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13 protocols using ammonia water

1

Synthesis of Silver Nanoparticles

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Folic acid, 2-Hydroxy-1-ethanethiol, and dimethyl sulfoxide (DMSO) were purchased from Tianjin Guangcheng Chemical Reagent Co., Ltd. (Tianjin, China); ethanol, ethyl acetate, sodium hydroxide, oleylamine (OA), isooctane, ascorbic acid, bis (2-ethylhexyl) sulfosuccinate sodium (AOT, 98.0%), and dithiothreitol (DTT) were obtained from Macklin reagents Co., Ltd. (Shanghai, China); and sodium borohydride, Polyvinylpyrrolidone (PVP), silver nitrate, 4-dimethylaminopyridine (DMAP), Dicyclohexylcarbodiimide (DCC), and ammonia water were purchased from Sinopharm Chemical Reagent Co., Ltd. (Tianjin, China). All reagents were analytically pure and were used as received.
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2

Synthesis of Luminescent Strontium-Doped Lanthanum Nitrate Phosphors

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La(NO3)3·6H2O was obtained from Damao Chemical Co. Ltd. (Tianjin, China); Sr(NO3)2, Mn(NO3)3 (50% aqueous solution) and ammonia water were purchased from Sinopharm Chemical Co. Ltd. (Shanghai, China); citric acid was obtained from Guangfu Technology Development Co. Ltd. (Tianjin, China); these reagents were of analytical reagent grade. LDPE (Kunlun 18D) was obtained from the National Petroleum Corporation (Daqing, China); ethylene-vinyl acetate copolymer (EVA,7470) was obtained from Formosa Plastics Co. LTD (Taiwan, China) and conductive carbon black (CB, VXC-72) was purchased from CABOT Co. LTD (Boston, MA, USA)
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3

Synthesis of SiO2 Nanospheres

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After mixing 9 ml of concentrated ammonia water (Sinopharm Chemical Reagent Co., Ltd, Shanghai, China) with a concentration of 28%, 16.25 ml of ethanol (Sinopharm Chemical Reagent Co., Ltd, Shanghai, China) and 24.75 ml of deionized water, magnetic stirring was performed (Scheme 1). Then, a mixture of 4.5 ml of tetraethyl orthosilicate (TEOS, AR, Sinopharm Chemical Reagent Co., Ltd, Shanghai, China) and 45.5 ml of ethanol was quickly poured into the prepared solution. The mouth of the reaction flask was sealed with plastic wrap and the reaction continued for two hours at room temperature. Then, SiO2 nanospheres were prepared through centrifugation and cleaned with ethanol.
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4

Dopamine-Alginate Synthesis Protocol

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The chemicals used in the study included dopamine hydrochloride (McLean Biochemical Technology Co., Ltd.), calcium chloride (Xilong Chemical Co., Ltd.), sodium alginate, iron(iii) nitrate nonahydrate (Aladdin), anhydrous methanol, anhydrous ethanol, nitric acid (Shanghai Lingfeng Chemical Reagent Co., Ltd.), ammonia water and sodium hydroxide (Sinopharm Group Chemical Reagent Co., Ltd.). All reagents were of analytical grade, and no further purification was required prior to use. The water used in the study was ultrapure water (Millipore, ≥18.2 MΩ cm, 25 °C).
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5

Synthesis of Inorganic Phosphates

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All starting chemicals were obtained commercially without further purification. Magnesium chloride hexahydrate (MgCl2·6H2O), sodium hydroxide (NaOH), sodium dihydrogen phosphate (NH4H2PO4), triammonium phosphate ((NH4)3PO4)), ammonia water (NH3·H2O), hydrochloric acid (HCl), and glucose are of analytical grade and purchased from Sinopharm Chemical Reagent Co., Ltd. The yeast extract and malt extract are of biotech grade and purchased from Oxoid Ltd. and BBI Life Sciences Ltd., respectively. Deionized water was used in all of the experiments.
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6

Synthesis of Hybrid Anode Materials

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Ethanol, N,N-dimethylformamide, sodium hydroxide, urea and ammonia water were sold by Sinopharm Chemical Reagent Co. Ltd. (China). Polyacrylonitrile (PAN), polyvinylpyrrolidone (PVP) and potassium stannate trihydrate (K2SnO3) were obtained from Shanghai Aladdin Biochemical Technology Co., Ltd. (China). Tetraethyl orthosilicate (TEOS) was sold by Sigma Aldrich (Shanghai) Trading Co., Ltd. The electrolyte solution with 1 M LiPF6/ethylene carbonate (EC)/diethyl carbonate (DMC)/ethyl methyl carbonate (EMC) (1 : 1 : 1 by volume) were purchased from Guangzhou Tinci Materials Technology Co., Ltd. (China).
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7

