ライフサイエンスコーパス: alkali

1 The upper phase, which contains an organic alkali 1-(2-hydroxyethyl) piperazine (HEP), is used for

2 , and stability (ESI) indexes) properties of alkali-(A-FPC), enzymatic-(E-FPC), and enzymatic-solvent

3 and durability toward hydrogen evolution in alkali, achieving current densities of 10 and 20 mA cm(-

4 ses for the isolation of beta-glucans, using alkali, acid or a combination of both, result in degrada

5 and alkaline pH, TMC-1 is only required for alkali-activated current, revealing a specificity for al

6 g through the decoration of graphene with an alkali adatom superlattice.

7 erse and stabilize precious metal atoms with alkali additives for the WGS and potentially other fuel-

8 The alkali-adducted 18-crown-6 ether ions, including (M + Li

9 alkali chloride mixture was introduced, all alkali-adducted analyte ions were simultaneously detecte

10 ective recognition of Ag(+) among 20 various alkali, alkaline earth and transition metal ions.

11 fully discriminate the 57 species, including alkali, alkaline earth, post-transition, transition, and

12 uated for 23 elements from the categories of alkali, alkaline earth, transition, and poor metals.

13 roup 9 transition metals Co, Rh, and Ir, the alkali, alkaline-earth, and rare-earth elements, and Sb4

14 e compared to what has been demonstrated for alkali and alkali earth metal ions.

15 rovides a basis for analyzing the binding of alkali and alkaline earth metal atoms over a broad range

16 Alkali and alkaline earth metal compounds in the dust di

17 The effect of alkali and alkaline earth metal ions on the reactions of

18 for this organ and others is that fluxes of alkali and alkaline earth metals are required for signal

19 e find a quite general phenomenon: among the alkali and alkaline earth metals, Na and Mg generally ha

20 experimentally shown that in the presence of alkali and alkaline earth salts, oxidation of Cr(III) ta

21 mics simulations to compare the solvation of alkali and alkaline-earth metal cations in water and liq

22 e compounds as optical molecular sensors for alkali and alkaline-earth metal cations.

23 compounds was facilitated through the use of alkali and alkaline-earth metals, which selectively fill

24 Further dilute alkali and dilute acid solubilised the remaining 10-40%,

25 ples exhibiting high delta(66)Zn, along with alkali and magnesian suite samples.

26 uses and nonatmospheric releases from chlor-alkali and mining result in an additional 540 Gg of Hg r

27 arides were much more readily extractable in alkali and molecular profiling revealed the presence of

28 ees C and 100 degrees C) and chemical (acid, alkali and reducing sugar) treatments on the IgY binding

29 tly enriched in xylan fractions extracted by alkali and subcritical water, which indicates their pref

30 Curcumin degraded in emulsion under acid, alkali and UV light.

31 es, independent factors associated with all, alkali, and acid injuries, and total ED-associated charg

32 es that are usually composed of strong acid, alkali, and bromine methanol, and are detrimental to the

33 Metal amidoborane compounds of the alkali- and alkaline earth metals have in recent years f

34 bidopsis lignins doubled their solubility in alkali at room temperature.

35 However, spontaneous emission in alkali-atom spin-orbit-coupled systems is hindered by he

36 n at P < 300 GPa was overcome by introducing alkali atoms as reductants.

37 s, light-induced atomic desorption (LIAD) of alkali atoms from the inner surface of a vacuum chamber

38 heory level, we found that the deposition of alkali atoms onto the molecular film leads to unusual re

39 diatomic molecules assembled from pre-cooled alkali atoms, but for the wider range of species amenabl

40 xperiments for the purpose of modulating the alkali background vapour.

41 al bicarbonate levels who might benefit from alkali before acidosis develops.

42 serum total CO2 and might benefit from oral alkali before overt acidosis develops.

43 s associated with an inability to produce an alkali bile during NESLiP.

44 are prepared by physical phase separation of alkali borosilicate glasses of suitable composition in c

45 monoliths, including sintering and fusion of alkali borosilicate initial glasses as well as partial o

46 nological components of retinal injury after alkali burn and explored a novel neuroprotective regimen

47 By stimulating corneal angiogenesis with an alkali burn in Tie2-GFP fluorescent-reporter mice, we ev

48 decreased corneal opacity in murine corneal alkali burn model by modulating inflammatory cytokines.

49 these processes was studied using the ocular alkali burn model system.

