ライフサイエンスコーパス: methyl methacrylate

1 (n = 2) designs; all CTRs were made of poly(methyl methacrylate).

2 isted micromolding of nanostructures in poly(methyl methacrylate).

3 ,4-butadiene), poly(-caprolactone), and poly(methyl methacrylate).

4 ting multilayer microfluidic devices in poly(methyl methacrylate).

5 ar isotactic-b-syndiotactic stereoblock poly(methyl methacrylate).

6 act with fused silica, polystyrene, and poly(methyl methacrylate).

7 actured onto a disk-shaped substrate of poly(methyl methacrylate).

8 oly(4-methylstyrene) and polyethylene-g-poly(methyl methacrylate).

9 lyethylene, ethylene vinyl acetate, and poly(methyl methacrylate).

10 irect the assembly of polystyrene-block-poly(methyl methacrylate).

11 hill or plateau regions were primarily poly(methyl methacrylate).

12 active deformation of a polymer glass [poly(methyl methacrylate)].

13 oxide and 2a catalyzes the polymerization of methyl methacrylate.

14 ithin sections of material embedded in butyl-methyl-methacrylate.

15 d using a plastic microbead suspension (poly(methyl methacrylate) (5-27 mum), polyethylene (10-27 mum

16 Two-step syntheses of "Roche" ester from methyl methacrylate (79%; er 99:1), arguably the most wi

17 channels composed of a single material, poly(methyl methacrylate) (acrylic) or poly(dimethylsiloxane)

18 h-glass transition temperature polymer, poly(methyl methacrylate), adsorbed on nanoparticles and a lo

19 otoreactions: (1) the photopolymerization of methyl methacrylate and (2) photocatalyzed alkyne insert

20 This new derivative was copolymerized with methyl methacrylate and decyl methacrylate (MMA-DMA) to

21 II), were synthesized and copolymerized with methyl methacrylate and decyl methacrylate.

22 ased monomers and the photopolymerization of methyl methacrylate and made it possible to determine th

23 ed multiblock copolymer based on fatty acid, methyl methacrylate and PHB was first time synthesized.

24 n cycles are demonstrated in copolymers with methyl methacrylate and styrene without escalation in di

25 The monomer scope is extended to include methyl methacrylate and styrene.

26 synthesis of the chloroform-compatible poly(methyl methacrylate) and dimethyl sulfoxide (DMSO)-compa

27 -functionalized polymers with isotactic poly(methyl methacrylate) and fullerene C60 generates supramo

28 th slowly polymerizing monomers (styrene and methyl methacrylate) and initiators that were generated

29 osed of alternating layers of patterned poly(methyl methacrylate) and nanocapillary array membranes c

30 t (UV)-photomodification protocol using poly(methyl methacrylate) and polycarbonate to produce functi

31 g MP L(-1)), mainly TWP and clusters of poly(methyl methacrylate) and polyethylene terephthalate occu

32 tra was evaluated on reference samples [poly(methyl methacrylate) and silica].

33 d unzipping of both conventional (e.g., poly(methyl methacrylate)) and bulky (e.g., poly(oligo(ethyle

34 yrene, polyethylene, polypropylene, and poly(methyl methacrylate)) and confirm their localization in

35 Grafts consisting of polystyrene, poly(methyl methacrylate), and poly(2-hydroxyethyl)methacryla

36 ces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl methacrylate), poly

37 assy polystyrene, poly(vinyl chloride), poly(methyl methacrylate), and poly(ethylene terephthalate) e

38 e terephthalate), poly(vinyl chloride), poly(methyl methacrylate), and polycarbonate are proposed for

39 a bulk polymerization of N-vinylpyrrolidone, methyl methacrylate, and a diphenylamine-functionalized

40 , anesthetic gases, chemotherapy agents, and methyl methacrylate; and psychological stress and discri

41 ulk polymerization using methacrylic acid or methyl methacrylate as monomer and ethylene glycol dimet

42 step in the commercial (Alpha) production of methyl methacrylate as well as very high selectivity to

43 acrylate (PEGA480), tert-butyl acrylate, and methyl methacrylate, as well as styrene.

