Relevant bibliographies by topics / Kanemite

Academic literature on the topic 'Kanemite'

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Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "Kanemite"

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Schmidmair, Daniela, Volker Kahlenberg, Daniel M. Többens, Herwig Schottenberger, Jochem De Wit, and Ulrich J. Griesser. "Temperature- and moisture-dependent powder X-ray diffraction studies of kanemite (NaSi2O4(OH)·3H2O)." Mineralogical Magazine 79, no. 1 (February 2015): 103–20. http://dx.doi.org/10.1180/minmag.2015.079.1.09.

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AbstractThe high-temperature- and moisture-dependent behaviour of synthetic kanemite (NaSi2O4(OH)·3H2O orSKS-10) has been studied byin situpowder X-ray diffraction. Heating experiments in the range between ambient temperatures and 250°C confirm earlier investigations that the dehydration of kanemite occurs in two steps. According to our results the two different reactions start at ∼30 and 75°C. The dehydration products have the following compositions: NaSi2O4(OH)·H2O (monohydrate) and NaSi2O4(OH), respectively. The crystal structures of both phases have been solved at ambient conditionsab initiofrom laboratory powder diffraction data using samples that have been carefully dehydrated at 60 and 150°C, respectively, and refined subsequently by the Rietveld method. Basic crystallographic data are as follows: NaSi2O4(OH)·H2O: orthorhombic, space groupPna21,a= 7.2019(1),b= 15.3252(2),c= 4.8869(1) Å,V= 539.37(1) Å3,Z= 4; NaSi2O4(OH): monoclinic, space groupP21,a= 6.3873(1),b= 4.8876(1),c= 7.1936(1) Å, β = 93.36(1)°,V= 224.19(1) Å3,Z= 2. Both compounds belong to the group of single-layer silicates based on Si2O4(OH) sheets. The sodium cations are located between the tetrahedral sheets and are surrounded by oxygen atoms from silicate anions and/or water molecules. Depending on the dehydration step the coordination numbers of the alkali ions vary between six (kanemite) and five (NaSi2O4(OH)). Kanemite and its two dehydration products show structural similarities which are discussed in detail. Moisture-dependent diffraction studies at ambient temperatures indicate that kanemite is stable between 10% and at least 90% relative humidity. Below the lower threshold a transformation to the monohydrate phase was observed. Dehydration and rehydration as a function of humidity is reversible. However, this process is combined with a significant loss of crystallinity of the samples.
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Michalik-Zym, Alicja, Małgorzata Zimowska, Elżbieta Bielańska, Krzysztof Bahranowski, and Ewa Serwicka. "Layered Sodium Disilicates as Precursors of Mesoporous Silicas. Part II: Hydration of δ-Na2Si2O5 and α-Na2Si2O5." Mineralogia 38, no. 2 (January 1, 2007): 161–70. http://dx.doi.org/10.2478/v10002-007-0024-7.

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Layered Sodium Disilicates as Precursors of Mesoporous Silicas. Part II: Hydration of δ-Na2Si2O5 and α-Na2Si2O5Reaction of δ-Na2Si2O5 and α-Na2Si2O5 with water at ambient conditions has been studied. The first substrate produced kanemite, the other a crystalline solid, assumed to be the layered hydrated α phase of yet unknown structure. Important differences have been observed in the kinetics of δ-Na2Si2O5 and α-Na2Si2O5 reactions with water, the phase transformation of the latter being distinctly slower. The observed different rates of hydration were associated with the different structural properties of the disilicates investigated. Hydrated δ-Na2Si2O5 and α-Na2Si2O5 possess, respectively, the platy and the needle-like morphology. Hydrated α-Na2Si2O5 contains less interlayer water, which is considered the reason for basal spacing being lower than that of kanemite. The interlayer water trapped between the layers of hydrated α-Na2Si2O5 is more strongly bound than that in kanemite.
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Serwicka, Ewa M., Krzysztof Bahranowski, Maciej Sitarz, Małgorzata Zimowska, and Alicja Michalik-Zym. "Retraction: Vibrational evidence for the “missing link” in structural kinship between kanemite and FSM-16 mesoporous silica." Dalton Transactions 45, no. 38 (2016): 15259. http://dx.doi.org/10.1039/c6dt90161a.

