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MY'STORY

The MOVE Fire

This is a personal recollection on the Move fire on May 13, 1985 Philadelphia police fired thousands of rounds at the MOVE house, city officials approved dropping an explosive device on the roof, the resulting fire was allowed to burn, 11 people—including five children—died, and 61 homes were destroyed. Philadelphia City Council later called it a “brutal attack carried out by the City of Philadelphia on its own citizens” and acknowledged that no individual faced criminal consequences for the bombing. One timeline correction worth preserving for the BHP record: the major previous MOVE-police confrontation was August 8, 1978, about seven years before the bombing, not a year or two earlier. Officer James Ramp was killed, other police and firefighters were wounded, nine MOVE members were later convicted, and television cameras recorded police beating Delbert Africa during his arrest. The 1985 MOVE Commission later specifically criticized city planners for failing to adequately use lessons from that 1978 confrontation. And that actually strengthens the point you’re making: 1985 did not happen without precedent or institutional memory. There had already been a deadly confrontation with MOVE, years of conflict, negotiations and police involvement before Osage Avenue.

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BLACK FACTS
The Truths They Never Taught You...

Katherine Johnson — Mathematics to the Moon

Katherine Johnson’s mathematical calculations helped guide some of America’s most important early space missions while she confronted the racial and gender barriers faced by Black women in twentieth-century America.

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BHP gathered finds from its connected research sources. Showing the 4 strongest Black History matches.
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Wikipedia

State variable

A state variable is one of the set of mathematical variables that are used to describe the "state" of a system, e.g. of a dynamical system or a thermodynamical system.

Intuitively, the state of a system is the minimum amount of information about the system which is required to describe the present properties of the system (at least from a certain point of view within a modelling decision of defining a system and separating the system from its environment; if a family of systems is modelled, where the systems are distinguished by parameters, then these parameters are usually not considered to be state variables for the systems, but external system parameters. E.g. physical masses or physical coupling constants for describing interaction strength are given external system parameters, but not state variables for the system.)[1]

In the mathematical model, bounded observables are often taken to be elements of an algebra of observables.[2] Namely, if bounded observables, whose values might be added and multiplied, are modelled by using self-adjoint elements from a Cstar_algebra, then a state is a normalized positive element of the algebra's dual (a continuous linear functional ρ): If the system is in a state , then an observable provides an observed value . (The brackets denote the duality pairing between the dual space of the algebra and the algebra itself.) For example, if the observable is a function from state space to real numbers, then evaluating the function at a point provides a state with , which is the point evaluation functional at point x. In this description, bounded state functions are certain bounded observables. It is possible to extend that notion to unbounded observables (examples in physics: a position component for full space, or a momentum component)[3] for the general abstract case and therefore for more general unbounded state functions. Often, a maximal set of compatible commuting and independent observables can be chosen, and other compatible observables expressed as functions of these observables; then one has made a choice to express all compatible observables as functions of the independent observables, which become independent state variables.

For the definition and examples of states of a thermodynamic system see Thermodynamic state.

In thermodynamics, state variables are physically defined as large-scale characteristics or aggregate properties of a system which provide a macroscopic description of its states.[4][5] In general, state variables have the following properties in common:

  • They don't involve any special assumptions concerning the structure of matter, fields or radiation.
  • They are few in number needed to describe the system.
  • They are fundamental, as suggested by our sensory perceptions.
  • They can be, in general, directly measured.[4]

Classical algebras of observables are abelian[disambiguation needed] (commutative), whereas algebras of quantum observables are Non-Abelian.[6]

The macroscopic thermodynamic description of microscopic quantum systems is obtained as a Thermodynamic Limit of the microscopic system, and a corresponding algebra of observables is obtained, which allows for a definition of macroscopic observables. A distinction between abstract macroscopic observables and observables as thermodynamic state functions can be obtained as follows: For a specific macroscopic state, one uses the GNS-representation to obtain a representation of the algebra of observables as linear operators on a Hilbert space, one chooses a maximally Abelian algebra of compatible observables and applies the Gelfand transform for Abelian C*-algebras to represent abstract observables as functions on a representation space of states (Gelfand space). In general, such a description as functions on a Gelfand space depends on the macroscopic state chosen and is therefore representation dependent. State equations establish certain relations between these functions and therefore might define a variety of states as a set defined by equations for variables. Often, this variety is finite dimensional and then can be described by choosing certain observable state functions as independent state variables and express the other state functions as functions of these independent variables. In this sense, the independent state variables are used to parametrize the variety of states as functions from their domain to the variety of states, whereas general state functions are functions from the set of states to real (or complex) numbers. Composing these functions expresses the values of general observables as functions of the independent state variables, which makes them dependent state variables.

