DOCSLIB.ORG

Selective Dissolution of Halide Perovskites As a Step Towards Recycling Solar Cells

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Selective Dissolution of Halide Perovskites As a Step Towards Recycling Solar Cells ARTICLE Received 5 Dec 2015 | Accepted 25 Apr 2016 | Published 23 May 2016 DOI: 10.1038/ncomms11735 OPEN Selective dissolution of halide perovskites as a step towards recycling solar cells Byeong Jo Kim1,*, Dong Hoe Kim2,*, Seung Lee Kwon1, So Yeon Park1, Zhen Li2, Kai Zhu2 & Hyun Suk Jung1 Most research on perovskite solar cells has focused on improving power-conversion efficiency and stability. However, if one could refurbish perovskite solar cells, their stability might not be a critical issue. From the perspective of cost effectiveness, if failed, perovskite solar cells could be collected and recycled; reuse of their gold electrodes and transparent conducting glasses could reduce the price per watt of perovskite photovoltaic modules. Herein, we present a simple and effective method for removing the perovskite layer and reusing the mesoporous TiO2-coated transparent conducting glass substrate via selective dissolution. We find that the perovskite layer can be easily decomposed in polar aprotic solvents because of the reaction between polar aprotic solvents and Pb2 þ cations. After 10 cycles of recycling, a mesoporous TiO2-coated transparent conducting glass substrate-based perovskite solar cell still shows a constant power-conversion efficiency, thereby demonstrating the possibility of recycling perovskite solar cells. 1 School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon 16419, Korea. 2 Chemistry and Nanoscience Center, National Renewable Energy Laboratory, Golden, Colorado 80401, USA. * These authors contributed equally to this work. Correspondence and requests for materials should be addressed to H.S.J. (email: [email protected]). NATURE COMMUNICATIONS | 7:11735 | DOI: 10.1038/ncomms11735 | www.nature.com/naturecommunications 1 ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms11735 he advent of perovskite solar cells (PSCs) has led to a capable of dissolving PSCs such that the Au electrodes and the change in the paradigm of emerging photovoltaic (PV) mp-TiO2-coated TCG substrates are separated through Ttechnology owing to the significant increase in their the dissolution of the perovskite layers. We find that the recycling power-conversion efficiency within the past 3 years1–3. Thus of PSCs can be realized based on the removal of trihalide far, the best reported efficiency, achieved by Seok and colleagues, perovskite materials and that a small amount of Pb residue has a is 22.1% (ref. 4). This efficiency is comparable to that of negligible effect on the ability to reuse the mp-TiO2-coated TCG other commercialized solar cells, such as multicrystalline Si substrate. The selective dissolution mechanism is attributable to (c-Si, 21.3%), cadmium telluride (CdTe, 22.1%) and copper the breaking down of the PbI6 octahedral frame in the trihalide indium gallium selenide (CIGS, 22.3%) solar cells4. However, to perovskite owing to the reaction between the partially facilitate commercialization of these emerging PVs, various issues positive Pb2 þ ions and a polar aprotic solvent. When the must be addressed, such as long-term stability, the need for regenerated electron-transport-layer-coated FTO glass (referred Pb-free perovskite light-absorbing materials, the economic to as the mp-TiO2-coated TCG substrate in this paper) is feasibility of the manufacturing process and an appropriate reused, the original power-conversion efficiency (15%) is retained ecofriendly disposal process for Pb-contained waste. The price of over 10 regeneration cycles. This study reveals the potential a Si solar module ranges from $0.6 to $1.0 per Wp (ref. 5), which impact of easily exchangeable PSCs, similar to electric batteries, is significantly higher than the target price of PSCs (lower than on the use of PSCs in various applications (for example, as $0.2 per Wp, see ref. 6). The target price for PV modules required portable power sources in wearable devices and internet-of-things to achieve grid parity, as determined by the United States devices). Department of Energy, is $0.5 per Wp; therefore, the target 7 figure ($0.2 per Wp) constitutes a paradigm-changing price . Results The competitive price of PSCs results from the low material Recycling procedure. Figure 1 shows the steps of the recycling cost and non-vacuum fabrication process of perovskite process for PSCs. After the deposition and annealing of the light absorbers. However, the relatively high material costs electron-transport layer, which is composed (in general) of for electron- and hole-transport materials, metallic electrode compact and mp-TiO2 layers, the MALI light absorber is coated materials (including gold or silver) and transparent conducting on the substrate. The hole-transport layer (HTL) and gold glass (TCG) substrate materials render realization of the target electrode are then deposited. During recycling, the MALI price difficult. For example, at the laboratory scale, the unit price perovskite and the HTL dissolve when the fabricated solar cell is