CN104495972B - 硫化亚砷的应用 - Google Patents
硫化亚砷的应用 Download PDFInfo
- Publication number
- CN104495972B CN104495972B CN201410743232.6A CN201410743232A CN104495972B CN 104495972 B CN104495972 B CN 104495972B CN 201410743232 A CN201410743232 A CN 201410743232A CN 104495972 B CN104495972 B CN 104495972B
- Authority
- CN
- China
- Prior art keywords
- photocatalyst
- arsenous
- application
- organic dye
- sulfide
- 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.)
- Expired - Fee Related
Links
- 238000005987 sulfurization reaction Methods 0.000 title 1
- 239000011941 photocatalyst Substances 0.000 claims abstract description 27
- 239000003344 environmental pollutant Substances 0.000 claims abstract description 20
- 231100000719 pollutant Toxicity 0.000 claims abstract description 20
- UKUVVAMSXXBMRX-UHFFFAOYSA-N 2,4,5-trithia-1,3-diarsabicyclo[1.1.1]pentane Chemical compound S1[As]2S[As]1S2 UKUVVAMSXXBMRX-UHFFFAOYSA-N 0.000 claims abstract description 18
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229940043267 rhodamine b Drugs 0.000 claims abstract description 14
- 230000000694 effects Effects 0.000 claims abstract description 12
- 238000013033 photocatalytic degradation reaction Methods 0.000 claims abstract description 3
- 230000015556 catabolic process Effects 0.000 claims description 9
- 238000006731 degradation reaction Methods 0.000 claims description 9
- 238000011156 evaluation Methods 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract description 5
- 238000002360 preparation method Methods 0.000 abstract description 5
- 230000002349 favourable effect Effects 0.000 abstract description 3
- 239000004408 titanium dioxide Substances 0.000 abstract description 2
- 239000000975 dye Substances 0.000 description 14
- 230000001699 photocatalysis Effects 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 5
- 229910052785 arsenic Inorganic materials 0.000 description 4
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052958 orpiment Inorganic materials 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002398 materia medica Substances 0.000 description 2
- 238000007146 photocatalysis Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000003911 water pollution Methods 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229940052288 arsenic trisulfide Drugs 0.000 description 1
- 125000000223 arsonoyl group Chemical group [H][As](*)(*)=O 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000001144 powder X-ray diffraction data Methods 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
Classifications
-
- 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
-
- 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
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/04—Sulfides
