CN108906092A - 一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 - Google Patents
一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 Download PDFInfo
- Publication number
- CN108906092A CN108906092A CN201810525563.0A CN201810525563A CN108906092A CN 108906092 A CN108906092 A CN 108906092A CN 201810525563 A CN201810525563 A CN 201810525563A CN 108906092 A CN108906092 A CN 108906092A
- Authority
- CN
- China
- Prior art keywords
- carbon
- solution
- composite material
- ternary heterojunction
- carbon spheres
- 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.)
- Granted
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 63
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 61
- 239000002131 composite material Substances 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 239000000975 dye Substances 0.000 claims abstract description 22
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000000243 solution Substances 0.000 claims abstract description 18
- 125000002091 cationic group Chemical group 0.000 claims abstract description 14
- PLKATZNSTYDYJW-UHFFFAOYSA-N azane silver Chemical compound N.[Ag] PLKATZNSTYDYJW-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000001027 hydrothermal synthesis Methods 0.000 claims abstract description 11
- 101710134784 Agnoprotein Proteins 0.000 claims abstract description 10
- 235000011114 ammonium hydroxide Nutrition 0.000 claims abstract description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims abstract description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims abstract description 6
- 239000008103 glucose Substances 0.000 claims abstract description 6
- 239000011259 mixed solution Substances 0.000 claims abstract description 6
- 239000002105 nanoparticle Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 6
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 claims description 5
- 229960000907 methylthioninium chloride Drugs 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims 1
- 230000001699 photocatalysis Effects 0.000 description 13
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 238000001179 sorption measurement Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000003575 carbonaceous material Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000007146 photocatalysis Methods 0.000 description 3
- 230000032900 absorption of visible light Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 2
- 229940012189 methyl orange Drugs 0.000 description 2
- 238000013033 photocatalytic degradation reaction Methods 0.000 description 2
- 238000003917 TEM image Methods 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910021389 graphene Inorganic materials 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
- B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
- B01J27/1802—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates
- B01J27/1817—Salts or mixtures of anhydrides with compounds of other metals than V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, e.g. phosphates, thiophosphates with copper, silver or gold