of spiro-MeOTAD (2,2’,7,7’-tetrakis[N,N-di(4-methoxyphenyl) immersed in a polar aprotic solvent such as dimethylformamide amino]-9,9’-spirobifluorene), a widely used hole-transport (DMF), g-butyrolactone (GBL) or dimethyl sulfoxide (DMSO). material, is $200 per g (Lumtec). Gold, as a metallic electrode The resultant solution contains the recyclable gold electrode and material, and fluorine-doped tin oxide (FTO) glass cost $40 per g the mp-TiO -coated TCG substrate (Supplementary Fig. 1); the and approximately $10 per m2, respectively. As such, these 2 recycling procedure is shown in Supplementary Movie 1. After expensive materials account for 98% of the costs associated rinsing and drying of the selectively dissolved mp-TiO -coated with small, 1 inch  1 inch square devices. The price of 2 TCG substrate, the MALI layer, HTL and gold electrode are hole-conducting materials is expected to decrease by virtue of re-deposited to yield a recycled PSC. new synthesis technologies and large-scale synthesis methods. The effect of the polar aprotic solvent on the removal of the However, a significant reduction in the prices of gold and FTO MALI perovskite material was determined via field-emission glass seems unlikely; in fact, owing to limited mineral resources, scanning electron microscopy (FESEM). Figure 2a,b show their prices may vary significantly depending on global demand. plane-view images of the mp-TiO2 layer coated on the TCG The recycling of degraded PV modules has been considered as substrate and the MALI layer deposited on top of the mp-TiO an alternative approach to making PVs economically viable. In 2 layer, respectively. After selective dissolution processing of the particular, improvement of the long-term stability of PSCs is still MALI-coated substrate using DMF, the MALI layer is easily needed to compete with other types of solar cells, such as c-Si, removed and only the mp-TiO2 layer is observed (Fig. 2c). We CdTe and CIGS solar cells, which are being used in commercial determined the efficacy of this recycling process by repeatedly PV modules. However, considering the energy payback time recycling (in this work, we performed a total of 10 cycles) the (EPBT), which is the time required for a PV module to produce mp-TiO -coated TCG substrate of the PSC. The photocurrent an amount of energy comparable to that consumed during its 2 density–voltage (J–V) curve of a 10-times-recycled device is production, the EPBT of a perovskite PV module is 0.22 years, similar to that of a PSC based on a new substrate (Fig. 2d and which is the shortest nominal EPBT compared with all other Supplementary Fig. 2). These results indicate that PSCs can be competitors such as c-Si and CdTe (ref. 8). Therefore, if it were easily recycled. possible to recycle degraded perovskite PV modules, the issues inhibiting the commercialization of perovskite PV modules would be solved, such as their long-term stability, the production of Recycling mechanism. The selection of an appropriate solvent is large amounts of Pb-containing waste, the high unit cost of PSCs essential for an effective recycling process. To investigate the and the retrieval and reuse of expensive components such as gold, solvent effect, we immersed PSCs in non-polar and protic/aprotic silver and TCG. A shorter payback period of perovskite-based PV polar solvents. In the case of the non-polar solvents, only the modules compared with that of Si-based PV modules could be Au/HTL was removed from the Au/HTL/MALI/mp-TiO2/TCG realized via this process of recycling degraded PSCs. substrate, indicating that non-polar solvents selectively dissolve Therefore, in this paper, we introduce a recycling or repair the spiro-MeOTAD layer (Table 1 and Fig. 3). The perovskite methodology for PSCs. In this system, trihalide perovskite layer decomposed in both types of polar solvents, albeit with materials, such as methyl-ammonium lead iodide (CH3NH3PbI3, differing dissolution behaviours. This layer can dissolve in abbreviated as MALI) as well as formamidinium lead iodide hydrogen-bonded polar protic solvents, such as ethanol or water. (HC(NH2)2PbI3, abbreviated as FALI) and methyl-ammonium However, the dissolution kinetics is quite sluggish compared with lead bromide (CH3NH3PbBr3, abbreviated as MALBr) mixed the kinetics governing dissolution in a polar aprotic solvent. halides (in this study, (FALI)0.85(MALBr)0.15 was used), are When the PSCs were immersed in the polar protic solvents, the removed through a selective dissolution process. This process is perovskite layers became yellow in colour and, after more than 2 NATURE COMMUNICATIONS | 7:11735 | DOI: 10.1038/ncomms11735 | www.nature.com/naturecommunications NATURE COMMUNICATIONS | DOI: 10.1038/ncomms11735 ARTICLE ab Perovskite Deposition of ETL electron- FTO transport layer High-temp. annealing 100°C Re-formation of Rinsing and drying of perovskite layer selectively dissolved Formation of perovskite layer substrate Selective Polar aprotic Deposition of dissolution of hole-transport solvent failed PSC layer for recycling Peeled- metal electrode Au HTL Deposition of Au electrode Fabrication of PSCs Selective dissolution of PSCs Figure 1 | Recycling process for PSCs.
