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Qaagi - Book of Why

Causes

Effects

to form hybrid layers that penetrate the collagen fiber and form bonding between dentine surface and cement [ 17(passive) is setThe monomer

The UV - curable resincomposedof the monomer

organic polymerscomposedof monomer

a polymer materialcomposedof monomer

a base polymercomposedof the monomer

the hydrophilic polymercomposedof the monomer

means of at least two molar equivalents of thiole to one molar equivalent of the basic substance(passive) is created byThe monomer

to use copolymercomposedof monomer

a photosetting or UVsettingmonomer

The latter , Kingdesignedthe monomer

to sonicated for 2 minutes at full powerto createmonomer miniemulsion

combining ethylene oxide ( EO ) and carbon monoxide ( CO ) in the COEth TM process(passive) created byThe monomer

to fine tune the BNA structure(passive) was designedThe monomer

The mixture ... 30 minutesto setthe monomer

of two major structural domains : a nucleotide - binding domain and a catalytic / multimerization domain(passive) is composedThe monomer

A device according to claim 1 , whereby the polyfunctional acrylic monomer comprises at least one pHsettingmonomer

The second resin layer 130may preventthe monomer

of one to many atoms which form the base unit which is repeated to form a polymer , as represented in the figure below(passive) can be composedA monomer

For example , after synthesizing an oligomer having two or more repeating units , polymerizing active groups may be introduced into the oligomerto createa monomer

to provide a strong donor - acceptor interaction and high solubility for the corresponding polymer(passive) is designedThe monomer

Examples of polymer which has amino group on side chain ... whose polymer chainis ... composedof monomer

extensively modifying the structure of tetrathiafulvalene , a heterocyclic compound containing four sulphur atoms(passive) was created byThe monomer

the effect of the photo reaction initiator when the initiator is irradiated by UV rays(passive) caused bythe monomer

scientists at Dow Chemical Company and results from polymerizing a mixture of sodium acrylate and acrylic acid(passive) was invented bymonomer

A barrier 24 between the lamp and the monomer reservoir 16 and a baffle 26 attached to the housing of UV lamp 22preventedthe monomer

of ethyl methacrylate , a catalyst to speed up the initiator in the powder , inhibitors that keep the monomer from hardening before being mixed with powder , UV absorbers to prevent the nails from yellowing , and wetting agents(passive) is composedA monomer

base monomers base monomerssetof Monomer

The amount of the structural unit ( b2 - 4 )composedof the monomer

a homopolymercomposedof the monomer

of a first monomer and other monomer(passive) is composedpolymerizable monomer

at least one hydrogen atomcomposinga monomer

the sterilization process(passive) caused bythe monomer

to begin polymerization and crosslinking(passive) is causedThe monomer

application of energy(passive) set bythe monomer

even up to millions of times then ... all the molecules acting togethercreatesa monomer

at least one carbonylcontributingmonomer

This inhibiting agentshould preventthe monomer

the steps of initiating solution or suspension copolymerization of maleic acid anhydride and diisobutylene ... maintainingresultingmonomer

Concentrated solutionscomposedof the monomer

76 - Noble C , Dong J , Manser E , Song H. BCL - XL and UVRAGcausea monomer

mainly of acrylonitrilecomposedmainly of acrylonitrile

oleophobic properties to the polymercontributesoleophobic properties to the polymer

oleophobic properties to the ( co)polymer . 31contributesoleophobic properties to the ( co)polymer . 31

oleophobic properties to the ( co)polymer . 29contributesoleophobic properties to the ( co)polymer . 29

oleophobic properties to the ( co)polymer . 32contributesoleophobic properties to the ( co)polymer . 32

oleophobic properties to the ( co)polymer . 30contributesoleophobic properties to the ( co)polymer . 30

oleophobic properties to the ( co)polymer . 42contributesoleophobic properties to the ( co)polymer . 42

oleophobic properties to the ( co)polymer . 40contributesoleophobic properties to the ( co)polymer . 40

mainly of an ethylenically unsaturated compound in the presence of the polymer particle ( Icomposedmainly of an ethylenically unsaturated compound in the presence of the polymer particle ( I