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/39—Photocatalytic properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/51—Spheres
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/308—Dyes; Colorants; Fluorescent agents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/36—Organic compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/38—Organic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/40—Organic compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2305/00—Use of specific compounds during water treatment
- C02F2305/10—Photocatalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Toxicology (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Catalysts (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
本发明公开了一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法,将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应5‑8h得到平均直径为0.3‑0.7μm的碳球;将10wt%‑25wt%的氨水溶液滴加至0.05‑0.2mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为0.01‑0.1:1,搅拌2‑10h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3‑的摩尔比为3:1‑10,反应1‑3h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/碳球三元异质结复合材料。本发明能够实现快速高效去除阳离子染料的目的,合成的Ag3PO4@Ag/碳球三元异质结复合材料具有很好的稳定性。
Description
技术领域
本发明属于复合光催化材料的合成技术领域,具体涉及一种选择性去除阳离子染料的 Ag3PO4@Ag/碳球三元异质结复合材料的制备方法。
背景技术
新型光催化剂Ag3PO4具有良好的可见光催化性能,在可见光下(λ>420nm)光解水制O2时量子效率可达90%且可有效降解有机染料,是一种很有发展前景的光催化剂。但是由于Ag3PO4的导带位置比H2O/H2的氧化还原电位更正,导致光催化过程中H2O分子无法捕获光生电子,这些光生电子将与Ag3PO4中的Ag+发生反应生成金属Ag分布在Ag3PO4的表面,出现光腐蚀现象,影响Ag3PO4的光稳定性及光催化性能。
碳材料具有良好的导电性能,与Ag3PO4复合以后可以快速转移光生电子,增加Ag3PO4光催化性能的同时减少光腐蚀。金属Ag纳米颗粒也可以增加Ag3PO4中光生电子的转移及对可见光的吸收。将碳材料、Ag纳米颗粒同时与Ag3PO4复合可以进一步提高其光催化性能和光稳定性,已有文献报道Ag3PO4与碳材料(石墨烯、碳纳米管等)、Ag纳米颗粒共同复合可进一步提高其光催化性能,但是Ag纳米颗粒一般分布在Ag3PO4表面上,过多的 Ag纳米颗粒会占据Ag3PO4表面上的活性位点影响其光催化性能,因此Ag纳米颗粒的负载位置对其光催化性能有一定的影响。本申请采用化学沉淀法合成一种Ag3PO4@Ag/碳球三元异质结,其中Ag纳米颗粒分布在碳球上,碳球镶嵌在Ag3PO4中,这样既可以加速光生电荷的分离又不影响Ag3PO4光催化性能的发挥。
另外,利用异质结材料的吸附和光催化协同效应可以更有效的去除有机染料。在去除过程中,染料可以先从液相转移到固相催化剂,然后在光催化过程中染料被催化降解实现吸附位点的原位再生,提高了染料的去除效率。目前虽有一些异质结材料利用吸附光催化去除有机染料的报道,但是尚未见关于Ag3PO4@Ag/碳球三元异质结复合材料选择性去除阳离子染料的报道。
发明内容
本发明解决的技术问题是提供了一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法,含有Ag纳米颗粒的碳球不仅能够选择性地吸附阳离子染料,而且能够增加Ag3PO4对可见光的吸收以及加快光生电子的快速转移,最终实现快速高效去除阳离子染料的目的,合成的Ag3PO4@Ag/碳球三元异质结复合材料具有很好的稳定性。
本发明为解决上述技术问题采用如下技术方案,一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法,其特征在于具体步骤为:将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应5-8h得到平均直径为 0.3-0.7μm的碳球;将10wt%-25wt%的氨水溶液滴加至0.05-0.2mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为 0.01-0.1:1,搅拌2-10h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3-的摩尔比为3:1-10,反应1-3h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/ 碳球三元异质结复合材料。
本发明制得的Ag3PO4@Ag/碳球三元异质结复合材料中Ag纳米颗粒分布在碳球上,碳球镶嵌在Ag3PO4中,减少对Ag3PO4活性位点的覆盖,加速光生电子的转移,能够实现对阳离子染料亚甲基蓝的选择性去除。
本发明与现有技术相比具有以下优点:
1、Ag纳米颗粒直接生长在碳球上,碳球镶嵌在Ag3PO4中,减少对Ag3PO4活性位点的覆盖,加速光生电子的转移;2、室温下通过一步化学反应就可同时得到Ag纳米颗粒和Ag3PO4,不需要额外的光照和强还原剂还原得到Ag纳米颗粒;3、Ag3PO4@Ag/碳球三元异质结复合材料兼具吸附和光催化的性能,能够选择性去除阳离子染料亚甲基蓝,具有很好的稳定性。
附图说明
图1是实施例3制得的Ag3PO4@Ag/碳球三元异质结复合材料的SEM图,由图可以看出碳球镶嵌在Ag3PO4中;
图2是实施例2制得的Ag3PO4@Ag/碳球三元异质结复合材料的XRD图,由图可知样品中含有Ag3PO4和金属Ag;
图3是实施例2制得的Ag3PO4@Ag/碳球三元异质结复合材料的TEM图,由图可以看出Ag纳米颗粒分布在碳球上,碳球镶嵌在Ag3PO4中;
