Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pentaerythritol unit

The inherent chirality of the M(bpy)3 motif is a disadvantage when it comes to multi-nuclear compounds as these will be formed as mixtures of diastereomers unless special conditions are used to optimize stereospecificity. In contrast, M(tpy)2 units linked through the 4 -position are achiral and are an ideal motif for the linear extension of achiral metallostars. Metallostars based upon pentaerythritol units are discussed in detail in Section 7.6.6.2. [Pg.279]

The nameplate capacities for acetaldehyde production for the United States in 1989 are shown in Table 5 (120). Synthetic pyridine derivatives, peracetic acid, acetate esters by the Tischenko route, and pentaerythritol account for 40% of acetaldehyde demand. This sector may show strong growth in some products but all of these materials maybe prepared from alternative processes. [Pg.53]

Production of pentaerythritol in the United States has been erratic. Demand decreased in 1975 because of an economic recession and grew only moderately to 1980 (69). The range of uses for pentaerythritol has grown rapidly in lubricants (qv), fire-retardant compositions, adhesives, and other formulations where the cross-linking capabiUties are of critical importance. [Pg.466]

The world s largest producers are Perstorp AB (Sweden, United States, Italy), Hoechst Celanese Corporation (United States, Canada), Degussa (Germany), and Hercules (United States) with estimated 1989 plant capacities of 65,000, 59,000, 30,000, and 22,000 t/yr, respectively. Worldwide capacity for pentaerythritol production was 316,000 t in 1989, about half of which was from the big four companies. Most of the remainder was produced in Asia (Japan, China, India, Korea, and Taiwan), Europe (Italy, Spain), or South America (Brazil, Chile). The estimated rate of production for 1989 was about 253,000 t or about 80% of nameplate capacity. [Pg.466]

The basic metal salts and soaps tend to be less cosdy than the alkyl tin stabilizers for example, in the United States, the market price in 1993 for calcium stearate was about 1.30— 1.60, zinc stearate was 1.70— 2.00, and barium stearate was 2.40— 2.80/kg. Not all of the coadditives are necessary in every PVC compound. Typically, commercial mixed metal stabilizers contain most of the necessary coadditives and usually an epoxy compound and a phosphite are the only additional products that may be added by the processor. The requited costabilizers, however, significantly add to the stabilization costs. Typical phosphites, used in most flexible PVC formulations, are sold for 4.00— 7.50/kg. Typical antioxidants are bisphenol A, selling at 2.00/kg Nnonylphenol at 1.25/kg and BHT at 3.50/kg, respectively. Pricing for ESO is about 2.00— 2.50/kg. Polyols, such as pentaerythritol, used with the barium—cadmium systems, sells at 2.00, whereas the derivative dipentaerythritol costs over three times as much. The P-diketones and specialized dihydropyridines, which are powerful costabilizers for calcium—zinc and barium—zinc systems, are very cosdy. These additives are 10.00 and 20.00/kg, respectively, contributing significantly to the overall stabilizer costs. Hydrotalcites are sold for about 5.00— 7.00/kg. [Pg.551]

Dendritic molecules with electroactive units at either the focal point or core have been reported [92, 97]. There are, however, only a few examples of such moieties specifically pinned within cascade infrastructure. Our recent efforts in this direction [104-106] involve the incorporation of chromophoric 1,4-di-aminoanthraquinone (35) within the cascade infrastructure. Dendrimers based on a four-directional pentaerythritol core were synthesized using the extended 1 — 3 building block 36. A high dilution technique was applied to synthesize 36... [Pg.50]

Four Ru(tpy) + units with or without carborane-type substituents have been linked to a pentaerythritol core. The resulting compounds exhibit only one cyclic voltammetric wave assigned to the simultaneous oxidation of the four metal-based centers [33]. [Pg.214]

Polyacetal resins have a repeating unit of -O-CH2-. They are strong, stiff polymers for valves, hoses, and tube connectors. Pentaerythritol finds end-uses in alkyd resins and explosives (pentaerythritol tetranitrate). To appreciate this synthesis, the student should review two condensation reactions, the crossed aldol and the crossed Cannizzaro. Acetaldehyde reacts with 3 mol of formaldehyde in three successive aldol condensations. This product then undergoes a Cannizzaro reaction with formaldehyde. [Pg.210]

You are a member of a firm doing consulting work on chemical engineering design The G. I. Treyz Chemical Company of Codes Falls, NY, has asked your firm to determine the advisability of adding a pentaerythritol production unit to its present formaldehyde plant. You have been sent to Cooks Falls to analyze the situation and obtain the necessary details. [Pg.846]

Complementary dendritic hexamers based on a central scaffold made up of linked pentaerythritol and tri(hydroxymethyl)amino methane units have been found to also exhibit liquid-crystalline properties. This star-shaped scaffold was used to create supermolecules containing two different hemispheres, referred to thereafter as Janus supermolecular Hquid crystals (Fig. 76) [323,324]. One of the hemisphere contains three cyanobiphenyl end-groups, whereas the other lobe consists of three chiral phenyl benzoate mesogenic moieties laterally attached. The type of mesophase observed (N ... [Pg.135]

Carbomer polymers are formed from repeating units of acrylic acid. The monomer unit is shown above. The polymer chains are crosslinked with allyl sucrose or allyl pentaerythritol. See also Section 4. [Pg.111]

The complementary materials 52 and 53, based on a central scaffold made up of pentaerythritol and tris(hydroxymethyl)aminomethane units linked together, where one unit carries three cyanobiphenyl (CB) (smectic preferring), see Fig. 61, and the other three chiral phenyl benzoate (PB) (chiral nematic preferring) mesogenic moieties, see Fig. 62, or vice-versa were investigated [115], see Fig. 63. [Pg.51]

United States Pentaerythritol tetranitrate, petrin, tetranitropentaerythritol, pen-taerythrite tetranitrate, penta, niperyth, nyperite, pentyl. [Pg.24]

Fig. 14.06. Plan of one layer of the tetragonal structure of pentaerythritol, C(CH2OH)4, projected on a plane perpendicular to the z axis. The heights of the atoms in one molecule are indicated in units of cj 100 and hydrogen bonds between hydroxyl groups are represented by broken lines. Fig. 14.06. Plan of one layer of the tetragonal structure of pentaerythritol, C(CH2OH)4, projected on a plane perpendicular to the z axis. The heights of the atoms in one molecule are indicated in units of cj 100 and hydrogen bonds between hydroxyl groups are represented by broken lines.
This strategy, and the ready availability of acrylate esters allows the straightforward synthesis of assemblies of multiple polyoxometalate units. Thus the composite star anion 11 was synthesized starting with pentaerythritol-tetraacrylate, the formation of C(CH20C0CH2CH2GeCl3)4, and subsequent reaction with [SiWn03t)] . ... [Pg.24]


See other pages where Pentaerythritol unit is mentioned: [Pg.38]    [Pg.9]    [Pg.38]    [Pg.9]    [Pg.292]    [Pg.55]    [Pg.232]    [Pg.751]    [Pg.55]    [Pg.320]    [Pg.751]    [Pg.219]    [Pg.36]    [Pg.236]    [Pg.399]    [Pg.442]    [Pg.9]    [Pg.307]    [Pg.31]    [Pg.338]    [Pg.21]    [Pg.240]    [Pg.253]    [Pg.359]    [Pg.359]    [Pg.115]    [Pg.200]    [Pg.391]    [Pg.52]    [Pg.363]    [Pg.340]   
See also in sourсe #XX -- [ Pg.38 ]




SEARCH



Pentaerythritol

© 2024 chempedia.info