Load more

Recommended publications
  • The Role of Hydrogen Bonding in Paracetamol–Solvent and Paracetamol–Hydrogel Matrix Interactions
    materials Article The Role of Hydrogen Bonding in Paracetamol–Solvent and Paracetamol–Hydrogel Matrix Interactions Marta Miotke-Wasilczyk *, Marek Józefowicz * , Justyna Strankowska and Jerzy Kwela Insitute of Experimental Physics, Faculty of Mathematics, Physics and Informatics, University of Gda´nsk, Wita Stwosza 57, 80-308 Gda´nsk,Poland; [email protected] (J.S.); [email protected] (J.K.) * Correspondence: [email protected] (M.M.-W.); [email protected] (M.J.) Abstract: The photophysical and photochemical properties of antipyretic drug – paracetamol (PAR) and its two analogs with different substituents (acetanilide (ACT) and N-ethylaniline (NEA)) in 14 solvents of different polarity were investigated by the use of steady–state spectroscopic technique and quantum–chemical calculations. As expected, the results show that the spectroscopic behavior of PAR, ACT, and NEA is highly dependent on the nature of the solute–solvent interactions (non- specific (dipole-dipole) and specific (hydrogen bonding)). To characterize these interactions, the multiparameter regression analysis proposed by Catalán was used. In order to obtain a deeper insight into the electronic and optical properties of the studied molecules, the difference of the dipole moments of a molecule in the ground and excited state were determined using the theory proposed by Lippert, Mataga, McRae, Bakhshiev, Bilot, and Kawski. Additionally, the influence of the solute polarizability on the determined dipole moments was discussed. The results of the solvatochromic studies were related to the observations of the release kinetics of PAR, ACT, and NEA from polyurethane hydrogels. The release kinetics was analyzed using the Korsmayer-Peppas and Hopfenberg models.
    [Show full text]
  • Solvent Dependent Absorption and Fluorescence Ofaketocyanine Dye
    Indian Journal of Chemistry Vol. 34A, February 1995, pp. 94-101 Solvent dependent absorption and fluorescence of a ketocyanine dye in neat and binary mixed solvents Debashis Banerjee, Ashis Kumar Laha & Sanjib Bagchi" Department of Chemistry, Burdwan University, Burdwan 713 104, India Received 11 March 1994; revised and accepted 23 September 1994 The environmental effect on the ground and excited state properties of a ketocyanine dye has been studied by monitoring its absorption and fluorescence characteristics in various pure and bi- nary mixed solvents. The spectroscopic transition leading to the longest wavelength absorption or fluorescence has been found to involve considerable intramolecular charge transfer as evidenced by semiempirical MO calculations at the AMI level. Ground state complexation is indicated in protic solvents, aromatic hydrocarbons and cyclic ethers. The fluorescence maximum, E (F), shows a corre- lation with ET (30) scale of solvent polarity. A multiple linear correlation of E(F) with Kamlet-Taft parameter representing solvent dipolarity (n*) and hydrogen bonding ability (a and (3) suggests that apart from dipolar interactions specific solute-solvent interactions are important in determining flu- orescence maxima. Study of E (F) in mixed binary solvents points to a preferential solvation of the solute in the S 1 state. The polarity probes have found extensive applic- nine dye in pure and mixed binary solvents by ations during the last couple of years, especially monitoring its longest wavelength absorption and for the evaluation of various microenvironrnental fluorescence band. The dye chosen for the pre- properties 1-5. Although a large number of miCTOP- sent study is (1-1 ),(9-1)-di-l ,9-di-(2,3-dihydroindo- olarity reporters involving solvatochromic spectral lyl)- 4,6-dimethylene- nona-l,3,6,8-tetraene-5-one transition are known, e.g., 4-methoxycarbonylpyri- (Fig.
