A manufacturing method for a moisture permeable device suitable for use in a refrigerator where the device includes a corresponding first surface (110) and second surface (111); at least parts of the first surface (110) and the second surface (111) of the moisture permeable device define a hollow cavity (301); through-holes are provided at regions of the first surface (110) and the second surface (111) of the moisture permeable device defining the cavity (301); and regenerated cellulose is accommodated in the cavity (301) includes the steps of pouring a regenerated cellulose slurry with a tackifier added thereto into the cavity (301) to form a moisture permeable film, thus allowing omission of an assembling procedure and a non-woven support.

A wearable disinfecting device includes a skin-protective glove and a disinfecting material. The disinfecting material is attached to the external surface on the palm side of the skin-protective glove. The disinfecting material includes an absorbent material that is at least partially saturated with a disinfecting liquid. The skin-protective glove is chemically resistant to the disinfecting liquid. A protective film that covers the disinfecting material can be releasably attached to the external surface of the skin-protective glove.

A wearable disinfecting device includes a skin-protective glove and a disinfecting material. The disinfecting material is attached to the external surface on the palm side of the skin-protective glove. The disinfecting material includes an absorbent material that is at least partially saturated with a disinfecting liquid. The skin-protective glove is chemically resistant to the disinfecting liquid. A protective film that covers the disinfecting material can be releasably attached to the external surface of the skin-protective glove.

The present disclosure belongs to the technical field of analytical chemistry, in particular to synthesis and application of a nanomaterial for removal of patulin (Pat). The present disclosure adopts 2-Oxin as a substitute template, AM as a functional monomer, and synthetic Fe.sub.3O4@SiO.sub.2@CS-GO magnetic nanoparticles as a carrier, for preparing a magnetic MIP specific for Pat adsorption by surface imprinting. The addition of Fe.sub.3O.sub.4 makes the finally prepared molecular imprinted adsorbent material magnetic, thereby facilitating separation of a material from a matrix, eliminating complicated operation steps such as filtration and centrifugation, and facilitating recovery of materials.

The present disclosure belongs to the technical field of analytical chemistry, in particular to synthesis and application of a nanomaterial for removal of patulin (Pat). The present disclosure adopts 2-Oxin as a substitute template, AM as a functional monomer, and synthetic Fe.sub.3O4@SiO.sub.2@CS-GO magnetic nanoparticles as a carrier, for preparing a magnetic MIP specific for Pat adsorption by surface imprinting. The addition of Fe.sub.3O.sub.4 makes the finally prepared molecular imprinted adsorbent material magnetic, thereby facilitating separation of a material from a matrix, eliminating complicated operation steps such as filtration and centrifugation, and facilitating recovery of materials.

A product, a method of producing and a method of using are disclosed. The product comprises attapulgite that has been thermally activated. The product may have a permeability in oil in the range of 0.04-3 darcy and may have a surface area of 45-140 m.sup.2/g. The method of producing may comprise thermally activating a material that includes attapulgite by heating the material at a temperature in the range of 300 to 900° C. The method of decolorizing may include contacting for a contact time an oil with the bleaching clay product that comprises attapulgite that has been thermally activated, and separating the bleaching clay product from the oil to recover a decolorized oil that has a lower red color than the oil had prior to the contacting, and removing phosphorus and metals for hydrotreated vegetable oil (HVO)/renewable diesel feedstock pretreatment.

A product, a method of producing and a method of using are disclosed. The product comprises attapulgite that has been thermally activated. The product may have a permeability in oil in the range of 0.04-3 darcy and may have a surface area of 45-140 m.sup.2/g. The method of producing may comprise thermally activating a material that includes attapulgite by heating the material at a temperature in the range of 300 to 900° C. The method of decolorizing may include contacting for a contact time an oil with the bleaching clay product that comprises attapulgite that has been thermally activated, and separating the bleaching clay product from the oil to recover a decolorized oil that has a lower red color than the oil had prior to the contacting, and removing phosphorus and metals for hydrotreated vegetable oil (HVO)/renewable diesel feedstock pretreatment.

Lime-based sorbent suitable for use in a flue gas treatment process comprising at least 70 wt. % of Ca(OH).sub.2 and at least 0.2 wt. % to at most 10 wt. % of a first additive selected among the group of hydrogels of natural or synthetic origin, in particular superabsorbent polymers (SAPs) or in the group of cellulose ethers or a combination thereof, premix for use in a manufacturing process of said sorbent, process for manufacturing the sorbent and use of said sorbent in a flue gas treatment process

Lime-based sorbent suitable for use in a flue gas treatment process comprising at least 70 wt. % of Ca(OH).sub.2 and at least 0.2 wt. % to at most 10 wt. % of a first additive selected among the group of hydrogels of natural or synthetic origin, in particular superabsorbent polymers (SAPs) or in the group of cellulose ethers or a combination thereof, premix for use in a manufacturing process of said sorbent, process for manufacturing the sorbent and use of said sorbent in a flue gas treatment process

The present invention relates to a lectin-macromolecular carrier coupling complex for separating glycosylated exosomes from a clinical sample, which comprises a macromolecular carrier and lectins coupled to the outer side of the macromolecular carrier. The complex may simply, conveniently, rapidly, and accurately separate glycosylated exosomes from a clinical sample with a high separation efficiency and a good repeatability; and the separated exosomes are intact in morphology without rupturing or cracking, may be directly used for liquid detection of glycosylated exosomes, or directly used for immunology-related detection, or directly used for gene detection or analysis after extracting related nucleic acids from the exosomes.