ライフサイエンスコーパス: particle size

1 hat is 6 orders of magnitude larger than the particle size.

2 whether microorganisms prefer to adhere to a particle size.

3 ld spikes and using minor proteins to define particle size.

4 glycol and drug formulation, on the aerosol particle size.

5 rface area, structural anisotropy, and small particle size.

6 lysis rate decreased with increasing mineral particle size.

7 avior of spinel ZnFe(2)O(4) as a function of particle size.

8 eased with the number of injections and with particle size.

9 icted, translating into an overestimation of particle size.

10 e than with PAC, likely due to the increased particle size.

11 ignificantly (p < 0.05) increased the powder particle size.

12 overage attaining values comparable with the particle size.

13 in new form factors, especially in terms of particle size.

14 ng and separation efficiency of the specific particle sizes.

15 devices only work well for a narrow range of particle sizes.

16 le size, being lower in samples with smaller particle sizes.

17 -RE nanoalloys with tunable compositions and particle sizes.

18 90% and did not strikingly alter the median particles size.

19 onsistent flow rates entering NTA for proper particle sizing.

20 s by monitoring the associated change in the particles' size.

21 ee trunk), food shape (cuboid or flattened), particle sizes (0.45-1, 1-2, 2-3, or 3-4 mm), and placem

22 ut remarkably also with the increase in mean particle size (1.5-5 nm).

23 lation of GEOs in water-based microemulsion (particle size 10.1nm) showed better antimicrobial activi

24 Embolization with combined particle sizes (100-500 mum) did not relate to symptom r

25 mum conditions were: steaming time 4.36 min, particle size 23 mm, time from harvesting to steaming 2

26 gamma-Al(2)O(3) with three particle sizes (5, 35, and 70 nm) was used as an analogu

27 red the zeta potential (-47.5 to -40.8), and particle size (74.23 to 55.35 nm).

28 (diameter 18-26 nm) (-0.02 SD LDL defined by particle size; 95% CI: -0.10 to 0.05 for CETP versus -0.

29 etallic NPs (Pt(3) M/rGO-HF) with ultrasmall particle size (about 3 nm) and dramatic monodispersity.

30 The two particle sizes affected the water-holding capacity (WHC)

31 (3) M intermetallic NPs exhibit the smallest particle size among the reported ordered Pt-based interm

32 The particle size analysis and confocal micrographs of diges

33 Particle size analysis indicated that the microcapsules

34 aph, X-ray photoelectron spectroscopy (XPS), particle size analysis, and fluorescence spectrum (FL) a

35 s have an identical Pt loading, similar Beta particle size and acidity, but different internal struct

36 The influence of particle size and chemical composition of three differen

37 ceeds a critical value, which depends on the particle size and chemical composition.

38 used to infer important properties, such as particle size and concentration.

39 on of supported metal catalysts with uniform particle size and coordination environment is a challeng

40 cal power absorption and is also affected by particle size and corresponding particle suspension heig

41 Increasing particle size and decreasing negative surface charge wer

42 we speculate on the observed differences in particle size and density that we found between young pa

43 Engineering the particle size and Fe doping is critical to control extri

44 particulate organic carbon, depending on the particle size and filtration method, and overlook its re

45 in consumer products, there is evidence that particle size and formulation influences skin permeabili

46 starch, associated with their higher average particle size and greater amylose content.

47 Low-density lipoprotein particle size and high-density lipoprotein, small and me

48 Downscaling the particle size and increasing the operating pressure led

49 ryo-SEM results further showed a decrease in particle size and loss of internal "polyhedral" structur

50 accordance to its higher surface area, lower particle size and lower charge transfer resistance.

51 Here, by independently controlling particle size and particle loading using colloidal nanoc

52 pability was found through the match between particle size and pillar spacing, being consistent with

53 Crosslinking increased the particle size and poly-dispersity, and led to the format

54 ysisorption yields quantitative agreement in particle size and qualitative agreement in average speci

55 poral mapping of the pH, dry matter content, particle size and rheological properties.