图4是Ag3PO4及实施例1和2制得的Ag3PO4@Ag/碳球三元异质结复合材料去除阳离子染料亚甲基蓝的效果图,由图可知制得的Ag3PO4@Ag/碳球三元异质结复合材料对亚甲基蓝具有很强的吸附和光催化降解效果;
图5是Ag3PO4及实施例1制得的Ag3PO4@Ag/碳球三元异质结复合材料去除阴离子染料甲基橙的效果图,由图可知制得的Ag3PO4@Ag/碳球三元异质结复合材料对甲基橙没有吸附效果,仅有光催化降解能力,进而表明本发明制得的制得的Ag3PO4@Ag/碳球三元异质结复合材料主要对阳离子染料具有良好的去除效果。
具体实施方式
以下通过实施例对本发明的上述内容做进一步详细说明,但不应该将此理解为本发明上述主题的范围仅限于以下的实施例,凡基于本发明上述内容实现的技术均属于本发明的范围。
实施例1
将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应5h得到平均直径为0.3μm的碳球;将25wt%的氨水溶液滴加至0.05mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为0.01:1,搅拌 6h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3-的摩尔比为3:2,反应3h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/碳球三元异质结复合材料,标记为Ag3PO4@Ag/碳球-1。
实施例2
将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应8h得到平均直径为0.7μm的碳球;将15wt%的氨水溶液滴加至0.1mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为0.03:1,搅拌 2h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3-的摩尔比为3:10,反应1h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/碳球三元异质结复合材料,标记为Ag3PO4@Ag/碳球-2。
实施例3
将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应8h得到平均直径为0.7μm的碳球;将10wt%的氨水溶液滴加至0.1mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为0.1:1,搅拌10h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3-的摩尔比为3:1,反应2h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/碳球三元异质结复合材料,标记为Ag3PO4@Ag/碳球-3。
以上实施例描述了本发明的基本原理、主要特征及优点,本行业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明书中描述的只是说明本发明的原理,在不脱离本发明原理的范围下,本发明还会有各种变化和改进,这些变化和改进均落入本发明保护的范围内。
Claims (2)
1.一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法,其特征在于具体步骤为:将摩尔浓度为0.5mol/L的葡萄糖溶液置于水热反应釜中于180℃水热反应5-8h得到平均直径为0.3-0.7μm的碳球;将10wt%-25wt%的氨水溶液滴加至0.05-0.2mol/L的AgNO3溶液中配制成透明的银氨溶液;将碳球加入到银氨溶液中,其中碳球与AgNO3的质量比为0.01-0.1:1,搅拌2-10h;将Na2HPO4溶液滴加到上述混合溶液中,其中Ag+与PO4 3-的摩尔比为3:1-10,反应1-3h,随后离心、过滤、洗涤,真空干燥箱中50℃干燥制得Ag3PO4@Ag/碳球三元异质结复合材料。
2.根据权利要求1所述的选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法,其特征在于:制得的Ag3PO4@Ag/碳球三元异质结复合材料中Ag纳米颗粒分布在碳球上,碳球镶嵌在Ag3PO4中,减少对Ag3PO4活性位点的覆盖,加速光生电子的转移,能够实现对阳离子染料亚甲基蓝的选择性去除。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810525563.0A CN108906092B (zh) | 2018-05-28 | 2018-05-28 | 一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810525563.0A CN108906092B (zh) | 2018-05-28 | 2018-05-28 | 一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN108906092A true CN108906092A (zh) | 2018-11-30 |
CN108906092B CN108906092B (zh) | 2021-01-15 |
Family
ID=64419542
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810525563.0A Expired - Fee Related CN108906092B (zh) | 2018-05-28 | 2018-05-28 | 一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108906092B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112058285A (zh) * | 2020-09-17 | 2020-12-11 | 安庆师范大学 | 一种Ag/Ag3PO4/碳化树脂复合物的制备方法及应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090068462A1 (en) * | 2007-08-10 | 2009-03-12 | Chiao-Cheng Chang | Nanosilver porous material particles and fabricating method thereof |
CN103120930A (zh) * | 2012-11-28 | 2013-05-29 | 江苏大学 | 一种微纳结构多功能复合材料及其制备方法 |
CN105148957A (zh) * | 2015-09-22 | 2015-12-16 | 阜阳师范学院 | 一种具有光催化性能复合材料BiPO4/Ag3P04/CNTs的制备方法 |