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Retraction of ‘Vibrational evidence for the “missing link” in structural kinship between kanemite and FSM-16 mesoporous silica’ by Ewa M. Serwicka, et al., Dalton Trans., 2016, DOI: 10.1039/C6DT01600F.
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Huang, Yining, Zhimei Jiang, and Wilhelm Schwieger. "A vibrational spectroscopic study of kanemite." Microporous and Mesoporous Materials 26, no. 1-3 (December 1998): 215–19. http://dx.doi.org/10.1016/s1387-1811(98)00270-4.

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Kimura, Tatsuo, Daigo Itoh, Nanae Okazaki, Mizue Kaneda, Yasuhiro Sakamoto, Osamu Terasaki, Yoshiyuki Sugahara, and Kazuyuki Kuroda. "Lamellar Hexadecyltrimethylammonium Silicates Derived from Kanemite." Langmuir 16, no. 20 (October 2000): 7624–28. http://dx.doi.org/10.1021/la000325t.

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Alba, María D., Pablo Chain, and Esperanza Pavón. "Synthesis and characterization of gallium containing kanemite." Microporous and Mesoporous Materials 94, no. 1-3 (September 2006): 66–73. http://dx.doi.org/10.1016/j.micromeso.2006.03.022.

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Branton, P. J., K. Kaneko, N. Setoyama, K. S. W. Sing, and Y. Fukusima. "Physisorption of Nitrogen by Mesoporous Modified Kanemite." Langmuir 12, no. 2 (January 1996): 599–600. http://dx.doi.org/10.1021/la950652e.

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Eypert-Blaison, C., F. Villiéras, L. J. Michot, M. Pelletier, B. Humbert, J. Ghanbaja, and J. Yvon. "Surface heterogeneity of kanemite, magadiite and kenyaite: a high-resolution gas adsorption study." Clay Minerals 37, no. 3 (September 2002): 531–42. http://dx.doi.org/10.1180/0009855023730056.

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AbstractThe surface properties of various synthetic layered silicates, Na-kanemite, Nakenyaite and magadiite, exchanged with H, K and Ca, were examined using high-resolution nitrogen and argon adsorption and the data were treated using the Derivative Isotherm Summation method. Using argon as an adsorbate, the aspect ratio of platelets can be determined. In the case of magadiite exchanged with various cations, the stacking of particles is influenced by the nature of the exchangeable cations, thicker platelets being observed for ions with low polarizability. Highresolution argon adsorption data also confirm some structural information previously deduced from Raman spectroscopy experiments concerning the existence of rather open six-membered rings at the surfaces of both magadiite and kenyaite. Furthermore, in the low-energy domain of the isotherms, argon forms a very organized film on basal planes, suggesting a commensurate relationship between silica framework and argon atoms for both magadiite and kenyaite, contrary to what is observed for kanemite. Nitrogen adsorption results reveal the presence of polar sites on the surface of all the investigated minerals but does not allow us to propose an unequivocal assignment for such sites.
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WIEKER, W., D. HEIDEMANN, R. EBERT, and A. TAPPER. "ChemInform Abstract: Chemistry of Kanemite (NaHSi2O5×3H2O)x." ChemInform 27, no. 2 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199602005.

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Apperley, David C., Michael J. Hudson, Matthew T. J. Keene, and James A. Knowles. "Kanemite (NaHSi2O5·3H2O) and its hydrogen-exchanged form." J. Mater. Chem. 5, no. 4 (1995): 577–82. http://dx.doi.org/10.1039/jm9950500577.

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Dissertations / Theses on the topic "Kanemite"

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Keene, Matthew T. J. "The structure of kanemite and some related compounds." Thesis, University of Reading, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339455.

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Superti, Guilherme Bicaleto. "Nanocompósitos polímero-aluminofosfatos (silicatos) lamelares = preparação, caracterização e propriedades." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250418.

