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Proprietary

CaC3Hs(0H)2p04,H20. A constituent of many proprietary nerve tonics. [Pg.76]

On the other hand, the NDT service business has evolved towards a more open market, in which the prime contractor requires a transparent access to the data provided by the supplier, in order to ensure the comparison of data obtained from different sources and at different periods of time. Existing fomiats are most of the time proprietary formats released by instrument manufacturers, generally dealing with a unique NDT method and not including complementary information on the acquisition consequently, they fail to meet these requirements. [Pg.922]

Given the enormous number of resources for chemical information available, many researchers do not have the time to learn the details of the variotis systems, and they end up searching in only a few resources with which they are familiar. This is a dangerous approach Knowing that both fee and non-fee resources are available on the Internet and both hold the desired information, it is prudent to search non-fee systems first and then use proprietary databases to fill data gaps [49]. [Pg.271]

The similarity of the retrieved protons to those of the query structure, and the distribution of chemical shifts among protons with the same HOSE codes, can be used as measures of prediction reliability. When common substructures cannot be found for a given proton (within a predefined number of bond spheres) interpolations are applied to obtain a prediction proprietary methods are often used in commercial programs. [Pg.522]

The HyperChem philosophy associated with back end computations is one which is in tended to in still eon fiden ce. as far as is possible. in the scientific results emanating from HyperChem. This ph ilosoph y is on e of open n ess — open n ess aboii t the prod net. the calculations being performed, the science embodied in the product, etc. Apart from protecting the proprietary code associated with a commercial product. Hypercube wushes to document and describe as fully as is possible tb e calculation s th at HypcrCb cm performs. There should be no mystery about the scientific results obtained with HyperChem. [Pg.157]

ChemSketch has some special-purpose building functions. The peptide builder creates a line structure from the protein sequence defined with the typical three-letter abbreviations. The carbohydrate builder creates a structure from a text string description of the molecule. The nucleic acid builder creates a structure from the typical one-letter abbreviations. There is a function to clean up the shape of the structure (i.e., make bond lengths equivalent). There is also a three-dimensional optimization routine, which uses a proprietary modification of the CHARMM force field. It is possible to set the molecule line drawing mode to obey the conventions of several different publishers. [Pg.326]

Uses. Furfural is primarily a chemical feedstock for a number of monomeric compounds and resins. One route produces furan by decarbonylation. Tetrahydrofuran is derived from furan by hydrogenation. Polytetramethylene ether glycol [25190-06-1] is manufactured from tetrahydrofuran by a ring opening polymeri2ation reaction. Another route (hydrogenation) produces furfuryl alcohol, tetrahydrofurfuryl alcohol, 2-methylfuran, and 2-methyltetrahydrofuran. A variety of proprietary synthetic resins are manufactured from furfural and/or furfuryl alcohol. Other... [Pg.78]

After image transfer, the patterned resist must be readily and completely removable without substrate damage. The pattern often can be stripped from the substrate with a mild organic solvent. Proprietary stripper formulations or plasma oxidation treatments are utilized when the imaging chemistry or image transfer process has iasolubilized the pattern. [Pg.114]

Note for Guidance on Plasma Derived Mediciaal Products," CPMP/BWP/269/95, Committee for Proprietary Mediciaal Products (CPMP), London, Mar. 13, 1996. [Pg.145]

Glycolysis is claimed to be somewhat less cosdy than methan olysis (33). Depolymerization is not taken completely to monomers (34). Rather, recovered PET is depolymerized to low molecular weight oligomers. Contaminants are removed using proprietary technology. The oligomers are then fed to a melt polymerization vessel in which PET is produced. [Pg.230]

Sweet. California (etc) red table and sweet red table, proprietary types generally without specific fmit or varietal aroma unless Concord-type or fmit wines (blackberry, raspberry, strawberry, etc)... [Pg.367]

B) Coolers, refreshment wines made from white or red wine according to a proprietary formula. Low alcohol, often because of blending with various fmit juices California Cooler brand and others. [Pg.367]

