Synthesis of environmentally relevant fluorinated surfactants - a review

被引:306
作者
Lehmler, HJ [1 ]
机构
[1] Univ Iowa, Dept Environm & Occupat Hlth, Coll Publ Hlth, Iowa City, IA 52242 USA
关键词
perfluorinated compounds; perfluorooctanesulfonate; perfluorooctanoate; fluorotelomer alcohols; properties; synthesis;
D O I
10.1016/j.chemosphere.2004.11.078
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In the past years there has been a growing interest in fluorinated persistent organic pollutants such as perfluorooctanesulfonic acid, perfluorooctanesulfonamides, perfluorinated carboxylic acids and fluorotelomer alcohols. Although these compounds have probably been present in the environment for many decades, we are only now beginning to realize that these environmental contaminants may have serious environmental and health effects. This article gives a stateof-the-art review of synthetic approaches that have been employed for the synthesis of these environmentally relevant fluorinated compounds. Perfluorooctanesulfonic acid derivatives, in particular, pose a problem because only a few perfluorooctanesulfonic acid derivatives are available from commercial sources-a fact that limits the ability of researchers worldwide to further study these compounds. Because of the limited literature available, this article also describes synthetic approaches for shorter chain homologues or perfluoroether analogues that can potentially be applied for the synthesis of perfluorooctanesulfonic acid derivatives. The preparation of typical starting materials for the synthesis of perfluorooctanesulfonic acid derivatives such as the perfluoroalkanesulfonyl fluorides and chlorides will be discussed. Subsequently, their conversion into relevant perfluoroalkane sulfortate salts (RFSO3M), sulfonamides (RFSO2NH2), N-alkyl sulfonamides (RFSO2NHR, R = alkyl), NN-dialkyl sulfonamides (RFSO2NR2, R = alkyl), sulfonamidoethanol (R(F)SO(2)NRCH(2)CH2OH, R = -H, -CH3 or -C2H5) and sulfonamidoacetates (RFSO2NRCH2CO2H, R = -H, -CH3 or -C2H5) will be described. Many perfluorinated carboxylic acids and fluorotelomer alcohols are available from commercial sources. The review of the synthesis of these two classes of fluorinated compounds includes a review of their industrial synthesis and the synthesis of relevant degradation products. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1471 / 1496
页数:26
相关论文
共 188 条
[1]   SYNTHESIS OF 2H,2H-PERFLUOROALKYL AND 2H-PERFLUOROALKENYL CARBOXYLIC-ACIDS AND AMIDES [J].
ACHILEFU, S ;
MANSUY, L ;
SELVE, C ;
THIEBAUT, S .
JOURNAL OF FLUORINE CHEMISTRY, 1995, 70 (01) :19-26
[2]   Mortality of employees of a perfluorooctanesulphonyl fluoride manufacturing facility [J].
Alexander, BH ;
Olsen, GW ;
Burris, JM ;
Mandel, JH ;
Mandel, JS .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2003, 60 (10) :722-729
[3]  
Ameduri B, 1997, TOP CURR CHEM, V192, P165
[4]   Interaction of a partially fluorinated heptadecanoic acid with diacyl phosphatidylcholines of varying chain length [J].
Arora, M ;
Bummer, PM ;
Lehmler, HJ .
LANGMUIR, 2003, 19 (21) :8843-8851
[5]  
Austin ME, 2003, ENVIRON HEALTH PERSP, V111, P1485, DOI 10.1289/ehp.6128
[6]  
Banks R.E., 1970, Fluorocarbons and Their Derivatoives
[7]  
Behr FE, 2001, J FLUORINE CHEM, V112, P369
[8]   N-BENZYLTRIFLAMIDE - A GENERALLY USEFUL MITSUNOBU REAGENT FOR AMINE SYNTHESIS [J].
BELL, KE ;
KNIGHT, DW ;
GRAVESTOCK, MB .
TETRAHEDRON LETTERS, 1995, 36 (47) :8681-8684
[9]   DESCRIPTION OF A PROCESS OF CATALYTIC PREPARATION OF PERFLUOROALKYL SULFONAMIDE BY THE ADDITION OF ETHYLAMINE TO A PERFLUOROALKYLSULFONIC ACID CHLORIDE [J].
BENEFICEMALOUET, S ;
BLANCOU, H ;
TEISSEDRE, R ;
COMMEYRAS, A .
JOURNAL OF FLUORINE CHEMISTRY, 1986, 31 (03) :319-332
[10]   Perfluorooctanoate, perflourooctanesulfonate, and N-ethyl perfluorooctanesulfonamido ethanol;: peroxisome proliferation and mitochondrial biogenesis [J].
Berthiaume, J ;
Wallace, KB .
TOXICOLOGY LETTERS, 2002, 129 (1-2) :23-32