56 roscope (DHM) enabling determination of both particle size and RI of individual subwavelength particl

57 The albedo, texture, particle size and roughness are beyond the spacecraft de

58 We describe the effect of varying particle size and shape on the SERS signal, focusing on

59 The correlation between the particle size and structural properties of the PS MPNPs

60 conventional vapor-phase deposition, and the particle size and structural uniformity enable comparati

61 In particular, the influence of particle size and surface chemistry are discussed, in or

62 operties (such as pore size, total porosity, particle size and surface distribution of peptide on the

63 ly involves a tedious sequence that controls particle size and surface properties in separate steps.

64 cohesive gel resulted in the highest median particle size and the most viscoelastic chyme.

65 By measuring the particle size and the particle number distribution, we w

66 The effect of flocculant concentration on particle size and viscosity of SBW was also evaluated.

67 ions, the device can be adapted to different particle sizes and flow rate ratios.

68 ides having different crystal structures and particle sizes and measured the power densities they pro

69 icle, but instead requires a distribution of particle sizes and/or properties.

70 pure, homogeneous nanomaterial preparations, particle sizing and counting remains difficult for heter

71 ingle sEVs, not discernable via conventional particle sizing and counts alone.

72 to the understanding and rational control of particles size and size distributions.

73 th a 3% cross-linking density, a 200-300 mum particle size, and 100 g external load.

74 erial parameters include filler type, filler particle size, and filler-binder bonding.

75 es relationships among the refractive index, particle size, and pattern both numerically and experime

76 Zeta potential, particle size, and polydispersity index of Betalain NLs

77 The spatial distribution, concentration, particle size, and polymer compositions of microplastics

78 The cross-linking density, external load, particle size, and repeatability of energy recoverabilit

79 The combined influence of LM concentration, particle size, and sedimentation is explored.

80 found that the applied current, the CaCO(3) particle size, and the feed rate affect the removal of p

81 The tribofilm composition, particle size, and type of contact are identified as imp

82 erview of the state of the art morphologies, particle sizes, and optical properties of YAG:Ce on the

83 Chemical compositions, particle sizes, and thermal properties of the studied fl

84 As smaller particle sizes are increasingly included in microplastic

85 he most effective factors for tuning droplet/particle sizes are PLGA concentrations and the flow rate

86 lms: more than 1100 particles mum(-2) with a particle size as small as ~5 nm can be achieved via stra

87 cle counting and EBC was calculated for each particle size as well as the cut-off points that optimiz

88 to different Co(3)O(4) catalyst loadings and particle sizes as well as the mixed Ag + Co(3)O(4) catal

89 NPs) system capable of exhibiting different particle size at different temperature was developed, wh

90 related to the lipid type but rather to the particle size, being lower in samples with smaller parti

91 rmulated microparticles had a mean geometric particle size between 2 and 5 mum, entrapment efficiency

92 ntical physical characteristics to determine particle size but differ in the weighting of the distrib

93 of micellization and subsequent evolution in particle size can be studied when preparing PGMA(29)-PMO

94 varied according to bean genotype and powder particle size: coarse powders resulted in larger (+26%)

95 UPLC(R) BEH C18 (50 mm x 2.1 mm i.d., 1.7 mm particle size) column was employed.

96 Optimisation of the stationary phase nature, particle size, column length and internal diameter, as w

97 P = 0.0008, respectively) and increased LDL particle size compared with the milk diet (P = 0.02).

98 pulation, porosity increases with increasing particle size, consistent with the proposed UMN growth m

99 Mn-O stretching Raman bands also varied with particle size, consistent with the ratio of edge to bulk

100 ) concentration, relative humidity (RH), and particle size control reaction rates and mechanisms.

101 ermeability of 143 L m(-2)h(-1)bar(-1) and a particle size cut off of 35 nm.

