CN103433001B - Preparation method of biomass arsenic adsorbing material - Google Patents

Preparation method of biomass arsenic adsorbing material Download PDF

Info

Publication number
CN103433001B
CN103433001B CN201310367023.1A CN201310367023A CN103433001B CN 103433001 B CN103433001 B CN 103433001B CN 201310367023 A CN201310367023 A CN 201310367023A CN 103433001 B CN103433001 B CN 103433001B
Authority
CN
China
Prior art keywords
arsenic
saccharomycete
peanut
peanut tendril
biomass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201310367023.1A
Other languages
Chinese (zh)
Other versions
CN103433001A (en
Inventor
蓝碧健
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Taicang Biqi New Material Research Development Co Ltd
Original Assignee
Taicang Biqi New Material Research Development Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taicang Biqi New Material Research Development Co Ltd filed Critical Taicang Biqi New Material Research Development Co Ltd
Priority to CN201310367023.1A priority Critical patent/CN103433001B/en
Publication of CN103433001A publication Critical patent/CN103433001A/en
Application granted granted Critical
Publication of CN103433001B publication Critical patent/CN103433001B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention belongs to the field of water treatment material and relates to a preparation method of biomass arsenic adsorbing material. The preparation method provided by the invention is as follows: peanut vine containing protein is modified, and the specific process comprises peanut vine cleaning, smashing, saccharomycetes treatment, cyclodextrin composition and the like. The biomass arsenic adsorbing material prepared by the invention has the following advantages: (1), chemical treatment is not involved, and the manufacturing process is green and environment-friendly; (2), the prepared biomass arsenic adsorbing material is purely natural and degradable; (3), saccharomycetes and cyclodextrin are fully used for playing the effects of chelating and absorbing pentavalent arsenic ions, and the adsorbing capacity of the pentavalent arsenic ions is promoted to 156 mg/g, that is, each gram adsorbing material can absorb 156 mg pentavalent arsenic ions, which is 8.5 times of activated carbon. The biomass arsenic adsorbing material prepared by the invention can be used for treating waste water containing arsenic ions, can be used for a drinking water device, and has a wide market prospect.