44 r materials that are amphiphilic (e.g., poly(methyl methacrylate)-b-poly(N,N-dimethylacrylamide)) and

45 de)) and/or mechanically diverse (e.g., poly(methyl methacrylate)-b-poly(N,N-dimethylaminoethylmethac

46 Obtained 40-nm poly(methyl methacrylate)-based NP probe, encapsulating octad

47 Recently, a new class of synthetic methyl methacrylate-based random heteropolymers (MMA-bas

48 h superior mechanical properties to those of methyl methacrylate-based TPEs.

49 copolymer, consisting of a hydrophobic poly(methyl methacrylate) block and a hydrophilic poly[N,N-2-

50 copolymers based on poly(methacrylic acid-co-methyl methacrylate)-block-poly(ethylene glycol).

51 ployed in the gel was polystyrene-block-poly(methyl methacrylate)-block-polystyrene, where the solvop

52 copolymers of poly(methyl acrylate) and poly(methyl methacrylate) blocks were investigated.

53 Butyl-Methyl Methacrylate (BMMA) plastic was adopted as it pre

54 tated the synthesis of densely tethered poly(methyl methacrylate) brush oNPs.

55 The reactors were fabricated in poly(methyl methacrylate) by hot embossing using a mold maste

56 We synthesized poly(methyl acrylate-b-methyl methacrylate) by PET-RAFT using fac-Ir(ppy)(3), a

57 used as a detector on an r = 8 mum bore poly(methyl methacrylate) capillary in a split effluent strea

58 re, TWP prevailed in the SML, while the poly(methyl methacrylate) cluster dominated the ULW.

59 moiety (AU-1) and covalently grafted into a methyl methacrylate-co-decyl methacrylate polymer matrix

60 nm) are blended with a THF solution of poly(methyl methacrylate-co-decyl methacrylate), poly(n-butyl

61 pper layer of the pH responsive polymer poly(methyl methacrylate-co-methacrylic acid) (Eudragit S100(

62 proximately 80% coisotactic poly[styrene-co-(methyl methacrylate)] (coiso-PSMMA) which contains appro

63 those for single-walled carbon nanotube-poly(methyl methacrylate) composites.

64 On silica (-SiOH) or poly(methyl methacrylate) (-COOH) surfaces, AEX latex attachm

65 acrylate poly(N-(methacryloxy)phthalimide-co-methyl methacrylate) copolymers with a degradation effic

66 sisting of DOTA chelators attached to a poly(methyl methacrylate) core and CANF-targeting moieties at

67 P-II) was conjugated to a biocompatible poly(methyl methacrylate)-core/polyethylene glycol-shell amph

68 ion and polymerization, a biocompatible poly(methyl methacrylate)-core/polyethylene glycol-shell amph

69 and those with a patch-like polystyrene/poly(methyl methacrylate) corona were prepared.

70 brought into contact with a deuterated poly(methyl methacrylate) (d-PMMA) film, and the interfacial

71 n measured between (a) the activated olefins methyl methacrylate-d(5) and styrene-d(8), and (b) the C

72 ane presented here is based on the copolymer methyl methacrylate-decyl methacrylate (MMA-DMA).

73 es were prepared by using a plasticizer-free methyl methacrylate-decyl methacrylate copolymer as memb

74 ce spatially defined sample patterns on poly(methyl methacrylate) discs.

75 icrobial fuel cell (see picture; PMMA = poly(methyl methacrylate), E = electrode).

76 noethyl methacrylate, butyl methacrylate and methyl methacrylate, E) to enhance vancomycin encapsulat

77 thod of band fitting, of the spectra of poly(methyl methacrylate) films deposited on gold, we demonst

78 Nile Red/poly(methyl methacrylate) films prepared for comparisons exhi

79 Poly(lactic acid) and poly(methyl methacrylate) films were etched using He LTP, and

80 ylideneglycerol penta(ethylene glycol) using methyl methacrylate followed by acetone deprotection via

81 eir application toward the polymerization of methyl methacrylate for the synthesis of polymers with p

82 nantly polyethylene, polypropylene, and poly(methyl methacrylate) fragments (up to 85%).