50 splanted into the mouse stroma 24 h after an alkali burn suppress the severe inflammatory response an

51 ventually enhanced corneal recovery from the alkali burn.

52 e findings illuminate the mechanism by which alkali burns cause retinal damage and may have importanc

53 Recurrent PUK with scleritis following alkali burns occurred in 5 male patients/6 eyes (median

54 Alkali burns to the eye constitute a leading cause of wo

55 e elevation was not observed in experimental alkali burns.

56 volves soluble toxic precursors, and acid or alkali catalysts, and requires multiple synthesis steps,

57 s positively correlates with the size of the alkali cation: NS/Cs(+)/NS > NS/Rb(+)/NS > NS/K(+)/NS >

58 It was observed that addition of alkali cations (K(+), Rb(+), and Cs(+)) led to the aggre

59 The co-adsorbed alkali cations along the step weaken the OH adsorption a

60 annels, do not discriminate among monovalent alkali cations and are permeable also to several organic

61 geometric and chemical compatibility of the alkali cations and the available phases, the interaction

62 vations on the identity and concentration of alkali cations on the non-Nernstian pH shift, and demons

63 Among the tested alkali cations, K(+) is the most efficient one to elevat

64 n metals (for example, Cd, Zn) as opposed to alkali cations, with tetrahedral coordination preference

65 s regenerated by O2, dissolving first in the alkali chloride melt, and in the second step dissociatin

66 When an alkali chloride mixture was introduced, all alkali-adduc

67 inless steel needle deposited with saturated alkali chloride solution was introduced into the mini ox

68 he FAPCI mass spectra when the corresponding alkali chloride solutions were separately introduced to

69 o 95% on catalysts comprising a mixed molten alkali chloride supported on a mildly redox-active Dy2O3

70 from ion counting (IC) experiments for mixed alkali chlorides and dsDNA.

71 is trend agreed with the lattice energies of alkali chlorides.

72 on, or by infiltration of fluids enriched in alkali components extracted from the subducted crust.

73 we can explain how, in both single and mixed alkali compositions, metal ion clustering and percolatio

74 The effects of glycerol concentration, alkali concentration, ultrasonication and treatment time

75 u(In, Ga)Se2 solar cell shows the matrix and alkali concentrations are wide-ranging.

76 the strong chemical resistance under extreme alkali conditions, these catalysts can be recycled witho

77 The alkali control strategy can also turn on an intermolecul

78 This paper explores the strategy of "alkali control," where the presence of an alkali metal c

79 beta-Chitin was more susceptible to alkali deacetylation than was alpha-chitin, and required

80 The alkali-doped fullerides show a transition from a Mott in

81 Samples were alkali dry-ashed, dissolved in water, and iodine assayed

82 In particular, AEFe2As2 (AE: Alkali earth elements, AE-122) is one of the best candid

83 to what has been demonstrated for alkali and alkali earth metal ions.

84 several alkali metals (Li, K, Rb and Cs) and alkali-earth Ca.

85 te ordered structure in which lanthanide and alkali-earth ions occupy alternate (001) layers and oxyg

86 n a case study on a new technology for chlor-alkali electrolysis to be introduced in Germany.

87 on and hydrogen evolution reactions in water-alkali electrolyzers is pivotal for large-scale and sust

88 ile elements (such as lead, zinc, indium and alkali elements) relative to CI chondrites, the meteorit

89 s attributable to a high pressure and strong alkali environment in the synthesis atmosphere; in this

90 nerally extracted by treatments with acid or alkali, enzyme, and microorganisms.

91 bdate species, nickel(II) diamine complexes, alkali-exchanged stannosilicate molecular sieves, and am

92 a-d-xylan was found as the majority (70%) of alkali extract and 4.2% of the dry matter acai pulp.

93 nd ACE-inhibitory activities) generated from alkali extracted HPI in the shortest time (2 h) compared

94 nvestigate effects of acetate and oxalate on alkali feldspar-brine interactions in a simulated geolog

95 Mono Lake's alkali flies are a compelling example of how the evoluti

96 Compared with six other species of flies, alkali flies are better able to resist wetting in a 0.5

97 hough superbly adapted to resisting wetting, alkali flies are vulnerable to getting stuck in natural

98 The remarkable alkali fly, Ephydra hians, deliberately crawls into the

99 fully transparent devices are fabricated on alkali-free glass and flexible polyimide foil, exhibitin

100 The alkali fullerides, A(3)C(60) (A = alkali metal) are mole

101 to study quantum effects in ultracold atomic alkali gases confined to non-trivial geometries.