For instance, by describing a thermodynamic system by using the canonical ensemble of microscopic systems in the thermodynamic limit provides independent state variables (temperature, volume, particle number) corresponding to the formula for the thermodynamic free energy with S = entropy, E = internal energy, μ = chemical potential. All other state variables can then be expressed as functions of T,V,N: For a monatomic ideal gas, the state equation for the pressure is the ideal gas law and pressure becomes a dependent state variable, the equation for entropy is the Sackur-Tetrode equation, internal energy can be obtained by requiring Joule's second law, and the chemical potential is computed via the Gibbs potential as described in the section Thermodynamic potentials of the article ideal gas.

All these variables depend only on the states, not on the history of how that state was obtained. This is an important property which makes them state variables, to be distinguished from e.g. process variables (better: process quantities), for which one cannot speak of attaining a particular value when the system is in a state. See the Non-Examples section below.

In the theory of Dynamical Systems, dynamical models that consist of coupled first-order differential equations are said to be in state-variable form.[7]

Examples

[edit]

Non-Examples

[edit]
  • In thermodynamics, heat is not a state variable. No system stores heat.[8] One cannot speak of "the present amount of heat of a system". Heat is a process variable, which describes modes of transfer of energy when the system changes its state. Being a Process_function, heat depends on the process of how the system changes, not only on the system's state currently attained.
  • In thermodynamics, mechanical or thermodynamic work is not a state variable. Work is another mode of transfer of energy when the system changes its state.

Control systems engineering

[edit]

In control engineering and other areas of science and engineering, state variables are used to represent the states of a general system. The set of possible combinations of state variable values is called the state space of the system. The equations relating the current state of a system to its most recent input and past states are called the state equations, and the equations expressing the values of the output variables in terms of the state variables and inputs are called the output equations. As shown below, the state equations and output equations for a linear time invariant system can be expressed using coefficient matrices: A, B, C, and D

where N, L and M are the dimensions of the vectors describing the state, input and output, respectively.

Discrete-time systems

[edit]

The state vector (vector of state variables) representing the current state of a discrete-time system (i.e. digital system) is , where n is the discrete point in time at which the system is being evaluated. The discrete-time state equations are

which describes the next state of the system (x[n+1]) with respect to current state and inputs u[n] of the system. The output equations are

which describes the output y[n] with respect to current states and inputs u[n] to the system.

Continuous time systems

[edit]

The state vector representing the current state of a continuous-time system (i.e. analog system) is , and the continuous-time state equations giving the evolution of the state vector are

which describes the continuous rate of change of the state of the system with respect to current state x(t) and inputs u(t) of the system. The output equations are

which describes the output y(t) with respect to current states x(t) and inputs u(t) to the system.

See also

[edit]

References

[edit]
  1. ^ Ludwig, Günther (1979). Einführung in die Grundlagen der Theoretischen Physik: Band 4: Makrosysteme, Physik und Mensch. Wiesbaden s.l: Vieweg+Teubner Verlag Imprint: Vieweg+Teubner Verlag. ISBN 978-3-663-12070-4.
  2. ^ Emch, Gérard G. (2009). Algebraic methods in statistical mechanics and quantum field theory. Mineola, NY: Dover Publ. ISBN 978-0-486-47209-6.
  3. ^ "Operators and Representation Theory". Dover Publications. Retrieved 2026-06-07.
  4. ^ a b Zemansky, Mark Waldo; Dittman, Richard (1997). Heat and thermodynamics: an intermediate textbook (7th ed.). New York: McGraw-Hill. ISBN 978-0-07-017059-9.
  5. ^ Sewell, Geoffrey L. (2014). Quantum theory of collective phenomena (Dover ed.). Mineola, New York: Dover Publications, Inc. ISBN 978-0-486-78044-3.
  6. ^ Thirring, Walter E. (2002). Quantum mathematical physics: atoms, molecules and large systems (2nd ed.). Berlin ; New York: Springer. ISBN 978-3-540-43078-0.
  7. ^ Palm, III William J. (2009). System Dynamics (2nd ed.). McGraw-Hill Medical Publishing. p. 420. ISBN 978-0-07-126779-3.
  8. ^ Beretta, Gian Paolo; Gyftopoulos, Elias P. (2015-03-01). "What is Heat?". Journal of Energy Resources Technology. 137 (2) 021006. doi:10.1115/1.4026382. ISSN 0195-0738.

Source: Wikipedia. Article content is retrieved live through the MediaWiki API.

