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Infusions

Crude lead contains traces of a number of metals. The desilvering of lead is considered later under silver (Chapter 14). Other metallic impurities are removed by remelting under controlled conditions when arsenic and antimony form a scum of lead(II) arsenate and antimonate on the surface while copper forms an infusible alloy which also takes up any sulphur, and also appears on the surface. The removal of bismuth, a valuable by-product, from lead is accomplished by making the crude lead the anode in an electrolytic bath consisting of a solution of lead in fluorosilicic acid. Gelatin is added so that a smooth coherent deposit of lead is obtained on the pure lead cathode when the current is passed. The impurities here (i.e. all other metals) form a sludge in the electrolytic bath and are not deposited on the cathode. [Pg.168]

When silica is fused,. silica glass is formed. This has advantages over ordinary glass in that it is much less easily fused (it softens at about 1800 K). and has a very low coefficient of expansion. It is. therefore, used for crucibles and other articles required to be infusible... [Pg.186]

Sodium benzoate,—Burns with great difficulty, and after prolonged heating leaves a white infusible residue of NajCOj. Scrape this residue into a test-tube, and test for carbonate in the usual way. Typical of alkali salts of carboxylic acids. [Pg.319]

These are all empirical measurements, so the model of the harmonic oscillator, which is pur ely theoretical, becomes semiempirical when experimental information is put into it to see how it compares with molecular vibration as determined spectroscopically. In what follows, we shall refer to empirical molecular models such as MM, which draw heavily on empirical information, ab initio molecular models such as advanced MO calculations, which one strives to derive purely from theory without any infusion of empirical data, and semiempirical models such as PM3, which are in between (see later chapters). [Pg.97]

The various basis sets used in a calculation of the H and S integrals for a system are attempts to obtain a basis set that is as close as possible to a complete set but to stay within practical limits set by the speed and memory of contemporary computers. One immediately notices that the enterprise is directly dependent on the capabilities of available computers, which have become more powerful over the past several decades. The size and complexity of basis sets in common use have increased accordingly. Whatever basis set we choose, however, we are attempting to strike a balance. If the basis set is too small, it is inaeeurate if it is too large, it exceeds the capabilities of our computer. Whether our basis set is large or small, if we attempt to calculate all the H and S integrals in the secular matrix without any infusion of empirical information, the procedure is described as ab initio. [Pg.242]

These are relatively infusible, brittle materials that are insoluble in most solvents. [Pg.1019]

The reaction conditions can be varied so that only one of those monomers is formed. 1-Hydroxy-methylurea and l,3-bis(hydroxymethyl)urea condense in the presence of an acid catalyst to produce urea formaldehyde resins. A wide variety of resins can be obtained by careful selection of the pH, reaction temperature, reactant ratio, amino monomer, and degree of polymerization. If the reaction is carried far enough, an infusible polymer network is produced. [Pg.1025]

Some commercially important cross-linked polymers go virtually without names. These are heavily and randomly cross-linked polymers which are insoluble and infusible and therefore widely used in the manufacture of such molded items as automobile and household appliance parts. These materials are called resins and, at best, are named by specifying the monomers which go into their production. Often even this information is sketchy. Examples of this situation are provided by phenol-formaldehyde and urea-formaldehyde resins, for which typical structures are given by structures [IV] and [V], respectively ... [Pg.22]

This polymerization is carried out in the two stages indicated above precisely because of the insolubility and infusibility of the final product. The first-stage polyamide, structure [IX], is prepared in polar solvents and at relatively low temperatures, say, 70°C or less. The intermediate is then introduced to the intended application-for example, a coating or lamination-then the second-stage cyclization is carried out at temperatures in the range 150-300°C. Note the formation of five-membered rings in the formation of the polyimide, structure [X], and also that the proportion of acid to amine groups is 2 1 for reaction (5.II). [Pg.335]

It is also possible for a single monomer to behave as both diene and dienophile. Heating diacetylene [XXII] produces an infusible material which may be rationalized as follows ... [Pg.338]

Infringement search Infusion botanical extract Infusion mashing Infusors Ingrain Blue 2 1 Ingrain dyes Inhalation anesthetics Inherent viscosity Inhibin... [Pg.513]