102 Alkali generation by oral microbes, specifically via arg

103 vacuum gap breaks inversion symmetry in the alkali halide layer, inducing out-of-plane dipoles that

104 gradients induce concentration gradients in alkali halide solutions, and the salt migrates towards h

105 l and grain boundary-free film is grown with alkali halides as substrates.

106 It is shown the metal alkali halides could be used as universal substrates for

107 Alkali halides MX, have been viewed as typical ionic com

108 xplore the interface between ionic rock salt alkali halides such as NaCl or KBr and polar insulating

109 Squid pens were subjected to alkali hydrolysis to extract chitin and chitosan.

110 by treating the wings with the corresponding alkali hydroxide before spotting of analyte.

111 nated with elemental liquid Hg (mainly chlor-alkali industry) or phenyl-Hg (paper industry).

112 Alkali injuries were more common than acid injuries (53.

113 Alkali injury from bursting of chuna packets was the mos

114 An alkali injury was produced with a filter paper of 3 mm w

115 ion of TMC-1 confers alkaline sensitivity to alkali-insensitive cells.

116 io modeling of MnO2 to examine the effect of alkali-insertion, protonation, and hydration to derive t

117 eta-glucans are cross-linked, forming a huge alkali-insoluble complex with chitin and chitosan polyme

118 . restricta cell wall are almost exclusively alkali-insoluble, showing that they play an essential ro

119 , age, body mass index, and dietary acid and alkali intake, p.E161K SNP carriers had a nonsignificant

120 nism by which organic vapor exposure reduces alkali ion adduction in the positive mode involves the d

121 the other hand, has essentially no effect on alkali ion adduction.

122 shown to improve with increasing size of the alkali ion, reaching optimum conditions for the largest

123 or metal-centered reduction depending on the alkali ion.

124 e nanomaterials are promising electrodes for alkali-ion batteries owing to their distinct reaction me

125 able hole sizes that enable greatly enhanced alkali-ion storage properties.

126 We report that the addition of alkali ions (sodium or potassium) to gold on KLTL-zeolit

127 in creating -O linkages with more than eight alkali ions and establishing an active site on various s

128 i) superstructures that are characterized by alkali ions as well as Fe(II)/Fe(III) charge orderings i

129 rodes (Hg/Pt UMEs) were tested as probes for alkali ions in propylene carbonate (PC) in an oxygen- an

130 Besides alkali ions, other transition metal ions such as Ni(+),

131 into the mini oxyacetylene flame to generate alkali ions, which were reacted with analytes (M) genera

132 llent transport properties compared to other alkali ions.

133 The preferential release of alkalis is followed by an in situ repolymerization of th

134 solutions, covering a wide pH range (acid to alkali), is described.

135 n 1 and 2 orders of magnitude lower than the alkalis (K and Na).

136 ually estimated using an indirect technique, alkali labile phosphate (ALP), that assumes that vitello

137 D24-)) and DNA lesions (single strand breaks/alkali labile sites) were significantly increased in blo

138 um DinB1 extend the DNAppG primer to form an alkali-labile DNApp(rG)pDNA product.

139 as detected mostly in oligomeric form in the alkali-labile fraction and was enriched in tension wood.

140 ults in direct strand scission by generating alkali-labile fragments from the oxidized nucleotide.

141 Independent generation of this alkali-labile lesion at defined positions within nucleos

142 ase radical produces direct strand breaks or alkali-labile lesions in single or double stranded DNA.

143 With the cesium-based diode-pumped alkali laser and remote plasma etching of Si3N4 as examp

144 These findings suggest that the formation of alkali-leachable lignin domains rich in free phenolic gr

145 olution-deposited films have more oxygen and alkalis, less carbon and hydrogen, and smaller optical b

146 In the biochemical route 1, alkali lignin was chemically depolymerized into vanillin

147 Analysis of alkali-loaded mice revealed a significantly reduced abil

148 acellular pH (pHi ) recovery (decrease) from alkali loads in neurons and, surprisingly, adjacent astr

149 Natural green table olives (non-treated with alkali) make this product less attractive to consumers t

150 three groups, independent of the associated alkali metal (K or Na).

151 methyl ketones, malononitrile, bromine, and alkali metal acetates is reported.