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Wikipedia

State variable

A state variable is one of the set of mathematical variables that are used to describe the "state" of a system, e.g. of a dynamical system or a thermodynamical system. Intuitively, the state of a system is the minimum amount of information about the system which is required to describe the present properties of the system (at least from a certain point of view within a modelling decision of defining a system and separating the system from its environment; if a family of systems is modelled, where the systems are distinguished by parameters, then these parameters are usually not considered to be state variables for the systems, but external system parameters. E.g. physical masses or physical coupling constants for describing interaction strength are given external system parameters, but not state variables for the system.) In the mathematical model, bounded observables are often taken to be elements of an algebra of observables. Namely, if bounded observables, whose values might be added and multiplied, are modelled by using self-adjoint elements from a Cstar_algebra, then a state is a normalized positive element of the algebra's dual (a continuous linear functional ρ): If the system is in a state ρ {\textstyle \rho } , then an observable A {\textstyle A} provides an observed value ρ ( A ) =< ρ , A > {\textstyle \rho (A)=} . (The brackets < . , . > {\textstyle } denote the duality pairing between the dual space of the algebra and the algebra itself.) For example, if the observable is a function f {\textstyle f} from state space to real numbers, then evaluating the function at a point x {\textstyle x} provides a state ρ x {\textstyle \rho _{x}} with < ρ x , f >= f ( x ) {\textstyle =f(x)} , which is the point evaluation functional at point x. In this description, bounded state functions are certain bounded observables. It is possible to extend that notion to unbounded observables (examples in physics: a position component for full space, or a momentum component) for the general abstract case and therefore for more general unbounded state functions. Often, a maximal set of compatible commuting and independent observables can be chosen, and other compatible observables expressed as functions of these observables; then one has made a choice to express all compatible observables as functions of the independent observables, which become independent state variables. For the definition and examples of states of a thermodynamic system see Thermodynamic state. In thermodynamics, state variables are physically defined as large-scale characteristics or aggregate properties of a system which provide a macroscopic description of its states. In general, state variables have the following properties in common: They don't involve any special assumptions concerning the structure of matter, fields or radiation. They are few in number needed to describe the system. They are fundamental, as suggested by our sensory perceptions. They can be, in general, directly measured. Classical algebras of observables are abelian (commutative), whereas algebras of quantum observables are Non-Abelian. The macroscopic thermodynamic description of microscopic quantum systems is obtained as a Thermodynamic Limit of the microscopic system, and a corresponding algebra of observables is obtained, which allows for a definition of macroscopic observables. A distinction between abstract macroscopic observables and observables as thermodynamic state functions can be obtained as follows: For a specific macroscopic state, one uses the GNS-representation to obtain a representation of the algebra of observables as linear operators on a Hilbert space, one chooses a maximally Abelian algebra of compatible observables and applies the Gelfand transform for Abelian C*-algebras to represent abstract observables as functions on a representation space of states (Gelfand space). In general, such a description as functions on a Gelfand space depends on the macroscopic state chosen and is therefore representation dependent. State equations establish certain relations between these functions and therefore might define a variety of states as a set defined by equations for variables. Often, this variety is finite dimensional and then can be described by choosing certain observable state functions as independent state variables and express the other state functions as functions of these independent variables. In this sense, the independent state variables are used to parametrize the variety of states as functions from their domain to the variety of states, whereas general state functions are functions from the set of states to real (or complex) numbers. Composing these functions expresses the values of general observables as functions of the independent state variables, which makes them dependent state variables. For instance, by describing a thermodynamic system by using the canonical ensemble of microscopic systems in the thermodynamic limit provides independent state variables T , V , N {\displaystyle T,V,N} (temperature, volume, particle number) corresponding to the formula d F = − S d T − p d V − μ d N {\displaystyle dF=-SdT-pdV-\mu dN} for the thermodynamic free energy F = E − T S {\displaystyle F=E-TS} with S = entropy, E = internal energy, μ = chemical potential. All other state variables can then be expressed as functions of T,V,N: For a monatomic ideal gas, the state equation for the pressure is the ideal gas law and pressure becomes a dependent state variable, the equation for entropy is the Sackur-Tetrode equation, internal energy can be obtained by requiring Joule's second law, and the chemical potential is computed via the Gibbs potential as described in the section Thermodynamic potentials of the article ideal gas. All these variables depend only on the states, not on the history of how that state was obtained. This is an important property which makes them state variables, to be distinguished from e.g. process variables (better: process quantities), for which one cannot speak of attaining a particular value when the system is in a state. See the Non-Examples section below. In the theory of Dynamical Systems, dynamical models that consist of coupled first-order differential equations are said to be in state-variable form.

