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Biological reduction preparing method of styrene epoxidized gold catalyst

A gold epoxidation and catalyst technology, which is applied in the field of biological reduction preparation of styrene epoxidation gold catalysts, can solve the problems of environmental pollution of halogen-containing wastewater, equipment corrosion, large energy consumption and material consumption, and achieve high reactivity, The effect of mild conditions in the reduction process

Inactive Publication Date: 2013-02-06
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although this method is relatively simple and mature, it will cause a large amount of energy consumption and material consumption, severely corrode the equipment, and the produced halogen-containing wastewater will cause serious pollution to the environment. ,2008)

Method used

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  • Biological reduction preparing method of styrene epoxidized gold catalyst
  • Biological reduction preparing method of styrene epoxidized gold catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Preparation of plant leaf extract: Accurately weigh 0.25g of Arborvitae leaf dry powder, add 25mL of deionized water, place in a constant temperature water bath shaker at 30°C, shake and extract at a speed of 150r / min for 1h, vacuum filter and take Filtrate and be settled to 25mL, obtain the concentration and be the extract of oriental cypress leaves of 10g / L.

[0027] Preparation of chloroauric acid aqueous solution: Accurately weigh 1 g of chloroauric acid solid powder, dissolve it in 30 mL of deionized water, and then use deionized water to make the volume to 50 mL, and the concentration of the obtained chloroauric acid aqueous solution is 48.56 mmol / L.

[0028] Catalyst preparation: Take 25 mL of the above extract, add 260 μL of chloroauric acid aqueous solution to it, sonicate at 30°C for 10 min, stir for 1 h, then add 0.5 g of TS-1 carrier, continue stirring for 1 h, and vacuum filter to obtain a solid After drying in vacuum at 50°C for 12h, the catalyst was activ...

Embodiment 2

[0033] Preparation of plant leaf extract: Accurately weigh 0.5g of Arborvitae leaf dry powder, add 50mL of deionized water, place in a constant temperature water bath shaker at 30°C, shake and extract at a speed of 150r / min for 2h, and take after vacuum filtration Filtrate and be settled to 50mL, obtain the concentration and be the extract of oriental cypress leaves of 10g / L.

[0034] Preparation of the catalyst: Take 50 mL of the above extract, add 520 μL of the chloroauric acid aqueous solution prepared in Example 1, ultrasonicate at 60° C. for 20 min, stir for 2 h, then add 0.5 g of TS-1 carrier, and continue stirring for 2 h After vacuum filtration, the resulting solid was vacuum-dried at 50° C. for 12 hours and then calcined and activated for 6 hours at 450° C. in an air atmosphere to obtain catalyst B.

[0035] Catalyst evaluation conditions are the same as in Example 1, and the catalytic reaction results are shown in Table 1.

Embodiment 3

[0037] Preparation of plant leaf extract: Accurately weigh 0.5g of Arborvitae leaf dry powder, add 50mL of deionized water, place in a constant temperature water bath shaker at 30°C, vibrate and extract at a speed of 150r / min for 1h, vacuum filter and take Filtrate and be settled to 50mL, obtain the concentration and be the extract of oriental cypress leaves of 10g / L.

[0038] Preparation of the catalyst: Take 50 mL of the above extract, add 520 μL of the chloroauric acid aqueous solution prepared in Example 1 to it, sonicate at 60° C. for 10 min, stir for 1 h, then add 0.5 g of TS-1 carrier, and continue stirring for 1 h After vacuum filtration, the obtained solid was vacuum-dried at 50° C. for 12 hours and then calcined and activated for 3 hours at 350° C. in an air atmosphere to obtain catalyst C.

[0039] Catalyst evaluation conditions are the same as in Example 1, and the catalytic reaction results are shown in Table 1.

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Abstract

The invention discloses a biological reduction preparing method of styrene epoxidized gold catalyst and relates to the field of styrene epoxidized gold catalyst. The biological reduction preparing method includes firstly, selecting plant leaves to dry, smash and screen to obtain dry plant leaf powder; secondly, mixing the dry plant leaf powder obtained in the first step with deionized water, placing the mixture in a water bath shaking bed to shake and extract, obtaining filtrate by vacuum filtration, and refrigerating extract liquid of the plant leaves for standby use after volume is metered; thirdly, adding chloroauric acid water solution into the extract liquid of the plant leaves obtained in the second step, ultrasonically mixing and then stirring to obtain gold colloid; and fourthly, adding titanium silicalite molecular sieve (TS-1) carriers into the gold colloid obtained in the third step, keeping stirring so that gold nano particles are loaded on the carriers, drying solids obtained by vacuum filtration to roast and activate, and obtaining the styrene epoxidized gold catalyst which is load type powder catalyst Au / TS-1.

Description

technical field [0001] The invention relates to a styrene epoxidation gold catalyst, in particular to a bioreduction preparation method of the styrene epoxidation gold catalyst. Background technique [0002] Styrene oxide (SO), also known as styrene oxide or phenyl oxirane, is a fine chemical that can be used as an epoxy resin diluent, flavor enhancer, UV-absorber and stabilizer, etc. It is also an important intermediate in organic synthesis, pharmaceutical industry, perfume industry, etc. (Journal of Catalysis, 2001, 204:64-70; Journal of Catalysis, 2004, 223: 236-239). Styrene oxide can prepare a variety of compounds with high added value through selective ring opening or reaction with other organic substances. In recent years, the demand at home and abroad has increased sharply, and the market prospect is broad. [0003] There are two traditional production methods of styrene oxide in industry: [0004] 1) Haloalcohol method, the oxygen source used in this method is oxy...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J29/89C07D303/04C07D301/12
Inventor 李清彪刘承杜明明詹国武朱婧黄加乐孙道华王海涛
Owner XIAMEN UNIV