152 r [M + K](+) ions of the FFAs, whereas other alkali metal adducts can be generated by treating the wi

153 ions reduce to Cu(I), Ni(I), and Fe(I) upon alkali metal adsorption, whereas Mn maintains its formal

154 Direct electron transfer would imply that alkali metal alkoxides are willing partners in these ele

155 oarenes with arenes, triggered by the use of alkali metal alkoxides in the presence of an organic add

156 o tune the properties of 2DESs by depositing alkali metal atoms.

157 isphosphite ligands combined with a suitable alkali metal BArF salt as a regulation agent (RA) provid

158 Shibasaki's rare earth alkali metal BINOLate (REMB) catalysts (REMB; RE = Sc, Y

159 Addition of alkali metal borates to 1 afforded the alkali metal disi

160 A series of alkali metal capped cerium(IV) imido complexes, [M(solv)

161 s of amides involving the direct coupling of alkali metal carboxylate salts with amines is described.

162 ed, enabled by tunable hemilability based on alkali metal cation binding with a macrocyclic "pincer-c

163 nd, the results suggest that the size of the alkali metal cation can control the number of Fe atoms t

164 se observed with recently published diboryne/alkali metal cation complexes.

165 abeling) point to a bridging function for an alkali metal cation connecting the sulfonate anion and a

166 f "alkali control," where the presence of an alkali metal cation enables the reduction of N2 under mi

167 nown to be influenced by the identity of the alkali metal cation in the electrolyte; however, a satis

168 M.2 concentration and a strong effect of the alkali metal cation M(+).

169 r mild conditions, and then chelation of the alkali metal cation uncovers a highly reactive species t

170 d by the diastereomers when cationized by an alkali metal cation, [M + X](+) where X = Li, Na, K, and

171 Even capped with an alkali metal cation, poor orbital energy matching and ov

172 ond was observed with increasing size of the alkali metal cation.

173 etallic pocket, closely interacting with the alkali metal cation.

174 The effect of alkali metal cations (Li(+) , Na(+) , K(+) , Cs(+) ) on

175 mical calculations that encapsulation of the alkali metal cations in the cavity of 1 predominantly oc

176 functional theory calculations show that the alkali metal cations influence the distribution of produ

177 e molecule is found to encapsulate the light alkali metal cations Li(+) and Na(+) in the absence of a

178 nteractions and of cation/pi interactions of alkali metal cations with aromatic rings was conducted.

179 hly sensitive to increased concentrations of alkali metal cations, a situation that remains unexplain

180 Addition of neutral boranes, alkali metal cations, and an Fe(2+) complex increases th

181 twork of gamma-cyclodextrins (gamma-CDs) and alkali metal cations, can separate a wide range of benze

182 w that direct lipid bilayer translocation of alkali metal cations, Cl(-), and a charged arginine side

183 opensities of inorganic cations, such as the alkali metal cations, have received relatively little at

184 bute to the sensitivity of exomer mutants to alkali metal cations.

185 1 in 2 days, without the need for additional alkali metal cations.

186 This suggests the importance of the alkali metal chelating agent in the reversibility of din

187 ido complexes demonstrated the impact of the alkali metal counterions on the geometry of the [Ce hori

188 on of alkali metal borates to 1 afforded the alkali metal disilicon(0) borates 1M[BAr4] (M = Li, Ar =

189 a systematic investigation of the effects of alkali metal doping on the charge state and crystal fiel

190 nd with zinc enolates generated by quenching alkali metal enolates of esters with zinc chloride.

191 The use of zinc enolates, instead of alkali metal enolates, greatly expands the scope of the

192 presence of montmorillonite and other salts, alkali metal fluorides did not yield any detectable olig

193 bly to traditional halex fluorinations using alkali metal fluorides, which generally require temperat

194 Herein we demonstrate that the presence of alkali metal halide salts, in conjunction with low coppe

195 active CF3(-) adduct can be synthesized from alkali metal hydride, HCF3, and borazine Lewis acids in

196 Light alkali metal hydridotriphenylborates M[HBPh3] (M = Li, N

197 ectrocatalyst was assembled with a different alkali metal intercalated between two nanosheets (NS) of

198 The synthetic and crystal chemistry of alkali metal intercalation into PAHs differs from that i

199 Alkali metal intercalation into polyaromatic hydrocarbon

200 lectively determined KI compare to different alkali metal iodides: NaI, RbI, CsI; also investigation

201 ation of a supramolecular system "Pt complex-alkali metal ion"; the latter is supported by restoratio

202 4) that form discrete molecular species with alkali metal ions (M(+) = Li(+), Na(+), K(+)).