B) Proprietary types Mixed fmit-flavored (Thunderbkd, etc). See also category. A. >.d)... [Pg.368]

In 1997, UOP announced the PX-Plus process which also uses a selectivated catalyst to convert toluene to para-rich xylenes. Pina commercialized a TDP process known as the (T2PX) process in 1984 (70). It uses a proprietary catalyst to react toluene at 42—48% conversion with selectivities to benzene of 42 wt % and to xylenes of 46 wt %. The xylenes produced are at equiUbrium. Typical commercial operating conditions of 390—495°C, H2 partial pressure of 4.1 Mpa, H2/hydrocarbon molar ratio of 4 1, and LHSV of 1—2/h. Pina s first commercial implementation occurred in 1985 at their Port Arthur refinery. [Pg.417]

The Aromax process was developed in the early 1970s by Toray Industries, Inc. in Japan (95—98). The adsorption column consists of a horizontal series of independent chambers containing fixed beds of adsorbent. Instead of a rotary valve, a sequence of specially designed on—off valves under computer control is used to move inlet and withdrawal ports around the bed. Adsorption is carried out in the Hquid phase at 140°C, 785—980 kPA, and 5—13 L/h. PX yields per pass is reported to exceed 90% with a typical purity of 99.5%. The first Aromax unit was installed at Toray s Kawasaki plant in March 1973. In 1994, IFP introduced the Eluxyl adsorption process (59,99). The proprietary adsorbent used is designated SPX 3000. Individual on-off valves controlled by a microprocessor are used. Raman spectroscopy to used to measure concentration profiles in the column. A 10,000 t/yr demonstration plant was started and successfully operated at Chevron s Pascagoula plant from 1995—96. IFP has Hcensed two hybrid units. [Pg.420]

The reaction is very exothermic. The heat of reaction of propylene oxidation to acrolein is 340.8 kJ /mol (81.5 kcal/mol) the overall reactions generate approximately 837 kJ/mol (200 kcal/mol). The principal side reactions produce acryUc acid, acetaldehyde, acetic acid, carbon monoxide, and carbon dioxide. A variety of other aldehydes and acids are also formed in small amounts. Proprietary processes for acrolein manufacture have been described (25,26). [Pg.123]

The design and manufacture of adsorbents for specific appHcations involves manipulation of the stmcture and chemistry of the adsorbent to provide greater attractive forces for one molecule compared to another, or, by adjusting the size of the pores, to control access to the adsorbent surface on the basis of molecular size. Adsorbent manufacturers have developed many technologies for these manipulations, but they are considered proprietary and are not openly communicated. Nevertheless, the broad principles are weU known. [Pg.269]

Auckland Regional Authority converted two M.A.N. buses to use a cetane improver and methanol and South Africa investigated the use of methanol with a proprietary cetane improver. Eour Renault buses were converted in Tours, Erance to operate on ethanol and a cetane improver, Avocet, manufactured by Imperial Chemical Industries (ICI). The results of these demonstrations were also technically successfiil slightly better fuel economy was obtained on an energy basis and durabiUty issues were much less than the earlier tests using dedicated engines. [Pg.433]

Worldwide Technology Assessment of Nitroglycerin Manufacture, 4 Vols., (Proprietary Information) Mason and Hanger, Silas Mason, 1985. [Pg.27]

Recent advances in Eischer-Tropsch technology at Sasol include the demonstration of the slurry-bed Eischer-Tropsch process and the new generation Sasol Advanced Synthol (SAS) Reactor, which is a classical fluidized-bed reactor design. The slurry-bed reactor is considered a superior alternative to the Arge tubular fixed-bed reactor. Commercial implementation of a slurry-bed design requires development of efficient catalyst separation techniques. Sasol has developed proprietary technology that provides satisfactory separation of wax and soHd catalyst, and a commercial-scale reactor is being commissioned in the first half of 1993. [Pg.164]

The American Spice Trade Association (ASTA) (4) accepts spice as any dried plant product used primarily for seasoning purposes. This broad definition was designed so that items labeled only as spice could give adequate protection to proprietary formulas for spice mixtures. However, ASTA recommends that the dehydrated vegetables and the color spices be listed separately by name on all labels. ASTA also has recommended that the capsicums, no matter the species, be delisted as spices and labeled separately. [Pg.23]

Flow Nozzles. A flow nozzle is a constriction having an eUiptical or nearly eUiptical inlet section that blends into a cylindrical throat section as shown in Figure 8. Nozzle pressure differential is normally measured between taps located 1 pipe diameter upstream and 0.5 pipe diameters downstream of the nozzle inlet face. A nozzle has the approximate discharge coefficient of an equivalent venturi and the pressure drop of an equivalent orifice plate although venturi nozzles, which add a diffuser cone to proprietary nozzle shapes, are available to provide better pressure recovery. [Pg.60]

Many different processes using HF as a reactant or source of fluorine are employed in the manufacture of fluorinated chemical derivatives. In many cases the chemistry employed is complex and in some cases proprietary. Electrochemical fluorination techniques and gaseous fluorine derived from HF are used in some of these appHcations. [Pg.199]


See other pages where Proprietary is mentioned: [Pg.1024]    [Pg.45]    [Pg.607]    [Pg.658]    [Pg.351]    [Pg.975]    [Pg.45]    [Pg.82]    [Pg.89]    [Pg.143]    [Pg.367]    [Pg.367]    [Pg.368]    [Pg.368]    [Pg.374]    [Pg.392]    [Pg.67]    [Pg.186]    [Pg.525]    [Pg.283]    [Pg.297]    [Pg.489]    [Pg.491]    [Pg.125]    [Pg.127]    [Pg.146]    [Pg.418]   
See also in sourсe #XX -- [ Pg.609 ]

See also in sourсe #XX -- [ Pg.169 ]

See also in sourсe #XX -- [ Pg.169 ]




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ABEX Proprietary Surfactants for Emulsion Polymerization

Broken Hill Proprietary Company Ltd

CPMP (Committee for Proprietary Medicinal

Carbonate systems, proprietary

Chemical Databases Proprietary

Chemical peels proprietary

Chinese proprietary medicine

Committee for Proprietary

Committee for Proprietary Medicinal

Committee for Proprietary Medicinal Products

Committee for Proprietary Medicinal Products (CPMP

Committee on Proprietary Medicinal

Committee on Proprietary Medicinal Products

Committee on Proprietary Medicinal Products CPMP)

Corporate proprietary databases

Diazepam proprietary names

Document Management Systems Proprietary

European Committee for Proprietary

Exporting Other Proprietary Data Formats

Files in Other Proprietary Data Formats

International Non-Proprietary Name

International Proprietary Name

Our Proprietary Cell Design

Processor proprietary

Proprietary 3-D weaving processes

Proprietary Association of Great

Proprietary Association of Great Britain

Proprietary Chemical Information

Proprietary Chemical Information Databases

Proprietary Chemical Information Management

Proprietary Chemical Information Reactions

Proprietary Designs to Reduce Vibration

Proprietary Information Agreements

Proprietary Solvent Formulations

Proprietary Tools

Proprietary audit systems

Proprietary blend

Proprietary data formats

Proprietary databases

Proprietary drug names

Proprietary drug prescribing

Proprietary drugs

Proprietary equipment

Proprietary information, disclosure

Proprietary medicinal products

Proprietary medicinal products controls

Proprietary medicines

Proprietary name

Proprietary name confusion

Proprietary name formulation

Proprietary names index

Proprietary names protection

Proprietary networks

Proprietary nucleating agents

Proprietary peels

Proprietary processing aids

Proprietary screening methods

Proprietary software

Proprietary specifications

Proprietary technology

Proprietary trays

Proprietary valve tray design

Reactions Databases Proprietary

Return of Proprietary Documents

Substructures Proprietary

The Committee for Proprietary

The Committee for Proprietary Medicinal Products,

Validation with Proprietary Compounds

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