102 H) to increase membrane selectivity, and the particle size cutoff was reduced from 35 to 10 nm post-t

103 Mean particle size decreased as pressure and pass number incr

104 As particle size decreased, polymer degradation increased,

105 displayed higher scattering intensities in a particle-size dependent manner.

106 f the epithelial lining fluid by considering particle-size-dependent respiratory deposition.

107 r viruses using single-particle tracking and particle-size determination.

108 perimental results revealed that the average particle size diameter of Horse chestnut starch nanopart

109 cholesterol concentrations in LDL defined by particle size (diameter 18-26 nm) (-0.02 SD LDL defined

110 NP had an average diameter of 210 nm, narrow particle size distribution (polydispersity index ~0.1),

111 The particle size distribution (PSD) and the stability of na

112 A particle size distribution (PSD) estimation method based

113 Field measurements of the time-resolved particle size distribution (PSD) in a typical room envir

114 The input parameters of the model are particle size distribution (PSD), bulk density, and resi

115 Varying surface particle size distribution (via the slope of the particl

116 The steady-state current scales with the particle size distribution and is limited by the diffusi

117 ules were also additionally analyzed for the particle size distribution and morphological characteriz

118 Particle size distribution and morphology of the PSO pow

119 pproach of incremental complexity to measure particle size distribution and size stability of NEPs, c

120 s into both the average mass of a structured particle size distribution and the average hydrodynamic

121 uences of the soiling of PV modules from the particle size distribution and the cleanliness value.

122 /mL) presented the best properties regarding particle size distribution and zeta potential.

123 cle tracking analysis, with the variation in particle size distribution being used to determine the r

124 PEVs were assessed by total count and particle size distribution by Nanoparticle Tracking Anal

125 Understanding the particle size distribution in the air and patterns of en

126 We measured particle size distribution of wheat flour, photographed

127 d not differ in terms of dry matter content, particle size distribution or rheological properties.

128 EP assessment, including the measurements of particle size distribution, and are offering wide access

129 o simultaneously determine EV concentration, particle size distribution, and surface immunophenotype.

130 ization function, relative particle density, particle size distribution, and water column density str

131 dictated by an interplay between the aerosol particle size distribution, composition, water availabil

132 Neither particle size distribution, nor cell destruction, nor pl

133 Particle size distribution, of around 40 and 100 nm for

134 Starch damage, morphology, particle size distribution, pasting, thermal property, a

135 the formulations in terms of particle size, particle size distribution, product yield, entrapment ef

136 ticle sizer to measure the time evolution of particle size distribution, which was used to calculate

137 mplexes were studied by measuring turbidity, particle size distribution, zeta-potential, as well as s

138 tment (roasted) and ground to a standardised particle size distribution.

139 astructure of the flour and fiber by SEM and particle size distribution.

140 ions, which were probed via the evolution of particle size distribution.

141 ws unbiased fitting of the information-laden particle-size distribution (PSD) including its shape.

142 dy modelled the effects of discretization of particles size distribution on sediment deposition and p

143 , the effect of rapid cooling on the silicon particle size, distribution, and morphology of hypereute

144 ing microencapsulation was characterized by: particle size/distribution (span), morphology, drug/gela

145 -gas concentration ratios also depend on the particle size distributions and aerosol loadings in the

146 ch sediments, which differ slightly in their particle size distributions and morphologies but exhibit

147 AFM and dSTORM particle size distributions showed coherent unimodal and

148 locity technique that allows us to determine particle size distributions while accounting for colloid

149 te not only important 1D distributions, i.e. particle size distributions, but also nanoparticle struc

150 ual roast intensity and ground to comparable particle size distributions.

151 on of pH, surface area (SA) and ferrihydrite particles size distributions.

152 n were characterized in terms of morphology, particle size, drug encapsulation efficiency, in vitro r

153 Sulfate shifts to larger particle sizes during the event, indicative of fog/cloud

154 f natural aluminum oxides to investigate the particle size effect.

