Patent classifications
C08F22/22
DENTAL MILL BLANK
The present invention provides a dental mill blank having an excellent mechanical strength and an excellent water resistance according to which a decrease in mechanical strength can be suppressed even in an environment where water is present, for example, inside an oral cavity. The present invention relates to a dental mill blank including: a polymer (A); and continuous inorganic fibers (B) that are oriented substantially in one direction, wherein the dental mill blank has a decreasing rate of 40% or less in three-point flexural strength after immersion in 70° C. water for seven days.
DENTAL MILL BLANK
The present invention provides a dental mill blank having an excellent mechanical strength and an excellent water resistance according to which a decrease in mechanical strength can be suppressed even in an environment where water is present, for example, inside an oral cavity. The present invention relates to a dental mill blank including: a polymer (A); and continuous inorganic fibers (B) that are oriented substantially in one direction, wherein the dental mill blank has a decreasing rate of 40% or less in three-point flexural strength after immersion in 70° C. water for seven days.
OPTICAL ELEMENT, OPTICAL APPARATUS, IMAGING APPARATUS, AND COMPOUND
An optical element containing a cured product of a resin composition containing a compound represented by the formula (1):
##STR00001## wherein X.sub.1 denotes a substituted phenyl group with at least one trifluoromethyl group and is optionally substituted with a hydrogen atom, C1-C4 alkyl group, and/or C1-C3 alkylene group, X.sub.2 denotes a substituted or unsubstituted phenyl group, A denotes at least one of a substituted or unsubstituted phenyl group and a substituted or unsubstituted biphenyl group, the substituted phenyl group of X.sub.2 and the substituted phenyl group and the substituted biphenyl group of A have at least one of a hydrogen atom, trifluoromethyl group, C1-C4 alkyl group, and C1-C3 alkylene group, and P.sub.1, P.sub.2, and P.sub.3 denote an acryloyloxy group or a methacryloyloxy group, a, b, and c denote an integer of 0 to 2, and a+b+c denotes an integer of 1 to 3.
OPTICAL ELEMENT, OPTICAL APPARATUS, IMAGING APPARATUS, AND COMPOUND
An optical element containing a cured product of a resin composition containing a compound represented by the formula (1):
##STR00001## wherein X.sub.1 denotes a substituted phenyl group with at least one trifluoromethyl group and is optionally substituted with a hydrogen atom, C1-C4 alkyl group, and/or C1-C3 alkylene group, X.sub.2 denotes a substituted or unsubstituted phenyl group, A denotes at least one of a substituted or unsubstituted phenyl group and a substituted or unsubstituted biphenyl group, the substituted phenyl group of X.sub.2 and the substituted phenyl group and the substituted biphenyl group of A have at least one of a hydrogen atom, trifluoromethyl group, C1-C4 alkyl group, and C1-C3 alkylene group, and P.sub.1, P.sub.2, and P.sub.3 denote an acryloyloxy group or a methacryloyloxy group, a, b, and c denote an integer of 0 to 2, and a+b+c denotes an integer of 1 to 3.
Chloride-free cationic polymers using acetate anions
A composition contains ethylenically unsaturated quaternary ammonium cations with acetate counterions, where each of the ethylenically unsaturated ammonium cations contain only one non-aromatic carbon-carbon double bond and the composition contains less than one mole-percent chloride relative to quaternary ammonium cations can be polymerized to form a cationic polymer acetate.
Chloride-free cationic polymers using acetate anions
A composition contains ethylenically unsaturated quaternary ammonium cations with acetate counterions, where each of the ethylenically unsaturated ammonium cations contain only one non-aromatic carbon-carbon double bond and the composition contains less than one mole-percent chloride relative to quaternary ammonium cations can be polymerized to form a cationic polymer acetate.
Photocurable compositions for stereolithography, method of forming the compositions, stereolithography methods using the compositions, polymer components formed by the stereolithography methods, and a device including the polymer components
A photocurable composition for stereolithographic three-dimensional printing, wherein the photocurable composition comprises a photoreactive oligomer component comprising a hydrophobic oligomer comprising a photoreactive end group, a photoreactive monomer component comprising a photoreactive monomer having a photoreactive end group, and a photoinitiation composition comprising a photoinitiator; the photocurable composition has a viscosity of 250 to 10,000 centipoise at 22° C., determined using a Brookfield viscometer; and the photocured composition has a dielectric loss of less than 0.010, preferably less than 0.008, more preferably less than 0.006, most preferably less than 0.004, each determined by split-post dielectric resonator testing at 10 gigahertz at 23° C.
Photocurable compositions for stereolithography, method of forming the compositions, stereolithography methods using the compositions, polymer components formed by the stereolithography methods, and a device including the polymer components
A photocurable composition for stereolithographic three-dimensional printing, wherein the photocurable composition comprises a photoreactive oligomer component comprising a hydrophobic oligomer comprising a photoreactive end group, a photoreactive monomer component comprising a photoreactive monomer having a photoreactive end group, and a photoinitiation composition comprising a photoinitiator; the photocurable composition has a viscosity of 250 to 10,000 centipoise at 22° C., determined using a Brookfield viscometer; and the photocured composition has a dielectric loss of less than 0.010, preferably less than 0.008, more preferably less than 0.006, most preferably less than 0.004, each determined by split-post dielectric resonator testing at 10 gigahertz at 23° C.
POLYMER SOLID ELECTROLYTES, METHODS OF MAKING, AND ELECTROCHEMICAL CELLS COMPRISING THE SAME
Disclosed are various polymer solid electrolyte materials suitable for various electrochemical devices and methods for making or using the same. The polymer solid electrolyte comprises a crosslinked polymer from a polymer. Certain embodiments are generally directed to solid electrolytes having relatively high ionic conductivity and/or other mechanical or electrical properties, e.g., tensile strength or decomposition potential. Certain aspects include a polymer, a plasticizer, and an electrolyte salt. In some cases, the polymer for synthesizing the crosslinked polymer may exhibit certain structures such as:
##STR00001##
where R.sub.1 can be one of the following groups:
##STR00002##
where n is an integer between 1 and 10000, m is an integer between 1 and 5000, and R.sub.2 to R.sub.6 can each independently be one:
##STR00003##
selected from the group consisting of hydrogen, methyl, ethyl, phenyl, benzyl, acryl, epoxy ethyl, isocyanate, cyclic carbonate, lactone, lactam, and vinyl; and * indicates a point of attachment.
POLYMER SOLID ELECTROLYTES, METHODS OF MAKING, AND ELECTROCHEMICAL CELLS COMPRISING THE SAME
Disclosed are various polymer solid electrolyte materials suitable for various electrochemical devices and methods for making or using the same. The polymer solid electrolyte comprises a crosslinked polymer from a polymer. Certain embodiments are generally directed to solid electrolytes having relatively high ionic conductivity and/or other mechanical or electrical properties, e.g., tensile strength or decomposition potential. Certain aspects include a polymer, a plasticizer, and an electrolyte salt. In some cases, the polymer for synthesizing the crosslinked polymer may exhibit certain structures such as:
##STR00001##
where R.sub.1 can be one of the following groups:
##STR00002##
where n is an integer between 1 and 10000, m is an integer between 1 and 5000, and R.sub.2 to R.sub.6 can each independently be one:
##STR00003##
selected from the group consisting of hydrogen, methyl, ethyl, phenyl, benzyl, acryl, epoxy ethyl, isocyanate, cyclic carbonate, lactone, lactam, and vinyl; and * indicates a point of attachment.