83 l complexes in solution or dispersed in poly(methyl methacrylate) gave blue-shifted emissive Pt(IV) c

84 r films which, relative to the standard poly(methyl methacrylate) glass formed on cooling at standard

85 struction included composite Marlex mesh and methyl-methacrylate, Gore-Tex, or primary closure in 57%

86 alyst mediates polymerization of MMA to poly(methyl methacrylate) (>65% syndiotactic, >70 000 g/mol m

87 al and Cl atom initiated photodegradation of methyl methacrylate has been investigated in a 1080 L qu

88 tible blends of poly(vinyl acetate) and poly(methyl methacrylate) have been used to produce a series

89 oped a simple, miniaturized paper/PMMA (poly(methyl methacrylate)) hybrid microfluidic microplate for

90 rugosa) catalyzed the transesterification of methyl methacrylate in 1-butyl-3-methylimidazolium hexaf

91 des were used free radical polymerization of methyl methacrylate in order to obtain branched multiblo

92 e of lipase-catalyzed transesterification of methyl methacrylate in these ionic liquids and several o

93 ylate, ethyl acrylate, n-butyl acrylate, and methyl methacrylate) in broad molecular weight ranges an

94 polyvinyl chloride, polypropylene, and poly(methyl methacrylate) in the edible portion of five diffe

95 erizations with ethylene + methylacrylate or methyl methacrylate incorporate up to 11% acrylate comon

96 Methyl methacrylate is effectively polymerized by 1, wit

97 k, the rate of structural relaxation of poly(methyl methacrylate) is reduced by a factor of 2 at a fr

98 hydrophobic bonded phase in the series, poly(methyl methacrylate), is found to resolve the intact con

99 thyl methacrylate, producing stable PFS-poly(methyl methacrylate) latex suspensions.

100 d, densely grafted outer polystyrene or poly(methyl methacrylate) layer.

101 adsorbed biomimetic initiator to polymerize methyl methacrylate macromonomers with oligo(ethylene gl

102 eir photochemical behavior within rigid poly(methyl methacrylate) matrices.

103 ce layers of polystyrene domains in the poly(methyl methacrylate) matrix can result in 3D representat

104 DTV(2+) in a poly(methyl methacrylate) matrix was fluorescent with a spect

105 ess of small polystyrene domains in the poly(methyl methacrylate) matrix with nanometer-scale resolut

106 nd long-lived triplet states in a rigid poly(methyl methacrylate) matrix.

107 cesses can be reproduced efficiently in poly(methyl methacrylate) matrixes.

108 membrane in a poly(glycidyl methacrylate-co-methyl methacrylate) micro electric field gradient focus

109 amount of grafted poly(acrylic acid) on poly(methyl methacrylate) micro- and nanoparticles was quanti

110 Methods for fabricating poly(methyl methacrylate) microchips using a novel two-stage

111 The poly(methyl methacrylate) micromachined device was fabricated

112 ethacrylic acid (MAA) copolymer or a control methyl methacrylate (MM) copolymer were determined by MS

113 , polymerization process for L-lactide (LA), methyl methacrylate (MMA) and dehydrosilylation of alcoh

114 representative acrylic monomers, the linear methyl methacrylate (MMA) and its cyclic analog, biomass

115 chain transfer (co)polymerisation (CCTP) of methyl methacrylate (MMA) and methacrylic acid (MAA) are

116 ymerization of polar vinyl monomers [such as methyl methacrylate (MMA) and N,N-dimethylacrylamide (DM

117 Polymerization of methyl methacrylate (MMA) and n-butyl methacrylate (BMA)

118 late) (PMMA) gels prepared by copolymerizing methyl methacrylate (MMA) and various amounts of ethylen

119 mpact of cross-linker purity and addition of methyl methacrylate (MMA) as a comonomer on CE performan

120 lar weight control, while polymerizations of methyl methacrylate (MMA) from the same nanoparticles ex

121 zations and copolymerizations of styrene and methyl methacrylate (MMA) mediated by a highly active si

122 The incorporated methyl methacrylate (MMA) monomer accelerates the radica

123 As SCNP system we employed methyl methacrylate (MMA) statistically copolymerized wi

124 ciency of PMMA, facilitating the recovery of methyl methacrylate (MMA) with high yield and purity at

125 etween 1,5,6-trimethylpyrazinium-3-olate and methyl methacrylate (MMA) yielding a lactone-lactam has

126 Subsequent grafting with methyl methacrylate (MMA) yields PE-graft-PMMA with narr

127 omonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and styrene (STY).

128 nthesis of dendritic macromolecules based on methyl methacrylate (MMA).

