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Metasilicate

Fig. 1. Examples of stmctures for silicates (a) monomer where is present (b) metasilicates where is present and (c) branched-ring... Fig. 1. Examples of stmctures for silicates (a) monomer where is present (b) metasilicates where is present and (c) branched-ring...
When every Si04 shares 2 O with contiguous tetrahedra, metasilicates of empirical... [Pg.348]

Chain metasilicates Si03 formed by comersharing of Si04 tetrahedra arc particularly prevalent in nature and many important minerals have this basic structural unit (cf, polyphosphates, p, 528), Despite the apparent simplieily of their structure motif and stoichiometry considerable structural diversity is encountered because of the differing conformations that can be adopted by the linked tetrahedra. As a result, the repeat distance along the c -axis can be (1). [Pg.349]

Figure 9.6 Schematic representation and exampies of various chain metasilicates (SiO with repeat distances (in pm) after i, 2,. 7. 9 or 12 tetrahedra (T), ((ht) high-temperature form (hp) high-pressure form]. Figure 9.6 Schematic representation and exampies of various chain metasilicates (SiO with repeat distances (in pm) after i, 2,. 7. 9 or 12 tetrahedra (T), ((ht) high-temperature form (hp) high-pressure form].
Pure NI3 has not been isolated, but the structure of its well-known extremely shock-sensitive adduct with NH3 has been elucidated — a feat of considerable technical virtuosity.Unlike the volatile, soluble, molecular solid NCI3, the involatile, insoluble compound [Nl3.NH3] has a polymeric structure in which tetrahedral NI4 units are comer-linked into infinite chains of -N-I-N-I- (215 and 230 pm) which in turn are linked into sheets by I-I interactions (336 pm) in the c-direction in addition, one I of each NI4 unit is also loosely attached to an NH3 (253 pm) that projects into the space between the sheets of tetra-hedra. The stmcture resembles that of the linked Si04 units in chain metasilicates (p. 349). A further interesting feature is the presence of linear or almost linear N-I-N groupings which suggest the presence of 3-centre, 4-electron bonds (pp. 63, 64) characteristic of polyhalides and xenon halides (pp. 835-8, 897). [Pg.441]

Locomotive diesels As larger volumes of coolant are required in railway locomotives than in road vehicles, the cost of inhibition is proportionally greater. An additional factor is the possibility of cavitation attack of cylinder liners. These considerations place a restriction on the choice of inhibitors. In the past, chromates have been used at concentrations of up to 0-4%, but their use presents handling and disposal problems. Chromates cannot be used with ethanediol antifreeze solutions. A IS I borate-metasilicate at a concentration of 1 % has been used in the UK. Nitrate is added to this to improve inhibition of aluminium alloy corrosion. Tannins and soluble oils are also used, but probably to a lesser extent than in the past. The benzoate-nitrite formulation (formerly BS 3151) is effective and has been used by continental railways . ... [Pg.790]

Lack of BD control High treatment/small boiler Poor design, lead and lag boiler operation scale and ferrous metasilicate FeSi03 Water losses, low inhibitor levels Surging/carryover from high TDS. Excessive TDS in lead boiler. Lack of treatment in lag boiler. [Pg.188]

When soluble iron is present in FW that also contains silica, the iron may be transported through to the boiler, where insoluble ferrous metasilicate (FeSi03) preferentially forms instead of magnetite. [Pg.214]

Magnetite is unstable relative to ferrous metasilicate (FeSi03) and so, under certain high-silica BW conditions, ferrous metasilicate may form in preference to magnetite. Iron silicate scales are exceedingly insoluble and adherent. [Pg.230]

Orthosilicates are not suitable for corrosion inhibitor purposes, and metasilicates are not generally used because they tend to increase the caustic alkalinity too much, leading to the potential for caustic-induced problems. However, glassy polysilicates are widely used. They have inhibition properties similar to those of polyphosphates and also have an indefinite crystalline structure. [Pg.398]