The presence of stable free radicals in the final polycondensate is supported by the observation that traces of (11) have a strong inhibiting effect on the thermal polymerization of a number of vinyl monomers. Radical polymerization was inhibited to a larger extent by a furfural resin than by typical polymerization inhibitors (34). Thermal degradative methods have been used to study the stmcture of furfural resinifted to an insoluble and infusible state, leading to proposed stmctural features (35). [Pg.77]

Flaking paint is treated by infusion of an adhesive in the areas where needed, followed by resetting the flakes on the substrate the softening of the paint needed to bend it back is effected through solvent action or heat. Losses can only be filled and inpainted. Inpainting may also be necessary when cracks become so wide as to seriously affect the visual appearance of the painting. [Pg.427]

Several commercial polyester fabrics are flame retarded using low levels of phosphoms additives that cause them to melt and drip more readily than fabrics without the flame retardant. This mechanism can be completely defeated by the presence of nonthermoplastic component such as infusible fibers, pigments, or by siUcone oils which can form pyrolysis products capable of impeding melt flow (27,28). [Pg.475]

Another group of natural flavoring ingredients comprises those obtained by extraction from certain plant products such as vanilla beans, Hcotice root, St. John s bread, orange and lemon peel, coffee, tea, kola nuts, catechu, cherry, elm bark, cocoa nibs, and gentian root. These products are used in the form of alcohohc infusions or tinctures, as concentrations in alcohol, or alcohol—water extractions termed fluid or soHd extracts. Official methods for their preparation and specifications for all products used in pharmaceuticals are described (54,55). There are many flavor extracts for food use for which no official standards exist the properties of these are solely based on suitabiUty for commercial appHcations (56). [Pg.13]

Synthesis and Properties. Several methods have been suggested to synthesize polyimides. The predominant one involves a two-step condensation reaction between aromatic diamines and aromatic dianhydrides in polar aprotic solvents (2,3). In the first step, a soluble, linear poly(amic acid) results, which in the second step undergoes cyclodehydration, leading to an insoluble and infusible PL Overall yields are generally only 70—80%. [Pg.530]

The two primary types of plastics, thermosets and thermoplastics, are made almost exclusively from hydrocarbon feedstocks. Thermosetting materials are those that harden during processing (usually during heating, as the name implies) such that in their final state they are substantially infusible and insoluble. Thermoplastics may be softened repeatedly by heat, and hardened again by cooling. [Pg.369]

The seminal discovery that transformed membrane separation from a laboratory to an industrial process was the development, in the early 1960s, of the Loeb-Sourirajan process for making defect-free, high flux, asymmetric reverse osmosis membranes (5). These membranes consist of an ultrathin, selective surface film on a microporous support, which provides the mechanical strength. The flux of the first Loeb-Sourirajan reverse osmosis membrane was 10 times higher than that of any membrane then avaUable and made reverse osmosis practical. The work of Loeb and Sourirajan, and the timely infusion of large sums of research doUars from the U.S. Department of Interior, Office of Saline Water (OSW), resulted in the commercialization of reverse osmosis (qv) and was a primary factor in the development of ultrafiltration (qv) and microfiltration. The development of electro dialysis was also aided by OSW funding. [Pg.60]

The development of injectable mictocapsules for deUvery of chemotherapy agents remains another active area of research. The ultimate goal is to achieve targeted deUvery of chemotherapy agents to specific sites in the body, ideaUy by injection of dmg-loaded mictocapsules that would seek out and destroy diseased ceUs. Intra-arterial infusion chemotherapy is a direct approach to targeted deUvery. The clinical appHcations of microspheres and mictocapsules in embolization and chemotherapy have been assessed (49) (see Chemotherapeutics, anticancer). [Pg.324]

Infusion. Infusion botanical extracts are tinctures that have been concentrated by either total or partial removal of the alcohol by distillation. [Pg.296]

Commercially available containers for use with parenteral products include single-dose ampuls that are heat sealed and opened by snapping at the point of least diameter, vials for multidose use, and botdes and pHable bags that are used for large volumes such as needed in intravenous infusions. Container size can vary from 1 mL to 1 L. Generally volumes up to 100 mL are available as ampuls or vials. [Pg.234]


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Adjuvant hepatic arterial infusion