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
Abstract
本发明公开了一种硫化亚砷的应用。硫化亚砷作为光催化剂降解有机染料污染物,从而拓宽了其应用范围。硫化亚砷光催化降解有机染料污染物如罗丹明B染料的活性明显高于二氧化钛P25,也高于高活性的Ag3PO4光催化剂。本发明的硫化亚砷光催化剂活性高、制备方法简单、制备条件温和,有利于推广应用。
Description
技术领域
本发明属于环境治理中的光催化技术领域,涉及硫化亚砷作为一种新型光催化剂在降解有机染料污染物中的应用。
背景技术
目前,全世界的印染产业规模不断扩大,该产业排出的大量有机染料污染物,已成为全世界水污染的重要来源。半导体光催化技术可在室温下直接利用太阳光将染料污染物高效地氧化降解或消除。因此,通过光催化技术,充分利用太阳光来降解染料污染物是目前水污染治理的一条有利途径。因紫外光只占太阳光总能量的4%左右,而可见光占46%左右,所以通过光催化技术利用太阳能的关键在于利用太阳光中的可见光。因此,能吸收可见光的光催化剂(简称可见光催化剂)在当今环境治理领域具有重要的应用前景。
因为光催化过程中高的光生载流子复合率,再加上能带结构的限制,可见光催化剂降解染料污染物的活性一般较低。文献(Z.Yi,et al.Nature Materials,2010,9,559–564)报道,Ag3PO4可作为光催化剂用于可见光下有机染料污染物的降解,其活性远高于BiVO4、AgBr、AgI和N-TiO2等常见的可见光催化剂。发展活性高于Ag3PO4的新型光催化剂,具有较大的挑战性。
硫化亚砷又名三硫化二砷,化学式为As2S3,为黄色结晶粉末,是雌黄矿石的主要成分。据《神农本草经》、《本草纲目》记载,雌黄曾作为一种中药,起到杀虫、解毒、消肿等作用。在现代,As2S3主要用于制造砷和含砷化合物。目前,尚未有专利和文献报道将As2S3作为光催化剂用于污染物的降解。
发明内容
本发明目的在于提供硫化亚砷(As2S3)在环境治理领域的一种新应用,从而拓宽其应用范围。
本发明的技术方案为:
一种硫化亚砷的应用,硫化亚砷作为光催化剂降解有机染料污染物,具体应用的步骤为:
(1)在室温(20-25℃)下,用可见光进行照射,以有机染料污染物为底物,以硫化亚砷为光催化剂进行光催化降解,;
(2)硫化亚砷光催化剂的活性评价:测定有机染料污染物的降解速率,以其完全降解所需的时间来衡量。
上述的硫化亚砷的应用,所述的有机染料污染物优选为罗丹明B。
上述的硫化亚砷的应用,所述的可见光的波长大于420nm。
本发明的有益效果在于:
(1)实验结果表明,As2S3的光催化活性明显高于商用二氧化钛P25,也高于高活性的Ag3PO4光催化剂,解决了现有光催化剂降解活性低的问题。
(2)本发明的As2S3光催化剂制备方法简单、制备条件温和,有利于推广应用。
附图说明
图1本发明实施例制备的As2S3光催化剂的SEM图。
图2本发明实施例制备的As2S3光催化剂的粉末XRD图。
图3为本发明实施例制备的As2S3光催化剂的UV-Vis DRS谱图。
图4为本发明实施例制备的As2S3,以及P25和Ag3PO4光催化剂降解罗丹明B染料的活性结果图。其中,C0为光催化剂加入前罗丹明B的初始浓度,即12.0mg/L,C为光催化过程中任一时刻下罗丹明B的浓度。
具体实施方式
下面是本发明As2S3应用研究的具体实施例,以下实施例旨在进一步详细说明本发明,而非限制本发明。
(1)As2S3的制备:
取2mL浓度为2.6mol/L的Na2HAsO3溶液与70mL去离子水混合,再加入2mL浓度为36wt%的盐酸,得到砷前驱体溶液;取1.9g的Na2S·9H2O溶于70mL的去离子水,得到硫前驱体溶液。在室温下,将砷前驱体溶液与硫前驱体溶液混合,避光搅拌2h后离心分离,得到沉淀。将沉淀在60℃下干燥5h,得到As2S3样品。
(2)As2S3的表征:
从图1可见,As2S3具有尺寸为1–20μm的无规则颗粒形貌。图2显示,As2S3样品的晶相与《粉末衍射卡片集》中JCPDS No.19-0084的标准As2S3晶相吻合,这说明As2S3样品成功制备。从图3可见,As2S3样品的吸收带边在550nm左右,这表明As2S3本质上是一种能吸收可见光的半导体,是一种潜在的可见光催化剂。
(3)As2S3作为光催化剂降解罗丹明B染料污染物的活性评价:
将所得As2S3样品以罗丹明B(难降解的代表性染料污染物)为降解底物,进行光催化活性评价,并将其活性结果与P25和Ag3PO4对比。
光催化活性测试方案为:将75mg光催化剂置于100mL浓度为12mg/L的罗丹明B溶液(盛装于500mL的敞口烧杯)中,室温下避光搅拌40min,使罗丹明分子在光催化剂表面达到吸附–脱附平衡。然后打开500W氙灯(PLS-SXE300、北京泊菲莱科技有限公司),用滤光片滤去波长低于420nm的光,罗丹明B溶液液面位于氙灯正下方,液面与灯管中心之间的距离为14cm。分别在不同时间点取样,离心分离后取上清液,将上清液稀释得到试样。用紫外分光光度计(Lambda 35、美国PerkinElmer公司)测定试样在553nm处的吸光度。最后根据浓度-吸光度标准曲线推算试样的罗丹明B浓度。
由图4可见,As2S3光催化剂在15min以内将罗丹明B完全降解,Ag3PO4完全降解需要25min,P25即使在120min内降解罗丹明B的效率也非常低。由此可见,As2S3光催化剂的活性明显高于P25和Ag3PO4。因此,As2S3是一种降解染料污染物的高活性可见光催化剂。
Claims (1)
1.一种硫化亚砷的应用,其特征在于,硫化亚砷作为光催化剂降解有机染料污染物,具体应用的步骤为:
(1)在室温下,用可见光进行照射,以有机染料污染物为底物,以硫化亚砷为光催化剂进行光催化降解;
(2)硫化亚砷光催化剂的活性评价:测定有机染料污染物的降解速率,以其完全降解所需的时间来衡量;
所述的有机染料污染物为罗丹明B;
所述的可见光的波长大于420nm。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410743232.6A CN104495972B (zh) | 2014-12-08 | 2014-12-08 | 硫化亚砷的应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410743232.6A CN104495972B (zh) | 2014-12-08 | 2014-12-08 | 硫化亚砷的应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN104495972A CN104495972A (zh) | 2015-04-08 |
