Alkali sodium silicate

A few studies considered the effect of pH on the viscosity of xanthan solutions. Jeanes et al. observed a rapid increase in the viscosity of xanthan solution at pH 9-11 [28]. Whitcomb and Macosko [29] and Philips et al. [30] found the viscosity of xanthan to be independent of pH. Szabo examined the stability of various EOR polymers in caustic solutions at room temperature, including Kelzan MF (a biopolymer) [6]. He found a fast initial drop in the viscosity of a xanthan solution containing 2 wt% sodium chloride and 5 wt% sodium hydroxide, at 12.5 s", which virtually stopped after 10 days. Krumrine and Falcone found that the effect of alkali (sodium silicates) on the viscosity of xanthan solution depended on the concentration of sodium and calcium ions present [31]. Ryles examined the thermal stability of bio-polymers in alkaline conditions [16]. He found that xanthan was totally degraded (in anaerobic conditions) upon the addition of 0.8 wt% sodium hydroxide at temperatures from 50 to 90°C (in a 1 wt% sodium chloride brine). Seright and Henrici observed total biopolymer degradation at pH > 8 and a temperature of 120°C [26]. 

The alkali silicates are soluble in water and are used industrially. See sodium silicates. 

Sulphates, silicates, carbonates, colloids and certain organic compounds act as inhibitors if evenly distributed, and sodium silicate has been used as such in certain media. Nitrates tend to promote corrosion, especially in acid soil waters, due to cathodic de-polarisation and to the formation of soluble nitrates. Alkaline soils can cause serious corrosion with the formation of alkali plumbites which decompose to give (red) lead monoxide. Organic acids and carbon dioxide from rotting vegetable matter or manure also have a strong corrosive action. This is probably the explanation of phenol corrosion , which is not caused by phenol, but thought to be caused by decomposition of jute or hessian in applied protective layers. ... 

Rapid fixation in 5-8 hours using a mixture of sodium hydroxide and sodium silicate, a metering pump being necessary. A high concentration of alkali gives rapid fixation but still allows excellent bath stability at temperatures up to 30 °C. 

Fixation in 6-12 hours with a mixture of sodium hydroxide and trisodium orthophosphate, a metering device being necessary. This method is recommended for regenerated cellulosic fibres. This formulation contains the same total amount of alkali as method (1) with the same bath stability, but may be preferred where some buffering capacity is required and sodium silicate is undesirable. 

In general the prospect of working without silicate is regarded as a major advantage because the padding and washing-off of sodium silicate places considerable stresses on the machinery and on effluent treatment. However, the use of silicate in no way impairs the performance of Levafix dyes. Six optimised alkali recipes for this system are shown in Table 12.17, whilst Table 12.18 shows the relation between pad liquor pH, batching time and pad liquor stability. 

Washing machines currently on the market are constructed almost exclusively with drums and laundry tubs of corrosion-resistant stainless steel or with an enameled finish that is inert to alkaline wash liquors. Nevertheless, various machine components are made of less detergent resistant metals or alloys. To prevent corrosion of these parts, modern detergents contain corrosion inhibitors in the form of sodium silicate. The colloidal silicate that is present, deposits as a thin, inert layer on metallic surfaces, thereby protecting them from attack by alkali. 

Siroc [Silicate rock] Also known as the one-shot system. A chemical grouting system for hardening ground formations. Aqueous solutions of sodium silicate and formamide are mixed and injected into the ground the formamide slowly reacts with the silicate, precipitating hydrated silica, which binds the soil particles together. Invented in 1961 by the Diamond Alkali Company. See also Joosten. 

The product of the fusion of silica with sodium carbonate, sodium silicate (strictly called sodium poly trioxosilicate but usually metasilicate), dissolves in water to give a clear, viscous solution known as waterglass . It hydrolyses slowly and silica is precipitated. Besides the metasilicate, other silicates of sodium are known, e.g. the poly-tetroxosilicate (orthosilicate), Na4Si04. Only the silicates of the alkali metals are soluble in water. Other silicates, many of which occur naturally, are insoluble, and in these substances the polysilicate anions can have highly complicated structures, all of which are constructed from a unit of one silicon and four oxygen atoms arranged tetrahedrally (cf. the structure of silica). Some of these contain aluminium (the aluminatesilicates) and some have import ant properties and uses. 

The significant increase in the use of supplementary cementing materials (such as fly ash and slag) in the last decade has dictated the need for an admixture that can offset the slowed hydration that results when such materials are incorporated in concrete. Strong basic salts such as sodium aluminate, alkali hydroxides, silicates, sulfates and thiosulfates have shown some promise. A number of proprietary admixtures which claim to catalyze the pozzalanic and thereby increase the rate of hydration are now marketed. 

Based on the discussion of the previous section, we would also expect that structural complexity and disorder present in glasses would tend to decrease the thermal conductivity. This is true, especially when alkalis are added to sodium silicate glasses. Figure 4.32 shows the effect of replacing SiOa in Na20-Si02 glass with other oxides. 