Administration by Injection or Infusion

Adrenaline intravenous infusion

Alanine infusion

Alemtuzumab infusion reaction

Allogeneic stem cell infusion

Ambulatory infusion pump

Amino acid infusion

Ammonium acetate infusion

Amphotericin infusion rate

Amphotericin infusion-related reactions

Analyte infusion

Aqueous infusions, extraction

Arterial infusion therapy

Artery infusion, hepatic

Baccharis articulata as infusions

Baccharis gaudichaudiana as infusion

Baccharis multiflora as infusion

Background Infusion Rate

Background infusion

Bacterial contamination infusion fluid

Bicarbonate infusion

Bolus infusion studies

Brain, heart infusion broth

Brain/heart infusion

Bronchial artery infusion

Children infusion

Concentrated infusions

Concentrated infusions waters

Continuous Infusion versus Double Bolus

Continuous basal insulin infusion

Continuous infusion

Continuous intravenous infusion

Continuous intravenous infusion constant rate

Continuous intravenous infusion flow rate

Continuous intravenous infusion loading dose

Continuous intravenous infusion parameters

Continuous intravenous infusion state

Continuous intravenous infusion steady-state plasma concentration

Continuous subcutaneous infusion

Continuous subcutaneous insulin infusion

Continuous subcutaneous insulin infusion CSII)

Crystal growth double-infusion

Cyclic infusion

Devices pump infusion

Dextrans intravenous infusions

Digoxin intravenous infusion

Direct Infusion ESMS of Crude Cell extracts for High-Throughput Characterizations—Metabolic Fingerprinting and Footprinting

Direct infusion

Direct infusion mass spectrometry

Disposable controlled-release device for drug infusion

Donor lymphocyte infusion

Dopamine intravenous infusion

Dosage regimen infusion rate

Dose to the patient from a multiple intermittent infusion

Drug administration intravenous infusion

Drug concentration with intravenous infusion

Drug delivery devices infusion

Drug distribution , volume intravenous infusion rate

Drug infusion

Drug infusion, intravenous

Dry infusion

EKOS MicroLys US infusion catheter

Electrospray mass spectrum infused

Elimination half life post-infusion data

Elimination rate continuous intravenous infusion

Example determination of a multiple intermittent infusion dosing regimen for an aminoglycoside antibiotic