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Wikipedia

State variable filter

A state variable filter (SVF) is a type of active filter in electronic circuits. In a state-variable filter architecture the signal and its successive derivatives are treated as the core state variables of the system. In state variable filters parameters like gain, cutoff frequency and Q can be independently controlled. This makes it, for example, possible to build a tunable filter where the cutoff frequency is adjustable, while the gain and Q remain constant. A state variable filter consists of one or more integrators, connected in some feedback configuration. It is essentially used when a precise Q factor is required, as other multi-order filters are unable to provide. The most common implementation sums the input signal with its integral and its double integral. State variable filters can also be classified as Multiple Feedback (MFB) and Multi Feedback Loop (MFL) Filters because of the typical feedback configurations. The multiple feedback architecture contributes to the reduced sensitivity to component values of state variable filters.

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Wikipedia

State function

In the thermodynamics of equilibrium, a state function, function of state, or point function for a thermodynamic system is a function relating several state variables or state quantities (that describe equilibrium states of a system) that depend only on the current equilibrium thermodynamic state of the system (e.g. gas, liquid, solid, crystal, or emulsion), not the path which the system has taken to reach that state. A state function describes equilibrium states of a system, thus also describing the type of system. A state variable is typically a state function so the determination of other state variable values at an equilibrium state also determines the value of the state variable as the state function at that state. The ideal gas law is a good example. In this law, one state variable (e.g., pressure, volume, temperature, or the amount of substance in a gaseous equilibrium system) is a function of other state variables so is regarded as a state function. A state function could also describe the number of a certain type of atoms or molecules in a gaseous, liquid, or solid form in a heterogeneous or homogeneous mixture, or the amount of energy required to create such a system or change the system into a different equilibrium state. Internal energy, enthalpy, and entropy are examples of state quantities or state functions because they quantitatively describe an equilibrium state of a thermodynamic system, regardless of how the system has arrived in that state. They are expressed by exact differentials. In contrast, mechanical work and heat are process quantities or path functions because their values depend on a specific "transition" (or "path") between two equilibrium states that a system has taken to reach the final equilibrium state, being expressed by inexact differentials. Exchanged heat (in certain discrete amounts) can be associated with changes of state function such as enthalpy. The description of the system heat exchange is done by a state function, and thus enthalpy changes point to an amount of heat. This can also apply to entropy when heat is compared to temperature. The description breaks down for quantities exhibiting hysteresis.

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Wikipedia

Steady state (chemistry)

In chemistry, a steady state is a situation in which all state variables are constant in spite of ongoing processes that strive to change them. For an entire system to be at steady state, i.e. for all state variables of a system to be constant, there must be a flow through the system (compare mass balance). A simple example of such a system is the case of a bathtub with the tap running but with the drain unplugged: after a certain time, the water flows in and out at the same rate, so the water level (the state variable Volume) stabilizes and the system is in a steady state. The steady state concept is different from chemical equilibrium. Although both may create a situation where a concentration does not change, in a system at chemical equilibrium, the net reaction rate is zero (products transform into reactants at the same rate as reactants transform into products), while no such limitation exists in the steady state concept. Indeed, there does not have to be a reaction at all for a steady state to develop. The term steady state is also used to describe a situation where some, but not all, of the state variables of a system are constant. For such a steady state to develop, the system does not have to be a flow system. Therefore, such a steady state can develop in a closed system where a series of chemical reactions take place. Literature in chemical kinetics usually refers to this case, calling it steady state approximation. In simple systems the steady state is approached by state variables gradually decreasing or increasing until they reach their steady state value. In more complex systems state variables might fluctuate around the theoretical steady state either forever (a limit cycle) or gradually coming closer and closer. It theoretically takes an infinite time to reach steady state, just as it takes an infinite time to reach chemical equilibrium. Both concepts are, however, frequently used approximations because of the substantial mathematical simplifications these concepts offer. Whether or not these concepts can be used depends on the error the underlying assumptions introduce. So, even though a steady state, from a theoretical point of view, requires constant drivers (e.g. constant inflow rate and constant concentrations in the inflow), the error introduced by assuming steady state for a system with non-constant drivers may be negligible if the steady state is approached fast enough (relatively speaking).

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TOPIC OF THE DAY

Greenwood / Black Wall Street

Before the 1921 destruction of Tulsa’s Greenwood District, Black residents had created a remarkable center of business and community life. The district included stores, professional offices, entertainment venues and homes owned by Black citizens. Understanding Greenwood means learning what was built—not only what was burned.

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TRIVIA QUESTION OF THE DAY

Which Black woman became the first elected to the United States Congress?

Shirley Chisholm, elected in 1968.