Description

A kind of preparation method of living beings arsenic adsorbent material
Technical field
The invention belongs to material for water treatment technical field, be specifically related to a kind of preparation method of living beings arsenic adsorbent material.
Background technology
Reparation problem by arsenic polluted underground water body has caused worldwide extensive research and concern.The minimizing technology of current Arsenic in Drinking Water mainly contains coagulation, absorption, ion-exchange and film method etc.Wherein absorption method becomes the prefered method of Removal of Arsenic in Drinking Water because method is simple, reliable for effect.Adsorbent common at present has containing iron adsorbent, containing aluminium adsorbent etc., the advantages such as adsorption capacity is large, effect of removing arsenic is good that they have, but is difficult to because cost is higher promote (water for industrial use and waste water, 2005,36 (6), 35-38).China is large agricultural country, and the region Drinking water endemic arsenism lesion of China mostly is economy and (does not owe) developed regions, resident's relative distribution, be unfavorable for central water supply, therefore applied cost biological material that is cheap, abundance takes remediation of high As drinking water and to have broad prospects (Agriculture of Anhui science in China, 2008,36 (20), 8801-8802).
Biomass cellulose is the abundantest polymeric biomaterial (ion-exchange and the absorption of nature, 2010,26 (2), 187-192), can with many metal ion-chelants, therefore be widely used in water treatment industry, arsenic ion in adsorbed water, there is specific area and greatly, easily form that hydrophilic environments, sorption and desorption speed are fast, power of regeneration strong, purify the advantages such as thorough.
Microorganism (as bacterium, saccharomycete, algae, fungi etc.) is also the environmentally friendly sorbing material of a class, and material is cheap and easy to get, has a wide range of applications in arsenic-adsorbing.Carry out physical or chemical treatment to material before use and can improve its absorption property, physical method generally has heat treatment, autoclaving, freeze drying etc., and chemical method comprises acid adding, adds alkali or organic reagent etc.Utilize the existence of the activity change arsenic of microorganism, trivalent As (III) ionic oxide formation is become pentavalent As (V) ion, then in conjunction with other chemical reagent (as active carbon etc.) to reach the effective absorption to arsenic.
Nutrition content in peanut tendril enriches, and measures according to analysis, and containing thick protein, the crude fat of 2%, the carbohydrate of 46.8% of 12.9% in the peanut vine viticula leaf of sprawl growth, the gross protein value wherein in peanut leaf is up to 20%.
Novelty of the present invention is: (1) utilizes peanut tendril to be rich in the feature of protein, it is used saccharomycete process, and the protein of peanut tendril entrusts one's child to the care of sb. a large amount of saccharomycete, has facilitation to the arsenic adsorption capacity improving peanut tendril; (2) cyclodextrin molecular and pentavalent As (V) ion have extremely strong compatibility, utilize the feature that the space of peanut tendril cell membrane and cyclodextrin match, cyclodextrin molecular is embedded in peanut tendril, further increases the adsorption capacity of peanut tendril to arsenic; (3) peanut vine prepared overgrows the adsorbance of material sorbing material to pentavalent arsenic ion up to 156mg/g, and namely every gram of sorbing material adsorbable 156mg pentavalent arsenic ion, is 8.5 times of active carbon.
Summary of the invention
The invention belongs to technical field of water treatment, relate to a kind of preparation method of living beings arsenic adsorbent material.The preparation method that the present invention proposes is by the modification of proteinaceous peanut tendril, and concrete technology comprises that peanut tendril is cleaned, pulverizes, saccharomycete process and cyclodextrin compound etc.Living beings arsenic adsorbent material prepared by the present invention has the following advantages: (1) does not relate to chemical treatment, and technical process is green, environmental protection; (2) the living beings arsenic adsorbent material pure natural prepared, degradable; (3) make full use of saccharomycete and cyclodextrin to the chelating of pentavalent arsenic ion, suction-operated, the adsorbance of pentavalent arsenic ion is promoted to 156mg/g, and namely every gram of sorbing material adsorbable 156mg pentavalent arsenic ion, is 8.5 times of active carbon.Living beings arsenic adsorbent material prepared by the present invention both can be used for industrial enterprise containing arsenic ion wastewater treatment, and also can be used for drinking water apparatus, produce market has a extensive future.
The preparation method of the living beings arsenic adsorbent material that the present invention proposes, is characterized in that:
1) clean peanut tendril: by the rinsing of peanut tendril, oven dry;
2) peanut tendril is pulverized: the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles;
3) saccharomycete process: the peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 48 ~ 64 hours in 20 ~ 40 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000;
4) cyclodextrin compound: the peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 60 ~ 90 minutes, takes out, and filters, is placed in drying box, in 20 ~ 40 DEG C of dryings 4 ~ 8 hours, obtains living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 0.3% ~ 1.5%.
Living beings arsenic adsorbent material is placed in arsenic-containing waste water, regulates solution ph to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorbs complete, filters, by detecting residual arsenic ionic weight in solution, obtain the arsenic ion adsorbance of Biomass arsenic adsorbent material.
The biological material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.Multiple circulation like this, until the arsenic ion adsorbance of living beings arsenic adsorbent material is less than 75% of first adsorbance.
Accompanying drawing explanation
Fig. 1 is the stereoscan photograph of living beings arsenic adsorbent material.
Detailed description of the invention
The invention is further illustrated by the following examples
Embodiment 1
Gathered in by peanut tendril, clean with running water, dry, the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles; Peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 48 hours in 20 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000; The peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 60 minutes, takes out, filter, be placed in drying box, in 20 DEG C of dryings 4 hours, obtain living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 0.8%.
0.2g living beings arsenic adsorbent material is placed in 150mL containing arsenic ion waste water, solution ph is regulated to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorb complete, filter, by detecting residual arsenic ionic weight in solution, the arsenic ion adsorbance obtaining Biomass arsenic adsorbent material is 129mg/g, i.e. every gram of adsorbable 129mg arsenic ion of sorbing material.
The sorbing material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.10 circulations like this, the arsenic ion adsorbance of living beings arsenic adsorbent material still reaches 98mg/g, is greater than 75% of first adsorbance.
Embodiment 2
Gathered in by peanut tendril, clean with running water, dry, the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles; Peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 64 hours in 40 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000; The peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 90 minutes, takes out, filter, be placed in drying box, in 40 DEG C of dryings 8 hours, obtain living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 0.3%.
0.2g living beings arsenic adsorbent material is placed in 150mL containing arsenic ion waste water, solution ph is regulated to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorb complete, filter, by detecting residual arsenic ionic weight in solution, the arsenic ion adsorbance obtaining Biomass arsenic adsorbent material is 156mg/g, i.e. every gram of adsorbable 156mg arsenic ion of sorbing material.
The sorbing material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.10 circulations like this, the arsenic ion adsorbance of living beings arsenic adsorbent material still reaches 124mg/g, is greater than 75% of first adsorbance.
Embodiment 3
Gathered in by peanut tendril, clean with running water, dry, the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles; Peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 56 hours in 30 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000; The peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 70 minutes, takes out, filter, be placed in drying box, in 30 DEG C of dryings 6 hours, obtain living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 1.5%.
0.2g living beings arsenic adsorbent material is placed in 150mL containing arsenic ion waste water, solution ph is regulated to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorb complete, filter, by detecting residual arsenic ionic weight in solution, the arsenic ion adsorbance obtaining Biomass arsenic adsorbent material is 143mg/g, i.e. every gram of adsorbable 143mg arsenic ion of sorbing material.
The sorbing material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.10 circulations like this, the arsenic ion adsorbance of living beings arsenic adsorbent material still reaches 115mg/g, is greater than 75% of first adsorbance.
Embodiment 4
Gathered in by peanut tendril, clean with running water, dry, the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles; Peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 60 hours in 20 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000; The peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 80 minutes, takes out, filter, be placed in drying box, in 40 DEG C of dryings 5 hours, obtain living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 1.2%.
0.2g living beings arsenic adsorbent material is placed in 150mL containing arsenic ion waste water, solution ph is regulated to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorb complete, filter, by detecting residual arsenic ionic weight in solution, the arsenic ion adsorbance obtaining Biomass arsenic adsorbent material is 153mg/g, i.e. every gram of adsorbable 153mg arsenic ion of sorbing material.
The sorbing material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.10 circulations like this, the arsenic ion adsorbance of living beings arsenic adsorbent material still reaches 122mg/g, is greater than 75% of first adsorbance.
Embodiment 5
Gathered in by peanut tendril, clean with running water, dry, the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles; Peanut tendril after pulverizing is mixed with saccharomycete (specification: 200U/mg) and deionized water, stirs 1 hour, place 50 hours in 40 DEG C, filter, dry, obtain the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000; The peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 90 minutes, takes out, filter, be placed in drying box, in 40 DEG C of dryings 6 hours, obtain living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 0.8%.
0.2g living beings arsenic adsorbent material is placed in 150mL containing arsenic ion waste water, solution ph is regulated to be 5 ~ 6, in 20 DEG C of absorption 6 hours, the concentration of arsenic in waste water ion is 50 ~ 1000mg/L, adsorb complete, filter, by detecting residual arsenic ionic weight in solution, the arsenic ion adsorbance obtaining Biomass arsenic adsorbent material is 111mg/g, i.e. every gram of adsorbable 111mg arsenic ion of sorbing material.
The sorbing material of above-mentioned arsenic-adsorbing ion is placed in the phosphoric acid solution 1 hour that concentration is 0.1M, filters, clean, dry, complete desorption process, obtain the living beings arsenic adsorbent material of regeneration; Again above-mentioned regrown material is placed in arsenic-containing waste water, carries out arsenic ion absorption.10 circulations like this, the arsenic ion adsorbance of living beings arsenic adsorbent material still reaches 88mg/g, is greater than 75% of first adsorbance.