J. Reich 6 also patented a process based on the calcination of the alkali fluosilicate or fluoborate with an oxide of the alkaline earths. When the calcined mass is lixiviated with water, the alkali fluoride is obtained in soln. L. Schuch 6 made sodium fluoride by boiling finely powdered cryolite with a cone. soln. of sodium hydroxide—the alumina and silica pass into soln.—sodium fluoride crystallizes from the cooling soln. Sodium silicate can be used in place of the hydroxide. F. Jean made sodium fluoride by leaching a calcined mixture of fluorspar, limestone, Glauber s salt, and charcoal. 

Silicon carbide is comparatively stable. The only violent reaction occurs when SiC is heated with a mixture of potassium dichromate and lead chromate. Chemical reactions do, however, take place between silicon carbide and a variety of compounds at relatively high temperatures. Sodium silicate attacks SiC above 1300°C, and SiC reacts with calcium and magnesium oxides above 1000°C and with copper oxide at 800°C to form the metal silicide. Silicon carbide decomposes in fused alkalies such as potassium chromate or sodium chromate and in fused borax or cryolite, and reacts with carbon dioxide, hydrogen, air, and steam. Silicon carbide, resistant to chlorine below 700°C, reacts to form carbon and silicon tetrachloride at high temperature. SiC dissociates in molten iron and the silicon reacts with oxides present in the melt, a reaction of use in the metallurgy of iron and steel (qv). The dense, self-bonded type of SiC has good resistance to aluminum up to about 800°C, to bismuth and zinc at 600°C, and to tin up to 400°C a new silicon nitride-bonded type exhibits improved resistance to cryolite. 

Synthesis of MCM-41 with Additives. The hydrothermal crystallization procedure as described earlier [10] was modified by adding additional salts like tetraalkylammonium (TAA+) bromide or alkali bromides to the synthesis gel [11]. Sodium silicate solution ( 14% NaOH, 27% Si02) was used as the silicon source. Cetyltrimethylammonium (CTA) bromide was used as the surfactant (Cl6). Other surfactants like octadecylltrimethylammonium (ODA) bromide (C,8), myristyltrimethylammonium (MTA) bromide (C,4) were also used to get MCM-41 structures with different pore diameter. Different tetralkylammonium or alkali halide salts were dissolved in little water and added to the gel before addition of the silica source. The final gel mixture was stirred for 2 h at room temperature and then transferred into polypropylene bottles and statically heated at 100°C for 4 days under autogeneous pressure. The final solid material obtained was washed with plenty of water, dried and calcined (heating rate l°C/min) at 560°C for 6 h. 

The weathering of surface rocks has had a critical role in the chemical evolution of the continental crust for most of the Earth s history. In the presence of air and water, mafic minerals tend to rapidly weather into iron (oxy)(hydr)oxides, clays, and other silicate minerals, and at least partially water-soluble salts of alkalis (sodium and potassium) and alkaline earths (calcium and magnesium). In contrast, quartz in felsic and intermediate igneous rocks is very stable in the presence of surface air and water, which explains why the mineral readily accumulates in sands and other sediments. 

Sol-gel silica synthesis is based on the controlled condensation of Si(OH)4 entities. These may be formed by hydrolysis of soluble alkali metal silicates or of alkoxysilanes. The commonly used compounds are sodium silicates and tetraethoxysilane (TEOS). 

Essentially, all primary skin irritants include acids, alkalis, metals, salts, and solvents. Among organic acids one may include acetic acid, acrylic acid, carbolic acid, chloroacetic acid, formic acid, lactic acid, oxalic acid, and salicylic acid. Among inorganic acids one may list arsenious acid, chromic acid, hydrochloric acid, hydrofluoric acid, nitric acid, phosphoric acid, and sulfuric acid. Alkalis include butylamines, ethylamines, ethanolamines, methylamines, propylamines, and triethanolamine. One also may include ammonium carbonate, ammonium hydroxide, calcium carbonate, calcium cyanamide, calcium hydroxide, calcium oxide, potassium carbonate, potassium hydroxide, sodium carbonate (soda ash), sodium hydroxide (caustic soda), and sodium silicate. 

These natural minerals are alkali aluminum silicates and have been used as molecular sieves and cation exchangers. Recently they have been used to control some organic photochemical reactions, du Pont chemists1 have prepared lithiated zeolites by treatment of sodium aluminum silicates such as zeolite 13X with LiNO,. These silicates, designated Li-X and Li-Y, can effect rearrangement of a-alkyl-deoxybenzoins top-alkylbenzophenones in nearly quantitative yield. Thus photolysis... 

Inorganic zinc-rich primers consist of zinc and a reactive binder such as an alkali metal silicate (sodium, potassium, lithium or quaternary ammonium silicate) or hydrolyzed ethyl silicate as binder. On mixing hard and cohesive films of silicate are formed. The structure of the inorganic zinc-rich silicate may appear as shown in Figure 1.66. 

The adverse effects of alkali on wool cause reduction in its dry strength only after fiber solubilization and considerable loss in its cystine content (105). Because of its sensitivity to alkali, wool is preferentially given a peroxide bleach with added formic acid silk does not degrade nearly so much under alkaline conditions and may be bleached at pH 10 with peroxide, using stabilizers such as sodium silicate (98). 

---