    [Show full text]
  • Acid Dissociation Constant - Wikipedia, the Free Encyclopedia Page 1
    Acid dissociation constant - Wikipedia, the free encyclopedia Page 1 Help us provide free content to the world by donating today ! Acid dissociation constant From Wikipedia, the free encyclopedia An acid dissociation constant (aka acidity constant, acid-ionization constant) is an equilibrium constant for the dissociation of an acid. It is denoted by Ka. For an equilibrium between a generic acid, HA, and − its conjugate base, A , The weak acid acetic acid donates a proton to water in an equilibrium reaction to give the acetate ion and − + HA A + H the hydronium ion. Key: Hydrogen is white, oxygen is red, carbon is gray. Lines are chemical bonds. K is defined, subject to certain conditions, as a where [HA], [A−] and [H+] are equilibrium concentrations of the reactants. The term acid dissociation constant is also used for pKa, which is equal to −log 10 Ka. The term pKb is used in relation to bases, though pKb has faded from modern use due to the easy relationship available between the strength of an acid and the strength of its conjugate base. Though discussions of this topic typically assume water as the solvent, particularly at introductory levels, the Brønsted–Lowry acid-base theory is versatile enough that acidic behavior can now be characterized even in non-aqueous solutions. The value of pK indicates the strength of an acid: the larger the value the weaker the acid. In aqueous a solution, simple acids are partially dissociated to an appreciable extent in in the pH range pK ± 2. The a actual extent of the dissociation can be calculated if the acid concentration and pH are known.
    [Show full text]
  • Fundamental Insights Into the Dissolution and Precipitation of Cellulosic Biomass from Ionic Liquid Mixtures
    Fundamental Insights into the Dissolution and Precipitation of Cellulosic Biomass from Ionic Liquid Mixtures By David L. Minnick Submitted to the graduate degree program in Chemical and Petroleum Engineering and the Graduate Faculty of the University of Kansas in partial fulfillment of the requirements for the degree of Doctor of Philosophy. ________________________________ Chairperson: Aaron M. Scurto ________________________________ Bala Subramaniam ________________________________ Raghunath V. Chaudhari ________________________________ Laurence Weatherley ________________________________ Belinda Sturm Date Defended: July, 14th 2016 The Dissertation Committee for David L. Minnick certifies that this is the approved version of the following dissertation: Fundamental Insights into the Dissolution and Precipitation of Cellulosic Biomass from Ionic Liquid Mixtures ________________________________ Chairperson: Aaron M. Scurto Date approved: July, 22nd 2016 ii Abstract Ionic liquids (ILs) are a unique class of molecular salts that melt at temperatures below 100oC. The ionic functionality of ILs provide this class of molecules numerous advantages for applications in reactions, separations, and materials processing due to their molecular flexibility through cation/anion selection. Additionally, ionic liquids possess negligible vapor pressures and may lead to more sustainable or “green” processes by eliminating solvent-based air pollution. For these reasons ionic liquids are being targeted for implementation in a range of industrial processes as sustainable solvent technologies. The primary objective of this dissertation targets the application of ionic liquids to cellulosic biomass processing. For instance, chemical processing of biomass remains a challenge as the rigid inter- and intra- molecular hydrogen bonding network of cellulose renders it insoluble in nearly all aqueous and organic solvents. Alternatively, select ionic liquids (ILs) are capable of dissolving significant quantities.
