Light color

The economics of recycling PET are more favorable than recycling HDPE. To iacrease the recycling of HDPE, the separation of bottles made of these two plastics could be omitted and a mixture processed. Coarse, light-colored powders of the two polymers have been prepared by an experimental soHd state shear extmsion pulverization process (55). The powder has been successfully injection molded without pelletization. 

A group of aminoxanthenes, ie, pyra2oloxanthenes, is used as color formers ia pressure or heat-sensitive imaging papers (43). These compounds are colorless, but, upon contact with acidic electron-accepting material, are converted to resonance forms that are lightly colored. An example is stmcture [58294-05-6] (35), which forms upon the condensation of A[,A/-diethyl-y -aminophenol with phthalic anhydride, followed by addition of 6-hydroxyinda2ole ia 80% sulfuric acid (44). 

Phormium. The Phormium tenax plant yields a long, light-colored, hard fiber also known as New Zealand hemp or flax, although it has none of the bast fiber characteristics. The plant is a perennial of the Agavaceae with leaves up to 4 m long and 10 cm wide. The fibers are recovered by mechanical decortication. 

Solvent extraction removes chlorophyll and other pigments to give a light-colored product but increases processing costs. Furthermore, solvent extraction removes p-carotene and reduces vitamin A activity (89) (see Terpenoids Vitamins). Supercritical CO2 extraction at 30 and 70 MPa (4,350 and 10,150 psi) and 40°C removed 90 and 70% carotene and lutein, respectively, from alfalfa LPC (96). This process avoids organic solvent residues and recovers valuable by-products. 

With the improvement of refining and purification techniques, many pure olefinic monomers are available for polymerization. Under Lewis acid polymerization, such as with boron trifluoride, very light colored resins are routinely produced. These resins are based on monomers such as styrene, a-methylstryene, and vinyltoluene (mixed meta- and i ra-methylstyrene). More recently, purified i ra-methylstyrene has become commercially available and is used in resin synthesis. Low molecular weight thermoplastic resins produced from pure styrene have been available since the mid-1940s resins obtained from substituted styrenes are more recent. 

Boron tritiuoride etherate— -hexanol complexes have successfully been used to polymerize P-pinene, as well as dipentene, to yield resins with softening points >70° C (82). Limonene or dipentene sulfate has been polymerized with aluminum chloride in a mixed toluene/high boiling aUphatic naphtha to give high yields of light colored resins (96). For the polymerization of dipentene or limonene, 4—8 wt % of AlCl has been used. Polymerization of P-pinene typically requires lower levels of catalyst relative to limonene or dipentene. 

The hard rock deposits are mined mainly for feldspar with mica and quartz being accessory minerals. These deposits are extensive, often covering hundreds of square meters and are recognized by the light-colored, granite-like appearance with shiny mica flakes being a prominent feature. The mica content of these deposits ranges from approximately 6—10 wt %. 

The slime, consisting of kaolin, fine quart2, and feldspar, is sometimes used as is after being dewatered. This material may be used in the manufacture of light-colored brick or may be further processed to produce a high grade ceramic kaolin used in the manufacture of dinnerware, electrical porcelain, or sanitary-ware (see Ceramics). Floes of kaolin may be sold in bulk from the drier or pulveri2ed and sold in a powdered form. 

Oleoresin. Natural oleoresins are exudates from plants, whereas prepared oleoresins are solvent extracts of botanicals, which contain oil (both volatile and, sometimes, fixed), and the resinous matter of the plant. Natural oleoresins are usually clear, viscous, and light-colored Hquids, whereas prepared oleoresins are heterogeneous masses of dark color. 

When petroleum occurs in a reservoir that allows the cmde material to be recovered by pumping operations as a free-flowing dark-to-light colored hquid, it is often referred to as conventional petroleum. In some oil fields, the downhole pressure is sufficient for recovery without the need for pumping. Heavy oil differs from conventional petroleum in that its flow properties are reduced and it is much more difficult to recover from the subsurface reservoir. These materials have a much higher viscosity and lower API (American Petroleum Institute) gravity than conventional petroleum, and primary recovery of these petroleum types usually requires thermal stimulation of the reservoir. 

BP. These nitrile alloy membranes are compounded from PVC, flexibilized by the addition of butadiene—acrylonitrile copolymers, PVC, and other proprietary ingredients. Typically reinforced with polyester scrim, NBP membranes are 1 mm thick and have a width of 1.5 m. They ate ptedominandy used in mechanically fastened roofing systems. NBP membranes exhibit excellent teat and puncture resistance as well as good weatherabihty, and remain flexible at low temperatures. They ate resistant to most chemicals but ate sensitive to aromatic hydrocarbons. The sheet is usually offered in light colors. The physical characteristics of NBP membranes have been described (15). 

In general, the amines are more active than the phenoHcs which are in turn more active than the phosphites. Amine antioxidants, however, often cause staining problems and are therefore used mainly in black stocks. The phenoHcs and phosphites are relatively nonstaining and are normally used ia light-colored mbbers. 

Raw juice is heated, treated sequentially with lime (CaO) and carbon dioxide, and filtered. This accomplishes three objectives (/) microbial activity is terminated (2) the thin juice produced is clear and only lightly colored and (J) the juice is chemically stabilized so that subsequent processing steps of evaporation and crystalliza tion do not result in uncontrolled hydrolysis of sucrose, scaling of heating surfaces, or coprecipitation of material other than sucrose. 

Specifically MSA has been found to be more effective than -toluenesulfonic acid and sulfuric acid in preparing dioctyl phthalate (405). A U.S. patent also discloses its use to prepare light-colored fatty esters (406). It is also important as a catalyst to prepare acrylates, methacrylates, adipates, phthalates, trimeUitates, thioglycolates, and other esters. 

The principal objection to -PDA antiozonants is their staining characteristics. The lack of suitable alternative antiozonants for light-colored diene mbber articles is one of the outstanding problems in mbber technology. Pew chemical antiozonants outside the class of -PDAs have much commercial importance. One of the few exceptions to this rule is 6-ethoxy-l,2-dihydro-2,2,4-trimethylquinoline [91-53-2] one of the first commercial antiozonants. 

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