CN106423229A (zh) * | 2016-09-13 | 2017-02-22 | 天津科技大学 | 一种碳球负载磷酸银光催化剂的制备方法 |
CN107694582A (zh) * | 2017-09-09 | 2018-02-16 | 华北理工大学 | 一种泡沫铜负载纳米磷酸银光催化材料的合成方法 |
-
2018
- 2018-05-28 CN CN201810525563.0A patent/CN108906092B/zh not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090068462A1 (en) * | 2007-08-10 | 2009-03-12 | Chiao-Cheng Chang | Nanosilver porous material particles and fabricating method thereof |
CN103120930A (zh) * | 2012-11-28 | 2013-05-29 | 江苏大学 | 一种微纳结构多功能复合材料及其制备方法 |
CN105148957A (zh) * | 2015-09-22 | 2015-12-16 | 阜阳师范学院 | 一种具有光催化性能复合材料BiPO4/Ag3P04/CNTs的制备方法 |
CN106423229A (zh) * | 2016-09-13 | 2017-02-22 | 天津科技大学 | 一种碳球负载磷酸银光催化剂的制备方法 |
CN107694582A (zh) * | 2017-09-09 | 2018-02-16 | 华北理工大学 | 一种泡沫铜负载纳米磷酸银光催化材料的合成方法 |
Non-Patent Citations (1)
Title |
---|
KAI SHEN ET AL.: ""Preparation of ternary Ag/Ag3PO4/g‐C3N4 hybrid photocatalysts and their enhanced photocatalytic activity driven by visible light"", 《CHINESE JOURNAL OF CATALYSIS》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112058285A (zh) * | 2020-09-17 | 2020-12-11 | 安庆师范大学 | 一种Ag/Ag3PO4/碳化树脂复合物的制备方法及应用 |
CN112058285B (zh) * | 2020-09-17 | 2022-12-02 | 安庆师范大学 | 一种Ag/Ag3PO4/碳化树脂复合物的制备方法及应用 |
Also Published As
Publication number | Publication date |
---|---|
CN108906092B (zh) | 2021-01-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Shi et al. | Enhanced visible-light-driven photocatalytic H2 evolution on the novel nitrogen-doped carbon dots/CuBi2O4 microrods composite | |
CN111672497B (zh) | 一种原位合成二氧化铈/石墨相氮化碳复合光催化材料的方法 | |
CN105251517B (zh) | 一种Fe掺杂卤氧铋纳米材料的制备方法 | |
CN108671924B (zh) | 一种纳米金属/碳复合材料及其制备方法和应用 | |
CN105478142B (zh) | 一种硫化铟介孔空心微球光催化剂及其制备方法和用途 | |
CN106311295A (zh) | 一种以石墨烯为载体磷掺杂的双金属纳米催化剂及在水合肼或甲酸分解制氢的应用 | |
CN103861621B (zh) | 一种Bi7O9I3/石墨烯复合可见光催化剂及其制备方法 | |
CN107537571B (zh) | 一种多壁碳纳米管基贵金属催化剂及其制备方法 | |
CN110227500A (zh) | 一种Cd1-xZnxS-Ni/MoS2复合光催化剂及其制备方法、应用 | |
CN106179398A (zh) | 一种硼氢化钠醇解制氢用钌钴合金催化剂及其制备方法 | |
CN103586048A (zh) | 一种纳米Pd磁性催化剂、制备及用于液相催化反应 | |
CN105032418B (zh) | 不同微观形貌Ag/ZnO‑碳球三元壳核异质结光催化剂的制备方法 | |
CN113751032B (zh) | 一种用于有机污染物光降解催化剂的制备方法和应用 | |
CN111569875A (zh) | 一种铜/多孔碳纳米棒材料、制备方法和应用 | |
CN103055896A (zh) | 一种磁性可回收石墨烯基贵金属复合纳米片催化剂、制备方法及应用 | |
CN108155392A (zh) | 一种还原氧化石墨烯负载Pd-M纳米复合催化剂的制备方法 | |
CN102945971A (zh) | 一种用于甲醇、乙醇及异丙醇燃料电池的钯金属纳米粒子催化材料、其制备方法及应用 | |
CN102921419A (zh) | 一种用于苯直接羟基化制备苯酚的纳米铜—石墨烯复合催化剂及其制备方法 | |
CN103657646A (zh) | 二氧化钛纳米管负载金纳米粒子的方法 | |
CN108906092A (zh) | 一种选择性去除阳离子染料的Ag3PO4@Ag/碳球三元异质结复合材料的制备方法 | |
Liu et al. | Enhanced photocatalytic removal of U (vi) from water using tea waste biochar/gC 3 N 4/MoS 2 Z-scheme composite: synthesis, performance, and mechanistic insights | |
Zhang et al. | AgBrO3/Few-Layer g-C3N4 Composites: A Visible-Light-Driven Photocatalyst for Tetracycline Degradation | |
CN110180542B (zh) | 一种二氧化钛/石墨烯/金属单质三元复合光催化材料及光还原制备方法 | |
CN110586137A (zh) | 一种含有Mn0.5Cd0.5S和Au负载型光催化剂的制备方法 | |
CN110629245A (zh) | 氮掺杂碳包覆铜镉硫化物催化剂光电还原co2方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20210115 Termination date: 20210528 |
|
CF01 | Termination of patent right due to non-payment of annual fee |