Explosives infusible

External infusion pumps

Fibrolase infusion

Flow and Cure Monitoring of Resin Infusion Processes

Flow rate, intravenous infusion

Fluid therapy infusion rates/volumes

Fructose infusion

Glucose blood levels after infusion

Glucose controlled insulin infusion

Glucose controlled insulin infusion system

Glucose infusion

Glucose infusion clamp study

Glucose infusion rate

Glucose insulin potassium infusion

Glucose response following infusion

Glyceryl trinitrate infusion

Hemoglobin infusion

Hydrochloric acid infusion

Hypertonic saline infusion test

Hypoglycaemia infusion

Hypoglycemia infusate

IPMC Assisted Infusion Micropumps

IV infusion

Infliximab Infusion rate

Infusaid implantable infusion pump

Infusate contamination

Infused oil

Infusible

Infusible

Infusible polymers

Infusible resins

Infusible white precipitate

Infusion Applied Science

Infusion Confusion

Infusion Subject

Infusion administration

Infusion apparatus

Infusion bags

Infusion buffer capacity

Infusion central venous catheters

Infusion conditions

Infusion control device

Infusion definition

Infusion devices

Infusion devices portable

Infusion devices, comparison

Infusion duration

Infusion duration concentration

Infusion fluids

Infusion gentamicin

Infusion labelling

Infusion mass spectrometry

Infusion mass spectrometry liquid chromatography

Infusion micropumps

Infusion molding

Infusion of hydrochloric acid

Infusion optimization

Infusion osmotic value

Infusion packaging

Infusion peripheral access devices

Infusion peripherally inserted central catheters

Infusion policy

Infusion port systems

Infusion process, chemical

Infusion processes

Infusion product formulation

Infusion pump for

Infusion pumps

Infusion pumps advantages

Infusion pumps disadvantages

Infusion pumps portable

Infusion pumps problems with

Infusion pumps stationary

Infusion pumps, insulin

Infusion pumps, insulin diabetic ketoacidosis

Infusion rate constant

Infusion rates

Infusion rates control

Infusion rates loading

Infusion rates renal impairment

Infusion rates true steady-state

Infusion reactions

Infusion reactions intravenous immunoglobulin

Infusion solutions and emulsions

Infusion systems

Infusion techniques

Infusion therapy

Infusion therapy limitations

Infusion therapy rationale

Infusion types

Infusion, description

Infusion-related events

Infusion-related events amphotericin

Infusion-related reaction

Infusion-related reactions concentrate

Infusions, analysis

Infusions, grades

Infusions, herb

Injectable infusions

Injectable products intravenous infusions

Injections intravenous infusions

Insulin infusion

Insulin infusion pump systems

Insulin therapy continuous subcutaneous infusion

Insulin therapy infusion

Intermittent intravenous infusions, multiple

Interstitial infusion, direct

Intra-arterial infusion

Intraarterial infusion

Intracerebroventricular drug infusion

Intralipid infusion

Intrapleural infusion

Intravenous Administration Infusion

Intravenous bolus administration intermittent infusions

Intravenous infusion loading bolus

Intravenous infusion pharmacokinetics

Intravenous infusion therapy

Intravenous infusions

Intravenous infusions additives

Intravenous infusions plastic containers

Intravenous infusions, dose volume/rates

Intravenous-infusion bags

Iron dextran total dose infusion

Knowledge-infused processes

Knowledge-infused resources

Lactate infusion

Large-volume parenterals infusions

Lidocaine infusion

Lipid Concentration in the Infusion Solution

Liver continuous intravenous infusion

Loop diuretics continuous infusion

Lower gastrointestinal infusion

Medications continuous infusion

Membrane-based infusion processing

Membrane-based infusion processing behaviour

Metabolism intravenous infusion

Method resin infusion

Miniature disposable infusion IPMC

Miniature disposable infusion IPMC micropumps

Morphine intraspinal infusion

Multiple intermittent infusions

Multiple intermittent infusions concentrations

Nanoelectrospray infusion

One-compartment open model for continuous intravenous infusion

Paclitaxel infusion, prolonged

Parenteral administration infusion systems

Parenteral formulations infusions, stability

Parenteral nutrition continuous infusions

Parenteral preparations infusions

Peppermint infusion

Pharmacokinetics infusion rate constant

Phenol-formaldehyde resins Infusible

Plasma drug concentration intravenous infusion rate

Poly infusion containers

Polyvinyl chloride infusion lines

Postcolumn infusion

Primed constant infusion

Primed constant infusion technique

Propofol infusion syndrome

Pulsed infusion

Pulsed infusion shotfiring

Pulsed infusion technique

Pumping mechanism, infusion pumps

RIM Infusion Technology

Rationale for Infusion Therapy

Renal impairment infusion rate adjustment

Resin film infusion

Resin film infusion (RFI)

Resin infusion

Resin infusion between double flexible

Resin infusion between double flexible tooling

Resin infusion liquid composite moulding

Resin infusion process steps

Resin infusion technology

Resin infusion under flexible tooling

Resin infusion under flexible tooling RIFT)

Resin-infusion processes

Rituximab infusion reactions

SCRIMP infusion molding process

Saline infusion

Saline solution infusion rate

Sampling blood following cessation of infusion

Sampling drug in body or blood during infusion

Seemann Composite Resin Infusion Molding Process (SCRIMP)

Seemann composite resin infusion

Seemann composite resin infusion molding, SCRIMP

Seemann composites resin infusion molding

Seemann composites resin infusion molding process

Semi-fusible and infusible explosives

Shotgun Lipidomics Direct Infusion-Based Approaches

Single-Crystal Growth by a Double-Infusion Technique

Solvent infusions

Stationary and Portable Infusion Pumps

Stem cells intracoronary infusion

Subcutaneous drugs intravenous infusion rate

Summary of membrane-based infusion processing

Syringe infusion system

Systemic clearance intravenous infusion

Taurocholate infusion

Textbooks infusing green chemistry into

The Double-Infusion Technique

Thermal infusion

Thrombolytic infusion

Tissue plasminogen activator infusion

Trastuzumab infusion-related reactions

Turnover of GABA by Infusion With Labeled Precursors

Vacuum Bag Resin Infusion

Vacuum assisted resin infusion

Vacuum assisted resin infusion VARI)

Vacuum infusion

Vacuum infusion process

Vacuum-assisted resin infusion moulding

Variables in the Infusion Solution

Vasopressin infusion

Water infusion blasting

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