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Blocks selection

B = B 4, 1,4-polybutadiene block Bj 2, 1,2-polybutadiene block B y, medium vinyl (35-60%) polybutadiene block) I, 1,4-polyisoprene block. Selective hydrogenation this block not hydrogenated. [Pg.168]

The rapid increase in the separation factors observed for the individual series of columns reflected not only the improvement in the intrinsic selectivities of the individual selectors but also the effect of increased loading with the most potent selector. Although the overall loading determined from nitrogen content remained virtually constant at about 0.7 mmol g for all CSPs, the fractional loading of each selector increased as the number of selectors in the mixture decreased. Thus, the whole method of building block selection and sublibrary synthesis can be also viewed as an amplification process. [Pg.89]

Another problem in validating targets for behavioral disorders related to neurotransmitter abnormalities is the interplay between several neurotransmitter systems in specific brain regions. For example, in the hippocampus, limbic, and nigral-striatal areas, functions connected by serotonin, norepinephrine, and dopamine are interconnected so that blocking selected receptor subtypes or changing synaptic levels of certain neurotransmitters may... [Pg.228]

Albuterol serotonin reuptake inhibitor A bronchodilator that blocks selective / -adrenergic receptor. [Pg.41]

Abstract This article reviews results from our group of the synthesis and characterization of diblock copolymer brushes. Results from the literature are also covered. We report a wide variety of diblock compositions and compare the miscibility of the two blocks with the tendency to rearrange in response to block-selective solvents. Also, we describe the types of polymerization methods that can be utilized to prepare diblock copolymer brushes. We have compared the molecular weight of free polymer and the polymer brush based on results from our laboratory and other research groups we have concluded that the molecular weight of the free polymer and that of degrafted polymer brushes is similar. [Pg.125]

Styrene) (PPFS), poly(heptadecafluorodecyl acrylate) (PHFA), poly(penta-fluoropropyl acrylate) (PPFA), or poly(trifluoroethyl acrylate) (PTFA) [53]. The block at the silicate interface was either PS or PMA. Treatment of the diblock systems with block-selective solvents produced predictable changes in water contact angles except for those diblock brushes based on PHFA. All of these systems were fully characterized by XPS, tensiometry, ellipsometry,... [Pg.143]

Yan X, Liu G, Hu J, Willson CG. Coaggregation of B-C and D-C diblock copolymers with H-bonding C blocks in block-selective solvents. Mactomolecules 2006 39 1906-1912. [Pg.102]

The main indication for an inhibition of a-adreno-ceptors is an increased blood pressure. Drugs like prazosine, doxazosine or terazosine block selectively O 1-adrenoceptors, resulting in a relaxation of resistance arteries, arteriols and venules. This subtype selectivity, leaving the Q 2-iiiediated autofeedback control unaltered, may be the cause for... [Pg.306]

The secretion of T4 and T3 requires the uptake of follicular contents across the follicular cell apical membrane, the enzymatic release of T4 and T3 from peptide linkage within Tg, and the transport of T4 and T3 across the follicular cell basal membrane to the blood. Several of the steps in synthesis and secretion of T4 and T3 may be compromised by iodine deficiency or disease and can be blocked selectively by a variety of chemicals and drugs. [Pg.743]

Norepinephrine is removed from the synapse by means of two mechanisms. In the hrst, catechol-O-methyl-transferase (COMT) degrades intrasynaptic NE. In the second, the norepinephrine transporter (NET), a Na /CH-dependent neurotransmitter transporter, is the primary way of removing NE from the synapse [(4) in Fig. 2.7]. The NET is blocked selectively by desipramine and nortriptyline. Once internalized. [Pg.28]

Dopamine is removed from the synapse via two mechanisms. First, COMT degrades intrasynaptic DA. Second, the dopamine transporter (DAT) [see (4) in Fig. 2.9], a Na /CD-dependent neurotransmitter transporter, transports DA in either direction, depending on the concentration gradient. The DAT is blocked selectively by drugs such as cocaine, amphetamine, bupropion, and nomifensine. [Pg.31]