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Orientadores: Heloise de Oliveira Pastore, Leonardo Marchese
Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química
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Resumo: Este trabalho descreve a síntese de dois materiais lamelares, um silicato, a magadiita, e um aluminofosfato, a AlPO-kanemita. No primeiro caso foi feita a substituição isomórfica com alumínio e no segundo com ferro ou vanádio e também se variou os tipos de alquilaminas no espaço interlamelar, alternandose cadeias longas e curtas. A magadiita foi convertida em sua forma ácida por dois métodos diferentes: um pela troca iônica com NH4+ e outro pela troca iônica com HCl. Estudos de DRX em temperaturas crescentes demonstraram que a estabilidade térmica da magadiita não se altera após a introdução de alumínio. A acidez dos materiais foi avaliada pelo monitoramento por FTIR do CO adsorvido e verificou-se que a introdução de alumínio produz sítios de alta acidez, comparável aos zeólitos. A comparação dos dois materiais ácidos diferentes indicou que os sítios produzidos por desamoniação são mais acessíveis ao CO do que os produzidos pela troca com HCl. A AlPO-kanemita foi utilizada na preparação de compósitos poliméricos por dois métodos diferentes, por mistura no estado fundido e polimerização in situ. No primeiro caso os polímeros usados, PP e EVA, não conseguem acessar o espaço interlamelar, enquanto que no segundo caso o PS e a PA6 tem acesso, mas este depende das aminas presentes no espaço interlamelar. As massas moleculares do PS não são afetadas pela presença da AlPO-kan, mas as da PA6 são drasticamente reduzidas. A introdução dos metais de transição tem efeito na decomposição térmica dos polímeros, produzindo uma maior quantidade de um material carbonáceo quando comparada aos análogos sem metal, o que diminui a inflamabilidade do material.
Abstract: This work describes the synthesis of two layered materials, magadiite and AlPOkanemite. The first is a silicate analogous to the natural hydrated layered silicate where isomorphous substitution with aluminum was performed. AlPO-kanemite is an aluminophosphate with the same structure as the hydrated layered silicate kanemite, from the same family as magadiita. It also passed by isomorphous substitution and was also synthesized with different alkylamines at its interlayer space, alternating short and long chains. Magadiite was converted in its acid form by two different methods: ion exchange with NH4+ and themolysis or by ion exchange with HCl. The diffractograms collected in crescent temperatures show that thermal stability of magadiite does not change after introduction of aluminum. The acidity of materials was measured by monitoring the CO adsorption with FTIR and the results shows that the acidity is high, comparable to zeolites. The comparison between the two different acid materials shows that the one produced by desamoniation has acid sites more accessible to probe molecules in respect to the one produced by exchange with HCl. AlPO-kanemite was used to produce polymeric composites by two methods: melt intercalation and in situ polymerization. In the first case the polymers (PP and EVA) were not able to access the interlayer space while at the second one the PS and PA6 were found in theinterlayer space, but their concentration depends on the quantities of the amines present at the material. The molecular mass of PS was not altered by the presence of the AlPO-kan but the PA6 is drastically reduced. The introduction of the metals has effect at thermal decomposition of the polymers, producing a larger quantity of a carbonaceous material when compared to its analogous, but without metals, that diminishes the flammability of the polymer.
Doutorado
Quimica Inorganica
Doutor em Ciências
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Oliveira, Vaeudo Valdimiro 1982. "Sílicas mesoporosas e silicatos lamelares contendo agentes organofuncionalizados : sorção e liberação controlada de fármacos." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250068.