Graphite-based Composite Synthesis for Dye Adsorption

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Graphite (100 mesh, XFnano), ferric chloride hexahydrate (FeCl3·6H2O, Sinopharm), ethylene glycol (Sinopharm), polyethylene glycol (PEG 4000, Sinopharm), sodium acetate trihydrate (NaAc·3H2O, Sinopharm), tetraethyl orthosilicate (Sinopharm), poly(diallyldimethylammonium chloride) (PDDA, Sinopharm), 3-aminopropyl triethoxysilane (APTES, Sinopharm), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC, Sinopharm), n-hydroxysuccinimide (NHS, Sinopharm), ammonia water (28 wt.%, Sinopharm), hydrochloric acid (Sinopharm), lead nitrate [Pb(NO3)2, Sinopharm], methylene blue (MB, Sinopharm).
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8

Silica-Coated Aramid Fiber Pulp

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The para-aramid pulp with a length of 1.15 ± 0.05 mm was purchased from Cangzhou Zhongli New Material Technology Co., Ltd., Cangzhou, China and was produced from poly(p-phenylene terephthalamide) (PPTA) fibers like Kevlar of DuPont. The chemicals, including tetraethoxysilane (TEOS, m(SiO2) ≥ 28.4%), ethanol (EtOH, 99.7%), n-hexane (97.0%), hydrochloric acid (HCl, 36.5%) and ammonia water (NH3∙H2O, 26.5–28.5%), were purchased from Sinopharm Chemical Reagent Co., Ltd., Shanghai, China. Trimethylchlorosilane (TMCS, 98%) was bought from Shanghai Aladdin Biochemical Technology Co., Ltd., Shanghai, China. Deionized water (DI∙H2O) was prepared using an ultra-pure water machine (ECO-S, HHitech, Shanghai, China) and was used to prepare 0.1 M HCl (aq) and 0.5 M NH3·H2O (aq), respectively.
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9

Hydrothermal Synthesis of Co-Sn Oxide Nanoparticles

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The supports of CoxSn(1−x)O2 (x = 0, 0.1, 0.2, 0.3) were synthesized by the hydrothermal method and then processed by heat treatment. One gram of hexadecyl trimethylammonium bromide (Sinopharm, Shanghai, China) was dissolved in a mixture of 20 ml of ethanol (Sinopharm) and 20 ml distilled water. Then, significant amounts of tin chloride (Sinopharm) and cobalt acetate (Sinopharm) (molar ratio (Sn2+ + Co2+): CTAB = 1 : 1.05) were added to the above solution, and continuously stirred to get a homogeneous solution. A certain amount of ammonia water (Sinopharm) was added dropwise to the solution under vigorous stirring at room temperature. The Ph value of the solution was maintained at 9 and under stirring for 2 h. After it was stirred, the mixture was transferred to a stainless Teflon-lined 100 ml autoclave and kept at 180°C for 24 h in an oven. The resulting yellow precipitate was collected by centrifugation, washed with distilled water and ethanol several times to remove the impurities, and then dried in a vacuum oven at 60°C. The dried samples were processed under 350°C for 5 h in a muffle furnace. After cooling to room temperature, CoxSn(1−x)O2 nanoparticles were finally obtained.
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10

Comprehensive Lemon Metabolite Analysis

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Fresh lemons (Eureka, Anyue, Sichuan, China) were purchased from a local supermarket in Nanjing. A standard sample of Cyclohexanone (>99.9%; C6–C25) was purchased from Sigma-Aldrich Trading Co., Ltd. (Shanghai, China). Sodium chloride, amino acid standard, o-phthalaldehyde (OPA), acetonitrile, methanol, 3-mercaptopropionic acid, boric acid, potassium dihydrogen phosphate, petroleum ether (30–60 °C), absolute ethanol, phosphoric acid, hydrochloric acid, ammonia water, ether, pyrogallic acid, ethanol (95%), and other reagents were purchased from Sinopharm Chemical Reagent Co., Ltd. (Beijing, China).
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