    [Show full text]
  • The Pennsylvania State University the Graduate School Department
    The Pennsylvania State University The Graduate School Department of Chemistry STUDY OF SOLVATION EFFECTS IN POLAR-PROTIC SOLVENTS USING COMPUTER SIMULATIONS A Thesis in Chemistry by Scot Richard Mente Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy May 1999 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. UMI Number: 9938021 UMI Microform 9938021 Copyright 1999, by UMI Company. All rights reserved. This microform edition is protected against unauthorized copying under Title 17, United States Code. UMI 300 North Zeeb Road Ann Arbor, MI 48103 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. We approve the thesis of Scot Richard Mente. Date of Signature Mark Maroncelli Professor of Chemistry Thesis Advisor Chair of Committee Professor of Vy/v Desjarlais Assistant Professor of Chemistry z/'+n 1 tong-Qing Associate Professor of Materials Science and Engineering f o si tin Peter C. Jurs( Professor of Chemistry Acting Head of the Department of Chemistry Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. ABSTRACT Computational chemistry techniques are used to study various aspects of solvation and solvent effects in polar-protic systems. A variety of methods have been utilized, including Monte Carlo and molecular dynamics simulations, as well as semi-empirical and ab initio calculations. The first part of this thesis examines the solvent catalyzed proton transfer reaction in 7-Azaindole and 1 -Azacarbazole. In Chapter 2 classical Monte Carlo and molecular dynamics simulations are used to examine the structure and dynamics of solvation of aza- aromatic solutes in alcohol and water solvents in an effort to determine whether the existing interpretations of the solvent participation in these reactions are reasonable.
    [Show full text]
  • Photochemical Processes Induced by the Irradiation of 4-Hydroxybenzophenone in Cite This: Photochem
    Photochemical & Photobiological Sciences PAPER Photochemical processes induced by the irradiation of 4-hydroxybenzophenone in Cite this: Photochem. Photobiol. Sci., 2015, 14, 2087 different solvents† Francesco Barsotti,a Marcello Brigante,*b Mohamed Sarakha,b Valter Maurino,a Claudio Mineroa and Davide Vione*a,c The singlet and triplet excited states of 4-hydroxybenzophenone (4BPOH) undergo deprotonation in the presence of water to produce the anionic ground-state, causing fluorescence quenching and photoactiv- ity inhibition. The same process does not take place in an aprotic solvent such as acetonitrile. In aceto- nitrile, 4BPOH is fluorescent (interestingly, one of its fluorescence peaks overlaps with peak C of humic substances), it yields singlet oxygen upon irradiation and induces the triplet-sensitised transformation of phenol (with a rate constant of (6.6 ± 0.3) × 107 M−1 s−1 (μ ± σ) between phenol itself and a triplet 4BPOH). The 4BPOH shows an intermediate behaviour in a partially protic solvent such as 2-propanol, where some deprotonation of the excited states is observed. In acetonitrile/2-propanol mixtures (at least up to 50% of 2-propanol) there is also some evidence of alcohol oxidation by the 4BPOH triplet state, Received 25th May 2015, while the experimental data are silent concerning such a possibility in pure 2-propanol. Considering that Accepted 23rd September 2015 benzophenones are important components of chromophoric dissolved organic matter (CDOM) in surface DOI: 10.1039/c5pp00214a waters, the present findings could have significance for the photoactivity of the hydrophilic surface layers www.rsc.org/pps vs. the hydrophobic cores of CDOM. 5 Introduction T1, which triggers important triplet-sensitised processes.
    [Show full text]
  • Kinetic Solvent Effects on 1,3-Dipolar Cycloadditions of Benzonitrile Oxide
    CORE Metadata, citation and similar papers at core.ac.uk JOURNAL OF PHYSICAL ORGANIC CHEMISTRY Provided by UniversityJ. Phys. of Org. Groningen Chem. Digital2005; Archive18: 908–917 Published online 13 April 2005 in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/poc.917 Kinetic solvent effects on 1,3-dipolar cycloadditions of benzonitrile oxide Theo Rispens and Jan B. F. N. Engberts* Physical Organic Chemistry Unit, Stratingh Institute, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands Received 21 December 2004; revised 7 February 2005; accepted 7 February 2005 ABSTRACT: The kinetics of 1,3-dipolar cycloadditions of benzonitrile oxide with a series of N-substituted maleimides and with cyclopentene are reported for water, a wide range of organic solvents and binary solvent mixtures. The results indicate the importance of both solvent polarity and specific hydrogen-bond interactions in governing the rates of the reactions. The aforementioned reactions are examples for which these factors often counteract, leading to a complex dependence of rate constants on the nature of the solvent. For the reactions of N- ethylmaleimide and N-n-butylmaleimide with benzonitrile oxide, isobaric activation parameters have been deter- mined in several organic solvents, water, and water–1-propanol mixtures. Interestingly, the activation parameters reveal significant differences in solvation in different solvents that are not clearly reflected in the rate constants. In highly aqueous mixtures, enforced hydrophobic interactions lead to an increase in rate constant, relative to organic solvents. However, the overall rate enhancement in water is modest, if present at all, because the solvent polarity diminishes the rate constant.