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Orientador: Claudio Airoldi
Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química
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Resumo: Na presente investigação foram sintetizados os híbridos inorgânico-orgânicos micro/mesoestruturados: a) silicato lamelar do tipo kanemita sódica, b) sua forma quimicamente modificada com cobre e c) sílica mesoporosa SBA-16. A combinação dos reagentes Na2SiO3/NaOH/etanol e Na2SiO3/NaOH/Cu(NO3)2/etanol propiciaram a obtenção de kanemita sódica e sua forma contendo o cobre incorporado na estrutura inorgânica, através da substituição isomórfica do silício nas razões molares Si/Cu = 50, 100 e 200. Para as sílicas mesoporosas foram usados sistemas formados por copolímeros F127/TEOS/H2O, F127/TEOS/etanol/H2O e F127/TEOS/butanol/H2O em meio ácido. Os materiais organofuncionalizados previamente intercalado com dimetilsulfóxido (DMSO) e etilenodiamina (EN) formam os sólidos lamelares Na-KN-DMSO, Na-KN-EN e Cu-KN-EN, através do processo de pós-síntese com o agente sililante 3-iodopropiltrimetoxissilano, que reagiu subsequentemente com dietil iminodiacetato e benzidina, formando os híbridos mesoporosos. Os híbridos lamelares foram aplicados na sorção de metais e corantes em soluções aquosas. Dentre os cátions bário, cobalto e cobre, o cobre foi mais facilmente sorvido em Na-KN-EN quando comparado com Na-KN-DMSO. No caso dos corantes verde brilhante e azul reativo 15, o primeiro foi também mais eficiente na sorção. No processo de liberação de fármacos amoxicilina e omeprazol foram utilizados os híbridos mesoporosos. Os dados de liberação mostram que o primeiro fármaco apresentou uma cinética de liberação satisfatória no fluido intestinal simulado (FIS), enquanto que o omeprazol liberou em maior quantidade no fluido gástrico simulado (FGS)
Abstract: The present investigation deals with the syntheses of inorganic-organic nano/mesostrutered hybrids: a) sodic lamellar silicate kanemite, b) its chemically modified form with copper and c) SBA-16 mesoporous silicas. The reagents combination Na2SiO3/NaOH/ethanol and Na2SiO3/NaOH/Cu(NO3)2/ethanol enabled to obtain sodic kanemite and its synthesized form containing incorporated copper in the inorganic structure, through the isomorphic substitution of silicon using the molar ratio Si/Cu = 50, 100 and 200. For mesoporous silicas the copolymers F127/TEOS/H2O, F127/TEOS/ethanol/H2O and F127/TEOS/butanol/H2O in acidic condition were used. The synthesized organofunctionalized materials were previously intercalated with dimethylsulfoxide (DMSO) and ethylenediamine (EN) in the Na-KN-DMSO, Na-KN-EN and Cu-KN-EM lamellar solids, through the post-synthesis process with the silylating agent 3-iodopropyltrimethoxysilane, which subsequently reacted with diethyl iminodiacetate and benzidine. The lamellar hybrids were applied for cation and dye sorption processes. Among barium, cobalt and copper, the last cation was more favorable sorbed in Na-KN-EN, when compared with Na-KN-DMSO. In case of brilliant green and reactive blue 15 dyes, the first one was also more efficient in sorption. The controlled drug delivery process, amoxicillin and omeprazole were applied with mesoporous hybrid systems. The delivery data demonstrated that the first drug presented a satisfactory kinetic in the simulated intestinal fluid (SIF), while omeprazole presented high amount in the simulated gastric fluid (SGF)
Doutorado
Quimica Inorganica
Doutor em Ciências
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Corkery, Robert, and robert corkery@anu edu au. "Artificial biomineralisation and metallic soaps." The Australian National University. Research School of Physical Sciences and Engineering, 1998. http://thesis.anu.edu.au./public/adt-ANU20080124.190014.

