CN1019966C - Method of making active carbon from fruit shell of margosa - Google Patents

Method of making active carbon from fruit shell of margosa Download PDF

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Publication number
CN1019966C
CN1019966C CN89105254A CN89105254A CN1019966C CN 1019966 C CN1019966 C CN 1019966C CN 89105254 A CN89105254 A CN 89105254A CN 89105254 A CN89105254 A CN 89105254A CN 1019966 C CN1019966 C CN 1019966C
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CN
China
Prior art keywords
margosa
shell
active carbon
hours
liquor zinci
Prior art date
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Expired - Fee Related
Application number
CN89105254A
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Chinese (zh)
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CN1045751A (en
Inventor
曹先立
李金海
杜敏
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Individual
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Individual
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Publication date
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Priority to CN89105254A priority Critical patent/CN1019966C/en
Publication of CN1045751A publication Critical patent/CN1045751A/en
Application granted granted Critical
Publication of CN1019966C publication Critical patent/CN1019966C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/30Active carbon
    • C01B32/312Preparation
    • C01B32/342Preparation characterised by non-gaseous activating agents
    • C01B32/348Metallic compounds

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

The present invention relates to a method for producing active carbon, which adopts fruit shells of wild bead trees as raw materials, and then, the raw materials are soaked, carbonized and activated.

Description

Method of making active carbon from fruit shell of margosa
The invention belongs to the manufacture method of gac, in more detail, be to utilize the margosa shell to be raw material, by 10% liquor zinci chloridi soak, dry, 350 to 400 ℃ of charring furnace carbonizations, 1000 ℃ of activation furnace activation, pickling, washing, baking procedures carry out the method field that gac is made.
Margosa is a kind of wild plant, and only just there are more than 300 ten thousand strains in Cao County, Shandong Province, and annual result has 6,000 ten thousand to 8,000 ten thousand jin, never obtains utilizing.The margosa shell is hard, and dense structure can make the gac of porosity prosperity, because of containing making the useful Kuliansu of gac, is the good raw material of making top-grade active carbon in the margosa shell, but does not obtain development and use so far.
Purpose of the present invention is to utilize the margosa shell to make process of active carbon for raw material.
The present invention adopts following step to reach and realizes purpose of the present invention.A), in 10% liquor zinci chloridi, soaked 8 hours the margosa shell of pulverizing 40 mesh sieves.B) with the method for centrifugation, the margosa shell is separated with liquor zinci chloridi.C) dry margosa shell to water content naturally and be lower than 35%.D) the margosa shell was moved in 350 to 400 ℃ the carbide furnace carbonization 8 hours.E) the margosa shell after carbonization is transferred in 1000 ℃ the activation furnace, activates 10 to 15 hours, f) after the activated step, adopts the general same procedure of making gac, carries out pickling, washing, baking procedure.(pickling: will activate the charcoal material and immerse 10% hydrochloric acid soln, and heat to 60 ℃, and fully stir, ash content and impurity are all dissolved, washing: is 7 with 60 ℃ of boiling water flushing activation charcoal material to the pH value, centrifuge dripping activation charcoal material.Oven dry: the activation charcoal material after the dehydration, still contain 50% moisture, oven dry is 2 hours under 150 ℃ of temperature, is warming up to 600 ℃ then, keeps 4 hours again, is active carbon finished products after coming out of the stove.
In order to further specify the present invention, below for an embodiment:
Taking by weighing 100 kilograms of clean margosa shells by 40 mesh sieves soaks, separates, dries, after the carbonization, activation, pickling, washing, baking procedure, obtains 20 kilograms gac according to the step of introducing above of the present invention.
Utilize margosa shell production process of active carbon according to the present invention, its performance index are compared with standard index and are listed in the table 1
Table 1 is the synopsis of detected result of the present invention and standard index:
The test event standard detection
Index result
Adsorptive capacity (Asia
The blue absorption 〉=8 40 of methyl
Milliliter/gram)
Loss on drying % 50-60 50.9
Molten in the alcohol≤0.2 0.24
Separate thing %
Molten in the acid≤3 3.54
Separate thing %
Calcination is residual≤and 6 3.45
Slag %
Muriate %≤0.2 surpasses
0.2
Iron %≤0.10 surpasses
0.10
pH 4-7 5.5
Standard index in the table 1 is the Ministry of Chemical Industry of the People's Republic of China (PRC) that announces according to HG3-1290-80, gac, ministerial standard, detected result is the test event index that the present invention detects, the gac that utilizes the margosa shell to make as can be seen from Table 1, the main performance index adsorptive capacity is greater than ministerial standard.Gac constructed in accordance provides chemical plant, Jining, Shandong to do epoxy chloropropane discoloring agent usefulness, and effect is remarkable.
Therefore, provided by the present invention is a successful method with China tree shell manufacturing active carbon method.

Claims (1)

1) a kind of method of making charcoal alive is characterized in that comprising following several steps:
A) the margosa shell of pulverizing 40 mesh sieves was soaked 8 hours in 10% liquor zinci chloridi;
B) centrifugation margosa shell and liquor zinci chloridi;
C) dry margosa shell to water content naturally and be lower than 35%;
D) the margosa shell was moved in 350 to 400 ℃ the carbide furnace carbonization 8 hours;
E) the margosa shell after pyrolysis is transferred in 1000 ℃ the activation furnace, activates 10 to 15 hours;
F) after the activated step, the same procedure of useful general manufacturing gac is carried out pickling, washing, baking procedure.
2) according to claim 1, said manufacturing process of active carbon, the temperature that it is characterized in that liquor zinci chloridi among the step a are 30 to 40 ℃.
CN89105254A 1989-03-20 1989-03-20 Method of making active carbon from fruit shell of margosa Expired - Fee Related CN1019966C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN89105254A CN1019966C (en) 1989-03-20 1989-03-20 Method of making active carbon from fruit shell of margosa

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN89105254A CN1019966C (en) 1989-03-20 1989-03-20 Method of making active carbon from fruit shell of margosa

Publications (2)

Publication Number Publication Date
CN1045751A CN1045751A (en) 1990-10-03
CN1019966C true CN1019966C (en) 1993-03-03

Family

ID=4856021

Family Applications (1)

Application Number Title Priority Date Filing Date
CN89105254A Expired - Fee Related CN1019966C (en) 1989-03-20 1989-03-20 Method of making active carbon from fruit shell of margosa

Country Status (1)

Country Link
CN (1) CN1019966C (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100335408C (en) * 2005-07-19 2007-09-05 武汉理工大学 Production of active carbon with Chinese chestnut
CN101723361B (en) * 2009-12-31 2012-05-09 西北大学 Application of amygdalus pedunculata pall in preparation of active carbon
CN101838043B (en) * 2010-03-12 2011-09-21 重庆大学 Biological carbonaceous filler and preparation method thereof
CN102153080A (en) * 2011-03-29 2011-08-17 内蒙古农业大学 Yellowhorn shell activated carbon and preparation method thereof
CN106188925A (en) * 2016-08-09 2016-12-07 叶剑 A kind of polyphenylacetylene combination for clad plate and manufacture method thereof

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Publication number Publication date
CN1045751A (en) 1990-10-03

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