129 btained, which can achieve >95% reversion to methyl methacrylate (MMA).

130 and tunable copolymerization reactivity with methyl methacrylate (MMA).

131 eful in the photocatalyzed polymerization of methyl methacrylate (MMA).

132 I) insertion polymerization catalysts toward methyl methacrylate (MMA).

133 xythiophene):poly(styrenesulfonate) and poly(methyl methacrylate)-modified PCBM are utilized as the h

134 prolactone)-block-poly[oligo(ethylene glycol)methyl methacrylate mono-methyl ether] (NP-PCL-POEGMA).

135 (II) IIP was prepared by copolymerisation of methyl methacrylate (monomer) and ethylene glycol dimeth

136 controlled synthesis of polystyrene and poly(methyl methacrylate) (Mw/Mn < 1.2) can be implemented wi

137 ions with traditional vinyl monomers such as methyl methacrylate, N,N-dimethylaminoethyl methacrylate

138 n of a high-molar-mass (M(n) 135 kg mol(-1)) methyl methacrylate-n-butyl acrylate-methyl methacrylate

139 alues (up to 42%), while hydrogermylation of methyl methacrylate occurs with low selectivity (<3/1) f

140 styrene (PS), poly(ethylene oxide), and poly(methyl methacrylate) of different molar masses and in di

141 persion analysis of spectra of films of poly(methyl methacrylate) on calcium fluoride (CaF(2)) and si

142 and poly(dimethylaminoethyl methacrylate-co-methyl methacrylate) p(DMAEMA-co-MMA) were synthesized v

143 ) (pMMA), poly(3-sulfopropyl methacrylate-co-methyl methacrylate) p(SPMA-co-MMA), and poly(dimethylam

144 e) (PDMAEMA) and poly(n-butyl acrylate-block-methyl methacrylate) (PBA-b-PMMA).

145 c block co-polymer poly(ethylene oxide-block-methyl methacrylate)(PEO-b-PMMA) was used to fabricate r

146 Amphiphilic polyethylene oxide (PEO)-Au-poly(methyl methacrylate), PEO-Au-poly(tert-butyl acrylate) a

147 rylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA), was synthesized and eval

148 rylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA), which can be modified ea

149 the use of a layered composite of PMMA (poly-methyl-methacrylate), PHEMA (poly-hydroxyl-ethyl-methacr

150 7 K in an organic glass substrate and a poly(methyl methacrylate) plastic substrate.

151 hin polymer films of these compounds in poly(methyl methacrylate) (PMM) have been cast by solvent eva

152 Despite its proven cytotoxicity, poly-methyl methacrylate (PMMA) resin is one of the most freq

153 Poly-methyl methacrylate (PMMA)-based dental resins with stro

154 r materials calcium sulfate (CaSO4) and poly methyl methacrylate (PMMA).

155 geometry consisted of a 0.2-2.2-microm poly(methyl)methacrylate (PMMA) over-layer deposited on the s

156 Ultrathin poly(methyl methacrylate) PMMA films were prepared on gold su

157 used with a reference line coated with poly (methyl methacrylate) (PMMA) and a sensing line coated wi

158 ve velocity, various polymers including poly(methyl methacrylate) (PMMA) and cyanoethyl cellulose (cu

159 dye, IRD800, when it was deposited onto poly(methyl methacrylate) (PMMA) and measured in the dry stat

160 depositing toluene solutions containing poly(methyl methacrylate) (PMMA) and NAI-DMAC onto optical su

161 chieving up to 82 % depolymerization of poly(methyl methacrylate) (PMMA) and poly(alpha-methylstyrene

162 isomers (isotactic and syndiotactic) of poly(methyl methacrylate) (PMMA) are reported.

163 0 succinate (TPGS), Polysorbate 80, and poly(methyl methacrylate) (PMMA) as analytes.

