or using toluene as solvent.


 

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Sodium Tungstate Dihydrate-V

Recently, a catalytic system based on Na2WO4.2H2O/CH3CO2H/H2O2 was developed as an effective method to oxidize natural rubber (with a large number of carbon-carbon double bonds in its structure) into the corresponding epoxy derivatives. This catalytic system possesses much higher epoxidation efficiency than the traditional CH3CO2H/H2O2 system. The proposed method also induces further oxidation of the epoxides into the corresponding ketones and aldehydes, resulting from C-C cleavage.


 

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Sodium Tungstate Dihydrate-IV

b) Cleavage of double bonds (to carboxylic acids, aldehydes or ketones)

A convenient and efficient method for converting cyclohexene into adipic acid has been reported. This protocol represents a new and green viewpoint for the synthesis of adipic acid, since this approach replaces usual hazardous oxidizing agents, such as nitric acid, for an environmentally benign one, aqueous hydrogen peroxide. When a mixture of cyclohexene, hydrogen peroxide, sodium tungstate dihydrate and [CH3(n-C8H17)3N]HSO4 as PTC is kept at 75ºC to 90 ºC for 8 hours, adipic acid is obtained in 93% yield. Adipic acid is an importantchemical, whose production is necessary for the manufacture of nylon-6,6. This procedure is equally applicable to the oxidation of substituted cyclohexenes. Moreover, the oxidation cyclopentene produced crystalline glutaric acid in 90% yield.


 

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Sodium Tungstate Dihydrate-III

The epoxidation of 1,4-bis(allyloxy)butane in the presence of sodium tungstate dihydrate and orthophosphoric acid gives 1-allyloxy-4-glycidoloxybutane and 1,4-bis(glycidoloxy)butane under phase transfer conditions, using 30% hydrogen peroxide as oxidant. Methyltrioctylammonium chloride (Aliquat 336) was used as phase transfer catalyst (PTC). Sodium tungstate dihydrate can be used also as catalyst in the epoxidation of terpenes, such as limonene, geraniol, nerol or 3-carene, using a phosphate buffer solution of H3PO4/NaH2PO4.


 

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Sodium Tungstate Dihydrate-II

2. Applications
Sodium tungstate dihydrate can be used as catalyst or as catalyst precursor in several organic reactions, namely:

a) Epoxidation
The sodium tungstate catalyzed epoxidation of α,β-unsaturated acids by hydrogen peroxide in water has been developed by Payne in 1959, and revisited by Sharpless in 1985, also in water. According to Sheldon, the epoxidation of allyl alcohol to glycidol using hydrogen peroxide and sodium tungstate was applied industrially as an alternative to thetraditional route via epichlorohydrin. The epoxidation procedure developed by Venturello and co-workers, using a Na2WO4.2H2O/H3PO4/quaternary ammonium chloride/aqueous 8% hydrogen peroxide system presents some drawbacks, since requires an excess of olefinic substrates and uses 1,2-dichloroethane, a toxic and carcinogenic chlorinated hydrocarbon solvent. In contrast, Noyori and co-workers reported a clean, halide-free, biphasic epoxidation method with 30% hydrogen peroxide in the presence of sodium tungstate dihydrate, (aminomethyl)phosphonic acid, and a phase transfer catalyst (PTC) such as Q+HSO4- (Q+ =CH3(n-C8H17)3N+) to epoxidize olefins such as cyclooctene (98% yield) or 1-dodecene (87% yield). Functionalized olefins containing an ester, ether, alcohol, or α,β-enone linkage in the same molecule can also be epoxidized by this procedure.


 

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Sodium Tungstate Dihydrate-I

1.Introduction
Sodium tungstate dihydrate is a commercially available reagent which exists in the form of a crystalline white solid. Sodium tungstate dihydrate is usually used in the synthesis of inorganic compounds, namely in polyoxometalates synthesis. It can also be used in organic chemistry as a green catalyst or catalyst precursor, since sodium tungstate dihydrate is able to catalyze the oxidation of several substrates in the presence of hydrogen peroxide, generating only water as the by-product (Scheme 1). On the other hand, the conjugation of this reagent with other inorganic reagents used in polyoxometalates synthesis permits the formation of several complexes, mainly peroxocomplexes, which can catalyze some oxidation reactions by themselves.


 

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Tungsten Carbide V-Shaped Bits

Tungsten carbide v-shaped bits are referred to the bits that made of tungsten carbide and typically used for signs and V-carving. Generally, there are two factors,which are likely to affect the profile of the v-bits, angle and diameter.



Angle

It is commonly referred to the included angle. The most well accept angle of v-bits are 30°, 45°,60°, 90°, and 120°. The relevant tip of a V-bit presents as a true point, a small radius or a flat.

Diameter

It is the width of a full depth cut at the surface of the workpiece, measured perpendicular to the shank.


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Uses of Tungstic Acid-VIII

Tungsten acid can be used for co-solvents.

A second solvent added in small quantities to enhance the solvent power of the primary solvent.

Common co-solvents have two categories: one is certain organic acids and sodium salts, such as sodium benzoate, sodium salicylate, p-amino benzoic acid; the other is amides, such as urea , nicotinamide, acetamide. The solubilization mechanism is complex, many of the which is still unclear, therefore, there is no clear rules to follow on the selection of co-solvent, generally choose the substances that can obtain water-soluble molecular complexes rehabilitation salt or association complex according to the nature of drugs.


 

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