of acrylic acid ( acrylatecomposed primarilyof acrylic acid ( acrylate

forth in either of claim 1 or 3 as a polymerization componentsetforth in either of claim 1 or 3 as a polymerization component

forth in claim 3 whereinsetforth in claim 3 wherein

forth in claim 6 whereinsetforth in claim 6 wherein

mainly of methyl methacrylate or diethyienecomposedmainly of methyl methacrylate or diethyiene

forth in claim 1 wherein the said physicochemically operative moieties are diaminessetforth in claim 1 wherein the said physicochemically operative moieties are diamines

to the polar segment of said polymer materialcontributingto the polar segment of said polymer material

mainly of styrene or a mixture of styrene and acrylonitrilecomposedmainly of styrene or a mixture of styrene and acrylonitrile

mainly of alkyl acrylate monomercomposedmainly of alkyl acrylate monomer

forth in claim 7setforth in claim 7

in the polymer unsaturationresultingin the polymer unsaturation

a condensed polymercomposinga condensed polymer

a vinyl polymercomposinga vinyl polymer

mainly of a specific methacrylate estercomposedmainly of a specific methacrylate ester

mainly of the aromatic vinyl compound and the monomer composed mainly of the methacrylic estercomposedmainly of the aromatic vinyl compound and the monomer composed mainly of the methacrylic ester

metal - chelating functionalitycontributesmetal - chelating functionality

mainly of methyl methacrylate in the presence of a partially hydrogenated conjugated diene polymercomposedmainly of methyl methacrylate in the presence of a partially hydrogenated conjugated diene polymer

mainly of methyl methacrylate having Tg of 25 ° C. or higher , ( IIcomposedmainly of methyl methacrylate having Tg of 25 ° C. or higher , ( II

the second network structure in relation to compression stress and strain at rupture in a 1PAMPS4-XPAAm0.1 DN gel , wherein the second monomer concentration along the abscissarefers to the concentration of the second monomer used for polymerization , to which X in " 1PAMPS - XPAAm0.1 " correspondscomposingthe second network structure in relation to compression stress and strain at rupture in a 1PAMPS4-XPAAm0.1 DN gel , wherein the second monomer concentration along the abscissarefers to the concentration of the second monomer used for polymerization , to which X in " 1PAMPS - XPAAm0.1 " corresponds

forth in claim 2 whereinsetforth in claim 2 wherein

forth in claim 8 whereinsetforth in claim 8 wherein

forth in claim 5 whereinsetforth in claim 5 wherein

forth in claim 4 whereinsetforth in claim 4 wherein

the second network structure in relation to compression stress and strain at rupture in a 1PAMPS4-XPAAm0.1 DN gel , wherein the second monomer concentration along the horizontal axis refers to the concentration of the second monomer used for polymerization , to which X in “ 1PAMPS - XPAAm0.1 ” correspondscomposingthe second network structure in relation to compression stress and strain at rupture in a 1PAMPS4-XPAAm0.1 DN gel , wherein the second monomer concentration along the horizontal axis refers to the concentration of the second monomer used for polymerization , to which X in “ 1PAMPS - XPAAm0.1 ” corresponds

from a C9 fraction ( or more generally from a C8 a C10 fractionresultingfrom a C9 fraction ( or more generally from a C8 a C10 fraction

of methyl methacrylate and styrenecomposedof methyl methacrylate and styrene

to the polymerised chain such as defined above in the presence of a chain transfer agent constituted by glutathioneleadingto the polymerised chain such as defined above in the presence of a chain transfer agent constituted by glutathione

of propylene , intrinsic viscositymainly composedof propylene , intrinsic viscosity

to the polymerised chain in the presence of a chain transfer agent constituted of glutathioneleadingto the polymerised chain in the presence of a chain transfer agent constituted of glutathione

to the basic nature of the polymer , or as a non - base if the monomer does not contribute to the basic nature of the polymercontributesto the basic nature of the polymer , or as a non - base if the monomer does not contribute to the basic nature of the polymer

to polymer B. 8leadsto polymer B. 8

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Smart Reasoning:

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