Sodium metasilicate, Na2Si03, or in the hydrated form, Na2Si03-9H20... [Pg.652]

Addition of suitable builders, such as sodium silicates or sodium tripolyphosphate, could increase the detergency of soap-LSDA blend even further. A systematic investigation of three-component systems, soap-LSDA builder, showed that a detergency maximum could be attained which corresponded to a certain fixed ratio of components. Maximum detergency corresponded to an approximate composition of 75% soap, 10% MES, and 15% metasilicate. The tests were carried out at 50°C and at 300 ppm water hardness which is well above that of U.S. municipal water supplies. The principle of detergency potentiation of soap by an LSDA and builder was always evident, even when using other artificially soiled cloths, such as those supplied by U.S. Testing Co. or Testfabrics Inc. [Pg.639]

FIG. 2 Detergency (AR) behavior of the three-component system soap, sodium metasilicate, sodium methyl a-sulfotallowate (0.2% total detergent concentration, 50°C, 300 ppm water hardness, EMPA-101 cotton cloth). [Pg.640]

Amphoteric LSDA Sodium metasilicate Sodium sulfate Carboxymethylcellulose Additives... [Pg.641]

Addition of as little as 5% soap to an amphoteric LSDA of limited water solubility (high Krafft point) brought about a substantial lowering of the Krafft point and thus markedly improved water solubility. On the other hand, addition of 10% of amphoteric LSDA to sodium palmitate lowered the Krafft point of the soap by 10-14°C. Addition of anionic LSDA to sodium palmitate showed smaller Krafft point depression. Addition of a builder-type salt, such as sodium metasilicate, had essentially no effect on the Krafft points of soap-LSDA mixtures. [Pg.642]

The silicates which will occur are orthosilicates, R++2Si04, metasilicates, R++Si03, etc. This is verified by observation no basic silicates of such cations are known, although many normal silicates such as forsterite Mg2Si04, etc., exist. [Pg.297]

Ball-and-stick representations of two forms of metasilicates, the six-Si ring of beryl left) and a portion of the linear chain of jade right). [Pg.614]

C09-0139. Describe the bonding differences among silica, silicate minerals, and metasilicate minerals. [Pg.654]


See other pages where Metasilicate is mentioned: [Pg.365]    [Pg.187]    [Pg.148]    [Pg.574]    [Pg.906]    [Pg.4]    [Pg.75]    [Pg.473]    [Pg.383]    [Pg.349]    [Pg.349]    [Pg.350]    [Pg.529]    [Pg.821]    [Pg.284]    [Pg.789]    [Pg.791]    [Pg.182]    [Pg.650]    [Pg.858]    [Pg.896]    [Pg.945]    [Pg.206]    [Pg.271]    [Pg.733]    [Pg.937]    [Pg.292]    [Pg.297]    [Pg.614]   
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See also in sourсe #XX -- [ Pg.152 ]

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See also in sourсe #XX -- [ Pg.60 ]

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Barium metasilicate

Calcium metasilicate

Calcium metasilicate filler

Crystallity hydrated sodium metasilicates

Crystallization sodium metasilicate solution

Disodium metasilicate

Dried silicate solutions metasilicates

Granulated sodium metasilicates

Lead chloride metasilicate

Lithium metasilicate

Lithium-metasilicate crystals

Magnesium hydrogen metasilicate

Magnesium metasilicate

MetaSil

MetaSil

MetaSil Basic

MetaSilicate, lead

MetaSilicate, lead lithium

MetaSilicate, lead sodium

Metasilicate granulated

Metasilicate pentahydrate

Metasilicate spectrum

Metasilicates

Potassium metasilicate

Silicates and Metasilicates

Silicates metasilicates

Sodium metasilicate

Sodium metasilicate pentahydrate

Sodium metasilicate, anhydrous

Sodium metasilicate, food additive

Sodium metasilicate, granulated

Sodium metasilicate, zeolite

Sodium tripolyphosphate metasilicate

Wollastonite (Calcium Metasilicate)

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