155 spectra (mu(s)') were found less useful for particle size estimation as they lack a characteristic s

156 nutraceutical whereas flours with a smaller particle size (F3 and F4) are more interesting as functi

157 tion, neutralization kept a stable colloidal particle size for pHs decreased to pH 9,8 and 7; however

158 rce-to-receiver distance, printer positions, particle size fraction, and environmental diffusivity es

159 l, and cobalt) were synthesized with average particle sizes from 0.9 to 1.4 nanometers, with tight si

160 ide range of orders of magnitude for a given particle size group.

161 ons (62-84% of total P) by NMR regardless of particle size (>=10 or 1-10 mum).

162 cording to this, microplastics in detectable particle sizes (>100 mum) are only found on the surface

163 The cornmeal with smaller particle size had higher RS content (202 mg/g).

164 ring microfluidisation resulted in a smaller particle size, higher WRC and extractability, and an inc

165 d high-density lipoprotein, small and medium particle size (HMSP), GlycA, LP-IR, short-chain dicarbox

166 , a greater porosity, lower agglomerates and particle size, improve the Ca solubility in the intestin

167 Analysis of particle size in each recovered fraction served to asses

168 1, the Just Noticeable Difference (JND) for particle size in melted chocolate was ~5 mum in a partic

169 egrees C, protein surface hydrophobicity and particle size increased and alpha helical structure decr

170 stributions along a continuum of behavior as particle size increases and slopes get steeper and/or sm

171 Aerosol particle size influences aerosol Fe fractional solubilit

172 nates the early stages of discharge when the particle size is about 6-9 nm.

173 When the particle size is around 1 mum or below, studies on SAW m

174 e observed effect to be general and that the particle size is the single most important factor govern

175 to control samples, heat treatment increased particle size, light absorbance, centrifugal instability

176 This particle size limit is only an order of magnitude larger

177 ula: see text] describes the degree to which particle size lowers the melting point and is found to v

178 Two bean powder particle sizes (<=0.5 mm, <=1.0 mm) were investigated.

179 Under optimized conditions (particle size, <0.5 mm; feed rate, 0.4 L/d; current, 5 m

180 We used a particle size magnifier and a scanning mobility particle

181 We show that IM-MS yields a 2D particle size-mass distribution function, which in turn

182 The particle size measurements, functional properties and an

183 regation, as evidenced by surface charge and particle size measurements.

184 The mucin particle size method was employed to characterize mucin-

185 size) on important properties of wheat bran (particle size, microstructure, chemical composition, wat

186 on microscopy that enables the corresponding particle size, morphology, crystallinity, and other fact

187 The key parameters essential for tailoring particle size, morphology, porosity, acid-base, and redo

188 cles with identical compositions but varying particle size, morphology, stabilizer chain length, and

189 ormulation was characterized with respect to particle size, morphology, surface charge and singlet ox

190 in genogroups, with small, medium, and large particle sizes observed.

191 The average particle size obtained was 59.3 (2.60) nm-161.0 (27.30)

192 ferent composites was 10 to 224 uM for a BAG particle size of <5 to 150 um in the presence of artific

193 ger nut milk were spherical with and average particle size of 1.01 mum.

194 d along an axis 76 angstrom long and maximal particle size of 120 angstrom.

195 ticles by solvent evaporation, with the mean particle size of 122.0 +/- 2.28 nm and drug loading of 3

196 by solvent evaporation, resulting in a mean particle size of 125.6 +/- 2.3 nm and drug loading of 10

197 rate of 900 rpm yielding the lowest average particle size of 130 nm.

198 Tungsten disulfide (WS(2)) with an average particle size of 2 mum was found to increase the sensiti

199 MSs were spherical, with a mean particle size of 29.04 +/- 1.89 mum rendering them suita

200 -TEM revealed an average core metallocorrole particle size of 32 nm, with protein tendrils extending

201 d that the microcapsules obtained had a mean particle size of 60.97 um.