203 usters, was used to record depth profiles of alkali metal ions (Me(+)) within thin SiO2 layers.

204 d that differences in folding with different alkali metal ions observed at high concentration arise f

205 the positive mode involves the depletion of alkali metal ions via ion evaporation of metal ions solv

206 ion was achieved after adduct formation with alkali metal ions, however, and efficiency was shown to

207 reover, FeSe-based systems intercalated with alkali metal ions, NH3 molecules or organic molecules ar

208 ing models, no size dependence for the other alkali metal ions.

209 p system will accumulate SO4(2-), Cl(-), and alkali metal ions.

210 nt proline isomeric molecules complexed with alkali metal ions.

211 s common to prior research in the field with alkali metal nitrate molten salt electrolytes and operat

212 The solution phase alkali metal reduction of [8]annulenyl isocyanate (C8H7N

213 C) can be further improved threefold through alkali metal salt promotion treatment.

214 was evaluated using several inorganic salts (alkali metal salts of chloride) and a weak acid of commo

215 omposed of gamma-cyclodextrin (gamma-CD) and alkali metal salts--namely, CD-MOF.

216 vided a method to obtain rates of ligand and alkali metal self-exchange in the RE/Li frameworks, demo

217 ther with evidence for a mechanism involving alkali metal silylenoid intermediates.

218 tionalization catalysed by an Earth-abundant alkali metal species.

219 clear nitride, complete encapsulation of the alkali metal with cryptand provides the terminally bound

220 The alkali fullerides, A(3)C(60) (A = alkali metal) are molecular superconductors that undergo

221 ns (Ln=rare earth metal; A=anionic ligand; M=alkali metal) involving reduction of Sc(NR2 )3 with K in

222 mination of the known SHG active AMCO3F (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) m

223 ermore, the unique structures adopted by the alkali metal-cationized cis- and trans-proline variants

224 it was observed that the resolution between alkali metal-cationized cis- and trans-proline variants

225 ydride complexes, providing a high-yielding, alkali metal-free route to strongly activated early-meta

226 Alkali metal-oxygen batteries are of great interests for

227 aceted role in a variety of media, including alkali metal-sulfur batteries, aqueous solutions at high

228 pproach has been realized using a rare earth/alkali metal/1,1'-BINOLate (REMB) heterobimetallic frame

229 llowing in situ the reactions of solids with alkali metal/ammonia solutions, using time-resolved X-ra

230 Examples of hetero-alkali-metal amides, an increasingly important compositi

231 lectron doping through in situ deposition of alkali-metal atoms, angle-resolved photoemission spectra

232 novel ternary Zintl phase Li3NaGe2 comprises alkali-metal cations and [Ge2](4-) dumbbells.

233 nic frameworks (CD-MOFs) in a combination of alkali-metal cations.

234 olecular organometallic compounds with mixed-alkali-metal cluster cores, LiK5 and Li3 K3 , sandwiched

235 5a-o, and 6a-e using superbasic solutions of alkali-metal hydroxides in DMSO is described.

236 ntral five-membered ring, for binding of six alkali-metal ions.

237 c in that magnesiation can only work through alkali-metal mediation, these reactions add magnesium to

238 Like other alkali-metal pyroxenes with S > (1)/(2), NaMnGe(2)O(6) (

239 ped magnetometers (OPMs) based on lasers and alkali-metal vapor cells are currently the most sensitiv

240 ntly used as negative electrode material for alkali-metal-ion batteries, similar to its oxide analogu

241 Combining alkali-metal-mediated metalation (AMMM) and N-heterocycl

242 lated InsPs have a much greater affinity for alkali metals (Li(+) > Na(+) > K(+)) than quaternary amm

243 ere we describe its intercalation by several alkali metals (Li, K, Rb and Cs) and alkali-earth Ca.

244 tron reduction of [Co(II)((R)salophen)] with alkali metals (M = Li, Na, K) leads to either ligand-cen

245 ded a range of ammonium or imidazolium ions, alkali metals and coordination compounds.

246 abundance in the host rocks, such as carbon, alkali metals and halogens, illustrates a feedback betwe

247 Light alkali metals are generally most easily intercalated due

248 Alkali metals are inherent constituents of biofuels.

249 nces in the results obtained using different alkali metals as reductants (Na, K, Rb, Cs).