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In this thesis, geometry is used as a basis for conducting experiments aimed at growing and arranging inorganic minerals on curved interfaces. Mineralisation is directed using crystalline and liquid-crystalline metallic soaps and surfactant/water systems as templates.¶ A review of the history, syntheses, structure and liquid crystallinity of metallic soaps and other amphiphiles is presented as a foundation to understanding the interfacial architectures in mesostructured template systems in general.¶ In this study, a range of metallic soaps of varying chain length and cation type are synthesised and characterised to find potentially useful templates for mineral growth. These include alkaline-earth, transition metal, heavy metal and lanthanide soaps. These are systematically characterised using a variety of analytical techniques, including chemical analyses, x-ray diffraction (XRD) infrared spectroscopy (IR) and differential scanning calorimetry (DSC). Their molecular and crystal structures are studied using transmission electron microscopy (TEM), cryo-TEM, electron diffraction (ED), electron paramagnetic spin resonance (EPR), absorption spectroscopy (UV-VIS), high resolution laser spectroscopy, atomic force microscopy (AFM), nuclear magnetic resonance spectroscopy, scanning electron microscopy (SEM), electron dispersive x-ray analysis (EDXA), thermal gravimetric analysis (TGA) and magnetic measurements. Models for the molecular and crystal structures of metallic soaps are proposed. The soaps are predominantly lamellar crystalline or liquid crystalline lamellar rotor phases with tilted and/or untilted molecular constituents. These display evidence of varying degrees of headgroup organisation, including superstructuring and polymerisation. A single crystal structure is presented for a complex of pyridine with cobalt soap. Simple models for their structure are discussed in terms of their swelling properties in water and oils. Experiments are also presented to demonstrate the sorbent properties of aluminium soaps on oil spills.¶ The thermotropic liquid crystallinity of alkaline earth, transition metal, heavy metal and lanthanide soaps is investigated in detail. This is done to assess their suitability as templates, and to document their novel thermotropic behaviour, particularly the relatively unknown lanthanide soaps. Liquid crystalline behaviours are studied using high-temperature XRD (HTXRD), hot-stage optical microscopy and DSC. Models for a liquid crystalline phase progression from crystals to anisotropic liquids are discussed in terms of theories of self-assembly and interfacial curvature. The terminology required for this is drawn from various nomenclature systems for amphiphilic crystals and liquid crystals. General agreement with previous studies is reported for known soaps, while liquid crystallinity is demonstrated in the lanthanide and some non-lanthanide soaps for the first time. A general phase progression of crystalline lamellar through liquid crystalline lamellar to non-lamellar liquid crystalline is discussed in terms of models concerned with the molecular and crystal structures of the soaps and their phase transitions via headgroup and chain re-arrangements.¶ Experiments aimed at guiding growth of metal sulfides using metallic soaps as templates are described, and a model for this growth is discussed. Metal sulfides have been successfully grown by reacting crystalline and liquid crystalline transition metal and heavy metal soaps with H2S gas at room temperature and at elevated temperature. These have been characterised using XRD, TEM, ED and IR. Sulfide growth is demonstrated to be restricted and guided by the reacting soap template architecture. Zinc, cadmium, indium and lead soaps formed confined nanoparticles within the matrix of their reacting soap template. In contrast, curved and flat sheet-like structures, some resembling sponges were found in the products of sulfided iron, cobalt, nickel, copper, tin and bismuth soaps. A model to explain this behaviour is developed in terms of the crystal and liquid crystal structures of the soaps and the crystal structures of the metal sulfide particles.¶ Liquid crystalline iron soaps have been subjected to controlled thermal degradation yielding magnetic iron oxide nanoparticles. Some XRD and TEM evidence has been found for formation of magnetic mesostructures in heat-treated iron soaps. Models for the molecular and liquid crystalline structure of iron soaps, their thermotropic phase progression and eventual conversion to these magnetic products are discussed. Systematic syntheses of mesoporous silicates from sheeted clays are discussed.¶The templates that have been used are cationic surfactants and small, organic molecular salts. Experiments are reported where a cooperative self-assembly of surfactant/water/kanemite plus or minus salt and oils yields 'folded sheet materials' (FSM'S). Templating of kanemite has also been achieved using cobalt cage surfactants. A theoretical prediction of the specific surface areas and specific volumes of homologous sets of FSM's gave excellent agreement with measured values. The geometry and topology of the mesostructures are discussed. A theoretical model is also discussed regarding the curvature found in the sheets of natural clays , and results of templating clays and silica using metallic soaps are presented. Experiments and a model for low temperature nucleation and growth of microporous silicalite-1 are described in terms of silica templating by water clathrates.¶ Finally, the problem of finding minimal surface descriptions of crystal networks is addressed. Combinatoric methods are used to disprove the existence of possible embeddings of type I and II clathrate networks in non-self intersecting periodic minimal surfaces. The crystal network of the clathrate silicate, melanophlogite is successfully embedded in the WI-10 self-intersecting surface. Details of a previously unreported, genus-25 periodic surface with symmetry Im3m are discussed.
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Chiang, Chia-Ching, and 江佳青. "Construction of the Sitar's Tradition in Taiwan:A Case Study of Its Player Ryohei Kanemitsu(Yo)." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/28841149680759207379.

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碩士
國立臺南藝術大學
民族音樂學研究所
100
After The Invention of Tradition was published in 1983 by the left-wing British historian E.J. Hobsbawm and T. Ranger, the meaning of “tradition” has been deconstructed by scholars in many other disciplines. It is prevailingly recognized that the tradition is represented as a non-fixed form and can be interpreted in different ways. In Taiwan, due to its people’s growing cultural exchanges with those in other countries, there have been more cultural practices associated with “exoticism.” Among those practices, we witness the presence of the Sitar, the music instrument belonging to the Northern Indian musical tradition, Hindustani. After the Sitar was adapted to Taiwanese local culture, it has developed its unique listening habitus and commercial mechanism, as well as new forms of “tradition.” As Hobsbawm says, the invention of tradition is a series of practices re-produced by men. This thesis thus focuses on the performance and teaching of the Sitar player, Ryohei Kanemistu (Yo), who plays Hindustani music in Taiwan. It begins with the exploration of the “tradition” Yo inherited, and then discusses how he has constructed a Sitar’s tradition after he moved to Taiwan in 2008. This thesis contains three facets. First is to examine the literature of Sitar music. Drawing from the history, teaching system, repertories, and performances of the Sitar, this thesis outlines its present-day tradition in northern India. Second is to observe the current situations of Indian music in Taiwan, in particular its practices, promotion, and institutionalization of both profit and non-profit organizations. Third is, by employing the ethnographic approach, to explore how Yo has constructed an environment and an image for Sitar through his teaching and performance. Then how he has connected himself to the tradition of Sitar that he inherits and how he has constructed a new tradition are also analyzed.
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Books on the topic "Kanemite"

1

Itoyama, Eitarō. Kanemōke tetsugaku. Tōkyō: Kanki Shuppan, 2002.

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Kanemata iseki (D chiku): Niigata-ken Nakakubiki-gun Myōkōkōgen-machi Kanemata iseki hakkutsu chōsa hōkoku. [Myōkōkōgen-machi]: Myōkōkōgen-machi Kyōiku Iinkai, 1986.

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Kanemi yushō: Owaranai shokuhin higai. Fukuoka-shi: Kaichōsha, 2010.

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Okayama-ken Kodai Kibi Bunkazai Sentā. Hyakkengawa Kanemoto iseki 3, Hyakkengawa Imadani iseki 3, Hyakkengawa Sawada iseki 4. Okayama-shi: Kensetsushō Okayama Kasen Kōji Jimusho, 1997.

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Yano Toyoko Tsuitō Bunshū Kankōkai. Yano Toyoko kaku ikitari: Aru Kanemi yushō higaisha no ayumi. Ōsaka-shi: Atto Wākusu, 2010.

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Murakami, Ryū. Ojiisan wa yama e kanemōke ni: Toki to shite tōshi wa kibō o umu. Tōkyō: Nippon Hōsō Shuppan Kyōkai, 2001.

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Shinkō shūkyō: Kanemōke to kenryoku arasoi no jittai : shūkyō to iu kakuremino o kita kyōdan no shōtai wa... 5th ed. Tōkyō: Seinen Shokan, 1987.

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Maiduguri, University of, ed. Aspects of economic development in Nigeria: Inaugural lecture delivered at the El-Kanemi Hall on Wednesday, 27 February 1985, University of Maiduguri. [Maiduguri, Nigeria]: University of Maiduguri, 1985.

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Dan, Isao. Shinko shukyo: Sono kyoki to fuhai : Shinjadamashi to kanemoke no deguchi. Appuru Shuppansha, 1987.

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Edo-zoshi: Kanemoto Nobuo shashinshu = Edo-zoshi, image of ukiyoe, now. Kyoto Shoin, 1987.

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Book chapters on the topic "Kanemite"

1

Burzo, E. "8.1.5.15 Kanemite and ekanite groups and related silicates." In Landolt-Börnstein - Group III Condensed Matter, 579–635. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-71211-4_8.

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Martins, G. A. V., and H. O. Pastore. "The synthesis of SAPO-44 from lamellar ALPO-kanemite." In Molecular Sieves: From Basic Research to Industrial Applications, Proceedings of the 3rd International Zeolite Symposium (3rd FEZA), 335–42. Elsevier, 2005. http://dx.doi.org/10.1016/s0167-2991(05)80357-x.

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Albuquerque, A., S. Coluccia, L. Marchese, and H. O. Pastore. "Synthesis of sapo-34 from the lamellar alpo-kanemite." In Studies in Surface Science and Catalysis, 966–70. Elsevier, 2004. http://dx.doi.org/10.1016/s0167-2991(04)80911-x.

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INAGAKI, S., Y. PUKUSHIMA, A. OKADA, T. KURAUCHI, K. KURODA, and C. KATO. "NEW SILICA-ALUMINA WITH NANO-SCALE PORES PREPARED FROM KANEMITE." In Proceedings from the Ninth International Zeolite Conference, 305–11. Elsevier, 1993. http://dx.doi.org/10.1016/b978-1-4832-8383-8.50035-0.

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Oliveira, Vaeudo Valdimiro de. "THE SUCCESSFUL INCORPORATION OF COPPER IN THE WELL-STRUCTURED SILICATE KANEMITE." In Ciência e Engenharia de Materiais: conceitos, fundamentos e aplicação, 392–409. Editora Científica Digital, 2021. http://dx.doi.org/10.37885/210705415.

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Kooli, F., Y. Kiyozumi, M. Salou, and F. Mizukami. "Formation of new microporous silica phase in protonated kanemite-TMAOH-water system." In Studies in Surface Science and Catalysis, 255–62. Elsevier, 2002. http://dx.doi.org/10.1016/s0167-2991(02)80036-2.

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Kimura, T., H. Tamura, M. Tezuka, D. Mochizuki, T. Shigeno, and K. Kuroda. "Structural design in the silicate framework of ordered mesoporous silica derived from kanemite." In From Zeolites to Porous MOF Materials - The 40th Anniversary of International Zeolite Conference, Proceedings of the 15th International Zeolite Conference, 1740–47. Elsevier, 2007. http://dx.doi.org/10.1016/s0167-2991(07)81054-8.

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Milanesio, M., G. Croce, A. Frache, L. Marchese, D. Viterbo, C. E. da Silva, E. C. Oliveira, and H. O. Pastore. "The transformation of lamellar AlPO-kanemite into chabazite-type CAL-1 3D molecular sieve: a structural study." In Molecular Sieves: From Basic Research to Industrial Applications, Proceedings of the 3rd International Zeolite Symposium (3rd FEZA), 311–18. Elsevier, 2005. http://dx.doi.org/10.1016/s0167-2991(05)80354-4.

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Keene, Matthew T. J., James A. Knowles, and Michael J. Hudson. "The Extraction of the Hexamminecobalt(III) Cation by Kanemite (NaH[Si 2 O 4 (OH) 2 ]·2H 2 O): Enhanced Extraction in the Presence of a Cationic Surfactant." In Progress in Ion Exchange, 412–20. Elsevier, 1997. http://dx.doi.org/10.1533/9781845698652.5.412.

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"2. Kanemi PCB Contamination." In Toxic Politics, 17–57. Cornell University Press, 2020. http://dx.doi.org/10.7591/9781501737602-003.

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