CN104495972B true CN104495972B (zh) | 2016-08-17 |
Family
ID=52937452
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201410743232.6A Expired - Fee Related CN104495972B (zh) | 2014-12-08 | 2014-12-08 | 硫化亚砷的应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104495972B (zh) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1613750A (zh) * | 2004-09-24 | 2005-05-11 | 武汉大学 | 金属硫化物的制备方法 |
CN101863524A (zh) * | 2010-06-11 | 2010-10-20 | 苏州大学 | 一种光催化氧化降解含染料废水的方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5866752A (en) * | 1997-09-29 | 1999-02-02 | Goozner; Robert E. | Destruction of volatile organic carbons |
WO2010000798A1 (en) * | 2008-07-04 | 2010-01-07 | Unilever Plc | Waste water treatment |
US20140174905A1 (en) * | 2012-12-20 | 2014-06-26 | Sunpower Technologies Llc | Photo-catalytic systems for the production of hydrogen |
-
2014
- 2014-12-08 CN CN201410743232.6A patent/CN104495972B/zh not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1613750A (zh) * | 2004-09-24 | 2005-05-11 | 武汉大学 | 金属硫化物的制备方法 |
CN101863524A (zh) * | 2010-06-11 | 2010-10-20 | 苏州大学 | 一种光催化氧化降解含染料废水的方法 |
Also Published As
Publication number | Publication date |
---|---|
CN104495972A (zh) | 2015-04-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103920479B (zh) | 生物质改性TiO2可见光光催化剂的制备方法及其应用 | |
CN101195094B (zh) | 可见光活化的二氧化钛卟啉纳米复合催化剂及其制备方法 | |
CN103252244B (zh) | 一种可见光响应型氯氧铋光催化剂的制备及其应用方法 | |
CN106902846B (zh) | 一种中空TiO2/MoS2复合材料及其制备方法 | |
CN106238083A (zh) | 一种石墨相氮化碳/二氧化钛复合材料催化剂的制备方法 | |
CN107963655A (zh) | 混相介孔二氧化钛、制备方法及采用其光催化去除含砷有机污染物的处理方法 | |
CN103272647B (zh) | 一种用于染料脱色的纤维素基ZnO-CdS复合光催化剂的制备方法 | |
CN106044842A (zh) | 一种扇形羟基氟化锌的制备方法及其应用 | |
CN102380403A (zh) | 一种硫掺杂的二氧化钛可见光催化剂制备方法 | |
CN106890655A (zh) | 一种具有高效可见光催化活性的Ag/AgCl/CdWO4催化剂 | |
CN105944712B (zh) | 一种钼酸铈钠/三氧化钼复合光催化剂的制备方法 | |
CN104495972B (zh) | 硫化亚砷的应用 | |
CN106311211B (zh) | 锗酸锆的应用 | |
CN106542584A (zh) | 一种富缺陷氧化钴光催化剂的制备方法 | |
CN104069877B (zh) | 一种Fe4I3O24H15可见光催化剂的制备方法及应用 | |
CN106944038B (zh) | 一种Sb2MoO6光催化材料的制备方法及应用 | |
CN104402086B (zh) | 氧化汞的应用 | |
CN106315749B (zh) | 一种无定型光催化剂的应用 | |
CN106745348A (zh) | CeGeO4的应用 | |
CN105129904B (zh) | 硒化汞的应用 | |
CN106807408B (zh) | Ce(IO3)4的应用 | |
CN104984756B (zh) | 一种NF-Bi2O3-SBA可见光响应光催化剂及其制备方法和应用 | |
Rajamanickam et al. | Solar light assisted photocatalytic mineralization of an azo dye, sunset yellow by using CAC/TiO 2 composite catalyst | |
CN106345497A (zh) | 高碘酸锆的应用 | |
CN110227441A (zh) | 一种光催化剂及其制备方法和应用 |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160817 |
|
CF01 | Termination of patent right due to non-payment of annual fee |