250 in which a neutral molecule binds the light alkali metals exclusively through cation-pi interactions

251 Different alkali metals like Na, Li and Rb were incorporated in CZ

252 The controlled reaction of Na and Cs, two alkali metals of different ionic sizes and binding abili

253 Anions play a crucial role in locking alkali metals on the interior of metal-organic capsules

254 can cause large electron transfer from light alkali metals such as Li to Cs, causing Cs to become ani

255 Our system uses the thermal excitation of alkali metals to transmit an encoded signal over long di

256 ity in materials obtained by the reaction of alkali metals with polyaromatic hydrocarbons, such as ph

257 apacity for Na but a high capacity for other alkali metals.

258 ntered cubic lattice, which is common to all alkali metals.

259 CSP of NaCl, alkali molybdates and V2 O5 with small concentrations of

260 The CVD operation reduced the active alkali of the waste from 0.66 to <0.01M and the moisture

261 tients presenting to EDs with a diagnosis of alkali or acid ocular burn, chemical conjunctivitis, or

262 allenging transformation typically requiring alkali or transition metal reagents and/or harsh conditi

263 Alkali- or acid-induced structural modifications in beta

264 These results demonstrate that alkali- or acid-treated beta-chitin retained high suscep

265 demonstrates the strong interaction between alkali ordering, displacement, and electronic and magnet

266 Alkali pre-treatment resulted in the highest values of s

267 Furthermore, blending of alkali-produced protein isolates and washed minces, resp

268 Rheological studies revealed that blending alkali-produced protein isolates before precipitation re

269 nt anode material used in chlorate and chlor-alkali production is the dimensionally stable anode (DSA

270 including commercial Hg releases from chlor-alkali production, waste incineration, and mining).

271 e and oxygen evolution in chlorate and chlor-alkali production.

272 ctors were increased for regulating specific alkali-responsive gene expression.

273 oportionation and formation of a low-density alkali-rich intermediate, followed by anionic comproport

274 s of the reaction products formed during the alkali roasting of niobium-tantalum bearing minerals wit

275 Alkali salts impose ionic, osmotic, and high pH stresses

276 For simple atoms, such as alkalis, scattering resonances are extremely well charac

277 o reveal key structural elements involved in alkali sensing, we developed an in vitro method to quant

278 ant, which is dominant species on the saline/alkali soil of northeast China.

279 ive oil/water mixtures (such as strong acid, alkali solution and salt-water environment) or a strong

280 us-phase CO2 capture system, namely the dual alkali solvent (DAS) system, has been developed.

281 that spiro-ionenes constitute a new class of alkali-stable anion-exchange polymers and membranes.

282 Ca(2+) signaling was activated to transmit alkali stress signals as inferred by the accumulation of

283 We discuss the role of alkali supplementation in CKD as it relates to retarding

284 the basis of fundamental research and small alkali supplementation trials, correcting metabolic acid

285 terventional studies, and potential harms of alkali therapy in CKD.

286 The dose of alkali to provide in this setting is unknown as well.

287 The alkali tolerance molecular mechanism in roots from halop

288 This increase in thermostability and alkali tolerance translates to a 4,000,000-fold improvem

289 All these provide new insights into alkali-tolerant mechanisms in roots.

290 2, was cloned from Suaeda salsa, a salt- and alkali-tolerant plant, which is dominant species on the

291 were examined on HLA-I beads, iBeads, acid-/alkali-treated beads, and T cells using HLA-I monoclonal

292 ated the reduction of swelling power for the alkali-treated CLWMS at pH 11 and 12.

293 ration gives the fused triazines, which upon alkali treatment afford the desired radicals.

294 Alkali treatment of bacterial cellulose was an effective

295 n of NaOH concentration (X1: 0.4-1.2 mol/l), alkali treatment time (X2: 6-30 h), enzyme concentration

296 s follows: NaOH concentration of 0.76 mol/l, alkali treatment time of 18 h, enzyme concentration of 5

297 MS) was slurried (40%, w/w) and subjected to alkali treatments of pH 9, 10, 11, and 12 at 40 degrees

298 Alkali treatments of phosphorylated cross-linked starche

299 anish-style green table olives (treated with alkali), which develop a more appreciated bright golden-

300 mage is not mediated by direct effect of the alkali, which is effectively buffered by the anterior se