Claims (1)

1. a preparation method for living beings arsenic adsorbent material, is characterized in that:
1) clean peanut tendril: by the rinsing of peanut tendril, oven dry;
2) peanut tendril is pulverized: the peanut tendril after clean is placed in pulverizer, and being ground into particle diameter is 20 ~ 60 object particles;
3) saccharomycete process: be that saccharomycete and the deionized water of 200U/mg mix by peanut tendril and the specification after pulverizing, stir 1 hour, in 20 ~ 40 DEG C of placements 48 ~ 64 hours, filtration, drying, obtains the peanut tendril of saccharomycete process; The weight ratio of wherein saccharomycete/peanut tendril/deionized water is 1/1000/2000;
4) cyclodextrin compound: the peanut tendril of saccharomycete process is placed in cyclodextrin aqueous solution 60 ~ 90 minutes, takes out, and filters, is placed in drying box, in 20 ~ 40 DEG C of dryings 4 ~ 8 hours, obtains living beings arsenic adsorbent material; Wherein, the mass concentration of cyclodextrin aqueous solution is 0.3% ~ 1.5%.
CN201310367023.1A 2013-08-21 2013-08-21 Preparation method of biomass arsenic adsorbing material Active CN103433001B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310367023.1A CN103433001B (en) 2013-08-21 2013-08-21 Preparation method of biomass arsenic adsorbing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310367023.1A CN103433001B (en) 2013-08-21 2013-08-21 Preparation method of biomass arsenic adsorbing material

Publications (2)

Publication Number Publication Date
CN103433001A CN103433001A (en) 2013-12-11
CN103433001B true CN103433001B (en) 2015-01-07

Family

ID=49686770

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310367023.1A Active CN103433001B (en) 2013-08-21 2013-08-21 Preparation method of biomass arsenic adsorbing material

Country Status (1)