    [Show full text]
  • 8.4 Solvents in Organic Chemistry 339
    08_BRCLoudon_pgs5-1.qxd 12/8/08 11:05 AM Page 339 8.4 SOLVENTS IN ORGANIC CHEMISTRY 339 8.14 Label each of the following molecules as a hydrogen-bond acceptor, donor, or both. Indicate 1 the hydrogen that is donated1 or the atom that serves as the hydrogen-bond acceptor. (a) H Br (b) H F (c) O L 1 3 L 1 3 S3 3 H3C C CH3 L L 1 | (d) O 1 (e) (f) H3C CH2 NH3 S3 3 OH L L H3C C NH CH3 cL 1 L L L 8.4 SOLVENTS IN ORGANIC CHEMISTRY A solvent is a liquid used to dissolve a compound. Solvents have tremendous practical impor- tance. They affect the acidities and basicities of solutes. In some cases, the choice of a solvent can have dramatic effects on reaction rates and even on the outcome of a reaction. Understand- ing effects like these requires a classification of solvent types, to which Section 8.4A is devoted. The rational choice of a solvent requires an understanding of solubility—that is, how well a given compound dissolves in a particular solvent. Section 8.4B discusses the principles that will allow you to make general predictions about the solubilities of both covalent organic com- pounds and ions in different solvents. The effects of solvents on chemical reactions are closely tied to the principles of solubility. Solubility is also important in biology. For example, the solubilities of drugs determine the forms in which they are marketed and used, and such important characteristics as whether they are absorbed from the gut and whether they pass from the bloodstream into the brain.
    [Show full text]
  • Aprotic/Non Protonic Solvents Do Not Contains Ionizable Hydrogen Atom Are Called Non- Protonic Solvents
    L.S COLLEGE MUZAFFARPUR B. R. A. BIHAR UNIVERSITY Dr. Priyanka Department of Chemistry TOPIC:- classification of solvent UNIT 1: General classification of solvent 1.0 Introduction 2.0 Objectives Main content Classification of solvents 1) Acid solvent 2) Basic or protophilic solvent 3) Amphiprotic solvent 4) Protonic or protic solvent 5) Non protonic/aprotic solvent 6) Coordinating solvent 7) Inert solvent 1.0 Introduction Several bases exist for classifying solvents. For example, based on their content of hydrogen, solvents can be grouped into protic and aprotic solvents. Solvents may be classified based on their ability to accept or donate proton, according to their tendency to coordinate or based on their polarity. Which ever classification method is adopted is not conclusive because solvent classification method is done for convenience and several classification approach interwoven with each other. In this section, the various classifications are briefly considered. 2.0 Objectives of the study I. To understand what is acidic solvent II. To understand what is basic or protophillic solvent III. To understand what is amphiprotic solvent IV. To understand what is protonic/protic solvent V. To understand what is aprotic solvent VI. To understand what is coordinating solvent VII. To understand what is inert solvent Acidic solvents Solvents that have strong tendency to donate protons are called acidic solvent because they are acidic in nature Example are H2SO4,HF and CH3COOH. Basic or protophillic solvents Basic or protophillic solvents have strong tendency to accept protons and are basic in nature Examples are ammonia, hydrazine, ethylenediamine, etc Amphiprotic solvents Solvents which neither have a strong tendency to gain nor lose protons are called Amphiprotic solvents.
    [Show full text]
  • Effect of Protic Solvation in Organic Solution in Anion Exchange Extraction of Halide and Perchlorate Anions
    ANALYTICAL SCIENCES JUNE 1986, VOL. 2 293 Effect of Protic Solvation in Organic Solution in Anion Exchange Extraction of Halide and Perchlorate Anions Akira OHKI*, Xin-liang XIA0**, Yasumitsu FUJINO* and Makoto TAKAGI* *Department of Organic Synthesis , Faculty of Engineering, Kyushu University, Hakozaki, Fukuoka 812 **Department of Chemistry , Tianjin University, China The effect of organic solvents or additives was studied for the anion-exchange extraction reaction, (Q•Br)o+ (X-)w ~ (Q•X)o+(Br )W(Q+: liquid anion-exchanger; X: CI-,1 C104 subscripts o and w denote organic and aque- ous phases, respectively), with a special interest in the solvation of extracted anionic species by protic solvents or additives. The preference of extraction generally followed the order C104 >1->Br >CI-, whether the solvent is protic or aprotic. However, protic compounds such as phenols, alcohols, sulfonamides, carboxamides, and chlo- roform when used as solvent or additive showed a mitigating effect on such extraction preference. lipophilic phe- nols such as p-t-octylphenol (p-(1,1,3,3-tetramethylbutyl)phenol) and p-nonylphenol were especially efficient in enhancing the extractability of small (and thus hydrophilic) anions. The effect of substituents on the phenol was inves- tigated. o-Chlorination or o-bromination of p-t-octyl phenol lead to the increase of small-anion extractability. On the contrary, the 0-nitration considerably lowered the ability of phenolic compound in assisting the extraction of small anions. o,o'-Dibromination and o,o'-dimethylation lead to further lowering of such ability. The mechanism of protic solvation and its importance in determining the extraction selectivity among CI-, Br, 1-, and C104 - were discussed.
    [Show full text]
  • Electrochemistry in Nonaqueous Solutions Related Titles
    Kosuke Izutsu Electrochemistry in Nonaqueous Solutions Related Titles Endres, F., MacFarlane, D., Abbott, A. (eds.) Electrodeposition from Ionic Liquids 2008 ISBN: 978-3-527-31565-9 Eftekhari, A. (ed.) Nanostructured Materials in Electrochemistry 2008 ISBN: 978-3-527-31876-6 Hamann, C. H., Hamnett, A., Vielstich, W. Electrochemistry Second, Completely Revised and Updated Edition 2007 ISBN: 978-3-527-31069-2 Kosuke Izutsu Electrochemistry in Nonaqueous Solutions Second, Revised and Enlarged Edition The Author All books published by Wiley-VCH are carefully produced. Nevertheless, authors, editors, and Prof. Dr. Kosuke Izutsu publisher do not warrant the information contained 4-31-6-208 Kichijoji-honcho in these books, including this book, to be free of Musashino 180-0004 errors. Readers are advised to keep in mind that Japan statements, data, illustrations, procedural details or other items may inadvertently be inaccurate. Library of Congress Card No.: applied for British Library Cataloguing-in-Publication Data A catalogue record for this book is available from the British Library. Bibliographic information published by the Deutsche Nationalbibliothek The Deutsche Nationalbibliothek lists this publication in the Deutsche Nationalbibliografie; detailed bibliographic data are available on the Internet at http://dnb.d-nb.de. # 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim All rights reserved (including those of translation into other languages). No part of this book may be reproduced in any form – by photoprinting, microfilm, or any other means – nor transmitted or translated into a machine language without written permission from the publishers. Registered names, trademarks, etc. used in this book, even when not specifically marked as such, are not to be considered unprotected by law.
    [Show full text]
  • Experiment 9 – Chem 276 – Fall Semester 2010 Page 1 of 8
    Experiment 9 – Chem 276 – Fall Semester 2010 Page 1 of 8 Separation of compounds using acid-base extraction Introduction: Organic compounds are generally insoluble in water. Instead, they are soluble in organic solvents such as dichloromethane, chloroform, acetone, or diethyl ether. Highly polar molecules such as carbohydrates, or salts (or ionic , or charged, molecules), on the other hand, are usually soluble in water and insoluble in most organic solvents. These solubility properties are attributed to solvent polarity. Water is a polar and protic solvent which (as described by convenient rule of ‘like dissolves like’) is able to dissolve polar and charged compounds very well. Typical organic solvents are non-polar and aprotic (have no O-H or N-H bonds). These solvents are thus able to dissolve non-polar compounds and do not readily dissolve ions. Organic solvents are also usually immiscible with water. Thus, we can use the technique of extraction to separate water-soluble compounds from organic solvent-soluble compounds. By ‘ionizing’ organic acids and bases we can often convert them from water-insoluble to water- soluble, and thus, selectively remove them from an organic solvent using a straightforward extraction process. We can then re-form the organic compounds by protination and deprotination to reform the acids and bases respectively. At this point, if done correctly in a relatively small amount of water, solid organic acids and bases will precipitate in water and can be collected by simple filtration. In this experiment, your task is to use acid and base extraction to separate a mixture of three organic compounds: an acid, a base, and a neutral compound.
    [Show full text]