202 ated nanoparticles (ApoE-NPs), with the mean particle size of 64 nm and drug loading of 10% (w/w).

203 at a N:P ratio of 6 demonstrated an average particle size of 76.6nm with a zeta potential of +16.5mV

204 (PLGA) microspheres (Sunb-malate MS) with a particle size of approximately 15 mum and a drug loading

205 Ejecta with a size much larger than the mean particle size of feedstock powder have been observed in

206 The effect of fat content and particle size of ground mustard seeds on formation and r

207 Average particle size of HSC, WSC and LSC based nano-particles w

208 Overall a lower particle size of JF resulted in a close structure of bre

209 cles without any loss in reaction yields and particle size of nanoparticles.

210 The mean particle size of surface-decorated nanoliposomes (SDNLs)

211 Moreover, the particle size of the aggregated molecules gradually incr

212 om the moderately alkaline pH and very small particle size of the burial soil, in addition to bronze

213 The average particle size of the curcumin nanoparticles was 66 nm.

214 According to the particle size of the JF, the amount of water added to do

215 r and gas interaction and the mineralogy and particle size of the slag are the main factors that have

216 The particle size of US nanoliposomes ranged between 40 and

217 ions, 5FU-SLN(4) was the most effective with particle size of was 263 +/- 3 nm, zeta potential was 0.

218 and maize starch (QR and MR) showed average particle sizes of 107 and 222 nm, encapsulation efficien

219 pants, two solid commercial chocolates (with particle sizes of 19 and 26 mum; i.e., just above the JN

220 Scanning electron microscopy demonstrated particle sizes of 3-100 mum.

221 ructural elements of FeN(4) sites, including particle sizes of catalysts, Fe content, and Fe-N bond s

222 dified, at least in part, suggesting reduced particle sizes of dietary chitin in the stomach.

223 We report masses and hydrodynamic particle sizes of insoluble particles formed from the da

224 of this work was to determine the effect of particle sizes of Prosopis flour on its chemical composi

225 oyed to encapsulate the chlorophyll, and the particles size of the composites was controlled through

226 However, the effects of particle size on bactericidal activity and fruit element

227 The effect of particle size on hemicellulose recovery upon pretreatmen

228 , will allow new insights into the effect of particle size on performance.

229 resence of water increase monotonically with particle size on Pt-rich catalysts, suggesting that the

230 red plastic debris and the impact of plastic particle size on removal remain largely unexplored.

231 nce of viscosity to predict the influence of particle size on the glass transition temperature and vi

232 sults highlight the fundamental influence of particle size on the uptake and release kinetics.

233 ticles with different shapes, densities, and particle sizes on different sediment beds were experimen

234 er of passes, bran concentration and initial particle size) on important properties of wheat bran (pa

235 d five times without any appreciable loss in particle size or catalytic activity.

236 omes without altering their surface markers, particle size or distribution.

237 interaction between particles by increasing particle size or external field strength leads to a pref

238 this interaction becomes stronger at reduced particle size or, equivalently, with increased surface t

239 l properties of the formulations in terms of particle size, particle size distribution, product yield

240 iculate complexants, and their dependence on particle size, particle type (i.e., reactive sites distr

241 The samples were characterized for the particle size, polydispersity index, zeta potential, app

242 butions showed coherent unimodal and bimodal particle size populations isolated via centrifugation an

243 critical physicochemical properties (such as particle size, porosity, average pore diameter, and drug

244 ) models that are capable of predicting PLGA particle sizes produced by different microfluidic system

245 model eventually allowed rapid prediction of particle sizes produced using various microfluidic syste

246 ion (~10 um) for samples with larger initial particle sizes proved crucial in improving signal stabil

247 cle size in melted chocolate was ~5 mum in a particle size range commonly found in commercial chocola

248 e fresh ship engine exhaust are in ultrafine particle size range.

249 hase fcc and has a powdery morphology with a particle-size range of 15-80 nm.