Country Link
CN (1) CN103433001B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104402148B (en) * 2014-12-16 2016-09-14 马鞍山太时芯光科技有限公司 A kind of secondary utilization method cutting the cutting water produced during gallium arsenide chips
CN105498711A (en) * 2015-12-29 2016-04-20 淄博永辰环境影响评价有限公司 Heavy metal ion adsorbent for livestock and poultry breeding wastewater, preparation method of heavy metal ion adsorbent and adsorption technology
CN106492753A (en) * 2016-02-16 2017-03-15 朱小平 A kind of preparation method of arsenic adsorbent material
CN106430374A (en) * 2016-12-22 2017-02-22 郑州丽福爱生物技术有限公司 Heavy-metal sewage treating agent
CN106587198A (en) * 2016-12-22 2017-04-26 郑州丽福爱生物技术有限公司 Heavy metal environment-friendly type sewage treating agent and preparing method thereof
CN110732310A (en) * 2019-11-08 2020-01-31 安徽潜隆机电科技有限公司 gas mask environment-friendly chromium-free carbon and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103071462A (en) * 2013-02-28 2013-05-01 南京工业大学 Modified peanut shell Hg(II) adsorbent, and preparation method and application thereof
CN103230780A (en) * 2013-04-19 2013-08-07 湖北工业大学 Heavy-metal absorbent prepared from vinasse and preparation method for same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61136435A (en) * 1984-12-07 1986-06-24 Agency Of Ind Science & Technol Arsenic adsorbent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103071462A (en) * 2013-02-28 2013-05-01 南京工业大学 Modified peanut shell Hg(II) adsorbent, and preparation method and application thereof
CN103230780A (en) * 2013-04-19 2013-08-07 湖北工业大学 Heavy-metal absorbent prepared from vinasse and preparation method for same

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
High-performance liquid chromatography of diastereomeric flavanone glycosides in Citrus on a β-cyclodextrin-bonded stationary phase (Cyclobond I);Martin Krause et al.;《Journal of Chromatography》;19911231;第588卷;第41-45页 *
JP昭61-136435A 1986.06.24 *
利用稻秆去除饮用水中五价砷的研究;娄淑芳 等;《安徽农业科学》;20081231;第36卷(第20期);第8801-8802页 *
酵母菌对重金属离子吸附的研究;李明春 等;《菌物系统》;19981231;第17卷(第4期);第367-373页 *

Also Published As

Publication number Publication date
CN103433001A (en) 2013-12-11

Similar Documents

Publication Publication Date Title
CN103433001B (en) Preparation method of biomass arsenic adsorbing material
Yin et al. Biochar as an adsorbent for inorganic nitrogen and phosphorus removal from water: a review
Bhatti et al. Dynamic biosorption of Zn (II) and Cu (II) using pretreated Rosa gruss an teplitz (red rose) distillation sludge
CN102247799B (en) Method for removing humic acid in water by utilizing surfactant modified attapulgite
CN101805037B (en) Method for removing humic acid pollutants in water by magnetic chitosan particle
CN103433011B (en) Preparation method of wheat straw modified material for removing lead ions in waste water
CN103861866A (en) Fixed enrichment method for city life compost heavy metals through modified nanocarbon
CN103071461B (en) The preparation of xanthogenation loess adsorbent and application in the treatment of waste water
CN103432999B (en) A kind of preparation method of rice straw base chromium ion sorbing material
Hu et al. Kinetic and equilibrium of cefradine adsorption onto peanut husk
CN103611494A (en) Amido modified attapulgite clay adsorbent and method for preparing and adsorbing humic acid
CN104355350A (en) Method for removing phosphate by modified fly ash
CN104128161B (en) A kind of amino modified activated coke heavy metal absorbent and preparation method thereof
CN104261570A (en) Livestock and poultry breeding anaerobic wastewater purifying agent
CN103111266B (en) Preparation method of granular adsorbent for removing antibiotics in water, prepared adsorbent and application thereof
CN109012598B (en) Preparation method of ciprofloxacin adsorption purifying agent based on manganese dioxide/graphene oxide nanocomposite
Li et al. Biosorption behaviors of biosorbents based on microorganisms immobilized by Ca-alginate for removing lead (II) from aqueous solution
CN100579648C (en) Process for preparing As-dispelling sorbent for sea-changed red mud porcelain granule and application method thereof
CN101337731A (en) Method for removing cadmium in industrial wastewater by bio adsorbing agent
CN101775081B (en) Modified quaternary ammonium salt of chitosan and application thereof
Kamarudzaman et al. Biosorption of iron (III) from aqueous solution using Pleurotus ostreatus spent mushroom compost as biosorbent
CN104773802B (en) A kind of composite flocculation agent aeroge of high absorption property and preparation method thereof
CN110193355A (en) The method that the porous material of pollution of chromium in water removal is removed in the modified Chinese parasol leaf production of CTAB
CN102886240B (en) Adsorbent for removing toxic element arsenic in water and application thereof
Zhang et al. Selection of optimum formulation for biosorbing lead and cadmium from aquatic solution by using PVA-SA’s immobilizing Lentinus edodes residue

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant