Patent classifications
C01B39/22
PROCESS FOR SYNTHESIZING ZEOLITE CRYSTALS WITH SEEDING AGENT
The present invention relates to process for synthesizing zeolite X crystals comprising at least one step of adding seeding agent(s) into a synthesis gel and at least one step of forming zeolite X crystals at a temperature strictly greater than 120 C., preferably equal to or greater than 130 C.
PROCESS FOR SYNTHESIZING ZEOLITE CRYSTALS WITH SEEDING AGENT
The present invention relates to process for synthesizing zeolite X crystals comprising at least one step of adding seeding agent(s) into a synthesis gel and at least one step of forming zeolite X crystals at a temperature strictly greater than 120 C., preferably equal to or greater than 130 C.
Silver-carrying zeolite molded article
Provided are: a silver-carrying zeolite molded article in which aggregation of silver is inhibited and which has excellent capability of dispersing silver, when compared to conventional silver-carrying zeolite molded articles; and a method for producing the silver-carrying zeolite molded article. In the silver-carrying zeolite molded article, the molar ratio of Si/Al.sub.2 is 2.0-3.0, the molar ratio of (alkali metal+Ag)/Al is 0.9-1.1, the total amount of SiO.sub.2, Al.sub.2O.sub.3, Ag.sub.2O, and alkali metal oxides is 90 wt % or more, the contained amount of silver ions is 5 wt % or more, and only a single type of zeolite is contained. The molded article can be produced by subjecting a zeolite molded article having zeolite purity of 90% or more to an ion exchange treatment using a silver-containing aqueous solution.
Silver-carrying zeolite molded article
Provided are: a silver-carrying zeolite molded article in which aggregation of silver is inhibited and which has excellent capability of dispersing silver, when compared to conventional silver-carrying zeolite molded articles; and a method for producing the silver-carrying zeolite molded article. In the silver-carrying zeolite molded article, the molar ratio of Si/Al.sub.2 is 2.0-3.0, the molar ratio of (alkali metal+Ag)/Al is 0.9-1.1, the total amount of SiO.sub.2, Al.sub.2O.sub.3, Ag.sub.2O, and alkali metal oxides is 90 wt % or more, the contained amount of silver ions is 5 wt % or more, and only a single type of zeolite is contained. The molded article can be produced by subjecting a zeolite molded article having zeolite purity of 90% or more to an ion exchange treatment using a silver-containing aqueous solution.
Methods for preparing LiCa-LSX molecular sieves with mixed cations and applications thereof
The present invention relates to a method for preparing LiCa-LSX molecular sieves with mixed cations and applications thereof. The method comprises the following steps; preparing CaLSX molecular sieves; replacing all Na.sup.+ in NaLSX molecular sieves with Ca.sup.2+ by multiple times of exchange with a solution containing Ca.sup.2+; changing CaLSX molecular sieves to LiCa-LSX molecular sieves by exchange with Li.sup.+, wherein a solution containing Li.sup.+ is used, and the exchanged sample is directly filtered in vacuum without washing and dried at normal temperature; and activating and pre-treating the sample to obtain LiCa-LSX molecular sieves with mixed cations. The LiCa-LSX molecular sieves can be used as selective adsorbents for N.sub.2 and O.sub.2 in oxygen production processes by PSA/VPSA. In the present invention, the loss of Li.sup.+ caused by the replacement of Li.sup.+ with H.sup.+ because of hydrolysis is avoided, the cost is reduced and the treatment time is short.
Methods for preparing LiCa-LSX molecular sieves with mixed cations and applications thereof
The present invention relates to a method for preparing LiCa-LSX molecular sieves with mixed cations and applications thereof. The method comprises the following steps; preparing CaLSX molecular sieves; replacing all Na.sup.+ in NaLSX molecular sieves with Ca.sup.2+ by multiple times of exchange with a solution containing Ca.sup.2+; changing CaLSX molecular sieves to LiCa-LSX molecular sieves by exchange with Li.sup.+, wherein a solution containing Li.sup.+ is used, and the exchanged sample is directly filtered in vacuum without washing and dried at normal temperature; and activating and pre-treating the sample to obtain LiCa-LSX molecular sieves with mixed cations. The LiCa-LSX molecular sieves can be used as selective adsorbents for N.sub.2 and O.sub.2 in oxygen production processes by PSA/VPSA. In the present invention, the loss of Li.sup.+ caused by the replacement of Li.sup.+ with H.sup.+ because of hydrolysis is avoided, the cost is reduced and the treatment time is short.
PROCESS FOR CONTINUOUSLY SYNTHESIZING ZEOLITE CRYSTALS
The present invention relates to a process for preparing zeolite crystals continuously, comprising the continuous introduction of a composition capable of generating zeolite crystals into at least one crystallization reaction zone subjected to stirring means, giving said composition a flow characterized by a relative Reynolds number Re.sub.r of between 40 and 50 000, and the continuous recovery of the crystals formed according to a flow characterized by a net Reynolds number Re.sub.n of between 1 and 1500.
Heavy metal adsorbent, water purification material, and method of manufacturing heavy metal adsorbent
Provided is a heavy metal adsorbent consisting of a zeolite with a median diameter on a volume basis of 10.0 ?m or more and a pore volume measured in a pore volume calculation range of 10 nm to 1000 nm by a mercury intrusion method of 0.1000 cm.sup.3/g or less.
Heavy metal adsorbent, water purification material, and method of manufacturing heavy metal adsorbent
Provided is a heavy metal adsorbent consisting of a zeolite with a median diameter on a volume basis of 10.0 ?m or more and a pore volume measured in a pore volume calculation range of 10 nm to 1000 nm by a mercury intrusion method of 0.1000 cm.sup.3/g or less.
HEAVY METAL ADSORBENT, WATER PURIFICATION MATERIAL, AND METHOD OF MANUFACTURING HEAVY METAL ADSORBENT
Provided is a heavy metal adsorbent consisting of a zeolite with a median diameter on a volume basis of 10.0 ?m or more and a pore volume measured in a pore volume calculation range of 10 nm to 1000 nm by a mercury intrusion method of 0.1000 cm.sup.3/g or less.