164 d for the preparation of capsules using poly(methyl methacrylate) (PMMA) as the encapsulant and ethyl

165 at the selectivity and sensitivity of a poly(methyl methacrylate) (PMMA) based QCM sensor can be sign

166 olyethylene (PE), polystyrene (PS), and poly(methyl methacrylate) (PMMA) beads with diameters of 100-

167 ylic acid (PAA) block and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to simil

168 ng deuterated polystyrene (d(8)-PS) and poly(methyl methacrylate) (PMMA) blocks, as well as a short m

169 tion detection reaction (LDR) and (2) a poly(methyl methacrylate) (PMMA) chip for the detection of th

170 nent dipoles in commonly used spherical poly(methyl methacrylate) (PMMA) colloids, suspended in an ap

171 ization, "nacre-mimetic" hydroxyapatite/poly(methyl methacrylate) (PMMA) composites are developed by

172 nt approach for the depolymerization of poly(methyl methacrylate) (PMMA) copolymers synthesized via c

173 We describe a poly(methyl methacrylate) (PMMA) dip-coating procedure, which

174 stretching modes associated with a thin poly(methyl methacrylate) (PMMA) film that is coupled to a si

175 ching behaviors in toluene, chloroform, poly(methyl methacrylate) (PMMA) film, and powder state, whil

176 used to measure the damage of spin-cast poly(methyl methacrylate) (PMMA) films under 5-keV Cs(+) and

177 bricated without using the conventional poly(methyl methacrylate) (PMMA) for graphene transfer from a

178 Poly(methyl methacrylate) (PMMA) gels prepared by copolymeriz

179 the use of CO2 laser micromachining on poly(methyl methacrylate) (PMMA) has the potential for flexib

180 A recyclable poly(methyl methacrylate) (PMMA) is synthesized by incorporat

181 blue wavelengths (450-470 nm) both in a poly(methyl methacrylate) (PMMA) matrix and in solution at 77

182 film electrodes on the outer side of a poly(methyl methacrylate) (PMMA) microchip (without contactin

183 The poly(methyl methacrylate) (PMMA) microchips feature integral

184 capillary electrophoresis separation in poly(methyl methacrylate) (PMMA) microchips.

185 f study were surface chemistries within poly(methyl methacrylate) (PMMA) microfluidic channels that e

186 e serum albumin (BSA), respectively, on poly(methyl methacrylate) (PMMA) micropillar surfaces, as wel

187 to manipulate conductive silver-coated Poly(methyl methacrylate) (PMMA) microspheres (50 mum diamete

188 rate separation of polystyrene (PS) and poly(methyl methacrylate) (PMMA) microspheres based entirely

189 rsatile electrodes were templated into poly (methyl methacrylate) (PMMA) molds with a 3D printing pen

190 dehydrogenase (apo-GDH), is loaded into poly(methyl methacrylate) (PMMA) nanospheres in the presence

191 Poly(methyl methacrylate) (PMMA) optical fibers in a series o

192 The system utilizes a poly(methyl methacrylate) (PMMA) or glass substrates sputtere

193 ontaining polar monomeric units such as poly(methyl methacrylate) (PMMA) or polyethylene terephthalat

194 ce composed of thermoplastic material, poly (methyl methacrylate) (PMMA) performing a sophisticated a

195 device sealing, channels in an embossed poly(methyl methacrylate) (PMMA) piece are filled with a heat

196 sign involves manually rotating the top poly(methyl methacrylate) (PMMA) plate over the bottom plate

197 omposition, and is often blended with a poly(methyl methacrylate) (PMMA) polymer.

198 per-coated dielectrics, resonators with poly(methyl methacrylate) (PMMA) provided the best SNR/line s

199 As poly (methyl methacrylate) (PMMA) remains the main material em

200 nes can be stabilised by using a porous poly(methyl methacrylate) (PMMA) sacrificial layer, which cre

201 The cells were grown on electrospun poly(methyl methacrylate) (PMMA) scaffolds with a diameter of

202 eatly simplified method for fabricating poly(methyl methacrylate) (PMMA) separation microchips is int

203 clusters of electromagnetically coupled poly(methyl methacrylate) (PMMA) spheres with wavelength-scal

204 parated by smaller (approximately 3 mm) poly(methyl methacrylate) (PMMA) spherical beads, threaded on

205 t to separate these factors, we studied poly(methyl methacrylate) (PMMA) standards using two differen

206 stituted by a microchannel assembled in poly(methyl methacrylate) (PMMA) substrate connected to an am

207 moisobutyryl bromide was immobilized on poly(methyl methacrylate) (PMMA) substrates activated using a

208 rbon nanotubes are press-transferred on poly(methyl methacrylate) (PMMA) substrates and are easily co

209 The VG system exploited poly(methyl methacrylate) (PMMA) substrates of high optical q

210 A new method for thermally bonding poly(methyl methacrylate) (PMMA) substrates to form microflui

211 antibody bionanocomposite directly on a poly(methyl methacrylate) (PMMA) surface (also known as plexi

212 oms on pristine and electron-irradiated poly(methyl methacrylate) (PMMA) surfaces at 300 K has been s

213 eport here the chemical modification of poly(methyl methacrylate) (PMMA) surfaces by their reaction w

214 y prepared solid supports consisting of poly(methyl methacrylate) (PMMA) that provide enhanced perfor

215 o microfluidic channels hot-embossed in poly(methyl methacrylate) (PMMA) to allow the detection of lo

216 A poly(methyl methacrylate) (PMMA) topcoat further improves cyc

217 nanoparticles through the formation of poly(methyl methacrylate) (PMMA) triple-helices.

218 hange can be achieved through tuning of poly(methyl methacrylate) (PMMA) triple-helix stereocomplexes

219 by electrophoresis chips fabricated in poly(methyl methacrylate) (PMMA) using hot embossing techniqu

220 array was suitably interfaced with a poly- (methyl methacrylate) (PMMA) well-containing holders resu

221 elements (FVEs) in polystyrene (PS) and poly(methyl methacrylate) (PMMA) were investigated using the

222 Micrometer-sized glass tablets and poly(methyl methacrylate) (PMMA) were mixed and structured by

223 FF) has been used for the separation of poly(methyl methacrylate) (PMMA) with regard to molecular mic

224 ch as polyethylene terephthalate (PET), poly(methyl methacrylate) (PMMA), and polystyrene (PS), offer

225 depth profile spin-cast multilayers of poly(methyl methacrylate) (PMMA), poly(2-hydroxyethyl methacr

226 A series of copolymers poly(methyl methacrylate) (pMMA), poly(3-sulfopropyl methacry

227 Four different polymers, poly(methyl methacrylate) (PMMA), poly(ethylene terephthalate

228 face of the EGaIn nanodroplets(13) with poly(methyl methacrylate) (PMMA), poly(n-butyl acrylate) (PBM

229 Silanized glass, poly(methyl methacrylate) (PMMA), polycarbonate, and poly(dim

230 Easily accessible poly (methyl methacrylate) (PMMA), polyethylene terephthalate

231 Poly(methyl methacrylate) (PMMA), polystyrene (PS), and polyb

232 tion properties from the thermoplastics poly(methyl methacrylate) (PMMA), polystyrene (PS), polycarbo

233 val is used for the depolymerization of poly(methyl methacrylate) (pMMA), synthesized via reversible

234 ally combined with other polymers, like poly(methyl methacrylate) (PMMA), though the incorporation of

235 e of the nanocolumn, which consisted of poly(methyl methacrylate) (PMMA), was activated with an O(2)

236 eratures (Tg), polyetherimide (PEI) and poly(methyl methacrylate) (PMMA), were used to make the reusa

237 1-phenyl-1-H-benzimidazole) (TPBi), and poly(methyl methacrylate) (PMMA), without any exciplex format

238 hnique, we managed to baseline separate poly(methyl methacrylate) (PMMA)- and polystyrene (PS)-based

239 n principles, namely, laser-writing and poly(methyl methacrylate) (PMMA)-assisted lithographic proces

240 eam lithography at sites of interest on poly(methyl methacrylate) (PMMA)-covered monolayer MoS2 trian

241 zed toward photochemical ligand loss in poly(methyl methacrylate) (PMMA).

242 polymers such as polystyrene (PSR) and poly(methyl methacrylate) (PMMA).

243 of functional sample plates composed of poly(methyl methacrylate) (PMMA).

244 erties to petroleum-based linear analog poly(methyl methacrylate) (PMMA).

245 dely used polymers polystyrene (PS) and poly(methyl methacrylate) (PMMA).

246 ethylene (LLDPE), polystyrene (PS), and poly(methyl methacrylate) (PMMA).

247 materials such as polystyrene (PS) and poly(methyl methacrylate) (PMMA).

248 Herein, a photothermally responsive poly (methyl methacrylate) (PMMA)/paper hybrid disk (PT-Disk)

249 solvent-induced self-assembly of mixed poly(methyl methacrylate) (PMMA)/polystyrene (PS) brushes on

250 es of microfluidic channels poised on a poly(methyl methacrylate), PMMA, chip.

251 150 mum depth) that were replicated in poly(methyl methacrylate), PMMA, from a metal mold master.

252 ated planar waveguide was fabricated in poly(methyl methacrylate), PMMA, using a single-step, double-

253 For the first time, stereoregular poly(methyl methacrylates) (PMMAs) were separated according t

254 polymer systems, including polystyrene, poly(methyl methacrylate), poly-L-lactic acid, polycaprolacto

255 a phase separated poly(2-vinylpyridine)/poly(methyl methacrylate) polymer thin film.

256 Porphyrin-doped hybrid PMMA [poly(methyl methacrylate)] polymer films demonstrate the reve

257 apable of switching stereospecificity of the methyl methacrylate polymerization produces the highly s

258 , pH = 11.9), enabled the separation of poly(methyl methacrylate), polypropylene, and polyethylene NP

259 sants in the microemulsion polymerization of methyl methacrylate, producing stable PFS-poly(methyl me

260 s, kinetics of an ATRP reaction with a model methyl methacrylate propagating radical.

261 lues for functionalized graphene sheet- poly(methyl methacrylate) rivaling those for single-walled ca

262 or polystyrene-block-polyethylene-block-poly(methyl methacrylate) (SEM), well-defined worm-like CCMs

263 ents of different isomers of butanol on poly(methyl methacrylate) sheets, zinc oxide thick films, and

264 CN stretch of phenyl selenocyanate) in poly(methyl methacrylate) show that the probe dynamics are hi

265 Here, we design model poly(methyl methacrylate)-silica and poly(2-vinyl pyridine)-s

266 ferred to the polymer substrate by molding a methyl methacrylate solution in a sandwich (silicon mast

267 omatography (SEC) for the separation of poly(methyl methacrylate) standards with molar masses between

268 al protein in plastic materials such as poly(methyl methacrylate, styrene, vinyl acetate, and ethyl v

269 -embossed microchannels fabricated in a poly(methyl methacrylate) substrate.

270 lvent was a acetone/ethanol mixture for poly(methyl methacrylate) substrates or a dimethylformamide/a

271 These dyes were immobilized in a poly(methyl methacrylate) support, and the resulting dosimete

272 ur zip code probes immobilized onto the poly(methyl methacrylate) surface directed allele-specific li

273 nels reversibly sealed to photomodified poly(methyl methacrylate) surfaces to serve as stencils for p

274 three-dimensional (3D) printing pen and poly(methyl methacrylate) template.

275 05 wt% functionalized graphene sheet in poly(methyl methacrylate) there is an improvement of nearly 3

276 ol(-1)) methyl methacrylate-n-butyl acrylate-methyl methacrylate triblock copolymer with unprecedente

277 5 mum radius silica and 9.8 mum radius poly(methyl methacrylate) tubes and automated time/pressure b

278 Performance plastics, such as poly(methyl methacrylate), underpin the modern economy.

279 er consisting of styrene sulfonate units and methyl methacrylate units bearing poly(ethylene glycol)

280 ctured in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes on-chip valving, and is

281 enesulfonyloxy)anthracene-1,9-dicarboxyimide-methyl methacrylate (VBSADI-MMA) and N-(p-vinylbenzenesu

282 or cis-cyclooctene, indene, methyl acrylate, methyl methacrylate, vinyl methyl ketone, tert-butylethy

283 om transfer radical polymerization (ATRP) of methyl methacrylate was investigated using several pheno

284 Images of a CD phantom with polymerized methyl methacrylate were acquired with SF and full-field

285 ising different ratios of butyl acrylate and methyl methacrylate were prepared with similar degree of

286 ctionalized random copolymers of styrene and methyl methacrylate were spin coated or transferred, the

287 iphatic alkenes, and even electron-deficient methyl methacrylate were successfully functionalized.

288 lastic forms of anionic polystyrene and poly(methyl methacrylate), where their introduction disrupted

289 block-copolymers based on poly(styrene-block-methyl methacrylate) with various molecular weights and

290 erization of 2-hydroxyethyl methacrylate and methyl methacrylate yielded 100 nm thick films in 10 and