250 In total, 96% of the measurable particle sizes ranged from 10 to 36 nm.

251 as achieved by a jet mill and flours (JF) of particle size, ranged from 17 to 84 mum, were used.

252 a of polystyrene suspensions, with a nominal particle size ranging from 0.1 to 12 mum in diameter.

253 The NLCs presented particle sizes ranging from 148.23 to 342.10 nm, PDI fro

254 s of different alloy phases depending on PAE particle size ratio, DNA surface coverage, stoichiometri

255 ride and K(4)C(60) are selected according to particle size ratios.

256 Sample homogenisation and particle size reduction (~10 um) for samples with larger

257 Interestingly, particle size reduction from homogenization drastically

258 Additionally, particle size-resolved results are readily obtained.

259 t high space velocity in the literature, the particle-size-resolved fresh filtration efficiency of se

260 urfaces have identified features such as the particle size, shape and surface charge to influence the

261 elleted base diet, we test for the effect of particle size, shape, and amount on DMT.

262 ential information to proper risk assessment-particle size, shape, and chemical composition have to b

263 les can change significantly with changes in particle size, shape, composition, and arrangement.

264 and reliable method for the determination of particle sizes, shapes, and numbers is missing, as exist

265 It was observed that particle size significantly influences hemicellulose rec

266 red by US and MF were characterized based on particle size, structure and stability.

267 factants were present in the entire range of particle sizes, supporting recent works.

268 color degradation was better associated with particle size than conjugation and was lowest for PPI-st

269 reated casein aggregates of larger colloidal particle size than primary casein micelle in control MPI

270 Despite similar Pt metal particle size, the AT catalyst is significantly more act

271 C-G material was compared to GAC of the same particle size, the clay-matrix, and PAC.

272 The effect of wood particle size thereby particle specific surface area on

273 microfluidisation reduced wheat bran median particle size to 14.8 mum and disintegrated starch granu

274 Further increase the Ni particle size to 37.2 nm allows the H(2) evolution react

275 ass transport in the electric field, enables particle size to be estimated and explains the feasibili

276 It has been shown that reducing their particle size to nanoscale dimensions benefits overall e

277 carded oyster shells were ground to <=100 um particle size to produce oyster shell powder (OS).

278 n shifts are derived for the entire range of particle size under the rigid contact regime.

279 re, this linear dependency is insensitive to particle size variation within 20-200 nm range.

280 e-shell yields exceeding 99%, tuning the MOF particle size via the solution concentration of AuNRs.

281 from 5.139 mum to 8.453 mum as their median particle size visualized at x50.

282 ctive counterparts for the SQDs with similar particle sizes (volumes).

283 Particle size was also measured for each sample.

284 Particle size was controlled by the concentration of the

285 Majority particle size was found to be below 25 microns generally

286 The influence of particle size was investigated in the analysis of the su

287 nanoparticle tracking analysis and a larger particle size was observed for the oxidized treatment.

288 While the initial particle size was of minor importance, a higher pressure

289 In addition, the distribution of particles sizes was found to follow the IEST-STD-CC 1246

290 Increasing DS increased the particle size, water solubility, and swelling power, whi

291 Both alpha-Al dendrites and the silicon particle sizes were significantly reduced from micron to

292 eved a controlled aggregation with different particle size, which gives a series of different antibac

293 erical geometry progressively increased with particle size, which is consistent with the interpretati

294 -bound carbonyls) and aggregation (increased particle size); while subsequent wet heating induced par

295 sed gas velocity, particle concentration and particle size will exacerbate the erosion and wear rate

296 ictive particle trapping for three different particle sizes (with an estimation error < 10%, not usin

297 colates; as expected, the JND increased with particle size, with a Weber Fraction of ~0.17.

298 ed as a synthetic handle to directly control particle size, with potential implications for industria

299 ysicochemical properties such as morphology, particle size, zeta potential, pGFP encapsulation effici

300 The particle sizes, zeta potentials and encapsulation effici