To place a title block, select Place and then Title Block from the menus ... [Pg.49]

We can now start placing parts. We will have a top level drawing that only contains hierarchical blocks. We will first create these blocks. We will then descend into each block and create the specific circuit for that block. Select Place and then Hierarchical Block from the menus ... [Pg.77]

As an example of showing a hierarchical block within a hierarchical block, we will add a hierarchical block to this schematic. To place a block, select Place and then Hierarchical Block. To place a pin, select Place and then Hierarchical Pin. This block has three pins called Ollt-L, Out-R, and Ground. The reference is BLK4, and the name of the block is LOSd. The block is shown below. Use the techniques covered earlier to create this block ... [Pg.88]

Next, we will create the schematic inside this block. Select the block and then descend the hierarchy. You will create the new schematic page below ... [Pg.88]

The endothelin system can be blocked with receptor antagonists and drugs that block endothelin-converting enzyme. Endothelin or ETB receptors can be blocked selectively, or both can be blocked with nonselective - antagonists. [Pg.386]

The properties of all the blocks in the flowsheet must be set. Clicking on the + to the left of Blocks generates a list of all the blocks. Selecting the pump block PI opens the window shown in Figure 2.43. We specify a pressure increase of 5 atm. Selecting the valve V1 block opens the window shown in Figure 2.44. Since the reactor pressure is 10 atm, the outlet pressure of VI (the benzene feed) is specified at 10 atm. The valve V2 (the ethylene feed) is defined in the same way. The valve V3 is set to take a 3 atm pressure drop, as shown in Figure 2.45. [Pg.80]

The disturbance considered is a step increase in the flowrate of the ethylene feed. We want to increase the benzene feed whenever the ethylene feed is increased, so a ratio control structure is installed. Figure 3.89 shows a Mulitply block selected from the list of ControlModels, dropped on the flowsheet, and renamed ratio. A control signal is attached to the FE stream and connected to ratio.Inputl, as shown in the upper window of Figure 3.90. Another control signal is attached from the output of the multiply block to the setpoint of the benzene flow controller. Clicking the ratio icon, clicking the right... [Pg.182]

PU systems with hard blocks made of piperazine, have been also studied [90, 91, 92], In systems deuterated in the segments of the soft blocks, 2H NMR results show that a fraction of the soft segments have a restricted mobility, due to the connectivity to hard blocks, rather than to the adsorption on those blocks acting as filler particles [93]. To study the interface in a specific way, systems with hard blocks selectively deuterated at different positions have been synthetised. A reduction of quadrupolar interaction according to the position was observed, corresponding to an increase of the mobility in hard segments on approaching the hard-soft interface. [Pg.587]


See other pages where Blocks selection is mentioned: [Pg.72]    [Pg.481]    [Pg.982]    [Pg.46]    [Pg.225]    [Pg.164]    [Pg.55]    [Pg.106]    [Pg.206]    [Pg.78]    [Pg.12]    [Pg.137]    [Pg.140]    [Pg.145]    [Pg.192]    [Pg.612]    [Pg.5]    [Pg.112]    [Pg.369]    [Pg.56]    [Pg.199]    [Pg.101]    [Pg.13]    [Pg.66]    [Pg.412]    [Pg.40]    [Pg.157]   


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Beta-blocking drugs selectivity

Block site-selective complexation

Block site-selective doping

Block-selective solvent

Blocking groups selectively removable

Combinatorial chemistry building blocks selection

Electrochemical Polarization—The Effect of Selectively Blocking Electrodes

Electrode blocking, selectively

Mesophase Morphologies of Silicone Block Copolymers in a Selective Solvent Studied by SAXS

Selecting a Block of Cells

Selecting a Different Title Block

Selection of building blocks

Selective blocking

Selective blocking

Self-assembly in Block-selective Solvents

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